SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs263550589 | in-del | -/TACCTACCTACCTACCAACCTACCTACCTACA | | | intron-variant | Eed | GRCm38.p3 | 7:89964152 | ACCTACCTACCTACC[lengthTooLong]TACCTACCTATCCAC | 13626 |
rs263622040 | snp | A/T | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982843 | AATAAGATAGAATAA[A/T]AAAAAAAACCCAAAA | 13626 |
rs263625880 | snp | C/T | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982573 | AGTGTCTTAGTCTTT[C/T]AGAGGAAGTTTATGT | 13626 |
rs263765420 | snp | C/T | | | intron-variant | Eed | Mm_Celera | 7:89964985 | GGCTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 13626 |
rs263825910 | snp | A/C | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982855 | taaaaaaaaaaaccc[A/C]aaacacctctcatcg | 13626 |
rs263885020 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89962644 | CATCAGTTTTCCATG[A/C]TAATGCTCTACTGTC | 13626 |
rs263888080 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89970519 | ACCTTCCAAACAACT[A/G]GTAAGAGTTTGGATA | 13626 |
rs263953594 | in-del | -/TC | | | intron-variant | Eed | Mm_Celera | 7:89973406 | TTATCTTGAATTATA[-/TC]TTTATAACCTTGGAC | 13626 |
rs263977249 | in-del | -/G | | | intron-variant | Eed | Mm_Celera | 7:89960894 | TTAATCCCCAGGGTT[-/G]GGGGGGCTTCACTAG | 13626 |
rs264052346 | in-del | -/TTTTTTT | | | intron-variant | Eed | Mm_Celera | 7:89964981 | CTTGGCTTTTCTTTC[-/TTTTTTT]TTTCTTTTTTTTTTT | 13626 |
rs264058086 | in-del | -/A | | | intron-variant | Eed | Mm_Celera | 7:89976573 | TAGGGACCAGTTAAC[-/A]AGATCACACTCAGTT | 13626 |
rs264066149 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89960531 | ATGGTAGTATTAAAT[A/G]ATATCAATGATACAG | 13626 |
rs264243334 | in-del | -/C | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89981839 | GGGCTTCGTTATAGA[-/C]CCTCTTTCCAAAAAT | 13626 |
rs264359418 | snp | A/T | | | intron-variant | Eed | Mm_Celera | 7:89967627 | CAGGCTGCATGAAGC[A/T]GACATGTTTGCCTAC | 13626 |
rs264382156 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89973051 | GAGCTCAGAGGACAT[A/G]GTTATTTCTCTCATC | 13626 |
rs264389535 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89968480 | TAAAGTACATACTTA[A/G]AAGTATAAATATAAG | 13626 |
rs264391329 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89971848 | AATTCTAACTTAAGG[A/G]CATTACAGAAACTAA | 13626 |
rs264489324 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89972600 | TAGCCTTGAGGTTTC[A/C]AAAGCTCACACCAGG | 13626 |
rs264505172 | in-del | -/TTAACAT | | | intron-variant | Eed | GRCm38.p3 | 7:89975849 | AGGCTCTTTCCTCCC[-/TTAACAT]TCACCCATCCCTCGT | 13626 |
rs264560418 | in-del | -/AAG | | | intron-variant | Eed | Mm_Celera | 7:89959629 | GGAGGGAGGGAGGAA[-/AAG]AAGAAGAGAGATATC | 13626 |
rs264568052 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89967033 | GCCAGAGGGAGTATA[A/G]TGAAAACCTTGCTGC | 13626 |
rs264722360 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89975921 | ATGCTGTCAGAGACC[A/G]CACTAGATTCTAGGA | 13626 |
rs264791768 | snp | G/T | | | intron-variant | Eed | Mm_Celera | 7:89974751 | GGAGGGAAAATAGAC[G/T]CCAGAGGTCAGAGGA | 13626 |
rs264806569 | in-del | -/C | | | intron-variant | Eed | GRCm38.p3 | 7:89963061 | ATATATTAAAAAAAA[-/C]AAACAGGTTAAGCTC | 13626 |
rs264813466 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89966577 | CACGACATGGGCGAG[A/C]ACTGTGGCAAGTGCA | 13626 |
rs264881142 | snp | C/T | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982218 | CCAGTCTGTAGCCAG[C/T]CTGTAGCCAGCCTGT | 13626 |
rs265047085 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89978561 | CTAAACTGGCCTCTT[A/G]AATTGAAATCATTTT | 13626 |
rs265090788 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89976733 | ACATTCAAAGTAAAG[A/G]ACAAGGATAAACAAA | 13626 |
rs265127782 | in-del | -/CT | | | intron-variant | Eed | Mm_Celera | 7:89974819 | GTAAATGCACTGTAG[-/CT]CTGTCTTCAGACACT | 13626 |
