ClinVar Miner

List of variants in gene CYP11A1, LOC108964933 studied for Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000781.3(CYP11A1):c.-59A>G	rs567971184	0.00005
NM_000781.3(CYP11A1):c.-35A>G	rs886051481

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