SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1557498 | snp | A/C | 0.029993 | 0.118731 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887493 | aagtagctcactgtc[A/C]ccttgagcCATGATC | 105369632 |
rs1974437 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887038 | aattagccaggcatg[C/G]cggcgtgtgcctgta | 105369632 |
rs1974438 | snp | C/G | 0.117188 | 0.211804 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887153 | aactccagcctgggc[C/G]acagagcaagactct | 105369632 |
rs2269357 | snp | A/C | 0.4884 | 0.0752703 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883871 | TCTTGCCAGACCAGG[A/C]TCTGTGGGCGCGGCC | 105369632 |
rs2269358 | snp | G/T | 0.46281 | 0.131194 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883987 | CTACCCCCTGGGCTG[G/T]AGGGAGGCAGGGCAC | 105369632 |
rs2269359 | snp | A/G | 0.497041 | 0.0383476 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884489 | AAAGCCAGAGTCATC[A/G]CTGACTAGGAGGAAA | 105369632 |
rs2269360 | snp | A/G | 0.345679 | 0.230967 | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884712 | ACTACCCGCCCTCTC[A/G]GTCCCGCAGCCACGA | 105369632 |
rs2365570 | snp | A/G | 0 | 0 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884248 | GGCTGGCATTTACAA[A/G]AAGGTGGCCCAGACC | 105369632 |
rs6489740 | snp | C/T | 0.487568 | 0.077855 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878817 | AGGTGAGCATATATT[C/T]GTTTGTGTAAAAATC | 105369632 |
rs6489741 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890350 | CAGGATGGTCTCGAA[C/T]TCCTGACCTCAGGTG | 105369632 |
rs7132019 | snp | C/T | 0.498676 | 0.0256975 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882958 | ggaataaagtctctt[C/T]cctctgaattccttt | 105369632 |
rs7134129 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888994 | TCACTGTGTTGGCCA[C/G]GCTGTCTTGAACTCC | 105369632 |
rs7138526 | snp | A/G | 0.48446 | 0.0867661 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890100 | TGGTTTTTGTCTTTC[A/G]GTAATGTTTAGTGGC | 105369632 |
rs7294770 | snp | A/G | 0.46875 | 0.121031 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877932 | acatggtgaaatccc[A/G]tctctactaaatata | 105369632 |
rs7295049 | snp | C/G | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878171 | actttgggaggccga[C/G]gcaggtggatcactt | 105369632 |
rs7311510 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878068 | ccactgcactccaac[A/C]tgggcgacagagtga | 105369632 |
rs7314788 | snp | C/T | 0.485561 | 0.0837315 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878008 | ccctcagcaggagaa[C/T]tgtttgaacccagga | 105369632 |
rs7316447 | snp | A/G | 0.459184 | 0.136902 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883038 | gaggccaggagttgg[A/G]gactagcctaggtag | 105369632 |
rs7955412 | snp | C/G | 0.483657 | 0.0889059 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889207 | GGGGAATAGCATTCA[C/G]AAGATCATGAGTTGC | 105369632 |
rs7960576 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877895 | atcacctgaggtcag[C/G]agttcaagaccagcc | 105369632 |
rs7965106 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878745 | aacaagagcgaaact[A/C]catctcaaaaaaaaa | 105369632 |
rs7979695 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878707 | ggtgagctgagattg[A/C]gccattgcactccag | 105369632 |
rs9737885 | snp | A/G | 0.48 | 0.0979796 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881157 | tttttgtatgctttt[A/G]taaagacagggtttc | 105369632 |
rs9737890 | snp | A/T | 0.487369 | 0.07846 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881289 | tcCTTTTAAAAAAAA[A/T]GTCCCCTCCCACCAC | 105369632 |
rs9739707 | snp | C/T | 0.46875 | 0.121031 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881152 | taatttttttgtatg[C/T]ttttataaagacagg | 105369632 |
rs10599968 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877961 | TACAAAAAAAAAAAA[-/A]TTAGCCAGGCGTGGT | 105369632 |
rs10849530 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878899 | ATATATATATATATA[A/T]AAAATGATGTACAAA | 105369632 |
rs10849531 | snp | A/G | 0.494699 | 0.051208 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881384 | TGAACTTTTACATAC[A/G]TATACACTTGGGTGA | 105369632 |
rs11064440 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876385 | CGCGATGGCTCACAC[C/T]TGTAATCCCAGCACT | 105369632 |
rs11064441 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876386 | GCGATGGCTCACACC[G/T]GTAATCCCAGCACTT | 105369632 |
rs11064442 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878901 | ATATATATATATATA[A/T]AATGATGTACAAAAT | 105369632 |
rs11064443 | snp | A/C | 0.160459 | 0.233415 | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882089 | TGATGATACATTCCC[A/C]AGGGTAGCTCCTATT | 105369632 |
rs11064444 | snp | C/T | 0.46875 | 0.121031 | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884725 | TCAGTCCCGCAGCCA[C/T]GAGGAGGACGCTGCC | 105369632 |
rs11064445 | snp | A/G | 0.0883596 | 0.190715 | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885179 | AAACAAAAGAATCCA[A/G]AAGAATTGATGTTTT | 105369632 |
rs11064446 | snp | C/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885770 | AAGCAAATATATTTA[C/G]GCCAGGGTCTCACTG | 105369632 |
rs11064453 | snp | G/T | 0.206111 | 0.246117 | | | GRCh38.p7 | 12:6891487 | AGGGCGGAAACTAGG[G/T]CCCGAGGCTGAAAGT | 105369632 |
rs11287596 | in-del | -/A | 0 | 0 | upstream-variant-2KB, downstream-variant-500B | SPSB2, LOC105369632 | GRCh38.p7 | 12:6875356 | TTTGAGACGGAGTCT[-/A]AGCTCTGATGCCTAG | 105369632 |
rs11377126 | in-del | -/G | 0 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887699 | TGGCCAGGCGCGGTG[-/G]CTCACGCCTGTAATC | 105369632 |
rs11394173 | in-del | -/G | 0 | 0 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889479 | TAGCCGGGATTATAG[-/G]TGCCCATCACCATGC | 105369632 |
rs11402311 | in-del | -/G | 0 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886902 | ATAGCCAGGCGCGGT[-/G]GCTCACGCCTGTAGT | 105369632 |
rs11831556 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883489 | TGCCACTGCACTACA[A/G]ACTGGGCAACAGAGT | 105369632 |
rs11833856 | snp | A/G | 0.46875 | 0.121031 | | | GRCh38.p7 | 12:6891856 | GCTACTCAGGAGGCT[A/G]GGGCAGGAGGATTGC | 105369632 |
rs11836014 | snp | G/T | 0.375 | 0.216506 | | | GRCh38.p7 | 12:6892075 | TAGTTTTCCTTTTTT[G/T]TTTTTTGAGACAGTC | 105369632 |
rs12300574 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880671 | gagactacaggcatg[C/T]gccacaatgcctttt | 105369632 |
rs12304851 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883808 | CACCAACGGAGCCAT[A/G]GAGGGACCTCGGCCC | 105369632 |
rs12310313 | snp | A/G | 0 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888599 | AAACCTTCATTCAGC[A/G]CCTTTATGAGCACAT | 105369632 |
rs12311741 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877087 | agagcaagactccat[C/T]tcaaaaaaaaaaaaa | 105369632 |
rs12814489 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883800 | AGCATTGTCACCAAC[G/T]GAGCCATAGAGGGAC | 105369632 |
rs12814722 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883909 | AGGACTAGGGCGGTG[G/T]CAGTGGCCAGGTGAG | 105369632 |
rs12817264 | snp | C/G | 0.46875 | 0.121031 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884494 | CAGAGTCATCGCTGA[C/G]TAGGAGGAAAACTTC | 105369632 |
rs12822589 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876442 | ctgaggtttggagtt[A/C]gagaccagcctggcc | 105369632 |
rs12831467 | snp | A/C | 0.375 | 0.216506 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886522 | cagaggtccctgcgg[A/C]cttccgcagtgtttg | 105369632 |
rs16932987 | snp | C/G/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885261 | CTCCAAGGATGCAAT[C/G/T]AAAAAGAAATTTCAA | 105369632 |
rs17790774 | snp | G/T | 0.0277723 | 0.11452 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889249 | GGCCTTGTGTTTCTA[G/T]TTTGGAAATATTAAA | 105369632 |
rs34043489 | in-del | -/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880730 | GTCTCAGTGTACTCC[-/C]AGGCTGGAGTGCAGT | 105369632 |
rs34086804 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879960 | AAAAATACATAAAAA[-/A]TTAGCCAGGCCTACT | 105369632 |
rs34759893 | in-del | -/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886936 | GCACTTTGGGAGGCG[-/G]AAAGTGGGTGGATTG | 105369632 |
rs34853861 | in-del | -/A/ACA/AGAG/GG | 0 | 0 | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884616 | TAAAAAAAAAAAAAA[-/A/ACA/AGAG/GG]CGGGTAGGCTCGAGC | 105369632 |
rs35112820 | in-del | -/T | | | | | GRCh38.p7 | 12:6892082 | CCTTTTTTGTTTTTT[-/T]GAGACAGTCTCATTC | 105369632 |
rs35146755 | in-del | -/AG | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884617 | AAAAAAAAAAAAAAC[-/AG]GGGTAGGCTCGAGCC | 105369632 |
rs35266405 | snp | A/C | 0 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876727 | ACAGCCTGAAATAGG[A/C]CAGTAGAAATAAGGA | 105369632 |
rs35300852 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887260 | AATGCAAAAAAAAAA[-/A]TTATTCAGACATTTT | 105369632 |
rs35308991 | in-del | -/A | 0.375 | 0.216506 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880246 | TTTTACTTAAAAATT[-/A]AAAAAAAAAAAAAAT | 105369632 |
rs35867240 | snp | A/G | 0.04875 | 0.148319 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890509 | CTTCACAAATTTTTT[A/G]AATCTTGATTGAATG | 105369632 |
rs35909908 | snp | A/C | 0 | 0 | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875719 | TGTAGAAGATATTCC[A/C]GACAGAAGAGTCCGC | 105369632 |
rs55833876 | in-del | -/AA | 0 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877111 | AAAAAAAAAAAAAAA[-/AA]GAGAAAGGGAAGTTT | 105369632 |
rs56027063 | in-del | -/T | 0 | 0 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890059 | ATAGGCCTGAGCCAC[-/T]TGCACCTGGCCCAGA | 105369632 |
rs56242562 | snp | A/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878427 | TGGCGACAGAGCAAG[A/T]CTCCGTCTCAAAAAA | 105369632 |
rs56407810 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878466 | ATAAAATAAAAATAA[-/A]TTGAGGACCACAAGA | 105369632 |
rs56673052 | snp | A/G | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881272 | TGAGCCACTGCGATC[A/G]GTCCTTTTAAAAAAA | 105369632 |
rs60073448 | in-del | -/TATATA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878895 | ATATATATATATATA[-/TATATA]AAATGATGTACAAAA | 105369632 |
rs60251849 | in-del | -/TATA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878897 | ATATATATATATATA[-/TATA]AAATGATGTACAAAA | 105369632 |
rs61730383 | snp | A/G | 0.101403 | 0.201045 | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885258 | AAGCTCCAAGGATGC[A/G]ATCAAAAAGAAATTT | 105369632 |
rs61750890 | snp | G/T | 0.104938 | 0.20361 | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885141 | AAAAGATTGTTGCTA[G/T]GCTTTGTATGATGCA | 105369632 |
rs66536936 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877949 | CTCTACTAAATATAC[-/A]AAAAAAAAAAAATTA | 105369632 |
rs66933898 | in-del | -/G/TT | 0.5 | 0 | | | GRCh38.p7 | 12:6892075 | TAGTTTTCCTTTTTT[-/G/TT]TTTTTTGAGACAGTC | 105369632 |
rs68038064 | snp | C/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880543 | GGTGACAGAGCGACA[C/T]TCCATCTCAAAAAAA | 105369632 |
rs68189435 | snp | A/G | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888102 | TTTGTTTGTTTGTTT[A/G]TTTATTTATTTATTT | 105369632 |
rs71067144 | in-del | -/G | 0 | 0 | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885492 | GTAGCTGGGATTATA[-/G]GCGTGCGCCACCACA | 105369632 |
rs71416247 | snp | C/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886577 | GAGTGGTGATGACTC[C/T]TAAGGAGCATGCTGC | 105369632 |
rs71450171 | in-del | -/AA | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877089 | GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 105369632 |
rs71450172 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882888 | AGCTTTATTTTTTGG[-/A]AAAAAAAAAAAAATT | 105369632 |
rs71574759 | snp | C/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886586 | TGCTTGAAGGCAGCA[C/T]GCTCCTTAAGAGTCA | 105369632 |
rs73042230 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884456 | CCAGAAATGCCCATC[A/G]GCAATGTCTACAAGG | 105369632 |
rs74350835 | snp | C/G | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878182 | CCGAGGCAGGTGGAT[C/G]ACTTGAGGTCAGGAG | 105369632 |
rs74535607 | snp | G/T | 0.299444 | 0.245062 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890757 | AGGGCTCAGAACTGG[G/T]ACCAAGAGAACATAG | 105369632 |
rs74835578 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883365 | CGGCCAATAAAAAAA[A/T]TTTTTAATTAGTTGG | 105369632 |
rs74995846 | snp | A/C | 0.0327778 | 0.123752 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884577 | ATAGGCACAAAGAGC[A/C]AAGGAAGCTGTAGAA | 105369632 |
rs75044169 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888865 | AATCTCTGCTCACTG[A/C]AAACTCTCCCTCCCA | 105369632 |
rs75283847 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890545 | ATTTTTTGAGGCCGT[A/T]TTTTTTTTTTTTCCA | 105369632 |
rs75343557 | snp | A/G | 0.173299 | 0.237943 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889751 | GCTTCTAAAATCATT[A/G]TGCCATCCTTGGCTG | 105369632 |
rs75381716 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887174 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAGAAA | 105369632 |
rs75530845 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890546 | TTTTTTGAGGCCGTA[A/T]TTTTTTTTTTTCCAC | 105369632 |
rs75535814 | snp | C/T | 0.0649672 | 0.168116 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887519 | TGATCAAGGGATCCT[C/T]GGCTTCAGTCCCTCA | 105369632 |
rs75861577 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882566 | GGTTCAAGCAATTCT[C/T]GTGCTTCAACCTCCT | 105369632 |
rs75930696 | snp | A/G | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879114 | AAGACTATAAATAGC[A/G]TTCAGTGTATACTGC | 105369632 |
rs76205610 | snp | C/T | 0.243194 | 0.249907 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876229 | AACTCCTGAGTCAAG[C/T]GATCCTCCTGCCTCA | 105369632 |
