Species | 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_051348.1:g.43644623A>G | variant | SNP
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NC_051348.1:g.43645882A>C | variant | SNP
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NC_051348.1:g.43691001C>T | variant | SNP
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NC_051348.1:g.43694812C>T | variant | SNP
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NC_051348.1:g.43697018G>C | variant | SNP
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NC_051348.1:g.43677907C>G | variant | SNP
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NC_051348.1:g.43679940C>T | variant | SNP
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NC_051348.1:g.43681246T>C | variant | SNP
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NC_051348.1:g.43667941C>T | variant | SNP
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NC_051348.1:g.43684383C>T | variant | SNP
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