RSID | rs183712207 |
HGVS | NC_000002.11:g.196611282G>A |
Chromosome | 2 |
Start position | 196611282 |
Stop position | 196611282 |
Associated gene(s) | DNAH7, SLC39A16, LOC107985972 |
Mutation type | Tagged SNP |
Reference | G |
Alternative | A |
Associated allele | A |
Associated African Allele Frequency | 0.0045 |
Consequence | Intronic |
Other population frequencies link | ALFA rs183712207 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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