Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000084.7:g.52287593T>G | variant | SNP
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NC_000084.7:g.52287614T>G | variant | SNP
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NC_000084.7:g.52287647T>C | variant | SNP
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NC_000084.7:g.52287592C>T | variant | SNP
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NC_000084.7:g.52287623A>C | variant | SNP
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NC_000084.7:g.52287663C>T | variant | SNP
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NC_000084.7:g.52287637T>G | variant | SNP
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NC_000084.7:g.52287586A>G | variant | SNP
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NC_000084.7:g.52287674G>A | variant | SNP
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