rs787274
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs787274(A;A) |
Make rs787274(A;C) |
Make rs787274(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 112788083 |
Gene | SNX30 |
is a | snp |
is | mentioned by |
dbSNP | rs787274 |
dbSNP (classic) | rs787274 |
ClinGen | rs787274 |
ebi | rs787274 |
HLI | rs787274 |
Exac | rs787274 |
Gnomad | rs787274 |
Varsome | rs787274 |
LitVar | rs787274 |
Map | rs787274 |
PheGenI | rs787274 |
Biobank | rs787274 |
1000 genomes | rs787274 |
hgdp | rs787274 |
ensembl | rs787274 |
geneview | rs787274 |
scholar | rs787274 |
rs787274 | |
pharmgkb | rs787274 |
gwascentral | rs787274 |
openSNP | rs787274 |
23andMe | rs787274 |
SNPshot | rs787274 |
SNPdbe | rs787274 |
MSV3d | rs787274 |
GWAS Ctlg | rs787274 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 7E-10 |
Odds Ratio | NR NR |