Variant (rsID / SNP)

rs4794136

rs4794136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XYLT2. Location: chromosome 17, position 48,433,958. The table records no clinical significance for this variant.

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Reference-table entries

XYLT2Not classified

Variant type: synonymous_variant
Chromosome / position: 17:48433958
HGVS: NM_022167.4,c.1569T>C,p.Tyr523Tyr
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.