rs55889066
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | CYP1A2*5 homozygote | |
(A;G) | carrier of one CYP1A2*5 allele | |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 74753234 |
Gene | CYP1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs55889066 |
dbSNP (classic) | rs55889066 |
ClinGen | rs55889066 |
ebi | rs55889066 |
HLI | rs55889066 |
Exac | rs55889066 |
Gnomad | rs55889066 |
Varsome | rs55889066 |
LitVar | rs55889066 |
Map | rs55889066 |
PheGenI | rs55889066 |
Biobank | rs55889066 |
1000 genomes | rs55889066 |
hgdp | rs55889066 |
ensembl | rs55889066 |
geneview | rs55889066 |
scholar | rs55889066 |
rs55889066 | |
pharmgkb | rs55889066 |
gwascentral | rs55889066 |
openSNP | rs55889066 |
23andMe | rs55889066 |
SNPshot | rs55889066 |
SNPdbe | rs55889066 |
MSV3d | rs55889066 |
GWAS Ctlg | rs55889066 |
Max Magnitude | 0 |
rs55889066, also known as 3497G>A or C406Y, is a SNP in the CYP1A2 gene.
The rs55889066(A) allele defines the CYP1A2*5 variant.