List of variants in gene HINT1 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: 4

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HGVS	dbSNP
NM_005340.7(HINT1):c.182C>T (p.Ser61Phe)	rs1580684630
NM_005340.7(HINT1):c.316C>T (p.Gln106Ter)	rs1028404937
NM_005340.7(HINT1):c.341A>G (p.His114Arg)	rs1580682427
NM_005340.7(HINT1):c.368G>A (p.Trp123Ter)	rs1580682390

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