rs1582156
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1582156(A;A) |
Make rs1582156(A;T) |
Make rs1582156(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 195523215 |
is a | snp |
is | mentioned by |
dbSNP | rs1582156 |
dbSNP (classic) | rs1582156 |
ClinGen | rs1582156 |
ebi | rs1582156 |
HLI | rs1582156 |
Exac | rs1582156 |
Gnomad | rs1582156 |
Varsome | rs1582156 |
LitVar | rs1582156 |
Map | rs1582156 |
PheGenI | rs1582156 |
Biobank | rs1582156 |
1000 genomes | rs1582156 |
hgdp | rs1582156 |
ensembl | rs1582156 |
geneview | rs1582156 |
scholar | rs1582156 |
rs1582156 | |
pharmgkb | rs1582156 |
gwascentral | rs1582156 |
openSNP | rs1582156 |
23andMe | rs1582156 |
SNPshot | rs1582156 |
SNPdbe | rs1582156 |
MSV3d | rs1582156 |
GWAS Ctlg | rs1582156 |
Max Magnitude | 0 |
? | (A;A) (A;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 | .07 [NR] unit decrease |