The Challenge of Genetic Variants of Uncertain Clinical Significance is a research paper published in Annals of Internal Medicine (2022). On theSindex it has a DataRank of 0. It has been cited 158 times.
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NHGRI NIH HHS
Grant: R01 HG010365
NHGRI NIH HHS
Grant: RM1 HG007257
FWCI
17.48
Citation Percentile
1.0%
Citation Trend
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Additional file 1 of Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive cases
Additional file 1 of Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive cases
Additional file 2 of mutscan—a flexible R package for efficient end-to-end analysis of multiplexed assays of variant effect data
Additional file 2 of mutscan—a flexible R package for efficient end-to-end analysis of multiplexed assays of variant effect data
Additional file 3 of mutscan—a flexible R package for efficient end-to-end analysis of multiplexed assays of variant effect data
Additional file 3 of mutscan—a flexible R package for efficient end-to-end analysis of multiplexed assays of variant effect data
Additional file 1 of mutscan—a flexible R package for efficient end-to-end analysis of multiplexed assays of variant effect data
Additional file 1 of mutscan—a flexible R package for efficient end-to-end analysis of multiplexed assays of variant effect data