rs76891340 | in-del | -/AT | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880986 | TTTTTATATATATAT[-/AT]TTTGAGACAAGGTCT | 105369632 |
rs77378695 | snp | C/T | 0.299444 | 0.245062 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891145 | CGCCCAGCGCCAATG[C/T]CCCGCCCCGCGCAGC | 105369632 |
rs77599845 | snp | C/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878168 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 105369632 |
rs77900602 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882888 | AGCTTTATTTTTTGG[A/G]AAAAAAAAAAAAATT | 105369632 |
rs78206396 | snp | C/G | 0.206111 | 0.246117 | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884877 | AAAGACTGGAAGCTC[C/G]GCAGAGCAGAACTCT | 105369632 |
rs78279650 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880109 | AGGGAGACTTTGTCT[A/C]AAAAAAAAAAAAAAA | 105369632 |
rs78418597 | snp | C/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886736 | CAGAAGAATTTTTCT[C/T]AGTACATAACAAAAT | 105369632 |
rs78664419 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887579 | ATACCTGGCCAGGCC[A/G]AGAAGTTCTTTACTT | 105369632 |
rs78792797 | snp | G/T | 0.5 | 0 | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885370 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGAT | 105369632 |
rs78793697 | snp | A/C | 0.0811548 | 0.184367 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890979 | AAAATGGCAAAGTCA[A/C]GATCCAACTCCGAAG | 105369632 |
rs78885946 | snp | A/G | 0.0644444 | 0.167538 | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6875911 | GGCCAGTGATGGGGA[A/G]CCACTGTAGGATAGA | 105369632 |
rs79133304 | in-del | -/AA/AAC | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884615 | CTTAAAAAAAAAAAA[-/AA/AAC]CGGGTAGGCTCGAGC | 105369632 |
rs79224239 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881720 | TTAAAAAAACAAAAA[A/C]AAGGCCGGGCGCGGT | 105369632 |
rs79519771 | snp | C/T | 0.0495547 | 0.149404 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891104 | CAACGCTCCGTCCCG[C/T]CTCGCATCAACGCCT | 105369632 |
rs80007360 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888829 | TCTCGCTCTGCAGCC[A/G]CGGCTGGAGTAAAGT | 105369632 |
rs80292188 | snp | G/T | 0.0495547 | 0.149404 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882856 | ACCATGAGGCCTGCA[G/T]AAGAAAAACAAAGGA | 105369632 |
rs80300931 | snp | G/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878162 | AATCTCAGCACTTTG[G/T]GAGGCCGAGGCAGGT | 105369632 |
rs111280843 | snp | A/G | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878517 | GAAAAAAGAAAGGCC[A/G]AGGCAGGCAGATCAC | 105369632 |
rs111314892 | in-del | -/T | 0.5 | 0 | | | GRCh38.p7 | 12:6892068 | TAGTTTTCCTTTTTT[-/T]GTTTTTTGAGACAGT | 105369632 |
rs111332582 | snp | C/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876259 | AGCATCCCAAAGTAC[C/T]GGGATTACAGGCGTG | 105369632 |
rs111412630 | in-del | -/A | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878464 | AAATAAAATAAAAAT[-/A]AATTGAGGACCACAA | 105369632 |
rs111806777 | snp | A/C | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888118 | TTTATTTATTTATTT[A/C]TTGAGACAGGGTCTT | 105369632 |
rs111980062 | snp | C/G | 0.5 | 0 | | | GRCh38.p7 | 12:6891662 | GGTTCCATTGCATCA[C/G]CCCTCAAAATGTTTC | 105369632 |
rs112947941 | snp | A/G | 0.18 | 0.24 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888644 | GTACATCAGTGTGGT[A/G]TTGTTGTGTCCTGCA | 105369632 |
rs113157953 | snp | A/G | 0.444444 | 0.157135 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888106 | TTTGTTTGTTTGTTT[A/G]TTTATTTATTTATTG | 105369632 |
rs113726583 | snp | A/G | 0 | 0 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884513 | GAGGAAAACTTCCAG[A/G]CCTTGTTAGTCTCTG | 105369632 |
rs113974345 | snp | G/T | 0.5 | 0 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888117 | GTTTATTTATTTATT[G/T]ATTGAGACAGGGTCT | 105369632 |
rs114187272 | snp | C/T | 0.096524 | 0.197345 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879619 | GTGACAGAGCGAGAC[C/T]CCGTCTCAAAAAATA | 105369632 |
rs114377948 | snp | A/G | 0.0333238 | 0.124705 | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884480 | TACAAGGAGAAAGCC[A/G]GAGTCATCGCTGACT | 105369632 |
rs114843497 | snp | A/C | 0.234415 | 0.249514 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879780 | ACGCCTGTGCTGCTG[A/C]TGCTGCTGCTGCTGC | 105369632 |
rs115112306 | snp | C/T | 0.182706 | 0.240773 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883904 | GCTGGAGGACTAGGG[C/T]GGTGGCAGTGGCCAG | 105369632 |
rs115364412 | snp | A/G | 0.1264 | 0.217309 | | | GRCh38.p7 | 12:6891407 | CTTCCGTCCCCGCCA[A/G]TCTCTTCTCCGGCCC | 105369632 |
rs115368767 | snp | A/G | 0.0495547 | 0.149404 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879112 | AAAAGACTATAAATA[A/G]CGTTCAGTGTATACT | 105369632 |
rs115805303 | snp | A/G | 0.0168055 | 0.0901129 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883819 | CCATAGAGGGACCTC[A/G]GCCCAAGCTGGGGCC | 105369632 |
rs116219163 | snp | A/C | 0.0811548 | 0.184367 | | | GRCh38.p7 | 12:6891583 | AAGAGAGTGGAATGG[A/C]CTGAGTGCTTGTGAG | 105369632 |
rs116412573 | snp | C/T | 0.0654984 | 0.168698 | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889991 | CTGCAGCCTACAACT[C/T]CTGGCCTCAAGAGGA | 105369632 |
rs116934211 | snp | A/T | 0.0165278 | 0.0893908 | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875740 | AAGAGTCCGCATGAA[A/T]AAAAGCAAGAAGCAG | 105369632 |
rs116963532 | snp | A/T | 0.04875 | 0.148319 | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883079 | CCTCCTTAGCCAATA[A/T]TTTTTTTTTTCTGTT | 105369632 |
rs117172541 | snp | A/G | 0.124444 | 0.216185 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888007 | ACAAAAAACAAAAAA[A/G]AAAAAGAGAAAGAAA | 105369632 |
rs118094308 | snp | A/G | 0.124444 | 0.216185 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881533 | ATGAGCCTGGGCAAC[A/G]TAGGGAGACCTCGTC | 105369632 |
rs138208445 | snp | A/C/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884437 | GGATACTCAGCTGAC[A/C/G]GGACCAGAAATGCCC | 105369632 |
rs138267296 | snp | A/G | | | | | GRCh38.p7 | 12:6891767 | TCCCCGAGGAGGGAG[A/G]TCAGAAGTGGGAGAC | 105369632 |
rs138832667 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890932 | CTGAGGCTTAGAGAA[A/G]TTAAACGTATTGTCC | 105369632 |
rs139181486 | in-del | -/TTTG | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888091 | TCCATTACCTGTTTG[-/TTTG]TTTGTTTGTTTATTT | 105369632 |
rs139524780 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880115 | ACTTTGTCTCAAAAA[A/G]AAAAAAAAAAGGTTG | 105369632 |
rs140123819 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879567 | TAGAATTGGAGGTTG[C/T]GGTGAGCCAAGATCA | 105369632 |
rs140143300 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877178 | AATCAAGATGGAGAT[G/T]ACAGAAAGAGGAGTA | 105369632 |
rs141167225 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889498 | CCCATCACCATGCCC[A/G]GCTAATTTTTGTATT | 105369632 |
rs141176770 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882370 | TTGTATCTGTAAGTC[A/T]TCCATGTTCTTGCAT | 105369632 |
rs141419584 | snp | A/G | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6875870 | CTAGGCTGAGTTAAG[A/G]AATGCAAATGTTTTC | 105369632 |
rs141424051 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877873 | TTTGGGAGGCCGAGG[C/T]GTGTGGATCACCTGA | 105369632 |
rs142082594 | in-del | -/TT | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886842 | TAAAGTCTAAAGTTG[-/TT]TTTTTTTAAAAAAAA | 105369632 |
rs142121085 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882613 | AGGCATGTACTACAA[C/T]GCCTGGATAATTTTT | 105369632 |
rs142290463 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888703 | GTCCTGCTTGACTTC[C/T]AGAATGAAGATATTT | 105369632 |
rs143037555 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879185 | AAGAACTTACTCATA[C/T]AACCAAACACCACCT | 105369632 |
rs143040363 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877830 | AAAATAGGCCGGACG[C/T]GGTGGCTGACGCCTG | 105369632 |
rs143142654 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883243 | TATTTTTAGTACAGA[C/T]AGGGTTTCTCCATGT | 105369632 |
rs143703503 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889105 | TGTTTGTTTTGTTTT[G/T]TTTTTTAAAGGGCAC | 105369632 |
rs143805170 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879950 | CGTCTCTACTAAAAA[A/G]TACATAAAAATTAGC | 105369632 |
rs143902918 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875388 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACC | 105369632 |
rs144038929 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877684 | CCTTGGAAATCCCTT[A/C]GTAGGCTGGGTGCAG | 105369632 |
rs144364731 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876471 | CCAACATGGAGAAAC[A/C]CTGTCTCTACTAAAA | 105369632 |
rs144779124 | snp | C/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885999 | GCATATGGAGGATCC[C/T]GCCAGCCTCTGAGTT | 105369632 |
rs144967890 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877795 | CTAGTGAGACCCCAT[C/G]TCTACCAAATAATAA | 105369632 |
rs145006230 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889666 | TCTAATAGCTCTGAG[G/T]GGGTTGTGCTGTCTG | 105369632 |
rs145031798 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887761 | TCAGTTGAGGTCAGG[A/T]GTTCAAGACCAGCCA | 105369632 |
rs145274394 | in-del | -/CGCTCCTCCC | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891119 | CTCGCATCAACGCCT[-/CGCTCCTCCC]CGCTCCTCCCCGCCC | 105369632 |
rs145292672 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882515 | AGACAGGAGTGCAGT[C/T]GTGCGATCTCGACTC | 105369632 |
rs145390007 | in-del | -/TGAG | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888120 | TATTTATTTATTTAT[-/TGAG]ACAGGGTCTTGCTGT | 105369632 |
rs146139738 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884821 | TGCATCAGATGCCTT[C/T]GAGACATACAACTGG | 105369632 |
rs146166628 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879276 | TAAAGATATGAACCT[A/G]AAACTTGTCATCCAC | 105369632 |
rs146602282 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876799 | GTGACTGATTAGATA[C/T]GGAGTTGAGGCTGGG | 105369632 |
rs147366272 | snp | C/G | | | | | GRCh38.p7 | 12:6891953 | TGACATAGCAAGACC[C/G]TTTCAAAAAGAGGAG | 105369632 |
rs147633813 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888368 | TGCTGGGATTACAGG[C/T]GTGAGACACCACACC | 105369632 |
rs148315784 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883529 | TCTTTTAAAACAAAC[A/T]AACTAATAAACAAAA | 105369632 |
rs148714917 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875466 | GCTGGGACTACAAGC[A/G]TGCACCACCATGCCT | 105369632 |
rs148888617 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888929 | GCTGGGATTACAGGG[A/G]TGTGCCACCATGCCT | 105369632 |
rs149021492 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877825 | ATAATAAAATAGGCC[A/G]GACGCGGTGGCTGAC | 105369632 |
rs149342932 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878432 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAATAAAG | 105369632 |
rs149395352 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885444 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTT | 105369632 |
rs149617460 | snp | A/G | | | | | GRCh38.p7 | 12:6891927 | GCCTGTGAATACTCT[A/G]GGAGGATGGGTGACA | 105369632 |
rs149702581 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880140 | AGGTTGTTTTAAACA[A/G]TTCATCAGTTGATGC | 105369632 |
rs149754101 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888783 | TTGCTAGAGCACAGG[C/T]AGGTTTTTGTTTGTT | 105369632 |
rs150047958 | snp | A/C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880445 | TAGTCCCAGCTACTC[A/C/G]GGAGGCTGAGGCAAG | 105369632 |
rs150270100 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886902 | AATAGCCAGGCGCGG[G/T]GCTCACGCCTGTAGT | 105369632 |
rs150436229 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884378 | TTCCCCAGGAAGCCC[C/T]TGGCCCCCAAGAAGG | 105369632 |
rs150496092 | snp | C/G | | | | | GRCh38.p7 | 12:6891395 | CCTGAACTGCAGCTT[C/G]CGTCCCCGCCAATCT | 105369632 |
rs150529538 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879989 | CTGGCACGTGCCTGT[A/T]GTCCCAGCTACTCAG | 105369632 |
rs150756251 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887314 | TTTATGAAGCTTTAG[A/T]TTGGTCTTTTCCTTT | 105369632 |
rs150892035 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876267 | AAAGTACTGGGATTA[C/T]AGGCGTGAGCCACTG | 105369632 |
rs151213482 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877871 | ACTTTGGGAGGCCGA[C/G]GCGTGTGGATCACCT | 105369632 |
rs180766246 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886366 | TGCAAGAGGCATTCC[C/T]TCCTCTTTTACTAAT | 105369632 |
rs181049842 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882086 | CCCTGATGATACATT[C/T]CCAAGGGTAGCTCCT | 105369632 |
rs181311227 | snp | A/C | | | | | GRCh38.p7 | 12:6892152 | CTGCAACTTCCACTT[A/C]CCAGGTTCAAGCGAT | 105369632 |
rs181406628 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882580 | TCGTGCTTCAACCTC[C/T]TAAGTAGCTGGGACT | 105369632 |
rs181536065 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881603 | GCACGCCTCTAGTCC[A/C]AGTTACTCTGGTGGG | 105369632 |
rs181673611 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877904 | GGTCAGGAGTTCAAG[A/G]CCAGCCTGGCCAACA | 105369632 |
rs181941586 | snp | A/C/G | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886030 | CCCTTAGTATTTATT[A/C/G]ATCATTTGTGGGTGT | 105369632 |
rs182197601 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878401 | CAAGATCCTGCCACT[A/G]CACTCCAGCCTGGCG | 105369632 |
rs182419475 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878082 | CATGGGCGACAGAGT[A/G]ATACTCCATCTCAGA | 105369632 |
rs182505897 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888902 | AGCAATTCTGTCTCA[A/G]CCTCCCGAGTAGCTG | 105369632 |
rs182717610 | snp | A/C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880976 | TGTTTTTAAATTTTT[A/C/T]TATATATATATTTTG | 105369632 |
