| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3696331 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rnf220 | Mm_Celera | 4:117410810 | ATGAAGGACATGCCC[A/G]GGCGTGATGAATCCC | 66743 |
| rs3705529 | snp | A/G | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117309668 | TGGGGCTGGAATTAC[A/G]TAGATGGATGTGTTT | 66743 |
| rs3705654 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rnf220 | Mm_Celera | 4:117309749 | CTAGTAGGTCTCACT[A/G]CTTCTCCTTGGTAAC | 66743 |
| rs3707238 | snp | C/T | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117309979 | AACCAACCAACATTT[C/T]TCCAATACATATGAT | 66743 |
| rs3724818 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Rnf220, LOC102637578 | Mm_Celera | 4:117497242 | TCTCCTCCTTTCCCT[C/T]CGGAGAAATCTGACT | 66743 |
| rs4224732 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf220 | GRCm38.p3 | 4:117285336 | TGGCACTCTGGTGAC[C/T]AGGTCACTTCTGGTA | 66743 |
| rs6152515 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337800 | TCCTCAAAGGCTTCA[A/G]AGCTCTTCTGTAACA | 66743 |
| rs6153109 | snp | A/T | 0.5 | 0 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337933 | ttcctctcagttagt[A/T]tgaggatttnatgac | 66743 |
| rs6153125 | snp | C/T | 0.5 | 0 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337943 | ttagtntgaggattt[C/T]atgactttgcanatg | 66743 |
| rs6153540 | snp | C/T | 0.5 | 0 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337955 | tttnatgactttgca[C/T]atgcgaaatgcttag | 66743 |
| rs6183342 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rnf220 | Mm_Celera | 4:117383831 | GTGGACAACAAGAAG[A/G]CCACCAATGGCCACC | 66743 |
| rs6183477 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Rnf220 | Mm_Celera | 4:117383902 | AGGAATGCAGCTCCT[G/T]AGCTCCTTGCACAAC | 66743 |
| rs6183920 | snp | C/T | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117383927 | CACAACCTCCTGGTG[C/T]AGCAAGNGCCTAAGT | 66743 |
| rs6183926 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rnf220 | Mm_Celera | 4:117383934 | TCCTGGTGNAGCAAG[C/G]GCCTAAGTCAGACGG | 66743 |
| rs6185101 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Rnf220 | Mm_Celera | 4:117384166 | AATGGCCTGTATATG[A/T]ATCTGATGTTCATCT | 66743 |
| rs6185724 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rnf220 | Mm_Celera | 4:117384297 | CAGCATAAGAACCAG[A/G]TAGGAGAGACACGGC | 66743 |
| rs6231278 | snp | G/T | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117471124 | GTTGCTGTGCTAAAT[G/T]TTGGGGGACAGCANC | 66743 |
| rs6231306 | snp | C/T | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117471138 | TNTTGGGGGACAGCA[C/T]CAGAAATGGTGGCCA | 66743 |
| rs6252193 | snp | A/G | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117328709 | AGCTGGGGAAATGTC[A/G]ACAGANAGAAGCTCC | 66743 |
| rs6252203 | snp | G/T | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117328715 | GGAAATGTCNACAGA[G/T]AGAAGCTCCTGGAAG | 66743 |
| rs6252628 | snp | A/T | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117328773 | AGACGGCTATAAGCT[A/T]NGGAAAAGGAGTGGC | 66743 |
| rs6252630 | snp | A/G | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117328774 | GACGGCTATAAGCTN[A/G]GGAAAAGGAGTGGCA | 66743 |
| rs6253179 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf220 | Mm_Celera | 4:117328896 | GCTTTGCATCCGATC[A/G]CAGGCTTCCTGCGGG | 66743 |
| rs6379152 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Rnf220, LOC102637763 | Mm_Celera | 4:117302673 | GAGGCTGTTTCCCGG[C/T]CCAGGGGCCAGCTTT | 66743 |
