rs11645366
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11645366(C;C) |
Make rs11645366(C;T) |
Make rs11645366(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 62343249 |
is a | snp |
is | mentioned by |
dbSNP | rs11645366 |
dbSNP (classic) | rs11645366 |
ClinGen | rs11645366 |
ebi | rs11645366 |
HLI | rs11645366 |
Exac | rs11645366 |
Gnomad | rs11645366 |
Varsome | rs11645366 |
LitVar | rs11645366 |
Map | rs11645366 |
PheGenI | rs11645366 |
Biobank | rs11645366 |
1000 genomes | rs11645366 |
hgdp | rs11645366 |
ensembl | rs11645366 |
geneview | rs11645366 |
scholar | rs11645366 |
rs11645366 | |
pharmgkb | rs11645366 |
gwascentral | rs11645366 |
openSNP | rs11645366 |
23andMe | rs11645366 |
SNPshot | rs11645366 |
SNPdbe | rs11645366 |
MSV3d | rs11645366 |
GWAS Ctlg | rs11645366 |
GMAF | 0.1322 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | C |
P-val | 0.000007 |
Odds Ratio | None None |