| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs13466800 | snp | C/T | | | synonymous-codon | Rnf187 | Mm_Celera | 11:58938784 | CCGCCGCCCGCAGCC[C/T]TGGCGCTCCCCGCGG | 108660 |
| rs13466801 | snp | C/T | | | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58938647 | CGAGGAGGACGGGCC[C/T]TTCCCGTGCCCGGAG | 108660 |
| rs13466802 | snp | A/G | | | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58933054 | ACCACTTGGCAGCTC[A/G]GAAGCCCCTGCTTCT | 108660 |
| rs13466803 | snp | C/T | | | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58938494 | GCTGCAGCTGCTCTG[C/T]CGCGCCGACGGGGAT | 108660 |
| rs13466804 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58934069 | CGCTTCCGGTCCCTG[C/T]TGCAGGCTGTGTCAG | 108660 |
| rs13466805 | snp | A/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933069 | CCAGCCCTGCCTGGG[A/T]CCACTTGGCAGCTCG | 108660 |
| rs13466806 | snp | C/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58932676 | ATCCCCAAAGTGATT[C/T]CTCCTCCTTCCCACC | 108660 |
| rs13466807 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932836 | GGGTTTGGCTGGGAC[C/T]TGAGTGTTAATGCAG | 108660 |
| rs13466808 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932958 | TTCCCATTGGTGCCC[A/G]TGACAGGGTTGGCTC | 108660 |
| rs26971820 | snp | G/T | 0.5 | 0 | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58934034 | GCTGAGGCCCAGGTT[G/T]CGGTGCTTCTTCTCC | 108660 |
| rs26971821 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf187 | Mm_Celera | 11:58933527 | ACAGAGCCAAGGTGA[C/T]TTGACAACCCATCTA | 108660 |
| rs26971822 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf187 | Mm_Celera | 11:58933500 | AGTGCTGCTATCCTG[A/C]GTACAATGCACACAG | 108660 |
| rs29386458 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936773 | TAAAAGGGACTCCCA[A/C]AGAGCCCCCTCCCCA | 108660 |
| rs29388353 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932896 | ACTAACACACACAGG[C/T]TGACTGTAACTGGTG | 108660 |
| rs29394203 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940221 | TAAATAAATAAATAA[A/T]TAAATAAAAGTGTGT | 108660 |
| rs29394747 | snp | A/G | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935856 | ACCAGACACACTCTC[A/G]TTTCTGAGTACATTT | 108660 |
| rs29397346 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939145 | CCAAACCCAGATCCT[C/T]ACAAAGATACTCCCT | 108660 |
| rs29402991 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939612 | GTGTGTCACTGTGGC[C/T]GTGGGCTTTGAGACC | 108660 |
| rs29406824 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937435 | GGATTTTAGGTAGGT[C/T]CCCTTTAGTGTCAGC | 108660 |
| rs29409297 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935836 | GCTGGACAAGCACTG[C/T]ACCAACCAGACACAC | 108660 |
| rs29410563 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939316 | GCAGGATAAAACTGG[C/T]TAGGTAGGCAGATGC | 108660 |
| rs29412533 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940213 | TAAATAAATAAATAA[A/T]TAAATAAATAAATAA | 108660 |
| rs29414988 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939883 | GCTCCAAACACTATG[A/G]CAGCAGCCACATCTG | 108660 |
| rs29416275 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937556 | GGACAACCCCAGCAG[C/T]ATGTTCTGACAGAGT | 108660 |
| rs29421098 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935789 | TGTCTGTGGTGCTTG[C/T]TTTGCACGATTACAT | 108660 |
| rs29421151 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936899 | AATCATGTGTGTGGT[A/T]TTGTGTGGCAGCCAG | 108660 |
| rs29433997 | snp | A/G | 0.5 | 0 | intron-variant | Rnf187 | Mm_Celera | 11:58936235 | TGCCAGCCAGATAAC[A/G]GCTGTCTGGCCAAGC | 108660 |
| rs29434418 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936822 | AGTGAGAAAGGCCAC[A/C]GGAAGCTAGCCCCAA | 108660 |
| rs29438000 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939787 | GCCCCAGTTAAATGT[C/T]CTTTATAAGAGTTAC | 108660 |
| rs29440469 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939463 | ATTGTGTTAATACAG[C/G]TGTAGTCAGCTATCT | 108660 |
| rs29442033 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936924 | AGCCAGAAAACAGAA[G/T]GTTCTACTGGTAACA | 108660 |
| rs29442154 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf187 | Mm_Celera | 11:58936649 | CTAGCTAAGTACCAA[A/C]TCTGTGTGTCCCCAA | 108660 |
| rs29445525 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf187 | Mm_Celera | 11:58936107 | ACCTTGACAGCAGGA[C/T]TGGAAACAGACACTC | 108660 |
