Variant (rsID / SNP)
rs4148323
COVERS 10 GENEScovers 10 genes
rs4148323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COVERS 10 GENES, covers 10 genes. Location: chromosome 2, position 234,669,144. Clinical significance in the table: Conflicting interpretations of pathogenicity; drug response.
Reference-table entries
COVERS 10 GENESConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity; drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:234669144
- Cytoband
- 2q37.1
- HGVS
- UGT1A1*6
- Allele change
- Silent
Associated conditions / phenotypes
Gilbert syndrome|Bilirubin, serum level of, quantitative trait locus 1|Lucey-Driscoll syndrome|Irinotecan response|Crigler-Najjar syndrome, type II
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.