| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs29327510 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Pex7 | Mm_Celera | 10:19903821 | TTTGGTATTTCCAAA[A/G]TATAAACTAGTTCCT | 18634 |
| rs45657950 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pex7 | Mm_Celera | 10:19876075 | TACAATGTTCAAGGT[A/G]AAACATTATAAAAAT | 18634 |
| rs45684514 | snp | A/C | | | intron-variant | Pex7 | Mm_Celera | 10:19892088 | TTGGTACACACACCA[A/C]GCCTTATGAGCAGCT | 18634 |
| rs45718972 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Pex7 | Mm_Celera | 10:19862162 | GATAGTAAGAAAGAA[A/C]TTGGTAACACATTTA | 18634 |
| rs45741110 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19891802 | TCAGGTTTGAAACCA[G/T]CCCTATGAAACCACA | 18634 |
| rs45770751 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19884758 | GTTGCACACAGGATG[A/T]ATTAGAGAGGTCTCT | 18634 |
| rs45789949 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19880448 | AAGAACATCTGGGGG[A/G]CTACTTCATTGAACC | 18634 |
| rs45810956 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pex7 | Mm_Celera | 10:19861369 | CACGTGGCCATAATA[C/T]TTGGAGAGACCTGGA | 18634 |
| rs45822134 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19881082 | TTCAATTACTCTCTA[C/T]CTGTGTTGATGACTG | 18634 |
| rs45857641 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19874807 | ACGCAATGAAATACA[A/G]TGTTAGCTCCTTCTT | 18634 |
| rs45876223 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19887025 | ACCGACTACTGGTTA[C/T]GTTTTCACTCTGTAT | 18634 |
| rs45924836 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pex7 | Mm_Celera | 10:19881938 | AGGGAATATGCTGAG[A/C]CCTGTGATGCTAACA | 18634 |
| rs45949726 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19881535 | CTATCGGCTGAGTTG[C/T]TACTACCAAAGGCCA | 18634 |
| rs45982950 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Pex7 | Mm_Celera | 10:19874728 | CAGAGGTAAAGTAAC[A/G/T]CGCTATTATTTCATG | 18634 |
| rs45988396 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Pex7 | Mm_Celera | 10:19865305 | CAGAGCAGGGAGACC[A/C]ACAGTTCCGCATTTG | 18634 |
| rs46009554 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Pex7 | Mm_Celera | 10:19899810 | AAATGGTTGATTGCA[A/C]CTTAACATGCAAAAG | 18634 |
| rs46026217 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19883626 | TACTAAAATATCACA[C/T]ATCCTCAGTTTCAGA | 18634 |
| rs46034186 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19874651 | ACAAATGAGAACTTA[C/T]TCACACTCTTTTGAC | 18634 |
| rs46070623 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19890033 | TGAGCATCACTTCCC[A/G]TTCTGAAGTATGCTC | 18634 |
| rs46091121 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pex7 | Mm_Celera | 10:19901921 | GTGGACGTAGAGCTC[A/G]GGATTATTTGGTCTT | 18634 |
| rs46102161 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pex7 | Mm_Celera | 10:19865685 | GCATGGGCTAGACCA[C/T]TTACAGCACAGTTGT | 18634 |
| rs46104051 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19903407 | GGTGATGTAGCAACT[A/G]AAGGTAACTTAAAGG | 18634 |
| rs46136610 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19900850 | CAGAGAAGAATCTGA[C/G]TCCTGCTTTGATGTT | 18634 |
| rs46139849 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19895241 | GAAAACAGTGCTGCT[C/T]CATCCGACCTCTTGG | 18634 |
| rs46142418 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19888277 | TGCACTGTTGAACTT[G/T]TAAGAATATCTGTTC | 18634 |
| rs46160974 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19877960 | CGTGTCAGGCTGCGG[A/G]CTACACGTGCACTTG | 18634 |
| rs46176180 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19895974 | TGACCAAGACAGACA[C/T]GAAATCCAAAAAAGT | 18634 |
| rs46226249 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Pex7 | Mm_Celera | 10:19883871 | CCTGCTTTTGGTGGC[C/G]TGCACCATCTGCCTG | 18634 |
| rs46227003 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19877223 | GTTTACACACACATG[A/C]ACATGCAGGCGCACA | 18634 |
| rs46240320 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19892359 | GTTACTTGCCTAGTA[A/G]GTGTGCTGCCATGAT | 18634 |
| rs46253113 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pex7 | Mm_Celera | 10:19901584 | AAATGTGTCTAAATA[C/T]ATATTTTTCACTTAT | 18634 |
| rs46282725 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19881707 | AAAAGAGAGCATATT[A/G]ATCTTTCTAATAAAA | 18634 |
| rs46322268 | snp | C/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19898377 | CAAGGGTCTGCTCAC[C/G]GGCAGCACTGTGTCC | 18634 |
