ClinVar Miner

List of variants in gene LTBR, SCNN1A studied 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: 7
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HGVS dbSNP
NM_001038.6(SCNN1A):c.-55+2T>C
NM_001038.6(SCNN1A):c.-55+5G>C rs13306617
NM_001038.6(SCNN1A):c.-69C>T rs545108113
NM_001038.6(SCNN1A):c.-93A>G rs10849447
NM_001270987.2(LTBR):c.39+11C>T rs72645137
NM_001270987.2(LTBR):c.39+12G>A rs72645138
NM_001270987.2(LTBR):c.39+42G>A rs72645139

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