| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs64192302 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259818 | AATGGATTTGGGGGA[A/G]AAAAATTGAGTATAG | 29534 |
| rs64834919 | snp | A/C | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259703 | ATTAATTGAACCTCN[A/C]ATTATATTTATTTCA | 29534 |
| rs65018245 | snp | G/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259809 | TGGGGATGGAATGGA[G/T]TTGGGGGAAAAAAAT | 29534 |
| rs65124082 | snp | G/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259824 | TTTGGGGGAAAAAAA[G/T]TGAGTATAGTATTTT | 29534 |
| rs65967354 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259804 | GGGGTTGGGGATGGA[A/G]TGGATTTGGGGGAAA | 29534 |
| rs66219705 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259783 | GATCTGTGCCTGCCA[A/G]AAAAGGGGGTTGGGG | 29534 |
| rs104904441 | snp | C/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98267789 | AGAAGGAAAGAAAGA[C/G]AGCTTCCAGTTAAGA | 29534 |
| rs105176293 | snp | C/T | 0 | 0 | upstream-variant-2KB | Pex2 | Rn_Celera | 2:98250321 | TGAGCAAAAGGGCCA[C/T]AGTCCTCCACTGAGC | 29534 |
| rs105424793 | snp | A/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259533 | AGACTACTTCCATTA[A/T]GTTGAAATGATTTTA | 29534 |
| rs105445001 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98260435 | GTCTTCCTCCTGGCT[C/T]ACATAAGCACATCTA | 29534 |
| rs105628765 | snp | C/T | 0 | 0 | downstream-variant-500B | Pex2 | Rn_Celera | 2:98269530 | GGTCTTCTGAACTAA[C/T]AATATAAGAATTCAT | 29534 |
| rs106107507 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98261236 | TTAAGTATTGGATCC[A/G]TTAGACTCTGCTAAG | 29534 |
| rs106292857 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98261917 | AGATCAAGAGATCGA[A/G]ATCATATTGGGAAAA | 29534 |
| rs106417432 | snp | C/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98263246 | GAGTGAGATATCTCT[C/G]GGATGAACTAGAAAC | 29534 |
| rs106478028 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98257993 | CTATGGTTTTTCAGT[A/G]TATGTAGAAAATAAA | 29534 |
| rs106478265 | snp | C/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98254550 | TCATTTGATTATTCT[C/G]GCACCCCAAAGTTAT | 29534 |
| rs106533496 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98263010 | ACTGGATATTAGCCA[C/T]AAAGGATTCCACACT | 29534 |
| rs106770544 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98266745 | ATATGGAATAAATAA[C/T]ATGATGACCTCATAT | 29534 |
| rs106952039 | snp | C/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98263131 | CAGAAGTTGATGGAG[C/G]GGGGAGACTATACAA | 29534 |
| rs107061165 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Pex2 | Rn_Celera | 2:98252744 | CTGTCCAGCGGCCCG[C/T]AGCGGCGTCCGAGGG | 29534 |
| rs107315086 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98264071 | ACTAGGAGGAGAAAA[A/G]GGGGAAGCTGGTATC | 29534 |
| rs107403482 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Pex2 | Rn_Celera | 2:98252049 | GTGGTTATACAGGAT[A/G]CATCTCTAGACATCT | 29534 |
| rs107433461 | snp | C/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98262676 | AAACACTTTGGTAAT[C/G]GATTTGGTGGTTTCT | 29534 |
| rs107494644 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98260212 | TGTCTGGATGCTTTT[A/G]TGTTCCTGCTGTGAT | 29534 |
| rs107570568 | snp | A/G | 0 | 0 | downstream-variant-500B | Pex2 | Rn_Celera | 2:98269215 | TATTTTCAGGATAAA[A/G]GAACATTATAAGCTG | 29534 |
| rs107585836 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Pex2 | Rn_Celera | 2:98251479 | TTCCCTTATGAGTAT[C/T]TAGGAACCAATTTGT | 29534 |
| rs197133426 | snp | G/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98261328 | GTCTCTAGAAAGAAG[G/T]GTTTTGAAAAAGGTT | 29534 |
| rs197367194 | snp | A/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98264649 | CTGCTCACCTTAGAT[A/T]CTCTCTCTCTCTCTC | 29534 |
| rs197438950 | snp | C/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | Pex2 | Rn_Celera | 2:98252938 | CTTCCATCGTCCCTT[C/T]GGTTCCTCGGCTCCT | 29534 |
| rs197444979 | snp | G/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98256316 | TGTTTTTGTTTTCCA[G/T]GACTGTCCCTTTATT | 29534 |
| rs197464019 | snp | A/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98266222 | CTTAACATTTAACAT[A/T]TGCCTTTTTTAAAAA | 29534 |
| rs197727842 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98267645 | CTCCTATCCCTCCCT[C/T]TCTCTCTCTCTCTCT | 29534 |
| rs197990681 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Pex2 | Rn_Celera | 2:98251344 | TAGTTATTATTGTGT[A/G]TGCACATGTGGTGTG | 29534 |
| rs198310567 | snp | C/T | 0 | 0 | missense | Pex2 | Rn_Celera | 2:98268462 | CGCCTCCTTGGCATT[C/T]ATTCTGTATTTTGCA | 29534 |
| rs198390122 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98256331 | TGACTGTCCCTTTAT[C/T]ATATATCCTGCTATA | 29534 |
| rs198610197 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98254532 | TTTGTTTTCAGTCTG[C/T]GTTCATTTGATTATT | 29534 |
| rs198625373 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Pex2 | Rn_Celera | 2:98251145 | TATATTAATAAATCC[A/G]GAAATTATTTTAAAT | 29534 |
| rs198655555 | snp | C/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98266554 | TTTCAGATCACATGA[C/G]CCACTGGCAAAAGTT | 29534 |
| rs198743499 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98264650 | TGCTCACCTTAGATT[C/T]TCTCTCTCTCTCTCT | 29534 |
| rs198879533 | snp | A/G | 0 | 0 | downstream-variant-500B | Pex2 | Rn_Celera | 2:98269288 | CTCGCTTGTAACTAA[A/G]CTTTTCCCTGAAGCC | 29534 |
| rs198952873 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98266859 | GTGTGTTTGAAGACA[A/G]TCCTAGCCAAATTTA | 29534 |
| rs199037679 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98259974 | CTTAACCATATCGAT[A/G]GGGTTAAATTGCCAA | 29534 |
| rs199276073 | snp | A/G | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98265723 | ATGAATGCATGAGGG[A/G]AAAAGTACACAGAAC | 29534 |
| rs199364965 | snp | C/T | 0 | 0 | intron-variant | Pex2 | Rn_Celera | 2:98254703 | TTCTTGTTTTTCTTT[C/T]TTTTTTTTTTTTTTG | 29534 |