rs182724282 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876026 | GGAGTAGCGTGATCA[C/T]GACTCATGGCAGCCA | 105369632 |
rs183069942 | snp | A/C | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883577 | TCAGAGAACTTTTTT[A/C]ACAAGTCTTTGGTGG | 105369632 |
rs183204531 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878997 | CCAAACATCATATGT[A/T]CTCATAAGTGGGAGC | 105369632 |
rs183284588 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888792 | CACAGGCAGGTTTTT[A/G]TTTGTTTGTTTTTTT | 105369632 |
rs183360542 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883388 | TTAGTTGGGTGATGG[G/T]GCACACCTGTAGTCC | 105369632 |
rs183589724 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880508 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 105369632 |
rs184090096 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877310 | CACACAAGAAAATGG[C/T]AGGTCTGGAGGCAGA | 105369632 |
rs184114564 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880292 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 105369632 |
rs184336069 | snp | A/C | | | | | GRCh38.p7 | 12:6892011 | CCTGTTACAAAGGTA[A/C]ATGCTCTTTTGTCTA | 105369632 |
rs184575540 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881419 | CACCAAAAAGATCAA[A/G]ATAAAGAATCCAGCT | 105369632 |
rs184705589 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889617 | TGGGATTACAGGCGT[A/G]AGCCACCGTGCCTGG | 105369632 |
rs184756572 | snp | C/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886036 | GTATTTATTAATCAT[C/T]TGTGGGTGTTTCTCG | 105369632 |
rs184963885 | snp | C/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885176 | TTGAAACAAAAGAAT[C/G]CAGAAGAATTGATGT | 105369632 |
rs185001382 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891065 | TTTAAAACCAGGATT[C/T]TCGGTCGCCGTCCCG | 105369632 |
rs185138420 | snp | G/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885725 | ATTGAAAGCTTCCAC[G/T]TTTAATGTTATCCTC | 105369632 |
rs185311469 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882280 | GGTTACAGAGGGAAA[C/T]CTTGTCTCTAAAAAA | 105369632 |
rs185378930 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876605 | GCCGAGATCACGCCA[C/T]TGCACTCCAGCCTGG | 105369632 |
rs185790560 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881726 | AAACAAAAACAAGGC[C/T]GGGCGCGGTGGCTCA | 105369632 |
rs185840811 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878524 | GAAAGGCCGAGGCAG[G/T]CAGATCACCTGAGGT | 105369632 |
rs185876762 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888166 | GGAGTGCAGTAGCAT[G/T]AGCATGGCTCACTGC | 105369632 |
rs186220178 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882717 | CTGCCCCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 105369632 |
rs186679598 | snp | A/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884924 | GAGTGCAAGTTGCTG[A/T]TGAAGTGTGTCGCAT | 105369632 |
rs186692777 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886804 | GTAACAATCTGATCT[A/C]TTTTGCTTTTCCCCA | 105369632 |
rs186952806 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878027 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGT | 105369632 |
rs187036919 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878205 | GTCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 105369632 |
rs187056843 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876058 | AACCTCCTGAGCTCC[A/G]CTGATCCTCCTACCT | 105369632 |
rs187551586 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890136 | TATTTTCTTTTTTCT[G/T]TTTTTTTGAGACGGA | 105369632 |
rs187625930 | snp | A/C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888831 | TCGCTCTGCAGCCGC[A/C/G]GCTGGAGTAAAGTGG | 105369632 |
rs187886578 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885390 | GGAGTCTTGATCTGT[C/T]GCCCAGGCTGGAGTG | 105369632 |
rs188349570 | snp | A/C | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886080 | GTCAGGGTCACAAGA[A/C]AATTGTGGGGAGAGG | 105369632 |
rs188433052 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888938 | ACAGGGGTGTGCCAC[A/C]ATGCCTGGCTAATTT | 105369632 |
rs188478038 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877868 | AGCACTTTGGGAGGC[C/T]GAGGCGTGTGGATCA | 105369632 |
rs188668238 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880329 | GCGGGTGGATCACAA[A/G]GTCAAGAGATCGAGA | 105369632 |
rs188674069 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879025 | AGCTAAGCCATGAGA[A/G]TGCAGAGGCATAAGA | 105369632 |
rs188730664 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880692 | AATGCCTTTTTACTT[A/G]TTTTATTATTTTGTT | 105369632 |
rs188948971 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876593 | AGGTTGCGGTGAGCC[A/G]AGATCACGCCATTGC | 105369632 |
rs189214091 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883468 | AGGCTGCAGGGGCTG[C/T]GAATGTGCCACTGCA | 105369632 |
rs189268940 | snp | C/G | | | | | GRCh38.p7 | 12:6892092 | TTTTTGAGACAGTCT[C/G]ATTCGGACGCCCAGG | 105369632 |
rs189386883 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891230 | GACGCTGACTGTCGC[C/T]GGGCGGCGGTCACGT | 105369632 |
rs189414448 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881928 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 105369632 |
rs189499384 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876796 | TTGGTGACTGATTAG[A/G]TATGGAGTTGAGGCT | 105369632 |
rs189649256 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885743 | TAATGTTATCCTCTT[A/G]CTATATAAATAAAGC | 105369632 |
rs189674224 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882495 | ACAGTCTTGCTCTCT[C/T]GCCCAGACAGGAGTG | 105369632 |
rs189794725 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878052 | GTGAGTCAGGATGGC[A/G]CCACTGCACTCCAAC | 105369632 |
rs189925178 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878218 | GACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCGT | 105369632 |
rs190219472 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878739 | CTGGACAACAAGAGC[A/G]AAACTCCATCTCAAA | 105369632 |
rs190290834 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881591 | GGGTGTGGTGGTGCA[C/T]GCCTCTAGTCCCAGT | 105369632 |
rs190338108 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888467 | CCACATTAAGATTAG[C/G]GTCAGCATCCATGGC | 105369632 |
rs190609487 | snp | C/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875565 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 105369632 |
rs190877559 | snp | A/C | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883551 | TAAACAAAACAAAAC[A/C]AAATTCCTTTTCAGA | 105369632 |
rs191132133 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888874 | TCACTGCAAACTCTC[C/T]CTCCCAGGTTCAAGC | 105369632 |
rs191136432 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885060 | AGAAGGCAAAGAGAT[C/T]TTGGTTGGAGATGTT | 105369632 |
rs191138563 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886936 | AGCACTTTGGGAGGC[A/G]AAAGTGGGTGGATTG | 105369632 |
rs191148946 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876990 | AGCTACTTCGGAGGG[G/T]GAAGCAGGAGAATTG | 105369632 |
rs191414656 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880366 | TGGCTTTAGTAGAGA[C/G]AGTGAAACCCCGTCT | 105369632 |
rs191692648 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881352 | TATATAAAGCACACT[A/G]ATCTTAAATTGCCCA | 105369632 |
rs191969721 | snp | C/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883301 | CTCAGGTGATTCACC[C/G]GCCTTGGCCTCCCAA | 105369632 |
rs192019062 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890722 | GTAGAATCGCTGTCA[C/G]CGTCACAAGATACAA | 105369632 |
rs192280268 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876068 | GCTCCGCTGATCCTC[C/G]TACCTCAGCCTCCTG | 105369632 |
rs192703752 | snp | A/G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889557 | GGCCAGGCTGGTCTC[A/G/T]AACTCCTGACCTCAT | 105369632 |
rs192793855 | snp | C/T | | | | | GRCh38.p7 | 12:6891649 | TTACGTTTTAAAGGG[C/T]TCCATTGCATCAGCC | 105369632 |
rs192823111 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879715 | AGGCCTGGGGACAGA[A/G]AACAGTGCCTGCCCC | 105369632 |
rs193190911 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885570 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT | 105369632 |
rs193252899 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876604 | AGCCGAGATCACGCC[A/T]TTGCACTCCAGCCTG | 105369632 |
rs199623425 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878415 | TGCACTCCAGCCTGG[C/T]GACAGAGCAAGACTC | 105369632 |
rs199697466 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879113 | AAAGACTATAAATAG[C/G]GTTCAGTGTATACTG | 105369632 |
rs200101244 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880944 | TGGGATTACAGGCAT[A/G]AGCCACCATGCCTGG | 105369632 |
rs200896100 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884617 | TAAAAAAAAAAAAAA[C/G]GGGTAGGCTCGAGCC | 105369632 |
rs200896177 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879131 | TCAGTGTATACTGCT[C/T]GGGTGATGGGTGCAC | 105369632 |
rs201071453 | in-del | -/A | 0.00636936 | 0.0560724 | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885222 | GAACTAGCACCTTTG[-/A]AAAAGTAAAATGATC | 105369632 |
rs201088944 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880986 | TTTTTATATATATAT[A/T]TTTTGAGACAAGGTC | 105369632 |
rs201166919 | in-del | -/G | | | upstream-variant-2KB, downstream-variant-500B | SPSB2, LOC105369632 | GRCh38.p7 | 12:6875352 | TTTTTTTGAGACGGA[-/G]TCTAAGCTCTGATGC | 105369632 |
rs201511269 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880564 | CTCAAAAAAAAAAAA[A/T]AAATTATAGATGAGG | 105369632 |
rs201701451 | in-del | -/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881289 | CCTTTTAAAAAAAAA[-/T]GTCCCCTCCCACCAC | 105369632 |
rs201834167 | in-del | -/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887250 | ATATCAGGAATAATG[-/C]AAAAAAAAAATTATT | 105369632 |
rs201856296 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879167 | TCTCACAAATCACCA[C/T]GAAAGAACTTACTCA | 105369632 |
rs202029177 | in-del | -/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878463 | AAAATAAAATAAAAA[-/T]TAATTGAGGACCACA | 105369632 |
rs367653660 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883701 | TCTGATTTCTTTCCA[C/T]AGGGACATTTTATTC | 105369632 |
rs367694834 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876107 | GGACTACAGGTGCAT[A/G]CCGCCATGCCGAGCT | 105369632 |
rs367750800 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882456 | AATATATCTATTGTA[C/T]TGTTGATGGATTTTT | 105369632 |
rs367759750 | snp | A/G | | | | | GRCh38.p7 | 12:6892052 | TTTTAAAAATACTCA[A/G]TTTTTCCTAGTTTTC | 105369632 |
rs367863288 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888804 | TTTGTTTGTTTGTTT[G/T]TTTTGACAGTCTCGC | 105369632 |
rs367877186 | in-del | -/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888323 | TGGTCTTGAACTCTT[-/T]GGACTCAAGAGATCT | 105369632 |
rs367901437 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877360 | GACAGGGATTTGGGA[C/G]GTGTGTCAGTCTTTA | 105369632 |
rs369196689 | in-del | -/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885517 | ACCACACCTGGCTAA[-/T]TTTTGTATTCTTAGT | 105369632 |
rs369203955 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889488 | GATTATAGTGCCCAT[C/T]ACCATGCCCGGCTAA | 105369632 |
rs369254452 | in-del | -/A | | | upstream-variant-2KB, downstream-variant-500B | SPSB2, LOC105369632 | GRCh38.p7 | 12:6875357 | TTGAGACGGAGTCTA[-/A]GCTCTGATGCCTAGG | 105369632 |
rs369313292 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877435 | TGGGGACAAAGAGAG[C/T]GTGGAGCAACAGAAG | 105369632 |
rs369889936 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889689 | GCTGTCTGTTCCTCT[A/G]CAGACACATCTCACC | 105369632 |
rs370312188 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877038 | GAGGCTGCAGTGAGC[C/T]GAGATGGCGCTACCG | 105369632 |
rs370391264 | snp | G/T | | | | | GRCh38.p7 | 12:6892174 | TCAAGCGATTCTGTT[G/T]CCTCAGCCTCCCGAG | 105369632 |
rs370472703 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888000 | TCAAAACACAAAAAA[A/C]AAAAAAAAAAAAGAG | 105369632 |
rs370723799 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891119 | CCTCGCATCAACGCC[C/T]CGCTCCTCCCCGCCC | 105369632 |
rs371097973 | snp | C/T | | | splice-acceptor-variant | LOC105369632 | GRCh38.p7 | 12:6875916 | GTGATGGGGAGCCAC[C/T]GTAGGATAGAAGAAG | 105369632 |
rs371241555 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887699 | CTTGGCCAGGCGCGG[G/T]GCTCACGCCTGTAAT | 105369632 |
rs371323309 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886468 | TATTTCAGACTATCA[C/T]ATGGGGAGAAACCTT | 105369632 |
rs372035839 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880151 | AACAATTCATCAGTT[A/G]ATGCCACTGAATCTG | 105369632 |
rs372302299 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883240 | TTGTATTTTTAGTAC[A/G]GACAGGGTTTCTCCA | 105369632 |
rs372313142 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883973 | CCTCCTCTCTTTCGC[C/T]ACCCCCTGGGCTGGA | 105369632 |
rs372576255 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887659 | GACTTGCACAATGAG[C/T]TTCACTTCTTTGTCA | 105369632 |
rs373226443 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878752 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 105369632 |
rs373737789 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877053 | CGAGATGGCGCTACC[A/G]CACTCCAGCCTGGGC | 105369632 |
rs373875133 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876212 | TGCCCAGGCTGGTCT[C/G]GAACTCCTGAGTCAA | 105369632 |
rs373876893 | in-del | -/TCCTCCCCGC | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891132 | CTCGCTCCTCCCCGC[-/TCCTCCCCGC]CCAGCGCCAATGCCC | 105369632 |
rs373963325 | snp | A/C | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882541 | GACTCACTGCAACCT[A/C]CACCTCCCAGGTTCA | 105369632 |
rs374028121 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883937 | GAGTGCACATGGCTG[G/T]GGGTGGTCCCTCAAT | 105369632 |
