ClinVar Miner

List of variants in gene CYP21A2, LOC106780800, LOC110631417 studied for adrenocortical insufficiency

Included ClinVar conditions (20):

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.-113G>A	rs1246774295	0.00251
NM_000500.9(CYP21A2):c.17TGC[6] (p.Leu10dup)	rs61338903
NM_000500.9(CYP21A2):c.[-4C>T;1360C>T317C>T]

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