| rs6379244 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Rnf220, LOC102637763 | Mm_Celera | 4:117302719 | TGAGCTCAGGTCCTA[C/T]CAGCTAAGCCTGTGA | 66743 |
| rs6412212 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337505 | ATGGAGAGGGGCAGA[G/T]TATTAAACAATACCC | 66743 |
| rs6412244 | snp | A/G | 0.5 | 0 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337523 | TTAAACAATACCCAC[A/G]AGCAGCTGACTGTCC | 66743 |
| rs6412284 | snp | A/G | 0.5 | 0 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337543 | GCTGACTGTCCCATA[A/G]GACTGTTCAGCACCA | 66743 |
| rs6412781 | snp | C/T | 0.5 | 0 | intron-variant | Rnf220 | GRCm38.p3 | 4:117337585 | GCCCTAGGGGATGGG[C/T]GCAAGAGTGTATATG | 66743 |
| rs13469324 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf220 | Mm_Celera | 4:117271844 | AGCTGGCTGGGAGCT[C/T]GGCTCAGCCACCTCT | 66743 |
| rs13469325 | snp | C/G | | | utr-variant-3-prime | Rnf220 | Mm_Celera | 4:117271608 | GACTGAGGGTGCCTG[C/G]CTGCCCAGCCTGCGG | 66743 |
| rs13477934 | snp | C/T | 0.440918 | 0.161401 | intron-variant | Rnf220 | Mm_Celera | 4:117358165 | ACTTTCAGCACTGCC[C/T]GAGCTTCCTTCAGGA | 66743 |
| rs27481968 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf220 | Mm_Celera | 4:117420012 | AGTAGGGAGTTTAGA[A/G]AAGGACCACAAGAAA | 66743 |
| rs27481969 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Rnf220 | Mm_Celera | 4:117420005 | AGCAGGAAGTAGGGA[A/G]TTTAGAGAAGGACCA | 66743 |
| rs27481970 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf220 | Mm_Celera | 4:117419542 | GACCCCTCAGAGAGG[A/G]CCTAGGAGCTGGGGC | 66743 |
| rs27481971 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf220 | Mm_Celera | 4:117419415 | GGCAGAGGGGCAGGC[A/G]ACTTCACATAGGAAG | 66743 |
| rs27481972 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117419110 | CCCATGTGGTAGAAC[A/G]GAGTGCAGTCTAACG | 66743 |
| rs27481973 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117419090 | CAGGTATATGGGAGC[A/G]ATGGCCCATGTGGTA | 66743 |
| rs27481974 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf220 | Mm_Celera | 4:117419053 | TATCACTCTGGAAAC[A/G]GGATAATAGAGGACT | 66743 |
| rs27481975 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117419052 | TTATCACTCTGGAAA[C/T]GGGATAATAGAGGAC | 66743 |
| rs27481976 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf220 | Mm_Celera | 4:117418886 | TGATGATAAAGTCTT[C/T]GAGTCCCTGGGAGGA | 66743 |
| rs27481977 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117417849 | TTGATTATTTGGGCT[A/T]CTAAGCTTTAGAAGA | 66743 |
| rs27481978 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf220 | Mm_Celera | 4:117417161 | CAGACTCTGACTTAC[A/T]TATTGAAAGGTCCCA | 66743 |
| rs27481979 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Rnf220 | Mm_Celera | 4:117417108 | ATGAAAGGGGAAGCA[C/T]GAGAAACCGGAGAAT | 66743 |
| rs27481980 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf220 | Mm_Celera | 4:117416311 | CCGTGGATAAAGGTG[A/C]TTGCTGACTAGCCGG | 66743 |
| rs27481981 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf220 | Mm_Celera | 4:117416282 | TGTAGGGAAAGACAG[A/G]GTGCAAGATGGTTCC | 66743 |
| rs27481982 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117416068 | ACAGGCTGCAGCCAC[A/G]GCAGCCACTGCAGCC | 66743 |
| rs27481983 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117415757 | CTGCCTGGCCCACTC[C/T]ATGGTGGCAGAGAAG | 66743 |
