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NCBI ALFA
Aggregate population allele frequency data from dbGap studies: millions of subjects, millions of variants, trillions of genotypes.
Frequency for different ancestry populations: compare frequency across populations, filter common and rare variants, variant interpretation.
Integrated with dbSNP annotation including: RefSeq Genomic, mRNA, and protein, ClinVar clinical significance and PubMed literature.
Open-access and FAIR compliance: findable, accessible, interoperable, reusable.
Visit our project page for more information: go.usa.gov/xGV8h
NIH, National Library of Medicine
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2022/06/13求める情報が見つからない場合は、キーワードや指定した条件を変えてみてください。