rs59099247
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs59099247(C;T) |
Make rs59099247(T;T) |
Reference | GRCh37 37.1/132 |
Chromosome | 22 |
Position | 42132089 |
Gene | CYP2D6, LOC102723722, LOC107984152, LOC107987465, LOC107987477, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs59099247 |
dbSNP (classic) | rs59099247 |
ClinGen | rs59099247 |
ebi | rs59099247 |
HLI | rs59099247 |
Exac | rs59099247 |
Gnomad | rs59099247 |
Varsome | rs59099247 |
LitVar | rs59099247 |
Map | rs59099247 |
PheGenI | rs59099247 |
Biobank | rs59099247 |
1000 genomes | rs59099247 |
hgdp | rs59099247 |
ensembl | rs59099247 |
geneview | rs59099247 |
scholar | rs59099247 |
rs59099247 | |
pharmgkb | rs59099247 |
gwascentral | rs59099247 |
openSNP | rs59099247 |
23andMe | rs59099247 |
SNPshot | rs59099247 |
SNPdbe | rs59099247 |
MSV3d | rs59099247 |
GWAS Ctlg | rs59099247 |
GMAF | 0.02158 |
Max Magnitude | 0 |
a variation in CYP2D6