| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs8168882 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166351371 | AAGCTCCCAAATAAA[C/T]AGTAAGAAGATTGGG | 308864 |
| rs63812083 | snp | A/C/G | 0.459184 | 0.136902 | intron-variant | Fchsd2 | Rn_Celera | 1:166217202 | CCACATGTGGGGCAG[A/C/G]CTCTGAATGGGTGTT | 308864 |
| rs63893471 | snp | A/C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217089 | TTCACATTTTGATCA[A/C/T]CTGTCTTGAGTTTCA | 308864 |
| rs63974023 | snp | A/C/G/T | 0.625 | 0.195256 | intron-variant | Fchsd2 | Rn_Celera | 1:166217100 | GGCGTGAAACATTCA[A/C/G/T]ATTGTGATCATCCGT | 308864 |
| rs64062861 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217179 | AAGATTAAAACAGAG[A/G]CAGAAGGAACACCCA | 308864 |
| rs64722583 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Fchsd2 | Rn_Celera | 1:166217213 | AGAGCCTGCCCCACA[C/G/T]GTGGCCCCTACATAT | 308864 |
| rs64758434 | snp | A/C/G/T | 0.71875 | 0.0826797 | intron-variant | Fchsd2 | Rn_Celera | 1:166217086 | GAATTTTGATCATCC[A/C/G/T]TCTTGAGTTTCATGT | 308864 |
| rs64807109 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166229859 | CTTGCTATTGGACCA[A/C]ATTTGTGTTTATCTA | 308864 |
| rs64890442 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fchsd2 | Rn_Celera | 1:166217232 | GTCCATACATATACA[A/G]CCACCCAATTAGACA | 308864 |
| rs65252575 | snp | G/T | 0.412799 | 0.189727 | intron-variant | Fchsd2 | Rn_Celera | 1:166386572 | CAGCACCAGCATACA[G/T]TGTGGCTCACAACTG | 308864 |
| rs65311830 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217096 | TGAAACATTCAGATT[A/G/T]TGATCATCCGTCTTG | 308864 |
| rs65397757 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Fchsd2 | Rn_Celera | 1:166217181 | GATTAAAACAGAGGC[A/T]GAAGGAACACCCATT | 308864 |
| rs65442824 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217226 | CATGTCGCCCATAAA[C/T]ATACAGCCACCCAAT | 308864 |
| rs65492706 | snp | C/T | 0.0559332 | 0.157601 | intron-variant | Fchsd2 | Rn_Celera | 1:166254853 | GTTATAGAGAAAAAC[C/T]TAATGTTTCCCTAAT | 308864 |
| rs65579742 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217187 | AACAGAGGCAGAAGG[A/C]ACACCCATTCAGAGC | 308864 |
| rs82438206 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rnor_6.0 | 1:166241988 | AAGCAGTATTACAGA[A/G]CAATAGTGATAAAAA | 308864 |
| rs104906279 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166344533 | ATCCTGCCTTTCTTT[C/T]TTTTTTTTTTTTTTC | 308864 |
| rs104907795 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217137 | TCCCTCCCAAGGGTA[C/T]TCTTCTTCCCCTTTT | 308864 |
| rs104908605 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298760 | AAAGAAAAGATATCC[A/G]TTTCACCTTGAAGAA | 308864 |
| rs104923852 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166262785 | TGGATGCCATTGGTG[G/T]GGGCTGCTACCTGAA | 308864 |
| rs104927525 | snp | A/C/G/T | 0.58 | 0.222711 | intron-variant | Fchsd2 | Rn_Celera | 1:166217218 | GCTGTATATGCGTGG[A/C/G/T]CCACATGTGGGGCAG | 308864 |
| rs104931181 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166205929 | CAATTCAGTAATACA[C/T]AAAATAGACAGCCAA | 308864 |
| rs104933226 | snp | A/G/T | 0.625 | 0.125 | intron-variant | Fchsd2 | Rn_Celera | 1:166217123 | TTCACTCCTTCTTTA[A/G/T]AAGGGGAACAAGAAT | 308864 |
| rs104935412 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166233622 | TTTGCCTTAAGGAGT[A/G]TGCAAGACTTTGCTG | 308864 |
| rs104955433 | snp | A/G/T | 0.625 | 0.125 | intron-variant | Fchsd2 | Rn_Celera | 1:166217072 | TGTCTTGAGTTTCAT[A/G/T]TGTTCTAGGCATCTA | 308864 |
| rs104987737 | snp | C/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217211 | TTAGAGCCTGCCCCA[C/G/T]ATGTGGCCCATACAT | 308864 |
| rs104994619 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rnor_6.0 | 1:166181009 | AAACAGAACAAACAT[A/G]CTCAGGCTGGCAGTT | 308864 |
| rs104997246 | snp | C/G/T | 0.65625 | 0.0541266 | intron-variant | Fchsd2 | Rn_Celera | 1:166217125 | GGTATTCTTGTTCCC[C/G/T]TTTTAAAGAAGGAGT | 308864 |
| rs105001158 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217191 | GCAGGCTCTGAATGG[A/G]TGTTCCTTCAGCCTC | 308864 |
| rs105002219 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142642 | AGGAATCCCAGTACT[C/T]TGGAGCTCCAGGACA | 308864 |
| rs105009587 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166233294 | CTAAGGAAGGAAGGG[A/T]AGTGGCTGTTCTCTC | 308864 |
| rs105030951 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166225736 | ACTCTGTTGACATGA[C/T]TCCTCCATCATGTGT | 308864 |
| rs105036585 | snp | A/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217143 | CTCTATTCCCTGCCA[A/T]GGGTATTCTTGTTCC | 308864 |
| rs105062594 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217074 | ATCGGTCTTGAGTTT[C/T]ATTTGTTCTAGGCGT | 308864 |
| rs105065356 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217122 | TTCTTGTTCCCCTTT[A/G]AAAGAAGGAGTGAAG | 308864 |
| rs105077926 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Fchsd2 | Rn_Celera | 1:166217101 | AGGAGTGAAGCATTC[A/G]CATTTTGATCATCCG | 308864 |
| rs105096789 | snp | A/C/T | 0.277778 | 0.248452 | intron-variant | Fchsd2 | Rn_Celera | 1:166217145 | CTCTCTATTCCCTGC[A/C/T]AAGGGTATTCTTGTT | 308864 |
| rs105101644 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166221339 | TTGTCCCATTTCTAG[G/T]TGCAGTAGTTACATG | 308864 |
| rs105110873 | snp | A/G/T | 0.611111 | 0.124226 | intron-variant | Fchsd2 | Rn_Celera | 1:166217127 | CTCCTTCTTTAAAAG[A/G/T]GGAACAAGAATACCC | 308864 |
| rs105112951 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217113 | ATGCGAATGCTTCAC[G/T]CCTTCTTTAAAAGGG | 308864 |
| rs105114726 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162992 | TATTCCTGGTTTCAG[C/T]TTGTGATTTCTGTAA | 308864 |
| rs105141053 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166265739 | TAGCCCGGAAGCTAC[C/T]GGGCTAGGATTTGAT | 308864 |
| rs105145987 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166370897 | GGGAAGGGGGAAACT[C/T]GTACCTGCTAGTGTA | 308864 |
| rs105147376 | snp | A/C/G/T | 0.7 | 0.1 | intron-variant | Fchsd2 | Rn_Celera | 1:166217230 | TGGCCCATACATATA[A/C/G/T]AGCCACCCAATTAGA | 308864 |
| rs105155223 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217109 | TTTAAAGAAGGAGTG[A/G]AGCATTCACATTTTG | 308864 |
| rs105164199 | snp | A/C/T | 0.570312 | 0.160679 | intron-variant | Fchsd2 | Rn_Celera | 1:166217154 | AATCTCTGCCTCTCT[A/C/T]TTCCCTGCCAAGGGT | 308864 |
| rs105165873 | snp | C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217171 | CCTTCTGCCTCTGTT[C/T]TAAATTTTGCCTCCC | 308864 |