rs374914525 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876331 | CCTGGCAGCAACATA[C/G]AGGAGCTTCAAGGGA | 105369632 |
rs375135761 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890058 | TATAGGCCTGAGCCA[A/C]TTGCACCTGGCCCAG | 105369632 |
rs375336571 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889547 | TCACCATGTTGGCCA[C/G]GCTGGTCTCGAACTC | 105369632 |
rs375459833 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885747 | GTTATCCTCTTGCTA[C/T]ATAAATAAAGCAAAT | 105369632 |
rs375868504 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884893 | GCAGAGCAGAACTCT[A/G]AACAACGTGCCTCAG | 105369632 |
rs376232468 | in-del | -/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885355 | AAGTTAGGTGGATCC[-/T]TTTTTTTTTTTTTTG | 105369632 |
rs376270695 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888990 | GGTTTCACTGTGTTG[G/T]CCAGGCTGTCTTGAA | 105369632 |
rs376523554 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891218 | GGGGGCGGGGCAGAC[A/G]CTGACTGTCGCCGGG | 105369632 |
rs376680003 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883485 | AATGTGCCACTGCAC[C/T]ACAAACTGGGCAACA | 105369632 |
rs376731599 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886324 | CCAGGGACAGGCAGG[A/T]GACAGATGCCTTCCT | 105369632 |
rs376932197 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880509 | GTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 105369632 |
rs377372804 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884121 | TGGCCAGCAAAAGCA[A/G]GCTGCATGGCCCACT | 105369632 |
rs377603888 | in-del | -/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890060 | TAGGCCTGAGCCACT[-/T]GCACCTGGCCCAGAC | 105369632 |
rs377647733 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875733 | CAGACAGAAGAGTCC[A/G]CATGAAAAAAAGCAA | 105369632 |
rs377696503 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891181 | AGGTGCCAGTTGCGT[A/G]ACCACGGCAAAGCTC | 105369632 |
rs386375506 | in-del | -/AA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877090 | CAAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 105369632 |
rs386375507 | in-del | -/AA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877110 | AAAAAAAAAAAAAAA[-/AA]AGAGAAAGGGAAGTT | 105369632 |
rs386759955 | multinucleotide-polymorphism | CGT/GGC | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877871 | ACTTTGGGAGGCCGA[CGT/GGC]GTGTGGATCACCTGA | 105369632 |
rs527967537 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883681 | GATTTAACCACATGC[A/T]ATTTTCTGATTTCTT | 105369632 |
rs528343769 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887206 | GAAAAGAAAAGAAAA[A/G]AAATAAAGCCCTGTT | 105369632 |
rs528770243 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881465 | CTCACACCTATAATC[A/C]CAGTACTTTGGGAGG | 105369632 |
rs529573555 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6875923 | GGAGCCACTGTAGGA[C/T]AGAAGAAGAGAGGAA | 105369632 |
rs530118459 | in-del | -/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878751 | AGCGAAACTCCATCT[-/C]AAAAAAAAAAAAAAA | 105369632 |
rs530327569 | snp | C/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875711 | TTGCTGCATGTAGAA[C/G]ATATTCCAGACAGAA | 105369632 |
rs530379690 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889391 | TTGTCCAGGCTGCAG[C/T]GCAGTGGCACGATCT | 105369632 |
rs531568172 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887228 | AGCCCTGTTGAGGAC[G/T]TGTAATATATCAGGA | 105369632 |
rs532094640 | in-del | -/TT | | | upstream-variant-2KB, downstream-variant-500B | SPSB2, LOC105369632 | GRCh38.p7 | 12:6875342 | TTTCTCTTTTTTTTT[-/TT]GAGACGGAGTCTAAG | 105369632 |
rs532489811 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890200 | GGTGCAATCTCGGCT[C/G]ACTGCAACCTCCGCC | 105369632 |
rs532772997 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880315 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACAAGG | 105369632 |
rs532810583 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884349 | TGAAGGAGGACCGCT[C/T]CTCACTCATCCTCTT | 105369632 |
rs533532859 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876505 | CAAAATTAGCCGGGC[A/G]TGGTGGAGCATGCCT | 105369632 |
rs534455981 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890793 | CCATCTTACACTCGC[G/T]CGGAATGGGGGCTGG | 105369632 |
rs535411764 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877972 | AAAAATTAGCCAGGC[A/G]TGGTGGTGTGCACCT | 105369632 |
rs535628620 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880311 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 105369632 |
rs536241642 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888196 | CAGCCTCAACTTTCC[C/T]AGGCACAGGTGATCC | 105369632 |
rs536720692 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886851 | AAAGTTGTTTTTTTA[A/T]AAAAAAAAAAGAAAA | 105369632 |
rs536774909 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885131 | TGCTTCCTGAAAAAG[A/G]TTGTTGCTATGCTTT | 105369632 |
rs538044576 | snp | A/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890636 | AAGTGCTTGATGGCC[A/T]TTCAGATGGATCATG | 105369632 |
rs539099057 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877730 | ATCCCACCACTTTGA[C/G]AGGCTGAAGCAGGAG | 105369632 |
rs541571448 | snp | C/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875732 | CCAGACAGAAGAGTC[C/T]GCATGAAAAAAAGCA | 105369632 |
rs542433920 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877980 | GCCAGGCGTGGTGGT[A/G]TGCACCTGTAATCCC | 105369632 |
rs542643333 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889247 | AGGGCCTTGTGTTTC[C/T]AGTTTGGAAATATTA | 105369632 |
rs543899851 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878325 | GGAGAATCGTGCCTG[G/T]AATCCCAGCTACTCA | 105369632 |
rs544529958 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890012 | CTCAAGAGGATTAGC[C/T]TCTGGTCTTGCCCTC | 105369632 |
rs545263146 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881832 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 105369632 |
rs547061180 | in-del | -/T/TT | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890545 | TTTTTTGAGGCCGTA[-/T/TT]TTTTTTTTTTTTCCA | 105369632 |
rs548307401 | in-del | -/C | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882497 | AGTCTTGCTCTCTCG[-/C]CCAGACAGGAGTGCA | 105369632 |
rs548616878 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887173 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAGAA | 105369632 |
rs548773668 | snp | C/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884524 | CCAGGCCTTGTTAGT[C/G]TCTGTATGGCCCATG | 105369632 |
rs549649483 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882151 | TGTTCTTCAATTTCA[C/T]ATAAATGGAATCATA | 105369632 |
rs549864074 | snp | G/T | | | | | GRCh38.p7 | 12:6891361 | GCTACAGAAACTGGA[G/T]CCCGCCATCGGGCTT | 105369632 |
rs550089333 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878362 | TGAGGCAGAAGAACC[C/G]GCAAGGCAGAGGTTG | 105369632 |
rs550330008 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887216 | GAAAAAAAATAAAGC[A/C]CTGTTGAGGACTTGT | 105369632 |
rs550962728 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884791 | CCTGTGGTGGTGGGC[A/G]AAGATGACCTGTTGT | 105369632 |
rs551742826 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884598 | AGCTGTAGAAGAGGA[C/T]GCTTAAAAAAAAAAA | 105369632 |
rs552324713 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883948 | GCTGTGGGTGGTCCC[A/T]CAATTGCTCCCTCCT | 105369632 |
rs552789456 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887012 | CCCATCTCTACTTTA[A/G]ATATACAAAAAATTA | 105369632 |
rs553406328 | snp | C/T | | | | | GRCh38.p7 | 12:6891825 | GCTGGGGCGATGGCT[C/T]ATGCCTGTGGTCCCA | 105369632 |
rs554523087 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876790 | CAAGATTTGGTGACT[A/G]ATTAGATATGGAGTT | 105369632 |
rs554947264 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889201 | GGTGGAGGGGAATAG[A/C]ATTCAGAAGATCATG | 105369632 |
rs555004757 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890469 | GTTGTCACTTTAGCA[A/G]TTGTAGGAGAATCTG | 105369632 |
rs555291557 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890720 | CAGTAGAATCGCTGT[C/T]AGCGTCACAAGATAC | 105369632 |
rs556031052 | in-del | -/TATATATATATATATAAA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878885 | ATATATATATATATA[-/TATATATATATATATAAA]ATGATGTACAAAATA | 105369632 |
rs556176006 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889104 | TGTTTGTTTTGTTTT[-/G]TTTTTTTAAAGGGCA | 105369632 |
rs556389297 | snp | G/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875737 | CAGAAGAGTCCGCAT[G/T]AAAAAAAGCAAGAAG | 105369632 |
rs556772476 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877867 | CAGCACTTTGGGAGG[C/T]CGAGGCGTGTGGATC | 105369632 |
rs556860279 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882307 | AAAAAAGAAAAAAGA[A/G]AGAAAGAAAAAGAAA | 105369632 |
rs557185396 | in-del | -/AA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877960 | ATACAAAAAAAAAAA[-/AA]TTAGCCAGGCGTGGT | 105369632 |
rs557413555 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881195 | TGCCCAGGTTGGTCT[C/T]GAACTCCTGGGCTCA | 105369632 |
rs558197085 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881028 | CCCAGGCTGGAGTGC[A/G]GTGCACGATCTCGGC | 105369632 |
rs558578898 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883404 | GCACACCTGTAGTCC[A/T]AGTACTCAGGATGCC | 105369632 |
rs559346930 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889410 | GTGGCACGATCTTGA[A/C]TCACTGCAACCTTTG | 105369632 |
rs559613738 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884550 | CCATGCAAATGCCCA[A/G]CTCTTCGGCATATAG | 105369632 |
rs559926821 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888830 | CTCGCTCTGCAGCCG[C/T]GGCTGGAGTAAAGTG | 105369632 |
rs560611720 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879767 | TGAGAATTTAATCAC[A/G]CCTGTGCTGCTGATG | 105369632 |
rs560670865 | snp | A/G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882382 | GTCATCCATGTTCTT[A/G/T]CATGAAATAGCTCAT | 105369632 |
rs561959601 | snp | C/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875554 | TCGAACTCCTGACCT[C/T]GTGATCTGCCCGCCT | 105369632 |
rs562570537 | in-del | -/AAAAG | 0.002414 | 0.0346579 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886862 | TTAAAAAAAAAAAAG[-/AAAAG]AAAAGAAAAGAAAAG | 105369632 |
rs563314647 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886369 | AAGAGGCATTCCTTC[C/T]TCTTTTACTAATCCT | 105369632 |
rs563749516 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878363 | GAGGCAGAAGAACCC[A/G]CAAGGCAGAGGTTGC | 105369632 |
rs564245480 | in-del | -/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878976 | AAGTAACTCAGGAAT[-/G]GAAAACCAAACATCA | 105369632 |
rs564412450 | in-del | -/AAAC | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882006 | AGACTCCATCTCAAA[-/AAAC]AAACAAACAAACAAA | 105369632 |
rs564423839 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878101 | CTCCATCTCAGAAAA[C/G]AAAACAAAAAAATAA | 105369632 |
rs565227719 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884346 | GGCTGAAGGAGGACC[A/G]CTCCTCACTCATCCT | 105369632 |
rs565230611 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886850 | TAAAGTTGTTTTTTT[-/A]AAAAAAAAAAAGAAA | 105369632 |
rs565980086 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880546 | GACAGAGCGACATTC[C/T]ATCTCAAAAAAAAAA | 105369632 |
rs566494211 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890148 | TCTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 105369632 |
rs566628160 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890182 | CCCAAGCTGGAGTGC[A/G]ATGGTGCAATCTCGG | 105369632 |
rs566628254 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888742 | ATCAGGGAAAGTACT[A/G]CAGTCACCCAGGACT | 105369632 |
rs567517826 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884959 | TATGACATGAGAGTT[C/T]GTAAATGCTCCACAC | 105369632 |
rs567680193 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888131 | TTATTGAGACAGGGT[C/T]TTGCTGTATCACCCA | 105369632 |
rs567708186 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886850 | TAAAGTTGTTTTTTT[A/T]AAAAAAAAAAAGAAA | 105369632 |
rs567994531 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876402 | GTAATCCCAGCACTT[C/T]GGAAGGCTGAGATGG | 105369632 |
rs568510054 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890620 | TTCGGTTGAGTGCCT[A/C]AAGTGCTTGATGGCC | 105369632 |
rs568664483 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890727 | ATCGCTGTCAGCGTC[A/C]CAAGATACAAACGAA | 105369632 |
rs569467388 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890428 | CACCGCGCCCGGCCT[G/T]CCATTTTCATTAACC | 105369632 |
rs569728808 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882354 | TTGTGTCTTTCCAGC[A/G]TTGTATCTGTAAGTC | 105369632 |
rs569783054 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880180 | TGGAGCTGGTCAAAC[A/G]TTTGTTGCTAAAAGG | 105369632 |
rs570210444 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876934 | GTCTCTACTAAAAAT[A/G]CAAAAATTAGCTGTG | 105369632 |
rs570287941 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878473 | TAAAAATAATTGAGG[A/G]CCACAAGAACTAGGA | 105369632 |
rs570405060 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889625 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCTATGCC | 105369632 |
rs570842715 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885237 | GAAAAGTAAAATGAT[C/T]TATACAAGCTCCAAG | 105369632 |
rs571705239 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883508 | GGGCAACAGAGTAAG[A/T]CCCTGTCTTTTAAAA | 105369632 |
rs572316383 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889079 | GAGCCACCGTACCGC[C/T]GTTTTTTGTTTGTTT | 105369632 |
rs572388633 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878058 | CAGGATGGCGCCACT[C/G]CACTCCAACATGGGC | 105369632 |
