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視網膜色素變性
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視網膜色素變性
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E3/E3為什么是10.34倍？
能喝的TUSC3基因
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相關基因
RHO
位點：RS104893791
RP2
位點：RS104894927
USH2A
位點：RS111033385
位點：RS121912600
位點：RS375668376
位點：RS397517964
位點：RS397517973
位點：RS397517989
位點：RS397517990
位點：RS397518003
位點：RS397518008
位點：RS397518011
位點：RS397518014
位點：RS397518021
位點：RS397518036
位點：RS397518041
位點：RS397518048
位點：RS398124619
位點：RS527236137
位點：RS753330544
位點：RS727505337
位點：RS372347027
位點：RS201657446
位點：RS727503731
位點：RS397517963
位點：RS111033280
位點：W01216380743
BBS2
位點：RS121908175
位點：RS121908179
HGSNAT
位點：RS121908285
位點：RS756310864
位點：RS775078211
NR2E3
位點：RS121912631
位點：RS28937873
位點：RS786205493
RPE65
位點：RS121917745
位點：RS62653011
位點：RS61752883
位點：RS61752902
位點：RS62642584
PANK2
位點：RS137852959
位點：RS863223343
KLHL7
位點：RS137853113
CRB1
位點：RS137853137
位點：RS62635655
位點：RS62636267
位點：RS786205450
位點：RS863223341
RLBP1
位點：RS137853290
SNRNP200
位點：RS267607077
位點：RS786205529
POMGNT1
位點：RS28940869
位點：RS386834039
MYO7A
位點：RS35689081
CNGB1
位點：RS372504780
CC2D2A
位點：RS386833750
位點：RS386833760
C8orf37
位點：RS387907136
ABCA4
位點：RS61751399
位點：RS62654395
位點：RS61751402
位點：RS61748558
位點：RS61749420
位點：RS61750137
位點：RS61750564
位點：RS61751389
位點：RS61752401
位點：RS61753046
位點：RS62645944
位點：RS786205447
位點：RS886044758
PRPH2
位點：RS61755806
AIPL1
位點：RS62637014
EYS
位點：RS794727631
位點：RS184722374
位點：RS372354156
位點：RS752683070
位點：RS797045089
AHI1
位點：RS372659908
位點：RS797045224
RPGR
位點：RS62640589
CNGA1
位點：RS759781200
IMPG2
位點：RS763295314
位點：RS786205564
SPATA7
位點：RS767745816
MERTK
位點：RS786205533
位點：RS786205535
CERKL
位點：RS786205545
NRL
位點：RS794727281
RBBP9
位點：RS797044735
位點：RS863223340
PDE6B
位點：RS876657718
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
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<center id="gqcfk"></center>
<p id="gqcfk"></p>
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純合片段分析
姓氏祖源
祖源平均臉
基因關系
基因保險助手
原始數據
深圳市市場監督管理局企業主體身份公示
中文
English