| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs4221958 | snp | A/T | 0.21875 | 0.248039 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453424 | GTTGAAATTCAAATA[A/T]TAATATTTCTGATTT | 29864 |
| rs4221959 | snp | C/G | 0.21875 | 0.248039 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453282 | CCTCTTTCCCCACTG[C/G]CTGGAACCATAGCAA | 29864 |
| rs4221960 | snp | C/T | 0.394054 | 0.204324 | utr-variant-3-prime | Rnf11 | GRCm38.p3 | 4:109453244 | CTGCATCTCTTGTTA[C/T]TGTAGTGCTGAGGTT | 29864 |
| rs4221961 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453230 | ACTGTAGTGCTGAGG[A/G]TATTGAAGTTACAGA | 29864 |
| rs4221962 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Rnf11 | GRCm38.p3 | 4:109453201 | GAAACACATCTGGTG[C/T]GTTTCCTAGAAAAGT | 29864 |
| rs4221963 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453200 | AAACACATCTGGTGT[C/T]TTTCCTAGAAAAGTA | 29864 |
| rs4221964 | snp | A/C | 0.21875 | 0.248039 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453177 | GAAAAGTACCTGTTC[A/C]GTCTTGCTAGGTGAC | 29864 |
| rs6181743 | snp | A/G | 0.5 | 0 | intron-variant | Rnf11 | Mm_Celera | 4:109455611 | ctgggtagtctaaaa[A/G]ggcaagttgaagaca | 29864 |
| rs6183339 | snp | C/T | 0.5 | 0 | intron-variant | Rnf11 | Mm_Celera | 4:109455877 | GTCTTGTTGCTAGGC[C/T]TTTCCTACCATGACA | 29864 |
| rs13470786 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf11 | GRCm38.p3 | 4:109454215 | TTCAAGTGAACCATC[A/G]GTTTTGGTGGTTTTG | 29864 |
| rs28131907 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf11 | Mm_Celera | 4:109486179 | GCCTCTCTGCCTGTT[C/G]TGCATTTATTAATGG | 29864 |
| rs28131908 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB | Rnf11 | Mm_Celera | 4:109485207 | TGGTGTGCTTAAGGT[A/G]CAGCACCACCAACAA | 29864 |
| rs28131909 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf11 | Mm_Celera | 4:109485131 | AGCTTTGCAAACTCT[A/G]GTGATCTCCTCAGAA | 29864 |
| rs28131910 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf11 | Mm_Celera | 4:109485102 | CAAGAAAATTCAGAG[A/G]AGAGTTGAGAGGAAG | 29864 |
| rs28131911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109483821 | CTCAGGAGCCATGTC[A/G]CAGCTACAATTTGAA | 29864 |
| rs28131912 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109483820 | GCTCAGGAGCCATGT[C/T]GCAGCTACAATTTGA | 29864 |
| rs28131913 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf11 | Mm_Celera | 4:109483764 | AAACAGACAGTAGTC[C/T]GCGCTGAGTCTTAGG | 29864 |
| rs28131914 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109483100 | GTTGAGAAGATTCAT[A/C]AGTCATTATTTTTTT | 29864 |
| rs28131915 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109483035 | GCCTGCCACACTGAA[A/T]GAAAAACTTAGCCTG | 29864 |
| rs28131916 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109482791 | TTTCAGGTTGGAAAC[A/G]TCTGGGAGCAGGAAG | 29864 |
| rs28131917 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf11 | Mm_Celera | 4:109482660 | GAGCATGCTACCTCC[A/G]ATGGAGGGCACCTAC | 29864 |
| rs28131918 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf11 | Mm_Celera | 4:109481932 | TATTAAGTGAAAAAA[C/T]AAAACATTTAAGACT | 29864 |
| rs28131919 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf11 | Mm_Celera | 4:109481726 | TCAGGAAACTGGCGA[A/G]CTAGGACTCACAGCA | 29864 |
| rs28131920 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109481611 | ATGTGACTGAGCTAG[A/G]AATGAGTTTCAACTG | 29864 |
