List of variants in gene RAB3GAP2 reported by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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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.39C>T (p.Asp13=)	rs145667920	0.00149
NM_012414.4(RAB3GAP2):c.3842A>G (p.Tyr1281Cys)	rs34081806	0.00094
NM_012414.4(RAB3GAP2):c.3991C>A (p.Leu1331Ile)	rs149842844	0.00050
NM_012414.4(RAB3GAP2):c.3702C>T (p.Val1234=)	rs137897304	0.00041
NM_012414.4(RAB3GAP2):c.1984C>T (p.Pro662Ser)	rs779101759	0.00001
NM_012414.4(RAB3GAP2):c.1836C>A (p.Ile612=)	rs794727209
NM_012414.4(RAB3GAP2):c.3868-10C>G	rs1310779201

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