| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs193335636 | snp | C/G | 0.0298439 | 0.118454 | intron-variant | cul-2 | WS195 | III:13688877 | TAAAATTCAAACAAT[C/G]ATCTGAAAATGCTCC | 176806 |
| rs193335637 | snp | C/T | 0.00999975 | 0.0699991 | missense | cul-2 | WS195 | III:13690270 | ATGCTCGCAAATCGG[C/T]TTATAGCAAGCACAT | 176806 |
| rs193335638 | snp | G/T | 0.220641 | 0.24827 | missense | cul-2 | WS195 | III:13690611 | TCAGGAGTTTGAGAA[G/T]TTCTACACTGGGAAG | 176806 |
| rs193335639 | snp | C/T | 0.0103624 | 0.0712308 | intron-variant | cul-2 | WS195 | III:13691395 | AGCTATAAACTGTGG[C/T]CTAGAATTCTGAGAG | 176806 |
| rs193335640 | snp | A/G | 0.0198 | 0.0975088 | intron-variant | cul-2 | WS195 | III:13691410 | CCTAGAATTCTGAGA[A/G]ACTAGACGTATTTAG | 176806 |
| rs193603141 | snp | A/C | | | synonymous-codon | cul-2 | WS195 | III:13687218 | CGAGGTTCACCGTCC[A/C]CAGGCAAAACTGGCG | 176806 |
| rs193603142 | snp | C/T | | | synonymous-codon | cul-2 | WS195 | III:13688515 | CGTCTACGACATTTG[C/T]GTATCGATACCGACT | 176806 |
| rs193603143 | snp | A/C | | | intron-variant | cul-2 | WS195 | III:13691618 | TGTTGTTGGTCAAAA[A/C]CCTGTAAAACGAGAT | 176806 |
| rs193603144 | snp | C/T | | | intron-variant | cul-2 | WS195 | III:13691771 | TGGTCCGGAACCCCC[C/T]AAAAAAAAGCGAAAA | 176806 |
| rs353140670 | snp | A/G | | | intron-variant | cul-2 | WS195 | III:13689237 | TTAAGACCACAGTGC[A/G]CTTTTTCAAAATTTT | 176806 |
| rs353176237 | snp | A/G | | | intron-variant | cul-2 | WS195 | III:13691051 | GTTATGACTTTTTGA[A/G]TTCAAGCACTAAAAA | 176806 |
| rs353178699 | snp | A/C | | | intron-variant | cul-2 | WS195 | III:13688473 | TTTTTATAAATTTTT[A/C]ATTTTTTTAAATATT | 176806 |