List of variants reported as uncertain significance for Gitelman syndrome by Revvity Omics, Revvity

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.1561A>G (p.Ile521Val)	rs147046379	0.00175
NM_001126108.2(SLC12A3):c.1648G>A (p.Ala550Thr)	rs563131364	0.00031
NM_001126108.2(SLC12A3):c.2793C>T (p.Asn931=)	rs13306666	0.00006
NM_001126108.2(SLC12A3):c.1919A>G (p.Asn640Ser)	rs886039754	0.00001
NM_001126108.2(SLC12A3):c.1914C>G (p.Ile638Met)	rs749234287
NM_001126108.2(SLC12A3):c.2273T>C (p.Ile758Thr)	rs61730207
NM_001126108.2(SLC12A3):c.575T>C (p.Ile192Thr)
NM_001126108.2(SLC12A3):c.704C>T (p.Thr235Met)

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