rs265184173 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89958467 | AGTCTGGGGAGAGGG[A/G]TGGCACTGTAAAGCC | 13626 |
rs265254113 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89957207 | AAACAGTTTAACCAC[A/G]GCGCCACAGAAAGAT | 13626 |
rs265298685 | snp | C/T | | | downstream-variant-500B | Eed | Mm_Celera | 7:89954494 | CTTTGATGCTGCTCT[C/T]TTACAAGAATTGCCT | 13626 |
rs265309658 | snp | C/T | | | intron-variant | Eed | Mm_Celera | 7:89962601 | TTTAGAGCCAATGTA[C/T]CCATTTTTCAGTTGT | 13626 |
rs265355192 | in-del | -/T | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89981901 | TCATAATTCATAGTC[-/T]TAAGTGTTCGTTTTA | 13626 |
rs265361252 | snp | A/G | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982480 | TCATTTGTCATTTGT[A/G]AAATGAAGAGGTAGA | 13626 |
rs265433320 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Eed | Mm_Celera | 7:89981112 | TCGGGAGAACAACTT[C/T]GAGTTAGTGTTTACG | 13626 |
rs265500942 | in-del | -/C | | | intron-variant | Eed | Mm_Celera | 7:89972218 | GCCAACCTGCCCCCA[-/C]CCCGACACTCACTCT | 13626 |
rs265519582 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89967163 | CATCAGAAGACTTCC[A/C]CATGGGCAGTGGTGG | 13626 |
rs265562435 | snp | C/T | | | intron-variant | Eed | Mm_Celera | 7:89959121 | TCTCAAATTAAGTGT[C/T]ACATAGTTTCTGTAC | 13626 |
rs265633654 | snp | C/G | | | intron-variant | Eed | Mm_Celera | 7:89957921 | TAGCTGCCTTACACT[C/G]CTTTCTGCCACGACT | 13626 |
rs265721472 | in-del | -/TG | | | intron-variant | Eed | Mm_Celera | 7:89976232 | CCTCACACAGACATA[-/TG]TGTGCAGGCAAAATA | 13626 |
rs265725351 | in-del | -/CAGCCC | | | intron-variant | Eed | Mm_Celera | 7:89959739 | ACACACACACAGACA[-/CAGCCC]CCCTCCCCCCCTTAT | 13626 |
rs265733552 | snp | C/T | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89983150 | AGTTGATCAGCCCAC[C/T]AGCTCACCTGTGCCC | 13626 |
rs265851572 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89970759 | CACACTTCTTTCTAG[A/G]TGCCTGTGGAAGTAG | 13626 |
rs265861491 | in-del | -/AAACAAACA | | | intron-variant | Eed | Mm_Celera | 7:89979293 | CTCAAACAAACAAAC[-/AAACAAACA]AAAAAATCCCTTTTT | 13626 |
rs265894807 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89963201 | ATGAATGTGCCTGCA[A/G]AGATTAAAGGAGAAC | 13626 |
rs265939397 | snp | A/T | | | intron-variant | Eed | Mm_Celera | 7:89961186 | ACACAGACATCTATG[A/T]GGGCAAAACACTCAT | 13626 |
rs266101579 | snp | C/T | | | intron-variant | Eed | Mm_Celera | 7:89968178 | AGGGGTCTGATTGAG[C/T]AAGAGGACTTGACTT | 13626 |
rs266112498 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89973400 | TTTAAATTATCTTGA[A/G]TTATATCTTTATAAC | 13626 |
rs266175188 | snp | A/G | | | intron-variant | Eed | Mm_Celera | 7:89966420 | GCTGACAGGTTCCTG[A/G]TTACAATGTATCAGC | 13626 |
rs386860593 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89961155 | CCTCTGAGGGCACCA[A/G]AGACACATAAATGGT | 13626 |
rs386934151 | in-del | -/ACACACACACACACACAC | | | intron-variant | Eed | Mm_Celera | 7:89962192 | CACACACACACACAC[-/ACACACACACACACACAC]GCAGGCACGCACAAT | 13626 |
rs386977762 | in-del | -/GGCTACACAG | | | intron-variant | Eed | Mm_Celera | 7:89971784 | TTCCAGGATAGCCAG[-/GGCTACACAG]AGAAACCCTGTCTTG | 13626 |
rs387009670 | in-del | -/A | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982858 | AAAAAAAAACCCAAA[-/A]CACCTCTCATCGTGG | 13626 |
rs387115557 | in-del | -/ACACACACACACAC | | | intron-variant | Eed | Mm_Celera | 7:89962160 | TTTCCTGAACAGTGT[-/ACACACACACACAC]ACACACACACACACA | 13626 |
rs387165579 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89958952 | AAGCCTTGCAAGCTG[A/G]GTGCAATGCCCAGAT | 13626 |
rs387299496 | in-del | -/GTAGCCAGCCT | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982232 | GCCTGTAGCCAGCCT[-/GTAGCCAGCCT]TAACCACTGAGCCAG | 13626 |
