SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs36717 | snp | C/T | 0.25045 | 0.25 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460241 | GTTGGAGTGCAGTGG[C/T]GCCATCACGGCTCAC | 58513 |
rs36718 | snp | C/T | 0.234692 | 0.249531 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457480 | TGGCAAGCCTGTCTC[C/T]GGCACTGCTTTGGTG | 58513 |
rs36719 | snp | G/T | 0.234109 | 0.249494 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456956 | GGCACCCCCTCCCCA[G/T]GTTCTGCTTGCCCTG | 58513 |
rs36720 | snp | A/G | 0.4776 | 0.103433 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456540 | cctcccaagtagctg[A/G]gattacaggtacccg | 58513 |
rs36721 | snp | A/G | 0.239326 | 0.249772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455090 | CCAGGCTGGAGTGCA[A/G]TGATGTGATCCTGGC | 58513 |
rs40171 | snp | G/T | 0.234109 | 0.249494 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457435 | CCTCGCTTGACTGAG[G/T]CTCCCTGGACAGGCT | 58513 |
rs658931 | snp | A/G | 0.477684 | 0.103247 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452897 | aggcaggagaatggc[A/G]tgaaccggggaggcg | 58513 |
rs748262 | snp | A/G | 0.2462 | 0.249971 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376384 | TGGGATTTCTCTCGT[A/G]TGACAGAGTTAGGCC | 58513 |
rs873636 | snp | A/G | 0.471281 | 0.11634 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403960 | TAAAAGATGTTAAAG[A/G]GATTCACAGTGCAGG | 58513 |
rs875622 | snp | C/T | 0.442249 | 0.159814 | intron-variant, synonymous-codon, missense | EPS15L1 | GRCh38.p7 | 19:16356948 | GCTGGTCAGAGGCAG[C/T]GCATCGCAGAGAGAC | 58513 |
rs875623 | snp | C/T | 0.348134 | 0.229934 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357192 | ACAGCGGGCCCACCC[C/T]CAGGTTGTCACGCAG | 58513 |
rs882306 | snp | C/T | 0.249886 | 0.25 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381337 | GTCTGGTGGCCCCAG[C/T]CTGGGAGGCAGACGA | 58513 |
rs897791 | snp | C/T | 0.242775 | 0.249896 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380048 | ACTAGACACTGGAGC[C/T]TTAGCTGGCTGCATC | 58513 |
rs921940 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445011 | GGCATGAGCCACCAC[A/G]CCCAGCCCCAGGCGA | 58513 |
rs936312 | snp | A/G | 0.244776 | 0.249945 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435316 | TAGGAATAGCTCTTC[A/G]TGAACAGAGGGAAGG | 58513 |
rs936313 | snp | A/G | 0.244776 | 0.249945 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435573 | CAAGACAGAGCCCTC[A/G]GTCACAGAGATGAGA | 58513 |
rs1003113 | snp | G/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406783 | ATTTGCCCAGAAGAG[G/T]CATGACAGGAGGACA | 58513 |
rs1009904 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399112 | CCCCTGCACTGACAG[C/T]CAGGCCTGCAATCAC | 58513 |
rs1017690 | snp | G/T | 0.208779 | 0.246578 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422246 | GAGGTGACCGGGCCC[G/T]GGTTGACCCATGATG | 58513 |
rs1060791 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355380 | CCCAGGGCTTCCCCG[A/C]CTCCTCCCTACTCAT | 58513 |
rs1107955 | snp | A/G | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378427 | CCTGCTGGGGAACTC[A/G]GCCCACCTCGTCCAC | 58513 |
rs1107956 | snp | C/G | 0.126909 | 0.217598 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378437 | AACTCGGCCCACCTC[C/G]TCCACCAGGAACCCC | 58513 |
rs1551561 | snp | A/G | 0.0581099 | 0.160244 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402024 | GGGCCAACCACCCAA[A/G]TTCAGAGGGCTTCTC | 58513 |
rs1870071 | snp | A/G | 0.47709 | 0.104548 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394295 | GGGAAGAGAGGAGTG[A/G]ATTCTAGCCCACTCT | 58513 |
rs2034892 | snp | C/T | 0.479095 | 0.100076 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380738 | CTAAATTGTAGAGAC[C/T]TAGAGAGTCGCATCT | 58513 |
rs2124915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417728 | TGTACTAAAGGGACA[A/G]TTTTATCCCTGGGCC | 58513 |
rs2168647 | snp | C/T | 0.327211 | 0.237778 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375018 | ACATGCTCTCATAGA[C/T]AACAGCTGGGCATGC | 58513 |
rs2290666 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394396 | TCATTGCTGCAGGGC[C/T]GGTGATAAAGTGAGG | 58513 |
rs2290667 | snp | G/T | 0.0170715 | 0.0907983 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394043 | CCCGGCCCGCATCCT[G/T]TGCCCTAGAGCTAAT | 58513 |
rs2290668 | snp | C/T | 0.484632 | 0.086302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385981 | TCCCCTTCCTGGGCA[C/T]GCGCTGGCATCTTTC | 58513 |
rs2290669 | snp | G/T | 0.450231 | 0.149691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384963 | TGTGATCCAATGCAC[G/T]GCAGTCCCGTGGGGT | 58513 |
rs2305781 | snp | A/G | 0.207559 | 0.246371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442103 | AAAGGCCGCTCAGCC[A/G]GGCTTCTATTCTGTA | 58513 |
rs2362468 | snp | A/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376054 | TCCAGGGGAGGGGCA[A/C]GTGTAGGCAGGAGGG | 58513 |
rs2363120 | snp | A/C | 0.493925 | 0.054776 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409060 | GACCCTGTCTCTTAA[A/C]AAAAAAAAATTGTTT | 58513 |
rs2363121 | snp | C/T | 0.206947 | 0.246265 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441199 | ACAGGCGTGAACCAC[C/T]GCGCTTGGCCACTTG | 58513 |
rs2607278 | snp | C/T | 0.47709 | 0.104548 | | | GRCh38.p7 | 19:16457386 | CATACACCCAGGGCA[C/T]CAGGAGACCTGGAAG | 58513 |
rs2885706 | snp | A/C | 0.478271 | 0.101943 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472126 | CAGGGGCGGGGCCGC[A/C]CACACGCAGCCTGGA | 58513 |
rs3082716 | in-del | -/TG | 0.491525 | 0.0645418 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375467 | GTGATTATGCATATA[-/TG]TGTGTGTGTGTGTGT | 58513 |
rs3745315 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383852 | GGCAGCCAAGGGAGA[C/T]TGCCCAGTCACACTG | 58513 |
rs3745316 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383906 | GGCCGGTGGGGCCCC[A/G]AGGGGGCCTCATGCC | 58513 |
rs3786578 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363460 | CACACAGGCCAGCCT[C/T]GGTCCCTCTCCATGC | 58513 |
rs3786579 | snp | A/G | 0.209084 | 0.246629 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364747 | TGTGAGCCCCAGGCT[A/G]TCCACTGGAGCAGAA | 58513 |
rs3786580 | snp | A/G | 0.294832 | 0.245947 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364762 | GTCCACTGGAGCAGA[A/G]GGGGCTCCCTAGGGC | 58513 |
rs3786581 | snp | C/G | 0.293551 | 0.246177 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364815 | GCGAGGGCCCCTCAC[C/G]TCCACCCTCCCGTCC | 58513 |
rs3786582 | snp | C/G | 0.207559 | 0.246371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374723 | CTGTTGAGTGGGATG[C/G]CTCCTCCTCAGGGCC | 58513 |
rs3786584 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375304 | CAGGTGCATGCATGC[A/C]TGTGTCTGCAGGCGT | 58513 |
rs3786585 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377837 | CATGCCCGGCCACCC[A/G]CACTGGTCAGCATGC | 58513 |
rs3786586 | snp | A/G | 0.209693 | 0.246729 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384476 | GATGTTCCCTGTTGA[A/G]TTCTCTATGCTACCT | 58513 |
rs3786587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392168 | TGGGATACCAGCTCC[C/T]GGAGAACAGACACCA | 58513 |
rs3786588 | snp | C/T | 0.208169 | 0.246476 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405932 | AGCTGCCATGTGGAG[C/T]GTGGTGCAAGGGGCC | 58513 |
rs3786589 | snp | A/G | 0.236434 | 0.249632 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415976 | CGGCCCCCAGGAGCT[A/G]AGACAGAACAGGAAC | 58513 |
rs4399660 | snp | A/G | 0.214843 | 0.247516 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443717 | CTCTGTCTCAAAAAT[A/G]AAAAGAAAAAAATAA | 58513 |
rs4470265 | snp | A/G | 0.170408 | 0.236992 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469089 | GCAAGTAGGAAGTAG[A/G]ATGGCCCAGACCACT | 58513 |
rs4545941 | snp | C/T | 0.155987 | 0.23165 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423396 | CACAGCAAGACCCCA[C/T]CTCTACAAAATAAAT | 58513 |
rs4808047 | snp | C/T | 0.381503 | 0.21262 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417023 | CCGCTCCTCGCCATC[C/T]GAGACCCAATTGCCC | 58513 |
rs4808496 | snp | A/T | 0.243919 | 0.249926 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359866 | AGACTCATCTCCAAA[A/T]ATGTAAAAACCAAAA | 58513 |
rs4808497 | snp | A/C | 0.257732 | 0.24988 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359900 | TAGGGAAAAAAAAAA[A/C]AAAAACAGAAAACAA | 58513 |
rs4808498 | snp | C/T | 0.249603 | 0.25 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369260 | CAAGCAGCACAGCCC[C/T]GGGAGATAAGAATCT | 58513 |
rs4808500 | snp | C/T | 0.152667 | 0.230274 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389126 | agAaatcgcttgaac[C/T]tgggaggcggaggtt | 58513 |
rs4808501 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392648 | aatgacagaagtgtt[C/T]tCAAATTGCACACAA | 58513 |
rs4808502 | snp | A/C | 0.322721 | 0.23919 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393048 | ccccatctctaaata[A/C]ataaataaaaTATCC | 58513 |
rs4808503 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420853 | ACTGACAGGGTCTCC[C/T]TGTGCTCACCCTCCC | 58513 |
rs4808504 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420917 | GGGCCTCCTGCCCCC[A/G]CCCTCACCCTGCCAG | 58513 |
rs4808505 | snp | C/T | 0.14665 | 0.227637 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427766 | GGCTGTGATGGAGTG[C/T]ACCTGTAATTCCAGC | 58513 |
rs4808508 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428532 | GAAAGTGAAAGAAAG[A/G]AAGGAAGAAAGACAG | 58513 |
rs4808509 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428536 | GTGAAAGAAAGAAAG[A/G]AAGAAAGACAGAAAA | 58513 |
rs4808510 | snp | A/C | 0.479824 | 0.098392 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428545 | AGAAAGGAAGAAAGA[A/C]AGAAAAGAAAGGAAA | 58513 |
rs4808511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447500 | cactctggctcacac[C/T]tgtaatcccagcact | 58513 |
rs4808513 | snp | C/G | 0.478104 | 0.102316 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469687 | AGTGCAGACAGGAGT[C/G]GGGGTGGAGAAAACA | 58513 |
rs5827337 | in-del | -/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399682 | TTTTGCTTTTTGGGG[-/T]TTTTTTTTTTTTTTT | 58513 |
rs6512105 | snp | A/T | 0.227074 | 0.248947 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367986 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 58513 |
rs6512106 | snp | A/T | 0.2462 | 0.249971 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368211 | CTCATCCTACACAAC[A/T]GTGGACACACATACA | 58513 |
rs6512107 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385525 | GTCAGGAGGCGAGGA[A/G]CAACTCCAGGGCGAC | 58513 |
rs7245590 | snp | C/T | 0.238171 | 0.24972 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399468 | CTTAGGAAATACACA[C/T]GGCAACTCTGAAAGG | 58513 |
rs7247807 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452526 | tcgagaagctaaggc[A/G]ggaggattgcctgag | 58513 |
rs7250165 | snp | G/T | 0.242775 | 0.249896 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379784 | TCACACCAGTGCAGA[G/T]GTCTAAGGCTCCAGT | 58513 |
rs7251346 | snp | A/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417902 | CCTGGTGGCAGGCGG[A/T]GGGAAGGGATGTCAA | 58513 |
rs7251554 | snp | A/C | 0.242775 | 0.249896 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379783 | GTCACACCAGTGCAG[A/C]GGTCTAAGGCTCCAG | 58513 |
rs7251806 | snp | C/T | 0.397994 | 0.201489 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388758 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 58513 |
rs7252649 | snp | G/T | 0.268422 | 0.24932 | utr-variant-5-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16471974 | CGGGCTCCGAGCGCC[G/T]GGGGAACGGGGGCGG | 58513 |
rs7253951 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449998 | gggataaggaagaga[A/T]gggctgggagggaag | 58513 |
rs7255877 | snp | C/T | 0.25045 | 0.25 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468384 | TGAGTCTCACCCTGT[C/T]GCCCAGGCTGGGGTG | 58513 |
rs7256705 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464268 | AGCTGGGACTCCTAT[A/G]AAGGGAAAAGCCCAA | 58513 |
rs7256818 | snp | A/C | 0.47802 | 0.102502 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447955 | CAGACACACACAGAT[A/C]TGCCCAGTGGATTTC | 58513 |
rs7258646 | snp | C/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373176 | CCTATGGGTCCTTCA[C/G]ACTTTTTGTCAGTCT | 58513 |
rs7260337 | snp | C/T | 0.130694 | 0.219696 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390022 | tagacttaaaccata[C/T]caataattacattaa | 58513 |
rs7359963 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457356 | ATGGAGGGCCAGTCC[A/G]CAGCCAGCAGCAGAC | 58513 |
rs7508550 | snp | A/C | 0.210605 | 0.246877 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393705 | taaaataaataaata[A/C]atTAGCAAGCAATGT | 58513 |
rs8100142 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385789 | TCTACACTGTGAGAT[A/G]AGGTTCCTTCAAACA | 58513 |
rs8100152 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370158 | CAGAGCCCACCAGGA[A/G]CTCCCATGGTGGGGG | 58513 |
rs8100479 | snp | A/G | 0.148661 | 0.22854 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360904 | ATCTATAAATAACAC[A/G]TCTCACACCTAATGA | 58513 |
rs8101713 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394354 | TGCCAGCTCCCTGGG[C/T]AAGAGGACACAGGAC | 58513 |
rs8102323 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397382 | ggcgtgagccaccgc[A/G]cccggctgtttgtct | 58513 |
rs8102735 | snp | A/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390478 | aaacaagacacagat[A/T]atctgaacactatga | 58513 |
rs8103474 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397239 | ggattacaggcgtgc[A/G]ccaccatgcccagct | 58513 |
rs8106973 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362694 | tttgtatttttagta[A/G]agatgggattttgcc | 58513 |
rs8109484 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438428 | AAATTTCAGATGCAT[A/G]TATTTTCCAAAAACT | 58513 |
rs8110761 | snp | A/G | 0.474903 | 0.109173 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390194 | gaaaaatgatgtatc[A/G]tgtagtgaataacat | 58513 |
rs8111949 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393656 | tccgtctcaaaaaaa[A/T]aaaaaataaaaaata | 58513 |
rs8113380 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390426 | ggagaatgtttaacg[C/T]ctctctctcagacac | 58513 |
rs8113386 | snp | C/G | 0.499575 | 0.0145705 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361060 | ACTCCTTGAAGCGAC[C/G]GCATGTTACAATCTG | 58513 |
rs10221451 | snp | C/T | 0.17332 | 0.23795 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464120 | TATGTCAGCCTGACC[C/T]GCAGGCAGTCAGTAA | 58513 |
rs10221523 | snp | A/G | 0.039522 | 0.134904 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463788 | ACCAGTGGTAACAGA[A/G]ATGCTGGGCCAGTTT | 58513 |
rs10401133 | snp | C/T | 0.176219 | 0.238865 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463697 | ACCTAGTCTAGGTGG[C/T]TGGGGAAGACAGACC | 58513 |
rs10401355 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457867 | GTCACCCAAGACTGG[G/T]GGGGAGGGGGGAACA | 58513 |
rs10402422 | snp | A/G | 0.47666 | 0.105476 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364577 | CCCCCACCTTGAGAC[A/G]GCCTCCCATGCAGGG | 58513 |
rs10403387 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400331 | gacagagcgagactc[C/G]gtctcaaaaaaaaaa | 58513 |
rs10403555 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355348 | GCGTGGGAGGGCGGG[C/T]GGGGATGTCTGCAGC | 58513 |
rs10404046 | snp | C/G | 0.475348 | 0.108251 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366444 | GCGGTTAAGAATTCT[C/G]CCTGCTACCATTTCA | 58513 |
rs10404125 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358052 | CTGACAGTAATGTTC[A/G]CCTGGATCCAAATCA | 58513 |
rs10404237 | snp | A/C | 0.341909 | 0.232492 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400360 | AAAAACAAAAACAAA[A/C]AAAAAAAAAAACCCC | 58513 |
rs10408945 | snp | G/T | 0.226188 | 0.248863 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466180 | TTTAGTAGAGACAGG[G/T]TTTCAGCATGTTGGC | 58513 |
rs10410427 | snp | A/G | 0.207559 | 0.246371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445174 | TGAGCAACAAGATCC[A/G]CAACCAAGAGAAACA | 58513 |
rs10411058 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409837 | cagctacttgggagg[C/T]taaggcaggagaatc | 58513 |
rs10411344 | snp | A/C | 0.212122 | 0.247114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409592 | tgagaaggtatttgc[A/C]agtcacatatctgac | 58513 |
