List of variants in gene ERCC2 reported as likely pathogenic for female reproductive organ cancer

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000400.4(ERCC2):c.47A>G (p.Tyr16Cys)	rs147972150	0.00125
NM_000400.4(ERCC2):c.1972C>T (p.Arg658Cys)	rs121913021	0.00004
NM_000400.4(ERCC2):c.1559A>G (p.Tyr520Cys)

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