Association details of variants in WDR89.
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WDR89 (at the GRCh38 genomic location of chr14:63597039–63641871) was identified from a SKAT-O analysis of high/moderate impact variants. 7 missense variants in WDR89 have a result in the primary unfiltered GWAS. Amino Acid change is depicted in the HGVS (Human Genome Variation Society) notation. (XLSX)
创建时间：
2024-03-22
