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
共济失调性毛细血管扩张症
共济失调性毛细血管扩张症
发起讨论
共济失调性毛细血管扩张症
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
共济失调性毛细血管扩张症
0 个讨论
相关基因
ATM
位点：RS121434219
位点：RS377349459
位点：RS532480170
位点：RS587776551
位点：RS1137887
位点：RS138941496
位点：RS139770721
位点：RS587778077
位点：RS587778080
位点：RS587779813
位点：RS587779815
位点：RS587779818
位点：RS587779833
位点：RS587779872
位点：RS587780639
位点：RS587781302
位点：RS587781363
位点：RS587781511
位点：RS587781722
位点：RS587781823
位点：RS587781894
位点：RS587781911
位点：RS587781950
位点：RS587781967
位点：RS587782103
位点：RS587782114
位点：RS587782192
位点：RS587782292
位点：RS587782652
位点：RS587782719
位点：RS730881309
位点：RS730881333
位点：RS730881336
位点：RS730881369
位点：RS730881384
位点：RS730881388
位点：RS747727055
位点：RS748634900
位点：RS752135143
位点：RS762083530
位点：RS764389018
位点：RS768362387
位点：RS769142993
位点：RS772821016
位点：RS777849257
位点：RS780619951
位点：RS786201689
位点：RS786201693
位点：RS786201957
位点：RS786202743
位点：RS786202826
位点：RS786203054
位点：RS786203606
位点：RS786203888
位点：RS786204433
位点：RS786204726
位点：RS796051858
位点：RS797045030
位点：RS863224462
位点：RS864622490
位点：RS876658163
位点：RS876658740
位点：RS876660382
位点：RS876660485
位点：RS876660741
位点：RS876660842
位点：RS876660933
位点：RS879254093
BRAF
位点：RS121913376
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