uni studies use PCR-RFLP or TaqMan assays to target this SNP
then there's obv whole exome/genome sequencing
and a single gene test, a doc can order IGF1R gene sequencing for growth disorders
if you're homozygous (AA) for IGF1 signaling, the minor allele A of rs2229765 reduces receptor function
its a 3' UTR variant. it alters microRNA binding which leads to less IGF1R expression on cell surface
so as a result your cells have lower IGF1R density
your IGF1 signaling cascade is blunted
its linked to lower serum IGF1 levels and more IGF1 bioavailability. the circulating IGF1 will be higher in your blood because there are fewer receptors to clear it
so basically you'll have a hyporesponsive IGF1R
your IGF1 signaling will be lower than someone with GG genotype