SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs77269088 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235681186 | ATATGAACTGAAGTT[C/T]TGAAGAACTGGCAGA | 1130 |
rs77282963 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | LYST | GRCh38.p7 | 1:235790168 | TTTCTCAGGTCACTA[C/T]GTATATTTATTCATT | 1130 |
rs77300728 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235771609 | TTATCTTTTTTTTTT[A/G]GATCTGAAAGTATAT | 1130 |
rs77322448 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235745624 | ACCTGCACATAAATG[C/T]TTACAGAAGCTTTAT | 1130 |
rs77341658 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235807562 | TTGATTTAACATCAA[C/T]AATAGTTTTAAAGTA | 1130 |
rs77366316 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235778884 | TTTCTTTTTTTTTTT[G/T]AGACAGAGTTTGACT | 1130 |
rs77395892 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661645 | AGTCTGGAAGTTACA[A/G]AAGTAGTACTGTAAA | 1130 |
rs77411322 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | LYST | GRCh38.p7 | 1:235769601 | AAGCAGATATTTATC[A/G]ATGCCTTTTATCTGT | 1130 |
rs77414932 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235745451 | GGATGTAAAAAAACT[A/T]GGACCACTCATACAC | 1130 |
rs77442892 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235844671 | TACATACACCTGGAA[A/G]CAAGATTTTTAAACC | 1130 |
rs77536847 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235869482 | GTCTCAAAAAAAAAA[A/T]TAATAATTAAAAAAG | 1130 |
rs77537095 | snp | G/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235782195 | CTTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTCG | 1130 |
rs77550273 | snp | C/T | 0.084364 | 0.187256 | intron-variant | LYST | GRCh38.p7 | 1:235729538 | AAACACTTTAAATAA[C/T]CTAAGAATCAAATAA | 1130 |
rs77565039 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858392 | TAGTAGTTTTTATTA[A/T]TATTAATATTGTTAT | 1130 |
rs77585326 | snp | A/T | 0.444444 | 0.157135 | intron-variant | LYST | GRCh38.p7 | 1:235774240 | AACAAACAGCACTCA[A/T]TTTTTATGTTTTAAA | 1130 |
rs77611757 | snp | A/C | 0.0577344 | 0.159793 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662255 | AGAAACAGAATGTGT[A/C]TGAAATCCAAGATAC | 1130 |
rs77628694 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235812503 | CAGAGTGAGACTCTG[A/C]CTAAAAAAAAAAAAA | 1130 |
rs77641278 | snp | C/T | 0.0107246 | 0.0724382 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662215 | CAATATCTAGCGTTA[C/T]AGATTTTAAGTAAAA | 1130 |
rs77665259 | snp | A/G | 0.135484 | 0.22223 | intron-variant | LYST | GRCh38.p7 | 1:235849637 | GGACTCCTCTAGAAA[A/G]CTCACGGAACTGATA | 1130 |
rs77693204 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | LYST | GRCh38.p7 | 1:235797522 | CATTCAATGGGGGAG[A/G]GACAGTCTCTTCAAC | 1130 |
rs77740574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235699081 | TTATATCATAGCATA[C/T]TTATGATCATTATTC | 1130 |
rs77771534 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235695063 | CTAGAATGTCTATGT[A/G]GACTGTTCCTTGCTG | 1130 |
rs77776101 | snp | C/T | 0.132751 | 0.2208 | intron-variant | LYST | GRCh38.p7 | 1:235848191 | AAGCACTCTCTCAGA[C/T]CACAGCGGCATAAAA | 1130 |
rs77794257 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738016 | AGTATACGCTCAAGG[A/G]TCAGCTTATTCACAG | 1130 |
rs77797229 | snp | A/G | 0.084364 | 0.187256 | intron-variant | LYST | GRCh38.p7 | 1:235807024 | TAAAAAGAAAAGATT[A/G]CCTGTCCCACATTAA | 1130 |
rs77801066 | in-del | -/AAACTA | | | intron-variant | LYST | GRCh38.p7 | 1:235802218 | AAAAAAAAAAAAAAA[-/AAACTA]GCAGTACTGGGACAC | 1130 |
rs77821973 | snp | A/G | 0.116138 | 0.211142 | intron-variant | LYST | GRCh38.p7 | 1:235710864 | ACATCCAGGGCTGCC[A/G]TGCTGTGGGGAAGCC | 1130 |
rs77848653 | snp | A/G | 0.00155072 | 0.0278021 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809434 | CTGAGGCCTCGGGAG[A/G]AACTCCATCTCTTAA | 1130 |
rs77866548 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYST | GRCh38.p7 | 1:235706298 | CATAAGATTTTCACT[C/T]AGGAGTTACCCTCCC | 1130 |
rs77905667 | snp | A/C | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235837626 | TGAGACCCTGTTTCA[A/C]AAAAAAAAAAAAAAG | 1130 |
rs77919900 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235721202 | TAAAAGAAAAAAAAA[A/T]AAGGAAAAAAGAAGA | 1130 |
rs77934748 | snp | C/T | 0.084364 | 0.187256 | intron-variant | LYST | GRCh38.p7 | 1:235804159 | AGGATAGGTAAATCA[C/T]CACCATCCCTGAATT | 1130 |
rs77961942 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235694836 | ACAAGAGGCATCATC[C/T]TTTTTTTTTTCTTTC | 1130 |
rs78003821 | snp | G/T | 0.067446 | 0.170804 | intron-variant | LYST | GRCh38.p7 | 1:235806876 | GCATGTGGGATATAC[G/T]AACCACTACCTAATT | 1130 |
rs78106418 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235882551 | TGGTGAGGAGACTCT[C/T]GCAGTAGCCCAAGAG | 1130 |
rs78155850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697669 | GAAATCAAGACCACA[C/T]GTAGCACAGGAAACC | 1130 |
rs78161080 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827755 | AAATACCACCACAGG[A/G]AAAAAATATTTAACT | 1130 |
rs78171965 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827551 | TCTTAAATGATAAAA[A/T]ATCATTCAATTAATT | 1130 |
rs78172154 | snp | A/G | 0.000296545 | 0.0121731 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806619 | AATGTCTATCCCATC[A/G]ATATCTGGAACTGAG | 1130 |
rs78202197 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235663249 | TAATTCTAACATAGT[C/T]ACTCTGCTGACAAGT | 1130 |
rs78219692 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235669361 | ATTCAAAGGAAAACC[A/C]TAACTTTCCAGGCCT | 1130 |
rs78222301 | snp | C/T | 0.084364 | 0.187256 | intron-variant | LYST | GRCh38.p7 | 1:235723243 | GTTACGTTTGAGATG[C/T]CAATTAGTGACTTCT | 1130 |
rs78330092 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | LYST | GRCh38.p7 | 1:235823579 | AGGCTTGCCATGTCA[C/T]GGCCTCTGCCCTTCA | 1130 |
rs78336614 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235791559 | CTTTGATAAGTCAGG[A/G]CCTACCACCACTAAG | 1130 |
rs78352777 | snp | A/T | 5.08186e-05 | 0.00504051 | intron-variant | LYST | GRCh38.p7 | 1:235663095 | TGTAAAAAAAAAAAA[A/T]TTCCCATTTGTACAT | 1130 |
rs78357932 | snp | A/C | 0.115788 | 0.21092 | intron-variant | LYST | GRCh38.p7 | 1:235725459 | AAAATAACAAAATAA[A/C]AATAAAGAGGATTAA | 1130 |
rs78363909 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235663704 | TGGTCTTGTCAAATA[A/T]GAAAGGAAAAAATAC | 1130 |
rs78366693 | snp | G/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235782197 | TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTCGCT | 1130 |
rs78369033 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235869483 | TCTCAAAAAAAAAAA[A/T]AATAATTAAAAAAGC | 1130 |
rs78415446 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235684029 | GGTGGAAAAAAAATC[C/T]TATAAAAATTAGCTG | 1130 |
rs78425567 | snp | A/G | 0.000743218 | 0.0192628 | intron-variant | LYST | GRCh38.p7 | 1:235724000 | GAGCACTTAAACAAT[A/G]TATATCAATTAATAA | 1130 |
rs78459771 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | LYST | GRCh38.p7 | 1:235666908 | AGGTAGGGGTTTCTC[A/G]CTGTAACCCATAGCT | 1130 |
rs78462166 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | LYST | GRCh38.p7 | 1:235701742 | GAAAACAAAAAATAT[A/G]GTTTTCTATTATGAA | 1130 |
rs78462768 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | LYST | GRCh38.p7 | 1:235700907 | TATAGACAAATAAAT[A/G]AACAAATACATATAC | 1130 |
rs78477997 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | LYST | GRCh38.p7 | 1:235808050 | GCCAATAATATTCTA[C/T]CAAGGAAATATAAAG | 1130 |
rs78568005 | snp | A/C/T | 0.0150606 | 0.0854603 | intron-variant | LYST | GRCh38.p7 | 1:235863150 | GTAATCCAGGCACAG[A/C/T]TGGGGGCCGAGGAGG | 1130 |
rs78570436 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235695628 | ACTTTACAGTACTCT[A/T]ATTTTTTTTTTTTTT | 1130 |
rs78598087 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235746043 | GTAAAGGGTACACAG[C/G]GTCTCTCTCTGTATT | 1130 |
rs78611805 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853175 | GTTTCCACATTGTAC[A/C]TTTATACCAAAAAGT | 1130 |
rs78622617 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235869471 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAATAAT | 1130 |
rs78672331 | snp | A/G | 0.0191827 | 0.0960385 | intron-variant | LYST | GRCh38.p7 | 1:235830190 | AGTTAACTATCATAT[A/G]TTGATGAAAGTAAGT | 1130 |
rs78699311 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | LYST | GRCh38.p7 | 1:235764260 | CACTGTGCTTTCCAC[A/G]TGGCATGATATAATC | 1130 |
rs78713790 | snp | A/G | 0.077417 | 0.180873 | intron-variant | LYST | GRCh38.p7 | 1:235754649 | GAACTATAAAGGATG[A/G]AGTTATATTAGAAAG | 1130 |
rs78772920 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | LYST | GRCh38.p7 | 1:235880830 | ATTTTTTCCTTTAAA[G/T]AATTCCATTTAGCGG | 1130 |
rs78782064 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235668861 | ACCAAAGTCAACTCT[G/T]TAAGATCTTTTCCCT | 1130 |
rs78819064 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235824310 | TGAAATTTTAAAAAG[C/T]AGTATTTATAACACA | 1130 |
rs78823696 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | LYST | GRCh38.p7 | 1:235665250 | AAATATGAGTTATGA[C/T]TGAAAATACTTGGAA | 1130 |
rs78845350 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | LYST | GRCh38.p7 | 1:235767377 | GGAACACTGAGTCTA[C/T]AGAAGAAAACACAAA | 1130 |
rs78857731 | in-del | -/TATTAA | 0.470272 | 0.118238 | intron-variant | LYST | GRCh38.p7 | 1:235858387 | ATGAATAGTAGTTTT[-/TATTAA]TATTAATATTGTTAT | 1130 |
rs78863250 | snp | A/G | 0.084364 | 0.187256 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738111 | ATGGCCTGTGCCATC[A/G]GTATCTTAATGAAGG | 1130 |
rs78871711 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235869472 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAATAATA | 1130 |
rs78874267 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | LYST | GRCh38.p7 | 1:235874326 | AATGTTCAAGGCTTT[A/G]GAATGAAAGACATTC | 1130 |
rs78879797 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235771940 | TTTTTTTTTTTTTTT[G/T]GGCCAGGCATGGGGG | 1130 |
rs78884047 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | LYST | GRCh38.p7 | 1:235820097 | TACCAACAAGGTGCC[A/G]GGCACTGGCCCTTTT | 1130 |
rs78968968 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235834954 | GAGTTTCACCCTTTC[A/C/G]CCCAGGCTTGAGTGC | 1130 |
rs79008260 | snp | C/T | 0.146985 | 0.227789 | intron-variant | LYST | GRCh38.p7 | 1:235857786 | ACACACACACACACA[C/T]ATATATATAAAATTT | 1130 |
rs79017910 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235823952 | AGAGGTGCTGGGCCA[C/T]AGTAGGTACTTAATG | 1130 |
rs79056748 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | LYST | GRCh38.p7 | 1:235742925 | GAGAGACTACATTTA[C/T]GTAACTTTTATTAAA | 1130 |
rs79070269 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | LYST | GRCh38.p7 | 1:235882507 | CTGAAGAGAGGATTG[G/T]AGGTGAAAGGGACTA | 1130 |
rs79083223 | snp | C/G | 0.039522 | 0.134904 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868604 | ACTTTAGATGATAAT[C/G]GTATACAATTGGCCC | 1130 |
rs79086262 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235750026 | AAGAAACAGCAGGGG[G/T]AGTAAAGGTATACTT | 1130 |
rs79137670 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845316 | TACAGGGGTAGAGAA[A/T]GCAGCAGAAAGGCCC | 1130 |
rs79176214 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | LYST | GRCh38.p7 | 1:235751809 | CAACTACTAACTACA[A/T]GGGGGAATCACTTTT | 1130 |
rs79195959 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235736427 | TGAGGATATAGATAG[A/C]CAAAGGAGAGAGAGG | 1130 |
rs79208127 | snp | C/G | 0.0836354 | 0.186609 | intron-variant | LYST | GRCh38.p7 | 1:235795878 | GAGATAATTTGGGGA[C/G]AGAAGAAACTTTAAG | 1130 |
rs79266423 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235721201 | CTAAAAGAAAAAAAA[A/T]TAAGGAAAAAAGAAG | 1130 |
rs79420212 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845314 | ATTACAGGGGTAGAG[A/G]ATGCAGCAGAAAGGC | 1130 |
rs79423578 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235695630 | TTTACAGTACTCTAA[A/T]TTTTTTTTTTTTTTT | 1130 |
rs79426009 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | LYST | GRCh38.p7 | 1:235795553 | TCTAAGGTATGCAAA[C/T]TGCCATGTAGGGTAA | 1130 |
rs79429343 | snp | C/T | 0.030278 | 0.119257 | intron-variant | LYST | GRCh38.p7 | 1:235836379 | CAGGTCATGTTAATT[C/T]GATGAAAAAGTAAAA | 1130 |
rs79439395 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235780798 | ATCTAATTCATAACT[A/G]TACATTACAATAAAT | 1130 |
rs79463464 | snp | C/T | 0.137187 | 0.223099 | intron-variant | LYST | GRCh38.p7 | 1:235696743 | AAACCCATGACTATA[C/T]CTTCTGAGATGGTAG | 1130 |
rs79542484 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | LYST | GRCh38.p7 | 1:235732723 | ATTGAATATTTTCCC[A/G]TGTGTTTGGTAATTC | 1130 |
rs79563427 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | LYST | GRCh38.p7 | 1:235780664 | TCAAGGAAAAGGAGA[C/T]ATAAATATAAAGCCT | 1130 |
rs79573302 | snp | C/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235864048 | GTCTTCAGCAAGAAT[C/G]CCGTTAGGTCGGCTT | 1130 |
rs79577351 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | LYST | GRCh38.p7 | 1:235748687 | AACTGCTGAGCAGAA[A/G]AATGGTAAACCTGAA | 1130 |
rs79622794 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235694835 | CACAAGAGGCATCAT[C/T]TTTTTTTTTTTCTTT | 1130 |
rs79625289 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827753 | AAAAATACCACCACA[A/G]GAAAAAAATATTTAA | 1130 |
rs79640717 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235730001 | ACATTTTTTGTGTGT[G/T]CTCTATTTATTTTTG | 1130 |
rs79656514 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235780273 | GCCCGGTGTGGTGAT[A/G]CATGACCACAGGCCC | 1130 |
rs79671675 | snp | C/T | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854459 | TCAGTAAATGGCCTC[C/T]ACCCAGTGACTGAGG | 1130 |
rs79679095 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235729346 | TGGTTAAATATAAAT[G/T]TGCATATCATGAAGA | 1130 |
rs79746891 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235793138 | TAGACAATAATTGAA[C/G]AGTATAGTGGATAAT | 1130 |
rs79755770 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235691433 | GTTCTTTCTACTATA[A/C/G]ATGATGTCTGAATAA | 1130 |
rs79760880 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235802193 | AGCAAGACTCCATTT[A/C]AAAAAAAAAAAAAAA | 1130 |
rs79768212 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235820102 | CAAGGTGCCAGGCAC[-/CT]TGGCCCTTTTCATAA | 1130 |
rs79779542 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235694177 | ACCATGCCCGGCTGA[A/T]TTTTTTTTTGTATTT | 1130 |
rs79801442 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | LYST | GRCh38.p7 | 1:235857788 | ACACACACACACATA[C/T]ATATATAAAATTTCA | 1130 |
rs79862826 | snp | C/T | 0.132751 | 0.2208 | intron-variant | LYST | GRCh38.p7 | 1:235845808 | TGGGAATCTCACCCC[C/T]AATTCCCCACAGCAG | 1130 |
rs79863292 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | LYST | GRCh38.p7 | 1:235855254 | TAACACAGTACCACA[A/G]ATACAAGAGTTCAAT | 1130 |
rs79866370 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235746294 | ATTACTTCTCTTTCA[G/T]TTTAAAATCTGAGGA | 1130 |
rs79915855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823650 | GCAAAGTTCAGCCTT[C/T]GCTGTAACTTCACTA | 1130 |
rs79974781 | snp | C/T | 0.030665 | 0.119967 | intron-variant | LYST | GRCh38.p7 | 1:235765342 | TTATCCTGTCTCTCA[C/T]GGACTACTATAATTG | 1130 |
rs80032082 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235701213 | TGGTACCATGTTCCC[A/T]CTGCGAGCAGACATA | 1130 |
rs80078938 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235872573 | GAATGAAGGTCTTAT[G/T]ACCTAGAATCATCCA | 1130 |
rs80116017 | in-del | -/A | 0.0524604 | 0.153226 | intron-variant | LYST | GRCh38.p7 | 1:235717916 | TTTTCACTCTGGAGT[-/A]GAAGTGGCGTGATCT | 1130 |
rs80130899 | snp | A/T | 0.0637235 | 0.166737 | intron-variant | LYST | GRCh38.p7 | 1:235796814 | TTTCTGTTCATTACA[A/T]ATCACTCAGTCTGTG | 1130 |
rs80278617 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | LYST | GRCh38.p7 | 1:235744607 | ATATTAGAAAAGTGG[A/G]AAAAAAAAAATGCTG | 1130 |
rs80324250 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235769194 | AGTCTTAAGTTGCCA[C/T]GTGGAGGATAAGTAG | 1130 |
rs80338642 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830299 | AGGAGACGCACATGG[-/G]CAACCCTTGGACAGT | 1130 |
rs80338643 | snp | C/T | | | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830270 | TACCTTGTCCATGGT[C/T]GAGGATTTCTATTAC | 1130 |
rs80338644 | in-del | -/G | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809351 | AAAAGTGAAATCAGA[-/G]CAACTTCATCATTCG | 1130 |
rs80338645 | snp | C/T | | | stop-gained, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809278 | TTTATGCATCATCAC[C/T]GAGATCTCTCAGGTC | 1130 |
rs80338646 | in-del | -/A | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808915 | CCAAAAATTAAAAAA[-/A]GCAGCTTGTAATATT | 1130 |
rs80338647 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806723 | GTAAGTCAAATAATC[-/G]AATTAAATTGCTTAA | 1130 |
rs80338648 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806682 | AAGTCATTCTCTAAA[-/A]GCATTTGAAACTCTG | 1130 |
rs80338649 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806513 | AGTCTCAGCAAATTT[-/T]ATGCTGGCCTCAAAG | 1130 |
rs80338650 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806062 | GAAAACCAGGATTTA[-/AA]CAGAATTTCTCAACC | 1130 |
rs80338651 | snp | C/T | | | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806051 | TTAAACAGAATTTCT[C/T]AACCTAAGAGAACTA | 1130 |
rs80338652 | snp | C/T | 4.9525e-05 | 0.00497595 | LYST | 1 | allele_origin=T(germline)/C(germline) | 1:235805826 | TCACTTCAAAGTATA[C/T]GACTTTTGGAAGCCC | 1130 |
rs80338653 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804624 | TGAAATGAGGGACCA[-/A]TCTTTCCCAGTCAAA | 1130 |
rs80338654 | snp | C/G | | | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793567 | TATCTTTGATGAGTT[C/G]AAGAACATGTTCAGA | 1130 |
rs80338655 | snp | A/C | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791881 | CATCTTGGCACATAG[A/C]CCCAGTCCACCTGCC | 1130 |
rs80338656 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791968 | GTAAGGCCATGGGTT[-/T]ATTGAGAAGAGCACG | 1130 |
rs80338657 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788701 | CCACTCTTATCTTTC[A/G]GTATTGATTATCCTC | 1130 |
rs80338658 | snp | A/C/T | 6.87144e-05 | 0.0058611 | LYST | 1 | allele_origin=T(germline)/A(unknown) | 1:235781018 | GGCCTTTTATCTGTA[A/C/T]GCTTGTGGACCCAAC | 1130 |
rs80338659 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777206 | ACCCAACTCTCTCAA[-/A]GACCCTTCAGCTCAA | 1130 |
rs80338660 | snp | A/C/T | 0.00142342 | 0.0266402 | LYST | 1 | allele_origin=A(unknown)/C(germline) | 1:235766122 | TCCTACTAATACTTA[A/C/T]GTTTGTCACAATCCC | 1130 |
rs80338661 | in-del | -/CTATTAG | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755641 | AAATTTTTTGTTTAG[-/CTATTAG]ATGCATATTTTGCTA | 1130 |
rs80338662 | in-del | -/T | | | frameshift-variant, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752077 | TCCTCAGGCTCACAA[-/T]ATTTTAGGGTTATTG | 1130 |
rs80338663 | snp | A/G | | | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734590 | GAATTGACTGAAGAA[A/G]AGCTAGGCACAGCAG | 1130 |
rs80338664 | snp | A/G | | | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733859 | GAATAAAGCTGCTTG[A/G]CAGAAAACAGTTAAC | 1130 |
rs80338665 | in-del | -/GTAAATGTGGAATGTATTTTGTGGAAGATAATGCTTCTGATACAGTTGAAAGTTCG | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728076 | AATTACTTTCTGCAG[lengthTooLong]GTGAGTAGAGGCTTA | 1130 |
rs80338666 | in-del | -/TTCTTTCAGT | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724114 | ATTAAAGAAGTTCAC[-/TTCTTTCAGT]AAGCGTTGGTGGCAA | 1130 |
rs80338667 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716749 | CTATAGCTGTTCAGT[-/A]TAAAGAAAAAGAAGA | 1130 |
rs80338668 | in-del | -/T | | | frameshift-variant | LYST | GRCh38.p7 | 1:235712089 | TTATCCCAGAGTTTT[-/T]CTATCTTCCAGAGTT | 1130 |
rs80338669 | snp | A/G | 1.64898e-05 | 0.00287135 | LYST | 1 | allele_origin=G(unknown)/A(germline) | 1:235709107 | CTGTTCAAGCGATCA[A/G]TGTTTTTCATCCTGC | 1130 |
rs80338670 | in-del | -/A | | | frameshift-variant | LYST | GRCh38.p7 | 1:235697252 | TTTGTCATGGATAAA[-/A]GGCTTGAAATGGGGG | 1130 |
rs80351112 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868189 | TTATCTTTTTTTTTT[G/T]GAGACAGATTCTCGC | 1130 |
rs111286397 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235730567 | TATATACATATTTAT[A/G]TGTGTGTGTGTGTGT | 1130 |
rs111292479 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235878971 | GTCTGGGCTGTTAGA[A/G]TACCCATCACCTGAA | 1130 |
rs111310823 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235774087 | TTTAGCAATCATTAA[A/T]TTCAAAGGAAAGCTA | 1130 |
rs111312137 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235771918 | AGGTTTTTTAGTTTG[G/T]TTTTTTTTTTTTTTT | 1130 |
rs111315307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235783468 | GGGAACATCACACAC[C/T]GGGGCCTGTCGGCGG | 1130 |
rs111321906 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235777344 | TTCAGTAATGACAAC[A/G]AGTTTAAAATGCAAG | 1130 |
rs111336926 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235680980 | CCAACAAACATTGTT[C/G]AGTGTCCCCTACTGT | 1130 |
rs111358502 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235663192 | CAGTGGCGCAGAGAG[A/G]CATAAACTAAATGAC | 1130 |
rs111364330 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235666753 | AGACAATATTTTCCA[C/T]GAGTAGGCTACATTT | 1130 |
rs111365174 | snp | C/T | 0.0107286 | 0.0724924 | intron-variant | LYST | GRCh38.p7 | 1:235693111 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTTGCT | 1130 |
rs111371207 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235715450 | TTCTCTCCTTCTCTA[C/G]TACCCCTTTGAGGCC | 1130 |
rs111371650 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235672264 | AAAATAAATTTAGGA[A/G]TCATTAGGGAATAAC | 1130 |
rs111415763 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | LYST | GRCh38.p7 | 1:235858429 | CACTATTAATCTTGG[C/T]TATCCACCCATCATT | 1130 |
rs111424523 | in-del | -/CTA | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235666648 | CACATGCCCAATGTT[-/CTA]CTAAGTTTTCCCATT | 1130 |
rs111446451 | snp | A/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235882070 | CATACACACACACAC[A/T]CTTTCTTTCACACAC | 1130 |
rs111450686 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235864926 | AAAGTGAGATCCTGA[C/G]TCAAAACTAAAAATA | 1130 |
rs111456284 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235744379 | CATACAATTCCAAAT[C/T]AAATATTTAATGGAC | 1130 |
rs111463684 | snp | C/T | 0.000330017 | 0.0128413 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806436 | AGCCACACAGAGGAA[C/T]AGGTTTATTGTGTTG | 1130 |
rs111464279 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235774025 | AATATAAGATGCATT[A/C]GTAATTGGTTAATCA | 1130 |
rs111474890 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235820382 | TTTTCTTTCTTTTTT[A/T]TTTTTGAGACAGGGT | 1130 |
rs111498729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235858024 | ATTTACTGAGAATTT[C/T]GTCGTATGACTATCT | 1130 |
rs111505262 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235727344 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 1130 |
rs111527524 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235721654 | GGAAATGTACTGGTA[A/G]TTGTGGAATAGGCAA | 1130 |
rs111529565 | in-del | -/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235762903 | TAAAAAGGATAAAAC[-/G]AAAATATAACTTTAA | 1130 |
rs111544393 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | LYST | GRCh38.p7 | 1:235699670 | CTGTCTTCCACAAGG[G/T]TTGAACTAATTTACA | 1130 |
rs111557197 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750938 | CCCTACTATTTTACA[A/T]TCTCTGCAGGGGCAG | 1130 |
rs111592940 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235872652 | TTGGGCAGAAAGAGT[A/G]GCTCATACCTGTAAT | 1130 |
rs111604388 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235823034 | ATGCCAGAACTGCCA[A/G]CTCAACAGAATCATG | 1130 |
rs111627430 | snp | G/T | 0.0584853 | 0.160693 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868399 | AACTTAACCTGTTTC[G/T]TCATTTTACCTAAAG | 1130 |
rs111633663 | snp | C/T | 0.000164913 | 0.00907906 | intron-variant | LYST | GRCh38.p7 | 1:235677067 | CACCAGCCAGCCCTG[C/T]GCTTTGGGTTGGAGC | 1130 |
rs111659738 | snp | A/G | 0.5 | 0 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808988 | AAGGATATTCAATAT[A/G]TGCTGCTGAAAATTT | 1130 |
rs111663040 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235830548 | TACTGGAAATTGGTA[C/T]TTAACCCTATAATAT | 1130 |
rs111680478 | in-del | -/T | 0.163236 | 0.234461 | intron-variant | LYST | GRCh38.p7 | 1:235680430 | CAACTACTTTTTAAA[-/T]TTTTTTTTTTTTGTG | 1130 |
rs111682199 | snp | A/C | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235786303 | AGATTTGTAAGTTAA[A/C]GTATAGTAAATTTTT | 1130 |
rs111688389 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852723 | TTAATAAATTATTTT[A/C]AAATGAGAATCCATT | 1130 |
rs111688783 | snp | C/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235843941 | CTAATTTTCTCAATT[C/G]AATAGTATTAGAGAA | 1130 |
rs111692985 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235851177 | ATGTAAGTATGTATG[C/T]ATATGTGTGTGTATA | 1130 |
rs111699537 | snp | C/T | 0.177503 | 0.239258 | intron-variant | LYST | GRCh38.p7 | 1:235692193 | CAAAAATTAGCCAAG[C/T]GTGGTGGCACATGCC | 1130 |
rs111720904 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718496 | CGAACTCCTGACGTC[A/C]GGTGATCTGCCTGCC | 1130 |
rs111722949 | snp | C/T | 0.000658913 | 0.018139 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791905 | CAAGATGAAAGCAGC[C/T]GATGGGGAAAACTCT | 1130 |
rs111745565 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | LYST | GRCh38.p7 | 1:235700300 | TGAACAAGCAACCTA[C/T]AGAATGGGAGAAAAT | 1130 |
rs111763883 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235778623 | TGAACTTCTGACCTC[A/G]TGATCTGCCCGCCTC | 1130 |
rs111764031 | snp | A/C/T | 0.00412128 | 0.045208 | intron-variant | LYST | GRCh38.p7 | 1:235757274 | CATATCTAGTATTTG[A/C/T]CCTTACTTTAATAAC | 1130 |
rs111768118 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235723745 | GAGCAGAGAAATGGT[A/G]GCCGAAGGGATTAGA | 1130 |
rs111770759 | snp | A/G | 0.000395387 | 0.0140548 | synonymous-codon | LYST | GRCh38.p7 | 1:235662964 | TGCATAGCTGCTAAG[A/G]AAGGAATAGAACATT | 1130 |
rs111789893 | in-del | -/CT | 0.0818113 | 0.184966 | intron-variant | LYST | GRCh38.p7 | 1:235726809 | ACAGATGGACTCAGA[-/CT]CTTCTGTCACCTCAT | 1130 |
rs111806240 | snp | C/T | 0.000181292 | 0.0095191 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810342 | GAGAGCTGTGTCTTT[C/T]TTGCATCTCTTACAG | 1130 |
rs111866292 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235845117 | CCCTCTGAAGGAAGC[A/G]GATTGCTCCTGCAGG | 1130 |
rs111868702 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | LYST | GRCh38.p7 | 1:235834649 | CTAGGCACTTGAAGA[C/T]AAACCAGGCAGAAAA | 1130 |
rs111884548 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235819888 | CCTGACCTCGTGATC[C/T]GCCAGCCTCAGCCTC | 1130 |
rs111889116 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235824818 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 1130 |
rs111899529 | in-del | -/A | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235744607 | GTGGAAAAAAAAAAA[-/A]TGCTGGGGACGATGG | 1130 |
rs111904968 | in-del | -/AAAAC | 0.0872718 | 0.189788 | intron-variant | LYST | GRCh38.p7 | 1:235769017 | ATTACAGTGTGATTT[-/AAAAC]AAAACAAAACAAAAA | 1130 |
rs111936764 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235795623 | TTAGGGTGTTTGGGA[A/G]GCCCCTAATCATCCA | 1130 |
rs111943484 | in-del | -/A | 0.0984431 | 0.198823 | intron-variant | LYST | GRCh38.p7 | 1:235702051 | TCTTTAAGGTCCTTT[-/A]CAACGTCTTTCCCTT | 1130 |
rs111957842 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235704769 | AGATCCCACTTGTCA[A/G]TTGTTGCTCTTGTTG | 1130 |
rs111965995 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | LYST | GRCh38.p7 | 1:235736968 | GAACCATGTAGACAT[G/T]TCACATGATTAAAAA | 1130 |
rs111967867 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738824 | GCACCCAATTTCCAC[A/C]ATGATTGGTGGAATA | 1130 |
rs111975307 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | LYST | GRCh38.p7 | 1:235791155 | AGGTGTGATTGCTGG[C/T]GCCTGAATCCCAGCT | 1130 |
rs111990037 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689783 | CCTTAAATATATACA[A/T]TTTTATTTGTCAATT | 1130 |
rs112010120 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | LYST | GRCh38.p7 | 1:235755233 | TCTCTACTAAAGATA[C/T]AAAAAACTAGCCGGG | 1130 |
rs112030285 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | LYST | GRCh38.p7 | 1:235841978 | TTACTGGTTGGCTAC[C/T]AGCTTAGCAGAGGTG | 1130 |
rs112045100 | in-del | -/G | 0.456419 | 0.17902 | intron-variant | LYST | GRCh38.p7 | 1:235835100 | TTTTGTATTTTTAAT[-/G]GGGGGGGGGTTTCGC | 1130 |
rs112061639 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866191 | CATCAGAAGCGAAGG[A/G]GCATCTCAGTCAGGC | 1130 |
rs112066543 | snp | A/G/T | 0.0618563 | 0.164627 | intron-variant | LYST | GRCh38.p7 | 1:235697974 | TGGCTGCCCACGAAC[A/G/T]GTAATGAAAAGGTTT | 1130 |
rs112082207 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826607 | TGAAAAAAAAGGCAT[A/G]ACAAAACTTTCTAAG | 1130 |
rs112086468 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | LYST | GRCh38.p7 | 1:235805666 | GTAATACATATTACA[C/T]TTTTTATATATATAT | 1130 |
rs112127610 | snp | C/G | 0.00156424 | 0.0279226 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810221 | TTTAGCTTTGGGGTG[C/G]TCTTGTTTAGGAAAC | 1130 |
rs112155750 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | LYST | GRCh38.p7 | 1:235680691 | GCAACCTCCACCTCC[A/T]GGGTTCAAGTGATTC | 1130 |
rs112177437 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235783795 | TAAGCTGTTAATAAC[A/G]ACTAATAGAAAGTAT | 1130 |
rs112204158 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | LYST | GRCh38.p7 | 1:235870952 | GTGGTAGAGGAATAC[A/G]AGACTGCGATTTCAG | 1130 |
rs112218560 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | LYST | GRCh38.p7 | 1:235669885 | ACTTGCAGTCAACAC[C/T]CTCTACCAGTGACAC | 1130 |
rs112226795 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713083 | TTCTTCTCCCAGCCT[G/T]AGTTGCTCTGCTGAG | 1130 |
rs112232674 | snp | C/T | 0.00284024 | 0.0375773 | intron-variant | LYST | GRCh38.p7 | 1:235693309 | GGCAGAGTGAGACTC[C/T]GTCTTAAAAATAAAT | 1130 |
rs112240891 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235677931 | CCTATAAGCTTTTTC[G/T]AATCTTGACATTGTC | 1130 |
rs112259171 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867537 | GCAGTGGTGTATTTT[C/T]CAACCGACTCCTGTT | 1130 |
rs112280259 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235802219 | AAAAAAAAAAAAAAA[A/G]ACTAGCAGTACTGGG | 1130 |
rs112280438 | snp | A/G | 1.65269e-05 | 0.00287457 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809696 | CTTTTGTCTTGGTGC[A/G]AAAGGGTCAGGCTGC | 1130 |
rs112292305 | in-del | -/TATTT | 0.0626037 | 0.165477 | intron-variant | LYST | GRCh38.p7 | 1:235767631 | TAGTCACTGGTATTC[-/TATTT]TATTATTTTTTTAAT | 1130 |
rs112302922 | in-del | -/AA | 0.171704 | 0.237423 | intron-variant | LYST | GRCh38.p7 | 1:235674403 | AGAAAGAACAATCGT[-/AA]AAAAAAAAAAAAAAG | 1130 |
rs112312251 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | LYST | GRCh38.p7 | 1:235849055 | AAAACCAGGAAAGGA[C/T]ATAACCAAAAAGAGA | 1130 |
rs112325775 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235681167 | GGATTCCCTGGAAGA[C/T]GGCATATGAACTGAA | 1130 |
rs112333904 | snp | A/G/T | 0.0325976 | 0.123435 | intron-variant | LYST | GRCh38.p7 | 1:235667808 | GCTGGGACTACAGGC[A/G/T]AGTGCCACCATGTCT | 1130 |
rs112333912 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | LYST | GRCh38.p7 | 1:235778510 | CTCCTGAGTAGCTGG[A/G]ATTACAGGTGCATGC | 1130 |
rs112348446 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | LYST | GRCh38.p7 | 1:235698011 | CTTCAAGCAAAAACA[A/G]TTATTAAAAAGTTTC | 1130 |
rs112363684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235818586 | TGTATAGCTCATACT[C/T]AGTATACCTCAACAT | 1130 |
rs112373166 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | LYST | GRCh38.p7 | 1:235846076 | CAACCAGTACAAAAA[C/T]AGAGCATTAAACCAC | 1130 |
rs112405035 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235721423 | CTGATTGAAAACATA[C/T]ATAAACTCTTTTTTA | 1130 |
rs112414449 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235774669 | ATGGCCCACCCAGGT[C/T]TAAAATTCAATGAGT | 1130 |
rs112419642 | snp | A/G | 1.8249e-05 | 0.00302062 | intron-variant | LYST | GRCh38.p7 | 1:235757267 | AAAATAACATATCTA[A/G]TATTTGCCCTTACTT | 1130 |
rs112426479 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751304 | GTCATGATTTGCGGT[A/G]GTCCTTATAAATTCC | 1130 |
rs112448258 | snp | C/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235784664 | CTACTTTATAGTATT[C/G]TTGGGAGGATTAAAT | 1130 |
rs112450064 | snp | C/T | 0.116488 | 0.211364 | intron-variant | LYST | GRCh38.p7 | 1:235686123 | TATAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 1130 |
rs112460353 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | LYST | GRCh38.p7 | 1:235859236 | ACCTGACTCTTCCAT[C/T]TCCTCTCGTTACATT | 1130 |
rs112471514 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235871923 | TTTCCTCAACCCTCC[A/C]AGGGTTCCTGGCTGG | 1130 |
rs112475265 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235842610 | TGCCGAATGAATGGC[A/G]TGGCCTCTCTCTCAG | 1130 |
rs112475652 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | LYST | GRCh38.p7 | 1:235847365 | CCACCACTAGAAGAA[C/T]TGCTAAAAGGAGCTC | 1130 |
rs112481538 | in-del | -/A | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235690512 | TGATGTTTCAAAACT[-/A]AAAAAAAAAATCTTA | 1130 |
rs112498714 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235668396 | AAAAAATTATGTTCC[C/T]TATATACCAAGTGCT | 1130 |
rs112501464 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738346 | GTGTAATGTGAACAT[A/C]TTTAAATTCATCATT | 1130 |
rs112503406 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867388 | GAAGGAGTCAGGAGA[A/G]GGAGAAAGGGTTACC | 1130 |
rs112513572 | snp | A/G | 0.166832 | 0.235761 | intron-variant | LYST | GRCh38.p7 | 1:235691885 | GCATTTTTCATAGAG[A/G]CAGGGTTTCACCATG | 1130 |
rs112529148 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235697468 | CCTTATTTGAGTTTT[A/T]CTCTGTGGTTCTGGC | 1130 |
rs112546169 | in-del | -/ATA | 0.0626037 | 0.165477 | intron-variant | LYST | GRCh38.p7 | 1:235742880 | ATAGTTAAGTACCGT[-/ATA]ATAAGGTATTTACTC | 1130 |
rs112551530 | in-del | -/ATT | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235720344 | AGATGATATCATGGA[-/ATT]ATTGTCAATTTTCTT | 1130 |
rs112561536 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235807141 | TGGACACCCTGAGGG[A/C]AGGCAAGCACGTGTT | 1130 |
rs112568531 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235691209 | AGGCTTGAGCCACCG[C/T]GCCTGGCTACAGTTT | 1130 |
rs112572157 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | LYST | GRCh38.p7 | 1:235842717 | TTCCCTGGATTATTT[A/C]CTTTACCTTCTGGAA | 1130 |
rs112576518 | in-del | -/C/TC | 0.0901694 | 0.192235 | intron-variant | LYST | GRCh38.p7 | 1:235783887 | AATTCTTTTTTTTTT[-/C/TC]TTTTAAATTGAGACA | 1130 |
rs112601869 | snp | C/T | 0.0040622 | 0.0448843 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759041 | AAGTTTTCCCAATCA[C/T]CAGTGTTTCTATCAA | 1130 |
rs112605533 | snp | C/T | 0.177503 | 0.239258 | intron-variant | LYST | GRCh38.p7 | 1:235680291 | GACAGGGTCTCACTC[C/T]GTCACCCAGGCTGCA | 1130 |
rs112680016 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235848948 | CAGACATTTAAAGAA[C/T]TGGTACCAATCCTTT | 1130 |
rs112703420 | snp | C/T | 0.167484 | 0.23599 | intron-variant | LYST | GRCh38.p7 | 1:235691989 | AGGCGTGAGCCACCA[C/T]GCCCAGCCTAACATC | 1130 |
rs112716304 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235705358 | GTCAGATGAGAATTA[A/C]CATGTGTATTTCAGT | 1130 |
rs112739986 | snp | G/T | 0.000478402 | 0.0154587 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806367 | GCCAGAAGTATCTTC[G/T]GAGTCATTGGCCGAC | 1130 |
rs112755993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677035 | GGAGTAACCACTGGC[C/T]GAATGCGCTGTTAGA | 1130 |
rs112793742 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235783158 | TGTAAGATGAAGACA[A/G]GATAAGCTAACACGG | 1130 |
rs112801435 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235744798 | ACAGCTACTCAGGAG[A/G]CTGAGATGGGAGGAT | 1130 |
rs112803361 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235802438 | TCACAGACAGGTGTC[C/T]GCATTCCTGTATTAT | 1130 |
rs112804460 | snp | C/T | 0.5 | 0 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810056 | ATGACATAAGTCAAA[C/T]GGAGAATTGTTCATG | 1130 |
rs112819655 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235733239 | TTCAGTGATTTCTCT[A/G]TTCTTTTACAGACCA | 1130 |
rs112830771 | snp | C/T | 0.5 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808885 | ATTGGGCTAGTTGGT[C/T]AGAGTCAACAGTACA | 1130 |
rs112831882 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | LYST | GRCh38.p7 | 1:235850601 | AAACAACCCACAGAA[C/T]TGGGAGAAAATCTTC | 1130 |
rs112839638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872209 | GCTGAAGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 1130 |
rs112840886 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235664284 | TAAAACTTCAAAACT[A/G]TGCTAAAGCTATCTT | 1130 |
rs112842013 | snp | C/T | 0.089084 | 0.191327 | intron-variant | LYST | GRCh38.p7 | 1:235805681 | TTTTTTATATATATA[C/T]GTGTGTGTGTATATA | 1130 |
rs112843904 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | LYST | GRCh38.p7 | 1:235864609 | CAAAGTCTATTCTCC[A/G]TCCAGCGCCCAGAAT | 1130 |
rs112860628 | snp | A/G | 0.174288 | 0.23826 | intron-variant | LYST | GRCh38.p7 | 1:235691879 | ATTTTTGCATTTTTC[A/G]TAGAGGCAGGGTTTC | 1130 |
rs112879372 | snp | A/T | 0.0832709 | 0.186283 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738092 | TGGGGTTGGTGCTCT[A/T]GGCATGGCCTGTGCC | 1130 |
rs112884652 | in-del | -/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235680602 | ACACAAGTGATTTTC[-/T]TTTTTTTTTTTTTGA | 1130 |
rs112888913 | snp | C/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235791548 | GACAACTCATGCTTT[C/G]ATAAGTCAGGACCTA | 1130 |
rs112897593 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235758284 | CTTAAGTTTCTGGAG[A/G]GAGAACAAACTGGGG | 1130 |
rs112938240 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235818342 | AACTTTCCCAAACAT[A/G]CTTCTCAGTCTTCTC | 1130 |
rs112954198 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235677355 | GTAATCTTACTACCT[C/T]TAAGCATGTGTTTCA | 1130 |
rs112961250 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235697431 | TTTACTTCCCCATGC[G/T]TAGCGTATAGAAATA | 1130 |
rs112986849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235769834 | TTTATTTAAGGAATA[C/T]GGAACAAGTTAAAAT | 1130 |
rs112987289 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235821402 | AGATTGTGCCAATGC[C/T]CTCCAGCCTGCATGA | 1130 |
rs112997604 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846415 | GACAGAGCCTACCCA[A/T]ATGAGAAGGAACCAG | 1130 |
rs113006318 | in-del | -/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235765842 | CTTACCAAATACACA[-/T]TTTTTTTTTTTACTG | 1130 |
rs113012035 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235813254 | AAGCCTTTCTAATGA[G/T]AGAAGAATCTAAGAG | 1130 |
rs113014483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835305 | ATCAAACTGTAAGCC[G/T]AAAGATGGTATTATA | 1130 |
rs113016728 | in-del | -/TACT | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235815436 | GGCTATTTGAGCAGA[-/TACT]TAATTGATGAGAAGA | 1130 |
rs113018128 | snp | A/C | 0.0670745 | 0.170406 | intron-variant | LYST | GRCh38.p7 | 1:235778212 | GTGCCTCCCAGAGTG[A/C]TGGGATTATAGGCAT | 1130 |
rs113026979 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235875955 | CCGGGCATAGTGACT[C/T]GTGCTTGTAATCCCA | 1130 |
rs113047972 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235697557 | AAAAAAATTTAGTAC[A/C]TTTCTTATTTCTAGT | 1130 |
rs113059697 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235798515 | CCTGGGAGGTGGAGG[G/T]TGCAGTGAGCTGAGA | 1130 |
rs113066099 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235692311 | GTACTCCAGCCTGGG[C/T]GATGGAGCGAGACTT | 1130 |
rs113076324 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235741818 | GGCATACAACATTCA[A/T]AGCAGCATCACTCAA | 1130 |
rs113094802 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235699403 | TCATCCATGTCCCTG[A/C]AAATGACATGATCTC | 1130 |
rs113098490 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235807568 | TAACATCAATAATAG[C/T]TTTAAAGTAGTTGTG | 1130 |
rs113145164 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235695117 | TAAACACTGACCTCT[-/C]CCAGACCCTAGGGTA | 1130 |
rs113149431 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | LYST | GRCh38.p7 | 1:235846146 | CCACCTGCACCAGAA[A/C]AGGCGCTGGTATCCA | 1130 |
rs113179189 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235688309 | CATCACTACTCATCA[A/G]TTATTCCTAAATACG | 1130 |
rs113182046 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235663184 | GTTATCTTCAGTGGC[A/G]CAGAGAGACATAAAC | 1130 |
rs113184829 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235663745 | ATTCCAGAGACACAC[C/T]ACAAGCATGCCTTTC | 1130 |
rs113187379 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | LYST | GRCh38.p7 | 1:235792417 | CCTCCCAGGTTCAGG[C/T]GATTCTCCTGCCTCA | 1130 |
rs113199222 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235848174 | AAAACTGAAATTATA[A/T]CAAGCACTCTCTCAG | 1130 |
rs113209379 | snp | A/C | 0.000446728 | 0.0149387 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744103 | AAAACTGAGGTCTTG[A/C]TTTGAGTTACATTTT | 1130 |
rs113243985 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235683575 | TTCAACAGAAACTTA[C/T]GGTGCTCAAAGTTAG | 1130 |
rs113254742 | in-del | -/T | 0.26078 | 0.249767 | intron-variant | LYST | GRCh38.p7 | 1:235717707 | ACATGTTGATACATC[-/T]TTTTTTTTTTTAATA | 1130 |
rs113260282 | snp | A/C/T | 6.59201e-05 | 0.00574078 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702924 | TATCATGGTTTCTAG[A/C/T]GCTCGTCTCTGAACT | 1130 |
rs113301642 | snp | A/C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | LYST, MIR1537 | GRCh38.p7 | 1:235853001 | GTCTGGCACAACTTA[A/C/T]AACTGTAACTAGACG | 1130 |
rs113336432 | in-del | -/ATTAC | 0.0898077 | 0.191933 | intron-variant | LYST | GRCh38.p7 | 1:235812204 | AGCTTGAAACAAAAT[-/ATTAC]ATTAAATATATCCTT | 1130 |
rs113344215 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235689634 | TGAAATTTGCTAAGA[C/T]AGTAGATCTTAAATA | 1130 |
rs113369337 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | LYST | GRCh38.p7 | 1:235831100 | AAATCCCCAAGGAGT[C/T]TCAAAATAGTTTCAT | 1130 |
rs113373611 | in-del | -/TACTGTGTCCCTGG | 0.0980852 | 0.198549 | intron-variant | LYST | GRCh38.p7 | 1:235702671 | GACCATGCTATTCAT[-/TACTGTGTCCCTGG]CACCTGGGAGAGTGC | 1130 |
rs113374433 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | LYST | GRCh38.p7 | 1:235855526 | AAAGATAATCCAAAG[C/T]ATACAGTTTAAAAGT | 1130 |
rs113389019 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235801966 | TTTGGGAGGCCGAGG[A/C/T]GGGTGGATCACGAAG | 1130 |
rs113407870 | snp | A/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235693847 | AGATACTATTTAACT[A/T]TCTAGATACCCAGGA | 1130 |
rs113415914 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235690887 | AGCATACTGTATATT[C/T]ACATGGTATTTTACA | 1130 |
rs113418101 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744009 | TCCTTCTACCAGATA[C/T]GTAAAAATTTCTTTC | 1130 |
rs113440893 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235669679 | CCAATGGGAAACCTC[C/T]GCAGGGTATTTGTAC | 1130 |
rs113454549 | snp | A/T | 0.0633504 | 0.166319 | intron-variant | LYST | GRCh38.p7 | 1:235811873 | TTGTGAATTCTGCAA[A/T]CTCAGAAAAAAATAA | 1130 |
rs113472954 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235771965 | TGGGGGGCTCACGCC[C/T]GTATCCCAGCACTTT | 1130 |
rs113496937 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235720171 | AGAGTGAGACTCTGT[C/T]TCAAAAAAAAAAAAA | 1130 |
rs113505693 | snp | A/G | 0.116138 | 0.211142 | intron-variant | LYST | GRCh38.p7 | 1:235692442 | CTGGAATGCAATGGC[A/G]TGATCTTGGCTCACT | 1130 |
rs113521633 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235795696 | GGAAAGAGGCCAAAA[C/T]AGAAAACAAATTCAC | 1130 |
rs113522995 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235861583 | TTGAAAATCCATTTT[A/T]AAAAATTAGCTTATT | 1130 |
rs113523686 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | LYST | GRCh38.p7 | 1:235837213 | GAGGGTAAGTATCCA[A/G]CACAGGAGACTGAGA | 1130 |
rs113541841 | snp | G/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235787015 | AACAAACCTGCACAT[G/T]GTGCACATGTACCCT | 1130 |
rs113546080 | snp | A/T | 0.122758 | 0.215196 | intron-variant | LYST | GRCh38.p7 | 1:235816445 | ACTCCGTCAAAAAAA[A/T]AAATAAATAAATAAA | 1130 |
rs113560310 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665477 | ATTAGCCAGGGGTGG[A/T]GGCGGGCGCCTGTAG | 1130 |
rs113560541 | in-del | -/C | 0.0509478 | 0.151255 | intron-variant | LYST | GRCh38.p7 | 1:235801415 | ATTCAAACTTTCTGA[-/C]CCCCCCCCTCAAATA | 1130 |
rs113567183 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235752477 | CTAGAGATTAATACA[C/T]GATACTATAAGAACA | 1130 |
rs113591246 | in-del | -/TAAT | 0.115788 | 0.21092 | intron-variant | LYST | GRCh38.p7 | 1:235678130 | CCTTTGGGAAATAAA[-/TAAT]TAAAGTTTTTTAAGA | 1130 |
rs113617516 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235727339 | ATGTTGGCCAGGCTG[C/G]TCTCAAACTCCTGAC | 1130 |
rs113622075 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | LYST | GRCh38.p7 | 1:235779966 | AGTTTTCTAGTTGCT[A/G]TAACGAAAAATCCTC | 1130 |
rs113640913 | in-del | -/A | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235761764 | CTTTGGAGTGTGATT[-/A]AAAAAAAAAACAAAA | 1130 |
rs113655862 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235711935 | ACTTAATAAAAAACA[C/T]TTTCTCTTATTTGGG | 1130 |
rs113683293 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235731252 | AAAAATCATTATAGA[A/G]ATTGAGTAAGTAAGT | 1130 |
rs113694121 | snp | C/T | 0.084728 | 0.187577 | intron-variant | LYST | GRCh38.p7 | 1:235798575 | AAGGGCAAAACCCTG[C/T]CATAAAAAAAAAAAA | 1130 |
rs113699500 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808331 | CTGCTGCCAAAGCCC[G/T]GGAGATATCAGTGTT | 1130 |
rs113703365 | snp | C/T | 0.167809 | 0.236103 | intron-variant | LYST | GRCh38.p7 | 1:235691987 | ACAGGCGTGAGCCAC[C/T]ATGCCCAGCCTAACA | 1130 |
rs113710275 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235727978 | GAGTGACAAAGAATG[A/C/G]ACTCTAATAGTTCTT | 1130 |
rs113721546 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738479 | AAACCATGTTATTGG[A/T]AGTGGTTGCAATCTG | 1130 |
rs113740454 | snp | C/T | 0.105214 | 0.203807 | intron-variant | LYST | GRCh38.p7 | 1:235695757 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 1130 |
rs113766469 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | LYST | GRCh38.p7 | 1:235858419 | TTATAATTAGCACTA[C/T]TAATCTTGGCTATCC | 1130 |
rs113780947 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235763489 | ACAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTA | 1130 |
rs113781347 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | LYST | GRCh38.p7 | 1:235686291 | AGAATTGATTGAGCC[C/T]GGGAGGCAGAGGTTG | 1130 |
rs113786293 | in-del | -/ATATTGGTACACCC | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235881510 | CAGGATCTCAAAGAG[-/ATATTGGTACACCC]ATGTTCATAGCAGCA | 1130 |
rs113787891 | snp | C/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701496 | AGCTGGGTGTGGTGG[C/G/T]GGGCGCCTGTAATCC | 1130 |
rs113799576 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235701136 | GGATATATCTGGGGA[A/G]TGGTTATTCCAGGTG | 1130 |
rs113819775 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235882073 | ACACACACACACTCT[C/T]TCTTTCACACACACA | 1130 |
rs113868421 | snp | A/G | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235708312 | TAACAAAGTACAAGT[A/G]CTTTTTCTGTAATAA | 1130 |
rs113901985 | snp | A/C | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235843851 | AAACAGTAACACCCA[A/C]AAGACTTGTTAGTCT | 1130 |
rs113931667 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868857 | TGTGCTACCATGCCC[A/G]GCTAATTTTGTATTT | 1130 |
rs113938552 | snp | A/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235789676 | CGATGTTAAAAAAAT[A/T]CTCCCTGTAGCGATG | 1130 |
rs113943265 | in-del | -/A | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235869471 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAATAAT | 1130 |
rs113955144 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235681168 | GATTCCCTGGAAGAC[A/G]GCATATGAACTGAAG | 1130 |
rs113957818 | snp | C/T | 0.5 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235751543 | TTTAAAGCAAATTTA[C/T]AAATGGTCACTAAAA | 1130 |
rs113988478 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235799294 | TCATAATACTAAAAT[C/T]AGTGGATGAAAGAAT | 1130 |
rs114037306 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | LYST | GRCh38.p7 | 1:235717812 | TCATAAAAACCTTGT[A/T]AAAAAGCAAAAACAA | 1130 |
rs114079442 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | LYST | GRCh38.p7 | 1:235795430 | CTGTATGCCAAGCCA[C/T]GCATCCTGGTTTTGG | 1130 |
rs114109609 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235841465 | ACTGGCACCATGTTG[A/G]TAGCTTAAAATCATC | 1130 |
rs114113623 | snp | C/T | 0.0448719 | 0.142907 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854646 | TAGCTGTAGTTGTTG[C/T]GAATATCAACATTAA | 1130 |
rs114120967 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235700403 | AAAAACAAACGACCT[C/T]ATGAAAAAGTGGGCA | 1130 |
rs114165158 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235735937 | TAAAAACGGTACATG[A/G]CTAAAAGACTTTCCT | 1130 |
rs114177384 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235876841 | GCCTAAGCTATGTTT[A/C]TGACTAGAATTTAGA | 1130 |
rs114205329 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235799567 | ATGAGAAAACATCAT[A/G]CAAACCAAAATTAAA | 1130 |
rs114205478 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235749139 | AGTATCATGGACAAA[C/T]GGACTTGAATTAGTT | 1130 |
rs114228389 | snp | C/T | 0.0444908 | 0.142359 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826421 | ATTACAGTACACCCA[C/T]ACAATGAAATACTAA | 1130 |
rs114243377 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235683285 | ATTGTTCTTGAATGA[A/G]GTAATACTACCTTGT | 1130 |
rs114262417 | snp | A/C/G/T | 0.0186161 | 0.0948403 | intron-variant | LYST | GRCh38.p7 | 1:235821207 | CTTTGGGAGGCCAAG[A/C/G/T]GGGGTGGTTGCTTGA | 1130 |
rs114308678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706091 | AGCCACCATGCCTGG[C/G]CTCCTAATTGCTTTT | 1130 |
rs114351065 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235849088 | ACTACAGAACGATAT[A/C]CTTGATGAACACAGA | 1130 |
rs114406940 | snp | C/T | 0.040671 | 0.13668 | intron-variant | LYST | GRCh38.p7 | 1:235702592 | ACACAGCATTTACCT[C/T]GCACAGGATTCTGCT | 1130 |
rs114419612 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235851838 | AAGATATGACACTTA[A/C]AGTTCTAAATTAAAT | 1130 |
rs114422815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235737638 | GTTAAAATGAAAAAG[A/G]CCATGTCGACACAAC | 1130 |
rs114462328 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235686049 | GACACATATCCTCAA[C/T]TGCACCACAGGCAGT | 1130 |
rs114464102 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | LYST | GRCh38.p7 | 1:235677981 | ATGTTATAATATTCT[A/C]TACAGTTAGTACCCC | 1130 |
rs114490074 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235836334 | ATAGTGAGGTGGAGA[C/T]AGATGAAAAGCAAAC | 1130 |
rs114499293 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | LYST | GRCh38.p7 | 1:235778385 | TTTATTTATTTATTT[A/T]TTTTTCCGAGACGGA | 1130 |
rs114501043 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | LYST | GRCh38.p7 | 1:235732201 | TGCCCAATAAAGAGG[C/T]AGATGCATTGTAATG | 1130 |
rs114505513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235748354 | ACATTTAAAAGTATA[C/T]ATTGCTACCTTATTT | 1130 |
rs114524618 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | LYST | GRCh38.p7 | 1:235855298 | TTCATTTAATACTAA[C/G]TTTGATAGAAAACAT | 1130 |
rs114582553 | snp | C/T | 0.078151 | 0.181571 | intron-variant | LYST | GRCh38.p7 | 1:235745057 | AATTCCATTTTGACT[C/T]ATCTATAGTGTTTTT | 1130 |
rs114621221 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235860211 | TTAGAAGAGTTTTAG[A/G]TTCACAACAAAACAG | 1130 |
rs114663885 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | LYST | GRCh38.p7 | 1:235718376 | CACTTTTTTTTTTTT[C/T]CAGACAGTTTCACTC | 1130 |
rs114673990 | snp | C/T | 0.00679829 | 0.0579045 | intron-variant | LYST | GRCh38.p7 | 1:235830440 | CTATAAAATAAGTAT[C/T]ACAAAAAAAAAAGAT | 1130 |
rs114711880 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | LYST | GRCh38.p7 | 1:235825055 | CAACAACAACAACAA[A/C]AAAAACGATCAAGAT | 1130 |
rs114737815 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235715410 | GGGCTCCAGGCAACG[A/C]TAGAAAAGTGCTGGA | 1130 |
rs114743028 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235823917 | AAGACAGTCGCTGTC[C/T]TTTCATCTCCGCATC | 1130 |
rs114747436 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | LYST | GRCh38.p7 | 1:235669777 | TTTCATTTTCAATAA[A/G]TTCCTGCTTTTGTTC | 1130 |
rs114751398 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828333 | GAGGTGATGAAAATA[C/T]TCCAAAATTAACTGT | 1130 |
rs114818239 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235823223 | CACCACTGTCGAGTG[G/T]TTAAGATTTCCACTG | 1130 |
rs114845785 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235814203 | GTGGTATTAGGTTGG[C/G]ATAAAGATGATGGAT | 1130 |
rs114877472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235692681 | GAGCCACTGTGCCCA[A/G]CCAGTCTGACTCATT | 1130 |
rs114878970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235817228 | AAGAAAAAAAAAACA[C/T]GCTGGTGAGGTTGTG | 1130 |
rs114944837 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235715679 | TAAGCTGATCAAGCA[C/T]CCAACAAATGAGAGG | 1130 |
rs114963269 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235819561 | ATATTAGACAATATA[C/T]GCCATGAACAGGTCC | 1130 |
rs114965205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235796501 | AATCCAAAGAAAATA[C/T]GCAAATAGCTAAAAA | 1130 |
rs114985620 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235843563 | GCTCAGTACTAGCTG[C/T]ACACCTTATGACAGA | 1130 |
rs115006985 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | LYST | GRCh38.p7 | 1:235881257 | GTTTCAACAGGTTTG[C/T]AAGTTCTTCTGTGTG | 1130 |
rs115007448 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235715556 | GTGCCTCACTAAGAC[C/T]CAAACACTCAGAAGC | 1130 |
rs115009332 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | LYST | GRCh38.p7 | 1:235773248 | CATCTGAGCCTGGGG[A/G]TGGAGGTTGCAGTGA | 1130 |
rs115019462 | snp | A/G | 6.59544e-05 | 0.0057422 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809337 | TTTCTTGTACACATC[A/G]AATGATGAAGTTGCT | 1130 |
rs115051661 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854488 | GGTGAGAAACCAGAA[A/T]AGCACTTCATCTAGT | 1130 |
rs115053004 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235830619 | AATTCCTTCCATGGC[A/G/T]AAATGAGTCCCAGGC | 1130 |
rs115119518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818309 | AGGAGTTCAGGTTTA[C/T]CTCTAAATATGATGG | 1130 |
rs115170447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735680 | ATTTTAAACTGTGAA[A/T]AGTATTAAATGTCAG | 1130 |
rs115174118 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235783679 | AATAAAAATAAAATA[A/G]TGTTTTTAAGGGTGA | 1130 |
rs115181034 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235761687 | ATACTTTCCAACTGA[A/G]TAACTGCTGAAGTTA | 1130 |
rs115181453 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235814895 | ACACATGAGCCCTCC[A/G]CATACATCTAGCTGG | 1130 |
rs115181951 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | LYST | GRCh38.p7 | 1:235674635 | GGGATGCCATTAAAG[A/G]AATAGCTGAACAATT | 1130 |
rs115189647 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235787539 | TTTATACCATAAGTT[A/G]CTTAGTTATTCTATC | 1130 |
rs115194030 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235761189 | AGTGCTAGAGAATAA[A/C]TGAAACACTTTGGCA | 1130 |
rs115216800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821785 | TCAATGGCAACAGGA[C/T]TGGCCTGTAGGCCGT | 1130 |
rs115230933 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | LYST | GRCh38.p7 | 1:235844252 | ACATCAGTAAAAATA[A/C]AAAATCTTTATGAGA | 1130 |
rs115255552 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235824124 | GAATAAAGTACTCTC[C/T]TACATAGAAAATAGC | 1130 |
rs115258124 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235752792 | TCTGGGTTTTCCAAA[C/T]CAAGAAAGGGTTAGA | 1130 |
rs115274599 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | LYST | GRCh38.p7 | 1:235877205 | AAAGAGAATGGCTGG[C/T]CCTGTCCCGCTATCA | 1130 |
rs115307118 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235836722 | AGAATGCAAGTCCCT[C/T]CCAATGCCCACCCAA | 1130 |
rs115322330 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235767797 | TCTTGCCTTATCCAT[A/G]CTATTGAAATCTTGT | 1130 |
rs115327756 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235690846 | GAAGGCTGTCCATAC[A/G]ATTTACAGTCTGGAA | 1130 |
rs115330112 | snp | A/C | 0.00922691 | 0.0672928 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775029 | TGTATTTAATTAATG[A/C]GAGTATAACTCGCAG | 1130 |
rs115414972 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | LYST | GRCh38.p7 | 1:235669052 | AACAAAACCCTAACA[A/G]GTATCTGTGGTATAA | 1130 |
rs115418888 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739673 | GAAAGTTCTTCCCTA[C/T]AGTAAAGTCAGAGCT | 1130 |
rs115422909 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | LYST | GRCh38.p7 | 1:235684863 | CAAATTTCTGGGCTC[A/G]AGCGATCTTCTTGTC | 1130 |
rs115430903 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | LYST | GRCh38.p7 | 1:235691840 | TAGCTGGGATTTACA[A/G]GTGCCCACCACCATG | 1130 |
rs115441306 | snp | A/C/T | 3.29659e-05 | 0.00405981 | intron-variant | LYST | GRCh38.p7 | 1:235693513 | GGAGAAAGAAAAGTA[A/C/T]CAGATTGTCACTGCT | 1130 |
rs115454244 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235838046 | TGGCAGTTCATCTAA[C/T]TGAATAAGAAGAATG | 1130 |
rs115463062 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | LYST | GRCh38.p7 | 1:235862363 | GTCTGAAAATATTAA[A/G]TGGAAAATTCCAGAA | 1130 |
rs115464470 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | LYST | GRCh38.p7 | 1:235667665 | GCACATCCTCCTGTA[C/T]TCTTTTTTTTTTTTC | 1130 |
rs115476750 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | LYST | GRCh38.p7 | 1:235698009 | CACTTCAAGCAAAAA[C/G]AGTTATTAAAAAGTT | 1130 |
rs115493478 | snp | C/G | 0.031825 | 0.122064 | intron-variant | LYST | GRCh38.p7 | 1:235761631 | GGTTAGCATTTTTCA[C/G]TTCAAGAATACCAAT | 1130 |
rs115527309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768759 | TGAACTTAATGAAAA[C/T]TGGCCAATATATTTC | 1130 |
rs115543854 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235674270 | TTTTCATCCCCAAGC[A/C/G]GATGTATGGTAGTAT | 1130 |
rs115581194 | snp | C/T | 0.00147532 | 0.0271198 | intron-variant | LYST | GRCh38.p7 | 1:235781913 | GTGCAGTGGTGCAAT[C/T]ATAGCTCACTCACCG | 1130 |
rs115604887 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235671918 | CCAGTTAGGTTATTA[C/T]AGTGTTCTAGGTAAC | 1130 |
rs115608128 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235795351 | GAGTGTAACTGTACA[A/G]TCTGCAGACTGAACA | 1130 |
rs115654884 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | LYST | GRCh38.p7 | 1:235857426 | GTTGGGATTTGAAGA[A/G]AGTTCTAGATTCATC | 1130 |
rs115656192 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235815939 | AGATCGAGACCATCC[C/T]GGCCAACTGGTGAAA | 1130 |
rs115758460 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235743222 | TGCTGATCAAATCAC[C/T]TGTATCTGGTTCAAA | 1130 |
rs115789221 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | LYST | GRCh38.p7 | 1:235761445 | GTAGCGATGAGACTC[C/T]GTTAAGAGTCAATTA | 1130 |
rs115795471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864530 | ATTATCTCTGGCCTG[C/G]ATTAGGGCAACAGTT | 1130 |
rs115799795 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | LYST | GRCh38.p7 | 1:235859244 | CTTCCATTTCCTCTC[A/G]TTACATTTGATCAAT | 1130 |
rs115804344 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | LYST | GRCh38.p7 | 1:235848197 | TCTCTCAGACCACAG[C/T]GGCATAAAACTGGAA | 1130 |
rs115818700 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235819131 | GCTGGAATTGTAGTC[C/T]TGAAGAGGGCATCCC | 1130 |
rs115822308 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | LYST | GRCh38.p7 | 1:235835851 | ACAAGTTACTTAAGG[C/T]CAGGGACCCTGTCTT | 1130 |
rs115841482 | snp | C/G | 0.129664 | 0.219133 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827335 | GATTGTGCCGCTGCA[C/G]TCCAGCCTGGGTGAA | 1130 |
rs115860826 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235857464 | GAACATTCAGAAGTC[A/G]TTAACATATAGGTGG | 1130 |
rs115868536 | snp | A/G | 0.0387552 | 0.1337 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883640 | CTTAGAAGCCCTTGC[A/G]TTGCTTTTTCGTTTG | 1130 |
rs115893654 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235718489 | TTGGTCTCGAACTCC[C/T]GACGTCAGGTGATCT | 1130 |
rs115968700 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | LYST | GRCh38.p7 | 1:235755927 | AGACTGGCAGCCTTA[A/G]TTGAGTATAAATAGA | 1130 |
rs116007355 | snp | G/T | 0.0372196 | 0.131242 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868341 | ATGCGCTAAGTATTG[G/T]GCTAGGTGCATGGGC | 1130 |
rs116015648 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | LYST | GRCh38.p7 | 1:235678604 | TAGAAAGAATAAGTA[C/T]AATAAAGAGCTATAT | 1130 |
rs116017878 | snp | C/T | 0.000314322 | 0.0125325 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741521 | TGCAGCGTGGGCTGG[C/T]GACAAAATATGCACT | 1130 |
rs116104377 | snp | C/G/T | 0.00769453 | 0.061548 | intron-variant | LYST | GRCh38.p7 | 1:235677043 | CACTGGCCGAATGCG[C/G/T]TGTTAGAGCACCAGC | 1130 |
rs116107364 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235687314 | TACGTGCCTGTGTGT[A/G]GATATATGTGTATAT | 1130 |
rs116120617 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, missense | LYST | GRCh38.p7 | 1:235740572 | TTTCTGAGATTCATC[C/T]ATAATGGTAGATGTA | 1130 |
rs116144545 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | LYST | GRCh38.p7 | 1:235706788 | GAAGCCTATCTTATT[C/G]TCTTTTCTAGATTAT | 1130 |
rs116151846 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235696058 | AGAATGAACCATTGA[C/T]AACACAATAATTATG | 1130 |
rs116173298 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235872945 | AAGTTGGGAAGAAAA[A/G]GAATAATATTTCCAG | 1130 |
rs116174129 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235863130 | CAGCACGGTGGCTCA[C/T]GCCTGTAATCCAGGC | 1130 |
rs116199647 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235880787 | CAAAGATTTTTCTTA[C/T]GCAAATGGGAAGAAC | 1130 |
rs116211415 | snp | C/T | 0.0162469 | 0.0886536 | intron-variant | LYST | GRCh38.p7 | 1:235664659 | CGGGTTACCAGAATG[C/T]GGCTGTCTCAGAGCC | 1130 |
rs116229025 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | LYST | GRCh38.p7 | 1:235774643 | ATGAAGGGACAGCAT[A/G]GGAGATATCTATGGC | 1130 |
rs116269005 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | LYST | GRCh38.p7 | 1:235870778 | AGAACAGTGCCTGGC[A/G]CTTAGTAGGCACTCA | 1130 |
rs116272222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772679 | AAGCCTTGCCCTATA[C/T]ACCATGGTCCTATCT | 1130 |
rs116284934 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235883722 | TCCCTCTGGCTCTTT[A/G]GCAGGTGGCCACGCT | 1130 |
rs116303374 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235710064 | GCTACATTTTCTAGT[C/T]TGCTGAACACCATAA | 1130 |
rs116350192 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235763970 | GGCTTTCTATGCCTC[C/T]TTACCACCTTGGATA | 1130 |
rs116356882 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235686405 | AAAACAAAACCCCCC[A/C]AAAACAGTAAATTAA | 1130 |
rs116360244 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235735361 | AACTCGCAAACCCCA[C/T]GCAGACAATTCTATG | 1130 |
rs116361028 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235668959 | CAAAAATTCTTTCAT[A/G]TCTGAAATCTAATCA | 1130 |
rs116366203 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235830049 | TATTTCAGACGTTTT[A/G]AAAGTATTCAAATAA | 1130 |
rs116375222 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235844804 | TTGTTCAGATTAATA[A/C/T]AATTCTCTTTAAAGA | 1130 |
rs116378941 | snp | C/T | 0.0494327 | 0.149241 | intron-variant, splice-acceptor-variant | LYST | GRCh38.p7 | 1:235740662 | TATACAGATTTCTCT[C/T]TACAGGTATAAAGAA | 1130 |
rs116397326 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865919 | ACGAACGCATTCAAC[A/C]CAAGATTCGACTCCC | 1130 |
rs116485745 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | LYST | GRCh38.p7 | 1:235769244 | AATGGGATCAATAAT[G/T]GTTAAAGCAAAAAGA | 1130 |
rs116493678 | snp | A/C | 0.046775 | 0.145601 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868302 | CTTATCACTCATTTA[A/C]GCAGTATATAATGAG | 1130 |
rs116495065 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235860243 | GAGGCAATTACAGAG[C/T]TTCCATGTACACCCT | 1130 |
rs116541593 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | LYST | GRCh38.p7 | 1:235732709 | TAGCCTCTAGCAATA[C/T]TGAATATTTTCCCGT | 1130 |
rs116551057 | snp | A/G/T | 0.000663459 | 0.0182018 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788841 | ACCTTCTGGTCTGTC[A/G/T]CTCTCTATAAGAAAA | 1130 |
rs116553564 | snp | A/G | 0.029116 | 0.117091 | intron-variant | LYST | GRCh38.p7 | 1:235693034 | ATTAAAAAAAAAGTT[A/G]GCCAGGTGTGGTGGC | 1130 |
rs116574620 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235684530 | AGATGTTATAAAATT[A/G]ACATTCATTTTAAGC | 1130 |
rs116611624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235714020 | TGGATGGAGGGAGGT[A/G]ATAGTTCTGTTAAAC | 1130 |
rs116613302 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737793 | TACAAGAATTAGAGG[C/T]TACTAGGGGCATGAA | 1130 |
rs116631603 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | LYST | GRCh38.p7 | 1:235681904 | TAATCTGCTGCTTGA[C/T]TAGCTGTTCCAATGA | 1130 |
rs116635603 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235794959 | CAGAATTATAAGAAG[A/G]AAGAAATCCGTAACA | 1130 |
rs116661564 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853869 | GTAGTTCATTTTTCC[C/T]AAAAACAAACAAATT | 1130 |
rs116664117 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | LYST | GRCh38.p7 | 1:235670662 | CAAGGTAAGAAAAGC[C/T]GCAGGGGCAGTGAAG | 1130 |
rs116669071 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235807333 | ACAAATATTATAAAA[C/G]TTTTTCAGCTCTGTC | 1130 |
rs116678985 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | LYST | GRCh38.p7 | 1:235831235 | CGCTTCAGGGGGAAG[C/T]CCTCCCCACAGTCCC | 1130 |
rs116686392 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235796315 | CAAAGTAAACCATCA[A/C]GAAAGTTAAGAAACA | 1130 |
rs116694525 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235881378 | TGTATATAGCTACAT[C/T]ACCACATTGAAGATG | 1130 |
rs116741122 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | LYST | GRCh38.p7 | 1:235767291 | ACTCTTGGGTATTAC[G/T]GAATTGGAGTACTTA | 1130 |
rs116762746 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235833133 | AACAACATCAGTTGT[A/G]GTGATGGGGACACTT | 1130 |
rs116777367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732554 | TGTTTTTAGGATGAT[C/T]AATACATATTGTCAA | 1130 |
rs116830281 | snp | A/C | 0.0185938 | 0.0946107 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661441 | AATCTCATCTCTGCA[A/C]CTCCATGGACCTCAG | 1130 |
rs116981004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685920 | CCTATGCTAGAAATA[C/T]AGGTTTCACTCAGTA | 1130 |
rs117039531 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235836935 | GAACTAGTGAATCAA[C/T]TTGGGAATCATCAGG | 1130 |
rs117277203 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853607 | TTCATATTTCAGGGT[A/G]TCAATAAACAACATT | 1130 |
rs117307343 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235718876 | TTCACTGTGTTTCCT[C/T]GGCCTTTTAAAAAGT | 1130 |
rs117457528 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235696703 | TTTCAAGGCTATCTC[A/G]ACATCCTTGTTGTGT | 1130 |
rs117462511 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | LYST | GRCh38.p7 | 1:235792965 | CATGGCGCCCTGCCT[C/T]AGATGTTCTCTGGAA | 1130 |
rs117609949 | snp | A/T | 0.000430207 | 0.0146601 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788811 | GAGTCTTTCACCAGG[A/T]TTTATGTACTCTGCA | 1130 |
rs117706462 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235812334 | CATGGTGAAATCCCA[A/T]CTGTATGTACTAAAA | 1130 |
rs117712221 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | LYST | GRCh38.p7 | 1:235873127 | GCAGTTTGTTCAAAG[C/T]ACTCAGCATGCCAAG | 1130 |
rs117763382 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | LYST | GRCh38.p7 | 1:235824627 | TAAAAAGAATGTTTT[C/T]GATATTTAAAAAGAG | 1130 |
rs117773101 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235845944 | TTTAATCTTGGGAGT[C/T]CTAGGGCCCTGCCCA | 1130 |
rs117792524 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | LYST | GRCh38.p7 | 1:235666556 | AAATGGCTGGAATGG[C/T]AAATTTTATTTAAAT | 1130 |
rs118085571 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235815246 | GTACTTCAAATGCTG[C/T]AGTGAACACAATATC | 1130 |
rs137881662 | in-del | -/G | 0.0498117 | 0.149749 | intron-variant | LYST | GRCh38.p7 | 1:235784606 | GGGAAAGTCACTCTA[-/G]GGTCTCAGTTGCCTC | 1130 |
rs137893361 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235691126 | GGTTTCACTGTGTTA[G/T]CCAGGATGGTCTCGA | 1130 |
rs137893490 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235741921 | TACAATGGAATATTA[C/T]TCATCCTTAAAGAGG | 1130 |
rs137895088 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235721542 | CAAGACGAGCTTTGC[A/T]AAAAACAGATATGAA | 1130 |
rs137903712 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235824534 | TCATCTAGTTGATAC[A/G]GGTGCCAAGATTAAA | 1130 |
rs137914440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874312 | TTCTGTATACTTGCA[A/G]TGTTCAAGGCTTTGG | 1130 |
rs137998304 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235848296 | GCATTGGGTCAAAAA[C/T]GAAATCAAGATAGAA | 1130 |
rs138011756 | snp | C/T | 0.000181406 | 0.00952208 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809142 | GCCTGCTGTAGTAAG[C/T]GCAAGCACTGATGGG | 1130 |
rs138014439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235716051 | TTTCCACAGCAATGA[C/T]GCATTTTCAACTGCT | 1130 |
rs138030685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818786 | GCTACGGACACGCTG[C/T]ACTGATAATTCAGCC | 1130 |
rs138037849 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867579 | TGTATACAGTGCGCA[C/G]TGTCAGTGTCATATG | 1130 |
rs138041235 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235682302 | TGTACTCCAGCATGG[G/T]CAAAAGGGCAAGACC | 1130 |
rs138044918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235771167 | AAAGACAAAGCCACA[C/T]GAAAACCAGCAGACA | 1130 |
rs138046829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828251 | GAAAGTAGATTAGTG[A/T]TTGCTTAGGGGTAGG | 1130 |
rs138093488 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853457 | AATGTGTTTAATGAA[A/T]TATTTCCAATTTATG | 1130 |
rs138111566 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | LYST | GRCh38.p7 | 1:235677151 | AGACAGCTGTGACAG[A/G]GCTTTTGTGTCCCGC | 1130 |
rs138129496 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | LYST | GRCh38.p7 | 1:235685860 | TAAAACAAAACAAAA[A/C]AAAAAAAACAAACAA | 1130 |
rs138135210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775311 | TAGTATACAATGACA[A/C]ACAACCTTAGTGGCC | 1130 |
rs138144356 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852703 | AAAACTGCCAGAGTT[C/G]GCATTTAATAAATTA | 1130 |
rs138162439 | in-del | -/T | 0.469148 | 0.120308 | intron-variant | LYST | GRCh38.p7 | 1:235690916 | CAGTTTACAAGTTTC[-/T]TTTTTTTTTTTTTTC | 1130 |
rs138174075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235676479 | GGATCACTCAAGTTG[A/G]GCTGGTATGATAAGG | 1130 |
rs138179493 | snp | G/T | 3.30743e-05 | 0.00406645 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759521 | GTTAGTAGTGAAGAA[G/T]TAGGGAATGCTGGTA | 1130 |
rs138189603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837350 | TGAGAGAAAGCTGGC[A/G]GGTGCAGTGGCTCAA | 1130 |
rs138233117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235674043 | CAAGACCCCACAGCC[C/T]GGGGCAATAAGGCAT | 1130 |
rs138244387 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235703712 | TTAGGTCATCTTCAA[C/T]TCCATTCTCCTCACC | 1130 |
rs138273217 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235788080 | GATAGAATATTTCCA[G/T]AGCATAAGACTTCAG | 1130 |
rs138273484 | in-del | -/AC | | | intron-variant | LYST | GRCh38.p7 | 1:235882069 | CACACACTCACACAT[-/AC]ACACACACACACTCT | 1130 |
rs138289761 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235799215 | GGAAACAGAAAATCA[A/C]TATTTGGCAGATACC | 1130 |
rs138320518 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661729 | ATACATATTTTTATC[C/T]CATGGTAACATATTA | 1130 |
rs138351589 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235700157 | AATCTAGGCAATACC[A/G]TTCAGGACATAGGCA | 1130 |
rs138384085 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828533 | TGTATGTTTATAATA[C/T]TGATTCTTTCAATAC | 1130 |
rs138391419 | snp | A/G | 0.000115742 | 0.00760641 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802973 | TAACCTTCTTCTTCA[A/G]CTAAAAGTTTAAAAC | 1130 |
rs138393416 | snp | A/G | 0.000362973 | 0.0134668 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813058 | CTTCTCTACATGTCA[A/G]TGCCTATGTCAGTAA | 1130 |
rs138413573 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235829088 | GCACACTTGTAGTCC[C/T]GGCTACTTAGGTGGC | 1130 |
rs138421877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235805178 | ATCTCAGGAGAAAAC[C/T]TGTAAGAATGTGAGG | 1130 |
rs138423776 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235744726 | GCAACATGGTGGAAC[C/G]CCATCTCTACAAAAA | 1130 |
rs138425127 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | LYST | GRCh38.p7 | 1:235882812 | AACATCCCACATGAG[C/T]CCATCTGCACACATG | 1130 |
rs138436026 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235664791 | TACACAAGTTGCACA[G/T]ATTTTTCTTTTTCAT | 1130 |
rs138443479 | snp | G/T | 0.00312937 | 0.0394321 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759143 | GTGCTGTGGCTTCGC[G/T]GGAAGGAGGCCAATC | 1130 |
rs138489218 | in-del | -/A | 0.135825 | 0.222405 | intron-variant | LYST | GRCh38.p7 | 1:235847591 | CTAAATGCTCCACTT[-/A]AAAAGATACAGAACC | 1130 |
rs138492734 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235748784 | GTCTAGATGTAATGA[C/T]GGTACTGCTGAAGAA | 1130 |
rs138494204 | snp | C/T | 0.00676944 | 0.0578265 | intron-variant | LYST | GRCh38.p7 | 1:235736219 | CTTATTTTCAGCCCT[C/T]AAAAAACTGATTTAA | 1130 |
rs138496529 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235831671 | ATTACAGTAACTCTC[C/T]TTTAGTATAACAAAC | 1130 |
rs138506576 | snp | G/T | 0.00163573 | 0.0285515 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734650 | AATACAAAACTAACT[G/T]GGCTCCATGCTTTAA | 1130 |
rs138536724 | snp | C/T | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733570 | AATCTACTTTATACA[C/T]TCCTCTAATATGCTG | 1130 |
rs138558633 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773891 | AGTTCCTCTAACAGC[G/T]TAACATCTTGGATTA | 1130 |
rs138559990 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235681614 | ATGAGCTGGGGCAAT[C/G]GTCAGGGGGACATCT | 1130 |
rs138583382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768929 | CAAGAAAGGCAATAA[A/G]ATGTTTTTGTGTTTT | 1130 |
rs138588013 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235823817 | GTTCCTGATGACCCC[A/T]CTCCACTACATTCAC | 1130 |
rs138592380 | in-del | -/A | 0.105214 | 0.203807 | intron-variant | LYST | GRCh38.p7 | 1:235677770 | ACAAAGAAAGAAATT[-/A]AAAAAATTTTTAATT | 1130 |
rs138628105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235841011 | GAAGAACTGAGGCAC[A/G]TGTGCAGAGTCTGCT | 1130 |
rs138651296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235776377 | GGGAGACTATGAAAA[C/T]TTGATAATGTTGCAA | 1130 |
rs138666666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235859040 | TTATTTTCCCCTCAA[A/G]CATACTCCAACCCAT | 1130 |
rs138666760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235807316 | ATTGAACAGTCAATG[A/G]TACAAATATTATAAA | 1130 |
rs138680583 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854079 | TTACACTGACTACTA[C/T]ATCCCTCCTCAAAAG | 1130 |
rs138702663 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235873934 | AAATTACAAGGACTC[A/G]CTAAAACTCATGGTC | 1130 |
rs138712263 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | LYST | GRCh38.p7 | 1:235810914 | TTTGGGAGACTGAGG[C/T]GGGTGGGATCACTTG | 1130 |
rs138773820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709713 | AGCATTTCTAAACTA[C/T]TGGTATTAACATTTT | 1130 |
rs138777800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812123 | TCATGTACTTTATAG[A/G]CATATGATTTCTTCA | 1130 |
rs138787779 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810262 | AATGATGCAGCAGAT[A/G]GGGCCTTCTATGCTT | 1130 |
rs138790361 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | LYST | GRCh38.p7 | 1:235708529 | TGCCTAAACTGTACA[A/T]ACAATGCAGTTTATA | 1130 |
rs138822036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235704603 | CTTTTTAATGAGGTT[A/G]TTTTTTTCTTATACA | 1130 |
rs138824162 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235768399 | CTGTACTCACAAATG[A/T]ATGAAACTGCCTTAC | 1130 |
rs138844168 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235721159 | TAAGAAAAAGTTTGT[A/G]TAGAAAAGTCACTTA | 1130 |
rs138849156 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762762 | ATGGGCTTATTACCA[C/T]AAATCCAGGGCTCAT | 1130 |
rs138853361 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235673560 | CACCGAAGGAGTCAC[C/T]GCCCCCCACAACTGT | 1130 |
rs138922457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235881875 | GATAGAAGGAAATGA[A/G]GAGTTAGTGTTCAAT | 1130 |
rs138936105 | snp | C/T | 0.000510763 | 0.0159725 | missense | LYST | GRCh38.p7 | 1:235697121 | AGAAGACAGAAATTC[C/T]GTGACAAACCACAGA | 1130 |
rs138948537 | in-del | -/ATCCTGTGTTGATTT | | | intron-variant | LYST | GRCh38.p7 | 1:235880414 | TATTCTAAGTCAAGG[-/ATCCTGTGTTGATTT]ATTACTCGGTAAAAG | 1130 |
rs138960509 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235782997 | TGGAAAAGGCAAAAT[A/C]AGGCTTTCTCACAGA | 1130 |
rs138967661 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235832060 | GTTTCTGGGATTTTC[C/T]TTCAAAGCTACTAAC | 1130 |
rs138971303 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235685511 | CAGTGACCATGCAAA[G/T]AAACTTAACAAGAGT | 1130 |
rs138972355 | snp | C/G | 0.000560243 | 0.0167274 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759221 | TCATCTTCTGACCTG[C/G]GTTCTGCTCCCAACT | 1130 |
rs138997532 | snp | C/T | 6.59413e-05 | 0.00574163 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720844 | AGAGCGGTGATGTTA[C/T]CATATTCCAGAAGAT | 1130 |
rs139033643 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235840366 | GAAATTACAGTAAGT[A/T]TGGTATCACAACTAC | 1130 |
rs139034177 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235786817 | AAAAACCAAACACCG[A/C]ATGTTCTCACTCATA | 1130 |
rs139067029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838223 | TGATGAGTGTAACAG[A/G]GTCAAAAAACAGCAG | 1130 |
rs139071059 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802556 | TGCCTCTTCAGAAAG[C/G]ACTTCCCTCACCACC | 1130 |
rs139074609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | LYST | GRCh38.p7 | 1:235808082 | AATTAAACTTGCCCT[A/G]CTCTTGGATATCTGT | 1130 |
rs139110568 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235706039 | CTCAAATGATCCACA[A/C]GCCTCGGCCTCCCAA | 1130 |
rs139159733 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235670051 | CTTGGTCTTTCTTGC[G/T]CTGTACACAGGCCCC | 1130 |
rs139168634 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235698014 | CAAGCAAAAACAGTT[A/G]TTAAAAAGTTTCAAA | 1130 |
rs139179488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845520 | GTGCAAATCCAGCTC[A/G]CAGACTTCACAGGTG | 1130 |
rs139179791 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235793979 | CTGGGACTACAGGCA[C/T]GTGTCACCATGCCCA | 1130 |
rs139179993 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235781841 | TATTTGTTAACTGAG[-/A]AAAAAAACTGGAAAT | 1130 |
rs139180213 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235800474 | AAATTCTATGATAGG[G/T]TATCTACTATATATG | 1130 |
rs139199962 | snp | A/G | 0.000329533 | 0.0128319 | synonymous-codon | LYST | GRCh38.p7 | 1:235662946 | CATTCGCATTCACCC[A/G]GCTGCATAGCTGCTA | 1130 |
rs139217636 | snp | C/T | 4.95103e-05 | 0.00497521 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806449 | AATAGGTTTATTGTG[C/T]TGATATGAACATCTT | 1130 |
rs139238969 | snp | G/T | 9.8894e-05 | 0.00703116 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777198 | AACTTCTTTTGAGCT[G/T]AAGGGTCTTTGAGAG | 1130 |
rs139241715 | in-del | -/TCTG | 0.0577344 | 0.159793 | intron-variant | LYST | GRCh38.p7 | 1:235666016 | AGTAGAGGCTTTGCT[-/TCTG]TCTTTTATTAAGACA | 1130 |
rs139241744 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | LYST | GRCh38.p7 | 1:235778381 | ATTATTTATTTATTT[A/T]TTTATTTTTCCGAGA | 1130 |
rs139266532 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | LYST | GRCh38.p7 | 1:235698817 | GGCAGAGCTTGCAGT[A/G]AGCCGAGATCACGCC | 1130 |
rs139269899 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235798724 | GTTGAAAGCATCATG[C/G]TATGTGAAAGAAACC | 1130 |
rs139296343 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235757147 | TGAGTATTAAGTAAC[A/C]AACTATATTAGTTCA | 1130 |
rs139296428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235699172 | TAGGTATACGTGTGC[C/T]ATGGTGGTTTGCTGC | 1130 |
rs139311415 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750885 | AACTCCTGATGTAGA[C/T]TGCCCTGTTATAATC | 1130 |
rs139357489 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235772204 | CATTTTAGCCTGGGT[A/G]ACAGAGTGTGCTCCT | 1130 |
rs139381516 | in-del | -/A | 0.115438 | 0.210697 | intron-variant | LYST | GRCh38.p7 | 1:235789266 | AATATGGCATGATTT[-/A]AAAAAAAAATATCAT | 1130 |
rs139389248 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235666476 | GGGAGGAGGAATGGG[C/G]AAATAGTGGTGATGG | 1130 |
rs139429081 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712770 | TGAGTAAAATTTCCT[A/G]TGAATGAAAATAAAA | 1130 |
rs139440866 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235701241 | ATACTGCTCAGATAC[A/T]ACTTTAACAGCTAAC | 1130 |
rs139465313 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235820447 | CAATCATGGCTCACT[A/G]CAACCTCCACTGCCC | 1130 |
rs139465347 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | LYST | GRCh38.p7 | 1:235758393 | TGACAGCCTGTCCTG[A/G]GAAACACTGGTATTG | 1130 |
rs139477588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675389 | GACTCCAGCCAATGG[C/T]GAGAGGATACAGCAA | 1130 |
rs139496715 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235757988 | GCAAATATTGGTACA[A/G]GGGAAGAATCTAGCA | 1130 |
rs139500328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871844 | CCGGTGACAGTATCT[A/G]TACTTTACTCAAAAA | 1130 |
rs139508185 | in-del | -/TAATT | 0.0854556 | 0.188216 | intron-variant | LYST | GRCh38.p7 | 1:235811359 | TTCATAGACCTGATA[-/TAATT]TAACTACTTTAAGAT | 1130 |
rs139528098 | in-del | -/G | 0.0498117 | 0.149749 | intron-variant | LYST | GRCh38.p7 | 1:235742767 | AAAGACTTGAATTGT[-/G]CTACATTATTGAGTA | 1130 |
rs139529757 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | LYST | GRCh38.p7 | 1:235674848 | CCGAAAAGTCATAGA[A/C]AAATGGTTTAGAAAA | 1130 |
rs139531322 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766139 | AAGTATTAGTAGGAG[A/G]GTGAACTGCTAAAAG | 1130 |
rs139592393 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235834712 | AATTAGGAAAAAACA[C/T]CCCTTCCTGATGGGT | 1130 |
rs139592929 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235821798 | GATTGGCCTGTAGGC[C/T]GTAGTTTGCTCAGCC | 1130 |
rs139643003 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757401 | CAGGATAAGAAGAAC[C/G]CCACTTAGGAGTTCA | 1130 |
rs139654273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750731 | TATCTGAATGCACTG[C/T]TTCTTCTTTAGCTGC | 1130 |
rs139681086 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235683674 | CCACATCCTATGTGG[C/T]ACTTGGTTGGGGGGC | 1130 |
rs139681138 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235728902 | ATCAAATCACTGGAG[A/G]GCTCATCAGAACATA | 1130 |
rs139687949 | snp | G/T | 1.6574e-05 | 0.00287867 | synonymous-codon | LYST | GRCh38.p7 | 1:235664548 | AGCCACGGAACAGAT[G/T]ATCTCCCTGCAGTGG | 1130 |
rs139691284 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235723028 | AGCAGTGGAAGCAGT[A/C]AGACTCTCGATGTAT | 1130 |
rs139692264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744816 | GAGATGGGAGGATTG[C/T]TTGAGCCCAGGAGGT | 1130 |
rs139694536 | snp | A/C/G | 5.05321e-05 | 0.00502632 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774957 | TTTGTTTGATCAACA[A/C/G]CTGATGAATCATAGA | 1130 |
rs139697440 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235783551 | GGCTTAAAACCTAGA[A/T]GACGGGTTGATGGGT | 1130 |
rs139708462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825422 | TCACAGATGACATCA[G/T]TATTTACATACAAAA | 1130 |
rs139716957 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235877673 | GGCCTCCCAAAGTGC[C/T]AGGATTACAAGCGTG | 1130 |
rs139730124 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739597 | AAAACCCACAATAAA[C/G]CTTGAACAGTGAAAA | 1130 |
rs139738097 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235833829 | CTACTTCAAGAATTC[C/T]TCTTGAGAGGGAATC | 1130 |
rs139772905 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235687676 | CCCCACCCTGAGCAC[C/G]ATGTCCGCAGCAACT | 1130 |
rs139804084 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235843298 | TAATATGCTCCAGCT[C/T]ATTCTATTTTCACTA | 1130 |
rs139840658 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | LYST | GRCh38.p7 | 1:235691759 | TGGAGCGCAATGGCA[C/T]GATCTCAGCTCACTG | 1130 |
rs139850253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235849574 | TAAAGAGGAAGTCAA[A/G]CTTTCACTGTTTGCT | 1130 |
rs139850315 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235796826 | ACAAATCACTCAGTC[G/T]GTGGTATTCCATTAT | 1130 |
rs139859828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820572 | GATGGGGTTTTGCCA[G/T]GTTGCCTAGGCTGGC | 1130 |
rs139863056 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235737644 | ATGAAAAAGGCCATG[A/T]CGACACAACAACTTG | 1130 |
rs139877317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794197 | GGCATTCTTTAAAGA[A/G]ACATAAATCAATATA | 1130 |
rs139882915 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720876 | AGGGAGGTTATTTGT[A/G]AGTATATTGTGGTAT | 1130 |
rs139907712 | in-del | -/AT | 0.312104 | 0.242163 | intron-variant | LYST | GRCh38.p7 | 1:235778098 | AGTTAACCCAGTTAA[-/AT]ATATATATATATATA | 1130 |
rs139917441 | snp | C/T | 6.59467e-05 | 0.00574187 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751229 | AATGCTTTTCCGCTT[C/T]TGAACTACTGCATGA | 1130 |
rs139923692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235801978 | AGGCGGGTGGATCAC[A/G]AAGTCAGGAGTTCGA | 1130 |
rs139924216 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235870723 | ATGGGCTCCACAAGG[A/G]CCACAATCTTTGTTC | 1130 |
rs139934827 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235799857 | TTTCATTGTGTGGAT[C/T]TGAGGAACAAACGAG | 1130 |
rs139987004 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235668881 | ATCTTTTCCCTTTGT[G/T]ATAATCATTAGGAAA | 1130 |
rs140021928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235679187 | CAGATCAGCTTTTAA[C/T]AACAGCAAGAGTAGT | 1130 |
rs140059213 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235772753 | ATTTCCCTCTCCTGG[A/G]CCTGACTCCCCTGAC | 1130 |
rs140096466 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806068 | GAAATTCTGTTTAAA[C/T]CCTGGTTTTCATTTA | 1130 |
rs140100938 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | LYST | GRCh38.p7 | 1:235699999 | GGGAAAGGATTCCCT[A/G]TTTAATAAGTGGTGC | 1130 |
rs140126059 | snp | C/T | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787346 | TAGTAAAACAGCTTT[C/T]ATGTCATCATTTGAA | 1130 |
rs140127039 | snp | A/C/T | 8.24349e-05 | 0.00641965 | synonymous-codon | LYST | GRCh38.p7 | 1:235709112 | ATGAAAAACATTGAT[A/C/T]GCTTGAACAGAAGCC | 1130 |
rs140142068 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235831121 | ATAGTTTCATCTCTG[A/G]GCTAAAAGTAATTTT | 1130 |
rs140142230 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235688679 | GTGAAATCTCAGAGC[A/G]TGAGTCTTTATATAA | 1130 |
rs140159024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235815280 | ATCCTCATGAAGCCT[A/G]CTTCCTAGCACAGGA | 1130 |
rs140229368 | snp | C/T | 8.24396e-05 | 0.00641973 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746397 | TCTCTGCGCAAGTTC[C/T]GTTTCAGTTGCTTGG | 1130 |
rs140255375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735163 | TTGCTAAAGGAATAC[A/C]GGAAAGAAACTGGGA | 1130 |
rs140257372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797687 | TAAGAATAAAACTTA[A/C]GGGGAACATTCCATA | 1130 |
rs140278034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235774426 | TATTTCCACAATGTT[A/G]CCAAATGCTTTCATC | 1130 |
rs140284566 | snp | C/T | 0.000215945 | 0.0103887 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808822 | AAGGACTGGATAAAC[C/T]TGAGGAGAGTTCAGC | 1130 |
rs140290105 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | LYST | GRCh38.p7 | 1:235710375 | TGTGGCTTCAGGAGC[A/G]GCAGCAGCAGGAACT | 1130 |
rs140301542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235695140 | CTAGGGTATTTACAG[A/G]CCAATAAGCATTTAT | 1130 |
rs140302363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771623 | TAGATCTGAAAGTAT[A/G]TATTTATTCAGAGTG | 1130 |
rs140302418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235706515 | GGGGTCTTATTTCCA[C/T]GTGAAGCCTCCCGTG | 1130 |
rs140336386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235862312 | TTTATCCGCAGATTC[A/G]TTTTCCAAGGTTTCA | 1130 |
rs140337815 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235790464 | TCAATGCACATTAGA[C/T]AGCATAATAAATATT | 1130 |
rs140369743 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235715780 | TGCTTCTCTAGAAGT[A/G]GAAATGCAATAGAAA | 1130 |
rs140371239 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | LYST | GRCh38.p7 | 1:235818574 | ATAACATTTCCATGT[A/G]TAGCTCATACTCAGT | 1130 |
rs140402459 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866288 | AGTCAAAGGGTGTCA[A/C]GGACAGGAGGAAAGA | 1130 |
rs140434436 | snp | C/T | 0.00205405 | 0.0319814 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752126 | AACTGCTATGAAAAG[C/T]TGCTGTATATCACAA | 1130 |
rs140438816 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235816034 | ACTCAGGAGGTTGAG[G/T]CAGAAGAATCACTTG | 1130 |
rs140486308 | snp | A/G | 0.000368683 | 0.0135722 | intron-variant | LYST | GRCh38.p7 | 1:235715409 | TGGGCTCCAGGCAAC[A/G]CTAGAAAAGTGCTGG | 1130 |
rs140553419 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235709532 | ATAATTAAATTTGAG[A/C]TCTTTCAACTTTATC | 1130 |
rs140561328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866029 | ATCGGGGATGTTTTG[C/T]TATGTTTTGTTTAAC | 1130 |
rs140577186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235718690 | CATCAGAATATTTTT[G/T]CATATTAAACGAACA | 1130 |
rs140579608 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235844224 | CTCAAAGATCTCATA[C/T]AGTCTTTACAACACA | 1130 |
rs140581294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676077 | GAATTTTCTAACTGT[C/T]CTTTTCTGCTGGATG | 1130 |
rs140648262 | snp | C/T | 8.25021e-05 | 0.00642217 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809252 | CTGGTTTTTAAAAGC[C/T]GAAACCAGAAGACCT | 1130 |
rs140665042 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235679852 | TTTCCATTTCTTCCA[C/G]AGAGGCTGTCCAAGG | 1130 |
rs140670050 | snp | C/T | 3.30071e-05 | 0.00406232 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770170 | AGTACCTGCAAAACC[C/T]GACAAGTCAGTAGAA | 1130 |
rs140698096 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809502 | AAATTAAATCCATGA[C/T]GCTGAATGAATTCTT | 1130 |
rs140701654 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235694213 | AGAGACGGGGTTTCA[A/T]CATGTTGGCCAGGCT | 1130 |
rs140703510 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800901 | AAAAACATTCTTTTC[C/T]TTCTGCCTAATAATT | 1130 |
rs140714283 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235666266 | CACACACACACACAC[A/T]CACAATTTTCTTTAG | 1130 |
rs140715384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692319 | GCCTGGGCGATGGAG[C/T]GAGACTTCATCTCAT | 1130 |
rs140718352 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235747747 | ACTAGGTATTAATAC[C/T]AGAAAACGTGGGAGG | 1130 |
rs140719765 | snp | A/C | 3.36202e-05 | 0.00409988 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752147 | TATATCACAAGCAAG[A/C]AATTTATATTCACTC | 1130 |
rs140748042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235880493 | ACACATCTTTGCCAC[A/G]CCTAATATGTACAGC | 1130 |
rs140780002 | snp | A/G | 3.30918e-05 | 0.00406753 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802945 | TTCAGGATTGCTTTC[A/G]CTATCTGCTTCGTAA | 1130 |
rs140785672 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828288 | GAAGGGATAGGGGAA[C/T]GATAGCTAAAGGGTA | 1130 |
rs140792631 | in-del | -/AGA | 0.0437281 | 0.141251 | intron-variant | LYST | GRCh38.p7 | 1:235671726 | CATAGTGATTAAGAG[-/AGA]AGAATAGTAAGAAGT | 1130 |
rs140798642 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235696162 | ACAACTATAAAACAA[C/T]CATTCATTTCATGAC | 1130 |
rs140821981 | snp | A/G | 0.000149168 | 0.00863493 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809821 | CTACTGACAGAAGAT[A/G]CAACACTGTTCGAAA | 1130 |
rs140833311 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235740716 | TCTGTTGATAAGCAT[G/T]TGAATATTTGTAGTT | 1130 |
rs140846237 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235838856 | TCTCCATGTCAGAGA[A/G]GAGAAGAAAGCTAAG | 1130 |
rs140865907 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235681242 | AAAGGGCACTCTGGG[A/C]TAAGAAGACAGCATG | 1130 |
rs140934482 | snp | C/T | 0.00196261 | 0.0312642 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730874 | CTTGCAGCTTTGTCT[C/T]TGACAGTAGAAGAGA | 1130 |
rs140936012 | in-del | -/ATATA | 0.0372196 | 0.131242 | intron-variant | LYST | GRCh38.p7 | 1:235871528 | TTTAAAGATCATATA[-/ATATA]CTCATTAATTCTTGC | 1130 |
rs140944484 | snp | C/G | 0.000414467 | 0.0143896 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741566 | CTGCATTCGGAAGGT[C/G]TCCTTACAAGACCAC | 1130 |
rs140972230 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235708324 | AGTACTTTTTCTGTA[A/G]TAAGAAAACATGGTG | 1130 |
rs140989272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764300 | TCCTCTTTCCCTCAA[C/T]TAGGCTGTAAACGTC | 1130 |
rs140996664 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235855789 | TAAGCTTTAAATACA[A/C]CTTGCACGTATAGAT | 1130 |
rs141019036 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746351 | CTTGATAAATAATCC[C/T]GTTGACTGCTAAAAC | 1130 |
rs141031757 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661319 | AGATGAGTAGCAACC[C/T]TATTCTAATAGGGGA | 1130 |
rs141041013 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235878428 | ACTCTCCCTGATTCC[-/A]ACCCCCTTGGACACA | 1130 |
rs141045358 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | LYST | GRCh38.p7 | 1:235672173 | TCAAGTTTTGTTTTG[A/G]CTGTGTTAAGTTGAA | 1130 |
rs141065255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235768426 | TTACATCCAATATAC[C/T]ACCAATTTATTAATC | 1130 |
rs141072743 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235858745 | AGTTTTCCATCACAT[C/T]TTCCCTTCCAATCTC | 1130 |
rs141083628 | snp | C/T | 0.000280257 | 0.0118343 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806681 | TCAGAGTTTCAAATG[C/T]TTTTAGAGAATGACT | 1130 |
rs141084661 | snp | G/T | 0.00295889 | 0.0383496 | intron-variant | LYST | GRCh38.p7 | 1:235803092 | GTAATTCAAAGGTTG[G/T]AACATTTGCTTGTTT | 1130 |
rs141143527 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235780368 | ATGATCACACCACTG[C/T]ACCCAAGCCTGGGTG | 1130 |
rs141182103 | snp | C/T | 0.000624253 | 0.0176563 | intron-variant | LYST | GRCh38.p7 | 1:235762879 | TTTTTTTTGAAACAG[C/T]AAAATTTTTAAAAAG | 1130 |
rs141184433 | in-del | -/A | 0.131381 | 0.220067 | intron-variant | LYST | GRCh38.p7 | 1:235832470 | TCTCAACAGAAATGT[-/A]TGTTTTTTCCTGATT | 1130 |
rs141195871 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235880059 | GGATCTAAGTTTCTC[A/G]GAAGAGTGAACTCTT | 1130 |
rs141197189 | snp | A/C | 0.0621959 | 0.165014 | intron-variant | LYST | GRCh38.p7 | 1:235766296 | AAAAAATAAAAAAAA[A/C]TCTCTTTAGATTTAA | 1130 |
rs141199224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854150 | TCTGGCTAACACCTA[C/T]AGTGATTAATTACTA | 1130 |
rs141248903 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235874038 | GACCACTTCAAAGCA[A/G]CAGTTGAAAAGGGTG | 1130 |
rs141259783 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235760967 | AAATAAAACTAATTC[A/G]AAAAGGCCAGGTGCA | 1130 |
rs141260140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822726 | AAGTGATAGAGTCTA[C/T]TTCCCCATCCCTTAA | 1130 |
rs141264552 | in-del | -/T | 0.151001 | 0.229563 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884649 | GTGCTAAAATATGCC[-/T]TTTTTTTTTCCTCCT | 1130 |
rs141309960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235732698 | GAAAACCAAATTAGC[C/T]TCTAGCAATATTGAA | 1130 |
rs141312203 | snp | C/T | 8.42141e-05 | 0.00648845 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830408 | CCAGTGAGTTACTGT[C/T]GGTGCTCATGACCGA | 1130 |
rs141317027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684149 | ATGTATGTCTTGCAG[C/T]ATTTAAATTGTAATA | 1130 |
rs141317482 | snp | A/G | 0.00827251 | 0.0637795 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830422 | TCGGTGCTCATGACC[A/G]AGCTATAAAATAAGT | 1130 |
rs141320974 | snp | C/G/T | 4.94241e-05 | 0.00497092 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720811 | TTAGTAATTTGCCCA[C/G/T]TATACCATAAATTTG | 1130 |
rs141330120 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235685555 | AGCTTGGAAAAAAAA[C/G]TAAGAACCTGGCTGG | 1130 |
rs141336927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235847546 | TGGAACCATACCGCA[C/T]ATTTCAATGCTAAAA | 1130 |
rs141344311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726298 | TCTATGTGTGTTTTA[C/T]TATTGTTCTTGGTCC | 1130 |
rs141381162 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827538 | TGTTATGATTTCATC[C/T]TAAATGATAAAATAT | 1130 |
rs141383979 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235836021 | TCCTTAGCATTTACC[A/G]TAAATGAAAAACATA | 1130 |
rs141394101 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883650 | CTTGCGTTGCTTTTT[A/C]GTTTGGTAACGGGGC | 1130 |
rs141401599 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235689829 | TAGAAAAAAATAAAA[A/G]TAAGAATTTTAAACA | 1130 |
rs141437139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235668398 | AAAATTATGTTCCCT[A/G]TATACCAAGTGCTCT | 1130 |
rs141439277 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235749643 | TCTGTAAGTCTCCTA[C/T]AGCTTGCAGCAATCA | 1130 |
rs141459226 | snp | A/T | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775048 | TATAACTCGCAGTGC[A/T]AATGCTTGAGTTTCT | 1130 |
rs141509909 | snp | C/T | 0.000131804 | 0.00811695 | missense | LYST | GRCh38.p7 | 1:235693421 | TCAACCTTAAAATAT[C/T]ATCAGCATATCCCCA | 1130 |
rs141513956 | snp | A/C | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793584 | ACTCATCAAAGATAC[A/C]AAAAGATCCACCAAT | 1130 |
rs141534829 | snp | A/G | 0.000413637 | 0.0143752 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741512 | TCTCTCTTGTGCAGC[A/G]TGGGCTGGCGACAAA | 1130 |
rs141536165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837116 | ACTATAATGAACAGC[A/G]AGGACCTAGAGAATG | 1130 |
rs141544931 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235744507 | AGAGCTGTTTCTCTG[C/T]ATGTGCTATACATTT | 1130 |
rs141547797 | in-del | -/C | 0.462144 | 0.132269 | intron-variant | LYST | GRCh38.p7 | 1:235783888 | ATTCTTTTTTTTTTT[-/C]TTTTAAATTGAGACA | 1130 |
rs141604693 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235851147 | CAATCAACAAGTGAA[C/T]AAAGAAACTGTGGTA | 1130 |
rs141656220 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235710148 | TTGCTGTCTGTCTAC[C/T]TTTTGATCTTGTAAA | 1130 |
rs141666643 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845524 | AAATCCAGCTCGCAG[A/G]CTTCACAGGTGGAAG | 1130 |
rs141695062 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235860642 | ATGCACTAAAGATTT[C/T]TTCATGTCTTTTCAT | 1130 |
rs141732234 | snp | A/G | 3.3211e-05 | 0.00407485 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809782 | TCCTAAGATTTTCTG[A/G]CATCATCTCTGCAGT | 1130 |
rs141737652 | in-del | -/A | 0.031825 | 0.122064 | intron-variant | LYST | GRCh38.p7 | 1:235705151 | CAAGATATTTGCCCT[-/A]AGGTCACACAACAAG | 1130 |
rs141745214 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235667346 | TATTTTGATCCAGTG[A/G]TAGAATGGTAAACAC | 1130 |
rs141754386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674718 | TTGGCCAAAAAGGGC[A/G]GGGTCTGTGTCATGA | 1130 |
rs141758032 | snp | A/G | 4.94458e-05 | 0.00497197 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806227 | GAACTCAACATGTAG[A/G]TCCAACGACACATAG | 1130 |
rs141764245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235703605 | ATGGCTTAGCTTTTC[A/G]TATATTTAATCAGTC | 1130 |
rs141764855 | snp | A/G | 0.000297049 | 0.0121834 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806693 | ATGCTTTTAGAGAAT[A/G]ACTTCGAATACCATT | 1130 |
rs141799480 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235804392 | CTGAACTCATCTGAC[C/G]AAGTCCTAGTCCATA | 1130 |
rs141804729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235756332 | TCCATGAATCCTTCC[A/G]TTTCCCCTATGCTCA | 1130 |
rs141823118 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235674336 | GTGGAGTGGCATTTG[C/T]GCTCTAATCCAATTA | 1130 |
rs141827492 | snp | G/T | 0.000267363 | 0.011559 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746511 | TTCAGTTTGAGCAAG[G/T]GGAAATTTTCGAGGA | 1130 |
rs141827803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235664870 | GGTGTGATCTTGGCT[C/T]ACTGTAACTGCCTCC | 1130 |
rs141857854 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235832946 | ATAGGAAGTGGATTT[A/C]TTTTGATATAATAAT | 1130 |
rs141862163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700997 | ATGACGGAACAGCTG[C/T]TTTAGACATAATTAG | 1130 |
rs141868568 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235812417 | GAGGCTGAGGCACAA[G/T]AATTGCTTGAACTCG | 1130 |
rs141870442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750845 | CACAACATGATTGCT[C/G]GACACCTTTCTCAGA | 1130 |
rs141905339 | in-del | -/A | 0.0836354 | 0.186609 | intron-variant | LYST | GRCh38.p7 | 1:235747535 | AGTCACTTTTGAGGC[-/A]AAAAAAAAAGAAAAT | 1130 |
rs141911495 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762445 | TAGACAGAAGAGAAT[-/A]AAAGTTTTTAAAAAG | 1130 |
rs141938724 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235736344 | GTTCTGAGTAGACTA[C/T]AGAAAGGGAGAAAGG | 1130 |
rs141958285 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235698423 | ATATCATAGTGGTCT[-/A]AAAAATGAGTATCTC | 1130 |
rs141971330 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235793829 | ACTTTTCTTTTTATT[A/C]TTTTTATTATTATTA | 1130 |
rs142010121 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235870288 | ATGAGCTATAACAAA[C/T]GAAGGTGTAAACAGG | 1130 |
rs142076781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235753746 | AGTATTTTGTGCCTC[A/G]TTTTCCTTATCTGTC | 1130 |
rs142086615 | snp | C/T | 1.65809e-05 | 0.00287926 | synonymous-codon | LYST | GRCh38.p7 | 1:235664590 | GAGATCCCCGTTCAC[C/T]GTCCAGAGTCTGAGG | 1130 |
rs142093128 | snp | G/T | 9.9519e-05 | 0.00705334 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773990 | CATCCTTCAAGAAGG[G/T]TCTATAGAAAATTAG | 1130 |
rs142099463 | in-del | -/AA | 0.436408 | 0.16659 | intron-variant | LYST | GRCh38.p7 | 1:235849797 | TTTTACAATAGCTCC[-/AA]AAAAAAAAAAAAAAA | 1130 |
rs142149764 | snp | G/T | 0.111928 | 0.208413 | intron-variant | LYST | GRCh38.p7 | 1:235720163 | CTGGTGACAGAGTGA[G/T]ACTCTGTCTCAAAAA | 1130 |
rs142149838 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235784809 | CTCCATCTGATTTAA[C/G]TATAGGTTCTGGAAA | 1130 |
rs142174951 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235783048 | GACTTCATCAACTAG[A/T]GAAACCACAGAGCTC | 1130 |
rs142181377 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235876485 | AATTTTTTGGATAAA[C/T]GAGGAAGCTGATGAC | 1130 |
rs142182628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235746998 | GTGACAAAGTAGAAA[C/T]CAGTCAATGAAAGTG | 1130 |
rs142186137 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235838174 | ACAGCAAGACTGCCA[A/G]CTGAGAGTGAGAAGT | 1130 |
rs142194685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873195 | AAACATCAGAAACTA[C/T]TTCCTTGAGATGACC | 1130 |
rs142208500 | in-del | -/ATG | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854116 | TTGGATTTTTATAGC[-/ATG]ATGATGATGATGATA | 1130 |
rs142223913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826977 | TGTGAGGTGTATTTG[C/T]CACTATTCATCTAAC | 1130 |
rs142230053 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235694834 | CCACAAGAGGCATCA[C/T]CTTTTTTTTTTTCTT | 1130 |
rs142237669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724817 | TACTAAGCAAATATC[C/T]TTTTAAATACATAGC | 1130 |
rs142248578 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235882024 | AGACGATAAATTTTA[C/T]GTTATGTATATTTAA | 1130 |
rs142258180 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235722312 | GGATTCTGAGCAGAG[A/G]AAAGATATGATCCAA | 1130 |
rs142260167 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235787494 | AGTTCTATTTTTTTT[A/G]AAGTGCTTGAAAAGT | 1130 |
rs142286350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879716 | GAAAGCTCTGAGAAT[A/G]GATCTAACTTCCTTT | 1130 |
rs142340829 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235815903 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACAAGG | 1130 |
rs142344106 | snp | G/T | 0.000430392 | 0.0146633 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788823 | AGGATTTATGTACTC[G/T]GCACCTTCTGGTCTG | 1130 |
rs142346840 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235829245 | TCCTGAAAATTCCAT[A/G]ACAAGTAAATGCTTC | 1130 |
rs142360521 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235730454 | CCACCAGCAGCTCTA[A/C/T]CTATATTAATAGATA | 1130 |
rs142364034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693283 | ATGTGTCACTGCGCT[C/T]CAGCTTGGGCGGCAG | 1130 |
rs142397962 | snp | C/T | 0.000181772 | 0.00953167 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793565 | CTTCTGAACATGTTC[C/T]TGAACTCATCAAAGA | 1130 |
rs142431334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682641 | CATAGAAATGTAGTC[A/G]GATGAAAGAATATAG | 1130 |
rs142479102 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235731556 | CATTTCCCATTTTGC[-/A]TTTTTTTTTTTTTTT | 1130 |
rs142487833 | in-del | -/TATT | 0.124837 | 0.216412 | intron-variant | LYST | GRCh38.p7 | 1:235843245 | ATTCATTAATTCCAA[-/TATT]TATTTATTAAGTAAA | 1130 |
rs142512930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235759896 | GCTGGGACTATAGGC[A/G]TGCACCCCACACCTG | 1130 |
rs142528836 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235802572 | ACTTCCCTCACCACC[C/T]AGTTACTAATACGAC | 1130 |
rs142544079 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235701305 | TTATTAATTTTCAGG[G/T]ATGTATTGTAAAATT | 1130 |
rs142572492 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235666154 | TGTTGCAGCATTATT[C/T]ACAATAGCCAAGAAG | 1130 |
rs142585971 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | LYST | GRCh38.p7 | 1:235845116 | ACCCTCTGAAGGAAG[C/T]GGATTGCTCCTGCAG | 1130 |
rs142608315 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661109 | AGAGCTTGTGATAAT[G/T]TACAGAAATGTTTGC | 1130 |
rs142612856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235757633 | CATCACTTTTTATCA[C/T]TGATTTTTTTGGGCA | 1130 |
rs142617094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235704961 | GTGAACCCCATGTAT[C/T]AGTGAACGGTCATTA | 1130 |
rs142633098 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235795303 | ATAAACGAAATGGTC[A/C]GGTGTATACAGGCTT | 1130 |
rs142689486 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235717295 | AGATTTGGAGACTGA[A/G]AACTGAAATAAATAT | 1130 |
rs142712419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740134 | CCCTCAGTGTACTTG[A/G]AAGTGTCTTAATACT | 1130 |
rs142715841 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235869365 | TAGTCTCAGCTAATC[C/G]AGAGGCTGAGGCAGG | 1130 |
rs142736134 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235678394 | TGGTGATGTTACCAA[C/T]GGTAATGGGCCCTAA | 1130 |
rs142762144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820005 | GTGTTACACCTTTAT[A/G]AAATTCCCCATAGAA | 1130 |
rs142773397 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857255 | GAAGCTATCACCTTA[A/C/G]AAATGGTTGTGGATG | 1130 |
rs142775666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235676612 | CCTACCTCCTCTGCT[C/T]GGCTCTCTGGGGTAC | 1130 |
rs142810791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235681775 | TCTCATCCTGTAACT[A/C]CTCATCACATTTGGA | 1130 |
rs142837703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235882887 | TCTCAATTTTACTGG[C/T]ACCCGAGAATCAGAT | 1130 |
rs142845103 | snp | C/G | 1.65026e-05 | 0.00287246 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810082 | TCATGTTACTGATAA[C/G]AGACAAGGCAGCTGG | 1130 |
rs142858690 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235857411 | TTCCTATATAAGGAT[A/G]TTGGGATTTGAAGAA | 1130 |
rs142866112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235765473 | ACTAGAATACAAGTT[C/T]GAATTCTCTGGCCTT | 1130 |
rs142880080 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235794505 | TCAAAGTATTTTTAC[A/G]TGCTTTATTTCAGCT | 1130 |
rs142881581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235783419 | TTTTATTTTAAAAAA[C/T]AGTTTTTCAATGAGA | 1130 |
rs142951434 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235717674 | ACATTTCAGTGAGTC[A/G]AACCAGGTCTGCTTA | 1130 |
rs142973884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850005 | TACCACTATCATTCT[C/T]CACAGAATTAGAAAA | 1130 |
rs142980448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235698261 | CATTTCTGTAAAAAA[C/T]CTGATTTTTAGTGAA | 1130 |
rs142982293 | snp | C/T | 4.94694e-05 | 0.00497316 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804594 | TAAAGGCTTTGCTAG[C/T]TGTGTTTCAATCACC | 1130 |
rs142983846 | snp | A/G | 0.000531729 | 0.0162967 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788752 | ACTTGGATCATCAAC[A/G]CTTTGGATCCCAGTG | 1130 |
rs143032387 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235840580 | GCAAGACCTAAACAT[C/T]GGTATTTTTAACAAG | 1130 |
rs143033869 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235691166 | CTTGTGATCCGCCCG[C/T]CTCGGCCTCCCAAAG | 1130 |
rs143063208 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | LYST | GRCh38.p7 | 1:235799089 | ATCACAAGGGTTCAC[G/T]AAGTGTCTAGCAAAA | 1130 |
rs143079247 | snp | C/T | 9.88614e-05 | 0.00703 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734592 | GCTGTGCCTAGCTCT[C/T]CTTCAGTCAATTCAC | 1130 |
rs143083554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235700727 | CATCACACAGAAATG[C/T]AGCAAACCAAACCTT | 1130 |
rs143085071 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235830692 | CCTGGATGGAAAACA[A/T]TTTCTCTTTTTAAGA | 1130 |
rs143096905 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235824005 | AAACTGTAGCCACAC[-/AG]TTCTAAAGGTCTGAT | 1130 |
rs143163582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235685318 | CTGCCTGGATCACTG[C/T]GGTGGCCTTCTCGTT | 1130 |
rs143182181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235773595 | ATGAGATCCTTAGAT[C/T]AGTCAAAAGTAGAAT | 1130 |
rs143217805 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235663928 | TTAAATACCTCTCTA[A/C/T]GAAAAATACAATCAC | 1130 |
rs143223086 | snp | A/C | 0.00188091 | 0.0306091 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805777 | TCCATCTTCTGTTGA[A/C]TAGTTCTGGCACCAT | 1130 |