| rs28131921 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf11 | GRCm38.p3 | 4:109481174 | ATCTCCTATCTCAGC[A/G]GCCTCCACTTCCCAG | 29864 |
| rs28131922 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109481108 | AACACTACCCTCTAA[C/T]GTTGGTAAATACAAA | 29864 |
| rs28131923 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf11 | Mm_Celera | 4:109480884 | TCTACTTATGAAAGG[A/G]AGTTTAACTGGCTTG | 29864 |
| rs28131924 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109480457 | TGAAAATTCCTATCA[C/G]CTCCATGATGTCACA | 29864 |
| rs28131925 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf11 | Mm_Celera | 4:109479998 | AAGAATGAAAATATA[A/T]AAACGGAGTTGGAAG | 29864 |
| rs28131926 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf11 | Mm_Celera | 4:109468539 | CTGATAATTCTTTAA[A/G]CTGTAAGCGCTCCCA | 29864 |
| rs28131927 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Rnf11 | Mm_Celera | 4:109468221 | AAATAAACCTCAGGT[G/T]TTTGTTTTTCTTAGC | 29864 |
| rs28131928 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf11 | Mm_Celera | 4:109467943 | CTCCCAAATGTAAAA[G/T]AAATCAATAATGATC | 29864 |
| rs28131929 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf11 | Mm_Celera | 4:109466875 | AACATATGTCTACCA[C/T]ATGTCTAGGTATGGG | 29864 |
| rs28131930 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf11 | Mm_Celera | 4:109466291 | CATCAAACATGGCAA[A/C]AAACATACAAAGTAC | 29864 |
| rs28131931 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf11 | Mm_Celera | 4:109464847 | CAACTTGGTGGTAAT[C/T]TTCAACTGGAAACTG | 29864 |
| rs28131932 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109464690 | TCCATTAGTCACTTA[C/G]ACTAAGAGTTTGTCC | 29864 |
| rs28131933 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Rnf11 | Mm_Celera | 4:109464611 | AAATGTAGGTAAAAC[A/T]AAGCTCTTTAGAGAA | 29864 |
| rs28131934 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf11 | Mm_Celera | 4:109464362 | GACTATGTCAGACAA[C/T]ATAAAACTCTTAGAA | 29864 |
| rs28131935 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109463871 | CATCTGAGCCTTCTC[C/T]AGGATCACGTGGACA | 29864 |
| rs28131936 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rnf11 | Mm_Celera | 4:109463823 | GTCAAAAGACAGTCC[A/G]TTACGATCTTTGTGT | 29864 |
| rs28131937 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109463742 | ACCTGACTTTATATG[A/T]CTTTGGTATTCAAAG | 29864 |
| rs28131938 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109463144 | GCCACCACTGCCTGG[C/T]CTCAGTTTCACTTTT | 29864 |
| rs28131939 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109462957 | AGCCCAGTCTATATT[C/T]GAACTCACATAAAAC | 29864 |
| rs28131940 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf11 | Mm_Celera | 4:109461421 | TCTTGTGAAATACCC[A/C]CACACAGACATATTT | 29864 |
| rs28131941 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109460497 | GGGAATATGATACAA[C/T]TTCCGAAACTAAAAC | 29864 |
| rs28131942 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109459915 | ACACAATATACAATG[A/G]ACAGAAAACAATATG | 29864 |
| rs28131943 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf11 | Mm_Celera | 4:109459671 | GATTAAAAACTGTCT[C/T]ATCAAACCATCATTT | 29864 |
| rs28131944 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109459301 | AGCCCACTCTATGAT[G/T]ACCTCACTTAAGTCT | 29864 |
| rs28131945 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109458974 | TTCATAGAAGTTCAG[A/C]CCTGGCACTTAAGTA | 29864 |
| rs28131946 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109458869 | CAAAAGCAAACTATA[C/T]TTCTGCTCCTTCAAC | 29864 |
