rs74951492
From SNPedia
Merged into | rs2856960 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs74951492(A;A) |
Make rs74951492(A;G) |
Reference | GRCh37.p5 37.3/135 |
Chromosome | 22 |
Position | 42527224 |
Gene | CYP2D6 |
is a | snp |
is | mentioned by |
dbSNP | rs74951492 |
dbSNP (classic) | rs74951492 |
ClinGen | rs74951492 |
ebi | rs74951492 |
HLI | rs74951492 |
Exac | rs74951492 |
Gnomad | rs74951492 |
Varsome | rs74951492 |
LitVar | rs74951492 |
Map | rs74951492 |
PheGenI | rs74951492 |
Biobank | rs74951492 |
1000 genomes | rs74951492 |
hgdp | rs74951492 |
ensembl | rs74951492 |
geneview | rs74951492 |
scholar | rs74951492 |
rs74951492 | |
pharmgkb | rs74951492 |
gwascentral | rs74951492 |
openSNP | rs74951492 |
23andMe | rs74951492 |
SNPshot | rs74951492 |
SNPdbe | rs74951492 |
MSV3d | rs74951492 |
GWAS Ctlg | rs74951492 |
Status | Merged into rs2856960 |
Max Magnitude | 0 |
a variation in CYP2D6