rs143253866 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235680756 | GGCAGCTGCCACCAC[A/G]CCCGGCTAATTTTTG | 1130 |
rs143255816 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235704010 | GAACATGTGGTATTT[C/G]GTTTTCTGTTCCTGC | 1130 |
rs143260619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235802318 | CTTTTCCATTCTACT[C/T]ATTTTAAGTCCAAAG | 1130 |
rs143285898 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805983 | TTTTAGACTACCTAG[C/T]TCTGATGGTATGGGG | 1130 |
rs143291405 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235699567 | TCTTTAGAGTAGAAT[G/T]ATTTATATTCCTTTG | 1130 |
rs143310720 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235862325 | TCATTTTCCAAGGTT[C/T]CAGTTACCTGAGGTC | 1130 |
rs143356830 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235675598 | AACATGGTGCACCCT[A/C]ACTCCACAACCCTGA | 1130 |
rs143361104 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235668911 | ATAAAAATGTTTTCA[C/T]GACATTATTTTACAA | 1130 |
rs143389299 | snp | A/C/G | 6.59776e-05 | 0.00574326 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809102 | AACACCCGATAGGAT[A/C/G]TGGACACAAGTGCTG | 1130 |
rs143475165 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235775495 | GATGTATCTATAAAA[A/T]CCACATGTCCTGCCT | 1130 |
rs143485175 | in-del | -/T | 0.0759472 | 0.179459 | intron-variant | LYST | GRCh38.p7 | 1:235699579 | AATGATTTATATTCC[-/T]TTGAGTATATACCCA | 1130 |
rs143490489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235859769 | CATCTGTCCCCTTTG[C/T]GCCTTCCTGGGATTA | 1130 |
rs143495771 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235726333 | TAATTTTTATAAGTA[C/G]AGGCAGGGAATATAT | 1130 |
rs143516220 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235880220 | ACCACTTCCTCAATT[C/T]CAGAGAAGAAGGAAG | 1130 |
rs143539409 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235771225 | CAAATCTGAAAAGTA[A/G]TACCAAGATAAAATA | 1130 |
rs143594664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853296 | AAATTTCAGCATCGG[A/G]GGGTTAAGAATTGGC | 1130 |
rs143599230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719705 | AAAAAAAGAGTTGAA[C/T]CTGAAACTAAGCAAG | 1130 |
rs143601402 | snp | C/T | 8.24899e-05 | 0.00642169 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810396 | TGTCGTCTGCTTTTT[C/T]GAAAAACATTTACTT | 1130 |
rs143602388 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235823244 | ATTTCCACTGTGATC[A/C]CACTCTCACTACTCC | 1130 |
rs143618409 | snp | C/T | 0.000115313 | 0.0075923 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720748 | TACTGCATGAGATCA[C/T]TGAAGGATCGGCCAG | 1130 |
rs143632723 | snp | A/C/G | 6.59439e-05 | 0.0057418 | missense | LYST | GRCh38.p7 | 1:235697190 | TCTCCGTGGGGCTGG[A/C/G]TGAAGCAGACCACAG | 1130 |
rs143673470 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | LYST | GRCh38.p7 | 1:235693486 | TTCATGCTTCTCACA[C/T]CTCAAGGAGAAGGAG | 1130 |
rs143683082 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235778119 | TATATATATATATAT[A/T]TATTTTTGTAGAGAC | 1130 |
rs143685163 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235714176 | AACCACAGCAAACAA[A/G]GATGGCTTAAACATT | 1130 |
rs143691532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235870833 | ATTAAGAAAATTTTG[C/T]TGAAAATTCAAATAA | 1130 |
rs143696500 | snp | C/T | 0.000148447 | 0.00861404 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777149 | CAGTAGGTTGGAGAT[C/T]CTTTAGATGATGAGG | 1130 |
rs143697353 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235773255 | GCCTGGGGGTGGAGG[C/T]TGCAGTGAGCCAAGA | 1130 |
rs143706691 | snp | C/T | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777104 | CAGTTCCACCAATTT[C/T]GTGCAGAATGCCTTG | 1130 |
rs143706899 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235864869 | GGGAAGTCGAGGCTG[C/T]AGTAGGTTGTGATCA | 1130 |
rs143713214 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235700937 | CAATATGTCAGGTGA[C/T]AGAAGTGCTATACAC | 1130 |
rs143723809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837998 | AATGAGTAGGCAAAA[C/T]GAAGAAGACCAACAT | 1130 |
rs143748446 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235839832 | AAAATGAAATAAAAT[A/G]AAATAAAATAAAATA | 1130 |
rs143779703 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235707207 | TGGCTTTCCTCCTAA[A/C]CCCCTTCACCCTATT | 1130 |
rs143806924 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235856184 | TAGACTTGTATAAAG[-/A]AAAAGGGTTAAAGTT | 1130 |
rs143820398 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235697447 | TAGCGTATAGAAATA[C/T]TTGTCCCTTATTTGA | 1130 |
rs143828167 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235718416 | AACATGATCTCAGCT[C/T]ACTGCAACCTCCGCC | 1130 |
rs143853773 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235682505 | ATGCAGGAGAGGCCA[G/T]GAGCCAGGTGGGAGA | 1130 |
rs143857674 | snp | C/T | 8.26262e-05 | 0.006427 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773950 | CTCTCCATTCTCATT[C/T]ATATAAATAATATCT | 1130 |
rs143888478 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235693794 | CTTACTCTATTCATG[C/T]TCTGAGACACCTTTT | 1130 |
rs143888717 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235748803 | ACTGCTGAAGAAACT[G/T]TGGTTCCAAGTCATG | 1130 |
rs143892570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840011 | TACCTACCTTTTCTT[C/T]GAATTTTAGGAACTC | 1130 |
rs143922170 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235744752 | AAAAAAATACAAAAA[G/T]TAGCCGGGCATGGGG | 1130 |
rs143925541 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235837484 | AATACAAAAATTAGC[C/T]GGCATGGTGGTGCAC | 1130 |
rs143968895 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805955 | CTAATTTACCTAAAC[A/T]GTCAGCACTCTTTTT | 1130 |
rs144005676 | snp | A/G | 3.31274e-05 | 0.00406972 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762769 | TATTACCATAAATCC[A/G]GGGCTCATAAGGGAC | 1130 |
rs144020505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751419 | TACTAATTTTTTAAT[G/T]GAACTGATTTTATGT | 1130 |
rs144021463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695355 | AAGGATGCAAAACTC[A/T]GGAACTGCCTGTGGA | 1130 |
rs144035072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697775 | ATCTCAAATAGATAC[A/G]TGATGAGTGAAAGGG | 1130 |
rs144039032 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235841950 | GGAAAGTAGTGATGA[A/C]AGACAAAATAATTTA | 1130 |
rs144045821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838440 | ATGTAGACTCTATAG[A/G]TAGAAACTGGGTTAT | 1130 |
rs144072811 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235677974 | TTTAATGATGTTATA[A/G]TATTCTATACAGTTA | 1130 |
rs144084470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820460 | CTGCAACCTCCACTG[C/T]CCAGGCTCAGGCGAT | 1130 |
rs144184250 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235674918 | ATTGTTATCAGTGTA[C/T]TCATTCTTGTAAGTT | 1130 |
rs144185016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871896 | AGATTTCTACATGTC[A/G]GGGAGGAAATGTTTC | 1130 |
rs144185276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235745722 | AAAAAAAGGAACTAT[C/T]GATATATGCAACAAC | 1130 |
rs144218323 | in-del | -/ACAC | | | intron-variant | LYST | GRCh38.p7 | 1:235666582 | TAAATATACATTGAG[-/ACAC]ACATGCACACACACA | 1130 |
rs144236405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235814248 | TATGGAGTCTGAGAC[A/G]TCTATGCACTATCCT | 1130 |
rs144247734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680235 | CTCTTGTTGGCCATC[A/G]GCCATGATCATAGTT | 1130 |
rs144248714 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235670835 | TGCAAGAAATCTCTA[A/G]TAAGAGAGGTTGAAC | 1130 |
rs144252883 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235710569 | TGATAGGAAATGATA[C/T]GATATACGCTGTAAA | 1130 |
rs144261004 | snp | C/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806566 | TGCTGATGATGAAAA[C/G]AAGTACCCACATGTA | 1130 |
rs144275846 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235729737 | TTATTTTACCTAGTA[A/G]AAGATTTCTGCAAAG | 1130 |
rs144286603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825683 | AGAGAAACAAACTAA[A/G]GAAGACATAAATAGA | 1130 |
rs144296940 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235668251 | TGGATGATATCCAAT[A/T]AATAGTCAAAATTTT | 1130 |
rs144300503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235821883 | ATAATACTCTTTGTT[A/G]AGACTCCAGAAAGAC | 1130 |
rs144307860 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788760 | CATCAACGCTTTGGA[G/T]CCCAGTGAAATTATA | 1130 |
rs144312080 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235882971 | TATTCTCCCTCCTCA[A/C]ATACTCTTCCCTGCG | 1130 |
rs144314724 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235719087 | GCAGTGGTGCAATCT[C/T]GGCTCATCGCAACCT | 1130 |
rs144316471 | in-del | -/ATAT | 0.00792067 | 0.0624307 | intron-variant | LYST | GRCh38.p7 | 1:235805629 | ATATATAACACAATA[-/ATAT]ATATATTACATATAT | 1130 |
rs144353932 | in-del | -/AAG | | | intron-variant | LYST | GRCh38.p7 | 1:235726576 | TACCAAATGTTATAT[-/AAG]AAGAACCAACATTAC | 1130 |
rs144362985 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235879877 | AAGTAGCTGGGATTA[G/T]GGGCATGCGCCACCA | 1130 |
rs144378548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235722127 | TGAATGCAAAGTCCC[C/T]GAGGCACTGGTGTGC | 1130 |
rs144382506 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235824877 | CTACAAAAATTAGCC[A/C]GGTGCAGTGGCAGGT | 1130 |
rs144384971 | snp | C/T | 9.90589e-05 | 0.00703702 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733882 | CTTTATTCACTCCTT[C/T]TTCAGTTTCATATTT | 1130 |
rs144415748 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235875051 | TTTTAACACGATCCC[C/T]GGGTGATTTATATGT | 1130 |
rs144446737 | snp | C/T | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830307 | AAGGGTTGCCATGTG[C/T]GTCTCCTCCTCTTCT | 1130 |
rs144446792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683825 | AACCTCACAAGCTCA[A/G]GGTCAGAACCACAAC | 1130 |
rs144451594 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235785229 | AGGCCTTCCCTGATC[C/T]ACCCATCGTAAGTGT | 1130 |
rs144475533 | snp | A/G | 0.00324127 | 0.0401264 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731081 | ATTTGGAATAGTTAA[A/G]TAACATCTCTGTAAA | 1130 |
rs144483136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235770968 | AGATAACCTTCCCTT[C/T]ATCTTATTATCCTAA | 1130 |
rs144524632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841484 | CTTAAAATCATCATG[A/G]TGAGAGTATTTCCAT | 1130 |
rs144597913 | snp | A/G | 0.00302706 | 0.0387861 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734531 | TGATGCACTGGGAGG[A/G]ATGCACTTGTGACCA | 1130 |
rs144619475 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235696890 | CAAGTTCCTCCTCTC[A/T]TTTCAAATAGCACTG | 1130 |
rs144636985 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661549 | AAGCATACATGGCCA[C/T]GTGCTTTCTCTCGAA | 1130 |
rs144646479 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235789104 | AATAACTGAGGACAA[C/T]TGTGGGCGTAACCAG | 1130 |
rs144648929 | snp | A/C/T | 0.00438524 | 0.0466503 | intron-variant | LYST | GRCh38.p7 | 1:235795293 | TCTTCTCTAAATAAA[A/C/T]GAAATGGTCAGGTGT | 1130 |
rs144664809 | snp | C/T | 6.62888e-05 | 0.00575674 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800934 | CAAAAAACTCTCAAA[C/T]ACATGGGCAAGCACA | 1130 |
rs144728424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853782 | ACTCAGGCATAGGGC[A/T]GCCAGGCAAAATTTT | 1130 |
rs144791213 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | LYST | GRCh38.p7 | 1:235850869 | TAATCAAAAAATCAA[A/G]AAACAGTAGATGTTG | 1130 |
rs144829166 | snp | A/G | 1.68049e-05 | 0.00289865 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788707 | AATCAATACCGAAAG[A/G]TAAGAGTGGCATTGT | 1130 |
rs144829441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235776511 | TTTTTACTAAAGTGA[A/G]ACTGTTGGTGCTCCC | 1130 |
rs144836595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687483 | ATGTAAACAGAGGTA[C/T]TGCTTCTAATAGTTC | 1130 |
rs144840340 | snp | C/T | 4.94735e-05 | 0.00497336 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806009 | TGGGGTCACTTTTTA[C/T]AGCCAAAGATAATAA | 1130 |
rs144856366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235760293 | AGATTATATTTGTGA[C/T]GCACCTAGCATAGAG | 1130 |
rs144861545 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866229 | ATACCGGAGACAGAC[A/G]GCAGATGTCTCAGGG | 1130 |
rs144861708 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235812111 | ACATTTAAAGTTTCA[G/T]GTACTTTATAGACAT | 1130 |
rs144862823 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828992 | GGTAGACTGCTTGAG[C/G]TCAGGAGTTTAAGAT | 1130 |
rs144878739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709588 | AGAAAAGGAGAAAAC[C/G]ATTGCCTACTAATTC | 1130 |
rs144888090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235706711 | TCACCAATGAAACTA[C/T]ATTATTCTCCTTTTT | 1130 |
rs144899101 | snp | C/T | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741447 | GGGCTGAGACAGTCT[C/T]GTAGTATTTCCTGAT | 1130 |
rs144919024 | snp | C/T | 3.29886e-05 | 0.00406118 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809093 | AATGTTATGAACACC[C/T]GATAGGATCTGGACA | 1130 |
rs144931121 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235856400 | TTCTCTTTAGGATCT[C/T]AGGCAAGGTGCTTAA | 1130 |
rs144953631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670222 | AGTTTAAGTCTTAGC[C/T]AATAATTGGGTTAGA | 1130 |
rs144960669 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235791476 | AGTTGTATATGTGGT[G/T]TCCCCTTCACCCCTA | 1130 |
rs145008679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734426 | AAAAAGTAGTGTCAA[G/T]CATTCTTTATCTATG | 1130 |
rs145055043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235763687 | TGGAGTTGAACTCCT[A/G]GCCTCAAGTGATCCA | 1130 |
rs145069394 | snp | A/G | 3.31235e-05 | 0.00406948 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766135 | ACGTAAGTATTAGTA[A/G]GAGGGTGAACTGCTA | 1130 |
rs145069705 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235678736 | TCCTATTTCTTCTGT[C/G]TTGTCAGAAGTTACT | 1130 |
rs145077787 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724128 | TTGTGAACTTCTTTA[A/G]TTTCTTCATATGTCC | 1130 |
rs145080654 | snp | C/T | 0.000197772 | 0.00994217 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759421 | AGAATTTTGTTTCTT[C/T]GATTGGGTGGCAACA | 1130 |
rs145099272 | in-del | -/A/AA | 0.0876345 | 0.190099 | intron-variant | LYST | GRCh38.p7 | 1:235773317 | GTAAAACTCCATTTC[-/A/AA]AAAAAAAAAACAAAA | 1130 |
rs145124875 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235878286 | CACCCTGAGTGATGA[A/G]GGAGTGGCTTGTGGC | 1130 |
rs145136281 | snp | A/G | 8.23621e-05 | 0.00641672 | synonymous-codon | LYST | GRCh38.p7 | 1:235686991 | GGCTGTGATGACACC[A/G]CATTTGCTTCCAGTA | 1130 |
rs145145263 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235719179 | ATGTGCCACCACGGC[C/T]GGCAAATTTTGTATT | 1130 |
rs145149520 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235786750 | TCATGTCCTTTGTAC[A/G]GACACGGATGAAGCT | 1130 |
rs145150526 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | LYST | GRCh38.p7 | 1:235839105 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCACCT | 1130 |
rs145162897 | in-del | -/ACAC | 0.485255 | 0.0845871 | intron-variant | LYST | GRCh38.p7 | 1:235857743 | CAAACATATGTAAAT[-/ACAC]ACACACACACACACA | 1130 |
rs145183349 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235836439 | CTGTTTCAGATAGGA[C/T]GGACAAGGAAGGTCT | 1130 |
rs145200338 | snp | A/G | 0.00150702 | 0.0274088 | intron-variant | LYST | GRCh38.p7 | 1:235830438 | AGCTATAAAATAAGT[A/G]TTACAAAAAAAAAAG | 1130 |
rs145207504 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235872455 | GAGTTTGATCTCGTG[C/G]TAATAGACCGAGGGG | 1130 |
rs145208920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835474 | TCTGTTTCTCTTATC[A/G]AGGGACATTTTCTAG | 1130 |
rs145244254 | in-del | -/A | 0.0314385 | 0.121371 | intron-variant | LYST | GRCh38.p7 | 1:235852212 | GGCTTTTAACTACAG[-/A]ACCCTACAGAATCTT | 1130 |
rs145282807 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235741902 | ACAAAATGTGGTATA[C/T]ACATACAATGGAATA | 1130 |
rs145284556 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | LYST | GRCh38.p7 | 1:235691119 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 1130 |
rs145287438 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805793 | TAGTTCTGGCACCAT[A/G]AAGACAAATGGCCAG | 1130 |
rs145292565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235783847 | ACCTTATTTTAAAAG[A/G]CCTCTTCAAATGTAT | 1130 |
rs145298434 | snp | A/T | 0.000513887 | 0.0160212 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808989 | AGGATATTCAATATA[A/T]GCTGCTGAAAATTTT | 1130 |
rs145299164 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235833926 | ACTTAAAACCTCCAG[A/G]TAAATCACAAGTTAA | 1130 |
rs145304441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815809 | ACAAATGGAGAAACA[C/T]TCCACATTCATGAAT | 1130 |
rs145319701 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713585 | CAATGTCTAGCAACA[C/T]TTTTGATTCTCACAA | 1130 |
rs145341273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844529 | TGAAATAAGCAAGTT[C/T]AGAAGATACATAGCC | 1130 |
rs145363852 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | LYST | GRCh38.p7 | 1:235864750 | CAGCCTGGGCAACAA[C/T]GGCGAAACCCCATCT | 1130 |
rs145373322 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | LYST | GRCh38.p7 | 1:235693123 | GATCGAGACCATCCT[G/T]GCTAACACGATGAAA | 1130 |
rs145374393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738509 | GGACTCAGCCCAATT[A/C]CGTTACCCAATGGGG | 1130 |
rs145412647 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235675574 | TTGTTTCTAACAACT[C/G]TGTGCCAGAACATGG | 1130 |
rs145439907 | snp | C/T | 3.3157e-05 | 0.00407154 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830389 | TCGGTCAGAAATTCA[C/T]GTGCCAGTGAGTTAC | 1130 |
rs145489492 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235849226 | CATACGTAAGTCAAT[-/AA]AAATGTGATACACCA | 1130 |
rs145533752 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235701909 | ATAATTTATATCCAG[C/T]GTTCTGTCTTACATA | 1130 |
rs145553827 | snp | C/T | 0.000959359 | 0.0218806 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802937 | TCGCCATCTTCAGGA[C/T]TGCTTTCACTATCTG | 1130 |
rs145553837 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235676915 | GCATAAGCTGAGGCC[C/T]AAATTGATGCACTCA | 1130 |
rs145574735 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235818631 | ATAAAAATGTACATG[C/G]TCTTTTAAAAAAAAA | 1130 |
rs145611231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675471 | TTACGATCGGTCGGT[C/T]GGACGCAGGCAGCAC | 1130 |
rs145649269 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235758481 | TCAGCACTAAGACCT[G/T]CATTATAATTACCTG | 1130 |
rs145657596 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673809 | GACAAAACCAAAGTA[A/G]TTATAATAAAAGTCA | 1130 |
rs145665074 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235815734 | AGCTAACCAGGAAGG[G/T]GAAAGATTTCTACAA | 1130 |
rs145666408 | snp | C/T | 3.30256e-05 | 0.00406346 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806105 | TATCTCCCTCCTTTT[C/T]TCCTTGCTCCTCTTT | 1130 |
rs145682413 | in-del | -/AC | 0.0494327 | 0.149241 | intron-variant | LYST | GRCh38.p7 | 1:235857705 | CAGGTGTATATATAT[-/AC]ACACACACACGTATA | 1130 |
rs145695494 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | LYST | GRCh38.p7 | 1:235685225 | GTCCTTCTTCTGTGG[A/T]CCTCTATCCTGGGTG | 1130 |
rs145717272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676456 | GATTCACAGCAATCA[A/G]TGACAGGGGATCACT | 1130 |
rs145797805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235679736 | TCCAGGGTTCTCCCA[C/T]GCAACTCATTTTCAT | 1130 |
rs145820873 | in-del | -/ACAT | | | intron-variant | LYST | GRCh38.p7 | 1:235857784 | CACACACACACACAC[-/ACAT]ATATATATATAAAAT | 1130 |
rs145821404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821513 | CTCTATTCGAAGCTT[A/T]ATTTGTTTTTAGACC | 1130 |
rs145853601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235873228 | TCCAACCAACTAAAA[C/G]TGTTAAAAACAACTG | 1130 |
rs145868256 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235780262 | ATTTAAAATTAGCCC[A/G]GTGTGGTGATGCATG | 1130 |
rs145878466 | in-del | -/A | 0.182614 | 0.240747 | intron-variant | LYST | GRCh38.p7 | 1:235704722 | GTTTACTCTATTGAT[-/A]GTTTTTTTTCCTGTG | 1130 |
rs145880647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235831221 | CACCTCCCTTCACCC[A/G]CTTCAGGGGGAAGCC | 1130 |
rs145882461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235776318 | CTGATATGCTTCTTA[C/T]TGCAAAATTAATCAA | 1130 |
rs145882998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235839452 | GTGATCCACTGCACA[C/T]GACCATTTGGTTTCA | 1130 |
rs145890993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748340 | ACAAGTAAAAAAATA[A/C]ATTTAAAAGTATATA | 1130 |
rs145892183 | snp | A/G | 0.000560667 | 0.0167338 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806190 | GAAACCACCAAGCCT[A/G]TAAAACTGTTTCTGG | 1130 |
rs145895529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735355 | GTGAAAAACTCGCAA[A/G]CCCCACGCAGACAAT | 1130 |
rs145973468 | snp | G/T | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787204 | ATGCTTCCTACCTCT[G/T]TCCAGAGACCCATAT | 1130 |
rs145985034 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235800691 | TTTTCTATGCTACTT[A/T]AGAAAACTATGGAAT | 1130 |
rs145989763 | snp | A/G | 0.121022 | 0.21416 | intron-variant | LYST | GRCh38.p7 | 1:235701508 | TGGCGGGCGCCTGTA[A/G]TCCCAGCTACTCGGG | 1130 |
rs146022952 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720756 | GAGATCATTGAAGGA[C/T]CGGCCAGCATGTTTG | 1130 |
rs146027359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235721070 | ACTGAGATTCAAGTC[C/T]AGGTTGTCCTCCAGA | 1130 |
rs146029844 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235668739 | ACTCCATATAAACAA[G/T]CATTATATTATTTCC | 1130 |
rs146031306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665528 | GAGGCAGAAGAATCA[C/T]TTGAACCCAGGAGGT | 1130 |
rs146041973 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235807018 | AGTATCTAAAAAGAA[A/G]AGATTGCCTGTCCCA | 1130 |
rs146091043 | snp | C/T | 0.00179721 | 0.0299228 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759561 | AACGCAGCATATGGG[C/T]GGCCATCTGTTGTGG | 1130 |
rs146106811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235826196 | GGTAAGAATGAAACA[C/T]AGTACAACTACTTTG | 1130 |
rs146107208 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235832014 | CCATCAAGACCATTC[A/G]TGCCACAGCACTTAA | 1130 |
rs146107518 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235777561 | GATTCCAGCTTTGTT[C/T]GGTTTAGAATATATA | 1130 |
rs146112420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688618 | TGAAGGCACACAGCC[A/G]TCAGGACTCTAGACT | 1130 |
rs146127165 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235829189 | GCCTGGGCGACAGAG[C/T]GAGACTCTGTGTCTC | 1130 |
rs146154938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235691332 | AGAAACTCAAGTTTG[A/G]AGAGATTAAGTTACT | 1130 |
rs146158562 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235688974 | TGGCAACAGAGTGAG[A/G]CTCCGTCTCAAATAA | 1130 |
rs146164878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782945 | GTCTCTTTTGCTTCA[C/T]GGATAACGGTGAAGG | 1130 |
rs146207390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724935 | ACTCTGGTTGCTCTG[C/T]TGTATGTGTCTGCAT | 1130 |
rs146209065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235807872 | TTAATAATCCCATTA[A/G]TGCCTCTGCCTCAAT | 1130 |
rs146215689 | snp | A/G | 0.000329946 | 0.0128399 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733647 | GTGATATCTGCAGCT[A/G]TTTTAGATATATCCT | 1130 |
rs146233251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669422 | TTGCAAAACTCCCAC[A/G]TTTTCTGCTGGCAGA | 1130 |
rs146235631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750880 | TCCCTAACTCCTGAT[A/G]TAGATTGCCCTGTTA | 1130 |
rs146274816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674622 | GCTAACTATACTAGG[A/G]ATGCCATTAAAGGAA | 1130 |
rs146335682 | snp | C/T | 0.000297089 | 0.0121843 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806411 | CTGCTTCTTTACTTA[C/T]GCATAAAAAAGCCAC | 1130 |
rs146341184 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235871716 | CCCTACTCTGTAATT[C/G]AGTAGTCTCTAATAA | 1130 |
rs146354628 | snp | A/C/G | 9.8867e-05 | 0.00703027 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810215 | GTCAAGTTTAGCTTT[A/C/G]GGGTGGTCTTGTTTA | 1130 |
rs146369716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876603 | AGATTTTATTTAAAT[C/T]CTGATTTTTTGTTCC | 1130 |
rs146393636 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235724363 | ATAAAATTTAGAAAT[-/A]AAAAAAATAGGCTTT | 1130 |
rs146393963 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235851198 | GTGTGTATATATATA[-/AT]TATATGATGAAATAC | 1130 |
rs146395688 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235728414 | TATGCAAAATGCATA[C/T]GTGCTCAGTGCTAAA | 1130 |
rs146409051 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235747682 | ATGATTGTAATTCAG[C/T]GGTATGATAATACAC | 1130 |
rs146419389 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235838522 | TTAAGTATAATATTT[G/T]AAAATCTTTAAAAAT | 1130 |
rs146423463 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235835992 | GCCCCAACGATATTC[A/G]TAGAATTTTTATATC | 1130 |
rs146447697 | snp | C/T | 0.030665 | 0.119967 | intron-variant | LYST | GRCh38.p7 | 1:235699466 | TATATATTTTCTTTA[C/T]CTAGTCTATCATTGA | 1130 |
rs146457386 | snp | A/G | 0.00011532 | 0.00759255 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702900 | ACGGGGAGTCTGCCC[A/G]TAGGTTTTTATCATG | 1130 |
rs146507095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845215 | CTGAACACACACCCC[A/C]ACTGGAGAAGCTGAA | 1130 |
rs146513322 | snp | C/T | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805805 | CATGAAGACAAATGG[C/T]CAGAAGGGCTTCCAA | 1130 |
rs146535813 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235822451 | TATATAGGGCATATG[C/T]GGAGCAGATAACCTG | 1130 |
rs146553619 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235816677 | TACTCTATGAGGCTA[C/T]AGTAACTAAAGCAGC | 1130 |
rs146563137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235749049 | CAGTAAAGAGAACGG[C/T]TTGAGTCTTTGAAGG | 1130 |
rs146563460 | in-del | -/TTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235878294 | TGATGAGGGAGTGGC[-/TTTT]TTGTGGCAGAGCAAC | 1130 |
rs146571345 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235684119 | AAGTGTGTCATGACC[G/T]CAAAACTAAAAGAAA | 1130 |
rs146591126 | snp | A/G | 0.0124264 | 0.0778382 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766255 | TCTCGGGGCATGGGT[A/G]TGAGTTGCCCCTCTT | 1130 |
rs146596853 | snp | G/T | 1.65231e-05 | 0.00287424 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781989 | AAAAACTCTTCTTGG[G/T]ATGATAAACAATGGC | 1130 |
rs146619167 | snp | A/G | 0.197393 | 0.244402 | intron-variant | LYST | GRCh38.p7 | 1:235665542 | ACTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA | 1130 |
rs146652525 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235796897 | TAATACATTAGCCTT[C/G]AGGGGAATACAAATC | 1130 |
rs146688735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665919 | GGGGAAATACTCTCA[C/T]ACTGATAAAGCGGTT | 1130 |
rs146691144 | snp | C/T | 0.000328677 | 0.0128152 | intron-variant, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747264 | GAAGGGCATCGGAAG[C/T]TGACCATAGGAACCA | 1130 |
rs146707746 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661604 | GAATTATATTTTATA[C/T]GGTTTTTAAGCAGAA | 1130 |
rs146708664 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235740951 | GAAGTGATAAACTTT[A/G]TACACTCTGAAATTC | 1130 |
rs146710086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802389 | AAAGACAAATTGAGC[A/T]GTGGTAAACTAAGAA | 1130 |
rs146766703 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866258 | GGGATCCCCTGGAAA[C/G]AGAGGCTCTCGCCCA | 1130 |
rs146774268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773356 | AAACAAACAAAAAAA[C/T]GAGTATATGCTTCTA | 1130 |
rs146775996 | in-del | -/AA | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235781538 | ATTTGATATTTGTAT[-/AA]GATATAATAAAATTA | 1130 |
rs146788046 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235858302 | TGTAAAATGTTGATA[C/G]TAATATGTGAAACAT | 1130 |
rs146811128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235718493 | TCTCGAACTCCTGAC[A/G]TCAGGTGATCTGCCT | 1130 |
rs146830600 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715081 | GAATAAATAGAATTC[G/T]TTTTCCTGTAGTTTG | 1130 |
rs146872810 | snp | C/T | 0.000131959 | 0.0081217 | synonymous-codon | LYST | GRCh38.p7 | 1:235709181 | CTGACAGATGTTCTG[C/T]GACACGTAGTCAGAC | 1130 |
rs146909580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235702593 | CACAGCATTTACCTC[A/G]CACAGGATTCTGCTT | 1130 |
rs146918392 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235874262 | ATTGCAGGATTGATC[G/T]GTTATTTCAGACCTT | 1130 |
rs146951440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827775 | AATATTTAACTTATG[A/C]CCTAAATAATTTTAG | 1130 |
rs146967953 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235824492 | TGAGGACACTGTGCT[C/G]TGGAGCAATTAAGTG | 1130 |
rs146974130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774787 | GTTTGATTAACTATA[A/C]ACTAATAAGTTTCCT | 1130 |
rs146990900 | snp | A/G | 0.000132398 | 0.00813519 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777105 | AGTTCCACCAATTTC[A/G]TGCAGAATGCCTTGA | 1130 |
rs147011294 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235778832 | AATCAGAAATCTGAC[A/G]TTGCACCCTGACATG | 1130 |
rs147015542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235690201 | AGATTACTGATGACA[A/G]CAATGAGTTAAATCT | 1130 |
rs147065243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799146 | TAAGTAAATGAATGA[G/T]AAGAGAAAGCTTTTC | 1130 |
rs147094885 | snp | G/T | 1.69461e-05 | 0.0029108 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753065 | TCTAATCCATTCAGG[G/T]CTGCTACTGTATTAC | 1130 |
rs147095101 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235667468 | AACTGAGAAATTATG[A/G]TCAGGAGGAATGAGC | 1130 |
rs147117876 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235671677 | ACTTACTTGGCATGT[G/T]TAAGGAATAACAAAG | 1130 |
rs147128669 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235861357 | AGCAGTTAGACCTGG[A/G]AAGCCTTCAACATTT | 1130 |
rs147133264 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235771282 | ACAAAAAAAGAAAAA[C/T]GAGACTTAGTTCAAA | 1130 |
rs147144821 | snp | C/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235855422 | CATTTAAGGCACTAC[C/G/T]GAAACACCTTAAAAA | 1130 |
rs147166132 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235716208 | AATGCGTAGCTATTG[C/T]GATTTTTGAATTTCC | 1130 |
rs147169658 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235710154 | TCTGTCTACTTTTTG[A/G]TCTTGTAAAAACAGT | 1130 |
rs147215613 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235789166 | CCAAGCTTCTTTTAT[C/T]AACTATGACTTCACT | 1130 |
rs147220685 | snp | C/T | 0.000643304 | 0.0179231 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808505 | AATCTGAAGCACGTC[C/T]TGAGGCAAGCACTGG | 1130 |
rs147221131 | snp | C/T | 0.00150706 | 0.0274091 | missense | LYST | GRCh38.p7 | 1:235664574 | AGTGGACATGTCCAA[C/T]GAGATCCCCGTTCAC | 1130 |
rs147231857 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235838078 | CAGAGAATACGAGTA[C/T]AGATGTAGGAAGATT | 1130 |
rs147232955 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235837580 | TGCAGTGAGCTGAGA[C/T]TGAGCCACCGCATAC | 1130 |
rs147237804 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235744774 | GGCATGGGGTGCACA[C/G]CTGTAGTCACAGCTA | 1130 |
rs147249480 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235833266 | ACGGTATTTTCTTTA[A/C]ATTTTTTCTAATATT | 1130 |
rs147271107 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235697969 | CCATTTGGCTGCCCA[A/C/T]GAACGGTAATGAAAA | 1130 |
rs147343437 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235717579 | CTTTTGGCTGAGGAA[A/C]CATCTGGTCTGGCAC | 1130 |
rs147355753 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235814647 | ATGCCCCTTAACTAA[C/T]GGCTTTAATGGAGTG | 1130 |
rs147356085 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235869388 | GAGGCAGGAGAATAG[C/G]GTGAACCCGGGAGGC | 1130 |
rs147379173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678480 | GGTGCTCTGAGGGCC[A/T]CACTGGCTCACGGAT | 1130 |
rs147426732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739349 | TGGATGTTTACCGTG[C/T]GTTATATAAATAACT | 1130 |
rs147428398 | snp | A/G | 1.65304e-05 | 0.00287488 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773917 | GATTATAGCATTAGA[A/G]TCTACATCCAACTTA | 1130 |
rs147431549 | snp | C/T | 6.62394e-05 | 0.00575459 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766133 | AAACGTAAGTATTAG[C/T]AGGAGGGTGAACTGC | 1130 |
rs147433918 | snp | C/T | 0.000477992 | 0.0154521 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810126 | TCAGTGTTTGACCCC[C/T]GTCTTGGAATAATCT | 1130 |
rs147446128 | in-del | -/GCCCTCGC | 0.135484 | 0.22223 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866689 | CGCGTCAGGCCGAGT[-/GCCCTCGC]GCCCTCGCGCCCTCA | 1130 |
rs147450475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235794167 | TGAAGATTAATTAGC[C/T]ACAAGTAAACTAAGG | 1130 |
rs147477424 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235744591 | CTGTTGCACAGAATG[C/T]ATATTAGAAAAGTGG | 1130 |
rs147480311 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant | LYST | GRCh38.p7 | 1:235663954 | ATCACAAATTGTATT[C/T]TGAAGCATAAGAGGG | 1130 |
rs147480497 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235668204 | TATACATACATAGAC[-/AT]ATATATATATATTTT | 1130 |
rs147486209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737295 | TGATTATGTTAATGT[C/T]AGGAACCAAGATATC | 1130 |
rs147531245 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | LYST | GRCh38.p7 | 1:235710754 | GTGGAAGTGATGCTG[C/T]GTGGCTGCTAAGAAC | 1130 |
rs147536126 | snp | C/T | 8.30186e-05 | 0.00644223 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746476 | TCATTTGCCACTGAA[C/T]GCATTTTCATCAGAA | 1130 |
rs147539199 | snp | A/C | 0.000116197 | 0.00762135 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741575 | GAAGGTCTCCTTACA[A/C]GACCACAGAATTTTA | 1130 |
rs147554258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706170 | CTTGCATTTATTTTA[C/T]ACTTGATGGAGTTTA | 1130 |
rs147554343 | snp | C/G | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806495 | GTCTCTTTGGATAAG[C/G]TTCTTTGAGGCCAGC | 1130 |
rs147602194 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235690250 | GTGTATTTTGACAGG[C/T]AGAATGTATTGTATA | 1130 |
rs147604420 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | LYST | GRCh38.p7 | 1:235778905 | GAGTTTGACTCTTGT[G/T]GCCCAGGCTGGAGTG | 1130 |
rs147620801 | snp | C/T | 0.000324987 | 0.0127432 | intron-variant | LYST | GRCh38.p7 | 1:235830456 | ACAAAAAAAAAAGAT[C/T]AGGAAAACAAATACA | 1130 |
rs147624736 | in-del | -/AACT | 0.0425829 | 0.139564 | intron-variant | LYST | GRCh38.p7 | 1:235847633 | AAGAATTCACCAATC[-/AACT]ATCTATTGCCTTCAG | 1130 |
rs147653704 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235784132 | CAATCCTTCTGCCTC[A/G]GCCTATCAAAGTGCT | 1130 |
rs147708222 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235755966 | ACCTAATGCTGAGAG[A/G]GAAAAAATCCGTAAA | 1130 |
rs147712066 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235672038 | CTAATAGCTTGGATA[C/T]AAGGAGAAAGAAGGA | 1130 |
rs147712474 | in-del | -/AACACAATATCATGCA | 0.084364 | 0.187256 | intron-variant | LYST | GRCh38.p7 | 1:235724629 | TGACATGTATCCACC[-/AACACAATATCATGCA]AAATAGTTTTATTGC | 1130 |
rs147724454 | snp | A/G | 8.2392e-05 | 0.00641788 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810230 | GGGGTGGTCTTGTTT[A/G]GGAAACGATGTTAAA | 1130 |
rs147756847 | snp | G/T | 0.00851663 | 0.0646976 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759371 | CTGATGAATGCGTCC[G/T]CTTTGCCTTTTTTCA | 1130 |
rs147761755 | snp | C/T | 0.000379028 | 0.0137612 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759398 | TTCAGTGTGTCGGAA[C/T]TCCCCAAAGAATTTT | 1130 |
rs147762075 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235675181 | TCTTTCTTGCTCTGT[A/G]AACAGCCCCCACCCT | 1130 |
rs147791378 | snp | C/T | 0.00236038 | 0.0342727 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759071 | ACAAGACTTGGCCAA[C/T]GGCCAACAGCTGCAG | 1130 |
rs147794568 | snp | A/C | 4.98401e-05 | 0.00499175 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808878 | TCTTCTAATTGGGCT[A/C]GTTGGTCAGAGTCAA | 1130 |
rs147812111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235725572 | CTGCCATCATATAGA[C/T]TTAGGTTAAATCCAT | 1130 |
rs147820240 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885499 | TCATAACATCAGGTG[C/G]AGCCCAGAACAATGA | 1130 |
rs147821562 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827110 | GGCTCACACCTGTAA[A/T]CCTAGCACTTTGGGA | 1130 |
rs147830213 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235880009 | CCCAAAGTGCTGGGA[C/T]TACAGGTGTGAGCCA | 1130 |
rs147856240 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884842 | CTGAAGCCCAGGCCA[A/G]AGCGCAGTTGTGTGA | 1130 |
rs147862418 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235731450 | ATTTTTTAAAAGATA[C/T]GTAATGACTACTATG | 1130 |
rs147899661 | snp | C/G | 0.000412388 | 0.0143535 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730931 | AGGTAAGAGAGTGGT[C/G]GTTTGACAACATCTG | 1130 |
rs147918254 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | LYST | GRCh38.p7 | 1:235702725 | GGTTTTGCTGCACTC[A/G]ATTGAAATCCAAATG | 1130 |
rs147919836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804354 | CATCCCATCACATAT[C/G]CATCACGAGGAGATA | 1130 |
rs147926799 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235857094 | GGGATTACAGGTGTG[C/T]GTCACCACACCTAGC | 1130 |
rs147936793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235851111 | CAATTGCAAAATTGT[A/G]GAACCAACCCAAATG | 1130 |
rs147958303 | in-del | -/A | 0.131038 | 0.219882 | intron-variant | LYST | GRCh38.p7 | 1:235743035 | GTATGTATGTATGTG[-/A]AAAAAAATAGTATAT | 1130 |
rs147963856 | snp | A/G | 8.24967e-05 | 0.00642196 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809253 | TGGTTTTTAAAAGCC[A/G]AAACCAGAAGACCTG | 1130 |
rs147968213 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235706757 | CATAGCATTTATCTT[C/T]TATTAGAATAATTAG | 1130 |
rs147999076 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860429 | TCGACAAATGTATAA[C/T]AACATGTAGCTACCA | 1130 |
rs148018560 | snp | A/C/T | 3.31286e-05 | 0.00406982 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741558 | CTCCCAAGCTGCATT[A/C/T]GGAAGGTCTCCTTAC | 1130 |
rs148035743 | snp | A/T | 0.00335096 | 0.0407953 | intron-variant | LYST | GRCh38.p7 | 1:235812936 | TCTATGAAATTTTGA[A/T]AACACAAGTGATATG | 1130 |
rs148039222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235710107 | ATGACCTTTTAAAAG[C/G]TGATTAAGTTCCATG | 1130 |
rs148056887 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | LYST | GRCh38.p7 | 1:235680825 | GCTGGTCTCGAACTC[C/G]TGACCTCAGGTGATC | 1130 |
rs148076658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700971 | AACAAAGAAGGGGAA[A/G]GGATCTGAGGATGAC | 1130 |
rs148078167 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235709075 | AATACAGATTGTTTT[-/A]AAAAGAGTCACTTAC | 1130 |
rs148093422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756286 | CTAAAAAAGCTTTCT[A/G]AGTTTACAGCATAAC | 1130 |
rs148101450 | in-del | -/TTT | | | intron-variant | LYST | GRCh38.p7 | 1:235695648 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTTGC | 1130 |
rs148129352 | snp | C/G | 0.00011568 | 0.0076044 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235803004 | TACAACACTGAGAAT[C/G]CTCAGCTTCTTCTGA | 1130 |
rs148137941 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235793379 | ACATGAAATTGCCTA[C/T]ACCAACTGTCACATC | 1130 |
rs148141186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839947 | GTAGAGATACTGCCT[A/G]TTATCACCTTGTAAC | 1130 |
rs148159075 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235870057 | AAACTAGGCAAGAGG[G/T]GCCTCTGCCCTGGAC | 1130 |
rs148191682 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235830933 | TAATAGCTAAAGTTA[C/G]GCCACTTCACTTCTT | 1130 |
rs148228334 | snp | A/G | 0.039522 | 0.134904 | intron-variant | LYST | GRCh38.p7 | 1:235780331 | ATCATTTGAGCCCAG[A/G]AGTTCAAGGCTGCGG | 1130 |
rs148231834 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235690994 | CAATCTTGGCTCACT[A/G]CAAGCTCCGCCTCCC | 1130 |
rs148284819 | snp | C/T | 1.65168e-05 | 0.00287369 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235782018 | GCCAATCATGCAAAA[C/T]GTTTTATTGCTATCA | 1130 |
rs148295905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235749086 | TCATTACCTAATTGA[C/T]AGACATGACAGAAAT | 1130 |
rs148299757 | snp | C/T | 0.000594118 | 0.0172252 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805825 | AGGGCTTCCAAAAGT[C/T]GTATACTTTGAAGTG | 1130 |
rs148320083 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770259 | ATCTGCTCTGATGAG[A/G]ACTTCTAGAGCTGCT | 1130 |
rs148336486 | snp | C/G | 1.65165e-05 | 0.00287367 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809598 | AGAATCTGAAGAACT[C/G]CTTCCAAAAGCTCAG | 1130 |
rs148349802 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235836559 | TAAATGTATGCTGGA[G/T]GTACGGGATATTGAG | 1130 |
rs148371004 | snp | C/T | 0.000362695 | 0.0134617 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759465 | TATTTTGTAACCTGT[C/T]GATACTACAACCCAA | 1130 |
rs148389013 | snp | A/C | 0.000181481 | 0.00952404 | missense | LYST | GRCh38.p7 | 1:235693382 | TTTGAATAAAGTTTA[A/C]TGGAGGCTCACTTTG | 1130 |
rs148401720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702155 | TGTTTTTATAACGAA[G/T]AATTGAGTTGAAGAT | 1130 |
rs148409007 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235717657 | AACAGCAAGATTTGC[C/T]TACATTTCAGTGAGT | 1130 |
rs148409403 | snp | C/T | 0.00130057 | 0.0254675 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702886 | ATGTGGAACAGCTGA[C/T]GGGGAGTCTGCCCGT | 1130 |
rs148413735 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235849901 | CAAATGGAAACATAT[C/G]CCATGCTCATGGATG | 1130 |
rs148445520 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235674656 | CTGAACAATTAGGTC[C/T]TACCAGTCAGATGGC | 1130 |
rs148449089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795294 | CTTCTCTAAATAAAC[A/G]AAATGGTCAGGTGTA | 1130 |
rs148465680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235841627 | GGCAAGAGAACGAAT[A/G]AATGAAGGACAAAAT | 1130 |
rs148501897 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235832429 | AGATATAAAAGTTAA[C/T]GCCATATCAGTAAAA | 1130 |
rs148524904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783211 | ACTTTGTGTATATTT[A/G]TTTTAAAAGTTTTGC | 1130 |
rs148542548 | snp | C/T | 0.000115501 | 0.0075985 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800976 | TTTACTAGCAGAAAG[C/T]AAATTTAATTCCAGC | 1130 |
rs148595284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776979 | GAGTGTAGCTTTTTC[A/G]TGTGGTCCAAAAGAA | 1130 |
rs148611185 | snp | A/C/T | 0.000331953 | 0.0128791 | synonymous-codon, missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753109 | TAGACCATTATCCAG[A/C/T]AACATATCTGCTACC | 1130 |
rs148614675 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809030 | CAATTTAAAAGCATG[C/G]AGCAAAGGAATGATT | 1130 |
rs148617102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235682593 | TAAGATCATCCTCAC[A/G]TCTGTTTTATGCTTA | 1130 |
rs148646943 | snp | A/G | 3.29658e-05 | 0.00405978 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810157 | CTCTGGAATTTTCCA[A/G]AGCCATAGCATCTGG | 1130 |
rs148659211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838149 | TGCTTCTATTTTCTT[A/G]GTGCAATAAACAGCA | 1130 |
rs148662988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746005 | TTATACTACAGTTCT[A/G]CAAGATTCATGGGGG | 1130 |
rs148668054 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235678289 | GAAACCCTGTCTCTG[C/G]TAAAATTTCCAAAAT | 1130 |
rs148704397 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755499 | TCAAGGCCAATATGT[C/T]GACCAAAGAACATTT | 1130 |
rs148716608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789029 | TAACTCCAAAAAAGC[A/G]CGAGGGATGAAAAAT | 1130 |
rs148731121 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235864855 | GATCACCTGAGCCTG[C/G]GAAGTCGAGGCTGCA | 1130 |
rs148753672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235730436 | TATTGCTGCTTGATG[A/G]TACCACCAGCAGCTC | 1130 |
rs148780925 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235815827 | CACATTCATGAATAG[A/G]AAGAAACAATATTGT | 1130 |
rs148788623 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830315 | CCATGTGCGTCTCCT[C/T]CTCTTCTTCCTCCCT | 1130 |
rs148806269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235722298 | TGAAAGTGATTGAAG[A/G]ATTCTGAGCAGAGAA | 1130 |
rs148820427 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235835319 | CTAAAGATGGTATTA[C/T]ATTAGCTGCTCTGAC | 1130 |
rs148843615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785982 | TATTTCTAGCACTCT[A/G]TCTGAATCTATCACC | 1130 |
rs148859722 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235666109 | AATATGCCAAAGACC[A/G]CCAAATACCACAGAT | 1130 |
rs148873438 | in-del | -/AAACCCC | | | intron-variant | LYST | GRCh38.p7 | 1:235745488 | GGAAATGTAAAACTA[-/AAACCCC]CAGCCACTCTGGAAA | 1130 |
rs148891439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872535 | GCATTCCTTCTTCCC[A/G]GATACAGGGCAGGAT | 1130 |
rs148895243 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYST | GRCh38.p7 | 1:235778635 | CTCGTGATCTGCCCG[C/T]CTCAGCCTCCCAAAG | 1130 |
rs148908773 | in-del | -/AAG | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235669004 | ACTTCTCCTGAACAC[-/AAG]AATAGATGAATGTTT | 1130 |
rs148911572 | in-del | -/TAA | | | intron-variant | LYST | GRCh38.p7 | 1:235689008 | AATAATAATAATAAT[-/TAA]AATAATAATAATAAT | 1130 |
rs148929238 | snp | A/G | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775068 | CTTGAGTTTCTTCAC[A/G]GCTACTGAGTTCAAC | 1130 |
rs148930165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685288 | CTGGCTCCTTAACCT[A/G]CCCTTCTTTGCTTCC | 1130 |
rs148939514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235773366 | AAAAACGAGTATATG[C/T]TTCTATTCACGGTAG | 1130 |
rs148941493 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235812003 | AGGAATTAAAATACA[A/G]TAATTTTTTTTTTAA | 1130 |
rs148976681 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235748573 | ACCATTTAGGTAAAA[G/T]TACATATAAAGATAT | 1130 |
rs148980759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706911 | TACTTTTGGGGAATG[A/G]ACTACTGGCCTAAAT | 1130 |
rs149011086 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235839739 | TGAACCTGGGAGAGA[A/G]GGTTGCAGTGAACTG | 1130 |
rs149030004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235670748 | CAATTAAGTGCAAAG[C/T]GAGTGTGGAGTAAAG | 1130 |
rs149033064 | snp | A/C/G | 6.61294e-05 | 0.00574988 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759060 | TGTTTCTATCAACAA[A/C/G]ACTTGGCCAACGGCC | 1130 |
rs149047210 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235830503 | TATGTGTTTTTGTTG[C/T]TTGTTTCTAACTGAA | 1130 |
rs149049312 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868536 | TTTCTGTTAACCTTG[A/G]GTAGAAAATAATAGA | 1130 |
rs149051112 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734535 | GCACTGGGAGGGATG[A/C]ACTTGTGACCACATA | 1130 |
rs149087734 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235690845 | AGAAGGCTGTCCATA[C/T]GATTTACAGTCTGGA | 1130 |
rs149098802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826757 | ACGACCATGGCTCAC[C/T]GCAGCCTTGATTTCC | 1130 |
rs149137664 | in-del | -/TGTGTG | | | intron-variant | LYST | GRCh38.p7 | 1:235805539 | CTGACACTTATAAAA[-/TGTGTG]TGTGTGTGTGTGTAT | 1130 |
rs149138177 | in-del | -/AAAAG | | | intron-variant | LYST | GRCh38.p7 | 1:235755389 | GCGAGACTCCGTCTC[-/AAAAG]AAAAGAAAAGAAAAG | 1130 |
rs149140829 | snp | C/T | 3.30721e-05 | 0.00406632 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716714 | AAACAAAAGCTACCT[C/T]GTATGTGTCCACATA | 1130 |
rs149168374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805481 | AGTATCACACAAAAA[C/T]TTAGATCTTTCAACT | 1130 |
rs149188765 | snp | A/C | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759460 | TGCAATATTTTGTAA[A/C]CTGTCGATACTACAA | 1130 |
rs149190784 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235675593 | GCCAGAACATGGTGC[A/G]CCCTAACTCCACAAC | 1130 |
rs149193899 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235713998 | TACATTAAATGAAAT[A/G]TAGTCTTGGATGGAG | 1130 |
rs149209695 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662237 | TAAGTAAAATTTTTA[C/T]GAAGAAACAGAATGT | 1130 |
rs149211580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235743542 | GATAAATGAACCCTG[A/G]CACTTATCAGTATTC | 1130 |
rs149241083 | snp | C/G | 3.29462e-05 | 0.00405857 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702765 | ATAGGTGATTTCTTT[C/G]ACCTGTTCTCGGGTC | 1130 |
rs149255066 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235686316 | AGGTTGCAGTGAGCT[C/G]AGATTGTGCCATTGC | 1130 |
rs149258083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776387 | GAAAACTTGATAATG[G/T]TGCAAAAGTTATACT | 1130 |
rs149292888 | snp | C/T | 6.64993e-05 | 0.00576587 | missense | LYST | GRCh38.p7 | 1:235664493 | TTTCTAATCCCCCAG[C/T]GATTACATTGATAGA | 1130 |
rs149293037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710010 | TTAAAAAAATTATCC[C/T]AAAGGAAATGTTACC | 1130 |
rs149305367 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235859473 | AAAATTGTTTTATTG[G/T]GTTTAGGCTTCTCTC | 1130 |
rs149309260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235770452 | TGTTAAAATTTATTC[C/T]CTATTATTTTTTGTT | 1130 |
rs149324134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841267 | GCAGGATTAGAAAAG[A/G]AAAACAGAAAATAGA | 1130 |
rs149344884 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235673677 | CTAGGAGAAAATGCC[A/G]TTAGAAAGGACTCTA | 1130 |
rs149374093 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235832076 | TTCAAAGCTACTAAC[A/G]TCATTCTATAAATTT | 1130 |
rs149420572 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828654 | ATTTTATTAGAGTCA[C/T]TCCTCGATATTTACT | 1130 |
rs149467186 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854924 | GAATGACAAATGTCA[C/T]TCCAATTCATAGGGA | 1130 |
rs149469753 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235721720 | TAAATCTGAAGTTTG[C/T]CAATTGTTAGCGCTA | 1130 |
rs149470152 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810129 | GTGTTTGACCCCTGT[C/T]TTGGAATAATCTCTC | 1130 |
rs149520131 | snp | C/T | 3.29875e-05 | 0.00406112 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809144 | CTGCTGTAGTAAGCG[C/T]AAGCACTGATGGGCA | 1130 |
rs149521672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716052 | TTCCACAGCAATGAC[A/G]CATTTTCAACTGCTG | 1130 |
rs149523135 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235819121 | TGGCCCCTCTGCTGG[A/G]ATTGTAGTCCTGAAG | 1130 |
rs149529363 | in-del | -/GT | | | intron-variant | LYST | GRCh38.p7 | 1:235750531 | AATACTCTGGAGATG[-/GT]GTGTGTGTGTGCATG | 1130 |
rs149542245 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235800629 | AAAAATATTACCCAG[C/T]CTCAGAAATAGATGA | 1130 |
rs149557229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235703726 | ACTCCATTCTCCTCA[C/T]CACAACTCCCAGCAC | 1130 |
rs149558986 | snp | C/T | 0.000164908 | 0.00907891 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806310 | CTCGAGAGATATACA[C/T]GGCAGCATATGACTT | 1130 |
rs149578375 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235788222 | TGGAGTGCAGTGGCG[C/T]GATCTGGGATCACTA | 1130 |
rs149579373 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235667942 | GCAGGGATTACAGGC[A/G]TAGCCACCGTGCCTG | 1130 |
rs149581246 | in-del | -/AAT | | | intron-variant | LYST | GRCh38.p7 | 1:235689047 | AACAACAACAACAAC[-/AAT]AATAATATCCTAGCT | 1130 |
rs149629549 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235782857 | TTCAAAATTTCTGTC[C/T]AGCCATTGAAATGCC | 1130 |
rs149637949 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235874939 | GTGTTCCAAGCCCAG[A/G]CTCCTCCTCCAACCA | 1130 |
rs149689763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235740877 | ATTTTTTAAGAAACT[A/G]TTAAACAGCCCTCCA | 1130 |
rs149692312 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235835007 | GCAACAACCTCTGCC[A/G]CCTGGGTTCAAGTGA | 1130 |
rs149693430 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235849642 | CCTCTAGAAAGCTCA[C/T]GGAACTGATAAAAGA | 1130 |
rs149698234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758234 | GATATCTCATCACCA[A/G]AGCAAGGTCATCTGT | 1130 |
rs149733805 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698837 | GAGATCACGCCACTG[C/T]ACTTCAGTCTGGGCA | 1130 |
rs149744238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829778 | AGATGTATACAAGCT[A/G]AAGGACTCAGTAATT | 1130 |
rs149762259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826323 | ATCCAAGGACTTTTA[C/T]AGGAATGTTCAAAGC | 1130 |
rs149803155 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235684461 | AATCGATTTGTAGGG[C/G]AAGTCAGAAAGGGGA | 1130 |
rs149834532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235821398 | GCTGAGATTGTGCCA[A/G]TGCCCTCCAGCCTGC | 1130 |
rs149853134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803985 | CATAATTTTAGGAAA[C/G]AAAATTACAACAGTT | 1130 |
rs149855689 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235679724 | AAACCAGGGAATTCC[A/C]GGGTTCTCCCATGCA | 1130 |
rs149858197 | snp | C/G | 0.102014 | 0.201495 | intron-variant | LYST | GRCh38.p7 | 1:235764720 | GTTGGTCAGGCAGGT[C/G]TTGAACTCCTGACCT | 1130 |
rs149893177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235670137 | TTGTTCTGTAAACTA[C/T]CTTTCCCACCTTAGC | 1130 |
rs149903470 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791156 | GGTGTGATTGCTGGC[A/C/G]CCTGAATCCCAGCTA | 1130 |
rs149908107 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235706075 | TGGGATTACAGGCAT[C/G]AGCCACCATGCCTGG | 1130 |
rs149940116 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235732848 | ACAATAAAAATAACT[A/T]TATTTGCTGAAAATA | 1130 |
rs149945984 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235744885 | GTGACAGAGTGAGAA[A/C]CCATCTCAAAAAAAA | 1130 |
rs149951019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235878273 | CAAGTTGCATTCCCA[C/T]CCTGAGTGATGAGGG | 1130 |
rs149991106 | snp | C/T | 3.31439e-05 | 0.00407073 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781954 | GCAAATTTCCCAGGT[C/T]CCATTTTCCAGCCAA | 1130 |
rs149992238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235778392 | ATTTATTTATTTTTC[C/T]GAGACGGAGTCTTGC | 1130 |
rs150026506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864660 | CCTGGGGCCGAGCGC[A/C]GTGGCTCACGCCTAC | 1130 |
rs150030873 | snp | C/T | 0.000164987 | 0.00908108 | missense | LYST | GRCh38.p7 | 1:235677598 | AGAGATGTATTTGAG[C/T]CTCCATTTCTATTTC | 1130 |
rs150043337 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235772442 | AAATCATCAGTACCT[A/G]CTAGAACCCTGCCAC | 1130 |
rs150047771 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733688 | ATCCAGACGCTGAAA[A/G]AGACTAAACAAATAA | 1130 |
rs150064168 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | LYST | GRCh38.p7 | 1:235844280 | AGAAAAAAAGATAAC[A/G]CCATTTATATCATTT | 1130 |
rs150065814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712826 | TTTTTTTTCCAGGGT[A/G]GACTATTAATAATAA | 1130 |
rs150078571 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235727366 | TGACCTCAGGTGATC[C/T]ACTCACCTCAGCTTC | 1130 |
rs150080858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828362 | GTGGTGACAGATGCA[C/T]TTACCTGTGACTACA | 1130 |
rs150132367 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235823640 | CAAAAGCAAAGCAAA[A/G]TTCAGCCTTCGCTGT | 1130 |
rs150147284 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | LYST | GRCh38.p7 | 1:235693043 | AAAGTTGGCCAGGTG[C/T]GGTGGCTCACACCTG | 1130 |
rs150173139 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235681393 | AGAGCACGGGGCCTG[A/G]TGTGTGATGCCTAGC | 1130 |
rs150185548 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235858108 | ATTGATTCCAACACA[C/G]AAGACTTAATGCTCT | 1130 |
rs150208537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672294 | CCATGACTTTGGATA[A/C]GATCACCTAGTACAG | 1130 |
rs150221594 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | LYST | GRCh38.p7 | 1:235810817 | TAAACACTAGCTGAC[A/G]TTACTTCAAAGGATA | 1130 |
rs150222948 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | LYST | GRCh38.p7 | 1:235697177 | AGAGCCAAATCTTTC[C/T]CCGTGGGGCTGGCTG | 1130 |
rs150225147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235708353 | TGCCATTTTAAAGTA[A/G]AACATGTATGTAGGA | 1130 |
rs150259778 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235666299 | GTAAAAAGGAATGAA[A/G]CATGCGAAAACATGG | 1130 |
rs150268472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235881633 | TCACTGTGTGTGTGT[A/G]TATATATTTACATAC | 1130 |
rs150270086 | snp | C/G | 0.000181394 | 0.00952177 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759171 | ATCCCTTTAGGTAAT[C/G]AGGTCGGCGTGGGCA | 1130 |
rs150288597 | snp | A/G | 0.00350407 | 0.0417104 | intron-variant | LYST | GRCh38.p7 | 1:235782106 | CATTAAAAACAAAAC[A/G]AAGTTAAAGCAATGA | 1130 |
rs150304907 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661665 | AGTACTGTAAACACC[A/G]TATGAATTAAATTTC | 1130 |
rs150306354 | snp | A/G | 0.00554856 | 0.052379 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746438 | CTTGGCTCATTCTCC[A/G]TTGCATCATCACATG | 1130 |
rs150321124 | snp | C/T | 0.00042888 | 0.0146375 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805928 | CATTTATGGAAGAAA[C/T]ATGCTGTAACTCTAA | 1130 |
rs150358286 | snp | A/G | 8.24396e-05 | 0.00641973 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734626 | GGTGATTATGTATCA[A/G]CTCTGACAAATACAA | 1130 |
rs150376455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235715806 | AGAAATGTAAAAACT[A/G]TGTCACATTATTGGT | 1130 |
rs150424923 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837277 | TGAGTGGTATCTCCC[A/G]GAAACCAGGTGAAGA | 1130 |
rs150427167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235703622 | ATATTTAATCAGTCA[C/T]AGTGGCTTTCATTAC | 1130 |
rs150430766 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235760581 | ATGGGCATCAATACC[A/T]CCTGTGGGATTGTTG | 1130 |
rs150431096 | snp | C/T | 1.65776e-05 | 0.00287898 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773860 | TGCTTTACTCCATAT[C/T]TTCCAGTCAAGCAAT | 1130 |
rs150480190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700004 | AGGATTCCCTATTTA[A/G]TAAGTGGTGCTGGGA | 1130 |
rs150482417 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235797816 | TGCATCAAAGGATAC[C/T]ATCAACAAGTAAAAA | 1130 |
rs150482928 | snp | C/T | 9.89006e-05 | 0.00703139 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806233 | AACATGTAGATCCAA[C/T]GACACATAGACCAAA | 1130 |
rs150488664 | snp | A/G | 4.94964e-05 | 0.00497451 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715209 | TTCTTACCTTGATAG[A/G]CTAAAAACATTTTAG | 1130 |
rs150500390 | snp | A/G | 1.68417e-05 | 0.00290182 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813004 | GGACAGGTATCTTCC[A/G]TACCAGTGGAAGGAG | 1130 |
rs150530757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235757949 | GCATGTCAGAAAAAC[C/T]CAGTTCACTCACAGA | 1130 |
rs150534643 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235674744 | CATGATTGGAGTCCA[A/G]TGTTGTACTTTTATC | 1130 |
rs150547250 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235813582 | ACTGCATACTATGTC[C/T]ACAAAAATACTGTCT | 1130 |
rs150582714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750513 | ATTTCAAACAATTTA[C/T]CAAATACTCTGGAGA | 1130 |
rs150585616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840993 | CCTGCGAAGAACACA[C/T]AAGAAGAACTGAGGC | 1130 |
rs150587151 | snp | C/T | 4.94376e-05 | 0.00497156 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759364 | ACAGCTACTGATGAA[C/T]GCGTCCTCTTTGCCT | 1130 |
rs150603201 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235783482 | CCGGGGCCTGTCGGC[A/G]GGTGTTGGGGCAAGG | 1130 |
rs150623574 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LYST | GRCh38.p7 | 1:235665052 | GCCCACCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 1130 |
rs150636017 | snp | C/G | 0.00100619 | 0.0224078 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806053 | GTTCTCTTAGGTTGA[C/G]AAATTCTGTTTAAAT | 1130 |
rs150656433 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235870635 | TCTCTTTCATAGCAC[C/T]CATCAGCTTCTAACA | 1130 |
rs150658860 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235736569 | GCAGGCTGGAGAGTT[A/C]ATCAGAATCAAGTTG | 1130 |
rs150672439 | in-del | -/CTCA | | | intron-variant | LYST | GRCh38.p7 | 1:235832595 | CATTTCACATGAGCT[-/CTCA]CTCTTTAATAGCTGT | 1130 |
rs150687112 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235679139 | CTGTTTAGCTAGGGC[A/G]TGTGACCTTCACCTG | 1130 |
rs150727233 | snp | A/C | 1.99043e-05 | 0.00315464 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235782084 | CAAAGTAACATCAGG[A/C]TTCCTACATTAAAAA | 1130 |
rs150738700 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705730 | AAGAATAACTGAAAA[G/T]ATGGTTCAGGATTAT | 1130 |
rs150742196 | in-del | -/TA | 0.350109 | 0.229081 | intron-variant | LYST | GRCh38.p7 | 1:235742570 | TGGTAAATTTTATGT[-/TA]TATATATATATATAT | 1130 |
rs150755214 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235763407 | GGAGCTACCCTTGAC[A/C]ACTACCTTTCCTTTA | 1130 |
rs150757949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854180 | ACACATCAGGCACTA[C/T]TGTAAGCACTCTAGG | 1130 |
rs150793346 | snp | A/G | 0.000324517 | 0.0127339 | intron-variant | LYST | GRCh38.p7 | 1:235800407 | GATTAAAAAAAATAC[A/G]AAATTAAATTACTTA | 1130 |
rs150813257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829523 | GATTGTAGAGTTTTA[C/T]GATCACAAAATAATT | 1130 |
rs150814737 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | LYST | GRCh38.p7 | 1:235698325 | AAAAGGCATCACTGA[C/T]GTATAGACTATCTTT | 1130 |
rs150826004 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884353 | GGTCTCGATCTCCTG[A/G]CCTCGTGATCCGCCC | 1130 |
rs150849914 | snp | C/G | 0.000428308 | 0.0146277 | synonymous-codon | LYST | GRCh38.p7 | 1:235662991 | CATTGGCTGTTTCAA[C/G]CGCTGCTGGTCCTTC | 1130 |
rs150865625 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235825078 | ATCAAGATAACTTAC[C/T]TACATTACAGAATAA | 1130 |
rs150868699 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235693540 | TGCTCGACTGTTACA[C/T]GACAGCCCAAAACTG | 1130 |
rs150906747 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235683669 | TTTGGCCACATCCTA[C/T]GTGGCACTTGGTTGG | 1130 |
rs150916533 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235772097 | AAGCATGGTGGTGCA[C/T]ACATGTAGTCCTAGC | 1130 |
rs150925628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235880457 | AGTGTCATCATTTGA[C/T]ACCGTCATAACAGTG | 1130 |
rs150936115 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802749 | CATTGTTGCATATAT[A/G]AATGCCAGACTGTTG | 1130 |
rs150953050 | snp | C/T | 0.000759778 | 0.0194759 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806173 | AACTTATGGCATACT[C/T]GGAAACCACCAAGCC | 1130 |
rs150968361 | snp | A/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809302 | GCATAAAATGAGAAT[A/T]TTCACATCGTCTGTG | 1130 |
rs150970967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740441 | CGTCCCCCTTCCACA[C/G]AGACAACTACTGTCC | 1130 |
rs150974382 | snp | G/T | 3.38312e-05 | 0.00411272 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744156 | AATGTCTGAATTAAA[G/T]TCTTTGAATTGAAAA | 1130 |
rs150974735 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661195 | AATAAATAATCCCCC[A/C]AAATTAATTTTTATT | 1130 |
rs150982210 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235873172 | GGTATTGTGTTGAGT[C/T]CTGACATAAACATCA | 1130 |
rs151018553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235823596 | GCCTCTGCCCTTCAG[A/G]TCTCCCCATTAGCCA | 1130 |
rs151022866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719769 | GGGAACAAACCAAAC[A/G]ACGTCATGGGAAGCA | 1130 |
rs151059404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235707750 | GCAAACAAATCCTAA[C/T]TAAATATCCAACAAT | 1130 |
rs151071827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857806 | ATATAAAATTTCACA[A/G]GCCAAGAGAGAAGAG | 1130 |
rs151074605 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235722767 | GGGATTACAGGCATG[A/C]GCCACTGTGCCCGGC | 1130 |
rs151124536 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235850209 | CACAATAGAGAACCC[A/T]GAAATAAACCCAAAT | 1130 |
rs151130915 | snp | C/T | 0.000362946 | 0.0134663 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805919 | CTTCTTCCACATTTA[C/T]GGAAGAAATATGCTG | 1130 |
rs151147069 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235753778 | AAAATATGTGGTGAT[A/G]TATGTCCTCTTTTCT | 1130 |
rs151148773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843980 | TGGAAAGACTTTTTT[C/T]CAAAAATGTTATGTG | 1130 |
rs151167023 | snp | C/T | 4.94817e-05 | 0.00497377 | missense | LYST | GRCh38.p7 | 1:235677582 | TCTTCTGTGTGACCA[C/T]AGAGATGTATTTGAG | 1130 |
rs151183836 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | LYST | GRCh38.p7 | 1:235790008 | TAAAAGGTATGATAT[C/T]GCAGCAAAATATTCT | 1130 |
rs151187564 | snp | G/T | 1.65745e-05 | 0.00287871 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802918 | TTTACCATCATCCTG[G/T]GTTTCGCCATCTTCA | 1130 |
rs151188898 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235694890 | CTATTAGGACAGTAT[A/T]TCTTAAATAGGATCT | 1130 |
rs151200400 | snp | A/C/G | 0.00597694 | 0.0544006 | intron-variant | LYST | GRCh38.p7 | 1:235838177 | GCAAGACTGCCAGCT[A/C/G]AGAGTGAGAAGTGGG | 1130 |
rs151209766 | in-del | -/TA | 0.41325 | 0.18934 | intron-variant | LYST | GRCh38.p7 | 1:235851188 | ATGTATATGTGTGTG[-/TA]TATATATATATATAT | 1130 |
rs151228697 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235774193 | CTTACAAATATTTTT[A/C]AGTGAGTACTCAGGT | 1130 |
rs151236654 | snp | A/G | 3.30316e-05 | 0.00406383 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830347 | GCCTCCACCCTCTGG[A/G]CCACTGCATTGCAAA | 1130 |
rs151240866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235730481 | GATAGAGATGTTAAA[C/T]AGTCAATTACAAAAT | 1130 |
rs151256487 | in-del | -/GTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235875501 | CTGGTGGAGAGTCTG[-/GTTT]TTTTAATAAGGACCA | 1130 |
rs151270469 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235675678 | CTGTGCCTCTTCAGC[C/T]GCTGTTCATTTCTAT | 1130 |
rs151281961 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235816020 | CTGTATTCCTAGCCA[C/G]TCAGGAGGTTGAGGC | 1130 |
rs151304763 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235760418 | CACTTCTTGCTGTTA[C/T]TAGTGAGAATAGTTT | 1130 |
rs151337641 | snp | A/G | 7.24795e-05 | 0.00601951 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781046 | GCCTCTTGTGAACCA[A/G]CCTTAGCTCCTGAAT | 1130 |
rs180680228 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235754746 | GTGACCAAAAGATTT[C/T]GTTAAGAGTGAGTTC | 1130 |
rs180684417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803220 | ATTATGAAATTCACT[C/T]AGCAAAATTTCCCAG | 1130 |
rs180688851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235765136 | TTCTTCATGCTGTAA[C/T]CCTCATTCCCAATTG | 1130 |
rs180690227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784110 | GTCTTGAATTCCCGT[A/G]CTCAAGCAATCCTTC | 1130 |
rs180697255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820069 | TTTTTCCATTCAAGA[A/C]ACATATTTCAAGTAC | 1130 |
rs180705761 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235775744 | GGGTGGCTAAGGCAG[G/T]GCACAGCCAGGGGAA | 1130 |
rs180714426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691214 | TGAGCCACCGCGCCT[A/G]GCTACAGTTTACAAG | 1130 |
rs180716195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813453 | ATGTGAAGCCTTCAT[A/G]CAGTTAAATGAAAAA | 1130 |
rs180722169 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235839104 | TGTTGGGATTACAGG[A/C]GTGAGCCACTGCACC | 1130 |
rs180726927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795257 | GTTCAGTATTCACTT[G/T]TAGGTCCCAAACCTG | 1130 |
rs180734733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673676 | TCTAGGAGAAAATGC[C/T]GTTAGAAAGGACTCT | 1130 |
rs180735002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723821 | AAGTTTAAATTACTC[C/T]TTTCAGTCATTTTGG | 1130 |
rs180736462 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235742369 | GTGAGGTAGGAGAAT[C/T]GCTTGAACCTGGGAG | 1130 |
rs180740501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705448 | TGGAATGCAGTGGCA[C/T]GATCATGGCTCACTG | 1130 |
rs180870264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235869695 | GTGACTAAATGGATA[C/T]ATAAATCAAATCATG | 1130 |
rs180889778 | snp | C/G | 0.000198151 | 0.00995168 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806489 | TCTTCCGTCTCTTTG[C/G]ATAAGCTTCTTTGAG | 1130 |
rs180910802 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235842502 | AAAATGAAAGCCCTA[C/T]AATGACAGAGATTTT | 1130 |
rs180911013 | snp | A/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759087 | GGCCAACAGCTGCAG[A/T]TCCGTTCTGTGAAGG | 1130 |
rs180915946 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235779157 | CAGGCATGAGCCACC[A/G]TGCCTGGCCGAGGGT | 1130 |
rs180916190 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235824159 | GATTTTTAAAAACCT[A/C]TTATAATGTTTGAAT | 1130 |
rs180923219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799370 | TACTTATTAATTATA[A/T]AGGGAAAATAGTAAC | 1130 |
rs180925104 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235860310 | CAGCCCCCCTAAACT[C/G]GTACATTTGTTATAA | 1130 |
rs180926642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878976 | GGCTGTTAGAGTACC[C/T]ATCACCTGAATAGTG | 1130 |
rs180935953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688678 | AGTGAAATCTCAGAG[C/T]GTGAGTCTTTATATA | 1130 |
rs180961787 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235719496 | ATAATCATCAATGGA[G/T]GAAACCATTAGGTAC | 1130 |
rs180962117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235834115 | TTAGACAATACCAAA[A/G]CCAAACATTAATTTA | 1130 |
rs180964954 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739024 | ATTTCACTGTCTAGG[A/C]TACAATAGGATTTTA | 1130 |
rs180969423 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235701999 | TCTTAAAATAGGTCA[C/T]AGATTACTGCACTTT | 1130 |
rs180970691 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235787825 | GTTTGTAACGTTTAC[A/G]AAGTATATATTCCTA | 1130 |
rs180976309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729219 | AATATAAATTATGGA[A/C]AATCTTAAAATAGAC | 1130 |
rs180984786 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235694805 | TCCATAAACCAAGGT[G/T]TCTCATTCCAGTACC | 1130 |
rs180986999 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817716 | GGGCCTCTTTCAGGA[C/T]GGAGGGTGGGAGAAG | 1130 |
rs180992512 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235850882 | AAAAAACAGTAGATG[C/T]TGGCATGGACGTGGT | 1130 |
rs180994534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235770850 | AAGAGTAGTTAGCAT[C/T]CCTTGACAGTGCCTT | 1130 |
rs181001400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235708607 | GCAGAGGGTGCCTAC[A/G]TTGCCAATCTCAATA | 1130 |
rs181033914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235748211 | ACTGTGTGTATGTGC[A/G]AGTGCATGGCAATTT | 1130 |
rs181067209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678626 | GAGCTATATACTGAC[C/T]ACCCAGTTAAACAAA | 1130 |
rs181145009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235880267 | TATTAGTTTAGCAAT[A/G]TATGTGAAAAAAACT | 1130 |
rs181186224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850632 | ACAATCTATACATCT[C/G]ACAAAGGACTAATAT | 1130 |
rs181191579 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809280 | CCTGAGAGATCTCGG[C/T]GATGATGCATAAAAT | 1130 |
rs181196356 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235844426 | CTGAGGCCTACAGGT[C/T]CAAGGTCACAGAAAT | 1130 |
rs181197140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235817098 | AAGAAGACATACATG[C/T]GCCAACAAGCATATG | 1130 |
rs181198974 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235869425 | TGCAGTGAGCTGAGA[G/T]AGCGCCACTACAGTC | 1130 |
rs181200889 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826499 | TGAATTTCAGAGACA[A/T]GAGAGTACATACTAC | 1130 |
rs181205574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694304 | ACAGGCTTGAGCCAC[C/T]GTGCCCAGCCCTCTC | 1130 |
rs181206683 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235833648 | TAGATGAAACAAATA[G/T]TCTTAGAACAAAGCT | 1130 |
rs181230360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687905 | TTTCTTACAGTTTCA[A/G]GCTGTCTCTTGCTGG | 1130 |
rs181233640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668952 | AGACTAGCAAAAATT[A/C]TTTCATATCTGAAAT | 1130 |
rs181236846 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738823 | TGCACCCAATTTCCA[A/C]CATGATTGGTGGAAT | 1130 |
rs181239697 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235861620 | TTCTTAAAGTGTAGA[A/C]CTTAAATTCCAGAAG | 1130 |
rs181286323 | snp | A/G | 0.0011452 | 0.0239016 | intron-variant | LYST | GRCh38.p7 | 1:235677640 | ATTTTAAAATTAAGT[A/G]TGAGATAAAAACCAC | 1130 |
rs181303784 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235701644 | TCAATCAATCAATCA[A/G]TCAATCAAGTGACAG | 1130 |
rs181307048 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235718776 | GGAAAGGCAGAATAA[A/G]TGCTGAATTCTGTTC | 1130 |
rs181339105 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235758200 | CTGCGATAGCAGAAG[C/T]AGAGGAAAATATAAG | 1130 |
rs181365093 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235799169 | AGCTTTTCCTTACAG[C/T]ACAATCTCAGTTAAT | 1130 |
rs181393040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829540 | ATCACAAAATAATTA[C/T]TCATTTTCTACTAAA | 1130 |
rs181416487 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235848158 | TCTCAATAGATTTAA[A/G]AAAACTGAAATTATA | 1130 |
rs181422332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865519 | ATACATATATATAAT[C/T]ATATAGTTTGTGAAG | 1130 |
rs181426875 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235883728 | TGGCTCTTTGGCAGG[G/T]GGCCACGCTTGTATC | 1130 |
rs181427788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854942 | CAATTCATAGGGAAG[A/G]AGATCCCAACTGCTT | 1130 |
rs181442569 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235778149 | CATGGTCTTGTTATG[C/T]TGCCCAGGCTAGTCT | 1130 |
rs181450025 | snp | A/G | 0.000651351 | 0.0180347 | intron-variant | LYST | GRCh38.p7 | 1:235729670 | ACTCTGTCAAAACAT[A/G]TTTAAAATTACTATG | 1130 |
rs181450230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235816055 | GAATCACTTGAACCC[A/G]GGAGGAGGAAGATGC | 1130 |
rs181454463 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797962 | TCAAACATAAGCAGA[A/G]GGCTTGAATAGATAT | 1130 |
rs181491421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748653 | CAGAGCTTTGTTCAC[G/T]GGGCAGCAGGCAACT | 1130 |
rs181492419 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660804 | CTGAGGCTGGAGAAT[C/T]GCTTGAACCTGGGAG | 1130 |
rs181503042 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235824706 | TATGAACAAAATGGA[A/G]TTTATTCCAGGAATG | 1130 |
rs181504476 | snp | A/T | 0.000551098 | 0.0165905 | intron-variant | LYST | GRCh38.p7 | 1:235709055 | ATTCAGGTTCTATCT[A/T]ATATAAATACAGATT | 1130 |
rs181510711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757835 | AAAACATGTCCATCA[C/T]TGCAGAAAGTTTCAC | 1130 |
rs181517968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679101 | TTCCTTGTAACAACT[A/G]GCTTGAGCTGTGTAG | 1130 |
rs181519419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695156 | CCAATAAGCATTTAT[C/T]AAGCACTTAGAATGA | 1130 |
rs181519807 | snp | C/T | 0.000711714 | 0.0188507 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738551 | AGTTCACACATTAAG[C/T]TGTCATGGGTGAGTC | 1130 |
rs181524865 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235687224 | GTCAGATATAGTAAT[A/G]TTCCGTAACTTTGAG | 1130 |
rs181564495 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235873739 | GGTCTACAAATTTCT[A/G]ATTAACTTTCACCTG | 1130 |
rs181567909 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235875926 | GATTTAAATTAAAAT[A/G]TGCTTTTTCTTGGCC | 1130 |
rs181571082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717366 | CACAGTGTAGAGTAT[G/T]TATGCATGCGTACAA | 1130 |
rs181608200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235771310 | AAATATAATTAATTA[C/T]GTAAGAAAATCTTAT | 1130 |
rs181624063 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235807775 | AAAAGTAATTTTAAT[A/G]TTCTTATTTTTGTTT | 1130 |
rs181635489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235705222 | TTCAGAGTCTCTGCA[C/T]TTAATCGCCATACTT | 1130 |
rs181639307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795007 | CAGTGGGCATTGGGG[C/T]ACATCTAGTAAGAGA | 1130 |
rs181651837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235775407 | CTCTGCATTATGTGG[C/T]AAGGGAGATAAAAAG | 1130 |
rs181653909 | snp | C/T | 0.00640183 | 0.0562133 | intron-variant | LYST | GRCh38.p7 | 1:235813099 | CTTCATGTTCTAAGG[C/T]GATAAGACACATCAG | 1130 |
rs181660992 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235701298 | ATGGCATTTATTAAT[G/T]TTCAGGGATGTATTG | 1130 |
rs181663359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847321 | CTTTTTCAGACAAAC[A/G]CATGCTGAGAGAATT | 1130 |
rs181664954 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235829316 | CAGAAGTACTGTTTT[A/C]GTCTCCATATTTCCT | 1130 |
rs181665937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235668473 | TGACAAGGCCTTTTT[A/G]TTCAAATTGGAAAAA | 1130 |
rs181694082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691160 | CCTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC | 1130 |
rs181702989 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235753422 | ACCTGTTTTTAAAAT[G/T]ACAGAGTCCCTCCAA | 1130 |
rs181709895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673308 | CCAAAATATTACTTT[A/T]AATGCTTGTTTTGTT | 1130 |
rs181712461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235736069 | TTTTATTCATTGTGA[A/G]TATCAAAGGAAACAC | 1130 |
rs181807448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803468 | AGGATTTTTATAAAT[A/G]CCTTATAAGTTAGGT | 1130 |
rs181816357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235864551 | GGCAACAGTTCCGGA[C/T]TGGTATCCCAGCTTC | 1130 |
rs181820067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235821064 | ACTTTACCACTACAT[A/G]TATTTAAAACATAAT | 1130 |
rs181822268 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235856140 | AGTTTCTATCATACT[C/T]GGTAGTTTCTATCAC | 1130 |
rs181823978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235698822 | AGCTTGCAGTAAGCC[A/G]AGATCACGCCACTGC | 1130 |
rs181831794 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235874446 | AGCAGCGCGGAGGGA[A/C]ACCCAACTCCCATCC | 1130 |
rs181846686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235723232 | GTTTTGTACAGGTTA[C/T]GTTTGAGATGTCAAT | 1130 |
rs181867869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784788 | TACTTACAACTCCAG[A/C]CCCAGCTCCATCTGA | 1130 |
rs181881771 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883336 | TTAGATCCTGGCTTC[C/T]GTTCAGCTGACTTAG | 1130 |
rs181889305 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752309 | CAGTCATTCAGTATT[A/T]ATTCATGCTTATTCT | 1130 |
rs181893285 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665045 | GTGATCAGCCCACCT[C/T]GGCCTCCCAAAGTGC | 1130 |
rs181902010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735227 | AAAACTGAACTAGAA[A/G]GGAAAGCTTCCTTTA | 1130 |
rs181924270 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235663886 | TTCATGATGACTTCA[A/G]TTGCACATTTCTTTA | 1130 |
rs181954114 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235698223 | TACATAAAATAAAAA[C/T]AATATATTAAGCAAT | 1130 |
rs181957041 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235682314 | TGGGCAAAAGGGCAA[G/T]ACCCTGTATGCCCAA | 1130 |
rs181997163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846537 | AAATCCCTGATTTAC[C/T]TGACAAAGAATTCAG | 1130 |
rs182058224 | snp | A/G | 1.85414e-05 | 0.00304472 | intron-variant | LYST | GRCh38.p7 | 1:235774903 | AAGAATAAATTTTAT[A/G]AAGACATACCTTCAA | 1130 |
rs182070820 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706017 | AGGCTGGTCTTGAAC[A/T]CCTGACCTCAAATGA | 1130 |
rs182086270 | snp | A/C/T | 0.000381263 | 0.0138026 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741387 | TTGTATTTCACCAAA[A/C/T]GTTTTACTTCTCTTA | 1130 |
rs182093490 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682559 | CCTGGGGCTGGAACA[C/G]AATGCACAGCTCTTA | 1130 |
rs182097214 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235743064 | ATACAGGTTTCAGTA[A/C]CATCTGTGGTTTCAG | 1130 |
rs182100215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235706674 | CTCCCTTACATATTA[A/G]TATTATATGTAAAGT | 1130 |
rs182108237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683410 | TTCGTGACAGAATAA[A/C]CCGACAGCAACTATT | 1130 |
rs182113345 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235745049 | TTTTTTAGAATTCCA[C/T]TTTGACTTATCTATA | 1130 |
rs182117602 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235665248 | CCAAATATGAGTTAT[A/G]ATTGAAAATACTTGG | 1130 |
rs182120547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235767632 | AGTCACTGGTATTCT[A/G]TTTTATTATTTTTTT | 1130 |
rs182121637 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235812229 | ATCCTTTAGGCTGGG[C/T]ACGGTGGCTCATGCC | 1130 |
rs182122769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713908 | AATATATGAATACAT[C/T]CATAATAGTAACATG | 1130 |
rs182125090 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235726144 | TTCCTTTTAAAAAAA[C/T]TGCATTTACTTACTC | 1130 |
rs182160496 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235674121 | GCCCTCCAGAGCTAT[C/T]TGGCCTCCAAGTAAC | 1130 |
rs182294306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235669066 | AGGTATCTGTGGTAT[A/G]ATGAAAAATAAGTAT | 1130 |
rs182298482 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235802049 | AAATATAACAATTAG[C/T]TGGGCATGGTGGCGG | 1130 |
rs182299586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863814 | TGTTTACTACTAATA[A/G]TCTCAGCTTTGACAA | 1130 |
rs182305277 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235781411 | TCTAACTAAAATTTG[A/C]ATCAATATCTTTATT | 1130 |
rs182306435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826917 | CGAACTCCAGGCCTC[A/T]AGTAATCCATCTACC | 1130 |
rs182308603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235861165 | TATTTCTTCCATTCA[A/G]TTAAAATAGTGAAAA | 1130 |
rs182309921 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235819613 | ACCCAATCAAGAGAA[A/C]TCAGCCAATAACATA | 1130 |
rs182316217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862445 | CATCCTGCCCTATAG[C/T]GTATATAGGATTCAG | 1130 |
rs182316335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845408 | AGGGTGGCTAGAGGA[G/T]CAGGGGGTAAAACCC | 1130 |
rs182318237 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662211 | TAGTCAATATCTAGC[A/G]TTACAGATTTTAAGT | 1130 |
rs182331021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235880917 | GATCGCCAGAGGTCC[A/G]GAGTTCAAGACCAGC | 1130 |
rs182357114 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235723975 | TATGAGTATAGTTAC[A/C]GTGGCCCATGAGCAC | 1130 |
rs182363139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714696 | AGGCCTCCAGTCTGT[C/G]ACTTAAAATGCTGAT | 1130 |
rs182365403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692618 | TGAACTCCTGACCTC[A/T]GGCGATCTGCCCGCC | 1130 |
rs182365741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691416 | AGGGCTTTAGGCCCA[A/G]TGTTCTTTCTACTAT | 1130 |
rs182379798 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235794875 | AACTGAGAGGTTCCA[G/T]TTAAAAATGGGGAAA | 1130 |
rs182392669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828121 | ACAGACTAGCAAAAT[A/G]TTCCCAAAAGAAAAA | 1130 |
rs182397302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766453 | ATTTCCTAATTCAAG[A/C]AATCTTGTTATTAAA | 1130 |
rs182415886 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235871805 | CAAGAATCTGCTCTC[A/G]GGGTCTGGGACAAGA | 1130 |
rs182558970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843390 | TAGGACCCAGAAGCC[A/G]CAGATCAGGAATCTA | 1130 |
rs182570678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879801 | GAGTGCAGTGGCACA[A/G]TTTTGGCTCACTGCA | 1130 |
rs182586307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790258 | TAGCTTATAGTATAG[G/T]AGCAATGTTAAGGCT | 1130 |
rs182605887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736561 | GAGGGTCAGCAGGCT[A/G]GAGAGTTAATCAGAA | 1130 |
rs182608961 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235836795 | GTTTACTGATAGGTA[A/C]GACTGACATAAGAAC | 1130 |
rs182618772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235872357 | TCAGAAATGAAGACC[A/G]GAAGACCCAGGGAAA | 1130 |
rs182629505 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235669922 | CAGAGTGGGGGGTGG[A/G]GATTGACCTATGTAA | 1130 |
rs182632019 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235849004 | AGAGGGAACCCTACC[C/T]AATTCATTATATGAA | 1130 |
rs182632348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235675889 | CTCTGGAAAAACACC[A/G]TACATTTTGTGTTAG | 1130 |
rs182635085 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867355 | AGGTCTAGAGGATGA[A/G]GATAGAAGAAATAAC | 1130 |
rs182639651 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235710631 | CATTTCCTGTCTTGC[A/T]TGCCCTTCCAGAATC | 1130 |
rs182640785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235731446 | TTAAATTTTTTAAAA[G/T]ATATGTAATGACTAC | 1130 |
rs182660860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749108 | GACAGAAATAGAAAT[C/T]CCTCTATGTCCCTTT | 1130 |
rs182661271 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772618 | TGCTGAGATGTAGTG[C/T]CTACATCTAAGATCA | 1130 |
rs182664993 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235703424 | CAAAGCTCTTAAATG[C/T]AAAGGGTATTATTGT | 1130 |
rs182668579 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771993 | TTTGGGAGGCCAAGG[C/T]GGGAGGACTGCTTGA | 1130 |
rs182676743 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235730533 | TGGGTATATATATAT[G/T]TACCCATATATGTGT | 1130 |
rs182677607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235689664 | ATTCTCATCACACAC[A/G]TAAAAAATGCTAACT | 1130 |
rs182700647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699165 | TGTTACATAGGTATA[C/T]GTGTGCCATGGTGGT | 1130 |
rs182708194 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235695944 | CCAGCCTACTGTACT[C/G]TAATTTTTTAAAGGT | 1130 |
rs182718383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696776 | TTGTTGGTCAAATAC[A/G]TCTGTCTATTCTGGG | 1130 |
rs182718676 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235681105 | AAAGAACTCCGGGGA[C/T]CCACAGATAAGTCGC | 1130 |
rs182724436 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662570 | GTTTTATATAAACAA[C/T]CAACCAACCAATTTA | 1130 |
rs182737610 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235732404 | AACTCCTGGGCTCAA[C/G]TGATCCTCCCGCCTC | 1130 |
rs182747659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780410 | TCCTGTCTCTTAAAA[A/T]AAAAAATAAAAAATA | 1130 |
rs182750414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235711414 | TACAACAAAATTCCA[A/G]TGTAATTTGCCCAAC | 1130 |
rs182813919 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235785598 | CCTAGCAAAAGGTCT[A/G]CAACATAGTAAGTAT | 1130 |
rs182820459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235852247 | ACAACTCATGCCTCA[A/G]TGGGAAAATGAATTC | 1130 |
rs182821043 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235822210 | TATATTATGGGCTAA[C/T]TGTTATAGAAAAGAG | 1130 |
rs182826228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805214 | CAGAAGAGGTTAGGA[C/G]AAGAATCTGGACAAA | 1130 |
rs182890563 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235814557 | ACCAGTTCAGGAAAG[A/G]AAGGAGTCAGCAGGG | 1130 |
rs182892891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853184 | TTGTACATTTATACC[A/C]AAAAGTAAATGACTT | 1130 |
rs182899751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235781100 | TTAAAACACCCTAAC[A/C]AGAATTTTTCATAAA | 1130 |
rs182901137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739712 | CTGATGGAATGAGAG[A/G]CTTAGAGAAATCACT | 1130 |
rs182904574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749256 | AGATACTTTTAAGTA[A/G]TAGTGGAGAAATAAA | 1130 |
rs182904700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235830122 | AATGTGAAAGACTGG[A/G]CTTTATCTCAAGGAG | 1130 |
rs182912429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848857 | CTGAACAGACCCAGC[A/G]AGATTGAAATGGTAA | 1130 |
rs182912531 | snp | A/C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867152 | GACCCGCGGGGCTGC[A/C/T]GCCGGGGCCCGGTCT | 1130 |
rs182918998 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235711013 | GAAGGCAACAGCATG[A/G]GACACCCTGAGCTAA | 1130 |
rs182939522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818992 | GATTGCTGTTCTCCC[A/C]CTCAAGAGAAAGGAA | 1130 |
rs182949277 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235790819 | AGAAGGAACTGGAAT[A/G]AAATTTATTCTAATG | 1130 |
rs182966607 | snp | A/G | 6.59185e-05 | 0.00574064 | intron-variant | LYST | GRCh38.p7 | 1:235755462 | CCAATTATAGTGGAG[A/G]GAAGAACACACTTAC | 1130 |
rs182968222 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235776945 | TGTAATTTTTTTATG[G/T]TAAAAGTTTAATATA | 1130 |
rs182969517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235680489 | CTGGTCTCAAACTCT[C/T]GGCTTCAAGTGGTCG | 1130 |
rs182992238 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235680709 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCTTCCTG | 1130 |
rs183122188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674279 | CCAAGCGGATGTATG[G/T]TAGTATTGTAGTGGA | 1130 |
rs183144325 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706333 | CCTGTAGTAAAGAAG[C/T]ACCCTCATTTCAGAA | 1130 |
rs183151142 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LYST | GRCh38.p7 | 1:235725334 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATCA | 1130 |
rs183154857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692206 | AGTGTGGTGGCACAT[A/G]CCTGTAGTCCCAGCT | 1130 |
rs183155723 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235776479 | CAGGGATGTGGATCC[A/G]GAGGAAGTAGAAATG | 1130 |
rs183164677 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235755245 | ATACAAAAAACTAGC[C/T]GGGCATGGTGGTACG | 1130 |
rs183174366 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761986 | TGTCGGGTGGGGGGA[G/T]GGGGGAGGGATAGCA | 1130 |
rs183199092 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235801421 | AACTTTCTGACCCCC[C/G]CCTCAAATACCTAAA | 1130 |
rs183202780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684919 | CAGGCATGAGCCACC[A/G]CACCCTGCTTATATT | 1130 |
rs183216261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835162 | CTTCAGGTGATCCAC[A/C]CGCCTCGGCCTCCCA | 1130 |
rs183217744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235858234 | TCAGGTACTTCGTAG[C/T]TGTGAGTCTTGGGAA | 1130 |
rs183219654 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235831089 | CATGAACAACGAAAT[C/T]CCCAAGGAGTTTCAA | 1130 |
rs183223255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737446 | AATGACAACCCAGGA[C/G]AAATAAACATACCTA | 1130 |
rs183229578 | snp | A/C/G | 3.29991e-05 | 0.00406185 | intron-variant | LYST | GRCh38.p7 | 1:235720633 | TATGGATGGATGAAC[A/C/G]CTAAAGGTGATGATT | 1130 |
rs183229999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235695696 | GGAGTGCAATGGTGC[A/G]ATCTTGGCTCACTGC | 1130 |
rs183230507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235699590 | TTCCTTTGAGTATAT[A/G]CCCAGTAATGGGATT | 1130 |
rs183232576 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715047 | TACTACAGCTTTTTT[G/T]AGGAGCACTTTGGGC | 1130 |
rs183258194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721743 | TAGCGCTAAGGTCCA[C/T]GGAAGGGGATTTATG | 1130 |
rs183261972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841398 | AAGAGGTGGTGCGGC[A/G]TGGCCAGCCATCTCC | 1130 |
rs183262171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822552 | CCAGAACTGATGCAT[A/G]CCATGAGATCATCAA | 1130 |
rs183270911 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235858583 | CTTGACTCATTTAGA[G/T]TCTTCATCCTCTTCA | 1130 |
rs183272516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876865 | ATTTAGATGGTACGA[A/G]TTATACGGGTCCTGG | 1130 |
rs183296507 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661834 | TGGGAGAGACAGACG[A/G]CTCCAAGATGTTTAG | 1130 |
rs183314541 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689023 | TAATAATAATAATAA[C/T]AATAACAACAACAAC | 1130 |
rs183320106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805310 | CCCACAATGATTGTC[C/G]CCACTTCTTAGAGCC | 1130 |
rs183420109 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235818198 | AGTGGCTGAAACATA[C/T]ATACCAAGAGGGAGA | 1130 |
rs183426002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799595 | AAAGTCTCGTGTAGG[C/T]TAGCCTTAATTCTCC | 1130 |
rs183427625 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235749675 | ATTTACTTAGAGTGA[A/G]AAAGACAAGTCCAAG | 1130 |
rs183427803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834536 | AGCCACTGTACCTGG[C/T]CCAGGAGTGATCTTT | 1130 |
rs183437395 | snp | G/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235840573 | ACCCACAGCAAGACC[G/T]AAACATCGGTATTTT | 1130 |
rs183439330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840934 | GAGGGATCAGGACAA[C/T]TCTCTGAATACTGGC | 1130 |
rs183441308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870822 | TAAATAGTTAAATTA[A/G]GAAAATTTTGTTGAA | 1130 |
rs183442894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235851517 | AATAACTTATTCATG[C/T]AACCAAATACCACCT | 1130 |
rs183460111 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235876677 | CATCCTGTTTGTTAG[G/T]AAAGTTCTGTTTTCT | 1130 |
rs183484782 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702569 | CAAAGCACTCTCTCA[C/T]ATCGCTAACACAGCA | 1130 |
rs183488601 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235767246 | CTCTTCATATGTCCA[A/G]ATATATATCTCTACA | 1130 |
rs183494622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737672 | TTGAATCTACAGAGG[C/T]GTTAATTTTAATATC | 1130 |
rs183496901 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739164 | GTAAAATCCTACAGT[A/T]TATTCTGTAGGTACT | 1130 |
rs183497950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699765 | GACTTTTTAATAATC[A/G]CCATTCTGATTGGTG | 1130 |
rs183519456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235804094 | ATGATTTAAAATTAA[C/T]GTGAGTAGAGAGTTC | 1130 |
rs183555575 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669648 | ACTTCATTCACATGA[C/T]GTGAGCATAAAGTGG | 1130 |
rs183589546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863637 | TGTGAGTGCAATCAA[A/T]CAAAAATAAAACTAC | 1130 |
rs183591242 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235846267 | GCTAGACCCAGAAGA[C/G]AGACAACAATCACTG | 1130 |
rs183601628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882770 | AGTCCATGTTGGAGA[C/T]GTTCAGTTTCATGTG | 1130 |
rs183607611 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235667157 | ACATCAACTAAAAGT[C/G]AGAAACCTAGGCATT | 1130 |
rs183646638 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235700146 | CCTTAGAAGAAAATC[C/T]AGGCAATACCATTCA | 1130 |
rs183647861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686338 | TGCCATTGCATTCCA[A/G]CTTAGGCAAGAGAGG | 1130 |
rs183706826 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884755 | TTAATATTTTTATTT[A/G]GAAACTTTTGTACAT | 1130 |
rs183713486 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885015 | CAGGCTGGTCTTGAA[C/T]TCCCAGGCTCAAGCA | 1130 |
rs183728846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715498 | CTCCCACTCTTACCC[A/C]GGAGACTTCAGCCTC | 1130 |
rs183740525 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | LYST | GRCh38.p7 | 1:235743471 | ATAGAGTAAACTGAC[C/G/T]GATTTGTTCCGTTGT | 1130 |
rs183758565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785134 | CCCTGTCTTCCACCT[C/G]AAACTGTCCTCCTCC | 1130 |
rs183766345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821619 | TTTTTCTTGAATTAG[A/C]CCAGGAATTGCAACC | 1130 |
rs183795014 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235685316 | TCCTGCCTGGATCAC[C/T]GCGGTGGCCTTCTCG | 1130 |
rs183799328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235786563 | GGTATATACCCAAAG[G/T]ATTATGAATCATACT | 1130 |
rs183802370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814152 | TTCAGCATCTAGGTA[A/G]CTGATAATGTATTCA | 1130 |
rs183808098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848398 | GGTGCTAAGAGGAAA[A/G]TTCACAGTCCTAAAT | 1130 |
rs183840824 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235704487 | ACTGTGGTTTTGATT[G/T]GCATTTTTCTATTGA | 1130 |
rs183845857 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235682166 | AAATTTAAAAAGTAG[C/T]AGGGCATTGTGGTGT | 1130 |
rs183849355 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235811426 | ATGCCAAATGTTCTC[G/T]AAAACTGAGGTTTAA | 1130 |
rs183853686 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235663231 | ACTCATTGGTTTTGA[A/C]TGTAATTCTAACATA | 1130 |
rs183855600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690010 | ACACCACATCAATCT[A/C]ATGTAACAGTACCCA | 1130 |
rs183861505 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235845653 | AGTTAGGGGGGACAC[A/G]GTGGGAGTGAGAGTG | 1130 |
rs183863192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827849 | GTATTCTATTTACCA[C/T]ATATACAAAGAAAAT | 1130 |
rs183871514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762242 | GATCATATGGATAGA[A/G]CAAAGCGGGATATTG | 1130 |
rs183877968 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235722401 | AGGAGAGCAGAGAAA[C/T]GGTAGTGAAGGGACT | 1130 |
rs183878469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863166 | TGGGGGCCGAGGAGG[A/G]CAGATGATGAGGTCA | 1130 |
rs183882731 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740470 | CCTGAATTCTATCGT[A/C]ATATCTTGGTTTTGC | 1130 |
rs183891109 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | LYST | GRCh38.p7 | 1:235691165 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 1130 |
rs183896711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235733364 | TTCTTTAAGATGAAA[A/G]AAACATCACAAATGA | 1130 |
rs183905946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866266 | CTGGAAAGAGAGGCT[C/T]TCGCCCAGTCAAAGG | 1130 |
rs183906264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235673481 | CATATGTTGTTTAGA[C/T]CACCAAAAATCAAGG | 1130 |
rs183911269 | snp | C/T | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773967 | TATAAATAATATCTT[C/T]ACCACAGCATCCTTC | 1130 |
rs183923178 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792883 | TGGTCAGGCTGGTCT[C/G/T]GAACACCTGACCTCA | 1130 |
rs183923522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750471 | AGATTTGAACTTAAG[G/T]GAATTTAAGACAGTA | 1130 |
rs183939471 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235723586 | AAATGGGGACAAAGA[A/C]AGATTATGACATTAC | 1130 |
rs183976397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795506 | AAAGACACTATACGC[C/T]AGCCAAGCCCTATAT | 1130 |
rs183981956 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235726549 | ACACACATTTGCACA[C/T]ACAACGCAAGATACC | 1130 |
rs183997520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862937 | TATAAAATGAGGTGT[C/T]GCCTGATTCTACAAT | 1130 |
rs183997865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767929 | TTCTTCCCCCTCTGC[C/T]GACCTCTGGCTTTCA | 1130 |
rs184003487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235829954 | TTCTACTAAGAACCA[C/T]AGTTATCTCACTGAT | 1130 |
rs184072099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791570 | CAGGACCTACCACCA[C/T]TAAGTAAGGCATTTA | 1130 |
rs184080634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827497 | AAAACTAAATTTCCT[C/T]CTAAAACATACAACT | 1130 |
rs184095583 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842233 | AAAAGAAAGAGGCCA[A/C/G]GAAAATAAATGTTGA | 1130 |
rs184101412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235823758 | TGTTTCCTGCCTCTT[C/T]ACATCGCCAATTCCT | 1130 |
rs184129750 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235729037 | TCAGGGTTCTCACAC[A/T]TGGAGAACCTAGCCT | 1130 |
rs184139267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235716357 | ATGGTTATGGGTACA[C/T]TATAAATATATTAAC | 1130 |
rs184152715 | snp | A/C | 0.000679117 | 0.0184146 | intron-variant | LYST | GRCh38.p7 | 1:235747371 | ATATCAATTTCTATA[A/C]ATAACCTCTACAAAA | 1130 |
rs184155919 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235787659 | AAATATATATTATTA[C/T]TATTTATATAGCCAT | 1130 |
rs184160931 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235881012 | GTGCATGTAATCCCA[A/G]CTACTCAGGAGGCTG | 1130 |
rs184166983 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235769774 | GCATATAAAATAGAC[C/T]GTTAGCAAGTTTATA | 1130 |
rs184222139 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772905 | CCAGCTCAGCATTCC[C/T]CATGGCTGTTCAAAA | 1130 |
rs184235900 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235810660 | ATGTATTTTGCTGCA[C/G]GGCTGATTTCCTTCA | 1130 |
rs184237667 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235845564 | AAGCCCTTTTCTTTC[A/G]TAGCTGAGAGGTGGA | 1130 |
rs184333461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235874042 | ACTTCAAAGCAACAG[C/T]TGAAAAGGGTGACTC | 1130 |
rs184353846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774448 | GCTTTCATCTAGAAA[C/T]GTATTTAAATATATG | 1130 |
rs184364067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734280 | GATAATGGATACTGA[C/T]GACCACAGAGAACAA | 1130 |
rs184377930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235811797 | CCCAAGCAAAAGATG[C/T]AGACAATGAAGACAA | 1130 |
rs184386310 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235677390 | TAAAATGATTATAAC[A/G]TAAAGACATTATTTT | 1130 |
rs184387819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693885 | CTGTTAGTAGCAGGA[A/G]GATAACACTGCTAGA | 1130 |
rs184407136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726891 | CATCTTTTGGACATA[C/T]AAAAAAGTTGTCTCA | 1130 |
rs184411941 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746370 | GACTGCTAAAACAGT[A/G]AGCCTCTGTAGTCTC | 1130 |
rs184413268 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235707580 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 1130 |
rs184418918 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235671956 | GACTAGTGTGATAGA[C/T]GTTAGGGTAGGAGAA | 1130 |
rs184443731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697774 | CATCTCAAATAGATA[C/T]GTGATGAGTGAAAGG | 1130 |
rs184487674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833204 | AAATATTGAATTTAA[C/T]TGAATGACTTTCAGT | 1130 |
rs184498890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235751888 | TGATAGATACTATTA[C/T]AAAATTAATGTTAAA | 1130 |
rs184505764 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235869238 | AGCACTTTGGGAGGC[A/C]GAGGCGGGCAGATCA | 1130 |
rs184507851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235850090 | CTAAGTGAAAAGAAC[A/G]AATCTGGAGGCATCA | 1130 |
rs184510661 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235793957 | CCTGCCTCAGCCTCC[C/T]GAGGAGCTGGGACTA | 1130 |
rs184516504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828004 | ATATACAAATGGCCA[A/C]TAAGCAAATGAAAAA | 1130 |
rs184522654 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842667 | TTAAGCCCCTCGTAG[C/T]CAAGTTAGGTCAAAG | 1130 |
rs184524748 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235860311 | AGCCCCCCTAAACTG[A/G]TACATTTGTTATAAT | 1130 |
rs184529538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879496 | CAGACACCTGACAAC[A/G]TGTGTGGAGGACACT | 1130 |
rs184551829 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713033 | AACACATCTTTTCAT[C/T]TGGAGACTGCCACAA | 1130 |
rs184563930 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235778377 | TCTTATTATTTATTT[A/C]TTTATTTATTTTTCC | 1130 |
rs184570254 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | LYST | GRCh38.p7 | 1:235816065 | AACCCGGGAGGAGGA[A/G]GATGCAGTGAGCCAA | 1130 |
rs184581131 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235798788 | AAAATATCCAGAAAA[A/G]GAAGTAGATGAGTGA | 1130 |
rs184608470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824663 | TCCCCTGAGAATAAG[C/T]AGATTAAAATTTCTG | 1130 |
rs184623453 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782419 | ACCTCATGATCCACC[A/C/T]GCCTTGGCCTCCCAA | 1130 |
rs184633258 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235819889 | CTGACCTCGTGATCC[A/G]CCAGCCTCAGCCTCC | 1130 |
rs184637602 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235882012 | TAAAAATGGGTAAGA[C/T]GATAAATTTTATGTT | 1130 |
rs184643457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854548 | ACTGGTTCACCTCTG[C/T]ATCTGCTGCTCTATG | 1130 |
rs184650691 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712691 | TCTTTCTTTCTTTTT[C/T]TTCGGGGGGGTGCGT | 1130 |
rs184680999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235741872 | CTGAACGTCCATCAG[C/T]GGATGAACAGATAAA | 1130 |
rs184693156 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235873620 | ATTGAAAAAAGAGAG[A/T]TTTGGGTCTATTATT | 1130 |
rs184732632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681608 | AAAGGAATGAGCTGG[A/G]GCAATGGTCAGGGGG | 1130 |
rs184749043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764446 | ATTTCATTTGGACAT[G/T]TACTGCTGCTTATTT | 1130 |
rs184751075 | snp | C/T | 1.66835e-05 | 0.00288816 | intron-variant | LYST | GRCh38.p7 | 1:235802892 | TCTAATTACAAGCAC[C/T]TCAATGATATTTTAC | 1130 |
rs184764836 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235797695 | AAACTTACGGGGAAC[A/G]TTCCATAATATTGGA | 1130 |
rs184772418 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | LYST | GRCh38.p7 | 1:235778121 | TATATATATATATAT[A/T]TTTTTGTAGAGACAT | 1130 |
rs184790829 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235838555 | TCTCTAGAGTCTTTT[G/T]TGGAAGTAACATCAA | 1130 |
rs184806594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697345 | CTTCTAATTTAAGCT[C/G]TAAACAAAGTAAGAG | 1130 |
rs184814617 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235700612 | TGTTTGCATTTTGTG[C/T]AGATGTCAAGTGAAG | 1130 |
rs184822836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717133 | AGCCCTGAAAGTTAG[C/T]GTCCCATTTTCCAGA | 1130 |
rs184829891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235686540 | AAGTGGTACAAATCC[A/G]GACAGACTACTTAGA | 1130 |
rs184840106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235757535 | AGGAACTGTGACAAG[C/T]AGTAGCATTTTTTAA | 1130 |
rs184862112 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738171 | GTCATGGAAGACAAA[C/T]TGAAGGGCGAGATGA | 1130 |
rs184877695 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662677 | AATTTTAAGAATATC[A/G]TTTTAATGTACCATG | 1130 |
rs184900947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859869 | ATGGGAATGTACTCT[C/G]TAAGTTATAAAGTAG | 1130 |
rs184942876 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235694346 | ACATAGTATGATGTT[C/T]TCTTGGCATAAAAAT | 1130 |
rs184948017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756396 | CACAGAATTTCTTAC[A/G]TTTTACTTAGTTAAG | 1130 |
rs184958291 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235795829 | TAATATTTAAAAAAC[A/C]AAAAAACAGACAAAA | 1130 |
rs185006525 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235690865 | TACAGTCTGGAACGG[C/T]TGCAGCAGCATACTG | 1130 |
rs185013607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838036 | GAAGGAACAGTGGCA[A/G]TTCATCTAATTGAAT | 1130 |
rs185017692 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235794958 | ACAGAATTATAAGAA[A/G]GAAGAAATCCGTAAC | 1130 |
rs185019938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819674 | TGTTTTGAGATGGAG[G/T]CTCACTCTGCCACCC | 1130 |
rs185023277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878735 | TCTAATAGGAGAGCA[A/C]GGGTTTCCTGATGGG | 1130 |
rs185035567 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853849 | AAACTTAAGCCTTTC[A/G]ACAGGTAGTTCATTT | 1130 |
rs185036760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820294 | GGCTAGGGTTCAAGG[A/G]CTTCTGGATGACATG | 1130 |
rs185039640 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235872579 | AGGTCTTATGACCTA[G/T]AATCATCCAACAGGG | 1130 |
rs185041038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235803409 | AATTTAATACTAATA[C/T]ATATTATTTGTGCAC | 1130 |
rs185045078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839227 | TATTCTATAGGTTTT[A/T]TATGTGTGGGTGTAT | 1130 |
rs185050073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235777896 | TTCTCTAAACTATTT[C/T]AAAAATTAAAGTTAA | 1130 |
rs185052147 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737895 | TTAAAGGTAGCGAAG[A/G]TGCTGGAGCCGCTGC | 1130 |
rs185054797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708391 | CGGAAAAGAGTTAAC[A/G]TAGCAAGATTGACTG | 1130 |
rs185080284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723907 | CTTCACTTTAATCAG[A/G]ACTAAGAAACATGGC | 1130 |
rs185081812 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235815475 | TCCATGAAAAGATTT[A/G]GAGGAAAAGGGCTCC | 1130 |
rs185086579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235699308 | TGTTCTCATTGTTCA[A/G]CTCCCACTTATGAGT | 1130 |
rs185088279 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235683966 | TTAGATTTTTTGGCA[C/T]TGTTAAATAGTAACT | 1130 |
rs185091096 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235752760 | GTACGATATTAGGCC[C/T]ACAATGCTTCTCTCC | 1130 |
rs185092973 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235781802 | TAGATGGATATTTTA[A/G]CCAGGTTAATTTACT | 1130 |
rs185099858 | snp | A/C/T | 6.67249e-05 | 0.00577569 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774998 | CAATTTTCTAATTCA[A/C/T]GTACTCTTTGTTGGT | 1130 |
rs185100835 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235665706 | CTTAATTCTTAAAAA[A/C]AGAAGAAAAAGTATT | 1130 |
rs185102725 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235705567 | ATTTTTAAATTTTTT[A/G]TAGAGACAGGTTCTT | 1130 |
rs185108060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802225 | AAAAAAAAAAACTAG[C/T]AGTACTGGGACACTC | 1130 |
rs185115627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704918 | TTTAAAATAGTGCTT[G/T]TCAACATTCTGTGGT | 1130 |
rs185117108 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235742690 | TTAAAAAAAAGCATC[A/G]AAGAACAATGATAAA | 1130 |
rs185123087 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235784137 | CTTCTGCCTCGGCCT[A/G]TCAAAGTGCTGGGAT | 1130 |
rs185125017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765465 | GACCTATAACTAGAA[A/T]ACAAGTTCGAATTCT | 1130 |
rs185129869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235672791 | CACTAGAAAGATATC[A/G]GCTTATCCCCGTATA | 1130 |
rs185130275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877738 | AAACGTTTCTATTCC[A/G]TGAGTACAGTTCTGA | 1130 |
rs185173153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738754 | ACACATCCTGGGCCA[C/T]TGGACTCTCTGTGGC | 1130 |
rs185217865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235841787 | GAAAACAGGTGGAAG[C/G]CCAGAAACTGAGGGA | 1130 |
rs185218339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865743 | ACATCTTTATTAGCA[C/T]AGATGAATCTAGGCG | 1130 |
rs185239293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858984 | AGCAAAGAAGTCACA[C/T]GCCCCTAGTTAAGTC | 1130 |
rs185252704 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235701497 | GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAATCCC | 1130 |
rs185295734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758088 | CTGGGTTTAGCCCAG[A/G]TGAAACTTCTGGAAG | 1130 |
rs185297402 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235718492 | GTCTCGAACTCCTGA[C/T]GTCAGGTGATCTGCC | 1130 |
rs185308472 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | LYST | GRCh38.p7 | 1:235786838 | CTCACTCATAGGTGG[C/G]AATTGAACAATGAGA | 1130 |
rs185312607 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235823073 | AATCATTGTTTTATG[A/C]CACTAAGTTTTGGAA | 1130 |
rs185427949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235815904 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACAAGGT | 1130 |