| rs27481984 | snp | A/G | 0.5 | 0 | intron-variant | Rnf220 | Mm_Celera | 4:117415730 | CTCCTTGGCCAAACC[A/G]AGAAGTTGGGGCTGC | 66743 |
| rs27481985 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117414847 | GAATACTCATCTCTA[A/G]CCTGTAGCACAGTCA | 66743 |
| rs27481986 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117414459 | ACAAAGCAAACAGCA[C/T]ATAGAGAACTGAGAC | 66743 |
| rs27481987 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117412896 | TCCACCATTTGTAGC[A/G]TCGCCCCAGCGCTAG | 66743 |
| rs27481988 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117411939 | GCGAGCAGTCTGTGC[A/G]GAGGCAGGCGAGAAG | 66743 |
| rs27481989 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117411328 | CTGGGTCCTAGCACA[C/T]AGCTGCCTTGTAAGA | 66743 |
| rs27481990 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117411087 | CCCATGGCTTATACA[A/C]TATCCTTCTTCCACA | 66743 |
| rs27481991 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117411043 | CAGACTGACCCACAC[C/T]TAGGGTCACACCCTA | 66743 |
| rs27481992 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117410870 | AGGTCAACAAAGTCC[C/T]GCTGAGTCCTTGTAG | 66743 |
| rs27481993 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117410701 | CCATAGGGCAGGTAC[A/C]TTATGCTCGATTTTT | 66743 |
| rs27481994 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117410632 | TAGATAGGATGTCCG[A/T]CTCAACCATGCATGG | 66743 |
| rs27481995 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117410606 | CACTTGCATTTGGCT[A/G]GAGAGTGTGGTAGAT | 66743 |
| rs27481996 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117410474 | ATGACTCTCTTCCCA[A/G]GACGGCTATGGTGGC | 66743 |
| rs27481997 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117410394 | AGATGGATGAGTGGT[A/G]TCTCTTTAAGTCAGG | 66743 |
| rs27481998 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf220 | Mm_Celera | 4:117410356 | AAGGAAGAGGATGTG[A/G]CTGGAGGTCAGAGGA | 66743 |
| rs27481999 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117410325 | GAAACGTAGAGGGAG[A/G]CATGAAGTAAGCAGG | 66743 |
| rs27482000 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf220 | Mm_Celera | 4:117409019 | AGTGGAACTTACGAC[A/G]AAGGTCTTGAGGGCC | 66743 |
| rs27482001 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117408994 | GATTGCCATTTTACT[C/T]CATGTTTCGAGTGGA | 66743 |
| rs27482002 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117408940 | TGTGGCTTAGGAACA[A/G]CAAAGAGACCAACTT | 66743 |
| rs27482003 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117408819 | TCAGACCTTTCTACC[A/G]CTGGGGCCCCAGGAA | 66743 |
| rs27482004 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117408732 | GAGTCTTGTTCCCTC[C/T]ACCATAAGGGAGAGT | 66743 |
| rs27482005 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117408665 | GGACACTTTGGGAAA[A/G]GCCCTTAGGTCATCT | 66743 |
| rs27482006 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117408521 | ATCCTGAGTGACCTT[C/T]TGATTTTCTTATCCA | 66743 |
| rs27482007 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117408232 | GAGTGTTCAAGCCTA[G/T]TGGAAAAGAGGCCTT | 66743 |
| rs27482008 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf220 | Mm_Celera | 4:117408179 | GCCCCACGTGGTACT[C/T]ATAGCACAGAGGACC | 66743 |
| rs27482009 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117408104 | TTGGTTTTCATTTTC[C/T]TCACTTCCTCTGAGT | 66743 |
