ClinVar Miner

List of variants in gene SLC12A3 reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001126108.2(SLC12A3):c.*664G>C rs5808 0.62518
NM_001126108.2(SLC12A3):c.*931C>T rs37030 0.60253
NM_001126108.2(SLC12A3):c.*1851A>G rs37029 0.60231
NM_001126108.2(SLC12A3):c.*404C>T rs37031 0.58188
NM_001126108.2(SLC12A3):c.*1524C>T rs3812964 0.57598
NM_001126108.2(SLC12A3):c.*516T>A rs11861555 0.49704
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.*1301A>C rs9927820 0.29170
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.2142C>T (p.Ala714=) rs5803 0.11388
NM_001126108.2(SLC12A3):c.2179-8C>T rs13306676 0.11191
NM_001126108.2(SLC12A3):c.*975A>G rs56079121 0.11158
NM_001126108.2(SLC12A3):c.*1674C>T rs3812963 0.09905
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.1023C>T (p.Phe341=) rs2229209 0.04172
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.*1204T>C rs116537640 0.02034
NM_001126108.2(SLC12A3):c.*2432T>C rs115344087 0.02023
NM_001126108.2(SLC12A3):c.1865A>G (p.Asn622Ser) rs61746763 0.01422
NM_001126108.2(SLC12A3):c.*2068C>G rs142540870 0.01329
NM_001126108.2(SLC12A3):c.1539C>T (p.Tyr513=) rs146805986 0.00597
NM_001126108.2(SLC12A3):c.1176C>T (p.Thr392=) rs117440321

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