| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs263303400 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39131718 | GGCAGTAAAAGACAA[A/G]AGAACACTGCAGCAT | 223499 |
| rs263377061 | in-del | -/AA | | | intron-variant | Dcaf13 | Mm_Celera | 15:39126009 | ATCAGACAGATAGTG[-/AA]AGAGTGATTTTTACC | 223499 |
| rs263486819 | in-del | -/C | | | intron-variant | Dcaf13 | Mm_Celera | 15:39131319 | TTAGAGGACGTGATA[-/C]TCTTGCAGAGGAATT | 223499 |
| rs263487799 | in-del | -/TT | | | intron-variant | Dcaf13 | Mm_Celera | 15:39126544 | GGTGGTTTTCAAAGC[-/TT]TTTTTTTTTTCTTTT | 223499 |
| rs263490260 | snp | A/C | | | intron-variant | Dcaf13 | Mm_Celera | 15:39131121 | ATCAGATAAAATTTA[A/C]AAACCAGAGAGGTTA | 223499 |
| rs263601282 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39126752 | TATGGTACCTGGATC[C/T]GTGAATAAGGAAAAA | 223499 |
| rs263634981 | snp | G/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39118918 | ATGGAGAGGCAAGTT[G/T]AAAATCTTGTTTTAA | 223499 |
| rs263680163 | snp | A/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39134632 | AGCAAATTATTAAGT[A/T]AAGGTCCTCAAGAAT | 223499 |
| rs263698249 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39125202 | TTAATAGGAAGTTAC[C/T]ATGTTAATTTCTGTA | 223499 |
| rs263791602 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39144809 | CTGTACCCTGTGCCT[C/T]GTGTGCTCAGCCTCC | 223499 |
| rs263823672 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39135119 | GGGAACTGTGTGTCA[A/G]TGCTCCGCCCCGCAG | 223499 |
| rs263847057 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39128325 | ATTAGTTTGAGTCTT[C/T]GCTTAGACAAGTACT | 223499 |
| rs264006389 | in-del | -/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39133742 | TTTTTTTTTTGGGGG[-/T]GGGGGGGGAGTCCAG | 223499 |
| rs264031720 | in-del | -/AAAT | | | intron-variant | Dcaf13 | Mm_Celera | 15:39117601 | AGAAACCCTGTCTCA[-/AAAT]AAACAAACAAGCAAA | 223499 |
| rs264036485 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39118561 | GTTTGTAAGTGACTA[A/G]TGTACTTTTGTATCT | 223499 |
| rs264051987 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39130910 | CAGTGATGACCATGT[A/G]GTCAGACTGTCTGCT | 223499 |
| rs264088132 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39123056 | TTTATGTATTTGTTA[C/T]AAATTTTTGTTATGC | 223499 |
| rs264090258 | in-del | -/TGT | | | intron-variant | Dcaf13 | Mm_Celera | 15:39141967 | GACTATTTTGAAGGA[-/TGT]TGTTTCCCTAATTTC | 223499 |
| rs264206994 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39126220 | TGATAAAAGCACATG[C/T]CTCTTACCCTGTATT | 223499 |
| rs264247706 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39130377 | ATATAATGTATTTCA[C/T]TTGGTAAATAAGCTT | 223499 |
| rs264276232 | snp | C/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39122252 | CTAAGGCTGAAATTA[C/G]TAGCCAGCTGCCATG | 223499 |
| rs264312893 | in-del | -/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39137813 | GAGCCATCTCACTGG[-/T]TTTTTTGTTTGTCTC | 223499 |
| rs264355749 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39139881 | ATTTAATCACTTAGG[A/G]CCACCTATCCAGGGA | 223499 |
| rs264444216 | snp | A/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39134927 | TTTTCTATGAGTTGT[A/T]TATGCATAAGCAATT | 223499 |
| rs264458655 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39116575 | GAGGGTCCTCCCACC[C/T]CTTACCTCCCTAGGT | 223499 |
| rs264513448 | snp | A/C | | | intron-variant | Dcaf13 | Mm_Celera | 15:39131789 | GTTGTTTCCCCAGAT[A/C]ATCTCTTTTCAGAGC | 223499 |
| rs264643150 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39122491 | GCTAGGATTAAAAAG[C/T]GTGTTCCACCACATT | 223499 |
| rs264664233 | snp | A/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39144728 | GGTTACATACTTTTT[A/T]AAAAATTTTTATGTA | 223499 |
| rs264801159 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39128813 | GAATGAAATTAGTGT[A/G]TTCACTATTAATTAA | 223499 |
| rs264920726 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39120609 | GACTCACTACAAGTT[A/G]TTTCTGTGAAGCTGA | 223499 |
| rs265040261 | snp | C/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39127005 | GAAAATAAGGGGATG[C/G]ATGGGTAGGGGGACT | 223499 |
| rs265068621 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39139811 | AAAAGCAGAGGCCAT[A/G]GAAGAATGCTGTGCA | 223499 |
| rs265104620 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39142331 | CTGGGTGTGTCAGAG[C/T]TCTTGGCAGTCAGGC | 223499 |
| rs265121000 | snp | C/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39130678 | TGACAAGACCAGCAG[C/G]TATGGAGGTGCATAT | 223499 |
| rs265132283 | snp | A/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39116196 | CTTTCAGCTGTTTGT[A/T]GGGGCTTTTGGAGAG | 223499 |