| rs28131947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109458854 | GATTTAACTTGGGTC[C/T]AAAAGCAAACTATAT | 29864 |
| rs28131948 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf11 | Mm_Celera | 4:109458586 | GTACTTTGGTACACT[A/G]GCTGTAACCTTTTCT | 29864 |
| rs28131949 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109458214 | CTACTTTCCTCGGGG[C/T]TTCATTTCAGTTTAT | 29864 |
| rs28131950 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf11 | Mm_Celera | 4:109458050 | TTTCTTTTAAGCCAA[A/G]GGCTCTCTATGCAGA | 29864 |
| rs28131951 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109457660 | GCTCTGACTGCAGAA[A/C]ATCATTTCTTTTTTT | 29864 |
| rs28131952 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109457259 | ACCCTTTAACCACGA[A/T]AACTAATAATGTTGG | 29864 |
| rs28131953 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf11 | Mm_Celera | 4:109457213 | TATGACTATATCGTA[C/T]TGATTTTAGACACTT | 29864 |
| rs28131954 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Rnf11 | Mm_Celera | 4:109457166 | AGGAAAATGAACCCC[C/G]AGATAAGTGAGAGGT | 29864 |
| rs28131955 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109457119 | AAAACTTATTTTCTA[C/T]GGTGTACTAAATTAA | 29864 |
| rs28131956 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109455818 | TGTCTGTTAGCACAA[A/T]GTGAGCAGTGATCTC | 29864 |
| rs28131957 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109455046 | TTCACTTTCAAGTCC[A/G]CTACACTTTTCTACA | 29864 |
| rs28131958 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf11 | Mm_Celera | 4:109454705 | CATACTGTGCCTAAA[A/C]TTGTTACACATTACA | 29864 |
| rs28131959 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf11 | Mm_Celera | 4:109454511 | AGCAAAATATTCATA[C/T]ACCTAAAACTTTTTT | 29864 |
| rs28131960 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf11 | Mm_Celera | 4:109454492 | GTTAATCTAAATACA[C/T]ACAAGCAAAATATTC | 29864 |
| rs28131961 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453849 | CTTGACCCAAATGTC[A/G]GTAACTTTTCAGAAA | 29864 |
| rs28131962 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453592 | CAGTTTGCTTACAAG[C/G]TAGGAGATCACTGTG | 29864 |
| rs28131963 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453231 | CTGTAACTTCAATAA[C/T]CTCAGCACTACAGTA | 29864 |
| rs28131964 | snp | C/G | 0.260355 | 0.249785 | utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109453202 | CTTTTCTAGGAAACA[C/G]ACCAGATGTGTTTCT | 29864 |
| rs28131965 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109452640 | ACAATTTAACAGAAC[C/T]TGATAGTCTAATTTC | 29864 |
| rs31757214 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf11 | Mm_Celera | 4:109462221 | CTCCAGCATGTATTA[A/G]AACTATTTTTTATTT | 29864 |
| rs31834955 | snp | A/T | 0.5 | 0 | intron-variant | Rnf11 | Mm_Celera | 4:109478573 | CAATCAAACAAAAAA[A/T]TTTTTTTTTTGAAAT | 29864 |
| rs31953483 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf11 | Mm_Celera | 4:109471530 | CAACAATGAGAACTT[C/T]TGAAATGTTTAATAT | 29864 |
| rs32460012 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf11 | Mm_Celera | 4:109456270 | CATTACGGGTGGTTG[G/T]GAGCCACCATGTGGT | 29864 |
| rs32467437 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | Rnf11 | Mm_Celera | 4:109478305 | GAGTTCGAGGCCAGT[A/C]TGGTCTGTAATACAA | 29864 |
| rs32695181 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf11 | Mm_Celera | 4:109464619 | GTAAAACAAAGCTCT[C/T]TAGAGAATCTAGCTT | 29864 |