| rs105187797 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217189 | AGGCTCTGAATGGGT[A/G]TTCCTTCTCTGTCTG | 308864 |
| rs105197598 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142292 | TCACCCAACTGGGAA[A/T]TTTTACCTTTTTTAC | 308864 |
| rs105203667 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166360869 | GATAAACCACTAATC[C/G]TGTGGAGCCAGGTCA | 308864 |
| rs105223517 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166258857 | TGGTTATGAGTGAAA[A/T]TTTAAAAAAATTACA | 308864 |
| rs105239854 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166163025 | GATGATATCTAAATT[A/C]AATCTGCTTGGATCT | 308864 |
| rs105259696 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217067 | TGAGTTTCATTTGTT[C/T]TAGGCATCTAGGGTA | 308864 |
| rs105264759 | snp | A/C/G/T | 0.62 | 0.1249 | intron-variant | Fchsd2 | Rn_Celera | 1:166217192 | GGCAGGCTCTGAATG[A/C/G/T]GTGCTCCTTCTGTCT | 308864 |
| rs105298442 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166186568 | AGAGCTCATGATTAA[A/T]TTTTAAAATAACACT | 308864 |
| rs105307208 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217214 | GAGTCTGCCCCACAT[A/G]TGGCCCATGCATATA | 308864 |
| rs105317017 | snp | A/G/T | 0.53125 | 0.20492 | intron-variant | Fchsd2 | Rn_Celera | 1:166217087 | CATGAAAGTCAAGAC[A/G/T]GATGATCAAAATGTG | 308864 |
| rs105321349 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166246123 | CAGGGTTCCAGATGG[C/T]CTTTGGCTTTTTCCT | 308864 |
| rs105323177 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217219 | GGCTGTATATGTATG[G/T]GTCACATGTGGGGCA | 308864 |
| rs105326098 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166299218 | AACGATATTTTCTAG[G/T]TCCATCTATTTGCCT | 308864 |
| rs105334998 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166367773 | AATAAAACAGTCCTA[A/G]TCCAGAGTCATAGCA | 308864 |
| rs105335300 | snp | A/C/T | 0.625 | 0.125 | intron-variant | Fchsd2 | Rn_Celera | 1:166217102 | AAGGAGTGAAGCATT[A/C/T]ACATTTTGATCATCC | 308864 |
| rs105342670 | snp | A/C/T | 0.59375 | 0.121031 | intron-variant | Fchsd2 | Rn_Celera | 1:166217098 | AGTGAAGCATTCACA[A/C/T]TTTGATCATCTGTCT | 308864 |
| rs105366080 | snp | C/G/T | 0.623967 | 0.124996 | intron-variant | Fchsd2 | Rn_Celera | 1:166217107 | AGCAAAATGCAAATG[C/G/T]TTCACTCCTTCTTTA | 308864 |
| rs105381094 | snp | G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217066 | GAGTTTCATTTGTTC[G/T]AGGCATCTAGGGTAA | 308864 |
| rs105383719 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217082 | GAACACATGAAACTC[A/T]AGAAGGATGACCAAA | 308864 |
| rs105390356 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166366077 | TGTCAACATGTATAT[A/C]TGTATACTAGAAGAG | 308864 |
| rs105407771 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166312093 | TCTCTGTACCAATAC[A/C]ATGCAGTTTTTATCA | 308864 |
| rs105425371 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166255127 | ACCTGAACGTTTTTG[A/G]TTGGTAAAGTTTACT | 308864 |
| rs105438745 | snp | A/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217193 | GGGCAAGCTCTGAAT[A/G/T]GGTGTTCCTTCTGTG | 308864 |
| rs105439703 | snp | A/C/T | 0.62 | 0.1249 | intron-variant | Fchsd2 | Rn_Celera | 1:166217140 | AGGGGAACAAGAATA[A/C/T]CCTTTGCAGGGAATA | 308864 |
| rs105446232 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217129 | AAGGGTATTCTTGTT[C/T]CCCTTTTAAAGAAGG | 308864 |
| rs105471664 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217203 | ACACTCATTCAGAGC[G/T]TTCCCCACATATGGC | 308864 |
| rs105472511 | snp | A/C/G | 0.277778 | 0.248452 | intron-variant | Fchsd2 | Rn_Celera | 1:166217132 | ACCAAGGGTATTCTT[A/C/G]TTCCCCTTTTAAAGA | 308864 |
| rs105478692 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166299231 | TTACCTCACTCAGAA[C/T]GATATTTTCTAGGTC | 308864 |
| rs105481545 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217055 | GTTCTAGGCATCTAG[A/G]GTAATTCAAGCATTT | 308864 |
| rs105485441 | snp | A/C/G | 0.611111 | 0.124226 | intron-variant | Fchsd2 | Rn_Celera | 1:166217186 | AAACAGAGACTGAAG[A/C/G]AACACCCATTCAGAG | 308864 |
| rs105492950 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166155013 | AAGGACCCTCTAGAG[A/G]AACAGAACTTAGAGA | 308864 |
| rs105504873 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217208 | TATGGACAACATGTG[A/G]GACAGGCTCTGAATG | 308864 |
| rs105505558 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166260087 | CAGAAGAGGAGAAAA[A/G]CATTTTAACCTAGTG | 308864 |
| rs105516671 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Fchsd2 | Rn_Celera | 1:166217141 | GGGGAACAAGAATAC[A/C/T]CTTGGCAGGGAATAG | 308864 |
| rs105527631 | snp | A/C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217104 | AGAAGGAGTGGAGCA[A/C/T]TTGCATTTTGGTCAT | 308864 |
| rs105533827 | snp | A/G | 0 | 0 | upstream-variant-2KB | Fchsd2 | Rn_Celera | 1:166138201 | ACTCGATGTAAAACA[A/G]TTGGGTCCAAGTCCA | 308864 |
| rs105541467 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217194 | GCTGAAGGAACACCC[A/G]TTCAGAGCCTGCCCC | 308864 |
| rs105550289 | snp | A/C/G/T | 0.5 | 0.19839 | intron-variant | Fchsd2 | Rn_Celera | 1:166217106 | AAAGAAGTAGTGAAG[A/C/G/T]ATTCACATTTTGATC | 308864 |
| rs105560038 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166385917 | CGGCCTGTAAGTCTC[C/T]CACCTTGAAGGGTTA | 308864 |
| rs105585784 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217112 | CCTTTTAAAGGAGGC[A/G]TGAAACATTCACATT | 308864 |
| rs105594969 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166187021 | CTCTTCCTCCTCCTC[C/T]TCTTCCTCCTCTTTC | 308864 |
| rs105595342 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Fchsd2 | Rn_Celera | 1:166217217 | CCTGCCCCACATGTG[A/G/T]CCCATACATATACAG | 308864 |
| rs105597425 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166258475 | CCAGCACATACTGAC[A/T]GCACAGTTGACAATG | 308864 |
| rs105606891 | snp | A/C/T | 0.611111 | 0.124226 | intron-variant | Fchsd2 | Rn_Celera | 1:166217242 | ATACAGCCACCCATA[A/C/T]AGACAAGATGGATGA | 308864 |
| rs105607848 | snp | C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217157 | TTGTAATCTCTGCTT[C/T]CCTATTCCCTGAAAT | 308864 |
| rs105644470 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166202040 | ACTTGGATCTACTTG[A/G]GCTTTGTGCATGGTG | 308864 |
| rs105650353 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298639 | TGAAGGTTTTTGAGA[A/C]TCCCAAACACAGGCA | 308864 |
| rs105653517 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217181 | GAATGGGTGTTCCTT[A/C]TGCCTCTGTTCTAAA | 308864 |
| rs105670394 | snp | C/G/T | 0.5 | 0.235702 | intron-variant | Fchsd2 | Rn_Celera | 1:166217147 | GCCTCTCTCTTCCCT[C/G/T]CCAAGGGTATTCTTG | 308864 |
