rs802734
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs802734(C;C) |
Make rs802734(C;T) |
Make rs802734(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 127957653 |
is a | snp |
is | mentioned by |
dbSNP | rs802734 |
dbSNP (classic) | rs802734 |
ClinGen | rs802734 |
ebi | rs802734 |
HLI | rs802734 |
Exac | rs802734 |
Gnomad | rs802734 |
Varsome | rs802734 |
LitVar | rs802734 |
Map | rs802734 |
PheGenI | rs802734 |
Biobank | rs802734 |
1000 genomes | rs802734 |
hgdp | rs802734 |
ensembl | rs802734 |
geneview | rs802734 |
scholar | rs802734 |
rs802734 | |
pharmgkb | rs802734 |
gwascentral | rs802734 |
openSNP | rs802734 |
23andMe | rs802734 |
SNPshot | rs802734 |
SNPdbe | rs802734 |
MSV3d | rs802734 |
GWAS Ctlg | rs802734 |
GMAF | 0.1983 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20190752] |
Trait | Celiac disease |
Title | Multiple common variants for celiac disease influencing immune gene expression |
Risk Allele | G |
P-val | 3E-14 |
Odds Ratio | 1.17 [1.12-1.22] |
GWAS snp | |
---|---|
PMID | [PMID 21833088] |
Trait | |
Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Risk Allele | A |
P-val | 6E-9 |
Odds Ratio | 1.1000 [1.09-1.12] |
[PMID 23820479] THEMIS and PTPRK in celiac intestinal mucosa: coexpression in disease and after in vitro gliadin challenge.