SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs342 | snp | A/G | 0.312593 | 0.242037 | intron-variant | ASB4 | GRCh38.p7 | 7:95489283 | CTTATTTGTAATCCA[A/G]TAGCTTTATTCTGTC | 51666 |
rs43060 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471806 | atttgccatgtgcca[C/G]ggacaatgctaagta | 51666 |
rs43061 | snp | C/T | 0.386694 | 0.20932 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473222 | TTCAAGGAGACCTGT[C/T]GGATTGCACTGAATT | 51666 |
rs43062 | snp | C/T | 0.244205 | 0.249933 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473786 | GATGGGGAACAATGG[C/T]CAGGGACTCCAGGCC | 51666 |
rs43063 | snp | C/T | 0.39214 | 0.205661 | | | GRCh38.p7 | 7:95480475 | aggatatgatagaaa[C/T]agtggtatatgactt | 51666 |
rs43064 | snp | G/T | 0.245916 | 0.249967 | | | GRCh38.p7 | 7:95481582 | TTTCTTCCCTATGGT[G/T]GCATTTGATAAGTGA | 51666 |
rs43065 | snp | C/T | 0.288646 | 0.246995 | | | GRCh38.p7 | 7:95481979 | GTGTAATTTGACCTC[C/T]TGAGGTGAGTTGAAG | 51666 |
rs43066 | snp | A/T | 0.245631 | 0.249962 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484880 | TGTAATGGATACCAA[A/T]ATATCCCTTACTAGA | 51666 |
rs43067 | snp | C/T | 0.357664 | 0.225629 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485392 | TCCCCACCTCCTCCC[C/T]TCCCAGCTTTTCATA | 51666 |
rs43068 | snp | A/T | 0.317451 | 0.240729 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485618 | CAGATGTTTTTATTG[A/T]GGGGAAAAAAAGAGC | 51666 |
rs43069 | snp | C/T | 0.243347 | 0.249911 | intron-variant | ASB4 | GRCh38.p7 | 7:95486650 | AATAAATGGATAAAG[C/T]GGTGCCACAGGCACC | 51666 |
rs731910 | snp | A/C | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95514563 | AGGGAGAATTTGTGT[A/C]CCCTGAAGCCAGACA | 51666 |
rs737902 | snp | C/T | 0.222035 | 0.248431 | intron-variant | ASB4 | GRCh38.p7 | 7:95509443 | GTGCTTAGTTTGGAA[C/T]AGAGGATTAATGAGC | 51666 |
rs757035 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95535145 | CTAATGTCTTGGGAT[A/C]ACAGATAAAACAGAG | 51666 |
rs763464 | snp | C/T | 0.280785 | 0.248097 | intron-variant | ASB4 | GRCh38.p7 | 7:95532517 | AGGTAACACGAGGGT[C/T]TGGGAGAGGTAAGGA | 51666 |
rs763465 | snp | C/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95533035 | CCCACTAATCTCTGT[C/G]CCTAACCTTCTCACT | 51666 |
rs1015882 | snp | C/T | 0.40595 | 0.195396 | | | GRCh38.p7 | 7:95467303 | actccaccaacacag[C/T]ttgtgtgaccctgag | 51666 |
rs1015883 | snp | C/T | 0.424659 | 0.17887 | | | GRCh38.p7 | 7:95467335 | aagttacttaatttc[C/T]GAACCCTTATTCCTT | 51666 |
rs1015884 | snp | A/G | 0.407158 | 0.194426 | | | GRCh38.p7 | 7:95467356 | CTTATTCCTTTTCAC[A/G]AAAATAGATGAATTA | 51666 |
rs1034467 | snp | A/G | 0.00676609 | 0.0577691 | | | GRCh38.p7 | 7:95468016 | TCCAGCAAAAGAGAT[A/G]GGTGTCAAACCTCTG | 51666 |
rs1476515 | snp | A/G | 0.499424 | 0.0169631 | intron-variant | ASB4 | GRCh38.p7 | 7:95489949 | TCATACATCTGAAGG[A/G]AGATCAAGTTGGTAA | 51666 |
rs1476516 | snp | C/G | 0.35809 | 0.225425 | intron-variant | ASB4 | GRCh38.p7 | 7:95489898 | TGGACAGTCCTTCGT[C/G]TTTCCAGTATGGAAG | 51666 |
rs1557782 | snp | A/G | 0.36315 | 0.222928 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469845 | ATTTTCCGTTATATC[A/G]GTCTTATCAGATTGA | 51666 |
rs2023780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95527099 | GGTATAGTAGAAATA[C/T]TCATTGAAAGAGAGA | 51666 |
rs2074125 | snp | A/G | 0.494272 | 0.053207 | intron-variant | ASB4 | GRCh38.p7 | 7:95504704 | TTACTGTTACCCTCA[A/G]TGTATGTCAAGGGAT | 51666 |
rs2074126 | snp | C/T | 0.35894 | 0.225016 | intron-variant | ASB4 | GRCh38.p7 | 7:95501460 | AGGTGGTAAGAGCAG[C/T]GTCTGTCCAGCAGGC | 51666 |
rs2078990 | snp | A/G | 0.49334 | 0.057322 | intron-variant | ASB4 | GRCh38.p7 | 7:95506302 | atcaacctgaaactc[A/G]ttggagcaggtctga | 51666 |
rs2079081 | snp | A/G | 0.24449 | 0.249939 | | | GRCh38.p7 | 7:95461293 | TGCAAAGCCACAGAG[A/G]TGAAGCTGCCTAAGG | 51666 |
rs2158047 | snp | A/G | 0.207253 | 0.246318 | intron-variant | ASB4 | GRCh38.p7 | 7:95522627 | GGAGGACCAACACAG[A/G]TAAGTGCTTCCCAAC | 51666 |
rs2158136 | snp | A/T | | | | | GRCh38.p7 | 7:95467490 | GGAGTGGGATAGGGT[A/T]TGCTAGAGGACAGAG | 51666 |
rs2158137 | snp | C/T | 0.362104 | 0.223456 | | | GRCh38.p7 | 7:95467936 | CACATACATTTTTTT[C/T]TGAGGGAAGAAGAGA | 51666 |
rs2188808 | snp | C/T | 0.45762 | 0.139261 | intron-variant | ASB4 | GRCh38.p7 | 7:95525812 | AAAGATGGTCTTTCA[C/T]GAAGCCATCTGTGTT | 51666 |
rs2240003 | snp | A/G | 0.356169 | 0.226336 | intron-variant | ASB4 | GRCh38.p7 | 7:95535962 | TTCCCAGCTGCCTGG[A/G]AAACTCTTCCAGCTC | 51666 |
rs2301681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95495658 | TTTTTTTTTGGCCAC[A/G]TTTATAAAAGTGGGG | 51666 |
rs2375018 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513254 | tttgttttttgtttg[G/T]ttttttttttttttt | 51666 |
rs2375019 | snp | A/G | 0.281313 | 0.248031 | intron-variant | ASB4 | GRCh38.p7 | 7:95532698 | GAGAAGAGAGGCAGG[A/G]AGACTTACCTTGAAT | 51666 |
rs3045925 | in-del | -/GT | 0 | 0 | | | GRCh38.p7 | 7:95467558 | tgtgtgtgtgtgtgt[-/GT]atgtatgtgtTTATA | 51666 |
rs3046862 | in-del | -/TGTGTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513322 | gtgtgtgtgtgtgtg[-/TGTGTG]tgtgttcagagacag | 51666 |
rs3046863 | in-del | -/GTGTGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513332 | tgtgtgtgtgtgtgt[-/GTGTGT]tcagagacagggaat | 51666 |
rs3046864 | in-del | -/ATA | 0.367495 | 0.220669 | intron-variant | ASB4 | GRCh38.p7 | 7:95522405 | gggcttaagcaaata[-/ATA]tttcattatatcatt | 51666 |
rs3223150 | microsatellite | (CA)17/18/19/20/21/22/23/24 | 0.724772 | 0.127505 | intron-variant | ASB4 | GRCh38.p7 | 7:95493363 | TCCAACCTNGCTATA[(CA)17/18/19/20/21/22/23/24]TTTCATCTCTTTTNT | 51666 |
rs3757702 | snp | A/C | 0.467744 | 0.122832 | intron-variant | ASB4 | GRCh38.p7 | 7:95535659 | CAAGATGGCCAGAAT[A/C]TCCTTCAGGAGATAG | 51666 |
rs3757703 | snp | C/T | 0.468047 | 0.122292 | intron-variant | ASB4 | GRCh38.p7 | 7:95535595 | ATGGATGTTTATACA[C/T]TTAACCAACTTTTGG | 51666 |
rs3757704 | snp | A/C | 0.0652144 | 0.168387 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484108 | ACTCCTAAGTTTAAG[A/C]GAACCTCCTGCCTCA | 51666 |
rs3757705 | snp | C/T | 0.498632 | 0.0261223 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483665 | TGGGAATCCCTAGAT[C/T]GCCTCCATTTCCCAT | 51666 |
rs3779488 | snp | A/C | 0.152667 | 0.230274 | intron-variant | ASB4 | GRCh38.p7 | 7:95513569 | TCACATGTAAATCAG[A/C]AAACTTTGAGTTAAA | 51666 |
rs3779489 | snp | A/T | 0.153332 | 0.230554 | intron-variant | ASB4 | GRCh38.p7 | 7:95511264 | GCGTTCACTTCTTGG[A/T]GGCTCTCGGTAGGGG | 51666 |
rs3779490 | snp | A/G | 0.429388 | 0.174127 | intron-variant | ASB4 | GRCh38.p7 | 7:95491412 | TGAGGGAGAACCGGG[A/G]AACCAAGCCCATGGG | 51666 |
rs3779491 | snp | C/G | 0.325563 | 0.238307 | intron-variant | ASB4 | GRCh38.p7 | 7:95491324 | GCTACCCCATGTCTA[C/G]AGTCTGTGTGCAGTG | 51666 |
rs3801909 | snp | A/C | 0.477515 | 0.103619 | intron-variant | ASB4 | GRCh38.p7 | 7:95532725 | ATTAATACACAATCT[A/C]TTAAAAAAGAGATTC | 51666 |
rs3801912 | snp | A/G | 0.316485 | 0.240998 | intron-variant | ASB4 | GRCh38.p7 | 7:95532341 | ATTCTTTTTTCCCCC[A/G]CTTATGTAATTTACA | 51666 |
rs3801913 | snp | C/T | 0.139564 | 0.224285 | intron-variant | ASB4 | GRCh38.p7 | 7:95526026 | GCTTTAAAAAAAATC[C/T]GTTTACCATGTATTG | 51666 |
rs3801915 | snp | C/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95525704 | GAACGAATGAGAATG[C/T]CTTCCCAGAAGCCAT | 51666 |
rs3801916 | snp | A/G | 0.367297 | 0.220775 | intron-variant | ASB4 | GRCh38.p7 | 7:95491707 | GATGAGGCTGTGCCT[A/G]TTCACAATCTTCTGC | 51666 |
rs3801917 | snp | A/G | 0.368324 | 0.220226 | intron-variant | ASB4 | GRCh38.p7 | 7:95490835 | ATATGCAGACTAATC[A/G]TGTGTGTGTGCACGC | 51666 |
rs3801918 | snp | A/G | 0.286042 | 0.247388 | intron-variant | ASB4 | GRCh38.p7 | 7:95490343 | AAAAGTTTGAACATC[A/G]AAGAAAGGAAAAGAA | 51666 |
rs3801919 | snp | A/G | 0.250168 | 0.25 | intron-variant | ASB4 | GRCh38.p7 | 7:95489698 | TGTTTTCTTTATATC[A/G]TTTTTATTTTAAAGT | 51666 |
rs3801920 | snp | C/T | 0.302686 | 0.244385 | intron-variant | ASB4 | GRCh38.p7 | 7:95489516 | ACATGATTTCATCTG[C/T]AGATTTTATTATGAA | 51666 |
rs3801926 | snp | A/T | 0.283684 | 0.24772 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470659 | AGCTGTGGTGTCAGA[A/T]CCTTTCTCATTTCCT | 51666 |
rs3801927 | snp | A/G | 0.284733 | 0.247575 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470770 | ATAGGACTTTTCAAG[A/G]CACTGTCCCATCCAT | 51666 |
rs3823954 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95488885 | TTTTGTGCATTGTCT[G/T]TCTTATTAAGCCAAA | 51666 |
rs3834352 | in-del | -/TCGGAGAACATAAA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535422 | TTTTCCCATGAAACT[-/TCGGAGAACATAAA]TCAACCTTTCTGAGG | 51666 |
rs3834353 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95532046 | TTCCTTTGGAGGGGG[-/G]CCAGCTCTCCTACAC | 51666 |
rs3837137 | in-del | -/GA | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95491243 | GAAAAGAAAAATAGA[-/GA]TTATTTCCCCTGTGT | 51666 |
rs4517046 | snp | C/T | 0.232651 | 0.249397 | intron-variant | ASB4 | GRCh38.p7 | 7:95534965 | TGTGCTGCCAGCTGG[C/T]TTCATCTTACCAGCT | 51666 |
rs4727314 | snp | A/G | 0.23846 | 0.249734 | | | GRCh38.p7 | 7:95466518 | TTATGGAATCCAAAA[A/G]CAACAGTGAAATATG | 51666 |
rs4729192 | snp | A/G | 0.359998 | 0.2245 | intron-variant | ASB4 | GRCh38.p7 | 7:95500522 | CTGCTGTGAGCTATT[A/G]TTGGACCACTGCACA | 51666 |
rs4729193 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95526385 | CTATAAAACTTCGCT[C/G]CAGTTGCACCCTGCC | 51666 |
rs5885914 | in-del | -/TG | 0.484632 | 0.086302 | | | GRCh38.p7 | 7:95467535 | GAAACATTGTAAAAT[-/TG]TGTGTGTGTGTGTGT | 51666 |
rs5885915 | in-del | -/G | 0.38934 | 0.207568 | | | GRCh38.p7 | 7:95468144 | TTATTAAATTGGGTT[-/G]GGGGGGGCCCCATTC | 51666 |
rs5885916 | in-del | -/T | 0.34989 | 0.229177 | | | GRCh38.p7 | 7:95477921 | TGCAATTTTTTTTTT[-/T]CCTGCAATATCCCAT | 51666 |
rs5885917 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514752 | AGAGGGAGCCTTACC[-/C]TGACTACACACGGGA | 51666 |
rs6465466 | snp | A/C | 0.372189 | 0.218105 | intron-variant | ASB4 | GRCh38.p7 | 7:95502275 | TAAAATGACAATTAG[A/C]TATTTTGTTGTTGTT | 51666 |
rs6465467 | snp | C/T | 0.499354 | 0.0179596 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537892 | ACTTTACAAACACTG[C/T]CATTAATCCTAGAAT | 51666 |
rs6465468 | snp | G/T | 0.266819 | 0.249434 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540202 | GAACTTTTATTTAGA[G/T]AACTTAAATAAAGCT | 51666 |
rs6946568 | snp | A/G | 0.375996 | 0.215928 | intron-variant | ASB4 | GRCh38.p7 | 7:95534206 | AAAAATTAGTCAGGA[A/G]TTGTGGCATGATTTG | 51666 |
rs6950550 | snp | C/G | 0.499017 | 0.0221427 | | | GRCh38.p7 | 7:95480115 | AGACTTTTCTTACTT[C/G]TTGGTCCACAGGAGC | 51666 |
rs6952627 | snp | C/G | 0.436692 | 0.166271 | intron-variant | ASB4 | GRCh38.p7 | 7:95498222 | acacctataatatca[C/G]tattttgggaggcca | 51666 |
rs6958904 | snp | C/T | 0.418007 | 0.185132 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484865 | AAGCTGAAAGAATAA[C/T]GTAATGGATACCAAT | 51666 |
rs6958950 | snp | C/G | 0.493837 | 0.055168 | intron-variant | ASB4 | GRCh38.p7 | 7:95523959 | tcactctgcaaccaa[C/G]aaattggctaaaatt | 51666 |
rs6959029 | snp | A/G | 0.491936 | 0.0629843 | intron-variant | ASB4 | GRCh38.p7 | 7:95524240 | gggcaatgcccatct[A/G]cagttgaatggataa | 51666 |
rs6959064 | snp | C/T | 0.103082 | 0.202275 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484961 | ttacacaCACatata[C/T]atatgtgtgtatata | 51666 |
rs6959226 | snp | C/T | 0.123798 | 0.215808 | intron-variant | ASB4 | GRCh38.p7 | 7:95515159 | TTTTTCTTTCTTTCT[C/T]TCTCTTTCTCTTTCT | 51666 |
rs6960785 | snp | C/T | 0.0825414 | 0.185628 | | | GRCh38.p7 | 7:95481959 | CAGTGTGAAACATGA[C/T]CACTGTGTAATTTGA | 51666 |
rs6969315 | snp | C/T | 0.153 | 0.230415 | intron-variant | ASB4 | GRCh38.p7 | 7:95518736 | ATTCCACTGCAGGAA[C/T]GACCAATGAGATTTT | 51666 |
rs6973126 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | ASB4 | GRCh38.p7 | 7:95501905 | TTAAAGATCCACTTA[C/T]TCTTTCAAGCCATGT | 51666 |
rs6973299 | snp | C/G | 0.439085 | 0.163545 | intron-variant | ASB4 | GRCh38.p7 | 7:95501998 | TCAGAAGGGCAAACA[C/G]CATAAAATTAAAAGG | 51666 |
rs6975716 | snp | G/T | 0.31721 | 0.240796 | intron-variant | ASB4 | GRCh38.p7 | 7:95520163 | AATAATTTGAATTCT[G/T]AATTTTGAAAGTGTC | 51666 |
rs6976899 | snp | A/G | 0.484209 | 0.0874434 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484800 | TAAGAAAAATTAAGT[A/G]TATACTTTTCTCTCC | 51666 |
rs6979120 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | ASB4 | GRCh38.p7 | 7:95524150 | tagagcccagagaaa[C/T]ccctgcacgtgagca | 51666 |
rs7455777 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513243 | TCAGGGttttttttg[G/T]tttttgtttgttttt | 51666 |
rs7457858 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513242 | GTCAGGGtttttttt[G/T]ttttttgtttgtttt | 51666 |
rs7779320 | snp | A/C | 0.206336 | 0.246157 | intron-variant | ASB4 | GRCh38.p7 | 7:95537254 | ACTTCCATTAAATAT[A/C]TGAATATATGCATCA | 51666 |
rs7784619 | snp | A/G | 0.498794 | 0.0245311 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538231 | ACTGTCACTAGTTTT[A/G]CAAACTCCTACTCCC | 51666 |
rs7791764 | snp | C/T | 0.0562307 | 0.157967 | | | GRCh38.p7 | 7:95463695 | tgcttcctgcgcagc[C/T]tgtggaactgtgagc | 51666 |
rs7795412 | snp | A/G | 0.293294 | 0.246223 | intron-variant | ASB4 | GRCh38.p7 | 7:95529806 | ttttatttttataat[A/G]gactctgaggtgggc | 51666 |
rs7798235 | snp | C/T | 0.4776 | 0.103433 | intron-variant | ASB4 | GRCh38.p7 | 7:95533601 | TGAATGCTTTCTTCA[C/T]TTGGTATCTTTCACT | 51666 |
rs7806277 | snp | C/G | 0.326506 | 0.238006 | intron-variant | ASB4 | GRCh38.p7 | 7:95502391 | ATAGGTACCAGCCTG[C/G]GGGGGGGGGGCAAAT | 51666 |
rs9886182 | snp | A/G | 0.427423 | 0.176128 | intron-variant | ASB4 | GRCh38.p7 | 7:95500011 | cccaagtagctggga[A/G]CATCCTCATTTTTAA | 51666 |
rs9886222 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95501444 | AATCCGAAATAGATA[G/T]GCCTGCTGGACAGAC | 51666 |
rs10225152 | snp | A/G | 0.207864 | 0.246424 | intron-variant | ASB4 | GRCh38.p7 | 7:95512968 | TAAGAACTTTGAGAT[A/G]AGGAGATTATCTTGG | 51666 |
rs10225626 | snp | A/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95513276 | ttttttttttttttA[A/G]AAATCGAGCCAATAG | 51666 |
rs10225645 | snp | A/G | 0.499879 | 0.0077866 | | | GRCh38.p7 | 7:95483239 | CATGAGGTCTCGTAA[A/G]CTGCACTCTTACTGC | 51666 |
rs10227770 | snp | A/G/T | 0.0209737 | 0.100468 | | | GRCh38.p7 | 7:95465973 | caaaaagacaaCTGA[A/G/T]TGCAAGTCTTCCCAA | 51666 |
rs10229266 | snp | C/T | 0.0154538 | 0.0865337 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474887 | TGGTTTTACCCCAAA[C/T]AGGCATGTAGTTAAG | 51666 |
rs10229573 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASB4 | GRCh38.p7 | 7:95535360 | GAGGCATGCCTCTCT[C/T]CTAATGCCTCACCTA | 51666 |
rs10233276 | snp | A/C | 0.0154538 | 0.0865337 | | | GRCh38.p7 | 7:95477818 | GTGTTGTTTCTCTTT[A/C]GGTATACTATTTTTC | 51666 |
rs10234015 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASB4 | GRCh38.p7 | 7:95502493 | TCTAGGCAGGAGACC[A/G]TTTTACCCAGGGCTG | 51666 |
rs10236739 | snp | A/C | 0.0535932 | 0.154675 | | | GRCh38.p7 | 7:95461236 | aaagccacagacact[A/C]aatgccagcccatga | 51666 |
rs10240833 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASB4 | GRCh38.p7 | 7:95492248 | CAAGGATGACTGACT[C/T]ACATAATACACGAAC | 51666 |
rs10241004 | snp | G/T | 0.499137 | 0.0207489 | | | GRCh38.p7 | 7:95483252 | AAGCTGCACTCTTAC[G/T]GCTGACTGCTATTCA | 51666 |
rs10244306 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | ASB4 | GRCh38.p7 | 7:95522611 | ggaaGTGTCTGGAAG[C/G]GTTGGGAAGCACTTA | 51666 |
rs10246739 | snp | A/G | 0.0244538 | 0.107838 | | | GRCh38.p7 | 7:95475549 | ccaccacacctggct[A/G]agttttgtattttta | 51666 |
rs10247338 | snp | C/T | 0.230017 | 0.2492 | intron-variant | ASB4 | GRCh38.p7 | 7:95519748 | CTAAGAAAAGTGTAA[C/T]TTTTTAAGGTGATGT | 51666 |
rs10248295 | snp | G/T | 0.437401 | 0.165472 | intron-variant | ASB4 | GRCh38.p7 | 7:95499364 | gagaaaccagtaaag[G/T]agagtaagatatact | 51666 |
rs10248407 | snp | A/G | 0.3742 | 0.216966 | intron-variant | ASB4 | GRCh38.p7 | 7:95499441 | acaaagaaagaggta[A/G]taggttccagaagca | 51666 |
rs10248757 | snp | C/T | 0.427879 | 0.175668 | intron-variant | ASB4 | GRCh38.p7 | 7:95493891 | ATAGTATTTGATTGA[C/T]GGATGTATCATAATT | 51666 |
rs10251591 | snp | C/T | 0.230017 | 0.2492 | intron-variant | ASB4 | GRCh38.p7 | 7:95520776 | TACAGATGCTTTCTG[C/T]AGGTAGGTCTGTTTC | 51666 |
rs10252444 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515485 | cagtgatgtgatctc[G/T]gctcactgcaacctc | 51666 |
rs10252655 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515679 | cttggcctcccaaag[G/T]gctgggactacaggc | 51666 |