| rs105680101 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166299274 | CAGTTATCAGTTAGC[A/G]TGCCATGTGTGGTTT | 308864 |
| rs105683653 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217166 | GAATAGGGAGGCAAA[A/G]TTTAGAACAGAGGCA | 308864 |
| rs105701312 | snp | C/G/T | 0.46 | 0.245764 | intron-variant | Fchsd2 | Rn_Celera | 1:166217062 | TTCATTTGTTCTAGG[C/G/T]ATCAAGGGTAATTCA | 308864 |
| rs105711019 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166315784 | TACATTACCATTCTA[C/T]TGCAGCAGAATAAGT | 308864 |
| rs105712967 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166150992 | CATTCAAAGCATCTG[A/G]AGATATTTAAATGCC | 308864 |
| rs105719237 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166228340 | TGCAGTATGAAATAG[A/G]TATTGAAATAAACTC | 308864 |
| rs105722607 | snp | A/G/T | 0.666667 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217207 | ATAGGCCACATGTGG[A/G/T]GCAGGCTCTGAATGG | 308864 |
| rs105733880 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217157 | CTTGGCAGGGAATAG[A/G]GAGGCAAAGATTAAA | 308864 |
| rs105749110 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217175 | GGCAAAGATTAAAAC[A/G]GAGACAGAAGGAACA | 308864 |
| rs105749666 | snp | C/G/T | 0.59375 | 0.121031 | intron-variant | Fchsd2 | Rn_Celera | 1:166217101 | AAGGAGTGAAGCATT[C/G/T]GCATTTTGGTCATCC | 308864 |
| rs105758640 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166165046 | CTGCTGTCAAGAAAT[A/G]TAGTCCCTCCTTCCT | 308864 |
| rs105760230 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217125 | TTCACTCCTTTAAAA[A/G]GGGGAACAAGAATAC | 308864 |
| rs105770181 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166299102 | TCTGGGTTCTTTCCC[A/G]CTTCTGGCTGTTATA | 308864 |
| rs105776105 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217241 | TATACAGCCACCCAA[A/C/T]TAGACAAGATGGATG | 308864 |
| rs105796266 | snp | A/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217216 | GCCTGCCCCACAGGT[A/G/T]GCCCATACATATACA | 308864 |
| rs105797029 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166246760 | CAGTTTTACTGAATT[A/C]GATCCACCCATGATT | 308864 |
| rs105806148 | snp | C/G/T | 0.611111 | 0.124226 | intron-variant | Fchsd2 | Rn_Celera | 1:166217135 | CCTGCCAAGAATATT[C/G/T]TGGTTCCCCCTTTTA | 308864 |
| rs105815334 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fchsd2 | Rn_Celera | 1:166217119 | TTGTTCCCCTTTTAA[A/G]GAAGGAGTGAAACAT | 308864 |
| rs105821790 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217062 | TGATTACCCTAAATG[C/T]CTAGAACAAATGAAA | 308864 |
| rs105822576 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166205711 | GCATGGGAGATCTCT[A/C]CATTTTCTGAGATCT | 308864 |
| rs105827305 | snp | A/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217117 | TGTTCCCCTTTTAAA[A/G/T]TAGGAGTGAAGAATT | 308864 |
| rs105828847 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166318198 | CATTTTATATAAATG[G/T]AATCCTATACTATGG | 308864 |
| rs105836456 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217101 | AAGGAGGGAAGCATG[C/T]GCATTTTGGTCATCC | 308864 |
| rs105839915 | snp | A/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217121 | TCTTGTTCCCCTTTT[A/G/T]AATAAGGAATGAATC | 308864 |
| rs105864774 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Fchsd2 | Rn_Celera | 1:166217115 | TCCCCTTTTAAAGAA[A/G/T]GAGTGAACCATTCAC | 308864 |
| rs105895677 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217178 | AAAGTTTAGAACAGA[G/T]GCAGAAGGAACACCC | 308864 |
| rs105897636 | snp | A/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217213 | AGAGTCTGCCCCACA[A/G/T]TTGGCAGATACACAT | 308864 |
| rs105899114 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217239 | TCCATCTTGTCTAAC[A/T]GGATGGCTGTATATG | 308864 |
| rs105900588 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166164721 | TTTCAGTGGGCATGC[A/G]TGCACATCTGTTACC | 308864 |
| rs105900718 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166185066 | TATGAAAGTTCTGTG[C/T]ATGCAGCCTGCTAGC | 308864 |
| rs105905179 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217077 | GCCTAGAACAAATGA[A/C]GCTCCAGATGGATGA | 308864 |
| rs105910692 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217229 | TCTAGTTTGGTGGCT[A/G]CATATGTATGGGCCA | 308864 |
| rs105931723 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166264182 | ATAAGATCATGTTGA[C/T]ATATAAATATTTAGA | 308864 |
| rs105951736 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166264401 | TTTTGTGTTCCCTTT[G/T]ATATATGTTCTCATA | 308864 |
| rs105964014 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166258483 | TACTGACTGCACAGT[A/T]GACAATGTCGACACA | 308864 |
| rs105976828 | snp | C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217147 | TGCCTCCCTATCCCC[C/T]TCTAAGGGTATTCTT | 308864 |
| rs105990870 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162904 | CATGAAACTATATTT[C/T]TCTTCCGTTTTGAAT | 308864 |
| rs106003019 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166389099 | GTTGTTGTTGTTGTT[G/T]TTTTTCCATATGAAG | 308864 |
| rs106016086 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166251004 | CTTTCTCCGCAACAT[A/G]TTAAGATTTATCTTT | 308864 |
| rs106018393 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166354193 | GGAGGGCCCAGGAGC[A/G]GCAGGACCCCTGCGC | 308864 |
| rs106025909 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217074 | TCTGTCTTGAGTTTC[A/G]TTTGTTCTAGGCATT | 308864 |
| rs106027508 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217238 | CATTTACAGCCACCA[A/T]ACTAGATAAGATGGA | 308864 |
| rs106044492 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166392728 | GAACAGTTGGAGGGA[A/G]CCACTGGGATGCTGA | 308864 |
| rs106045114 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217233 | TTGTCTAATTGGGTG[A/G]CTGTATATGTATGGG | 308864 |
| rs106072641 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166233689 | ATGTGAAGGTGTGGA[A/G]CACAGGAAAATATAG | 308864 |
| rs106090773 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166377383 | TCTTTTGGTGGCTGT[G/T]TTTTTTTTTTGAATG | 308864 |
| rs106092521 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166389915 | GTTCGTTTATATGGT[A/T]TATTACATTGATGGA | 308864 |
| rs106111522 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166317721 | CATATTTGCTACTTA[C/T]CTTTTCAGCCTTAAG | 308864 |
| rs106115781 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217238 | CCATCTTGTCTAACA[A/G]GATGGCTGTATATGT | 308864 |
| rs106126753 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142601 | AGAATAGTAAGATGG[A/C]CATGGTGGCATGTAT | 308864 |
