| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs3657238 | snp | C/T | 0.498866 | 0.0237825 | intron-variant | Lnx1 | GRCm38.p3 | 5:74605619 | TGAAGCCATGATGTT[C/T]TGCTGCGCTGCTGTG | 16924 |
| rs3659100 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Lnx1 | GRCm38.p3 | 5:74605910 | TTTGCCAACAGAAGA[C/G]AGTTATTCCCAACAG | 16924 |
| rs6299799 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652373 | AGGAGAGAGAGAAAA[C/T]CATGAATGAAATTGA | 16924 |
| rs6313089 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652505 | AGGACATCCTTCCAT[A/G]TATGAAGTCAGCAAT | 16924 |
| rs6313107 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652522 | ATGAAGTCAGCAATG[A/G]TCATATCCATGAATG | 16924 |
| rs6330646 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653487 | taatcctagctcttg[A/G]cagaaagcattacaa | 16924 |
| rs6331099 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653533 | ggtcaccctcagcca[C/T]acagcaagttcaagt | 16924 |
| rs13473461 | snp | C/T | | | missense, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74597929 | TCTATTTCAGGTACT[C/T]ATGTAACTGTAAAGA | 16924 |
| rs13473462 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74595128 | AGGCTATGAGCGCCA[C/T]AGAGCTAGTCGGGAG | 16924 |
| rs13473463 | snp | A/G | | | utr-variant-3-prime, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74596065 | TAATGTTTAAGAAAT[A/G]TACCTTTAATCTTGT | 16924 |
| rs13478327 | snp | C/T | 0.498998 | 0.0223656 | synonymous-codon | Lnx1 | GRCm38.p3 | 5:74607852 | GGTCATGCCGAGAGA[C/T]TCGCTGGGGTCTTTC | 16924 |
| rs29502174 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74609507 | GTGCATGGATATTTT[A/G]CCTACTACAGGTATA | 16924 |
| rs29503228 | snp | C/T | 0.375 | 0.216506 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648806 | TTAAGAAAGAAACAA[C/T]TTTCTGAGTAACGCC | 16924 |
| rs29506577 | snp | G/T | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74659903 | GGCTAAATACTAATG[G/T]CTTATTTCAAAAAGA | 16924 |
| rs29506611 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Lnx1 | GRCm38.p3 | 5:74689345 | TCTTGCTTTTAGACA[A/T]ACATGAGCCTAGCTA | 16924 |
| rs29508193 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697376 | TGAACCCTACAGAGA[C/T]GAGGTAAATCTGCCC | 16924 |
| rs29508656 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638648 | GAGGCATAGCAGCTG[C/T]AGCCAAGGTGTAGAC | 16924 |
| rs29509012 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74644857 | GACCCAGGAGGAAAC[A/G]GAGTCCCTAGATTTG | 16924 |
| rs29511368 | snp | G/T | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74621203 | TTCCATGTGTGTGTG[G/T]GGGGGGAGAGAGAGA | 16924 |
| rs29526454 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74639432 | AAACAGCTCCGGGGG[A/G]TGGGGTGGGGGGGCT | 16924 |
| rs29527436 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682116 | GGTAGCCCATATCTG[C/T]GTTGAACTCCCTATA | 16924 |
| rs29527439 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74642560 | TTTTCTGTAAACTGT[C/T]TAGGGATTGGGAATA | 16924 |
| rs29527869 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74647883 | AGGTTTGTCTTGGAC[A/G]GAATCATGGCAGGCC | 16924 |
| rs29532337 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74643075 | ATGTTTTTTACTTCA[A/G]GGTTGATGGGAAACG | 16924 |
| rs29542881 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Lnx1 | Mm_Celera | 5:74696895 | TGTGTATGTGGACAT[C/T]GGCTACAGAATGAGT | 16924 |
| rs29544225 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | GRCm38.p3 | 5:74677326 | CACAAAGCACTAAGC[A/G]TGCTGCTTCAACTGC | 16924 |
| rs29545653 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74667111 | TGAGTGCAGCATGTC[C/T]TCCCTTCTGAGCAGG | 16924 |
| rs29546535 | snp | A/G | 0.188366 | 0.242283 | intron-variant, utr-variant-3-prime | Fip1l1, Lnx1 | Mm_Celera | 5:74592729 | ATGACAGTATGGCAT[A/G]TACATGTAAGTGGGA | 16924 |
| rs29548239 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Lnx1 | Mm_Celera | 5:74611673 | GCCATGGATCGATTT[C/T]CTGTATCTCTGATTG | 16924 |
| rs29549902 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Lnx1 | Mm_Celera | 5:74696883 | GACAGGGATGGCTGT[G/T]TATGTGGACATCGGC | 16924 |
| rs29560463 | snp | A/C | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74655088 | CAGAGGGCCTGGGCT[A/C]TGGAAGGAAGAACTG | 16924 |
| rs29563201 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648328 | CAGACGCTCAGTGTG[C/G]TGTTATCCTGTTTCC | 16924 |
| rs29564836 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Lnx1 | Mm_Celera | 5:74667636 | TAAAGTTAAGGATCT[A/G]CCTTGATATTTTTCC | 16924 |
| rs29565269 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Lnx1 | GRCm38.p3 | 5:74677132 | GTCTGCTTGCAAGCT[A/C]TGGTCTTAATTGCTC | 16924 |
| rs29566096 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Lnx1 | Mm_Celera | 5:74642066 | AGCTAGGGATGTGGT[A/G]GAGGAGTTCCTGGTT | 16924 |
| rs29568252 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Lnx1 | Mm_Celera | 5:74633788 | AACTTTGGATACGCT[A/G]TCTGCTGAAACAAGT | 16924 |
| rs29568542 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Lnx1 | GRCm38.p3 | 5:74609711 | GTTTTTAGTAACAAG[C/T]GCCACAATGGCCTGT | 16924 |
| rs29568613 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74661576 | AGTTACCCTGGCCTC[A/G]TAGTTAGAAGCAGAC | 16924 |
| rs29579422 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682477 | TACAGTATAGAAGTC[A/G]AGGTCAATTTCCTCT | 16924 |
| rs29580542 | snp | A/C | 0.456747 | 0.140554 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74655500 | GATATCGTCTGCAAT[A/C]TGTGGGCTTCTGTTT | 16924 |
| rs29581122 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | GRCm38.p3 | 5:74598555 | CAACTAGGAGAGTCG[C/T]GGCTGTCAGACCTAA | 16924 |
| rs29581360 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74642565 | TGTAAACTGTTTAGG[A/G]ATTGGGAATATGTAC | 16924 |
| rs29582494 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74704394 | AAAAGCAAAAGGTTC[C/G]AAAAGGAGGGAGGGG | 16924 |
| rs29586174 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Lnx1 | Mm_Celera | 5:74660063 | TTGGCAAGTCTGAGG[A/G]CCAGGTTTGCACAAA | 16924 |
| rs29626910 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Lnx1 | GRCm38.p3 | 5:74632609 | ATGCTTCTAACAGTC[C/T]GTAGCATCCTCAATG | 16924 |
| rs29626964 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Lnx1 | Mm_Celera | 5:74660664 | AGCCAAACAGCTGAT[A/G]AACATTCAAGTCCAG | 16924 |
| rs29628632 | snp | A/G | 0.387812 | 0.208586 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74657499 | AGCTCACTCCCATAG[A/G]GCTGGAACTGCCTGT | 16924 |
| rs29629187 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74644474 | AGCCTGCACAGGTTC[C/T]AAGCACTCTATCTCA | 16924 |
| rs29629762 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Lnx1 | GRCm38.p3 | 5:74667922 | GGAGTAACTTGAAGA[C/T]GTGCTAGTAATCCTA | 16924 |
| rs29629859 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74642518 | GGGGAGGGGAGCTGG[A/C]GAGTCCCAAGCTACA | 16924 |
| rs29629987 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74696803 | ACAACATGAGATGTA[G/T]TAAAGGGTTGATGTA | 16924 |
| rs29630350 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Lnx1 | Mm_Celera | 5:74690545 | TACCCTCCATTAGAC[C/T]TTTACATCTAGGGAA | 16924 |
| rs29631617 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Lnx1 | Mm_Celera | 5:74642165 | TTCCAATGGCTGCTT[C/T]AATATGTTCTTTTAC | 16924 |
| rs29633942 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648010 | ATCCTTTGTGAGCTC[A/C]CATCCACTTTCTGGA | 16924 |
| rs29636644 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Lnx1, Fip1l1 | Mm_Celera | 5:74598908 | ACTCAAGTGGCTGGG[C/T]TCACCTATGAGGGAT | 16924 |
| rs29637979 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74626682 | AGCCACCTCCACCCA[C/T]ACACTATAAATAAAT | 16924 |
| rs29668312 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74642747 | GCTGAGGCAGGAGGA[C/T]AATAGGTTCTGCGTT | 16924 |
| rs29669864 | snp | C/G | 0.487535 | 0.077957 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679246 | CAATCTCTTCTTACA[C/G]ATGCTCACCCTAGAG | 16924 |
| rs29675747 | snp | A/C | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74619009 | CAAACACCCCCCCCC[A/C]AAAAAAAAAACCTCC | 16924 |
| rs29676660 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74675850 | GTGGGTGTGGTCTTA[C/T]ATCCTGATTTCAAGT | 16924 |
| rs29678941 | snp | C/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74603303 | GACTGAAGAAGGCAC[C/G]GTTCCCTTTGTATAT | 16924 |
| rs29680820 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74610307 | GCAGGTTGGGAAACC[A/G]AAAAAAAAAACAAAT | 16924 |
| rs29682304 | snp | A/C | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698667 | TGTTATATATGTGGA[A/C]TAATGCTCACTTTCA | 16924 |
| rs29684846 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650706 | AGAGCATGGAACTCC[C/T]CAATGCTCAGGGCAT | 16924 |
| rs29728436 | snp | A/C | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74682202 | GGTAACAGATGTGCG[A/C]CCCTGCCCTTGGTTG | 16924 |
| rs29728920 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74669085 | AAGCTAAACATCGAG[A/G]CAAGTGTGGCCCTAG | 16924 |
| rs29730500 | snp | C/T | 0.432133 | 0.171253 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74678836 | AATCTCACCGAGGCC[C/T]GAATTGAACTTGACT | 16924 |
| rs29730868 | snp | A/T | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74665160 | AGCGGTGTGAGGGAG[A/T]CTGTTCCCACAAGCC | 16924 |
| rs29731028 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648771 | TCTAGCCCATGTGTA[C/T]GTCATGCTCTGAAGT | 16924 |
| rs29731125 | snp | C/G | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74674100 | TGTGTTCTCTTTGGG[C/G]TCTAAGAAGGTCAGA | 16924 |
| rs29731556 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon | Lnx1 | GRCm38.p3 | 5:74620271 | CAGCACCGTTAGCCG[A/C]AGCACCTGGCAGGGC | 16924 |
| rs29733557 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74592233 | ACAGGTTTCCTTCTT[A/G]TCACCTAAACATGAT | 16924 |
| rs29773890 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74612143 | TGAATGTATGTGTCC[C/T]CCATGGGTGGAAATT | 16924 |
| rs29776410 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Lnx1 | Mm_Celera | 5:74694944 | GAATAAGATGTCCTC[C/T]CACATCCGAGCTATA | 16924 |
| rs29778987 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74594692 | TTCTACTGTAGAAGC[C/T]ACTGTGAGCTATATA | 16924 |
| rs29780431 | snp | A/T | 0.188366 | 0.242283 | intron-variant | Lnx1 | Mm_Celera | 5:74675568 | ATCCAACTGGGTCCA[A/T]GCATGGTGGCAATAT | 16924 |
| rs29810466 | snp | C/T | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74608559 | CACTCATAGAAAAGC[C/T]AACCATATAAAATGG | 16924 |
| rs29812219 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679033 | AGAGCATCAGCAACA[A/G]CAAACAGTATTCTAA | 16924 |
| rs29817977 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74642855 | TAAATGGCAAAGAGG[A/G]TTGGAGATGTGGCTC | 16924 |
| rs29821863 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Lnx1 | Mm_Celera | 5:74699593 | CCAGAATAATCGAGC[A/G]CCTAGAACCGAACAC | 16924 |
| rs33032651 | snp | A/C | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74691895 | CGGCCCCCCCCCCCC[A/C]CACACACACACACTT | 16924 |
| rs33039339 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675641 | CTAGGTGTGGTACCC[A/G]GTACTGCAGGTAAAC | 16924 |
| rs33054473 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74676790 | AATTTACCCAAGACT[A/G]TTTTAAAGATATACA | 16924 |
| rs33060279 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74688677 | AACTAAGCAGGCCGA[A/G]CTACCAGACTGTCTT | 16924 |
| rs33071651 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Lnx1 | Mm_Celera | 5:74659233 | AGACTGCCTTGGGTC[C/T]AACAGTTTTTAACCG | 16924 |
| rs33071888 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Lnx1 | Mm_Celera | 5:74630689 | TCTGAGGTCAGTGCA[A/C]TGGGGACACTGAGCA | 16924 |
| rs33073763 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638755 | CATGCTGGATGCAGG[A/G]AATGGTAGGTTCCAT | 16924 |
| rs33076299 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74647925 | TGGGATGGTGCTGGG[A/G]GAGGGGCGGGGTGTG | 16924 |
| rs33082958 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Lnx1 | GRCm38.p3 | 5:74632622 | TCCGTAGCATCCTCA[A/G]TGTGATGAAATGTGG | 16924 |
| rs33094159 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74598296 | CATTCTCAGAATTAG[C/T]GATTAATTGCAAGGA | 16924 |
| rs33095986 | snp | A/T | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74627797 | ACATATCTCACTATT[A/T]AAAAAAAAAAAAATC | 16924 |
| rs33099056 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Lnx1 | GRCm38.p3 | 5:74676233 | AATGACTTGCCTCAA[A/G]TGTCTTTTTCTATTT | 16924 |
| rs33103488 | snp | C/G | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74622398 | GTGCCACATCCCAGC[C/G]ACCAGTGGGAATGTC | 16924 |
| rs33107628 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682205 | AACAGATGTGCGACC[C/T]TGCCCTTGGTTGATA | 16924 |
| rs33109364 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682208 | AGATGTGCGACCCTG[C/T]CCTTGGTTGATATGG | 16924 |
| rs33110068 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638568 | GGGAGCTCAGAGCAG[A/G]AGAGCACACACCCTG | 16924 |
| rs33117899 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Lnx1 | Mm_Celera | 5:74610470 | TGGAGTTAAACACTG[A/C]CCAGCGCCTTCCTCC | 16924 |
| rs33117903 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Lnx1 | Mm_Celera | 5:74700322 | GATTCAAGGTCATTG[A/G]TGGGTACAACATATT | 16924 |
| rs33118660 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74619675 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 16924 |
| rs33141836 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653672 | AACTACTTAATTTAA[A/G]TTTGCTCTAGACAGT | 16924 |
| rs33156005 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675845 | TGACAGTGGGTGTGG[A/T]CTTACATCCTGATTT | 16924 |
| rs33158538 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653660 | TTCTCTTAAGTAAAC[C/T]ACTTAATTTAAATTT | 16924 |
| rs33165126 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638938 | TCTTGGGGCTGGAGA[C/T]AGTAGGCACAGAGAA | 16924 |
| rs33176412 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682114 | TAGGTAGCCCATATC[C/T]GCGTTGAACTCCCTA | 16924 |
| rs33177695 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675117 | TCAAGGTCCAGCTCA[C/T]ACCCCAAAGTTCTCT | 16924 |
| rs33178447 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74630246 | CCGGGGCTTGGACTC[A/G]AAGGTTGAGTGTTCT | 16924 |
| rs33178608 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638905 | CACTCCCGGGGGCTC[A/G]GCAAAGCTAAGCTAT | 16924 |
| rs33179245 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Lnx1 | Mm_Celera | 5:74643175 | GGGCACCCAGATGTC[A/G]GCAGGAGTCTTTTTT | 16924 |
| rs33188679 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74676049 | CCATCAGGAGGGGAG[A/G]GGAAGCTCTGCCACT | 16924 |
| rs33189772 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74668286 | TGGCTTCAGAGGCCA[C/T]ACTTTCTTCTTTGCC | 16924 |
| rs33196001 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701835 | TGATAAGAAGACAGG[C/T]TGGGGACTTGTTTCT | 16924 |
| rs33199431 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74642600 | GGGTAGGGAAGGAGG[C/G]CAGCTTTTTGCCCAA | 16924 |
| rs33202483 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Lnx1 | Mm_Celera | 5:74659406 | ATGTTCTTCTAGCAT[C/T]CTTTCCATCCACCTC | 16924 |
| rs33209709 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74678621 | GAAGAGGAGGAAGAG[A/G]AGTACAGGAGGGTCT | 16924 |
| rs33212427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74692969 | TGGTCCCCGAGGTGT[A/G]GATCATCCCATCCTC | 16924 |
| rs33218126 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74676710 | ATCCTAGTCATGTAG[C/G]AAAGTATATTTATAT | 16924 |
| rs33222339 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679137 | AGCGGCTCGTCTATC[C/T]TTGTCTCATTTTTTT | 16924 |
| rs33238632 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74605884 | CCCTAAGATTTCTAT[A/G]GGGATTTTCATTTGC | 16924 |
| rs33239390 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74621210 | TGTGTGTGTGGGGGG[A/G]GAGAGAGAGCGAGAG | 16924 |
| rs33248363 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638930 | AGCTATACTCTTGGG[A/G]CTGGAGACAGTAGGC | 16924 |
| rs33252236 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Lnx1 | Mm_Celera | 5:74660887 | ACATCAAAGGAGACA[C/T]GGTGATTTACAGCAA | 16924 |
