rs34097093
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) | 0 | common on affy axiom data |
| Make rs34097093(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 41012465 |
| Gene | CYP2B6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34097093 |
| dbSNP (classic) | rs34097093 |
| ClinGen | rs34097093 |
| ebi | rs34097093 |
| HLI | rs34097093 |
| Exac | rs34097093 |
| Gnomad | rs34097093 |
| Varsome | rs34097093 |
| LitVar | rs34097093 |
| Map | rs34097093 |
| PheGenI | rs34097093 |
| Biobank | rs34097093 |
| 1000 genomes | rs34097093 |
| hgdp | rs34097093 |
| ensembl | rs34097093 |
| geneview | rs34097093 |
| scholar | rs34097093 |
| rs34097093 | |
| pharmgkb | rs34097093 |
| gwascentral | rs34097093 |
| openSNP | rs34097093 |
| 23andMe | rs34097093 |
| SNPshot | rs34097093 |
| SNPdbe | rs34097093 |
| MSV3d | rs34097093 |
| GWAS Ctlg | rs34097093 |
| Max Magnitude | 0 |
Suspect: Variation suspected to be false positive due to artifacts of the presence of a paralogous sequence in the genome (Musumeci et al. 2010) (Sudmant et al. 2010) or evidence suggested sequencing error or computation artifacts.
| ClinVar | |
|---|---|
| Risk | Rs34097093(T;T) |
| Alt | Rs34097093(T;T) |
| Reference | Rs34097093(C;C) |
| Significance | Drug-response |
| Disease | Efavirenz response |
| Variation | info |
| Gene | CYP2B6 |
| CLNDBN | Efavirenz response |
| Reversed | 0 |
| HGVS | NC_000019.9:g.41518370C>T |
| CLNSRC | ClinVar IMU414 |
| CLNACC | RCV000133446.1, |
