List of variants in gene RAB3GAP1 reported as uncertain significance for Warburg micro syndrome 1; Martsolf 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_012233.3(RAB3GAP1):c.1226C>T (p.Thr409Ile)	rs149010855	0.00030
NM_012233.3(RAB3GAP1):c.2946A>G (p.Ter982Trp)	rs141436429	0.00021
NM_012233.3(RAB3GAP1):c.2917G>A (p.Ala973Thr)	rs770189875	0.00004
NM_012233.3(RAB3GAP1):c.235C>T (p.Leu79Phe)

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