Variant (rsID / SNP)

rs11098261

rs11098261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT8. Location: chromosome 4, position 115,589,302. The table records no clinical significance for this variant.

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Reference-table entries

UGT8Not classified

Variant type: missense_variant
Chromosome / position: 4:115589302
HGVS: NM_001128174.3,c.1104A>G,p.Ile368Met
Allele change: Missense_I368M

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.