rs185435523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849566 | CAAGTCAGTAAAGAG[G/T]AAGTCAAACTTTCAC | 1130 |
rs185474493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707151 | TCATTTGGACTCTAC[C/T]ACTACATCCAGGCAG | 1130 |
rs185518805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829454 | CATCATATTGGTGTT[A/C]CAAACACTTCATTAT | 1130 |
rs185526635 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235847646 | TCAACTATCTATTGC[C/T]TTCAGGATACTCACC | 1130 |
rs185528676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864832 | TACTTCAGAGGCTGA[C/G]GTGAGAGGATCACCT | 1130 |
rs185546119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676402 | TGACACATAATCAAA[C/G]TGAACTTGGAAATGG | 1130 |
rs185564006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235753917 | AAATTCTTTAAGGTC[C/T]GAATTTGTCTATCAC | 1130 |
rs185569095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832312 | CATTGCAAGATACAC[C/T]GCAACTTTAGAAACA | 1130 |
rs185582443 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235795089 | AACCTAGAATTCCTT[G/T]GAATTACAAAGAGGT | 1130 |
rs185586653 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235767340 | TGAAACAATTTAGTT[C/T]GACTACCTCAGATTT | 1130 |
rs185587253 | snp | C/G | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868398 | AAACTTAACCTGTTT[C/G]GTCATTTTACCTAAA | 1130 |
rs185597337 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235775545 | ACCAACACTTTCTGA[A/C]AACTACTATATACAT | 1130 |
rs185599409 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235813156 | CCAAAAAATCCTTTT[C/T]CTTGAAAGTCTGCAT | 1130 |
rs185605358 | snp | C/T | 0.000628369 | 0.0177141 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744080 | TTTCCTCAGAAATTT[C/T]GGTCTGGAAAACTGA | 1130 |
rs185629625 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235688323 | AATTATTCCTAAATA[C/T]GCAAAAAACAAACAA | 1130 |
rs185662660 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235701876 | TGAACATTTGACATA[C/T]GTGAGCTATGAGCGC | 1130 |
rs185663512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235693143 | ACACGATGAAATCCC[A/G]TCTCTACTAAAAGAA | 1130 |
rs185667536 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235668073 | TAATAAGAAAAAAGT[C/T]TGTACATACTAAGTA | 1130 |
rs185668886 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235718792 | TGCTGAATTCTGTTC[C/G]TTTAATTGCCAAATT | 1130 |
rs185669795 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828210 | TTTCATGACATAAAA[A/G]AGAAAGCATAAAATC | 1130 |
rs185692914 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235863850 | CTTTGCTTGGCCAAA[C/T]TTACTCAGGCTTTTG | 1130 |
rs185714521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235763658 | GAGACGAGGTTTCGC[C/T]ATGTTGACCAGGCTG | 1130 |
rs185726445 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722957 | CAGGAAGGCCAGTTA[A/G]GAGGCTACTGTAAAT | 1130 |
rs185740054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882860 | TAACTACGCCATGAC[A/C]CAGACAAATAATCTC | 1130 |
rs185752924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235869447 | ACTACAGTCTGGCCC[A/G]GGTGAAAGAGCGAGA | 1130 |
rs185754617 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235844561 | TTCTTCTTCTGTCGA[G/T]TAGAAATTAGACAAC | 1130 |
rs185756820 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826822 | GAGTAGCTGGGACTA[C/T]AGGCACACACCACCA | 1130 |
rs185772348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862068 | CATGCTGAAGTTCCA[C/T]TTCACCAAGCCAAAA | 1130 |
rs185780352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851693 | TTATAATCTATTTTA[C/T]AGTGGATAATAAATA | 1130 |
rs185786651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871231 | GGTTTTAGTATGATT[C/G]TTTCATGTAATTTTC | 1130 |
rs185804333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749238 | AAGCCAATATACTTT[G/T]GAAGATACTTTTAAG | 1130 |
rs185804811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235812431 | AGAATTGCTTGAACT[C/T]GGGAGGCTGAGGTTG | 1130 |
rs185824403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790488 | AAATATTATCACATG[G/T]AGAGCTATCAGTTCT | 1130 |
rs185836240 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235741052 | TTTTTGAGATATGTT[A/C]TATATACTGTTGTTT | 1130 |
rs185836332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772149 | AGGACCACTTGAACC[C/T]GAGAGGCAGAGGTTG | 1130 |
rs185843987 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809522 | AATGAATTCTTGAAC[C/T]AAATCCATGGCTTGA | 1130 |
rs185849427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799840 | TACTTGCACTCTGGC[C/T]ATTTCATTGTGTGGA | 1130 |
rs185863811 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235818206 | AAACATACATACCAA[C/G]AGGGAGAGGGCTAGG | 1130 |
rs185909973 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235775827 | CCTCTTTGGCTGGAT[C/T]GTAGAGACCAGGTTC | 1130 |
rs185921743 | snp | A/T | 0.000399281 | 0.0141238 | missense | LYST | GRCh38.p7 | 1:235664579 | ACATGTCCAACGAGA[A/T]CCCCGTTCACCGTCC | 1130 |
rs185938931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235813845 | AGTAAAGGATTTAAC[A/G]ACAAATCAAGTTTGA | 1130 |
rs185987123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235736850 | GTATCTTCAACAGAA[A/G]AAAAAAGTCAGTTAC | 1130 |
rs186037645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235673923 | ACCTTAAATAAAAGC[A/G]ATTGTTGCGCTTTTG | 1130 |
rs186055813 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235795378 | AACAAACTGCCTAAC[A/C]AAAGGGAAAAGTAGA | 1130 |
rs186059966 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235829551 | ATTATTCATTTTCTA[C/G]TAAAATGAAATAAAG | 1130 |
rs186062091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235855170 | ACTGTATTGTTTCTT[A/T]TAAAACTAGATTATA | 1130 |
rs186062982 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235818038 | GTCAATTTTGCAATG[C/T]ACATCTTTCCAGAAA | 1130 |
rs186104199 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235710036 | TTACCTTTAAACAGA[A/T]ATGGCTTTTTGTGCT | 1130 |
rs186114283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695616 | CAACAGAGAGAAACT[G/T]TACAGTACTCTAATT | 1130 |
rs186114459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235679251 | ATTCTGGCTCTCAGA[C/T]TGTGACACTCTCCAC | 1130 |
rs186115566 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719744 | AGTCTCTAGGAAATA[C/T]AGGGGTTATGGGAAC | 1130 |
rs186120879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754764 | TAAGAGTGAGTTCAC[C/T]AAATTTTACATTTAA | 1130 |
rs186121674 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739046 | AGGATTTTAGTTGGA[G/T]GTTGTGCATATTGTC | 1130 |
rs186123540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702104 | CCTTCTGCAAACCCT[C/T]ACAGTGCTTACAATT | 1130 |
rs186126160 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235771768 | ACTTTTCTCTGTTTT[C/G]TGGCTGCATACTCTT | 1130 |
rs186130371 | snp | A/C/T | 3.38663e-05 | 0.00411488 | intron-variant | LYST | GRCh38.p7 | 1:235729700 | GACTAAATGTTCTGA[A/C/T]CAATTTCAGAGAGGA | 1130 |
rs186132900 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714753 | CCACAGTGAAGTTGC[C/T]GGTGTGCGTCTTTTA | 1130 |
rs186141121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748849 | AGGGCTTGAGTAAAT[C/T]TGTCTATTATCAGAG | 1130 |
rs186148683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235799385 | AAGGGAAAATAGTAA[C/T]TTTACAATAGAGAAA | 1130 |
rs186152859 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759135 | TTGCAATAGTGCTGT[A/G]GCTTCGCTGGAAGGA | 1130 |
rs186154983 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235779997 | ACCACTAGCTCCTAC[A/T]TTATATACTGGTAGA | 1130 |
rs186162492 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235785183 | TCCATCTCCTCCTTC[A/C]GGTCTCAGGTTTAAT | 1130 |
rs186165941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691357 | GTTACTAGTCAAAGG[C/T]TGCAGTTAGTATATA | 1130 |
rs186166678 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821681 | TTAGACTTGGTGAGT[A/C/T]ATATATGGTCTCTGT | 1130 |
rs186176907 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661217 | ATTTTTATTTTTACA[C/T]AAAAATATAATATTG | 1130 |
rs186183703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858126 | GACTTAATGCTCTTT[G/T]CCTTCTTCTTCAATG | 1130 |
rs186220471 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235714223 | TATTTAGTACAAAAC[G/T]GTCCTATTTATTTTT | 1130 |
rs186296122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804850 | TAAAATTAATAACAT[C/T]TTTATTGATAAAATA | 1130 |
rs186299301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682638 | AACCATAGAAATGTA[A/G]TCGGATGAAAGAATA | 1130 |
rs186327333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235856885 | AATATGAAAAGTAGG[A/G]TAAGAGTGAGCTGAT | 1130 |
rs186332797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874842 | GTTGTTATTTGTATG[A/G]GCGTGTGTGTGCATA | 1130 |
rs186337941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840829 | TTTTTTTCTAAAGCA[A/G]CAGTAGAATAATATA | 1130 |
rs186361277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678704 | CATTGTACATATAAT[G/T]TGTGTACTGTTCTAC | 1130 |
rs186385731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736117 | TTAAGTTGTTTCTAA[C/T]ATCTCATTTTAATAC | 1130 |
rs186411549 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235839630 | GAACCCCCCCCACCA[C/T]GCCCCATCTCTACTA | 1130 |
rs186411626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821247 | CTTGAAAACAGTCTG[A/G]GCAACACGGTGAAAC | 1130 |
rs186435224 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235698983 | TGCCAGGAATTCATA[C/T]AAAAGGAACTTCCTT | 1130 |
rs186459953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665102 | CCAGGCCAAGTTGCA[C/T]AGATCTTTATGTATT | 1130 |
rs186481035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758329 | TGGCTGAAGAAATAC[A/C]ACGCCTAGGCAATGT | 1130 |
rs186481998 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235799302 | CTAAAATTAGTGGAT[A/G]AAAGAATGAGAAAAA | 1130 |
rs186490124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833810 | GAGCACACTAAAAAA[A/T]TGCCTACTTCAAGAA | 1130 |
rs186520638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235695793 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTTTT | 1130 |
rs186558563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698539 | TGTCTAACAGTGTTT[G/T]TTTGTGGCTCCCCTG | 1130 |
rs186560306 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235713333 | ACAAAAAAACTAAAA[C/G]AAAAATTAAGGTAAT | 1130 |
rs186572088 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235682317 | GCAAAAGGGCAAGAC[C/T]CTGTATGCCCAAGAA | 1130 |
rs186590927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235735542 | ATGCTGTAGATATTA[C/T]ACCTGATTCTACTGT | 1130 |
rs186663341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778725 | CAATCAGACATACCA[C/T]CCAGCGTATCTGTGC | 1130 |
rs186687443 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235841006 | CACAAGAAGAACTGA[C/G]GCACGTGTGCAGAGT | 1130 |
rs186702723 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235817129 | AAAAAATGCTCAACA[C/T]CACTACCAATTAGAG | 1130 |
rs186706033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235858348 | TGGAAAATATTTACT[A/G]TAGTGACTACTACAC | 1130 |
rs186708281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235850723 | GGCTAAGGACATGAA[C/T]AGACAGTTCTCAAAA | 1130 |
rs186727128 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235808127 | TTTCTCAGTTGTATA[A/T]CTAAAACTTTTCTTT | 1130 |
rs186741362 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738826 | ACCCAATTTCCACCA[C/T]GATTGGTGGAATAAA | 1130 |
rs186743134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235843699 | AAAAAAATAGGAAGT[C/T]CCTGTATTTTCTGCT | 1130 |
rs186745233 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235745802 | AGGCTACATACTGTA[C/T]GCTTCCATTTATATA | 1130 |
rs186746638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710654 | CCAGAATCTTGCTAC[C/T]CTCCATCACAAGGCA | 1130 |
rs186751863 | snp | C/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680503 | TTGGCTTCAAGTGGT[C/G/T]GTCCCACCTGGGAAG | 1130 |
rs186752856 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | LYST | GRCh38.p7 | 1:235879828 | TGCAACCTCTGCCTC[A/C]CGGTTTCAAGTCATT | 1130 |
rs186755053 | snp | C/T | 0.00014904 | 0.00863121 | intron-variant | LYST | GRCh38.p7 | 1:235716692 | TCATTTAATAAAGTA[C/T]GAGTAAAAACAAAAG | 1130 |
rs186756681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235767690 | ATTCTGTTTCTGTCT[G/T]TGCTTTTGCTGCTGG | 1130 |
rs186760726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235726443 | CATTCATTCAACATA[C/T]ATTAATTAACATCTA | 1130 |
rs186777847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786294 | AACTCTGACAGATTT[G/T]TAAGTTAAAGTATAG | 1130 |
rs186787548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822367 | CAGGACTGCTATGGC[C/T]GAGAGATGGCTATGT | 1130 |
rs186787739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737935 | TGGATCTCACTGCCG[C/T]GTGCCCCAACACCCG | 1130 |
rs186790436 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235805252 | TTTTAGGAGAAGTCT[C/T]GTCCCAGCCTCATTT | 1130 |
rs186846479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814740 | GGACATTCAGACTAC[G/T]CCTTCTGGTGTCCTG | 1130 |
rs186860146 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235795729 | TCACAATATTAGAGG[A/T]AATCTCCAACAGTTT | 1130 |
rs186862096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235830653 | AAATACCTGAGCATA[A/G]CTGAGAATAGGTAAG | 1130 |
rs186869652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668745 | TATAAACAATCATTA[C/T]ATTATTTCCCCAGTA | 1130 |
rs186924894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235788919 | AGTGAATTTAGAAGA[A/C]TACAAAGCAAATTTG | 1130 |
rs186934918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824841 | CCTGGCCAAGATGGT[A/G]AAACCCCGTCTCTAC | 1130 |
rs186947988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837203 | AGTCAATGGAGAGGG[A/T]AAGTATCCAACACAG | 1130 |
rs186948157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235880986 | AAAAAATTAGCCGGG[C/T]GTGGTGGAGGGTGCA | 1130 |
rs186960676 | snp | C/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861181 | TTAAAATAGTGAAAA[C/G/T]CTCTCTTATGTCCTC | 1130 |
rs187008071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851271 | ACCTGGATGAGACTG[A/G]AGACTATTATTCTAA | 1130 |
rs187023352 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235845722 | CTGCTGGCTTTCCCC[A/C]ACTTCCCTGACAACC | 1130 |
rs187025136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863287 | GTCCCAGCTACTCTG[C/G]AGGCTGAGGCAGGAG | 1130 |
rs187029299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706527 | CCACGTGAAGCCTCC[A/C]GTGCCACATAAAACT | 1130 |
rs187030069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882347 | GTGATGAAGCTGCAA[C/T]GGCAGAGGGAGCCGA | 1130 |
rs187045262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692258 | GAATTGCTTGAATCC[A/G]GGAGGCGGAGGTTGC | 1130 |
rs187049242 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235788488 | CCACCACACCCAGCC[A/G]AGAATTAATATATTT | 1130 |
rs187057848 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235687543 | GATAAATGTGAATGT[A/G]AAAGATGGGATTATG | 1130 |
rs187058895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748305 | GGGTGATGTGTAAAG[C/T]TTTTCATACTAATAA | 1130 |
rs187065454 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235774286 | ATTAGGCTTTAAAAC[A/G]TTTTCAAAAAAGTAG | 1130 |
rs187067340 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235725439 | ACTCTGTCTTAAAAA[A/G]ATAAAAAATAACAAA | 1130 |
rs187072542 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235793832 | TTTCTTTTTATTATT[A/T]TTATTATTATTATTA | 1130 |
rs187084474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811452 | TTTAAATAATTCTTT[A/G]TTCAAATTATTTCTC | 1130 |
rs187097098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674480 | CAAAGTTCCACAAGA[A/G]GTGCTAAATGAATTT | 1130 |
rs187101020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827853 | TCTATTTACCATATA[C/T]ACAAAGAAAATACCG | 1130 |
rs187123341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688686 | CTCAGAGCGTGAGTC[C/T]TTATATAACAAAATC | 1130 |
rs187125009 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235708719 | AGGCTGAGTATGCTT[A/T]TTGTGCTTTACCAGG | 1130 |
rs187210702 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235834159 | AATTTCATATCTTTA[C/T]TGAAGTTTTTAAATG | 1130 |
rs187219706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235870438 | CACTTCCATTTTCTG[C/T]ATGTCACTTTCCTTT | 1130 |
rs187236230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235770870 | GACAGTGCCTTAAAA[C/T]GCTTCTCCCATATTG | 1130 |
rs187257944 | snp | A/T | 0.000131835 | 0.00811788 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806656 | TTCTGTTGCTCCCCT[A/T]GGCTGATTATCAGAG | 1130 |
rs187264404 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235704101 | TTGTTCTTTTTTATG[G/T]CTGCAAAGTATTCCA | 1130 |
rs187267333 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235722316 | TCTGAGCAGAGAAAA[G/T]ATATGATCCAACATA | 1130 |
rs187280206 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235689688 | GCTAACTATGTGAGG[C/T]GACGAATGTGTTAAT | 1130 |
rs187296884 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235729430 | ATCATTTCTTCACAT[G/T]CATGACTCATATGCA | 1130 |
rs187297003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669276 | TCATGCCCACCTCCT[A/G]GTGAGGCAGGAGAAT | 1130 |
rs187303003 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866293 | AAGGGTGTCACGGAC[A/T]GGAGGAAAGAGCGGA | 1130 |
rs187308285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740063 | CCATTTCAAATTCTC[C/T]ACAGAAGGAAAATAC | 1130 |
rs187314331 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235766605 | TTCTCCACTCACTAG[C/G]CATGTGATCTTAGGT | 1130 |
rs187325680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235733100 | GTATTTTAGTACACC[A/G]AAGTCACATGAATAA | 1130 |
rs187333633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235670999 | ATATTGGAAAGATAA[C/T]GAAAAGACAGTAAAC | 1130 |
rs187337798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235694958 | AAGCTTGGACTCAAG[C/T]CCCAGAGATTCTGAT | 1130 |
rs187342486 | snp | A/G | 0.000333806 | 0.0129148 | intron-variant | LYST | GRCh38.p7 | 1:235697066 | TCCAGAATGATCTTC[A/G]TTACATTTTATTTTA | 1130 |
rs187346920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235711697 | ATAATTGAGATTTCA[G/T]TTAATTTACATTTTG | 1130 |
rs187349892 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235803623 | ATTTTCCTTTTCTTA[C/T]AAAAATTCCACTAAT | 1130 |
rs187357084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749808 | TAAACTTGAAGTTAC[A/G]TAGGGCTCTAAGGCT | 1130 |
rs187360364 | snp | A/G | 5.53337e-05 | 0.00525964 | intron-variant | LYST | GRCh38.p7 | 1:235791605 | GAAGAACATGTTAAG[A/G]GTGTTAAGAACACTA | 1130 |
rs187363749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773578 | TATACGATCCTACTT[A/G]TATGAGATCCTTAGA | 1130 |
rs187410791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724319 | ATTACCTGAAAACTC[C/T]CCCAATGCAAAACAC | 1130 |
rs187421974 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235691494 | AGATGGCACTATGGT[C/T]ACAGAAAATGACCTA | 1130 |
rs187470590 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235848559 | ATTGAAACAAACAAA[A/C]AAAATACAAAAGATA | 1130 |
rs187508290 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867213 | GGGTCCGCACCTCCT[C/G]CCAGGGCTCTGCGTA | 1130 |
rs187509831 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235848933 | ACGGCAGAATTCTAC[C/T]AGACATTTAAAGAAT | 1130 |
rs187519435 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885302 | ACTAACTAGACTGTT[A/C]TTTGCATGTGTGTTA | 1130 |
rs187538660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235815644 | CATACATCGACAACA[C/T]CCAAGCTGAGGGGCA | 1130 |
rs187540043 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235849357 | AAATCGGCATACAAG[A/G]GTCATACCTTAATGT | 1130 |
rs187541735 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235876681 | CTGTTTGTTAGTAAA[G/T]TTCTGTTTTCTGCAA | 1130 |
rs187568359 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884846 | AGCCCAGGCCAGAGC[A/G]CAGTTGTGTGACCTT | 1130 |
rs187586955 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235778051 | CCTCAGCCTCCCAAG[C/T]AGCTAGGACTACAGG | 1130 |
rs187590373 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235784867 | ATGGCAGCTATGAAG[A/C]TCGAGAACGTCACAG | 1130 |
rs187590438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235743168 | TTCCCTAACAATTAA[C/T]CAATTGTTTTAACTA | 1130 |
rs187603372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235696338 | AGAAGGTAATGGTAA[C/T]TGCCAGCAGTGCTGG | 1130 |
rs187616334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235680888 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCTACAA | 1130 |
rs187622132 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706946 | TCAGATATGGAGTGG[C/T]CTACTGTAGGTTCTG | 1130 |
rs187622686 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662298 | TTGTGGCTGTCAAAA[A/G]AATTCTGGTTCTCCT | 1130 |
rs187630063 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235674173 | CTCTCACGACAGGGG[G/T]AATATTTGGCATTCC | 1130 |
rs187636459 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676104 | GATGCATTGGTTTCT[C/T]AACATGTATATATGA | 1130 |
rs187659903 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235706195 | AGTTTAGGACACACA[A/G]CCCCAAAATTTCGTA | 1130 |
rs187695446 | snp | C/T | 0.000483208 | 0.0155361 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762702 | AGAAGGTCATACTTC[C/T]ATTATTGCTATTTTT | 1130 |
rs187700720 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235722431 | TGGAGGTCAAGAAAG[C/G]GTTTGTCAAAGTCAT | 1130 |
rs187711343 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740545 | TTTGGCTGTCCCTTT[C/T]CCCACTCAATGTTTC | 1130 |
rs187717790 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235781493 | TAAGGACATATTTTT[A/T]AAAAATCATATATTT | 1130 |
rs187730676 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819629 | TCAGCCAATAACATA[C/T]CACTCTTATTTAATA | 1130 |
rs187730847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862573 | GGCCAAGATGGGCAG[A/G]TCACTTGAGGTCAGC | 1130 |
rs187733808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802078 | GGGCTCCTGAAATCC[C/T]AGCTACTTGGGAGGC | 1130 |
rs187733831 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235845430 | GTAAAACCCCACAGG[G/T]AAAGGAATTCTCTAG | 1130 |
rs187752762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853221 | AAAATGTTGCTCCTC[C/T]TGAAAAGAAGTATGT | 1130 |
rs187772450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796587 | TTGCCATTGTGGTAG[C/T]GTTAAGAGATGGGAT | 1130 |
rs187783952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235831356 | CACAAGATGTGACTC[A/G]TATAGTGTGGGTTGC | 1130 |
rs187803328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755708 | ATATAATATATACAA[A/T]TCAGTGTAACACAAC | 1130 |
rs187806508 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867684 | CTGGGCCCAGCACGC[C/T]GCTGGCAGACTGCTG | 1130 |
rs187814471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814415 | AATGACAATAGAAGA[C/G]CATCAAGAATGAAAC | 1130 |
rs187837317 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235685666 | GTCTGACCAACATGG[C/T]GAAACCCTGTCTCTA | 1130 |
rs187843528 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235757048 | GGAGGGGGACTTAAA[A/G]CTGGATGATGCAAAA | 1130 |
rs187858237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715869 | GCAGTTATCAGAGAT[A/T]AAAAAAAAAAAGAAT | 1130 |
rs187861796 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235737459 | GAGAAATAAACATAC[C/T]TAGTCCTTAGATTTG | 1130 |
rs187871628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235699697 | TACATTCCCACTAAC[A/G]GTGTAAAAGCGTTCC | 1130 |
rs187871755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235676514 | TCCTTCTGCTTTAAT[C/T]CTCTAAGGAAAGTAA | 1130 |
rs187875730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235715448 | TTTTCTCTCCTTCTC[C/T]ACTACCCCTTTGAGG | 1130 |
rs187896665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235755414 | AAAAGAAAAGAAAAG[A/G]AAAGAAAAGAAAAGA | 1130 |
rs187896876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235795531 | CTATATGTGAAAGAT[A/G]CATTTTTCTAAGGTA | 1130 |
rs187897928 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235692791 | TCTGGGAGGCCAAGG[C/T]GGGTGAATCATTTGA | 1130 |
rs187898207 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235877171 | TGCTATCCATATAAC[C/T]GAGTGGTTGTACCAG | 1130 |
rs187904837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776560 | TCCCTGAAATAGTCT[A/G]TAATTACTGACTGTC | 1130 |
rs187929073 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235685023 | CATTCTTCCCCAACA[C/T]GTTACACTCTAAACT | 1130 |
rs187986839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841572 | GCCACTTTACTAGCA[C/T]ACCACTGCAGCCAGC | 1130 |
rs187988975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235858705 | ACCACTCTCTATTCC[C/T]TGACTTCCCACTACC | 1130 |
rs188013645 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235860038 | CACTTGGCAAGCTGG[C/T]CTATAGTTTTTCTAG | 1130 |
rs188020814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878957 | TGAGTAGTGGTGAGG[A/T]CTGGGCTGTTAGAGT | 1130 |
rs188034454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872399 | TTCTGCTTAGATTCA[A/G]TGAAGAATGGACAGC | 1130 |
rs188034895 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801422 | ACTTTCTGACCCCCC[C/G/T]CTCAAATACCTAAAT | 1130 |
rs188068794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871808 | GAATCTGCTCTCAGG[A/G]TCTGGGACAAGATCC | 1130 |
rs188070823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235787751 | GTATTGGAGGTCTAA[C/T]CTACTTTGTGGGATT | 1130 |
rs188078525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737694 | TTTAATATCAAACTG[A/C]ATAATGACTGCAATA | 1130 |
rs188084270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235777580 | TTAGAATATATATTA[A/G]GTTATACTATTACTA | 1130 |
rs188095579 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235842286 | AATCAAGGAAGTGTG[G/T]ATCTCTACCAGACTG | 1130 |
rs188099623 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235823870 | GTCATCATTTATTTA[C/T]CTATCTCTTCAAAAG | 1130 |
rs188108477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235762191 | ATTGTACAGTATTTG[A/G]AAATGTTTCAGAGTG | 1130 |
rs188121583 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235666758 | ATATTTTCCATGAGT[A/G]GGCTACATTTCAACC | 1130 |
rs188132960 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662067 | TATTTAGGCTGTGTT[C/G]TTAATACCCATGCAA | 1130 |
rs188161811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235699990 | CAAGCAATGGGGAAA[A/G]GATTCCCTATTTAAT | 1130 |
rs188243628 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235700457 | ATAGAATATTTAAAG[A/G]GGAGTGCTTTATTGA | 1130 |
rs188253070 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235855771 | ACTGAACACAGATAT[G/T]TATAAGCTTTAAATA | 1130 |
rs188260768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686367 | GGGAGGTTCTGTCTC[A/G]AAAAACAAAAACAAA | 1130 |
rs188289854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235810738 | TAAACACTAGCTGAC[A/G]TTAGTTCAAAGGATA | 1130 |
rs188292136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235845584 | TGAGAGGTGGATAGC[C/T]TCGGGGAAGTTTTCA | 1130 |
rs188312797 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235667659 | ACCTCTGCACATCCT[C/T]CTGTATTCTTTTTTT | 1130 |
rs188314365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742855 | TTCCACAGTCAACCA[C/T]GGTCTGAAAATAGTT | 1130 |
rs188319753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235881629 | TATATCACTGTGTGT[A/G]TGTATATATATTTAC | 1130 |
rs188320362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235784425 | AAAAATCTAATCTCT[A/C]ATTCTGAACATTTCT | 1130 |
rs188323935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235765768 | TCTCTCCACAGTGGT[C/T]GGATGAAACCCTCTG | 1130 |
rs188324954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235781215 | CGAAATTGGTGTAAC[A/G]AGAAAATAACCTATG | 1130 |
rs188328426 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235821040 | TCCCACATTTAGCTT[A/T]CATATTCCACTTTAC | 1130 |
rs188334881 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235819520 | TGTTCCCTCATGACA[A/T]CCAAGTGGGAAGTTC | 1130 |
rs188336491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803449 | TAAAAAAGATTTTTT[C/T]ATAAGGATTTTTATA | 1130 |
rs188340585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839348 | TGCAACCTCCACCTC[C/T]CAGGTTCAAGTTGGC | 1130 |
rs188340861 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852704 | AAACTGCCAGAGTTC[A/G]CATTTAATAAATTAT | 1130 |
rs188341754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739317 | CTGCACATGCTGCAG[G/T]TGGCCCTTGAGCCAG | 1130 |
rs188342673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235863746 | GGTGAAATTTTTAAC[A/C]CCCTGGTATAGTCAA | 1130 |
rs188343983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882771 | GTCCATGTTGGAGAT[A/G]TTCAGTTTCATGTGC | 1130 |
rs188346548 | snp | A/T | 0.134802 | 0.221877 | intron-variant | LYST | GRCh38.p7 | 1:235780417 | TCTTAAAAAAAAAAA[A/T]AAAAAATAAAAAAGA | 1130 |
rs188350143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235726947 | TGATAAAAGGATCCA[C/T]CTTGAAAAATAACAT | 1130 |
rs188374983 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235707823 | TATAGGTTGAGTATC[A/C]CTTATACAAACATTT | 1130 |
rs188386169 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235669873 | AGAACCTGGACAACT[C/T]GCAGTCAACACCCTC | 1130 |
rs188395576 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235769520 | TGTACTTATCTAACT[A/T]GACAAAGTTCTAATC | 1130 |
rs188395674 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYST | GRCh38.p7 | 1:235786882 | GGAAGGGAAACATCA[C/T]ACACTGGGGCCTGTC | 1130 |
rs188422203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235702611 | CAGGATTCTGCTTTC[A/G]CTGCTGCACCTGTCT | 1130 |
rs188432281 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235694220 | GGGTTTCATCATGTT[A/G]GCCAGGCTGGTCTCG | 1130 |
rs188432449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677432 | TTCATATAGTAAAAA[C/T]GGATATATTAAAAAT | 1130 |
rs188554628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859160 | CATTTCCTTTTCGTT[C/T]TTAAACAGGAAGATA | 1130 |
rs188566639 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827758 | TACCACCACAGGAAA[A/G]AAATATTTAACTTAT | 1130 |
rs188588555 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235862990 | TAAGCTAAATTTGTT[A/G]TAATTTTGTCTTTTG | 1130 |
rs188599380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723704 | CAAGCATATGCAACT[C/T]TCCCCAACAGTTTTT | 1130 |
rs188599890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791174 | TGAATCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 1130 |
rs188604129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827046 | ATACCTCAATAAAAA[G/T]TTTATTTACTTCTTT | 1130 |
rs188605749 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235742221 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 1130 |
rs188635193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235760067 | AATGGTTCTACTGTG[C/T]TGAATTTAAGTGAAT | 1130 |
rs188635826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764685 | TTTTTTTATTTTTAG[C/T]AGAGATGGGGTTTTG | 1130 |
rs188638318 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883573 | CCAAAACCCCAAACA[C/T]TCTGGTATGAGGACT | 1130 |
rs188663695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749501 | GATGTGGTGCAGGAC[A/C]CAAAGGGGTGAGTAT | 1130 |
rs188664078 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235711067 | GAACTTCTGACCAAT[A/T]TCTTATTTCTGACCA | 1130 |
rs188669352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690451 | ACTTGTTTGTGTTTG[G/T]ATATATATATTTCTA | 1130 |
rs188670943 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235691183 | TCGGCCTCCCAAAGC[A/C/G]CTGGGATAACAGGCT | 1130 |
rs188685773 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235673665 | TGCTTCTATGGTCTA[C/G]GAGAAAATGCCGTTA | 1130 |
rs188694418 | snp | C/T | 5.03622e-05 | 0.00501782 | intron-variant | LYST | GRCh38.p7 | 1:235720954 | TTATTTTTAGTCTTA[C/T]TGGCACTTTTCTCCA | 1130 |
rs188696852 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662611 | GTCCTTTTGGAATCA[C/T]AGAAAAAGGGGAGAC | 1130 |
rs188831395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842036 | ATTTTTTCAGCTATT[A/T]CAGATTCACCAGCAG | 1130 |
rs188839448 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235877836 | GATCTATTCGGAAGT[A/G]TCTGACAATATCTGC | 1130 |
rs188842161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235768234 | TTGTTTTTCTGGTCT[C/T]CCGGCTTGAAATTTT | 1130 |
rs188844231 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235805563 | TGTGTATGTGTATAT[A/G]TACATAAAACATAAT | 1130 |
rs188844339 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235829965 | ACCATAGTTATCTCA[C/T]TGATATTACGATAAA | 1130 |
rs188870379 | snp | C/T | 0.00013187 | 0.00811895 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810366 | CTTACAGAATAGCGA[C/T]GGGTAATTTTACGCT | 1130 |
rs188874588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772828 | TCAGCTGATCCAGAT[A/G]AGCCCATATGCTCCT | 1130 |
rs188875077 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235693629 | TAAATCTCTAAAATG[G/T]AACAATTTTTTAGTT | 1130 |
rs188904941 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235672801 | ATATCGGCTTATCCC[C/T]GTATAAAATGCTTTA | 1130 |
rs188921370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726554 | CATTTGCACACACAA[C/T]GCAAGATACCAAATG | 1130 |
rs188926409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872831 | TTAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 1130 |
rs188933222 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235731838 | GTTGGGATTACAGGC[A/G]TGAGCGCCCTCACCT | 1130 |
rs188943814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235704512 | TATTGATCAGTGATA[C/T]TGAGCTTTTTTTCAT | 1130 |
rs188950214 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672645 | GTAGAACTTTCCATT[A/G]TGAAAAGGGATTTGA | 1130 |
rs188967571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235666450 | AGAGGTTACCAGGGG[C/T]TGGAAGCTGAGGGAG | 1130 |
rs188978101 | snp | C/G | 0.000484573 | 0.015558 | intron-variant | LYST | GRCh38.p7 | 1:235753297 | AAATAATACAGTTAA[C/G]AGCACATTAGAAACA | 1130 |
rs188994927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235735945 | GTACATGACTAAAAG[A/G]CTTTCCTAAGTGTGT | 1130 |
rs189002463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838082 | GAATACGAGTATAGA[C/T]GTAGGAAGATTAGTA | 1130 |
rs189002638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794969 | AGAAGGAAGAAATCC[A/G]TAACAGCAAAAATAT | 1130 |
rs189006549 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235819688 | GTCTCACTCTGCCAC[C/T]CAGCTGGAGTGCAGT | 1130 |
rs189010317 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235775281 | TCCATGTTCTATAGT[A/C]TCTTATATATACTAT | 1130 |
rs189010532 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854080 | TACACTGACTACTAC[A/G]TCCCTCCTCAAAAGA | 1130 |
rs189018382 | snp | A/T | 1.77335e-05 | 0.00297765 | intron-variant | LYST | GRCh38.p7 | 1:235813072 | AATGCCTATGTCAGT[A/T]ACAAAAGAATCCTTC | 1130 |
rs189034300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235817279 | CAACGCTGGTGGGAA[C/T]GTAAGTTAGTTCAGC | 1130 |
rs189038437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235850746 | TCTCAAAAGAAGATA[C/T]ATAAATGGCCAACAA | 1130 |
rs189051194 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | LYST | GRCh38.p7 | 1:235698637 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 1130 |
rs189057155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713401 | AAGACTAAGGAAATA[C/T]GGAACAAGAGTAGCA | 1130 |
rs189106299 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235786691 | TAAGAAAATGTGGCA[A/C]ATATACACCATGGAA | 1130 |
rs189122857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678022 | ACTATCCTTCATTGA[C/T]AGACACTTAAAATTG | 1130 |
rs189142645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235822705 | TTAATTGCAGTTCCT[C/T]CTATCAAGTGATAGA | 1130 |
rs189166845 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235708456 | CTTGGCTGTTGTCTG[A/G]GAACCTGGATTTCAG | 1130 |
rs189174982 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235869340 | AGCCGGGCGCGGTGG[C/T]GGACGCCTGTAGTCT | 1130 |
rs189190711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746150 | GTCTGGGCTAGCATC[A/G]AACACATTCAAAGTG | 1130 |
rs189197039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707486 | AAATTAGCCAGGTGC[A/G]GTGGTGGGCGCCTGT | 1130 |
rs189235195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235816316 | CATGATGCCATGTGC[C/T]TGTAGTCCCAGCTAC | 1130 |
rs189245331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235833385 | TTTGCTTTTTCCTCT[C/T]AATGTTATGTTCATT | 1130 |
rs189268458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850244 | ACAGCCAACTGATCT[A/T]TGACAAAGCAAACAA | 1130 |
rs189280618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713086 | TTCTCCCAGCCTTAG[G/T]TGCTCTGCTGAGCAA | 1130 |
rs189288908 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235682206 | GCCCCAGCTATTGGT[A/G]GGGGGTCGGGGATGG | 1130 |
rs189290722 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235697999 | AGGTTTCCTCCACTT[C/T]AAGCAAAAACAGTTA | 1130 |
rs189328742 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235833950 | AAGTTAACTGCAAAG[A/G]AGAATTAGACCAGTC | 1130 |
rs189332078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794442 | ACAAATTCATAGAAT[C/T]CTTTGGAGCAAAATA | 1130 |
rs189336890 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828112 | GCTAACACTACAGAC[C/T]AGCAAAATATTCCCA | 1130 |
rs189353857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235663766 | CATGCCTTTCCACTA[C/G]ACTCTGAGTCACTGA | 1130 |
rs189355255 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235860323 | CTGGTACATTTGTTA[C/T]AATCAATGAACCTAC | 1130 |
rs189370135 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235879776 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 1130 |
rs189379883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235687568 | ATTATGCCTTTGGTA[C/T]AAAATCCCTCAGTCC | 1130 |
rs189408064 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758184 | ATATAAAGTTATGGG[C/T]CTGCGATAGCAGAAG | 1130 |
rs189411800 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235718750 | GGTTACTCTAAAATA[A/C/T]AGTTCATTCAGGAAA | 1130 |
rs189443497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729065 | CCTACAGCATACAGA[C/T]TGATTCTTTAAGGGA | 1130 |
rs189447167 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235694737 | AGGAACCACATATCA[G/T]GAGTCTTGAGTCCTC | 1130 |
rs189478379 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235832634 | ATACTGCTACATGTA[A/G]ATATTACATATATAG | 1130 |
rs189520280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757762 | AGTTGCATCAGCCAC[A/T]TTTCAAGTGCTCAGT | 1130 |
rs189530187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235717350 | GAGTAATACCATTGC[A/G]CACAGTGTAGAGTAT | 1130 |
rs189538066 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235695112 | TGTAGTAAACACTGA[C/T]CTCTCCCAGACCCTA | 1130 |
rs189538414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738199 | TGATGGATCTCCACC[A/G]TGGCAGCCTTTTCCT | 1130 |
rs189542268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797735 | GATTTCTTAGATATG[A/C]CACCAAAGGTACAGC | 1130 |
rs189548067 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235778141 | TGTAGAGACATGGTC[C/T]TGTTATGTTGCCCAG | 1130 |
rs189555909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815931 | AGGTCAAGAGATCGA[C/G]ACCATCCCGGCCAAC | 1130 |
rs189574422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874386 | CAAGCAACTATAGTC[A/G]AGGGAGATGAAGGTT | 1130 |
rs189588723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701256 | AACTTTAACAGCTAA[C/T]GAGCAGTAAGTATAG | 1130 |
rs189594655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235838570 | GTGGAAGTAACATCA[A/G]GTTTACAAAAATCTA | 1130 |
rs189607199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235873639 | GGGTCTATTATTGAG[C/T]ATAATTCTTAGCCAG | 1130 |
rs189624911 | snp | A/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738906 | TCAGACCGTGTGAAG[A/G]TGACTCTGACTCCTG | 1130 |
rs189629359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235811934 | CAGAAAAACAGTATT[A/G]CAAAACCTTAGATAC | 1130 |
rs189631934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235701889 | TATGTGAGCTATGAG[C/T]GCAAATAATTTATAT | 1130 |
rs189635944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719005 | AGGCACTTCAAGTTG[C/G]CTTCTGAGTCCTTTT | 1130 |
rs189642441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846503 | TCTAGTTCACCAGCA[A/G]TAGATCCAAACCAAG | 1130 |
rs189653302 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235880635 | CAAGAGTATTTTTTC[G/T]ATTCTTGGTTCAGGG | 1130 |
rs189657766 | snp | C/T | 0.000198672 | 0.00996477 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759020 | TCATAACCAAGAGAA[C/T]AGGCAAAGTTTTCCC | 1130 |
rs189663211 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | LYST | GRCh38.p7 | 1:235701552 | AGAACTGTTTGAACC[C/T]GGGAGGCAGAGGTTG | 1130 |
rs189670918 | snp | C/T | 0.000704686 | 0.0187576 | intron-variant | LYST | GRCh38.p7 | 1:235803099 | AAAGGTTGTAACATT[C/T]GCTTGTTTTTAGTAA | 1130 |
rs189675898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668919 | GTTTTCATGACATTA[G/T]TTTACAACTGGGGGC | 1130 |
rs189679893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738782 | GGCAGATTTGGCAGA[A/G]AGTATAATGAAGAAT | 1130 |
rs189699606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235688519 | GGCTTTCATTGAACA[C/T]GGTGGAGAATTCAGA | 1130 |
rs189700601 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662693 | TTTTAATGTACCATG[A/C]GAGGCTTAAAACTTG | 1130 |
rs189702409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235790587 | ACTGGATGAGAAAGA[C/T]TTGTGGAATGAAGAG | 1130 |
rs189702994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669044 | ACAACAATAACAAAA[C/G]CCTAACAGGTATCTG | 1130 |
rs189717590 | snp | A/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809545 | TGGCTTGACTGAAGT[A/T]GAAGGGATTTGAAGC | 1130 |
rs189728307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235733429 | GAGTCTGAATTCCGG[A/C]ATACAAATTCCGTTT | 1130 |
rs189729967 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697639 | TATGACAAGCCATAT[A/G]TACATATGGTAATAG | 1130 |
rs189731173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844704 | TCTCTACAAACTTTT[C/T]AGACTACAACACAGA | 1130 |
rs189735113 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826854 | ACCTGGCTAATTTTT[C/G]TATTTTTTTGTAGAG | 1130 |
rs189745527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235862390 | AGAAATAATTCATAA[C/T]TTCAAATTGCACCCT | 1130 |
rs189843359 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847059 | TCAAAAAGATCTTCG[C/T]GTAGGCACATTGTCA | 1130 |
rs189847755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820022 | AATTCCCCATAGAAA[A/C]AACAAACAGTAAAGT | 1130 |
rs189864115 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854577 | TGACCTTGGGTACTC[A/G]ACTTCCTCTTTCTAA | 1130 |
rs189866008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737270 | TATGTAGAAAGACAA[A/G]GCAAATAAGTGATTA | 1130 |
rs189869537 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883311 | AGCAAGCTGGGTCTC[G/T]TGTTTGCAGTTAGAT | 1130 |
rs189885843 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714851 | CTCCAAAGGTAACTT[A/G]CTGGATTTGAAATAA | 1130 |
rs189892575 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235782247 | GATCTCAGCTCACTG[C/T]AAGCTCCGCCTCCTG | 1130 |
rs189902086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235876736 | ACATAATCATTTGCC[C/T]AGCTCACTACATAAG | 1130 |
rs189916184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750539 | GGAGATGGTGTGTGT[C/G]TGTGCATGTGTACAT | 1130 |
rs189942674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235704990 | TAAGGGCAACAGGCA[C/T]CTCTACATGCCTTTT | 1130 |
rs189943445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235782716 | ATAAACCAACCACCT[C/G]CCCTTAATTTTGCCA | 1130 |
rs189947436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235681937 | CAGCTGTGACACGTT[A/G]GGCAAGTTACAAGAA | 1130 |
rs189965982 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235741177 | ACATTACAAAGTTTC[G/T]GACAGAAACTCTGAA | 1130 |
rs189975523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712695 | TCTTTCTTTTTTTTC[A/G]GGGGGGTGCGTAGGT | 1130 |
rs189976126 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235841026 | GTGTGCAGAGTCTGC[C/T]GTCAGGGCAAAACCA | 1130 |
rs189976474 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235682318 | CAAAAGGGCAAGACC[C/T]TGTATGCCCAAGAAG | 1130 |
rs189996514 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858557 | ACTCTTTTATTTCCA[C/T]TAATCCTGCACTTGA | 1130 |
rs190072829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669901 | CTCTACCAGTGACAC[C/T]GGGAGCAGAGTGGGG | 1130 |
rs190076893 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235695685 | TCTCCCAGGCTGGAG[C/T]GCAATGGTGCGATCT | 1130 |
rs190082819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710244 | AAATCAAGGGTTTAT[A/G]TAAATTCACATGGGA | 1130 |
rs190092643 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235680094 | TTATATTAAAATATA[C/T]ACTTATAAGTTATAT | 1130 |
rs190103153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828671 | CCTCGATATTTACTA[C/T]TACTGATGCTATTTA | 1130 |
rs190117248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235863992 | TGATCAGGTTCCTCA[C/T]CCTCCACCATTCCCC | 1130 |
rs190144087 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235823175 | TAATTAAAACGGGAA[C/T]AATTCAATGAATTAT | 1130 |
rs190154203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763930 | CTCTCTCTCGAATGT[C/T]AACTCCTGCTTAAAA | 1130 |
rs190158396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798889 | GGGTTTCTTTTGGGG[G/T]TGATGAAAATGTTCT | 1130 |
rs190163446 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802364 | ATCATAGGCAATATA[C/G]TTCCATCCTAAAGAC | 1130 |
rs190195959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235664943 | GGACAACAGGTGCAC[C/G]CCACCACATCCGGCT | 1130 |
rs190200108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235691139 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 1130 |
rs190238939 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235723056 | TATTCTGAGGACAGA[C/G]CCAACAGAACCTATT | 1130 |
rs190251672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767492 | TTCTGCTACAACCAT[C/G]TGCATTTCTTCTAAA | 1130 |
rs190257717 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235813261 | TCTAATGATAGAAGA[A/G]TCTAAGAGTATTTGA | 1130 |
rs190263699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235725884 | CACATTCTGAAATGA[A/G]GAGGTAGGGACCACA | 1130 |
rs190266074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235744376 | TGTCATACAATTCCA[A/G]ATTAAATATTTAATG | 1130 |
rs190268158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235795125 | GCAGTAAGAAGCCGA[A/G]CTGTCCATCTAAGGT | 1130 |
rs190280065 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235829484 | TTTTTTCAACTAACT[A/G]TATTAATTAGTTCCC | 1130 |
rs190290495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847984 | GGTCATCAACACAGA[A/G]GGTCAACAAAGAAAC | 1130 |
rs190330362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235706661 | GAAGGCATTTTTTCT[C/T]CCTTACATATTAATA | 1130 |
rs190336308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235692527 | CTGGAATTACAGGAA[C/T]GTGCCACCATGCCTG | 1130 |
rs190340684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674805 | ACAAAAGCCCTACAG[A/G]GCCTTACCACCCTAG | 1130 |
rs190366791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235795532 | TATATGTGAAAGATG[A/C]ATTTTTCTAAGGTAT | 1130 |
rs190370406 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235755423 | GAAAAGAAAAGAAAA[C/G]AAAAGAAAAAAGACA | 1130 |
rs190374209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776599 | ATCAGGACAGATAAT[G/T]AAATGACTCATTCGA | 1130 |
rs190380326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814452 | CTTTAAAGACTTAAA[A/G]ATGGGCAATGCTAAA | 1130 |
rs190382605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840208 | CAATATATAGGGTAC[C/T]ATGTACTGCTAAGGG | 1130 |
rs190386164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807754 | GGAAAACTCACTGAT[A/G]GGATTAAAAGTAATT | 1130 |
rs190386299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857247 | TAACCAGAGAAGCTA[C/T]CACCTTAGAAATGGT | 1130 |
rs190388673 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235875412 | ATATCTTGGGGCTAT[A/T]GTGTGGCAATTACAG | 1130 |
rs190393655 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235778423 | TCTGTTGCCCAGGCT[A/G]GAGTACAGTGGCGTG | 1130 |
rs190397375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829994 | AAAAGCATAGTATAT[A/G]TGAAACCATTTAGTT | 1130 |
rs190397981 | snp | C/T | 6.6036e-05 | 0.00574575 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806071 | ATTCTGTTTAAATCC[C/T]GGTTTTCATTTACAC | 1130 |
rs190408896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235868975 | GCTGGGATTACAGGC[A/G]TGAGACACCGCTCCT | 1130 |
rs190419612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235842787 | TTCATTGAATGAGAC[C/T]TCCTGCAGACATCTG | 1130 |
rs190437079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737537 | GGGAGGGAAGTTAGG[C/T]TCTAGGTTTGGGGAA | 1130 |
rs190467814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774648 | GGGACAGCATGGGAG[A/G]TATCTATGGCCCACC | 1130 |
rs190474186 | snp | A/T | 1.64776e-05 | 0.00287028 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734541 | GGAGGGATGCACTTG[A/T]GACCACATAACTTCA | 1130 |
rs190477191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729498 | ACTACAGAAAGTTTA[C/T]CCAATTTAATGGCAT | 1130 |
rs190531106 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | LYST | GRCh38.p7 | 1:235668271 | GTCAAAATTTTTGAT[A/C]GGTTAAATCTGATAA | 1130 |
rs190613033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674197 | GCATTCCTTGGAAGC[C/T]TAACAGGACGCAGTG | 1130 |
rs190614119 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235834977 | TTGAGTGCAGTGGCG[C/T]GATCTCGGGTCACTG | 1130 |
rs190622027 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235851884 | TTCATGAAAACCAAT[G/T]TAACAATAATATAAA | 1130 |
rs190638400 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235871527 | CTTTAAAGATCATAT[A/C]ATATACTCATTAATT | 1130 |
rs190643006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235849801 | AAAAAAAAAAAAACT[C/T]AGGAAGACACCTAAC | 1130 |
rs190647059 | snp | C/T | 1.65512e-05 | 0.00287669 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788816 | TTTCACCAGGATTTA[C/T]GTACTCTGCACCTTC | 1130 |
rs190650928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824704 | ATTATGAACAAAATG[C/G]AGTTTATTCCAGGAA | 1130 |
rs190686721 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235708759 | TTGGATGTTTGTGCC[C/T]GCTTTCTCCCAGACT | 1130 |
rs190697968 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235680585 | GATATTTCTAATAAG[A/G]ACACACAAGTGATTT | 1130 |
rs190707719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235778952 | GCTCTCTGCAATCTC[C/T]GCCTCCTAGGTTCAA | 1130 |
rs190714241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749247 | TACTTTTGAAGATAC[A/T]TTTAAGTAATAGTGG | 1130 |
rs190723335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710741 | TAGGAAGAATACAGT[A/G]GAAGTGATGCTGCGT | 1130 |
rs190728010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699370 | GTGTTAGTTTGCTGA[A/G]GATGAGGGCTTCCAG | 1130 |
rs190730459 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235748576 | ATTTAGGTAAAATTA[C/T]ATATAAAGATATGTA | 1130 |
rs190737808 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235666082 | CATATAAACAATGCT[G/T]CTTTATTTAAAAATA | 1130 |
rs190775839 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235686735 | GATCTAACTCAAAAT[A/G]CCGTCTCTGAAAAAA | 1130 |
rs190787234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235749036 | CCTAAACATTTATCA[A/G]TAAAGAGAACGGCTT | 1130 |
rs190799864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235730289 | CTTAATACTCAACAA[C/T]GCTATGATACCTATT | 1130 |
rs190814927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235789821 | CCAAATATGAACTTC[C/T]GCAAATAAAAGAGTA | 1130 |
rs190835099 | snp | C/T | 0.000184565 | 0.00960461 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808433 | AACCCCCGCCCCCGC[C/T]GCCACCCACACACAT | 1130 |
rs190850203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235851448 | GACTACAAATATGGT[A/G]CAGTGTATACTGCTT | 1130 |
rs190881351 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235829750 | ACTTTAAGCCAAAAA[C/T]GTTTGATAAATTAGA | 1130 |
rs190900587 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772422 | ATCTAGTTTTTTTTT[G/T]GCAAAAATCATCAGT | 1130 |
rs190905623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866024 | AGCGGATCGGGGATG[A/T]TTTGCTATGTTTTGT | 1130 |
rs190911004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235780074 | GCAGAATTAGCAATA[C/T]TTTGAAAGCAAAATT | 1130 |
rs190922843 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235818106 | ATAATTAACTTTAAT[A/C]ATTTCATGATTATTT | 1130 |
rs190926422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799448 | AGTTAACATCACCAG[C/T]AGTAAGATCCAGATA | 1130 |
rs190934617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695845 | TTTCACCGTGTTAAC[A/C]AGGATGGTCTCGATC | 1130 |
rs190936124 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235834343 | CTTATCATAGTTATG[C/T]GGCAAACATGAAGAT | 1130 |
rs190956886 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662131 | TTGGTACAGATTCAA[C/T]GCTCTGTAAATAGCA | 1130 |
rs190967143 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235754827 | ACCTATAATCCCAAC[A/C]CTTTGGGAGGCCAAG | 1130 |
rs190973330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739135 | ATTCCTAAGGTTAGA[A/G]ATAGGAATGGTTTGT | 1130 |
rs190975027 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235799368 | GATACTTATTAATTA[C/T]AAAGGGAAAATAGTA | 1130 |
rs190975490 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235795462 | CTGTGATGCCTGGAT[C/T]AAGAAAGGGATGCCT | 1130 |
rs190980865 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661264 | AGTTATTCTGCATAT[C/T]TTCTCTTTAGATAAA | 1130 |
rs191019231 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235880987 | AAAAATTAGCCGGGC[A/G/T]TGGTGGAGGGTGCAT | 1130 |
rs191086684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811491 | CAGCACTGAACTAGG[C/T]ACCAGGTATAGACAC | 1130 |
rs191109276 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827904 | TGGTTCCAGAATACA[C/T]AAAGAACTGCTACAA | 1130 |
rs191119449 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846077 | AACCAGTACAAAAAT[A/T]GAGCATTAAACCACC | 1130 |
rs191135423 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235882517 | GATTGGAGGTGAAAG[C/G]GACTAGAGGCAGAGA | 1130 |
rs191139147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235814046 | ACATATTTGAGAAAC[C/T]GTAAGGTAGAACTAA | 1130 |
rs191140754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848368 | CTATCAAAACCTCTG[C/T]GATGGAGCAAGGGTG | 1130 |
rs191143851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235840918 | GAAGTGAGTGGTAAG[C/G]GAGGGATCAGGACAA | 1130 |
rs191152344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235876310 | AAACACAATCCAATA[C/T]AGTTTTCCCTCCCTC | 1130 |
rs191158341 | snp | A/C | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884323 | GAGACGGGGTTTCAC[A/C]GTTTTAGCCGGGATG | 1130 |
rs191165917 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660606 | CCGGGCGTGGTGGCT[C/T]ACACCTGTAATCCCA | 1130 |
rs191197918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775670 | TTGGTTTAAGGGAAG[C/G]CTACACAGAGAGAAG | 1130 |
rs191203012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775923 | AGGATACTGAACAAG[A/G]TTTATAAGTTTTAGA | 1130 |
rs191232517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235805042 | GAGATAAGGCAACAT[A/G]GAGGCTGGAACTGAA | 1130 |
rs191245072 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235699062 | AGATACAAGGGCAAC[A/T]GTTTTATATCATAGC | 1130 |
rs191254377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665171 | AAGAAGCAATCTATG[G/T]GTACAGTAACAAGGT | 1130 |
rs191280423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736168 | ATCATTTCAGGGACT[A/G]TAAAAGGTGTCACTG | 1130 |
rs191283240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762193 | TGTACAGTATTTGAA[A/G]ATGTTTCAGAGTGAT | 1130 |
rs191292881 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235722332 | ATATGATCCAACATA[A/C]TTTAGCTGCTGTGTT | 1130 |
rs191297367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740458 | GACAACTACTGTCCT[C/G]AATTCTATCGTCATA | 1130 |
rs191314803 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235781374 | TTTAAATAATGGGAG[C/T]TATATCTTGGTAAAC | 1130 |
rs191331402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235671451 | ATTTACTGATTTGTA[C/T]ATGTTGAATCATCTT | 1130 |
rs191355790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235704246 | CTTTACGGTAGAATG[A/G]TTTACATTCTTTTGG | 1130 |
rs191367196 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235689982 | GTTATTTGTTCATCT[C/T]TGTCCTCTCTTCACA | 1130 |
rs191388814 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235858161 | CTACTTTGCAGAAGG[A/C]TAGCATGGTTTAGTA | 1130 |
rs191393854 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884946 | TACAGGAAAACACCA[C/T]CATGCCTAGCTAATT | 1130 |
rs191454196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821249 | TGAAAACAGTCTGGG[C/T]AACACGGTGAAACCC | 1130 |
rs191459412 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822155 | AAAAGGCCTCTGGGC[A/G]CCCACTCTTCAACAG | 1130 |
rs191474959 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235848736 | AAAGATCATTCAAGG[C/T]TACTACGAATACATT | 1130 |
rs191485687 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235706270 | GACTTTTTGGCTTTC[C/T]CCTGAAGCAGATCAT | 1130 |
rs191488271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683191 | CAAAGGCTAATATTA[A/C]TAGACAATTCACTGA | 1130 |
rs191503768 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753954 | GAGACACACGTTTCT[C/T]TCTATTCTATCATAA | 1130 |
rs191510751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714474 | GAGTGAATACAAATT[C/T]ATTCCTCCAATAGGT | 1130 |
rs191518313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785109 | ATTGCTGCAGCCTCC[G/T]GCAGTGATGCCCTGT | 1130 |
rs191525040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743420 | ACATGTCATGATTTA[C/T]GAGTTCTGCTAGAAT | 1130 |
rs191530117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235786295 | ACTCTGACAGATTTG[C/T]AAGTTAAAGTATAGT | 1130 |
rs191537911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767810 | ATGCTATTGAAATCT[G/T]GTAAGTCATTAAGAA | 1130 |
rs191546170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235805301 | CTGAAGTGCCCCACA[A/G]TGATTGTCCCCACTT | 1130 |
rs191546197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738007 | ATACTCTCAAGTATA[C/T]GCTCAAGGATCAGCT | 1130 |
rs191557323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235822385 | GAGATGGCTATGTTC[C/T]TCTCCTGTCCCTCTT | 1130 |
rs191575440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667910 | CTCGTGATCTACCCA[C/T]CTCGGCCTCCCAAAG | 1130 |
rs191599154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700486 | GAAATGCTTTTTATA[C/G]AGCTCTGATTGTTTT | 1130 |
rs191600226 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235716860 | TCTGCATCTTGTAAG[A/T]AGGTAAGTGGTCAAC | 1130 |
rs191615028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235686399 | CAAAACAAAACAAAA[C/T]CCCCCAAAAACAGTA | 1130 |
rs191632788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815403 | AAGGGTAACATTTTA[A/G]ACAGGCTATTTAGGA | 1130 |
rs191637569 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866789 | AGGCCACGCAGAGGG[A/G]CCGGGACCCGGAACC | 1130 |
rs191643398 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235830934 | AATAGCTAAAGTTAC[A/G]CCACTTCACTTCTTA | 1130 |
rs191645024 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235746900 | TCAAGTTTTAATGCA[C/T]ATAATTTTTTAGTAA | 1130 |
rs191648759 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235787586 | AACTAAAATAGATTA[A/G]GCTCATTGGCTGGTA | 1130 |
rs191651320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769576 | TGGAAAATTGTCTAA[C/T]ATACCAACCAAGCAG | 1130 |
rs191665856 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848938 | AGAATTCTACCAGAC[A/G]TTTAAAGAATTGGTA | 1130 |
rs191671702 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867217 | CCGCACCTCCTCCCA[G/T]GGCTCTGCGTAGTGG | 1130 |
rs191678534 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885676 | TATTCTAGTATCTTA[G/T]GTACCATGTAGGTAT | 1130 |
rs191688421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804051 | TGACTGCTATTTTCT[A/G]TGTAGGCACTAGTCA | 1130 |
rs191698663 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235800613 | AATTAAATGCATTTT[A/T]AAAAATATTACCCAG | 1130 |
rs191708376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235727267 | AGCTGGGATTATAGG[C/T]GCCACCACCACAACT | 1130 |
rs191732444 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235708262 | TGGACTTTAAAATTT[C/T]TCCCTGTTGCTAGTC | 1130 |
rs191743606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725156 | AAAGGGGAATAGGCC[A/G]GGTGCGGTGGCTCAT | 1130 |
rs191748012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235721700 | AACATCCTAAACCTG[C/T]AGCCTAAATCTGAAG | 1130 |
rs191757120 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235689438 | TCCTATGTGGAATCT[A/C]AAAAAAGCTGAACTA | 1130 |
rs191763505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235761434 | TCTTCTATAAAGTAG[C/T]GATGAGACTCTGTTA | 1130 |
rs191764297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767149 | TATAAATAAATTGCT[A/T]ATATCCTCCAATTCC | 1130 |
rs191778064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826484 | ATGCAACAACATGGA[C/T]GAATTTCAGAGACAT | 1130 |
rs191815094 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235723961 | CTTCATGTAATCAGT[A/G]TGAGTATAGTTACAG | 1130 |
rs191829381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691388 | ACGAAGCTGGGACAC[C/T]AACAAAGATCACAGG | 1130 |
rs191852371 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235666836 | ATAATTAGATAAGTA[C/T]TAGTAAGGCTAGAAG | 1130 |
rs191932882 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235870575 | AAATTTAATTTGGCT[A/G]AAGTGTTTCTTTTAT | 1130 |
rs191944241 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235845497 | TGCTGGCCAGAACTC[C/T]GGGGAGGGTGCAAAT | 1130 |
rs191946652 | snp | A/C/T | 0.00677135 | 0.0578593 | intron-variant | LYST | GRCh38.p7 | 1:235707495 | AGGTGCGGTGGTGGG[A/C/T]GCCTGTAATCCCAAC | 1130 |
rs191980832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843826 | TTAGAAAGCATACTT[C/T]TTCCTCATCAAACAG | 1130 |
rs191990716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832890 | GGGATTTTGTTTTCC[A/G]TAACATATTCTAGGA | 1130 |
rs191990752 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235877618 | TCCATGTTGGTCAGG[A/C]TGGTCTCGAACTCCC | 1130 |
rs191996235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235810565 | AAGAAGGCTTAGAAT[A/G]CCTCAATATGTTTTA | 1130 |
rs192000372 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235850029 | TAGAAAAAAAAATCT[A/G]AAATTCATATGGAAC | 1130 |
rs192000901 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235818725 | TGGCAGGTGAACTAA[C/T]AGCATTCTAATGGAG | 1130 |
rs192002272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235869193 | GAAAGCTCTACTTGG[C/T]CGGGCGCAGTGGCTC | 1130 |
rs192009075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669523 | CACCTTAGCCTACGA[C/T]TGGTTGCAAAAAGCA | 1130 |
rs192011896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235880194 | TCTCAAACATGTTTC[C/T]TTTTGTATTGACCAC | 1130 |
rs192017654 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | LYST | GRCh38.p7 | 1:235715457 | CTTCTCTACTACCCC[C/G/T]TTGAGGCCATTCTCC | 1130 |
rs192026719 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235693767 | TTATTATAAAAGACA[C/G]TAATAGTGAAGCTTA | 1130 |
rs192033648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677310 | ACATGTTTTCCTATC[C/T]GATTGTATGACTTCA | 1130 |
rs192042307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702448 | TGCTTGAAAAATCCT[A/G]TTATGTCACTGCCCT | 1130 |
rs192056672 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235703296 | ATCCAAAGCAATATA[C/T]AGGAAAAGGCAAAAA | 1130 |
rs192079292 | snp | A/T | 0.131038 | 0.219882 | intron-variant | LYST | GRCh38.p7 | 1:235780420 | TAAAAAAAAAAATAA[A/T]AAATAAAAAAGAGTA | 1130 |
rs192079668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739320 | CACATGCTGCAGTTG[A/G]CCCTTGAGCCAGATG | 1130 |
rs192099362 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235673964 | AGCAGAGACCCAAAT[A/C]GTCCCCTTTCCACTT | 1130 |
rs192131538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705727 | TATAAGAATAACTGA[A/G]AAGATGGTTCAGGAT | 1130 |
rs192140250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST, MIR1537 | GRCh38.p7 | 1:235853047 | AGGACAGAAAACTGA[A/C]TAATTACAGCTGTAC | 1130 |
rs192146411 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235793901 | GCAATGGCATGATCT[C/T]GGCTCACTGCAACCT | 1130 |
rs192183235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712850 | ATAATAAAGAATTAA[A/G]TTTGGACTCTCTTTT | 1130 |
rs192215328 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235819607 | TAGACCACCCAATCA[A/G]GAGAAATCAGCCAAT | 1130 |
rs192218532 | snp | C/T | 0.00160133 | 0.0282507 | intron-variant | LYST | GRCh38.p7 | 1:235792177 | ACGTAATAAAGTACA[C/T]AATAATCTTGAAATT | 1130 |
rs192218843 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235750591 | ATATATGTATGTGTG[C/T]ATATCCTGTGTATGT | 1130 |
rs192219419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750197 | CTACTCAGGACAAAA[A/G]AGATGTACAACTGGG | 1130 |
rs192223990 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854266 | CCTAGTTGACACATA[C/T]TGGAAACTGAAGCAC | 1130 |
rs192230730 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235811017 | AGATGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 1130 |
rs192235815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235873061 | AAGCAGGAGAAAGGA[A/G]GGTGAGAGAAGGTGA | 1130 |
rs192236558 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827096 | AAGCTGGGCGCAGTG[G/T]CTCACACCTGTAATC | 1130 |
rs192245554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827761 | CACCACAGGAAAAAA[A/G]TATTTAACTTATGAC | 1130 |
rs192246232 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235682027 | TCAAAGGGTTATTAC[A/G]AAGATTTAACATGTG | 1130 |
rs192282659 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235733343 | TAAAAAAAACTCATA[C/T]GATTATTCTTTAAGA | 1130 |
rs192294602 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235712386 | TGAGATCATATTACA[G/T]TTTTCATCTGTATTA | 1130 |
rs192338243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235791341 | GGGGCTGGGAAACAA[C/T]AGAAAGAAAGGCAGC | 1130 |
rs192351124 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235688756 | TTGGGAGGCCGAGGC[A/G]GGCGGATCATGAGGT | 1130 |
rs192372802 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235720425 | TGCATACTGTAGAAC[A/C]AAGAAGTGACATAAC | 1130 |
rs192378483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235831757 | TCTCATTCTAAAATA[C/T]GGCAATAACCTCTAT | 1130 |
rs192382117 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868392 | GAAGCCAAACTTAAC[C/T]TGTTTCGTCATTTTA | 1130 |
rs192444218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235872465 | TCGTGGTAATAGACC[A/G]AGGGGGGATCCAGCA | 1130 |
rs192450030 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235797643 | AACTCAAAATGAATT[C/T]AGGATCTAAATGTAA | 1130 |
rs192481945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235692993 | GCTTTTGCACTCCAG[C/T]CTGGGCAACAGAGCG | 1130 |
rs192484303 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235781633 | CTAAGTTAATATGAG[C/T]TTCTCTTTTTTGAGG | 1130 |
rs192493228 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235732316 | TTTCTTTTTCTTTTT[A/C]TTTTTTGACAGGGTC | 1130 |
rs192493676 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819649 | CTTATTTAATACTTT[C/T]ATTTTGTTTTGTTTT | 1130 |
rs192499174 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235802172 | GCACTCTAGCCTGGG[C/T]GACAGAGCAAGACTC | 1130 |
rs192500441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837225 | CCAACACAGGAGACT[A/G]AGAAGGAACAGCAAG | 1130 |
rs192508797 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711175 | TTATACAGCCACAGA[G/T]AGCTAGAACATACAT | 1130 |
rs192517220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853700 | CCTTGAAACCTGGGG[C/T]GCTGACCTAGGGAGG | 1130 |
rs192522246 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235726542 | TATTTGTACACACAT[C/T]TGCACACACAACGCA | 1130 |
rs192522964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835627 | CCAGCACAGTCACAT[A/G]TGTCCTCCTTGAGTC | 1130 |
rs192539305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872110 | TGACCAGCCTGGCCA[A/G]TGTGGCGAAACCCAG | 1130 |
rs192547320 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235762991 | GCATACTTTATATTA[A/C]GGCACACGATATGTG | 1130 |
rs192585883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734214 | CTCTAACTCAAGGTA[C/T]GCTTCAGCTTGCTTG | 1130 |
rs192586640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680966 | ATACATTTATTCATC[C/T]AACAAACATTGTTGA | 1130 |
rs192587760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235696602 | CTCTACTGCACAGCA[C/T]TTTCCCACATGTTGC | 1130 |
rs192602611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235697661 | TGGTAATAGAAATCA[A/G]GACCACATGTAGCAC | 1130 |
rs192603579 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662421 | ACAGAGGCACCTACT[A/G]AATAATTTGCTTCTC | 1130 |
rs192605076 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235801700 | TAGCAAACATAAAAA[A/T]GGAGGAAATCCAAAA | 1130 |
rs192609663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235774363 | AGGGGTGGAGGCAAG[A/G]GTAGAGCAATCGTCT | 1130 |
rs192635240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235878472 | TCAGATACTAGCAAC[C/T]TGAAGTAAAAATAAT | 1130 |
rs192662118 | snp | C/T | 0.00100861 | 0.022434 | intron-variant | LYST | GRCh38.p7 | 1:235663108 | AAATTCCCATTTGTA[C/T]ATTATATTTCTTAAA | 1130 |
rs192697748 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235842045 | GCTATTTCAGATTCA[C/T]CAGCAGGATTCAGCT | 1130 |
rs192718364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700120 | AAATGTAAAACCCAA[A/C]ACCATAAAAACCTTA | 1130 |
rs192729236 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235737712 | AATGACTGCAATAGA[A/C]TAAAACACATAACAT | 1130 |
rs192730393 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235777718 | CTTTGCATTTGCTCA[C/T]TGGCTGACTCTTCAT | 1130 |
rs192741849 | snp | A/C/G | 0.00319074 | 0.0398324 | intron-variant | LYST | GRCh38.p7 | 1:235849402 | ATGACAAACCCACAG[A/C/G]CAACATAATACTGAA | 1130 |
rs192771618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778110 | TTAAATATATATATA[C/T]ATATATATATATTTT | 1130 |
rs192787617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815672 | GCAAACCAAGAACAC[A/C]ATCTCATTCACAACA | 1130 |
rs192793688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707000 | TTATAAACGCTTGTA[A/G]ATTTGCTACAGTCGA | 1130 |
rs192796971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235676357 | TAACATACCAGATCA[A/G]ACAAGAATGGAGTAG | 1130 |
rs192805011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235745847 | ACAAAAATATACAAA[C/T]GGAGGACAGATTAGC | 1130 |
rs192808860 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235823048 | AACTCAACAGAATCA[G/T]GAGCAAAGAAATCAT | 1130 |
rs192814023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858773 | CTCAATCCAGGTTCA[C/G]TCTACTTGTTTTCTG | 1130 |
rs192832341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746260 | TTAAACATCTGAAAA[C/T]CAACCAGTTTCCTCT | 1130 |
rs192853419 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235786815 | CAAAAAACCAAACAC[C/T]GCATGTTCTCACTCA | 1130 |
rs192855066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685074 | CCCCCCAAAATCCCC[A/T]TGCCTTTGATTCCAG | 1130 |
rs192865013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859449 | AAGAATATATTTACT[G/T]AACAAATGAAAATTG | 1130 |
rs192892865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235795809 | GCAACCTAAATCAGT[A/G]AAAATAATATTTAAA | 1130 |
rs192902671 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235823731 | TTTTCATGTGCAATT[C/T]TTCTGGTCTGGTGTT | 1130 |
rs192913849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716003 | TCTGATAACAAAGTC[A/T]GGTATAGTGAATTTT | 1130 |
rs192922169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685794 | GAGATTGCATTGAGC[C/G]AAGATCACACCATTG | 1130 |
rs192927984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863027 | CAAAGTATTAAAAAT[A/G]AGTCATTTCCTTTGT | 1130 |
rs192936306 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235755928 | GACTGGCAGCCTTAG[C/T]TGAGTATAAATAGAA | 1130 |
rs192937964 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235838114 | ATTTGGCAATAGGAG[A/G]ACCAAGAATTTTTTT | 1130 |
rs192971926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764098 | CCTAGTTCCCTGTCA[A/C]GCTGTTTCCTTTACC | 1130 |
rs192972907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235802660 | ACACTAGAATATACA[A/T]GAAATTGGGGACTCT | 1130 |
rs192986205 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662623 | TCATAGAAAAAGGGG[A/T]GACCTTAATATTTTC | 1130 |
rs192998138 | snp | A/G/T | 8.3837e-05 | 0.00647398 | intron-variant | LYST | GRCh38.p7 | 1:235697297 | AGAAAAATAAAAAGT[A/G/T]TGGCTTTTTAAAAGG | 1130 |
rs193022070 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235841679 | ATTGGATCAAGGGTA[G/T]AGGTGAAGAGGTTAG | 1130 |
rs193046342 | snp | C/T | 0.031825 | 0.122064 | intron-variant | LYST | GRCh38.p7 | 1:235726790 | ATAAACCAACATATT[C/T]GACAGATGGACTCAG | 1130 |
rs193054100 | snp | A/G | 8.25048e-05 | 0.00642228 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805887 | TGCTTCCTCGGGAGC[A/G]GCTTCAGTAGCTGAA | 1130 |
rs193056122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235768951 | TTGTGTTTTTGGAAT[C/T]CATTCATTTAACAAA | 1130 |
rs193062638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882807 | GTAAAAACATCCCAC[A/G]TGAGTCCATCTGCAC | 1130 |
rs193068103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666542 | ACTGAATACTTAAAA[A/C]ATGGCTGGAATGGCA | 1130 |
rs193079450 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235699761 | CCTTGACTTTTTAAT[A/G]ATCGCCATTCTGATT | 1130 |
rs193103520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235672749 | ACTAAGTGTTTTCCC[A/G]TTACCCTATTAAGAG | 1130 |
rs193104300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235740820 | TTTTCAGGTAAATAT[A/C]TAAAAATGGAGTAAC | 1130 |
rs193110145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772846 | CCCATATGCTCCTGC[C/T]TGACTGCAGTATTCT | 1130 |
rs193170181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819715 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAAGCTC | 1130 |
rs193171766 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881847 | ACAGAATGGTGGTCG[C/T]CAGAAGCTGGGGGAT | 1130 |
rs193185948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235782395 | AGCCAGGATGGTCTC[C/T]ATCTCCTGACCTCAT | 1130 |
rs193189858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845635 | TGGAAACAGACTCCC[A/G]GCAGTTAGGGGGGAC | 1130 |
rs193194805 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235681385 | GAGGGGTCAGAGCAC[A/G]GGGCCTGGTGTGTGA | 1130 |
rs193255082 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235690609 | GCTATATAACAAATG[A/G]TGGCAATATTTTGGT | 1130 |
rs193255861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749578 | TTAAGATGAGGAAGC[A/T]GGACTGGATGACTTT | 1130 |
rs193263210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235722686 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 1130 |
rs199542846 | snp | A/G | 1.672e-05 | 0.00289132 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766259 | GGGGCATGGGTGTGA[A/G]TTGCCCCTCTTTGTA | 1130 |
rs199552722 | snp | G/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884623 | TTTTTTTTTTTTTTT[G/T]CCGTTCCTTTGTGCT | 1130 |
rs199554293 | snp | C/G/T | 4.95588e-05 | 0.00497768 | synonymous-codon, missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751349 | AACTCTAAGCTGTAG[C/G/T]GCAACAGCCATATCT | 1130 |
rs199576020 | snp | C/G | 8.29236e-05 | 0.00643855 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755637 | GCTCTAGCAAAATAT[C/G]CATCTAATAGCTAAA | 1130 |
rs199582207 | in-del | -/AAT | | | intron-variant | LYST | GRCh38.p7 | 1:235727648 | TATCAGTCTGTCTAG[-/AAT]AATAACAATTATCAT | 1130 |
rs199601043 | in-del | -/AAAG | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235715878 | AGAGATAAAAAAAAA[-/AAAG]AATATGGTGATTTTT | 1130 |
rs199617821 | snp | A/G | 0.000873787 | 0.0208837 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809163 | CACTGATGGGCACAC[A/G]CTGCAATGCAACAGC | 1130 |
rs199631995 | snp | A/G | 0.000612314 | 0.0174866 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753136 | TACCTTAGAACAAGA[A/G]TTTAAAATTTGGAGA | 1130 |
rs199654567 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235816471 | AAATAAAAAAAAAAA[-/A]GCCATACTGCCCAAA | 1130 |
rs199656873 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235666603 | TGCACACACACACAC[-/AT]ACATACACACACACA | 1130 |
rs199663324 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235880192 | GTCTCAAACATGTTT[-/C]CTTTTTGTATTGACC | 1130 |
rs199665324 | snp | A/C | 0.0131955 | 0.0801476 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751353 | CTAAGCTGTAGTGCA[A/C]CAGCCATATCTAAAA | 1130 |
rs199672291 | snp | C/T | 0.000345932 | 0.0131471 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720701 | CAAGTGTCTCACTAA[C/T]GTAGTCAGCAAGTAT | 1130 |
rs199677493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714804 | TCAATAATGTACTTG[C/T]CTTTATAATAAACTG | 1130 |
rs199680727 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | LYST | GRCh38.p7 | 1:235699103 | CATTATTCTCCTTTC[-/T]TTTTTTTTACTTTAG | 1130 |
rs199694469 | snp | G/T | 0.0506409 | 0.150851 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791872 | CCCAGCAACGGCAGG[G/T]GGACTGGGGCTATGT | 1130 |
rs199695792 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235682303 | GTACTCCAGCATGGG[C/G]AAAAGGGCAAGACCC | 1130 |
rs199696176 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764480 | TCATTTACTACATTT[C/T]TTTTTTTTTCTTTTC | 1130 |
rs199703181 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719627 | AACCATGCAGAATGA[A/T]AAAAAAAAAAAAAAG | 1130 |
rs199704748 | snp | C/T | 6.60404e-05 | 0.00574594 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809634 | AGAAGGGCTCTATGA[C/T]GATACTTTGAAAACA | 1130 |
rs199706208 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820517 | TGGGACTACAGGCAC[A/G]TGCCACCACACCTGG | 1130 |
rs199721128 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759401 | AGTGTGTCGGAACTC[C/T]CCAAAGAATTTTGTT | 1130 |
rs199724679 | snp | A/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739620 | AGTGAAAAAAAAAAA[A/T]AGAAAAAAAAAAAAA | 1130 |
rs199727016 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791975 | TTCTCAATAAACCCA[C/T]GGCCTTACTGTTTAA | 1130 |
rs199729572 | snp | A/C/G | 0.000313061 | 0.0125074 | intron-variant | LYST | GRCh38.p7 | 1:235663967 | TTCTGAAGCATAAGA[A/C/G]GGGGAGAAGATCTTA | 1130 |
rs199738377 | snp | A/T | 0.00299557 | 0.0385851 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762650 | ACTTCTAAAATATGT[A/T]CAATTTAATTATCTA | 1130 |
rs199746236 | snp | A/G | 6.59359e-05 | 0.00574139 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806671 | AGGCTGATTATCAGA[A/G]TTTCAAATGCTTTTA | 1130 |
rs199764541 | snp | C/T | 0.001998 | 0.0315438 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702907 | GTCTGCCCGTAGGTT[C/T]TTATCATGGTTTCTA | 1130 |
rs199768620 | snp | C/T | 9.90802e-05 | 0.00703778 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792038 | TGCTTAAATTTGGAG[C/T]GTGCAGTAAAGGGAA | 1130 |
rs199776717 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | LYST | GRCh38.p7 | 1:235733817 | CATGCCTTTGGAACA[C/T]ATAAAATCTTACCTT | 1130 |
rs199814905 | snp | A/C/T | 0.000230742 | 0.0107389 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787366 | CATCATTTGAATCCA[A/C/T]GCACACACTACAGAA | 1130 |
rs199844506 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235681828 | TCCCTTCTTTCCTCA[-/T]TTTTTTTCTTTATCT | 1130 |
rs199855658 | snp | C/T | 0.000369468 | 0.0135867 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800912 | TTTCTTTCTGCCTAA[C/T]AATTTTCAAAAAACT | 1130 |
rs199857997 | snp | A/G | 0.00046641 | 0.0152639 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759562 | ACGCAGCATATGGGC[A/G]GCCATCTGTTGTGGA | 1130 |
rs199865845 | in-del | -/TATA | 0.030665 | 0.119967 | intron-variant | LYST | GRCh38.p7 | 1:235817373 | AATCCCATTATTGGG[-/TATA]TATATACCCAAAGGA | 1130 |
rs199889667 | snp | A/C/G | 0.0040146 | 0.0446238 | intron-variant | LYST | GRCh38.p7 | 1:235664658 | GCGGGTTACCAGAAT[A/C/G]TGGCTGTCTCAGAGC | 1130 |
rs199898370 | snp | C/G | 0.000198226 | 0.00995357 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801071 | TTGATGCACTGAAAC[C/G]TTCTGTTTCAGACTT | 1130 |
rs199914893 | in-del | -/TA | 0.0948562 | 0.196037 | intron-variant | LYST | GRCh38.p7 | 1:235730564 | ATATATATACATATT[-/TA]TATGTGTGTGTGTGT | 1130 |
rs199926046 | snp | C/T | 5.00663e-05 | 0.00500307 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734658 | ACTAACTTGGCTCCA[C/T]GCTTTAAAAAAAGTA | 1130 |
rs199934421 | snp | C/T | 3.30295e-05 | 0.0040637 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805774 | AATTCCATCTTCTGT[C/T]GACTAGTTCTGGCAC | 1130 |
rs199934732 | snp | C/T | 0.00199806 | 0.0315443 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809581 | TTTGAAGACAACAGA[C/T]CAGAATCTGAAGAAC | 1130 |
rs199944067 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235749780 | AAAATGACTCAAACT[-/A]AAAAAAAAATAATAA | 1130 |
rs199949103 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235744903 | ATCTCAAAAAAAAAA[A/G]GAAAAAAAAAAAGAG | 1130 |
rs199961783 | snp | A/C | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661198 | AAATAATCCCCCCAA[A/C]TTAATTTTTATTTTT | 1130 |
rs200002092 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827944 | AATAAATAACCTGAC[C/T]TTAAAAATGGTACAA | 1130 |
rs200028327 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235695626 | AAACTTTACAGTACT[C/T]TAATTTTTTTTTTTT | 1130 |
rs200036320 | in-del | -/TG | 0.0174175 | 0.0916809 | intron-variant | LYST | GRCh38.p7 | 1:235807345 | AAAGTTTTTCAGCTC[-/TG]TCTCAGGTGAGACTT | 1130 |
rs200038014 | snp | G/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731116 | TCCTCTCTCGATTTG[G/T]CCCTTCTGTTGGATC | 1130 |
rs200041286 | snp | A/C | 0.000858133 | 0.0206961 | intron-variant | LYST | GRCh38.p7 | 1:235782098 | GCTTCCTACATTAAA[A/C]ACAAAACAAAGTTAA | 1130 |
rs200044710 | snp | C/T | 4.98998e-05 | 0.00499474 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808915 | AAATATTACAAGCTG[C/T]TTTTTTAATTTTTGG | 1130 |
rs200051317 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882153 | TGGAGGAAGGAGGAT[C/T]GGGAAGGCTTCACAA | 1130 |
rs200080851 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673220 | TAATCAGTCTGTCTC[-/T]TTTTTTTTTCTCTTC | 1130 |
rs200095105 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830089 | TATAAATAGGTCCAC[-/T]TTTTTTTTTAGTGGA | 1130 |
rs200108337 | snp | C/T | 0.000617212 | 0.0175563 | intron-variant | LYST | GRCh38.p7 | 1:235716824 | ATATTTTGATACTGT[C/T]AAGATTAAGCTCCCT | 1130 |
rs200125599 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718376 | ACTTTTTTTTTTTTT[-/C]CAGACAGTTTCACTC | 1130 |
rs200129772 | snp | C/T | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773852 | CATGCCTCTGCTTTA[C/T]TCCATATCTTCCAGT | 1130 |
rs200132460 | snp | C/T | 0.000609721 | 0.0174496 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830275 | AGAAATCCTCGACCA[C/T]GGACAAGGTACTGTC | 1130 |
rs200143565 | snp | C/T | 0.000494641 | 0.0157187 | intron-variant | LYST | GRCh38.p7 | 1:235677460 | AATGCTATGTTTGAT[C/T]TGGAGACCTTCTTCT | 1130 |
rs200155335 | snp | A/C | 0.00199805 | 0.0315441 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744155 | TAATGTCTGAATTAA[A/C]TTCTTTGAATTGAAA | 1130 |
rs200175567 | snp | C/T | 3.31587e-05 | 0.00407164 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762803 | CCTCCACTGCTGGAA[C/T]GCCTCAGGTACATGA | 1130 |
rs200179826 | snp | A/C | 4.95176e-05 | 0.00497558 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806391 | GGCCGACTCCCTGTC[A/C]GACTCTGCTTCTTTA | 1130 |
rs200189506 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235791291 | GTCTCAAAAAAAAAG[C/T]GAGAGAAAGAAAAGG | 1130 |
rs200218973 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235798577 | GGGCAAAACCCTGTC[-/A]TAAAAAAAAAAAAAA | 1130 |
rs200221983 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705383 | TCAGTCTTCAGATAC[-/T]TTTTTTTTAAAAAAA | 1130 |
rs200223849 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235748358 | TTAAAAGTATATATT[-/G]CTACCTTATTTATAA | 1130 |
rs200231136 | snp | A/C | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759116 | GGAAAAGCTAGCCCA[A/C]GGCTTGCAATAGTGC | 1130 |
rs200246834 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235737043 | CTATAAAACAAACTG[A/G]AAAAAAAAGCCTACC | 1130 |
rs200254069 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752228 | AAAAAGAACAAATAA[G/T]TTAAGACACAGCTAA | 1130 |
rs200276917 | snp | A/G | 0.000148298 | 0.00860971 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791906 | AAGATGAAAGCAGCC[A/G]ATGGGGAAAACTCTC | 1130 |
rs200285655 | snp | C/T | 0.00258472 | 0.0358564 | intron-variant | LYST | GRCh38.p7 | 1:235702727 | TTTTGCTGCACTCGA[C/T]TGAAATCCAAATGAC | 1130 |
rs200294024 | snp | A/G | 1.65789e-05 | 0.0028791 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766185 | TGTCAATAATTCCAA[A/G]TCTGGAGGAGATCCA | 1130 |
rs200306901 | snp | A/C | 3.2993e-05 | 0.00406145 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792029 | AAACACCGTTGCTTA[A/C]ATTTGGAGCGTGCAG | 1130 |
rs200307830 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235801397 | TTTAAAAAAAAAAAA[-/A]CCTATTCAAACTTTC | 1130 |
rs200310900 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235715869 | GCAGTTATCAGAGAT[-/A]AAAAAAAAAAAGAAT | 1130 |
rs200312061 | snp | A/C | 0.00199792 | 0.0315431 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808899 | TCAGAGTCAACAGTA[A/C]AAATATTACAAGCTG | 1130 |
rs200324240 | snp | C/T | 6.6048e-05 | 0.00574627 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806479 | TGGTTAACAGTCTTC[C/T]GTCTCTTTGGATAAG | 1130 |
rs200349572 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854900 | TAAAAATGTTACTCA[C/T]ATCCCTTGGAATGAC | 1130 |
rs200353560 | snp | C/T | 0.000445739 | 0.0149222 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733680 | GATTTTGAATCCAGA[C/T]GCTGAAAGAGACTAA | 1130 |
rs200372187 | in-del | -/TTTC | | | intron-variant | LYST | GRCh38.p7 | 1:235754226 | CTTTTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTT | 1130 |
rs200381196 | snp | A/G | 8.27246e-05 | 0.00643082 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741522 | GCAGCGTGGGCTGGC[A/G]ACAAAATATGCACTA | 1130 |
rs200381916 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759374 | ATGAATGCGTCCTCT[C/T]TGCCTTTTTTCAGTG | 1130 |
rs200403557 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759367 | GCTACTGATGAATGC[A/G]TCCTCTTTGCCTTTT | 1130 |
rs200410409 | in-del | -/AG | | | intron-variant | LYST | GRCh38.p7 | 1:235744903 | ATCTCAAAAAAAAAA[-/AG]AAAAAAAAAAAGAGA | 1130 |
rs200418466 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235685869 | ACAAAAAAAAAAAAA[-/C]AAACAAAAAAAGAAA | 1130 |
rs200437063 | snp | C/T | 1.6696e-05 | 0.00288924 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752079 | ATAACCCTAAAATAT[C/T]GTGAGCCTGAGGAAC | 1130 |
rs200456494 | snp | A/G | 3.30164e-05 | 0.00406289 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805812 | ACAAATGGCCAGAAG[A/G]GCTTCCAAAAGTCGT | 1130 |
rs200468979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732774 | GTGTTCATGCCTTTT[G/T]CTCATTCAAACTTCT | 1130 |
rs200504372 | in-del | -/AAT | | | intron-variant | LYST | GRCh38.p7 | 1:235678128 | GACCTTTGGGAAATA[-/AAT]AATTAAAGTTTTTTA | 1130 |
rs200511787 | snp | A/G | 0.000296589 | 0.012174 | missense | LYST | GRCh38.p7 | 1:235697170 | CCTGGAGAGAGCCAA[A/G]TCTTTCTCCGTGGGG | 1130 |
rs200512692 | snp | C/T | 0.000363498 | 0.0134765 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773952 | CTCCATTCTCATTCA[C/T]ATAAATAATATCTTC | 1130 |
rs200512912 | snp | A/T | 1.70258e-05 | 0.00291764 | intron-variant | LYST | GRCh38.p7 | 1:235663103 | AAAAAAAATTCCCAT[A/T]TGTACATTATATTTC | 1130 |
rs200557017 | snp | A/G | 8.25798e-05 | 0.00642519 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809578 | CACTTTGAAGACAAC[A/G]GATCAGAATCTGAAG | 1130 |
rs200558668 | in-del | -/TATAT | 0.0894459 | 0.191631 | intron-variant | LYST | GRCh38.p7 | 1:235805601 | CATATATAAAAGTAA[-/TATAT]TATATGTTATATATA | 1130 |
rs200565349 | in-del | -/TTC | | | intron-variant | LYST | GRCh38.p7 | 1:235783886 | AAATTCTTTTTTTTT[-/TTC]TTTTAAATTGAGACA | 1130 |
rs200569079 | snp | A/G | 3.31022e-05 | 0.00406817 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773877 | TCCAGTCAAGCAATA[A/G]TTCCTCTAACAGCTT | 1130 |
rs200583452 | snp | C/T | 0.000164172 | 0.00905865 | intron-variant | LYST | GRCh38.p7 | 1:235712220 | AAAATACAAATAATA[C/T]GATTAAGACACAAAG | 1130 |
rs200610828 | snp | A/G | 0.000185424 | 0.00962692 | synonymous-codon | LYST | GRCh38.p7 | 1:235709265 | AGGGGGAAGGTTGAC[A/G]TGATTAACCCGTTCA | 1130 |
rs200639314 | snp | C/G | 0.00199792 | 0.0315431 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702795 | CTCCCTGAAAGCAAA[C/G]TGCACTAGCAACCCC | 1130 |
rs200653684 | in-del | -/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868909 | CATGTTGGTCAGGCT[-/G]GTCTCGAACTCCTGA | 1130 |
rs200659952 | snp | G/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739622 | TGAAAAAAAAAAATA[G/T]AAAAAAAAAAAAACG | 1130 |
rs200691096 | snp | A/G | 0.000164745 | 0.00907442 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791977 | CTCAATAAACCCATG[A/G]CCTTACTGTTTAAAA | 1130 |
rs200703844 | in-del | -/AAG | 0.0543475 | 0.155628 | intron-variant | LYST | GRCh38.p7 | 1:235715879 | GAGATAAAAAAAAAA[-/AAG]AATATGGTGATTTTT | 1130 |
rs200714576 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841315 | GCATAGGTTAAGGAA[-/T]TTTTTTTTTTCAAGT | 1130 |
rs200717661 | snp | A/G | 0.000255988 | 0.0113105 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808425 | TGCTCAACAACCCCC[A/G]CCCCCGCCGCCACCC | 1130 |
rs200728671 | snp | G/T | 0.00199794 | 0.0315433 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800341 | AATCAGAATCATCCT[G/T]TGTTAAAATACTCAA | 1130 |
rs200741121 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235840102 | GCCAGCTATCATTTA[A/C]AAAACAACCACTTTG | 1130 |
rs200753782 | snp | A/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753239 | ACAGACCACTTCTGA[A/G]ACAATCCCATGTTTC | 1130 |
rs200787319 | in-del | -/AA | 0.0850919 | 0.187897 | intron-variant | LYST | GRCh38.p7 | 1:235791280 | GAGTGAAACTGTCTC[-/AA]AAAAAAAAAGAGAGA | 1130 |
rs200787730 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810369 | ACAGAATAGCGATGG[A/G]TAATTTTACGCTGTC | 1130 |
rs200793880 | snp | G/T | 1.64961e-05 | 0.00287189 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809374 | TCACTTTTTTGACAG[G/T]GCTCATTATTTTCAT | 1130 |
rs200797071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823711 | TTTTCTCTAGCCCCC[A/G]TGTTTTTTCATGTGC | 1130 |
rs200807258 | in-del | -/C | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235685059 | GGAAAGTATTTGCCA[-/C]CCCCCAAAATCCCCA | 1130 |
rs200811386 | snp | A/G | 0.000215873 | 0.010387 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810002 | ATGATTCAAGGTAAC[A/G]TCAAACTTACAAACT | 1130 |
rs200812713 | snp | C/T | 6.59739e-05 | 0.00574305 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809052 | GGAATGATTACAGAT[C/T]TGGGATCCATACAAC | 1130 |
rs200813210 | snp | C/T | 0.00218896 | 0.0330104 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734521 | CTGCTTTTGTTGATG[C/T]ACTGGGAGGGATGCA | 1130 |
rs200838035 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | LYST | GRCh38.p7 | 1:235813669 | AAAATACATACACAT[-/A]AAACAGTTAAAGAAC | 1130 |
rs200838063 | in-del | -/CA | | | intron-variant | LYST | GRCh38.p7 | 1:235680019 | ACACACACACACACA[-/CA]ACTAAGACTGAATAA | 1130 |
rs200848640 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235876362 | ATTGTTATTTTCTTT[-/A]AAAAAAAATGGTTTG | 1130 |
rs200848982 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235805637 | ACAATAATATATATA[-/T]TTACATATATTATGT | 1130 |
rs200850318 | in-del | -/T | 0.0236746 | 0.106192 | intron-variant | LYST | GRCh38.p7 | 1:235754718 | ATTACTTTTAGCAGA[-/T]TTTTTTCTAAAGGTG | 1130 |
rs200876896 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759334 | TTCCATTTCACAAAC[A/G]GTTTTTGCAGACTCA | 1130 |
rs200877751 | snp | C/T | 0.00021464 | 0.0103573 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770293 | AAAGTTTCCCAAACA[C/T]CTTGCTGAAGAGATA | 1130 |
rs200884014 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235836241 | ATTCAACAAATGTTA[C/T]TGAACATTTACTGTA | 1130 |
rs200884373 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810257 | TAAAAAATGATGCAG[C/T]AGATGGGGCCTTCTA | 1130 |
rs200888557 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235733949 | TATAAAATTTATTAT[G/T]TCTCACCTAACATTG | 1130 |
rs200904504 | in-del | -/AT | 0.0162398 | 0.0886349 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884768 | TAGAAACTTTTGTAC[-/AT]ATATATATATAAACA | 1130 |
rs200911918 | in-del | -/ATCTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235755999 | ATGCTCTCTCTGCAA[-/ATCTAT]ATCTATATCTATATC | 1130 |
rs200927646 | snp | C/T | 0.000130195 | 0.00806725 | intron-variant | LYST | GRCh38.p7 | 1:235805701 | GTGTGTATATATATG[C/T]ATATATATTACATAA | 1130 |
rs200935378 | snp | A/G | 0.000148335 | 0.00861078 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830306 | CAAGGGTTGCCATGT[A/G]CGTCTCCTCCTCTTC | 1130 |
rs200941072 | snp | C/T | 0.000659022 | 0.0181405 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662935 | AACGTGAAGTTCATT[C/T]GCATTCACCCGGCTG | 1130 |
rs200950899 | in-del | -/AT | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235818021 | GAGATTTATACACAC[-/AT]GTCAATTTTGCAATG | 1130 |
rs200965362 | snp | A/C/T | 0.00130958 | 0.025556 | intron-variant | LYST | GRCh38.p7 | 1:235810557 | AATGAAAAAAGAAGG[A/C/T]TTAGAATACCTCAAT | 1130 |
rs200967528 | snp | A/G | 4.55976e-05 | 0.00477459 | intron-variant | LYST | GRCh38.p7 | 1:235746533 | TTTCGAGGACCTTTA[A/G]AAGTATATAAATTAA | 1130 |
rs200984503 | snp | G/T | 0.000131996 | 0.00812284 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801053 | GTAAGTCATTTGGAC[G/T]GCTTGATGCACTGAA | 1130 |
rs201016953 | in-del | -/A | 0.0221141 | 0.102801 | intron-variant | LYST | GRCh38.p7 | 1:235850017 | TCTTCACAGAATTAG[-/A]AAAAAAAATCTAAAA | 1130 |
rs201023832 | snp | A/C/T | 8.25572e-05 | 0.00642437 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830348 | CCTCCACCCTCTGGA[A/C/T]CACTGCATTGCAAAG | 1130 |
rs201025005 | snp | A/T | 1.65754e-05 | 0.00287879 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766175 | TGAAGATAATTGTCA[A/T]TAATTCCAAATCTGG | 1130 |
rs201026377 | snp | G/T | 6.59402e-05 | 0.00574158 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810133 | TTGACCCCTGTCTTG[G/T]AATAATCTCTCTGGA | 1130 |
rs201030859 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235730612 | GTGTGTGTGTGTGTG[C/T]GTATATGTAAACTAA | 1130 |
rs201035814 | snp | A/C | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787259 | TTTCCCTTGGGGCTG[A/C]TGTAAGTAGGTGAGT | 1130 |
rs201037421 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235874238 | CACAGAATCCACTAC[A/G]GTAGTAAGATTGCAG | 1130 |
rs201038850 | snp | A/G | 9.89299e-05 | 0.00703244 | intron-variant | LYST | GRCh38.p7 | 1:235677074 | CAGCCCTGTGCTTTG[A/G]GTTGGAGCAAGCTCA | 1130 |
rs201043240 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752869 | AATACAATTTCTTGC[-/T]TTTTTTTTTCTTTCT | 1130 |
rs201045270 | snp | A/G | 0.00025168 | 0.011215 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235743979 | AATTAATTTACTTAC[A/G]ATAGATACTTTGAAT | 1130 |
rs201065186 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235726666 | ATTTGAAAAAAAAAT[G/T]TTCCTCTTTATTTAA | 1130 |
rs201085929 | snp | C/T | 0.000148325 | 0.00861049 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804523 | TCAGTCATAGCATCA[C/T]TATGTTCAAAATCTG | 1130 |
rs201093045 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822017 | ATAGATGTGGCTTTT[G/T]AGGCATAGAGTGAAC | 1130 |
rs201095810 | snp | A/C/T | 1.66004e-05 | 0.00288096 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759548 | GGTAGGCTTCTAGAA[A/C/T]GCAGCATATGGGCGG | 1130 |
rs201106245 | snp | G/T | 0.000395804 | 0.0140622 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809154 | AAGCGCAAGCACTGA[G/T]GGGCACACACTGCAA | 1130 |
rs201106263 | snp | A/G | 0.206336 | 0.246157 | intron-variant | LYST | GRCh38.p7 | 1:235851188 | TATGTATATGTGTGT[A/G]TATATATATATATAT | 1130 |
rs201108676 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235763417 | TTGACCACTACCTTT[-/C]CTTTATCCATGGCAA | 1130 |
rs201111880 | in-del | -/AAAC | | | intron-variant | LYST | GRCh38.p7 | 1:235862797 | CAAGTCTCCATCTCA[-/AAAC]AAACAAACACACACA | 1130 |
rs201117816 | snp | A/G | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777164 | TCTTTAGATGATGAG[A/G]TTCTAATAAGATGCT | 1130 |
rs201134063 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235756195 | AATTAATCCTTCCAC[-/CT]CTTTCTCCCCTTCAA | 1130 |
rs201154390 | snp | A/G | 4.9611e-05 | 0.00498026 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757323 | TGATGGGTGGTTAAC[A/G]AGGACCAAAAGTGTA | 1130 |
rs201238085 | in-del | -/TGTGTGTGTGTGTGTA | | | intron-variant | LYST | GRCh38.p7 | 1:235730600 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTA]TATGTAAACTAACAA | 1130 |
rs201238774 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235694011 | TCTTCTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 1130 |
rs201246652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807749 | AGTCTGGAAAACTCA[C/T]TGATAGGATTAAAAG | 1130 |
rs201255245 | snp | C/T | 0.00086383 | 0.0207646 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808668 | CCTTTCTGGATTAAA[C/T]TGCAAATGTGATTTG | 1130 |
rs201266921 | snp | A/C | 0.00169881 | 0.029095 | intron-variant | LYST | GRCh38.p7 | 1:235728164 | ATATAAGGGTTTTAA[A/C]ATGTATGTGCACACT | 1130 |
rs201295320 | snp | A/G | 1.65021e-05 | 0.00287241 | missense | LYST | GRCh38.p7 | 1:235697214 | ACCACAGGTACTGGA[A/G]CACTGGGGGAACCCA | 1130 |
rs201301303 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753232 | AGGAATGACAGACCA[A/C]TTCTGAAACAATCCC | 1130 |
rs201317160 | snp | G/T | 6.5925e-05 | 0.00574092 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759399 | TCAGTGTGTCGGAAC[G/T]CCCCAAAGAATTTTG | 1130 |
rs201320321 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746396 | GTCTCTGCGCAAGTT[C/T]CGTTTCAGTTGCTTG | 1130 |
rs201321308 | snp | C/T | 4.94271e-05 | 0.00497102 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734560 | CACATAACTTCAAAG[C/T]ATTCATAAGCAGTTC | 1130 |
rs201331643 | snp | C/G/T | 3.30656e-05 | 0.00406595 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802989 | CTAAAAGTTTAAAAC[C/G/T]ACAACACTGAGAATC | 1130 |
rs201337542 | snp | C/T | 0.000149357 | 0.00864037 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809869 | AAGCCACCGGTTCTT[C/T]GGTCCAACCTGCAGA | 1130 |
rs201344329 | snp | A/C | 0.000369171 | 0.0135812 | intron-variant | LYST | GRCh38.p7 | 1:235793650 | AAATTAAAGCTAGTA[A/C]ACAATTAGAGGAATA | 1130 |
rs201369759 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235779893 | GAAAGAGGAACCCAG[C/T]TTCATGGCCAGATCT | 1130 |
rs201382097 | snp | C/T | 0.00192684 | 0.0309792 | intron-variant | LYST | GRCh38.p7 | 1:235782091 | ACATCAGGCTTCCTA[C/T]ATTAAAAACAAAACA | 1130 |
rs201398337 | snp | A/G/T | 0.00305926 | 0.0389911 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808451 | CACCCACACACATAC[A/G/T]AACCTGGATTTAAGC | 1130 |
rs201399414 | in-del | -/C/G | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235801423 | TTTCTGACCCCCCCC[-/C/G]TCAAATACCTAAATC | 1130 |
rs201404906 | in-del | -/T | 0.0156448 | 0.0870496 | intron-variant | LYST | GRCh38.p7 | 1:235762864 | CATCTAGAATCCAAA[-/T]TTTTTTTGAAACAGC | 1130 |
rs201412615 | snp | C/T | 0.00054394 | 0.0164825 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809324 | TCGTCTGTGCCTTTT[C/T]CTTGTACACATCGAA | 1130 |
rs201424017 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715626 | AAAACCTACCTAACT[G/T]TGAGCACTCCACCTC | 1130 |
rs201428941 | snp | A/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739624 | AAAAAAAAAAATAGA[A/G]AAAAAAAAAAACGTA | 1130 |
rs201432504 | in-del | -/TGTGTG | | | intron-variant | LYST | GRCh38.p7 | 1:235730568 | ATATACATATTTATA[-/TGTGTG]TGTGTGTGTGTGTGT | 1130 |
rs201436355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845211 | TCTCCTGAACACACA[A/C]CCCCACTGGAGAAGC | 1130 |
rs201440611 | snp | A/G | 3.30213e-05 | 0.00406319 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806412 | TGCTTCTTTACTTAC[A/G]CATAAAAAAGCCACA | 1130 |
rs201461433 | snp | A/G | 0.00199792 | 0.0315431 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808911 | GTACAAATATTACAA[A/G]CTGCTTTTTTAATTT | 1130 |
rs201464237 | snp | A/C/T | 0.000494037 | 0.0157093 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808424 | ATGCTCAACAACCCC[A/C/T]GCCCCCGCCGCCACC | 1130 |
rs201502579 | snp | C/T | 4.94254e-05 | 0.00497094 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791971 | GCTCTTCTCAATAAA[C/T]CCATGGCCTTACTGT | 1130 |
rs201502944 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235761775 | GATTAAAAAAAAAAC[-/A]AAAAAAAAACCAGAA | 1130 |
rs201503994 | snp | C/T | 0.000271993 | 0.0116586 | intron-variant | LYST | GRCh38.p7 | 1:235773830 | AATGGAAAAAAAGTA[C/T]ATATTACATGCCTCT | 1130 |
rs201504222 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235697409 | TAATTATTTTACGCA[-/T]TTTTTTTTTACTTCC | 1130 |
rs201512744 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235760188 | TGATAGTGAAGTGGT[C/G]CAAGGTAAATCACTT | 1130 |
rs201513511 | snp | C/T | 0.000922433 | 0.0214561 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759366 | AGCTACTGATGAATG[C/T]GTCCTCTTTGCCTTT | 1130 |
rs201523144 | in-del | -/CTTATTTCCTAG | 0.0279526 | 0.114869 | intron-variant | LYST | GRCh38.p7 | 1:235737391 | CTTTCTAAAAAAATA[-/CTTATTTCCTAG]CTTTGTCCACTAAAA | 1130 |
rs201554916 | snp | A/G | 8.24097e-05 | 0.00641857 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806266 | TCTGCTGCTTGGTGC[A/G]TATGTTCAGGAGAAG | 1130 |
rs201566191 | snp | C/T | 1.658e-05 | 0.00287919 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757305 | ACCTTGTTGTATAGC[C/T]GGTGATGGGTGGTTA | 1130 |
rs201576299 | snp | A/T | 1.64787e-05 | 0.00287038 | missense | LYST | GRCh38.p7 | 1:235697169 | GCCTGGAGAGAGCCA[A/T]ATCTTTCTCCGTGGG | 1130 |
rs201630951 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235874837 | ATATGGTTGTTATTT[A/C]TATGGGCGTGTGTGT | 1130 |
rs201657364 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731164 | GATAGTAGATGGGGT[C/T]ATACCATACTGCTCT | 1130 |
rs201664687 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235834553 | CAGGAGTGATCTTTA[A/C]TTACTTCAAAATGCT | 1130 |
rs201677077 | snp | A/G/T | 0.00020104 | 0.0100241 | intron-variant | LYST | GRCh38.p7 | 1:235788886 | TCAGTAAAATGGTTC[A/G/T]TAACAACTGAGTAGA | 1130 |
rs201682120 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731165 | ATAGTAGATGGGGTC[A/G]TACCATACTGCTCTG | 1130 |
rs201685064 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235816470 | AATAAAAAATAAAAA[A/T]AAAAAAAAAAAGCCA | 1130 |
rs201693038 | snp | A/G | 0.00896934 | 0.0663643 | intron-variant | LYST | GRCh38.p7 | 1:235724218 | AATATTTGTTTTACC[A/G]GAAATATAAATAATT | 1130 |
rs201694319 | snp | A/G | 0.000114168 | 0.00755454 | stop-gained | LYST | GRCh38.p7 | 1:235712144 | CAAAAGATGAGAGTC[A/G]CCAAGTTGTATTTGT | 1130 |
rs201703229 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791923 | TGGGGAAAACTCTCT[C/T]TATCAGCCTCTTTCT | 1130 |
rs201774077 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235685858 | TTAAAACAAAACAAA[-/C]AAAAAAAAAACAAAC | 1130 |
rs201782716 | in-del | -/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867533 | CAGTGCAGTGGTGTA[-/T]TTTCCAACCGACTCC | 1130 |
rs201788404 | snp | C/G | 0.000399281 | 0.0141238 | missense | LYST | GRCh38.p7 | 1:235687004 | CCGCATTTGCTTCCA[C/G]TAAACAGCTGGCAAC | 1130 |
rs201810135 | in-del | -/A | 0.130694 | 0.219696 | intron-variant | LYST | GRCh38.p7 | 1:235880413 | TATTCTAAGTCAAGG[-/A]ATCCTGTGTTGATTT | 1130 |
rs201820026 | snp | C/G/T | 0.000395855 | 0.014064 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809038 | AAGCATGGAGCAAAG[C/G/T]AATGATTACAGATTT | 1130 |
rs201821563 | snp | G/T | 0.00114323 | 0.0238811 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753119 | TCCAGCAACATATCT[G/T]CTACCTTAGAACAAG | 1130 |
rs201842746 | snp | C/G | 8.4163e-05 | 0.00648648 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759587 | TGTGGAATAATATTA[C/G]AGGAATTCTCTCCTG | 1130 |
rs201847422 | snp | A/G | 3.29973e-05 | 0.00406172 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810397 | GTCGTCTGCTTTTTC[A/G]AAAAACATTTACTTT | 1130 |
rs201852938 | snp | C/T | 0.000148646 | 0.0086198 | intron-variant | LYST | GRCh38.p7 | 1:235677041 | ACCACTGGCCGAATG[C/T]GCTGTTAGAGCACCA | 1130 |
rs201879626 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235874274 | ATCTGTTATTTCAGA[A/C]CTTCATTCAGTTATT | 1130 |
rs201902209 | snp | C/T | 0.00199795 | 0.0315433 | intron-variant | LYST | GRCh38.p7 | 1:235758953 | AAGGTGGGAGGAGTG[C/T]ACAAAAACACATAAG | 1130 |
rs201940074 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235780417 | TCTTAAAAAAAAAAA[-/T]AAAAAATAAAAAAGA | 1130 |
rs201950277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774877 | ATGAGTATCACTGCA[G/T]ATGAAACTATAAGAA | 1130 |
rs201984316 | snp | C/T | 1.66015e-05 | 0.00288105 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773850 | TACATGCCTCTGCTT[C/T]ACTCCATATCTTCCA | 1130 |
rs202010795 | snp | C/T | 0.000468087 | 0.0152913 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235743987 | TACTTACAATAGATA[C/T]TTTGAATCCTTCTAC | 1130 |
rs202023487 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | LYST | GRCh38.p7 | 1:235820381 | TTTTCTTTCTTTTTT[-/A]TTTTTTGAGACAGGG | 1130 |
rs202027621 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235732008 | AGAAATAAATAAGAG[-/A]AAAAAATACCCTTAT | 1130 |
rs202029268 | in-del | -/AA | 0.495291 | 0.0482933 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739623 | GAAAAAAAAAAATAG[-/AA]AAAAAAAAAAACGTA | 1130 |
rs202030647 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235869483 | TCTCAAAAAAAAAAA[-/T]AATAATTAAAAAAGC | 1130 |
rs202037607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813106 | TTCTAAGGCGATAAG[A/C]CACATCAGTTCCTAA | 1130 |
rs202052841 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235724946 | TCTGTTGTATGTGTC[C/T]GCATATGCATGCATG | 1130 |
rs202083549 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235728338 | CTTAATTTCTTTATT[-/A]AAAAAAAAGGTTGCA | 1130 |
rs202107079 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235795354 | TGTAACTGTACAGTC[-/T]GCAGACTGAACAAAC | 1130 |
rs202126320 | in-del | -/GT | 0.0146672 | 0.084371 | intron-variant | LYST | GRCh38.p7 | 1:235700461 | AATATTTAAAGAGGA[-/GT]GCTTTATTGAAATGC | 1130 |
rs202130370 | in-del | -/TTCCCTGCCCTCCCTC | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865304 | GCAAACCTCTCCCGG[-/TTCCCTGCCCTCCCTC]TTCCCTGCCCTCCCT | 1130 |
rs202138033 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809314 | AATATTCACATCGTC[G/T]GTGCCTTTTTCTTGT | 1130 |
rs202146845 | snp | A/T | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741509 | CTTTCTCTCTTGTGC[A/T]GCGTGGGCTGGCGAC | 1130 |
rs202148554 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235850681 | TCAAACAAATCAGTA[A/G]GAAAAAAACAATCCC | 1130 |
rs202185548 | snp | C/T | 0.00199801 | 0.0315438 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744058 | GAAGACTGTTCATGA[C/T]GAATATTTTCCTCAG | 1130 |
rs202198898 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872296 | GTGACATTCTGTCTC[A/G]AAAAAAAAAAAAAAA | 1130 |
rs202201080 | snp | C/T | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766111 | TAGAAGTTCGTGGGA[C/T]TGTGACAAACGTAAG | 1130 |
rs202211458 | snp | G/T | 0.00199802 | 0.0315439 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787296 | TGTTGCCATTTGCTT[G/T]GGAGGAAAATATTCT | 1130 |
rs202217190 | in-del | -/TTTTC | | | intron-variant | LYST | GRCh38.p7 | 1:235754215 | ACATGAGCTATCTTT[-/TTTTC]TTTTCTTTTCTTTTT | 1130 |
rs202226437 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759118 | AAAAGCTAGCCCAAG[C/G]CTTGCAATAGTGCTG | 1130 |
rs202230209 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715881 | GATAAAAAAAAAAAA[C/T]AATATGGTGATTTTT | 1130 |
rs202235200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794272 | TCTTATCTTGAAAAT[A/G]TTTAAATTATATCTA | 1130 |
rs207461245 | snp | C/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712756 | CTGAGCTAAAGAATT[C/G]AGTAAAATTTCCTGT | 1130 |
rs267598424 | snp | A/G | | | missense | LYST | GRCh38.p7 | 1:235663993 | TCTTACCTGATGATG[A/G]GCTTATTTGATTTGG | 1130 |
rs367572240 | snp | C/G | 3.32984e-05 | 0.00408021 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715150 | GTTGTTGTTGTTGTT[C/G]TTGTTTCTGATGACC | 1130 |
rs367575741 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LYST | GRCh38.p7 | 1:235864711 | CCAAGGTGGATGGAT[C/T]GCTTGAGCCCAGGAG | 1130 |
rs367575862 | snp | C/T | 1.68633e-05 | 0.00290368 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762851 | TGAAAGATCTTGCCA[C/T]CTAGAATCCAAATTT | 1130 |
rs367594482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850234 | CCAAATACCTACAGC[C/T]AACTGATCTTTGACA | 1130 |
rs367601517 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235778068 | GCTAGGACTACAGGC[A/C]CCTGCCACCACACCC | 1130 |
rs367606043 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790629 | TGCATCTCCATGTAC[A/G]TATAAAACCCTAAAC | 1130 |
rs367617394 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689128 | AAATGTATCTCTAGA[C/T]GAAAATGCAATATAG | 1130 |
rs367688184 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808488 | GGCAGAGTTTTTACA[C/T]AAATCTGAAGCACGT | 1130 |
rs367699240 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235817225 | AAAAGAAAAAAAAAA[-/A]CATGCTGGTGAGGTT | 1130 |
rs367716348 | in-del | -/ATTT | | | intron-variant | LYST | GRCh38.p7 | 1:235680954 | GAGGGCAACCCATAC[-/ATTT]ATTTATTCATCCAAC | 1130 |
rs367717648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779797 | TCAACAACAACAACA[A/C]CACCACAAACAACAA | 1130 |
rs367736258 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235748991 | TCAACAAATGCTAAA[A/T]GAATCTATTTAGGAA | 1130 |
rs367748112 | snp | G/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792090 | CATAGTAGTATCACT[G/T]TCAATAATTTTCAGA | 1130 |
rs367765539 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764650 | GATTACAGGCATGTG[C/T]CACCATGCCAGGCTA | 1130 |
rs367772182 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732328 | TTTCTTTTTTGACAG[G/T]GTCTCATTCTGTTGC | 1130 |
rs367791091 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235678754 | GTCAGAAGTTACTAC[C/T]AGCCTAAATTTTGTA | 1130 |
rs367792096 | snp | C/T | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235729649 | ACACTGATGCATCTT[C/T]GATTCACTCTGTCAA | 1130 |
rs367803787 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235700291 | CCATCAGAGTGAACA[A/G]GCAACCTATAGAATG | 1130 |
rs367834781 | snp | C/T | 1.65935e-05 | 0.00288036 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777092 | AAACAAATATGCCAG[C/T]TCCACCAATTTCGTG | 1130 |
rs367847122 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805931 | TTATGGAAGAAATAT[A/G]CTGTAACTCTAATTT | 1130 |
