Dear team,
As mentioned in your blog, I understand that subsets based on specific cohorts from gnomAD v4 will not be provided. Given this, may I kindly request your assistance in checking the distribution of a small set of variants for clinical purposes? I am particularly interested in determining whether these variants are part of the IBD cohorts contributing to gnomAD v4.
Would you be able to help with this as a matter of urgency? Your support would be greatly appreciated.
Thank you very much for your time and consideration.