ClinVar Miner

List of variants in gene combination SCNN1A, TNFRSF1A reported as likely benign for autosomal recessive pseudohypoaldosteronism type 1

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_001065.3(TNFRSF1A):c.-233C>T rs45537340
NM_001065.3(TNFRSF1A):c.-74G>A rs200084924
NM_001065.3(TNFRSF1A):c.-96C>T rs115164694

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