rs12727642
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12727642(A;A) |
Make rs12727642(A;C) |
Make rs12727642(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 7986612 |
Gene | PARK7 |
is a | snp |
is | mentioned by |
dbSNP | rs12727642 |
dbSNP (classic) | rs12727642 |
ClinGen | rs12727642 |
ebi | rs12727642 |
HLI | rs12727642 |
Exac | rs12727642 |
Gnomad | rs12727642 |
Varsome | rs12727642 |
LitVar | rs12727642 |
Map | rs12727642 |
PheGenI | rs12727642 |
Biobank | rs12727642 |
1000 genomes | rs12727642 |
hgdp | rs12727642 |
ensembl | rs12727642 |
geneview | rs12727642 |
scholar | rs12727642 |
rs12727642 | |
pharmgkb | rs12727642 |
gwascentral | rs12727642 |
openSNP | rs12727642 |
23andMe | rs12727642 |
SNPshot | rs12727642 |
SNPdbe | rs12727642 |
MSV3d | rs12727642 |
GWAS Ctlg | rs12727642 |
GMAF | 0.09734 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20190752] |
Trait | Celiac disease |
Title | Multiple common variants for celiac disease influencing immune gene expression |
Risk Allele | A |
P-val | 9E-8 |
Odds Ratio | 1.14 [1.09-1.20] |
[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression