rs12704645
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12704645(C;C) |
Make rs12704645(C;T) |
Make rs12704645(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 92993336 |
is a | snp |
is | mentioned by |
dbSNP | rs12704645 |
dbSNP (classic) | rs12704645 |
ClinGen | rs12704645 |
ebi | rs12704645 |
HLI | rs12704645 |
Exac | rs12704645 |
Gnomad | rs12704645 |
Varsome | rs12704645 |
LitVar | rs12704645 |
Map | rs12704645 |
PheGenI | rs12704645 |
Biobank | rs12704645 |
1000 genomes | rs12704645 |
hgdp | rs12704645 |
ensembl | rs12704645 |
geneview | rs12704645 |
scholar | rs12704645 |
rs12704645 | |
pharmgkb | rs12704645 |
gwascentral | rs12704645 |
openSNP | rs12704645 |
23andMe | rs12704645 |
SNPshot | rs12704645 |
SNPdbe | rs12704645 |
MSV3d | rs12704645 |
GWAS Ctlg | rs12704645 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24939585] |
Trait | Age-related hearing impairment |
Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
Risk Allele | |
P-val | 8E-6 |
Odds Ratio | .06 [NR] unit increase |