ClinVar Miner

List of variants in gene RAB3GAP2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_012414.4(RAB3GAP2):c.3155-194C>G rs141613840 0.02558
NM_012414.4(RAB3GAP2):c.1488-222_1488-221del rs141349027 0.01723
NM_012414.4(RAB3GAP2):c.2416+285T>C rs114769082 0.01258
NM_012414.4(RAB3GAP2):c.812-153C>A rs116370890 0.01257
NM_012414.4(RAB3GAP2):c.812-261G>A rs138829349 0.01246
NM_012414.4(RAB3GAP2):c.2577+266G>A rs2577129 0.01115
NM_012414.4(RAB3GAP2):c.713-72G>A rs114038940 0.00760
NM_012414.4(RAB3GAP2):c.2577+176A>G rs142368719 0.00639
NM_012414.4(RAB3GAP2):c.3867+33C>G rs114940727 0.00612
NM_012414.4(RAB3GAP2):c.2806+181C>T rs185647458 0.00595
NM_012414.4(RAB3GAP2):c.613-207A>C rs137944267 0.00576
NM_012414.4(RAB3GAP2):c.1487+250G>T rs6701106 0.00512
NM_012414.4(RAB3GAP2):c.2578-313A>G rs140779183 0.00506
NM_012414.4(RAB3GAP2):c.1998+331T>C rs186373235 0.00505
NM_012414.4(RAB3GAP2):c.2213-72G>T rs189531804 0.00499
NM_012414.4(RAB3GAP2):c.3556-175T>C rs143324123 0.00484
NM_012414.4(RAB3GAP2):c.3155-141A>G rs113804589 0.00422
NM_012414.4(RAB3GAP2):c.812-276A>G rs112968685 0.00421
NM_012414.4(RAB3GAP2):c.1270+241C>T rs12144630 0.00411
NM_012414.4(RAB3GAP2):c.612+29A>G rs77791948 0.00400
NM_012414.4(RAB3GAP2):c.3155-136A>G rs111713427 0.00394
NM_012414.4(RAB3GAP2):c.1779+7G>A rs111345353 0.00390
NM_012414.4(RAB3GAP2):c.2577+79G>A rs180790267 0.00298
NM_012414.4(RAB3GAP2):c.3966A>G (p.Lys1322=) rs150226729 0.00206
NM_012414.4(RAB3GAP2):c.4060A>G (p.Ile1354Val) rs59190330 0.00174
NM_012414.4(RAB3GAP2):c.39C>T (p.Asp13=) rs145667920 0.00149
NM_012414.4(RAB3GAP2):c.938C>T (p.Thr313Ile) rs74139292 0.00104
NM_012414.4(RAB3GAP2):c.112C>T (p.Pro38Ser) rs138796052 0.00102
NM_012414.4(RAB3GAP2):c.2290C>T (p.Leu764Phe) rs139337049 0.00097
NM_012414.4(RAB3GAP2):c.3390G>A (p.Ala1130=) rs140377995 0.00045
NM_012414.4(RAB3GAP2):c.2168T>A (p.Val723Glu) rs150643803 0.00044
NM_012414.4(RAB3GAP2):c.304+25A>T rs190706082 0.00042
NM_012414.4(RAB3GAP2):c.2807-15G>A rs200407685 0.00038
NM_012414.4(RAB3GAP2):c.2667T>G (p.Leu889=) rs145550355 0.00021
NM_012414.4(RAB3GAP2):c.2212+15A>T rs375627012 0.00013
NM_012414.4(RAB3GAP2):c.33C>G (p.Phe11Leu) rs1446997240 0.00013
NM_012414.4(RAB3GAP2):c.465C>T (p.Cys155=) rs144263040 0.00012
NM_012414.4(RAB3GAP2):c.1281C>T (p.Asp427=) rs372594666 0.00005
NM_012414.4(RAB3GAP2):c.4027-5T>C rs779800010 0.00003
NM_012414.4(RAB3GAP2):c.2008C>G (p.Leu670Val) rs201613456 0.00002
NM_012414.4(RAB3GAP2):c.1092A>G (p.Gln364=) rs772862686 0.00001
NM_012414.4(RAB3GAP2):c.1715-8del rs1297620057 0.00001
NM_012414.4(RAB3GAP2):c.2715C>T (p.Ser905=) rs775564285 0.00001
NM_012414.4(RAB3GAP2):c.2778T>C (p.Ser926=) rs1057523891 0.00001
NM_012414.4(RAB3GAP2):c.3757C>T (p.Pro1253Ser) rs564016323 0.00001
NM_012414.4(RAB3GAP2):c.2311-83T>G rs150060767
NM_012414.4(RAB3GAP2):c.2890G>C (p.Asp964His) rs774456466
NM_012414.4(RAB3GAP2):c.304+12A>G rs530311696
NM_012414.4(RAB3GAP2):c.3154+13A>T rs1248395562
NM_012414.4(RAB3GAP2):c.3154+287del rs71169436
NM_012414.4(RAB3GAP2):c.3261+106G>A rs151021083
NM_012414.4(RAB3GAP2):c.3999C>T (p.Pro1333=) rs539609673
NM_012414.4(RAB3GAP2):c.434+14A>G rs1026065056
NM_012414.4(RAB3GAP2):c.613-24dup rs572027376
NM_012414.4(RAB3GAP2):c.712+12G>T rs530494745
NM_012414.4(RAB3GAP2):c.713-20T>C rs1553277672

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