ClinVar Miner

List of variants reported as benign for Amyotrophic Lateral Sclerosis, Dominant by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006610.4(MASP2):c.*225T>C rs1033638 0.69325
NM_006610.4(MASP2):c.1479C>T (p.Ser493=) rs1782455 0.67756
NM_004629.2(FANCG):c.1636+7A>G rs587118 0.35683
NM_015046.7(SETX):c.5781+12dup rs3831154 0.24271
NM_004738.5(VAPB):c.*3428CATGTGTG[2] rs3069390
NM_007126.5(VCP):c.1082-18_1082-8dup rs11272867
NM_007375.4(TARDBP):c.*2294_*2295insGTTTT rs3059695

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.