rs80262685
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs80262685(A;G) |
Make rs80262685(G;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 22 |
Position | 42128576 |
Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs80262685 |
dbSNP (classic) | rs80262685 |
ClinGen | rs80262685 |
ebi | rs80262685 |
HLI | rs80262685 |
Exac | rs80262685 |
Gnomad | rs80262685 |
Varsome | rs80262685 |
LitVar | rs80262685 |
Map | rs80262685 |
PheGenI | rs80262685 |
Biobank | rs80262685 |
1000 genomes | rs80262685 |
hgdp | rs80262685 |
ensembl | rs80262685 |
geneview | rs80262685 |
scholar | rs80262685 |
rs80262685 | |
pharmgkb | rs80262685 |
gwascentral | rs80262685 |
openSNP | rs80262685 |
23andMe | rs80262685 |
SNPshot | rs80262685 |
SNPdbe | rs80262685 |
MSV3d | rs80262685 |
GWAS Ctlg | rs80262685 |
GMAF | 0.0326 |
Max Magnitude | 0 |
a variation in CYP2D6