Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs12927688

XYLT1

rs12927688 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XYLT1. The table records no clinical significance for this variant.

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.