rs4916321
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs4916321(G;T) |
Make rs4916321(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 173315060 |
Gene | LOC100506023, TNFSF4 |
is a | snp |
is | mentioned by |
dbSNP | rs4916321 |
dbSNP (classic) | rs4916321 |
ClinGen | rs4916321 |
ebi | rs4916321 |
HLI | rs4916321 |
Exac | rs4916321 |
Gnomad | rs4916321 |
Varsome | rs4916321 |
LitVar | rs4916321 |
Map | rs4916321 |
PheGenI | rs4916321 |
Biobank | rs4916321 |
1000 genomes | rs4916321 |
hgdp | rs4916321 |
ensembl | rs4916321 |
geneview | rs4916321 |
scholar | rs4916321 |
rs4916321 | |
pharmgkb | rs4916321 |
gwascentral | rs4916321 |
openSNP | rs4916321 |
23andMe | rs4916321 |
SNPshot | rs4916321 |
SNPdbe | rs4916321 |
MSV3d | rs4916321 |
GWAS Ctlg | rs4916321 |
GMAF | 0.06336 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23412934] |
Trait | Multiple sclerosis |
Title | A genome-wide association study of brain lesion distribution in multiple sclerosis. |
Risk Allele | |
P-val | 7E-6 |
Odds Ratio | NR NR |