ClinVar Miner

List of variants studied for amyotrophic lateral sclerosis type 9 by OMIM

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_002937.5(RNASE4):c.-17-5382G>A rs121909544
NM_002937.5(RNASE4):c.-17-5384C>T rs121909543
NM_002937.5(RNASE4):c.-17-5583A>G rs121909541
NM_002937.5(RNASE4):c.-17-5600A>T rs121909540
NM_002937.5(RNASE4):c.-17-5602C>G rs121909539
NM_002937.5(RNASE4):c.-17-5627G>A rs121909538
NM_002937.5(RNASE4):c.-17-5636G>A rs121909542
NM_002937.5(RNASE4):c.-17-5669A>T rs121909536
NM_002937.5(RNASE4):c.-17-5670A>G rs121909537
NM_002937.5(RNASE4):c.-17-5684A>T rs121909535

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.