| rs33252616 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74668566 | ATGCCCAGGAAGTCA[A/G]ACTCCAACTGAGGAT | 16924 |
| rs33255136 | snp | A/G | 0.465374 | 0.126941 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74678807 | TTCTGATAGAGTCTG[A/G]CATACTCATGGCTAA | 16924 |
| rs33256913 | snp | G/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Lnx1, Fip1l1 | Mm_Celera | 5:74598909 | CTCAAGTGGCTGGGT[G/T]CACCTATGAGGGATT | 16924 |
| rs33257278 | snp | A/C | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74624678 | AGACAGTCCTTTATG[A/C]ATGTGTGTGTGTGTG | 16924 |
| rs33259882 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74606932 | TTGTTGTTGTTATTT[A/G]TTTTTTTGTCTTGCT | 16924 |
| rs33271858 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74644668 | TTTTTTTTTTCAATT[A/C/T]TTTGAGGGATTCCAT | 16924 |
| rs33274298 | snp | A/T | 0.432133 | 0.171253 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679234 | CAAGTTCTGGTACAA[A/T]CTCTTCTTACACATG | 16924 |
| rs33274404 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682365 | ACAATAAGAGTGGTC[A/G]AAAATGCTAAATTGT | 16924 |
| rs33274443 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74666393 | TGCTGGCTATTCACA[C/T]CACTCAGGGAAGGCA | 16924 |
| rs33299342 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Lnx1 | Mm_Celera | 5:74680014 | CCATGCCCTGGTGCA[C/T]TACTGCCTGTCCTCT | 16924 |
| rs33309541 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648934 | TTTGTGTCAGAATTT[A/G]GGCTAGAGAACGTCT | 16924 |
| rs33314454 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Fip1l1, Lnx1 | GRCm38.p3 | 5:74594937 | TCACTGCCTTCTTAA[G/T]TTAGGTGTGACACTG | 16924 |
| rs33317406 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675640 | CCTAGGTGTGGTACC[C/T]AGTACTGCAGGTAAA | 16924 |
| rs33327066 | snp | G/T | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74676432 | ACCCTGGACATCCCA[G/T]CACCTAGGCAACTGA | 16924 |
| rs33327912 | snp | A/C | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74647695 | GCTGCAAGGCCAGCC[A/C]TGTTATGACTTTGAC | 16924 |
| rs33331652 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74680616 | TCCTCCCCAACTTGC[A/T]TCTTGGTCATGATGT | 16924 |
| rs33338027 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74665157 | GAAAGCGGTGTGAGG[A/G]AGTCTGTTCCCACAA | 16924 |
| rs33344497 | snp | C/T | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74641755 | ACCTGTCAGGCAAGC[C/T]TGATCAATCTCTCTT | 16924 |
| rs33351512 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Lnx1 | Mm_Celera | 5:74659953 | AAAAATCATTCCCAA[A/G]CATAGAACCCAGAAC | 16924 |
| rs33356043 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697546 | ATAAGTTACAATGCA[A/G]ATGTCTTTAGAGGTG | 16924 |
| rs33360328 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Lnx1 | Mm_Celera | 5:74642099 | AGATGCTTCCGAGTG[C/T]ATGCTCGCTTGGATG | 16924 |
| rs33364324 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Lnx1 | GRCm38.p3 | 5:74668311 | TTTGCCTTTTCAAAA[C/T]GCTTTTTATTAGTGC | 16924 |
| rs33376246 | snp | A/T | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650701 | TGTGCAGAGCATGGA[A/T]CTCCCCAATGCTCAG | 16924 |
| rs33378457 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74639208 | AGCCCAGGCTAGTCT[A/G]GAACGTGAGATCCTC | 16924 |
| rs33380661 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Lnx1 | Mm_Celera | 5:74694575 | CTGCGAATGACATTC[A/G]CCTGCAAAGTGTTCC | 16924 |
| rs33380925 | snp | C/T | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74604655 | GCCCAAGCTCACCAG[C/T]GTTTTGCAGAAACAA | 16924 |
| rs33383525 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Lnx1 | Mm_Celera | 5:74642207 | CAGCTCTACATTGTA[A/T]GCAATTCCAGTACTT | 16924 |
| rs33388593 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Lnx1 | GRCm38.p3 | 5:74677054 | TTCTCTCTTACTGAC[A/T]TTGCACCTGTTTTCA | 16924 |
| rs33394092 | snp | A/C | 0.207612 | 0.24638 | synonymous-codon, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74595965 | AGAACAGGAGAGCAC[A/C]GAAGCCGCCCCTGCC | 16924 |
| rs33403325 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701834 | TTGATAAGAAGACAG[A/G]CTGGGGACTTGTTTC | 16924 |
| rs33406700 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682423 | CCAACACTGAGGAGA[C/T]GGGGGCAGGAAGGTC | 16924 |
| rs33409027 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682698 | GGGTCTTCCTAATGT[C/T]CCTTTTAAGAGAAGG | 16924 |
| rs33412561 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675459 | ACCTAAAGTTAACTC[C/T]ACTCAGAATTGTGAA | 16924 |
| rs33414711 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Lnx1 | Mm_Celera | 5:74696931 | GAGTTAAAAAGCTGC[C/T]CTACTCACGGACACA | 16924 |
| rs33418527 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74634666 | CAGATGTGGGGTGGC[A/G]CACCCACCCTTAGTC | 16924 |
| rs33432806 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698479 | CCATCATCATCTGTC[C/T]ATCCGTCTACCATCC | 16924 |
| rs33434311 | snp | A/C | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74618973 | AACAAAAAAACCCCC[A/C]AAAACAGAAAAACAA | 16924 |
| rs33438310 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675882 | TGTGGACTCCAAAAC[A/G]GTGAAAAAATAAGTA | 16924 |
| rs33452389 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611626 | TTATTGGAAAGGTTC[A/G]TTCCCCATGGTAAAT | 16924 |
| rs33455208 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74704134 | CCTTCTCCCTGAGTG[C/T]CCACATTGGTAGCTG | 16924 |
| rs33458713 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74665265 | GAAAAAAAAACCCAA[A/G]CCCAAAACCCAAAAT | 16924 |
| rs33460381 | snp | C/G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74704265 | ACAGGCCTAAACAGC[C/G/T]CATCCATCTGGGACC | 16924 |
| rs33481354 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Lnx1 | GRCm38.p3 | 5:74639282 | CACATCCAGCGTTTC[C/T]CGTTTGAATGACTGT | 16924 |
| rs33481819 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638967 | AAGTCTGATGCTAAG[A/T]CTGGAGAGGGAGAGG | 16924 |
| rs33487417 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74678789 | TAGATCAGACATAGG[C/T]ATTTCTGATAGAGTC | 16924 |
| rs33489284 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | GRCm38.p3 | 5:74668868 | CTAAATAGCTACAGT[A/G]CTGGGCCACAGGTGT | 16924 |
| rs33492150 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74615424 | CATCCAGCACATGCT[A/G]CCAAAGCCCTGGGCA | 16924 |
| rs33500478 | snp | G/T | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74641853 | TAGCAGTCCCTGTTT[G/T]CCCGGGACTAACCTG | 16924 |
| rs33502033 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682546 | GAGCAAAACGTCTTC[A/G]CAAAAGCTCTCCCCA | 16924 |
| rs33511591 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74667742 | GAGCACCTTGAAGCC[A/G]CCCTCTTGATCATTT | 16924 |
| rs33511929 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Lnx1 | Mm_Celera | 5:74682810 | ACTTTTACAAACACA[G/T]ATTTGGGTCTGGTGC | 16924 |
| rs33524428 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74595239 | GTAGTGACCCGGCTC[C/T]AAATAGCTAACTGTA | 16924 |
| rs33528724 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Lnx1 | Mm_Celera | 5:74644278 | AGCGTATGCTGCCCA[C/T]AAACTCTTGCTTCCA | 16924 |
| rs33537925 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Lnx1 | Mm_Celera | 5:74690265 | CGAGGAGATTCTATA[A/G]TACTCAAGGAATTGA | 16924 |
| rs33544172 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Lnx1 | Mm_Celera | 5:74633532 | TAATTATCGCTCCTG[A/C]AGTGACTAATACTGG | 16924 |
| rs33544767 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Lnx1 | Mm_Celera | 5:74643942 | TTTGGAATCTATGGA[A/G]TCTAAGCATACTCGA | 16924 |
| rs33552454 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Lnx1 | GRCm38.p3 | 5:74699988 | AAGAGGCACTGCCTG[C/T]CCCTGATCTCCATTA | 16924 |
| rs33554641 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74666741 | AAGGCTGTGTCTGCT[C/T]AGTTCCCTGCTGTCC | 16924 |
| rs33557993 | snp | C/T | 0.415225 | 0.187619 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656063 | GTGAGTCACCCAGAG[C/T]AGAAAGGTCAGAGCT | 16924 |
| rs33558229 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Lnx1 | Mm_Celera | 5:74628262 | AGAAACCTCTGGGGA[A/G]AGCGTCGTTGCCATG | 16924 |
| rs33562630 | snp | C/T | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74609899 | AAACTGGGCTGAGTC[C/T]CCTGGAGCCACCAAG | 16924 |
| rs33565299 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Lnx1 | GRCm38.p3 | 5:74612108 | AGCTGTCTGATGCTT[A/G]CCTTTTGCTGACAAT | 16924 |
| rs33568726 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Lnx1 | GRCm38.p3 | 5:74677228 | ACACACGGACACACA[C/T]CAAGCAGCTTAGCAC | 16924 |
| rs33581483 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Lnx1 | GRCm38.p3 | 5:74615560 | ACAACATACTGTCAT[G/T]CTGTCAATCAACTCA | 16924 |
| rs33581526 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Lnx1 | Mm_Celera | 5:74610895 | TTTATTTAATGGAAA[A/G]TCAAGTCCCTAAATT | 16924 |
| rs33598325 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74615191 | TGACCCTGACTGCAC[A/G]TTTGTACATGTGTTT | 16924 |
| rs33603294 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653700 | AGTCTTTACTGTCCC[C/T]AATAATGCCAAGATT | 16924 |
| rs33610523 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Lnx1 | GRCm38.p3 | 5:74641994 | GGGATGCTCTTACCA[A/G]TGACAGTAGTACATA | 16924 |
| rs33611830 | snp | G/T | 0.375 | 0.216506 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648946 | TTTGGGCTAGAGAAC[G/T]TCTACATGTTGATGT | 16924 |
| rs33618418 | snp | G/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74655138 | GCTGTTGACCCTCTA[G/T]GTGGCCAGGGAAACC | 16924 |
| rs33637879 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698726 | GCACCACGCACACAC[A/G]CACACACACACACAC | 16924 |
| rs33650209 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Lnx1 | GRCm38.p3 | 5:74639283 | ACATCCAGCGTTTCC[C/T]GTTTGAATGACTGTC | 16924 |
| rs33664552 | snp | C/T | 0.475309 | 0.108333 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74647747 | CTTGTCAACAAAGTT[C/T]ACTGGCCATCATCAA | 16924 |
| rs33669953 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74615197 | TGACTGCACATTTGT[A/G]CATGTGTTTTTGCAC | 16924 |
| rs33671363 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74642925 | AATTCTTAATATTGT[A/G]GCATGCACAAGCATG | 16924 |
| rs33673445 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74676551 | GTCTGGTTACCATGG[A/G]GGAATTTTGTAAATA | 16924 |
| rs33674381 | snp | C/T | 0.359862 | 0.224567 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656111 | CTGCCATTTATGTCT[C/T]CAGAGCTGTGGCAGC | 16924 |
| rs33675791 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Lnx1 | Mm_Celera | 5:74661802 | TAGGCCTACAAGTTA[C/T]TGCAGTATAAATAAA | 16924 |
| rs33679529 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611591 | CTTGGGCAGAAGATT[C/T]GGAATAACAAATGTA | 16924 |
| rs33683566 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74626777 | TTTCAGAGGTCCTGA[A/G]TTCAATTCCCAGCAA | 16924 |
| rs33697494 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Lnx1 | Mm_Celera | 5:74674499 | CTTGGGATTAAATTA[C/G]TTTTAAATTAAATTT | 16924 |
| rs33698418 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682364 | GACAATAAGAGTGGT[C/T]AAAAATGCTAAATTG | 16924 |
| rs33701652 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74674655 | CTTGTAGGTGTGAGT[C/T]GGGACAGACAGTCCT | 16924 |
| rs33706463 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Lnx1 | GRCm38.p3 | 5:74639375 | TCAGCCCTCACTGGC[A/G]TGTGCAATGTGCAGG | 16924 |
| rs33706871 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Lnx1 | Mm_Celera | 5:74672319 | GGGAAGAAATAGATG[A/C]TGAAGTCATTCCTCT | 16924 |
| rs33711393 | snp | G/T | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74622702 | ATGCCTCAGAGGACA[G/T]TATGCCCAAGCCAGG | 16924 |
| rs33721605 | snp | A/C | 0.304688 | 0.243945 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679136 | CAGCGGCTCGTCTAT[A/C]CTTGTCTCATTTTTT | 16924 |
| rs33727035 | snp | A/T | 0.456747 | 0.140554 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74655435 | ATCCCACAGCAGAAG[A/T]GCATCAGGACCAAAA | 16924 |
| rs33732750 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Lnx1 | Mm_Celera | 5:74667599 | CTTTATTAATGCCTG[A/G]TCCTGACATTTCTTT | 16924 |
| rs33733760 | snp | G/T | 0.33241 | 0.236027 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74657313 | GTGTATAAGGGGAAT[G/T]AACCAGGGACATGAG | 16924 |
| rs33742246 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74610654 | CCTTGCAGGAGCTGC[C/T]GACATGCCTGGCTGG | 16924 |
| rs33747947 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653708 | CTGTCCCTAATAATG[C/T]CAAGATTGTATAACT | 16924 |
| rs33749518 | snp | A/C | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74618972 | AAACAAAAAAACCCC[A/C]AAAAACAGAAAAACA | 16924 |
| rs33749553 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | GRCm38.p3 | 5:74647336 | GAGTTAGGGAGTGGC[C/T]CAGGCATTAAGCTGT | 16924 |
| rs33753182 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | GRCm38.p3 | 5:74605390 | CAGACAACAATCTAA[A/G]GGCCAGTAGATTTTG | 16924 |
| rs33755289 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lnx1 | Mm_Celera | 5:74668394 | GGACAACAAACTGGT[A/G]CTTGTAGTTTGCCAC | 16924 |
| rs33760641 | snp | C/T | 0.387812 | 0.208586 | intron-variant, utr-variant-5-prime | Lnx1 | Mm_Celera | 5:74660424 | CTATGATTGAATGAG[C/T]CTTCAGATGCACAGG | 16924 |
| rs33892655 | snp | A/G | 0.5 | 0 | synonymous-codon | Lnx1 | GRCm38.p3 | 5:74620007 | ACTCTCTGGACTGCC[A/G]AATCGAAGGTCATGC | 16924 |
| rs33892719 | snp | A/C | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74619852 | CTCGTTCATTGAAAA[A/C]TCCAGCCCTTGCCCT | 16924 |
| rs33893462 | snp | G/T | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74619853 | TCGTTCATTGAAAAA[G/T]CCAGCCCTTGCCCTG | 16924 |
| rs45635391 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74615506 | GCCAGACATCATCAA[A/G]CCTACATTTTTCTCT | 16924 |
| rs45638979 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74671362 | AAGTTCTTTATTTTC[A/T]TTTTTCCTTTTGCTG | 16924 |
| rs45644904 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701714 | TGGATGATTTCCTTA[C/T]AAACCCCGCTGCTAA | 16924 |
| rs45650744 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74639351 | ACTCGTGCTTACCCT[A/G]ATCACCACTCAGCCC | 16924 |
| rs45661770 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694809 | AGAGGCCTGGGGATG[A/G]CTTTTCACAGCCTTC | 16924 |
| rs45665086 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74640136 | AGCTCATCTTAAAGA[A/G]CCAACAGGCTTCCCC | 16924 |
| rs45671092 | snp | A/G | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648665 | CCGAGTGCTGGGATT[A/G]CAGGTGTGTGTCACC | 16924 |
| rs45673529 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74616952 | ACACTTGGATGTAAT[A/G]TACAGCGCCGCCTAA | 16924 |
| rs45673634 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650578 | TGGAGAATCATTTCC[A/G]GTGCCTCCAGAATCT | 16924 |
| rs45677884 | snp | A/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74644809 | CTGTCACCAGAAACT[A/T]CAGTGAAATCAATGG | 16924 |
| rs45688763 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74686822 | GTTTAAGCCAAGGGC[A/G]CATTGAGCCTCCCGT | 16924 |
| rs45693968 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74605224 | AATCCAGACCAGTTT[C/G]TATTTGAGGCTACTA | 16924 |
| rs45700065 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604784 | TCTACTCCCTCTGCT[C/T]TGGTACCTCTGACCT | 16924 |
| rs45702826 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611484 | CAGCAGTGAACAGAG[A/G]GAAGCAAGGTGAGAG | 16924 |
| rs45703097 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74673716 | AGGAGGTCACAGACA[C/T]ACCAAGCATAGAGGT | 16924 |
| rs45705740 | snp | C/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703344 | TAGCCATATCTGGGA[C/T]TTGTCCCCACTAACG | 16924 |
| rs45706637 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74702629 | CATGGAGTAAGACTG[A/G]CGCAGACATCTCTAC | 16924 |
| rs45714920 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656984 | GAATCAACTTATTAT[C/T]CTGACACGAATTTGA | 16924 |
| rs45718559 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Lnx1 | Mm_Celera | 5:74645020 | AACATAGCCGGAGAT[G/T]CAGGGCTTCCCAAGA | 16924 |
| rs45720854 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651886 | CAGCCAAGACCAGGA[A/G]AAAACACTTTATATT | 16924 |
| rs45726576 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74682690 | TAACTACTGGGTCTT[C/T]CTAATGTTCCTTTTA | 16924 |