rs367856185 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235755213 | GCCAACATGGTGAAA[A/C]CCCATCTCTACTAAA | 1130 |
rs367867898 | snp | C/G | 3.30693e-05 | 0.00406615 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809506 | TAAATCCATGATGCT[C/G]AATGAATTCTTGAAC | 1130 |
rs367891645 | snp | A/G | 1.66696e-05 | 0.00288696 | intron-variant | LYST | GRCh38.p7 | 1:235758952 | AAAGGTGGGAGGAGT[A/G]TACAAAAACACATAA | 1130 |
rs367940571 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235816746 | ACAGAATAAAGAGCC[C/T]AGAAATAAAGCTGCA | 1130 |
rs367944585 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785177 | GCAAATTCCATCTCC[C/T]CCTTCAGGTCTCAGG | 1130 |
rs367994802 | in-del | -/TTATT | | | intron-variant | LYST | GRCh38.p7 | 1:235767635 | CACTGGTATTCTATT[-/TTATT]ATTTTTTTAATCCCT | 1130 |
rs367995708 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703338 | TACAATGCTGGTAGA[C/T]AGTTGAAGAGATAAT | 1130 |
rs368003185 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235850800 | CACTAATGATCAGGG[A/G]AATGCAAATCAAAAC | 1130 |
rs368003763 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708266 | CTTTAAAATTTCTCC[C/T]TGTTGCTAGTCTGTA | 1130 |
rs368038754 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235742716 | ATAAATAAGCCTACA[A/C]TGATTTTGCAATAAA | 1130 |
rs368046320 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235764495 | CTTTTTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 1130 |
rs368052236 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235849769 | CAACCCCTTTTACAA[A/T]AGCTCCAAAAAAAAA | 1130 |
rs368074318 | snp | C/T | 6.63295e-05 | 0.0057585 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788774 | ATCCCAGTGAAATTA[C/T]ATGAATACATCCTTC | 1130 |
rs368095341 | snp | C/T | 6.59424e-05 | 0.00574168 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830269 | AGTAATAGAAATCCT[C/T]GACCATGGACAAGGT | 1130 |
rs368106433 | snp | C/G | 1.66582e-05 | 0.00288597 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744003 | TTTGAATCCTTCTAC[C/G]AGATATGTAAAAATT | 1130 |
rs368119710 | snp | A/G | 4.96816e-05 | 0.00498381 | missense, stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766105 | GAAAAGTAGAAGTTC[A/G]TGGGATTGTGACAAA | 1130 |
rs368135807 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873699 | AGCCAGTATTTGTCT[A/G]TCTTAATTCCCAATA | 1130 |
rs368143986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852608 | TGGAACACAGTCATA[C/T]GTAAGACGTAACTGC | 1130 |
rs368191555 | snp | A/G | 0.000142389 | 0.00843649 | intron-variant | LYST | GRCh38.p7 | 1:235777319 | CTTTCCTGAAATACA[A/G]ATATTTTCATTCAGT | 1130 |
rs368198151 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235818026 | TTATACACACATGTC[A/G]ATTTTGCAATGTACA | 1130 |
rs368218330 | snp | C/T | 4.97558e-05 | 0.00498753 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809832 | AGATGCAACACTGTT[C/T]GAAAGAGCATCCTTT | 1130 |
rs368225228 | snp | A/G | 1.65053e-05 | 0.0028727 | intron-variant | LYST | GRCh38.p7 | 1:235730982 | TATCTTTATCTAATG[A/G]CCATAGTTCTCTGCT | 1130 |
rs368254612 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878214 | GGAGCAGGTGAGCTC[A/G]GCCTTCAGCTGGAGG | 1130 |
rs368254676 | snp | C/T | 1.65356e-05 | 0.00287533 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802969 | TTCGTAACCTTCTTC[C/T]TCAACTAAAAGTTTA | 1130 |
rs368264952 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768405 | TCACAAATGAATGAA[A/T]CTGCCTTACATCCAA | 1130 |
rs368266268 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235742972 | CTTGTTTTACTATTA[C/T]TGTTAATCTCTTACT | 1130 |
rs368343984 | snp | C/T | 0.000428689 | 0.0146342 | synonymous-codon | LYST | GRCh38.p7 | 1:235677572 | GCTGGTTATCTCTTC[C/T]GTGTGACCATAGAGA | 1130 |
rs368344048 | snp | A/T | 1.67214e-05 | 0.00289144 | intron-variant | LYST | GRCh38.p7 | 1:235709047 | CTTAAAATATTCAGG[A/T]TCTATCTTATATAAA | 1130 |
rs368353301 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829139 | AACCCGGAGGTGGAG[G/T]TTGCAGTCAGCCGAG | 1130 |
rs368389381 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738918 | AAGGTGACTCTGACT[A/C/T]CTGAGGAAGGGGCCC | 1130 |
rs368394921 | snp | A/G | 4.97261e-05 | 0.00498604 | synonymous-codon | LYST | GRCh38.p7 | 1:235664584 | TCCAACGAGATCCCC[A/G]TTCACCGTCCAGAGT | 1130 |
rs368394997 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235689815 | TATCCCAATAAAGCT[A/C]GAAAAAAATAAAAAT | 1130 |
rs368397841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706927 | ACTACTGGCCTAAAT[A/G]AGCTCAGATATGGAG | 1130 |
rs368404609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235706247 | TGAGGAACAGCATGT[A/G]CACGAAGGACTTTTT | 1130 |
rs368408915 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685538 | GAGTTCAAAAGGGAA[C/T]AAGCTTGGAAAAAAA | 1130 |
rs368465866 | in-del | -/TCAATCAA | | | intron-variant | LYST | GRCh38.p7 | 1:235701645 | CAATCAATCAATCAA[-/TCAATCAA]GTGACAGATTGTAGT | 1130 |
rs368491155 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235878918 | ATTTAGGGGTGCAAG[G/T]GCAATTGTATTACAT | 1130 |
rs368492988 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235692385 | CTGCTATCAGTCTGA[A/C]TCTTTTTTTTTTAAG | 1130 |
rs368494621 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665152 | GCGAAAAAATAAAAA[G/T]AAGAAGAAGCAATCT | 1130 |
rs368500877 | snp | A/G | 0.00013212 | 0.00812666 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746446 | ATTCTCCGTTGCATC[A/G]TCACATGAAGCTCAT | 1130 |
rs368551452 | in-del | -/CTGAACTCAT | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235804377 | AGGAGATAAGATCCA[-/CTGAACTCAT]CTGACCAAGTCCTAG | 1130 |
rs368559915 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235691581 | ATGCCCTTCACTGAT[A/G]TTGAGCAGGAGATTT | 1130 |
rs368562685 | snp | A/G | 8.23608e-05 | 0.00641667 | missense | LYST | GRCh38.p7 | 1:235686950 | AGCCCAGAACCTACC[A/G]TGCTGCTTGTAAATC | 1130 |
rs368568991 | snp | A/G | 1.65176e-05 | 0.00287376 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757446 | TATAGGTACCAAACA[A/G]TCTTCAGTTACACTA | 1130 |
rs368572209 | snp | C/T | 0.000100097 | 0.00707378 | intron-variant | LYST | GRCh38.p7 | 1:235788875 | TGTTAGAATGATCAG[C/T]AAAATGGTTCGTAAC | 1130 |
rs368573685 | snp | C/T | 0.000115861 | 0.00761034 | missense | LYST | GRCh38.p7 | 1:235712143 | TCAAAAGATGAGAGT[C/T]GCCAAGTTGTATTTG | 1130 |
rs368577876 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884540 | CACCTGGCCCACAAT[A/G]TGAGTTTGAAGCATG | 1130 |
rs368583893 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763099 | TTAATTCCAACTGTA[C/T]TTATAGTTATTTCTA | 1130 |
rs368585550 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864396 | CTCAGTAAACAAGTA[C/T]CCCATCTTTCTACTT | 1130 |
rs368594342 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736512 | GGATGTGAAGAGGTT[C/G]CAAGACACAAAGATA | 1130 |
rs368594555 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235784838 | AACAAATTTGCTGAT[C/T]GGCTACAGCTGCCAT | 1130 |
rs368605567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235680660 | CTGGAGTGCAATGGC[A/G]CAACCTTGGCCCACT | 1130 |
rs368618083 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | LYST | GRCh38.p7 | 1:235664022 | GGGAAATGTAATTTC[C/T]CTCACAGGCTTTAAG | 1130 |
rs368638396 | in-del | -/ACTTCTTTACAGTGACTA | | | intron-variant | LYST | GRCh38.p7 | 1:235841089 | TTAGGCCAGTGACTA[-/ACTTCTTTACAGTGACTA]CTGAGACTAAATCCA | 1130 |
rs368661929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235815858 | TAAAATGGGGCCGGG[C/T]GCGGTGGCTCACGCC | 1130 |
rs368669708 | snp | C/G/T | 7.09704e-05 | 0.00595659 | intron-variant | LYST | GRCh38.p7 | 1:235746537 | GAGGACCTTTAAAAG[C/G/T]ATATAAATTAAAACA | 1130 |
rs368677394 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | LYST | GRCh38.p7 | 1:235791689 | AAATCAGATAATCCT[A/G]TCATCATACCTGTAC | 1130 |
rs368682879 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235754648 | TGAACTATAAAGGAT[A/G]AAGTTATATTAGAAA | 1130 |
rs368698157 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235782180 | TAACAATGGGGAATT[-/C]TTTTTTTTTTTTTTT | 1130 |
rs368738466 | snp | C/G/T | 5.03267e-05 | 0.00501606 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774969 | ACACCTGATGAATCA[C/G/T]AGAAAGTCCATTACA | 1130 |
rs368740409 | snp | C/T | 0.000147743 | 0.00859359 | synonymous-codon | LYST | GRCh38.p7 | 1:235712178 | ATGAAAAGTTCTGTC[C/T]GGAATGTCAAAACTT | 1130 |
rs368762915 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874816 | GTTGTTTTGTTGGTG[G/T]TGTTGATATGGTTGT | 1130 |
rs368765786 | snp | A/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826787 | CCCAGGCTCAAGCAA[A/T]CCTCTCACCTCAGCC | 1130 |
rs368771903 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235776935 | CATTTTAATATGTAA[-/T]TTTTTTATGTTAAAA | 1130 |
rs368784093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721670 | TTGTGGAATAGGCAA[A/G]ACCACAGAGAATAGA | 1130 |
rs368792705 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235801221 | CTTACAAAACCTTTT[C/T]CAATCTTTTCCTATA | 1130 |
rs368811484 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665138 | AGAGACAATAACCAG[C/T]GAAAAAATAAAAATA | 1130 |
rs368828427 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235768084 | TCTCACTACGTTTCT[-/CT]GTCTTGGAGTGCTTC | 1130 |
rs368829690 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235794250 | TATATCATAAAATAG[A/T]CTGCTATCTTATCTT | 1130 |
rs368836614 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235716455 | GGAATGTGACTACTA[A/C]ATACTGGAATAAACA | 1130 |
rs368845809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737646 | GAAAAAGGCCATGTC[A/G]ACACAACAACTTGAA | 1130 |
rs368850112 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842249 | GAAAATAAATGTTGA[C/T]AGACAAGCAGAAAAT | 1130 |
rs368856298 | in-del | -/GTCT | | | intron-variant | LYST | GRCh38.p7 | 1:235666019 | AGAGGCTTTGCTTCT[-/GTCT]TTTATTAAGACAATG | 1130 |
rs368858289 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235784625 | CTCAGTTGCCTCATA[C/G/T]GTAAAATTGGGATAA | 1130 |
rs368865010 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235840562 | TAATCTGCTAAACCC[A/G]CAGCAAGACCTAAAC | 1130 |
rs368865603 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235721976 | AGGTAAGGGGTGCTT[C/G]GTGGAGAGGGAGGGG | 1130 |
rs368868854 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720759 | ATCATTGAAGGATCG[C/G]CCAGCATGTTTGTTT | 1130 |
rs368881198 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235782243 | GCACGATCTCAGCTC[A/G]CTGCAAGCTCCGCCT | 1130 |
rs368896842 | snp | A/T | 1.66261e-05 | 0.00288319 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808796 | GGGCAGGATCCCTTG[A/T]AATCTGTAAGAAGGA | 1130 |
rs368896974 | snp | A/G | 3.29777e-05 | 0.00406051 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728077 | AAGCCTCTACTCACC[A/G]AACTTTCAACTGTAT | 1130 |
rs368906017 | snp | C/T | 1.71779e-05 | 0.00293064 | intron-variant | LYST | GRCh38.p7 | 1:235810576 | GAATACCTCAATATG[C/T]TTTAAAACTCAATTT | 1130 |
rs368942399 | snp | C/T | 0.000353864 | 0.0132969 | intron-variant | LYST | GRCh38.p7 | 1:235830468 | GATTAGGAAAACAAA[C/T]ACAAATTTACTTTTA | 1130 |
rs368951917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235719197 | CAAATTTTGTATTTT[C/T]AATAGAGTTAGGGTT | 1130 |
rs368963679 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702620 | GCTTTCGCTGCTGCA[C/T]CTGTCTTGCACTGAC | 1130 |
rs368985090 | snp | G/T | 1.71885e-05 | 0.00293154 | intron-variant | LYST | GRCh38.p7 | 1:235663115 | CATTTGTACATTATA[G/T]TTCTTAAAAGTGTAT | 1130 |
rs368990884 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870960 | GGAATACAAGACTGC[A/G]ATTTCAGCAATAGTA | 1130 |
rs369001190 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235847543 | GAATGGAACCATACC[A/G]CACATTTCAATGCTA | 1130 |
rs369008939 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235752530 | CTAAGGATGAAGATT[A/G]TGTGGGTATGAACAG | 1130 |
rs369009087 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | LYST | GRCh38.p7 | 1:235831193 | TTAAGTTAAATAAGA[-/C]CATGTATTGCCTCAC | 1130 |
rs369034545 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235698790 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGCA | 1130 |
rs369043065 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770162 | ACATGAAAAGTACCT[C/G]CAAAACCTGACAAGT | 1130 |
rs369049418 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235666199 | ATGTCTATCAACAGA[C/T]GCATAAACAAAATGC | 1130 |
rs369059599 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235858523 | CTCACATCTATGTGC[A/C]AATTTTTCCATCTCT | 1130 |
rs369092813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737502 | ACTATCATCTCCTTA[A/T]AAGGATATAAGGTCT | 1130 |
rs369118576 | snp | C/T | 6.60698e-05 | 0.00574722 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810064 | AGTCAAATGGAGAAT[C/T]GTTCATGTTACTGAT | 1130 |
rs369145577 | snp | C/T | 4.98492e-05 | 0.00499221 | intron-variant | LYST | GRCh38.p7 | 1:235751406 | CAAGCTATGTGGTTA[C/T]TAATTTTTTAATTGA | 1130 |
rs369150442 | in-del | -/AAATTGCAGGTGCCCC | | | intron-variant | LYST | GRCh38.p7 | 1:235711269 | CAAGGCAGGTGCCCC[-/AAATTGCAGGTGCCCC]AAATTGCAGGTGCTG | 1130 |
rs369153654 | snp | C/T | 0.000366124 | 0.0135251 | intron-variant | LYST | GRCh38.p7 | 1:235800312 | TGTTTAAAACAGTTT[C/T]AACTTACCTTGAAAA | 1130 |
rs369155467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786497 | ACAGTGTGGTGATTC[C/T]TCAAGGATCTGGAAC | 1130 |
rs369160076 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235790032 | ATATTCTTTATCTCT[-/CT]TCAAAACTTTTTATA | 1130 |
rs369163337 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant | LYST | GRCh38.p7 | 1:235728176 | TAAAATGTATGTGCA[C/T]ACTACCATTCATGGT | 1130 |
rs369191840 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687877 | CAGGCTTCCTCAGAA[A/G]CCTTGTTTTCTTTTT | 1130 |
rs369196159 | in-del | -/GAGCA | | | intron-variant | LYST | GRCh38.p7 | 1:235705647 | TGCCTCAGTCTCCCA[-/GAGCA]TTTGGGTTATAGGCA | 1130 |
rs369200597 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235750401 | GAGTTTTTCACATGG[C/T]TTAAAATTTTTGCAT | 1130 |
rs369203478 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722709 | CAGGCTGGTCTTGAA[C/G]TCCTGACCTCATGAT | 1130 |
rs369207016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713914 | TGAATACATTCATAA[C/T]AGTAACATGAATAAA | 1130 |
rs369246831 | snp | A/T | 4.98923e-05 | 0.00499436 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744133 | TCTGGAGTTCTCAAA[A/T]TGTCAATAATGTCTG | 1130 |
rs369248827 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235744620 | GGAAAAAAAAAAATG[C/T]TGGGGACGATGGCTC | 1130 |
rs369258873 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235686092 | CAAAAACAGGCCGGG[C/T]GTGATGGCTCACACC | 1130 |
rs369275639 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235880558 | ATTTATTCTAATGCT[A/G]TAACTGATACTGCCT | 1130 |
rs369298978 | snp | A/C | 1.68576e-05 | 0.00290319 | intron-variant | LYST | GRCh38.p7 | 1:235693339 | TAAATAAAATAAAAT[A/C]AAGTGTTTACCTGGT | 1130 |
rs369314866 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235823004 | GGAGCCAAAGTGGCT[-/A]ATTCCAGCTGAGCCA | 1130 |
rs369338837 | snp | A/G | 1.69896e-05 | 0.00291454 | intron-variant | LYST | GRCh38.p7 | 1:235810556 | GAATGAAAAAAGAAG[A/G]CTTAGAATACCTCAA | 1130 |
rs369369310 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235717455 | AGGAGAATGAATTCT[A/C]ATCCCTCCAGGAATG | 1130 |
rs369380517 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235839620 | CCAACACGGAGAACC[C/G]CCCCCACCACGCCCC | 1130 |
rs369410070 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235708547 | AATGCAGTTTATACC[A/G]AACACCTGCTTTCCT | 1130 |
rs369422081 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765435 | CTCAAAACAAACAAA[C/T]AAAACCCTTTCAATG | 1130 |
rs369436249 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235699639 | TCTGGTTCTAGATCC[C/T]TGAGGAATTGCCACA | 1130 |
rs369438958 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235803882 | ATCAAGGAGCTAAAA[C/G]GAGAAGTTATATAAA | 1130 |
rs369441220 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235882705 | AATATAACAGAGGCT[A/G]AAGGGTTAGGGAGGG | 1130 |
rs369455929 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235771802 | TTGCCTCTTCATGTA[A/C]CAACAATTTTGTAAT | 1130 |
rs369474434 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235879985 | CAGGTGATCTGCCCA[A/C/T]CTCAGCCTCCCAAAG | 1130 |
rs369484787 | snp | C/T | 0.000131954 | 0.00812156 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733835 | AAAATCTTACCTTTG[C/T]TGATTATTGTTAACT | 1130 |
rs369493781 | snp | C/G | 2.22413e-05 | 0.00333469 | intron-variant | LYST | GRCh38.p7 | 1:235782100 | TTCCTACATTAAAAA[C/G]AAAACAAAGTTAAAG | 1130 |
rs369494275 | snp | A/G | 3.32452e-05 | 0.00407695 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810485 | TCTTTGTGAACTTGA[A/G]TTCTTTTCTTTGGTC | 1130 |
rs369502347 | snp | C/T | 0.000131903 | 0.00811999 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806002 | GATGGTATGGGGTCA[C/T]TTTTTATAGCCAAAG | 1130 |
rs369518056 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235780344 | AGGAGTTCAAGGCTG[C/T]GGTGAGCCATGATCA | 1130 |
rs369555253 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | LYST | GRCh38.p7 | 1:235729853 | GAGAAATGACTGAAA[C/T]GCCTAGAAAAGGCTA | 1130 |
rs369578040 | snp | A/C/G | 9.80498e-05 | 0.00700109 | intron-variant | LYST | GRCh38.p7 | 1:235774881 | GTATCACTGCATATG[A/C/G]AACTATAAGAATAAA | 1130 |
rs369592090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796129 | TTGGGAGGCTCAAGA[C/T]AACAATTAGAATACA | 1130 |
rs369600279 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738804 | ATGAAGAATCTTAGG[C/T]GGGTGCACCCAATTT | 1130 |
rs369631685 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859721 | TCCCTCTCCTTTATC[C/T]ATAACTACACAAGGC | 1130 |
rs369646020 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235850265 | AAGCAAACAAAAACA[-/TA]AAGTGGGGAAAGGAC | 1130 |
rs369647943 | snp | A/G | 1.66054e-05 | 0.00288139 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766213 | CCAAGGACTTCTGCT[A/G]TAATTTTCACAAATG | 1130 |
rs369670504 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235858067 | AGAAGCTATATATTC[C/T]GGGGACTTCATTATC | 1130 |
rs369676722 | snp | C/T | 8.31276e-05 | 0.00644646 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808671 | TTCTGGATTAAATTG[C/T]AAATGTGATTTGCAA | 1130 |
rs369683015 | snp | A/G | 8.29291e-05 | 0.00643876 | intron-variant | LYST | GRCh38.p7 | 1:235716679 | AAAACACAATTTTTC[A/G]TTTAATAAAGTACGA | 1130 |
rs369723811 | snp | C/G/T | 8.74369e-05 | 0.00661148 | intron-variant | LYST | GRCh38.p7 | 1:235752185 | TGCTAAAGATAACAA[C/G/T]AAAAGAAGAAAACAG | 1130 |
rs369729439 | snp | A/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853767 | CAGGAAATAAAGGAA[A/T]CTCAGGCATAGGGCA | 1130 |
rs369738846 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689035 | TAATAATAACAACAA[C/T]AACAACAACAACAAT | 1130 |
rs369760460 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813158 | AAAAAATCCTTTTTC[C/T]TGAAAGTCTGCATTT | 1130 |
rs369763211 | snp | A/G | 3.30251e-05 | 0.00406343 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759091 | AACAGCTGCAGATCC[A/G]TTCTGTGAAGGAAAA | 1130 |
rs369772005 | snp | A/G | 6.60197e-05 | 0.00574504 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806380 | TCTGAGTCATTGGCC[A/G]ACTCCCTGTCAGACT | 1130 |
rs369775104 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | LYST | GRCh38.p7 | 1:235728009 | CCTTCTCTCTAGTTA[C/T]ACTGAATTGATACAT | 1130 |
rs369806395 | in-del | -/A/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235849775 | TTTTACAATAGCTCC[-/A/AA]AAAAAAAAAAAAAAA | 1130 |
rs369806680 | snp | A/G | 5.02626e-05 | 0.00501286 | intron-variant | LYST | GRCh38.p7 | 1:235724206 | GAAATAGGCAAAAAT[A/G]TTTGTTTTACCGGAA | 1130 |
rs369825666 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846478 | CTCTTCAACACCCCC[C/T]CAAAATTTCTCTAGT | 1130 |
rs369831783 | in-del | -/TAT | | | intron-variant | LYST | GRCh38.p7 | 1:235705743 | AAGATGGTTCAGGAT[-/TAT]AAACAAAAAGGGTAT | 1130 |
rs369838675 | snp | A/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751043 | CAAGAAATAACTGAA[A/T]GAGAAAAGCACTAAA | 1130 |
rs369847228 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693106 | AGATAACAAGGTCAG[A/G]AGATCGAGACCATCC | 1130 |
rs369847918 | snp | A/C/T | 5.20883e-05 | 0.00510308 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780926 | CTGATTTGTTCACAT[A/C/T]GCAAAATTTCTTTAT | 1130 |
rs369989147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727403 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 1130 |
rs369994212 | in-del | -/ATATCT | | | intron-variant | LYST | GRCh38.p7 | 1:235756062 | tctatatctatatct[-/ATATCT]gtatctatatctatc | 1130 |
rs370014429 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235869999 | CTCCACGTCTTTGCT[A/C]AAATTTCACCTCTCA | 1130 |
rs370022285 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819183 | TAGCACTGGGGGAAA[C/T]GAGTCTTTCCTTCAC | 1130 |
rs370022675 | snp | A/G/T | 1.65987e-05 | 0.00288082 | LYST | 1 | allele_origin=G(germline)/A(germline) | 1:235809893 | CTGCAGAAACTACTC[A/G/T]ACTCTCCAAGTTGTC | 1130 |
rs370022941 | snp | A/C/G | 1.65954e-05 | 0.00288053 | synonymous-codon, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781942 | CGTTGAAGAGAAGCA[A/C/G]ATTTCCCAGGTCCCA | 1130 |
rs370036687 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235709739 | ATTTTAATAAATTTA[A/T]GATTATATTTAGTAA | 1130 |
rs370037768 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731154 | CATGAGGTTGGATAG[C/T]AGATGGGGTCATACC | 1130 |
rs370039781 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714833 | TGCAATAATGTACAT[A/G]GGCTCCAAAGGTAAC | 1130 |
rs370042884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756486 | CTTTATATACTATAT[C/T]GCAACTAGCTCAGGG | 1130 |
rs370066009 | snp | A/G | 8.24667e-05 | 0.00642079 | intron-variant | LYST | GRCh38.p7 | 1:235677060 | GTTAGAGCACCAGCC[A/G]GCCCTGTGCTTTGGG | 1130 |
rs370070995 | snp | C/T | 0.000115616 | 0.00760226 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753246 | ACTTCTGAAACAATC[C/T]CATGTTTCTCACATC | 1130 |
rs370072868 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235772032 | GTTTGAGACCAGCCT[A/G]GGCAATATAGTGAGA | 1130 |
rs370073655 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235741747 | CAGATTGGTTTTAAT[A/T]GTCAAAATTAGAAAG | 1130 |
rs370081869 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235684122 | TGTGTCATGACCTCA[A/G]AACTAAAAGAAATGT | 1130 |
rs370103719 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235755433 | GAAAAGAAAAGAAAA[A/G]AGACAAAAGATTCCC | 1130 |
rs370113456 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235798877 | CTAAAGGGTACAGGG[C/T]TTCTTTTGGGGGTGA | 1130 |
rs370124279 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867358 | TCTAGAGGATGAAGA[C/T]AGAAGAAATAACGGG | 1130 |
rs370150457 | snp | C/T | 1.66214e-05 | 0.00288278 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788751 | CACTTGGATCATCAA[C/T]GCTTTGGATCCCAGT | 1130 |
rs370173269 | snp | C/T | 8.23839e-05 | 0.00641757 | missense | LYST | GRCh38.p7 | 1:235662992 | ATTGGCTGTTTCAAG[C/T]GCTGCTGGTCCTTCC | 1130 |
rs370213093 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746738 | TTTCAAAGTCCTAAA[C/T]AACAATGTTGAAGCT | 1130 |
rs370217183 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235785815 | TTCAATACAATACTT[C/G]CCAATGCTTACAAAT | 1130 |
rs370229155 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759294 | TTGGGACATCACTGA[C/T]AGAGACCTGGGCTGA | 1130 |
rs370248017 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235861335 | TTAGGTAAGATTTTT[A/G]TTTTTCAGCAGTTAG | 1130 |
rs370263812 | in-del | -/C | 0.0115703 | 0.0751748 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853115 | ACTTCTTGCCCCCCC[-/C]ACAAACTTCTCAAGA | 1130 |
rs370267512 | snp | C/T | 1.78694e-05 | 0.00298905 | intron-variant | LYST | GRCh38.p7 | 1:235755683 | AATTTAGATAATGCA[C/T]TAAAATTAAATATAA | 1130 |
rs370273558 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235747095 | ATTTGGAATTCAATG[C/T]TACAAAAGCATTTCC | 1130 |
rs370278659 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235877775 | TGCATCGCTTAGCAG[C/T]GTAGATGTAGCCCAG | 1130 |
rs370286801 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235803104 | TTGTAACATTTGCTT[C/G]TTTTTAGTAATAGAA | 1130 |
rs370292911 | snp | A/T | 1.67629e-05 | 0.00289503 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774972 | CCTGATGAATCATAG[A/T]AAGTCCATTACAATT | 1130 |
rs370293573 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831028 | CAAACAGAATAGGGG[A/G]ACATAAATACAGAGG | 1130 |
rs370295550 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235856072 | ATAAATATTTTCTGA[A/G]CACAGGCATTTCAAA | 1130 |
rs370339994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851975 | CACCATACTTCGTGG[C/T]ATGTTCAACTTTCAT | 1130 |
rs370344580 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235791549 | ACAACTCATGCTTTG[A/G]TAAGTCAGGACCTAC | 1130 |
rs370355370 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662286 | CTGTATTCTTGTTTG[C/T]GGCTGTCAAAAAAAT | 1130 |
rs370361870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732865 | ATTTGCTGAAAATAT[A/G]TTTCCAGGCTTTTTT | 1130 |
rs370381486 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235816363 | GAGAATCACTTGAAC[C/G]TGAGAGGCGGAGGTT | 1130 |
rs370384426 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687660 | TTCCATGCTAGCTGA[C/T]CCCCACCCTGAGCAC | 1130 |
rs370422240 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746474 | CATCATTTGCCACTG[A/G]ACGCATTTTCATCAG | 1130 |
rs370433232 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806679 | TATCAGAGTTTCAAA[C/T]GCTTTTAGAGAATGA | 1130 |
rs370438210 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235870542 | ATTCACGAATTGTTT[C/T]GTGCTCAATTAAACT | 1130 |
rs370440637 | snp | A/G | 1.68168e-05 | 0.00289967 | intron-variant | LYST | GRCh38.p7 | 1:235802872 | TTAATGATCTGGCTT[A/G]CAGATCTAATTACAA | 1130 |
rs370441301 | snp | C/T | 0.000115744 | 0.00760647 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773907 | TAACATCTTGGATTA[C/T]AGCATTAGAGTCTAC | 1130 |
rs370447638 | snp | C/T | 1.65938e-05 | 0.00288039 | intron-variant | LYST | GRCh38.p7 | 1:235677206 | GAAAGAAAAAAGACA[C/T]GAATTTGTATATGAT | 1130 |
rs370451935 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884153 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 1130 |
rs370472890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235774364 | GGGGTGGAGGCAAGG[A/G]TAGAGCAATCGTCTT | 1130 |
rs370519849 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883386 | CATTGAGGAACACAC[A/G]CGGTTGAGTCAAACA | 1130 |
rs370542590 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235842231 | GAAAAAGAAAGAGGC[C/G]AGGAAAATAAATGTT | 1130 |
rs370547926 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235856500 | TGGGTTGTGAACTTT[A/T]ATGAGAGTACAACAT | 1130 |
rs370548588 | snp | C/T | 1.64904e-05 | 0.00287139 | intron-variant | LYST | GRCh38.p7 | 1:235702724 | AGGTTTTGCTGCACT[C/T]GATTGAAATCCAAAT | 1130 |
rs370563833 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724138 | CTTTAATTTCTTCAT[A/G]TGTCCAGGAAAATGA | 1130 |
rs370569582 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235685110 | TGTGTAAACTATTTC[C/T]TCTGCCTGAAATGTT | 1130 |
rs370575701 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718225 | ACAAGCTATGTTAAT[A/G]GTTGTAGCTGAAAAA | 1130 |
rs370586190 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878092 | GTCTGGGCCCACTTA[A/G]TAATGTAATCTTCTG | 1130 |
rs370607227 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235748084 | ATAAAATAAAATAAT[C/G]AATATAAAACATAAT | 1130 |
rs370677118 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235783614 | GTAACAAACCTGCAC[A/G]TTCTGCACATGTATC | 1130 |
rs370681138 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235729965 | AAGCAAACATTGTTT[C/T]ATGCCTCTGATACTT | 1130 |
rs370683101 | snp | C/T | 1.6522e-05 | 0.00287414 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809020 | TCAGTGCTGGCAATT[C/T]AAAAGCATGGAGCAA | 1130 |
rs370700437 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806695 | GCTTTTAGAGAATGA[A/C]TTCGAATACCATTTA | 1130 |
rs370702570 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720868 | AGAAGATTAGGGAGG[C/T]TATTTGTGAGTATAT | 1130 |
rs370714287 | in-del | -/GTAA | | | intron-variant | LYST | GRCh38.p7 | 1:235697364 | ACAAAGTAAGAGAAA[-/GTAA]TATGGATTATAAGCT | 1130 |
rs370725333 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755526 | ATTTCGATGAAGCAT[C/T]CTAACAATTCTTGAG | 1130 |
rs370740776 | snp | A/C | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808370 | AAATGCATACAATTT[A/C]TCACTCACTTGAAAG | 1130 |
rs370744420 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235836698 | TTCCCCTGAAACCAT[C/T]TCTCCCCAAGAATGC | 1130 |
rs370775296 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884418 | TGAGCCACCGCGCCC[A/G]GCGCCCAGCTAATTT | 1130 |
rs370793336 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235843533 | TGTTGACAAATTTTA[C/T]AGCTCTATGTAAATG | 1130 |
rs370812766 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761978 | GGGCCTGTTGTCGGG[A/T]GGGGGGAGGGGGGAG | 1130 |
rs370819416 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235849744 | AAGTGGAGAATCAAA[A/T]AAAAGAACTCAACCC | 1130 |
rs370845049 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235857008 | TGGAATGCAGTGGTG[C/T]GATCTCGGCTCACTG | 1130 |
rs370851980 | in-del | -/AAGTT | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235837651 | AAAAAGAATTCTGAG[-/AAGTT]AAGTTAAGTAAGATG | 1130 |
rs370862028 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702838 | AGCTCTCCTTCAATA[C/T]TGAGCTTGGCTCCAG | 1130 |
rs370862845 | snp | C/T | 3.36547e-05 | 0.00410198 | intron-variant | LYST | GRCh38.p7 | 1:235830174 | AAAACCATGTAGCTA[C/T]AGTTAACTATCATAT | 1130 |
rs370867099 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235754470 | CCTCAGGTGATCCAC[C/T]TGCCTCTGCCTCCCA | 1130 |
rs370871996 | snp | C/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695789 | AGGAGCCCGCCACCA[C/G/T]GCCCGGCTAATTTTT | 1130 |
rs370884855 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235742741 | AATAAAAAAGAGAAA[G/T]GATTCATAATAAAGA | 1130 |
rs370898869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702354 | CAATCCTTTTGATTG[C/T]AGATGATAACCAAGA | 1130 |
rs370958080 | snp | G/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809837 | CAACACTGTTCGAAA[G/T]AGCATCCTTTGAATC | 1130 |
rs370969370 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235758418 | GTATTGCTTTCTGAG[A/G]CCATTTTAGCTTTCT | 1130 |
rs370983097 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235669882 | ACAACTTGCAGTCAA[C/T]ACCCTCTACCAGTGA | 1130 |
rs370988137 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235689429 | TGATCCTGCTCCTAT[A/G]TGGAATCTAAAAAAA | 1130 |
rs370995142 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | LYST | GRCh38.p7 | 1:235728048 | TCTGTCTAGATTTAT[A/G]TAAATACAGACTTAA | 1130 |
rs371002603 | snp | C/T | 1.72344e-05 | 0.00293546 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774929 | TTCAAAATGTAAAAC[C/T]CAACAATGCATTTTT | 1130 |
rs371004069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235694524 | CTTTATTTATTCCAG[C/T]ACCTAGCAGAATACC | 1130 |
rs371026680 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235754747 | TGACCAAAAGATTTC[A/C/G]TTAAGAGTGAGTTCA | 1130 |
rs371033041 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235798924 | TTAATTGTGGTCATG[A/G]TTGCACAGCTCTGTA | 1130 |
rs371040509 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787338 | ACCTGTGCTAGTAAA[A/G]CAGCTTTCATGTCAT | 1130 |
rs371097561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666737 | AAAGAAATAGAATTA[C/T]AGACAATATTTTCCA | 1130 |
rs371176284 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862506 | GATCTTAGAACATAT[C/T]TCCCCAAGGCCGGGT | 1130 |
rs371185792 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809298 | TGATGCATAAAATGA[A/G]AATATTCACATCGTC | 1130 |
rs371189535 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235872427 | AGCACTGTAGACATG[C/T]GATTGGACAAAAGAG | 1130 |
rs371193855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700523 | CAATAGTGAACTGAA[A/G]TTCACACAAGCATAC | 1130 |
rs371200923 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235683134 | GGTCCTAATAGTAGT[A/T]TTTGATAATTTTTTA | 1130 |
rs371222311 | in-del | -/TAAGT | | | intron-variant | LYST | GRCh38.p7 | 1:235837660 | TCTGAGAAGTTAAGT[-/TAAGT]AAGATGAAGACTGGG | 1130 |
rs371223456 | in-del | -/ACACACAC | | | intron-variant | LYST | GRCh38.p7 | 1:235666226 | ATGCAGTATGTACAT[-/ACACACAC]ACACACACACACACA | 1130 |
rs371243857 | snp | C/T | 1.66087e-05 | 0.00288168 | missense | LYST | GRCh38.p7 | 1:235709246 | GAGGATCATTACGCG[C/T]CCAAGGGGGAAGGTT | 1130 |
rs371248013 | snp | C/T | 0.00436225 | 0.0464983 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762757 | ACCAGATGGGCTTAT[C/T]ACCATAAATCCAGGG | 1130 |
rs371261339 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235834666 | AACCAGGCAGAAAAC[A/C]GCTGTGTTAGACAAT | 1130 |
rs371272509 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719399 | GGCTCACCTTGTCTA[C/T]TTTCTTCTAATAAAT | 1130 |
rs371278737 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235880284 | ATGTGAAAAAAACTC[A/G]GCAGGCTTGCCTTAT | 1130 |
rs371287070 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235834595 | AACTGTCTTAAGTTT[A/C]TTTCAGCTTGCCAAC | 1130 |
rs371332456 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854383 | ATACAAATTTCTATT[C/G]TCCAAAGCAGACATT | 1130 |
rs371403215 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235731828 | CTCCCAAAGTGTTGG[A/G]ATTACAGGCGTGAGC | 1130 |
rs371406880 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872517 | TCTTGGCATCTGTGT[A/G]CAGCATTCCTTCTTC | 1130 |
rs371426157 | snp | C/G/T | 3.46897e-05 | 0.00416457 | intron-variant | LYST | GRCh38.p7 | 1:235810586 | ATATGTTTTAAAACT[C/G/T]AATTTTAAGGTGACA | 1130 |
rs371441966 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235749861 | CTAAAGAGAGAGACT[A/G]AAGACTGCTAGAGAA | 1130 |
rs371442404 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734515 | TAAGGTCTGCTTTTG[C/T]TGATGCACTGGGAGG | 1130 |
rs371458292 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235723145 | TTGGCCTGGGCATTG[A/G]AAAGATGGAGTTGTC | 1130 |
rs371472084 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235715917 | CTCCTATCTTCCCAT[C/G]ATAAAGTAGGAAGTT | 1130 |
rs371476919 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813048 | GTCAGGAGTTCTTCT[C/T]TACATGTCAATGCCT | 1130 |
rs371524996 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235789038 | AAAAGCACGAGGGAT[A/G]AAAAATGGTAATTCA | 1130 |
rs371576746 | snp | A/G | 0.000115404 | 0.0075953 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805959 | TTTACCTAAACTGTC[A/G]GCACTCTTTTTTAGA | 1130 |
rs371593424 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235804476 | CTGGTCATACCCAAA[A/G]AACACAACTATATGT | 1130 |
rs371606214 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789030 | AACTCCAAAAAAGCA[C/T]GAGGGATGAAAAATG | 1130 |
rs371611162 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881660 | ATACACGTACATACA[C/T]ATATATATGCAATGG | 1130 |
rs371619029 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235834989 | GCGCGATCTCGGGTC[A/G]CTGCAACAACCTCTG | 1130 |
rs371647515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678805 | TTTATACTTCCATTA[C/T]GTTACTATAGCCATA | 1130 |
rs371705679 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712805 | GCATAGTCACTCTTT[C/T]GTTCATTTTTTTTCC | 1130 |
rs371728782 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788833 | TACTCTGCACCTTCT[A/G]GTCTGTCGCTCTCTA | 1130 |
rs371733219 | snp | C/T | 4.94352e-05 | 0.00497143 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751276 | ACTGGAGTGAATCTG[C/T]GAGGTTTTCAGAGTC | 1130 |
rs371736647 | snp | G/T | 5.04359e-05 | 0.00502149 | intron-variant | LYST | GRCh38.p7 | 1:235715389 | ATCCAGAGAATTCAT[G/T]ATTGTGGGCTCCAGG | 1130 |
rs371738691 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793554 | AAGGGTTAGCTCTTC[C/T]GAACATGTTCTTGAA | 1130 |
rs371795606 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235708386 | GTGTGCGGAAAAGAG[A/T]TAACATAGCAAGATT | 1130 |
rs371797959 | snp | A/G | 1.65386e-05 | 0.00287559 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744088 | GAAATTTCGGTCTGG[A/G]AAACTGAGGTCTTGC | 1130 |
rs371806766 | snp | A/G/T | 9.8931e-05 | 0.00703259 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715304 | GTGATAGGGCTGCAC[A/G/T]GGAGGCATGGGGTCA | 1130 |
rs371808058 | snp | A/G | 1.65031e-05 | 0.00287251 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808564 | CTGAAGTAACGCTTA[A/G]GTGTTGACAATGATG | 1130 |
rs371813222 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235680472 | TTGCTATGCTGCCCA[A/G]GCTGGTCTCAAACTC | 1130 |
rs371820210 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808700 | AATCTGTATACTATG[C/T]AATCTGTCTTCTTCA | 1130 |
rs371824226 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235720923 | AAAAGGGAAGGAGAA[G/T]AAAAAAACCCAGATA | 1130 |
rs371833566 | snp | A/C/G | 0.0001847 | 0.00960825 | intron-variant | LYST | GRCh38.p7 | 1:235806801 | AAAGCATGTAAAAAG[A/C/G]TTTAAATAAAGAAAC | 1130 |
rs371892925 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | LYST | GRCh38.p7 | 1:235764550 | TGTCACCCAGGCTGG[-/A]GTGCAATGGCACATT | 1130 |
rs371905334 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235742142 | TTATTTATTGGGCAC[A/G]GAGTTTCATTTGGGA | 1130 |
rs371940173 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731050 | CTGATTTCTGTCTAT[C/T]CCTAAGGAGATACTT | 1130 |
rs371950575 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869351 | GTGGCGGACGCCTGT[A/G]GTCTCAGCTAATCGA | 1130 |
rs371955503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235832373 | GAATAATTAAGTCTA[C/T]CTTCTAGAAATTAAG | 1130 |
rs371958764 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884214 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 1130 |
rs371962116 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845563 | AAAGCCCTTTTCTTT[C/T]GTAGCTGAGAGGTGG | 1130 |
rs371969130 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235768728 | AAAGACTGAATAAGA[A/G]TATCACATTGTCATA | 1130 |
rs371969301 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235743142 | CTACTCTATGGGTTT[A/G]CCATAGAGTATTCCC | 1130 |
rs371971029 | snp | A/C | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852967 | AGAATTCTACCTTTC[A/C]GAGCATTTTAGCGAT | 1130 |
rs371984606 | snp | A/C | 1.88973e-05 | 0.00307381 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780888 | GACCAATATCCACAT[A/C]TTTCTTGGTCATAAA | 1130 |
rs371984694 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235685565 | AAAAAGTAAGAACCT[A/G]GCTGGGCACAGTGGC | 1130 |
rs371992296 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235734881 | GATGTAATAATGTTA[C/T]GTTACATAGGAAAAC | 1130 |
rs372000599 | snp | C/T | 0.000181607 | 0.00952734 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757358 | CTTGAATAAGCTTGT[C/T]CATCACATCTTCAAG | 1130 |
rs372008303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818680 | GGCATATCTTTCCGG[C/T]AGAGTCCTCCTAATC | 1130 |
rs372017169 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857717 | TATACACACACACAC[A/G]TATATATACACAAAC | 1130 |
rs372034762 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715261 | GGAAGTGAAGCACAG[C/T]GCCGCTATTGGAATA | 1130 |
rs372035051 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | LYST | GRCh38.p7 | 1:235746576 | CAGTGTTAATAAGGA[C/T]CAAGGAAACTATTTT | 1130 |
rs372075872 | snp | A/G/T | 0.000216129 | 0.0103935 | intron-variant | LYST | GRCh38.p7 | 1:235758964 | AGTGTACAAAAACAC[A/G/T]TAAGTACCTGTGAGC | 1130 |
rs372095923 | snp | A/G | 1.65872e-05 | 0.00287981 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809748 | TTTAAAGCTGCTCTA[A/G]GCAATTCAGTTAAAT | 1130 |
rs372146426 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817517 | GGCACATATACATCA[A/T]GAAATACTGTGCAGC | 1130 |
rs372196915 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235839275 | TACAGTTTTTTTTTT[G/T]AGACAGAATCTCGCT | 1130 |
rs372197463 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235875115 | GAATAGAGGGAACAG[C/T]GGGTATAAAGACTGG | 1130 |
rs372271452 | snp | A/G | 8.24029e-05 | 0.00641831 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791787 | AGTACTCTCAGCTTC[A/G]TGGATACACTCCACA | 1130 |
rs372298460 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | LYST | GRCh38.p7 | 1:235664077 | GGGAAAAAAATCATC[C/T]AATTATGCAAACTAA | 1130 |
rs372303291 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235837130 | CGAGGACCTAGAGAA[C/T]GAGTGTAAGGGAGCA | 1130 |
rs372307733 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235793769 | CTGAAGAAATAGCAA[C/T]ATAACTAAATGTAAA | 1130 |
rs372309456 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763173 | TCTCAAGGGAGATTG[C/T]TCATCCTTGAGGAAA | 1130 |
rs372313856 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235736521 | GAGGTTGCAAGACAC[A/C]AAGATATGATTATCT | 1130 |
rs372323232 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698609 | GGGCGCGGTGGCTCA[A/C/T]GCCTGTAATCCCAGC | 1130 |
rs372330504 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235668596 | TTTCTCATTCTCATA[C/T]GACTAGCTGATATAA | 1130 |
rs372331418 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680759 | AGCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 1130 |
rs372351602 | snp | A/G | 1.67846e-05 | 0.0028969 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810520 | TTATATCTGCTGAGA[A/G]CGGTAGGTTAAAATC | 1130 |
rs372359060 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235780372 | TCACACCACTGCACC[C/G]AAGCCTGGGTGACAG | 1130 |
rs372363225 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235750718 | CTTCCTTATTTAATA[C/T]CTGAATGCACTGTTT | 1130 |
rs372363820 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235757040 | CAACATATGGAGGGG[G/T]ACTTAAAGCTGGATG | 1130 |
rs372391251 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235869923 | TTTGCACTGACTGGC[C/T]GGCCCCTCTGCTTGA | 1130 |
rs372397853 | snp | A/G | 1.66261e-05 | 0.00288319 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809970 | GTGGGCACTACACTG[A/G]CTGCTAAAGGAGAAT | 1130 |
rs372398185 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235776709 | TTTTTTTTTAAAGTA[G/T]TTTTTGACCCTTAGT | 1130 |
rs372407559 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711767 | GCACATTATAACTTT[G/T]GTATTCAGAAAAAAG | 1130 |
rs372417775 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235826155 | ATATTAGAGAGGATA[C/T]AGAACTGGAATTCTC | 1130 |
rs372435862 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235762021 | GAGATATGCCTAATG[C/T]TAAATGACGAGTTAA | 1130 |
rs372452626 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878595 | TCACAGTAATAGCTG[A/G]CCAGGAAATGTATTG | 1130 |
rs372493317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756664 | GCATTTACTCATTCA[A/G]TAATATACTTAGTAC | 1130 |
rs372498399 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674964 | GTATTCGTGGATCAA[A/G]GCAAAGGCTTATAGA | 1130 |
rs372499435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780007 | CCTACATTATATACT[A/G]GTAGAACAAAATATT | 1130 |
rs372505253 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727685 | AAGCTATGTGAATAT[C/T]AGAATTACTTAAGTT | 1130 |
rs372506770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235753547 | TTATTTTAATTCATC[C/T]ATGAGCCCTTTATGT | 1130 |
rs372508236 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693279 | CAAGATGTGTCACTG[C/T]GCTCCAGCTTGGGCG | 1130 |
rs372515103 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235719737 | CTTTTCCAGTCTCTA[C/G]GAAATACAGGGGTTA | 1130 |
rs372528381 | snp | G/T | 2.01315e-05 | 0.00317259 | intron-variant | LYST | GRCh38.p7 | 1:235793462 | AAATTGTAAGTGAAA[G/T]AATTTATCAGTGAAA | 1130 |
rs372535527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795121 | CAGAGCAGTAAGAAG[C/G]CGAGCTGTCCATCTA | 1130 |
rs372537681 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235752637 | ATTAGGGTTATTTTT[A/C]GGACTAAAAGAGGTA | 1130 |
rs372539657 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829199 | CAGAGCGAGACTCTG[G/T]GTCTCAAAAAAAACC | 1130 |
rs372543784 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235764586 | CTAACTGCAACCACC[A/G]CTTCCCGGGTTCAAG | 1130 |
rs372550583 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845683 | GGCCCTTCTGTTTGC[A/G]TGGGAGCTGGGTGAG | 1130 |
rs372555753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235880853 | TTTAGCGGCCGGGCA[C/T]GGTGGCTCACACCTG | 1130 |
rs372557971 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846508 | TTCACCAGCAATAGA[A/T]CCAAACCAAGAAGAA | 1130 |
rs372571295 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746898 | AATCAAGTTTTAATG[C/T]ACATAATTTTTTAGT | 1130 |
rs372587752 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687322 | TGTGTGTGGATATAT[A/G]TGTATATATATTTAG | 1130 |
rs372625856 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235786764 | CGGACACGGATGAAG[A/C]TGGAAATCATCACTC | 1130 |
rs372628149 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672194 | TTAAGTTGAAAATGC[C/T]GTGTAGGCAATTAGA | 1130 |
rs372645695 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235698812 | TGGGAGGCAGAGCTT[A/G]CAGTAAGCCGAGATC | 1130 |
rs372654270 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770199 | AAAGTGATGAACCAC[C/T]TGAGCTTTCAATAAC | 1130 |
rs372713352 | snp | G/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867043 | GGCTCCGCCTCGCGC[G/T]TGTAAGCCCCGCCTC | 1130 |
rs372726269 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847857 | ACAATCCTAAACATA[C/T]ATGCACTTAACACTG | 1130 |
rs372739017 | snp | C/T | 0.000136398 | 0.00825713 | intron-variant | LYST | GRCh38.p7 | 1:235724217 | AAATATTTGTTTTAC[C/T]GGAAATATAAATAAT | 1130 |
rs372743738 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820743 | ATTTTCCATGCATAA[A/G]CAGGAATATATGTGT | 1130 |
rs372754364 | snp | C/T | 0.00025742 | 0.0113421 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746502 | CAGAAGCGATTCAGT[C/T]TGAGCAAGGGGAAAT | 1130 |
rs372774380 | snp | C/T | 0.000132264 | 0.00813109 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830375 | AAAGCCGGTTGACAT[C/T]GGTCAGAAATTCACG | 1130 |
rs372868836 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | LYST | GRCh38.p7 | 1:235687005 | CGCATTTGCTTCCAG[C/T]AAACAGCTGGCAACT | 1130 |
rs372877124 | snp | A/G | 1.71867e-05 | 0.00293139 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780948 | TTTCTTTATTAATAT[A/G]TTTGGAGTAGTCATT | 1130 |
rs372886987 | snp | A/G | 3.31488e-05 | 0.00407103 | intron-variant | LYST | GRCh38.p7 | 1:235757477 | AAACAGAGACCAAAA[A/G]AGTCTTACTAACATG | 1130 |
rs372892911 | snp | A/G | 0.000376062 | 0.0137073 | intron-variant | LYST | GRCh38.p7 | 1:235804679 | TTCTAAGGTAAAATA[A/G]AAGAGACTAAGAATA | 1130 |
rs372911664 | in-del | -/AAA | | | intron-variant | LYST | GRCh38.p7 | 1:235780418 | CTTAAAAAAAAAAAT[-/AAA]AAATAAAAAAGAGTA | 1130 |
rs372947632 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752036 | TTTGCTATTTTGAAG[A/G]TATCCAAGCATTACA | 1130 |
rs372953700 | snp | A/G | 0.000109757 | 0.0074072 | intron-variant | LYST | GRCh38.p7 | 1:235712221 | AAATACAAATAATAC[A/G]ATTAAGACACAAAGA | 1130 |
rs372953968 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235666877 | GTCACTGGAAACATA[A/G]CCATAAAAGATATTG | 1130 |
rs373013367 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235744334 | AGAAAGTGAATTTAC[A/G]TAAAATAACAGAAAT | 1130 |
rs373031280 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772076 | AAAAAAAATTAAAAA[A/T]TATCCAAGCATGGTG | 1130 |
rs373033967 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235733449 | AAATTCCGTTTAACA[C/T]CAATATCTTAAATCT | 1130 |
rs373039083 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235709784 | TAGTTTAAAAACTCA[A/G]CTAATATAAAGTATA | 1130 |
rs373073426 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235782749 | AAGTCTCCCATCTTG[A/T]CAAACAATTCCAAAA | 1130 |
rs373105684 | in-del | -/GATAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235775989 | TACTAAACATATAAA[-/GATAAA]AATGTAAACATTTTA | 1130 |
rs373107751 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | LYST | GRCh38.p7 | 1:235723998 | ATGAGCACTTAAACA[A/G]TATATATCAATTAAT | 1130 |
rs373110254 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235791237 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCTA | 1130 |
rs373127205 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808823 | AGGACTGGATAAACT[C/T]GAGGAGAGTTCAGCA | 1130 |
rs373132276 | snp | A/C/G | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883531 | ATACAACTTTCCCAC[A/C/G]TAAGAATGAATAAAC | 1130 |
rs373137314 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835896 | TTCATAGCTATAATG[C/T]CCAATTTTAAATCTA | 1130 |
rs373149336 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235744945 | TAAAAAAAGCTAAAA[A/G]AATAATAATAACTTG | 1130 |
rs373193485 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235754229 | TTTTTCTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 1130 |
rs373195142 | snp | C/T | 6.68863e-05 | 0.00578262 | intron-variant | LYST | GRCh38.p7 | 1:235697065 | ATCCAGAATGATCTT[C/T]GTTACATTTTATTTT | 1130 |
rs373212564 | snp | C/G | 4.9552e-05 | 0.0049773 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759081 | GCCAACGGCCAACAG[C/G]TGCAGATCCGTTCTG | 1130 |
rs373213082 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235841238 | AAATAGCAAGTATAG[A/G]CTCTCCTGAGAAGGC | 1130 |
rs373220977 | snp | A/G | 9.88777e-05 | 0.00703058 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759297 | GGACATCACTGACAG[A/G]GACCTGGGCTGAGAG | 1130 |
rs373265404 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235872170 | GCATAGTGGCACATG[C/T]ATGTAGTCTCAGCTA | 1130 |
rs373281155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693832 | AAATAAATATGAACT[A/G]GATACTATTTAACTT | 1130 |
rs373286293 | snp | A/G/T | 3.32813e-05 | 0.00407919 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808694 | ATTTGCAATCTGTAT[A/G/T]CTATGTAATCTGTCT | 1130 |
rs373289598 | snp | A/C | 1.6591e-05 | 0.00288015 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800931 | TTTCAAAAAACTCTC[A/C]AATACATGGGCAAGC | 1130 |
rs373300870 | snp | A/G | 0.000115937 | 0.00761283 | intron-variant | LYST | GRCh38.p7 | 1:235770127 | AAACAACTGTGGAAT[A/G]TATTTCCAAAAGTAA | 1130 |
rs373305377 | snp | A/G | 3.30077e-05 | 0.00406236 | intron-variant | LYST | GRCh38.p7 | 1:235677045 | CTGGCCGAATGCGCT[A/G]TTAGAGCACCAGCCA | 1130 |
rs373356106 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235836716 | TCCCCAAGAATGCAA[A/G]TCCCTCCCAATGCCC | 1130 |
rs373380972 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235789276 | TGATTTAAAAAAAAA[-/T]ATCATATTACAAATT | 1130 |
rs373395043 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235755770 | GAACACAGAAAGCTT[-/A]AAAAAAATGCCACCA | 1130 |
rs373436668 | snp | A/C | 1.66222e-05 | 0.00288285 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800354 | CTGTGTTAAAATACT[A/C]AAGAACCCTCCTAAA | 1130 |
rs373446522 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235815071 | TTCTCTAACACCCTA[C/T]CTGCTTCCCTTAGTA | 1130 |
rs373489106 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711018 | CAACAGCATGAGACA[C/T]CCTGAGCTAAAACCA | 1130 |
rs373497378 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235716046 | CTTGATTTCCACAGC[A/G]ATGACGCATTTTCAA | 1130 |
rs373514480 | snp | C/T | 1.65151e-05 | 0.00287355 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733683 | TTTGAATCCAGACGC[C/T]GAAAGAGACTAAACA | 1130 |
rs373521868 | snp | C/T | 1.65913e-05 | 0.00288017 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781944 | TTGAAGAGAAGCAAA[C/T]TTCCCAGGTCCCATT | 1130 |
rs373529106 | snp | C/T | 6.5925e-05 | 0.00574092 | missense | LYST | GRCh38.p7 | 1:235697179 | AGCCAAATCTTTCTC[C/T]GTGGGGCTGGCTGAA | 1130 |
rs373538023 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810147 | GGAATAATCTCTCTG[A/G]AATTTTCCAAAGCCA | 1130 |
rs373572593 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759099 | CAGATCCGTTCTGTG[A/G]AGGAAAAGCTAGCCC | 1130 |
rs373577384 | snp | C/T | 0.000511496 | 0.0159839 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806382 | TGAGTCATTGGCCGA[C/T]TCCCTGTCAGACTCT | 1130 |
rs373585443 | in-del | -/AAAG | | | intron-variant | LYST | GRCh38.p7 | 1:235857524 | ATCAAAGGAAAGCAC[-/AAAG]AAAGAGAAATGAGGA | 1130 |
rs373606472 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235765769 | CTCTCCACAGTGGTC[A/G]GATGAAACCCTCTGT | 1130 |
rs373612256 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235704533 | TTTTTTTCATATGTT[A/T]GTTGGTCACACGTAT | 1130 |
rs373613884 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700240 | AATTGACAACTGGGA[G/T]CTAATTAAAGAGCTT | 1130 |
rs373640642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688914 | CGCTTGAACCCAGGA[C/G]GGGGAGGTTGCAGTG | 1130 |
rs373670719 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797700 | TACGGGGAACATTCC[A/G]TAATATTGGATTTGT | 1130 |
rs373671757 | snp | C/T | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806306 | GGCTCTCGAGAGATA[C/T]ACATGGCAGCATATG | 1130 |
rs373676969 | snp | A/G | 3.29598e-05 | 0.00405941 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734490 | TGACTCACCTCTTTG[A/G]TCATTTTAATAAGGT | 1130 |
rs373690076 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235688965 | ACTCCAGCCTGGCAA[A/C]AGAGTGAGACTCCGT | 1130 |
rs373694701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701884 | TGACATATGTGAGCT[A/G]TGAGCGCAAATAATT | 1130 |
rs373758465 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235848864 | GACCCAGCGAGATTG[A/C]AATGGTAATTTAATA | 1130 |
rs373776104 | snp | A/G | 3.2963e-05 | 0.00405961 | synonymous-codon | LYST | GRCh38.p7 | 1:235677113 | ACACACAGTAGCAAT[A/G]TCACCTGAGGTTTCA | 1130 |
rs373798957 | snp | C/G | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753112 | ACCATTATCCAGCAA[C/G]ATATCTGCTACCTTA | 1130 |
rs373811121 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662477 | AAATTATCTTTTTTT[C/T]TTTCCTCTTTTGGAG | 1130 |
rs373816415 | snp | A/G | 6.59761e-05 | 0.00574314 | intron-variant | LYST | GRCh38.p7 | 1:235693530 | AGATTGTCACTGCTC[A/G]ACTGTTACATGACAG | 1130 |
rs373836609 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235751655 | AGGCAAAAGTTTAAC[C/T]GGCAATTATCATATT | 1130 |
rs373840046 | snp | C/T | 6.64253e-05 | 0.00576266 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800335 | CTTGAAAATCAGAAT[C/T]ATCCTGTGTTAAAAT | 1130 |
rs373874587 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYST | GRCh38.p7 | 1:235779097 | GTCTCAAACTCCTGA[C/T]CTCAGGTGATCCACC | 1130 |
rs373874724 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235774761 | ATGAAAAGAACTAGA[A/G]GAGTATCTTAGTTTG | 1130 |
rs373880416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679727 | CCAGGGAATTCCAGG[A/G]TTCTCCCATGCAACT | 1130 |
rs373892036 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235835819 | TACTTATCTATGACT[-/G]TTTCACCCTCTAGGT | 1130 |
rs373917160 | snp | C/T | 4.94768e-05 | 0.00497352 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830259 | TAGCTTGGTAAGTAA[C/T]AGAAATCCTCGACCA | 1130 |
rs373928344 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710676 | CACAAGGCAAAGTCT[A/G]TCTTCCTTTCTTTTG | 1130 |
rs373930104 | snp | A/G | 1.66112e-05 | 0.00288189 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788757 | GATCATCAACGCTTT[A/G]GATCCCAGTGAAATT | 1130 |
rs373933831 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809042 | ATGGAGCAAAGGAAT[A/G]ATTACAGATTTGGGA | 1130 |
rs373936244 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687855 | AAGGTCAGCCTTGCC[C/T]CATCCTCAGGCTTCC | 1130 |
rs373945489 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235783888 | ATTCTTTTTTTTTTT[-/CT]TTTAAATTGAGACAG | 1130 |
rs373946090 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235668149 | GTTGGTTGAATCCAC[A/G]GATGTGAAACCCACA | 1130 |
rs373948463 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790456 | GAAAGCACTCAATGC[A/G]CATTAGATAGCATAA | 1130 |
rs373960529 | snp | G/T | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724158 | CAGGAAAATGATGCT[G/T]GTTCCAACTCTCCCT | 1130 |
rs373971587 | snp | C/T | 0.000390774 | 0.0139726 | intron-variant | LYST | GRCh38.p7 | 1:235774902 | TAAGAATAAATTTTA[C/T]GAAGACATACCTTCA | 1130 |
rs373988631 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235830194 | AACTATCATATATTG[A/G]TGAAAGTAAGTATTT | 1130 |
rs374004334 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235690366 | TAATATGTTTTTGTG[C/T]TTTCATTTATTTTGT | 1130 |
rs374004441 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235811134 | CAGGTGACAGAGTGA[C/G]ACTCTGTCTCAAAAC | 1130 |
rs374034216 | snp | C/T | 6.6072e-05 | 0.00574732 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777260 | TCACTGGTTCATAGA[C/T]GGTATACTGAGCAGG | 1130 |
rs374043151 | in-del | -/AAAAGAAAAG | | | intron-variant | LYST | GRCh38.p7 | 1:235755389 | GCGAGACTCCGTCTC[-/AAAAGAAAAG]AAAAGAAAAGAAAAG | 1130 |
rs374084801 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235876835 | CTTTAAGCCTAAGCT[A/G]TGTTTATGACTAGAA | 1130 |
rs374099882 | snp | C/T | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755586 | AGCAAGGAAAATCCA[C/T]GATTCTTCAGAAATT | 1130 |
rs374130514 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682640 | CCATAGAAATGTAGT[C/G]GGATGAAAGAATATA | 1130 |
rs374138099 | snp | A/G | | | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800880 | TTTTACCTGTTGCAT[A/G]AGCAGAAAAACATTC | 1130 |
rs374148707 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235804242 | ATTTCTGTCTTAACT[C/T]GAAGTAATTCTCAGT | 1130 |
rs374151347 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235835051 | GCCTCCCGAGTAGCC[A/G]GGATTACAGGCGCCC | 1130 |
rs374155665 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771896 | TTTATTACTAATAGA[C/T]TAGAAAAGGTTTTTT | 1130 |
rs374166269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745270 | TTGGAGTGTATTTCT[C/T]TGAATAGCTTTTTTT | 1130 |
rs374213434 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235799587 | CCAAAATTAAAGTCT[C/T]GTGTAGGCTAGCCTT | 1130 |
rs374215621 | snp | A/G | 1.65814e-05 | 0.00287931 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788838 | TGCACCTTCTGGTCT[A/G]TCGCTCTCTATAAGA | 1130 |
rs374234827 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | LYST | GRCh38.p7 | 1:235663970 | TGAAGCATAAGAGGG[A/G]GAGAAGATCTTACCT | 1130 |
rs374236487 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235783017 | TTTCTCACAGAAAGA[C/T]ACACAAAGCAGGGAG | 1130 |
rs374236670 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235705482 | ACTTGAACTCCTGGG[C/T]TCAAGTGATCCTACT | 1130 |
rs374237283 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235735421 | AATCTTTTATTAACA[A/G]GCCCTAAAACCAAAA | 1130 |
rs374238501 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235753928 | GGTCTGAATTTGTCT[A/G]TCACAATAAGGAGAC | 1130 |
rs374240863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685448 | TATACCATTTTAATG[A/G]CTCCTTAGACTAAGA | 1130 |
rs374244269 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718481 | CTGAGTAGTTGGTCT[C/T]GAACTCCTGACGTCA | 1130 |
rs374248885 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235702056 | AAGGTCCTTTACAAC[A/G]TCTTTCCCTTACCTT | 1130 |
rs374256027 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235667813 | GACTACAGGCGAGTG[C/T]CACCATGTCTGGCTA | 1130 |
rs374258280 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826329 | GGACTTTTATAGGAA[C/T]GTTCAAAGCAGCTTT | 1130 |
rs374263042 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235692515 | CCTCCTGAGTAGCTG[A/G]AATTACAGGAATGTG | 1130 |
rs374281478 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860471 | TCAGAATAGTTTCAC[C/T]GCCCTAAAAATCTTC | 1130 |
rs374284011 | snp | C/T | 9.90491e-05 | 0.00703667 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809428 | AATGCTCTGAGGCCT[C/T]GGGAGGAACTCCATC | 1130 |
rs374290515 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235694850 | CTTTTTTTTTTTCTT[C/T]CAGAAAAAGAAACTT | 1130 |
rs374328302 | snp | C/G/T | 0.0228947 | 0.104514 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235866879 | CGCCGCGCACTCCCC[C/G/T]TCTCCCGGAGAACCC | 1130 |
rs374351038 | snp | C/G/T | 0.000132483 | 0.00813795 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766121 | TGGGATTGTGACAAA[C/G/T]GTAAGTATTAGTAGG | 1130 |
rs374353330 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740276 | TCTATTGAGGTATAA[C/T]TTACATATAATAAAG | 1130 |
rs374368879 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676987 | ACCAAAGTATTTAGA[C/T]CTGGCAGGGACCTGA | 1130 |
rs374399244 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235863208 | TCATCCAGGCTAACA[C/G]AGTGAAACCCCATCT | 1130 |
rs374401277 | snp | C/T | 0.00051546 | 0.0160457 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808438 | CCGCCCCCGCCGCCA[C/T]CCACACACATACAAA | 1130 |
rs374402769 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | LYST | GRCh38.p7 | 1:235693320 | ACTCCGTCTTAAAAA[C/T]AAATAAATAAAATAA | 1130 |
rs374429343 | snp | C/T | 6.59718e-05 | 0.00574296 | intron-variant | LYST | GRCh38.p7 | 1:235728061 | ATGTAAATACAGACT[C/T]AAGCCTCTACTCACC | 1130 |
rs374441344 | snp | C/T | 1.70796e-05 | 0.00292224 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800904 | AACATTCTTTTCTTT[C/T]TGCCTAATAATTTTC | 1130 |
rs374445954 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832671 | ATTATAGTTTACTAT[G/T]TAGCCAATCTCTTAT | 1130 |
rs374451356 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235664454 | AAAAAGAGAATCCAA[A/G]TTCCTCTTACCTTAC | 1130 |
rs374496900 | snp | A/C | 0.000197785 | 0.0099425 | intron-variant | LYST | GRCh38.p7 | 1:235804481 | CATACCCAAAGAACA[A/C]AACTATATGTTGTTA | 1130 |
rs374508384 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235798885 | TACAGGGTTTCTTTT[C/G]GGGGTGATGAAAATG | 1130 |
rs374526313 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235773679 | AGTTTTGGTTTTACA[A/G]AACAAAAAAGATTTA | 1130 |
rs374531662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235742057 | TGAGATATCTAGAAC[A/G]GTCAAACTCACAGAG | 1130 |
rs374540616 | in-del | -/CCTCCCTCTTCCGTGC | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865328 | CTCCCTCTTCCCTGC[-/CCTCCCTCTTCCGTGC]TTTTTCTCTGTAGTA | 1130 |
rs374559316 | in-del | -/CACAATATCATGCAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235724631 | ACATGTATCCACCAA[-/CACAATATCATGCAAA]ATAGTTTTATTGCCC | 1130 |
rs374564733 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235861947 | TTAGGCTAATCCCTG[A/C]ATATTACTAACTTAC | 1130 |
rs374566922 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864669 | GAGCGCAGTGGCTCA[C/T]GCCTACAATCGCAGA | 1130 |
rs374572975 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884559 | GTTTGAAGCATGGAT[A/G]CTGCCACTAGCTTTC | 1130 |
rs374580835 | snp | A/T | | | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235808206 | CTCAGTAAAAAATGC[A/T]TACATACATAAACAA | 1130 |
rs374668321 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235849921 | GCTCATGGATGGGTA[A/G]AATCAATATTGTGAA | 1130 |
rs374692527 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235698690 | TCCTGGTTAACATGG[C/T]GAAACCCTGTCTCTA | 1130 |
rs374695191 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808420 | AGACATGCTCAACAA[C/T]CCCCGCCCCCGCCGC | 1130 |
rs374695724 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764495 | CTTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 1130 |
rs374696016 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681715 | AGGTTTTAATTGTAG[A/G]AAAATCTCAGTCATC | 1130 |
rs374750931 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819008 | CTCAAGAGAAAGGAA[G/T]AACATTCCTGTTGCC | 1130 |
rs374778426 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235760478 | GCTTCTAATATTCTA[C/T]GCAGGAAGACACCAG | 1130 |
rs374779441 | snp | C/T | 0.00024467 | 0.0110578 | intron-variant | LYST | GRCh38.p7 | 1:235775120 | GGATATAGTTTTCTC[C/T]CAATTTGCTGAGAGT | 1130 |
rs374779988 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814211 | AGGTTGGGATAAAGA[C/T]GATGGATTCACTTTT | 1130 |
rs374781952 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883639 | TCTTAGAAGCCCTTG[C/T]GTTGCTTTTTCGTTT | 1130 |
rs374793881 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235732185 | CATCATTTTGAATGG[C/G]TGCCCAATAAAGAGG | 1130 |
rs374796704 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235695478 | AATTTGAGCGAACAT[A/G]GCTATTAAGGGCACA | 1130 |
rs374799594 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858437 | ATCTTGGCTATCCAC[C/T]CATCATTGGTCATTC | 1130 |
rs374814184 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727815 | GTAATAAGAAGGAAT[G/T]AACATAAATTGATAT | 1130 |
rs374830793 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235812505 | AGTGAGACTCTGCCT[-/AA]AAAAAAAAAAAAAAA | 1130 |
rs374841157 | snp | A/C | 6.85565e-05 | 0.00585436 | intron-variant | LYST | GRCh38.p7 | 1:235810571 | GCTTAGAATACCTCA[A/C]TATGTTTTAAAACTC | 1130 |
rs374844894 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235869391 | GCAGGAGAATAGCGT[A/G]AACCCGGGAGGCGGA | 1130 |
rs374859516 | snp | C/G | 0.000156585 | 0.00884692 | intron-variant | LYST | GRCh38.p7 | 1:235830459 | AAAAAAAAAGATTAG[C/G]AAAACAAATACAAAT | 1130 |
rs374933446 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235876585 | TTATTATTATACTTG[A/G]GGAGATTTTATTTAA | 1130 |
rs374949148 | snp | A/G | 0.000249786 | 0.0111728 | intron-variant | LYST | GRCh38.p7 | 1:235802896 | ATTACAAGCACTTCA[A/G]TGATATTTTACCATC | 1130 |
rs374950366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665341 | TTGGCCAGGCGTGGT[A/G]CCTCATGCCTGTAAT | 1130 |
rs374951289 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235801424 | TTCTGACCCCCCCCT[-/A]CAAATACCTAAATCA | 1130 |
rs374961974 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680519 | GTCCCACCTGGGAAG[G/T]CCTCCCAAAGTGCTG | 1130 |
rs374980644 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235883082 | TCATCCACCAGTCAC[C/T]TTTCTCGGTGGTACT | 1130 |
rs374986787 | in-del | -/T | 0.414905 | 0.187899 | intron-variant | LYST | GRCh38.p7 | 1:235694011 | CTTCTCTTCTTCTTC[-/T]TTTTTTTTTTTTTTT | 1130 |
rs374986979 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235816536 | CCAAACTACCAATGA[A/C]ATTCTTCAAAGAATT | 1130 |
rs374995715 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235849749 | GAGAATCAAATAAAA[A/G]AACTCAACCCCTTTT | 1130 |
rs374999975 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235785011 | TTCTTGCTTGTGGCA[A/G]ACACCATGGACTGTA | 1130 |
rs375015154 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235723647 | CCTGACGAGAGTGGT[A/G]AGAAGTCTGTCTGAA | 1130 |
rs375026517 | snp | A/G | 3.79219e-05 | 0.00435425 | intron-variant | LYST | GRCh38.p7 | 1:235805692 | TATATGTGTGTGTGT[A/G]TATATATGTATATAT | 1130 |
rs375038258 | snp | A/G | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730924 | TTCAAACAGGTAAGA[A/G]AGTGGTGGTTTGACA | 1130 |
rs375053252 | snp | C/T | 0.000279057 | 0.0118089 | missense | LYST | GRCh38.p7 | 1:235712086 | AGGAACTCTGGAAGA[C/T]AGAAAAACTCTGGGA | 1130 |
rs375070177 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | LYST | GRCh38.p7 | 1:235769768 | ATTCTAGCATATAAA[A/G]TAGACCGTTAGCAAG | 1130 |
rs375082593 | snp | A/G | 3.2981e-05 | 0.00406071 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746407 | AGTTCCGTTTCAGTT[A/G]CTTGGCTAGGGTTCT | 1130 |
rs375088963 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235767973 | CCTCTTAGCTTTTCA[A/G]TTACTCTTTCTGTAT | 1130 |
rs375106444 | snp | A/G | 4.94531e-05 | 0.00497234 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830308 | AGGGTTGCCATGTGC[A/G]TCTCCTCCTCTTCTT | 1130 |
rs375114936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235839419 | CCTCCACCCTTCCAA[A/G]GTGCTGGGATTACAG | 1130 |
rs375114961 | snp | C/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738137 | GAAGGACTTGGCAGG[C/G]GAACTTGCTCTTGTT | 1130 |
rs375118833 | snp | A/C/T | 3.45681e-05 | 0.00415729 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808417 | TCTAGACATGCTCAA[A/C/T]AACCCCCGCCCCCGC | 1130 |
rs375127531 | snp | A/G | 3.30415e-05 | 0.00406444 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792041 | TTAAATTTGGAGCGT[A/G]CAGTAAAGGGAAGGT | 1130 |
rs375131553 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671360 | AATGCATTGAATTTT[A/G]TCAAATGCTTTTTTC | 1130 |
rs375135845 | snp | A/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777287 | CAGGACAGTAAGTTG[A/T]ATAAACAACTGAAAG | 1130 |
rs375140620 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693038 | AAAAAAAAGTTGGCC[A/G]GGTGTGGTGGCTCAC | 1130 |
rs375145903 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235700658 | AAGCAGTATGGTGTC[A/G]AAAGTTTCACCGTGG | 1130 |
rs375154284 | snp | A/G | 0.000153988 | 0.00877328 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766142 | TATTAGTAGGAGGGT[A/G]AACTGCTAAAAGGAA | 1130 |
rs375172028 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235731013 | ATATTTATATGTTGA[C/G]TCAAGAAGCCACTAT | 1130 |
rs375174233 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687697 | CGCAGCAACTGTCCC[C/T]AACTGCTCTCCTGTC | 1130 |
rs375187995 | snp | C/G | 8.34996e-05 | 0.00646087 | intron-variant | LYST | GRCh38.p7 | 1:235715369 | AGTACTGAAAGAAAC[C/G]GTGAATCCAGAGAAT | 1130 |
rs375190884 | snp | C/T | 0.000132759 | 0.00814628 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808442 | CCCCGCCGCCACCCA[C/T]ACACATACAAACCTG | 1130 |
rs375235690 | snp | G/T | 3.30874e-05 | 0.00406726 | intron-variant | LYST | GRCh38.p7 | 1:235751386 | AGAAGATACTAGAAT[G/T]TTTTCAAGCTATGTG | 1130 |
rs375237666 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806354 | CTGTGCTGTCATAGC[C/T]AGAAGTATCTTCTGA | 1130 |
rs375248990 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235795676 | TTCCACATACTACCC[A/C]CTCAGGAAAGAGGCC | 1130 |
rs375269382 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680419 | ACTACCATGCCCAAC[C/T]ACTTTTTAAATTTTT | 1130 |
rs375294916 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859401 | CCTCAAGCTTCTACC[C/T]ACTAACCTCCCTTCA | 1130 |
rs375297185 | snp | A/C | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235758997 | TTGCAGTTCGGTTGT[A/C]ATTTGGCTCATAACC | 1130 |
rs375311325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685825 | CACTCTGGCCTGGGC[A/G]ACAGAGTGAGACTCT | 1130 |
rs375312576 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235677036 | GAGTAACCACTGGCC[A/G]AATGCGCTGTTAGAG | 1130 |
rs375315039 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810523 | TATCTGCTGAGAGCG[C/G]TAGGTTAAAATCTAA | 1130 |
rs375324243 | snp | C/G | 3.30278e-05 | 0.0040636 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759089 | CCAACAGCTGCAGAT[C/G]CGTTCTGTGAAGGAA | 1130 |
rs375329356 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695595 | ACCTGCTCTTTCTCT[C/T]TTGCTCAACAGAGAG | 1130 |
rs375332299 | snp | C/G/T | 6.64037e-05 | 0.00576178 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809892 | CCTGCAGAAACTACT[C/G/T]GACTCTCCAAGTTGT | 1130 |
rs375375564 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813300 | AGCACACTCCTGCTG[A/G]TATTTCCAAAAATAG | 1130 |
rs375382586 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235864399 | AGTAAACAAGTACCC[C/T]ATCTTTCTACTTGTT | 1130 |
rs375416857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754516 | AGGCTTGAGCCACCA[C/T]GCCCAGCCTCACCTG | 1130 |
rs375422713 | snp | C/G/T | 0.000759941 | 0.0194785 | intron-variant | LYST | GRCh38.p7 | 1:235770150 | AAAAGTAAAGTTACA[C/G/T]GAAAAGTACCTGCAA | 1130 |
rs375448708 | snp | A/C/G | 8.32361e-05 | 0.00645073 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808745 | ATAAGCCTTTAAAGC[A/C/G]TCCCATTTCCACAAC | 1130 |
rs375451892 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235879204 | ACAACTATGAGGTGA[A/G]TATCCTACCCACTTG | 1130 |
rs375460313 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853680 | TTAACATGCCATTCC[A/G]GCTGCCTTGAAACCT | 1130 |
rs375463934 | snp | A/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235663909 | TTTCTTTAAGTCTGT[A/G/T]TGCTTAAATACCTCT | 1130 |
rs375484347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751656 | GGCAAAAGTTTAACC[A/G]GCAATTATCATATTT | 1130 |
rs375487357 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763316 | ACAAATGCAACAAAT[C/T]TAAATCCGAATCATC | 1130 |
rs375489568 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235737162 | ACCATAATAGTATGC[C/T]AAGAAAAAAAGAACC | 1130 |
rs375589572 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235837682 | GATGAAGACTGGGAA[C/T]TGACTGCTGGATTTA | 1130 |
rs375597373 | snp | G/T | 1.64825e-05 | 0.00287071 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702927 | CATGGTTTCTAGCGC[G/T]CGTCTCTGAACTGGA | 1130 |
rs375624853 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235754250 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTCACT | 1130 |
rs375640588 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235691917 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 1130 |
rs375646298 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672259 | CTGGAAAAATAAATT[C/T]AGGAGTCATTAGGGA | 1130 |
rs375654642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235826254 | ATTAAACAAACATTA[A/C]CCTTTGCCCACAAAT | 1130 |
rs375665715 | snp | A/G/T | 0.000263778 | 0.0114815 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759180 | GGTAATCAGGTCGGC[A/G/T]TGGGCAGGACTCATC | 1130 |
rs375670550 | snp | A/G | 1.65053e-05 | 0.0028727 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806433 | AAAAGCCACACAGAG[A/G]AATAGGTTTATTGTG | 1130 |
rs375675197 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741440 | TAGGGATGGGCTGAG[A/G]CAGTCTCGTAGTATT | 1130 |
rs375715423 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235785685 | TGTTAAGTAGTCTCA[A/C]CATGTCCATTCATTT | 1130 |
rs375751973 | snp | C/T | 4.94238e-05 | 0.00497086 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755515 | GACCAAAGAACATTT[C/T]GATGAAGCATTCTAA | 1130 |
rs375756077 | snp | C/G | 1.68369e-05 | 0.0029014 | intron-variant | LYST | GRCh38.p7 | 1:235802865 | TTGCTATTTAATGAT[C/G]TGGCTTGCAGATCTA | 1130 |
rs375783616 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731097 | TAACATCTCTGTAAA[A/C]GTCTCCTCTCTCGAT | 1130 |
rs375785129 | in-del | -/CAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235769031 | TAAAACAAAACAAAA[-/CAAAA]ACCATATCCCTGCTT | 1130 |
rs375792494 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693293 | GCGCTCCAGCTTGGG[C/T]GGCAGAGTGAGACTC | 1130 |
rs375802525 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235835102 | TTGTATTTTTAATGG[-/TG]GGGGGGGTTTCGCCA | 1130 |
rs375839384 | snp | A/G/T | 3.29637e-05 | 0.00405968 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731161 | TTGGATAGTAGATGG[A/G/T]GTCATACCATACTGC | 1130 |
rs375846718 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752462 | GTTGTAAGTGTAACA[C/T]TAGAGATTAATACAC | 1130 |
rs375855944 | snp | C/T | 3.62312e-05 | 0.00425609 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830421 | GTCGGTGCTCATGAC[C/T]GAGCTATAAAATAAG | 1130 |
rs375877609 | snp | A/G | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235866970 | CAGGAAACCGAGAAC[A/G]CCACCCCCTCCCTCC | 1130 |
rs375881446 | snp | A/G | 9.36847e-05 | 0.00684351 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746516 | TTTGAGCAAGGGGAA[A/G]TTTTCGAGGACCTTT | 1130 |
rs375913035 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235871260 | TCTCTACTAAATCAC[-/C]AATAGCATTTGAAAT | 1130 |
rs375913409 | snp | C/G/T | 0.000187681 | 0.00968543 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774936 | TGTAAAACCCAACAA[C/G/T]GCATTTTTGTTTGAT | 1130 |
rs375940652 | in-del | -/AATAATAATAAT | | | intron-variant | LYST | GRCh38.p7 | 1:235688985 | TGAGACTCCGTCTCA[-/AATAATAATAAT]AATAATAATAATAAT | 1130 |
rs375956548 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235782772 | TTCCAAAAACTGGAA[G/T]CCATGACATTCCAAA | 1130 |
rs375966100 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752775 | TACAATGCTTCTCTC[C/T]ATCTGGGTTTTCCAA | 1130 |
rs375979256 | in-del | -/GAGA | | | intron-variant | LYST | GRCh38.p7 | 1:235736433 | TATAGATAGACAAAG[-/GAGA]GAGAGGTGTTCTGTG | 1130 |
rs375982108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870999 | AGAATTATACAGATG[A/G]ATAAAATTATGCATT | 1130 |
rs375984965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699431 | CTCATTATTTTTTAC[A/G]GCTGCATAGTATTTC | 1130 |
rs375993086 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235776190 | CTATTTAACTAGACA[C/G]TAGATTAAAAAAACT | 1130 |
rs375998298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747284 | CATAGGAACCAAAAT[C/G]ATGTCTTGGTAGATG | 1130 |
rs375998552 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820790 | CTTTATTTCTTCTAT[C/T]AGAATTTTATAATTA | 1130 |
rs376007590 | snp | A/C | 8.25702e-05 | 0.00642482 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757442 | AGCATATAGGTACCA[A/C]ACAGTCTTCAGTTAC | 1130 |
rs376008936 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235701410 | CGAGGCGGGCAGATC[A/C]TGAGGCCAGGAGTTC | 1130 |
rs376036029 | snp | A/G | 1.66488e-05 | 0.00288515 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788730 | GGCATTGTGGGGATC[A/G]GCCCACACTTGGATC | 1130 |
rs376038014 | snp | A/C/T | 6.62531e-05 | 0.00575526 | synonymous-codon, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766104 | AGAAAAGTAGAAGTT[A/C/T]GTGGGATTGTGACAA | 1130 |
rs376080581 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235862593 | TTGAGGTCAGCAGTT[-/C]GAGACCAGCCTGGGC | 1130 |
rs376119741 | in-del | -/GT | 0.128632 | 0.218563 | intron-variant | LYST | GRCh38.p7 | 1:235835101 | TTTGTATTTTTAATG[-/GT]GGGGGGGGTTTCGCC | 1130 |
rs376127880 | snp | A/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865437 | TAAGCTCCATGAAGG[A/T]GCAGATATTTATGTT | 1130 |
rs376134468 | snp | C/T | 4.94629e-05 | 0.00497283 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805999 | TCTGATGGTATGGGG[C/T]CACTTTTTATAGCCA | 1130 |
rs376152285 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842715 | GGTTCCCTGGATTAT[C/T]TCCTTTACCTTCTGG | 1130 |
rs376161116 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | LYST | GRCh38.p7 | 1:235693475 | TGTCCGTACTGTTCA[C/T]GCTTCTCACACCTCA | 1130 |
rs376213710 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667853 | ATTTTTAGTAGAGAT[C/G]GGGTTTCACTGTGTT | 1130 |
rs376237991 | snp | A/C | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884287 | CCACTACGCCCGGCT[A/C]ATTTTTTTGTATTTT | 1130 |
rs376238866 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235860576 | GAATGCCATACACTT[A/G]TAATCATAAAGTATG | 1130 |
rs376246381 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235802894 | TAATTACAAGCACTT[C/T]AATGATATTTTACCA | 1130 |
rs376253923 | in-del | -/TATC | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235677410 | GACATTATTTTGGTT[-/TATC]TATTTCATATAGTAA | 1130 |
rs376259384 | snp | A/G | 6.64099e-05 | 0.00576199 | LYST | 1 | allele_origin=G(germline)/A(germline) | 1:235808970 | ATCCAAAATAAGTTT[A/G]TTAAGGATATTCAAT | 1130 |
rs376276274 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724091 | GATTTCTACAGCATT[A/C]TCTCTCAATTGCCAC | 1130 |
rs376280600 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235709833 | TGCCATAGTCTATTA[A/G]TTTTATAAGTCTATG | 1130 |
rs376300162 | snp | C/T | 0.000153988 | 0.00877328 | missense | LYST | GRCh38.p7 | 1:235709260 | GCCCAAGGGGGAAGG[C/T]TGACGTGATTAACCC | 1130 |
rs376311093 | snp | C/T | 0.000282568 | 0.0118829 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762824 | AGGTACATGATTGAC[C/T]GCACTTTCTCCTGAA | 1130 |
rs376338659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235776905 | CTTAATCATCTATGG[A/C]AGAAAGCTTAATAAC | 1130 |
rs376363665 | in-del | -/GAA | | | intron-variant | LYST | GRCh38.p7 | 1:235669006 | TTCTCCTGAACACAA[-/GAA]TAGATGAATGTTTTG | 1130 |
rs376383576 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235725699 | GGAACTAATGGGGCA[C/T]TCCTGCAAATAAAGC | 1130 |
rs376443524 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | LYST | GRCh38.p7 | 1:235677054 | TGCGCTGTTAGAGCA[C/T]CAGCCAGCCCTGTGC | 1130 |
rs376444707 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682330 | ACCCTGTATGCCCAA[A/G]AAGAAAGTGGAGAAA | 1130 |
rs376453140 | in-del | -/A/AAA | 0.5 | 0 | intron-variant, cds-indel, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739623 | GAAAAAAAAAAATAG[-/A/AAA]AAAAAAAAAACGTAG | 1130 |
rs376474918 | snp | A/G | 4.94214e-05 | 0.00497074 | missense | LYST | GRCh38.p7 | 1:235687026 | GCTGGCAACTGTCAG[A/G]CACCCAAGCACAACT | 1130 |
rs376475257 | snp | A/G | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800973 | GGCTTTACTAGCAGA[A/G]AGCAAATTTAATTCC | 1130 |
rs376496670 | snp | C/T | 3.3006e-05 | 0.00406226 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805886 | TTGCTTCCTCGGGAG[C/T]GGCTTCAGTAGCTGA | 1130 |
rs376515575 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861988 | TGAAATTTATAGGAG[G/T]TCACTGGTTTAGACT | 1130 |
rs376528653 | in-del | -/GTT | 0.11546 | 0.210711 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715153 | GTTGTTGTTGTTGTT[-/GTT]TCTGATGACCCAACA | 1130 |
rs376530954 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235782953 | TGCTTCATGGATAAC[A/G]GTGAAGGAATGCTTA | 1130 |
rs376533043 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235691114 | TAGTAGAGACGGGGT[C/T]TCACTGTGTTAGCCA | 1130 |
rs376535164 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235754169 | TAAGGCGTTCCTATA[C/T]GGATCCTTTATGTAA | 1130 |
rs376539648 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717244 | CCTAGTTAGTTAAAA[C/T]TGAAGAAACAACACG | 1130 |
rs376549119 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235758345 | ACGCCTAGGCAATGT[C/G]TGTCATAACATGGAG | 1130 |
rs376594159 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235736022 | GTATTCAATGACATT[C/T]AAAAATTATCTTGAA | 1130 |
rs376605572 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235810622 | CTTATTTATCTTAAA[C/T]CCACTAAAGGAGTTT | 1130 |
rs376607493 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235775157 | TTAACATGTATAATC[C/T]TCCATTCTGTAACAT | 1130 |
rs376645618 | snp | A/G | 6.95398e-05 | 0.00589619 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780922 | TTCTCTGATTTGTTC[A/G]CATCGCAAAATTTCT | 1130 |
rs376674011 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689032 | TAATAATAATAACAA[C/T]AACAACAACAACAAC | 1130 |
rs376718077 | snp | C/T | 0.000222553 | 0.0105464 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800879 | TTTTTACCTGTTGCA[C/T]GAGCAGAAAAACATT | 1130 |
rs376729830 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235749894 | CATTGACCAAATGGG[A/C]AATAGCAAGAGGACT | 1130 |
rs376744187 | snp | C/T | 1.68241e-05 | 0.00290031 | intron-variant | LYST | GRCh38.p7 | 1:235664652 | CATCCGGCGGGTTAC[C/T]AGAATGTGGCTGTCT | 1130 |
rs376751382 | snp | C/T | 1.65296e-05 | 0.00287481 | intron-variant, missense | LYST | GRCh38.p7 | 1:235751377 | TCTAAAAACAGAAGA[C/T]ACTAGAATGTTTTCA | 1130 |
rs376753657 | snp | C/T | 4.94368e-05 | 0.00497152 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791796 | AGCTTCATGGATACA[C/T]TCCACATTAAACCAC | 1130 |
rs376757986 | snp | C/T | 3.35666e-05 | 0.00409661 | intron-variant | LYST | GRCh38.p7 | 1:235800288 | CACATAAAATAATTT[C/T]AGAGCTATTGTTTAA | 1130 |
rs376759438 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840514 | TATCAGAATCACCTA[C/T]AGAGTTTGTCTAGGC | 1130 |
rs376805724 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718533 | TCCCAAAGTGCTGGG[A/G]TTACAGACTTGAGCC | 1130 |
rs376807057 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235765877 | TATTTGAGTCTATGT[A/C]TCCTTTCTCCACTTG | 1130 |
rs376816237 | snp | A/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672058 | AGAAAGAAGGAGAAG[A/G/T]GTAAAGGATGACTCA | 1130 |
rs376817988 | snp | A/G/T | 9.8861e-05 | 0.00703012 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734504 | GATCATTTTAATAAG[A/G/T]TCTGCTTTTGTTGAT | 1130 |
rs376821187 | snp | A/G | 0.000100934 | 0.00710328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813010 | GTATCTTCCATACCA[A/G]TGGAAGGAGAGACAG | 1130 |
rs376860269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686915 | CCCTCATTGACAAAG[A/T]CCCATACTACCCACA | 1130 |
rs376863649 | snp | A/G/T | 0.000222676 | 0.0105495 | intron-variant | LYST | GRCh38.p7 | 1:235830183 | TAGCTACAGTTAACT[A/G/T]TCATATATTGATGAA | 1130 |
rs376872960 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235869480 | CCGTCTCAAAAAAAA[A/T]AATAATAATTAAAAA | 1130 |
rs376882622 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845682 | TGGCCCTTCTGTTTG[C/T]GTGGGAGCTGGGTGA | 1130 |
rs376894393 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817633 | AAACCAAATACTGCA[C/T]GTTCTCACTTTATAA | 1130 |
rs376938449 | snp | C/G | 4.96718e-05 | 0.00498331 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788800 | CCTTCTTCTATGAGT[C/G]TTTCACCAGGATTTA | 1130 |
rs376992402 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813245 | TAAGTTTATAAGCCT[C/T]TCTAATGATAGAAGA | 1130 |
rs376996998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751766 | ACTTGGTAAGAAAAA[C/T]CAGTGACATCTTTCA | 1130 |
rs377030326 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661910 | ATTTTATTATTCTTC[C/T]TAGAATTCTCAGATG | 1130 |
rs377041685 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235776453 | GGAAGATCAAAGCTG[C/T]TTTAATTAAACAGGG | 1130 |
rs377065004 | snp | C/T | 1.82002e-05 | 0.00301658 | intron-variant | LYST | GRCh38.p7 | 1:235773791 | TGGTAAATTTTGTGT[C/T]ATATGCATTTTACCA | 1130 |
rs377126226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839714 | AGGAGGCTAAGGCAG[A/G]AGAATTGCTTGAACC | 1130 |
rs377135630 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235811473 | ATTATTTCTCAAATG[C/T]TTCAGCACTGAACTA | 1130 |
rs377138481 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751003 | AATATTTAGCACAAT[A/G]CTCAGCACATGGTAG | 1130 |
rs377184829 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702796 | TCCCTGAAAGCAAAC[C/T]GCACTAGCAACCCCA | 1130 |
rs377189556 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235710863 | GACATCCAGGGCTGC[C/T]GTGCTGTGGGGAAGC | 1130 |
rs377194100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787555 | CTTAGTTATTCTATC[A/G]TTACCTCAATTCATG | 1130 |
rs377203004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729763 | CAAAGCAGACTAGAT[A/G]GAGTTCCAATAGCAT | 1130 |
rs377213567 | snp | A/G/T | 0.000115525 | 0.00759943 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806694 | TGCTTTTAGAGAATG[A/G/T]CTTCGAATACCATTT | 1130 |
rs377219517 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844418 | GAGAAAAACTGAGGC[C/T]TACAGGTCCAAGGTC | 1130 |
rs377239954 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715929 | CATCATAAAGTAGGA[A/T]GTTCAACCAAACATT | 1130 |
rs377245179 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235693133 | ATCCTTGCTAACACG[A/G]TGAAATCCCGTCTCT | 1130 |
rs377275771 | snp | C/G | 3.33211e-05 | 0.0040816 | intron-variant | LYST | GRCh38.p7 | 1:235724197 | TAAGACAAAGAAATA[C/G]GCAAAAATATTTGTT | 1130 |
rs377294011 | snp | A/C | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235855059 | AAGGGTATACACTTT[A/C]TCAACTAATTTTTTA | 1130 |
rs377299437 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235857653 | AAAACCAAAAAAGAG[C/G]GGGGTGTGTCTGTGG | 1130 |
rs377306581 | snp | C/T | 1.65809e-05 | 0.00287926 | missense | LYST | GRCh38.p7 | 1:235664538 | GGTTGGAGAAAGCCA[C/T]GGAACAGATGATCTC | 1130 |
rs377333889 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752078 | AATAACCCTAAAATA[C/T]TGTGAGCCTGAGGAA | 1130 |
rs377340071 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235872534 | AGCATTCCTTCTTCC[C/T]GGATACAGGGCAGGA | 1130 |
rs377343766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738988 | AAGAGCTGCAATTTT[A/G]AAGTCTTCTGATGTC | 1130 |
rs377386258 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235797562 | TGAGAAAATTGGATA[C/T]TCACACGCAAAATAA | 1130 |
rs377388449 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235691208 | CAGGCTTGAGCCACC[A/G]CGCCTGGCTACAGTT | 1130 |
rs377396577 | snp | C/G | 8.23866e-05 | 0.00641767 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787269 | GGCTGCTGTAAGTAG[C/G]TGAGTACTAAATGTT | 1130 |
rs377401875 | in-del | -/TTTAA | | | intron-variant | LYST | GRCh38.p7 | 1:235811362 | ATAGACCTGATATAA[-/TTTAA]CTACTTTAAGATTTT | 1130 |
rs377431098 | snp | G/T | 0.000153096 | 0.00874784 | intron-variant | LYST | GRCh38.p7 | 1:235743949 | TTCCTTTGTGTGAAT[G/T]AACATTTCCCATGTA | 1130 |
rs377491150 | snp | C/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759054 | CATCAGTGTTTCTAT[C/G]AACAAGACTTGGCCA | 1130 |
rs377498218 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235768318 | AATTCTATCCTTATA[A/C]TCTCTCCCATATTTG | 1130 |
rs377506464 | in-del | -/ACACAC | | | intron-variant | LYST | GRCh38.p7 | 1:235857743 | CAAACATATGTAAAT[-/ACACAC]ACACACACACACACA | 1130 |
rs377526144 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235683397 | ACACGTTACTTACTT[C/T]GTGACAGAATAACCC | 1130 |
rs377528525 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235716397 | TAAATAACACTAGGG[A/G]ATACGAATAGCAGGT | 1130 |
rs377535983 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809222 | TGCAGTCTCTTCAAA[C/T]GGGTTTTTGGAAACC | 1130 |
rs377552790 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235870307 | GGTGTAAACAGGCCA[C/T]AGCCCACACCTGTGT | 1130 |
rs377561348 | snp | C/T | 6.6084e-05 | 0.00574784 | intron-variant | LYST | GRCh38.p7 | 1:235733735 | TAAGCATACATGGAA[C/T]GTATTTATCAGAACA | 1130 |
rs377563551 | snp | G/T | 1.65759e-05 | 0.00287883 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781952 | AAGCAAATTTCCCAG[G/T]TCCCATTTTCCAGCC | 1130 |
rs377579412 | snp | A/C | 1.67063e-05 | 0.00289014 | intron-variant | LYST | GRCh38.p7 | 1:235664451 | CAAAAAAAGAGAATC[A/C]AAATTCCTCTTACCT | 1130 |
rs377581916 | snp | C/T | 9.88826e-05 | 0.00703076 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810198 | TCTTTGGTTGCTAAG[C/T]GGTCAAGTTTAGCTT | 1130 |
rs377597379 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235875865 | AAAAACAAACAAACT[G/T]CATTGAATGTACTAA | 1130 |
rs377600053 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235762227 | TGTGATTGAAAAACA[A/G]ATCATATGGATAGAA | 1130 |
rs377628490 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235736260 | CTGTTAAACATGAAT[A/C]CTTAGAAAATAATAA | 1130 |
rs377638927 | snp | A/C | 6.60219e-05 | 0.00574513 | intron-variant | LYST | GRCh38.p7 | 1:235728032 | TGATACATTTTTGGA[A/C]TCTGTCTAGATTTAT | 1130 |
rs377640576 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | LYST | GRCh38.p7 | 1:235774904 | AGAATAAATTTTATG[A/G]AGACATACCTTCAAA | 1130 |
rs377674323 | snp | A/C | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739443 | CCAGTATATAAATCC[A/C]ATATTGCATGTATGG | 1130 |
rs377677045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682654 | TCGGATGAAAGAATA[C/T]AGAGAAAAATAAAGA | 1130 |
rs377718378 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235883034 | AGCAGTCTGCAGGGG[C/T]CAGCTCCTGGAGGCA | 1130 |
rs377720459 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835473 | GTCTGTTTCTCTTAT[C/T]GAGGGACATTTTCTA | 1130 |
rs377722496 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235805055 | ATGGAGGCTGGAACT[G/T]AAGTAGGAAGAGCCT | 1130 |
rs377723644 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235730659 | ATGACTGAAATCCCA[A/T]GAACTCTTGCTGTCA | 1130 |
rs377725403 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771961 | GGCATGGGGGGCTCA[C/T]GCCTGTATCCCAGCA | 1130 |
rs377732986 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235798532 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 1130 |
rs377737048 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235767020 | ACATAAAATATGTAG[C/G]TAGTACAATTATAAC | 1130 |
rs377766464 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235728243 | TGAATCTCACTACCT[C/T]GACACAGTTCCTGGC | 1130 |
rs386370050 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859509 | ACCAGGCCTTTTTTT[-/T]TTTTTTAAATGTATC | 1130 |
rs386370051 | in-del | -/TTTT | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884122 | CCATGCCCAGCTAAT[-/TTTT]TTTTTTTTTTTTTTT | 1130 |
rs386640621 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | LYST | GRCh38.p7 | 1:235691987 | ACAGGCGTGAGCCAC[CAT/TAC]GCCCAGCCTAACATC | 1130 |
rs386640622 | multinucleotide-polymorphism | CAG/GAA | | | intron-variant | LYST | GRCh38.p7 | 1:235698009 | CACTTCAAGCAAAAA[CAG/GAA]TTATTAAAAAGTTTC | 1130 |
rs386640623 | in-del | ACA/CC | | | intron-variant | LYST | GRCh38.p7 | 1:235702051 | TCTTTAAGGTCCTTT[ACA/CC]ACGTCTTTCCCTTAC | 1130 |
rs386640624 | multinucleotide-polymorphism | CG/GA | | | intron-variant | LYST | GRCh38.p7 | 1:235735365 | CGCAAACCCCACGCA[CG/GA]CAATTCTATGTATGT | 1130 |
rs386640625 | in-del | A/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235761978 | GGGCCTGTTGTCGGG[A/TG]GGGGGAGGGGGGAGG | 1130 |
rs386640626 | multinucleotide-polymorphism | AAC/CAT | | | intron-variant | LYST | GRCh38.p7 | 1:235799039 | GTCATTAAATAATGG[AAC/CAT]ATAATTTCTCAGAGT | 1130 |
rs386640627 | multinucleotide-polymorphism | GC/TT | | | intron-variant | LYST | GRCh38.p7 | 1:235799486 | TCCTTTTGATATGAT[GC/TT]ACTCAAAAGGACCCA | 1130 |
rs386640629 | multinucleotide-polymorphism | CGGGGGCTCGCATTGTGAATTTT/TGGTGGCTTGCATTGTGAATTTG | | | intron-variant | LYST | GRCh38.p7 | 1:235845027 | GGACAGAGCAGCATG[lengthTooLong]AGCTCCAGATCCACT | 1130 |
rs386640630 | multinucleotide-polymorphism | CA/GG | | | intron-variant | LYST | GRCh38.p7 | 1:235860310 | CAGCCCCCCTAAACT[CA/GG]TACATTTGTTATAAT | 1130 |
rs386640631 | multinucleotide-polymorphism | CT/GC | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866174 | TCCCAGCTTATTTAA[CT/GC]CATCAGAAGCGAAGG | 1130 |
rs386640632 | in-del | ATC/TCCTGTGTTGATTTATTA | | | intron-variant | LYST | GRCh38.p7 | 1:235880415 | ATTCTAAGTCAAGGA[ATC/TCCTGTGTTGATTTATTA]CTCGGTAAAAGTGTC | 1130 |
rs397713415 | in-del | -/A/AG | 0.0240643 | 0.107019 | intron-variant | LYST | GRCh38.p7 | 1:235715880 | GATAAAAAAAAAAAA[-/A/AG]GAATATGGTGATTTT | 1130 |
rs397721096 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235877875 | AAAAAAAAAAAAAAA[-/A]TCTAAAACACACATT | 1130 |
rs397744311 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235736856 | CAACAGAAAAAAAAA[-/A]GTCAGTTACCTACAC | 1130 |
rs397756564 | in-del | -/A | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235719641 | TAAAAAAAAAAAAAA[-/A]GGAAAATATATATAA | 1130 |
rs397759940 | in-del | -/C | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235693240 | AGAATGGCGTGAGCC[-/C]GGGAGGTGGAGCTTG | 1130 |
rs397824047 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717718 | CATCTTTTTTTTTTT[-/T]AATATAAATTACTAT | 1130 |
rs397833528 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235730609 | TTGTTAGTTtacata[C/T]acacacacacacaca | 1130 |
rs397840613 | in-del | -/GTT | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715155 | gttgttgttgttgtt[-/GTT]tCTGATGACCCAACA | 1130 |
rs397841091 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235749013 | ATTTAGGAATCCCCC[-/C]TACCACACCTAAACA | 1130 |
rs397844542 | in-del | -/A | 0.40853 | 0.193309 | intron-variant | LYST | GRCh38.p7 | 1:235744893 | GTGAGAACCCATCTC[-/A]AAAAAAAAAAGAAAA | 1130 |
rs397861580 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235802220 | AAAAAAAAAAAAAAA[-/A]CTAGCAGTACTGGGA | 1130 |
rs397939210 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845648 | CGGCAGTTAGGGGGG[-/G]ACACGGTGGGAGTGA | 1130 |
rs397939532 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235770058 | GATGGAAAAAAAAAA[-/A]GAAAAAAAGTCCCAT | 1130 |
rs397952914 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235805638 | CAATAATATATATAT[-/AT]TACATATATTATGTA | 1130 |
rs397983337 | in-del | -/AAAAA/G/GAAAA | 1.65091e-05 | 0.00287303 | intron-variant | LYST | GRCh38.p7 | 1:235755432 | GAAAAGAAAAGAAAA[-/AAAAA/G/GAAAA]AAGACAAAAGATTCC | 1130 |
rs398089970 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235869797 | GCCTACAGAGCTCTA[-/A]CACCATCTGGCTCCT | 1130 |
rs527239913 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670057 | CTTTCTTGCTCTGTA[C/T]ACAGGCCCCACCCCT | 1130 |
rs527268817 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235692500 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGG | 1130 |
rs527287814 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235694334 | TCTTTTTTACAACAT[-/A]AGTATGATGTTCTCT | 1130 |
rs527293296 | in-del | -/A | 0.415891 | 0.18703 | intron-variant | LYST | GRCh38.p7 | 1:235744606 | ATATTAGAAAAGTGG[-/A]AAAAAAAAAAATGCT | 1130 |
rs527296133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235692104 | TTGGGAGGCTGAGGC[A/G]GGAGAATCACCTGAG | 1130 |
rs527297992 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235743152 | GGTTTACCATAGAGT[A/G]TTCCCTAACAATTAA | 1130 |
rs527301379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698121 | GTTTTATCCTCTACT[A/G]AACTCTTCTTTTTTA | 1130 |
rs527316548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235840394 | TACAAAATGAGAAAC[A/G]GGAAAAGTGAGGATG | 1130 |
rs527334182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782209 | TTGGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 1130 |
rs527341210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790742 | CTTTTCAATGAACAG[C/T]TTTTTTTCTGCCCTA | 1130 |
rs527351077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841353 | TTTTTTAAAGAATTG[C/G]AAGAACCGTATTTTT | 1130 |
rs527358906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738229 | TTAGAACACCAAAGA[C/T]TGTCTCTGGCAAAGA | 1130 |
rs527384023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852758 | AATCAACTTTCAGAG[A/G]GTTAAACGATCTCTG | 1130 |
rs527395541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235826206 | AAACATAGTACAACT[A/G]CTTTGCAAAACAGTT | 1130 |
rs527401972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833391 | TTTTCCTCTTAATGT[C/T]ATGTTCATTCCATTA | 1130 |
rs527429892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879260 | AATATTAGAGCATTT[A/G]TCACTGGGGAGAATA | 1130 |
rs527442836 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700792 | AAATGCTGAGTGTCT[A/T]TTATATGCCCAGGAC | 1130 |
rs527471028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704082 | TCCAACAAAGGACAT[G/T]ATCTTGTTCTTTTTT | 1130 |
rs527473962 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235816475 | AAATAAAAATAAAAA[-/T]AAAAAAGCCATACTG | 1130 |
rs527492630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767186 | CCAGTGGGTAGCAGC[C/T]GGCCTCCAGATTAAG | 1130 |
rs527498521 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661526 | CATGTGTATGCAGTT[C/T]AAGGTTAAAGCATAC | 1130 |
rs527507929 | snp | C/T | 0.000126654 | 0.00795683 | intron-variant | LYST | GRCh38.p7 | 1:235712014 | ATTACAAAATAACCA[C/T]AAGCCCTCAGAAATA | 1130 |
rs527518897 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235863120 | GAACTTGGCCCAGCA[-/C]GGTGGCTCACGCCTG | 1130 |
rs527535531 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235704923 | AATAGTGCTTTTCAA[A/C]ATTCTGTGGTATTCA | 1130 |
rs527549045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796952 | ATATCCACCAGGATA[C/G]ATATAATTAAAAAGG | 1130 |
rs527559345 | snp | C/T | 6.6212e-05 | 0.0057534 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804632 | GGGAAAGATGGTCCC[C/T]CATTTCAAATAATAT | 1130 |
rs527573071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744242 | TACTGGTAAAAAATA[C/T]TGTATTTAATTACTA | 1130 |
rs527589860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752723 | CTGGTCTTCAATCTT[A/T]ATCTTGATAATCTAC | 1130 |
rs527596491 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845256 | CTGGAGAAGTTTCTG[A/G]CCTTACCTGAGCTGA | 1130 |
rs527599511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235875435 | AATTACAGGGATGCT[A/G]ATTAAGCATTTCATA | 1130 |
rs527614752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235760422 | TCTTGCTGTTATTAG[C/T]GAGAATAGTTTCTTT | 1130 |
rs527646392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235877594 | TATTTTTAGTAGACA[C/T]GAGGTTTCTCCATGT | 1130 |
rs527664540 | snp | A/C | 3.31153e-05 | 0.00406898 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773872 | TATCTTCCAGTCAAG[A/C]AATAGTTCCTCTAAC | 1130 |
rs527669193 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235781200 | ATAAAGCCTCAATTT[C/G/T]GAAATTGGTGTAACG | 1130 |
rs527679405 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792786 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 1130 |
rs527684434 | in-del | -/T | 0.485528 | 0.0838238 | intron-variant | LYST | GRCh38.p7 | 1:235839264 | TATATATATATACAG[-/T]TTTTTTTTTTGAGAC | 1130 |
rs527739128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836687 | AAATAGAAGTGTTCC[C/T]CTGAAACCATTTCTC | 1130 |
rs527743905 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869032 | GCTACTGCAGTATGT[A/G]TTTTATTCAATAGTA | 1130 |
rs527749508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710796 | GGCCATGCAGCCTCT[A/G]TTCGTCTCCCTCTTG | 1130 |
rs527751872 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235720131 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 1130 |
rs527788011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728323 | TTTACCTCTTTGTGT[C/G]TTAATTTCTTTATTA | 1130 |
rs527809107 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235818165 | TATTACAACTTTTTT[A/T]AAAAAAGAAAGAAGG | 1130 |
rs527832424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742665 | TTACCAAAGGCTCAA[A/G]AATTATAAATTAAAA | 1130 |
rs527837279 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827671 | TTCACTCCAAAGGCA[C/T]ATCTACTGTTCCTAC | 1130 |
rs527862845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690949 | TGAGACAGAGTCTCG[C/T]TCTGTTGCCCAGGCT | 1130 |
rs527872684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786902 | TGGGGCCTGTCGTGG[C/G]GTGGGGGGAGGGGGG | 1130 |
rs527874300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845728 | GCTTTCCCCCACTTC[A/C]CTGACAACCTTCATG | 1130 |
rs527891291 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235734050 | AATATTAAAATAAAT[A/G]AACCATCTAAACAAT | 1130 |
rs527897854 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772138 | GCTGAGGTAGGAGGA[C/T]CACTTGAACCTGAGA | 1130 |
rs527911495 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235837596 | TGAGCCACCGCATAC[C/G]AGCCTGGGTAAGAGT | 1130 |
rs527916956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846270 | AGACCCAGAAGAGAG[A/G]CAACAATCACTGCAG | 1130 |
rs527920472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803266 | TTAATACCTCAAAAA[A/G]GGGGTTTCTAACAAA | 1130 |
rs527952019 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768926 | GGCCAAGAAAGGCAA[C/T]AAAATGTTTTTGTGT | 1130 |
rs527984393 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235707286 | CCTGAAGAGGTAAGA[-/T]TTTTTTTTTTCTAAA | 1130 |
rs528006258 | snp | A/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884812 | TTTTTTTTTCATTTG[A/T]GACAGGGTCTTGCTC | 1130 |
rs528027371 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235668669 | ACTTTACAAAATTCA[A/T]CTCCCTCAGGATCAG | 1130 |
rs528067441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235868996 | CACCGCTCCTGGCCT[C/G]GGTTCCAGTATTTTA | 1130 |
rs528102141 | snp | C/T | 0.000399281 | 0.0141238 | missense | LYST | GRCh38.p7 | 1:235709230 | ATGAGGATAAAAAGA[C/T]GAGGATCATTACGCG | 1130 |
rs528104140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717920 | TCACTCTGGAGTGAA[C/G]TGGCGTGATCTCAGC | 1130 |
rs528105558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235764482 | ATTTACTACATTTCT[C/T]TTTTTTTCTTTTCTT | 1130 |
rs528105590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235773075 | TAATCCCAGCATCTT[A/G]GGAAGCCGAGGCAGG | 1130 |
rs528111130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860618 | GTTTGCCTTTTTTCA[C/T]TTAGTGATATGCACT | 1130 |
rs528161551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802658 | TCACACTAGAATATA[C/T]ATGAAATTGGGGACT | 1130 |
rs528162651 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235758737 | AAACCACAATATATA[-/T]TTTTTAAGTGCTACT | 1130 |
rs528187758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749949 | GATAATTAACTAAAA[C/T]CAGAGATCTAGAGAT | 1130 |
rs528233122 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660592 | AAATGAAAGTTAGGC[C/T]GGGCGTGGTGGCTCA | 1130 |
rs528255607 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235732613 | AAGGACAGCTAATAT[A/C]CTGCGGTGAATATTA | 1130 |
rs528264091 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883259 | GCAACCGTCTTCCCA[C/G]GTAGCTGCAACGAAA | 1130 |
rs528271314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682037 | ATTACGAAGATTTAA[C/T]ATGTGGCTCACGTCT | 1130 |
rs528271906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778874 | TCTTGTCTTTTTTCT[C/T]TTTTTTTTTGAGACA | 1130 |
rs528291883 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235727184 | CTGGAGTGCAGTGGT[A/G]TGATCTCGGCTCACT | 1130 |
rs528298793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235875581 | GCTGATGGAAGGAGT[C/T]CTGCCCCACACAACT | 1130 |
rs528301379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797887 | ATCTGATAAGAAATC[A/C]ATATCCAGAATATAT | 1130 |
rs528309234 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235692551 | ATGCCTGGCTAATTT[A/T]TTTTGTATTTTTAGT | 1130 |
rs528317910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724738 | GTCTCTATAGTTTTG[C/T]CTTTTCCAAAATGTC | 1130 |
rs528332854 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734122 | ATAAGTTAGAGTAGA[A/C]TGGTTAACCAGGGTT | 1130 |
rs528336726 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235717051 | CTACTATCCTTCTTT[C/G]CCTTACTTCTGCAGC | 1130 |
rs528372547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235729390 | AAACTAAAATGCTAT[C/T]CATGTGCTTTTCAGA | 1130 |
rs528375873 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235763505 | GCCCAGGCTGGAGTA[C/T]GGTGGTGTGATCTTT | 1130 |
rs528388540 | in-del | -/GTT | 0.23208 | 0.249357 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715134 | TGTCAGTCCTAAGTT[-/GTT]GTTGTTGTTGTTGTT | 1130 |
rs528395462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815415 | TTAGACAGGCTATTT[A/C]GGATGGGCTATTTGA | 1130 |
rs528443594 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235719875 | AATAAAGAGAAAAAA[A/T]ACACATAAAAAATAA | 1130 |
rs528444430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772455 | CTACTAGAACCCTGC[C/T]ACACTTAGAGCAAAC | 1130 |
rs528461918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793812 | CAAAAACAACAAAAA[A/C]CACTTTTCTTTTTAT | 1130 |
rs528465654 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235757885 | GCTATTGGAAATGTT[-/T]TTTTTTTTTTTTTTC | 1130 |
rs528470720 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885486 | AAAAAGATTCATATC[A/G]TAACATCAGGTGGAG | 1130 |
rs528486707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695018 | CTAACTTTCATCTGT[A/G]AGCTACAACATTGTT | 1130 |
rs528498830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235801166 | AAACTTCATTAATCA[C/T]TTAGAAGATCTAGTG | 1130 |
rs528502771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694309 | CTTGAGCCACTGTGC[C/T]CAGCCCTCTCTCTTT | 1130 |
rs528516723 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235696214 | AGAACTATGGCCCAG[C/G]TAGCATACCTAATTT | 1130 |
rs528526435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689072 | CTAGCTGAATTTTCT[C/G]AAATCAAAGAATTAA | 1130 |
rs528536134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785501 | TAAAAATAGGTTAAT[C/T]TGTGTTAAGGGTATA | 1130 |
rs528592540 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235667369 | TAAACACACATACAA[-/C]CCCCCCCAGAAATCA | 1130 |
rs528613219 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, synonymous-codon | LYST | GRCh38.p7 | 1:235740644 | TGGTGCTGTAGAATA[A/G]TCTATACAGATTTCT | 1130 |
rs528647541 | snp | C/T | 0.000149505 | 0.00864467 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762819 | GCCTCAGGTACATGA[C/T]TGACCGCACTTTCTC | 1130 |
rs528655543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866814 | GGAACCTTCTGCCGG[C/T]AGCGTCGGCGCCCGG | 1130 |
rs528671719 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235814837 | AGAAAACCCTTCACG[A/G]CAATGATTCCTGTTG | 1130 |
rs528674341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665463 | AAAAATACAAAAAAA[A/T]TAGCCAGGGGTGGTG | 1130 |
rs528718534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858236 | AGGTACTTCGTAGCT[A/G]TGAGTCTTGGGAAAA | 1130 |
rs528721264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859699 | CCTTAAAGCCTGCTT[C/T]GATTCCTCCCTCTCC | 1130 |
rs528721294 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829151 | GAGGTTGCAGTCAGC[C/T]GAGATTGCACCACTG | 1130 |
rs528753605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700128 | AACCCAAAACCATAA[A/G]AACCTTAGAAGAAAA | 1130 |
rs528775233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814434 | CAAGAATGAAACTCC[A/G]GACTTTAAAGACTTA | 1130 |
rs528804356 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235707402 | GAGGCTGAGGTGGTG[C/G]ATCACGAGGTCAGGA | 1130 |
rs528811863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807114 | ACACCACAGCCACCA[C/T]CACACCTGAGGTGGA | 1130 |
rs528813746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763456 | CCAGGTTCTACTGAC[A/T]TTTTCCCTTTTTTTG | 1130 |
rs528816835 | snp | A/G | 2.20306e-05 | 0.00331885 | intron-variant | LYST | GRCh38.p7 | 1:235755697 | ATTAAAATTAAATAT[A/G]ATATATACAAATCAG | 1130 |
rs528850782 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670915 | AAATAACCCTAGTAA[A/T]ACAAAAACTACAAAG | 1130 |
rs528858603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881490 | TACATATCAAAGAGC[A/G]AAAGCAGGATCTCAA | 1130 |
rs528867747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784461 | TTTATGGTTCCTCTA[C/T]CTGTCAGCTGACATA | 1130 |
rs528880987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819802 | AAGTGCCTGCCACCA[C/T]GCCCAGCTAATCTTT | 1130 |
rs528895541 | snp | A/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854169 | GATTAATTACTACAC[A/T]TCAGGCACTATTGTA | 1130 |
rs528904321 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235669449 | CAGATGGGAAATTGG[A/C]TGTCTGCAACCAATC | 1130 |
rs528923326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235731314 | ATGTTTATATATTTG[A/G]TCAGGGAATGCATAT | 1130 |
rs528943245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827831 | TATGACTTAAAAGAG[A/G]AAGTATTCTATTTAC | 1130 |
rs528965934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723634 | GGTTACCGATGACCC[C/T]GACGAGAGTGGTGAG | 1130 |
rs528976699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828289 | AAGGGATAGGGGAAC[A/G]ATAGCTAAAGGGTAT | 1130 |
rs528980964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820355 | ATGGAAAGCTAATAG[A/G]TATTTCTTTTCTTTT | 1130 |
rs528990751 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861714 | TGCCCAGGCTGGACT[C/T]GAACCAGGCTCAAGC | 1130 |
rs529001912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235722944 | AACAGTATGGATGCA[A/G]GAAGGCCAGTTAGGA | 1130 |
rs529004618 | snp | A/G | 1.68744e-05 | 0.00290463 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777067 | GTGATTCTTACCCTG[A/G]CAAAGAGAAAAACAA | 1130 |
rs529005148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672772 | ATTAAGAGTCTGAAC[C/T]GCTCACTAGAAAGAT | 1130 |
rs529010447 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235745895 | GCTGGGGGTGAGAGG[A/G]AAGTGGGTGTGGCTA | 1130 |
rs529013596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680894 | GTGAGCCACCGCGCC[C/T]GGCCTACAAGTGATT | 1130 |
rs529019151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873439 | AACTCAAACACTAGA[A/C]AAATACACAATATAC | 1130 |
rs529082568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791053 | CTTTGGGAAGCTGAG[A/G]TGGGCAGATCACCTG | 1130 |
rs529090215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849584 | GTCAAACTTTCACTG[C/T]TTGCTGATGATATGA | 1130 |
rs529108704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235829787 | CAAGCTAAAGGACTC[A/G]GTAATTATTAGTTCA | 1130 |
