List of variants in gene RAB3GAP2 reported as likely benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_012414.4(RAB3GAP2):c.3495G>A (p.Leu1165=)	rs11547779	0.06867
NM_012414.4(RAB3GAP2):c.3275G>C (p.Ser1092Thr)	rs2289189	0.06844
NM_012414.4(RAB3GAP2):c.2587A>G (p.Thr863Ala)	rs12045447	0.04740
NM_012414.4(RAB3GAP2):c.2088A>G (p.Thr696=)	rs2577126	0.03652
NM_012414.4(RAB3GAP2):c.1779+7G>A	rs111345353	0.00390
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.3991C>A (p.Leu1331Ile)	rs149842844	0.00050
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.2807-15G>A	rs200407685	0.00038
NM_012414.4(RAB3GAP2):c.2667T>G (p.Leu889=)	rs145550355	0.00021
NM_012414.4(RAB3GAP2):c.2304G>A (p.Leu768=)	rs140146408	0.00014
NM_012414.4(RAB3GAP2):c.2212+15A>T	rs375627012	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.1092A>G (p.Gln364=)	rs772862686	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.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.434+14A>G	rs1026065056
NM_012414.4(RAB3GAP2):c.712+12G>T	rs530494745
NM_012414.4(RAB3GAP2):c.713-20T>C	rs1553277672

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