SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs143838791 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447482 | AAGTATTACAGGGCC[A/G]GGCACTCTGGCTCAC | 58513 |
rs143865958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378714 | CGGTGAGGCACAGGG[A/G]AGCCAGGGTCTCCAT | 58513 |
rs143896959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374683 | TTTCCATGAAACACT[A/G]AAAATGAAGCTTTGC | 58513 |
rs143916239 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413679 | TCCATCCAGGGCAGA[C/G]CCCTGCCCTTCCCCA | 58513 |
rs143952641 | in-del | -/A | 0.210909 | 0.246925 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429069 | AGACATCTTAGAAAA[-/A]GACAGCTTTGATTGA | 58513 |
rs143967181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420224 | CCTCTGAGTTCCTTC[C/T]TTTGATCCAGGTGGA | 58513 |
rs143998806 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359188 | AGAACGTCCACGCTG[-/A]AAAGAGTCACGCTGC | 58513 |
rs144013205 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379837 | ATCTGAGGCTCCAGC[A/G]TCTAGTCACACAAAA | 58513 |
rs144033570 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419745 | TCAAAGAACATTGCT[C/G]ATAAATGCCTAGTTA | 58513 |
rs144033744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376365 | GTCTGGCCAACTGGC[C/T]GCCGGCCTAACTCTG | 58513 |
rs144042862 | in-del | -/T | 0.214843 | 0.247516 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432980 | GGCTAGTTTTTTGTA[-/T]TTTTTTTTTCAGTAG | 58513 |
rs144072559 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429927 | TGCCGTGCACTGCAG[G/T]GTGGTGAGCAGCATT | 58513 |
rs144177040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414076 | CCTCTAAAAGCAGCG[C/T]GCTTTCTCCACCTGG | 58513 |
rs144224124 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462458 | TAGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 58513 |
rs144226662 | in-del | -/GGGGGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403339 | AACACACCAGTGGCT[-/GGGGGGG]GTGGAGGATGACGTC | 58513 |
rs144235275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359678 | CCAGACTGGGTAGTA[A/G]AGTGAGACCTTGTCT | 58513 |
rs144278486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356264 | TATTTCTACCTCCAG[C/T]CATGCTCCAGAGAGC | 58513 |
rs144280225 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404394 | TATACAACCTGACTT[C/T]TAGGAGTACAGGGGG | 58513 |
rs144301162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444371 | CCTCGTGCTTGGAGG[C/T]AGTGACACCATTCCT | 58513 |
rs144312610 | snp | C/T | 0.000535977 | 0.0163616 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361940 | ATGGATCGGGGGCCT[C/T]GGGAAAGTCTGCGGA | 58513 |
rs144312760 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465308 | GACCTGAGCCTCTGC[C/T]GTGGGCCGGGCCTGG | 58513 |
rs144315208 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359337 | CCAGAAACCACCAGC[C/T]GATCGGCTGAGCCCC | 58513 |
rs144385597 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399130 | GGCCTGCAATCACTT[A/T]CTCAGGAGTCATTGG | 58513 |
rs144455965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366552 | GTTTTGCTCTGTTGC[C/T]GAAACCGTTGTTATT | 58513 |
rs144494215 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406198 | AAAAACATCCTGGTG[C/T]TTCCCTGCCTCGATA | 58513 |
rs144499989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360809 | TAGAGATTATCAAGA[C/T]GGCTCAGAAACAAAT | 58513 |
rs144511295 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383082 | GAGCTGCAAGGTCAG[G/T]GTTGAGCTCAGAATG | 58513 |
rs144538184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401125 | TGATGATGACGGGCC[C/T]GGGGGCGGCTATGGA | 58513 |
rs144623166 | snp | C/T | 0.00078905 | 0.019847 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361784 | CTCAACTTACAGAGG[C/T]GAAGTCTGCAAAGCC | 58513 |
rs144629979 | snp | C/T | 1.65438e-05 | 0.00287605 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441968 | CCCACCCTCCCTGTG[C/T]ATGCCGGATCGACCT | 58513 |
rs144643552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379567 | GAGGTATGGCTGCCT[C/T]TGCCTCCAGCATCTA | 58513 |
rs144649150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449657 | CCTGGGCATTTACCC[A/G]GGAGAAATGAAGAGT | 58513 |
rs144659206 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429366 | CATGCCAGCCTTCCT[C/G]GATGGGCACACTGCC | 58513 |
rs144682246 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439622 | CTTGAACCCAGAAGA[C/T]CGAGGCTGCAGTAAG | 58513 |
rs144692903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407181 | ATGTCAGCGTCTGCA[A/G]TGACAAAGGTGCTCA | 58513 |
rs144716290 | snp | A/G | 0.000565921 | 0.0168119 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425137 | TGTGCTGTTGAGGCT[A/G]CTGACGCTGCCGTGG | 58513 |
rs144736649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394933 | AGAAGCTTAAAAGGC[A/G]TTCCTGCTGGGTGCG | 58513 |
rs144760922 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396526 | ACCTCAGCCTCCCAA[C/T]GTACTGGGATTATAG | 58513 |
rs144768974 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424186 | GGGTGGCCCTTGGGA[C/G]GCCCAGACAAGAGCA | 58513 |
rs144835204 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434738 | GGAGGCCCTGGCCCC[A/G]GGTCTTGTCCTTCGT | 58513 |
rs144869432 | snp | C/T | 4.94482e-05 | 0.00497209 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413816 | GCCTCTTCCTTTTCT[C/T]GAATGTCTTGTTCCA | 58513 |
rs144874769 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459524 | GAAGGTGCAGTTGGT[A/C]GTGGGGAGCGGGCAG | 58513 |
rs144882765 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390319 | AGAAAGACACAACAA[C/T]CATAAACACCTATGC | 58513 |
rs144887012 | snp | A/T | 0.000115591 | 0.00760145 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417983 | CCGAAGGCGGGACCA[A/T]GTCCGGCGAGAGGAC | 58513 |
rs144895844 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406670 | CTAGGGGCTCCAACA[C/G]CTTTGGCCTGCCCAG | 58513 |
rs144906547 | snp | A/G | 5.0653e-05 | 0.00503229 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425212 | CAGGACGGGGACGGC[A/G]CCAGGGAACACAGTC | 58513 |
rs144908454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389003 | CCTGTAATTCTATCA[C/T]TTTGGGAGGACGAGG | 58513 |
rs144915745 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456148 | GAGGTTGCAGCGAGC[C/T]GAGGTTGTGCCATTG | 58513 |
rs144918680 | snp | C/T | 3.80243e-05 | 0.00436012 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386138 | CTACTGCCCAAGGAA[C/T]AGTCAGGAAGAAAAA | 58513 |
rs144923331 | snp | A/G | 0.00235509 | 0.0342345 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16440901 | TTCTGGATCGGCCAA[A/G]TCCCATATCTGCGGA | 58513 |
rs144946594 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383641 | TCTGCCCAGGCTCAT[C/G]TGTGTAAACACACAC | 58513 |
rs144959343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453599 | GCGCCTGCAGTCCCA[A/G]CTACTCGGGAGGCTG | 58513 |
rs144985965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360607 | TAAACATTAGCCTTG[C/T]GTGGTGTTGCACGCC | 58513 |
rs144990448 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459412 | AGGGTGGAGGGATCA[C/T]GCTGTGCCCTCCTAG | 58513 |
rs145063792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389947 | AAAAAAACATTCAAA[C/T]AATTCAAAAGAAAGC | 58513 |
rs145127797 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405300 | AGAGCAAAAGGGAAT[-/G]GGTGGAGGCATCAGA | 58513 |
rs145156611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443143 | GCTGATGTAATAAGC[A/G]ATAAAAGTGAAGAAT | 58513 |
rs145177051 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438848 | TTTTTTAAAGCAGTC[A/G]TAAATACACACGGTT | 58513 |
rs145234973 | in-del | -/CACTAACACTAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464743 | TACACTAACACTAAC[-/CACTAACACTAA]ACTAACACTAACACT | 58513 |
rs145285990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441196 | CCGCAAGTGGCCAAG[C/T]GCGGTGGTTCACGCC | 58513 |
rs145289403 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370050 | CACATGTAACAAGAT[C/G]CCTGAGAACGCCGTG | 58513 |
rs145306253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436473 | AGGCTTTTCACAAAG[C/G]AATCAGAACATCAGG | 58513 |
rs145310108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367105 | CGCATTTCAGAAAAG[A/G]GGATGGAAATCATGA | 58513 |
rs145323635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458384 | CACACCAACACAGAA[A/G]AGCAAATGCACAGCA | 58513 |
rs145351677 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412283 | GAGGCAGGCAGATCA[A/C]GAGGTCAGGAGATTA | 58513 |
rs145367427 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371659 | ACCGCAACGCAGGGC[C/T]GCGCTGGCAGGAAGT | 58513 |
rs145407420 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385450 | CATCATTCACGGTCA[C/T]CAGAAGAGTGACAAG | 58513 |
rs145409955 | in-del | -/ATAAATAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433963 | GCAAGACTCCATCTC[-/ATAAATAA]ATAAATAAATAAATA | 58513 |
rs145429616 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462374 | CAGAATCAGGGAAGT[-/G]GGGGGGGAGGGCATG | 58513 |
rs145430648 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451212 | TGCCTCGGCCTCCCA[A/C]AGTGCTGGGATTACA | 58513 |
rs145452438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369248 | TCAAAGCTGTGTCAA[A/G]CAGCACAGCCCCGGG | 58513 |
rs145472563 | snp | A/G | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441498 | GCCGGGTGTGGTAGC[A/G]TGTGCCTGTAATCCC | 58513 |
rs145497697 | in-del | -/G | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449083 | GTTCCAGACCAGCCT[-/G]GGCAACATAGTGAGA | 58513 |
rs145546214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397588 | GGGCATTTGGGAAAA[C/T]GGAGTTTTCATACCA | 58513 |
rs145558313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426653 | CAAAAACAGAACAAC[A/G]ACAACAAAAAAACAA | 58513 |
rs145568283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436188 | ACCGTGTAAACATGG[A/G]ACGAAAGTGCTTGGG | 58513 |
rs145641260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424333 | TACCCTCCCACCCCA[C/T]CCCACCAGGGGCCAC | 58513 |
rs145675415 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462442 | AAGGTGGGTGGATCA[C/G]TAGAGGCCAGGAGTT | 58513 |
rs145679743 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420768 | GAGTGCCCCAGCCCT[A/G]TGAAGTCGGCTGTGT | 58513 |
rs145683476 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404666 | CTGCTGGTCCATCTC[A/G]TCCAGGCGGTCTTGA | 58513 |
rs145707581 | snp | A/G | 0.000395746 | 0.0140612 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385186 | GAAGGACCCACTTCC[A/G]AAGGGATCTAAGGTT | 58513 |
rs145722647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398216 | GAGTGCCGCTTCCTC[A/G]GCCCCCACTTCAGGA | 58513 |
rs145781187 | snp | C/T | 0.00716266 | 0.059414 | | | GRCh38.p7 | 19:16422154 | GCTCAAAGTTCACAG[C/T]CCTGGGGCTGGGTCA | 58513 |
rs145868009 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395976 | ATCAAGGTGTGGTGG[C/T]GTGTACCTATAATCC | 58513 |
rs145870019 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437521 | AATGTGGATGGGGTC[A/T]CCTTGCGGAGGGATG | 58513 |
rs145871172 | snp | A/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395457 | AAGGCTTTATTTTTG[A/T]AAGGATCATCCTACA | 58513 |
rs145887251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416545 | TGGGAGGGTGAGTGG[A/G]AAGATCACTTGAGCC | 58513 |
rs145893503 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407532 | GGTTTCACCATGTTG[A/G/T]CCAGGCTGGTCTTGA | 58513 |
rs145901156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434585 | AGTGAAAATGGCCAC[A/G]GACCCATCATCACCC | 58513 |
rs145911537 | snp | A/T | 0.0663309 | 0.169604 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473749 | GGATCACCTGAGGTC[A/T]GAAGTTTGAGACCAG | 58513 |
rs145912740 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402753 | AAAATACAAAAAAAA[A/T]TCTGTATTTTTTGTA | 58513 |
rs145931807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382303 | AAGTTTCCCAAGAAG[C/T]CTCCTTGGGGACTCA | 58513 |
rs145966018 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379962 | TCTAGTCACATAGAC[A/G]CGGCTGTCTGAGGCT | 58513 |
rs146009121 | snp | A/C | 3.38221e-05 | 0.00411216 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361868 | TTCCACTAAACGGGT[A/C]CCCAAACCCCTTTTT | 58513 |
rs146020217 | snp | A/C | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403798 | GCTGGACTCGCCCAG[A/C]CTGAATGCTCTGCTC | 58513 |
rs146049687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435067 | TCGTGCCTCAGCACT[C/T]GTACCTCCCGAGTAG | 58513 |
rs146083535 | snp | A/T | 3.31592e-05 | 0.00407167 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377132 | CTGACCGCTGGGCGG[A/T]TTAGGCCGTGGAGGA | 58513 |
rs146103489 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470108 | GTGACCTGGCCAGGC[A/G]CAGTGGCTAACGCCT | 58513 |
rs146157602 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368916 | GGAGAGCAGTGGCCC[A/G]GGCGGGGCACCACTC | 58513 |
rs146173915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419611 | CTCCCGTGTAGCTGC[A/G]GCAGAAGCCATTACA | 58513 |
rs146202793 | in-del | -/GGAATACA | 0.0287284 | 0.116357 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416848 | AAGAGGATCCAGAGG[-/GGAATACA]GGAAGTGACTGCATT | 58513 |
rs146240362 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403901 | TAAGTCAGATTCCTG[A/G]GATTGGATTTGCGTT | 58513 |
rs146251234 | snp | G/T | 0.000131941 | 0.00812116 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417999 | GTCCGGCGAGAGGAC[G/T]TGAGGAGGGTCGATG | 58513 |
rs146271245 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382029 | CGGGCAATAAAACCA[A/C]ACTCAGCCTGGACGT | 58513 |
rs146273418 | snp | A/T | 0.078151 | 0.181571 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451537 | TTATTTTATTTTTTT[A/T]ATTTTTTTTGAGATG | 58513 |
rs146292305 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469389 | ACCGGGGTTAAGGAC[A/G]GAGGGGCCACCGGTA | 58513 |
rs146294582 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400091 | CCTGTAATCCCAGCA[C/T]TTGGGGAGGTCGAGG | 58513 |
rs146392606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362767 | TGCCCGCCTCAGCCT[A/C]CCAAAGTGCTGGGAT | 58513 |
rs146404081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359548 | AAACTGGGGTATTTG[C/T]AGTGGGAAAAGTGAT | 58513 |
rs146434754 | in-del | -/G | 0.0283406 | 0.115616 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364761 | GTCCACTGGAGCAGA[-/G]AGGGGCTCCCTAGGG | 58513 |
rs146462390 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376671 | CCAAGCAGCGACTCC[C/T]GCCACCCTCACCCCC | 58513 |
rs146465644 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446716 | GGGCTGTGCACCGGA[A/C]CACAGGACAGCCTCA | 58513 |
rs146481830 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390080 | CAAGGCAGGGACTTC[C/T]GACTGGATTTTAAAA | 58513 |
rs146492800 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430429 | GCAACCAAGGTGACT[A/T]CCCAACCACCCTGAA | 58513 |
rs146551807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378760 | CAGCATATCTCAGGC[A/G]TCTGAGGGAAGGGGC | 58513 |
rs146585116 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356461 | GGATTACAGGCATGC[A/G]CTACCATGCCCAGCT | 58513 |
rs146590932 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429620 | TATCCCAGTCTTGTC[C/T]CTATGGCTACCACAG | 58513 |
rs146596383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372012 | AGACACCTGCTGGTT[A/G]TTTAATACCTTGATA | 58513 |
rs146599765 | snp | A/G | 0.000116074 | 0.00761731 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441979 | TGTGTATGCCGGATC[A/G]ACCTGAAATGGGAGA | 58513 |
rs146602189 | in-del | -/ATAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433962 | GCAAGACTCCATCTC[-/ATAA]ATAAATAAATAAATA | 58513 |
rs146720928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426368 | AACCAGGCATGGTGG[C/T]TCATGCCTGTAATCT | 58513 |
rs146721237 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465481 | TGAGGTCAGGAGTTC[A/G]AAACCAGCCTGGGCA | 58513 |
rs146732940 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464057 | AGCTGCCGGTAGCAG[C/T]GCCTGATCCAGCCTG | 58513 |
rs146779568 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356118 | CAAAGAAACCAGCCA[C/T]CCCGCCCCACGCAGA | 58513 |
rs146800442 | in-del | -/G | 0.0275645 | 0.114116 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434711 | GGATCTGGGAGCCAA[-/G]GTCCTCAGGAGGGAG | 58513 |
rs146831227 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394888 | CACTGTATCTTGATG[C/T]CTTGGCTCTCTGGTT | 58513 |
rs146919353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434016 | ACAGACACACATTCC[C/T]ACATTCAGCACAATG | 58513 |
rs146955382 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471371 | AAGCGCATCAGGCGA[A/T]TTTGAGGACACAGAG | 58513 |
rs146955602 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431013 | GGAGTCCAAGGCAGG[C/T]GGATCACCTGAGGCC | 58513 |
rs146956820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358790 | ATTCATTCATTTACC[A/G]ACAATGAAATTGTAT | 58513 |
rs147059646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454780 | TGGACCAGGAAGGTC[A/G]TCAGAACACAGAATC | 58513 |
rs147069576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452002 | AAATTAGCTGGGTGC[A/G]GTGGCGTGCACCTGT | 58513 |
rs147174754 | snp | C/T | 0.000181379 | 0.00952138 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392291 | CTCCCGGGCAACGTC[C/T]CACCCCACTCACCTT | 58513 |
rs147180882 | in-del | -/ACACTAACACTA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464748 | TAACACTAACACTAA[-/ACACTAACACTA]CACTAACACTAACAC | 58513 |
rs147183654 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448660 | ACCAGCCTGGCTAAC[A/G]TGGCTAAAAATACAA | 58513 |
rs147185347 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405890 | CTGAAATAGCACAAC[A/G]GGCATTGTGACAAGC | 58513 |
rs147195288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445705 | AAGAGCCCTCTGTAT[G/T]CTGAGAGCAGCCTCT | 58513 |
rs147243735 | snp | A/G | 4.99954e-05 | 0.00499952 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425166 | GGGACGGCGTGGAGC[A/G]GAGGCTGTCTTTTGG | 58513 |
rs147282454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374740 | TCCTCCTCAGGGCCC[A/C]GCAAATACGGCACTG | 58513 |
rs147291095 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388718 | TGTAGTCCCAACTAC[A/T]CGAGAGGCTGAGGCA | 58513 |
rs147397479 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369884 | GTGTCAGCCCCATCC[C/T]CTGGGGGGATTTCCA | 58513 |
rs147407581 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408821 | AGGAGAGGCAGATAG[A/G]TCAATGGGATAGAGC | 58513 |
rs147490918 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408343 | CAAAATTCATATGGG[A/G]CCAGGCACGGTAGCT | 58513 |
rs147500032 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464859 | GAGGCCAAGGCGGGC[A/G]GATCACAAGGTCAGA | 58513 |
rs147510567 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461162 | TACAAAAATTAGCCG[C/G]GCGTGGTGGCAGGCG | 58513 |
rs147558797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436478 | TTTCACAAAGCAATC[A/G]GAACATCAGGGAGGA | 58513 |
rs147654006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441277 | GGAGTGCGAGACCAG[C/T]CTGGCTAACACAGTG | 58513 |
rs147722510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383460 | CACCGTGTGGCCAAC[A/G]TTTTCTGCTTTCGGG | 58513 |
rs147722989 | snp | C/T | 1.65488e-05 | 0.00287647 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392432 | TGAAAGGGTCCCCTC[C/T]AAATGGATCTAGAAG | 58513 |
rs147729480 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358986 | AAGAGGTTTCCCGGG[-/A]AACAGCCACACACGC | 58513 |
rs147758033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380897 | TGGGCTATTTGCGTC[C/T]CGTCACAGAGATATG | 58513 |
rs147758261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424419 | GAGGTGGGTTATGAC[A/G]CTGGGTGACCTGTGC | 58513 |
rs147765247 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471224 | AATGCAGCGCTCCCA[C/G]CACCTGACCCAACGC | 58513 |
rs147767567 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401148 | GCTATGGAAACCACC[C/T]CATTACGAGTCCACG | 58513 |
rs147775088 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466392 | CTCCATCATCAGATC[A/G]GAACCTGCCCTGCTC | 58513 |
rs147826858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367041 | CGCCAGGGTTTTATA[C/T]TTTTTTATGGCTCCA | 58513 |
rs147863066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361062 | TCCTTGAAGCGACGG[C/T]ATGTTACAATCTGGA | 58513 |
rs147866871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383690 | GGGATCTGCTGCGCC[A/G]CCAGGGCACGCACAC | 58513 |
rs147870859 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453692 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 58513 |
rs147930036 | snp | C/T | 0.000494413 | 0.015715 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413820 | CTTCCTTTTCTCGAA[C/T]GTCTTGTTCCAGTGA | 58513 |
rs147938566 | in-del | -/CT | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443233 | GCAGGGAAAAGAGGA[-/CT]CTATCTTGGGGGCAG | 58513 |
rs147964227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389073 | AGCCTGGCCAACATG[A/G]TGAAACTCCATCTGC | 58513 |
rs147967357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458222 | GCTGTGGGTGACAGC[A/G]TCAGCCTCCTAGTGC | 58513 |
rs147985616 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460345 | TTTTCTTAAAAAAAA[A/T]ACAATTTTACACACA | 58513 |
rs147985943 | snp | A/C | 6.62954e-05 | 0.00575702 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417625 | CCCCGGAGCCGAGAG[A/C]GCCTGAACTGTCCTA | 58513 |
rs148029183 | snp | C/T | 0.000209311 | 0.010228 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418143 | ATTACACATCACAGG[C/T]GCCGACTCAGCCTGA | 58513 |
rs148037616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455468 | ACATTGCCTGCAGCA[C/G]GCTTCCTGCCTCGAT | 58513 |
rs148079639 | in-del | -/TG | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375493 | gtgtgtgtgtgtgtg[-/TG]CTTCTGCTCCCATCT | 58513 |
rs148081764 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447692 | TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAGC | 58513 |
rs148154346 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434752 | CGGGTCTTGTCCTTC[G/T]TCCTAGCTGCTGCCT | 58513 |
rs148177246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407719 | AACCTTGCTGGGTAA[G/T]TTTTTGCACATAGTT | 58513 |
rs148188074 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387416 | GTTTGAGACCAGCCT[A/G]GTCAATATGGTAAAA | 58513 |
rs148198133 | snp | A/G | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427663 | TTAGGAGGCAGAGGC[A/G]GGCAGATCACTTGAG | 58513 |
rs148227808 | snp | A/G | | | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395399 | GGGGTCTTCTGTCTG[A/G]AAAGGATCCGGATGC | 58513 |
rs148232087 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368341 | AACAGGGGACACACA[A/T]GCACAAGCATCATTG | 58513 |
rs148242333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382001 | TCTACCCTCTGTGTC[A/G]CGCAATAGGACCCGG | 58513 |
rs148245403 | snp | A/G/T | 0.0166325 | 0.0896639 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452071 | TTAAACCCAGGAGGC[A/G/T]TAGGTTGCAGTGAGC | 58513 |
rs148294866 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412835 | GGAGCCGGGACCAAG[A/G]CCACGGAGCTTGCAG | 58513 |
rs148354438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431611 | CGGGCCAGAAGGAAT[A/G]AGTTCTAAAGTTCAA | 58513 |
rs148365309 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468449 | CGCCTGGTTTCAAGC[A/G]ATTCTTGTGCCTCAG | 58513 |
rs148388592 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372675 | AGAAGCCTGCGTCCC[A/G]GTCCCTGTGCCGCAG | 58513 |
rs148399892 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449844 | AACAGCTGACACATA[C/T]GCAATAATCTGGATG | 58513 |
rs148493117 | snp | A/C | 0.000176882 | 0.00940263 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361818 | GGCAGAGGCCTTAGA[A/C]GGTTTAGCTGCAGAG | 58513 |
rs148508142 | snp | A/G | 8.32924e-05 | 0.00645285 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425149 | GCTGCTGACGCTGCC[A/G]TGGGACGGCGTGGAG | 58513 |
rs148516700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429434 | TCTAAGCAGATGCCC[A/G]TGGCTCTATCCATGA | 58513 |
rs148521148 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439641 | GGCTGCAGTAAGCAG[C/T]GATCGCACCACTGCA | 58513 |
rs148523753 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369215 | CAGGCACCAGCCCCG[C/T]GCGCACTCTGCCTTA | 58513 |
rs148558060 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452916 | ATTCTCCTGCCTCAG[A/C]CTCCCGAATAGCTAG | 58513 |
rs148679556 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375450 | AGCTGTGTGCATGCA[C/T]TGTGATTATGCATAT | 58513 |
rs148680953 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470591 | TTAACAGTTTACAGA[A/G]CACTTTCATGTCAGT | 58513 |
rs148723012 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364349 | CAGGAATGTGGCCCC[G/T]CTCCTTCCGACAGCG | 58513 |
rs148725343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462883 | AAAAGACAAAAGGAG[A/G]CACAGGCGCCCTCTT | 58513 |
rs148732757 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405703 | TGCATTTGTGCGAAC[A/G]GGAAGGGGAGGGTAT | 58513 |
rs148756051 | snp | C/T | 3.29674e-05 | 0.00405988 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404615 | ATCCTGGCACTTCTG[C/T]CGGACGTCGCTCAGC | 58513 |
rs148767967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420286 | TACATCATGTGTCAA[C/T]TGCAGCATGCATTAT | 58513 |
rs148777036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359354 | ATCGGCTGAGCCCCC[A/G]AATGCCGTGAACATG | 58513 |
rs148837145 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430980 | TGGCTCACGACTGTC[A/G]TCCATCCCAGCACTT | 58513 |
rs148841275 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441662 | AAAAAGTCCACAAGC[A/T]ATCAAGACCCCAAAA | 58513 |
rs148858396 | snp | C/T | 0.000825696 | 0.0203019 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417611 | CACGCCAGTAAACTC[C/T]CCGGAGCCGAGAGAG | 58513 |
rs148873865 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384823 | AGACGCCTGTGCCCA[A/G]CGCCTTCTCAAGTTT | 58513 |
rs148885009 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397930 | AGCACAACACCCTCA[C/T]TGAATTTGGCAGACA | 58513 |
rs148946982 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381604 | GGACCACACGACAAT[G/T]ATCACACCAAGTACG | 58513 |
rs148998992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446965 | ACTGAAACACATCTC[A/G]GTCTGAGTTCCTACT | 58513 |
rs148999885 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378398 | TGTTTCCAAGTCCTG[C/T]AACACTCAGGTCTCC | 58513 |
rs149019261 | in-del | -/ATAATAATAATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393078 | CTGCAGGAGCTGGAT[-/ATAATAATAATA]ATAATAATAATAATA | 58513 |
rs149042546 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368087 | CAGATGAGAGATACA[C/T]ACAAAAACAAAAAGA | 58513 |
rs149089646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360711 | TCTGATCGCGCCAAT[A/G]CAGACCAGGCTGGGC | 58513 |
rs149092629 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433383 | GTTATCCACCCACCT[A/C]GGCCTCCCAAAGTGC | 58513 |
rs149165219 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455176 | AGGCTGGAGTGCAGT[A/G]GCACGACCATAGCTC | 58513 |
rs149210508 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412318 | CATCCTAGCCAACAT[A/G]GTGAAACCCCATCTC | 58513 |
rs149216602 | in-del | -/ATAATAATA | 0.368324 | 0.220226 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393078 | CTGCAGGAGCTGGAT[-/ATAATAATA]ATAATAATAATAATA | 58513 |
rs149221319 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451241 | CAGGCGTGAGCCACC[A/G]CGCCCGCCCAGACTC | 58513 |
rs149277443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424145 | CTGGAAGTGGCTTCA[C/T]TCAAACCTGGCATGA | 58513 |
rs149317909 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449640 | CATGAACCAGCAACT[A/G]TCCTGGGCATTTACC | 58513 |
rs149327029 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391358 | TAGGGAAATTCTCAC[G/T]ACAGGTCTTAAGGAC | 58513 |
rs149367823 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408252 | AAGACAAAAATAACC[C/T]CAACAGTCCACGGAG | 58513 |
rs149380860 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418066 | AACGCGAATTGGTCT[C/T]TGCTTAACTTCCCCG | 58513 |
rs149412120 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362626 | CCTCCAGGGCTCAAG[C/T]GATCCTCCCACCTCA | 58513 |
rs149489744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457172 | TTCCCTAAAAACGAA[C/T]GTGTTTCCTTGGGAT | 58513 |
rs149531973 | in-del | -/ACACTA/ACACTAACACTA | 0.471578 | 0.115772 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464729 | GGCCACACATAAAAT[-/ACACTA/ACACTAACACTA]ACACTAACACTAACA | 58513 |
rs149537556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427008 | TTGTGGATGAAGAGG[C/T]ATCATGTCTGCAACT | 58513 |
rs149541509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452409 | TGAGATTATGCTACT[A/G]CACTCCAGCCTGGGC | 58513 |
rs149545861 | snp | C/T | 0.000131817 | 0.00811735 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403758 | TCGTCTTGCGTTGAC[C/T]TCAGGGACTTGATGA | 58513 |
rs149574362 | snp | C/T | 0.000395296 | 0.0140532 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403839 | TCCTCCTGCTGCAAT[C/T]GGTTCAGCTCCGACT | 58513 |
rs149585078 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444231 | GCAGAAAAAACTAGA[A/C]TAACATGAAAAAGCA | 58513 |
rs149625905 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467826 | GCAGGGCTCTGCGGC[A/G]GGAGGACGCAGGTGT | 58513 |
rs149627105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398889 | ACAGCCCAGAACTCC[C/T]GGGCTCAAGGATCCT | 58513 |
rs149655982 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441485 | AAAAAAAAAATTAGC[C/T]GGGTGTGGTAGCATG | 58513 |
rs149676682 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370913 | GGCCGTTTTAGGCTC[C/G]TTGGGACCCCCTCCC | 58513 |
rs149688701 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382884 | CCACGCAGAGGTAAG[G/T]TGCTTCAATTCAGGG | 58513 |
rs149707799 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435759 | TGGCACTTCGGGCTT[A/G]TTCTTTCTGACTGTG | 58513 |
rs149761676 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465058 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTTA | 58513 |
rs149782701 | snp | A/G | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385153 | CTGGCTGAAGTCGGC[A/G]AAGCCTTCAGCACTA | 58513 |
rs149799318 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360414 | TCACTGCCGTTGTAA[A/G]ATATTTATAGGTCAC | 58513 |
rs149806899 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459257 | TCTAAGATGACCCTA[G/T]GTTCCCCCAAATGAA | 58513 |
rs149851025 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416457 | CCTGGGCAACATGGC[A/G]AAACCCCATCTCTAC | 58513 |
rs149853402 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356088 | AGTGTGACCTTAACC[A/G]TGACCTCTGGGCCTC | 58513 |
rs149857110 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429017 | TAAGTTTAAAGGCTA[C/T]ACTTTAAACTTACCC | 58513 |
rs149867879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406491 | GTAGCCCAATGCTCC[A/G]AGCGATGCTCCCACC | 58513 |
rs149903707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446540 | CAACGCTAAAGGGCA[A/G]GTAATATTACTAGTC | 58513 |
rs149910805 | snp | A/G | 0.000198475 | 0.00995983 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436997 | AGGGCTGCTGGTGTC[A/G]TGCTGAGAAGAGAGA | 58513 |
rs149941603 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400402 | ATAAAGTCACACTGC[A/G]TGAGCTTCACATGGA | 58513 |
rs150016057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397525 | GGCCTCATTTCAGAG[A/G]TGTGACCTTCCTCAA | 58513 |
rs150023256 | in-del | -/GGAG | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406293 | TTGAGGGCTGGATCT[-/GGAG]GGGACAATCAGGGTC | 58513 |
rs150056826 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380534 | AGCCATCTAAGGCTC[C/T]AGCGTCCAGTCACAC | 58513 |
rs150061335 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451106 | CAGGCACCCACCACC[A/G]TGCCCGGCTAGTTTT | 58513 |
rs150079831 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466316 | CGGGAGGATGAACCA[A/G/T]GCAATCTATGATGTT | 58513 |
rs150119024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362449 | TTCACAACGTGGTAT[A/G]GTTATTCGGTGTGTT | 58513 |
rs150172585 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358611 | TCAGAAGCAAATAAG[C/G/T]GGTTCATTTCAGCAG | 58513 |
rs150176493 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430720 | ACTGACCAGATGCAC[A/G]ATGTGTGAGTGCCTG | 58513 |
rs150233580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402206 | AAACAACAGACAGCC[A/G]CCTGCACTTGGCTGG | 58513 |
rs150235060 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377707 | GCTGGCCGGTGTGGT[C/T]ACTGCCTTCAGTTAG | 58513 |
rs150238617 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472674 | AGACAAGAACCCACT[C/T]GTTGCCAGGTACAGT | 58513 |
rs150310027 | snp | A/G | 0.000989332 | 0.0222191 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402408 | ACCATGGGCTCCATC[A/G]AGCACCTGGTCATAC | 58513 |
rs150332818 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398729 | CAGGTGCAATCCCAC[C/T]ACTGAGCAGCGTGGG | 58513 |
rs150354249 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438897 | GTGGTTCACCACGAT[A/C]CCCTCGGCCTCGTTG | 58513 |
rs150366931 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439074 | GCTTGTTTTTTTTCT[-/G]TTTTTTTTTTTTTTT | 58513 |
rs150379742 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395706 | CCCAGCACTTTGGGA[G/T]GCCAAAGCAGGTGGA | 58513 |
rs150390626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373395 | AGCCTGGGGTAGCAA[C/G]AAAGGCAGAAAGGCT | 58513 |
rs150395990 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444032 | TCGCGCCACTGCACT[C/T]CAGCCCAGGCGACGG | 58513 |
rs150423243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384521 | AACCACACTGCCAGC[A/G]TCTGGAGAAGCCCTA | 58513 |
rs150433066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426138 | CAACCTTGACCCACC[C/T]TGACCCAGTGATGAA | 58513 |
rs150448450 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438073 | ATGGACTTATCCTGG[A/C]CAGGTGTGGTGGCTC | 58513 |
rs150499993 | in-del | -/T | 0.0777841 | 0.181223 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443411 | AGGGTCATTTGAAGC[-/T]TAAAAATAATGCCCA | 58513 |
rs150512248 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423505 | AGCCCAGGAGGTTGA[A/G]ATAGCAATGAGCCGT | 58513 |
rs150548268 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460907 | GGGCCTCATCATCAA[A/G]TTTTTTCGTGTTTCA | 58513 |
rs150549431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379350 | GTTCCTCCAAGAGCA[C/T]AGAAGAGAAAGATCA | 58513 |
rs150700483 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397073 | AAGATGGTCAAGTTT[A/C]TGTCTATTTTTCTTT | 58513 |
rs150705609 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464987 | AGGAGGCTGAGGCAG[G/T]AGAATGGCATGAACC | 58513 |
rs150714690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446207 | AGCAGTTGAGATGGA[A/G]AAACCCAGCAGAACC | 58513 |
rs150721574 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456861 | TGGGTGATTCAGCAC[A/G]GCCCCAGTCAGGTGG | 58513 |
rs150743061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387848 | TGAAGTTGAAAACAG[A/C]GCAGTAGAAATTACT | 58513 |
rs150833446 | snp | A/G | 0.00011536 | 0.00759387 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404624 | CTTCTGCCGGACGTC[A/G]CTCAGCATGTCTCGG | 58513 |
rs150860141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364536 | ACCCCGGGCTGGTTC[C/T]GCTGGCCTTGAGGAA | 58513 |
rs150863165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435498 | GGTTAAGATGGTAAA[C/T]GTTACATGATGTGTC | 58513 |
rs150923079 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410362 | GAAAAACGGGAAATG[A/G]GTAAGTGTTGGTGAG | 58513 |
rs150937497 | in-del | -/GG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366861 | TTATTTTTAGCGGCT[-/GG]GTATTTTTCAAACCT | 58513 |
rs150968520 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401567 | GAACAGCACCAAGAC[A/G]AAATGGGAAACTACA | 58513 |
rs150985484 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357538 | TGGTGGCATGAGCGG[A/G]AAGCAGGAGAGAGGA | 58513 |
rs150998989 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465793 | ATGATATCTAATAAC[C/T]AGGTATAAAAACAAA | 58513 |
rs151018069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370631 | GTACAGTGTGCCCAG[A/G]AAGGCAAATGCTTCT | 58513 |
rs151032688 | in-del | -/AAAA | 0.0869089 | 0.189476 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456200 | AAACCCTGTCTCAAA[-/AAAA]CAAACAAACAAAAAA | 58513 |
rs151038768 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389611 | TTTGGGTAAAACTAA[A/G]TGACTACTTTTTTCC | 58513 |
rs151041865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458450 | ATGGGAGGGCCGCCC[C/T]GCCCCCACCCCGCTT | 58513 |
rs151080568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415177 | AGCTTCCTTTGCTCC[A/T]TTTGCCCTGTGAGGA | 58513 |
rs151091013 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453318 | CTTTGTTGCCCAGGC[C/T]AGTCTCTAACTCCTG | 58513 |
rs151135043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376107 | AGCTGATGGAAAGGG[C/T]TCGGGGGCATGCCCT | 58513 |
rs151180212 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437527 | GATGGGGTCTCCTTG[C/T]GGAGGGATGAAAAAG | 58513 |
rs151197144 | snp | C/T | 0.000858723 | 0.0207032 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395501 | ACAGGACAGGGATTT[C/T]ATTATTTCTGAGTTA | 58513 |
rs151231980 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433737 | TTTGGGAGGCCGAGG[C/T]GGGTGAATCTGAGAT | 58513 |
rs151248319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425673 | ACCTGTACTTCAAGA[C/T]GTTCAGGAGTAGTCC | 58513 |
rs151285307 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463106 | GCAGACAGAATCTCA[C/T]GGTGCCCCAGCCCCA | 58513 |
rs151301323 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420512 | ATGACTCTGCGACAG[C/T]TAGTTCTCAGGCTCC | 58513 |
rs180672385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435604 | TCACCGGCAGACACC[A/G]CATGCTTTCACAGCT | 58513 |
rs180687099 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415000 | TCATGAGCCACAGCA[A/C]CCAGCCTTCTTTTAT | 58513 |
rs180687187 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451214 | CCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 58513 |
rs180997805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381725 | GCTTAGCTTTAAAAT[A/G]GGCCGTTTAGGGTCG | 58513 |
rs181005538 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357992 | GACAGTGCAGCTGAC[C/G]GGGACCTCACCCTCC | 58513 |
rs181020894 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404148 | CCCACTGTGGCTAAC[A/C/G]GAAGATCACTTTGGA | 58513 |
rs181068664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394742 | TGATTATTTTATCAA[C/T]CCTGTGAGGTGAGCA | 58513 |
rs181073612 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370167 | CCAGGAGCTCCCATG[A/G]TGGGGGACACTTTTG | 58513 |
rs181184506 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358759 | ACCATGTGCAGGACA[C/T]GCCTAGCCACTTCCC | 58513 |
rs181192197 | snp | C/T | 0.000395342 | 0.014054 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394036 | AATGCTTATTAGCTC[C/T]AGGGCACAGGATGCG | 58513 |
rs181196056 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405266 | GGACCCCAGGGTCGG[C/G]GGGTGTCGCACTCCA | 58513 |
rs181199241 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434831 | CAAAGATCAGTCTCA[A/C]CTGCCTCCAAGGAGC | 58513 |
rs181207375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425425 | ACAGGACACTCTGTC[A/G]GGACGCTCCCAAGCT | 58513 |
rs181207863 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382791 | AGGGTGGGGCCTCAA[C/G]TAAGAGTGCAGGCCC | 58513 |
rs181212913 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450859 | GACTCTTCCTTCAGA[A/T]CCTGAACATAGCCAT | 58513 |
rs181215855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414699 | CCAACACGCCTGGCC[C/T]TTTTTTGGTTTTGTT | 58513 |
rs181219192 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368253 | GATCCTACACAATGG[A/G]ACACACACACACAAG | 58513 |
rs181239038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375282 | TGCATGTGTGTTCAT[A/G]TGCAAACAGGTGCAT | 58513 |
rs181253226 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461135 | ACGGTGAAACCCCGT[C/G]TCTACTAAAAATACA | 58513 |
rs181265407 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444145 | GGAAAATAGCATAAA[G/T]ATCTGAAAGGGGAGA | 58513 |
rs181303840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400040 | AAATAAATATGGCTT[G/T]AAGAACCCTGACTTT | 58513 |
rs181324355 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410598 | AACATCTATCAATGA[A/C/G]GGATGGATGAGTAAA | 58513 |
rs181335898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364528 | GCCCGCAGACCCCGG[A/G]CTGGTTCCGCTGGCC | 58513 |
rs181343127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437418 | AGAATTCCATTGATA[A/G]GAAATGTCCAGAACA | 58513 |
rs181345883 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430561 | TAGGGCCCGGCCTGC[A/C]CATACTAAGCCCTCA | 58513 |
rs181348408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466589 | AAATACTCACTGAAC[A/G]AACAGTGTGATCTAC | 58513 |
rs181355517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447942 | AGAATCTGAGAAACA[A/G]ACACACACAGATCTG | 58513 |
rs181384170 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457352 | CAGGATGGAGGGCCA[A/G]TCCGCAGCCAGCAGC | 58513 |
rs181449584 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455738 | TCTGGAGATGAGGGT[A/G]AGCACTCCCACCCCC | 58513 |
rs181455784 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418641 | ACGGAACGTTTATGT[A/C]CCCCCAGATTCCTAT | 58513 |
rs181461730 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388428 | ACACCAAGAAAACTA[A/C]ACCCAGAAACTTCAA | 58513 |
rs181469357 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419334 | CATGGTGGCGCGCGC[C/T]TGTAATCCCAGCTGC | 58513 |
rs181469714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447709 | AGGCTGCAGTGAGCC[A/G]AGATCATACCACTGC | 58513 |
rs181614172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438903 | CACCACGATCCCCTC[A/G]GCCTCGTTGAATGGA | 58513 |
rs181616125 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401270 | AGCAGCCCAGGGGAC[A/G]CGTGTGCTTCCCCAT | 58513 |
rs181622095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466089 | CACCTCTCAGGTCCA[A/G]GCAATTCTCCTGCCT | 58513 |
rs181725534 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362599 | TGCAATCATGGCTTA[C/T]TGCGGCCTTGGCCTC | 58513 |
rs181742142 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409932 | CACAGAGTGAGACTC[A/T]GTCTCAAAAAAAAAA | 58513 |
rs181760699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388282 | TGGCCTCAAGTGATC[C/T]GCCCACCTCAGCCTC | 58513 |
rs181802642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377624 | ACACTTCAGAGACAC[A/G]CCCCACCCTCACCTG | 58513 |
rs181830990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400398 | TGAGATAAAGTCACA[C/T]TGCGTGAGCTTCACA | 58513 |
rs181833840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438131 | ACCGAGGCAGGTGGA[C/T]CACCTGAGGTCAGGA | 58513 |
rs181834770 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418964 | TCACAGCAGCCCAAT[A/G]GTCTAAAACACTCCT | 58513 |
rs181847036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456339 | AGAGGCAGCACTGAG[A/G]ATACAAAAGTGTGTA | 58513 |
rs181901336 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377890 | TGACCACCTCTGGCC[C/T]GGACCCTCGGTCAGC | 58513 |
rs181916294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396124 | AAAAAAAAATTAATT[A/G]AAGATCATTGAAGAA | 58513 |
rs181953258 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452252 | GGAGTTCTAAACCAG[C/T]CTGGCCAACATGGTG | 58513 |
rs181956679 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415733 | GCCTGTCACCTCCAC[A/G]TTGGGGAAACAAGGC | 58513 |
rs181957833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435971 | TGGCACTGTTTCCCA[C/T]GACAAAGTAGCTCTT | 58513 |
rs182087077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468089 | CTTCCTAGGTACAGC[A/G]GTCACAAAAGGGACC | 58513 |
rs182096711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405521 | CCTGGAAGCATACAG[C/T]GTGTGCAGAGGTATA | 58513 |
rs182100062 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372837 | CCCACCCGGGGCCTC[C/G]CTTTCCTCCAATGTC | 58513 |
rs182113518 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444284 | CCATCATTTTAAAAC[A/C]GACAAAGACATCATG | 58513 |
rs182122884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426063 | GACCGTATCAAGGCG[C/T]GCCCCACATGAGATG | 58513 |
rs182127651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461642 | AAAGAAAGAAAGAAA[G/T]AAAGAAAAGCCAGTT | 58513 |
rs182129865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397639 | TGTCCTATGAGGAAA[C/T]GAGTACTTATGCAGT | 58513 |
rs182154960 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358225 | GCAGGAAAGTTCCTG[A/G]TGCCTTCAGAGTCGA | 58513 |
rs182192245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404408 | TCTAGGAGTACAGGG[C/G]GGTGGCCAGGAAGTC | 58513 |
rs182209194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443745 | TAATAATGCCCGGAT[C/T]ATGGTCAGCGTCTCT | 58513 |
rs182366756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384388 | CCCCATTTCCAACTT[C/T]CCAGCAGTTTCTTCC | 58513 |
rs182414839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453633 | CAGGAGAATGGCGTG[A/C]ACCCGGGAGGCGGAT | 58513 |
rs182426976 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382504 | CACCAGTTGAAGAAC[C/T]GGTTCAAAACAGAAG | 58513 |
rs182457308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424202 | GCCCAGACAAGAGCA[C/T]TGCTGGCCTGGAGAT | 58513 |
rs182470598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460374 | CAGCAGATAAGTACA[A/C]ACCTGTAAAAACCCA | 58513 |
rs182487228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385935 | ATCACTGGTGCTATT[A/G]CTGAATTCCTACTGC | 58513 |
rs182507750 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427351 | ATGCCTGGGACCACA[A/G]GGTTTCAGTTCTGGA | 58513 |
rs182511062 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452518 | CCAGCTACTCGAGAA[A/G]CTAAGGCAGGAGGAT | 58513 |
rs182518063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407462 | AGGTGCACGCCACCA[C/T]GCCCAGTTGCGTGAT | 58513 |
rs182518941 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445659 | GCAGAGACCTCTTGG[C/T]CCCCAAAAGGAAGAT | 58513 |
rs182626709 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359358 | GCTGAGCCCCCGAAT[A/G]CCGTGAACATGGAGA | 58513 |
rs182639000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432816 | ATTATTATTATTATT[G/T]TTTTAAACAGAGTCT | 58513 |
rs182646728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470996 | CACAGAGAAATCGGG[A/G]CTGGAGCCAAGATTT | 58513 |
rs182652077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449719 | GGCCACAGCTTTATA[C/T]GTCACTGCTCCAAAC | 58513 |
rs182718183 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391814 | GCAGCCGGGCTGAGA[C/T]GCCTGCACTTACTCC | 58513 |
rs182722455 | snp | C/T | 0.00636936 | 0.0560724 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355223 | GGAAAACAATGTTTA[C/T]AGAGATTAAAGAAGC | 58513 |
rs182728569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365878 | GGGCTCGGCACACAG[C/T]GGGCTTCAGGAGGTC | 58513 |
rs182743193 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448987 | ATCAAATTAGAACAT[A/G]GGCAAGCCAGGCATG | 58513 |
rs182747369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411507 | TCTAACTCGATAGAG[C/T]GATGGTTAATCAACA | 58513 |
rs182750715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432279 | TCTCTATTAAAAATA[C/T]AAAAATTGGCTGGGC | 58513 |
rs182755013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379030 | TGTTCCTGGCCGGGC[A/G]CACTGGCTCACGCCT | 58513 |
rs182764320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402095 | GGTTCTGAAAGGATC[C/T]AGGCCTATCTTGGAC | 58513 |
rs182963037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436175 | AGGGAGCAAACCAAC[C/T]GTGTAAACATGGGAC | 58513 |
rs182966018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397033 | ATATACCTAACACTA[C/T]TGAACTGTACACTTA | 58513 |
rs183081614 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365947 | TCTCCAGGGACCTGG[C/G]GCCCTTTGGAGCAAC | 58513 |
rs183115688 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439211 | CTGTCCTCAGAAGCC[C/G]TTGCAGAGTGTAGAG | 58513 |
rs183125882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411970 | TCCCAAAGTGCTGGG[A/T]TTACAGGTGTGAGCC | 58513 |
rs183204857 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371647 | CTGCAGGCAGGAACC[A/G]CAACGCAGGGCCGCG | 58513 |
rs183253399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416245 | TCCATTTTCAGCCAA[A/G]TAAACAATCTCTTTC | 58513 |
rs183305418 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459031 | TACAAACCTGGGCAG[C/T]GTGGCCCGGTACAGA | 58513 |
rs183326103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370691 | AGAAAGTGCTCCAAA[C/T]GGCAATCTGCCTGCA | 58513 |
rs183328529 | snp | A/G | 5.13351e-05 | 0.00506606 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402510 | AAAGACATCATCAGC[A/G]TTAAGCAGGGTCAGG | 58513 |
rs183336674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421069 | AGCAAATGGCCTGGG[A/T]GCACTTAAGACGGAC | 58513 |
rs183344233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380112 | TGGTTACACAGATGC[G/T]GCCGTCTAAGGCTCC | 58513 |
rs183350537 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439996 | TCTTGTGAATCCAGA[A/G]GGCAGAGGCTGCAGT | 58513 |
rs183351307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420413 | GGACACTGTGTTTTG[C/T]TGGTTTCTAAAAGGG | 58513 |
rs183364876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458155 | TCCCTGCCAAGGACG[A/C]CAAGATCCCCTGCAC | 58513 |
rs183383576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392685 | ATATTTAATGAAACT[C/T]ATCTTATTACATAGT | 58513 |
rs183435874 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464430 | CACTGGCCACTCTCT[C/T]GGCAAGCAGACATCC | 58513 |
rs183499458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376016 | GATGACACAGGGGCT[A/G]CAAAGTGAGGCCAGT | 58513 |
rs183507317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400137 | AGGTCAGGAGTTCAA[A/G]ACCAGCCTGGGCAAC | 58513 |
rs183509051 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446218 | TGGAGAAACCCAGCA[A/G]AACCACCTCGGAGGA | 58513 |
rs183514420 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427765 | TGGCTGTGATGGAGT[A/G]CACCTGTAATTCCAG | 58513 |
rs183530124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418816 | TGAGGACACGGCAAG[C/G]AGGTGGCCGTCTACA | 58513 |
rs183535583 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470251 | AATTAGCCGGGTGTG[A/G]TAGCACGTGCCTGTA | 58513 |
rs183545749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440703 | CAAGTGTTTAAAAGA[C/T]CTTTATTTCAAAATG | 58513 |
rs183622956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423738 | TCTAATGAGAAATGG[A/G]CTTGCTGCCTTTTAA | 58513 |
rs183633492 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442592 | TTGTTCTCTGGCTCC[A/G]GAATCAGAAAAGAAG | 58513 |
rs183636540 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404264 | CGGGATCTGTGAGGA[C/G]CCTCAGAGACACCTG | 58513 |
rs183645945 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460289 | TCTCTAAAAATAAAA[A/G]AAGAACAGTGTTTCA | 58513 |
rs183802211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390163 | AAAGATCCAGGTAAG[C/T]TGAAAGTAAATGGTT | 58513 |
rs183802436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356428 | GGGATTCTCTTGCCT[C/T]AGCCCCCTGAGTAGC | 58513 |
rs183818439 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431433 | CTCAGCTTCCCGAGT[A/C/T]GCTGGGACTACATGA | 58513 |
rs183960872 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360338 | TGTTTCTGGCTTTTA[C/T]TAACAATGTCACCAT | 58513 |
rs183967582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406836 | GCCGTGTACTGAATG[C/T]CTGTTGTTGAAATTC | 58513 |
rs183973381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359833 | GCACCACTGCATTCT[A/G]GCCTGGGCAACAGAG | 58513 |
rs183993531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411449 | TGTTCAGGGCTAGAT[A/G]TTTTTATGGGCCTAC | 58513 |
rs184005087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364945 | GCACCCTGCCCAGAC[G/T]GCTTGAGGGCTTCTC | 58513 |
rs184022516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444651 | ACAGACTCCAGAGGC[C/T]CTCACTTCAGATGAC | 58513 |
rs184023243 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448862 | AAAAAGGTGAAAAGG[A/C]AAGCTACAGACTAGA | 58513 |
rs184087399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381598 | GCACATGGACCACAC[A/G]ACAATGATCACACCA | 58513 |
rs184102645 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357594 | CTGGGCAAGGTGCAG[A/G]AGCAGATAAATGCAA | 58513 |
rs184113970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403990 | GATGAAATGGGACTC[C/T]GAGAAAGAACTCTTA | 58513 |
rs184120367 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422972 | CGGGGAAAAAAAAAG[C/G/T]GGGGGGGGATTTCTC | 58513 |
rs184121858 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384866 | GGCAATGACTTCACC[A/G]TCTGAGACCTGATGG | 58513 |
rs184139470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386325 | CGTCGATGTACAACA[G/T]CCAGTGCTGAGCCAG | 58513 |
rs184158117 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426728 | TAGATCCCAGGAAAC[A/G]AAAGACAAAAGACAA | 58513 |
rs184164790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462952 | ATCCCACCGCTGTGG[A/G]TGCCACCTGACTTCC | 58513 |
rs184200785 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455766 | CCCGGGGACTTGTCA[A/G]TCACCGGCTGTTGTG | 58513 |
rs184278306 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360734 | GGCTGGGCAACACAG[C/T]GAGACCCTGTCACTA | 58513 |
rs184314193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407978 | GAAGTTTGGGGGTGA[C/T]AACACAGAATAACTG | 58513 |
rs184322228 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450982 | TGAGACAAGAGTCTC[A/G]CTCTGTTGCCCAGGC | 58513 |
rs184355253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438005 | AAAACCCCTTGGAGC[C/G]TTGGGCTGAACTGGA | 58513 |
rs184373233 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473003 | AAACAAAAAGAACCC[A/G]CTTGTAACTGTTGCT | 58513 |
rs184395500 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414320 | ATTCTTCCCCTAGAG[A/C]CTCCAACAAGAGCCC | 58513 |
rs184405479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367695 | AGGTTCTGACTTTTC[C/T]ATCTTGCTTTGCAGG | 58513 |
rs184414374 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450572 | TGCAACCTCCGCCTC[C/T]CAGGTTCAAGTGATT | 58513 |
rs184424589 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434236 | CACAGGAGCGCTGAT[C/G]AAAGCCCCTGATGGC | 58513 |
rs184428110 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473681 | GCAGGGGAGGTGGCT[A/G]GGCATAGTGGCTCAC | 58513 |
rs184480432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450188 | GGAGTTCAAGGCTGC[A/T]GTGAGCTATGATCGT | 58513 |
rs184735895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399391 | CAGGATGAATGACAC[A/G]GCCCTTGGCAGAGAT | 58513 |
rs184872589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366548 | CCTGGTTTTGCTCTG[C/T]TGCCGAAACCGTTGT | 58513 |
rs184883716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374604 | ATGGGAGGTGATAAC[C/T]GAGGGAAAGTTCAAA | 58513 |
rs184911658 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414719 | TTGGTTTTGTTTTTT[G/T]TTTTTTTTGAGACAG | 58513 |
rs184919733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441299 | AACACAGTGAAACCC[C/T]GTCCCTACTAAAAAT | 58513 |
rs185013770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398308 | ATAGCTGGAGCCTCC[A/G]ACCACAGGGTTTTCC | 58513 |
rs185020133 | snp | A/G | 0.018099 | 0.0933912 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362001 | TGGAAAGTTTAGGAG[A/G]AAAAAAAAAGGAGAA | 58513 |
rs185021049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380769 | TTGCACAGACATGGC[C/T]GTTTAGGCCTCTGGA | 58513 |
rs185024222 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373628 | GACCGCTCTTGCCCA[C/T]AACCAGAGGCCTCCT | 58513 |
rs185037294 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434867 | TGTACCAGAAAGACA[A/G]AAGTGTGAGCAGATG | 58513 |
rs185040394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422377 | CCACAGTTCACGGCA[C/T]CTGTGTCCTGAACTC | 58513 |
rs185041907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437187 | AAATGAATTAAAAAC[A/G]GATGTCCAAACAAAT | 58513 |
rs185044105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459424 | TCACGCTGTGCCCTC[C/T]TAGAAGCAGGCCTTC | 58513 |
rs185060543 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454363 | CACACGGTATCCTAT[C/T]GCCCCGCTACTGGAA | 58513 |
rs185088248 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395282 | TCTAGTTGAAGAACC[A/C]CTCTAAATTCGACAT | 58513 |
rs185098291 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370239 | ATATTTTGCAGTTAG[A/C]AGTGGCAGGCAAGGG | 58513 |
rs185125596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357060 | AAACAATCCCAGAAC[A/G]ATCCAGGACCCAAGG | 58513 |
rs185173151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437367 | CCCTGAAAACACGAT[A/G]CTGAGAGAGAGGCCA | 58513 |
rs185233079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466644 | GCGGTGCCTCCTGCC[C/T]GTAATCCCAGCACTT | 58513 |
rs185239823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448085 | AAAGTCTTATGCCTC[C/G]TACAAAATGTAACTC | 58513 |
rs185297540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418225 | GGCAGGGCGTGGTGG[C/T]AAGCCCCAGCTCCTT | 58513 |
rs185300142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454854 | ACAGCTCTGGGCCAG[A/G]CATGGTGGCTCACAC | 58513 |
rs185363566 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444315 | GAAAAGACATAGGAG[G/T]TAAGTGTGTATAGCA | 58513 |
rs185373367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426220 | AGGCCCATGTGGGGC[A/G]GGTGTGACCTCCGTG | 58513 |
rs185544436 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433273 | TCTGGGATTACAGGC[A/G]AACACCACCACACCT | 58513 |
rs185546514 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393477 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 58513 |
rs185550575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358091 | AACGACCAAGTAACC[A/G]GCCTGCTGGGTCTGA | 58513 |
rs185665261 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413788 | CTGCACCTCGCTGGT[C/T]TTCTGTCTGATTGCC | 58513 |
rs185669339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382219 | CCTGGCACTGCCTCC[A/G]CAGTGAATCAGATCA | 58513 |
rs185687374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363044 | GTGCATCCTGCCAAT[A/G]TACCAGAACATTCCA | 58513 |
rs185701693 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408885 | AACTCATCCTTGACA[A/C]GGATGCTAGGGCCAT | 58513 |
rs185710283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447219 | AAGGCATCAGGGAAA[C/T]GCTGGGGTATGTCTA | 58513 |
rs185744328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371011 | TTGTAGAATTTCACA[C/T]GTACCCACCGGATTA | 58513 |
rs185782610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396226 | GACTAACAGGAGGAA[C/T]TGGGTGTGGGATATA | 58513 |
rs185789367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436072 | TGCTTGATGACAGAG[A/G]TGACTGCATGACTCC | 58513 |
rs185791439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415961 | CCAGTTTGGATAACA[C/T]GGCCCCCAGGAGCTG | 58513 |
rs185803873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452370 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGTTTG | 58513 |
rs185827310 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429178 | GCTGGGCAGGGCTGC[A/G]AGCTCATGTCTGAGC | 58513 |
rs185829772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387324 | CAAAAATTGGCCAGG[C/T]GGGCAAGGCACAGTA | 58513 |
rs185830241 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358825 | CTCCTTCAATAATTC[C/G]AAGCACGGCCTAGCT | 58513 |
rs185833330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388893 | GGCTGGAAGGCAGTG[C/G]AAAAACACACTAAAC | 58513 |
rs185848452 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405382 | GGAGCCCGGTGGGAT[A/G]TGTGAGTGTGGGAGG | 58513 |
rs185857103 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465312 | TGAGCCTCTGCTGTG[A/G]GCCGGGCCTGGACAA | 58513 |
rs185860524 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425579 | ATATGCATCCCTTCA[A/C/T]CACTCAGGGAGGCCA | 58513 |
rs185861946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430916 | GGATGCGGAGGGACA[C/T]GGGTGCATAGATGCA | 58513 |
rs185862626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384176 | CCCTGCAGCCCCCCG[A/G]AGACAGAGCCCATCT | 58513 |
rs185877335 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444183 | AGTCAAAAAAAAAAA[A/G]AAGAGGAAAAGAAAG | 58513 |
rs185902843 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458052 | AATGTCCCTGCCATC[C/T]ACTACTCCCTAACAG | 58513 |
rs185973002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364669 | AGTTGCCCCGTTCCC[C/T]CTCCTAAGGGACGGG | 58513 |
rs185987478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405653 | GGAACGGGATGGCGC[C/T]GTGTGCTTTGCCTTA | 58513 |
rs186004979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435731 | AGAAATGTTCACAAC[A/G]GAAACAAACACTTGG | 58513 |
rs186097628 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409976 | AAATCAGCTATAAAA[A/G]GAACCCAATTAACCA | 58513 |
rs186112716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388322 | TGGGATTATAGGAAT[A/G]AGCCACTGAACCGGC | 58513 |
rs186118350 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447883 | TAAGACAGTGGAGTA[C/T]TGGCAGGGGGCGGGC | 58513 |
rs186126810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415324 | TCAGTCACCCATTCA[A/G]AGTGGTTTGTTATAG | 58513 |
rs186126901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451250 | GCCACCGCGCCCGCC[C/T]AGACTCTCCAACAAC | 58513 |
rs186130135 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430179 | GGGGCACCTCTTCTA[C/G]AAAGTCTTCCCCAGC | 58513 |
rs186133150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384536 | GTCTGGAGAAGCCCT[A/C]CAGCTGTCTGGGACC | 58513 |
rs186140984 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466193 | GGGTTTCAGCATGTT[A/G]GCCAGGCTGGTCTTG | 58513 |
rs186420365 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390489 | AGATTATCTGAACAC[C/T]ATGAGGAACCTCAAC | 58513 |
rs186426624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400462 | CATAGGAAGTTCCAG[A/C]TGTACCACTGTGGAT | 58513 |
rs186429822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438775 | GTCCTCCTGCCTTAG[C/T]TTCCTGAGTAGCTAG | 58513 |
rs186434512 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365481 | AACCCCACTGGCGCC[C/T]TGATCTTGGACTTTG | 58513 |
rs186440836 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456449 | ATCACATGAGGTCAG[C/G]AGTTCGAGACCAGCC | 58513 |
rs186501717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369096 | TTTTCCCCAACACAC[A/G]TCAACGTCTTCCTCT | 58513 |
rs186616622 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471680 | GGGCGGAGAGGACAC[G/T]CGCTGCGCACCTCCT | 58513 |
rs186639089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382684 | TGTTTTTATTCTCAA[A/G]TGCTCCCTGGAAACA | 58513 |
rs186643261 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424509 | CTTTCAAAACTCTTG[G/T]CAAGAGCTCTGCAGA | 58513 |
rs186648602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460777 | CATGCGCCTAGGCCA[A/G]TCGTGTCTGGGACCC | 58513 |
rs186676469 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355227 | AACAATGTTTACAGA[G/T]ATTAAAGAAGCTTCT | 58513 |
rs186698289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394418 | CAGCAATGAGGCGGC[A/G]GCACCCCTGGGCTTC | 58513 |
rs186708740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379511 | AACAGATTGCAGATG[C/T]GGGGGAAAAGGTCTA | 58513 |
rs186719562 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402174 | AGGCCTGGTGTGAAC[A/G]CGCAAAGTGGCAGCA | 58513 |
rs186729462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439726 | CAACAAACATGCAGA[C/T]ATGCACCATGAACCT | 58513 |
rs186793888 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438952 | CAGTGGCCTGACGTG[C/G]ACCCCACCTAGACAC | 58513 |
rs186800948 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401322 | TGGCTGCTGAGAAAA[A/G]AAACACATCAAGCAT | 58513 |
rs186829727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358261 | TCAAGGCCAGCTCAC[A/G]AATCCACTGTGGAGA | 58513 |
rs186841549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407608 | TGGGATTATAGGTGT[G/T]AGCCACCATGCCTGG | 58513 |
rs186841884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446151 | AAGGCTTTAAAACAC[C/T]GCAATTCACACAAGC | 58513 |
rs186844842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416998 | CACCTTCAGCTGCTG[A/G]GTCCTAAGCCCGCTC | 58513 |
rs186846270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427472 | TTCCTTTGAGTGTCA[C/T]GTTGATGCTCAAAAA | 58513 |
rs186856037 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464810 | AATTCACGGGTGGGC[A/G]TGGTGGCTCACGCCT | 58513 |
rs186857228 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372949 | TCCTGTCCTGGCCTC[A/C]CACATCAGCCATTTC | 58513 |
rs186864573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397736 | CAGGTTCATTTAAAC[A/G]AGAAGAAAAAATATT | 58513 |
rs186865512 | snp | A/G | 0.00122791 | 0.0247477 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404550 | GGGAAGCCCCTGCCT[A/G]TGCATAGGGCGCTGC | 58513 |
rs186876624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443918 | AAATACAGAAAATTA[C/G]TCAGGTGTGGTGGTG | 58513 |
rs186980701 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378539 | GCTTCCTGCCACCCA[A/C/T]GCCTGCACTGCTCAC | 58513 |
rs186997962 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419423 | AAGATTGCGCCAATG[A/C/T]GCTCCAGCCTGGGCA | 58513 |
rs187022768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457463 | AGGCTGTGGAGCACC[C/T]GCACCAAAGCAGTGC | 58513 |
rs187180986 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385966 | CAAAATTCCTTTCTG[A/G]AAAGATGCCAGCGCG | 58513 |
rs187191461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360608 | AAACATTAGCCTTGC[A/G]TGGTGTTGCACGCCT | 58513 |
rs187196642 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468448 | CCGCCTGGTTTCAAG[C/T]GATTCTTGTGCCTCA | 58513 |
rs187302338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360175 | TCTTCAAGCTGCCGT[C/T]CACCCCACTTACCTA | 58513 |
rs187348598 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377814 | CCTCAGGTGGAAGTG[C/T]ATCCTCACATGCCCG | 58513 |
rs187399969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365905 | GGTCCTGGTGAACCA[C/G]GTGCCACCTGTTACA | 58513 |
rs187404130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391856 | GAGCACCTACCAAAC[A/G]TGACTCTAAGGTCCC | 58513 |
rs187412959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411475 | CCTACTGGCGCCTAC[A/G]GGAGAAACAATCAGG | 58513 |
rs187414525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448910 | CACATATCCAACAAA[C/T]GACTACTATCTAAAA | 58513 |
rs187432314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357180 | GCAGCACTAGGTCTG[C/T]GTGACAACCTGGGGG | 58513 |
rs187433932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449529 | CTCATACACTGCTGA[C/T]GGGAAAGTTAAAAGG | 58513 |
rs187437117 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411605 | CCATCCTTCAGATTG[G/T]TATTAAAATTTGCAG | 58513 |
rs187438713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432485 | AGGCAGGAGAACGGC[A/G]TGAACCCAGGAGGCG | 58513 |
rs187442972 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470517 | CCCGCCCCCCACCCC[C/T]TGACTACATACTCTA | 58513 |
rs187456302 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398727 | CACAGGTGCAATCCC[A/G]CTACTGAGCAGCGTG | 58513 |
rs187483779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437335 | GAAACACTGATCCAT[C/T]CTACAACATGGATGA | 58513 |
rs187494719 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454369 | GTATCCTATCGCCCC[A/G]CTACTGGAACCTGGC | 58513 |
rs187549300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392991 | AGGCTGCAGTGAGCT[A/C]TAATTGCGCCACTGC | 58513 |
rs187552327 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433121 | AGCCTAAATTGAGGG[G/T]TTTTTTTGTTTTTGT | 58513 |
rs187631204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359582 | AAACAGAAAACAGGC[C/T]GGGCACAGGGGCTCA | 58513 |
rs187657057 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431644 | GCACAACAGGGGAAC[C/T]ATAGCTAACAATAAT | 58513 |
rs187666950 | snp | G/T | 0.00364153 | 0.0425148 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437107 | TTTCAAAAAAGGGAA[G/T]ACTTCACAAAGTTAA | 58513 |
rs187684311 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440294 | AAAAATTAGCCAGGC[A/C]TGATGGTTCTCGCCT | 58513 |
rs187700809 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421218 | ACAGCGGAAGCCTGT[A/G]ACAGGCTGGAGGGGG | 58513 |
rs187709565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458458 | GCCGCCCCGCCCCCA[C/T]CCCGCTTGCCCCATA | 58513 |
rs187777781 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366118 | GGAAACAGTTAAGTG[C/T]TTCCAGGGGAGAAGC | 58513 |
rs187792655 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452599 | CTGAATGGCTACTGC[A/G]CTCCGGCCTGCACAA | 58513 |
rs187817209 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412647 | AATATATATATATAT[A/T]TTTTTAAAAACTTCT | 58513 |
rs187825294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449800 | GTCCAAGCACACCAT[A/G]GAATACTACTCAGCA | 58513 |
rs187944805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453970 | AGGTTTAAGTGTGAC[A/T]AATGAGGAGAGCTTG | 58513 |
rs188083604 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381701 | CATGAGGGGCAGTGT[C/T]GGCCTGCAGCTTAGC | 58513 |
rs188103700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357650 | GCAGTGAGGGGGATG[C/T]GGGGCCCTGGAGGCC | 58513 |
rs188120194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403997 | TGGGACTCCGAGAAA[G/T]AACTCTTAGCCCCCA | 58513 |
rs188122141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442053 | AGTGGCACCCGCCAC[A/G]CTAACTATCCGCTGA | 58513 |
rs188126585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423299 | AGGCCAGGCACAGTG[C/T]TCATGCCTGTAATCT | 58513 |
rs188140494 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372578 | CTCACAGGGAGAAAA[C/G]GGCCCAATTAATGAC | 58513 |
rs188141366 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460053 | ATTAAGGCAGGAGGA[G/T]CCCTTAAGGTCAGGA | 58513 |
rs188152278 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416390 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 58513 |
rs188234557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376664 | GACTGGACCAAGCAG[C/T]GACTCCTGCCACCCT | 58513 |
rs188238686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400207 | CTGGGCATGGTGGCA[C/T]GTGCCTGTAATCTCT | 58513 |
rs188251748 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465011 | ATGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 58513 |
rs188261111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446227 | CCAGCAGAACCACCT[C/T]GGAGGAGAAACTGTC | 58513 |
rs188271560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418846 | AAACTAGGCAGTGAG[C/G]CCTCACCAGACACTG | 58513 |
rs188273387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438120 | CACTTTGGGAGACCG[A/G]GGCAGGTGGATCACC | 58513 |
rs188285349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455803 | GGTATCCTCCTCATC[A/G]CCCTCCTTCCACTGG | 58513 |
rs188307497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426831 | GTAATATCCTGGGAT[A/T]AGATAATAATAGACA | 58513 |
rs188337958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463128 | CCAGCCCCAGAGCTG[G/T]TCTTCTTTTTGACTG | 58513 |
rs188453940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436226 | TTTGAGAGCAAGAGT[G/T]TTATTCATGTCAGGA | 58513 |
rs188455423 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397385 | GTGAGCCACCGCGCC[C/G]GGCTGTTTGTCTATT | 58513 |
rs188472919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441237 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGATTCAC | 58513 |
rs188510911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410063 | CATTTGAACCCAGGA[A/G]GCGGAGGCTGCAGTG | 58513 |
rs188521417 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363440 | CTCATCCGGTAGAAC[A/G]AGCCCACACAGGCCA | 58513 |
rs188529441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388418 | AACAGTATAAACACC[A/G]AGAAAACTACACCCA | 58513 |
rs188531723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447930 | AGAACAGAATGTAGA[A/C]TCTGAGAAACAGACA | 58513 |
rs188539822 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430502 | AGACACAGTCCTTAA[A/C]AGGAGGGCTGCAAGT | 58513 |
rs188543908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466451 | GAATGCACTACACAT[C/T]GGGCTCATTTCTTTA | 58513 |
rs188573735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407162 | GGACTAAGACACACA[C/T]GCCATGTCAGCGTCT | 58513 |
rs188601036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374021 | GATCTGCAGTTGCTC[C/T]GGACTTAAAATGCTG | 58513 |
rs188605102 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445159 | CTTCCCAGGCGCTAA[C/T]GAGCAACAAGATCCG | 58513 |
rs188608255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450364 | GTTCTATTGCTTCTC[A/G]GTTCCTCTCCAGGGC | 58513 |
rs188712198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380798 | GAGTCTAGTCAGAGA[C/T]GTGGCCACCTGTGTC | 58513 |
rs188748183 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459214 | CCCTATGCTTGGGGC[C/T]GCTGCCTGCTGCAGG | 58513 |
rs188752259 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422660 | CATTCCTCTCAGTTA[C/T]GAAAGGATTTCTTAG | 58513 |
rs188870372 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433384 | TTATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 58513 |
rs188903992 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473232 | TCAAACAGAGGATAT[G/T]GAATACAGGGGATTG | 58513 |
rs188968401 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380138 | GCTCCGGCATCTAGT[C/T]GCACAGACGCAGCCA | 58513 |
rs189008439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362249 | CAGCTAAAACTTGAG[A/T]TGTCCTAGAATAGTT | 58513 |
rs189033863 | snp | G/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356357 | TCGCTCTGTCGCCAG[G/T]CTGGAGTGCAATGGC | 58513 |
rs189039659 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387690 | AGAATGGCTTGAACC[C/G]AGGAGGTGGAGGTTG | 58513 |
rs189128805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394655 | TCTGGACAGACTCCT[A/G]AAATTATCCAGACCT | 58513 |
rs189149383 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434873 | AGAAAGACAAAAGTG[G/T]GAGCAGATGTTAGTG | 58513 |
rs189154316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414511 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCCT | 58513 |
rs189169685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443322 | ATAAAACCAGGGGGA[C/T]GTAGACTCCTTCCAG | 58513 |
rs189177091 | snp | C/G | 0.000170282 | 0.00922563 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434518 | AAATAGCCCGAGTAA[C/G]TAGGAGAGCACACCT | 58513 |
rs189185025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460337 | AGCTGTCATTTTCTT[A/T]AAAAAAATACAATTT | 58513 |
rs189191321 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450703 | GGCCAGGATGGTCTC[A/G]CCCTCCTGACCTCAG | 58513 |
rs189216697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356674 | CTGCCATTTAGTCAA[A/G]TTTTTATCCGTGGGG | 58513 |
rs189223396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360889 | CCCAGGAGTCGAAGC[A/C]TCTATAAATAACACA | 58513 |
rs189240075 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402892 | ACTGCGCAAAGCAAC[A/G]TATCTTTGCTCCTGA | 58513 |
rs189267455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408250 | AGAAGACAAAAATAA[C/T]CCCAACAGTCCACGG | 58513 |
rs189274426 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414247 | AGGAAAAAGAGACCT[C/T]GGACCCCCAGCCGCA | 58513 |
rs189291004 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393486 | AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT | 58513 |
rs189392061 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374674 | GGGTGGCGGTTTCCA[A/T]GAAACACTGAAAATG | 58513 |
rs189412142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418627 | TTTCCTTGTTATGAA[C/T]GGAACGTTTATGTCC | 58513 |
rs189414080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455475 | CTGCAGCAGGCTTCC[A/T]GCCTCGATGCACTGC | 58513 |
rs189429580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369979 | TTTGTTCCTCCCTAC[A/G]GAGTGTGCCAATGTC | 58513 |
rs189443838 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414909 | CCGAGGTCTCAATAT[A/G]TGGCCCAGGCTGGTC | 58513 |
rs189451352 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451202 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 58513 |
rs189547250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386980 | CATATAAAGAACTGG[A/G]AAAATGTGACCACCT | 58513 |
rs189551413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428868 | ACTCACTGGGCTCAG[A/G]AGACGGCAGTCAATA | 58513 |
rs189634144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367261 | GGGACCACAGCAGAC[A/G]GCAGTGAATAAAGAC | 58513 |
rs189663225 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399780 | TCCCACCTCAGCCTC[C/T]CAAAGGACTGGGATT | 58513 |
rs189679871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437414 | TTAGAGAATTCCATT[C/G]ATAGGAAATGTCCAG | 58513 |
rs189805669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358985 | GGAAGAGGTTTCCCG[A/G]GAACAGCCACACACG | 58513 |
rs189826493 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405505 | CTTCCAAGAAAAGCA[C/T]CCTGGAAGCATACAG | 58513 |
rs189834782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425866 | CATCCATGAGGCAGG[A/C]CACAGCCATAGAAAT | 58513 |
rs189842471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384311 | TCACTCAAACAGGGA[A/G]ACATACAACTCACAA | 58513 |
rs189951337 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429380 | TGGATGGGCACACTG[C/T]CTGCCAGGCCAACGC | 58513 |
rs189958917 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356323 | TTTCTTTTTCTTTTT[C/T]TTTTTTTGAGATGGA | 58513 |
rs189974243 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402251 | ATGAACAGATCTGGC[A/G]GGTGGGATGTTCTGC | 58513 |
rs189982111 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420665 | CAATTCTTTCCTTTT[C/G]ATAGCTCCCAAGTGA | 58513 |
rs189982614 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465436 | CACCTGTAATCTCAG[C/T]GCTTTGGAGGCAGAG | 58513 |
rs189988452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379548 | CGTCCAGCAGACAGT[C/T]TTAGAGGTATGGCTG | 58513 |
rs190004532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439887 | CTGAGTATTCCTCAT[C/T]CCAAATGCTTGGTAT | 58513 |
rs190009894 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470941 | CATTTTCCAAAGGAA[A/G]CAACTGATGGGTGGA | 58513 |
rs190020058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449671 | CGGGAGAAATGAAGA[C/G]TCATGTTCATACCAC | 58513 |
rs190021089 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458082 | GAGCACACTGCCCAG[C/G]ACTCGGTTGGGATGG | 58513 |
rs190070937 | snp | A/T | 0.0115144 | 0.0749975 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355139 | AAAAAAATTTTTTTT[A/T]AAAGTAAAAACTTAA | 58513 |
rs190076313 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367834 | TGCAAACCATAAAAA[C/T]GGTGAATGCTATAAA | 58513 |
rs190112491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405062 | TGCAGCTGTGGCTGC[A/G]GAGGGGAACATCACC | 58513 |
rs190120771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444059 | ACGGTGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 58513 |
rs190191783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408919 | ACGGGGGAAAGAAGA[A/G]GCTCTTCAACAAATG | 58513 |
rs190199256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382332 | CAACTCTTTCCTACT[C/T]GGGCAGCGGCTTCAA | 58513 |
rs190213993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424154 | GCTTCACTCAAACCT[A/G]GCATGAGGGCAAAAT | 58513 |
rs190224332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447708 | GAGGCTGCAGTGAGC[C/T]GAGATCATACCACTG | 58513 |
rs190249356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444274 | GATTTAGGAGCCATC[A/G]TTTTAAAACAGACAA | 58513 |
rs190265722 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461524 | CTACTCGGAGGGCTG[A/C]GGCTGGAAAATCACT | 58513 |
rs190356124 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424812 | ATTACAGGTGCGCAC[C/T]ACCACACCCAGCTAA | 58513 |
rs190384880 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461122 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 58513 |
rs190437653 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358147 | CCCCACTGAGCCCCC[A/G]TGTCACAGTGTCACT | 58513 |
rs190475025 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419329 | CCGGGCATGGTGGCG[C/T]GCGCCTGTAATCCCA | 58513 |
rs190480618 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404357 | TCAGGGCACAAGTTC[A/G]CAGGGACCAAGGCCA | 58513 |
rs190484995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390812 | AATGGCAATGAAGAG[A/G]TAAAGTATTCAAATA | 58513 |
rs190491840 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438876 | GTTGGTCAGAAACTC[A/C]TATCTGTGGTTCACC | 58513 |
rs190495766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365614 | ACAGTGTGACAGTGT[C/T]CTGCACCCCAGCCTG | 58513 |
rs190638573 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436163 | ACCTCTCCAAGAAGG[C/G]AGCAAACCAACCGTG | 58513 |
rs190644555 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416214 | ATCCATCCTCCCTGG[C/G]AAAGTCAAAGCCCTT | 58513 |
rs190657560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452408 | CTGAGATTATGCTAC[C/T]GCACTCCAGCCTGGG | 58513 |
rs190721110 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358546 | CGAGACACCGTAGGG[A/G]CATGACACCACCCTA | 58513 |
rs190725712 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370664 | TTTCAAACTCAGTGG[G/T]CTTTACAGAACAGAA | 58513 |
rs190729692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395590 | AAAAAGAATGATTTA[A/G]CCAGGAGTTCGAGGC | 58513 |
rs190748348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382702 | CTCCCTGGAAACATA[C/T]TTTGGGGAATCTGTT | 58513 |
rs190763237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415503 | CACAGTAAGTGATCA[C/T]TGGAATATTCATTTC | 58513 |
rs190767361 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435969 | CTTGGCACTGTTTCC[C/T]ATGACAAAGTAGCTC | 58513 |
rs190889208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411235 | AGGAAATGTGCCCCA[C/T]TGTGGCTGGGTACAA | 58513 |
rs190899713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456588 | CTTGAACCCAGGAGG[C/G]TAGAGGTTGCAGTGA | 58513 |
rs190920719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462466 | AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT | 58513 |
rs190923943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448506 | TTGCACCATTGCACT[C/T]CAGCCTGGGCAATAA | 58513 |
rs191012263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372725 | GACCACATACAGCAC[A/G]TCACCGTGCAAGGCG | 58513 |
rs191036355 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419867 | TGCCTCTCCACTCCC[A/G]CCCCTTCTCTGCTCC | 58513 |
rs191046561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378699 | CCTCACTTGGAGCGC[C/T]GGTGAGGCACAGGGG | 58513 |
rs191056151 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457866 | AGTCACCCAAGACTG[G/T]GGGGGAGGGGGGAAC | 58513 |
rs191094577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460257 | CCACTGCACTCCAAC[A/C]TGGGCGACAGAGCCT | 58513 |
rs191131064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389868 | TGATATTTCCTAAAG[C/T]AACCTCTAAACAATC | 58513 |
rs191156012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431327 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 58513 |
rs191167909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466990 | CAAAGCAGGTCAAGC[A/G]AGTCCACAGTACCAT | 58513 |
rs191194223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436707 | TGTCCAGGTAGGCAA[C/T]TCCCAATTCCAGTGA | 58513 |
rs191206985 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397494 | CTGTAAAGAGCCACT[A/C]AACAACAGCAGCACA | 58513 |
rs191294719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401595 | ACATGTCCCCAGGTT[C/T]GAGGCTGCAGGGGCA | 58513 |
rs191423538 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416680 | CCAGCATGGTGGTGC[A/G]TCCTAGCTACTCGGG | 58513 |
rs191448933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453146 | GCTCTGTCACCCAGG[C/T]TAGAGTACAGTGGTG | 58513 |
rs191470262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442551 | CCTGGAGAGCTCAGA[A/G]GGAAAGGACACTCTA | 58513 |
rs191478412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423700 | CTCAAGTCTGGTGGA[C/T]GTAAAGATGCCAATA | 58513 |
rs191538672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392665 | CAAATTGCACACAAC[C/T]GTGCATATTTAATGA | 58513 |
rs191553602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381161 | AGGCAGGAGACACTC[A/G]CTCTGTGCTGATCTT | 58513 |
rs191566064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357457 | GCTGGGATTTCCCCG[G/T]GGAGGCTCCTTGGGC | 58513 |
rs191571691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432525 | GTGAGCAGAGATTGC[A/G]CCACTGTACTCCAGC | 58513 |
rs191572557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400737 | ACATTCCCAAAGTAA[C/T]TGTGTCTCAGGTAAC | 58513 |
rs191573474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411720 | TTCATTTATTTTTGA[A/G]GCAGGGTCTCACTCT | 58513 |
rs191693083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371300 | CACCCCCGGCAGGGA[C/G]GTCAAGAACTCACGG | 58513 |
rs191694456 | snp | A/G | 0.000115015 | 0.00758251 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386242 | TCGAGCTAAATGAAA[A/G]GAGAGAGGAAAGAGT | 58513 |
rs191719246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446167 | GCAATTCACACAAGC[A/G]CCTGTAACTGTAACC | 58513 |
rs191726088 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407679 | GATATATAAAATCAA[C/T]AAAGCTGAAATACAC | 58513 |
rs191732624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427533 | ACTTTCAGATTAAGG[A/T]TACTCAACCTATACT | 58513 |
rs191738505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464854 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACAAGG | 58513 |
rs191799684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377888 | TCTGACCACCTCTGG[C/T]CCGGACCCTCGGTCA | 58513 |
rs191847286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451397 | ATGGTCTTGTTATCA[C/G]ATAATACCAATACCA | 58513 |
rs191855280 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384593 | TGTGGTGAGGGCCGG[A/G]CACCAACGGGTCCAG | 58513 |
rs191865438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426405 | TTTGGAGGCCGAGAC[G/T]GGCAGATCACCTGAG | 58513 |
rs191965386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431959 | TGGATACAAAATACA[A/G]TAGTCGTGGGACGTG | 58513 |
rs191993233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468782 | TTTAGGAGGCTGAGA[C/T]AGAAGGATTGCTTGA | 58513 |
rs192020686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396290 | TTTCTGAAACAGGGT[C/T]TCACTCTGTTGTCCA | 58513 |
rs192144071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406694 | TGCCCAGAGAAGTTC[C/T]CTCCTTTACCTCCTC | 58513 |
rs192150812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359613 | TGCCTGTAATCCCAA[C/G]ACTTTGGGAGCCTGA | 58513 |
rs192185220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444570 | GGCAGGCTGTTTGTC[A/T]TCTGTCAGTAAAGGT | 58513 |
rs192230234 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385678 | CTGCTACCCGCCCCA[C/G]GCAAGCTGCAGGACC | 58513 |
rs192247787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360214 | CTACCCAAGACAGAG[C/T]ACCTGAGTCATGTGT | 58513 |
rs192261331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407291 | TCTCCCTTCCCTTTC[C/T]TCTCCCCACTCCCCA | 58513 |
rs192313235 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448937 | AAAATATATACTAGA[C/G]AGCTCTCAAATTCAA | 58513 |
rs192329504 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437360 | GGATGAACCCTGAAA[A/G]CACGATGCTGAGAGA | 58513 |
rs192343267 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454385 | CTACTGGAACCTGGC[A/G]GGACAGGGCCATGCT | 58513 |
rs192423270 | snp | A/T | 0.00200046 | 0.0315631 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417528 | AACATCTGGATGTGG[A/T]GGGAAGGGCCGTTTC | 58513 |
rs192434114 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373203 | GTCTGTCTATCTCCA[C/T]CAGCTCAAGGCTCGA | 58513 |
rs192438308 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398030 | AAGCCGGGGCGTCCA[C/T]AAAAATAGGGACAAT | 58513 |
rs192445951 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437186 | CAAATGAATTAAAAA[C/T]GGATGTCCAAACAAA | 58513 |
rs192455478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366212 | TGATTTCTCGAAGCC[A/G]TTCCTGCAGGGAGTG | 58513 |
rs192459822 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454105 | AAGTGATGCAGGAGT[C/G]GGGGAAGGGTAAGAG | 58513 |
rs192472375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413179 | TGGCCAAGCTCTCCA[G/T]TGTCCCCGTGTGCAG | 58513 |
rs192508043 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449832 | TGAAAAGGAATGAAC[A/G]GCTGACACATATGCA | 58513 |
rs192544341 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414260 | CTCGGACCCCCAGCC[A/G]CAGGGAAATGGATTC | 58513 |
rs192552059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367356 | GGGCAAGGGATACAA[A/G]ACTGAAGAAAACACA | 58513 |
rs192552228 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458853 | CTCCTTGTCTTGGCA[C/G]AAGATGCAGTCATGC | 58513 |
rs192554938 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393515 | TTAGCCGGGCGTGGT[A/G]GCGGGCGCCTGTAGT | 58513 |
rs192558257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450383 | CCTCTCCAGGGCAGG[A/G]AACGCATGCCTTACC | 58513 |
rs192566140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433918 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 58513 |
rs192640028 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459280 | CAAATGAAATAAGTC[C/T]CTCCTGCCTCCACAC | 58513 |
rs192642193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422786 | ACATGGTGAAACCCC[C/T]TCTCTACTAAAAACA | 58513 |
rs192708598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360652 | CTCAGGAGGCCAAGA[A/C]AGGAGGATCGCTTGA | 58513 |
rs192798082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433268 | AAGTGTCTGGGATTA[C/T]AGGCGAACACCACCA | 58513 |
rs192799116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392998 | AGTGAGCTATAATTG[C/T]GCCACTGCACTCCAG | 58513 |
rs192812348 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472148 | CAGCCTGGAGGGGCT[A/G]GGCCTGAGGCATCTG | 58513 |
rs192841564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365939 | TCCACGGGTCTCCAG[A/G]GACCTGGGGCCCTTT | 58513 |
rs192855827 | snp | A/G | 1.73225e-05 | 0.00294295 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403928 | CGTTTTCAGTGATGA[A/G]ATCTGAAATGAGATG | 58513 |
rs192873956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441245 | GGAGGCCAAGGTGGG[C/T]GATTCACCTGAGGTC | 58513 |
rs192983154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417885 | GTGTGCCACCAGTGC[C/T]ACCTGGTGGCAGGCG | 58513 |
rs192987877 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445432 | ATCTAATTACACATA[C/T]GTCAGGTTTTGCATA | 58513 |
rs192988993 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374491 | TCCCGTTATCAAACG[C/T]TCTACTTTTAACAAG | 58513 |
rs193059413 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387302 | AACCCTGTCTCTACT[A/T]AAAATACAAAAATTG | 58513 |
rs193061510 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429109 | GGTGTTGCCCTAAAC[A/T]CCCACACTCCCTATG | 58513 |
rs193065849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465291 | CAGCTTGGACCACCC[A/G]TGACCTGAGCCTCTG | 58513 |
rs193098124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403318 | TGCTCCAGGGTGGCG[A/C]CTCCTGAACACACCA | 58513 |
rs193101529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon, missense | EPS15L1 | GRCh38.p7 | 19:16356945 | AATGTCTCTCTGCGA[C/T]GCACTGCCTCTGACC | 58513 |
rs193103749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440519 | TCACTGGGGAGAGCT[G/T]GCAAAAGATACACAG | 58513 |
rs193115240 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473292 | CCCAGCAATCCAGTT[C/G]AGACAGGTAGATTGA | 58513 |
rs193192722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426848 | GATAATAATAGACAC[A/G]CTCATACAGAATATA | 58513 |
rs193193265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398739 | CCCACTACTGAGCAG[C/T]GTGGGAGTTTTGACC | 58513 |
rs193200869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464362 | ACCAGCGGTAAAACC[C/G]AGTCCAGCGCGAAGG | 58513 |
rs193223108 | snp | A/C | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361115 | ACAAAGCCAGGCTTT[A/C]GAAATCCCGAGATTT | 58513 |
rs193234264 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408814 | TGGCATGAGGAGAGG[C/G]AGATAGGTCAATGGG | 58513 |
rs193237703 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446640 | AAGCACCCAGGATAG[A/G]TGGTCCTGGAGTCAG | 58513 |
rs193259548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380190 | CACACAGACGTGGCC[A/G]TGTAAGGCTCCAGCA | 58513 |
rs193263277 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422073 | AGGGCCACCACCCAC[A/G]AGGCCCCACCAACAT | 58513 |
rs199553377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404551 | GGAAGCCCCTGCCTG[C/T]GCATAGGGCGCTGCC | 58513 |
rs199585528 | snp | A/C/G | 5.24664e-05 | 0.00512156 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418144 | TTACACATCACAGGC[A/C/G]CCGACTCAGCCTGAA | 58513 |
rs199591941 | snp | A/T | 0.000321378 | 0.0126722 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437043 | GGCTGGCACAGAATT[A/T]AATCATAGGTGGGTG | 58513 |
rs199597414 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403341 | ACACACCAGTGGCTG[A/C]GGAGGATGACGTCTG | 58513 |
rs199603624 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393959 | ATTTTACCTGTTGAA[A/G]TTGTCTGCTGTTCTG | 58513 |
rs199675277 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448536 | GAGCAAAATTCCGTA[-/T]TTAAAAAAAAAGGGG | 58513 |