rs10253948 | snp | A/G | 0.209084 | 0.246629 | intron-variant | ASB4 | GRCh38.p7 | 7:95512753 | ATAGCTAGAAGGGGA[A/G]CTCACATTTGGTGCA | 51666 |
rs10264477 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | ASB4 | GRCh38.p7 | 7:95494161 | CTAGTGTTTTTCACT[G/T]AAATGAGAGAAATTT | 51666 |
rs10268588 | snp | C/T | 0.437683 | 0.165152 | intron-variant | ASB4 | GRCh38.p7 | 7:95495069 | TTGTGTATGTATTTG[C/T]CTTACTTTTGACATT | 51666 |
rs10272732 | snp | C/T | 0.0154538 | 0.0865337 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474981 | CAGGAGATACTTTTG[C/T]AATATGATCCTTAGG | 51666 |
rs10275596 | snp | A/G | 0.493658 | 0.0559517 | intron-variant | ASB4 | GRCh38.p7 | 7:95510858 | AAATTGAAGGATGAA[A/G]TTTCCTTAGGCCTGT | 51666 |
rs10278137 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ASB4 | GRCh38.p7 | 7:95516495 | GATAAATAAACATGG[A/G]TTCAATGAAAAAAAT | 51666 |
rs10278417 | snp | A/G | 0.499703 | 0.0121769 | intron-variant | ASB4 | GRCh38.p7 | 7:95494158 | TCTCTAGTGTTTTTC[A/G]CTTAAATGAGAGAAA | 51666 |
rs10279960 | snp | C/G | 0.493154 | 0.0581045 | intron-variant | ASB4 | GRCh38.p7 | 7:95512247 | GGAGTAAGACGGACT[C/G]GGTTCAGACCTTGAC | 51666 |
rs10280214 | snp | C/T | 0.0244538 | 0.107838 | | | GRCh38.p7 | 7:95482329 | GGGAAAAATTATAGC[C/T]ATCTCTTTAGGCTAA | 51666 |
rs10480616 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | ASB4 | GRCh38.p7 | 7:95486661 | AAAGCGGTGCCACAG[G/T]CACCTTCATGGTCTT | 51666 |
rs10487135 | snp | A/G | 0.158302 | 0.232576 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528623 | GAATAGTGTTAGACA[A/G]GCATACATTTGCCAT | 51666 |
rs10643021 | in-del | -/AAAG | 0.398534 | 0.201091 | | | GRCh38.p7 | 7:95467044 | CTAGAACCACAAAAT[-/AAAG]AATGATTTTTTTCTG | 51666 |
rs10675614 | in-del | -/TATG | 0.447291 | 0.153545 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472232 | ATTCTTTCCCCAAAA[-/TATG]ATGTGTCCAAAATTG | 51666 |
rs10953148 | snp | G/T | 0.498547 | 0.0269177 | | | GRCh38.p7 | 7:95459702 | ACCAAAGAACAGGCA[G/T]ATATGATTAAAGGGT | 51666 |
rs10953149 | snp | A/T | 0.482459 | 0.0919928 | | | GRCh38.p7 | 7:95459797 | TATTTTCTGTCGGTG[A/T]CTACTGGTGTTTCTA | 51666 |
rs10953150 | snp | A/T | 0.499137 | 0.0207489 | | | GRCh38.p7 | 7:95462479 | TCCTTTAAAAAAAAA[A/T]TTACCTCTGTGACAG | 51666 |
rs10953151 | snp | C/T | 0.482534 | 0.0918038 | | | GRCh38.p7 | 7:95462586 | GTCTGTCATCTAGAA[C/T]GAGAAGATAATGAAT | 51666 |
rs10953152 | snp | A/G | 0.498589 | 0.02652 | | | GRCh38.p7 | 7:95462648 | GGCTTACATAACATG[A/G]AACTCATTTAACAAA | 51666 |
rs11285695 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502392 | TAGGTACCAGCCTGC[-/G]GGGGGGGGGCAAATT | 51666 |
rs11359538 | in-del | -/C | 0.408359 | 0.193449 | intron-variant | ASB4 | GRCh38.p7 | 7:95505687 | TTCCTCTATCCGTGT[-/C]CCCCCCCCCCCAAAT | 51666 |
rs11431388 | in-del | -/A | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484027 | AAAAAAAAAAAAAAA[-/A]TTGTCAGGCATAGTG | 51666 |
rs11479848 | in-del | -/A | 0.484279 | 0.0872533 | intron-variant | ASB4 | GRCh38.p7 | 7:95534342 | ACGTAAAACTCCATT[-/A]AAAAAAAAAAAGATG | 51666 |
rs11764055 | snp | C/T | 0.274661 | 0.248781 | intron-variant | ASB4 | GRCh38.p7 | 7:95491900 | AAAGCAGCAGACTTT[C/T]CTGATATGCTCAGGG | 51666 |
rs11768402 | snp | C/T | 0.25214 | 0.249991 | intron-variant | ASB4 | GRCh38.p7 | 7:95531541 | GAGAAGTGGTTAGCA[C/T]GGTGCCATGGGCATG | 51666 |
rs11772047 | snp | G/T | 0.375399 | 0.216275 | intron-variant | ASB4 | GRCh38.p7 | 7:95507154 | tttgtttgtttgttt[G/T]tttgctgcagggtat | 51666 |
rs11971756 | snp | C/G | 0.499396 | 0.0173617 | intron-variant | ASB4 | GRCh38.p7 | 7:95488675 | TTTTGGACCTTGGAC[C/G]CTGTTGAACTGCTAC | 51666 |
rs11972076 | snp | A/C | 0.0349115 | 0.127424 | | | GRCh38.p7 | 7:95476871 | CATTGTAGCAAAAAC[A/C]AACAATAAAGGGACA | 51666 |
rs11973603 | snp | G/T | 0.230017 | 0.2492 | intron-variant | ASB4 | GRCh38.p7 | 7:95517446 | ATAGTAGTTTTGATT[G/T]CTCCAGGAAGTTATG | 51666 |
rs11974265 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | ASB4 | GRCh38.p7 | 7:95537124 | GGTATCAGGCACAGG[A/G]TGCAAAGTTCACTGG | 51666 |
rs11975318 | snp | G/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95488477 | GCTAGTAGATCTAAG[G/T]GGTTATATCAATTTC | 51666 |
rs11975820 | snp | A/G | 0.49089 | 0.0668743 | | | GRCh38.p7 | 7:95463176 | CAGTAGGGCCCACAA[A/G]TGCACACCACCACAC | 51666 |
rs11977715 | snp | A/G | 0.207559 | 0.246371 | intron-variant | ASB4 | GRCh38.p7 | 7:95488391 | TTTCACATGCTTCCA[A/G]CCTTATCATCGATCC | 51666 |
rs11978540 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASB4 | GRCh38.p7 | 7:95526218 | caatgaggaaggggt[C/T]cccagtgggagagag | 51666 |
rs11978838 | snp | A/G | 0.0352966 | 0.128072 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484000 | ttaaaatcttcaaaa[A/G]ttgtaaaatgtttaa | 51666 |
rs11982442 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493158 | AATATATTAGAATTT[A/C]ATTCTATTAGCTGAA | 51666 |
rs11982574 | snp | C/T | 0.310386 | 0.242597 | | | GRCh38.p7 | 7:95477117 | TGGATTTTTTTTTTT[C/T]CCCCAGGATACTGCA | 51666 |
rs12154697 | snp | A/G | 0.303438 | 0.244222 | intron-variant | ASB4 | GRCh38.p7 | 7:95510579 | TTTTTTTCTCCAAAC[A/G]CTAATTGTTTTGGTC | 51666 |
rs12533957 | snp | C/T | 0.386884 | 0.209196 | intron-variant | ASB4 | GRCh38.p7 | 7:95497922 | acaaaattgatctac[C/T]ccccagtagagggac | 51666 |
rs12534203 | snp | C/G | 0.499218 | 0.0197529 | | | GRCh38.p7 | 7:95462732 | AAATGTATGCATCAA[C/G]TAGTATTAGCATTTG | 51666 |
rs12535086 | snp | A/T | 0.029116 | 0.117091 | intron-variant | ASB4 | GRCh38.p7 | 7:95511671 | CCGTCTCAAAAAAAA[A/T]AAATAAATAAATAAA | 51666 |
rs12538293 | snp | A/C | 0.28578 | 0.247426 | intron-variant | ASB4 | GRCh38.p7 | 7:95496477 | GAGTTATGAATGAGG[A/C]TGTCAGAAGTGAATT | 51666 |
rs12538469 | snp | G/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95504262 | TTCAAATGTTCCTTA[G/T]CAGAAAGTGACATGG | 51666 |
rs12539110 | snp | A/T | 0.386884 | 0.209196 | intron-variant | ASB4 | GRCh38.p7 | 7:95497766 | ttcagaatgtcatat[A/T]cattaaaatataaaa | 51666 |
rs12539224 | snp | G/T | 0.410061 | 0.192043 | intron-variant | ASB4 | GRCh38.p7 | 7:95526466 | TTTTCATACATACTT[G/T]CTCTAATAAATCTGC | 51666 |
rs12539808 | snp | A/T | 0.35894 | 0.225016 | intron-variant | ASB4 | GRCh38.p7 | 7:95498606 | ctagtcatttatcag[A/T]tacatagtttgcacg | 51666 |
rs12670004 | snp | G/T | 0.25912 | 0.249834 | intron-variant | ASB4 | GRCh38.p7 | 7:95529706 | TAGGGAACTACAAAT[G/T]ATTAAGATGAGGAAT | 51666 |
rs13222447 | snp | A/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95513291 | GAAATCGAGCCAATA[A/G]AAtgtgtgtgtgtgt | 51666 |
rs13222459 | snp | A/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95513336 | gtgtgtgtgtgttca[A/G]agacagggaatggaa | 51666 |
rs13222727 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500596 | aaaaaaaaaaaaaaa[A/G]GCCATGATCTTTTCA | 51666 |
rs13227052 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522968 | CCAGAAACAATGTAC[C/T]CTGCCCACTTAGAAT | 51666 |
rs13227440 | snp | A/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95523219 | AACTTCTGAAAGGAG[A/T]AGGACATTCTGGTAC | 51666 |
rs13229811 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515252 | TTCTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTC | 51666 |
rs13229921 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515320 | CTTTCTTTCTTTCTT[C/T]CTTCCTTCCTTCCTT | 51666 |
rs13229930 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515328 | ctttcttccttcctt[C/T]cttcctttctttctt | 51666 |
rs13238692 | snp | A/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95505078 | ttctgctctcgtcac[A/G]gtctcttcagccctg | 51666 |
rs13238789 | snp | C/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95505113 | ggaggtcctaactgg[C/G]acaaagagaagagaa | 51666 |
rs13238790 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505115 | aggtcctaactggca[C/G]aaagagaagagaaaa | 51666 |
rs13239766 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522966 | CCCCAGAAACAATGT[A/C]CTCTGCCCACTTAGA | 51666 |
rs13244083 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515147 | TCCAAGCAATTGTTt[G/T]tctttctttctttct | 51666 |
rs13244198 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515264 | ttccttctttctttc[C/T]ttctctttctttctt | 51666 |
rs13244302 | snp | C/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95515336 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 51666 |
rs13244304 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ASB4 | GRCh38.p7 | 7:95515344 | cttcctttctttctt[C/T]ctttctttttctttc | 51666 |
rs13246356 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530052 | gaaacaaacaaaaca[A/C]caaccaaataaatat | 51666 |
rs17166907 | snp | C/G | 0.0302959 | 0.11929 | intron-variant | ASB4 | GRCh38.p7 | 7:95491320 | CTGTCACTGCACACA[C/G]ACTCTAGACATGGGG | 51666 |
rs17703967 | snp | C/T | 0.314301 | 0.241589 | intron-variant | ASB4 | GRCh38.p7 | 7:95495591 | TGCTATTTAACAAAA[C/T]GCTTGCAGACCCATT | 51666 |
rs17703998 | snp | A/G | 0.226484 | 0.248892 | intron-variant | ASB4 | GRCh38.p7 | 7:95503085 | GACTATGCATATCAA[A/G]ATAATATTTAAAATA | 51666 |
rs17704028 | snp | C/T | 0.178144 | 0.239451 | intron-variant | ASB4 | GRCh38.p7 | 7:95510719 | CACCTGTTAGCATTA[C/T]AGGTTTCCTTCTCTG | 51666 |
rs17704073 | snp | G/T | 0.128632 | 0.218563 | intron-variant | ASB4 | GRCh38.p7 | 7:95516116 | ACTTTATCCAAACTT[G/T]TATCTTCTAAAAAAA | 51666 |
rs17704092 | snp | C/T | 0.128632 | 0.218563 | intron-variant | ASB4 | GRCh38.p7 | 7:95516695 | AGAGCAGACCAAGTG[C/T]CAAAAAGTTTGGTTT | 51666 |
rs17704140 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ASB4 | GRCh38.p7 | 7:95533175 | TAAACTCTGTCTGCC[A/G]GGGAGAGGCCTGCAA | 51666 |
rs17717858 | snp | A/G | 0.360421 | 0.224293 | intron-variant | ASB4 | GRCh38.p7 | 7:95495207 | TTGCATAAATCAACA[A/G]GCAGGCAAATAAAAT | 51666 |
rs17717907 | snp | A/G | 0.359787 | 0.224604 | intron-variant | ASB4 | GRCh38.p7 | 7:95502655 | CACATGACCTGCAGT[A/G]CACTAGAAATTAGAG | 51666 |
rs17717920 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | ASB4 | GRCh38.p7 | 7:95507669 | TGTTAAAAATTTATT[C/G]AATGTTCAATTGACA | 51666 |
rs17774689 | snp | A/G | 0.144296 | 0.226554 | intron-variant | ASB4 | GRCh38.p7 | 7:95512424 | TGTGAAAGTATCTTT[A/G]TGTTGTCTAGAAATG | 51666 |
rs17774768 | snp | A/G | 0.159622 | 0.233092 | intron-variant | ASB4 | GRCh38.p7 | 7:95529398 | GAATTCACAGCTTAA[A/G]TTCTACGTCTTACCT | 51666 |
rs28414348 | snp | C/T | 0.175897 | 0.238765 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538122 | GTGCCTTATCAGTAA[C/T]ATGTTTACATTCTCA | 51666 |
rs28430840 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538910 | GTGACAGTGGGCTAC[A/G]AAAAGTAAATAGAGA | 51666 |
rs28444509 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505804 | TTTGTTATCTCTGTA[A/G]AAAACTGTCTTATTT | 51666 |
rs28469352 | snp | C/G | | | | | GRCh38.p7 | 7:95465549 | CTGCTGCCCAGGCTG[C/G]AGTGCGGTGGCATGG | 51666 |
rs28571007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95498199 | AATTAGGCTGGGCAC[A/G]GTGGCTCACACCTAT | 51666 |
rs28618177 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | ASB4 | GRCh38.p7 | 7:95491933 | GAATTATTCAAAAAT[A/C]CCTAGCCCCACATTA | 51666 |
rs28721388 | snp | G/T | 0.416871 | 0.186156 | intron-variant | ASB4 | GRCh38.p7 | 7:95488251 | GAGGCTGAGACAGGA[G/T]AATGGTGTGAACCCG | 51666 |
rs28889731 | snp | A/T | 0.493154 | 0.0581045 | intron-variant | ASB4 | GRCh38.p7 | 7:95506657 | TTTTTTATGTGAATT[A/T]TTATCTTCCTCTCTG | 51666 |
rs34107708 | in-del | -/T | | | | | GRCh38.p7 | 7:95464727 | TACAGTTAACCTTTT[-/T]CCCCATGAGACACAT | 51666 |
rs34109833 | in-del | -/AT | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484956 | TCTATTTACACACAC[-/AT]ATATATATGTGTGTA | 51666 |
rs34122730 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506935 | AATTATCTTGTATTG[G/T]CTCGTCTCTCCTATT | 51666 |
rs34231561 | in-del | -/T | 0.472803 | 0.113397 | | | GRCh38.p7 | 7:95477736 | CCCTTAACAAGAACC[-/T]TTTTTTTTTTTTTTG | 51666 |
rs34260018 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529156 | TAAATGACAAGGTAG[-/T]AAGAATAATGAGTGC | 51666 |
rs34269533 | in-del | -/GT | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95493391 | TGTGTGTGTGTGTGT[-/GT]ATGTGTGTGTGTGTG | 51666 |
rs34276025 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504676 | TATTACTATAAAAAA[-/A]TTGAAACCCAAAATC | 51666 |
rs34361311 | in-del | -/T | 0.498415 | 0.0281103 | | | GRCh38.p7 | 7:95462391 | TATTTAAAAAAGTTC[-/T]TTTTTTTTTCTAAGA | 51666 |
rs34375136 | in-del | -/A | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468864 | TTTGTGACAGTTCAA[-/A]TTTAGTCTTTTGTTG | 51666 |
rs34493569 | in-del | -/C | | | | | GRCh38.p7 | 7:95466735 | TGGACTAACAATTCC[-/C]ACATGGCTGGGGAGG | 51666 |
rs34504415 | in-del | -/C | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474282 | CTATTTATATTTTCC[-/C]TTTTGGGGAGGTCAA | 51666 |
rs34510999 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530525 | GATGGGGAGGTGGGG[-/G]AGAGCATTCCAGGCC | 51666 |
rs34678005 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524072 | ACAACTGCTTATTTG[-/G]ACAGTACTTAATGAA | 51666 |
rs34680829 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510533 | TATGTTAAATATCCC[-/C]TGTCACTAAACTTAG | 51666 |
rs34695168 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525903 | TCTTGGGTACCTTCC[-/C]TTGGGGACTGAGTTT | 51666 |
rs34758617 | in-del | -/T | | | | | GRCh38.p7 | 7:95462711 | AAAAAATACTAATTT[-/T]AGCAAAAATGTATGC | 51666 |
rs34852544 | in-del | -/G | | | | | GRCh38.p7 | 7:95464500 | AATGCTTAAACATCG[-/G]CCCATATTTTGTAAT | 51666 |
rs34888731 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534014 | AATAACTCCATCTTA[A/G]CTTTCTAATGGGGAG | 51666 |
rs34898299 | in-del | -/AAAG | | | | | GRCh38.p7 | 7:95467045 | TAGAACCACAAAATA[-/AAAG]ATGATTTTTTTCTGT | 51666 |
rs34952249 | in-del | -/AT | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485064 | TATATATGTATATAT[-/AT]GTATATACACATACA | 51666 |
rs34984005 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514509 | TGGACAGACAACCCC[-/C]TCCAAGAGTTAGAGG | 51666 |
rs35047380 | snp | C/G | 0.0206382 | 0.0994645 | missense | ASB4 | GRCh38.p7 | 7:95486020 | GGAAATTTCTCTTAA[C/G]TAACTTGGCAGCTCC | 51666 |
rs35065632 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505006 | TTTCAAGTTGATAGT[-/G]CTATTTAGTGGTGAA | 51666 |
rs35072651 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532597 | GATCATTAAGTACCT[-/C]TTCTGAACACATATA | 51666 |
rs35075679 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487384 | TAATTTTGTTCAGTG[-/C]ATAGAATGTCTGAAT | 51666 |
rs35122394 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | ASB4 | GRCh38.p7 | 7:95518064 | CTACTTCCCCTAAAA[A/G]GATAGAGAGAAGGTA | 51666 |
rs35236189 | in-del | -/A | 0.477175 | 0.104362 | intron-variant | ASB4 | GRCh38.p7 | 7:95521687 | TCAGCAGTTGAAATT[-/A]AAAAAAAAAAAACAG | 51666 |
rs35294277 | in-del | -/C | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470924 | CTCCGGGTGGTTCCC[-/C]TGTTTACAAAGTAAG | 51666 |
rs35308529 | in-del | -/C | | | | | GRCh38.p7 | 7:95475158 | TGTTGTAACAAGCCC[-/C]ACCAGAGGACTCTGA | 51666 |
rs35411461 | in-del | -/AGAA | | | | | GRCh38.p7 | 7:95467046 | AGAACCACAAAATAA[-/AGAA]TGATTTTTTTCTGTG | 51666 |
rs35506436 | in-del | -/T | 0.0626345 | 0.165512 | intron-variant | ASB4 | GRCh38.p7 | 7:95495739 | AAACTTTCCTTTTCC[-/T]TTTTTTTTTTTTTTT | 51666 |
rs35543427 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531818 | CATAAGCATCTCCCC[-/C]TGCTGGCTTTTCTTG | 51666 |
rs35668233 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492280 | GGATAGAGTCTTTAG[-/G]TGCTACCTGGAAGTT | 51666 |
rs35697414 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493866 | AACTGCCCCTTTTTT[-/T]AATGGTTGTATAGTA | 51666 |
rs35768280 | in-del | -/G | | | | | GRCh38.p7 | 7:95478331 | AACTGTGCTGGACGG[-/G]CGTGTAAATGCAGGT | 51666 |
rs35768938 | in-del | -/C | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473475 | CAGTGATGAGTTCCC[-/C]AGCGGAGCCTGGCTG | 51666 |
rs35776056 | snp | A/C | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95526757 | ACTAGCATAATAATA[A/C]CAATAATAATAATAA | 51666 |
rs35946956 | in-del | -/A | | | | | GRCh38.p7 | 7:95463991 | TTTTAACTAAAGTGG[-/A]AAAAGATGCCCTAGT | 51666 |
rs35949396 | in-del | -/A | | | | | GRCh38.p7 | 7:95464465 | CTTGAAAACAACAAA[-/A]TGCAAATAGTGCTTG | 51666 |
rs35989056 | in-del | -/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470822 | TAGGGTTTTCTTTTT[-/T]CCCCCCATTAGGAAA | 51666 |
rs36023908 | snp | C/T | 0.155656 | 0.231515 | intron-variant | ASB4 | GRCh38.p7 | 7:95517313 | TGCTGGGACTACAGA[C/T]GTTAGCCACCATGCC | 51666 |
rs36043642 | in-del | -/TT | | | | | GRCh38.p7 | 7:95463059 | TTTTTTTTTTTTTTT[-/TT]AAGAGACAAGGTCTT | 51666 |
rs36045640 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506704 | TTTTTTTTTTTTTTT[-/T]GGTCTTTGATGTTCT | 51666 |
