rs79802111
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs79802111(C;T) |
Make rs79802111(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 22 |
Position | 42130642 |
Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs79802111 |
dbSNP (classic) | rs79802111 |
ClinGen | rs79802111 |
ebi | rs79802111 |
HLI | rs79802111 |
Exac | rs79802111 |
Gnomad | rs79802111 |
Varsome | rs79802111 |
LitVar | rs79802111 |
Map | rs79802111 |
PheGenI | rs79802111 |
Biobank | rs79802111 |
1000 genomes | rs79802111 |
hgdp | rs79802111 |
ensembl | rs79802111 |
geneview | rs79802111 |
scholar | rs79802111 |
rs79802111 | |
pharmgkb | rs79802111 |
gwascentral | rs79802111 |
openSNP | rs79802111 |
23andMe | rs79802111 |
SNPshot | rs79802111 |
SNPdbe | rs79802111 |
MSV3d | rs79802111 |
GWAS Ctlg | rs79802111 |
Max Magnitude | 0 |
a variation in CYP2D6