ClinVar Miner

List of variants in gene RAD50 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.551+123T>C rs2522403 0.34048
NM_005732.4(RAD50):c.1246-136T>C rs2706362 0.33292
NM_005732.4(RAD50):c.365+227G>C rs2522414 0.32073
NM_005732.4(RAD50):c.3165-335C>T rs7449456 0.23652
NM_005732.4(RAD50):c.3164+174T>C rs2301713 0.23190
NM_005732.4(RAD50):c.1246-149A>C rs56798121 0.18026
NM_005732.4(RAD50):c.551+19G>A rs17166050 0.17902
NM_005732.4(RAD50):c.3165-252A>G rs17772583 0.17894
NM_005732.4(RAD50):c.1793+313T>C rs10463893 0.16617
NM_005732.4(RAD50):c.2524+166T>G rs12187537 0.15819
NM_005732.4(RAD50):c.1453-118G>A rs2706364 0.13006
NM_005732.4(RAD50):c.1246-210A>G rs2706360 0.12814
NM_005732.4(RAD50):c.2525-157G>A rs2522391 0.07447
NM_005732.4(RAD50):c.3036+242T>C rs2706378 0.07447
NM_005732.4(RAD50):c.2398-115A>G rs2706377 0.07442
NM_005732.4(RAD50):c.3036+33C>T rs10054336 0.05656
NM_005732.4(RAD50):c.3389+154A>G rs140257448 0.05188
NM_005732.4(RAD50):c.366-295T>C rs13360175 0.05180
NM_005732.4(RAD50):c.1453-278C>A rs17166060 0.04384
NM_005732.4(RAD50):c.1453-203C>G rs10520117 0.04382
NM_005732.4(RAD50):c.1969+30A>C rs2522390 0.03078
NM_005732.4(RAD50):c.3164+140A>G rs74426446 0.02953
NM_005732.4(RAD50):c.551+85A>G rs75639632 0.02708
NM_005732.4(RAD50):c.2025C>T (p.Asp675=) rs34147298 0.02660
NM_005732.4(RAD50):c.3389+96T>C rs59635188 0.02658
NM_005732.4(RAD50):c.214-44G>A rs74769721 0.02590
NM_005732.4(RAD50):c.1052-38C>T rs104895045 0.01852
NM_005732.4(RAD50):c.2718+131C>T rs112364014 0.01774
NM_005732.4(RAD50):c.1793+22T>C rs10520116 0.01080
NM_005732.4(RAD50):c.1245+23T>C rs115100130 0.00716
NM_005732.4(RAD50):c.1246-42T>A rs114648433 0.00706
NM_005732.4(RAD50):c.3037-3T>C rs115737081 0.00627
NM_005732.4(RAD50):c.572C>T (p.Thr191Ile) rs2230017 0.00469
NM_005732.4(RAD50):c.2910C>T (p.Asp970=) rs148269640 0.00422
NM_005732.4(RAD50):c.1051+58A>T rs77502957 0.00256
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091 0.00207
NM_005732.4(RAD50):c.379G>A (p.Val127Ile) rs28903086 0.00146
NM_005732.4(RAD50):c.1052-6del rs201800554
NM_005732.4(RAD50):c.129+184T>C rs2548986
NM_005732.4(RAD50):c.129+236C>A rs73257757
NM_005732.4(RAD50):c.1453-131del rs138231496
NM_005732.4(RAD50):c.1636-9del rs762814289
NM_005732.4(RAD50):c.2719-178G>A rs2522394
NM_005732.4(RAD50):c.2923-5dup rs2066742
NM_005732.4(RAD50):c.3164+250= rs4705961
NM_005732.4(RAD50):c.432T>G (p.Leu144=) rs181804987

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