RSID | rs334 |
HGVS | NC_000011.9:g.5248232T>A |
Chromosome | 11 |
Start position | 5248232 |
Stop position | 5248232 |
Associated gene(s) | HBB |
Mutation type | Tagged SNP |
Reference | T |
Alternative | A/C/G |
Associated allele | A |
Associated African Allele Frequency | 0.003 |
Consequence | Missense Variant |
Other population frequencies link | ALFA rs334 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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