List of variants in gene RAB3GAP2 reported as benign for Warburg micro syndrome 2

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_012414.4(RAB3GAP2):c.*404T>C	rs1059140	0.06883
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.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.*1504G>T	rs41303053	0.03924
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.*1130A>G	rs548918189	0.00800
NM_012414.4(RAB3GAP2):c.1779+7G>A	rs111345353	0.00390
NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=)	rs73098539	0.00338
NM_012414.4(RAB3GAP2):c.*925C>T	rs185747953	0.00318
NM_012414.4(RAB3GAP2):c.1709A>G (p.Asn570Ser)	rs143286302	0.00006
NM_012414.4(RAB3GAP2):c.*2043G>A	rs367962640	0.00003
NM_012414.4(RAB3GAP2):c.2522C>T (p.Ala841Val)	rs764713903	0.00003
NM_012414.4(RAB3GAP2):c.2008C>G (p.Leu670Val)	rs201613456	0.00002

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