ClinVar Miner

List of variants in gene XRCC2 studied for Fanconi anemia

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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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.39+8C>G rs200363289
NM_005431.2(XRCC2):c.40-16T>C rs41274991
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
NM_005431.2(XRCC2):c.808T>G (p.Phe270Val) rs145085742

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