List of variants in gene combination LOC130067355, RAC2 reported as likely benign for immune system disorder

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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_002872.5(RAC2):c.448+12G>A	rs373971208	0.00008
NM_002872.5(RAC2):c.420G>A (p.Pro140=)	rs539660525	0.00004
NM_002872.5(RAC2):c.426C>T (p.Gly142=)
NM_002872.5(RAC2):c.427C>T (p.Leu143=)
NM_002872.5(RAC2):c.432A>C (p.Ala144=)
NM_002872.5(RAC2):c.448+18A>C
NM_002872.5(RAC2):c.448+7G>T

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