ClinVar Miner

List of variants in gene ARHGEF6 reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_004840.2(ARHGEF6):c.-232G>A rs183947764
NM_004840.3(ARHGEF6):c.*131_*134del rs775186031
NM_004840.3(ARHGEF6):c.*1531C>T rs181090402
NM_004840.3(ARHGEF6):c.*158A>G rs112837910
NM_004840.3(ARHGEF6):c.*176G>A rs745563328
NM_004840.3(ARHGEF6):c.*179C>T rs146018376
NM_004840.3(ARHGEF6):c.*1817dup rs751450350
NM_004840.3(ARHGEF6):c.*197_*199GTT[1] rs770569536
NM_004840.3(ARHGEF6):c.*2021A>G rs151143657
NM_004840.3(ARHGEF6):c.*2062T>C rs142057050
NM_004840.3(ARHGEF6):c.*2082T>G rs144027474
NM_004840.3(ARHGEF6):c.*2346C>T rs41312580
NM_004840.3(ARHGEF6):c.*2469C>T rs189644416
NM_004840.3(ARHGEF6):c.*38C>T rs747771125
NM_004840.3(ARHGEF6):c.*545C>T rs182548859
NM_004840.3(ARHGEF6):c.1190C>G (p.Thr397Ser) rs532348958
NM_004840.3(ARHGEF6):c.1446T>C (p.Ser482=) rs775489071
NM_004840.3(ARHGEF6):c.166-11T>C rs140322310
NM_004840.3(ARHGEF6):c.169T>C (p.Cys57Arg) rs147131853
NM_004840.3(ARHGEF6):c.362G>A (p.Arg121His) rs35106300
NM_004840.3(ARHGEF6):c.685G>A (p.Val229Ile) rs75329154

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