| rs106128949 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166219448 | CTAGGGTAGACATTA[A/C]AATGTTTGCTCTTTG | 308864 |
| rs106143812 | snp | A/C/G | 0.666667 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217202 | CCACATGTGGGCCAG[A/C/G]CTCTGAATGGGTGTT | 308864 |
| rs106156082 | snp | C/G/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217112 | AATGTGAATCCTTCA[C/G/T]TCCTTCTCTAAAAGG | 308864 |
| rs106157438 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166168904 | GAGCTTCCATTCAAA[A/C]CAAAACAAAACAAAA | 308864 |
| rs106162967 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298553 | CCTATGTTCTAAAGC[G/T]TTGTGACAAGCTGCA | 308864 |
| rs106166585 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166273814 | TGATTGCTCTGACTA[C/T]GACTTCAAGTACTAT | 308864 |
| rs106197651 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166315114 | ATGGGAGGATGGGGA[A/G]GGGAACACCCATATA | 308864 |
| rs106207830 | snp | A/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217183 | ATAAAACAGAGACTG[A/T]AGGAATACCCATTCA | 308864 |
| rs106208436 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Fchsd2 | Rn_Celera | 1:166217237 | CATCTTGTCTAATTG[A/G/T]GTGGCTGTATATGTA | 308864 |
| rs106217618 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217110 | CAAAAGTGAATGCTT[C/T]ACTCCTTCTTTAAAA | 308864 |
| rs106220987 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142421 | TGAAACTAGACTAGC[A/C]CTGTTTGTTAAAACA | 308864 |
| rs106238202 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166353229 | GGAGGGTGCTGTTAC[C/T]GCATGCTTTTATAAG | 308864 |
| rs106240124 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142518 | CTACTTATATCCATA[A/C]CAAGGGAGACTCTGA | 308864 |
| rs106242055 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162343 | GTTACATGGGTGCTT[C/T]TAAAAAATTAAAAGG | 308864 |
| rs106253712 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217130 | CTTCTTTAAAAGGGG[A/T]ACAAGAATACCCTTG | 308864 |
| rs106255142 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166262392 | CAGCCCCTGCATGCA[C/G]TTTATATGTACAGGC | 308864 |
| rs106257623 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217189 | CAGAGCCTGAAGGAA[C/T]GCCCATTCAGAGCCT | 308864 |
| rs106259480 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162885 | TGGCTTTACTTATTT[A/C]ACACATGAAACTATA | 308864 |
| rs106267712 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217184 | TAAAACAGAGACAGA[A/T]GGAACACCCATTCAG | 308864 |
| rs106297489 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217201 | GAACATCCATTCAGA[A/G]CCTGCCCCACATGTG | 308864 |
| rs106298582 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142559 | TAAGCCATTGCACTA[A/C]CATTGTGAAGATGAA | 308864 |
| rs106310098 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166180565 | TTTAATGGAATTTGA[A/G]TGGTGAACCCTTTCA | 308864 |
| rs106321481 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166337118 | TTGTTCCTTCATAAT[A/G]GTTTTTGACAACTGT | 308864 |
| rs106336225 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166372895 | GTTGATGGGACTTGG[A/G]GGCCTAAGTATCTCC | 308864 |
| rs106339263 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166246014 | ACCTGTGGTCCCGAG[G/T]CTCAGGTTTGCTCGT | 308864 |
| rs106349856 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217220 | GCCCCACATATGGCC[C/T]ATACATATACAGCCA | 308864 |
| rs106353316 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166336234 | TTCTTCCTTCCTCCC[A/T]TCCTCCCTTCTTTCC | 308864 |
| rs106356485 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217205 | ACTCATTCAGAGCTT[G/T]CCCCACATATGGCCC | 308864 |
| rs106357945 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142617 | CATGGTGGCATGTAT[C/T]TGGAATCCCAGGAAT | 308864 |
| rs106378138 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166307176 | CAGCATATTCATATA[C/T]ATTAAATAAATAAAT | 308864 |
| rs106381195 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166207361 | TCCCCTCCCCTCCCC[A/G]TCCCCTCTCTAAATG | 308864 |
| rs106383171 | snp | A/G/T | 0.625 | 0.125 | intron-variant | Fchsd2 | Rn_Celera | 1:166217239 | TCCATCTTGTCTAAT[A/G/T]GGATGGCTGTATATG | 308864 |
| rs106383551 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166325310 | CCCTCTATCCTTGAT[C/T]TCTACAAGACTTTCA | 308864 |
| rs106387180 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142686 | AAGGAAACCCTGTTT[A/C]CAAAAAAAAAAAAAA | 308864 |
| rs106393746 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166337761 | GGTTTAGTCCCTGGG[A/G]GCTCTGGGAGGTCTG | 308864 |
| rs106434799 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217180 | AGATTAAAACAGACA[C/G]AGAAGGAACACCCAT | 308864 |
| rs106439644 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166376557 | CACACACACACACAC[A/G]CACACACACACACAC | 308864 |
| rs106453622 | snp | A/C/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217103 | GATGATCAAAATGCG[A/C/G]ATGCTTCATTCCTTC | 308864 |
| rs106465606 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166163032 | TCTAAATTCAATCTG[A/C]TTGGATCTCATAAAA | 308864 |
| rs106467794 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166225665 | GTTCTTCACCATCTC[G/T]TTAGTCCCAAATTAT | 308864 |
| rs106494741 | snp | A/C | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217190 | AGACACAGAAAGAAC[A/C]CCAATTCAGAGCCTT | 308864 |
| rs106500035 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142289 | TAATCACCCAACTGG[A/G]AAATTTTACCTTTTT | 308864 |
| rs106535868 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166361551 | GAGACAAACAGATCC[A/G]TAGAGCTCACTGGCT | 308864 |
| rs106538611 | snp | A/C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217138 | AAAGGGGAACAAGAA[A/C/T]TCCCTTGGCAGGGAA | 308864 |
| rs106553383 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217111 | CTTTTAAAGAAGGAG[G/T]GAACCATTCACATTT | 308864 |
| rs106556150 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298754 | AAGATATCCATTTCA[C/T]CTTGAAGAAACCCTT | 308864 |
| rs106559329 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166348824 | ACACTTCACAAGTTC[A/G]CTCTTGCCTCGCTTA | 308864 |
| rs106567674 | snp | A/C/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217209 | GTATGGGCCACATAT[A/C/G]GGGCAGGCTGTGAAT | 308864 |
| rs106607557 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166191457 | GATCTCCTTTTGTTG[C/T]TTCCTGAGTCCTGTG | 308864 |
| rs106643128 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217210 | TGTATGGGCCACATG[C/T]GGGACAGGCTCTGAA | 308864 |
| rs106678810 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166299069 | TGAGACTGTTGTGGT[A/G]AGGATGTGGAGAAAG | 308864 |