| rs29447736 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf187 | Mm_Celera | 11:58937342 | GAAAGTGGTTGTTTC[G/T]TAAAAGGGTCTCCTG | 108660 |
| rs29449002 | snp | A/G | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58938179 | AATAGCTCGAGGGAC[A/G]TAGCAGGGTCCGGGA | 108660 |
| rs29451560 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf187 | Mm_Celera | 11:58936268 | CCTCTGACTACAGGA[C/T]CCCCATCTTCGTATT | 108660 |
| rs29455279 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937514 | TTTGTGGAGATTGCT[C/G]TCTTAGTAAGGGGAC | 108660 |
| rs29462159 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937593 | ACCTCAGTTTGGGAC[C/T]TGGATGTAACCACAG | 108660 |
| rs29468395 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936086 | AGCAACACTTCTAGC[A/G]GCCTAACCTTGACAG | 108660 |
| rs29471820 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937048 | AGAGAGGAGCCCTAC[A/G]GACACTCAACTCACC | 108660 |
| rs29474736 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935664 | CCCCTGTGCTGCAGG[C/T]CCTCTCCACTGGATA | 108660 |
| rs29480356 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf187 | Mm_Celera | 11:58936487 | GGGAACTATAATGAA[C/T]TTTAATATATAAAAG | 108660 |
| rs29484551 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932335 | AACCCAGCCCACCTG[C/T]GAGTCAAGTTGAGGC | 108660 |
| rs29486311 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940217 | TAAATAAATAAATAA[A/T]TAAATAAATAAAAGT | 108660 |
| rs29487085 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939804 | TTTATAAGAGTTACA[C/T]TGGTCATGGTGTCTC | 108660 |
| rs33849103 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940276 | GAAAGAGAATTGTGT[A/G]TGTGTGTGTGTGTGT | 108660 |
| rs45760476 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935239 | CTATGAAACGGCACA[A/G]CATTAACACAGATGC | 108660 |
| rs45948376 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940009 | TCTAGGAAAAAAATA[C/T]TACATAGAAAGATGC | 108660 |
| rs45982749 | snp | G/T | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940893 | AGCTTTAAGATTAGT[G/T]GCCCTTATCAGAATT | 108660 |
| rs46013744 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935646 | CAGAGCCACCTGCAT[C/T]CCCCCCTGTGCTGCA | 108660 |
| rs46076054 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935667 | CTGTGCTGCAGGTCC[A/T]CTCCACTGGATACAA | 108660 |
| rs46693454 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933730 | GGATGAGGGATGACA[G/T]GGGGGATACCCTGGC | 108660 |
| rs46713005 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935305 | TCTAACACAGAGCCA[C/T]CTGCATCCTCTCCTT | 108660 |
| rs46821867 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940018 | AAAATATTACATAGA[A/G]AGATGCATGTAAATA | 108660 |
| rs46822979 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935431 | CCTGTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs46838563 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933602 | ACAGCTGATGGGTAT[A/G]TGGGAAGGGAATACC | 108660 |
| rs46908253 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935399 | TCTAACACAGAGCCA[C/T]CTGCATCCTCTCCTT | 108660 |
| rs47036666 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934374 | AATTAAATCTACTTT[A/T]AAAACTAAAATCACA | 108660 |
| rs47037929 | snp | C/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933211 | TATGTGCATGGCCAG[C/T]GGGGCACCTCTGATG | 108660 |
| rs47043427 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934632 | ACCACCTTGGGTGCA[A/T]TCACTAGACACAGTA | 108660 |
| rs47169723 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933743 | CAGGGGGGATACCCT[A/G]GCTACTCCTGCTCAC | 108660 |
| rs47449036 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934949 | TCGAACTCAGAAATC[C/T]TCCTGCCTCTGCCTC | 108660 |
| rs47604724 | snp | A/C | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940011 | TAGGAAAAAAATATT[A/C]CATAGAAAGATGCAT | 108660 |
| rs47778021 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934643 | TGCATTCACTAGACA[C/T]AGTAGGCAGAGCCTT | 108660 |
| rs47982461 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933665 | AAGCTCAGGCTGACT[G/T]CCAAGCAGGTTGCCT | 108660 |
| rs48899298 | snp | A/G | | | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932645 | TTCTGCAGGGAAGGA[A/G]GTCCCTTCCATCAGA | 108660 |
