List of variants in gene SPTLC1 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: 7

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HGVS	dbSNP
NM_006415.4(SPTLC1):c.1136+12A>G	rs76562923
NM_006415.4(SPTLC1):c.1137-23GT[6]	rs147137401
NM_006415.4(SPTLC1):c.1254+10C>T	rs200704785
NM_006415.4(SPTLC1):c.1255-7C>T	rs7863487
NM_006415.4(SPTLC1):c.452G>T (p.Arg151Leu)	rs45461899
NM_006415.4(SPTLC1):c.560+16G>C	rs73512337
NM_006415.4(SPTLC1):c.781-6A>G	rs138268337

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