rs199695650 | in-del | -/TCC | 0.0119091 | 0.0762411 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384632 | CCAGCCTCGCTGCTG[-/TCC]TCCTTCAACAGTTCA | 58513 |
rs199710130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366278 | GGTGTAAAGGGAGGA[C/T]GCCCCAGCCAGGCCC | 58513 |
rs199712425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429577 | GCCTCACCAGCCCAC[A/G]CAGCCAAGAGCCTCC | 58513 |
rs199751763 | in-del | -/AA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453887 | AAAAAGAATTCCTAT[-/AA]AAAAAAAAAAAAGGC | 58513 |
rs199776748 | in-del | -/AG | 0.0185938 | 0.0946107 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369124 | TCTGGCTCCCATCTA[-/AG]ACACATGAGGGGAGT | 58513 |
rs199804620 | snp | C/T | 0.00390861 | 0.0440344 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421507 | GCAAAACAGTTAATC[C/T]GGAAGCTTTTTATGA | 58513 |
rs199806239 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450474 | CCCAGGCATGTCCAT[C/T]TTCTTTTTTTTTTTT | 58513 |
rs199816915 | snp | A/G | 0.00299553 | 0.0385849 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358333 | GGCTGTGAGGCCTGG[A/G]AGAGCTCTCCTGAAA | 58513 |
rs199882870 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395403 | TCTTCTGTCTGGAAA[A/G]GATCCGGATGCAACT | 58513 |
rs199906791 | snp | C/G/T | 1.69602e-05 | 0.00291201 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434511 | TGGAAAGAAATAGCC[C/G/T]GAGTAAGTAGGAGAG | 58513 |
rs199918822 | snp | A/G | 0.000131898 | 0.00811982 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16440895 | TTTACCTTCTGGATC[A/G]GCCAAGTCCCATATC | 58513 |
rs199926532 | snp | A/G | 1.69023e-05 | 0.00290704 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425216 | ACGGGGACGGCGCCA[A/G]GGAACACAGTCTTCT | 58513 |
rs199956394 | snp | A/G | 0.000189952 | 0.0097437 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428680 | TTCCTGGGCTGGGTG[A/G]GGAGGAAACAGCAGG | 58513 |
rs199970409 | in-del | -/GAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461649 | AAAGAAAGAAAGAAA[-/GAAA]AGCCAGTTTTCTACA | 58513 |
rs199975794 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377146 | GTTTAGGCCGTGGAG[A/G]AGCAGGTTTCTTCGG | 58513 |
rs199999394 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401647 | GATGTGACCACCTAA[C/G]GAAAAGGTCACACCT | 58513 |
rs200004060 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445494 | CAGCACCAGGCCCCA[G/T]CTGCCACTTCCTCTT | 58513 |
rs200036258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417533 | CTGGATGTGGAGGGA[A/G]GGGCCGTTTCCAACA | 58513 |
rs200099671 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409000 | CCAGAGTGGGAAGAT[-/T]CCCTAGAGGCCAGGT | 58513 |
rs200108602 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472632 | CAACAGAAGCGAAAC[G/T]CTGTCTCAAAAATAA | 58513 |
rs200139528 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461544 | GGAAAATCACTTGAA[A/C]CCAAGAGGCAAAGGT | 58513 |
rs200142581 | in-del | -/A | 0.238749 | 0.249747 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467541 | AAAACAAAAAAAAAA[-/A]CAGGCCAGTGCAGGT | 58513 |
rs200179017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432171 | AGGCACGGTGGCTCA[C/T]GCTTGTAATCCTTGC | 58513 |
rs200214391 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389154 | TTGGAAAAAAAAAAA[-/A]GAAAAGAAAAGAATA | 58513 |
rs200219382 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404674 | CCATCTCGTCCAGGC[A/G]GTCTTGAGCATCCTG | 58513 |
rs200223983 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441479 | GTCTCAAAAAAAAAA[-/A]TTAGCCGGGTGTGGT | 58513 |
rs200246324 | snp | C/T | 0.00346057 | 0.0414525 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417645 | GAACTGTCCTAGAAT[C/T]GAATTCAGAGGCGAG | 58513 |
rs200286494 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423576 | CCTGTCTCTTATATA[-/T]TTTAAAAAAAAAAAA | 58513 |
rs200287491 | snp | C/T | 0.000807841 | 0.0200815 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385161 | AGTCGGCAAAGCCTT[C/T]AGCACTATTGAAGGA | 58513 |
rs200296847 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403344 | CACCAGTGGCTGTGG[C/T]GGATGACGTCTGTTC | 58513 |
rs200306799 | snp | A/G | 0.00194472 | 0.031122 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418147 | CACATCACAGGCGCC[A/G]ACTCAGCCTGAACCC | 58513 |
rs200414981 | in-del | -/A | 0.0807149 | 0.183963 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449593 | TAAAACAACAACAAC[-/A]AAAAAAAACTAAACA | 58513 |
rs200432030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392267 | ACCACACAGAGCAGG[A/C]ACGCAGCTCTCCCGG | 58513 |
rs200434393 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379310 | TCCATCTCAAAAAAT[-/A]AAAAAAAATTAAAAA | 58513 |
rs200435689 | snp | A/G | 2.18081e-05 | 0.00330206 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386274 | AAAAGCAGTTCGTTG[A/G]TTCCATCACCCATTC | 58513 |
rs200451970 | snp | C/T | 8.2659e-05 | 0.00642827 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441928 | GAGGCCAGACTTCTT[C/T]AGAAAAAGCGCAGCT | 58513 |
rs200454287 | snp | A/G | 0.000234169 | 0.010818 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437032 | CATTCCTTTGTGGCT[A/G]GCACAGAATTAAATC | 58513 |
rs200556707 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456590 | TGAACCCAGGAGGCT[-/A]GAGGTTGCAGTGAGC | 58513 |
rs200580041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358324 | GGCACGCTGGGCTGT[A/G]AGGCCTGGGAGAGCT | 58513 |
rs200584074 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412645 | AAAATATATATATAT[-/A]TATTTTTAAAAACTT | 58513 |
rs200609911 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392000 | TAGAGTTGAGGGGTA[-/G]GGAATGGGGATAGAG | 58513 |
rs200621219 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367773 | AAAAAAAAAAAAAAA[A/C]CCAAAAAACAACAAA | 58513 |
rs200621256 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438830 | TGGCTATGTGTTGAA[-/T]TTTTTTTTAAAGCAG | 58513 |
rs200622025 | in-del | -/CAAAAAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400350 | TCAAAAAAAAAAAAA[-/CAAAAAC]AAAAAAAAAAAAAAA | 58513 |
rs200648211 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423580 | GTCTCTTATATATTT[A/T]AAAAAAAAAAATCTA | 58513 |
rs200651044 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469587 | TTACGTTGATATTCA[-/G]GGTCAGAAAAGAGTA | 58513 |
rs200660167 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448539 | GCAAAATTCCGTATT[-/A]AAAAAAAAGGGGGGG | 58513 |
rs200662040 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410148 | AAAAAAAAAAAAAAA[-/A]TGCAATTTAAAAATC | 58513 |
rs200672242 | snp | A/G | 0.000732211 | 0.0191199 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425146 | GAGGCTGCTGACGCT[A/G]CCGTGGGACGGCGTG | 58513 |
rs200742367 | snp | G/T | 1.64879e-05 | 0.00287118 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377239 | AGGAGGAGGTGAAAG[G/T]GCCAGAAGGTGGGGG | 58513 |
rs200766134 | in-del | -/T | 0.030278 | 0.119257 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407309 | CCCCACTCCCCAGCA[-/T]TTTTTTTTTCTTTTG | 58513 |
rs200784345 | snp | A/G | 2.15376e-05 | 0.00328151 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362013 | GAGAAAAAAAAAAGG[A/G]GAAAGAAAGAAATAT | 58513 |
rs200835104 | snp | C/T | 0.232067 | 0.249356 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422971 | TCGGGGAAAAAAAAA[C/T]GGGGGGGGGATTTCT | 58513 |
rs200854798 | snp | A/G | 8.20782e-05 | 0.00640565 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428708 | AGGACTTACCACAGC[A/G]AACTCATCTCGATCC | 58513 |
rs200858025 | snp | C/T | 0.00184974 | 0.0303554 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385104 | ACACTAGCAGAGGCG[C/T]GGGGGCTCCGTGGAG | 58513 |
rs200865144 | snp | A/C/G | 0.000100315 | 0.00708162 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417954 | ACCACTCACCGGGCC[A/C/G]GGCGTGCCTCTCTCC | 58513 |
rs200935142 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433347 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCCTGAC | 58513 |
rs200939092 | in-del | -/C | 0.0766824 | 0.180169 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417462 | CCTGTGATGAGCAAA[-/C]TTCCAGGTGAGCCTC | 58513 |
rs200984218 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413791 | CACCTCGCTGGTTTT[C/T]TGTCTGATTGCCTCT | 58513 |
rs201017085 | snp | C/G | 0.115438 | 0.210697 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461545 | GAAAATCACTTGAAC[C/G]CAAGAGGCAAAGGTT | 58513 |
rs201091846 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376163 | GCATGATCCTGGGAG[G/T]GCGTGGGTCTCCTGT | 58513 |
rs201102412 | snp | A/G | 0.000364492 | 0.0134949 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417970 | GGCGTGCCTCTCTCC[A/G]AAGGCGGGACCATGT | 58513 |
rs201175190 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417590 | ACTGATGTCATCAAG[C/T]TCCTTCACGCCAGTA | 58513 |
rs201186903 | snp | C/G/T | 3.30607e-05 | 0.00406565 | synonymous-codon, missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441958 | TTCACTCGCCCCCAC[C/G/T]CTCCCTGTGTATGCC | 58513 |
rs201203201 | snp | A/C/T | 0.000411879 | 0.0143447 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425350 | ATGGCACTGAAGGGG[A/C/T]AAGGCTGGGGCCGGG | 58513 |
rs201216751 | snp | C/T | 0.000165243 | 0.00908813 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404577 | CTGCCCCGGAGGTGG[C/T]CGGGACCCACCATCT | 58513 |
rs201248785 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456204 | AAACCCTGTCTCAAA[A/C]AAACAAACAAAAAAC | 58513 |
rs201257012 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428600 | AAAGAAAAGAAAAGA[A/G]AAAAGAAAAGAAAAA | 58513 |
rs201291280 | snp | C/T | 0.00012016 | 0.00775021 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434531 | AAGTAGGAGAGCACA[C/T]CTGTGTGAATGTCCA | 58513 |
rs201335787 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390851 | ACATGTAAAGCAGTG[C/T]TTAAGGGAAATATGT | 58513 |
rs201367089 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467619 | AGTGGATTTTACTCT[-/A]AAACTTCGTTCTCAT | 58513 |
rs201394637 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398995 | AAGGTTTTTTTTTTT[-/T]CAGTGTTTTCAGTCG | 58513 |
rs201406459 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450958 | AAATGGTACAGGCTC[-/T]TTTTTTTTTGAGACA | 58513 |
rs201411100 | snp | C/T | 0.000116849 | 0.00764269 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425066 | AGAGGGGGCTGTGCC[C/T]GCTGAGGGCTCCGTA | 58513 |
rs201420017 | snp | A/C/G | 8.28787e-05 | 0.00643687 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437011 | CGTGCTGAGAAGAGA[A/C/G]AGAAACATTCCTTTG | 58513 |
rs201467796 | snp | C/T | 0.00196438 | 0.0312783 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418126 | GAAACGTGGGGATGC[C/T]AATTACACATCACAG | 58513 |
rs201487904 | snp | A/G | 0.00299553 | 0.0385849 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358332 | GGGCTGTGAGGCCTG[A/G]GAGAGCTCTCCTGAA | 58513 |
rs201589755 | in-del | -/GAGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428481 | GAGGAGAGAGGGAGA[-/GAGG]GAGGGAGGGAGGGAG | 58513 |
rs201602551 | snp | A/G | 6.60208e-05 | 0.00574509 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417988 | GGCGGGACCATGTCC[A/G]GCGAGAGGACTTGAG | 58513 |
rs201632135 | snp | A/C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420814 | AGAGGGGTTGAGGCC[A/C/G]ACTCCTCGACTGGGC | 58513 |
rs201647819 | snp | C/T | 0.00129064 | 0.0253704 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404568 | CATAGGGCGCTGCCC[C/T]GGAGGTGGCCGGGAC | 58513 |
rs201650842 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373708 | TACAGAGCCCGGCTC[-/T]TGATTCCCTTGACCA | 58513 |
rs201668616 | in-del | -/TT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439925 | GTTTCAGATTTCAGA[-/TT]TTTTTTTTTTTTTTT | 58513 |
rs201688000 | snp | G/T | 0.000408547 | 0.0142866 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425348 | CAATGGCACTGAAGG[G/T]GCAAGGCTGGGGCCG | 58513 |
rs201753082 | snp | A/G | 0.000560538 | 0.0167319 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440938 | AAAATGCTCATAAGC[A/G]TGACTGCCGATCACT | 58513 |
rs201762498 | in-del | -/CTAA | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368713 | AACACAGACACCCAC[-/CTAA]CTGTCATTCACCCTA | 58513 |
rs201768020 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464767 | TAACACTAACACTAA[C/T]ACTAATGATAGCTGA | 58513 |
rs201784509 | snp | A/C | 0.000233493 | 0.0108024 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434336 | CAGGGACACTGAGTG[A/C]AGAAGAACCAAGCCC | 58513 |
rs201804789 | snp | A/G | 0.000173862 | 0.00932205 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377080 | GTCCCCCGCCATCCG[A/G]CACCGGTAGGCGGTG | 58513 |
rs201823107 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409060 | GACCCTGTCTCTTAA[-/C]AAAAAAAAATTGTTT | 58513 |
rs201830738 | snp | C/T | 8.33799e-05 | 0.00645624 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425174 | GTGGAGCGGAGGCTG[C/T]CTTTTGGTGGGGGGC | 58513 |
rs201944410 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391640 | TTTTTTTTTTTTTTG[A/C]TTTTGAAATCCAAGT | 58513 |
rs201951183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435380 | TGTTCTGAAAGACAT[A/G]GGGCAGGCAGCCCGT | 58513 |
rs201989047 | snp | A/G | 0.00128921 | 0.0253563 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386270 | AGTAAAAAGCAGTTC[A/G]TTGGTTCCATCACCC | 58513 |
rs202010883 | snp | A/G | 0.000233244 | 0.0107966 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402452 | TGTGGGCCTCCTGGC[A/G]GCTTTCATGCAGCTG | 58513 |
rs202016723 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436408 | GCAGTAGCTTATCTT[A/G]CCAGCCACAACATCC | 58513 |
rs202076491 | snp | C/T | 0.000198364 | 0.00995703 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385102 | AGACACTAGCAGAGG[C/T]GCGGGGGCTCCGTGG | 58513 |
rs202085014 | snp | A/T | 0.078151 | 0.181571 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423581 | TCTCTTATATATTTA[A/T]AAAAAAAAAATCTAT | 58513 |
rs202116916 | in-del | -/AAATAC | 0.114823 | 0.210303 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432588 | AATAAATAAATAAAT[-/AAATAC]AAATACAAATACAAA | 58513 |
rs202120798 | in-del | -/A | 0.078151 | 0.181571 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423580 | GTCTCTTATATATTT[-/A]AAAAAAAAAAATCTA | 58513 |
rs202167953 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436981 | GCGGTGTGACCATCA[A/G]AGGGCTGCTGGTGTC | 58513 |
rs202179516 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434131 | CACCTCCTCATCTGT[A/G/T]AAGTGGAAGGATTCT | 58513 |
rs202209452 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455891 | CAGCTACTGACCTCC[C/T]CCCACCCTTCGCATA | 58513 |
rs202216301 | in-del | -/AGGTG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417467 | GATGAGCAAACTTCC[-/AGGTG]AGCCTCTGATATTTC | 58513 |
rs202223851 | in-del | -/ATAATAATAATAATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393078 | CTGCAGGAGCTGGAT[-/ATAATAATAATAATA]ATAATAATAATAATA | 58513 |
rs202246804 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400359 | AAAAACAAAAACAAA[-/C]AAAAAAAAAAAACCC | 58513 |
rs367639509 | snp | G/T | 0.000183688 | 0.00958178 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425354 | CACTGAAGGGGCAAG[G/T]CTGGGGCCGGGACCA | 58513 |
rs367640832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399020 | TCAGTGTTTTCAGTC[A/G]TCACTTGGAAGACTG | 58513 |
rs367656878 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431217 | GCACTCCAGCCTCGG[C/T]GACAGCGAGACTTCA | 58513 |
rs367670862 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453808 | TCATGCAATACTCTC[A/G]TGTAACAAATATGCA | 58513 |
rs367690687 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398326 | CACAGGGTTTTCCCA[A/G]GGTGGGGAAACCAAG | 58513 |
rs367752435 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414132 | CCCAAGTGTGATAAG[A/G]ACCCAGAGCGCCCTT | 58513 |
rs367797741 | snp | A/C | 3.30644e-05 | 0.00406585 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436921 | GCCAAGGAGGGAGCT[A/C]TTCCCGTTCACTTAC | 58513 |
rs367827551 | snp | A/G/T | 3.40057e-05 | 0.00412333 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377101 | GTAGGCGGTGGCTGC[A/G/T]AGAGAAGAAAGCTTA | 58513 |
rs367838777 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437528 | ATGGGGTCTCCTTGC[A/G]GAGGGATGAAAAAGT | 58513 |
rs367847672 | snp | C/T | 0.000264031 | 0.0114868 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440806 | AGCCGTGGAGGTCAC[C/T]CAGCCTGGGGGCTCT | 58513 |
rs367851550 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381541 | GGAAATGAGGTGCCA[C/T]GTGACAGGCATCAGT | 58513 |
rs367867461 | snp | A/G | 4.94613e-05 | 0.00497275 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392399 | CAGTGGCAGAGCCAC[A/G]GAATGGGTCACTTTC | 58513 |
rs367868341 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447984 | TCTTGACAAAGGTGC[A/G]AAAGTATTTCAGGAG | 58513 |
rs367877283 | snp | C/T | 0.00011725 | 0.0076558 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417953 | CACCACTCACCGGGC[C/T]GGGCGTGCCTCTCTC | 58513 |
rs367891749 | snp | A/C | 3.34174e-05 | 0.00408749 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392456 | CTAGAAGGAAAAATG[A/C]CCCATAAGTAAACAT | 58513 |
rs367892495 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414896 | TTATTTTTTGTAGCC[A/G]AGGTCTCAATATATG | 58513 |
rs367905390 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383920 | CGAGGGGGCCTCATG[C/G]CTGGGGCACGCGTCT | 58513 |
rs367927721 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393829 | ACATGGATGGACGGC[C/T]GTCCTTCCCAGTTAC | 58513 |
rs367934588 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423796 | AGAAGCCAGGGATCA[C/T]AAAGAGGTAACAGGA | 58513 |
rs367956383 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409797 | ACAAAAATTAGCTGT[A/G]TGTGGTGGTGCACAC | 58513 |
rs368035210 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451818 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCTACAA | 58513 |
rs368036687 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430217 | CTCCCCGTGCTCGAG[C/T]GGGTCAGGGGCCCTC | 58513 |
rs368055626 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378205 | GACGTCTTGCAGGTA[C/G]GTAGGTAGGTAGGCA | 58513 |
rs368061771 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361746 | GCAAGCGGAAGGGAG[C/T]GGGGTGGCCCGGAGG | 58513 |
rs368075194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464634 | AGTCCTCTTTGCCTC[A/C]GTGTGAAAGGCTATT | 58513 |
rs368081143 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457016 | TATGAGATGGTAAAC[A/G]GCAGAAATCCGCTGC | 58513 |
rs368103763 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399294 | TACAAAGATACCATC[A/G]ACTCTACCCCTTGCA | 58513 |
rs368177133 | in-del | -/G | 0.108402 | 0.206034 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428556 | AAGACAGAAAAGAAA[-/G]GAAAAGAAAGGAAAA | 58513 |
rs368177768 | in-del | -/A | 0.494315 | 0.0530107 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395202 | CGAGAGTTCGTCTCC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs368178606 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388668 | CGTCTCTACTAAAAA[-/A]TACAAGAAATTAGCT | 58513 |
rs368232439 | snp | A/G | | | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425242 | CTTCTTTCTCTTGGA[A/G]GGTGGGATGAGGGAC | 58513 |
rs368232459 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448550 | TATTAAAAAAAAAGG[C/G/T]GGGGGGAGAAAGGCC | 58513 |
rs368246957 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467430 | GCTAGGATTACAGGC[A/G]TCAGCCACTGCACCC | 58513 |
rs368268891 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381827 | CCTGGGCCTAGGGCC[C/T]GTGCGAGTCCCCCGC | 58513 |
rs368301891 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429758 | TGCACCCCAACCCAG[A/C]CTCCACAGACTCCAC | 58513 |
rs368331807 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405434 | CTGAAGCTCTCTCTG[A/G]CCCCGTGGGATGGAT | 58513 |
rs368339299 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462687 | AAAAATAAAGTAAAA[A/C]AAAGAATCAGGGAAG | 58513 |
rs368354071 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412880 | ATAAGGAGTGGATGC[C/T]CATCACCAAGCTGGG | 58513 |
rs368373962 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472305 | TCTCTGTTAGGGATG[C/T]CGTCCCCCTGCCAGT | 58513 |
rs368402926 | snp | C/T | 4.94434e-05 | 0.00497184 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404620 | GGCACTTCTGCCGGA[C/T]GTCGCTCAGCATGTC | 58513 |
rs368415676 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369415 | AACAAATATTTACTA[C/T]GAGCCACTGCTGGCC | 58513 |
rs368429201 | snp | A/G | 1.8871e-05 | 0.00307166 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386145 | CCAAGGAATAGTCAG[A/G]AAGAAAAATAAGTCA | 58513 |
rs368455310 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461748 | TCTGATGAGCGGAGG[G/T]GAGGAGGTAGCAGGG | 58513 |
rs368473067 | snp | A/G/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404639 | GCTCAGCATGTCTCG[A/G/T]AGCTTGGCCTTCTGC | 58513 |
rs368488054 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376706 | GGCCCTCCCTGAGCA[C/T]GGACAGGGAGAAGGA | 58513 |
rs368488259 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400361 | AAAACAAAAACAAAA[A/C]AAAAAAAAAACCCCT | 58513 |
rs368533262 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430401 | CATCCCTTCTCCACC[A/C]TTCCACAACTGTGCA | 58513 |
rs368631545 | snp | A/G | 0.000247412 | 0.0111196 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392281 | GCACGCAGCTCTCCC[A/G]GGCAACGTCCCACCC | 58513 |
rs368674405 | snp | C/T | 0.000958189 | 0.0218672 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425284 | GGAGGGCACGGGCTC[C/T]TTCTCCAGGGCTCGG | 58513 |
rs368688631 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367019 | CAAAAGCTGCCACGC[A/G]CACCCACGCCAGGGT | 58513 |
rs368691237 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393542 | TAGTCCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 58513 |
rs368709048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435957 | AGTATAAGATCTCTT[A/G]GCACTGTTTCCCATG | 58513 |
rs368728491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386110 | TGAAAGTGTTAACTG[C/T]GGGGGAGCTCTGCTA | 58513 |
rs368734689 | in-del | -/GCA | | | intron-variant, cds-indel | EPS15L1 | GRCh38.p7 | 19:16401334 | AAAGAAACACATCAA[-/GCA]TTGAACATAAAGAGG | 58513 |
rs368904330 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457824 | CTCTGACCCATGAGC[A/G]GTCTCCCTGGAGAGA | 58513 |
rs368934453 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380412 | CATGCAGATGCAGCC[A/G]TCTAGGCTTCTAGCG | 58513 |
rs368949292 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421235 | CAGGCTGGAGGGGGC[C/T]CCCTGACCACCACCC | 58513 |
rs369017043 | in-del | -/AA | 0.081446 | 0.184634 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428515 | GGGAGAGAGAGAGAG[-/AA]AGAAAGTGAAAGAAA | 58513 |
rs369017942 | snp | C/G | 0.000132262 | 0.00813102 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377281 | GACATGAAAGAGAGG[C/G]AAAAATAGTTGTTAA | 58513 |
rs369030341 | snp | A/T | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403746 | ACCTGGTTGATTTCG[A/T]CTTGCGTTGACTTCA | 58513 |
rs369047331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394998 | GCTGAGGCGGGTGGA[C/T]TACCTGAGGTCAAGA | 58513 |
rs369048907 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386801 | TAGCTGAGGCCACAA[A/G]AACTGAGCTGGGATT | 58513 |
rs369132398 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408234 | GAGCTCAGAGCAAAA[-/G]AGAAGACAAAAATAA | 58513 |
rs369243617 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432172 | GGCACGGTGGCTCAC[A/G]CTTGTAATCCTTGCA | 58513 |
rs369259509 | snp | A/G | 1.69893e-05 | 0.00291451 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442032 | AGCAAATGCAGCAGC[A/G]GGTGAAGTGGCACCC | 58513 |
rs369267736 | snp | C/T | 1.68286e-05 | 0.0029007 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392471 | CCCCATAAGTAAACA[C/T]TATACCAAGTGAAAG | 58513 |
rs369274991 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392305 | CCCACCCCACTCACC[C/T]TCGAAGGTAAGGAAG | 58513 |
rs369284918 | snp | C/G | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377214 | TCATCTGAGAATCCT[C/G]CCCCTCCCAAGGAGG | 58513 |
rs369286988 | snp | A/G | 1.66701e-05 | 0.002887 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437026 | GAGAAACATTCCTTT[A/G]TGGCTGGCACAGAAT | 58513 |
rs369307683 | snp | C/T | 1.66416e-05 | 0.00288453 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425142 | TGTTGAGGCTGCTGA[C/T]GCTGCCGTGGGACGG | 58513 |
rs369310759 | snp | C/T | 0.000446744 | 0.014939 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402272 | GATGTTCTGCTGTCA[C/T]ACCAGGGGACCAGAG | 58513 |
rs369425032 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469357 | AGTTCGAGGAGGATC[A/G]GCTGCAGCCACAGGG | 58513 |
rs369431809 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450099 | ACAAAAAAAAAAAAA[A/T]AGCCACGCATGGTGG | 58513 |
rs369450961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422229 | TTGAGAGAGGCAAAC[A/G]CCATCATGGGTCAAC | 58513 |
rs369471419 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465005 | AATGGCATGAACCCA[A/G]GAGGCGGAGCTTGCA | 58513 |
rs369478104 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405996 | GGGTCCAGGGAGAGG[A/C]AGCAGCAGCTGGGGC | 58513 |
rs369501571 | snp | A/G | 0.000125867 | 0.00793206 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361763 | GGGTGGCCCGGAGGC[A/G]GAGGACTCAACTTAC | 58513 |
rs369546255 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459533 | GTTGGTAGTGGGGAG[A/C]GGGCAGACATAGCTC | 58513 |
rs369548061 | in-del | -/GT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355621 | AGTACGGTGGCGACG[-/GT]GTGTGTGTGTATATA | 58513 |
rs369551491 | in-del | -/A | 0.400147 | 0.19989 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362377 | CAAGCTTCTAACAGT[-/A]AAAAAAAAAAAAAGG | 58513 |
rs369613524 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364762 | TCCACTGGAGCAGAA[-/G]GGGGCTCCCTAGGGC | 58513 |
rs369631521 | in-del | -/AGAAAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428551 | GAAGAAAGACAGAAA[-/AGAAAG]GAAAAGAAAGGAAAA | 58513 |
rs369675832 | snp | A/G | 0.000131776 | 0.00811608 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395424 | GGATGCAACTCTTGC[A/G]TGTTGTTGCTAAATA | 58513 |
rs369696486 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394433 | GGCACCCCTGGGCTT[C/T]AGGGGCTGCCAGATT | 58513 |
rs369718275 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358640 | AGCCTCTTGGAAATC[C/T]GCAGTTTAGACAGCT | 58513 |
rs369722373 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437967 | AGAGGATGTGCACTT[A/C]AACAATGAAGGCCGT | 58513 |
rs369747349 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432687 | TGAGGCAGGAGAATT[G/T]CTTGAACCTGGGAGG | 58513 |
rs369753941 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402728 | AACAAACCAAGACCC[A/C]TCTCTGCAAAAAATA | 58513 |
rs369755619 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419288 | ACATGGGGAAATCCC[A/G]CCTCTACTAAAAATA | 58513 |
rs369757727 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441629 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs369783739 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355954 | CAGGGTCCTGCCCAC[C/T]GCCCAGCGGAGGGTC | 58513 |
rs369835527 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413782 | CCTTACCTGCACCTC[A/G]CTGGTTTTCTGTCTG | 58513 |
rs369849069 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16440909 | CGGCCAAGTCCCATA[C/T]CTGCGGAAACACAAA | 58513 |
rs369873713 | snp | A/G | 0.00016749 | 0.0091497 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403914 | TGAGATTGGATTTGC[A/G]TTTTCAGTGATGAGA | 58513 |
rs369903435 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460074 | AAGGTCAGGAATTCA[A/T]GACCAGCCTGGGCAA | 58513 |
rs369921834 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374437 | CAGCTCCCTAAAAAG[C/T]CTGAACCCTGAAGCC | 58513 |
rs369929887 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455894 | CTACTGACCTCCCCC[C/G]ACCCTTCGCATAAAA | 58513 |
rs369934694 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468289 | GCCAAGAGCCAGAAG[G/T]GCAGGAAAGGGACCC | 58513 |
rs369934760 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395187 | CTGACAGCAAGAGAG[C/T]GAGAGTTCGTCTCCA | 58513 |
rs369940098 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410976 | ATAAAAAGGAATTCA[A/G]CGCTAATATATGCTA | 58513 |
rs370040435 | in-del | C/GAGATTA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395936 | GGCGATAGAGTGAGT[C/GAGATTA]TATCTCAAAAAAAAA | 58513 |
rs370094877 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456572 | TGAGGCGGGAGAACC[A/G]CTTGAACCCAGGAGG | 58513 |
rs370116075 | snp | C/T | 3.32723e-05 | 0.00407861 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418086 | TAACTTCCCCGTTTG[C/T]CTCGTATCGGCCAGG | 58513 |
rs370122755 | snp | C/G/T | 3.29518e-05 | 0.00405894 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421389 | CCTCCTGGCCACTCA[C/G/T]GTAGCCATCCAGGTC | 58513 |
rs370160797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382007 | CTCTGTGTCGCGCAA[C/T]AGGACCCGGGCAATA | 58513 |
rs370167441 | snp | A/G | 1.6534e-05 | 0.00287519 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404572 | GGGCGCTGCCCCGGA[A/G]GTGGCCGGGACCCAC | 58513 |
rs370193867 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421635 | TGTGATCCTTGTTCT[A/G]TAACTGGCAAAACTG | 58513 |
rs370241773 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370617 | GGATCCGCCTCTGGG[C/T]ACAGTGTGCCCAGGA | 58513 |
rs370254755 | in-del | -/ACACCATT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448485 | AGGTGAGCCGAGATC[-/ACACCATT]GCACCATTGCACTCC | 58513 |
rs370279365 | snp | A/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402185 | GAACGCGCAAAGTGG[A/C]AGCAAAAACAACAGA | 58513 |
rs370297562 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447924 | ATGCACAGAACAGAA[C/T]GTAGAATCTGAGAAA | 58513 |
rs370314258 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473946 | TTTGGGCAACAAGAG[C/T]GAAACTCCGTCTCAA | 58513 |
rs370342329 | in-del | A/GG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448557 | AAAAAAGGGGGGGGG[A/GG]GAAAGGCCGGGCGCG | 58513 |
rs370396791 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460799 | CTGGGACCCCCCAAC[C/T]ACAAACAGTGCCATT | 58513 |
rs370404016 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407125 | CTCCCAGTGCATGGT[A/G]TGCTGTTATGGCAAG | 58513 |
rs370407737 | snp | G/T | 0.000217146 | 0.0104176 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421516 | TTAATCTGGAAGCTT[G/T]TTATGACCCCCAGAC | 58513 |
rs370432975 | in-del | A/CCC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400502 | TCAGGGACCTAAAAC[A/CCC]CAACTTCGACCCACA | 58513 |
rs370451594 | snp | C/G | 1.75029e-05 | 0.00295823 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441847 | CCTGCGGGGGGAGCT[C/G]TGAGGGCAGCCACAG | 58513 |
rs370455852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440729 | AAATGAAAACTTCCC[A/G]TGTTAAGTTTGACAG | 58513 |
rs370464358 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379689 | ATCTAAGGCTCCAGC[A/G]TTTAGTCACACCAAT | 58513 |
rs370482356 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384071 | ATGGGCTCCAGGAGG[A/G]GGGCTGTGTTCTGCT | 58513 |
rs370484313 | snp | C/T | 1.6522e-05 | 0.00287414 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385110 | GCAGAGGCGCGGGGG[C/T]TCCGTGGAGGGGCTT | 58513 |
rs370497219 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451630 | ACCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 58513 |
rs370508443 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372319 | CACACTGCATGCCAG[A/C]CACACCAAATGTCAA | 58513 |
rs370517056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401094 | ATGCTCATCGTTTAA[A/G]TTTAGACGATAAAGC | 58513 |
rs370558804 | snp | C/T | 4.99929e-05 | 0.0049994 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418089 | CTTCCCCGTTTGCCT[C/T]GTATCGGCCAGGGCC | 58513 |
rs370620443 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385044 | ATACATACGTGACAT[-/G]AACAATTACGCCTGG | 58513 |
rs370650916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376618 | CAATCTCCCGCTCCC[C/T]CCACTCTCAGTCCTG | 58513 |
rs370655075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464996 | AGGCAGTAGAATGGC[A/G]TGAACCCAGGAGGCG | 58513 |
rs370656858 | snp | C/G/T | 0.000121532 | 0.00779439 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377084 | CCCGCCATCCGGCAC[C/G/T]GGTAGGCGGTGGCTG | 58513 |
rs370688830 | in-del | -/A | 0.296364 | 0.245663 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431236 | GCGAGACTTCATCTC[-/A]AAAAAAAAAAAACTT | 58513 |
rs370694875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419316 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCGCGC | 58513 |
rs370720059 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461031 | CCAGCTGGGGCCAGG[C/T]GCGGTGGCTCACGCC | 58513 |
rs370747100 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410756 | TCGCTGCAAAAAAAA[-/A]TTAAAAATTAGCCAA | 58513 |
rs370780807 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393372 | AAATAAATCGGTCGG[C/G]CATGGTGGCTCACGC | 58513 |
rs370804943 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421284 | GGCCCCCTGGAGCCA[-/C]CCCACAGCCACAACT | 58513 |
rs370805862 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367569 | AATTTCTTTAATTCT[C/T]CTATTTCTCAAGCTT | 58513 |
rs370823657 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415590 | CCCTTGCTGGCTTAT[A/G]GCAGTGTGAAATCAT | 58513 |
rs370830808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447063 | CCTTCCCCTTAGAGG[C/G]CCCCACAGGCCTTGC | 58513 |
rs370834902 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452051 | GGCTGAGGCAGGAGA[A/C]ATGCTTAAACCCAGG | 58513 |
rs370846941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359195 | ACGCTGAAAGAGTCA[C/T]GCTGCCAATCTGCCG | 58513 |
rs370875662 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401550 | CGGCCCATCCGCTCC[C/T]GGAACAGCACCAAGA | 58513 |
rs370883650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435603 | ATCACCGGCAGACAC[C/T]GCATGCTTTCACAGC | 58513 |
rs370889778 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393529 | TAGCGGGCGCCTGTA[A/G]TCCCAGCTACTTGGG | 58513 |
rs370990400 | snp | A/G | 1.92446e-05 | 0.00310193 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425258 | GGTGGGATGAGGGAC[A/G]GGGGCAGGGCGGAGG | 58513 |
rs370996327 | snp | C/T | 0.000151087 | 0.00869025 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361883 | CCCCAAACCCCTTTT[C/T]ACTTTGGAACGGGTC | 58513 |
rs371006895 | snp | C/G/T | 1.6628e-05 | 0.00288335 | synonymous-codon, missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402342 | TCCAAAACTGCCCCT[C/G/T]TCTGCCAGGGAGACG | 58513 |
rs371007291 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441837 | CTGGCCCTGACCTGC[C/G]GGGGGAGCTGTGAGG | 58513 |
rs371026457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397235 | GCTGGGATTACAGGC[G/T]TGCACCACCATGCCC | 58513 |
rs371061868 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376828 | CAGGCGGAGGCCGCA[A/C/T]GAAGCGCCCCCAGCC | 58513 |
rs371073078 | snp | A/C | 6.46238e-05 | 0.00568399 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428664 | CGCACTGCACATTTC[A/C]TTCCTGGGCTGGGTG | 58513 |
rs371091644 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456683 | CAAAAACAAAACAAA[-/A]CAAAAAATAGAGTCC | 58513 |
rs371100910 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406823 | TCACTGGCCACATGC[C/T]GTGTACTGAATGTCT | 58513 |
rs371118355 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451203 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 58513 |
rs371166145 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457883 | GGGGAGGGGGGAACA[A/C]CGAGAGGGGCTCAAT | 58513 |
rs371196544 | snp | A/G | 4.9525e-05 | 0.00497595 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413758 | AGATGTAACCAAAAC[A/G]AACGAGACCCTTACC | 58513 |
rs371226116 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414711 | GCCTTTTTTTGGTTT[G/T]GTTTTTTTTTTTTTT | 58513 |
rs371236950 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393667 | AAAAAAAAAAATAAA[A/T]AATAAATAAATAAAT | 58513 |
rs371252295 | snp | C/T | 0.000798639 | 0.019967 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361754 | AAGGGAGTGGGGTGG[C/T]CCGGAGGCGGAGGAC | 58513 |
rs371273945 | snp | C/T | 4.99222e-05 | 0.00499586 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425078 | GCCCGCTGAGGGCTC[C/T]GTACCTGTGTTTGCT | 58513 |
rs371290939 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412940 | CCCTGGAGGAGAGCT[A/G]TCTCTTCTCCCGCCC | 58513 |
rs371293999 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444171 | GGAGAGGGAAAAAGT[A/C]AAAAAAAAAAAAAAG | 58513 |
rs371374478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454352 | TGGCTTATAAGCACA[C/T]GGTATCCTATCGCCC | 58513 |
rs371397272 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360589 | CTACAAAAAAAAAAA[-/A]ATTAAACATTAGCCT | 58513 |
rs371425737 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409654 | CTTCAAATTCAGCTA[C/T]AGGCCAGGCGCAGTG | 58513 |
rs371427043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464022 | CAGGCCTGGGAAACA[C/T]GGGGAGCAGGTGTGC | 58513 |
rs371434075 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368338 | CACAACAGGGGACAC[A/G]CATGCACAAGCATCA | 58513 |
rs371450906 | snp | A/G | 5.21399e-05 | 0.00510561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417900 | CACCTGGTGGCAGGC[A/G]GTGGGAAGGGATGTC | 58513 |
rs371480880 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398346 | GGGAAACCAAGCCGG[C/G]TTCTTAGACAAGTTA | 58513 |
rs371507057 | in-del | -/AAAG | 0.118584 | 0.212673 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461626 | ACTCTGTCTCAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 58513 |
rs371515390 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442561 | TCAGAGGGAAAGGAC[A/C]CTCTATCCTCTGAGA | 58513 |
rs371628165 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464729 | GGGCCACACATAAAA[A/T]ACACTAACACTAACA | 58513 |
rs371635442 | snp | A/G | 8.24613e-05 | 0.00642058 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392286 | CAGCTCTCCCGGGCA[A/G]CGTCCCACCCCACTC | 58513 |
rs371679874 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374238 | GGCCTGTCTCCCTCA[C/T]GGGTCTTGCTGGGAC | 58513 |
rs371691909 | in-del | -/TT | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354932 | GGCTTATGGGAACTC[-/TT]TGTATCTTTGTGATT | 58513 |
rs371696682 | snp | A/G | 0.000263535 | 0.011476 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393995 | GGGTCATTCTGGAAC[A/G]GGTCGCCTGGTTGGA | 58513 |
rs371699909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415131 | GCCACAAGGCCCAGG[A/G]TTTAGTGCCCTTATA | 58513 |
rs371709529 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362763 | CATCTGCCCGCCTCA[C/G]CCTCCCAAAGTGCTG | 58513 |
rs371775479 | snp | A/G | 6.59761e-05 | 0.00574314 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392406 | AGAGCCACGGAATGG[A/G]TCACTTTCTTTGAAA | 58513 |
rs371820931 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444171 | GAGAGGGAAAAAGTC[-/A]AAAAAAAAAAAAAAG | 58513 |
rs371858696 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418053 | GAAATACATAGCTAA[C/T]GCGAATTGGTCTTTG | 58513 |
rs371862540 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420151 | TAGACTTCTTTTCTC[A/G]TGGTTATTCAAGAGC | 58513 |
rs371880479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377544 | GCATCCCCAGTCACA[C/T]GAGGCACACTGGGTC | 58513 |
rs371882273 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464801 | GCTTTAAAAAATTCA[C/T]GGGTGGGCATGGTGG | 58513 |
rs371897669 | snp | C/G | 4.94768e-05 | 0.00497352 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377173 | TCGGAGGCAGAGCAG[C/G]AGTGTCCTGTTTACT | 58513 |
rs371897816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417215 | GACCACACAGCTGCC[A/C]CGGGCTCTGCCCACG | 58513 |
rs371902502 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419592 | GAGGGACCTCGTTTC[C/T]CACCTCCCGTGTAGC | 58513 |
rs371903110 | snp | C/G/T | 5.19245e-05 | 0.0050951 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417912 | GGCGGTGGGAAGGGA[C/G/T]GTCAATACCCCCAGG | 58513 |
rs371909358 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364875 | CACCAGCTCGGCTCC[C/G]TTCCCTGTGAGCCAA | 58513 |
rs371917778 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387653 | TGCCTGTAATCCCAG[C/G]TACTCAGGAGGCTAA | 58513 |
rs372029791 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402960 | ACTGAAAGTAATCCT[A/T]CAGATATTAACCATA | 58513 |
rs372032690 | snp | A/G | 8.40704e-05 | 0.00648291 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404775 | GTTGCAGGGGTTTAC[A/G]TGAGGATGGGAAAAA | 58513 |
rs372076114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423827 | GTCAGACAAGCTGAG[C/T]TGTGGCGGGACACAG | 58513 |
rs372085731 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381618 | TGATCACACCAAGTA[C/T]GAAGCTGCGATTGGA | 58513 |
rs372091536 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360682 | AGCCCAGGAATTCGA[A/G]GTTACAAGTGAGCTC | 58513 |
rs372129351 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373235 | CGCCAGGCTCACAGG[A/G]GGTCGCATTTCACCT | 58513 |
rs372200117 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396945 | GGCTGCCAGGGGCTG[-/T]GGGTGGGGGGATGGG | 58513 |
rs372238257 | snp | C/T | 0.000236598 | 0.010874 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392477 | AAGTAAACATTATAC[C/T]AAGTGAAAGAACCCA | 58513 |
rs372294525 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428829 | GTGAGACCACCTGCC[A/G]GAACTCAGACTCTCA | 58513 |
rs372298217 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452898 | GCCTCCCCGGTTCAT[A/G]CCATTCTCCTGCCTC | 58513 |
rs372334211 | snp | A/G/T | 4.94224e-05 | 0.00497083 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393933 | CTAAAGACCGGTCCG[A/G/T]GAAACACTGAATTTT | 58513 |
rs372376256 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457637 | TGGAACTGGAATGGC[A/G]CCCGGGCAGGAGGGG | 58513 |
rs372409006 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452860 | GGAGCGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 58513 |
rs372459946 | snp | C/T | 1.71358e-05 | 0.00292704 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361851 | GGGGACAAATGGGTC[C/T]TTTCCACTAAACGGG | 58513 |
rs372467299 | snp | A/G | 1.69029e-05 | 0.00290709 | synonymous-codon, missense, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361971 | ACCAAGCTGGCTTAC[A/G]GGTGTACTTTTACCT | 58513 |
rs372478910 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381883 | TCTAGATGGGAAGTG[C/G]TGTGACCGGCTGGGC | 58513 |
rs372508017 | in-del | -/AC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432592 | AATAAATAAATAAAT[-/AC]AAATACAAATACAAA | 58513 |
rs372511030 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403214 | GGGCAACGGCTGCAG[A/G]CCACGAGAAGCCAGC | 58513 |
rs372537893 | snp | A/G | 0.000104992 | 0.00724467 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361737 | AGGGAAGCTGCAAGC[A/G]GAAGGGAGTGGGGTG | 58513 |
rs372563166 | snp | C/G | 1.65072e-05 | 0.00287286 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437751 | GAAGAATGTGAACTT[C/G]AAGGACTTGGACACT | 58513 |
rs372687715 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357305 | TGGGGAGCAGGATAC[C/T]AGGTGAAACTGACAG | 58513 |
rs372694523 | snp | G/T | 3.32353e-05 | 0.00407634 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377127 | GCTTACTGACCGCTG[G/T]GCGGTTTAGGCCGTG | 58513 |
rs372722067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452083 | GGCGTAGGTTGCAGT[C/G]AGCCAAGATCACGCC | 58513 |
rs372738974 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400362 | AAACAAAAACAAAAA[A/C]AAAAAAAAACCCCTG | 58513 |
rs372751665 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399005 | TAAGGTTTTTTTTTT[-/T]CAGTGTTTTCAGTCG | 58513 |
rs372771944 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388036 | CTGACAGCTGAAAGC[C/T]TACCAAATTTGTTTT | 58513 |
rs372777500 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472306 | CTCTGTTAGGGATGC[C/T]GTCCCCCTGCCAGTG | 58513 |
rs372779727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449659 | TGGGCATTTACCCGG[A/G]AGAAATGAAGAGTCA | 58513 |
rs372782621 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367306 | ACCCTCTTGGGTGTG[C/T]TGACTGCCTACCGCA | 58513 |
rs372803001 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363498 | TAAAGCCTTTCCCTC[G/T]GTTCCCCCAGCAGAT | 58513 |
rs372804130 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418116 | GGCCCTGGGAGAAAC[A/G]TGGGGATGCTAATTA | 58513 |
rs372844915 | in-del | -/GGGT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412725 | GGGTGGGGGGGGGGG[-/GGGT]GTCAGAGGCCCTGGG | 58513 |
rs372851002 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376461 | CAAGGCTAGGAGACA[A/C/T]TGGCAGCACTGGCCA | 58513 |
rs372876215 | in-del | -/CTGT | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379857 | GTCACACAAAAGTGG[-/CTGT]CTAAGACTGTAGACT | 58513 |
rs372907109 | snp | C/G | 0.00208037 | 0.0321847 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441999 | GAAATGGGAGACCAA[C/G]AGGCAAAATAACTTT | 58513 |
rs372925875 | snp | A/G | 0.00148917 | 0.0272465 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386236 | AAGGGGTCGAGCTAA[A/G]TGAAAGGAGAGAGGA | 58513 |
rs372940566 | snp | A/G | 3.50042e-05 | 0.0041834 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402304 | CCCATACTGTAATAC[A/G]TTTATTCAACCTTTA | 58513 |
rs372974203 | snp | A/G | 6.60066e-05 | 0.00574447 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403724 | CAGGGACCCGACTCC[A/G]TGAAGTACCTGGTTG | 58513 |
rs372984824 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454230 | CTCCATGGGACAGAA[C/T]AAATACCTTACAGCC | 58513 |
rs372987523 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358689 | GATGGCCCCGGGAGG[C/T]GCCCGGCACCTGTCC | 58513 |
rs373006643 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401126 | GATGATGACGGGCCC[A/G]GGGGCGGCTATGGAA | 58513 |
rs373009906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389719 | ATGAAATTCACATGA[C/T]GGCTATAACATAAGA | 58513 |
rs373016755 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379839 | CTGAGGCTCCAGCAT[C/T]TAGTCACACAAAAGT | 58513 |
rs373018392 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432364 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 58513 |
rs373038454 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440250 | CCAGCCTGGCCAAGA[C/T]AGTGAAACACTATCT | 58513 |
rs373113510 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421597 | ATCAAACTCTCCTCA[A/C]TTCCATGAGCCAAGA | 58513 |
rs373122107 | snp | G/T | 3.30551e-05 | 0.00406528 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421471 | CACCACCCAGTTCAC[G/T]GTTGGCTGAAACAGT | 58513 |
rs373160332 | in-del | -/AAAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428518 | GAGAGAGAGAGAAAG[-/AAAG]TGAAAGAAAGAAAGG | 58513 |
rs373202621 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427073 | AGCAGTGGGAAGGGC[A/G]AGAGAGTGATGGAGG | 58513 |
rs373204716 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426537 | CCAGTTACTTGGAAG[A/T]CTGAGGCAGGAGAAT | 58513 |
rs373236225 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394789 | ACCTGCTGAGGGATT[A/C]GGAAACTGAAGTACT | 58513 |
rs373251077 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456913 | CAGGGTCTGTGCACG[C/T]TGTGCTGAAAAGACA | 58513 |
rs373253739 | in-del | CC/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461544 | GGAAAATCACTTGAA[CC/G]CAAGAGGCAAAGGTT | 58513 |
rs373306296 | in-del | -/GTGCGC | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472433 | TGTGTGTGTGTGTGT[-/GTGCGC]GCGCGCTAATTTGGG | 58513 |
rs373332509 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434550 | TGTGAATGTCCAGAC[C/T]GAGCTCTGACCGAAA | 58513 |
rs373363629 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455927 | TCCTGAAAGCCAGGC[A/G]CAGTGGATCACACCT | 58513 |
rs373373434 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411596 | ATTACATAGCCATCC[C/T]TCAGATTGGTATTAA | 58513 |
rs373403827 | in-del | -/ATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393078 | CTGCAGGAGCTGGAT[-/ATA]ATAATAATAATAATA | 58513 |
rs373460715 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377247 | GTGAAAGGGCCAGAA[A/G]GTGGGGGCTGTAAGA | 58513 |
rs373479180 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442278 | CCTTGGGGAAAAAAA[A/G]GGTTGCCCCCTCAAT | 58513 |
rs373534629 | snp | C/T | 1.65075e-05 | 0.00287289 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413833 | AATGTCTTGTTCCAG[C/T]GAATATTTCTCTCTG | 58513 |
rs373537238 | snp | A/C | 3.34666e-05 | 0.0040905 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361891 | CCCTTTTTACTTTGG[A/C]ACGGGTCGCCGCTGT | 58513 |
rs373544869 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394463 | TCGCCTCTCAGACCC[A/G]GCAGGCTTCAAACCC | 58513 |
rs373545811 | snp | A/G | 4.53176e-05 | 0.00475991 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428769 | TCCCAGACCTGCAAG[A/G]GAGAGACCAGCATGG | 58513 |
rs373660699 | snp | C/T | 0.000281977 | 0.0118705 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436907 | CTATCTGAAGGAGAG[C/T]CAAGGAGGGAGCTAT | 58513 |
rs373671774 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459649 | GGCCTGAGGATGCTG[G/T]TAAGTCCCAAATGAG | 58513 |
rs373675528 | snp | A/G | 0.000232199 | 0.0107725 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417539 | GTGGAGGGAAGGGCC[A/G]TTTCCAACATACCTT | 58513 |
rs373742235 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435395 | AGGGCAGGCAGCCCG[C/T]AAAAGGGGCCATGAG | 58513 |
rs373743903 | snp | A/G/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402422 | CGAGCACCTGGTCAT[A/G/T]CTGCTCCAGGCTCCT | 58513 |
rs373840006 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403685 | AGCCTCGGCTCTTGG[A/G]GCTCGCTGGTCCCTG | 58513 |
rs373866540 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358657 | CAGTTTAGACAGCTC[A/G]GCACGCTGGGCGATG | 58513 |
rs373883172 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356217 | GCTCTAAAGCCCCAC[A/G]GCGCAGACAATTCTG | 58513 |
rs373897585 | snp | G/T | 3.35081e-05 | 0.00409304 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361741 | AAGCTGCAAGCGGAA[G/T]GGAGTGGGGTGGCCC | 58513 |
rs373919380 | snp | A/G/T | 0.000117461 | 0.00766278 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421311 | AACTGCCACCTGTCC[A/G/T]GCCTTACCATATGTG | 58513 |
rs373934961 | snp | C/T | 3.35424e-05 | 0.00409513 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425036 | AACTCCCGAGAAACA[C/T]CCTACTGTGCTCTGA | 58513 |
rs373976968 | snp | A/T | 0.000187223 | 0.00967349 | missense, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361979 | GGCTTACAGGTGTAC[A/T]TTTACCTGGAAAGTT | 58513 |
rs374007572 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393694 | AAATAAATAAATAAA[A/T]TAAATAAATAAATTA | 58513 |
rs374028093 | in-del | -/CTAGACTGGA | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361206 | TTCAGAGTGGCTGTT[-/CTAGACTGGA]TTTCTTTTTTCATTG | 58513 |
rs374070120 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381794 | CTGTGGGTGCTTCTG[C/T]GATTCATGGAACATG | 58513 |
rs374082879 | snp | C/T | 0.000115305 | 0.00759205 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393994 | GGGGTCATTCTGGAA[C/T]GGGTCGCCTGGTTGG | 58513 |
rs374098048 | snp | A/G | 0.000164136 | 0.00905766 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425349 | AATGGCACTGAAGGG[A/G]CAAGGCTGGGGCCGG | 58513 |
rs374113216 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389135 | TTGAACTTGGGAGGC[A/G]GAGGTTGGAAAAAAA | 58513 |
rs374118834 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361192 | TTTTTGTTTTGGCTT[C/T]CAGAGTGGCTGTTCT | 58513 |
rs374256065 | in-del | -/AGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406295 | GAGGGCTGGATCTGG[-/AGGG]GACAATCAGGGTCAC | 58513 |
rs374282442 | snp | A/G | 4.85543e-05 | 0.00492695 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425278 | CAGGGCGGAGGGCAC[A/G]GGCTCCTTCTCCAGG | 58513 |
rs374287068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441495 | TTAGCCGGGTGTGGT[A/G]GCATGTGCCTGTAAT | 58513 |
rs374287732 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461626 | GACTCTGTCTCAAAA[A/G]AAAGAAAGAAAGAAA | 58513 |
rs374304767 | snp | A/C/G | 6.59114e-05 | 0.0057404 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392341 | TTCGTGAATGGATCC[A/C/G]AGGTAAATGGGTCAT | 58513 |
rs374310841 | snp | A/G | 0.000117929 | 0.00767794 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434501 | TCCACCTAGTTGGAA[A/G]GAAATAGCCCGAGTA | 58513 |
rs374317214 | in-del | -/ACAGA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428544 | AAGAAAGGAAGAAAG[-/ACAGA]AAAGAAAGGAAAAGA | 58513 |
rs374319426 | snp | G/T | 0.000117437 | 0.00766189 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417950 | CAGCACCACTCACCG[G/T]GCCGGGCGTGCCTCT | 58513 |
rs374324507 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465045 | AATTGCACCACTGCA[C/G]TCCAGCCTGGGCAAC | 58513 |
rs374353738 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434953 | TTTTTTTTTTTTTTT[-/C]TTTTTTTGAGACAAA | 58513 |
rs374383377 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377988 | TCCAGCTTAAAGAGA[A/G]AGACAGTCAGAGATA | 58513 |
rs374397831 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461033 | AGCTGGGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 58513 |
rs374470525 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400344 | TCCGTCTCAAAAAAA[A/C]AAAAACAAAAACAAA | 58513 |
rs374489341 | snp | A/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401701 | GCTCTCAAAAATGTA[A/C]GGGGCCGACAGTCCC | 58513 |
rs374504663 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447289 | CATCAGAGGTTTCTA[C/G]AGCAGAGCTAAGGTA | 58513 |
rs374620975 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435161 | TTCAACATGATGGCC[A/G]GGTTGGTCTTGAACT | 58513 |
rs374621128 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460207 | GACAGGAGGATGAAC[C/T]CAGGAGTCTGAGGCT | 58513 |
rs374621355 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398243 | AGGAGAATGCACCCA[C/T]ATCCCTGCCATCTGA | 58513 |
rs374624461 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376922 | CACAGGACGGGGCGA[C/G]GGCGGGCAGGCAGGA | 58513 |
rs374629221 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463365 | CACCTGTCCAAACAG[C/T]TACCCCACATATTCC | 58513 |
rs374690778 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378617 | CACAGTCCTCTCCCC[A/G]GCACCTGCTGCCTCC | 58513 |
rs374698700 | in-del | -/CCC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367773 | AAAAAAAAAAAAAAA[-/CCC]AAAAAACAACAAACA | 58513 |
rs374708374 | snp | A/C | 6.60731e-05 | 0.00574736 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377268 | GGCTGTAAGAGAGGA[A/C]ATGAAAGAGAGGCAA | 58513 |
rs374724590 | snp | C/T | 9.95999e-05 | 0.00705621 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417965 | GGCCGGGCGTGCCTC[C/T]CTCCGAAGGCGGGAC | 58513 |
rs374727521 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431705 | GAAGATTTGAATGTT[C/G]CCAACACAAAGAAAG | 58513 |
rs374736495 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428073 | GGGCATAGTGGCAGG[G/T]GCCTGTAATCCCAGC | 58513 |
rs374745864 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363099 | TCTGCTTGGTGACGG[A/G]AGGTCCCACCTGACG | 58513 |
rs374750013 | snp | A/G | 0.000478283 | 0.0154568 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413762 | GTAACCAAAACGAAC[A/G]AGACCCTTACCTGCA | 58513 |
rs374759343 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424576 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATCA | 58513 |
rs374833294 | snp | A/G | 6.61255e-05 | 0.00574964 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417614 | GCCAGTAAACTCCCC[A/G]GAGCCGAGAGAGCCT | 58513 |
rs374887016 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454574 | GGACCCAAATGAGTG[A/C]CTTGTGAGACCAGCA | 58513 |
rs374890324 | snp | C/G | 4.96003e-05 | 0.00497973 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437722 | ACATACACACACACA[C/G]ACATCTGGTATTAGA | 58513 |
rs374892503 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432026 | CAGGACTGATTGCAG[C/G]ACTTGAGTATGCGTA | 58513 |
rs374896016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468103 | CGGTCACAAAAGGGA[C/T]CCACGGAAGGTACAA | 58513 |
rs374909235 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449368 | CAGATGGCAAATAAA[C/T]GTATGAAAATATGTT | 58513 |
rs374911192 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359901 | GGGAAAAAAAAAAAA[-/C]AAAACAGAAAACAAC | 58513 |
rs374925692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371822 | CTAGAAACTCTTCAG[C/T]GGTGAGCTCTGACTG | 58513 |
rs374928439 | snp | C/T | 0.000214746 | 0.0103599 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385113 | GAGGCGCGGGGGCTC[C/T]GTGGAGGGGCTTTAC | 58513 |
rs374934623 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378804 | GAGGGAGAAAATCAC[C/T]TTCTATGGGCAGAAG | 58513 |
rs374940715 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412858 | GCTTGCAGAGGCAAG[A/G]CCGAGGATAAGGAGT | 58513 |
rs374946532 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455319 | TAAAGATTGGGGGGG[-/G]TCTCATTATTTTGCC | 58513 |
rs374974721 | snp | C/T | 3.295e-05 | 0.00405881 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394023 | GGAAGAGGAGAGAAA[C/T]GCTTATTAGCTCTAG | 58513 |
rs375023286 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372549 | AACGGAAAAGATTTC[C/T]ACTAAACTGTGACCT | 58513 |
rs375031066 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397282 | TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGG | 58513 |
rs375104276 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442242 | TGAAACCACAGATAT[C/T]GGTCAAAAGTGAACA | 58513 |
rs375161298 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386913 | CTCTTTGGAGAAAAC[A/T]GACTACAGTCTCTAC | 58513 |
rs375162718 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473560 | ACTACAGGGGACTGA[A/G]TATAAAAGTGTTGGA | 58513 |
rs375173945 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461160 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 58513 |
rs375185884 | snp | A/G/T | 0.000542592 | 0.0164627 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361758 | GAGTGGGGTGGCCCG[A/G/T]AGGCGGAGGACTCAA | 58513 |
rs375187631 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387737 | TGCCACTGCACTCCA[G/T]CCTGGGCGAAAGAGC | 58513 |
rs375194227 | snp | C/T | 1.65866e-05 | 0.00287976 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413726 | GAAGTTTTCCTGAAC[C/T]ACATTTAGCACAAAG | 58513 |
rs375195771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429961 | GGCCTTGACCCACCA[C/G]ATGCCAGCAGCACTC | 58513 |
rs375218299 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377750 | CCAGGTGCTGGGTCA[A/G]CTGGCACCAGACTTT | 58513 |
rs375232192 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438069 | TAAAATGGACTTATC[C/T]TGGCCAGGTGTGGTG | 58513 |
rs375249009 | snp | C/T | 0.000151665 | 0.00870685 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417508 | CAACCTGGGAGAGTT[C/T]GTGTAACATCTGGAT | 58513 |
rs375253035 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415708 | ACAGATGGGCACTCT[A/G]CACACACCAGCCTGT | 58513 |
rs375262792 | in-del | -/GC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375494 | TGTGTGTGTGTGTGT[-/GC]TTCTGCTCCCATCTT | 58513 |
rs375316286 | in-del | -/AAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366650 | AACATCAACAACAAC[-/AAC]GGTTTTTTTCTCAGT | 58513 |
rs375351441 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437710 | ATACACACATGCACA[C/T]ACACACACACACACA | 58513 |
rs375397101 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381777 | GAAAAACACTGGCCC[A/G]TCTGTGGGTGCTTCT | 58513 |
rs375434776 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450085 | AGACCCTATCTCTAC[-/A]AAAAAAAAAAAAATA | 58513 |
rs375464947 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359431 | TTTTAGACAATGATA[C/T]GACCCAAGGGGACAA | 58513 |
rs375513397 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455334 | GTCTCATTATTTTGC[C/T]AGGCTGGTCTTGAAC | 58513 |
rs375514446 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374733 | GGATGGCTCCTCCTC[A/G]GGGCCCAGCAAATAC | 58513 |
rs375532945 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450085 | AAGACCCTATCTCTA[A/C]AAAAAAAAAAAAATA | 58513 |
rs375540923 | in-del | -/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382899 | GTGCTTCAATTCAGG[-/G]ACTTACAAAAGGGCC | 58513 |
rs375544090 | snp | C/G | 0.000100329 | 0.00708199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434321 | GGCGCCCACACACAG[C/G]AGGGACACTGAGTGC | 58513 |
rs375546436 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403696 | TTGGGGCTCGCTGGT[A/C]CCTGGCATGTGGCAG | 58513 |
rs375559861 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383661 | TAAACACACACCCTG[-/C]CTCGGTCAGAAGTGG | 58513 |
rs375644909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420983 | GCACCTCCCGGAGGC[A/G]GCTGTGACAAAGTCC | 58513 |
rs375671112 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406875 | AAGATGATGGTATTA[A/G]GTGTGGGGCCTCTAG | 58513 |
rs375678729 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366741 | GCCGAGTGCCCGGTC[C/T]AGCTCTCGACCTTGC | 58513 |
rs375758505 | snp | C/T | 3.31846e-05 | 0.00407323 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418080 | TTTGCTTAACTTCCC[C/T]GTTTGCCTCGTATCG | 58513 |
rs375804390 | snp | G/T | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381913 | CCTTGTCCTCCCTGG[G/T]CATGTGCTGGCTTCT | 58513 |
rs375815375 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403726 | GGGACCCGACTCCGT[C/G]AAGTACCTGGTTGAT | 58513 |
rs375821912 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468402 | CCAGGCTGGGGTGCA[A/G]TGGCGCGATCTCAGC | 58513 |
rs375859725 | snp | A/G | 4.99463e-05 | 0.00499707 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425143 | GTTGAGGCTGCTGAC[A/G]CTGCCGTGGGACGGC | 58513 |
rs375870855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426605 | GATCATGCCACTGCA[C/T]ACCAGCCTAGATGAC | 58513 |
rs375882375 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383591 | CTCCGTGTGCTGGAA[A/G]GAGGGGGGCGCCATG | 58513 |
rs375929557 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472388 | CCCCGCAAAGCGCCC[C/T]GTTCCTAGGATCGCA | 58513 |
rs375957764 | snp | C/T | 0.000347939 | 0.0131852 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395292 | GAACCACTCTAAATT[C/T]GACATAAAACACACA | 58513 |
rs376001626 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430978 | AGTGGCTCACGACTG[A/T]CATCCATCCCAGCAC | 58513 |
rs376003951 | snp | A/G | 3.33639e-05 | 0.00408422 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425067 | GAGGGGGCTGTGCCC[A/G]CTGAGGGCTCCGTAC | 58513 |
rs376008025 | snp | A/T | 1.65386e-05 | 0.00287559 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395512 | ATTTTATTATTTCTG[A/T]GTTAAAGCAAAGTAC | 58513 |
rs376041404 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433272 | GTCTGGGATTACAGG[C/T]GAACACCACCACACC | 58513 |
rs376060955 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399277 | AAACGAGATTTCCCT[C/G]TTACAAAGATACCAT | 58513 |
rs376119323 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435280 | CCTCCATTTCTAATG[G/T]TAAATAAATTAATAC | 58513 |
rs376167338 | snp | C/T | 0.000139514 | 0.00835089 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377078 | TGGTCCCCCGCCATC[C/T]GGCACCGGTAGGCGG | 58513 |
rs376179332 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441588 | GAGCCGAGATCGCGC[C/G]GCTGCATTCCAGCCT | 58513 |
rs376199145 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422624 | ATGAACGCCATGATG[A/C]CTGAAACTGCCACTC | 58513 |
rs376199594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401479 | AGAGGGTGGCAGCAC[A/G]GAGAGAGCTGCTGGA | 58513 |
rs376207764 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465459 | AGGCAGAGGCAGGAG[G/T]ATCACTTGAGGTCAG | 58513 |
rs376221984 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380921 | AGATATGGCTGCCTC[A/G]GACCTTGTGTAGTCC | 58513 |
rs376223013 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446880 | CCATTTCCCCAGGAA[-/A]GCTGAGACCCCATAA | 58513 |
rs376223780 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459528 | GTGCAGTTGGTAGTG[A/G]GGAGCGGGCAGACAT | 58513 |
rs376236605 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359012 | CACGCAAATAACCCA[C/T]TGATGGAAATTTGGG | 58513 |
rs376272852 | snp | C/T | 1.72415e-05 | 0.00293606 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417921 | AAGGGATGTCAATAC[C/T]CCCAGGGCATGACCA | 58513 |
rs376322635 | snp | C/T | 3.34124e-05 | 0.00408719 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402337 | ATGGCTCCAAAACTG[C/T]CCCTCTCTGCCAGGG | 58513 |
rs376347457 | snp | A/G | 3.29897e-05 | 0.00406125 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437821 | CAAGGTAACTTCATG[A/G]CCACTCTGTGCACAG | 58513 |
rs376366550 | snp | A/C | 1.65446e-05 | 0.00287612 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403892 | CTGGGACTTTAAGTC[A/C]GATTCCTGAGATTGG | 58513 |
rs376373275 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461034 | GCTGGGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 58513 |
rs376401617 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421819 | AGGAAAGACCCTCCC[C/G]AGCACCCACTTGGAA | 58513 |
rs376405108 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403237 | AAGCCAGCGCCCCCC[C/G]CTGGACTGGGAAGAG | 58513 |
rs376419496 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379378 | TCAGAGTGGGGCAGA[A/G]GTGGAGGGAGGGGCC | 58513 |
rs376439335 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413613 | AGTGAATTCAGCCTG[-/A]AAAAAAAAAAAAACA | 58513 |
rs376453497 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464805 | TAAAAAATTCACGGG[C/T]GGGCATGGTGGCTCA | 58513 |
rs376476786 | snp | A/G | 2.27866e-05 | 0.00337532 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428772 | CAGACCTGCAAGGGA[A/G]AGACCAGCATGGGTA | 58513 |
rs376491057 | snp | G/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377196 | TGTTTACTTTTAAAG[G/T]GGTCATCTGAGAATC | 58513 |
rs376501101 | snp | C/G | 3.31713e-05 | 0.00407242 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437013 | TGCTGAGAAGAGAGA[C/G]AAACATTCCTTTGTG | 58513 |
rs376531008 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373482 | TTGGACTTTATGCTT[A/T]AAAAAAAAAAAAAAA | 58513 |
rs376558645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441451 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTGT | 58513 |
rs376565550 | snp | C/T | 9.92999e-05 | 0.00704557 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441970 | CACCCTCCCTGTGTA[C/T]GCCGGATCGACCTGA | 58513 |
rs376620925 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356269 | CTACCTCCAGCCATG[A/C/T]TCCAGAGAGCTCTGA | 58513 |
rs376648640 | snp | C/G | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403735 | CTCCGTGAAGTACCT[C/G]GTTGATTTCGTCTTG | 58513 |
rs376656826 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438427 | AAAATTTCAGATGCA[C/T]ATATTTTCCAAAAAC | 58513 |
rs376724947 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376686 | TGCCACCCTCACCCC[C/T]AACAGGCCCTCCCTG | 58513 |
rs376764014 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368980 | TATTCCACCCTCCCC[A/G]TCCTGCCAGAAAAAA | 58513 |
rs376769996 | in-del | -/GTC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444169 | GGGGAGAGGGAAAAA[-/GTC]AAAAAAAAAAAAAAG | 58513 |
rs376803810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452940 | TAGCTAGGACTACAG[A/G]TGCCCACCACCATGC | 58513 |
rs376835430 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378658 | TGAGCAGATACTAAG[C/T]GCCGCCACCTGGGGG | 58513 |
rs376847146 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404541 | GGAGTCCTTGGGAAG[C/T]CCCTGCCTGTGCATA | 58513 |
rs376874602 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458926 | GGTTAATTTCATCGT[C/T]GTGAGGACATCCTGG | 58513 |
rs376908068 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466645 | CGGTGCCTCCTGCCT[A/G]TAATCCCAGCACTTT | 58513 |
rs376940327 | snp | C/G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360801 | GTGCACGGTAGAGAT[C/G/T]ATCAAGACGGCTCAG | 58513 |
rs376967192 | in-del | -/GTGTGT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369676 | CTGGAAGAAAAAAAA[-/GTGTGT]GTGTGTGTGTGTGTG | 58513 |
rs376978041 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428250 | AGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 58513 |
rs376997080 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473830 | CGGTTGTGGTGGTGG[A/G]CACCTGTAATCCCAG | 58513 |
rs377019862 | in-del | -/TACAGGAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416852 | GGATCCAGAGGGGAA[-/TACAGGAA]GTGACTGCATTTCTT | 58513 |
rs377022207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358828 | CTTCAATAATTCGAA[C/G]CACGGCCTAGCTGAT | 58513 |
rs377039306 | snp | C/G | 1.66565e-05 | 0.00288583 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425152 | GCTGACGCTGCCGTG[C/G]GACGGCGTGGAGCGG | 58513 |
rs377042255 | snp | C/T | 4.94539e-05 | 0.00497238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394050 | CTAGGGCACAGGATG[C/T]GGGCCGGGCCCTTGG | 58513 |
rs377065517 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412454 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 58513 |
rs377088192 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355602 | CCCGAGTCCCGGTCC[C/T]TGGAGTACGGTGGCG | 58513 |
rs377089622 | snp | A/G | 5.05736e-05 | 0.00502834 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361874 | TAAACGGGTCCCCAA[A/G]CCCCTTTTTACTTTG | 58513 |
rs377090366 | snp | C/G/T | 5.097e-05 | 0.00504805 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425223 | CGGCGCCAGGGAACA[C/G/T]AGTCTTCTTTCTCTT | 58513 |
rs377091063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444013 | AGATTGCAGTGAGCC[C/G]AGATCGCGCCACTGC | 58513 |
rs377094496 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464850 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 58513 |
rs377099899 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399528 | CCCTTTAGAGGAGTG[C/T]TGGGCAGCAGGGGTG | 58513 |
rs377129788 | snp | A/C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371453 | ACTTAGGTAAAAGCT[A/C/G]TTCGTTAGTGCAACT | 58513 |
rs377182258 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395018 | TGAGGTCAAGAGTTC[A/G]AGACCAGACTGGGCA | 58513 |
rs377184653 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375443 | GTGTGCCAGCTGTGT[A/G]CATGCATTGTGATTA | 58513 |
rs377203990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460949 | TGGAGAGTGTGAAAT[A/G]AGATAGTTTTCTCTT | 58513 |
rs377217709 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376563 | GGGCAGAGGGGAGCC[C/G]CGAGCCATCCTGCCT | 58513 |
rs377237810 | in-del | A/GG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364762 | GTCCACTGGAGCAGA[A/GG]GGGGCTCCCTAGGGC | 58513 |
rs377300806 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413879 | TTCATGAAAACAAGA[A/G]TGAATAATAAGCCTC | 58513 |
rs377351934 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389922 | AATAAAAGGCCAATA[G/T]ACAGAATTCAAAAAA | 58513 |
rs377365202 | snp | C/T | 4.95103e-05 | 0.00497521 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385219 | AAAGGGATCTGCAAT[C/T]GGCACCAACAAAGTC | 58513 |
rs377366448 | snp | C/T | 1.67486e-05 | 0.00289379 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421313 | CTGCCACCTGTCCGG[C/T]CTTACCATATGTGTG | 58513 |
rs377379462 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386573 | TTCCGCCAGCTACAG[C/T]AGGAAGGCACAGTGA | 58513 |
rs377382575 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440262 | AGATAGTGAAACACT[A/C]TCTCTACTAAAAATA | 58513 |
rs377387004 | snp | G/T | 3.48699e-05 | 0.00417537 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361988 | GTGTACTTTTACCTG[G/T]AAAGTTTAGGAGAAA | 58513 |
rs377387815 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395967 | AAAAAAAAAATCAAG[G/T]TGTGGTGGCGTGTAC | 58513 |
rs377397670 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440960 | CCGATCACTGTCCAC[A/G]TGTTAACAAAAACCA | 58513 |
rs377417794 | snp | A/G | 1.65233e-05 | 0.00287426 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385109 | AGCAGAGGCGCGGGG[A/G]CTCCGTGGAGGGGCT | 58513 |
rs377456475 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364522 | GGCCCAGCCCGCAGA[A/C]CCCGGGCTGGTTCCG | 58513 |
rs377490596 | snp | C/T | 8.24858e-05 | 0.00642153 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417598 | CATCAAGCTCCTTCA[C/T]GCCAGTAAACTCCCC | 58513 |
rs377649713 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459739 | TACTCTTGTATTATT[A/G]TTCCTGAGACAGGGG | 58513 |
rs377654268 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381352 | GCTGGGGCCACCAGA[C/T]GCTGCCCTCAGCTGC | 58513 |
rs377693014 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400357 | AAAAAAAACAAAAAC[-/A]AAAAAAAAAAAAAAC | 58513 |
rs377700478 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464657 | AGGCTATTCCCCATG[A/G]CCTAGACCAGGGGTG | 58513 |
rs377737285 | snp | C/T | 7.74653e-05 | 0.00622308 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425257 | GGGTGGGATGAGGGA[C/T]GGGGGCAGGGCGGAG | 58513 |
rs377750293 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369454 | TTCCTGCCCTGTGAG[A/G]TGTGTGAGGTGGGCA | 58513 |
rs377756400 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403239 | GCCAGCGCCCCCCCC[-/T]GGACTGGGAAGAGGG | 58513 |
rs386807331 | multinucleotide-polymorphism | AGA/TGT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367986 | GAGAGAGAGAGAGAG[AGA/TGT]GTGTGTGTGTGTGTG | 58513 |
rs386807333 | in-del | CTTCCAGGTG/TACCAGCAAATACCAGAGCAAATACC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417462 | CCTGTGATGAGCAAA[lengthTooLong]AGCCTCTGATATTTC | 58513 |
rs386807334 | multinucleotide-polymorphism | ACA/TCT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430594 | AAATAAGTCTCAGCC[ACA/TCT]TAGCTATTACTTATT | 58513 |
rs386807335 | multinucleotide-polymorphism | ACG/CCA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432864 | CTGGAGTGCCATGGC[ACG/CCA]ATCTCAGCTTATTGC | 58513 |
rs386807336 | in-del | CTG/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439072 | TAGCTTGTTTTTTTT[CTG/GT]TTTTTTTTTTTTTTT | 58513 |
rs386807337 | multinucleotide-polymorphism | AT/GC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464810 | AATTCACGGGTGGGC[AT/GC]GGTGGCTCACGCCTG | 58513 |
rs397724212 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402726 | CAACAAACCAAGACC[-/C]CATCTCTGCAAAAAA | 58513 |
rs397823931 | in-del | -/C | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402727 | AACAAACCAAGACCC[-/C]ATCTCTGCAAAAAAT | 58513 |
rs397829760 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422423 | CTTCCCTTTTTTTTT[-/T]AAATATTTACACAAA | 58513 |
rs398034080 | in-del | -/A | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367526 | AAAAAAAAAAAAAAA[-/A]CTTGGTGGCCGGCTC | 58513 |
rs398034081 | in-del | -/GT | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369707 | TGTGTGTGTGTGTGT[-/GT]AGGGTGGGGTATGTG | 58513 |
rs398079756 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462324 | TACCACCAGGGCTGG[-/G]GTCCCGTTGCCACCT | 58513 |
rs527249301 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414101 | ACCTGGTTGCCCAAG[G/T]GGAAGTTAGAGATGT | 58513 |
rs527255382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445173 | ATGAGCAACAAGATC[C/T]GCAACCAAGAGAAAC | 58513 |
rs527258804 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380894 | ATCTGGGCTATTTGC[-/G]TCCCGTCACAGAGAT | 58513 |
rs527262944 | snp | A/G | 0.000336078 | 0.0129586 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355711 | GGCCCTCGCCTAGGC[A/G]GCAGGCATGTCAGCC | 58513 |
rs527275696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401017 | AGACGGAAACACACA[C/T]GCCAAGAACAGCCAG | 58513 |
rs527327228 | in-del | -/A | 0.0803491 | 0.183626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410748 | AGACCTTGTCGCTGC[-/A]AAAAAAAATTAAAAA | 58513 |
rs527330180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442833 | GATATTCCATTTCCC[A/G]ACACCTCAGAGCCCC | 58513 |
rs527379421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356413 | ACCTCCCAGGTTCAA[A/G]GGATTCTCTTGCCTC | 58513 |
rs527439484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368505 | CCACACAACTGTCAT[A/T]CACCCTACACAACAG | 58513 |
rs527478961 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358674 | CACGCTGGGCGATGG[C/G]ATGGCCCCGGGAGGC | 58513 |
rs527487663 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419710 | AGTCCGTGAACAGAG[A/C]TGCGGAGAATGAGCA | 58513 |
rs527490564 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389563 | GAAAACCAATCTTCA[G/T]TAACAAATGAAGAGT | 58513 |
rs527515302 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390156 | CAGTTTTAAAGATCC[A/T]GGTAAGTTGAAAGTA | 58513 |
rs527515971 | in-del | -/TTCACCTCCCAGG | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356395 | CGGCTCATTGCAACA[-/TTCACCTCCCAGG]TTCAAGGGATTCTCT | 58513 |
rs527549537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406726 | TCAAACCAAAGATGC[C/G]AAAATGTGTACATCA | 58513 |
rs527580289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451036 | GCTCACTACAACCTC[C/T]GCCTCCCAGGTTCAA | 58513 |
rs527580443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451667 | CCAAGTAGCTGAGAC[C/T]ACAGGTGCCCGCCAC | 58513 |
rs527595189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444352 | GCCCCAAGATGGCTG[C/T]CCCCCTCGTGCTTGG | 58513 |
rs527702690 | snp | C/T | 3.33973e-05 | 0.00408626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425064 | TGAGAGGGGGCTGTG[C/T]CCGCTGAGGGCTCCG | 58513 |
rs527772078 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380770 | TGCACAGACATGGCC[A/C/G]TTTAGGCCTCTGGAG | 58513 |
rs527793652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456597 | AGGAGGCTAGAGGTT[G/T]CAGTGAGCCAAGATG | 58513 |
rs527806656 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375466 | TGTGATTATGCATAT[A/G]TGTGTGTGTGTGTGT | 58513 |
rs527809324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381507 | AAGAGTGACAGAGCT[C/T]GGAAGGCTCCGGCAA | 58513 |
rs527812582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425662 | CCAGAAGAGAGACCT[A/G]TACTTCAAGACGTTC | 58513 |
rs527850043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443127 | AGCACACAAACCTGC[C/T]GCTGATGTAATAAGC | 58513 |
rs527865293 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451153 | ACCGGGTCTCACCAC[A/G]TTGGCCAGGCTGGTC | 58513 |
rs527956100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443747 | ATAATGCCCGGATTA[C/T]GGTCAGCGTCTCTGG | 58513 |
rs527956604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436649 | CCTAAAGATGCAAGA[C/T]TTAAACTGCAGCCCT | 58513 |
rs527957697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393033 | GGCAATAGAGTAAAA[C/T]CCCATCTCTAAATAA | 58513 |
rs527960658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439470 | GCCAAGATGGGAGGA[C/T]TGCTTGAGCACAGGA | 58513 |
rs527994003 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437557 | GTTCTGGAGCTAGAC[-/AG]AGGTAATGAAGACAC | 58513 |
rs528074300 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472706 | GCTTACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 58513 |
rs528087661 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370767 | GACCGTTCCTTGGCA[C/T]CGTCAGCAGGTCCCA | 58513 |
rs528095172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422481 | GCAATGAGAATAAAC[A/G]CCTGATTGAATTATC | 58513 |
rs528116988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465494 | TCGAAACCAGCCTGG[A/G]CAACATAGCAAGATC | 58513 |
rs528123374 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365255 | AACAAAGGGCTGTGT[C/T]CCCCCAACAATTGTT | 58513 |
rs528129076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459326 | CTTTGACAAGGGACA[C/T]TTCCTGAAGTTGATT | 58513 |
rs528140279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466058 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 58513 |
rs528182638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378195 | GATATGTGGCGACGT[C/G]TTGCAGGTAGGTAGG | 58513 |
rs528246150 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440653 | AAATAAATAAATAAA[A/T]AAATAAAAGATACAC | 58513 |
rs528256806 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404138 | ATGGGCTCATCCCAC[-/TG]TGGCTAACGGAAGAT | 58513 |
rs528266125 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357572 | CCAGATGGCAGGGCT[A/G]GGGGGACTGGGCAAG | 58513 |
rs528266962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402812 | CTGGTCTTGAACTCC[C/T]GGCCTCAAGTGATCC | 58513 |
rs528309474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396434 | GCCTGGCTAATTTTT[A/G]TATTTTTTGTAGAAA | 58513 |
rs528344290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389867 | ATGATATTTCCTAAA[G/T]CAACCTCTAAACAAT | 58513 |
rs528344778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391869 | ACGTGACTCTAAGGT[C/T]CCCACCAGTGCTGTG | 58513 |
rs528362242 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472946 | CACCACTGCACTCCA[A/G]CCTGGGTGACAGAGT | 58513 |
rs528362281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471874 | GCTCGCCTCGCGCCC[A/C]GCACCCCGGCGCCGC | 58513 |
rs528394325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390446 | CTCTCAGACACTGGT[A/C]GGACTAAAAAACAAA | 58513 |
rs528403506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383207 | GTCCTGGCCCGGCAC[C/G]GCCAATAGGAAGTGA | 58513 |
rs528416190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427975 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTAGGC | 58513 |
rs528433846 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434549 | GTGTGAATGTCCAGA[C/G]CGAGCTCTGACCGAA | 58513 |
rs528469563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414895 | TTTATTTTTTGTAGC[C/T]GAGGTCTCAATATAT | 58513 |
rs528472200 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408152 | CCTGGACCTCATTCC[A/G]TAATGGAGAAGGAGC | 58513 |
rs528490729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415789 | GGTGATTCACGCCCC[A/C]GCGTCCCTTCCTAGA | 58513 |
rs528501841 | snp | G/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472665 | AAATAAATAAGACAA[G/T]AACCCACTTGTTGCC | 58513 |
rs528511941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458903 | GCGTCCTGAGAGTTG[C/T]ATCGTCAGGTTAATT | 58513 |
rs528523953 | snp | C/T | 1.75517e-05 | 0.00296236 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402303 | CCCCATACTGTAATA[C/T]GTTTATTCAACCTTT | 58513 |
rs528531301 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452462 | GAAAAAAAAAAAAAA[A/C]CACAAGCCAGAGCCA | 58513 |
rs528532310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408669 | TCTCAAAAAAAAAAA[A/C]AAATCACATGGAAAC | 58513 |
rs528534452 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440410 | TGCACTCCAGCCTGG[G/T]CAACAGAGTGAGACT | 58513 |
rs528582140 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449000 | ATGGGCAAGCCAGGC[A/C]TGGTGGTGCGTACCT | 58513 |
rs528589172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446713 | ACAGGGCTGTGCACC[A/G]GACCACAGGACAGCC | 58513 |
rs528628048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364037 | TCTGGCCACCAGCTG[C/T]GGGAGATCCTTCCAG | 58513 |
rs528638971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394168 | TGCCCTCAAAACCTT[C/G]GCAAATCAAAGAGGG | 58513 |
rs528662051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470086 | ACAGGAAGAGGCTAA[A/G]AAGTCAGTGACCTGG | 58513 |
rs528712461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427077 | GTGGGAAGGGCGAGA[A/G]AGTGATGGAGGGAGG | 58513 |
rs528723842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464321 | CTGCACTCCATGCAG[A/G]AGCAAACTTCAGGGC | 58513 |
rs528764732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376447 | GGACCCTCGAGGGCC[A/C]AGGCTAGGAGACATT | 58513 |
rs528782676 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362922 | AACTCCAGGATGCCC[A/G]GTCCCAGCAAGGTAT | 58513 |
rs528802486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376914 | CAGGGGCCCACAGGA[C/T]GGGGCGAGGGCGGGC | 58513 |
rs528803916 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396820 | ACATGGAAGAACCTT[C/G]AGGAGAGGCTGCTGA | 58513 |
rs528810109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458512 | AGCCTCCTCACCCAC[A/G]GCCCTGCCTTCACCC | 58513 |
rs528810928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421121 | GACAGTGAACTGACC[A/G]TCACGGAGCGCGGGC | 58513 |
rs528842596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367516 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAACTTGG | 58513 |
rs528855637 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462144 | GACCAGTTGTTTTAC[C/G]TCTCTCCCTCTCAGT | 58513 |
rs528866319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405620 | CACAGCCCACACTGT[A/G]GGACGCTCCTTGGCC | 58513 |
rs528875760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412212 | GAGAAGCCACCGTCT[A/G]TGGTTATAAGCAACT | 58513 |
rs528889021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412898 | TCACCAAGCTGGGCC[A/G]CCTGGTCAAGGACAT | 58513 |
rs528910899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456452 | ACATGAGGTCAGGAG[C/T]TCGAGACCAGCCTGG | 58513 |
rs528925589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405975 | GAACTGCAGGGGCCT[C/T]GGGTGGGGTCCAGGG | 58513 |
rs528936898 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382480 | CTCTAAGAGAAACAC[A/G]TTTGAGTTCACCAGT | 58513 |
rs528946229 | in-del | -/TAATAATAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393118 | TAATAATAATAATAA[-/TAATAATAA]ACAACGCAGGTAAAT | 58513 |
rs528993964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443240 | AAAAGAGGACTATCT[C/T]GGGGGCAGGATTACA | 58513 |
rs528995671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360295 | ATAAATGAAGGGCTA[C/T]TCAAGAAACTCTAGA | 58513 |
rs529006248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443767 | AGCGTCTCTGGGGGA[C/T]GCCAACACCTGTGAA | 58513 |
rs529015133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360907 | TATAAATAACACATC[G/T]CACACCTAATGATGA | 58513 |
rs529056175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424050 | GCCTTGCCGTGGAGC[C/T]GGCTCTCCCAGTGAC | 58513 |
rs529060025 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410066 | TTGAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGC | 58513 |
rs529060341 | in-del | -/AAAC | 0.00835141 | 0.0640778 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388829 | AACTCTGTCTCAAAA[-/AAAC]AAACAAACAAACAAA | 58513 |
rs529096439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467733 | GGACAAGTAAGTGTC[C/T]GAGCCACTCAGCATT | 58513 |
rs529096771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417837 | GTTGAGGAAGGCAGG[A/G]ACCACAGGCAGCACC | 58513 |
rs529120918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385398 | TCTGGCATGGCAAGA[C/T]GGTTTCTCACTGTGA | 58513 |
rs529135565 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473242 | GATATTGAATACAGG[G/T]GATTGAGCCAGGCTC | 58513 |
rs529149060 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433436 | CGCACCAGGCTAAGA[C/G]TTTCTTTAAAGAGAA | 58513 |
rs529150619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408079 | GAAGATGGGAAGAGC[A/G]TTAGGCCGGATGGGG | 58513 |
rs529173397 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374866 | ATGAGCACACACGCA[C/T]GCATATGTGTGTGCA | 58513 |
rs529219907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359442 | GATACGACCCAAGGG[G/T]ACAAACAAAAACAAT | 58513 |
rs529220325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418534 | CATCTGAATGGCCCC[A/G]GCTACTGGCCTTCAA | 58513 |
rs529247260 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402967 | GTAATCCTACAGATA[C/T]TAACCATAAAGCACA | 58513 |
rs529286002 | snp | A/C/G | 0.00011535 | 0.0075936 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404702 | CTGTTTCTGAGCCTC[A/C/G]AGCTCCTGCAAACTG | 58513 |
rs529289603 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441701 | GTTTCTTATCTGCTA[A/C]CAAAGTAGTGGTGGG | 58513 |
rs529302929 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391833 | TGCACTTACTCCTGC[C/T]GTGACGGGAGCACCT | 58513 |
rs529355615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384895 | GGTCGTCAGACACCA[A/G]TGGGAGCCAGGGGAG | 58513 |
rs529376301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436020 | GCGCTGGGTGACAGG[A/G]AGAAACCCTTCACCA | 58513 |
rs529411901 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372731 | ATACAGCACGTCACC[A/G]TGCAAGGCGCTTCAC | 58513 |
rs529427726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364829 | CCTCCACCCTCCCGT[A/C]CCTAGAAGCCTCATC | 58513 |
rs529461342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423026 | ACCCGAAGATGTCCA[C/T]AGGATTGAGGAGAAG | 58513 |
rs529481408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417258 | CCACACAGCTGCCAC[A/G]GGCTCTGCCCACGAC | 58513 |
rs529498767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375538 | AAGAGGCCCACTGCC[A/G]TTCCATCAGGAAGCC | 58513 |
rs529541045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448380 | TACTAAAAATGTAAA[A/G]TTAGCCAGGCATGGT | 58513 |
rs529570347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441719 | AAGTAGTGGTGGGGG[C/T]TGCCACCTGGGCATT | 58513 |
rs529577352 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358931 | ATACACACATTTGCC[A/T]GAGACAGAAAGGCCT | 58513 |
rs529580727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404252 | GGTTGCAGCCTCCGG[G/T]ATCTGTGAGGAGCCT | 58513 |
rs529601344 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443291 | GGGACTGCTGTTGTA[C/T]GATTTCTCACAATGA | 58513 |
rs529615281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, missense | EPS15L1 | GRCh38.p7 | 19:16357008 | GATAACATGCGCAGT[G/T]GCTCTTCCCCAGGCA | 58513 |
rs529627774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439257 | TTGAGAAAAGGGGAC[C/G]TTTCATCCCTGCAAG | 58513 |
rs529681372 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416306 | CTGCATGGTGCCCCG[C/T]CATCACAAGAGTCCA | 58513 |
rs529700123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470736 | CAAGCATGCAACCGG[C/T]CTATCAACTCTCTTT | 58513 |
rs529703541 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461026 | AAAAGCCAGCTGGGG[C/T]CAGGCGCGGTGGCTC | 58513 |
rs529705071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394843 | AGCTGCCTTCAAATG[C/T]GGGTCTTGTGGTGAG | 58513 |
rs529721314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389014 | ATCACTTTGGGAGGA[C/T]GAGGCGGGCAGATCA | 58513 |
rs529731609 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388261 | GCCAGGCTGGTCTCG[A/T]ACTCCTGGCCTCAAG | 58513 |
rs529756693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382323 | TTGGGGACTCAACTC[C/T]TTCCTACTCGGGCAG | 58513 |
rs529761129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471534 | CGCCGGGACCGGAGG[A/G]AGACAAAGACTCGCT | 58513 |
rs529792792 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424586 | GAGGCCGAGGCAGGA[-/G]GATCACTTGAGCCAA | 58513 |
rs529800711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389506 | GAGCTATAAGAAGTG[C/G]TAAAGAAAGTTCTTT | 58513 |
rs529841511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433912 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC | 58513 |
rs529856557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407302 | TTTCTTCTCCCCACT[C/T]CCCAGCATTTTTTTT | 58513 |
rs529863761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427180 | TTCAAAAGAATTTTC[C/T]GTCGGAGGCCAAGGG | 58513 |
rs529870860 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451775 | ACCTCGTGATCCACC[A/C]GCCTCGGCCTGCCAG | 58513 |
rs529936620 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362125 | ACAGGCTGGACGGGG[G/T]TACCCTGGGGAATCC | 58513 |
rs529945306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362870 | GCTCCAAGGGGCAGC[A/G]TTTATCTGGGCCTTT | 58513 |
rs529946549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445896 | GATGTGTTCTCCTGA[C/T]CCAGCCCACTGTGCT | 58513 |
rs529971100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401403 | TATTCCAGGGAGGAA[A/G]AGGAATCCATGACGT | 58513 |
rs529993828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425702 | CCCAGCTACTTGGGA[C/G]GCTGAGGTGGGAGGA | 58513 |
rs530011124 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438512 | CATGGTTAAGGTTAC[A/G]AATGATGGACCAAAT | 58513 |
rs530038272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363328 | CTGCCTGTCCCTCCA[C/G]GGTTGACCTTGGATC | 58513 |
rs530150788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463676 | GCACAGTCTCTGCCC[C/T]TGTGGACCTAGTCTA | 58513 |
rs530153825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451137 | TATACTTTTAGTAGA[A/G]ACCGGGTCTCACCAC | 58513 |
rs530163948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381615 | CAATGATCACACCAA[A/G]TACGAAGCTGCGATT | 58513 |
rs530165105 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420511 | GATGACTCTGCGACA[A/G]CTAGTTCTCAGGCTC | 58513 |
rs530201726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381840 | CCCGTGCGAGTCCCC[C/T]GCGGCCTGGGATGGG | 58513 |
rs530203467 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465485 | GTCAGGAGTTCGAAA[C/T]CAGCCTGGGCAACAT | 58513 |
rs530235981 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468706 | GTTTTTGGAACAGGG[A/G]AATATGTTTTAGAAG | 58513 |
rs530239785 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421603 | CTCTCCTCACTTCCA[A/T]GAGCCAAGAGGGCAG | 58513 |
rs530240956 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376252 | GAGGCGTCCCAGACC[C/G]GGGCACAGATGGAAC | 58513 |
rs530271221 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366223 | AGCCGTTCCTGCAGG[G/T]AGTGATCACCTGAGG | 58513 |
rs530299524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393826 | ACAACATGGATGGAC[A/G]GCCGTCCTTCCCAGT | 58513 |
rs530314884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437703 | CATGCACATACACAC[A/G]TGCACATACACACAC | 58513 |
