rs3765212
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3765212(G;G) |
Make rs3765212(G;T) |
Make rs3765212(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 123438124 |
Gene | WDYHV1 |
is a | snp |
is | mentioned by |
dbSNP | rs3765212 |
dbSNP (classic) | rs3765212 |
ClinGen | rs3765212 |
ebi | rs3765212 |
HLI | rs3765212 |
Exac | rs3765212 |
Gnomad | rs3765212 |
Varsome | rs3765212 |
LitVar | rs3765212 |
Map | rs3765212 |
PheGenI | rs3765212 |
Biobank | rs3765212 |
1000 genomes | rs3765212 |
hgdp | rs3765212 |
ensembl | rs3765212 |
geneview | rs3765212 |
scholar | rs3765212 |
rs3765212 | |
pharmgkb | rs3765212 |
gwascentral | rs3765212 |
openSNP | rs3765212 |
23andMe | rs3765212 |
SNPshot | rs3765212 |
SNPdbe | rs3765212 |
MSV3d | rs3765212 |
GWAS Ctlg | rs3765212 |
GMAF | 0.3843 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 18760390] Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.