5) The SNP is common, but variable - ranges from 0% in Black populations up to >50% in East Asian populations, and everywhere in between. 6) SNP may link gyn pathology risk (incr risk with variant allele) to outcomes disparities (diff tumor biology in our work)

We're charging ahead on this work, modeling the SNP in ovarian/gyn contexts in vitro and in vivo to learn more about how diff variant allele freq corresponds to diff gyn cancer biology and poor outcomes! Need to write the grants for the lobular half of the story now... 😅