| rs49285351 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935383 | TCCCTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs49330478 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933597 | CCCAAACAGCTGATG[A/G]GTATGTGGGAAGGGA | 108660 |
| rs49485933 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934572 | TGGATGTTGGTCTCA[C/T]GGGCCACCAGCTGGC | 108660 |
| rs49740425 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934837 | CTTCCCAAATGAATC[C/T]TTTTTTTTTTTTTTT | 108660 |
| rs49778455 | snp | C/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940537 | TACTGAGGTCTGGCG[C/G]TCAAACCCAGGGCAT | 108660 |
| rs50012016 | snp | A/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58933725 | GATGAGGATGAGGGA[A/T]GACAGGGGGGATACC | 108660 |
| rs50034408 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934352 | TCAAAATAAGCTGGG[A/T]CTTTTGAATTAAATC | 108660 |
| rs50123141 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58933705 | GTCCAAGACTCGGGG[A/C]ATGAGATGAGGATGA | 108660 |
| rs50194099 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934466 | TCTGACATCCCTTAT[A/G]GTGGTATTAGCTTGG | 108660 |
| rs50723312 | snp | A/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933023 | ATGCCACACTAAGCT[A/G]AGCCATGGCAAAACA | 108660 |
| rs51022380 | snp | A/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940732 | AAGGATGAAGGACAC[A/G]TGGGAAGATACGATG | 108660 |
| rs51101069 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933579 | CTCTGAGGTTGTATA[A/G]GCCCCAAACAGCTGA | 108660 |
| rs51144340 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58935289 | CCTGTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs51244561 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934366 | GACTTTTGAATTAAA[C/T]CTACTTTAAAAACTA | 108660 |
| rs51276665 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933476 | ACACAGGTATAGACA[A/G]TAAGACAGAGTGCTG | 108660 |
| rs51542884 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934521 | GCAGGGCCTTGCAGC[G/T]CTCCATCACTCATGT | 108660 |
| rs51583444 | snp | C/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934935 | AGACCAGGCTGGCTT[C/G]GAACTCAGAAATCCT | 108660 |
| rs51724166 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934476 | CTTATGGTGGTATTA[A/G]CTTGGTCCCACTGTC | 108660 |
| rs51766213 | snp | A/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940719 | ATGGATGGGAAGCAA[A/G]GATGAAGGACACGTG | 108660 |
| rs52027959 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934451 | ACATGAAAGGATGCC[C/T]CTGACATCCCTTATG | 108660 |
| rs52629277 | snp | C/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934878 | GTTTTTTTGAGACAG[C/G]GTTTCTCTGTGTAGC | 108660 |
| rs52644463 | snp | A/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940189 | CTGTCTCAAAAATAA[A/T]TAAATAAATAAATAA | 108660 |
| rs211908727 | in-del | -/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934308 | TTAAAGAAAGAGAAG[-/C]GCCCTCTACTCTGAA | 108660 |
| rs211946459 | in-del | -/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935314 | GAGCCATCTGCATCC[-/T]CTCCTTCCCTGTGTT | 108660 |
| rs212309403 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936238 | CAGCCAGATAACAGC[C/T]GTCTGGCCAAGCTCC | 108660 |
| rs212690664 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937128 | TCCCCATATCCAGGA[G/T]AGCCCACTTACCTTC | 108660 |
| rs213043928 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934950 | CGAACTCAGAAATCC[G/T]CCTGCCTCTGCCTCC | 108660 |
| rs214047589 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58936205 | GGAAGAATGTTTTTG[A/C]TGAAAGGACATAAAT | 108660 |
| rs214088811 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940148 | CACAGTGAGTTTCAG[G/T]CCAATCAAAGCTATA | 108660 |
| rs214092284 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939084 | CTTCCACACTGGTTC[C/T]CGTAGCAGCTCACGA | 108660 |
| rs214404009 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58938009 | GCTTGCACCGATGAA[A/G]TCACACCGGGATAGG | 108660 |
| rs214430100 | in-del | -/AAATAAATAAATAAATAAAT | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940183 | AAGACCCTGTCTCAA[-/AAATAAATAAATAAATAAAT]AAATAAATAAATAAA | 108660 |
| rs214478796 | in-del | -/CT | | | intron-variant | Rnf187 | Mm_Celera | 11:58933948 | TCTCTTCCACCGTGG[-/CT]CTGAGTTGACTAGAG | 108660 |
| rs214756284 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58935228 | TCAAGATCCTTCTAT[A/G]AAACGGCACAACATT | 108660 |