rs7331194
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7331194(C;C) |
Make rs7331194(C;G) |
Make rs7331194(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 105448044 |
is a | snp |
is | mentioned by |
dbSNP | rs7331194 |
dbSNP (classic) | rs7331194 |
ClinGen | rs7331194 |
ebi | rs7331194 |
HLI | rs7331194 |
Exac | rs7331194 |
Gnomad | rs7331194 |
Varsome | rs7331194 |
LitVar | rs7331194 |
Map | rs7331194 |
PheGenI | rs7331194 |
Biobank | rs7331194 |
1000 genomes | rs7331194 |
hgdp | rs7331194 |
ensembl | rs7331194 |
geneview | rs7331194 |
scholar | rs7331194 |
rs7331194 | |
pharmgkb | rs7331194 |
gwascentral | rs7331194 |
openSNP | rs7331194 |
23andMe | rs7331194 |
SNPshot | rs7331194 |
SNPdbe | rs7331194 |
MSV3d | rs7331194 |
GWAS Ctlg | rs7331194 |
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 | 4E-6 |
Odds Ratio | .06 [NR] unit increase |