rs12188164
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12188164(A;A) |
Make rs12188164(A;C) |
Make rs12188164(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 428121 |
Gene | AHRR |
is a | snp |
is | mentioned by |
dbSNP | rs12188164 |
dbSNP (classic) | rs12188164 |
ClinGen | rs12188164 |
ebi | rs12188164 |
HLI | rs12188164 |
Exac | rs12188164 |
Gnomad | rs12188164 |
Varsome | rs12188164 |
LitVar | rs12188164 |
Map | rs12188164 |
PheGenI | rs12188164 |
Biobank | rs12188164 |
1000 genomes | rs12188164 |
hgdp | rs12188164 |
ensembl | rs12188164 |
geneview | rs12188164 |
scholar | rs12188164 |
rs12188164 | |
pharmgkb | rs12188164 |
gwascentral | rs12188164 |
openSNP | rs12188164 |
23andMe | rs12188164 |
SNPshot | rs12188164 |
SNPdbe | rs12188164 |
MSV3d | rs12188164 |
GWAS Ctlg | rs12188164 |
GMAF | 0.1878 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21602797] |
Trait | |
Title | Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. |
Risk Allele | A |
P-val | 0.000004 |
Odds Ratio | None None |