rs36057956 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532598 | ATCATTAAGTACCTT[-/C]TCTGAACACATATAT | 51666 |
rs36097927 | in-del | -/A | 0.493293 | 0.0575177 | intron-variant | ASB4 | GRCh38.p7 | 7:95524499 | GGCTTTACAATAATT[-/A]AAAAAAACTGTACAT | 51666 |
rs36099978 | in-del | -/A | | | | | GRCh38.p7 | 7:95478449 | AAAGATGACGTGAAA[-/A]TGAATAGTCTGTCAA | 51666 |
rs55639050 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95498692 | GAGAAGAAGTATTTA[A/G]TTCTGATAAATTCAA | 51666 |
rs55908284 | snp | A/G | 0.20111 | 0.245173 | | | GRCh38.p7 | 7:95461473 | CCATTTGGAATGAGT[A/G]TATTTACCCAATGCC | 51666 |
rs55939752 | in-del | -/TA | 0.5 | 0 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539086 | TTTTTTTGTTCTTGC[-/TA]TAATCACTTTTAGAT | 51666 |
rs56140670 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95498342 | ATATTGGCTAACATT[C/T]TAAATGTCCCTCTAC | 51666 |
rs57366973 | in-del | -/C | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95502391 | ATAGGTACCAGCCTG[-/C]GGGGGGGGGGCAAAT | 51666 |
rs57750807 | snp | C/G | 0.00835141 | 0.0640778 | | | GRCh38.p7 | 7:95482643 | GTTTCTTTCACAAGG[C/G]AAAGATGATAACCAT | 51666 |
rs58222360 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95495539 | TAGAGACAGTGAGAG[C/T]TTGAGAAAGCCTGTT | 51666 |
rs58483065 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASB4 | GRCh38.p7 | 7:95512396 | TAAGGCTCTTTTCCC[C/T]CATCCCTGGACCTGT | 51666 |
rs58527791 | in-del | -/T | | | | | GRCh38.p7 | 7:95462250 | AATATATATATTTTT[-/T]GGTCCAGGATTCTTT | 51666 |
rs58930216 | snp | A/C | 0.157311 | 0.232183 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528558 | GCCTTGTGTGAACAC[A/C]AGTGCACTGGTGGCT | 51666 |
rs59348835 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95505848 | AATTTTCTACATACT[A/C]ATTGCTATTTAACCT | 51666 |
rs59513981 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95492299 | TACCTGGAAGTTAGG[A/C]GGAGGAAAAAAATTC | 51666 |
rs59576013 | snp | A/T | 0.155656 | 0.231515 | intron-variant | ASB4 | GRCh38.p7 | 7:95523725 | TACAAAATTATTAAT[A/T]GTAGCATTAATTTTA | 51666 |
rs59849439 | snp | A/G | 0.301681 | 0.2446 | | | GRCh38.p7 | 7:95462801 | AAAGACATACCACAA[A/G]CACAAATTGAGCTAT | 51666 |
rs59970043 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ASB4 | GRCh38.p7 | 7:95513029 | TCAGGGACCTTTTTT[A/G]GCTATAGTTAGAGGA | 51666 |
rs60169242 | snp | A/G | 0.029116 | 0.117091 | | | GRCh38.p7 | 7:95461413 | GCCCTATTGGATTTC[A/G]GACTTGCATGGGACC | 51666 |
rs60676979 | in-del | -/C | 0.498547 | 0.0269177 | | | GRCh38.p7 | 7:95463682 | GCCTCTCCAGCCATG[-/C]TTCCTGCGCAGCCTG | 51666 |
rs60923712 | in-del | -/AAAAAA/AAAAAAAA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530120 | AAAAAAAAAAAAAAA[-/AAAAAA/AAAAAAAA]GAGAATGCCAGATTA | 51666 |
rs60991985 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512112 | TGTAACACTTGATCC[-/C]TCCCATGCTGTAGCC | 51666 |
rs61121205 | snp | C/G | 0.467642 | 0.123012 | intron-variant | ASB4 | GRCh38.p7 | 7:95531334 | CAAAAACATCTACCT[C/G]TGTAATACAGCTCAC | 51666 |
rs61250820 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499890 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC | 51666 |
rs61309797 | snp | A/T | 0.077417 | 0.180873 | | | GRCh38.p7 | 7:95462245 | GATATAAATATATAT[A/T]TTTTTGGTCCAGGAT | 51666 |
rs61336573 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493479 | TTCATTCCTGTGGGA[C/T]TAATCACTGTGCACA | 51666 |
rs61530781 | snp | C/G | 0.417034 | 0.18601 | intron-variant | ASB4 | GRCh38.p7 | 7:95488804 | CTATGTAACCAGCAT[C/G]CAGATGAGGAAACAG | 51666 |
rs62467669 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95459821 | GTTTCTAGATTGTGG[C/T]TGATATGGTTTAGCT | 51666 |
rs62467670 | snp | C/G | 0.5 | 0 | | | GRCh38.p7 | 7:95461880 | CATCAACTAAGTGGG[C/G]CTTAAAAGGGGCTTT | 51666 |
rs62467671 | snp | A/C | 0.0252325 | 0.109451 | | | GRCh38.p7 | 7:95462221 | TCCTCCTTTCAAAGT[A/C]TTCTCTGTGATATAA | 51666 |
rs62467672 | snp | A/T | | | | | GRCh38.p7 | 7:95465515 | TAAAAAAAAAAAATT[A/T]CTGAGACAGGGTCTT | 51666 |
rs62467673 | snp | C/G | | | | | GRCh38.p7 | 7:95468155 | GGTTGGGGGGGGCCC[C/G]ATTCAACCTAAATGC | 51666 |
rs62467674 | snp | A/T | 0.02016 | 0.0983543 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484074 | GGCTCATGGCTGTAA[A/T]CCCAGCGCTTTGGAT | 51666 |
rs62467675 | snp | C/T | 0.117886 | 0.21224 | intron-variant | ASB4 | GRCh38.p7 | 7:95490939 | ACTGCATGTAGCCTT[C/T]GGATCATAGACGGCT | 51666 |
rs62467676 | snp | A/C/T | 0.0829401 | 0.188911 | intron-variant | ASB4 | GRCh38.p7 | 7:95490950 | CCTTCGGATCATAGA[A/C/T]GGCTATTTAAAGATT | 51666 |
rs62467677 | snp | C/T | 0.117537 | 0.212022 | intron-variant | ASB4 | GRCh38.p7 | 7:95492454 | AAGACAGATGAAAAC[C/T]GCATTGCGGGTATTC | 51666 |
rs62467678 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ASB4 | GRCh38.p7 | 7:95503741 | AGGACCACAGAAGTC[C/T]GTTAGAGGAAGAACC | 51666 |
rs62467679 | snp | A/G | 0.132066 | 0.220435 | intron-variant | ASB4 | GRCh38.p7 | 7:95505073 | AACTTTTCTGCTCTC[A/G]TCACAGTCTCTTCAG | 51666 |
rs62467680 | snp | A/G | 0.130351 | 0.219509 | intron-variant | ASB4 | GRCh38.p7 | 7:95505683 | CCTTTTCCTCTATCC[A/G]TGTCCCCCCCCCCCC | 51666 |
rs62467681 | snp | C/T | 0.127944 | 0.218179 | intron-variant | ASB4 | GRCh38.p7 | 7:95513927 | AATTCTGCCATCATC[C/T]ACGAAGGATTTCGAT | 51666 |
rs62467682 | snp | A/G | 0.128632 | 0.218563 | intron-variant | ASB4 | GRCh38.p7 | 7:95517369 | GTATTCTAGACACGA[A/G]TCTTTTATCATATAT | 51666 |
rs62467683 | snp | G/T | 0.231189 | 0.249291 | intron-variant | ASB4 | GRCh38.p7 | 7:95525139 | TACAAGCCAAGAACT[G/T]CCAGCCATCACCAGA | 51666 |
rs62467696 | snp | C/T | 0.159951 | 0.233219 | intron-variant | ASB4 | GRCh38.p7 | 7:95529542 | ACAAACCAGAGAACT[C/T]TCAAATGAAGATTTG | 51666 |
rs62467697 | snp | A/G | 0.190833 | 0.242898 | intron-variant | ASB4 | GRCh38.p7 | 7:95533883 | CCTTCTTCCTCTCTC[A/G]TGCCTATTAGGATTT | 51666 |
rs62467698 | snp | C/G | 0.476746 | 0.10529 | intron-variant | ASB4 | GRCh38.p7 | 7:95534767 | ACTAGGTTGTAAACT[C/G]CTTAAAGACAAAAAA | 51666 |
rs63543363 | snp | C/G | | | | | GRCh38.p7 | 7:95468151 | ATTGGGTTGGGGGGG[C/G]CCCCATTCAACCTAA | 51666 |
rs66593445 | snp | G/T | 0.426507 | 0.177046 | intron-variant | ASB4 | GRCh38.p7 | 7:95497523 | AGGAAGAGGCACCTA[G/T]GTAGGGATAATCATT | 51666 |
rs66619691 | snp | A/G | 0.417845 | 0.185278 | | | GRCh38.p7 | 7:95481007 | GCAATAGGAACATTG[A/G]TTGGGAGTGTCAAGA | 51666 |
rs66947533 | snp | A/G | 0.386123 | 0.209692 | | | GRCh38.p7 | 7:95465829 | TACTCGGGAGATTGG[A/G]GTAAGAGGATTGCTT | 51666 |
rs67149513 | in-del | -/T | 0.3746 | 0.216737 | intron-variant | ASB4 | GRCh38.p7 | 7:95502107 | TCTCTCTTTTTTTTT[-/T]AGTTGTTAGCCTCAT | 51666 |
rs67223052 | in-del | -/C | 0.230603 | 0.249246 | intron-variant | ASB4 | GRCh38.p7 | 7:95520643 | CACTCCCACTCCCCA[-/C]CCCCCATCCCCATCC | 51666 |
rs71127410 | in-del | -/CACACA | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95513313 | ACACACACACACACA[-/CACACA]CACACACACACACAC | 51666 |
rs71127411 | in-del | -/AAAGAAAGAAAG | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95515232 | GAAAGAAAGAAAGAA[-/AAAGAAAGAAAG]AAAGAAAGAAAGAAA | 51666 |
rs71529809 | in-del | -/TC | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95500862 | ACCTGTGACCTCCCT[-/TC]CCAGCAATTGTGCTC | 51666 |
rs71529810 | in-del | -/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95507275 | CTAACTGGCTTTTTT[-/T]CTAGAGAGTCAAGAC | 51666 |
rs71719760 | in-del | -/A | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95488347 | CTCCGTCTCAAAAAG[-/A]AAAAAAAAAAGAAGT | 51666 |
rs71820298 | in-del | -/GT | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95493372 | AAAAAAGAGATGAAA[-/GT]GTGTGTGTGTGTGTG | 51666 |
rs71828281 | in-del | -/T | 0.23031 | 0.249223 | intron-variant | ASB4 | GRCh38.p7 | 7:95521796 | AATAGTATATTTTTT[-/T]AAATGGATACACATA | 51666 |
rs73235043 | snp | A/G | 0.482459 | 0.0919928 | | | GRCh38.p7 | 7:95463093 | TCTGTCACCTTGGGT[A/G]GAGTACAGTGGCATG | 51666 |
rs73235069 | snp | C/T | 0.12932 | 0.218944 | intron-variant | ASB4 | GRCh38.p7 | 7:95504131 | GGCTGCTAAGCAGCA[C/T]ATTATTTCTACCTAT | 51666 |
rs73235071 | snp | A/C | 0.449218 | 0.151037 | intron-variant | ASB4 | GRCh38.p7 | 7:95513101 | AGAGATTCTACCCAC[A/C]ATTGTTAGCTTTGAA | 51666 |
rs73235074 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASB4 | GRCh38.p7 | 7:95513158 | AAATGTGGGAAGCCT[C/T]TAGAAGCTGGAAAAG | 51666 |
rs73235076 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASB4 | GRCh38.p7 | 7:95514040 | CAGCTGTGCACTCAC[A/G]TGATCTCATCCTTGG | 51666 |
rs73235082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522643 | CTGTGTTGGTCCTCC[C/T]GTTTAGTACCAGTCT | 51666 |
rs73427774 | snp | A/G | 0.131723 | 0.220251 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471754 | ACTGCAGCTGGGGCA[A/G]AGGTAGCAGGTTAAT | 51666 |
rs73437888 | snp | G/T | 0.29046 | 0.246704 | | | GRCh38.p7 | 7:95481506 | CTGCTGAGAAAGTCA[G/T]GAGGCCCAAGGGGTT | 51666 |
rs73437893 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASB4 | GRCh38.p7 | 7:95488531 | GCAACAGCGTGGAGC[C/T]GAGCAGTCTACAGTG | 51666 |
rs73439820 | snp | A/C | 0.158962 | 0.232835 | intron-variant | ASB4 | GRCh38.p7 | 7:95521145 | CTTTTGCCTTCAATA[A/C]AAATTTTATCATTTC | 51666 |
rs73439825 | snp | C/T | 0.158632 | 0.232706 | intron-variant | ASB4 | GRCh38.p7 | 7:95525015 | CCTTCAAAGTGTCTG[C/T]GTGCCTAAATTAACC | 51666 |
rs73708299 | snp | G/T | 0.0535932 | 0.154675 | | | GRCh38.p7 | 7:95459709 | AACAGGCAGATATGA[G/T]TAAAGGGTTTTTGTC | 51666 |
rs73708302 | snp | C/T | 0.0452528 | 0.143452 | | | GRCh38.p7 | 7:95467372 | AAAATAGATGAATTA[C/T]TTTTTGTGAAAGCTC | 51666 |
rs73711304 | snp | A/G | 0.0456336 | 0.143994 | | | GRCh38.p7 | 7:95467591 | ACCTATACAGAAGAT[A/G]TGAACTTACACCTAC | 51666 |
rs73711306 | snp | G/T | 0.0726307 | 0.176182 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469105 | AGTTGTGTCTTCATT[G/T]GTTAAATGGGAAAGC | 51666 |
rs73711307 | snp | A/G | 0.0329836 | 0.124112 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470888 | CACCACCAAAGAAGA[A/G]AAAGAAATTAACATA | 51666 |
rs73711308 | snp | A/G | 0.0711525 | 0.174681 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471841 | ATGTGTGCTAACACT[A/G]TGCTTTCTTAGGCAG | 51666 |
rs73711309 | snp | A/T | 0.0263992 | 0.111815 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471996 | CCATTTCTTACTGAA[A/T]ACAAAGCAAAAAAAC | 51666 |
rs73711310 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472840 | TGGTCCACCCAGAAA[C/T]GTGCACTTCCCATCC | 51666 |
rs73711313 | snp | A/G | 0.030278 | 0.119257 | | | GRCh38.p7 | 7:95480947 | CTCAGTGATCAAATA[A/G]AATATCTAATTAACC | 51666 |
rs73711314 | snp | A/G | 0.0763149 | 0.179815 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484052 | AAAAAAAATTGTCAG[A/G]CATAGTGGCTCATGG | 51666 |
rs73711316 | snp | A/T | 0.00863278 | 0.0651296 | intron-variant | ASB4 | GRCh38.p7 | 7:95486204 | GTTAGAAAATGATTT[A/T]AAAAAATGCACAGTG | 51666 |
rs73711318 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASB4 | GRCh38.p7 | 7:95486336 | TTGTGGGCTGATATA[C/T]ATGTATAAGTCGTGT | 51666 |
rs73711321 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASB4 | GRCh38.p7 | 7:95487709 | ATGAGCTGACTCCTA[C/T]GGTCCTCATAGAGCT | 51666 |
rs73711323 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASB4 | GRCh38.p7 | 7:95489831 | GAAGTCAAGCACAGA[A/G]GAAATCTTTAAAGAA | 51666 |
rs73711326 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95499315 | TATGAAAAAGCCCCA[A/G]TGAATTCTAACATTT | 51666 |
rs73711327 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95500016 | GTAGCTGGGAGCATC[C/T]TCATTTTTAAGAAGC | 51666 |
rs73711328 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95500103 | ACGATGAGGGAGTTC[A/G]GATGGTTTTTCCCCT | 51666 |
rs73711329 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | ASB4 | GRCh38.p7 | 7:95501512 | CTTAATCATAAATAA[G/T]AACACTTAAGATCTA | 51666 |
rs73711331 | snp | C/G | 0.030278 | 0.119257 | intron-variant | ASB4 | GRCh38.p7 | 7:95502014 | CATAAAATTAAAAGG[C/G]AATCATAAAACTGGG | 51666 |
rs73711333 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | ASB4 | GRCh38.p7 | 7:95506825 | AAAATGTTCCTGAAT[G/T]ATTTCCTGGGTGAGT | 51666 |
rs73711334 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ASB4 | GRCh38.p7 | 7:95507249 | ATTGGTCAGATTCTC[C/T]GAAAAAAAATCTAAC | 51666 |
rs73711335 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ASB4 | GRCh38.p7 | 7:95509690 | GGAAATTGATGTTGC[C/T]GGTATACATGCATAT | 51666 |
rs73711337 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ASB4 | GRCh38.p7 | 7:95509884 | TGAATCAGGCCTCAG[C/T]ACAAAGCTTGTCAGA | 51666 |
rs73711338 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASB4 | GRCh38.p7 | 7:95511885 | GTCCACTAGGTGGTG[C/T]TGCCTTCCCTTTGCT | 51666 |
rs73711340 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ASB4 | GRCh38.p7 | 7:95520362 | ATTAACACTCTGTCT[A/G]CAAACTCAGGTTTAT | 51666 |
rs73711341 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ASB4 | GRCh38.p7 | 7:95520482 | GTGCCCATCAAAAGT[A/G]AATAAGTTGAGAGGG | 51666 |
rs73711343 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | ASB4 | GRCh38.p7 | 7:95529221 | TTTTATAGCTAGTAA[A/T]TAATTTGGAGGCCAA | 51666 |
rs73711344 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ASB4 | GRCh38.p7 | 7:95529998 | GGTAGAGCAATGAAC[A/C]AAAGGCCTTCATGAA | 51666 |
rs73711345 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | ASB4 | GRCh38.p7 | 7:95532511 | AGGAAAAGGTAACAC[A/G]AGGGTCTGGGAGAGG | 51666 |
rs73711346 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASB4 | GRCh38.p7 | 7:95533566 | TCTTGATCTTCATGA[C/T]CCCCTTGATAATCTC | 51666 |
rs73711347 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASB4 | GRCh38.p7 | 7:95534571 | CACCAGCCTGGGAGC[C/T]GGTTGGTGCACTTCC | 51666 |
rs73711348 | snp | C/T | 0.0252325 | 0.109451 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538909 | AGTGACAGTGGGCTA[C/T]GAAAAGTAAATAGAG | 51666 |
rs74320696 | snp | G/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95506706 | TTTTTTTTTTTTTTG[G/T]TCTTTGATGTTCTAA | 51666 |
rs74341719 | snp | A/C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517639 | AATGAGTCATCAATA[A/C/T]CATTAGATATAGTAG | 51666 |
rs74420394 | snp | C/T | 0.0352966 | 0.128072 | | | GRCh38.p7 | 7:95482847 | CTCACACACTTCTTC[C/T]GGGGTTGAACTTTGA | 51666 |
rs74438025 | snp | G/T | 0.5 | 0 | | | GRCh38.p7 | 7:95477748 | ACCTTTTTTTTTTTT[G/T]TTGCTATAATTCTGT | 51666 |
rs74441317 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASB4 | GRCh38.p7 | 7:95518922 | TCACTGGGAGTTAGT[A/G]AGATTATAGATAAGA | 51666 |
rs74577702 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517067 | CCCTGTGTTAATGAT[C/T]ATTTGCATGGTTTGT | 51666 |
rs74643962 | snp | A/G | 0.100588 | 0.200439 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468944 | GTTTTTGAACATGTT[A/G]TACAATCATACTTTC | 51666 |
rs74676887 | snp | G/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95493464 | TTTGGGTTGAGTTCA[G/T]TCATTCCTGTGGGAT | 51666 |
rs74780937 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472140 | GCTCAGTAGCTCATG[C/G]CATTTTGATTATCTA | 51666 |
rs74846459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501564 | ACAATGCAGTGTTAC[C/T]AACTATAGTCATCCT | 51666 |
rs74891973 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484528 | GTATACCTGTAACTT[A/G]CCAATTTCTTGCATT | 51666 |
rs74911514 | snp | A/G | 0.31721 | 0.240796 | intron-variant | ASB4 | GRCh38.p7 | 7:95521064 | ATTAATTCTGAAAGA[A/G]TTGCCATCTTTACAA | 51666 |
rs74990682 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | ASB4 | GRCh38.p7 | 7:95536661 | GAATGCCTTTAAAGC[A/G]TACTCAAATGCAATG | 51666 |
rs74997166 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | ASB4 | GRCh38.p7 | 7:95519792 | ATTAGTGATTTACTA[C/T]GTTTTAAGTCATGCA | 51666 |
rs75139643 | snp | A/G | 0.0655868 | 0.168795 | | | GRCh38.p7 | 7:95468272 | CACAACAAAAACCAA[A/G]ATGGGGTATAACACT | 51666 |
rs75149250 | in-del | -/ATAC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526460 | AACGCATTTTCATAC[-/ATAC]TTTCTCTAATAAATC | 51666 |
rs75163686 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ASB4 | GRCh38.p7 | 7:95529869 | GCTAAAGCTAATAGT[A/G]TTAATATATTTTCAT | 51666 |
rs75209527 | snp | A/G | 0.275464 | 0.2487 | intron-variant | ASB4 | GRCh38.p7 | 7:95498748 | AAAAATTTGTTTCAT[A/G]TGTTTATTTCTAGAG | 51666 |
rs75442893 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472841 | GGTCCACCCAGAAAC[A/G]TGCACTTCCCATCCC | 51666 |
rs75443247 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | ASB4 | GRCh38.p7 | 7:95518682 | GAACCACTAACTCAA[A/T]CTGAGTCCAACAAGA | 51666 |
