Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000067.7:g.23284385G>A | variant | SNP
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NC_000067.7:g.23284331T>C | variant | SNP
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NC_000067.7:g.23284405C>T | variant | SNP
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NC_000067.7:g.23284375G>T | variant | SNP
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NC_000067.7:g.23284394T>C | variant | SNP
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NC_000067.7:g.23284353C>T | variant | SNP
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NC_000067.7:g.23284382C>T | variant | SNP
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NC_000067.7:g.23284328C>T | variant | SNP
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NC_000067.7:g.23284403C>G | variant | SNP
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NC_000067.7:g.23284406T>C | variant | SNP
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