Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs182044780

SLCO1B3

rs182044780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B3. The table records no clinical significance for this variant.

Public references

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