rs9351104
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9351104(C;C) |
Make rs9351104(C;T) |
Make rs9351104(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 86638087 |
is a | snp |
is | mentioned by |
dbSNP | rs9351104 |
dbSNP (classic) | rs9351104 |
ClinGen | rs9351104 |
ebi | rs9351104 |
HLI | rs9351104 |
Exac | rs9351104 |
Gnomad | rs9351104 |
Varsome | rs9351104 |
LitVar | rs9351104 |
Map | rs9351104 |
PheGenI | rs9351104 |
Biobank | rs9351104 |
1000 genomes | rs9351104 |
hgdp | rs9351104 |
ensembl | rs9351104 |
geneview | rs9351104 |
scholar | rs9351104 |
rs9351104 | |
pharmgkb | rs9351104 |
gwascentral | rs9351104 |
openSNP | rs9351104 |
23andMe | rs9351104 |
SNPshot | rs9351104 |
SNPdbe | rs9351104 |
MSV3d | rs9351104 |
GWAS Ctlg | rs9351104 |
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 | 4E-6 |
Odds Ratio | .06 [NR] unit increase |