| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193335586 | snp | G/T | 0.490001 | 0.0699965 | intron-variant, utr-variant-5-prime | cdk-5, kel-3 | WS195 | III:13464798 | TTCTGCAAATACTTC[G/T]AGTTTGAGTAAGTAT | 176775 |
| rs193335587 | snp | A/G | 0.04875 | 0.148319 | intron-variant, synonymous-codon | kel-3, cdk-5 | WS195 | III:13464882 | ATTAGGTACGATTTG[A/G]CTCCATGTAAGCGTT | 176775 |
| rs193335588 | snp | A/T | 0.0296962 | 0.118179 | intron-variant | cdk-5, kel-3 | WS195 | III:13465032 | AAATCTACTCAATAC[A/T]CTGTTCTCTGTCCTG | 176775 |
| rs193335589 | snp | A/C | 0.0198 | 0.0975088 | missense | kel-3 | WS195 | III:13470318 | GGAGCTGCCACGTTC[A/C]AAGGAAAAATCTACG | 176775 |
| rs193603081 | snp | A/G | | | synonymous-codon | kel-3 | WS195 | III:13466626 | CGATGTGGCCTTGTT[A/G]GTTGAAAATCGAAAG | 176775 |
| rs193603082 | snp | C/T | | | intron-variant | kel-3 | WS195 | III:13469408 | TTTTTTTTTATTTTT[C/T]GTTTTTTTTTCTTTT | 176775 |
| rs193603083 | snp | C/T | | | intron-variant | kel-3 | WS195 | III:13469448 | TGAATCGGAAATTTT[C/T]GATTTTGCGGAAAAT | 176775 |
| rs353122231 | snp | C/T | | | intron-variant | kel-3 | WS195 | III:13467241 | CTTTAAAGAGAATTT[C/T]TGATTTTCAAGATCT | 176775 |
| rs353149825 | snp | A/T | | | intron-variant | cdk-5, kel-3 | WS195 | III:13465495 | GCAAATTTAATTTTT[A/T]AAAAAAACCTGCAAA | 176775 |
| rs353159004 | snp | A/G | | | intron-variant | kel-3 | WS195 | III:13468719 | AAACAAATATTAATG[A/G]TTCCGTGATTATTTT | 176775 |
| rs353172549 | snp | A/T | | | intron-variant | kel-3 | WS195 | III:13469384 | AAATTGACAGAAAAA[A/T]TTTTTTTATTTTTTT | 176775 |
| rs353174377 | snp | C/T | | | intron-variant, synonymous-codon | kel-3, cdk-5 | WS195 | III:13465637 | TGGGACGCCAAACGC[C/T]CTGGCTAATCCAAAA | 176775 |