| rs27482010 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117407972 | GCCATCACATTGTCT[A/G]GATCCCTGGCCCCAA | 66743 |
| rs27482011 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf220 | Mm_Celera | 4:117407390 | CACCAGCCTTAATAC[C/T]TCATGATGGATATCA | 66743 |
| rs27482012 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rnf220 | Mm_Celera | 4:117407296 | GCCAGCTTCCTCATG[G/T]TCCCCTTTACTTCCC | 66743 |
| rs27482013 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf220 | Mm_Celera | 4:117407198 | TCTCCAGCCCTTGTG[C/T]ATACTTTCTAACTTG | 66743 |
| rs27482014 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117406588 | CCATAATTAGATGCT[C/T]CAGCCCGGGACTTCC | 66743 |
| rs27482015 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf220 | Mm_Celera | 4:117406514 | AATAGTTCTCTTCAA[C/T]GAACAGAGGGACCTT | 66743 |
| rs27482016 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117406489 | CAGCAAGGCAGCTTC[C/T]AAGACCCTGAATAGT | 66743 |
| rs27482017 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117406447 | TCCCAAGAGTTCTAC[A/G]CCCAAATTTTCTGTG | 66743 |
| rs27482018 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117406089 | CTCCCTGGGCCAGGC[C/T]GCTGTCACACCTTCC | 66743 |
| rs27482019 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117406046 | GTGCTGAAAGCTAAG[A/G]TTCCTTGCACCAGCT | 66743 |
| rs27482020 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117405958 | AAAGCTGGCCTTCTG[C/T]CTCTTCGGGTCACCT | 66743 |
| rs27482021 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf220 | Mm_Celera | 4:117405480 | CCATCACTCTCAGAA[A/G]GAACAAAATTGTTTT | 66743 |
| rs27482022 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117405126 | TGTCTGCATCTATAC[A/T]TCTGTACATCCGTAT | 66743 |
| rs27482023 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117404606 | AAACACTGATCCTCA[C/T]ATTGGCATGCCAAGC | 66743 |
| rs27482024 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117403604 | GAGCATGAGCAGTTT[A/G]TGCCAACACTGTGCT | 66743 |
| rs27482025 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf220 | Mm_Celera | 4:117403587 | GCCAATCTTTACAAC[C/T]GGAGCATGAGCAGTT | 66743 |
| rs27482026 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf220 | Mm_Celera | 4:117403573 | TCCTTGCTGAACGTG[A/C]CAATCTTTACAACCG | 66743 |
| rs27482027 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117403570 | CCCTCCTTGCTGAAC[A/G]TGCCAATCTTTACAA | 66743 |
| rs27482028 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117403555 | TGACTTTAAGCTCCA[C/T]CCTCCTTGCTGAACG | 66743 |
| rs27482029 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117403336 | CTTCAAACACTGAGG[A/C/T]GAAATGTGAAGGGCT | 66743 |
| rs27482030 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf220 | Mm_Celera | 4:117403205 | AGTGCCATGGCTCCA[A/C]CGGTATCATTTCTCT | 66743 |
| rs27482031 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117401582 | AAAGTCAGAGGTTGA[C/T]ATTGAGCATTCTTCT | 66743 |
| rs27482032 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117401557 | TGTGTGTGCACCGTG[A/C]GAGCTTGTGAAAGTC | 66743 |
| rs27482033 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117401256 | AGGAAAATTCCAAGG[C/T]AGCAGCTGTTTCCCT | 66743 |
| rs27482034 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf220 | Mm_Celera | 4:117401244 | AAATCCCAATGGAGG[A/C]AAATTCCAAGGCAGC | 66743 |
| rs27482035 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf220 | Mm_Celera | 4:117401147 | ATTTTAGATTCCAGT[G/T]CAAGGAAACTGTCCT | 66743 |