Gene entry
SLCO1B3
solute carrier organic anion transporter family member 1B3
- Chromosome
- 12
- Cytoband
- 12p12.2
- Variants (rsID)
- 58
SLCO1B3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12p12.2). Its official name is “solute carrier organic anion transporter family member 1B3”. The reference table lists 58 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs143827641Benignsingle nucleotide variantRotor syndrome
- rs3764006Benignsingle nucleotide variantRotor syndrome
- rs4149117Benignsingle nucleotide variantRotor syndrome
- rs7311358Benignsingle nucleotide variantRotor syndrome
- rs145334570Conflicting interpretationssingle nucleotide variantRotor syndrome
- rs180875376Conflicting interpretationssingle nucleotide variantRotor syndrome
- rs146780296Uncertain significancesingle nucleotide variantRotor syndrome
Other listed variants
- rs1304539
- rs1356148
- rs2033515
- rs2417886
- rs2417940
- rs4149118
- rs4149126
- rs4149146
- rs4469945
- rs6487175
- rs7977213
- rs10770742
- rs10841661
- rs10841697
- rs11045524
- rs11045545
- rs11045577
- rs11045585
- rs11045595
- rs11494550
- rs12824715
- rs12826576
- rs17674149
- rs34518138
- rs74588265
- rs75008118
- rs75956016
- rs76331226
- rs77105479
- rs77406826
- rs117239853
- rs117246001
- rs117309110
- rs117428098
- rs138300728
- rs142264776
- rs147555114
- rs149434472
- rs150007972
- rs180699430
- rs182044780
- rs185865142
- rs189315032
- rs189943255
- rs201071326
- rs529665684
- rs537672413
- rs546036152
- rs555200331
- rs560166567
- rs564303378
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.