| rs46332387 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19886344 | CTGTTAATGTAGAGA[A/C]CTGATAATCAGGAGA | 18634 |
| rs46358067 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19886719 | AACATCAAGTAGTGA[A/C]TTTTTATATCATTCC | 18634 |
| rs46390223 | snp | A/G | | | intron-variant | Pex7 | Mm_Celera | 10:19872567 | TATGAGCGCCCCAAC[A/G]AGAGCTATGAGCGCC | 18634 |
| rs46402967 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19887803 | AGTTAAGTTTTGTTC[A/G]GTTTTCTAAGCCTAA | 18634 |
| rs46430231 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19875855 | CAACGAGGTAAAAGT[C/T]ATCCATACTTATCAG | 18634 |
| rs46438947 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pex7 | Mm_Celera | 10:19901700 | GCTGCATCCGAAGCA[C/T]GCCTTGTTCACCTCG | 18634 |
| rs46481616 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19889741 | TAGCTCTCAGCCAAA[A/G]GTGAACGCTCAGTTG | 18634 |
| rs46498880 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pex7 | Mm_Celera | 10:19866556 | TGTGTGGATATATGA[C/T]TGTAGGTACACATGG | 18634 |
| rs46506910 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19869648 | TCATTTTGATAGCTT[A/G]TAAAATGGAAGTTTA | 18634 |
| rs46515167 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19902246 | GTAGGCAGCCAATGG[A/G]CTTTCTTGGATTACC | 18634 |
| rs46528334 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Pex7 | Mm_Celera | 10:19878546 | AACAGCAATTTCTCT[A/T]TAGAAACAGTTTCTC | 18634 |
| rs46539434 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pex7 | Mm_Celera | 10:19864491 | GCCATCAACAATGGA[A/G]AGCATGGCAAACTTT | 18634 |
| rs46548684 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19900654 | CCAGTCACACAGCGC[C/T]GCGCCAAGTCCTGAA | 18634 |
| rs46571678 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19886632 | ATTCCCTAAATATAA[A/G]CTAACACACTTAGAA | 18634 |
| rs46572923 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Pex7 | Mm_Celera | 10:19865399 | CTAAAGTTACATATG[C/T]GACAAAAGGAAAAAT | 18634 |
| rs46580278 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19902472 | ACTAAAGCCAAAGCA[C/T]CCTGATGCAGATGTT | 18634 |
| rs46608893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19896317 | CCTATACTTTTATGA[A/G]ATTGGTGGGTATAAA | 18634 |
| rs46621685 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19904535 | CAAAGAGATTTCAAA[C/T]AAACAATAAGGGAAG | 18634 |
| rs46634328 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19889994 | AATTACAAAGCAGGG[A/G]TAAGATCACCACAAA | 18634 |
| rs46639263 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Pex7 | Mm_Celera | 10:19861662 | GTGCCAACTACTAGG[C/T]AACATTCTACACAGA | 18634 |
| rs46705402 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19883269 | AGTTTCTACTCAAGC[G/T]TTATTAAATAATTAA | 18634 |
| rs46740921 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Pex7 | Mm_Celera | 10:19861502 | TATCCCATGGGCTAG[A/C]ACCAAAACTTCACAG | 18634 |
| rs46816167 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19871392 | TAGGAATCCGTCGGT[C/T]GGATGTGCTCAGTAT | 18634 |
| rs46847922 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19896708 | TCCTCTGGCTCTAAG[A/T]CCATGTACACTCTCA | 18634 |
| rs46920899 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pex7 | Mm_Celera | 10:19889115 | TCCAGCTCTTCCTTA[C/T]GGTTTTTATATTTAC | 18634 |
| rs46960200 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19869433 | AGAAAAAGAAAATAC[A/G]GTTGCTAAAACCCTT | 18634 |
| rs46967121 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19884722 | CTCAGCGAAGTTGCA[C/T]ACATACAAACACTAC | 18634 |
| rs46989827 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Pex7 | Mm_Celera | 10:19863038 | CCCACTCTCCCACCT[C/T]ACTCAGGACACAGCC | 18634 |
| rs46992252 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19878470 | CTCCATGTGAGCCAC[A/G]CACTGATGGGGTCCC | 18634 |
| rs47107044 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19873111 | ATGATTTTAAGAATT[A/G]AGCAGGAGCTAGTTT | 18634 |
| rs47109575 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19895249 | TGCTGCTCCATCCGA[C/T]CTCTTGGCAGGCAGC | 18634 |
| rs47122529 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19891059 | CCCTTCAAGTTGCAG[A/G]CCAACACTGACAGCA | 18634 |
| rs47148572 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19891430 | GTGCAAATATTCTTC[C/T]TCCCTGTGCCACATA | 18634 |
| rs47196177 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pex7 | Mm_Celera | 10:19861182 | TTTTGGGGACTGCTT[C/T]TACCTGACTGGAAGT | 18634 |