rs530327413 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355599 | GCCCCCGAGTCCCGG[C/T]CCTTGGAGTACGGTG | 58513 |
rs530347648 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393566 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 58513 |
rs530375545 | snp | A/G | 0.00210439 | 0.0323692 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425209 | AGGCAGGACGGGGAC[A/G]GCGCCAGGGAACACA | 58513 |
rs530376383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468574 | TGGTCTCGAGCTCCT[A/G]GCCTCAAGCAATCCA | 58513 |
rs530385825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423136 | AACAGGCTCCTGATA[C/G]CAACTCAGGGAAATC | 58513 |
rs530398360 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445733 | TCTGGAGCTGCCCAC[C/T]CATGTCTGACCCCAA | 58513 |
rs530402391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431562 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 58513 |
rs530503780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374524 | TTCTTTTCTGCTTTC[A/G]AAGCCCACAGTACAC | 58513 |
rs530516314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454357 | TATAAGCACACGGTA[C/T]CCTATCGCCCCGCTA | 58513 |
rs530547028 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427847 | TGCAGTGAACCAAGA[C/T]TGCACCACTGCACTC | 58513 |
rs530555963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417708 | GGAGGCACCAGCAGT[C/T]CTCGGGCCCAGGGAT | 58513 |
rs530592051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434593 | TGGCCACGGACCCAT[C/T]ATCACCCTTGGCTAA | 58513 |
rs530599735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373453 | AAAACATAAAGTCCA[C/G]CAGTTTGAAAACGTT | 58513 |
rs530611326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397159 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 58513 |
rs530616248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460711 | CCGCGGGCACAGAGC[A/G]TTCTAGTTCTCAGCA | 58513 |
rs530636874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454924 | CACCTGAGGTCAGCA[A/G]TTTGAGACCAGCCTG | 58513 |
rs530637128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374045 | AATGCTGCGCGTGCA[C/T]TGGCTGTTTTAGAGA | 58513 |
rs530648037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390515 | TCAACCTCACTGCCA[C/T]TTGTAGAGCATTACA | 58513 |
rs530675778 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399615 | TGTGGTGTAAACAGT[C/T]TCATCATGGTTGATT | 58513 |
rs530683323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383708 | AGGGCACGCACACAC[A/G]CGTCTTTGAAAACCT | 58513 |
rs530684879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391655 | GTTTTGAAATCCAAG[G/T]TGACACCTATTTAAC | 58513 |
rs530695711 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403233 | CGAGAAGCCAGCGCC[C/G]CCCCCTGGACTGGGA | 58513 |
rs530699452 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427875 | CTCCAGCCTGGGTGA[-/C]AGAGCAAGACTCCGT | 58513 |
rs530738029 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457871 | CCAAGACTGGGGGGG[-/A]AGGGGGGAACACCGA | 58513 |
rs530763866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364158 | GAAAGAGGGGAGGTC[A/G]AGGCCTGGTATCAGT | 58513 |
rs530771424 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472784 | CAGTATGGTGAAACA[A/T]CAATATGGTGAAACC | 58513 |
rs530808014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408800 | AGTCAGTGATGTAGT[A/G]GCATGAGGAGAGGCA | 58513 |
rs530811691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449382 | ACGTATGAAAATATG[C/T]TTAACATCATTAGCA | 58513 |
rs530818355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435164 | AACATGATGGCCGGG[C/T]TGGTCTTGAACTCCT | 58513 |
rs530839530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384343 | GAAGCACAATGGTGC[C/T]GCAGCCCTGTCCTTC | 58513 |
rs530846458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466145 | AGGCATGTGCCACCA[C/T]GCCTGGCTAATTTTT | 58513 |
rs530897934 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451979 | CTGTCTCTACTAAAA[A/G]TACAAAAAAATTAGC | 58513 |
rs530908918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357619 | ATGCAAGGAACCTGG[C/T]TGGGAGGCAGATGTG | 58513 |
rs530943424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409541 | ACACCATCAAGAATG[C/T]GGAAAGACAATCCAG | 58513 |
rs530959171 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366097 | AAATAGCAAGATTCT[A/G]GCAGAGGAAACAGTT | 58513 |
rs530966655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453432 | TTTAAAGGCCATTTG[C/G]GCTGGGCACAGTGGC | 58513 |
rs531001533 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422553 | GGCTGGAGGGATCGA[C/T]TGTTCCTTCTCCACG | 58513 |
rs531020081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447575 | GACCAGCCTGGCCAA[C/G]ATGATGAAACCCCAT | 58513 |
rs531043279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464970 | TGTAGTCCCAGCTAC[A/G]CAGGAGGCTGAGGCA | 58513 |
rs531049699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376949 | AGGAGGCACACACCA[C/T]GCACATACGGCACTT | 58513 |
rs531070753 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358243 | CCTTCAGAGTCGACC[A/C/G]GTTCAAGGCCAGCTC | 58513 |
rs531087583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421139 | ACGGAGCGCGGGCTT[C/T]GAGCCTTGGCACGTG | 58513 |
rs531089386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427829 | AACCCAGGAGGTGGA[A/G]GCTGCAGTGAACCAA | 58513 |
rs531106249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458927 | GTTAATTTCATCGTC[A/G]TGAGGACATCCTGGA | 58513 |
rs531124638 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371536 | TTAGGAGGTGAAAAG[C/G]TCATTAGCAGTAATA | 58513 |
rs531145045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415967 | TGGATAACACGGCCC[C/G]CAGGAGCTGAGACAG | 58513 |
rs531152797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421840 | CCACTTGGAAGGACC[A/G]TCCCTGGAGAACCGG | 58513 |
rs531157801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415110 | AAAAATTGATTATAG[G/T]TGTGAGCCACAAGGC | 58513 |
rs531165979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458592 | CTTCAGGGTGTGTAA[C/T]GGAGGCTAAGGTCCA | 58513 |
rs531168633 | in-del | -/CAGTGTTTGAGGTGATGGATATGCTAATTAC | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431724 | ACACAAAGAAAGGAT[lengthTooLong]CCTGCTGGGATGATT | 58513 |
rs531169655 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397218 | CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 58513 |
rs531174934 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450963 | GTACAGGCTCTTTTT[A/T]TTTTGAGACAAGAGT | 58513 |
rs531177190 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382905 | CAATTCAGGGACTTA[C/G]AAAAGGGCCTCCCTG | 58513 |
rs531178748 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423802 | CAGGGATCACAAAGA[-/G]GTAACAGGAGTCAGA | 58513 |
rs531250143 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368892 | GGTTTCTGAGAGTCA[C/T]GCTGCCTAGGAGAGC | 58513 |
rs531252640 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459215 | CCTATGCTTGGGGCC[A/G/T]CTGCCTGCTGCAGGC | 58513 |
rs531260989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400978 | GGGACAATGCCAGAT[A/G]GGGAAAGTAGGAGCC | 58513 |
rs531298038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443831 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 58513 |
rs531336607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406068 | GTTTGCGGGGAGCCA[C/T]GGCTGGGTGGTGGGG | 58513 |
rs531351019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400370 | ACAAAAAAAAAAAAA[A/C]ACCCCTGACTTTTGA | 58513 |
rs531364840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425000 | ATCACAAGCTTGACC[A/G]TTCTGGGGTTGCATG | 58513 |
rs531415038 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410389 | TGAGGCTGTGCAGAG[C/T]TGGCACCCTAGTACA | 58513 |
rs531425477 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354911 | TTAAGGATAAATTGT[C/T]TAAGGGGCTTATGGG | 58513 |
rs531436164 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462377 | GAATCAGGGAAGTGG[A/C/G]GGGGAGGGCATGGTG | 58513 |
rs531440474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374939 | CTGTATTCATGTATA[C/T]GTTCACATGTGAATA | 58513 |
rs531476000 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437981 | TCAACAATGAAGGCC[A/G]TCCGTGCAAAAACCC | 58513 |
rs531480118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375404 | TAAAAATACATGGCC[A/G]CACGTGGGAATGTGC | 58513 |
rs531488514 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387570 | CGAGATTATGCCATT[G/T]CACTGCAGCCTGGGC | 58513 |
rs531515376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368355 | ATGCACAAGCATCAT[C/T]GATCCTACACAACAG | 58513 |
rs531516054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457242 | TAGACACCTTGGTGC[A/G]GGTGTGGAGGTGAAC | 58513 |
rs531524154 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356286 | CCAGAGAGCTCTGAG[A/G]CCCTCTGAGGGTCAT | 58513 |
rs531531375 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467066 | AGGGCAGTGAAGGAA[-/T]ATCTGGGAATCCAAA | 58513 |
rs531560346 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419270 | TCGAGACCAGCTTGG[A/C]CAACATGGGGAAATC | 58513 |
rs531579009 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413442 | TCTAAGACCTACAGC[G/T]ACCTGACTCCCAACC | 58513 |
rs531630469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456563 | TTGGGAGGCTGAGGC[A/G]GGAGAACCGCTTGAA | 58513 |
rs531650653 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467799 | GAGGTGCCCAGCAGG[A/C/T]CATCTGGAACAGCAG | 58513 |
rs531670633 | in-del | -/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448601 | GTAATCCCAGCACAT[-/TG]GGAGGCCAAGGTAGG | 58513 |
rs531673590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412951 | AGCTATCTCTTCTCC[C/T]GCCCATCAAGGAATC | 58513 |
rs531688311 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365182 | CTGGGGCTGGGAGTG[A/G]CCCTGGAAGACGGTG | 58513 |
rs531712109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468373 | TTTTTTGAGACTGAG[A/T]CTCACCCTGTTGCCC | 58513 |
rs531712333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461579 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 58513 |
rs531717728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386118 | TTAACTGCGGGGGAG[A/C]TCTGCTACTGCCCAA | 58513 |
rs531727620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399703 | TTTTTTTTTTAGAGA[C/T]TGAGTCTCGCTGTGT | 58513 |
rs531765957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392997 | CAGTGAGCTATAATT[A/G]CGCCACTGCACTCCA | 58513 |
rs531767663 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469079 | GAGGGAGTGGGCAAG[C/T]AGGAAGTAGAATGGC | 58513 |
rs531791982 | in-del | -/AAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449276 | AACAAACAAACAAAC[-/AAAA]AAACACGAAGAAGAA | 58513 |
rs531798831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385522 | TGGGTCAGGAGGCGA[A/G]GAGCAACTCCAGGGC | 58513 |
rs531812856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456394 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 58513 |
rs531839906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380116 | TACACAGATGCGGCC[A/G]TCTAAGGCTCCGGCA | 58513 |
rs531883113 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405478 | CCGAGGCTCCAATGC[A/C]CCATGATTCCACTTC | 58513 |
rs531894131 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366436 | TGGGAGGAGCGGTTA[A/C]GAATTCTGCCTGCTA | 58513 |
rs531922667 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459477 | GGGTGAGATTAAAGT[A/G]TTGAGGGAGGCAGGT | 58513 |
rs531924182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436056 | ATTGCCACTGGCAAA[C/G]TGCTTGATGACAGAG | 58513 |
rs531924301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443076 | GGCTGTAAAAGTTTA[C/T]GTGCGTTGGTGTTTT | 58513 |
rs531930842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411363 | TTAATGGAAAGTTAG[C/T]GTCAAACTCTTCCAC | 58513 |
rs531936601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433930 | ATCGTGCCACTGCAC[C/T]CCAGCCTAGGCAACA | 58513 |
rs531943667 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404959 | CACCAGCTCCCTCAG[C/G]AGGTATTTCCCGATG | 58513 |
rs531951997 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446224 | AACCCAGCAGAACCA[C/T]CTCGGAGGAGAAACT | 58513 |
rs531995856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398737 | ATCCCACTACTGAGC[A/G]GCGTGGGAGTTTTGA | 58513 |
rs532022916 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393806 | GAACGGGACCGAGAA[C/T]GGGTACAACATGGAT | 58513 |
rs532024393 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462915 | CTCCTGTCCTTTATT[C/T]CCAGCCCAGTGGAGG | 58513 |
rs532058446 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471668 | GGTCCGGGCCCTGGG[A/C]GGAGAGGACACGCGC | 58513 |
rs532102015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458982 | CAGCGCCTGCTCCAC[A/G]CCTGGGCTGTGGTCT | 58513 |
rs532111139 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377585 | CCAGGACTTGGCACA[C/T]AGGGTCCCTTGGGCC | 58513 |
rs532133358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421920 | GGCTGCCCTACAGGC[A/T]GCCAAAGTGTCCTGT | 58513 |
rs532134751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389087 | GGTGAAACTCCATCT[A/G]CATTAAAAATACAAA | 58513 |
rs532174320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446110 | GGGGCACAAGGAGAA[A/G]GACAAGTTCACATCC | 58513 |
rs532193555 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472635 | CAGAAGCGAAACTCT[G/T]TCTCAAAAATAAATA | 58513 |
rs532206086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408085 | GGGAAGAGCGTTAGG[A/C]CGGATGGGGTAGCTC | 58513 |
rs532235469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383601 | TGGAAGGAGGGGGGC[A/G]CCATGCCAGGGCCTC | 58513 |
rs532257572 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452228 | AGGTGGGTAGATCAC[C/T]TGAGGTCAGGAGTTC | 58513 |
rs532258257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465347 | ATTCTGCATGGGCCA[A/G]GAGCACTGATTACCA | 58513 |
rs532264030 | snp | A/G | 0.00762888 | 0.0612882 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428577 | GAAAGGAAAAGGAAA[A/G]GAAAAGAAAAGAAAA | 58513 |
rs532295040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357112 | CCTGCAGACTAACCC[A/G]GGAAGGTGGGGGAAA | 58513 |
rs532295638 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464894 | ACCATCCTGCCTAAC[-/A]CAGTGAAACCCCGTC | 58513 |
rs532298213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363392 | CAGCCACACCTGCCC[C/T]GCCCACCACCTGAGC | 58513 |
rs532361882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420595 | CAAGCCACTAAGTAA[C/T]ATCCTGAATTTCACT | 58513 |
rs532444946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376380 | CGCCGGCCTAACTCT[C/G]TCATACGAGAGAAAT | 58513 |
rs532479234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369371 | AGGGAACAGGATGAG[A/G]TTTGGTTCTGAACTG | 58513 |
rs532505882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414778 | GCAGTGGCACGATCA[C/T]AGCTCACTGCATCCT | 58513 |
rs532584748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457968 | CACTTCCCAGAGTCT[C/G]CCAACTTTCCAAAGT | 58513 |
rs532593659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387473 | TTAGATGGGCGTGGT[A/G]GTGGATGCCTGTAAT | 58513 |
rs532595760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394447 | TCAGGGGCTGCCAGA[G/T]TCGCCTCTCAGACCC | 58513 |
rs532613336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432623 | ATACAAATACAAAAA[A/T]TAGCCGGCTGTTGTG | 58513 |
rs532618926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376758 | GGCCACAGGGCTGCC[A/G]GCCATGAGTGGCTCC | 58513 |
rs532632509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369933 | GCATGAGCCAGGCAC[A/G]GGGAGCCCTGACAGG | 58513 |
rs532656993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469962 | CACCTGGGCCAACAG[G/T]AACCCATGGTGTAGA | 58513 |
rs532665969 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370412 | GTGCCAAGCAAGGGG[C/T]TGAGGTGTCCTGGAG | 58513 |
rs532670451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362974 | AGAAGTGTTCAGAAA[C/T]GGAGGAAAATGACAC | 58513 |
rs532672602 | in-del | -/TTTTTG | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433123 | CTAAATTGAGGGTTT[-/TTTTTG]TTTTTGTTTTTGTTT | 58513 |
rs532694246 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432200 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 58513 |
rs532755127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425854 | GAACTGAGGATGCAT[C/T]CATGAGGCAGGCCAC | 58513 |
rs532790263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418408 | TGCAGCTGCCTCTTC[C/T]TTTGGCTTATCTCGT | 58513 |
rs532805096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381629 | AGTACGAAGCTGCGA[C/T]TGGAATCTGGGAGTG | 58513 |
rs532828544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412133 | TTTTAATCTGTGGTT[C/G]GTTAGATCCAAAGAT | 58513 |
rs532852597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405141 | ACTACAGTCACACCT[C/T]GTGGGCAGGGAAGAT | 58513 |
rs532861327 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365709 | CAGCTTCTCCCTCCA[C/T]GGGAAAGCCCCCCCT | 58513 |
rs532866310 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374822 | TGTGTACACGTATGT[A/G/T]AGCACAGAGTGTGCA | 58513 |
rs532873900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449167 | TAGTCCCAGCTACTC[A/G]GGAAGCCAAAGCAGG | 58513 |
rs532878914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464197 | ATGGAAATCCGAGAC[A/G]AATGTCTGTGGTCAT | 58513 |
rs532926458 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458593 | TTCAGGGTGTGTAAC[G/T]GAGGCTAAGGTCCAA | 58513 |
rs532980441 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418549 | GGCTACTGGCCTTCA[A/G]TGGGGATGACAGCAG | 58513 |
rs532984392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374329 | GCAGAGCACCGAGTG[A/G]CACAGCAACCATCAA | 58513 |
rs532994844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461497 | TGTGGTGGCATACAC[A/G]TGTGGTCCCAGCTAC | 58513 |
rs532994898 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455088 | GAGCCAGGATCACAT[A/C]ATTGCACTCCAGCCT | 58513 |
rs533005398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384453 | TGTTTTTTGACTTGT[C/G]CATTCTGGATGTTCC | 58513 |
rs533019723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466265 | GATCTGCCCCTCTTG[C/T]CCCTATACACTGAAG | 58513 |
rs533022558 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384856 | ACTCGGCCATGGCAA[A/T]GACTTCACCGTCTGA | 58513 |
rs533047801 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449705 | CTGTATGCAGTGTTG[C/G]CCACAGCTTTATATG | 58513 |
rs533058912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455675 | CTGCTGGAATGCTGT[G/T]CAACCCTGGGGCAGG | 58513 |
rs533095227 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407173 | CACATGCCATGTCAG[C/T]GTCTGCAGTGACAAA | 58513 |
rs533109688 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405549 | ATACAACGTCTATGA[C/T]AGCAAAATCCGTAAA | 58513 |
rs533118594 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437379 | ATGCTGAGAGAGAGG[-/C]CCAGACACAAAAGAC | 58513 |
rs533129390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358291 | ACTTGCATTGGTGAG[A/G]TCTGTATGCACTTAG | 58513 |
rs533181244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429774 | CTCCACAGACTCCAC[A/G]GGGACCTCCACCTAC | 58513 |
rs533197946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432365 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTG | 58513 |
rs533214349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466818 | TGAGACAGGAGAATC[A/G]CTTGAATCCAGGAGG | 58513 |
rs533217310 | in-del | -/GGAGGCTGAGGTGGGT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422716 | AATCCCAGCACTTTG[-/GGAGGCTGAGGTGGGT]GGATCACCTGAGGCC | 58513 |
rs533258346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379530 | GGAAAAGGTCTACCA[C/G]CACGTCCAGCAGACA | 58513 |
rs533317303 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424298 | TGATCCTACCAATGC[C/T]GTCGTGGGGGCAGGA | 58513 |
rs533325327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448257 | CATGTAAGGCCTGGC[A/G]TGGTGGTTCATGCCT | 58513 |
rs533341745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410128 | AACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 58513 |
rs533389774 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371627 | CTGGCTGGTGTCACC[A/G]GGCGCTGCAGGCAGG | 58513 |
rs533402410 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402701 | TGCGTGTCACCACCT[A/G]TATTTTTGGGCAACA | 58513 |
rs533426768 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372524 | GTTCAACTCCCTGCA[C/T]GCTTTTTTTAACGGA | 58513 |
rs533444395 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401153 | GGAAACCACCTCATT[A/G]CGAGTCCACGAGAAA | 58513 |
rs533455455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454094 | GGGAGACTGAGAAGT[A/G]ATGCAGGAGTGGGGG | 58513 |
rs533456659 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453574 | AAAAATTAGCCCAGC[A/G]TGGTGGCAGGCGCCT | 58513 |
rs533457695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358886 | ACTTCCAAAAGAACC[A/G]TTCCGCTAACCTAGA | 58513 |
rs533486701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400230 | TAATCTCTGCTACTC[A/G]GGAGGCTGAGGCAGG | 58513 |
rs533496489 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404906 | CACACCCACGGCCAA[A/T]GTGTGCCTCTTGGGC | 58513 |
rs533503922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435254 | ACCAAGCCCAGCCAC[A/C]TACAGGAAGCCCTCC | 58513 |
rs533522123 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371855 | CTTGATCTCCGGTCC[A/G]TTGCAGAAAATATAC | 58513 |
rs533549577 | snp | A/T | 0.029116 | 0.117091 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393659 | GTCTCAAAAAAAAAA[A/T]AAATAAAAAATAAAT | 58513 |
rs533556538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416036 | GCCTGACTCAGGCCG[C/T]GGCTCAGGTTTTCTA | 58513 |
rs533562012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422357 | CCTTCAATACACCCA[C/T]CACGCCACAGTTCAC | 58513 |
rs533566659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416739 | TAGGAAACAGATGCT[A/G]CAGTGAGCCATGATC | 58513 |
rs533612693 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387601 | AACAAGAGTGAAACT[C/G]CGTTTGAAAAATAAA | 58513 |
rs533617673 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378156 | TAGAGACAGGGAGGC[A/G]GGTGGGTGGTAGACA | 58513 |
rs533619524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469462 | CACGGAAGGCTTTTT[A/G]GAAAGCAGAAGAGAG | 58513 |
rs533630521 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409685 | GCTCCCGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 58513 |
rs533633700 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446173 | CACACAAGCGCCTGT[A/T]ACTGTAACCCAGGAC | 58513 |
rs533698695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360588 | CTCTACAAAAAAAAA[A/C]AATTAAACATTAGCC | 58513 |
rs533742516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431702 | AGAGAAGATTTGAAT[A/G]TTCCCAACACAAAGA | 58513 |
rs533787986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468878 | TTAATTAGCTGGGTA[G/T]GATTGGTGCTGCGCT | 58513 |
rs533833415 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442764 | AGAGCGCTGGCCAGT[A/C]ACTGTTCCCACCAGG | 58513 |
rs533844334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443892 | ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 58513 |
rs533899135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375670 | AAATGTCTTTGATGT[A/G]TGGCTTACAGAAATG | 58513 |
rs533907624 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391623 | ATCACCGAGGCTGCT[-/T]TTTTTTTTTTTTTTT | 58513 |
rs533922200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425992 | TTGCCAGATTAAGGC[A/G]AGACTCATCAGCGAT | 58513 |
rs533944033 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430907 | GGATCATAGGGATGC[A/G]GAGGGACATGGGTGC | 58513 |
rs533978272 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461654 | AAAGAAAGAAAAGCC[A/T]GTTTTCTACAGATTG | 58513 |
rs533982609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455976 | GAGACCAAGACGGGT[A/G]GATCACCTGAGGTCA | 58513 |
rs534018747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375002 | TAAGCATGGAGGGTG[C/T]GCATGCCCAGCTGTT | 58513 |
rs534027120 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461177 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 58513 |
rs534030563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443549 | ACACCATCTCTACAA[A/C]AAATACAAAAATTAG | 58513 |
rs534051810 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393453 | AAGAGTGTGAGACGA[G/T]CCTGGCTAACACGGT | 58513 |
rs534076601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452502 | GCACTCGCCTGTAGT[C/T]CCAGCTACTCGAGAA | 58513 |
rs534091024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436096 | TGACTCCTCAGTCAC[A/C]TGACATATCTTCATG | 58513 |
rs534092898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429609 | GCTGGCCTCCCTATC[A/C]CAGTCTTGTCCCTAT | 58513 |
rs534127934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398775 | CGCTTCTGACCAGGG[C/G]AGGTTTACCTCTCCT | 58513 |
rs534131861 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463388 | CATATTCCTTTCACC[A/C]CCAGCCCTTTCTACT | 58513 |
rs534137793 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433741 | GGAGGCCGAGGCGGG[G/T]GAATCTGAGATAGGA | 58513 |
rs534242106 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391504 | GAGCCCTGAGAAGGA[-/G]GGGTGAGTGCCCGTC | 58513 |
rs534302864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458702 | CTCACACACACTCAG[C/T]CACACACACATACAC | 58513 |
rs534318975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412369 | GCCAGGCATGGTGGT[A/G]CGTGCCTGTAATCCC | 58513 |
rs534365215 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373888 | GCTGCAAGCTCAAAC[A/G]GCAACCACCACACGG | 58513 |
rs534370342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453114 | CTTTATTTTATTTTT[C/T]ATAGAGACAGAGACT | 58513 |
rs534388263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391954 | TGATTTAGTCTTTTT[G/T]GGGAGATGAAGGGGC | 58513 |
rs534403749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449924 | CATACTGAATAATTC[C/T]ATCACATAACATCAT | 58513 |
rs534404723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363686 | AGGGCGCCAAACAAG[A/G]TGACATTCCTGGGGT | 58513 |
rs534431357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384735 | TTCTGTCACATGGGC[A/G]ACTCTGAACACTCGC | 58513 |
rs534441681 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391100 | GTAAATTGAACCATC[C/G]TAAGTCAGGGACCGC | 58513 |
rs534441729 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447339 | GAAGACTTGGCAAGT[A/G]AAAAGAGAGCTTTTC | 58513 |
rs534469126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384973 | ACTGCAGTGCATTGG[A/G]TCACAGCCATGGATG | 58513 |
rs534483953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433411 | TGCTGGGATTACGGG[C/T]GTGAGCCACCGCACC | 58513 |
rs534569982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422020 | TGTGAGTACACACAC[A/G]TCACTGACAGGTAAC | 58513 |
rs534587824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427352 | TGCCTGGGACCACAG[C/G]GTTTCAGTTCTGGAG | 58513 |
rs534592663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465036 | GTGAGCCGAAATTGC[A/G]CCACTGCACTCCAGC | 58513 |
rs534654523 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377638 | CGCCCCACCCTCACC[C/T]GTATGCTGGCTGTGG | 58513 |
rs534680932 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415044 | TAGAATTCGTGCATG[C/T]ATTTCCTAGCACTGC | 58513 |
rs534704031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371662 | GCAACGCAGGGCCGC[A/G]CTGGCAGGAAGTGGC | 58513 |
rs534715701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401577 | AAGACGAAATGGGAA[A/G]CTACATGTCCCCAGG | 58513 |
rs534740521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409042 | GCCTGAGCAATACAG[C/T]GAGACCCTGTCTCTT | 58513 |
rs534742881 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430917 | GATGCGGAGGGACAT[A/G]GGTGCATAGATGCAT | 58513 |
rs534804248 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433040 | GGACTCAAACTCCTG[A/G]ACTCAAGTAATCTGC | 58513 |
rs534847704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382130 | TCGGGCCAAGCCGGC[G/T]TGGCGCCTCCCATGT | 58513 |
rs534850343 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360063 | CCTTGAAACCTTGGG[G/T]GTTTTTTTTTTTTTT | 58513 |
rs534853255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389118 | AATTAACCAGAAATC[A/G]CTTGAACTTGGGAGG | 58513 |
rs534864971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420015 | CCTGCTCTGCTGACC[C/T]GTACGGTGGCAGCCA | 58513 |
rs534884810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463846 | ATGCCCCAGCTGATA[C/T]GAAAAGGTGTAGGGA | 58513 |
rs534885627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382635 | GGCTTTTTTTTTTTT[C/T]CAGGGCAGAAGAGGG | 58513 |
rs534899233 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367413 | CAGTTTCAACAGTTA[A/C]CCAAGCGGTGTACCG | 58513 |
rs534927969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377067 | CAGGGAGGCCCTGGT[C/T]CCCCGCCATCCGGCA | 58513 |
rs534935675 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357241 | GCTGGGGACACTGAG[A/G]CCAGGGAAGGGGTGG | 58513 |
rs534956922 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376020 | ACACAGGGGCTGCAA[A/G]GTGAGGCCAGTGGCA | 58513 |
rs534974916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363105 | TGGTGACGGGAGGTC[A/C]CACCTGACGGGCCTT | 58513 |
rs534975149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356089 | GTGTGACCTTAACCA[C/T]GACCTCTGGGCCTCA | 58513 |
rs534999504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401187 | GAGTATGGGAGGAAA[A/G]AGGGAGGCGGTGCAC | 58513 |
rs535015865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407029 | AGTGGGTCCTCACCA[A/G]ACGCTGAATCTGCAG | 58513 |
rs535077846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405274 | GGGTCGGGGGGTGTC[A/G]CACTCCAGCTAGAGC | 58513 |
rs535104586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417144 | TGCCACAGGCTCTGC[C/T]CATGACCTGCCTGGG | 58513 |
rs535184047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430321 | AGGTGAAGAGGGCAG[G/T]CTCTAGGGACAGCTG | 58513 |
rs535270269 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392294 | CCGGGCAACGTCCCA[C/T]CCCACTCACCTTCGA | 58513 |
rs535273942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457648 | TGGCGCCCGGGCAGG[A/G]GGGGAACAGATTCCA | 58513 |
rs535288403 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457998 | TGTACCCCGGGCCTT[A/C]CCAACATTCCTTTCC | 58513 |
rs535295119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451340 | GGAAACCTAATGACC[A/G]AATGCAAGGTGACAT | 58513 |
rs535343952 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455394 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 58513 |
rs535351414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444788 | CTGGAGAGCAGTGGC[A/G]CAATCTCAGCTCATT | 58513 |
rs535359526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362441 | GAATTAGTTTCACAA[A/C]GTGGTATGGTTATTC | 58513 |
rs535393089 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404453 | TGGACACTTTTCCAC[A/G]TGGTGTTTGGAGGAA | 58513 |
rs535393334 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403625 | CTCCCAAAAGAGACC[C/T]TCACGTAAGTAACAA | 58513 |
rs535403039 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433501 | GAAAATACTTTTACC[G/T]TGAGCTTTATCAGAA | 58513 |
rs535404238 | snp | C/T | 6.87214e-05 | 0.0058614 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441875 | CAGAAGAGAAATCAC[C/T]ATTCATCTTCACATA | 58513 |
rs535409705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366655 | CAACAACAACAACGG[G/T]TTTTTTCTCAGTTGT | 58513 |
rs535416038 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411512 | CTCGATAGAGTGATG[A/G]TTAATCAACACGGTG | 58513 |
rs535443133 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369643 | ACATAAAACCTGCCA[A/G]GCAAGGGCTGCACCA | 58513 |
rs535446152 | in-del | -/AAGA | 0.41833 | 0.184838 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428536 | TGAAAGAAAGAAAGG[-/AAGA]AAGAAAGACAGAAAA | 58513 |
rs535459669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473811 | TAAAAATACAAAAAT[C/T]AGCCGGTTGTGGTGG | 58513 |
rs535467995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442636 | TCATAAATCACCAGG[A/C]CTGCAAGCTTTCGAC | 58513 |
rs535490204 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384082 | GAGGGGGGCTGTGTT[C/G]TGCTTGTGGCTACTG | 58513 |
rs535506443 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385479 | AGTTGCCACAGAGGC[A/G]TGGCCCCTGGGTCCC | 58513 |
rs535527993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378498 | CTGCCGTCCCCCAGA[C/G]CTCTCCCAGGGCTCT | 58513 |
rs535546271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459552 | CAGACATAGCTCTGT[A/G]GCTCAGTAGCAGTGA | 58513 |
rs535588539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372953 | GTCCTGGCCTCACAC[A/G]TCAGCCATTTCCTGG | 58513 |
rs535613585 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357794 | GCTAAACACTTGGGG[A/G]TCTGATGAGTCTCCA | 58513 |
rs535619669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417033 | CCATCTGAGACCCAA[C/T]TGCCCTAGCTGTCAA | 58513 |
rs535660380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410507 | CTCCCAGGTATACAC[C/T]TGAGATAAAGGCAAA | 58513 |
rs535686692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447737 | TGCACTCCAGCCTGA[A/G]CGACAGAGCAAGACT | 58513 |
rs535687752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373642 | ATAACCAGAGGCCTC[C/T]TGGGCTGCACGTGGG | 58513 |
rs535688785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396743 | TCAAGAAAATTGTAA[C/T]GAGCCACACAACAGA | 58513 |
rs535691244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454466 | TTCCCTGGTGTACTA[C/T]GTCAGCATGAGCTGC | 58513 |
rs535702931 | snp | A/T | 0.00013238 | 0.00813465 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440770 | GCCTAGTAATACTTG[A/T]CAGTGGAGGAATGTG | 58513 |
rs535703542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455121 | GCAACAAGAGCGAAA[C/T]TCCATCTCAAAAAAA | 58513 |
rs535744430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358432 | TCTGGGTGGGTCACA[C/T]GGGCCAGAATCTGGA | 58513 |
rs535763889 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458658 | ATCTCCTACCTTGCC[A/G]GGCTGATTTCACTCC | 58513 |
rs535768063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434303 | ATGGGGAAAGAGAAC[A/C]GTGGCGCCCACACAC | 58513 |
rs535769599 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449279 | AAACAAACAAACAAA[A/C]AAACACGAAGAAGAA | 58513 |
rs535771864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359100 | GGTGCGGGTGACCTG[A/G]GCCCCCCTGACTGCC | 58513 |
rs535864304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387745 | CACTCCAGCCTGGGC[A/G]AAAGAGCGAGACTCT | 58513 |
rs535872000 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379534 | AAGGTCTACCACCAC[A/G]TCCAGCAGACAGTCT | 58513 |
rs535891053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470133 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 58513 |
rs535891098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463952 | ATGAAGGATCGCCTG[C/T]GCAGATGACAGAAAG | 58513 |
rs535907665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376086 | GAGCACCACTTCCCT[C/T]GCTGGAGCTGATGGA | 58513 |
rs535920285 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362657 | GCCTCCTACAGGCAT[A/G]AGCCACCATGCGTGG | 58513 |
rs535939406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429496 | CCAATCACCAGGGCT[G/T]CAGTCCATGCAGGTT | 58513 |
rs535944770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376525 | CTCCTCAGAGCTGTG[C/T]GTTGAGATGCCTGGG | 58513 |
rs536003893 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16355252 | GCTTCTCTTGTTTTG[C/T]ATTAAAATATTTTAT | 58513 |
rs536023554 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431577 | AAAGTGCTGGGATTA[C/T]ATGCGTGAGCCACCG | 58513 |
rs536071551 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469837 | AGGGTGCTTCCCTTT[A/T]GCCCCCAACCAAAAA | 58513 |
rs536071962 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406669 | ACTAGGGGCTCCAAC[A/G]CCTTTGGCCTGCCCA | 58513 |
rs536073295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444562 | CCAAGGCAGGCAGGC[G/T]GTTTGTCATCTGTCA | 58513 |
rs536074341 | snp | A/G | 3.2963e-05 | 0.00405961 | stop-gained, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403861 | GCTCCGACTTGGCTC[A/G]GTTCAGATCGTCTTC | 58513 |
rs536140146 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16355807 | CTGTTCCGCCTTCTC[A/G]CTCTCCCGCTTGGCC | 58513 |
rs536158843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434737 | GGGAGGCCCTGGCCC[C/T]GGGTCTTGTCCTTCG | 58513 |
rs536196232 | snp | A/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356891 | TCGGCCCCCTCAGGA[A/C]AGCTGCTGCTGCTTA | 58513 |
rs536231747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462654 | GCCTGGGTGACAAAG[C/T]GGGACTCCACCTCAA | 58513 |
rs536271781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413060 | CGCCGGCCAGTGCAC[C/T]AGGTTCAAGGCGTTT | 58513 |
rs536277315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450064 | GTTCTGTACCTGGCT[A/G]TCAACAAGACCCTAT | 58513 |
rs536303543 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450627 | CTGGGATTACAGATG[C/G]ATGCCAACACACCTG | 58513 |
rs536304049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457681 | CCTCCCTCCTGAAAA[C/T]GCTGCTTAAGAGCAA | 58513 |
rs536333521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368597 | TTCCACACAACAGGT[A/G]GTGCCCACACAACCA | 58513 |
rs536339780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426571 | TTGAATCCAGGAGGT[A/G]GAGGATGCAGTGAGC | 58513 |
rs536366948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443996 | ATTAATCCGGGAGGC[A/T]GAGATTGCAGTGAGC | 58513 |
rs536371553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361680 | GGTACCAAGAGGCTA[A/C]AGAAGCTGGGAGGTT | 58513 |
rs536400462 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420744 | TTCAGCCCTGGCCAG[A/T]GGCAAGAGGAGTGCC | 58513 |
rs536411311 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411875 | CGGCTTTTGCAAATA[G/T]TTTTGTAGAAACAGG | 58513 |
rs536417595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430906 | TGGATCATAGGGATG[C/T]GGAGGGACATGGGTG | 58513 |
rs536421825 | snp | G/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424192 | CCCTTGGGAGGCCCA[G/T]ACAAGAGCATTGCTG | 58513 |
rs536430820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400512 | AAAACCCCCAACTTC[A/G]ACCCACAAGGGAGAA | 58513 |
rs536463681 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393691 | AATAAATAAATAAAT[A/T]AAATAAATAAATAAA | 58513 |
rs536468025 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401120 | AAAGCTGATGATGAC[A/G]GGCCCGGGGGCGGCT | 58513 |
rs536475053 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385701 | GCAGGACCAAGCGGG[A/G]CCTGTTCCCAAAAGA | 58513 |
rs536501847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386711 | GATGCAAGCCCTGAA[C/T]TTCATGATCCACTCT | 58513 |
rs536504907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394095 | CTCCCAAGCCTTTCA[C/T]TGCCTTCTACTCCTC | 58513 |
rs536535622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424722 | CTGGAGTGCAGTGGC[A/G]CGCTCTCAGCTCACT | 58513 |
rs536540768 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447637 | TGGTGGCAGGTGCCT[A/G]TAATCCCAGTTACTC | 58513 |
rs536544769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431791 | TGTGTGCATGTATCA[A/C]ACCACCACGTGGACC | 58513 |
rs536573394 | snp | A/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473019 | CTTGTAACTGTTGCT[A/T]ATCAAAGCATACATT | 58513 |
rs536603220 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367109 | TTTCAGAAAAGGGGA[C/T]GGAAATCATGAAAAC | 58513 |
rs536605244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409100 | CTAGGTGTGGCAGTG[C/T]ACACCCTGTAGTCCT | 58513 |
rs536608791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416950 | CTAAGGCACTAGGCA[A/G]GAAGGGGAGCCACAG | 58513 |
rs536610052 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412616 | AAGAGTCTGAGACCC[C/T]ATCTCTATTTGGAAA | 58513 |
rs536644908 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419330 | CGGGCATGGTGGCGC[A/G]CGCCTGTAATCCCAG | 58513 |
rs536669306 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461289 | AGCCTGGGCGACAGA[A/G]CAAGACTCCGTCTCT | 58513 |
rs536689574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367977 | CATGAGAGTGAGAGA[C/G]AGAGAGAGTGTGTGT | 58513 |
rs536692489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375571 | CAAGGATCCCTGAAG[A/G]GCCACTGCCTCTGTG | 58513 |
rs536712150 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419525 | TGGAGTAAGGACAAG[C/G]CCTTTGGCATCTATG | 58513 |
rs536803249 | snp | A/G | 1.72537e-05 | 0.0029371 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421281 | CACAGGCCCCCTGGA[A/G]CCACCCACAGCCACA | 58513 |
rs536817512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401079 | ACTCATGAAGGATGA[A/G]TGCTCATCGTTTAAA | 58513 |
rs536826665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467306 | GGCGTCCGCCAGGAC[A/G]CCAGGCTAATGTTTT | 58513 |
rs536842550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382671 | TAAGTTGGACTCTTG[C/T]TTTTATTCTCAAATG | 58513 |
rs536852305 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398707 | GCTGGAGGGCAATGG[C/T]TATTCACAGGTGCAA | 58513 |
rs536859251 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425862 | GATGCATCCATGAGG[C/T]AGGCCACAGCCATAG | 58513 |
rs536889959 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457865 | CAGTCACCCAAGACT[A/G/T]GGGGGGAGGGGGGAA | 58513 |
rs536892438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468014 | AGGGGGAAAGGAGGA[A/G]GGTGTAGCTCTTTGG | 58513 |
rs536908525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461862 | CCCAAGAGACAAAAC[A/G]TTCCCTTCTGTCAAC | 58513 |
rs536912429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380323 | GCTCTGGCGTCTAAT[C/G]ACACAGACGTGGTCA | 58513 |
rs536932871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422160 | AGTTCACAGCCCTGG[A/G]GCTGGGTCACCCGCT | 58513 |
rs536948587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375085 | ATGCTGCTCATCTCT[A/G]TGCATGCATGTGTGT | 58513 |
rs536950417 | in-del | -/GGA | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441555 | AATCACTTGAACCCG[-/GGA]GGAGGAGGTTGCAGT | 58513 |
rs536967465 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453149 | CTGTCACCCAGGCTA[C/G]AGTACAGTGGTGCCA | 58513 |
rs536996735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422636 | ATGCCTGAAACTGCC[A/G]CTCAAAGTCATTCCT | 58513 |
rs536998401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416322 | CATCACAAGAGTCCA[A/C]CCTGTCCTAGAATCG | 58513 |
rs537002477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418898 | CAGACTTCCACCCCC[C/T]AGAGCCGTGAGAAAT | 58513 |
rs537025989 | snp | C/T | 1.65233e-05 | 0.00287426 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402358 | TCTGCCAGGGAGACG[C/T]CTTCGCTCAGGTTGG | 58513 |
rs537079993 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408999 | GCCAGAGTGGGAAGA[-/T]TCCCTAGAGGCCAGG | 58513 |
rs537082587 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453644 | CGTGAACCCGGGAGG[C/G]GGATCTTGCAGTGAG | 58513 |
rs537101272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389180 | GAATAATAGCTGGGT[A/G]AAGTGACTCAAGCCT | 58513 |
rs537102163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396510 | CTCAACTGATCCTCC[C/T]ACCTCAGCCTCCCAA | 58513 |
rs537127536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433605 | GAGGTGGGAGGATGG[C/T]TTCAGCCTGGCAGTT | 58513 |
rs537158240 | in-del | -/TTTCTTT | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454809 | TCAAGGTTTGAAAGC[-/TTTCTTT]TTTCTTTTTTTTTTT | 58513 |
rs537179054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453002 | AGACGGGGTTTCACC[A/G]TGTTAGTCAGGATGG | 58513 |
rs537189061 | snp | C/T | 6.67468e-05 | 0.00577658 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403911 | TCCTGAGATTGGATT[C/T]GCGTTTTCAGTGATG | 58513 |
rs537219852 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461830 | AGGCGGCTCTGGGCC[A/C]TGTGCCTGTTTCTTC | 58513 |
rs537222412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428060 | ACAAAAATGAGGTGG[C/G]CATAGTGGCAGGTGC | 58513 |
rs537224190 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472070 | AGGGCGGGGCCGTAG[A/G]CAGGGCCACGCATGT | 58513 |
rs537274864 | snp | C/T | 3.41151e-05 | 0.00412994 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377100 | GGTAGGCGGTGGCTG[C/T]GAGAGAAGAAAGCTT | 58513 |
rs537283037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383277 | CCCTGGTTTCAGGGC[C/T]CAAGGACAGGCAGAG | 58513 |
rs537287005 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465080 | CGAGACTTAGTCTCA[A/G]AAAAAAAAAAAAAAT | 58513 |
rs537288115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370060 | AAGATCCCTGAGAAC[A/G]CCGTGCAGCGAGTCT | 58513 |
rs537319186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363188 | CCTCTATCTGCCCAA[C/T]GGAGTCCCTGGGCAT | 58513 |
rs537344511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371993 | AGTTTCTTCTGCCCA[A/G]AACAGACACCTGCTG | 58513 |
rs537373599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459367 | GCTGCTGTAATGACC[A/G]GCCCCTCTCACTACA | 58513 |
rs537408965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439679 | CTGGGCAACAGAGCG[A/C]GGCTCAAAAAATAAA | 58513 |
rs537460763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393366 | GAAAAAAAATAAATC[G/T]GTCGGGCATGGTGGC | 58513 |
rs537480217 | in-del | -/AAAAAAT | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439685 | AACAGAGCGAGGCTC[-/AAAAAAT]AAAAAATAAAAAAAC | 58513 |
rs537517684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471182 | AGTGTCACCTCCAGG[A/T]AAGCAGCGACCTTGT | 58513 |
rs537519730 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394362 | CCCTGGGTAAGAGGA[C/T]ACAGGACCCTGGGCT | 58513 |
rs537669712 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358239 | GGTGCCTTCAGAGTC[A/G]ACCGGTTCAAGGCCA | 58513 |
rs537679228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455823 | CCTTCCACTGGCTCC[A/G]GGTAAAAATGTACCC | 58513 |
rs537692309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366928 | GCTAACTCCTTAATC[A/G]TTTTTTCCGATTTTG | 58513 |
rs537709877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399217 | ATTCAGGAGGTCAGG[A/G]TAACTAATAGTGGTT | 58513 |
rs537724198 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367670 | CGTTCTTGGTCAGCA[A/G]AGTTTTTCAAGGTTC | 58513 |
rs537741861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452512 | GTAGTCCCAGCTACT[C/G]GAGAAGCTAAGGCAG | 58513 |
rs537744236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438915 | CTCGGCCTCGTTGAA[C/T]GGAACATCCCCTGCC | 58513 |
rs537754363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356730 | ATAAAAACTTAAAAA[A/G]GGGAGAAAACCATCT | 58513 |
rs537762175 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363557 | CCCAGGTGTCCTTGT[A/G]GGCTCCGGGGCTACA | 58513 |
rs537765148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360373 | TATAGACCCCCAGTG[C/T]GCATCTAGGGTCAAC | 58513 |
rs537782645 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408223 | GGTTAGGAAGGGGAG[C/G]TCAGAGCAAAAAGAA | 58513 |
rs537787795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405654 | GAACGGGATGGCGCC[A/G]TGTGCTTTGCCTTAC | 58513 |
rs537809346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436821 | CTGACACAATCATCC[C/T]ATAAAATGTTCTGAA | 58513 |
rs537836113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466467 | GGGCTCATTTCTTTA[C/T]ATCTGGGCCCCTCCC | 58513 |
rs537845484 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406235 | TCATGCCTCAGGAAG[C/G]TGGGGTCTCCGTTCC | 58513 |
rs537879404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384954 | TCAGGGCTCACCCCA[C/T]GGGACTGCAGTGCAT | 58513 |
rs537897594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467094 | AAACAAACATCTAAG[A/G]ACCTAAACATTGAAA | 58513 |
rs537898843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385827 | CACAACATAGGCCAG[C/T]ACCTGGGGTCAAATT | 58513 |
rs537912996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468072 | AGCCCAGTTACCACG[C/T]GCTTCCTAGGTACAG | 58513 |
rs537914093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454668 | TGGGGCATGGCACAG[G/T]GGTAAGGCCTACAGT | 58513 |
rs537916212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379725 | CATCTAAGGCTCCAG[C/T]GTCTAGTCACACAGA | 58513 |
rs537917775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373703 | GAATTGTACAGAGCC[C/T]GGCTCTGATTCCCTT | 58513 |
rs537920877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437203 | GATGTCCAAACAAAT[C/T]CTTGTACATGAATGC | 58513 |
rs537927480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430957 | GATGTATGCATGGCC[A/G]GGCACAGTGGCTCAC | 58513 |
rs537934919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424892 | GGTCTTGATCTCCTA[A/C]CCTTGAGATCTGCCC | 58513 |
rs537955207 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374631 | CAAAAGCAGACCCAG[C/G]GCCGGGTTTAGGTAC | 58513 |
rs538005797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358983 | AGGGAAGAGGTTTCC[C/T]GGGAACAGCCACACA | 58513 |
rs538033737 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411697 | CTAGCACCACCCCAT[A/G]TTACTTATTCATTTA | 58513 |
rs538044354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405374 | TGTGGTGGGGAGCCC[A/G]GTGGGATGTGTGAGT | 58513 |
rs538054747 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461319 | TTAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 58513 |
rs538063343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412301 | GGTCAGGAGATTAAG[A/T]CCATCCTAGCCAACA | 58513 |
rs538108804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384174 | GCCCCTGCAGCCCCC[C/T]GAAGACAGAGCCCAT | 58513 |
rs538137431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429057 | TCTTTATTGTCTTAC[A/G]GAGACATCTTAGAAA | 58513 |
rs538143037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443447 | GGCGCAGTGGCTCAC[A/G]CCTATAATCCCAGTA | 58513 |
rs538195156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423536 | GATTGCACCACTGCA[C/G]TCCAGCCAGGGCAGC | 58513 |
rs538211358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420822 | TGAGGCCGACTCCTC[A/G]ACTGGGCTCTGAGGC | 58513 |
rs538226891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384600 | AGGGCCGGACACCAA[C/T]GGGTCCAGTCTGGTA | 58513 |
rs538258690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424087 | GCTTTAAGGCCGGCT[C/T]AGCAGCCACAGGTCC | 58513 |
rs538281012 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376884 | TTTGTGCACTCCAAT[-/AC]AGAGCCAGAAGCCCA | 58513 |
rs538291913 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451568 | GAGTTTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 58513 |
rs538345271 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473413 | CTCAGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA | 58513 |
rs538351315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370901 | CTCCACCTGGTTGGC[C/T]GTTTTAGGCTCCTTG | 58513 |
rs538369139 | snp | C/T | 6.5975e-05 | 0.0057431 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417998 | TGTCCGGCGAGAGGA[C/T]TTGAGGAGGGTCGAT | 58513 |
rs538381040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407595 | TCTCCCAAAGTGCTG[A/G]GATTATAGGTGTGAG | 58513 |
rs538410429 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432484 | GAGGCAGGAGAACGG[C/T]GTGAACCCAGGAGGC | 58513 |
rs538425599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417732 | CAGGGATAAAATTGT[C/T]CCTTTAGTACACAGG | 58513 |
rs538455164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398160 | GGTACAGAGTTAAGA[C/T]AAGCCACCGGTCTGG | 58513 |
rs538456892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391343 | CAATACCAGGAATGC[C/T]AGGGAAATTCTCACT | 58513 |
rs538462761 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447992 | AAGGTGCAAAAGTAT[A/T]TCAGGAGGAAGGAAA | 58513 |
rs538521060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432942 | CTAGAGTAGCTGGGA[C/T]TACAGTCACGCACCA | 58513 |
rs538521876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470178 | CTCGAGTTCAGGAGT[C/T]TGACACGAGCCTCGC | 58513 |
rs538566853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382097 | GCCGCCTAACCCTCC[A/G]GGCTGACCGGGGACA | 58513 |
rs538579991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427259 | CACTGCACTGGAGCT[A/G]GGGTGACAGAACAAG | 58513 |
rs538599247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426665 | AACGACAACAAAAAA[A/G]CAAAAAGTCCACGTC | 58513 |
rs538614729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470853 | ACTGAGTGCCTCTCA[C/T]ATGCTAGGCACTGTT | 58513 |
rs538641624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421152 | TTCGAGCCTTGGCAC[A/G]TGCACCTTGCTCAGC | 58513 |
rs538655273 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414546 | GCTGGGACTACAGGC[A/G]CGTGCCACCACGCCC | 58513 |
rs538655785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382421 | GCAAGAGTGAAGTGT[A/G]CTTAAAATAAAAGGA | 58513 |
rs538693956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376967 | ACATACGGCACTTGC[A/G]TGGACCTGGGCAGCT | 58513 |
rs538720043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401162 | CTCATTACGAGTCCA[C/T]GAGAAAAGAGAGTAT | 58513 |
rs538747772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438118 | AGCACTTTGGGAGAC[C/T]GAGGCAGGTGGATCA | 58513 |
rs538765652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415253 | GCAGACCCGATCTGC[C/T]GGTATCTGGAGGTTG | 58513 |
rs538774106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356004 | ATGTCTTGGCTGGGC[C/T]CAGTGGGCGTGCGAG | 58513 |
rs538779667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356620 | CGGCTCTGAGGGTCA[A/G]TTTCTCCCAGAACAC | 58513 |
rs538826795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401493 | CGGAGAGAGCTGCTG[A/G]AGGCAGCAGAGCACC | 58513 |
rs538835832 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394267 | CCACACAGACTGGAG[C/T]TGGGGAAGACACAGA | 58513 |
rs538838165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386560 | GGTTGAGTTTCCATT[C/T]CGCCAGCTACAGCAG | 58513 |
rs538842762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468753 | TGCAGTGGCTGACAC[C/T]GTAATTCCAATACTT | 58513 |
rs538871728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387791 | AAAAAAACCCCACTT[C/T]ATTAGGTTAGCTAAA | 58513 |
rs538873761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394867 | TGGTGAGCTTGGAAC[A/G]CTTCCCACTGTATCT | 58513 |
rs538887920 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380994 | CAGAACAGGGAGGTG[A/G]CCCCTCTAAGAGGCA | 58513 |
rs538908462 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419998 | CGGCTCTGACACCAC[A/C]TCCTGCTCTGCTGAC | 58513 |
rs538909545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388409 | CAAAGCCTAAACAGT[A/G]TAAACACCAAGAAAA | 58513 |
rs538927299 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357083 | ACCCAAGGACCCAGG[C/T]TCTCGAGGAGGGCCC | 58513 |
rs538974534 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419887 | TTCTCTGCTCCTGCC[A/G]TCTCTCAAGGAGTGT | 58513 |
rs538990101 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454819 | AAGCTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTA | 58513 |
rs539012168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406490 | GGTAGCCCAATGCTC[C/G]GAGCGATGCTCCCAC | 58513 |
rs539038139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410375 | TGGGTAAGTGTTGGT[A/G]AGGCTGTGCAGAGCT | 58513 |
rs539078863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369213 | TGCAGGCACCAGCCC[C/T]GCGCGCACTCTGCCT | 58513 |
rs539106192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443791 | CTGTGAATGTATAAA[G/T]AAGTGAAAGTTGTAA | 58513 |
rs539113650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362227 | CCCATACACAACGCA[C/G]ACAGAGCAGCTAAAA | 58513 |
rs539140954 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428214 | TCAAAAAAAAAAAGA[A/C]AGAAAGAAAGAAAGA | 58513 |
rs539205894 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374356 | TCAACCACAGCAGAA[A/C]AAAGATGCAGTGGCC | 58513 |
rs539288589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462891 | AAAGGAGGCACAGGC[A/G]CCCTCTTCCTCCTGT | 58513 |
rs539300708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457043 | CTGCAAGGAGCAGGG[A/C]TGGAAGGAAGTGATC | 58513 |
rs539301630 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403262 | GAAGAGGGTGGGGGC[A/G]TCCCAGGCAGCTTAG | 58513 |
rs539304992 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375625 | GATGGAAGGGAGTCC[C/G]TTTGTTGTTTTGTTT | 58513 |
rs539313080 | in-del | -/ACAT | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458748 | CACTCAGGCTCACCC[-/ACAT]ACACTCACACTCACA | 58513 |
rs539324605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375982 | ATGCGGAGCCTGCTA[G/T]GTCCATTCCAGGACC | 58513 |
rs539332826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450758 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 58513 |
rs539344416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368668 | CCCTACACAACAGGC[A/G]ATCTCACAAAACCAT | 58513 |
rs539378727 | snp | A/T | 0.077417 | 0.180873 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417464 | TGTGATGAGCAAACT[A/T]CCAGGTGAGCCTCTG | 58513 |
rs539447317 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456227 | CAAAAAACCCTCCTG[A/C]AAAAGGGTCCACCCT | 58513 |
rs539455739 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448549 | GTATTAAAAAAAAAG[C/G]GGGGGGGAGAAAGGC | 58513 |
rs539478083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398197 | AATGAGTGTGAATCA[G/T]CATGAGTGCCGCTTC | 58513 |
rs539485242 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390091 | CTTCTGACTGGATTT[A/T]AAAAAAAAAAGCAAG | 58513 |
rs539502188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401452 | AAGGGCTCCAGGGAG[C/G]AGCCCTGGGAGAGAG | 58513 |
rs539511257 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465138 | GAAAGTTTACAAATT[A/T]GTGTTGGGCTGCATT | 58513 |
rs539519841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390728 | TATCTGGAAATGAAA[C/T]AACATACTTTTAAGT | 58513 |
rs539521822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383310 | CGGTCATTAGATCCC[C/G]GCCCTAGCTCAGGCT | 58513 |
rs539528701 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428235 | GAAAGAAAGAAGGCC[A/G]GGCACAGTGGCTCAC | 58513 |
rs539558476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377884 | GGGCTCTGACCACCT[A/C]TGGCCCGGACCCTCG | 58513 |
rs539598357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465709 | GAAGACAATAAGCAG[C/G]CCTTTCCATGTCCCT | 58513 |
rs539645063 | in-del | -/ACATGCACATACAC | 0.0185938 | 0.0946107 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437687 | AAAACATGGAAATAT[-/ACATGCACATACAC]ACATGCACATACACA | 58513 |
rs539682768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459480 | TGAGATTAAAGTGTT[A/G]AGGGAGGCAGGTGGT | 58513 |
rs539687499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363639 | TCCCAGCTGGCCTCC[A/G]TTTCCTTATCTGTGA | 58513 |
rs539695260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460278 | GACAGAGCCTGTCTC[C/T]AAAAATAAAAAAAGA | 58513 |
rs539695268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453763 | ATGTTCACTACCAGG[A/G]TGACAGGATCCGTAT | 58513 |
rs539705061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395926 | CTCCAGCCTGGGCGA[C/T]AGAGTGAGTCTATCT | 58513 |
rs539725467 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357371 | CTCAGTGCCCGACCT[A/T]GGGGTAGCCAGGATG | 58513 |
rs539726135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364323 | GCAGTGCCCAGCCCA[C/T]GCGGGCAGGACAGGA | 58513 |
rs539733403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359733 | CAGATGTGGTGGTGC[A/G]CGCCTGAGGTCCCAG | 58513 |
rs539801162 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363612 | TGGGCCTCGGCAAGG[C/G]AAAGTGCCTCCTCCC | 58513 |
rs539808509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434230 | TGGACCCACAGGAGC[A/G]CTGATGAAAGCCCCT | 58513 |
rs539817537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396536 | CCCAACGTACTGGGA[A/T]TATAGGCATGAGCTA | 58513 |
rs539817964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424852 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 58513 |
rs539824920 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395063 | CAACTCTACTAAATA[C/T]ACAAAAATTAGCCGG | 58513 |
rs539850967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462072 | GGCAATCATAGGACA[A/G]AATGGTGGCTTTGGA | 58513 |
rs539874658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380460 | AGCCGTCTAAGGCTC[C/T]AGTGTCTAGTCACAC | 58513 |
rs539886346 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472893 | GGCCAGAGAATCACT[G/T]GAACCCGGGAGGTGG | 58513 |
rs539923795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375317 | GCATGTGTCTGCAGG[C/T]GTGGAGGATGTGTGT | 58513 |
rs539959189 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366737 | GTCAGCCGAGTGCCC[A/G]GTCCAGCTCTCGACC | 58513 |
rs539974594 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377069 | GGGAGGCCCTGGTCC[C/T]CCGCCATCCGGCACC | 58513 |
rs540040580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408833 | TAGGTCAATGGGATA[A/G]AGCTGAGGGTCCAAA | 58513 |
rs540061838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453047 | CCTCATGATCTGCCC[A/G]CCTCGGTCTCCCAAA | 58513 |
rs540073479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392809 | CTGTAATCCCATCAC[C/T]TTAGGAGGCTGAGAT | 58513 |
rs540095451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385338 | ATTTATTCATTAGAC[A/T]CGTGTGTCTGCATGA | 58513 |
rs540114705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446873 | TGACCTGCCATTTCC[C/T]CAGGAAAGCTGAGAC | 58513 |
rs540136262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453480 | ACACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAT | 58513 |
rs540140241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440722 | TATTTCAAAATGAAA[A/C]CTTCCCGTGTTAAGT | 58513 |
rs540195289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418479 | AGCCCTTCCGTGGAA[A/G]TGGGTGCTGAGACCA | 58513 |
rs540211436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454848 | TAAGAGACAGCTCTG[A/G]GCCAGGCATGGTGGC | 58513 |
rs540235765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441777 | TCTGCAGCGACCAGG[A/C]CACTACCCAGGAGGC | 58513 |
rs540259250 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374829 | ACGTATGTAAGCACA[C/G]AGTGTGCATGCCCGG | 58513 |
rs540282916 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461777 | GGCCCCAGCCCTGGT[-/G]GTGCCCTGACTGCTG | 58513 |
rs540297215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456426 | CTTTGGGAAGCCAAG[A/G]TGGGTGGATCACATG | 58513 |
rs540329268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449565 | TGACTCTGGAAACAG[A/T]CTGGCAGTTTCTTAA | 58513 |
rs540393281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442791 | CAGGGAAGGAAGGAA[A/G]TGCAGTGTCCTCAGC | 58513 |
rs540405223 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392269 | CACACAGAGCAGGCA[C/T]GCAGCTCTCCCGGGC | 58513 |
rs540470402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436262 | GCCACATAAACGTGA[A/G]GAAATGTGACAGTCT | 58513 |
rs540471828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466486 | TGGGCCCCTCCCAAC[A/G]ATGTCAGCCCCGTGA | 58513 |
rs540482298 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404184 | GAGGGGCATGACCAA[A/G]CACGAACAATCTGTC | 58513 |
rs540489339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460598 | TTGCACCCTGGTGAT[A/G]GACAACCTTGCCCAG | 58513 |
rs540528487 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424336 | CCTCCCACCCCACCC[C/G]ACCAGGGGCCACTGG | 58513 |
rs540544013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431014 | GAGTCCAAGGCAGGC[A/G]GATCACCTGAGGCCA | 58513 |
rs540545510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379236 | CGTGAACCTGGGAGG[A/C]GGAGCTTGCAGTGAG | 58513 |
rs540549046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467580 | GTCAATAAGTGACAG[C/T]CAGGGAATTCTGGAT | 58513 |
rs540549564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423647 | GAGCAACCTGATTTT[C/T]ACTTGTGGCATTGTA | 58513 |
rs540560411 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438533 | TGGACCAAATATGTG[C/T]CGAATTTTTGTTTGT | 58513 |
rs540577532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, splice-donor-variant | EPS15L1 | GRCh38.p7 | 19:16373914 | CACGGTCTGTACCTA[C/T]CACCCAGCAGCGAGT | 58513 |
rs540607609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452267 | CCTGGCCAACATGGT[G/T]AAACCCCATCTCTAC | 58513 |
rs540612368 | snp | A/G | 6.61529e-05 | 0.00575083 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417617 | AGTAAACTCCCCGGA[A/G]CCGAGAGAGCCTGAA | 58513 |
rs540639175 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445543 | GGAACAATGGACTCA[C/T]ACCTGCACGCTGCCC | 58513 |
rs540676116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363256 | AATAATATGCAACAC[G/T]ATTCCGGCGTGTTAA | 58513 |
rs540684462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446471 | TCACTGTAAAATGTT[A/C]AGAGAAGTACCTATA | 58513 |
rs540711242 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, missense | EPS15L1 | GRCh38.p7 | 19:16356977 | GCTCTCTGCTCAACA[A/C]TGGAGTAACACCAAA | 58513 |
rs540714236 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445881 | CAGCAGAGCTGACCC[C/G]ATGTGTTCTCCTGAC | 58513 |
rs540715202 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418598 | TGATGAAGAAAGAAT[C/T]AGCAACGACTCTCTT | 58513 |
rs540750203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357425 | ACTGAGGAGGGGCTC[A/G]TGGGCCCCAGGAAGG | 58513 |
rs540754544 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416117 | CAGGGCTCTGCTAAC[A/G]GCACAAAACCAAGGC | 58513 |
rs540757363 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427385 | TTCTGAATTTCTGAA[C/T]GTGTGTATTACACTT | 58513 |
rs540765615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398439 | ACCACAAGACACACA[C/T]GCCCAGCAAGCGTCT | 58513 |
rs540803982 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375103 | CATGCATGTGTGTAC[C/T]GACAAGAGAATATGC | 58513 |
rs540809329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395269 | ATGTCCTTACTTTTC[C/T]AGTTGAAGAACCACT | 58513 |
rs540814637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465970 | GGACGTAACAATCTC[C/T]GGCCTCACTTTATCT | 58513 |
rs540824330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384246 | GCAGGTGTCAGGGAC[A/G]GGACACACCTCATCT | 58513 |
rs540838001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420465 | AGACCCACTGTCCCT[A/C]GCCAGTTGGAGGCGG | 58513 |
rs540859565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378659 | GAGCAGATACTAAGC[A/G]CCGCCACCTGGGGGG | 58513 |
rs540897337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451677 | GAGACTACAGGTGCC[C/T]GCCACCTCACTCGTC | 58513 |
rs540903091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376188 | TCCTGTGGCTGCCCA[A/C]AATTCAGGGACAGTG | 58513 |
rs540914283 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378131 | GTGGATGGATGGATG[A/G]ATGGGCAGGTAGAGA | 58513 |
rs540938393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362834 | TTTTTAGCCCCCACT[G/T]CTGTCCCTCTGGTGT | 58513 |
rs540941747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369794 | ACTGGCAGGTGTCAC[A/T]ATTCTGGCTTCTTTG | 58513 |
rs540971826 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410150 | AAAAAAAAAAAAAAT[G/T]CAATTTAAAAATCGG | 58513 |
rs540985928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407928 | TGGGACAGAGACTGT[C/G]TCTCCAAACCCCTGA | 58513 |
rs541030431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375750 | TAAATCCACACAGCC[C/G]ATACTTGGTCATACT | 58513 |
rs541046376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393774 | TGGACCTGGGGAGGG[A/G]AGCCACCTCCAGAAG | 58513 |
rs541053788 | in-del | -/AAGAGGACACAGGACCCTGGGC | 0.134119 | 0.221521 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394354 | GCCAGCTCCCTGGGT[-/AAGAGGACACAGGACCCTGGGC]AAGAGGACACAGGAC | 58513 |
rs541078845 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381934 | GCTGGCTTCTGGGCC[A/G]CATCTCCAGACTCGG | 58513 |
rs541126517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432512 | GGCGGAGCTTGCAGT[A/G]AGCAGAGATTGCGCC | 58513 |
rs541139791 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440231 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 58513 |
rs541149245 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433257 | CTCAGCCTCCCAAGT[A/G]TCTGGGATTACAGGC | 58513 |
rs541169925 | snp | A/T | 0.0637235 | 0.166737 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402557 | GACGCTTTTTTTTTT[A/T]AAAACACAGGGTCTC | 58513 |
rs541185513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405950 | GGTGCAAGGGGCCAT[C/T]AGGACGCAGGAACTG | 58513 |
rs541185615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413335 | TGTCCAAGAAGCTGC[G/T]CATGATGGCTAGTAT | 58513 |
rs541223184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381819 | AACATGTCCCTGGGC[C/G]TAGGGCCCGTGCGAG | 58513 |
rs541226375 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359684 | TGGGTAGTAAAGTGA[G/T]ACCTTGTCTCTATCA | 58513 |
rs541226646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464591 | TTTGGCCCTTTGACC[C/T]AGACCTGCAGCCTCT | 58513 |
rs541245974 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406527 | CGGAAGCCTCTAGAG[A/C]CTCCTAAGTCTAACC | 58513 |
rs541287446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458188 | GCCAGGTCAGTGCCA[C/T]GCCACCTTCCTCCTC | 58513 |
rs541300125 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420924 | CTGCCCCCGCCCTCA[A/C]CCTGCCAGGCCACTC | 58513 |
rs541327001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370259 | GCAGGCAAGGGGCGC[A/G]CTGACTCAGGGCTTT | 58513 |
rs541367812 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468320 | AGCAAGGTTAGGTGG[A/G]GTCGATTCAGGGCTT | 58513 |
rs541397658 | in-del | -/AT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412647 | AATATATATATATAT[-/AT]TTTTAAAAACTTCTT | 58513 |
rs541405280 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400771 | TGCCCTGCCCAAAAG[A/T]TGAACAAAAATAACC | 58513 |
rs541423585 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469340 | GGGCTCCAGTGTTGC[A/C/G]GAGTTCGAGGAGGAT | 58513 |
rs541424099 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370862 | CAGTGCTGGGGGATG[G/T]GGGGCGTGGGCAGGA | 58513 |
rs541425534 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412745 | TCAGAGGCCCTGGGA[G/T]GGGCAACCACAGTAA | 58513 |
rs541435543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394320 | CTTCCCATGCTGGGT[C/T]TCCTTTATCCCATCT | 58513 |
rs541451861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438125 | TGGGAGACCGAGGCA[A/G]GTGGATCACCTGAGG | 58513 |
rs541455656 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393581 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 58513 |
rs541457787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429177 | AGCTGGGCAGGGCTG[C/T]GAGCTCATGTCTGAG | 58513 |
rs541462960 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401672 | ACACCTGTCTTGGTA[C/T]CAGGGGCTCAAGAGC | 58513 |
rs541476937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392145 | ACTCAGCAGGAATGA[A/C]ATCAGCCTGGGATAC | 58513 |
rs541491608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381517 | GAGCTCGGAAGGCTC[C/T]GGCAAGAAGGAAATG | 58513 |
rs541495256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435701 | GACTTGCTGACTCAG[G/T]GCCTTCAGAAGCCCA | 58513 |
rs541516023 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384771 | CACTTTCCCTGGACG[C/T]CTCGCACCTGCAGGC | 58513 |
rs541519168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429693 | CCTCAGCCTGGCAGA[A/T]GGGGCCCTGTCACCT | 58513 |
rs541590378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403597 | CCCTGCGCCTCCAGG[A/C]CAGCACCACAGCCTC | 58513 |
rs541616604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457136 | CACAATGCAGACACC[C/T]GGAGAAGGAGGACAT | 58513 |
rs541622480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450202 | CAGTGAGCTATGATC[A/G]TGCTACTGCACTCCA | 58513 |
rs541628923 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413366 | CAATGACTGCTACAC[C/T]TCAGCCAGGGGCTGC | 58513 |
rs541643700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404059 | CACCTAACCCAGGCC[C/T]GACACCTGGCTTCCT | 58513 |
rs541661577 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397097 | TTTCTTTCTTTCTTT[C/T]TTTTTTTCTGAGACA | 58513 |
rs541664763 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471217 | CTGGAAGAATGCAGC[A/G]CTCCCAGCACCTGAC | 58513 |
rs541688861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441006 | CATCACTGGCCTTGC[A/G]GGGCAGGAGTGACTG | 58513 |
rs541707476 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365237 | AGCCTGTTTCTTAAT[A/C]CAAACAAAGGGCTGT | 58513 |
rs541713787 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460033 | GTAATCCCAACACTT[C/T]GGAGATTAAGGCAGG | 58513 |
rs541731564 | snp | C/T | 1.8283e-05 | 0.00302344 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361805 | CTGCAAAGCCCGAGG[C/T]AGAGGCCTTAGAAGG | 58513 |
rs541768361 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355538 | GGCTTCCCCAGGAGA[C/T]GTGACCTTTCCAGGT | 58513 |
rs541790130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391517 | GGAGGGTGAGTGCCC[A/G]TCTCTGAGCAGGCCC | 58513 |
rs541812301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383383 | ACAGATCCAGCCTCC[C/G]AAAGGAAGAGGAGTC | 58513 |
rs541828892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384315 | TCAAACAGGGAAACA[C/T]ACAACTCACAAGGAA | 58513 |
rs541840209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458906 | TCCTGAGAGTTGCAT[C/T]GTCAGGTTAATTTCA | 58513 |
rs541849076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377891 | GACCACCTCTGGCCC[A/G]GACCCTCGGTCAGCC | 58513 |
rs541861965 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421922 | CTGCCCTACAGGCAG[C/T]CAAAGTGTCCTGTCC | 58513 |
rs541885483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371442 | CCGCTGGTTAAACTT[A/C]GGTAAAAGCTGTTCG | 58513 |
rs542026023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453810 | ATGCAATACTCTCAT[A/G]TAACAAATATGCACA | 58513 |
rs542026809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471470 | GATCAGTCTGAGATC[A/G]CACTGCTGCTGACGG | 58513 |
rs542038632 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388986 | TGGCACAGTGGCTCA[A/T]GCCTGTAATTCTATC | 58513 |
rs542072057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382823 | AAGAGCCTCCCAAAG[A/G]AAACTTCTAGAATCA | 58513 |
rs542083227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358194 | ACGGGTCTGTGTTTC[C/T]AAATGAAAGGTGTCA | 58513 |
rs542089287 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448009 | CAGGAGGAAGGAAAG[A/C]CTTTCCACAAAGGGC | 58513 |
rs542090050 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472181 | TCTTCCGTGCTCTCT[A/T]GCCCGTTCCCCTACT | 58513 |
rs542128723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464948 | GCCAGGTGTGGTGGC[A/G]GGTGCCTGTAGTCCC | 58513 |
rs542132261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358734 | AGGTGTCTGATGGCA[C/T]TTCCACCCCACCATG | 58513 |
rs542171842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421727 | TCCACCCCATCACCC[A/G]CTCTCCTTGTCCATC | 58513 |
rs542190651 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465281 | GCCCCTCCTGCAGCT[G/T]GGACCACCCGTGACC | 58513 |
rs542203641 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360776 | TTGACAAATAAGCCA[C/T]AGGATAGCTGTGCAC | 58513 |
rs542208489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375376 | CATACACGTGTACGT[C/G]CACATACATGCATAA | 58513 |
rs542294291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416533 | CTCTCAGCTTCCTGG[A/G]AGGGTGAGTGGGAAG | 58513 |
rs542299421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453294 | ATTTTTTGTAGAGAC[A/G]GGGTCTTGCTTTGTT | 58513 |
rs542310426 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364703 | GCAGCTCTGGCGGGC[A/G]GGGGTCAAGTGAGGC | 58513 |
rs542321341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368807 | TGTCATTCACCCTAC[A/G]CAACAGGTGATCCCA | 58513 |
rs542343827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413575 | CTGTGGCTACAACAT[A/G]GGGTTTTTATACAAG | 58513 |
rs542357296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409482 | CAGCAGCAAAAAAAG[G/T]ATAAACCAGACTTCA | 58513 |
rs542359984 | snp | C/T | 0.000216679 | 0.0104064 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361913 | CGCCGCTGTCAGCCC[C/T]GAGTGGCTGGAATGG | 58513 |
rs542390158 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396107 | AGACCCTGTATCTTT[A/T]AAAAAAAAAATTAAT | 58513 |
rs542419111 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442231 | GAATCTGTAAATGAA[A/T]CCACAGATATTGGTC | 58513 |
rs542423551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431257 | AAAAAAACTTTTTTT[A/T]AATAAATAAATAAAT | 58513 |
rs542425003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389439 | AGCCTGGGCAACAGA[C/G]TGAGACTCTGTTTCA | 58513 |
rs542433832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393504 | AATACAAAAAATTAG[C/T]CGGGCGTGGTAGCGG | 58513 |
rs542441441 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433747 | CGAGGCGGGTGAATC[C/T]GAGATAGGAGTTTGG | 58513 |
rs542456396 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454126 | AGGGTAAGAGGGTTC[A/G]CTGTTTTCCCCCCTT | 58513 |
rs542552159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428312 | GGCAGGAGATGGAGA[C/T]CATCCTGGCCAAGAT | 58513 |
rs542564635 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424047 | GCAGCCTTGCCGTGG[A/G]GCTGGCTCTCCCAGT | 58513 |
rs542582575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412914 | CCTGGTCAAGGACAT[A/G]AAGATCAAGTCCCTG | 58513 |
rs542591226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456526 | GCTGGGCGTGGTGGC[A/G]GGTACCTGTAATCTC | 58513 |
rs542633977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368298 | CACAACAGTGGACGC[A/C]CACATACAACCATCA | 58513 |
rs542643481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442865 | AGACATCGCTGTTTG[C/G]AGGTCACTTCCCCAT | 58513 |
rs542658604 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466630 | CATGAGGGCCAGGCG[C/T]GGTGCCTCCTGCCTG | 58513 |
rs542693638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359876 | CCAAATATGTAAAAA[C/T]CAAAAACTTAGGGAA | 58513 |
rs542701044 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406664 | AGGACACTAGGGGCT[C/T]CAACACCTTTGGCCT | 58513 |
rs542704894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443639 | CGCTTGAACCCAGGA[A/G]GCGGAGGTTGCAGTG | 58513 |
rs542729642 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357974 | GACAACAGTGGGAGG[-/GA]GAGACAGTGCAGCTG | 58513 |
rs542739483 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434538 | AGAGCACACCTGTGT[A/G]AATGTCCAGACCGAG | 58513 |
rs542761564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451418 | ACCAATACCAAAGGC[A/G]TTATTATTAGTTGTG | 58513 |
rs542783292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385448 | AGCATCATTCACGGT[A/C]ATCAGAAGAGTGACA | 58513 |
rs542825915 | snp | A/C | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442199 | GTAATAAGATTCATA[A/C]AACGAATTTCCAGTG | 58513 |
rs542855214 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378373 | CCCCCCAGCCGCTGA[A/C]TCAGCCTCCTGTTTC | 58513 |
rs542868261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448958 | TCAAATTCAACAGCA[C/T]AAAAAAGAAAACAAT | 58513 |
rs542881122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462205 | TGGCACCATTGTTGG[A/T]CCCACAACATTCCCT | 58513 |
rs542910119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455495 | CGATGCACTGCCCTG[C/T]GGAGGATGCAGGACT | 58513 |
rs542920747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468346 | GGCTTACTAAGGTCA[C/T]CAAAGCTGACTTTTT | 58513 |
rs542931667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449624 | CAACATGAAACTACC[A/G]CATGAACCAGCAACT | 58513 |
rs542938888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418171 | TGAACCCAAGTCACC[A/G]ATCCCTTGCTTTTCA | 58513 |
rs542953707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425496 | TATGTGTAACTTTCC[A/G]AGACATGTGTTGAAT | 58513 |
rs542955132 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367184 | TCAAACCAGGTGCCA[C/G]GCATCATCCTGGCAC | 58513 |
rs542998217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411960 | GGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 58513 |
rs543004729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405438 | AGCTCTCTCTGACCC[C/T]GTGGGATGGATCCAG | 58513 |
rs543031872 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419019 | AGGGGCATGGCCACA[A/G]TGCACAGGACAGTCC | 58513 |
rs543044213 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440541 | GATACACAGGAACCC[A/T]CCAAGCTATTTGTGC | 58513 |
rs543098056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436358 | GGAATTCTGTACTTA[C/G]AAGACAGCCCTCGTT | 58513 |
rs543105539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440849 | CATTTGCTCTGTGTA[C/T]ATGTGTATATACCTG | 58513 |
rs543107593 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395977 | TCAAGGTGTGGTGGC[A/G]TGTACCTATAATCCC | 58513 |
rs543144594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433917 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 58513 |
rs543147097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392954 | GGCTGAGGCAGAAAG[C/G]CTGCTTGAGCCCAGG | 58513 |
rs543148030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471559 | CTCGCTGGGCCGCCG[C/T]GCCGACAGAAACGCT | 58513 |
rs543152572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427889 | ACAGAGCAAGACTCC[A/G]TGTCAAAAAAAAAGA | 58513 |
rs543178600 | snp | A/C | 7.04349e-05 | 0.00593401 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417685 | TAGCAACCTGACATC[A/C]CCTGACAGGAGGCAC | 58513 |
rs543202887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414703 | CACGCCTGGCCTTTT[C/T]TTGGTTTTGTTTTTT | 58513 |
rs543228028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415528 | CATTTCCACAAGCCC[A/T]GAAACTTACAATACA | 58513 |
rs543236672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379353 | CCTCCAAGAGCATAG[A/G]AGAGAAAGATCAGAG | 58513 |
rs543252035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454861 | TGGGCCAGGCATGGT[A/G]GCTCACACCTGTAAC | 58513 |
rs543256230 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459423 | ATCACGCTGTGCCCT[C/G]CTAGAAGCAGGCCTT | 58513 |
rs543265824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408050 | ATCTAAGGGGAGTGA[C/T]GGATAAGGGAAGGGA | 58513 |
rs543268535 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366397 | CCCTTGGTTTGGGGG[G/T]TTTAAAAAAAAGAAA | 58513 |
rs543292563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452371 | GAATCACTTGAACCC[A/G]GGAGGCAGAGTTTGC | 58513 |
rs543319095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363329 | TGCCTGTCCCTCCAG[A/G]GTTGACCTTGGATCT | 58513 |
rs543327743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446574 | TTGACAGGTGGGGAA[A/T]CTGAGTTTGCCCTAC | 58513 |
rs543355875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357043 | TGGGAGCAGAAATAT[A/G]CAAACAATCCCAGAA | 58513 |
rs543376826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426314 | GCCTAGGAACACTCC[A/G]TAACTGCTGGCCTGT | 58513 |
rs543429742 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387983 | ATCCCAGAAAGAGAG[A/C/G]GGAGAGAAAATTGGG | 58513 |
rs543430347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402693 | ACTACAGGTGCGTGT[C/G]ACCACCTATATTTTT | 58513 |
rs543447206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357467 | CCCCGTGGAGGCTCC[C/T]TGGGCGAGCGAGTTG | 58513 |
rs543466379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381844 | TGCGAGTCCCCCGCG[A/G]CCTGGGATGGGGAGC | 58513 |
rs543508451 | snp | C/T | 5.04003e-05 | 0.00501972 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434496 | TTTCTTCCACCTAGT[C/T]GGAAAGAAATAGCCC | 58513 |
rs543550655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420967 | CAAGGCCCTGCTGCC[C/T]GCACCTCCCGGAGGC | 58513 |
rs543573256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400927 | AAGCTGTTCCCTGAA[C/T]GAAGACTGAGCAGGA | 58513 |
rs543581038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396834 | TGAGGAGAGGCTGCT[A/G]AGTGAAATCACAGTC | 58513 |
rs543609938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393855 | GTTACATGGCTGCCA[G/T]CCCCGGTGTATGTGG | 58513 |
rs543610147 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401208 | GGCGGTGCACCCAGC[A/G]GGGGCCAGACACAAG | 58513 |
rs543630504 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364637 | GTAAGCCAAGGCCTC[A/G]CTGCCAGGTCTCCCG | 58513 |
rs543635311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376722 | GGACAGGGAGAAGGA[C/T]GGAAGAGAAGGGGCC | 58513 |
rs543648934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458825 | CTCTACTGAACATAT[C/T]GGGCACCTTTCACTC | 58513 |
rs543672269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370349 | GTGCCCAGAGCTGCA[C/T]CCAGAGCCCCCTTCT | 58513 |
rs543708156 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371178 | GGCACATGATGGGGA[G/T]AGGTCACTGAGCCCT | 58513 |
rs543725491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408552 | GCATTCTCAGCTACT[C/T]GGGAGGCTGAGGCAG | 58513 |
rs543753379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438187 | GCGAAACCTCATTTC[C/T]ACTAAAAACATAAAA | 58513 |
rs543766399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433097 | ATTACAGGCATGAGC[C/T]GCCACACCAGCCTAA | 58513 |
rs543789262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402176 | GCCTGGTGTGAACGC[A/G]CAAAGTGGCAGCAAA | 58513 |
rs543803600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392725 | GAATTTTGTTCTGTG[C/T]AAATTATGCCACTCA | 58513 |
rs543812783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388655 | ACATGGTCAAACCCC[A/G]TCTCTACTAAAAATA | 58513 |
rs543837462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469847 | CCTTTTGCCCCCAAC[C/G]AAAAATTTTGGAATT | 58513 |
rs543843336 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389272 | CCAGCCTGGCCAACA[C/T]ATGGAAATCCCATCT | 58513 |
rs543847611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464191 | GTGCAGATGGAAATC[C/T]GAGACAAATGTCTGT | 58513 |
rs543850890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470385 | GAGCAATACTCCATC[G/T]CAAAAAAAAAAAAAT | 58513 |
rs543884284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417711 | GGCACCAGCAGTTCT[C/T]GGGCCCAGGGATAAA | 58513 |
rs543902952 | snp | C/T | 0.000708875 | 0.0188132 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385169 | AAGCCTTCAGCACTA[C/T]TGAAGGACCCACTTC | 58513 |
rs543908265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464670 | TGGCCTAGACCAGGG[A/G]TGTCCAATCTTTTGG | 58513 |
rs543945476 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436370 | TTAGAAGACAGCCCT[C/T]GTTTTTTTTCTTCTT | 58513 |
rs543957484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407113 | TTGTTTATAAGCCTC[C/T]CAGTGCATGGTGTGC | 58513 |
rs544024765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391691 | CTCTTGGGCATAATA[C/T]GCAAAATACCCGGTG | 58513 |
rs544025345 | snp | A/G | 0.000363247 | 0.0134719 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437900 | GAAGGAGTAAACAGC[A/G]TATCGCCAGTGAGGG | 58513 |
rs544047927 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448488 | TGAGCCGAGATCACA[C/T]CATTGCACCATTGCA | 58513 |
rs544049734 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414617 | TGTTGGCCAGGATAG[C/T]CTTGATCTCCTGACC | 58513 |
rs544058571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444906 | TAATTTCTGTATTTT[C/T]AGTAGAAGCGAGGTT | 58513 |
rs544063593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392169 | GGGATACCAGCTCCC[A/G]GAGAACAGACACCAT | 58513 |
rs544120024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359201 | AAAGAGTCACGCTGC[A/C]AATCTGCCGGGCAGT | 58513 |
rs544164645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423879 | CCACGGGTCCCAAGA[A/G]GAAATTACGTATGAA | 58513 |
rs544173493 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434949 | TCTTTTTTTTTTTTT[C/T]TTTCTTTTTTTGAGA | 58513 |
rs544191012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372416 | CTCTAGAACACAAGA[A/G]ATGGCACCAAAGCCA | 58513 |
rs544193530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384781 | GGACGCCTCGCACCT[G/T]CAGGCCTGCTGCCCA | 58513 |
rs544213214 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461512 | GTGTGGTCCCAGCTA[C/T]TCGGAGGGCTGAGGC | 58513 |
rs544227421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373198 | TGTCAGTCTGTCTAT[C/T]TCCACCAGCTCAAGG | 58513 |
rs544228718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460767 | TTTGCAAGAACATGC[A/G]CCTAGGCCAATCGTG | 58513 |
rs544228817 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467416 | CAGCCTCCCAAAGTG[C/G]TAGGATTACAGGCGT | 58513 |
rs544232840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374833 | ATGTAAGCACAGAGT[A/G]TGCATGCCCGGGTGT | 58513 |
rs544298702 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461424 | CTCAGGAGTTCGAAA[C/G]TGGCCTAGGCAACAT | 58513 |
rs544303442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366167 | GTGTAGCCCCCTGGG[A/T]CGGGCAGCAAGTCCA | 58513 |
rs544310196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364757 | AGGCTGTCCACTGGA[A/G]CAGAAGGGGCTCCCT | 58513 |
rs544330295 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416744 | AACAGATGCTACAGT[C/G]AGCCATGATCACACC | 58513 |
rs544371740 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383695 | CTGCTGCGCCGCCAG[C/G]GCACGCACACACGCG | 58513 |
rs544376033 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457090 | GGCCCTCCAGCAGCA[C/G]AACTCCAGCAGCCTG | 58513 |
rs544457288 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378002 | AGAGACAGTCAGAGA[C/T]AGTTATAACAATTGG | 58513 |
rs544457507 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382952 | AAAAGTTGATGATGG[C/G/T]TTTTTTTTGTTTTTT | 58513 |
rs544475517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465886 | GAAACTATGGTGCAA[A/T]GAAGAGGCCTGAACC | 58513 |
rs544579814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457763 | GGACATCACCCCTCC[C/T]GGGCATCTCAGAGAA | 58513 |
rs544607411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410093 | GAGCTGAGATTGCAC[C/T]CTTGTGCTCCAGCCT | 58513 |
rs544622969 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467176 | TTTTGAGACGTAGTG[C/T]CACTTTGTTGCCCAG | 58513 |
rs544651125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369576 | CAAATATCATTTGAA[G/T]TGAGAAATAACAATT | 58513 |
rs544689271 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424216 | ATTGCTGGCCTGGAG[A/T]TGAGGAAGTTGGAGT | 58513 |
rs544694705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407161 | TGGACTAAGACACAC[A/G]TGCCATGTCAGCGTC | 58513 |
rs544708678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363232 | CGCAGCACCCCAGAC[C/T]GGAAGCTCAATAATA | 58513 |
rs544739577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445113 | GAGTTTCAGTCTTTG[A/G]GGCATGCAGGGTTAT | 58513 |
rs544754664 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428556 | AAGACAGAAAAGAAA[A/G]GAAAAGAAAGGAAAA | 58513 |
rs544775996 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413596 | TTTATACAAGAAAAA[G/T]AAAGTGAATTCAGCC | 58513 |
rs544786872 | snp | C/T | 1.66579e-05 | 0.00288595 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402451 | CTGTGGGCCTCCTGG[C/T]GGCTTTCATGCAGCT | 58513 |
rs544789102 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472463 | GGGACCCGCACCCTG[C/T]CCCCCTCACCCTGCC | 58513 |
rs544795494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356324 | TTCTTTTTCTTTTTT[A/T]TTTTTTGAGATGGAG | 58513 |
rs544804433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463417 | CTCTTCCTGAAACAA[A/C]CTCAGGCCAGGTTCC | 58513 |
rs544822612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401310 | GGACTGAGGACTTGG[C/G]TGCTGAGAAAAGAAA | 58513 |
rs544826228 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400080 | GGTGGCTCACGCCTG[C/T]AATCCCAGCATTTGG | 58513 |
rs544837451 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439814 | GGCACAGCACAAACA[A/C]GGTCCCTTCTAACAA | 58513 |
rs544867780 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457244 | GACACCTTGGTGCAG[G/T]TGTGGAGGTGAACAA | 58513 |
rs544867819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464011 | AATGAGGACTGCAGG[C/T]CTGGGAAACACGGGG | 58513 |
rs544896471 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422336 | CTCCACCTGCATTAC[A/C]GCGGGCCTTCAATAC | 58513 |
rs544902787 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371337 | TGGGTGGATGCCACA[-/C]ACAGGTACGGGAGGG | 58513 |
rs544913127 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403970 | TAAAGAGATTCACAG[C/T]GCAGGATGAAATGGG | 58513 |
rs544946124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375748 | TCTAAATCCACACAG[C/T]CCATACTTGGTCATA | 58513 |
rs544961824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416565 | TCACTTGAGCCCAGG[A/G]GGCAGAGGCTGCAGT | 58513 |
rs544973649 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378479 | AGAGCCTGGCTGGAC[A/C]CCACTGCCGTCCCCC | 58513 |
rs544976111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414227 | GGCCCTGGCTGACCT[C/G]AGAAAGGAAAAAGAG | 58513 |
rs545010647 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407031 | TGGGTCCTCACCAGA[C/T]GCTGAATCTGCAGGC | 58513 |
rs545050496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452144 | ACTTCGTCTCAAAAA[A/C]AAAAAACCACACAAC | 58513 |
rs545080795 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381619 | GATCACACCAAGTAC[A/G]AAGCTGCGATTGGAA | 58513 |
rs545147167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438255 | CTACTTGGGAGGCTG[A/G]GGCAGGAGAATCACT | 58513 |
rs545148638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418953 | ATGGCACTTTGTCAC[A/G]GCAGCCCAATGGTCT | 58513 |
rs545150427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412052 | CTAATATAATGTAAA[C/T]GCTATGTAAATAGTT | 58513 |
rs545153169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407818 | AAATGTCATTGCTCC[A/G]TCAGGCCACAGCGCA | 58513 |
rs545172258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431964 | ACAAAATACAGTAGT[C/T]GTGGGACGTGAAACC | 58513 |
