List of variants in gene combination EVI2A, NF1 reported as benign

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_014210.4(EVI2A):c.156C>T (p.Gly52=)	rs148409995	0.00292
NM_001042492.3(NF1):c.4836-7135A>G	rs149991818	0.00004
NM_014210.4(EVI2A):c.-1C>T	rs1129506

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