rs7672826
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7672826(A;A) |
Make rs7672826(A;G) |
Make rs7672826(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 181478542 |
Gene | TENM3 |
is a | snp |
is | mentioned by |
dbSNP | rs7672826 |
dbSNP (classic) | rs7672826 |
ClinGen | rs7672826 |
ebi | rs7672826 |
HLI | rs7672826 |
Exac | rs7672826 |
Gnomad | rs7672826 |
Varsome | rs7672826 |
LitVar | rs7672826 |
Map | rs7672826 |
PheGenI | rs7672826 |
Biobank | rs7672826 |
1000 genomes | rs7672826 |
hgdp | rs7672826 |
ensembl | rs7672826 |
geneview | rs7672826 |
scholar | rs7672826 |
rs7672826 | |
pharmgkb | rs7672826 |
gwascentral | rs7672826 |
openSNP | rs7672826 |
23andMe | rs7672826 |
SNPshot | rs7672826 |
SNPdbe | rs7672826 |
MSV3d | rs7672826 |
GWAS Ctlg | rs7672826 |
GMAF | 0.3577 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19010793] |
Trait | Multiple sclerosis |
Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | 1.37 [NR] |
[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.