| rs45727409 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74641020 | GCCAAGCGTAGCCTG[C/T]TCTCATCAAGCCAGT | 16924 |
| rs45740973 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74684457 | CTATAAGAGAGAACA[C/T]TGAACAAGCCAGGAA | 16924 |
| rs45749128 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651239 | AACCTGAAACACCAA[C/T]GAGCTTACACTATCT | 16924 |
| rs45752902 | snp | G/T | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646744 | AAGGAAGGAGTCACG[G/T]AGTACACATGTGGAG | 16924 |
| rs45772385 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74673608 | ACCCCATTCAGTTTC[A/G]GTCCTCGCGCTTCAG | 16924 |
| rs45795387 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon | Lnx1 | GRCm38.p3 | 5:74685722 | TGGGGAGTGGTTTTG[C/G]CCACACACTATGCAC | 16924 |
| rs45797451 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Lnx1 | Mm_Celera | 5:74685584 | CAGGAAGTTGGTGAG[A/G]CACAGGGTGCAGTAG | 16924 |
| rs45806346 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74667741 | AGAGCACCTTGAAGC[C/T]GCCCTCTTGATCATT | 16924 |
| rs45808291 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697359 | TATATATCCCCTAGA[C/G]GTGAACCCTACAGAG | 16924 |
| rs45818583 | snp | A/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74640476 | TGAGATACGGTTGGC[A/T]AGTCTCTGAACGGGG | 16924 |
| rs45819809 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74686679 | CAACTCTAAGCCAGG[C/T]TGTGAGCCGACAGGG | 16924 |
| rs45823523 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74602812 | CTTGGCTTTCTGCTC[C/T]GTTGCATTGCATCTC | 16924 |
| rs45857915 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74690524 | ACTTTGCAAAACAAA[C/T]CATTCTACCCTCCAT | 16924 |
| rs45868291 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74670763 | AACTTACAATCTCTA[A/T]TAGTCTAGCATTTGT | 16924 |
| rs45868479 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698061 | GCAGCACATGTTTGA[A/G]GTGCACTGGTCAACC | 16924 |
| rs45874208 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74691331 | GACAGATGGAGATAA[A/G]ACCTAGGGTTATAAG | 16924 |
| rs45877420 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74662619 | GGGACAAATATTGAA[A/G]TAGAAATTTATCTCC | 16924 |
| rs45882216 | snp | C/T | 0.124444 | 0.216185 | missense | Lnx1 | Mm_Celera | 5:74685733 | TTTGCCCACACACTA[C/T]GCACAGAGGCTCGGG | 16924 |
| rs45884955 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74633364 | TAGCCAGGGAGGTTG[A/C]AGAATCTACAATGCA | 16924 |
| rs45885700 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74612596 | ACAGATACATGCAGA[C/T]ACCACGCACACAAAG | 16924 |
| rs45893938 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Lnx1 | GRCm38.p3 | 5:74636942 | GGAACCCCTATGACC[A/G]AATGGCTGATGGCCT | 16924 |
| rs45902800 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654143 | CACTCCGTTCCATCA[C/T]AACACTCTGGAGTTC | 16924 |
| rs45904184 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Lnx1 | Mm_Celera | 5:74696958 | CACAGCCATGGTTCT[C/T]CCCAGATCTAGGAAG | 16924 |
| rs45906654 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74605573 | AGAGATGTTGTGAGA[A/G]GCATCCCCAGCTAGC | 16924 |
| rs45912355 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74680718 | TCACTGTGAGAAGGT[A/G]TGCCAGTGTGTGGAT | 16924 |
| rs45919771 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683609 | GGACAGGACCTACCT[C/T]ACCTTTGACCTTGAG | 16924 |
| rs45923216 | snp | C/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74613705 | GGGCTAGAATTGCTT[C/G]TCTTGGACAGTGAGC | 16924 |
| rs45923236 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74614281 | TAATGGGAAACAGTG[A/G]CTAGGAGGGCAATGA | 16924 |
| rs45933791 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697433 | ATTCTAAGTGACAGG[A/G]TAAACATTTTGGGAT | 16924 |
| rs45935048 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74674929 | CTCTTTATCTCAAGG[A/G]CACACAGCCACCTCC | 16924 |
| rs45946822 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681201 | GGGCAGAGAGTTGGT[C/T]CTATGAAGCAACACT | 16924 |
| rs45966239 | snp | C/G | | | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593392 | TCAGAAGGGATGGGG[C/G]GCGGCTGCTGTTTTC | 16924 |
| rs45988311 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Lnx1 | GRCm38.p3 | 5:74640941 | AGCTCTTGGGTATAT[C/T]CTATTCTTTACTACT | 16924 |
| rs45999234 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74682539 | AAAAAAAGAGCAAAA[C/T]GTCTTCGCAAAAGCT | 16924 |
| rs46007020 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74644567 | CTGTGACCTGGATTC[A/G]TTCTTAAACGTGGTC | 16924 |
| rs46011105 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74595311 | TCCTTCCTTAGGAGC[A/T]TCAAAAACAGTTTTT | 16924 |
| rs46014121 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650941 | TGCACCTGTTCTCTT[C/T]TCAAATTCTTTTAGC | 16924 |
| rs46049868 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74662666 | AATTCTTTAGAAGTA[A/C]ACATAGAGAAATCAG | 16924 |
| rs46052494 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74641234 | AGCTTTGGCCTCCTC[A/G]TCCTAGAAGCAGAAG | 16924 |
| rs46055774 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74613570 | AGTAAAAACTCACCG[A/G]GAGATAAGTAGCAAT | 16924 |
| rs46057592 | snp | A/C | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74704985 | AAGAGAAACTCCTGG[A/C]TATTTTATATGGTTA | 16924 |
| rs46060279 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694488 | TGCTGCGAGGATTGC[A/G]GTTAGATCTGGTTCT | 16924 |
| rs46075450 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697801 | CATCACCTCAACAGA[C/T]AGCAATGACATAGCT | 16924 |
| rs46077433 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74613263 | CCATCTAGGAAATGC[A/T]ACTGAATGGCCCAAC | 16924 |
| rs46082888 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74616986 | ATTCTCATGAAATGT[G/T]ATACGGGCTTCCAAG | 16924 |
| rs46084262 | snp | G/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74601571 | TAAATACTTTTATCA[G/T]GATATCTTGCTCTCT | 16924 |
| rs46090594 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74660856 | TTACAGTCTAGTCAA[C/T]GGGCAGTCAAATGCT | 16924 |
| rs46095739 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74695647 | ATGAGGCCCTGTCTT[A/T]AAAAAAAATTAACAA | 16924 |
| rs46095894 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74614786 | AGTCTAGGTCTGCAA[A/G]AGAGGCGTATTTGAA | 16924 |
| rs46111775 | snp | A/C | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74612082 | ATATGTCCATTAGCT[A/C]AGGCAGTAGCAGCTG | 16924 |
| rs46113445 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74636796 | TGACATGGTTTGAAT[A/G]TATCCCTCAAGGGTT | 16924 |
| rs46129246 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74666042 | ATGCAAGGATGCCCA[A/G]CTTCTCAAGTGGCTG | 16924 |
| rs46131878 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74630741 | TTGCCTGGGCATGGC[A/G]GACACCATGGCAGAA | 16924 |
| rs46149523 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74641338 | TTAGTTCCAGACTTT[A/T]TTTTCTCTTGCATGC | 16924 |
| rs46152952 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Lnx1 | Mm_Celera | 5:74613568 | CAAGTAAAAACTCAC[C/G]GGGAGATAAGTAGCA | 16924 |
| rs46153407 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604693 | CTGACATTGCTTTTC[A/G]CTGGACACATGCTCA | 16924 |
| rs46155066 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74685080 | CCCGACATTCATAAC[A/G]CCATTTTTTTTTCCG | 16924 |
| rs46155419 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74695070 | AGAGCTAACTCTAGG[A/G]AAGTATGGGAGCGAA | 16924 |
| rs46160351 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74663103 | CATTGGCTCACACCC[A/C]CAACACGCCTAGGGG | 16924 |
| rs46165797 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74665348 | ACAGTGTTCTTCCTC[A/G]TCTCCTTCACCTCTC | 16924 |
| rs46179973 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74660654 | AGGAGGAGTGAGCCA[A/G]ACAGCTGATAAACAT | 16924 |
| rs46216432 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lnx1 | Mm_Celera | 5:74645201 | TTGACATAAATTAAG[A/G]AAGGATCGCTACAGA | 16924 |
| rs46219601 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74671266 | GATAATCATGTCTAA[A/G]ATTTGCTGCCAACAA | 16924 |
| rs46239762 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596634 | AAGGATCAAGGTGCT[C/T]TGGCTGCTGTTAGTA | 16924 |
| rs46243658 | snp | C/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74670517 | GCTAACTATAATCAA[C/G]AGTCATATAAATATA | 16924 |
| rs46252868 | snp | A/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703857 | AGCCTGTTGAATTGC[A/T]GTGTGTCTGTGGCTC | 16924 |
| rs46264703 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74671352 | AGGGACCCAGAAGTT[C/T]TTTATTTTCTTTTTT | 16924 |
| rs46275029 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Lnx1 | GRCm38.p3 | 5:74670520 | AACTATAATCAACAG[G/T]CATATAAATATATTC | 16924 |
| rs46278764 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74695449 | GTCAGGCCCAGGAAA[C/T]TTAATGGACCACCTA | 16924 |
| rs46281766 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74695989 | TGATTTTGGGTTGAG[C/G]AAAGATCATAGGTTC | 16924 |
| rs46285776 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | GRCm38.p3 | 5:74613276 | GCAACTGAATGGCCC[A/G]ACAGAGGAAGCCTGA | 16924 |
| rs46291070 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74601456 | AGAGAGCTCATCCAA[A/C]CCAGGTGGGATATAA | 16924 |
| rs46291648 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74602628 | TGATGACTGGCGTAA[C/T]TGGCAGAACGTCTAG | 16924 |
| rs46310289 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654075 | TCCAGCCACAATGAG[C/T]GCTCAGAGTTCTAAG | 16924 |
| rs46332483 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74684969 | CTTCCAGCTAGGCTC[C/T]ATCTCTTGAAGCTCC | 16924 |
| rs46332587 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652925 | TAGGGCTATGCTATA[A/G]GCCCATTAGTTATGG | 16924 |
| rs46342722 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74693611 | CTCTGTCCTTCATAT[A/T]CACGTGTGAACCCAC | 16924 |
| rs46343069 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596987 | CTCTACCACATTTGG[A/G]ACTGACTTGAATTAA | 16924 |
| rs46358661 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593853 | TTCCCCACTGATGTC[C/G]TTTCAGGGCAAGAAT | 16924 |
| rs46362098 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74644121 | AAACTGGTCAGCCTA[A/G]TCCTTGTTCAAAAAC | 16924 |
| rs46369091 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74695598 | TAAAGATCATCCTCA[C/T]CTTTATAGGGAGTTC | 16924 |
| rs46371193 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74612496 | AGTGGATGGTGAGGA[C/G]TGAGTCTCCAGGCTG | 16924 |
| rs46376914 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74693030 | AAGTGTCTATCACTG[C/T]ATCAGCTCTGTAACA | 16924 |
| rs46385329 | snp | A/G/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74664283 | AGATGGAAGGCAGAC[A/G/T]TTAGCGTTCATGACT | 16924 |
| rs46385644 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74634188 | TCCTCACTACCTCTC[A/T]CCGTTCACTTCTGAT | 16924 |
| rs46387651 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74613351 | TTCCTTTGCTAGCCT[A/C]TCTTGAATTCCCTGG | 16924 |
| rs46388018 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74663004 | GGTGGGTTTAAAAAT[C/T]GAGGGAATAATATTA | 16924 |
| rs46395500 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74643629 | CTCAACATTTTTAAC[A/G]GAAACTTAGTACTCT | 16924 |
| rs46397874 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74694013 | CCCAGTGGACCAGTG[C/T]CAGTAACTGCTTTCC | 16924 |
| rs46407184 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Lnx1 | GRCm38.p3 | 5:74614293 | GTGGCTAGGAGGGCA[A/G]TGATATTACAGGCAG | 16924 |
| rs46408486 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74672146 | ATAAGCAAGAAAATT[A/C]CAGATAACTTCCCCC | 16924 |
| rs46412668 | snp | C/T | 0.32 | 0.24 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593136 | TTGTACTAGGAAATA[C/T]TCATGGGAAGTAAAA | 16924 |
| rs46422552 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74671586 | GGTTTTTTAAGAAGA[A/G]CATTTTATATCAGAC | 16924 |
| rs46423268 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74662861 | TAATTATTTCTGAAA[A/C]ACTGCCTTATACTCA | 16924 |
| rs46433868 | snp | C/G | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703222 | CCCTCCAGGCTCACA[C/G]GAGCCCACACAGCTG | 16924 |
| rs46444924 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646980 | GGCTGTGTATTGGCT[C/T]GTGTTCTCATGCTAA | 16924 |
| rs46446123 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74610453 | TTAGAAGGCTTGCAA[G/T]CTGGAGTTAAACACT | 16924 |
| rs46459457 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74640428 | CCTCAGTAGGCACGC[A/G]TGACTCAGTTTACCC | 16924 |
| rs46460683 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74659558 | GCTCTACCTGTCCCT[G/T]GTCTACACCCTAAGT | 16924 |
| rs46468350 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74679665 | GCTCCCTTCCTGCCC[A/G]AAACTACTAGGAGAT | 16924 |
| rs46470973 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653242 | TAGTTATCAAAACTG[G/T]ACTATGAATCCATTG | 16924 |
| rs46475929 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74668653 | CTGTTAGCCAAAAAA[A/G]TGCTAACAACTCATT | 16924 |
| rs46478687 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74643901 | ATCACATTAAAGTTT[A/T]TTTTTTTAATTTTAT | 16924 |
| rs46483682 | snp | A/T | | | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656733 | GCATCGGATTGTAAC[A/T]TTTTTTTTTGTTTTT | 16924 |
| rs46490482 | snp | A/C | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74640312 | TGAGATGGGGACTTG[A/C]GTTCTAGCTGCCTGG | 16924 |
| rs46493689 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74666178 | ATAGAGGTTGATCCT[C/T]TTTAATCTATCATCA | 16924 |
| rs46496326 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74662548 | TGGGAAGCTCACTTC[C/G]AGTCATAAACAAATT | 16924 |
| rs46504096 | snp | A/C | | | intron-variant, utr-variant-5-prime | Lnx1 | Mm_Celera | 5:74697191 | GGTAAATTCTCTTGC[A/C]GAGCTCCCTCAAAGA | 16924 |
| rs46514083 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74670858 | GTGAGGAGGAGAGGG[A/G]GAAGGAGGAGAAAGA | 16924 |
| rs46516693 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74615963 | AGGATAGTCTCGTCT[C/T]GTTATTTCATGCAAA | 16924 |
| rs46530863 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74661753 | ACACCAAACCCTAAA[C/T]TGAGGGCCACTCCAC | 16924 |
| rs46537042 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74643982 | ATCTGTGAGAGGAAC[C/G]ATATCAAGCATCAGT | 16924 |
| rs46542851 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74613842 | TTGTTTGAGCACACA[C/T]TTCTCACTGGGCTCC | 16924 |
| rs46543889 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683693 | CACTAACACGCACCC[G/T]CACCACCATCTCTTT | 16924 |
| rs46551495 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74640559 | CTGGACCTCTTTTCC[C/T]TTCATGTAAATGGCT | 16924 |
| rs46554386 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703807 | CTAAGAGGATTCCTG[C/T]CTGCTGGTTAAGGCC | 16924 |
| rs46573092 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74693014 | TGAGTGCTGAGGTAA[C/G]AAGTGTCTATCACTG | 16924 |
| rs46583669 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74637138 | TAATGACCTCTGAGA[C/T]GGTGCCCTTCACAGA | 16924 |
| rs46600536 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700534 | AGCATGATGAAAACG[A/G]ACTGGGCTCCCTGAA | 16924 |
| rs46609414 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611882 | GTTAGAAAGGCACCC[A/G]GGGGAAGCCAGGTTC | 16924 |
| rs46611620 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74652156 | TGGAGATTTGACTCA[A/G]CAGTTATCAGTTCCT | 16924 |
| rs46612619 | snp | A/G | 0.231111 | 0.249285 | missense, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74595972 | GAGAGCACCGAAGCC[A/G]CCCCTGCCGAGTAGG | 16924 |
| rs46617005 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700839 | GGTTCTGAACCAGTG[C/T]AGCCACAGGAGAGCT | 16924 |
| rs46633763 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74673093 | GTGAATAGTGAGTGA[C/T]TCCACCTCCAAATCA | 16924 |
| rs46640928 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74659672 | TCCTTCATAAATACC[C/T]GATCTACTCTGTCAG | 16924 |
| rs46645932 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | GRCm38.p3 | 5:74670967 | ACTGGTTATTTGATG[A/G/T]CAAGAAATTATAGGT | 16924 |
| rs46647801 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Lnx1 | Mm_Celera | 5:74685440 | GCGCTGTAGCACCTC[A/G]GTGCAGTGCTCCGTG | 16924 |
