rs1903989
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1903989(A;A) |
Make rs1903989(A;C) |
Make rs1903989(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 52010479 |
Gene | PRKG1 |
is a | snp |
is | mentioned by |
dbSNP | rs1903989 |
dbSNP (classic) | rs1903989 |
ClinGen | rs1903989 |
ebi | rs1903989 |
HLI | rs1903989 |
Exac | rs1903989 |
Gnomad | rs1903989 |
Varsome | rs1903989 |
LitVar | rs1903989 |
Map | rs1903989 |
PheGenI | rs1903989 |
Biobank | rs1903989 |
1000 genomes | rs1903989 |
hgdp | rs1903989 |
ensembl | rs1903989 |
geneview | rs1903989 |
scholar | rs1903989 |
rs1903989 | |
pharmgkb | rs1903989 |
gwascentral | rs1903989 |
openSNP | rs1903989 |
23andMe | rs1903989 |
SNPshot | rs1903989 |
SNPdbe | rs1903989 |
MSV3d | rs1903989 |
GWAS Ctlg | rs1903989 |
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 | 1E-9 |
Odds Ratio | NR NR |