ClinVar Miner

List of variants in gene SLC12A6 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_001365088.1(SLC12A6):c.*3097G>C rs4238571 0.96869
NM_001365088.1(SLC12A6):c.*1492T>C rs6495640 0.95051
NM_001365088.1(SLC12A6):c.*1047A>G rs4780233 0.61133
NM_001365088.1(SLC12A6):c.3003C>T (p.Leu1001=) rs4577050 0.60784
NM_001365088.1(SLC12A6):c.*3403G>A rs4530104 0.57931
NM_001365088.1(SLC12A6):c.475C>T (p.Leu159=) rs7164902 0.22884
NM_001365088.1(SLC12A6):c.*2637A>G rs59712831 0.16772
NM_001365088.1(SLC12A6):c.1551G>C (p.Pro517=) rs17236798 0.16144
NM_001365088.1(SLC12A6):c.1236G>A (p.Ser412=) rs2290940 0.16143
NM_001365088.1(SLC12A6):c.*494A>G rs16958873 0.15870
NM_001365088.1(SLC12A6):c.*2804C>T rs59091709 0.11152
NM_001365088.1(SLC12A6):c.*3525C>T rs1133154 0.11134
NM_001365088.1(SLC12A6):c.*1846C>G rs6495639 0.10640
NM_001365088.1(SLC12A6):c.1825-13C>T rs74010036 0.10170
NM_001365088.1(SLC12A6):c.*2523C>T rs191826889 0.06232
NM_001365088.1(SLC12A6):c.*824T>C rs75307067 0.06174
NM_001365088.1(SLC12A6):c.*3668T>A rs11544435 0.02645
NM_001365088.1(SLC12A6):c.*1098G>A rs117846663 0.02253
NM_001365088.1(SLC12A6):c.2934+12G>C rs11854257 0.02091
NM_001365088.1(SLC12A6):c.963C>T (p.Tyr321=) rs35583475 0.01718
NM_001365088.1(SLC12A6):c.*1725G>A rs76243307 0.01650
NM_001365088.1(SLC12A6):c.*2659A>G rs142451941 0.01079
NM_001365088.1(SLC12A6):c.1284C>T (p.Asn428=) rs34098566 0.00816
NM_001365088.1(SLC12A6):c.2925G>A (p.Val975=) rs112835706 0.00711
NM_001365088.1(SLC12A6):c.1269C>T (p.Tyr423=) rs114911287 0.00588
NM_001365088.1(SLC12A6):c.318C>T (p.Asp106=) rs116086579 0.00575
NM_001365088.1(SLC12A6):c.*2369C>T rs148928495 0.00563
NM_001365088.1(SLC12A6):c.2935-7A>G rs184053916 0.00465
NM_001365088.1(SLC12A6):c.1752A>C (p.Gly584=) rs186888172 0.00067
NM_001365088.1(SLC12A6):c.*1087C>A rs4779660

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