Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs3826200

PRDM7

rs3826200 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM7. 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.