rs529110980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698788 | TGAGGCAGGAGAATG[G/T]CATGAACCTGGGAGG | 1130 |
rs529120777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841518 | GGAAATGGGCAAATG[C/T]TACACATTAGGGTCT | 1130 |
rs529134522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235798674 | TGATTAGAAAGAGAA[C/T]TAAAGTGCTGAAACA | 1130 |
rs529147705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824272 | ATCCACAGAGTGCAA[C/T]AGGTATGGAAATTAT | 1130 |
rs529149075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235842083 | TCTAATAATAGACAG[C/T]GCAGACTGTTATCAC | 1130 |
rs529158726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799119 | ATAATAAAAATACAC[C/T]CATATACTAAATAAG | 1130 |
rs529161437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693593 | CATAGCAGAACATAT[C/T]ATTTGGTGCAAGACC | 1130 |
rs529184814 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235834510 | CCCAAAGTACTGGGA[G/T]TACAGGCGTGAGCCA | 1130 |
rs529194906 | snp | G/T | 0.000331939 | 0.0128786 | intron-variant | LYST | GRCh38.p7 | 1:235762870 | GAATCCAAATTTTTT[G/T]TGAAACAGCAAAATT | 1130 |
rs529206353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738433 | GGATATCTTTGACCT[A/G]TAGTGGCTTGGAAGA | 1130 |
rs529224125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235823428 | TTGCATTATTCTCCT[A/G]TTGAAACAACTCTTG | 1130 |
rs529248534 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235872093 | CGGAAGTCAGGAGTT[C/T]GTGACCAGCCTGGCC | 1130 |
rs529258443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235671209 | TCCCAAAGCGTTGGG[A/T]TTACAGGTGTGAGCC | 1130 |
rs529260333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663275 | CAAGTTGAGATGCTC[A/G]TAAATGCGGTGATAT | 1130 |
rs529264297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864157 | AATTCCCATTTTCTC[A/C]TGCTGTATTCGGAGT | 1130 |
rs529275596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235768685 | TATGGAAATCTCAAA[A/G]TTTATAAGTGCCACT | 1130 |
rs529293155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722086 | ATCATTAGGATTTCT[A/C]AGGAGAAAAACATTC | 1130 |
rs529295601 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235767934 | CCCCCTCTGCCGACC[C/T]CTGGCTTTCACTTTA | 1130 |
rs529306869 | snp | C/T | 0.00177792 | 0.0297624 | intron-variant | LYST | GRCh38.p7 | 1:235755475 | AGGGAAGAACACACT[C/T]ACTCTTCATCAAGGC | 1130 |
rs529325488 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761102 | CATTTATTTAAAAAA[A/T]ATTTTTTTTAAAAAG | 1130 |
rs529343008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705644 | TCCTGCCTCAGTCTC[C/T]CAGAGCATTTGGGTT | 1130 |
rs529357709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713673 | GGGATACAGCTAAAC[A/G]TCCTACAATGCACAG | 1130 |
rs529363365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235753781 | ATATGTGGTGATATA[C/T]GTCCTCTTTTCTTCT | 1130 |
rs529386635 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235722292 | GTGACATGAAAGTGA[C/T]TGAAGGATTCTGAGC | 1130 |
rs529398835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705100 | TGGTTTTATTATTCA[C/T]ATTTGACAAGTTTGT | 1130 |
rs529399975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761425 | CTATTCTTTTCTTCT[A/G]TAAAGTAGCGATGAG | 1130 |
rs529444924 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674354 | TCTAATCCAATTAGC[C/T]ATCCCTTTCACCCTG | 1130 |
rs529447027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728456 | TATTTATTATTACCA[C/T]TATTCTTACATTACT | 1130 |
rs529450480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235664119 | CTAAAAAGCCCTCTA[G/T]ATTTGTTTATTTGTT | 1130 |
rs529467336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692370 | AACCAACCAACCTAG[C/G]TGCTATCAGTCTGAC | 1130 |
rs529481351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677777 | AAAGAAATTAAAAAA[A/T]TTTTAATTCCTCATA | 1130 |
rs529485716 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235832215 | AAGTCTGCTGAAGCA[A/C]TGACAATGTGAAAGT | 1130 |
rs529511767 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235879148 | AGCACTGGGATTACA[A/C/G]GTGTGAACCACCACT | 1130 |
rs529522786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235825942 | TTATTTTTATAAAAG[C/T]CACAGTAATCTAGAC | 1130 |
rs529529367 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705635 | AAGCGATCATCCTGC[C/T]TCAGTCTCCCAGAGC | 1130 |
rs529588133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678432 | GATACTCAGCAGTTA[C/T]GGCTTGACTTTCTAA | 1130 |
rs529591099 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235703493 | TAGTGTCATTATCCC[A/G]TAGAGTCAGATGGAG | 1130 |
rs529618832 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235875363 | AATCACTTATTGAAA[A/T]ACCTCAAAGCACATG | 1130 |
rs529632944 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235871344 | AGGCCGGATAAAAGC[A/C]AACCTGCTGTGTTAC | 1130 |
rs529636642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697696 | AACCTCACTCAGCTA[C/T]GAGCTCCTTGAAGAG | 1130 |
rs529662598 | snp | G/T | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759510 | TTTGTGATTGCGTTA[G/T]TAGTGAAGAAGTAGG | 1130 |
rs529675083 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695352 | GGCAAGGATGCAAAA[C/T]TCAGGAACTGCCTGT | 1130 |
rs529677403 | snp | A/G | 0.000399281 | 0.0141238 | missense | LYST | GRCh38.p7 | 1:235697212 | AGACCACAGGTACTG[A/G]AGCACTGGGGGAACC | 1130 |
rs529689180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235703973 | GTCCATGAGTTCTCA[C/T]TTAGCTTCCACTTAC | 1130 |
rs529702071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235797669 | TGTAAAACTATATAT[A/G]CCTAAGAATAAAACT | 1130 |
rs529719022 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235847542 | TGAATGGAACCATAC[C/T]GCACATTTCAATGCT | 1130 |
rs529722608 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235733110 | ACACCAAAGTCACAT[G/T]AATAAGTTATCTTAA | 1130 |
rs529743856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831607 | CTTAGTTCCTGTTCA[G/T]CCTGGGACCTCACAG | 1130 |
rs529754799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840201 | GGCAAATCAATATAT[A/G]GGGTACTATGTACTG | 1130 |
rs529757583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235788864 | TAAGAAAAAGATGTT[A/G]GAATGATCAGTAAAA | 1130 |
rs529781787 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235730098 | AATTTATCAAATACA[G/T]TTTTAAAAAAGCCTA | 1130 |
rs529790603 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235737205 | TCAACTGCACTCAGC[A/G]GGATTGTTATTAGTG | 1130 |
rs529793934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669277 | CATGCCCACCTCCTG[A/G]TGAGGCAGGAGAATA | 1130 |
rs529809969 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698687 | CCATCCTGGTTAACA[C/T]GGTGAAACCCTGTCT | 1130 |
rs529847075 | snp | C/T | 1.79187e-05 | 0.00299317 | intron-variant | LYST | GRCh38.p7 | 1:235744195 | CAAAATTAGTCATAT[C/T]ACTGCTATCTTGCCA | 1130 |
rs529848533 | snp | A/C | 7.15948e-05 | 0.00598266 | intron-variant | LYST | GRCh38.p7 | 1:235773812 | CATTTTACCACAATA[A/C]AAAATGGAAAAAAAG | 1130 |
rs529851613 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235816739 | CGATGGAACAGAATA[A/G]AGAGCCCAGAAATAA | 1130 |
rs529861898 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235870455 | TGTCACTTTCCTTTT[G/T]CTGTCCATAAATCTC | 1130 |
rs529869172 | snp | C/T | 0.000116662 | 0.00763658 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766243 | GATCTACAAACCTCT[C/T]GGGGCATGGGTGTGA | 1130 |
rs529873388 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235869852 | CCCATCACTACCTAC[A/G]TACCTGCTTCTTTAC | 1130 |
rs529899503 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841023 | CACGTGTGCAGAGTC[C/T]GCTGTCAGGGCAAAA | 1130 |
rs529901193 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235872099 | TCAGGAGTTCGTGAC[A/C]AGCCTGGCCAATGTG | 1130 |
rs529917460 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662234 | TTTTAAGTAAAATTT[A/T]TATGAAGAAACAGAA | 1130 |
rs529937838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818057 | TCTTTCCAGAAATTT[A/G]TCATTTCATGATTAT | 1130 |
rs529960390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719080 | CTGGGGTGCAGTGGT[G/T]CAATCTCGGCTCATC | 1130 |
rs529971077 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810175 | CCATAGCATCTGGAG[A/G]AGTCTGTTCTTTGGT | 1130 |
rs529977103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235766670 | GTCTATGTGAGTAAT[A/G]CTAGTGCTACTTTAT | 1130 |
rs530002049 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235883985 | TCAGAGACAAGGTTT[C/T]GCTCTGTCATCCAGG | 1130 |
rs530010604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751086 | AATAGTTTCCTTCAG[A/G]AAAAAATCTTTCTTA | 1130 |
rs530030817 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235784501 | AAGGCTGCAGGGGCA[C/G]TAAAGCATAGGGTTT | 1130 |
rs530032806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235819818 | GCCCAGCTAATCTTT[C/T]CGTAATTTTAGTAGA | 1130 |
rs530034435 | snp | C/G | 3.30671e-05 | 0.00406602 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759057 | CAGTGTTTCTATCAA[C/G]AAGACTTGGCCAACG | 1130 |
rs530040591 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884647 | TTGTGCTAAAATATG[C/G]CTTTTTTTTTTCCTC | 1130 |
rs530073296 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235856725 | TTTAAATAAGGCTAA[C/T]AGAGAAATATTTCAA | 1130 |
rs530077873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838184 | TGCCAGCTGAGAGTG[A/T]GAAGTGGGAAGGAGG | 1130 |
rs530114677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866157 | GGTCTTCTCGGGTAA[C/T]TTCCCAGCTTATTTA | 1130 |
rs530137010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690880 | TTGCAGCAGCATACT[A/G]TATATTTACATGGTA | 1130 |
rs530158259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736084 | ATATCAAAGGAAACA[C/T]ATGATTTTCTTAAAC | 1130 |
rs530197848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831006 | GATTAAGGGAAATAA[A/G]CTACAGCAAACAGAA | 1130 |
rs530199699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727338 | CATGTTGGCCAGGCT[A/G]GTCTCAAACTCCTGA | 1130 |
rs530199963 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235718349 | TTTTGTATTTATCTG[G/T]GCAAGCATATTCACT | 1130 |
rs530200552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749354 | ACACATATAAAGTGG[C/T]ATTTTGCAAACTAGA | 1130 |
rs530219691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852032 | ATAGCAGTTGTTTAG[C/T]GCCCAGGCCCTTCTT | 1130 |
rs530251509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877532 | CTGCCTCTGCCTCCC[A/G]AGTAGCTGGGATTAC | 1130 |
rs530258655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845141 | CTGCAGGCCCCAGGA[A/G]ACCCCCAAATACTGT | 1130 |
rs530324376 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235672699 | TTTCTAAACTTAATT[-/A]AAAAAAATTAATTCT | 1130 |
rs530342427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852671 | GAGGTAAGTGACAAG[C/T]TGATTGACAATAAAG | 1130 |
rs530349615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701520 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 1130 |
rs530358928 | snp | C/T | 0.000272665 | 0.011673 | intron-variant | LYST | GRCh38.p7 | 1:235741645 | TAAAATCAATCAAGA[C/T]AGGAATGAATTAGGA | 1130 |
rs530378924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814648 | TGCCCCTTAACTAAC[A/G]GCTTTAATGGAGTGA | 1130 |
rs530381931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795274 | AGGTCCCAAACCTGA[G/T]AACTCTTCTCTAAAT | 1130 |
rs530411966 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867363 | AGGATGAAGATAGAA[G/T]AAATAACGGGAAGGA | 1130 |
rs530422237 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835338 | AGCTGCTCTGACTAC[C/T]ACCACCCTCCAGCTT | 1130 |
rs530449469 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868325 | ATAATGAGCACCTAC[A/G]ATGCGCTAAGTATTG | 1130 |
rs530471754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235725241 | GAGTTCAAGACCAGC[C/T]TGGCCAACATGGTGA | 1130 |
rs530476198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822970 | TGCAAACTCAGATGT[A/G]AGACCAGCTGATACC | 1130 |
rs530476547 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235666859 | GCTAGAAGGCTCATT[A/G]AAGTCACTGGAAACA | 1130 |
rs530504482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772319 | GGGAATAACCATTTT[A/T]AAAAAATTCTAAAGG | 1130 |
rs530512563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875492 | TCCAGAGTGGCTGGT[G/T]GAGAGTCTGTTTTAA | 1130 |
rs530532419 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235716929 | TTTTGTAACTAACAG[A/T]CACCATTCAAAATTA | 1130 |
rs530563149 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873712 | CTATCTTAATTCCCA[A/G]TATATTCCTGCGGTC | 1130 |
rs530577988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732464 | GAGCCACTGTGCCTG[A/G]CCTGCCTTCCATATT | 1130 |
rs530591228 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235790347 | TGGTCATGCTACTTA[A/C]CTTCCTCTAAAAATA | 1130 |
rs530601495 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722590 | TCCCAGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 1130 |
rs530619099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815339 | AATTTCAGATATAAT[A/G]TTGTGCTATGAAGGA | 1130 |
rs530623377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688381 | AATCTCCCAAGAGGA[C/T]AATCTAATATGTGAA | 1130 |
rs530627712 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235882413 | GACTTTATTCCATAG[G/T]TACTGGGCAGCTACT | 1130 |
rs530641874 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235767213 | TAAGGGTATGGGAGG[A/T]AAAATTCCTCATCTT | 1130 |
rs530656417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835954 | ATACAACAATTGTTA[C/T]AATGTCATAACAAAG | 1130 |
rs530671962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764292 | TTTCTTTATCCTCTT[C/T]CCCTCAACTAGGCTG | 1130 |
rs530702053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724682 | CCTACTCATCCCTCC[C/T]TTCCTCTCCCCAATC | 1130 |
rs530709417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785236 | CCCTGATCCACCCAT[C/T]GTAAGTGTCAAACTC | 1130 |
rs530712500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689002 | TAATAATAATAATAA[C/T]AATAATAATAATAAT | 1130 |
rs530727540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829781 | TGTATACAAGCTAAA[A/G]GACTCAGTAATTATT | 1130 |
rs530732260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725327 | TAGTTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 1130 |
rs530746879 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235726500 | TGCATGAAATACATC[C/T]GTATGGGTCAAAAAG | 1130 |
rs530749082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784690 | TAAATCAGGTAATCT[G/T]TATAAAGTGCCTAAT | 1130 |
rs530756849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793770 | TGAAGAAATAGCAAT[A/G]TAACTAAATGTAAAT | 1130 |
rs530761690 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235874485 | TAAAAAGCTTCTTGG[A/G]AAGCAGCCTCTAAAC | 1130 |
rs530770614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235666890 | TAGCCATAAAAGATA[C/T]TGAGGTAGGGGTTTC | 1130 |
rs530809805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235800216 | CAGCCTCCCAAAGTG[C/T]TAAGATCACAGGCAT | 1130 |
rs530838507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850391 | TACACATGTACTAAG[A/G]ACTTAAACTTAAGAC | 1130 |
rs530845070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699541 | CTGCAATAAACATAC[A/G]AGTGCATGTGTCTTT | 1130 |
rs530853992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235733213 | AAATATATTTTTCTC[A/G]ACCATCCTGTTTCAG | 1130 |
rs530864647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681981 | GTTTCAGTAGTCTCA[G/T]GTAAAAATGGAGATA | 1130 |
rs530869737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235694261 | CTCAAGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 1130 |
rs530870400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792960 | TGAGCCATGGCGCCC[C/T]GCCTTAGATGTTCTC | 1130 |
rs530872464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843645 | TGTGAGGAAAATGAT[A/G]TTCTGTTTCATAACG | 1130 |
rs530878501 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235707674 | AATTCTACTTCTAGG[A/G]ATTTATCTTAAGGAA | 1130 |
rs530879530 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235747534 | AGTCACTTTTGAGGC[-/A]AAAAAAAAAAGAAAA | 1130 |
rs530880297 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235841034 | AGTCTGCTGTCAGGG[A/C]AAAACCACTCCACAC | 1130 |
rs530882954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882973 | TTCTCCCTCCTCAAA[C/T]ACTCTTCCCTGCGGT | 1130 |
rs530905179 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739882 | AGAAGAAAAAGTCAA[C/T]GACAACCACAGTTAA | 1130 |
rs530917656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858155 | TGACCCCTACTTTGC[A/C]GAAGGCTAGCATGGT | 1130 |
rs530938868 | snp | A/G | 1.65737e-05 | 0.00287864 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762796 | GGACCTTCCTCCACT[A/G]CTGGAATGCCTCAGG | 1130 |
rs530941922 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235744361 | AAATTTGAAAATGCA[C/T]GTCATACAATTCCAA | 1130 |
rs530957304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820269 | CTGCACAGGCAGATG[G/T]GCACCAGATGGCTAG | 1130 |
rs530968944 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235672733 | AACTCGATTACCATG[A/G]ACTAAGTGTTTTCCC | 1130 |
rs530991669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769581 | AATTGTCTAATATAC[C/T]AACCAAGCAGATATT | 1130 |
rs530999775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872625 | TTTTATGGCCAGCTT[A/C]TATTCAGAAAGTTGG | 1130 |
rs531018718 | in-del | -/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235792445 | TCAGCCTCTGGAGTA[-/G]CTGGCATTACAGGCA | 1130 |
rs531023190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235776429 | CGAAGATGGCATTCC[A/G]AGGATGAAGGAAGAT | 1130 |
rs531031090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235671922 | TTAGGTTATTATAGT[A/G]TTCTAGGTAACAGTT | 1130 |
rs531083544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706718 | TGAAACTATATTATT[C/T]TCCTTTTTTAGAATG | 1130 |
rs531104755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694553 | CCCAGAAGTAGATGA[A/G]TATAACAAATAAATA | 1130 |
rs531118205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714525 | GAAGTAGTTCAAGAA[C/T]GGTTGAGTAAAAGAA | 1130 |
rs531135839 | snp | A/G | 9.91326e-05 | 0.00703964 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806135 | TGTGACTTCTGAACA[A/G]TTTCTGTATTATCAT | 1130 |
rs531153896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680319 | GCAGTGTAGTGGTGT[C/G]ATTATAGCTCACTGT | 1130 |
rs531155246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665381 | TTTGGAGGCCGAGGC[A/G]GGTGGATCACCTGAA | 1130 |
rs531168039 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235844769 | GAAGGGGACCAAAGA[C/G]GGGGAGGGGGAAACT | 1130 |
rs531169281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738284 | GCTGGTCACTATCAC[A/G]GCTGAGGCACATCGC | 1130 |
rs531178941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722779 | ATGAGCCACTGTGCC[C/T]GGCCCTGAGCAAGTT | 1130 |
rs531182768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857679 | TGTGGGTGTGTGTGC[A/G]CGTGTGCACACAGGT | 1130 |
rs531186594 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848402 | CTAAGAGGAAAGTTC[A/G]CAGTCCTAAATGCCT | 1130 |
rs531190966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866618 | GGCTGTCAAAGGCGG[C/T]CCGGCGCCGCGAGAA | 1130 |
rs531197394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782937 | TTTGATTAGTCTCTT[C/T]TGCTTCATGGATAAC | 1130 |
rs531208979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715089 | AGAATTCTTTTTCCT[G/T]TAGTTTGATTAGTCT | 1130 |
rs531226416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693075 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 1130 |
rs531234398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790835 | AAATTTATTCTAATG[A/T]TGGAGAATGGCTGAT | 1130 |
rs531279890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770390 | CGCAACAATTTAACA[G/T]TGTGTATATATTCAG | 1130 |
rs531323679 | snp | C/T | 3.3745e-05 | 0.00410748 | intron-variant | LYST | GRCh38.p7 | 1:235791649 | GCTCAAGGAAAATTA[C/T]AGTCTGAAAACAATC | 1130 |
rs531342024 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235760037 | TTGACTGAATGATTC[-/AA]AGTCATTAGGATTAA | 1130 |
rs531354837 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235871259 | TTCTCTACTAAATCA[-/C]CAATAGCATTTGAAA | 1130 |
rs531367926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761313 | TAAAGACAAGACTAG[A/G]TTGGACTGACAATAA | 1130 |
rs531378063 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235833628 | TATCATTTGGACTCA[C/T]AAACTAGATGAAACA | 1130 |
rs531396141 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780945 | AAATTTCTTTATTAA[C/T]ATATTTGGAGTAGTC | 1130 |
rs531399854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864724 | ATCGCTTGAGCCCAG[A/G]AGTTTGAGACCAGCC | 1130 |
rs531408025 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235760520 | TCATTGTAGTGCATG[C/G]GATACAAGTGCATGC | 1130 |
rs531411588 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826921 | CTCCAGGCCTCAAGT[A/G]ATCCATCTACCTCGG | 1130 |
rs531434497 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235745224 | TTACCACTTTTTTTT[-/A]ATGTGTGATGAGAAC | 1130 |
rs531458094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235730325 | TTCTTCATTTAATAG[A/G]TGAGGTAACTGAGAC | 1130 |
rs531467569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687394 | TTGAGTGTGAATGTA[C/T]GTGTACTTCACATAT | 1130 |
rs531468683 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYST | GRCh38.p7 | 1:235798570 | GCGACAAGGGCAAAA[C/T]CCTGTCATAAAAAAA | 1130 |
rs531505208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745736 | TTGATATATGCAACA[A/G]CCAGAATGACTCTCC | 1130 |
rs531524453 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817479 | TAAATACCCATCAAC[A/G]GTAGACTGGATAAAG | 1130 |
rs531524834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235705565 | TAATTTTTAAATTTT[C/T]TGTAGAGACAGGTTC | 1130 |
rs531528691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753742 | GCTAAGTATTTTGTG[C/T]CTCATTTTCCTTATC | 1130 |
rs531529829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698290 | AAACTTGCTTATGTC[A/G]TTTTCCAAATAAATG | 1130 |
rs531534033 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824792 | TTTGGGTGGCTGAGG[A/C/T]GGGTGGATCACGAGG | 1130 |
rs531572216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804677 | AGTTCTAAGGTAAAA[C/T]AAAAGAGACTAAGAA | 1130 |
rs531587890 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775026 | GGTTGTATTTAATTA[A/C]TGAGAGTATAACTCG | 1130 |
rs531591410 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235698698 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 1130 |
rs531591931 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235755953 | ATAGAATATTTGTAC[C/T]TAATGCTGAGAGGGA | 1130 |
rs531593847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878965 | GGTGAGGTCTGGGCT[A/G]TTAGAGTACCCATCA | 1130 |
rs531619168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871171 | TTAATGTCTTCATTA[A/G]GTTGTTACCAACATC | 1130 |
rs531637532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805250 | GGTTTTAGGAGAAGT[C/T]TCGTCCCAGCCTCAT | 1130 |
rs531642805 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235729251 | TATTTCTTATGGACA[C/G]TTATATCTGATAAAA | 1130 |
rs531651367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851537 | AAATACCACCTGTAC[A/C]CCAATAACTGATGGA | 1130 |
rs531666386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745166 | ATACATTGTCAAATA[A/T]TCACCATAATCAAGC | 1130 |
rs531683628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712755 | TCTGAGCTAAAGAAT[G/T]GAGTAAAATTTCCTG | 1130 |
rs531688364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818268 | TAGGCAGTGTCAGAT[C/T]TAATGGGCCCTTGTG | 1130 |
rs531693939 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235663166 | TGAGGTTAGTGTAAA[G/T]AAGTTATCTTCAGTG | 1130 |
rs531701960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819046 | CACCAAGTGAGTTAG[C/T]TCTTGCAAACCATGG | 1130 |
rs531749478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774495 | AATAAAAATGAGCAC[A/G]AATATCTGTGACTTG | 1130 |
rs531750244 | snp | A/G | 0.00237359 | 0.034368 | intron-variant | LYST | GRCh38.p7 | 1:235782131 | CAATGACTTTAGGAA[A/G]TCTAGTACTAAGTAT | 1130 |
rs531751117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736263 | TTAAACATGAATCCT[C/T]AGAAAATAATAAAGT | 1130 |
rs531753632 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752317 | CAGTATTTATTCATG[C/T]TTATTCTATGGCAAG | 1130 |
rs531757899 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711073 | CTGACCAATTTCTTA[C/T]TTCTGACCAATAAAA | 1130 |
rs531759512 | snp | A/G | 1.65198e-05 | 0.00287395 | intron-variant | LYST | GRCh38.p7 | 1:235677437 | ATAGTAAAAATGGAT[A/G]TATTAAAAATGCTAT | 1130 |
rs531779745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235720230 | TATATGTTCAGAGAT[A/T]TAGCAACCAAACATG | 1130 |
rs531780017 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809397 | ATTTTCATCACACTA[C/T]TTATTAGGGCTTTCA | 1130 |
rs531785950 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844635 | TATCCAGAACCTTTA[C/T]TCAAGTCCACTGGAT | 1130 |
rs531787204 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884895 | ACGCCTGGGCTCAGG[G/T]GATCCTCCTGCCTCA | 1130 |
rs531821234 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235699733 | CTCCACAGCCTCACC[A/G]GCATCCATTGTTCCT | 1130 |
rs531828623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839314 | CAGGATGGAGTGCAG[C/T]GGCATGATCTCAGCT | 1130 |
rs531839350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796777 | CTTGGACTTTCAGTC[A/T]CCAGAACTGTGAGAA | 1130 |
rs531868233 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235810805 | CTATACTTACTCTAA[A/T]CACTAGCTGACATTA | 1130 |
rs531868707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728392 | CTATGGAAATTAAAT[C/T]AGAATATATGCAAAA | 1130 |
rs531877663 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662527 | GAGTATTTCATGGCA[A/G]TAAACTTTTAAAATA | 1130 |
rs531898860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235832117 | GCTTTCTTGATCTTA[C/T]CAGATGGTATCAGCA | 1130 |
rs531902265 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884080 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 1130 |
rs531906642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737054 | ACTGGAAAAAAAAGC[C/T]TACCTACCTATCTAA | 1130 |
rs531945274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685189 | TCAAGTGTAACTTAA[C/T]AGGCTCCCTGATGTC | 1130 |
rs531950080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235691326 | GAGGAAAGAAACTCA[A/G]GTTTGGAGAGATTAA | 1130 |
rs531962781 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235857721 | CACACACACACGTAT[A/T]TATACACAAACATAT | 1130 |
rs531986089 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661304 | TCGGTTTTTAAAAAA[A/G]GATGAGTAGCAACCC | 1130 |
rs531993949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235781394 | TCTTGGTAAACTCCA[C/T]TTCTAACTAAAATTT | 1130 |
rs532009617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831530 | GTAAAAATGAACCAA[C/T]GGGATACAAAGAGAA | 1130 |
rs532047083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846475 | AGGCTCTTCAACACC[C/T]CCCCAAAATTTCTCT | 1130 |
rs532049867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802786 | TCAATAAAAAGATTA[C/T]GCAACACACTTGTTA | 1130 |
rs532073982 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772656 | TTGCTTAATTTGTAC[C/T]TACGATGAAGCCTTG | 1130 |
rs532080727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878195 | GCCCCAAGGCAACAT[A/C]CCTGGAGCAGGTGAG | 1130 |
rs532097220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751703 | TTTAATAATTACCAT[C/T]AAAGAAAACTAAAGG | 1130 |
rs532110495 | snp | A/C | 1.65592e-05 | 0.00287738 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759014 | TTTGGCTCATAACCA[A/C]GAGAATAGGCAAAGT | 1130 |
rs532147208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235758331 | GCTGAAGAAATACAA[C/T]GCCTAGGCAATGTCT | 1130 |
rs532162815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853674 | TCTTGGTTAACATGC[C/T]ATTCCGGCTGCCTTG | 1130 |
rs532195391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675313 | TCTCGCAAACTGCAT[A/G]TTTATCATAGTTAGA | 1130 |
rs532197285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683053 | CATAGAGTACAGATT[C/T]ATTGACCTATTCTCC | 1130 |
rs532226148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772558 | AACAACCCTATACTC[A/C]TTCCCTGACTGGGTC | 1130 |
rs532231677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743545 | AAATGAACCCTGACA[C/T]TTATCAGTATTCTCT | 1130 |
rs532260333 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750992 | ATTGTATCTCCAATA[G/T]TTAGCACAATGCTCA | 1130 |
rs532261953 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235762121 | TAAAACTTAAAGTGT[A/G]ATTATAAAAAAAAAA | 1130 |
rs532271238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719024 | CTGAGTCCTTTTCTA[C/T]TTTTATTTTTTGAGA | 1130 |
rs532292729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669239 | TGATTGAGGACTGAA[A/G]CTTCCAGATACCCCC | 1130 |
rs532298003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235816654 | CATCACATTACTTGA[A/C]TTCAAACTACTCTAT | 1130 |
rs532298017 | snp | C/G | 1.66344e-05 | 0.0028839 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808787 | TCCACTGCTGGGCAG[C/G]ATCCCTTGAAATCTG | 1130 |
rs532310208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235773218 | CAGCTACTTGGGAGG[C/G]TGAGGTAGGAGTATC | 1130 |
rs532342918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773671 | GGGTACAAAGTTTTG[A/G]TTTTACAAAACAAAA | 1130 |
rs532350040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692928 | TGGGAAGCTGAGGGA[A/G]GAGGATCACTTGAGT | 1130 |
rs532354709 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235779746 | GGCCCTTACTACCCA[A/G]TAATTATTGACAACC | 1130 |
rs532363419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235795122 | AGAGCAGTAAGAAGC[C/T]GAGCTGTCCATCTAA | 1130 |
rs532369824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235869071 | CATCGATACTAAATA[C/T]ACATATCAAATAAAA | 1130 |
rs532372085 | in-del | -/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662574 | TATATAAACAATCAA[-/C]CAACCAATTTAAATT | 1130 |
rs532384028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823682 | ACTACTTGTAGTTCA[C/T]TGAATGTGCTGTGTT | 1130 |
rs532405925 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235869787 | CTTACAATTGGCCTA[C/G]AGAGCTCTAACACCA | 1130 |
rs532421725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235694740 | AACCACATATCATGA[A/G]TCTTGAGTCCTCTCA | 1130 |
rs532451349 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235778973 | CTAGGTTCAAGCGAT[C/T]CTCCTGCCTCAGCCT | 1130 |
rs532478657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829917 | GACATAAGATACAGG[A/G]ATATAAGATTATGTC | 1130 |
rs532512679 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235823218 | GATAGCACCACTGTC[A/G]AGTGGTTAAGATTTC | 1130 |
rs532531468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756532 | GCGAGCTCAATACTA[C/G]GTTGTATTGCAAGTG | 1130 |
rs532533443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764215 | CATATGCTCTATGCT[A/G]CCAGAAAACAAAAAT | 1130 |
rs532546831 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235721051 | TAACATTAATGGGTA[C/G]AGAACTGAGATTCAA | 1130 |
rs532555546 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235695522 | ACTGTAGTGGCACAA[A/C]TAAGATAGGCTTAGA | 1130 |
rs532556900 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235800010 | CACCCAGACTGGAGT[A/G]CAGTGGCATGATCAT | 1130 |
rs532558397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235807218 | TACTTTAAATCTATA[A/C]CTTATGAAGGGAAAG | 1130 |
rs532569397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763607 | AGGCATGTGCCACCA[C/T]GCCCAGCAACTTTTT | 1130 |
rs532584437 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235845602 | GGGGAAGTTTTCAAG[C/G]CCATCTAGCCCTCAG | 1130 |
rs532587238 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235786808 | GCAAGGACAAAAAAC[A/C]AAACACCGCATGTTC | 1130 |
rs532589441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235858812 | TGGGGGTGGGGAAGG[A/G]GAGTGGTCCAAGTTC | 1130 |
rs532624236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837449 | CCTGGGCAACATGGC[A/G]AAATCCCATCTCTAC | 1130 |
rs532628324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235734854 | GACAGAGGATTAATG[C/T]TAATTTTGTTAGATG | 1130 |
rs532636881 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235725391 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 1130 |
rs532647346 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235833542 | AAGCCTTCAAAATCA[C/T]GTTGATGGTTAATAT | 1130 |
rs532649424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695042 | CATTGTTCAGTCAAT[A/G]CCTCTCTAGAATGTC | 1130 |
rs532683739 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235831125 | TTTCATCTCTGGGCT[A/C]AAAGTAATTTTGAGG | 1130 |
rs532684328 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235883842 | TCCTATGAGTCATAA[A/T]TCCCTGATTCTTCTG | 1130 |
rs532692084 | snp | C/T | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757354 | TCTGCTTGAATAAGC[C/T]TGTCCATCACATCTT | 1130 |
rs532693428 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235740767 | CTGACATAGATATTC[G/T]TAAACAAGCTTTTTT | 1130 |
rs532695723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801366 | GATAGAGATTTAACA[C/T]ATCCCATGGACACAA | 1130 |
rs532713685 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235863003 | TTGTAATTTTGTCTT[C/T]TGACATTACAAAGTA | 1130 |
rs532720103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748674 | GCAGGCAACTTGGAA[A/C]TGCTGAGCAGAAGAA | 1130 |
rs532724648 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846411 | CTCTGACAGAGCCTA[C/T]CCAAATGAGAAGGAA | 1130 |
rs532746145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700680 | TCACCGTGGTTCAAA[G/T]AAAGAAAAGCAGTGG | 1130 |
rs532746265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708934 | TGTTTTTAAAGAGAG[A/G]AAATATAAAACCTGA | 1130 |
rs532750695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873643 | CTATTATTGAGCATA[A/G]TTCTTAGCCAGGTGA | 1130 |
rs532767527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770726 | TTTTAGAGCAAATCA[C/T]ACTAAATTGAAGAGT | 1130 |
rs532783424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708345 | AAACATGGTGCCATT[G/T]TAAAGTAGAACATGT | 1130 |
rs532794239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825808 | ATCCTAGTGTGCATT[C/T]TGTAGAAATAACAAG | 1130 |
rs532805452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801934 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 1130 |
rs532838873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807705 | GTTTATAAAATTATT[G/T]TTAAATGCACCAGAT | 1130 |
rs532859987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235845077 | ACTGCAAGAACAAAC[C/T]AGCAATCCCGAGAGG | 1130 |
rs532888072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715414 | TCCAGGCAACGCTAG[A/G]AAAGTGCTGGATGTT | 1130 |
rs532918185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681873 | CTGTGTAATTTTTTT[C/T]AGTTCATTAATTCTG | 1130 |
rs532925811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882321 | GTGATGACAGTCCTG[C/G]ACTCTTGCAGGTGAT | 1130 |
rs532947822 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785868 | CAGGCTAAAATTTGA[C/T]ATTAAGATATTCCAC | 1130 |
rs532955646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850326 | TCAGCTAGCCGCATG[C/T]AGGAGAATGAAACTG | 1130 |
rs532956967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235842247 | AGGAAAATAAATGTT[A/G]ATAGACAAGCAGAAA | 1130 |
rs532974333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785194 | CTTCAGGTCTCAGGT[C/T]TAATACCCTGTTCTT | 1130 |
rs532975516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235699968 | TCTTCAACAAACCTG[A/G]TAAGAACAAGCAATG | 1130 |
rs532983375 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235757802 | TGGCTAGTGCTGACT[C/G]TATTAGACAGCATGA | 1130 |
rs532992609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829223 | AAAAACCATAAACCT[A/G]CAAATGTCCTGAAAA | 1130 |
rs532996932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693628 | TTAAATCTCTAAAAT[C/G]GAACAATTTTTTAGT | 1130 |
rs533006093 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235799386 | AGGGAAAATAGTAAC[C/T]TTACAATAGAGAAAC | 1130 |
rs533007941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715905 | GATTTTTCACTACTC[C/T]TATCTTCCCATCATA | 1130 |
rs533032801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732329 | TTCTTTTTTGACAGG[G/T]TCTCATTCTGTTGCC | 1130 |
rs533047480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724534 | GATGAACCAATATTG[C/G]TACAATTTTTCTTAC | 1130 |
rs533088206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771304 | TAGTTCAAATATAAT[C/T]AATTACGTAAGAAAA | 1130 |
rs533115451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812840 | CCTAAATAATTTTTC[A/G]TATTTAGTATGAATA | 1130 |
rs533145436 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235706669 | TTTTTCTCCCTTACA[C/T]ATTAATATTATATGT | 1130 |
rs533154179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783927 | CTCTGTCACCCAGGC[C/T]GAAGTGCAGGGGTGC | 1130 |
rs533163895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716257 | TTAATTTCACAGAAA[A/G]AGGTAATTCATTTTA | 1130 |
rs533182874 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235800101 | AGCTAGGACCACAGA[C/T]ATGCACCACCACACC | 1130 |
rs533209922 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765561 | AAACTGTATTTATGG[C/T]ATTATTTCTCACTAT | 1130 |
rs533265872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746669 | AGAAAGGAAAGAGTG[A/T]TTAAGAGAAAATGAT | 1130 |
rs533293302 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789346 | ATATTCCCTGGTGAG[G/T]AGTTTTTGCATATAA | 1130 |
rs533301460 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235680607 | AAGTGATTTTCTTTT[C/T]TTTTTTTTGAGATGA | 1130 |
rs533301856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754523 | AGCCACCACGCCCAG[C/G]CTCACCTGTCTTTTC | 1130 |
rs533310801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235679519 | CTTTTTCATAAATTT[A/G]TTTTCTTAGCTGTAT | 1130 |
rs533311249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665260 | TATGATTGAAAATAC[G/T]TGGAAAGCTAAACAG | 1130 |
rs533323305 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235789667 | ACCATGACCGATGTT[-/A]AAAAAAATACTCCCT | 1130 |
rs533337806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762083 | ACATATGTAACAAAC[C/T]GGCACATTGTGCACA | 1130 |
rs533342319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775788 | AACTGGAAGTTCACA[G/T]TACATCTAGGAAGCT | 1130 |
rs533366808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235761471 | AATTAGGAAGATAGA[A/G]AAGTACTGTAGGCTT | 1130 |
rs533375054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769497 | TATTACTGATCTCAT[C/G]GAGTATCTGTACTTA | 1130 |
rs533376783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672536 | TAGAAAAAAGCAACT[G/T]TGGCTGCTTTTTAAG | 1130 |
rs533378217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782809 | ATGTCATCTATGAGG[C/T]CTTTGAAAACTAATC | 1130 |
rs533385602 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235835914 | AATTTTAAATCTAAC[-/TT]TATCACTATAATTTC | 1130 |
rs533388796 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235714441 | AAACATAGGAAAGCC[C/G]CTTTTATAGACCAAT | 1130 |
rs533404040 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235878367 | CATTGAACTCAGCTT[A/C]TCCTGAATTCTATGT | 1130 |
rs533414510 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235713829 | GAGATGAAAGTGAAT[G/T]GAGACTGAGGTAGTC | 1130 |
rs533442809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235664271 | TTTATAGTTAACATA[A/C]AACTTCAAAACTGTG | 1130 |
rs533458759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722155 | TGCCTGACATTCAAG[G/T]CATGGATGGAGTAGA | 1130 |
rs533465601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820176 | ATTCAGAAGTAGAAG[C/T]GGTGGGATGGGAGTA | 1130 |
rs533520883 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235842196 | TCCTTATGGCCAAAA[A/C]TGAGACACAGACTGG | 1130 |
rs533549521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235839604 | TTCGAGACCAGCCTG[A/G]CCAACACGGAGAACC | 1130 |
rs533551016 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235881099 | AGGGCTGGAACTGGG[C/G]TTCCTAACTCCAAAT | 1130 |
rs533585828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872154 | TACAAAAACTAGCCA[C/G]GCATAGTGGCACATG | 1130 |
rs533588992 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235775242 | AGGCTTGTGAATAAA[C/T]AAAACTGAGAGTAAG | 1130 |
rs533603243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774757 | AATGATGAAAAGAAC[C/T]AGAAGAGTATCTTAG | 1130 |
rs533605885 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235730103 | ATCAAATACATTTTT[A/T]AAAAAGCCTAGTATT | 1130 |
rs533616807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825098 | TTACAGAATAAAAAA[C/G]AAAAATCATATGATA | 1130 |
rs533618719 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235663303 | TATAGAATAAAATCA[G/T]GATCACAAAGCTCAG | 1130 |
rs533623866 | in-del | -/AAA | | | intron-variant | LYST | GRCh38.p7 | 1:235685856 | GTCTTAAAACAAAAC[-/AAA]AAAAAAAAAACAAAC | 1130 |
rs533643723 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235710576 | AAATGATATGATATA[A/C]GCTGTAAAAAACTGT | 1130 |
rs533643869 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235674486 | TCCACAAGAGGTGCT[A/C]AATGAATTTAAAGCC | 1130 |
rs533657050 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868381 | AACAAAAAGAGGAAG[C/T]CAAACTTAACCTGTT | 1130 |
rs533665514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235728796 | TCTCCATCCTTGTGA[C/T]GGTGGGGCTCAGTCC | 1130 |
rs533737004 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736115 | GCTTAAGTTGTTTCT[A/G]ATATCTCATTTTAAT | 1130 |
rs533737033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697319 | TTTAAAAGGTGGTAA[A/G]TGTAGAATTACTTCT | 1130 |
rs533738529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877705 | GCCACCGCGCCTGGC[C/T]GGTCAACTTTCTTTT | 1130 |
rs533770573 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235774270 | ATTGAATTAATCTGC[G/T]ATTAGGCTTTAAAAC | 1130 |
rs533776340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235878413 | CTCTCCCTTCTATCC[C/T]ACTCTCCCTGATTCC | 1130 |
rs533779219 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795525 | CAAGCCCTATATGTG[A/G/T]AAGATGCATTTTTCT | 1130 |
rs533788820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803521 | TTTTCAAAGGGATTA[A/C]TTAAAAGATCTCAGA | 1130 |
rs533805253 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235788466 | GTGCTGGGATTACAG[C/G]CATGAGCCACCACAC | 1130 |
rs533810232 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235784744 | GCTCAAGAAATTGAG[C/T]GGAGAGTGCCTAGGA | 1130 |
rs533813783 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235780731 | TTTTTTCAGAAAAAA[A/T]CATAATTCTAAGAAA | 1130 |
rs533846333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235816727 | AGACACAGAGACCGA[C/T]GGAACAGAATAAAGA | 1130 |
rs533849945 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235850356 | GGATCCTCATCTCTC[A/C]CCTTATACAAAAAAT | 1130 |
rs533901150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719654 | AAAGGAAAATATATA[C/T]AAAGCTCACATCACC | 1130 |
rs533919610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870887 | TAATTTTGGAGCTGG[A/T]CAATCTTAATGCCTA | 1130 |
rs533921631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235700323 | GAGAAAATTTTTGCA[A/G]TCTACCCATCTGACA | 1130 |
rs533928936 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763330 | TCTAAATCCGAATCA[C/T]CTTTTTGCCCTAAAT | 1130 |
rs533946101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235764721 | TTGGTCAGGCAGGTC[C/T]TGAACTCCTGACCTC | 1130 |
rs533958275 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235846098 | TTAAACCACCAAAGC[A/T]AAGGACCCTCACGGA | 1130 |
rs533962913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676259 | TCAAGCTGGTCATCT[C/G]CTGAGGCTTTTCATT | 1130 |
rs533976541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235718482 | TGAGTAGTTGGTCTC[A/G]AACTCCTGACGTCAG | 1130 |
rs533976614 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235750704 | TATTTGATGACATTC[-/T]TCCTTATTTAATATC | 1130 |
rs533978570 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773883 | CAAGCAATAGTTCCT[C/T]TAACAGCTTAACATC | 1130 |
rs533987451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235800732 | TGGAATACCACTTGT[A/C]GGTATTCACCTGAGG | 1130 |
rs533998925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846786 | AAGAAATTCAGAGCT[C/T]GAAGACAAGGTCTTC | 1130 |
rs534003251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235703133 | TGGTCTCACTGAGAT[C/T]AGAAGTATCAATGTT | 1130 |
rs534051530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839065 | TCTGGGCTCAAGTGA[A/G]CCTCCCGCCTTGACT | 1130 |
rs534074491 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660829 | TGGGAGGCGGAGGTT[A/G]CAGTGAGCTGAGATC | 1130 |
rs534093693 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235780177 | TTGGGAGGCTGAGAC[A/G]GGAAGATCGCTTGAG | 1130 |
rs534106725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743718 | CTACTCTTTTCTGAT[A/G]CTGATCTTACTAAAC | 1130 |
rs534127359 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693190 | GGCGTGGTGGCAGGT[A/G]CCTGTAGTCCCAGCT | 1130 |
rs534131934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235875941 | ATGCTTTTTCTTGGC[C/T]GGGCATAGTGACTCG | 1130 |
rs534142645 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667480 | ATGATCAGGAGGAAT[A/G]AGCTTGACAATGTAA | 1130 |
rs534142793 | snp | C/T | 0.000263813 | 0.011482 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810102 | AAGGCAGCTGGCTCA[C/T]TTAAAATGTCAGTGT | 1130 |
rs534147856 | in-del | -/TTCCT | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739121 | TGGGAAAAACATCAA[-/TTCCT]AAGGTTAGAAATAGG | 1130 |
rs534174963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772711 | TAACTCCTGGCCAGC[A/G]TGGCTCCCCTAGTTA | 1130 |
rs534179442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235869336 | AATTAGCCGGGCGCG[C/G]TGGCGGACGCCTGTA | 1130 |
rs534201766 | snp | A/G | 9.96979e-05 | 0.00705968 | intron-variant | LYST | GRCh38.p7 | 1:235830432 | TGACCGAGCTATAAA[A/G]TAAGTATTACAAAAA | 1130 |
rs534228593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709741 | TTTAATAAATTTAAG[A/T]TTATATTTAGTAAAT | 1130 |
rs534250796 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235760366 | TTACTAGCCTAAACA[A/G]CCCTAGACAGTTCTC | 1130 |
rs534258504 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727644 | TTAATATCAGTCTGT[C/T]TAGAATAATAACAAT | 1130 |
rs534267876 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868769 | GGCACAGTCTCGGCT[C/T]ACTGCAACCTCCGCC | 1130 |
rs534273568 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235730772 | ATGGCATTATATAAA[A/G]TAAATATTACATAAA | 1130 |
rs534336592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844942 | AGCAATAACCATCAG[A/T]ATGATTCCTAACTAA | 1130 |
rs534338813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852153 | GTGGTCTCCAGTTCC[A/G]TAGATACTAACATTG | 1130 |
rs534344689 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235763179 | GGGAGATTGTTCATC[A/C]TTGAGGAAAGGACTG | 1130 |
rs534351208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235758515 | GGAATGGAGCAGCCA[C/T]CCTATGACACCTGTT | 1130 |
rs534372558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235845214 | CCTGAACACACACCC[C/T]CACTGGAGAAGCTGA | 1130 |
rs534386816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785771 | TACATTACAGTTTCG[A/G]ATTCTCTATCTTCTT | 1130 |
rs534390639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682502 | CTGATGCAGGAGAGG[C/T]CATGAGCCAGGTGGG | 1130 |
rs534396078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779169 | ACCGTGCCTGGCCGA[C/G]GGTACCACTTCTCCC | 1130 |
rs534405637 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235682138 | AACATAGTGGGAGCC[C/T]GTCTCTAGAAAAAAA | 1130 |
rs534407598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690230 | CTGCTCATAAATTTG[C/T]GTCAGTGTATTTTGA | 1130 |
rs534410275 | snp | C/T | 6.6024e-05 | 0.00574523 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733655 | TGCAGCTATTTTAGA[C/T]ATATCCTTTGATTTT | 1130 |
rs534430125 | in-del | -/AAC | 0.0229672 | 0.104671 | intron-variant | LYST | GRCh38.p7 | 1:235825032 | TCTCAAAAAAAAGAA[-/AAC]AACAACAACAACAAC | 1130 |
rs534433714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786425 | AGAGGATGTGGAGAA[A/C]TAGGAACACTTTTAC | 1130 |
rs534454912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749475 | GAGATACCATAGACC[C/T]GGGATGAGTAGATGT | 1130 |
rs534487375 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867019 | CCGCTCGTCTGCGCG[A/T]GCGCCCTTGGCTCCG | 1130 |
rs534492955 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235779015 | GGGATTACAGGCATC[C/T]GCCACCATGCCTGGC | 1130 |
rs534503813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762966 | AGATGTTTAAAGAGA[A/C]AAATATATAGCATAC | 1130 |
rs534506873 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235815754 | GATTTCTACAATGAG[A/G]ATTACAAAACATTGC | 1130 |
rs534525334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858502 | CAGAATCTTAAATTG[A/G]GAATTCTCACATCTA | 1130 |
rs534550978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235822452 | ATATAGGGCATATGC[A/G]GAGCAGATAACCTGT | 1130 |
rs534596595 | snp | A/G | 5.14907e-05 | 0.00507372 | intron-variant | LYST | GRCh38.p7 | 1:235806809 | TAAAAAGGTTTAAAT[A/G]AAGAAACATCATTTA | 1130 |
rs534602315 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235684485 | AAGGGGAGCTCAGAA[C/G]ATTAAAGGTAATGGC | 1130 |
rs534626561 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235707481 | TACAAAAATTAGCCA[C/G]GTGCGGTGGTGGGCG | 1130 |
rs534646545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801474 | TACCCAAATCTTTGT[A/G]AAAATAGTAGGCTTG | 1130 |
rs534659981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756087 | TCTATCCTAGACCTC[C/T]ACTTCTAGGCTTCTT | 1130 |
rs534661965 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235731803 | CCTCAAGTGATCCAC[A/C]CACCTGGGCCTCCCA | 1130 |
rs534673590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688586 | GATGTTTCACAATTA[C/T]GAGACTAATCACAAC | 1130 |
rs534675429 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821254 | ACAGTCTGGGCAACA[C/T]GGTGAAACCCCATCT | 1130 |
rs534683575 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235855132 | TTTTCCATATGCCTC[C/T]ATCTTATCACTCACC | 1130 |
rs534702328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235834934 | AAATTTTTTTTTTTT[G/T]AGAGGAGTTTCACCC | 1130 |
rs534729533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828097 | TATTCTTTTAGAATG[G/T]CTAACACTACAGACT | 1130 |
rs534729622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793099 | TTAAAAGACACTAAG[C/G]CACACCAATGGAAAG | 1130 |
rs534733301 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713624 | ATGGGGTGTGGGTGG[C/T]GGTGGTACCACTGGC | 1130 |
rs534736139 | snp | G/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853236 | TTGAAAAGAAGTATG[G/T]ACATTTTAACAAGAA | 1130 |
rs534758166 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852659 | CAACTAATACTGAGG[-/T]TAAGTGACAAGTTGA | 1130 |
rs534763172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828660 | TTAGAGTCATTCCTC[A/G]ATATTTACTATTACT | 1130 |
rs534772420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673119 | TAGACCCATTATACC[C/T]GAGTCAAGAAAGCAC | 1130 |
rs534777976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874639 | AATTTTATCCAAAGG[A/G]CTGTCCTTTATTCTG | 1130 |
rs534782392 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669253 | AACTTCCAGATACCC[C/T]CCAACTCTCATGCCC | 1130 |
rs534788857 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831787 | TTATATATTAATATT[C/G]GTTCTTTATATGCTT | 1130 |
rs534795147 | in-del | -/ACT | 0.00119737 | 0.0244387 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884698 | ATATTTTAATTAAAA[-/ACT]ACTGTCATCTTTTTA | 1130 |
rs534800309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235821546 | TTATCAAATGTTTTT[A/G]ATGAGTCAGGATAGT | 1130 |
rs534818430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673813 | AAACCAAAGTAGTTA[C/T]AATAAAAGTCAAGGA | 1130 |
rs534822242 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867558 | GACTCCTGTTCAAAC[A/C]CGGTTTGTATACAGT | 1130 |
rs534876025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693280 | AAGATGTGTCACTGC[A/G]CTCCAGCTTGGGCGG | 1130 |
rs534916836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754103 | TGTATCCAGGAATTC[A/T]AGGTGAGGGATTTAC | 1130 |
rs534944308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235666937 | CTACCACTACTGCAT[A/G]GCTTAATCCTTCAAA | 1130 |
rs534962360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859084 | AATCTCAGCAGATAA[A/T]CTTGCTTCACAGAGA | 1130 |
rs534969177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740014 | AATTTTGATGGATAG[A/C]AACTTTGCTGAGTAT | 1130 |
rs534992186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799480 | CATAAGTCCTTTTGA[C/T]ATGATGCACTCAAAA | 1130 |
rs535013036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776810 | CTCAATTTAAAATCT[C/T]GTACATTTAACATTT | 1130 |
rs535016449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843779 | AAACAACAAAAAAGG[C/T]TATAATAATGATATT | 1130 |
rs535060217 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841494 | TCATGGTGAGAGTAT[A/T]TCCATCATGGAAATG | 1130 |
rs535069466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769144 | AAAAGACTAATTTAT[A/G]TGGAAAGGGCAGGGA | 1130 |
rs535071605 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235663836 | CTCTTGCTGCTGGGT[C/G]ACGGACAACCCGCTG | 1130 |
rs535080914 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235681293 | AAAGAAAGTGGCACT[C/G]CCAATGTTACTGGGA | 1130 |
rs535098105 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235723969 | AATCAGTATGAGTAT[A/G]GTTACAGTGGCCCAT | 1130 |
rs535100814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775930 | TGAACAAGGTTTATA[A/C]GTTTTAGACTTAAAA | 1130 |
rs535104861 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768644 | TTTTCTAGCATTTTT[G/T]TAAATAATACAAAAG | 1130 |
rs535107489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670963 | GATTCCCTCTGATAA[A/C]CCTCTAAGTCTCATG | 1130 |
rs535109367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235865134 | GTCCTCAAACAAGCC[A/C]AGCACACAGGGCTTC | 1130 |
rs535152056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873851 | AAGAAACATTATCAT[C/T]TGAAATACAGGTTTC | 1130 |
rs535152125 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235819935 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCAATAC | 1130 |
rs535164350 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235774744 | ATGTAATTATTTAAA[C/T]GATGAAAAGAACTAG | 1130 |
rs535182410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812231 | CCTTTAGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 1130 |
rs535193479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746149 | AGTCTGGGCTAGCAT[C/T]GAACACATTCAAAGT | 1130 |
rs535194639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805680 | ATTTTTTATATATAT[A/G]TGTGTGTGTGTATAT | 1130 |
rs535215050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235857704 | ACAGGTGTATATATA[C/T]ACACACACACACGTA | 1130 |
rs535220717 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814202 | AGTGGTATTAGGTTG[G/T]GATAAAGATGATGGA | 1130 |
rs535245797 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235761663 | GGCTAAGGGGACAAG[A/G]AAACTGAGATACTTT | 1130 |
rs535249900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737936 | GGATCTCACTGCCGC[A/G]TGCCCCAACACCCGC | 1130 |
rs535253336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850001 | AAAATACCACTATCA[C/T]TCTTCACAGAATTAG | 1130 |
rs535286993 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235782364 | TTTTTTAGTAAAGAC[A/G]GGGTTTCACTGTGTT | 1130 |
rs535290941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840760 | GAGAAAACTCTAGCT[G/T]CATGAAAACCAATTT | 1130 |
rs535294343 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672789 | CTCACTAGAAAGATA[A/T]CGGCTTATCCCCGTA | 1130 |
rs535326577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775388 | AAGTTAGTCAATAGA[C/T]AGGCTCTGCATTATG | 1130 |
rs535338261 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235745039 | ACCTGAACATTTTTT[C/T]AGAATTCCATTTTGA | 1130 |
rs535374117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235747137 | TCCTCAGACTGAACA[G/T]AGAGGAGTGGCATTC | 1130 |
rs535395178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742563 | GGTTAAAATGGTAAA[C/T]TTTATGTTATATATA | 1130 |
rs535434643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235679866 | ACAGAGGCTGTCCAA[A/G]GACAGTGTCAGTGTT | 1130 |
rs535480327 | in-del | -/CTGTGTTGATTTATTA | 0.131723 | 0.220251 | intron-variant | LYST | GRCh38.p7 | 1:235880417 | TCTAAGTCAAGGATC[-/CTGTGTTGATTTATTA]CTCGGTAAAAGTGTC | 1130 |
rs535485059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722306 | ATTGAAGGATTCTGA[G/T]CAGAGAAAAGATATG | 1130 |
rs535489660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235759959 | TATTTTTATTTTAAC[C/T]ACTTTTTATTAATAT | 1130 |
rs535509187 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790834 | GAAATTTATTCTAAT[A/G]TTGGAGAATGGCTGA | 1130 |
rs535517493 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235736391 | GAGTGATCTGGGTCA[C/T]GGCCAAATGAATGGA | 1130 |
rs535527690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704294 | GGATTGCTGGGTAGA[A/G]TAGTAGTTCTGTTTC | 1130 |
rs535546044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235714174 | GAAACCACAGCAAAC[A/G]AGGATGGCTTAAACA | 1130 |
rs535577963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866057 | AACCAGATAAGAATT[A/G]GCGTTAAGGAAACGT | 1130 |
rs535587535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752820 | AGAAACTAACTTGGG[C/T]CAGTTAATAAAGTAG | 1130 |
rs535588760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697842 | AGAATCTCTAGCCAG[G/T]ACTAGAGAAGAAAAG | 1130 |
rs535621592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686038 | AACCTAAACTTGACA[A/C]ATATCCTCAACTGCA | 1130 |
rs535662768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862727 | CTTGAACCTAGGAGC[A/C]GGAGTTTGCAGTAAG | 1130 |
rs535673101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870782 | CAGTGCCTGGCACTT[A/T]GTAGGCACTCAGTAA | 1130 |
rs535675958 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235749194 | AGAAGAGCTTCAGTA[C/T]TCTGCAGTTTTTGTA | 1130 |
rs535682522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832719 | CTAGCTTTTTATTAT[C/T]ATAAACAAAGCTACA | 1130 |
rs535684201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235692728 | TATAAAGATACCACA[A/G]AAACGTTTACATGGG | 1130 |
rs535684506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685649 | TCAGGAGCTCGAGAC[C/T]AGTCTGACCAACATG | 1130 |
rs535692120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719488 | TTCAAGCAATAATCA[C/T]CAATGGATGAAACCA | 1130 |
rs535713549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235833800 | TAGATCTTAGGAGCA[C/T]ACTAAAAAAATGCCT | 1130 |
rs535717461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826448 | CTAATCAGAAATTAA[A/G]AAGTAGTGAACTACT | 1130 |
rs535727278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721682 | CAAAACCACAGAGAA[C/T]AGAACATCCTAAACC | 1130 |
rs535732079 | snp | C/T | 0.000750729 | 0.0193598 | intron-variant | LYST | GRCh38.p7 | 1:235712237 | ATTAAGACACAAAGA[C/T]CTAATTCTATTTGAG | 1130 |
rs535746379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819601 | TATTTCTAGACCACC[C/T]AATCAAGAGAAATCA | 1130 |
rs535766684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235720407 | TTCTATTTTTTAAAG[A/C]GATGCATACTGTAGA | 1130 |
rs535785214 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235863552 | GTTAAATACAGCAAC[A/G]GACCAAAAAGGTACT | 1130 |
rs535792042 | snp | A/T | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810354 | TTTCTTGCATCTCTT[A/T]CAGAATAGCGATGGG | 1130 |
rs535818126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767362 | CTCAGATTTAAGAAG[A/G]GAACACTGAGTCTAC | 1130 |
rs535864801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848013 | ACAATGAATTTAAAC[C/T]ATACCTTGGAACAAA | 1130 |
rs535866195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235788208 | TCTGTCACCCAGACT[A/G]GAGTGCAGTGGCGCG | 1130 |
rs535867514 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662608 | CTGGTCCTTTTGGAA[C/T]CATAGAAAAAGGGGA | 1130 |
rs535868440 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235846541 | CCCTGATTTACCTGA[A/C]AAAGAATTCAGGAGG | 1130 |
rs535877087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235830494 | TTTTAAAACTATGTG[C/T]TTTTGTTGTTTGTTT | 1130 |
rs535879040 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235691110 | TTTTTAGTAGAGACG[A/G]GGTTTCACTGTGTTA | 1130 |
rs535895067 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235804291 | AGGAAAAGCTTATCA[A/T]ATCACTCTCCTGTTA | 1130 |
rs535903950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838776 | ATCTCCTCCCCAATC[C/T]TGGGCTTCAATTTTC | 1130 |
rs535904549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839759 | GCAGTGAACTGAGAT[C/T]GCGCCACTACACACC | 1130 |
rs535915260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789233 | CTCACACTACCAAAA[C/G]TCATTCTAGAATTAT | 1130 |
rs535919241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698336 | CTGACGTATAGACTA[C/T]CTTTTAAAAAAATCG | 1130 |
rs535924887 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735419 | CCAATCTTTTATTAA[C/T]AGGCCCTAAAACCAA | 1130 |
rs535927193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692226 | TAGTCCCAGCTACTT[C/T]GGAAGCTGAGGCAGG | 1130 |
rs535932178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684495 | CAGAAGATTAAAGGT[A/G]ATGGCAGTGTGAATA | 1130 |
rs535945489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235804785 | TTATTTGCAGTTGAT[A/G]TGAAAGCAAAATGAC | 1130 |
rs535950489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824576 | GCTGGGCATGGTGGT[A/G]TGGTAGAAATATTCA | 1130 |
rs535961155 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235863748 | TGAAATTTTTAACCC[C/G]CTGGTATAGTCAAGG | 1130 |
rs535982309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736376 | TTTAAAGAAGGTATA[A/G]AGTGATCTGGGTCAT | 1130 |
rs535988826 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235730750 | GTTTAGGATTTTTCT[A/G]AAAATGATGGCATTA | 1130 |
rs535988916 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769641 | ATTAGATGATATCAA[A/T]AAAGGCAGAGAAAAA | 1130 |
rs535995710 | snp | C/T | 1.66272e-05 | 0.00288328 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808942 | TTGGTGATATCTCTG[C/T]TCCTCCTAACTGATC | 1130 |
rs535997335 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660706 | AAGCCCCGTCTCTAC[G/T]AAAAATACAAAAAAA | 1130 |
rs536033750 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235766419 | TTACCATTACCATAA[C/G]AACTCATTAAATTGA | 1130 |
rs536043538 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846129 | GTCCACTGCACCCTC[C/T]ACCACCTGCACCAGA | 1130 |
rs536045253 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235669452 | ATGGGAAATTGGCTG[G/T]CTGCAACCAATCAAA | 1130 |
rs536080483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774097 | ATTAAATTCAAAGGA[A/G]AGCTAGTAAATAATT | 1130 |
rs536102606 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872972 | CCAGGTTTATGACTT[A/G]CTTTGTGGTGGAGGA | 1130 |
rs536118687 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235805697 | GTGTGTGTGTATATA[C/T]ATGTATATATATTAC | 1130 |
rs536126221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668443 | ATATATGTATCAAGA[G/T]ACCTTAAAAAAAGTT | 1130 |
rs536128495 | snp | C/T | 1.66056e-05 | 0.00288141 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809765 | CAATTCAGTTAAATT[C/T]TTCCTAAGATTTTCT | 1130 |
rs536167696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702349 | CTGGTCAATCCTTTT[C/G]ATTGTAGATGATAAC | 1130 |
rs536200481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735561 | TGATTCTACTGTGTA[C/T]AGTATGTATTATTTA | 1130 |
rs536209719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743634 | AATGAGAGTAAGTAG[C/T]CATAAATACAGTCCT | 1130 |
rs536220583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683511 | TATAACGAGTCAACT[C/T]ATTCATCATTACCTA | 1130 |
rs536230760 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235835591 | GCAGTTTCATTTTAT[C/G]CAAGATCATAATTCT | 1130 |
rs536269800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772007 | GCGGGAGGACTGCTT[A/G]AGCCCAGGAGTTTGA | 1130 |
rs536271019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779116 | AGGTGATCCACCCGC[C/G]TCGGCCTCCCAAAGT | 1130 |
rs536275804 | snp | A/C/T | 3.29523e-05 | 0.00405898 | synonymous-codon, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787283 | GGTGAGTACTAAATG[A/C/T]TGCCATTTGCTTGGG | 1130 |
rs536309430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780524 | AAGAAAATATAATGA[A/G]CAACATTTTTTAGGA | 1130 |
rs536335514 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235863415 | TCTTTAGTAAAAGGC[A/G]AAAGATTTATACAAT | 1130 |
rs536346129 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885032 | CCCAGGCTCAAGCAA[C/T]CCTCCCGCCTTGGCC | 1130 |
rs536363402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235816031 | GCCACTCAGGAGGTT[A/G]AGGCAGAAGAATCAC | 1130 |
rs536364942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808309 | ATAAAGAGTAAATAC[A/G]ATCACACTGCTGCCA | 1130 |
rs536385322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235869220 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 1130 |
rs536435947 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852359 | TCCTGTACCTCAAAG[C/G/T]CATTTGTGGTAGCTC | 1130 |
rs536437325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235861042 | TAAAGTTCATTCCTT[A/G]TTATTGCTAAGTAGT | 1130 |
rs536454339 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235748740 | CAATAAAATGGTATC[C/T]AACTCCTCTAGCAAT | 1130 |
rs536455471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757916 | ACCAAGGAAGAAACA[G/T]CTTTATTAGGAGTCT | 1130 |
rs536471640 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672726 | TTCTAGAAACTCGAT[C/T]ACCATGGACTAAGTG | 1130 |
rs536476198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852912 | TCCTAATACTGCATA[C/T]AATTTTTGACAGACT | 1130 |
rs536491716 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845594 | ATAGCCTCGGGGAAG[C/T]TTTCAAGCCCATCTA | 1130 |
rs536493749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701804 | CAACACTGTCTACCA[C/T]ATTAATGCTTTAAAA | 1130 |
rs536506237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846042 | CAACCAGCACAAAAA[C/T]AGAGCATTAAAACAT | 1130 |
rs536507450 | snp | A/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235786370 | TCTCACACCAGTTAG[A/T]ATGGCAATCATTAAA | 1130 |
rs536540053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734439 | AATCATTCTTTATCT[A/C]TGATGGAATCTCCTA | 1130 |
rs536548614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822664 | GGTCAGAGAAGAGAC[C/T]ATGGTAGCTTAAACA | 1130 |
rs536573122 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883504 | AGCTTCATGCACCAC[A/T]GAAACCTCGGAATAC | 1130 |
rs536583501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750333 | TTTGATTTAGCATAA[G/T]TTAAACATACTACTG | 1130 |
rs536607951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725559 | CATAACTGTGGGCCT[C/G]CCATCATATAGATTT | 1130 |
rs536614284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875813 | TACTCAAGCCTGGGT[A/G]ACAGAGCGAGACTCT | 1130 |
rs536648643 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739858 | TGGTGACGAAATGGA[C/T]TGAGAAAGAGAAGAA | 1130 |
rs536652668 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868681 | GACTATTATTTTTTT[C/T]GGTACCAGTGTTTTT | 1130 |
rs536660814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235858916 | TGCTTAACCATCCTG[C/T]TGGCCTCTGTACATT | 1130 |
rs536677355 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235822645 | GAGGAATAATAATAA[-/T]TTTGGTCAGAGAAGA | 1130 |
rs536685686 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235797463 | TTCCTCTCAAAAGTC[A/C]ATACCCCTAGCATAA | 1130 |
rs536691545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823281 | TAGGAATGCCAACAT[C/T]CCCTACATCCTCTCA | 1130 |
rs536709670 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792746 | TCAGCTCACTGCAAC[C/T]TTTGCCTCCTGGGTT | 1130 |
rs536717522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235700807 | ATTATATGCCCAGGA[C/T]CTTCCTAGGAACTGG | 1130 |
rs536717622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793339 | TTAAAATATATGCAA[A/G]TAATTGAGTATTTCA | 1130 |
rs536731428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815729 | AATACAGCTAACCAG[C/G]AAGGTGAAAGATTTC | 1130 |
rs536740212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740296 | ATATAATAAAGCATA[C/G]ATATATTAAGTGTTT | 1130 |
rs536754134 | in-del | -/TTTTTTT | 0.491834 | 0.0633738 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884121 | ACCATGCCCAGCTAA[-/TTTTTTT]TTTTTTTTTTTTTTT | 1130 |
rs536763269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717394 | CAAATCTGTCAGTGC[C/T]GGTGTTCACATTCTG | 1130 |
rs536770414 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235829556 | TCATTTTCTACTAAA[A/G]TGAAATAAAGATATA | 1130 |
rs536791187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860291 | CAGCCTCCCCAACTA[C/T]GGACAGCCCCCCTAA | 1130 |
rs536792787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756584 | AGCAAACTAAAGAAA[A/C]ATGAGAATCTTTACA | 1130 |
rs536797634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764593 | CAACCACCGCTTCCC[A/G]GGTTCAAGCCATTCT | 1130 |
rs536807443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723045 | GACTCTCGATGTATT[C/G]TGAGGACAGAGCCAA | 1130 |
rs536808541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872971 | TCCAGGTTTATGACT[C/T]GCTTTGTGGTGGAGG | 1130 |
rs536828469 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235770039 | AGAAGAGAATCTGGA[G/T]AGAAGATGGAAAAAA | 1130 |
rs536841476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844848 | AACATATCAGTTGAA[C/T]TGTACAATATTTAAG | 1130 |
rs536849480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689498 | TGAGAGTGCTGGTAA[C/T]GTGTGTGGAATGGAG | 1130 |
rs536886660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235793958 | CTGCCTCAGCCTCCC[A/G]AGGAGCTGGGACTAC | 1130 |
rs536891915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820482 | TCAGGCGATCCTCCC[A/G]CCCCAGCCTCCCAAG | 1130 |
rs536910320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836924 | CAGGGAAGCTGGAAC[C/T]AGTGAATCAATTTGG | 1130 |
rs536927033 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684197 | CTTCCTCAAAGCTAT[C/T]CTGTGCACAAATACT | 1130 |
rs536968176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235723877 | AGGTCAAAGACAATC[C/T]TCATATAACAAAGGC | 1130 |
rs536974092 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235788105 | TTCAGTATTTGATCT[-/A]AAAATCAAACAGAGA | 1130 |
rs536984841 | snp | A/C | 4.99089e-05 | 0.00499519 | intron-variant | LYST | GRCh38.p7 | 1:235733474 | AAATCTTCATGGAAG[A/C]CAATTTTAACTGACC | 1130 |
rs536986373 | snp | C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235866937 | GCGCACTCCCCACCC[C/G]CGCCCGCCCAGGTAA | 1130 |
rs536992040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762507 | GCTTGATGAAAGACA[A/C]ATGACTATGATAAGA | 1130 |
rs536999402 | snp | C/T | 2.07269e-05 | 0.00321916 | intron-variant | LYST | GRCh38.p7 | 1:235806790 | GTGAAAGAAAAAAAG[C/T]ATGTAAAAAGGTTTA | 1130 |
rs536999484 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680727 | CCTCAGCTTCCTGAG[C/T]AGCTGGAATTACAGG | 1130 |
rs537019684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738717 | GTTGAGAGTGCTTAC[A/G]AGGTGATCAAACTCA | 1130 |
rs537034407 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235879001 | ATAGTGAACATTGTA[C/G]CCAACAGGTAACACA | 1130 |
rs537038312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841770 | GGAGAATTGCAGATA[C/T]AGAAAACAGGTGGAA | 1130 |
rs537055732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712863 | AAGTTTGGACTCTCT[G/T]TTCTGCCAACAATGA | 1130 |
rs537058311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746057 | GGGTCTCTCTCTGTA[G/T]TATTCCTTAACTGCA | 1130 |
rs537059603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666359 | AATAAGCCAGACACA[A/G]ACAGACAGGTACTGT | 1130 |
rs537085022 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235791239 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCTAGC | 1130 |
rs537098008 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235877374 | CATGGGAACACAGAA[C/T]TCATTTTGTAAACAG | 1130 |
rs537112390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834762 | CACACAGCTATCAAA[A/G]CACAGGGTATATTTC | 1130 |
rs537115765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680042 | ACACACACAACTAAG[A/G]CTGAATAAAAATATA | 1130 |
rs537134368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807265 | AAAATCTACGGAAGG[C/T]TCAGCATCACATGAA | 1130 |
rs537145124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235731648 | ACTGTAATTTCTGCC[G/T]CCCGGGCTCAAGCGA | 1130 |
rs537200625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804892 | TTATTTGGTTTTCAT[G/T]GCAGCATGGTAAAGA | 1130 |
rs537214326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881651 | TATATTTACATACAC[A/G]TACATACATATATAT | 1130 |
rs537234209 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235672959 | AGCACAAACTCCACC[A/C]CTCAAACTCCCAGTT | 1130 |
rs537247751 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235724410 | TTAGGTTTACAGAAA[A/G]TTGAGCAGATAATAC | 1130 |
rs537255887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235680671 | TGGCGCAACCTTGGC[C/T]CACTGCAACCTCCAC | 1130 |
rs537262170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856984 | AAATCTCACTCTTGT[C/T]GCCCAGGCTGGAATG | 1130 |
rs537266731 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235776702 | AAGTTTTTTTTTTTT[A/T]AAAGTATTTTTTGAC | 1130 |
rs537268071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663636 | ACTAAGCAAAGAGTA[A/G]CTGATTATTTATCTA | 1130 |
rs537318706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798974 | AACACTGAACTATAC[A/T]CTTTAAATAGGTGAA | 1130 |
rs537319605 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235699029 | AGTTTAAACTTCTAG[A/T]TTTTCAATGACACAG | 1130 |
rs537320266 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235813164 | TCCTTTTTCTTGAAA[G/T]TCTGCATTTGAAAAG | 1130 |
rs537334523 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702047 | TTCATCTTTAAGGTC[C/T]TTTACAACGTCTTTC | 1130 |
rs537348885 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235883885 | ACCTAAGTTTGTCCT[C/T]GTGAGGACCATCATT | 1130 |
rs537356493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698568 | TGTGGGATCCAAATC[C/T]ATCAATATTAAAGTT | 1130 |
rs537369450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813832 | CTGGGACATGGGTAG[C/T]AAAGGATTTAACGAC | 1130 |
rs537434357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775287 | TTCTATAGTCTCTTA[A/T]ATATACTATAGTATA | 1130 |
rs537454215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678018 | TACAACTATCCTTCA[C/T]TGATAGACACTTAAA | 1130 |
rs537478152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842478 | GACAACAGATCATTG[C/T]AAGTTCTTAAAATGA | 1130 |
rs537490050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799421 | CAAACACCTCCTTAA[A/C]CACATGATCAAAGTT | 1130 |
rs537503276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783998 | GATCCTCCTGCCTCA[A/G]TGTCCCGAATAGCTG | 1130 |
rs537506938 | snp | C/T | 1.6519e-05 | 0.00287388 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810063 | AAGTCAAATGGAGAA[C/T]TGTTCATGTTACTGA | 1130 |
rs537520656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687717 | GCTCTCCTGTCCCAC[A/C]TCCCCCACACTCACT | 1130 |
rs537522817 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672324 | GCTAGAGAAGAGAAG[A/G]TAGCAAAAGACAAGA | 1130 |
rs537526266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235712976 | TGTTTCTTAGGAACC[A/G]TATTGCATCATCTAA | 1130 |
rs537541099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235880472 | CACCGTCATAACAGT[A/G]ACTAAACACATCTTT | 1130 |
rs537582302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235670733 | TGTGAATGAGATGCA[C/T]AATTAAGTGCAAAGC | 1130 |
rs537585597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739070 | TATTGTCCTTTTTAT[C/T]TGATCTGTGATTAAA | 1130 |
rs537622904 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235761607 | ATGACAATGGTTAGA[C/G]TGAGGCGAGGTTAGC | 1130 |
rs537629016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864972 | TACTCAAAGAGTGGA[C/T]TCCCCTTTCCACTGA | 1130 |
rs537634194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847769 | CAAAACAAACTTTAA[A/G]GCAACAGCAGTTAAA | 1130 |
rs537639160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782317 | GGGATTACAGGTGCC[C/T]GCCACCAGGCCTGGT | 1130 |
rs537643805 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235742201 | GGCTCACACGTGTAA[-/T]TCCAGCACTTTGGGA | 1130 |
rs537648100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789112 | AGGACAATTGTGGGC[A/G]TAACCAGACCGCTAT | 1130 |
rs537650565 | in-del | -/TCAA | | | intron-variant | LYST | GRCh38.p7 | 1:235701625 | AGAGCGAGACTCATC[-/TCAA]TCAATCAATCAATCA | 1130 |
rs537654059 | snp | C/T | 1.95116e-05 | 0.00312337 | intron-variant | LYST | GRCh38.p7 | 1:235751961 | AATAACAGGTTTGTC[C/T]GTTATACAACTCCCT | 1130 |
rs537659749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761096 | CTATCTCATTTATTT[A/T]AAAAAAATTTTTTTT | 1130 |
rs537665423 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235848733 | ACAAAAGATCATTCA[A/C]GGCTACTACGAATAC | 1130 |
rs537674107 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807898 | TCAATAATCATTTTA[C/T]GTATTATTTTACATG | 1130 |
rs537681255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797203 | AGTAGCAAAAAAGGA[C/G]AACAACCCAAATGTC | 1130 |
rs537684816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235788540 | TAGAATAATACACTA[C/T]TATAAAAGTGGTATT | 1130 |
rs537701917 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235778398 | TTATTTTTCCGAGAC[A/G]GAGTCTTGCTCTGTT | 1130 |
rs537706774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821035 | ATCTTTCCCACATTT[A/G]GCTTTCATATTCCAC | 1130 |
rs537707745 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235781849 | AACTGAGAAAAAAAA[A/C]TGGAAATGTTTCAAA | 1130 |
rs537711938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790015 | TATGATATCGCAGCA[A/T]AATATTCTTTATCTC | 1130 |
rs537755912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706057 | CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 1130 |
rs537768416 | in-del | -/C | 0.0115837 | 0.0752176 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853108 | ACCACAAACTTCTTG[-/C]CCCCCCCACAAACTT | 1130 |
rs537783574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737332 | AGTAAGAAATACAAA[G/T]AAAAGAATCCAAGAA | 1130 |
rs537803292 | snp | A/G | 6.67635e-05 | 0.00577731 | intron-variant | LYST | GRCh38.p7 | 1:235729668 | TCACTCTGTCAAAAC[A/G]TATTTAAAATTACTA | 1130 |
rs537805409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870958 | GAGGAATACAAGACT[A/G]CGATTTCAGCAATAG | 1130 |
rs537825924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862608 | CGAGACCAGCCTGGG[A/C]AACACGGTGAAACCC | 1130 |
rs537832302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668139 | TCAATCTGAGGTTGG[C/T]TGAATCCACGGATGT | 1130 |
rs537843746 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813478 | GAAAAACTCAGAGAC[A/G]ATTTTAAAAGAGAAA | 1130 |
rs537844605 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235730521 | ATACATATATATGGG[-/TA]TATATATATATGTAC | 1130 |
rs537857840 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662846 | TGGTTTGTCCAGTCA[C/T]CCATTTCTTTAGGTT | 1130 |
rs537868578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235774858 | GGAAGACTTTGATGA[C/T]GAGATGAGTATCACT | 1130 |
rs537868603 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235758566 | TCACTTGTCTCTGAT[C/T]AAGTAAGATGTTACT | 1130 |
rs537869071 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235703624 | ATTTAATCAGTCATA[G/T]TGGCTTTCATTACAT | 1130 |
rs537869582 | snp | G/T | 1.75891e-05 | 0.00296551 | intron-variant | LYST | GRCh38.p7 | 1:235766313 | CTCTTTAGATTTAAA[G/T]AATTGTCAACTTAAC | 1130 |
rs537898029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710903 | GCCCACACAGAGAGA[C/T]CACATGAAAAAACAC | 1130 |
rs537912792 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817154 | TTAGAGAAATGCAAA[C/T]CAAAACCACAATGAG | 1130 |
rs537926752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804174 | CCACCATCCCTGAAT[C/T]AGCATTTAATACACT | 1130 |
rs537960082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819882 | CGATCTCCTGACCTC[A/G]TGATCCGCCAGCCTC | 1130 |
rs537988667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864557 | AGTTCCGGATTGGTA[A/T]CCCAGCTTCTGCTCC | 1130 |
rs537990103 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235759895 | AGCTGGGACTATAGG[A/C]ATGCACCCCACACCT | 1130 |
rs537990110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751436 | AACTGATTTTATGTA[C/T]CATGACAATAATGTT | 1130 |
rs538026960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839108 | GGGATTACAGGCGTG[A/G]GCCACTGCACCTGGC | 1130 |
rs538052951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235743820 | GGTGAATTAGCAATA[C/T]ATATTATTCTATAAT | 1130 |
rs538060158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235869367 | GTCTCAGCTAATCGA[A/G]AGGCTGAGGCAGGAG | 1130 |
rs538062636 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235683328 | CATATTCTTCTGCCA[C/T]TCTCAAGTTAGATAA | 1130 |
rs538068487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235877625 | TGGTCAGGCTGGTCT[C/T]GAACTCCCAACCTCA | 1130 |
rs538077111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691652 | TTTGGGGGACACAAA[C/T]AGTGGTAGTTAGGAA | 1130 |
rs538094788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831114 | TTTCAAAATAGTTTC[A/T]TCTCTGGGCTAAAAG | 1130 |
rs538100488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831812 | ATGCTTTCAGAAAGT[A/C]AAAGTATTAAATAAA | 1130 |
rs538132925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728973 | TCTGGACTGAGGCGT[A/G]AGAATGTGCAATTCT | 1130 |
rs538133701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824517 | TAAGTGACTAAAGTC[A/C]CTCATCTAGTTGATA | 1130 |
rs538141904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235719387 | CAAAACATCCTAGGC[C/T]CACCTTGTCTATTTT | 1130 |
rs538143444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832477 | AGAAATGTATGTTTT[C/T]TCCTGATTTAAAAAT | 1130 |
rs538167721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235878494 | AAAAATAATGACGGC[C/T]GCCCTGCTTCCGCCA | 1130 |
rs538169333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727742 | CTTTCTGAAGGCAAA[C/G]GTACTTGATAGTGAA | 1130 |
rs538193441 | snp | A/T | 1.65113e-05 | 0.00287322 | stop-gained, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809629 | GTAAAAGAAGGGCTC[A/T]ATGACGATACTTTGA | 1130 |
rs538195705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235869994 | ATCTCCTCCACGTCT[G/T]TGCTCAAATTTCACC | 1130 |
rs538229370 | in-del | -/CAGT | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235723024 | TGGTAGCAGTGGAAG[-/CAGT]CAGACTCTCGATGTA | 1130 |
rs538238947 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235727927 | TTTAAAATTATATTT[A/T]AAAAAATGTTTGGAA | 1130 |
rs538240866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696458 | TTTGGTGCCCCATGT[A/C]CACAGTAAGTAGGAA | 1130 |
rs538277658 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235837176 | AACTGAGCCCTGGGC[A/T]TAGCATGGCTGAGTC | 1130 |
rs538288704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846893 | ATGTTAAATGACCAC[A/G]CCTAAGAATAATCAG | 1130 |
rs538297699 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235766711 | TAAGGACTAAATAAC[A/G]TAAACTCTTAGAATA | 1130 |
rs538302376 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235688900 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 1130 |
rs538310854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691002 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 1130 |
rs538311551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235796267 | GATAGAATAGACAAA[C/T]AGGACTTCATAAAAA | 1130 |
rs538313678 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235704139 | TATATACCACATTTT[C/G]TTTATCCAATCTGTC | 1130 |
rs538314348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235837861 | GGACATGAGATAAGT[A/G]AGGTTAAAAAAAAAC | 1130 |
rs538318944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235830044 | TAAGATATTTCAGAC[A/G]TTTTGAAAGTATTCA | 1130 |
rs538334127 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235812007 | ATTAAAATACAATAA[-/T]TTTTTTTTTAACCTG | 1130 |
rs538344922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735477 | CAATTGGCCTTTGCA[A/G]CACAGACCTAAACCA | 1130 |
rs538345202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725915 | GGGCCTACACATCCT[A/G]CCATCACTAGGTCCC | 1130 |
rs538348152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803595 | CAGTACTAACTTCCT[C/G]TGTAAGAAAGAAATT | 1130 |
rs538358754 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235804175 | CACCATCCCTGAATT[A/G]GCATTTAATACACTA | 1130 |
rs538360910 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763691 | GTTGAACTCCTGGCC[G/T]CAAGTGATCCACCCA | 1130 |
rs538388763 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235722499 | TGTTTTGTTTTGTTT[C/T]GTTTTAGATGGAGTC | 1130 |
rs538390626 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235742821 | CATATAGCAGTACCC[C/T]CTTACCTGTGGTTTT | 1130 |
rs538398013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807526 | AAAATGTCAGAAAAA[G/T]TTTTAAATGACTGTA | 1130 |
rs538436389 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235676322 | GCCAATGTTTTAGAC[G/T]GAGCTCCTGCACTAG | 1130 |
rs538467358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235779970 | TTCTAGTTGCTATAA[C/T]GAAAAATCCTCACCA | 1130 |
rs538468965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851640 | AGTTCATTAGGAATA[C/T]TATTTTTATATATTT | 1130 |
rs538484242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765782 | TCGGATGAAACCCTC[C/T]GTCCACTGAAATCTC | 1130 |
rs538491963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235708676 | CAGACAACATTTCAC[A/G]TGTGTCATTATGACT | 1130 |
rs538502309 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235696203 | GTGAGCCTAAAAGAA[C/T]TATGGCCCAGCTAGC | 1130 |
rs538512283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701648 | TCAATCAATCAATCA[A/G]TCAAGTGACAGATTG | 1130 |
rs538518507 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845092 | CAGCAATCCCGAGAG[A/G]ACCCACAGACCCTCT | 1130 |
rs538522923 | snp | A/G | 0.000181298 | 0.00951926 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830299 | TACTGTCCAAGGGTT[A/G]CCATGTGCGTCTCCT | 1130 |
rs538555389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701132 | CTGGGGATATATCTG[A/G]GGAGTGGTTATTCCA | 1130 |
rs538560089 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235735347 | AACAAAAGGTGAAAA[A/G]CTCGCAAACCCCACG | 1130 |
rs538569018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801556 | GACTCTGTCTTATTG[A/C]ATATTGCATTTTGGA | 1130 |
rs538583499 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235812112 | CATTTAAAGTTTCAT[A/G]TACTTTATAGACATA | 1130 |
rs538612894 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861803 | GGCTTCGGAGACTGA[C/T]AGACTTTTTATCCAA | 1130 |
rs538615560 | snp | A/C | 6.61081e-05 | 0.00574888 | intron-variant | LYST | GRCh38.p7 | 1:235723994 | GCCCATGAGCACTTA[A/C]ACAATATATATCAAT | 1130 |
rs538621263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690391 | TTTTGTAGACTCATT[A/T]CCAATTTAGTTATAC | 1130 |
rs538641943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673901 | ATGGATTAAATATTC[C/T]GCTCACACCTTAAAT | 1130 |
rs538644165 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235682057 | GGCTCACGTCTGTAA[C/T]GCAAGCACTTTGGGA | 1130 |
rs538674050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785543 | TGGTCTAATCTACTT[A/T]GAGGGATTTTTGAGA | 1130 |
rs538674623 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235835515 | GGGATTTCTCTAATG[A/C]TCTTAAACTGGCATG | 1130 |
rs538682312 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235810685 | CCTTCATTTATGTCA[C/T]ATCTCTGGGTTACCT | 1130 |
rs538703606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787133 | TCTGTTTCAGAAGCT[A/G]TAATTGACTAATGAA | 1130 |
rs538703709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779255 | TTTGCTCTCTAAAAA[C/T]AGTTTTCACATAAAA | 1130 |
rs538718138 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235779564 | TGAATCAGAAGCTCT[A/G]GCCCAGCAATCTATA | 1130 |
rs538760955 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884278 | AGGCGCCCGCCACTA[A/C]GCCCGGCTAATTTTT | 1130 |
rs538780369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715658 | TAACTAATGGCTCAT[A/T]ATGTCTAAGCTGATC | 1130 |
rs538781066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674472 | AATGCTATCAAAGTT[C/T]CACAAGAGGTGCTAA | 1130 |
rs538813154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764504 | TCTTTTCTTTTTTTT[C/T]TTTTTTTTTTTTGAG | 1130 |
rs538817215 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235801465 | CAATTTGCCTACCCA[A/G]ATCTTTGTGAAAATA | 1130 |
rs538840540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688039 | TTGGATCCAATTTTA[A/T]GTTTTCAGTTTCTTT | 1130 |
rs538847382 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235667158 | CATCAACTAAAAGTC[A/T]GAAACCTAGGCATTC | 1130 |
rs538848363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755848 | AATGATGACTCCATC[C/T]TGGAGATCTTAATGT | 1130 |
rs538848871 | snp | A/C | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759011 | TAATTTGGCTCATAA[A/C]CAAGAGAATAGGCAA | 1130 |
rs538854168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763887 | GAGCATCTCATTACT[A/C]TCAAATCCTCACAGC | 1130 |
rs538863624 | in-del | -/CAGTGACTAACTTCTTTA | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235841080 | CTCTGTCTATTAGGC[-/CAGTGACTAACTTCTTTA]CAGTGACTACTGAGA | 1130 |
rs538872429 | snp | A/C | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804549 | ATCTGCTGAATAATT[A/C]CCGAGGGCAACTCGA | 1130 |
rs538874988 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235883160 | TCTCGGCTGGCACTG[A/G]AAAGTCTCAGAAACA | 1130 |
rs538884213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792409 | AACCTCCGCCTCCCA[A/G]GTTCAGGCGATTCTC | 1130 |
rs538892818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694040 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG | 1130 |
rs538949996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793294 | TAATCTCAGCGATAT[C/G]TCTGGTTAATCCAAA | 1130 |
rs538962592 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792383 | GCAGTTGCACAATCT[C/T]GGCTCACTGCAACCT | 1130 |
rs538965590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828838 | AATTTTATTTACAGA[A/G]AAGTCATACAAATAT | 1130 |
rs538977301 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235860769 | TACACCCATGAAACC[A/G]TCATCAAATCAAGAT | 1130 |
rs539011858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778333 | GTGTCTTCTCTCAGA[A/T]CTGGATGGGGGCCTT | 1130 |
rs539021858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762339 | GTAAGACAAAGTAGA[G/T]AAAAGGTACCCTGAG | 1130 |
rs539029901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866174 | TCCCAGCTTATTTAA[C/G]TCATCAGAAGCGAAG | 1130 |
rs539063168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829456 | TCATATTGGTGTTAC[A/G]AACACTTCATTATTT | 1130 |
rs539108058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716392 | TTACATAAATAACAC[G/T]AGGGGATACGAATAG | 1130 |
rs539111435 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235798600 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAA]CACTGAAAAAAGGAA | 1130 |
rs539126657 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235855780 | AGATATTTATAAGCT[C/T]TAAATACACCTTGCA | 1130 |
rs539140193 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235805319 | ATTGTCCCCACTTCT[A/T]AGAGCCACATCTATC | 1130 |
rs539146732 | snp | G/T | 0.00353766 | 0.0419084 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806228 | AACTCAACATGTAGA[G/T]CCAACGACACATAGA | 1130 |
rs539158336 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235724856 | CAAGAAAACAAGGGA[A/G]ATGACATCCCCAGAA | 1130 |
rs539160952 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235793920 | TCACTGCAACCTCCA[A/C]CTCCCAGGTTCAAGC | 1130 |
rs539170966 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235810901 | GTAATCCCAGCACTT[-/TG]GGAGACTGAGGCGGG | 1130 |
rs539188013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235748039 | TGTTTGAGGGCTGAA[C/T]AAACGGATAAAGAAA | 1130 |
rs539199379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755193 | AGGAGTTTGAGACCA[A/G]CCTGGCCAACATGGT | 1130 |
rs539214694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235694486 | CTTGCAATGTTTTAA[G/T]TTCCTAAAGGAGAGA | 1130 |
rs539216723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850677 | AAACTCAAACAAATC[A/G]GTAGGAAAAAAACAA | 1130 |
rs539218834 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718852 | TCTAATGGGACCAAT[G/T]AATTTTGTTTCACTG | 1130 |
rs539229577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842731 | TCCTTTACCTTCTGG[A/G]AATGAAATGGTCACT | 1130 |
rs539253661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235833890 | AATAATAGCTCTCTA[C/T]TTTTCCTCTTCCAGT | 1130 |
rs539259125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678553 | AACTATTATCATAAA[A/G]CATTTCAATATTTCC | 1130 |
rs539260339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235800563 | CATTTTCTTTTTATA[C/T]TGATTGATTTTTCAA | 1130 |
rs539264860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843918 | TTAAAGTAACACTAC[A/G]TGCTTGCCTAATTTT | 1130 |
rs539267059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700173 | TTCAGGACATAGGCA[C/T]GGGCAAAGATTTCAT | 1130 |
rs539274789 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235756233 | TCACAGTAGTGATAG[A/G]CTCCTTTCCCCCAGA | 1130 |
rs539285405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783103 | AACTCCATTTTAAGA[C/T]AATGAGAGTAATCTA | 1130 |
rs539306656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835457 | CTGGTCAGCTAGATC[C/T]GTCTGTTTCTCTTAT | 1130 |
rs539309883 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672856 | TACTGACCTCCCAAC[A/G]TTTGAGACAAAGGAT | 1130 |
rs539321564 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675259 | ACTTGTTCTATAAAC[C/T]ACCCTTCCTGCCTTA | 1130 |
rs539344501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836172 | AAACACTGATTTAAT[A/G]TATTAGCTACCTCTC | 1130 |
rs539395551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872902 | GCCTGGGTGACAGAG[G/T]GAGACTCTGTCTCAA | 1130 |
rs539408695 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235745432 | AACAACAAACACTAG[A/G]TAAGGATGTAAAAAA | 1130 |
rs539414922 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235873445 | AACACTAGACAAATA[C/T]ACAATATACAACGTA | 1130 |
rs539425274 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235745337 | ATATATATTCATTAG[C/T]CAATATGGAAATGCA | 1130 |
rs539440366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848496 | CAAAGCAAACCCAAA[C/T]CCAGCAGAAGAAAGG | 1130 |
rs539461517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714760 | GAAGTTGCCGGTGTG[C/T]GTCTTTTATTAACTA | 1130 |
rs539473923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858327 | AAACATAAGCATGAT[A/T]ACCTATGGAAAATAT | 1130 |
rs539478505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698472 | TCAGGAATGCTCATG[G/T]GGGAACAGAGACGTT | 1130 |
rs539489723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813152 | TGAACCAAAAAATCC[C/T]TTTTCTTGAAAGTCT | 1130 |
rs539508675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699693 | AATTTACATTCCCAC[C/T]AACGGTGTAAAAGCG | 1130 |
rs539543802 | snp | A/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806683 | AGAGTTTCAAATGCT[A/T]TTAGAGAATGACTTC | 1130 |
rs539553084 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820472 | CTGCCCAGGCTCAGG[C/T]GATCCTCCCGCCCCA | 1130 |
rs539584315 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235883047 | GGCCAGCTCCTGGAG[A/G]CAACAGCACTGCCAG | 1130 |
rs539601035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235774375 | AAGGGTAGAGCAATC[A/G]TCTTTTGCCTTAGTA | 1130 |
rs539641666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679895 | TTTCAGGATTGATAG[C/T]GTCCTCAGGGCTAAA | 1130 |
rs539653810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686719 | GCCTAAATACAAAAC[A/T]GATCTAACTCAAAAT | 1130 |
rs539665440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864547 | TTAGGGCAACAGTTC[C/T]GGATTGGTATCCCAG | 1130 |
rs539667604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670089 | GCTTAATTTGTAATT[A/G]GCAAACCTCTATATG | 1130 |
rs539674280 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235708589 | AATTTCAGTATGTGC[A/G]AGGCAGAGGGTGCCT | 1130 |
rs539687460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235712314 | AATGCTAATTTTGTT[C/T]GCCCATAGTTTAAAA | 1130 |
rs539693750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235819237 | ACAATTCATCATTGG[A/G]GAAGTTCTCTTCAAT | 1130 |
rs539698130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723015 | AAACCAGGATGGTAG[C/G]AGTGGAAGCAGTCAG | 1130 |
rs539729355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811237 | TCAACATAAGAGATG[C/G]TGTAGATTATCTGGT | 1130 |
rs539750672 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235704455 | TAACCATTCTGACTG[A/G]TGGGAGACGGCATCT | 1130 |
rs539755894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812343 | ATCCCATCTGTATGT[A/C]CTAAAATGCAAAAAT | 1130 |
rs539766750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804872 | GATAAAATACTTAGT[C/T]CATCTTATTTGGTTT | 1130 |
rs539767804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865327 | CCTCCCTCTTCCCTG[C/T]CCTCCCTCTTCCGTG | 1130 |
rs539826028 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235764970 | TACTGATTCTTCATT[C/G]TTGTCCTACCCTCCA | 1130 |
rs539846757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669137 | CCCTTGGAATTTACT[A/G]TCTTCTGTATGCTAA | 1130 |
rs539854433 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703673 | TATAAATGCCAAAAT[A/G]AAATTCCAAAGATAT | 1130 |
rs539882963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798151 | ACTGTCAAGGCTAAC[A/G]AAAACAAGGAAAGTC | 1130 |
rs539884570 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802508 | AGTGTTTGTCTGCCT[A/G]GCTTGTTTTCATTTA | 1130 |
rs539891445 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869074 | CGATACTAAATATAC[A/G]TATCAAATAAAACTT | 1130 |
rs539915079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235817752 | GGATCAAAAAACTAT[C/T]GATTGGGTACCATGC | 1130 |
rs539915325 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701500 | GGGTGTGGTGGCGGG[C/T]GCCTGTAATCCCAGC | 1130 |
rs539918699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235711353 | GTGGCATGAATCTAC[C/T]GATGATTCAATAATC | 1130 |
rs539940871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790403 | TGTTAAGATTAAAAA[A/T]GTATATAGAACCAGC | 1130 |
rs539954987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710573 | AGGAAATGATATGAT[A/T]TACGCTGTAAAAAAC | 1130 |
rs540013966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235760105 | AACTCAATTTACCTC[A/G]GGCTAGCAGTTACCA | 1130 |
rs540016270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235768016 | CCCCTTTTTCTGGTT[C/T]CACATCCTGAAAATG | 1130 |
rs540023021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682850 | TTTTAAACAGAACAA[C/T]TATCTCCAATTCACT | 1130 |
rs540064535 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235822567 | ACCATGAGATCATCA[A/G]TTCAACCCTGAGGTC | 1130 |
rs540072477 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810389 | TTTACGCTGTCGTCT[A/G]CTTTTTCGAAAAACA | 1130 |
rs540075522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235838109 | AGTATATTTGGCAAT[A/G]GGAGGACCAAGAATT | 1130 |
rs540078908 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732657 | TTGTTAACATAAAAA[G/T]TAAAATGTGGTATCT | 1130 |
rs540109540 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235683633 | TCCTAAGATCCCCTT[C/G]AAAGTATTTTCAAAC | 1130 |
rs540124842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780147 | CATGGTGGCTCATGC[A/C]TGTAATCTCACCATT | 1130 |
rs540126494 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235876723 | ACTTGTAAAAATGAC[A/G]TAATCATTTGCCCAG | 1130 |
rs540140648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804391 | ACTGAACTCATCTGA[A/C]CAAGTCCTAGTCCAT | 1130 |
rs540141761 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736383 | AAGGTATAGAGTGAT[C/G]TGGGTCATGGCCAAA | 1130 |
rs540145532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235727025 | AATGAGAAAAGAATG[C/T]TGTTCATATTTCTGA | 1130 |
rs540176917 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844067 | ACAGAATAATAAGTG[C/T]CCAATAAATTCTGTT | 1130 |
rs540179555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729723 | AGAGAGGATATGCTT[C/T]ATTTTACCTAGTAAA | 1130 |
rs540184720 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671806 | AATGGGAAGCAATTA[C/G]ATTAAGAAGAGGATG | 1130 |
rs540187588 | in-del | -/AATT | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235689082 | TTTCTCAAATCAAAG[-/AATT]AATGGGTGAACAAAA | 1130 |
rs540187703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235801858 | TCACTAGATGAGAGC[A/G]AGAAAACTGACTGTG | 1130 |
rs540230159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668689 | CTCAGGATCAGTCCT[A/G]ACTTTCAAACACTGC | 1130 |
rs540230556 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235686132 | AGCACTTTGGGAGGC[C/T]GAGGTGGGAGGATCA | 1130 |
rs540230931 | snp | A/G | 5.01853e-05 | 0.005009 | intron-variant | LYST | GRCh38.p7 | 1:235724204 | AAGAAATAGGCAAAA[A/G]TATTTGTTTTACCGG | 1130 |
rs540242069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870127 | AAACAATAGTATTAA[A/G]AAACATGTATGTTCT | 1130 |
rs540257254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773617 | AAGTAGAATGGTGGT[G/T]TCCAGGGGCTAGAGA | 1130 |
rs540275177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758897 | TGGCATAATGAAGAC[A/G]TTTCCAGAGGGGTAG | 1130 |
rs540290126 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235720002 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 1130 |
rs540296216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235689844 | ATAAGAATTTTAAAC[A/G]ACTTTATTCAAGCTT | 1130 |
rs540311808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803271 | ACCTCAAAAAGGGGG[G/T]TTCTAACAAAGTAAG | 1130 |
rs540314603 | in-del | -/AT | 0.0646451 | 0.170115 | intron-variant | LYST | GRCh38.p7 | 1:235668203 | TATACATACATAGAC[-/AT]ATATATATATATATT | 1130 |
rs540315117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808410 | AAAAAGATCTAGACA[C/T]GCTCAACAACCCCCG | 1130 |
rs540335501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695971 | AGGTAAATAATTCAC[A/G]CATGTTGGTACTTTG | 1130 |
rs540344905 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235794451 | TAGAATTCTTTGGAG[C/T]AAAATAATAACTAAT | 1130 |
rs540344915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235802371 | GCAATATAGTTCCAT[C/T]CTAAAGACAAATTGA | 1130 |
rs540378345 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235855587 | TTCCATACCTCCTGA[A/G]GAATGCTAAAAACAG | 1130 |
rs540394798 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235833458 | CAAACTATACATCCA[A/T]CTCTACTAAGAAAAG | 1130 |
rs540396684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875164 | TTTGAAGATCTTTTC[C/T]AAAGTGAAAGAGTCA | 1130 |
rs540402066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235734832 | GATTATGCACTGAGT[A/G]TTTGATGACAGAGGA | 1130 |
rs540415048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235763490 | CAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTAT | 1130 |
rs540422721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724999 | AAACAAATTGACGTA[A/G]GTTCACAGCAACTTG | 1130 |
rs540424584 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235694178 | CCATGCCCGGCTGAT[G/T]TTTTTTTTGTATTTT | 1130 |
rs540443314 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867233 | GGCTCTGCGTAGTGG[G/T]CTGCGTCAGACCCTG | 1130 |
rs540473426 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235731580 | TTTTTTTTTTTTGAG[A/G]CAGAGTCTGGCTGTG | 1130 |
rs540478842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764083 | GCAACACCACTTTCT[C/T]CTAGTTCCCTGTCAA | 1130 |
rs540491728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675679 | TGTGCCTCTTCAGCC[A/G]CTGTTCATTTCTATC | 1130 |
rs540502859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773083 | GCATCTTGGGAAGCC[A/G]AGGCAGGCAGATCAC | 1130 |
rs540518334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717925 | CTGGAGTGAAGTGGC[A/G]TGATCTCAGCTCACT | 1130 |
rs540522308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779649 | TCCCTAAAGGATGTT[C/T]TCTTAATGGTGGGAC | 1130 |
rs540546112 | in-del | -/TTAGCATTCTATTAG | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235729821 | AATATTAGCTCCTTT[-/TTAGCATTCTATTAG]AAGAGAAATGACTGA | 1130 |
rs540560051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735758 | ATGCTGAATCACATC[A/G]TGTCATTTCCCAAAA | 1130 |
rs540597251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749153 | ATGGACTTGAATTAG[C/T]TTTTGTAACCACACT | 1130 |
rs540604426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667666 | CACATCCTCCTGTAT[C/T]CTTTTTTTTTTTTCT | 1130 |
rs540616740 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | LYST | GRCh38.p7 | 1:235752350 | ATATGTAGTATGTAT[A/G]CTAGAAATAGAAATA | 1130 |
rs540633991 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235721597 | CTTCAGACACAGGAA[G/T]AAGAGCCACAGATAT | 1130 |
rs540634120 | snp | C/T | 9.92457e-05 | 0.00704365 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757322 | GTGATGGGTGGTTAA[C/T]GAGGACCAAAAGTGT | 1130 |
rs540634209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732233 | ATTTAACCATATTAC[A/G]GTTTATAACTTGTTT | 1130 |
rs540649033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852471 | TCTCAGCACTTTGCC[A/G]GACCTTTTTCCCGGG | 1130 |
rs540669027 | in-del | -/GAA | | | intron-variant | LYST | GRCh38.p7 | 1:235841631 | AGAGAACGAATGAAT[-/GAA]GGACAAAATTCATGG | 1130 |
rs540721744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882255 | AGGGAATAGCATAGG[A/G]AGTAAGGAGGCAATT | 1130 |
rs540724712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695448 | CCAAATACATTGTGC[A/G]AAGAAATTAAGTGTA | 1130 |
rs540745866 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687438 | GCTTTTATTTTCCTC[A/G]TTTTATGTCTTTGGT | 1130 |
rs540779294 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741424 | CTGAGATACTTACTT[C/G]TAGGGATGGGCTGAG | 1130 |
rs540826585 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235822100 | AAAAATACTAACAGC[G/T]TGGCCTAAAAGGGAT | 1130 |
rs540828980 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867957 | TCCCAAGCCTATATA[A/C]CAAATGTTACTCCCA | 1130 |
rs540846032 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793715 | TTGTCACTTTTTGAA[C/T]GGATTATAAAAAATC | 1130 |
rs540865094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707186 | ATCTACCTTGGAGAG[A/G]AAAGTTGGCTTTCCT | 1130 |
rs540865489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822734 | GAGTCTATTTCCCCA[A/T]CCCTTAAATCTGAGC | 1130 |
rs540892647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815051 | TAGTTCCTCTGTGGG[A/G]AGACTTCTCTAACAC | 1130 |
rs540931326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807615 | AATGCCACACACGAA[A/G]ATATTGATAGGTTAT | 1130 |
rs540963944 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235859656 | AGTAATTATCTGCAT[A/C]CCCATTCACCCTCAG | 1130 |
rs540971129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850865 | GCCATAATCAAAAAA[C/T]CAAAAAACAGTAGAT | 1130 |
rs540980625 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235799176 | CCTTACAGTACAATC[G/T]CAGTTAATAAATGAA | 1130 |
rs540990190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856727 | TAAATAAGGCTAATA[A/G]AGAAATATTTCAAGA | 1130 |
rs541012698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680900 | CACCGCGCCTGGCCT[A/G]CAAGTGATTTTCATA | 1130 |
rs541016633 | snp | A/C | 4.97071e-05 | 0.00498509 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744042 | AAATGGATTGAAAAC[A/C]GAAGACTGTTCATGA | 1130 |
rs541054569 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235771594 | ATATTTTAATCTATC[-/T]TATCTTTTTTTTTTA | 1130 |
rs541069550 | snp | C/T | 1.66333e-05 | 0.00288381 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793520 | TACAAGGAGATTTCT[C/T]CAGAAATATTCTCAA | 1130 |
rs541073048 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865635 | GACAGCAAAGAGCTA[A/T]CAGAAAAAGAGTTGT | 1130 |
rs541092139 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680818 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 1130 |
rs541100511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681619 | CTGGGGCAATGGTCA[C/G]GGGGACATCTGGAGG | 1130 |
rs541108063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714883 | TATTAGGTAGAATGT[C/T]TTTAAAAAGTGAACT | 1130 |
rs541111176 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235724403 | ACTAGTTTTAGGTTT[A/T]CAGAAAATTGAGCAG | 1130 |
rs541118007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762024 | ATATGCCTAATGCTA[A/T]ATGACGAGTTAATGG | 1130 |
rs541134194 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235681666 | TTTCTATTTATCCTG[A/C]CAAGAATTGCTGTGA | 1130 |
rs541146662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714370 | CAGGCCAACAATTTT[C/T]AAATATTTGAACAGC | 1130 |
rs541155652 | in-del | -/TTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235856959 | TTTTTTTTTTTTTTT[-/TTTT]GAGATGAAATCTCAC | 1130 |
rs541176869 | snp | C/G | 0.000131935 | 0.00812096 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806017 | CTTTTTATAGCCAAA[C/G]ATAATAAATCTTCCT | 1130 |
rs541197064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235754581 | TGCCAAATCTTAGCT[A/G]TCACTTTCATCTGAT | 1130 |
rs541207027 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235755338 | AAGTTGCAGTGAGCC[A/G]AGATTGCACCATTGC | 1130 |
rs541212059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686341 | CATTGCATTCCAGCT[C/T]AGGCAAGAGAGGGAG | 1130 |
rs541244843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762627 | TTGAATGAGGTTGTA[C/G]TACATATACTTCTAA | 1130 |
rs541247881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235841166 | CTCAAAATGTATACC[C/T]TCTCAACAACTATCC | 1130 |
rs541253191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235692996 | TTTGCACTCCAGCCT[A/G]GGCAACAGAGCGACA | 1130 |
rs541259074 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235788607 | TTTTTGTTTTGCTAT[A/G]ATGAACTTTTATTAG | 1130 |
rs541265858 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235829848 | TAGCAGCCTCCAAAA[A/G]TTTTTCAAAAACATA | 1130 |
rs541267049 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806399 | CCCTGTCAGACTCTG[C/T]TTCTTTACTTACGCA | 1130 |
rs541285017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833307 | AGAAACAAAGAATAT[A/G]TAACATGAGGTTATA | 1130 |
rs541288090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826808 | CACCTCAGCCTCCTG[A/C]GTAGCTGGGACTATA | 1130 |
rs541300604 | snp | C/T | 3.31923e-05 | 0.0040737 | intron-variant | LYST | GRCh38.p7 | 1:235687073 | GGACCAATCAAAGAT[C/T]ATCATGTTTTAAAAG | 1130 |
rs541312065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235800657 | TGAGGATTTACTACT[A/G]GCTAGCAAAGGACAT | 1130 |
rs541320546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699922 | AGAACAGAGACTTAA[C/G]AAATAACACCACACA | 1130 |
rs541337856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235679483 | TGCTTTAAATGATAT[G/T]TATTTTATTATAACT | 1130 |
rs541352966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799869 | GATCTGAGGAACAAA[C/T]GAGATAATGCATATA | 1130 |
rs541413343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672531 | ATACCTAGAAAAAAG[C/T]AACTTTGGCTGCTTT | 1130 |
rs541427247 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235680257 | ATCATAGTTTTGTTT[A/T]TTTGTTTTTGTTTTT | 1130 |
rs541428219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769415 | GTTGTCACAGATTTT[G/T]AATTTTAGCCCAACT | 1130 |