rs75519228 | snp | A/G | 0.106633 | 0.204807 | intron-variant | ASB4 | GRCh38.p7 | 7:95530479 | CCAAAAGAAAAAATA[A/G]GGATGTGGAGGAACA | 51666 |
rs75539308 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95526773 | CAATAATAATAATAA[A/G]TCTGTACAGACTAAT | 51666 |
rs75588952 | snp | A/C | 0.0659589 | 0.169201 | | | GRCh38.p7 | 7:95482227 | TTAAATGAAAATTTG[A/C]TTTGTTTGTTTTCTT | 51666 |
rs75615757 | snp | A/C | 0.5 | 0 | | | GRCh38.p7 | 7:95465407 | TATGGAATCTAAAAA[A/C]TGACAGAGAAATATG | 51666 |
rs75699905 | in-del | -/CAGGTGGC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534078 | GCTGGGCGCGGTGGC[-/CAGGTGGC]TTACACCTGTAATCC | 51666 |
rs75805577 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510562 | AGATGTTAGCATTTT[G/T]CTTTTTTTCTCCAAA | 51666 |
rs75829565 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ASB4 | GRCh38.p7 | 7:95500832 | TTCCTCTGATCTCCA[A/G]CTGTAGATAATAGTG | 51666 |
rs76103523 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | ASB4 | GRCh38.p7 | 7:95527233 | TATGTGGTGGTGGTG[C/G]TGCTGCGTTCCAAGA | 51666 |
rs76111322 | snp | A/G | 0.0535932 | 0.154675 | | | GRCh38.p7 | 7:95480942 | GATTACTCAGTGATC[A/G]AATAGAATATCTAAT | 51666 |
rs76158640 | snp | A/G | 0.248188 | 0.249993 | intron-variant | ASB4 | GRCh38.p7 | 7:95496864 | AAACAAAAAACAAAG[A/G]ACAAAAACAAACAAA | 51666 |
rs76247746 | snp | G/T | | | | | GRCh38.p7 | 7:95467044 | TCTAGAACCACAAAA[G/T]AATGATTTTTTTCTG | 51666 |
rs76248585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507946 | ATGCAGAAGTCAGAG[G/T]GGGGGGGATTGAGAA | 51666 |
rs76270182 | in-del | -/TTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506702 | TTTTTTTTTTTTTTT[-/TTT]GGTCTTTGATGTTCT | 51666 |
rs76278080 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ASB4 | GRCh38.p7 | 7:95535885 | AGTTTACTTTACCTC[A/G]TGGTCACCAGTGAAT | 51666 |
rs76434215 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ASB4 | GRCh38.p7 | 7:95506742 | CACAATGAACTGTCT[G/T]GGTAGGTTTATCTTC | 51666 |
rs76440896 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | ASB4 | GRCh38.p7 | 7:95489407 | CAGCCTCCAGAGTTC[A/G]TGTTCAAACTGTGGA | 51666 |
rs76509698 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ASB4 | GRCh38.p7 | 7:95513081 | TCAGAGAGATAGGAT[A/G]TATAAGAGATTCTAC | 51666 |
rs76514895 | snp | A/G | 0.178144 | 0.239451 | intron-variant | ASB4 | GRCh38.p7 | 7:95493876 | TTTTTTAATGGTTGT[A/G]TAGTATTTGATTGAC | 51666 |
rs76557686 | snp | A/G | 0.00795532 | 0.062565 | | | GRCh38.p7 | 7:95483182 | CAGGGAGGGTCCAGA[A/G]GACAATGAGTCCATC | 51666 |
rs76580015 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASB4 | GRCh38.p7 | 7:95522345 | GAATTACAATATAAA[A/G]CACCTCTATCAGTTC | 51666 |
rs76796561 | snp | C/T | 0.00953873 | 0.0683987 | | | GRCh38.p7 | 7:95477852 | GGTTTTCTGAAAATA[C/T]GTGCCCCCTTTCTCT | 51666 |
rs76817274 | snp | A/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95488347 | CTCCGTCTCAAAAAG[A/G]AAAAAAAAAAGAAGT | 51666 |
rs76892510 | snp | C/T | 0.0667028 | 0.170006 | | | GRCh38.p7 | 7:95478760 | CCAAGCGAAGATGTG[C/T]TTGCGTAGGACTTTG | 51666 |
rs76955051 | in-del | -/T/TG | | | | | GRCh38.p7 | 7:95477750 | TTTTTTTTTTTTTTT[-/T/TG]GCTATAATTCTGTGA | 51666 |
rs76960815 | snp | C/T | 0.00929372 | 0.0675314 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528406 | GGCTTGAGTCCTGGG[C/T]TAACTACCTCTGATC | 51666 |
rs76982119 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510561 | TAGATGTTAGCATTT[A/T]TCTTTTTTTCTCCAA | 51666 |
rs76995473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95507250 | TTGGTCAGATTCTCC[A/G]AAAAAAAATCTAACT | 51666 |
rs76996770 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95534029 | GCTTTCTAATGGGGA[A/G]CATCTATTGTGTACA | 51666 |
rs77030194 | snp | A/G | 0.25912 | 0.249834 | intron-variant | ASB4 | GRCh38.p7 | 7:95530995 | TGCTGAAAGTTTCTG[A/G]GCCTCAGTTTCTTCC | 51666 |
rs77151416 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95521274 | AAGCCCAACCCAATG[A/C]AAAATGGGCAGAAGC | 51666 |
rs77315319 | snp | A/C | 0.0535932 | 0.154675 | | | GRCh38.p7 | 7:95460088 | TCCTGAGGCCTCCCC[A/C]AGCCATGTGGAATTG | 51666 |
rs77405895 | snp | C/T | 0.256897 | 0.249905 | intron-variant | ASB4 | GRCh38.p7 | 7:95503938 | CCATGCTGGATTTTG[C/T]CTGTTATTTTTCTGT | 51666 |
rs77423677 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ASB4 | GRCh38.p7 | 7:95499296 | ATATAGAGAAAAGTG[A/G]ATCTATGAAAAAGCC | 51666 |
rs77489547 | snp | A/G | 0.247337 | 0.249986 | intron-variant | ASB4 | GRCh38.p7 | 7:95494287 | TCATCGTAATATTCT[A/G]GATTTCTTATGACCT | 51666 |
rs77498638 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | ASB4 | GRCh38.p7 | 7:95486838 | CAAAAATTAGACCAA[-/T]TTTTTTTTACCAAGG | 51666 |
rs77511461 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472232 | CATTCTTTCCCCAAA[A/G]ATGTGTCCAAAATTG | 51666 |
rs77558301 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95509903 | AAGCTTGTCAGATTC[A/G]AGCAGATCAAATTTT | 51666 |
rs77594808 | snp | A/C | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95505697 | CGTGTCCCCCCCCCC[A/C]CAAATACTTATTCAT | 51666 |
rs77626949 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | ASB4 | GRCh38.p7 | 7:95499710 | AGGGAGGTCACAGGC[A/G]AGACTTACCTACAGT | 51666 |
rs77647948 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | ASB4 | GRCh38.p7 | 7:95487829 | CTGGAAAAGGAAAAG[A/C]ACAGTTCCATTCTTA | 51666 |
rs77703353 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525185 | CTGAGGCAGATTCTC[C/T]TCCAAAGTCTCTGGA | 51666 |
rs77703412 | snp | C/T | 0.0452528 | 0.143452 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474644 | CTTCTACCTCAGCCT[C/T]GTGAGTAGCTGAAAC | 51666 |
rs77708166 | snp | A/T | | | | | GRCh38.p7 | 7:95467047 | AGAACCACAAAATAA[A/T]GATTTTTTTCTGTGA | 51666 |
rs77728504 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASB4 | GRCh38.p7 | 7:95527433 | AGTGTTGTGACATAA[C/T]ATTTGTTTTTAATGA | 51666 |
rs77764354 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASB4 | GRCh38.p7 | 7:95512748 | GGCCTATAGCTAGAA[A/G]GGGAACTCACATTTG | 51666 |
rs77885147 | in-del | -/TTT | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473653 | TCCTTTTTTTTTTTT[-/TTT]AATCAACGGAATAAT | 51666 |
rs77889413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505242 | TAAATGGTTACAACT[A/G]GTAACTGAGTTCAGA | 51666 |
rs77945909 | snp | C/T | 0.0640965 | 0.167152 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474190 | AATATGCATATGTGC[C/T]GAACTTTAGTCTTTT | 51666 |
rs78004566 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASB4 | GRCh38.p7 | 7:95532160 | AGAAAGTCATCTTTA[C/T]GACAAGTAAGTGACT | 51666 |
rs78069824 | snp | C/T | 0 | 0 | | | GRCh38.p7 | 7:95463193 | GCACACCACCACACC[C/T]GGCCTATTTTTTAAA | 51666 |
rs78084603 | snp | C/T | 0.0663309 | 0.169604 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474368 | GATTTTTTAAAGAAC[C/T]AAAATTTACCAAAAG | 51666 |
rs78154769 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472326 | GACCAGATGCTTAGA[C/T]GAATGATCTGTTGCC | 51666 |
rs78263868 | snp | A/G | 0.0221141 | 0.102801 | | | GRCh38.p7 | 7:95482290 | ATTTATATAGCTATG[A/G]GACAAGACTGAAATA | 51666 |
rs78388943 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASB4 | GRCh38.p7 | 7:95519229 | ATGCTTTGGCGACAG[C/T]TCATGACATACTCGA | 51666 |
rs78429797 | snp | A/C | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95488441 | AAGTTAGGAATGGAA[A/C]TGACAAATAGAATCC | 51666 |
rs78446092 | snp | A/T | 0.0626037 | 0.165477 | intron-variant | ASB4 | GRCh38.p7 | 7:95487565 | GAAGTTTCTGAGGAT[A/T]TAAGAAACCAAGTTT | 51666 |
rs78481746 | snp | A/T | 0.16028 | 0.233346 | intron-variant | ASB4 | GRCh38.p7 | 7:95529641 | AACTAATTCTTTTTT[A/T]AAAAATTATATGTAA | 51666 |
rs78484758 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515161 | TTTCTTTCTTTCTTT[C/T]TCTTTCTCTTTCTTT | 51666 |
rs78512415 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539077 | CTTCACTTTTTTTTT[G/T]GTTCTTGCTATAATC | 51666 |
rs78550099 | snp | C/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95530442 | TGCACTTCACCCTGG[C/G]TGACAGAGCGAGACT | 51666 |
rs78635385 | snp | G/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95506702 | TTTTTTTTTTTTTTT[G/T]TTGGTCTTTGATGTT | 51666 |
rs78636293 | snp | A/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95534352 | CCATTAAAAAAAAAA[A/G]AGATGAACTATCCTC | 51666 |
rs78641443 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASB4 | GRCh38.p7 | 7:95495017 | TTCAAAGGCAAATTT[A/G]CAATGCCATTCTAGT | 51666 |
rs78650621 | snp | C/T | 0.0364509 | 0.129988 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471085 | TTCCTCAAAATGTTT[C/T]TCATTTTTCTGTCCC | 51666 |
rs78726942 | in-del | -/GGCC | 0.447291 | 0.153545 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472231 | CATTCTTTCCCCAAA[-/GGCC]AATGTGTCCAAAATT | 51666 |
rs78797132 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95518170 | AACTAGTTTTCACCA[A/G]TATCTTGTTCTCTTC | 51666 |
rs78826879 | snp | A/G | 0.493658 | 0.0559517 | intron-variant | ASB4 | GRCh38.p7 | 7:95493392 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 51666 |
rs79011268 | snp | G/T | 0.0539704 | 0.155153 | | | GRCh38.p7 | 7:95479637 | CCACTGATAAAATAT[G/T]CACTTTATTGCTTGT | 51666 |
rs79076343 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | ASB4 | GRCh38.p7 | 7:95499766 | GCTAAAGGAAATGAT[A/T]CATAGAAAGAAAACA | 51666 |
rs79091766 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489002 | AGTGAAAAGTAGTAC[A/G]ATCAATTCTAAACCA | 51666 |
rs79413724 | snp | C/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95535051 | ACACAGACACACTCA[C/G]TCACACACACACACA | 51666 |
rs79504713 | snp | A/G | 0.0391387 | 0.134304 | | | GRCh38.p7 | 7:95475225 | GGCTGTCAATAGAAT[A/G]GGTAGGGTCATATAC | 51666 |
rs79570110 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ASB4 | GRCh38.p7 | 7:95521818 | AAATGGATACACATA[C/T]AAATAGTAAAAAGAA | 51666 |
rs79579755 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95532418 | TTTTTTTCTCCCAGC[A/G]TAATTCAGAAGAAAG | 51666 |
rs79633262 | snp | A/G | 0.0221141 | 0.102801 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484707 | TTGACTTCCACAAAC[A/G]ACATATAAAAATGCA | 51666 |
rs79690239 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95517860 | ATAGAAAGAAATTGG[A/G]GGTTAGCTAAAAGGG | 51666 |
rs79880794 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASB4 | GRCh38.p7 | 7:95528988 | GATATCACACTGCAC[A/G]GTTTTTCTTAACAAC | 51666 |
rs80071828 | snp | A/G | 0.039522 | 0.134904 | intron-variant | ASB4 | GRCh38.p7 | 7:95500295 | ATGTGGCTAGGAGCC[A/G]TGGCTTATGCTTGTA | 51666 |
rs80073684 | snp | G/T | 0.0352966 | 0.128072 | | | GRCh38.p7 | 7:95482323 | TTCTGTGGGAAAAAT[G/T]ATAGCCATCTCTTTA | 51666 |
rs80083712 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95524906 | GTGGTAACCTGGGAT[C/T]CAGTCTGTAAGATGG | 51666 |
rs80137322 | snp | A/G | 0.155987 | 0.23165 | intron-variant | ASB4 | GRCh38.p7 | 7:95525218 | AAACCAACCCTAGAC[A/G]CTTTAATTTTGGACT | 51666 |
rs80143107 | snp | A/G | 0.030278 | 0.119257 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484903 | TTACTAGATTCACCA[A/G]GTCTTTAAGTTTTTG | 51666 |
rs80297058 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | ASB4 | GRCh38.p7 | 7:95525649 | CCCTTTGATTCTCTT[C/G]CTTACTGGAAATTCT | 51666 |
rs80300265 | snp | A/G | 0.163236 | 0.234461 | intron-variant | ASB4 | GRCh38.p7 | 7:95532348 | TACATAAGCGGGGGA[A/G]AAAAGAATTATAGGG | 51666 |
rs111237885 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95490818 | TAAACACACACGCGC[A/T]CGCGTGCACACACAC | 51666 |
rs111243297 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95497492 | GTGATGCCATTTTTT[G/T]AGGTAAAGAAACTTG | 51666 |
rs111246561 | snp | G/T | 0.0170251 | 0.090679 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474407 | CTCACTTATCAATTT[G/T]TTTTTTTTATATCTC | 51666 |
rs111258249 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ASB4 | GRCh38.p7 | 7:95532039 | ACAGACTGTGTAGGA[A/G]AGCTGGCCCCCCTCC | 51666 |
rs111401235 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | ASB4 | GRCh38.p7 | 7:95515509 | CAACCTCTGCATCCC[A/G]TGTTCAAGTGATTCT | 51666 |
rs111427892 | snp | A/C | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95480615 | GAGAACTACATGGAC[A/C]CAAACCACATAACCA | 51666 |
rs111583180 | snp | G/T | 0.5 | 0 | | | GRCh38.p7 | 7:95460737 | AAGTTGCACAAGTAA[G/T]GAGGAGCCAAATGTT | 51666 |
rs111654837 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95522885 | TAATTCTAGACTAGT[C/T]CTGGAGACCCTCTTG | 51666 |
rs111656146 | snp | A/T | 0.5 | 0 | | | GRCh38.p7 | 7:95462709 | GCAAAAAATACTAAT[A/T]TTAGCAAAAATGTAT | 51666 |
rs111740338 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASB4 | GRCh38.p7 | 7:95532013 | ATTACAAACATTTTT[A/G]TTGCTACTCAACAGA | 51666 |
rs111750902 | snp | C/T | 0.0130921 | 0.0798413 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473718 | AGAGGATTGAAGAAG[C/T]GGTTCCTGTTTTTGA | 51666 |
rs111785503 | in-del | -/CATA | 0.263535 | 0.249633 | intron-variant | ASB4 | GRCh38.p7 | 7:95526455 | TTTGCAACGCATTTT[-/CATA]CATACTTTCTCTAAT | 51666 |
rs111801232 | snp | A/C | 0.5 | 0 | | | GRCh38.p7 | 7:95476562 | ACCAGGGCTGGGAAA[A/C]GGGAACAATATCTTT | 51666 |
rs111858857 | in-del | -/A | 0.5 | 0 | | | GRCh38.p7 | 7:95479098 | TGTTCCATAAGGGAG[-/A]AAAAAAGCCCTAAAG | 51666 |
rs111917269 | in-del | -/A | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95517612 | ACTGAAAAAAAAAAA[-/A]GAATTTCAAGAAATG | 51666 |
rs111964010 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502400 | AGCCTGCGGGGGGGG[A/C/G]GCAAATTGATAACAC | 51666 |
rs111979804 | snp | C/G | 0.301681 | 0.2446 | | | GRCh38.p7 | 7:95463076 | AAGAGACAAGGTCTT[C/G]CTCTGTCACCTTGGG | 51666 |
rs112031292 | snp | A/C | | | | | GRCh38.p7 | 7:95468665 | TTTAACCGTCATTTA[A/C]TTTTGTACAAAATTC | 51666 |
rs112039704 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ASB4 | GRCh38.p7 | 7:95508980 | CGACTCAGTCCAGGT[A/T]TGACTGTGGGTTGGA | 51666 |
rs112046246 | snp | C/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95536363 | TGGTCTGTGAATTCT[C/T]GATGTCTCTGTGAGC | 51666 |
rs112097711 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | ASB4 | GRCh38.p7 | 7:95525383 | AGTTGATGTTTCTGG[C/T]CTCTAATTTATTGAA | 51666 |
rs112112199 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95522625 | GGGTTGGGAAGCACT[C/T]ATCTGTGTTGGTCCT | 51666 |
rs112181689 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASB4 | GRCh38.p7 | 7:95521152 | CTTCAATAAAAATTT[C/T]ATCATTTCCTTCATA | 51666 |
rs112194688 | snp | C/T | 0.5 | 0 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536545 | ATCCCCGATGATGAC[C/T]TGGAGGTAAATAATC | 51666 |
rs112210069 | snp | G/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95496433 | ATATATAATTATAAA[G/T]TGGGACAGTGTTTTG | 51666 |
rs112225381 | snp | C/T | 0 | 0 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470436 | TTTTTTTAAAAAAAA[C/T]TCTTAATCCATAGAT | 51666 |
rs112279792 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95527111 | TGAATATTTCTACTA[C/T]ACCAGCTTCTGCCCC | 51666 |
rs112363198 | snp | A/C | 0.153332 | 0.230554 | intron-variant | ASB4 | GRCh38.p7 | 7:95504350 | CAGTGACACAAGTCA[A/C]CCACATGTTAGGAAA | 51666 |
rs112368124 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488292 | CTTGCAGTGAGCCCA[A/G]ATGGCGCCACTGCAC | 51666 |
rs112373734 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASB4 | GRCh38.p7 | 7:95532951 | TCCCTTTGGGGTCCA[C/T]ATCAGTCTGCTGTCT | 51666 |
rs112442635 | in-del | -/TGTGTGTGTG | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95513294 | ATCGAGCCAATAGAA[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 51666 |
rs112450020 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95526154 | GGTGGAATAGAACAG[A/T]GATAAGGAATTTCGA | 51666 |
rs112535560 | snp | A/C | 0.0693013 | 0.172766 | intron-variant | ASB4 | GRCh38.p7 | 7:95530451 | CCCTGGGTGACAGAG[A/C]GAGACTCTGTCTCCA | 51666 |
rs112538412 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASB4 | GRCh38.p7 | 7:95519653 | TATAGTAAATGGAAC[C/T]GAATTCCTTCTCAAA | 51666 |
rs112547068 | snp | A/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95536302 | CAATCCTCCTGCCTC[A/T]GTCTCCCAAGTAGCT | 51666 |
rs112599911 | snp | A/G | 0.5 | 0 | missense | ASB4 | GRCh38.p7 | 7:95528047 | GCATGCTGCTTGACT[A/G]CAAAGCCGAAGTCAA | 51666 |
rs112615914 | snp | A/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95536043 | CAAAGTAATTCTTCA[A/G]TTCTCATCTTCTTTG | 51666 |
rs112692816 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASB4 | GRCh38.p7 | 7:95531990 | TTGGCTACTGGTAGA[C/T]GGCTGGTATTACAAA | 51666 |
rs112694034 | snp | G/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95514979 | CTTTATGTAGCCATA[G/T]CTCTAGTTTCACCAG | 51666 |
rs112699869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95490066 | TTTTATTAATCAGGG[G/T]AATGCACTTTAAGTA | 51666 |
