List of variants in gene NEFH reported as likely benign for amyotrophic lateral sclerosis

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_021076.4(NEFH):c.1740C>T (p.Ser580=)	rs114263951	0.00755
NM_021076.4(NEFH):c.1947_1964dup (p.646_651AKSPEK[3])	rs147489453

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