List of variants in gene TTR reported as likely 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)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP
NM_000371.3(TTR):c.336+19G>A	rs75517067
NM_000371.3(TTR):c.384C>T (p.Ala128=)	rs143906738
NM_000371.3(TTR):c.70-19G>A	rs548935944
NM_000371.4(TTR):c.14G>A (p.Arg5His)	rs138657343
NM_000371.4(TTR):c.201-3T>C
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074
NM_000371.4(TTR):c.337-13T>C	rs762691667
NM_000371.4(TTR):c.416C>T (p.Thr139Met)	rs28933981
NM_000371.4(TTR):c.417G>A (p.Thr139=)	rs2276382
NM_000371.4(TTR):c.75C>T (p.Thr25=)

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