Rare variant imputation with the TOPMed reference panel combined with whole-genome sequence data in 52,658 type 2 diabetes cases and 381,683 controls identifies novel rare variant associations and informs the spectrum of pathogenicity in monogenic diabete
| Lead Author | |
|---|---|
| Name of Professional Meeting |
ASHG - American Society of Human Genetics Annual Meeting
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| Date(s) of Professional Meeting |
November 1-5, 2023
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| Program Number/Abstract ID |
2023-A-2054-ASHG
|