| rs106697713 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217197 | GAAGGAACACCCATT[A/C/T]AGAGCCTGCCCCACA | 308864 |
| rs106735366 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142392 | AGTGTTTGGGATGAG[C/G]CAGTCACCCCAGATG | 308864 |
| rs106741240 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217221 | GTGGATGTATATGTA[C/T]GGGCCACATGTGGGG | 308864 |
| rs106751232 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166342754 | TCTACTATGTAAGTC[A/G]GGTTAGAAAAGTTGC | 308864 |
| rs106752441 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217145 | ACCAAGAATAACCTT[A/G]ACCGGGAATTGGGAG | 308864 |
| rs106760080 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166353569 | CTGTAGTGTGTCACT[C/T]AGTTCCAGGCACAGT | 308864 |
| rs106771639 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217165 | GCCTCTGTTCTAAAC[A/C/T]TTGCCTCCCTATTCC | 308864 |
| rs106791513 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166172482 | GCTTCCTAGGTAAGC[A/G]CTCTACCACTGAGCT | 308864 |
| rs106829039 | snp | C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217185 | TCTGAATGGGTGTTC[C/T]TTCAGTCTCTGTTTT | 308864 |
| rs106829284 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217073 | CTGTCTTGAGTTTCA[C/T]TTGTTCTAGGCATTT | 308864 |
| rs106847888 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217237 | CATCTTATCTAGTTT[A/G]GTGGCTGTATATGTA | 308864 |
| rs106848030 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166201975 | GCTCTTCCCCACTTT[C/T]TCCTCTATTAGACTC | 308864 |
| rs106849961 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166265810 | GTTCTTTTTAAGATC[A/G]ATTTTTAACTGTACA | 308864 |
| rs106862500 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217204 | ACCCATTCAGAGCCC[A/G]CCCCACATGTGATCC | 308864 |
| rs106862775 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166258851 | ATTCTATGGTTATGA[A/G]TGAAATTTTAAAAAA | 308864 |
| rs106868123 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217093 | ACTCAAGACGGATGA[A/T]CAAAATGCGAATGCT | 308864 |
| rs106878173 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166307442 | AGTGCTAATATCTGT[C/T]GATTAACACATTATG | 308864 |
| rs106887228 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166192490 | CTGTCCCTCTATCCA[C/T]TTATTGTTGTTGTTG | 308864 |
| rs106912633 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166328586 | ATTTGCTTCCTCTTC[A/G]CAGAACCTAAAGTAG | 308864 |
| rs106941382 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217141 | GGGAACAAGAATACT[C/T]TTGGCAGGGAATAGA | 308864 |
| rs106967558 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217224 | TTTAGTGACTGTATA[C/T]ATATAGGCCACATTT | 308864 |
| rs106987300 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166315886 | TTCTCATGCAGTAGT[C/T]AAAGGTCAATAAGTA | 308864 |
| rs107020050 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142548 | AATTTAATAGATAAG[A/C]CATTGCACTACCATT | 308864 |
| rs107033285 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166262234 | ATGGGCACTTTTCAG[C/T]CTTATACACCCTAAT | 308864 |
| rs107045519 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166151794 | TCCCTCCAATGCAGC[G/T]TGAGTACTTAATAAC | 308864 |
| rs107052150 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166272068 | GCATTTGGGCTATTA[C/T]CTGCTTATCAGTGAG | 308864 |
| rs107056428 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166315567 | TACAGCTGTCTCAGT[C/T]TTTAAAAATGGATGA | 308864 |
| rs107081916 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166262965 | TATGTTGATGACTGT[A/G]GTCTGGGCTGCCACC | 308864 |
| rs107091814 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166234877 | ATTATTGCTACATAT[A/G]TATATGTACATATAC | 308864 |
| rs107109216 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166317079 | TACAGAACAGAAGTG[A/G]TAGTCTACCAGCAAG | 308864 |
| rs107110903 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rnor_6.0 | 1:166170585 | TAACCCCAATAAATC[A/T]CTGGTTCACTAAAAG | 308864 |
| rs107121574 | snp | A/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217134 | CTGCCAAGGGTATTC[A/T]TGTTCCCCTTTTAAA | 308864 |
| rs107134776 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166307443 | GTGCTAATATCTGTT[A/G]ATTAACACATTATGT | 308864 |
| rs107136973 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166320268 | TTGCACTTGCTAGGC[A/G]AGCGCTCTACCACTG | 308864 |
| rs107152757 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166312316 | TTTTATGTCATGTAT[G/T]TGTGGTCAGGCGTGC | 308864 |
| rs107161376 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217117 | TCCCTACTCCTTCCC[A/G]AGGAGTGAAGCATTC | 308864 |
| rs107170051 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166392978 | CCCTCAACCCAAGGA[C/T]AGTGACAGGTCCTGC | 308864 |
| rs107176173 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166142335 | TATTTATTGGCTTTA[A/C]CAATTCTATCATGTT | 308864 |
| rs107177829 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166288130 | AAGTGACACCATAAA[A/G]ACAATATGACTCTAA | 308864 |
| rs107216675 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166269731 | TACAGATGGAGTAGA[A/G]ATAGAGAGTAGAAAA | 308864 |
| rs107260800 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166260141 | TTCTTTTCTTTTCTC[A/G]GGAACCCAAACATTA | 308864 |
| rs107281693 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166264714 | TGTCTTTAGACATAC[C/T]AAAAGAGGGATTGGA | 308864 |
| rs107296574 | snp | A/C/G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217081 | AGAACAAATGAAACT[A/C/G/T]AAGACAGATGATCAA | 308864 |
| rs107345453 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166376548 | GCACACACACACACA[C/T]ACACACACACACACA | 308864 |
| rs107371163 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Fchsd2 | Rn_Celera | 1:166217129 | CTTTTTTAAAAGGGG[A/G/T]AACAAGAATACCCTT | 308864 |
| rs107376083 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217114 | CCCCTTTTAAAGAAG[G/T]AGTGAAGGATTCACA | 308864 |
| rs107379842 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166260469 | CACTGCCTGGCCTCA[G/T]TTGAAGGATTCTTAT | 308864 |
| rs107382559 | snp | C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217124 | TATTCTTGTTCCCCT[C/T]TTAAAGAAGGAGTGA | 308864 |
| rs107392211 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298718 | ATTCTTGAGACCTAT[A/G]AAATGAAACGTTTGC | 308864 |
| rs107406387 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166258850 | AATTCTATGGTTATG[A/T]GTGAAATTTTAAAAA | 308864 |
| rs107424998 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166253447 | AGGCTTATGGGGACC[A/G]TATTGATTATGTTGG | 308864 |
