Variant (rsID / SNP)

rs59113707

rs59113707 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B1. Location: chromosome 12, position 21,355,489. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLCO1B1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:21355489
Cytoband: 12p12.1
HGVS: NM_006446.5(SLCO1B1):c.1200C>G (p.Phe400Leu)
Allele change: Missense_F400L

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.