ClinVar Miner

List of variants reported as pathogenic for Hereditary sensory and autonomic neuropathy type IC by OMIM

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_004863.3(SPTLC2):c.1151C>T (p.Ser384Phe) rs1594986869
NM_004863.3(SPTLC2):c.529A>G (p.Asn177Asp) rs1131691917
NM_004863.3(SPTLC2):c.544G>C (p.Ala182Pro) rs864621998

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.