RSID | rs3787950 |
HGVS | NC_000021.8:g.42866296T>C |
Chromosome | 21 |
Start position | 41494369 |
Stop position | 41494369 |
Associated gene(s) | TMPRSS2 |
Mutation type | SNP |
Reference | T |
Alternative | C |
Associated allele | C |
Associated African Allele Frequency | 0.2018 |
Consequence | Synonymous variant |
Other population frequencies link | ALFA rs3787950 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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