ClinVar Miner

List of variants reported as likely benign for Gitelman syndrome by Natera, Inc.

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001126108.2(SLC12A3):c.307C>T (p.Leu103=) rs35005216 0.00257
NM_001126108.2(SLC12A3):c.1980C>T (p.Asp660=) rs201519016 0.00185
NM_001126108.2(SLC12A3):c.1561A>G (p.Ile521Val) rs147046379 0.00175
NM_001126108.2(SLC12A3):c.1392C>A (p.Ala464=) rs118121751 0.00146
NM_001126108.2(SLC12A3):c.2190C>T (p.Leu730=) rs150692587 0.00146
NM_001126108.2(SLC12A3):c.93C>T (p.Pro31=) rs34055681 0.00143
NM_001126108.2(SLC12A3):c.1284C>T (p.Thr428=) rs34216426 0.00098
NM_001126108.2(SLC12A3):c.2028C>T (p.His676=) rs35070204 0.00073
NM_001126108.2(SLC12A3):c.36C>T (p.Asp12=) rs117987946 0.00061
NM_001126108.2(SLC12A3):c.1698C>A (p.Asn566Lys) rs757776621 0.00038
NM_001126108.2(SLC12A3):c.1453G>A (p.Glu485Lys) rs201804135 0.00011
NM_001126108.2(SLC12A3):c.1710G>A (p.Ala570=) rs387907471 0.00008
NM_001126108.2(SLC12A3):c.1932G>A (p.Gln644=) rs749222099 0.00006
NM_001126108.2(SLC12A3):c.2793C>T (p.Asn931=) rs13306666 0.00006
NM_001126108.2(SLC12A3):c.1956C>A (p.Pro652=) rs200091201 0.00004
NM_001126108.2(SLC12A3):c.2514C>T (p.Asp838=) rs142297310 0.00004
NM_001126108.2(SLC12A3):c.348G>A (p.Gly116=) rs149890322 0.00003
NM_001126108.2(SLC12A3):c.2172C>T (p.Leu724=) rs201038360 0.00001
NM_001126108.2(SLC12A3):c.2397C>T (p.Asp799=) rs139943829 0.00001
NM_001126108.2(SLC12A3):c.2673T>C (p.His891=) rs769641982 0.00001
NM_001126108.2(SLC12A3):c.2076C>T (p.Ile692=) rs780880719
NM_001126108.2(SLC12A3):c.2285+10_2285+12del rs562443353

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