ClinVar Miner

List of variants in gene combination CYP21A2, LOC106780800 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.1174G>A (p.Ala392Thr)	rs202242769	0.00567
NM_000500.9(CYP21A2):c.49C>T (p.Arg17Cys)	rs757608533	0.00001
NM_000500.9(CYP21A2):c.293-13C>A	rs6467

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