| rs265228159 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39146370 | TTAAAGTCCTGTATC[A/G]CCACACCTGGCTCAA | 223499 |
| rs265256985 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39118378 | CAGATACTGTGCTGC[A/G]CATAGGAGTGCAACT | 223499 |
| rs265274234 | snp | C/T | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | Mm_Celera | 15:39113433 | CCCTAGCATTGCTAA[C/T]GTGTGGTATATGGCC | 223499 |
| rs265293065 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39120198 | ACCACATTTCTTAAC[C/T]CATTCATTTATCAAT | 223499 |
| rs265310682 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39114882 | TTGGAAGTGGATACA[A/G]CGATTATGATTTAGA | 223499 |
| rs265446315 | snp | C/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39139072 | CTGAGAAGGAGTCTC[C/G]ACAGACATAAATAAA | 223499 |
| rs265568864 | snp | C/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39127692 | AACACACGGTTATTA[C/G]TGGAGATTGAACCAT | 223499 |
| rs265618499 | snp | C/T | | | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39111672 | ATACATCAAGTAAAT[C/T]GAATAAAATTAGAAT | 223499 |
| rs265718936 | in-del | -/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39118249 | AGTTATGTTCTATAG[-/T]TAACGCCACAGTGTT | 223499 |
| rs265726607 | snp | A/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39136792 | TCTGCAAAAGCTGAT[A/T]ATTCTGATAGAAAGT | 223499 |
| rs265936591 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39126896 | GGTGGGATGCCTGTA[A/G]CCTACATTAGGGGTG | 223499 |
| rs265953322 | snp | A/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39119545 | TCATTTATTTGTTCC[A/T]AGGACCTTTGGAGCG | 223499 |
| rs266134708 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39129636 | ATTATTGTTATTGTT[A/G]TTATTATTATCGCTA | 223499 |
| rs266154128 | in-del | -/TA | | | intron-variant | Dcaf13 | Mm_Celera | 15:39119799 | GGACTTACTGGAAAG[-/TA]TGTGCACAGGGAAGA | 223499 |
| rs266171987 | snp | C/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39131280 | AAAATTTGACCACCA[C/G]GGGCTGGAGAGATGG | 223499 |
| rs266189541 | snp | C/T | | | intron-variant | Dcaf13 | Mm_Celera | 15:39123650 | TTTCTCTCTTGTTTA[C/T]ATCATCATAGATCTT | 223499 |
| rs266198592 | in-del | -/C | | | intron-variant | Dcaf13 | Mm_Celera | 15:39120905 | GCTAAGGCTTATGTT[-/C]CCCCAGTTGGCATTC | 223499 |
| rs578317354 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133096 | GAGCCTTAGAAAGAT[A/G]TTTTTGGTTGTAACT | 223499 |
| rs578491974 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141676 | AGAAGAGTTTTTGCT[A/G]TCCTAGTTTTTTTGT | 223499 |
| rs578498834 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116386 | GAGCAATTCTGGGTA[A/G]GAGTTTTTGACTGTG | 223499 |
| rs578513287 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132166 | AAGAGAAGAGTGGCT[A/T]GGCGGTGTGAGAGAA | 223499 |
| rs578532868 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134883 | ATTTAATAAATGTCT[A/C]AAAACTGCCTTCTTA | 223499 |
| rs578643116 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141914 | CAGATCTTTCATTTA[C/G]TTAGTTAGAGTCATA | 223499 |
| rs578660652 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133033 | CTCCCGTGGGTGCTG[A/T]CACGACCCACACCTG | 223499 |
| rs578702179 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116384 | AGGAGCAATTCTGGG[C/T]AGGAGTTTTTGACTG | 223499 |
| rs578704928 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140646 | GGCTATTATAAATAA[A/G]GCTGCTATTAACATA | 223499 |
| rs578708112 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136594 | ATAATCCAGGGGTCC[A/T]GTAGTAGGGTGACCA | 223499 |
| rs578713065 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133611 | TGAAAATAACAGTCG[C/G]CACCTGTACGCTCTT | 223499 |
| rs578716145 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132726 | TAAGAATTTGAAATG[A/C]ACTTTATTATGAATA | 223499 |
| rs578728638 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136295 | CCTTCTCTGGTATGA[A/G]TTTCCTTTAATTATT | 223499 |
| rs578730518 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135469 | CTTATGCCACGTGTC[A/G]GAAGACATTAAACTT | 223499 |
| rs578744634 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145704 | CTTGGGGGGGGAGGG[A/G]GGAAAGCAAATCAGT | 223499 |
| rs578753259 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39121873 | CACAGTGAGAAGATG[A/T]TCTTGTAGGAGGGCT | 223499 |
| rs578881269 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145701 | GCTCTTGGGGGGGGA[A/G]GGGGGAAAGCAAATC | 223499 |
| rs579044562 | snp | A/G | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | GRCm38.p3 | 15:39113459 | TGGCCCCCCCCCCCA[A/G]CTCCCAAGGTGTTTT | 223499 |
