| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193334256 | snp | A/G | 0.0599426 | 0.162414 | intron-variant | cor-1 | WS195 | III:10253915 | AACGCCACGGCCTAG[A/G]AATCGAATTCTAGGC | 176440 |
| rs193334257 | snp | A/G | 0.428728 | 0.174804 | intron-variant | cor-1 | WS195 | III:10253944 | GCCATGAAAAGCCCC[A/G]CCGTAGCCTAGGATT | 176440 |
| rs193334258 | snp | A/G | 0.433715 | 0.169555 | intron-variant | cor-1 | WS195 | III:10253949 | GAAAAGCCCCACCGT[A/G]GCCTAGGATTTTCCC | 176440 |
| rs193334259 | snp | A/C | 0.474802 | 0.10938 | intron-variant | cor-1 | WS195 | III:10253988 | AATGTACATTCTAAT[A/C]TGTTGTTATTGTTTT | 176440 |
| rs353109688 | snp | A/G | | | intron-variant | cor-1 | WS195 | III:10253280 | GAACTAAATTATTTA[A/G]AAAAAAACTAATGCT | 176440 |
| rs353117242 | in-del | -/A | | | intron-variant | cor-1 | WS195 | III:10250065 | AGATCAATAATTTTT[-/A]AAAAAAAAGTTAACT | 176440 |
| rs353137737 | in-del | -/T | | | intron-variant | cor-1 | WS195 | III:10249940 | TTTCCGGATTTTTAA[-/T]TTTTTTAATTATTTT | 176440 |
| rs353146398 | snp | G/T | | | intron-variant | cor-1 | WS195 | III:10249193 | AGCGGATTTTACTAC[G/T]TAGCCGCAAAAAAAT | 176440 |
| rs353162555 | in-del | -/T | | | intron-variant | cor-1 | WS195 | III:10252363 | TTCTTTAATATCAAA[-/T]TTTTTTAAAATTCCA | 176440 |
| rs353171348 | snp | C/T | | | intron-variant | cor-1 | WS195 | III:10252351 | TTGAAAATTCTTTTT[C/T]TTTAATATCAAATTT | 176440 |