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 |