ClinVar Miner

List of variants reported as benign for Amyotrophic lateral sclerosis type 10 by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_007375.3(TARDBP):c.-122G>A rs11121679 0.13475
NM_007375.4(TARDBP):c.*208G>A rs148414479 0.02507
NM_007375.4(TARDBP):c.*2331A>G rs114897688 0.02160
NM_007375.4(TARDBP):c.675A>G (p.Pro225=) rs61741294 0.00675
NM_007375.4(TARDBP):c.*343G>A rs555353123 0.00073
NM_007375.4(TARDBP):c.*1081C>T rs184303021 0.00053
NM_007375.4(TARDBP):c.*2740G>A rs566658679 0.00024
NM_007375.4(TARDBP):c.*73G>C rs185638796 0.00003
NM_007375.4(TARDBP):c.238+9C>T rs376560308 0.00002

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.