rs62468398
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs62468398(C;C) |
Make rs62468398(C;T) |
Make rs62468398(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 132208726 |
Gene | PLXNA4 |
is a | snp |
is | mentioned by |
dbSNP | rs62468398 |
dbSNP (classic) | rs62468398 |
ClinGen | rs62468398 |
ebi | rs62468398 |
HLI | rs62468398 |
Exac | rs62468398 |
Gnomad | rs62468398 |
Varsome | rs62468398 |
LitVar | rs62468398 |
Map | rs62468398 |
PheGenI | rs62468398 |
Biobank | rs62468398 |
1000 genomes | rs62468398 |
hgdp | rs62468398 |
ensembl | rs62468398 |
geneview | rs62468398 |
scholar | rs62468398 |
rs62468398 | |
pharmgkb | rs62468398 |
gwascentral | rs62468398 |
openSNP | rs62468398 |
23andMe | rs62468398 |
SNPshot | rs62468398 |
SNPdbe | rs62468398 |
MSV3d | rs62468398 |
GWAS Ctlg | rs62468398 |
Max Magnitude | 0 |
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 | .16 [NR] unit decrease |