ClinVar Miner

List of variants reported as benign for neoplasm of immature B and T cells by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (13):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_002485.5(NBN):c.37+11A>G	rs115032431	0.00540
NM_002485.5(NBN):c.381T>C (p.Ala127=)	rs61754795	0.00266

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