rs17684824
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17684824(A;A) |
Make rs17684824(A;C) |
Make rs17684824(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 3546358 |
Gene | LOC100130207 |
is a | snp |
is | mentioned by |
dbSNP | rs17684824 |
dbSNP (classic) | rs17684824 |
ClinGen | rs17684824 |
ebi | rs17684824 |
HLI | rs17684824 |
Exac | rs17684824 |
Gnomad | rs17684824 |
Varsome | rs17684824 |
LitVar | rs17684824 |
Map | rs17684824 |
PheGenI | rs17684824 |
Biobank | rs17684824 |
1000 genomes | rs17684824 |
hgdp | rs17684824 |
ensembl | rs17684824 |
geneview | rs17684824 |
scholar | rs17684824 |
rs17684824 | |
pharmgkb | rs17684824 |
gwascentral | rs17684824 |
openSNP | rs17684824 |
23andMe | rs17684824 |
SNPshot | rs17684824 |
SNPdbe | rs17684824 |
MSV3d | rs17684824 |
GWAS Ctlg | rs17684824 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24529757] |
Trait | Amyotrophic lateral sclerosis (sporadic) |
Title | A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. |
Risk Allele | |
P-val | 4E-6 |
Odds Ratio | NR NR |