List of variants in gene NPM1 reported as likely benign for hematopoietic and lymphoid cell neoplasm

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_002520.7(NPM1):c.847-5T>C	rs191111314	0.01680
NM_002520.7(NPM1):c.543T>C (p.Phe181=)	rs61755048	0.00991

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