Variant (rsID / SNP)
rs77271279
rs77271279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B1. Location: chromosome 12, position 21,329,832. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
SLCO1B1Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:21329832
- Cytoband
- 12p12.1
- HGVS
- NM_006446.5(SLCO1B1):c.481+1G>T
- Allele change
- Silent
Associated conditions / phenotypes
Rotor syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.