Variant (rsID / SNP)

rs1845555

rs1845555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT2B4. Location: chromosome 4, position 70,355,211. The table records no clinical significance for this variant.

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Reference-table entries

UGT2B4Not classified

Variant type: synonymous_variant
Chromosome / position: 4:70355211
HGVS: NM_021139.3,c.948A>G,p.Thr316Thr
Allele change: Synonymous_T180T

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.