rs10411785 | snp | A/C | 0.212728 | 0.247206 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459102 | ATCTAAACATATCTA[A/C]ACATAGCAAAGGCAC | 58513 |
rs10411936 | snp | A/G | 0.47614 | 0.106587 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437564 | AGCTAGACAGAGGTA[A/G]TGAAGACACAACACT | 58513 |
rs10412060 | snp | C/T | 0.200492 | 0.245049 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468070 | TGAGCCCAGTTACCA[C/T]GCGCTTCCTAGGTAC | 58513 |
rs10412455 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453285 | ctattttttattttt[C/T]gtagagacggggtct | 58513 |
rs10412460 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358693 | GCCCCGGGAGGCGCC[C/T]GGCACCTGTCCTCAC | 58513 |
rs10413853 | snp | A/G | 0.271972 | 0.249033 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396329 | tgcagttgcacactc[A/G]tgggttactccagcc | 58513 |
rs10414546 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362794 | ggattacaggcatga[A/G]ccactgcacctggcc | 58513 |
rs10414740 | snp | G/T | 0.0729998 | 0.176553 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450785 | accacgcctggccAG[G/T]GCATGTCCAACTTCT | 58513 |
rs10415269 | snp | A/C | 0.00441499 | 0.0467761 | utr-variant-5-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16471953 | GCCGCCATCTTCCCG[A/C]GGACTCGGGCTCCGA | 58513 |
rs10419156 | snp | C/T | 0.206029 | 0.246103 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438859 | AGTCGTAAATACACA[C/T]GGTTGGTCAGAAACT | 58513 |
rs10421112 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414580 | taatttttgtatttt[C/T]agtagagacggggtt | 58513 |
rs10421164 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393606 | gtgagccgagatcgc[A/G]ccactgcactccagc | 58513 |
rs10421234 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368828 | GGTGATCCCACACAA[A/C]CACAACTGTCATTCA | 58513 |
rs10421252 | snp | C/T | 0.208779 | 0.246578 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368849 | CTGTCATTCATCCTA[C/T]ACAACACAGATGCCC | 58513 |
rs10422048 | snp | A/G | 0.207559 | 0.246371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368805 | ACTGTCATTCACCCT[A/G]CACAACAGGTGATCC | 58513 |
rs10423142 | snp | C/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372855 | TTCCTCCAATGTCCA[C/G]AAACCAGCCTGATCA | 58513 |
rs10423248 | snp | A/G | 0.219349 | 0.248114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460700 | GCACGGGGGTGCCGC[A/G]GGCACAGAGCGTTCT | 58513 |
rs10423953 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381627 | CAAGTACGAAGCTGC[A/G]ATTGGAATCTGGGAG | 58513 |
rs10424066 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373264 | CTTCCTCCTCACTCA[A/G]CCACGCTGGGACCCA | 58513 |
rs10424196 | snp | A/G | 0.17654 | 0.238964 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461161 | atacaaaaattagcc[A/G]ggcgtggtggcaggc | 58513 |
rs10424717 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452279 | ggtgaaaccccatct[C/T]tactaaaaatataaa | 58513 |
rs10425235 | snp | A/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452153 | caaaaaaaaaaaaCC[A/C]CACAACAGGAggctg | 58513 |
rs10425541 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403290 | TAGAGAATGGGGGTC[C/T]TGCATGGCGTGATGC | 58513 |
rs10518278 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464487 | GACACAAACTCTCAC[A/G]TCTTATTTACCAAAA | 58513 |
rs10543332 | in-del | -/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369677 | CTGGAAGAAAAAAAA[-/GT]GTGTGTGTGTGTGTG | 58513 |
rs10570713 | in-del | -/GTGT | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472404 | GTTCCTAGGATCGCA[-/GTGT]gtgtgtgtgtgtgtg | 58513 |
rs10612334 | in-del | -/AGC | 0.077417 | 0.180873 | intron-variant, cds-indel | EPS15L1 | GRCh38.p7 | 19:16401333 | AAAAGAAACACATCA[-/AGC]ATTGAACATAAAGAG | 58513 |
rs10665196 | in-del | -/GAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428550 | GAAGAAAGACAGAAA[-/GAAA]AGAAAGGAAAAGAAA | 58513 |
rs11086030 | snp | C/T | 0.282346 | 0.247899 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377094 | GGCACCGGTAGGCGG[C/T]GGCTGCGAGAGAAGA | 58513 |
rs11271210 | in-del | -/AAGAGGACACAGGACCCTGGGC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394376 | GCCAGCTCCCTGGGT[-/AAGAGGACACAGGACCCTGGGC]AAGAGGACACAGGAC | 58513 |
rs11289907 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453887 | AAAAAGAATTCCTAT[-/A]AAAAAAAAAAAAAGG | 58513 |
rs11344510 | in-del | -/A | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373482 | TTGGACTTTATGCTT[-/A]AAAAAAAAAAAAAAA | 58513 |
rs11413626 | in-del | -/A/AA | 0 | 0 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361270 | TTTAAAAAAAAAAAA[-/A/AA]CTTCAAATTGCTCTT | 58513 |
rs11666733 | snp | A/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367275 | CGGCAGTGAATAAAG[A/C]CAAATGAAATTAAAG | 58513 |
rs11666784 | snp | A/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367352 | CAGGGGGCAAGGGAT[A/C]CAAGACTGAAGAAAA | 58513 |
rs11667613 | snp | A/C | 0.00468381 | 0.0481661 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367483 | ACCAAATGGTTTACC[A/C]CAGTATGTGCTGTTA | 58513 |
rs11878217 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400208 | tgggcatggtggcac[A/G]tgcctgtaatctctg | 58513 |
rs11878602 | snp | A/C | 0.49607 | 0.0441545 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444342 | AGCAACAGCAGCCCC[A/C]AGATGGCTGCCCCCC | 58513 |
rs11879699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460213 | aggatgaacccagga[G/T]tctgaggctgcagtg | 58513 |
rs11881209 | snp | A/C | 0.00952359 | 0.0683454 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403487 | CCCACCCCACCCCGC[A/C]TACTCCTTGAAGATG | 58513 |
rs11882196 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450730 | tcaggtgatccaccc[A/G]cctcagcctcccaaa | 58513 |
rs12052197 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452243 | ctgaggtcaggagtt[C/T]taaaccagcctggcc | 58513 |
rs12459106 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457640 | AACTGGAATGGCGCC[C/G]GGGCAGGAGGGGAAC | 58513 |
rs12459477 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390584 | gtttgttcaccaaca[C/T]aggccacaaacaaca | 58513 |
rs12459821 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419048 | cccccacaactaagc[A/G]tcccctgcccacata | 58513 |
rs12459886 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373607 | TTCACCCGACACTCA[C/T]CTGCTGACCGCTCTT | 58513 |
rs12460131 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406709 | CCTCCTTTACCTCCT[C/T]CTCAAACCAAAGATG | 58513 |
rs12460183 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472065 | GGGAGAGGGCGGGGC[C/T]GTAGACAGGGCCACG | 58513 |
rs12460440 | snp | C/G | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359748 | GCGCCTGAGGTCCCA[C/G]CTACGTGGGAGGCTG | 58513 |
rs12460648 | snp | C/T | 0.257454 | 0.249889 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455183 | AGTGCAGTGGCACGA[C/T]CATAGCTCACTGTAG | 58513 |
rs12460667 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442747 | GACCAGCCCGCGCCC[A/G]GAGAGCGCTGGCCAG | 58513 |
rs12460699 | snp | C/T | 0.47709 | 0.104548 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433241 | caaacgattctcctg[C/T]ctcagcctcccaagt | 58513 |
rs12461349 | snp | C/T | 0.211819 | 0.247067 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385697 | AGCTGCAGGACCAAG[C/T]GGGGCCTGTTCCCAA | 58513 |
rs12461547 | snp | A/C | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387782 | aacaaacaaaaaaaa[A/C]CCCCACTTCATTAGG | 58513 |
rs12461692 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470406 | AAAAAAAAATTGGAC[A/G]GGAAGTTTTAGAAAG | 58513 |
rs12461829 | snp | G/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400054 | TTAAGAACCCTGACT[G/T]TGGCGGGTGAGGTGG | 58513 |
rs12462102 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432866 | ggagtgccatggcac[A/G]atctcagcttattgc | 58513 |
rs12462331 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368295 | CTACACAACAGTGGA[C/T]GCACACATACAACCA | 58513 |
rs12462600 | snp | A/G | 0.148996 | 0.228688 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469234 | TCCAGGGGAGGGAGC[A/G]CACAGAGAGATAAGA | 58513 |
rs12462717 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419487 | AAAAATGAGGAGCCA[A/G]CCAGGAAGGGAAGGG | 58513 |
rs12462740 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419626 | GGCAGAAGCCATTAC[A/G]ACAGAAGTTTCCCCT | 58513 |
rs12608539 | snp | C/G | 0.247621 | 0.249989 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387607 | agtgaaactccgttt[C/G]aaaaataaataagcc | 58513 |
rs12609018 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389112 | tacaaaaattaaccA[A/G]Aaatcgcttgaactt | 58513 |
rs12609019 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409718 | caaggtgggaggatc[A/C]cctgaggtcaggagt | 58513 |
rs12610582 | snp | G/T | 0.00376647 | 0.0432325 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398089 | AAAGAAAGTTTCCTA[G/T]CAAGGCTGCCACCAC | 58513 |
rs12611408 | snp | A/G | 0.433527 | 0.169758 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464877 | TCACAAGGTCAGATC[A/G]AGACCATCCTGCCTA | 58513 |
rs12971448 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406056 | GAGGAGGGGTGGGTT[G/T]GCGGGGAGCCATGGC | 58513 |
rs12972932 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464909 | ccagtgaaaccccgt[A/C]tctactaaaaataca | 58513 |
rs12972942 | snp | A/G | 0.492037 | 0.0625946 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466836 | tgaatccaggaggca[A/G]aggttgcagtgagcc | 58513 |
rs12974924 | snp | C/T | 0.015624 | 0.0869937 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451265 | cAGACTCTCCAACAA[C/T]TGCAAGTGAGTCTAC | 58513 |
rs12977042 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405959 | GGCCATCAGGACGCA[G/T]GAACTGCAGGGGCCT | 58513 |
rs12977090 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404002 | CTCCGAGAAAGAACT[C/T]TTAGCCCCCATCCCC | 58513 |
rs12977117 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404026 | CATCCCCGAAACAAG[C/T]TAAGCCAGGGACGCA | 58513 |
rs12977264 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405994 | TGGGGTCCAGGGAGA[A/G]GCAGCAGCAGCTGGG | 58513 |
rs12977779 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397028 | tgtgaatatacctaa[A/C]actactgaactgtac | 58513 |
rs12977831 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403966 | ATGTTAAAGAGATTC[A/C]CAGTGCAGGATGAAA | 58513 |
rs12978240 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412556 | tggcttacacctata[A/C]tcctaacactttgag | 58513 |
rs12978252 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412564 | acctataatcctaac[A/C]ctttgagaagccaag | 58513 |
rs12978922 | snp | A/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405957 | GGGGCCATCAGGACG[A/C]AGGAACTGCAGGGGC | 58513 |
rs12978948 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405985 | GGCCTCGGGTGGGGT[A/C]CAGGGAGAGGCAGCA | 58513 |
rs12980044 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405993 | GTGGGGTCCAGGGAG[A/C]GGCAGCAGCAGCTGG | 58513 |
rs12980683 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450592 | ttcaagtgattctcc[A/T]gcctcagcctcccaa | 58513 |
rs12982140 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393655 | ctccgtctcaaaaaa[A/T]aaaaaaataaaaaat | 58513 |
rs12982399 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409771 | ggtgaaaccctgtct[C/T]tactaaaaacacaaa | 58513 |
rs12982907 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452031 | gtaatcccagttact[C/T]tggaggctgaggcag | 58513 |
rs12984756 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412554 | ggtggcttacaccta[A/T]aatcctaacactttg | 58513 |
rs12986037 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362542 | tttttttttttttca[A/G]agacagagtcttgct | 58513 |
rs12986042 | snp | G/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472023 | GCACTGGGACGACGG[G/T]AGGGCGGTGCGCAGG | 58513 |
rs12986341 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405984 | GGGCCTCGGGTGGGG[G/T]CCAGGGAGAGGCAGC | 58513 |
rs13344661 | snp | A/T | 0.19334 | 0.243495 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397696 | TTTGCATTTTTTTTT[A/T]AAAGTGTGTATTTCT | 58513 |
rs13353278 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374453 | CTGAACCCTGAAGCC[A/G]GGCCCAAGGAAGTCA | 58513 |
rs16981267 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430774 | GGATGCAAGTGCGCA[C/T]GGATGAATGTATAAA | 58513 |
rs16981270 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436719 | CAACTCCCAATTCCA[A/G]TGAAGGGCCACAGCC | 58513 |
rs16981271 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442354 | TGCACTTTAAACATC[C/T]TCTGAACACAGAATT | 58513 |
rs16995422 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408234 | GGAGCTCAGAGCAAA[A/G]AGAAGACAAAAATAA | 58513 |
rs17642703 | snp | A/G | 0.209388 | 0.246679 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436158 | CCATGACCTCTCCAA[A/G]AAGGGAGCAAACCAA | 58513 |
rs17642764 | snp | C/T | 0.214843 | 0.247516 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445810 | CCAGGGGATGAGGCC[C/T]GCACCGTAAGAGGCT | 58513 |
rs17709809 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400652 | TTAAAAACTGTATTT[G/T]TACAACAGGATAAAA | 58513 |
rs17709957 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436796 | GGCCACTCACACTGA[A/G]ACAGAAGAGCTGACA | 58513 |
rs17723343 | snp | A/T | 0.0908922 | 0.192833 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383458 | GCCACCGTGTGGCCA[A/T]CGTTTTCTGCTTTCG | 58513 |
rs17723444 | snp | C/T | 0.150667 | 0.229419 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406563 | CCCATCACCGGGTAA[C/T]GCTGGCAGCAACTCC | 58513 |
rs17723516 | snp | A/G | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423015 | CAGTGTTGACAACCC[A/G]AAGATGTCCATAGGA | 58513 |
rs17723565 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436507 | GAAAGAATGGTAACA[C/T]GCAAAGTGGCTGGAA | 58513 |
rs17723614 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446945 | CAGGAAGTTAGGCAT[A/G]TAACACTGAAACACA | 58513 |
rs17796498 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421081 | GGGAGCACTTAAGAC[A/G]GACCAGAGGCCCTTC | 58513 |
rs17796594 | snp | A/G | 0.078151 | 0.181571 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445929 | GAAGACGCCATCTTC[A/G]CCTCTGCAGTGTGTG | 58513 |
rs28365816 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395323 | TCACTTGCTACCCAC[C/T]TTCTCATTGAAAGAC | 58513 |
rs28494886 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428566 | AGAAAGGAAAAGAAA[A/G]GAAAAGGAAAGGAAA | 58513 |
rs28505051 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367782 | AAAAAACCCAAAAAA[A/C]AACAAACAAACAAAA | 58513 |
rs28521356 | snp | A/G | 0.210301 | 0.246828 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473495 | CCTAGGTGACAGAGC[A/G]AGACTCTGTCTAAAA | 58513 |
rs28536652 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441445 | CTACTGCACTCCAGC[C/G]TGGGCGACAGAGCGA | 58513 |
rs28580247 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439697 | CTCAAAAAATAAAAA[A/T]TAAAAAAACAAAACA | 58513 |
rs28627028 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439698 | TCAAAAAATAAAAAA[A/T]AAAAAAACAAAACAA | 58513 |
rs28654474 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473571 | CTGAGTATAAAAGTG[C/T]TGGAAGTACTGGAAG | 58513 |
rs28697894 | snp | A/C | 0.209084 | 0.246629 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408530 | CTGGGTGTGGGGGCA[A/C]GCATCTGCATTCTCA | 58513 |
rs28774999 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469257 | AGATAAGATGCAGGT[A/G]GGGAGGCTGAAATTA | 58513 |
rs28881609 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414706 | GCCTGGCCTTTTTTT[G/T]GTTTTGTTTTTTTTT | 58513 |
rs33914440 | snp | C/T | 0.0953193 | 0.196408 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436967 | GGCCTCTGCAGAGGG[C/T]GGTGTGACCATCAGA | 58513 |
rs34086602 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407708 | ACAATTGTTTAAACC[-/T]TGCTGGGTAATTTTT | 58513 |
rs34099100 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374883 | ATATGTGTGTGCACG[-/T]TTTGCATGCATGCAT | 58513 |
rs34105711 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365716 | CCCTCCACGGGAAAG[-/C]CCCCCCCTCCCCCAG | 58513 |
rs34129551 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422980 | TCGGGGAAAAAAAAA[-/G]GGGGGGGGGGATTTC | 58513 |
rs34160022 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460543 | AAGAAAATGCCAACT[-/C]CCATGGCCTGGTGTG | 58513 |
