List of variants in gene TFG 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)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP
NM_006070.6(TFG):c.1090A>C (p.Thr364Pro)	rs6772054
NM_006070.6(TFG):c.258G>T (p.Leu86=)	rs150620449
NM_006070.6(TFG):c.415+7C>G	rs149927288
NM_006070.6(TFG):c.416-9T>C	rs115896544
NM_006070.6(TFG):c.552G>A (p.Ala184=)	rs35648279
NM_006070.6(TFG):c.594T>G (p.Ala198=)	rs12562
NM_006070.6(TFG):c.663C>A (p.Gly221=)	rs140669729
NM_006070.6(TFG):c.722-8G>T	rs41272979
NM_006070.6(TFG):c.945G>A (p.Pro315=)	rs61736338

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