Variant (rsID / SNP)

rs17864686

rs17864686 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A8. Location: chromosome 2, position 234,591,339. Clinical significance in the table: Benign.

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Reference-table entries

UGT1A8Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:234591339
Cytoband: 2q37.1
HGVS: NM_019076.5(UGT1A8):c.855+64131G>A
Allele change: Silent

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.