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
Download table as spreadsheet
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.