List of variants in gene XRCC2 reported as likely pathogenic for anemia

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_005431.2(XRCC2):c.643C>T (p.Arg215Ter)	rs143153871	0.00006
NM_005431.2(XRCC2):c.350dup (p.Leu117fs)	rs764640893
NM_005431.2(XRCC2):c.378_381del (p.Leu126fs)	rs763401560

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