rs34205589 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448767 | CCAGCGGGCAGAGGC[-/T]TGCAGTGAGCCGAGA | 58513 |
rs34293191 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440561 | CTATTTGTGCAACTT[-/C]CCACGAGAGACTGGT | 58513 |
rs34324108 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371567 | AATAATCATTAAATT[-/G]GGGGAGAGGTTAAAG | 58513 |
rs34427922 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434809 | GGCAGTGTCTTTGCA[-/G]GGGAGACAAAGATCA | 58513 |
rs34482179 | in-del | -/A | 0.153997 | 0.230832 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470219 | CCACTAAAAAAAAAA[-/A]TACAAAAATTAGCCG | 58513 |
rs34503524 | in-del | -/A | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440067 | TTAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs34524974 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458936 | TCGTCGTGAGGACAT[-/A]CCTGGAGTGAACTTA | 58513 |
rs34567084 | in-del | -/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361414 | GTAACTTTCGCAATC[-/T]TTCTTTTCATACTTC | 58513 |
rs34568915 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445106 | AAAAAAGAGTTTCAG[-/T]TCTTTGAGGCATGCA | 58513 |
rs34575569 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470785 | GCTGCGGTCTCTACT[-/C]CCCAAACGTCCAAAT | 58513 |
rs34606533 | in-del | -/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402724 | GGCAACAAACCAAGA[-/C]CCCATCTCTGCAAAA | 58513 |
rs34677927 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435219 | GCCTCCCAAAGTGCT[-/G]GGGATTACAGGTGTG | 58513 |
rs34693413 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410029 | TCCCAGCTACTCGGG[-/A]AAGCCGAGGCACGAA | 58513 |
rs34735773 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462044 | CCTCGACCCTCCCGG[-/T]AGCCCATGGTGTGGC | 58513 |
rs34773317 | in-del | -/G | 0.464947 | 0.127663 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455313 | TTTTTTGTAAAGATT[-/G]GGGGGGTCTCATTAT | 58513 |
rs34782743 | in-del | -/T | 0.249038 | 0.249998 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402547 | TGTCAGAAAAGACGC[-/T]TTTTTTTTTTAAAAC | 58513 |
rs34870847 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447222 | CATCAGGGAAACGCT[-/G]GGGGTATGTCTAACC | 58513 |
rs34886434 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374152 | CCTGCTGCCACCTTG[-/C]CTGTGTGACCTTGGG | 58513 |
rs34926762 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408769 | TTCAAAACTTTTACA[-/G]GGGCTGCAGTAATCA | 58513 |
rs34957020 | snp | A/C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357271 | GCTCACACTCTAGAC[A/C/T]TTTTCCCCCCCAGGC | 58513 |
rs34971290 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417279 | GCCCACGACCTGCCT[-/G]GGGACCACACAGCTG | 58513 |
rs34992990 | in-del | -/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361596 | GCTCTTTTTTTTTTT[-/T]ATTGAGAAACTGTTT | 58513 |
rs34999809 | in-del | -/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402093 | AGGTTCTGAAAGGAT[-/C]CCAGGCCTATCTTGG | 58513 |
rs35042571 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368600 | CACACAACAGGTGGT[A/G]CCCACACAACCATCA | 58513 |
rs35184990 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363502 | GCCTTTCCCTCTGTT[-/C]CCCCAGCAGATCAGC | 58513 |
rs35185027 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458882 | CATCGTTTAACTACA[-/G]GGGATGCGTCCTGAG | 58513 |
rs35225493 | snp | A/T | 0.0722614 | 0.17581 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419337 | GGTGGCGCGCGCCTG[A/T]AATCCCAGCTGCTCA | 58513 |
rs35243922 | snp | C/T | 0.00256794 | 0.0357404 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404711 | AGCCTCGAGCTCCTG[C/T]AAACTGCTTGTTTCC | 58513 |
rs35304655 | in-del | -/A | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356236 | AGACAATTCTGCACT[-/A]CTGGGAATGTGGTAT | 58513 |
rs35345542 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404749 | GGTCATTTTGTAATT[-/C]CTAGGGAGGAGTTGC | 58513 |
rs35371205 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371150 | TCAACAAAAGGTTTT[-/G]GGGACCCACATGGGC | 58513 |
rs35373143 | snp | G/T | 0.466086 | 0.125726 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399921 | ACCTTTCTTAATCTG[G/T]CCTCAGTAAGGCCTA | 58513 |
rs35410965 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373698 | AAGGGAATTGTACAG[-/T]AGCCCGGCTCTGATT | 58513 |
rs35415397 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434154 | GGATTCTGGCACCTT[-/C]CCCCAGGGACTGGGT | 58513 |
rs35546786 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458897 | GGGATGCGTCCTGAG[-/T]AGTTGCATCGTCAGG | 58513 |
rs35560400 | snp | A/G | 0.027392 | 0.113779 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425259 | GTGGGATGAGGGACG[A/G]GGGCAGGGCGGAGGG | 58513 |
rs35579731 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428066 | TGAGGTGGGCATAGT[-/G]GGCAGGTGCCTGTAA | 58513 |
rs35582141 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422782 | GCCAACATGGTGAAA[-/C]CCCCTCTCTACTAAA | 58513 |
rs35618195 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441382 | AGGCTGAGGCAGGAG[-/T]AATGGCGTGAACCCA | 58513 |
rs35730661 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402704 | GTGTCACCACCTATA[-/T]TTTTGGGCAACAAAC | 58513 |
rs35743635 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360590 | TACAAAAAAAAAAAA[-/A]TTAAACATTAGCCTT | 58513 |
rs35752272 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429925 | ATGCCGTGCACTGCA[-/G]GGGTGGTGAGCAGCA | 58513 |
rs35756709 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377666 | GGTGCTTGGCACATG[-/C]CCCTGGTGTGCCGCC | 58513 |
rs35810631 | snp | A/G | 0.408163 | 0.193609 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421363 | GCCCGAGTGCATGAA[A/G]ATCTCCTTCACCTCC | 58513 |
rs35820633 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462182 | CTAGAAACAAGCACA[-/G]GGGACAATGGCACCA | 58513 |
rs35920637 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428987 | ATGATTATAATCATA[C/T]TGATTATAAGATTAT | 58513 |
rs35931531 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371172 | ACATGGGCACATGAT[-/G]GGGGAGAGGTCACTG | 58513 |
rs36048519 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445664 | GACCTCTTGGCCCCC[-/A]AAAGGAAGATTCACA | 58513 |
rs36099927 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368664 | TCACCCTACACAACA[-/G]GGCGATCTCACAAAA | 58513 |
rs41278192 | snp | A/G | 0.0495569 | 0.149407 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404569 | ATAGGGCGCTGCCCC[A/G]GAGGTGGCCGGGACC | 58513 |
rs55637134 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397419 | CCTGAAAGTTAAACA[A/G]TTTTTTTTTAATCAA | 58513 |
rs55701241 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363386 | GGCTCCCAGCCACAC[C/T]TGCCCCGCCCACCAC | 58513 |
rs55712949 | snp | A/G | 0.0399052 | 0.1355 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355633 | ACGGTGTGTGTGTGT[A/G]TATATAGACATCTGC | 58513 |
rs55738447 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385536 | AGGAGCAACTCCAGG[-/G]CGACCTGCCACCCAC | 58513 |
rs55834724 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380525 | CACACACGCAGCCAT[C/T]TAAGGCTCTAGCGTC | 58513 |
rs55842081 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434954 | TTTTTTTTTTTTTTC[C/T]TTTTTTGAGACAAAA | 58513 |
rs55922737 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423601 | AAAAAATCTATGGAT[C/T]TAATTCAAATGATGA | 58513 |
rs56061532 | snp | G/T | 0.244776 | 0.249945 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439079 | TTTTTTTTCTGTTTT[G/T]TTTTTTTTTTATTAA | 58513 |
rs56075425 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434067 | TGGGGAGCTTAAGAC[G/T]GAGCTCTACTGGTCC | 58513 |
rs56244514 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393673 | AAAAATAAAAAATAA[A/T]TAAATAAATAAATAA | 58513 |
rs56249051 | in-del | -/TGTG | 0 | 0 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472431 | GTGTGTGTGTGTGTG[-/TGTG]CGCGCTAATTTGGGG | 58513 |
rs56250700 | in-del | -/CACTAA/CACTAACACTAA | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464772 | TAACACTAACACTAA[-/CACTAA/CACTAACACTAA]TGATAGCTGATGAGC | 58513 |
rs56319940 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434953 | TTTTTTTTTTTTTTT[C/T]TTTTTTTGAGACAAA | 58513 |
rs56330833 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393662 | TCAAAAAAAAAAAAA[A/T]TAAAAAATAAATAAA | 58513 |
rs56397532 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416175 | GTTAATATGACCCCC[A/G]GGGATCCCCCAGCTA | 58513 |
rs56407399 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379320 | AAAAATAAAAAAAAT[-/T]AAAAAAGATCATGTG | 58513 |
rs56824066 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448556 | AAAAAAGGGGGGGGG[-/G]AGAAAGGCCGGGCGC | 58513 |
rs56856203 | snp | C/T | 0.00164377 | 0.0286214 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425320 | CAAGTGCATGGCCTG[C/T]AGGTGCAAACAACAA | 58513 |
rs56900530 | in-del | -/AATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433997 | ATAAATAAATAAATA[-/AATA]GACACAGACACACAT | 58513 |
rs57143961 | in-del | -/T | 0.320335 | 0.239902 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422414 | CTTCCCTTTTTTTTT[-/T]AAATATTTACACAAA | 58513 |
rs57153030 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357506 | GATTGGCAGCGTCTG[C/G]ATATTTCACGGCTTG | 58513 |
rs57213610 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375013 | GGTGTGCATGCCCAG[C/T]TGTTATCTATGAGAG | 58513 |
rs57277477 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391638 | TTTTTTTTTTTTTTT[-/T]GGTTTTGAAATCCAA | 58513 |
rs57357644 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377510 | AGTCCCATACCTCCA[C/T]GGGCTTCTAGCACCA | 58513 |
rs57370131 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396687 | ACGGAAAAACAAAAT[G/T]TTTTTCTAAGTCAGA | 58513 |
rs57617764 | snp | A/T | 0.247621 | 0.249989 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419463 | CTCTGTCTCAAAAAA[A/T]AAAAATAAAAAAATG | 58513 |
rs57685681 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419635 | CATTACAACAGAAGT[C/T]TCCCCTTTTACCAAA | 58513 |
rs57839742 | snp | A/G | 0.447291 | 0.153545 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448557 | AAAAAAGGGGGGGGG[A/G]GAAAGGCCGGGCGCG | 58513 |
rs58052449 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438233 | TGGCAGGTGCCTGAA[A/C]TCCCAGCTACTTGGG | 58513 |
rs58135052 | snp | A/G | 0.239902 | 0.249796 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424099 | GCTCAGCAGCCACAG[A/G]TCCCAAAGGAAGGAT | 58513 |
rs58166386 | snp | A/G | 0.479177 | 0.0998894 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448610 | GCACATTGGGAGGCC[A/G]AGGTAGGCGGATCAC | 58513 |
rs58200356 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450102 | AAAAAAAAAAAATAG[C/T]CACGCATGGTGGCAC | 58513 |
rs58224667 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452651 | AAAAAAAAAAAAAAA[-/A]CCTAAGAACTAAAAA | 58513 |
rs58270062 | in-del | -/GGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412724 | GGGGTGGGGGGGGGG[-/GGGG]TGTCAGAGGCCCTGG | 58513 |
rs58287978 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465094 | AAAAAAAAAAAAAAA[-/A]TTCACAAGAAAACCT | 58513 |
rs58399321 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432830 | TTTTTTAAACAGAGT[A/C]TCAATCCGGTTGCCC | 58513 |
rs58478203 | snp | C/T | 0.141596 | 0.225274 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473724 | AGCACTTTGGGAGGC[C/T]GAGGTGGATGGATCA | 58513 |
rs58598075 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409247 | AAACAAATTTTTTAA[A/G]GTAAAATAATAAAAA | 58513 |
rs58813814 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430596 | ATAAGTCTCAGCCTC[A/T]TAGCTATTACTTATT | 58513 |
rs58979854 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469353 | GCGGAGTTCGAGGAG[G/T]ATCGGCTGCAGCCAC | 58513 |
rs58992224 | snp | A/C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395936 | GGCGATAGAGTGAGT[A/C/G]TATCTCAAAAAAAAA | 58513 |
rs59028060 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430594 | AAATAAGTCTCAGCC[A/T]CTTAGCTATTACTTA | 58513 |
rs59033629 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373826 | CCACTGGGTCAACTC[A/G]GTGTTTGGACTGTTA | 58513 |
rs59155277 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465124 | TCATAATGTTTTAGG[A/G]AAGTTTACAAATTTG | 58513 |
rs59326120 | snp | C/T | 0.39709 | 0.20215 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393541 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 58513 |
rs59329828 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424736 | CGCGCTCTCAGCTCA[C/T]TGCAACCTCCGTCTC | 58513 |
rs59600386 | in-del | -/G | 0.239902 | 0.249796 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422971 | TCGGGGAAAAAAAAA[-/G]GGGGGGGGGATTTCT | 58513 |
rs59600532 | snp | A/G | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404641 | TCAGCATGTCTCGGA[A/G]CTTGGCCTTCTGCTG | 58513 |
rs59619467 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363719 | AGGAGTCTCCTCCCA[C/T]TCAGTGTCCTGCACC | 58513 |
rs59682235 | in-del | -/AGATTA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395936 | GCGATAGAGTGAGTC[-/AGATTA]TATCTCAAAAAAAAA | 58513 |
rs59825837 | snp | C/T | 0.245916 | 0.249967 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432634 | AAAATTAGCCGGCTG[C/T]TGTGGTGCATGCCTG | 58513 |
rs59869950 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448938 | AAATATATACTAGAG[A/C]GCTCTCAAATTCAAC | 58513 |
rs59903814 | snp | A/G | 0.128288 | 0.218372 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362469 | TTCGGTGTGTTAGTT[A/G]TAAGGGTCTGCACAC | 58513 |
rs59915356 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396803 | TTCTGACACATGCTC[C/T]AACATGGAAGAACCT | 58513 |
rs60231018 | snp | A/G | 0.23846 | 0.249734 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419332 | GGCATGGTGGCGCGC[A/G]CCTGTAATCCCAGCT | 58513 |
rs60365066 | snp | A/G | 0.237593 | 0.249692 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412778 | TCCACGGAGGTTTCA[A/G]CAGTGGCATCTGGGG | 58513 |
rs60434491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413084 | GGCGTTTGTTGCTAT[C/T]GGGGACTACAATGGC | 58513 |
rs60454283 | in-del | -/AA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412518 | AAAAAGAAAAAAAAA[-/AA]TCTTCACTCTCGCCA | 58513 |
rs60524006 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437654 | GAATTTCACCACAAT[A/G]AAAGGGGAAGGCTAG | 58513 |
rs60689307 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367754 | AAAAAAAAAAAAAAA[-/A]CCCAAAAAACAACAA | 58513 |
rs60720757 | in-del | -/GT/GTGG/GTGTGG/GTGTGT/GTGTGTGTGTGTGTGTGT/GTTT/TA/TTGT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369708 | TGTGTGTGTGTGTGT[lengthTooLong]AGGGTGGGGTATGTG | 58513 |
rs60751956 | snp | C/T | 0.0130675 | 0.0797683 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425362 | GGGCAAGGCTGGGGC[C/T]GGGACCATCAGGAGA | 58513 |
rs60857071 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432066 | GTATGATAGGGGCCC[G/T]GGAACCAATCCCCCT | 58513 |
rs61110114 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398249 | ATGCACCCACATCCC[G/T]GCCATCTGATGAACA | 58513 |
rs61254358 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412647 | AATATATATATATAT[-/A]TTTTTAAAAACTTCT | 58513 |
rs61341481 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444058 | GACGGTGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 58513 |
rs61347144 | in-del | -/AA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444184 | GTCAAAAAAAAAAAA[-/AA]GAGGAAAAGAAAGGG | 58513 |
rs61537143 | snp | C/T | 0.225597 | 0.248806 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464811 | ATTCACGGGTGGGCA[C/T]GGTGGCTCACGCCTG | 58513 |
rs62118095 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365642 | CTGTGGGTTTGCAGG[A/G]GATAGGGACAGTGAC | 58513 |
rs62118096 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407134 | CATGGTGTGCTGTTA[C/T]GGCAAGCCAAATGGA | 58513 |
rs62118097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414034 | AGGACCTGTGACCAT[A/G]GGAGGGATCGCTCCC | 58513 |
rs62118098 | snp | C/T | 0.155656 | 0.231515 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414520 | ATTCTCCTGCCTCAG[C/T]CTCCCTAGTAGCTGG | 58513 |
rs62118099 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421876 | CCACATGCCAGCCTC[C/T]CTGGTCCTCCCACTC | 58513 |
rs62118100 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422412 | CGTGCTTTTCCTCTT[C/T]CCTTTTTTTTTAAAT | 58513 |