rs387323827 | in-del | -/AAATAAATAAAT | | | intron-variant | Eed | Mm_Celera | 7:89965689 | AATAAATAAATAAAT[-/AAATAAATAAAT]CTTTTTAAAAAATTT | 13626 |
rs387460447 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Eed | GRCm38.p3 | 7:89981119 | AACAACTTCGAGTTA[A/G]TGTTTACGGAACTTC | 13626 |
rs387495942 | in-del | -/TCTTAGACTGCCCAGCTAGCAAGCTCTATTGCCCAACCCTGGGTTTA | | | intron-variant | Eed | Mm_Celera | 7:89963296 | CTAAAGCCAGTGGGT[lengthTooLong]TCTTAGACTGCCCAG | 13626 |
rs387533435 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89955219 | AATCCCAGTGCTTGG[A/G]AGGCAGAGGCAGAGG | 13626 |
rs387538174 | in-del | -/AA | | | intron-variant | Eed | Mm_Celera | 7:89968457 | CTACCCATAAAAAAA[-/AA]GATTTTTAAAGTACA | 13626 |
rs387637432 | in-del | -/T | | | intron-variant | Eed | Mm_Celera | 7:89967065 | AAAGCACAAACTACA[-/T]TTTTTTTTTTTATAA | 13626 |
rs387700330 | in-del | -/AA | | | intron-variant | Eed | Mm_Celera | 7:89957268 | CTCTTCAGATTTAAA[-/AA]GTCTTAATGCTAAGA | 13626 |
rs387778924 | in-del | -/A | | | upstream-variant-2KB | Eed | Mm_Celera | 7:89982851 | AGAATAAAAAAAAAA[-/A]CCCAAAACACCTCTC | 13626 |
rs387889394 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89960040 | CTAAATCCCAAATGG[C/T]TGGGCACACCTGTGA | 13626 |
rs578304610 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974607 | AGGGGAGAGGCAGAA[C/T]CTGTATTATTTTGAT | 13626 |
rs578317591 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89966582 | CATGGGCGAGCACTG[C/T]GGCAAGTGCACATCC | 13626 |
rs578401238 | snp | G/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971757 | TCCAGGACAGCCTGG[G/T]CTACAAAGTGAGTTC | 13626 |
rs578689940 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89965930 | CACATTACAAACATT[A/T]AAAAATATCAAAAAA | 13626 |
rs578862273 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971341 | ATCTTACCCTACCCA[C/T]TTCATCACACATCTT | 13626 |
rs578870939 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89962160 | TTTCCTGAACAGTGT[A/T]CACACACACACACAC | 13626 |
rs579291985 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89978281 | AAGTTACTGCTCCCT[A/C]AAGTTGGTTTTGTAT | 13626 |
rs579378035 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89965351 | CATCGCCTCAGCTTG[C/T]CAGAAGTCACAGACT | 13626 |
rs579397408 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89974803 | TTATTTATTTATTAC[A/G]TGTAAATGCACTGTA | 13626 |
rs579489155 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89955259 | TTCTGAGTTCCAGGA[C/T]AGCCAGGGCTACACA | 13626 |
rs579520157 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89975545 | GCTACACAGAAAAAC[C/T]CTGTCTCAAAAAAAC | 13626 |
rs579668416 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89963386 | TTGCCCAACCCTGGG[C/T]TTATCAGCAAGTCAA | 13626 |
rs579963565 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89972676 | CTCTCAGCCACCTCT[C/T]CAGCATCAAGTCTGC | 13626 |
rs580013065 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89964168 | ACCTACCTACCTACC[A/T]ACCTACCTACCTACA | 13626 |
rs580046220 | snp | A/G | | | upstream-variant-2KB | Eed | GRCm38.p3 | 7:89983234 | GCAGTAAGAAAAAAA[A/G]AAGAAGAAGAAGAAG | 13626 |
rs580092530 | snp | C/G | | | intron-variant | Eed | GRCm38.p3 | 7:89972124 | AGTTTCTTACACAAA[C/G]AGTCATACTGTTAAC | 13626 |
rs580106917 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89974893 | CCATGTAGTTGCTGG[A/G]ATTTGAACTCAGGAC | 13626 |
rs580200692 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89968445 | AACCATATACATCTA[C/T]CCATAAAAAAAAAGA | 13626 |
rs580591453 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89970089 | TTCCAGGACAGCCAG[A/G]GCTATACAGAGAAAC | 13626 |
rs580644984 | snp | C/G | | | intron-variant | Eed | GRCm38.p3 | 7:89958890 | ACAAAGAAATATGCT[C/G]CACACGGGCCAGCAA | 13626 |
rs580654865 | snp | G/T | | | intron-variant | Eed | GRCm38.p3 | 7:89976133 | TTCCCCGATCCAAGA[G/T]AACCAAGTCAGTTTG | 13626 |
