Variant (rsID / SNP)
rs4149057
rs4149057 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B1. Location: chromosome 12, position 21,331,599. Clinical significance in the table: Benign.
Reference-table entries
SLCO1B1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:21331599
- Cytoband
- 12p12.1
- HGVS
- NM_006446.5(SLCO1B1):c.571T>C (p.Leu191=)
- Allele change
- Synonymous_L191L
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.