ClinVar Miner

List of variants reported as uncertain significance for autosomal dominant slowed nerve conduction velocity by Baylor Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014629.4(ARHGEF10):c.2063G>A (p.Ser688Asn) rs143290224 0.00051
NM_014629.4(ARHGEF10):c.121G>T (p.Glu41Ter) rs764859351
NM_014629.4(ARHGEF10):c.1343A>G (p.Glu448Gly) rs1809808538
NM_014629.4(ARHGEF10):c.2134G>T (p.Ala712Ser) rs1057523214

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.