| rs107444737 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217179 | ATGGGTGTTCCTTCT[C/G]CCCATCTTTTAATCT | 308864 |
| rs107462924 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166344574 | CTTTTTTCTTTTTTC[C/T]GGAGCTGGGGACTGA | 308864 |
| rs107464406 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166198368 | GCAACATAAAGATGA[A/G]TACTGATGCTCAGCT | 308864 |
| rs107483035 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217058 | TGCTTGAATTACCCT[A/T]AATGCCTAGAACAAA | 308864 |
| rs107526830 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166219826 | GGCAATACTTAAAGC[C/T]TGGGGCACATACAGG | 308864 |
| rs196966870 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166383592 | GGCCCTCTGCTTCAG[A/C]ACAGTGCTCTGCTCA | 308864 |
| rs196970433 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166250267 | AAAATTTTAACCCAG[A/T]ATTGCTCATGTCTAA | 308864 |
| rs196975834 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166249147 | AAAGCTACATATTAA[G/T]ATCTTCACTCACATG | 308864 |
| rs196980759 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166156806 | CCTGACCTGTTGCAC[C/T]GGTGGCTGAGAATGT | 308864 |
| rs196982947 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166219643 | TCTAGCACTGACGCC[G/T]TTCCTTAAGCTGGTT | 308864 |
| rs197004347 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166271595 | ATAGGGTTGCAAACC[C/T]CTTCAGCTATTTCAG | 308864 |
| rs197051191 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166163629 | TGGGAGTTAGACTCA[A/G]GGGCTTGGATTTATT | 308864 |
| rs197053959 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166338828 | TCTTCTCATTAGTCC[A/G]TGAATTTGCATTTAG | 308864 |
| rs197054711 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166184680 | AAACCGAATAACACT[C/T]GAAATGTAAATAAAT | 308864 |
| rs197071889 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166225653 | AGGCCAGTCAATGTT[C/T]TTCACCATCTCTTTA | 308864 |
| rs197096340 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166368102 | ATAAGATATAAGTAC[A/G]CCATTTGCCTTATAT | 308864 |
| rs197106934 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166205798 | TGGTTAGAGTTACCC[C/G]CAAGATATTTTATAT | 308864 |
| rs197149292 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rnor_6.0 | 1:166170636 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 308864 |
| rs197158947 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166232006 | GGCCAGGGTGGTCAG[C/G]CTGTGAGCCCTAGGG | 308864 |
| rs197160546 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162727 | AAGAGAAAGCGAATG[C/G]GGAGGCAGAAATGCA | 308864 |
| rs197165524 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166297778 | AAAGATAGGGCATCA[A/T]GTGAAGGGGTGGCCA | 308864 |
| rs197206714 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166262601 | CATGCATCGTGTGCA[C/T]TGTAGAGAGAGGTGG | 308864 |
| rs197232512 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166331825 | CCGCTAAAGTTAACT[A/G]TAAAGGTTTTGATTT | 308864 |
| rs197258428 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rnor_6.0 | 1:166181807 | GAGAGGAATGTAGGC[C/T]GGAGATGTGGTTTTG | 308864 |
| rs197271599 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166163517 | ATCATGTTGGCCTTG[C/T]ACTTTCTGAGCTCTA | 308864 |
| rs197314820 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298174 | CAGCAAGTCAAAGTC[A/T]AGTTGAAGTTTCAGA | 308864 |
| rs197362080 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217084 | ATTTTGATCATCCGT[C/T]TTGAGTTTCATTTGT | 308864 |
| rs197382166 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166223583 | GGTCGATTTAGCTAC[A/G]TGCCTCTTTAAAAGG | 308864 |
| rs197413882 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166189541 | ACTTCAGTGTTGTCT[C/T]TCTTTATGATTTTTT | 308864 |
| rs197431514 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166350630 | CCGGCCAGAGATATT[C/T]CATTCTTTTGACAAG | 308864 |
| rs197437945 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166175871 | ATATTTCACCTTACT[C/T]GAGACAGTCTGTGTT | 308864 |
| rs197453854 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166377906 | GCTATATGTTGGGCA[A/G]TATATTTTCTAAAAA | 308864 |
| rs197509976 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166155614 | TTTTTTTTTTTCAGT[C/G]ACTGACTACTGCTTC | 308864 |
| rs197522943 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166271364 | GTGCTCCCTCCCCCA[C/T]CTACTCCCTCCTAAC | 308864 |
| rs197529123 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166340439 | CAATAGTGGACTATC[A/G]TATGTTTACCAAAAT | 308864 |
| rs197536144 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217132 | CCTAAGGGGATTCTT[G/T]TTTCCCTTTTAAGAA | 308864 |
| rs197556913 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166330759 | TGTAACCAAAAGACA[C/T]AGTTTGGAATATGAC | 308864 |
| rs197597299 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162721 | ATGGGAAAGAGAAAG[C/G]GAATGCGGAGGCAGA | 308864 |
| rs197627333 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166231865 | TGTGTGTCTGTGTGT[C/G]TGTGTGTGTGTGTGT | 308864 |
| rs197637109 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166330142 | TTCTGTGTCTAAAGA[C/T]AACTGCAGCATGCAT | 308864 |
| rs197646540 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166347098 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 308864 |
| rs197647811 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217093 | TTCAAGAAAGAGGAC[C/G]AAAATGGGAATGCTT | 308864 |
| rs197648427 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166169098 | TCCTTCCTCACCCTC[A/C]CAGGTAACTGGGATT | 308864 |
| rs197671543 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166323093 | AAATATACCCCAGTA[A/C]CTCCAGTGACCTAAT | 308864 |
| rs197680864 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166256776 | TTGCAGGAAGACCAC[A/G]CACATCTCTTTTAAA | 308864 |
| rs197702025 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166155506 | AAATACATGCTTTCA[A/C]ATCATGGTTAGTCAT | 308864 |
| rs197717150 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166147411 | GACTCCAGAAGGACT[C/G]TTTATAGCTCCCCTC | 308864 |
| rs197736475 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166374718 | TCCCAAACCTGTGTG[A/C]CTTCTAGAAATCTAG | 308864 |
| rs197745965 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166218188 | TGCCGAGTCTCTTTC[C/T]CTCTACCCATGGATC | 308864 |
| rs197814878 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | Fchsd2 | Rn_Celera | 1:166141858 | GGCAGGGACAGGAAA[A/G]CTAGAAGTATACAGT | 308864 |
| rs197821945 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162681 | AGCTTGGTCCACATA[C/G]CAAATTCTCTGACAT | 308864 |
