rs62625688
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs62625688(A;G) |
Make rs62625688(G;G) |
Reference | GRCh37 37.1/132 |
Chromosome | 22 |
Position | 42131915 |
Gene | CYP2D6, LOC102723722, LOC107984152, LOC107987465, LOC107987477, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs62625688 |
dbSNP (classic) | rs62625688 |
ClinGen | rs62625688 |
ebi | rs62625688 |
HLI | rs62625688 |
Exac | rs62625688 |
Gnomad | rs62625688 |
Varsome | rs62625688 |
LitVar | rs62625688 |
Map | rs62625688 |
PheGenI | rs62625688 |
Biobank | rs62625688 |
1000 genomes | rs62625688 |
hgdp | rs62625688 |
ensembl | rs62625688 |
geneview | rs62625688 |
scholar | rs62625688 |
rs62625688 | |
pharmgkb | rs62625688 |
gwascentral | rs62625688 |
openSNP | rs62625688 |
23andMe | rs62625688 |
SNPshot | rs62625688 |
SNPdbe | rs62625688 |
MSV3d | rs62625688 |
GWAS Ctlg | rs62625688 |
Max Magnitude | 0 |
a variation in CYP2D6