SLCO1B1

solute carrier organic anion transporter family member 1B1
OMIM: 604843, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green SLCO1B1 in Mendeliome


Version 2.0

2 reviews Other
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperbilirubinemia, Rotor type, digenic 237450

Green SLCO1B1 in Haem degradation and bilirubin metabolism defects


Level 2: Metabolic disorders
Version 1.0

0 reviews Other
Sources
  • Expert Review Green
Phenotypes
  • Rotor syndrome MONDO:0009379 (MIM#237450), Disorders of bilirubin metabolism and biliary transport

No list SLCO1B1 in Pharmacogenomics_Paediatric


Level 2: Screening
Version 1.0

1 review Other
Sources
  • Other
Phenotypes
  • Risk for simvastatin-induced myopathy

Red SLCO1B1 in Additional findings_Paediatric


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Hyperbilirubinemia, Rotor type, digenic

Red SLCO1B1 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Hyperbilirubinemia, Rotor type, digenic

Green SLCO1B1 in Transplant Co-Morbidity


Level 2: Screening
Version 1.0

1 review Other
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Hyperbilirubinemia, Rotor type, digenic MIM# 237450