New List of Genetic Variants in Simons Searchlight

We’ve published a new list of genetic variants in Simons Searchlight. This list includes 2,808 individuals with a genetic condition – that’s 739 more than the last release in August 2022! Additionally, there are new genetic communities on the list with enough people to be released to the research community. This includes 28 NEW genetic conditions:

• 2p16.3 deletion
• 15q11.2 BP1-BP2 deletion
• 17q12 duplication
• BRSK2
• CLCN4
• CSDE1
• CTBP1
• DLG4
• DYNC1H1
• EIF3F
• GIGYF1
• HECW2
• KMT5B
• MEF2C
• NEXMIF
• SCN1A
• SMARCA4
• SMARCC2
• SOX5
• TCF20
• TRIO
• UPF3B
• USP9X

This is YOUR accomplishment in helping to expand participation in Simons Searchlight. Keep reading.