Search Result
Gene id | 101927609 | ||||||||||||||||
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Gene Summary SNPs Diseases PubMed | |||||||||||||||||
Gene Summary |
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Gene Symbol | LOC101927609 Gene UCSC Ensembl | ||||||||||||||||
Gene location |
7p21.1 (17298537: 17133915) Exons: 12 NC_000007.14 |
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OMIM | 0 | ||||||||||||||||
SNPs |
rs10250822 Strand: Allele origin: Allele change: Mutation type: snv NC_000007.14 g.17293365C>A NC_000007.14 g.17293365C>G NC_000007.14 g.17293365C>T NC_000007.13 g.17332989C>A NC_000007.13 g.17332989C>G NC_000007.13 g.17332989C>T|SEQ=[C/A/G/T]|GENE=LOC101927609 rs10247158 Strand: Allele origin: Allele change: Mutation type: snv NC_000007.14 g.17285544A>T NC_000007.13 g.17325168A>T|SEQ=[A/T]|GENE=LOC101927609 rs10249788 Strand: Allele origin: Allele change: Mutation type: snv NC_000007.14 g.17298523C>G NC_000007.14 g.17298523C>T NC_000007.13 g.17338147C>G NC_000007.13 g.17338147C>T XR_927073.2 n.16G>C XR_927073.2 n.16G>A|SEQ=[C/G/T]|GENE=AHR LOC101927609 101927609 rs3757824 Strand: Allele origin: Allele change: Mutation type: snv NC_000007.14 g.17296411T>C NC_000007.14 g.17296411T>G NC_000007.13 g.17336035T>C NC_000007.13 g.17336035T>G|SEQ=[T/C/G]|GENE=LOC101927609 |
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Diseases
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PubMed references
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