rs11209454
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11209454(A;A) |
Make rs11209454(A;G) |
Make rs11209454(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 69424008 |
is a | snp |
is | mentioned by |
dbSNP | rs11209454 |
dbSNP (classic) | rs11209454 |
ClinGen | rs11209454 |
ebi | rs11209454 |
HLI | rs11209454 |
Exac | rs11209454 |
Gnomad | rs11209454 |
Varsome | rs11209454 |
LitVar | rs11209454 |
Map | rs11209454 |
PheGenI | rs11209454 |
Biobank | rs11209454 |
1000 genomes | rs11209454 |
hgdp | rs11209454 |
ensembl | rs11209454 |
geneview | rs11209454 |
scholar | rs11209454 |
rs11209454 | |
pharmgkb | rs11209454 |
gwascentral | rs11209454 |
openSNP | rs11209454 |
23andMe | rs11209454 |
SNPshot | rs11209454 |
SNPdbe | rs11209454 |
MSV3d | rs11209454 |
GWAS Ctlg | rs11209454 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24939585] |
Trait | Age-related hearing impairment (interaction) |
Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
Risk Allele | |
P-val | 5E-9 |
Odds Ratio | NR NR |