| rs46051278 | snp | C/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109467594 | GCCCACCTTGGGCTA[C/T]AGTGAAACTATATCT | 29864 |
| rs47864106 | snp | C/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109467144 | TTAGTTTGACTCTAC[C/T]GCCCAAATTAAAGGT | 29864 |
| rs49798562 | snp | A/G | | | intron-variant | Rnf11 | Mm_Celera | 4:109478697 | GCTAGGACTAAAGGT[A/G]TGTGCCACCACACCC | 29864 |
| rs50972191 | snp | C/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109470858 | CTCTGATTATCACAT[C/T]TAAGCCATGCACCCA | 29864 |
| rs51944685 | snp | A/G | | | intron-variant | Rnf11 | Mm_Celera | 4:109478659 | GCCTCAAACTCAGAG[A/G]TCTACCTGTCTGTCT | 29864 |
| rs52209862 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rnf11 | Mm_Celera | 4:109478482 | TAGAGCCAAGACAGG[A/T]ACATGTCTAGTTCAA | 29864 |
| rs52490340 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf11 | Mm_Celera | 4:109478465 | CCTGTAATTCAAGCA[C/T]TTAGAGCCAAGACAG | 29864 |
| rs211807286 | in-del | -/GG | | | intron-variant | Rnf11 | Mm_Celera | 4:109461016 | AGAGCACCCCACCTA[-/GG]GGGAGATAGACTGGT | 29864 |
| rs211869067 | in-del | -/AT | | | intron-variant | Rnf11 | Mm_Celera | 4:109463475 | TATACATACATATAC[-/AT]ATATATATATGCAAC | 29864 |
| rs212039981 | in-del | -/C | | | intron-variant | Rnf11 | Mm_Celera | 4:109454892 | TGAGTTTTACTCCAG[-/C]TTGATCTACATAGAG | 29864 |
| rs212059652 | in-del | -/AGGCT | | | intron-variant | Rnf11 | Mm_Celera | 4:109473002 | ACACTCAGGAGGCTG[-/AGGCT]AGGTCAGGAGCTTAA | 29864 |
| rs212081076 | snp | A/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109482013 | TAGGGCCTTATGCAT[A/T]CGGGGCAAGCATTCT | 29864 |
| rs212151412 | snp | C/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109467337 | GTCAACATAAAATGA[C/T]TTAACATTCACTTGA | 29864 |
| rs212173551 | snp | A/G | | | intron-variant | Rnf11 | Mm_Celera | 4:109481014 | ACAGGTTAGCTCTCT[A/G]GATTAGTGGCTATAT | 29864 |
| rs212277707 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Rnf11 | Mm_Celera | 4:109452483 | TAATACTTGATGACA[C/T]ACAAGTGTATAATTA | 29864 |
| rs212278298 | in-del | -/TTTTTA | | | intron-variant | Rnf11 | Mm_Celera | 4:109466055 | GTAGGGCAAGTTTTG[-/TTTTTA]TTTTTGTTTTTTTCA | 29864 |
| rs212461242 | snp | A/G | | | intron-variant | Rnf11 | Mm_Celera | 4:109469332 | TCATTTAATTAAAAG[A/G]TATGTTTGTAAGACT | 29864 |
| rs212581159 | snp | A/G | | | intron-variant | Rnf11 | Mm_Celera | 4:109484601 | AATAAATTCTTATGA[A/G]TGATGTTCATACCAG | 29864 |
| rs212670237 | snp | A/G | | | intron-variant | Rnf11 | Mm_Celera | 4:109471270 | AAGGTGGAAGGGAGA[A/G]GGTAGAGAAGACATC | 29864 |
| rs212728171 | in-del | -/ACCCA | | | intron-variant | Rnf11 | Mm_Celera | 4:109476026 | CGCCACCCCCCCCCC[-/ACCCA]CCCCCGGTCTAGGCC | 29864 |
| rs212855016 | snp | C/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109456529 | TTAAAAGAGGTTTAA[C/T]TCCTATTTATTTACA | 29864 |
| rs212903156 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | Rnf11 | Mm_Celera | 4:109476924 | ACGCTGTCTGCCGGG[-/T]TGATGTCTGTAAGCA | 29864 |
| rs213054201 | snp | C/T | | | upstream-variant-2KB | Rnf11 | Mm_Celera | 4:109485504 | TGCCTGTTTAGTTCT[C/T]TGTGTAGGGTTGAGG | 29864 |
| rs213109252 | snp | A/C | | | intron-variant | Rnf11 | Mm_Celera | 4:109473100 | AAATGAGAATCAATA[A/C]ATTAAGGGCTTCATG | 29864 |
| rs213192283 | snp | A/T | | | intron-variant | Rnf11 | Mm_Celera | 4:109474985 | GTAAGTGTAGAAGGT[A/T]CATGGGGGACGTATC | 29864 |