rs1929412
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1929412(G;G) |
Make rs1929412(G;T) |
Make rs1929412(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 11951222 |
is a | snp |
is | mentioned by |
dbSNP | rs1929412 |
dbSNP (classic) | rs1929412 |
ClinGen | rs1929412 |
ebi | rs1929412 |
HLI | rs1929412 |
Exac | rs1929412 |
Gnomad | rs1929412 |
Varsome | rs1929412 |
LitVar | rs1929412 |
Map | rs1929412 |
PheGenI | rs1929412 |
Biobank | rs1929412 |
1000 genomes | rs1929412 |
hgdp | rs1929412 |
ensembl | rs1929412 |
geneview | rs1929412 |
scholar | rs1929412 |
rs1929412 | |
pharmgkb | rs1929412 |
gwascentral | rs1929412 |
openSNP | rs1929412 |
23andMe | rs1929412 |
SNPshot | rs1929412 |
SNPdbe | rs1929412 |
MSV3d | rs1929412 |
GWAS Ctlg | rs1929412 |
Max Magnitude | 0 |
? | (G;G) (G;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 | 8E-6 |
Odds Ratio | NR NR |