rs62118101 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425416 | GCTGCAGTGACAGGA[A/C]ACTCTGTCAGGACGC | 58513 |
rs62118102 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437118 | GGAAGACTTCACAAA[A/G]TTAAACACAGAATCA | 58513 |
rs62118103 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439220 | GAAGCCCTTGCAGAG[C/T]GTAGAGGATCATAAG | 58513 |
rs62118104 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453902 | AAAAAAAAAAAAAAG[A/G]CCATTTGATGTGCTT | 58513 |
rs62118105 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456657 | GAGTGAAACTCCATC[A/T]CAAAACAAAAACAAA | 58513 |
rs62118106 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471237 | CAGCACCTGACCCAA[C/G/T]GCACATTTGAGGGAT | 58513 |
rs62945060 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453900 | ATAAAAAAAAAAAAA[A/G]GGCCATTTGATGTGC | 58513 |
rs68004226 | in-del | -/A/AA | 0.271972 | 0.249033 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361258 | TTTAAAAAAAAAAAA[-/A/AA]CTTCAAATTGCTCTT | 58513 |
rs70950303 | multinucleotide-polymorphism | AG/CT | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379783 | GTCACACCAGTGCAG[AG/CT]GTCTAAGGCTCCAGT | 58513 |
rs71178690 | in-del | -/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362512 | TTTTTTTTTTTTTTT[-/T]CAGAGACAGAGTCTT | 58513 |
rs71178691 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367498 | CAGTATGTGCTGTTA[-/A]AAAAAAAAAAAAAAA | 58513 |
rs71178693 | in-del | -/GG | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412726 | GGTGGGGGGGGGGGG[-/GG]TGTCAGAGGCCCTGG | 58513 |
rs71178694 | in-del | -/AAGA/AATA | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428544 | AGAAAGGAAGAAAGA[-/AAGA/AATA]CAGAAAAGAAAGGAA | 58513 |
rs71334618 | in-del | -/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407348 | TCTCACTCTAACACC[-/C]AGGCTGGAGTGCAGC | 58513 |
rs71334619 | in-del | -/A | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452628 | ACATAGCAAAATGTC[-/A]ATCTGAAAAAAAAAA | 58513 |
rs71334620 | in-del | -/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452682 | ATACGTAGGTGGGGG[-/G]AAAAGATCAAAGGGT | 58513 |
rs71334621 | in-del | -/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468992 | ACCACTGCACTCCAG[-/C]CTGGGGGACAGAGCG | 58513 |
rs71336715 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367369 | AAGACTGAAGAAAAC[A/C/G]CAAAATAGAACTTAT | 58513 |
rs71336774 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367394 | ACTTATTTTCAAACC[A/C]CAGCAGTTTCAACAG | 58513 |
rs71336775 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367434 | CGGTGTACCGAAACC[A/C]CACACAGGACTGACT | 58513 |
rs71336776 | snp | C/T | 0.375 | 0.216506 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448752 | GGAGAACTGCTTGAA[C/T]CCAGCGGGCAGAGGC | 58513 |
rs71885683 | in-del | -/T | 0.34101 | 0.232846 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360065 | TTGAAACCTTGGGTG[-/T]TTTTTTTTTTTTTAT | 58513 |
rs72400077 | in-del | -/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369688 | AAAAGTGTGTGTGTG[-/TG]TGTGTGTGTGTGTGT | 58513 |
rs72479521 | snp | A/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417070 | CAAGGCCTTCCTAGC[A/T]CTGGGGAGGGGCTGA | 58513 |
rs73019098 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363351 | CTTGGATCTCTGGCT[A/G]CACCTCCAGAGAGCA | 58513 |
rs73021111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371225 | TGGCATTTCAGAGAA[A/G]TGGGAGAGCTGGCAG | 58513 |
rs73021131 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394911 | CTCTGGTTAACAGGG[A/T]GAGATAAGAAGCTTA | 58513 |
rs73021136 | snp | A/T | 0.0256867 | 0.110379 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402502 | TGTGCAACAAAGACA[A/T]CATCAGCATTAAGCA | 58513 |
rs73021138 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406470 | GGGGCACAGAGAGAG[A/C]CTGAGGTAGCCCAAT | 58513 |
rs73021141 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407820 | ATGTCATTGCTCCGT[C/T]AGGCCACAGCGCAGC | 58513 |
rs73021149 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419821 | TCCCCAGTCTGCCCC[C/T]GCGGGCCCCAGCCTG | 58513 |
rs73021155 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446317 | GGCCGAGGGCAGGAC[A/G]CCTCCTACATCTTCA | 58513 |
rs73509143 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366503 | GTTCAGAGAGATGAA[A/T]AGCTTCGTTCACACC | 58513 |
rs73509160 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380426 | CGTCTAGGCTTCTAG[C/T]GTTTACTCATACCAA | 58513 |
rs73509166 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382970 | TTTTTTGTTTTTTAA[A/G]AAAACACCTTCTTGC | 58513 |
rs73509167 | snp | C/T | 0.220246 | 0.248223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384730 | GAGAGTTCTGTCACA[C/T]GGGCGACTCTGAACA | 58513 |
rs73509175 | snp | A/G | 0.304438 | 0.244001 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391811 | AAGGCAGCCGGGCTG[A/G]GACGCCTGCACTTAC | 58513 |
rs73509177 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393219 | GCTGATTGGGATGGG[G/T]TCTCCTTTTGGGGGG | 58513 |
rs73509190 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401364 | AGGCAAGTGTGGTGT[C/T]TAGAGAGCACGAGCG | 58513 |
rs73509201 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407085 | CTCCTGAACTGTGAG[C/T]AGTAAACTTCTGTTG | 58513 |
rs73509202 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407211 | AGGGTACCTCACCAC[C/T]TCTCTAAGAGGGTTC | 58513 |
rs73511104 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407938 | ACTGTGTCTCCAAAC[C/T]CCTGAACTGAGGCAT | 58513 |
rs73511116 | snp | C/T | 0.00235866 | 0.0342603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413757 | TAGATGTAACCAAAA[C/T]GAACGAGACCCTTAC | 58513 |
rs73511120 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414127 | GATGTCCCAAGTGTG[A/G]TAAGGACCCAGAGCG | 58513 |
rs73511124 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420667 | ATTCTTTCCTTTTGA[C/T]AGCTCCCAAGTGAAG | 58513 |
rs73511126 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420788 | GTCGGCTGTGTCCAG[C/T]CCTGGGGGAAAGAGG | 58513 |
rs73511130 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422313 | GGGCAGGCCCCTTCC[A/G]TGGCCTACTCCACCT | 58513 |
rs73511134 | snp | C/T | 0.275464 | 0.2487 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426021 | ATGGTGGAACTCTCA[C/T]GGAAGAGTCTGAGAG | 58513 |
rs73511137 | snp | A/G | 0.210909 | 0.246925 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430251 | TCCACCACTGCCCTC[A/G]CTGGGCCAAACTGTG | 58513 |
rs73511139 | snp | A/G | 0.274929 | 0.248754 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430374 | TGCCCCGCCCTGTCC[A/G]CAGTAGGACCTCATC | 58513 |
rs73511140 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430455 | CTGAAGATCTGCTTC[A/G]CCATCTGAAAAATGG | 58513 |
rs73511162 | snp | C/T | 0.081446 | 0.184634 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445883 | GCAGAGCTGACCCGA[C/T]GTGTTCTCCTGACCC | 58513 |
rs73511172 | snp | A/C | 0.26818 | 0.249338 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449583 | GGCAGTTTCTTAAAA[A/C]AACAACAACAAAAAA | 58513 |
rs73511175 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452604 | TGGCTACTGCACTCC[G/T]GCCTGCACAACATAG | 58513 |
rs73511183 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458650 | CCCTGGCCATCTCCT[A/G]CCTTGCCGGGCTGAT | 58513 |
rs73511187 | snp | C/T | 0.160938 | 0.233598 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460318 | CACCAATTCTCTTAG[C/T]CTCAGCTGTCATTTT | 58513 |
rs73511188 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460625 | CCAGCCCATCAGCAA[C/T]TGTGGAGCCTGCTCC | 58513 |
rs73511192 | snp | A/C | 0.040671 | 0.13668 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464701 | CTTCCCTGGGCCACA[A/C]TAGAATTGTCTTGGG | 58513 |
rs73511194 | snp | C/T | 0.142947 | 0.22592 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466471 | TCATTTCTTTATATC[C/T]GGGCCCCTCCCAACG | 58513 |
rs73511195 | snp | A/C | 0.32885 | 0.23724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466611 | GTGATCTACAAAAGG[A/C]AGGCATGAGGGCCAG | 58513 |
rs73511201 | snp | C/T | 0.151001 | 0.229563 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469603 | GGTCAGAAAAGAGTA[C/T]ATAAGGAAGGAGATT | 58513 |
rs73511202 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469824 | AGCCACCTGCTGCAG[A/G]GTGCTTCCCTTTTGC | 58513 |
rs73513107 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470036 | ACGAAGAAAACCAGG[C/T]CACGCCTTCATTCAA | 58513 |
rs73513113 | snp | C/T | 0.141934 | 0.225437 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472657 | AAATAAATAAATAAA[C/T]AAGACAAGAACCCAC | 58513 |
rs73928603 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454372 | TCCTATCGCCCCGCT[A/G]CTGGAACCTGGCGGG | 58513 |
rs73928604 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458445 | TCCTGATGGGAGGGC[C/T]GCCCCGCCCCCACCC | 58513 |
rs73928605 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467822 | AACAGCAGGGCTCTG[C/T]GGCAGGAGGACGCAG | 58513 |
rs73928606 | snp | C/T | 0.021333 | 0.101051 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469449 | CTGGATGCATTTCCA[C/T]GGAAGGCTTTTTGGA | 58513 |
rs73931905 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367318 | GTGCTGACTGCCTAC[C/T]GCAGGGAGACTTCAT | 58513 |
rs73931906 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375200 | TGTGCCTGCATATGC[A/G]TACATGCAGGCACAT | 58513 |
rs73931907 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380353 | ATTTAAGGCTCTAGC[A/G]TCTAGTCACACAGAC | 58513 |
rs73931908 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380729 | TAGTCACACAGATGC[A/G]ACTCTCTAGGTCTCT | 58513 |
rs73931909 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391913 | GTGCAGGGTGGCCGG[A/G]TCCATGCGAGCATGT | 58513 |
rs73931910 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394860 | GGTCTTGTGGTGAGC[C/T]TGGAACACTTCCCAC | 58513 |
rs73931911 | snp | A/G | 0.0718919 | 0.175435 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401671 | CACACCTGTCTTGGT[A/G]TCAGGGGCTCAAGAG | 58513 |
rs73931912 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405399 | GTGAGTGTGGGAGGC[A/G]GGACATCATGATTCT | 58513 |
rs73931913 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408094 | GTTAGGCCGGATGGG[A/G]TAGCTCTGGACACCA | 58513 |
rs73931914 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413375 | CTACACCTCAGCCAG[A/G]GGCTGCACTGCCATC | 58513 |
rs73931915 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422273 | CCTCCTGGTTCAGAG[A/G]CATTGAGGCCCCTCA | 58513 |
rs73931916 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424308 | AATGCCGTCGTGGGG[A/G]CAGGAGCTATACCCT | 58513 |
rs73931917 | snp | C/T | 0.239902 | 0.249796 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426187 | AAGACATGTTGACAT[C/T]ACGTTCCCCCAGGTG | 58513 |
rs73931918 | snp | C/T | 0.239902 | 0.249796 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426195 | TTGACATCACGTTCC[C/T]CCAGGTGGGAGGCCC | 58513 |
rs73931919 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426847 | AGATAATAATAGACA[C/T]GCTCATACAGAATAT | 58513 |
rs74260252 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449993 | TGCCGGGGATAAGGA[A/G]GAGATGGGCTGGGAG | 58513 |
rs74260253 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450898 | ATATCCCAGATGCAA[C/T]ACTGTACCACCATTA | 58513 |
rs74260256 | snp | A/G | 0.141934 | 0.225437 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473052 | GGGCAACTTGAATCT[A/G]TGTCTCCTGGACTGC | 58513 |
rs74260257 | snp | A/G | 0.144296 | 0.226554 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473068 | TGTCTCCTGGACTGC[A/G]GTCCTCAACCTTGGC | 58513 |
rs74386081 | snp | C/G | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410535 | AAACAGGTGTTCACA[C/G]AAAAACTTGCAGACA | 58513 |
rs74394451 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401704 | CTCAAAAATGTAAGG[A/G]GCCGACAGTCCCCTG | 58513 |
rs74463730 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382218 | GCCTGGCACTGCCTC[C/T]GCAGTGAATCAGATC | 58513 |
rs74480758 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367937 | GGTCTCAATCAATCC[A/G]ATTAATAAAAATATT | 58513 |
rs74516259 | snp | G/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450496 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTC | 58513 |
rs74618372 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374646 | CGCCGGGTTTAGGTA[C/T]GTGGGGAGGCGGGGG | 58513 |
rs74736243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379961 | GTCTAGTCACATAGA[C/T]GCGGCTGTCTGAGGC | 58513 |
rs74806552 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457885 | GGAGGGGGGAACACC[A/G]AGAGGGGCTCAATGA | 58513 |
rs74808985 | snp | A/C/G | 0.0357906 | 0.129518 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404406 | CTTCTAGGAGTACAG[A/C/G]GGGGTGGCCAGGAAG | 58513 |
rs74850110 | snp | C/G | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408171 | TGGAGAAGGAGCCAT[C/G]AGAAAGTCCCAGAGG | 58513 |
rs74975453 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399698 | TTTTTTTTTTTTTTT[A/G]GAGATTGAGTCTCGC | 58513 |
rs74975891 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423842 | CTGTGGCGGGACACA[G/T]AAACAAGGGGGGTTC | 58513 |
rs74993164 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457748 | TGACCTGTGTCCCCT[A/G]GACATCACCCCTCCC | 58513 |
rs74998340 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466391 | CCTCCATCATCAGAT[C/T]GGAACCTGCCCTGCT | 58513 |
rs75038043 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439021 | CTAACCCAGGACCCA[C/T]CACACAAAGGCTCAG | 58513 |
rs75194941 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433456 | TTTAAAGAGAATGCA[C/T]AAAATTTTTCCTAAA | 58513 |
rs75299160 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365276 | AACAATTGTTCATAC[A/G]TTCAAGTCCTAACCC | 58513 |
rs75423168 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413614 | AGTGAATTCAGCCTG[A/G]AAAAAAAAAAAACAA | 58513 |
rs75449023 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450810 | ACTTCTGCTGGTCTC[A/G]CAAGGTGGTCATTTG | 58513 |
rs75460445 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393197 | CGGGAGGGAATGGGG[A/T]GTGACTGCTGATTGG | 58513 |
rs75514738 | snp | A/G | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419665 | AAGAGAGCTGGGACC[A/G]TTCTAACAGACTTAT | 58513 |
rs75549485 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435393 | ATAGGGCAGGCAGCC[C/T]GTAAAAGGGGCCATG | 58513 |
rs75669952 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419456 | AGTGAGTCTCTGTCT[A/C]AAAAAAAAAAAATAA | 58513 |
rs75720885 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469322 | TGAAGAGTGAAGACC[A/G]ACGGGCTCCAGTGTT | 58513 |
rs75738371 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419457 | GTGAGTCTCTGTCTC[A/C]AAAAAAAAAAATAAA | 58513 |
rs75766304 | snp | C/T | 0.237882 | 0.249706 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412000 | CACTACAGCCAGCCT[C/T]GTATACTTTAAATCA | 58513 |
rs75819996 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452216 | TTTGGGAGGCTGAGG[C/T]GGGTAGATCACCTGA | 58513 |
rs75879305 | snp | G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414728 | TTTTTTTTTTTTTTT[G/T]AGACAGGCTCTTGCT | 58513 |
rs75912298 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362546 | TTTTTTTTTCAGAGA[C/T]AGAGTCTTGCTCTGT | 58513 |
rs75992807 | snp | C/G | 0.00090051 | 0.0212001 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434512 | GGAAAGAAATAGCCC[C/G]AGTAAGTAGGAGAGC | 58513 |
rs76008369 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386672 | AAAGGAAGGGGAATC[A/G]GGATGGAGGGGCAGA | 58513 |
rs76032778 | snp | A/G | 0.236144 | 0.249616 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448297 | GCACTTTGGGAGGCC[A/G]AGGCAGGAGGATCAC | 58513 |
rs76056475 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403245 | GCCCCCCCCTGGACT[C/G]GGAAGAGGGTGGGGG | 58513 |
rs76056674 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423844 | GTGGCGGGACACAGA[A/C]ACAAGGGGGGTTCTG | 58513 |
rs76058628 | snp | G/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410042 | GGGAAGCCGAGGCAC[G/T]AAAATCATTTGAACC | 58513 |
rs76067775 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395793 | TACTAAAAATACAAA[A/C]AATTAGCTGGGTGTT | 58513 |
rs76102934 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408676 | AAAAAAAAAAAATCA[C/T]ATGGAAACACATGGG | 58513 |
rs76154324 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373239 | AGGCTCACAGGGGGT[C/G]GCATTTCACCTTCCT | 58513 |