rs580684751 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89973521 | CACGGGGAGAACAAC[A/C]TGTGAGATTTCTGTC | 13626 |
rs580717188 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89960727 | TATATACATATACAT[A/G]TATGTGTATGTGTAT | 13626 |
rs580718887 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89978233 | GAGTGTATCCAACAG[C/T]CGTTAGAGTGAAGCC | 13626 |
rs580761856 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89965229 | CCAGGCTGGCCTTGA[A/C]CTCAGAAATCCGCCT | 13626 |
rs580869415 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974217 | TTATGACTTTTTTTT[C/T]CTGTATATCATGAAC | 13626 |
rs581187883 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89965536 | TAAGAACACCCGACT[A/G]CTCTTTCGAAGGTCC | 13626 |
rs581263644 | snp | C/G | | | intron-variant | Eed | GRCm38.p3 | 7:89976783 | TGACAGATTAGAATA[C/G]TCAACTTAAACAAAC | 13626 |
rs581339410 | snp | C/G | | | intron-variant | Eed | GRCm38.p3 | 7:89959730 | AACAACAACAACACA[C/G]ACACAGACACCCTCC | 13626 |
rs581352812 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974214 | GCTTTATGACTTTTT[C/T]TTTCTGTATATCATG | 13626 |
rs581471624 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971397 | CACCTCCTAACAAGT[C/T]CAACATCAGGTAGAT | 13626 |
rs581741844 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89971326 | GCTCCTTCTTCCGTC[A/G]TCTTACCCTACCCAT | 13626 |
rs581744659 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971729 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCC | 13626 |
rs582021176 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974779 | GGATAACATAAAGTT[A/T]TTTAAGATTTATTTA | 13626 |
rs582071414 | snp | G/T | | | intron-variant | Eed | GRCm38.p3 | 7:89975405 | AACAAAACAAAACCA[G/T]CCCACCCCCATCTTA | 13626 |
rs582145812 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89965990 | GGAAGGTGGCACACA[C/T]GAGCCATGGCACATG | 13626 |
rs582522574 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89955212 | CACCTTTAATCCCAG[C/T]GCTTGGGAGGCAGAG | 13626 |
rs582525083 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89974805 | ATTTATTTATTACGT[A/G]TAAATGCACTGTAGC | 13626 |
rs582553079 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89962670 | CTGTCCTTTTTAAAC[C/T]CAGGATTTCAAGTTT | 13626 |
rs582658785 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971761 | GGACAGCCTGGTCTA[C/T]AAAGTGAGTTCCAGG | 13626 |
rs582707508 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89961873 | AAGGTAGAGCAAACT[A/G]CAGCCTGTAAGCCAA | 13626 |
rs582910349 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89972717 | CTTTGCTTCCAGCCA[A/T]GATATAATAACTAAA | 13626 |
rs583179647 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89970137 | AAATAAACAAACCAA[C/T]AAACAAATAATAAAT | 13626 |
rs583238578 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89975959 | CTGTAGAACCCACCC[A/C]CAAGGTCACATATAC | 13626 |
rs583655767 | snp | C/G | | | intron-variant | Eed | GRCm38.p3 | 7:89964147 | TACCTACCTACCTAC[C/G]TACCTACCTACCTAC | 13626 |
rs583659654 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89958895 | GAAATATGCTCCACA[C/T]GGGCCAGCAAGATGG | 13626 |
rs583752677 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89964196 | ACATACCTACCTATC[C/T]ACGTATCTAGGGGGT | 13626 |
rs583846271 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89972404 | TAACTCTTACCCTTC[C/T]TTCTCTCCCCCAAAT | 13626 |
rs584036351 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89976245 | TATGTGTGCAGGCAA[A/G]ATAGCAATGTCCATA | 13626 |
rs584342479 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89974600 | CTCTGACAGGGGAGA[A/G]GCAGAATCTGTATTA | 13626 |
rs584461733 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89960780 | ACACACAAACGGTTT[A/C]TCTGAGAGTGTGCTG | 13626 |