| rs46663120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74639613 | CAATATTTCACAAGT[C/T]CTGGAATGGAAAACA | 16924 |
| rs46666244 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74611510 | GAGAGGCAGGAACTC[C/T]GACACTGCAGAAATG | 16924 |
| rs46683412 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74696367 | TTATCCTGGTGTGGG[A/G]AAATCAAGATTCATT | 16924 |
| rs46688952 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701474 | TATTAAGGCATCAAC[A/G]GCAGTCACTCTGCAA | 16924 |
| rs46691415 | snp | A/C/T | 0.473373 | 0.11227 | intron-variant | Lnx1 | GRCm38.p3 | 5:74695730 | GGGGAAAGAGCTTAG[A/C/T]CAAACACTGCCATCC | 16924 |
| rs46694377 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74596234 | AATTAAGTCATCAGG[A/G]GATTTAGAGCTAAGG | 16924 |
| rs46700030 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74661261 | ACTTATCTGCAGAAA[A/G]TAATTCAGCTCTAAT | 16924 |
| rs46700178 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74599624 | CACCTTGGTTGACAT[A/G]TGCCTGTTTTTGGTA | 16924 |
| rs46704547 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Lnx1 | Mm_Celera | 5:74616350 | AGAATAAGCTAATAG[G/T]GTTTGGGAAGTTGAT | 16924 |
| rs46705974 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74652020 | GCAATTATGTAAAGA[C/T]GTTTGTCTTCATACT | 16924 |
| rs46706874 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74636037 | GTTCTCCTTTGCTAG[C/T]GGGATGAGTCAGAGC | 16924 |
| rs46707163 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74671541 | AACCTTGAGTAGAAT[C/T]TTGAAACTGTTGGGT | 16924 |
| rs46711130 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74594517 | GAGACAGGTGCGGGT[A/G]AGGTAGCTGAGATAT | 16924 |
| rs46716144 | snp | G/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74640791 | AGGATCACACAGCTG[G/T]TCCCTGGAGAGGACG | 16924 |
| rs46720502 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654939 | ACAGTGTCAACTGGA[C/T]ATTACCTCCAAAAGG | 16924 |
| rs46728333 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74629169 | CAATCATTTCAGCTC[A/G]CTGACAACGGTCTGG | 16924 |
| rs46748872 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74612781 | TCACCGTCCTCTCTA[A/G]GGCACATAACTCCCT | 16924 |
| rs46765202 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700675 | AGCGACCACTCCAGA[C/G]TCTGCTTCGCCAAGG | 16924 |
| rs46775790 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime | Lnx1 | GRCm38.p3 | 5:74685800 | CATGGCTGTGTAGGG[C/T]TCAGGAAACTCAGGA | 16924 |
| rs46787284 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694466 | AAGGAGGCAGGTACT[C/G]GAAGCCTGCTGCGAG | 16924 |
| rs46789125 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74639856 | CCTGAATACAAGCCC[C/T]CTTCCAGGAACTTTC | 16924 |
| rs46804957 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74692724 | CACCTCATTTTTTGC[A/G]TGGTAGAGACACCAG | 16924 |
| rs46812516 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Lnx1 | Mm_Celera | 5:74697154 | ATACCAAGTGACCTC[A/G]GGACCCAATGGATGA | 16924 |
| rs46831472 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Lnx1 | GRCm38.p3 | 5:74640552 | AGAGGAACTGGACCT[C/T]TTTTCCCTTCATGTA | 16924 |
| rs46831629 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74694147 | TTATAGGGAAAGCAA[A/T]TCCCAGAGTCGAGAT | 16924 |
| rs46855056 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651341 | ATGGTGGCAGAAAGG[A/G]AAAATTCTTCTTCCA | 16924 |
| rs46855192 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74638419 | CTCAAGGTGACAGTG[C/T]GGTTAGTTCACCTCA | 16924 |
| rs46864044 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74684660 | GTGATATTTTTCTGA[C/T]TTTTCTCATGTTAAA | 16924 |
| rs46870176 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74614676 | TCCTCCACCATGCTG[C/T]AGTGTTATTCTCTAC | 16924 |
| rs46872653 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74644141 | TGTTCAAAAACTGCA[C/T]GAAAAATTGAAATAA | 16924 |
| rs46877579 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74690849 | CCCTTGGGCTAGCCT[A/G]GGATGCTTCCTAGCT | 16924 |
| rs46885837 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74695916 | GACCCACAACCCTCC[C/T]TCAGCCTCCTGAGGG | 16924 |
| rs46890564 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74640455 | ACCCAAGATGGTCTG[C/T]ATGCCTGAGATACGG | 16924 |
| rs46891904 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74604875 | AGCCCCTGTCATCTC[A/G]TGTCCTTTCACCCTT | 16924 |
| rs46892094 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74692793 | TAACAAGTGTGGAGC[A/G]ATATTCCCTAAGACA | 16924 |
| rs46897349 | snp | C/T | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74641653 | AAATCCTCTGCATAC[C/T]TGTCTATGACAAAGT | 16924 |
| rs46899778 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | GRCm38.p3 | 5:74672792 | ACTTGGTGGGTGAGC[A/G]GCGTCCCTGTGCCCT | 16924 |
| rs46900149 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Lnx1 | Mm_Celera | 5:74700269 | GGGACCAGAAGAAGC[C/T]CGCAGCGGGTCTGGG | 16924 |
| rs46901484 | snp | A/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74699646 | CACATAAACTCTGCA[A/T]CTGTTTTCCCAGAAA | 16924 |
| rs46903182 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | GRCm38.p3 | 5:74672386 | CAACTGCAGGAATTT[A/G]GATGTACCCGAATGG | 16924 |
| rs46904938 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lnx1 | GRCm38.p3 | 5:74684801 | TAGATCCTACATGAA[C/T]TAGAGAGATGGTTTA | 16924 |
| rs46916480 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1 | GRCm38.p3 | 5:74694065 | TCTCTCTCTCTCTAA[A/G]GAATCTGCCTGGCAG | 16924 |
| rs46919912 | snp | G/T | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant, utr-variant-3-prime | Fip1l1, Lnx1 | Mm_Celera | 5:74597548 | ACGTAAATTCTTCAA[G/T]CTCTACTCGGCTTGC | 16924 |
| rs46920267 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646743 | GAAGGAAGGAGTCAC[A/G]GAGTACACATGTGGA | 16924 |
| rs46925511 | snp | G/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698381 | ACAATTGATTGTACA[G/T]TATGTATTTTCATGC | 16924 |
| rs46932996 | snp | C/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703452 | CTACTTAAAAAAATC[C/T]AATTTTGATACCTTT | 16924 |
| rs46939230 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74672619 | AAGCCCAGAATGCCC[A/G]ACTATATTTGACTGA | 16924 |
| rs46940956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74668765 | AGCCTGTCACTGAGA[A/G]GACTGAGTCACTTGG | 16924 |
| rs46950424 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74680997 | GGGGCTTGAGCCGAC[G/T]GAATCATGTTCTCAT | 16924 |
| rs46952486 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74617295 | TTTCCAGGTATGAAG[C/T]GCAACTCAAGACCTG | 16924 |
| rs46959072 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74647809 | AGACAGTCAGATGCC[A/G]AAACTGCTATTCTGG | 16924 |
| rs46978755 | snp | A/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654006 | CCACATTTGCTGTAC[A/T]CTTGAGCCACGCTGC | 16924 |
| rs46994519 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74636144 | GCCTCTTGCTATGGA[C/T]AAGGTGCTGGTTTAC | 16924 |
| rs47003307 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596938 | AAATCCTCCGCCATT[A/T]AGCTTAAATGCCCAT | 16924 |
| rs47011671 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74629190 | AACGGTCTGGTCAGA[A/T]ACTGGTGATGATTTA | 16924 |
| rs47014353 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74696397 | TTGAGTGATAACCTC[C/T]AAGAATATGGTTTGT | 16924 |
| rs47023824 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74610137 | CTGGATTTGAATGCC[A/G]TAAGACAAGACATGT | 16924 |
| rs47033776 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652942 | CCCATTAGTTATGGA[C/T]CCTCAAGGATGAACA | 16924 |
| rs47040956 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602526 | AGTCCAGATGAGAGC[G/T]TGCTTTGAAGACCTT | 16924 |
| rs47041257 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74697043 | AGATGAGAGCACCTG[A/G]ATTACCCAAGTGATC | 16924 |
| rs47055358 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602508 | GCATATTTCTATCAC[A/G]CTAGTCCAGATGAGA | 16924 |
| rs47058136 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74614343 | CCAGTATATGGCAGT[C/G]CAACCCTCTCATCCA | 16924 |
| rs47064081 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681407 | TGAAGCAAAGACTAG[C/T]AAGGTGGTGTCTATG | 16924 |
| rs47071361 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74605133 | CCTCAATGCTCAGTG[C/T]TTCATTTTCTAAGGT | 16924 |
| rs47080813 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74640514 | CTATTTGAGGGATGG[A/G]GTGAGGAGGAAAAGA | 16924 |
| rs47087203 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74694499 | TTGCGGTTAGATCTG[C/G]TTCTACTTAACTTCT | 16924 |
| rs47104500 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74675072 | AACTGCTCTTGAGAT[A/C]CCATTTGAACCCCAA | 16924 |
| rs47114460 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681388 | ATTGACCTAAGTCTT[C/T]CCTTGAAGCAAAGAC | 16924 |
| rs47116739 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74671551 | AGAATCTTGAAACTG[C/T]TGGGTTTGGATGGAG | 16924 |
| rs47117966 | snp | C/T | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654061 | CGTTTTTCTTGACGT[C/T]CAGCCACAATGAGTG | 16924 |
| rs47127015 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74670039 | AGGGACAATGACTAC[A/G]AAAAAAAGGATGTCT | 16924 |
| rs47134657 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74641363 | GCATGCATAAGGCAG[G/T]GTATTCGCTGTTGAA | 16924 |
| rs47136933 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652902 | GTCTAAATAAATGCT[A/G]CTTATCCTAGGGCTA | 16924 |
| rs47144022 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604051 | AAATCAAAGACTACA[C/G]TGAGGATAGAGCATC | 16924 |
| rs47166084 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | GRCm38.p3 | 5:74616693 | GCGATGAAGGAAATA[C/T]GGCCATGCCGACGTC | 16924 |
| rs47171000 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74598343 | TGCTAATGAACTTCA[C/T]TAAGTTGTAAGCTTT | 16924 |
| rs47171675 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74638421 | CAAGGTGACAGTGTG[A/G]TTAGTTCACCTCAAG | 16924 |
| rs47177428 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74633828 | TCATTTTTCTTAGAA[C/G]TGATGAAGTCGGGTC | 16924 |
| rs47177613 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74697133 | GCAATGTCAAGACTT[A/G]GTCTCATACCAAGTG | 16924 |
| rs47180375 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Lnx1 | Mm_Celera | 5:74604635 | CAAGGCTCCATACCC[C/T]GTATGCCCAAGCTCA | 16924 |
| rs47181776 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74607206 | CATGTGCTTGAACAG[C/T]GTTATTGAGAACACG | 16924 |
| rs47189960 | snp | A/G | 0.18 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74677127 | CACATGTCTGCTTGC[A/G]AGCTATGGTCTTAAT | 16924 |
| rs47192070 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Lnx1 | Mm_Celera | 5:74691561 | TAAATGTATGAACAA[C/T]ATATAATGCAAAAAA | 16924 |
| rs47192694 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74613227 | ATGGACGGCTAGCTC[A/G]GGGAACTGTTCATTC | 16924 |
| rs47196571 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74699748 | CTAGCAATTGTGTGA[C/G]AGATCTGTCTGATCC | 16924 |
| rs47201290 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651870 | ATGAGGCCTATGAAC[A/G]CAGCCAAGACCAGGA | 16924 |
| rs47204416 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74671383 | CCTTTTGCTGTCCAA[A/C]GTTTTCCACCAGAGC | 16924 |
| rs47215675 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648465 | CACAGTGAGTGTTGC[C/T]AACCTAGAACATGTG | 16924 |
| rs47216630 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74664281 | TGAGATGGAAGGCAG[A/G]CGTTAGCGTTCATGA | 16924 |
| rs47219118 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Lnx1, Gm32304 | Mm_Celera | 5:74658362 | ATCCTCTTAATTCTG[C/T]ACCTAATGAGGCATT | 16924 |
| rs47229557 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Lnx1 | Mm_Celera | 5:74693831 | AACAACAGAACAAAA[A/T]AGCTACCTAGAAATC | 16924 |
| rs47249516 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74634011 | AATGGGAGTAGGACA[C/T]AAGGCTCAGTCCTCA | 16924 |
| rs47255334 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74699156 | GGCACAGAAATATCA[A/G]GAATAGTTTCATGCT | 16924 |
| rs47256762 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74687043 | CTTGTTTGCCGAAAC[A/G/T]CGGCTTTATCTCAGG | 16924 |
| rs47263095 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74606468 | ACAATGGCCTAGTGA[C/T]GTTCATCTGTTGCCT | 16924 |
| rs47263219 | snp | A/C | 0.152778 | 0.230321 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74597734 | TTTTACATGTAGAAA[A/C]CAAAAATACTTGAAT | 16924 |
| rs47265263 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74610937 | GAGGCATTGGAGACT[A/G]AGCTCAGGGCCTTTG | 16924 |
| rs47275862 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74598160 | TGGCTAAGGACAAAA[C/T]AATGCATGAGCCAGA | 16924 |
| rs47277785 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651424 | GCACAGCGGGACAAG[A/G]TATCGACCATGAAAG | 16924 |
| rs47281608 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74616046 | TATTAACAATTCATT[A/G]GAAGGTGACAGAAAA | 16924 |
| rs47282944 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74616616 | TTTCCTTAGTAGTCT[A/G]TAACTCCACATACAG | 16924 |
| rs47298556 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74629333 | TATGTTAGTCTTCTC[C/T]GTTTATCACACAAAC | 16924 |
| rs47303582 | snp | A/G | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650466 | CAATAAGTTATCCCT[A/G]TAGACGGGAATGGGA | 16924 |
| rs47320601 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74696126 | ACTTTGGCTGTTGGT[C/T]CTTGTTCTGTCTTTC | 16924 |
| rs47331473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681649 | CATACACTGGGTCCC[C/T]GGCTCCCAGTACTCC | 16924 |
| rs47332288 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74662568 | ATAAACAAATTAAGT[C/T]AAGCAGCTTGAAAGA | 16924 |
| rs47343901 | snp | G/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74702536 | AAGAATCAGATCAAC[G/T]TCACCAACAAGTAGA | 16924 |
| rs47347212 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74665770 | AGACCTCTATCCTGC[C/T]GCCAGTGACCAGATA | 16924 |
| rs47361640 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596673 | AAGGATCAACGGTAG[C/T]GTAGGACGTGGGGGA | 16924 |
| rs47363212 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74664789 | ATAATACTTATTATT[A/C]AATGGTCCCCTTCCT | 16924 |
| rs47374067 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694616 | AAGAACAGAAAAATA[G/T]AAAGGGTCTCTGCAG | 16924 |
| rs47380426 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74695291 | GACCTCTATTTGTCT[G/T]GAACTCTGGGGACTC | 16924 |
| rs47390016 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74672194 | AGTGAAAAAGAAACA[A/T]TTTTTTTTGAGATTC | 16924 |
| rs47393962 | snp | A/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646011 | TATGTCCACCGACCT[A/G]ACATTCTTGCTCAAG | 16924 |
| rs47396658 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74673887 | AAGGAGGAAAATGGC[A/G]GCTCCATCCCAAAAG | 16924 |
| rs47404084 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697750 | CTCAGAAGAGGCCAC[A/G]TGACTGACAGAGTGT | 16924 |
| rs47415554 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74600218 | CACCCACTGGGAAAC[C/G]TGGCAGCTGGTTCAG | 16924 |
| rs47425942 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651355 | GGAAAATTCTTCTTC[A/C]ATGCCCGTCTCTGTT | 16924 |
| rs47433573 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74691523 | TTTGGGGATGCTTTC[C/T]GCTATCTTATTCATC | 16924 |
| rs47434403 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74690136 | TCATAGAAAGCAAAT[A/G]GATAAATACATCATT | 16924 |
| rs47434490 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74693856 | GAAATCCCCGAGGTG[C/T]AGAGTTTTTGTTAAT | 16924 |
| rs47444631 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683795 | TCCGCCGTCATAACC[A/T]GCATGGGAAACGCAT | 16924 |
| rs47448075 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74637819 | TTTAGACTGGCCTTT[A/G]TCTTCCTCACAGACT | 16924 |
| rs47456550 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74659345 | ATTGGTATTACTAGT[C/T]CCTTTTATCTCAAGC | 16924 |
| rs47457414 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602913 | ACTTTAGGTAACTGG[A/C]AAGACTGTATAATAG | 16924 |
| rs47483720 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638016 | GTTTCAAAATCATTA[C/T]GCCTATACTCAAGCC | 16924 |
