Variant (rsID / SNP)

rs6742078

rs6742078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A1. Location: chromosome 2, position 234,672,639. Clinical significance in the table: Benign; association.

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Reference-table entries

UGT1A1Benign

Clinical significance (as recorded): Benign; association
Variant type: single nucleotide variant
Chromosome / position: 2:234672639
Cytoband: 2q37.1
HGVS: NM_000463.3(UGT1A1):c.864+2842G>T
Allele change: Silent

Associated conditions / phenotypes

Bilirubin, serum level of, quantitative trait locus 1|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.