| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346704406 | snp | A/T | | | missense | VIM2 | TAIR10 | 1:24589596 | GCGGTGCCAGGTGAA[A/T]CCTCCGTCAGAAGAG | 842919 |
| rs346768975 | snp | C/T | | | synonymous-codon | VIM2 | TAIR10 | 1:24589932 | TTGTTCTATTTGCAT[C/T]CAATTGCCAGAGAGA | 842919 |
| rs346788799 | snp | A/G | | | synonymous-codon | VIM2 | TAIR10 | 1:24589944 | CATTCAATTGCCAGA[A/G]AGACCTGTTACGGTT | 842919 |
| rs347135406 | snp | A/C | | | intron-variant | VIM2 | TAIR10 | 1:24589960 | AGACCTGTTACGGTT[A/C]GTTTTCACTCGCTAA | 842919 |
| rs347376343 | snp | A/T | | | intron-variant | VIM2 | TAIR10 | 1:24590145 | GCTTGTGATGTGTTA[A/T]GTACTTGTTAGATCT | 842919 |