rs7040561
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7040561(A;A) |
Make rs7040561(A;T) |
Make rs7040561(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 125766699 |
Gene | PBX3 |
is a | snp |
is | mentioned by |
dbSNP | rs7040561 |
dbSNP (classic) | rs7040561 |
ClinGen | rs7040561 |
ebi | rs7040561 |
HLI | rs7040561 |
Exac | rs7040561 |
Gnomad | rs7040561 |
Varsome | rs7040561 |
LitVar | rs7040561 |
Map | rs7040561 |
PheGenI | rs7040561 |
Biobank | rs7040561 |
1000 genomes | rs7040561 |
hgdp | rs7040561 |
ensembl | rs7040561 |
geneview | rs7040561 |
scholar | rs7040561 |
rs7040561 | |
pharmgkb | rs7040561 |
gwascentral | rs7040561 |
openSNP | rs7040561 |
23andMe | rs7040561 |
SNPshot | rs7040561 |
SNPdbe | rs7040561 |
MSV3d | rs7040561 |
GWAS Ctlg | rs7040561 |
GMAF | 0.09688 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 19626039] Lack of replication of celiac disease risk variants reported in a Spanish population using an independent Spanish sample
[PMID 18241860] Combined functional and positional gene information for the identification of susceptibility variants in celiac disease.
[PMID 18471539] No evidence in a large UK collection for celiac disease risk variants reported by a Spanish study.