List of variants in gene combination LOC126862361, SLC12A3 reported as benign for Familial hypokalemia-hypomagnesemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.*205A>G	rs5805	0.63172
NM_001126108.2(SLC12A3):c.3024C>T (p.Ile1008=)	rs2289113	0.01151
NM_001126108.2(SLC12A3):c.2964G>A (p.Ser988=)	rs35082264	0.00802

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