rs4512366
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4512366(A;A) |
Make rs4512366(A;G) |
Make rs4512366(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 124447478 |
is a | snp |
is | mentioned by |
dbSNP | rs4512366 |
dbSNP (classic) | rs4512366 |
ClinGen | rs4512366 |
ebi | rs4512366 |
HLI | rs4512366 |
Exac | rs4512366 |
Gnomad | rs4512366 |
Varsome | rs4512366 |
LitVar | rs4512366 |
Map | rs4512366 |
PheGenI | rs4512366 |
Biobank | rs4512366 |
1000 genomes | rs4512366 |
hgdp | rs4512366 |
ensembl | rs4512366 |
geneview | rs4512366 |
scholar | rs4512366 |
rs4512366 | |
pharmgkb | rs4512366 |
gwascentral | rs4512366 |
openSNP | rs4512366 |
23andMe | rs4512366 |
SNPshot | rs4512366 |
SNPdbe | rs4512366 |
MSV3d | rs4512366 |
GWAS Ctlg | rs4512366 |
GMAF | 0.1635 |
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.