rs758944
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs758944(G;G) |
Make rs758944(G;T) |
Make rs758944(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 76323980 |
is a | snp |
is | mentioned by |
dbSNP | rs758944 |
dbSNP (classic) | rs758944 |
ClinGen | rs758944 |
ebi | rs758944 |
HLI | rs758944 |
Exac | rs758944 |
Gnomad | rs758944 |
Varsome | rs758944 |
LitVar | rs758944 |
Map | rs758944 |
PheGenI | rs758944 |
Biobank | rs758944 |
1000 genomes | rs758944 |
hgdp | rs758944 |
ensembl | rs758944 |
geneview | rs758944 |
scholar | rs758944 |
rs758944 | |
pharmgkb | rs758944 |
gwascentral | rs758944 |
openSNP | rs758944 |
23andMe | rs758944 |
SNPshot | rs758944 |
SNPdbe | rs758944 |
MSV3d | rs758944 |
GWAS Ctlg | rs758944 |
GMAF | 0.3402 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21654844] |
Trait | |
Title | Genome-wide association study of severity in multiple sclerosis. |
Risk Allele | T |
P-val | 0.000008 |
Odds Ratio | 0.4800 [NR] unit increase |