rs1077667
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1077667(A;A) |
Make rs1077667(A;G) |
Make rs1077667(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 6668961 |
Gene | TNFSF14 |
is a | snp |
is | mentioned by |
dbSNP | rs1077667 |
dbSNP (classic) | rs1077667 |
ClinGen | rs1077667 |
ebi | rs1077667 |
HLI | rs1077667 |
Exac | rs1077667 |
Gnomad | rs1077667 |
Varsome | rs1077667 |
LitVar | rs1077667 |
Map | rs1077667 |
PheGenI | rs1077667 |
Biobank | rs1077667 |
1000 genomes | rs1077667 |
hgdp | rs1077667 |
ensembl | rs1077667 |
geneview | rs1077667 |
scholar | rs1077667 |
rs1077667 | |
pharmgkb | rs1077667 |
gwascentral | rs1077667 |
openSNP | rs1077667 |
23andMe | rs1077667 |
SNPshot | rs1077667 |
SNPdbe | rs1077667 |
MSV3d | rs1077667 |
GWAS Ctlg | rs1077667 |
GMAF | 0.2351 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
23andMe blog multiple sclerosis rs1077667 TNFSF14 T 0.88
GWAS snp | |
---|---|
PMID | [PMID 21833088] |
Trait | |
Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Risk Allele | G |
P-val | 9E-14 |
Odds Ratio | 1.1600 [1.14-1.18] |
[PMID 23037546] Serum levels of LIGHT in MS