ClinVar Miner

List of variants reported as pathogenic for chronic leukemia by Molecular Genetics Lab, CHRU Brest

Included ClinVar conditions (10):

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_002834.5(PTPN11):c.922A>G (p.Asn308Asp)	rs28933386	0.00001
NM_001042492.3(NF1):c.55G>T (p.Glu19Ter)	rs786203307

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