rs746647
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs746647(C;C) |
| Make rs746647(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31146405 |
| Gene | CCHCR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs746647 |
| dbSNP (classic) | rs746647 |
| ClinGen | rs746647 |
| ebi | rs746647 |
| HLI | rs746647 |
| Exac | rs746647 |
| Gnomad | rs746647 |
| Varsome | rs746647 |
| LitVar | rs746647 |
| Map | rs746647 |
| PheGenI | rs746647 |
| Biobank | rs746647 |
| 1000 genomes | rs746647 |
| hgdp | rs746647 |
| ensembl | rs746647 |
| geneview | rs746647 |
| scholar | rs746647 |
| rs746647 | |
| pharmgkb | rs746647 |
| gwascentral | rs746647 |
| openSNP | rs746647 |
| 23andMe | rs746647 |
| SNPshot | rs746647 |
| SNPdbe | rs746647 |
| MSV3d | rs746647 |
| GWAS Ctlg | rs746647 |
| GMAF | 0.2392 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21810746] Genome-wide Association Study Identifies Variations in 6p21.3 Associated With Nevirapine-Induced Rash
[PMID 19143810
] Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.
| ClinVar | |
|---|---|
| Risk | rs746647(C;C) |
| Alt | rs746647(C;C) |
| Reference | Rs746647(T;T) |
| Significance | Drug-response |
| Disease | Nevirapine response - Toxicity/ADR |
| Variation | info |
| Gene | CCHCR1 |
| CLNDBN | nevirapine response - Toxicity/ADR |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31114182A>G |
| CLNSRC | PharmGKB Clinical Annotation |
| CLNACC | RCV000211168.1, |
