使用本网站需要启用 JavaScript, 请启用后刷新页面获得更好的体验
登录
注册
首页
个人基因检测
临床应用研究
科研合作项目
合作与服务
社区
纯合片段分析
姓氏祖源
祖源平均脸
基因关系
基因保险助手
原始数据
使用 WeGene 需要启用 Cookies, 请启用后刷新页面获得更好的体验
社区首页
小组
Fanconi 贫血
Fanconi 贫血
发起讨论
Fanconi 贫血
0 个讨论
只看精华帖
按热门排序
按最新排序
暂时没有精华内容
发起讨论
Fanconi 贫血
0 个讨论
相关基因
FANCC
位点：RS104886456
位点：RS1057516291
位点：RS730881709
位点：RS730881731
位点：RS769039987
位点：RS878853671
PALB2
位点：RS118203998
位点：RS180177092
位点：RS180177100
位点：RS180177122
位点：RS180177126
位点：RS180177132
位点：RS180177133
位点：RS180177135
位点：RS180177143
位点：RS587776527
位点：RS730881876
位点：RS878855122
FANCG
位点：RS149616199
位点：RS397507560
位点：RS786204205
位点：RS863224506
RAD51C
位点：RS200293302
位点：RS267606997
位点：RS267606999
位点：RS387907159
位点：RS587781287
位点：RS587781995
位点：RS587782528
位点：RS587782702
位点：RS587782818
位点：RS730881931
位点：RS730881940
位点：RS759292615
位点：RS767796996
位点：RS770637624
位点：RS786201909
位点：RS876659874
BRCA1
位点：RS273897655
位点：RS273899698
位点：RS397508838
位点：RS41293465
位点：RS62625307
位点：RS80356885
位点：RS80356898
位点：RS80357063
位点：RS80357104
位点：RS80357233
位点：RS80357346
位点：RS80357350
位点：RS80357440
位点：RS80357727
位点：RS80357906
位点：RS80357970
位点：RS80358079
位点：RS879255498
BRCA2
位点：RS28897743
位点：RS28897756
位点：RS397507327
位点：RS397507409
位点：RS397508045
位点：RS398122783
位点：RS80358435
位点：RS80358620
位点：RS80358695
位点：RS80358721
位点：RS80358809
位点：RS80359014
位点：RS80359035
位点：RS80359070
位点：RS80359180
位点：RS80359200
位点：RS80359212
位点：RS80359405
位点：RS80359479
位点：RS80359520
位点：RS80359550
位点：RS80359607
位点：RS80359770
位点：RS80359429
FANCA
位点：RS397507552
位点：RS148100796
位点：RS747851434
位点：RS780825099
位点：RS786204204
FANCI
位点：RS375656231
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
纯合片段分析
姓氏祖源
祖源平均脸
基因关系
基因保险助手
原始数据
深圳市市场监督管理局企业主体身份公示
中文
English