Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000073.7:g.15680227T>C | variant | SNP
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NC_000073.7:g.15680228G>A | variant | SNP
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NC_000073.7:g.15680387C>A | variant | SNP
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NC_000073.7:g.15680408C>G | variant | SNP
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NC_000073.7:g.15680186A>G | variant | SNP
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NC_000073.7:g.15680215G>A | variant | SNP
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NC_000073.7:g.15680261G>A | variant | SNP
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NC_000073.7:g.15680208C>T | variant | SNP
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NC_000073.7:g.15680209T>A | variant | SNP
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NC_000073.7:g.15680263C>G | variant | SNP
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