Gene | Association | Disease Qualifier | Disease | Evidence | Source | Based On | References |
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Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000082.7:g.13288972A>C | variant | SNP
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NC_000082.7:g.13288984G>A | variant | SNP
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