ClinVar Miner

List of variants in gene SCNN1G reported as pathogenic for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_001039.4(SCNN1G):c.1718G>A (p.Trp573Ter) rs137853342
NM_001039.4(SCNN1G):c.1749_1753del (p.Glu583fs) rs1567270184
NM_001039.4(SCNN1G):c.318-1G>A rs1567262640
SCNN1G, 1-BP DEL, 1627G
SCNN1G, ASN530SER
SCNN1G, GLN567TER
SCNN1G, IVS11, G-A, -1

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