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Variant (rsID / SNP)

rs13009407

UGT1A8

rs13009407 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A8. Location: chromosome 2, position 234,652,347. The table records no clinical significance for this variant.

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Reference-table entries

UGT1A8Not classified
Variant type
intron_variant
Chromosome / position
2:234652347
HGVS
NM_019076.5,c.856-23333C>G
Allele change
Silent

Public references

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