rs74966855
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs74966855(A;A) |
Make rs74966855(A;C) |
Reference | GRCh37 37.1/132 |
Chromosome | 22 |
Position | 42131289 |
Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs74966855 |
dbSNP (classic) | rs74966855 |
ClinGen | rs74966855 |
ebi | rs74966855 |
HLI | rs74966855 |
Exac | rs74966855 |
Gnomad | rs74966855 |
Varsome | rs74966855 |
LitVar | rs74966855 |
Map | rs74966855 |
PheGenI | rs74966855 |
Biobank | rs74966855 |
1000 genomes | rs74966855 |
hgdp | rs74966855 |
ensembl | rs74966855 |
geneview | rs74966855 |
scholar | rs74966855 |
rs74966855 | |
pharmgkb | rs74966855 |
gwascentral | rs74966855 |
openSNP | rs74966855 |
23andMe | rs74966855 |
SNPshot | rs74966855 |
SNPdbe | rs74966855 |
MSV3d | rs74966855 |
GWAS Ctlg | rs74966855 |
Max Magnitude | 0 |
a variation in CYP2D6