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_000072.7:g.28985386T>G | variant | SNP
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NC_000072.7:g.28983204G>A | variant | SNP
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NC_000072.7:g.28983738C>T | variant | SNP
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NC_000072.7:g.28986377G>A | variant | SNP
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NC_000072.7:g.28990190A>G | variant | SNP
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NC_000072.7:g.28990199A>G | variant | SNP
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NC_000072.7:g.28990232G>A | variant | SNP
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NC_000072.7:g.28990258A>T | variant | SNP
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NC_000072.7:g.28989329T>C | variant | SNP
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NC_000072.7:g.28989362A>G | variant | SNP
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