Variant (rsID / SNP)

rs4124874

rs4124874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A1. Location: chromosome 2, position 234,665,659. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

UGT1A1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 2:234665659
Cytoband: 2q37.1
HGVS: NM_001072.4(UGT1A6):c.862-10021T>G
Allele change: Silent

Associated conditions / phenotypes

Gilbert syndrome, susceptibility to|Gilbert 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.