ClinVar Miner

List of variants in gene SLC6A8 reported as benign 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: 29
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HGVS dbSNP
NM_005629.3(SLC6A8):c.-5A>G rs384573
NM_005629.3(SLC6A8):c.1016+10G>A rs371905179
NM_005629.3(SLC6A8):c.1016+9C>T rs190690083
NM_005629.3(SLC6A8):c.1020C>T (p.Asp340=) rs144252036
NM_005629.3(SLC6A8):c.1141+6G>A rs373124777
NM_005629.3(SLC6A8):c.1162G>A (p.Ala388Thr) rs374163604
NM_005629.3(SLC6A8):c.1437C>T (p.Ser479=) rs140115896
NM_005629.3(SLC6A8):c.1473C>T (p.Cys491=) rs122453118
NM_005629.3(SLC6A8):c.1494C>T (p.Tyr498=) rs143916832
NM_005629.3(SLC6A8):c.1496-4G>A rs782589547
NM_005629.3(SLC6A8):c.1496-5C>T rs200695210
NM_005629.3(SLC6A8):c.1496-8C>T rs376038235
NM_005629.3(SLC6A8):c.1597-5C>T rs376073223
NM_005629.3(SLC6A8):c.1626C>T (p.Tyr542=) rs140601882
NM_005629.3(SLC6A8):c.1649C>G (p.Thr550Ser) rs199635059
NM_005629.3(SLC6A8):c.1678A>G (p.Met560Val) rs145438966
NM_005629.3(SLC6A8):c.1713C>T (p.Cys571=) rs782244505
NM_005629.3(SLC6A8):c.1768-3C>T rs150207268
NM_005629.3(SLC6A8):c.1890G>C (p.Val630=) rs376385129
NM_005629.3(SLC6A8):c.495C>T (p.Thr165=) rs144904949
NM_005629.3(SLC6A8):c.498G>A (p.Thr166=) rs201260657
NM_005629.3(SLC6A8):c.544G>A (p.Val182Met) rs149024147
NM_005629.3(SLC6A8):c.777+4C>T rs201581661
NM_005629.3(SLC6A8):c.780C>T (p.Ile260=) rs148232368
NM_005629.3(SLC6A8):c.813C>T (p.Val271=) rs138064933
NM_005629.3(SLC6A8):c.820G>A (p.Val274Met) rs782208622
NM_005629.3(SLC6A8):c.87G>A (p.Gly29=) rs782373793
NM_005629.3(SLC6A8):c.912+9G>A rs782694291
NM_005629.3(SLC6A8):c.975A>C (p.Thr325=) rs782517934

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