Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1000737

MCTP2

rs1000737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCTP2. 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.