rs12644284
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12644284(A;A) |
Make rs12644284(A;G) |
Make rs12644284(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 153232848 |
Gene | TRIM2 |
is a | snp |
is | mentioned by |
dbSNP | rs12644284 |
dbSNP (classic) | rs12644284 |
ClinGen | rs12644284 |
ebi | rs12644284 |
HLI | rs12644284 |
Exac | rs12644284 |
Gnomad | rs12644284 |
Varsome | rs12644284 |
LitVar | rs12644284 |
Map | rs12644284 |
PheGenI | rs12644284 |
Biobank | rs12644284 |
1000 genomes | rs12644284 |
hgdp | rs12644284 |
ensembl | rs12644284 |
geneview | rs12644284 |
scholar | rs12644284 |
rs12644284 | |
pharmgkb | rs12644284 |
gwascentral | rs12644284 |
openSNP | rs12644284 |
23andMe | rs12644284 |
SNPshot | rs12644284 |
SNPdbe | rs12644284 |
MSV3d | rs12644284 |
GWAS Ctlg | rs12644284 |
GMAF | 0.1515 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21654844] |
Trait | |
Title | Genome-wide association study of severity in multiple sclerosis. |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | 2.0400 [NR] |