rs1958581
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1958581(C;C) |
Make rs1958581(C;G) |
Make rs1958581(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 14 |
Position | 34332393 |
is a | snp |
is | mentioned by |
dbSNP | rs1958581 |
dbSNP (classic) | rs1958581 |
ClinGen | rs1958581 |
ebi | rs1958581 |
HLI | rs1958581 |
Exac | rs1958581 |
Gnomad | rs1958581 |
Varsome | rs1958581 |
LitVar | rs1958581 |
Map | rs1958581 |
PheGenI | rs1958581 |
Biobank | rs1958581 |
1000 genomes | rs1958581 |
hgdp | rs1958581 |
ensembl | rs1958581 |
geneview | rs1958581 |
scholar | rs1958581 |
rs1958581 | |
pharmgkb | rs1958581 |
gwascentral | rs1958581 |
openSNP | rs1958581 |
23andMe | rs1958581 |
SNPshot | rs1958581 |
SNPdbe | rs1958581 |
MSV3d | rs1958581 |
GWAS Ctlg | rs1958581 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 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 | .14 [NR] unit decrease |