rs4601326
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4601326(A;A) |
Make rs4601326(A;G) |
Make rs4601326(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 130479982 |
is a | snp |
is | mentioned by |
dbSNP | rs4601326 |
dbSNP (classic) | rs4601326 |
ClinGen | rs4601326 |
ebi | rs4601326 |
HLI | rs4601326 |
Exac | rs4601326 |
Gnomad | rs4601326 |
Varsome | rs4601326 |
LitVar | rs4601326 |
Map | rs4601326 |
PheGenI | rs4601326 |
Biobank | rs4601326 |
1000 genomes | rs4601326 |
hgdp | rs4601326 |
ensembl | rs4601326 |
geneview | rs4601326 |
scholar | rs4601326 |
rs4601326 | |
pharmgkb | rs4601326 |
gwascentral | rs4601326 |
openSNP | rs4601326 |
23andMe | rs4601326 |
SNPshot | rs4601326 |
SNPdbe | rs4601326 |
MSV3d | rs4601326 |
GWAS Ctlg | rs4601326 |
GMAF | 0.2796 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18760390] Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.