List of variants in gene XRCC2 reported as uncertain significance for Fanconi anemia, complementation group U

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: 13

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HGVS	dbSNP
NM_005431.2(XRCC2):c.181C>A (p.Leu61Ile)	rs569810249
NM_005431.2(XRCC2):c.229G>C (p.Glu77Gln)	rs142527605
NM_005431.2(XRCC2):c.283A>G (p.Ile95Val)	rs140214637
NM_005431.2(XRCC2):c.374_377ACTT[1] (p.Leu126fs)	rs763401560
NM_005431.2(XRCC2):c.596T>C (p.Met199Thr)	rs149099078
NM_005431.2(XRCC2):c.608C>T (p.Ser203Leu)	rs143856570
NM_005431.2(XRCC2):c.613T>G (p.Ser205Ala)	rs56103026
NM_005431.2(XRCC2):c.620A>G (p.Glu207Gly)	rs61762969
NM_005431.2(XRCC2):c.643C>T (p.Arg215Ter)	rs143153871
NM_005431.2(XRCC2):c.644G>A (p.Arg215Gln)	rs762828701
NM_005431.2(XRCC2):c.698A>T (p.Gln233Leu)	rs946075316
NM_005431.2(XRCC2):c.714G>C (p.Arg238Ser)	rs534746330
NM_005431.2(XRCC2):c.794T>C (p.Leu265Ser)	rs771671971

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