Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000079.7:g.108635017G>A | variant | SNP
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NC_000079.7:g.108634972G>A | variant | SNP
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NC_000079.7:g.108635048C>A | variant | SNP
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NC_000079.7:g.108635001G>A | variant | SNP
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NC_000079.7:g.108634956C>T | variant | SNP
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NC_000079.7:g.108634971T>C | variant | SNP
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NC_000079.7:g.108635034A>G | variant | SNP
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NC_000079.7:g.108635063T>C | variant | SNP
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NC_000079.7:g.108634991T>C | variant | SNP
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