rs79489631
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs79489631(A;A) |
Make rs79489631(A;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 22 |
Position | 42127545 |
Gene | CYP2D6, LOC102723722 |
is a | snp |
is | mentioned by |
dbSNP | rs79489631 |
dbSNP (classic) | rs79489631 |
ClinGen | rs79489631 |
ebi | rs79489631 |
HLI | rs79489631 |
Exac | rs79489631 |
Gnomad | rs79489631 |
Varsome | rs79489631 |
LitVar | rs79489631 |
Map | rs79489631 |
PheGenI | rs79489631 |
Biobank | rs79489631 |
1000 genomes | rs79489631 |
hgdp | rs79489631 |
ensembl | rs79489631 |
geneview | rs79489631 |
scholar | rs79489631 |
rs79489631 | |
pharmgkb | rs79489631 |
gwascentral | rs79489631 |
openSNP | rs79489631 |
23andMe | rs79489631 |
SNPshot | rs79489631 |
SNPdbe | rs79489631 |
MSV3d | rs79489631 |
GWAS Ctlg | rs79489631 |
Max Magnitude | 0 |
a variation in CYP2D6