rs584465476 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89978234 | AGTGTATCCAACAGT[C/T]GTTAGAGTGAAGCCC | 13626 |
rs584558725 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89971400 | CTCCTAACAAGTCCA[A/G]CATCAGGTAGATGCC | 13626 |
rs584648936 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89965081 | CCAGGCTGGCCTCGA[A/C]CTCAGAAATCCGCCT | 13626 |
rs584794923 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89965340 | CACATTCCAGGCATC[A/G]CCTCAGCTTGCCAGA | 13626 |
rs584964731 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89965642 | TGAAGACAGCTACAG[C/T]GTACTTACATTAAAT | 13626 |
rs585026718 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974215 | CTTTATGACTTTTTT[C/T]TTCTGTATATCATGA | 13626 |
rs585168049 | snp | A/C | | | intron-variant | Eed | GRCm38.p3 | 7:89962152 | AGTAACTGTTTCCTG[A/C]ACAGTGTACACACAC | 13626 |
rs585187494 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974782 | TAACATAAAGTTATT[A/T]AAGATTTATTTATTT | 13626 |
rs585219678 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971338 | GTCATCTTACCCTAC[C/T]CATTTCATCACACAT | 13626 |
rs585361163 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89962684 | CTCAGGATTTCAAGT[C/T]TGGGGTAGGTGAGAC | 13626 |
rs585463288 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89975449 | CAAAAACCAAAACCA[A/T]CCCCTGCCTTTTAAT | 13626 |
rs585572611 | snp | A/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971754 | AGTTCCAGGACAGCC[A/T]GGTCTACAAAGTGAG | 13626 |
rs585634246 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89963339 | TTGCCCAACCCTGGG[C/T]TTATCTTAGACTGCC | 13626 |
rs585682478 | snp | C/T | | | upstream-variant-2KB | Eed | GRCm38.p3 | 7:89982207 | CCAGCCTGTAGCCAG[C/T]CTGTAGCCAGCCTGT | 13626 |
rs585813429 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89972468 | TTTGGCTAAGAATGG[C/T]CCACATAGGCTCATA | 13626 |
rs585820316 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89955213 | ACCTTTAATCCCAGT[A/G]CTTGGGAGGCAGAGG | 13626 |
rs585923578 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89967180 | ATGGGCAGTGGTGGC[A/G]CACAGACTTCCCCAA | 13626 |
rs586011632 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89968437 | CCACATATAACCATA[C/T]ACATCTACCCATAAA | 13626 |
rs586286793 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89955214 | CCTTTAATCCCAGTG[C/T]TTGGGAGGCAGAGGC | 13626 |
rs586299100 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89974809 | ATTTATTACGTGTAA[A/G]TGCACTGTAGCTGTC | 13626 |
rs586498861 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89971798 | AGAGAAACCCTGTCT[C/T]GAAAAACCAAAAGAA | 13626 |
rs586536801 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974216 | TTTATGACTTTTTTT[C/T]TCTGTATATCATGAA | 13626 |
rs586626873 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89978225 | TTTTGTCTGAGTGTA[C/T]CCAACAGTCGTTAGA | 13626 |
rs586632990 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89965208 | TCCTGGAACTCACTC[C/T]GTAGACCAGGCTGGC | 13626 |
rs587009285 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89960500 | CACTACACATCTATT[A/G]GAACAACTAAAAATA | 13626 |
rs587027628 | snp | G/T | | | intron-variant | Eed | GRCm38.p3 | 7:89965014 | TTTTTTTGCTTTTTC[G/T]AGACAGGGTTTGTCT | 13626 |
rs587109880 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89976481 | TTAAAAAATGTCACA[C/T]TGTTTTGTTAAAAGG | 13626 |
rs587482351 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89974213 | AGCTTTATGACTTTT[C/T]TTTTCTGTATATCAT | 13626 |
rs587506298 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89964150 | CTACCTACCTACCTA[C/T]CTACCTACCTACCTA | 13626 |
rs864308393 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Eed | GRCm38.p3 | 7:89954775 | GTAAAGTCCGAGCAG[A/G]AAGACAGTACAAAGA | 13626 |
rs864309008 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89962499 | CAAACCAGGCAAGCA[C/T]TCTGCCTGCTGAGCT | 13626 |