ClinVar Miner

List of variants in gene SLC6A8 reported as likely 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: 20
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HGVS dbSNP
NM_005629.3(SLC6A8):c.1146G>A (p.Pro382=) rs782627741
NM_005629.3(SLC6A8):c.1218C>T (p.Phe406=) rs1557045310
NM_005629.3(SLC6A8):c.1284C>T (p.Gly428=) rs781788160
NM_005629.3(SLC6A8):c.1290C>T (p.Leu430=) rs782667574
NM_005629.3(SLC6A8):c.1414C>T (p.Leu472=) rs781974297
NM_005629.3(SLC6A8):c.1452C>G (p.Leu484=) rs376421364
NM_005629.3(SLC6A8):c.1515C>T (p.Asp505=) rs151335200
NM_005629.3(SLC6A8):c.1570T>A (p.Ser524Thr) rs782703394
NM_005629.3(SLC6A8):c.1597-4G>A rs1312663828
NM_005629.3(SLC6A8):c.1614C>T (p.Asn538=) rs369726574
NM_005629.3(SLC6A8):c.1653C>T (p.Tyr551=) rs369715906
NM_005629.3(SLC6A8):c.1714G>A (p.Val572Met) rs2872524
NM_005629.3(SLC6A8):c.1719G>A (p.Pro573=) rs2314070
NM_005629.3(SLC6A8):c.1767+15C>T rs370331295
NM_005629.3(SLC6A8):c.1768-9C>G rs782234529
NM_005629.3(SLC6A8):c.42C>T (p.Ser14=) rs1060504719
NM_005629.3(SLC6A8):c.644+8C>T rs782433720
NM_005629.3(SLC6A8):c.644+9G>A rs200353790
NM_005629.3(SLC6A8):c.87G>C (p.Gly29=) rs782373793
NM_005629.3(SLC6A8):c.93G>A (p.Pro31=) rs782197450

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