rs572848350 | snp | C/G | | | | | GRCh38.p7 | 12:6891391 | TTCCCCTGAACTGCA[C/G]CTTCCGTCCCCGCCA | 105369632 |
rs572986441 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889463 | TCTGCCTCAGCCTCC[C/G]AGTAGCCGGGATTAT | 105369632 |
rs573074621 | snp | C/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884048 | ACTTCCACAAGGACT[C/G]GCAGTGGTGTGGCCA | 105369632 |
rs573141476 | snp | G/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885202 | GATGTTTTCTTGTGG[G/T]CATCAGAACTAGCAC | 105369632 |
rs573533561 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886373 | GGCATTCCTTCCTCT[G/T]TTACTAATCCTCCTC | 105369632 |
rs574739255 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887842 | TAATACAAAAATTAG[C/T]CAGGCATGGTGGCAC | 105369632 |
rs575008223 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883682 | ATTTAACCACATGCA[A/G]TTTTCTGATTTCTTT | 105369632 |
rs575902297 | snp | A/C | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885562 | ACCATATTGGTCAGG[A/C]TGGTCTCGAACTCCT | 105369632 |
rs576210724 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875738 | AGAAGAGTCCGCATG[A/G]AAAAAAGCAAGAAGC | 105369632 |
rs577382032 | in-del | -/TA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886849 | CTAAAGTTGTTTTTT[-/TA]AAAAAAAAAAAGAAA | 105369632 |
rs745663497 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882505 | TCTCTCGCCCAGACA[A/G]GAGTGCAGTCGTGCG | 105369632 |
rs745668034 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880037 | ACCACTTGAACCCAG[C/G]AGGCGGAGGTTGCAG | 105369632 |
rs746313224 | in-del | -/GTGATGG | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6875901 | CCATAGGACAGGCCA[-/GTGATGG]GGAGCCACTGTAGGA | 105369632 |
rs746488376 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881715 | CTGTCTTAAAAAAAC[A/G]AAAACAAGGCCGGGC | 105369632 |
rs746613044 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879991 | GGCACGTGCCTGTAG[G/T]CCCAGCTACTCAGGA | 105369632 |
rs747121883 | snp | G/T | | | | | GRCh38.p7 | 12:6892031 | TCTTTTGTCTATCCT[G/T]GCTATTTTTAAAAAT | 105369632 |
rs747629103 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879828 | AACATGGTTGTTGGC[C/T]GGGCACAGTGGCTCA | 105369632 |
rs747689350 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876329 | ACCCTGGCAGCAACA[C/T]AGAGGAGCTTCAAGG | 105369632 |
rs749092412 | in-del | -/AA | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884887 | AGCTCGGCAGAGCAG[-/AA]CTCTGAACAACGTGC | 105369632 |
rs749871528 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888530 | TATGTGGCTTTGAAA[C/G]AGCAAATAATGCTTA | 105369632 |
rs750009570 | snp | C/G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891095 | GCCCAGCGCCAACGC[C/G/T]CCGTCCCGCCTCGCA | 105369632 |
rs750811856 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880974 | GCTGTTTTTAAATTT[A/T]TATATATATATATTT | 105369632 |
rs752027166 | snp | C/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875617 | AGCCACCGCGCCCAG[C/G]CTGGGCTGAATCTAA | 105369632 |
rs752407528 | snp | C/G | | | | | GRCh38.p7 | 12:6891698 | CCAGCCCTCTTTCTT[C/G]TATCATGGTGGTTAT | 105369632 |
rs753136211 | in-del | -/TGTT | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888084 | GTTGCTTCCATTACC[-/TGTT]TGTTTGTTTGTTTGT | 105369632 |
rs753504435 | snp | C/T | | | | | GRCh38.p7 | 12:6891513 | AAAGTCCGTTCTTGG[C/T]GGCGAGGGCCGCCGC | 105369632 |
rs753699683 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888875 | CACTGCAAACTCTCC[C/T]TCCCAGGTTCAAGCA | 105369632 |
rs754757585 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888919 | CTCCCGAGTAGCTGG[A/G]ATTACAGGGGTGTGC | 105369632 |
rs754847559 | in-del | -/T | | | | | GRCh38.p7 | 12:6891632 | TACCTACTAAAGTTC[-/T]TTTACGTTTTAAAGG | 105369632 |
rs755882456 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884646 | CCGCTGCATCAGCTT[C/T]GCGCTGGGTCTCTCG | 105369632 |
rs756447053 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881093 | TTTCCCGCCTCAGCC[C/T]CTGGAGTAGCTGGGA | 105369632 |
rs757637544 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875694 | TGGAGGTTGGGTTAC[A/G]GTTGCTGCATGTAGA | 105369632 |
rs757839706 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879845 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCACCA | 105369632 |
rs758425998 | snp | A/G | | | | | GRCh38.p7 | 12:6891826 | CTGGGGCGATGGCTC[A/G]TGCCTGTGGTCCCAG | 105369632 |
rs759438799 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877841 | GACGCGGTGGCTGAC[A/G]CCTGTAATCCCAGCA | 105369632 |
rs759876923 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888040 | CTTAAAATTCTGAAC[-/A]CATTCCACATGCATT | 105369632 |
rs760046146 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891147 | CCCAGCGCCAATGCC[A/C]CGCCCCGCGCAGCCG | 105369632 |
rs760471572 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877030 | GGGAGGTGGAGGCTG[C/T]AGTGAGCCGAGATGG | 105369632 |
rs761009820 | in-del | -/ATTACTGGCATGAGCCACC | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887545 | CCTCAAAGTGCTGGG[-/ATTACTGGCATGAGCCACC]ATACCTGGCCAGGCC | 105369632 |
rs761971658 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883282 | CTGGTCTCGAACTCC[C/T]GATCTCAGGTGATTC | 105369632 |
rs762167962 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880907 | ACTCAAGCAATTCTC[C/T]TGCCTCGTCCTCCCA | 105369632 |
rs764506458 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890688 | TAAAACACTACAATC[C/T]AGTTTAAGACATAAA | 105369632 |
rs765175961 | snp | C/T | | | | | GRCh38.p7 | 12:6891688 | GTTTCCTTCCCCAGC[C/T]CTCTTTCTTCTATCA | 105369632 |
rs767002813 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888161 | AGGCTGGAGTGCAGT[A/G]GCATGAGCATGGCTC | 105369632 |
rs768686452 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883182 | TGCCTCAGCCTCCCG[A/T]GTAGCTGGGATTACA | 105369632 |
rs770545664 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879994 | ACGTGCCTGTAGTCC[C/T]AGCTACTCAGGAAGC | 105369632 |
rs770676244 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877068 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 105369632 |
rs771024508 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887719 | ACGCCTGTAATCCCA[A/G]CACTTTAGGAGGCCG | 105369632 |
rs771237728 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889862 | TCTCTTTTTTTGCCA[C/T]GTCTTGCCATTGTAA | 105369632 |
rs771884918 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889615 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 105369632 |
rs772155247 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885557 | GTTTCACCATATTGG[C/T]CAGGCTGGTCTCGAA | 105369632 |
rs772797258 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876773 | AAACACTGATGAAAC[A/G]GCAAGATTTGGTGAC | 105369632 |
rs773331155 | snp | C/G | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886005 | GGAGGATCCTGCCAG[C/G]CTCTGAGTTCCCTTA | 105369632 |
rs774551105 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880901 | TCCTGTACTCAAGCA[A/G]TTCTCCTGCCTCGTC | 105369632 |
rs775997120 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890444 | CCATTTTCATTAACC[A/G]CATATCTTCGTTGTC | 105369632 |
rs776327545 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879998 | GCCTGTAGTCCCAGC[A/T]ACTCAGGAAGCCGAG | 105369632 |
rs776651323 | in-del | -/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877157 | GATTGGAAGGTGGTG[-/C]CCACCAATCAAGATG | 105369632 |
rs776773016 | in-del | -/TC | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889900 | ATTTCTTTTTGGTTT[-/TC]TTTCTTTTTAATATA | 105369632 |
rs777436124 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879939 | TGGTGAAACCCCGTC[G/T]CTACTAAAAAATACA | 105369632 |
rs777946255 | snp | A/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889708 | ACACATCTCACCAAT[A/T]GTTTGTGTGTTTTTG | 105369632 |
rs778137033 | snp | C/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875540 | TGCCCAGGCTGGCCT[C/T]GAACTCCTGACCTCG | 105369632 |
rs778328042 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876034 | GTGATCACGACTCAT[A/G]GCAGCCACAACCTCC | 105369632 |
rs778936474 | snp | C/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885234 | TTTGAAAAGTAAAAT[C/G]ATCTATACAAGCTCC | 105369632 |
rs780601258 | in-del | -/AA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879235 | AAATAAAATAATAAT[-/AA]AAAGAAGAAGAAAGC | 105369632 |
rs781785652 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889824 | AGGTTTGAACTATGA[C/T]TTGAGATGAAGAGTT | 105369632 |
rs781788265 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885257 | CAAGCTCCAAGGATG[C/T]AATCAAAAAGAAATT | 105369632 |
rs781790726 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887370 | TTCCTCAAGATTTTT[C/T]ATTAGTGTTTCTCTG | 105369632 |
rs781798227 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888541 | GAAACAGCAAATAAT[C/G]CTTAGATCAGCAGAG | 105369632 |
rs781801727 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877214 | GGGCAGGGGCAGGAG[A/G]GTGGGAGAGGGAGAT | 105369632 |
rs781801814 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882934 | CTGCTGGTTTACACA[C/T]TGTTCACTGGAATAA | 105369632 |
rs781804617 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876500 | AAATACAAAATTAGC[C/T]GGGCATGGTGGAGCA | 105369632 |
rs781808046 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880325 | CGAGGCGGGTGGATC[A/T]CAAGGTCAAGAGATC | 105369632 |
rs781809839 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882585 | CTTCAACCTCCTAAG[G/T]AGCTGGGACTTCAGG | 105369632 |
rs781816231 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877073 | CCAGCCTGGGCGACA[A/G]AGCAAGACTCCATCT | 105369632 |
rs781817162 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889151 | GACAGCCCTGTAGAA[C/T]TACACTGCCCCTGCA | 105369632 |
rs781822142 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884854 | ATGTGAGATAGGAAA[C/T]TGAATGTAAAGACTG | 105369632 |
rs781825664 | snp | A/C | | | | | GRCh38.p7 | 12:6892128 | GTGCAGTGGCTTGAA[A/C]TTGGTTCACTGCAAC | 105369632 |
rs781826761 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6875946 | GAGAGGAACATGGTC[A/C]GATAGGCATTTGATT | 105369632 |
rs781830030 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880270 | AAAAAATTGGCCGGG[C/T]ATGGTGGCTCACACC | 105369632 |
rs781831164 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878984 | CAGGAATGGAAAACC[A/T]AACATCATATGTTCT | 105369632 |
rs781837890 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890288 | TCCGTCACCACGCCC[A/G]GCTAATTTTTGCATT | 105369632 |
rs781838035 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881268 | GGGGTGAGCCACTGC[G/T]ATCGGTCCTTTTAAA | 105369632 |
rs781838300 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885628 | GCTGGGATTACAGGC[A/G]TGAGCCAGCATGCCT | 105369632 |
rs781843705 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879904 | CTGAGATAAGGAGTT[C/T]GAGACCAGCCTGGCC | 105369632 |
rs781849509 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881961 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCCAGC | 105369632 |
rs781850182 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886422 | GTGTCGGGATGGGGG[A/G]TGGTCAGGTCTTTCC | 105369632 |
rs781854481 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876600 | GGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 105369632 |
rs781857325 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879768 | GAGAATTTAATCACG[C/T]CTGTGCTGCTGATGC | 105369632 |
rs781861159 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884587 | AGAGCCAAGGAAGCT[A/G]TAGAAGAGGACGCTT | 105369632 |
rs781864527 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887250 | TATCAGGAATAATGC[-/A]AAAAAAAAAATTATT | 105369632 |
rs781865450 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880377 | GAGACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 105369632 |
rs781869153 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884997 | AATCAAGAAAAGAAC[A/G]AAGGCTGTCATTTTT | 105369632 |
rs781869473 | snp | A/G | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886241 | CCCACCTCCAGCCCT[A/G]AGGCGGTTTTTCCCT | 105369632 |
rs781875089 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888260 | AGGTGCACACCACCA[C/T]GTTCAGCTAATTTTC | 105369632 |
rs781876645 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885757 | TGCTATATAAATAAA[A/G]CAAATATATTTAGGC | 105369632 |
rs781883694 | snp | C/T | | | | | GRCh38.p7 | 12:6892025 | AAATGCTCTTTTGTC[C/T]ATCCTTGCTATTTTT | 105369632 |
rs781884241 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888120 | TATTTATTTATTTAT[G/T]GAGACAGGGTCTTGC | 105369632 |
rs781889337 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884168 | CCCATAGTAAGGTGC[C/T]CCATGCTGAGGCATC | 105369632 |
rs781892498 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891329 | GGGCTCTCCTCCCAG[C/T]AGTTCACTCCTTAGT | 105369632 |
rs781895877 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886540 | TCCGCAGTGTTTGTG[C/T]CCCTGGGTACTTGAG | 105369632 |
rs781900562 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882537 | TCTCGACTCACTGCA[A/T]CCTCCACCTCCCAGG | 105369632 |
rs781903160 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883807 | TCACCAACGGAGCCA[C/T]AGAGGGACCTCGGCC | 105369632 |
rs781906537 | snp | G/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875376 | CTGATGCCTAGGCTG[G/T]AGTGCAGTGGCGTGA | 105369632 |
rs781911165 | snp | A/G | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6875897 | TTTCCCATAGGACAG[A/G]CCAGTGATGGGGAGC | 105369632 |
rs781916977 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875566 | CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 105369632 |
rs781918183 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877289 | AGCAAATGGAACCAT[C/T]CAGAACACACAAGAA | 105369632 |
rs781920460 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891114 | TCCCGCCTCGCATCA[A/G]CGCCTCGCTCCTCCC | 105369632 |
rs781923080 | snp | A/G | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885892 | CCTCCACACCTGTGG[A/G]TGTTTCTCGTAAGGT | 105369632 |
