List of variants in gene combination EVI2A, NF1 reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.4836-6844T>C	rs144746834	0.00096
NM_014210.4(EVI2A):c.449C>A (p.Thr150Asn)	rs774655791	0.00002
NM_001042492.3(NF1):c.4836-7203TGT[3]	rs773381280
NM_014210.4(EVI2A):c.101G>A (p.Arg34His)	rs532490487

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