rs76169076 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364788 | AGGGCTCCTGAGCAG[A/G]ATGGAGGGTGGGCGA | 58513 |
rs76169759 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356036 | CTGTCTCAGGCCCCC[A/C]ATCTGGAAAGCAGAG | 58513 |
rs76190744 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468848 | AAGACTTCATCTCTT[A/C]AAAAAAAAAATTGTT | 58513 |
rs76217516 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406887 | TTAGGTGTGGGGCCT[C/T]TAGGAGGTGATTAGG | 58513 |
rs76338861 | snp | C/T | 0.112631 | 0.208878 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423227 | TTCACGTAGCAAGTA[C/T]GTGTGATGAAGTACA | 58513 |
rs76359619 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465663 | CTCCAGCGTAGGCAA[C/T]AGAGCAAGAGCCTGT | 58513 |
rs76387153 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462379 | ATCAGGGAAGTGGGG[A/G]GGAGGGCATGGTGGC | 58513 |
rs76446608 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365270 | CCCCCCAACAATTGT[C/T]CATACGTTCAAGTCC | 58513 |
rs76457907 | in-del | -/TATAATAATAATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393077 | CCTGCAGGAGCTGGA[-/TATAATAATAATA]ATAATAATAATAATA | 58513 |
rs76495155 | snp | A/G | 0.105569 | 0.204058 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387904 | GAATGAAAAATAAAT[A/G]AATAAATAGAGCCTC | 58513 |
rs76546241 | snp | A/G | 0.000494185 | 0.0157114 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403851 | AATCGGTTCAGCTCC[A/G]ACTTGGCTCGGTTCA | 58513 |
rs76608830 | snp | A/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470229 | TCCACTAAAAAAAAA[A/T]TACAAAAATTAGCCG | 58513 |
rs76611404 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423846 | GGCGGGACACAGAAA[C/G]AAGGGGGGTTCTGTG | 58513 |
rs76619090 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459213 | TCCCTATGCTTGGGG[C/G]CGCTGCCTGCTGCAG | 58513 |
rs76626935 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470564 | TATTAACACCTATTA[C/T]CGGTAGGACACTTAA | 58513 |
rs76657124 | snp | A/G | 0.123452 | 0.215605 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460287 | TGTCTCTAAAAATAA[A/G]AAAAGAACAGTGTTT | 58513 |
rs76678562 | snp | A/G | 0.200182 | 0.244986 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472876 | GCTACTCAGGAGGCT[A/G]AGGCCAGAGAATCAC | 58513 |
rs76683546 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408725 | AACCCTGACAGAGAA[A/G]AAAAAGATGGAGGAT | 58513 |
rs76727641 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429410 | CTGGGCAGGCTGCCA[A/G]TCCCCGGATCTAAGC | 58513 |
rs76746645 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432004 | AGAGGGCCGACTTTT[G/T]TATGTGCAGGACTGA | 58513 |
rs76858078 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359898 | CTTAGGGAAAAAAAA[A/C]AAAAAAACAGAAAAC | 58513 |
rs76882237 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378571 | GAGCCACAGAGACAC[A/G]CTTCCAGGCCTCTCC | 58513 |
rs76898909 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365719 | CTCCACGGGAAAGCC[C/G]CCCCTCCCCCAGGGT | 58513 |
rs76935912 | snp | C/T | 0.108402 | 0.206034 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394417 | GCAGCAATGAGGCGG[C/T]GGCACCCCTGGGCTT | 58513 |
rs76975253 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363237 | CACCCCAGACTGGAA[A/G]CTCAATAATATGCAA | 58513 |
rs76985523 | snp | A/G | 0.00135119 | 0.0259571 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403871 | GGCTCGGTTCAGATC[A/G]TCTTCCTGGGACTTT | 58513 |
rs77031434 | snp | A/G | 0.197393 | 0.244402 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462034 | AAGACAGAGCTCCTC[A/G]ACCCTCCCGGAGCCC | 58513 |
rs77093067 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425560 | TCCAATCAAGCCAGA[C/T]TCCATATGCATCCCT | 58513 |
rs77108017 | snp | G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424678 | ATACTTTTTTTTTTT[G/T]AGATAGAGTTTCGCT | 58513 |
rs77110005 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403007 | GGTAAATCTCTGAGC[A/G]GTCCATGCTTGCGAT | 58513 |
rs77178026 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473775 | ACCAGCCTGGCCAAC[A/C]TGATGAAATCCCGTG | 58513 |
rs77200946 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399759 | GCAGCTGGCCTCAAG[C/G]AATCCTCCCACCTCA | 58513 |
rs77247410 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423847 | GCGGGACACAGAAAC[A/G]AGGGGGGTTCTGTGT | 58513 |
rs77285925 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441774 | AGGTCTGCAGCGACC[A/G]GGCCACTACCCAGGA | 58513 |
rs77300211 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367735 | GCTTAAAAGCATCCT[C/T]AAGAGCTGGGTGCAA | 58513 |
rs77302756 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359899 | TTAGGGAAAAAAAAA[A/C]AAAAAACAGAAAACA | 58513 |
rs77484426 | snp | A/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395960 | AAAAAAAAAAAAAAA[A/T]ATCAAGGTGTGGTGG | 58513 |
rs77582887 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458287 | ACCCCTCGAGGCTCC[C/T]GGACCCCACAGTGAG | 58513 |
rs77586934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382003 | TACCCTCTGTGTCGC[A/G]CAATAGGACCCGGGC | 58513 |
rs77600511 | snp | C/T | 0.108755 | 0.206276 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380006 | ACACCAATGCAGCTG[C/T]CTAAAGCTCCAGCAT | 58513 |
rs77624476 | snp | C/T | 0.210301 | 0.246828 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466859 | AGTGAGCCAAGACAG[C/T]GCCATTGCACTCCAT | 58513 |
rs77654591 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450479 | GCATGTCCATCTTCT[C/T]TTTTTTTTTTTTTTT | 58513 |
rs77682383 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375468 | TGATTATGCATATAT[A/G]TGTGTGTGTGTGTGT | 58513 |
rs77732836 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365193 | AGTGGCCCTGGAAGA[C/T]GGTGTGGGGCATGGC | 58513 |
rs77736475 | snp | C/G | 0.106278 | 0.204558 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458633 | CCAGTCCTGAAAGTG[C/G]TCCCTGGCCATCTCC | 58513 |
rs77739376 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368969 | CTGACATGTCTTATT[C/G]CACCCTCCCCATCCT | 58513 |
rs77739744 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403019 | AGCGGTCCATGCTTG[C/T]GATCAACTGTGGCCT | 58513 |
rs77903322 | snp | A/G | 0.102014 | 0.201495 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465073 | AACAGAGCGAGACTT[A/G]GTCTCAAAAAAAAAA | 58513 |
rs77925195 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372527 | CAACTCCCTGCACGC[C/T]TTTTTTAACGGAAAA | 58513 |
rs77930327 | snp | G/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403821 | CTCTGCTCCAGCTGG[G/T]TTTCCTCCTGCTGCA | 58513 |
rs77931469 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363903 | AGTCTTCCTTCCCAC[A/G]GTTTGCACAGAAGGA | 58513 |
rs78070767 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396778 | GATTCAGCCTTCAAA[A/G]GGAAGCAAATTCTGA | 58513 |
rs78087042 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416846 | TGAAGAGGATCCAGA[A/G]GGGAATACAGGAAGT | 58513 |
rs78132037 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426981 | GTTTTTAGGAAATAC[A/G]CACTGAAGTGTTTGT | 58513 |
rs78142814 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379445 | AGAGACAGAGAACAG[A/G]TCAAGAGTACAAAGG | 58513 |
rs78212608 | snp | A/T | 0.0807149 | 0.183963 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420543 | CACCTCACAGTGTGG[A/T]CATCTGTGAATTACC | 58513 |
rs78449992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410626 | AAAATGTGGCCCATC[A/G]TGGCTTGGCATGGTG | 58513 |
rs78481157 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410222 | AATGATTTTTCTCCA[A/G]TGACTACATACAAAT | 58513 |
rs78625996 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359344 | CCACCAGCTGATCGG[C/T]TGAGCCCCCGAATGC | 58513 |
rs78639980 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378671 | AGCGCCGCCACCTGG[A/G]GGGATGCTTGTCCCT | 58513 |
rs78663649 | snp | C/T | 0.10237 | 0.201756 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378636 | CCTGCTGCCTCCAGG[C/T]CTGTGATGAGCAGAT | 58513 |
rs78714622 | in-del | -/G | 0.114738 | 0.210248 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462322 | GGTACCACCAGGGCT[-/G]GGGTCCCGTTGCCAC | 58513 |
rs78725011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446785 | CGTGCTGGAGCATTT[C/T]ATTAAACAGAAGAGG | 58513 |
rs78735063 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442478 | AATATAGTCACTCAG[C/G]AAACAGCAGCAGCAG | 58513 |
rs78741581 | snp | C/G | 0.0770498 | 0.180522 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415438 | CCTCCTGCCCAGGGA[C/G]CCAGGACTTGTGCAA | 58513 |
rs78768325 | snp | A/G | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365775 | ACTGGCCTCTGGCAC[A/G]GCTGAGGGTCAGCTC | 58513 |
rs78784897 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466536 | TCACTGTTCCATCCA[C/T]TGCCCAGAAAGTGTC | 58513 |
rs78860807 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470230 | CCACTAAAAAAAAAA[A/T]ACAAAAATTAGCCGG | 58513 |
rs78907900 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365273 | CCCAACAATTGTTCA[C/T]ACGTTCAAGTCCTAA | 58513 |
rs78918233 | snp | A/G | 0.110519 | 0.207473 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403020 | GCGGTCCATGCTTGC[A/G]ATCAACTGTGGCCTA | 58513 |
rs78921522 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465058 | CACTCCAGCCTGGGC[-/A]ACAGAGCGAGACTTR | 58513 |
rs78944952 | snp | A/C | 0.031825 | 0.122064 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372002 | TGCCCAAAACAGACA[A/C]CTGCTGGTTATTTAA | 58513 |
rs79083128 | snp | C/G | 0.104859 | 0.203554 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445411 | TGACAGTGGTCAGAG[C/G]TTTTGATCTAATTAC | 58513 |
rs79086196 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406369 | AGTGAGTGTGCCAGG[A/G]AGGGAAGATGCTGGA | 58513 |
rs79112293 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, missense, synonymous-codon | EPS15L1 | GRCh38.p7 | 19:16356943 | TTAATGTCTCTCTGC[A/G]ATGCACTGCCTCTGA | 58513 |
rs79141594 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456816 | GCTTGGGGCCAGGTG[C/T]GCACCGGGACAGAGA | 58513 |
rs79157206 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379029 | GTGTTCCTGGCCGGG[C/T]GCACTGGCTCACGCC | 58513 |
rs79239382 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461515 | TGGTCCCAGCTACTC[A/G]GAGGGCTGAGGCTGG | 58513 |
rs79267697 | snp | G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468364 | AAGCTGACTTTTTTT[G/T]AGACTGAGTCTCACC | 58513 |
rs79355246 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367602 | TCTCGAGGCTGCGCA[C/T]GCCCCTAGCACCCGG | 58513 |
rs79376325 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470388 | CAATACTCCATCTCA[A/C]AAAAAAAAAAATTGG | 58513 |
rs79385967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360732 | CAGGCTGGGCAACAC[A/G]GCGAGACCCTGTCAC | 58513 |
rs79426952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362245 | AGAGCAGCTAAAACT[C/T]GAGTTGTCCTAGAAT | 58513 |
rs79528580 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439941 | TTTTTTTTTTTTTTT[C/T]TCAGATGGGGTTTTC | 58513 |
rs79575287 | snp | C/G | 0.0166325 | 0.0896639 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472185 | CCGTGCTCTCTTGCC[C/G]GTTCCCCTACTCCTC | 58513 |
rs79576962 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404187 | GGGCATGACCAAGCA[C/T]GAACAATCTGTCCAT | 58513 |
rs79578464 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363630 | AGTGCCTCCTCCCAG[C/T]TGGCCTCCGTTTCCT | 58513 |
rs79602214 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437474 | TTAGTGGTTGCCAGC[A/G]ACTGGGAGGGGGAGA | 58513 |
rs79609186 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367089 | GAGAGCTTTACTGAC[A/G]CGCATTTCAGAAAAG | 58513 |
rs79639770 | snp | A/T | 0.5 | 0 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354881 | CTCAGACCCTGTTTC[A/T]AAAAAAAATTTTTTT | 58513 |
rs79641498 | snp | A/C | 0.104859 | 0.203554 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410332 | GTGCTCCACACCCAC[A/C]ACGACGGCTAGAAGG | 58513 |
rs79670178 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466427 | CATCTCACAGCATCA[A/G]TCCCCACCGAATGCA | 58513 |
rs79707488 | snp | C/T | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384624 | TCTGGTAACCAGCCT[C/T]GCTGCTGTCCTCCTT | 58513 |
rs79788231 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459032 | ACAAACCTGGGCAGC[A/G]TGGCCCGGTACAGAA | 58513 |
rs79788478 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405335 | GCACCCCACAGGCCA[C/T]GCCAAGGAGACTGCG | 58513 |
rs79855306 | snp | A/C | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441484 | CAAAAAAAAAATTAG[A/C]CGGGTGTGGTAGCAT | 58513 |
rs79878641 | snp | G/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467163 | TTCTTTTTTTTTTTT[G/T]TGAGACGTAGTGTCA | 58513 |
rs79897354 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448187 | TGACACCAAAAGCCC[A/G]ATTCACAAAAGGAAA | 58513 |
rs79907489 | snp | G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424677 | AATACTTTTTTTTTT[G/T]GAGATAGAGTTTCGC | 58513 |
rs80027128 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461771 | TAGCAGGGCCCCAGC[A/C]CTGGTGGTGCCCTGA | 58513 |
rs80029734 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437980 | TTCAACAATGAAGGC[A/C]GTCCGTGCAAAAACC | 58513 |
rs80058032 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356510 | AGAGACGGGGTTTCA[C/G]CATGTTGGTCAGGCT | 58513 |
rs80085530 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361597 | AAAACAGTTTCTCAA[A/T]AAAAAAAAAAAGAGC | 58513 |
rs80180964 | in-del | -/G | 0.24449 | 0.249939 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435657 | CTGCAGGTCTTTCTC[-/G]GGGGCCTGGGATCCT | 58513 |
rs80222503 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463965 | TGCGCAGATGACAGA[A/G]AGAGGGGCCAGGGGG | 58513 |
rs111234097 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473934 | ACTGCACTCCAGTTT[A/G]GGCAACAAGAGCGAA | 58513 |
rs111241134 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400359 | AAAAAACAAAAACAA[A/C]AAAAAAAAAAAACCC | 58513 |
rs111241325 | snp | C/G | 0.5 | 0 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421419 | CCAGGTCGGTCTTCA[C/G]GAATATCTCATCAAA | 58513 |
rs111245127 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412817 | GCGGCCGTGGACAGC[A/G]CCGGAGCCGGGACCA | 58513 |
rs111429751 | in-del | -/AT | 0.389715 | 0.207315 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412633 | TCTCTATTTGGAAAA[-/AT]ATATATATATATATT | 58513 |
rs111468468 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449221 | CAAGACCAGCCTGGG[C/T]AACATAACAAGATCT | 58513 |
rs111555379 | snp | A/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367988 | GAGAGAGAGAGAGTG[A/T]GTGTGTGTGTGTGTG | 58513 |
rs111556949 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424897 | TGATCTCCTAACCTT[A/G]AGATCTGCCCACCTC | 58513 |
rs111558240 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393571 | GGAGAATGGCGTGAA[A/C]CCGGGAGGCGGAGCT | 58513 |
rs111593959 | in-del | -/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434936 | GTACAGGAAGTCCTC[-/T]TTTTTTTTTTTTTTT | 58513 |
rs111751366 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394993 | GTGGGGCTGAGGCGG[A/G]TGGATTACCTGAGGT | 58513 |
rs111818623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420663 | AGCAATTCTTTCCTT[G/T]TGATAGCTCCCAAGT | 58513 |
rs111855428 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471721 | GTGCCCGCGAGGGTC[A/G]CTCGGGCACGGGAGG | 58513 |
rs111863051 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471216 | TCTGGAAGAATGCAG[C/T]GCTCCCAGCACCTGA | 58513 |
rs111870777 | snp | G/T | 0.5 | 0 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355234 | TTTACAGAGATTAAA[G/T]AAGCTTCTCTTGTTT | 58513 |
rs111917473 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392129 | GCCAGTGAGCTCCCT[C/T]ACTCAGCAGGAATGA | 58513 |
rs111923053 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432215 | GAGGCAGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 58513 |
rs111974305 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453052 | TGATCTGCCCGCCTC[A/G]GTCTCCCAAAGTGCT | 58513 |
rs111980636 | snp | A/G | 8.28988e-05 | 0.00643759 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404561 | GCCTGTGCATAGGGC[A/G]CTGCCCCGGAGGTGG | 58513 |
rs112002860 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403624 | CCTCCCAAAAGAGAC[C/T]CTCACGTAAGTAACA | 58513 |
rs112068280 | snp | C/T | 3.29924e-05 | 0.00406142 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392278 | CAGGCACGCAGCTCT[C/T]CCGGGCAACGTCCCA | 58513 |