rs781924510 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887614 | CCTCAATGATGTATA[A/G]ACAAAGCCATCACGA | 105369632 |
rs781929989 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884418 | CTGCTGAAGAACTCG[A/G]ACTGGATACTCAGCT | 105369632 |
rs781936505 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886808 | CAATCTGATCTCTTT[A/T]GCTTTTCCCCACATA | 105369632 |
rs781938002 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887653 | CTAGGCGACTTGCAC[A/G]ATGAGTTTCACTTCT | 105369632 |
rs781943160 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890188 | CTGGAGTGCAATGGT[G/T]CAATCTCGGCTCACT | 105369632 |
rs781944378 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883788 | CGCCATAGGCCTAGC[A/G]TTGTCACCAACGGAG | 105369632 |
rs781948282 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886710 | GGTTATAGATTAACA[C/G]AATCTCAAGGCAGAA | 105369632 |
rs781948587 | in-del | -/TGTT | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888088 | CTTCCATTACCTGTT[-/TGTT]TGTTTGTTTGTTTGT | 105369632 |
rs781950411 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880110 | GGGAGACTTTGTCTC[A/C]AAAAAAAAAAAAAAA | 105369632 |
rs781955471 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889843 | AGATGAAGAGTTTTT[G/T]TCTTCTCTTTTTTTG | 105369632 |
rs781956591 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887587 | CCAGGCCAAGAAGTT[C/T]TTTACTTTCTTCCTC | 105369632 |
rs781960475 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891096 | CCCAGCGCCAACGCT[C/T]CGTCCCGCCTCGCAT | 105369632 |
rs781961398 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876624 | ACTCCAGCCTGGGCA[A/G]CAAGAGTGAAACTCT | 105369632 |
rs781965196 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877840 | GGACGCGGTGGCTGA[C/T]GCCTGTAATCCCAGC | 105369632 |
rs781966612 | snp | A/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886137 | GTCTTTGCATCATAG[A/T]CAATGTAAAGGATTA | 105369632 |
rs781967330 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887452 | ACTGGGTCTTACTCT[G/T]TCACACAGGCTGGAG | 105369632 |
rs781975704 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889525 | TATTATTAGTAGAGA[C/T]GGCATTTCACCATGT | 105369632 |
rs781975831 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890971 | AGAACTGGAAAATGG[C/G]AAAGTCAAGATCCAA | 105369632 |
rs781978371 | snp | A/G | | | | | GRCh38.p7 | 12:6891615 | AACTTCCTAATTGAG[A/G]CTTACCTACTAAAGT | 105369632 |
rs781986426 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876752 | TAAGGATGAAAATAA[C/T]TCAAGAAACACTGAT | 105369632 |
rs781987000 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886881 | AGAAAAGAAAAGAAA[A/T]AAGAAAATAGCCAGG | 105369632 |
rs781987265 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889431 | GCAACCTTTGCCTCC[C/T]GGGTTCAAGCAATTC | 105369632 |
rs781991631 | snp | C/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875552 | CCTCGAACTCCTGAC[C/G]TCGTGATCTGCCCGC | 105369632 |
rs781992432 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890369 | TGACCTCAGGTGGAC[C/T]ACCCACCTCGGCCTC | 105369632 |
rs781993866 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876118 | GCATACCGCCATGCC[A/G]AGCTAATTTATTTTT | 105369632 |
rs781994429 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885711 | ATTCAGTGCCACAAA[C/T]TGAAAGCTTCCACGT | 105369632 |
rs782005871 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891252 | CGGTCACGTGAGCGG[A/G]AGCGCAGCAGGCCGG | 105369632 |
rs782007948 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879139 | TACTGCTTGGGTGAT[A/G]GGTGCACCAAAATCT | 105369632 |
rs782009180 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881507 | GATCACTTGAGCTCA[A/G]GAGTTCTGAGATGAG | 105369632 |
rs782011353 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884286 | TCTCTGAGGATGCAA[A/G]GAGGAGGAACCAGTC | 105369632 |
rs782016503 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882134 | TATAGATTAGTGTTG[A/T]CTGTTCTTCAATTTC | 105369632 |
rs782016946 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879326 | CAGTATGTGACATCA[A/G]TAATAACATCATGAC | 105369632 |
rs782018797 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876772 | GAAACACTGATGAAA[C/T]GGCAAGATTTGGTGA | 105369632 |
rs782020416 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888610 | CAGCGCCTTTATGAG[C/T]ACATTCATAAAGTGT | 105369632 |
rs782026908 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884661 | CGCGCTGGGTCTCTC[A/G]GTCCCGCAGCCATGA | 105369632 |
rs782030913 | in-del | -/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890546 | TTTTTTGAGGCCGTA[-/T]TTTTTTTTTTTCCAC | 105369632 |
rs782031755 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880591 | GAGGTCTTGCTATTT[C/T]GCCCAGGCTGGACTC | 105369632 |
rs782032536 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887552 | GTGCTGGGATTACTG[C/G]CATGAGCCACCATAC | 105369632 |
rs782033160 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875660 | GAATTGGCCTGAGAC[A/G]AGCCACTTCTCTGCA | 105369632 |
rs782035544 | snp | A/C | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885280 | AAGAAATTTCAAGGC[A/C]TAAAACATGAATGGC | 105369632 |
rs782038237 | snp | A/G | | | | | GRCh38.p7 | 12:6891671 | GCATCAGCCCTCAAA[A/G]TGTTTCCTTCCCCAG | 105369632 |
rs782043828 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883849 | CTCTTCATTGTCGAA[G/T]AAGGCCTCTTGCCAG | 105369632 |
rs782043918 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885681 | GCCTTTGAAGGATGC[C/T]CTGTGTAGATCATCA | 105369632 |
rs782044641 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886449 | TTCCCTTCCCACGAG[A/G]CCATATTTCAGACTA | 105369632 |
rs782050182 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891257 | ACGTGAGCGGGAGCG[A/C]AGCAGGCCGGCGGTC | 105369632 |
rs782051604 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888001 | CAAAACACAAAAAAC[-/A]AAAAAAAAAAAGAGA | 105369632 |
rs782054023 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876982 | GTAATCCCAGCTACT[G/T]CGGAGGGTGAAGCAG | 105369632 |
rs782059658 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883799 | TAGCATTGTCACCAA[C/T]GGAGCCATAGAGGGA | 105369632 |
rs782060071 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888818 | TTTTTTGACAGTCTC[A/G]CTCTGCAGCCGCGGC | 105369632 |
rs782062082 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880157 | TCATCAGTTGATGCC[A/G]CTGAATCTGGAGCTG | 105369632 |
rs782062669 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889995 | AGCCTACAACTCCTG[A/G]CCTCAAGAGGATTAG | 105369632 |
rs782064772 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878644 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 105369632 |
rs782068829 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881131 | CGCCCCGCCAGCATG[C/G]CTGGATAATTTTTTT | 105369632 |
rs782077426 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889722 | TAGTTTGTGTGTTTT[C/T]GAGGTTTAAATGGGC | 105369632 |
rs782086714 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882421 | TTGTCATATAGTATT[C/T]CATCATCTAAATATA | 105369632 |
rs782094102 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877075 | AGCCTGGGCGACAGA[G/T]CAAGACTCCATCTCA | 105369632 |
rs782094667 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887779 | TCAAGACCAGCCAGG[A/C]CAACATGGTGAAATA | 105369632 |
rs782098445 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881793 | GTGGATCACGAGGTC[A/G]GGAGATCGAGACCAT | 105369632 |
rs782101610 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880282 | GGGCATGGTGGCTCA[A/C]ACCTGTAATCCCAGC | 105369632 |
rs782103028 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882577 | TTCTCGTGCTTCAAC[C/T]TCCTAAGTAGCTGGG | 105369632 |
rs782109795 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877052 | CCGAGATGGCGCTAC[C/T]GCACTCCAGCCTGGG | 105369632 |
rs782114968 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884757 | AGACTCACTACCCGC[C/T]GGCTCCCTCCCCCGC | 105369632 |
rs782118221 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880786 | TCACCCCAGCCTCCT[G/T]AGTAGCTAGGACTAC | 105369632 |
rs782122040 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887768 | AGGTCAGGAGTTCAA[A/G]ACCAGCCAGGCCAAC | 105369632 |
rs782130833 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881191 | ATGTTGCCCAGGTTG[G/T]TCTCGAACTCCTGGG | 105369632 |
rs782132998 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884065 | CAGTGGTGTGGCCAT[A/G]TGGCTCAGCCAGCCC | 105369632 |
rs782137270 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881897 | TAGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 105369632 |
rs782138001 | snp | C/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883998 | GCTGGAGGGAGGCAG[C/G]GCACCCAGCCGGAAT | 105369632 |
rs782143061 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882555 | TCCACCTCCCAGGTT[C/T]AAGCAATTCTCGTGC | 105369632 |
rs782144678 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885423 | GTGACAGGATCTCGG[C/T]TCACTGCAACCTCTG | 105369632 |
rs782146097 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884566 | CTCTTCGGCATATAG[A/G]CACAAAGAGCCAAGG | 105369632 |
rs782147461 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886294 | ATCGGGTTTTATACC[A/G]AGACATTCCATTGCC | 105369632 |
rs782147473 | snp | C/T | | | | | GRCh38.p7 | 12:6891820 | TGGTAGCTGGGGCGA[C/T]GGCTCATGCCTGTGG | 105369632 |
rs782153304 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882603 | CTGGGACTTCAGGCA[C/T]GTACTACAACGCCTG | 105369632 |
rs782156670 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890614 | TGTTTCTTCGGTTGA[C/G]TGCCTAAAGTGCTTG | 105369632 |
rs782157724 | snp | C/T | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6877551 | GAGAGACAGCACATG[C/T]GGGGACTGGTAGGTG | 105369632 |
rs782159147 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884945 | TGTGTCGCATTTTTT[A/G]TGACATGAGAGTTCG | 105369632 |
rs782164845 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887675 | TTCACTTCTTTGTCA[A/G]TAGAAACCCTTGGCC | 105369632 |
rs782166843 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876325 | AACCACCCTGGCAGC[A/G]ACATAGAGGAGCTTC | 105369632 |
rs782167083 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880041 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 105369632 |
rs782169493 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890378 | GTGGACCACCCACCT[C/T]GGCCTCCCAAAGTGC | 105369632 |
rs782170156 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884832 | CCTTTGAGACATACA[A/G]CTGGAGATGTGAGAT | 105369632 |
rs782170654 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885303 | TGAATGGCAAACAAA[C/T]GGACCAGAAGATCTC | 105369632 |
rs782171212 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878989 | ATGGAAAACCAAACA[C/T]CATATGTTCTCATAA | 105369632 |
rs782173545 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879184 | AAAGAACTTACTCAT[A/G]TAACCAAACACCACC | 105369632 |
rs782177831 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876645 | GTGAAACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 105369632 |
rs782180629 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886452 | CCTTCCCACGAGGCC[A/G]TATTTCAGACTATCA | 105369632 |
rs782181412 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884141 | CATGGCCCACTGATA[C/T]GGGCCCATCCACCCA | 105369632 |
rs782184184 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879928 | CCTGGCCTACATGGT[A/G]AAACCCCGTCTCTAC | 105369632 |
rs782187370 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883562 | AAACCAAATTCCTTT[C/T]CAGAGAACTTTTTTC | 105369632 |
rs782191765 | in-del | -/C | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882865 | CCTGCAGAAGAAAAA[-/C]AAAGGAGAGCTTTAT | 105369632 |
rs782192132 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889830 | GAACTATGACTTGAG[A/G]TGAAGAGTTTTTTTC | 105369632 |
rs782195501 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884644 | AGCCGCTGCATCAGC[C/T]TCGCGCTGGGTCTCT | 105369632 |
rs782197233 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887477 | CTGGAGTGCAGTGGC[A/G]AAGTAGCTCACTGTC | 105369632 |
rs782197369 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884953 | ATTTTTTATGACATG[A/G]GAGTTCGTAAATGCT | 105369632 |
rs782200346 | snp | A/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875714 | CTGCATGTAGAAGAT[A/T]TTCCAGACAGAAGAG | 105369632 |
rs782201203 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889371 | TGAGATGGAGTCTTG[C/T]GCTGTTGTCCAGGCT | 105369632 |
rs782202993 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890999 | CAACTCCGAAGAGCC[C/T]CCCCCTGCCCACTAG | 105369632 |
rs782205543 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883768 | GGTCATCGGGCTCTG[C/T]CCACCGCCATAGGCC | 105369632 |
rs782206125 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888552 | TAATGCTTAGATCAG[C/G]AGAGTGAAGGATGGA | 105369632 |
rs782207591 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878266 | AAATTAGCTGGGCGT[G/T]GTGGCATGTGCCTAT | 105369632 |
rs782209560 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888321 | GGCTGGTCTTGAACT[C/T]TTGGACTCAAGAGAT | 105369632 |
rs782211573 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891069 | AAACCAGGATTCTCG[A/G]TCGCCGTCCCGCCCA | 105369632 |
rs782216931 | snp | C/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885780 | ATTTAGGCCAGGGTC[C/T]CACTGAGGGGAGCTG | 105369632 |
rs782221274 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884301 | GGAGGAGGAACCAGT[C/T]CACCCAGGCCCTGCA | 105369632 |
rs782226078 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888268 | ACCACCACGTTCAGC[C/T]AATTTTCTGCAGAGA | 105369632 |
rs782226430 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889162 | AGAACTACACTGCCC[C/T]TGCACTTGGGGGCAA | 105369632 |
rs782230284 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | SPSB2, LOC105369632 | GRCh38.p7 | 12:6875317 | TCACACCTTCACACT[A/G]GGCTGAATCTTTCTC | 105369632 |