| rs579067565 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136175 | TAGCTTCTGAGAGCT[A/T]CAGCTAACCACCTGT | 223499 |
| rs579074967 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132685 | AATTTTAAATAGGGC[A/G]TTGGAACCCTGGCAA | 223499 |
| rs579245886 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133789 | CAAATTAGCAAGGCA[C/G]AAGCCAAGTCTCTGG | 223499 |
| rs579247974 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145331 | CTGTCATCACCATCA[C/T]CAAGCAGACACTTTC | 223499 |
| rs579257473 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134897 | TCAAAACTGCCTTCT[A/T]AAAAGGACAGCATTT | 223499 |
| rs579260986 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132637 | TCTGACTTTATAATG[C/T]TAACTAGTACTGAAT | 223499 |
| rs579266756 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135976 | AAGACACAAAAGGGG[A/G]CAGAGTACTTCTGCT | 223499 |
| rs579286941 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140667 | TATTAACATATTGGA[A/G]CATGTGTCCTTATTA | 223499 |
| rs579292846 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116119 | TCCAGCTTTTCCCTA[A/T]TTCAAACACAGGGGT | 223499 |
| rs579298385 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39125872 | TTTAAAATAAGTGAT[G/T]ATATCTCTGATTGTA | 223499 |
| rs579299175 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132179 | CTTGGCGGTGTGAGA[A/G]AAAGATGGAGCTAAG | 223499 |
| rs579300590 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141821 | ATTAATCCTGCCAGT[C/T]CATGAGCATGGGAGA | 223499 |
| rs579301543 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136538 | ATTTTACTATTCCTA[C/T]ACTCAGTTATGAAGG | 223499 |
| rs579344923 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133011 | TGGGTGGAAATTGAC[C/T]CCATTCCTCCCGTGG | 223499 |
| rs579434064 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132269 | GAGGGGCCGATTCCC[G/T]CCAAATAATCCAGGG | 223499 |
| rs579455253 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142157 | CCTTGGTTTATGTTG[C/T]TTCTGTTCTTATGCT | 223499 |
| rs579472384 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116533 | GTCCTGAGAATCTCT[C/T]ACCTCCCAGGTCTCT | 223499 |
| rs579489898 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133264 | TGCACAGTTCTGAGT[A/G]CTGTGCAGCTCCTAA | 223499 |
| rs579520228 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135166 | CATGGGCCAACGATC[A/G]GCTGGGAGGATGAGA | 223499 |
| rs579748923 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133216 | CTGCACCAAGTGGTA[A/C]CCATACTGTATTTGT | 223499 |
| rs579775123 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39137303 | CTTCTCCTCATGGTC[A/C]CTACCTGAGACCCCT | 223499 |
| rs579789021 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116472 | TTCTCCATCATAGTT[C/T]CCTCTCTCCATCATA | 223499 |
| rs579939618 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132259 | GAAGGAGGGGGAGGG[C/G]CCGATTCCCGCCAAA | 223499 |
| rs579968602 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134293 | AGATCCTTTTACGAT[A/G]CTATAAAGCATTTAT | 223499 |
| rs579973099 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39129099 | GTGGTACCTTGCAGT[A/T]CATTTATATATATAT | 223499 |
| rs579979032 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140855 | CACATCCTCACCAGC[A/T]TCTTCTGTCACCTGA | 223499 |
| rs579993967 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39126464 | TTTAGAAATTGACCC[G/T]GGTCTTTACTAAAGG | 223499 |
| rs580035047 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133815 | TCTGGGCTGGTTTTA[C/G]AATAGTAAAAAGGCC | 223499 |
| rs580056235 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39114980 | GAAAGGCTGCTGCAT[A/T]GGAGGAAATGCAAGG | 223499 |
| rs580067538 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141231 | AATTTGTCAATTCTT[A/G]ATCTTATAGCACAAG | 223499 |
| rs580090618 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136446 | CTGGAAAGGCATCTT[A/G]GAAACCTGGAAGAGA | 223499 |
| rs580305547 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134361 | AAAGGTAAGATTTAA[A/G]TAGTGTGCATGGGAA | 223499 |
| rs580311698 | snp | C/T | | | downstream-variant-500B | Dcaf13 | GRCm38.p3 | 15:39146942 | CACTGATCTAAGAGC[C/T]AGCTGTGCAGTAGCA | 223499 |
| rs580358911 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39130802 | CCGGAAAACATTGTT[G/T]GAGAACAAACAAATA | 223499 |
| rs580380329 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141359 | GAGTTCTTGATCTAC[A/T]TAGACTTGAGCTTTG | 223499 |
| rs580409709 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136407 | GTTGTGTCCGGCCAG[C/T]AGATCATATGTCTGG | 223499 |
