rs16902328
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16902328(G;G) |
Make rs16902328(G;T) |
Make rs16902328(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 127701628 |
Gene | CASC11 |
is a | snp |
is | mentioned by |
dbSNP | rs16902328 |
dbSNP (classic) | rs16902328 |
ClinGen | rs16902328 |
ebi | rs16902328 |
HLI | rs16902328 |
Exac | rs16902328 |
Gnomad | rs16902328 |
Varsome | rs16902328 |
LitVar | rs16902328 |
Map | rs16902328 |
PheGenI | rs16902328 |
Biobank | rs16902328 |
1000 genomes | rs16902328 |
hgdp | rs16902328 |
ensembl | rs16902328 |
geneview | rs16902328 |
scholar | rs16902328 |
rs16902328 | |
pharmgkb | rs16902328 |
gwascentral | rs16902328 |
openSNP | rs16902328 |
23andMe | rs16902328 |
SNPshot | rs16902328 |
SNPdbe | rs16902328 |
MSV3d | rs16902328 |
GWAS Ctlg | rs16902328 |
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 | 3E-6 |
Odds Ratio | NR NR |