| Geno
|
Mag
|
Summary
|
| (C;C)
|
|
CYP1A2_1545T>C homozygote
|
| (C;T)
|
|
carrier of one CYP1A2_1545T>C allele
|
| (T;T)
|
0
|
normal
|
| ? | (C;C) (C;T) (T;T) | 28 |
|---|
 |
is a SNP in the
CYP1A2 gene.
The rs2470890(C) allele defines the CYP1A2_1545T>C variant.
[PMID 21281405] Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson's disease
[PMID 18992148] Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.
| GET Evidence
|
| rs2470890
|
| aa_change
|
|
| aa_change_short
|
|
| impact
|
pharmacogenetic
|
| qualified_impact
|
Insufficiently evaluated pharmacogenetic
|
| overall_frequency
|
0.471556
|
| summary
|
|
