ClinVar Miner

List of variants in gene combination CYP11A1, LOC108964933 reported as uncertain significance for Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency

Included ClinVar conditions (1):

Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000781.3(CYP11A1):c.-59A>G	rs567971184	0.00007
NM_000781.3(CYP11A1):c.-35A>G	rs886051481

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