| rs47491360 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694544 | AAAGAGGGAGCAGGA[A/G]ACTCATTAATGAAAC | 16924 |
| rs47496407 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74674076 | ACTCTTAATAGTGAG[G/T]ATCTTGCCTGTGTTC | 16924 |
| rs47500049 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596986 | ACTCTACCACATTTG[G/T]AACTGACTTGAATTA | 16924 |
| rs47515075 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | GRCm38.p3 | 5:74600463 | GAGCTGCTTAAGAAA[C/G/T]GAAGTTTTGGAGCTA | 16924 |
| rs47516264 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593388 | TGTATCAGAAGGGAT[A/G]GGGCGCGGCTGCTGT | 16924 |
| rs47521645 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74667821 | TACCCACATGTTCTA[C/T]CCGGAGGACATTAAT | 16924 |
| rs47535335 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74670715 | CGTGCAATGCTTTGG[A/G]TCATTCCTTAGGATT | 16924 |
| rs47537618 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74686559 | ATATCCCGTGGCAAT[A/G]TGTCTTTTCCTTTGA | 16924 |
| rs47542297 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593507 | GCCTTCCGTATTTTA[G/T]GCAAGCTTAGTTGGA | 16924 |
| rs47554783 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74601128 | AGAAAAACAATGGCC[A/G]AGTTTGGAAAACAAT | 16924 |
| rs47556532 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74696296 | TCCCCTGGGACACTT[C/T]TTAATTTGCTAAGGT | 16924 |
| rs47593382 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74637235 | CAAGGGGAAGATACT[C/T]GGAGCACATGTGTGT | 16924 |
| rs47598861 | snp | A/G | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652939 | AGGCCCATTAGTTAT[A/G]GACCCTCAAGGATGA | 16924 |
| rs47600703 | snp | A/G | 0.142012 | 0.225474 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656586 | GAAGCAGGAACCTGA[A/G]CAAGTGACGACATTT | 16924 |
| rs47601267 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698934 | TATGACCGTGATCTC[A/G]GCCCCCTGTAGTCTC | 16924 |
| rs47606964 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74690182 | GTTAGTATTCTTCTA[C/T]TGAAAGAACCAATTT | 16924 |
| rs47610096 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | GRCm38.p3 | 5:74616642 | TACAGCGTCATCATC[A/G]CAGCAGCGCATTACA | 16924 |
| rs47612834 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604771 | AAGGAGAGCTACTTC[C/T]ACTCCCTCTGCTCTG | 16924 |
| rs47614727 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74669614 | TATAGTGTCCAGGTG[A/G]AGAACCGACTCGCCC | 16924 |
| rs47617422 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596862 | AGTGTGTGAAAGATG[A/G]GGCAGTTAGAGCCAC | 16924 |
| rs47619808 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74661979 | GGACTCCCTAGTGGG[A/G]AGCTAGAGGCACTAA | 16924 |
| rs47623991 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74684552 | TGCTGGACAATGTGA[C/T]TGGCATGTGTAAGTC | 16924 |
| rs47626881 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701105 | TGTCATGGCAACTTC[C/T]CAGGGAGAACACCTG | 16924 |
| rs47627867 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593888 | ACCACTGACTGCTTA[C/T]TCTCACACCACGCAC | 16924 |
| rs47636278 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74633014 | GCATGGAAAGGAAGT[C/T]CATGACTTGTCAGTG | 16924 |
| rs47638315 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698050 | AGAGGAAACTTGCAG[C/T]ACATGTTTGAAGTGC | 16924 |
| rs47649486 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74629206 | ACTGGTGATGATTTA[A/G]CTAACACACTGTTCT | 16924 |
| rs47651145 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74671720 | AACATGGAACAAGGT[C/T]GCCATGCTCTGTGGA | 16924 |
| rs47656547 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74647088 | GAGGCGAGACTTTTG[A/G]GATTCCTAGGAAGGG | 16924 |
| rs47656954 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74644810 | TGTCACCAGAAACTA[C/T]AGTGAAATCAATGGG | 16924 |
| rs47658370 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74616850 | TCCCAAGATTATTTC[C/T]CTTCCACAGTAAAGG | 16924 |
| rs47679130 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74694192 | TTCCTTGACCTTATT[C/T]ATGCCTTAAGTCTCA | 16924 |
| rs47700486 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Lnx1 | Mm_Celera | 5:74685431 | GAGATCACAGCGCTG[C/T]AGCACCTCAGTGCAG | 16924 |
| rs47703908 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74671855 | ACAAATGGGAAAGCA[C/T]GTGTTGAAGGCTGGG | 16924 |
| rs47717938 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74614211 | AAGGTAAGAGTGCTT[C/T]TTTGTTTCATGCCCA | 16924 |
| rs47725499 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74639847 | CTTTCTGGTCCTGAA[C/T]ACAAGCCCCCTTCCA | 16924 |
| rs47734161 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74660888 | CATCAAAGGAGACAC[A/G]GTGATTTACAGCAAA | 16924 |
| rs47748771 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74671777 | TTCAATGAGCCTAAT[A/G]TAAATGGACCAGAAA | 16924 |
| rs47749953 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74688707 | TCTTCCTAACCCTGC[C/T]ACCCTCTGTCTCCCA | 16924 |
| rs47753575 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74612886 | ACTTGGTTTAGCACC[A/G]AGCAGCCCAAACATT | 16924 |
| rs47771757 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Lnx1 | Mm_Celera | 5:74696938 | AAAGCTGCTCTACTC[A/T]CGGACACAGCCATGG | 16924 |
| rs47779625 | snp | A/C | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74657441 | CTCACTTCCCAGGCC[A/C]TCCCTGGCTCTCTCT | 16924 |
| rs47784056 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602697 | GGAGCACACGACTAC[C/T]AATATGCTTTTATCT | 16924 |
| rs47796263 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74609258 | TGCTTCCCATACATG[A/G]ACATGAAACTTAAGG | 16924 |
| rs47797055 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74663123 | ACGCCTAGGGGAGTG[C/T]CTTGAAGATTTCAAT | 16924 |
| rs47810355 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74684173 | GGGGAAGCAGGGGAT[G/T]CCAGTCACCAGCAGC | 16924 |
| rs47814496 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653344 | GAAATAGCATAAAAC[A/G]AGGTCAGAATGCTTA | 16924 |
| rs47817255 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74694574 | CCTGCGAATGACATT[C/T]ACCTGCAAAGTGTTC | 16924 |
| rs47821818 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593435 | CTCCCCAGCACGTGA[C/T]GGCCTACAGCATTCA | 16924 |
| rs47825007 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74672361 | TTCCTCCTATACCCA[C/T]GGTAGAATACAACTG | 16924 |
| rs47857091 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674402 | CTTCAAGAAGGACCT[A/C]GCTGCCAGTCAGAAA | 16924 |
| rs47861133 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74684198 | AGCAGCAGGTAGCAC[A/C]TCTCCTTTCTGTCAC | 16924 |
| rs47868765 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74683055 | CAGCTCTTTCCCAAG[C/T]GCTCTTCATTACCAA | 16924 |
| rs47881342 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74663031 | ATTAGGGAAGTAAAA[A/T]TTTTAAAAGTTAGAA | 16924 |
| rs47887189 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Lnx1 | Mm_Celera | 5:74662871 | TGAAAAACTGCCTTA[C/T]ACTCAGGGGAATGTC | 16924 |
| rs47907994 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74616619 | CCTTAGTAGTCTATA[A/G]CTCCACATACAGCGT | 16924 |
| rs47910146 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74636237 | TCGATAAGGATGAGG[A/G]TAGTTGAAGGGAAAA | 16924 |
| rs47937511 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74609473 | TTGGTTGTTTTTAAA[A/C]ATTGATTTCTTTCTC | 16924 |
| rs47939871 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74630200 | GCTGTGAGCTCTGAA[A/G]TAATTAGATCAGATG | 16924 |
| rs47948394 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Lnx1 | Mm_Celera | 5:74642106 | TCCGAGTGCATGCTC[C/G]CTTGGATGCTATTCT | 16924 |
| rs47970032 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646640 | AACTATGTACCAAGA[A/G]GAAGAACGCCTCTTT | 16924 |
| rs47974557 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Lnx1 | Mm_Celera | 5:74610749 | GCCAGCTTCTTGAAA[A/G]ATGTCTGGGCTGGAC | 16924 |
| rs47993239 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74665498 | CTTCAGAATCCTTTC[A/G]TGACGTCTCAAGGAA | 16924 |
| rs47993720 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74689593 | CTCCCACATTAGCAA[A/C/T]GGCAACAATCTCTTC | 16924 |
| rs48010237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593899 | CTTACTCTCACACCA[C/T]GCACTTTATAAACAT | 16924 |
| rs48012908 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Lnx1 | Mm_Celera | 5:74686586 | TTGATACAGGAGTTC[A/C]CAAAGGATGGGATTT | 16924 |
| rs48022892 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74673976 | TAGGTGGTCCTGAGA[A/G]CCCACCCGTTCTCAG | 16924 |
| rs48037098 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74633131 | AAAGCTATGCCTTTC[C/T]TTGGAGACATAGCCT | 16924 |
| rs48046678 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74693967 | ATAGCCAGGTCACTC[A/G]TTCCTAGGCAGAAGC | 16924 |
| rs48051065 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74693628 | ACGTGTGAACCCACA[C/T]ATACACAGATACCTA | 16924 |
| rs48064606 | snp | G/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74662551 | GAAGCTCACTTCCAG[G/T]CATAAACAAATTAAG | 16924 |
| rs48064800 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703151 | CCCCGTGTACAGATC[C/T]GAATGCGAATGCCTG | 16924 |
| rs48064954 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74615810 | TCTTCACCATCGGTG[C/T]TTGCAATGCGAGCAC | 16924 |
| rs48068680 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74601924 | GAGATAGGAGAAATG[A/G]CAAGAAATTATAGAC | 16924 |
| rs48074158 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74690331 | AGTTCTGACCTAACA[C/T]TCATAAGGCCCAGCA | 16924 |
| rs48084053 | snp | A/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74684289 | GTTTATGTCACCTTG[A/T]TACAGCTACAGCTAT | 16924 |
| rs48085765 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651415 | GTCTCCGAAGCACAG[C/T]GGGACAAGGTATCGA | 16924 |
| rs48086204 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74665503 | GAATCCTTTCGTGAC[A/G]TCTCAAGGAATTCTG | 16924 |
| rs48100565 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648469 | GTGAGTGTTGCCAAC[C/T]TAGAACATGTGCACA | 16924 |
| rs48110955 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74608128 | TGGTAGAAATCTGGA[C/T]CTTATAAATTTGGAC | 16924 |
| rs48122441 | snp | C/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703403 | CTAGTGTTTTTCTGT[C/T]CCAATATTATAACAA | 16924 |
| rs48126819 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Lnx1 | Mm_Celera | 5:74684118 | CACAGAGGAATGCCC[A/G]GGCACACAACACCGA | 16924 |
| rs48134590 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74612501 | ATGGTGAGGACTGAG[A/T]CTCCAGGCTGCCCTC | 16924 |
| rs48141186 | snp | C/T | | | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74702753 | CAGATCCCTTTTGGG[C/T]CAGAGGTCTAAAGAG | 16924 |
| rs48159251 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74696213 | GACAGCATTGCTGGT[C/T]TTGTCTTCTCTCTTC | 16924 |
| rs48208634 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74678526 | GTGTTCATGTATCTC[A/G]CTAACTCCAGGGGCT | 16924 |
| rs48221498 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74608152 | TTTGGACTGGATCTC[A/G]AATCTCTCAAGGAAG | 16924 |
| rs48227811 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638452 | GTGAATAGTAGACAT[A/G]AATGAAAAGAACAAT | 16924 |
| rs48236469 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650217 | CGTTCAGAGAATTTG[C/T]TAATTCCCAGGTTGT | 16924 |
| rs48240516 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74664192 | GGGGTAGGGGGGCGC[A/G]GGGAATTGAAAGCAG | 16924 |
| rs48245645 | snp | A/G | 0.5 | 0 | intron-variant | Lnx1 | Mm_Celera | 5:74696873 | TCTGTGAAAAGACAG[A/G]GATGGCTGTTTATGT | 16924 |
| rs48256081 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74644881 | AGATTTGGCAGGGGG[A/G]GGGGGGCATCAGGGA | 16924 |
| rs48260957 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674364 | CTGTAAGCTAAGGAA[A/G]GCAATAAGTGACAGC | 16924 |
| rs48281822 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701529 | TGGGCACAAAGGTCA[A/G]CTAGAAAAGAGACTA | 16924 |
| rs48287453 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602128 | TCATGATTGAAATCA[C/T]AGACTCAGGCAGGAA | 16924 |
| rs48291943 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Lnx1 | Mm_Celera | 5:74613767 | ACGTGGACGCTGGAG[A/G]ATCCCACATGGCTCA | 16924 |
| rs48292948 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74594050 | GTGCACACTGCCGCT[C/T]TGCACTGCCTGTCAA | 16924 |
| rs48294027 | snp | A/T | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646430 | TAAGAAACAGCTCTG[A/T]ATGACTTCGAACCCA | 16924 |
| rs48300682 | snp | A/G | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654063 | TTTTTCTTGACGTCC[A/G]GCCACAATGAGTGCT | 16924 |
| rs48306386 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74672566 | GGACCACCTAGTGAG[C/T]GACAGACAAAACCAA | 16924 |
| rs48308517 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683906 | CAGATTCATGACCTA[A/C]GGTATGTGACCTTTA | 16924 |
| rs48311762 | snp | G/T | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | GRCm38.p3 | 5:74598556 | AACTAGGAGAGTCGC[G/T]GCTGTCAGACCTAAG | 16924 |
| rs48313587 | snp | C/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703853 | CATCAGCCTGTTGAA[C/T]TGCTGTGTGTCTGTG | 16924 |
| rs48320509 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74616798 | AGCACTCCCCTGCCT[C/T]AGCACCATTTCTCTT | 16924 |
| rs48336588 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74690784 | ACAGGGCCTGCAAAG[A/G]GCAAGCTCCAGAAAA | 16924 |
| rs48340870 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697469 | CCACTAAGACTCCTG[C/T]ATACTTAGAATAGCA | 16924 |
| rs48351324 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74630653 | CCATTCCGAGACACT[C/T]ACTCCTCTCACATCC | 16924 |
| rs48353405 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74595707 | CCCAAATGTAATCTA[C/T]GTGTAAAATCTCATG | 16924 |
| rs48358404 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74668067 | GCTGCAGAAAGTGTC[G/T]TCTGCCCTTGCTTCA | 16924 |
| rs48364120 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74687911 | CTTTGAACATATTCC[A/G]GTGCACACCCCTGGT | 16924 |
| rs48364902 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74676065 | GGAAGCTCTGCCACT[C/T]TACAGTGTCAAGAAA | 16924 |
| rs48373647 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650925 | ACAAAGGAAAAGACT[C/T]TGCACCTGTTCTCTT | 16924 |
| rs48380487 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611767 | AGACCCTGGGTCTGC[A/G]GGTGTCATAGAAACA | 16924 |
| rs48382391 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Lnx1 | Mm_Celera | 5:74606045 | GACTCACTGTGGTAA[C/T]TCCAGCCACATGACC | 16924 |
| rs48399481 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Lnx1 | Mm_Celera | 5:74693853 | CTAGAAATCCCCGAG[A/G]TGCAGAGTTTTTGTT | 16924 |
| rs48401952 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74700451 | CCAAATGCTCATGGA[A/G]TCTGAGGTAGAAGAT | 16924 |
| rs48402240 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | GRCm38.p3 | 5:74640840 | TGTGCACAGTAGGGC[A/T]GTAAGATGCCATGCA | 16924 |
| rs48405977 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74694026 | TGTCAGTAACTGCTT[C/T]CCACAGTGGCCCTGG | 16924 |
| rs48406041 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74599876 | GACCAGCATTCAGGA[A/T]GGGACACGTCTTCCT | 16924 |
| rs48408983 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650118 | TAAGCTCTGTGTCCT[C/T]GGCACTAACTTTCTC | 16924 |
| rs48425583 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Lnx1 | GRCm38.p3 | 5:74640475 | CTGAGATACGGTTGG[C/G]TAGTCTCTGAACGGG | 16924 |
| rs48429103 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74608054 | CCAAGGCTTGACTCC[A/G]AGAAGTTTACATTGC | 16924 |
| rs48434074 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646717 | ACTGGATCTGAAGAC[C/T]GGCTCACAAGGAAGG | 16924 |
| rs48434635 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74664559 | AGGAATCTAGCTGTC[C/T]GGAAGGCACAACTGT | 16924 |
| rs48437439 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593121 | CTTGTCCTAGGAAAA[C/T]TGTACTAGGAAATAC | 16924 |
| rs48441165 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74594904 | AAAACAGATCTCACA[G/T]GATGCCATTATTTTA | 16924 |
| rs48453245 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74603221 | AAGCTGTACCACCGA[C/G]ATGAGGCCAGGACAG | 16924 |
| rs48454173 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | GRCm38.p3 | 5:74595584 | TTACCCTATAAGATG[A/G]TATTTTCCATTCCAG | 16924 |
