rs74478221
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs74478221(A;A) |
Make rs74478221(A;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 22 |
Position | 42126624 |
Gene | CYP2D6 |
is a | snp |
is | mentioned by |
dbSNP | rs74478221 |
dbSNP (classic) | rs74478221 |
ClinGen | rs74478221 |
ebi | rs74478221 |
HLI | rs74478221 |
Exac | rs74478221 |
Gnomad | rs74478221 |
Varsome | rs74478221 |
LitVar | rs74478221 |
Map | rs74478221 |
PheGenI | rs74478221 |
Biobank | rs74478221 |
1000 genomes | rs74478221 |
hgdp | rs74478221 |
ensembl | rs74478221 |
geneview | rs74478221 |
scholar | rs74478221 |
rs74478221 | |
pharmgkb | rs74478221 |
gwascentral | rs74478221 |
openSNP | rs74478221 |
23andMe | rs74478221 |
SNPshot | rs74478221 |
SNPdbe | rs74478221 |
MSV3d | rs74478221 |
GWAS Ctlg | rs74478221 |
Max Magnitude | 0 |
a variation in CYP2D6