Variant (rsID / SNP)

rs7311358

rs7311358 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1B3. Location: chromosome 12, position 21,015,760. Clinical significance in the table: Benign.

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Reference-table entries

SLCO1B3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:21015760
Cytoband: 12p12.2
HGVS: NM_019844.4(SLCO1B3):c.699G>A (p.Met233Ile)
Allele change: Missense_M233I

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.