ClinVar Miner

List of variants studied for amyotrophic neuralgia

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_001113491.2(SEPTIN9):c.1726A>G (p.Met576Val) rs2627223
NM_001113491.2(SEPTIN9):c.316C>T (p.Arg106Trp) rs80338761
NM_001113491.2(SEPTIN9):c.332C>T (p.Ser111Phe) rs80338762
NM_001113491.2(SEPTIN9):c.721+2405G>A rs2164449
NM_001113491.2(SEPTIN9):c.76+19T>C rs4789439
NM_001113491.2(SEPTIN9):c.77-28563T>C rs7217986
NM_006640.4(SEPTIN9):c.-134G>C rs80338760
SEPT9, 38-KB DUP

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.