Variant (rsID / SNP)

rs2070959

UGT1A6 UGT1A10 UGT1A8 UGT1A9 UGT1A UGT1A7

rs2070959 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A6, UGT1A10, UGT1A8, UGT1A9, UGT1A, UGT1A7. Location: chromosome 2, position 234,602,191. Clinical significance in the table: Benign.

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Reference-table entries

UGT1A6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:234602191
Cytoband: 2q37.1
HGVS: NM_001072.4(UGT1A6):c.541A>G (p.Thr181Ala)
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.