List of variants in gene NGF reported as uncertain significance 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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP
NM_002506.2(NGF):c.560G>A (p.Ser187Asn)	rs1571069395
NM_002506.2(NGF):c.680C>A (p.Thr227Lys)	rs1326012011
NM_002506.2(NGF):c.681_682del (p.Ala228fs)	rs1571069258

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