rs112769333 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | ASB4 | GRCh38.p7 | 7:95497625 | CATTTTGAGAAATAT[G/T]GTTTTTGTGAAACTA | 51666 |
rs112794740 | snp | A/C/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95505696 | CCGTGTCCCCCCCCC[A/C/G]CCAAATACTTATTCA | 51666 |
rs112811609 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483565 | CCCATAATGGGGGAT[C/G]AGATCAAATGATTAG | 51666 |
rs112815871 | snp | A/G | 0.0115144 | 0.0749975 | | | GRCh38.p7 | 7:95482762 | GTAGCTAGGAAGGCT[A/G]GAAGTCTTGATGGAT | 51666 |
rs112828523 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471780 | TTAATACCAGCTAAC[A/G]CCTCCAGAGCATTTG | 51666 |
rs112833775 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASB4 | GRCh38.p7 | 7:95497209 | TTAAAGTCATTATTC[C/T]GGAGCTATGCAGAAA | 51666 |
rs112854772 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ASB4 | GRCh38.p7 | 7:95494701 | ATGGCTATTGGCATT[C/G]ACATAGAAAGAAGGT | 51666 |
rs112930653 | snp | A/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95536085 | TTTTCACTTGCTCGT[A/G]GAAGGTGAAAGAAAT | 51666 |
rs113016443 | snp | C/T | 0.20111 | 0.245173 | | | GRCh38.p7 | 7:95460278 | AGGAAGAGGTTGGAA[C/T]AGTTTGGAGGGCTCA | 51666 |
rs113043276 | snp | A/G | 0.0130921 | 0.0798413 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95472052 | TGTCCTCATACTCAC[A/G]GCAAAAGGAGGTCAG | 51666 |
rs113050249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526025 | ACAATACATGGTAAA[C/T]GGATTTTTTTTAAAG | 51666 |
rs113084935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533366 | AAATTACTTATTGGG[C/T]TTCTAACACTCTTCG | 51666 |
rs113127686 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469744 | CATTGCTCGTTCATA[A/G]AAAATAAAGTTATTG | 51666 |
rs113180710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95497031 | TGACCAGAGTATCAT[A/G]GGTGTGGGGTAGGGT | 51666 |
rs113199359 | snp | C/T | 0.5 | 0 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471322 | TTGTCCTCTTTCCTG[C/T]ACGCTTCCTCATTTG | 51666 |
rs113270292 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASB4 | GRCh38.p7 | 7:95508250 | AGAGGAGAACCTCTG[C/T]TCTATCGTAGCCAGA | 51666 |
rs113293801 | snp | A/C | 0.00914312 | 0.0669923 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474544 | TTTTTCTTTTTGAGA[A/C]AGGGTCTCATTCTGT | 51666 |
rs113298569 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | ASB4 | GRCh38.p7 | 7:95535132 | ATAACCTTTCTGTCT[C/G]TGTTTTATCTGTGAT | 51666 |
rs113316275 | snp | G/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95513253 | TTTTGTTTTTTGTTT[G/T]TTTTTTTTTTTTTTT | 51666 |
rs113367065 | snp | A/C/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95486541 | CCTGGTTTAAGAACA[A/C/T]GCTGCTAATTCTCCA | 51666 |
rs113445910 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ASB4 | GRCh38.p7 | 7:95511906 | TCCCTTTGCTACTTT[A/G]GAGTCCTGCCGCTAA | 51666 |
rs113470979 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASB4 | GRCh38.p7 | 7:95516357 | TTTTTGGAATTAAAA[A/G]GATAAAAAATAAAAT | 51666 |
rs113583710 | snp | A/T | 0.5 | 0 | | | GRCh38.p7 | 7:95468135 | ATTATTTTTTTATTA[A/T]ATTGGGTTGGGGGGG | 51666 |
rs113615285 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499895 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTCGCTTTG | 51666 |
rs113642166 | snp | C/T | 0.4776 | 0.103433 | intron-variant | ASB4 | GRCh38.p7 | 7:95515165 | TTTCTTTCTTTCTCT[C/T]TCTCTTTCTTTCTTT | 51666 |
rs113668289 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95501646 | TTGTTAACTTTTTAC[A/T]TTGTGGCCTTTTCAT | 51666 |
rs113692909 | snp | A/C | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95480409 | TCCTGGTTTTCACAC[A/C]TTTAACAAAATCCTC | 51666 |
rs113706540 | snp | C/T | 0.158302 | 0.232576 | | | GRCh38.p7 | 7:95475633 | AGGTGATCCACCCAC[C/T]TCAGCTTCCCAAAGT | 51666 |
rs113724749 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 7:95467253 | GCAATAGTATAGCCT[A/G]CTGCTACCCTCTTCA | 51666 |
rs113746006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95490283 | CACCTAATTTTCCTC[C/T]TTGCCAGAAATTCAC | 51666 |
rs113773272 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95511603 | GGAGGCCGAGGGTGC[A/G]GTGAGCCGAGATTGC | 51666 |
rs113786528 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | ASB4 | GRCh38.p7 | 7:95520881 | TTTGATATTTGGTGG[G/T]GTAAGTACCCCTTAT | 51666 |
rs113857025 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | ASB4 | GRCh38.p7 | 7:95530372 | TGGGAGGCTGAGGCA[C/G]GAGAATGGCTTGAAC | 51666 |
rs113888681 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASB4 | GRCh38.p7 | 7:95524562 | GTGTTATGGGTCGAA[C/T]TGTGCGCCACCCCCC | 51666 |
rs113928706 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95521501 | ACACTGATGAATATA[A/G]TTTAATATGGTTGAA | 51666 |
rs113940182 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485004 | TATATATGTATATAT[A/G]TGTGTGTATATATGT | 51666 |
rs113967857 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ASB4 | GRCh38.p7 | 7:95505692 | CTATCCGTGTCCCCC[C/G]CCCCCCAAATACTTA | 51666 |
rs113969641 | snp | A/G | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95534859 | CTTAATGGAATGGAT[A/G]GGTTGAATATCATCC | 51666 |
rs113970910 | snp | C/T | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95536362 | CTGGTCTGTGAATTC[C/T]TGATGTCTCTGTGAG | 51666 |
rs113971437 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95525474 | AAAAGTTACACTGGC[A/G]ACACAATTCAAGTAT | 51666 |
rs114154312 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95493928 | AGCAATCTCCTATCA[A/G]TTAACATGGAGGTTG | 51666 |
rs114174452 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASB4 | GRCh38.p7 | 7:95486348 | ATATATGTATAAGTC[A/G]TGTCTCTCCTTTTCT | 51666 |
rs114221737 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95496619 | TTGGAGGCTAAGGTG[A/G]GAGGATCACTTGAGC | 51666 |
rs114222315 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95467074 | GTGAACTTATATATA[C/T]GTAAACAGCTTACCA | 51666 |
rs114251976 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASB4 | GRCh38.p7 | 7:95524314 | CAAATGAGAACTAAA[C/T]AGCACAAGACAGATT | 51666 |
rs114296603 | snp | C/T | 0.000313751 | 0.0125211 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495781 | TTGCCTAGCTATAAA[C/T]TGAAGTCTTCCTGGG | 51666 |
rs114441292 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95491112 | CTCTCTAAGTTCAGA[A/T]TCTGGCATGCAGATA | 51666 |
rs114494186 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95492334 | AGCAAATGCATTTCC[A/G]TATCAGAGATGTGAA | 51666 |
rs114649731 | snp | A/C | 0.0154538 | 0.0865337 | | | GRCh38.p7 | 7:95480875 | GGCTCATAGTAAGTT[A/C]CCAAAAAATATTTAT | 51666 |
rs114649886 | snp | C/T | 0.0221141 | 0.102801 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484939 | CTTGCTATCTCTCTG[C/T]TTCTATTTACACACA | 51666 |
rs114696574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95524553 | GTATGTTATGTGTTA[C/T]GGGTCGAATTGTGCG | 51666 |
rs114745554 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95460940 | AAGCTCCAGCCATGG[C/T]TAATAGGGGCCAATG | 51666 |
rs114951738 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASB4 | GRCh38.p7 | 7:95496150 | CCAGATGATGTAGTA[A/G]GCATAAAGATGCAAT | 51666 |
rs115023850 | snp | A/T | 0.0667028 | 0.170006 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539815 | GATGGGTGCACTAAA[A/T]TCTCAAAATTCACCA | 51666 |
rs115138317 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95465906 | GTAACCACTGTACTC[C/T]AGCCTAGGCAACATA | 51666 |
rs115182268 | snp | C/G | 0.0126979 | 0.078662 | | | GRCh38.p7 | 7:95479031 | TCTCAGCAAGGTCTT[C/G]TGCCCTTGCAAAATG | 51666 |
rs115266238 | snp | A/G | 0.0115144 | 0.0749975 | | | GRCh38.p7 | 7:95482117 | GCTTTGTAGGTGCAA[A/G]TAATCTGTAAGTTTT | 51666 |
rs115325713 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95499384 | TAAGATATACTGATA[A/C]GTAAAATTGGAGAAA | 51666 |
rs115373925 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ASB4 | GRCh38.p7 | 7:95527472 | AATATCATTGTTATG[C/T]TGATTAAGAAGATTT | 51666 |
rs115414322 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASB4 | GRCh38.p7 | 7:95521979 | CTAAAGCAAATATGG[C/T]AATAATTAAATTCAG | 51666 |
rs115457619 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95514830 | AAGTCTTTTGCTTAA[G/T]TCCATCCAAAGTGTG | 51666 |
rs115527465 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95489279 | GGAAGACAGAATAAA[A/G]CTATTGGATTACAAA | 51666 |
rs115671369 | snp | A/G | 0.0174175 | 0.0916809 | | | GRCh38.p7 | 7:95460160 | TGGGTATTTCTTCAC[A/G]GTAGCATGAGAATGG | 51666 |
rs115719288 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | ASB4 | GRCh38.p7 | 7:95490355 | CTTCGATGTTCAAAC[A/T]TTTTTCTTTTACATT | 51666 |
rs115722837 | snp | A/G | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95459804 | TGTCGGTGACTACTG[A/G]TGTTTCTAGATTGTG | 51666 |
rs115739885 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ASB4 | GRCh38.p7 | 7:95508452 | GAAATATTATATTTT[A/C]TATAATTATAGAGAA | 51666 |
rs115830213 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ASB4 | GRCh38.p7 | 7:95526950 | GAAAAACAAAATTCA[A/C]TTAAGTTTTCTAGTC | 51666 |
rs115894826 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95495190 | GTCTTTGGAAAGCGA[A/T]ATTGCATAAATCAAC | 51666 |
rs115945076 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473394 | GGCACAGAGAGGGTA[A/G]GCAGTTAAGTCAGGA | 51666 |
rs115994006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497744 | TGTCCCTATAATTTT[G/T]CCTGTTTTCAGAATG | 51666 |
rs116006847 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95459742 | TGGGCTGCCTCTTTC[C/T]TCATCCTCTGGCTAG | 51666 |
rs116060295 | snp | A/G | 0.0150606 | 0.0854603 | | | GRCh38.p7 | 7:95459639 | ACTGGTTCTGCCACT[A/G]CAGTGCCATTGTGGT | 51666 |
rs116061769 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95463532 | TTAGTGCTGCTCTTG[C/T]GGTAGAGTTCTTACA | 51666 |
rs116151641 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95464502 | ATGCTTAAACATCGC[C/T]CATATTTTGTAATTA | 51666 |
rs116179696 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | ASB4 | GRCh38.p7 | 7:95486756 | TTTTTTCCTGGACTA[A/C]AATAATTGTTCAAAA | 51666 |
rs116210868 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95518041 | GGTCTTAAATTGGAG[A/G]AGAGACCCTACTTCC | 51666 |
rs116236008 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASB4 | GRCh38.p7 | 7:95513075 | GGAAGGTCAGAGAGA[C/T]AGGATGTATAAGAGA | 51666 |
rs116264737 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | ASB4 | GRCh38.p7 | 7:95527022 | TCCAAGTACAAAAAA[A/T]TCCTATTTCTAACAT | 51666 |
rs116318239 | snp | C/T | 0.039522 | 0.134904 | | | GRCh38.p7 | 7:95482502 | ATCAGCTTTAAGTCT[C/T]AATGCAGACACTTAC | 51666 |
rs116318733 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95509365 | CATCCCACATCCGTT[C/G]TTTGAGCTTGGAACA | 51666 |
rs116345752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529182 | AGTGCTACAGAAATA[C/T]GGAAGAGAGTGAATT | 51666 |
rs116518491 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95496697 | ACAAAAAGCAAAAAA[A/C]ATTAGCCGGGCATGG | 51666 |
rs116549065 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468986 | CAGTACAAAAAATAA[C/T]TTATCTGTAAGAGAG | 51666 |
rs116549850 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ASB4 | GRCh38.p7 | 7:95507955 | TCAGAGTGGGGGGGA[C/T]TGAGAACTAAAAAGG | 51666 |
rs116605406 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95493892 | TAGTATTTGATTGAC[A/G]GATGTATCATAATTT | 51666 |
rs116606928 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASB4 | GRCh38.p7 | 7:95498385 | CATTAGAATGTTAGC[C/G]ATTCTAAATATGTTT | 51666 |
rs116608558 | snp | G/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95460094 | GGCCTCCCCCAGCCA[G/T]GTGGAATTGTAGGTC | 51666 |
rs116639680 | snp | G/T | 0.0225045 | 0.103662 | | | GRCh38.p7 | 7:95476103 | GCACAGTAGATTCTG[G/T]TCTGCCTTATTGTAT | 51666 |
rs116721715 | snp | C/T | 0.0352966 | 0.128072 | | | GRCh38.p7 | 7:95480608 | CAATGGAGAGAACTA[C/T]ATGGACACAAACCAC | 51666 |
rs116749558 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95487520 | GACTGTCTTCTCTCA[G/T]CTGAGCAGGCCAAGT | 51666 |
rs116749734 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ASB4 | GRCh38.p7 | 7:95525370 | CAAAGTTCCCAGGAG[C/T]TGATGTTTCTGGTCT | 51666 |
rs116833145 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95493670 | TAACAAGAACAAGTG[C/T]ATTTCTGTCCTGATC | 51666 |
rs116847760 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ASB4 | GRCh38.p7 | 7:95517782 | ACTGAGGAGTGTATC[A/G]GTGGTGAGACAGTGG | 51666 |
rs116848537 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASB4 | GRCh38.p7 | 7:95494087 | AATACAGTGGTCCTT[C/T]AGGACATTTCACATG | 51666 |
rs116886372 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | ASB4 | GRCh38.p7 | 7:95504437 | AATCCGAAATAGATA[G/T]GCCTGCTGGACAGAC | 51666 |
rs116894508 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95467887 | CTCCAGCATGAAACA[A/G]CTCACCAATTAACAT | 51666 |
rs116922441 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ASB4 | GRCh38.p7 | 7:95505406 | ATATTTAGCAAAAGA[A/G]GTGGAAGAAATATGA | 51666 |
rs116960695 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASB4 | GRCh38.p7 | 7:95525894 | AGCAATGTACTCTTG[A/G]GTACCTTCCTTGGGG | 51666 |
rs116967616 | snp | G/T | 0.0364509 | 0.129988 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471551 | GTATGAGAGTTGAAG[G/T]CTCTTCCAACACTGT | 51666 |
rs117023186 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ASB4 | GRCh38.p7 | 7:95507018 | CTGTTTTTATTGTCT[C/G]TGTCAACTATATTAG | 51666 |
rs117023763 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | ASB4 | GRCh38.p7 | 7:95494677 | TCCATTCATAAAAGC[A/T]TAAATGCTATGGCTA | 51666 |
rs117050469 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95524015 | ATAAGGATGTAATAC[A/G]ATGAGAAACCCTCAC | 51666 |
rs117099717 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ASB4 | GRCh38.p7 | 7:95506243 | TTAAACTCAGTGGGT[A/G]TTTTATCAATGTTAT | 51666 |
rs117134714 | snp | A/G | 0.095 | 0.19615 | | | GRCh38.p7 | 7:95468756 | TAATGAGCAGTAAAC[A/G]CATGTCCAAGTCCTG | 51666 |
rs117228167 | snp | A/G | 0.00318978 | 0.0398085 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473921 | GGATGGAAAGAAGGA[A/G]CCGGATGGCTTTGGG | 51666 |
rs117230776 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ASB4 | GRCh38.p7 | 7:95500492 | AATTGCTTGAGCTCA[C/T]GAGTTTGAGGCTGGC | 51666 |
rs117304132 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95523870 | AGTAATATAAAAGCA[C/T]TGTTGGTCAGTAAAA | 51666 |
rs117305001 | snp | A/T | 0.0517044 | 0.152246 | | | GRCh38.p7 | 7:95461052 | GCTGCAGGGGCAAAG[A/T]CCTCATGGAGAACAT | 51666 |
rs117314645 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ASB4 | GRCh38.p7 | 7:95522320 | GATGGCAATGATGCT[C/T]GTGGTGTTTGAATTA | 51666 |
rs117333618 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ASB4 | GRCh38.p7 | 7:95522321 | ATGGCAATGATGCTC[A/G]TGGTGTTTGAATTAC | 51666 |
rs117393944 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ASB4 | GRCh38.p7 | 7:95530062 | AAACAACAACCAAAT[A/G]AATATACTCTGATAT | 51666 |
rs117424662 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASB4 | GRCh38.p7 | 7:95535067 | TCACACACACACACA[C/T]GCACATGCACACACA | 51666 |
rs117472925 | snp | A/G | 0.0387552 | 0.1337 | | | GRCh38.p7 | 7:95482639 | TAGGGTTTCTTTCAC[A/G]AGGCAAAGATGATAA | 51666 |
rs117474846 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95512451 | AATGCGTTTCCCAAA[A/G]TCCACTGTATTAAGC | 51666 |
rs117478649 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95507150 | TTTGTTTGTTTGTTT[G/T]TTTTTTTGCTGCAGG | 51666 |
rs117480808 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538818 | TGTGAGGGGACCTAG[C/T]TGATTACTTCGGTCT | 51666 |
rs117554412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533852 | AAGTCCTCGAAAAAT[G/T]GTAGCTATTATTTTC | 51666 |
rs117601773 | snp | G/T | 0.039522 | 0.134904 | | | GRCh38.p7 | 7:95477696 | TGGCCTCAGTACTTT[G/T]TTTCTTAAATGAGAA | 51666 |
rs117666228 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ASB4 | GRCh38.p7 | 7:95501932 | ATGTCATCAAAGGCC[A/G]AATTCACAAAGAAAA | 51666 |
rs117683503 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95513929 | TTCTGCCATCATCCA[C/T]GAAGGATTTCGATGC | 51666 |
rs117693635 | snp | A/G | 0.0209421 | 0.100162 | | | GRCh38.p7 | 7:95462743 | TCAAGTAGTATTAGC[A/G]TTTGAATAACTAAAA | 51666 |
rs117717453 | snp | A/C | 0.0345262 | 0.126772 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538191 | TAAACTTGGTGTTTT[A/C]CCCCATTACCCCTTA | 51666 |
rs117755498 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95521200 | CTGATTATGTTTTCA[A/G]TACATAAAGAAATGT | 51666 |
rs117835667 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ASB4 | GRCh38.p7 | 7:95517077 | ATGATCATTTGCATG[A/G]TTTGTTCTTGTAGAA | 51666 |
