rs80018788
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs80018788(A;A) |
Make rs80018788(A;C) |
Reference | GRCh37 37.1/131 |
Chromosome | 22 |
Position | 42129162 |
Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs80018788 |
dbSNP (classic) | rs80018788 |
ClinGen | rs80018788 |
ebi | rs80018788 |
HLI | rs80018788 |
Exac | rs80018788 |
Gnomad | rs80018788 |
Varsome | rs80018788 |
LitVar | rs80018788 |
Map | rs80018788 |
PheGenI | rs80018788 |
Biobank | rs80018788 |
1000 genomes | rs80018788 |
hgdp | rs80018788 |
ensembl | rs80018788 |
geneview | rs80018788 |
scholar | rs80018788 |
rs80018788 | |
pharmgkb | rs80018788 |
gwascentral | rs80018788 |
openSNP | rs80018788 |
23andMe | rs80018788 |
SNPshot | rs80018788 |
SNPdbe | rs80018788 |
MSV3d | rs80018788 |
GWAS Ctlg | rs80018788 |
Max Magnitude | 0 |
a variation in CYP2D6