| rs580416214 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116418 | GATGGCAACCCCATC[C/T]CTCAACTTGATGCCC | 223499 |
| rs580445196 | snp | C/T | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | GRCm38.p3 | 15:39114533 | CCACCACCACCCGGC[C/T]ATTTTTATTTTTATA | 223499 |
| rs580452325 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132784 | TTGGATGACAGGCGG[A/G]GTACAGGGAGGAGGG | 223499 |
| rs580455071 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133131 | ATAGATACCAACCTC[C/T]ATCCAAACCTGGTGT | 223499 |
| rs580494056 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132294 | CCAGGGGTCCAGTAG[C/T]AGGGTGACCACATGT | 223499 |
| rs580500252 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136613 | GTAGGGTGACCACAT[A/G]TATGGCTCCAGAGCA | 223499 |
| rs580521282 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142352 | GCAGTCAGGCTTCCT[C/T]TGAGCCTCTGAGATC | 223499 |
| rs580530951 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132369 | GCAGAACGATTGAGC[A/G]GCAAGCTCCACCCCT | 223499 |
| rs580539927 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142196 | ACCATCTGATTATCT[C/T]AAGTGCTCCCTGCCC | 223499 |
| rs580578236 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135837 | AGCTCTCGGCTTTGC[A/G]GATAAAGTTTTTATG | 223499 |
| rs580759633 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141683 | TTTTTGCTATCCTAG[G/T]TTTTTTGTTATTCCA | 223499 |
| rs580831835 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135938 | TTGAACACGAGAACA[A/G]ATTGGTGCACCAGAC | 223499 |
| rs580964949 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39115209 | AAACAAACAAACAAA[A/C]AACCCAACTGAACCA | 223499 |
| rs580999346 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39120513 | GATGACCCTGGATGA[C/T]AGTCATTCCTGTCAT | 223499 |
| rs581005903 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142257 | TGTAATCCCAGTTGA[G/T]TCAGATCTCCTCAGA | 223499 |
| rs581012840 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135758 | CCCTTTTTTTCTAAA[A/T]CGAACAGTTTTTCCA | 223499 |
| rs581020997 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132317 | CCACATGTATGGCTC[C/T]AGAACAGCAAAGCGG | 223499 |
| rs581060353 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136474 | AGAAGAGTGGCTTGG[A/C]GGTGTGAGAGAAAGA | 223499 |
| rs581093263 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133012 | GGGTGGAAATTGACC[C/T]CATTCCTCCCGTGGG | 223499 |
| rs581098641 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141567 | GATCTACTTGTCTAT[A/C]GCTTTACCAGTACCA | 223499 |
| rs581134665 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132960 | GTGATTAAATGATTT[C/T]CTCATCTGTAGATGA | 223499 |
| rs581175935 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132103 | TTGTCTCCGGCCAGC[A/G]GATCACATTTCTGGG | 223499 |
| rs581177086 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134400 | ATAGTATGTACGGGG[A/G]TTTAATTTTTCTCTT | 223499 |
| rs581187393 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116376 | TTTTAGGCAGGAGCA[A/C]TTCTGGGTAGGAGTT | 223499 |
| rs581199474 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141625 | GTACAGCTTAAGGTT[A/G]GGGTGGTGATTCCAC | 223499 |
| rs581207694 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134487 | CTTGTTGACAAAACA[C/T]TTTAAATACTTGGCT | 223499 |
| rs581275737 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39131568 | GGCTGCTTTCACCCA[G/T]GAACTGAAGCTCTCA | 223499 |
| rs581279404 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133438 | TGCAGTAACACTAAG[C/G]GTGGAAAACCAGAGG | 223499 |
| rs581298397 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136586 | CCCGCCAAATAATCC[A/T]GGGGTCCAGTAGTAG | 223499 |
| rs581356054 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140451 | TTACCAGAGATTGGA[A/G]TAATTTTAAAATCGT | 223499 |
| rs581544580 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133154 | CCTGGTGTATCTCAC[A/G]AGGAACCCAGAAATG | 223499 |
| rs581634957 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39119932 | TCCACTTTCAGAGTG[C/T]ACCTGTGTATTCATT | 223499 |
| rs581639452 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39139071 | GCTGAGAAGGAGTCT[C/T]CACAGACATAAATAA | 223499 |
| rs581640182 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39115894 | CAACCCCATCAGACC[C/T]CCCTACTCCCTGGGG | 223499 |
| rs581654745 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136511 | TAAGACAGTCATCCT[A/G]ATCAAAGCTCAATTT | 223499 |
| rs581664371 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132968 | ATGATTTTCTCATCT[A/G]TAGATGACTGGGCTT | 223499 |
| rs581664770 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132749 | TATGAATAACACTGA[A/G]TGGATATTCCTCCAC | 223499 |