rs541465408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776329 | CTTATTGCAAAATTA[A/G]TCAACGATGCTTCCA | 1130 |
rs541485257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235760370 | TAGCCTAAACAGCCC[C/T]AGACAGTTCTCTCTC | 1130 |
rs541486324 | in-del | -/A | 0.483852 | 0.0883933 | intron-variant | LYST | GRCh38.p7 | 1:235736847 | TTGTATCTTCAACAG[-/A]AAAAAAAAAGTCAGT | 1130 |
rs541497933 | snp | A/C | 6.62241e-05 | 0.00575392 | intron-variant | LYST | GRCh38.p7 | 1:235770134 | TGTGGAATATATTTC[A/C]AAAAGTAAAGTTACA | 1130 |
rs541499258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704833 | GCCAATTGCAATGGC[C/T]ACTTAATGTACTCAA | 1130 |
rs541500143 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235724920 | TAAGCAGGGAGTGAT[A/C]CTCTGGTTGCTCTGT | 1130 |
rs541504627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798343 | TCATTAATTATAATA[C/T]ATATATCATAAAAAA | 1130 |
rs541507322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873065 | AGGAGAAAGGAGGGT[A/G]AGAGAAGGTGAAACA | 1130 |
rs541543113 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768892 | TATTCCCTACAACAA[C/T]AGTCTAATTTACCAC | 1130 |
rs541562916 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235698059 | ACATGATGCCCTTTT[A/C]AAGAGTTTCCCCAAA | 1130 |
rs541573469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665182 | TATGTGTACAGTAAC[A/G]AGGTAAAATAATCAT | 1130 |
rs541592315 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235877568 | TGCACCACCACATCC[A/G]GCTAATTTTGTATTT | 1130 |
rs541602484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669805 | TTCTTTTGTTGCTTC[A/G]TGCTTTCTTTGCTTT | 1130 |
rs541603949 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235709691 | AATCAAACTAAGGCT[C/T]TGTAGAAGCATTTCT | 1130 |
rs541604114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738180 | GACAAATTGAAGGGC[A/G]AGATGATGGATCTCC | 1130 |
rs541622975 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774922 | ACATACCTTCAAAAT[A/G]TAAAACCCAACAATG | 1130 |
rs541632203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841943 | AAATGGGGGAAAGTA[A/G]TGATGACAGACAAAA | 1130 |
rs541636143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687432 | CTTTTTGCTTTTATT[A/T]TCCTCGTTTTATGTC | 1130 |
rs541646500 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235745531 | TCTTAAAAAACTACA[C/G]ATGTAATTACCGTAT | 1130 |
rs541681298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767626 | ATCAATAGTCACTGG[C/T]ATTCTATTTTATTAT | 1130 |
rs541686897 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700702 | AAGCAGTGGCATAAA[C/T]GTCATTACACATCAC | 1130 |
rs541697250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677337 | TTCAATAAAATATAA[C/T]AGGTAATCTTACTAC | 1130 |
rs541706995 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235705746 | ATGGTTCAGGATTAT[-/A]AACAAAAAGGGTATA | 1130 |
rs541710898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775729 | AAAGCAGGAATAAAG[A/G]GGTGGCTAAGGCAGG | 1130 |
rs541735356 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884420 | AGCCACCGCGCCCGG[C/T]GCCCAGCTAATTTTT | 1130 |
rs541743557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879925 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 1130 |
rs541752314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871077 | GAAGTGCTTTACCTT[A/G]TTAGGATGCATATAC | 1130 |
rs541766636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235810600 | TCAATTTTAAGGTGA[C/T]AGCCCTCTTATTTAT | 1130 |
rs541778761 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235880582 | ACTGCCTAGATGGAA[G/T]GTATACATACCATGT | 1130 |
rs541787602 | snp | A/G | 1.70478e-05 | 0.00291952 | intron-variant | LYST | GRCh38.p7 | 1:235743943 | CTCTATTTCCTTTGT[A/G]TGAATGAACATTTCC | 1130 |
rs541789105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863946 | AGTCTGTTTAGCATA[A/G]CATCCTGGATATCTA | 1130 |
rs541794235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761160 | TTAAAATATTATTAT[A/G]AAAGAGCATAAAAAG | 1130 |
rs541811824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860313 | CCCCCCTAAACTGGT[A/G]CATTTGTTATAATCA | 1130 |
rs541830853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751517 | ATTTTTAAATTCTTG[C/T]TAAAAGCAATTTTAA | 1130 |
rs541852346 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235848200 | CTCAGACCACAGCGG[A/C]ATAAAACTGGAAATC | 1130 |
rs541854349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856220 | GGTAAAATAAGGAAA[C/T]TACATATTGAAAACC | 1130 |
rs541874134 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235698351 | TCTTTTAAAAAAATC[A/G]TGCCACTTTAGGAGC | 1130 |
rs541883110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235839141 | CATTTTCGTTCTCTA[C/T]ATATAAAATGTAAAA | 1130 |
rs541888829 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235782399 | AGGATGGTCTCTATC[G/T]CCTGACCTCATGATC | 1130 |
rs541900373 | snp | A/C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235792401 | CTCACTGCAACCTCC[A/C/G]CCTCCCAGGTTCAGG | 1130 |
rs541910999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705442 | CCAGGCTGGAATGCA[A/G]TGGCACGATCATGGC | 1130 |
rs541933086 | in-del | -/GCCC | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235863112 | AAAATCTTGAACTTG[-/GCCC]AGCACGGTGGCTCAC | 1130 |
rs541955908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753399 | AGTTGGGGGAGTAAG[A/G]ATTCTTAACCTGTTT | 1130 |
rs541963974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729038 | CAGGGTTCTCACACT[G/T]GGAGAACCTAGCCTA | 1130 |
rs541966843 | snp | G/T | 0.00036601 | 0.013523 | intron-variant | LYST | GRCh38.p7 | 1:235788682 | TATCTATTCATGGGA[G/T]GCTGAGGATAATCAA | 1130 |
rs541975263 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823973 | GTACTTAATGGTCTG[C/T]TGAGTAAAGCAGTGA | 1130 |
rs541982634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678101 | AAAAGGTTTTTAGTA[G/T]ATTAGAGGGCAGACC | 1130 |
rs541985636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235691750 | TGCTGATGCTGGAGC[A/G]CAATGGCACGATCTC | 1130 |
rs541987536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736895 | AAAAAATAAGAGGAG[C/T]GGAAAGGGATAAAAG | 1130 |
rs541990146 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235861938 | ACAAAACAATTAGGC[C/T]AATCCCTGCATATTA | 1130 |
rs542001330 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235720013 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT | 1130 |
rs542034376 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235767875 | TTCTCTGAACTTTCT[A/T]TATCATTTGGTTCAA | 1130 |
rs542042839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758815 | TAAAATAAGGAAAAA[C/T]ATATCTTTCTGTTTG | 1130 |
rs542070333 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669909 | GTGACACTGGGAGCA[G/T]AGTGGGGGGTGGGGA | 1130 |
rs542072417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670208 | ACCATATGTAGAAAA[A/G]TTTAAGTCTTAGCCA | 1130 |
rs542078847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825467 | CAGAAAAGTTTCAAG[A/G]TCTAATGAATGAATT | 1130 |
rs542097967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710498 | GGTGTTCTGAGGGAA[A/C]ATCTGACTCCTGACC | 1130 |
rs542102013 | snp | A/G | 9.89936e-05 | 0.0070347 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809182 | CAATGCAACAGCACC[A/G]CTCAGGATAATAAAC | 1130 |
rs542122365 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235710502 | TTCTGAGGGAACATC[G/T]GACTCCTGACCCAAA | 1130 |
rs542122847 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235755201 | GAGACCAGCCTGGCC[A/C]ACATGGTGAAACCCC | 1130 |
rs542158520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235711899 | TAAAATCCTCAAGCT[C/T]ATTTGAAAATAGAAT | 1130 |
rs542169564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726173 | TCTTCTGTGTTGACT[A/C]ACAGGAAGCTCAGAG | 1130 |
rs542194796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684017 | ACCTAATACTTAGGT[A/G]GAAAAAAAATCCTAT | 1130 |
rs542209198 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661395 | GCAATTTTTTGTTAA[C/T]AAAGCAAATCACTTC | 1130 |
rs542268802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691182 | CTCGGCCTCCCAAAG[C/T]GCTGGGATAACAGGC | 1130 |
rs542273894 | in-del | -/TCT | | | intron-variant | LYST | GRCh38.p7 | 1:235694001 | GAGGCTCTGTTCTTC[-/TCT]TCTTCTTCTTTTTTT | 1130 |
rs542287326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823941 | CCGCATCTAGCAGAG[A/G]TGCTGGGCCATAGTA | 1130 |
rs542299383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831299 | CTTGCCAAGAGGCAC[A/T]GTCAAGCTCTGGGCC | 1130 |
rs542305016 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832525 | ATGTTTATATGAATA[G/T]GTTAGTGTATATACA | 1130 |
rs542324349 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235862331 | TCCAAGGTTTCAGTT[A/G]CCTGAGGTCAACTGT | 1130 |
rs542329218 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235880362 | TGCATGGTAAGAATG[A/G]AGGTTGTAAGATGTA | 1130 |
rs542349770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877072 | CTATGTCCAGTCCTG[G/T]ACAAAAGCATCTGAG | 1130 |
rs542394470 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235811018 | GATGTGGTGGTGCAC[A/G]CCTGTAATCCCAGCT | 1130 |
rs542413268 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714979 | TGCATTTTTATAAAC[-/TT]AGACATTTAATTTGA | 1130 |
rs542416505 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693682 | GTTCTCAGGGTGGGA[C/T]TATATTTTTTCACTT | 1130 |
rs542430088 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661137 | TGCTACAACATGCAC[A/G]TTATGAAGTATTTCA | 1130 |
rs542463282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235695376 | TGCCTGTGGAGGCCA[C/T]GGAGGAAACTGTTCT | 1130 |
rs542487679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690537 | ATCTTATTAAAGTTC[C/T]TAGTAAAGTTGTTTT | 1130 |
rs542489303 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235844260 | AAAAATAAAAAATCT[-/TTA]TGAGAAAAAAAGATA | 1130 |
rs542505499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696956 | CATTCCTACTTTGCA[C/T]TAAATAACCACAAAT | 1130 |
rs542506386 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235725312 | GATGGCAGGCACCTG[C/T]AGTTCCAGCTACTCG | 1130 |
rs542522113 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235803749 | TTTTACAGTTAGTCA[A/C]TTAATTCAGTAATAT | 1130 |
rs542522382 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235773096 | CCGAGGCAGGCAGAT[C/G]ACTTGAGCTCAGGAG | 1130 |
rs542524655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689747 | TGTATATATACATGT[A/T]TTAAAACATCACATT | 1130 |
rs542529515 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | LYST | GRCh38.p7 | 1:235786662 | CCCAAATGTCCATCA[A/G]TGATAGACTGGATTA | 1130 |
rs542542176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235839071 | CTCAAGTGAACCTCC[C/T]GCCTTGACTTCCCAA | 1130 |
rs542555539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846264 | GTGGCTAGACCCAGA[A/G]GAGAGACAACAATCA | 1130 |
rs542564822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794981 | TCCGTAACAGCAAAA[A/G]TATGTGGGGGCAGTG | 1130 |
rs542585236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235741922 | ACAATGGAATATTAT[C/T]CATCCTTAAAGAGGA | 1130 |
rs542608793 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756909 | AAATTTGATAGTACA[C/T]TGAAGAAGAGATTTC | 1130 |
rs542617221 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235666650 | CATGCCCAATGTTCT[A/T]CTAAGTTTTCCCATT | 1130 |
rs542621949 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867786 | ACTGGGAAAAAGCCT[C/G]AACTGTAATCGTTCG | 1130 |
rs542641991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823626 | AATCCCCGTTTTACC[A/G]AAAGCAAAGCAAAGT | 1130 |
rs542665342 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235851167 | AAACTGTGGTATGTA[A/T]GTATGTATGTATATG | 1130 |
rs542672088 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235752936 | TCAGAGGTACACAGA[A/G]AGGCTTCTTACATAG | 1130 |
rs542676638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815882 | TCACGCCTGTAATCC[C/T]AACACTTTGGGAGGC | 1130 |
rs542677660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779524 | TCTTAAAAATGTAAA[C/T]TCCAGGGTCACACTT | 1130 |
rs542691472 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735465 | TTAAGATAATGACAA[C/T]TGGCCTTTGCAGCAC | 1130 |
rs542692822 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235807556 | AAGGCATTGATTTAA[A/C]ATCAATAATAGTTTT | 1130 |
rs542697942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235814973 | TTCCTCACATACACT[A/G]TTTCTGCAATTCTCC | 1130 |
rs542706364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773592 | TATATGAGATCCTTA[G/T]ATTAGTCAAAAGTAG | 1130 |
rs542774745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235741191 | CTGACAGAAACTCTG[A/G]AACAGAACTTCTTAA | 1130 |
rs542777301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708735 | TTGTGCTTTACCAGG[A/G]GTAGATTCTTGGATG | 1130 |
rs542784816 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859433 | TACCAAAAGTATTTG[A/G]AAGAATATATTTACT | 1130 |
rs542788757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673511 | GTTAGACATCCTCAG[A/C]TGATTGCACCACCCT | 1130 |
rs542793553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845015 | GATTGCAGCTCTGGA[C/T]AGAGCAGCATGTGGT | 1130 |
rs542800394 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235787118 | TAGAAGTTTCTGTAT[-/TC]TGTTTCAGAAGCTAT | 1130 |
rs542807093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235777857 | AAAGGATAGTTTCCA[C/T]CAGTGTGTGGCTCCC | 1130 |
rs542808180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873283 | CTCAGGCTGAACGTG[A/T]CATAGTGTTCTACTT | 1130 |
rs542808341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235732722 | TATTGAATATTTTCC[C/T]GTGTGTTTGGTAATT | 1130 |
rs542833213 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235729269 | ATATCTGATAAAATA[A/G]TAGGTAAGATATCAA | 1130 |
rs542845867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785076 | CTATTATTGAGGCTG[A/G]ACAGCTGTAAGCAAT | 1130 |
rs542850820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794357 | TAAATACTTAAATAC[C/T]ACAAACTATTTAGTT | 1130 |
rs542876505 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235666132 | CCACAGATCAAAATG[C/G]CCAGTGTGTTGCAGC | 1130 |
rs542885831 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235821125 | CTTGTATTGGTCCCA[C/T]GTAGAACTTCTTATT | 1130 |
rs542886319 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235725959 | AATCAAGAAAAACTT[-/A]AAAAAAATGCATCTT | 1130 |
rs542904523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764585 | CCTAACTGCAACCAC[C/T]GCTTCCCGGGTTCAA | 1130 |
rs542917840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785949 | ATACAGTACTCTCCC[A/T]GAATCTATCACTTGG | 1130 |
rs542930271 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235801984 | GTGGATCACGAAGTC[A/C]GGAGTTCGAGACTAG | 1130 |
rs542942103 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235719662 | TATATATAAAGCTCA[-/C]CATCACCACCTATAA | 1130 |
rs542961843 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883651 | TTGCGTTGCTTTTTC[A/G]TTTGGTAACGGGGCT | 1130 |
rs542984729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747314 | GAGGAATAATGGAAC[C/T]CTTCATTGGAATTGA | 1130 |
rs542997980 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235714509 | CATGAGTAAAAAGCA[C/T]GAAGTAGTTCAAGAA | 1130 |
rs543015204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235858694 | GCAGCCTCATTACCA[C/T]TCTCTATTCCTTGAC | 1130 |
rs543018847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738866 | CTTCCTTAGCATTCC[C/T]TGCATCTTGGGAGAG | 1130 |
rs543021537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755299 | GAGGTTGAGGCAGGA[G/T]AATCGCTTGAACCTG | 1130 |
rs543028271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763400 | GTAACCTGGAGCTAC[A/C]CTTGACCACTACCTT | 1130 |
rs543035275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842043 | CAGCTATTTCAGATT[C/T]ACCAGCAGGATTCAG | 1130 |
rs543051074 | in-del | -/AAG | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235665706 | CTTAATTCTTAAAAA[-/AAG]AAGAAAAAGTATTCT | 1130 |
rs543053889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235859251 | TTCCTCTCGTTACAT[C/T]TGATCAATTATCTTC | 1130 |
rs543057369 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676207 | CCATTTACTATTCTA[C/T]ACTATTGCTCTCTGT | 1130 |
rs543132044 | in-del | -/AGTGCATGGGATACA | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235760512 | AATTATTTTCATTGT[-/AGTGCATGGGATACA]AGTGCATGCCATTCA | 1130 |
rs543154960 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235840103 | CCAGCTATCATTTAC[A/G]AAACAACCACTTTGT | 1130 |
rs543154979 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235851834 | GGGAAAGATATGACA[A/C]TTAAAGTTCTAAATT | 1130 |
rs543162583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882058 | CACACACTCACACAT[A/C]CACACACACACTCTT | 1130 |
rs543167688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687406 | GTATGTGTACTTCAC[A/G]TATTTATTTGCTTTT | 1130 |
rs543170092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881472 | CAACAATTCCACTTC[C/T]GGTACATATCAAAGA | 1130 |
rs543187158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856602 | TGCATAATCAGGTTT[C/T]ATCAAAACTGCCTTA | 1130 |
rs543189989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748522 | TATAATGACCAGAAA[G/T]AGAAATCAATTTATA | 1130 |
rs543224011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235857477 | TCATTAACATATAGG[C/T]GGTATATGAAAGCTT | 1130 |
rs543239290 | snp | A/G | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826503 | TTTCAGAGACATGAG[A/G]GTACATACTACATGA | 1130 |
rs543240736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828278 | TAGGGGAATGGAAGG[G/T]ATAGGGGAACGATAG | 1130 |
rs543240888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835529 | GCTCTTAAACTGGCA[C/T]GGCTTCTTTATCTCT | 1130 |
rs543244497 | in-del | -/GCCTA | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235802504 | TGCCAGTGTTTGTCT[-/GCCTA]GCTTGTTTTCATTTA | 1130 |
rs543274069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761347 | CAATGTCCCAGTATG[C/G]AAAAGGACAGTAGTC | 1130 |
rs543277141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235821912 | ACTTAGGTGGTGCCT[A/C]GTACACCCTATCACC | 1130 |
rs543277782 | snp | C/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235829049 | TCTCTACTGAAAATA[C/G]AAAAATTCACTGGGT | 1130 |
rs543332564 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235681501 | TTAGGAAGGCCATCA[C/T]AGAGCCTACAAGGAG | 1130 |
rs543334974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866658 | CCCAGAAGCCAGAGA[A/G]GACGCCCCGAGCTGG | 1130 |
rs543335560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799220 | CAGAAAATCACTATT[C/T]GGCAGATACCACAGA | 1130 |
rs543356618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754303 | AATTGTGCAATCCTG[A/G]CTCACTGTAACCTCT | 1130 |
rs543359025 | snp | C/T | 0.000313084 | 0.0125078 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715243 | AAGGAGGCATCCTGA[C/T]CAGGAAGTGAAGCAC | 1130 |
rs543359133 | snp | A/G | 0.0010557 | 0.0229508 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724145 | TTCTTCATATGTCCA[A/G]GAAAATGATGCTGGT | 1130 |
rs543392430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850161 | CAAAATAGTGTGGTA[C/T]TGGTATAAAAATAGG | 1130 |
rs543401579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833260 | GATTGCACGGTATTT[C/T]CTTTAAATTTTTTCT | 1130 |
rs543412199 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235880395 | AGTAAGTTGATTGGT[C/T]AGTTATTCTAAGTCA | 1130 |
rs543457670 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235688201 | CACATGGATCCAGTG[A/C]ATCAACCTAAGTTAC | 1130 |
rs543465414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834437 | GAGATGGGGTCTTGC[G/T]GTGTTGCCCAGGCTA | 1130 |
rs543476621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877706 | CCACCGCGCCTGGCC[A/G]GTCAACTTTCTTTTT | 1130 |
rs543507497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235722485 | CTGAGCAAGTTTTTT[A/G]TTTTGTTTTGTTTTG | 1130 |
rs543508665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768490 | AAAGGCAAAGACTAA[G/T]TTCATTTCTTTATAA | 1130 |
rs543521708 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235874123 | CCTTGAAAAATGGTG[C/G]TACATAAAAAGATTC | 1130 |
rs543525209 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235715701 | AATGAGAGGTGCTTC[G/T]GTCACTAGAGATGTC | 1130 |
rs543534617 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235705463 | CGATCATGGCTCACT[A/G]CAGACTTGAACTCCT | 1130 |
rs543534633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739526 | TACATTACCATATTA[C/T]GTAAAGAGATCTACA | 1130 |
rs543543248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872021 | TAACATGGGGCCAAG[C/G]ACAGTGGTTCACACC | 1130 |
rs543544550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721779 | CTATAAGCCAAGCCC[C/T]GGAAGGAAAAGGAGG | 1130 |
rs543549748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713522 | TATGCATATATTAAA[C/T]CTGTGGTTCTCAACC | 1130 |
rs543554029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694079 | CCGTGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 1130 |
rs543563651 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235714313 | TCAAATTAACCAAGG[A/T]TAATTAGCCAGGGGA | 1130 |
rs543609755 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681075 | GGAGTGAGGGCTACC[A/G]AAGATGATTTTCACA | 1130 |
rs543622712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769281 | TGTACTCTGAGACAG[A/C]AAAAAGTCTTACTTG | 1130 |
rs543623695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840012 | ACCTACCTTTTCTTC[A/G]AATTTTAGGAACTCT | 1130 |
rs543647955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672357 | CCTAAGGTATGCCAT[C/T]GTTAAGAAGTAGACA | 1130 |
rs543656562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235698038 | TTTCAAAATGAAGAA[A/G]AAAAGACATGATGCC | 1130 |
rs543662381 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235832149 | AAAGTTTCAGAAAAC[A/C]ACCAGGAAAACATTT | 1130 |
rs543711695 | in-del | -/AG | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853966 | AGATATTGTAGCTAT[-/AG]AGAGAGAGAGACGGC | 1130 |
rs543770091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789703 | GATGACAATAGTTTT[A/G]AAAAAGAAGAGTTAA | 1130 |
rs543778262 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818580 | TTTCCATGTATAGCT[C/T]ATACTCAGTATACCT | 1130 |
rs543782657 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235815173 | CCCATTTTCCTCTTT[C/T]ATCCGTTAAACAAAT | 1130 |
rs543790946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825811 | CTAGTGTGCATTTTG[C/T]AGAAATAACAAGTTG | 1130 |
rs543806158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737645 | TGAAAAAGGCCATGT[C/T]GACACAACAACTTGA | 1130 |
rs543807891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669753 | CCACTTCCACACTGC[C/T]GAGTGTACTTTCATT | 1130 |
rs543822497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235711637 | TTGGTTATTAGATAA[C/T]TCTGGGCAGAGTATT | 1130 |
rs543833200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775645 | AGAGACCATTCTGAT[C/G]CCTCTCTGCTTGGTT | 1130 |
rs543840713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686292 | GAATTGATTGAGCCC[A/G]GGAGGCAGAGGTTGC | 1130 |
rs543843056 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235847058 | CTCAAAAAGATCTTC[A/G]CGTAGGCACATTGTC | 1130 |
rs543855714 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662213 | GTCAATATCTAGCGT[C/T]ACAGATTTTAAGTAA | 1130 |
rs543859627 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732066 | GTAGCGGTTGTTGTC[-/T]TTTTTTTTTAAAACG | 1130 |
rs543865068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827282 | GCTGAGACATGACAA[A/C]CTCTAGAACCCTGGA | 1130 |
rs543869147 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764877 | GACTCAGCTTTCTTG[A/T]AGGTACATTCTTGCT | 1130 |
rs543879617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235678395 | GGTGATGTTACCAAC[A/G]GTAATGGGCCCTAAT | 1130 |
rs543888398 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804416 | GTCCATATGCTCTAA[A/C/T]GACATTCATCAGCGT | 1130 |
rs543897752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776285 | AAATATTTGTAAGAA[C/T]CCTAACAACAACAAA | 1130 |
rs543905088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235671185 | TTAAGTGATCCACCT[A/G]CCTCAGCCTCCCAAA | 1130 |
rs543923765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803930 | CAACTAAAGGTAAAA[C/T]AAACATAAAATGAGA | 1130 |
rs544018977 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235866885 | GCACTCCCCCTCTCC[C/G]GGAGAACCCCGAGCC | 1130 |
rs544026563 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743131 | ATAAGGGGAAACTAC[C/T]CTATGGGTTTACCAT | 1130 |
rs544050791 | in-del | -/AA | 0.0501759 | 0.150234 | intron-variant | LYST | GRCh38.p7 | 1:235663083 | AAAATGTAAGGCTGT[-/AA]AAAAAAAAAAATTCC | 1130 |
rs544082091 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844464 | CACTGGACTCTACTA[A/T]CCCAGTTGTCTTGGA | 1130 |
rs544088557 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739737 | ATCACTATTTTGTAA[C/T]TCTTTAATGAAAAAG | 1130 |
rs544088639 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235779824 | ACAAAATACATTCCA[A/C]AACAGTAGTCTCCTT | 1130 |
rs544103052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782167 | AAGTATGAATATTTA[A/G]CAATGGGGAATTCTT | 1130 |
rs544105865 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235798301 | TGAATTATGGACTTC[A/C]GTTAATAATAACATA | 1130 |
rs544108744 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235741871 | TCTGAACGTCCATCA[A/G]TGGATGAACAGATAA | 1130 |
rs544119889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683751 | CTTTTAAAACCATGC[A/G]TTCAGTGGGTCAGGA | 1130 |
rs544136321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774332 | CAAATGTATGGATCT[C/T]GCAGTTTAAAGAAGT | 1130 |
rs544139042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745428 | TGACAACAACAAACA[C/T]TAGGTAAGGATGTAA | 1130 |
rs544143868 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235824375 | GTTGGCAATAGGGCA[C/T]AGAAGAAACCAGAAG | 1130 |
rs544149364 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235776334 | TGCAAAATTAATCAA[C/T]GATGCTTCCATTAAA | 1130 |
rs544180801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750693 | TTAATGTTTATTATT[G/T]GATGACATTCTTCCT | 1130 |
rs544183577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235817916 | CTATTCATTAAGAGT[C/T]TGAAGGAATCCACTG | 1130 |
rs544207810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854391 | TTCTATTCTCCAAAG[C/T]AGACATTGACTTCTC | 1130 |
rs544295701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846177 | TGGCTGAGAGACCCA[C/T]AGATGGTTCACATCA | 1130 |
rs544302313 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235777957 | AGACAGTGTCTTGCT[C/G]TGGCACCCAGGCTGG | 1130 |
rs544320044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712466 | AATTTTCGTCTATCT[A/G]TCAAAGTAGAATGAA | 1130 |
rs544322513 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662694 | TTTAATGTACCATGC[A/G]AGGCTTAAAACTTGT | 1130 |
rs544335604 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813758 | AGTTCAGAAAAAGGA[A/G]CAGTCATTATCAGAA | 1130 |
rs544342485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847431 | CAGAACCTCTTCAAA[C/G]CATAAATCACACAGG | 1130 |
rs544374788 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235868928 | TCGAACTCCTGACCT[C/G]AGGTGATCCACCCAC | 1130 |
rs544381160 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235803258 | CAGACAACTTAATAC[C/G]TCAAAAAGGGGGTTT | 1130 |
rs544390269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773699 | AAAAAGATTTACAGA[A/G]ATGGATGGTGGTGAT | 1130 |
rs544392368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764796 | GCGTGAGCCACCGTG[A/C]CTGGCCCCATTTACT | 1130 |
rs544392686 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235727263 | GAGTAGCTGGGATTA[C/T]AGGCGCCACCACCAC | 1130 |
rs544394700 | snp | A/C/T | 4.95073e-05 | 0.0049751 | synonymous-codon, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757419 | ACTTAGGAGTTCATA[A/C/T]AATCCACAGCATATA | 1130 |
rs544397981 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235724813 | CTTTTACTAAGCAAA[C/T]ATCCTTTTAAATACA | 1130 |
rs544402905 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235860327 | TACATTTGTTATAAT[C/T]AATGAACCTACACTG | 1130 |
rs544424279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235764233 | AGAAAACAAAAATGT[C/T]GACTGCCTTATCACT | 1130 |
rs544425588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824161 | TTTTTAAAAACCTAT[C/T]ATAATGTTTGAATTA | 1130 |
rs544441338 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235717658 | ACAGCAAGATTTGCC[C/T]ACATTTCAGTGAGTC | 1130 |
rs544448661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235831271 | AGAGGGCAGTGCACA[C/T]ATGACTATGCCTCTT | 1130 |
rs544449230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235823635 | TTTACCAAAAGCAAA[G/T]CAAAGTTCAGCCTTC | 1130 |
rs544459052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235758168 | GCTGCATTTCAGCTC[C/T]ATATAAAGTTATGGG | 1130 |
rs544494752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710658 | AATCTTGCTACTCTC[C/T]ATCACAAGGCAAAGT | 1130 |
rs544505937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235869802 | CAGAGCTCTAACACC[A/G]TCTGGCTCCTCAAAA | 1130 |
rs544508591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772773 | ACTCCCCTGACTCTT[A/G]GCAGTCTCCCCTTTC | 1130 |
rs544524893 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235836242 | TTCAACAAATGTTAT[C/T]GAACATTTACTGTAT | 1130 |
rs544527485 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235736528 | CAAGACACAAAGATA[C/T]GATTATCTTGAAAAG | 1130 |
rs544527602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719030 | CCTTTTCTATTTTTA[C/T]TTTTTGAGACGGAGT | 1130 |
rs544575551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724593 | TGTGTTGTACATTCC[A/G]TGGGTTTTGACAAAT | 1130 |
rs544593848 | snp | C/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235845634 | CTGGAAACAGACTCC[C/T]GGCAGTTAGGGGGGA | 1130 |
rs544596889 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235709903 | ATAGCAAAATTATCC[C/T]AACACAGGAAATAAG | 1130 |
rs544611737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235749817 | AGTTACGTAGGGCTC[C/T]AAGGCTCAAGGTGAC | 1130 |
rs544612756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235733069 | ATGGAATTTACTTTA[C/G]TGTCTAATGTTTAGT | 1130 |
rs544626222 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235785944 | AAATCATACAGTACT[A/C]TCCCTGAATCTATCA | 1130 |
rs544648314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683103 | GAGTAACAGTTATGG[A/G]TAAACACAACATAGG | 1130 |
rs544650456 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235728478 | TACATTACTAGCATA[C/T]AGATTTGCTTTATTT | 1130 |
rs544663093 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235696123 | AAACATAGATAAAAC[A/G]GTATGCATCCTCTCT | 1130 |
rs544680304 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235850578 | AAGTAACAGTCAGCA[C/G]AGTAAACAAACAACC | 1130 |
rs544687783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756223 | TCAATGACTCTCACA[A/G]TAGTGATAGACTCCT | 1130 |
rs544705598 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884549 | CACAATATGAGTTTG[A/T]AGCATGGATACTGCC | 1130 |
rs544710894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689681 | AAAAAATGCTAACTA[C/T]GTGAGGTGACGAATG | 1130 |
rs544736954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725157 | AAGGGGAATAGGCCG[A/G]GTGCGGTGGCTCATG | 1130 |
rs544775545 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235838376 | GGACTGTCAAATACT[C/G]CATGGGAATCTAGAT | 1130 |
rs544812509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876094 | CAGGCATGGTGGCAG[C/T]TCCTATAGTCCCAGC | 1130 |
rs544827904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235675475 | GATCGGTCGGTCGGA[C/T]GCAGGCAGCACCTTT | 1130 |
rs544851497 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235838097 | TGTAGGAAGATTAGT[A/G]TATTTGGCAATAGGA | 1130 |
rs544855524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835840 | CCCTCTAGGTCACAA[A/G]TTACTTAAGGCCAGG | 1130 |
rs544855597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844995 | GGCGAAGGGAGGCAG[A/G]ACTAGATTGCAGCTC | 1130 |
rs544874559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802539 | GTCCTCAATGTAAAC[A/G]TTGCCTCTTCAGAAA | 1130 |
rs544893368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235747644 | GTCTACATCTGACAG[C/T]TTTCATGCTGTACGT | 1130 |
rs544898695 | snp | C/T | 1.68599e-05 | 0.00290338 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808428 | TCAACAACCCCCGCC[C/T]CCGCCGCCACCCACA | 1130 |
rs544923771 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235802642 | TGGTATTTATTGTCT[C/T]TCACACTAGAATATA | 1130 |
rs544941584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701499 | TGGGTGTGGTGGCGG[C/G]CGCCTGTAATCCCAG | 1130 |
rs544942383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882916 | ATTGGAATCTCTCCA[A/G]TGAATGTCTTTGGCT | 1130 |
rs544982139 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235787723 | TCATAGAAAAATTAA[C/T]ATAAATGTCTAAGTA | 1130 |
rs545001075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682212 | GCTATTGGTAGGGGG[A/T]CGGGGATGGGGCTGA | 1130 |
rs545010661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673414 | ACCGCCCCCTTATCC[C/T]GCCTATGGTGGGGAG | 1130 |
rs545043011 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235783445 | TGAGAACATACGGAC[A/C]CAGGGAGGGGAACAT | 1130 |
rs545054457 | in-del | -/TTTTAT | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868699 | TACCAGTGTTTTTTA[-/TTTTAT]TTTATTTTCAAGATG | 1130 |
rs545056433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235822928 | AACAGCCCCACCCAA[C/T]AGCCCTCAGTTAATC | 1130 |
rs545057955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785888 | AGATATTCCACAAGA[G/T]GTTTCTTATTAACTT | 1130 |
rs545082517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235707849 | CATTTGGAACCAGAA[C/T]TGTTTTGGATTTCAG | 1130 |
rs545096761 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857297 | TGAATTGAGCCCTCA[A/G]CTAGATGGGCATGAG | 1130 |
rs545101743 | in-del | -/A | 0.143284 | 0.226079 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853493 | TGTGTAAAGAAAACT[-/A]AAAAAAAAAAACATG | 1130 |
rs545108510 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772625 | ATGTAGTGCCTACAT[C/T]TAAGATCAATCTATG | 1130 |
rs545117915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707218 | CTAACCCCCTTCACC[C/T]TATTTGAGTCTTATT | 1130 |
rs545128823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815272 | ATATCCATATCCTCA[G/T]GAAGCCTACTTCCTA | 1130 |
rs545149427 | snp | A/C | 1.6507e-05 | 0.00287284 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806424 | TACGCATAAAAAAGC[A/C]ACACAGAGGAATAGG | 1130 |
rs545159094 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684866 | ATTTCTGGGCTCAAG[C/T]GATCTTCTTGTCTTG | 1130 |
rs545166405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850932 | ACTGCTGGTAGGAAT[A/G]TAAACTAGTACAGCC | 1130 |
rs545192484 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235790801 | TAGCAATTCTTCAGT[-/TA]AAGAAGGAACTGGAA | 1130 |
rs545204343 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235760720 | AAATTTGAGACCATG[A/G]ACACAGAGTAAACAG | 1130 |
rs545209053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850340 | GTAGGAGAATGAAAC[C/T]GGATCCTCATCTCTC | 1130 |
rs545231541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235880778 | CTTCATCTTCAAAGA[C/T]TTTTCTTACGCAAAT | 1130 |
rs545236391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235783531 | CAAATACCTAATGCA[C/T]GTGGGGCTTAAAACC | 1130 |
rs545237836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235800752 | TTCACCTGAGGTACC[A/C]GAAAAGATAAGTAAT | 1130 |
rs545240869 | snp | A/T | 3.30087e-05 | 0.00406242 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808563 | GCTGAAGTAACGCTT[A/T]GGTGTTGACAATGAT | 1130 |
rs545260735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820217 | TGAGTCAAAGGGGAA[A/T]GGGCTGAGATCACAA | 1130 |
rs545265263 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235680792 | TTAGTAGAGAAGAGG[C/T]TTCCCCATGTTGGCC | 1130 |
rs545265647 | in-del | -/ATAAC | | | intron-variant | LYST | GRCh38.p7 | 1:235798309 | GGACTTCAGTTAATA[-/ATAAC]ATATCAATATAAGTT | 1130 |
rs545296158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785217 | CTGTTCTTAGATAGG[C/T]CTTCCCTGATCCACC | 1130 |
rs545298000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784302 | ATTAACTTGTGCCAA[A/G]TGGCAAACAATTCTC | 1130 |
rs545324397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235874395 | ATAGTCGAGGGAGAT[A/G]AAGGTTATGGCAACA | 1130 |
rs545333731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235793680 | AAATGAGCAATTTCA[C/T]CAAAAGAGGTAAAAT | 1130 |
rs545371033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714468 | CAATAAGAGTGAATA[A/C]AAATTCATTCCTCCA | 1130 |
rs545381148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666030 | TTCTGTCTTTTATTA[A/G]GACAATGAAAATATT | 1130 |
rs545394405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866531 | CCCCGCGCGCTGCGA[A/G]ATAAAGTTAGTGCCC | 1130 |
rs545414716 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687787 | CTCTCCTCTCCTCTG[C/T]ACCTCAACATGTTTC | 1130 |
rs545415108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770373 | TTGGAAGACACACAA[C/T]GCGCAACAATTTAAC | 1130 |
rs545416692 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235730420 | TTTAATCACTACGTT[A/G]TATTGCTGCTTGATG | 1130 |
rs545451878 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235725410 | CTGCACTCCAGCCTC[A/G]GTGACAGAGTGAGAC | 1130 |
rs545452434 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702293 | GAGGCCAAAGAAATA[C/T]GTAAAGTTCCCCTTA | 1130 |
rs545474480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763339 | GAATCATCTTTTTGC[C/G]CTAAATTTACTCCTT | 1130 |
rs545474488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755431 | AAGAAAAGAAAAGAA[A/G]AAAGACAAAAGATTC | 1130 |
rs545495220 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235816507 | CCAAAGCAATTTACA[A/G]ATTCAATGCTATTCC | 1130 |
rs545497564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235806908 | TATTCATCAATTATC[A/T]GGCTAAAGTTCTTAG | 1130 |
rs545498009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753668 | AGAGGTCTAGCAAAA[C/G]GGAATGATTCTCGAG | 1130 |
rs545504758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235790812 | CAGTTAAAGAAGGAA[C/G]TGGAATGAAATTTAT | 1130 |
rs545524167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235858572 | TTAATCCTGCACTTG[A/G]CTCATTTAGATTCTT | 1130 |
rs545534702 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235742926 | AGAGACTACATTTAC[A/G]TAACTTTTATTAAAG | 1130 |
rs545556404 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235794398 | CTTTATTCCATCATA[A/G]GTTTAGCATAAAACA | 1130 |
rs545566277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871997 | AATTTATTTAATCAG[A/G]GTTTTACGTAACATG | 1130 |
rs545613757 | in-del | -/GAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235681277 | AGGGAAAGGAGATAT[-/GAAA]GAAAGTGGCACTGCC | 1130 |
rs545614020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834956 | GTTTCACCCTTTCGC[C/T]CAGGCTTGAGTGCAG | 1130 |
rs545628014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738805 | TGAAGAATCTTAGGC[A/G]GGTGCACCCAATTTC | 1130 |
rs545628184 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235687302 | AGTCTATGTCTATAC[A/G]TGCCTGTGTGTGGAT | 1130 |
rs545647023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776907 | TAATCATCTATGGCA[A/G]AAAGCTTAATAACAT | 1130 |
rs545647734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761271 | ATTACCATCTCACCT[A/G]CAGTATTTAATAATT | 1130 |
rs545683487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723470 | AATGGCTGGTAAGGT[A/G]TAAGAACTAAGAGAA | 1130 |
rs545686240 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235670274 | AATGGGGAGAGGACA[C/G]AGTAACAGGAGCTGC | 1130 |
rs545703978 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710629 | AGCATTTCCTGTCTT[A/G]CATGCCCTTCCAGAA | 1130 |
rs545715555 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235872591 | CTAGAATCATCCAAC[A/G]GGGGAGGTCAGAGAA | 1130 |
rs545725414 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673498 | ACCAAAAATCAAGGT[C/T]AGACATCCTCAGATG | 1130 |
rs545750606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732009 | GAAATAAATAAGAGA[A/C]AAAAATACCCTTATT | 1130 |
rs545761155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754189 | CCTTTATGTAATCTG[C/T]CACTGAGAATACATG | 1130 |
rs545763141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857402 | GGGTACATCTTCCTA[A/T]ATAAGGATGTTGGGA | 1130 |
rs545793189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848861 | ACAGACCCAGCGAGA[C/T]TGAAATGGTAATTTA | 1130 |
rs545827638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235841397 | TAAGAGGTGGTGCGG[C/T]GTGGCCAGCCATCTC | 1130 |
rs545831563 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235849435 | GGGAAAAGTTGAAAG[C/G]ATTCCCTCTGAGAAT | 1130 |
rs545860213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698656 | GCGGGCGGATCATGA[A/G]GTCAGGAGATCAAGA | 1130 |
rs545868768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841974 | TAATTTACTGGTTGG[A/C]TACTAGCTTAGCAGA | 1130 |
rs545881005 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235705546 | GTGTGCCACCATGCC[A/C]AGCTAATTTTTAAAT | 1130 |
rs545891776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235878948 | TGGATATATTGAGTA[A/G]TGGTGAGGTCTGGGC | 1130 |
rs545900203 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739572 | CAACTATCCAAGTGT[C/T]ATACTAACTAAAACC | 1130 |
rs545928234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235871110 | CTTTTACAATTGTGC[A/G]TCTTGGTAGCCACCT | 1130 |
rs545928296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235729138 | AATAAAATTTTCAAA[C/T]AAATATAACTATATA | 1130 |
rs545945525 | snp | C/T | 1.66704e-05 | 0.00288703 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775002 | TTTCTAATTCATGTA[C/T]TCTTTGTTGGTTGTA | 1130 |
rs545951492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863999 | GTTCCTCATCCTCCA[C/T]CATTCCCCAGGTAAT | 1130 |
rs545954032 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235755263 | GCATGGTGGTACGTG[A/C]CTGTAATCCCAGCTA | 1130 |
rs545966715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738248 | CTCTGGCAAAGACTA[C/T]ACTGTAACTGTAAAC | 1130 |
rs545971466 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235670515 | CTCTTGTGAGGAGAC[A/G]TGTCTCACTGCAGCA | 1130 |
rs545983911 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714981 | CATTTTTATAAACTT[A/G]GACATTTAATTTGAA | 1130 |
rs545990716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795717 | ACAAATTCACTTTCA[A/C]AATATTAGAGGAAAT | 1130 |
rs546006283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235742344 | CCTGTAATCCCAGCT[A/G]CTTGGGAAGGTGAGG | 1130 |
rs546043367 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235839264 | ATATATATATATACA[G/T]TTTTTTTTTTGAGAC | 1130 |
rs546043545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848118 | CTTTCTCCAAGATAG[A/G]TCATATGACAGGCAA | 1130 |
rs546058020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751636 | CAGGCTTTTTTTCTA[C/T]ATAAGGCAAAAGTTT | 1130 |
rs546058355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854186 | CAGGCACTATTGTAA[A/G]CACTCTAGGTAAGTA | 1130 |
rs546058855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235810796 | GAGGCACACCTATAC[C/T]TACTCTAAACACTAG | 1130 |
rs546060497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819669 | TGTTTTGTTTTGAGA[C/T]GGAGTCTCACTCTGC | 1130 |
rs546067886 | snp | A/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716728 | TTGTATGTGTCCACA[A/T]AACGATCTTCTTTTT | 1130 |
rs546100100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713359 | GTAATTTTGTAAGGC[A/T]ATGGTGAGGTCAAAG | 1130 |
rs546110311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663867 | TGTGTTAAGTGGTTG[A/G]CTTTTCATGATGACT | 1130 |
rs546137624 | snp | C/T | 8.29346e-05 | 0.00643898 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744030 | AATTTCTTTCTGAAA[C/T]GGATTGAAAACAGAA | 1130 |
rs546141199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704947 | GTATTCATTTCTAAG[G/T]GAACCCCATGTATTA | 1130 |
rs546146232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701607 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCA | 1130 |
rs546147938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710061 | TGTGCTACATTTTCT[A/C]GTTTGCTGAACACCA | 1130 |
rs546153288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728334 | GTGTCTTAATTTCTT[C/T]ATTAAAAAAAAAGGT | 1130 |
rs546153950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852195 | GGAAGGAAATGCTGT[C/T]AAGGCTTTTAACTAC | 1130 |
rs546167567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831383 | TTGCAAAGAGGAACT[A/G]GACTAATCAGGTTTT | 1130 |
rs546202814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685703 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGTGC | 1130 |
rs546206230 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870890 | TTTTGGAGCTGGACA[A/G]TCTTAATGCCTACTG | 1130 |
rs546208255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692302 | CACACCACTGTACTC[C/T]AGCCTGGGCGATGGA | 1130 |
rs546249648 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235839301 | TCGCTCTGTCGCCCA[C/G]GATGGAGTGCAGTGG | 1130 |
rs546257788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789516 | ATCTACTTGTCATTA[C/T]AATACATGTGACTTT | 1130 |
rs546264174 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235685120 | ATTTCCTCTGCCTGA[A/C]ATGTTCTTTCCTCTT | 1130 |
rs546268400 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235829040 | GAAACCCCATCTCTA[C/G]TGAAAATACAAAAAT | 1130 |
rs546290874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665481 | GCCAGGGGTGGTGGC[A/G]GGCGCCTGTAGTTCC | 1130 |
rs546304501 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769905 | TATTCTATCCCAACA[A/T]AAAGAAACATCTAAG | 1130 |
rs546317523 | snp | C/T | 3.30017e-05 | 0.00406199 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808501 | CATAAATCTGAAGCA[C/T]GTCCTGAGGCAAGCA | 1130 |
rs546354235 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697394 | AGCTCTGTAAGGGCA[A/G]TAATTATTTTACGCA | 1130 |
rs546379976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822492 | AAGTTTCTCAATCAA[A/G]AAGAGCTGCAACAAA | 1130 |
rs546393733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750941 | TACTATTTTACAATC[C/T]CTGCAGGGGCAGAAT | 1130 |
rs546412196 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235759939 | AAATTCTTAAATGCC[A/G]AAACTATTTTTATTT | 1130 |
rs546420201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697044 | CTCAAATCTCACGAA[A/G]GATATATCCAGAATG | 1130 |
rs546450488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235725351 | AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGCG | 1130 |
rs546453532 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235815444 | GAGCAGATACTTAAT[G/T]GATGAGAAGAAGGAA | 1130 |
rs546462627 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235675134 | CAAAAGGGGGAAAAG[G/T]GTCAGAAATAATAAG | 1130 |
rs546467143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829854 | CCTCCAAAAATTTTT[C/T]AAAAACATACTTGAT | 1130 |
rs546486381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709338 | TAATATTAATATTTA[A/G]CTCCCCCACAGCAAG | 1130 |
rs546497185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797454 | TCTATTATCTTCCTC[C/T]CAAAAGTCCATACCC | 1130 |
rs546523817 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846561 | AATTCAGGAGGTTAG[A/T]TATTAAGCTAATCAG | 1130 |
rs546525682 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235811449 | AGGTTTAAATAATTC[C/T]TTATTCAAATTATTT | 1130 |
rs546532056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796640 | GAGGAGTCTGCCCTC[A/C]TGGGTGTGATTCATG | 1130 |
rs546546751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667974 | CCTCCTCCTGTATTC[C/T]TTAAATCACCTCTAG | 1130 |
rs546553244 | in-del | -/ACAACCC | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235846208 | CAGGACTCTGTGTAG[-/ACAACCC]CCAGTACCGGCCTGG | 1130 |
rs546567411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749490 | TGGGATGAGTAGATG[C/T]GGTGCAGGACACAAA | 1130 |
rs546604445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757635 | TCACTTTTTATCATT[A/G]ATTTTTTTGGGCATA | 1130 |
rs546610100 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764499 | TTTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 1130 |
rs546610432 | in-del | -/ATAAGTTCATTAATTATA | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235798322 | TAATAACATATCAAT[-/ATAAGTTCATTAATTATA]ATACATATATCATAA | 1130 |
rs546613361 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660601 | TTAGGCCGGGCGTGG[C/T]GGCTCACACCTGTAA | 1130 |
rs546648463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235765268 | CATTCCATCCTAAAC[C/T]TCCCACTTCTCAATT | 1130 |
rs546649677 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682049 | TAACATGTGGCTCAC[A/G]TCTGTAATGCAAGCA | 1130 |
rs546664580 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235722383 | CTAAGGGGCTTTCTA[C/T]AGAGGAGAGCAGAGA | 1130 |
rs546694527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695703 | AATGGTGCGATCTTG[C/G]CTCACTGCAAGCTCC | 1130 |
rs546694650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689091 | TCAAAGAATTAATGG[A/G]TGAACAAAAATATAT | 1130 |
rs546720500 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235695026 | CATCTGTAAGCTACA[A/C]CATTGTTCAGTCAAT | 1130 |
rs546733020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235836688 | AATAGAAGTGTTCCC[C/T]TGAAACCATTTCTCC | 1130 |
rs546752951 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698329 | GGCATCACTGACGTA[C/T]AGACTATCTTTTAAA | 1130 |
rs546753123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786133 | CAGGATGAAATTACA[A/G]ATTCTGTTCTTTGAT | 1130 |
rs546756453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667092 | TACTTCTGTAAGTAT[A/C]AAAATTTGACAGTTA | 1130 |
rs546776850 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235875592 | GAGTCCTGCCCCACA[A/C/T]AACTGCTTGGTTGTC | 1130 |
rs546846639 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235799862 | TTGTGTGGATCTGAG[A/G]AACAAACGAGATAAT | 1130 |
rs546873232 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235808120 | CTACGTTTTTCTCAG[C/T]TGTATATCTAAAACT | 1130 |
rs546878202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801188 | GATCTAGTGGCAAAA[A/C]TAGTAATTCAGAGGA | 1130 |
rs546880335 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235829178 | ACTGCACTCCAGCCT[-/G]GGCGACAGAGCGAGA | 1130 |
rs546884755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764487 | CTACATTTCTTTTTT[C/T]TTCTTTTCTTTTTTT | 1130 |
rs546901581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860045 | CAAGCTGGTCTATAG[C/T]TTTTCTAGGAATCAG | 1130 |
rs546915172 | snp | A/C/T | 0.000947401 | 0.0217446 | intron-variant | LYST | GRCh38.p7 | 1:235800434 | CTTACCTCACAGAAG[A/C/T]ATGAAACAACTGCAA | 1130 |
rs546926696 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235778669 | TGGGATTACAAGCAT[A/G]AGCCACCGTGCCTGG | 1130 |
rs546945990 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235881548 | GCAGCATTATTCATA[A/C]AAGCCAAAGGGGAAG | 1130 |
rs546949744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235872715 | AGTTCAGGAGTTCGA[A/G]ACCAGCCTGGCCAAC | 1130 |
rs546951425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235807130 | CACACCTGAGGTGGA[C/T]ACCCTGAGGGCAGGC | 1130 |
rs546955674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700669 | TGTCGAAAGTTTCAC[C/T]GTGGTTCAAATAAAG | 1130 |
rs546989832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836155 | ACAAAACATACATAC[A/G]CAAACACTGATTTAA | 1130 |
rs546997816 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235844749 | ATGCAGGACACTGGT[G/T]GGGGGAAGGGGACCA | 1130 |
rs547023930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829434 | TCAAAGTGTTAAAAA[A/G]AATCCATCATATTGG | 1130 |
rs547049819 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882772 | TCCATGTTGGAGATG[G/T]TCAGTTTCATGTGCC | 1130 |
rs547052446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770622 | ACATTACCAACATTA[C/T]TGTTTTTAAATAATT | 1130 |
rs547065168 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235665480 | AGCCAGGGGTGGTGG[C/G]GGGCGCCTGTAGTTC | 1130 |
rs547084635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235785503 | AAAATAGGTTAATCT[A/G]TGTTAAGGGTATATG | 1130 |
rs547107343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235669350 | CCTAGAACTAAATTC[A/G]AAGGAAAACCCTAAC | 1130 |
rs547117487 | in-del | -/GA | | | intron-variant | LYST | GRCh38.p7 | 1:235760647 | TGATACAGAATGTAT[-/GA]GAGAGGGGCCCAGGA | 1130 |
rs547137791 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235858262 | GAAAAGTTACTCAAT[C/T]TCACTGAGCTCCAGT | 1130 |
rs547138377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874764 | CAATCAGTTGACAAT[A/G]AAGAGTTGGAAATTT | 1130 |
rs547139174 | snp | C/T | 3.86115e-05 | 0.00439366 | intron-variant | LYST | GRCh38.p7 | 1:235813111 | AGGCGATAAGACACA[C/T]CAGTTCCTAATGTCT | 1130 |
rs547140546 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883274 | GGTAGCTGCAACGAA[A/G]CTGGTCTCTTCCATG | 1130 |
rs547141370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762273 | TAGTTTCACAGGTGC[C/T]TGAAAGCATTCTTGA | 1130 |
rs547151442 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235673609 | CCACTACTCATCTCT[A/G]TTACTATCCCTACCT | 1130 |
rs547160541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755701 | AAATTAAATATAATA[C/T]ATACAAATCAGTGTA | 1130 |
rs547169022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235707412 | TGGTGGATCACGAGG[C/T]CAGGAGTTTGAGACC | 1130 |
rs547169467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235849600 | TTGCTGATGATATGA[C/T]TGTTTACCTTGAAAA | 1130 |
rs547173744 | in-del | -/ATAAT | 0.00295358 | 0.0383154 | intron-variant | LYST | GRCh38.p7 | 1:235712214 | TATAAAAAAATACAA[-/ATAAT]ACGATTAAGACACAA | 1130 |
rs547177553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738469 | GCTTTCCCAAAAACC[A/G]TGTTATTGGAAGTGG | 1130 |
rs547203126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723658 | TGGTGAGAAGTCTGT[C/T]TGAAGCATTTCAAAA | 1130 |
rs547214349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745913 | GTGGGTGTGGCTAAG[A/G]GAAGGGCAATATGAG | 1130 |
rs547219908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850623 | AAAATCTTCACAATC[G/T]ATACATCTGACAAAG | 1130 |
rs547225020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235747995 | TAAAATAGCAACTGG[C/T]ACATGGTTGGTACTC | 1130 |
rs547285760 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235743217 | CCAAATGCTGATCAA[A/G]TCACCTGTATCTGGT | 1130 |
rs547312637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235880967 | CCCATCTCTACAAAA[A/G]ATAAAAAAATTAGCC | 1130 |
rs547332721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679888 | GTCAGTGTTTCAGGA[C/T]TGATAGTGTCCTCAG | 1130 |
rs547336332 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738992 | GCTGCAATTTTAAAG[C/T]CTTCTGATGTCATAC | 1130 |
rs547337084 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235781577 | GACAACCAAGATAAG[C/T]TTACTAGTCATGATG | 1130 |
rs547342315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713679 | CAGCTAAACGTCCTA[A/C]AATGCACAGGGCAGC | 1130 |
rs547343092 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235722953 | GATGCAGGAAGGCCA[G/T]TTAGGAGGCTACTGT | 1130 |
rs547358241 | snp | A/G | 0.131381 | 0.220067 | intron-variant | LYST | GRCh38.p7 | 1:235851192 | TATATGTGTGTGTAT[A/G]TATATATATATGATG | 1130 |
rs547377797 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785651 | TAAATCTAGACTTCT[C/T]AGCTTGGCATTCAAA | 1130 |
rs547379800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235731369 | GTGTCTTTTTGCTCC[C/T]GAATCCCAGTCTCCC | 1130 |
rs547387120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819723 | TGATCTCGGCTCACT[G/T]CAAGCTCTGCCTCCC | 1130 |
rs547388921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783078 | CTACCCCTAATTTAG[A/G]AATGTTTTAAACTCC | 1130 |
rs547393144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856831 | TGAACAAACTCTAAG[G/T]CATAATGCAGTAAAG | 1130 |
rs547406365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235776527 | ACTGTTGGTGCTCCC[C/T]AACATAGGTTTCAGC | 1130 |
rs547416172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680544 | GTGCTGGGATTACAG[C/G]CATGAACCACTGTGA | 1130 |
rs547427807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705140 | TACAGAGAGGTCAAG[A/G]TATTTGCCCTAAGGT | 1130 |
rs547445738 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235820096 | GTACCAACAAGGTGC[A/C]AGGCACTGGCCCTTT | 1130 |
rs547474137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235810915 | TTGGGAGACTGAGGC[A/G]GGTGGGATCACTTGA | 1130 |
rs547475701 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821208 | TTTGGGAGGCCAAGG[C/G/T]GGGTGGTTGCTTGAG | 1130 |
rs547502542 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235760642 | TCTACTGATACAGAA[G/T]GTATGAGAGAGGGGC | 1130 |
rs547503771 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866815 | GAACCTTCTGCCGGC[A/T]GCGTCGGCGCCCGGC | 1130 |
rs547506467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235706842 | TATATGACTTCAGAC[A/G]TACTCAAAATAATTA | 1130 |
rs547508401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235852152 | TGTGGTCTCCAGTTC[C/T]GTAGATACTAACATT | 1130 |
rs547513698 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235777011 | TCCTTTAATTTATCA[A/G]TAATAAGTAAGTCAT | 1130 |
rs547567202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235799346 | GTCTCAAGTTATCTC[C/T]CCACAAGATACTTAT | 1130 |
rs547586352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842162 | TGAAGGGGACCCAAG[C/G]GTATGGGTGGAAGAA | 1130 |
rs547591009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698434 | GTCTAAAAAATGAGT[A/G]TCTCTGGAAAAGCTT | 1130 |
rs547633110 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685827 | CTCTGGCCTGGGCGA[C/G]AGAGTGAGACTCTGT | 1130 |
rs547654503 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235693113 | AAGGTCAGGAGATCG[A/C]GACCATCCTTGCTAA | 1130 |
rs547663535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235670014 | ACTATGTCAGAAATA[A/G]TAAGTTTCTCTTCAA | 1130 |
rs547672544 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235674358 | ATCCAATTAGCCATC[A/C]CTTTCACCCTGGCAT | 1130 |
rs547676403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235728623 | CTCCAACTTTTTCCT[A/G]TTTCATAGGCTGGCT | 1130 |
rs547691125 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761303 | GGATTGAAGCTAAAG[A/T]CAAGACTAGGTTGGA | 1130 |
rs547722838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677827 | TCATTTTTGTCTATT[C/T]TTGTCCAATCTTTGT | 1130 |
rs547733261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819133 | TGGAATTGTAGTCCT[G/T]AAGAGGGCATCCCAC | 1130 |
rs547738259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796940 | AGATACCACTTCATA[A/T]CCACCAGGATAGATA | 1130 |
rs547738971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864847 | GGTGAGAGGATCACC[C/T]GAGCCTGGGAAGTCG | 1130 |
rs547789657 | snp | C/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740399 | AAAGTTCCCTTAAAC[C/G]TCTTTCCAGTCAATT | 1130 |
rs547805636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811963 | ACCTCCTTAAAAAAA[A/G]CTCCATGAAATTCAC | 1130 |
rs547821564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753802 | CTTTTCTTCTCAAGG[C/T]TATTGTGAGAATCAA | 1130 |
rs547824022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663281 | GAGATGCTCATAAAT[A/G]CGGTGATATAGAATA | 1130 |
rs547832766 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235695546 | GCTTAGAATATGTTT[C/G]ACATGCTTAAGTCCC | 1130 |
rs547838082 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235715428 | GAAAAGTGCTGGATG[-/T]TTTTTTTTCTCTCCT | 1130 |
rs547841690 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235805409 | AGATGGGTGCTGATG[C/T]GCAGATGGTGAATGG | 1130 |
rs547848033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804849 | TTAAAATTAATAACA[C/T]TTTTATTGATAAAAT | 1130 |
rs547883644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692002 | CATGCCCAGCCTAAC[A/G]TCAGATTCTTGACTG | 1130 |
rs547888442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705671 | GGTTATAGGCATTAG[A/C]CACTGTGCCTGGCCC | 1130 |
rs547911314 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235871312 | CGTCCTAACTAGAGC[A/G]ATTCCATCTTGAATA | 1130 |
rs547966356 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235848856 | CCTGAACAGACCCAG[C/T]GAGATTGAAATGGTA | 1130 |
rs547968191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235879159 | TACAGGTGTGAACCA[C/T]CACTACCAGCCATTC | 1130 |
rs547978852 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661494 | ACGGTGATCTAAATG[C/T]AGCCTAGGTATCACT | 1130 |
rs547984434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876534 | TTGAATGAATTCTCT[A/G]TGATCTGTAGCCACA | 1130 |
rs547991432 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660789 | CAGCTACTTGGAAGG[C/G]TGAGGCTGGAGAATC | 1130 |
rs548004390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693126 | CGAGACCATCCTTGC[C/T]AACACGATGAAATCC | 1130 |
rs548013030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235782203 | TTTTTTTTGGAGACA[A/G]AGTCTCGCTCTGTTG | 1130 |
rs548018825 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235737215 | TCAGCAGGATTGTTA[C/T]TAGTGATCATGTTGA | 1130 |
rs548031796 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235671205 | AGCCTCCCAAAGCGT[C/T]GGGATTACAGGTGTG | 1130 |
rs548045158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670564 | TGAGACCCACCAGCA[G/T]GATGAATATACCGAG | 1130 |
rs548068447 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841622 | ACAGGGGCAAGAGAA[C/T]GAATGAATGAAGGAC | 1130 |
rs548071810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803972 | CAATTATGTACCACA[C/T]AATTTTAGGAAAGAA | 1130 |
rs548072544 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235768001 | TATCTCTTTCAATAG[A/C]CCCTTTTTCTGGTTT | 1130 |
rs548101902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872094 | GGAAGTCAGGAGTTC[A/G]TGACCAGCCTGGCCA | 1130 |
rs548107600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803478 | TAAATGCCTTATAAG[C/T]TAGGTAACTAGAGCA | 1130 |
rs548110888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775195 | TTAGTTTCTACAAAG[C/T]ATTTTTTTAATGCTC | 1130 |
rs548112264 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766245 | TCTACAAACCTCTCG[A/G]GGCATGGGTGTGAGT | 1130 |
rs548136460 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884719 | GTCATCTTTTTAATA[C/T]GTCTGTTATGGATTT | 1130 |
rs548183627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744224 | CATTATAAATAGTAA[C/T]AATACTGGTAAAAAA | 1130 |
rs548205734 | snp | C/T | 1.6943e-05 | 0.00291053 | intron-variant | LYST | GRCh38.p7 | 1:235703029 | AGTAAAAAGAAAGAC[C/T]TGACAATAATACCAA | 1130 |
rs548208343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697714 | GCTCCTTGAAGAGAG[A/G]GAACACCTCTGATTC | 1130 |
rs548219298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779840 | AACAGTAGTCTCCTT[C/T]AAGTAAGAAATATCT | 1130 |
rs548242945 | snp | A/G | 1.72305e-05 | 0.00293513 | intron-variant | LYST | GRCh38.p7 | 1:235773824 | ATAAAAAATGGAAAA[A/G]AAGTACATATTACAT | 1130 |
rs548248737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789878 | TTATAGAGTAGTAAT[A/G]TTACAAATATTTAAC | 1130 |
rs548252226 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235800605 | TGTATTAAAATTAAA[C/T]GCATTTTTAAAAATA | 1130 |
rs548252234 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235726665 | GATTTGAAAAAAAAA[A/T]TTTCCTCTTTATTTA | 1130 |
rs548278707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235676092 | TCTTTTCTGCTGGAT[A/G]CATTGGTTTCTTAAC | 1130 |
rs548279228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773311 | CAAAAGAGTAAAACT[C/T]CATTTCAAAAAAAAA | 1130 |
rs548279514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780333 | CATTTGAGCCCAGGA[A/G]TTCAAGGCTGCGGTG | 1130 |
rs548292494 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235873763 | CACCTGAAACCACAC[-/T]TAGCTGTTTATTTTG | 1130 |
rs548345950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852672 | AGGTAAGTGACAAGT[C/T]GATTGACAATAAAGG | 1130 |
rs548350139 | snp | A/G | 7.46088e-05 | 0.00610728 | intron-variant | LYST | GRCh38.p7 | 1:235741658 | GATAGGAATGAATTA[A/G]GATCAGACTGCTTAA | 1130 |
rs548359738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749874 | CTAAAGACTGCTAGA[C/G]AAATCATTGACCAAA | 1130 |
rs548361493 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235730156 | AATCAGAAAGTTCCT[C/T]TGTGTTCTTAGCCAA | 1130 |
rs548369228 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235699141 | ATACATGTGCAGAAC[A/G]TGCAGGTTTGTTACA | 1130 |
rs548388260 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235877567 | ATGCACCACCACATC[C/T]GGCTAATTTTGTATT | 1130 |
rs548409845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853749 | TTGCAGAACAAAGCT[C/G]GCCAGGAAATAAAGG | 1130 |
rs548454914 | snp | C/T | 0.000709647 | 0.0188234 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751178 | AAGCTAGCCTCAATT[C/T]ATGGTTATTAAAATA | 1130 |
rs548455623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883513 | CACCACAGAAACCTC[A/G]GAATACAACTTTCCC | 1130 |
rs548474114 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763108 | CTGTACTTATAGTTA[-/T]TTTCTATGGTTTAAC | 1130 |
rs548493455 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884064 | GGCTCAAGAGATCCT[C/T]CTGCCTCAGCCTCCC | 1130 |
rs548507113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846635 | AAAATGATATAAGAA[A/G]TGAAGGGAGAAATAT | 1130 |
rs548510015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742587 | ATATATATATATATA[C/T]ATCTTACCACAGTTT | 1130 |
rs548525749 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235799507 | AAAAGGACCCAATAT[A/C]ACTTCTGAGTATTCC | 1130 |
rs548589202 | snp | A/G | 1.69112e-05 | 0.0029078 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830410 | AGTGAGTTACTGTCG[A/G]TGCTCATGACCGAGC | 1130 |
rs548605945 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667066 | CAAAACCAAATAACT[A/G]CTCATCTGCCTACTT | 1130 |
rs548656238 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868326 | TAATGAGCACCTACA[A/G]TGCGCTAAGTATTGT | 1130 |
rs548657942 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235835982 | AAGAAAACTTGCCCC[A/C]ACGATATTCGTAGAA | 1130 |
rs548663306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859949 | AGCATGAAGTTAGCT[C/T]AATATGACTTGTTCT | 1130 |
rs548695127 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235823006 | GAGCCAAAGTGGCTA[A/T]TCCAGCTGAGCCATG | 1130 |
rs548717408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794776 | CATGGACTTTATCCT[A/G]TACATAACATGAATC | 1130 |
rs548735607 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235845210 | CTCTCCTGAACACAC[A/C]CCCCCACTGGAGAAG | 1130 |
rs548784562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829323 | ACTGTTTTAGTCTCC[A/G]TATTTCCTCAATATA | 1130 |
rs548814968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689005 | TAATAATAATAATAA[C/T]AATAATAATAATAAT | 1130 |
rs548816408 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790899 | GGGCCACTGAGGTAA[C/G]ACATGGCATGAGAAG | 1130 |
rs548824161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682467 | GCTGTGCAGCCTCAG[A/G]AAGCCCACAGCAGGC | 1130 |
rs548826469 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669660 | TGACGTGAGCATAAA[A/G]TGGCCAATGGGAAAC | 1130 |
rs548840156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235695663 | TTTGAGACGGAGTCT[C/T]GCTCTGTCTCCCAGG | 1130 |
rs548859697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716187 | CTTGATACTCGTGAA[A/G]AATGTAATGCGTAGC | 1130 |
rs548871811 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235733262 | ACAGACCATATTTTA[A/G]AATTAAGCTAATTTT | 1130 |
rs548881540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786371 | CTCACACCAGTTAGA[A/G]TGGCAATCATTAAAA | 1130 |
rs548895404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235724695 | CCTTTCCTCTCCCCA[A/G]TCTCTGGCAACCACT | 1130 |
rs548900649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696262 | TTTCTCTGGGTGCTG[G/T]CACCTTTGTATTGCA | 1130 |
rs548900869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235690150 | GATTTCATTTTTCTT[C/T]ACTTTTCATTGGAAA | 1130 |
rs548908601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | LYST | GRCh38.p7 | 1:235740616 | CCTTTTTAGAGCTGT[A/G]TAATAGTCTATATGG | 1130 |
rs548921744 | snp | A/G | 0.000483708 | 0.0155441 | intron-variant | LYST | GRCh38.p7 | 1:235800303 | CAGAGCTATTGTTTA[A/G]AACAGTTTCAACTTA | 1130 |
rs548951647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785318 | CATTTGTAAATATTC[A/G]TTTAATTGTGTTTGC | 1130 |
rs548957374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235686764 | AAAATGGGACTACTA[A/C]AATTGTTTTCAAGAT | 1130 |
rs548959088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814664 | GCTTTAATGGAGTGA[C/T]TTGACTGCAACTCCA | 1130 |
rs548974489 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235717531 | GGCACTTGAAGGAGC[A/G]AAAGAAAAAGCTCTG | 1130 |
rs548986789 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758491 | GACCTGCATTATAAT[C/T]ACCTGAGTGGAATGG | 1130 |
rs549012254 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235794534 | CTGATCCTCACCAAA[A/G]ACAAAAAACCCTAGA | 1130 |
rs549020781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235682026 | ATCAAAGGGTTATTA[C/T]GAAGATTTAACATGT | 1130 |
rs549025124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235875556 | CTAAGCCAGGGGGCA[A/G]CTACATCATGCTGAT | 1130 |
rs549035565 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235772397 | GTTATATTCTAATTA[A/G]TTCTAGACAATCTAG | 1130 |
rs549063314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792192 | TAATAATCTTGAAAT[C/T]TAGGTTATAAATGAA | 1130 |
rs549070498 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235808005 | TCATTTTCTCATATT[A/C]CAATATGATCTTTGT | 1130 |
rs549075959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700819 | GGACCTTCCTAGGAA[C/T]TGGGGACACAGTAAT | 1130 |
rs549089269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235747755 | TTAATACTAGAAAAC[A/G]TGGGAGGGTATTTCA | 1130 |
rs549091115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235801992 | CGAAGTCAGGAGTTC[A/G]AGACTAGCCTGGGCA | 1130 |
rs549096454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853776 | AAGGAAACTCAGGCA[C/T]AGGGCAGCCAGGCAA | 1130 |
rs549098264 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235677465 | TATGTTTGATTTGGA[A/G]ACCTTCTTCTGTACC | 1130 |
rs549109869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235835275 | TAAAATAAAATTATG[A/G]AAGGGAAATTATGGA | 1130 |
rs549149695 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235689295 | AATTCTTTTATATAC[-/A]ATGAAATATTATTCA | 1130 |
rs549156863 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235792780 | GCAATTCTCCTGCCT[-/C]AGCCTCCTGAGTAGC | 1130 |
rs549161168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812226 | TATATCCTTTAGGCT[A/G]GGCACGGTGGCTCAT | 1130 |
rs549162178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732465 | AGCCACTGTGCCTGG[A/C]CTGCCTTCCATATTT | 1130 |
rs549185007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673710 | GGCTTCTTTGAAATG[C/T]GCTTTGTTTCTTCCC | 1130 |
rs549192083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793771 | GAAGAAATAGCAATA[C/T]AACTAAATGTAAATC | 1130 |
rs549200605 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235722735 | ATGATCTGCCCGCCT[C/T]GGCCTCCCAAAATGC | 1130 |
rs549217194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822449 | TGTATATAGGGCATA[C/T]GCGGAGCAGATAACC | 1130 |
rs549234758 | snp | C/T | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806142 | TCTGAACAGTTTCTG[C/T]ATTATCATAAATATT | 1130 |
rs549239738 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | LYST | GRCh38.p7 | 1:235874488 | AAAGCTTCTTGGAAA[C/G]CAGCCTCTAAACTTG | 1130 |
rs549240109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235777527 | GATCAATTGTATAGA[A/T]CACATCAAGGTTGAG | 1130 |
rs549256760 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235855087 | TTATCATGTTGCTAT[A/G]GAAATTCCCATTAAT | 1130 |
rs549269197 | in-del | -/TTAT | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235778366 | CTTAGATTATTCTTA[-/TTAT]TTATTTATTTATTTA | 1130 |
rs549270831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771512 | TATACATTTATACTG[C/T]TTTTGATCCAATTTG | 1130 |
rs549275763 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828680 | TTACTATTACTGATG[C/T]TATTTATATGGTATA | 1130 |
rs549304749 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829491 | AACTAACTATATTAA[G/T]TAGTTCCCTGAAAGC | 1130 |
rs549311555 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235721504 | CAATTAAATAATGAT[A/T]GCTAATAAATGAAAA | 1130 |
rs549329691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850560 | AGAGCTTTTGCATGG[A/C]AAAAGTAACAGTCAG | 1130 |
rs549349360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761614 | TGGTTAGACTGAGGC[A/G]AGGTTAGCATTTTTC | 1130 |
rs549373796 | snp | A/C | 1.6574e-05 | 0.00287867 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762797 | GACCTTCCTCCACTG[A/C]TGGAATGCCTCAGGT | 1130 |
rs549382148 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235813441 | GTTACTAGAAAAATG[C/T]GAAGCCTTCATGCAG | 1130 |
rs549390175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707307 | TTTTTCTAAAGTTAG[C/T]CTAGCCAACAACATC | 1130 |
rs549411171 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674928 | GTGTACTCATTCTTG[C/T]AAGTTGCTGCATCAT | 1130 |
rs549418201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235671946 | AACAGTTTTGGACTA[C/G]TGTGATAGATGTTAG | 1130 |
rs549420764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235747090 | GCATCATTTGGAATT[C/T]AATGCTACAAAAGCA | 1130 |
rs549435881 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235784738 | TTGAGAGCTCAAGAA[A/G]TTGAGTGGAGAGTGC | 1130 |
rs549472919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783707 | TGAAAGAAAACCTAT[C/T]GCAGGATGAATGCAA | 1130 |
rs549473243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775859 | CAAGGCAGGTTATGC[A/G]TGTAAGGATTTTAAG | 1130 |
rs549484046 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235851630 | GACAAAACAAAGTTC[A/G]TTAGGAATATTATTT | 1130 |
rs549495338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739941 | ACCACTGACAGACAC[A/G]AAGTAGTGGGAAAGG | 1130 |
rs549519304 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235881702 | ACCTTAAAAAGAAAA[G/T]AAATTCTGACACATG | 1130 |
rs549550550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235820281 | ATGGGCACCAGATGG[C/T]TAGGGTTCAAGGACT | 1130 |
rs549551597 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235714545 | GAGTAAAAGAATGGA[A/T]AATGATTCCTCAAAG | 1130 |
rs549563746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680328 | TGGTGTGATTATAGC[C/T]CACTGTAGCCTCAAA | 1130 |
rs549580912 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235824486 | TACTGATGAGGACAC[C/T]GTGCTCTGGAGCAAT | 1130 |
rs549584041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768932 | GAAAGGCAATAAAAT[A/G]TTTTTGTGTTTTTGG | 1130 |
rs549600207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713953 | TAAATTTTAGTTGAT[C/T]GGTAGTTTTATATTA | 1130 |
rs549614224 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235781201 | TAAAGCCTCAATTTC[A/G]AAATTGGTGTAACGA | 1130 |
rs549627033 | in-del | -/GCAGGTGCCCCAAATT | 0.0244538 | 0.107838 | intron-variant | LYST | GRCh38.p7 | 1:235711258 | ATGAAAAGCTTCAAG[-/GCAGGTGCCCCAAATT]GCAGGTGCCCCAAAT | 1130 |
rs549639286 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235670730 | GTATGTGAATGAGAT[A/G]CACAATTAAGTGCAA | 1130 |
rs549641167 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235857718 | ATACACACACACACG[C/T]ATATATACACAAACA | 1130 |
rs549648943 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235782255 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA | 1130 |
rs549667745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797895 | AGAAATCAATATCCA[A/G]AATATATAGAGAACT | 1130 |
rs549670425 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718364 | TGCAAGCATATTCAC[-/T]TTTTTTTTTTTTCAG | 1130 |
rs549677331 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778593 | TGGCCAGGCTGGTCT[C/T]GAACTGGCTGGTCTT | 1130 |
rs549678601 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778435 | GCTGGAGTACAGTGG[C/T]GTGATCTCAGCTCAC | 1130 |
rs549688429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745200 | TTAACATATCTATCA[C/G]CTCACATAGTTACCA | 1130 |
rs549694741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857680 | GTGGGTGTGTGTGCG[C/T]GTGTGCACACAGGTG | 1130 |
rs549718347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863529 | ATTAATCAGATGAAG[A/G]TGTTCAAGTTAAATA | 1130 |
rs549722252 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817645 | GCATGTTCTCACTTT[A/G]TAAGTGGGAGCTAAA | 1130 |
rs549731453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858229 | AAGACTCAGGTACTT[A/C]GTAGCTGTGAGTCTT | 1130 |
rs549736638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721207 | GAAAAAAAAATAAGG[A/G]AAAAAGAAGAGTTTT | 1130 |
rs549752911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738372 | TCATTCCTAATGTTG[C/T]AAAATACAGCCCGAA | 1130 |
rs549783232 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235848729 | AAATACAAAAGATCA[C/T]TCAAGGCTACTACGA | 1130 |
rs549785072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235752452 | ATAGTAAATGGTTGT[A/G]AGTGTAACACTAGAG | 1130 |
rs549789731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833697 | ACATATTAATCACAA[C/T]AGTAAACCACAAATA | 1130 |
rs549795247 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235685933 | TACAGGTTTCACTCA[G/T]TAAAACAGATTTAAT | 1130 |
rs549817332 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819698 | GCCACCCAGCTGGAG[C/T]GCAGTGGCGTGATCT | 1130 |
rs549821163 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235760521 | CATTGTAGTGCATGG[C/G]ATACAAGTGCATGCC | 1130 |
rs549823254 | snp | A/G | 0.000485709 | 0.0155762 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752056 | CAAGCATTACAATAA[A/G]GTCTTCAATAACCCT | 1130 |
rs549827850 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235790128 | CTTAAAATAAAAATT[A/C]AGAAAAAACTTTCCA | 1130 |
rs549828475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235880844 | AGAATTCCATTTAGC[A/G]GCCGGGCACGGTGGC | 1130 |
rs549848463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737915 | GGAGCCGCTGCCGAC[A/G]AGTCTGGATCTCACT | 1130 |
rs549853727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864124 | CATCCACGATCCCCA[C/T]ACTGCTGCTTGGCTA | 1130 |
rs549860428 | snp | C/T | 0.000399281 | 0.0141238 | missense | LYST | GRCh38.p7 | 1:235712156 | GTCGCCAAGTTGTAT[C/T]TGTAGAATGAAAAGT | 1130 |
rs549861092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679811 | TCTCTTGGCACTCCC[C/T]AGCTTGCTTAGTTCC | 1130 |
rs549894161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235722780 | TGAGCCACTGTGCCC[A/G]GCCCTGAGCAAGTTT | 1130 |
rs549898412 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875993 | GGGAGGCTGAGGCAG[A/G]TGGTTCACTAGAACC | 1130 |
rs549920549 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235864995 | TCCACTGAGAGTAGA[A/C]ACTCAAGTCCTTAAA | 1130 |
rs549929280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235727793 | ATATTTGTTGCAACG[A/G]AGGACAGTAATAAGA | 1130 |
rs549944140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235767327 | TAGATGTTAATTTTG[A/G]AACAATTTAGTTCGA | 1130 |
rs549948140 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707788 | TGCTAAATAAATTAT[C/T]CTATAGCTATACTTA | 1130 |
rs549963709 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235698304 | CATTTTCCAAATAAA[A/T]GAAAAAAAAGGCATC | 1130 |
rs550012211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840586 | CCTAAACATCGGTAT[G/T]TTTAACAAGCTTCAT | 1130 |
rs550031524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790904 | ACTGAGGTAAGACAT[A/G]GCATGAGAAGGAGAA | 1130 |
rs550051760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235720276 | CAAGACAACCAACTA[C/T]AAAAAGCTATCTTTG | 1130 |
rs550090494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719433 | GAAGAAATGAGAGAA[C/T]GGGAAATCAACATTT | 1130 |
rs550101109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871224 | CAGATTTGGTTTTAG[A/T]ATGATTCTTTCATGT | 1130 |
rs550114259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736329 | TTCTAAGAAGGAAGA[A/G]TTCTGAGTAGACTAC | 1130 |
rs550123150 | snp | C/T | 0.000526992 | 0.016224 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702775 | TCTTTGACCTGTTCT[C/T]GGGTCTCCCTGAAAG | 1130 |
rs550124116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698701 | ATGGTGAAACCCTGT[C/T]TCTACTAAAAATACA | 1130 |
rs550134731 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235684357 | ATAAAAAGCAAAAGA[C/T]AAAGCCAGGTTTTAA | 1130 |
rs550144040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767823 | CTTGTAAGTCATTAA[G/T]AATTTCTGAGTCAAT | 1130 |
rs550148699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832498 | ATTTAAAAATGTACC[G/T]AAAATATATACATGT | 1130 |
rs550165584 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235824961 | GATGGCAGAGGTTGC[A/G]GTGAGCCAAGGTCGC | 1130 |
rs550166282 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235803505 | AGCAGACAAGACATT[C/T]TTTTCAAAGGGATTA | 1130 |
rs550178701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819095 | TGAGGCAAGTGCAGA[A/T]GTTTGGGTTTTGGCC | 1130 |
rs550179260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670479 | GATCCCATTCTCCTC[C/T]GGAGAAGGGTCTCCA | 1130 |
rs550181852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235774612 | AGCTAAAGCAAAGAT[C/T]TCATCAATCTACAGA | 1130 |
rs550187881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878207 | CATCCCTGGAGCAGG[C/T]GAGCTCGGCCTTCAG | 1130 |
rs550217456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663196 | GGCGCAGAGAGACAT[A/G]AACTAAATGACTGCC | 1130 |
rs550229349 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235768878 | CAATCGACATATTCT[A/G]TTCCCTACAACAATA | 1130 |
rs550275305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697836 | GATTAGAGAATCTCT[A/G]GCCAGTACTAGAGAA | 1130 |
rs550281960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853684 | CATGCCATTCCGGCT[G/T]CCTTGAAACCTGGGG | 1130 |
rs550282403 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235765393 | TTATTCCTGAATTCT[A/G]CTGCAATAATTTACT | 1130 |
rs550329846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804194 | TTTAATACACTATCA[C/G]GTATATGTAAAATAT | 1130 |
rs550339130 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667939 | AGTGCAGGGATTACA[C/G]GCATAGCCACCGTGC | 1130 |
rs550341879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668832 | ATCATCAATCATTTG[A/C]GCAAACTTGTACTAC | 1130 |
rs550356732 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235872758 | CATCTCTACTAAAAA[G/T]ACAAAAAATTAGCCG | 1130 |
rs550371758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824522 | GACTAAAGTCACTCA[C/T]CTAGTTGATACGGGT | 1130 |
rs550391032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235815967 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 1130 |
rs550392967 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235694601 | CAGCATAGTGAAAAT[A/G]GGCAATTCACAGCTT | 1130 |
rs550393016 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869721 | TCATGTCACATCTCT[A/G]CTCAAAAATCTGCAT | 1130 |
rs550396603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691955 | CCCGCACCTTGGCCT[C/T]CCAAAGTGCTAGGAT | 1130 |
rs550401574 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884247 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 1130 |
rs550420417 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235727218 | ACCTCCGCCTCCTGG[A/G]TTCAAGCGATTCGCC | 1130 |
rs550424709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795810 | CAACCTAAATCAGTA[A/C]AAATAATATTTAAAA | 1130 |
rs550427813 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808865 | TCCCTGCAGTGTCTC[C/T]TCTAATTGGGCTAGT | 1130 |
rs550441339 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832055 | GTATCGTTTCTGGGA[C/T]TTTCCTTCAAAGCTA | 1130 |
rs550445175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743599 | TTAGGCCAAGATCTA[A/C]AATTCATAATAATTA | 1130 |
rs550446772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669429 | ACTCCCACGTTTTCT[G/T]CTGGCAGATGGGAAA | 1130 |
rs550458900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702302 | GAAATATGTAAAGTT[A/C]CCCTTAGGTATAAAC | 1130 |
rs550460487 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859515 | GCCTTTTTTTTTTTT[A/T]AAATGTATCTATATC | 1130 |
rs550461793 | snp | A/G | 6.64938e-05 | 0.00576563 | intron-variant | LYST | GRCh38.p7 | 1:235774013 | AAAATTAGCATTAAT[A/G]TAAGATGCATTAGTA | 1130 |
rs550465065 | snp | A/C | 1.64895e-05 | 0.00287132 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809292 | CGGTGATGATGCATA[A/C]AATGAGAATATTCAC | 1130 |
rs550473646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235718259 | AAAATTACAGTTGAG[C/T]AAACAATAAACTAAA | 1130 |
rs550492257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823708 | GTGTTTTCTCTAGCC[A/C]CCGTGTTTTTTCATG | 1130 |
rs550529831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742827 | GCAGTACCCCCTTAC[C/T]TGTGGTTTTGCTTTC | 1130 |
rs550534812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773246 | ATCATCTGAGCCTGG[C/G]GGTGGAGGTTGCAGT | 1130 |
rs550537115 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837334 | ATGCTATCAAAAATT[C/G]TGAGAGAAAGCTGGC | 1130 |
rs550542101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235693054 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 1130 |
rs550569606 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660645 | GGAGGCCAAGGCAGG[C/T]GGATCACGAGGTCAG | 1130 |
rs550589550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682091 | TGAGGCAGGAGGATT[G/T]TTGAGCCCAGGAGCT | 1130 |
rs550605465 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729920 | AAGTTATTTAAAAGA[G/T]ATATCAATATTTTAT | 1130 |
rs550610137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786321 | ATAGTAAATTTTTCA[A/G]AGAAATGCAAATCAA | 1130 |
rs550616013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675332 | ATCATAGTTAGAAAA[A/C]TTTAAGTCTTAGCCA | 1130 |
rs550617542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750153 | CAGGAAGCTGAGCAC[C/T]AATGCTAGAACTGAT | 1130 |
rs550673360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778980 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 1130 |
rs550691000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235686455 | GTCTTATTTTTTCCC[A/G]TTTTATGATTCAACT | 1130 |
rs550723133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709386 | GCAGGTCTTAAGAGT[C/T]CACAAAAATAGCTGT | 1130 |
rs550746898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762197 | CAGTATTTGAAAATG[C/T]TTCAGAGTGATGCAT | 1130 |
rs550772981 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235883912 | CATTACTCTTGGTTT[A/G]AGAAGTCTGCAGTCC | 1130 |
rs550781279 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235784108 | TGGTCTTGAATTCCC[A/G]TGCTCAAGCAATCCT | 1130 |
rs550781966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756536 | GCTCAATACTAGGTT[G/T]TATTGCAAGTGATTA | 1130 |
rs550784240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764582 | TCACCTAACTGCAAC[C/T]ACCGCTTCCCGGGTT | 1130 |
rs550811738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876502 | AGGAAGCTGATGACA[C/T]AGAAGAATATAAATA | 1130 |
rs550845111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785574 | GAATTAGATGATGTA[C/T]ATAAAGCACCTAGCA | 1130 |
rs550848012 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235802809 | ACTTGTTAAACTGTA[A/C]GGCAATACAAAATTC | 1130 |
rs550852070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758342 | ACAACGCCTAGGCAA[C/T]GTCTGTCATAACATG | 1130 |
rs550853083 | in-del | -/ATGCCCAGAC | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235670102 | TTAGCAAACCTCTAT[-/ATGCCCAGAC]ATGCCCAGACTTGTT | 1130 |
rs550873683 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235795747 | TCTCCAACAGTTTTA[C/T]TAAATATAAATGGTC | 1130 |
rs550887042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852808 | TCCCTCAAAATTTTA[C/T]AGATAAACTAAGGCA | 1130 |
rs550892545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235860982 | GTCTGGCTTTTTTTC[A/G]TGCTGTGTAATTATT | 1130 |
rs550895715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851985 | CGTGGTATGTTCAAC[C/T]TTCATTGAATCTATT | 1130 |
rs550920752 | snp | C/T | 0.000194148 | 0.00985071 | intron-variant | LYST | GRCh38.p7 | 1:235830166 | TGTAATCCAAAACCA[C/T]GTAGCTACAGTTAAC | 1130 |
rs550959444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762890 | ACAGCAAAATTTTTA[A/G]AAAGGATAAAACGAA | 1130 |
rs550968791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829921 | TAAGATACAGGGATA[C/T]AAGATTATGTCTTAT | 1130 |
rs550999108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235733444 | AATACAAATTCCGTT[C/T]AACATCAATATCTTA | 1130 |
rs551012491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801961 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 1130 |
rs551018815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755895 | CTGGCATTTTTAGCT[A/G]AGCATGGACACCTGG | 1130 |
rs551020778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763647 | TTTTTTAAGGAGAGA[C/T]GAGGTTTCGCTATGT | 1130 |
rs551030215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875671 | GGCAACATGGCAAGA[C/T]CCTATCTCTACAAAA | 1130 |
rs551113830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801380 | ACATCCCATGGACAC[A/G]ACTTTAAAAAAAAAA | 1130 |
rs551120518 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235822353 | TGCTGACTGGATTTC[A/T]GGACTGCTATGGCCG | 1130 |
rs551128172 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235851282 | ACTGGAGACTATTAT[A/T]CTAAGTGAAGTAACT | 1130 |
rs551136147 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235723784 | GAGTTTGTCAAAGAT[A/G]GACCCTGCTACAGCA | 1130 |
rs551143460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235731523 | TTAGGTAAATTTTTT[C/T]TCCAAATTAATTTTT | 1130 |
rs551176570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235835169 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 1130 |
rs551182756 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739033 | TCTAGGCTACAATAG[G/T]ATTTTAGTTGGAGGT | 1130 |
rs551206080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844836 | TAAGCCAGTTAAAAC[A/G]TATCAGTTGAACTGT | 1130 |
rs551208350 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235796674 | TTATGAAAGGGGGAG[C/T]TCAGCCCCCTTTTGC | 1130 |
rs551224676 | snp | C/T | 0.000148523 | 0.00861624 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805880 | ATAGCTTTGCTTCCT[C/T]GGGAGCGGCTTCAGT | 1130 |
rs551264148 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235833632 | ATTTGGACTCATAAA[C/T]TAGATGAAACAAATA | 1130 |
rs551269484 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701678 | GTAGTTAAAAATAGT[G/T]ACCCTGGTAATTACA | 1130 |
rs551270055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739718 | GAATGAGAGACTTAG[A/G]GAAATCACTATTTTG | 1130 |
rs551274994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873648 | ATTGAGCATAATTCT[C/T]AGCCAGGTGATTTAC | 1130 |
rs551279461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695534 | CAAATAAGATAGGCT[C/T]AGAATATGTTTGACA | 1130 |
rs551300927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235740804 | ATATGTTTTAATTTC[G/T]TTTTCAGGTAAATAT | 1130 |
rs551304416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827891 | AATCCAATAGACTTG[A/G]TTCCAGAATACATAA | 1130 |
rs551320004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698946 | GCTAAATTTTAGTTA[C/T]AATTTATCATTCACA | 1130 |
rs551326055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849127 | TCCTTAACAAAATAC[G/T]AGCTAACCAAATCCA | 1130 |
rs551327432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715435 | GCTGGATGTTTTTTT[C/T]TCTCTCCTTCTCTAC | 1130 |
rs551334881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845083 | AGAACAAACCAGCAA[A/T]CCCGAGAGGACCCAC | 1130 |
rs551339925 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235748978 | ATCTCAGTAGTTTTC[A/G]ACAAATGCTAAATGA | 1130 |
rs551341555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716946 | ACCATTCAAAATTAT[A/G]ATTTCAGAAATTAAG | 1130 |
rs551343101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836175 | CACTGATTTAATGTA[C/T]TAGCTACCTCTCATT | 1130 |
rs551350186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235821302 | ATTAGCTGGGCATAG[C/T]GATACATGCCTGTAA | 1130 |
rs551377615 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789926 | CTTATAAGGTAAATA[C/T]ATATAGGGTGACAAA | 1130 |
rs551424734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813732 | GGGGTGGTAGAAGCA[A/T]TCAGTTTAGGAGTTC | 1130 |
rs551429941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827163 | GGGGCCAGAAGTTTG[A/G]GACCAGCCTGGCCAA | 1130 |
rs551442255 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235799392 | AATAGTAACTTTACA[A/G]TAGAGAAACTTGGCA | 1130 |
rs551465989 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235780786 | AAATCTTTAGAAATC[C/T]AATTCATAACTATAC | 1130 |
rs551466730 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235707342 | AGTATACTTGAAAAT[A/G]TAGGCCAGACATGGT | 1130 |
rs551468865 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806685 | AGTTTCAAATGCTTT[C/T]AGAGAATGACTTCGA | 1130 |
rs551468957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235814611 | TGTGACATGATGGCC[A/G]AAAAGCATTTAGTAA | 1130 |
rs551478546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746017 | TCTGCAAGATTCATG[G/T]GGGAAACTGGGTAAA | 1130 |
rs551491071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858818 | TGGGGAAGGGGAGTG[G/T]TCCAAGTTCAGTCTA | 1130 |
rs551500359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842265 | AGACAAGCAGAAAAT[C/G]CAGGCAATCAAGGAA | 1130 |
rs551501585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700191 | GCAAAGATTTCATGA[C/T]GAAAAGGCCAAAAGC | 1130 |
rs551505705 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235807249 | AATCACACTAGAGCT[A/G]AAAATCTACGGAAGG | 1130 |
rs551508015 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823886 | CTATCTCTTCAAAAG[C/T]GAAGAGCTCCTGGTA | 1130 |
rs551515121 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235753845 | ACAATTGTTTCGTGA[A/C]AGCCAAAAGTTGTAT | 1130 |
rs551546424 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235721193 | CACAGATACTAAAAG[-/A]AAAAAAAATAAGGAA | 1130 |
rs551552105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819279 | ATTACTTTTTTATTA[A/G]TATCTGGGTATCATT | 1130 |
rs551606798 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828388 | CTACACTAAAAGCCA[C/T]TGAATTGTACACATA | 1130 |
rs551651241 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | LYST | GRCh38.p7 | 1:235783940 | GCTGAAGTGCAGGGG[G/T]GCAATCATGGCTCAC | 1130 |
rs551651242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792948 | GGATTACAGGTATGA[A/G]CCATGGCGCCCTGCC | 1130 |
rs551653417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705854 | TGGAGTGCAGTGGCA[A/T]GATCTTGGCTCACTG | 1130 |
rs551658011 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712888 | CAATGATCAGACTTT[C/G]TAGCCATAGGGAAAG | 1130 |
rs551660478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235663327 | AGCTCAGTACATTCT[A/G]TTCTTTGCATATCTT | 1130 |
rs551661113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812850 | TTTTCATATTTAGTA[A/T]GAATAAATCACAATA | 1130 |
rs551671748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712714 | GGGTGCGTAGGTTAC[A/G]GTGCATTGTTTTTTG | 1130 |
rs551688990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721429 | GAAAACATATATAAA[C/T]TCTTTTTTAGAGATT | 1130 |
rs551716222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235680657 | AGGCTGGAGTGCAAT[A/G]GCGCAACCTTGGCCC | 1130 |
rs551728435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670665 | GGTAAGAAAAGCCGC[A/C]GGGGCAGTGAAGTAC | 1130 |
rs551752345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235849665 | ATAAAAGAATTCAAC[A/G]AAGTTTCTGGATACA | 1130 |
rs551759277 | snp | C/T | 3.30562e-05 | 0.00406534 | intron-variant | LYST | GRCh38.p7 | 1:235723996 | CCATGAGCACTTAAA[C/T]AATATATATCAATTA | 1130 |
rs551784632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685319 | TGCCTGGATCACTGC[A/G]GTGGCCTTCTCGTTG | 1130 |
rs551792102 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671941 | TAGGTAACAGTTTTG[C/G]ACTAGTGTGATAGAT | 1130 |
rs551792897 | snp | C/T | 0.000577648 | 0.016985 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806074 | CTGTTTAAATCCTGG[C/T]TTTCATTTACACTTG | 1130 |
rs551802943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789944 | ATAGGGTGACAAAAT[C/T]GAGGTGCTGAGAGGT | 1130 |
rs551807477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746801 | GGCAAAGTTCGAGTT[A/T]AAAAGTATTAAATGG | 1130 |
rs551807538 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703797 | GCAGTACATGTGCAG[C/G]TTTGTTATTTGGGTA | 1130 |
rs551813790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856928 | CTCTTACAAGTTACA[C/T]AGGATATACTGATTT | 1130 |
rs551814987 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235666968 | ATAAAAAATCTAAAT[A/G]TGGGCCTGGACTCTC | 1130 |
rs551828726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762175 | AAGAAATGGAGCCAT[A/G]ATTGTACAGTATTTG | 1130 |
rs551872884 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235663484 | TATTTCCCTAAAAGA[A/G]AAAAGGAAAAAAATG | 1130 |
rs551883447 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875717 | GGCATGGTGACACAC[A/G]CCTGTGGTCCCAGCT | 1130 |
rs551926296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722177 | TGGAGTAGACAGAGC[A/G]AGGGAGAGAACAGCA | 1130 |
rs551931074 | in-del | -/CAAAA | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235864928 | AGTGAGATCCTGACT[-/CAAAA]CTAAAAATAAAAGGT | 1130 |
rs551938902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826881 | AGAGATGGGGTTTTG[C/T]CATGTTGCCCAGGCT | 1130 |
rs551956830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775276 | TAAACTCCATGTTCT[A/G]TAGTCTCTTATATAT | 1130 |
rs551966253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872164 | AGCCAGGCATAGTGG[C/T]ACATGCATGTAGTCT | 1130 |
rs551974505 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235820608 | ACTCCTGGGCTCAAG[A/C]AATCTGTCTGCCTTG | 1130 |
rs551981865 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235852483 | GCCGGACCTTTTTCC[C/T]GGGGAAGTCTCACAA | 1130 |
rs551982037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235759779 | TTTCTTAAGAGACAG[A/G]GTCTTGCTCTCTTAC | 1130 |
rs551983483 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235776934 | CATTTTAATATGTAA[-/T]TTTTTTTATGTTAAA | 1130 |
rs551985148 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235870185 | TGGGTGGCATTGGTG[-/A]AGAGTTGACACAGTT | 1130 |
rs551991791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775794 | AAGTTCACAGTACAT[C/T]TAGGAAGCTGCAGGT | 1130 |
rs551995504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782210 | TGGAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGT | 1130 |
rs552039386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797775 | AAAAAAATAGATAAA[C/T]TGGACTTCAAAATGA | 1130 |
rs552051150 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235878451 | TGGACACATGTTCCC[C/T]AATAGTCAGATACTA | 1130 |
rs552060358 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235677281 | AGTCTATGTACCTAT[G/T]GTACATAAGGCATAC | 1130 |
rs552078216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235797071 | GACAACAGTCTGTCA[A/G]TTTCTCAAATGATTA | 1130 |
rs552079061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235751897 | CTATTACAAAATTAA[C/T]GTTAAACTTTTAGTA | 1130 |
rs552082513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235713831 | GATGAAAGTGAATGG[A/G]GACTGAGGTAGTCCT | 1130 |
rs552121193 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845499 | CTGGCCAGAACTCCG[A/G]GGAGGGTGCAAATCC | 1130 |
rs552121774 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807619 | CCACACACGAAGATA[C/T]TGATAGGTTATTTTT | 1130 |
rs552121882 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674603 | TTATAATCAACAGTG[A/G]TTTGCTAACTATACT | 1130 |
rs552139999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865758 | TAGATGAATCTAGGC[A/G]TGGAATTTTAAAATA | 1130 |
rs552144859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744250 | AAAAATATTGTATTT[A/G]ATTACTAATTCAGTT | 1130 |
rs552153444 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235667913 | GTGATCTACCCACCT[C/T]GGCCTCCCAAAGTGC | 1130 |
rs552169424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692160 | TAACATGGTGAAACC[C/T]CGTCCCTACTAAAAA | 1130 |
rs552175379 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235787948 | CTTAATAAAGGAGAT[A/G]GTATAAAAGGACAAG | 1130 |
rs552178978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840466 | TACACTATGCTAAGA[A/C]CCTTGGGCTTTAATC | 1130 |
rs552185110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737789 | CAAATACAAGAATTA[A/G]AGGCTACTAGGGGCA | 1130 |
rs552197699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848326 | AATTAAAAAATTCTT[C/T]GAACTGAATGACAAT | 1130 |
rs552200751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833444 | GTATGAATAAACCAC[A/C]AACTATACATCCATC | 1130 |
rs552217019 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235665577 | AGATAGTGCCACTGC[A/G]CTCCAGCCTGGGCGA | 1130 |
rs552236003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698643 | TTGGGAGGCCGAGGC[A/G]GGCGGATCATGAAGT | 1130 |
rs552251706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870707 | CACCCCTGTTTAGAC[C/T]ATGGGCTCCACAAGG | 1130 |
rs552252336 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235708225 | TGCTTTCACTATTTA[-/T]TTCTGGATGGTGATA | 1130 |
rs552263101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719310 | GGAGTGAGCCACCAC[A/G]CCTGGCCAACTTCTG | 1130 |
rs552279076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879337 | ATAATAGATGTCTGA[A/C]AGCAAGACAAATCTT | 1130 |
rs552309709 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | LYST | GRCh38.p7 | 1:235816741 | ATGGAACAGAATAAA[A/G]AGCCCAGAAATAAAG | 1130 |
rs552315252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871614 | CTGATCACAAGTCTT[G/T]GTAATAAAGTACACT | 1130 |
rs552335254 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235695925 | CAGGCTTGAGCCACC[A/G]CACCCAGCCTACTGT | 1130 |
rs552337429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743513 | GTGACCCGCAGAAAC[A/C]CAAGTGAGATGATGA | 1130 |
rs552339166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735362 | ACTCGCAAACCCCAC[A/G]CAGACAATTCTATGT | 1130 |
rs552349495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235671855 | TTATGAAATATAGAG[C/T]TACAGTGTGAAAGTT | 1130 |
rs552376093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235742688 | AATTAAAAAAAAGCA[C/T]CAAAGAACAATGATA | 1130 |
rs552391792 | snp | C/T | 0.000428371 | 0.0146288 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810223 | TAGCTTTGGGGTGGT[C/T]TTGTTTAGGAAACGA | 1130 |
rs552403287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847662 | TTCAGGATACTCACC[A/T]AACACATAAGCACTC | 1130 |
rs552403305 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235762940 | ATCATTAAATTCAAA[C/T]TTTGACAAAAAGATG | 1130 |
rs552403565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752734 | TCTTAATCTTGATAA[A/T]CTACCTCAATGTACG | 1130 |
rs552465453 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235727993 | AACTCTAATAGTTCT[C/T]CCTTCTCTCTAGTTA | 1130 |
rs552469117 | snp | A/G | 0.000281893 | 0.0118687 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804641 | GGTCCCTCATTTCAA[A/G]TAATATACTTTCCAC | 1130 |
rs552491042 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235695119 | AACACTGACCTCTCC[C/T]AGACCCTAGGGTATT | 1130 |
rs552515466 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235844965 | CTAACTAAAGAGAGG[A/T]GCTCCTGGGATCATG | 1130 |
rs552531389 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235669694 | CGCAGGGTATTTGTA[A/C]CCAAGAAGATTCTAT | 1130 |
rs552538844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690955 | AGAGTCTCGTTCTGT[C/T]GCCCAGGCTGGAGTG | 1130 |
rs552544434 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235740970 | ACTCTGAAATTCTTT[C/T]AGGTATTTTGGGTTT | 1130 |
rs552544780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848297 | CATTGGGTCAAAAAC[A/G]AAATCAAGATAGAAA | 1130 |
rs552572209 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235780414 | GTCTCTTAAAAAAAA[A/T]AATAAAAAATAAAAA | 1130 |
rs552580661 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884829 | ACAGGGTCTTGCTCT[A/G]AAGCCCAGGCCAGAG | 1130 |
rs552585136 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235721260 | TGTAGTAGAAACAGC[-/A]CGGTCTTCTGAATTG | 1130 |
rs552590220 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235792853 | ATTTTTAGTAGAGAC[A/G]GGGTTTCATCATATT | 1130 |
rs552601776 | in-del | -/AAG | 0.00046534 | 0.0152464 | cds-indel, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808804 | TCCCTTGAAATCTGT[-/AAG]AAGGACTGGATAAAC | 1130 |
rs552608382 | snp | A/G | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733665 | TTAGATATATCCTTT[A/G]ATTTTGAATCCAGAC | 1130 |
rs552610056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235741821 | ATACAACATTCATAG[C/T]AGCATCACTCAAAAT | 1130 |
rs552631533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235817066 | GCGGCCAAAGGACAC[A/G]AACAGACACTTTTCA | 1130 |
rs552647957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676720 | GTTAAAATTTTGTTC[C/T]TTCACAGGAGGAAGG | 1130 |
rs552658445 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235876864 | AATTTAGATGGTACG[-/A]GTTATACGGGTCCTG | 1130 |
rs552690643 | in-del | -/T | 0.395635 | 0.2032 | intron-variant | LYST | GRCh38.p7 | 1:235782181 | AACAATGGGGAATTC[-/T]TTTTTTTTTTTTTTG | 1130 |
rs552699029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235703173 | GTGAACAAAAACAAC[A/G]TATCTTGACTGATGG | 1130 |
rs552700896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235712048 | ATTAAAAATAATTTA[C/T]TGCTATACCTTCACG | 1130 |
rs552718126 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | LYST | GRCh38.p7 | 1:235837621 | AAGAGTGAGACCCTG[C/T]TTCAAAAAAAAAAAA | 1130 |
rs552741276 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744116 | TGCTTTGAGTTACAT[C/T]TTCTGGAGTTCTCAA | 1130 |
rs552751942 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LYST | GRCh38.p7 | 1:235708216 | GTCTAAAGGTGCTTT[C/T]ACTATTTATTTCTGG | 1130 |
rs552756164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795737 | TTAGAGGAAATCTCC[A/G]ACAGTTTTATTAAAT | 1130 |
rs552756299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787012 | TGTAACAAACCTGCA[C/T]ATTGTGCACATGTAC | 1130 |
rs552775070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814749 | GACTACTCCTTCTGG[G/T]GTCCTGGTTGTGAAA | 1130 |
rs552794714 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883547 | TAAGAATGAATAAAC[A/G]CTGAAAGAGGCCAAA | 1130 |
rs552831185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837019 | AACAGTGCTGTTCAC[C/T]GGAGCTTTCTGAGAC | 1130 |
rs552841113 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769036 | CAAAACAAAACAAAA[A/G]CCATATCCCTGCTTT | 1130 |
rs552860549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684046 | ATAAAAATTAGCTGA[A/G]AAATCTGCTTTAAGG | 1130 |
rs552923802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683292 | TTGAATGAAGTAATA[C/T]TACCTTGTATAAGCT | 1130 |
rs552928385 | snp | C/T | 0.000890531 | 0.0210825 | intron-variant | LYST | GRCh38.p7 | 1:235730999 | CATAGTTCTCTGCTA[C/T]ATTTATATGTTGAGT | 1130 |
rs552934742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836363 | ACATACACTATAATG[G/T]CAGGTCATGTTAATT | 1130 |
rs552937747 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235666511 | ACAACACTGTTAATA[C/T]AATTAATGCCACTGA | 1130 |
rs552956168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807418 | GCCAGCTAGGTGATT[A/C]TCAGCCCTTTCATCA | 1130 |
rs552958283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756910 | AATTTGATAGTACAC[C/T]GAAGAAGAGATTTCC | 1130 |
rs552961979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820692 | GTATTTCTGATATTA[C/T]ATTAAATCTGTATCT | 1130 |
rs552966761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235794085 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTTCA | 1130 |
rs552980871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235859133 | GATACTAACTTATAT[C/T]TATATCTACCCCATT | 1130 |
rs552982165 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235680750 | ATTACAGGCAGCTGC[C/T]ACCACGCCCGGCTAA | 1130 |
rs552985897 | in-del | -/AAC | 0.00644375 | 0.0563946 | intron-variant | LYST | GRCh38.p7 | 1:235825034 | CAAAAAAAAGAAAAC[-/AAC]AACAACAACAACAAC | 1130 |
rs552991055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801519 | GAATGATCAATTTTG[C/T]CTTCTTCATAAGTGA | 1130 |
rs553000575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235821566 | GTCAGGATAGTTATA[G/T]GTACTGTTTTTCCCA | 1130 |
rs553018401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778546 | CGCCCAGCTAATTTT[A/G]TATTTTTAGTAGAGA | 1130 |
rs553042932 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235765270 | TTCCATCCTAAACTT[-/C]CCACTTCTCAATTTA | 1130 |
rs553069993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681317 | ACTGGGAGCAGGGTA[A/G]GTAGGGAGCAGGAAG | 1130 |
rs553076850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732618 | CAGCTAATATCCTGC[A/G]GTGAATATTAGCAGC | 1130 |
rs553100695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714966 | TTAAAAAGTGAATTG[C/T]ATTTTTATAAACTTA | 1130 |
rs553122669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813990 | CAGATGAGAGAGATG[A/G]TGACTTTCTGAAGTA | 1130 |
rs553124105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235689663 | TATTCTCATCACACA[C/T]GTAAAAAATGCTAAC | 1130 |
rs553128147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794907 | GGATATATACACTTG[C/T]TTCTGTGTACTACTG | 1130 |
rs553173330 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235797996 | TTCAAACAAGATATA[A/C]GAATGGCCAATAAGT | 1130 |
rs553228841 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235861289 | TTTCTTGATTAAGAT[A/C]ATCAATTTTAAGCAT | 1130 |
rs553228928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694779 | CATGATGCCTGGCAT[A/G]CAGCAAGTGCTCCAT | 1130 |
rs553237396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235756152 | TCCACCCTTCTCTAG[A/C]ATCTTAAATGCAACA | 1130 |
rs553238600 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235831796 | AATATTGGTTCTTTA[C/T]ATGCTTTCAGAAAGT | 1130 |
rs553245799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687950 | CTACAAGTGTGTTCA[C/T]GTCTCTGCTACCTTA | 1130 |
rs553254549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841949 | GGGAAAGTAGTGATG[A/T]CAGACAAAATAATTT | 1130 |
rs553263791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700432 | CAAAGGATATGAACA[C/G]CCACTTCTCATAGAA | 1130 |
rs553278406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792350 | GACAGAGTCTCACTC[C/T]GTTGCCCAGGCTGGA | 1130 |
rs553284338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776882 | AATATTCATAAATTA[G/T]AAGAAACCTTAATCA | 1130 |
rs553291243 | snp | A/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806209 | AACTGTTTCTGGAAC[A/T]CTGAACTCAACATGT | 1130 |
rs553317135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235723277 | TGGAGACATCAGTCG[A/G]GAGTTACAATATGTG | 1130 |
rs553321968 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235750283 | GGGCAGTAAGTTTAG[C/T]TACATAGATGTTTTA | 1130 |
rs553355632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235731860 | CCCTCACCTGGCCTC[A/G]TTTTGCCTACTCTCT | 1130 |
rs553383687 | snp | C/T | 8.24545e-05 | 0.00642032 | intron-variant | LYST | GRCh38.p7 | 1:235787197 | TCTCAAAATGCTTCC[C/T]ACCTCTGTCCAGAGA | 1130 |
rs553397035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663839 | TTGCTGCTGGGTCAC[A/G]GACAACCCGCTGTGT | 1130 |
rs553408430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693911 | CTAGAGTGGAAGCAA[C/T]ACCTAGCCTGAGAAG | 1130 |
rs553453654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673131 | ACCCGAGTCAAGAAA[C/G]CACTGCCCTCTTCAA | 1130 |