rs117853851 | snp | C/T | 0.0391387 | 0.134304 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485433 | TCAAGTCTAGGTCAC[C/T]TGAAAACCTCCTGTT | 51666 |
rs117962784 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ASB4 | GRCh38.p7 | 7:95508729 | TGAAGAGATGAAGGG[A/T]ATTTAAAGTTCCAGC | 51666 |
rs118061692 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539144 | TTAGAGGTTAAAGCA[A/G]AAGTAAATTGCAAAC | 51666 |
rs118130785 | snp | G/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95464491 | GCTTGAAAATAATGC[G/T]TAAACATCGCCCATA | 51666 |
rs137919051 | in-del | -/GGTGGCCA | 0.161924 | 0.233971 | intron-variant | ASB4 | GRCh38.p7 | 7:95534072 | TGAATGGCTGGGCGC[-/GGTGGCCA]GGTGGCTTACACCTG | 51666 |
rs137946470 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481467 | AATCATCCATTTCTG[C/T]AATAGCAAGGACATC | 51666 |
rs138005988 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476393 | TGACATTCTTTTTTA[C/T]ATTTAAAAAAAAATT | 51666 |
rs138024864 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ASB4 | GRCh38.p7 | 7:95534174 | ACATGGTGAAACCTC[A/G]TCTCTGCTAAAAATG | 51666 |
rs138139149 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538725 | ATACTTTCCCAGACT[C/T]CTTGAGAAAAATATT | 51666 |
rs138170525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491030 | ATATGAACATGGACA[C/G]TTTATACTACTTAAC | 51666 |
rs138256660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95499635 | AGGTAAACAATTGGT[A/G]AAAAGAAGTGAGGCT | 51666 |
rs138279078 | in-del | -/AC | 0.0360663 | 0.129354 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484948 | TCTCTGTTTCTATTT[-/AC]ACACACATATATATA | 51666 |
rs138295168 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95505961 | TGCAGTGGCATGACC[A/G]TGGTTCACTGCAGGT | 51666 |
rs138319200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493692 | GTCCTGATCCCCCAA[A/C]CCCCCAGTTCTTCTT | 51666 |
rs138337588 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528099 | ATCTCCCCTCCACAA[A/G]GCAGCCTGGAACTGT | 51666 |
rs138342161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535101 | GCACACTCTTACTTA[G/T]TTGGATATTAAGATC | 51666 |
rs138353428 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492288 | TCTTTAGGTGCTACC[C/T]GGAAGTTAGGAGGAG | 51666 |
rs138454369 | snp | C/T | 1.70032e-05 | 0.0029157 | missense | ASB4 | GRCh38.p7 | 7:95527816 | TTCCCTTTATAGGGG[C/T]GAATGTGAACATGAA | 51666 |
rs138516415 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469712 | GAGAACAACAGTAAT[A/G]CATTTAATTGTTGGT | 51666 |
rs138545887 | in-del | -/G | 0.0528381 | 0.153711 | intron-variant | ASB4 | GRCh38.p7 | 7:95486376 | TCTTTTCCCACCCTT[-/G]GGCCTAGGACTTGAA | 51666 |
rs138567471 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464497 | AAATAATGCTTAAAC[A/G]TCGCCCATATTTTGT | 51666 |
rs138578271 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95487342 | TTAGAAAATTTGTAT[A/G]CTATATAATCAGATT | 51666 |
rs138592628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528530 | AGAAAAAGAGTAGCA[A/C]ATAATTTGTTTTGCC | 51666 |
rs138592722 | snp | C/T | 0.00159617 | 0.0282053 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471212 | CTACAGGAAAAAAGA[C/T]GCACGTCCCCTTCAA | 51666 |
rs138641653 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95524551 | ACGTATGTTATGTGT[C/T]ATGGGTCGAATTGTG | 51666 |
rs138706237 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493228 | TCATACTTTAAACAA[A/T]CCTCAGTCCATTAGA | 51666 |
rs138743651 | snp | A/G | 6.59761e-05 | 0.00574314 | missense | ASB4 | GRCh38.p7 | 7:95527999 | TCCGCTTTAAGGAGC[A/G]GGAGTACAGCACGGA | 51666 |
rs138769427 | in-del | -/T | 0.077417 | 0.180873 | | | GRCh38.p7 | 7:95462243 | TGATATAAATATATA[-/T]TATTTTTGGTCCAGG | 51666 |
rs138869176 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538256 | ACTCCCCAAACCAAG[C/T]TACTCAAGTTTATTT | 51666 |
rs138884506 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95505694 | ATCCGTGTCCCCCCC[A/C]CCCCAAATACTTATT | 51666 |
rs138935175 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASB4 | GRCh38.p7 | 7:95534753 | GTCTTTTCTCTTCAA[C/T]TAGGTTGTAAACTGC | 51666 |
rs138952846 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95475297 | CATAGTCCCTCCCCA[C/T]GCCCACCTGGATGTA | 51666 |
rs138954477 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95500270 | GATTACTGGACTTAT[A/C]AAAGATGCCATGTGG | 51666 |
rs139062336 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466000 | CCAATTAGAATAGTG[A/C]AATTTAAGTATGATA | 51666 |
rs139162949 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95509244 | GAAGTAGGGGTGTTC[A/T]TTTTATTTATCTTTC | 51666 |
rs139204724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95525606 | GATGTGGTTTGTTCC[A/G]AGTTGGCCTGTAAGA | 51666 |
rs139290146 | snp | A/G | 0.000153988 | 0.00877328 | stop-gained | ASB4 | GRCh38.p7 | 7:95536520 | ATGGAACACAAAGTG[A/G]AGAAGAGCTATCCCC | 51666 |
rs139339596 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95489375 | TTACCAATTTGGCAG[A/C]GAACAGATTTAGAAG | 51666 |
rs139351620 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ASB4 | GRCh38.p7 | 7:95511881 | TTTTGTCCACTAGGT[G/T]GTGCTGCCTTCCCTT | 51666 |
rs139353681 | snp | C/T | 0.00119737 | 0.0244387 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471961 | AGTATTGAGTCTATA[C/T]GCTTAAGTATTGTGC | 51666 |
rs139417372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507317 | TATTCCAGGTGCTAA[A/G]TTAGGGGAAAAGGCT | 51666 |
rs139420182 | snp | C/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95466898 | AACAGCATGGAAAAA[C/T]CTGCACCCATGATTC | 51666 |
rs139445299 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95495187 | TTCGTCTTTGGAAAG[A/C/T]GATATTGCATAAATC | 51666 |
rs139483916 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | ASB4 | GRCh38.p7 | 7:95501866 | TTAGGCTTATAAGAA[A/T]CAAGGAGAGAGAATA | 51666 |
rs139595390 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462126 | GGCCAAGGTATTTAT[A/G]AGGCAACAAAATACT | 51666 |
rs139597620 | snp | C/T | 0.000131907 | 0.00812009 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537641 | CTCTCATGCACTTAT[C/T]GAGATGTGCCATTAG | 51666 |
rs139621935 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478081 | GTAAAAAGAACGTTA[C/T]AGAGGACAGTCCAAT | 51666 |
rs139720431 | snp | C/T | 0.00795532 | 0.062565 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540274 | CTCTTTTTCCTAACC[C/T]CGCTTTGACTTTTCA | 51666 |
rs139752723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536162 | TGGAATACTCAAAGG[C/T]GTGAGACTTCTGAAA | 51666 |
rs139856800 | snp | A/G | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 7:95483042 | GACTTGTTCTTCATC[A/G]TCCTTGTCAGCCGAC | 51666 |
rs139910702 | snp | C/T | 0.00358779 | 0.0422022 | | | GRCh38.p7 | 7:95466756 | GCTGGGGAGGCCTCA[C/T]AATCATGGCAGAAGA | 51666 |
rs139923171 | snp | C/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95478828 | GTGAGGATTGTTGAA[C/G]AGATTTTATGTTAAA | 51666 |
rs139944279 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASB4 | GRCh38.p7 | 7:95517719 | CCACTAGTGATCTTC[A/G]TCTGAGCAGTTCCAG | 51666 |
rs139976883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514030 | CACTCCAGGTCAGCT[C/G]TGCACTCACATGATC | 51666 |
rs140027210 | in-del | -/CTCA | 0.00914312 | 0.0669923 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472609 | GAAAAGCAGTCTACT[-/CTCA]CTAATAGGGGTTTTA | 51666 |
rs140055654 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASB4 | GRCh38.p7 | 7:95526717 | AGAATGTTTCACATG[A/G]TTAAGTGCTTAATAA | 51666 |
rs140155447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95494090 | ACAGTGGTCCTTTAG[A/G]ACATTTCACATGGGT | 51666 |
rs140190777 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95533696 | CCATTTCCTAGCTAA[A/G]AGACCCAGAGGTTAA | 51666 |
rs140219037 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485450 | GAAAACCTCCTGTTT[A/G]TCTTCAGATATGTAT | 51666 |
rs140251744 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481253 | ATTTTCCATTATAGG[A/G]ACCAATAAATCTTTA | 51666 |
rs140419892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499540 | TATCACTGACAAAAA[C/T]AGTTTTGGTGAAACA | 51666 |
rs140462942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514688 | TCAGTGATGAAGATG[G/T]TACAAAGAAGCGCAA | 51666 |
rs140475842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503764 | GAAGAACCAATGCCA[C/T]GGCAACTGAAAACCG | 51666 |
rs140481235 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462819 | CAAATTGAGCTATTG[A/G]ATTGAGCTGCTTGTG | 51666 |
rs140527625 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499865 | TACGGGATACATCCT[-/C]TTTTTTTTTTTTTTT | 51666 |
rs140701495 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495739 | AAACTTTCCTTTTCC[-/TT]TTTTTTTTTTTTTTC | 51666 |
rs140738985 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95526598 | ATTATTAACCTCTCT[A/G]AGTACAAATTTCTTC | 51666 |
rs140773630 | snp | A/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485694 | AATAATTGTGACATT[A/T]CATGCCTGGAAATGT | 51666 |
rs140805293 | snp | G/T | 0.000288334 | 0.0120035 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537578 | CTTTTCAGAAATACT[G/T]GGATTTTTACCACTC | 51666 |
rs140821242 | in-del | -/AT | 0.153332 | 0.230554 | intron-variant | ASB4 | GRCh38.p7 | 7:95504355 | ACACAAGTCAACCAC[-/AT]GTTAGGAAATTCCCT | 51666 |
rs140837718 | snp | A/T | 1.64963e-05 | 0.00287192 | missense | ASB4 | GRCh38.p7 | 7:95528211 | TACGTGCTGAAGGTC[A/T]CCTCCGTGCGCCCTG | 51666 |
rs140950721 | snp | C/T | 0.0178098 | 0.0926698 | | | GRCh38.p7 | 7:95468423 | AAAAAGTATGTAAAA[C/T]CACTGAACAGAAGAC | 51666 |
rs141051578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511775 | CTATCCTATGAGGTT[A/C]AGATTTGCAGATTAA | 51666 |
rs141059643 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474736 | CACCATGTTGTCTAG[A/G]CTGGTCATGAACTCT | 51666 |
rs141092941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527357 | TAGGTTTATCTGCTA[C/T]GAAAGAGAAGAAAAG | 51666 |
rs141112072 | snp | C/T | 6.60677e-05 | 0.00574713 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527865 | GGAGACGCCCTTGCA[C/T]ACGGCTGCCCACTTC | 51666 |
rs141143935 | in-del | -/CA/CAGAT | 0.0667028 | 0.170006 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484125 | TAAACTTAGGAGTCG[-/CA/CAGAT]GAGATCAGCCGGGGG | 51666 |
rs141159945 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASB4 | GRCh38.p7 | 7:95516595 | GCTTCAGGAGACAGG[A/G]GAAATAGTTTGTGAT | 51666 |
rs141186023 | snp | A/G | 0.0002638 | 0.0114817 | missense | ASB4 | GRCh38.p7 | 7:95495956 | AGATCCTCTGTGATC[A/G]TGGGGCAAAGCTCAA | 51666 |
rs141239607 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ASB4 | GRCh38.p7 | 7:95496515 | AATGTATAAAGTCTT[A/C]TCTAAGGATATTATG | 51666 |
rs141254016 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505388 | TTAAGGGGCCTAGAA[A/G]ATATATTTAGCAAAA | 51666 |
rs141304082 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95490813 | TAAATTAAACACACA[C/T]GCGCACGCGTGCACA | 51666 |
rs141435603 | snp | A/C | 0.0123036 | 0.0774623 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538669 | TTTAAGGTTTTTTCT[A/C]GATAGTGTGTCTTTT | 51666 |
rs141488591 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539766 | GGTGAGGGATAAAAG[A/T]CTACATATTGGGTAC | 51666 |
rs141602923 | in-del | -/TTTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515146 | GTCCAAGCAATTGTT[-/TTTC]TTTCTTTCTTTCTCT | 51666 |
rs141630664 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475753 | TATAAAACCAAATCA[C/T]GTATTCCAGTGTCAT | 51666 |
rs141647897 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470525 | TTGTAGACAGGGCCA[C/T]TTTGATAAATCTTGT | 51666 |
rs141658798 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474233 | CATTCAGTTTAATAA[C/T]TGTCTCTGCCATTTT | 51666 |
rs141671494 | in-del | -/TGTGTGTGTGTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493381 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTA]TGTGTGTGTGTGTGT | 51666 |
rs141701529 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528670 | CTGATCTAAAGATGA[C/T]TCAGCCTGCTTTGAA | 51666 |
rs141701654 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471563 | AAGGCTCTTCCAACA[C/T]TGTCAGTGTACTTCT | 51666 |
rs141724440 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469313 | CTCAGATGAGGAAAC[C/T]GAAGGCCTGAGGAGG | 51666 |
rs141742617 | snp | A/G | | | | | GRCh38.p7 | 7:95476459 | ATTCACCTATGAGAA[A/G]TCAAGAAATGGAAGG | 51666 |
rs141769326 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95524843 | GATGGAGCTATGGAA[G/T]TTCCTGCCGTTTGCA | 51666 |
rs141774184 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASB4 | GRCh38.p7 | 7:95529651 | TTTTTAAAAAATTAT[A/G]TGTAAAGCCCAGAAT | 51666 |
rs141786563 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95521416 | AAACACTAAGAAGTT[G/T]GAGAGTATCAAATGT | 51666 |
rs141853071 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASB4 | GRCh38.p7 | 7:95515827 | TCCAGAGATGGGCAC[C/T]ATCACCCTTGCTTTT | 51666 |
rs142138079 | snp | A/G | 0.000153988 | 0.00877328 | missense | ASB4 | GRCh38.p7 | 7:95495796 | TTGAAGTCTTCCTGG[A/G]CCACAGGCCTCCATC | 51666 |
rs142204124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498275 | TAGGAGTTTGAGTTC[A/G]GCGTGGGCAACATCA | 51666 |
rs142269439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95492675 | GATCATTTTTCTTCC[C/T]ATTGCAGAAGCAGGC | 51666 |
rs142282671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473511 | GCAGCTGCTAGACCT[C/T]GTACTGTTTGTCCTT | 51666 |
rs142415919 | snp | C/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95480146 | ACACCTTGTTCTGAT[C/G]TATACAAGGGTGGCT | 51666 |
rs142420362 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520250 | CTTTAAGGAAGTTAC[A/G]GACAAAGGGAGCAGA | 51666 |
rs142449628 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASB4 | GRCh38.p7 | 7:95532510 | GAGGAAAAGGTAACA[C/T]GAGGGTCTGGGAGAG | 51666 |
rs142454952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523796 | TTACTCTAAGGAGTA[A/T]GTAGTTATTTTAAAT | 51666 |
rs142518207 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASB4 | GRCh38.p7 | 7:95517143 | GGTTATTTGGCTTTT[C/T]CTATTGAGTTGTAAT | 51666 |
rs142544480 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95537214 | TTAAAAGTCACCTAA[A/C]TTGAGTGAGCTGCAT | 51666 |
rs142632339 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469736 | TGTTGGTTCATTGCT[C/T]GTTCATAAAAAATAA | 51666 |
rs142673105 | snp | A/G | 0.0158469 | 0.0875917 | | | GRCh38.p7 | 7:95464511 | CATCGCCCATATTTT[A/G]TAATTATTAATTAGC | 51666 |
rs142708535 | snp | C/T | 0.00716266 | 0.059414 | | | GRCh38.p7 | 7:95461028 | TGGAGGATGTCCAGG[C/T]AGAGGTGTGCTGCAG | 51666 |
rs142733506 | snp | C/T | 0.00993419 | 0.0697739 | | | GRCh38.p7 | 7:95467514 | GACAGAGATCACAAG[C/T]CCTCAGAAACATTGT | 51666 |
rs142735600 | snp | A/G | 0.000148858 | 0.00862593 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537611 | TCTTTACTGTGTGCT[A/G]TAACTCTCCAAGGAC | 51666 |
rs142799070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95518780 | ACAATTTGACCCAGA[A/G]GGTTTAGAATTGTAA | 51666 |
rs142827039 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487984 | CTACTCTGTTTAATA[C/T]GCACATGGGCACAAG | 51666 |
rs142852084 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500032 | TCATTTTTAAGAAGC[A/G]GGACAAAGTAAAAGA | 51666 |
rs142852535 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513253 | TTTTGTTTTTTGTTT[-/G]TTTTTTTTTTTTTTT | 51666 |
rs142912145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493732 | CACTATAACCAGTTT[C/T]GTGTTCTCAGTGTTT | 51666 |
rs142926039 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95527064 | CATAAATAAAACATT[A/T]TGCAGTCTCTGAATC | 51666 |
rs142959063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535012 | CCCTGACTCCATCCA[A/G]GTTGGCCTCTTTACT | 51666 |
rs143019035 | in-del | -/T | 0.0868034 | 0.189386 | intron-variant | ASB4 | GRCh38.p7 | 7:95486188 | GTGTTATTGTAGAAC[-/T]GTTAGAAAATGATTT | 51666 |
rs143033531 | in-del | -/TTTG | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472387 | CAAATCTCAATAATA[-/TTTG]AACATTTTGCACTGG | 51666 |
rs143072407 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502132 | GAGAGAGAAAGAGGT[-/A]AAAAAAAGAAAAAGA | 51666 |
rs143137606 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481826 | CATACTATTTCAAGA[A/G]CAAAGGACACTGTTC | 51666 |
rs143166503 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95498806 | GGTGTAGGATTCATT[C/T]TGAGTTAATTTTTTT | 51666 |
rs143171764 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASB4 | GRCh38.p7 | 7:95534699 | GTCTTTTATTATTTA[C/T]TGACTTATATTGCTC | 51666 |
rs143176022 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95533505 | ACCCAACTCCCAGTG[A/G]CTTGACCTTCTAATT | 51666 |
