List of variants in gene RAB3GAP2 reported as uncertain significance 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_012414.4(RAB3GAP2):c.4060A>G (p.Ile1354Val)	rs59190330	0.00174
NM_012414.4(RAB3GAP2):c.2290C>T (p.Leu764Phe)	rs139337049	0.00097
NM_012414.4(RAB3GAP2):c.3525C>T (p.Thr1175=)	rs145701892	0.00056
NM_012414.4(RAB3GAP2):c.1406C>T (p.Ala469Val)	rs151225064	0.00008
NM_012414.4(RAB3GAP2):c.1657G>A (p.Asp553Asn)	rs199952665	0.00006
NM_012414.4(RAB3GAP2):c.3944C>T (p.Ala1315Val)	rs202192080	0.00004
NM_012414.4(RAB3GAP2):c.2522C>T (p.Ala841Val)	rs764713903	0.00003
NM_012414.4(RAB3GAP2):c.2008C>G (p.Leu670Val)	rs201613456	0.00002
NM_012414.4(RAB3GAP2):c.655A>G (p.Ile219Val)	rs1345506404	0.00002
NM_012414.4(RAB3GAP2):c.1205C>G (p.Thr402Arg)	rs763764406	0.00001
NM_012414.4(RAB3GAP2):c.3028G>A (p.Asp1010Asn)	rs763047721	0.00001
NM_012414.4(RAB3GAP2):c.379G>A (p.Glu127Lys)	rs747224775	0.00001
NM_012414.4(RAB3GAP2):c.3818A>G (p.His1273Arg)	rs370057302	0.00001
NM_012414.4(RAB3GAP2):c.504C>T (p.Tyr168=)	rs778754576	0.00001
NM_012414.4(RAB3GAP2):c.1030A>G (p.Asn344Asp)	rs1174986383
NM_012414.4(RAB3GAP2):c.1631+8G>T	rs1553276397
NM_012414.4(RAB3GAP2):c.2207C>T (p.Ala736Val)
NM_012414.4(RAB3GAP2):c.2269C>T (p.His757Tyr)	rs1553275637
NM_012414.4(RAB3GAP2):c.2648C>T (p.Thr883Ile)	rs797045906
NM_012414.4(RAB3GAP2):c.278G>C (p.Arg93Pro)	rs371630366
NM_012414.4(RAB3GAP2):c.3965AAG[1] (p.Glu1323del)	rs371310481
NM_012414.4(RAB3GAP2):c.4025T>C (p.Met1342Thr)	rs1553272940

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