rs112120269 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407973 | TCTAAGAAGTTTGGG[A/G]GTGATAACACAGAAT | 58513 |
rs112124861 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378509 | CAGAGCTCTCCCAGG[C/G]CTCTCCCTGGGGCTG | 58513 |
rs112126069 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372327 | ATGCCAGCCACACCA[A/C]ATGTCAATTTCACCT | 58513 |
rs112164729 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467935 | AAAAGGGGAATAAAA[A/G]CCTCCTAGAATGGAG | 58513 |
rs112260974 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470213 | ATGGTGAAACCCCGT[C/T]TCCACTAAAAAAAAA | 58513 |
rs112350245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463975 | ACAGAAAGAGGGGCC[A/G]GGGGGCCACAGAGCA | 58513 |
rs112389286 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364106 | TCAGGGTTGGAGGGC[A/G]AGCTGTCCTGGGCTC | 58513 |
rs112490789 | in-del | -/A | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371763 | CACTTAAAAAAAAAA[-/A]TCTGTTTCTCTCTTT | 58513 |
rs112508806 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462375 | CAGAATCAGGGAAGT[C/G]GGGGGGAGGGCATGG | 58513 |
rs112613043 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464995 | GAGGCAGTAGAATGG[C/T]ATGAACCCAGGAGGC | 58513 |
rs112621899 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371985 | AAGAAACCAGTTTCT[C/T]CTGCCCAAAACAGAC | 58513 |
rs112643671 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426677 | AAAACAAAAAGTCCA[C/T]GTCAAGAGACACGAA | 58513 |
rs112651764 | snp | C/G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405236 | AGGGACAGAGCCTGG[C/G/T]GGAGGGAACCACAGG | 58513 |
rs112710114 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428515 | GGAGAGAGAGAGAGA[A/G]AGAAAGTGAAAGAAA | 58513 |
rs112767263 | in-del | -/TGAGAT | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395934 | GGGCGATAGAGTGAG[-/TGAGAT]TCTATCTCAAAAAAA | 58513 |
rs112839244 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400372 | AAAAAAAAAAAAAAA[A/C]CCCTGACTTTTGAGA | 58513 |
rs112919093 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429709 | GGGGCCCTGTCACCT[A/G]GCTGCTGCTGAGCCC | 58513 |
rs113013807 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404848 | TCCAGGGGAAGCCTC[C/T]GAAACCACCCACTGT | 58513 |
rs113029344 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418997 | TGTGCCCAAATGAGG[C/T]TGCCACAGGGGCATG | 58513 |
rs113045527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459145 | GCAGTATAATCTTAC[A/G]GGAGCACTGTCACAT | 58513 |
rs113088848 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378568 | ACTGAGCCACAGAGA[C/T]ACGCTTCCAGGCCTC | 58513 |
rs113090367 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431153 | CTGAGACAGGAGAAT[C/T]GCTCGAACCAGGGAG | 58513 |
rs113116134 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427981 | GGCCAAGGCGGGTGG[A/T]TCACTAGGCAGGAGA | 58513 |
rs113127480 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471730 | AGGGTCGCTCGGGCA[C/G]GGGAGGCCGCGGGTC | 58513 |
rs113133943 | snp | A/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395938 | CGATAGAGTGAGTCT[A/C]TCTCAAAAAAAAAAA | 58513 |
rs113141024 | snp | A/C | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426353 | AAATGTCCACGTTGA[A/C]ACCAGGCATGGTGGC | 58513 |
rs113149695 | snp | G/T | 0.112631 | 0.208878 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422932 | CACTGCACTCCAGCC[G/T]GGGCGACAGAGCAAG | 58513 |
rs113163724 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428278 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 58513 |
rs113212693 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449939 | CATCACATAACATCA[G/T]TAAAATGATAAAATT | 58513 |
rs113234041 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391834 | GCACTTACTCCTGCC[A/G]TGACGGGAGCACCTA | 58513 |
rs113305300 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384873 | ACTTCACCGTCTGAG[A/G]CCTGATGGTCGTCAG | 58513 |
rs113310652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362147 | GGGGAATCCCAGTTT[C/T]AATCAGCTTTATCCC | 58513 |
rs113324840 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465974 | GTAACAATCTCTGGC[C/T]TCACTTTATCTATTT | 58513 |
rs113341124 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464951 | AGGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 58513 |
rs113363719 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381930 | ATGTGCTGGCTTCTG[A/G]GCCACATCTCCAGAC | 58513 |
rs113400958 | snp | C/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404520 | CCCAGGTAACACGAG[C/T]TCAGGGGAGTCCTTG | 58513 |
rs113466625 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374651 | GGTTTAGGTACGTGG[A/G]GAGGCGGGGGTGGCG | 58513 |
rs113505233 | snp | G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369695 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTAG | 58513 |
rs113506345 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381407 | CAGGGCCTCGTCCTG[G/T]GCAGACTGTCCTGCC | 58513 |
rs113520026 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438019 | CGTTGGGCTGAACTG[A/G]ACTCACCTTGGGGAC | 58513 |
rs113591080 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421492 | CTGAAACAGTTTTTG[A/G]CAAAACAGTTAATCT | 58513 |
rs113607870 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434268 | CAGGGAGAAAACAGA[A/G]CAAGAGCCTTGTAAG | 58513 |
rs113627332 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443624 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 58513 |
rs113683256 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431476 | GCCCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 58513 |
rs113712937 | snp | A/C | 0.444444 | 0.157135 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400356 | AAAAAAAAACAAAAA[A/C]AAAAAAAAAAAAAAA | 58513 |
rs113745605 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369113 | CAACGTCTTCCTCTG[A/G]CTCCCATCTAAGACA | 58513 |
rs113775789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434146 | GAAGTGGAAGGATTC[C/T]GGCACCTTCCCCAGG | 58513 |
rs113777061 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378110 | GGACGAATGAATGGC[A/G]GGTGGGTGGATGGAT | 58513 |
rs113777372 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428445 | AGGAAGGAAGGAAGG[A/G]GGGAGGGAGGGAGAC | 58513 |
rs113779505 | snp | A/G | 0.106987 | 0.205054 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417171 | TGGGACAACACAGCT[A/G]CCACAGGCTGTGCCC | 58513 |
rs113826134 | snp | A/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436141 | AGATACCCCCACCCA[A/G]CCCATGACCTCTCCA | 58513 |
rs113915959 | in-del | -/G | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391938 | GCATGTGGTGCTTGT[-/G]TGATTTAGTCTTTTT | 58513 |
rs113971841 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412415 | TGAGACAGGGGAATC[A/G]CTTGAACCCAGGAGG | 58513 |
rs113986365 | snp | G/T | 0.5 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370713 | CTGCCTGCAGTCAGT[G/T]TAAACATACAAGGCT | 58513 |
rs114096533 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411899 | AAACAGGGTCCCACT[A/G]TGTTGCCCAGGCTGG | 58513 |
rs114142682 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442965 | CAGACACTTCCCGCT[A/G]TGTCCTGAGCTCTGC | 58513 |
rs114148592 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404518 | TTCCCAGGTAACACG[A/G]GCTCAGGGGAGTCCT | 58513 |
rs114152425 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370697 | TGCTCCAAACGGCAA[G/T]CTGCCTGCAGTCAGT | 58513 |
rs114256252 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405889 | GCTGAAATAGCACAA[C/T]GGGCATTGTGACAAG | 58513 |
rs114264188 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397732 | CAAACAGGTTCATTT[A/C]AACGAGAAGAAAAAA | 58513 |
rs114267688 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363504 | CTTTCCCTCTGTTCC[C/T]CCAGCAGATCAGCCA | 58513 |
rs114328661 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473371 | AAATTAACCCAGTGC[A/G]GTGGCAGGTGCCTGT | 58513 |
rs114370264 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433514 | CCTTGAGCTTTATCA[A/G]AAGAAAAAGAGTAAT | 58513 |
rs114375125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365891 | AGTGGGCTTCAGGAG[A/G]TCCTGGTGAACCAGG | 58513 |
rs114414261 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426404 | CTTTGGAGGCCGAGA[C/T]GGGCAGATCACCTGA | 58513 |
rs114473313 | snp | C/G | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393153 | AAATCCATAGAGACA[C/G]AAAATAGGTTGGTGG | 58513 |
rs114624587 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466485 | CTGGGCCCCTCCCAA[C/T]GATGTCAGCCCCGTG | 58513 |
rs114626355 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436336 | ACCATGCTCACTTCC[C/T]TTAGAAGGAATTCTG | 58513 |
rs114632011 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404147 | TCCCACTGTGGCTAA[C/T]GGAAGATCACTTTGG | 58513 |
rs114682907 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444700 | AATGATCAGAGAGGT[C/G]TGGATCTGAAGCACA | 58513 |
rs114686657 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411502 | CAGGTTCTAACTCGA[C/T]AGAGTGATGGTTAAT | 58513 |
rs114767904 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459175 | TATGCAGTCCATCAT[A/G]GTTATGCGGTGCGTG | 58513 |
rs114875025 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458134 | TTCCTGACAGTGGGG[G/T]GTGGCTCCCTGCCAA | 58513 |
rs114905557 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435730 | CAGAAATGTTCACAA[C/T]GGAAACAAACACTTG | 58513 |
rs114925949 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402604 | TGGAATGTAGTGGAG[C/T]GATCATAGCTCACTG | 58513 |
rs114931124 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399975 | CTCTCCATAAGTTGA[C/T]TGGATGGTGAGCAAG | 58513 |
rs114971579 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434002 | ATAAATAAATAGACA[C/G]AGACACACATTCCCA | 58513 |
rs114986409 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437156 | ACCCAGCAATTCCAC[A/T]CCTACGTATTGACCC | 58513 |
rs115077875 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450795 | GCCAGGGCATGTCCA[A/G]CTTCTGCTGGTCTCG | 58513 |
rs115079403 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419773 | TTATCCCCACAGTTC[A/C/G]AGGCCCTGACGATTT | 58513 |
rs115088110 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410609 | ATGAGGGATGGATGA[A/G]TAAAATGTGGCCCAT | 58513 |
rs115140590 | snp | C/T | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364325 | AGTGCCCAGCCCACG[C/T]GGGCAGGACAGGAAT | 58513 |
rs115165567 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380315 | CACCTAAGGCTCTGG[C/T]GTCTAATCACACAGA | 58513 |
rs115197240 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381345 | CTCCCAGGCTGGGGC[C/T]ACCAGACGCTGCCCT | 58513 |
rs115261368 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382002 | CTACCCTCTGTGTCG[C/T]GCAATAGGACCCGGG | 58513 |
rs115277133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405818 | GGCAGAGGCTTCTCA[C/T]CTCCTGATTTTCAAC | 58513 |
rs115358821 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375382 | CGTGTACGTGCACAT[A/G]CATGCATAAAAATAC | 58513 |
rs115492068 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380967 | TCGGCCCAGTCAGAG[A/C]CACATCAGAGACAGA | 58513 |
rs115558616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441132 | ATCCAGGTGCACTCA[A/G]CTCCCAAGCCAATGG | 58513 |
rs115562850 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384749 | CGACTCTGAACACTC[A/G]CTGGCCCACTTTCCC | 58513 |
rs115602846 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363199 | CCAACGGAGTCCCTG[A/G]GCATTCAACGTGGTC | 58513 |
rs115643709 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428905 | TCAGGACCAGTCCGC[A/G]AGTTCTCAGAAAAAC | 58513 |
rs115804462 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440576 | TCCACGAGAGACTGG[C/T]CCAAAATAAAAAGTC | 58513 |
rs115813954 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357168 | TCTCCACCACACGCA[C/G]CACTAGGTCTGCGTG | 58513 |
rs115877595 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456991 | GGCCAGCAAGGTGGG[C/T]GCATATGCATATGAG | 58513 |
rs115887586 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414345 | GAGCCCAGCCCAGCC[A/G]ACGCCTTGACCTCAG | 58513 |
rs115905707 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428843 | CGGAACTCAGACTCT[C/T]AGCCGTGGCACTCAC | 58513 |
rs115909891 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446384 | TCTGCTAGCAAAGTA[C/T]GCGCTCTTGTGCAAA | 58513 |
rs115911123 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415944 | CACATCCTTGCTGAT[C/T]GCCAGTTTGGATAAC | 58513 |
rs115970798 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436245 | TTCATGTCAGGATTT[A/G]AGCCACATAAACGTG | 58513 |
rs115984017 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369431 | GAGCCACTGCTGGCC[A/G]CTGTGTTTTCCTGCC | 58513 |
rs116050387 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427194 | CTGTCGGAGGCCAAG[C/G]GGGGAGGTCGCTTGA | 58513 |
rs116051765 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473544 | AATGAATACATAAAC[A/G]ACTACAGGGGACTGA | 58513 |
rs116054133 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441198 | GCAAGTGGCCAAGCG[C/T]GGTGGTTCACGCCTG | 58513 |
rs116122335 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465578 | GTCTCAGTTCCTTGA[G/T]AGGCTGAGGTGGGAG | 58513 |
rs116140880 | snp | C/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409986 | TAAAAAGAACCCAAT[C/T]AACCAGGTGTAGTGG | 58513 |
rs116161742 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420056 | AAAGCCTCTGTCTTC[A/G]TGCTCCCCCTCCTCC | 58513 |
rs116246556 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424418 | AGAGGTGGGTTATGA[C/T]GCTGGGTGACCTGTG | 58513 |
rs116247923 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414679 | ACTGGAATTATAGGC[G/T]TGAGCCAACACGCCT | 58513 |
rs116263856 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400875 | TTTATCCAAGAAAAC[C/T]GGTTTCTAAAAACCT | 58513 |
rs116284145 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463027 | CCCAGCTGCAGTTGA[A/G]CTGACCTGGAGGGTG | 58513 |
rs116296355 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441109 | GTCAGCGGCAGGGCC[C/T]AGAGGACATCCAGGT | 58513 |
rs116367835 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465615 | TTGAGGCCAAGAGTC[A/G]AGGCTGCAATGAGCT | 58513 |
rs116405553 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380074 | CTAGTCACACAGATG[C/T]GGCTGCCAAAGGCTC | 58513 |
rs116420336 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371285 | CTGCATCCTGTGTGG[C/T]ACCCCCGGCAGGGAG | 58513 |
rs116432921 | snp | A/C | 0.031825 | 0.122064 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368766 | AAACCATCATTCACC[A/C]TACACAACACAGACA | 58513 |
rs116453289 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412973 | CAAGGAATCTGAGAT[A/C]ATTGACTTTTGCCTG | 58513 |
rs116487268 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403093 | TAAAAGAAGTGTGCC[G/T]GGCCACTCCGACACA | 58513 |
rs116488216 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446024 | TGCTAAGAGACAACA[C/T]GCAAAGTTCCTGTGG | 58513 |
rs116696550 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381401 | TGGGTCCAGGGCCTC[A/G]TCCTGGGCAGACTGT | 58513 |
rs116717777 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438059 | ATGAATACACTAAAA[G/T]GGACTTATCCTGGCC | 58513 |
rs116799462 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459174 | ATATGCAGTCCATCA[C/T]GGTTATGCGGTGCGT | 58513 |
rs116858660 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410268 | GGAAAGATACTTGAC[A/G]TCGCTAGGGAAGCAT | 58513 |
rs116860620 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375773 | GTCATACTTTTTCTC[C/T]TGACTCATCCACAAG | 58513 |
rs116873381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439353 | GAGGAACTGCATTAA[A/G]CAAAGTCAAATTTAT | 58513 |
rs116875885 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429402 | GGCCAACGCTGGGCA[C/G]GCTGCCAGTCCCCGG | 58513 |
rs116882126 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444874 | TGGGACTACAGGTGC[A/G]TGCCACCATGCCCAC | 58513 |
rs116923291 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470836 | ACAGTAATTATAGGA[A/T]CACTGAGTGCCTCTC | 58513 |
rs116964769 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430897 | ACAGATGAATGGATC[A/G]TAGGGATGCGGAGGG | 58513 |
rs117047710 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406555 | ACCCTGGCCCCATCA[A/C]CGGGTAACGCTGGCA | 58513 |
rs117061321 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445629 | AGCCCCAGGCAGTCT[G/T]TCACTGGCCCCTGTG | 58513 |