rs545184709 | in-del | -/AAAAC | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410915 | GAGACACTGCCTCTT[-/AAAAC]AAAAAATGTGCTCCA | 58513 |
rs545191110 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469705 | GGTGGAGAAAACACA[A/C]CCCTCCTCCCCTAGG | 58513 |
rs545195293 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415835 | GACAGGGGCTCCCTC[A/C]ATCCTTGGCCTGCCC | 58513 |
rs545211787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412804 | TGGGGCTGGGGTCGC[A/G]GCCGTGGACAGCACC | 58513 |
rs545248606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443081 | TAAAAGTTTACGTGC[A/G]TTGGTGTTTTAGTAA | 58513 |
rs545260686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381740 | GGGCCGTTTAGGGTC[A/G]GCTGTTTGGGAAAGA | 58513 |
rs545297182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376114 | GGAAAGGGCTCGGGG[A/G]CATGCCCTATCTAGG | 58513 |
rs545309786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443744 | ATAATAATGCCCGGA[A/T]TATGGTCAGCGTCTC | 58513 |
rs545328071 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450130 | CACATGCCTGTGGTC[A/C]CAGCTACTCAGGAGG | 58513 |
rs545357265 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409220 | TCGGCAACAGAGCGA[C/G]ACTGTCTCTAAAAAC | 58513 |
rs545367566 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364868 | GGCCGCCCACCAGCT[C/T]GGCTCCCTTCCCTGT | 58513 |
rs545383292 | in-del | -/CTGA | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359107 | GTGACCTGGGCCCCC[-/CTGA]CTGCCAGCATGGACT | 58513 |
rs545393008 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437958 | TTCAGGGAAAGAGGA[C/T]GTGCACTTCAACAAT | 58513 |
rs545452154 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454220 | ATTGCTGAGTCTCCA[G/T]GGGACAGAATAAATA | 58513 |
rs545463554 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355442 | TCGTCCCCAGAGGAA[C/G]AGCGGGAGGCAGTCA | 58513 |
rs545477324 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368628 | TCATTCACCCTACAC[A/G]ACACAGGCACCCACC | 58513 |
rs545489157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425027 | CATGTTAAGAACTCC[C/G]GAGAAACATCCTACT | 58513 |
rs545492360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428632 | GAGAGAAAGACAAAC[A/G]AATCCAGCAACCCCT | 58513 |
rs545504489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429157 | CACCCCTCCCTTGCA[A/T]TCTCAGCTGGGCAGG | 58513 |
rs545540110 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405885 | CAAAGCTGAAATAGC[A/G]CAACGGGCATTGTGA | 58513 |
rs545547478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416433 | TTGAGCTCAGGAGTT[C/T]GAGACCAGCCTGGGC | 58513 |
rs545555696 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388880 | TAAGGACAATGGAGG[C/T]TGGAAGGCAGTGGAA | 58513 |
rs545571132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455549 | GGAGAGACTGCCCAG[C/T]TCCATCTACACCTAT | 58513 |
rs545605173 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444064 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs545605180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462022 | CAGGGAGCAGGAAAG[A/C]CAGAGCTCCTCGACC | 58513 |
rs545609383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374751 | GCCCAGCAAATACGG[A/C]ACTGCTCGGCAAGTG | 58513 |
rs545650954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360046 | TGCTAAGCCAAATGA[A/T]ACCTTGAAACCTTGG | 58513 |
rs545668273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412208 | AAAAGAGAAGCCACC[A/G]TCTATGGTTATAAGC | 58513 |
rs545686343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402782 | TAGAGATGGGGTCTC[A/G]CTATGTTGTCCAGTC | 58513 |
rs545725198 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372128 | GGTCCCCAGAGTGCA[C/G/T]TTTCTGGCTTAGATG | 58513 |
rs545726959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446647 | CAGGATAGGTGGTCC[C/T]GGAGTCAGACCCTCA | 58513 |
rs545730751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399733 | TCACCCAGGCTGGAG[A/T]GCAGTGGCACGCAGC | 58513 |
rs545767475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396987 | TCATGGGGATGAAAA[C/T]GTTCTAGAGCTGGGT | 58513 |
rs545777993 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369760 | TCACAAGCCAGTCTT[C/T]ATGACAAAAATAATA | 58513 |
rs545792788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389351 | CCCAGCAACTTGGGA[C/G]GATGAGGTGGGAGAA | 58513 |
rs545830033 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382740 | TGAGCTTATGTCACA[A/T]AGGCTTGATACTGTC | 58513 |
rs545833738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390407 | GAACAATTCCACAAT[C/T]ATAGGAGAATGTTTA | 58513 |
rs545846274 | snp | C/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472741 | AGGTGGGAGGGTCAT[C/G]AGGTCAGGAGTTGGA | 58513 |
rs545870493 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432225 | GATCACCTGAGGTCA[A/G]GAGTTCAAGACTAGC | 58513 |
rs545872443 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391457 | GACCAAAAGGTCCAC[A/G]GGGAGTGAGCGAGGT | 58513 |
rs545894146 | in-del | -/TGGCC | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374216 | TCCAGGAAATGGGCA[-/TGGCC]TGGCCTGGCCTGTCT | 58513 |
rs545936497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415734 | CCTGTCACCTCCACA[C/T]TGGGGAAACAAGGCT | 58513 |
rs545971520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394564 | CTCCTGGAAATACTG[C/T]TTTGCTCTGAAACAT | 58513 |
rs546010589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395093 | GGTGCGGTGATGGGC[A/G]CTGAGGCAGGAGAAT | 58513 |
rs546038600 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465682 | GCAAGAGCCTGTCTC[-/T]AAAGGAAAAAGGAAG | 58513 |
rs546040666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447285 | GCTCCATCAGAGGTT[G/T]CTACAGCAGAGCTAA | 58513 |
rs546058848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453169 | CAGTGGTGCCATCAT[A/C]GCTCACTGCAGCCTC | 58513 |
rs546066318 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363971 | CTGCCTGTCCGCCTC[C/T]GCCCGTCCCACAGGG | 58513 |
rs546101053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364537 | CCCCGGGCTGGTTCC[A/G]CTGGCCTTGAGGAAC | 58513 |
rs546103929 | snp | A/G | 0.000461582 | 0.0151848 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440923 | ATCTGCGGAAACACA[A/G]AAATGCTCATAAGCA | 58513 |
rs546139194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358078 | AATCAAAGCCTGGAA[C/T]GACCAAGTAACCGGC | 58513 |
rs546145187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427574 | TACATACAAAGAACT[A/G]TGTCAAGACAAACAC | 58513 |
rs546179722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464914 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA | 58513 |
rs546205812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470463 | TTAGTGCTTTCTCAT[G/T]AAATGATCTTAGGTG | 58513 |
rs546208926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464802 | CTTTAAAAAATTCAC[A/G]GGTGGGCATGGTGGC | 58513 |
rs546248750 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377376 | ACCCTCTGGACTGCA[A/C]AACATGGCCCTGCTT | 58513 |
rs546265882 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360825 | GGCTCAGAAACAAAT[C/T]GGGTGCTTTCTGTGC | 58513 |
rs546273533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405264 | AGGGACCCCAGGGTC[A/G]GGGGGTGTCGCACTC | 58513 |
rs546273596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412149 | GTTAGATCCAAAGAT[A/G]CAGAACCCTTGGATA | 58513 |
rs546275038 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374440 | CTCCCTAAAAAGCCT[C/G]AACCCTGAAGCCAGG | 58513 |
rs546284407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458889 | TTAACTACAGGGATG[C/T]GTCCTGAGAGTTGCA | 58513 |
rs546325573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371272 | GCTTCCTCGGTGGCT[A/G]CATCCTGTGTGGCAC | 58513 |
rs546335034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405557 | TCTATGACAGCAAAA[C/T]CCGTAAACAATGCAG | 58513 |
rs546347091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386660 | CACTCCCAGGGGAAA[A/G]GAAGGGGAATCGGGA | 58513 |
rs546363161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401944 | TCAGATGTCCCCTGC[A/C]CCCTGATTAGTAGAA | 58513 |
rs546410519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384865 | TGGCAATGACTTCAC[A/C]GTCTGAGACCTGATG | 58513 |
rs546442079 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448570 | GGAGAAAGGCCGGGC[A/G]CGGTGGCTCACACCT | 58513 |
rs546446064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438968 | ACCCCACCTAGACAC[A/G]GGAAGGAAGTTGAAC | 58513 |
rs546491233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405602 | CTGGCTGGAAGGTTC[C/T]AGCACAGCCCACACT | 58513 |
rs546495326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466822 | ACAGGAGAATCGCTT[A/G]AATCCAGGAGGCAGA | 58513 |
rs546509507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433155 | TGTTTTGAGACAGAG[C/T]CTCGCTCTGTTGCCC | 58513 |
rs546556218 | in-del | -/T | 0.0861826 | 0.188849 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450957 | AAATGGTACAGGCTC[-/T]TTTTTTTTTTGAGAC | 58513 |
rs546571360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424017 | ATGCCAAATTGACTA[C/T]AAACCCAACACGGGG | 58513 |
rs546592795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390749 | ACTTTTAAGTAATCC[A/G]TAAGTGAACAGAATT | 58513 |
rs546604023 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376459 | GCCAAGGCTAGGAGA[-/C]ATTGGCAGCACTGGC | 58513 |
rs546608024 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460794 | CGTGTCTGGGACCCC[A/C]CAACCACAAACAGTG | 58513 |
rs546615169 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435803 | TGCAGAATCTCTCTC[A/G]ACCACAGTACACCCC | 58513 |
rs546625974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449257 | CTTAAAAAACAAACA[A/C]ACAAACAAACAAACA | 58513 |
rs546637446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358891 | CAAAAGAACCGTTCC[A/G]CTAACCTAGAAATGC | 58513 |
rs546639832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389628 | GACTACTTTTTTCCT[A/C]TTTCTTTACAATACC | 58513 |
rs546643450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442593 | TGTTCTCTGGCTCCG[A/G]AATCAGAAAAGAAGT | 58513 |
rs546693330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359649 | AAGGATCATTTGAGC[C/T]CAGAGTTCAAAGACC | 58513 |
rs546701749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424963 | ACCGCACCTGGCCAC[A/G]AGCATTTTTTAAAGA | 58513 |
rs546704649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398875 | CAGCATAGCACACTA[C/T]AGCCCAGAACTCCCG | 58513 |
rs546722627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441685 | CCCCAAAAGTACTCG[C/G]GTTTCTTATCTGCTA | 58513 |
rs546756021 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428289 | AGGCCGAGGCGGGTG[G/T]ATCACAAGGCAGGAG | 58513 |
rs546756342 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460551 | TGCCAACTCCATGGC[C/T]TGGTGTGAGCAAGCA | 58513 |
rs546782012 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459285 | GAAATAAGTCCCTCC[C/T]GCCTCCACACTCCCA | 58513 |
rs546794487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453577 | AATTAGCCCAGCGTG[C/G]TGGCAGGCGCCTGCA | 58513 |
rs546795461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379028 | TGTGTTCCTGGCCGG[A/G]CGCACTGGCTCACGC | 58513 |
rs546834194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373617 | ACTCATCTGCTGACC[A/G]CTCTTGCCCATAACC | 58513 |
rs546854137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429797 | CCACCTACTTTACCA[A/G]GGATCCAGGACTCCA | 58513 |
rs546866588 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374078 | GTTCTGAAGCTCATG[A/G]CTTGGTTCTCGTTAC | 58513 |
rs546868973 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417470 | GAGCAAACTTCCAGG[A/T]GAGCCTCTGATATTT | 58513 |
rs546877663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378160 | GACAGGGAGGCGGGT[C/G]GGTGGTAGACAGGGA | 58513 |
rs546899610 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407568 | TGGCCTCAAGTGATC[C/T]GCCAGACTCAGTCTC | 58513 |
rs546914747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372551 | CGGAAAAGATTTCCA[C/T]TAAACTGTGACCTCA | 58513 |
rs546915795 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429701 | TGGCAGATGGGGCCC[C/T]GTCACCTGGCTGCTG | 58513 |
rs546927983 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423116 | CTCCTGTGATGTCCA[A/G]ATCTAACAGGCTCCT | 58513 |
rs546942460 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397342 | TAATCCACCCCCCTC[A/G]GCCTCCCAAAGTGCT | 58513 |
rs547040833 | in-del | -/A | 0.00279162 | 0.0372561 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473189 | CAGTACGTATTCCAT[-/A]AGGAAAAGAGAAGTC | 58513 |
rs547045369 | snp | A/C/G | 0.0001977 | 0.00994056 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394045 | TAGCTCTAGGGCACA[A/C/G]GATGCGGGCCGGGCC | 58513 |
rs547061427 | snp | A/C/G | 0.00358923 | 0.042236 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434696 | CGTTATGGCAACCTC[A/C/G]GATCTGGGAGCCAAG | 58513 |
rs547061580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438023 | GGGCTGAACTGGACT[C/T]ACCTTGGGGACATCG | 58513 |
rs547089635 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411833 | GCCTCCTGAGTAACT[A/G]GGACTACAGACACAT | 58513 |
rs547115727 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369324 | ACTAAAAATATTTAC[C/G]GAATTTTGAGAAAAT | 58513 |
rs547168712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371660 | CCGCAACGCAGGGCC[A/G]CGCTGGCAGGAAGTG | 58513 |
rs547169706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450604 | TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGATT | 58513 |
rs547216474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361608 | TTTTATTGAGAAACT[A/G]TTTTTCTTACAGAAG | 58513 |
rs547232933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451076 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 58513 |
rs547263458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362021 | AAAAAGGAGAAAGAA[A/T]GAAATATGAGTTACT | 58513 |
rs547264678 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368540 | TCCCACACATCTCTC[A/G]TTCATCCTGCACAAC | 58513 |
rs547279644 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420360 | TGTCAGGGCGCTAAC[C/T]AGGAACTGTATGTGT | 58513 |
rs547297686 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409756 | CAGCCTGGCCAACAT[G/T]GTGAAACCCTGTCTC | 58513 |
rs547301069 | snp | A/G | 0.00571004 | 0.0531264 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355741 | CTTGCTGAGCGCGAT[A/G]GCCAGTTCCAGGTCC | 58513 |
rs547345909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402788 | TGGGGTCTCGCTATG[C/T]TGTCCAGTCTGGTCT | 58513 |
rs547379288 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453637 | AGAATGGCGTGAACC[C/T]GGGAGGCGGATCTTG | 58513 |
rs547482156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462491 | CATGGTGAAACCCTG[C/T]CTCTACTAAAAATAC | 58513 |
rs547504386 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356618 | CCCGGCTCTGAGGGT[C/T]AATTTCTCCCAGAAC | 58513 |
rs547527580 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375493 | GTGTGTGTGTGTGTG[C/T]GCTTCTGCTCCCATC | 58513 |
rs547538836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426461 | CAACAGGGAGAAACC[A/G]CATCTCTACTAAAAA | 58513 |
rs547560809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375842 | CCTGAGAGAAGGCCA[C/T]GGCCAGCCCAGGGGA | 58513 |
rs547566154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465113 | ACAAGAAAACCTCAT[A/G]ATGTTTTAGGAAAGT | 58513 |
rs547585162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412974 | AAGGAATCTGAGATC[A/G]TTGACTTTTGCCTGG | 58513 |
rs547596636 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368932 | GGCGGGGCACCACTC[C/T]AGCAGAGCTCATCCA | 58513 |
rs547633932 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472671 | ATAAGACAAGAACCC[A/G]CTTGTTGCCAGGTAC | 58513 |
rs547642733 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399788 | CAGCCTCCCAAAGGA[C/G]TGGGATTACAGGTGT | 58513 |
rs547643069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430791 | GATGAATGTATAAAT[A/C]TGGACACACGGGGAC | 58513 |
rs547680418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393035 | CAATAGAGTAAAACC[C/T]CATCTCTAAATAAAT | 58513 |
rs547699243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406755 | CACATCCTTCATGCA[C/T]AGAGCAGAGAATATT | 58513 |
rs547704184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431553 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 58513 |
rs547707716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424682 | TTTTTTTTTTTGAGA[C/T]AGAGTTTCGCTCTTG | 58513 |
rs547718892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436679 | TTTAATAATCCAACT[C/T]CTGACACTTAGTTGT | 58513 |
rs547721958 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439472 | CAAGATGGGAGGATT[C/G]CTTGAGCACAGGAGT | 58513 |
rs547752450 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373220 | AGCTCAAGGCTCGAC[C/T]GCCAGGCTCACAGGG | 58513 |
rs547774716 | in-del | -/GA | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375148 | ATGCATATAAGCATG[-/GA]GAGTGTGCACGGAGG | 58513 |
rs547801364 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365880 | GCTCGGCACACAGTG[A/G]GCTTCAGGAGGTCCT | 58513 |
rs547839442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463589 | GTGGCCCATGCTACT[C/G]TTCCCTCAACAGATG | 58513 |
rs547843340 | in-del | -/T | 0.190519 | 0.242821 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398994 | CATTTATTTATAAGG[-/T]TTTTTTTTTTTCAGT | 58513 |
rs547852775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453627 | CTGAAGCAGGAGAAT[A/G]GCGTGAACCCGGGAG | 58513 |
rs547948526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460105 | AACAGTGAGACCCTA[A/G]CCCTACAAAAATTAA | 58513 |
rs547990201 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417275 | GCTCTGCCCACGACC[C/T]GCCTGGGACCACACA | 58513 |
rs548038088 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400612 | AAGTATTTATTAAGA[A/T]ATAGAAACAAGCCAG | 58513 |
rs548085101 | in-del | -/TGTGTT | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369695 | GTGTGTGTGTGTGTG[-/TGTGTT]TGTGTGTGTGTGTAG | 58513 |
rs548101433 | snp | C/T | 2.06098e-05 | 0.00321006 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428727 | TCATCTCGATCCAAG[C/T]GCCCATCCTTGTCAA | 58513 |
rs548111518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393556 | TGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 58513 |
rs548119927 | in-del | -/CT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425796 | GGTGACAGAGCGAGA[-/CT]CTGTCTCTATAAAAC | 58513 |
rs548150992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385679 | TGCTACCCGCCCCAC[A/G]CAAGCTGCAGGACCA | 58513 |
rs548163472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465549 | TTAGCCAGGTGTGGT[A/G]TTGCATGCCTGTAGT | 58513 |
rs548177522 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459336 | GGACACTTCCTGAAG[C/T]TGATTTGATGGAAAA | 58513 |
rs548188929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377679 | ATGCCCTGGTGTGCC[A/G]CCTCCCCACTGAGCT | 58513 |
rs548218885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372670 | ATGGCAGAAGCCTGC[A/G]TCCCGGTCCCTGTGC | 58513 |
rs548219889 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378212 | TGCAGGTAGGTAGGT[A/G]GGTAGGCACTTCCTA | 58513 |
rs548265393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416869 | CAGGAAGTGACTGCA[C/T]TTCTTTATACCAGAC | 58513 |
rs548265747 | snp | A/G | 1.67161e-05 | 0.00289098 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402336 | CATGGCTCCAAAACT[A/G]CCCCTCTCTGCCAGG | 58513 |
rs548278380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409820 | GTGCACACCTATAAT[A/C]CCAGCTACTTGGGAG | 58513 |
rs548303515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402865 | GCTGGGATGACAGGT[G/T]TAAGGCACTGCACTG | 58513 |
rs548356973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364045 | CCAGCTGCGGGAGAT[C/T]CTTCCAGACTCCTTG | 58513 |
rs548384149 | snp | G/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473418 | GAGGCTGAGGCAGGA[G/T]AATTGCTTGAACCTG | 58513 |
rs548392668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382256 | GCTCCAGAATGCCCG[C/T]GTCATTTCCGAATCC | 58513 |
rs548420983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395756 | CAAGACCAGCCTGGC[A/C]AACATGGTGAAAACC | 58513 |
rs548425642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376920 | CCCACAGGACGGGGC[A/G]AGGGCGGGCAGGCAG | 58513 |
rs548534673 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472744 | TGGGAGGGTCATGAG[C/G]TCAGGAGTTGGAGAC | 58513 |
rs548549779 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370026 | CAAAGGGTAGGAAGG[A/C]GCCTTGCCCACATGT | 58513 |
rs548582901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452485 | CAGAGCCAGGTGTAG[C/T]GGCACTCGCCTGTAG | 58513 |
rs548591495 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365835 | TGCCAGCCAATACTG[A/C]CCCATGTCCCTGGTG | 58513 |
rs548646145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452990 | TTTTCTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 58513 |
rs548651558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405652 | TGGAACGGGATGGCG[C/T]CGTGTGCTTTGCCTT | 58513 |
rs548679912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440667 | ATAAATAAAAGATAC[A/G]CTAGCCATGAAAGAT | 58513 |
rs548701597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357584 | GCTGGGGGGACTGGG[A/C]AAGGTGCAGGAGCAG | 58513 |
rs548740309 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433548 | AGTAGAAAAGAGCCA[-/G]GGAGTGGTGGTGCTC | 58513 |
rs548743548 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449009 | CCAGGCATGGTGGTG[C/T]GTACCTGTAGTCCCA | 58513 |
rs548744333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379591 | GCATCTAGTCACACC[A/G]ATGCAGCTGACTAAG | 58513 |
rs548766207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467743 | GTGTCCGAGCCACTC[A/G]GCATTCATTCCAGAC | 58513 |
rs548778897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380075 | TAGTCACACAGATGC[A/G]GCTGCCAAAGGCTCT | 58513 |
rs548821190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374875 | CACGCACGCATATGT[A/G]TGTGCACGTTTGCAT | 58513 |
rs548834141 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458520 | CACCCACGGCCCTGC[C/G]TTCACCCGCTTCCCC | 58513 |
rs548835975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427120 | AGGAGAAAGATAAAA[C/G]AAATGTAGGAAATTA | 58513 |
rs548860938 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421133 | ACCGTCACGGAGCGC[C/G]GGCTTCGAGCCTTGG | 58513 |
rs548916525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461571 | AGGTTGCGGTGAGCT[A/G]AGATCGCGCCACTGC | 58513 |
rs548924718 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379206 | ACTACTCGGGAGGCT[A/G]AGGCAGGAGAATGGC | 58513 |
rs548927674 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473814 | AAATACAAAAATTAG[C/T]CGGTTGTGGTGGTGG | 58513 |
rs548976693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449823 | ACTCAGCAATGAAAA[G/T]GAATGAACAGCTGAC | 58513 |
rs549014187 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436791 | GCTGTGGCCACTCAC[A/G]CTGAGACAGAAGAGC | 58513 |
rs549019627 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432955 | GACTACAGTCACGCA[C/T]CACCACACCTGGCTA | 58513 |
rs549039598 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443245 | AGGACTATCTTGGGG[G/T]CAGGATTACAGTGTT | 58513 |
rs549047402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412237 | GCAACTTTAAAAACT[G/T]TAGCCTGTAATTCCA | 58513 |
rs549049259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405982 | AGGGGCCTCGGGTGG[C/G]GTCCAGGGAGAGGCA | 58513 |
rs549102951 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354831 | GTTGCAGTGAGCTGA[G/T]ATCACACCACTGCAC | 58513 |
rs549103625 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466972 | CCTGACACTCTACTG[C/T]GACAAAGCAGGTCAA | 58513 |
rs549137160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436039 | AACCCTTCACCACAG[C/T]GATTGCCACTGGCAA | 58513 |
rs549144609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447763 | AGACTTCATCTTCGG[A/G]AAAAAAAAAAAAGGC | 58513 |
rs549192918 | in-del | -/AAAAT | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396673 | AATGAATGGATAAAC[-/AAAAT]GGAAAAACAAAATTT | 58513 |
rs549193514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358522 | TTCCCTCTGGCATTA[C/T]CATGGAACCGAGACA | 58513 |
rs549202089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429965 | TTGACCCACCAGATG[C/T]CAGCAGCACTCGACC | 58513 |
rs549207838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448401 | CAGGCATGGTGGCGC[A/G]TGCCTGTAATCCCAG | 58513 |
rs549216881 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366697 | CTTTGGTAAGAGAGG[A/C]GATTTTGGACCTGAC | 58513 |
rs549230265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358976 | ACCAGAGAGGGAAGA[C/G]GTTTCCCGGGAACAG | 58513 |
rs549249129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384922 | GGAGCCCAGGGCACC[C/T]ATGCCACTGGGAAGG | 58513 |
rs549276736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418586 | GGGGTGTCATCATGA[C/T]GAAGAAAGAATCAGC | 58513 |
rs549290532 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382183 | TTGGCAACTCGCGAG[G/T]CGACAGGCTTTCAAT | 58513 |
rs549294412 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454187 | GAAACAGCAGAGGAC[A/T]GGTTAAGCTGCTAAT | 58513 |
rs549298483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373427 | TTTTTGGTTTGTTTG[C/T]TTGTTTTAAGAAAAC | 58513 |
rs549321529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391838 | TTACTCCTGCCGTGA[C/T]GGGAGCACCTACCAA | 58513 |
rs549339263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365795 | AGGGTCAGCTCTGTG[A/G]AAAGCGGGCCCAGCA | 58513 |
rs549362033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384554 | GCTGTCTGGGACCAG[A/G]GCCACAGTGAGTTCA | 58513 |
rs549373540 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390684 | TCAATAATAATAGTA[G/T]TATAATATACCTAGG | 58513 |
rs549376387 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369762 | ACAAGCCAGTCTTCA[C/T]GACAAAAATAATACA | 58513 |
rs549379346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470782 | AATTGCTGCGGTCTC[C/T]ACTCCCAAACGTCCA | 58513 |
rs549427067 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455802 | TGGTATCCTCCTCAT[C/T]GCCCTCCTTCCACTG | 58513 |
rs549428701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429548 | CCACCTCTGCTGCTG[C/T]GCCCGAGGCTCAGGC | 58513 |
rs549491511 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464828 | GTGGCTCACGCCTGT[A/C/T]ATCCCAGCACTTTGG | 58513 |
rs549544193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364856 | CATCTCCCTATCGGC[C/T]GCCCACCAGCTCGGC | 58513 |
rs549594725 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424633 | CTGAGTAACATAGGG[A/G]AGACCATGTTGAAAT | 58513 |
rs549607376 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441770 | TGAGAGGTCTGCAGC[A/G]ACCAGGCCACTACCC | 58513 |
rs549614405 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438707 | GCTAAGTTTTTATTT[A/C]TTTTTTTAGAGGTGG | 58513 |
rs549683212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444311 | CATGGAAAAGACATA[C/G]GAGGTAAGTGTGTAT | 58513 |
rs549702769 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362174 | TCCCAGGGGCTTAAC[G/T]GGTTGTGAACAACAC | 58513 |
rs549719743 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359751 | CCTGAGGTCCCAGCT[A/C]CGTGGGAGGCTGAGG | 58513 |
rs549725393 | snp | C/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398077 | ATCAAAGGTCCAAAA[C/G]AAAGTTTCCTAGCAA | 58513 |
rs549773214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433311 | TTTTGTATTTTTTTT[C/T]AGTAGAGACAGGGTT | 58513 |
rs549788157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395528 | GTTAAAGCAAAGTAC[A/G]GAATTCCATACTTAA | 58513 |
rs549821521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432911 | AGGCTCAGGTGTGAT[A/T]CTCCCACCTCAACCT | 58513 |
rs549899599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407364 | AGGCTGGAGTGCAGC[A/G]GTGCAGTCTCAGCTC | 58513 |
rs549908364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421140 | CGGAGCGCGGGCTTC[A/G]AGCCTTGGCACGTGC | 58513 |
rs549924516 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451780 | GTGATCCACCCGCCT[C/T]GGCCTGCCAGAGTGC | 58513 |
rs549925616 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393607 | TGAGCCGAGATCGCG[A/C]CACTGCACTCCAGCC | 58513 |
rs549977362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362921 | GAACTCCAGGATGCC[C/T]GGTCCCAGCAAGGTA | 58513 |
rs549994063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369817 | CTTCTTTGAAAATTC[A/G]CATTTGTTCTCTGGC | 58513 |
rs550007069 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449432 | AAACCACAGTGAGAT[A/G]CCACTGCACGCTATC | 58513 |
rs550017157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356564 | ATCCACCCGCCTCAG[C/T]CTCCCAAAGTGCTGG | 58513 |
rs550057511 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388335 | ATGAGCCACTGAACC[A/G]GCAATGAAAACTTAT | 58513 |
rs550057542 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416692 | TGCGTCCTAGCTACT[C/T]GGGAGGCTGAGGTGG | 58513 |
rs550062003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425723 | GGTGGGAGGATTGCC[C/T]GAGCCCAGGAGATGG | 58513 |
rs550094610 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414487 | CTCACTGCATCCTCC[A/G]CCTCCCCAGTTCAAG | 58513 |
rs550110215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386354 | AGAGGGAAAGTGGAA[C/T]GATTAAAACTCAACC | 58513 |
rs550129293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417410 | TGAGCCAGTTTAGGA[C/T]CTCAGAAGCTGTATC | 58513 |
rs550138917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431592 | CATGCGTGAGCCACC[A/G]TACCGGGCCAGAAGG | 58513 |
rs550148813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394856 | TGTGGGTCTTGTGGT[A/G]AGCTTGGAACACTTC | 58513 |
rs550177321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375596 | TCTGTGTAAGGCACA[A/G]GTGGCCTCTTGCAGA | 58513 |
rs550209332 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468999 | CACTCCAGCCTGGGG[A/G]ACAGAGCGAGACCCT | 58513 |
rs550216107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375951 | GAGGGTCACTCGTAA[C/G]TAGTGAGCTGGGGGC | 58513 |
rs550236463 | snp | C/T | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421449 | ATCGCATCTTGTCTG[C/T]CACGGGCACCACCCA | 58513 |
rs550247328 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380926 | TGGCTGCCTCGGACC[C/T]TGTGTAGTCCTAGAG | 58513 |
rs550288033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414285 | GGATTCTGCCAACAC[C/G]TGAATGAGCCTAGAA | 58513 |
rs550301995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378766 | ATCTCAGGCGTCTGA[A/G]GGAAGGGGCTGGGGT | 58513 |
rs550303021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411371 | AAGTTAGTGTCAAAC[G/T]CTTCCACTCACTGAA | 58513 |
rs550348050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390533 | GTAGAGCATTACACC[C/T]AACAACTAGATACAC | 58513 |
rs550367289 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458120 | CTCCTGTCGGGGTGT[A/T]CCTGACAGTGGGGGG | 58513 |
rs550367471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454998 | GCCAGGTGTGGTGGC[A/G]CACACCTGTAATCCC | 58513 |
rs550369941 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443657 | GGAGGTTGCAGTGAG[A/C]CGAGATCGTACCACT | 58513 |
rs550406002 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400458 | CAAACATAGGAAGTT[C/T]CAGATGTACCACTGT | 58513 |
rs550420010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468593 | TCAAGCAATCCATCC[A/G]CCTCAGCCTCCTAAA | 58513 |
rs550441591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432071 | ATAGGGGCCCTGGAA[C/G]CAATCCCCCTAAGTA | 58513 |
rs550456409 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405251 | CGGAGGGAACCACAG[A/G]GACCCCAGGGTCGGG | 58513 |
rs550456465 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373680 | CGTGTGGCCAGGAAC[C/G]GGGAAGGGAATTGTA | 58513 |
rs550464899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416971 | GGAGCCACAGACCTG[A/G]AGGCCCCTTCACACC | 58513 |
rs550466905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423171 | AGCAAGCTTGGGAAA[A/C]AAGGGATACCATGTG | 58513 |
rs550490982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387467 | AAAAAATTAGATGGG[C/T]GTGGTGGTGGATGCC | 58513 |
rs550495425 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403235 | AGAAGCCAGCGCCCC[A/C/T]CCCTGGACTGGGAAG | 58513 |
rs550516659 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473696 | GGGCATAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 58513 |
rs550522487 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427942 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 58513 |
rs550529420 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469362 | GAGGAGGATCGGCTG[C/G]AGCCACAGGGCACCG | 58513 |
rs550531532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462799 | CAGGACACTGGTCCA[C/T]GCAGTGTACAGCCAG | 58513 |
rs550611223 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425956 | ATCACCATTTGGCAG[C/G]CACCATCATCATAAT | 58513 |
rs550625205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448479 | AGGTTGAGGTGAGCC[A/G]AGATCACACCATTGC | 58513 |
rs550629992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373465 | CCAGCAGTTTGAAAA[C/T]GTTGGACTTTATGCT | 58513 |
rs550709670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403645 | GTAAGTAACAAGGGT[A/G]AGAGCAAAGGAGTTC | 58513 |
rs550710023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397177 | TCACTGCAACCTCCA[C/T]CTCCCGGGTTCAAGT | 58513 |
rs550710520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390057 | TAATGGACTAAACAT[C/T]ACACTTACAAGGCAG | 58513 |
rs550750731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434154 | AGGATTCTGGCACCT[C/T]CCCCAGGGACTGGGT | 58513 |
rs550761123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464985 | GCAGGAGGCTGAGGC[A/G]GTAGAATGGCATGAA | 58513 |
rs550764957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358260 | TTCAAGGCCAGCTCA[C/T]GAATCCACTGTGGAG | 58513 |
rs550776110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383780 | TCACAAGTTGCGACC[A/G]CTGCCAACCCCAAGA | 58513 |
rs550795984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370872 | GGATGGGGGGCGTGG[A/G]CAGGAAAGAGGGACT | 58513 |
rs550808979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378424 | TCTCCTGCTGGGGAA[C/T]TCGGCCCACCTCGTC | 58513 |
rs550816470 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371607 | TGGTTAGCGGTAGAA[C/G]TGCGCTGGCTGGTGT | 58513 |
rs550828106 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422655 | AAAGTCATTCCTCTC[A/G]GTTATGAAAGGATTT | 58513 |
rs550883264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458609 | GAGGCTAAGGTCCAA[C/G]CCCTGAGCCCAGTCC | 58513 |
rs550890612 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383213 | GCCCGGCACCGCCAA[C/T]AGGAAGTGAGACCGG | 58513 |
rs550920544 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359185 | AGAACGTCCACGCTG[-/A]AAAGAGTCACGCTGC | 58513 |
rs550924127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402918 | CCTGACACCCAACTA[C/T]AAACTCTAAGGGTTA | 58513 |
rs550927422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379166 | AAAAATTAGCCGGTC[A/G]TGGTGGCGGGCGCCT | 58513 |
rs550946203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364299 | TGCTGGAGACCCTTC[C/T]CTAGAGGGGCAGTGC | 58513 |
rs550968012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393657 | CCGTCTCAAAAAAAA[A/T]AAAAATAAAAAATAA | 58513 |
rs550970397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446779 | TGATGACGTGCTGGA[A/G]CATTTTATTAAACAG | 58513 |
rs550983355 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357622 | CAAGGAACCTGGTTG[A/G]GAGGCAGATGTGGCA | 58513 |
rs551006641 | snp | A/G | 5.02963e-05 | 0.00501454 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361944 | ATCGGGGGCCTCGGG[A/G]AAGTCTGCGGAACCA | 58513 |
rs551013521 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419751 | AACATTGCTGATAAA[A/T]GCCTAGTTATCCCCA | 58513 |
rs551033680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447664 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 58513 |
rs551033873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440694 | AGATGGCTCCAAGTG[C/T]TTAAAAGACCTTTAT | 58513 |
rs551045783 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441171 | ACACCCTTCTTCCCC[A/C/T]AACTAAAGTCCGCAA | 58513 |
rs551069067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434605 | CATCATCACCCTTGG[C/T]TAAAAGCACAAAATG | 58513 |
rs551071194 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394653 | GCTCTGGACAGACTC[C/T]TAAAATTATCCAGAC | 58513 |
rs551075466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443878 | GATCAGTCTGGCCAA[A/C]ATAGTGAAACCCCGT | 58513 |
rs551091082 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397420 | CTGAAAGTTAAACAA[-/T]TTTTTTTTAATCAAT | 58513 |
rs551107011 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386561 | GTTGAGTTTCCATTC[C/T]GCCAGCTACAGCAGG | 58513 |
rs551112482 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408264 | ACCCCAACAGTCCAC[A/G]GAGTCCACACAATCC | 58513 |
rs551135076 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355024 | GGCTTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 58513 |
rs551146427 | in-del | -/TTTTCT | 0.00199481 | 0.0315187 | intron-variant, cds-indel | EPS15L1 | GRCh38.p7 | 19:16356301 | ACCCTCTGAGGGTCA[-/TTTTCT]TTTTCTTTTTCTTTT | 58513 |
rs551151633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462427 | GCACTTTGGGGGGCC[A/G]AGGTGGGTGGATCAC | 58513 |
rs551151687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455846 | ATGTACCCTCTCCCC[A/G]GAAACATCCCTCCAT | 58513 |
rs551155680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374977 | GTCTCAATGAATGCA[C/T]GCACATATATAAGCA | 58513 |
rs551158557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421877 | CACATGCCAGCCTCC[C/T]TGGTCCTCCCACTCC | 58513 |
rs551163959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456571 | CTGAGGCGGGAGAAC[C/T]GCTTGAACCCAGGAG | 58513 |
rs551165254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458968 | ACAAACCTAGAAGGC[A/G]GCGCCTGCTCCACGC | 58513 |
rs551166380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369102 | CCAACACACGTCAAC[A/G]TCTTCCTCTGGCTCC | 58513 |
rs551194584 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374632 | AAAAGCAGACCCAGC[A/G]CCGGGTTTAGGTACG | 58513 |
rs551231316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453015 | CCGTGTTAGTCAGGA[C/T]GGCCTCGATCTCCTG | 58513 |
rs551317669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467169 | TTTTTTTTTTTGAGA[C/T]GTAGTGTCACTTTGT | 58513 |
rs551359765 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450452 | GGGCTGGACGGAGGC[C/T]GTGAGCCCCAGGCAT | 58513 |
rs551364359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400981 | ACAATGCCAGATGGG[A/G]AAAGTAGGAGCCGGG | 58513 |
rs551369006 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375809 | CAACCTGGGCACTGC[A/G]GGCTGGGTCCCCATC | 58513 |
rs551380910 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439222 | AGCCCTTGCAGAGTG[C/T]AGAGGATCATAAGAG | 58513 |
rs551429165 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406082 | ATGGCTGGGTGGTGG[G/T]GCTGAGTCCGAGAGC | 58513 |
rs551438167 | snp | C/T | 0.000193218 | 0.00982709 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355673 | TCTCTGGAACCCGCC[C/T]GTGCCCTGTCCCGCC | 58513 |
rs551445230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437223 | TACATGAATGCTGGT[A/G]GCAGCACTATTCACA | 58513 |
rs551455502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437984 | ACAATGAAGGCCGTC[C/G]GTGCAAAAACCCCTT | 58513 |
rs551457390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431642 | CAGCACAACAGGGGA[A/G]CTATAGCTAACAATA | 58513 |
rs551486196 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461625 | AGACTCTGTCTCAAA[A/T]AAAAGAAAGAAAGAA | 58513 |
rs551498696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467805 | CCCAGCAGGCCATCT[C/G]GAACAGCAGGGCTCT | 58513 |
rs551499727 | snp | A/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383357 | CCTCTGCTCACAGTG[A/C]GAGGAGGAAGACAGA | 58513 |
rs551512844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430768 | CAGCACGGATGCAAG[C/T]GCGCACGGATGAATG | 58513 |
rs551536598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379926 | CTAGTCACACAGACA[C/T]GGCCATCTAAGACTC | 58513 |
rs551547231 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449982 | AGAGTGGTGGTTGCC[A/G]GGGATAAGGAAGAGA | 58513 |
rs551547559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441781 | CAGCGACCAGGCCAC[C/T]ACCCAGGAGGCCGGG | 58513 |
rs551574710 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356373 | CTGGAGTGCAATGGC[A/G]CGATCTCGGCTCATT | 58513 |
rs551575326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424529 | AGCTCTGCAGACACA[C/G]GCTGGGCACGGTGGC | 58513 |
rs551584239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375407 | AAATACATGGCCGCA[C/T]GTGGGAATGTGCACA | 58513 |
rs551618773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436067 | CAAAGTGCTTGATGA[C/G]AGAGGTGACTGCATG | 58513 |
rs551634161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405698 | CACACTGCATTTGTG[C/T]GAACGGGAAGGGGAG | 58513 |
rs551670281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449135 | AAAAACTAGCCAGGC[A/G]TCGTGGTGCACACCT | 58513 |
rs551674188 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389097 | CATCTGCATTAAAAA[C/T]ACAAAAATTAACCAG | 58513 |
rs551681368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412952 | GCTATCTCTTCTCCC[A/G]CCCATCAAGGAATCT | 58513 |
rs551766038 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362756 | CTCAAGTCATCTGCC[C/T]GCCTCAGCCTCCCAA | 58513 |
rs551797808 | in-del | -/T | 0.0023933 | 0.0345097 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354890 | TGTTTCAAAAAAAAA[-/T]TTTTTTTAAGGATAA | 58513 |
rs551834807 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400915 | ACATTTAAGAGGAAG[C/T]TGTTCCCTGAACGAA | 58513 |
rs551877247 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430127 | CCACATGCCCAGACT[G/T]CTACCAGAGTCCCCC | 58513 |
rs551883926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459018 | ATTACTCCCAGGCTA[C/T]AAACCTGGGCAGCGT | 58513 |
rs552012836 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455343 | TTTTGCCAGGCTGGT[C/G]TTGAACTCCTGGCCT | 58513 |
rs552014998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440613 | ACACTTTAATCACAT[A/G]TAAGGTTACAAAACA | 58513 |
rs552015027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433406 | CAAAGTGCTGGGATT[A/G]CGGGCGTGAGCCACC | 58513 |
rs552073634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430208 | GCTGCCCTGCTCCCC[A/G]TGCTCGAGTGGGTCA | 58513 |
rs552078072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433996 | AAATAAATAAATAAA[C/T]AGACACAGACACACA | 58513 |
rs552113258 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446907 | ATAATGGCTATGTTT[C/T]TCAATGCCACTGCCA | 58513 |
rs552122763 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414344 | AGAGCCCAGCCCAGC[C/T]GACGCCTTGACCTCA | 58513 |
rs552148274 | snp | C/G/T | 1.70927e-05 | 0.00292336 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392489 | TACCAAGTGAAAGAA[C/G/T]CCAGACATAAAAGAA | 58513 |
rs552167987 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367207 | CCTGGCACCTGGTTC[A/G]ATGCCATCAATCCTA | 58513 |
rs552182628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427943 | GTGCAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 58513 |
rs552207937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427321 | GTATTACAGGTTGCG[C/T]ATCCCTTATCCAAAA | 58513 |
rs552223701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383115 | GCTGTACAAGTGTCA[C/T]GAAGGCAGCTGATGG | 58513 |
rs552230596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470885 | TAAGCGCTTTTTCAC[A/G]TGCTTAATTTTCACA | 58513 |
rs552232645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396402 | GAGTAGCCAGGACTA[C/T]AGGCGCGCACCACCA | 58513 |
rs552233170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414845 | CTCCTGAGTAGCTAG[A/G]ACCACAGGTGTGCCC | 58513 |
rs552243852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421936 | GCCAAAGTGTCCTGT[A/C]CCAGGACTCTGAAGA | 58513 |
rs552298076 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451865 | AAAACAGGCCAGGCA[C/T]GGTGGCTCACACCTG | 58513 |
rs552335014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387487 | TGGTGGATGCCTGTA[A/T]TCCCAGCTACTTGGG | 58513 |
rs552349263 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414867 | GGTGTGCCCCACCAG[A/G]CCTGGCTAATTTTTT | 58513 |
rs552356746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395607 | CAGGAGTTCGAGGCT[A/G]GCCTGGGCAACATAG | 58513 |
rs552374052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388087 | TCACTCTGTCACCCA[C/G]GCTGGAGCGCAGTGG | 58513 |
rs552395437 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357129 | GAAGGTGGGGGAAAG[A/C]AGCACACAGGAACAC | 58513 |
rs552399742 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422741 | GTGGGTGGATCACCT[A/G]AGGCCAGGAGTTTGA | 58513 |
rs552420823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401546 | GGCCCGGCCCATCCG[C/T]TCCCGGAACAGCACC | 58513 |
rs552451644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469430 | GTACAAGGAGGAAAG[A/C]GATCTGGATGCATTT | 58513 |
rs552458614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413936 | TCACCCCCACAAAAG[A/C]CCCTCTGTGTGCTGG | 58513 |
rs552494110 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468561 | ATGTTGGCCAGGCTG[G/T]TCTCGAGCTCCTGGC | 58513 |
rs552517010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381644 | TTGGAATCTGGGAGT[G/T]CCCCCATCTGCTGCC | 58513 |
rs552550892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389098 | ATCTGCATTAAAAAT[A/T]CAAAAATTAACCAGA | 58513 |
rs552556035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375983 | TGCGGAGCCTGCTAG[G/T]TCCATTCCAGGACCT | 58513 |
rs552591006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419984 | AGTCAGCGGCCATCC[A/G]GCTCTGACACCACAT | 58513 |
rs552592706 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394051 | TAGGGCACAGGATGC[A/G]GGCCGGGCCCTTGGA | 58513 |
rs552596023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457983 | CCCAACTTTCCAAAG[C/T]GTACCCCGGGCCTTC | 58513 |
rs552601563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370370 | GCCCCCTTCTGAGGC[A/G]TCTGCCCCAGCCCTC | 58513 |
rs552702475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441839 | GGCCCTGACCTGCGG[A/G]GGGAGCTGTGAGGGC | 58513 |
rs552750232 | snp | C/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472607 | TCACACCATTGCAAT[C/G]CAGCCTGGGCAACAG | 58513 |
rs552804020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432888 | GCTTATTGCAGCCTC[A/G]ACTTCCCAGGCTCAG | 58513 |
rs552819852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463772 | AAAGGTGTCCATCTC[C/T]ACCAGTGGTAACAGA | 58513 |
rs552821443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391972 | GAGATGAAGGGGCAG[C/T]GGGGGCAGATGACTA | 58513 |
rs552831678 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401454 | GGGCTCCAGGGAGGA[A/G]CCCTGGGAGAGAGGG | 58513 |
rs552843250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420655 | AATTATCCAGCAATT[A/C]TTTCCTTTTGATAGC | 58513 |
rs552846721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409998 | AATTAACCAGGTGTA[A/G]TGGCACATGCCTGTA | 58513 |
rs552857037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410381 | AGTGTTGGTGAGGCT[A/G]TGCAGAGCTGGCACC | 58513 |
rs552863843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404017 | CTTAGCCCCCATCCC[C/T]GAAACAAGCTAAGCC | 58513 |
rs552867828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412567 | TATAATCCTAACACT[C/T]TGAGAAGCCAAGACA | 58513 |
rs552870200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378449 | CTCGTCCACCAGGAA[C/T]CCCTCTCCTTGCTCA | 58513 |
rs552885601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397556 | TCATCCTTTTCTCGG[G/T]GAGTATGTACCTAGG | 58513 |
rs552906890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372845 | GGGCCTCCCTTTCCT[C/T]CAATGTCCAGAAACC | 58513 |
rs552914879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390107 | AAAAAAAAAAGCAAG[A/C]CCCAACACTATGCTA | 58513 |
rs552929297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417017 | CTAAGCCCGCTCCTC[A/G]CCATCTGAGACCCAA | 58513 |
rs552934044 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457506 | TGCCACGGGGAGGGA[A/G]GGAGGAGGCTCCACC | 58513 |
rs552953635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383327 | CCCTAGCTCAGGCTC[C/T]GCTAGCTCTCCCTCC | 58513 |
rs552972178 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380223 | TAGTCACACCAAAGC[A/G]GCCATCTAAGGCTCC | 58513 |
rs552985830 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403314 | GTGATGCTCCAGGGT[A/G]GCGCCTCCTGAACAC | 58513 |
rs552991634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358690 | ATGGCCCCGGGAGGC[A/G]CCCGGCACCTGTCCT | 58513 |
rs553040574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359077 | CGGGGCACCACCTCC[A/T]CAAGTGAGGTGCGGG | 58513 |
rs553075122 | in-del | -/TTTC | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356308 | GAGGGTCATTTTCTT[-/TTTC]TTTTTCTTTTTTTTT | 58513 |
rs553092375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384063 | CCTGGGCCATGGGCT[C/T]CAGGAGGGGGGCTGT | 58513 |
rs553098833 | in-del | -/TTTTTTTTTTTTTTT | 0.49907 | 0.0215454 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362512 | CTGAGGTTTAAGTTC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTCA | 58513 |
rs553110454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372164 | AGAACTGAGTATGTG[G/T]CCTTGAGGGCAGATG | 58513 |
rs553113689 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472915 | GGGAGGTGGAGGTTG[C/T]GGTGAGCCAAGATTG | 58513 |
rs553147202 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374362 | ACAGCAGAACAAAGA[C/T]GCAGTGGCCTGTGCC | 58513 |
rs553149898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363675 | AAATGAGAAGGAGGG[C/T]GCCAAACAAGGTGAC | 58513 |
rs553186591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357390 | GTAGCCAGGATGAAG[C/T]GTGGGGTGGGATAAG | 58513 |
rs553199704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453183 | TAGCTCACTGCAGCC[G/T]CAACCTCCTGGACTT | 58513 |
rs553210318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453775 | AGGGTGACAGGATCC[A/G]TATTCCAAACCTCAG | 58513 |
rs553224133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465722 | AGGCCTTTCCATGTC[C/G]CTCTCTACCTTTTAA | 58513 |
rs553225209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357687 | TAGCTGGCCTCAGGA[C/T]CCAGATGGGGGACAG | 58513 |
rs553228695 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419473 | AAAAAAAAAAATAAA[A/T]AAATGAGGAGCCAAC | 58513 |
rs553241555 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431116 | TGATGGGGTGCACCC[A/G]TGTTCCCAGCTACTT | 58513 |
rs553255118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365195 | TGGCCCTGGAAGACG[C/G]TGTGGGGCATGGCGG | 58513 |
rs553282683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389416 | CCAAGATCACACCAC[C/T]GCACTTCAGCCTGGG | 58513 |
rs553290309 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472152 | CTGGAGGGGCTGGGC[C/T]TGAGGCATCTGCGTC | 58513 |
rs553299489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446918 | GTTTTTCAATGCCAC[C/T]GCCAAGTTTTGCAGG | 58513 |
rs553313378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468957 | CCCAGGAGTTTGAGG[C/T]TGCAGTGAGCTATGA | 58513 |
rs553315389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386668 | GGGGAAAGGAAGGGG[A/C]ATCGGGATGGAGGGG | 58513 |
rs553334742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454406 | GGGCCATGCTTACCA[C/G]GATTTCTACGGGCCA | 58513 |
rs553352191 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381270 | GCACACAAAGGAGGC[A/G]CAGCCTGCCCACATC | 58513 |
rs553353713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465176 | ATCCTGGGCCACATG[C/T]AGCCATGGGTTGGAC | 58513 |
rs553372351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469501 | GGGGACAGGGAGACA[C/T]ACAAATCACTGAGAT | 58513 |
rs553420646 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396655 | ACTCAAATGTCCATC[A/G]ATGAATGAATGGATA | 58513 |
rs553434874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471416 | GTACGATCTGCGCCC[C/G]GTGCAGGGGTGGCGG | 58513 |
rs553448731 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360107 | AAACGAGCCCTTTGC[A/G]GGTTGGGGTCACAGG | 58513 |
rs553460934 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428897 | TATACATTTCAGGAC[C/G]AGTCCGCGAGTTCTC | 58513 |
rs553462395 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407431 | GTGCCTCAGTCTCCC[A/G]AGTAGCTGGGACTAC | 58513 |
rs553486435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402544 | ACATGTCAGAAAAGA[C/T]GCTTTTTTTTTTTAA | 58513 |
rs553495135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381707 | GGGCAGTGTCGGCCT[A/G]CAGCTTAGCTTTAAA | 58513 |
rs553525455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446349 | GCCTGGCTGCCTCCT[A/G]CCCAAACTCTCACTC | 58513 |
rs553535973 | in-del | -/A/AA | 0.306431 | 0.243548 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371762 | CCGTTTCCTGCACTT[-/A/AA]AAAAAAAAAATCTGT | 58513 |
rs553539895 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439890 | AGTATTCCTCATCCC[A/G]AATGCTTGGTATCAG | 58513 |
rs553586406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413343 | AAGCTGCTCATGATG[A/G]CTAGTATCAATGACT | 58513 |
rs553594784 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423546 | CTGCACTCCAGCCAG[G/T]GCAGCAGAGCAAGAT | 58513 |
rs553629985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375695 | GAAATGATCTCTTTA[C/T]GCATCTGTATCTGCT | 58513 |
rs553638216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400107 | TTGGGGAGGTCGAGG[C/T]GGGCAGATTGCCTGA | 58513 |
rs553638678 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398519 | AGCCAGGAGGCCCAC[A/G]TGGAAAATCTGCCTT | 58513 |
rs553666340 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456533 | GTGGTGGCGGGTACC[A/T]GTAATCTCAGCTACT | 58513 |
rs553666735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443570 | CAAAAATTAGCCAGG[C/T]GTGGTGGCATGCACC | 58513 |
rs553711303 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377466 | TGGCCTGTGGGTGAT[A/G]AGCTGCCCAACATAG | 58513 |
rs553724318 | snp | A/G | 3.29979e-05 | 0.00406175 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436968 | GCCTCTGCAGAGGGC[A/G]GTGTGACCATCAGAG | 58513 |
rs553739785 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456680 | AAACAAAAACAAAAC[-/A]AAACAAAAAATAGAG | 58513 |
rs553757488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455999 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 58513 |
rs553785068 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465480 | TTGAGGTCAGGAGTT[C/T]GAAACCAGCCTGGGC | 58513 |
rs553802344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359863 | GCGAGACTCATCTCC[A/C]AATATGTAAAAACCA | 58513 |
rs553816725 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434097 | CCAAAGCCCCAGGCA[A/G]CAATTTCACTTCTGA | 58513 |
rs553853655 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461184 | TGGCAGGCGCCTGTA[A/G]TCCCAGCTACTCAGG | 58513 |
rs553864420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463924 | ATAGCAGATGCAAAC[A/G]CCTTGAGGCAAGATG | 58513 |
rs553922795 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466555 | CCAGAAAGTGTCCAG[A/C]AAAAAGAAGATGCCA | 58513 |
rs553927855 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436890 | CAACTGCTGGAACAA[G/T]TCTATCTGAAGGAGA | 58513 |
rs553929818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436123 | CATGTCCTCTCCCTG[C/G]ACAGATACCCCCACC | 58513 |
rs553944288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457137 | ACAATGCAGACACCC[A/G]GAGAAGGAGGACATG | 58513 |
rs553990039 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430265 | CACTGGGCCAAACTG[C/T]GATTATCAGGGATGC | 58513 |
rs554062525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431154 | TGAGACAGGAGAATT[G/T]CTCGAACCAGGGAGG | 58513 |
rs554091513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467237 | CACTGCAACCTCCGC[C/T]TCCTGGGTTCAAGTG | 58513 |
rs554125594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431725 | CACAAAGAAAGGATC[A/G]GTGTTTGAGGTGATG | 58513 |
rs554128732 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448326 | ACCAGAGTTTGGGAG[C/T]TCAAGACCAGTCTGA | 58513 |
rs554147181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446523 | ACCTCTCATCCTCCC[A/G]ACAACGCTAAAGGGC | 58513 |
rs554153405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453120 | TTTATTTTTCATAGA[C/G]ACAGAGACTTGCTCT | 58513 |
rs554174589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418834 | GTGGCCGTCTACAAA[C/G]TAGGCAGTGAGCCCT | 58513 |
rs554191474 | snp | A/G | 1.75622e-05 | 0.00296324 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418153 | ACAGGCGCCGACTCA[A/G]CCTGAACCCAAGTCA | 58513 |
rs554198320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357455 | GAGCTGGGATTTCCC[C/T]GTGGAGGCTCCTTGG | 58513 |
rs554208279 | in-del | -/AGGC | 0.00755907 | 0.0610114 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378215 | GGTAGGTAGGTAGGT[-/AGGC]AGGCACTTCCTATAG | 58513 |
rs554208798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446984 | TGAGTTCCTACTTAG[A/G]AAAACATATGGATGC | 58513 |
rs554210785 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420714 | AAGGCTCTGAGCAAC[A/G]AGCTCAAAAGTGACT | 58513 |
rs554230804 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416228 | GGAAAGTCAAAGCCC[G/T]TTCCATTTTCAGCCA | 58513 |
rs554244555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411950 | GCGATCCTCCGGCCT[C/T]GGCCTCCCAAAGTGC | 58513 |
rs554265511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459048 | TGGCCCGGTACAGAA[A/G]ACTGCAGGCAACTGT | 58513 |
rs554278231 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363182 | GACACCCCTCTATCT[A/G]CCCAACGGAGTCCCT | 58513 |
rs554299106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466499 | ACGATGTCAGCCCCG[A/T]GAGGCGGCACTGCCT | 58513 |
rs554305601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412426 | AATCGCTTGAACCCA[G/T]GAGGCGGAAATTGCA | 58513 |
rs554305924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405426 | TTCTGTTTCTGAAGC[G/T]CTCTCTGACCCCGTG | 58513 |
rs554309141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392587 | GATAATGGTGGCCAG[A/G]GGACCCTGAGGAGAG | 58513 |
rs554318096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405715 | AACGGGAAGGGGAGG[C/G]TATGTGTGGTATGCA | 58513 |
rs554322600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364358 | GGCCCCTCTCCTTCC[A/G]ACAGCGCCTGCCCTC | 58513 |
rs554322933 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422978 | AAAAAAAAGGGGGGG[C/G]GGATTTCTCAAAGAG | 58513 |
rs554370125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427417 | CTGGTTCAGCATTAC[C/T]AATCCAAAAATCCAA | 58513 |
rs554392879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423653 | CCTGATTTTTACTTG[C/T]GGCATTGTACTGTGT | 58513 |
rs554412099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379261 | AGTGAGCTGAGATCC[C/T]GCCACAGCAGCACTC | 58513 |
rs554412133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385053 | TGACATGAACAATTA[C/T]GCCTGGCAGCCCACA | 58513 |
rs554430695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464627 | CTGGCTCAGTCCTCT[C/T]TGCCTCCGTGTGAAA | 58513 |
rs554452884 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355488 | GCACAGTGGAGAGAC[-/G]GACCTGCAGAAGTGG | 58513 |
rs554492433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420942 | TGCCAGGCCACTCTG[C/T]TAGAGGCTCCAAGGC | 58513 |
rs554513667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408527 | TAGCTGGGTGTGGGG[G/T]CACGCATCTGCATTC | 58513 |
rs554530225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371042 | TCTCTCTGAGATCAT[C/T]GTGGGAACGAAATTG | 58513 |
rs554566540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363735 | TCAGTGTCCTGCACC[A/G]CCGTGCCCAGCATAG | 58513 |
rs554610770 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398609 | CCTGGATAAAGCAGC[A/G]AGTTAAGAATGCCAG | 58513 |
rs554618897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394386 | CTGGGCTGTCCCTCA[A/C]TTTATCACCGGCCCT | 58513 |
rs554656449 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426802 | ACATTTTTGGGACAA[C/G]TGATAAAATCTGAGT | 58513 |
rs554657194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363114 | GAGGTCCCACCTGAC[A/G]GGCCTTCCAGCATCT | 58513 |
rs554717980 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452891 | AAGCTCCGCCTCCCC[A/G]GTTCATGCCATTCTC | 58513 |
rs554718731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392553 | CTAGAAAGGTAAGAA[C/T]GCTAGTGACGGAAAA | 58513 |
rs554730175 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395770 | CCAACATGGTGAAAA[C/T]CTGTCTCTACTAAAA | 58513 |
rs554741750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403195 | CCCACAGGAGAGCAG[C/G]GAAGGGCAACGGCTG | 58513 |
rs554767904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471008 | GGGGCTGGAGCCAAG[A/G]TTTGAACACATGATC | 58513 |
rs554770044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382168 | AACCCACGAGGCCAA[C/T]TGGCAACTCGCGAGG | 58513 |
rs554805165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382655 | GCAGAAGAGGGTGAA[A/G]TAAGTTGGACTCTTG | 58513 |
rs554842330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407032 | GGGTCCTCACCAGAC[A/G]CTGAATCTGCAGGCC | 58513 |
rs554845155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368783 | ACACAACACAGACAC[A/C]TATGCAACTGTCATT | 58513 |
rs554856429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401195 | GAGGAAAGAGGGAGG[C/T]GGTGCACCCAGCGGG | 58513 |
rs554883748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458709 | ACACTCAGCCACACA[A/C]ACATACACACAATCA | 58513 |
rs554981158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445680 | AAAGGAAGATTCACA[A/G]CTACTGGGAAAGAGC | 58513 |
rs554983381 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415125 | GTGTGAGCCACAAGG[C/T]CCAGGGTTTAGTGCC | 58513 |
rs555003180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433057 | CTCAAGTAATCTGCC[C/T]GCCCCAGCCTCCCAA | 58513 |
rs555030065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356694 | TATCCGTGGGGTGTT[C/T]TTCTAAAATGTTCAG | 58513 |
rs555086987 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389122 | AACCAGAAATCGCTT[A/G]AACTTGGGAGGCGGA | 58513 |
rs555119920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376040 | GGCCAGTGGCAGATT[C/T]CAGGGGAGGGGCACG | 58513 |
rs555120950 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373665 | CACGTGGGTCTGTGC[C/G]GTGTGGCCAGGAACC | 58513 |
rs555142019 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457652 | GCCCGGGCAGGAGGG[C/G]AACAGATTCCAGCCC | 58513 |
rs555158458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369365 | CATTGAAGGGAACAG[G/T]ATGAGGTTTGGTTCT | 58513 |
rs555181133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414075 | CCCTCTAAAAGCAGC[A/G]CGCTTTCTCCACCTG | 58513 |
rs555202845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374689 | TGAAACACTGAAAAT[A/G]AAGCTTTGCACCTGT | 58513 |
rs555218908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404465 | CACGTGGTGTTTGGA[A/G]GAACTCTATTGACCC | 58513 |
rs555219097 | snp | A/G | 9.91129e-05 | 0.00703894 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385114 | AGGCGCGGGGGCTCC[A/G]TGGAGGGGCTTTACC | 58513 |
rs555235900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410534 | CAAACAGGTGTTCAC[A/C]CAAAAACTTGCAGAC | 58513 |
rs555258131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435651 | TGAGCGCTGCAGGTC[C/T]TTCTCGGGGGCCTGG | 58513 |
rs555269167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452061 | GGAGAAATGCTTAAA[C/T]CCAGGAGGCGTAGGT | 58513 |
rs555269289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444873 | CTGGGACTACAGGTG[C/T]GTGCCACCATGCCCA | 58513 |
rs555270502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454491 | AGCTGCTTTTGTAAA[A/T]TAGACAGAAATAGAA | 58513 |
rs555290530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366114 | CAGAGGAAACAGTTA[A/G]GTGTTTCCAGGGGAG | 58513 |
rs555302989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465805 | AACTAGGTATAAAAA[C/T]AAATGAGGTTAGGAG | 58513 |
rs555317936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392155 | AATGAAATCAGCCTG[A/G]GATACCAGCTCCCGG | 58513 |
rs555334069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359718 | CATTTTAAAATTAGC[C/G]AGATGTGGTGGTGCG | 58513 |
rs555379741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442712 | TCCTCCAGCTACCTG[A/G]GTGCTCAGAGACGCA | 58513 |
rs555397445 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377660 | TGGCTGTGGTGCTTG[G/T]CACATGCCCTGGTGT | 58513 |
rs555422595 | snp | A/T | 1.66255e-05 | 0.00288314 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403905 | TCAGATTCCTGAGAT[A/T]GGATTTGCGTTTTCA | 58513 |
rs555441534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384106 | GCTACTGCCTCTTCC[C/T]GCAGCGTGGATAATG | 58513 |
rs555483396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373012 | CTCTGGGTGCCCTGG[A/G]ATGGACAAACCCTGG | 58513 |
rs555492374 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391294 | GCCAAAAGCTGGTTA[C/T]GGGAAAGGTCAATGA | 58513 |
rs555514780 | in-del | -/AGGTC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395729 | CAGGTGGATCACCTG[-/AGGTC]AGGAGTTCAAGACCA | 58513 |
rs555519611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365266 | GTGTCCCCCCAACAA[C/T]TGTTCATACGTTCAA | 58513 |
rs555532960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357839 | CCCGCCATTGTGTCA[C/T]TGCCAGGGGCACAGA | 58513 |
rs555540859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467341 | TTTTAGTAGAGATGA[A/G]GTTTCACCATGTTGG | 58513 |
rs555617312 | snp | C/T | 0.000799201 | 0.019974 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460336 | CAGCTGTCATTTTCT[C/T]AAAAAAAATACAATT | 58513 |
rs555656851 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460828 | TTTGTAGGGTGTGGG[A/G]GGAATTGAGGGGGAC | 58513 |
rs555665294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449348 | TTACCAAAGAGGAAA[C/T]ATAGCAGATGGCAAA | 58513 |
rs555725273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441268 | CTGAGGTCAGGAGTG[C/T]GAGACCAGTCTGGCT | 58513 |
rs555754130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464431 | ACTGGCCACTCTCTC[A/G]GCAAGCAGACATCCT | 58513 |
rs555755475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459581 | GAGGACAAGCCACCA[A/C]GCCACCCTGGGCCTC | 58513 |
rs555777238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380594 | AGTCACACAGACGCA[A/G]CCATCTAAGGCTCTA | 58513 |
rs555799152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376548 | TGCCTGGGCAAGCTG[C/G]GGCAGAGGGGAGCCC | 58513 |
rs555813094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390991 | AACCCATCACAAAGC[A/G]AAAAATCAGAAGTCA | 58513 |
rs555822546 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422837 | GTGGTAGGCACCTGT[A/G]ATCCCAGCTACTCAG | 58513 |
rs555831217 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410052 | GGCACGAAAATCATT[G/T]GAACCCAGGAGGCGG | 58513 |
rs555856932 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406942 | TGGCCTTATAAAAGA[A/G]GCCCCTGAGAGCTGC | 58513 |
rs555866374 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453887 | AAAAAGAATTCCTAT[A/T]AAAAAAAAAAAAAGG | 58513 |
rs555900407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457723 | GCCTCTGAGCAGCCC[G/T]CCCAGCTGCTGACCT | 58513 |
rs555905178 | snp | C/T | 3.30693e-05 | 0.00406615 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440784 | GACAGTGGAGGAATG[C/T]GGAAGGAGCCGTGGA | 58513 |
rs555934009 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355297 | CTTCATTTTATACAA[C/T]GAGTGCATACACCAC | 58513 |
rs555964597 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434309 | AAAGAGAACAGTGGC[A/G/T]CCCACACACAGCAGG | 58513 |
rs555976298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414198 | AACAGGGGCAGTGTC[C/T]AGGAGCATGGAGTGG | 58513 |
rs556021242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451473 | TATGTAAAGGAAAAC[A/G]GTCTTAACTGTTAGA | 58513 |
rs556053500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428873 | CTGGGCTCAGGAGAC[A/G]GCAGTCAATATACAT | 58513 |
rs556062007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437408 | ACCATGTTAGAGAAT[G/T]CCATTGATAGGAAAT | 58513 |
rs556071235 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458864 | GGCACAAGATGCAGT[C/G]ATGCATCGTTTAACT | 58513 |
rs556073063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383418 | TGCGACAACCAGAAA[C/T]GACCAGGACGCCTGA | 58513 |
rs556076783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469683 | GAAAAGTGCAGACAG[G/T]AGTGGGGGTGGAGAA | 58513 |
rs556095735 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448251 | AAGAGCCATGTAAGG[C/T]CTGGCGTGGTGGTTC | 58513 |
rs556096844 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386775 | AGCCTGGGGGGACTC[C/G]AGGCAGCCTGTAGCT | 58513 |
rs556121584 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434859 | AGCCCACTTGTACCA[A/G]AAAGACAAAAGTGTG | 58513 |
rs556123501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431824 | ACACTACAACTATTA[C/T]GTATCATCAAAAATA | 58513 |
rs556126040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450083 | ACAAGACCCTATCTC[C/T]ACAAAAAAAAAAAAA | 58513 |
rs556168376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443749 | AATGCCCGGATTATG[A/G]TCAGCGTCTCTGGGG | 58513 |
rs556193793 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469927 | GCTAGACAGTAAGGG[C/T]CTGGGAGGGCCATGC | 58513 |
rs556197497 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409025 | CCAGGTGTTTGAGAT[A/G]AGCCTGAGCAATACA | 58513 |
rs556249943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405836 | CCTGATTTTCAACCA[C/T]GCAAATGCATTATCT | 58513 |
rs556251327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458089 | CTGCCCAGGACTCGG[A/T]TGGGATGGGTCTGGC | 58513 |
rs556297889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414517 | GCGATTCTCCTGCCT[C/T]AGCCTCCCTAGTAGC | 58513 |
rs556310771 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444916 | ATTTTCAGTAGAAGC[A/G]AGGTTTCACCATATT | 58513 |
rs556369096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418191 | CTTGCTTTTCAAAAA[C/T]GACAGCGACGAAAAC | 58513 |
rs556369192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424723 | TGGAGTGCAGTGGCG[C/T]GCTCTCAGCTCACTG | 58513 |
rs556376038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432481 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCAGGA | 58513 |
rs556431865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418904 | TCCACCCCCCAGAGC[C/T]GTGAGAAATGTCTGT | 58513 |
rs556437705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426073 | AGGCGTGCCCCACAT[A/G]AGATGAACTGAGCAC | 58513 |
rs556451014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425549 | CACAGAAAGAATCCA[A/G]TCAAGCCAGACTCCA | 58513 |
rs556454977 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417688 | CAACCTGACATCACC[C/T]GACAGGAGGCACCAG | 58513 |
rs556457202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389496 | CAGTCGACCTGAGCT[A/G]TAAGAAGTGCTAAAG | 58513 |
rs556470854 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384806 | TGCCCATGGCCCTCT[C/T]GAGACGCCTGTGCCC | 58513 |
rs556494241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461912 | AGAGACAGACTGCGC[C/T]CCTGGCTGCTGTTCC | 58513 |
rs556507280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463946 | GGCAAGATGAAGGAT[C/T]GCCTGCGCAGATGAC | 58513 |
rs556548628 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16440867 | GTGTATATACCTGTT[C/T]GTCCAAGAACCCTTT | 58513 |
rs556598877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406454 | GTGAGGTGTCCAGTG[C/G]GGGGCACAGAGAGAG | 58513 |
rs556599438 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398740 | CCACTACTGAGCAGC[A/G]TGGGAGTTTTGACCT | 58513 |
rs556604596 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456195 | ACAAGAGGAAAACCC[C/T]GTCTCAAACAAACAA | 58513 |
rs556614404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441296 | GCTAACACAGTGAAA[C/G]CCCGTCCCTACTAAA | 58513 |
rs556651278 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409963 | AAAAAAAAAAAAAAA[A/T]TCAGCTATAAAAAGA | 58513 |
rs556662552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437387 | GAGAGAGGCCAGACA[C/T]AAAAGACCATGTTAG | 58513 |
rs556668741 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461383 | CCCAGCACTTTCGGA[A/G]GCCGAGGCAGGTGGA | 58513 |
rs556703259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385736 | GGGTGTCCACAGATG[C/T]TCCCATTGCATAAAG | 58513 |
rs556730144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400519 | CCAACTTCGACCCAC[A/C]AGGGAGAACTAAGAC | 58513 |
rs556746787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468054 | AGTCTCTCCTCATCA[A/C]TGAGCCCAGTTACCA | 58513 |
rs556760258 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368590 | TTATTCATTCCACAC[A/C]ACAGGTGGTGCCCAC | 58513 |
rs556767988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422173 | GGGGCTGGGTCACCC[A/G]CTGCACGTGCGACCC | 58513 |
rs556818190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374724 | TGTTGAGTGGGATGG[C/T]TCCTCCTCAGGGCCC | 58513 |
rs556818203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380333 | CTAATCACACAGACG[G/T]GGTCATTTAAGGCTC | 58513 |
rs556831305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416385 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 58513 |
rs556865695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383296 | GGACAGGCAGAGGGC[A/G]GTCATTAGATCCCGG | 58513 |
rs556901484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421554 | TTTTGATGATGGGGC[A/G]ATTAAAGCACTTCCA | 58513 |
rs556950463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358043 | GGGTGGGAGCTGACA[A/G]TAATGTTCGCCTGGA | 58513 |
rs557030276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365034 | CAAACCCAGGGCTTC[G/T]TTCCTGGCTATGCCT | 58513 |
rs557043469 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388690 | AAATTAGCTGGGCAT[A/G]GTGGCGGGCGCCTGT | 58513 |
rs557051702 | snp | C/T | 1.69026e-05 | 0.00290706 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421304 | CAGCCACAACTGCCA[C/T]CTGTCCGGCCTTACC | 58513 |
rs557059148 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416535 | CTCAGCTTCCTGGGA[-/G]GGTGAGTGGGAAGAT | 58513 |
rs557063367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433114 | CCACACCAGCCTAAA[C/T]TGAGGGTTTTTTTTG | 58513 |
rs557087422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396847 | CTGAGTGAAATCACA[A/G]TCACAAAACAACACA | 58513 |
rs557093971 | in-del | -/T | 0.428182 | 0.17536 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439925 | GTTTCAGATTTCAGA[-/T]TTTTTTTTTTTTTTT | 58513 |
rs557168378 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384633 | CAGCCTCGCTGCTGT[C/T]CTCCTTCAACAGTTC | 58513 |
rs557190473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428061 | CAAAAATGAGGTGGG[A/C]ATAGTGGCAGGTGCC | 58513 |
rs557208322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459144 | AGCAGTATAATCTTA[C/T]GGGAGCACTGTCACA | 58513 |
rs557227360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409207 | CTGCACTCCAGCCTC[A/G]GCAACAGAGCGAGAC | 58513 |
rs557247680 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358538 | CATGGAACCGAGACA[A/C]CGTAGGGGCATGACA | 58513 |
rs557250043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453150 | TGTCACCCAGGCTAG[A/G]GTACAGTGGTGCCAT | 58513 |
rs557264835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395003 | GGCGGGTGGATTACC[C/T]GAGGTCAAGAGTTCG | 58513 |
rs557267688 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362597 | GGTGCAATCATGGCT[C/T]ATTGCGGCCTTGGCC | 58513 |
rs557299789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393450 | GTCAAGAGTGTGAGA[C/T]GAGCCTGGCTAACAC | 58513 |
rs557373977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433653 | ACACAGTGAGACCCC[A/G]TCTCTAAAAACTCAA | 58513 |
rs557376888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357200 | CAACCTGGGGGTGGG[C/T]CCGCTGTCATCTCAT | 58513 |
rs557378557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427510 | ATCTTGAAGCATTCT[A/G]GTTTCAGACTTTCAG | 58513 |
rs557402959 | snp | C/T | 3.29946e-05 | 0.00406155 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402407 | CACCATGGGCTCCAT[C/T]GAGCACCTGGTCATA | 58513 |
rs557403279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471214 | TGTCTGGAAGAATGC[A/T]GCGCTCCCAGCACCT | 58513 |
rs557412138 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393233 | GGTCTCCTTTTGGGG[A/G]GATGAGAATGTTGTG | 58513 |
rs557451191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418963 | GTCACAGCAGCCCAA[C/T]GGTCTAAAACACTCC | 58513 |
rs557462618 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360658 | AGGCCAAGACAGGAG[G/T]ATCGCTTGAGCCCAG | 58513 |
rs557521250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463433 | CTCAGGCCAGGTTCC[C/T]CTTGATCACTTCATG | 58513 |
rs557524990 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367017 | AGCAAAAGCTGCCAC[A/G]CGCACCCACGCCAGG | 58513 |
rs557525639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424808 | TGGGATTACAGGTGC[A/G]CACCACCACACCCAG | 58513 |
rs557546154 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468084 | ACGCGCTTCCTAGGT[A/T]CAGCGGTCACAAAAG | 58513 |
rs557599608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445792 | CAGCAGAGAGGGGAC[A/G]CACCAGGGGATGAGG | 58513 |
rs557601314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356855 | AATGTCCCAGACTTC[C/T]CTGAGAGGTCACTGG | 58513 |
rs557629819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401710 | AATGTAAGGGGCCGA[C/T]AGTCCCCTGCCCCAG | 58513 |
rs557660773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438936 | ATCCCCTGCCCACCC[C/T]CAGTGGCCTGACGTG | 58513 |
rs557661089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446258 | TCAGGATTGTGTTCT[A/C]ACGACTCCTAAGCAG | 58513 |
rs557663306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392755 | AATAAAATTGACTTT[A/G]AAAATAATAATATCC | 58513 |
rs557665898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449442 | GAGATGCCACTGCAC[A/G]CTATCAGAGTGGCTA | 58513 |
rs557700993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359781 | GTGGGACGATTGCTT[C/G]AGCCCAGGAGGTCAA | 58513 |
rs557723504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430412 | CACCCTTCCACAACT[A/G]TGCAACCAAGGTGAC | 58513 |
rs557773485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436861 | ACTAGAACAATTCCA[A/G]AACAATTCTAGAACA | 58513 |
rs557790283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366187 | CAGCAAGTCCAGGGT[A/G]GACACTGCTTGATTT | 58513 |
rs557792159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374633 | AAAGCAGACCCAGCG[C/T]CGGGTTTAGGTACGT | 58513 |
rs557848586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379173 | AGCCGGTCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 58513 |
rs557856445 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408597 | CCCAGGAGGTAGTGG[C/T]TGCAGTGAGCCGAGA | 58513 |
rs557929999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359305 | AAGTTAGCACAAATA[A/G]TCAAGATCCAGTGAA | 58513 |
rs557994180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442754 | CCGCGCCCGGAGAGC[A/G]CTGGCCAGTAACTGT | 58513 |
rs557998538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455326 | TTGGGGGGGTCTCAT[C/T]ATTTTGCCAGGCTGG | 58513 |
rs558011199 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465933 | TGTCTGCCTGAGCTC[A/T]CTGGGTACAAACTTG | 58513 |
rs558056090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443451 | CAGTGGCTCACGCCT[A/G]TAATCCCAGTACTTT | 58513 |
rs558058105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436242 | TTATTCATGTCAGGA[C/T]TTAAGCCACATAAAC | 58513 |
rs558146585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458684 | ACTCCACACACACAC[A/T]CACTCACACACACTC | 58513 |
rs558149296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454685 | GTAAGGCCTACAGTC[A/G]CTGCCCTGGAGAGGA | 58513 |
rs558152578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370242 | TTTTGCAGTTAGCAG[C/T]GGCAGGCAAGGGGCG | 58513 |
rs558189596 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423579 | TGTCTCTTATATATT[A/T]AAAAAAAAAAAATCT | 58513 |
rs558232064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445327 | GACCTACAGCTGAGG[A/G]AAAGCCCAGGGAGTA | 58513 |
rs558235181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457219 | AGGTGGAAATCTAAT[G/T]GCCATTCTAGACACC | 58513 |
rs558262939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452648 | GAAAAAAAAAAAAAA[A/C]AAACCTAAGAACTAA | 58513 |
rs558265882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448758 | CTGCTTGAACCCAGC[A/G]GGCAGAGGCTGCAGT | 58513 |
rs558300150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421195 | AGGGAGAATAAAGGA[C/T]GCCAGACACAGCGGA | 58513 |
rs558307690 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449627 | CATGAAACTACCGCA[A/T]GAACCAGCAACTGTC | 58513 |
rs558328830 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370905 | ACCTGGTTGGCCGTT[G/T]TAGGCTCCTTGGGAC | 58513 |
rs558378714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429104 | GTACAGGTGTTGCCC[G/T]AAACACCCACACTCC | 58513 |
rs558380000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432952 | TGGGACTACAGTCAC[A/G]CACCACCACACCTGG | 58513 |
rs558388911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422937 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 58513 |
rs558426188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469800 | GTCACCTAAATCCAA[C/T]CAGATCACAGCCACC | 58513 |
rs558436835 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394883 | CTTCCCACTGTATCT[G/T]GATGCCTTGGCTCTC | 58513 |
rs558453156 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374889 | TGTGTGCACGTTTGC[A/G]TGCATGCATTATGCA | 58513 |
rs558476301 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433302 | TGGCTAATTTTTGTA[-/T]TTTTTTTTTAGTAGA | 58513 |
rs558476696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378592 | AGGCCTCTCCCACCT[A/G]GAGGGCAAGCACAGT | 58513 |
rs558491472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406944 | GCCTTATAAAAGAGG[C/T]CCCTGAGAGCTGCCT | 58513 |
rs558520467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426178 | GGCAGTAAGAAGACA[C/T]GTTGACATCACGTTC | 58513 |
rs558522735 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395108 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 58513 |
rs558526861 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363638 | CTCCCAGCTGGCCTC[C/T]GTTTCCTTATCTGTG | 58513 |
rs558578665 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385348 | TAGACACGTGTGTCT[A/G]CATGAAGGCCTCTCA | 58513 |
rs558619333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376166 | TGATCCTGGGAGTGC[A/G]TGGGTCTCCTGTGGC | 58513 |
rs558619359 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420124 | CCCGCCCCAGCCACT[C/G/T]GCAGACACATCTAGA | 58513 |
rs558635642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400715 | TCCATGTAACGTATC[C/T]TAATCTACATTCCCA | 58513 |
rs558658126 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409523 | CAACTTGTGCTTCAA[A/G]AGACACCATCAAGAA | 58513 |
rs558681524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415290 | GCAGCCTCCAGAACT[A/G]TGCGAAATGTCTGAT | 58513 |
rs558717136 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355444 | GTCCCCAGAGGAAGA[A/G]CGGGAGGCAGTCAGC | 58513 |
rs558747827 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372699 | CCGCAGGGTGGGGAT[-/G]GGGGGCTACAGACCA | 58513 |
rs558750242 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388602 | GGAGGCCAAGGCAGG[A/C]AGATCACGAGGTCAG | 58513 |
rs558773666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426689 | CCACGTCAAGAGACA[C/T]GAAGAGCGATGGAGG | 58513 |
rs558825273 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375726 | CAACAGTTCACAGAA[A/T]ATCTGCTCTAAATCC | 58513 |
rs558834048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420836 | CGACTGGGCTCTGAG[A/G]CACTGACAGGGTCTC | 58513 |
rs558853593 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358415 | ACCTTCTAGTTCTCG[C/T]ATCTGGGTGGGTCAC | 58513 |
rs558860143 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357087 | AAGGACCCAGGCTCT[C/T]GAGGAGGGCCCTGCA | 58513 |
rs558870276 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466798 | ATCCCAGCTACTCAG[A/G]AGGCTGAGACAGGAG | 58513 |
rs558901606 | snp | A/G | 3.42346e-05 | 0.00413716 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434526 | CGAGTAAGTAGGAGA[A/G]CACACCTGTGTGAAT | 58513 |
rs558903348 | in-del | -/A | 0.00199561 | 0.0315249 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460336 | AGCTGTCATTTTCTT[-/A]AAAAAAAATACAATT | 58513 |
rs558939713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382106 | CCCTCCAGGCTGACC[C/G]GGGACACCTCGGGCC | 58513 |
rs558964966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428649 | ATCCAGCAACCCCTG[C/T]GCACTGCACATTTCC | 58513 |
rs558965041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434989 | TGCTCTGTTGCCCAG[A/G]CTGGAGTGTAGTGGC | 58513 |
rs558977059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429166 | CTTGCATTCTCAGCT[G/T]GGCAGGGCTGCGAGC | 58513 |
rs558982688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356032 | GAGCCTGTCTCAGGC[C/T]CCCCATCTGGAAAGC | 58513 |
rs558990333 | snp | C/G | 2.07132e-05 | 0.0032181 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361780 | AGGACTCAACTTACA[C/G]AGGTGAAGTCTGCAA | 58513 |
rs559002289 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416482 | CTCTACAAAAAATAT[A/T]AAAAAATTAGCCAGG | 58513 |
rs559003147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401163 | TCATTACGAGTCCAC[A/G]AGAAAAGAGAGTATG | 58513 |
rs559047958 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412102 | TCAATTTGGATTATT[C/T]TTTATTTTTTTATTT | 58513 |
rs559070278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459307 | ACACTCCCATAGCCC[C/T]AAACTTTGACAAGGG | 58513 |
rs559087038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393749 | TCCAGGGTGGGGTGC[A/G]GGCAGTGACTGGACC | 58513 |
rs559124287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394287 | GAAGACACAGAGTGG[C/G]CTAGAATTCACTCCT | 58513 |
rs559130822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375632 | GGGAGTCCCTTTGTT[A/G]TTTTGTTTTTCCTCC | 58513 |
rs559148505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462949 | TTCATCCCACCGCTG[C/T]GGGTGCCACCTGACT | 58513 |
rs559150340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456359 | AAAAGTGTGTAGGAC[A/G]GAGTCCTGGGCTTCA | 58513 |
rs559158559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409283 | GTGCCATGACAACTA[A/G]ATGTCCACATGCAAA | 58513 |
rs559177133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369815 | GGCTTCTTTGAAAAT[A/T]CGCATTTGTTCTCTG | 58513 |
rs559212576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457094 | CTCCAGCAGCAGAAC[G/T]CCAGCAGCCTGGGGA | 58513 |
rs559217050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368089 | GATGAGAGATACATA[C/G]AAAAACAAAAAGAAA | 58513 |
rs559232092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466031 | TCTTGCTCTGTCACC[A/C]AGGCTGGAGTACAGT | 58513 |
rs559238869 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455403 | AGTGCTGGGATTACA[G/T]GCATGAGCACCAAAC | 58513 |
rs559240843 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390305 | AAGGTTGTTGTGTCA[A/G]AAAGACACAACAATC | 58513 |
rs559257582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368706 | CCTACATAACACAGA[C/T]ACCCACCTAACTGTC | 58513 |
rs559278595 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399261 | ACAGAATCAGAGTGG[G/T]AAACGAGATTTCCCT | 58513 |
rs559287576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447473 | TAGTAATTTAAGTAT[C/T]ACAGGGCCAGGCACT | 58513 |
rs559351873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422433 | TTTTTTAAATATTTA[C/T]ACAAATCACTCCTTT | 58513 |
rs559353403 | snp | C/T | 4.94694e-05 | 0.00497316 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440929 | GGAAACACAAAAATG[C/T]TCATAAGCATGACTG | 58513 |
rs559370325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414894 | TTTTATTTTTTGTAG[C/T]CGAGGTCTCAATATA | 58513 |
rs559379189 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467350 | AGATGAGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 58513 |
rs559384354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415784 | ACTGGGGTGATTCAC[A/G]CCCCAGCGTCCCTTC | 58513 |
rs559387685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391490 | GCGCCAGGGTAGCAG[A/G]AGCCCTGAGAAGGAG | 58513 |
rs559412230 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416776 | CTACGCTCCAGCTTG[C/G]GTGACAGAGCGAGAC | 58513 |
rs559430249 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378192 | GCAGATATGTGGCGA[C/T]GTCTTGCAGGTAGGT | 58513 |
rs559443974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464936 | TACAAAAAATTAGCC[A/G]GGTGTGGTGGCGGGT | 58513 |
rs559445188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408619 | GAGCCGAGATTGCGC[C/T]ACTGCACTCCAGCCT | 58513 |
rs559475928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388219 | GGCTAATTTTTGTAT[C/T]AGTAGAGACGGGGTT | 58513 |
rs559477181 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473326 | CAGCCTGGCCAACAT[A/G]GAGAAACCCCATCTT | 58513 |
rs559478865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383664 | ACACACACCCTGCCT[C/T]GGTCAGAAGTGGGAT | 58513 |
rs559488935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377395 | ATGGCCCTGCTTGGA[C/T]GTGGGGTCTCTTTCA | 58513 |
rs559491578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446684 | GTGCACCCTGTAATG[A/G]CAGCCCAGGTGTCAC | 58513 |
rs559502152 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440645 | TAAAAGAAAAATAAA[A/T]AAATAAATAAATAAA | 58513 |
rs559504553 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365980 | CCTGGGGAGCGAGAA[A/G]GGAATAAAGGCATCT | 58513 |
rs559515919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, stop-lost | EPS15L1 | GRCh38.p7 | 19:16384272 | CATCTGCTTTCCTTC[A/G]TTCCTGCCAAAGAAA | 58513 |
rs559535680 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421629 | GGCAGATGTGATCCT[C/T]GTTCTGTAACTGGCA | 58513 |
rs559565612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364020 | TGCATCCTTAGCTGA[C/T]CTCTGGCCACCAGCT | 58513 |
rs559576468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396412 | GACTATAGGCGCGCA[C/T]CACCAAGCCTGGCTA | 58513 |
rs559578250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375947 | GACCGAGGGTCACTC[A/G]TAACTAGTGAGCTGG | 58513 |
rs559602010 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357551 | GGGAAGCAGGAGAGA[C/G]GAGGGCCAGATGGCA | 58513 |
rs559611018 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388873 | TTCTCATTAAGGACA[A/G]TGGAGGCTGGAAGGC | 58513 |
rs559645584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395196 | AGAGAGCGAGAGTTC[A/G]TCTCCAAAAAAAAAA | 58513 |
rs559663290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376878 | CAAGGCTTTGTGCAC[G/T]CCAATACAGAGCCAG | 58513 |
rs559682947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380521 | CTCACACACACGCAG[C/T]CATCTAAGGCTCTAG | 58513 |
rs559685792 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421099 | CCAGAGGCCCTTCCT[A/C]CTGAAAGACAGTGAA | 58513 |
rs559698166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389866 | CATGATATTTCCTAA[A/G]GCAACCTCTAAACAA | 58513 |
rs559800173 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422180 | GGTCACCCGCTGCAC[A/G]TGCGACCCCTCTCGC | 58513 |
rs559801619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452443 | AGGAGTGAAATTCCA[C/T]CTCGAAAAAAAAAAA | 58513 |
rs559805811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458896 | CAGGGATGCGTCCTG[A/G]GAGTTGCATCGTCAG | 58513 |
rs559816680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405958 | GGGCCATCAGGACGC[A/G]GGAACTGCAGGGGCC | 58513 |
rs559832589 | in-del | -/GTG | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419509 | AGGGAAGGGACCCTT[-/GTG]GAGTAAGGACAAGGC | 58513 |
rs559890072 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419462 | TCTCTGTCTCAAAAA[A/G/T]AAAAAATAAAAAAAT | 58513 |
rs559899067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367451 | ACACAGGACTGACTT[C/T]AGCAAAAACAATATG | 58513 |
rs559915971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452923 | TGCCTCAGCCTCCCG[A/G]ATAGCTAGGACTACA | 58513 |
rs559979633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470557 | ACTTAGCTATTAACA[C/T]CTATTATCGGTAGGA | 58513 |
rs559985307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432758 | CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCACA | 58513 |
rs559997740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433231 | CTCCTGGGTTCAAAC[A/G]ATTCTCCTGTCTCAG | 58513 |
rs559999026 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394056 | CACAGGATGCGGGCC[A/G]GGCCCTTGGACACAG | 58513 |
rs560004293 | in-del | -/AAAC | 0.0281438 | 0.115238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449251 | GATTTCTTAAAAAAC[-/AAAC]AAACAAACAAACAAA | 58513 |
rs560004536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385373 | CTCTCAGCAAGGCCC[C/T]CCTGCCCACTCTGGC | 58513 |
rs560041393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464804 | TTAAAAAATTCACGG[C/G]TGGGCATGGTGGCTC | 58513 |
rs560042132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380056 | CAGCTAAAGCTCCAG[C/T]GTCTAGTCACACAGA | 58513 |
rs560054016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462162 | TCTCCCTCTCAGTTT[C/T]CTCATCTAGAAACAA | 58513 |
rs560098068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375360 | CATGTGCATGCAAGA[C/G]CATACACGTGTACGT | 58513 |
rs560105120 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427610 | AAATGAAAGAAGGAA[A/G]GCTGGGTGTGGTGTC | 58513 |
rs560122215 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419025 | ATGGCCACAATGCAC[A/C]GGACAGTCCCCCACA | 58513 |
rs560151370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455713 | GCCTCTCTGTGCCTC[A/C]GCTTCTGCATCTGGA | 58513 |