| rs48467944 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74693913 | GTTGGGCAACATGGT[A/G]ACAACATTTCAAACT | 16924 |
| rs48503620 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74635948 | CCTCCCTCTGGTTTG[C/T]AGTCTCTCTCCCTCT | 16924 |
| rs48506085 | snp | A/C | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679182 | CTAGACCAAGAAGGA[A/C]GATATGCTGCCATCT | 16924 |
| rs48512148 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74630112 | GGGCCTGCAGTTGAT[A/G]GGTTTTAGGCACGCA | 16924 |
| rs48516532 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74603424 | AGGGCAAAGAGCAAC[A/G]GGAAATTCAGCAGAA | 16924 |
| rs48530384 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74665234 | ATGTGACACTGAGCA[A/G]CTGAATAAAGACTGG | 16924 |
| rs48537052 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74606391 | CAGCTCATAGAGACA[C/G]GAGACTGGGTCCCCT | 16924 |
| rs48538046 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74615991 | AAAGGCTACTGTCTC[G/T]GTGTTCTACAGGGCC | 16924 |
| rs48539976 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674865 | GCCAGCCAATCCCCA[A/T]GGTTCTGTCTCTGAG | 16924 |
| rs48554595 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74617085 | AGCATAAGCAGATTT[A/G]AGTTTAGTCTATGCA | 16924 |
| rs48558358 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74681636 | ACCTATCAAACTCCA[C/T]ACACTGGGTCCCCGG | 16924 |
| rs48560267 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74655897 | TGAGAATTCTGTACA[C/T]GTCTTGGTATCCAGT | 16924 |
| rs48560425 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74680652 | CAGGAATAGAAACCC[C/T]GACTAAGACAGTGGT | 16924 |
| rs48574804 | snp | G/T | 0.32 | 0.24 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651833 | ACAAGTCTGACTGGC[G/T]TCTTTCATCCATGCA | 16924 |
| rs48577974 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74631537 | TCTCACAGGAATTGA[A/G]GAAAGGGAAAGAATA | 16924 |
| rs48579279 | snp | A/C | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74657702 | CTGAAGTTTTCCTCC[A/C]TGACTTTAATAAGTA | 16924 |
| rs48583687 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74693936 | TTCAAACTGGCCCTG[A/G]GGCCCCACATCAGAC | 16924 |
| rs48584544 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683655 | ACAATGCCTCAGACC[A/T]GGGCAAAATTATCAG | 16924 |
| rs48589992 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697254 | AAACTTCTACACACT[C/T]TAGAATTGAAAAAAA | 16924 |
| rs48590948 | snp | A/C | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74672977 | GTTCTGGCGGCTCAG[A/C]CCACTCTCATGTAGA | 16924 |
| rs48594434 | snp | A/C | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646071 | GTCTGAAATGGGGAG[A/C]GATGATTGTTCCTCT | 16924 |
| rs48596858 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Lnx1 | Mm_Celera | 5:74634121 | AAGGGCTCCTTGCTG[A/T]CTGTGACCTGACCCA | 16924 |
| rs48616755 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74684290 | TTTATGTCACCTTGA[C/T]ACAGCTACAGCTATC | 16924 |
| rs48617402 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74600891 | ATTGAATCATAACCT[A/G]TGGTGTGGAAGCAGC | 16924 |
| rs48618444 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74652072 | AGAAGAATAGCTATA[A/G]ATATCTGTGTAAACG | 16924 |
| rs48629225 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74610859 | ACAGGGCCTTACCAA[A/G]ATAGCACTTTCGTTT | 16924 |
| rs48634904 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74596254 | TAGAGCTAAGGTTGA[A/C]CATGTGATCACGGGA | 16924 |
| rs48636112 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74615288 | CATCTAACTCTTTAA[A/C]AATCCCCAGAAAGAA | 16924 |
| rs48637958 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74645145 | CATGACAATATCAAG[C/G]CAGATGACTAACTAT | 16924 |
| rs48644651 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | GRCm38.p3 | 5:74680867 | AAATGCCAGAAAAGG[A/G]CCCCTGATAGAGTCA | 16924 |
| rs48649091 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74639340 | CAAGAGAGCAAACTC[A/G]TGCTTACCCTGATCA | 16924 |
| rs48663328 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74644006 | CATCAGTAAGCAGTC[A/G]GCTCTCAGCCTTCGT | 16924 |
| rs48663748 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593976 | GAGAAGCCTTGAGGT[C/T]TAAAGGAGTGAAGTT | 16924 |
| rs48676336 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74675290 | CTCTGTCCACTCAGA[G/T]GATTTGAGAGACTTT | 16924 |
| rs48688576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681508 | CTCCTGGCATTATAC[A/G]TTGGTTAGAAGGCTG | 16924 |
| rs48692416 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653182 | TTTAAAATGCCACAG[C/T]CAAAAGGCAGGACAA | 16924 |
| rs48693784 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Lnx1 | GRCm38.p3 | 5:74661465 | TTGCAATCTGCTAGG[A/G]TACCCAGCACAGCAA | 16924 |
| rs48702402 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74640856 | GTAAGATGCCATGCA[C/T]GTGGGTGGCTGATAA | 16924 |
| rs48712075 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74669951 | CACCTAACTCCCAAT[A/G]TGCCACCCTGGATGT | 16924 |
| rs48717999 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74651136 | CTGGATTTATAGTGT[A/G]TGAGCCAGTCTGTTT | 16924 |
| rs48731409 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74613209 | AAAGTGATAAATCTC[A/G]CAATGGACGGCTAGC | 16924 |
| rs48732808 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74673441 | AGTAGGTCACTGAGC[A/G]GGTGATGCCTACTTC | 16924 |
| rs48735461 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74613309 | TTCATGCACAGCCCT[A/G]ACTTACGAGTCAGTG | 16924 |
| rs48737859 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650959 | AAATTCTTTTAGCAT[G/T]TGAACCTGTGGATTC | 16924 |
| rs48744085 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604992 | ACAAAGGAACACTGA[A/G]AGTCTAACAGGGAGC | 16924 |
| rs48752299 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74635663 | TCTGAGGCTTTTGAT[A/G]CTCCATTATCTCCAC | 16924 |
| rs48752323 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646179 | GGATGTCAAGAACTG[C/T]TGATGGAGAGGTAGG | 16924 |
| rs48757883 | snp | C/T | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654833 | AAAGATCAGACAGCC[C/T]ACTCATCCCTGGGCC | 16924 |
| rs48759244 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74615389 | CTCATTTCTTCAACA[C/T]TTAAATATCATTCTT | 16924 |
| rs48761722 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74632959 | CTGTAATTGGAGAGC[A/G]GAGCACTTGCCCGTG | 16924 |
| rs48762071 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | GRCm38.p3 | 5:74666279 | GAAAAGACATGGAAA[C/T]TTTTGAGGGAGCATA | 16924 |
| rs48764757 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74649349 | TTGTACTGCCTTTCC[A/G]GCTTCAAAGACCATG | 16924 |
| rs48767890 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74684367 | AGAAGGCAAGTCTGT[A/G]GGACATTTTCCTGAT | 16924 |
| rs48770875 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74696041 | TTTCAACATATCTAG[A/G]GGTGACATGCAGTTG | 16924 |
| rs48802903 | snp | C/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698255 | TCTGCTCCTATCTGT[C/T]TTAAAATATAAAAAG | 16924 |
| rs48804427 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74702556 | CAACAAGTAGAGGCC[A/G]GATTAATAATCAGGA | 16924 |
| rs48805367 | snp | C/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74686261 | CCTTTAACCAGTAAG[C/G]AGCAGAGTAACCACA | 16924 |
| rs48814663 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74658069 | TTTCATCGTTCTCCC[C/T]GACCTTTACCCTGGA | 16924 |
| rs48834439 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74679412 | CTCCTTGCATTTCAG[A/G]ATGAACAGTTGGATG | 16924 |
| rs48836494 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74686717 | AAACACTTATGTAAA[A/G]GATACAATTTTAGGG | 16924 |
| rs48837381 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74614134 | GGCACGAGAGTCTCT[C/T]TTTCCACCCGTGTGA | 16924 |
| rs48841508 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674775 | ACTCAAGGGAGACTC[C/T]GCATGTGGAAGCTGA | 16924 |
| rs48858449 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74636428 | TACATCCCCACCCTA[A/G]CATCCACCCATCCTG | 16924 |
| rs48862858 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656701 | TAGGAAGAGACACAG[A/G]GTAAACTTTTCTTTA | 16924 |
| rs48869889 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611988 | CAGAGACAGACACTG[A/T]TATATGCACACGCTG | 16924 |
| rs48878486 | snp | A/G | 0.124444 | 0.216185 | missense | Lnx1 | Mm_Celera | 5:74685754 | GAGGCTCGGGACTGG[A/G]ATCTGGGTCATCTGC | 16924 |
| rs48886986 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74633986 | TTCCAAGTCTTTGGT[A/G]TGAGTTGCTAATGGG | 16924 |
| rs48894477 | snp | A/G | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656278 | AACAGGACACATGAC[A/G]GGGTTTAGCAGAAAC | 16924 |
| rs48900647 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74672404 | TGTACCCGAATGGAT[C/T]GCTATTCACATGAAG | 16924 |
| rs48902356 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74640642 | CAACAGTTGGGGCAA[C/T]TCACACTGACAGTTA | 16924 |
| rs48919053 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Lnx1 | GRCm38.p3 | 5:74636119 | GGCCGGTGGAAGCAA[A/G]CAGCCACCAGCCTCT | 16924 |
| rs48922232 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74690584 | GGGAGAGTTTGTCTC[C/T]CTGAGGCTCCTCCCC | 16924 |
| rs48945708 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74661537 | TTAAGTTTCACTGTG[A/C]CTGCTTGAGACACTC | 16924 |
| rs48946854 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74605604 | AGACACGTAACTCTC[C/T]GAAGCCATGATGTTT | 16924 |
| rs48950082 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683590 | CCCTGGTCTTGGCAT[A/G]ACTGGACAGGACCTA | 16924 |
| rs48953107 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74603608 | AGCCCTTTCTCTTAT[C/T]AGTCTTCAGGAGACA | 16924 |
| rs48957078 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74613452 | TAGATCTAGGGCCTC[A/C]CCAACAGTTCAGTTT | 16924 |
| rs48961230 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74612031 | ATGGTTCCAGGGCCA[C/T]AGAGAAATCGGGTCA | 16924 |
| rs48965615 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74670882 | AGAAAGAGTGAAAGA[C/T]AAATTAGGTAACAAG | 16924 |
| rs48967415 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74662989 | ACTGATGCATGCTGT[A/G]GTGGGTTTAAAAATT | 16924 |
| rs48971569 | snp | A/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701751 | ACCCAGGAAAGGGAC[A/T]AATCAAAGTCTATAA | 16924 |
| rs48990079 | snp | C/G/T | 0.42 | 0.183303 | intron-variant | Lnx1 | Mm_Celera | 5:74665414 | AGGCTCCAAAGCAGA[C/G/T]GGTGAGTATCTAGGG | 16924 |
| rs48996294 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74675498 | TATTTAGATAAAATG[C/T]GTTAGGACTGAAATT | 16924 |
| rs49001174 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74695031 | CACTCTATTACTGCC[A/G]AGCATCAACATGGAC | 16924 |
| rs49005354 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74643485 | CTTCCTCCCCGTTTG[C/T]CAATGTGCCCCACGA | 16924 |
| rs49014501 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74619168 | TTTTCGAGATCTGAG[A/G]AGCAAGCAACCACCA | 16924 |
| rs49018021 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74661814 | TTATTGCAGTATAAA[C/T]AAAGCTGTCTATGGG | 16924 |
| rs49019992 | snp | C/T | 0.408163 | 0.193609 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654016 | TGTACTCTTGAGCCA[C/T]GCTGCGGGTAAGCCA | 16924 |
| rs49025727 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74692716 | CATGGCTCCACCTCA[C/T]TTTTTGCGTGGTAGA | 16924 |
| rs49039890 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74633846 | ATGAAGTCGGGTCCC[C/G]AGCTCCTTCACTGAA | 16924 |
| rs49039963 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74659188 | CCTATGATTTGAGAT[A/G]GCAAACAGCACCCTT | 16924 |
| rs49041631 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656102 | TCACCCTCACTGCCA[C/T]TTATGTCTCCAGAGC | 16924 |
| rs49050414 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74638055 | ACTTTTGATCACATG[C/T]CTTCTTTTGATGCAT | 16924 |
| rs49073135 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74672119 | ACATAGAAGCAAGAA[A/C]ACATATAACATATAA | 16924 |
| rs49075086 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74696064 | TGCAGTTGCTATTCT[C/G]AATCTGTCCAGTGAC | 16924 |
| rs49080104 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74637845 | AGACTCCCTACGAAA[C/T]GCTGGAAGTTTTATT | 16924 |
| rs49082520 | snp | C/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74598589 | CAAACAGCTGCATTA[C/G]AGTAGACAGTGTGTC | 16924 |
| rs49085347 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74691947 | ACACACTTATCCCAC[A/G]CTGTGCTGAGTCACG | 16924 |
| rs49098052 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74614299 | AGGAGGGCAATGATA[A/T]TACAGGCAGAGCAAA | 16924 |
| rs49119836 | snp | C/T | | | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593833 | GCCACCTGCAGCAAG[C/T]ACCGTTCCCCACTGA | 16924 |
| rs49128322 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74633389 | AATGCAGAAATATTC[A/C]GACTTATAGGCTTTA | 16924 |
| rs49129494 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602288 | ATAAACATTAGTGGT[C/T]TCATAGCTGCCCTGA | 16924 |
| rs49136380 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74685094 | CACCATTTTTTTTTC[C/T]GAACTATAAACACAT | 16924 |
| rs49149907 | snp | A/G | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653196 | GCCAAAAGGCAGGAC[A/G]AGGGGGTCCAATAAA | 16924 |
| rs49158773 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74629011 | ATCCATTTTATTCAC[C/T]GCATTTTCCCAAAAC | 16924 |
| rs49158852 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74695331 | CAATGCTATCTTCAT[A/G]GTGTTCAAGCTTAAT | 16924 |
| rs49158970 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Lnx1 | Mm_Celera | 5:74642880 | TGGGTCCGGGGCAGA[A/G]ACCACAGAGCATGTA | 16924 |
| rs49163747 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74671415 | AGTTTAAAATGAAGG[C/T]GAAAAAAAAAAAAAT | 16924 |
| rs49197254 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74642180 | CAATATGTTCTTTTA[A/C]AGCAACCTTTGCAGC | 16924 |
| rs49198399 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74662822 | ACTAATATGCTTACC[A/G]AACAATGGTGTAGTA | 16924 |
| rs49219083 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74686457 | CAGTTCCCACAGGAG[A/G]ATCTTTCTGCTTTGT | 16924 |
| rs49219282 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646786 | TGACGCTTCCAGAAC[A/G]CTTTGTGTACTGGGA | 16924 |
| rs49220429 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74672079 | CCACTTGGGTCCTAT[C/G]AAAGCTTCACCTCAG | 16924 |
| rs49224528 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74686180 | CTTCATTACCTTTCT[C/T]GTCTGTCTGGTTATC | 16924 |
| rs49235451 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Lnx1 | Mm_Celera | 5:74616956 | TTGGATGTAATATAC[A/C]GCGCCGCCTAAGTCA | 16924 |
| rs49251871 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74679643 | GTCTTGAAAGGAAAC[A/G]GTCTCGGCTCCCTTC | 16924 |
| rs49263249 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74674388 | TGACAGCGATTGTGC[A/T]TCAAGAAGGACCTAG | 16924 |
| rs49264529 | snp | G/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74613164 | TACAGTGTACTTACA[G/T]TAAAGAAATAAATCT | 16924 |
| rs49273890 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674012 | TGTGTATATACATGT[C/T]CCTACATGCCCCCTA | 16924 |
| rs49281748 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74610535 | TCTAAGTATGAAGAC[A/G]GGACTTTGGCCTTTT | 16924 |
| rs49308135 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652840 | CATTTGAAAAAAAAA[A/T]GTTCATTATTTTAAA | 16924 |
| rs49308296 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74651052 | AAAATCAGCCAGCCT[G/T]CAGGAAAGCAGGACC | 16924 |
| rs49334042 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74691347 | ACCTAGGGTTATAAG[G/T]AGAAGCATGGAGCTT | 16924 |
| rs49338639 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74683692 | TCACTAACACGCACC[A/C]GCACCACCATCTCTT | 16924 |
| rs49338845 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74684210 | CACCTCTCCTTTCTG[C/T]CACCAATGTGTGCAC | 16924 |
| rs49341185 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74604497 | TTCTTGGGTTTAATT[C/T]TCAAGAAGCCTTGGA | 16924 |
| rs49342454 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Lnx1 | Mm_Celera | 5:74642255 | TAAACTCCCTGTTTA[A/G]TTTAGACAAAGCCTA | 16924 |
