ClinVar Miner

List of variants in gene RB1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_000321.3(RB1):c.500+23T>G rs198617 0.93273
NM_000321.3(RB1):c.501-77A>G rs198616 0.92110
NM_000321.3(RB1):c.1499-182T>A rs2804085 0.91988
NM_000321.3(RB1):c.1695+97T>A rs2804086 0.91986
NM_000321.3(RB1):c.2106+185A>G rs198581 0.91031
NM_000321.3(RB1):c.2663+33C>T rs3020646 0.90292
NM_000321.3(RB1):c.2713+308G>A rs2984828 0.90273
NM_000321.3(RB1):c.2106+136C>T rs9562824 0.89112
NM_000321.3(RB1):c.1961-77G>A rs198580 0.88350
NM_000321.3(RB1):c.1696-277C>T rs198574 0.77217
NM_000321.3(RB1):c.718+312A>T rs198619 0.55756
NM_000321.3(RB1):c.137+107G>A rs2252544 0.55039
NM_000321.3(RB1):c.2106+142del rs377255892 0.26073
NM_000321.3(RB1):c.380+45C>T rs520342 0.21231
NM_000321.3(RB1):c.2106+139T>C rs368843896 0.20964
NM_000321.3(RB1):c.2664-10T>A rs3092904 0.19833
NM_000321.3(RB1):c.381-152A>G rs3092899 0.11650
NM_000321.3(RB1):c.608-3182C>T rs9535021 0.10366
NM_000321.3(RB1):c.1127+74C>T rs3092888 0.07482
NM_000321.3(RB1):c.264+75T>C rs3092865 0.05520
NM_000321.3(RB1):c.1216-230G>T rs4151532 0.05238
NM_000321.3(RB1):c.2106+146del rs370147449 0.05175
NM_000321.3(RB1):c.1390-14A>T rs9535023 0.04866
NM_000321.3(RB1):c.1049+270G>A rs4151502 0.03590
NM_000321.3(RB1):c.540-162T>C rs74075978 0.03583
NM_000321.3(RB1):c.608-3377C>T rs113995265 0.03314
NM_000321.3(RB1):c.608-3569T>C rs77089731 0.03313
NM_000321.3(RB1):c.500+305G>T rs4151460 0.03256
NM_000321.3(RB1):c.264+283T>C rs4151429 0.03246
NM_000321.3(RB1):c.861+505C>G rs4151487 0.03244
NM_000321.3(RB1):c.1215+220G>A rs4151524 0.03175
NM_000321.3(RB1):c.1815-104A>G rs3092898 0.02847
NM_000321.3(RB1):c.1216-29A>G rs3092886 0.02593
NM_000321.3(RB1):c.861+167A>G rs2097211 0.01797
NM_000321.3(RB1):c.380+12T>C rs3092881 0.01087
NM_000321.3(RB1):c.1574C>G (p.Ala525Gly) rs4151539 0.00623
NM_000321.3(RB1):c.2521-11G>A rs4151624 0.00570
NM_000321.3(RB1):c.2490-45A>G rs4151610 0.00540
NM_000321.3(RB1):c.1390-11A>G rs200658795 0.00365
NM_000321.3(RB1):c.920C>T (p.Thr307Ile) rs183898408 0.00079
NM_000321.3(RB1):c.411A>T (p.Glu137Asp) rs3092902 0.00040
NM_000321.3(RB1):c.929G>A (p.Gly310Glu) rs200844292 0.00029
NM_000321.3(RB1):c.1049+58G>A rs3092883
NM_000321.3(RB1):c.1128-72G>T rs185587
NM_000321.3(RB1):c.1333-61dup rs11449461
NM_000321.3(RB1):c.137+86T>C rs2854351
NM_000321.3(RB1):c.138-262G>C rs1981434
NM_000321.3(RB1):c.1389+194del rs3092892
NM_000321.3(RB1):c.1390-168G>C rs2070752
NM_000321.3(RB1):c.1390-17del rs753535084
NM_000321.3(RB1):c.1390-17dup rs753535084
NM_000321.3(RB1):c.1390-70del rs35427721
NM_000321.3(RB1):c.1390-70dup rs35427721
NM_000321.3(RB1):c.1499-57del rs11351399
NM_000321.3(RB1):c.1695+81_1695+82insAA rs4151540
NM_000321.3(RB1):c.2106+111dup rs66565903
NM_000321.3(RB1):c.2106+119_2106+120insCT rs747042227
NM_000321.3(RB1):c.2106+119_2106+120insCTT rs765008765
NM_000321.3(RB1):c.2106+119_2106+120insCTTTCTT rs765008765
NM_000321.3(RB1):c.2106+120_2106+121del rs66738983
NM_000321.3(RB1):c.2106+121del rs66738983
NM_000321.3(RB1):c.2106+122_2106+149del rs1566235830
NM_000321.3(RB1):c.2106+129dup rs374033062
NM_000321.3(RB1):c.2106+146_2106+147insCTTTTT rs10627069
NM_000321.3(RB1):c.2106+68_2106+70del rs1379075407
NM_000321.3(RB1):c.2106+96_2106+147del rs1566235744
NM_000321.3(RB1):c.2212-12G>T rs776987458
NM_000321.3(RB1):c.2212-14C>T rs80122842
NM_000321.3(RB1):c.2212-15A>T rs372815788
NM_000321.3(RB1):c.2212-15_2212-14del rs756296581
NM_000321.3(RB1):c.2489+214G>T rs4151602
NM_000321.3(RB1):c.264+310dup rs11452683
NM_000321.3(RB1):c.265-244_265-237del rs146556286
NM_000321.3(RB1):c.265-9551T>A
NM_000321.3(RB1):c.45_53del (p.Ala16_Ala18del) rs572454921
NM_000321.3(RB1):c.608-144dup rs547128110
NM_000321.3(RB1):c.719-315del rs148037416
NM_000321.3(RB1):c.861+262del rs11332935
NM_000321.3(RB1):c.861+262dup rs11332935
NM_000321.3(RB1):c.862-127del rs144536235

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