ClinVar Miner

List of variants in gene SLC9A6 reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (163):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_001042537.1(SLC9A6):c.367C>T (p.Pro123Ser) rs587784400
NM_001042537.1(SLC9A6):c.412A>G (p.Ser138Gly) rs587784401
NM_001042537.1(SLC9A6):c.685A>G (p.Ile229Val) rs587784402
NM_006359.2(SLC9A6):c.1376G>A (p.Gly459Asp)
NM_006359.2(SLC9A6):c.1488C>T (p.Gly496=) rs782370742
NM_006359.2(SLC9A6):c.1843A>G (p.Ser615Gly) rs558960349
NM_006359.2(SLC9A6):c.269T>C (p.Leu90Pro) rs1556614843
NM_006359.2(SLC9A6):c.362A>G (p.His121Arg) rs1060502675
NM_006359.2(SLC9A6):c.485A>G (p.Tyr162Cys) rs1556616834
NM_006359.2(SLC9A6):c.619G>A (p.Val207Ile)
NM_006359.2(SLC9A6):c.8G>T (p.Arg3Leu)
NM_006359.2(SLC9A6):c.946G>A (p.Val316Met) rs1556618832

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