ClinVar Miner

List of variants in gene SLC12A3 reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001126108.2(SLC12A3):c.791C>G (p.Ala264Gly) rs1529927 0.97710
NM_001126108.2(SLC12A3):c.1670-8T>C rs2304483 0.48985
NM_001126108.2(SLC12A3):c.2924+13C>T rs2289115 0.34518
NM_001126108.2(SLC12A3):c.2721-13T>C rs34772420 0.18153
NM_001126108.2(SLC12A3):c.1395C>T (p.Thr465=) rs5801 0.15318
NM_001126108.2(SLC12A3):c.2857-17G>A rs2289116 0.13711
NM_001126108.2(SLC12A3):c.2142C>T (p.Ala714=) rs5803 0.11388
NM_001126108.2(SLC12A3):c.2179-8C>T rs13306676 0.11191
NM_001126108.2(SLC12A3):c.2598C>T (p.Gly866=) rs5804 0.09125
NM_001126108.2(SLC12A3):c.2711G>A (p.Arg904Gln) rs11643718 0.08381
NM_001126108.2(SLC12A3):c.1884G>A (p.Ser628=) rs5802 0.08069
NM_001126108.2(SLC12A3):c.366A>G (p.Ala122=) rs2304479 0.05592
NM_001126108.2(SLC12A3):c.1825+9C>A rs35797045 0.03711
NM_001126108.2(SLC12A3):c.2755C>T (p.Arg919Cys) rs12708965 0.03475
NM_001126108.2(SLC12A3):c.1444-17G>A rs71387142 0.03307
NM_001126108.2(SLC12A3):c.2182G>A (p.Ala728Thr) rs36049418 0.01075
NM_001126108.2(SLC12A3):c.36C>T (p.Asp12=) rs117987946 0.00061

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