rs143245288 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464268 | CATAGCCTGCACCAT[C/T]AGGTGAAGTTTAATT | 51666 |
rs143313098 | snp | A/C | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95463916 | ATCATTTTGCCACTG[A/C]AATGAACATGGACAG | 51666 |
rs143393596 | snp | A/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 7:95466761 | GGAGGCCTCACAATC[A/G]TGGCAGAAGACAAAG | 51666 |
rs143418378 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469737 | GTTGGTTCATTGCTC[A/G]TTCATAAAAAATAAA | 51666 |
rs143440362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95507875 | AGTTAAACAGCTGCT[A/G]TTGGATTTAGTGACA | 51666 |
rs143452090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523660 | ATGTTTCAGCTTAAT[A/C]ATTCTATTTTGGGGG | 51666 |
rs143461634 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462437 | CCTATTTATATTTTA[G/T]CAGGATTTCCCCCCC | 51666 |
rs143546171 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528693 | GCTTTGAAATTAGCT[C/T]GTAGCCATGAAAGGG | 51666 |
rs143546324 | in-del | -/TG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491654 | TGGTGGTTATATTTT[-/TG]GGGGGACAAATTCTG | 51666 |
rs143626722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95504931 | CAGTTACTCCAGTCC[C/T]GTAAAGCATGTTCCA | 51666 |
rs143736047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95511636 | CATTGCACTCCAGCC[C/T]GGGCAACAAGAGCAA | 51666 |
rs143786307 | in-del | -/GT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527173 | TTGGTGACTAAAGTC[-/GT]GTGTGTGTGTGCATG | 51666 |
rs143829781 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95523631 | TATTAATAAAGACTC[-/TT]AACATAGTTCAAATG | 51666 |
rs143880845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494103 | AGGACATTTCACATG[G/T]GTGTTTATGCTTATA | 51666 |
rs143945812 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95489884 | GTTTTCACTGGTTAC[G/T]TCCATACTGGAAAGA | 51666 |
rs143968145 | snp | G/T | 0.0138799 | 0.0821421 | | | GRCh38.p7 | 7:95466553 | AAATACTATGGTTGT[G/T]CAAAGGAAGACATTT | 51666 |
rs144123084 | in-del | -/TCTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515415 | CTTTTCTTTTTCCTT[-/TCTC]TCTCTCTTTTTTTTT | 51666 |
rs144160590 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant | ASB4 | GRCh38.p7 | 7:95521885 | GAACAGTAGTTACCT[-/C]TGTGGAGGAAAAAAT | 51666 |
rs144162427 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | ASB4 | GRCh38.p7 | 7:95527557 | CAGCAACGCTCCAGC[-/T]ATTCTGGCACAAATC | 51666 |
rs144179096 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472510 | TATCTCCCTGTGATT[A/C]CTGTGGAACTGCAGT | 51666 |
rs144195385 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513249 | TTTTTTTTGTTTTTT[G/T]TTTGTTTTTTTTTTT | 51666 |
rs144231000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95526532 | TACCACCTGTGACAC[C/T]GGCCCCAGCTAGTTG | 51666 |
rs144260745 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539249 | TTGAATAGAGATGAT[A/G]TCAGATATTCCAATA | 51666 |
rs144422348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489424 | GTTCAAACTGTGGAT[C/G]CTGTCTTTCTCCAGC | 51666 |
rs144489049 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485077 | ATATGTATATACACA[C/T]ACACACACATCTATT | 51666 |
rs144489190 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540307 | AATGACACTGAAGAA[C/T]TCTACACATTTCATT | 51666 |
rs144514403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95513358 | GGAATGGAATGATTT[A/G]TTTTAAGGAATTGGC | 51666 |
rs144557548 | snp | A/G | 0.000710816 | 0.0188389 | intron-variant | ASB4 | GRCh38.p7 | 7:95536393 | CAGAATGAATGAACC[A/G]TATATGTGCATCAAA | 51666 |
rs144625229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518286 | AAAAGAAATAAGAGT[A/G]GCTTCCAGGCTTAGA | 51666 |
rs144643453 | snp | A/C/T | 0.000121475 | 0.00779256 | intron-variant, missense | ASB4 | GRCh38.p7 | 7:95528353 | AGATTCAAATGGCAG[A/C/T]CTTGTCTGAAATCTC | 51666 |
rs144658082 | snp | C/T | 9.89218e-05 | 0.00703215 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528075 | CAATGCCCGAGATGA[C/T]GACTTTAAATCTCCC | 51666 |
rs144703539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95526658 | CCACTGCAAAGGATT[A/G]CTTGGAAGGTTCAAT | 51666 |
rs144704402 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95524006 | CCAATGTTGATAAGG[A/G]TGTAATACAATGAGA | 51666 |
rs144716203 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95493595 | GTTAAAAAGCAATAC[A/G]TGCACAGGATACTAA | 51666 |
rs144766576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520370 | TCTGTCTACAAACTC[A/G]GGTTTATTGGAAAGT | 51666 |
rs144825222 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95501332 | GACTGTTCCCTGCTA[C/T]TTTATCTGACAGTGA | 51666 |
rs144892508 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95489939 | TCCAAAGGCTTTACC[A/G]ACTTGATCTTCCTTC | 51666 |
rs144911163 | snp | A/G | 8.23947e-05 | 0.00641799 | missense | ASB4 | GRCh38.p7 | 7:95486101 | CAAAGGCAAATAGAT[A/G]TGGACACTGTTTTTG | 51666 |
rs144991672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511009 | GAAATGCAAGTGTTT[C/T]CTTTGTCATCTCTGT | 51666 |
rs144996263 | in-del | -/TA | 0.288906 | 0.246954 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485057 | ATATGTGTATATATG[-/TA]TATATATGTATATAC | 51666 |
rs145070794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95500170 | GGAGAGCAGAAAGCA[C/T]AGACATTTTCATAAG | 51666 |
rs145180623 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ASB4 | GRCh38.p7 | 7:95496644 | TTGAGCCCAGGAGTT[C/T]GAGACCAGTCTCGGC | 51666 |
rs145225342 | snp | A/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95463131 | CTCACTGGAACCTTG[A/G]ACTCCTGGGCTCAAG | 51666 |
rs145243211 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485511 | CAAAATTATTACAGG[A/T]TTTTAGAAGCAAATG | 51666 |
rs145261733 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASB4 | GRCh38.p7 | 7:95515090 | TCTTGTTTCTTCAAG[G/T]TACTCCTTCCTCATA | 51666 |
rs145310473 | snp | C/T | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 7:95481270 | CCAATAAATCTTTAC[C/T]GGTTCAGTTCCAGTT | 51666 |
rs145347232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531992 | GGCTACTGGTAGATG[G/T]CTGGTATTACAAACA | 51666 |
rs145428530 | snp | A/C/T | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95478852 | TGTTAAACACACATG[A/C/T]TCCCAGTATGTAATT | 51666 |
rs145488831 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95496388 | TATATTCTAATAAGG[A/G]AGACAAATATTAACA | 51666 |
rs145594813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95504135 | GCTAAGCAGCATATT[A/G]TTTCTACCTATTCCA | 51666 |
rs145639868 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462848 | TGAGAAATTAGACAG[C/T]TATTGATTTGGGAAC | 51666 |
rs145811803 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484627 | ATTCTAAGAATCAAA[C/T]AGTATCATTGTAAGT | 51666 |
rs145919755 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95480748 | GACAAGCCTTTCCCA[C/T]TGTGTCCTGATCCAC | 51666 |
rs145977927 | snp | A/C/T | 1.64969e-05 | 0.00287196 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537634 | CCAAGGACTCTCATG[A/C/T]ACTTATCGAGATGTG | 51666 |
rs145996843 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95517215 | ACTCTGTTGCCCAGG[A/C]TGAGGTGCAGTGGAG | 51666 |
rs146016934 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95514021 | TCTGCATTTCACTCC[A/C]GGTCAGCTGTGCACT | 51666 |
rs146119455 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95493981 | TAGTGTAGTGCATGT[A/T]CTTGTATGTAGACCA | 51666 |
rs146138432 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASB4 | GRCh38.p7 | 7:95489433 | GTGGATCCTGTCTTT[C/G]TCCAGCACCTAATCA | 51666 |
rs146157551 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540324 | CTACACATTTCATTG[A/C]TTTTATCAACAGTTA | 51666 |
rs146164007 | in-del | -/A | 0.0930568 | 0.194599 | | | GRCh38.p7 | 7:95481361 | AATAGCAAAAAAAGG[-/A]AAAAAAAAACAACAA | 51666 |
rs146207329 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515233 | TTTCTTTCTTTCTTT[C/T]TCTTTCTTTCTTTCT | 51666 |
rs146221689 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95476262 | AAATTGTGGTATGCA[A/G]CGGCAAGGCTTCCAG | 51666 |
rs146240126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471596 | GACAGTATGTATCTA[A/G]ACTCATTTGGAAATA | 51666 |
rs146251713 | snp | C/T | 0.000110585 | 0.00743506 | intron-variant, stop-lost | ASB4 | GRCh38.p7 | 7:95528373 | TCTGAAATCTCCAAG[C/T]AACTCAAGCTTGCTT | 51666 |
rs146258725 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466849 | TCTCTTTATAAAACT[A/C]TCAGATATTGTGAGA | 51666 |
rs146363240 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540053 | GGAGAAGATGTTCCT[C/T]GCCCAGGGAAATGAA | 51666 |
rs146381486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95535997 | TTCTGTGTCCAGTCT[C/G]TCTCTAAATTGCTTC | 51666 |
rs146416403 | snp | C/T | 3.29837e-05 | 0.00406088 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528153 | GCTGGAAGCTGGCGC[C/T]GAAGCCAATCTCATG | 51666 |
rs146522808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509769 | TGGCTATGTCAGGTA[C/G]TTGAAAATAAAATGT | 51666 |
rs146639524 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485273 | ACTGTCTTTTCTAGC[C/T]GATTAAAAAACAGGA | 51666 |
rs146658149 | snp | A/G | 0.000441108 | 0.0148445 | intron-variant | ASB4 | GRCh38.p7 | 7:95536561 | TGGAGGTAAATAATC[A/G]ATTCCCTTCTAATAG | 51666 |
rs146658609 | snp | G/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95480827 | ATTTTGAGGTTATTT[G/T]CTATGCAGCAAAAGA | 51666 |
rs146677487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533557 | GTCTTCATCTCTTGA[A/T]CTTCATGACCCCCTT | 51666 |
rs146716091 | snp | C/T | 5.10512e-05 | 0.00505203 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95485977 | GAGAGGAAGGATGGA[C/T]GGCACCACTGCCCCT | 51666 |
rs146766559 | snp | A/G | 0.0513262 | 0.151752 | | | GRCh38.p7 | 7:95462455 | GGATTTCCCCCCCTC[A/G]TATTTACTTCCTTTA | 51666 |
rs146786435 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95514197 | CCCTCTCTTAACGTC[A/T]TTTCTTTCTCTACTC | 51666 |
rs146804728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511029 | GTCATCTCTGTAAGT[A/G]ATAACTTATGGAACA | 51666 |
rs146896450 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95511843 | CAGGTTTTGACTGCA[C/G]TGACCTCAATACAGA | 51666 |
rs146984848 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ASB4 | GRCh38.p7 | 7:95490815 | AATTAAACACACACG[C/T]GCACGCGTGCACACA | 51666 |
rs147001148 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASB4 | GRCh38.p7 | 7:95488157 | CCATCCTGCCTAACA[C/T]GGTGAAACCCCATTT | 51666 |
rs147018199 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538688 | AGTGTGTCTTTTTGG[C/T]ATGGTTTCTTGGTTA | 51666 |
rs147089809 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469514 | ATGTGAACAGGAATG[A/T]GAAAATTTTCCATTT | 51666 |
rs147091900 | snp | C/T | 0.0019929 | 0.0315036 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495981 | GCTCAATTGCTACTC[C/T]TTAAGTGGACACACA | 51666 |
rs147104656 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464460 | ATGATGCTTGAAAAC[A/T]ACAAATGCAAATAGT | 51666 |
rs147105797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521596 | AAAGATATTTACTAT[A/T]GGGAAAAAGCTAAAA | 51666 |
rs147121041 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95515982 | CTGTTTCACTCCAGT[A/C]CTGCCTCCATGAGCC | 51666 |
rs147136982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512067 | CTTGCTCCCAGCCCC[G/T]GATGAAGGGGAAGCA | 51666 |
rs147153438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95508216 | TGAGATCCAGAGCAG[A/G]TAAAAGGATTGACTT | 51666 |
rs147242780 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ASB4 | GRCh38.p7 | 7:95488254 | GCTGAGACAGGAGAA[C/T]GGTGTGAACCCGGGA | 51666 |
rs147264619 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483900 | GTGTGTCACAGAGAG[G/T]CAGTTGGGAGCCAAT | 51666 |
rs147332526 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495635 | AAACCTCTGTCATCC[C/T]CTCTCCACCCCACTT | 51666 |
rs147334719 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95506903 | TTGGATATCGAACCT[C/G]CCTGGACTGTTTCTC | 51666 |
rs147439121 | snp | C/G/T | 0.00199529 | 0.0315338 | | | GRCh38.p7 | 7:95483041 | TGACTTGTTCTTCAT[C/G/T]GTCCTTGTCAGCCGA | 51666 |
rs147455316 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478331 | AAACTGTGCTGGACG[A/G]CGTGTAAATGCAGGT | 51666 |
rs147455627 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASB4 | GRCh38.p7 | 7:95535084 | CACATGCACACACAT[C/G]CGCACACTCTTACTT | 51666 |
rs147471704 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95530940 | ACTTTGGGGTCAAAC[C/T]TGGATTCTGTCACTT | 51666 |
rs147543022 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95459625 | ACGATGCTCTGCCCA[C/T]TGGTTCTGCCACTGC | 51666 |
rs147592802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503347 | GAAACTAAAAGACTG[C/T]GAGCATCTTGTTTTC | 51666 |
rs147702846 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479123 | GCTGAGGAGTGTGTC[C/T]AGTAGGTCTCATTTT | 51666 |
rs147719163 | snp | G/T | 0.00279162 | 0.0372561 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474614 | GCAGCCTTAACCTCC[G/T]GGGCTCAAGCAATCC | 51666 |
rs147762255 | snp | A/G | 1.65562e-05 | 0.00287712 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537729 | ATTGAAAAAGTACTT[A/G]CTTTTAGAGCCAGAG | 51666 |
rs147798502 | snp | A/G | 4.94727e-05 | 0.00497332 | missense | ASB4 | GRCh38.p7 | 7:95495856 | CTTCTGGTGCTACTG[A/G]ACCACAATGCTACAA | 51666 |
rs147849880 | in-del | -/C | 0.0271762 | 0.113356 | intron-variant | ASB4 | GRCh38.p7 | 7:95512110 | TCTGTAACACTTGAT[-/C]CCTCCCATGCTGTAG | 51666 |
rs147861015 | in-del | -/AAT | 0.316968 | 0.240864 | intron-variant | ASB4 | GRCh38.p7 | 7:95522401 | ACATGGGCTTAAGCA[-/AAT]AATATTTCATTATAT | 51666 |
rs147891671 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474174 | TGACTTCAAATTAGC[A/G]AATATGCATATGTGC | 51666 |
rs147908060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95526686 | AATGAGGCAATATAT[A/G]AAAAGCATTTAGCCC | 51666 |
rs147923767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520613 | TTGCTTTTAATTTAT[C/T]TGAAATTAAACACAC | 51666 |
rs147976085 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469918 | GAAGGCATTATGATG[C/T]ATGAATTTTTAAATA | 51666 |
rs147992028 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95523682 | TTTTGGGGGAATTTA[A/T]TCCAAGGAAATAATC | 51666 |
rs148045679 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASB4 | GRCh38.p7 | 7:95529423 | TTACCTGGGTAAAAT[A/G]TCAGGGACTTGTCTG | 51666 |
rs148258153 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482693 | CAATAGGCTTGCTGA[C/T]GTAGGGAGAAAAAGA | 51666 |
rs148278044 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95498987 | TCTGGACTCCAGCCT[A/G]TTCCATTGACCTATA | 51666 |
rs148326882 | snp | G/T | 0.0130921 | 0.0798413 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539523 | TTCAAAAAATAGTTT[G/T]CTTGCAGCAAGTGGT | 51666 |
rs148430563 | snp | A/G | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 7:95461394 | ACGTTAAGATTTAAC[A/G]ACTGCCCTATTGGAT | 51666 |
rs148446938 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASB4 | GRCh38.p7 | 7:95513448 | TAGGGAATAGATACA[A/G]TCTGTTGCCAGAGCC | 51666 |
rs148500378 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95518435 | GAAATCAAATGGAGG[A/G/T]CCTTGATTCTGAATT | 51666 |
rs148543987 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95497112 | TTAGATCCTACAGGG[-/C]CTTTGAGGGTCAAAG | 51666 |
rs148552388 | in-del | -/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473641 | TTTTTTTTTTTTTTT[-/T]AATCAACGGAATAAT | 51666 |
rs148566955 | snp | A/G | 0.0244538 | 0.107838 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484972 | TATATATATGTGTGT[A/G]TATATGTATATATGT | 51666 |
rs148586705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501550 | CAAATTTCCAGTAAA[C/T]AATGCAGTGTTACTA | 51666 |
rs148639746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508266 | TCTATCGTAGCCAGA[C/G]GCAGAGAAGGAGAGA | 51666 |
rs148706073 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515316 | CTTTCTTTCTTTCTT[C/T]CTTCCTTCCTTCCTT | 51666 |
rs148707477 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472543 | TATAAATCTGCAGTT[C/G]CCTGTTAGTGGATTT | 51666 |
rs148761257 | snp | C/T | 0.00557542 | 0.0525036 | | | GRCh38.p7 | 7:95479256 | GGTCTTTCACCATAA[C/T]ACCACTTAGTATTTC | 51666 |
rs148812162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523312 | CAAACTGGTTACAAC[A/G]TTTATAGCAATTATG | 51666 |
rs148823603 | snp | A/C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521765 | GTGAGATACAATGTA[A/C/T]GTAGTTTTTTAAAAC | 51666 |
rs148832527 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95537149 | CACTGGGCTTGGAGG[A/T]CTGTGGCTTAGGTGT | 51666 |
