P194: SeqFirst mitigates race-based disparities in access to a precise genetic diagnosis in hospitalized neonates by Wenger, Tara, Keefe, Alexandra, Kruidenier, Lukas, Sikes, Megan, Scott, Abbey, Yu, Joon-Ho, MacDuffie, Kate, Anderson, Kailyn, Sommers, Olivia, Gildersleeve, Heidi, Buckingham, Kati, Chong, Jessica, Dipple, Katrina, Veenstra, David, Doherty, Dan, Miller, Daniel, Copenheaver, Deborah, Juusola, Jane, Snook, Amy, Davis, Chayna, McWalter, Kirsty, Kruszka, Paul, Bamshad, Michael

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P214: SeqFirst DDi: Early whole genome sequencing improves access to early precise genetic diagnosis for children with developmental differences by Dipple, Katrina, Doherty, Daniel, Anderson, Kailyn, Sommers, Olivia, Wenger, Tara, MacDuffie, Kate, Keefe, Alexandra, Scott, Abbey, Kruidenier, Lukas, Love-Nichols, Jamie, Gildersleeve, Heidi, Davis, Chayna, Buckingham, Kati, Chong, Jessica, Veenstra, David, Miller, Danny, Copenheaver, Deborah, Juusola, Jane, Retterer, Kyle, McWalter, Kirsty, Kruszka, Paul, Yu, Joon-Ho, Bamshad, Michael

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Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects by Chong, Jessica X., Childers, Matthew Carter, Marvin, Colby T., Marcello, Anthony J., Gonorazky, Hernan, Hazrati, Lili-Naz, Dowling, James J., Al Amrani, Fatema, Alanay, Yasemin, Nieto, Yolanda, Gabriel, Miguel Á Marín, Aylsworth, Arthur S., Buckingham, Kati J., Shively, Kathryn M., Sommers, Olivia, Anderson, Kailyn, Regnier, Michael, Bamshad, Michael J.

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P150: ClinGen hereditary cardiovascular disease gene curation expert panel: reappraisal of the validity of hypertrophic cardiomyopathy genes by Waddell, Amber, Hespe, Sophie, Asatryan, Babken, Owens, Emma, Thaxton, Courtney, Adduru, Mhy-Lanie, Anderson, Kailyn, Brown, Emily, Hoffman-Andrews, Lily, Jordan, Elizabeth, Mayers, Megan, Peters, Stacey, Stafford, Fergus, Bagnall, Richard, Bronicki, Lucas, Callewaert, Bert, Chahal, C. Anwar, James, Cynthia, Jarinova, Olga, Landstrom, Andrew, McNally, Elizabeth, Murray, Brittney, Muiño-Mosquera, Laura, Parikh, Victoria, Reuter, Chloe, Walsh, Roddy, Wayburn, Bess, Ware, James, Ingles, Jodie

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A reference human induced pluripotent stem cell line for collaborative studies by Pantazis, CB, Yang, A, Lara, E, McDonough, JA, Blauwendraat, C, Peng, L, Oguro, H, Kanaujiya, J, Zou, J, Sebesta, D

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CFAP47 is Implicated in X-Linked Polycystic Kidney Disease by Mori, Takayasu, Fujimaru, Takuya, Liu, Chunyu, Patterson, Karynne, Yamamoto, Kouhei, Suzuki, Takefumi, Chiga, Motoko, Sekine, Akinari, Ubara, Yoshifumi, Miller, Danny E., Zalusky, Miranda P.G., Mandai, Shintaro, Ando, Fumiaki, Mori, Yutaro, Kikuchi, Hiroaki, Susa, Koichiro, Wei, Chia-Lin, Bamshad, Michael J., Eichler, Evan E., Anderson, Kailyn, Anderson, Peter, Bacus, Tamara J., Best, Sabrina, Blue, Elizabeth E., Brower, Katherine, Buckingham, Kati J., Carroll, Brianne, Casadei, Silvia, Chong, Jessica X., Damaraju, Nikhita, Davis, Colleen P., Frazar, Christian D., Gibson, Sophia, Goffena, Joy, Gordon, William W., Gustafson, Jonas A., Harvey, William T., Horike-Pyne, Martha, Hurless, Jameson R., Jacques, Caitlin, Jarvik, Gail P., Johanson, Eric, Thomas Kolar, J., Liu, Xiaomeng, Marvin, Colby T., McGee, Sean, Meyers, Holli, Miller, Danny E., Nielsen, Patrick M., Patterson, Karynne, Radhakrishnan, Aparna, Richardson, Matthew A., Ryke, Erica L., Sarkytbayeva, Aliya, Shaffer, Tristan, Shively, Kathryn M., Sommers, Olivia M., Storz, Sophie H.R., Smith, Joshua D., Starita, Lea M., Tackettl, Monica, Ward, Sydney A., Weiss, Jeffrey M., Yi, Qian, Zalusky, Miranda P.G., Mefford, Heather, Chong, Jessica X., Bamshad, Michael J., Tan, Yue-Qiu, Zhang, Feng, Uchida, Shinichi, Sohara, Eisei

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