| rs581711790 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133344 | CATTAGTAACACCAC[A/G]ATTTGGGGCTAAAAT | 223499 |
| rs581754683 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145705 | TTGGGGGGGGAGGGG[A/G]GAAAGCAAATCAGTT | 223499 |
| rs581759990 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39126017 | AGATAGTGAGAGTGA[C/T]TTTTACCTTTTGGAA | 223499 |
| rs581797062 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145352 | AGACACTTTCCTTCC[A/G]TCTTACTGTTTGGAA | 223499 |
| rs581822482 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134889 | TAAATGTCTCAAAAC[C/T]GCCTTCTTAAAAGGA | 223499 |
| rs581836726 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140655 | AAATAAGGCTGCTAT[G/T]AACATATTGGAGCAT | 223499 |
| rs581840021 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136018 | AGAGAACAAAGCATG[C/G]CACTCCTGAAATTTC | 223499 |
| rs581842859 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133650 | GGATGCACGGGCTGC[A/G]GTCAGGCTGGAGGAT | 223499 |
| rs581844833 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39122622 | CGGCATCTGTGAGCC[G/T]TCTGATAAGGAAACC | 223499 |
| rs581848072 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132641 | ACTTTATAATGTTAA[C/T]TAGTACTGAATAGGT | 223499 |
| rs581872134 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136399 | CGCCAAATGTTGTGT[C/T]CGGCCAGCAGATCAT | 223499 |
| rs582024772 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136611 | TAGTAGGGTGACCAC[A/G]TGTATGGCTCCAGAG | 223499 |
| rs582029027 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116394 | CTGGGTAGGAGTTTT[G/T]GACTGTGGGATGGCA | 223499 |
| rs582031214 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133097 | AGCCTTAGAAAGATG[C/T]TTTTGGTTGTAACTG | 223499 |
| rs582148258 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136595 | TAATCCAGGGGTCCA[G/T]TAGTAGGGTGACCAC | 223499 |
| rs582324490 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141859 | ATCTTCTGAGATCTT[C/T]GTCAATTTCTTTCTT | 223499 |
| rs582328399 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133037 | CGTGGGTGCTGTCAC[A/G]ACCCACACCTGTGGC | 223499 |
| rs582356999 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135142 | CCCCGCAGCAGCTAG[C/T]TGGGCCCACATGGGC | 223499 |
| rs582363587 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132262 | GGAGGGGGAGGGGCC[A/G]ATTCCCGCCAAATAA | 223499 |
| rs582403618 | snp | C/T | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | GRCm38.p3 | 15:39113660 | TTATAGTGCTTGGCC[C/T]AGGGAGTGGCCTTGT | 223499 |
| rs582449544 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134974 | ATAGCATCTGAGGGA[C/T]GAACAATCTCAAGCA | 223499 |
| rs582453399 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132231 | CAATTTTACTATTCC[G/T]ATACTCAGTTATGAA | 223499 |
| rs582535715 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132702 | TGGAACCCTGGCAAA[A/G]GTTGACTGTAAGAAT | 223499 |
| rs582549264 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140859 | TCCTCACCAGCATCT[G/T]CTGTCACCTGAATTT | 223499 |
| rs582603927 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136226 | GTGCCTCACTGCTGA[A/T]CCTAAGTGAATTAGC | 223499 |
| rs582627262 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133908 | GGAATCTCTAATATT[A/G]GACTGAATATTAGAC | 223499 |
| rs582634982 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145702 | CTCTTGGGGGGGGAG[A/G]GGGGAAAGCAAATCA | 223499 |
| rs582703643 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140796 | CCAGAGTGGTTGTAC[C/T]AGCTTGCAGTCCCAC | 223499 |
| rs582718600 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39125996 | CAAAACAGCAGTAAA[C/T]CAGACAGATAGTGAG | 223499 |
| rs582863594 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133794 | TAGCAAGGCAGAAGC[C/T]AAGTCTCTGGGCTGG | 223499 |
| rs582908235 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132964 | TTAAATGATTTTCTC[A/G]TCTGTAGATGACTGG | 223499 |
| rs582932353 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135261 | CCAATGAATATAATT[A/G]ATAACAATTATAAAA | 223499 |
| rs583065682 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136479 | AGTGGCTTGGCGGTG[C/T]GAGAGAAAGATGGAG | 223499 |
| rs583094103 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142168 | GTTGCTTCTGTTCTT[A/G]TGCTTGCCTCCCACC | 223499 |
| rs583107460 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132318 | CACATGTATGGCTCC[A/G]GAACAGCAAAGCGGC | 223499 |
| rs583119933 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134328 | TTCTTTGACATTTAA[A/T]TTTTAAAAATTGAAA | 223499 |
| rs583124462 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39129147 | TATATATATATTATA[C/G]AAGTGAGGTAGGATG | 223499 |
