List of variants in gene combination LOC130067355, RAC2 reported as benign for hematologic disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002872.5(RAC2):c.448+37A>G	rs9610682	0.41562
NM_002872.5(RAC2):c.448+11C>T	rs530853255
NM_002872.5(RAC2):c.448+25C>G	rs9610683

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