| rs197839896 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166209913 | TTTTCTCTTTCATTC[C/T]CTTCTTTCCCTTTCT | 308864 |
| rs197848546 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166188413 | CTTGAGCTTCGTGTG[A/G]TCTGTGGATTATATC | 308864 |
| rs197855299 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166321036 | GTCAAACACTGGAGC[A/G]TCCCGAGTGCCTCTA | 308864 |
| rs197887420 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166256298 | CATGGCAGTAAGCAC[A/T]TTTACCTACTGAGCC | 308864 |
| rs197891622 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166180833 | TTCATTTGCAGTACT[C/G]AAGCTGAAATTGCTG | 308864 |
| rs197902270 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166163183 | ACTTTTGAGACAGTG[C/T]CTCTCATTTAACTTA | 308864 |
| rs197902710 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166324507 | TTGTCATAGTACTAC[A/C]AATTGTGTAGATAAA | 308864 |
| rs197905030 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298512 | AGCTCAGATATAAAG[A/G]AACAAGCAGCATGAA | 308864 |
| rs197922460 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217138 | AAAATGGGAGAAGAA[C/T]ACCCTTGGAAGGGAA | 308864 |
| rs197938059 | snp | A/T | 0 | 0 | upstream-variant-2KB, intron-variant | Fchsd2 | Rnor_6.0 | 1:166140401 | TCCCGCAAGGGGCCA[A/T]GACCACTCTAGCCTC | 308864 |
| rs197958249 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166346417 | CGCTGGCCCCCACAC[A/C]CACATGCACATGGAC | 308864 |
| rs197989942 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166210219 | AAGGAAGTGCTTTGG[G/T]GATTTGGTAAATTAA | 308864 |
| rs198023121 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166336272 | CTTTCACCAAGGAGA[A/G]TGAAAACTGAGTAAT | 308864 |
| rs198029671 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166206622 | GCAAGGCCTTGGGTT[C/T]GGTCCCCAGCTCCTA | 308864 |
| rs198039912 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166187053 | CCTTCTCCTTTTGGT[A/G]GTTTTGGGAATTAAA | 308864 |
| rs198062316 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217207 | TCAGGAACACCCTGC[C/T]GCACATGTGGCCCAT | 308864 |
| rs198073419 | snp | A/G | 0 | 0 | upstream-variant-2KB | Fchsd2 | Rn_Celera | 1:166138477 | AGCCTGGTACTCCTC[A/G]GGTGGTCTGGACAGA | 308864 |
| rs198087255 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166392503 | GTAGTCGGGTGCTCT[G/T]AACCGCTGAGCCATC | 308864 |
| rs198089241 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166364438 | GCACACCTTTAATCC[C/T]AGCACTCAGGAGGCA | 308864 |
| rs198104084 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166166711 | TGACTCTGCATTATC[C/T]AAAGCCTTATCCAGA | 308864 |
| rs198209339 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166333916 | ACACACACACACACA[A/C]GTGGTGACAAGGACA | 308864 |
| rs198221741 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166313126 | GGGACCGAACCCAGG[G/T]CCTTGTGCTTGCTAG | 308864 |
| rs198222894 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166155033 | GAACTTAGAGAATGA[A/G]TGTGTGTGTGTGTGT | 308864 |
| rs198249604 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162878 | GCATATCTGGCTTTA[C/T]TTATTTCACACATGA | 308864 |
| rs198256706 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162675 | GAGGTCAGCTTGGTC[C/T]ACATACCAAATTCTC | 308864 |
| rs198279420 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166166001 | TTGAACTTTGAGGTT[C/T]GTTATAGTAGAGTAG | 308864 |
| rs198304499 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166271090 | AGCTGGGGATCGAAC[C/T]CAGGGCCTTGCGCTT | 308864 |
| rs198344400 | snp | A/C/G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217095 | GAAGCATTCGCATTT[A/C/G/T]GGTCATCCTTATTGA | 308864 |
| rs198380156 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162815 | AAATGATCCTTAGTA[C/G]ACTTGCACAGTCCTC | 308864 |
| rs198392114 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166263223 | TTTTCTGTTTGAACA[C/G]TATGCTGAGCTGGCC | 308864 |
| rs198396536 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166222001 | TTTTACAGTGTATGT[A/G]TATAATCAATCATTC | 308864 |
| rs198401860 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166154888 | TACATTTTTTTTCTT[C/T]TTTTTTTTCTTTTAT | 308864 |
| rs198427345 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166254171 | ACTACCACCACCTGT[A/G]TTACAGAACTGAATC | 308864 |
| rs198429212 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166159198 | TTATCATAATAGGCT[A/T]AGAAATTGTTGGACT | 308864 |
| rs198432416 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217200 | ACATGTGGGGCAGGT[A/T]CTAAATGGGTGTTCC | 308864 |
| rs198436918 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166153809 | ATTTCTCTTGTCAGT[C/T]GTGTGTTATTAACCC | 308864 |
| rs198438311 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166393117 | CCCACCCAGATCTGA[C/T]ACTCTGTATAACCAA | 308864 |
| rs198479231 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217218 | TGCCCCACATGTGGT[A/C]CATACATATACAGCC | 308864 |
| rs198480284 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166260925 | ACATGGTTCTCTAGA[A/G]AATACTAGTTGCAAT | 308864 |
| rs198512930 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298244 | TGTTAGGCAGAGCAT[C/T]AGGTTCAAAGTCGTC | 308864 |
| rs198515632 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298984 | AGGGCAAAATGAATA[C/T]AATTTAAGTATGCTT | 308864 |
| rs198536902 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166206406 | TTGGGTTTATAGCCA[A/G]CTTAATTCCTGGTAT | 308864 |
| rs198547790 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166153009 | TAGAGACTATGTGGG[G/T]TTTTTTTTTTTTTTT | 308864 |
| rs198588872 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166249553 | ATATTATTTTAATCT[A/C]TGTATTATTAATGAG | 308864 |
| rs198605827 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166220080 | TTGTCAGTATCTTAT[A/C]CCCATGGCAATAGTC | 308864 |
| rs198653144 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166371380 | CCTCTCCCCACTGTT[A/G]GGCATTTCATCTAAG | 308864 |
| rs198662101 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166298381 | AGCTATTAGGAGGAA[A/G]GGTTCTCATTGGTGA | 308864 |
| rs198677753 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166272143 | GATGATTATTTTCTA[A/G]TTCCATCCATTTGCC | 308864 |
| rs198724962 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166370825 | AGTCTCTCAAGAGTT[A/G]GGTGCATCTCCCCTC | 308864 |
| rs198728898 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166260059 | TTTCACTTTTGCTGC[A/G]AAGGAAAGGGAACAG | 308864 |
| rs198771531 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166159646 | CTCTTCTACTCCTCT[A/G]TACCAGTGTATGGTG | 308864 |
