Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs74593128

MMS22L

rs74593128 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMS22L. 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.