rs3749146
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3749146(C;C) |
Make rs3749146(C;T) |
Make rs3749146(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 48597362 |
Gene | STON1, STON1-GTF2A1L |
is a | snp |
is | mentioned by |
dbSNP | rs3749146 |
dbSNP (classic) | rs3749146 |
ClinGen | rs3749146 |
ebi | rs3749146 |
HLI | rs3749146 |
Exac | rs3749146 |
Gnomad | rs3749146 |
Varsome | rs3749146 |
LitVar | rs3749146 |
Map | rs3749146 |
PheGenI | rs3749146 |
Biobank | rs3749146 |
1000 genomes | rs3749146 |
hgdp | rs3749146 |
ensembl | rs3749146 |
geneview | rs3749146 |
scholar | rs3749146 |
rs3749146 | |
pharmgkb | rs3749146 |
gwascentral | rs3749146 |
openSNP | rs3749146 |
23andMe | rs3749146 |
SNPshot | rs3749146 |
SNPdbe | rs3749146 |
MSV3d | rs3749146 |
GWAS Ctlg | rs3749146 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 3E-6 |
Odds Ratio | NR NR |