rs560175402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467627 | TTACTCTAAAACTTC[A/G]TTCTCATCAATTTAG | 58513 |
rs560202233 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418487 | CGTGGAAATGGGTGC[G/T]GAGACCAAGCATTGT | 58513 |
rs560236382 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442269 | AACACAACCCCTTGG[A/G]GAAAAAAAGGGTTGC | 58513 |
rs560244295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392862 | AGTTCAAGACCAGCA[A/T]GGGCAACACAGAGAA | 58513 |
rs560275639 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436335 | GACCATGCTCACTTC[A/C]TTTAGAAGGAATTCT | 58513 |
rs560317066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450230 | CCAGCCTGGGCAACA[C/G]AGCTGTCTCTTAAAA | 58513 |
rs560336795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454137 | GTTCGCTGTTTTCCC[C/T]CCTTGAGGGCACAGA | 58513 |
rs560360450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398489 | GATAAAGATGGAGAA[A/G]TCCTACTCTAAAGAA | 58513 |
rs560389121 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402862 | AGTGCTGGGATGACA[C/G]GTGTAAGGCACTGCA | 58513 |
rs560441494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448306 | GAGGCCGAGGCAGGA[A/G]GATCACCAGAGTTTG | 58513 |
rs560441514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424384 | GAGGGTCTTGAGAGA[A/G]CCACCAGAAGATCAC | 58513 |
rs560442062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460045 | CTTTGGAGATTAAGG[C/T]AGGAGGATCCCTTAA | 58513 |
rs560447001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468108 | ACAAAAGGGACCCAC[A/G]GAAGGTACAAGGGAG | 58513 |
rs560451644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365725 | GGGAAAGCCCCCCCT[C/T]CCCCAGGGTCCCTCA | 58513 |
rs560469178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424862 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGATG | 58513 |
rs560515841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366310 | CAAGAGCGACTGCCA[C/T]GGTACAGAAGGTTCA | 58513 |
rs560527775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356459 | TGGGATTACAGGCAT[A/G]CGCTACCATGCCCAG | 58513 |
rs560530296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441692 | AGTACTCGGGTTTCT[C/T]ATCTGCTACCAAAGT | 58513 |
rs560567943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense, stop-gained | EPS15L1 | GRCh38.p7 | 19:16356988 | AACACTGGAGTAACA[C/T]CAAAGATAACATGCG | 58513 |
rs560572672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398025 | TTAAAAAGCCGGGGC[A/G]TCCACAAAAATAGGG | 58513 |
rs560637971 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378662 | CAGATACTAAGCGCC[A/G]CCACCTGGGGGGATG | 58513 |
rs560649137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399512 | TTCTGTGACATTCCC[A/G]CCCTTTAGAGGAGTG | 58513 |
rs560695677 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418905 | CCACCCCCCAGAGCC[A/G]TGAGAAATGTCTGTT | 58513 |
rs560699527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363284 | TAACTCTGGAAGTTT[C/T]GAAGCTAATGTTTAG | 58513 |
rs560704278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372557 | AGATTTCCACTAAAC[C/T]GTGACCTCACAGGGA | 58513 |
rs560716511 | in-del | -/ATGT | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375304 | CAGGTGCATGCATGC[-/ATGT]GTCTGCAGGCGTGGA | 58513 |
rs560717993 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399594 | TTTAGAGCTTCTGCC[A/C]ATTCCTGTGGTGTAA | 58513 |
rs560728045 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448553 | AAAAAAAAAGGGGGG[-/C]GGGAGAAAGGCCGGG | 58513 |
rs560729407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410164 | TGCAATTTAAAAATC[A/G]GCAAGAAAAAAATTT | 58513 |
rs560776406 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422970 | CTCGGGGAAAAAAAA[A/G]GGGGGGGGGGATTTC | 58513 |
rs560790761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410743 | CAGTGAGACCTTGTC[A/G]CTGCAAAAAAAAATT | 58513 |
rs560792672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404215 | CATCCCCCCAGAGGC[A/T]GAACGTCATAGAGTT | 58513 |
rs560806540 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451133 | TTTTTATACTTTTAG[C/T]AGAGACCGGGTCTCA | 58513 |
rs560829867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402155 | CCACCTGTGCCAGGC[C/T]GCAAGGCCTGGTGTG | 58513 |
rs560873977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445193 | CCAAGAGAAACAAGG[C/T]CTGGACTAATCCAGA | 58513 |
rs560875917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452307 | AAAAATTAGCCAAGC[A/G]TGGTGGCAGGCACCT | 58513 |
rs560877881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, missense | EPS15L1 | GRCh38.p7 | 19:16373917 | GGTCTGTACCTACCA[C/T]CCAGCAGCGAGTACA | 58513 |
rs560984903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425674 | CCTGTACTTCAAGAC[A/G]TTCAGGAGTAGTCCC | 58513 |
rs560991018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432513 | GCGGAGCTTGCAGTG[A/G]GCAGAGATTGCGCCA | 58513 |
rs560999064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426197 | GACATCACGTTCCCC[A/C]AGGTGGGAGGCCCAT | 58513 |
rs561015236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414690 | AGGCGTGAGCCAACA[C/T]GCCTGGCCTTTTTTT | 58513 |
rs561068871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370313 | GGGCCATGTTCACCC[C/T]GCCAGAAAAGCAGGG | 58513 |
rs561081583 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390452 | GACACTGGTAGGACT[A/G]AAAAACAAACAAACA | 58513 |
rs561139936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369810 | ATTCTGGCTTCTTTG[A/C]AAATTCGCATTTGTT | 58513 |
rs561164368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414249 | GAAAAAGAGACCTCG[A/G]ACCCCCAGCCGCAGG | 58513 |
rs561189455 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401374 | GGTGTTTAGAGAGCA[C/G/T]GAGCGCTCACTCTTA | 58513 |
rs561212215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463658 | CAAGGATGAATAAAA[C/T]AGGCACAGTCTCTGC | 58513 |
rs561214588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387958 | AGGGTCTCATATCCA[C/T]GTAACTGGAATCCCA | 58513 |
rs561228808 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444728 | CATTTCCAGACAAGT[-/T]TTTTTTTTTTTTTTT | 58513 |
rs561229039 | in-del | -/TACAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432615 | AAATACAAATACAAA[-/TACAAA]AATTAGCCGGCTGTT | 58513 |
rs561240272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469341 | GGCTCCAGTGTTGCG[A/G]AGTTCGAGGAGGATC | 58513 |
rs561246052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400854 | ACTGCCACTTCACTG[C/T]CAACTTTTATCCAAG | 58513 |
rs561248380 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360017 | GTTAACAATTGTTCT[A/G]GAACTACCAGAAATG | 58513 |
rs561254017 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443442 | GGCCGGGCGCAGTGG[C/T]TCACGCCTATAATCC | 58513 |
rs561313810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443755 | CGGATTATGGTCAGC[A/G]TCTCTGGGGGACGCC | 58513 |
rs561325620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437133 | GTTAAACACAGAATC[A/G]CCACATGACCCAGCA | 58513 |
rs561388178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423042 | AGGATTGAGGAGAAG[A/G]GACTCATGGTCAAGA | 58513 |
rs561395185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381822 | ATGTCCCTGGGCCTA[A/G]GGCCCGTGCGAGTCC | 58513 |
rs561397188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375909 | CCTATGTTCACCTCT[A/G]CTGACAGGTGGCCGA | 58513 |
rs561402296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423759 | TGCCTTTTAAGTCAC[A/G]GAGCTACAGCAAGCT | 58513 |
rs561422080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393565 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 58513 |
rs561434101 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471448 | AGCAGCTTCCAAGGA[C/G]GCAGGGGATCAGTCT | 58513 |
rs561446781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420506 | TGGGTGATGACTCTG[C/T]GACAGCTAGTTCTCA | 58513 |
rs561457611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450820 | GTCTCGCAAGGTGGT[C/G]ATTTGGGTCCCCAGA | 58513 |
rs561465591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417705 | ACAGGAGGCACCAGC[A/G]GTTCTCGGGCCCAGG | 58513 |
rs561470910 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459475 | ATGGGTGAGATTAAA[G/T]TGTTGAGGGAGGCAG | 58513 |
rs561482530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464070 | AGCGCCTGATCCAGC[A/C]TGGCTGGTGTGCCCA | 58513 |
rs561483563 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354803 | AGGATCACTTGAGCC[C/T]GGGGAAGTGGAGGTT | 58513 |
rs561483634 | snp | G/T | 0.000246718 | 0.011104 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361820 | CAGAGGCCTTAGAAG[G/T]TTTAGCTGCAGAGGA | 58513 |
rs561489041 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456144 | GGCAGAGGTTGCAGC[A/G]AGCCGAGGTTGTGCC | 58513 |
rs561499643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384331 | ACAACTCACAAGGAA[A/G]CACAATGGTGCCGCA | 58513 |
rs561506145 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397142 | TCATCCAGGCTGGAG[G/T]GCAGTGGCGTGATCT | 58513 |
rs561510274 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404062 | CTAACCCAGGCCCGA[C/G]ACCTGGCTTCCTTAC | 58513 |
rs561515006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398208 | ATCAGCATGAGTGCC[A/G]CTTCCTCGGCCCCCA | 58513 |
rs561519798 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355562 | TCCAGGTCTTGCAGC[C/T]GAGTCTGCTCACCCT | 58513 |
rs561524017 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366158 | CAGGACACGGTGTAG[-/C]CCCCTGGGACGGGCA | 58513 |
rs561623611 | snp | A/C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430624 | ATTTGACTTCTTTGA[A/C/T]GGTATCTAATTATCC | 58513 |
rs561630502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466129 | GAGGAGCTGGGACTA[C/T]AGGCATGTGCCACCA | 58513 |
rs561646008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397688 | CACAATGCTTTGCAT[A/T]TTTTTTTTAAAGTGT | 58513 |
rs561659784 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427870 | CTGCACTCCAGCCTG[G/T]GTGACAGAGCAAGAC | 58513 |
rs561712676 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377895 | ACCTCTGGCCCGGAC[A/C]CTCGGTCAGCCTCCA | 58513 |
rs561734468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384774 | TTTCCCTGGACGCCT[C/T]GCACCTGCAGGCCTG | 58513 |
rs561744669 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370921 | TAGGCTCCTTGGGAC[C/T]CCCTCCCCATCCTGG | 58513 |
rs561762997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429694 | CTCAGCCTGGCAGAT[A/G]GGGCCCTGTCACCTG | 58513 |
rs561775695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417353 | TGCTACGGGCTCTGG[A/C]TGAGGCTGATTCAAA | 58513 |
rs561799581 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435143 | TTTTTGTAGAGATGG[G/T]GTTTCAACATGATGG | 58513 |
rs561799932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460143 | AAAATTAGCTGGGCG[C/T]GGTGGTGTGCTGAGG | 58513 |
rs561814600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379394 | GTGGAGGGAGGGGCC[A/G]GGGGTCTTTAACTTT | 58513 |
rs561853282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448033 | AAAGGGCACTGGAGC[A/G]ATCGGCATCCATAGG | 58513 |
rs561865387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441486 | AAAAAAAAATTAGCC[A/G]GGTGTGGTAGCATGT | 58513 |
rs561868966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403603 | GCCTCCAGGCCAGCA[C/T]CACAGCCTCCCAAAA | 58513 |
rs561870191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391573 | CGGAAGAAGGCTATG[A/G]AGCACGCTCACTCCA | 58513 |
rs561911962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471502 | TCCGGGCTCCGGCGG[A/G]ACCCTGCCCGCCCGG | 58513 |
rs561942505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372236 | CTCCCTCGAGGAACC[G/T]CTGCAGGTTCCCAGG | 58513 |
rs561967047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414248 | GGAAAAAGAGACCTC[A/G]GACCCCCAGCCGCAG | 58513 |
rs562025203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452991 | TTTCTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 58513 |
rs562027945 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460066 | GATCCCTTAAGGTCA[A/G]GAATTCAAGACCAGC | 58513 |
rs562032328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409512 | ACCAACATTAACAAC[C/T]TGTGCTTCAAAAGAC | 58513 |
rs562047931 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451819 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCTACAAT | 58513 |
rs562083545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364744 | TCCTGTGAGCCCCAG[C/G]CTGTCCACTGGAGCA | 58513 |
rs562090228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377479 | ATGAGCTGCCCAACA[C/T]AGGGTGGCAGAGAGC | 58513 |
rs562126920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368354 | CATGCACAAGCATCA[C/T]TGATCCTACACAACA | 58513 |
rs562127045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375731 | GTTCACAGAAAATCT[C/G]CTCTAAATCCACACA | 58513 |
rs562179046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361501 | TCAGAAATAATACAA[C/T]GAATCTACCGTGAAG | 58513 |
rs562182235 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454226 | GAGTCTCCATGGGAC[A/G]GAATAAATACCTTAC | 58513 |
rs562246340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427153 | GACACTGGGAAATTT[G/T]ACTGAAGAGTTTTCA | 58513 |
rs562248342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424061 | GAGCTGGCTCTCCCA[C/G]TGACAGCTGGGCTTT | 58513 |
rs562252712 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445781 | GCCCGAGGCAACAGC[A/T]GAGAGGGGACGCACC | 58513 |
rs562263297 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400941 | ACGAAGACTGAGCAG[C/G]ACAAGCCAAAAGCGG | 58513 |
rs562304579 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450381 | TTCCTCTCCAGGGCA[G/T]GGAACGCATGCCTTA | 58513 |
rs562305897 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468359 | CATCAAAGCTGACTT[A/T]TTTTGAGACTGAGTC | 58513 |
rs562312816 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427789 | ATTCCAGCTACTTGG[A/G]AGACTGAGGCATGGG | 58513 |
rs562365122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361061 | CTCCTTGAAGCGACG[A/G]CATGTTACAATCTGG | 58513 |
rs562375213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406029 | GAGTGAGGTGGTGGT[C/T]GTGAGAATGGAGAGG | 58513 |
rs562414787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400009 | TCAATATTCTCATAA[C/T]CAGATGATAGACAAG | 58513 |
rs562418062 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442466 | TCTAGGGCAAACAAT[A/G]TAGTCACTCAGGAAA | 58513 |
rs562444178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458907 | CCTGAGAGTTGCATC[A/G]TCAGGTTAATTTCAT | 58513 |
rs562460865 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414712 | CTTTTTTTGGTTTTG[-/T]TTTTTTTTTTTTTTT | 58513 |
rs562482733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463218 | CTCAACTGACACAGC[C/T]ACAGCCCACCAGGCT | 58513 |
rs562499663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464885 | TCAGATCGAGACCAT[C/G]CTGCCTAACCAGTGA | 58513 |
rs562535201 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413577 | GTGGCTACAACATAG[C/G]GTTTTTATACAAGAA | 58513 |
rs562545585 | in-del | -/AAG | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466559 | AAAGTGTCCAGCAAA[-/AAG]AAGATGCCAAATAAA | 58513 |
rs562612676 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439062 | AGGGATCACTTAGCT[G/T]GTTTTTTTTCTGTTT | 58513 |
rs562647609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467768 | CCAGACACACTGGCC[A/G]GGTGCTGCTCTGGGA | 58513 |
rs562656875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424441 | GACCTGTGCCTACCA[A/G]TGAGTTTGGCCCCAC | 58513 |
rs562657194 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382255 | AGCTCCAGAATGCCC[A/G]CGTCATTTCCGAATC | 58513 |
rs562658274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412935 | CAAGTCCCTGGAGGA[A/G]AGCTATCTCTTCTCC | 58513 |
rs562659139 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413056 | CCCGCGCCGGCCAGT[A/G]CACCAGGTTCAAGGC | 58513 |
rs562714139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424977 | CAAGCATTTTTTAAA[C/G]ACATTTCATCACAAG | 58513 |
rs562726584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419149 | GAGGTGAGAGGCTCC[A/G]CGACACTCACAATCA | 58513 |
rs562763050 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356155 | AGGATGGGCCCTTGA[C/T]GCTGGTGGCCAAGAG | 58513 |
rs562765934 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448970 | GCATAAAAAAGAAAA[C/G]AATCAAATTAGAACA | 58513 |
rs562786814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419636 | ATTACAACAGAAGTT[C/T]CCCCTTTTACCAAAA | 58513 |
rs562829820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399572 | TTCTCTCAGAAAAAA[A/G]CCCTGGTTTAGAGCT | 58513 |
rs562846679 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438933 | AACATCCCCTGCCCA[C/T]CCCCAGTGGCCTGAC | 58513 |
rs562879910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442421 | CTGATTTAGAAAAAG[C/T]AAGCTTAATGTTCTT | 58513 |
rs562891237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454870 | CATGGTGGCTCACAC[C/T]TGTAACCCCAGCACT | 58513 |
rs562917334 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444851 | CCTACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 58513 |
rs562931530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393751 | CAGGGTGGGGTGCGG[A/G]CAGTGACTGGACCTG | 58513 |
rs562943632 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440551 | AACCCTCCAAGCTAT[C/T]TGTGCAACTTCCACG | 58513 |
rs562962384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366427 | ATTGGTTTTTGGGAG[A/G]AGCGGTTAAGAATTC | 58513 |
rs563006459 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393505 | ATACAAAAAATTAGC[C/T]GGGCGTGGTAGCGGG | 58513 |
rs563011283 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371313 | GAGGTCAAGAACTCA[C/T]GGCCACCCTGGGTGG | 58513 |
rs563018829 | snp | A/G | 1.68781e-05 | 0.00290495 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434503 | CACCTAGTTGGAAAG[A/G]AATAGCCCGAGTAAG | 58513 |
rs563019896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452922 | CTGCCTCAGCCTCCC[A/G]AATAGCTAGGACTAC | 58513 |
rs563032462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404868 | CCACCCACTGTGACC[A/G]TGCTCAGGGCCAGCA | 58513 |
rs563055732 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374038 | GACTTAAAATGCTGC[A/G]CGTGCATTGGCTGTT | 58513 |
rs563093120 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396106 | AGACCCTGTATCTTT[-/A]AAAAAAAAAAATTAA | 58513 |
rs563110236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455527 | TGCTGAGCCCTAAAC[A/G]TCTTCAGGAGAGACT | 58513 |
rs563155301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367235 | CTAGATATTTGCAGC[A/G]GGAACTACCGGGGAC | 58513 |
rs563200158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405450 | CCCCGTGGGATGGAT[C/T]CAGATGGTCAGCCCG | 58513 |
rs563208548 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468431 | GCTCACTGCAACCTC[C/T]GCCGCCTGGTTTCAA | 58513 |
rs563275932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439462 | TTAGGGAGGCCAAGA[G/T]GGGAGGATTGCTTGA | 58513 |
rs563324176 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367599 | TCTTCTCGAGGCTGC[A/G]CACGCCCCTAGCACC | 58513 |
rs563365722 | snp | A/G | 0.0019992 | 0.0315532 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427899 | ACTCCGTGTCAAAAA[A/G]AAAGAAAGAAAGAAA | 58513 |
rs563388041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471618 | CAGCCCAGCGCCTCC[A/G]CGGGTCCCCGGCCTG | 58513 |
rs563399698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414311 | TAGAAACAGATTCTT[C/T]CCCTAGAGCCTCCAA | 58513 |
rs563399734 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418363 | GGGCTGAGGAGCCGA[-/C]CCCCTGGGAAAACCT | 58513 |
rs563429423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408553 | CATTCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 58513 |
rs563454130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402731 | AAACCAAGACCCATC[C/T]CTGCAAAAAATACAA | 58513 |
rs563457454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452390 | GGCAGAGTTTGCAGC[A/G]AGCTGAGATTATGCT | 58513 |
rs563470476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446590 | CTGAGTTTGCCCTAC[C/T]CAGGACCACAACAGC | 58513 |
rs563497068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393862 | GGCTGCCATCCCCGG[C/T]GTATGTGGACACAAG | 58513 |
rs563499020 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401238 | GAGACAGATGAGCTC[A/G]CCAGCAGTGCCTTCC | 58513 |
rs563521816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376950 | GGAGGCACACACCAC[A/G]CACATACGGCACTTG | 58513 |
rs563522369 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363350 | CCTTGGATCTCTGGC[A/T]GCACCTCCAGAGAGC | 58513 |
rs563539425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382190 | CTCGCGAGGCGACAG[C/G]CTTTCAATAAACGCC | 58513 |
rs563610929 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457930 | CTCCGCAGCAGGAAC[A/C/T]CCCACCGCCTCCCAC | 58513 |
rs563640119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464192 | TGCAGATGGAAATCC[A/G]AGACAAATGTCTGTG | 58513 |
rs563650174 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416693 | GCGTCCTAGCTACTC[A/G]GGAGGCTGAGGTGGG | 58513 |
rs563671059 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381864 | GGATGGGGAGCCAAG[A/C/G]AGGTCTAGATGGGAA | 58513 |
rs563683660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426326 | TCCATAACTGCTGGC[C/T]TGTGCTCTTCAAAAT | 58513 |
rs563684392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376369 | GGCCAACTGGCCGCC[A/G]GCCTAACTCTGTCAT | 58513 |
rs563751950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464679 | CCAGGGGTGTCCAAT[C/T]TTTTGGCTTCCCTGG | 58513 |
rs563795197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418341 | AAGAACCCCAAGCCC[C/G]TGACCTGGGCTGAGG | 58513 |
rs563822413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376723 | GACAGGGAGAAGGAC[C/G]GAAGAGAAGGGGCCA | 58513 |
rs563824027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387468 | AAAAATTAGATGGGC[A/G]TGGTGGTGGATGCCT | 58513 |
rs563846838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458341 | TGGAGCATCATAGTC[A/G]GGGCATCAAAGCCAG | 58513 |
rs563858487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412098 | TTCATCAATTTGGAT[A/T]ATTTTTTATTTTTTT | 58513 |
rs563872018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444962 | GACCTCAGGTGATCC[A/G]CCTGCTTTGGCCTCC | 58513 |
rs563882236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438212 | ATAAAAATCAGCCAG[G/T]CGTGGTGGCAGGTGC | 58513 |
rs563892915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391703 | ATATGCAAAATACCC[A/G]GTGTCTGCCACGCCC | 58513 |
rs563902263 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355611 | CGGTCCTTGGAGTAC[A/G]GTGGCGACGGTGTGT | 58513 |
rs563905288 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417374 | CTGATTCAAATGGAA[A/G]ATGTCATTCTTCAAG | 58513 |
rs563913361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423888 | CCAAGAAGAAATTAC[A/G]TATGAAATTATAGCT | 58513 |
rs563927980 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374276 | GATAAGAACTGTTCA[A/C]GCACTTCCTAAGGGC | 58513 |
rs563981360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432601 | ATAAATACAAATACA[A/G]ATACAAATACAAATA | 58513 |
rs564032891 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392206 | CACTCGCAGGCACCA[C/T]GTACGCTCCACGAAG | 58513 |
rs564075644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467429 | TGCTAGGATTACAGG[C/T]GTCAGCCACTGCACC | 58513 |
rs564076871 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378300 | CCTGATTTTTCAGGC[C/T]CACCTCTGAAGTCAC | 58513 |
rs564090603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455085 | AGTGAGCCAGGATCA[C/T]ATCATTGCACTCCAG | 58513 |
rs564114327 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431158 | ACAGGAGAATTGCTC[A/G]AACCAGGGAGGCGGA | 58513 |
rs564150100 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461467 | TCTCTACAAAAAATA[A/C]AAAAATTGGCAGGGT | 58513 |
rs564161836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365511 | GAGCCTCTAGAACTG[C/T]GGGACAATCCATGTC | 58513 |
rs564212364 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455653 | TGTGGATTTGAGTCC[A/T]GTCCTGCTGCTGGAA | 58513 |
rs564218748 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440356 | GGGAATCACTTGATC[C/T]TGGGAGGTGGAGGTT | 58513 |
rs564223934 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439072 | TAGCTTGTTTTTTTT[C/G]TGTTTTTTTTTTTTT | 58513 |
rs564226545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405540 | TGCAGAGGTATACAA[C/T]GTCTATGACAGCAAA | 58513 |
rs564267895 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435195 | GGCCTCAAGTGATCC[A/G]CCTGCCTCGGCCTCC | 58513 |
rs564277333 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473697 | GGCATAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 58513 |
rs564277814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454014 | GCTTCTGTGAAACAA[C/T]ACAAACTGGCATTCC | 58513 |
rs564280476 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435813 | CTCTCGACCACAGTA[A/C]ACCCCAATTACAGCA | 58513 |
rs564305611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465342 | ACTCAATTCTGCATG[A/G]GCCAGGAGCACTGAT | 58513 |
rs564408251 | in-del | -/TT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435127 | CGGCTAATTTTTGTA[-/TT]TTTTGTAGAGATGGT | 58513 |
rs564411533 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468877 | TTTAATTAGCTGGGT[A/G]TGATTGGTGCTGCGC | 58513 |
rs564425086 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424251 | GGAGCATGTGGACTG[C/T]AGGCCCCCAGAAATG | 58513 |
rs564462715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447682 | GGAGAATCACTTGAA[C/T]CTGGGAGGCGGAGGC | 58513 |
rs564481373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459908 | TTCAACAAATGTTGG[C/T]TACACTATGGTACAT | 58513 |
rs564487502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372453 | ACTCAGACCCAAACT[C/G]ACATTTGGTCCTGTA | 58513 |
rs564494250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383580 | ATGGAGGCCTTCTCC[A/G]TGTGCTGGAAGGAGG | 58513 |
rs564503379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410095 | GCTGAGATTGCACCC[C/T]TGTGCTCCAGCCTAG | 58513 |
rs564516258 | snp | G/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369613 | AGGTCACCACAAAAG[G/T]CTCCCATGACATTTA | 58513 |
rs564536254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378051 | GGTGGGCAGATGGAT[A/G]GAATGGTAGTTGGAT | 58513 |
rs564546317 | snp | C/T | 6.58946e-05 | 0.0057396 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403791 | GTTTCCAGCTGGACT[C/T]GCCCAGCCTGAATGC | 58513 |
rs564553125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362669 | CATGAGCCACCATGC[A/G]TGGCTAATTTTTGTA | 58513 |
rs564568993 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422337 | TCCACCTGCATTACC[A/G]CGGGCCTTCAATACA | 58513 |
rs564603889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441577 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCGCTG | 58513 |
rs564652952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421900 | CCCACTCCTCAGCCC[A/G]CAAAGGCTGCCCTAC | 58513 |
rs564675224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377556 | ACACGAGGCACACTG[A/G]GTCTTTCCTGACTCC | 58513 |
rs564741577 | snp | A/G | 0.000191333 | 0.00977904 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355674 | CTCTGGAACCCGCCC[A/G]TGCCCTGTCCCGCCT | 58513 |
rs564791089 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415962 | CAGTTTGGATAACAC[A/G]GCCCCCAGGAGCTGA | 58513 |
rs564791444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417140 | AAGCTGCCACAGGCT[C/G]TGCCCATGACCTGCC | 58513 |
rs564819440 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371456 | TAGGTAAAAGCTGTT[C/T]GTTAGTGCAACTGTG | 58513 |
rs564822568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409653 | TCTTCAAATTCAGCT[A/G]TAGGCCAGGCGCAGT | 58513 |
rs564842268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453502 | GCGGATCATGAGGTC[A/G]GGAGATCGAGACCAT | 58513 |
rs564867927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457786 | TCAGAGAACAGACCT[A/T]TTCAGTTCCATCTGT | 58513 |
rs564891061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451621 | GCAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 58513 |
rs564901451 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445123 | CTTTGAGGCATGCAG[A/G]GTTATTAAATATCTG | 58513 |
rs564932642 | snp | C/T | 2.17059e-05 | 0.00329431 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437094 | CGTTTCAAAGTGCTT[C/T]CAAAAAAGGGAAGAC | 58513 |
rs564938126 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387775 | TGTCTCAAACAAACA[A/G]AAAAAAACCCCACTT | 58513 |
rs564944781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431428 | CCTGCCTCAGCTTCC[A/C]GAGTCGCTGGGACTA | 58513 |
rs564945542 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356404 | GCAACATTCACCTCC[C/G]AGGTTCAAGGGATTC | 58513 |
rs564993793 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414082 | AAAGCAGCGCGCTTT[A/C]TCCACCTGGTTGCCC | 58513 |
rs565008270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431971 | ACAGTAGTCGTGGGA[A/C]GTGAAACCCGAATAT | 58513 |
rs565021974 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446367 | AAACTCTCACTCTCA[-/CT]CTCTGCTAGCAAAGT | 58513 |
rs565051806 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356381 | CAATGGCGCGATCTC[A/G]GCTCATTGCAACATT | 58513 |
rs565063626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451016 | ATGGCAGTGGTGCAA[C/T]CTTGGCTCACTACAA | 58513 |
rs565077151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425606 | GCCACCAGCTCCAGG[A/G]CTGGCACCTTCCCAG | 58513 |
rs565136849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413670 | GCTCATGTTTCCATC[C/T]AGGGCAGACCCCTGC | 58513 |
rs565137681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419668 | AGAGCTGGGACCGTT[C/G]TAACAGACTTATTTA | 58513 |
rs565201641 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406725 | CTCAAACCAAAGATG[C/G]CAAAATGTGTACATC | 58513 |
rs565201695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414233 | GGCTGACCTCAGAAA[A/G]GAAAAAGAGACCTCG | 58513 |
rs565207010 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425030 | GTTAAGAACTCCCGA[A/G]AAACATCCTACTGTG | 58513 |
rs565216926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468399 | TGCCCAGGCTGGGGT[A/G]CAGTGGCGCGATCTC | 58513 |
rs565218000 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358471 | GCCGATGCAAAACCA[A/G]TAGTGGCTGGGAAAC | 58513 |
rs565233223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393533 | GGGCGCCTGTAGTCC[C/T]AGCTACTTGGGAGGC | 58513 |
rs565259140 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368684 | ATCTCACAAAACCAT[C/T]ATTCACCCTACATAA | 58513 |
rs565270227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436603 | TCTATTCTGAATAAC[C/T]AACACAAGCAGCAAA | 58513 |
rs565292473 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407469 | CGCCACCACGCCCAG[C/T]TGCGTGATTTTTTTG | 58513 |
rs565311029 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458701 | ACTCACACACACTCA[C/G]CCACACACACATACA | 58513 |
rs565313261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427966 | CCCAGCACTTTGGGA[A/G]GCCAAGGCGGGTGGA | 58513 |
rs565357668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443089 | TACGTGCGTTGGTGT[C/T]TTAGTAAGTGAGGTG | 58513 |
rs565372041 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405533 | CAGCGTGTGCAGAGG[C/T]ATACAACGTCTATGA | 58513 |
rs565406258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387075 | AGGGACAACGTAAAA[C/T]GGTGATTATAACTGT | 58513 |
rs565407830 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362074 | GGTGGGCACAAGCCC[A/G]GGGCGCTTCTCTGAG | 58513 |
rs565425310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469305 | ACTGAAAGGAGAGAG[A/G]ATGAAGAGTGAAGAC | 58513 |
rs565485854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453096 | TGAGCCACCGCGCCC[A/G]GGCTTTATTTTATTT | 58513 |
rs565490656 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420740 | TGACTTCAGCCCTGG[-/C]CAGTGGCAAGAGGAG | 58513 |
rs565494733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450154 | CAGGAGGCTGAGGCA[A/G]AAGGATTACCTGAGC | 58513 |
rs565503500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360088 | TTTTTTATGCTTTTC[A/G]AAAAAACGAGCCCTT | 58513 |
rs565531559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433039 | TGGACTCAAACTCCT[A/G]GACTCAAGTAATCTG | 58513 |
rs565535370 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452731 | AAATATTGATAACTG[C/T]TGTAAATGGGCAGTG | 58513 |
rs565543529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433407 | AAAGTGCTGGGATTA[C/T]GGGCGTGAGCCACCG | 58513 |
rs565579430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421955 | GGACTCTGAAGACCA[A/C]CCTTCTATGTCCCTG | 58513 |
rs565589658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416191 | GGGATCCCCCAGCTA[A/G]GACCAGGATCCATCC | 58513 |
rs565625084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377065 | AGCAGGGAGGCCCTG[G/T]TCCCCCGCCATCCGG | 58513 |
rs565630574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383135 | GCAGCTGATGGAACG[C/T]TGGAATCAAAACAAG | 58513 |
rs565631292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377629 | TCAGAGACACGCCCC[A/C]CCCTCACCTGTATGC | 58513 |
rs565667868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371661 | CGCAACGCAGGGCCG[C/T]GCTGGCAGGAAGTGG | 58513 |
rs565773699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395697 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAA | 58513 |
rs565785013 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407506 | TGTTTTTGTATTTTT[A/T]GTATAGACTGGGTTT | 58513 |
rs565846783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471726 | CGCGAGGGTCGCTCG[A/G]GCACGGGAGGCCGCG | 58513 |
rs565857213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357139 | GAAAGAAGCACACAG[A/G]AACACTCACGGCCTC | 58513 |
rs565863395 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420255 | TTAGTGATTTCCTGT[A/G]TCATTTCCATGTCAT | 58513 |
rs565886775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381684 | CCCAGGCCTGTCCGA[G/T]ACATGAGGGGCAGTG | 58513 |
rs565898862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369981 | TGTTCCTCCCTACGG[A/G]GTGTGCCAATGTCGC | 58513 |
rs565983810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414006 | TACAGTCCCTTCCCC[A/G]TCAACTGTAGGTAGG | 58513 |
rs565994491 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382596 | CTAAAAATGGGCTGA[A/C/T]GACTAACCCAGTATT | 58513 |
rs565999820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362869 | GGCTCCAAGGGGCAG[C/T]GTTTATCTGGGCCTT | 58513 |
rs566032253 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451903 | AGCACTTTGGGAGGT[C/T]GAGGCAGGCAGTTAC | 58513 |
rs566037346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360034 | AACTACCAGAAATGC[C/T]AAGCCAAATGATACC | 58513 |
rs566042620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402284 | TCACACCAGGGGACC[A/G]GAGCCCCATACTGTA | 58513 |
rs566045486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407008 | GGTGCTGCCTATGAA[C/T]CAGGAAGTGGGTCCT | 58513 |
rs566073598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466199 | CAGCATGTTGGCCAG[A/G]CTGGTCTTGAACTCT | 58513 |
rs566081358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363074 | ACCAAGAAGCAGAGG[C/T]CTGTTAAGATCTGCT | 58513 |
rs566180856 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414877 | ACCAGGCCTGGCTAA[C/T]TTTTTATTTTTTGTA | 58513 |
rs566195401 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446528 | TCATCCTCCCGACAA[C/T]GCTAAAGGGCAGGTA | 58513 |
rs566218242 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356646 | AACACTGACAAAAGG[A/T]GTGGCACTTACACTG | 58513 |
rs566225245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464309 | AGAGCTAATGGTCTG[C/T]ACTCCATGCAGGAGC | 58513 |
rs566241573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425875 | GGCAGGCCACAGCCA[A/T]AGAAATAAATTCCTT | 58513 |
rs566254041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399815 | GTGTGAGCCATTGTG[C/T]CCGGCCAGTTCCTAT | 58513 |
rs566357897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442614 | GAAAAGAAGTTTCCA[C/G]GCATTATCATAAATC | 58513 |
rs566415181 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374425 | CAAATTGTGCAACAG[C/G]TCCCTAAAAAGCCTG | 58513 |
rs566422088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457991 | TCCAAAGTGTACCCC[A/G]GGCCTTCCCAACATT | 58513 |
rs566426247 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449275 | AAACAAACAAACAAA[A/C]AAAAAAACACGAAGA | 58513 |
rs566428810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366642 | TCAGAAGGAACATCA[A/G]CAACAACAACGGTTT | 58513 |
rs566444400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359092 | ACAAGTGAGGTGCGG[A/G]TGACCTGGGCCCCCC | 58513 |
rs566445321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404427 | GGCCAGGAAGTCAAG[C/T]CACAGGTGCTTGGAC | 58513 |
rs566466433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392636 | AGGGGCCTCAGGAAT[A/G]ACAGAAGTGTTCTCA | 58513 |
rs566470739 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428405 | AAAGAAAGAAAGAAA[A/C]GGGAGGGAGGGAAGG | 58513 |
rs566488579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449747 | AACTGGTAACACCCC[A/G]GATGTCCTCCAATAA | 58513 |
rs566506424 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458649 | TCCCTGGCCATCTCC[C/T]ACCTTGCCGGGCTGA | 58513 |
rs566530856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405699 | ACACTGCATTTGTGC[A/G]AACGGGAAGGGGAGG | 58513 |
rs566588204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417488 | GCCTCTGATATTTCC[A/G]ATAACAACCTGGGAG | 58513 |
rs566590431 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443231 | TGGGCAGGGAAAAGA[A/G]GACTATCTTGGGGGC | 58513 |
rs566622832 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384070 | CATGGGCTCCAGGAG[G/T]GGGGCTGTGTTCTGC | 58513 |
rs566622867 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473787 | AACATGATGAAATCC[C/T]GTGTCTACTAAAAAT | 58513 |
rs566683595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366021 | GTTTGCAGGAAACAG[A/C]AATGTTACTGTGCAT | 58513 |
rs566691203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364335 | CCACGCGGGCAGGAC[A/T]GGAATGTGGCCCCTC | 58513 |
rs566709335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417754 | GTACACAGGGTGAGG[C/T]AGCAAAAGTGTCAGC | 58513 |
rs566711730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424039 | AACACGGGGCAGCCT[G/T]GCCGTGGAGCTGGCT | 58513 |
rs566727195 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364827 | CACCTCCACCCTCCC[A/G]TCCCTAGAAGCCTCA | 58513 |
rs566727292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357746 | CCCTGGGAGGAAGGG[C/G]TGAGTCTTGACTTCT | 58513 |
rs566746126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460796 | TGTCTGGGACCCCCC[A/C]ACCACAAACAGTGCC | 58513 |
rs566758991 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454447 | TTCCTCATGGCTTCC[C/T]ATGTTCCCTGGTGTA | 58513 |
rs566782405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398396 | ACTGCAGCTGGAGAC[A/G]GTGCTGAGTGGACGT | 58513 |
rs566809924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448556 | AAAAAAAGGGGGGGG[A/G]AGAAAGGCCGGGCGC | 58513 |
rs566821993 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455116 | CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 58513 |
rs566840590 | in-del | -/AAAGAGGAAGGTAAGTTTACCT | 0.00119737 | 0.0244387 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473591 | AGTACTGGAAGAACA[-/AAAGAGGAAGGTAAGTTTACCT]AAAGATTCATAACTA | 58513 |
rs566843747 | in-del | -/AAAAGAAAAGAA | 0.0372196 | 0.131242 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428589 | AAAGGAAAAGAAAAG[-/AAAAGAAAAGAA]AAAAGAAAAGAAAAA | 58513 |
rs566864616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358393 | TGTCTTAGCCCTGGA[C/T]GGGGCCACCTTCTAG | 58513 |
rs566865148 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367587 | ATTTCTCAAGCTTCT[C/T]CTCGAGGCTGCGCAC | 58513 |
rs566924916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422802 | TCTCTACTAAAAACA[C/T]GAAAAATTAGCCAGG | 58513 |
rs566933141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391815 | CAGCCGGGCTGAGAC[A/G]CCTGCACTTACTCCT | 58513 |
rs566949870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469511 | AGACACACAAATCAC[A/T]GAGATGCTGTTGGGA | 58513 |
rs566962890 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369478 | GTGGGCAGGGGGCTG[C/T]TGAACCCAATGGCTG | 58513 |
rs567010166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470112 | CCTGGCCAGGCGCAG[C/T]GGCTAACGCCTGTAA | 58513 |
rs567022301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381711 | AGTGTCGGCCTGCAG[C/T]TTAGCTTTAAAATGG | 58513 |
rs567042469 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405531 | TACAGCGTGTGCAGA[A/G]GTATACAACGTCTAT | 58513 |
rs567059560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382015 | CGCGCAATAGGACCC[A/G]GGCAATAAAACCACA | 58513 |
rs567066615 | snp | A/T | 1.65493e-05 | 0.00287652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440767 | CATGCCTAGTAATAC[A/T]TGACAGTGGAGGAAT | 58513 |
rs567075616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397369 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 58513 |
rs567085224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443935 | CAGGTGTGGTGGTGT[A/G]CGCCTGTAATCCCAG | 58513 |
rs567095083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409776 | AACCCTGTCTCTACT[A/G]AAAACACAAAAATTA | 58513 |
rs567106222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361639 | TGGCAGTGTAGAATA[A/T]ATAACGCGAGGGACA | 58513 |
rs567111694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394803 | TAGGAAACTGAAGTA[C/T]TGAAGGGTTCAAGGG | 58513 |
rs567134039 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378368 | ACTGACCCCCCAGCC[A/G]CTGACTCAGCCTCCT | 58513 |
rs567134109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388229 | TGTATTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 58513 |
rs567140689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438442 | TATATTTTCCAAAAA[C/T]TATGAGCTCCCAACA | 58513 |
rs567143033 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355238 | CAGAGATTAAAGAAG[C/T]TTCTCTTGTTTTGTA | 58513 |
rs567148189 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401200 | AAGAGGGAGGCGGTG[C/T]ACCCAGCGGGGGCCA | 58513 |
rs567152377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432887 | AGCTTATTGCAGCCT[C/T]GACTTCCCAGGCTCA | 58513 |
rs567243793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432437 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 58513 |
rs567250186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388283 | GGCCTCAAGTGATCC[A/G]CCCACCTCAGCCTCC | 58513 |
rs567265352 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16355764 | CCAGGTCCTCCTGCT[C/G]CTGCCGCCGCAGCCG | 58513 |
rs567273973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426027 | GAACTCTCATGGAAG[A/G]GTCTGAGAGTCATGG | 58513 |
rs567295095 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356644 | AGAACACTGACAAAA[C/G]GTGTGGCACTTACAC | 58513 |
rs567336755 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426489 | AAATTCAAAAAAAAA[A/T]TTAGCTGGCTGTGGT | 58513 |
rs567354068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362121 | GCTAACAGGCTGGAC[A/G]GGGGTACCCTGGGGA | 58513 |
rs567357880 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453756 | GGGTACTATGTTCAC[C/T]ACCAGGGTGACAGGA | 58513 |
rs567358405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464425 | CCAGCCACTGGCCAC[C/T]CTCTCGGCAAGCAGA | 58513 |
rs567365198 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420918 | GGCCTCCTGCCCCCG[-/C]CCTCACCCTGCCAGG | 58513 |
rs567496747 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406804 | CAGGAGGACAAGAGG[A/G]AACTCACTGGCCACA | 58513 |
rs567510299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430296 | TGTGGGGGTGTCTAA[C/T]GGACAGGGCAGGTGA | 58513 |
rs567513084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400470 | GTTCCAGATGTACCA[C/T]TGTGGATACACTATT | 58513 |
rs567516323 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439584 | GTGGCCTCAGGTACA[C/T]GAGAGGCTGAGGCAG | 58513 |
rs567523627 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375050 | TGTGTGCAGGCATGC[A/C]CAATGCAGTATGTGA | 58513 |
rs567573526 | snp | A/T | 3.29533e-05 | 0.00405901 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394047 | GCTCTAGGGCACAGG[A/T]TGCGGGCCGGGCCCT | 58513 |
rs567578790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438030 | ACTGGACTCACCTTG[A/G]GGACATCGCTTAAAT | 58513 |
rs567582545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431554 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 58513 |
rs567586618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424721 | GCTGGAGTGCAGTGG[C/T]GCGCTCTCAGCTCAC | 58513 |
rs567600574 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455754 | AGCACTCCCACCCCC[-/G]GGGACTTGTCAATCA | 58513 |
rs567616010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462581 | GAGGCTGAGGCAGAA[C/T]TGCTTGAGCCCAGAT | 58513 |
rs567625629 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411481 | GGCGCCTACGGGAGA[A/G]ACAATCAGGTTCTAA | 58513 |
rs567668761 | snp | A/C | 0.00143343 | 0.0267331 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413768 | AAAACGAACGAGACC[A/C]TTACCTGCACCTCGC | 58513 |
rs567696883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422576 | TCTCCACGCAGCAAC[C/T]GTACAGAAAAGCCAC | 58513 |
rs567706529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413021 | TGAGGTTTTGAAGAT[A/T]ATGCCAGTGCAGAAA | 58513 |
rs567772877 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463671 | AACAGGCACAGTCTC[C/T]GCCCTTGTGGACCTA | 58513 |
rs567776371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406245 | GGAAGCTGGGGTCTC[C/T]GTTCCCCAGTCTCCC | 58513 |
rs567778534 | snp | A/G | 0.00993419 | 0.0697739 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354829 | AGGTTGCAGTGAGCT[A/G]AGATCACACCACTGC | 58513 |
rs567793378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368595 | CATTCCACACAACAG[A/G]TGGTGCCCACACAAC | 58513 |
rs567817263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401369 | AGTGTGGTGTTTAGA[A/G]AGCACGAGCGCTCAC | 58513 |
rs567840059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374015 | CACACAGATCTGCAG[G/T]TGCTCCGGACTTAAA | 58513 |
rs567862371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447855 | TCAAGACTGACTCTA[C/T]AGCTAGAGTAGTTAA | 58513 |
rs567899545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386311 | CCAGACCTTCCTGAC[A/G]TCGATGTACAACATC | 58513 |
rs567913733 | in-del | -/AAAAC | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425807 | AGACTCTGTCTCTAT[-/AAAAC]AAAACAAAACAAAAC | 58513 |
rs567923286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427999 | ACTAGGCAGGAGATC[A/G]AGACCATCCTGACCA | 58513 |
rs567923417 | in-del | -/GAAAA | 0.0182705 | 0.0938161 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428578 | AAAGGAAAAGGAAAG[-/GAAAA]GAAAAGAAAAGAAAA | 58513 |
rs567928693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459343 | TCCTGAAGTTGATTT[A/G]ATGGAAAAGCTGCTG | 58513 |
rs567950836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467926 | CTCACTTGTAAAAGG[A/G]GAATAAAAGCCTCCT | 58513 |
rs567961294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468514 | CTATGCCTGGCTAAC[G/T]TTTGTATTTTTAGTA | 58513 |
rs567980295 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428828 | AGTGAGACCACCTGC[A/C]GGAACTCAGACTCTC | 58513 |
rs567986813 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403218 | AACGGCTGCAGGCCA[C/G]GAGAAGCCAGCGCCC | 58513 |
rs567993460 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406636 | CTCCTTCCAGGCCAC[A/G]GCCCATGGATCCAGG | 58513 |
rs567995691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380316 | ACCTAAGGCTCTGGC[A/G]TCTAATCACACAGAC | 58513 |
rs568020716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409860 | GGAGAATCACTTGAA[C/T]CTGGGAGGCGGAGGT | 58513 |
rs568029185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378213 | GCAGGTAGGTAGGTA[A/G]GTAGGCACTTCCTAT | 58513 |
rs568029322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371963 | GGTCTGTGCTGCATC[C/T]GCCTGAAAGAAACCA | 58513 |
rs568085412 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452925 | CCTCAGCCTCCCGAA[C/T]AGCTAGGACTACAGG | 58513 |
rs568108017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364869 | GCCGCCCACCAGCTC[A/G]GCTCCCTTCCCTGTG | 58513 |
rs568165664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410248 | CAAATGGCTAATAAG[C/T]ACATGGAAAGATACT | 58513 |
rs568168176 | snp | A/C/T | 1.66032e-05 | 0.0028812 | synonymous-codon, missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403904 | GTCAGATTCCTGAGA[A/C/T]TGGATTTGCGTTTTC | 58513 |
rs568199459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402878 | GTGTAAGGCACTGCA[C/T]TGCGCAAAGCAACAT | 58513 |
rs568199464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395787 | TGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCTG | 58513 |
rs568235630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396499 | GAACTCCTGAGCTCA[A/G]CTGATCCTCCCACCT | 58513 |
rs568236773 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369917 | GAGAGATGCTATCTA[C/T]GCATGAGCCAGGCAC | 58513 |
rs568259012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383226 | AATAGGAAGTGAGAC[C/T]GGCTCTGAAATCACA | 58513 |
rs568259814 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389988 | ACATGGGATAAAAAG[C/G]AAGCAAATAATAAAA | 58513 |
rs568282848 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455692 | AACCCTGGGGCAGGA[A/C/T]GAGCAGCCTCTCTGT | 58513 |
rs568284656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376491 | ATGGGGAAGAGGGGC[A/G]GGGCCTGTAGGAAGT | 58513 |
rs568344605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363532 | CCATCCCAGGCCTCA[C/T]TTTTGAGGCCCCAGG | 58513 |
rs568347606 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459084 | AATGCTAAGTAGCTG[A/C/T]GTATCTAAACATATC | 58513 |
rs568350003 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472765 | AGTTGGAGACCAGCC[G/T]GGCCAGTATGGTGAA | 58513 |
rs568369653 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374191 | ATGACCTCCCTCCCC[A/G]CCTTTCCTCTTCCAG | 58513 |
rs568380325 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383700 | GCGCCGCCAGGGCAC[A/G]CACACACGCGTCTTT | 58513 |
rs568407144 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429992 | GACCCAGGTGTGACA[A/G]CCAAAAATGTCCCCA | 58513 |
rs568432828 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394306 | GAATTCACTCCTCTC[C/T]TCCCATGCTGGGTTT | 58513 |
rs568464004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439678 | CCTGGGCAACAGAGC[A/G]AGGCTCAAAAAATAA | 58513 |
rs568464456 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417344 | CCACACAGATGCTAC[A/G]GGCTCTGGCTGAGGC | 58513 |
rs568476160 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384021 | AGCTGCTCCAGGGGA[-/C]CCCCCCACACCGGCC | 58513 |
rs568491033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446762 | GGGAAAATGCACGTC[C/T]GTGATGACGTGCTGG | 58513 |
rs568497485 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440683 | CTAGCCATGAAAGAT[A/G]GCTCCAAGTGTTTAA | 58513 |
rs568523771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357596 | GGGCAAGGTGCAGGA[A/G]CAGATAAATGCAAGG | 58513 |
rs568524204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464812 | TTCACGGGTGGGCAT[A/G]GTGGCTCACGCCTGT | 58513 |
rs568544867 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363207 | GTCCCTGGGCATTCA[A/G]CGTGGTCCACGCAGC | 58513 |
rs568551768 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392866 | CAAGACCAGCATGGG[A/C]AACACAGAGAAAAAT | 58513 |
rs568559986 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389165 | AAAAAGAAAAGAAAA[C/G]AATAATAGCTGGGTG | 58513 |
rs568575387 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419601 | CGTTTCCCACCTCCC[A/G]TGTAGCTGCGGCAGA | 58513 |
rs568593673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400368 | AAACAAAAAAAAAAA[A/C]AAACCCCTGACTTTT | 58513 |
rs568593901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393232 | GGGTCTCCTTTTGGG[A/G]GGATGAGAATGTTGT | 58513 |
rs568604986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458072 | CTCCCTAACAGAGCA[C/T]ACTGCCCAGGACTCG | 58513 |
rs568635814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458569 | CCACTCCTCTGCTCA[C/G]AAAGGCTCTTCAGGG | 58513 |
rs568648549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420742 | ACTTCAGCCCTGGCC[A/G]GTGGCAAGAGGAGTG | 58513 |
rs568676648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408218 | CTCGAGGTTAGGAAG[A/G]GGAGCTCAGAGCAAA | 58513 |
rs568677533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461577 | CGGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 58513 |
rs568681418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414495 | ATCCTCCGCCTCCCC[A/G]GTTCAAGCGATTCTC | 58513 |
rs568707068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370769 | CCGTTCCTTGGCACC[A/G]TCAGCAGGTCCCACC | 58513 |
rs568713855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421138 | CACGGAGCGCGGGCT[G/T]CGAGCCTTGGCACGT | 58513 |
rs568723098 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374882 | GCATATGTGTGTGCA[A/C/T]GTTTGCATGCATGCA | 58513 |
rs568756264 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452068 | TGCTTAAACCCAGGA[A/G]GCGTAGGTTGCAGTG | 58513 |
rs568781417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363187 | CCCTCTATCTGCCCA[A/G]CGGAGTCCCTGGGCA | 58513 |
rs568806756 | in-del | -/AAAG | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427899 | CTCCGTGTCAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 58513 |
rs568818462 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354851 | CACCACTGCACTCCA[A/C]CCTGGGTGACAGAGC | 58513 |
rs568820247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360360 | TGTCACCATTTTGTA[C/T]AGACCCCCAGTGCGC | 58513 |
rs568893444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443830 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 58513 |
rs568896371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430947 | TGGATACAAAGATGT[A/C]TGCATGGCCGGGCAC | 58513 |
rs568924542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455181 | GGAGTGCAGTGGCAC[A/G]ACCATAGCTCACTGT | 58513 |
rs568924564 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461229 | GAATGGCATGAACCC[A/G]GGAGACGGAGCTTGC | 58513 |
rs568941371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466459 | TACACATTGGGCTCA[C/T]TTCTTTATATCTGGG | 58513 |
rs568968913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366875 | CTGTATTTTTCAAAC[C/T]TTCTAGGTCTAGTTC | 58513 |
rs569001708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411615 | GATTGGTATTAAAAT[G/T]TGCAGATGCTCAAGT | 58513 |
rs569005237 | in-del | -/A | 0.417521 | 0.185571 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452634 | GCAAAATGTCATCTG[-/A]AAAAAAAAAAAAAAA | 58513 |
rs569008680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379162 | TACAAAAAATTAGCC[A/G]GTCGTGGTGGCGGGC | 58513 |
rs569013854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405350 | CGCCAAGGAGACTGC[A/G]CTGGGCTCTGTGGTG | 58513 |
rs569041506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379656 | AGGCCTTCAGTGTCT[A/T]GTCACACAGACAAGG | 58513 |
rs569069482 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441269 | TGAGGTCAGGAGTGC[A/G]AGACCAGTCTGGCTA | 58513 |
rs569069597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448416 | ATGCCTGTAATCCCA[A/G]CTACTCGGGAGGCTG | 58513 |
rs569114049 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384598 | TGAGGGCCGGACACC[A/G]ACGGGTCCAGTCTGG | 58513 |
rs569118207 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395017 | CTGAGGTCAAGAGTT[C/T]GAGACCAGACTGGGC | 58513 |
rs569156766 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429569 | AGGCTCAGGCCTCAC[A/C]AGCCCACACAGCCAA | 58513 |
rs569157741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449349 | TACCAAAGAGGAAAT[A/G]TAGCAGATGGCAAAT | 58513 |
rs569166919 | in-del | -/ACAATGGA | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434026 | ATTCCCACATTCAGC[-/ACAATGGA]AAGGGGGAAAGCCCA | 58513 |
rs569180610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367626 | CACCCGGGATCGGGG[A/C]TGTGATGGGGCTGGC | 58513 |
rs569231590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436047 | ACCACAGTGATTGCC[A/G]CTGGCAAAGTGCTTG | 58513 |
rs569245222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430139 | ACTTCTACCAGAGTC[C/T]CCCTCACCCTGGAGG | 58513 |
rs569246288 | in-del | -/AAAT | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432567 | GCGAGACTCTGTCTC[-/AAAT]AAATAAATAAATAAA | 58513 |
rs569254902 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407573 | TCAAGTGATCCGCCA[G/T]ACTCAGTCTCCCAAA | 58513 |
rs569256775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460934 | TTCATCTTTCCCCTT[C/T]GGAGAGTGTGAAATG | 58513 |
rs569280808 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464454 | GACATCCTGTCAGTT[C/T]GGCCGATTTGTAGCC | 58513 |
rs569282639 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423523 | AGCAATGAGCCGTGA[C/T]TGCACCACTGCACTC | 58513 |
rs569305924 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458890 | TAACTACAGGGATGC[A/G]TCCTGAGAGTTGCAT | 58513 |
rs569328940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384953 | GTCAGGGCTCACCCC[A/G]CGGGACTGCAGTGCA | 58513 |
rs569344917 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424066 | GGCTCTCCCAGTGAC[A/G]GCTGGGCTTTAAGGC | 58513 |
rs569418356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365801 | AGCTCTGTGAAAAGC[A/G]GGCCCAGCATACCAC | 58513 |
rs569455198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358982 | GAGGGAAGAGGTTTC[C/T]CGGGAACAGCCACAC | 58513 |
rs569469038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438089 | CAGGTGTGGTGGCTC[A/T]TGTCTGTAATCCTAG | 58513 |
rs569473733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424783 | CTCCTGCCTCAGCCT[C/T]CCGAGTGGCTGGGAT | 58513 |
rs569486510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435545 | AATTTTTTAATTTTT[A/G]AAAGACAAAAACCAA | 58513 |
rs569501962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404268 | ATCTGTGAGGAGCCT[C/G]AGAGACACCTGAGGA | 58513 |
rs569534913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438732 | AGGTGGGATCTCACT[A/G]TGTTGCCCAGGCTGG | 58513 |
rs569537982 | snp | C/G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359846 | CTAGCCTGGGCAACA[C/G/T]AGCGAGACTCATCTC | 58513 |
rs569553094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398126 | GCAGCCAACTTAGGG[A/G]TGCAGGACAGTTATG | 58513 |
rs569555985 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460706 | GGGTGCCGCGGGCAC[A/G]GAGCGTTCTAGTTCT | 58513 |
rs569562614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427195 | TGTCGGAGGCCAAGG[C/G]GGGAGGTCGCTTGAG | 58513 |
rs569588432 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382089 | AAATCAGAGCCGCCT[A/G]ACCCTCCAGGCTGAC | 58513 |
rs569624606 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389083 | ACATGGTGAAACTCC[A/G]TCTGCATTAAAAATA | 58513 |
rs569685643 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376955 | CACACACCACGCACA[C/T]ACGGCACTTGCGTGG | 58513 |
rs569722623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376561 | TGGGGCAGAGGGGAG[A/C]CCCGAGCCATCCTGC | 58513 |
rs569735897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362964 | GAGGTGAGAGAGAAG[A/T]GTTCAGAAATGGAGG | 58513 |
rs569737377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421151 | CTTCGAGCCTTGGCA[C/T]GTGCACCTTGCTCAG | 58513 |
rs569774967 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356574 | CTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 58513 |
rs569886727 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461578 | GGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 58513 |
rs569909651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394233 | GTTTAAGATGAGAAG[A/G]AAGGTACTGCTGGCT | 58513 |
rs569935057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413149 | CGGCCACTGCCATCC[A/G]CAGGGCCATCATACT | 58513 |
rs569940450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470154 | TGGGAGGCCAAGGCG[A/G]GTGGATCACTCGAGT | 58513 |
rs569942898 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411967 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 58513 |
rs569965270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432923 | GATTCTCCCACCTCA[A/G]CCTCTAGAGTAGCTG | 58513 |
rs569983179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388406 | GAGCAAAGCCTAAAC[A/G]GTATAAACACCAAGA | 58513 |
rs569988391 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391312 | GAAAGGTCAATGAAA[G/T]TGGTAAACAGATCAC | 58513 |
rs570001920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457479 | GCACCAAAGCAGTGC[C/T]AGAGACAGGCTTGCC | 58513 |
rs570014547 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388526 | ACAGGATAACAATGA[C/G]CTGAAGAAATACTCC | 58513 |
rs570039645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375970 | TGAGCTGGGGGCATG[C/T]GGAGCCTGCTAGGTC | 58513 |
rs570071256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407387 | CTCAGCTCACTGCAA[A/C]CTCTGCCTCCTGGGT | 58513 |
rs570087311 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424043 | CGGGGCAGCCTTGCC[A/G]TGGAGCTGGCTCTCC | 58513 |
rs570089670 | snp | C/T | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406909 | GTGATTAGGTACAGC[C/T]CTTGTGAGTGGGATT | 58513 |
rs570096577 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451804 | AGAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 58513 |
rs570099356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417460 | AACCTGTGATGAGCA[A/G]ACTTCCAGGTGAGCC | 58513 |
rs570179048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362185 | TAACGGGTTGTGAAC[A/G]ACACAGGAAAAACAC | 58513 |
rs570190901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386406 | AGATCAACCCTCCTG[A/C]AGATAGCACCTATCA | 58513 |
rs570230187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431594 | TGCGTGAGCCACCGT[A/G]CCGGGCCAGAAGGAA | 58513 |
rs570243645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441819 | GAAGGAGGCCTGCAC[A/C]GGCTGGCCCTGACCT | 58513 |
rs570258865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457015 | ATATGAGATGGTAAA[C/T]GGCAGAAATCCGCTG | 58513 |
rs570289968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468742 | TCCTAGCCAGATGCA[A/G]TGGCTGACACCGTAA | 58513 |
rs570354280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469377 | CAGCCACAGGGCACC[A/G]GGGTTAAGGACGGAG | 58513 |
rs570370341 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463725 | ACCATCAATCAACCC[C/T]GCAAAGAGAAAATTA | 58513 |
rs570377807 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375971 | GAGCTGGGGGCATGC[A/G]GAGCCTGCTAGGTCC | 58513 |
rs570387878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416978 | CAGACCTGGAGGCCC[C/T]TTCACACCTTCAGCT | 58513 |
rs570424821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365080 | AAGGCACTCCCAACT[A/G]GAATGCCATCACAGG | 58513 |
rs570426744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373477 | AAACGTTGGACTTTA[C/T]GCTTAAAAAAAAAAA | 58513 |
rs570457190 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398183 | CGGTCTGGGCTGTGA[A/G]TGAGTGTGAATCAGC | 58513 |
rs570485183 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401101 | TCGTTTAAATTTAGA[C/T]GATAAAGCTGATGAT | 58513 |
rs570508247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383811 | TGCTCAGAGACTCAT[C/G]TGCTCCACCAGCTGA | 58513 |
rs570526749 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473828 | GCCGGTTGTGGTGGT[A/G]GGCACCTGTAATCCC | 58513 |
rs570551639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396535 | TCCCAACGTACTGGG[A/G]TTATAGGCATGAGCT | 58513 |
rs570571595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449160 | ACACCTGTAGTCCCA[G/T]CTACTCAGGAAGCCA | 58513 |
rs570575215 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458536 | TTCACCCGCTTCCCC[A/G]CTGCACCTCGCACAC | 58513 |
rs570628419 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367351 | ACAGGGGGCAAGGGA[C/T]ACAAGACTGAAGAAA | 58513 |
rs570651399 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435436 | GCTTCCAGTCTGTTC[C/T]ACCCTCCAAAGGAAA | 58513 |
rs570652875 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428107 | TTGGGAGGCTGAGGC[A/G]AGAGAACTGCTTGAA | 58513 |
rs570678995 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435073 | CTCAGCACTCGTACC[-/T]CCCGAGTAGCTGGGA | 58513 |
rs570679170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458981 | GCAGCGCCTGCTCCA[C/T]GCCTGGGCTGTGGTC | 58513 |
rs570685134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370877 | GGGGGCGTGGGCAGG[A/C]AAGAGGGACTCCACC | 58513 |
rs570721588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371611 | TAGCGGTAGAACTGC[A/G]CTGGCTGGTGTCACC | 58513 |
rs570743440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357643 | AGATGTGGCAGTGAG[A/G]GGGATGCGGGGCCCT | 58513 |
rs570751591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378778 | TGAGGGAAGGGGCTG[A/G]GGTGTCCCAGGAGGG | 58513 |
rs570770879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453741 | AAAAAATGACTTATC[A/G]GGTACTATGTTCACT | 58513 |
rs570787942 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372740 | GTCACCGTGCAAGGC[A/G]CTTCACCCACACACC | 58513 |
rs570859616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364303 | GGAGACCCTTCCCTA[C/G]AGGGGCAGTGCCCAG | 58513 |
rs570865941 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472885 | GAGGCTGAGGCCAGA[C/G]AATCACTTGAACCCG | 58513 |
rs570879454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434175 | GGGACTGGGTGAACA[A/C]TGTAAGCCACACCCT | 58513 |
rs570897344 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384420 | GAAGGCACCTCAGTC[A/G]TAAGGGGCTTCTATT | 58513 |
rs570922201 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366623 | AACTGCTGGCCTCTT[C/G]TTTTCAGAAGGAACA | 58513 |
rs570942212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383309 | GCGGTCATTAGATCC[C/T]GGCCCTAGCTCAGGC | 58513 |
rs570951937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376439 | TCCTCAGGGGACCCT[C/T]GAGGGCCAAGGCTAG | 58513 |
rs570959237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363605 | TTAGCTCTGGGCCTC[A/G]GCAAGGGAAAGTGCC | 58513 |
rs570960497 | snp | A/G | 0.00160096 | 0.0282474 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428208 | TCCGTATCAAAAAAA[A/G]AAAGAAAGAAAGAAA | 58513 |
rs570986085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386637 | AGAGGATGGAGCCCA[C/G]AGACAACCACTCCCA | 58513 |
rs570989840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434681 | CCCTGAAGGAAATAA[C/T]GTTATGGCAACCTCG | 58513 |
rs571023164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387507 | AGCTACTTGGGAGGC[C/T]GAGGCAGAAGAATCA | 58513 |
rs571037783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453043 | CTGACCTCATGATCT[A/G]CCCGCCTCGGTCTCC | 58513 |
rs571061709 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402959 | CACTGAAAGTAATCC[C/T]ACAGATATTAACCAT | 58513 |
rs571101949 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416009 | TCTGCTGCACTGAAC[A/C/G]TGAAGTGGGATGCCT | 58513 |
rs571107745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446286 | CAGGGTTCACCCAAC[C/T]CTGATCCCCGCACGT | 58513 |
rs571113288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368462 | GGATGCCCACACAAT[C/T]GTCATTCATCCTGCA | 58513 |
rs571113308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360575 | AGCAAGACCCTACCT[C/T]TACAAAAAAAAAAAA | 58513 |
rs571173075 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357315 | GATACTAGGTGAAAC[A/T]GACAGGGAGGATGCG | 58513 |
rs571246625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361424 | GCAATCTTCTTTTCA[A/T]ACTTCGGAAGTGTTT | 58513 |
rs571253950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437273 | TAACCCACATGTCCA[G/T]AGAGATGAATGGATA | 58513 |
rs571255304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468859 | TCTTCAAAAAAAAAA[C/T]TGTTTAATTAGCTGG | 58513 |
rs571262443 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393658 | CGTCTCAAAAAAAAA[A/T]AAAATAAAAAATAAA | 58513 |
rs571267901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381128 | CCCTGGGCTTCACGC[C/T]GCCCTCTGAAGCTGC | 58513 |
rs571278210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461038 | GGGCCAGGCGCGGTG[A/G]CTCACGCCTGTAATC | 58513 |
rs571331529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432227 | TCACCTGAGGTCAGG[A/G]GTTCAAGACTAGCCT | 58513 |
rs571357371 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402786 | GATGGGGTCTCGCTA[C/T]GTTGTCCAGTCTGGT | 58513 |
rs571369260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443487 | GCCAAGGCAGGCAGA[G/T]CACCTGAGGTCAGGA | 58513 |
rs571414297 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451705 | GTCTAATTTTTTGTA[A/T]TTTTTAGTAGAGACA | 58513 |
rs571429816 | in-del | -/GGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412725 | GGGTGGGGGGGGGGG[-/GGG]TGTCAGAGGCCCTGG | 58513 |
rs571437396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450550 | CAATGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 58513 |
rs571463400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463307 | GACGGTTGCAGACAC[C/T]ATGCCTGCTTCTTCC | 58513 |
rs571507373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379773 | ACAGTGTCCAGTCAC[A/G]CCAGTGCAGAGGTCT | 58513 |
rs571514561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412960 | TTCTCCCGCCCATCA[A/G]GGAATCTGAGATCAT | 58513 |
rs571519868 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430380 | GCCCTGTCCACAGTA[A/G]GACCTCATCCCTTCT | 58513 |
rs571527097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406092 | GGTGGGGCTGAGTCC[A/G]AGAGCCAGCCTGGGC | 58513 |
rs571548065 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443879 | ATCAGTCTGGCCAAC[A/G]TAGTGAAACCCCGTC | 58513 |
rs571548424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424130 | ATCAGACCCTGGTGG[C/G]TGGAAGTGGCTTCAC | 58513 |
rs571611674 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452448 | GAAATTCCATCTCGA[-/A]AAAAAAAAAAAAAAC | 58513 |
rs571624947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385665 | ATGATACCAAACACT[A/G]CTACCCGCCCCACGC | 58513 |
rs571667589 | snp | A/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473709 | CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCC | 58513 |
rs571687287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418810 | GCCATGTGAGGACAC[A/G]GCAAGCAGGTGGCCG | 58513 |
rs571707701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380183 | ATCTAGTCACACAGA[C/T]GTGGCCGTGTAAGGC | 58513 |
rs571739814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374986 | AATGCATGCACATAT[A/G]TAAGCATGGAGGGTG | 58513 |
rs571773050 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407177 | TGCCATGTCAGCGTC[G/T]GCAGTGACAAAGGTG | 58513 |
rs571784445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452780 | AAACCCTTCCCTCTA[C/T]ATCTATTTTATTTTT | 58513 |
rs571799157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359612 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGCCTG | 58513 |
rs571800989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363255 | CAATAATATGCAACA[C/T]GATTCCGGCGTGTTA | 58513 |
rs571851900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398768 | CCTGCTCCGCTTCTG[A/C]CCAGGGCAGGTTTAC | 58513 |
rs571854594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467207 | GCTGGAGTGTGCAGT[A/G]GAGTGATCTTGGCTC | 58513 |
rs571901375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370258 | GGCAGGCAAGGGGCG[C/T]GCTGACTCAGGGCTT | 58513 |
rs571910622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426727 | CTAGATCCCAGGAAA[C/T]GAAAGACAAAAGACA | 58513 |
rs571923955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414640 | TCCTGACCTAGTGAT[C/T]CGCCCGCCTCAGCCT | 58513 |
rs571949194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392508 | GACATAAAAGAACAC[A/G]TCACAGAATGATGCC | 58513 |
rs571987834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384964 | CCCCACGGGACTGCA[A/G]TGCATTGGATCACAG | 58513 |
rs572008648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457821 | TTCCTCTGACCCATG[A/G]GCGGTCTCCCTGGAG | 58513 |
rs572021130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458186 | TGGCCAGGTCAGTGC[C/T]ATGCCACCTTCCTCC | 58513 |
rs572039222 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452543 | GAGGATTGCCTGAGG[A/C]CAGGAATTCCAGGCT | 58513 |
rs572039584 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398796 | TACCTCTCCTTAGGC[A/G]ACTGGTGGTCCCCTG | 58513 |
rs572083152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445879 | TGCAGCAGAGCTGAC[C/T]CGATGTGTTCTCCTG | 58513 |
rs572102312 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381727 | TTAGCTTTAAAATGG[G/T]CCGTTTAGGGTCGGC | 58513 |
rs572117435 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395227 | AAAAAAAAGGCATTC[C/T]TTTCCCCCTCCATTT | 58513 |
rs572145641 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439078 | GTTTTTTTTCTGTTT[G/T]TTTTTTTTTTTATTA | 58513 |
rs572181078 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418444 | GGGCAGGCTCTGATG[A/C]TGCAGGCATGGAGTA | 58513 |
rs572182050 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402545 | CATGTCAGAAAAGAC[C/G]CTTTTTTTTTTTAAA | 58513 |
rs572207024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420427 | GTTGGTTTCTAAAAG[A/G]GACACTGGATCTGAG | 58513 |
rs572209829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420868 | TTGTGCTCACCCTCC[C/T]GCCAGGAGCCAAAGC | 58513 |
rs572231040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381795 | TGTGGGTGCTTCTGC[A/G]ATTCATGGAACATGT | 58513 |
rs572232693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432502 | GAACCCAGGAGGCGG[A/G]GCTTGCAGTGAGCAG | 58513 |
rs572240747 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464023 | AGGCCTGGGAAACAC[G/T]GGGAGCAGGTGTGCT | 58513 |
rs572250384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464570 | CCCAAAGTCCCAGCC[A/G]CATGTTTTGGCCCTT | 58513 |
rs572283595 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376187 | CTCCTGTGGCTGCCC[A/C]CAATTCAGGGACAGT | 58513 |
rs572283943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412826 | GACAGCACCGGAGCC[A/G]GGACCAAGGCCACGG | 58513 |
rs572303370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444787 | GCTGGAGAGCAGTGG[C/T]GCAATCTCAGCTCAT | 58513 |
rs572312407 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395273 | CCTTACTTTTCTAGT[C/T]GAAGAACCACTCTAA | 58513 |
rs572322411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369637 | ACATTTACATAAAAC[C/T]TGCCAGGCAAGGGCT | 58513 |
rs572340322 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364112 | TTGGAGGGCGAGCTG[C/T]CCTGGGCTCTATTAG | 58513 |
rs572343289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413288 | GTAACTCATCCCCAC[A/G]CCCAGGGGCACTGGC | 58513 |
rs572348577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382126 | CACCTCGGGCCAAGC[C/T]GGCTTGGCGCCTCCC | 58513 |
rs572362508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438123 | TTTGGGAGACCGAGG[C/G]AGGTGGATCACCTGA | 58513 |
rs572372135 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355469 | GTCAGCCCCGGGGGG[C/G]ATGGCACAGTGGAGA | 58513 |
rs572399185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401177 | CGAGAAAAGAGAGTA[C/T]GGGAGGAAAGAGGGA | 58513 |
rs572501528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375637 | TCCCTTTGTTGTTTT[C/G]TTTTTCCTCCTGATG | 58513 |
rs572516435 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469816 | CAGATCACAGCCACC[G/T]GCTGCAGGGTGCTTC | 58513 |
rs572521170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429174 | CTCAGCTGGGCAGGG[C/T]TGCGAGCTCATGTCT | 58513 |
rs572556650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387282 | CAGCCTGGACAACAT[A/G]GCAAAACCCTGTCTC | 58513 |
rs572594512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387872 | AATTACTCAATCTGA[A/G]GAAAAAGGAGAAAAA | 58513 |
rs572604853 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414174 | AGGTGGAGGGGCCAC[A/G]TGAGGGGGAACAGGG | 58513 |
rs572627758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368155 | AAGCTGCCCACCTTC[A/G]CTATTATCCTATACA | 58513 |
rs572630352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429639 | TGGCTACCACAGGAA[C/G]TGCTCCAGAACACAC | 58513 |
rs572650916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457116 | GCCTGGGGACTGCAG[A/C]GACTCACAATGCAGA | 58513 |
rs572653248 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384649 | TCCTTCAACAGTTCA[-/CTC]CTCCTCACCTGTGGA | 58513 |
rs572664636 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412975 | AGGAATCTGAGATCA[C/T]TGACTTTTGCCTGGG | 58513 |
rs572679409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409412 | AGAAAACACAGGGAT[A/G]CATCATGTGACCTGA | 58513 |
rs572701743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435030 | CTCACTGCAACTTCC[A/G]ACTCCCAGGTTCAAG | 58513 |
rs572735737 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403351 | GGCTGTGGAGGATGA[C/T]GTCTGTTCTCTTGCC | 58513 |
rs572739379 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444141 | AGAAGGAAAATAGCA[C/T]AAAGATCTGAAAGGG | 58513 |
rs572742178 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410034 | AGCTACTCGGGAAGC[C/T]GAGGCACGAAAATCA | 58513 |
rs572749630 | snp | C/T | 3.50005e-05 | 0.00418319 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441848 | CTGCGGGGGGAGCTG[C/T]GAGGGCAGCCACAGA | 58513 |
rs572770499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368748 | ACAACAGGTGATCCC[A/T]CAAAACCATCATTCA | 58513 |
rs572773247 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404038 | AAGCTAAGCCAGGGA[C/T]GCAGACACCTAACCC | 58513 |
rs572798983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391505 | GAGCCCTGAGAAGGA[A/G]GGTGAGTGCCCGTCT | 58513 |
rs572799979 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433072 | CGCCCCAGCCTCCCA[A/C]AGTGCTGGGATTACA | 58513 |
rs572810540 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435680 | GGGATCCTCTCCTGG[A/C]CATCGGACTTGCTGA | 58513 |
rs572864266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466505 | TCAGCCCCGTGAGGC[A/G]GCACTGCCTTCAGAT | 58513 |
rs572880010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392031 | AAATAAGAACTATGG[G/T]TGACATCCTCCTTGC | 58513 |
rs572902568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370500 | GATGCTGGGGTGGGA[A/G]CCCAGCCACTCTAGG | 58513 |
rs572913890 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473479 | CACCATTGCACTCCA[A/G]CCTAGGTGACAGAGC | 58513 |
rs572998811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384762 | TCGCTGGCCCACTTT[C/T]CCTGGACGCCTCGCA | 58513 |
rs573001724 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365209 | GGTGTGGGGCATGGC[A/G]GCCACCCCCCTCAGC | 58513 |
rs573049639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447478 | ATTTAAGTATTACAG[A/G]GCCAGGCACTCTGGC | 58513 |
rs573068675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357391 | TAGCCAGGATGAAGC[A/G]TGGGGTGGGATAAGC | 58513 |
rs573150099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377451 | ACAGCAGGGGCCCTC[C/T]GGCCTGTGGGTGATG | 58513 |
rs573150739 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448008 | TCAGGAGGAAGGAAA[A/G]CCTTTCCACAAAGGG | 58513 |
rs573153813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471455 | TCCAAGGAGGCAGGG[A/G]ATCAGTCTGAGATCG | 58513 |
rs573159729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422247 | ATCATGGGTCAACCA[A/G]GGCCCGGTCACCTCC | 58513 |
rs573183183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421654 | CTGGCAAAACTGAGG[A/C]TGAGACAGGTTGAGG | 58513 |
rs573195044 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427961 | TAATCCCAGCACTTT[-/G]GGGAGGCCAAGGCGG | 58513 |
rs573214817 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472175 | TCTGCGTCTTCCGTG[C/T]TCTCTTGCCCGTTCC | 58513 |
rs573224685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382806 | CTAAGAGTGCAGGCC[C/T]GAAGAGCCTCCCAAA | 58513 |
rs573245905 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459190 | GGTTATGCGGTGCGT[A/G]ACTGCATTCCCTATG | 58513 |
rs573263768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375363 | GTGCATGCAAGAGCA[C/T]ACACGTGTACGTGCA | 58513 |
rs573275632 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360619 | TTGCGTGGTGTTGCA[C/T]GCCTGTCGTCCCAGC | 58513 |
rs573290091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372215 | CTGTACGCTGTGACC[A/G]GAACTCTCCCTCGAG | 58513 |
rs573374378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453193 | CAGCCTCAACCTCCT[G/T]GACTTAAGGGATCCT | 58513 |
rs573406107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396051 | GGTGGAGGTTACAGT[C/G]AGCTATGATTGTGCC | 58513 |
rs573429705 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390753 | TTAAGTAATCCATAA[A/G]TGAACAGAATTCACA | 58513 |
rs573431941 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453856 | TACAATAAAAAAAGC[C/T]GAAATCCAAGAAAGA | 58513 |
rs573443113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389420 | GATCACACCACTGCA[C/T]TTCAGCCTGGGCAAC | 58513 |
rs573490558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433738 | TTGGGAGGCCGAGGC[A/G]GGTGAATCTGAGATA | 58513 |
rs573497139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464947 | AGCCAGGTGTGGTGG[C/T]GGGTGCCTGTAGTCC | 58513 |
rs573503453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390115 | AAGCAAGCCCCAACA[C/T]TATGCTACTTACAAA | 58513 |
rs573552161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419043 | ACAGTCCCCCACAAC[A/T]AAGCGTCCCCTGCCC | 58513 |
rs573554851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468252 | AGCAACACAGCTAAG[G/T]ATGCTGAGGCTAGAA | 58513 |
rs573558501 | in-del | -/CACA | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458689 | ACACACACACTCACT[-/CACA]CACACTCAGCCACAC | 58513 |
rs573590994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438302 | AGGCTGCAGTGAGCC[A/C]AGATCATGCCACTTC | 58513 |
rs573611825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469034 | CAAAAATCAAAAAGA[G/T]GACTTCCACAGTGGC | 58513 |
rs573631903 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388334 | AATGAGCCACTGAAC[C/T]GGCAATGAAAACTTA | 58513 |
rs573651388 | in-del | CTATCTCA/GAGATTATATCTC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395936 | GGCGATAGAGTGAGT[CTATCTCA/GAGATTATATCTC]AAAAAAAAAAAAAAA | 58513 |
rs573656644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457662 | GAGGGGAACAGATTC[C/T]AGCCCTCCCTCCTGA | 58513 |
rs573661327 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430264 | TCACTGGGCCAAACT[A/G]TGATTATCAGGGATG | 58513 |
rs573663991 | in-del | -/CGAGACCATCCTGCCTAAC | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464876 | ATCACAAGGTCAGAT[-/CGAGACCATCCTGCCTAAC]CAGTGAAACCCCGTC | 58513 |
rs573670092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457151 | CGGAGAAGGAGGACA[G/T]GCCAGTTCCCTAAAA | 58513 |
rs573670539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425445 | GCTCCCAAGCTGACC[A/G]GAGTGAAAAGAAATC | 58513 |
rs573673344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449595 | AAACAACAACAACAA[A/C]AAAAAACTAAACACA | 58513 |
rs573705325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467234 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 58513 |
rs573746983 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460027 | AGGCCTGTAATCCCA[A/G]CACTTTGGAGATTAA | 58513 |
rs573789970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450843 | TCCCCAGAGAATCCA[A/G]GACTCTTCCTTCAGA | 58513 |
rs573814634 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391591 | CACGCTCACTCCATC[A/G]TGAACATCCTCTGCT | 58513 |
rs573836334 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393690 | AAATAAATAAATAAA[A/T]AAAATAAATAAATAA | 58513 |
rs573862639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386034 | GCCTAATGGGCTCAG[A/G]CCAGGATCTGGGTGC | 58513 |
rs573868537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462171 | CAGTTTCCTCATCTA[A/G]AAACAAGCACAGGGA | 58513 |
rs573891753 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408819 | TGAGGAGAGGCAGAT[A/C]GGTCAATGGGATAGA | 58513 |
rs573914163 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461253 | AGCTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 58513 |
rs573937966 | in-del | -/AAAT | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440637 | AAAACATTAAAAGAA[-/AAAT]AAATAAATAAATAAA | 58513 |
rs573950158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367160 | TAGAAACATCTGGGA[A/G]TGATGGCATCAAACC | 58513 |
rs573957557 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411953 | ATCCTCCGGCCTCGG[A/C]CTCCCAAAGTGCTGG | 58513 |
rs573970800 | in-del | -/C | 0.030278 | 0.119257 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403230 | CACGAGAAGCCAGCG[-/C]CCCCCCCCTGGACTG | 58513 |
rs573985080 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454856 | AGCTCTGGGCCAGGC[A/G]TGGTGGCTCACACCT | 58513 |
rs574008213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444448 | AACCTCGTTAGATGA[A/C]AGTGTCCAGCCATCA | 58513 |
rs574037523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442864 | AAGACATCGCTGTTT[A/G]GAGGTCACTTCCCCA | 58513 |
rs574059811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392873 | AGCATGGGCAACACA[C/G]AGAAAAATAAAATAA | 58513 |
rs574117610 | in-del | -/TAATAATAATAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393115 | TAATAATAATAATAA[-/TAATAATAATAA]ACAACGCAGGTAAAT | 58513 |
rs574136276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405794 | GGGGATGGGGACACC[C/T]AAGAAGAGGGCAGAG | 58513 |
rs574152520 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399550 | GCAGGGGTGTGCTGG[C/G]AATCAGTTCTCTCAG | 58513 |
rs574155177 | snp | C/T | 0.000271136 | 0.0116402 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417657 | AATTGAATTCAGAGG[C/T]GAGATCTCTAATTAG | 58513 |
rs574174109 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378289 | TGCCCCAGCTGCCTG[A/G]TTTTTCAGGCTCACC | 58513 |
rs574179648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460658 | CACTCCAGAAGCCTC[A/G]ACCCACAGAGAAAGT | 58513 |
rs574180864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447009 | GGATGCAAAAACATA[C/G]CCCGGAGTAGAGCTT | 58513 |
rs574191082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400108 | TGGGGAGGTCGAGGC[A/G]GGCAGATTGCCTGAG | 58513 |
rs574216139 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420876 | ACCCTCCCGCCAGGA[A/G]CCAAAGCACTGGCCT | 58513 |
rs574218929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410962 | AATATTATTCTGCCA[C/T]AAAAAGGAATTCAAC | 58513 |
rs574240917 | snp | C/T | 0.00482997 | 0.0489046 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440794 | GAATGTGGAAGGAGC[C/T]GTGGAGGTCACCCAG | 58513 |
rs574243433 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418170 | CTGAACCCAAGTCAC[A/C/T]GATCCCTTGCTTTTC | 58513 |
rs574260211 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380691 | CCAGTCACACCGATG[C/T]GGTCGTCTGAGGCTC | 58513 |
rs574285354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366388 | GATCTTCCTCCCTTG[A/G]TTTGGGGGGTTTAAA | 58513 |
rs574289655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420944 | CCAGGCCACTCTGCT[A/G]GAGGCTCCAAGGCCC | 58513 |
rs574289656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427467 | AGCATTTCCTTTGAG[A/T]GTCATGTTGATGCTC | 58513 |
rs574299732 | snp | C/T | 3.4659e-05 | 0.00416273 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421277 | CACCCACAGGCCCCC[C/T]GGAGCCACCCACAGC | 58513 |
rs574324584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363761 | CATAGGCCAGTGAGA[A/G]CCTGGCCCGTAGCCC | 58513 |
rs574385713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379795 | CAGAGGTCTAAGGCT[A/C]CAGTATCTAGTCACA | 58513 |
rs574390387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448455 | GAATCGCTTGAACCC[A/G]GGAGATGGAGGTTGA | 58513 |
rs574417473 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409092 | TGAATTAGCTAGGTG[G/T]GGCAGTGCACACCCT | 58513 |
rs574532348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382665 | GTGAAATAAGTTGGA[C/T]TCTTGTTTTTATTCT | 58513 |
rs574539546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394991 | TTGTGGGGCTGAGGC[A/G]GGTGGATTACCTGAG | 58513 |
rs574614865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415511 | GTGATCATTGGAATA[G/T]TCATTTCCACAAGCC | 58513 |
rs574635384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458821 | AGAGCTCTACTGAAC[A/G]TATCGGGCACCTTTC | 58513 |
rs574646508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376692 | CCTCACCCCCAACAG[A/G]CCCTCCCTGAGCACG | 58513 |
rs574653127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452883 | CTCACTGCAAGCTCC[A/G]CCTCCCCGGTTCATG | 58513 |
rs574675958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370334 | AAAAGCAGGGAGGCG[A/G]TGCCCAGAGCTGCAC | 58513 |
rs574702315 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438910 | ATCCCCTCGGCCTCG[A/C/T]TGAATGGAACATCCC | 58513 |
rs574737027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432524 | AGTGAGCAGAGATTG[C/T]GCCACTGTACTCCAG | 58513 |
rs574762402 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401196 | AGGAAAGAGGGAGGC[A/G]GTGCACCCAGCGGGG | 58513 |
rs574763077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433058 | TCAAGTAATCTGCCC[A/G]CCCCAGCCTCCCAAA | 58513 |
rs574819317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388624 | CGAGGTCAGAAGATC[A/G]AGACCATCCTGGCTA | 58513 |
rs574821967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387965 | CATATCCATGTAACT[A/G]GAATCCCAGAAAGAG | 58513 |
rs574822146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371050 | AGATCATCGTGGGAA[C/T]GAAATTGAAGTAGTT | 58513 |
rs574847250 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357711 | GGGACAGGCGGAGTG[C/T]CAGTATCAAGAAAAG | 58513 |
rs574848357 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360578 | AGACCCTACCTCTAC[-/A]AAAAAAAAAAAATTA | 58513 |
rs574869153 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356729 | AATAAAAACTTAAAA[A/G]AGGGAGAAAACCATC | 58513 |
rs574928366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469843 | CTTCCCTTTTGCCCC[A/C]AACCAAAAATTTTGG | 58513 |
rs574942102 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471637 | GTCCCCGGCCTGGGA[G/T]CTTCAGCGGCGGCAG | 58513 |
rs574942750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470319 | TTGAACTCGGGAGGC[A/G]GAGGTTACAGTGAGC | 58513 |
rs575003702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471013 | TGGAGCCAAGATTTG[A/G]ACACATGATCTGACC | 58513 |
rs575005866 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382180 | CAATTGGCAACTCGC[A/C/G]AGGCGACAGGCTTTC | 58513 |
rs575010444 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473851 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 58513 |
rs575033636 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424212 | GAGCATTGCTGGCCT[C/G]GAGATGAGGAAGTTG | 58513 |
rs575059102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444249 | ACATGAAAAAGCAAG[A/G]AAAGCCAGAGATTTA | 58513 |
rs575059165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451398 | TGGTCTTGTTATCAG[A/G]TAATACCAATACCAA | 58513 |
rs575063676 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431467 | TGCCACCATGCCCAG[C/T]TAATTTTTGTATTTT | 58513 |
rs575087988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429697 | AGCCTGGCAGATGGG[A/G]CCCTGTCACCTGGCT | 58513 |
rs575104755 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422957 | GCAAGACTCCGTCTC[-/G]GGGGAAAAAAAAAGG | 58513 |
rs575126448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438169 | ACCAGCCTGGCCAAC[A/G]TGGCGAAACCTCATT | 58513 |
rs575163664 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398391 | CAAGCACTGCAGCTG[A/C/G]AGACAGTGCTGAGTG | 58513 |
rs575214432 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430397 | ACCTCATCCCTTCTC[C/T]ACCCTTCCACAACTG | 58513 |
rs575242207 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415513 | GATCATTGGAATATT[C/T]ATTTCCACAAGCCCA | 58513 |
rs575260353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445697 | TACTGGGAAAGAGCC[C/T]TCTGTATGCTGAGAG | 58513 |
rs575268131 | in-del | -/TGA | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446763 | GAAAATGCACGTCCG[-/TGA]TGATGACGTGCTGGA | 58513 |
rs575313118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379940 | ACGGCCATCTAAGAC[C/T]CCAGTGTCTAGTCAC | 58513 |
rs575328877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404120 | ACACAAATGAAAAGG[C/G]AGATGGGCTCATCCC | 58513 |
rs575332211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373015 | TGGGTGCCCTGGGAT[A/G]GACAAACCCTGGATG | 58513 |
rs575370234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373681 | GTGTGGCCAGGAACC[C/G]GGAAGGGAATTGTAC | 58513 |
rs575406087 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359196 | CGCTGAAAGAGTCAC[A/G]CTGCCAATCTGCCGG | 58513 |
rs575406529 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467415 | TCAGCCTCCCAAAGT[A/G]CTAGGATTACAGGCG | 58513 |
rs575424480 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435684 | TCCTCTCCTGGCCAT[C/T]GGACTTGCTGACTCA | 58513 |
rs575440698 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404517 | GTTCCCAGGTAACAC[A/G]AGCTCAGGGGAGTCC | 58513 |
rs575471389 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461426 | CAGGAGTTCGAAACT[G/T]GCCTAGGCAACATGG | 58513 |
rs575474323 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472437 | GTGTGTGTGTGTGCG[C/T]GCTAATTTGGGGGAC | 58513 |
rs575486833 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473147 | CAATAGAGTAATGAA[A/G]GTTTTTAACAGTCTT | 58513 |
rs575548141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465822 | AATGAGGTTAGGAGA[C/T]GTCATAAACTTAAAA | 58513 |
rs575555874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377962 | TCTCAAACCCAAATC[A/G]GACCATATCCTCCAG | 58513 |