rs117154809 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400088 | ACGCCTGTAATCCCA[A/G]CATTTGGGGAGGTCG | 58513 |
rs117157819 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397871 | GTTAATAAAGACACA[A/C]CCTCAGTGAAAACAT | 58513 |
rs117195970 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422550 | TGTGGCTGGAGGGAT[C/T]GATTGTTCCTTCTCC | 58513 |
rs117196542 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467446 | TCAGCCACTGCACCC[A/G]GCCTGGAAAGTTGTT | 58513 |
rs117243981 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375739 | AAAATCTGCTCTAAA[C/T]CCACACAGCCCATAC | 58513 |
rs117294274 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450276 | TTCAAACCTTGATTC[C/T]GTGCTCTGATGCCCT | 58513 |
rs117314160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391371 | ACTACAGGTCTTAAG[A/G]ACATTAAAAAGGGGC | 58513 |
rs117385850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407588 | GACTCAGTCTCCCAA[A/G]GTGCTGGGATTATAG | 58513 |
rs117412491 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368866 | CAACACAGATGCCCA[C/T]ACAACTGCCAGGTTT | 58513 |
rs117492537 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375597 | CTGTGTAAGGCACAG[A/G]TGGCCTCTTGCAGAT | 58513 |
rs117520868 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469833 | CTGCAGGGTGCTTCC[A/C]TTTTGCCCCCAACCA | 58513 |
rs117563475 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445286 | CGGCTCGAACACTTG[A/C]TGACCACCGGATGTC | 58513 |
rs117579615 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406513 | GCTCCCACCAGGGAC[A/G]GAAGCCTCTAGAGCC | 58513 |
rs117601515 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367835 | GCAAACCATAAAAAC[A/G]GTGAATGCTATAAAA | 58513 |
rs117799475 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461416 | GCTTTGAGCTCAGGA[C/G]TTCGAAACTGGCCTA | 58513 |
rs117863322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373430 | TTGGTTTGTTTGTTT[C/G]TTTTAAGAAAACATA | 58513 |
rs117865880 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388014 | CAGAAAAAACAAATT[A/T]GGAGAACTGACAGCT | 58513 |
rs117866384 | snp | A/C | 0.0314385 | 0.121371 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472131 | GCGGGGCCGCCCACA[A/C]GCAGCCTGGAGGGGC | 58513 |
rs117934862 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428903 | TTTCAGGACCAGTCC[A/G]CGAGTTCTCAGAAAA | 58513 |
rs117956865 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460698 | CAGCACGGGGGTGCC[A/G]CGGGCACAGAGCGTT | 58513 |
rs118028279 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359716 | AACATTTTAAAATTA[C/G]CCAGATGTGGTGGTG | 58513 |
rs118044657 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405946 | GCGTGGTGCAAGGGG[C/T]CATCAGGACGCAGGA | 58513 |
rs118102021 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408263 | AACCCCAACAGTCCA[C/T]GGAGTCCACACAATC | 58513 |
rs118134296 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405122 | CCAAGGGGGTCACAG[A/G]GAAACTACAGTCACA | 58513 |
rs137871930 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423183 | AAACAAGGGATACCA[C/T]GTGACCCAGATCAGC | 58513 |
rs137884743 | snp | C/T | 3.37012e-05 | 0.00410481 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402478 | AGCTGGGAAAGTTTG[C/T]TCCTTGCCTGTGCAA | 58513 |
rs137900854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464569 | CCCCAAAGTCCCAGC[C/T]GCATGTTTTGGCCCT | 58513 |
rs137911389 | snp | A/G | 0.00060594 | 0.0173955 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361836 | TTTAGCTGCAGAGGA[A/G]GGGACAAATGGGTCT | 58513 |
rs137966691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431276 | AAATAAATAAATAAT[A/G]CTTATATTTATGGTT | 58513 |
rs138026273 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418047 | CTGAATGAAATACAT[A/G]GCTAACGCGAATTGG | 58513 |
rs138044111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413905 | GCCTCCACCCCTTCC[C/T]AAGGCCTGATTCTGT | 58513 |
rs138049908 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386005 | AAGGGGAGCAGCAGC[A/G]GGTGCTTGTTTTGGC | 58513 |
rs138054959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358913 | TAGAAATGCCACTTC[C/T]TAATACACACATTTG | 58513 |
rs138112264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444600 | TGACAGTGGTCAGGT[C/T]TAGGCAGCAAACAGC | 58513 |
rs138158709 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444051 | CCCAGGCGACGGTGC[A/G]AGACTCCGTCTCAAA | 58513 |
rs138161259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382053 | TGGACGTCCAAAGTT[C/G]TAAGACCTGGTGACA | 58513 |
rs138161750 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374599 | ACACGATGGGAGGTG[A/G]TAACTGAGGGAAAGT | 58513 |
rs138162235 | in-del | -/TC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439071 | TTAGCTTGTTTTTTT[-/TC]TGTTTTTTTTTTTTT | 58513 |
rs138191605 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403332 | GCCTCCTGAACACAC[C/G]AGTGGCTGTGGAGGA | 58513 |
rs138212301 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473815 | AATACAAAAATTAGC[C/T]GGTTGTGGTGGTGGG | 58513 |
rs138243594 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384775 | TTCCCTGGACGCCTC[A/G]CACCTGCAGGCCTGC | 58513 |
rs138356793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413649 | TTCATTCTGCAGCCC[C/T]CAAGAGCTCATGTTT | 58513 |
rs138370661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430771 | CACGGATGCAAGTGC[A/G]CACGGATGAATGTAT | 58513 |
rs138475789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467281 | AGGGTCCCGAGTGGC[C/T]GGGATTACAGGCGTC | 58513 |
rs138497536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363433 | TGCCTTCCTCATCCG[A/G]TAGAACGAGCCCACA | 58513 |
rs138498967 | snp | C/G/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464881 | AAGGTCAGATCGAGA[C/G/T]CATCCTGCCTAACCA | 58513 |
rs138527137 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456185 | AGCCTGGGCAACAAG[A/G]GGAAAACCCTGTCTC | 58513 |
rs138599343 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379414 | TCTTTAACTTTCTCC[A/C]CAGCAGGGAAGGCCT | 58513 |
rs138619389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358662 | TAGACAGCTCGGCAC[A/G]CTGGGCGATGGGATG | 58513 |
rs138655258 | in-del | -/C | 0.115438 | 0.210697 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461544 | GGAAAATCACTTGAA[-/C]CCAAGAGGCAAAGGT | 58513 |
rs138663632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398409 | ACAGTGCTGAGTGGA[C/T]GTCAGGTGCTGACGA | 58513 |
rs138672096 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390835 | TTCAAATATATGAAA[C/T]ACATGTAAAGCAGTG | 58513 |
rs138692695 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422800 | CCTCTCTACTAAAAA[C/T]ACGAAAAATTAGCCA | 58513 |
rs138696530 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464855 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACAAGGT | 58513 |
rs138706027 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368920 | AGCAGTGGCCCGGGC[A/G]GGGCACCACTCCAGC | 58513 |
rs138732804 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408111 | AGCTCTGGACACCAG[C/G]TAACAACAGTGTGGA | 58513 |
rs138734142 | snp | A/C/G/T | 0.000115526 | 0.00759947 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417990 | CGGGACCATGTCCGG[A/C/G/T]GAGAGGACTTGAGGA | 58513 |
rs138736176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459801 | GGGAGGGAGGTCAGG[C/T]AAGGCTGTGAATCAG | 58513 |
rs138765079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396375 | CAAGTGATCCTCCCA[C/T]GTCGGTCTCCCGAGT | 58513 |
rs138810242 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438889 | TCATATCTGTGGTTC[A/C]CCACGATCCCCTCGG | 58513 |
rs138863131 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448824 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 58513 |
rs138881627 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434682 | CCTGAAGGAAATAAC[A/G]TTATGGCAACCTCGG | 58513 |
rs138975721 | snp | C/T | 6.59718e-05 | 0.00574296 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402380 | TCAGGTTGGCCAGGT[C/T]GGTCAGGCTGGCACC | 58513 |
rs138995350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399568 | TCAGTTCTCTCAGAA[A/T]AAAGCCCTGGTTTAG | 58513 |
rs139037371 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381032 | CATTCCAGGTCCCCC[A/C]GATAAGGGCAGTGGC | 58513 |
rs139054167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446316 | TGGCCGAGGGCAGGA[C/T]GCCTCCTACATCTTC | 58513 |
rs139059833 | snp | C/T | 0.281049 | 0.248064 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451557 | TTTTTGAGATGGAGT[C/T]TTGCTCTGTCGCCCA | 58513 |
rs139068497 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457168 | CCAGTTCCCTAAAAA[C/T]GAATGTGTTTCCTTG | 58513 |
rs139070904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379766 | TAAGGCTACAGTGTC[C/G]AGTCACACCAGTGCA | 58513 |
rs139072328 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388464 | ACTGAAAACCAAAGA[C/T]AAAGAGAGAATCTTG | 58513 |
rs139100130 | snp | G/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448568 | GGGGAGAAAGGCCGG[G/T]CGCGGTGGCTCACAC | 58513 |
rs139109227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419713 | CCGTGAACAGAGCTG[C/T]GGAGAATGAGCAGAT | 58513 |
rs139109371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376251 | GGAGGCGTCCCAGAC[C/T]GGGGCACAGATGGAA | 58513 |
rs139185816 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379026 | CATGTGTTCCTGGCC[A/G]GGCGCACTGGCTCAC | 58513 |
rs139231916 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460914 | ATCATCAAGTTTTTT[C/T]GTGTTTCATCTTTCC | 58513 |
rs139234501 | snp | C/T | 9.88663e-05 | 0.00703018 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404637 | TCGCTCAGCATGTCT[C/T]GGAGCTTGGCCTTCT | 58513 |
rs139252408 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432020 | TATGTGCAGGACTGA[C/T]TGCAGGACTTGAGTA | 58513 |
rs139335823 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465655 | CCACTGTACTCCAGC[A/G]TAGGCAATAGAGCAA | 58513 |
rs139341545 | snp | C/T | 4.95152e-05 | 0.00497545 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436976 | AGAGGGCGGTGTGAC[C/T]ATCAGAGGGCTGCTG | 58513 |
rs139388695 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393023 | CTCCAGCCTAGGCAA[G/T]AGAGTAAAACCCCAT | 58513 |
rs139482344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410433 | TGTAAAATGGTACAG[C/T]CACTTTGAAAAACAG | 58513 |
rs139490747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359598 | GGGCACAGGGGCTCA[C/T]GCCTGTAATCCCAAC | 58513 |
rs139491464 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423930 | AGAGTCCTAATAATA[A/C]TTGCTGGGCAAACAA | 58513 |
rs139533895 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356235 | GCAGACAATTCTGCA[C/T]TCTGGGAATGTGGTA | 58513 |
rs139554016 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469951 | GCCATGCCTCACACC[C/T]GGGCCAACAGTAACC | 58513 |
rs139556976 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366090 | ATGGATCAAATAGCA[A/T]GATTCTAGCAGAGGA | 58513 |
rs139563148 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435618 | CGCATGCTTTCACAG[C/T]TGTTGGTGCTAAGAA | 58513 |
rs139574804 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397420 | CTGAAAGTTAAACAA[C/T]TTTTTTTTAATCAAT | 58513 |
rs139576017 | in-del | -/ACTAAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464762 | ACACTAACACTAACA[-/ACTAAC]CTAACACTAATGATA | 58513 |
rs139593111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465216 | CTACACCAAACACGC[C/T]CTCTCCTCCATACAA | 58513 |
rs139643677 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374815 | GTAAATGTGTGTACA[C/T]GTATGTAAGCACAGA | 58513 |
rs139684048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370000 | TGCCAATGTCGCAGA[C/T]GCCACCTCTGCAAAG | 58513 |
rs139694029 | snp | A/C | 0.00125427 | 0.0250112 | synonymous-codon, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377150 | AGGCCGTGGAGGAGC[A/C]GGTTTCTTCGGAGGC | 58513 |
rs139702035 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440980 | AACAAAAACCAGAGC[C/T]GCCACCACCCCATCA | 58513 |
rs139731103 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360095 | TGCTTTTCGAAAAAA[C/T]GAGCCCTTTGCGGGT | 58513 |
rs139740187 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436224 | TATTTGAGAGCAAGA[C/G]TGTTATTCATGTCAG | 58513 |
rs139784678 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470153 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTCGAG | 58513 |
rs139821283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382340 | TCCTACTCGGGCAGC[A/G]GCTTCAAGGAAAATC | 58513 |
rs139831954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452616 | TCCGGCCTGCACAAC[A/G]TAGCAAAATGTCATC | 58513 |
rs139849142 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450612 | CAGCCTCCCAAGTAG[A/C]TGGGATTACAGATGC | 58513 |
rs139911009 | snp | A/G | 0.000751233 | 0.0193663 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361914 | GCCGCTGTCAGCCCC[A/G]AGTGGCTGGAATGGA | 58513 |
rs139944694 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355970 | GCCCAGCGGAGGGTC[C/T]GATGTGCAGGGGATA | 58513 |
rs139958771 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453586 | AGCGTGGTGGCAGGC[G/T]CCTGCAGTCCCAGCT | 58513 |
rs140041191 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435194 | TGGCCTCAAGTGATC[C/T]GCCTGCCTCGGCCTC | 58513 |
rs140046934 | in-del | -/C | 0.0991586 | 0.199366 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384169 | AGCAGGCCCCTGCAG[-/C]CCCCCGAAGACAGAG | 58513 |
rs140061318 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432472 | ACTTGGGAGGCTGAG[A/G]CAGGAGAACGGCGTG | 58513 |
rs140083029 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428133 | TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAAC | 58513 |
rs140122388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424221 | TGGCCTGGAGATGAG[A/G]AAGTTGGAGTAGGGG | 58513 |
rs140126191 | in-del | -/AAAC | 0.253001 | 0.249982 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449248 | ATCTGATTTCTTAAA[-/AAAC]AAACAAACAAACAAA | 58513 |
rs140159156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461819 | TGGGCTCGAGCAGGC[A/G]GCTCTGGGCCCTGTG | 58513 |
rs140189030 | snp | A/G | 0.000594796 | 0.017235 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402357 | CTCTGCCAGGGAGAC[A/G]CCTTCGCTCAGGTTG | 58513 |
rs140199949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458295 | AGGCTCCCGGACCCC[A/G]CAGTGAGCAGAAAGA | 58513 |
rs140207205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437985 | CAATGAAGGCCGTCC[A/G]TGCAAAAACCCCTTG | 58513 |
rs140220902 | in-del | -/AAATACAAATAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432588 | AATAAATAAATAAAT[-/AAATACAAATAC]AAATACAAATACAAA | 58513 |
rs140261711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371526 | GCGGCTTTGTTTAGG[A/G]GGTGAAAAGGTCATT | 58513 |
rs140287915 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441340 | AGCCGGGCGTGGTGG[C/T]AGGTGCCTGTAGCCC | 58513 |
rs140338228 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356637 | TTCTCCCAGAACACT[C/G]ACAAAAGGTGTGGCA | 58513 |
rs140355624 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426400 | AGCACTTTGGAGGCC[A/G]AGACGGGCAGATCAC | 58513 |
rs140369912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395594 | AGAATGATTTAGCCA[A/G]GAGTTCGAGGCTGGC | 58513 |
rs140396547 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433888 | GAATTGCTTGAACCG[G/T]GGAGGCAGAGGTTGC | 58513 |
rs140409155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459980 | CCCAACATCTAGGAT[A/G]GAACAATATTTCAGT | 58513 |
rs140462621 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384403 | TCCAGCAGTTTCTTC[C/T]GGAAGGCACCTCAGT | 58513 |
rs140482815 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425761 | AGTGAGCTGTGATCG[C/T]GCCACTGCACTCCAG | 58513 |
rs140503601 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408459 | TGAAACCCAGTAAAA[C/T]ACAAATTTGTAAAAA | 58513 |
rs140521600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406113 | CAGCCTGGGCTGCTG[A/G]GGTGGCTGGTGCCCT | 58513 |
rs140562399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445815 | GGATGAGGCCTGCAC[C/T]GTAAGAGGCTGCAGG | 58513 |
rs140566823 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450826 | CAAGGTGGTCATTTG[C/G]GTCCCCAGAGAATCC | 58513 |
rs140569601 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380524 | ACACACACGCAGCCA[C/T]CTAAGGCTCTAGCGT | 58513 |
