ClinVar Miner

List of variants in gene RAB3GAP2 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_012414.4(RAB3GAP2):c.3261+176G>A rs2789792 0.48385
NM_012414.4(RAB3GAP2):c.3226-113C>T rs2808026 0.48380
NM_012414.4(RAB3GAP2):c.116-86T>C rs10863538 0.46438
NM_012414.4(RAB3GAP2):c.613-155C>G rs4142940 0.46320
NM_012414.4(RAB3GAP2):c.612+281G>C rs4511114 0.46117
NM_012414.4(RAB3GAP2):c.3225+110T>C rs2164790 0.27982
NM_012414.4(RAB3GAP2):c.713-237T>A rs7541290 0.24664
NM_012414.4(RAB3GAP2):c.305-278G>A rs59681037 0.16160
NM_012414.4(RAB3GAP2):c.304+330A>G rs57557703 0.16149
NM_012414.4(RAB3GAP2):c.2417-181T>G rs73098558 0.12787
NM_012414.4(RAB3GAP2):c.181-284A>G rs112445597 0.12191
NM_012414.4(RAB3GAP2):c.115+247G>A rs73095636 0.08650
NM_012414.4(RAB3GAP2):c.811+199T>A rs112529023 0.08462
NM_012414.4(RAB3GAP2):c.613-208C>A rs56357312 0.08425
NM_012414.4(RAB3GAP2):c.1780-154C>A rs17622257 0.08106
NM_012414.4(RAB3GAP2):c.304+115C>T rs147804604 0.07969
NM_012414.4(RAB3GAP2):c.1271-224G>A rs79314046 0.07051
NM_012414.4(RAB3GAP2):c.3495G>A (p.Leu1165=) rs11547779 0.06867
NM_012414.4(RAB3GAP2):c.2416+101T>C rs41303055 0.06850
NM_012414.4(RAB3GAP2):c.3262-80G>C rs3767655 0.06848
NM_012414.4(RAB3GAP2):c.3275G>C (p.Ser1092Thr) rs2289189 0.06844
NM_012414.4(RAB3GAP2):c.1131-225G>A rs79287176 0.06779
NM_012414.4(RAB3GAP2):c.1270+85A>T rs78010602 0.06774
NM_012414.4(RAB3GAP2):c.115+77G>A rs2292418 0.06638
NM_012414.4(RAB3GAP2):c.1998+77A>G rs73098569 0.05603
NM_012414.4(RAB3GAP2):c.1041-18A>C rs73098579 0.04963
NM_012414.4(RAB3GAP2):c.3868-31C>G rs12032738 0.04866
NM_012414.4(RAB3GAP2):c.2587A>G (p.Thr863Ala) rs12045447 0.04740
NM_012414.4(RAB3GAP2):c.1779+263G>A rs61830433 0.04739
NM_012414.4(RAB3GAP2):c.304+116C>T rs149818106 0.04682
NM_012414.4(RAB3GAP2):c.2416+119G>A rs7527410 0.04665
NM_012414.4(RAB3GAP2):c.4026+59G>C rs2789790 0.04605
NM_012414.4(RAB3GAP2):c.712+283G>C rs75708871 0.04338
NM_012414.4(RAB3GAP2):c.713-12T>C rs76473498 0.03857
NM_012414.4(RAB3GAP2):c.2088A>G (p.Thr696=) rs2577126 0.03652
NM_012414.4(RAB3GAP2):c.2578-170C>T rs77315325 0.03331
NM_012414.4(RAB3GAP2):c.3155-115A>G rs74139288 0.02679
NM_012414.4(RAB3GAP2):c.811+242C>T rs138654906 0.01676
NM_012414.4(RAB3GAP2):c.961-14G>T rs148886986 0.00475
NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=) rs73098539 0.00338
NM_012414.4(RAB3GAP2):c.3867+13C>T rs200579008 0.00087
NM_012414.4(RAB3GAP2):c.1215C>T (p.Phe405=) rs762485949 0.00009
NM_012414.4(RAB3GAP2):c.1709A>G (p.Asn570Ser) rs143286302 0.00006
NM_012414.4(RAB3GAP2):c.115+294dup rs150613135
NM_012414.4(RAB3GAP2):c.1779+186_1779+187del rs35162828
NM_012414.4(RAB3GAP2):c.1779+187del rs35162828
NM_012414.4(RAB3GAP2):c.1780-264A>G rs17007152
NM_012414.4(RAB3GAP2):c.180+87A>G rs12086760
NM_012414.4(RAB3GAP2):c.2310+165del rs11343960
NM_012414.4(RAB3GAP2):c.2310+198dup rs375756461
NM_012414.4(RAB3GAP2):c.304+112_304+113insTCT rs550502152
NM_012414.4(RAB3GAP2):c.304+121C>T rs138212227
NM_012414.4(RAB3GAP2):c.3154+241dup rs35024056
NM_012414.4(RAB3GAP2):c.3154+259del rs35024056
NM_012414.4(RAB3GAP2):c.3154+278dup rs71169436
NM_012414.4(RAB3GAP2):c.3226-77dup rs11435010
NM_012414.4(RAB3GAP2):c.3262-101A>C rs3767654
NM_012414.4(RAB3GAP2):c.3556-46del rs140309039
NM_012414.4(RAB3GAP2):c.613-14del rs572027376
NM_012414.4(RAB3GAP2):c.811+158A>G rs149591659
NM_012414.4(RAB3GAP2):c.812-6del rs35396665

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