Variant (rsID / SNP)

rs199775914

rs199775914 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT8. Location: chromosome 4, position 115,544,847. Clinical significance in the table: Uncertain significance.

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Reference-table entries

UGT8Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:115544847
Cytoband: 4q26
HGVS: NM_001128174.3(UGT8):c.811C>T (p.Pro271Ser)
Allele change: Missense_P271S

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.