ClinVar Miner

List of variants in gene SCNN1G reported as uncertain significance for Liddle syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001039.4(SCNN1G):c.*1147A>G rs80081880
NM_001039.4(SCNN1G):c.*584G>A rs886051802
NM_001039.4(SCNN1G):c.*789_*790delinsCT rs386789797
NM_001039.4(SCNN1G):c.1083G>A (p.Glu361=) rs752432261
NM_001039.4(SCNN1G):c.1187A>G (p.His396Arg) rs202142122
NM_001039.4(SCNN1G):c.1378A>G (p.Lys460Glu) rs886051801
NM_001039.4(SCNN1G):c.1550T>C (p.Met517Thr) rs144653364
NM_001039.4(SCNN1G):c.446G>C (p.Gly149Ala) rs754747376
NM_001039.4(SCNN1G):c.538C>T (p.Arg180Trp) rs763601481
NM_001039.4(SCNN1G):c.663G>T (p.Ser221=) rs886051800
NM_001039.4(SCNN1G):c.776C>A (p.Thr259Asn) rs72646501

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