rs575580241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459781 | TTTACAAAGAATGGT[A/G]GGCGGGGAGGGAGGT | 58513 |
rs575584570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376110 | TGATGGAAAGGGCTC[A/G]GGGGCATGCCCTATC | 58513 |
rs575594049 | snp | A/T | 1.65258e-05 | 0.00287448 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441948 | AAAGCGCAGCTTCAC[A/T]CGCCCCCACCCTCCC | 58513 |
rs575621152 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363677 | ATGAGAAGGAGGGCG[A/C]CAAACAAGGTGACAT | 58513 |
rs575626997 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454287 | GGGGTCCAATCTTCA[C/T]CAGCTTGCTAAATGA | 58513 |
rs575641653 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453951 | TAATGGCACAAGCTG[C/T]GTCAGGTTTAAGTGT | 58513 |
rs575655392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442724 | CTGAGTGCTCAGAGA[C/T]GCACACTGACCAGCC | 58513 |
rs575660287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357149 | CACAGGAACACTCAC[A/G]GCCTCTCCACCACAC | 58513 |
rs575681608 | in-del | -/AAAAGAA | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428594 | AAAAGAAAAGAAAAG[-/AAAAGAA]AAAAGAAAAGAAAAA | 58513 |
rs575686374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365354 | GTAACTGAGTTAAAA[C/T]GAAGTCAAAGGATCA | 58513 |
rs575697383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454538 | GCAGGATCTGAAGGA[A/G]TTTTCATGGATTCTC | 58513 |
rs575704335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422922 | GAGATTGTGCCACTG[C/T]ACTCCAGCCTGGGCG | 58513 |
rs575711036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434341 | ACACTGAGTGCAGAA[A/G]AACCAAGCCCGTGGC | 58513 |
rs575713971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458131 | GTGTTCCTGACAGTG[C/G]GGGGTGGCTCCCTGC | 58513 |
rs575716459 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417092 | AGGGGCTGATGCCTG[A/G]GGCTACTGAGCTGCG | 58513 |
rs575722179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369496 | AACCCAATGGCTGTG[G/T]CCTCATCTTGCCATT | 58513 |
rs575727876 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381792 | GTCTGTGGGTGCTTC[G/T]GCGATTCATGGAACA | 58513 |
rs575759298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370183 | TGGGGGACACTTTTG[C/T]TCTCTTTATGGCCAG | 58513 |
rs575794345 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381266 | TGAGGCACACAAAGG[A/C]GGCGCAGCCTGCCCA | 58513 |
rs575834958 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456992 | GCCAGCAAGGTGGGC[A/G]CATATGCATATGAGA | 58513 |
rs575864755 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469232 | GCTCCAGGGGAGGGA[C/G]CGCACAGAGAGATAA | 58513 |
rs575878120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391102 | AAATTGAACCATCGT[A/G]AGTCAGGGACCGCCA | 58513 |
rs575914347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384145 | TCTGCAGGTGGAACT[C/T]GTGAGGAAAGCAGGC | 58513 |
rs575954499 | in-del | -/TAAATAAAT | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432590 | AAATAAATAAATAAA[-/TAAATAAAT]TACAAATACAAATAC | 58513 |
rs575991675 | in-del | -/AAAG | 0.00597723 | 0.0543405 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428208 | CCGTATCAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 58513 |
rs576021536 | snp | C/T | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402428 | CCTGGTCATACTGCT[C/T]CAGGCTCCTGTGGGC | 58513 |
rs576040015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422319 | GCCCCTTCCGTGGCC[C/T]ACTCCACCTGCATTA | 58513 |
rs576061831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407150 | GGCAAGCCAAATGGA[A/C]TAAGACACACATGCC | 58513 |
rs576107384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420371 | TAACCAGGAACTGTA[A/T]GTGTGTTGGTTTCAG | 58513 |
rs576107992 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415642 | CTCCCCGAATCAAGG[A/G]CCACTCTCAGAGCCA | 58513 |
rs576117586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414203 | GGGCAGTGTCCAGGA[A/G]CATGGAGTGGCCCTG | 58513 |
rs576177448 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432482 | CTGAGGCAGGAGAAC[C/G]GCGTGAACCCAGGAG | 58513 |
rs576223559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424755 | AACCTCCGTCTCCCA[A/G]GTTCAAGCAATTCTC | 58513 |
rs576227615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418197 | TTTCAAAAACGACAG[C/T]GACGAAAACAACGGC | 58513 |
rs576230470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386928 | AGACTACAGTCTCTA[C/T]ACAGAACGCTCACCA | 58513 |
rs576236236 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387783 | ACAAACAAAAAAAAA[A/C]CCCACTTCATTAGGT | 58513 |
rs576237640 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418952 | TATGGCACTTTGTCA[C/T]AGCAGCCCAATGGTC | 58513 |
rs576254387 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381439 | AGGCTGGAACCCCAA[A/C]CCTGCCACCTACTCA | 58513 |
rs576265606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381393 | CCCAGTGGTGGGTCC[A/C]GGGCCTCGTCCTGGG | 58513 |
rs576275209 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381730 | GCTTTAAAATGGGCC[G/T]TTTAGGGTCGGCTGT | 58513 |
rs576295310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426086 | ATGAGATGAACTGAG[A/C]ACAGAGGGAAAAAGA | 58513 |
rs576372452 | snp | A/C/G/T | 0.0003202 | 0.0126492 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361759 | AGTGGGGTGGCCCGG[A/C/G/T]GGCGGAGGACTCAAC | 58513 |
rs576382946 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396320 | AGGTTGGAGTGCAGT[C/T]GCACACTCATGGGTT | 58513 |
rs576440452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419664 | AAAGAGAGCTGGGAC[C/T]GTTCTAACAGACTTA | 58513 |
rs576509278 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355349 | CGTGGGAGGGCGGGT[A/G]GGGATGTCTGCAGCT | 58513 |
rs576510522 | in-del | -/CA | 0.00170068 | 0.0291296 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432588 | ATAAATAAATAAATA[-/CA]AATACAAATACAAAT | 58513 |
rs576529682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455544 | CTTCAGGAGAGACTG[C/T]CCAGCTCCATCTACA | 58513 |
rs576546866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398953 | GGCACTCGCCACCAT[A/G]CCTGGCTCTATTTAG | 58513 |
rs576572053 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393517 | AGCCGGGCGTGGTAG[C/T]GGGCGCCTGTAGTCC | 58513 |
rs576572240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400614 | GTATTTATTAAGAAA[C/T]AGAAACAAGCCAGAA | 58513 |
rs576614027 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393695 | AATAAATAAATAAAA[A/T]AAATAAATAAATTAG | 58513 |
rs576618416 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370093 | AAGCTGGTTAGGGGT[C/T]GTGCATGAAAGGACC | 58513 |
rs576635312 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463973 | TGACAGAAAGAGGGG[C/T]CAGGGGGCCACAGAG | 58513 |
rs576666711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456327 | GAACTCGTGCTAAGA[C/G]GCAGCACTGAGGATA | 58513 |
rs576699971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409244 | TAAAAACAAATTTTT[A/T]AAAGTAAAATAATAA | 58513 |
rs576739714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461973 | CCAGCCTACTATGTG[C/T]CAGGAGCCCAGATTT | 58513 |
rs576774702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358683 | CGATGGGATGGCCCC[A/G]GGAGGCGCCCGGCAC | 58513 |
rs576798385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367244 | TGCAGCGGGAACTAC[C/T]GGGGACCACAGCAGA | 58513 |
rs576806551 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375217 | ACATGCAGGCACATG[A/C]GAGAATACTCATGTG | 58513 |
rs576807167 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422108 | GCAGCCCCAACCCCA[C/T]CAGGGCAGATGGAGC | 58513 |
rs576815553 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453397 | GGTGTGAGCATGCCC[A/G]GCCATCAACTTTTAA | 58513 |
rs576838105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397499 | AAGAGCCACTCAACA[A/G]CAGCAGCACAGGCCT | 58513 |
rs576844715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368064 | TGTACTTGGAAAATG[A/C]AGTTCTGCAGATGAG | 58513 |
rs576869720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389200 | GACTCAAGCCTGTGA[C/T]CCCAGCACTTTGGAG | 58513 |
rs576887955 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473260 | TTGAGCCAGGCTCTG[C/T]GGCTCACACTTGTAA | 58513 |
rs576921836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377863 | CATGCCCACGCCACC[C/T]CCACTGGGCTCTGAC | 58513 |
rs576964965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422184 | ACCCGCTGCACGTGC[A/G]ACCCCTCTCGCCACC | 58513 |
rs576978655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390332 | AATCATAAACACCTA[C/T]GCACCTGACAAAGCT | 58513 |
rs577045797 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453161 | CTAGAGTACAGTGGT[A/G]CCATCATAGCTCACT | 58513 |
rs577063287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371268 | CAGGGCTTCCTCGGT[G/T]GCTGCATCCTGTGTG | 58513 |
rs577104394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447274 | TCTCTCCAACTGCTC[C/T]ATCAGAGGTTTCTAC | 58513 |
rs577124423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395909 | GAGATTACGCCATTG[C/T]GCTCCAGCCTGGGCG | 58513 |
rs577147026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470309 | GGAGAATCACTTGAA[C/T]TCGGGAGGCGGAGGT | 58513 |
rs577199509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363936 | CGGAGACAAACTCCC[C/T]TGCAGCCCACCCTTG | 58513 |
rs577207005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382202 | CAGGCTTTCAATAAA[C/T]GCCTGGCACTGCCTC | 58513 |
rs577269419 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433689 | GAAATAAAAAAGCCC[A/G]GGTGTGGTGGCTCAC | 58513 |
rs577280202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377308 | TTAAAACAAAGGTGA[C/T]GGATGTCCACTGAAC | 58513 |
rs577300085 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360721 | CCAATGCAGACCAGG[A/C]TGGGCAACACAGCGA | 58513 |
rs577321336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445800 | AGGGGACGCACCAGG[C/G]GATGAGGCCTGCACC | 58513 |
rs577331107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363217 | ATTCAACGTGGTCCA[C/T]GCAGCACCCCAGACT | 58513 |
rs577337191 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358167 | ACAGTGTCACTGAAG[C/T]GCCTTCCCTTGACGG | 58513 |
rs577351233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407817 | AAAATGTCATTGCTC[C/T]GTCAGGCCACAGCGC | 58513 |
rs577366898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, missense | EPS15L1 | GRCh38.p7 | 19:16356942 | ATTAATGTCTCTCTG[C/T]GATGCACTGCCTCTG | 58513 |
rs577381851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359801 | CAGGAGGTCAAGGCT[G/T]CAGTGAAGCTGTGAC | 58513 |
rs577394315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401913 | GGAAACACACATACA[C/T]ATAGACACATGCCCC | 58513 |
rs577411255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464906 | TAACCAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 58513 |
rs577478155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392774 | ATAATAATATCCTGG[C/T]CAGGCACAATGGCTC | 58513 |
rs577490630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470461 | GCTTAGTGCTTTCTC[A/T]TGAAATGATCTTAGG | 58513 |
rs577498727 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359059 | GTTCTGGAGAGGCAC[C/T]GCCGGGGCACCACCT | 58513 |
rs577515501 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393451 | TCAAGAGTGTGAGAC[C/G]AGCCTGGCTAACACG | 58513 |
rs577517420 | snp | A/C | 8.24654e-05 | 0.00642074 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385188 | AGGACCCACTTCCGA[A/C]GGGATCTAAGGTTCC | 58513 |
rs577581299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457261 | GTGGAGGTGAACAAC[A/G]GGACATTCCCCACCC | 58513 |
rs577631042 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418974 | CCAATGGTCTAAAAC[A/C]CTCCTCTTGTGCCCA | 58513 |
rs577658177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439843 | AAAATGGCCATCTAC[A/G]ACCACTTAAAATCAC | 58513 |
rs577670774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439646 | CAGTAAGCAGTGATC[A/G]CACCACTGCACTCCA | 58513 |
rs577684430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375305 | AGGTGCATGCATGCA[C/T]GTGTCTGCAGGCGTG | 58513 |
rs577694824 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459234 | CCTGCTGCAGGCCAA[A/C/T]GCCCTGCTCTAAGAT | 58513 |
rs577721532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442769 | GCTGGCCAGTAACTG[C/T]TCCCACCAGGGAAGG | 58513 |
rs577741913 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378047 | GGTGGGTGGGCAGAT[A/G]GATGGAATGGTAGTT | 58513 |
rs577750457 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398431 | TGCTGACGACCACAA[G/T]ACACACACGCCCAGC | 58513 |
rs577755455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405385 | GCCCGGTGGGATGTG[C/T]GAGTGTGGGAGGCGG | 58513 |
rs577793625 | snp | A/G | 0 | 0 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399407 | GCCCTTGGCAGAGAT[A/G]TAATATCTTGAACAA | 58513 |
rs577808642 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464107 | GGAGAAGTGACTTTA[C/T]GTCAGCCTGACCTGC | 58513 |
rs577812664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462038 | CAGAGCTCCTCGACC[C/T]TCCCGGAGCCCATGG | 58513 |
rs577909114 | in-del | -/AAAG | 0.00438769 | 0.0466326 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427900 | CTCCGTGTCAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 58513 |
rs577914258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459976 | AGCTCCCAACATCTA[C/G]GATAGAACAATATTT | 58513 |
rs577924172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373849 | GACTGTTAGAGGTTA[A/G]TACGGAATCACAGCA | 58513 |
rs577926736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460436 | GCATTAAATGTGAAT[C/T]AAAGGACATTTTCTA | 58513 |
rs577957390 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461672 | TTTCTACAGATTGGC[A/G]TAATGACAGAGGCAC | 58513 |
rs577995423 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410200 | ATATAAAAGGGCAAG[A/G]AATCGGAATGATTTT | 58513 |
rs578015156 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438174 | CCTGGCCAACATGGC[A/G]AAACCTCATTTCTAC | 58513 |
rs578018924 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427128 | GATAAAACAAATGTA[-/G]GAAATTAGTGACACT | 58513 |
rs578022477 | snp | G/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436950 | ACCCTCACAGCCCAG[G/T]GGGCCTCTGCAGAGG | 58513 |
rs578063473 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453952 | AATGGCACAAGCTGC[G/T]TCAGGTTTAAGTGTG | 58513 |
rs578090429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404157 | GCTAACGGAAGATCA[C/T]TTTGGAATAATGAGG | 58513 |
rs578111448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422953 | ACAGAGCAAGACTCC[A/G]TCTCGGGGAAAAAAA | 58513 |
rs578125935 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429578 | CCTCACCAGCCCACA[A/C]AGCCAAGAGCCTCCA | 58513 |
rs578137276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465937 | TGCCTGAGCTCACTG[A/G]GTACAAACTTGGGCA | 58513 |
rs578151724 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473879 | CAGGAGAATCACTTG[A/C]ACCTGGGAGGCGGAG | 58513 |
rs578154245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429260 | TCAGGCCACTCAGTG[C/T]GCTGAAGAGAAGGCA | 58513 |
rs578162534 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458638 | CCTGAAAGTGCTCCC[C/T]GGCCATCTCCTACCT | 58513 |
rs578201627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373231 | CGACCGCCAGGCTCA[C/T]AGGGGGTCGCATTTC | 58513 |
rs578206036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379178 | GTCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAACT | 58513 |
rs578234651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384201 | CCATCTGCCCCTGCC[C/T]GGGGGCTGCCGAGAA | 58513 |
rs745309076 | snp | C/T | 9.89985e-05 | 0.00703487 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418059 | CATAGCTAACGCGAA[C/T]TGGTCTTTGCTTAAC | 58513 |
rs745374148 | snp | G/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400847 | CTTGCAAACTGCCAC[G/T]TCACTGCCAACTTTT | 58513 |
rs745378633 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379963 | CTAGTCACATAGACG[C/T]GGCTGTCTGAGGCTC | 58513 |
rs745378701 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368791 | CAGACACCTATGCAA[C/T]TGTCATTCACCCTAC | 58513 |
rs745380188 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440455 | TAAAAAATAACACCA[A/G]TGTTATTTTCTGGCT | 58513 |
rs745396854 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469330 | GAAGACCGACGGGCT[A/C]CAGTGTTGCGGAGTT | 58513 |
rs745397753 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444722 | TGAAGCACATTTCCA[C/G]ACAAGTTTTTTTTTT | 58513 |
rs745405199 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409375 | ACCTACATGGAAAAG[C/T]GAAAACTATAAAACT | 58513 |
rs745463018 | snp | C/G | 4.94262e-05 | 0.00497098 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421426 | GGTCTTCAGGAATAT[C/G]TCATCAAATCGCATC | 58513 |
rs745494969 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403814 | CTGAATGCTCTGCTC[C/T]AGCTGGGTTTCCTCC | 58513 |
rs745503180 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379260 | CAGTGAGCTGAGATC[A/C]CGCCACAGCAGCACT | 58513 |
rs745534131 | snp | A/G | 1.66302e-05 | 0.00288355 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441904 | TACCTTCCCAAGGAT[A/G]ATGTCCGAGAGGCCA | 58513 |
rs745565368 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420459 | CAGCTGAGACCCACT[A/G]TCCCTAGCCAGTTGG | 58513 |
rs745565421 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431462 | GAGTGTGCCACCATG[C/G]CCAGCTAATTTTTGT | 58513 |
rs745576769 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405502 | CCACTTCCAAGAAAA[A/G]CATCCTGGAAGCATA | 58513 |
rs745599467 | snp | C/G | 1.64732e-05 | 0.0028699 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393942 | GGTCCGGGAAACACT[C/G]AATTTTACCTGTTGA | 58513 |
rs745604551 | snp | C/T | 2.15352e-05 | 0.00328134 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386271 | GTAAAAAGCAGTTCG[C/T]TGGTTCCATCACCCA | 58513 |
rs745610786 | snp | C/T | 1.68091e-05 | 0.00289901 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404776 | TTGCAGGGGTTTACG[C/T]GAGGATGGGAAAAAT | 58513 |
rs745625434 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376279 | GAACAGGCAATGACC[A/G]GGTAGATAAATGGAT | 58513 |
rs745633772 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375892 | TTCTAAAAATAACTT[-/C]CCCTATGTTCACCTC | 58513 |
rs745655689 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429403 | GCCAACGCTGGGCAG[A/G]CTGCCAGTCCCCGGA | 58513 |
rs745674079 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460017 | ATGGTGGCTCAGGCC[A/T]GTAATCCCAACACTT | 58513 |
rs745762667 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427662 | TTTAGGAGGCAGAGG[C/T]GGGCAGATCACTTGA | 58513 |
rs745765839 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358242 | GCCTTCAGAGTCGAC[C/T]GGTTCAAGGCCAGCT | 58513 |
rs745786905 | snp | C/G | 3.39934e-05 | 0.00412256 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434514 | AAAGAAATAGCCCGA[C/G]TAAGTAGGAGAGCAC | 58513 |
rs745791788 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359353 | GATCGGCTGAGCCCC[C/T]GAATGCCGTGAACAT | 58513 |
rs745791870 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399885 | AGCATGCCACTGGGT[A/C]TGGATGTGACAGATC | 58513 |
rs745813447 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389636 | TTTTCCTCTTTCTTT[A/G]CAATACCCACAATGG | 58513 |
rs745835255 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453579 | TTAGCCCAGCGTGGT[A/G]GCAGGCGCCTGCAGT | 58513 |
rs745846994 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398757 | GGGAGTTTTGACCTG[C/T]TCCGCTTCTGACCAG | 58513 |
rs745848856 | snp | A/G | 3.44727e-05 | 0.00415152 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377093 | CGGCACCGGTAGGCG[A/G]TGGCTGCGAGAGAAG | 58513 |
rs745881140 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466262 | AGTGATCTGCCCCTC[C/T]TGCCCCTATACACTG | 58513 |
rs745893514 | snp | A/G | 8.25852e-05 | 0.0064254 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440795 | AATGTGGAAGGAGCC[A/G]TGGAGGTCACCCAGC | 58513 |
rs745893933 | snp | A/G | 3.30879e-05 | 0.00406729 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403713 | CTGGCATGTGGCAGG[A/G]ACCCGACTCCGTGAA | 58513 |
rs745950994 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365556 | AGATAGAGCAAGTGT[A/G]AGCAGGGAGCCACCA | 58513 |
rs745966861 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386123 | TGCGGGGGAGCTCTG[C/T]TACTGCCCAAGGAAT | 58513 |
rs745967296 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393761 | TGCGGGCAGTGACTG[C/G]ACCTGGGGAGGGGAG | 58513 |
rs745974788 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409922 | CAGCCTGGGCCACAG[A/C]GTGAGACTCTGTCTC | 58513 |
rs745995636 | in-del | -/ACAATGGA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434025 | ATTCCCACATTCAGC[-/ACAATGGA]ACAATGGAAAGGGGG | 58513 |
rs746030467 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405830 | TCACCTCCTGATTTT[C/T]AACCACGCAAATGCA | 58513 |
rs746041930 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435682 | GATCCTCTCCTGGCC[A/G]TCGGACTTGCTGACT | 58513 |
rs746159746 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418056 | ATACATAGCTAACGC[A/G]AATTGGTCTTTGCTT | 58513 |
rs746160727 | snp | C/G | 1.65993e-05 | 0.00288086 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425116 | GTGCTTGGGGGACAG[C/G]CTCCCTGTGCTGTTG | 58513 |
rs746176733 | snp | A/C | 2.20811e-05 | 0.00332266 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428761 | CACTGAGGTCCCAGA[A/C]CTGCAAGGGAGAGAC | 58513 |
rs746191735 | snp | C/T | 1.65985e-05 | 0.00288079 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417538 | TGTGGAGGGAAGGGC[C/T]GTTTCCAACATACCT | 58513 |
rs746206561 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445153 | GCTCTACTTCCCAGG[C/T]GCTAATGAGCAACAA | 58513 |
rs746221595 | snp | C/T | 1.67287e-05 | 0.00289207 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361893 | CTTTTTACTTTGGAA[C/T]GGGTCGCCGCTGTCA | 58513 |
rs746245295 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414151 | CAGAGCGCCCTTGCT[A/G]ACTTTGAAGGTGGAG | 58513 |
rs746276772 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456648 | GGGTGACAAGAGTGA[A/C]ACTCCATCTCAAAAC | 58513 |
rs746314859 | in-del | -/CA | 1.71176e-05 | 0.00292549 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434526 | GAGTAAGTAGGAGAG[-/CA]CACACCTGTGTGAAT | 58513 |
rs746322375 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412634 | CTCTATTTGGAAAAA[A/T]ATATATATATATATT | 58513 |
rs746353451 | snp | A/C/G | 6.78741e-05 | 0.00582521 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417658 | ATTGAATTCAGAGGC[A/C/G]AGATCTCTAATTAGC | 58513 |
rs746355559 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420023 | GCTGACCCGTACGGT[A/G]GCAGCCATCGCAGGG | 58513 |
rs746369621 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371491 | GGGGGCGAAAAGACA[C/T]GCTCATCACCATCAC | 58513 |
rs746422661 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380894 | ATCTGGGCTATTTGC[A/G]TCCCGTCACAGAGAT | 58513 |
rs746436841 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395419 | GATCCGGATGCAACT[C/T]TTGCGTGTTGTTGCT | 58513 |
rs746441140 | snp | A/C | 0.000100393 | 0.00708424 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402462 | CTGGCGGCTTTCATG[A/C]AGCTGGGAAAGTTTG | 58513 |
rs746454136 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379089 | CGGGCAGATCACGAG[A/G]TTAGGAGATCAAGAC | 58513 |
rs746472193 | in-del | -/CT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468128 | GTACAAGGGAGAGAA[-/CT]CTCATTCGGGTGGGG | 58513 |
rs746477777 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367091 | GAGCTTTACTGACGC[A/G]CATTTCAGAAAAGGG | 58513 |
rs746480885 | snp | G/T | 1.68983e-05 | 0.00290669 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434506 | CTAGTTGGAAAGAAA[G/T]AGCCCGAGTAAGTAG | 58513 |
rs746484519 | snp | C/G | 1.69135e-05 | 0.002908 | missense, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361972 | CCAAGCTGGCTTACA[C/G]GTGTACTTTTACCTG | 58513 |
rs746497083 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463999 | CAGAGCAGAGGGAAT[C/G]AGGACTGCAGGCCTG | 58513 |
rs746502469 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420152 | AGACTTCTTTTCTCA[C/T]GGTTATTCAAGAGCC | 58513 |
rs746527036 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420671 | TTTCCTTTTGATAGC[C/T]CCCAAGTGAAGCCTT | 58513 |
rs746530561 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378419 | TCAGGTCTCCTGCTG[A/G]GGAACTCGGCCCACC | 58513 |
rs746558308 | in-del | -/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376401 | CGAGAGAAATCCCAC[-/GT]GTGAGTTAAAGGGCT | 58513 |
rs746582026 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462459 | AGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 58513 |
rs746626967 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471562 | GCTGGGCCGCCGCGC[C/T]GACAGAAACGCTCGC | 58513 |
rs746633014 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432728 | GTGAGCTGAGATCAT[A/G]CCACTGCACTCCAGC | 58513 |
rs746634534 | snp | C/T | 1.65798e-05 | 0.00287917 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417969 | GGGCGTGCCTCTCTC[C/T]GAAGGCGGGACCATG | 58513 |
rs746644493 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388199 | AAGTGTGCACCACCA[C/T]GCCTGGCTAATTTTT | 58513 |
rs746695724 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387158 | CTTAGAAGAGAAATA[A/G]AAAATATACGAAAGA | 58513 |
rs746701967 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402531 | CAGGGTCAGGAAAAC[A/G]TGTCAGAAAAGACGC | 58513 |
rs746723829 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409254 | TTTTTTAAAGTAAAA[C/T]AATAAAAACAATGGT | 58513 |
rs746738921 | snp | C/G | 4.95242e-05 | 0.0049759 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403720 | GTGGCAGGGACCCGA[C/G]TCCGTGAAGTACCTG | 58513 |
rs746749583 | snp | C/T | 3.33256e-05 | 0.00408187 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421506 | GGCAAAACAGTTAAT[C/T]TGGAAGCTTTTTATG | 58513 |
rs746807689 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382949 | GGGAAAAGTTGATGA[C/T]GGTTTTTTTTTGTTT | 58513 |
rs746827780 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404658 | TTGGCCTTCTGCTGG[C/T]CCATCTCGTCCAGGC | 58513 |
rs746855557 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398572 | GAATGTATTTGTTCC[A/C]GAAGAAAGAGAGGAA | 58513 |
rs746862185 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357283 | GACTTTTTCCCCCCC[A/G]GGCCTGTGGGGAGCA | 58513 |
rs746867171 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397470 | AACTTGGAAATGCCA[C/T]GAAGAAAACTGTAAA | 58513 |
rs746892169 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439842 | CAAAATGGCCATCTA[C/T]GACCACTTAAAATCA | 58513 |
rs746917270 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356605 | GTGAGCCACCGCACC[C/T]GGCTCTGAGGGTCAA | 58513 |
rs746945115 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438778 | CTCCTGCCTTAGCTT[A/C]CTGAGTAGCTAGGAT | 58513 |
rs746945528 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431852 | ATAAAAATAATGAAA[C/T]GCAAAATAAAGCAAA | 58513 |
rs746964476 | snp | C/G | 0.0003906 | 0.0139695 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471908 | CAGGCCCGCCCGGCC[C/G]GTACCTGCTGGGAGA | 58513 |
rs747004001 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387586 | CACTGCAGCCTGGGC[A/C]ACAAGAGTGAAACTC | 58513 |
rs747041349 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364000 | GGTTCCACCGGGGTC[A/G]CCGTTGCATCCTTAG | 58513 |
rs747098421 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376164 | CATGATCCTGGGAGT[A/G]CGTGGGTCTCCTGTG | 58513 |
rs747098502 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363042 | CAGTGCATCCTGCCA[A/G]TGTACCAGAACATTC | 58513 |
rs747114601 | snp | C/T | 1.65433e-05 | 0.002876 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385082 | CACCATGACAAGAGG[C/T]ACAAAGACACTAGCA | 58513 |
rs747133817 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447624 | AATTAGCCAGGCATG[A/G]TGGCAGGTGCCTGTA | 58513 |
rs747135758 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459754 | ATTCCTGAGACAGGG[A/G]AGCAGGCCGTATTTA | 58513 |
rs747171364 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437808 | AATTCAGATTGCTCA[A/G]GGTAACTTCATGGCC | 58513 |
rs747186763 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403647 | AAGTAACAAGGGTGA[C/G]AGCAAAGGAGTTCAG | 58513 |
rs747226947 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375387 | ACGTGCACATACATG[A/C]ATAAAAATACATGGC | 58513 |
rs747251195 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421366 | CGAGTGCATGAAGAT[C/T]TCCTTCACCTCCTGG | 58513 |
rs747281785 | snp | A/G | 4.94458e-05 | 0.00497197 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392311 | CCACTCACCTTCGAA[A/G]GTAAGGAAGGGTTTT | 58513 |
rs747292482 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427386 | TCTGAATTTCTGAAT[A/G]TGTGTATTACACTTA | 58513 |
rs747316111 | snp | A/G | 1.65468e-05 | 0.00287631 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440773 | TAGTAATACTTGACA[A/G]TGGAGGAATGTGGAA | 58513 |
rs747332101 | snp | A/G | 3.475e-05 | 0.00416819 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425240 | GTCTTCTTTCTCTTG[A/G]AGGGTGGGATGAGGG | 58513 |
rs747333026 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455537 | TAAACGTCTTCAGGA[A/G]AGACTGCCCAGCTCC | 58513 |
rs747366519 | in-del | -/AAC | 1.68077e-05 | 0.00289889 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425328 | TGGCCTGCAGGTGCA[-/AAC]AACAATGGCACTGAA | 58513 |
rs747369495 | snp | A/G | 1.81105e-05 | 0.00300914 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361809 | AAAGCCCGAGGCAGA[A/G]GCCTTAGAAGGTTTA | 58513 |
rs747395463 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401930 | TAGACACATGCCCCT[C/G]AGATGTCCCCTGCCC | 58513 |
rs747406251 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369892 | CCCATCCTCTGGGGG[A/G]ATTTCCAGGGAGAGA | 58513 |
rs747429315 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465879 | AAGACAAGAAACTAT[C/G]GTGCAATGAAGAGGC | 58513 |
rs747504263 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380127 | GGCCGTCTAAGGCTC[C/T]GGCATCTAGTCGCAC | 58513 |
rs747509723 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422551 | GTGGCTGGAGGGATC[A/G]ATTGTTCCTTCTCCA | 58513 |
rs747517317 | in-del | -/AT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412634 | TCTATTTGGAAAAAT[-/AT]ATATATATATATATT | 58513 |
rs747553465 | snp | C/G | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392418 | TGGGTCACTTTCTTT[C/G]AAAGGGTCCCCTCCA | 58513 |
rs747563429 | in-del | -/AGG | 1.64846e-05 | 0.0028709 | cds-indel, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377224 | ATCCTGCCCCTCCCA[-/AGG]AGGAGGTGAAAGGGC | 58513 |
rs747571256 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464973 | AGTCCCAGCTACGCA[A/G]GAGGCTGAGGCAGTA | 58513 |
rs747573768 | in-del | -/CCACCATCCAAGAGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422045 | GTAACAAATGAGACA[-/CCACCATCCAAGAGGG]CCACCATCCAAGAGG | 58513 |
rs747618078 | snp | A/G | 1.67273e-05 | 0.00289195 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417524 | GTGTAACATCTGGAT[A/G]TGGAGGGAAGGGCCG | 58513 |
rs747692461 | snp | A/G | 1.6693e-05 | 0.00288898 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361899 | ACTTTGGAACGGGTC[A/G]CCGCTGTCAGCCCCG | 58513 |
rs747722776 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359732 | CCAGATGTGGTGGTG[C/T]GCGCCTGAGGTCCCA | 58513 |
rs747723919 | snp | A/C | 4.94222e-05 | 0.00497078 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393930 | AGTCTAAAGACCGGT[A/C]CGGGAAACACTGAAT | 58513 |
rs747728060 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387002 | TGACCACCTCTCACC[A/G]GAAAAGACAATCAGT | 58513 |
rs747741640 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401417 | AGAGGAATCCATGAC[A/G]TACAGAGGCCCAGGA | 58513 |
rs747745065 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430031 | CCAATGTCCCCTGGG[G/T]GGTGGAAGTGTCCAG | 58513 |
rs747748033 | in-del | -/GGAGAGAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428467 | AGGGAGACAGAGAGA[-/GGAGAGAG]GGAGAGAGGGAGAGA | 58513 |
rs747750618 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360378 | ACCCCCAGTGCGCAT[C/T]TAGGGTCAACAAAAT | 58513 |
rs747772048 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443323 | TAAAACCAGGGGGAC[A/G]TAGACTCCTTCCAGT | 58513 |
rs747801498 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372537 | CACGCTTTTTTTAAC[A/G]GAAAAGATTTCCACT | 58513 |
rs747801655 | snp | A/G | 2.33948e-05 | 0.00342007 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428779 | GCAAGGGAGAGACCA[A/G]CATGGGTAACTGTGG | 58513 |
rs747827298 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383948 | TCTTCCAGGTACTCC[C/T]GGGGCTCCCTCCCCT | 58513 |
rs747850262 | snp | C/T | 3.3653e-05 | 0.00410188 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361963 | TCTGCGGAACCAAGC[C/T]GGCTTACAGGTGTAC | 58513 |
rs747856329 | in-del | -/T | 5.42972e-05 | 0.00521015 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437065 | GGTGGGTGGGTTTGC[-/T]TGAAAAGGATACACG | 58513 |
rs747872818 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412046 | TAATACCTAATATAA[C/T]GTAAATGCTATGTAA | 58513 |
rs747897872 | snp | C/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356216 | GGCTCTAAAGCCCCA[C/G]GGCGCAGACAATTCT | 58513 |
rs747902043 | snp | A/G | 0.000115431 | 0.00759618 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437780 | CTCACAAATTTAGGC[A/G]GTGGCATGCTCAAAT | 58513 |
rs747902196 | snp | C/G/T | 5.27601e-05 | 0.00513592 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418156 | GGCGCCGACTCAGCC[C/G/T]GAACCCAAGTCACCG | 58513 |
rs747940312 | snp | A/T | 1.65471e-05 | 0.00287633 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377296 | CAAAAATAGTTGTTA[A/T]AACAAAGGTGACGGA | 58513 |
rs747947867 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366965 | ATAGCTTATCTCAAA[C/T]GTGACAAAGTAACTT | 58513 |
rs747955644 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411393 | CTCACTGAAAGAGAA[C/G]AGTTAACGATGAATC | 58513 |
rs747999971 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451385 | GGAAATGTGAATATG[A/G]TCTTGTTATCAGATA | 58513 |
rs748008667 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381432 | CCTGCCCAGGCTGGA[A/G]CCCCAACCCTGCCAC | 58513 |
rs748051973 | snp | G/T | 1.65362e-05 | 0.00287538 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421341 | GTGCTAGAAGGTTCT[G/T]GGTGAGGCCCGAGTG | 58513 |
rs748076242 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366415 | TAAAAAAAAGAAATT[A/G]GTTTTTGGGAGGAGC | 58513 |
rs748097659 | snp | A/G | 1.69252e-05 | 0.00290901 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403921 | GGATTTGCGTTTTCA[A/G]TGATGAGATCTGAAA | 58513 |
rs748106010 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449935 | ATTCCATCACATAAC[A/G]TCATTAAAATGATAA | 58513 |
rs748137676 | snp | A/C | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434450 | CCATTGATGGGCAAG[A/C]GGCTTTCAAAAATCC | 58513 |
rs748160534 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446311 | GCACGTGGCCGAGGG[C/T]AGGACGCCTCCTACA | 58513 |
rs748168085 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377684 | CTGGTGTGCCGCCTC[C/T]CCACTGAGCTGGCCG | 58513 |
rs748203322 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415945 | ACATCCTTGCTGATC[A/G]CCAGTTTGGATAACA | 58513 |
rs748219359 | snp | C/G | 1.86291e-05 | 0.00305192 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361800 | GAAGTCTGCAAAGCC[C/G]GAGGCAGAGGCCTTA | 58513 |
rs748237514 | in-del | -/TGTA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369706 | GTGTGTGTGTGTGTG[-/TGTA]GGGTGGGGTATGTGA | 58513 |
rs748246922 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384032 | GGGGACCCCCCACAC[C/T]GGCCACCCCTTACCA | 58513 |
rs748259491 | snp | A/G | 1.65132e-05 | 0.00287339 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395494 | TGAAGAAACAGGACA[A/G]GGATTTTATTATTTC | 58513 |
rs748267164 | in-del | -/AGAA | 0.000105868 | 0.00727481 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362013 | GAGAAAAAAAAAAGG[-/AGAA]AGAAAGAAATATGAG | 58513 |
rs748273404 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426355 | ATGTCCACGTTGAAA[C/T]CAGGCATGGTGGCTC | 58513 |
rs748349302 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387773 | CTGTCTCAAACAAAC[-/A]AAAAAAAAACCCCAC | 58513 |
rs748357022 | snp | A/G | 6.5937e-05 | 0.00574144 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377197 | GTTTACTTTTAAAGG[A/G]GTCATCTGAGAATCC | 58513 |
rs748379106 | snp | G/T | 1.76924e-05 | 0.0029742 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437060 | ATCATAGGTGGGTGG[G/T]TTTGCTGAAAAGGAT | 58513 |
rs748392149 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439655 | GTGATCGCACCACTG[C/T]ACTCCAGCCTGGGCA | 58513 |
rs748413117 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425565 | TCAAGCCAGACTCCA[C/T]ATGCATCCCTTCACC | 58513 |
rs748437356 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415141 | CCAGGGTTTAGTGCC[C/G]TTATAAGAAGGACCC | 58513 |
rs748439641 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397307 | GTTGGGCAGGCCAGT[C/T]TTGATCTCCTGACCT | 58513 |
rs748456303 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443880 | TCAGTCTGGCCAACA[C/T]AGTGAAACCCCGTCT | 58513 |
rs748463326 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441775 | GGTCTGCAGCGACCA[C/G]GCCACTACCCAGGAG | 58513 |
rs748486793 | snp | G/T | 1.88064e-05 | 0.0030664 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386148 | AGGAATAGTCAGGAA[G/T]AAAAATAAGTCATGG | 58513 |
rs748488000 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386251 | ATGAAAGGAGAGAGG[A/G]AAGAGTAAAAAGCAG | 58513 |
rs748492495 | in-del | -/GAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428606 | AGAAAAGAAAAAAGA[-/GAG]AAAGAAAAAAGAGAG | 58513 |
rs748497898 | in-del | -/TAATAATAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393118 | TAATAATAATAATAA[-/TAATAATAAA]CAACGCAGGTAAATC | 58513 |
rs748546410 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391513 | AGAAGGAGGGTGAGT[C/G]CCCGTCTCTGAGCAG | 58513 |
rs748578544 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379481 | TCCCAGGGTTTCCCT[C/T]GAGAATCTGAATGCA | 58513 |
rs748593570 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404437 | TCAAGCCACAGGTGC[C/T]TGGACACTTTTCCAC | 58513 |
rs748628139 | snp | A/G | 1.70851e-05 | 0.00292271 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441880 | GAGAAATCACTATTC[A/G]TCTTCACATACCTTC | 58513 |
rs748629497 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434229 | CTGGACCCACAGGAG[C/T]GCTGATGAAAGCCCC | 58513 |
rs748632112 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390120 | AGCCCCAACACTATG[C/T]TACTTACAAAAGACA | 58513 |
rs748658702 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362904 | GGCTTCTGCCAAGCA[C/G]GGAACTCCAGGATGC | 58513 |
rs748682467 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433230 | CCTCCTGGGTTCAAA[C/T]GATTCTCCTGTCTCA | 58513 |
rs748699829 | snp | C/T | 2.89038e-05 | 0.00380146 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361755 | AGGGAGTGGGGTGGC[C/T]CGGAGGCGGAGGACT | 58513 |
rs748720061 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403511 | GAAGATGCTGTGTGC[C/T]CAGGAAAGGAAAGTG | 58513 |
rs748737780 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472899 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 58513 |
rs748744240 | snp | G/T | 1.69189e-05 | 0.00290846 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425218 | GGGGACGGCGCCAGG[G/T]AACACAGTCTTCTTT | 58513 |
rs748768575 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359529 | GATCATTTCCTCTGG[A/G]AAAAAACTGGGGTAT | 58513 |
rs748796629 | snp | C/G | 1.65864e-05 | 0.00287974 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441910 | CCCAAGGATAATGTC[C/G]GAGAGGCCAGACTTC | 58513 |
rs748803125 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366810 | TCACTGTAGGGCCAC[C/G]GCCCTCAGCCCAAAC | 58513 |
rs748808012 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465394 | TTTGGATTCTCCTAA[A/G]GACAACTGGCTGGGA | 58513 |
rs748846686 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371039 | TTATCTCTCTGAGAT[A/C]ATCGTGGGAACGAAA | 58513 |
rs748854857 | snp | C/T | 3.31318e-05 | 0.00406999 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404565 | GTGCATAGGGCGCTG[C/T]CCCGGAGGTGGCCGG | 58513 |
rs748864887 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404911 | CCACGGCCAATGTGT[A/G]CCTCTTGGGCTGGAG | 58513 |
rs748896208 | snp | A/G | 0.000231957 | 0.0107668 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442187 | ACTTACCTGCTTGTA[A/G]TAAGATTCATACAAC | 58513 |
rs748903599 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411125 | GCAAACAGGTGTTCG[C/T]ACGAAAACCTGCAGA | 58513 |
rs748905023 | snp | C/T | 3.36491e-05 | 0.00410163 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442241 | ATGAAACCACAGATA[C/T]TGGTCAAAAGTGAAC | 58513 |
rs748944338 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369654 | GCCAGGCAAGGGCTG[A/C]ACCAGCCCTGGAAGA | 58513 |
rs748945762 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379996 | GCTTCCAGTCACACC[A/G]ATGCAGCTGTCTAAA | 58513 |
rs748949186 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454323 | GGGCAATCTAGCAGG[C/T]GCAGTGTGTGACCTG | 58513 |
rs748949755 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409494 | AAGGATAAACCAGAC[A/T]TCACCAACATTAACA | 58513 |
rs749032917 | snp | A/T | 1.65053e-05 | 0.0028727 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436977 | GAGGGCGGTGTGACC[A/T]TCAGAGGGCTGCTGG | 58513 |
rs749055249 | snp | A/G | 6.59446e-05 | 0.00574177 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395470 | TGAAAGGATCATCCT[A/G]CAATTTTGTGAAGAA | 58513 |
rs749084796 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419203 | AATGGCTCATGCCTG[C/T]GTTCTCAACACTTTG | 58513 |
rs749124401 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461305 | AAGACTCCGTCTCTT[-/A]AAAAAAAAAAAAAAA | 58513 |
rs749135227 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460697 | CCAGCACGGGGGTGC[C/T]GCGGGCACAGAGCGT | 58513 |
rs749139966 | snp | A/C | 1.64939e-05 | 0.0028717 | synonymous-codon, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377171 | CTTCGGAGGCAGAGC[A/C]GGAGTGTCCTGTTTA | 58513 |
rs749189521 | snp | C/T | 3.47222e-05 | 0.00416652 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437053 | GAATTAAATCATAGG[C/T]GGGTGGGTTTGCTGA | 58513 |
rs749211930 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386837 | TTCTGCCATCTGCTG[C/G]TGAGTGTCTGCAGTG | 58513 |
rs749220960 | snp | C/T | 1.65531e-05 | 0.00287686 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418076 | GGTCTTTGCTTAACT[C/T]CCCCGTTTGCCTCGT | 58513 |
rs749221664 | snp | G/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472182 | CTTCCGTGCTCTCTT[G/T]CCCGTTCCCCTACTC | 58513 |
rs749231663 | snp | A/G | 1.65326e-05 | 0.00287507 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377280 | GGACATGAAAGAGAG[A/G]CAAAAATAGTTGTTA | 58513 |
rs749246176 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429645 | CCACAGGAACTGCTC[C/T]AGAACACACACCTGA | 58513 |
rs749259429 | snp | A/G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460142 | GAAAATTAGCTGGGC[A/G/T]TGGTGGTGTGCTGAG | 58513 |
rs749331843 | snp | A/G | 0.000389345 | 0.0139471 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361745 | TGCAAGCGGAAGGGA[A/G]TGGGGTGGCCCGGAG | 58513 |
rs749373763 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467569 | GGCCAGTGCAGGTCA[A/G]TAAGTGACAGTCAGG | 58513 |
rs749374719 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432058 | ATTTCGGTGTATGAT[-/A]GGGGCCCTGGAACCA | 58513 |
rs749388034 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355962 | TGCCCACCGCCCAGC[A/G]GAGGGTCCGATGTGC | 58513 |
rs749423339 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365203 | GAAGACGGTGTGGGG[A/C]ATGGCGGCCACCCCC | 58513 |
rs749434959 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438058 | AATGAATACACTAAA[A/G]TGGACTTATCCTGGC | 58513 |
rs749441247 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366922 | ACTTCTGCTAACTCC[C/T]TAATCGTTTTTTCCG | 58513 |
rs749462507 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396148 | TGAAGAAGTATGAAC[C/T]TGAGTGAATAATAAT | 58513 |
rs749503296 | snp | A/T | 1.69235e-05 | 0.00290886 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404786 | TTACGTGAGGATGGG[A/T]AAAATGAAGCATGTC | 58513 |
rs749541309 | snp | G/T | 1.64825e-05 | 0.00287071 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395309 | ACATAAAACACACAG[G/T]CTTTCAATGAGAAAG | 58513 |
rs749562369 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394165 | ACCTGCCCTCAAAAC[C/G]TTGGCAAATCAAAGA | 58513 |
rs749586023 | snp | G/T | | | missense, nc-transcript-variant, utr-variant-3-prime, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355736 | TCAGCCTTGCTGAGC[G/T]CGATGGCCAGTTCCA | 58513 |
rs749587009 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406687 | TTTGGCCTGCCCAGA[A/G]AAGTTCCCTCCTTTA | 58513 |
rs749591266 | snp | C/T | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413773 | GAACGAGACCCTTAC[C/T]TGCACCTCGCTGGTT | 58513 |
rs749603492 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391177 | TTAAGATGTTAGAAG[A/G]GCAAAGTAACCCCAA | 58513 |
rs749641020 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433059 | CAAGTAATCTGCCCG[C/T]CCCAGCCTCCCAAAG | 58513 |
rs749642077 | in-del | -/CAAATACC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417471 | GCAAACTTCCAGGTG[-/CAAATACC]AGCCTCTGATATTTC | 58513 |
rs749646475 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403282 | AGGCAGCTTAGAGAA[C/T]GGGGGTCCTGCATGG | 58513 |
rs749671176 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361653 | AAATAACGCGAGGGA[C/T]AGAGAGTGTGAGGTA | 58513 |
rs749673235 | snp | C/T | 3.30355e-05 | 0.00406407 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403717 | CATGTGGCAGGGACC[C/T]GACTCCGTGAAGTAC | 58513 |
rs749738961 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415589 | GCCCTTGCTGGCTTA[C/T]GGCAGTGTGAAATCA | 58513 |
rs749748208 | in-del | -/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430524 | GCTGCAAGTGCTGGA[-/TG]TGTGTCTTCACGCAG | 58513 |
rs749794018 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360774 | AATTGACAAATAAGC[C/T]ATAGGATAGCTGTGC | 58513 |
rs749799345 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374324 | TTTCTGCAGAGCACC[A/G]AGTGGCACAGCAACC | 58513 |
rs749812015 | snp | G/T | 1.64879e-05 | 0.00287118 | splice-acceptor-variant | EPS15L1 | GRCh38.p7 | 19:16440911 | GCCAAGTCCCATATC[G/T]GCGGAAACACAAAAA | 58513 |
rs749825237 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445276 | AAGGCTCATCCGGCT[C/T]GAACACTTGATGACC | 58513 |
rs749829046 | snp | A/C | 1.67835e-05 | 0.0028968 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421524 | GAAGCTTTTTATGAC[A/C]CCCAGACACATGCTT | 58513 |
rs749833602 | snp | A/C | 3.83112e-05 | 0.00437655 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386131 | AGCTCTGCTACTGCC[A/C]AAGGAATAGTCAGGA | 58513 |
rs749899306 | in-del | -/ATAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433963 | GCAAGACTCCATCTC[-/ATAA]ATAAATAAATAAATA | 58513 |
rs749904978 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380432 | GGCTTCTAGCGTTTA[C/T]TCATACCAATGCAGC | 58513 |
rs749909323 | snp | A/C | 3.35999e-05 | 0.00409864 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437037 | CTTTGTGGCTGGCAC[A/C]GAATTAAATCATAGG | 58513 |
rs749917980 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465710 | AAGACAATAAGCAGG[A/C]CTTTCCATGTCCCTC | 58513 |
rs749980216 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436176 | GGGAGCAAACCAACC[G/T]TGTAAACATGGGACG | 58513 |
rs750019015 | snp | G/T | 1.65121e-05 | 0.00287329 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437742 | CTGGTATTAGAAGAA[G/T]GTGAACTTGAAGGAC | 58513 |
rs750057084 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363565 | TCCTTGTGGGCTCCG[A/G]GGCTACAGCCCCCAT | 58513 |
rs750112735 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417498 | TTTCCGATAACAACC[C/T]GGGAGAGTTCGTGTA | 58513 |
rs750118617 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360136 | GGAAATAGAATTATG[A/T]ATTTCAGAAAGAGAA | 58513 |
rs750164423 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448140 | AAAACATAATCCTCA[A/G]GATCTAGGGCAAAGC | 58513 |
rs750168461 | snp | C/T | 1.68238e-05 | 0.00290028 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421310 | CAACTGCCACCTGTC[C/T]GGCCTTACCATATGT | 58513 |
rs750177612 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473929 | ACGCCACTGCACTCC[A/G]GTTTGGGCAACAAGA | 58513 |
rs750179589 | snp | C/T | 8.24844e-05 | 0.00642148 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392280 | GGCACGCAGCTCTCC[C/T]GGGCAACGTCCCACC | 58513 |
rs750191435 | snp | A/G | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395353 | AGATACCTTTGAAGG[A/G]GTCAGCTCCTTTAAA | 58513 |
rs750210600 | snp | A/C | 1.64904e-05 | 0.00287139 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413765 | ACCAAAACGAACGAG[A/C]CCCTTACCTGCACCT | 58513 |
rs750225620 | in-del | -/AC | 4.94462e-05 | 0.00497199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395300 | TAAATTCGACATAAA[-/AC]ACACACAGTCTTTCA | 58513 |
rs750228302 | snp | A/G | 3.6517e-05 | 0.00427284 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361731 | AATCCCAGGGAAGCT[A/G]CAAGCGGAAGGGAGT | 58513 |
rs750234742 | in-del | -/CACAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392505 | CCAGACATAAAAGAA[-/CACAT]CACAGAATGATGCCG | 58513 |
rs750262553 | snp | C/G/T | 9.702e-05 | 0.00696433 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425277 | GCAGGGCGGAGGGCA[C/G/T]GGGCTCCTTCTCCAG | 58513 |
rs750305456 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371900 | GGGAGGTGTGTGCCA[C/T]GGCTAACTTTAACCT | 58513 |
rs750308808 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456187 | CCTGGGCAACAAGAG[A/G]AAAACCCTGTCTCAA | 58513 |
rs750315979 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411828 | CCTCAGCCTCCTGAG[C/T]AACTGGGACTACAGA | 58513 |
rs750324346 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443128 | GCACACAAACCTGCC[A/G]CTGATGTAATAAGCG | 58513 |
rs750336545 | in-del | -/AC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400371 | CAAAAAAAAAAAAAA[-/AC]CCCTGACTTTTGAGA | 58513 |
rs750358393 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381369 | CTGCCCTCAGCTGCC[A/G]AGGGCCACCCCAGTG | 58513 |
rs750364259 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455258 | GAGTAATTGGGACCA[C/T]AGCCATGCACCACCA | 58513 |
rs750367780 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395446 | TGCTAAATAACAAGG[C/T]TTTATTTTTGAAAGG | 58513 |
rs750418112 | snp | A/G | 1.73342e-05 | 0.00294394 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413875 | ATATTTCATGAAAAC[A/G]AGAGTGAATAATAAG | 58513 |
rs750421709 | in-del | -/G | 1.84701e-05 | 0.00303887 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361999 | CTGGAAAGTTTAGGA[-/G]GAAAAAAAAAAGGAG | 58513 |
rs750480530 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366775 | TGACCAGACGCTTTG[A/G]GCAAAGAAAGCCCCC | 58513 |
rs750508122 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372609 | TCCCAGAATGTGTGC[A/G]GCCACCTCAGCTGCC | 58513 |
rs750536632 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464903 | GCCTAACCAGTGAAA[-/C]CCCGTCTCTACTAAA | 58513 |
rs750537248 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403752 | TTGATTTCGTCTTGC[A/G]TTGACTTCAGGGACT | 58513 |
rs750565169 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419772 | GTTATCCCCACAGTT[C/G]GAGGCCCTGACGATT | 58513 |
rs750566308 | snp | C/T | | | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403913 | CTGAGATTGGATTTG[C/T]GTTTTCAGTGATGAG | 58513 |
rs750605355 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432111 | ACAACTGTACTTTTA[C/G]TTAACAGAAACAAAT | 58513 |
rs750608389 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401529 | AACATCCAGACATGC[A/G]CGGCCCGGCCCATCC | 58513 |
rs750617704 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462095 | GCTTTGGAGCCCATG[A/G]TCTGATTCAGACGCC | 58513 |
rs750639855 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387741 | ACTGCACTCCAGCCT[A/G]GGCGAAAGAGCGAGA | 58513 |
rs750680940 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430721 | CTGACCAGATGCACG[A/G]TGTGTGAGTGCCTGG | 58513 |
rs750694121 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386751 | CTCAGGCTGGCCTCT[C/G]CACACGCAAGCCTGG | 58513 |
rs750709081 | snp | A/G | 7.36296e-05 | 0.00606707 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386225 | CACTGGATTCAAAGG[A/G]GTCGAGCTAAATGAA | 58513 |
rs750713818 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358041 | GTGGGTGGGAGCTGA[C/G]AGTAATGTTCGCCTG | 58513 |
rs750730688 | snp | A/G | 5.24379e-05 | 0.00512018 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441852 | GGGGGGAGCTGTGAG[A/G]GCAGCCACAGAAGAG | 58513 |
rs750745232 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374022 | ATCTGCAGTTGCTCC[A/G]GACTTAAAATGCTGC | 58513 |
rs750751808 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383604 | AAGGAGGGGGGCGCC[A/G]TGCCAGGGCCTCTGG | 58513 |
rs750765005 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382266 | GCCCGCGTCATTTCC[A/G]AATCCCAATTTTCAT | 58513 |
rs750784634 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404704 | GTTTCTGAGCCTCGA[A/G]CTCCTGCAAACTGCT | 58513 |
rs750806123 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457328 | CTGCCAAGAGCTAGA[C/T]GGAAGAGACAGGATG | 58513 |
rs750806241 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393919 | GGACTGGACACAGTC[C/T]AAAGACCGGTCCGGG | 58513 |
rs750820714 | snp | C/T | 3.35993e-05 | 0.0040986 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361958 | GAAAGTCTGCGGAAC[C/T]AAGCTGGCTTACAGG | 58513 |
rs750850162 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355683 | CCGCCCGTGCCCTGT[C/T]CCGCCTACACACGGC | 58513 |
rs750861158 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468844 | TAGCAAGACTTCATC[C/T]CTTCAAAAAAAAAAT | 58513 |
rs750877169 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367936 | TGGTCTCAATCAATC[C/T]GATTAATAAAAATAT | 58513 |
rs750910688 | snp | G/T | 7.7818e-05 | 0.00623722 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362031 | AAGAAAGAAATATGA[G/T]TTACTCACCCGGACA | 58513 |
rs750917597 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434453 | TTGATGGGCAAGAGG[C/T]TTTCAAAAATCCCAT | 58513 |
rs750961450 | in-del | -/TCTC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470690 | GGCTAGCTGTGCACT[-/TCTC]TCTCCTTGGATCAGC | 58513 |
rs751011999 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433551 | TAGAAAAGAGCCAGG[A/C]GTGGTGGTGCTCTTG | 58513 |
rs751017829 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407783 | CTTCAGGGCAGTCTC[C/T]GTCTTCCCCCTTCAT | 58513 |
rs751064173 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391224 | AAATGGAAAAAAATA[C/G]AAATAGAAAAGAGAA | 58513 |
rs751066118 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356134 | CCCGCCCCACGCAGA[A/G]AAGTGAGGATGGGCC | 58513 |
rs751080665 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448056 | TCCATAGGAAAAACA[C/T]GGGCCTCGAACTAAA | 58513 |
rs751104406 | in-del | -/GGGAGTGG | 3.38404e-05 | 0.00411328 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361741 | AAGCTGCAAGCGGAA[-/GGGAGTGG]GGTGGCCCGGAGGCG | 58513 |
rs751122999 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446903 | CCCCATAATGGCTAT[A/G]TTTTTCAATGCCACT | 58513 |
rs751127564 | in-del | -/AGTG/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367985 | GAGAGAGAGAGAGAG[-/AGTG/GT]TGTGTGTGTGTGTGT | 58513 |
rs751130231 | snp | A/C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362668 | GCATGAGCCACCATG[A/C/T]GTGGCTAATTTTTGT | 58513 |
rs751159765 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416404 | ACTTTGGGAGGCCAA[A/G]GCCAGAGGATCACTT | 58513 |
rs751223293 | snp | A/G | 4.96266e-05 | 0.00498105 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377140 | TGGGCGGTTTAGGCC[A/G]TGGAGGAGCAGGTTT | 58513 |
rs751231215 | in-del | -/ATAATAATAATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393081 | CAGGAGCTGGATATA[-/ATAATAATAATA]ATAATAATAATAATA | 58513 |
rs751247538 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440857 | CTGTGTACATGTGTA[C/T]ATACCTGTTTGTCCA | 58513 |
rs751265283 | snp | G/T | 1.7822e-05 | 0.00298507 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402280 | GCTGTCACACCAGGG[G/T]ACCAGAGCCCCATAC | 58513 |
rs751265589 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415315 | TCTGATGTTTCAGTC[A/C]CCCATTCAGAGTGGT | 58513 |
rs751274323 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370365 | CCAGAGCCCCCTTCT[A/G]AGGCGTCTGCCCCAG | 58513 |
rs751287450 | in-del | -/ATAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433966 | GACTCCATCTCATAA[-/ATAA]ATAAATAAATAAATA | 58513 |
rs751288595 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455172 | GTCCAGGCTGGAGTG[A/C]AGTGGCACGACCATA | 58513 |
rs751298085 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358111 | GCTGGGTCTGAACCA[C/T]AGCCCTCTGGCCGCC | 58513 |
rs751333173 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371346 | GCCACACACAGGTAC[A/G]GGAGGGGCTTGTTTG | 58513 |
rs751333503 | snp | C/T | 1.66302e-05 | 0.00288355 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425080 | CCGCTGAGGGCTCCG[C/T]ACCTGTGTTTGCTTG | 58513 |
rs751371626 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417270 | CACAGGCTCTGCCCA[C/T]GACCTGCCTGGGACC | 58513 |
rs751378889 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441487 | AAAAAAAATTAGCCG[G/T]GTGTGGTAGCATGTG | 58513 |
rs751391250 | snp | C/T | 4.95552e-05 | 0.00497747 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385246 | AGTCAGAGTTACAGG[C/T]CTTTAAGAGAACATG | 58513 |
rs751407853 | snp | A/G | 1.79364e-05 | 0.00299464 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386194 | TTTGAGGAGACACTG[A/G]AGGATGAAAAGGGAT | 58513 |
rs751408213 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374019 | CAGATCTGCAGTTGC[G/T]CCGGACTTAAAATGC | 58513 |
rs751425244 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369217 | GGCACCAGCCCCGCG[C/T]GCACTCTGCCTTAGA | 58513 |
rs751441073 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422019 | GTGTGAGTACACACA[C/T]GTCACTGACAGGTAA | 58513 |
rs751476172 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453979 | TGTGACAAATGAGGA[C/G]AGCTTGGTGACAGGA | 58513 |
rs751485911 | in-del | -/AAAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387899 | AAAAGAATGAAAAAT[-/AAAT]AAATAAATAAATAGA | 58513 |
rs751492265 | snp | A/G | 7.00329e-05 | 0.00591706 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441842 | CCTGACCTGCGGGGG[A/G]AGCTGTGAGGGCAGC | 58513 |
rs751495521 | snp | A/G | 0.000162668 | 0.00901706 | synonymous-codon, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16355830 | GCTTGGCCCACGCCA[A/G]CTGCTGCTCCTCATT | 58513 |
rs751509791 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379801 | TCTAAGGCTCCAGTA[C/T]CTAGTCACACAGATG | 58513 |
rs751511828 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392235 | AGGGAAGGGGGCCTT[C/T]GGGAAGCGCCACCCT | 58513 |
rs751536858 | snp | A/G | 6.69748e-05 | 0.00578644 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404767 | AGGGAGGAGTTGCAG[A/G]GGTTTACGTGAGGAT | 58513 |
rs751565778 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421206 | AGGACGCCAGACACA[A/G]CGGAAGCCTGTGACA | 58513 |
rs751572012 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434422 | TGGCTTGACTTTGTC[C/T]CCAGAGAGCAAACCA | 58513 |
rs751582706 | snp | A/G | 1.67164e-05 | 0.00289101 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425188 | GTCTTTTGGTGGGGG[A/G]CTGGCAGGCAGGACG | 58513 |
rs751583114 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435072 | CCTCAGCACTCGTAC[A/C]TCCCGAGTAGCTGGG | 58513 |
rs751587680 | snp | A/G | 1.6757e-05 | 0.00289452 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361941 | TGGATCGGGGGCCTC[A/G]GGAAAGTCTGCGGAA | 58513 |
rs751672630 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386429 | ACCTATCAACCTGGA[C/T]GGAATATCCCCAAAA | 58513 |
rs751672991 | snp | A/G | 0.000219496 | 0.0104738 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362019 | AAAAAAAGGAGAAAG[A/G]AAGAAATATGAGTTA | 58513 |
rs751712273 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358892 | AAAAGAACCGTTCCG[C/T]TAACCTAGAAATGCC | 58513 |
rs751716828 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468234 | TGATGTTCTAGCAAC[C/T]GGAGCAACACAGCTA | 58513 |
rs751765806 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429253 | ACAGGTGTCAGGCCA[C/G]TCAGTGCGCTGAAGA | 58513 |
rs751778549 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401074 | TCGTAACTCATGAAG[A/G]ATGAATGCTCATCGT | 58513 |
rs751781533 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399609 | AATTCCTGTGGTGTA[A/C]ACAGTCTCATCATGG | 58513 |
rs751829515 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411701 | CACCACCCCATATTA[C/T]TTATTCATTTATTTT | 58513 |
rs751848700 | snp | A/G | 1.66194e-05 | 0.00288261 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403693 | CTCTTGGGGCTCGCT[A/G]GTCCCTGGCATGTGG | 58513 |
rs751857028 | in-del | -/GAAAAGAAAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428546 | AAAGGAAGAAAGACA[-/GAAAAGAAAG]GAAAAGAAAGGAAAA | 58513 |
rs751870529 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381626 | CCAAGTACGAAGCTG[C/T]GATTGGAATCTGGGA | 58513 |
rs751874658 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396598 | TAAATCTAAAAACTA[C/T]TCTAAAATAAAAGTT | 58513 |
rs751896412 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443029 | GGGGAGTGTGCCAAC[C/G]TGGTGGGGAATTATG | 58513 |
rs751910737 | snp | A/C | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355076 | GAATTGTGTGAGTCA[A/C]GGAGTTTGAGACCAG | 58513 |
rs751916459 | snp | C/T | 1.65949e-05 | 0.00288048 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404560 | TGCCTGTGCATAGGG[C/T]GCTGCCCCGGAGGTG | 58513 |
rs751930330 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437636 | ATTAATTTTCTATTA[C/T]GTGAATTTCACCACA | 58513 |
rs751969566 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467028 | ATGAGAAAACTAAGG[A/T]ACAGAAAGTATTTGC | 58513 |
rs751986675 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377992 | GCTTAAAGAGAGAGA[C/T]AGTCAGAGATAGTTA | 58513 |
rs751989776 | snp | A/G | 4.9436e-05 | 0.00497148 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392382 | TTTCTTGAAGAAGTC[A/G]TCAGTGGCAGAGCCA | 58513 |
rs752000990 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406488 | GAGGTAGCCCAATGC[C/T]CCGAGCGATGCTCCC | 58513 |
rs752006693 | snp | C/T | 3.29663e-05 | 0.00405981 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404616 | TCCTGGCACTTCTGC[C/T]GGACGTCGCTCAGCA | 58513 |
rs752028674 | snp | C/T | 9.9827e-05 | 0.00706424 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442210 | CATACAACGAATTTC[C/T]AGTGGGAATCTGTAA | 58513 |
rs752033040 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360463 | CAGGGTCTTGGGCGA[C/T]TTAAATAAGCCACAT | 58513 |
rs752035127 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366760 | TCTCGACCTTGCTAA[C/T]GACCAGACGCTTTGA | 58513 |
rs752066506 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452527 | CGAGAAGCTAAGGCA[A/G]GAGGATTGCCTGAGG | 58513 |
rs752078366 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361085 | AATCTGGAATATTTT[C/T]TCACACAGAGAAAAA | 58513 |
rs752116529 | snp | C/T | 6.86224e-05 | 0.00585717 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16471993 | GAACGGGGGCGGGGC[C/T]GCAGCCACGCGTGCG | 58513 |
rs752118427 | snp | A/C | 2.04899e-05 | 0.00320071 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428710 | GACTTACCACAGCGA[A/C]CTCATCTCGATCCAA | 58513 |
rs752119114 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358301 | GTGAGGTCTGTATGC[A/G]CTTAGGAGGCACGCT | 58513 |
rs752143001 | snp | C/G | 1.6649e-05 | 0.00288518 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425075 | TGTGCCCGCTGAGGG[C/G]TCCGTACCTGTGTTT | 58513 |
rs752150791 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405677 | TGCCTTACAGTGGGA[A/C]ATGAGCACACTGCAT | 58513 |
rs752161746 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393901 | CATGCGACTTCTGAG[C/T]CAGGACTGGACACAG | 58513 |
rs752166419 | snp | C/T | 0.000163252 | 0.00903323 | missense, nc-transcript-variant, utr-variant-3-prime, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355755 | TGGCCAGTTCCAGGT[C/T]CTCCTGCTCCTGCCG | 58513 |
rs752189537 | snp | C/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404635 | CGTCGCTCAGCATGT[C/G]TCGGAGCTTGGCCTT | 58513 |
rs752201350 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388965 | CTTCAAGAATGACAA[C/T]AGGCCTGGCACAGTG | 58513 |
rs752230566 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458518 | CTCACCCACGGCCCT[A/G]CCTTCACCCGCTTCC | 58513 |
rs752234863 | snp | C/G | 3.2969e-05 | 0.00405998 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404715 | TCGAGCTCCTGCAAA[C/G]TGCTTGTTTCCCGGT | 58513 |
rs752235753 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426061 | TTGACCGTATCAAGG[C/T]GTGCCCCACATGAGA | 58513 |
rs752286367 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455591 | TCCCATCTTGCTTCA[C/T]TAAGAGAAGCTGTCT | 58513 |
rs752288809 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415196 | GCCCTGTGAGGACAC[C/G]GCAAGAAGGTGACTC | 58513 |
rs752391253 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379723 | ACCATCTAAGGCTCC[A/G]GCGTCTAGTCACACA | 58513 |
rs752396334 | snp | A/G | 1.65389e-05 | 0.00287562 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413745 | TTTAGCACAAAGTAG[A/G]TGTAACCAAAACGAA | 58513 |
rs752415427 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468732 | AGAAGATGAATCCTA[C/G]CCAGATGCAGTGGCT | 58513 |
rs752421772 | snp | A/C | 0.000325212 | 0.0127476 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417929 | TCAATACCCCCAGGG[A/C]ATGACCAGCACCACT | 58513 |
rs752443591 | in-del | -/AG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427273 | TGGGGTGACAGAACA[-/AG]ACTCTGTCTCAAAAA | 58513 |
rs752444734 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390830 | AAGTATTCAAATATA[C/T]GAAATACATGTAAAG | 58513 |
rs752447796 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368296 | TACACAACAGTGGAC[A/G]CACACATACAACCAT | 58513 |
rs752461112 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424483 | CCAGTAAAGTACCTC[C/T]CCTAACCTGACTTTC | 58513 |
rs752510753 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420943 | GCCAGGCCACTCTGC[C/T]AGAGGCTCCAAGGCC | 58513 |
rs752544779 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464876 | ATCACAAGGTCAGAT[C/T]GAGACCATCCTGCCT | 58513 |
rs752557108 | snp | C/T | 1.65575e-05 | 0.00287724 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440766 | TCATGCCTAGTAATA[C/T]TTGACAGTGGAGGAA | 58513 |
rs752629997 | snp | A/G | 3.30256e-05 | 0.00406346 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385236 | GCACCAACAAAGTCA[A/G]AGTTACAGGTCTTTA | 58513 |
rs752655086 | snp | C/T | 3.45393e-05 | 0.00415554 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425305 | CAGGGCTCGGTACAC[C/T]AAGTGCATGGCCTGC | 58513 |
rs752671351 | in-del | -/TGGA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378116 | TGAATGGCGGGTGGG[-/TGGA]TGGATGGATGGATGG | 58513 |
rs752672014 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389245 | GGATTGCTTGAGCCT[A/C]GGAGTTTGAGACCAG | 58513 |
rs752688541 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432535 | ATTGCGCCACTGTAC[C/T]CCAGCCTGGGCAACA | 58513 |
rs752694892 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421453 | CATCTTGTCTGCCAC[A/G]GGCACCACCCAGTTC | 58513 |
rs752707354 | snp | C/T | 1.66026e-05 | 0.00288115 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442202 | ATAAGATTCATACAA[C/T]GAATTTCCAGTGGGA | 58513 |
rs752708341 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392371 | TTCTTTGTCTGTTTC[C/T]TGAAGAAGTCGTCAG | 58513 |
rs752736035 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403148 | TGTGTAGACTGGATG[C/T]CCAGGGCCAGGACAG | 58513 |
rs752749690 | snp | A/G | 1.64887e-05 | 0.00287125 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440848 | CCATTTGCTCTGTGT[A/G]CATGTGTATATACCT | 58513 |
rs752754414 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421115 | CTGAAAGACAGTGAA[A/C]TGACCGTCACGGAGC | 58513 |
rs752754794 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393183 | GGTGCCAGGGGTTGC[A/G]GGAGGGAATGGGGAG | 58513 |
rs752770578 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472541 | CTACTCAGGAGACTG[A/G]GGCAGGAGAATTGCT | 58513 |
rs752782676 | snp | A/G | 1.69622e-05 | 0.00291219 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361864 | TCTTTTCCACTAAAC[A/G]GGTCCCCAAACCCCT | 58513 |
rs752789843 | in-del | -/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374872 | ACACACGCACGCATA[-/TG]TGTGTGCACGTTTGC | 58513 |
rs752795458 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442900 | GGTCACGCAGCTAAT[C/T]GGGGCCACCAGAGGC | 58513 |
rs752796557 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427085 | GGCGAGAGAGTGATG[C/G]AGGGAGGGAGGAAGA | 58513 |
rs752845120 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398422 | GACGTCAGGTGCTGA[C/T]GACCACAAGACACAC | 58513 |
rs752845731 | snp | A/G | 2.05603e-05 | 0.0032062 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428705 | AGCAGGACTTACCAC[A/G]GCGAACTCATCTCGA | 58513 |
rs752872450 | snp | A/T | 3.34739e-05 | 0.00409095 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361926 | CCCGAGTGGCTGGAA[A/T]GGATCGGGGGCCTCG | 58513 |
rs752888514 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413257 | GGTGACAGGCCACTG[-/C]CAACTCTGTGCTGGT | 58513 |
rs752900292 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409022 | AGGCCAGGTGTTTGA[C/G]ATGAGCCTGAGCAAT | 58513 |
rs752916762 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469000 | ACTCCAGCCTGGGGG[-/A]CAGAGCGAGACCCTG | 58513 |
rs752920405 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441300 | ACACAGTGAAACCCC[A/G]TCCCTACTAAAAATA | 58513 |
rs752941213 | in-del | -/AAATTTGTAAAAATACAAATT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408462 | AACCCAGTAAAATAC[-/AAATTTGTAAAAATACAAATT]TTTACAAAATTTTGT | 58513 |
rs752956381 | in-del | -/T | 1.67091e-05 | 0.00289038 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421514 | AGTTAATCTGGAAGC[-/T]TTTTATGACCCCCAG | 58513 |
rs753002798 | snp | A/G | 6.62021e-05 | 0.00575297 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417620 | AAACTCCCCGGAGCC[A/G]AGAGAGCCTGAACTG | 58513 |
rs753037814 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364954 | CCAGACTGCTTGAGG[A/G]CTTCTCCCGCTTGGG | 58513 |
rs753086594 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449302 | AAGAAGAAAAGAACA[C/T]GGGCAAAAGATCTGA | 58513 |
rs753087349 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405642 | TCCTTGGCCATGGAA[C/T]GGGATGGCGCCGTGT | 58513 |
rs753108852 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448236 | ATGTTTGCACTGTGA[A/C]AGAGCCATGTAAGGC | 58513 |
rs753135786 | snp | G/T | 3.3e-05 | 0.00406189 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403880 | CAGATCGTCTTCCTG[G/T]GACTTTAAGTCAGAT | 58513 |
rs753143030 | snp | A/G | 1.69132e-05 | 0.00290797 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421303 | ACAGCCACAACTGCC[A/G]CCTGTCCGGCCTTAC | 58513 |
rs753167778 | in-del | -/ACTAACACTAAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464767 | AACACTAACACTAAC[-/ACTAACACTAAT]ACTAATGATAGCTGA | 58513 |
rs753209084 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429001 | ATTGATTATAAGATT[A/G]TAAGTTTAAAGGCTA | 58513 |
rs753216282 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473469 | GCTGAGAACTCACCA[C/T]TGCACTCCAACCTAG | 58513 |
rs753275318 | snp | A/G | 3.7482e-05 | 0.00432892 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437905 | AGTAAACAGCATATC[A/G]CCAGTGAGGGTAGGG | 58513 |
rs753298624 | snp | A/G | 1.65023e-05 | 0.00287244 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385220 | AAGGGATCTGCAATC[A/G]GCACCAACAAAGTCA | 58513 |
rs753305090 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381528 | GCTCCGGCAAGAAGG[A/C]AATGAGGTGCCATGT | 58513 |
rs753313759 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416947 | AAACTAAGGCACTAG[A/G]CAAGAAGGGGAGCCA | 58513 |
rs753315116 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421435 | GAATATCTCATCAAA[C/T]CGCATCTTGTCTGCC | 58513 |
rs753325589 | snp | A/T | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354920 | AATTGTCTAAGGGGC[A/T]TATGGGAACTCTTTG | 58513 |
rs753344863 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432865 | TGGAGTGCCATGGCA[C/T]GATCTCAGCTTATTG | 58513 |
rs753345025 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407586 | CAGACTCAGTCTCCC[A/G]AAGTGCTGGGATTAT | 58513 |
rs753364035 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437468 | ATAAAATTAGTGGTT[C/G]CCAGCGACTGGGAGG | 58513 |
rs753390827 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466720 | CCAGCCTAGGCAACA[C/T]AGTGAAACTCCATCT | 58513 |
rs753432890 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430956 | AGATGTATGCATGGC[C/T]GGGCACAGTGGCTCA | 58513 |
rs753469728 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423079 | AACAATGGTTAAACT[C/T]GTTTACTCTTCATGA | 58513 |
rs753476665 | snp | A/G | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404621 | GCACTTCTGCCGGAC[A/G]TCGCTCAGCATGTCT | 58513 |
rs753480358 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394552 | TAGAGAGCCTTCCTC[C/G]TGGAAATACTGTTTT | 58513 |
rs753484194 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361309 | CGATCTGCCTGAAGT[C/T]CTTCAATTTGCACTT | 58513 |
rs753528461 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380583 | CTCCAGGGTCTAGTC[A/G]CACAGACGCAGCCAT | 58513 |
rs753535276 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392562 | TAAGAACGCTAGTGA[C/T]GGAAAACAGGATAAT | 58513 |
rs753535402 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406328 | CTTATGGACATGTTC[A/G]ACAGGAAACTCAGGA | 58513 |
rs753540620 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465843 | AAACTTAAAAACAAA[A/C]AAACAAAAAAATAAC | 58513 |
rs753543976 | snp | A/G | 5.11592e-05 | 0.00505737 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361857 | AAATGGGTCTTTTCC[A/G]CTAAACGGGTCCCCA | 58513 |
rs753575371 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403026 | CATGCTTGCGATCAA[C/T]TGTGGCCTATAAACT | 58513 |
rs753603960 | snp | A/G | 3.39305e-05 | 0.00411875 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402324 | TTCAACCTTTACCAT[A/G]GCTCCAAAACTGCCC | 58513 |
rs753625100 | snp | A/G | 1.77931e-05 | 0.00298266 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413886 | AAACAAGAGTGAATA[A/G]TAAGCCTCCACCCCT | 58513 |
rs753652197 | in-del | -/GAATA | 0.00101123 | 0.0224631 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413880 | CATGAAAACAAGAGT[-/GAATA]GAATAATAAGCCTCC | 58513 |
rs753668897 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462329 | CCAGGGCTGGGGTCC[C/T]GTTGCCACCTGTTCT | 58513 |
rs753750678 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361021 | AGAGAACAAGATTTT[C/T]ATGTATCAAGGAAGC | 58513 |
rs753781756 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457129 | AGCGACTCACAATGC[A/G]GACACCCGGAGAAGG | 58513 |
rs753788989 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373422 | GGCTTTTTTTGGTTT[A/G]TTTGTTTGTTTTAAG | 58513 |
rs753804038 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360326 | TAAAGCAGGTTTTGT[C/T]TCTGGCTTTTATTAA | 58513 |
rs753817851 | snp | G/T | 1.73093e-05 | 0.00294183 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441867 | GGCAGCCACAGAAGA[G/T]AAATCACTATTCATC | 58513 |
rs753829078 | snp | A/G | 1.65051e-05 | 0.00287267 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437753 | AGAATGTGAACTTGA[A/G]GGACTTGGACACTCA | 58513 |
rs753842730 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453585 | CAGCGTGGTGGCAGG[C/T]GCCTGCAGTCCCAGC | 58513 |
rs753847449 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369047 | ATAGGTTCTAAAATT[C/G]ATCACTGCTCGGGGA | 58513 |
rs753863380 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413587 | CATAGGGTTTTTATA[C/G]AAGAAAAATAAAGTG | 58513 |
rs753919062 | snp | C/T | 4.94792e-05 | 0.00497365 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392287 | AGCTCTCCCGGGCAA[C/T]GTCCCACCCCACTCA | 58513 |
rs753977338 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423117 | TCCTGTGATGTCCAA[A/G]TCTAACAGGCTCCTG | 58513 |
rs753979847 | snp | C/T | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421436 | AATATCTCATCAAAT[C/T]GCATCTTGTCTGCCA | 58513 |
rs753997562 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396615 | CTAAAATAAAAGTTC[A/G]TTAAAAAATCATTGA | 58513 |
rs754001572 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408812 | AGTGGCATGAGGAGA[A/G]GCAGATAGGTCAATG | 58513 |
rs754007911 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392359 | GTAAATGGGTCATTC[C/T]TTGTCTGTTTCTTGA | 58513 |
rs754030805 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378872 | TTAAGTCTGTAATAA[A/G]ATAGAAAATAACTAC | 58513 |
rs754039227 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452881 | GGCTCACTGCAAGCT[C/T]CGCCTCCCCGGTTCA | 58513 |
rs754041249 | snp | A/G | 4.08914e-05 | 0.00452151 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361782 | GACTCAACTTACAGA[A/G]GTGAAGTCTGCAAAG | 58513 |
rs754054840 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407830 | TCCGTCAGGCCACAG[C/T]GCAGCCAACCCCTGT | 58513 |
rs754095283 | snp | C/T | 1.68858e-05 | 0.00290561 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425211 | GCAGGACGGGGACGG[C/T]GCCAGGGAACACAGT | 58513 |
rs754101036 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382127 | ACCTCGGGCCAAGCC[A/G]GCTTGGCGCCTCCCA | 58513 |
rs754163257 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362866 | GGTGGCTCCAAGGGG[C/T]AGCGTTTATCTGGGC | 58513 |
rs754168097 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436942 | GTTCACTTACCCTCA[C/T]AGCCCAGTGGGCCTC | 58513 |
rs754170836 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375102 | GCATGCATGTGTGTA[C/T]TGACAAGAGAATATG | 58513 |
rs754183597 | snp | C/G | 2.5581e-05 | 0.00357629 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425283 | CGGAGGGCACGGGCT[C/G]CTTCTCCAGGGCTCG | 58513 |
rs754194688 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375856 | ATGGCCAGCCCAGGG[G/T]ACAGGAGGAGAGAGG | 58513 |
rs754222608 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416513 | CATGGTGGCATGCAC[C/G]TGTACTCTCAGCTTC | 58513 |
rs754223152 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395409 | GTCTGGAAAGGATCC[A/G]GATGCAACTCTTGCG | 58513 |
rs754230253 | snp | A/G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447117 | CAGCCCTCCCAGCAG[A/G/T]CCGGCCCACATTCTG | 58513 |
rs754239491 | snp | C/T | 1.66153e-05 | 0.00288225 | synonymous-codon, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377129 | TTACTGACCGCTGGG[C/T]GGTTTAGGCCGTGGA | 58513 |
rs754247838 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418011 | GACTTGAGGAGGGTC[A/G]ATGCCTTTACTGACC | 58513 |
rs754248569 | snp | A/G | 3.48232e-05 | 0.00417257 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377079 | GGTCCCCCGCCATCC[A/G]GCACCGGTAGGCGGT | 58513 |
rs754273611 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427036 | ACTTAACCCTAAAAT[A/G]GTTCACAGGAAAACT | 58513 |
rs754320916 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469133 | AGGAAATGGCCCATT[C/T]CAGAGTCCAGCAGGC | 58513 |
rs754340038 | snp | A/G | 0.000117093 | 0.00765068 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418095 | CGTTTGCCTCGTATC[A/G]GCCAGGGCCCTGGGA | 58513 |
rs754344370 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442256 | TTGGTCAAAAGTGAA[C/T]ACAACCCCTTGGGGA | 58513 |
rs754412772 | snp | A/C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426224 | CCATGTGGGGCGGGT[A/C/G]TGACCTCCGTGGGAT | 58513 |
rs754431113 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444998 | TGCTGGGATTACAGG[C/T]ATGAGCCACCACGCC | 58513 |
rs754503381 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401292 | CTTCCCCATAAATCC[C/T]TGGGACTGAGGACTT | 58513 |
rs754527722 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421441 | CTCATCAAATCGCAT[C/T]TTGTCTGCCACGGGC | 58513 |
rs754535715 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372487 | GCGATGACCCACAGA[A/G]GACGCTGGAGCCCTC | 58513 |
rs754584112 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424421 | GGTGGGTTATGACGC[C/T]GGGTGACCTGTGCCT | 58513 |
rs754586591 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456402 | TGGCTCACGCCTGTA[A/G]TCTCAGCACTTTGGG | 58513 |
rs754588694 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381534 | GCAAGAAGGAAATGA[A/G]GTGCCATGTGACAGG | 58513 |
rs754588729 | snp | A/G | 1.69183e-05 | 0.00290841 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442253 | ATATTGGTCAAAAGT[A/G]AACACAACCCCTTGG | 58513 |
rs754626265 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411089 | AGGAAATGTCCGGAA[C/T]TCCAGGTACCTGAGA | 58513 |
rs754651853 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404623 | ACTTCTGCCGGACGT[C/T]GCTCAGCATGTCTCG | 58513 |
rs754687275 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394855 | ATGTGGGTCTTGTGG[A/T]GAGCTTGGAACACTT | 58513 |
rs754688489 | snp | A/G | 3.29516e-05 | 0.00405891 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393923 | TGGACACAGTCTAAA[A/G]ACCGGTCCGGGAAAC | 58513 |
rs754708689 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423106 | ATGAACGAGTCTCCT[A/G]TGATGTCCAAATCTA | 58513 |
rs754712971 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471608 | CTCCGGGATGCAGCC[A/C]AGCGCCTCCGCGGGT | 58513 |
rs754739966 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451230 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 58513 |
rs754748428 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378215 | AGGTAGGTAGGTAGG[C/T]AGGCACTTCCTATAG | 58513 |
rs754750487 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436192 | TGTAAACATGGGACG[A/G]AAGTGCTTGGGACCT | 58513 |
rs754765693 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419218 | TGTTCTCAACACTTT[C/G]GGAGCTGAGGCGGGC | 58513 |
rs754784810 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419958 | AGGAGAAGCAAGCTT[A/T]GGGGTGGCTCAGTCA | 58513 |
rs754848532 | snp | A/T | 1.6501e-05 | 0.00287232 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437756 | ATGTGAACTTGAAGG[A/T]CTTGGACACTCACAA | 58513 |
rs754884381 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462330 | CAGGGCTGGGGTCCC[A/G]TTGCCACCTGTTCTG | 58513 |
rs754908292 | snp | C/T | 1.67231e-05 | 0.00289159 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421314 | TGCCACCTGTCCGGC[C/T]TTACCATATGTGTGC | 58513 |
rs754931823 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365185 | GGGCTGGGAGTGGCC[C/T]TGGAAGACGGTGTGG | 58513 |
rs754943542 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445710 | CCCTCTGTATGCTGA[A/G]AGCAGCCTCTGGAGC | 58513 |
rs754943682 | snp | A/T | 1.65583e-05 | 0.00287731 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440758 | AGCCGTGCTCATGCC[A/T]AGTAATACTTGACAG | 58513 |
rs754952846 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361038 | TGTATCAAGGAAGCT[A/G]CTAAAAACTCCTTGA | 58513 |
rs754959553 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386872 | TGGCACCAAGTTAAC[C/T]GCCTGCTGAAACAAA | 58513 |
rs755004120 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360328 | AAGCAGGTTTTGTTT[C/T]TGGCTTTTATTAACA | 58513 |
rs755012255 | in-del | -/AGAAAACTACC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444099 | GAAGTGAAAGTACAG[-/AGAAAACTACC]ATGACAAAATGAAAA | 58513 |
rs755051356 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439074 | CTTGTTTTTTTTCTG[-/G]TTTTTTTTTTTTTTT | 58513 |
rs755079665 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382572 | CAGCTTTAAACAATT[A/G]AGAAGTTGCTAAAAA | 58513 |
rs755100659 | in-del | -/C | 1.72627e-05 | 0.00293786 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417919 | GAAGGGATGTCAATA[-/C]CCCCCAGGGCATGAC | 58513 |
rs755133750 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368213 | CATCCTACACAACTG[G/T]GGACACACATACACA | 58513 |
rs755164508 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376931 | GGGCGAGGGCGGGCA[A/G]GCAGGAGGCACACAC | 58513 |
rs755175174 | in-del | -/ATAATAATA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393084 | GAGCTGGATATAATA[-/ATAATAATA]ATAATAATAATAATA | 58513 |
rs755200289 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397099 | TCTTTCTTTCTTTTT[A/T]TTTTTCTGAGACAGA | 58513 |
rs755224158 | in-del | -/AA | 0.00112883 | 0.0237306 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362001 | TGGAAAGTTTAGGAG[-/AA]AAAAAAAAGGAGAAA | 58513 |
rs755226520 | snp | A/G | 0.000149297 | 0.00863865 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377130 | TACTGACCGCTGGGC[A/G]GTTTAGGCCGTGGAG | 58513 |
rs755234931 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413774 | AACGAGACCCTTACC[C/T]GCACCTCGCTGGTTT | 58513 |
rs755251497 | snp | C/T | 1.77934e-05 | 0.00298268 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413887 | AACAAGAGTGAATAA[C/T]AAGCCTCCACCCCTT | 58513 |
rs755252675 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375160 | ATGGAGAGTGTGCAC[A/G]GAGGGGTGCATGGGA | 58513 |
rs755254156 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438214 | AAAAATCAGCCAGGC[A/G]TGGTGGCAGGTGCCT | 58513 |
rs755256417 | snp | A/C | 1.70493e-05 | 0.00291965 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361858 | AATGGGTCTTTTCCA[A/C]TAAACGGGTCCCCAA | 58513 |
rs755262424 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366936 | CTTAATCGTTTTTTC[C/T]GATTTTGTGAGGTAT | 58513 |
rs755339254 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433905 | GAGGCAGAGGTTGCA[A/G]TGAGCCGAGATCGTG | 58513 |
rs755344925 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418016 | GAGGAGGGTCGATGC[C/T]TTTACTGACCTTCTG | 58513 |
rs755353067 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459500 | AGGCAGGTGGTGGGC[C/T]GAGTGCAGGAAGGTG | 58513 |
rs755383370 | snp | C/G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416914 | CAGCCCATCCAAAGC[C/G/T]CTCGTTTACACATGA | 58513 |
rs755432719 | snp | A/G | 0.000115332 | 0.00759293 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403763 | TTGCGTTGACTTCAG[A/G]GACTTGATGATGGTT | 58513 |
rs755450097 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375180 | GGTGCATGGGAGAGT[A/G]CGTGTGTGCCTGCAT | 58513 |
rs755504117 | snp | A/G | 1.68114e-05 | 0.00289921 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418101 | CCTCGTATCGGCCAG[A/G]GCCCTGGGAGAAACG | 58513 |
rs755509285 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415680 | AAGGGGCCACTGCAG[A/G]CCCCAGCCTCCTACA | 58513 |
rs755528651 | snp | A/G | 1.72764e-05 | 0.00293903 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441870 | AGCCACAGAAGAGAA[A/G]TCACTATTCATCTTC | 58513 |
rs755529867 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374459 | CCTGAAGCCAGGCCC[-/A]AGGAAGTCACCCAAA | 58513 |
rs755560486 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455266 | GGGACCATAGCCATG[C/T]ACCACCATGTGTGGC | 58513 |
rs755581228 | snp | A/G | 1.65285e-05 | 0.00287471 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377276 | GAGAGGACATGAAAG[A/G]GAGGCAAAAATAGTT | 58513 |
rs755602582 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383894 | ACCTGGGCATGGGGC[C/T]GGTGGGGCCCCGAGG | 58513 |
rs755620881 | snp | C/G/T | 6.99513e-05 | 0.00591367 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418146 | ACACATCACAGGCGC[C/G/T]GACTCAGCCTGAACC | 58513 |
rs755630724 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380449 | CATACCAATGCAGCC[A/G]TCTAAGGCTCTAGTG | 58513 |
rs755647029 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410561 | AGACAAATGTTCCTA[C/G]CAACAATATTTGCAA | 58513 |
rs755678208 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358796 | TCATTTACCGACAAT[A/G]AAATTGTATCCAACT | 58513 |
rs755682343 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379970 | CATAGACGCGGCTGT[C/T]TGAGGCTCTAGCTTC | 58513 |
rs755687420 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465728 | TTCCATGTCCCTCTC[C/T]ACCTTTTAATGAGAT | 58513 |
rs755689587 | snp | C/T | 1.65064e-05 | 0.00287279 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437750 | AGAAGAATGTGAACT[C/T]GAAGGACTTGGACAC | 58513 |
rs755722706 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359414 | GAGCTGGTTATGGAT[-/G]ATTTTAGACAATGAT | 58513 |
rs755814628 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441994 | GACCTGAAATGGGAG[A/G]CCAAGAGGCAAAATA | 58513 |
rs755870780 | snp | A/C | 2.18534e-05 | 0.00330548 | intron-variant, utr-variant-3-prime, missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361774 | AGGCGGAGGACTCAA[A/C]TTACAGAGGTGAAGT | 58513 |
rs755873691 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386774 | AAGCCTGGGGGGACT[C/T]GAGGCAGCCTGTAGC | 58513 |
rs755905497 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429415 | CAGGCTGCCAGTCCC[C/T]GGATCTAAGCAGATG | 58513 |
rs755907271 | in-del | -/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382623 | TATTTCACAGATGGC[-/T]TTTTTTTTTTTTCAG | 58513 |
rs755975353 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473947 | TTGGGCAACAAGAGC[A/G]AAACTCCGTCTCAAA | 58513 |
rs755982639 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444360 | ATGGCTGCCCCCCTC[A/G]TGCTTGGAGGCAGTG | 58513 |
rs756005566 | snp | A/G | 1.73969e-05 | 0.00294926 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413878 | TTTCATGAAAACAAG[A/G]GTGAATAATAAGCCT | 58513 |
rs756010563 | in-del | -/CAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415070 | ACTGCTGTAACAAAT[-/CAC]CAACTGGGTGGCTTG | 58513 |
rs756022019 | snp | A/G | 1.72931e-05 | 0.00294045 | intron-variant, missense | EPS15L1 | GRCh38.p7 | 19:16402313 | TAATACGTTTATTCA[A/G]CCTTTACCATGGCTC | 58513 |
rs756059149 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359229 | AGTCAGACAGCCCTC[G/T]TGGCATTTGCTCAGG | 58513 |
rs756059777 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399920 | AACCTTTCTTAATCT[A/G]TCCTCAGTAAGGCCT | 58513 |
rs756061628 | snp | G/T | 1.65102e-05 | 0.00287312 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377152 | GCCGTGGAGGAGCAG[G/T]TTTCTTCGGAGGCAG | 58513 |
rs756074772 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395452 | ATAACAAGGCTTTAT[G/T]TTTGAAAGGATCATC | 58513 |
rs756094810 | in-del | -/A | 0.010065 | 0.0702224 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362001 | TGGAAAGTTTAGGAG[-/A]AAAAAAAAAGGAGAA | 58513 |
rs756141315 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403753 | TGATTTCGTCTTGCG[C/T]TGACTTCAGGGACTT | 58513 |
rs756171413 | snp | C/T | 1.91657e-05 | 0.00309556 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386127 | GGGGAGCTCTGCTAC[C/T]GCCCAAGGAATAGTC | 58513 |
rs756173967 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366792 | CAAAGAAAGCCCCCG[G/T]CATCACTGTAGGGCC | 58513 |
rs756176656 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372290 | CCAGGTCAACACCTG[C/T]CTGCCCGTGCACCCA | 58513 |
rs756204434 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450957 | TAAATGGTACAGGCT[C/T]TTTTTTTTTTGAGAC | 58513 |
rs756224892 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378063 | GATGGAATGGTAGTT[A/G]GATGAATGGATAGAC | 58513 |
rs756259479 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462125 | CTGTTCTCCATGGGG[G/T]TCTGACCAGTTGTTT | 58513 |
rs756261464 | snp | A/G | 1.84378e-05 | 0.00303621 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386226 | ACTGGATTCAAAGGG[A/G]TCGAGCTAAATGAAA | 58513 |
rs756295906 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365800 | CAGCTCTGTGAAAAG[C/T]GGGCCCAGCATACCA | 58513 |
rs756327966 | snp | C/T | 3.29761e-05 | 0.00406041 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16440902 | TCTGGATCGGCCAAG[C/T]CCCATATCTGCGGAA | 58513 |
rs756344343 | snp | C/G | 0.000122692 | 0.0078314 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441853 | GGGGGAGCTGTGAGG[C/G]CAGCCACAGAAGAGA | 58513 |
rs756348557 | snp | C/T | 1.66015e-05 | 0.00288105 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425124 | GGGACAGGCTCCCTG[C/T]GCTGTTGAGGCTGCT | 58513 |
rs756360891 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419538 | AGGCCTTTGGCATCT[A/G]TGAAAAATGTCTTCC | 58513 |
rs756412137 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419172 | CACAATCAAGGAGCC[A/G]GCCAGGGCCGGGTGC | 58513 |
rs756414720 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383682 | TCAGAAGTGGGATCT[C/G]CTGCGCCGCCAGGGC | 58513 |
rs756418565 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377532 | CTAGCACCAAGGGCA[A/T]CCCCAGTCACACGAG | 58513 |
rs756438586 | snp | C/T | 0.00011792 | 0.00767762 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425208 | CAGGCAGGACGGGGA[C/T]GGCGCCAGGGAACAC | 58513 |
rs756453569 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377327 | TGTCCACTGAACAGA[C/T]GCTCATGCTCCAAGG | 58513 |
rs756472198 | snp | C/T | 1.66252e-05 | 0.00288311 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434479 | CCCATCAAATTTGGC[C/T]TTTTCTTCCACCTAG | 58513 |
rs756498753 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470111 | ACCTGGCCAGGCGCA[A/G]TGGCTAACGCCTGTA | 58513 |
rs756507720 | snp | A/C | 1.68071e-05 | 0.00289884 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361960 | AAGTCTGCGGAACCA[A/C]GCTGGCTTACAGGTG | 58513 |
rs756518941 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466948 | AGCACATGCGTCACA[C/T]GGCAGGGTCCTGACA | 58513 |
