ClinVar Miner

List of variants in gene NEFL reported as benign for Charcot-Marie-Tooth disease

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)
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Total variants: 3

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HGVS	dbSNP
NM_006158.4(NEFL):c.667C>T (p.Leu223=)	rs60156239
NM_006158.5(NEFL):c.1407G>A (p.Glu469=)	rs543609297
NM_006158.5(NEFL):c.507G>A (p.Glu169=)

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