Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000068.8:g.111311779C>A | variant | SNP
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NC_000068.8:g.111312829T>G | variant | SNP
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NC_000068.8:g.111312871C>T | variant | SNP
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NC_000068.8:g.111313275A>G | variant | SNP
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NC_000068.8:g.111313482G>A | variant | SNP
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NC_000068.8:g.111313537G>T | variant | SNP
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NC_000068.8:g.111313599G>A | variant | SNP
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NC_000068.8:g.111312022A>G | variant | SNP
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NC_000068.8:g.111313555C>T | variant | SNP
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NC_000068.8:g.111313559A>T | variant | SNP
|