Variant (rsID / SNP)

rs11045852

rs11045852 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B1. Location: chromosome 12, position 21,349,885. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLCO1B1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:21349885
Cytoband: 12p12.1
HGVS: NM_006446.5(SLCO1B1):c.733A>G (p.Ile245Val)
Allele change: Missense_I245V

Associated conditions / phenotypes

Rotor syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.