rs140616676 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463465 | CCATATCACAGAGAC[C/T]GTCTCGGAGCTAGAA | 58513 |
rs140658070 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368391 | GGCTACACAACTGTC[A/G]TTCATCCTGCACAAT | 58513 |
rs140658199 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411197 | GGAAAACCCAAATAT[C/T]CCCCGATGGGAGGAA | 58513 |
rs140677537 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407424 | GATTCTCGTGCCTCA[A/G]TCTCCCGAGTAGCTG | 58513 |
rs140677972 | snp | A/C/G | 0.000151045 | 0.00868924 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417949 | CCAGCACCACTCACC[A/C/G]GGCCGGGCGTGCCTC | 58513 |
rs140701326 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424611 | AGCCAAGGAGTTCAA[A/G]ACCAGCCTGAGTAAC | 58513 |
rs140782885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402129 | GTTCTGGAAGCCAGG[A/T]TTCAGCATGGCCACC | 58513 |
rs140810818 | snp | A/C/T | 0.00016528 | 0.00908924 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441955 | AGCTTCACTCGCCCC[A/C/T]ACCCTCCCTGTGTAT | 58513 |
rs140857946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357919 | GAGAAAAACAAGGAA[A/G]AACCAACAAGTGCAG | 58513 |
rs140859526 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409963 | AAAAAAAAAAAAAAA[-/A]TCAGCTATAAAAAGA | 58513 |
rs140865748 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430538 | ATGTGTGTCTTCACG[C/G]AGAGCACTAGGGCCC | 58513 |
rs140895469 | snp | A/G | 0.0017452 | 0.0294882 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392329 | AAGGAAGGGTTTTTC[A/G]TGAATGGATCCGAGG | 58513 |
rs140910653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446771 | CACGTCCGTGATGAC[A/G]TGCTGGAGCATTTTA | 58513 |
rs140940408 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453721 | CATCTCAAAAAAAAG[-/A]AAAAAAAAAATGACT | 58513 |
rs140962962 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448063 | GAAAAACATGGGCCT[A/C]GAACTAAAAGTCTTA | 58513 |
rs140970265 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458883 | CATCGTTTAACTACA[C/G]GGATGCGTCCTGAGA | 58513 |
rs140975552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389790 | GGTTGCAAGTTTTCT[A/G]TATTTTACATGAGAT | 58513 |
rs141039721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390270 | CCAGAGATCAAATGG[A/G]AATCTTTTATAATGA | 58513 |
rs141050242 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373233 | ACCGCCAGGCTCACA[-/G]GGGGTCGCATTTCAC | 58513 |
rs141062545 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415558 | AAAGTGCTCTTTAAA[C/G]TGAAGGACCTGACAT | 58513 |
rs141071663 | snp | A/G | 0.000268777 | 0.0115895 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425203 | GCTGGCAGGCAGGAC[A/G]GGGACGGCGCCAGGG | 58513 |
rs141116025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361228 | GGATTTCTTTTTTCA[C/T]TGGAGCTGGTAACTG | 58513 |
rs141199606 | in-del | -/GGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375872 | CAGGAGGAGAGAGGC[-/GGG]GGTGTTCTAAAAATA | 58513 |
rs141199680 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398673 | GTTTTTAAAGGTAGG[A/C]TCTCACTACGTTGCC | 58513 |
rs141209515 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466591 | ATACTCACTGAACGA[A/G]CAGTGTGATCTACAA | 58513 |
rs141250750 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362370 | ATACACTGCAAGCTT[C/T]TAACAGTAAAAAAAA | 58513 |
rs141284425 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452077 | CCAGGAGGCGTAGGT[C/T]GCAGTGAGCCAAGAT | 58513 |
rs141303262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429713 | CCCTGTCACCTGGCT[A/G]CTGCTGAGCCCCTGA | 58513 |
rs141348200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377022 | CCACACAGGGTCCCA[C/T]GGCATCTGCTGCTAC | 58513 |
rs141367682 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372227 | ACCGGAACTCTCCCT[C/T]GAGGAACCTCTGCAG | 58513 |
rs141373053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442552 | CTGGAGAGCTCAGAG[A/G]GAAAGGACACTCTAT | 58513 |
rs141472194 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379085 | GAGGCGGGCAGATCA[C/T]GAGGTTAGGAGATCA | 58513 |
rs141506231 | in-del | -/GGGGGGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379858 | CACACAAAAGTGGCT[-/GGGGGGGG]GTCTAAGACTGTAGA | 58513 |
rs141537729 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449049 | GAGGCCAAAGCAGGA[A/G]GACTGCTTGAGCCCA | 58513 |
rs141557327 | in-del | -/GA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367970 | AATAAACATGAGAGT[-/GA]GAGAGAGAGAGAGAG | 58513 |
rs141558471 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359468 | ACAATTAAGGGTCCT[A/G]TCTTCACTCAACCCA | 58513 |
rs141566680 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431734 | AGGATCAGTGTTTGA[A/G]GTGATGGATATGCTA | 58513 |
rs141581841 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373269 | TCCTCACTCAGCCAC[A/G]CTGGGACCCACGCAT | 58513 |
rs141588071 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469078 | GGAGGGAGTGGGCAA[C/G]TAGGAAGTAGAATGG | 58513 |
rs141592604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454138 | TTCGCTGTTTTCCCC[C/T]CTTGAGGGCACAGAT | 58513 |
rs141594507 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413159 | CATCCGCAGGGCCAT[C/G]ATACTGGCCAAGCTC | 58513 |
rs141616063 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452840 | CTCGCTCTGTCCCCC[A/T]AGCTGGAGCGCAGTG | 58513 |
rs141623349 | in-del | -/AT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445429 | TTGATCTAATTACAC[-/AT]ATGTCAGGTTTTGCA | 58513 |
rs141632584 | in-del | -/AC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368254 | ATCCTACACAATGGG[-/AC]ACACACACACAAGCA | 58513 |
rs141633356 | snp | C/T | 0.111576 | 0.20818 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451808 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 58513 |
rs141651066 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423216 | AGTTCAGGGGTTTCA[C/T]GTAGCAAGTATGTGT | 58513 |
rs141674499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460772 | AAGAACATGCGCCTA[C/G]GCCAATCGTGTCTGG | 58513 |
rs141695393 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403850 | CAATCGGTTCAGCTC[C/T]GACTTGGCTCGGTTC | 58513 |
rs141757622 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419327 | AGCCGGGCATGGTGG[C/T]GCGCGCCTGTAATCC | 58513 |
rs141813054 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422822 | AATTAGCCAGGTGTG[C/G]TGGTAGGCACCTGTG | 58513 |
rs141848098 | snp | A/G | 0.000198 | 0.00994791 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417991 | GGGACCATGTCCGGC[A/G]AGAGGACTTGAGGAG | 58513 |
rs141852338 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419465 | CTGTCTCAAAAAAAA[A/T]AAATAAAAAAATGAG | 58513 |
rs141869509 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416560 | GAAGATCACTTGAGC[A/C]CAGGAGGCAGAGGCT | 58513 |
rs141885889 | in-del | -/A/AA | 0.180881 | 0.240541 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362000 | TGGAAAGTTTAGGAG[-/A/AA]AAAAAAAAAAGGAGA | 58513 |
rs141905143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440689 | ATGAAAGATGGCTCC[A/G]AGTGTTTAAAAGACC | 58513 |
rs141950729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398169 | TTAAGACAAGCCACC[A/G]GTCTGGGCTGTGAAT | 58513 |
rs141987376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395872 | ACTGCTTGAACCCAG[A/G]AGGTGGAGGTTGCAG | 58513 |
rs141988301 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439535 | CTCTACAAAAAAAAT[A/T]ATAAAAATTAGCCAG | 58513 |
rs141992490 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464889 | ATCGAGACCATCCTG[C/G]CTAACCAGTGAAACC | 58513 |
rs142000971 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396911 | AGTCATCACATTCAC[A/G]GTGACGAAGTAGAAC | 58513 |
rs142013211 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407831 | CCGTCAGGCCACAGC[A/G]CAGCCAACCCCTGTG | 58513 |
rs142016766 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435394 | TAGGGCAGGCAGCCC[A/G]TAAAAGGGGCCATGA | 58513 |
rs142126423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380418 | GATGCAGCCGTCTAG[A/G]CTTCTAGCGTTTACT | 58513 |
rs142214922 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402688 | CTGGGACTACAGGTG[C/T]GTGTCACCACCTATA | 58513 |
rs142217610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433704 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 58513 |
rs142220637 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375714 | TCTGTATCTGCTCAA[C/G]AGTTCACAGAAAATC | 58513 |
rs142223385 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400988 | CAGATGGGGAAAGTA[C/G]GAGCCGGGTTGTGAG | 58513 |
rs142228739 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446117 | AAGGAGAAGGACAAG[C/T]TCACATCCTTCTGCT | 58513 |
rs142236948 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470643 | AATCACCGGGTTTTA[C/G]CACTGTTAACTTAGT | 58513 |
rs142246638 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443642 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 58513 |
rs142250956 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400031 | ATAGACAAGAAATAA[A/C]TATGGCTTTAAGAAC | 58513 |
rs142308588 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364525 | CCAGCCCGCAGACCC[C/T]GGGCTGGTTCCGCTG | 58513 |
rs142320391 | snp | A/G | 4.94499e-05 | 0.00497217 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404617 | CCTGGCACTTCTGCC[A/G]GACGTCGCTCAGCAT | 58513 |
rs142338399 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380918 | CAGAGATATGGCTGC[C/G]TCGGACCTTGTGTAG | 58513 |
rs142344839 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463019 | CCTGGGTGCCCAGCT[A/G]CAGTTGAGCTGACCT | 58513 |
rs142361041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421200 | GAATAAAGGACGCCA[A/G]ACACAGCGGAAGCCT | 58513 |
rs142382276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420397 | TTCAGAGTCATAAAG[C/G]GGACACTGTGTTTTG | 58513 |
rs142398856 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417106 | GGGGCTACTGAGCTG[C/T]GACCTGCCTGAGACC | 58513 |
rs142410927 | in-del | -/AC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437710 | TACACACATGCACAT[-/AC]ACACACACACACACA | 58513 |
rs142487506 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449873 | TGACTCTCCAGAGAA[C/T]TATGCTGAATGACAA | 58513 |
rs142506606 | snp | A/C/T | 3.29458e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395423 | CGGATGCAACTCTTG[A/C/T]GTGTTGTTGCTAAAT | 58513 |
rs142544986 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413783 | CTTACCTGCACCTCG[C/T]TGGTTTTCTGTCTGA | 58513 |
rs142589876 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383540 | CTGCCAGTCCCAAAC[C/T]GTGTCACAGCGTGGC | 58513 |
rs142631693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386106 | GGAGTGAAAGTGTTA[A/G]CTGCGGGGGAGCTCT | 58513 |
rs142651319 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455481 | CAGGCTTCCTGCCTC[A/G]ATGCACTGCCCTGTG | 58513 |
rs142666761 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397960 | ACACTGGCATTCCTG[C/T]GTAGGACTCACAAAC | 58513 |
rs142669068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382252 | CCTAGCTCCAGAATG[C/G]CCGCGTCATTTCCGA | 58513 |
rs142671737 | in-del | -/C | 0.212728 | 0.247206 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357861 | GGCACAGATAAGCAT[-/C]CCCCCCCGCCCCAGT | 58513 |
rs142681211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465739 | TCTCTACCTTTTAAT[G/T]AGATGAGATTAAAGT | 58513 |
rs142721497 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473816 | ATACAAAAATTAGCC[A/G]GTTGTGGTGGTGGGC | 58513 |
rs142757044 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396495 | TTTTGAACTCCTGAG[C/T]TCAACTGATCCTCCC | 58513 |
rs142762374 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464858 | GGAGGCCAAGGCGGG[C/T]AGATCACAAGGTCAG | 58513 |
rs142833411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408613 | TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCACTC | 58513 |
rs142834272 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389196 | AAGTGACTCAAGCCT[C/G]TGATCCCAGCACTTT | 58513 |
rs142836018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469977 | TAACCCATGGTGTAG[A/G]TTTTCACTCGAGAGC | 58513 |
rs142859114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429573 | TCAGGCCTCACCAGC[C/T]CACACAGCCAAGAGC | 58513 |
rs142861153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400224 | TGCCTGTAATCTCTG[C/T]TACTCGGGAGGCTGA | 58513 |
rs142945378 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383342 | TGCTAGCTCTCCCTC[C/T]CTCTGCTCACAGTGA | 58513 |
rs143012439 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427054 | TCACAGGAAAACTTC[C/G]TGCAGCAGTGGGAAG | 58513 |
rs143031965 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464821 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 58513 |
rs143068227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363830 | ACTTTTCTCTCAACC[A/G]GCAGTTCTGGGCCAG | 58513 |
rs143071089 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361801 | AAGTCTGCAAAGCCC[A/G]AGGCAGAGGCCTTAG | 58513 |
rs143082862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434945 | GTCCTCTTTTTTTTT[C/T]TTTTTTTCTTTTTTT | 58513 |
rs143106495 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422754 | CTGAGGCCAGGAGTT[C/T]GAGACCAGATTGGCC | 58513 |
rs143149888 | in-del | -/AG | 0.104504 | 0.2033 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435699 | CGGACTTGCTGACTC[-/AG]TGCCTTCAGAAGCCC | 58513 |
rs143206632 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403237 | CACGAGAAGCCAGCG[-/C]CCCCCCCCTGGACTG | 58513 |
rs143207355 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414425 | TTTTTTTTTGAGACA[C/G]AGTCTCGCTCTGTCA | 58513 |
rs143244127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410568 | TGTTCCTAGCAACAA[C/T]ATTTGCAAAGCCAAA | 58513 |
rs143261397 | snp | C/T | 4.94344e-05 | 0.00497139 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392381 | GTTTCTTGAAGAAGT[C/T]GTCAGTGGCAGAGCC | 58513 |
rs143309058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417739 | AAAATTGTCCCTTTA[A/G]TACACAGGGTGAGGT | 58513 |
rs143327127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463767 | ATGGAAAAGGTGTCC[A/C]TCTCCACCAGTGGTA | 58513 |
rs143347595 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467899 | TACTCTATTTCTGTG[G/T]GTCTTGGTTTCCTCA | 58513 |
rs143382244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372381 | GACAAGCAGCTCCCA[C/T]GGAATTTGAAAACTG | 58513 |
rs143392539 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416923 | CAAAGCCCTCGTTTA[A/C]ACATGAGGAAACTAA | 58513 |
rs143401905 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412344 | ATCTCTACTAAAATA[C/T]AAAAAATTAGCCAGG | 58513 |
rs143422423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391910 | ACCGTGCAGGGTGGC[C/T]GGGTCCATGCGAGCA | 58513 |
rs143484833 | snp | A/G | 0.000115434 | 0.00759631 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392288 | GCTCTCCCGGGCAAC[A/G]TCCCACCCCACTCAC | 58513 |
rs143490617 | snp | C/T | 3.3054e-05 | 0.00406521 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417613 | CGCCAGTAAACTCCC[C/T]GGAGCCGAGAGAGCC | 58513 |
rs143515806 | snp | C/T | 6.6379e-05 | 0.00576065 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441909 | TCCCAAGGATAATGT[C/T]CGAGAGGCCAGACTT | 58513 |
rs143525693 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431423 | ATTCTCCTGCCTCAG[C/T]TTCCCGAGTCGCTGG | 58513 |
rs143525777 | snp | C/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388584 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCA | 58513 |
rs143534370 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455456 | GCTGGAGAAAAAACA[C/T]TGCCTGCAGCAGGCT | 58513 |
rs143570436 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357501 | GATCAGATTGGCAGC[A/G]TCTGGATATTTCACG | 58513 |
rs143635462 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397370 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 58513 |
rs143671746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445641 | TCTGTCACTGGCCCC[C/T]GTGCAGAGACCTCTT | 58513 |
rs143673087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394708 | GTTTTCCAGGTACTT[C/T]CATGATCATTACTAG | 58513 |
rs143717138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381726 | CTTAGCTTTAAAATG[A/G]GCCGTTTAGGGTCGG | 58513 |
rs143789982 | snp | A/G | 1.6659e-05 | 0.00288604 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425159 | CTGCCGTGGGACGGC[A/G]TGGAGCGGAGGCTGT | 58513 |