| rs49357528 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Lnx1 | GRCm38.p3 | 5:74682068 | AAGCACAAGGCTGTG[A/C]ATCATAAATATATTA | 16924 |
| rs49361653 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74664588 | GTGTGTCCATTCATC[C/T]TGACATTAGATGTTG | 16924 |
| rs49369060 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Lnx1 | GRCm38.p3 | 5:74640892 | AGGTGCTTGGAACAC[A/G]AGAAGCAGGGGAGAC | 16924 |
| rs49384085 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646113 | CTCTTCAATGTTTTG[C/G]CCACAGCTGTATAAA | 16924 |
| rs49408759 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Lnx1 | Mm_Celera | 5:74695774 | ACACATGTTGGTGGC[C/T]CTATATGACTTGAAA | 16924 |
| rs49410209 | snp | C/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74704055 | TGTTCTAACACCTCA[C/T]GGCCTAGCCGTGGTT | 16924 |
| rs49410412 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74596045 | AATCTCCTTATTTTT[C/T]TGGATAATGTTTAAG | 16924 |
| rs49424714 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74612172 | TTTTAACCCCCAAGG[C/T]GATGGTATTACCAGG | 16924 |
| rs49426182 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74594814 | GAGCAAAAAGAAATA[C/T]CTGTTGATTAAAATT | 16924 |
| rs49429110 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74614043 | TAGCCCTCGAGATAC[A/G]AAGTAGGCTCACGTG | 16924 |
| rs49429988 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656233 | TGGAGGATTTGTAGA[C/T]ATGAATTTCTACTCC | 16924 |
| rs49447578 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74675337 | ATATACAGGAAGAAT[A/G]TTTTTACACTAAAAT | 16924 |
| rs49463495 | snp | C/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74693407 | TAGCAGATGGGAAAA[C/G]TGTAGGTCAAAGGAG | 16924 |
| rs49483565 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74640805 | GGTCCCTGGAGAGGA[C/T]GGTGGAATTCTGGTT | 16924 |
| rs49493008 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74671375 | TCTTTTTTCCTTTTG[C/T]TGTCCAACGTTTTCC | 16924 |
| rs49498472 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74650790 | CCATCAGAGGTCATG[A/C]AGAGCCTTCCCTCAA | 16924 |
| rs49508809 | snp | G/T | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703541 | TTGGTAAAACTTCAG[G/T]CATTCCTACCTCGGC | 16924 |
| rs49513498 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Lnx1 | GRCm38.p3 | 5:74616351 | GAATAAGCTAATAGG[G/T]TTTGGGAAGTTGATG | 16924 |
| rs49515783 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74598032 | AATGAAAAAATACTG[C/T]GTCAGCTTTTGTATT | 16924 |
| rs49545493 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | GRCm38.p3 | 5:74616116 | CCATACAGTGGAACA[C/G]AGACCCTCCTTGGCA | 16924 |
| rs49545947 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698189 | ATCTCGAAGCCTGCA[G/T]ATGTCTGGTTTGGGA | 16924 |
| rs49550102 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Lnx1 | Mm_Celera | 5:74643384 | GTAACTACGAAAAGG[A/C]CTCCTCTGTCTAACA | 16924 |
| rs49566100 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Lnx1 | Mm_Celera | 5:74695726 | CCAAGGGGAAAGAGC[C/T]TAGACAAACACTGCC | 16924 |
| rs49569636 | snp | A/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654846 | CCTACTCATCCCTGG[A/G]CCAGACAGATGCTTC | 16924 |
| rs49583330 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74684946 | AGGTATGCCCTGGTA[A/C]GCTATTTCTTCCAGC | 16924 |
| rs49591493 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74676742 | TTAGAAGTACACTGT[A/G]AAGTAGTTGAGGGTG | 16924 |
| rs49614684 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74616407 | TTGCCCATCTCTGAG[A/G]TTTTAGTACTAAGCA | 16924 |
| rs49618958 | snp | A/C/G | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74654255 | AACACTTTTTGCCTC[A/C/G]GTTTCTCTTTTGGAT | 16924 |
| rs49619778 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74637478 | TAAGACAGAGATGAC[A/G]CCTTCCTTCCTCCTT | 16924 |
| rs49626199 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700707 | GGCTGGCAGACCACG[A/C]TGCCTGGCTCAGGGA | 16924 |
| rs49632786 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697831 | TAAGCCTCCCATCAC[A/G]CATATGCCGTTGCCA | 16924 |
| rs49638210 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611712 | AGAACCTGGATTCTT[A/G]TCAGTCCTCAAGCTG | 16924 |
| rs49648239 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74644406 | TTAGCTGTTGTTAGG[A/G]GTGGGACTTGGAGCC | 16924 |
| rs49657031 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74605202 | ACTAGTGGAAACCCC[C/T]AAAGGGAATCCAGAC | 16924 |
| rs49676389 | snp | A/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Lnx1, Gm32304 | Mm_Celera | 5:74658347 | CATTAGTTGGCTCTA[A/T]TCCTCTTAATTCTGT | 16924 |
| rs49680503 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lnx1 | GRCm38.p3 | 5:74679180 | TCCTAGACCAAGAAG[A/G]AAGATATGCTGCCAT | 16924 |
| rs49686254 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74634100 | AGTGCAAACTCACCT[C/G]TAGGGAAGGGCTCCT | 16924 |
| rs49688975 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74679664 | GGCTCCCTTCCTGCC[C/T]GAAACTACTAGGAGA | 16924 |
| rs49698154 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674249 | CCTCAGGACTTGCTT[C/T]GACAGTTCATACTCT | 16924 |
| rs49707571 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651377 | GTCTCTGTTCCTTGG[A/T]CCAAAGACCTAGAAT | 16924 |
| rs49716275 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74637477 | CTAAGACAGAGATGA[C/T]GCCTTCCTTCCTCCT | 16924 |
| rs49723300 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74682530 | AAAAATGAGAAAAAA[A/C]GAGCAAAACGTCTTC | 16924 |
| rs49726363 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74668436 | TAGGAGAACCCTAGA[A/G]TCCGGTAAAGACCCT | 16924 |
| rs49728559 | snp | C/T | | | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593806 | TATGAAGACTGAGGA[C/T]CAAACTTGGGTGCCA | 16924 |
| rs49737993 | snp | A/C | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74694286 | GAACGGAGATACATT[A/C]TTCCTTGCCTTACAG | 16924 |
| rs49738429 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74687475 | GCCCTTACTTGTTCT[A/G]CTGTAAGGAAGGAGA | 16924 |
| rs49747262 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74613958 | TCTGCAAATAAGGCT[A/G]GGTCTGTGGCTCTTA | 16924 |
| rs49751192 | snp | G/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74683872 | AGAGAATGCACTCAT[G/T]TTTCAGAAGACAAAG | 16924 |
| rs49756760 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74610462 | TTGCAAGCTGGAGTT[A/T]AACACTGCCCAGCGC | 16924 |
| rs49757064 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681836 | GAACGTGATACAGCT[A/G]TACCCCAGATGCAAG | 16924 |
| rs49768167 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74662681 | CACATAGAGAAATCA[A/G]GAGACTTATGAACCT | 16924 |
| rs49776227 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Lnx1 | Mm_Celera | 5:74664266 | CAGGTACAAGACGGA[C/T]GAGATGGAAGGCAGA | 16924 |
| rs49784652 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74669003 | CAAGGTATCCAGAGG[A/G]AGCCGAATAGCTGAG | 16924 |
| rs49785405 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74613664 | CTCCGGGATTGAGAA[A/G]GCTGCTGGCAGTGCT | 16924 |
| rs49787244 | snp | A/G | 0.231111 | 0.249285 | missense | Lnx1 | GRCm38.p3 | 5:74685777 | TCATCTGCAAGGTCC[A/G]GTTGGTTCATGGCTG | 16924 |
| rs49787961 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74597058 | ATTGAATTAAAAATA[C/T]ATAAACTTAAAAGAC | 16924 |
| rs49790045 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74695401 | CAAACACAGTGGTGA[C/T]GATAAAAGGACAGGG | 16924 |
| rs49794344 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74687496 | AGGAAGGAGACAGTC[G/T]AACAGAAAACCAGGC | 16924 |
| rs49796058 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74613871 | CCCAAATGCTGGCTC[A/G]ACAATGAAGCGTTGG | 16924 |
| rs49800435 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Lnx1 | Mm_Celera | 5:74660219 | ACGAATCAGGGTTCA[C/T]CTCTGTAAAAACAAA | 16924 |
| rs49805187 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74683341 | CCTTTGATGTTGGTT[A/G]GGTGCCTCCCAGCTA | 16924 |
| rs49818535 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74612208 | TTTTGACTCCGTCCC[C/T]ATGAATGGGATCCCT | 16924 |
| rs49822072 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74649075 | CCATCTGTCCCTGGT[A/G]TGCAGTAAAGACACC | 16924 |
| rs49827067 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74667664 | TCCTAAATGGGAGAA[A/G]AGATCCTTAGGCTGC | 16924 |
| rs49827757 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74696251 | GTCCTTCCAGCTGTC[C/T]TTGTAAGTAGTCCAG | 16924 |
| rs49833529 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74662100 | CAAAAAAAAAAAAAA[A/C]CCTCTAAAACAAGGT | 16924 |
| rs49842241 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74701898 | GGGTCTCTCAGGCTC[A/G]TTGAGAGCAGGTTAT | 16924 |
| rs49854327 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602768 | CACACAGGAAATGCC[A/G]GTGTGGCATACTAAG | 16924 |
| rs49858189 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656250 | TGAATTTCTACTCCA[C/T]GGCACACAATGGAAC | 16924 |
| rs49864330 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74605253 | TAAATAAATAAGAAC[A/G]ATCTCTACCTTCAAG | 16924 |
| rs49869802 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74671644 | CACTAACTCACAAAA[A/G]AGAACTTGTGGATTA | 16924 |
| rs49876488 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74629145 | GAACATGTTTCCTTG[A/C]CACTGGGCCAATCAT | 16924 |
| rs49885925 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74614957 | TCACGTGGAGAACCT[A/G]ACATCTTTCTGTTTC | 16924 |
| rs49887139 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Lnx1 | Mm_Celera | 5:74644907 | AGGGACTTCTGAGTT[A/G]CTCAAGTAAAACTTT | 16924 |
| rs49887724 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611945 | GGTAGCTCCTCTCCT[C/T]GTTTCAGTTCCTGAC | 16924 |
| rs49888802 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74658148 | GCCCAGATGTACCAG[C/T]GCTGGATCAGATCTC | 16924 |
| rs49890860 | snp | C/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656488 | CAGTTGAGAGATGCC[C/T]GAGAAAGGGCCTTTT | 16924 |
| rs49898911 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683874 | AGAATGCACTCATGT[C/T]TCAGAAGACAAAGCC | 16924 |
| rs49899783 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74614911 | CTTTTCCTGGATCAT[C/T]GTCAGCTCCCCTTTA | 16924 |
| rs49901299 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74669295 | GTTGGTAATTGTGAA[A/G]TGTGTTATTTTACAA | 16924 |
| rs49904491 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74614290 | ACAGTGGCTAGGAGG[A/G]CAATGATATTACAGG | 16924 |
| rs49905275 | snp | A/G | | | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74653045 | CGTCCTGGAACTCAT[A/G]TTATAGATCAGGTTG | 16924 |
| rs49914587 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74644964 | ACCAGGCTGTGAAGC[A/G]GCATGGTGTTAGCAT | 16924 |
| rs49919187 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74659399 | ATTGCATATGTTCTT[C/T]TAGCATTCTTTCCAT | 16924 |
| rs49922565 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74671596 | GAAGAGCATTTTATA[C/T]CAGACAGTGAAGAGT | 16924 |
| rs49932913 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602538 | AGCTTGCTTTGAAGA[A/C]CTTCCAGATGCAGAA | 16924 |
| rs49937264 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651783 | CAAGGACATGGTGTC[C/T]AGCTAAGGAAGAGGA | 16924 |
| rs49941479 | snp | A/G | | | upstream-variant-2KB, intron-variant | Lnx1, Gm15984 | Mm_Celera | 5:74703152 | CCCGTGTACAGATCT[A/G]AATGCGAATGCCTGA | 16924 |
| rs49946565 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74640880 | CTGATAAGCAAGAGG[C/T]GCTTGGAACACAAGA | 16924 |
| rs49959790 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74672001 | CCCAAACTGATCTTT[A/T]CCCTTGTTGGAACAT | 16924 |
| rs49960748 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Lnx1 | Mm_Celera | 5:74612899 | CCGAGCAGCCCAAAC[A/C]TTCCTTACACTGATA | 16924 |
| rs49962473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681153 | GCCACTAAAGGCTCA[C/T]AACCAAAACATCAAG | 16924 |
| rs49969057 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74611442 | TGTGAAGAAGTCCAC[A/G]TCATGCAGTCGTGCC | 16924 |
| rs49983075 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74638774 | GGTAGGTTCCATGCC[A/T]TGTCCCTGTAACATG | 16924 |
| rs49998240 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74648260 | AGATTTTGGGGCTCT[C/T]GGTGGCAGGGCGGTA | 16924 |
| rs50009838 | snp | C/T | 0.426035 | 0.177515 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656498 | ATGCCCGAGAAAGGG[C/T]CTTTTAAGGAACTGC | 16924 |
| rs50019033 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646031 | TCTTGCTCAAGTGCA[C/T]GGGGCCAAGCAACCA | 16924 |
| rs50023960 | snp | G/T | 0.124444 | 0.216185 | missense | Lnx1 | Mm_Celera | 5:74685665 | GTGGCATATGAGGTC[G/T]TCATCTACATCCTCT | 16924 |
| rs50029924 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74680326 | TCACAGAGAAAGGAG[C/T]TTCAGTTGAGGAAAT | 16924 |
| rs50032347 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653469 | CATGGTGGCACATGC[A/C]TCTAATCCTAGCTCT | 16924 |
| rs50034490 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74671530 | ACAGTTGGCCAAACC[C/T]TGAGTAGAATCTTGA | 16924 |
| rs50035367 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74652258 | CAGGGCGCTAGGCAG[A/G]GACTTGATGAACAGA | 16924 |
| rs50036100 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74673208 | TAATCTCATAGTTAT[A/G]TGTTCTAGTAACCAT | 16924 |
| rs50039026 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74683326 | ATTCAGCCCAGACAG[C/T]CTTTGATGTTGGTTG | 16924 |
| rs50051097 | snp | A/C | 0.497778 | 0.0332592 | intron-variant, utr-variant-5-prime | Lnx1 | Mm_Celera | 5:74697223 | GGGAATGTGCCCCTG[A/C]TCATGTCTCCATTTC | 16924 |
| rs50053437 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | GRCm38.p3 | 5:74616723 | CAGTGACACACTCAA[C/T]GTAAGAATCTGGTGC | 16924 |
| rs50058122 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Lnx1 | GRCm38.p3 | 5:74691962 | GCTGTGCTGAGTCAC[A/G]TCACAGCCTGAGGTG | 16924 |
| rs50058593 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74673462 | TGCCTACTTCAGTTC[A/G]GCAACTTCAGAGCTG | 16924 |
| rs50087231 | snp | A/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646069 | AAGTCTGAAATGGGG[A/T]GCGATGATTGTTCCT | 16924 |
| rs50091864 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74615867 | TGGCTGGGGTGTAGA[A/G]TTGGACCAAGACAAT | 16924 |
| rs50125605 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74690629 | GGGATTATCCATGGA[A/G]CTCTTTAGTGCTTCA | 16924 |
| rs50136647 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74670932 | GAAATATAATAAAAT[A/G]GTAGAGAAAATTAGA | 16924 |
| rs50138788 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74645731 | GATAAACAGTCCCTG[A/G]AGCTTAAGTTAGTGT | 16924 |
| rs50144820 | snp | G/T | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74691393 | AGGTCTGTGGACGTG[G/T]TTGAGAAGACGGAAA | 16924 |
| rs50150317 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697269 | CTAGAATTGAAAAAA[A/T]TAAATGAAGTTGTTT | 16924 |
| rs50150509 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654243 | GGCAGAATAGAAAAC[A/G]CTTTTTGCCTCGGTT | 16924 |
| rs50152919 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74673661 | ATCCCTCAACCACTA[C/T]CTGGTGAGTAGAACT | 16924 |
| rs50154847 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74664381 | CCTCTTTCCTCCCTA[A/G]AATGATACAGCAAAG | 16924 |
| rs50171602 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694274 | GGTACTGATTATGAA[C/T]GGAGATACATTATTC | 16924 |
| rs50187201 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74697454 | ATTTTGGGATGGCAG[C/T]CACTAAGACTCCTGT | 16924 |
| rs50202264 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74660086 | TGCACAAAAAAAATC[C/T]GCTCCGGCAGTTTAC | 16924 |
| rs50203396 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74699224 | ATGTGAGAGCCTCTG[C/T]AGCCCTAAGCAAAGT | 16924 |
| rs50223462 | snp | C/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74643574 | TAAAAATTCCATCTT[C/T]CCAAACAGTTTCTGT | 16924 |
| rs50225139 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74596959 | AAATGCCCATAATAT[A/G]CTCTGTCTTCAACTC | 16924 |
| rs50231057 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74614890 | TCTGCTCAGCCACTC[G/T]TAAGACTTTTCCTGG | 16924 |
| rs50233958 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74691479 | GCGTTAAAATCCACA[C/G]TTTTCCGTTAACTCT | 16924 |
| rs50241792 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74690773 | GTGGGTTTCCTACAG[G/T]GCCTGCAAAGAGCAA | 16924 |
