ClinVar Miner

List of variants in gene SLC9A6 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: 9
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HGVS dbSNP
NM_001042537.1(SLC9A6):c.25G>T (p.Ala9Ser) rs201523857
NM_006359.2(SLC9A6):c.1020C>G (p.Thr340=) rs1060504686
NM_006359.2(SLC9A6):c.1141-8C>T rs1060504684
NM_006359.2(SLC9A6):c.1224C>T (p.Val408=) rs1556619315
NM_006359.2(SLC9A6):c.1668G>A (p.Pro556=) rs1060504687
NM_006359.2(SLC9A6):c.171C>G (p.Ile57Met) rs782296172
NM_006359.2(SLC9A6):c.384T>C (p.Asn128=) rs782529317
NM_006359.2(SLC9A6):c.576C>T (p.Phe192=) rs1423014570
NM_006359.2(SLC9A6):c.663A>G (p.Leu221=) rs1060504685

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