ClinVar Miner

List of variants in gene SLC9A6 reported as benign for not specified

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1306+8G>A rs6654310 0.05510
NM_001379110.1(SLC9A6):c.1689C>T (p.Ser563=) rs2307131 0.02758
NM_001379110.1(SLC9A6):c.744-6C>T rs17001258 0.01856
NM_001379110.1(SLC9A6):c.1662-4G>A rs188072063 0.00703
NM_001379110.1(SLC9A6):c.474T>C (p.Ser158=) rs144316388 0.00662
NM_001379110.1(SLC9A6):c.1029A>C (p.Ala343=) rs142049079 0.00390
NM_001379110.1(SLC9A6):c.1460+4A>G rs180727016 0.00239
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln) rs146263125 0.00166
NM_001379110.1(SLC9A6):c.*5_*6del rs781795776 0.00157
NM_001379110.1(SLC9A6):c.*8A>T rs200171451 0.00157
NM_001379110.1(SLC9A6):c.1460+10A>G rs185533973 0.00013
NM_001379110.1(SLC9A6):c.1581+11G>A rs375145994 0.00012
NM_001379110.1(SLC9A6):c.-16C>T rs139299794 0.00003
NM_001379110.1(SLC9A6):c.801G>A (p.Ala267=) rs185192141 0.00001
NM_001379110.1(SLC9A6):c.*5_*8delinsTT rs797044655
NM_001379110.1(SLC9A6):c.1582-3C>T rs563279759
NM_001379110.1(SLC9A6):c.448-6del rs375038684

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