ClinVar Miner

List of variants in gene HERC1 reported as uncertain significance for premature menopause

Included ClinVar conditions (10):

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003922.4(HERC1):c.4931T>C (p.Ile1644Thr)	rs746301906	0.00005
NM_003922.4(HERC1):c.8236A>G (p.Thr2746Ala)	rs769159645

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