List of variants in gene RAC1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006908.5(RAC1):c.495C>G (p.Leu165=)	rs61753123	0.00215
NM_006908.5(RAC1):c.107+1127A>T
NM_006908.5(RAC1):c.107+1172C>G
NM_006908.5(RAC1):c.107+1183T>C
NM_006908.5(RAC1):c.226-1465G>C	rs1783314244
NM_006908.5(RAC1):c.420G>A (p.Pro140=)
NM_006908.5(RAC1):c.516G>A (p.Ala172=)
NM_006908.5(RAC1):c.81A>G (p.Ala27=)	rs1357653249

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