Variant (rsID / SNP)

rs4148301

rs4148301 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT2A2, UGT2A1. Location: chromosome 4, position 70,462,042. The table records no clinical significance for this variant.

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Reference-table entries

UGT2A2Not classified

Variant type: missense_variant
Chromosome / position: 4:70462042
HGVS: NM_001105677.2,c.949G>A,p.Gly317Arg
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.