rs553455878 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867133 | GAAGGCAGGGGGGCG[C/G]GCCGACCCGCGGGGC | 1130 |
rs553476057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811544 | AGATAGGGCCTGGCG[A/T]ATGGTCAACACTCAG | 1130 |
rs553483521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770984 | ATCTTATTATCCTAA[C/T]TGACCTTTCAATAAA | 1130 |
rs553500607 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235756039 | TCTATATCTATATCT[A/G]TATCTATATCTATAT | 1130 |
rs553528250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772182 | GGGAGCCAAGATGGT[A/G]CCACTGCATTTTAGC | 1130 |
rs553532843 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235672094 | TTGACCTGTCAACTG[C/G]GTGAATTCTGAAATT | 1130 |
rs553534007 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235675016 | TCTCGATTCTCCCCC[A/G]CCCTACTCAAATAAG | 1130 |
rs553571396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850002 | AAATACCACTATCAT[C/T]CTTCACAGAATTAGA | 1130 |
rs553594078 | snp | A/C | 0.000212157 | 0.0102972 | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747188 | CTCCAGGAGGTACAA[A/C]ACAGGTAGTGCATCC | 1130 |
rs553599643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879735 | CTAACTTCCTTTCTT[C/T]CTTTCTTTTTTTTTT | 1130 |
rs553600044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738790 | TGGCAGAAAGTATAA[G/T]GAAGAATCTTAGGCG | 1130 |
rs553619512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784172 | GGCATGAAGCACCAT[A/G]CCTGGCCTAGAAATT | 1130 |
rs553626522 | snp | G/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235775937 | GGTTTATAAGTTTTA[G/T]ACTTAAAAACATACT | 1130 |
rs553630832 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235768236 | GTTTTTCTGGTCTCC[C/T]GGCTTGAAATTTTAT | 1130 |
rs553636817 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235880398 | AAGTTGATTGGTCAG[A/T]TATTCTAAGTCAAGG | 1130 |
rs553688515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235865135 | TCCTCAAACAAGCCC[A/G]GCACACAGGGCTTCT | 1130 |
rs553692545 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822706 | TAATTGCAGTTCCTC[C/T]TATCAAGTGATAGAG | 1130 |
rs553711490 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693068 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 1130 |
rs553713352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235881258 | TTTCAACAGGTTTGC[A/G]AGTTCTTCTGTGTGG | 1130 |
rs553716043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678142 | AAATAATTAAAGTTT[A/T]TTAAGAAGAAATACT | 1130 |
rs553716507 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235848060 | ATACAGACATTTCAT[C/T]CAACAACTGCAGAAT | 1130 |
rs553747296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744547 | ATATGTGATAATCAT[C/G]GTTCAATTTCAGAGT | 1130 |
rs553755980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235812306 | GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAT | 1130 |
rs553767207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871875 | CTCTCACGTCCTTGC[A/C]TTAAAAGATTTCTAC | 1130 |
rs553793041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235819938 | GGCGTGAGCCACCGC[A/G]CCCAGCCAATACTTA | 1130 |
rs553796627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754116 | TCTAGGTGAGGGATT[C/T]ACTCCTCTCCCAGAT | 1130 |
rs553797957 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235668321 | TACAAGAAAATAGGA[A/G]GATGAACTCTAGTCT | 1130 |
rs553810570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745275 | GTGTATTTCTTTGAA[C/T]AGCTTTTTTTAGTGG | 1130 |
rs553811496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713121 | TTCTGTCACTTGTAT[C/T]ACTTTCTCATCTATT | 1130 |
rs553825171 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235774835 | AACTGAAATACAAAA[C/T]TATTATTGGAAGACT | 1130 |
rs553877436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862575 | CCAAGATGGGCAGAT[C/G]ACTTGAGGTCAGCAG | 1130 |
rs553885689 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235839822 | AAAATAAAATAAAAT[A/G]AAATAAAATAAAATA | 1130 |
rs553894879 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235749233 | ATACAAAGCCAATAT[A/G]CTTTTGAAGATACTT | 1130 |
rs553955331 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235877593 | GTATTTTTAGTAGAC[A/T]TGAGGTTTCTCCATG | 1130 |
rs553979625 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672845 | TTAAATTCCACTACT[C/G]ACCTCCCAACATTTG | 1130 |
rs554001321 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235789274 | CATGATTTAAAAAAA[A/T]ATATCATATTACAAA | 1130 |
rs554026727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714793 | TATAATAAACCTCAA[C/T]AATGTACTTGCCTTT | 1130 |
rs554028804 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763442 | TGGCAAATCAGTCAC[C/T]AGGTTCTACTGACTT | 1130 |
rs554062280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827058 | AAAGTTTATTTACTT[A/C]TTTATATTAAATGTC | 1130 |
rs554073540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235712254 | TAATTCTATTTGAGG[C/T]CTATCATAATTAATT | 1130 |
rs554073657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854842 | CCTCCTACTTGATCA[C/T]ACTGTCTGGTCTATT | 1130 |
rs554084193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721684 | AAACCACAGAGAATA[A/G]AACATCCTAAACCTG | 1130 |
rs554095765 | snp | A/G | 4.98153e-05 | 0.00499051 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809771 | AGTTAAATTTTTCCT[A/G]AGATTTTCTGGCATC | 1130 |
rs554121356 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235665325 | ATCTATAAGAAGTGA[C/G]TTGGCCAGGCGTGGT | 1130 |
rs554136375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751519 | TTTTAAATTCTTGTT[A/C]AAAGCAATTTTAAAG | 1130 |
rs554153334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831206 | AGACATGTATTGCCT[C/T]ACCTCCCTTCACCCG | 1130 |
rs554161738 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235835592 | CAGTTTCATTTTATC[A/C]AAGATCATAATTCTA | 1130 |
rs554164175 | snp | C/T | 3.38685e-05 | 0.00411498 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752160 | AGCAATTTATATTCA[C/T]TCATGGGAATGCTAA | 1130 |
rs554170944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797367 | GCAAGTGATCAAGGT[C/T]AACATCAACAATTAT | 1130 |
rs554198913 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235837589 | CTGAGATTGAGCCAC[C/T]GCATACCAGCCTGGG | 1130 |
rs554218242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235780069 | TATAAGCAGAATTAG[C/T]AATACTTTGAAAGCA | 1130 |
rs554220634 | snp | A/G | | | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235865202 | TTCCCTCAGAGAGGT[A/G]CATGGATTACCCCTC | 1130 |
rs554227434 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235790308 | GGTTTCAATTCCTTT[A/C]CATCACTTACCAGCT | 1130 |
rs554253230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727004 | CCCTGTGGTAATTGC[C/T]ATATAAATGAGAAAA | 1130 |
rs554287370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692732 | AAGATACCACAAAAA[C/T]GTTTACATGGGCCAG | 1130 |
rs554291989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735592 | GACAATAATGTTGCC[A/C]ACAAGTTAAACATAT | 1130 |
rs554292250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824580 | GGCATGGTGGTATGG[C/T]AGAAATATTCAACTT | 1130 |
rs554298316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695924 | ACAGGCTTGAGCCAC[C/T]GCACCCAGCCTACTG | 1130 |
rs554302281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235683576 | TCAACAGAAACTTAC[A/G]GTGCTCAAAGTTAGA | 1130 |
rs554302951 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235798029 | ATGAAAAGAGGTTCA[A/G]CATCACTAATCATTA | 1130 |
rs554309926 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235735590 | TAGACAATAATGTTG[A/C]CAACAAGTTAAACAT | 1130 |
rs554315996 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235694113 | TTCCTGGGTTCAGGT[C/G]ATTCTCGTGCCTCAG | 1130 |
rs554334441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798020 | AATAAGTACATGAAA[A/G]GAGGTTCAACATCAC | 1130 |
rs554345380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802331 | CTCATTTTAAGTCCA[A/G]AGACAAGGGAGGAAA | 1130 |
rs554393796 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662035 | AAAATTCTTCCTGCA[A/G]ATTAGATCAAATGCC | 1130 |
rs554407289 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810360 | GCATCTCTTACAGAA[G/T]AGCGATGGGTAATTT | 1130 |
rs554411331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235760015 | GTCTTCTTAACAAAA[C/T]ACAGTATTGACTGAA | 1130 |
rs554437967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704300 | CTGGGTAGAATAGTA[A/G]TTCTGTTTCTAGCTC | 1130 |
rs554444715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766426 | TACCATAACAACTCA[C/T]TAAATTGAGTTATTT | 1130 |
rs554470194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795470 | CCTGGATCAAGAAAG[A/G]GATGCCTTTTTTCTC | 1130 |
rs554498622 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739962 | GTGGGAAAGGGAAGA[C/T]GGTATGAGAAAAAGT | 1130 |
rs554505943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767368 | TTTAAGAAGGGAACA[C/T]TGAGTCTACAGAAGA | 1130 |
rs554507185 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235759975 | ACTTTTTATTAATAT[C/T]TTCCCAAAACATATG | 1130 |
rs554536907 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235672918 | CTTCCACCCTTTACT[C/T]ACTCCCTCAAGACTC | 1130 |
rs554572161 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235757013 | AGATTTAAAAGACAT[A/G]TTGATATGAACCAAC | 1130 |
rs554582736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772660 | TTAATTTGTACTTAC[A/G]ATGAAGCCTTGCCCT | 1130 |
rs554649630 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885064 | CCCAACTAGCACTTT[C/G]CCAAGTTGCTCTTTT | 1130 |
rs554653615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877136 | GTCTGTGGGATCCCT[A/G]GTTGAAGTCAGCACT | 1130 |
rs554667201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780569 | CAAGTGTTATTTTCA[C/G]TGTATCATAAACATT | 1130 |
rs554674473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864088 | CCCCCTTATCCCTGA[C/T]GTTTCCTTTTAGCAA | 1130 |
rs554687551 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235843276 | AAATATTTTAATAGA[C/T]ATTTATTAATATGCT | 1130 |
rs554688237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235877692 | ATTACAAGCGTGAGC[C/T]ACCGCGCCTGGCCGG | 1130 |
rs554689255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727959 | TCAGACCAATCTATA[C/T]ATAGAGTGACAAAGA | 1130 |
rs554699166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235777858 | AAGGATAGTTTCCAT[C/T]AGTGTGTGGCTCCCT | 1130 |
rs554715815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845498 | GCTGGCCAGAACTCC[A/G]GGGAGGGTGCAAATC | 1130 |
rs554716650 | in-del | -/TTTT | 0.465368 | 0.126951 | intron-variant | LYST | GRCh38.p7 | 1:235856941 | CACAGGATATACTGA[-/TTTT]TTTTTTTTTTTTTTT | 1130 |
rs554748468 | snp | C/T | 1.66029e-05 | 0.00288117 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808969 | GATCCAAAATAAGTT[C/T]GTTAAGGATATTCAA | 1130 |
rs554752993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837227 | AACACAGGAGACTGA[C/G]AAGGAACAGCAAGTG | 1130 |
rs554756352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235740827 | GTAAATATCTAAAAA[C/T]GGAGTAACATGGTGA | 1130 |
rs554772241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852924 | ATACAATTTTTGACA[C/G]ACTACTCACAACCAA | 1130 |
rs554786888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235882800 | GCCTTGTGTAAAAAC[A/G]TCCCACATGAGTCCA | 1130 |
rs554792563 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235750444 | AGAAGTAGCTTAACA[C/T]GGGTGAAAGAAAGAT | 1130 |
rs554819530 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235772040 | CCAGCCTGGGCAATA[A/C/T]AGTGAGACTTCATCT | 1130 |
rs554820833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785765 | CCATGCTACATTACA[A/G]TTTCGAATTCTCTAT | 1130 |
rs554821964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779119 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 1130 |
rs554835159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836322 | CCATCATGTATTATA[A/G]TGAGGTGGAGACAGA | 1130 |
rs554840569 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235735990 | TCTTGATATAACTTT[A/G]AAAATATTTCAGTTT | 1130 |
rs554841002 | snp | A/T | 0.000329881 | 0.0128387 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733525 | GTGTCAGCTGCTGAA[A/T]AAGTTCCTGCCAATG | 1130 |
rs554865330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696713 | ATCTCGACATCCTTG[C/T]TGTGTTTGTTGCTTA | 1130 |
rs554899697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235850855 | TGCAAGAATGGCCAT[A/G]ATCAAAAAATCAAAA | 1130 |
rs554912555 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235688520 | GCTTTCATTGAACAC[A/G]GTGGAGAATTCAGAA | 1130 |
rs554917087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708739 | GCTTTACCAGGGGTA[G/T]ATTCTTGGATGTTTG | 1130 |
rs554935750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814974 | TCCTCACATACACTG[C/T]TTCTGCAATTCTCCA | 1130 |
rs554942509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748271 | CCTAATGCTGACTAC[C/T]TCTACCTTCATGCAT | 1130 |
rs554976405 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235797118 | ATGACACAAAATAAA[C/T]GACTCGAGAAATGAA | 1130 |
rs554986679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764024 | GAATTACCACTATTT[A/G]TCCCTAGGTCCCTCC | 1130 |
rs554987668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682127 | ATAGCCTGAGCAACA[C/T]AGTGGGAGCCCGTCT | 1130 |
rs554989508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823339 | AGAACTAGGTTTGTG[C/T]GTGAACAGAAACTGC | 1130 |
rs555005507 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235716503 | AATTTATGCCAAAAT[A/C]AGTGTATTCTTTTTC | 1130 |
rs555029038 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235699823 | TTTGCATTTCTCTAA[C/T]GATCAGTGATCCTGA | 1130 |
rs555051035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882180 | ACAAAGGAGATGGCT[G/T]TGTCTTGAAAAAAGA | 1130 |
rs555110690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714834 | GCAATAATGTACATA[A/G]GCTCCAAAGGTAACT | 1130 |
rs555130612 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235861126 | CATTTCTAATATGTG[C/T]AGTACTCTACCCTAT | 1130 |
rs555147370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714348 | CAAGAGAGAGAGAGA[A/G]AGGGAACAGGCCAAC | 1130 |
rs555204874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844874 | TTAAGCAAGAAAATA[C/T]CTGTTAATCTAAGCT | 1130 |
rs555206501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755308 | GCAGGAGAATCGCTT[A/G]AACCTGGGAGGCGGA | 1130 |
rs555212096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829524 | ATTGTAGAGTTTTAC[A/G]ATCACAAAATAATTA | 1130 |
rs555223237 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829727 | GCAAAACCATATGGT[C/T]ATACCATACTTTAAG | 1130 |
rs555227861 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235875091 | TATATTTTGTTCCCT[C/T]CATTCCTAGAATAGA | 1130 |
rs555236973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857957 | ACTTTTAAGATTACA[C/T]TATAGCTATATTTAT | 1130 |
rs555241048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689517 | TGTGGAATGGAGAGA[A/T]GGTGGTCAAAGGGTA | 1130 |
rs555264697 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867809 | ATCGTTCGGTAGTTT[C/T]CAAGTTCTGCCAAAC | 1130 |
rs555266207 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841092 | GGCCAGTGACTAACT[G/T]CTTTACAGTGACTAC | 1130 |
rs555337472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762933 | AAAGCAGATCATTAA[A/G]TTCAAATTTTGACAA | 1130 |
rs555350987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235829969 | TAGTTATCTCACTGA[C/T]ATTACGATAAAAAGC | 1130 |
rs555355339 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235694123 | CAGGTGATTCTCGTG[C/T]CTCAGCCTCCCCAGC | 1130 |
rs555358229 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235879342 | AGATGTCTGAAAGCA[A/G]GACAAATCTTTGGCC | 1130 |
rs555366249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707583 | AGCTGAGATCACGCC[A/G]CTGCACTCCAGCCTG | 1130 |
rs555391601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740426 | AATTCCCTTTCTCAC[C/T]GTCCCCCTTCCACAG | 1130 |
rs555434309 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235785079 | TTATTGAGGCTGGAC[A/C]GCTGTAAGCAATCAA | 1130 |
rs555436515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844186 | AGAGTTTAATATATA[C/T]TGATAGATTGATTAG | 1130 |
rs555451397 | snp | A/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713018 | ACTTGTTGAAATTTG[A/G]ACACATCTTTTCATT | 1130 |
rs555477803 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235673833 | AAAGTCAAGGATTTA[A/C]AACAAACTTTAGCCA | 1130 |
rs555479456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722532 | ACTCTGTTGCCCAGG[C/G]TGGAGTGTAATGGCG | 1130 |
rs555479991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688742 | TGTAACCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 1130 |
rs555516686 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235694618 | GCAATTCACAGCTTT[C/T]TGTTTTGCTGAGTAA | 1130 |
rs555524117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235820512 | GTAGCTGGGACTACA[A/G]GCACGTGCCACCACA | 1130 |
rs555525346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235880490 | TAAACACATCTTTGC[C/T]ACACCTAATATGTAC | 1130 |
rs555534829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835577 | ACTTGAATATCTATG[C/T]AGTTTCATTTTATCC | 1130 |
rs555537160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804915 | GGTAAAGAATGGCAA[G/T]AAATGAAGCTAAGCG | 1130 |
rs555541661 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235680683 | GGCCCACTGCAACCT[C/T]CACCTCCTGGGTTCA | 1130 |
rs555556165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769355 | ATGAAGCTAGAATGG[A/T]AGCCAGATCATATAA | 1130 |
rs555562006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235872522 | GCATCTGTGTGCAGC[A/G]TTCCTTCTTCCCGGA | 1130 |
rs555585727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665779 | TTAATTTTTTCTTTT[A/C]AAAGATTACAGAGTA | 1130 |
rs555604905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687745 | ACTTCACTAAGCAGA[C/T]GGAGACCCCCAGCTG | 1130 |
rs555616788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693262 | TGGAGCTTGCAGTGA[A/G]CCAAGATGTGTCACT | 1130 |
rs555619657 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235731661 | CCTCCCGGGCTCAAG[C/T]GATTCTCCTGCCTCA | 1130 |
rs555627917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699803 | GTATCTCCTTGTGGT[G/T]TTGATTTGCATTTCT | 1130 |
rs555636566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762612 | GTGTCTCTTGTTAGA[C/T]TGAATGAGGTTGTAC | 1130 |
rs555638752 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235677073 | CCAGCCCTGTGCTTT[G/T]GGTTGGAGCAAGCTC | 1130 |
rs555648148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798306 | TATGGACTTCAGTTA[A/T]TAATAACATATCAAT | 1130 |
rs555648376 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235684450 | GCAGGGTTTAGAATC[A/G]ATTTGTAGGGGAAGT | 1130 |
rs555655578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692945 | AGGATCACTTGAGTC[C/T]GGGAGGTGGAGGGTG | 1130 |
rs555663139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707172 | ATCCAGGCAGGCCCA[C/T]CTACCTTGGAGAGGA | 1130 |
rs555708285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235730724 | ACCTTGTCCTCCCTT[A/G]AGCCTTTCCTGTTTA | 1130 |
rs555747182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738745 | TCAAAGGCTACACAT[C/T]CTGGGCCATTGGACT | 1130 |
rs555766572 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771184 | AAAACCAGCAGACAA[C/G]GCAGCCAAAGTATGA | 1130 |
rs555793172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663733 | ACAGTCTCTATGATT[C/T]CAGAGACACACTACA | 1130 |
rs555804802 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729544 | TTTAAATAATCTAAG[A/T]ATCAAATAAGGCAGG | 1130 |
rs555857160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672396 | AGGAACCAGCAAAAG[A/T]CTGAGAAGGACCCAC | 1130 |
rs555877321 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235776732 | CCCTTAGTTTTTTCC[C/T]ATGCATTGGAAACAT | 1130 |
rs555881649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235881061 | AGGAAATTAAGTGAC[C/T]TGCTGTACGTGATAT | 1130 |
rs555893432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780800 | CTAATTCATAACTAT[A/G]CATTACAATAAATAT | 1130 |
rs555921124 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813609 | GTCTTACCCTTTCTG[A/G]AGGATATGGTCCAAG | 1130 |
rs555954983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235856996 | TGTCGCCCAGGCTGG[A/G]ATGCAGTGGTGCGAT | 1130 |
rs555983021 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235810789 | CAAAACAGAGGCACA[C/T]CTATACTTACTCTAA | 1130 |
rs555985693 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | LYST | GRCh38.p7 | 1:235745488 | TGGAAATGTAAAACT[A/C]CAGCCACTCTGGAAA | 1130 |
rs555989332 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235742372 | AGGTAGGAGAATCGC[C/T]TGAACCTGGGAGGTG | 1130 |
rs555991484 | snp | A/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868733 | TGCAGCTTCACTCTT[A/T]TTCCCTGACTGGAGT | 1130 |
rs555996031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753948 | AATAAGGAGACACAC[A/G]TTTCTCTCTATTCTA | 1130 |
rs555996588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235760338 | GGTGCTCAAAAAATG[A/G]TAGTACTTGTTGTTA | 1130 |
rs556010943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235704763 | TAAGTTAGATCCCAC[C/T]TGTCAATTGTTGCTC | 1130 |
rs556019493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791249 | ATCGCGCCATTGCAC[C/T]CTAGCCTGGGCAACA | 1130 |
rs556032723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753346 | ATGATAGCAACTATG[C/G]GTCATCTTGCTAACT | 1130 |
rs556042098 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235686895 | ACTTCATAAAGGCTT[C/T]CTTCCCCTCATTGAC | 1130 |
rs556047374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746072 | TTATTCCTTAACTGC[A/T]TGTGAATCTACAACG | 1130 |
rs556052055 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739101 | GCAGTGATGTTAAGA[C/G/T]GGATTGGGAAAAACA | 1130 |
rs556056126 | snp | C/G/T | 3.53308e-05 | 0.00420291 | intron-variant | LYST | GRCh38.p7 | 1:235781877 | AAAGGAAAAAAATCT[C/G/T]ACTCTGTCGCCCAGG | 1130 |
rs556061907 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704065 | TCCAGCTCCATACAC[A/G]TTCCAACAAAGGACA | 1130 |
rs556062616 | snp | A/C | 0.000531358 | 0.016291 | intron-variant | LYST | GRCh38.p7 | 1:235677209 | AGAAAAAAGACATGA[A/C]TTTGTATATGATCAT | 1130 |
rs556098939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235736848 | TTGTATCTTCAACAG[A/G]AAAAAAAAGTCAGTT | 1130 |
rs556121452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684980 | GAACCTCATCACTGG[C/T]CTCAATCTTTTCCTG | 1130 |
rs556136315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751456 | ACAATAATGTTTTGA[C/T]ATAAATTTTTAAATT | 1130 |
rs556151782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878505 | CGGCCGCCCTGCTTC[C/T]GCCATTGTGGTTCCT | 1130 |
rs556163659 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813848 | AAAGGATTTAACGAC[A/G]AATCAAGTTTGAGTT | 1130 |
rs556163847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235721628 | GGATAATGAGAGAGT[G/T]AACTTAATGAGGAAA | 1130 |
rs556167050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235871807 | AGAATCTGCTCTCAG[G/T]GTCTGGGACAAGATC | 1130 |
rs556173059 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759246 | CCAACTGTTTATGAT[C/G]TGCTTTGACCACTGG | 1130 |
rs556174715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750701 | TATTATTTGATGACA[C/T]TCTTCCTTATTTAAT | 1130 |
rs556200563 | snp | A/C | 0.000477779 | 0.0154487 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720669 | AACTTACCTGTATAT[A/C]AACAGATCATTGAGG | 1130 |
rs556229482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825423 | CACAGATGACATCAT[C/T]ATTTACATACAAAAT | 1130 |
rs556235169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235768147 | ACTGTTGCTGAATAT[C/T]CTGCTGTAATTTCAA | 1130 |
rs556248490 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885387 | ACTATTCTGTAGTGT[A/G]TGTATTTGCTCAGAA | 1130 |
rs556249572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713056 | TGCCACAAACACATC[A/G]CAGCATCAGGTTTCT | 1130 |
rs556300408 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235669371 | AAACCCTAACTTTCC[A/G]GGCCTAAAGAACAAA | 1130 |
rs556300666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235737441 | GAAGAAATGACAACC[C/T]AGGAGAAATAAACAT | 1130 |
rs556335732 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235743905 | TATGATTTTGAAAAC[A/G]TATAATACAGTCAAC | 1130 |
rs556369376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831276 | GCAGTGCACATATGA[C/T]TATGCCTCTTGCCAA | 1130 |
rs556374578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235788573 | TAGCTGTTAGAATGT[A/G]TATATTTTTAAATGA | 1130 |
rs556383058 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235728651 | GCTGTTGCTAACCCA[C/T]GTCCCTACATCGTGT | 1130 |
rs556411189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678021 | AACTATCCTTCATTG[A/G]TAGACACTTAAAATT | 1130 |
rs556412449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235758713 | TTTCCTTAATAACTA[C/T]AAGGAATTAAACCAC | 1130 |
rs556422812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235861660 | TACATATATATGTTT[C/T]GTTTGTTTGTTCTGT | 1130 |
rs556426768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879687 | TAAAACAGAGAAATA[C/T]GGAACTATAAACTGA | 1130 |
rs556428133 | in-del | -/A | 0.492139 | 0.0621989 | intron-variant | LYST | GRCh38.p7 | 1:235663084 | AAATGTAAGGCTGTA[-/A]AAAAAAAAAAATTCC | 1130 |
rs556434680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692200 | TAGCCAAGTGTGGTG[G/T]CACATGCCTGTAGTC | 1130 |
rs556460453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862622 | GCAACACGGTGAAAC[C/T]CCATGTCTACTAAAA | 1130 |
rs556461816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823927 | CTGTCCTTTCATCTC[C/T]GCATCTAGCAGAGGT | 1130 |
rs556474319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235703422 | TTCAAAGCTCTTAAA[C/T]GTAAAGGGTATTATT | 1130 |
rs556498720 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693805 | CATGTTCTGAGACAC[C/T]TTTTCTTTTAAAAAT | 1130 |
rs556502349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235816320 | ATGCCATGTGCCTGT[A/G]GTCCCAGCTACTCGG | 1130 |
rs556540615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235729001 | TCTAAGAAGCTCCCA[C/T]GAGATGCTGATGCTA | 1130 |
rs556548776 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235696906 | TTTCAAATAGCACTG[C/T]ATTTAACTCTCTGTT | 1130 |
rs556553397 | in-del | -/AAC | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865845 | TCAATCTGTTAAACA[-/AAC]AATAGGAAAATGCAA | 1130 |
rs556568529 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235730541 | TATATATGTACCCAT[A/G]TATGTGTATATATAT | 1130 |
rs556587814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813460 | GCCTTCATGCAGTTA[A/C]ATGAAAAACTCAGAG | 1130 |
rs556594476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696297 | GGGTGGAAGGCTATA[C/T]ATGGCTCCCAAAGAG | 1130 |
rs556606511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710473 | CAAACTCAATCTTTC[C/G]CAACTTTCAGGTGTT | 1130 |
rs556613423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797204 | GTAGCAAAAAAGGAG[A/C]ACAACCCAAATGTCC | 1130 |
rs556645256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690409 | AATTTAGTTATACTA[C/T]AAGCTTTGCCATGAT | 1130 |
rs556651947 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235847785 | GCAACAGCAGTTAAA[A/G]GAGACAAAGAGGGAC | 1130 |
rs556658969 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235755233 | TCTCTACTAAAGATA[-/C]AAAAAACTAGCCGGG | 1130 |
rs556668003 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235737081 | CTAATTGGTTGAAGT[C/T]GGCAGCCTGACCAAA | 1130 |
rs556682168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726122 | TTTCTTTTTTAAATC[A/T]GTTTTTTTCCTTTTA | 1130 |
rs556698325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235741918 | ACATACAATGGAATA[C/T]TATTCATCCTTAAAG | 1130 |
rs556704415 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862036 | GGGACAACAGATCAA[A/T]TCAAAATGGAGTCAC | 1130 |
rs556705609 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235766864 | GATTAGGACAGAAAA[C/T]TTTTGATGGACAAAA | 1130 |
rs556726229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839114 | ACAGGCGTGAGCCAC[G/T]GCACCTGGCCTCATT | 1130 |
rs556731522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807546 | AAATGACTGTAAGGC[A/G]TTGATTTAACATCAA | 1130 |
rs556747358 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884282 | GCCCGCCACTACGCC[C/T]GGCTAATTTTTTTGT | 1130 |
rs556768346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235808224 | CATACATAAACAAAT[A/G]GTTAAAACAAATCTG | 1130 |
rs556791141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235766386 | TTCTGTTGGTTTACT[A/G]CTCTAGTCTGATCAT | 1130 |
rs556812087 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235870470 | GCTGTCCATAAATCT[C/T]CCACCGTGTGGCTGC | 1130 |
rs556822096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676340 | GCTCCTGCACTAGGC[C/T]CTAACATACCAGATC | 1130 |
rs556829458 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235810781 | TAAAACAACAAAACA[A/G]AGGCACACCTATACT | 1130 |
rs556835802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235695759 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 1130 |
rs556835804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845002 | GGAGGCAGGACTAGA[C/T]TGCAGCTCTGGACAG | 1130 |
rs556850546 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235879477 | GTTAACTGGCTGTCT[-/A]AACCAGACACCTGAC | 1130 |
rs556872364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235701661 | CAATCAAGTGACAGA[C/T]TGTAGTTAAAAATAG | 1130 |
rs556876889 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864753 | CCTGGGCAACAATGG[C/T]GAAACCCCATCTTTA | 1130 |
rs556885846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702561 | GAGCTCCCCAAAGCA[C/T]TCTCTCATATCGCTA | 1130 |
rs556909273 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235752277 | ATTCCTGTTCGACCA[A/G]CTTGCACTCATTCAT | 1130 |
rs556909331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792441 | TGCCTCAGCCTCTGG[A/G]GTAGCTGGCATTACA | 1130 |
rs556924327 | snp | A/C | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830360 | GGACCACTGCATTGC[A/C]AAGCCGGTTGACATC | 1130 |
rs556962265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673916 | CGCTCACACCTTAAA[C/T]AAAAGCGATTGTTGC | 1130 |
rs556970553 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235787739 | ATAAATGTCTAAGTA[C/T]TGGAGGTCTAATCTA | 1130 |
rs556974062 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235852267 | AAAATGAATTCAGAG[A/T]TCCAACTTGAATTGC | 1130 |
rs556986034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876119 | CCCAGCTACTCAGGA[A/G]GCTGAGGTGAGAGGA | 1130 |
rs556993119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814836 | TAGAAAACCCTTCAC[A/G]GCAATGATTCCTGTT | 1130 |
rs557004269 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235772823 | AGCCTTCAGCTGATC[C/G]AGATAAGCCCATATG | 1130 |
rs557006648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802235 | ACTAGCAGTACTGGG[A/G]CACTCACAAGGTCAG | 1130 |
rs557035134 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687940 | CCCCCTTGCACTACA[A/G]GTGTGTTCACGTCTC | 1130 |
rs557059751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235735500 | CTAAACCAAACGTTC[A/G]TTCACGGTTTTTTAA | 1130 |
rs557081321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675546 | GCTAGTTTTTCTTTA[C/T]GGCACCAAGCACTTG | 1130 |
rs557089239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235784370 | CAGAGTGATATGTGA[A/G]TCAAGTGACCATGCT | 1130 |
rs557091200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793302 | GCGATATGTCTGGTT[A/C]ATCCAAATTGAAGTG | 1130 |
rs557098229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822626 | TAGAGGGGAGTGAGT[A/G]TAGGAGGAATAATAA | 1130 |
rs557113961 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235779333 | ATATGACCTATATAC[C/T]GTTCAGGAAAAATAA | 1130 |
rs557114270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787173 | TGTAACTGAGATTGA[A/G]ATGCATTTTCTCAAA | 1130 |
rs557118639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874940 | TGTTCCAAGCCCAGG[C/T]TCCTCCTCCAACCAG | 1130 |
rs557121638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235709936 | GGTTCTTCTGTGATG[C/T]AAATGAGCTAATATC | 1130 |
rs557126948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667261 | AATCTTAGAATATTT[C/T]ACTAACTCTATCTTG | 1130 |
rs557171577 | in-del | -/TC | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235768081 | TTCTCTCACTACGTT[-/TC]TCTGTCTTGGAGTGC | 1130 |
rs557174026 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235825936 | CCAAACTTATTTTTA[C/T]AAAAGCCACAGTAAT | 1130 |
rs557174374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235741136 | TCCAAACAATCCTTA[A/C]ATAAAACACTTCAAG | 1130 |
rs557186301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771951 | TTTTTGGCCAGGCAT[G/T]GGGGGCTCACGCCTG | 1130 |
rs557187959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235757828 | CATGAATAAAACATG[C/T]CCATCATTGCAGAAA | 1130 |
rs557190313 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235734901 | CATAGGAAAACATTT[A/T]AAAAAAAGAATTTAG | 1130 |
rs557202520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716401 | TAACACTAGGGGATA[C/T]GAATAGCAGGTCCCT | 1130 |
rs557230467 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235801614 | CTGCTGTGCTCTTAA[C/T]AAAATGTTGATACAG | 1130 |
rs557234263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680804 | AGGTTTCCCCATGTT[G/T]GCCAGGCTGGTCTCG | 1130 |
rs557249616 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685063 | AGTATTTGCCACCCC[C/G]CAAAATCCCCATGCC | 1130 |
rs557251273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749541 | TGTGCCAGCAGTCCC[A/C]AGTTCTAGGATGCAG | 1130 |
rs557292258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235748173 | GAAATATAAAGTTCA[C/T]TTGTATGTGAATTAC | 1130 |
rs557359349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724861 | AAACAAGGGAAATGA[C/T]ATCCCCAGAAGTCAA | 1130 |
rs557362953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762414 | AAGTGAAGTTGTCCA[C/G]AATGATGGTTTTAGG | 1130 |
rs557364827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235754233 | TCTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 1130 |
rs557374283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771193 | AGACAAGGCAGCCAA[A/G]GTATGAAAACATGAT | 1130 |
rs557414361 | snp | A/C | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804550 | TCTGCTGAATAATTC[A/C]CGAGGGCAACTCGAA | 1130 |
rs557427656 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857932 | AAGTCATTGTTATTC[A/G]ATTTTATCCACTTTT | 1130 |
rs557432402 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867153 | ACCCGCGGGGCTGCA[C/G]CCGGGGCCCGGTCTG | 1130 |
rs557469360 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867726 | TTGGCATTTCAAGGG[A/C]CACCCTCCTCACCTC | 1130 |
rs557502034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763352 | GCCCTAAATTTACTC[C/T]TTCTGTTTTGTTCTT | 1130 |
rs557509451 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235722546 | GCTGGAGTGTAATGG[C/T]GTGATCTTGGCTCGC | 1130 |
rs557552832 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235730591 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 1130 |
rs557560870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235843948 | TCTCAATTCAATAGT[A/G]TTAGAGAAGTTGCCA | 1130 |
rs557562700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834965 | TTTCGCCCAGGCTTG[A/C]GTGCAGTGGCGCGAT | 1130 |
rs557570844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732014 | AAATAAGAGAAAAAA[A/G]TACCCTTATTCATAC | 1130 |
rs557583971 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235678980 | ATATTAGGTACAGCT[A/G]TCTATCTTAGCTGCT | 1130 |
rs557599398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235835458 | TGGTCAGCTAGATCC[A/G]TCTGTTTCTCTTATC | 1130 |
rs557604741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850709 | CCCATCAAAAAGTGG[C/G]CTAAGGACATGAATA | 1130 |
rs557608274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872926 | GTCTCAAAAAGCAAA[A/C]AGAAAGTTGGGAAGA | 1130 |
rs557608360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865339 | CTGCCCTCCCTCTTC[C/T]GTGCTTTTTCTCTGT | 1130 |
rs557615424 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235777761 | CTAAACTAGATCTTT[A/C]TACTGGAATAAAATT | 1130 |
rs557672060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721740 | TGTTAGCGCTAAGGT[C/T]CACGGAAGGGGATTT | 1130 |
rs557680943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828936 | TTGGCTGGGTGCAGT[A/G]GCTCACACCTGTAAT | 1130 |
rs557691382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874075 | GGTCAAGGTAAGGAA[C/G]AGGTAAAAATATATA | 1130 |
rs557704147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840948 | ACTCTCTGAATACTG[C/G]CTTGGTTAACTGGAT | 1130 |
rs557738030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235769926 | AACATCTAAGAAATT[C/T]AGTAATTGTACTTTT | 1130 |
rs557758968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706997 | TTGTTATAAACGCTT[C/G]TAGATTTGCTACAGT | 1130 |
rs557764255 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806297 | GCAAGACAAGGCTCT[C/T]GAGAGATATACATGG | 1130 |
rs557776210 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704761 | CTTAAGTTAGATCCC[A/G]CTTGTCAATTGTTGC | 1130 |
rs557833626 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235694054 | TCGCTCTGTCACCCA[G/T]GCTGAAGTGCCGTGG | 1130 |
rs557872136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729815 | CATGAAAATATTAGC[A/T]CCTTTTTAGCATTCT | 1130 |
rs557927457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776335 | GCAAAATTAATCAAC[A/G]ATGCTTCCATTAAAG | 1130 |
rs557954825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853828 | GAAGTCACACTAAAA[C/T]GCACCAAACTTAAGC | 1130 |
rs557981388 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235776103 | ATTTTGAAACTATAC[A/G]ATGGTACAAAATATC | 1130 |
rs557991257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235747671 | ACGTGCAGCTGATGA[C/T]TGTAATTCAGCGGTA | 1130 |
rs558004061 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235883065 | ACAGCACTGCCAGAA[A/G]TTCATCCACCAGTCA | 1130 |
rs558013095 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235679974 | TTGTCAGATCTTCAA[A/T]GCTTTTAAGGCTCTC | 1130 |
rs558015862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826538 | AAAGCTACATTTAGA[G/T]GCTAAAAGTCACAAC | 1130 |
rs558027848 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235698485 | TGTGGGAACAGAGAC[C/G]TTAGGGTCAGGCATT | 1130 |
rs558029632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848139 | TGACAGGCAACAAAA[C/T]GAGTCTCAATAGATT | 1130 |
rs558030274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854938 | ACTCCAATTCATAGG[C/G]AAGAAGATCCCAACT | 1130 |
rs558033435 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670636 | GTGACCAAGTAATTC[G/T]GTGCACAGACCAAGG | 1130 |
rs558037523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820473 | TGCCCAGGCTCAGGC[A/G]ATCCTCCCGCCCCAG | 1130 |
rs558039464 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235812380 | GGCATGGTGGTGCAC[C/G]ACTGTAATCCCATCT | 1130 |
rs558052259 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235721483 | GGGGTATTGGTTCTT[C/T]TAAAGCAATTAAATA | 1130 |
rs558063297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752396 | CCTGTCAGAAATACA[C/T]AGTTTTACAGAGAAC | 1130 |
rs558066653 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235705390 | TTCAGATACTTTTTT[A/T]TAAAAAAAAAATTGA | 1130 |
rs558079989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714225 | TTTAGTACAAAACTG[A/T]CCTATTTATTTTTTG | 1130 |
rs558092317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692792 | CTGGGAGGCCAAGGC[A/G]GGTGAATCATTTGAG | 1130 |
rs558094387 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235846684 | TAAAGAAAAAAAACA[A/G]TAAAAAATTCAGGAA | 1130 |
rs558141704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790404 | GTTAAGATTAAAAAT[A/G]TATATAGAACCAGCT | 1130 |
rs558148476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235817803 | TAGTCTGTACACCAA[A/G]CCCCATGACATGCAA | 1130 |
rs558151314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745350 | AGCCAATATGGAAAT[A/G]CAAATTAAAACCACA | 1130 |
rs558151506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235873457 | ATACACAATATACAA[C/T]GTAGGAAATGGAAGT | 1130 |
rs558162561 | snp | A/C/T | 0.000148588 | 0.00861822 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806698 | TTTAGAGAATGACTT[A/C/T]GAATACCATTTAAGC | 1130 |
rs558162616 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235842391 | CCACAGTGTGGCCCT[A/G]CAAGCAGATGTCTAA | 1130 |
rs558183344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818692 | CGGTAGAGTCCTCCT[A/C]ATCTGAGTCTTTATC | 1130 |
rs558201845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797464 | TCCTCTCAAAAGTCC[A/G]TACCCCTAGCATAAT | 1130 |
rs558233192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235880461 | TCATCATTTGACACC[A/G]TCATAACAGTGACTA | 1130 |
rs558235186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686260 | TGGTCCCAGCTACTC[C/G]AGAGGCTGAGGCACG | 1130 |
rs558239624 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669287 | TCCTGGTGAGGCAGG[A/G]GAATAGGGTCTGGAG | 1130 |
rs558246945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824630 | AAAGAATGTTTTTGA[C/T]ATTTAAAAAGAGTAT | 1130 |
rs558270366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235783150 | ATAAAATTTGTAAGA[C/T]GAAGACAGGATAAGC | 1130 |
rs558272674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679135 | CTGCCTGTTTAGCTA[A/G]GGCGTGTGACCTTCA | 1130 |
rs558282135 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235864548 | TAGGGCAACAGTTCC[A/G]GATTGGTATCCCAGC | 1130 |
rs558289683 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235796176 | TATGGAGAGGAGAAA[A/C]TTATTTTTTAAAATA | 1130 |
rs558291667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787543 | TACCATAAGTTACTT[A/G]GTTATTCTATCATTA | 1130 |
rs558303110 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235782490 | CAATGGGGAATTCTT[C/G]AACAATTTTCTTGGG | 1130 |
rs558314333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774285 | TATTAGGCTTTAAAA[C/T]GTTTTCAAAAAAGTA | 1130 |
rs558342180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235712384 | CTTGAGATCATATTA[A/C]ATTTTTCATCTGTAT | 1130 |
rs558363716 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813533 | TAAGGAGAGAAAGAC[G/T]TATTAGTGAATGTAA | 1130 |
rs558387446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235669727 | CCAGGCCCTTGAGCC[A/G]CTGCTTGGGTCCACT | 1130 |
rs558395431 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235804881 | CTTAGTTCATCTTAT[G/T]TGGTTTTCATTGCAG | 1130 |
rs558420892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235760152 | GTGTGGGCTTTGCAA[C/T]TAGATATAATTGGAT | 1130 |
rs558421101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684809 | TTTTTGTTTTTTTTT[G/T]GTAGAAATAAGGTCT | 1130 |
rs558422613 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235818350 | CAAACATACTTCTCA[C/G]TCTTCTCTCAGGGCA | 1130 |
rs558423918 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235798165 | CAAAAACAAGGAAAG[A/T]CTGAGAAACTGTTAC | 1130 |
rs558426428 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235691151 | TCTCGATCTCCTGAC[C/T]TTGTGATCCGCCCGC | 1130 |
rs558427778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235856040 | GAGCACAGAACAGAA[A/G]TAAGAAAGAAATATA | 1130 |
rs558450280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235788482 | CATGAGCCACCACAC[C/T]CAGCCGAGAATTAAT | 1130 |
rs558525345 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235702535 | TGAAACGATGAATTC[-/T]TTTTTCCTCTGAGCT | 1130 |
rs558535382 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885177 | GGTACTTTTATTCCC[A/G]TTTTACTGATAAGGA | 1130 |
rs558560148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780761 | AAGAAAATGATAAGG[A/G]ACCACATTAAAATCT | 1130 |
rs558568682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765716 | CTACTCAAAATCTTC[A/G]ATGTCTACATCAGAT | 1130 |
rs558571403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235781787 | ACAAGTAAAGGAACA[C/T]AGATGGATATTTTAG | 1130 |
rs558576917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670096 | TTGTAATTAGCAAAC[A/C]TCTATATGCCCAGAC | 1130 |
rs558583946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235681119 | ACCCACAGATAAGTC[A/G]CTTCCTCAGACTGGG | 1130 |
rs558607793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728005 | TCTTCCTTCTCTCTA[C/G]TTATACTGAATTGAT | 1130 |
rs558621436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831230 | TCACCCGCTTCAGGG[G/T]GAAGCCCTCCCCACA | 1130 |
rs558626131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870212 | AGTTGTTAAATCAAG[G/T]TTAGCCTAAAGCTGC | 1130 |
rs558627369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774770 | ACTAGAAGAGTATCT[C/T]AGTTTGATTAACTAT | 1130 |
rs558656979 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235767493 | TCTGCTACAACCATC[C/T]GCATTTCTTCTAAAC | 1130 |
rs558660953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870924 | TGCATGGGAACAGAA[A/G]TGGATTTGTGAAGTG | 1130 |
rs558664076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235720567 | TAATTCTTCTATTTT[A/G]TGCATGTTTGAAATT | 1130 |
rs558691816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766479 | TTAAAAATTCATTAA[A/C]ACAGATGGCAACTTA | 1130 |
rs558712530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743777 | AGGCTTAAAAAGCAA[C/T]GCTTCATGAGTTGAG | 1130 |
rs558750796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846787 | AGAAATTCAGAGCTC[A/G]AAGACAAGGTCTTCG | 1130 |
rs558761659 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736285 | TAATAAAGTGCTAAA[A/G]TATGTAAAATATTTC | 1130 |
rs558790474 | in-del | -/ATGTA | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739525 | GTACATTACCATATT[-/ATGTA]AAGAGATCTACATAT | 1130 |
rs558795573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235764754 | GTAATCTGCCTGCCC[C/T]GGCTTCCCAAAGTGC | 1130 |
rs558819327 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802987 | AACTAAAAGTTTAAA[A/G]CTACAACACTGAGAA | 1130 |
rs558820972 | snp | G/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827094 | ATAAGCTGGGCGCAG[G/T]GGCTCACACCTGTAA | 1130 |
rs558831220 | snp | A/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235690948 | TTGAGACAGAGTCTC[A/G/T]TTCTGTTGCCCAGGC | 1130 |
rs558864904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829995 | AAAGCATAGTATATA[C/T]GAAACCATTTAGTTC | 1130 |
rs558866831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235725876 | CAAATCCCCACATTC[C/T]GAAATGAAGAGGTAG | 1130 |
rs558892505 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235727700 | CAGAATTACTTAAGT[A/T]ATTCAATTATTTAAT | 1130 |
rs558896288 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660837 | GGAGGTTGCAGTGAG[C/T]TGAGATCGTGCCACT | 1130 |
rs558906831 | in-del | -/CTAT | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235754207 | CTGAGAATACATGAG[-/CTAT]CTTTTTTTCTTTTCT | 1130 |
rs558911113 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865624 | ACAATATGGATGACA[A/G]CAAAGAGCTATCAGA | 1130 |
rs558911687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881568 | CAAAGGGGAAGCAAT[A/G]CAAGTGTCCATTGAT | 1130 |
rs558917873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732863 | TTATTTGCTGAAAAT[A/G]TATTTCCAGGCTTTT | 1130 |
rs558918426 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235703202 | GGTTATAATTAGTTA[C/T]GTTTATAAAATTAGC | 1130 |
rs558932838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779217 | GCTTATAACTCCCAA[A/T]TTACTAAATCGGGCT | 1130 |
rs558948781 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235882266 | TAGGAAGTAAGGAGG[C/T]AATTCCAAGGTCATA | 1130 |
rs558954990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740467 | TGTCCTGAATTCTAT[C/T]GTCATATCTTGGTTT | 1130 |
rs558955840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668940 | AACTGGGGGCTAAGA[C/G]TAGCAAAAATTCTTT | 1130 |
rs558962288 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235710439 | TGGGCTGGGGATGGG[G/T]TGCATAAGGGCATTT | 1130 |
rs559003990 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235675469 | TCTTACGATCGGTCG[G/T]TCGGACGCAGGCAGC | 1130 |
rs559007374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803535 | AATTAAAAGATCTCA[C/G]AATGCAACTGTCTAC | 1130 |
rs559030762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717638 | GCAGCACCATAACTA[C/G]ACCAACAGCAAGATT | 1130 |
rs559050821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835759 | TGCCCTTAGCCCATT[A/G]TATATTTGCCTCTGT | 1130 |
rs559072495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850308 | CAAATCATGCTGGAA[C/T]AATCAGCTAGCCGCA | 1130 |
rs559120520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846116 | GGACCCTCACGGAGT[C/T]CACTGCACCCTCCAC | 1130 |
rs559125059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725101 | CTAGGAAGGGATTTG[C/T]TCCTAATGAAAGATT | 1130 |
rs559126362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702517 | CTGAGGGAGGTTACC[A/G]TCTGAAACGATGAAT | 1130 |
rs559137129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674713 | TAATATTGGCCAAAA[A/G]GGGCGGGGTCTGTGT | 1130 |
rs559143750 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235724474 | TGCACTCACAGTTTC[G/T]CTATTATTAAATCTT | 1130 |
rs559175741 | in-del | -/GGA | | | utr-variant-3-prime, cds-indel | LYST | GRCh38.p7 | 1:235662508 | CATGTGTGTGTGGTG[-/GGA]GGAGTATTTCATGGC | 1130 |
rs559177510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674003 | CTCCGACCCACAGAA[A/T]ATGAACTGCATAGCA | 1130 |
rs559191568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739695 | GTCAGAGCTTATAGA[C/T]GCTGATGGAATGAGA | 1130 |
rs559206402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235777961 | AGTGTCTTGCTCTGG[A/C]ACCCAGGCTGGAGTG | 1130 |
rs559211966 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235843459 | GGCTGCCTCTTCCAT[A/C]AACTACCCCACAGAG | 1130 |
rs559212864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823468 | CCATTAACTCACTTG[C/T]CAAATCTGAAGAATA | 1130 |
rs559245538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823854 | CTTTTTACACTGTTT[C/T]GTCATCATTTATTTA | 1130 |
rs559249542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815757 | TTCTACAATGAGAAT[C/T]ACAAAACATTGCTGA | 1130 |
rs559254537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699936 | AGAAATAACACCACA[C/G]ATCTACAACCATCTG | 1130 |
rs559268555 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828339 | ATGAAAATATTCCAA[A/C]ATTAACTGTGGTGAC | 1130 |
rs559301784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820131 | AACTATTGTTTAGAC[C/T]GGGTTTTAAACTAAT | 1130 |
rs559343113 | in-del | -/AT | 0.316522 | 0.240987 | intron-variant | LYST | GRCh38.p7 | 1:235805632 | ATAACACAATAATAT[-/AT]ATATATTACATATAT | 1130 |
rs559346130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235713797 | TCAAAAGCCAACAGA[C/T]ATCACTTGAAACTAA | 1130 |
rs559348612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827631 | AAATGTTGATAAAGG[C/T]CTATGTTTTAAATGG | 1130 |
rs559350553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688809 | CTAACATGGTGAAAC[C/T]CCGTCTCTACTAAAC | 1130 |
rs559399945 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867327 | CACAGACTGTCAACC[C/T]GTCCCATTGTGTAGG | 1130 |
rs559404147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673660 | TTAGGTGCTTCTATG[A/G]TCTAGGAGAAAATGC | 1130 |
rs559411531 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823586 | CCATGTCATGGCCTC[C/T]GCCCTTCAGGTCTCC | 1130 |
rs559420304 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687994 | TCTGATCTTTATTCT[C/T]CTTAACTCCCGTTAT | 1130 |
rs559421151 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802456 | ATTCCTGTATTATGT[A/G]TTCTTTATAACAAAC | 1130 |
rs559451322 | in-del | -/AGAC | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235842077 | CTTGGGTCTAATAAT[-/AGAC]AGTGCAGACTGTTAT | 1130 |
rs559469225 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235757715 | GTCACTGTCACTTAT[A/G]CTATTTATTTAAACT | 1130 |
rs559470456 | in-del | -/TATGA | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235789546 | TATGTAAAGCTATGT[-/TATGA]TATATCAAAATCCAA | 1130 |
rs559472773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854663 | AATATCAACATTAAA[C/G]GAGATAATTCATGTA | 1130 |
rs559507929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235699401 | CTTCATCCATGTCCC[C/T]GCAAATGACATGATC | 1130 |
rs559534082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822205 | AGCTGTATATTATGG[G/T]CTAATTGTTATAGAA | 1130 |
rs559562102 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235800065 | GGGCCTAAGCGATCC[C/T]CCCACCTCAGCCTCC | 1130 |
rs559575647 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687557 | TAAAAGATGGGATTA[C/T]GCCTTTGGTACAAAA | 1130 |
rs559579787 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866327 | AGGCGCACGGTGTAG[G/T]TGACAGGTGGGCGAG | 1130 |
rs559598617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799347 | TCTCAAGTTATCTCC[C/T]CACAAGATACTTATT | 1130 |
rs559599435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784624 | TCTCAGTTGCCTCAT[A/G]TGTAAAATTGGGATA | 1130 |
rs559626645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835106 | TATTTTTAATGGGGG[C/G]GGGTTTCGCCACATT | 1130 |
rs559662954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235819749 | CTCCCAGGTTCACAC[C/T]ATTCTCCTGCCTCAG | 1130 |
rs559664776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688288 | TCATCATTCTAAAAA[G/T]TATTTCATCACTACT | 1130 |
rs559680295 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765383 | CCCTAGTTCCTTATT[C/T]CTGAATTCTACTGCA | 1130 |
rs559690875 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235701930 | GTCTTACATAAAGTA[A/G]TATTACAAGGAATAA | 1130 |
rs559692186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834018 | AAATACTATCACGAC[A/C]AAAAGGTTTTCAACT | 1130 |
rs559736029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865742 | AACATCTTTATTAGC[A/G]TAGATGAATCTAGGC | 1130 |
rs559749690 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235698731 | AAAAAAATTTAACTG[A/G]GCGTGGTGGCGGGTG | 1130 |
rs559751044 | snp | G/T | 0.000115465 | 0.00759731 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806029 | AAAGATAATAAATCT[G/T]CCTTCATAGTTCTCT | 1130 |
rs559766531 | in-del | -/A/AA | 0.45762 | 0.139261 | intron-variant | LYST | GRCh38.p7 | 1:235715868 | GCAGTTATCAGAGAT[-/A/AA]AAAAAAAAAAAAGAA | 1130 |
rs559773473 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857580 | ACCAACATGAAGGAG[C/G/T]TGGCAAAGAAGAATC | 1130 |
rs559795878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864862 | TGAGCCTGGGAAGTC[C/G]AGGCTGCAGTAGGTT | 1130 |
rs559796283 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235685858 | CTTAAAACAAAACAA[A/C]AAAAAAAAAACAAAC | 1130 |
rs559813352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235664168 | AATGTAACAAACAAT[C/T]AACAGTAGTTCCCTC | 1130 |
rs559814828 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235790661 | TCTGTCTCATCCAGT[C/T]ATTTCATTCATTCCA | 1130 |
rs559831653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769455 | AGCCCTTAGTGCCAC[C/T]GAAGCAAAGGCGCTC | 1130 |
rs559842159 | in-del | -/T | 0.0879971 | 0.190408 | intron-variant | LYST | GRCh38.p7 | 1:235771599 | TTAATCTATCTTATC[-/T]TTTTTTTTTAGATCT | 1130 |
rs559847558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692473 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 1130 |
rs559849613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789907 | ACTTAATGCTCACAA[C/T]CATCTTATAAGGTAA | 1130 |
rs559851601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235798424 | CTCTTTATAATATCT[A/G]TTCAATTTCTCTGTA | 1130 |
rs559857233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782794 | CATTCCAAAAATGTT[A/G]TGTCATCTATGAGGC | 1130 |
rs559864404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762640 | TACTACATATACTTC[G/T]AAAATATGTACAATT | 1130 |
rs559869925 | snp | A/G | 0.00133074 | 0.0257604 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774935 | ATGTAAAACCCAACA[A/G]TGCATTTTTGTTTGA | 1130 |
rs559874242 | in-del | -/A | 0.479258 | 0.0997024 | intron-variant | LYST | GRCh38.p7 | 1:235816470 | ATAAAAAATAAAAAT[-/A]AAAAAAAAAAAGCCA | 1130 |
rs559874624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235876146 | AGGATCACTTGAACC[C/T]GGGAGGGAGAGGTTG | 1130 |
rs559893676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235762029 | CCTAATGCTAAATGA[C/T]GAGTTAATGGGTGCA | 1130 |
rs559937236 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235847922 | CCTAAGAAATGAGAC[A/G]GCAACACAATAATAG | 1130 |
rs559953136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722147 | CACTGGTGTGCCTGA[C/T]ATTCAAGGCATGGAT | 1130 |
rs559958310 | in-del | -/GC | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235863117 | CTTGAACTTGGCCCA[-/GC]ACGGTGGCTCACGCC | 1130 |
rs559969010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879829 | GCAACCTCTGCCTCC[C/T]GGTTTCAAGTCATTC | 1130 |
rs560001273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679512 | CTTTTAACTTTTTCA[C/T]AAATTTATTTTCTTA | 1130 |
rs560015967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879937 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGGTGA | 1130 |
rs560016567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832345 | AAAAATGTGAAAAAC[C/T]GAAAAATTATGGGAA | 1130 |
rs560020230 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235710374 | GTGTGGCTTCAGGAG[A/C]GGCAGCAGCAGGAAC | 1130 |
rs560052755 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235880592 | TGGAATGTATACATA[A/C]CATGTAGGACTTACT | 1130 |
rs560063605 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235666740 | GAAATAGAATTATAG[A/G]CAATATTTTCCATGA | 1130 |
rs560065706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698085 | CCAAATAGTTCTATT[A/C]TTTTTGTTCTCCTTA | 1130 |
rs560089362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235872538 | TTCCTTCTTCCCGGA[C/T]ACAGGGCAGGATGCC | 1130 |
rs560095292 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705819 | ATTTTTTATACAGGG[C/T]CTCACTCTGTCACCC | 1130 |
rs560104191 | snp | A/G | 0.00066048 | 0.0181605 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804623 | CCTTTGACTGGGAAA[A/G]ATGGTCCCTCATTTC | 1130 |
rs560136753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752651 | TAGGACTAAAAGAGG[C/T]AATAGATTTGCATTT | 1130 |
rs560137439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863236 | TCTCTGCTAAAAACA[C/T]AAAAAATCAGCCGGG | 1130 |
rs560138177 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235851924 | AAACTGAAATCTTCC[A/G]TAAGACAAATCATGA | 1130 |
rs560141054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848217 | TAAAACTGGAAATCA[A/T]CTCCAAAGGGAAGCT | 1130 |
rs560141491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856225 | AATAAGGAAATTACA[C/T]ATTGAAAACCAAACA | 1130 |
rs560150497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877570 | CACCACCACATCCGG[A/C]TAATTTTGTATTTTT | 1130 |
rs560205048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774406 | CCAGAAGTCTCAGAG[A/G]GAAATATTTCCACAA | 1130 |
rs560208963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670218 | GAAAAGTTTAAGTCT[C/T]AGCCAATAATTGGGT | 1130 |
rs560213201 | snp | A/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750969 | AATCTGTGTCTGTTT[A/T]TTTCATCATTGTATC | 1130 |
rs560222929 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235878760 | GATGGGATACAGACA[A/C]CACCATATTTACTGG | 1130 |
rs560231792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704064 | CTCCAGCTCCATACA[C/T]GTTCCAACAAAGGAC | 1130 |
rs560260022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745545 | ACATGTAATTACCGT[A/G]TGACCCAGTAACTGC | 1130 |
rs560268748 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235734023 | GAAAAACAATTGTCC[C/T]TAGGAGACCAGAATA | 1130 |
rs560280112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848850 | AGATACCCTGAACAG[A/G]CCCAGCGAGATTGAA | 1130 |
rs560322282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710515 | TCTGACTCCTGACCC[A/G]AAGCAGACAACTGAC | 1130 |
rs560329903 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661413 | AGCAAATCACTTCAA[C/T]GTGAATAGGAGTAAT | 1130 |
rs560344676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871095 | AGGATGCATATACAT[C/T]TTTTACAATTGTGCG | 1130 |
rs560355634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749897 | TGACCAAATGGGAAA[C/T]AGCAAGAGGACTATT | 1130 |
rs560365918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825570 | AATAAAAAAATTTAA[A/G]TACCATTTATAATAG | 1130 |
rs560370384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235711973 | AAATTTTTAGGACTT[A/C]AAAAAGCTATTTTCA | 1130 |
rs560385976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743482 | TGACCGATTTGTTCC[A/G]TTGTGTCAACTGTAA | 1130 |
rs560391025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676661 | GAATGCTGCCTGATT[C/G]ATGAATCATTAATAA | 1130 |
rs560403342 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817435 | ACACGTATGTTCACC[A/G]CAGCACTATTCACAA | 1130 |
rs560413321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235720073 | CCCAGCTACTCAGAG[G/T]CTGAGGCAGGAGAAT | 1130 |
rs560422820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742621 | AGAAGACATGGACAA[C/T]GAAGCTAAAGTCCTA | 1130 |
rs560437996 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771690 | ACTGAAAAGTACCAT[-/G]AATACCACAAAATCC | 1130 |
rs560438357 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707146 | CGGCCTCATTTGGAC[A/T]CTACTACTACATCCA | 1130 |
rs560443327 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235847060 | CAAAAAGATCTTCGC[C/G]TAGGCACATTGTCAT | 1130 |
rs560446802 | snp | C/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235872356 | TTCAGAAATGAAGAC[C/G/T]GGAAGACCCAGGGAA | 1130 |
rs560468940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235855216 | GAAACCAGATCTTAT[C/T]TGATCAGAAAAATAT | 1130 |
rs560482510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684019 | CTAATACTTAGGTGG[A/G]AAAAAAATCCTATAA | 1130 |
rs560482594 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235831026 | AGCAAACAGAATAGG[C/G]GAACATAAATACAGA | 1130 |
rs560490637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824337 | CACATGTTCATGTAT[A/G]CTAGTCCAATTTTGA | 1130 |
rs560503405 | snp | C/T | 1.66255e-05 | 0.00288314 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788744 | CAGCCCACACTTGGA[C/T]CATCAACGCTTTGGA | 1130 |
rs560529631 | snp | A/C | 0.0984431 | 0.198823 | intron-variant | LYST | GRCh38.p7 | 1:235702053 | TTTAAGGTCCTTTAC[A/C]ACGTCTTTCCCTTAC | 1130 |
rs560531020 | snp | A/G | 3.2994e-05 | 0.00406152 | synonymous-codon | LYST | GRCh38.p7 | 1:235709187 | GATGTTCTGCGACAC[A/G]TAGTCAGACTCTAGA | 1130 |
rs560533010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717854 | GATACAAATTAACAT[C/G]TAAAAACAGAGCAAA | 1130 |
rs560536550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736936 | TCTGAATGTGCTGTT[C/T]CACAACGTTGCTTTT | 1130 |
rs560537584 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235811132 | CCCAGGTGACAGAGT[C/G]AGACTCTGTCTCAAA | 1130 |
rs560540195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831334 | TTCAGCTACAATCCA[C/T]GCTCATCACAAGATG | 1130 |
rs560573769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716948 | CATTCAAAATTATGA[C/T]TTCAGAAATTAAGGT | 1130 |
rs560596018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728285 | ATTTTTGAATAGTAT[A/C]CATGAAGTCTTGGGC | 1130 |
rs560621004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235787819 | AGTAATGTTTGTAAC[A/G]TTTACAAAGTATATA | 1130 |
rs560628399 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832664 | GCATTATATTATAGT[A/T]TACTATGTAGCCAAT | 1130 |
rs560647647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235838297 | CAAGATTGAGTTCCA[C/T]TGTTCAATAACTATA | 1130 |
rs560663560 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235781160 | GCCAGATTCTTTCAG[A/T]TGTTCACTATATTTT | 1130 |
rs560665073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852695 | AATAAAGGAAAACTG[A/C]CAGAGTTCGCATTTA | 1130 |
rs560680167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802651 | TTGTCTTTCACACTA[C/G]AATATACATGAAATT | 1130 |
rs560695454 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235839294 | CAGAATCTCGCTCTG[C/T]CGCCCAGGATGGAGT | 1130 |
rs560724911 | snp | A/G | 0.000132009 | 0.00812324 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809208 | TAAACATCTCCATCT[A/G]CAGTCTCTTCAAATG | 1130 |
rs560739892 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235743235 | ACCTGTATCTGGTTC[-/A]AAACTGGAAGCAGTA | 1130 |
rs560750298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829804 | TAATTATTAGTTCAC[A/G]TAAGAGGTCTCTGCT | 1130 |
rs560769970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235868988 | GCATGAGACACCGCT[C/T]CTGGCCTCGGTTCCA | 1130 |
rs560778476 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235706652 | GAGGAAAAGAAGGCA[-/T]TTTTTTCTCCCTTAC | 1130 |
rs560779661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758888 | TATTATAAGTGGCAT[A/T]ATGAAGACGTTTCCA | 1130 |
rs560801470 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235794604 | CTTGATTTAAAACCT[A/G]AGATAAGTTTTAAAA | 1130 |
rs560808523 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235839148 | GTTCTCTACATATAA[A/T]ATGTAAAAGGTCAGC | 1130 |
rs560818493 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807438 | CCCTTTCATCACAAA[G/T]ATTCAGGTTGTCCAC | 1130 |
rs560823747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772928 | GTTCAAAACTTTGCA[A/T]GGGAAATAAGTGCCA | 1130 |
rs560837937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765138 | CTTCATGCTGTAACC[C/T]TCATTCCCAATTGCC | 1130 |
rs560860242 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830532 | AAGATTGGCTTAAAA[C/T]TACTGGAAATTGGTA | 1130 |
rs560886365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823037 | CCAGAACTGCCAACT[C/G]AACAGAATCATGAGC | 1130 |
rs560888349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235830126 | TGAAAGACTGGACTT[C/T]ATCTCAAGGAGGCTT | 1130 |
rs560901068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667930 | GCCTCCCAAAGTGCA[G/T]GGATTACAGGCATAG | 1130 |
rs560919053 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719742 | CCAGTCTCTAGGAAA[C/T]ACAGGGGTTATGGGA | 1130 |
rs560923543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235734017 | ACAAAGGAAAAACAA[C/T]TGTCCCTAGGAGACC | 1130 |
rs560925262 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235794397 | TCTTTATTCCATCAT[A/G]GGTTTAGCATAAAAC | 1130 |
rs560946443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765976 | CCAATATGTAATTAG[A/T]GCAGCACAGAGGCCA | 1130 |
rs560961372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726188 | AACAGGAAGCTCAGA[A/G]CAAATTTAGGACTCA | 1130 |
rs560979460 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235882799 | TGCCTTGTGTAAAAA[C/T]ATCCCACATGAGTCC | 1130 |
rs560985265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235668609 | TATGACTAGCTGATA[C/T]AATATCACAGATATA | 1130 |
rs560990044 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235816476 | AAATAAAAATAAAAA[A/T]AAAAAGCCATACTGC | 1130 |
rs561017203 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235691552 | GAAGGCAATGCTGAT[C/T]TGGTTCAAACACTAT | 1130 |
rs561019169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674955 | TCATACCTTGTATTC[A/G]TGGATCAAGGCAAAG | 1130 |
rs561038098 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235753699 | TTCTTATCCCAATAC[A/G]ACTTGCCTCTGGGAT | 1130 |
rs561040153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695388 | CCATGGAGGAAACTG[C/T]TCTATTAAACTACTG | 1130 |
rs561055105 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732049 | AACATACCAAAATAC[C/T]GGTAGCGGTTGTTGT | 1130 |
rs561075864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694987 | ATGCAGTGTGTCTCT[C/T]GTGTTAACAAGTGAC | 1130 |
rs561099730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235681575 | GAGAAGGTCAACATA[A/G]GGACCCAGGCAGGAT | 1130 |
rs561101037 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883187 | AACACTTTAACCTAC[A/C]TGAACGGTGATTGCC | 1130 |
rs561101055 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235741201 | CTCTGAAACAGAACT[C/T]CTTAATTTAGGCACT | 1130 |
rs561102260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770566 | ATGTATTTTCAAAAG[A/G]TGAATTATCAAGAGG | 1130 |
rs561118418 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809379 | TTTTTGACAGTGCTC[A/G]TTATTTTCATCACAC | 1130 |
rs561128691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707921 | CTTAGCAGTTCAGTA[C/T]TCTTAATCCAAAAAT | 1130 |
rs561142172 | in-del | -/A | 0.224116 | 0.248656 | intron-variant | LYST | GRCh38.p7 | 1:235770048 | CTGGAGAGAAGATGG[-/A]AAAAAAAAAAGAAAA | 1130 |
rs561142186 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883654 | CGTTGCTTTTTCGTT[C/T]GGTAACGGGGCTAGG | 1130 |
rs561149715 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859479 | GTTTTATTGGGTTTA[A/G]GCTTCTCTCCTGAGC | 1130 |
rs561156418 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235779592 | ATATTTTAACAAGCC[C/T]TCTGGATGATTCTGG | 1130 |
rs561158648 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235772417 | AGACAATCTAGTTTT[C/T]TTTTTGCAAAAATCA | 1130 |
rs561162706 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235726254 | TTTCCAAAACCTTAA[C/T]TTTTTTTTTTAGATT | 1130 |
rs561165197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756348 | TTTCCCCTATGCTCA[A/G]TTCTCTATTAATACT | 1130 |
rs561176964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876184 | CCGAGATCATGTCAC[C/T]GCACTCCATCCTGGG | 1130 |
rs561196532 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806640 | TGGAACTGAGGCATC[C/T]TTCTGTTGCTCCCCT | 1130 |
rs561209220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666691 | GATTATATCTAAATA[C/T]AGCATCAAGATGCAG | 1130 |
rs561210821 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235875576 | ATCATGCTGATGGAA[C/G]GAGTCCTGCCCCACA | 1130 |
rs561231369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682689 | TGAGTCAAAAACCAA[A/T]ACATCAGAAATTGTA | 1130 |
rs561266326 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235666153 | GTGTTGCAGCATTAT[C/T]CACAATAGCCAAGAA | 1130 |
rs561274474 | snp | G/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885337 | TAGGTATATATAGAC[G/T]ACATAGTAGGCAGGC | 1130 |
rs561333902 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235821946 | ACAAAAGTACTACTA[G/T]GAATCTTCAGGGGAT | 1130 |
rs561340163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | LYST | GRCh38.p7 | 1:235740617 | CTTTTTAGAGCTGTA[C/T]AATAGTCTATATGGT | 1130 |
rs561370663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748535 | AATAGAAATCAATTT[A/G]TAAACAGTAGGTAGA | 1130 |
rs561398829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763419 | GACCACTACCTTTCC[G/T]TTATCCATGGCAAAT | 1130 |
rs561420772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881484 | TTCCGGTACATATCA[A/G]AGAGCGAAAGCAGGA | 1130 |
rs561442303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672757 | TTTTCCCGTTACCCT[A/G]TTAAGAGTCTGAACT | 1130 |
rs561462566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701249 | CAGATACAACTTTAA[C/T]AGCTAACGAGCAGTA | 1130 |
rs561470622 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235793807 | ACCAACAAAAACAAC[A/C]AAAACCACTTTTCTT | 1130 |
rs561489749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723625 | CAACATAGAGGTTAC[C/T]GATGACCCTGACGAG | 1130 |
rs561500658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235857507 | TAGAAATAGATGAGA[C/T]CATCAAAGGAAAGCA | 1130 |
rs561590384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732165 | AAACAGTATTATCTT[C/T]ATCTCATCATTTTGA | 1130 |
rs561605571 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778491 | GCAATTCTCCTGCTT[C/T]GGCCTCCTGAGTAGC | 1130 |
rs561634476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834508 | CTCCCAAAGTACTGG[G/T]ATTACAGGCGTGAGC | 1130 |
rs561648366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754330 | CTCTGCCTTCTGGGT[A/T]CAAGCGGTTCTCCTG | 1130 |
rs561649875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235673950 | TTTGCAACAGGCAGA[A/G]CAGAGACCCAAATCG | 1130 |
rs561656373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784446 | GAACATTTCTAATAG[C/T]TTATGGTTCCTCTAC | 1130 |
rs561671313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707398 | TTGGGAGGCTGAGGT[C/G]GTGGATCACGAGGTC | 1130 |
rs561672694 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235851753 | GTACTCACTAAATAG[A/G]GGAAATTAAAATATT | 1130 |
rs561684678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849007 | GGGAACCCTACCTAA[C/T]TCATTATATGAAGCC | 1130 |
rs561687723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783772 | GCCATATATTTCTGC[C/T]ATATTTGTAAGCTGT | 1130 |
rs561700839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235706318 | GTTACCCTCCCTATA[C/T]CTGTAGTAAAGAAGC | 1130 |
rs561720668 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826717 | ACAGGGTTTCACTCT[A/C/G]TCACCCAGGTCAGAG | 1130 |
rs561724750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721852 | AGTAGTGTTCAAAAT[A/T]CTGAAGAACTGGAAC | 1130 |
rs561726565 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791791 | CTCTCAGCTTCATGG[A/G]TACACTCCACATTAA | 1130 |
rs561727395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722852 | CACAATTTTGGAGGT[A/C]AAAAATAATCATCAT | 1130 |
rs561761849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235721261 | GTAGTAGAAACAGCA[C/T]GGTCTTCTGAATTGG | 1130 |
rs561773180 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676670 | CTGATTCATGAATCA[C/T]TAATAAAAGCTAATT | 1130 |
rs561776272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688243 | TTAATAACTAACTTG[C/T]TTTTCTATATCCTGA | 1130 |
rs561780547 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670820 | TCTCCAGGGAAAGGG[G/T]GCAAGAAATCTCTAG | 1130 |
rs561797381 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235871967 | CAAAGACAGATTAAC[-/A]GGAAAAAATATACAA | 1130 |
rs561814031 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235823217 | GGATAGCACCACTGT[-/C]GAGTGGTTAAGATTT | 1130 |
rs561829685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864754 | CTGGGCAACAATGGC[G/T]AAACCCCATCTTTAC | 1130 |
rs561832568 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873383 | TTAACAATTCTGTCC[A/C/T]GTTTTTCTGCTTACA | 1130 |
rs561851549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805308 | GCCCCACAATGATTG[C/T]CCCCACTTCTTAGAG | 1130 |
rs561852604 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235800190 | AGGCTCAAGTGATCC[A/G]CCTGCCACCTCAGCC | 1130 |
rs561863003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856713 | TTCTCCAAAATGTTT[A/T]AATAAGGCTAATAGA | 1130 |
rs561872037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831220 | TCACCTCCCTTCACC[C/T]GCTTCAGGGGGAAGC | 1130 |
rs561876538 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235787998 | CTTATTAGGTAATCG[C/T]TATTAAATATATAAT | 1130 |
rs561889469 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235874377 | ACAAGTAAACAAGCA[A/G]CTATAGTCGAGGGAG | 1130 |
rs561897028 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829418 | CTAAAGCTGGTAACA[A/T]TCAAAGTGTTAAAAA | 1130 |
rs561913506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712825 | ATTTTTTTTCCAGGG[C/T]AGACTATTAATAATA | 1130 |
rs561923248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705581 | TGTAGAGACAGGTTC[C/T]TACCATGTTGCTCAG | 1130 |
rs561971243 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822861 | ATGTAAAGAAGCTGA[C/G]TCTAGCCTACTGAAA | 1130 |
rs561993843 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722011 | TACTTTATAGAGTCA[C/G]GGAGGGCCTCTCTGA | 1130 |
rs562005040 | snp | A/C | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854098 | CCTCCTCAAAAGAGA[A/C]CTTTGGATTTTTATA | 1130 |
rs562013272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775653 | TTCTGATCCCTCTCT[G/T]CTTGGTTTAAGGGAA | 1130 |
rs562016296 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235847347 | GAATTCGCCATCACC[A/C]AGCCACCACTAGAAG | 1130 |
rs562041145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832178 | TTAAAAACTCAACAG[A/G]TATAGTACCAGCAAT | 1130 |
rs562077916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833261 | ATTGCACGGTATTTT[A/C]TTTAAATTTTTTCTA | 1130 |
rs562078193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235825860 | AAATATGAAGGATCT[A/T]GAATGGCCAAACTTT | 1130 |
rs562097727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681099 | TTTCACAAAGAACTC[C/T]GGGGACCCACAGATA | 1130 |
rs562101410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670500 | AGGGTCTCCAATCAT[C/T]TCTTGTGAGGAGACG | 1130 |
rs562105135 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753839 | TAATGCACAATTGTT[G/T]CGTGAAAGCCAAAAG | 1130 |
rs562114094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685253 | GTGTGGGCCTGTCTT[A/G]GAGCATACACTCCAC | 1130 |
rs562114448 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235705627 | CTGGCCTCAAGCGAT[-/C]ATCCTGCCTCAGTCT | 1130 |
rs562123450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819693 | ACTCTGCCACCCAGC[A/T]GGAGTGCAGTGGCGT | 1130 |
rs562131101 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235824795 | GGGTGGCTGAGGCGG[C/G]TGGATCACGAGGTCA | 1130 |
rs562157954 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235872080 | GCGGGTGGATCACCG[C/G]AAGTCAGGAGTTCGT | 1130 |
rs562170467 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235732989 | AGTCATCTATCCTTC[-/AA]AGAGTTGACAAATAT | 1130 |
rs562181529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235737150 | TTTCACTGTATAACC[A/G]TAATAGTATGCTAAG | 1130 |
rs562188323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235812824 | AGGAAAAATGTGTTT[A/G]CCTAAATAATTTTTC | 1130 |
rs562189157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235671203 | TCAGCCTCCCAAAGC[A/G]TTGGGATTACAGGTG | 1130 |
rs562190196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761363 | AAAAGGACAGTAGTC[A/G]GGAAAGGAAAAGATG | 1130 |
rs562214458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878981 | TTAGAGTACCCATCA[A/C]CTGAATAGTGAACAT | 1130 |
rs562224951 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235768675 | TGAAAAAATATATGG[A/G]AATCTCAAAGTTTAT | 1130 |
rs562231902 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235767742 | CTCACTGCCTTCAAT[A/G]ATCTGCCACACATGC | 1130 |
rs562233839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698053 | GAAAAGACATGATGC[C/T]CTTTTAAAGAGTTTC | 1130 |
rs562243314 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235729968 | CAAACATTGTTTCAT[G/T]CCTCTGATACTTCAG | 1130 |
rs562271711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839366 | GGTTCAAGTTGGCCA[C/G]GCTGATCTCAAACTC | 1130 |
rs562277178 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789747 | TTTGAGGCTGCTGAC[C/G/T]AAGATATATGATATA | 1130 |
rs562293905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235744758 | ATACAAAAATTAGCC[A/G]GGCATGGGGTGCACA | 1130 |
rs562342276 | snp | A/G | | | missense, intron-variant | LYST | GRCh38.p7 | 1:235702854 | TGAGCTTGGCTCCAG[A/G]TCTGCTCACATGGGC | 1130 |
rs562343201 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235872066 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACCGGA | 1130 |
rs562356201 | snp | C/T | 4.98186e-05 | 0.00499067 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775040 | AATGAGAGTATAACT[C/T]GCAGTGCTAATGCTT | 1130 |
rs562358125 | in-del | -/A | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739896 | ACGACAACCACAGTT[-/A]AAAATTTCAAGCTGA | 1130 |
rs562361923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782726 | CACCTCCCCTTAATT[G/T]TGCCAAGAAGTCTCC | 1130 |
rs562380488 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235676563 | GAGTTTTGTTCCTTG[C/T]TTCTGCTTTCTTCAG | 1130 |
rs562398095 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235782200 | TTTTTTTTTTTGGAG[A/G]CAGAGTCTCGCTCTG | 1130 |
rs562403190 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235669774 | TACTTTCATTTTCAA[A/T]AAATTCCTGCTTTTG | 1130 |
rs562403620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678417 | GGCCCTAATGCTACC[C/G]ATACTCAGCAGTTAT | 1130 |
rs562411833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879872 | CTCCCAAGTAGCTGG[A/G]ATTATGGGCATGCGC | 1130 |
rs562415703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685815 | CACACCATTGCACTC[C/T]GGCCTGGGCGACAGA | 1130 |
rs562418362 | snp | C/T | 0.000166284 | 0.00911671 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744136 | GGAGTTCTCAAAATG[C/T]CAATAATGTCTGAAT | 1130 |
rs562424738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854395 | ATTCTCCAAAGCAGA[C/T]ATTGACTTCTCTCTC | 1130 |
rs562434853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847445 | AGCATAAATCACACA[C/G]GGCCTATAGAACAAA | 1130 |
rs562458119 | snp | C/T | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660930 | ATCTTTTTCTAGTGA[C/T]ATAAATGCATAGTGG | 1130 |
rs562466348 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235844478 | ATCCCAGTTGTCTTG[A/G]AGTTACATATGTTTT | 1130 |
rs562472880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235703919 | TCCTCCTATCCCTCA[C/T]CCTAAAATAGGCACC | 1130 |
rs562478917 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695295 | AGGATTTGCAAAGCA[C/T]GAAGTTAACTTCCCC | 1130 |
rs562496399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773738 | AACACTGTAAATGCA[A/C]TTAATGCCACTGAAC | 1130 |
rs562514999 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235860177 | TCTATCCTCTTTTTT[-/A]AAAAAAAGACTTTAT | 1130 |
rs562518453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824219 | TTTGGTAAAACTTCA[C/T]ATTTTACTCAGCAAC | 1130 |
rs562543235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752505 | ACACATAGGCAGTTT[C/T]TAGTCCACACTAAGG | 1130 |
rs562571165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751793 | TTCACTTATGTATTG[C/T]CAACTACTAACTACA | 1130 |
rs562601702 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661401 | TTTTGTTAACAAAGC[A/G]AATCACTTCAACGTG | 1130 |
rs562614884 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884570 | GGATACTGCCACTAG[C/G]TTTCTGGTGGCAAAC | 1130 |
rs562648757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719041 | TTTATTTTTTGAGAC[C/G]GAGTTTCACTCTTGT | 1130 |
rs562652360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697677 | GACCACATGTAGCAC[A/T]GGAAACCTCACTCAG | 1130 |
rs562670421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787619 | CATAATTTAGGCAAT[A/C]ATGTTCAGAATTCAG | 1130 |
rs562692390 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235765395 | ATTCCTGAATTCTAC[-/T]GCAATAATTTACTTA | 1130 |
rs562706890 | snp | A/G | 0.000101327 | 0.00711712 | intron-variant | LYST | GRCh38.p7 | 1:235792164 | AAACTTTCTAATCAC[A/G]TAATAAAGTACATAA | 1130 |
rs562727824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235735085 | ATTTTTTCATATAAA[A/G]TATATTTTAAAAAGC | 1130 |
rs562743663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235786841 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 1130 |
rs562749301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235877765 | CTGAGACAATTGCAT[C/T]GCTTAGCAGTGTAGA | 1130 |
rs562778977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766663 | TTTCTTTGTCTATGT[A/G]AGTAATACTAGTGCT | 1130 |
rs562784963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870439 | ACTTCCATTTTCTGT[A/G]TGTCACTTTCCTTTT | 1130 |
rs562788055 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235860416 | TATTCTATGGGTATC[A/G]ACAAATGTATAATAA | 1130 |
rs562790451 | snp | A/C | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757423 | AGGAGTTCATATAAT[A/C]CACAGCATATAGGTA | 1130 |
rs562790696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235863157 | AGGCACAGTTGGGGG[C/T]CGAGGAGGGCAGATG | 1130 |
rs562813638 | snp | A/G | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662738 | TTGACACAATCTTCC[A/G]GATTATCACTAAAAT | 1130 |
rs562816775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749842 | GGTGACAAAATGCTA[A/G]TATCTAAAGAGAGAG | 1130 |
rs562829678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837512 | CACACCTGTAATCCT[A/C]GCTACTTGGGAGGAT | 1130 |
rs562848959 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235877502 | ACCTCTGCCTCCCGG[C/G]TTCAAGCAATTCTCC | 1130 |
rs562851378 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235683137 | CCTAATAGTAGTATT[G/T]GATAATTTTTTAATA | 1130 |
rs562854401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758176 | TCAGCTCCATATAAA[A/G]TTATGGGTCTGCGAT | 1130 |
rs562915674 | in-del | -/AACC | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235692338 | CTTCATCTCATAACA[-/AACC]AACCAACCAACCAAC | 1130 |
rs562922793 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | LYST | GRCh38.p7 | 1:235792703 | AGTTTAGCTCTTGTT[A/G]CCCAGGCTGGAGTGC | 1130 |
rs562925020 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235831962 | TGACACAATGCTTCT[C/T]ATCACATAAAATTTC | 1130 |
rs562925209 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235725200 | GCACTTTGGGAGGCG[C/G]AGGCAGGCAGATCAC | 1130 |
rs562941868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709029 | AATGGCCGAACAACT[A/G]ACCTTAAAATATTCA | 1130 |
rs562958068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235724602 | CATTCCATGGGTTTT[C/G]ACAAATGTATAATGA | 1130 |
rs562961895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235733754 | TTTATCAGAACATGA[C/T]ACTTTAAAACTAAAA | 1130 |
rs562969497 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830313 | TGCCATGTGCGTCTC[C/T]TCCTCTTCTTCCTCC | 1130 |
rs562985846 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762607 | GCTGGGTGTCTCTTG[C/T]TAGATTGAATGAGGT | 1130 |
rs563022245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852659 | TCAACTAATACTGAG[A/G]TAAGTGACAAGTTGA | 1130 |
rs563076411 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235833695 | AGACATATTAATCAC[A/G]ATAGTAAACCACAAA | 1130 |
rs563095132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694847 | CATCTTTTTTTTTTT[C/G]TTTCAGAAAAAGAAA | 1130 |
rs563096666 | snp | C/T | 3.36876e-05 | 0.00410398 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808430 | AACAACCCCCGCCCC[C/T]GCCGCCACCCACACA | 1130 |
rs563116848 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873545 | GTTTTAGTAGACACA[C/G]ACACAAACACACATA | 1130 |
rs563144986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764797 | CGTGAGCCACCGTGC[C/G]TGGCCCCATTTACTA | 1130 |
rs563148091 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838352 | TCATGTTCCCAAGTA[C/T]AGAATGGTGGACTGT | 1130 |
rs563165119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235696161 | AACAACTATAAAACA[A/G]TCATTCATTTCATGA | 1130 |
rs563201037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701922 | AGTGTTCTGTCTTAC[A/G]TAAAGTAATATTACA | 1130 |
rs563222490 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235750045 | AAAGGTATACTTTCT[A/G]ATATCAAGAGAGGGC | 1130 |
rs563225930 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235794234 | GTTAAGCTAATGCTT[C/T]TATATCATAAAATAG | 1130 |
rs563233964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235778676 | ACAAGCATGAGCCAC[C/T]GTGCCTGGCCTGTGC | 1130 |
rs563235583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835889 | TTTACCTTTCATAGC[C/T]ATAATGCCCAATTTT | 1130 |
rs563258580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682274 | AGGCTGCAGTAAGCC[A/G]TGATTGTGCCACTGT | 1130 |
rs563280050 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235836477 | TAATATTTGAGCAAA[A/C]ACTTGAATGGAATAA | 1130 |
rs563308983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674144 | CAAGTAACAATGTCA[A/G]TTTTACCTTGTGTCT | 1130 |
rs563310448 | snp | A/G | | | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830400 | TTCACGTGCCAGTGA[A/G]TTACTGTCGGTGCTC | 1130 |
rs563310766 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235870375 | GTTTGAACTGTGTTC[C/T]AATAAAGCAAACGCT | 1130 |
rs563328527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740548 | GGCTGTCCCTTTCCC[C/T]ACTCAATGTTTCTGA | 1130 |
rs563362095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667827 | GCCACCATGTCTGGC[C/T]AAATTTTTGAATTTT | 1130 |
rs563371575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235748386 | TAATAGCAAAAACCA[A/C]GCAAAAAAACCTTTG | 1130 |
rs563375247 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235721262 | TAGTAGAAACAGCAC[G/T]GTCTTCTGAATTGGA | 1130 |
rs563394939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666837 | TAATTAGATAAGTAC[C/T]AGTAAGGCTAGAAGG | 1130 |
rs563398137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235806970 | TAATTACTCTGATAT[C/T]CTTCTTCAAACATTT | 1130 |
rs563432456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700459 | AGAATATTTAAAGAG[C/G]AGTGCTTTATTGAAA | 1130 |
rs563461128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843590 | CAGACAGTGCCATCT[A/G]AAGGAAGAAAAAGAT | 1130 |
rs563467312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235699997 | TGGGGAAAGGATTCC[C/T]TATTTAATAAGTGGT | 1130 |
rs563471968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688324 | ATTATTCCTAAATAC[A/G]CAAAAAACAAACAAA | 1130 |
rs563502748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680292 | ACAGGGTCTCACTCC[A/G]TCACCCAGGCTGCAG | 1130 |
rs563504034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792955 | AGGTATGAGCCATGG[C/T]GCCCTGCCTTAGATG | 1130 |
rs563511958 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235761221 | GAAAACAAAACTAGA[A/G]ACTAATACCTATATA | 1130 |
rs563544243 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884845 | AAGCCCAGGCCAGAG[C/T]GCAGTTGTGTGACCT | 1130 |
rs563558053 | snp | G/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235666099 | TTTATTTAAAAATAT[G/T]CCAAAGACCGCCAAA | 1130 |
rs563562912 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758456 | TCATCCAGAGAAGAA[C/T]TGCCAATGTTCAGCA | 1130 |
rs563569518 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235882401 | GCGGAAGCTTTGGAC[G/T]TTATTCCATAGGTAC | 1130 |
rs563590948 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235694251 | AACTCCTGACCTCAA[A/G]TGATCTGCCCGCCTC | 1130 |
rs563606585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874460 | ACACCCAACTCCCAT[C/T]CTGGGATCATAAAAA | 1130 |
rs563607353 | in-del | -/TATAT | | | intron-variant | LYST | GRCh38.p7 | 1:235881605 | ATAAAGAAAATGTGA[-/TATAT]TATATATATCACTGT | 1130 |
rs563636954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829257 | CATGACAAGTAAATG[C/T]TTCCTAATTTGTATT | 1130 |
rs563641989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672670 | ATTTGATTACTTTTA[C/T]AACTAAAGAAACTTT | 1130 |
rs563739193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828234 | TAAAATCTGGAGAGA[C/T]AGAAAGTAGATTAGT | 1130 |
rs563759928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881419 | ATGCACAATCGGCTT[C/T]GAGGAAAAATAATAG | 1130 |
rs563778379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235670663 | AAGGTAAGAAAAGCC[A/G]CAGGGGCAGTGAAGT | 1130 |
rs563787748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850360 | CCTCATCTCTCACCT[C/T]ATACAAAAAATCAAC | 1130 |
rs563803939 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743699 | AGTCATCAATGATGA[C/T]GATCTACTCTTTTCT | 1130 |
rs563814572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235770375 | GGAAGACACACAACG[C/T]GCAACAATTTAACAT | 1130 |
rs563832798 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | LYST | GRCh38.p7 | 1:235697542 | GAAATTTGAGCAGAG[-/A]AAAAAATTTAGTACA | 1130 |
rs563846763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776934 | ACATTTTAATATGTA[A/T]TTTTTTTATGTTAAA | 1130 |
rs563863612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776428 | ACGAAGATGGCATTC[C/T]GAGGATGAAGGAAGA | 1130 |
rs563880928 | in-del | -/CG | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235801416 | TTCAAACTTTCTGAC[-/CG]CCCCCCCTCAAATAC | 1130 |
rs563887225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849452 | TTCCCTCTGAGAATT[A/G]AAACAAGACAAGGAT | 1130 |
rs563890545 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731131 | GCCCTTCTGTTGGAT[C/T]CAACTGCCATGAGGT | 1130 |
rs563894652 | in-del | -/T | 0.0410537 | 0.137264 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884289 | ACTACGCCCGGCTAA[-/T]TTTTTTGTATTTTTA | 1130 |
rs563902979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872621 | ATTTTTTTATGGCCA[C/G]CTTCTATTCAGAAAG | 1130 |
rs563907360 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235709427 | AACCAAAAAAGGGAA[-/G]TAGCAAGGAGGATTT | 1130 |
rs563914318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820241 | ATCACAAACCGGACT[A/G]ATGTCTAGGAAGCTG | 1130 |
rs563972159 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677373 | AGCATGTGTTTCATG[A/G/T]TTAAAATGATTATAA | 1130 |
rs563979978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864717 | TGGATGGATCGCTTG[A/C]GCCCAGGAGTTTGAG | 1130 |
rs563997777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665375 | AGCACTTTTGGAGGC[C/T]GAGGCGGGTGGATCA | 1130 |
rs564010619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235753680 | AAAGGGAATGATTCT[C/T]GAGTTCTTATCCCAA | 1130 |
rs564012943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723495 | AGAGAAAATGGTAAC[C/T]CAGAAGCCCAGGGAG | 1130 |
rs564024459 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235665139 | GAGACAATAACCAGC[A/G]AAAAAATAAAAATAA | 1130 |
rs564047445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761272 | TTACCATCTCACCTG[C/T]AGTATTTAATAATTA | 1130 |
rs564067016 | in-del | -/A | 0.40853 | 0.193309 | intron-variant | LYST | GRCh38.p7 | 1:235744905 | CTCAAAAAAAAAAAG[-/A]AAAAAAAAAAGAGAG | 1130 |
rs564086239 | in-del | -/TGCCCTCCCTCTTCCG | 0.121369 | 0.214369 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865325 | GCCCTCCCTCTTCCC[-/TGCCCTCCCTCTTCCG]TGCTTTTTCTCTGTA | 1130 |
rs564091086 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235759858 | CTGGACTCAAGACAG[-/C]CTCCCACCTCAGACT | 1130 |
rs564101395 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738256 | AAGACTATACTGTAA[A/C]TGTAAACTCCAAGCT | 1130 |
rs564108007 | snp | A/G | 0.000152694 | 0.00873634 | intron-variant | LYST | GRCh38.p7 | 1:235804676 | AAGTTCTAAGGTAAA[A/G]TAAAAGAGACTAAGA | 1130 |
rs564111943 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875804 | GAGGTATGGTACTCA[A/G]GCCTGGGTGACAGAG | 1130 |
rs564115838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798533 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 1130 |
rs564125253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695728 | AGCTCCGCCTCATGG[A/G]TTCACGCCATTCTCC | 1130 |
rs564125612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235730290 | TTAATACTCAACAAC[A/G]CTATGATACCTATTA | 1130 |
rs564155630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728390 | TACTATGGAAATTAA[A/G]TTAGAATATATGCAA | 1130 |
rs564169668 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235762997 | TTTATATTAAGGCAC[A/G]CGATATGTGAATACT | 1130 |
rs564170907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833492 | AGCTGTTTTAACTTT[A/G]GGGTTTAACGAATGT | 1130 |
rs564171313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768447 | TTTATTAATCTTCCT[A/G]AAGTGCACAAACACT | 1130 |
rs564173397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235855302 | TTTAATACTAACTTT[C/G]ATAGAAAACATTTTA | 1130 |
rs564208438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871141 | TGAAACTTTATTGAA[C/G]AGGTCAATTCATAAT | 1130 |
rs564231726 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235711012 | TGAAGGCAACAGCAT[A/G]AGACACCCTGAGCTA | 1130 |
rs564232946 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235752739 | ATCTTGATAATCTAC[C/T]TCAATGTACGATATT | 1130 |
rs564237588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704956 | TCTAAGTGAACCCCA[C/T]GTATTAGTGAACGGT | 1130 |
rs564244118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864050 | CTTCAGCAAGAATCC[C/T]GTTAGGTCGGCTTAG | 1130 |
rs564284191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774477 | TGATGATAGCGGGAT[A/C]ATAATAAAAATGAGC | 1130 |
rs564287780 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | LYST | GRCh38.p7 | 1:235794524 | TTTATTTCAGCTGAT[C/T]CTCACCAAAAACAAA | 1130 |
rs564288205 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685718 | GGGTGTGGTGGTGTG[A/C]GCCTGTAATCCCAAC | 1130 |
rs564290805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811721 | AATCTGTGCTTTACT[A/G]AGACAGGGAAAGCAA | 1130 |
rs564299416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235847345 | GAGAATTCGCCATCA[C/T]CAAGCCACCACTAGA | 1130 |
rs564302387 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235720203 | AAAAAAAAAAAAAAA[G/T]GCTATTCTAGGTATA | 1130 |
rs564308044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712717 | TGCGTAGGTTACGGT[A/G]CATTGTTTTTTGGTG | 1130 |
rs564316677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878155 | TTCACACGTGTTGGC[A/G]AGGTAGGGTAGCTTA | 1130 |
rs564330632 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235663165 | CTGAGGTTAGTGTAA[A/C]GAAGTTATCTTCAGT | 1130 |
rs564391629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856407 | TAGGATCTCAGGCAA[A/G]GTGCTTAACCTTTCT | 1130 |
rs564394467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736977 | AGACATTTCACATGA[C/T]TAAAAACAAAATTAA | 1130 |
rs564415734 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864813 | GTGTGCCTGAAGTCC[C/T]AATTACTTCAGAGGC | 1130 |
rs564420085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705505 | ATCCTACTGCCTCAG[C/T]CTTTTGAGTAGCTAA | 1130 |
rs564428626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848901 | ACTAAAAAAAAAGTC[C/T]AGGACCAGACAGATT | 1130 |
rs564437830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839295 | AGAATCTCGCTCTGT[C/T]GCCCAGGATGGAGTG | 1130 |
rs564464208 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718827 | AGTAAGGAATTGGTG[A/C]CCTATTACCTCTAAT | 1130 |
rs564494520 | snp | G/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739662 | AGTTGACAAGGGAAA[G/T]TTCTTCCCTATAGTA | 1130 |
rs564514579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825742 | ACTCAACATTGTTAA[A/G]TGTCAATTCTCTGTA | 1130 |
rs564518745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235816611 | GAATAGCCAAAGCAA[C/T]CCTATACAAAAAGAA | 1130 |
rs564574022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678386 | ATGCAAATTGGTGAT[A/G]TTACCAACGGTAATG | 1130 |
rs564590894 | in-del | -/TCAGT | | | intron-variant | LYST | GRCh38.p7 | 1:235839504 | CACATTATTTAAAAA[-/TCAGT]TCATGCTGGGCATGG | 1130 |
rs564591088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767801 | GCCTTATCCATGCTA[C/T]TGAAATCTTGTAAGT | 1130 |
rs564593588 | snp | C/T | 9.96429e-05 | 0.00705773 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809908 | GACTCTCCAAGTTGT[C/T]GCTCAGACTGCAGCA | 1130 |
rs564616172 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235818993 | ATTGCTGTTCTCCCC[A/C/G]TCAAGAGAAAGGAAG | 1130 |
rs564628091 | snp | A/T | 1.66466e-05 | 0.00288496 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775009 | TTCATGTACTCTTTG[A/T]TGGTTGTATTTAATT | 1130 |
rs564636998 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732668 | AAAAGTAAAATGTGG[C/T]ATCTAGAGGTTCTAG | 1130 |
rs564649104 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869469 | AGAGCGAGACTCCGT[C/G]TCAAAAAAAAAAATA | 1130 |
rs564659638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831453 | ATGTCCTGAAAGGTC[A/G]CGCAGAGATGGGGCT | 1130 |
rs564662353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846440 | AACCAGAAAACCAAC[A/C]CTGGTAATATGACAA | 1130 |
rs564667006 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235699317 | TGTTCAACTCCCACT[C/T]ATGAGTGAGAACAAG | 1130 |
rs564673397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796715 | TTCTGCATTTTGCCA[C/T]GTGAGGATGCAGCAA | 1130 |
rs564675190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697604 | AAGTTGATACTTACT[A/G]GAGGACTGTAATTTG | 1130 |
rs564704858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682907 | CATCAAAACTAAAAT[A/G]AGGTTAGCGTTCTAC | 1130 |
rs564705545 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235775956 | TAAAAACATACTTTA[A/T]AAGTCTTATTGGCAA | 1130 |
rs564710699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803860 | AAAACATTATATATA[C/T]GGCTAGATCAAGGAG | 1130 |
rs564736860 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235737560 | TTGGGGAAGGAATTG[A/C]ATAAGGTGGGCCTGG | 1130 |
rs564745712 | snp | C/T | 4.9476e-05 | 0.00497348 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809277 | AGACCTGAGAGATCT[C/T]GGTGATGATGCATAA | 1130 |
rs564746592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685175 | CCTTAGGATCCAGCT[C/T]AAGTGTAACTTAACA | 1130 |
rs564764706 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235789661 | AGGTAAAACCATGAC[C/T]GATGTTAAAAAAATA | 1130 |
rs564776442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862285 | CCTTTTCAGTGTATA[C/T]GGTAGTATCCCTTTA | 1130 |
rs564799077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750961 | AGGGGCAGAATCTGT[A/G]TCTGTTTTTTTCATC | 1130 |
rs564813462 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853621 | TGTCAATAAACAACA[C/T]TGCCTATTTCGCTAC | 1130 |
rs564839638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675789 | TGAGGGTGGGGCTCA[C/T]GGCAGCCTCCAAATT | 1130 |
rs564864367 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235729736 | TTTATTTTACCTAGT[A/G]AAAGATTTCTGCAAA | 1130 |
rs564875493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803286 | TTTCTAACAAAGTAA[A/G]TTATAGGTCATTTCA | 1130 |
rs564878287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815938 | GAGATCGAGACCATC[A/C]CGGCCAACTGGTGAA | 1130 |
rs564892288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779681 | TTTAGGATAGGATCA[C/T]TCTTTGTTGTATAAT | 1130 |
rs564906825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794504 | TTCAAAGTATTTTTA[C/T]ATGCTTTATTTCAGC | 1130 |
rs564927077 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235669191 | ACTACATAGCTTCAG[G/T]CTAGAGGCTGGTCAC | 1130 |
rs564928617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235726392 | AATGTAATATTTTCA[C/T]ACTTAAAACTGAATT | 1130 |
rs564946092 | snp | A/C/T | 4.9442e-05 | 0.00497182 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759377 | AATGCGTCCTCTTTG[A/C/T]CTTTTTTCAGTGTGT | 1130 |
rs565009499 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661288 | AGATAAATGATGAAA[C/T]TCGGTTTTTAAAAAA | 1130 |
rs565015779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854269 | AGTTGACACATATTG[C/G]AAACTGAAGCACAGT | 1130 |
rs565016266 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235682384 | AGGTGCCTTAGCTCA[A/C]CAGGCTGCTGGCGGA | 1130 |
rs565036778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786788 | ATCACTCTCAGCAAA[C/T]GATCGCAAGGACAAA | 1130 |
rs565041302 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235731684 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 1130 |
rs565051642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235773155 | AAACCCTGTCTACAC[C/T]CAAAATACTAAAACT | 1130 |
rs565097114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799705 | AGTACAGATTAATCA[A/G]TACCAGATATGGCAA | 1130 |
rs565103491 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235876453 | TCCCAAGTAACCAAG[A/G]TAGTAGTTGCTCAAT | 1130 |
rs565106964 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818979 | CACACGAACCCAAGA[C/T]TGCTGTTCTCCCCCT | 1130 |
rs565108512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235695471 | TAAGTGTAATTTGAG[C/T]GAACATAGCTATTAA | 1130 |
rs565109560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235734838 | GCACTGAGTATTTGA[C/T]GACAGAGGATTAATG | 1130 |
rs565114550 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884498 | CCCCAGTCTCCCAAA[A/G]CCATGGTTTACAGAC | 1130 |
rs565117483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694462 | CTGTAAATGGTACTG[C/T]CCTTGAAACTTGCAA | 1130 |
rs565141122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877245 | AGCACCACACACCAG[C/T]CATGACAGAGAGGGG | 1130 |
rs565142736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235869069 | AACATCGATACTAAA[C/T]ATACATATCAAATAA | 1130 |
rs565143719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801924 | GCAGTGGCTGGGTGC[A/G]GTGGCTCACGCCTGT | 1130 |
rs565159827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235765330 | GCCCAGATTCTGTTA[C/T]CCTGTCTCTCACGGA | 1130 |
rs565160837 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235833522 | TCAGATAATTATGTA[C/G]TTTCAAGCCTTCAAA | 1130 |
rs565168650 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235773662 | TTGTTTAAAGGGTAC[A/T]AAGTTTTGGTTTTAC | 1130 |
rs565183208 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235692779 | TAATCCCAGCACTCT[A/G]GGAGGCCAAGGCGGG | 1130 |
rs565210235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780176 | TTTGGGAGGCTGAGA[C/T]GGGAAGATCGCTTGA | 1130 |
rs565226170 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824151 | TAGCCAAAGATTTTT[A/T]AAAACCTATTATAAT | 1130 |
rs565244772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852497 | CCGGGGAAGTCTCAC[A/G]ATGCAACACTCAAGT | 1130 |
rs565254852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802383 | CATCCTAAAGACAAA[C/T]TGAGCTGTGGTAAAC | 1130 |
rs565263427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837448 | GCCTGGGCAACATGG[C/T]GAAATCCCATCTCTA | 1130 |
rs565272770 | snp | C/G | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741429 | ATACTTACTTGTAGG[C/G]ATGGGCTGAGACAGT | 1130 |
rs565277099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749792 | AACTAAAAAAAAATA[A/G]TAAACTTGAAGTTAC | 1130 |
rs565292899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769812 | AAGCAATACATATTT[A/G]TAAATATTTATTTAA | 1130 |
rs565334488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734226 | GTATGCTTCAGCTTG[C/T]TTGTCACTTTAAAAA | 1130 |
rs565334578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742258 | TCAGGAGTTCAAGAC[C/T]AACCTGGACAACATG | 1130 |
rs565357723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235715887 | AAAAAAAAAGAATAT[A/G]GTGATTTTTCACTAC | 1130 |
rs565377914 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868077 | CCCCACTTTAAAATA[G/T]GTCTTCTCTGACGTC | 1130 |
rs565392402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807625 | ACGAAGATATTGATA[G/T]GTTATTTTTGTATAA | 1130 |
rs565413343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695976 | AATAATTCACACATG[C/T]TGGTACTTTGGTATT | 1130 |
rs565457259 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762311 | AAAGTCCAAGACAGA[C/T]GCATGCAGAGCGGTA | 1130 |
rs565457315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235770666 | TGTTGTTAAAAATGT[A/G]CACATTTCAATACCA | 1130 |
rs565457666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814547 | CAAGGAAGAGACCAG[G/T]TCAGGAAAGAAAGGA | 1130 |
rs565458370 | snp | C/T | 0.000167151 | 0.00914044 | intron-variant | LYST | GRCh38.p7 | 1:235716818 | AATTAAATATTTTGA[C/T]ACTGTCAAGATTAAG | 1130 |
rs565459752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822804 | CATGTTGTTATGTGA[C/T]TTCTTGCAGCTTCTG | 1130 |
rs565488859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860315 | CCCCTAAACTGGTAC[A/C]TTTGTTATAATCAAT | 1130 |
rs565495530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815177 | TTTTCCTCTTTTATC[C/T]GTTAAACAAATATTT | 1130 |
rs565499060 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235745396 | ACATCTGTCAGAATG[C/G]CTAAAATAAAAAATA | 1130 |
rs565506033 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235678381 | GTGTCATGCAAATTG[C/G]TGATGTTACCAACGG | 1130 |
rs565522578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858790 | CTACTTGTTTTCTGC[A/G]TTGTTATGGGGGTGG | 1130 |
rs565526277 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884760 | ATTTTTATTTAGAAA[C/T]TTTTGTACATATATA | 1130 |
rs565559579 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862936 | TTATAAAATGAGGTG[C/T]TGCCTGATTCTACAA | 1130 |
rs565568362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738503 | CAATCTGGACTCAGC[A/C]CAATTCCGTTACCCA | 1130 |
rs565573369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235723006 | TAGTGGCTTAAACCA[A/G]GATGGTAGCAGTGGA | 1130 |
rs565579762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756528 | AAATGCGAGCTCAAT[A/G]CTAGGTTGTATTGCA | 1130 |
rs565587999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235667724 | CAGACTGGAGTGCAG[C/T]GGTACAATCTCAGCT | 1130 |
rs565590481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235880982 | AATAAAAAAATTAGC[C/T]GGGCGTGGTGGAGGG | 1130 |
rs565601746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851951 | ATGATCCCATATTTA[A/T]TGACTACTCACCATA | 1130 |
rs565628105 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235785832 | CAATGCTTACAAATC[A/G]AAGATACCTTATAGT | 1130 |
rs565628393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708895 | GGGGATTGTTTTGGG[A/G]CACCTCTGAAAAAGA | 1130 |
rs565628664 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235700670 | GTCGAAAGTTTCACC[A/G]TGGTTCAAATAAAGA | 1130 |
rs565645091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739016 | GTCATACTATTTCAC[C/T]GTCTAGGCTACAATA | 1130 |
rs565646693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235820454 | GGCTCACTGCAACCT[C/T]CACTGCCCAGGCTCA | 1130 |
rs565652433 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235825795 | CATCTTAAATGAAAT[C/T]CTAGTGTGCATTTTG | 1130 |
rs565674930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813120 | GACACATCAGTTCCT[A/C]ATGTCTTGTCTTAAA | 1130 |
rs565677331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714754 | CACAGTGAAGTTGCC[A/G]GTGTGCGTCTTTTAT | 1130 |
rs565716968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235670342 | GCTCTTGCAATCAGA[C/T]GGATGCAGGCAGCAC | 1130 |
rs565751888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755029 | CAATGAGCTGAGGCA[G/T]GACTGTGTCTCTCTG | 1130 |
rs565766930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820114 | GCACTGGCCCTTTTC[A/T]TAACTATTGTTTAGA | 1130 |
rs565785016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848495 | ACAAAGCAAACCCAA[A/G]CCCAGCAGAAGAAAG | 1130 |
rs565805096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235745993 | CTGGTGATGATATTA[C/T]ACTACAGTTCTGCAA | 1130 |
rs565821726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849067 | GGACATAACCAAAAA[C/G]AGAAAACTACAGAAC | 1130 |
rs565824126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813617 | CTTTCTGGAGGATAT[C/G]GTCCAAGCCCTGGAG | 1130 |
rs565828460 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235818111 | TAACTTTAATCATTT[A/C]ATGATTATTTTCATG | 1130 |
rs565830244 | in-del | -/AG | | | intron-variant | LYST | GRCh38.p7 | 1:235852338 | TGTCAGGGAGGGAGA[-/AG]AGATTCCTGTACCTC | 1130 |
rs565832502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686647 | CTCTTACAGTATACT[A/C]CTAAGGATTCAGGTT | 1130 |
rs565837474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783087 | ATTTAGGAATGTTTT[A/G]AACTCCATTTTAAGA | 1130 |
rs565841786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745322 | ATTTTAAGTTTGTAC[A/G]TATATATTCATTAGC | 1130 |
rs565859045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235841609 | GAAGATACTGAAGAC[A/G]GGGGCAAGAGAACGA | 1130 |
rs565863969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827851 | ATTCTATTTACCATA[C/T]ATACAAAGAAAATAC | 1130 |
rs565871968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783911 | TTGAGACAGGGTCTC[A/G]CTCTGTCACCCAGGC | 1130 |
rs565889593 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753558 | CATCCATGAGCCCTT[C/T]ATGTCCAAAGAAACT | 1130 |
rs565915119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811964 | CCTCCTTAAAAAAAG[C/T]TCCATGAAATTCACT | 1130 |
rs565924221 | in-del | -/GTGT | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235750531 | AATACTCTGGAGATG[-/GTGT]GTGTGTGTGCATGTG | 1130 |
rs565932812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235712284 | TTACTTTTGCCACTT[C/T]AAAAAGATTAAAATA | 1130 |
rs565938750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819232 | CAAACACAATTCATC[A/T]TTGGGGAAGTTCTCT | 1130 |
rs565959853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680591 | TCTAATAAGGACACA[C/T]AAGTGATTTTCTTTT | 1130 |
rs565975931 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827089 | TATTAATAAGCTGGG[A/C/T]GCAGTGGCTCACACC | 1130 |
