Variant (rsID / SNP)

rs143827641

rs143827641 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B3. Location: chromosome 12, position 21,054,393. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLCO1B3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:21054393
Cytoband: 12p12.2
HGVS: NM_019844.4(SLCO1B3):c.1857A>T (p.Val619=)
Allele change: Synonymous_V619V

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.