List of variants in gene RAB3GAP1 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_012233.3(RAB3GAP1):c.2265T>C (p.Phe755=)	rs17261772	0.53257
NM_012233.3(RAB3GAP1):c.1793A>G (p.Asn598Ser)	rs10445686	0.14088
NM_012233.3(RAB3GAP1):c.1992G>A (p.Ser664=)	rs7595725	0.02952
NM_012233.3(RAB3GAP1):c.1041A>G (p.Arg347=)	rs77972211	0.01269
NM_012233.3(RAB3GAP1):c.1325A>G (p.Tyr442Cys)	rs114901298	0.01077
NM_012233.3(RAB3GAP1):c.357A>G (p.Val119=)	rs73959261	0.01043
NM_012233.2(RAB3GAP1):c.-53C>G	rs78560065	0.00503
NM_012233.3(RAB3GAP1):c.1006C>T (p.Arg336Cys)	rs150478342	0.00415
NM_012233.3(RAB3GAP1):c.2490+19C>T	rs370595325	0.00113
NM_012233.3(RAB3GAP1):c.2904T>C (p.Phe968=)	rs146045827	0.00092
NM_012233.3(RAB3GAP1):c.411C>T (p.Asp137=)	rs140929274	0.00045
NM_012233.3(RAB3GAP1):c.1719A>G (p.Lys573=)	rs201394875	0.00024
NM_012233.3(RAB3GAP1):c.1326+15A>C	rs185076543	0.00018
NM_012233.3(RAB3GAP1):c.482+18A>G	rs535165082	0.00006
NM_012233.3(RAB3GAP1):c.1499+20A>G	rs201303667	0.00005
NM_012233.3(RAB3GAP1):c.2394C>T (p.Leu798=)	rs550794953	0.00004
NM_012233.3(RAB3GAP1):c.1923+13A>C	rs778152367	0.00003
NM_012233.3(RAB3GAP1):c.2798C>T (p.Pro933Leu)	rs770933323	0.00003
NM_012233.3(RAB3GAP1):c.267G>A (p.Lys89=)	rs757292994	0.00002
NM_012233.3(RAB3GAP1):c.2138T>C (p.Ile713Thr)	rs759109888	0.00001
NM_012233.3(RAB3GAP1):c.2491-10del	rs778684194	0.00001
NM_012233.3(RAB3GAP1):c.2524C>T (p.Leu842Phe)	rs371275629	0.00001
NM_012233.3(RAB3GAP1):c.1697A>C (p.Lys566Thr)	rs1553447342
NM_012233.3(RAB3GAP1):c.18+4A>G	rs550325115
NM_012233.3(RAB3GAP1):c.741A>G (p.Gln247=)	rs1296336356
NM_012233.3(RAB3GAP1):c.831-14T>G	rs1553446155

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