Variants in gene RAB3GAP2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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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.3867+13C>T	rs200579008	0.00087
NM_012414.4(RAB3GAP2):c.1215C>T (p.Phe405=)	rs762485949	0.00009
NM_012414.4(RAB3GAP2):c.1709A>G (p.Asn570Ser)	rs143286302	0.00006
NM_012414.4(RAB3GAP2):c.812-7_812-6del	rs35396665

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