rs756525555 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406929 | TGAGTGGGATTAGTG[A/G]CCTTATAAAAGAGGC | 58513 |
rs756563120 | in-del | -/AC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437711 | TACACACATGCACAT[-/AC]ACACACACACACATC | 58513 |
rs756577022 | in-del | -/TCA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375226 | CACATGCGAGAATAC[-/TCA]TGTGATGCAGTATGT | 58513 |
rs756604732 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382275 | ATTTCCGAATCCCAA[C/T]TTTCATGACTTCAAG | 58513 |
rs756621716 | snp | A/G | 0.000100022 | 0.00707113 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403714 | TGGCATGTGGCAGGG[A/G]CCCGACTCCGTGAAG | 58513 |
rs756621961 | snp | A/G | 1.64917e-05 | 0.00287151 | stop-gained, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418001 | CCGGCGAGAGGACTT[A/G]AGGAGGGTCGATGCC | 58513 |
rs756665344 | snp | C/T | 1.74695e-05 | 0.00295541 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377071 | GAGGCCCTGGTCCCC[C/T]GCCATCCGGCACCGG | 58513 |
rs756728581 | snp | A/G | 0.000189807 | 0.00974 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355676 | CTGGAACCCGCCCGT[A/G]CCCTGTCCCGCCTAC | 58513 |
rs756797597 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464016 | GGACTGCAGGCCTGG[A/G]AAACACGGGGAGCAG | 58513 |
rs756804168 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379123 | CCCAGCTAATACGGT[A/G]AAAAACCCCATCTCT | 58513 |
rs756806132 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391265 | ATAGAAAACAAGCAG[C/T]AGAGAAAAATGAAGC | 58513 |
rs756834397 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433602 | GCTGAGGTGGGAGGA[G/T]GGCTTCAGCCTGGCA | 58513 |
rs756869570 | snp | A/C | 3.29897e-05 | 0.00406125 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436963 | AGTGGGCCTCTGCAG[A/C]GGGCGGTGTGACCAT | 58513 |
rs756894012 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404265 | GGGATCTGTGAGGAG[C/T]CTCAGAGACACCTGA | 58513 |
rs756906563 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431086 | TCTACTAAAAATATA[A/C]AAATTAGCTGGGCGT | 58513 |
rs756929013 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389677 | AAATTGTAACAGTCT[C/T]ATGGAGTTTCTAATG | 58513 |
rs756957700 | snp | A/G | 1.66944e-05 | 0.0028891 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437029 | AAACATTCCTTTGTG[A/G]CTGGCACAGAATTAA | 58513 |
rs756958823 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361496 | GTGCGTCAGAAATAA[C/T]ACAATGAATCTACCG | 58513 |
rs756964819 | snp | A/G | 1.6498e-05 | 0.00287206 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377251 | AAGGGCCAGAAGGTG[A/G]GGGCTGTAAGAGAGG | 58513 |
rs756971503 | in-del | -/TTCC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418613 | CAGCAACGACTCTCT[-/TTCC]TTGTTATGAACGGAA | 58513 |
rs756973133 | snp | A/C | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361509 | AATACAATGAATCTA[A/C]CGTGAAGGACAGATA | 58513 |
rs756973939 | snp | C/T | 1.72365e-05 | 0.00293563 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418134 | GGGATGCTAATTACA[C/T]ATCACAGGCGCCGAC | 58513 |
rs756994627 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428886 | ACGGCAGTCAATATA[C/T]ATTTCAGGACCAGTC | 58513 |
rs757000362 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446943 | TGCAGGAAGTTAGGC[A/G]TATAACACTGAAACA | 58513 |
rs757010112 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443077 | GCTGTAAAAGTTTAC[A/G]TGCGTTGGTGTTTTA | 58513 |
rs757016033 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399611 | TTCCTGTGGTGTAAA[C/T]AGTCTCATCATGGTT | 58513 |
rs757029937 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358139 | GCCTTTGGCCCCACT[A/G]AGCCCCCGTGTCACA | 58513 |
rs757038650 | snp | G/T | 7.17965e-05 | 0.00599109 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386199 | GGAGACACTGGAGGA[G/T]GAAAAGGGATCACTG | 58513 |
rs757046993 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456353 | GGATACAAAAGTGTG[C/T]AGGACAGAGTCCTGG | 58513 |
rs757058311 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441516 | TGCCTGTAATCCCAG[A/C]TATTCAAGAGGCTGA | 58513 |
rs757058906 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389313 | TAAAACAATAGCTGG[A/G]TGTGGAGGTACATGC | 58513 |
rs757061419 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427575 | ACATACAAAGAACTA[C/T]GTCAAGACAAACACT | 58513 |
rs757098880 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370421 | AAGGGGTTGAGGTGT[A/C]CTGGAGGCAGGTACA | 58513 |
rs757113259 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454021 | TGAAACAATACAAAC[G/T]GGCATTCCTTTAGAA | 58513 |
rs757115152 | snp | C/T | 1.66076e-05 | 0.00288158 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425089 | GCTCCGTACCTGTGT[C/T]TGCTTGAGGCTGTGC | 58513 |
rs757129826 | snp | G/T | 5.03242e-05 | 0.00501593 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425199 | GGGGGCTGGCAGGCA[G/T]GACGGGGACGGCGCC | 58513 |
rs757138373 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410469 | CAGCTCCTCAACAGT[C/T]ACCATGTGGCCCAGC | 58513 |
rs757148309 | snp | C/T | 3.29973e-05 | 0.00406172 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413761 | TGTAACCAAAACGAA[C/T]GAGACCCTTACCTGC | 58513 |
rs757148781 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386860 | CTGCAGTGTGAGTGG[C/T]ACCAAGTTAACTGCC | 58513 |
rs757175147 | snp | C/T | 5.04096e-05 | 0.00502018 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404774 | AGTTGCAGGGGTTTA[C/T]GTGAGGATGGGAAAA | 58513 |
rs757195003 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414365 | CTTGACCTCAGCCTG[G/T]GACACCCTGGACAGC | 58513 |
rs757239390 | snp | C/T | 0.000347102 | 0.0131693 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355880 | ACGGAGAGTGGGTGA[C/T]GTGGCCCTGGGGCTG | 58513 |
rs757279165 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463165 | AATGTGGGGTCTCAC[A/G]TGGCTTGGAGGGTTT | 58513 |
rs757282944 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405778 | CATGAACAGCACCTC[C/T]GGGGATGGGGACACC | 58513 |
rs757353762 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386484 | TGAAGGCTGGGAAGT[A/G]AACAAGACAGGAAGA | 58513 |
rs757395662 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460451 | TAAAGGACATTTTCT[A/G]GTGGCTAAGAGTCAA | 58513 |
rs757400772 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473776 | CCAGCCTGGCCAACA[C/T]GATGAAATCCCGTGT | 58513 |
rs757407541 | snp | C/T | 1.66785e-05 | 0.00288773 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402454 | TGGGCCTCCTGGCGG[C/T]TTTCATGCAGCTGGG | 58513 |
rs757416952 | snp | C/G | 1.66098e-05 | 0.00288177 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403694 | TCTTGGGGCTCGCTG[C/G]TCCCTGGCATGTGGC | 58513 |
rs757432058 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376241 | TTAGAGAATAGGAGG[A/C]GTCCCAGACCGGGGC | 58513 |
rs757437526 | snp | A/G | 1.65343e-05 | 0.00287521 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385256 | ACAGGTCTTTAAGAG[A/G]ACATGCCTTCTGGGG | 58513 |
rs757448952 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459851 | AAATCACAGTCCTTA[C/T]AGCCTGCCCTGCCAA | 58513 |
rs757464613 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396869 | AACAACACACAAGGT[A/G]TGATTCCACTTCTAT | 58513 |
rs757510517 | in-del | -/TGTG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375467 | GTGATTATGCATATA[-/TGTG]TGTGTGTGTGTGTGT | 58513 |
rs757516915 | in-del | -/AAAT | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473961 | CGAAACTCCGTCTCA[-/AAAT]AAATAAATAAATAAA | 58513 |
rs757584638 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429337 | AGCACCATCACGCTG[A/C]CAGCTTCCTGACCCA | 58513 |
rs757592411 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381670 | CTGCCCCAGTTGTCC[C/G]CAGGCCTGTCCGAGA | 58513 |
rs757599084 | in-del | -/AAAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387896 | AGAAAAAAGAATGAA[-/AAAT]AAATAAATAAATAGA | 58513 |
rs757627929 | snp | G/T | 3.34694e-05 | 0.00409067 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442228 | TGGGAATCTGTAAAT[G/T]AAACCACAGATATTG | 58513 |
rs757647851 | snp | C/G | 3.29652e-05 | 0.00405974 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392392 | AAGTCGTCAGTGGCA[C/G]AGCCACGGAATGGGT | 58513 |
rs757659508 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437705 | TGCACATACACACAT[G/T]CACATACACACACAC | 58513 |
rs757662954 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379171 | TTAGCCGGTCGTGGT[A/G]GCGGGCGCCTGTAGT | 58513 |
rs757701099 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467029 | TGAGAAAACTAAGGT[A/G]CAGAAAGTATTTGCA | 58513 |
rs757731667 | snp | A/G | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355102 | ACCAGCCTGGGCAAC[A/G]TGGCAAGATCTCATC | 58513 |
rs757748689 | in-del | -/AAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449249 | TCTGATTTCTTAAAA[-/AAC]AAACAAACAAACAAA | 58513 |
rs757783117 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366768 | TTGCTAATGACCAGA[C/T]GCTTTGAGCAAAGAA | 58513 |
rs757790767 | snp | A/G | 3.29576e-05 | 0.00405928 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434428 | GACTTTGTCTCCAGA[A/G]AGCAAACCATTGATG | 58513 |
rs757792715 | snp | A/G | 1.67891e-05 | 0.00289729 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417646 | AACTGTCCTAGAATT[A/G]AATTCAGAGGCGAGA | 58513 |
rs757793647 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393931 | GTCTAAAGACCGGTC[C/T]GGGAAACACTGAATT | 58513 |
rs757804323 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436763 | TTCATTAGAAGAGGC[A/G]TTTCATCCAAGTGCT | 58513 |
rs757809274 | snp | G/T | 3.29511e-05 | 0.00405887 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393910 | TCTGAGCCAGGACTG[G/T]ACACAGTCTAAAGAC | 58513 |
rs757841102 | snp | A/G | 1.64743e-05 | 0.00287 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361943 | GATCGGGGGCCTCGG[A/G]AAAGTCTGCGGAACC | 58513 |
rs757843840 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432569 | CGAGACTCTGTCTCA[A/G]ATAAATAAATAAATA | 58513 |
rs757854108 | snp | C/T | 3.29946e-05 | 0.00406155 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404727 | AAACTGCTTGTTTCC[C/T]GGTCTAGGTCATTTT | 58513 |
rs757896514 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470831 | TGATGACAGTAATTA[C/T]AGGATCACTGAGTGC | 58513 |
rs757906056 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469364 | GGAGGATCGGCTGCA[C/G]CCACAGGGCACCGGG | 58513 |
rs757926643 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360412 | ACTCACTGCCGTTGT[A/G]AAATATTTATAGGTC | 58513 |
rs757948890 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409148 | ATGCAGGAGGATCCC[A/T]TGAGCCCAGGATTTT | 58513 |
rs757952780 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403219 | ACGGCTGCAGGCCAC[A/G]AGAAGCCAGCGCCCC | 58513 |
rs757953417 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361116 | CAAAGCCAGGCTTTC[A/G]AAATCCCGAGATTTG | 58513 |
rs757958991 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445090 | CTGTGATTCCAGTGG[A/G]AAAAAAAGAGTTTCA | 58513 |
rs757986257 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445859 | GCCGTAGGAATGGAA[G/T]GAAGTGCAGCAGAGC | 58513 |
rs758023196 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415254 | CAGACCCGATCTGCC[A/G]GTATCTGGAGGTTGG | 58513 |
rs758039179 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457260 | TGTGGAGGTGAACAA[C/T]GGGACATTCCCCACC | 58513 |
rs758079325 | snp | A/G | 1.689e-05 | 0.00290598 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402484 | GAAAGTTTGCTCCTT[A/G]CCTGTGCAACAAAGA | 58513 |
rs758113498 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372543 | TTTTTTAACGGAAAA[C/G]ATTTCCACTAAACTG | 58513 |
rs758158925 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436943 | TTCACTTACCCTCAC[A/G]GCCCAGTGGGCCTCT | 58513 |
rs758172166 | in-del | -/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375469 | GATTATGCATATATG[-/TG]TGTGTGTGTGTGTGT | 58513 |
rs758198515 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379060 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 58513 |
rs758220381 | snp | A/G | 3.33017e-05 | 0.00408041 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403690 | CGGCTCTTGGGGCTC[A/G]CTGGTCCCTGGCATG | 58513 |
rs758224468 | snp | C/T | 1.65034e-05 | 0.00287253 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385138 | CTTTACCTTGGACAT[C/T]TGGCTGAAGTCGGCA | 58513 |
rs758229065 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362079 | GCACAAGCCCGGGGC[G/T]CTTCTCTGAGAAAAG | 58513 |
rs758252837 | in-del | -/AGAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389921 | TAATAAAAGGCCAAT[-/AGAC]AGAATTCAAAAAAAC | 58513 |
rs758306949 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392937 | GTATCAGCTACTAAG[A/G]AGGCTGAGGCAGAAA | 58513 |
rs758308516 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389743 | CATAAGACATGCTGG[C/T]TGCAAGGGTGGGTGG | 58513 |
rs758315872 | snp | A/C | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421461 | CTGCCACGGGCACCA[A/C]CCAGTTCACTGTTGG | 58513 |
rs758362663 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420019 | CTCTGCTGACCCGTA[C/T]GGTGGCAGCCATCGC | 58513 |
rs758362799 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433468 | GCATAAAATTTTTCC[C/T]AAATTTGCAGCAGAG | 58513 |
rs758382227 | snp | A/T | 4.95495e-05 | 0.00497718 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385239 | CCAACAAAGTCAGAG[A/T]TACAGGTCTTTAAGA | 58513 |
rs758426778 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459559 | AGCTCTGTGGCTCAG[C/T]AGCAGTGAGGACAAG | 58513 |
rs758458244 | snp | C/T | 0.00018494 | 0.00961435 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428707 | CAGGACTTACCACAG[C/T]GAACTCATCTCGATC | 58513 |
rs758464310 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389274 | AGCCTGGCCAACATA[C/T]GGAAATCCCATCTCT | 58513 |
rs758479774 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472552 | ACTGAGGCAGGAGAA[C/T]TGCTTGAGCCCAGGA | 58513 |
rs758483983 | in-del | -/CTT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452130 | GGCTACAGAGTGAGA[-/CTT]CGTCTCAAAAAAAAA | 58513 |
rs758491557 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429228 | CCACTCCCCAGCAGT[A/G]GATGGTGAGACAGGT | 58513 |
rs758513492 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399584 | AAAGCCCTGGTTTAG[A/G]GCTTCTGCCAATTCC | 58513 |
rs758552953 | snp | A/C | 1.67936e-05 | 0.00289767 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417513 | TGGGAGAGTTCGTGT[A/C]ACATCTGGATGTGGA | 58513 |
rs758574585 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437785 | AAATTTAGGCGGTGG[C/T]ATGCTCAAATTCAGA | 58513 |
rs758597320 | in-del | -/GAC | 1.66479e-05 | 0.00288508 | cds-indel, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425140 | GCTGTTGAGGCTGCT[-/GAC]GCTGCCGTGGGACGG | 58513 |
rs758606485 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372674 | CAGAAGCCTGCGTCC[C/T]GGTCCCTGTGCCGCA | 58513 |
rs758629718 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436529 | TGGCTGGAAAGAAGC[A/G]AGAAAGCAAGGGACA | 58513 |
rs758639737 | snp | G/T | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403881 | AGATCGTCTTCCTGG[G/T]ACTTTAAGTCAGATT | 58513 |
rs758639764 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465871 | AACTTTCCAAGACAA[G/T]AAACTATGGTGCAAT | 58513 |
rs758649244 | snp | A/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384038 | CCCCCACACCGGCCA[A/C]CCCTTACCACCTGGG | 58513 |
rs758658583 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357275 | ACACTCTAGACTTTT[C/T]CCCCCCCAGGCCTGT | 58513 |
rs758664001 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398450 | CACACGCCCAGCAAG[C/T]GTCTGATGGGGGTCT | 58513 |
rs758682473 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369139 | AGACACATGAGGGGA[A/G]TTTGTTTTTTACAAT | 58513 |
rs758706169 | snp | A/G | 1.65669e-05 | 0.00287805 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402438 | CTGCTCCAGGCTCCT[A/G]TGGGCCTCCTGGCGG | 58513 |
rs758719816 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364987 | TGACACCCCAGTCTT[A/G]TCCAGGTGGCACCTC | 58513 |
rs758726798 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441329 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGT | 58513 |
rs758728046 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392565 | GAACGCTAGTGACGG[A/C]AAACAGGATAATGGT | 58513 |
rs758750301 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449335 | GCAAAAAGACATTTT[A/C]CCAAAGAGGAAATAT | 58513 |
rs758773804 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422508 | TATCTAGATGATGAG[A/G]GAGTGGAGAGAAAAA | 58513 |
rs758784318 | in-del | -/ACAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368220 | CACAACTGTGGACAC[-/ACAT]ACACAACCATCATTG | 58513 |
rs758797263 | snp | C/T | 3.29804e-05 | 0.00406068 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392295 | CGGGCAACGTCCCAC[C/T]CCACTCACCTTCGAA | 58513 |
rs758850975 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405643 | CCTTGGCCATGGAAC[A/G]GGATGGCGCCGTGTG | 58513 |
rs758882445 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363925 | ACAGAAGGACTCGGA[C/G]ACAAACTCCCCTGCA | 58513 |
rs758889629 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461798 | CTGACTGCTGTCACC[A/G]GCCAGTGGGCTCGAG | 58513 |
rs758909838 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448272 | GTGGTGGTTCATGCC[G/T]GTAATCCCAGCACTT | 58513 |
rs758934876 | snp | C/T | 4.985e-05 | 0.00499225 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442206 | GATTCATACAACGAA[C/T]TTCCAGTGGGAATCT | 58513 |
rs758941455 | snp | C/T | 9.95768e-05 | 0.00705539 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404555 | GCCCCTGCCTGTGCA[C/T]AGGGCGCTGCCCCGG | 58513 |
rs758944442 | snp | G/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356068 | GGACGGGATGCATGT[G/T]ATTGAGTGTGACCTT | 58513 |
rs758957356 | snp | A/G | 1.8405e-05 | 0.00303351 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361802 | AGTCTGCAAAGCCCG[A/G]GGCAGAGGCCTTAGA | 58513 |
rs758961656 | snp | G/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392372 | TCTTTGTCTGTTTCT[G/T]GAAGAAGTCGTCAGT | 58513 |
rs758970581 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416060 | TTTTCTAACCAGCCA[C/T]CCACCTTGATCCCCT | 58513 |
rs758978426 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356665 | GCACTTACACTGCCA[C/T]TTAGTCAAGTTTTTA | 58513 |
rs758988763 | snp | A/C/T | 5.42887e-05 | 0.00520979 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386175 | ATGGGTCTCACCTGA[A/C/T]CCTTTTGAGGAGACA | 58513 |
rs758988775 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382154 | CCCATGTGTGTTTAA[A/T]CCCACGAGGCCAATT | 58513 |
rs759015104 | snp | C/G | 1.65064e-05 | 0.00287279 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385228 | TGCAATCGGCACCAA[C/G]AAAGTCAGAGTTACA | 58513 |
rs759029215 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469763 | CACCTTCACCTGGCC[A/G]TCTGCTTGCCAAGTG | 58513 |
rs759035922 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468436 | CTGCAACCTCCGCCG[A/C]CTGGTTTCAAGCGAT | 58513 |
rs759038349 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376109 | CTGATGGAAAGGGCT[C/T]GGGGGCATGCCCTAT | 58513 |
rs759100262 | snp | C/G/T | 4.94689e-05 | 0.00497317 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440839 | CCAGCCCCTCCATTT[C/G/T]CTCTGTGTACATGTG | 58513 |
rs759111850 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425991 | CTTGCCAGATTAAGG[C/T]GAGACTCATCAGCGA | 58513 |
rs759115960 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358924 | TTCCTAATACACACA[-/G]TTTGCCTGAGACAGA | 58513 |
rs759119728 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404709 | TGAGCCTCGAGCTCC[C/T]GCAAACTGCTTGTTT | 58513 |
rs759133910 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451915 | GGTCGAGGCAGGCAG[C/T]TACCTGAGGCTGGGA | 58513 |
rs759138939 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442567 | GGAAAGGACACTCTA[C/T]CCTCTGAGATTGTTC | 58513 |
rs759198243 | snp | C/T | 4.99921e-05 | 0.00499935 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425158 | GCTGCCGTGGGACGG[C/T]GTGGAGCGGAGGCTG | 58513 |
rs759204165 | snp | A/G | 4.9812e-05 | 0.00499034 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434352 | AGAAGAACCAAGCCC[A/G]TGGCCCACTTACCCT | 58513 |
rs759219909 | snp | C/T | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354934 | CTTATGGGAACTCTT[C/T]GTATCTTTGTGATTT | 58513 |
rs759262730 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437553 | AAAAGTTCTGGAGCT[A/G]GACAGAGGTAATGAA | 58513 |
rs759265656 | snp | C/G | 1.66971e-05 | 0.00288934 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361923 | AGCCCCGAGTGGCTG[C/G]AATGGATCGGGGGCC | 58513 |
rs759307325 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366638 | GTTTTCAGAAGGAAC[A/G]TCAACAACAACAACG | 58513 |
rs759312624 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433421 | ACGGGCGTGAGCCAC[C/T]GCACCAGGCTAAGAC | 58513 |
rs759325514 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374190 | CATGACCTCCCTCCC[C/T]GCCTTTCCTCTTCCA | 58513 |
rs759353583 | snp | A/G | 1.76061e-05 | 0.00296694 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361992 | ACTTTTACCTGGAAA[A/G]TTTAGGAGAAAAAAA | 58513 |
rs759405493 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362331 | TTAACATACTAATTT[A/T]AAAAATCATGGCTGA | 58513 |
rs759428631 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373615 | ACACTCATCTGCTGA[C/G]CGCTCTTGCCCATAA | 58513 |
rs759473502 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403043 | GTGGCCTATAAACTG[A/G]CTAATGGAGCACAGA | 58513 |
rs759494164 | snp | G/T | 1.6495e-05 | 0.0028718 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403969 | TTAAAGAGATTCACA[G/T]TGCAGGATGAAATGG | 58513 |
rs759507010 | snp | G/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383081 | AGAGCTGCAAGGTCA[G/T]GGTTGAGCTCAGAAT | 58513 |
rs759513718 | snp | A/G | 1.73027e-05 | 0.00294127 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417913 | GCGGTGGGAAGGGAT[A/G]TCAATACCCCCAGGG | 58513 |
rs759549161 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458326 | TGGTTGCTGCCACCA[A/T]GGAGCATCATAGTCA | 58513 |
rs759556721 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415082 | AATCACCAACTGGGT[A/G]GCTTGGAACAGGAAA | 58513 |
rs759560843 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426650 | TCTCAAAAACAGAAC[A/C]ACGACAACAAAAAAA | 58513 |
rs759603812 | snp | A/G | 3.30764e-05 | 0.00406659 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417976 | CCTCTCTCCGAAGGC[A/G]GGACCATGTCCGGCG | 58513 |
rs759605386 | snp | A/G | 1.72311e-05 | 0.00293518 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402518 | CATCAGCATTAAGCA[A/G]GGTCAGGAAAACATG | 58513 |
rs759626120 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454715 | AACCAACAAGCAAGA[G/T]AACTGCCCCGAGCAT | 58513 |
rs759626687 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410230 | TTCTCCAATGACTAC[A/G]TACAAATGGCTAATA | 58513 |
rs759637963 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378682 | CTGGGGGGATGCTTG[C/T]CCCTCACTTGGAGCG | 58513 |
rs759642029 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369095 | CTTTTCCCCAACACA[C/T]GTCAACGTCTTCCTC | 58513 |
rs759646781 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470081 | AAGGAACAGGAAGAG[A/G]CTAAGAAGTCAGTGA | 58513 |
rs759672933 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445704 | AAAGAGCCCTCTGTA[C/T]GCTGAGAGCAGCCTC | 58513 |
rs759682385 | snp | C/T | 9.03138e-05 | 0.00671928 | utr-variant-5-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16471951 | GCGCCGCCATCTTCC[C/T]GCGGACTCGGGCTCC | 58513 |
rs759729762 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392361 | AAATGGGTCATTCTT[C/T]GTCTGTTTCTTGAAG | 58513 |
rs759747889 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465185 | CACATGCAGCCATGG[A/G]TTGGACAAGCTTGGC | 58513 |
rs759752925 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421839 | CCCACTTGGAAGGAC[C/T]GTCCCTGGAGAACCG | 58513 |
rs759756571 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434581 | GCCAAGTGAAAATGG[C/T]CACGGACCCATCATC | 58513 |
rs759781225 | snp | A/C | 3.30207e-05 | 0.00406316 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404582 | CCGGAGGTGGCCGGG[A/C]CCCACCATCTGAGTC | 58513 |
rs759802806 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464703 | TCCCTGGGCCACACT[A/G]GAATTGTCTTGGGCC | 58513 |
rs759812003 | snp | A/G | 2.10307e-05 | 0.00324267 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428682 | CCTGGGCTGGGTGGG[A/G]AGGAAACAGCAGGAC | 58513 |
rs759817887 | snp | A/T | 1.68434e-05 | 0.00290197 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392473 | CCATAAGTAAACATT[A/T]TACCAAGTGAAAGAA | 58513 |
rs759893307 | in-del | -/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383245 | CTGAAATCACAGCTG[-/C]CATGTGTGTGAAGAG | 58513 |
rs759955089 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359753 | TGAGGTCCCAGCTAC[A/G]TGGGAGGCTGAGGTG | 58513 |
rs759962656 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473426 | GGCAGGAGAATTGCT[C/T]GAACCTGGGAGGGGA | 58513 |
rs759963511 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363566 | CCTTGTGGGCTCCGG[A/G]GCTACAGCCCCCATC | 58513 |
rs759987704 | snp | A/C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443571 | AAAAATTAGCCAGGC[A/C/G]TGGTGGCATGCACCT | 58513 |
rs759996791 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385810 | CCTTCAAACACAGAA[C/T]CCACAACATAGGCCA | 58513 |
rs760003590 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472216 | CTTCCAACGTTGTTC[A/G]GACTCTCATGCCGCT | 58513 |
rs760017294 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411291 | GTAGTTGCCAGGGGC[C/T]GGAGAAAGGGGAGAA | 58513 |
rs760032001 | snp | C/G/T | 3.30635e-05 | 0.00406581 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385093 | GAGGCACAAAGACAC[C/G/T]AGCAGAGGCGCGGGG | 58513 |
rs760058634 | snp | G/T | 1.7318e-05 | 0.00294256 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417910 | CAGGCGGTGGGAAGG[G/T]ATGTCAATACCCCCA | 58513 |
rs760069683 | snp | A/G | 0.000148384 | 0.0086122 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377236 | CCAAGGAGGAGGTGA[A/G]AGGGCCAGAAGGTGG | 58513 |
rs760069805 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391540 | GCAGGCCCCGGGCCT[A/G]GGTTGCAGCCTAGAA | 58513 |
rs760078743 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394449 | AGGGGCTGCCAGATT[C/T]GCCTCTCAGACCCGG | 58513 |
rs760102629 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360572 | CACAGCAAGACCCTA[C/T]CTCTACAAAAAAAAA | 58513 |
rs760107330 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366531 | ACCAAGAACTGCCTG[G/T]GCCTGGTTTTGCTCT | 58513 |
rs760120096 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466636 | GGCCAGGCGCGGTGC[C/T]TCCTGCCTGTAATCC | 58513 |
rs760128183 | snp | C/T | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354873 | TGACAGAGCTCAGAC[C/T]CTGTTTCAAAAAAAA | 58513 |
rs760136821 | in-del | -/GC/TGTGCG | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472434 | GTGTGTGTGTGTGTG[-/GC/TGTGCG]CGCGCTAATTTGGGG | 58513 |
rs760154534 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449981 | CAGAGTGGTGGTTGC[C/T]GGGGATAAGGAAGAG | 58513 |
rs760185534 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391894 | GCTGTGTGTTACAAG[A/G]ACCGTGCAGGGTGGC | 58513 |
rs760190116 | snp | A/G | 3.29881e-05 | 0.00406115 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402390 | CAGGTCGGTCAGGCT[A/G]GCACCATGGGCTCCA | 58513 |
rs760200312 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371161 | TTTTGGGACCCACAT[-/G]GGGCACATGATGGGG | 58513 |
rs760228261 | snp | C/G | 1.7525e-05 | 0.0029601 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437885 | AAGTCCAAAGAAAGG[C/G]AAGGAGTAAACAGCA | 58513 |
rs760252587 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421429 | CTTCAGGAATATCTC[A/G]TCAAATCGCATCTTG | 58513 |
rs760275569 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418253 | CTTCCCTACTTCACA[A/T]CTCCTTCCCAGGAAG | 58513 |
rs760277399 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406246 | GAAGCTGGGGTCTCC[A/G]TTCCCCAGTCTCCCT | 58513 |
rs760279189 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460993 | TAAAATTGAAAAGCA[C/G]GTCCTCTTCAGATTA | 58513 |
rs760297835 | snp | A/G | 9.91621e-05 | 0.00704068 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385105 | CACTAGCAGAGGCGC[A/G]GGGGCTCCGTGGAGG | 58513 |
rs760307150 | in-del | -/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369678 | GGAAGAAAAAAAAGT[-/GT]GTGTGTGTGTGTGTG | 58513 |
rs760332077 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437354 | CAACATGGATGAACC[C/T]TGAAAACACGATGCT | 58513 |
rs760332867 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418522 | GTAGCTCTGGGTCAT[C/G]TGAATGGCCCCGGCT | 58513 |
rs760359987 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364852 | GCCTCATCTCCCTAT[C/T]GGCCGCCCACCAGCT | 58513 |
rs760376128 | snp | A/C/T | 4.94803e-05 | 0.00497374 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440831 | GGCTCTGCCCAGCCC[A/C/T]TCCATTTGCTCTGTG | 58513 |
rs760379245 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445607 | GTTGCTAATGACATA[A/T]ATCCCCAGCCCCAGG | 58513 |
rs760387729 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385217 | CCAAAGGGATCTGCA[A/G]TCGGCACCAACAAAG | 58513 |
rs760412952 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376767 | GCTGCCGGCCATGAG[C/T]GGCTCCTGAAGTATA | 58513 |
rs760455569 | in-del | -/ACAAATAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432592 | AATAAATAAATAAAT[-/ACAAATAC]AAATACAAATACAAA | 58513 |
rs760463185 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466312 | TGACCGGGAGGATGA[A/C]CCAGGCAATCTATGA | 58513 |
rs760507020 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467906 | TTTCTGTGGGTCTTG[A/G]TTTCCTCACTTGTAA | 58513 |
rs760552580 | in-del | -/TT | 8.35806e-05 | 0.006464 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442012 | AAGAGGCAAAATAAC[-/TT]TTCAGCAAATGCAGC | 58513 |
rs760593205 | snp | A/G | 1.65381e-05 | 0.00287555 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442151 | GCATGCTCTAGTTCC[A/G]TCTGAAGAGACATCA | 58513 |
rs760604098 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464568 | ACCCCAAAGTCCCAG[A/C]CGCATGTTTTGGCCC | 58513 |
rs760607128 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382105 | ACCCTCCAGGCTGAC[C/T]GGGGACACCTCGGGC | 58513 |
rs760611261 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413282 | GCTGGTGTAACTCAT[C/T]CCCACGCCCAGGGGC | 58513 |
rs760635223 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468227 | CTCACAGTGATGTTC[C/T]AGCAACCGGAGCAAC | 58513 |
rs760656632 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374637 | CAGACCCAGCGCCGG[G/T]TTTAGGTACGTGGGG | 58513 |
rs760681240 | snp | C/T | 2.14273e-05 | 0.0032731 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428669 | TGCACATTTCCTTCC[C/T]GGGCTGGGTGGGGAG | 58513 |
rs760689609 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424249 | GGGGAGCATGTGGAC[C/T]GTAGGCCCCCAGAAA | 58513 |
rs760693087 | snp | C/G | 3.33045e-05 | 0.00408058 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418087 | AACTTCCCCGTTTGC[C/G]TCGTATCGGCCAGGG | 58513 |
rs760728687 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396407 | GCCAGGACTATAGGC[A/G]CGCACCACCAAGCCT | 58513 |
rs760738929 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452530 | GAAGCTAAGGCAGGA[G/T]GATTGCCTGAGGCCA | 58513 |
rs760752856 | in-del | -/TCGGTTCAGCTCCGACTTGGC | 1.64737e-05 | 0.00286994 | cds-indel, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403838 | TTCCTCCTGCTGCAA[-/TCGGTTCAGCTCCGACTTGGC]TCGGTTCAGATCGTC | 58513 |
rs760761681 | snp | C/T | 9.88445e-05 | 0.0070294 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437079 | GCTGAAAAGGATACA[C/T]GTTTCAAAGTGCTTT | 58513 |
rs760766729 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448566 | GGGGGGAGAAAGGCC[A/G]GGCGCGGTGGCTCAC | 58513 |
rs760770218 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378715 | GGTGAGGCACAGGGG[A/T]GCCAGGGTCTCCATC | 58513 |
rs760777209 | snp | A/C | 1.64833e-05 | 0.00287078 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377209 | AGGGGTCATCTGAGA[A/C]TCCTGCCCCTCCCAA | 58513 |
rs760815665 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432209 | GAGGCCGAGGCAGGT[C/G]GATCACCTGAGGTCA | 58513 |
rs760820359 | in-del | -/GTG | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472836 | CAAAAATTAGCAGGT[-/GTG]GTGGTGCATGCCTGT | 58513 |
rs760846016 | snp | A/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472390 | CCGCAAAGCGCCCTG[A/T]TCCTAGGATCGCAGT | 58513 |
rs760861917 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463494 | AACCCAGCTCCAAGC[A/G]CTCCCTGTGTAAGCA | 58513 |
rs760913136 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446498 | TATAATCCCTTGTTT[C/T]CTATCCAGTACCTCT | 58513 |
rs760916905 | snp | A/C | 1.73447e-05 | 0.00294483 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421273 | TCTTCACCCACAGGC[A/C]CCCTGGAGCCACCCA | 58513 |
rs760941695 | snp | C/G | 1.85637e-05 | 0.00304656 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403940 | TGAGATCTGAAATGA[C/G]ATGTTAAAAGATGTT | 58513 |
rs761025060 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374635 | AGCAGACCCAGCGCC[A/G]GGTTTAGGTACGTGG | 58513 |
rs761046638 | snp | A/G | 5.55247e-05 | 0.00526871 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361757 | GGAGTGGGGTGGCCC[A/G]GAGGCGGAGGACTCA | 58513 |
rs761050703 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358549 | GACACCGTAGGGGCA[G/T]GACACCACCCTAGCC | 58513 |
rs761056945 | snp | A/C/G | 0.000148878 | 0.00862662 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413744 | ATTTAGCACAAAGTA[A/C/G]ATGTAACCAAAACGA | 58513 |
rs761064480 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440953 | ATGACTGCCGATCAC[C/T]GTCCACGTGTTAACA | 58513 |
rs761096311 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421664 | TGAGGCTGAGACAGG[C/T]TGAGGCTGGCTCTGT | 58513 |
rs761096767 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399225 | GGTCAGGGTAACTAA[G/T]AGTGGTTTTGATTCC | 58513 |
rs761106397 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453413 | GCCATCAACTTTTAA[C/T]GTGTTTAAAGGCCAT | 58513 |
rs761118329 | in-del | -/AAAATTTTG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408488 | AATACAAATTTTTAC[-/AAAATTTTG]TAAAAATACAAAAAT | 58513 |
rs761149334 | snp | C/T | 1.65263e-05 | 0.00287452 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395506 | ACAGGGATTTTATTA[C/T]TTCTGAGTTAAAGCA | 58513 |
rs761149463 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364143 | GACTCACATGGATGA[A/G]AAAGAGGGGAGGTCG | 58513 |
rs761176123 | snp | C/T | 2.15269e-05 | 0.0032807 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428661 | CTGCGCACTGCACAT[C/T]TCCTTCCTGGGCTGG | 58513 |
rs761196301 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405460 | TGGATCCAGATGGTC[A/C]GCCCGAGGCTCCAAT | 58513 |
rs761220366 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366314 | AGCGACTGCCACGGT[A/G]CAGAAGGTTCAAATA | 58513 |
rs761222396 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395386 | GGTCAGATTTGAAGG[A/G]GTCTTCTGTCTGGAA | 58513 |
rs761226639 | snp | C/T | 3.30464e-05 | 0.00406474 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436926 | GGAGGGAGCTATTCC[C/T]GTTCACTTACCCTCA | 58513 |
rs761230108 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394895 | TCTTGATGCCTTGGC[A/T]CTCTGGTTAACAGGG | 58513 |
rs761265634 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376595 | CTCACATCAGATGCC[A/G]CCAAGGACAATCTCC | 58513 |
rs761285628 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368043 | TTATACAGTTCAGTT[A/C]AGTGCTGTACTTGGA | 58513 |
rs761320949 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417380 | CAAATGGAAGATGTC[A/G]TTCTTCAAGCCCCTT | 58513 |
rs761336271 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367088 | AGAGAGCTTTACTGA[C/T]GCGCATTTCAGAAAA | 58513 |
rs761339017 | snp | A/T | 1.67801e-05 | 0.00289651 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413853 | ATTTCTCTCTGAATG[A/T]TTAAAAATATTTCAT | 58513 |
rs761343550 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417580 | CAATCTCTTGACTGA[C/T]GTCATCAAGCTCCTT | 58513 |
rs761348291 | snp | A/G | 3.45167e-05 | 0.00415417 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361840 | GCTGCAGAGGAGGGG[A/G]CAAATGGGTCTTTTC | 58513 |
rs761348500 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363551 | TGAGGCCCCAGGTGT[C/T]CTTGTGGGCTCCGGG | 58513 |
rs761370045 | in-del | -/AGAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471383 | CGAATTTGAGGACAC[-/AGAG]AGGCGCCCGGAGACG | 58513 |
rs761401721 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449014 | CATGGTGGTGCGTAC[C/T]TGTAGTCCCAGCACT | 58513 |
rs761402804 | snp | G/T | 3.30322e-05 | 0.00406387 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437736 | ACACATCTGGTATTA[G/T]AAGAATGTGAACTTG | 58513 |
rs761427985 | snp | C/T | 1.76593e-05 | 0.00297142 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402296 | ACCAGAGCCCCATAC[C/T]GTAATACGTTTATTC | 58513 |
rs761454886 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460246 | CCGTGATGGCACCAC[C/T]GCACTCCAACCTGGG | 58513 |
rs761463557 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459867 | AGCCTGCCCTGCCAA[C/T]TGATCTTTGCCAAGC | 58513 |
rs761476579 | in-del | -/TTCA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378266 | AAGGCATGCAGGGAC[-/TTCA]TCGCTGCCCCAGCTG | 58513 |
rs761504460 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395082 | AAAATTAGCCGGGTG[C/T]GGTGATGGGCGCTGA | 58513 |
rs761516124 | snp | C/G | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402377 | CGCTCAGGTTGGCCA[C/G]GTCGGTCAGGCTGGC | 58513 |
rs761519990 | in-del | -/T | 6.59294e-05 | 0.00574111 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395296 | ACTCTAAATTCGACA[-/T]TAAAACACACAGTCT | 58513 |
rs761522186 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392214 | GGCACCATGTACGCT[A/C]CACGAAGGGAAGGGG | 58513 |
rs761567133 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411725 | TTATTTTTGAGGCAG[A/G]GTCTCACTCTGTTGC | 58513 |
rs761592265 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420934 | CCTCACCCTGCCAGG[C/T]CACTCTGCTAGAGGC | 58513 |
rs761619315 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445472 | AGAAGGGGGAAGAAA[C/G]AAGGTACAGCACCAG | 58513 |
rs761635852 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378487 | GCTGGACCCCACTGC[C/T]GTCCCCCAGAGCTCT | 58513 |
rs761635857 | snp | A/T | 1.64988e-05 | 0.00287213 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392272 | ACAGAGCAGGCACGC[A/T]GCTCTCCCGGGCAAC | 58513 |
rs761716251 | in-del | -/G | 1.8405e-05 | 0.00303351 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361802 | GTCTGCAAAGCCCGA[-/G]GGCAGAGGCCTTAGA | 58513 |
rs761733744 | snp | C/T | 7.43356e-05 | 0.00609609 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362028 | AGAAAGAAAGAAATA[C/T]GAGTTACTCACCCGG | 58513 |
rs761775585 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380357 | AAGGCTCTAGCGTCT[A/G]GTCACACAGACACAG | 58513 |
rs761794439 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408204 | CAAAGACCCACCAGC[C/T]CGAGGTTAGGAAGGG | 58513 |
rs761813050 | snp | C/T | 0.000113977 | 0.00754821 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425268 | GGGACGGGGGCAGGG[C/T]GGAGGGCACGGGCTC | 58513 |
rs761817351 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436119 | TCTTCATGTCCTCTC[C/G]CTGCACAGATACCCC | 58513 |
rs761875292 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424951 | CAGGCGTGAGCCACC[A/G]CACCTGGCCACAAGC | 58513 |
rs761910127 | snp | A/G | 2.60474e-05 | 0.00360874 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361761 | TGGGGTGGCCCGGAG[A/G]CGGAGGACTCAACTT | 58513 |
rs761916250 | snp | C/G | 1.64784e-05 | 0.00287035 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395332 | TGAGAAAGTGGGTAG[C/G]AAGTGAGATACCTTT | 58513 |
rs761927152 | snp | C/T | 3.32265e-05 | 0.0040758 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436897 | TGGAACAATTCTATC[C/T]GAAGGAGAGCCAAGG | 58513 |
rs761932115 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360108 | AACGAGCCCTTTGCG[G/T]GTTGGGGTCACAGGA | 58513 |
rs761957638 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401829 | CTTGAAAGAGCAACA[C/T]CCTGGGGCGCTGCTT | 58513 |
rs761958142 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360859 | GACATGGCAGGGCTG[C/T]GTTCAAAGAGCCATC | 58513 |
rs761974614 | snp | G/T | 1.69172e-05 | 0.00290832 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377105 | GCGGTGGCTGCGAGA[G/T]AAGAAAGCTTACTGA | 58513 |
rs761974634 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387603 | CAAGAGTGAAACTCC[A/G]TTTGAAAAATAAATA | 58513 |
rs761977905 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399664 | GCTCACAAGTTCCTG[-/T]TTTTTTGCTTTTTGG | 58513 |
rs761984660 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359763 | GCTACGTGGGAGGCT[A/G]AGGTGGGACGATTGC | 58513 |
rs761990824 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445573 | CTGATATGTCATTGC[A/G]ACAGAACTGAAGACA | 58513 |
rs762034901 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430684 | GGTCCACTGCAGGCT[C/G]TGAAAAATGCTTACT | 58513 |
rs762082372 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413071 | GCACCAGGTTCAAGG[C/T]GTTTGTTGCTATCGG | 58513 |
rs762086353 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373032 | ACAAACCCTGGATGG[C/G]AGCATGGGACATCAG | 58513 |
rs762160564 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453368 | CCGGGGCCTCCCACG[A/G]TGCTGGGATTATAGG | 58513 |
rs762171353 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378518 | CCCAGGGCTCTCCCT[A/G]GGGCTGCTTCCTGCC | 58513 |
rs762187527 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407582 | CCGCCAGACTCAGTC[C/T]CCCAAAGTGCTGGGA | 58513 |
rs762192773 | snp | A/G | 3.34348e-05 | 0.00408855 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425058 | GTGCTCTGAGAGGGG[A/G]CTGTGCCCGCTGAGG | 58513 |
rs762195222 | snp | A/G | 0.000183268 | 0.0095708 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355686 | CCCGTGCCCTGTCCC[A/G]CCTACACACGGCCCT | 58513 |
rs762217487 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408361 | AGGCACGGTAGCTCA[C/T]GCCTGTAATGCCAGC | 58513 |
rs762304014 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446809 | GAAGAGGTCAAAAGG[C/T]AACACTCAATTTGAG | 58513 |
rs762351521 | in-del | -/AT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407729 | GGTAATTTTTTGCAC[-/AT]AGTTTCTCCCCCATT | 58513 |
rs762372387 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420636 | GAGGTATTTGCCTCT[C/T]GAGAATTATCCAGCA | 58513 |
rs762379868 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438304 | GCTGCAGTGAGCCAA[C/G]ATCATGCCACTTCAC | 58513 |
rs762399850 | snp | C/G | 1.6674e-05 | 0.00288734 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425173 | CGTGGAGCGGAGGCT[C/G]TCTTTTGGTGGGGGG | 58513 |
rs762445473 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398890 | CAGCCCAGAACTCCC[A/G]GGCTCAAGGATCCTC | 58513 |
rs762450559 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378025 | ACAATTGGATAGATG[A/C]ATGGATGGTGGGTGG | 58513 |
rs762462486 | snp | C/T | 0.000162853 | 0.0090222 | synonymous-codon, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16355768 | GTCCTCCTGCTCCTG[C/T]CGCCGCAGCCGCGCC | 58513 |
rs762466002 | snp | A/C | 1.66012e-05 | 0.00288103 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413725 | GGAAGTTTTCCTGAA[A/C]TACATTTAGCACAAA | 58513 |
rs762470191 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393988 | TGCAAAGGGGTCATT[C/G]TGGAACGGGTCGCCT | 58513 |
rs762488898 | snp | C/G | 1.65021e-05 | 0.00287241 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392266 | TACCACACAGAGCAG[C/G]CACGCAGCTCTCCCG | 58513 |
rs762526029 | in-del | -/AGTCAG | 3.30142e-05 | 0.00406276 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385231 | AATCGGCACCAACAA[-/AGTCAG]AGTTACAGGTCTTTA | 58513 |
rs762534709 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383420 | CGACAACCAGAAACG[A/G]CCAGGACGCCTGAGG | 58513 |
rs762536911 | in-del | -/AATAATAATAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393116 | AATAATAATAATAAT[-/AATAATAATAAA]CAACGCAGGTAAATC | 58513 |
rs762561004 | snp | C/G | 3.30464e-05 | 0.00406474 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413752 | CAAAGTAGATGTAAC[C/G]AAAACGAACGAGACC | 58513 |
rs762567661 | in-del | -/C | 0.000185684 | 0.00963366 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355683 | CCGCCCGTGCCCTGT[-/C]CCGCCTACACACGGC | 58513 |
rs762568075 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395413 | GGAAAGGATCCGGAT[C/G]CAACTCTTGCGTGTT | 58513 |
rs762600976 | snp | A/C/T | 1.64887e-05 | 0.00287125 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440853 | TGCTCTGTGTACATG[A/C/T]GTATATACCTGTTTG | 58513 |
rs762666013 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469940 | GGCCTGGGAGGGCCA[C/T]GCCTCACACCTGGGC | 58513 |
rs762685438 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360831 | GAAACAAATCGGGTG[-/C]TTTCTGTGCATTGAC | 58513 |
rs762694391 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357508 | TTGGCAGCGTCTGGA[A/T]ATTTCACGGCTTGAT | 58513 |
rs762714425 | in-del | -/CA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432593 | ATAAATAAATAAATA[-/CA]AATACAAATACAAAT | 58513 |
rs762734471 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397981 | ACTCACAAACCAGTC[C/T]AGTATTCCAACCGAC | 58513 |
rs762788070 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440851 | TTTGCTCTGTGTACA[C/T]GTGTATATACCTGTT | 58513 |
rs762864737 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392211 | GCAGGCACCATGTAC[A/G]CTCCACGAAGGGAAG | 58513 |
rs762915702 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390880 | GTTGCTTTAAATTTA[C/T]ACAGATGCTCCTTGA | 58513 |
rs762917821 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404888 | CAGGGCCAGCATTCC[A/G]TGCACACCCACGGCC | 58513 |
rs762920420 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375696 | AAATGATCTCTTTAC[A/G]CATCTGTATCTGCTC | 58513 |
rs762934228 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450602 | TCTCCTGCCTCAGCC[A/T]CCCAAGTAGCTGGGA | 58513 |
rs762937540 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363399 | ACCTGCCCCGCCCAC[C/G]ACCTGAGCCTGGGAC | 58513 |
rs762953509 | snp | C/T | 3.29859e-05 | 0.00406102 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440959 | GCCGATCACTGTCCA[C/T]GTGTTAACAAAAACC | 58513 |
rs762954673 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403744 | GTACCTGGTTGATTT[C/T]GTCTTGCGTTGACTT | 58513 |
rs762998338 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412825 | GGACAGCACCGGAGC[C/T]GGGACCAAGGCCACG | 58513 |
rs763020731 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358713 | CCTGTCCTCACTGGC[A/G]CTCCAAGGTGTCTGA | 58513 |
rs763044271 | snp | C/T | 3.58976e-05 | 0.00423645 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386191 | CCTTTTGAGGAGACA[C/T]TGGAGGATGAAAAGG | 58513 |
rs763065357 | snp | A/G | 1.67424e-05 | 0.00289326 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361935 | CTGGAATGGATCGGG[A/G]GCCTCGGGAAAGTCT | 58513 |
rs763090514 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404688 | CGGTCTTGAGCATCC[C/T]GTTTCTGAGCCTCGA | 58513 |
rs763111177 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430009 | CAAAAATGTCCCCAG[A/G]CATTGCCCAATGTCC | 58513 |
rs763120037 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443740 | AAAAATAATAATGCC[C/T]GGATTATGGTCAGCG | 58513 |
rs763122394 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380271 | ATGCAGCCATCTAAG[C/G]CTCCAGCATCTAGCC | 58513 |
rs763125374 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411534 | AACACGGTGATTATG[C/T]GAAACACCACTGAAA | 58513 |
rs763132938 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444063 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs763175124 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442918 | GGCCACCAGAGGCCA[C/T]ACCTGGATCCAGCCT | 58513 |
rs763175159 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455901 | CCTCCCCCCACCCTT[C/T]GCATAAAACCTCCTG | 58513 |
rs763176294 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422826 | AGCCAGGTGTGGTGG[A/T]AGGCACCTGTGATCC | 58513 |
rs763189053 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437482 | TGCCAGCGACTGGGA[C/G]GGGGAGACAAGGAGT | 58513 |
rs763212838 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393952 | ACACTGAATTTTACC[C/T]GTTGAAGTTGTCTGC | 58513 |
rs763223336 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380953 | AGAGTCGAGGTTGCT[C/T]GGCCCAGTCAGAGCC | 58513 |
rs763233543 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434401 | CAGCTTTGAGTTCAT[A/G]AGGACTGGCTTGACT | 58513 |
rs763249853 | snp | A/G | 1.69395e-05 | 0.00291024 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417939 | CAGGGCATGACCAGC[A/G]CCACTCACCGGGCCG | 58513 |
rs763286636 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410598 | AACATCTATCAATGA[-/G]GGATGGATGAGTAAA | 58513 |
rs763308881 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387341 | GGCAAGGCACAGTAG[C/T]TCATGCCTGTAATCC | 58513 |
rs763333461 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473084 | GTCCTCAACCTTGGC[C/T]CAAACTCTCTACTTA | 58513 |
rs763346139 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360240 | GTGTGAAGAGTTCTG[-/T]TTTTTTTTAAATCAG | 58513 |
rs763366986 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461671 | TTTTCTACAGATTGG[C/T]GTAATGACAGAGGCA | 58513 |
rs763374491 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430489 | GTGGAGGGGTGTGAG[A/G]CACAGTCCTTAACAG | 58513 |
rs763394870 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473054 | GCAACTTGAATCTGT[A/G]TCTCCTGGACTGCGG | 58513 |
rs763422718 | snp | C/T | 1.6666e-05 | 0.00288664 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437858 | AGTCTCAGTGCAACA[C/T]AGAAACCCTGCAAGT | 58513 |
rs763437415 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413049 | AAACAGACCCGCGCC[A/G]GCCAGTGCACCAGGT | 58513 |
rs763437798 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401630 | CTGGTGTGAACAGGG[C/G]GGATGTGACCACCTA | 58513 |
rs763442584 | snp | A/G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377899 | CTGGCCCGGACCCTC[A/G/T]GTCAGCCTCCATCAC | 58513 |
rs763472142 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448036 | GGGCACTGGAGCAAT[C/T]GGCATCCATAGGAAA | 58513 |
rs763494171 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415338 | AGAGTGGTTTGTTAT[A/G]GCAGTATGAATGGAC | 58513 |
rs763506006 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431800 | GTATCAAACCACCAC[A/G]TGGACCCCACACTAC | 58513 |
rs763530571 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385292 | GGGAAATGCTAGATG[A/G]CCCCTGAACCAGGAG | 58513 |
rs763551199 | snp | A/G | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421411 | ATCCAGGTCCAGGTC[A/G]GTCTTCAGGAATATC | 58513 |
rs763567632 | snp | A/G | 1.64844e-05 | 0.00287087 | stop-gained, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404614 | CATCCTGGCACTTCT[A/G]CCGGACGTCGCTCAG | 58513 |
rs763612650 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433473 | AAATTTTTCCTAAAT[G/T]TGCAGCAGAGTTGAA | 58513 |
rs763635120 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415303 | CTGTGCGAAATGTCT[A/G]ATGTTTCAGTCACCC | 58513 |
rs763645556 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364363 | CTCTCCTTCCGACAG[C/T]GCCTGCCCTCTCAGG | 58513 |
rs763645860 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374863 | TGTATGAGCACACAC[A/G]CACGCATATGTGTGT | 58513 |
rs763650747 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459187 | CATGGTTATGCGGTG[C/T]GTGACTGCATTCCCT | 58513 |
rs763672438 | snp | C/T | 1.65367e-05 | 0.00287543 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413840 | TGTTCCAGTGAATAT[C/T]TCTCTCTGAATGTTT | 58513 |
rs763674054 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446831 | CAATTTGAGCATATA[A/T]ATGGACTTGAAAGCC | 58513 |
rs763680860 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391988 | GGGGGCAGATGACTA[G/T]AGTTGAGGGGTAGGA | 58513 |
rs763762414 | snp | A/G | 0.000463442 | 0.0152153 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402278 | CTGCTGTCACACCAG[A/G]GGACCAGAGCCCCAT | 58513 |
rs763768683 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418295 | TTCCCCGCTCCCAGT[A/G]TCCCCCACCCTAGGA | 58513 |
rs763776025 | snp | C/T | 4.99023e-05 | 0.00499486 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403692 | GCTCTTGGGGCTCGC[C/T]GGTCCCTGGCATGTG | 58513 |
rs763784411 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426845 | TTAGATAATAATAGA[A/C]ACGCTCATACAGAAT | 58513 |
rs763795002 | in-del | -/A | 0.000169334 | 0.0091999 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355860 | GCCAAACTGCAAAGG[-/A]AAAAACGGAGAGTGG | 58513 |
rs763810372 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422832 | GTGTGGTGGTAGGCA[A/C]CTGTGATCCCAGCTA | 58513 |
rs763858590 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416518 | TGGCATGCACCTGTA[C/T]TCTCAGCTTCCTGGG | 58513 |
rs763874622 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464822 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 58513 |
rs763890581 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469954 | ATGCCTCACACCTGG[A/G]CCAACAGTAACCCAT | 58513 |
rs763898665 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357536 | GATGGTGGCATGAGC[A/G]GGAAGCAGGAGAGAG | 58513 |
rs763909103 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435054 | GTTCAAGCAATTCTC[A/G]TGCCTCAGCACTCGT | 58513 |
rs763968468 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374641 | CCCAGCGCCGGGTTT[A/G]GGTACGTGGGGAGGC | 58513 |
rs764018439 | snp | A/C/G | 3.29692e-05 | 0.00406001 | missense, synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403745 | TACCTGGTTGATTTC[A/C/G]TCTTGCGTTGACTTC | 58513 |
rs764029598 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392231 | ACGAAGGGAAGGGGG[C/T]CTTCGGGAAGCGCCA | 58513 |
rs764051492 | snp | A/G | 8.31677e-05 | 0.00644802 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425079 | CCCGCTGAGGGCTCC[A/G]TACCTGTGTTTGCTT | 58513 |
rs764066412 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386310 | ACCAGACCTTCCTGA[C/T]GTCGATGTACAACAT | 58513 |
rs764070106 | snp | A/G | 1.79425e-05 | 0.00299515 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386193 | TTTTGAGGAGACACT[A/G]GAGGATGAAAAGGGA | 58513 |
rs764120479 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393980 | TGCTGTTCTGCAAAG[A/G]GGTCATTCTGGAACG | 58513 |
rs764122170 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400997 | AAAGTAGGAGCCGGG[C/T]TGTGAGACGGAAACA | 58513 |
rs764153572 | snp | C/T | 0.000146843 | 0.00856737 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16471987 | CCGGGGGAACGGGGG[C/T]GGGGCTGCAGCCACG | 58513 |
rs764156318 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391198 | GTAACCCCAAATAAA[C/T]AGGAGTAAGGAAATG | 58513 |
rs764160214 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404961 | CCAGCTCCCTCAGCA[C/G]GTATTTCCCGATGGC | 58513 |
rs764162027 | snp | A/G | 0.0001628 | 0.00902073 | missense, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16355773 | CCTGCTCCTGCCGCC[A/G]CAGCCGCGCCAGCCT | 58513 |
rs764172046 | snp | G/T | 6.6024e-05 | 0.00574523 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434413 | CATGAGGACTGGCTT[G/T]ACTTTGTCTCCAGAG | 58513 |
rs764175501 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371610 | TTAGCGGTAGAACTG[C/T]GCTGGCTGGTGTCAC | 58513 |
rs764208074 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455998 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 58513 |
rs764261073 | in-del | -/CAAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387765 | AGCGAGACTCTGTCT[-/CAAA]CAAACAAAAAAAAAC | 58513 |
rs764281025 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429231 | CTCCCCAGCAGTGGA[C/T]GGTGAGACAGGTGTC | 58513 |
rs764312395 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407207 | GCTCAGGGTACCTCA[C/T]CACTTCTCTAAGAGG | 58513 |
rs764327039 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411602 | TAGCCATCCTTCAGA[C/T]TGGTATTAAAATTTG | 58513 |
rs764333018 | snp | A/G | 0.000121946 | 0.00780757 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437882 | TGCAAGTCCAAAGAA[A/G]GGGAAGGAGTAAACA | 58513 |
rs764340890 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379075 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT | 58513 |
rs764387656 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370256 | GTGGCAGGCAAGGGG[C/T]GCGCTGACTCAGGGC | 58513 |
rs764399173 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442985 | CTGAGCTCTGCCAGA[C/T]GTCTCCCAGGGAAGG | 58513 |
rs764401858 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399595 | TTAGAGCTTCTGCCA[A/G]TTCCTGTGGTGTAAA | 58513 |
rs764491740 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410168 | ATTTAAAAATCGGCA[A/G]GAAAAAAATTTTTTC | 58513 |
rs764523778 | snp | C/T | 1.68883e-05 | 0.00290584 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421305 | AGCCACAACTGCCAC[C/T]TGTCCGGCCTTACCA | 58513 |
rs764537875 | snp | A/C | 1.66299e-05 | 0.00288352 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442209 | TCATACAACGAATTT[A/C]CAGTGGGAATCTGTA | 58513 |
rs764589731 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406476 | CAGAGAGAGCCTGAG[A/G]TAGCCCAATGCTCCG | 58513 |
rs764611844 | snp | A/G | 4.97698e-05 | 0.00498823 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404559 | CTGCCTGTGCATAGG[A/G]CGCTGCCCCGGAGGT | 58513 |
rs764613797 | snp | A/G | 4.94238e-05 | 0.00497086 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421420 | CAGGTCGGTCTTCAG[A/G]AATATCTCATCAAAT | 58513 |
rs764635698 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460431 | AATGTGCATTAAATG[G/T]GAATTAAAGGACATT | 58513 |
rs764642629 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365102 | CATCACAGGCAGTGG[C/G]CTTCTCAGGGAAGAA | 58513 |
rs764659391 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449343 | ACATTTTACCAAAGA[C/G]GAAATATAGCAGATG | 58513 |
rs764688883 | snp | G/T | 8.23784e-05 | 0.00641735 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393900 | ACATGCGACTTCTGA[G/T]CCAGGACTGGACACA | 58513 |
rs764705945 | in-del | -/AAACA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432773 | GAGACTCTGTCTCAC[-/AAACA]AAACAAAACAAAACA | 58513 |
rs764720931 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432961 | AGTCACGCACCACCA[A/C]ACCTGGCTAGTTTTT | 58513 |
rs764721243 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383134 | GGCAGCTGATGGAAC[A/G]CTGGAATCAAAACAA | 58513 |
rs764763768 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424459 | AGTTTGGCCCCACTA[C/G]CTTCGTTGCCAGTAA | 58513 |
rs764775520 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415107 | AGGAAAAATTGATTA[C/T]AGGTGTGAGCCACAA | 58513 |
rs764794852 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373627 | TGACCGCTCTTGCCC[A/G]TAACCAGAGGCCTCC | 58513 |
rs764811924 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367206 | TCCTGGCACCTGGTT[C/T]GATGCCATCAATCCT | 58513 |
rs764818877 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395139 | GGCGGAGGTTGCAGT[A/G]AGCCGAGATTGCGCC | 58513 |
rs764829232 | in-del | -/AAATAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432594 | TAAATAAATAAATAC[-/AAATAC]AAATACAAATACAAA | 58513 |
rs764876855 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468703 | AAGGTTTTTGGAACA[A/G]GGGAATATGTTTTAG | 58513 |
rs764895825 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414005 | GTACAGTCCCTTCCC[C/T]GTCAACTGTAGGTAG | 58513 |
rs764906991 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420977 | CTGCCCGCACCTCCC[A/G]GAGGCGGCTGTGACA | 58513 |
rs764964505 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394025 | AAGAGGAGAGAAATG[C/T]TTATTAGCTCTAGGG | 58513 |
rs764976815 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389242 | GGAGGATTGCTTGAG[C/T]CTAGGAGTTTGAGAC | 58513 |
rs765027498 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433422 | CGGGCGTGAGCCACC[C/G]CACCAGGCTAAGACT | 58513 |
rs765040784 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420869 | TGTGCTCACCCTCCC[A/G]CCAGGAGCCAAAGCA | 58513 |
rs765050854 | snp | C/T | | | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392307 | CACCCCACTCACCTT[C/T]GAAGGTAAGGAAGGG | 58513 |
rs765054072 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416642 | ACTCTGTCTCAAATT[-/A]AAAAAAAAAAAAAAA | 58513 |
rs765060849 | snp | C/T | 1.65756e-05 | 0.00287881 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434358 | ACCAAGCCCGTGGCC[C/T]ACTTACCCTGCCCAG | 58513 |
rs765090082 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360666 | ACAGGAGGATCGCTT[A/G]AGCCCAGGAATTCGA | 58513 |
rs765115151 | snp | A/G | 3.31192e-05 | 0.00406921 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440759 | GCCGTGCTCATGCCT[A/G]GTAATACTTGACAGT | 58513 |
rs765115797 | snp | C/G | 1.65086e-05 | 0.00287298 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385232 | ATCGGCACCAACAAA[C/G]TCAGAGTTACAGGTC | 58513 |
rs765127863 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458328 | GTTGCTGCCACCATG[A/G]AGCATCATAGTCAGG | 58513 |
rs765157670 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463892 | AGGGTTTGGAAAGAG[A/C]ATTCCAGAGAGAGGG | 58513 |
rs765165899 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404077 | CACCTGGCTTCCTTA[C/T]AGGCCTCTTTCTACA | 58513 |
rs765179114 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427083 | AGGGCGAGAGAGTGA[C/T]GGAGGGAGGGAGGAA | 58513 |
rs765190445 | snp | C/G | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402413 | GGGCTCCATCGAGCA[C/G]CTGGTCATACTGCTC | 58513 |
rs765198154 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446850 | GACTTGAAAGCCAGT[-/G]TTTTCGATGACCTGC | 58513 |
rs765201284 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445736 | GGAGCTGCCCACCCA[C/T]GTCTGACCCCAAAGT | 58513 |
rs765248798 | snp | C/T | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16442197 | TTGTAATAAGATTCA[C/T]ACAACGAATTTCCAG | 58513 |
rs765266245 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370141 | GGGGAGCAAGTGAGG[C/T]GCAGAGCCCACCAGG | 58513 |
rs765272349 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445628 | CAGCCCCAGGCAGTC[G/T]GTCACTGGCCCCTGT | 58513 |
rs765292313 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403074 | CAGAGACCAGTTCAA[C/T]TGGTAAAAGAAGTGT | 58513 |
rs765301892 | snp | C/G | 3.30136e-05 | 0.00406273 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404584 | GGAGGTGGCCGGGAC[C/G]CACCATCTGAGTCTC | 58513 |
rs765322622 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442784 | TTCCCACCAGGGAAG[C/G]AAGGAAGTGCAGTGT | 58513 |
rs765338193 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392363 | ATGGGTCATTCTTTG[C/T]CTGTTTCTTGAAGAA | 58513 |
rs765338717 | snp | C/T | 2.0708e-05 | 0.0032177 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428697 | GAGGAAACAGCAGGA[C/T]TTACCACAGCGAACT | 58513 |
rs765345838 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399466 | TTCTTAGGAAATACA[C/T]ACGGCAACTCTGAAA | 58513 |
rs765412491 | in-del | -/CTCTACTA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408454 | ATGGTGAAACCCAGT[-/CTCTACTA]AAAATACAAATTTGT | 58513 |
rs765421062 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454776 | GACATGGACCAGGAA[C/G]GTCGTCAGAACACAG | 58513 |
rs765428165 | snp | C/T | 1.69928e-05 | 0.00291481 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361863 | GTCTTTTCCACTAAA[C/T]GGGTCCCCAAACCCC | 58513 |
rs765443779 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408484 | TAAAAATACAAATTT[C/T]TACAAAATTTTGTAA | 58513 |
rs765460043 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461602 | ACTCCAGCCTGGGTC[-/A]CAGAGTGAGACTCTG | 58513 |
rs765471857 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409008 | GGGAAGATCCCTAGA[G/T]GCCAGGTGTTTGAGA | 58513 |
rs765477692 | snp | A/G | 0.00144683 | 0.0268574 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361924 | GCCCCGAGTGGCTGG[A/G]ATGGATCGGGGGCCT | 58513 |
rs765496563 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379712 | ACACCAATGCAACCA[C/T]CTAAGGCTCCAGCGT | 58513 |
rs765556597 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453831 | AATATGCACATGTAC[G/T]CTCTGTATCTACAAT | 58513 |
rs765576625 | snp | C/T | 5.10191e-05 | 0.00505044 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418115 | GGGCCCTGGGAGAAA[C/T]GTGGGGATGCTAATT | 58513 |
rs765610984 | in-del | -/ACGAGAA | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401161 | CCTCATTACGAGTCC[-/ACGAGAA]AAGAGAGTATGGGAG | 58513 |
rs765647333 | snp | C/T | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417573 | AACTGGGCAATCTCT[C/T]GACTGATGTCATCAA | 58513 |
rs765666346 | snp | A/C | 1.66228e-05 | 0.0028829 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437021 | AGAGAGAGAAACATT[A/C]CTTTGTGGCTGGCAC | 58513 |
rs765667749 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473454 | GGAAGGTTGCAATAA[A/G]CTGAGAACTCACCAT | 58513 |
rs765690488 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376799 | CCAGGGCGTCGGGGT[A/G]GCACTGACATGCTCA | 58513 |
rs765742320 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428993 | ATAATCATATTGATT[A/G]TAAGATTATAAGTTT | 58513 |
rs765772177 | snp | A/C | 1.73881e-05 | 0.00294852 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421288 | CCCCTGGAGCCACCC[A/C]CAGCCACAACTGCCA | 58513 |
rs765772304 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382161 | GTGTTTAAACCCACG[A/G]GGCCAATTGGCAACT | 58513 |
rs765780194 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472332 | CAGTGCGCCTGGGGA[A/G]GCGGTCGCCCACCCC | 58513 |
rs765787759 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460117 | CTAGCCCTACAAAAA[G/T]TAAAAATCAGAAAAT | 58513 |
rs765793463 | snp | A/T | 4.9836e-05 | 0.00499154 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404545 | TCCTTGGGAAGCCCC[A/T]GCCTGTGCATAGGGC | 58513 |
rs765797931 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396476 | ACTATGTTGCCAGGG[C/T]TGGTTTTGAACTCCT | 58513 |
rs765845007 | snp | A/G | 1.65231e-05 | 0.00287424 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385108 | TAGCAGAGGCGCGGG[A/G]GCTCCGTGGAGGGGC | 58513 |
rs765889425 | snp | C/G | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16354874 | GACAGAGCTCAGACC[C/G]TGTTTCAAAAAAAAA | 58513 |
rs765934954 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466672 | CTTTGGGAGGCTGAG[A/G]CAGACAGATCACTTG | 58513 |
rs765948803 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435860 | CTGACTCCTCTCTGC[A/G]AGGTCCCCAGGCCCC | 58513 |
rs765949441 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394503 | CTCAAGCTCCCGCTG[C/T]CCTCTCCCCACCTCA | 58513 |
rs765951004 | snp | G/T | 3.42777e-05 | 0.00413977 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402512 | AGACATCATCAGCAT[G/T]AAGCAGGGTCAGGAA | 58513 |
rs765959094 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364906 | ACCCACCCAGCAAAG[A/T]GGCCTCAACACAGGT | 58513 |
rs765967062 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392523 | ATCACAGAATGATGC[C/T]GTTTACATGAAATTC | 58513 |
rs765967700 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438348 | AAAAGAGCAAAACTC[C/T]GTCTCAAAATAAATA | 58513 |
rs765991620 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371291 | CCTGTGTGGCACCCC[C/T]GGCAGGGAGGTCAAG | 58513 |
rs765998650 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423070 | AGACTGGGAAACAAT[C/G]GTTAAACTCGTTTAC | 58513 |
rs766015013 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366578 | TTATTTAGAAATCAT[C/G]ACTATGGTAATATGA | 58513 |
rs766019098 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421432 | CAGGAATATCTCATC[A/G]AATCGCATCTTGTCT | 58513 |
rs766032830 | in-del | -/GAAAAAAAGGGTTGCCCCCTCAATTTT | 1.75472e-05 | 0.00296198 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442270 | ACACAACCCCTTGGG[-/GAAAAAAAGGGTTGCCCCCTCAATTTT]GTCATGACCAAAATA | 58513 |
rs766040077 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406327 | ACTTATGGACATGTT[C/T]GACAGGAAACTCAGG | 58513 |
rs766107550 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387774 | CTGTCTCAAACAAAC[A/G]AAAAAAAACCCCACT | 58513 |
rs766109620 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462108 | TGGTCTGATTCAGAC[A/G]CCTGTTCTCCATGGG | 58513 |
rs766122216 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436274 | TGAGGAAATGTGACA[A/G]TCTGAAAGTGAAGGG | 58513 |
rs766125826 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446516 | ATCCAGTACCTCTCA[C/T]CCTCCCGACAACGCT | 58513 |
rs766145789 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432291 | ATACAAAAATTGGCT[A/G]GGCATGGTGGCTCAC | 58513 |
rs766169372 | snp | C/T | 1.654e-05 | 0.00287571 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442153 | ATGCTCTAGTTCCAT[C/T]TGAAGAGACATCAGC | 58513 |
rs766204574 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413294 | CATCCCCACGCCCAG[A/G]GGCACTGGCATTGTC | 58513 |
rs766242583 | snp | C/T | 1.70723e-05 | 0.00292162 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361856 | CAAATGGGTCTTTTC[C/T]ACTAAACGGGTCCCC | 58513 |
rs766247419 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402397 | GTCAGGCTGGCACCA[C/T]GGGCTCCATCGAGCA | 58513 |
rs766278173 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468324 | AGGTTAGGTGGAGTC[A/G]ATTCAGGGCTTACTA | 58513 |
rs766322142 | in-del | -/CATT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358774 | TGCCTAGCCACTTCC[-/CATT]CATTCATTTACCGAC | 58513 |
rs766323483 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439378 | ATTTATTTTCCATAG[G/T]AATTCTCAGAACTTT | 58513 |
rs766338139 | snp | A/G | 1.75576e-05 | 0.00296285 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413883 | TGAAAACAAGAGTGA[A/G]TAATAAGCCTCCACC | 58513 |
rs766338264 | snp | A/G | 0.000105611 | 0.00726598 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428679 | CTTCCTGGGCTGGGT[A/G]GGGAGGAAACAGCAG | 58513 |
rs766341241 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456325 | CTGAACTCGTGCTAA[A/G]AGGCAGCACTGAGGA | 58513 |
rs766357805 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376669 | GACCAAGCAGCGACT[C/T]CTGCCACCCTCACCC | 58513 |
rs766366083 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368174 | TTATCCTATACAACA[C/T]AGAACGATCACACAA | 58513 |
rs766368537 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373362 | TGTGCTGGCCGTGTG[C/G]TCTCCCTGAGCAGAA | 58513 |
rs766372567 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360235 | AGTCATGTGTGAAGA[A/G]TTCTGTTTTTTTTAA | 58513 |
rs766380547 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452634 | GCAAAATGTCATCTG[A/G]AAAAAAAAAAAAAAA | 58513 |
rs766423515 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420776 | CAGCCCTATGAAGTC[A/G]GCTGTGTCCAGCCCT | 58513 |
rs766438871 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453429 | GTGTTTAAAGGCCAT[C/T]TGGGCTGGGCACAGT | 58513 |
rs766445395 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379588 | CCAGCATCTAGTCAC[A/G]CCGATGCAGCTGACT | 58513 |
rs766446531 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421090 | TAAGACGGACCAGAG[C/G]CCCTTCCTACTGAAA | 58513 |
rs766476971 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433267 | CAAGTGTCTGGGATT[A/G]CAGGCGAACACCACC | 58513 |
rs766479239 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411142 | CGAAAACCTGCAGAC[-/A]AATGTTCCTAGCAAC | 58513 |
rs766499082 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378726 | GGGGAGCCAGGGTCT[C/G]CATCAGCCACAGAAG | 58513 |
rs766509172 | snp | A/C/G | 3.29757e-05 | 0.00406041 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403870 | TGGCTCGGTTCAGAT[A/C/G]GTCTTCCTGGGACTT | 58513 |
rs766578229 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464635 | GTCCTCTTTGCCTCC[A/G]TGTGAAAGGCTATTC | 58513 |
rs766608940 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466561 | AGTGTCCAGCAAAAA[A/G]AAGATGCCAAATAAA | 58513 |
rs766615514 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392356 | GAGGTAAATGGGTCA[C/T]TCTTTGTCTGTTTCT | 58513 |
rs766617787 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404053 | CGCAGACACCTAACC[A/C]AGGCCCGACACCTGG | 58513 |
rs766623455 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388934 | AACCCCAACAACCTA[A/C]ATCAAACACAATGTC | 58513 |
rs766642664 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384711 | TCACTTTTCAACACC[C/G]CTTGAGAGTTCTGTC | 58513 |
rs766671184 | snp | C/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436938 | TCCCGTTCACTTACC[C/G]TCACAGCCCAGTGGG | 58513 |
rs766683768 | in-del | -/AT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425501 | GTAACTTTCCAAGAC[-/AT]GTGTTGAATTATTCC | 58513 |
rs766689784 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395407 | CTGTCTGGAAAGGAT[A/C]CGGATGCAACTCTTG | 58513 |
rs766700835 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463552 | CAAGAACCTGCCATA[C/G]CTCCCTACTGCCTCT | 58513 |
rs766705514 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426975 | GTCCTTGTTTTTAGG[A/C]AATACGCACTGAAGT | 58513 |
rs766718107 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454779 | ATGGACCAGGAAGGT[C/T]GTCAGAACACAGAAT | 58513 |
rs766752894 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418010 | GGACTTGAGGAGGGT[C/T]GATGCCTTTACTGAC | 58513 |
rs766791166 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427010 | GTGGATGAAGAGGCA[C/T]CATGTCTGCAACTTA | 58513 |
rs766808591 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383747 | TCTCAAGTGCTTCTC[A/G]GAATCTGTGTTCTGT | 58513 |
rs766839334 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470120 | GGCGCAGTGGCTAAC[A/G]CCTGTAATCCCAGCA | 58513 |
rs766871790 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458799 | TCACCTCCTTCCCCC[A/G]GCTGGCAGAGCTCTA | 58513 |
rs766887903 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399338 | GGAGAACAGACCCAT[C/T]TGCCAACTTGGGGGA | 58513 |
rs766917614 | snp | A/G | 1.7184e-05 | 0.00293117 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413870 | TAAAAATATTTCATG[A/G]AAACAAGAGTGAATA | 58513 |
rs766925097 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368940 | ACCACTCCAGCAGAG[A/C]TCATCCAAGGCCACT | 58513 |
rs766936780 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358227 | AGGAAAGTTCCTGGT[A/G]CCTTCAGAGTCGACC | 58513 |
rs766977653 | snp | A/G | 1.66123e-05 | 0.00288199 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377128 | CTTACTGACCGCTGG[A/G]CGGTTTAGGCCGTGG | 58513 |
rs767014421 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385515 | GTCTCAATGGGTCAG[A/G]AGGCGAGGAGCAACT | 58513 |
rs767014625 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398279 | ATGGAATGGTTTTTC[C/T]TACCTGGGAAAGAAT | 58513 |
rs767054349 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404313 | CCTGGAACTCCCTGT[A/G]TTGTGGGGCACAGCC | 58513 |
rs767070496 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435160 | TTTCAACATGATGGC[C/T]GGGTTGGTCTTGAAC | 58513 |
rs767090200 | in-del | -/GGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412714 | GGTGCAGCGGGGGGT[-/GGGG]GGGGGGGGGGTGTCA | 58513 |
rs767100134 | snp | A/G | 1.65143e-05 | 0.00287348 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377265 | GGGGGCTGTAAGAGA[A/G]GACATGAAAGAGAGG | 58513 |
rs767108369 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363563 | TGTCCTTGTGGGCTC[C/T]GGGGCTACAGCCCCC | 58513 |
rs767111665 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459281 | AAATGAAATAAGTCC[C/T]TCCTGCCTCCACACT | 58513 |
rs767130838 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417451 | TTCTGAATAAACCTG[C/T]GATGAGCAAACTTCC | 58513 |
rs767137344 | in-del | -/GA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367971 | AATAAACATGAGAGT[-/GA]GAGAGAGAGAGAGTG | 58513 |
rs767148190 | snp | A/T | 1.6513e-05 | 0.00287336 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437740 | ATCTGGTATTAGAAG[A/T]ATGTGAACTTGAAGG | 58513 |
rs767152006 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376689 | CACCCTCACCCCCAA[A/C]AGGCCCTCCCTGAGC | 58513 |
rs767190065 | snp | A/G | 6.61135e-05 | 0.00574912 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385103 | GACACTAGCAGAGGC[A/G]CGGGGGCTCCGTGGA | 58513 |
rs767198544 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413374 | GCTACACCTCAGCCA[A/G]GGGCTGCACTGCCAT | 58513 |
rs767243121 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401111 | TTAGACGATAAAGCT[A/G]ATGATGACGGGCCCG | 58513 |
rs767245218 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412963 | TCCCGCCCATCAAGG[-/A]ATCTGAGATCATTGA | 58513 |
rs767274511 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413174 | CATACTGGCCAAGCT[C/T]TCCATTGTCCCCGTG | 58513 |
rs767283656 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411726 | TATTTTTGAGGCAGG[G/T]TCTCACTCTGTTGCC | 58513 |
rs767315898 | snp | A/G | 0.000180196 | 0.0094903 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425269 | GGACGGGGGCAGGGC[A/G]GAGGGCACGGGCTCC | 58513 |
rs767335209 | in-del | -/GGAGGCCGA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426393 | TAATCTCAGCACTTT[-/GGAGGCCGA]GACGGGCAGATCACC | 58513 |
rs767339697 | in-del | -/CT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359107 | GTGACCTGGGCCCCC[-/CT]GACTGCCAGCATGGA | 58513 |
rs767352689 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455219 | AATTCCTGGGCTTAA[A/G]TGATCCTCCTGCCTT | 58513 |
rs767358291 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456152 | TTGCAGCGAGCCGAG[A/G]TTGTGCCATTGCACT | 58513 |
rs767359234 | snp | A/C | 1.72451e-05 | 0.00293637 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361841 | CTGCAGAGGAGGGGA[A/C]AAATGGGTCTTTTCC | 58513 |
rs767360401 | snp | C/T | 1.68108e-05 | 0.00289916 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425202 | GGCTGGCAGGCAGGA[C/T]GGGGACGGCGCCAGG | 58513 |
rs767367384 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462408 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGGG | 58513 |
rs767374546 | in-del | -/GAG | 5.21544e-05 | 0.00510632 | cds-indel, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361831 | GAAGGTTTAGCTGCA[-/GAG]GAGGGGACAAATGGG | 58513 |
rs767390375 | in-del | -/AC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437712 | CACACATGCACATAC[-/AC]ACACACACACACATC | 58513 |
rs767403220 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374227 | GGGCATGGCCTGGCC[C/T]GTCTCCCTCACGGGT | 58513 |
rs767415485 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371850 | CTGATCTTGATCTCC[A/G]GTCCGTTGCAGAAAA | 58513 |
rs767429709 | snp | A/C | 3.30579e-05 | 0.00406544 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441937 | CTTCTTTAGAAAAAG[A/C]GCAGCTTCACTCGCC | 58513 |
rs767464218 | in-del | -/AC | 4.94462e-05 | 0.00497199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395301 | TAAATTCGACATAAA[-/AC]ACACAGTCTTTCAAT | 58513 |
rs767483752 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378039 | GAATGGATGGTGGGT[A/G]GGCAGATGGATGGAA | 58513 |
rs767488360 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465684 | AAGAGCCTGTCTCTA[A/G]AGGAAAAAGGAAGAC | 58513 |
rs767549945 | snp | A/C | 2.58035e-05 | 0.0035918 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361762 | GGGGTGGCCCGGAGG[A/C]GGAGGACTCAACTTA | 58513 |
rs767571837 | snp | C/T | 3.29614e-05 | 0.00405951 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403751 | GTTGATTTCGTCTTG[C/T]GTTGACTTCAGGGAC | 58513 |
rs767572230 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388607 | CCAAGGCAGGCAGAT[C/T]ACGAGGTCAGAAGAT | 58513 |
rs767594289 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360864 | GGCAGGGCTGTGTTC[A/C]AAGAGCCATCCCAGG | 58513 |
rs767608644 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445587 | CGACAGAACTGAAGA[C/T]ACATGTTGCTAATGA | 58513 |
rs767642118 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419767 | GCCTAGTTATCCCCA[C/T]AGTTCGAGGCCCTGA | 58513 |
rs767655570 | snp | C/T | 1.8183e-05 | 0.00301515 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386217 | AAAGGGATCACTGGA[C/T]TCAAAGGGGTCGAGC | 58513 |
rs767663912 | snp | A/G | 1.65938e-05 | 0.00288039 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418081 | TTGCTTAACTTCCCC[A/G]TTTGCCTCGTATCGG | 58513 |
rs767747279 | snp | A/G | 1.66969e-05 | 0.00288932 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425063 | CTGAGAGGGGGCTGT[A/G]CCCGCTGAGGGCTCC | 58513 |
rs767747929 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401838 | GCAACACCCTGGGGC[A/G]CTGCTTGCCATTACT | 58513 |
rs767752550 | snp | A/C/G | 3.33413e-05 | 0.00408286 | missense, synonymous-codon, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377123 | GAAAGCTTACTGACC[A/C/G]CTGGGCGGTTTAGGC | 58513 |
rs767759863 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398114 | CACCACCCTGGGGCA[A/G]CCAACTTAGGGGTGC | 58513 |
rs767766723 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432072 | TAGGGGCCCTGGAAC[A/C]AATCCCCCTAAGTAT | 58513 |
rs767791695 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468627 | CTGGGATTATAGGCA[A/T]GAGCCACAGCGCCCA | 58513 |
rs767795704 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360134 | CAGGAAATAGAATTA[C/T]GAATTTCAGAAAGAG | 58513 |
rs767805924 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403860 | AGCTCCGACTTGGCT[C/T]GGTTCAGATCGTCTT | 58513 |
rs767826900 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430456 | TGAAGATCTGCTTCG[C/T]CATCTGAAAAATGGG | 58513 |
rs767854691 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382258 | TCCAGAATGCCCGCG[C/T]CATTTCCGAATCCCA | 58513 |
rs767883423 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439003 | CTGTCAGGTGCCTCC[C/T]TCCTAACCCAGGACC | 58513 |
rs767917597 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366774 | ATGACCAGACGCTTT[A/G]AGCAAAGAAAGCCCC | 58513 |
rs767961108 | snp | C/T | 9.8894e-05 | 0.00703116 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434442 | AGAGCAAACCATTGA[C/T]GGGCAAGAGGCTTTC | 58513 |
rs767991057 | in-del | -/T | 1.64768e-05 | 0.00287021 | frameshift-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392366 | GTCATTCTTTGTCTG[-/T]TTTCTTGAAGAAGTC | 58513 |
rs767997047 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417229 | CACGGGCTCTGCCCA[C/T]GACCTGCCTGGGACC | 58513 |
rs767997653 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452349 | TACTCAGGAGGCTGC[A/G]GCAGGAGAATCACTT | 58513 |
rs768028747 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468754 | GCAGTGGCTGACACC[A/G]TAATTCCAATACTTT | 58513 |
rs768048586 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385643 | AGAGTACTGGATACA[C/G]TCGCCTATGATACCA | 58513 |
rs768063466 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393916 | CCAGGACTGGACACA[A/G]TCTAAAGACCGGTCC | 58513 |
rs768093034 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407687 | AAATCAATAAAGCTG[A/T]AATACACAATTGTTT | 58513 |
rs768100097 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429706 | GATGGGGCCCTGTCA[A/C]CTGGCTGCTGCTGAG | 58513 |
rs768109445 | snp | C/T | 1.6736e-05 | 0.0028927 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442015 | AGGCAAAATAACTTT[C/T]CAGCAAATGCAGCAG | 58513 |
rs768122034 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427875 | CTCCAGCCTGGGTGA[C/T]AGAGCAAGACTCCGT | 58513 |
rs768125822 | snp | G/T | 9.51973e-05 | 0.00689852 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425358 | GAAGGGGCAAGGCTG[G/T]GGCCGGGACCATCAG | 58513 |
rs768151103 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394896 | CTTGATGCCTTGGCT[C/T]TCTGGTTAACAGGGT | 58513 |
rs768168169 | snp | A/G | 2.5235e-05 | 0.00355202 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362029 | GAAAGAAAGAAATAT[A/G]AGTTACTCACCCGGA | 58513 |
rs768180477 | snp | C/T | 3.30819e-05 | 0.00406692 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441922 | GTCCGAGAGGCCAGA[C/T]TTCTTTAGAAAAAGC | 58513 |
rs768208405 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443254 | TTGGGGGCAGGATTA[C/T]AGTGTTTATCCAACA | 58513 |
rs768241448 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460159 | GGTGGTGTGCTGAGG[A/T]GCACCTGCAGTCCCA | 58513 |
rs768248048 | in-del | -/AAGA | 1.65589e-05 | 0.00287736 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437005 | TGGTGTCGTGCTGAG[-/AAGA]GAGAGAAACATTCCT | 58513 |
rs768262362 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384582 | TCAGGTCACCGTGTG[A/G]TGAGGGCCGGACACC | 58513 |
rs768287701 | in-del | -/TTTT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450477 | GGCATGTCCATCTTC[-/TTTT]TTTTTTTTTTTTTTT | 58513 |
rs768290801 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472910 | AACCCGGGAGGTGGA[A/G]GTTGCGGTGAGCCAA | 58513 |
rs768304959 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359681 | GACTGGGTAGTAAAG[C/T]GAGACCTTGTCTCTA | 58513 |
rs768331449 | snp | A/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392332 | GAAGGGTTTTTCGTG[A/T]ATGGATCCGAGGTAA | 58513 |
rs768399854 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449876 | CTCTCCAGAGAATTA[C/T]GCTGAATGACAAAGG | 58513 |
rs768404054 | snp | C/T | 3.31268e-05 | 0.00406968 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418077 | GTCTTTGCTTAACTT[C/T]CCCGTTTGCCTCGTA | 58513 |
rs768413844 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369854 | CTTTGACATACCCTG[C/T]GTGAACACCCCTGGG | 58513 |
rs768416625 | snp | C/T | 3.3012e-05 | 0.00406262 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436978 | AGGGCGGTGTGACCA[C/T]CAGAGGGCTGCTGGT | 58513 |
rs768417176 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471424 | TGCGCCCGGTGCAGG[C/G]GTGGCGGAAGCAGCT | 58513 |
rs768418616 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365990 | GAGAAGGGAATAAAG[A/G]CATCTGCCCTTCCTG | 58513 |
rs768419431 | snp | C/G | 1.73736e-05 | 0.00294729 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361831 | GAAGGTTTAGCTGCA[C/G]AGGAGGGGACAAATG | 58513 |
rs768424349 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403842 | TCCTGCTGCAATCGG[C/T]TCAGCTCCGACTTGG | 58513 |
rs768437608 | snp | C/G/T | 3.33925e-05 | 0.00408599 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361898 | TACTTTGGAACGGGT[C/G/T]GCCGCTGTCAGCCCC | 58513 |
rs768441586 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445630 | CCCCAGGCAGTCTGT[-/G]CACTGGCCCCTGTGC | 58513 |
rs768453932 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411127 | AAACAGGTGTTCGCA[C/T]GAAAACCTGCAGACA | 58513 |
rs768504597 | snp | C/T | 5.26505e-05 | 0.00513054 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437057 | TAAATCATAGGTGGG[C/T]GGGTTTGCTGAAAAG | 58513 |
rs768554990 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435959 | TATAAGATCTCTTGG[C/T]ACTGTTTCCCATGAC | 58513 |
rs768583517 | snp | C/G | 1.75243e-05 | 0.00296004 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418149 | CATCACAGGCGCCGA[C/G]TCAGCCTGAACCCAA | 58513 |
rs768601317 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431864 | AAACGCAAAATAAAG[C/G]AAAACACGGTTGACT | 58513 |
rs768641776 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467949 | AGCCTCCTAGAATGG[A/T]GGCACCTACTGAAAT | 58513 |
rs768673554 | snp | A/G | 1.67022e-05 | 0.00288978 | stop-gained, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403912 | CCTGAGATTGGATTT[A/G]CGTTTTCAGTGATGA | 58513 |
rs768680862 | snp | G/T | 3.1873e-05 | 0.00399193 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361747 | CAAGCGGAAGGGAGT[G/T]GGGTGGCCCGGAGGC | 58513 |
rs768763664 | snp | A/G | 1.64999e-05 | 0.00287222 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395484 | TACAATTTTGTGAAG[A/G]AACAGGACAGGGATT | 58513 |
rs768765870 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381102 | GCACAGATGACCCCA[C/T]CAGATCCCTTCCCTG | 58513 |
rs768769469 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401654 | CCACCTAAGGAAAAG[A/G]TCACACCTGTCTTGG | 58513 |
rs768784054 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412625 | AGACCCCATCTCTAT[C/T]TGGAAAAATATATAT | 58513 |
rs768899381 | snp | C/G | 1.70243e-05 | 0.00291751 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404792 | GAGGATGGGAAAAAT[C/G]AAGCATGTCCAAGAT | 58513 |
rs768910666 | snp | G/T | 1.64795e-05 | 0.00287045 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395325 | CTTTCAATGAGAAAG[G/T]GGGTAGCAAGTGAGA | 58513 |
rs768952454 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382000 | TTCTACCCTCTGTGT[C/T]GCGCAATAGGACCCG | 58513 |
rs768966910 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464183 | CACAGGCAGTGCAGA[C/T]GGAAATCCGAGACAA | 58513 |
rs768974096 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440914 | AAGTCCCATATCTGC[A/G]GAAACACAAAAATGC | 58513 |
rs768982241 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361707 | GGTTTGCCTTTAAAA[A/G]GAGACAAAAATCCCA | 58513 |
rs768994840 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388359 | AACTTATCAAATTTG[G/T]TGAAAAGCATAATTT | 58513 |
rs769003506 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396222 | ATGTGACTAACAGGA[A/G]GAACTGGGTGTGGGA | 58513 |
rs769010780 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420466 | GACCCACTGTCCCTA[C/G]CCAGTTGGAGGCGGC | 58513 |
rs769014098 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373167 | ACTGGACAGCCTATG[A/G]GTCCTTCAGACTTTT | 58513 |
rs769024320 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463007 | ATTTTCTGTGTGCCT[C/G]GGTGCCCAGCTGCAG | 58513 |
rs769048116 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402712 | ACCTATATTTTTGGG[A/C]AACAAACCAAGACCC | 58513 |
rs769061558 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389929 | GGCCAATAGACAGAA[C/T]TCAAAAAAACATTCA | 58513 |
rs769101195 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374370 | ACAAAGATGCAGTGG[C/T]CTGTGCCACGAGTAA | 58513 |
rs769103871 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369922 | ATGCTATCTATGCAT[A/G]AGCCAGGCACGGGGA | 58513 |
rs769110686 | snp | A/C/G | 8.25629e-05 | 0.00642463 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403718 | ATGTGGCAGGGACCC[A/C/G]ACTCCGTGAAGTACC | 58513 |
rs769119140 | snp | A/G | 1.65002e-05 | 0.00287225 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440817 | TCACCCAGCCTGGGG[A/G]CTCTGCCCAGCCCCT | 58513 |
rs769121354 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426659 | CAGAACAACGACAAC[A/G]AAAAAACAAAAAGTC | 58513 |
rs769125123 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464032 | AAACACGGGGAGCAG[A/G]TGTGCTGTCAGCTGC | 58513 |
rs769168456 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464422 | CCACCAGCCACTGGC[C/T]ACTCTCTCGGCAAGC | 58513 |
rs769168589 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357396 | AGGATGAAGCGTGGG[A/G]TGGGATAAGCCAGAC | 58513 |
rs769170580 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402579 | CAGGGTCTCACTCTG[C/T]CACCCAGACTGGAAT | 58513 |
rs769205688 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435422 | TGAGTGAGGCAGTGG[C/T]TTCCAGTCTGTTCCA | 58513 |
rs769213716 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433060 | AAGTAATCTGCCCGC[C/T]CCAGCCTCCCAAAGT | 58513 |
rs769222021 | snp | A/C | 1.67922e-05 | 0.00289755 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421528 | CTTTTTATGACCCCC[A/C]GACACATGCTTTTTG | 58513 |
rs769238150 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409376 | CCTACATGGAAAAGC[A/G]AAAACTATAAAACTC | 58513 |
rs769246265 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440493 | CTGTGCTGTGGTTAT[A/G]TAAGACACCATCACT | 58513 |
rs769252960 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446296 | CCAACTCTGATCCCC[A/G]CACGTGGCCGAGGGC | 58513 |
rs769266877 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431871 | AAATAAAGCAAAACA[C/T]GGTTGACTCTTGAAC | 58513 |
rs769290100 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398760 | AGTTTTGACCTGCTC[C/T]GCTTCTGACCAGGGC | 58513 |
rs769313883 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404691 | TCTTGAGCATCCTGT[C/T]TCTGAGCCTCGAGCT | 58513 |
rs769353384 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440946 | CATAAGCATGACTGC[C/T]GATCACTGTCCACGT | 58513 |
rs769369841 | snp | C/T | 1.66175e-05 | 0.00288244 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441906 | CCTTCCCAAGGATAA[C/T]GTCCGAGAGGCCAGA | 58513 |
rs769414574 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453080 | GCTGGGATTACAGGT[A/G]TGAGCCACCGCGCCC | 58513 |
rs769416686 | in-del | -/C | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383141 | ATGGAACGCTGGAAT[-/C]CAAAACAAGATAGTA | 58513 |
rs769426091 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448502 | ACCATTGCACCATTG[C/T]ACTCCAGCCTGGGCA | 58513 |
rs769446500 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376366 | TCTGGCCAACTGGCC[A/G]CCGGCCTAACTCTGT | 58513 |
rs769457784 | snp | C/T | 5.45499e-05 | 0.00522226 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425250 | TCTTGGAGGGTGGGA[C/T]GAGGGACGGGGGCAG | 58513 |
rs769479119 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460025 | TCAGGCCTGTAATCC[C/T]AACACTTTGGAGATT | 58513 |
rs769519318 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408307 | CAGCTGGCTTCTTTG[C/T]AGAAACAGACAAGCT | 58513 |
rs769530395 | snp | A/G | 4.94605e-05 | 0.0049727 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395293 | AACCACTCTAAATTC[A/G]ACATAAAACACACAG | 58513 |
rs769552082 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356460 | GGGATTACAGGCATG[C/T]GCTACCATGCCCAGC | 58513 |
rs769578542 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392312 | CACTCACCTTCGAAG[A/G]TAAGGAAGGGTTTTT | 58513 |
rs769586329 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379262 | GTGAGCTGAGATCCC[A/G]CCACAGCAGCACTCC | 58513 |
