ClinVar Miner

List of variants in gene SLC9A6 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=) rs151178361 0.00022
NM_001379110.1(SLC9A6):c.852A>T (p.Ala284=) rs371472909 0.00015
NM_001379110.1(SLC9A6):c.-9G>T rs367724979 0.00009
NM_001379110.1(SLC9A6):c.228T>C (p.Asn76=) rs782529317 0.00006
NM_001379110.1(SLC9A6):c.1005A>G (p.Val335=) rs782706500 0.00004
NM_001379110.1(SLC9A6):c.1833A>T (p.Thr611=) rs782629258 0.00002
NM_001379110.1(SLC9A6):c.1862C>T (p.Pro621Leu) rs782442071 0.00002
NM_001379110.1(SLC9A6):c.1578C>T (p.His526=) rs782430960 0.00001
NM_001379110.1(SLC9A6):c.549G>A (p.Thr183=) rs782386487 0.00001
NM_001379110.1(SLC9A6):c.-43C>T rs1569523768
NM_001379110.1(SLC9A6):c.1938G>A (p.Gly646=)
NM_001379110.1(SLC9A6):c.448-6dup rs375038684
NM_001379110.1(SLC9A6):c.786C>T (p.Thr262=)

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