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See other CYP1A2 GT Assays ›
SNP ID:
rs2069514
Gene
CYP1A2
Gene Name
Set Membership:
> DME > Validated > Inventoried
Chromosome Location:
Chr.15: 74745879 - 74745879 on Build GRCh38
Polymorphism:
G/A, Transition substitution
Context Sequence [VIC/FAM]:

TGGCTCACCGCAACCTCCGCCTCTC[G/A]GATTCAAGCAATTGTCATGCCCCAG

Assay ID C__15859191_30
Size VIC-FAM | 150 rxns
Availability Inventoried
Catalog # 4362691
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 124060

Literature Links:

 CYP1A2 PubMed Links

Allele Nomenclature:

 CYP1A2*1L,g.-3860G>A CYP1A2*1C,g.-3860G>A

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.21)
(0.79)
Caucasian
A (0.02)
(0.98)
CEPH (CEU) - Not Available
EAS
A (0.28)
(0.72)
African American
A (0.29)
(0.71)
YRI (Yoruba) - Not Available
SAS
A (0.08)
(0.92)
Japanese
A (0.15)
(0.85)
CHB (Han Chinese) - Not Available
AFR
A (0.31)
(0.69)
Chinese
A (0.27)
(0.73)
JPT (Japanese) - Not Available
EUR
A (0.02)
(0.98)
AMR
A (0.36)
(0.64)
CYP1A2 - cytochrome P450 family 1 subfamily A member 2
There are no transcripts associated with this gene.

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More Information


Set Membership:

 DME Validated Inventoried

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