FAIRsharing record for: Genome Variation Allele Frequencies Worldwide
收藏DataCite Commons2025-03-24 更新2025-04-15 收录
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https://fairsharing.org/10.25504/FAIRsharing.b2abc2
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This FAIRsharing record describes: FINDbase worldwide is an online resource documenting frequencies of clinically relevant genomic variants, namely pathogenic variants leading to inherited disorders and pharmacogenomic biomarkers, in various populations worldwide. The initial data came from previously published reports as well as from unpublished information contributed from individual researchers prior of publication.
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FAIRsharing创建时间：
2025-03-24
