ClinVar Miner

List of variants in gene XRCC2 reported as benign for not provided

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.39+202C>T rs2106776 0.46605
NC_000007.14:g.152676167C>G rs3218384 0.17037
NM_005431.2(XRCC2):c.*183C>T rs3218541 0.06488
NC_000007.14:g.152676148A>C rs3218385 0.06216
NC_000007.14:g.152676331G>A rs3218382 0.05380
NM_005431.2(XRCC2):c.39+310G>C rs3218387 0.05164
NM_005431.2(XRCC2):c.*1T>C rs3218539 0.04983
NM_005431.2(XRCC2):c.563G>A (p.Arg188His) rs3218536 0.04933
NM_005431.2(XRCC2):c.121+158T>G rs3218475 0.02370
NM_005431.2(XRCC2):c.40-10C>T rs3218472 0.01055
NM_005431.2(XRCC2):c.*40G>C rs3218540 0.00902
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.354G>A (p.Val118=) rs558977371 0.00012
NM_005431.2(XRCC2):c.678T>C (p.Tyr226=) rs143357617 0.00010
NM_005431.2(XRCC2):c.477C>T (p.Arg159=) rs202226401 0.00008
NM_005431.2(XRCC2):c.39+8C>G rs200363289 0.00006
NM_005431.2(XRCC2):c.300A>G (p.Leu100=) rs146700851 0.00001
NM_005431.2(XRCC2):c.390T>G (p.Leu130=) rs752735963 0.00001
NM_005431.2(XRCC2):c.*227_*228del rs10707642
NM_005431.2(XRCC2):c.*228del rs10707642
NM_005431.2(XRCC2):c.121+3dup rs1064794394
NM_005431.2(XRCC2):c.40-6dup
NM_005431.2(XRCC2):c.726C>T (p.Ser242=) rs2116987114
NM_005431.2(XRCC2):c.825T>C (p.Ser275=) rs770438650

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