rs1958589
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1958589(C;C) |
Make rs1958589(C;T) |
Make rs1958589(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 14 |
Position | 34375170 |
is a | snp |
is | mentioned by |
dbSNP | rs1958589 |
dbSNP (classic) | rs1958589 |
ClinGen | rs1958589 |
ebi | rs1958589 |
HLI | rs1958589 |
Exac | rs1958589 |
Gnomad | rs1958589 |
Varsome | rs1958589 |
LitVar | rs1958589 |
Map | rs1958589 |
PheGenI | rs1958589 |
Biobank | rs1958589 |
1000 genomes | rs1958589 |
hgdp | rs1958589 |
ensembl | rs1958589 |
geneview | rs1958589 |
scholar | rs1958589 |
rs1958589 | |
pharmgkb | rs1958589 |
gwascentral | rs1958589 |
openSNP | rs1958589 |
23andMe | rs1958589 |
SNPshot | rs1958589 |
SNPdbe | rs1958589 |
MSV3d | rs1958589 |
GWAS Ctlg | rs1958589 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23936387] |
Trait | Celiac disease |
Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
Risk Allele | C |
P-val | 4E-6 |
Odds Ratio | NR NR |