Variant (rsID / SNP)
rs2231142
rs2231142 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCG2. Location: chromosome 4, position 89,052,323. Clinical significance in the table: drug response.
Reference-table entries
ABCG2Drug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:89052323
- Cytoband
- 4q22.1
- HGVS
- NM_004827.3(ABCG2):c.421C>A (p.Gln141Lys)
- Allele change
- Missense_Q141K
Associated conditions / phenotypes
Uric acid concentration, serum, quantitative trait locus 1|Blood group, Junior system|rosuvastatin response - Efficacy|Neoplasm of ovary|Gemcitabine response|rosuvastatin response - Metabolism/PK
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.