List of variants in gene XRCC2 reported as likely benign for immune system disorder

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.808T>G (p.Phe270Val)	rs145085742	0.00205
NM_005431.2(XRCC2):c.40-16T>C	rs41274991	0.00141
NM_005431.2(XRCC2):c.39+8C>G	rs200363289	0.00006

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