rs769607330 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363285 | AACTCTGGAAGTTTC[A/G]AAGCTAATGTTTAGA | 58513 |
rs769628478 | snp | C/T | 1.78261e-05 | 0.00298542 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361995 | TTTACCTGGAAAGTT[C/T]AGGAGAAAAAAAAAA | 58513 |
rs769636042 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447895 | GTATTGGCAGGGGGC[A/G]GGCACAGACAGTAAT | 58513 |
rs769676563 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450281 | ACCTTGATTCCGTGC[C/T]CTGATGCCCTCCCCA | 58513 |
rs769678123 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454990 | AAAATTAGCCAGGTG[-/T]TGGTGGCGCACACCT | 58513 |
rs769679301 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385350 | GACACGTGTGTCTGC[A/C]TGAAGGCCTCTCAGC | 58513 |
rs769702902 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404811 | CATGTCCAAGATAAC[A/G]GGGGGCAGCCTGGGC | 58513 |
rs769725417 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467462 | GCCTGGAAAGTTGTT[C/T]TAAAGTTCAGAATGG | 58513 |
rs769757919 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459162 | GAGCACTGTCACATA[C/T]GCAGTCCATCATGGT | 58513 |
rs769769095 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409867 | CACTTGAACCTGGGA[A/G]GCGGAGGTTGCAGTG | 58513 |
rs769794342 | snp | C/T | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418065 | TAACGCGAATTGGTC[C/T]TTGCTTAACTTCCCC | 58513 |
rs769807744 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423701 | TCAAGTCTGGTGGAC[A/G]TAAAGATGCCAATAA | 58513 |
rs769844818 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472807 | GTGAAACCCCATCTC[C/T]ACTAAAAAAAATACA | 58513 |
rs769855342 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469869 | TTTGGAATTATACCC[G/T]TGGTTCCCCCAGAGT | 58513 |
rs769856009 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411355 | CTTTTGGGTTAATGG[A/T]AAGTTAGTGTCAAAC | 58513 |
rs769856270 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380222 | CTAGTCACACCAAAG[C/T]GGCCATCTAAGGCTC | 58513 |
rs769877809 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416246 | CCATTTTCAGCCAAG[C/T]AAACAATCTCTTTCC | 58513 |
rs769881864 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403729 | ACCCGACTCCGTGAA[A/G]TACCTGGTTGATTTC | 58513 |
rs769908231 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458931 | ATTTCATCGTCGTGA[A/G]GACATCCTGGAGTGA | 58513 |
rs769915493 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392001 | TAGAGTTGAGGGGTA[A/G]GAATGGGGATAGAGA | 58513 |
rs769930275 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436797 | GCCACTCACACTGAG[A/T]CAGAAGAGCTGACAC | 58513 |
rs769942401 | snp | A/G | 1.68371e-05 | 0.00290143 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404779 | CAGGGGTTTACGTGA[A/G]GATGGGAAAAATGAA | 58513 |
rs769955238 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455770 | GGGACTTGTCAATCA[A/C]CGGCTGTTGTGATTC | 58513 |
rs769971905 | snp | A/G | 1.65124e-05 | 0.00287331 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440797 | TGTGGAAGGAGCCGT[A/G]GAGGTCACCCAGCCT | 58513 |
rs769973586 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421391 | TCCTGGCCACTCACG[C/T]AGCCATCCAGGTCCA | 58513 |
rs769982777 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435752 | AAACACTTGGCACTT[C/T]GGGCTTGTTCTTTCT | 58513 |
rs770000878 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404669 | CTGGTCCATCTCGTC[C/T]AGGCGGTCTTGAGCA | 58513 |
rs770022430 | in-del | -/CTT | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473205 | AGGAAAAGAGAAGTC[-/CTT]CTAGGTACTTCAAAC | 58513 |
rs770066852 | snp | G/T | 1.67105e-05 | 0.0028905 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421517 | TAATCTGGAAGCTTT[G/T]TATGACCCCCAGACA | 58513 |
rs770090625 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393947 | GGGAAACACTGAATT[C/T]TACCTGTTGAAGTTG | 58513 |
rs770106913 | snp | A/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401582 | GAAATGGGAAACTAC[A/T]TGTCCCCAGGTTCGA | 58513 |
rs770112691 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430373 | CTGCCCCGCCCTGTC[C/T]ACAGTAGGACCTCAT | 58513 |
rs770129522 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431739 | CAGTGTTTGAGGTGA[C/T]GGATATGCTAATTAC | 58513 |
rs770146346 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405900 | ACAACGGGCATTGTG[A/G]CAAGCCTCCTCCCTC | 58513 |
rs770163430 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360635 | GCCTGTCGTCCCAGC[C/T]ACTCAGGAGGCCAAG | 58513 |
rs770184097 | snp | A/C/T | 3.29898e-05 | 0.00406128 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402374 | CTTCGCTCAGGTTGG[A/C/T]CAGGTCGGTCAGGCT | 58513 |
rs770189310 | in-del | -/CAAATACCA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417468 | TGAGCAAACTTCCAG[-/CAAATACCA]GTGAGCCTCTGATAT | 58513 |
rs770189347 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387838 | AAAGAGTAAGTGAAG[C/T]TGAAAACAGAGCAGT | 58513 |
rs770191209 | snp | C/T | 0.000125006 | 0.00790488 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402534 | GGTCAGGAAAACATG[C/T]CAGAAAAGACGCTTT | 58513 |
rs770207069 | snp | A/C | 9.89332e-05 | 0.00703255 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385173 | CTTCAGCACTATTGA[A/C]GGACCCACTTCCGAA | 58513 |
rs770246482 | in-del | -/GGAA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428415 | AGAAAAGGGAGGGAG[-/GGAA]GGAAGGAAGGAAGGA | 58513 |
rs770261998 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381728 | TAGCTTTAAAATGGG[A/C]CGTTTAGGGTCGGCT | 58513 |
rs770275349 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387168 | AAATAGAAAATATAC[A/G]AAAGAAACAAATGAA | 58513 |
rs770275949 | snp | A/G | 1.67761e-05 | 0.00289617 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402469 | CTTTCATGCAGCTGG[A/G]AAAGTTTGCTCCTTG | 58513 |
rs770277155 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415198 | CCTGTGAGGACACGG[-/C]AAGAAGGTGACTCTC | 58513 |
rs770301103 | snp | A/G | 1.73522e-05 | 0.00294547 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377085 | CCGCCATCCGGCACC[A/G]GTAGGCGGTGGCTGC | 58513 |
rs770321187 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367294 | ATGAAATTAAAGACC[C/G]TCTTGGGTGTGCTGA | 58513 |
rs770337165 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373357 | CACTGTGTGCTGGCC[A/G]TGTGGTCTCCCTGAG | 58513 |
rs770339659 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375321 | GTGTCTGCAGGCGTG[A/G]AGGATGTGTGTACAC | 58513 |
rs770343181 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371507 | GCTCATCACCATCAC[C/T]TATGCGGCTTTGTTT | 58513 |
rs770353852 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451687 | GTGCCCGCCACCTCA[C/G]TCGTCTAATTTTTTG | 58513 |
rs770383778 | snp | A/C | 4.95585e-05 | 0.00497763 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437839 | ACTCTGTGCACAGGC[A/C]ACCAGTCTCAGTGCA | 58513 |
rs770388877 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420241 | TTGATCCAGGTGGAT[G/T]AGTGATTTCCTGTGT | 58513 |
rs770396488 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467200 | TGCCCAGGCTGGAGT[A/G]TGCAGTGGAGTGATC | 58513 |
rs770403995 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456720 | TCAGGAAGGGCAGGC[A/G]GGACAAAGTCAGCCC | 58513 |
rs770426146 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452947 | GACTACAGGTGCCCA[C/T]CACCATGCCCAGCTA | 58513 |
rs770437894 | in-del | -/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405671 | GTGCTTTGCCTTACA[-/GT]GGGACATGAGCACAC | 58513 |
rs770465808 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407046 | CGCTGAATCTGCAGG[C/T]CCCTTGATCTTGGAC | 58513 |
rs770476552 | snp | A/C/T | 3.30089e-05 | 0.00406246 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403723 | GCAGGGACCCGACTC[A/C/T]GTGAAGTACCTGGTT | 58513 |
rs770476724 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462697 | TAAAACAAAGAATCA[A/G]GGAAGTGGGACTCTG | 58513 |
rs770484350 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465628 | TCGAGGCTGCAATGA[A/G]CTTTGATTGCACCAC | 58513 |
rs770490994 | snp | A/T | 1.87689e-05 | 0.00306335 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386149 | GGAATAGTCAGGAAG[A/T]AAAATAAGTCATGGG | 58513 |
rs770570774 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416152 | GGAGCTGATAGAATA[C/T]TGCACCTGTTAATAT | 58513 |
rs770573041 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373852 | TGTTAGAGGTTAGTA[C/T]GGAATCACAGCACAA | 58513 |
rs770597381 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384344 | AAGCACAATGGTGCC[A/G]CAGCCCTGTCCTTCC | 58513 |
rs770646246 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470756 | CAACTCTCTTTGGGT[A/T]TGGAATTCTTAATTG | 58513 |
rs770693426 | snp | C/T | 0.000247372 | 0.0111187 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16471913 | CCGCCCGGCCCGTAC[C/T]TGCTGGGAGAGGGGG | 58513 |
rs770718835 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388215 | GCCTGGCTAATTTTT[C/G]TATTAGTAGAGACGG | 58513 |
rs770729430 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458229 | GTGACAGCGTCAGCC[C/T]CCTAGTGCACTGTTC | 58513 |
rs770760239 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404662 | CCTTCTGCTGGTCCA[C/T]CTCGTCCAGGCGGTC | 58513 |
rs770809136 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398608 | ACCTGGATAAAGCAG[C/T]GAGTTAAGAATGCCA | 58513 |
rs770842633 | in-del | -/GA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365540 | TCTGCTGTTTAGGCT[-/GA]GATAGAGCAAGTGTG | 58513 |
rs770848529 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435656 | GCTGCAGGTCTTTCT[C/T]GGGGGCCTGGGATCC | 58513 |
rs770907460 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384435 | GTAAGGGGCTTCTAT[C/T]GTTGTTTTTTGACTT | 58513 |
rs770968446 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440173 | CGTGGTGGCTCATGC[C/T]CATAATCCCAGCAGT | 58513 |
rs770970114 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425849 | CAGTGGAACTGAGGA[C/T]GCATCCATGAGGCAG | 58513 |
rs770975995 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421742 | GCTCTCCTTGTCCAT[C/T]CACCCTGCCACCCAG | 58513 |
rs770981299 | snp | C/T | 3.46296e-05 | 0.00416096 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421274 | CTTCACCCACAGGCC[C/T]CCTGGAGCCACCCAC | 58513 |
rs771009099 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372126 | GTGGTCCCCAGAGTG[C/T]ACTTTCTGGCTTAGA | 58513 |
rs771052369 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390283 | GGGAATCTTTTATAA[C/T]GATAAAAAGGTTGTT | 58513 |
rs771067071 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448369 | AACCCCATCTCTACT[A/G]AAAATGTAAAATTAG | 58513 |
rs771110967 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437814 | GATTGCTCAAGGTAA[C/T]TTCATGGCCACTCTG | 58513 |
rs771112364 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375403 | ATAAAAATACATGGC[C/T]GCACGTGGGAATGTG | 58513 |
rs771125223 | snp | A/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421384 | CTTCACCTCCTGGCC[A/T]CTCACGTAGCCATCC | 58513 |
rs771127000 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460763 | AACGTTTGCAAGAAC[A/G]TGCGCCTAGGCCAAT | 58513 |
rs771173287 | snp | C/T | 0.000247829 | 0.0111289 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404578 | TGCCCCGGAGGTGGC[C/T]GGGACCCACCATCTG | 58513 |
rs771187081 | snp | A/C | 3.30732e-05 | 0.00406638 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385083 | ACCATGACAAGAGGC[A/C]CAAAGACACTAGCAG | 58513 |
rs771215955 | in-del | -/G | 5.24494e-05 | 0.00512074 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428801 | TAACTGTGGGAGGAA[-/G]GACTGGGTGAGAGTG | 58513 |
rs771218910 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417040 | AGACCCAATTGCCCT[A/G]GCTGTCAAGGATAAC | 58513 |
rs771225621 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365394 | TTCACTGAAAGAACT[C/T]AGGACACAGATCTAC | 58513 |
rs771280577 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443353 | TTATAGTCATTGGAT[A/T]TGAACCAATACGCAC | 58513 |
rs771280676 | snp | A/G | 1.77338e-05 | 0.00297768 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361817 | AGGCAGAGGCCTTAG[A/G]AGGTTTAGCTGCAGA | 58513 |
rs771300986 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371463 | AAGCTGTTCGTTAGT[A/G]CAACTGTGGGGAGGG | 58513 |
rs771309306 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391204 | CCAAATAAATAGGAG[A/T]AAGGAAATGGAAAAA | 58513 |
rs771332123 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363314 | GAAAAAACCAGGAAC[C/T]GCCTGTCCCTCCAGG | 58513 |
rs771332852 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454456 | GCTTCCTATGTTCCC[C/T]GGTGTACTATGTCAG | 58513 |
rs771335567 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455568 | ATCTACACCTATGGG[C/T]TGTGTTCTCCCATCT | 58513 |
rs771355456 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408657 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs771374210 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402363 | CAGGGAGACGCCTTC[A/G]CTCAGGTTGGCCAGG | 58513 |
rs771405804 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400262 | GAATCACTTGGACCC[A/G]GGAGGCAGAGGTTGC | 58513 |
rs771407453 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412367 | TAGCCAGGCATGGTG[A/G]TGCGTGCCTGTAATC | 58513 |
rs771410283 | in-del | -/A | 8.26918e-05 | 0.00642955 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377287 | AAGAGAGGCAAAAAT[-/A]AGTTGTTAAAACAAA | 58513 |
rs771414163 | snp | C/T | 1.67161e-05 | 0.00289098 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417525 | TGTAACATCTGGATG[C/T]GGAGGGAAGGGCCGT | 58513 |
rs771423622 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438876 | GTTGGTCAGAAACTC[-/A]TATCTGTGGTTCACC | 58513 |
rs771425073 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406175 | TCCCCTCTCCTCACT[A/G]TGGGGACAAAAACAT | 58513 |
rs771438771 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380146 | ATCTAGTCGCACAGA[C/T]GCAGCCATCTAAGGC | 58513 |
rs771455497 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377699 | CCCACTGAGCTGGCC[A/G]GTGTGGTCACTGCCT | 58513 |
rs771458751 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411213 | CCCCGATGGGAGGAA[C/T]AGATGAAGGAAATGT | 58513 |
rs771552756 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466146 | GGCATGTGCCACCAC[A/G]CCTGGCTAATTTTTG | 58513 |
rs771560358 | snp | C/G | 1.66754e-05 | 0.00288746 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361903 | TGGAACGGGTCGCCG[C/G]TGTCAGCCCCGAGTG | 58513 |
rs771570141 | snp | C/T | 0.000139235 | 0.00834254 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417899 | CCACCTGGTGGCAGG[C/T]GGTGGGAAGGGATGT | 58513 |
rs771589538 | in-del | -/GT | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472406 | TCCTAGGATCGCAGT[-/GT]GTGTGTGTGTGTGTG | 58513 |
rs771590496 | snp | C/G | 1.68932e-05 | 0.00290625 | missense, synonymous-codon, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361970 | AACCAAGCTGGCTTA[C/G]AGGTGTACTTTTACC | 58513 |
rs771633092 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418217 | AAAACAACGGCAGGG[C/T]GTGGTGGCAAGCCCC | 58513 |
rs771683608 | snp | A/G | 0.000277469 | 0.0117753 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442267 | TGAACACAACCCCTT[A/G]GGGAAAAAAAGGGTT | 58513 |
rs771688191 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430131 | ATGCCCAGACTTCTA[C/T]CAGAGTCCCCCTCAC | 58513 |
rs771694946 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425745 | AGGAGATGGAGGCTG[C/G]AGTGAGCTGTGATCG | 58513 |
rs771719536 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457045 | GCAAGGAGCAGGGCT[A/G]GAAGGAAGTGATCAG | 58513 |
rs771745548 | snp | C/T | 1.69166e-05 | 0.00290827 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402485 | AAAGTTTGCTCCTTG[C/T]CTGTGCAACAAAGAC | 58513 |
rs771756204 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397341 | GTAATCCACCCCCCT[C/T]GGCCTCCCAAAGTGC | 58513 |
rs771771403 | snp | G/T | 4.83606e-05 | 0.00491711 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428784 | GGAGAGACCAGCATG[G/T]GTAACTGTGGGAGGA | 58513 |
rs771783338 | snp | A/G | 1.66613e-05 | 0.00288623 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417958 | CTCACCGGGCCGGGC[A/G]TGCCTCTCTCCGAAG | 58513 |
rs771795386 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473089 | CAACCTTGGCCCAAA[C/T]TCTCTACTTATATTA | 58513 |
rs771800151 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378056 | GCAGATGGATGGAAT[A/G]GTAGTTGGATGAATG | 58513 |
rs771812932 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469401 | GACGGAGGGGCCACC[A/G]GTAACCTCGGGGAGT | 58513 |
rs771837110 | in-del | -/G | 1.65499e-05 | 0.00287657 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440768 | TGCCTAGTAATACTT[-/G]GACAGTGGAGGAATG | 58513 |
rs771888913 | snp | A/C | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392340 | TTTCGTGAATGGATC[A/C]GAGGTAAATGGGTCA | 58513 |
rs771890806 | snp | C/T | 1.65105e-05 | 0.00287315 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421350 | GGTTCTGGGTGAGGC[C/T]CGAGTGCATGAAGAT | 58513 |
rs771929203 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367000 | CTGCCTCCAGGCCCT[A/G]AAGCAAAAGCTGCCA | 58513 |
rs771980383 | snp | A/G | 3.30666e-05 | 0.00406598 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404573 | GGCGCTGCCCCGGAG[A/G]TGGCCGGGACCCACC | 58513 |
rs771999579 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447410 | AAGAGAGAGGCAATT[C/G]AGAAAGAAGAGATGC | 58513 |
rs772047392 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438600 | AGTGGCGCAATCACA[A/G]CTCACTGCAACCTCA | 58513 |
rs772050964 | snp | C/G/T | 4.96416e-05 | 0.00498184 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392431 | TTGAAAGGGTCCCCT[C/G/T]CAAATGGATCTAGAA | 58513 |
rs772090450 | snp | C/G | 1.65337e-05 | 0.00287517 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442133 | ACTGTGCTTTCAGCT[C/G]AGGCATGCTCTAGTT | 58513 |
rs772097688 | snp | G/T | 1.65241e-05 | 0.00287433 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436991 | CATCAGAGGGCTGCT[G/T]GTGTCGTGCTGAGAA | 58513 |
rs772100387 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437279 | ACATGTCCAGAGAGA[C/T]GAATGGATAAAGATG | 58513 |
rs772125412 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403587 | GAGTCCTTGGCCCTG[C/T]GCCTCCAGGCCAGCA | 58513 |
rs772167739 | snp | A/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472331 | CCAGTGCGCCTGGGG[A/T]GGCGGTCGCCCACCC | 58513 |
rs772174388 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376330 | TCTGCCACTTGAAGC[-/A]AATAGCTTTCTGTTT | 58513 |
rs772176911 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402871 | ATGACAGGTGTAAGG[A/C]ACTGCACTGCGCAAA | 58513 |
rs772180676 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467458 | CCCGGCCTGGAAAGT[G/T]GTTTTAAAGTTCAGA | 58513 |
rs772192280 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412334 | GTGAAACCCCATCTC[C/T]ACTAAAATACAAAAA | 58513 |
rs772205722 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414784 | GCACGATCATAGCTC[A/G]CTGCATCCTTGACTT | 58513 |
rs772257260 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446314 | CGTGGCCGAGGGCAG[A/G]ACGCCTCCTACATCT | 58513 |
rs772258291 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457764 | GACATCACCCCTCCC[A/G]GGCATCTCAGAGAAC | 58513 |
rs772273887 | snp | C/T | 1.78229e-05 | 0.00298515 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437062 | CATAGGTGGGTGGGT[C/T]TGCTGAAAAGGATAC | 58513 |
rs772327375 | snp | A/G | 1.65151e-05 | 0.00287355 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395495 | GAAGAAACAGGACAG[A/G]GATTTTATTATTTCT | 58513 |
rs772357678 | snp | A/C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426396 | TCTCAGCACTTTGGA[A/C/G]GCCGAGACGGGCAGA | 58513 |
rs772369025 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454364 | ACACGGTATCCTATC[A/G]CCCCGCTACTGGAAC | 58513 |
rs772371052 | snp | C/T | 0.000178619 | 0.00944869 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355695 | TGTCCCGCCTACACA[C/T]GGCCCTCGCCTAGGC | 58513 |
rs772386490 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374590 | CAGAGGGAGACACGA[C/T]GGGAGGTGATAACTG | 58513 |
rs772413802 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379529 | GGGAAAAGGTCTACC[A/G]CCACGTCCAGCAGAC | 58513 |
rs772418301 | snp | A/C/T | 4.94493e-05 | 0.00497219 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377201 | ACTTTTAAAGGGGTC[A/C/T]TCTGAGAATCCTGCC | 58513 |
rs772418516 | snp | C/T | 3.30682e-05 | 0.00406608 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402356 | TCTCTGCCAGGGAGA[C/T]GCCTTCGCTCAGGTT | 58513 |
rs772427510 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453374 | CCTCCCACGGTGCTG[A/G]GATTATAGGTGTGAG | 58513 |
rs772431004 | snp | C/G | 2.02198e-05 | 0.00317954 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386256 | AGGAGAGAGGAAAGA[C/G]TAAAAAGCAGTTCGT | 58513 |
rs772432771 | snp | A/C | 1.65597e-05 | 0.00287743 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377301 | ATAGTTGTTAAAACA[A/C]AGGTGACGGATGTCC | 58513 |
rs772440851 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373098 | AAGCTTGTTCCTTCA[C/T]TGTGATTTCCATGAG | 58513 |
rs772440995 | snp | A/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382739 | GTGAGCTTATGTCAC[A/T]TAGGCTTGATACTGT | 58513 |
rs772444580 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464498 | TCACGTCTTATTTAC[C/T]AAAAGACCTTCCTCC | 58513 |
rs772456124 | in-del | -/ACTC | 2.72305e-05 | 0.00368979 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362034 | AAAGAAATATGAGTT[-/ACTC]ACCCGGACAGAGCAG | 58513 |
rs772489776 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464907 | AACCAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 58513 |
rs772494063 | in-del | -/AGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395851 | TTGGGAGGCTGAGGC[-/AGG]AGAACTGCTTGAACC | 58513 |
rs772494734 | snp | A/G | 1.66693e-05 | 0.00288693 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441901 | ACATACCTTCCCAAG[A/G]ATAATGTCCGAGAGG | 58513 |
rs772522952 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391534 | CTCTGAGCAGGCCCC[A/G]GGCCTGGGTTGCAGC | 58513 |
rs772533372 | snp | C/G/T | 0.000143053 | 0.00845627 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361756 | GGGAGTGGGGTGGCC[C/G/T]GGAGGCGGAGGACTC | 58513 |
rs772544488 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16461077 | TTGGGAGGCCGAGGC[A/G]GGCGGATCATGAGGT | 58513 |
rs772565766 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394460 | GATTCGCCTCTCAGA[A/C]CCGGCAGGCTTCAAA | 58513 |
rs772572896 | snp | C/G | 3.33289e-05 | 0.00408207 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361912 | TCGCCGCTGTCAGCC[C/G]CGAGTGGCTGGAATG | 58513 |
rs772587235 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417592 | TGATGTCATCAAGCT[C/T]CTTCACGCCAGTAAA | 58513 |
rs772592912 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420275 | TTCCATGTCATTACA[C/T]CATGTGTCAATTGCA | 58513 |
rs772605278 | snp | A/G | 3.29843e-05 | 0.00406092 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402381 | CAGGTTGGCCAGGTC[A/G]GTCAGGCTGGCACCA | 58513 |
rs772630296 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421570 | ATTAAAGCACTTCCA[C/T]GCACATTTGGCATCA | 58513 |
rs772656045 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407022 | ACCAGGAAGTGGGTC[C/T]TCACCAGACGCTGAA | 58513 |
rs772659148 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435072 | CTCAGCACTCGTACC[-/T]TCCCGAGTAGCTGGG | 58513 |
rs772666756 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364835 | CCCTCCCGTCCCTAG[A/C]AGCCTCATCTCCCTA | 58513 |
rs772708826 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438239 | GTGCCTGAAATCCCA[C/G]CTACTTGGGAGGCTG | 58513 |
rs772713195 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419375 | GAGGCACGAGAATCA[A/C]TTGAACCCAGGAGGC | 58513 |
rs772730725 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420664 | GCAATTCTTTCCTTT[C/T]GATAGCTCCCAAGTG | 58513 |
rs772736647 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395352 | GAGATACCTTTGAAG[A/G]GGTCAGCTCCTTTAA | 58513 |
rs772750821 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399789 | AGCCTCCCAAAGGAC[G/T]GGGATTACAGGTGTG | 58513 |
rs772751384 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16373620 | CATCTGCTGACCGCT[A/C]TTGCCCATAACCAGA | 58513 |
rs772803912 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460282 | GAGCCTGTCTCTAAA[A/T]ATAAAAAAAGAACAG | 58513 |
rs772822422 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449948 | ACATCATTAAAATGA[C/T]AAAATTGTAGAAATG | 58513 |
rs772837904 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418347 | CCCAAGCCCCTGACC[C/T]GGGCTGAGGAGCCGA | 58513 |
rs772839218 | snp | G/T | 2.61161e-05 | 0.0036135 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428797 | TGGGTAACTGTGGGA[G/T]GAAGGACTGGGTGAG | 58513 |
rs772874348 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460915 | TCATCAAGTTTTTTC[A/G]TGTTTCATCTTTCCC | 58513 |
rs772888933 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430206 | CAGCTGCCCTGCTCC[C/T]CGTGCTCGAGTGGGT | 58513 |
rs772909699 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413194 | TTGTCCCCGTGTGCA[C/G]AGGCTACTGGGGGAA | 58513 |
rs772930096 | in-del | -/GCT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364765 | ACTGGAGCAGAAGGG[-/GCT]GCTCCCTAGGGCTCC | 58513 |
rs772937822 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449138 | AACTAGCCAGGCGTC[A/G]TGGTGCACACCTGTA | 58513 |
rs772957565 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457068 | GTGATCAGAGAGAGA[C/T]TGCCATGGCCCTCCA | 58513 |
rs772957758 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469485 | GAAGAGAGCTGAGCA[A/G]GGGGACAGGGAGACA | 58513 |
rs772972472 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387142 | TGAAAACACAGGTGA[C/T]CTTAGAAGAGAAATA | 58513 |
rs772981587 | snp | G/T | 3.50079e-05 | 0.00418362 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437884 | CAAGTCCAAAGAAAG[G/T]GAAGGAGTAAACAGC | 58513 |
rs772984184 | snp | A/C | 1.85727e-05 | 0.00304729 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403939 | ATGAGATCTGAAATG[A/C]GATGTTAAAAGATGT | 58513 |
rs772989043 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396358 | CCTTGACCATCTGGG[C/T]TCAAGTGATCCTCCC | 58513 |
rs773000630 | snp | A/G | 1.6528e-05 | 0.00287467 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404575 | CGCTGCCCCGGAGGT[A/G]GCCGGGACCCACCAT | 58513 |
rs773052781 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367016 | AAGCAAAAGCTGCCA[A/C]GCGCACCCACGCCAG | 58513 |
rs773070641 | snp | A/G | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441938 | TTCTTTAGAAAAAGC[A/G]CAGCTTCACTCGCCC | 58513 |
rs773084052 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468212 | AGCATACGGCAGGAG[C/T]TCACAGTGATGTTCT | 58513 |
rs773086048 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425751 | TGGAGGCTGCAGTGA[A/G]CTGTGATCGCGCCAC | 58513 |
rs773089480 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413627 | TGAAAAAAAAAAAAA[A/C]AAAAACTTCATTCTG | 58513 |
rs773142702 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463471 | CACAGAGACTGTCTC[A/G]GAGCTAGAACCCAGC | 58513 |
rs773159492 | snp | C/T | 1.7187e-05 | 0.00293142 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361845 | AGAGGAGGGGACAAA[C/T]GGGTCTTTTCCACTA | 58513 |
rs773160556 | snp | A/T | 1.65337e-05 | 0.00287517 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442134 | CTGTGCTTTCAGCTC[A/T]GGCATGCTCTAGTTC | 58513 |
rs773186905 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16450569 | CACTGCAACCTCCGC[C/T]TCCCAGGTTCAAGTG | 58513 |
rs773189274 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421037 | CACAGCCAGCAAGAA[C/T]AGGGCCCAGCTGTGT | 58513 |
rs773194179 | snp | A/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472159 | GGCTGGGCCTGAGGC[A/T]TCTGCGTCTTCCGTG | 58513 |
rs773199928 | snp | A/T | 0.000236297 | 0.010867 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437066 | GGTGGGTGGGTTTGC[A/T]GAAAAGGATACACGT | 58513 |
rs773209404 | in-del | -/C | 1.64928e-05 | 0.00287161 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440833 | CTCTGCCCAGCCCCT[-/C]CATTTGCTCTGTGTA | 58513 |
rs773235368 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432054 | GTACATTTCGGTGTA[C/T]GATAGGGGCCCTGGA | 58513 |
rs773239462 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16390167 | ATCCAGGTAAGTTGA[A/G]AGTAAATGGTTGAAA | 58513 |
rs773281112 | snp | C/T | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436993 | TCAGAGGGCTGCTGG[C/T]GTCGTGCTGAGAAGA | 58513 |
rs773318474 | snp | C/T | 2.1482e-05 | 0.00327728 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428665 | GCACTGCACATTTCC[C/T]TCCTGGGCTGGGTGG | 58513 |
rs773327861 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429976 | GATGCCAGCAGCACT[C/T]GACCCAGGTGTGACA | 58513 |
rs773334710 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465031 | TTGCAGTGAGCCGAA[A/C]TTGCACCACTGCACT | 58513 |
rs773343045 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451496 | CTGTTAGAGGTGCAT[A/G]TTGAAATACAATTTC | 58513 |
rs773346711 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437372 | AAAACACGATGCTGA[C/G]AGAGAGGCCAGACAC | 58513 |
rs773433155 | snp | C/T | 6.66633e-05 | 0.00577297 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425155 | GACGCTGCCGTGGGA[C/T]GGCGTGGAGCGGAGG | 58513 |
rs773449632 | snp | A/C | 1.65784e-05 | 0.00287905 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413727 | AAGTTTTCCTGAACT[A/C]CATTTAGCACAAAGT | 58513 |
rs773465249 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361768 | GCCCGGAGGCGGAGG[A/G]CTCAACTTACAGAGG | 58513 |
rs773468992 | snp | A/G | 1.74178e-05 | 0.00295103 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421269 | ACAGTCTTCACCCAC[A/G]GGCCCCCTGGAGCCA | 58513 |
rs773488697 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16415201 | GTGAGGACACGGCAA[A/G]AAGGTGACTCTCCAG | 58513 |
rs773495990 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362827 | AAGTTCTTTTTTAGC[A/C]CCCACTTCTGTCCCT | 58513 |
rs773507409 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360874 | TGTTCAAAGAGCCAT[C/T]CCAGGAGTCGAAGCA | 58513 |
rs773531956 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414828 | AATCCTCCCACCTTA[A/G]CCTCCTGAGTAGCTA | 58513 |
rs773537971 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445593 | AACTGAAGACACATG[G/T]TGCTAATGACATAAA | 58513 |
rs773540636 | snp | C/T | 0.000192864 | 0.00981809 | missense, nc-transcript-variant, utr-variant-3-prime, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355710 | CGGCCCTCGCCTAGG[C/T]GGCAGGCATGTCAGC | 58513 |
rs773574575 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442095 | AAAGGACAAAAGGCC[A/G]CTCAGCCGGGCTTCT | 58513 |
rs773630964 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452447 | TGAAATTCCATCTCG[-/A]AAAAAAAAAAAAAAA | 58513 |
rs773676343 | snp | C/G | 0.000126231 | 0.00794352 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425266 | GAGGGACGGGGGCAG[C/G]GCGGAGGGCACGGGC | 58513 |
rs773705155 | snp | A/C/T | 3.29561e-05 | 0.00405921 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392333 | AAGGGTTTTTCGTGA[A/C/T]TGGATCCGAGGTAAA | 58513 |
rs773707084 | in-del | -/TAGG | 0.000119259 | 0.00772108 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437049 | CACAGAATTAAATCA[-/TAGG]TGGGTGGGTTTGCTG | 58513 |
rs773716687 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409866 | TCACTTGAACCTGGG[A/T]GGCGGAGGTTGCAGT | 58513 |
rs773750771 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379552 | CAGCAGACAGTCTTA[C/G]AGGTATGGCTGCCTC | 58513 |
rs773805733 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434241 | GAGCGCTGATGAAAG[C/T]CCCTGATGGCACAGG | 58513 |
rs773806626 | snp | C/T | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16395379 | TTAAATGGGTCAGAT[C/T]TGAAGGGGTCTTCTG | 58513 |
rs773808456 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444410 | GGTACAGGAAGGAGT[C/G]GCTATCACCCTTAGC | 58513 |
rs773834643 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464517 | AGACCTTCCTCCTCT[C/T]ATCCCTGAGCTGCCT | 58513 |
rs773839528 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421627 | AGGGCAGATGTGATC[C/T]TTGTTCTGTAACTGG | 58513 |
rs773839762 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413048 | GAAACAGACCCGCGC[C/T]GGCCAGTGCACCAGG | 58513 |
rs773852868 | snp | C/T | 1.69057e-05 | 0.00290733 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442028 | TTTCAGCAAATGCAG[C/T]AGCAGGTGAAGTGGC | 58513 |
rs773878060 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429933 | GCACTGCAGGGTGGT[A/G]AGCAGCATTCCTGGC | 58513 |
rs773882128 | snp | C/T | 1.67047e-05 | 0.00288999 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413851 | ATATTTCTCTCTGAA[C/T]GTTTAAAAATATTTC | 58513 |
rs773952196 | in-del | -/AAAAAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456686 | AAAACAAAACAAACA[-/AAAAAT]AGAGTCCTGGGCTTC | 58513 |
rs773968543 | snp | C/G | 5.27065e-05 | 0.00513327 | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361760 | GTGGGGTGGCCCGGA[C/G]GCGGAGGACTCAACT | 58513 |
rs773973167 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385671 | CCAAACACTGCTACC[C/T]GCCCCACGCAAGCTG | 58513 |
rs773986233 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465654 | ACCACTGTACTCCAG[C/T]GTAGGCAATAGAGCA | 58513 |
rs774036416 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442414 | TGCTTACCTGATTTA[C/G]AAAAAGTAAGCTTAA | 58513 |
rs774042883 | snp | A/G | 4.94792e-05 | 0.00497365 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417575 | CTGGGCAATCTCTTG[A/G]CTGATGTCATCAAGC | 58513 |
rs774076874 | in-del | -/T | 0.000345921 | 0.0131469 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394028 | GGAGAGAAATGCTTA[-/T]TTAGCTCTAGGGCAC | 58513 |
rs774122652 | snp | C/T | 1.658e-05 | 0.00287919 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418079 | CTTTGCTTAACTTCC[C/T]CGTTTGCCTCGTATC | 58513 |
rs774148892 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406059 | GAGGGGTGGGTTTGC[A/G]GGGAGCCATGGCTGG | 58513 |
rs774170697 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466548 | CCACTGCCCAGAAAG[C/T]GTCCAGCAAAAAGAA | 58513 |
rs774172948 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377176 | GAGGCAGAGCAGGAG[C/T]GTCCTGTTTACTTTT | 58513 |
rs774190555 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412967 | GCCCATCAAGGAATC[C/T]GAGATCATTGACTTT | 58513 |
rs774221727 | snp | C/T | 3.30704e-05 | 0.00406622 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441925 | CGAGAGGCCAGACTT[C/T]TTTAGAAAAAGCGCA | 58513 |
rs774234350 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470060 | CATTCAACAAATGTA[C/T]AGGGAAAGGAACAGG | 58513 |
rs774246358 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16396315 | TGTCCAGGTTGGAGT[G/T]CAGTTGCACACTCAT | 58513 |
rs774248284 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381246 | TGCCTTACACACAAG[A/G]AAACTGAGGCACACA | 58513 |
rs774296709 | snp | A/G | 0.000115501 | 0.0075985 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392270 | ACACAGAGCAGGCAC[A/G]CAGCTCTCCCGGGCA | 58513 |
rs774360940 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449932 | ATAATTCCATCACAT[A/T]ACATCATTAAAATGA | 58513 |
rs774361466 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372991 | GCCTAGCAGGGTTCT[A/G]GAAACCTCTGGGTGC | 58513 |
rs774361737 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409893 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 58513 |
rs774377706 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456979 | GGGGTGCCTGCAGGC[C/G]AGCAAGGTGGGCGCA | 58513 |
rs774420081 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366556 | GCTCTGTTGCCGAAA[-/C]CCGTTGTTATTTAGA | 58513 |
rs774427381 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401707 | AAAAATGTAAGGGGC[C/T]GACAGTCCCCTGCCC | 58513 |
rs774435194 | snp | C/T | 1.71784e-05 | 0.00293069 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434532 | AGTAGGAGAGCACAC[C/T]TGTGTGAATGTCCAG | 58513 |
rs774439435 | in-del | -/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361585 | TCCAAACTGCGGCTC[-/T]TTTTTTTTTTTATTG | 58513 |
rs774451723 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408262 | TAACCCCAACAGTCC[A/C]CGGAGTCCACACAAT | 58513 |
rs774485440 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448618 | GGAGGCCAAGGTAGG[A/C]GGATCACCTGGGGTC | 58513 |
rs774511750 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430286 | TCAGGGATGCTGTGG[C/G]GGTGTCTAATGGACA | 58513 |
rs774513433 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379366 | AGAAGAGAAAGATCA[C/G]AGTGGGGCAGAGGTG | 58513 |
rs774519603 | snp | A/C | 8.24681e-05 | 0.00642085 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440826 | CTGGGGGCTCTGCCC[A/C]GCCCCTCCATTTGCT | 58513 |
rs774530153 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408352 | TATGGGGCCAGGCAC[A/G]GTAGCTCACGCCTGT | 58513 |
rs774553353 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413044 | TGCAGAAACAGACCC[A/G]CGCCGGCCAGTGCAC | 58513 |
rs774569431 | snp | C/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16393981 | GCTGTTCTGCAAAGG[C/G]GTCATTCTGGAACGG | 58513 |
rs774571388 | snp | C/T | 1.72199e-05 | 0.00293422 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404798 | GGGAAAAATGAAGCA[C/T]GTCCAAGATAACGGG | 58513 |
rs774587859 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395330 | AATGAGAAAGTGGGT[A/G]GCAAGTGAGATACCT | 58513 |
rs774594188 | snp | C/T | 1.65072e-05 | 0.00287286 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436979 | GGGCGGTGTGACCAT[C/T]AGAGGGCTGCTGGTG | 58513 |
rs774595265 | in-del | -/GA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367972 | TAAACATGAGAGTGA[-/GA]GAGAGAGAGAGAGTG | 58513 |
rs774608733 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436644 | TGTGACCTAAAGATG[C/T]AAGATTTAAACTGCA | 58513 |
rs774665717 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385202 | AAGGGATCTAAGGTT[C/T]CAAAGGGATCTGCAA | 58513 |
rs774699164 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456065 | ATTAGCTAGGCATGG[C/T]GGCACAGGCCTGTAA | 58513 |
rs774724369 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365673 | CTCAGCCAGTCCCTC[A/G]AGCCCCTGCCTGCTT | 58513 |
rs774788689 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463278 | TCCTGGCTCCCTGAA[A/G]GTGGCCTCAACCTGA | 58513 |
rs774807678 | snp | C/T | 1.64936e-05 | 0.00287168 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440956 | ACTGCCGATCACTGT[C/T]CACGTGTTAACAAAA | 58513 |
rs774891076 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388450 | AAACTTCAAAAACTA[C/T]TGAAAACCAAAGATA | 58513 |
rs774908151 | in-del | -/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370564 | GCATTTGCACCCCAC[-/TG]AACACCAGATGATAA | 58513 |
rs774909400 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419661 | CCAAAAGAGAGCTGG[G/T]ACCGTTCTAACAGAC | 58513 |
rs774913181 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384446 | CTATTGTTGTTTTTT[G/T]ACTTGTCCATTCTGG | 58513 |
rs774926392 | in-del | -/AA | 1.6543e-05 | 0.00287597 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385085 | CATGACAAGAGGCAC[-/AA]AGACACTAGCAGAGG | 58513 |
rs774968955 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446300 | CTCTGATCCCCGCAC[A/G]TGGCCGAGGGCAGGA | 58513 |
rs775001998 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16444909 | TTTCTGTATTTTCAG[C/T]AGAAGCGAGGTTTCA | 58513 |
rs775028266 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391881 | GGTCCCCACCAGTGC[A/T]GTGTGTTACAAGGAC | 58513 |
rs775033962 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418218 | AAACAACGGCAGGGC[A/G]TGGTGGCAAGCCCCA | 58513 |
rs775039522 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432057 | CATTTCGGTGTATGA[C/T]AGGGGCCCTGGAACC | 58513 |
rs775049625 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404701 | CCTGTTTCTGAGCCT[C/T]GAGCTCCTGCAAACT | 58513 |
rs775091981 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467724 | GGGACAAGAGGACAA[A/G]TAAGTGTCCGAGCCA | 58513 |
rs775094909 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397912 | CTGTGATATTAAAAA[A/C]ACAGCACAACACCCT | 58513 |
rs775097500 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426660 | AGAACAACGACAACA[A/G]AAAAACAAAAAGTCC | 58513 |
rs775135664 | snp | A/T | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403837 | TTTCCTCCTGCTGCA[A/T]TCGGTTCAGCTCCGA | 58513 |
rs775139398 | snp | C/T | 1.80409e-05 | 0.00300336 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386180 | TCTCACCTGATCCTT[C/T]TGAGGAGACACTGGA | 58513 |
rs775157935 | snp | C/T | 2.2182e-05 | 0.00333025 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386278 | GCAGTTCGTTGGTTC[C/T]ATCACCCATTCATTC | 58513 |
rs775172507 | snp | A/G | 1.83239e-05 | 0.00302682 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425251 | CTTGGAGGGTGGGAT[A/G]AGGGACGGGGGCAGG | 58513 |
rs775179158 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409455 | GGTTCTCAGCTATGA[C/T]ACCAAAAGCAACAGC | 58513 |
rs775182629 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357440 | GTGGGCCCCAGGAAG[A/G]AGCTGGGATTTCCCC | 58513 |
rs775185162 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388193 | GATTACAAGTGTGCA[C/T]CACCACGCCTGGCTA | 58513 |
rs775186032 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363317 | AAAACCAGGAACTGC[C/G]TGTCCCTCCAGGGTT | 58513 |
rs775238079 | snp | A/G | 1.65075e-05 | 0.00287289 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16361998 | ACCTGGAAAGTTTAG[A/G]AGAAAAAAAAAAGGA | 58513 |
rs775295157 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378099 | TGTGGATTAATGGAC[A/G]AATGAATGGCGGGTG | 58513 |
rs775296576 | snp | C/G | 1.70699e-05 | 0.00292142 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434522 | AGCCCGAGTAAGTAG[C/G]AGAGCACACCTGTGT | 58513 |
rs775300319 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364620 | CCAGGCATGAGCCAA[C/T]GGTAAGCCAAGGCCT | 58513 |
rs775307748 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356888 | TCATCGGCCCCCTCA[A/G]GAAAGCTGCTGCTGC | 58513 |
rs775316951 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392013 | GTAGGAATGGGGATA[A/G]AGAAATAAGAACTAT | 58513 |
rs775324266 | snp | G/T | 1.70348e-05 | 0.00291841 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377099 | CGGTAGGCGGTGGCT[G/T]CGAGAGAAGAAAGCT | 58513 |
rs775324986 | snp | C/T | 3.2969e-05 | 0.00405998 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395306 | TCGACATAAAACACA[C/T]AGTCTTTCAATGAGA | 58513 |
rs775386517 | snp | C/T | 3.30153e-05 | 0.00406283 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417987 | AGGCGGGACCATGTC[C/T]GGCGAGAGGACTTGA | 58513 |
rs775386535 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16466186 | AGAGACAGGGTTTCA[-/G]CATGTTGGCCAGGCT | 58513 |
rs775386649 | snp | G/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16400813 | AATCTGTCTTTGGAG[G/T]TGGGGGAATCACTGG | 58513 |
rs775426750 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375661 | CCTGATGGTAAATGT[C/T]TTTGATGTGTGGCTT | 58513 |
rs775432430 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449085 | TCCAGACCAGCCTGG[-/G]CAACATAGTGAGACC | 58513 |
rs775437939 | snp | C/T | 4.94303e-05 | 0.00497119 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404673 | TCCATCTCGTCCAGG[C/T]GGTCTTGAGCATCCT | 58513 |
rs775439361 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460133 | TAAAAATCAGAAAAT[C/T]AGCTGGGCGTGGTGG | 58513 |
rs775440304 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404887 | TCAGGGCCAGCATTC[C/T]GTGCACACCCACGGC | 58513 |
rs775454143 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472353 | CGCCCACCCCGCGGA[A/G]GGTCGGGACCCTCAC | 58513 |
rs775486302 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16429332 | TCTCAAGCACCATCA[C/G]GCTGCCAGCTTCCTG | 58513 |
rs775489894 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371599 | TGACTGGCTGGTTAG[C/T]GGTAGAACTGCGCTG | 58513 |
rs775499311 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380920 | GAGATATGGCTGCCT[C/T]GGACCTTGTGTAGTC | 58513 |
rs775530047 | snp | A/C | 1.64727e-05 | 0.00286986 | splice-donor-variant | EPS15L1 | GRCh38.p7 | 19:16393950 | AAACACTGAATTTTA[A/C]CTGTTGAAGTTGTCT | 58513 |
rs775553308 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424029 | CTATAAACCCAACAC[A/G]GGGCAGCCTTGCCGT | 58513 |
rs775571644 | snp | A/C | 0.00016488 | 0.00907816 | utr-variant-5-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16471965 | CCGCGGACTCGGGCT[A/C]CGAGCGCCGGGGGAA | 58513 |
rs775610519 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16370142 | GGGAGCAAGTGAGGC[A/G]CAGAGCCCACCAGGA | 58513 |
rs775615743 | snp | A/T | 4.94703e-05 | 0.0049732 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434387 | AGGACATCAAGAGGC[A/T]GCTTTGAGTTCATGA | 58513 |
rs775620242 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403730 | CCCGACTCCGTGAAG[C/T]ACCTGGTTGATTTCG | 58513 |
rs775622183 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416260 | GTAAACAATCTCTTT[A/C]CCACAGAGGGCAAAG | 58513 |
rs775627701 | snp | C/T | 1.64844e-05 | 0.00287087 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404612 | CTCATCCTGGCACTT[C/T]TGCCGGACGTCGCTC | 58513 |
rs775647716 | snp | G/T | 1.70223e-05 | 0.00291734 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392486 | TTATACCAAGTGAAA[G/T]AACCCAGACATAAAA | 58513 |
rs775681886 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455771 | GGACTTGTCAATCAC[C/T]GGCTGTTGTGATTCC | 58513 |
rs775729464 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435753 | AACACTTGGCACTTC[A/G]GGCTTGTTCTTTCTG | 58513 |
rs775732220 | snp | C/T | 8.26754e-05 | 0.00642891 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385096 | GCACAAAGACACTAG[C/T]AGAGGCGCGGGGGCT | 58513 |
rs775748366 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470210 | AAAATGGTGAAACCC[C/T]GTCTCCACTAAAAAA | 58513 |
rs775750467 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431775 | TGGGATGATTACACA[C/T]TGTGTGCATGTATCA | 58513 |
rs775758427 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380247 | AGGCTCCAGTGTCTA[G/T]TTACAGCAATGCAGC | 58513 |
rs775764879 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16432628 | AATACAAAAATTAGC[C/T]GGCTGTTGTGGTGCA | 58513 |
rs775774997 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365961 | GGGCCCTTTGGAGCA[A/G]CACCCTGGGGAGCGA | 58513 |
rs775789187 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465426 | TGGTGGCTCACACCT[A/G]TAATCTCAGCGCTTT | 58513 |
rs775806376 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454997 | AGCCAGGTGTGGTGG[C/T]GCACACCTGTAATCC | 58513 |
rs775860556 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435293 | TGGTAAATAAATTAA[A/T]ACGTAAATAGGAATA | 58513 |
rs775939439 | snp | G/T | 1.65203e-05 | 0.002874 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437731 | CACACACACATCTGG[G/T]ATTAGAAGAATGTGA | 58513 |
rs775952546 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16418642 | CGGAACGTTTATGTC[C/T]CCCCAGATTCCTATG | 58513 |
rs775968763 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16405907 | CATTGTGACAAGCCT[-/C]CCTCCCTCCAGCTGC | 58513 |
rs775996027 | snp | A/T | 1.71687e-05 | 0.00292986 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402514 | ACATCATCAGCATTA[A/T]GCAGGGTCAGGAAAA | 58513 |
rs776019025 | snp | C/T | 4.96159e-05 | 0.00498051 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437845 | TGCACAGGCCACCAG[C/T]CTCAGTGCAACATAG | 58513 |
rs776025984 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385185 | TGAAGGACCCACTTC[C/T]GAAGGGATCTAAGGT | 58513 |
rs776036545 | snp | C/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401584 | AATGGGAAACTACAT[C/G]TCCCCAGGTTCGAGG | 58513 |
rs776053476 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387230 | AAAAACTTCATCACC[A/G]GGGTCAGTGGATCAC | 58513 |
rs776072303 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445253 | CCAACCTCTGCCCAT[C/T]CATGCTAAAGGCTCA | 58513 |
rs776082801 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397505 | CACTCAACAACAGCA[A/G]CACAGGCCTCATTTC | 58513 |
rs776144331 | snp | C/T | 3.2981e-05 | 0.00406071 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440836 | TGCCCAGCCCCTCCA[C/T]TTGCTCTGTGTACAT | 58513 |
rs776157231 | in-del | -/CT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359106 | GTGACCTGGGCCCCC[-/CT]CTGACTGCCAGCATG | 58513 |
rs776163044 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382132 | GGGCCAAGCCGGCTT[A/G]GCGCCTCCCATGTGT | 58513 |
rs776165793 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366583 | TAGAAATCATGACTA[C/T]GGTAATATGAAACCA | 58513 |
rs776172332 | in-del | -/AG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435698 | CGGACTTGCTGACTC[-/AG]AGTGCCTTCAGAAGC | 58513 |
rs776178566 | snp | C/T | 3.30098e-05 | 0.00406249 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440805 | GAGCCGTGGAGGTCA[C/T]CCAGCCTGGGGGCTC | 58513 |
rs776181828 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421407 | AGCCATCCAGGTCCA[A/G]GTCGGTCTTCAGGAA | 58513 |
rs776189471 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16356653 | ACAAAAGGTGTGGCA[C/T]TTACACTGCCATTTA | 58513 |
rs776263964 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407130 | AGTGCATGGTGTGCT[A/G]TTATGGCAAGCCAAA | 58513 |
rs776274888 | snp | C/T | 1.65471e-05 | 0.00287633 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417975 | GCCTCTCTCCGAAGG[C/T]GGGACCATGTCCGGC | 58513 |
rs776302300 | snp | C/T | 3.72745e-05 | 0.00431693 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386154 | AGTCAGGAAGAAAAA[C/T]AAGTCATGGGTCTCA | 58513 |
rs776308551 | snp | A/G | 4.94694e-05 | 0.00497316 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440932 | AACACAAAAATGCTC[A/G]TAAGCATGACTGCCG | 58513 |
rs776332861 | in-del | -/TTT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371391 | ACTTTTGTCTTCTTC[-/TTT]TGTTGAGAGAGCTGC | 58513 |
rs776339734 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454743 | ATTTAGACATGCAGC[-/A]AAAGCAGCAAGGTCA | 58513 |
rs776352956 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374666 | GGAGGCGGGGGTGGC[A/G]GTTTCCATGAAACAC | 58513 |
rs776408215 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16382991 | ACCTTCTTGCCACTT[C/T]CATTTCCCTTAGCAT | 58513 |
rs776426328 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393936 | AAGACCGGTCCGGGA[A/G]ACACTGAATTTTACC | 58513 |
rs776429665 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375516 | CTCCCATCTTTTAGG[C/T]AGAGTGAAGAGGCCC | 58513 |
rs776433047 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357365 | GTGAGGCTCAGTGCC[C/T]GACCTTGGGGTAGCC | 58513 |
rs776433713 | snp | C/T | 9.37251e-05 | 0.00684498 | utr-variant-5-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16471946 | GAGCGGCGCCGCCAT[C/T]TTCCCGCGGACTCGG | 58513 |
rs776435710 | snp | C/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403867 | ACTTGGCTCGGTTCA[C/G]ATCGTCTTCCTGGGA | 58513 |
rs776437086 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376256 | CGTCCCAGACCGGGG[C/T]ACAGATGGAACAGGC | 58513 |
rs776438870 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469721 | CCCTCCTCCCCTAGG[C/G]TAGCCCGCTGGGTTA | 58513 |
rs776445484 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378436 | GAACTCGGCCCACCT[C/G]GTCCACCAGGAACCC | 58513 |
rs776463184 | snp | C/T | 1.66813e-05 | 0.00288797 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361920 | GTCAGCCCCGAGTGG[C/T]TGGAATGGATCGGGG | 58513 |
rs776473591 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440365 | TTGATCCTGGGAGGT[A/G]GAGGTTGCAGTGAGC | 58513 |
rs776510427 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362314 | GCATGGCAACACATT[C/T]ATTAACATACTAATT | 58513 |
rs776570233 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16416161 | AGAATACTGCACCTG[G/T]TAATATGACCCCCGG | 58513 |
rs776601124 | snp | C/T | 1.66125e-05 | 0.00288201 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434351 | CAGAAGAACCAAGCC[C/T]GTGGCCCACTTACCC | 58513 |
rs776605898 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421810 | AAGCATGCCAGGAAA[C/G]ACCCTCCCGAGCACC | 58513 |
rs776623805 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16380188 | GTCACACAGACGTGG[C/T]CGTGTAAGGCTCCAG | 58513 |
rs776629926 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456619 | GCCAAGATGATGCCA[C/T]TGCACTCCAGCCTGG | 58513 |
rs776659855 | in-del | -/A | 0.000291492 | 0.012069 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442271 | CACAACCCCTTGGGG[-/A]AAAAAAGGGTTGCCC | 58513 |
rs776667224 | snp | A/G | 1.65209e-05 | 0.00287405 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404579 | GCCCCGGAGGTGGCC[A/G]GGACCCACCATCTGA | 58513 |
rs776680421 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16468018 | GGAAAGGAGGAAGGT[A/G]TAGCTCTTTGGGCCC | 58513 |
rs776694279 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414929 | CCAGGCTGGTCTGGA[C/T]CTCCTGGGCTCAACC | 58513 |
rs776694713 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426481 | TCTACTAAAAATTCA[A/G]AAAAAAAATTAGCTG | 58513 |
rs776715834 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454105 | AAGTGATGCAGGAGT[-/G]GGGGAAGGGTAAGAG | 58513 |
rs776743960 | snp | A/G | 1.65356e-05 | 0.00287533 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385089 | ACAAGAGGCACAAAG[A/G]CACTAGCAGAGGCGC | 58513 |
rs776776567 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403967 | TGTTAAAGAGATTCA[C/T]AGTGCAGGATGAAAT | 58513 |
rs776787898 | snp | A/C | 1.65425e-05 | 0.00287593 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442165 | CATCTGAAGAGACAT[A/C]AGCTAAACTTACCTG | 58513 |
rs776829866 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357329 | CTGACAGGGAGGATG[C/T]GTCCCTGCGAGGTTC | 58513 |
rs776837993 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437820 | TCAAGGTAACTTCAT[A/G]GCCACTCTGTGCACA | 58513 |
rs776870350 | snp | C/T | 1.78816e-05 | 0.00299006 | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16402270 | GGGATGTTCTGCTGT[C/T]ACACCAGGGGACCAG | 58513 |
rs776880434 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395943 | GAGTGAGTCTATCTC[-/A]AAAAAAAAAAAAAAA | 58513 |
rs776892940 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443457 | CTCACGCCTATAATC[A/C]CAGTACTTTGTGAGG | 58513 |
rs776896566 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472615 | TTGCAATCCAGCCTG[A/G]GCAACAGAAGCGAAA | 58513 |
rs776960200 | snp | A/G | 3.29679e-05 | 0.00405991 | synonymous-codon, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377225 | TCCTGCCCCTCCCAA[A/G]GAGGAGGTGAAAGGG | 58513 |
rs776974140 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16413821 | TTCCTTTTCTCGAAT[A/G]TCTTGTTCCAGTGAA | 58513 |
rs776975593 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433346 | CATGTTGGCCAGGCT[A/G]TTCTCGAACTCCTGA | 58513 |
rs777016752 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371481 | ACTGTGGGGAGGGGG[C/T]GAAAAGACATGCTCA | 58513 |
rs777091971 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358641 | GCCTCTTGGAAATCC[A/G]CAGTTTAGACAGCTC | 58513 |
rs777099670 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16401463 | GGAGGAGCCCTGGGA[A/G]AGAGGGTGGCAGCAC | 58513 |
rs777099894 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385770 | CGAGCGTGCATCTGC[A/G]AGTTCTACACTGTGA | 58513 |
rs777135640 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369989 | CCTACGGAGTGTGCC[A/G]ATGTCGCAGACGCCA | 58513 |
rs777141229 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442648 | AGGCCTGCAAGCTTT[C/T]GACCAGTTTCCCTGG | 58513 |
rs777149194 | snp | C/G/T | 9.9003e-05 | 0.00703516 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402369 | GACGCCTTCGCTCAG[C/G/T]TTGGCCAGGTCGGTC | 58513 |
rs777188059 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411224 | GGAACAGATGAAGGA[A/T]ATGTGCCCCATTGTG | 58513 |
rs777195021 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465354 | ATGGGCCAGGAGCAC[G/T]GATTACCACTCTGGC | 58513 |
rs777202746 | in-del | -/T | 1.68152e-05 | 0.00289954 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404775 | TTGCAGGGGTTTACG[-/T]TGAGGATGGGAAAAA | 58513 |
rs777213411 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16420032 | TACGGTGGCAGCCAT[C/T]GCAGGGAAAAAGCCT | 58513 |
rs777239943 | snp | C/T | 1.66743e-05 | 0.00288736 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404761 | ATTCCTAGGGAGGAG[C/T]TGCAGGGGTTTACGT | 58513 |
rs777240091 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361451 | GTTTGACATCTTGGC[C/T]TCCAAAAACCAGTGA | 58513 |
rs777241494 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422647 | TGCCACTCAAAGTCA[C/T]TCCTCTCAGTTATGA | 58513 |
rs777265869 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16454484 | CAGCATGAGCTGCTT[C/T]TGTAAATTAGACAGA | 58513 |
rs777271186 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399356 | CCAACTTGGGGGACA[C/T]GAGTACAGCAGACAA | 58513 |
rs777273556 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435531 | TCAACCACAATAAAA[A/T]TTTTTTAATTTTTAA | 58513 |
rs777312591 | snp | A/G | 9.88435e-05 | 0.00702937 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393932 | TCTAAAGACCGGTCC[A/G]GGAAACACTGAATTT | 58513 |
rs777318672 | snp | A/G | 2.27425e-05 | 0.00337205 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437099 | CAAAGTGCTTTCAAA[A/G]AAGGGAAGACTTCAC | 58513 |
rs777357907 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389530 | GTTCTTTAGGCTGAA[G/T]GAAAATGATAATGGA | 58513 |
rs777422666 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369216 | AGGCACCAGCCCCGC[A/G]CGCACTCTGCCTTAG | 58513 |
rs777452121 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453976 | AAGTGTGACAAATGA[A/G]GAGAGCTTGGTGACA | 58513 |
rs777466953 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431496 | TTTAGTAGAGATGGG[C/G]CTTCACCATGTTGGC | 58513 |
rs777483235 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16360490 | ACATGGGCCAGTCAC[A/G]TGTAACCCCAGTACT | 58513 |
rs777489902 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427992 | GTGGATCACTAGGCA[A/G]GAGATCGAGACCATC | 58513 |
rs777489974 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388096 | CACCCAGGCTGGAGC[A/G]CAGTGGTGCAATCTC | 58513 |
rs777520917 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16436944 | TCACTTACCCTCACA[A/G]CCCAGTGGGCCTCTG | 58513 |
rs777525428 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386555 | CAGGAGGTTGAGTTT[C/T]CATTCCGCCAGCTAC | 58513 |
rs777532391 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445112 | AGAGTTTCAGTCTTT[A/G]AGGCATGCAGGGTTA | 58513 |
rs777537464 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16357281 | TAGACTTTTTCCCCC[C/G]CAGGCCTGTGGGGAG | 58513 |
rs777537664 | snp | C/T | 6.60338e-05 | 0.00574566 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421351 | GTTCTGGGTGAGGCC[C/T]GAGTGCATGAAGATC | 58513 |
rs777578057 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424464 | GGCCCCACTAGCTTC[A/G]TTGCCAGTAAAGTAC | 58513 |
rs777605350 | snp | A/C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409217 | GCCTCGGCAACAGAG[A/C/T]GAGACTGTCTCTAAA | 58513 |
rs777615550 | snp | C/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16384265 | CACACCTCATCTGCT[C/T]TCCTTCATTCCTGCC | 58513 |
rs777653937 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16408151 | ACCTGGACCTCATTC[C/T]GTAATGGAGAAGGAG | 58513 |
rs777671794 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452943 | CTAGGACTACAGGTG[C/T]CCACCACCATGCCCA | 58513 |
rs777681365 | snp | C/T | 1.6766e-05 | 0.00289529 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417519 | AGTTCGTGTAACATC[C/T]GGATGTGGAGGGAAG | 58513 |
rs777700234 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16452921 | CCTGCCTCAGCCTCC[C/T]GAATAGCTAGGACTA | 58513 |
rs777739634 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16439735 | TGCAGACATGCACCA[C/T]GAACCTCAAAGAAGG | 58513 |
rs777780328 | snp | C/T | 1.6516e-05 | 0.00287362 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385240 | CAACAAAGTCAGAGT[C/T]ACAGGTCTTTAAGAG | 58513 |
rs777786847 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404488 | ATTGACCCAGTAGGA[A/T]GTCTAAGTGTTGTGT | 58513 |
rs777828925 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16463988 | CCAGGGGGCCACAGA[A/G]CAGAGGGAATGAGGA | 58513 |
rs777853048 | in-del | -/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16382951 | AAAAGTTGATGATGG[-/T]TTTTTTTTTGTTTTT | 58513 |
rs777864892 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459632 | GAGAATAGACAGCAC[A/C]TGGCCTGAGGATGCT | 58513 |
rs777875657 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384337 | CACAAGGAAGCACAA[C/T]GGTGCCGCAGCCCTG | 58513 |
rs777877020 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458657 | CATCTCCTACCTTGC[C/T]GGGCTGATTTCACTC | 58513 |
rs777900950 | snp | C/T | 0.00113058 | 0.023749 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16471893 | CCCCGGCGCCGCCCC[C/T]AGGCCCGCCCGGCCC | 58513 |
rs777914313 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472652 | CTCAAAAATAAATAA[A/G]TAAATAAGACAAGAA | 58513 |
rs777916550 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16459045 | GCGTGGCCCGGTACA[A/G]AAAACTGCAGGCAAC | 58513 |
rs777944374 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447490 | CAGGGCCAGGCACTC[C/T]GGCTCACACCTGTAA | 58513 |
rs777946511 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384883 | CTGAGACCTGATGGT[C/T]GTCAGACACCAGTGG | 58513 |
rs777966812 | snp | A/G | 1.6617e-05 | 0.00288239 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417632 | GCCGAGAGAGCCTGA[A/G]CTGTCCTAGAATTGA | 58513 |
rs777984888 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362934 | CCCGGTCCCAGCAAG[C/G]TATATCTTGACAGGG | 58513 |
rs778036780 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375374 | AGCATACACGTGTAC[A/G]TGCACATACATGCAT | 58513 |
rs778071843 | snp | A/G | 3.30775e-05 | 0.00406665 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385080 | CACACCATGACAAGA[A/G]GCACAAAGACACTAG | 58513 |
rs778080074 | in-del | -/AGC | 1.65213e-05 | 0.00287409 | cds-indel, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377147 | TTTAGGCCGTGGAGG[-/AGC]AGGTTTCTTCGGAGG | 58513 |
rs778100840 | snp | C/T | 1.66424e-05 | 0.0028846 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441903 | ATACCTTCCCAAGGA[C/T]AATGTCCGAGAGGCC | 58513 |
rs778108075 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437786 | AATTTAGGCGGTGGC[A/G]TGCTCAAATTCAGAT | 58513 |
rs778115246 | snp | C/T | 1.65556e-05 | 0.00287707 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16441973 | CCTCCCTGTGTATGC[C/T]GGATCGACCTGAAAT | 58513 |
rs778137057 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427359 | GACCACAGGGTTTCA[A/G]TTCTGGAGTTTTCTG | 58513 |
rs778161324 | snp | A/G | 4.94923e-05 | 0.0049743 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385150 | CATCTGGCTGAAGTC[A/G]GCAAAGCCTTCAGCA | 58513 |
rs778164294 | in-del | -/GGG | 1.67156e-05 | 0.00289093 | cds-indel, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425183 | AGGCTGTCTTTTGGT[-/GGG]GGGCTGGCAGGCAGG | 58513 |
rs778168530 | snp | A/T | 1.68644e-05 | 0.00290378 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361872 | ACTAAACGGGTCCCC[A/T]AACCCCTTTTTACTT | 58513 |
rs778171155 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465872 | ACTTTCCAAGACAAG[A/T]AACTATGGTGCAATG | 58513 |
rs778195485 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448278 | GTTCATGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 58513 |
rs778201995 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436579 | TTGCAAGCTCTCACC[A/G]TTTCCTCTTCTATTC | 58513 |
rs778222025 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386929 | GACTACAGTCTCTAC[A/C]CAGAACGCTCACCAT | 58513 |
rs778233348 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411175 | TATTCACAACAGCCA[A/G]AAAGTGGGAAAACCC | 58513 |
rs778233865 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391702 | AATATGCAAAATACC[C/T]GGTGTCTGCCACGCC | 58513 |
rs778237484 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467102 | ATCTAAGGACCTAAA[C/T]ATTGAAAAGCAGGCA | 58513 |
rs778253640 | snp | A/G | 4.95348e-05 | 0.00497644 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403887 | TCTTCCTGGGACTTT[A/G]AGTCAGATTCCTGAG | 58513 |
rs778290188 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453888 | AAAAGAATTCCTATA[-/A]AAAAAAAAAAAAGGC | 58513 |
rs778332267 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372530 | CTCCCTGCACGCTTT[G/T]TTTAACGGAAAAGAT | 58513 |
rs778360158 | snp | C/T | 4.94743e-05 | 0.0049734 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421452 | GCATCTTGTCTGCCA[C/T]GGGCACCACCCAGTT | 58513 |
rs778361030 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393926 | ACACAGTCTAAAGAC[C/T]GGTCCGGGAAACACT | 58513 |
rs778365121 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456447 | GGATCACATGAGGTC[A/G]GGAGTTCGAGACCAG | 58513 |
rs778419714 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445010 | AGGCATGAGCCACCA[C/T]GCCCAGCCCCAGGCG | 58513 |
rs778422348 | in-del | -/GGCCA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419975 | GGTGGCTCAGTCAGC[-/GGCCA]GGCCATCCGGCTCTG | 58513 |
rs778541349 | snp | G/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392412 | ACGGAATGGGTCACT[G/T]TCTTTGAAAGGGTCC | 58513 |
rs778593048 | snp | A/C/T | 6.89505e-05 | 0.00587122 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442265 | AGTGAACACAACCCC[A/C/T]TGGGGAAAAAAAGGG | 58513 |
rs778639035 | snp | C/T | 1.65463e-05 | 0.00287626 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377294 | GGCAAAAATAGTTGT[C/T]AAAACAAAGGTGACG | 58513 |
rs778656704 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361630 | TTACAGAAGTGGCAG[C/T]GTAGAATAAATAACG | 58513 |
rs778662657 | snp | G/T | 1.75591e-05 | 0.00296298 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437058 | AAATCATAGGTGGGT[G/T]GGTTTGCTGAAAAGG | 58513 |
rs778667162 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366937 | TTAATCGTTTTTTCC[A/G]ATTTTGTGAGGTATA | 58513 |
rs778681075 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16437779 | ACTCACAAATTTAGG[C/T]GGTGGCATGCTCAAA | 58513 |
rs778693052 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419840 | GGCCCCAGCCTGCTC[A/G]TGGGCTGCAGCTGCC | 58513 |
rs778723804 | snp | C/T | | | | | GRCh38.p7 | 19:16405361 | CTGCGCTGGGCTCTG[C/T]GGTGGGGAGCCCGGT | 58513 |
rs778723988 | snp | C/T | | | | | GRCh38.p7 | 19:16378271 | ATGCAGGGACTTCAT[C/T]GCTGCCCCAGCTGCC | 58513 |
rs778727961 | snp | A/G | 1.68153e-05 | 0.00289955 | | | GRCh38.p7 | 19:16361961 | AGTCTGCGGAACCAA[A/G]CTGGCTTACAGGTGT | 58513 |
rs778744739 | snp | C/T | | | | | GRCh38.p7 | 19:16359350 | GCTGATCGGCTGAGC[C/T]CCCGAATGCCGTGAA | 58513 |
rs778769265 | snp | C/T | 3.31741e-05 | 0.00407259 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421330 | TTACCATATGTGTGC[C/T]AGAAGGTTCTGGGTG | 58513 |
rs778816861 | in-del | -/AA | 1.66128e-05 | 0.00288204 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421494 | GAAACAGTTTTTGGC[-/AA]AACAGTTAATCTGGA | 58513 |
rs778869054 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451231 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 58513 |
rs778869065 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16431020 | AAGGCAGGCGGATCA[C/T]CTGAGGCCAGGAGTT | 58513 |
rs778896430 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16435037 | CAACTTCCGACTCCC[A/G]GGTTCAAGCAATTCT | 58513 |
rs778901189 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419240 | GAGGCGGGCAGATCA[C/T]CTGAGGTCAGGAGTT | 58513 |
rs778901902 | in-del | -/AAAT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393692 | ATAAATAAATAAATA[-/AAAT]AAATAAATAAATTAG | 58513 |
rs778917094 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387508 | GCTACTTGGGAGGCC[A/G]AGGCAGAAGAATCAC | 58513 |
rs778935849 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16387823 | AACCAAGAATAAAAG[A/C]AAGAGTAAGTGAAGT | 58513 |
rs778997163 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374428 | ATTGTGCAACAGCTC[C/T]CTAAAAAGCCTGAAC | 58513 |
rs779002070 | snp | A/G | 3.85134e-05 | 0.00438808 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | EPS15L1 | GRCh38.p7 | 19:16361792 | ACAGAGGTGAAGTCT[A/G]CAAAGCCCGAGGCAG | 58513 |
rs779002480 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16425374 | GGCCGGGACCATCAG[C/G]AGAAGGCAGAGGGCA | 58513 |
rs779052286 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426324 | ACTCCATAACTGCTG[A/G]CCTGTGCTCTTCAAA | 58513 |
rs779057844 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438338 | AGGCTGGGCAAAAAG[A/G]GCAAAACTCCGTCTC | 58513 |
rs779066558 | snp | A/C | 3.09076e-05 | 0.00393101 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425297 | TCCTTCTCCAGGGCT[A/C]GGTACACCAAGTGCA | 58513 |
rs779081553 | snp | G/T | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383983 | ACCTTCAGGCTGACA[G/T]CAGCGCTCACAGGGA | 58513 |
rs779110548 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368271 | ACACACACACAAGCA[A/T]CACTGATCCTACACA | 58513 |
rs779111985 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372536 | GCACGCTTTTTTTAA[C/T]GGAAAAGATTTCCAC | 58513 |
rs779198024 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398410 | CAGTGCTGAGTGGAC[A/G]TCAGGTGCTGACGAC | 58513 |
rs779202495 | in-del | -/AAG | 6.04638e-05 | 0.00549802 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362009 | TTAGGAGAAAAAAAA[-/AAG]GAGAAAGAAAGAAAT | 58513 |
rs779220008 | snp | C/T | 3.29919e-05 | 0.00406138 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403878 | TTCAGATCGTCTTCC[C/T]GGGACTTTAAGTCAG | 58513 |
rs779234650 | snp | A/C | 1.81691e-05 | 0.003014 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413891 | AGAGTGAATAATAAG[A/C]CTCCACCCCTTCCCA | 58513 |
rs779236467 | snp | G/T | 1.65091e-05 | 0.00287303 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395490 | TTTGTGAAGAAACAG[G/T]ACAGGGATTTTATTA | 58513 |
rs779242871 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389653 | AATACCCACAATGGA[-/T]TAATACAAAAATTGT | 58513 |
rs779252891 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397106 | TTCTTTTTTTTTTTC[C/T]GAGACAGAGTTTCAC | 58513 |
rs779272123 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391477 | GTGAGCGAGGTGGGC[A/G]CCAGGGTAGCAGGAG | 58513 |
rs779279263 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447149 | GGGTGAGATAACCTG[A/G]CTCAGTCATGTGGCA | 58513 |
rs779302560 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16418033 | TTACTGACCTTCTGC[C/T]GAATGAAATACATAG | 58513 |
rs779321753 | snp | A/G | 9.80498e-05 | 0.00700109 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386249 | AAATGAAAGGAGAGA[A/G]GAAAGAGTAAAAAGC | 58513 |
rs779322118 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375197 | GTGTGTGCCTGCATA[A/T]GCGTACATGCAGGCA | 58513 |
rs779329410 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363766 | GCCAGTGAGAACCTG[A/G]CCCGTAGCCCCCCCT | 58513 |
rs779361771 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448205 | TCACAAAAGGAAAGA[C/T]TGGCAGACAAACTTT | 58513 |
rs779362128 | in-del | -/GG/GGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448547 | CGTATTAAAAAAAAA[-/GG/GGG]GGGGGGGGGAGAAAG | 58513 |
rs779362147 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440921 | ATATCTGCGGAAACA[C/T]AAAAATGCTCATAAG | 58513 |
rs779362243 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403407 | ACTTTGTCCCTCTTG[C/T]TTGTGTGAGGACCAG | 58513 |
rs779375505 | snp | C/G | 1.67511e-05 | 0.00289401 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421521 | CTGGAAGCTTTTTAT[C/G]ACCCCCAGACACATG | 58513 |
rs779388450 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403787 | GATGGTTTCCAGCTG[A/G]ACTCGCCCAGCCTGA | 58513 |
rs779395660 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449687 | TCATGTTCATACCAC[A/C]TCCTGTATGCAGTGT | 58513 |
rs779411366 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16392290 | TCTCCCGGGCAACGT[C/T]CCACCCCACTCACCT | 58513 |
rs779429694 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433948 | AGCCTAGGCAACAGA[A/G]CAAGACTCCATCTCA | 58513 |
rs779441288 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411084 | CTGACAGGAAATGTC[C/T]GGAACTCCAGGTACC | 58513 |
rs779451138 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442121 | CTTCTATTCTGTACT[C/G]TGCTTTCAGCTCAGG | 58513 |
rs779467040 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451529 | TTATTTATTTATTTT[-/A]TTTTTTTTATTTTTT | 58513 |
rs779504709 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16465817 | AAACAAATGAGGTTA[A/G]GAGATGTCATAAACT | 58513 |
rs779558153 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16455410 | GGATTACAGGCATGA[A/G]CACCAAACTCAGCAT | 58513 |
rs779575612 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411891 | TTTTGTAGAAACAGG[C/G]TCCCACTGTGTTGCC | 58513 |
rs779610987 | snp | A/C | 1.66471e-05 | 0.00288501 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441995 | ACCTGAAATGGGAGA[A/C]CAAGAGGCAAAATAA | 58513 |
rs779664073 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16447469 | TCACTAGTAATTTAA[G/T]TATTACAGGGCCAGG | 58513 |
rs779664674 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16407902 | CCTGGGCCAGAAGGG[A/G]TGGCTGCTGATGGGA | 58513 |
rs779676665 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419201 | GCAATGGCTCATGCC[C/T]GTGTTCTCAACACTT | 58513 |
rs779690003 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16382405 | GGGCTCTCTGGGCTC[A/G]GCAAGAGTGAAGTGT | 58513 |
rs779702042 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371026 | TGTACCCACCGGATT[A/C]TCTCTCTGAGATCAT | 58513 |
rs779730034 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16430898 | CAGATGAATGGATCA[C/T]AGGGATGCGGAGGGA | 58513 |
rs779744165 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460673 | GACCCACAGAGAAAG[C/T]TTCCAAAGCCAGCAC | 58513 |
rs779753877 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469585 | ATTTACGTTGATATT[C/T]AGGGTCAGAAAAGAG | 58513 |
rs779755372 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369520 | TGCCATTAAAAGAAG[A/T]AAGTGGGGAAAAGGT | 58513 |
rs779760130 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409245 | AAAAACAAATTTTTT[A/T]AAGTAAAATAATAAA | 58513 |
rs779767076 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377536 | CACCAAGGGCATCCC[C/T]AGTCACACGAGGCAC | 58513 |
rs779780264 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379986 | TGAGGCTCTAGCTTC[C/G]AGTCACACCAATGCA | 58513 |
rs779816749 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392328 | TAAGGAAGGGTTTTT[C/T]GTGAATGGATCCGAG | 58513 |
rs779816913 | snp | C/T | 1.65701e-05 | 0.00287833 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404563 | CTGTGCATAGGGCGC[C/T]GCCCCGGAGGTGGCC | 58513 |
rs779900053 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377159 | AGGAGCAGGTTTCTT[C/T]GGAGGCAGAGCAGGA | 58513 |
rs779944941 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385502 | TGGGTCCCACTGGGT[A/C]TCAATGGGTCAGGAG | 58513 |
rs779955387 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16458528 | GCCCTGCCTTCACCC[A/G]CTTCCCCACTGCACC | 58513 |
rs779966074 | snp | C/T | 1.64871e-05 | 0.00287111 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16413769 | AAACGAACGAGACCC[C/T]TACCTGCACCTCGCT | 58513 |
rs779976858 | snp | A/G | 3.40304e-05 | 0.00412481 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402322 | TATTCAACCTTTACC[A/G]TGGCTCCAAAACTGC | 58513 |
rs780004137 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16443234 | GCAGGGAAAAGAGGA[C/G]TATCTTGGGGGCAGG | 58513 |
rs780062357 | snp | A/G | 3.30551e-05 | 0.00406528 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377277 | AGAGGACATGAAAGA[A/G]AGGCAAAAATAGTTG | 58513 |
rs780064994 | snp | A/G | 0.000194875 | 0.00986911 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355670 | CCCTCTCTGGAACCC[A/G]CCCGTGCCCTGTCCC | 58513 |
rs780074418 | snp | C/T | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473968 | CCGTCTCAAAATAAA[C/T]AAATAAATAAAGCAC | 58513 |
rs780083359 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403754 | GATTTCGTCTTGCGT[C/T]GACTTCAGGGACTTG | 58513 |
rs780087442 | snp | A/C | 1.91918e-05 | 0.00309767 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16386129 | GGAGCTCTGCTACTG[A/C]CCAAGGAATAGTCAG | 58513 |
rs780087900 | snp | G/T | 5.15796e-05 | 0.00507811 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16437052 | AGAATTAAATCATAG[G/T]TGGGTGGGTTTGCTG | 58513 |
rs780092253 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456720 | TCAGGAAGGGCAGGC[-/G]GGACAAAGTCAGCCC | 58513 |
rs780114345 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16438038 | CACCTTGGGGACATC[A/G]CTTAAATGAATACAC | 58513 |
rs780116455 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16381828 | CTGGGCCTAGGGCCC[A/G]TGCGAGTCCCCCGCG | 58513 |
rs780144432 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16359423 | ATGGATGATTTTAGA[A/C]AATGATACGACCCAA | 58513 |
rs780153554 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467493 | AGGTGGAGGGGTCTT[G/T]CCCAGGGAGAATCTA | 58513 |
rs780173380 | snp | A/G | 3.71519e-05 | 0.00430982 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16386229 | GGATTCAAAGGGGTC[A/G]AGCTAAATGAAAGGA | 58513 |
rs780179829 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355867 | CTGCAAAGGAAAAAC[A/G]GAGAGTGGGTGATGT | 58513 |
rs780184218 | snp | A/G | 1.73378e-05 | 0.00294425 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16441865 | AGGGCAGCCACAGAA[A/G]AGAAATCACTATTCA | 58513 |
rs780215283 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16397011 | GCTGGGTTCCACAAC[A/G]ATGTGAATATACCTA | 58513 |
rs780231425 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366862 | TTATTTTTAGCGGCT[A/G]TATTTTTCAAACCTT | 58513 |
rs780243842 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436884 | CTAGAACAACTGCTG[A/G]AACAATTCTATCTGA | 58513 |
rs780264859 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16440903 | CTGGATCGGCCAAGT[C/T]CCATATCTGCGGAAA | 58513 |
rs780278041 | snp | C/G | 3.37798e-05 | 0.00410959 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16404784 | GTTTACGTGAGGATG[C/G]GAAAAATGAAGCATG | 58513 |
rs780279773 | snp | C/T | 1.74525e-05 | 0.00295397 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417681 | TAATTAGCAACCTGA[C/T]ATCACCTGACAGGAG | 58513 |
rs780289075 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16378074 | AGTTGGATGAATGGA[C/T]AGACATATATGTGGA | 58513 |
rs780315085 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451152 | GACCGGGTCTCACCA[C/T]GTTGGCCAGGCTGGT | 58513 |
rs780324585 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16374225 | ATGGGCATGGCCTGG[A/C]CTGTCTCCCTCACGG | 58513 |
rs780326031 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440022 | GCAGTGAGCCAAGAT[C/G]ATGTCACTGCACTCC | 58513 |
rs780342906 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16402596 | ACCCAGACTGGAATG[C/T]AGTGGAGTGATCATA | 58513 |
rs780386817 | snp | C/T | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16361555 | CTGGAAGAAAACGTG[C/T]CCTTATGATAGAGCA | 58513 |
rs780402002 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406575 | TAACGCTGGCAGCAA[C/T]TCCCTGGTGTCCTGG | 58513 |
rs780433515 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369290 | TGAGGTCCCTGCGAT[C/T]GCAGCGTTGAGATTT | 58513 |
rs780453755 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375071 | CAGTATGTGAGTGCA[C/T]GCTGCTCATCTCTAT | 58513 |
rs780458175 | snp | C/T | 1.67027e-05 | 0.00288982 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16434487 | ATTTGGCCTTTTCTT[C/T]CACCTAGTTGGAAAG | 58513 |
rs780466506 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16423749 | ATGGGCTTGCTGCCT[C/T]TTAAGTCACGGAGCT | 58513 |
rs780469035 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462154 | TTTACCTCTCTCCCT[C/T]TCAGTTTCCTCATCT | 58513 |
rs780480174 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16469086 | TGGGCAAGTAGGAAG[C/T]AGAATGGCCCAGACC | 58513 |
rs780484491 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16393872 | CCCGGTGTATGTGGA[C/T]ACAAGTCCCACCACA | 58513 |
rs780484516 | snp | C/G/T | 5.00507e-05 | 0.00500233 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16417957 | ACTCACCGGGCCGGG[C/G/T]GTGCCTCTCTCCGAA | 58513 |
rs780501401 | snp | A/C | 0.000280878 | 0.0118474 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403716 | GCATGTGGCAGGGAC[A/C]CGACTCCGTGAAGTA | 58513 |
rs780509749 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16426222 | GCCCATGTGGGGCGG[A/G]TGTGACCTCCGTGGG | 58513 |
rs780551594 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368746 | ACACAACAGGTGATC[C/T]CACAAAACCATCATT | 58513 |
rs780552603 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422028 | CACACACGTCACTGA[A/C]AGGTAACAAATGAGA | 58513 |
rs780557760 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358540 | TGGAACCGAGACACC[A/G]TAGGGGCATGACACC | 58513 |
rs780582035 | snp | A/G | | | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16421352 | TTCTGGGTGAGGCCC[A/G]AGTGCATGAAGATCT | 58513 |
rs780587727 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16446171 | TTCACACAAGCGCCT[G/T]TAACTGTAACCCAGG | 58513 |
rs780633474 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391301 | GCTGGTTATGGGAAA[A/G]GTCAATGAAATTGGT | 58513 |
rs780635755 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16372922 | GAGGACAGAAGGAAG[C/T]GGCCTCAGTTCTCCT | 58513 |
rs780644591 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409285 | GCCATGACAACTAGA[C/T]GTCCACATGCAAAAC | 58513 |
rs780662847 | snp | C/T | 5.19476e-05 | 0.00509619 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16377091 | TCCGGCACCGGTAGG[C/T]GGTGGCTGCGAGAGA | 58513 |
rs780704977 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16433654 | CACAGTGAGACCCCA[A/T]CTCTAAAAACTCAAA | 58513 |
rs780737254 | snp | A/G | | | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16356074 | GATGCATGTGATTGA[A/G]TGTGACCTTAACCAT | 58513 |
rs780750731 | snp | C/G | 1.65162e-05 | 0.00287365 | missense, intron-variant, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16377149 | TAGGCCGTGGAGGAG[C/G]AGGTTTCTTCGGAGG | 58513 |
rs780763471 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456763 | CAGGGGACCGCATGA[C/T]ATGACTGCAGCAGTA | 58513 |
rs780792338 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16379933 | CACAGACACGGCCAT[A/C]TAAGACTCCAGTGTC | 58513 |
rs780830578 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362851 | TGTCCCTCTGGTGTT[C/G]GTGGCTCCAAGGGGC | 58513 |
rs780845793 | snp | A/G | 9.95586e-05 | 0.00705474 | synonymous-codon, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16425107 | CTTGAGGCTGTGCTT[A/G]GGGGACAGGCTCCCT | 58513 |
rs780926120 | snp | A/G | | | intron-variant, utr-variant-3-prime | EPS15L1 | GRCh38.p7 | 19:16383696 | TGCTGCGCCGCCAGG[A/G]CACGCACACACGCGT | 58513 |
rs780938965 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411199 | AAAACCCAAATATTC[C/T]CCGATGGGAGGAACA | 58513 |
rs780951447 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16403807 | GCCCAGCCTGAATGC[C/T]CTGCTCCAGCTGGGT | 58513 |
rs781007939 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16404665 | TCTGCTGGTCCATCT[C/T]GTCCAGGCGGTCTTG | 58513 |
rs781013023 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16389755 | TGGCTGCAAGGGTGG[A/G]TGGACAAATGGACCT | 58513 |
rs781030771 | in-del | -/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16409511 | CACCAACATTAACAA[-/C]TTGTGCTTCAAAAGA | 58513 |
rs781034712 | snp | A/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16399793 | TCCCAAAGGACTGGG[A/T]TTACAGGTGTGAGCC | 58513 |
rs781066726 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16406542 | CCTCCTAAGTCTAAC[C/G]CTGGCCCCATCACCG | 58513 |
rs781071553 | snp | A/T | 1.6477e-05 | 0.00287024 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16394048 | CTCTAGGGCACAGGA[A/T]GCGGGCCGGGCCCTT | 58513 |
rs781086056 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16410479 | ACAGTTACCATGTGG[A/C]CCAGCAAATTCACTC | 58513 |
rs781086633 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16417061 | CAAGGATAACAAGGC[C/G]TTCCTAGCACTGGGG | 58513 |
rs781093747 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358181 | GCGCCTTCCCTTGAC[A/G]GGTCTGTGTTTCCAA | 58513 |
rs781101518 | snp | C/T | 1.67139e-05 | 0.00289079 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16402460 | TCCTGGCGGCTTTCA[C/T]GCAGCTGGGAAAGTT | 58513 |
rs781106187 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16384372 | TCCCACTCACCACAG[A/C]CCCCATTTCCAACTT | 58513 |
rs781120668 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16434244 | GCTGATGAAAGCCCC[-/T]TGATGGCACAGGGAG | 58513 |
rs781138759 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16470758 | ACTCTCTTTGGGTTT[A/G]GAATTCTTAATTGCT | 58513 |
rs781139665 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16427584 | GAACTATGTCAAGAC[A/G]AACACTTAAAAAATG | 58513 |
rs781145216 | in-del | -/AAAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16388830 | AACTCTGTCTCAAAA[-/AAAC]AAACAAACAAACAAA | 58513 |
rs781173129 | snp | A/C | 0.000183773 | 0.00958398 | intron-variant, downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355900 | CCCTGGGGCTGGGAC[A/C]TGCAAGCTGGAGGGA | 58513 |
rs781184423 | in-del | -/GACA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364331 | AGCCCACGCGGGCAG[-/GACA]GACAGGAATGTGGCC | 58513 |
rs781191687 | snp | A/T | 3.2981e-05 | 0.00406071 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16385168 | AAAGCCTTCAGCACT[A/T]TTGAAGGACCCACTT | 58513 |
rs781272643 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16449468 | GGCTAAAATAACAAA[C/T]AGTGACAACATCAAA | 58513 |
rs781313484 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16368163 | CACCTTCGCTATTAT[C/G]CTATACAACACAGAA | 58513 |
rs781324881 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16448398 | AGCCAGGCATGGTGG[C/T]GCATGCCTGTAATCC | 58513 |
rs781395589 | snp | A/G | 1.65562e-05 | 0.00287712 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16403711 | CCCTGGCATGTGGCA[A/G]GGACCCGACTCCGTG | 58513 |
rs781409993 | snp | C/T | 1.65477e-05 | 0.00287638 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16385260 | GTCTTTAAGAGAACA[C/T]GCCTTCTGGGGTGGA | 58513 |
rs781410160 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460501 | TAAAGTCAACTGACT[A/G]TAAATGCCAACTCAG | 58513 |
rs781413799 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365301 | TAACCCCTGTGCCTT[A/G]GAATATAACCATACT | 58513 |
rs781426372 | snp | A/G | 1.66707e-05 | 0.00288705 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16421509 | AAAACAGTTAATCTG[A/G]AAGCTTTTTATGACC | 58513 |
rs781427138 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412432 | TTGAACCCAGGAGGC[A/G]GAAATTGCAGTGAGC | 58513 |
rs781463314 | in-del | -/AACACA/AACACTAACACA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464746 | ACTAACACTAACACT[-/AACACA/AACACTAACACA]AACACTAACACTAAC | 58513 |
rs781468665 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364400 | CCCACACCCGAGCTT[C/T]CTAGGTGTCTCCCTT | 58513 |
rs781538583 | snp | A/G | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16473891 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 58513 |
rs781541123 | snp | C/T | 2.07213e-05 | 0.00321873 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16428734 | GATCCAAGTGCCCAT[C/T]CTTGTCAATGTCACT | 58513 |
rs781574426 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16395083 | AAATTAGCCGGGTGC[A/G]GTGATGGGCGCTGAG | 58513 |
rs781583705 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414089 | CGCGCTTTCTCCACC[C/T]GGTTGCCCAAGTGGA | 58513 |
rs781606449 | snp | C/T | 1.6759e-05 | 0.00289469 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16442232 | AATCTGTAAATGAAA[C/T]CACAGATATTGGTCA | 58513 |
rs781632160 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424724 | GGAGTGCAGTGGCGC[A/G]CTCTCAGCTCACTGC | 58513 |
rs781674469 | snp | A/C | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16392398 | TCAGTGGCAGAGCCA[A/C]GGAATGGGTCACTTT | 58513 |
rs781706886 | in-del | -/AAG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428596 | AAGAAAAGAAAAGAA[-/AAG]AAAAAAGAAAAGAAA | 58513 |
rs781714439 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456611 | TGCAGTGAGCCAAGA[C/T]GATGCCATTGCACTC | 58513 |
rs781727902 | in-del | -/GAGT | 2.85939e-05 | 0.00378102 | intron-variant | EPS15L1 | GRCh38.p7 | 19:16428812 | GGAAGGACTGGGTGA[-/GAGT]GAGACCACCTGCCGG | 58513 |
rs781743683 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467090 | ATCCAAACAAACATC[G/T]AAGGACCTAAACATT | 58513 |
rs796114219 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16371750 | GACACCCACACAGCC[A/G]TTTCCTGCACTTAAA | 58513 |
rs796122202 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16362315 | CATGGCAACACATTT[A/G]TTAACATACTAATTT | 58513 |
rs796132357 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412792 | AGCAGTGGCATCTGG[G/T]GCTGGGGTCGCGGCC | 58513 |
rs796135216 | in-del | -/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16422980 | AAAAAAGGGGGGGGG[-/G]ATTTCTCAAAGAGTT | 58513 |
rs796196586 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16440740 | TCCCGTGTTAAGTTT[A/G]ACAGCCGTGCTCATG | 58513 |
rs796205217 | in-del | -/GT | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16367985 | TGAGAGAGAGAGAGA[-/GT]GTGTGTGTGTGTGTG | 58513 |
rs796216030 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | EPS15L1 | GRCh38.p7 | 19:16361596 | GGCTCTTTTTTTTTT[A/T]ATTGAGAAACTGTTT | 58513 |
rs796242279 | in-del | -/A | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16419456 | GTGAGTCTCTGTCTC[-/A]AAAAAAAAAAAATAA | 58513 |
rs796260100 | snp | G/T | | | downstream-variant-500B | EPS15L1 | GRCh38.p7 | 19:16355134 | CTTAAAAAAAAATTT[G/T]TTTTAAAAGTAAAAA | 58513 |
rs796298423 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16365355 | TAACTGAGTTAAAAC[C/G]AAGTCAAAGGATCAA | 58513 |
rs796322362 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16456224 | AAACAAAAAACCCTC[C/T]TGAAAAAGGGTCCAC | 58513 |
rs796323031 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16358314 | GCACTTAGGAGGCAC[A/G]CTGGGCTGTGAGGCC | 58513 |
rs796356261 | in-del | -/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16398995 | CATTTATTTATAAGG[-/T]TTTTTTTTTTCAGTG | 58513 |
rs796363490 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366728 | ACGTGTGAGGTCAGC[C/T]GAGTGCCCGGTCCAG | 58513 |
rs796367706 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16376919 | GCCCACAGGACGGGG[C/T]GAGGGCGGGCAGGCA | 58513 |
rs796452266 | in-del | -/TGTGTGTGTGTG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16375467 | GTGATTATGCATATA[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 58513 |
rs796479020 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16462359 | TGGGAGACCAGGTTA[C/T]CAGAATCAGGGAAGT | 58513 |
rs796489656 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16467282 | GGGTCCCGAGTGGCC[A/G]GGATTACAGGCGTCC | 58513 |
rs796494743 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366013 | CCTTCCTGGTTTGCA[A/G]GAAACAGCAATGTTA | 58513 |
rs796499635 | in-del | -/GC | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472434 | TGTGTGTGTGTGTGT[-/GC]GCGCTAATTTGGGGG | 58513 |
rs796504063 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16364495 | CCGGGGCTGCAGAGA[A/G]CAGGGTGATCTGGCC | 58513 |
rs796588861 | snp | G/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16414717 | TTTTGGTTTTGTTTT[G/T]TTTTTTTTTTGAGAC | 58513 |
rs796595253 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16453020 | TTAGTCAGGATGGCC[C/T]CGATCTCCTGACCTC | 58513 |
rs796623648 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16445770 | CCTGGGGCCAAGCCC[A/G]AGGCAACAGCAGAGA | 58513 |
rs796625907 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16366015 | TTCCTGGTTTGCAGG[A/G]AACAGCAATGTTACT | 58513 |
rs796653374 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16464250 | AAAGCTTGTAGTATC[A/G]AGAGCTGGGACTCCT | 58513 |
rs796685442 | in-del | -/GGGGG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16412714 | GGTGCAGCGGGGGGT[-/GGGGG]GGGGGGGGGTGTCAG | 58513 |
rs796689415 | in-del | -/C | | | upstream-variant-2KB | EPS15L1 | GRCh38.p7 | 19:16472129 | GGGCGGGGCCGCCCA[-/C]ACGCAGCCTGGAGGG | 58513 |
rs796704355 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16424940 | TGCTGGGATTACAGG[A/C]GTGAGCCACCGCACC | 58513 |
rs796742552 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369057 | AAATTCATCACTGCT[C/T]GGGGACTTGTCTTGA | 58513 |
rs796830796 | in-del | -/TA | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16369708 | GTGTGTGTGTGTGTG[-/TA]GGGTGGGGTATGTGA | 58513 |
rs796848245 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16363676 | AATGAGAAGGAGGGC[A/G]CCAAACAAGGTGACA | 58513 |
rs796871907 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16451715 | TTGTATTTTTTAGTA[C/G]AGACAGGGTTTCACC | 58513 |
rs796895075 | in-del | -/GCAC | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16460990 | ATATAAAATTGAAAA[-/GCAC]GTCCTCTTCAGATTA | 58513 |
rs796901740 | in-del | A/TG | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16436388 | TTTTTTCTTCTTTCT[A/TG]ACGCAGTAGCTTATC | 58513 |
rs796931465 | snp | A/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16391062 | ACTGCATCTCGATAA[A/G]ACTATTGTAAAGTCA | 58513 |
rs796936771 | snp | C/G | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16457702 | TTAAGAGCAAAAGCA[C/G]ATGAAGCCTCTGAGC | 58513 |
rs797012378 | snp | C/T | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16411523 | GATGGTTAATCAACA[C/T]GGTGATTATGCGAAA | 58513 |
rs797021470 | snp | A/C | | | intron-variant | EPS15L1 | GRCh38.p7 | 19:16400350 | TCAAAAAAAAAAAAA[A/C]AAAAACAAAAAAAAA | 58513 |