List of variants in gene RAC1 reported as uncertain significance for multiple congenital anomalies/dysmorphic syndrome-intellectual disability

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006908.5(RAC1):c.170A>C (p.Asp57Ala)
NM_006908.5(RAC1):c.176C>G (p.Ala59Gly)
NM_006908.5(RAC1):c.280C>T (p.Arg94Cys)
NM_006908.5(RAC1):c.372C>G (p.Asp124Glu)	rs1227283234
NM_006908.5(RAC1):c.409A>G (p.Ile137Val)	rs770760146
NM_006908.5(RAC1):c.478C>G (p.Leu160Val)
NM_006908.5(RAC1):c.506T>G (p.Phe169Cys)	rs1176320808

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