| rs198774167 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166255948 | TGCTCTCTACCTTAG[A/T]TCAGAGCCTCTCTGA | 308864 |
| rs198810560 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166221442 | TTGATTTTGGGGTGT[A/G]TGTGTGTGTGTGTGT | 308864 |
| rs198818645 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166200811 | ATCAAGTTCTCCTCC[C/G]TACCATCCCCTTTCC | 308864 |
| rs198831727 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166196405 | ACATGGTGCACAGAC[A/G]AACATGCAGGCAAAA | 308864 |
| rs198833201 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217151 | ATTACCCTTGGAAGG[A/G]AATTGGGAGGCAAAA | 308864 |
| rs198836967 | snp | A/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166326031 | TATGAGATCTCTCCA[A/G]TTTCTTTATGGAGGC | 308864 |
| rs198849881 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166288516 | ACACACACACACACA[C/T]ACACACACACACACA | 308864 |
| rs198865339 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166343370 | GTTTCTTCTAAAATA[A/C]GATCTCAGCTTTGTA | 308864 |
| rs198869087 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166206266 | ACTTCCAGGAGCTAG[C/T]TTCTTCCTTTCACTA | 308864 |
| rs198869508 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166185374 | AGGGAACCAAACCCA[A/T]GTCCTCTCTGGAAAA | 308864 |
| rs198873814 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166369496 | AGGAAGAACTGAGTG[A/G]ATGAATGGAAGGACG | 308864 |
| rs198897992 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166258783 | TGTGTGTGTGTGTGT[A/G]TGTGTAATTTGGGAG | 308864 |
| rs198898069 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166297758 | AGGGGTGGCCATCCC[A/T]CAGTCAAAAACTCTG | 308864 |
| rs198911313 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217206 | CCCATTCAGAGCCTG[A/C]CCCACATGTGGCCCA | 308864 |
| rs198947487 | snp | G/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166190158 | CTGGGTACAGAACTG[G/T]CTTTTGTTTTTCAAG | 308864 |
| rs198959568 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166176158 | GGTACTTCTTTGCAT[C/T]ATTATTATTATTATT | 308864 |
| rs198978636 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166237202 | GACTCACTCGTCCTC[C/T]GAGTCAGAAGTCCCA | 308864 |
| rs198980949 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217171 | TCCCTCTGTCTCTGT[C/T]CTAAACTTTGCCTCC | 308864 |
| rs198985000 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166371224 | ACAGGACCTCCTTTC[C/G]CTCAGTCTCTTTTCC | 308864 |
| rs198988057 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166346198 | ACTGAGAGCAGAGAT[A/G]GGTATACGGGAAGGT | 308864 |
| rs198988552 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166314672 | ATGATTAATTGCAGC[C/T]AGATATTTAGAACTT | 308864 |
| rs198989265 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166370713 | ATCTTTTTCCCTCCG[A/G]CAGTTCTTCATCCCA | 308864 |
| rs199013920 | snp | A/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166198963 | CCACCACTCAGCTCC[A/T]ATTTCTGTTTTTAAA | 308864 |
| rs199016001 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166389818 | GAAGACTTAACATGA[A/C]GTGGTATTGGATTTT | 308864 |
| rs199017632 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166332944 | ATTAAAGATGCATCC[C/T]ACTGACACCTGGTTT | 308864 |
| rs199041795 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166195284 | TTACAATTCTATACC[C/G]ACCTAGGTAGAGCAG | 308864 |
| rs199042218 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166220361 | AGAACCAACTACTTT[A/C]CCTCCATATCTGCAC | 308864 |
| rs199048227 | snp | A/C | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166179417 | TTTTCATATATTGAC[A/C]AAACACCAAATACAT | 308864 |
| rs199069934 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166165922 | TAGCTCATTTTTTAT[A/G]CTGGTACAGATTATT | 308864 |
| rs199093587 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166291449 | TTACAAAAAGTAACC[A/C]TGTCCCTTCCTCTGT | 308864 |
| rs199104199 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166185365 | TGTGGGTTTAGGGAA[C/T]CAAACCCAAGTCCTC | 308864 |
| rs199129881 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166194724 | GTCTATAAGGTAGGA[C/T]AATAGGGGCTGGAGA | 308864 |
| rs199134070 | snp | C/T | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166179346 | AATTCTATTACTTTG[C/T]TACATTCTGAAGCTA | 308864 |
| rs199146079 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166353014 | AGAGCTAGTGTTCAC[A/G]GAATCCCAACTTTCA | 308864 |
| rs199153052 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166154217 | CGTGCTTTACATATG[C/T]GAGGAAAGATGAGTG | 308864 |
| rs199158293 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166332293 | GCTGGAGCCATAAGT[C/T]CATCCCTGTGTTCTC | 308864 |
| rs199158541 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162807 | AATATAGAAAATGAT[A/C]CTTAGTACACTTGCA | 308864 |
| rs199173426 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166158245 | TTATTTACTTAATTC[A/C]TTAAAAATTTGAATT | 308864 |
| rs199204375 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166319620 | GCCTCCTGAGTACTG[A/G]GATTAAAGGTGTGCA | 308864 |
| rs199222422 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166206296 | AAGTGAGTCCTGGAG[A/G]TCAGACTCAGGTTGT | 308864 |
| rs199227685 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166186111 | AAGAAACAAATTTGC[C/T]TTAGTCATGTCTTTT | 308864 |
| rs199255921 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217139 | AGGGGGAACAAGAAT[A/G]CCCTTGGCAGGGAAT | 308864 |
| rs199272934 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166370605 | AAAGCTATGCTTCTG[A/C]GTCTGAAGGAAGAAG | 308864 |
| rs199276533 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166345451 | GTATTTGGTGGCATT[C/G]TCTTCTTGGTGTCCA | 308864 |
| rs199364086 | snp | A/C | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166318803 | AAAAAAAAAAAAAAA[A/C]AAACGAAAAAACAAT | 308864 |
| rs199371082 | snp | A/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217214 | GTATATGTATGGGCC[A/G]AATGTAGGGTAGGCT | 308864 |
| rs199384022 | snp | C/G | 0.5 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166217145 | TTTGCCTATTCCCTC[C/G]AAAGGGTATTCTTGT | 308864 |
| rs199389365 | snp | C/T | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166162754 | TGCAAGCATTTTCAG[C/T]GTAATGTAGTAGTAA | 308864 |
| rs199390169 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166174009 | GAGAATTAGCTCAGC[C/G]GTTAACAGCACCGTT | 308864 |
| rs199413962 | snp | C/G | 0 | 0 | intron-variant | Fchsd2 | Rn_Celera | 1:166150706 | TGTTGTAGGGTATCT[C/G]ATGTCCTCCTAAGGC | 308864 |