Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs61744730

PTH2R

rs61744730 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTH2R. 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.