rs16864714
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16864714(C;C) |
Make rs16864714(C;T) |
Make rs16864714(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 152926122 |
is a | snp |
is | mentioned by |
dbSNP | rs16864714 |
dbSNP (classic) | rs16864714 |
ClinGen | rs16864714 |
ebi | rs16864714 |
HLI | rs16864714 |
Exac | rs16864714 |
Gnomad | rs16864714 |
Varsome | rs16864714 |
LitVar | rs16864714 |
Map | rs16864714 |
PheGenI | rs16864714 |
Biobank | rs16864714 |
1000 genomes | rs16864714 |
hgdp | rs16864714 |
ensembl | rs16864714 |
geneview | rs16864714 |
scholar | rs16864714 |
rs16864714 | |
pharmgkb | rs16864714 |
gwascentral | rs16864714 |
openSNP | rs16864714 |
23andMe | rs16864714 |
SNPshot | rs16864714 |
SNPdbe | rs16864714 |
MSV3d | rs16864714 |
GWAS Ctlg | rs16864714 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 2E-9 |
Odds Ratio | NR NR |