Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs4287068

FAM199X

rs4287068 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM199X. 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.