rs148880252 | in-del | -/AAAA | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95465959 | AACAAACAAACAAAC[-/AAAA]AGACAACTGAATGCA | 51666 |
rs148900076 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95504478 | CCACCTCACCGCGTT[C/G]CATCTTTTCATCTTC | 51666 |
rs149025895 | snp | A/C | 0.120326 | 0.21374 | | | GRCh38.p7 | 7:95475535 | ACTACAGGTGCGTGC[A/C]ACCACACCTGGCTAA | 51666 |
rs149041181 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95490067 | TTTATTAATCAGGGT[A/G]ATGCACTTTAAGTAC | 51666 |
rs149089341 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASB4 | GRCh38.p7 | 7:95534328 | AGCCTGGGCTAAAAA[C/T]GTAAAACTCCATTAA | 51666 |
rs149137628 | in-del | -/C | 0.0460142 | 0.144533 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540071 | CCAGGGAAATGAAAA[-/C]TTTTCTTATTCACCT | 51666 |
rs149162142 | snp | C/T | 0.0146672 | 0.084371 | | | GRCh38.p7 | 7:95463759 | TCTCAGGTATTTCTT[C/T]ATAGCAGTGTGGGAA | 51666 |
rs149340528 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478203 | CTGCCTGGAGTACAA[C/T]TGTGAGGTAAATGTT | 51666 |
rs149352133 | snp | A/G | 9.89609e-05 | 0.00703354 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528003 | CTTTAAGGAGCAGGA[A/G]TACAGCACGGAGCAC | 51666 |
rs149354545 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493328 | GAAAGCAAGATGGCT[C/G]TAGAATTCTGAATGG | 51666 |
rs149398589 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515235 | TCTTTCTTTCTTTTT[C/T]TTTCTTTCTTTCTTT | 51666 |
rs149408917 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ASB4 | GRCh38.p7 | 7:95500471 | CTCGAAAGGCTGAGG[C/G]AGGAGAATTGCTTGA | 51666 |
rs149483390 | snp | C/G | 0.00557542 | 0.0525036 | | | GRCh38.p7 | 7:95466355 | GTGCGTGATCACTGT[C/G]TAGGGAATGGGTACA | 51666 |
rs149492426 | in-del | -/TGTGTGTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493385 | GTGTGTGTGTGTGTG[-/TGTGTGTA]TGTGTGTGTGTGTGT | 51666 |
rs149497230 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481710 | TGTACACAGACAAGC[A/G]TCTGGGACTTTGTGC | 51666 |
rs149567185 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539154 | AAGCAGAAGTAAATT[A/G]CAAACAAATCTGTCA | 51666 |
rs149634538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506233 | TCTGAAATATTTAAA[C/T]TCAGTGGGTATTTTA | 51666 |
rs149668942 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537721 | CCATTGTCATTGAAA[A/C]AGTACTTGCTTTTAG | 51666 |
rs149672408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95496184 | GCCTAGTACAGAAGG[C/T]CCTAAAAAATACATA | 51666 |
rs149719385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95503976 | TCTACTTAATGCCCC[C/T]ATCTCCTGGCCTTTG | 51666 |
rs149743736 | in-del | -/GATTTATGTTCTCC | 0.207559 | 0.246371 | intron-variant | ASB4 | GRCh38.p7 | 7:95535420 | CCCCTCAGAAAGGTT[-/GATTTATGTTCTCC]GAAGTTTCATGGGAA | 51666 |
rs149793874 | snp | A/G | | | | | GRCh38.p7 | 7:95468615 | CCTGCACTAAGTCAT[A/G]TCTGTCATTTTAAGT | 51666 |
rs149809142 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484273 | AGAGGCAAAGGTTGC[A/G]GTGAGCCCAGATCAC | 51666 |
rs149825565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95535913 | AATCTAAGTTGATTG[A/G]CTAACATTGAATTTT | 51666 |
rs149942720 | in-del | -/G | 0.0681886 | 0.171594 | | | GRCh38.p7 | 7:95481128 | TAAACTAGAAATAAT[-/G]ATAACAATTAAAATT | 51666 |
rs149951991 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95486034 | AGTTAAGAGAAATTT[C/T]CTTGAGGCGCTAAAG | 51666 |
rs149953842 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95509300 | GGAGCAATGGGGAGT[A/C]AGATATATGAAAAAG | 51666 |
rs150000377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514700 | ATGGTACAAAGAAGC[G/T]CAACCTGGAGTCCAT | 51666 |
rs150021121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95531396 | TTCAAAGACTACTTT[C/T]CCTCCAGCGAAAAGG | 51666 |
rs150126950 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASB4 | GRCh38.p7 | 7:95486539 | TACCTGGTTTAAGAA[C/T]ACGCTGCTAATTCTC | 51666 |
rs150174034 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASB4 | GRCh38.p7 | 7:95492690 | CATTGCAGAAGCAGG[C/T]GCAAATTTCCAATCA | 51666 |
rs150266348 | snp | A/C | 0.000153988 | 0.00877328 | missense | ASB4 | GRCh38.p7 | 7:95527880 | CACGGCTGCCCACTT[A/C]GGCCTTTCGGAGCTG | 51666 |
rs150267393 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475166 | ACAAGCCCACCAGAG[A/G]ACTCTGAAGTACCGA | 51666 |
rs150283322 | snp | C/G | 0.000461574 | 0.0151847 | missense | ASB4 | GRCh38.p7 | 7:95528113 | AGGCAGCCTGGAACT[C/G]TGACCACGTGCTCAT | 51666 |
rs150330277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533734 | CAGCCTTTGGTCTTA[A/G]ATCTCTGAAATGGGG | 51666 |
rs150404784 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95499586 | TTTGAATGGTATAAA[C/G]TGCAAATGGGTGGTA | 51666 |
rs150527249 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470660 | GCTGTGGTGTCAGAT[C/T]CTTTCTCATTTCCTG | 51666 |
rs150588244 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537640 | ACTCTCATGCACTTA[C/T]CGAGATGTGCCATTA | 51666 |
rs150597440 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95530193 | GGGCTGGGTGCAGTG[A/G/T]CTCACCCCTGTAATC | 51666 |
rs150650331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95535452 | GTTTCATGGGAAAAA[C/T]GGAACTGATACGAAA | 51666 |
rs150716774 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ASB4 | GRCh38.p7 | 7:95501724 | CTAGAGGTGTCACCT[G/T]TCCCAGCCGGTACAG | 51666 |
rs150721716 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464846 | TGGAAGACATTTTTA[C/T]GTTACCAATCTTGAC | 51666 |
rs150738349 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95516907 | CAAATGTCATCAAAT[C/G]GTGTTCACTTTCAGC | 51666 |
rs150785491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95525527 | GAAAAGGAAACCATG[C/T]AGCATATCTAGTTGC | 51666 |
rs150813202 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510127 | TTCTTAAAAAAAAAA[-/A]TGAGAAGGCAGCTGG | 51666 |
rs150860266 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95489103 | AGTCCATCTAAGCCT[A/G]TATGAAAGTCAGTGT | 51666 |
rs150914749 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95494876 | AAAACCAATGGGAAA[A/C]ATTATTGAAGATCTC | 51666 |
rs150946272 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485583 | TGTCAGAGCAAGACG[C/T]TGGATCTCCAGCCAG | 51666 |
rs150962920 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537335 | AGGCACTTCACACTT[A/G]CATATTTTATCTTAT | 51666 |
rs150981704 | snp | A/T | 0.0517044 | 0.152246 | | | GRCh38.p7 | 7:95462008 | CGTGCCATGTGGAAC[A/T]GTTAGTCAATTGACC | 51666 |
rs151035411 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95467813 | CTCTGCACAACCTTA[C/G]GGTCACCATTCACAT | 51666 |
rs180848717 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASB4 | GRCh38.p7 | 7:95488754 | AAGTGCATAAATAAG[C/T]GTGCAGCTTGATTAC | 51666 |
rs180850470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95529728 | ATGAGGAATAGAATA[A/G]GAATAATGTTACAGT | 51666 |
rs180868831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507817 | CAGGAAGGAGGGAGA[A/C]GTCAGAAGTGTTAAA | 51666 |
rs180941656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95501459 | GGCCTGCTGGACAGA[C/T]GCTGCTCTTACCACC | 51666 |
rs180957075 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ASB4 | GRCh38.p7 | 7:95523748 | TAATTTTAAGATCAA[A/C]ATTTTGGAAAAAATC | 51666 |
rs180960300 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462646 | AAGGCTTACATAACA[A/T]GGAACTCATTTAACA | 51666 |
rs180966642 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484720 | ACGACATATAAAAAT[A/G]CAATTTATTTGCATT | 51666 |
rs181025268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95511898 | TGCTGCCTTCCCTTT[A/G]CTACTTTAGAGTCCT | 51666 |
rs181034272 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492968 | ACTCAATAGAAATGT[A/G]TAAATGAATCTATAT | 51666 |
rs181034573 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474590 | GCAGTGGTGCAATCA[C/T]GGCTCACTGCAGCCT | 51666 |
rs181067769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507251 | TGGTCAGATTCTCCG[A/C]AAAAAAATCTAACTG | 51666 |
rs181081697 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529290 | CTTAGGTTTCCCCCT[C/T]GCTCTAAAAATTTAA | 51666 |
rs181087048 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468948 | TTGAACATGTTGTAC[A/G]ATCATACTTTCCATT | 51666 |
rs181092607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95487794 | TGGCTTTCAATTAGG[A/G]AGATAGCAAATTACA | 51666 |
rs181115415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95519224 | AAAATATGCTTTGGC[A/G]ACAGTTCATGACATA | 51666 |
rs181133384 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538798 | AAAATGGGGGAAAGA[A/C]AGTGTGTGAGGGGAC | 51666 |
rs181139421 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95480477 | GATATGATAGAAACA[A/G]TGGTATATGACTTCC | 51666 |
rs181205120 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484338 | CCTGTCTCAAAAAAA[A/G]ATAACAAACAAAACT | 51666 |
rs181220543 | snp | A/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95462013 | CATGTGGAACTGTTA[A/G]TCAATTGACCCTCTT | 51666 |
rs181556830 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95535128 | GATCATAACCTTTCT[G/T]TCTCTGTTTTATCTG | 51666 |
rs181591125 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513264 | GTTTGTTTTTTTTTT[G/T]TTTTTTTTTTAGAAA | 51666 |
rs181668378 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95529781 | AATAGGTTTTATACA[G/T]ACTATTTCATTTTAT | 51666 |
rs181682873 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538171 | AGGCTTTGCAATTGG[C/T]CTCTTAAACTTGGTG | 51666 |
rs181695422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489282 | AGACAGAATAAAGCT[A/G]TTGGATTACAAATAA | 51666 |
rs181695597 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95508638 | CACTCAGCTGCTTGG[C/G]TGCAGGCACTGAGAC | 51666 |
rs181706307 | snp | C/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470824 | GGGTTTTCTTTTTTC[C/T]CCCCATTAGGAAAGA | 51666 |
rs181708204 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95523266 | GAAAACTTGACAATC[A/G]AAAGTCAACATCACT | 51666 |
rs181720426 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95494209 | CCCACTTTTAATGTG[C/G]TCATCATCCTCAGAG | 51666 |
rs181795401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95534790 | ACAAAAAACAGGTCA[C/T]AAATCTCCCAGAATT | 51666 |
rs181810645 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95493866 | AACTGCCCCTTTTTT[A/T]AATGGTTGTATAGTA | 51666 |
rs181821599 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474806 | GGAATTATGGCATGA[A/G]CCACCATGCCTCATC | 51666 |
rs181822807 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95512519 | GAATTCCTTGGAAAA[A/C]TAAGTCCTGGAAAAT | 51666 |
rs181842002 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517832 | CCCTTTCAAGGAGTT[C/T]AAACAAAAAGCAATA | 51666 |
rs181864158 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501030 | GTTTTTATCTTTATT[C/G]ATTTTTAAATTTAAT | 51666 |
rs181866084 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480134 | GTCCACAGGAGCACA[A/C]CTTGTTCTGATCTAT | 51666 |
rs181875826 | snp | A/G | 0.00557542 | 0.0525036 | | | GRCh38.p7 | 7:95475479 | ACCTCCACTTCCCAG[A/G]TTCAAGCAATTCTCC | 51666 |
rs181937682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503212 | TTTTTTTTAAAGTGT[A/G]GCAGCTGGCAGATAT | 51666 |
rs182124826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497015 | TAGAAGAGGGCTACT[A/G]TGACCAGAGTATCAT | 51666 |
rs182164773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95520891 | GGTGGGGTAAGTACC[C/T]CTTATTCACTGTCTT | 51666 |
rs182171539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498465 | GTTGAACATGTTTTC[A/C]TGTATTGATTTGCCA | 51666 |
rs182175247 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538947 | TTGAAAATGGTAAAA[A/G]TTTGAGAAACTTGGG | 51666 |
rs182189008 | snp | A/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 7:95481027 | GAGTGTCAAGATCTA[A/G]GCTTGAGTGTTATAT | 51666 |
rs182232687 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524317 | ATGAGAACTAAACAG[A/C]ACAAGACAGATTATT | 51666 |
rs182344673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95525565 | GGTCAAAGATCAATC[A/G]TAAATGTCCAAGTAC | 51666 |
rs182376372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95505126 | GGCACAAAGAGAAGA[A/G]AAAAATACATAATGT | 51666 |
rs182380460 | snp | C/G | 0.000580057 | 0.0170203 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485952 | TAAATCACAACAAAG[C/G]TTCCAGAGGGAGAGG | 51666 |
rs182404249 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470444 | AAAAAAACTCTTAAT[A/C]CATAGATCTAAGCAA | 51666 |
rs182493778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499904 | TTTGAGACGGAGTCT[C/T]GCTTTGTCGCCTGGG | 51666 |
rs182498265 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95531284 | CTACATCTTGCTAAG[C/G]GCTGGTCATTCTTCA | 51666 |
rs182502180 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95530380 | TGAGGCAGGAGAATG[A/G]CTTGAACCCGGGAGG | 51666 |
rs182511759 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95482619 | CGCCTGAAGGACTCA[C/T]GTCATAGGGTTTCTT | 51666 |
rs182526692 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460767 | TAATCACCAAGACAA[A/T]GGGGAAAATGTCTCC | 51666 |
rs182530503 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509074 | GAGATTGGGTGGGTC[A/T]TTCATGTGGTATTAA | 51666 |
rs182531062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491118 | AAGTTCAGATTCTGG[A/C]ATGCAGATAATTAAT | 51666 |
rs182654296 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513944 | CGAAGGATTTCGATG[C/T]TGGCATAAATTACCA | 51666 |
rs182695316 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95476186 | ATCCTACACATCTGT[C/T]GGTCCCTACTACACC | 51666 |
rs182766607 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ASB4 | GRCh38.p7 | 7:95510857 | GAAATTGAAGGATGA[A/T]GTTTCCTTAGGCCTG | 51666 |
rs182814243 | snp | A/T | | | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471138 | TTTCTAATGTCCATA[A/T]CCTGCACAATTGCCA | 51666 |
rs182833141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536828 | CTCATTAATTTAGAT[A/G]AGTTAAATGATAACA | 51666 |
rs182907832 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515312 | CTTTCTTTCTTTCTT[C/T]CTTTCTTCCTTCCTT | 51666 |
rs182937897 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466581 | TTTTTATCTTACCAC[C/G]CTTAACTTATAAAGA | 51666 |
rs182947834 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95535471 | ACTGATACGAAACTC[A/G]TGATGAACAAATTTA | 51666 |
rs182948533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95532417 | TTTTTTTTCTCCCAG[C/T]GTAATTCAGAAGAAA | 51666 |
rs182964464 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95494404 | TTTGGCAGTACCATC[A/C]CACTGTTGGCTTATT | 51666 |
rs183012450 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485460 | TGTTTGTCTTCAGAT[A/G]TGTATGACAATGGTT | 51666 |
rs183028613 | snp | C/T | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95465727 | GCTGGTCTTGAAATC[C/T]TGTTCTCAAGTGATC | 51666 |
rs183066165 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95514526 | CCAAGAGTTAGAGGA[A/G]GAGGTTGACTGACAT | 51666 |
rs183071589 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ASB4 | GRCh38.p7 | 7:95494632 | CTTCTTGCCCTCAGT[A/T]TTTTTTCTTTCTGTA | 51666 |
rs183080424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536297 | TCAAGCAATCCTCCT[A/G]CCTCAGTCTCCCAAG | 51666 |
rs183080612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521779 | ACGTAGTTTTTTAAA[A/G]CACAAAATAATAGTA | 51666 |
rs183087954 | snp | C/G | 0.00874735 | 0.0655527 | | | GRCh38.p7 | 7:95477100 | TTTTATCCGCATTGG[C/G]TTGGATTTTTTTTTT | 51666 |
rs183088202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490508 | AATACATGGACACAG[C/G]CAGAGCAAATGTCTG | 51666 |
rs183213941 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540160 | ATTTTTTTATTGGTG[A/G]AATTAAAGTAATTTT | 51666 |
rs183358829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495228 | CAAATAAAATCTTGG[A/G]GTGATAATTTTTTTA | 51666 |
rs183399529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524601 | CACACACAAAGATAC[A/G]TTCAAGTTCCAACCT | 51666 |
rs183533381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521148 | TTGCCTTCAATAAAA[A/T]TTTTATCATTTCCTT | 51666 |
rs183554893 | snp | C/T | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95481578 | CAAATTTCTTCCCTA[C/T]GGTTGCATTTGATAA | 51666 |
rs183608239 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95515604 | TGTTTTTCATAGAGA[C/T]GGGGTTTCCCCATGT | 51666 |
rs183619224 | snp | C/T | | | | | GRCh38.p7 | 7:95477880 | TCTCCACTCCTCTTT[C/T]CCATTCCTAACTGCA | 51666 |
rs183642626 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95507279 | CTGGCTTTTTTTCTA[A/G]AGAGTCAAGACCTAA | 51666 |
rs183656892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95529478 | TAGAAGAAAAGTTCT[A/G]CTAGAGAATTTAAGG | 51666 |