rs72547517
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | CYP1A2*8 homozygote | |
| (A;G) | carrier of one CYP1A2*8 allele | |
| (G;G) | 0 | normal |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 74754904 |
| Gene | CYP1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72547517 |
| dbSNP (classic) | rs72547517 |
| ClinGen | rs72547517 |
| ebi | rs72547517 |
| HLI | rs72547517 |
| Exac | rs72547517 |
| Gnomad | rs72547517 |
| Varsome | rs72547517 |
| LitVar | rs72547517 |
| Map | rs72547517 |
| PheGenI | rs72547517 |
| Biobank | rs72547517 |
| 1000 genomes | rs72547517 |
| hgdp | rs72547517 |
| ensembl | rs72547517 |
| geneview | rs72547517 |
| scholar | rs72547517 |
| rs72547517 | |
| pharmgkb | rs72547517 |
| gwascentral | rs72547517 |
| openSNP | rs72547517 |
| 23andMe | rs72547517 |
| SNPshot | rs72547517 |
| SNPdbe | rs72547517 |
| MSV3d | rs72547517 |
| GWAS Ctlg | rs72547517 |
| Max Magnitude | 0 |
rs72547517, also known as 5166G>A, 5347T>C or R456H, is a SNP in the CYP1A2 gene.
The rs72547517(A) allele defines the CYP1A2*8 variant.
