List of variants in gene RAB3GAP2 reported as uncertain significance for amenorrhea

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012414.4(RAB3GAP2):c.1258C>T (p.Arg420Cys)	rs188522997	0.00033
NM_012414.4(RAB3GAP2):c.1580C>T (p.Pro527Leu)	rs149563712	0.00019
NM_012414.4(RAB3GAP2):c.3616G>T (p.Asp1206Tyr)	rs139407102	0.00016

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