Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs35350960

UGT1A1

rs35350960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A1. Location: chromosome 2, position 234,669,619. Clinical significance in the table: Conflicting interpretations of pathogenicity; other.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

UGT1A1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity; other
Variant type
single nucleotide variant
Chromosome / position
2:234669619
Cytoband
2q37.1
HGVS
NM_000463.3(UGT1A1):c.686C>A (p.Pro229Gln)
Allele change
Silent

Associated conditions / phenotypes

Gilbert syndrome|Crigler-Najjar syndrome, type II

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.