Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000075.7:g.18856026A>T | variant | SNP
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NC_000075.7:g.18856140C>T | variant | SNP
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NC_000075.7:g.18856405C>T | variant | SNP
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NC_000075.7:g.18856614A>C | variant | SNP
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NC_000075.7:g.18857317A>C | variant | SNP
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NC_000075.7:g.18859147G>A | variant | SNP
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NC_000075.7:g.18859438G>A | variant | SNP
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NC_000075.7:g.18859847C>T | variant | SNP
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NC_000075.7:g.18857107C>T | variant | SNP
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NC_000075.7:g.18853882G>A | variant | SNP
|