Variant (rsID / SNP)

rs6759892

rs6759892 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A8, UGT1A9, UGT1A, UGT1A6, UGT1A7. Location: chromosome 2, position 234,601,669. 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: 2:234601669
Cytoband: 2q37.1
HGVS: NM_001072.4(UGT1A6):c.19T>G (p.Ser7Ala)
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.