rs78209835
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs78209835(A;A) |
Make rs78209835(A;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 22 |
Position | 42127611 |
Gene | CYP2D6, LOC102723722 |
is a | snp |
is | mentioned by |
dbSNP | rs78209835 |
dbSNP (classic) | rs78209835 |
ClinGen | rs78209835 |
ebi | rs78209835 |
HLI | rs78209835 |
Exac | rs78209835 |
Gnomad | rs78209835 |
Varsome | rs78209835 |
LitVar | rs78209835 |
Map | rs78209835 |
PheGenI | rs78209835 |
Biobank | rs78209835 |
1000 genomes | rs78209835 |
hgdp | rs78209835 |
ensembl | rs78209835 |
geneview | rs78209835 |
scholar | rs78209835 |
rs78209835 | |
pharmgkb | rs78209835 |
gwascentral | rs78209835 |
openSNP | rs78209835 |
23andMe | rs78209835 |
SNPshot | rs78209835 |
SNPdbe | rs78209835 |
MSV3d | rs78209835 |
GWAS Ctlg | rs78209835 |
GMAF | 0.001377 |
Max Magnitude | 0 |
a variation in CYP2D6