| rs583142723 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132272 | GGGCCGATTCCCGCC[A/G]AATAATCCAGGGGTC | 223499 |
| rs583145422 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141238 | CAATTCTTGATCTTA[C/T]AGCACAAGCCATTGC | 223499 |
| rs583154690 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133284 | GCAGCTCCTAAAGGA[C/G]AATTGTCAACCTCAG | 223499 |
| rs583182761 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39138311 | TTTGGGTGATACTTA[A/G]TCTTGATGATCATGT | 223499 |
| rs583276641 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135760 | CTTTTTTTCTAAAAC[A/G]AACAGTTTTTCCAGC | 223499 |
| rs583289477 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39137432 | ACATTGGTCAATACA[A/G]TGTCCAGACTGCAAC | 223499 |
| rs583348001 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142344 | AGTTCTTGGCAGTCA[A/G]GCTTCCTCTGAGCCT | 223499 |
| rs583476013 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133229 | TAACCATACTGTATT[C/T]GTATGATCACAAACC | 223499 |
| rs583483679 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136466 | CCTGGAAGAGAAGAG[G/T]GGCTTGGCGGTGTGA | 223499 |
| rs583516897 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116497 | ATCATAGGGCATTTC[A/G]TCTAAGGTCCCTCCC | 223499 |
| rs583525155 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39114981 | AAAGGCTGCTGCATA[A/G]GAGGAAATGCAAGGT | 223499 |
| rs583669369 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141464 | AAAATGTTCTCTTCT[G/T]TCCACTGGATGGTTT | 223499 |
| rs583681966 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132873 | AAGGGCTTGCCCTTC[A/C]AACAGTACAGTCTCC | 223499 |
| rs583724246 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132306 | TAGTAGGGTGACCAC[A/G]TGTATGGCTCCAGAA | 223499 |
| rs583751688 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142201 | CTGATTATCTCAAGT[G/T]CTCCCTGCCCTCAAT | 223499 |
| rs583754012 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135482 | TCGGAAGACATTAAA[C/T]TTGAGTTATCAATTT | 223499 |
| rs583849608 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39131521 | TAAAGAGTAAGTGTC[C/T]AGTGTATGTGACAGC | 223499 |
| rs584045935 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134396 | CTAAATAGTATGTAC[A/G]GGGGTTTAATTTTTC | 223499 |
| rs584117707 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132824 | CGGCTCCATAGTACA[A/G]GGCCAATTGGCTTTT | 223499 |
| rs584153779 | snp | A/G | | | downstream-variant-500B | Dcaf13 | GRCm38.p3 | 15:39147111 | CCTGGTTTCCATAGT[A/G]ATATTTTCAGTGTCC | 223499 |
| rs584155555 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136408 | TTGTGTCCGGCCAGC[A/G]GATCATATGTCTGGG | 223499 |
| rs584164792 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132786 | GGATGACAGGCGGAG[A/T]ACAGGGAGGAGGGGG | 223499 |
| rs584190367 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132162 | CTGGAAGAGAAGAGT[A/G]GCTTGGCGGTGTGAG | 223499 |
| rs584204333 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136599 | CCAGGGGTCCAGTAG[C/T]AGGGTGACCACATGT | 223499 |
| rs584276605 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132391 | TCCACCCCTGAGCAA[A/G]CAGGTTTCAGGCTGA | 223499 |
| rs584284272 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141668 | TATTGTTGAGAAGAG[G/T]TTTTGCTATCCTAGT | 223499 |
| rs584288285 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134531 | GACTAATTGCACTTT[C/T]AATCATTTCTCTTAA | 223499 |
| rs584292815 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140799 | GAGTGGTTGTACCAG[C/T]TTGCAGTCCCACCAG | 223499 |
| rs584371148 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39144894 | TGCTGCTTACCTTCT[A/G]GCATCTGTTTACATG | 223499 |
| rs584463596 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140662 | GCTGCTATTAACATA[G/T]TGGAGCATGTGTCCT | 223499 |
| rs584471888 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133786 | TTGCAAATTAGCAAG[G/T]CAGAAGCCAAGTCTC | 223499 |
| rs584562915 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140599 | TGTATCCATTCCTCC[A/G]TTGAGTGAAATCTGG | 223499 |
| rs584567705 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39121337 | GGAAGCTACAGGGGA[A/C]GAGGCTAAGAAGACG | 223499 |
| rs584570964 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133569 | TCAGACCTAAAAGCC[A/G]CAAAACGTGTTGGAA | 223499 |
| rs584584428 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133433 | GACCTTGCAGTAACA[C/G]TAAGGGTGGAAAACC | 223499 |
| rs584597700 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134997 | CTCAAGCAATTGTGA[A/G]CTCAGAGATATAGCA | 223499 |