rs782230878 | snp | C/T | | | | | GRCh38.p7 | 12:6892133 | GTGGCTTGAACTTGG[C/T]TCACTGCAACTTCCA | 105369632 |
rs782231643 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886763 | AAATGGAGTCTCCTA[G/T]GTCTACTTCTTTCTA | 105369632 |
rs782232443 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884677 | GTCCCGCAGCCATGA[C/G]GAGGACGCTGCCCAG | 105369632 |
rs782235941 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890137 | ATTTTCTTTTTTCTT[C/T]TTTTTTGAGACGGAG | 105369632 |
rs782238853 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886551 | TGTGTCCCTGGGTAC[C/T]TGAGATTAGGGAGTG | 105369632 |
rs782240134 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890047 | AGGGCTGGGATTATA[G/T]GCCTGAGCCACTTGC | 105369632 |
rs782248567 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891087 | GCCGTCCCGCCCAGC[G/T]CCAACGCTCCGTCCC | 105369632 |
rs782252343 | in-del | -/ATT | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881246 | TCTCAAAATATTGTG[-/ATT]ATTACAGGGGTGAGC | 105369632 |
rs782258056 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876601 | GTGAGCCGAGATCAC[A/G]CCATTGCACTCCAGC | 105369632 |
rs782259293 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877465 | GGGTCAAGGAGAATA[A/G]AACAAGGTAGAAAAT | 105369632 |
rs782259840 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882003 | AGCAAGACTCCATCT[C/T]AAAAAACAAACAAAC | 105369632 |
rs782261570 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882650 | TTAGTAGAGATGGGG[C/T]TTCACCATGTTGGCC | 105369632 |
rs782261794 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884246 | GTGGCTGGCATTTAC[A/G]AGAAGGTGGCCCAGA | 105369632 |
rs782264158 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879579 | TTGCGGTGAGCCAAG[A/G]TCAGGCCACTGCACT | 105369632 |
rs782264703 | snp | A/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885804 | GGAGCTGTCTTGTCA[A/T]CTTTTAGAGTAAACT | 105369632 |
rs782271800 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876514 | CCGGGCATGGTGGAG[C/T]ATGCCTGTAATCCCA | 105369632 |
rs782274549 | snp | C/G | | | | | GRCh38.p7 | 12:6891490 | GCGGAAACTAGGGCC[C/G]GAGGCTGAAAGTCCG | 105369632 |
rs782279884 | in-del | -/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886163 | GATTAAGTGCTGTGC[-/T]TTTAGATATGCATAC | 105369632 |
rs782284765 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877328 | GTCTGGAGGCAGAAT[G/T]AGAGGCCTGGGCTGG | 105369632 |
rs782287202 | snp | G/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875498 | GCTAATTTTTGTATT[G/T]TTAGTAGAGACAGGG | 105369632 |
rs782287566 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6875944 | AAGAGAGGAACATGG[A/T]CAGATAGGCATTTGA | 105369632 |
rs782288132 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876093 | CTCCTGAGTAGCTGG[A/G]ACTACAGGTGCATAC | 105369632 |
rs782291950 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882145 | GTTGTCTGTTCTTCA[A/G]TTTCATATAAATGGA | 105369632 |
rs782295296 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883611 | TAGGCATGCATTTTT[C/T]TTGGGTGCAAAACTA | 105369632 |
rs782295419 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878173 | TTTGGGAGGCCGAGG[C/G]AGGTGGATCACTTGA | 105369632 |
rs782297739 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884174 | GTAAGGTGCCCCATG[C/T]TGAGGCATCACTACA | 105369632 |
rs782302213 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889077 | GTGAGCCACCGTACC[A/G]CCGTTTTTTGTTTGT | 105369632 |
rs782302582 | snp | C/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883939 | GTGCACATGGCTGTG[C/G]GTGGTCCCTCAATTG | 105369632 |
rs782303287 | snp | G/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886224 | TATTGCTGCCCGCAG[G/T]TCCCACCTCCAGCCC | 105369632 |
rs782304836 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888824 | GACAGTCTCGCTCTG[C/T]AGCCGCGGCTGGAGT | 105369632 |
rs782307311 | snp | A/G | | | | | GRCh38.p7 | 12:6891792 | GGAGACACCCAGGTT[A/G]TGTTAGAAACTATGG | 105369632 |
rs782309029 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889526 | ATTATTAGTAGAGAC[A/G]GCATTTCACCATGTT | 105369632 |
rs782314534 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877767 | CCCAGGAGTTTGAGA[A/C]CAGCCTGGAAGACTA | 105369632 |
rs782320793 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879863 | TGTAATCCCACCACT[C/T]TGGGAGGCTGAGGCA | 105369632 |
rs782321935 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875601 | TGGGGTTACCGGCAT[A/G]AGCCACCGCGCCCAG | 105369632 |
rs782322279 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881626 | CTGGTGGGCTGAGGT[C/T]GGAGGACTGCTTGAG | 105369632 |
rs782328032 | snp | C/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886018 | AGCCTCTGAGTTCCC[C/T]TAGTATTTATTAATC | 105369632 |
rs782328540 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879201 | AACCAAACACCACCT[G/T]TTCCCCAATAACCTA | 105369632 |
rs782330534 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890446 | ATTTTCATTAACCAC[A/G]TATCTTCGTTGTCAC | 105369632 |
rs782334786 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887945 | TGAGCTGAGATCACA[A/C]CACTGCATTCCCGTC | 105369632 |
rs782335293 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876207 | TCTGTTGCCCAGGCT[A/G]GTCTCGAACTCCTGA | 105369632 |
rs782344544 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877204 | GAGTAATTGAGGGCA[C/G]GGGCAGGAGGGTGGG | 105369632 |
rs782344999 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888377 | TACAGGCGTGAGACA[C/T]CACACCTGGCCTCCC | 105369632 |
rs782345539 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876855 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 105369632 |
rs782351334 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879141 | CTGCTTGGGTGATGG[A/G]TGCACCAAAATCTCA | 105369632 |
rs782356556 | snp | C/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883206 | GATTACAGGCATGCG[C/G]CACCATGCCCAGCTA | 105369632 |
rs782357403 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882298 | TGTCTCTAAAAAAAA[A/G]AAAAAAGAAAGAAAG | 105369632 |
rs782357520 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884713 | CTACCCGCCCTCTCA[A/G]TCCCGCAGCCACGAG | 105369632 |
rs782366129 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880019 | GGAAGCCGAGGCAGA[A/C]GAACCACTTGAACCC | 105369632 |
rs782366480 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887612 | TTCCTCAATGATGTA[A/T]AAACAAAGCCATCAC | 105369632 |
rs782369601 | snp | C/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875671 | AGACGAGCCACTTCT[C/G]TGCAGTATGGAGGTT | 105369632 |
rs782369989 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881127 | CAGGCGCCCCGCCAG[C/T]ATGCCTGGATAATTT | 105369632 |
rs782370831 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880637 | AGTAATCCCCCCAAC[C/T]TCAGCCTCCCAAGTA | 105369632 |
rs782371028 | in-del | -/T/TTTT | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885354 | AAGTTAGGTGGATCC[-/T/TTTT]TTTTTTTTTTTTTTT | 105369632 |
rs782372628 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890759 | GGCTCAGAACTGGGA[A/C]CAAGAGAACATAGTC | 105369632 |
rs782377969 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881730 | AAAAACAAGGCCGGG[C/T]GCGGTGGCTCACGCC | 105369632 |
rs782382863 | snp | C/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883861 | GAAGAAGGCCTCTTG[C/G]CAGACCAGGATCTGT | 105369632 |
rs782389470 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884485 | GGAGAAAGCCAGAGT[C/T]ATCGCTGACTAGGAG | 105369632 |
rs782394318 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876542 | CCAGCTACTCAGGAG[C/G]TTGAGGCAGGAGAAT | 105369632 |
rs782394588 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884797 | GTGGTGGGCGAAGAT[A/G]ACCTGTTGTGCATCA | 105369632 |
rs782400390 | in-del | -/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881958 | GCAGTGAGCCGAGAT[-/C]GCGCCATTGCACTCC | 105369632 |
rs782400669 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886820 | TTTTGCTTTTCCCCA[C/T]ATATATCTAAAGTCT | 105369632 |
rs782404361 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880207 | AAGGTAAAAAATTTC[A/G]TAATGCTACAAGTAA | 105369632 |
rs782405822 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883567 | AAATTCCTTTTCAGA[A/G]AACTTTTTTCACAAG | 105369632 |
rs782406069 | snp | C/G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889713 | TCTCACCAATAGTTT[C/G/T]TGTGTTTTTGAGGTT | 105369632 |
rs782408367 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884726 | CAGTCCCGCAGCCAC[A/G]AGGAGGACGCTGCCC | 105369632 |
rs782410006 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887734 | GCACTTTAGGAGGCC[A/G]AGGTGGGTGTATCAG | 105369632 |
rs782415350 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891178 | CCCAGGTGCCAGTTG[C/G]GTAACCACGGCAAAG | 105369632 |
rs782420696 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881657 | GCTGCAGTGAGCCCT[A/G]ACCATGCCCACTGCA | 105369632 |
rs782422011 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890195 | GCAATGGTGCAATCT[C/T]GGCTCACTGCAACCT | 105369632 |
rs782428130 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885320 | GACCAGAAGATCTCA[A/G]TCGGGCTTGTACTGC | 105369632 |
rs782430706 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879608 | CTCCAGCCTGGGTGA[C/T]AGAGCGAGACCCCGT | 105369632 |
rs782435732 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880318 | GGGAGGCCGAGGCGG[A/G]TGGATCACAAGGTCA | 105369632 |
rs782440562 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884523 | TCCAGGCCTTGTTAG[C/T]CTCTGTATGGCCCAT | 105369632 |
rs782441498 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876793 | GATTTGGTGACTGAT[C/T]AGATATGGAGTTGAG | 105369632 |
rs782442219 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878292 | CCTATAATCCCAGCT[A/G]CGCAGGAGGCTGAGG | 105369632 |
rs782444795 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887174 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAGAAA | 105369632 |
rs782445365 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877010 | CAGGAGAATTGCTTG[-/A]ACCAGGGAGGTGGAG | 105369632 |
rs782448042 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881824 | CCTGGCTAACACGGT[A/G]AAACCCCGTCTCTAC | 105369632 |
rs782450801 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884157 | GGGCCCATCCACCCA[C/T]AGTAAGGTGCCCCAT | 105369632 |
rs782451370 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884899 | CAGAACTCTGAACAA[C/T]GTGCCTCAGGAGTGC | 105369632 |
rs782457763 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891289 | GAGTGCCTCGCGCGC[G/T]CCCCACAGCGGCCGC | 105369632 |
rs782458119 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881301 | AAAAGTCCCCTCCCA[C/T]CACTGCCGTTTTTAC | 105369632 |
rs782463062 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885618 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 105369632 |
rs782464044 | snp | G/T | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885683 | CTTTGAAGGATGCCC[G/T]GTGTAGATCATCATT | 105369632 |
rs782467636 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881196 | GCCCAGGTTGGTCTC[C/G]AACTCCTGGGCTCAA | 105369632 |
rs782467695 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884110 | CAGAAGCAAGGTGGC[C/T]AGCAAAAGCAGGCTG | 105369632 |
rs782471281 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886467 | ATATTTCAGACTATC[A/G]TATGGGGAGAAACCT | 105369632 |
rs782472209 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878821 | GAGCATATATTCGTT[G/T]GTGTAAAAATCACTA | 105369632 |
rs782472830 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882834 | TGTACAAGTCTGTTA[A/G]CAAAAGACCATGAGG | 105369632 |
rs782475595 | snp | C/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890289 | CCGTCACCACGCCCG[C/G]CTAATTTTTGCATTT | 105369632 |
rs782476250 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884268 | TGGCCCAGACCATTG[A/G]CATCTCTGAGGATGC | 105369632 |
rs782476637 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886411 | AACCTTTACGGGTGT[C/T]GGGATGGGGGATGGT | 105369632 |
rs782478050 | in-del | -/A | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884602 | TAGAAGAGGACGCTT[-/A]AAAAAAAAAAAAAAC | 105369632 |
rs782480305 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878540 | CAGATCACCTGAGGT[C/T]GGGAGTTTGAGGCCA | 105369632 |
rs782483507 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880551 | GCGACATTCCATCTC[-/A]AAAAAAAAAAAAAAA | 105369632 |
rs782490669 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887202 | AAAAGAAAAGAAAAG[-/A]AAAAAAATAAAGCCC | 105369632 |
rs782490919 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889252 | CTTGTGTTTCTAGTT[G/T]GGAAATATTAAATGC | 105369632 |
rs782492139 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876476 | ATGGAGAAACCCTGT[A/C]TCTACTAAAAATACA | 105369632 |
rs782493094 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875609 | CCGGCATGAGCCACC[A/G]CGCCCAGCCTGGGCT | 105369632 |
rs782498906 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889076 | TGTGAGCCACCGTAC[C/T]GCCGTTTTTTGTTTG | 105369632 |
rs782499335 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888171 | GCAGTAGCATGAGCA[C/T]GGCTCACTGCAGCCT | 105369632 |
rs782506752 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876458 | GAGACCAGCCTGGCC[A/C]ACATGGAGAAACCCT | 105369632 |
rs782509778 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879319 | TGCTTGCCAGTATGT[A/G]ACATCAATAATAACA | 105369632 |
rs782512719 | snp | A/T | | | | | GRCh38.p7 | 12:6891390 | TTTCCCCTGAACTGC[A/T]GCTTCCGTCCCCGCC | 105369632 |
rs782513139 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890650 | CTTTCAGATGGATCA[C/T]GTCATACAGAAAGGA | 105369632 |
rs782513642 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889080 | AGCCACCGTACCGCC[A/G]TTTTTTGTTTGTTTG | 105369632 |
rs782515919 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888216 | ACAGGTGATCCTCCT[A/G]CCTGCACCTCCTGAG | 105369632 |
