rs72547516
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | normal |
(A;T) | carrier of one CYP1A2*4 allele | |
(T;T) | CYP1A2*4 homozygote |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 74752237 |
Gene | CYP1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs72547516 |
dbSNP (classic) | rs72547516 |
ClinGen | rs72547516 |
ebi | rs72547516 |
HLI | rs72547516 |
Exac | rs72547516 |
Gnomad | rs72547516 |
Varsome | rs72547516 |
LitVar | rs72547516 |
Map | rs72547516 |
PheGenI | rs72547516 |
Biobank | rs72547516 |
1000 genomes | rs72547516 |
hgdp | rs72547516 |
ensembl | rs72547516 |
geneview | rs72547516 |
scholar | rs72547516 |
rs72547516 | |
pharmgkb | rs72547516 |
gwascentral | rs72547516 |
openSNP | rs72547516 |
23andMe | rs72547516 |
SNPshot | rs72547516 |
SNPdbe | rs72547516 |
MSV3d | rs72547516 |
GWAS Ctlg | rs72547516 |
Max Magnitude | 0 |
rs72547516, also known as 2499A>T or I386F, is a SNP in the CYP1A2 gene.
The rs72547516(T) allele defines the CYP1A2*4 variant.