| rs584608618 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116379 | TAGGCAGGAGCAATT[A/C]TGGGTAGGAGTTTTT | 223499 |
| rs584715514 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136590 | CCAAATAATCCAGGG[A/G]TCCAGTAGTAGGGTG | 223499 |
| rs584776903 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39139175 | TGAGCCATCCATTTG[C/T]ATATCTCAGTCTGTG | 223499 |
| rs584790653 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141738 | TCTGTGAAGAATTGA[A/G]TTGGAATTTTGATGG | 223499 |
| rs584804212 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132174 | AGTGGCTTGGCGGTG[C/T]GAGAGAAAGATGGAG | 223499 |
| rs584854469 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136033 | CCACTCCTGAAATTT[C/T]TCTCTGCTTTTTGGG | 223499 |
| rs584858274 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132644 | TTATAATGTTAACTA[A/G]TACTGAATAGGTAAC | 223499 |
| rs584859805 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133013 | GGTGGAAATTGACCC[A/C]ATTCCTCCCGTGGGT | 223499 |
| rs584884743 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145678 | GTGCTAGCTGGGTTC[A/G]GTCCTCAGCTCTTGG | 223499 |
| rs584951961 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132028 | ACGGGCCACATGAAG[A/G]TTTCTCCAGGCGACA | 223499 |
| rs584977668 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141592 | GTACCATGCAGTTTT[C/T]ATCACAATTGCTCTG | 223499 |
| rs584983836 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134437 | CTTTTAAGAAGTTTT[A/G]AAGTTTCACAATATC | 223499 |
| rs585055813 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134895 | TCTCAAAACTGCCTT[C/T]TTAAAAGGACAGCAT | 223499 |
| rs585100867 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135165 | ACATGGGCCAACGAT[C/T]GGCTGGGAGGATGAG | 223499 |
| rs585101676 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136536 | CAATTTTACTATTCC[G/T]ATACTCAGTTATGAA | 223499 |
| rs585107766 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132976 | CTCATCTGTAGATGA[C/G]TGGGCTTTTAACCTT | 223499 |
| rs585120230 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39115953 | TTCTCTGACTGAGTC[A/C]AGACCCAGCAGTCCT | 223499 |
| rs585285026 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136404 | AATGTTGTGTCCGGC[C/T]AGCAGATCATATGTC | 223499 |
| rs585299956 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145703 | TCTTGGGGGGGGAGG[A/G]GGGAAAGCAAATCAG | 223499 |
| rs585343799 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132710 | TGGCAAAGGTTGACT[C/G]TAAGAATTTGAAATG | 223499 |
| rs585392962 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132266 | GGGGAGGGGCCGATT[C/T]CCGCCAAATAATCCA | 223499 |
| rs585518195 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116385 | GGAGCAATTCTGGGT[A/C]GGAGTTTTTGACTGT | 223499 |
| rs585574752 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39145706 | TGGGGGGGGAGGGGG[A/G]AAAGCAAATCAGTTG | 223499 |
| rs585605273 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136264 | TTAAACACTGTTTCA[A/G]CTTAGCCCATGCCGA | 223499 |
| rs585633870 | snp | A/G | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | GRCm38.p3 | 15:39114459 | GACCAAGCTGGCCTC[A/G]GAACTCAGAAATCCA | 223499 |
| rs585645372 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134157 | AGGGCACTGAGTTAA[C/T]TTACCTGCCAGCTCA | 223499 |
| rs585650938 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39126934 | GGATCCCAGGGATTC[A/G]CCAGTTAGCTTTTAG | 223499 |
| rs585654822 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133795 | AGCAAGGCAGAAGCC[A/C]AGTCTCTGGGCTGGT | 223499 |
| rs585670732 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39140886 | ATTTTTTATCTTAGC[C/T]ATTCTGACTGGGGTG | 223499 |
| rs585679874 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132781 | TTTTTGGATGACAGG[C/T]GGAGTACAGGGAGGA | 223499 |
| rs585803946 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116471 | TTTCTCCATCATAGT[G/T]CCCTCTCTCCATCAT | 223499 |
| rs585826372 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136797 | AAAAGCTGATTATTC[C/T]GATAGAAAGTAGGCA | 223499 |
| rs585837002 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141942 | ATACCAAAGTGTTTT[A/G]TATTATTTGTGACTA | 223499 |
| rs585840413 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132281 | CCCGCCAAATAATCC[A/T]GGGGTCCAGTAGTAG | 223499 |
| rs585862596 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142181 | TTATGCTTGCCTCCC[A/G]CCATCTGATTATCTC | 223499 |
| rs586097625 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39114977 | CTAGAAAGGCTGCTG[C/T]ATAGGAGGAAATGCA | 223499 |
| rs586174018 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133155 | CTGGTGTATCTCACA[A/G]GGAACCCAGAAATGG | 223499 |