rs782518485 | snp | A/G | | | | | GRCh38.p7 | 12:6892127 | AGTGCAGTGGCTTGA[A/G]CTTGGTTCACTGCAA | 105369632 |
rs782525538 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882516 | GACAGGAGTGCAGTC[A/G]TGCGATCTCGACTCA | 105369632 |
rs782525867 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889882 | TGCCATTGTAAGGCA[A/C]ATATTTCTTTTTGGT | 105369632 |
rs782527445 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881264 | TACAGGGGTGAGCCA[C/T]TGCGATCGGTCCTTT | 105369632 |
rs782534655 | snp | C/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875537 | TGTTGCCCAGGCTGG[C/T]CTCGAACTCCTGACC | 105369632 |
rs782542838 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890196 | CAATGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 105369632 |
rs782543470 | snp | C/G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878430 | CGACAGAGCAAGACT[C/G/T]CGTCTCAAAAAATAA | 105369632 |
rs782545122 | snp | A/C | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884008 | GGCAGGGCACCCAGC[A/C]GGAATGGCATGATCC | 105369632 |
rs782545333 | snp | C/T | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6875889 | GCAAATGTTTTCCCA[C/T]AGGACAGGCCAGTGA | 105369632 |
rs782550262 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882607 | GACTTCAGGCATGTA[C/T]TACAACGCCTGGATA | 105369632 |
rs782552295 | snp | G/T | | | | | GRCh38.p7 | 12:6891425 | TCTTCTCCGGCCCCA[G/T]CGCTGACTTTCATGC | 105369632 |
rs782558373 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879741 | GCCCCATGGCTAGCT[C/T]TAGCTCAGCTTGAGA | 105369632 |
rs782560428 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878708 | GTGAGCTGAGATTGA[A/G]CCATTGCACTCCAGC | 105369632 |
rs782571712 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890157 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAAG | 105369632 |
rs782573940 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6889174 | CCCCTGCACTTGGGG[C/G]CAAGGGCAAAGGGTG | 105369632 |
rs782576898 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887624 | GTATAAACAAAGCCA[C/T]CACGATCCACTTGCT | 105369632 |
rs782579179 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881499 | AGGCAGGGGATCACT[A/T]GAGCTCAAGAGTTCT | 105369632 |
rs782579477 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885297 | AAAACATGAATGGCA[A/G]ACAAACGGACCAGAA | 105369632 |
rs782591158 | in-del | -/AA | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876645 | TGAAACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 105369632 |
rs782594758 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888450 | GGACTTCCAGATCTT[A/T]ACCACATTAAGATTA | 105369632 |
rs782607505 | snp | C/T | | | | | GRCh38.p7 | 12:6891755 | ATCATTTTGTTCTCC[C/T]CGAGGAGGGAGGTCA | 105369632 |
rs782608227 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880459 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 105369632 |
rs782611294 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883971 | TCCCTCCTCTCTTTC[A/G]CTACCCCCTGGGCTG | 105369632 |
rs782611619 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879829 | ACATGGTTGTTGGCC[A/G]GGCACAGTGGCTCAC | 105369632 |
rs782616695 | snp | A/G | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885870 | ATATCTGTAGGGGTG[A/G]GTTGCCCCTCCACAC | 105369632 |
rs782619656 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878299 | TCCCAGCTACGCAGG[A/G]GGCTGAGGAAGGAGA | 105369632 |
rs782621369 | snp | G/T | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6889327 | GTATTCTGGAAGATG[G/T]CCTTTTCACCAGTAA | 105369632 |
rs782628452 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882158 | CAATTTCATATAAAT[G/T]GAATCATAATGTCAA | 105369632 |
rs782630105 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881563 | CTCTACTAAAAATTC[-/A]AAAAAGTTAGCTGGG | 105369632 |
rs782634842 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883677 | TATAGATTTAACCAC[A/G]TGCAATTTTCTGATT | 105369632 |
rs782638099 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883085 | TAGCCAATAATTTTT[G/T]TTTTCTGTTGCCCAG | 105369632 |
rs782642025 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887581 | ACCTGGCCAGGCCAA[C/G]AAGTTCTTTACTTTC | 105369632 |
rs782642469 | snp | A/C | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884258 | TACAAGAAGGTGGCC[A/C]AGACCATTGGCATCT | 105369632 |
rs782644348 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886578 | AGTGGTGATGACTCT[A/T]AAGGAGCATGCTGCC | 105369632 |
rs782646892 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888217 | CAGGTGATCCTCCTG[C/G]CTGCACCTCCTGAGT | 105369632 |
rs782652259 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884658 | CTTCGCGCTGGGTCT[C/G]TCGGTCCCGCAGCCA | 105369632 |
rs782654117 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885536 | TGTATTCTTAGTAGA[A/G]TCAGGGTTTCACCAT | 105369632 |
rs782657255 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880067 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGT | 105369632 |
rs782659262 | snp | A/C | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884697 | ACGCTGCCCAGACTC[A/C]CTACCCGCCCTCTCA | 105369632 |
rs782659853 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880578 | AAAAATTATAGATGA[A/G]GTCTTGCTATTTTGC | 105369632 |
rs782660241 | snp | A/C | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6882953 | TCACTGGAATAAAGT[A/C]TCTTCCCTCTGAATT | 105369632 |
rs782664219 | snp | A/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890510 | TTCACAAATTTTTTG[A/T]ATCTTGATTGAATGT | 105369632 |
rs782665154 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891094 | CGCCCAGCGCCAACG[C/T]TCCGTCCCGCCTCGC | 105369632 |
rs782667855 | snp | A/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883842 | CTGGGGCCTCTTCAT[A/T]GTCGAAGAAGGCCTC | 105369632 |
rs782670746 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888128 | TATTTATTGAGACAG[C/G]GTCTTGCTGTATCAC | 105369632 |
rs782672132 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891045 | AAATGACACAGCAAA[A/G]AATGTTTAAAACCAG | 105369632 |
rs782673081 | snp | C/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888561 | GATCAGCAGAGTGAA[C/G]GATGGAGTCATGTTG | 105369632 |
rs782673709 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889423 | GACTCACTGCAACCT[C/T]TGCCTCCTGGGTTCA | 105369632 |
rs782678305 | snp | C/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886028 | TTCCCTTAGTATTTA[C/T]TAATCATTTGTGGGT | 105369632 |
rs782681939 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877418 | GAGTGAAATATGGGC[A/G]ATGGGGACAAAGAGA | 105369632 |
rs782684525 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875518 | TAGAGACAGGGTTTC[A/G]CTATGTTGCCCAGGC | 105369632 |
rs782689509 | snp | A/C | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883000 | TCCCAGTATTTTGGG[A/C]AGCTGAGATGGGAAG | 105369632 |
rs782691354 | snp | G/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881130 | GCGCCCCGCCAGCAT[G/T]CCTGGATAATTTTTT | 105369632 |
rs782695871 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875371 | AAGCTCTGATGCCTA[A/G]GCTGGAGTGCAGTGG | 105369632 |
rs782696192 | snp | A/G | | | nc-transcript-variant | LOC105369632 | GRCh38.p7 | 12:6875777 | GGTTTGGGGAAGTAC[A/G]ATATCTTCAAGGTTG | 105369632 |
rs782697613 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884717 | CCGCCCTCTCAGTCC[C/T]GCAGCCACGAGGAGG | 105369632 |
rs782697944 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882310 | AAAGAAAAAAGAAAG[A/G]AAGAAAAAGAAAACA | 105369632 |
rs782703936 | snp | C/T | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886273 | TCTCAGTAGATGGAG[C/T]ATACAATCGGGTTTT | 105369632 |
rs782705990 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881877 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 105369632 |
rs782709204 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878636 | CATGCCTGTAATCCC[-/A]GCTACTCGGGAGGCT | 105369632 |
rs782710133 | snp | A/G | | | | | GRCh38.p7 | 12:6891804 | GTTGTGTTAGAAACT[A/G]TGGTAGCTGGGGCGA | 105369632 |
rs782710982 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6878330 | ATCGTGCCTGTAATC[C/T]CAGCTACTCAGGAGG | 105369632 |
rs782711941 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887181 | TCTGTCTCAAAAAAA[A/G]AAAAGAAAAGAAAAG | 105369632 |
rs782717320 | in-del | -/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876272 | ACTGGGATTACAGGC[-/G]TGAGCCACTGTGCCT | 105369632 |
rs782718782 | snp | C/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884354 | GAGGACCGCTCCTCA[C/T]TCATCCTCTTCCCCA | 105369632 |
rs782719389 | snp | C/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890096 | TTTCTGGTTTTTGTC[C/T]TTCGGTAATGTTTAG | 105369632 |
rs782721828 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887958 | CACCACTGCATTCCC[A/G]TCTGGGCAACAGAGC | 105369632 |
rs782727068 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881750 | TGGCTCACGCCTGTA[A/T]TCCCAGCACTTTGGG | 105369632 |
rs782727823 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879501 | GCTTTGGTGGCTTGC[A/G]CCTGCCATCCCAGCT | 105369632 |
rs782727989 | snp | A/G | | | intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6886082 | CAGGGTCACAAGACA[A/G]TTGTGGGGAGAGGGT | 105369632 |
rs782730369 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884539 | CTCTGTATGGCCCAT[A/G]CAAATGCCCAGCTCT | 105369632 |
rs782731553 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888000 | CAAAACACAAAAAAC[-/A]AAAAAAAAAAAAGAG | 105369632 |
rs782732927 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887077 | TACGAGGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 105369632 |
rs782739167 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890478 | TTAGCAGTTGTAGGA[G/T]AATCTGCTGACCTCG | 105369632 |
rs782741514 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6889753 | TTCTAAAATCATTAT[A/G]CCATCCTTGGCTGGT | 105369632 |
rs782747396 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879169 | TCACAAATCACCACG[A/G]AAGAACTTACTCATA | 105369632 |
rs782748433 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876944 | AAAATACAAAAATTA[A/G]CTGTGTGTGGTGGTG | 105369632 |
rs782754344 | snp | A/G | | | nc-transcript-variant, intron-variant | DSTNP2, LOC105369632 | GRCh38.p7 | 12:6885499 | GGGATTATAGCGTGC[A/G]CCACCACACCTGGCT | 105369632 |
rs782760911 | snp | C/T | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883773 | TCGGGCTCTGTCCAC[C/T]GCCATAGGCCTAGCA | 105369632 |
rs782761042 | snp | G/T | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891236 | GACTGTCGCCGGGCG[G/T]CGGTCACGTGAGCGG | 105369632 |
rs782763658 | snp | G/T | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884049 | CTTCCACAAGGACTG[G/T]CAGTGGTGTGGCCAT | 105369632 |
rs782765480 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886330 | ACAGGCAGGTGACAG[A/G]TGCCTTCCTCTTGTC | 105369632 |
rs782766752 | snp | G/T | | | | | GRCh38.p7 | 12:6891853 | CCAGCTACTCAGGAG[G/T]CTAGGGCAGGAGGAT | 105369632 |
rs782768449 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882567 | GTTCAAGCAATTCTC[A/G]TGCTTCAACCTCCTA | 105369632 |
rs782775905 | snp | A/G | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875678 | CCACTTCTCTGCAGT[A/G]TGGAGGTTGGGTTAC | 105369632 |
rs782779091 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876461 | ACCAGCCTGGCCAAC[A/G]TGGAGAAACCCTGTC | 105369632 |
rs782785928 | snp | A/C | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890246 | ATACTCTTGCCTCAG[A/C]CTCCTGAGTAGCTGG | 105369632 |
rs782789483 | snp | C/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887720 | CGCCTGTAATCCCAG[C/T]ACTTTAGGAGGCCGA | 105369632 |
rs782789622 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6888976 | TTTAATAGAGATGGG[A/G]TTTCACTGTGTTGGC | 105369632 |
rs782790525 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6879257 | AGAAGAAAGCATACT[A/G]AAATAAAGATATGAA | 105369632 |
rs782792395 | snp | C/T | | | downstream-variant-500B | LOC105369632 | GRCh38.p7 | 12:6875610 | CGGCATGAGCCACCG[C/T]GCCCAGCCTGGGCTG | 105369632 |
rs782792579 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6891177 | GCCCAGGTGCCAGTT[A/G]CGTAACCACGGCAAA | 105369632 |
rs782794330 | snp | A/G | | | upstream-variant-2KB | LOC105369632 | GRCh38.p7 | 12:6890577 | TTTGGGGATAGACTT[A/G]TATGCTAGCATGGAA | 105369632 |
rs782798838 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6880245 | TTTTACTTAAAAATT[-/A]AAAAAAAAAAAAAAA | 105369632 |
rs782800536 | snp | A/G | | | nc-transcript-variant, upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884522 | TTCCAGGCCTTGTTA[A/G]TCTCTGTATGGCCCA | 105369632 |
rs782804448 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6884754 | CCCAGACTCACTACC[C/T]GCCGGCTCCCTCCCC | 105369632 |
rs782809287 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6881677 | TGCCCACTGCACTCC[A/G]GCCTGAGTGACAGAG | 105369632 |
rs782813636 | snp | A/C | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6876312 | TGCATTTTAGAAAAA[A/C]CACCCTGGCAGCAAC | 105369632 |
rs782817344 | snp | A/G | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6877034 | GGTGGAGGCTGCAGT[A/G]AGCCGAGATGGCGCT | 105369632 |
rs782818435 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, DSTNP2, LOC105369632 | GRCh38.p7 | 12:6883323 | GCCTCCCAAAGTGCT[A/G]GGATTATAGGCATGA | 105369632 |
rs782818724 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6882512 | CCCAGACAGGAGTGC[A/G]GTCGTGCGATCTCGA | 105369632 |
rs782819845 | snp | A/T | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6886849 | CTAAAGTTGTTTTTT[A/T]AAAAAAAAAAAAGAA | 105369632 |
rs796420990 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | RPL13P5, LOC105369632 | GRCh38.p7 | 12:6881988 | CAGCCTGGGTGACAG[-/AG]CAAGACTCCATCTCA | 105369632 |
rs796924787 | in-del | -/A | | | intron-variant | LOC105369632 | GRCh38.p7 | 12:6887260 | TAATGCAAAAAAAAA[-/A]TTATTCAGACATTTT | 105369632 |
rs186706423 | snp | C/T | | | | | | : | TGTCTGGGCCAGGTG[C/T]AAGTGGCTCAGGCCT | 105369632 |