rs905080
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs905080(C;C) |
Make rs905080(C;G) |
Make rs905080(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 43315125 |
is a | snp |
is | mentioned by |
dbSNP | rs905080 |
dbSNP (classic) | rs905080 |
ClinGen | rs905080 |
ebi | rs905080 |
HLI | rs905080 |
Exac | rs905080 |
Gnomad | rs905080 |
Varsome | rs905080 |
LitVar | rs905080 |
Map | rs905080 |
PheGenI | rs905080 |
Biobank | rs905080 |
1000 genomes | rs905080 |
hgdp | rs905080 |
ensembl | rs905080 |
geneview | rs905080 |
scholar | rs905080 |
rs905080 | |
pharmgkb | rs905080 |
gwascentral | rs905080 |
openSNP | rs905080 |
23andMe | rs905080 |
SNPshot | rs905080 |
SNPdbe | rs905080 |
MSV3d | rs905080 |
GWAS Ctlg | rs905080 |
GMAF | 0.1671 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]