ClinVar Miner

List of variants in gene RAD50 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.2903G>A (p.Gly968Glu) rs199895166 0.00017
NM_005732.4(RAD50):c.259C>T (p.Arg87Cys) rs143802516 0.00014
NM_005732.4(RAD50):c.2840T>C (p.Ile947Thr) rs150401251 0.00009
NM_005732.4(RAD50):c.2750C>T (p.Thr917Ile) rs562172843 0.00005
NM_005732.4(RAD50):c.3230G>A (p.Arg1077Gln) rs104895051 0.00005
NM_005732.4(RAD50):c.281T>C (p.Ile94Thr) rs768127412 0.00004
NM_005732.4(RAD50):c.625G>C (p.Glu209Gln) rs587780158 0.00004
NM_005732.4(RAD50):c.695C>A (p.Ala232Asp) rs28903089 0.00004
NM_005732.4(RAD50):c.1970-7A>C rs370034340 0.00003
NM_005732.4(RAD50):c.2718+10T>G rs765764447 0.00003
NM_005732.4(RAD50):c.785T>G (p.Leu262Arg) rs201728859 0.00003
NM_005732.4(RAD50):c.129+5G>A rs587781409 0.00001
NM_005732.4(RAD50):c.1353T>A (p.Ser451Arg) rs587782523 0.00001
NM_005732.4(RAD50):c.2092A>G (p.Ile698Val) rs781213977 0.00001
NM_005732.4(RAD50):c.2502G>C (p.Glu834Asp) rs377438445 0.00001
NM_005732.4(RAD50):c.3206G>T (p.Arg1069Ile) rs769003601 0.00001
NM_005732.4(RAD50):c.1287A>G (p.Ile429Met) rs1554098314
NM_005732.4(RAD50):c.1794-9T>C rs1060504397
NM_005732.4(RAD50):c.1930A>G (p.Arg644Gly) rs876659631
NM_005732.4(RAD50):c.2693T>G (p.Val898Gly) rs1750958706
NM_005732.4(RAD50):c.2829+7T>C
NM_005732.4(RAD50):c.670C>T (p.Arg224Cys) rs753136372
NM_005732.4(RAD50):c.677A>C (p.Gln226Pro) rs1060501953
NM_005732.4(RAD50):c.699G>T (p.Gln233His) rs755911947
NM_005732.4(RAD50):c.973T>C (p.Cys325Arg) rs863224744

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