Rs28371706
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs28371706 |
| nextbio | rs28371706 |
| hapmap | rs28371706 |
| 1000 genomes | rs28371706 |
| hgdp | rs28371706 |
| ensembl | rs28371706 |
| gopubmed | rs28371706 |
| scholar | rs28371706 |
| rs28371706 | |
| pharmgkb | rs28371706 |
| gwascentral | rs28371706 |
| openSNP | rs28371706 |
| 23andMe | rs28371706 |
| 23andMe all | rs28371706 |
| SNP Nexus | |
| SNPshot | rs28371706 |
| SNPdbe | rs28371706 |
| MSV3d | rs28371706 |
| Gene | CYP2D6 |
| Chromosome | 22 |
| Orientation | minus |
| Position | 42525772 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | normal |
| (C;T) | Carrier of one CYP2D6 variant, possibly decreased on non-functioning. | |
| (T;T) | Homozygous for CYP2D6 variants, possibly decreased or non-functioning. |
The rs28371706(T) allele is found in several CYP2D6 variants:
- CYP2D6*17 decreased activity variant
- CYP2D6*40 non-functioning variant
- CYP2D6*58 variant
- CYP2D6*64 variant
| PharmGKB | PA161145191 |
| Name | CYP2D6:1023 C>T |
| Annotation | Variant was identified as being part of the reduced function haplotype CYP2D6*17. |
| Gene | CYP2D6 |
| Featue | Exon/NonSyn |
| Evidence | Web Resource:http://www.pharmgkb.org/search/annotatedGene/cyp2d6/variant.jsp#ImportantVariantInformationforCYP2D6-222 |
| Drugs | |
| Diseases | |
| Curation Level | In-Depth |