| rs47205290 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Pex7 | Mm_Celera | 10:19873935 | GATAACAGAAGCCAG[A/C]CGCACACAGAGAGAC | 18634 |
| rs47206988 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19890828 | ACCGACAGCACTGTT[G/T]TTCAGGGTTAGCACT | 18634 |
| rs47228970 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19894810 | CTATACACCTAAAAA[A/C]GTCAAGTCTTCATGT | 18634 |
| rs47239987 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19883963 | TTAGTGAACTCACTC[C/T]TGCACGCTTGATCAC | 18634 |
| rs47243233 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Pex7 | GRCm38.p3 | 10:19894323 | ACTCTCATGGCCCCT[A/G]AAGGTACACAGAGAA | 18634 |
| rs47253919 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Pex7 | Mm_Celera | 10:19864033 | ATATCAAAGAAAAAA[A/C]TGTCTTAAGTGCAGG | 18634 |
| rs47266036 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19903791 | CATCACATTCCTTAA[A/G]ACATATGCATGCATT | 18634 |
| rs47278287 | snp | G/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19900965 | GATTCCACCAAGACC[G/T]TCAATCCCAGAGCCT | 18634 |
| rs47303853 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19886183 | TGGAATTCCCAAAGA[A/G]GTCAAAGTTAAATCT | 18634 |
| rs47315793 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19863059 | GGACACAGCCACCGG[C/T]TAGAACGTAAGCTGC | 18634 |
| rs47326430 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19900602 | TGGAGTAAACAGCGC[C/T]GACTCTGTACCCGCC | 18634 |
| rs47330830 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19887873 | AAAAGAGTTCTGACA[A/G]TGTGGTATTCTTTTA | 18634 |
| rs47459929 | snp | A/C | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19903143 | CAGAATTTCCTAGAG[A/C]ATATAAAGAGACCAC | 18634 |
| rs47492552 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19902952 | TTGTCTTCAGCACAG[C/T]ACATATTCAAAGCTT | 18634 |
| rs47512643 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19873979 | ATGGACTCAGCCCCA[C/T]CTGTGCCTGAAAATT | 18634 |
| rs47547527 | snp | C/G | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19886397 | CACAGCACCACAGCA[C/G]AATCACCTGACAGGA | 18634 |
| rs47632723 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19896224 | TTTATGTGGGATCAA[A/T]ACTAAGTGCGTACTC | 18634 |
| rs47637373 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19891807 | TTTGAAACCATCCCT[A/T]TGAAACCACAGAATG | 18634 |
| rs47639296 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Pex7 | Mm_Celera | 10:19862271 | GACAGAGACTTTTGG[G/T]TAAGGTGAGACGCTG | 18634 |
| rs47642109 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pex7 | Mm_Celera | 10:19875799 | CTTACCACTTTTAGG[A/G]GAGCTTAGAGATAAA | 18634 |
| rs47688720 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19888893 | ATTCTCAAACCATCA[A/C]AATGCCTAAGAACTA | 18634 |
| rs47688782 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19889906 | CTTAAAACAGAGTTT[A/G]CCAAGCATACCATCT | 18634 |
| rs47690408 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19870843 | AGTCGGACCGGTCAA[C/G]GAGATTAATAAATAA | 18634 |
| rs47699538 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19892120 | TGCCACAGGAGGATG[A/T]AAACCACACTCAGGT | 18634 |
| rs47703668 | snp | A/C | 0.32 | 0.24 | intron-variant | Pex7 | Mm_Celera | 10:19900585 | AAGTGGAAATGAGAC[A/C]CTGGAGTAAACAGCG | 18634 |
| rs47741066 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19874795 | ATTATTAATAGAACG[C/T]AATGAAATACAATGT | 18634 |
| rs47751482 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19876788 | GGCTGACTGTTCCTT[A/G]GCTACACCACATGAA | 18634 |
| rs47780986 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pex7 | Mm_Celera | 10:19867577 | TGGCAAAATGTTATC[A/G]TTGCCAGTTGACTCT | 18634 |
| rs47847337 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Pex7 | Mm_Celera | 10:19878545 | AAACAGCAATTTCTC[C/T]TTAGAAACAGTTTCT | 18634 |
| rs47850893 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex7 | Mm_Celera | 10:19887998 | ATTAATACAATCAAT[C/T]TATTCCTGAATTCCT | 18634 |
| rs47864317 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex7 | Mm_Celera | 10:19890816 | TCTACTTCCTTGACC[A/G]ACAGCACTGTTGTTC | 18634 |
| rs47890478 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Pex7 | Mm_Celera | 10:19864499 | CAATGGAGAGCATGG[A/C]AAACTTTACTTAACT | 18634 |
| rs48008661 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Pex7 | Mm_Celera | 10:19862024 | TGGATTCAGCTTGAA[A/G]ACTATACTGAAAGTG | 18634 |