rs16975050
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
Make rs16975050(G;G) |
Make rs16975050(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 41607206 |
is a | snp |
is | mentioned by |
dbSNP | rs16975050 |
dbSNP (classic) | rs16975050 |
ClinGen | rs16975050 |
ebi | rs16975050 |
HLI | rs16975050 |
Exac | rs16975050 |
Gnomad | rs16975050 |
Varsome | rs16975050 |
LitVar | rs16975050 |
Map | rs16975050 |
PheGenI | rs16975050 |
Biobank | rs16975050 |
1000 genomes | rs16975050 |
hgdp | rs16975050 |
ensembl | rs16975050 |
geneview | rs16975050 |
scholar | rs16975050 |
rs16975050 | |
pharmgkb | rs16975050 |
gwascentral | rs16975050 |
openSNP | rs16975050 |
23andMe | rs16975050 |
SNPshot | rs16975050 |
SNPdbe | rs16975050 |
MSV3d | rs16975050 |
GWAS Ctlg | rs16975050 |
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 | 5E-7 |
Odds Ratio | NR NR |