ClinVar Miner

List of variants reported as benign for FTDALS2

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_213720.2(CHCHD10):c.136G>T (p.Ala46Ser) rs200831077
NM_213720.2(CHCHD10):c.234G>A (p.Ser78=) rs111527940
NM_213720.2(CHCHD10):c.286C>A (p.Pro96Thr) rs111677724
NM_213720.2(CHCHD10):c.330G>A (p.Leu110=) rs138183274
NM_213720.2(CHCHD10):c.41+7G>A rs141526972
NM_213720.2(CHCHD10):c.42-7C>G rs567239313

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.