| rs50247567 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74642439 | AGAGATGTCAAGACA[A/G]TTTATCCATCCTAGG | 16924 |
| rs50249715 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74670972 | TTATTTGATGACAAG[A/G]AATTATAGGTCCCCG | 16924 |
| rs50260020 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74613857 | TTTCTCACTGGGCTC[C/T]CAAATGCTGGCTCGA | 16924 |
| rs50264605 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74617162 | GGCTTGGGTTCTACA[C/T]GAGCTGTGCTGATTT | 16924 |
| rs50275093 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74634047 | AGTTTGCAAATATCC[C/T]AAGGGGGGTGTCCTT | 16924 |
| rs50301072 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Lnx1 | Mm_Celera | 5:74645276 | GTGGGTGCATGAGCA[A/G]TTCATGGGTTTTCTG | 16924 |
| rs50303571 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, utr-variant-3-prime | Lnx1, Fip1l1 | Mm_Celera | 5:74597904 | AGCTGTGTTCCTTCG[C/T]AGTATCACATCTTTA | 16924 |
| rs50306864 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Lnx1 | Mm_Celera | 5:74640636 | CATCATCAACAGTTG[A/G]GGCAACTCACACTGA | 16924 |
| rs50308356 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74686163 | AATTGAACCTGATGT[C/T]TCTTCATTACCTTTC | 16924 |
| rs50328845 | snp | C/T | | | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74702748 | TTGTTCAGATCCCTT[C/T]TGGGCCAGAGGTCTA | 16924 |
| rs50342244 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74635934 | ACTAAGCCTACTCTC[C/T]TCCCTCTGGTTTGTA | 16924 |
| rs50366951 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74699084 | GTCGTAATTGTTTGG[A/G]AACACTGTCAGAGGA | 16924 |
| rs50378086 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74632591 | GTCAGTAAACACAAT[A/G]CAATGCTTCTAACAG | 16924 |
| rs50381252 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700809 | ACTGACAATTAATTA[C/T]AGTAATAAGAGCCGG | 16924 |
| rs50381591 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74698090 | CCCACAACCAACCAC[A/C]GGGAATGTGGCCCAC | 16924 |
| rs50394653 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74602109 | CTTCCAACTCACTAA[A/T]GCATCATGATTGAAA | 16924 |
| rs50396986 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651984 | ACACTTGACATCCCC[A/C]AAATGGGTCCTAAGC | 16924 |
| rs50397390 | snp | A/G | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654402 | AACTCAGTGGCTTGT[A/G]TGCTTAAGAAAGGGG | 16924 |
| rs50403644 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74692837 | CAGTGGGAACTTTGT[C/T]GTATGAGGACACCAG | 16924 |
| rs50405686 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74607124 | TGCATGTATTTGAGA[A/G]ACTTTTTTCTGTCTT | 16924 |
| rs50419232 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74672787 | AAGACACTTGGTGGG[C/T]GAGCAGCGTCCCTGT | 16924 |
| rs50430727 | snp | A/T | | | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74648695 | CACGCTCAGCTTATG[A/T]AGTGCTAGTGACCAA | 16924 |
| rs50436352 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74695429 | GGGAGCAAGAGAACC[A/G]CATAGTCAGGCCCAG | 16924 |
| rs50439402 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650213 | TATACGTTCAGAGAA[C/T]TTGCTAATTCCCAGG | 16924 |
| rs50441523 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74671404 | CCACCAGAGCAAGTT[A/T]AAAATGAAGGCGAAA | 16924 |
| rs50449733 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74684812 | TGAATTAGAGAGATG[A/G]TTTACTTATAGAAGG | 16924 |
| rs50459492 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Lnx1 | Mm_Celera | 5:74660113 | TTACCTCACAGACTT[C/T]TGCCAAGTTCAGGGT | 16924 |
| rs50459825 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74687438 | TAGAGTTGTGGCATA[C/T]ACTCCCATGTGCTCT | 16924 |
| rs50466220 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74673983 | TCCTGAGAGCCCACC[A/C]GTTCTCAGGCCCCTG | 16924 |
| rs50471728 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74674181 | GTGCCAAGGGCAGAG[C/G]CCAGACTCTGAACAC | 16924 |
| rs50474764 | snp | A/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74655244 | AGCTTGTGAAAACAG[A/G]AGCCAGGCCCCTACT | 16924 |
| rs50474998 | snp | A/G | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74683687 | AAAGGTCACTAACAC[A/G]CACCCGCACCACCAT | 16924 |
| rs50479343 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74684647 | GCTAGAATGAAGGGT[A/G]ATATTTTTCTGACTT | 16924 |
| rs50502627 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | Mm_Celera | 5:74616929 | CAACGGGGTGACCGG[A/G]CCCCTTAACACTTGG | 16924 |
| rs50511096 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700472 | GGTAGAAGATGTTTG[A/C]CTATGAGATTAGAGG | 16924 |
| rs50516794 | snp | A/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654768 | GTGTGTGCACGTCAC[A/G]TTCCACTTCCCTAGG | 16924 |
| rs50526957 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Lnx1 | Mm_Celera | 5:74685644 | CAGCAATGCTTGCAG[A/G]CAGATGTGGCATATG | 16924 |
| rs50531232 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Lnx1 | Mm_Celera | 5:74613757 | CTTATCAGAAACGTG[A/G]ACGCTGGAGGATCCC | 16924 |
| rs50543140 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74671355 | GACCCAGAAGTTCTT[C/T]ATTTTCTTTTTTCCT | 16924 |
| rs50550484 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74669180 | CTCTCTAGTAAAGCA[A/G]GGAAGGAGGGGCCGT | 16924 |
| rs50553623 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Fip1l1, Lnx1 | Mm_Celera | 5:74592355 | TAAGTTTAATTAGTT[A/G]GTAATTCATATACAG | 16924 |
| rs50567786 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74699272 | CCTTAGGGGTGCAGA[A/G]CTCTCATAGTAACAG | 16924 |
| rs50571616 | snp | G/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74680816 | GTGAACTCCTACCTA[G/T]ACTGTGGACAGCCAG | 16924 |
| rs50574795 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638512 | ACAGCAAAAACCTCA[C/T]GCCTTGTTAATGGAG | 16924 |
| rs50587423 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74682597 | CTCCAGCCATCAGCC[C/T]CATCACACCTTAGAG | 16924 |
| rs50590394 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74682771 | GATAAGAAGGCAGGC[C/T]CAGGGTTAGCTCTGA | 16924 |
| rs50593621 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lnx1 | GRCm38.p3 | 5:74670945 | ATGGTAGAGAAAATT[A/G]GAACTGACTGGTTAT | 16924 |
| rs50597426 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74614117 | GAGAAACAACAGTCC[C/T]GGGCACGAGAGTCTC | 16924 |
| rs50601712 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651362 | TCTTCTTCCATGCCC[A/G]TCTCTGTTCCTTGGT | 16924 |
| rs50617659 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74680332 | AGAAAGGAGCTTCAG[C/T]TGAGGAAATGCCTCC | 16924 |
| rs50618054 | snp | A/T | 0.32 | 0.24 | intron-variant | Lnx1 | Mm_Celera | 5:74695474 | CACCTAGTTCCTAGG[A/T]AGGGTCACAAAAGAG | 16924 |
| rs50618677 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74680291 | CTAGTTTTGTGTCAA[C/T]TTGACACAGGCTGGA | 16924 |
| rs50627567 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74692111 | AGTGGTCAGCTTCAC[A/C]GTCACCATGGTAACA | 16924 |
| rs50637209 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74644044 | GCACTTGTTGAAGGG[C/T]GATGTGGGAATATTG | 16924 |
| rs50658881 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lnx1 | Mm_Celera | 5:74614370 | TCCAGCCAAGGAATT[A/G]CCCTAACTGTAAGGA | 16924 |
| rs50668059 | snp | A/C | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646707 | TTTAATGAGCACTGG[A/C]TCTGAAGACCGGCTC | 16924 |
| rs50682167 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74695786 | GGCCCTATATGACTT[A/G]AAAACATTCTTTTAA | 16924 |
| rs50699508 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74612763 | ACTAGGACACCACTT[C/T]TCTCACCGTCCTCTC | 16924 |
| rs50704181 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lnx1 | Mm_Celera | 5:74630609 | ACATGGTCAGCTCTC[A/G]GGATATAGAAGCCAT | 16924 |
| rs50706855 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74664227 | ATTTGGAAATGAGAG[C/T]GTTGGCCACGAACTC | 16924 |
| rs50707043 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74617257 | TTGAATGTTTAAATC[C/T]CCACAAGAGTTGTGC | 16924 |
| rs50730857 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74613728 | CAGTGAGCAGAGCCC[A/G]CTCTGAGCAACACCT | 16924 |
| rs50743283 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lnx1 | GRCm38.p3 | 5:74683739 | TGGGGAAAGCATTTA[C/T]TACAAACCTACGCTG | 16924 |
| rs50747218 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74665197 | AAAGTGACAAGTGAC[C/T]GGTCAGCCTCGGGCT | 16924 |
| rs50776958 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593330 | ATGTTAGAAAATGTG[C/T]TCTAATGAGTTCCAG | 16924 |
| rs50781036 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Lnx1 | Mm_Celera | 5:74637661 | GGGAACTGCAGGATG[C/T]GCCCACACAGCCCTG | 16924 |
| rs50802425 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74609759 | CTACTGGAAGCTGTT[C/T]GTCATCATGACAGAA | 16924 |
| rs50808845 | snp | C/T | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74656339 | TAACAAGCCAAGAAA[C/T]GTTTCTATAGTCCTA | 16924 |
| rs50812660 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74652938 | TAGGCCCATTAGTTA[C/T]GGACCCTCAAGGATG | 16924 |
| rs50832731 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74662523 | TCGACTTAGGAACAG[C/T]TGGAAAAATTGGGAA | 16924 |
| rs50843038 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Lnx1 | Mm_Celera | 5:74641612 | GTTGGAAGCCAGACA[C/T]AGTATTGGGATTCTT | 16924 |
| rs50852064 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74684832 | CTTATAGAAGGATTT[C/T]TTTGGGCTCATGGTT | 16924 |
| rs50857601 | snp | A/C | 0.32 | 0.24 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653387 | AATTGTAAGACACAA[A/C]GTTTCATACAGGCAT | 16924 |
| rs50860990 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74643273 | TGGAGATAGACATGG[A/G]AGAAGGTGACATGGC | 16924 |
| rs50861584 | snp | C/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74640487 | TGGCTAGTCTCTGAA[C/T]GGGGCCAGTTTCTAT | 16924 |
| rs50870237 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Lnx1 | Mm_Celera | 5:74663162 | GGATATTATTAAGAA[C/T]ACAAGGCCCTGTGAT | 16924 |
| rs50881404 | snp | G/T | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74692769 | GGTGGGCTCACAAGA[G/T]GGATGTGATAACAAG | 16924 |
| rs50883719 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74694952 | TGTCCTCTCACATCC[G/T]AGCTATAAACATGGA | 16924 |
| rs50891294 | snp | A/G | 0.32 | 0.24 | intron-variant | Lnx1 | GRCm38.p3 | 5:74611934 | ATATAAGGTCTGGTA[A/G]CTCCTCTCCTCGTTT | 16924 |
| rs50891705 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Lnx1 | Mm_Celera | 5:74640469 | GTATGCCTGAGATAC[A/G]GTTGGCTAGTCTCTG | 16924 |
| rs50943584 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74610883 | TTCGTTTTGACTTTT[A/G]TTTAATGGAAAGTCA | 16924 |
| rs50951810 | snp | A/G | | | intron-variant | Lnx1 | Mm_Celera | 5:74662519 | AGCATCGACTTAGGA[A/G]CAGCTGGAAAAATTG | 16924 |
| rs50952241 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74614600 | TAGCCAGCTTCTGTG[A/G]GTTCACCTGCTGTCT | 16924 |
| rs50958436 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74671017 | TAGTGTTGTGGACAC[A/G]TTTCTTCACGATTGG | 16924 |
| rs50958741 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Lnx1 | Mm_Celera | 5:74640285 | AATTTTCAAACAAGC[C/T]GAGAAGCCATGTGAG | 16924 |
| rs50964828 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74594621 | GATGCAAGTTGTACT[A/G]TGTCTGCTGGTAAAA | 16924 |
| rs50967346 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74682629 | CAAAGAGATACTTGC[C/T]TCCTGGTCACCCGAG | 16924 |
| rs50974933 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74602255 | GCTCAGAAGAGACCC[C/T]GGGCTTACTCGGGGC | 16924 |
| rs50975218 | snp | C/T | | | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74653044 | CCGTCCTGGAACTCA[C/T]GTTATAGATCAGGTT | 16924 |
| rs50985397 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | GRCm38.p3 | 5:74681948 | ACAATGGACCATGTA[A/C]ATGGCAGATTTAAGA | 16924 |
| rs50988803 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Lnx1 | Mm_Celera | 5:74664689 | TTGAGGAAAAGACTG[C/T]GCTTTCCCCAAGGTT | 16924 |
| rs51006271 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fip1l1, Lnx1 | Mm_Celera | 5:74593083 | GCCAGAAAAGCAGAA[A/G]GTAGAGGAGTTCTCT | 16924 |
| rs51026142 | snp | A/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646906 | ACTTAGTGTACACTC[A/T]GATCCCTCTTCTTAT | 16924 |
| rs51027007 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650614 | AGGCAGGGATAGCCT[A/G]GTCTAACCTGGTAAG | 16924 |
| rs51032627 | snp | G/T | | | intron-variant | Lnx1 | GRCm38.p3 | 5:74670981 | GACAAGAAATTATAG[G/T]TCCCCGTCTGTGTGT | 16924 |
| rs51036147 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700822 | TACAGTAATAAGAGC[C/T]GGGTTCTGAACCAGT | 16924 |
| rs51038653 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74659373 | AGCAATTGCATAGCA[C/T]GGGCTGGTTCATTGC | 16924 |
| rs51060391 | snp | C/T | | | intron-variant, nc-transcript-variant | Lnx1, Gm32304 | Mm_Celera | 5:74654185 | CTCCAGGAATATTGA[C/T]GGGGTAGGTGGTGGT | 16924 |
| rs51068313 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651478 | TCATCCATACATTTC[C/T]ATGTCTCTGTAGAGT | 16924 |
| rs51092931 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681830 | CTTATAGAACGTGAT[A/C]CAGCTGTACCCCAGA | 16924 |
| rs51099147 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74667876 | ATCTTCATCCTTCAA[A/C]CTGGCTTGATCTGGT | 16924 |
| rs51101966 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604937 | CCAGGTGGCACGCAG[G/T]AGAAGCGAGGAACCA | 16924 |
| rs51102297 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74686447 | AATGGAGTTTCAGTT[C/T]CCACAGGAGAATCTT | 16924 |
| rs51104455 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74681896 | GTGAAACAGGCAGAA[A/G]ACGTTCACAAGCCCT | 16924 |
| rs51118964 | snp | C/T | | | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74645748 | GCTTAAGTTAGTGTG[C/T]GTGTGTGTGTGTGTG | 16924 |
| rs51126858 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74662981 | AATCAGTGACTGATG[C/T]ATGCTGTGGTGGGTT | 16924 |
| rs51130191 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74602225 | TCTCCTTCTGAGTCA[C/T]AGAGAGCATGTGACG | 16924 |
| rs51143304 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1, Gm32304 | Mm_Celera | 5:74646774 | GTCTGCATGGCTTGA[C/T]GCTTCCAGAACGCTT | 16924 |
| rs51150673 | snp | C/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74696959 | ACAGCCATGGTTCTC[C/T]CCAGATCTAGGAAGC | 16924 |
| rs51151930 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Lnx1 | Mm_Celera | 5:74678830 | ATGGCTAATCTCACC[A/G]AGGCCTGAATTGAAC | 16924 |
| rs51174699 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74670920 | CAAACTGCCATAGAA[A/G]TATAATAAAATGGTA | 16924 |
| rs51182828 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | Mm_Celera | 5:74604578 | TAGGCTTGGGCCTCA[A/G]ACTACAGCCAAGCCT | 16924 |
| rs51183323 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74635899 | TGGCTCTGCTCACCC[A/C]TCCATGGCCTTGTGC | 16924 |
| rs51187711 | snp | A/C | | | intron-variant | Lnx1 | Mm_Celera | 5:74662089 | GGAGAAACAAACAAA[A/C]AAAAAAAAAACCCTC | 16924 |
| rs51222598 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74638321 | ACTATGTCTGTTTAC[C/T]GTGTGCTTTAGATAT | 16924 |
| rs51233202 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700689 | ACTCTGCTTCGCCAA[A/G]GGGGCTGGCAGACCA | 16924 |
| rs51236257 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lnx1 | Mm_Celera | 5:74680995 | GTGGGGCTTGAGCCG[A/C]CTGAATCATGTTCTC | 16924 |
| rs51236855 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Lnx1, Gm32304 | GRCm38.p3 | 5:74651448 | ATGAAAGCCACTCAA[C/G]TACTATCTTTACTAT | 16924 |
| rs51237162 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Lnx1, Gm15984 | Mm_Celera | 5:74700647 | GAGCCTTGAGCTGGG[A/G]ACAAGAAGGAAGAGC | 16924 |
| rs51240801 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74608191 | TTCTGACAACAGTAG[A/G]CCAACTTCTCAGAAC | 16924 |
| rs51245415 | snp | A/T | | | intron-variant | Lnx1 | Mm_Celera | 5:74617017 | TCCCGCTCTCTCAAG[A/T]CAATGGGGGAATTTT | 16924 |
| rs51246265 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lnx1, Gm32304 | Mm_Celera | 5:74650909 | ATAGATTGTTCAGGC[A/G]ACAAAGGAAAAGACT | 16924 |
| rs51253585 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lnx1 | GRCm38.p3 | 5:74638177 | GAAACACAGGGTGGT[A/G]AAAGAAAGTATAGCC | 16924 |