| rs586209261 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132233 | ATTTTACTATTCCTA[C/T]ACTCAGTTATGAAGG | 223499 |
| rs586215837 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135356 | AATAAAGAGACATTG[C/T]TTTAAATCTTATCTT | 223499 |
| rs586230886 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141875 | GTCAATTTCTTTCTT[C/T]AAAGACTTGAAGTTC | 223499 |
| rs586313422 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136612 | AGTAGGGTGACCACA[C/T]GTATGGCTCCAGAGC | 223499 |
| rs586359072 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116413 | TGTGGGATGGCAACC[C/T]CATCCCTCAACTTGA | 223499 |
| rs586396527 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39130793 | GGGATTCTACCGGAA[A/G]ACATTGTTTGAGAAC | 223499 |
| rs586442543 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132950 | CTTAACTGAGGTGAT[C/T]AAATGATTTTCTCAT | 223499 |
| rs586501186 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136414 | CCGGCCAGCAGATCA[C/T]ATGTCTGGGTTCTAG | 223499 |
| rs586509890 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132816 | GTTATGACCGGCTCC[A/G]TAGTACAGGGCCAAT | 223499 |
| rs586608104 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135816 | TTCCTGGTTGAAGCA[A/C]GTGGCAGCTCTCGGC | 223499 |
| rs586719798 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136508 | AGCTAAGACAGTCAT[C/T]CTGATCAAAGCTCAA | 223499 |
| rs586725846 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132967 | AATGATTTTCTCATC[C/T]GTAGATGACTGGGCT | 223499 |
| rs586731691 | snp | C/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141325 | CCTCTATAAGTTTCA[C/G]TGTCTCTGGTTTTAT | 223499 |
| rs586778797 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134337 | ATTTAAATTTTAAAA[A/T]TTGAAAATAAAGGTA | 223499 |
| rs586816007 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136471 | AAGAGAAGAGTGGCT[A/T]GGCGGTGTGAGAGAA | 223499 |
| rs586826469 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39115188 | GTGTGGATTTTCTAT[C/T]TTTAAAAACAAACAA | 223499 |
| rs586918809 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39139269 | CTTATTATAACTCAG[G/T]ATAGCATGTGTTATA | 223499 |
| rs586932587 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132051 | AGGCGACAGGGATCC[C/T]TCTGTGCTGTCTGTT | 223499 |
| rs586970526 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39137861 | ATTGTTGTTTTTCTT[A/G]GTTTTTGTTTTTTTG | 223499 |
| rs586976796 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133240 | TATTTGTATGATCAC[A/G]AACCAGTATGCACAG | 223499 |
| rs586995404 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39116506 | CATTTCGTCTAAGGT[C/T]CCTCCCTTTGAGTCC | 223499 |
| rs587000816 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142349 | TTGGCAGTCAGGCTT[A/C]CTCTGAGCCTCTGAG | 223499 |
| rs587009467 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132356 | AGCAGAGGGCGTGGC[A/G]GAACGATTGAGCAGC | 223499 |
| rs587034218 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141624 | AGTACAGCTTAAGGT[C/T]GGGGTGGTGATTCCA | 223499 |
| rs587040346 | snp | A/C | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134454 | AGTTTCACAATATCT[A/C]ATCTTTTGAATTAAT | 223499 |
| rs587180837 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39134397 | TAAATAGTATGTACG[A/G]GGGTTTAATTTTTCT | 223499 |
| rs587301031 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133434 | ACCTTGCAGTAACAC[C/T]AAGGGTGGAAAACCA | 223499 |
| rs587339403 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133310 | CTCAGAATTAGCAAG[A/G]CCTAGACAAGAATTA | 223499 |
| rs587387653 | snp | A/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39133108 | GATGTTTTTGGTTGT[A/T]ACTGGAAATAGATAC | 223499 |
| rs587401522 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39142231 | TATATCTGATTGGAG[C/T]CTGTCCTTCCTGTAA | 223499 |
| rs587404741 | snp | A/G | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39135659 | ACAATAATAGAATAA[A/G]AAGCACTTTATTATT | 223499 |
| rs587416549 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39138423 | CTGTATCAAGTTAGG[G/T]CAAATCAGGTGGTTT | 223499 |
| rs587436253 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39132307 | AGTAGGGTGACCACA[C/T]GTATGGCTCCAGAAC | 223499 |
| rs587497315 | snp | C/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39131564 | CACAGGCTGCTTTCA[C/T]CCAGGAACTGAAGCT | 223499 |
| rs587514153 | snp | G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39141561 | TACATTGATCTACTT[G/T]TCTATAGCTTTACCA | 223499 |
| rs864293142 | snp | A/G/T | | | intron-variant | Dcaf13 | GRCm38.p3 | 15:39136623 | CACATGTATGGCTCC[A/G/T]GAGCAGCAAAGCGGC | 223499 |