ClinVar Miner

List of variants in gene NF1 reported as likely pathogenic for B-cell neoplasm

Included ClinVar conditions (16):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.5476C>A (p.His1826Asn)	rs1135402871
NM_001042492.3(NF1):c.6921+3A>G	rs1085307885

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