rs17035378
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17035378(C;C) |
Make rs17035378(C;T) |
Make rs17035378(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 68371823 |
Gene | LOC101927723, PLEK |
is a | snp |
is | mentioned by |
dbSNP | rs17035378 |
dbSNP (classic) | rs17035378 |
ClinGen | rs17035378 |
ebi | rs17035378 |
HLI | rs17035378 |
Exac | rs17035378 |
Gnomad | rs17035378 |
Varsome | rs17035378 |
LitVar | rs17035378 |
Map | rs17035378 |
PheGenI | rs17035378 |
Biobank | rs17035378 |
1000 genomes | rs17035378 |
hgdp | rs17035378 |
ensembl | rs17035378 |
geneview | rs17035378 |
scholar | rs17035378 |
rs17035378 | |
pharmgkb | rs17035378 |
gwascentral | rs17035378 |
openSNP | rs17035378 |
23andMe | rs17035378 |
SNPshot | rs17035378 |
SNPdbe | rs17035378 |
MSV3d | rs17035378 |
GWAS Ctlg | rs17035378 |
GMAF | 0.4421 |
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 | |
P-val | 8E-9 |
Odds Ratio | 1.14 [1.09-1.19] |