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

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
NC_000017.10:g.(?_29645324)_(29653290_?)dup
NM_001042492.3(NF1):c.5030TCTATA[1] (p.Ile1679_Tyr1680del)	rs1135402868
NM_001042492.3(NF1):c.5268+5G>T	rs864622551

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