rs565990978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856837 | AACTCTAAGTCATAA[A/T]GCAGTAAAGGTACAA | 1130 |
rs565993899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712859 | AATTAAGTTTGGACT[C/G]TCTTTTCTGCCAACA | 1130 |
rs565996709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775942 | ATAAGTTTTAGACTT[A/C]AAAACATACTTTAAA | 1130 |
rs566012272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819991 | CAGGGAAAATAACTG[C/T]GTTACACCTTTATAA | 1130 |
rs566016293 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712668 | AGACTACTTTTTCTC[C/T]TTTCTTTTCTTTCTT | 1130 |
rs566019615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235679894 | GTTTCAGGATTGATA[A/G]TGTCCTCAGGGCTAA | 1130 |
rs566036590 | snp | C/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738748 | AAGGCTACACATCCT[C/G]GGCCATTGGACTCTC | 1130 |
rs566043461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235855796 | TAAATACACCTTGCA[C/T]GTATAGATAGCACGT | 1130 |
rs566046441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235703609 | CTTAGCTTTTCGTAT[A/G]TTTAATCAGTCATAG | 1130 |
rs566047075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753829 | TCAAATAAAGTAATG[C/T]ACAATTGTTTCGTGA | 1130 |
rs566050090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698441 | AAATGAGTATCTCTG[A/G]AAAAGCTTAAGAGCT | 1130 |
rs566084430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235684635 | TTTTAAAAACAATTT[C/G]AGTCAGGTCTCACTC | 1130 |
rs566089714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698821 | GAGCTTGCAGTAAGC[C/T]GAGATCACGCCACTG | 1130 |
rs566097128 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740511 | AGATGAATAGAATCA[C/T]AGATTGTACTCCTTT | 1130 |
rs566102490 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235692070 | GGGCACAGTGGCTCA[C/T]GCATGTAATCCCAGC | 1130 |
rs566107007 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235862695 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATC | 1130 |
rs566108483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678511 | ACCAGATGTCCACAC[A/G]GGGTTTGACTCTTGC | 1130 |
rs566137202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235721329 | ACAGTTACCATGTCT[A/G]TAATATGGGAGTGAT | 1130 |
rs566140923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796950 | TCATATCCACCAGGA[C/T]AGATATAATTAAAAA | 1130 |
rs566173994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729451 | CTCATATGCAATTAC[A/G]TATAATGTTAAGGCA | 1130 |
rs566213413 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235692742 | AAAAACGTTTACATG[A/G]GCCAGACACAGTGGC | 1130 |
rs566222250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790366 | CCTCTAAAAATACAG[A/C]TAGTATGAGCACTTA | 1130 |
rs566224345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798728 | AAAGCATCATGCTAT[C/G]TGAAAGAAACCAGTC | 1130 |
rs566224559 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695583 | CAAAGTGATAATACC[C/T]GCTCTTTCTCTTTTG | 1130 |
rs566235817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775220 | ATGCTCATACTCTAC[C/T]TATGTAAGGCTTGTG | 1130 |
rs566268441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879210 | ATGAGGTGAGTATCC[C/T]ACCCACTTGTGGCTG | 1130 |
rs566269862 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235878337 | GGTGGACTCTGTGAC[C/T]AGTGTGCAAGCTGCC | 1130 |
rs566287328 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235848919 | GACCAGACAGATTCA[C/T]GGCAGAATTCTACCA | 1130 |
rs566290096 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235804170 | ATCACCACCATCCCT[A/G]AATTAGCATTTAATA | 1130 |
rs566295381 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875483 | TTCTGACTCTCCAGA[A/G]TGGCTGGTGGAGAGT | 1130 |
rs566301652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871502 | ATTCTTAGTTTAAGA[C/T]TAGGTTTTGCTTTAA | 1130 |
rs566318926 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235780672 | AAGGAGATATAAATA[C/T]AAAGCCTGAAACAAA | 1130 |
rs566344833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235760644 | TACTGATACAGAATG[C/T]ATGAGAGAGGGGCCC | 1130 |
rs566351447 | snp | C/T | 9.93904e-05 | 0.00704878 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802923 | CATCATCCTGGGTTT[C/T]GCCATCTTCAGGATT | 1130 |
rs566353899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697768 | GGTTCTCATCTCAAA[C/T]AGATACGTGATGAGT | 1130 |
rs566356116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235788423 | AAACTCCTGACCTCA[A/G]GTGATCTGCCTGCCT | 1130 |
rs566363735 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661511 | GCCTAGGTATCACTA[C/T]ATGTGTATGCAGTTT | 1130 |
rs566368650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663282 | AGATGCTCATAAATG[C/T]GGTGATATAGAATAA | 1130 |
rs566381142 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662622 | ATCATAGAAAAAGGG[A/G]AGACCTTAATATTTT | 1130 |
rs566382913 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671780 | TCCTTATAGCCTGGC[A/G]TAGATATGTAAATGG | 1130 |
rs566404154 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235811028 | TGCACGCCTGTAATC[C/G]CAGCTACTTGGGAGC | 1130 |
rs566442063 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235782207 | TTTTGGAGACAGAGT[C/T]TCGCTCTGTTGCCCA | 1130 |
rs566450682 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885086 | TGCTCTTTTTAAATT[A/G]GCAATTATGCCAGGT | 1130 |
rs566452082 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827633 | ATGTTGATAAAGGCC[C/T]ATGTTTTAAATGGCT | 1130 |
rs566478013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796028 | TAAATAAAAGGTTGG[A/G]ATTGAAAAAATGTCT | 1130 |
rs566487889 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235773312 | AAAAGAGTAAAACTC[C/T]ATTTCAAAAAAAAAA | 1130 |
rs566507750 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235773787 | AAGATGGTAAATTTT[G/T]TGTTATATGCATTTT | 1130 |
rs566518083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744229 | TAAATAGTAATAATA[C/T]TGGTAAAAAATATTG | 1130 |
rs566524059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878334 | GCGGGTGGACTCTGT[A/G]ACCAGTGTGCAAGCT | 1130 |
rs566534078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696732 | GTTTGTTGCTTAAAC[C/T]CATGACTATATCTTC | 1130 |
rs566539731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677942 | TTTCTAATCTTGACA[C/T]TGTCTTCAAAATAAT | 1130 |
rs566566817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774712 | TACTTTTAAAAAATG[C/T]TTTAAAGAAAAGAAA | 1130 |
rs566571711 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235850320 | GAATAATCAGCTAGC[A/C]GCATGTAGGAGAATG | 1130 |
rs566596979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235781716 | CTAGATTACAAAAAC[A/G]TTAAAATATTTTAAA | 1130 |
rs566641807 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235703031 | TAAAAAGAAAGACTT[C/G]ACAATAATACCAAAG | 1130 |
rs566669138 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235838958 | ACTCATTCTCTCTCT[C/G]TCCCCCTACTGCCCT | 1130 |
rs566679919 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769988 | GATCAAGCTGTAAGA[C/T]GCAGCAGTTGAAAAA | 1130 |
rs566692686 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LYST | GRCh38.p7 | 1:235710777 | CTAAGAACAGGCTGG[A/G]AAAGGCCATGCAGCC | 1130 |
rs566712037 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235803830 | GTAACATAAAATGTT[A/G]TTTCAAAACCTTATA | 1130 |
rs566739109 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883532 | TACAACTTTCCCACG[A/T]AAGAATGAATAAACA | 1130 |
rs566750433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235846747 | TCTGGAAAGTCTCAG[C/T]GATAGAACTAAACAA | 1130 |
rs566755408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235816052 | GAAGAATCACTTGAA[A/C]CCGGGAGGAGGAAGA | 1130 |
rs566770352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235741784 | ACATATCCATACACA[C/T]AGGAGTTTAAAAGAG | 1130 |
rs566774825 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884068 | CAAGAGATCCTCCTG[C/T]CTCAGCCTCCCAAGT | 1130 |
rs566777616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235869311 | CCCCGTCTCTACTAA[A/C]AATACAAAAAATTAG | 1130 |
rs566777948 | snp | C/T | 9.90001e-05 | 0.00703493 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751354 | TAAGCTGTAGTGCAA[C/T]AGCCATATCTAAAAA | 1130 |
rs566785464 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235847597 | TGCTCCACTTAAAAG[A/G]TACAGAACCACAGAA | 1130 |
rs566816361 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235763193 | CCTTGAGGAAAGGAC[-/TG]TGTCTTTTATTTTTA | 1130 |
rs566826609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676226 | ATTGCTCTCTGTCTG[A/T]ACCTGGAAGACATAT | 1130 |
rs566862751 | snp | A/G | 4.94311e-05 | 0.00497123 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734508 | ATTTTAATAAGGTCT[A/G]CTTTTGTTGATGCAC | 1130 |
rs566878181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235800606 | GTATTAAAATTAAAT[A/G]CATTTTTAAAAATAT | 1130 |
rs566890626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235726713 | TAGCATGCAAGTTGA[C/T]TTAAAATTAAATGGT | 1130 |
rs566931107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235869901 | GATACAGTCCTGCTT[C/T]AAGGGCTTTGCACTG | 1130 |
rs566933941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710248 | CAAGGGTTTATATAA[A/G]TTCACATGGGATGGG | 1130 |
rs566943635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235708524 | TACTGTGCCTAAACT[A/G]TACAAACAATGCAGT | 1130 |
rs566956918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862454 | CTATAGTGTATATAG[A/G]ATTCAGTACTATCCA | 1130 |
rs566960330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851511 | CCACTAAATAACTTA[C/T]TCATGTAACCAAATA | 1130 |
rs566962289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860018 | TCTAATTACAAATCA[C/G]TAAGCACTTGGCAAG | 1130 |
rs566982898 | snp | A/G | 0.000183638 | 0.00958046 | intron-variant, nc-transcript-variant | LYST, MIR1537 | GRCh38.p7 | 1:235853016 | CAACTGTAACTAGAC[A/G]GTTTTCTGTGTGGAC | 1130 |
rs566994593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235816823 | ATAGGCCCTGGCAAA[A/G]GTTTCATGACGAAGG | 1130 |
rs567004126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235740854 | GTGACAAGTTAAATA[C/T]ATGTTTAATTTTTTA | 1130 |
rs567013949 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235875871 | AAACAAACTGCATTG[-/A]ATGTACTAAAGGCAT | 1130 |
rs567022946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725643 | TCATGCTTCCGAGTC[A/G]TTCAGCAAAGGGAAA | 1130 |
rs567033405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235675428 | GTGTTAGGGATAAAA[A/G]TCTTTATCTCCTTTT | 1130 |
rs567035455 | snp | G/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805921 | TCTTCCACATTTATG[G/T]AAGAAATATGCTGTA | 1130 |
rs567047032 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765906 | TGGCATTTAGACTCC[C/T]TGAGGACAGAGGCCA | 1130 |
rs567071460 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669669 | CATAAAGTGGCCAAT[A/G]GGAAACCTCCGCAGG | 1130 |
rs567078963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235689576 | TTCTGGAGATCTAAC[A/G]TAGAGGATGGTGACT | 1130 |
rs567082987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794807 | CATTAAAGGTTTTTA[A/C]GTAGGAAAATAATAT | 1130 |
rs567107746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756713 | ACCCTCATGGAGCTT[A/T]TATTTGTGAGAAATT | 1130 |
rs567109582 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684453 | GGGTTTAGAATCGAT[C/T]TGTAGGGGAAGTCAG | 1130 |
rs567140025 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235694013 | TCTCTTCTTCTTCTT[-/C]TTTTTTTTTTTTTTG | 1130 |
rs567141528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837590 | TGAGATTGAGCCACC[A/G]CATACCAGCCTGGGT | 1130 |
rs567151516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779882 | AAGAAGCAAGAGAAA[C/G]AGGAACCCAGTTTCA | 1130 |
rs567152475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235683229 | GAAAATAACTTCCAG[C/T]GGGTCGAGCAGGTCT | 1130 |
rs567185335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716207 | TAATGCGTAGCTATT[A/G]TGATTTTTGAATTTC | 1130 |
rs567202408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823366 | CTGCAGAACTAGATA[C/T]AGTAAATTAATGCTC | 1130 |
rs567214460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682471 | TGCAGCCTCAGGAAG[C/T]CCACAGCAGGCACTA | 1130 |
rs567273372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834873 | AGAGTCCTAACACAC[C/T]TTCCATACCTGTTCC | 1130 |
rs567279240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687808 | AACATGTTTCCCTGT[C/T]TTCTGATTCAGAGAA | 1130 |
rs567290156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235717631 | TCAACCTGCAGCACC[A/G]TAACTAGACCAACAG | 1130 |
rs567319368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673757 | TACCCCTTCCCCAAG[C/G]CCATCCAATCAAACC | 1130 |
rs567331298 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882451 | ATTAAGCTGGATATA[A/C/T]GCCCAAGCTTGCATT | 1130 |
rs567332271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235844895 | AATCTAAGCTTTACT[A/G]TGTAACTTTTTAGTC | 1130 |
rs567370938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757601 | TTTCCTAATTTAACT[A/G]TGATTAACAAATTTA | 1130 |
rs567386601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874523 | TTAAACACTCAGCAG[A/G]CTTTGAGCAGGCCAG | 1130 |
rs567389090 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718902 | AAAGTATCACTATGA[A/C]CTTACGTTTCTTTTT | 1130 |
rs567394668 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235879527 | GTTTGAAGGGAAAGA[A/G]AACAGGGAAAAATAT | 1130 |
rs567401550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701555 | ACTGTTTGAACCCGG[A/G]AGGCAGAGGTTGCAG | 1130 |
rs567416183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695127 | CCTCTCCCAGACCCT[A/C]GGGTATTTACAGGCC | 1130 |
rs567416274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793980 | TGGGACTACAGGCAC[A/G]TGTCACCATGCCCAG | 1130 |
rs567421680 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867477 | CGTCGGCTTCTTTCA[A/G]GAAACAAAAAGAGCT | 1130 |
rs567434791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235770967 | AAGATAACCTTCCCT[C/T]CATCTTATTATCCTA | 1130 |
rs567439936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763833 | TTTATCATCTCTCAA[A/C]TGGGTTACTATCACA | 1130 |
rs567452851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235873841 | CAAGGAAATTAAGAA[A/G]CATTATCATTTGAAA | 1130 |
rs567456804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813866 | TCAAGTTTGAGTTCT[C/T]GCCTTACACCAATCA | 1130 |
rs567476375 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235860678 | AGCCACTTTTAAACA[A/C]AACTTTACAGGTATA | 1130 |
rs567489952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814739 | AGGACATTCAGACTA[C/T]TCCTTCTGGTGTCCT | 1130 |
rs567490817 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235866986 | CCACCCCCTCCCTCC[A/C]CTCGTCCGGACCCAG | 1130 |
rs567496317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805670 | TACATATTACATTTT[A/T]TATATATATATGTGT | 1130 |
rs567503920 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235843717 | TGTATTTTCTGCTTT[G/T]TCCTTGTCTTGTGGC | 1130 |
rs567508523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707721 | AAATAACCATAGAAA[C/T]ATTAATTTTAATAGC | 1130 |
rs567529669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793003 | TCCCACTACAAAGTA[A/G]CTCCAAAGTTTTCTG | 1130 |
rs567532943 | snp | C/T | 3.30497e-05 | 0.00406494 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806150 | GTTTCTGTATTATCA[C/T]AAATATTAACTTATG | 1130 |
rs567538025 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841309 | GAAGGAGGCATAGGT[C/T]AAGGAATTTTTTTTT | 1130 |
rs567558874 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235674201 | TCCTTGGAAGCCTAA[A/C]AGGACGCAGTGAATC | 1130 |
rs567595682 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235771612 | TCTTTTTTTTTTAGA[A/T]CTGAAAGTATATATT | 1130 |
rs567627931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732512 | GATAGAATCACTAAA[A/C]TAGGATAACTGAAGC | 1130 |
rs567650547 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674954 | ATCATACCTTGTATT[C/T]GTGGATCAAGGCAAA | 1130 |
rs567663034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792285 | TTAAAACTTTCATTT[A/T]CTCGTAGCTGAGATA | 1130 |
rs567663860 | in-del | -/T | 0.418007 | 0.185132 | intron-variant | LYST | GRCh38.p7 | 1:235718194 | TAGTATAAATAGGGG[-/T]TTTTTTTTTTTGGAC | 1130 |
rs567666204 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794842 | AGTGTGTGTGCTTAC[-/T]TTTTTTTTCCAGTTC | 1130 |
rs567668386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799454 | CATCACCAGTAGTAA[C/G]ATCCAGATATCATAA | 1130 |
rs567697880 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235730570 | ATACATATTTATATG[-/TG]TGTGTGTGTGTGTGT | 1130 |
rs567721692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235775378 | AGTTTTTGATAAGTT[A/G]GTCAATAGACAGGCT | 1130 |
rs567722760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881857 | GGTCGCCAGAAGCTG[A/G]GGGATAGAAGGAAAT | 1130 |
rs567741137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235706759 | TAGCATTTATCTTCT[A/G]TTAGAATAATTAGGA | 1130 |
rs567758043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235731747 | TTTTTTAGTAGAGAT[A/G]GGGTTTCATCATGTC | 1130 |
rs567771426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740012 | TGAATTTTGATGGAT[A/G]GCAACTTTGCTGAGT | 1130 |
rs567783656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786487 | ATTGTGGAAGACAGT[A/G]TGGTGATTCTTCAAG | 1130 |
rs567807450 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235769645 | GATGATATCAATAAA[A/G]GCAGAGAAAAAAATT | 1130 |
rs567814848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235754067 | ATCAGCATTCTACCA[C/G]GGTCAAAACTCAGCA | 1130 |
rs567837520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235857671 | GGTGTGTCTGTGGGT[A/G]TGTGTGCGCGTGTGC | 1130 |
rs567847167 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235824487 | ACTGATGAGGACACT[A/G]TGCTCTGGAGCAATT | 1130 |
rs567857449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235692838 | CCAGCCTGGGCAACA[C/T]GGAGAAACCCTATCT | 1130 |
rs567872268 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708103 | ACCCAATGACTTGAA[C/T]AAATTTAAGATTATC | 1130 |
rs567879945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714562 | ATGATTCCTCAAAGT[A/T]TTCTGGATTCCATGA | 1130 |
rs567896285 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830151 | AGGCTTCAGAAACTA[C/T]GTAATCCAAAACCAT | 1130 |
rs567898467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857694 | GCGTGTGCACACAGG[C/T]GTATATATATACACA | 1130 |
rs567900752 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235748301 | TTAAGGGTGATGTGT[-/AA]AGTTTTTCATACTAA | 1130 |
rs567909434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235699543 | GCAATAAACATACGA[A/G]TGCATGTGTCTTTAG | 1130 |
rs567931424 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235744741 | CCCATCTCTACAAAA[A/T]AATACAAAAATTAGC | 1130 |
rs567932822 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809303 | CATAAAATGAGAATA[C/T]TCACATCGTCTGTGC | 1130 |
rs567962131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745224 | GTTACCACTTTTTTT[A/T]ATGTGTGATGAGAAC | 1130 |
rs567962712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235842545 | CACTGCTAAATCTCT[A/G]GCATCTAGAACAGAA | 1130 |
rs567977323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850568 | TGCATGGCAAAAGTA[A/G]CAGTCAGCAGAGTAA | 1130 |
rs567994626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742528 | ATATACTTAGTGCCA[C/T]TGAATGTATCCTTAA | 1130 |
rs568002482 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235731248 | TAAAAAAAATCATTA[C/T]AGAGATTGAGTAAGT | 1130 |
rs568024210 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235766611 | ACTCACTAGCCATGT[C/G]ATCTTAGGTAAGTTA | 1130 |
rs568024499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827003 | CTAACTGCATACACA[C/T]TATCTGTGCACTTAC | 1130 |
rs568051467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819926 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 1130 |
rs568063356 | in-del | -/GAG | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235736413 | ATGAATGGATAGAAT[-/GAG]GATATAGATAGACAA | 1130 |
rs568072971 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866034 | GGATGTTTTGCTATG[C/T]TTTGTTTAACCAGAT | 1130 |
rs568082351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872277 | CTCCAGCCCAGGCAA[C/T]GGAGTGACATTCTGT | 1130 |
rs568111973 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235861603 | ATTAGCTTATTTCCT[A/G]GTTCTTAAAGTGTAG | 1130 |
rs568135359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235865033 | ACAAGGCCTTATACA[A/G]TCTAATCTCCCACCA | 1130 |
rs568162818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864130 | CGATCCCCACACTGC[C/T]GCTTGGCTATAAATT | 1130 |
rs568192984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752815 | GGGTTAGAAACTAAC[A/T]TGGGCCAGTTAATAA | 1130 |
rs568193370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235855622 | GAGCCTTATCCTAAA[C/T]GTGAAATGAAAATAA | 1130 |
rs568204211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235840629 | TGAACAGTCAGGGCT[C/G]AGACTCACTGCTACA | 1130 |
rs568210448 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822610 | TATACTTCAAGAGGC[A/G]TAGAGGGGAGTGAGT | 1130 |
rs568234912 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793282 | GTAAAGAAAATATAA[C/T]CTCAGCGATATGTCT | 1130 |
rs568236743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738406 | CAAGTTGCTTATTGT[C/T]TCAAATCCAGTGGAT | 1130 |
rs568301827 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235790914 | GACATGGCATGAGAA[C/G]GAGAACTTGAAATAA | 1130 |
rs568312380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719479 | AATAATTGATTCAAG[C/T]AATAATCATCAATGG | 1130 |
rs568314203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235728433 | CTCAGTGCTAAATAA[A/C]TGTTGGCTATTTATT | 1130 |
rs568323480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235781207 | CTCAATTTCGAAATT[A/G]GTGTAACGAGAAAAT | 1130 |
rs568351085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727825 | GGAATGAACATAAAT[C/T]GATATAATAGGAGCA | 1130 |
rs568355879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832635 | TACTGCTACATGTAA[A/G]TATTACATATATAGC | 1130 |
rs568374907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235720282 | AACCAACTATAAAAA[A/G]CTATCTTTGAGAGAA | 1130 |
rs568387817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685944 | CTCAGTAAAACAGAT[G/T]TAATACTATAAAGAA | 1130 |
rs568390802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826446 | TACTAATCAGAAATT[A/T]AAAAGTAGTGAACTA | 1130 |
rs568393153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235833726 | TAATTTTAACAAAGT[C/T]GTGACATAATCAGTG | 1130 |
rs568394033 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235759930 | TAATGCTTAAAATTC[G/T]TAAATGCCAAAACTA | 1130 |
rs568412496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235797323 | AAAAGTAACTTTACA[A/G]TGGAGAGACCTGACA | 1130 |
rs568421220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235704267 | ATTCTTTTGGGTATA[C/T]ACCTAGTAAAGGGAT | 1130 |
rs568423969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863531 | TAATCAGATGAAGGT[A/G]TTCAAGTTAAATACA | 1130 |
rs568439685 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810332 | ATCTGAGGTGGAGAG[C/T]TGTGTCTTTCTTGCA | 1130 |
rs568445649 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707852 | TTGGAACCAGAATTG[C/T]TTTGGATTTCAGGGT | 1130 |
rs568476104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235810874 | AGAGGCTGGGTGAGG[C/T]GGCTTATGCCTGTAA | 1130 |
rs568480270 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYST | GRCh38.p7 | 1:235691010 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 1130 |
rs568481107 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235773267 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 1130 |
rs568481394 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735415 | TTAGCCAATCTTTTA[C/T]TAACAGGCCCTAAAA | 1130 |
rs568503546 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662574 | TATATAAACAATCAA[A/C]CAACCAATTTAAATT | 1130 |
rs568503645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235705074 | TGAATTTCCTTCCTC[A/G]TTTATGAGGTTGGTT | 1130 |
rs568516560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696654 | GGAGTCAGAAAAGGA[C/T]TGGTTTTCAGGAATA | 1130 |
rs568556162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848369 | TATCAAAACCTCTGC[A/G]ATGGAGCAAGGGTGG | 1130 |
rs568559530 | snp | C/G/T | 0.0131013 | 0.079955 | intron-variant | LYST | GRCh38.p7 | 1:235803963 | GAAACAAGCCAATTA[C/G/T]GTACCACATAATTTT | 1130 |
rs568559843 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235698597 | TTGAGAAAGGCCGGG[A/C]GCGGTGGCTCAAGCC | 1130 |
rs568560844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235877652 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 1130 |
rs568562871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235817218 | AAATGAAAAAAAGAA[A/G]AAAAAAACATGCTGG | 1130 |
rs568595326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235870027 | TCAATGAGGTCTACC[C/T]TTAATACTGCCCTTA | 1130 |
rs568608285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767071 | TCTTTCTACTGCACC[A/G]TTTACTGTCTGGAAT | 1130 |
rs568612236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697839 | TAGAGAATCTCTAGC[C/T]AGTACTAGAGAAGAA | 1130 |
rs568612430 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235670952 | GCAGATAATATGATT[C/G]CCTCTGATAACCCTC | 1130 |
rs568619265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235711000 | CTCCAGAAAACCTGA[A/G]GGCAACAGCATGAGA | 1130 |
rs568624210 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235770513 | GAATACAATATTGTA[C/T]TAGGTGCTTTCCTAC | 1130 |
rs568624748 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830811 | TTTAAAAATATAACC[C/T]ATTTTTCACTTGATA | 1130 |
rs568633878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235781464 | ACTGTCTGAATGCTA[C/T]TATGTGTGAGGTTTA | 1130 |
rs568638268 | snp | G/T | 3.32613e-05 | 0.00407793 | intron-variant | LYST | GRCh38.p7 | 1:235774017 | TTAGCATTAATATAA[G/T]ATGCATTAGTAATTG | 1130 |
rs568638791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831173 | AAGATATTTAACATA[C/G]AGATGTTAAGTTAAA | 1130 |
rs568641275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824975 | CAGTGAGCCAAGGTC[A/G]CGCCACTGCACTCCA | 1130 |
rs568641327 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235813471 | TTAAATGAAAAACTC[-/A]AGAGACGATTTTAAA | 1130 |
rs568642593 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235692365 | CAACCAACCAACCAA[A/C/T]CTAGCTGCTATCAGT | 1130 |
rs568670863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780511 | TTATAAGTATGGAAA[G/T]AAAATATAATGAGCA | 1130 |
rs568673960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878222 | TGAGCTCGGCCTTCA[C/G]CTGGAGGGGGACTCC | 1130 |
rs568684427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808308 | AATAAAGAGTAAATA[C/T]GATCACACTGCTGCC | 1130 |
rs568689029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766416 | TACTTACCATTACCA[A/T]AACAACTCATTAAAT | 1130 |
rs568708175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235870781 | ACAGTGCCTGGCACT[C/T]AGTAGGCACTCAGTA | 1130 |
rs568732653 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235664214 | GGGTAGATGTGGGAA[A/T]AAGAGAACTTTTAAC | 1130 |
rs568735610 | snp | C/T | 4.94376e-05 | 0.00497156 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787250 | AATCCTCCTTTTCCC[C/T]TGGGGCTGCTGTAAG | 1130 |
rs568747784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668847 | CGCAAACTTGTACTA[C/T]CAAAGTCAACTCTTT | 1130 |
rs568763800 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235802832 | CAAAATTCTAAAGTG[G/T]TATTATTATGAACCA | 1130 |
rs568778488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669439 | TTTCTGCTGGCAGAT[A/G]GGAAATTGGCTGTCT | 1130 |
rs568834562 | in-del | -/CACA | | | intron-variant | LYST | GRCh38.p7 | 1:235666267 | ACACACACACACACA[-/CACA]ATTTTCTTTAGCCGT | 1130 |
rs568836246 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235774524 | TGAAAAACTAACTCT[A/G]TAGCAGCAGTGCCTA | 1130 |
rs568910125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751079 | GGAGCAGAATAGTTT[C/T]CTTCAGGAAAAAATC | 1130 |
rs568931391 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235690778 | GTTATGCAGGTAATG[C/G]AAATCAGAGGATGAA | 1130 |
rs568944018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743625 | AATTAGAAAAATGAG[A/C]GTAAGTAGCCATAAA | 1130 |
rs568972369 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235788175 | TTTATTTATTTATTT[A/T]TTGAGACAGAGTCTC | 1130 |
rs568984555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765411 | GCAATAATTTACTTA[G/T]AGCCTTTGCTCAAAA | 1130 |
rs569010532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235668185 | AAAGGATTGTCTGTA[C/T]GTATATACATACATA | 1130 |
rs569020764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235675336 | TAGTTAGAAAACTTT[A/T]AGTCTTAGCCAATTG | 1130 |
rs569038150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852890 | GCAGAGTCCTATCCA[A/G]TGTTTTTCCTAATAC | 1130 |
rs569073014 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235846034 | CAGGAGGCCAACCAG[C/T]ACAAAAATAGAGCAT | 1130 |
rs569088140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235718321 | ACATGTTGGTCTATA[C/T]ACACCCAGATGTTTT | 1130 |
rs569101190 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235837464 | GAAATCCCATCTCTA[A/C]TAAAAATACAAAAAT | 1130 |
rs569115004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235860986 | GGCTTTTTTTCGTGC[C/T]GTGTAATTATTTTGA | 1130 |
rs569152873 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883356 | AGCTGACTTAGGGTA[A/G]GATTATTCCCCTGGC | 1130 |
rs569156412 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660686 | CCATCCTGGCTAACA[C/T]GGTGAAGCCCCGTCT | 1130 |
rs569174091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702327 | ATAAACCAAAACATC[C/T]GCATCACTGGTCAAT | 1130 |
rs569185428 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235800470 | TAATAAATTCTATGA[C/T]AGGGTATCTACTATA | 1130 |
rs569190471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758376 | GACTCTGTGCAGTCT[A/G]GTGACAGCCTGTCCT | 1130 |
rs569191048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875777 | TGAGCCCAGGAGTTT[A/G]AGGCTTGCAGTGAGG | 1130 |
rs569205934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235682426 | AGCCCCAGAGAAGCA[C/T]GTGGCGGACAAGCAA | 1130 |
rs569221154 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235829428 | AACATTCAAAGTGTT[-/A]AAAAAAAATCCATCA | 1130 |
rs569235662 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235831215 | TTGCCTCACCTCCCT[C/T]CACCCGCTTCAGGGG | 1130 |
rs569252088 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235785592 | AAAGCACCTAGCAAA[A/C]GGTCTGCAACATAGT | 1130 |
rs569259751 | snp | A/C | 1.65061e-05 | 0.00287277 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734437 | TCAATCATTCTTTAT[A/C]TATGATGGAATCTCC | 1130 |
rs569279301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772576 | CCCTGACTGGGTCCT[C/T]GTGAAGACAAGCCCA | 1130 |
rs569283549 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858012 | TCAGCCATCTCCATT[G/T]ACTGAGAATTTTGTC | 1130 |
rs569306287 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235844841 | CAGTTAAAACATATC[A/G]GTTGAACTGTACAAT | 1130 |
rs569325628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717372 | GTAGAGTATGTATGC[A/G]TGCGTACAAATCTGT | 1130 |
rs569344926 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868650 | TTTGTAAAAGGCACA[A/G]AGTAATGCCATTTGT | 1130 |
rs569355763 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867356 | GGTCTAGAGGATGAA[C/G]ATAGAAGAAATAACG | 1130 |
rs569366396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801418 | TCAAACTTTCTGACC[C/G]CCCCCTCAAATACCT | 1130 |
rs569369262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235823710 | GTTTTCTCTAGCCCC[C/T]GTGTTTTTTCATGTG | 1130 |
rs569374316 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235723068 | AGAGCCAACAGAACC[C/T]ATTAATAGAGTGTAT | 1130 |
rs569377328 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235860254 | AGAGTTTCCATGTAC[A/T]CCCTGCTCTCTCACA | 1130 |
rs569388699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756548 | GTTGTATTGCAAGTG[A/T]TTAAACAATACCTAC | 1130 |
rs569392984 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235858870 | GGGGGCAGGGAAGGG[C/G]AGTGGGAGCAGGCAG | 1130 |
rs569394455 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727230 | TGGGTTCAAGCGATT[C/T]GCCTGCCTCAGCCTC | 1130 |
rs569413983 | snp | C/G | 0.000183479 | 0.00957631 | intron-variant | LYST | GRCh38.p7 | 1:235733463 | ATCAATATCTTAAAT[C/G]TTCATGGAAGACAAT | 1130 |
rs569435716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235682093 | AGGCAGGAGGATTGT[C/T]GAGCCCAGGAGCTCG | 1130 |
rs569478303 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235694550 | ATACCCAGAAGTAGA[A/T]GAGTATAACAAATAA | 1130 |
rs569482960 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235782344 | GGTTAATTTTTTGTA[-/T]TTTTTTTTTTAGTAA | 1130 |
rs569491698 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235882783 | GATGTTCAGTTTCAT[C/G]TGCCTTGTGTAAAAA | 1130 |
rs569497153 | snp | C/T | 1.7789e-05 | 0.00298231 | intron-variant | LYST | GRCh38.p7 | 1:235741636 | CTTGAACCCTAAAAT[C/T]AATCAAGATAGGAAT | 1130 |
rs569503297 | snp | C/T | 5.97663e-05 | 0.00546622 | intron-variant | LYST | GRCh38.p7 | 1:235762902 | TTAAAAAGGATAAAA[C/T]GAAAATATAACTTTA | 1130 |
rs569504100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723035 | GAAGCAGTCAGACTC[C/T]CGATGTATTCTGAGG | 1130 |
rs569504492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732423 | TCCTCCCGCCTCAGC[A/C]TCCCAAAGTACTAGA | 1130 |
rs569523376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690058 | ATGCCTAGTAATTAA[A/T]GGTGTAAAGAATTTG | 1130 |
rs569576330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794619 | GAGATAAGTTTTAAA[A/G]GACTGGTAGTTTTGG | 1130 |
rs569586922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666305 | AGGAATGAAGCATGC[A/G]AAAACATGGATGAAC | 1130 |
rs569593551 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235836884 | AAATTAAGTAATCAA[C/G]TAGGCAGCTGAAGAT | 1130 |
rs569593687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829508 | AGTTCCCTGAAAGCA[C/G]ATTGTAGAGTTTTAC | 1130 |
rs569620502 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235755295 | TCAGGAGGTTGAGGC[A/T]GGAGAATCGCTTGAA | 1130 |
rs569621526 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235866909 | CCGAGCCGACGCCGC[C/T]GCCGCCGCCGCCGCG | 1130 |
rs569642685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235813769 | AGGAGCAGTCATTAT[C/T]AGAAGTATGGAAGGA | 1130 |
rs569669312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851323 | AAACAAAACATCATA[C/T]GTTCTCACTGATATG | 1130 |
rs569680973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699540 | GCTGCAATAAACATA[C/T]GAGTGCATGTGTCTT | 1130 |
rs569686258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235800585 | ATTTTTCAAAACAGC[A/G]AGCATGTATTAAAAT | 1130 |
rs569743862 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235786006 | TATCACCTTATACAT[A/G]GGCTAGTCATTCTAA | 1130 |
rs569746998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763656 | GAGAGACGAGGTTTC[A/G]CTATGTTGACCAGGC | 1130 |
rs569756330 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235762027 | TGCCTAATGCTAAAT[A/G]ACGAGTTAATGGGTG | 1130 |
rs569761089 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235841702 | GAGGTTAGGCTGGGG[C/T]GGGGAAGCAGGAGGG | 1130 |
rs569784842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881650 | ATATATTTACATACA[C/T]GTACATACATATATA | 1130 |
rs569792251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827908 | TCCAGAATACATAAA[G/T]AACTGCTACAACTGA | 1130 |
rs569800160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235776692 | AAACAAATTAAAGTT[G/T]TTTTTTTTTTAAAGT | 1130 |
rs569810776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235700233 | GAGCCAAAATTGACA[A/C]CTGGGATCTAATTAA | 1130 |
rs569819709 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235873723 | CCCAATATATTCCTG[C/T]GGTCTACAAATTTCT | 1130 |
rs569826880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881008 | GAGGGTGCATGTAAT[C/T]CCAGCTACTCAGGAG | 1130 |
rs569829489 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718143 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 1130 |
rs569833329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784686 | GGATTAAATCAGGTA[A/G]TCTGTATAAAGTGCC | 1130 |
rs569836310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834720 | AAAAACATCCCTTCC[C/T]GATGGGTGCAGCTCC | 1130 |
rs569849984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828410 | GTACACATAAAATGG[G/T]TGAATTTTAAGATAT | 1130 |
rs569851858 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235679168 | TGAAAACAATCACAG[C/T]GACCAGATCAGCTTT | 1130 |
rs569852139 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235725515 | GCCTGGAGCCTAGAG[C/T]ATAGAAAAAAAGCCT | 1130 |
rs569866611 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713570 | CCAGGGGTTATTTGG[C/T]AATGTCTAGCAACAT | 1130 |
rs569870977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235783967 | TCACTGTAGCCTTGA[C/T]TTACTGGGCTCAGGT | 1130 |
rs569887625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235811402 | AATTATTTCAAAATC[A/C]TACACTATATGCCAA | 1130 |
rs569913288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701992 | CTTTTCCTCTTAAAA[C/T]AGGTCACAGATTACT | 1130 |
rs569930396 | in-del | -/CTTTT | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235777410 | CACACTCAACTGATC[-/CTTTT]CTTTGTTTAAAAAAC | 1130 |
rs569932186 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235717181 | CGGTGTAGAATGAAG[A/G]GCAGTTTCGACAGAA | 1130 |
rs569932222 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235820481 | CTCAGGCGATCCTCC[C/T]GCCCCAGCCTCCCAA | 1130 |
rs569939246 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875787 | AGTTTGAGGCTTGCA[A/G]TGAGGTATGGTACTC | 1130 |
rs569975204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672926 | CTTTACTCACTCCCT[C/G]AAGACTCAAAGCCTC | 1130 |
rs569994912 | snp | A/C/G | 0.000130138 | 0.00806558 | intron-variant | LYST | GRCh38.p7 | 1:235777342 | CATTCAGTAATGACA[A/C/G]CAAGTTTAAAATGCA | 1130 |
rs569995403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849725 | CTATACACCAACAGC[A/G]ACCAAGTGGAGAATC | 1130 |
rs569999844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693139 | GCTAACACGATGAAA[A/T]CCCGTCTCTACTAAA | 1130 |
rs570029997 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674638 | ATGCCATTAAAGGAA[C/T]AGCTGAACAATTAGG | 1130 |
rs570037351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235687682 | CCTGAGCACCATGTC[C/T]GCAGCAACTGTCCCC | 1130 |
rs570044195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235791197 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 1130 |
rs570047610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235798971 | CAAAACACTGAACTA[C/T]ACACTTTAAATAGGT | 1130 |
rs570058298 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872401 | CTGCTTAGATTCAAT[A/G]AAGAATGGACAGCAC | 1130 |
rs570079130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693765 | AATTATTATAAAAGA[C/T]AGTAATAGTGAAGCT | 1130 |
rs570079962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782232 | TGCCCAGGTTGGCAC[C/G]ATCTCAGCTCACTGC | 1130 |
rs570089729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235677982 | TGTTATAATATTCTA[C/T]ACAGTTAGTACCCCA | 1130 |
rs570091171 | snp | C/T | 4.87829e-05 | 0.00493853 | intron-variant | LYST | GRCh38.p7 | 1:235792163 | GAAACTTTCTAATCA[C/T]GTAATAAAGTACATA | 1130 |
rs570110979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768911 | CTAATTTACCACAGG[A/G]GCCAAGAAAGGCAAT | 1130 |
rs570134531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738655 | TGCACCCAGATTTAG[G/T]GACTGACATAGATAA | 1130 |
rs570149808 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820823 | TCTAATATATGTGTA[C/T]ATACACATATATGAA | 1130 |
rs570173240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722202 | ACAGCAGACAATGAC[A/G]TCAGAGAGGTAACAA | 1130 |
rs570180663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686765 | AAATGGGACTACTAC[A/G]ATTGTTTTCAAGATT | 1130 |
rs570217974 | snp | C/T | 0.000557258 | 0.0166829 | intron-variant, nc-transcript-variant | LYST, MIR1537 | GRCh38.p7 | 1:235853044 | GACAGGACAGAAAAC[C/T]GACTAATTACAGCTG | 1130 |
rs570225134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761080 | GCAAAAAGGCAAAAC[A/C]CTATCTCATTTATTT | 1130 |
rs570233870 | snp | G/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854796 | AGCATCCTTAGACCT[G/T]CAACTCCTCTCTTAC | 1130 |
rs570256868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235664369 | TTAAATCTCTAAATA[C/T]TGAATATTAATATGC | 1130 |
rs570264915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663383 | TTACATAAACAACAA[A/G]TATTTGGGTGTACAA | 1130 |
rs570299390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235856936 | AGTTACACAGGATAT[A/G]CTGATTTTTTTTTTT | 1130 |
rs570335364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849134 | CAAAATACTAGCTAA[A/C]CAAATCCAAGAACAT | 1130 |
rs570350296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235753880 | ATGAAAAGTAGCATT[A/G]AAACTACCATAACAA | 1130 |
rs570355759 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845532 | CTCGCAGACTTCACA[G/T]GTGGAAGGAAGAACT | 1130 |
rs570386061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761535 | GAGGGTATTGATTCT[A/G]AACATACCTAAAAAT | 1130 |
rs570389844 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235774061 | TTCAACAGAAACATT[A/G]AGCTTTCAATTTTAG | 1130 |
rs570389934 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817478 | CTAAATACCCATCAA[C/T]GGTAGACTGGATAAA | 1130 |
rs570432522 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235705814 | TTTTTATTTTTTATA[A/C]AGGGTCTCACTCTGT | 1130 |
rs570451023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775795 | AGTTCACAGTACATC[G/T]AGGAAGCTGCAGGTT | 1130 |
rs570460363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879396 | CAGGGAGCATATGGC[A/G]GGAATGGTCGCCTGC | 1130 |
rs570472401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766297 | AAAAATAAAAAAAAC[G/T]CTCTTTAGATTTAAA | 1130 |
rs570480912 | in-del | -/T | 0.452597 | 0.146474 | intron-variant | LYST | GRCh38.p7 | 1:235731557 | ATTTCCCATTTTGCA[-/T]TTTTTTTTTTTTTTT | 1130 |
rs570517078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768062 | GTAAACCTCAGTCCT[C/G]TGATTCTCTCACTAC | 1130 |
rs570517956 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235678163 | AAGAAATACTTCTGT[-/A]AAAAAAAAATTCTGG | 1130 |
rs570540957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235870718 | AGACTATGGGCTCCA[C/T]AAGGGCCACAATCTT | 1130 |
rs570555669 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235668296 | TGATAACTTTCTTTC[C/T]TTCTTGGCCTACAAG | 1130 |
rs570556193 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870321 | ATAGCCCACACCTGT[A/G]TCAATCCCTGAGTTT | 1130 |
rs570596922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235759884 | AGACTCCAAGCAGCT[A/G]GGACTATAGGCATGC | 1130 |
rs570603705 | in-del | -/TTT | 0.484771 | 0.0859212 | intron-variant | LYST | GRCh38.p7 | 1:235695630 | TTTACAGTACTCTAA[-/TTT]TTTTTTTTTTTTTTT | 1130 |
rs570620806 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235745060 | TCCATTTTGACTTAT[A/C]TATAGTGTTTTTTAA | 1130 |
rs570623977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235697817 | CTATGGAACATATTG[C/T]GAGGATTAGAGAATC | 1130 |
rs570636993 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759204 | ACTCATCCCCAGGAC[C/T]GTCATCTTCTGACCT | 1130 |
rs570638463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848307 | AAAACGAAATCAAGA[C/T]AGAAATTAAAAAATT | 1130 |
rs570638798 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739030 | CTGTCTAGGCTACAA[C/T]AGGATTTTAGTTGGA | 1130 |
rs570639063 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707614 | GGTGACAGAGCAAGG[C/T]TCCATCTCAAAAATA | 1130 |
rs570639590 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821350 | GCTGAGGTGGGAGGA[C/T]TGCTTGCGCCTGGGA | 1130 |
rs570644277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235692534 | TACAGGAATGTGCCA[C/T]CATGCCTGGCTAATT | 1130 |
rs570664139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704121 | AAAGTATTCCATGGT[A/G]TATATATACCACATT | 1130 |
rs570673702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751952 | TTGTGCTCAAATAAC[A/G]GGTTTGTCTGTTATA | 1130 |
rs570676148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235817052 | GGCCCTATTAAAAAG[C/T]GGCCAAAGGACACGA | 1130 |
rs570678758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831801 | TGGTTCTTTATATGC[C/T]TTCAGAAAGTAAAAG | 1130 |
rs570700990 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235863105 | CTTAAAAAAAATCTT[A/G]AACTTGGCCCAGCAC | 1130 |
rs570701317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736224 | TTTCAGCCCTTAAAA[A/T]ACTGATTTAAGGAAT | 1130 |
rs570703278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235726840 | TCAAATGGAGTTAAA[C/T]ACAAATTGAGTAGAA | 1130 |
rs570706063 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235847683 | ATAAGCACTCACATA[C/G]GGTAAAGGGGTGGGA | 1130 |
rs570711772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235685421 | TGCTGACTGGATCAT[A/G]TAACTCCTGTTTATA | 1130 |
rs570726373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744325 | CAATGTAGTAGAAAG[C/T]GAATTTACGTAAAAT | 1130 |
rs570740458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235735414 | TTTAGCCAATCTTTT[A/G]TTAACAGGCCCTAAA | 1130 |
rs570749755 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235692161 | AACATGGTGAAACCC[C/T]GTCCCTACTAAAAAT | 1130 |
rs570763017 | snp | A/G | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827329 | AGCCATGATTGTGCC[A/G]CTGCAGTCCAGCCTG | 1130 |
rs570766460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727722 | TTATTTAATATTTTT[C/G]CTTTCTTTCTGAAGG | 1130 |
rs570769389 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235729113 | TAATTGTTTTCCTTC[A/G]TATTTTGAGAATAAA | 1130 |
rs570787325 | in-del | -/TATACA | | | intron-variant | LYST | GRCh38.p7 | 1:235730505 | CAAAATATGTGTGTG[-/TATACA]TATACATATATATGG | 1130 |
rs570789648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669395 | GAACAAAAGGACCAG[A/C]GGCTACTCCCTTTGC | 1130 |
rs570797302 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693267 | CTTGCAGTGAGCCAA[A/G]ATGTGTCACTGCGCT | 1130 |
rs570820857 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769164 | AAGGGCAGGGAAGGT[A/G]TCTCTCAGGAAGTAA | 1130 |
rs570830915 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235817086 | GACACTTTTCAAAAG[A/T]AGACATACATGCGCC | 1130 |
rs570842747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719357 | CCATATTAGTTTCCT[C/T]GCTTTCTGACACAAC | 1130 |
rs570891213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235863489 | ATGTTGAACTTAAGC[C/T]GGCAACCAGATAATT | 1130 |
rs570932193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854628 | CAACTGAGTTCATAA[C/G]AGTAGCTGTAGTTGT | 1130 |
rs570935899 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884248 | TGCCTCAGCCTCCCG[A/C]GTAGCTGGGACTACA | 1130 |
rs570955484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845278 | CTGAGCTGAATCAAG[G/T]TAGAGAGCCAAGCCT | 1130 |
rs570996429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845879 | CACCTAGCCCCACCC[C/T]CACCTGATGGTCCTT | 1130 |
rs571007616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683314 | GTATAAGCTGCACAC[A/G]TATTCTTCTGCCACT | 1130 |
rs571028682 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235787928 | AAAGACCTGTATCTA[C/T]ACTACTTAATAAAGG | 1130 |
rs571033834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235668950 | TAAGACTAGCAAAAA[A/T]TCTTTCATATCTGAA | 1130 |
rs571064995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235787018 | AAACCTGCACATTGT[A/G]CACATGTACCCTAGA | 1130 |
rs571078227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814821 | ACCCCTTTTTAGGTA[C/T]AGAAAACCCTTCACG | 1130 |
rs571078852 | in-del | -/A/AA | 0.162581 | 0.234218 | intron-variant | LYST | GRCh38.p7 | 1:235877855 | ACAATATCTGCCACC[-/A/AA]AAAAAAAAAAAAAAA | 1130 |
rs571093457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235773511 | TACAACACAGATGAG[C/T]CTTGAAGACATTAAG | 1130 |
rs571101438 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235883137 | CTGCCCTCCTAAGCT[G/T]CCCATGCTCTCGGCT | 1130 |
rs571119568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831108 | AAGGAGTTTCAAAAT[A/C]GTTTCATCTCTGGGC | 1130 |
rs571134152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235676857 | TCAAATGCAATTTTA[C/T]ATGTATCAGGAAAAT | 1130 |
rs571156803 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235780416 | CTCTTAAAAAAAAAA[A/T]TAAAAAATAAAAAAG | 1130 |
rs571174562 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235802183 | TGGGCGACAGAGCAA[G/T]ACTCCATTTCAAAAA | 1130 |
rs571183120 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235726909 | AAAAGTTGTCTCATA[C/T]ATCAACTATTAAATT | 1130 |
rs571200039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235676302 | TTAAATAAAATTTAC[A/G]GGAGGCCAATGTTTT | 1130 |
rs571203670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802683 | GGGACTCTGTCCTTC[A/C]CTCCATGTTCTTAAC | 1130 |
rs571243700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235794931 | ACTACTGAAAACTCA[G/T]AGCATTAAAGTACAG | 1130 |
rs571247059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709358 | CCCACAGCAAGTTTC[A/C]TTCAGCTACAGAGCA | 1130 |
rs571257328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681343 | GGAAGAAACGTGGTG[A/G]TGAGGTAGAGGGGGC | 1130 |
rs571276135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785528 | TATATGTTATTTCCA[C/T]GGTCTAATCTACTTT | 1130 |
rs571279568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690318 | ATTTATAATAATCCC[A/T]AAAAGGGTGCAGTAA | 1130 |
rs571310508 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722405 | GAGCAGAGAAATGGT[A/G]GTGAAGGGACTGGAG | 1130 |
rs571328496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235750055 | TTTCTGATATCAAGA[A/G]AGGGCAAATTCCATC | 1130 |
rs571348097 | in-del | -/GA | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235840240 | CACTTAACCCAATTT[-/GA]GTGGCCAGGGAAGCT | 1130 |
rs571382849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235772518 | CCTATACTATTAAGA[C/T]TGCTTAAAACTAGGG | 1130 |
rs571410979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795345 | GCTACTGAGTGTAAC[C/T]GTACAGTCTGCAGAC | 1130 |
rs571412222 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682098 | GGAGGATTGTTGAGC[C/G]CAGGAGCTCGAGAAT | 1130 |
rs571423551 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235860105 | CTGGACTTTACCTTC[A/C]TCTCCCCCCATTTTT | 1130 |
rs571428459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763877 | TATCCTTGATGAGCA[A/T]CTCATTACTCTCAAA | 1130 |
rs571437317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235725363 | CACCTGAACCCAGGA[A/G]GCGGAGGTTTTGGTG | 1130 |
rs571446595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682048 | TTAACATGTGGCTCA[C/T]GTCTGTAATGCAAGC | 1130 |
rs571460292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235852227 | GACCCTACAGAATCT[C/T]AGTAACAACTCATGC | 1130 |
rs571507792 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801038 | GAGTGAGGTTTTCGA[A/G]TAAGTCATTTGGACT | 1130 |
rs571511743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235836166 | ATACACAAACACTGA[C/T]TTAATGTATTAGCTA | 1130 |
rs571530257 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235795559 | GTATGCAAACTGCCA[C/T]GTAGGGTAATAGTAT | 1130 |
rs571551052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757698 | TGATGTCTAATACAG[C/T]AGTCACTGTCACTTA | 1130 |
rs571571121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882596 | CCCCAGCTGAGGGTA[C/T]TGGAAATGGAGAAAG | 1130 |
rs571589187 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | LYST | GRCh38.p7 | 1:235764500 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 1130 |
rs571596212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235881945 | GAAATGGATAGTGGT[A/G]GTGGTTACACAAGAA | 1130 |
rs571596680 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235831013 | GGAAATAAGCTACAG[A/C]AAACAGAATAGGGGA | 1130 |
rs571624116 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235784855 | GCTACAGCTGCCATG[A/G]CAGCTATGAAGATCG | 1130 |
rs571625897 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235695027 | ATCTGTAAGCTACAA[A/C]ATTGTTCAGTCAATG | 1130 |
rs571639303 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830748 | ATAAAAATAAACCCA[C/T]TACTTATAAAATGTT | 1130 |
rs571649782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771785 | GGCTGCATACTCTTG[A/C]ATTGCCTCTTCATGT | 1130 |
rs571652143 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765841 | CTTACCAAATACACA[-/T]TTTTTTTTTTTTACT | 1130 |
rs571655166 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829249 | GAAAATTCCATGACA[A/T]GTAAATGCTTCCTAA | 1130 |
rs571661121 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235704636 | TGTTTAAGTTCCTTA[C/T]AGATGCTGGATATTA | 1130 |
rs571682548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778308 | GGCTTAGGGAAATCA[G/T]ATAGATTCAGTGTCT | 1130 |
rs571682754 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882823 | TGAGTCCATCTGCAC[A/T]CATGTATTGAGTGAG | 1130 |
rs571696483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235732651 | AAATTTTTGTTAACA[C/T]AAAAAGTAAAATGTG | 1130 |
rs571701956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798514 | ACCTGGGAGGTGGAG[G/T]TTGCAGTGAGCTGAG | 1130 |
rs571723043 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702050 | ATCTTTAAGGTCCTT[C/T]ACAACGTCTTTCCCT | 1130 |
rs571728370 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806673 | GCTGATTATCAGAGT[C/T]TCAAATGCTTTTAGA | 1130 |
rs571746241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829905 | CATCATGTTTCTGAC[A/G]TAAGATACAGGGATA | 1130 |
rs571771071 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235756169 | TCTTAAATGCAACAC[A/G]TGTAATACCAAATTA | 1130 |
rs571804859 | in-del | -/AATG | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868479 | ACACCCCCCTTTTTT[-/AATG]GACAAAAGAAGTCAA | 1130 |
rs571888268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235871101 | CATATACATCTTTTA[C/T]AATTGTGCGTCTTGG | 1130 |
rs571890293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235879759 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 1130 |
rs571895534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694465 | TAAATGGTACTGCCC[C/T]TGAAACTTGCAATGT | 1130 |
rs571900218 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235850879 | ATCAAAAAACAGTAG[A/G]TGTTGGCATGGACGT | 1130 |
rs571931726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835390 | ATCTATCTTGCAATG[C/T]TAAGATGATTCCAGC | 1130 |
rs571936710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740123 | GGAAGACAGTGCCCT[C/G]AGTGTACTTGAAAGT | 1130 |
rs571938125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235865287 | TGCCTCTAGTTAAAA[C/T]TGCAAACCTCTCCCG | 1130 |
rs571953988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801274 | GGAAATTTTGAAGAT[G/T]AATGAGTTCCCTTAA | 1130 |
rs571957157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843855 | AGTAACACCCAAAAG[A/C]CTTGTTAGTCTTTCA | 1130 |
rs571957167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235851255 | AACAGCATCTGCAGT[A/G]ACCTGGATGAGACTG | 1130 |
rs571967848 | in-del | -/TCAA | 0.0387552 | 0.1337 | intron-variant | LYST | GRCh38.p7 | 1:235701624 | AGAGCGAGACTCATC[-/TCAA]TCAATCAATCAATCA | 1130 |
rs571976672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235805075 | AGGAAGAGCCTGTTG[A/G]CTGACTGAACAGTTA | 1130 |
rs571979881 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859523 | TTTTTTTTAAATGTA[C/T]CTATATCTGACTCAG | 1130 |
rs571982885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698647 | GAGGCCGAGGCGGGC[A/G]GATCATGAAGTCAGG | 1130 |
rs571991936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844759 | CTGGTGGGGGGAAGG[G/T]GACCAAAGAGGGGGA | 1130 |
rs571998580 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673149 | CTGCCCTCTTCAAAG[C/T]CATGGACCACTGTCC | 1130 |
rs572005443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856266 | CTATGATGCACAGAC[A/C]TCTTTTGGTTATGAG | 1130 |
rs572006752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761223 | AAACAAAACTAGAGA[C/T]TAATACCTATATATC | 1130 |
rs572008680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235769191 | GTAAGTCTTAAGTTG[C/T]CACGTGGAGGATAAG | 1130 |
rs572032259 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739553 | TACATATAAACAATG[C/T]AACCAACTATCCAAG | 1130 |
rs572035679 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235879864 | GCCTTAGCCTCCCAA[A/G]TAGCTGGGATTATGG | 1130 |
rs572047441 | snp | C/T | 0.000136586 | 0.00826284 | intron-variant | LYST | GRCh38.p7 | 1:235663106 | AAAAATTCCCATTTG[C/T]ACATTATATTTCTTA | 1130 |
rs572048910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235706198 | TTAGGACACACAACC[A/C]CAAAATTTCGTACCC | 1130 |
rs572055251 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235745978 | ATCGATGTTACTCAC[A/C]TGGTGATGATATTAT | 1130 |
rs572069054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235754172 | GGCGTTCCTATATGG[A/G]TCCTTTATGTAATCT | 1130 |
rs572084908 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235699146 | TGTGCAGAACGTGCA[C/G]GTTTGTTACATAGGT | 1130 |
rs572086480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235714190 | AGGATGGCTTAAACA[A/T]TGGTTTTAAAAACTC | 1130 |
rs572121176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745557 | CGTATGACCCAGTAA[C/G]TGCACTCCTGGGCAC | 1130 |
rs572121738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775449 | ATGATACTTGTTCCC[A/C]ATGGGGTCTACTGTC | 1130 |
rs572143539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235693035 | TTAAAAAAAAAGTTG[C/G]CCAGGTGTGGTGGCT | 1130 |
rs572148706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736964 | TTTAGAACCATGTAG[A/G]CATTTCACATGATTA | 1130 |
rs572148951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235744553 | GATAATCATGGTTCA[A/G]TTTCAGAGTTTAGTC | 1130 |
rs572216829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235749395 | CAGAATTTCAATAAG[A/G]GTAGTACTTAAAACA | 1130 |
rs572227114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235818968 | GCTTCTCCTCCCACA[C/T]GAACCCAAGATTGCT | 1130 |
rs572235430 | snp | C/T | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720905 | ATACATCATCACGAA[C/T]CTAAAAGGGAAGGAG | 1130 |
rs572241985 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235708482 | TTCAGGAGAGGTCCT[A/G]CCATTCCCTAACTGA | 1130 |
rs572249400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235878809 | TTGTTGGAAACCTGG[A/C]TTTTAACCCATGCTT | 1130 |
rs572258313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712706 | TTTCGGGGGGGTGCG[C/T]AGGTTACGGTGCATT | 1130 |
rs572258984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864676 | GTGGCTCACGCCTAC[A/C]ATCGCAGAATGTTGA | 1130 |
rs572284650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235686089 | AAACAAAAACAGGCC[A/G]GGCGTGATGGCTCAC | 1130 |
rs572284792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235678245 | AGATCATGAGGTCAG[A/G]AGGTCGAGACCAGCC | 1130 |
rs572289055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235671067 | TAAACTATTTATTTT[C/T]ACAAGGATTACAGGC | 1130 |
rs572322820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235713204 | AAGGTTTAGAAACAT[C/T]TACTTTTTCTCAGAA | 1130 |
rs572335806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235692266 | TGAATCCGGGAGGCG[A/G]AGGTTGCAGTGGGCA | 1130 |
rs572339543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235711222 | AGAGAAAACAAGGAG[G/T]AGATTTAAACAGGAG | 1130 |
rs572345842 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870871 | AACAGTAAGTTGACC[A/G]TAATTTTGGAGCTGG | 1130 |
rs572363513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235704432 | TGTTATTTTTGACTT[C/T]TTAGTAATAACCATT | 1130 |
rs572378505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854879 | TTAATCTAAATATGC[A/T]ACCACTAAAAATGTT | 1130 |
rs572378880 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235847183 | CAGCAGATTTCTCAG[A/C]AGAAACCCTATAAGC | 1130 |
rs572397737 | snp | A/G | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828989 | GGGGGTAGACTGCTT[A/G]AGGTCAGGAGTTTAA | 1130 |
rs572414672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235848067 | CATTTCATCCAACAA[C/G]TGCAGAATATACATT | 1130 |
rs572452614 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838978 | CCTACTGCCCTATCC[C/T]CCACCCCTGCGCCCT | 1130 |
rs572464536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824078 | CAGCAGTACTATACA[C/T]TGAAGTGATAATACT | 1130 |
rs572469542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729082 | GATTCTTTAAGGGAA[C/T]AGAGATCAAGTGGTA | 1130 |
rs572487726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235832045 | GAGTACTGCAGTATC[A/G]TTTCTGGGATTTTCC | 1130 |
rs572496384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691760 | GGAGCGCAATGGCAC[A/G]ATCTCAGCTCACTGC | 1130 |
rs572496639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235718850 | CCTCTAATGGGACCA[A/G]TGAATTTTGTTTCAC | 1130 |
rs572512921 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837937 | TCTCTAACAGAGAAA[A/G]GAAAATAGATGAAAA | 1130 |
rs572521115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235683628 | GCATTTCCTAAGATC[C/T]CCTTGAAAGTATTTT | 1130 |
rs572576649 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835948 | TTTCTAATACAACAA[G/T]TGTTATAATGTCATA | 1130 |
rs572592445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825601 | CATCAAAAAGGAATA[A/T]AATATTTAGAATAAA | 1130 |
rs572595542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235824621 | AACCATTAAAAAGAA[C/T]GTTTTTGATATTTAA | 1130 |
rs572597207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235816515 | ATTTACAGATTCAAT[A/G]CTATTCCAAACTACC | 1130 |
rs572598890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685702 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGTG | 1130 |
rs572608324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804360 | ATCACATATCCATCA[C/G]GAGGAGATAAGATCC | 1130 |
rs572633739 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LYST | GRCh38.p7 | 1:235817578 | AGCAATATGGATGGA[A/C]GCTGAGGTCATTATC | 1130 |
rs572634044 | in-del | -/CATGTTCCTGATTTGCTTC | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235815098 | AGTAAACTTAGCTTT[-/CATGTTCCTGATTTGCTTC]CATTCCAGCAAACAC | 1130 |
rs572634281 | snp | A/G | 1.8177e-05 | 0.00301466 | intron-variant | LYST | GRCh38.p7 | 1:235752208 | GAAAACAGAACATTT[A/G]TAAGAAAAAGAACAA | 1130 |
rs572686810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235690724 | CTAAAGAGCTCAGGG[A/G]ATGGGATACATTTTA | 1130 |
rs572690382 | in-del | -/T | 0.369346 | 0.219673 | intron-variant | LYST | GRCh38.p7 | 1:235757884 | ATGCTATTGGAAATG[-/T]TTTTTTTTTTTTTTT | 1130 |
rs572719078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235751596 | GCTCATAAATTTATT[C/T]CATTTTAAAAATTGT | 1130 |
rs572721826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235795039 | TTAAAAATATTTCTT[A/G]AAGATGGAAAAGTAG | 1130 |
rs572731291 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235873218 | AGATGACCTTTCCAA[C/T]CAACTAAAAGTGTTA | 1130 |
rs572785387 | snp | C/T | 7.58093e-05 | 0.00615621 | intron-variant | LYST | GRCh38.p7 | 1:235830168 | TAATCCAAAACCATG[C/T]AGCTACAGTTAACTA | 1130 |
rs572806542 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235802316 | ATCTTTTCCATTCTA[A/C]TCATTTTAAGTCCAA | 1130 |
rs572810936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235862167 | CAGTTGATATGATAT[C/G]ATATGACTGACATAA | 1130 |
rs572824975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235727021 | TATAAATGAGAAAAG[A/G]ATGCTGTTCATATTT | 1130 |
rs572830190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682801 | TCTATTTTATTTTTT[C/T]CCACACATGCTTTGT | 1130 |
rs572831465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669639 | TGGGATACCACTTCA[C/T]TCACATGACGTGAGC | 1130 |
rs572846725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235780001 | CTAGCTCCTACATTA[C/T]ATACTGGTAGAACAA | 1130 |
rs572847343 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235870071 | GGGCCTCTGCCCTGG[A/C]CCCCACACATGAATG | 1130 |
rs572889392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877697 | AAGCGTGAGCCACCG[C/T]GCCTGGCCGGTCAAC | 1130 |
rs572897845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235801770 | AAAAAATTAATAAAC[C/T]AATATTTTTTCAAAA | 1130 |
rs572914019 | snp | C/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740118 | GAAAAGGAAGACAGT[C/G]CCCTCAGTGTACTTG | 1130 |
rs572934337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786717 | TGGAATACTATGCAG[C/T]CATAAAAAAGGATGA | 1130 |
rs572959468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802369 | AGGCAATATAGTTCC[A/G]TCCTAAAGACAAATT | 1130 |
rs572959896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235820098 | ACCAACAAGGTGCCA[A/G]GCACTGGCCCTTTTC | 1130 |
rs572970375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766451 | TTATTTCCTAATTCA[A/C]GCAATCTTGTTATTA | 1130 |
rs573000304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235837316 | AACAGAAAAGAGTAA[C/T]CAATGCTATCAAAAA | 1130 |
rs573006736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235774238 | AAAACAAACAGCACT[A/C]AATTTTTATGTTTTA | 1130 |
rs573006829 | snp | C/T | 3.31274e-05 | 0.00406972 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766096 | ATGTGCAAAGAAAAG[C/T]AGAAGTTCGTGGGAT | 1130 |
rs573015794 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235811240 | ACATAAGAGATGCTG[C/T]AGATTATCTGGTATT | 1130 |
rs573059442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235734797 | TACAAAAGACATTCT[A/G]AGGATAAGTACAGAA | 1130 |
rs573070857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771268 | ACAAACAAATACCAA[C/G]AAAAAAAGAAAAACG | 1130 |
rs573074791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235778467 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 1130 |
rs573080156 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883661 | TTTTCGTTTGGTAAC[A/G]GGGCTAGGAAATCTC | 1130 |
rs573096560 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235731392 | AGTCTCCCAGTTCCT[C/T]GCCTGAAGGCAAGCT | 1130 |
rs573098383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235779640 | GGAACCATTTCCCTA[A/C]AGGATGTTTTCTTAA | 1130 |
rs573100227 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806374 | GTATCTTCTGAGTCA[C/T]TGGCCGACTCCCTGT | 1130 |
rs573113094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235777889 | GTCAAGATTCTCTAA[A/G]CTATTTTAAAAATTA | 1130 |
rs573113593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235830514 | GTTGTTTGTTTCTAA[C/G]TGAAGATTGGCTTAA | 1130 |
rs573116970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875143 | TGGTGGGAAAGATCA[C/T]GGTGGTTTGAAGATC | 1130 |
rs573118003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235742141 | ATTATTTATTGGGCA[C/T]GGAGTTTCATTTGGG | 1130 |
rs573122785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807592 | AGTTGTGCTAAGATT[G/T]ACCAAAAAATGCCAC | 1130 |
rs573131647 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235690882 | GCAGCAGCATACTGT[A/C]TATTTACATGGTATT | 1130 |
rs573158274 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235815743 | GGAAGGTGAAAGATT[C/T]CTACAATGAGAATTA | 1130 |
rs573176312 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235759986 | ATATCTTCCCAAAAC[-/AT]ATGTTTTTTCCTGTC | 1130 |
rs573179125 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868765 | CAGTGGCACAGTCTC[A/G]GCTCACTGCAACCTC | 1130 |
rs573194151 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235688563 | TACCAAGAAAGCTGA[C/T]AGAGGAAGATGTTTC | 1130 |
rs573206242 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235727978 | GAGTGACAAAGAATG[-/AA]CTCTAATAGTTCTTC | 1130 |
rs573217124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695442 | CAAATTCCAAATACA[C/T]TGTGCGAAGAAATTA | 1130 |
rs573218125 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884441 | GCTAATTTTTTAATG[A/C]CCAGGCTGGTCTTGA | 1130 |
rs573233156 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235772048 | GGCAATATAGTGAGA[C/T]TTCATCTCTACAAAA | 1130 |
rs573241612 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235797568 | AATTGGATATTCACA[C/T]GCAAAATAATAATAA | 1130 |
rs573243405 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235666730 | GTATGCTAAAGAAAT[A/G]GAATTATAGACAATA | 1130 |
rs573250527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235701853 | ATAAGTTTTGTTTGT[A/T]TTTAACATGAACATT | 1130 |
rs573255856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235663847 | GGGTCACGGACAACC[C/T]GCTGTGTGTTAAGTG | 1130 |
rs573257816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739603 | CACAATAAACCTTGA[A/G]CAGTGAAAAAAAAAA | 1130 |
rs573305803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235757950 | CATGTCAGAAAAACC[C/T]AGTTCACTCACAGAG | 1130 |
rs573310180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235708754 | GATTCTTGGATGTTT[G/T]TGCCTGCTTTCTCCC | 1130 |
rs573312157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851873 | GAATAAGAAAATTCA[C/T]GAAAACCAATTTAAC | 1130 |
rs573334040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235793293 | ATAATCTCAGCGATA[C/T]GTCTGGTTAATCCAA | 1130 |
rs573344084 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235825020 | TTGAGACTCTGTCTC[-/A]AAAAAAAAGAAAACA | 1130 |
rs573388118 | snp | C/T | 0.000378573 | 0.0137529 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853083 | GCCAACTCCCAGGCA[C/T]GCCTCCAAGCACCAC | 1130 |
rs573395064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235749151 | AAATGGACTTGAATT[A/C]GTTTTTGTAACCACA | 1130 |
rs573397401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785770 | CTACATTACAGTTTC[A/G]AATTCTCTATCTTCT | 1130 |
rs573399956 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778201 | TCCTCCTGCCTGTGC[C/T]TCCCAGAGTGCTGGG | 1130 |
rs573410316 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867951 | ATTATGTCCCAAGCC[A/T]ATATACCAAATGTTA | 1130 |
rs573428013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235822065 | GAAACTCACAACATT[C/T]TAAAGAAAGTTGGTT | 1130 |
rs573429796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235829529 | AGAGTTTTACGATCA[C/T]AAAATAATTATTCAT | 1130 |
rs573441373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235882237 | GAAAGATATTCCAGG[C/T]TGAGGGAATAGCATA | 1130 |
rs573453118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235764059 | CCTTGTTTCATAAAT[C/T]ACATTTCAGCAACAC | 1130 |
rs573476176 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235864680 | CTCACGCCTACAATC[A/G]CAGAATGTTGACACG | 1130 |
rs573484938 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235749220 | TTGTACCTGTAGCAT[A/G]CAAAGCCAATATACT | 1130 |
rs573489514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815000 | CTCCATCCCCATCCT[A/C]CCATCTGCCAAACTG | 1130 |
rs573522212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235674641 | CCATTAAAGGAATAG[C/G]TGAACAATTAGGTCC | 1130 |
rs573537166 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235843271 | TAAGTAAATATTTTA[A/C]TAGATATTTATTAAT | 1130 |
rs573541897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793439 | TAATTAAAAATACAT[C/T]CTATTAAAAATTGTA | 1130 |
rs573548349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235716570 | GATATTTCATTTCAC[A/G]TAATGATTTCTAGTT | 1130 |
rs573563044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858497 | AACTCCAGAATCTTA[A/C]ATTGAGAATTCTCAC | 1130 |
rs573579777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235747356 | AAATTATGAAAACAT[A/G]TATCAATTTCTATAA | 1130 |
rs573588703 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235710177 | AAAACAGTTAGAAGG[A/T]TCTTCACCAAAATAC | 1130 |
rs573599520 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235850858 | AAGAATGGCCATAAT[A/C]AAAAAATCAAAAAAC | 1130 |
rs573602393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792846 | TTTTTGTATTTTTAG[C/T]AGAGACGGGGTTTCA | 1130 |
rs573646713 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676923 | TGAGGCCTAAATTGA[C/T]GCACTCAGTCTTGGA | 1130 |
rs573653241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827353 | CAGCCTGGGTGAAAA[A/C]GTGAGACTCTGTCTC | 1130 |
rs573670467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688268 | TCCTGAAACATTTAG[C/T]GATTTCATCATTCTA | 1130 |
rs573712134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762621 | GTTAGATTGAATGAG[A/G]TTGTACTACATATAC | 1130 |
rs573720301 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235813266 | TGATAGAAGAATCTA[A/C]GAGTATTTGACAGTA | 1130 |
rs573754595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235707179 | CAGGCCCATCTACCT[C/T]GGAGAGGAAAGTTGG | 1130 |
rs573771169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235714358 | AGAGAAAGGGAACAG[A/G]CCAACAATTTTCAAA | 1130 |
rs573773756 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713608 | TCTCACAACTGGGGG[G/T]ATGGGGTGTGGGTGG | 1130 |
rs573789550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828029 | GAAAAAATGCTCAAC[A/G]TCATTAGTTGTTAGA | 1130 |
rs573803944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235722537 | GTTGCCCAGGCTGGA[C/G]TGTAATGGCGTGATC | 1130 |
rs573813851 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235699828 | ATTTCTCTAATGATC[A/C]GTGATCCTGAGCTTT | 1130 |
rs573828619 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847452 | ATCACACAGGGCCTA[C/T]AGAACAAAAATGCAA | 1130 |
rs573832581 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235877566 | CATGCACCACCACAT[C/T]CGGCTAATTTTGTAT | 1130 |
rs573847173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665889 | GGGCTGATGATGATA[C/T]GTCCAGCCTTCTCTG | 1130 |
rs573872430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235755320 | CTTGAACCTGGGAGG[C/T]GGAAGTTGCAGTGAG | 1130 |
rs573872678 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235756071 | TATATCTGTATCTAT[A/C]TCTATCCTAGACCTC | 1130 |
rs573889333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843375 | ATGACAGTAGTGAAA[C/T]AGGACCCAGAAGCCG | 1130 |
rs573918981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235798314 | TCAGTTAATAATAAC[A/T]TATCAATATAAGTTC | 1130 |
rs573943741 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LYST | GRCh38.p7 | 1:235785790 | CTCTATCTTCTTTCA[C/T]GCTACTTCATTCAAT | 1130 |
rs573994978 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235679382 | AGCCCCTTCCTTTTC[C/T]GCTTGGGTTCTGCAG | 1130 |
rs573999150 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235837550 | GAGAACTGCTTGAAC[A/C]TGAAAGGGGGAGGTT | 1130 |
rs574007894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834007 | GCGGAATATCTAAAT[A/C]CTATCACGACAAAAA | 1130 |
rs574014665 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235856676 | ATATTTCAGTAATGT[A/G]GAGCAAATGACTTTA | 1130 |
rs574040792 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235693265 | AGCTTGCAGTGAGCC[A/G]AGATGTGTCACTGCG | 1130 |
rs574058552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673090 | AAACAGTAATCCAAA[C/T]TGCTGAAAAAGGGTA | 1130 |
rs574065136 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765060 | TTTCTTCAGTGGTCT[C/T]ATCTGTTCTCAGAGC | 1130 |
rs574074962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235761998 | GGAGGGGGGAGGGAT[A/G]GCATTAGGAGATATG | 1130 |
rs574080334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235820526 | AGGCACGTGCCACCA[A/C]ACCTGGTTGATTTTT | 1130 |
rs574092172 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804518 | CCTTCTCAGTCATAG[C/T]ATCATTATGTTCAAA | 1130 |
rs574092452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672530 | TATACCTAGAAAAAA[A/G]CAACTTTGGCTGCTT | 1130 |
rs574097561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235881133 | TAAGCAGGTCATAAC[A/G]AAGTGGTAACTACAA | 1130 |
rs574100182 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235774525 | GAAAAACTAACTCTG[C/T]AGCAGCAGTGCCTAA | 1130 |
rs574126280 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687400 | GTGAATGTATGTGTA[C/T]TTCACATATTTATTT | 1130 |
rs574161700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235790527 | AAAATTCAATCCACA[A/G]CAGAAAATTCTAGTG | 1130 |
rs574162253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235771460 | CCAACTTTGTCCAAG[C/T]TAGGTTTTCCAACCT | 1130 |
rs574173435 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235698593 | AAAGTTGAGAAAGGC[C/T]GGGCGCGGTGGCTCA | 1130 |
rs574193563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235849216 | GGATGGTTTAACATA[C/T]GTAAGTCAATAAATG | 1130 |
rs574219933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235776793 | TTTAAAAATATCCTC[C/T]TCTCAATTTAAAATC | 1130 |
rs574242508 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235745510 | CTCTGGAAAAGTTTG[G/T]CAGTTTCTTAAAAAA | 1130 |
rs574251996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235811671 | AAAAAGTAGCTGTAA[C/T]TTAGAGTGAATAAAT | 1130 |
rs574257693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235782871 | CTAGCCATTGAAATG[C/T]CAATACTTTCTGCAT | 1130 |
rs574259691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729987 | CTGATACTTCAGATA[A/C]ATTTTTTGTGTGTGC | 1130 |
rs574294596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738179 | AGACAAATTGAAGGG[C/T]GAGATGATGGATCTC | 1130 |
rs574302076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791276 | AACAAGAGTGAAACT[A/G]TCTCAAAAAAAAAGA | 1130 |
rs574311884 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704464 | TGACTGGTGGGAGAC[A/G]GCATCTCACTGTGGT | 1130 |
rs574314495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235819600 | CTATTTCTAGACCAC[C/G]CAATCAAGAGAAATC | 1130 |
rs574318289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235768164 | TGCTGTAATTTCAAA[C/T]GTAGATACAAAAACT | 1130 |
rs574321213 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821210 | TGGGAGGCCAAGGGG[G/T]GTGGTTGCTTGAGCT | 1130 |
rs574324910 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235782736 | TAATTTTGCCAAGAA[A/G]TCTCCCATCTTGACA | 1130 |
rs574343386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235760344 | CAAAAAATGGTAGTA[C/T]TTGTTGTTACTAGCC | 1130 |
rs574370562 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235743252 | AACTGGAAGCAGTAC[A/C]TTCAGAATTCATTCT | 1130 |
rs574373590 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235855169 | TACTGTATTGTTTCT[C/T]TTAAAACTAGATTAT | 1130 |
rs574379256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235767615 | ACTGACTCTTTATCA[A/G]TAGTCACTGGTATTC | 1130 |
rs574389174 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866017 | TCTGCCGAGCGGATC[-/G]GGGATGTTTTGCTAT | 1130 |
rs574406087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235746120 | TGGAAGTGCCATATG[A/G]TTTTAAACTGGTCAG | 1130 |
rs574432101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235698056 | AAGACATGATGCCCT[C/T]TTAAAGAGTTTCCCC | 1130 |
rs574434993 | snp | A/C | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739123 | GGAAAAACATCAATT[A/C]CTAAGGTTAGAAATA | 1130 |
rs574445673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235751513 | AGACATTTTTAAATT[C/T]TTGTTAAAAGCAATT | 1130 |
rs574472713 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235818524 | CCCCATTTCCATGTG[A/C]TTTACTTCCAAATAA | 1130 |
rs574475323 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708376 | ATGTAGGATAGTGTG[C/T]GGAAAAGAGTTAACA | 1130 |
rs574479723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235761104 | TTTATTTAAAAAAAA[A/T]TTTTTTTAAAAAGAA | 1130 |
rs574484936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863935 | GAACCCTGCTAAGTC[A/T]GTTTAGCATAACATC | 1130 |
rs574518905 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235748856 | GAGTAAATTTGTCTA[G/T]TATCAGAGTCTGGTG | 1130 |
rs574521745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235864653 | AGGCAAGCCTGGGGC[C/T]GAGCGCAGTGGCTCA | 1130 |
rs574523041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235877776 | GCATCGCTTAGCAGT[A/G]TAGATGTAGCCCAGG | 1130 |
rs574548467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235856167 | TCACTGTGGTCTAAA[C/T]GTAGACTTGTATAAA | 1130 |
rs574559915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235789198 | ACCCTGGTCCAGGGA[A/G]CACACATCATTGTCC | 1130 |
rs574577203 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235753363 | TCATCTTGCTAACTT[G/T]ATTTTGAAGTCATAA | 1130 |
rs574606768 | in-del | -/A | 0.0651284 | 0.168293 | intron-variant | LYST | GRCh38.p7 | 1:235663084 | AATGTAAGGCTGTAA[-/A]AAAAAAAAAAATTCC | 1130 |
rs574615927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752510 | TAGGCAGTTTCTAGT[C/T]CACACTAAGGATGAA | 1130 |
rs574620429 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235728202 | ATGGTTTAATGCATG[G/T]TCTCTGGAGTCCTTT | 1130 |
rs574627212 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701875 | ATGAACATTTGACAT[A/T]TGTGAGCTATGAGCG | 1130 |
rs574631915 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885445 | ATTGATGCTAATCAT[A/G]TGATCTTCTGGATCA | 1130 |
rs574640488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235824759 | GAGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 1130 |
rs574640618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235831841 | AATCCAATAACCTAA[A/T]TTATATTCAGTTCAT | 1130 |
rs574700162 | snp | A/G | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660822 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 1130 |
rs574719540 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235861808 | CGGAGACTGATAGAC[A/T]TTTTATCCAAGTTTT | 1130 |
rs574758202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853344 | ATATTTAAAATGTGG[A/G]AATATAATAATCCTT | 1130 |
rs574759874 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720723 | AGCAAGTATAAATGG[C/G]AACACAGGATACTGC | 1130 |
rs574760980 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693975 | TATGGTAGACCTTCA[C/T]TCAATTCAAGGAGGC | 1130 |
rs574763360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796398 | GCATCTAGAATACAT[A/G]AAAAAAACCTCTTAC | 1130 |
rs574772498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825441 | TTACATACAAAATCC[C/T]AGGGAATCTACAGAA | 1130 |
rs574815539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846949 | AAAAGCTTGGAAAAC[A/G]TATCTGGGTGGATAA | 1130 |
rs574843783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235797903 | ATATCCAGAATATAT[A/G]GAGAACTCTTAAACC | 1130 |
rs574845699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235830064 | GAAAGTATTCAAATA[A/C]ACAATATGGTTATAA | 1130 |
rs574852329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235839132 | ACCTGGCCTCATTTT[C/T]GTTCTCTACATATAA | 1130 |
rs574869092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691170 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGCGCT | 1130 |
rs574869244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235697435 | CTTCCCCATGCTTAG[C/T]GTATAGAAATATTTG | 1130 |
rs574900657 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235689399 | TCTGCCAGGCACAGA[A/C]AGACAAATACTGTAT | 1130 |
rs574905913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235696918 | CTGCATTTAACTCTC[C/T]GTTTTTTCATGTAGC | 1130 |
rs574910384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803637 | ATAAAAATTCCACTA[A/T]TACCTTCATTTTAGA | 1130 |
rs574924228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235788644 | TCACATTAATGTCTC[C/T]TACACAAATTATTTA | 1130 |
rs574939752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235816348 | CGGGAGCTGAGGCAG[A/G]AGAATCACTTGAACC | 1130 |
rs574945763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235765911 | TTTAGACTCCTTGAG[C/G]ACAGAGGCCATGTCT | 1130 |
rs574965493 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235730546 | ATGTACCCATATATG[G/T]GTATATATATACATA | 1130 |
rs574965930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709962 | ATATCTAATTGTCTC[A/G]TCAGTATAAACAAAA | 1130 |
rs574966879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235726940 | CCTTGGCTGATAAAA[G/T]GATCCATCTTGAAAA | 1130 |
rs574967110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235717696 | GTCTGCTTAACCACA[G/T]GTTGATACATCTTTT | 1130 |
rs574972483 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | LYST | GRCh38.p7 | 1:235710486 | TCCCAACTTTCAGGT[G/T]TTCTGAGGGAACATC | 1130 |
rs574983912 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235830471 | TAGGAAAACAAATAC[A/G]AATTTACTTTTAAAA | 1130 |
rs575010888 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859077 | CCTTCTCAATCTCAG[C/T]AGATAATCTTGCTTC | 1130 |
rs575024479 | snp | A/G | 8.24042e-05 | 0.00641836 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759264 | CTTTGACCACTGGAA[A/G]TCCCAGCACTCCCTT | 1130 |
rs575030364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691701 | CATCAGATTCTCTCT[C/T]TTTTTTTTTTTTGAG | 1130 |
rs575032804 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235846237 | CGGCCTGGAGCCAGG[G/T]AGACTCGCTGGGTGG | 1130 |
rs575035511 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LYST | GRCh38.p7 | 1:235702562 | AGCTCCCCAAAGCAC[A/T]CTCTCATATCGCTAA | 1130 |
rs575049580 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838827 | GTACCCTTCTTAGTC[C/T]GTGTGTAGATCATTC | 1130 |
rs575075394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235695372 | GAACTGCCTGTGGAG[C/G]CCATGGAGGAAACTG | 1130 |
rs575083642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235802264 | AGCATATAAAAAGAT[A/G]GAGTCTTGCCAGAAG | 1130 |
rs575084575 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661117 | TGATAATTTACAGAA[A/G]TGTTTGCTACAACAT | 1130 |
rs575087260 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809157 | CGCAAGCACTGATGG[A/G]CACACACTGCAATGC | 1130 |
rs575105861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758813 | CTTAAAATAAGGAAA[A/C]ATATATCTTTCTGTT | 1130 |
rs575118764 | snp | A/C | 9.80777e-05 | 0.00700209 | intron-variant | LYST | GRCh38.p7 | 1:235806806 | ATGTAAAAAGGTTTA[A/C]ATAAAGAAACATCAT | 1130 |
rs575147865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235803181 | TGAAGAAAAAAACTT[A/C]GTAAACAATATGAAT | 1130 |
rs575203232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235666645 | ACACACATGCCCAAT[G/T]TTCTACTAAGTTTTC | 1130 |
rs575210211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235786659 | CAACCCAAATGTCCA[C/T]CAATGATAGACTGGA | 1130 |
rs575211637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235868986 | AGGCATGAGACACCG[C/T]TCCTGGCCTCGGTTC | 1130 |
rs575211752 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | LYST | GRCh38.p7 | 1:235725433 | GTGAGACTCTGTCTT[-/A]AAAAAAATAAAAAAT | 1130 |
rs575239134 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792619 | CATGCCCAGCCTTCA[C/T]TCTTAAAATATGTAA | 1130 |
rs575244972 | snp | A/C | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868771 | CACAGTCTCGGCTCA[A/C]TGCAACCTCCGCCTC | 1130 |
rs575246194 | snp | C/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809709 | GCAAAAGGGTCAGGC[C/T]GCTTTTCTAGGCATA | 1130 |
rs575258707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235877046 | GCTCCTTACCTGTTT[G/T]CTAGATATTTCTATG | 1130 |
rs575289371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235779334 | TATGACCTATATACC[A/G]TTCAGGAAAAATAAA | 1130 |
rs575300942 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235787777 | GGATTACTGAAAGAA[C/T]GAGGAGATAATGTAC | 1130 |
rs575334802 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235794336 | GTGGAAATATTAAAG[A/T]TGATTTAAATACTTA | 1130 |
rs575335981 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884402 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 1130 |
rs575371917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235807547 | AATGACTGTAAGGCA[C/T]TGATTTAACATCAAT | 1130 |
rs575391286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235845005 | GGCAGGACTAGATTG[C/T]AGCTCTGGACAGAGC | 1130 |
rs575407160 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYST | GRCh38.p7 | 1:235737578 | AAGGTGGGCCTGGGA[C/T]ATTCTTCTGTGCCAG | 1130 |
rs575410854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785035 | GACTGTAAAGCAATC[C/T]ACAAGCTCCTGCTCC | 1130 |
rs575417594 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235801642 | CAGTTAAGAAATTTA[C/T]AAATTTCTACCTAGA | 1130 |
rs575420430 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235714324 | AAGGATAATTAGCCA[-/G]GGGAAAAACAAGAGA | 1130 |
rs575436548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235852322 | CCCCCAGCCCCCTGC[C/T]TGTCAGGGAGGGAGA | 1130 |
rs575445379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235784399 | CTTACTAATTTCAGA[A/C]TGTCCACAATAAAAA | 1130 |
rs575463484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235749104 | ACATGACAGAAATAG[A/G]AATCCCTCTATGTCC | 1130 |
rs575466061 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235710465 | CATTTGTACAAACTC[A/C]ATCTTTCCCAACTTT | 1130 |
rs575475581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235845470 | CTAACAATTTGAACG[C/T]GGTGAGAAGCCTGCT | 1130 |
rs575514714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235673921 | ACACCTTAAATAAAA[A/G]CGATTGTTGCGCTTT | 1130 |
rs575516599 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235763865 | ATTTCTAAATGGTAT[A/C]CTTGATGAGCATCTC | 1130 |
rs575517273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235763381 | TTTGGGAAGTTCCCA[C/T]GTGGTAACCTGGAGC | 1130 |
rs575525901 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235798492 | AAAACTGAAGGAGAA[C/T]TGCTTAACCTGGGAG | 1130 |
rs575545548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707875 | TTCAGGGTTTTTTTG[C/G]GGGGGGATTTTGGAA | 1130 |
rs575555630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771194 | GACAAGGCAGCCAAA[C/G]TATGAAAACATGATT | 1130 |
rs575558486 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235771976 | CGCCTGTATCCCAGC[A/C]CTTTGGGAGGCCAAG | 1130 |
rs575570513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235777851 | CCAGGCAAAGGATAG[A/T]TTCCATCAGTGTGTG | 1130 |
rs575574389 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756509 | GCTCAGGGACTTACA[C/T]ATGAAATGCGAGCTC | 1130 |
rs575585205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235716402 | AACACTAGGGGATAC[A/G]AATAGCAGGTCCCTG | 1130 |
rs575585896 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235832027 | CATGCCACAGCACTT[-/A]AAGAGTACTGCAGTA | 1130 |
rs575591135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874942 | TTCCAAGCCCAGGCT[C/G]CTCCTCCAACCAGCA | 1130 |
rs575624567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235749573 | GGGTCTTAAGATGAG[A/G]AAGCTGGACTGGATG | 1130 |
rs575646910 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235768984 | TTTATCAGATGCCCA[-/G]GTGTGTCAAGTACTG | 1130 |
rs575648379 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235708726 | GTATGCTTTTTGTGC[C/T]TTACCAGGGGTAGAT | 1130 |
rs575653853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235851832 | CAGGGAAAGATATGA[C/T]ACTTAAAGTTCTAAA | 1130 |
rs575654471 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673711 | GCTTCTTTGAAATGC[A/G]CTTTGTTTCTTCCCC | 1130 |
rs575706498 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867195 | GGTCGGGGGTCGTAC[C/T]CTGGGTCCGCACCTC | 1130 |
rs575708756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235680811 | CCCATGTTGGCCAGG[C/T]TGGTCTCGAACTCCT | 1130 |
rs575709136 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235688058 | TTCAGTTTCTTTCTT[A/G]AGTAGTTCTATTTGT | 1130 |
rs575723800 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235826001 | ATCAGTGGAACACAA[C/T]GCAGTCTAGAAAGAC | 1130 |
rs575736591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235858585 | TGACTCATTTAGATT[A/C]TTCATCCTCTTCATT | 1130 |
rs575742574 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867756 | CCTAGTCACTGAGAC[A/G]GCAACGCCAGAGGTA | 1130 |
rs575764162 | in-del | -/AAGATTCTGCAAAATAAGTTTTAG | 0.0448719 | 0.142907 | intron-variant | LYST | GRCh38.p7 | 1:235855704 | TTTTGCATAAGGTTA[-/AAGATTCTGCAAAATAAGTTTTAG]AAGATTCTGCAAAAT | 1130 |
rs575770149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235688104 | ATAAATTTTATTCTT[C/T]CTTGGAGGTCTTCCA | 1130 |
rs575772378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235882044 | TGTATATTTAAACAC[A/G]CACACTCACACATAC | 1130 |
rs575781507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235881435 | GAGGAAAAATAATAG[A/G]GGTGTGAATTACCAT | 1130 |
rs575808124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235874208 | AAAATGTCTCCAACT[C/G]TACCTAGTCCCACAC | 1130 |
rs575808799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793322 | AAATTGAAGTGAAAT[G/T]GTTAAAATATATGCA | 1130 |
rs575816514 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685285 | GTTCTGGCTCCTTAA[A/C]CTGCCCTTCTTTGCT | 1130 |
rs575829422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872496 | ATGCCTGTCTGTTCC[A/G]ATTCTTCTTGGCATC | 1130 |
rs575845188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740280 | TTGAGGTATAACTTA[C/G]ATATAATAAAGCATA | 1130 |
rs575921123 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235754234 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 1130 |
rs575921191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762446 | AGACAGAAGAGAATA[A/G]AAGTTTTTAAAAAGC | 1130 |
rs575937768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235799616 | TTAATTCTCCAACTA[A/G]AATTTAGATTTCTTG | 1130 |
rs575938459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235681438 | CCCCGAAGCAATAAA[A/G]GGTCACTGAAGTGTC | 1130 |
rs575952592 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675875 | GAGAACTGGTTAGTC[C/T]CTGGAAAAACACCAT | 1130 |
rs575952855 | snp | A/G | 4.94613e-05 | 0.00497275 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746389 | CTCTGTAGTCTCTGC[A/G]CAAGTTCCGTTTCAG | 1130 |
rs575959260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732037 | ATTCATACCCTAAAC[A/G]TACCAAAATACTGGT | 1130 |
rs575998944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235850139 | TATACTATAAGGCCA[C/T]AGTCACCAAAATAGT | 1130 |
rs576007372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792426 | TTCAGGCGATTCTCC[C/T]GCCTCAGCCTCTGGA | 1130 |
rs576019456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732716 | TAGCAATATTGAATA[C/T]TTTCCCGTGTGTTTG | 1130 |
rs576043087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739477 | ATAATTGTTCCAAAG[G/T]ATCTTATTTTGTGAA | 1130 |
rs576069862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747285 | ATAGGAACCAAAATG[A/G]TGTCTTGGTAGATGA | 1130 |
rs576080925 | snp | A/G | 3.29821e-05 | 0.00406078 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806298 | CAAGACAAGGCTCTC[A/G]AGAGATATACATGGC | 1130 |
rs576085237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699764 | TGACTTTTTAATAAT[C/T]GCCATTCTGATTGGT | 1130 |
rs576085672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235872004 | TTAATCAGAGTTTTA[C/T]GTAACATGGGGCCAA | 1130 |
rs576104852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235843970 | AAGTTGCCATTGGAA[A/G]GACTTTTTTTCAAAA | 1130 |
rs576120361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235769266 | GCAAAAAGAATACCA[A/T]GTACTCTGAGACAGA | 1130 |
rs576125764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235699191 | GTGGTTTGCTGCACC[C/T]ATCAACCCATCATCT | 1130 |
rs576130829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235729819 | AAAATATTAGCTCCT[C/T]TTTAGCATTCTATTA | 1130 |
rs576150855 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235823127 | ACTGATATATTCATT[-/G]CTTCAATCAGTCTGG | 1130 |
rs576178210 | in-del | -/AAG | | | intron-variant | LYST | GRCh38.p7 | 1:235856042 | GCACAGAACAGAAAT[-/AAG]AAAGAAATATATATA | 1130 |
rs576185139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235842982 | CAAGTCATGACCACA[C/T]ATATTCTTCACTTTT | 1130 |
rs576186405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235768464 | AGTGCACAAACACTC[C/T]GAGGTAACTTAAAGG | 1130 |
rs576215146 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235713504 | AATTCCCATTATCTA[C/G]AATATGCATATATTA | 1130 |
rs576220533 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869299 | AACACGGTGAAACCC[C/G]GTCTCTACTAAAAAT | 1130 |
rs576221063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235834976 | CTTGAGTGCAGTGGC[A/G]CGATCTCGGGTCACT | 1130 |
rs576247259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235694070 | GCTGAAGTGCCGTGG[C/T]GCAATCTCGGCTCAC | 1130 |
rs576262891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235857875 | CACTTTGGGGGCCAG[A/G]AAGACAAGTCAGTAT | 1130 |
rs576268070 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673643 | GCAACTCTAACCCCA[C/T]CTTAGGTGCTTCTAT | 1130 |
rs576278280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235672347 | AGACAAGAGACCTAA[C/G]GTATGCCATCGTTAA | 1130 |
rs576289766 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYST | GRCh38.p7 | 1:235849506 | AACATAGTACTGGAA[A/G]TCCTAGCCAGAGCAA | 1130 |
rs576369931 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680950 | ATGTGGAGGGCAACC[C/T]ATACATTTATTCATC | 1130 |
rs576389001 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235817881 | AAGTAAAAAAAAAAA[A/T]TTGTTACCACAAAAA | 1130 |
rs576405814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235685770 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAGATTG | 1130 |
rs576413659 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673727 | CTTTGTTTCTTCCCC[A/G]CTATCCTCTATTGTT | 1130 |
rs576415331 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYST | GRCh38.p7 | 1:235880464 | TCATTTGACACCGTC[A/G]TAACAGTGACTAAAC | 1130 |
rs576420106 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235880303 | GGCTTGCCTTATACT[A/G]CCTTCCCTTGTGGAG | 1130 |
rs576433015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235767592 | GTTACTTCTATCTTG[C/T]CCTCTCCACTGACTC | 1130 |
rs576433116 | snp | A/G | 3.30278e-05 | 0.0040636 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809612 | TCCTTCCAAAAGCTC[A/G]GGTAAAAGAAGGGCT | 1130 |
rs576440416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235813160 | AAAATCCTTTTTCTT[G/T]AAAGTCTGCATTTGA | 1130 |
rs576466734 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826574 | TGGTCTTGCAGTGAG[C/T]GAAGGGGAGGGACTG | 1130 |
rs576486207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235782639 | GGAAATGTGACTAAA[C/T]ATTTGCTGCAAGTTT | 1130 |
rs576491982 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235806931 | GTTCTTAGTTAGATA[A/T]AATTAGGACCTCAAG | 1130 |
rs576518026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235775600 | CTAAAGGCCAAAGAA[C/G]AATGAGACAATAGGT | 1130 |
rs576522471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235790442 | GTGACACATACACAG[A/C]AAGCACTCAATGCAC | 1130 |
rs576528873 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235818693 | GGTAGAGTCCTCCTA[A/C]TCTGAGTCTTTATCT | 1130 |
rs576528902 | snp | C/G | 1.66197e-05 | 0.00288263 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809989 | CTAAAGGAGAATTAT[C/G]ATTCAAGGTAACGTC | 1130 |
rs576533435 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235831189 | AGATGTTAAGTTAAA[C/T]AAGACATGTATTGCC | 1130 |
rs576540716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235670100 | AATTAGCAAACCTCT[A/G]TATGCCCAGACATGC | 1130 |
rs576570460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804891 | CTTATTTGGTTTTCA[C/T]TGCAGCATGGTAAAG | 1130 |
rs576595906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235679981 | ATCTTCAATGCTTTT[A/G]AGGCTCTCTCTCTCT | 1130 |
rs576597868 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235671126 | TATTTTTAGTAGAGA[C/G]AAGGTTTTGTCATGT | 1130 |
rs576603770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235804398 | TCATCTGACCAAGTC[C/T]TAGTCCATATGCTCT | 1130 |
rs576610214 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669289 | CTGGTGAGGCAGGAG[A/G]ATAGGGTCTGGAGGC | 1130 |
rs576613379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235798188 | ACTGTTACAGTCAAG[A/G]GGTACCTAAGAAGAC | 1130 |
rs576630367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235848666 | GAGAGAAAATCCAAA[C/T]GACCTCATTAAGAAA | 1130 |
rs576637267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235745399 | TCTGTCAGAATGGCT[A/G]AAATAAAAAATAGTG | 1130 |
rs576639110 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818375 | AGGGCATGGACTCCA[G/T]GGCTCAGGCCCTAGT | 1130 |
rs576659993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235752436 | AAACAGATTACTATA[A/C]ATAGTAAATGGTTGT | 1130 |
rs576713659 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235692312 | TACTCCAGCCTGGGC[A/G]ATGGAGCGAGACTTC | 1130 |
rs576724747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235825377 | GCAAAATAAAAGGCA[C/T]ACAAATTGGGAAAAA | 1130 |
rs576738034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235766556 | CTCACAAGCGTGGTC[C/T]CAAAAGCCAGACTTC | 1130 |
rs576744431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235669731 | GCCCTTGAGCCGCTG[C/G]TTGGGTCCACTTCCA | 1130 |
rs576750858 | snp | A/T | 1.65252e-05 | 0.00287443 | intron-variant | LYST | GRCh38.p7 | 1:235720610 | AACTTTAATAAAGAA[A/T]TACAACATATGGATG | 1130 |
rs576759032 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235878477 | TACTAGCAACCTGAA[G/T]TAAAAATAATGACGG | 1130 |
rs576761941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235789690 | TACTCCCTGTAGCGA[C/T]GACAATAGTTTTAAA | 1130 |
rs576764788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235711421 | AAATTCCAATGTAAT[C/T]TGCCCAACACCAACT | 1130 |
rs576769578 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYST | GRCh38.p7 | 1:235780792 | TTAGAAATCTAATTC[A/G]TAACTATACATTACA | 1130 |
rs576787876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758549 | CTTCCCTTCTGGAGC[C/T]GTCACTTGTCTCTGA | 1130 |
rs576797539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235719768 | TGGGAACAAACCAAA[C/T]GACGTCATGGGAAGC | 1130 |
rs576815017 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235777523 | CAGTGATCAATTGTA[C/T]AGATCACATCAAGGT | 1130 |
rs576828905 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235700384 | TGGTACAAATTTACA[A/G]GAAAAAAACAAACGA | 1130 |
rs576851321 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235688909 | AGAATCGCTTGAACC[C/T]AGGAGGGGGAGGTTG | 1130 |
rs576926116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235691463 | ACCAGTCCATTTAGG[A/G]AAAATCAGGTATAAA | 1130 |
rs576931260 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235701521 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 1130 |
rs576944422 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884525 | AGACATGAATCACTG[A/C]ACCTGGCCCACAATA | 1130 |
rs576954934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYST | GRCh38.p7 | 1:235682397 | CAACAGGCTGCTGGC[A/G]GACATGGAGAGGAAG | 1130 |
rs576982009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235796199 | TTAAAATAATAAATC[G/T]TTATAATCCTGTATT | 1130 |
rs576982707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235863673 | GGAAAAGAATGACTA[C/G]GTTGGTCCAAAAGAA | 1130 |
rs576985447 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235781278 | AAAGTTAATTGTGAA[C/G]CTTTTAATTAAATCA | 1130 |
rs576987685 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885187 | TTCCCATTTTACTGA[A/T]AAGGAATCTAAGACT | 1130 |
rs577002874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235876026 | TCAGTAGTTTGAGAC[A/C]AGCCTGGCCAACATG | 1130 |
rs577003715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743779 | GCTTAAAAAGCAATG[C/T]TTCATGAGTTGAGTC | 1130 |
rs577011993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235830679 | GTAAGTAACAGCACC[C/T]GGATGGAAAACATTT | 1130 |
rs577016995 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868143 | GAAGATTGCCCACTT[C/T]CTCTGGCAGGTAGTC | 1130 |
rs577039436 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235736374 | GTTTTAAAGAAGGTA[C/T]AGAGTGATCTGGGTC | 1130 |
rs577041920 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868861 | CTACCATGCCCGGCT[A/G]ATTTTGTATTTTTAG | 1130 |
rs577050316 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858534 | GTGCCAATTTTTCCA[C/T]CTCTAGTACTCTTTT | 1130 |
rs577075129 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235665561 | AGGTTGCAGTGAGCC[A/G]AGATAGTGCCACTGC | 1130 |
rs577107482 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235731962 | TATCTTAGATGAAAT[-/A]AGACAGGAAAAACAT | 1130 |
rs577120122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235758120 | TCCTGGTGAAAGGAG[A/G]TTTTTTTCATAAAAG | 1130 |
rs577128960 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660868 | GCACTCCAGCCTGGG[C/T]GACAGAGCTAAACTA | 1130 |
rs577164092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852576 | CATTCTCAACAACCA[C/T]CTTAGAAATGAGCCT | 1130 |
rs577170530 | snp | A/G | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660597 | AAAGTTAGGCCGGGC[A/G]TGGTGGCTCACACCT | 1130 |
rs577171883 | snp | C/G | 1.65007e-05 | 0.00287229 | intron-variant | LYST | GRCh38.p7 | 1:235728041 | TTTGGAATCTGTCTA[C/G]ATTTATGTAAATACA | 1130 |
rs577180316 | snp | A/C | 3.29755e-05 | 0.00406038 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728100 | AACTGTATCAGAAGC[A/C]TTATCTTCCACAAAA | 1130 |
rs577180318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235710455 | TGCATAAGGGCATTT[A/G]TACAAACTCAATCTT | 1130 |
rs577211955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235736802 | GGGACAGAATATTTA[A/C]ATGTGTAAATACATG | 1130 |
rs577244425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235743274 | ATTCATTCTGAGTTT[C/T]AAAAACAGCTCCTCT | 1130 |
rs577254851 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235724714 | CTGGCAACCACTAAT[C/T]TGTTTACTGTCTCTA | 1130 |
rs577275321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235875394 | TTAAATATCCTGGGA[C/T]AAATATCTTGGGGCT | 1130 |
rs577285188 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872827 | AGGCTTAGGCAGGAG[A/G]ATCGCTTGAACCTGG | 1130 |
rs577285772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235702526 | GTTACCGTCTGAAAC[A/G]ATGAATTCTTTTTTC | 1130 |
rs577307551 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235696798 | TATTCTGGGGCTCAA[A/C]AGCCTCAAAGTGTAC | 1130 |
rs577320258 | snp | A/T | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733673 | ATCCTTTGATTTTGA[A/T]TCCAGACGCTGAAAG | 1130 |
rs577325609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235823504 | CATTGCCTATTCCCT[G/T]GCTTTAAAATTTCCC | 1130 |
rs577339619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235667766 | CCGCTTCCTTCAAGC[A/G]ATTCTCCTGCCTCAG | 1130 |
rs577378632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235779227 | CCCAAATTACTAAAT[C/T]GGGCTTAAACAATTT | 1130 |
rs577392158 | snp | C/T | 1.88881e-05 | 0.00307306 | intron-variant | LYST | GRCh38.p7 | 1:235716821 | TAAATATTTTGATAC[C/T]GTCAAGATTAAGCTC | 1130 |
rs577421969 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865732 | GCTTAAAGTCAACAT[C/T]TTTATTAGCATAGAT | 1130 |
rs577424805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235846841 | AAAGAAAAAAGAATA[C/T]GAAAATATGAACAAA | 1130 |
rs577449320 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYST | GRCh38.p7 | 1:235850897 | TTGGCATGGACGTGG[C/T]GAACAGGGAACACTT | 1130 |
rs577523439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235844979 | GAGCTCCTGGGATCA[C/T]GGCGAAGGGAGGCAG | 1130 |
rs577531396 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235680099 | TTAAAATATATACTT[A/G]TAAGTTATATTAAAA | 1130 |
rs577555747 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858655 | CTTAATAAGCAGGAT[C/T]CCTATGGCTCAACCC | 1130 |
rs577563448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235709884 | CTACTAAGCATTCCT[G/T]TAGATAGCAAAATTA | 1130 |
rs577566641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235688856 | TGGGTGTGGTGGCAC[A/G]CACCTGTAGTCCCAG | 1130 |
rs577568111 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235674597 | CGTTTATTATAATCA[A/G]CAGTGGTTTGCTAAC | 1130 |
rs577575315 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853311 | AGGGTTAAGAATTGG[-/C]TCTGAACTAGATGTT | 1130 |
rs577582331 | in-del | -/TTTTG | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235722480 | AGCACTGAGCAAGTT[-/TTTTG]TTTTGTTTTGTTTTG | 1130 |
rs577606781 | snp | C/G | | | missense | LYST | GRCh38.p7 | 1:235697156 | TCTGGTGGGCAGAGC[C/G]TGGAGAGAGCCAAAT | 1130 |
rs577607440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235815761 | ACAATGAGAATTACA[A/G]AACATTGCTGAAAGA | 1130 |
rs577611523 | in-del | -/T | 0.420255 | 0.183066 | intron-variant | LYST | GRCh38.p7 | 1:235859502 | CCTGAGCACCAGGCC[-/T]TTTTTTTTTTTTTAA | 1130 |
rs577645888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235816232 | AGATCACAAGGTCAG[A/G]CGATTGAGACCATCC | 1130 |
rs577650915 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235829649 | ATCTGTAAAAGAAGG[G/T]TAGATGAAAACATCT | 1130 |
rs577665556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235707216 | TCCTAACCCCCTTCA[C/T]CCTATTTGAGTCTTA | 1130 |
rs577675111 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235863461 | AGAATGACTCTGTCT[-/A]AAAAAAAAAAAAATG | 1130 |
rs577686607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235829999 | CATAGTATATATGAA[A/G]CCATTTAGTTCTTAG | 1130 |
rs577688164 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235821453 | CCTGCCTCGAAAAAG[-/A]AAAAAAAAAATTGGT | 1130 |
rs577691253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235785866 | TACAGGCTAAAATTT[C/G]ACATTAAGATATTCC | 1130 |
rs577715014 | in-del | -/GA | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235843139 | GGTCCCTAGGTGGCT[-/GA]GTTTCCTTTTCAATA | 1130 |
rs577724698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235756214 | TTCTCCCCTTCAATG[A/G]CTCTCACAGTAGTGA | 1130 |
rs577734271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235806888 | TACTAACCACTACCT[A/T]ATTTTATTCATCAAT | 1130 |
rs577758365 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235858566 | TTTCCATTAATCCTG[A/C]ACTTGACTCATTTAG | 1130 |
rs577775413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYST | GRCh38.p7 | 1:235807453 | GATTCAGGTTGTCCA[C/T]GAATACGCCAAAGAG | 1130 |
rs577799191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235792358 | CTCACTCTGTTGCCC[A/T]GGCTGGAGTGCAGTT | 1130 |
rs577800247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682548 | GTATCAGACAACCTG[C/G]GGCTGGAACACAATG | 1130 |
rs577801869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235859156 | ACCCCATTTCCTTTT[C/T]GTTTTTAAACAGGAA | 1130 |
rs577802552 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684799 | ATTTTTTTATTTTTG[-/T]TTTTTTTTTGGTAGA | 1130 |
rs577803584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235687251 | TGAGCCAAATGTCTA[A/C]ATGTTGTTTCCAAAT | 1130 |
rs577824275 | snp | A/T | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235801542 | ATAAGTGAGAAACAG[A/T]CTCTGTCTTATTGAA | 1130 |
rs577836248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235791510 | AAAACTAAAGTTTCC[A/G]TAATAGAGATTCAAG | 1130 |
rs577836983 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235822896 | AGAAGCCATGTGGAT[A/G]AGAACTGAGGCTGGC | 1130 |
rs577854258 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LYST | GRCh38.p7 | 1:235871396 | GTTGGTCACAAGACA[C/T]TTATGGTTGAGGGAA | 1130 |
rs577877388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235835793 | CAAACTACATAGACA[C/T]ACCCTGTAGTTACTT | 1130 |
rs577926206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828712 | TTTAAAGAAGACAAA[A/G]CATTGAATTTTTTTA | 1130 |
rs577933468 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828781 | ATCAAAATTTCAAAA[-/T]AAATCACTATACATG | 1130 |
rs577940401 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LYST | GRCh38.p7 | 1:235777646 | ATACCAGGCACTATT[C/G]TAAGCACTTAAAAAT | 1130 |
rs577943588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235680274 | TTGTTTTTGTTTTTT[A/G]AGACAGGGTCTCACT | 1130 |
rs577951947 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714973 | GTGAATTGCATTTTT[A/C]TAAACTTAGACATTT | 1130 |
rs577966607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235793673 | GAGGAATAAATGAGC[A/C]ATTTCACCAAAAGAG | 1130 |
rs577969919 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235783254 | GTTTCACATATAACA[C/T]ATAAACTTAACTATT | 1130 |
rs577973358 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769114 | CAAACTGTATGTACA[C/T]AGTGTATAAAGGGAA | 1130 |
rs577983741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235723431 | AACACACCAAGGAGG[C/T]GTCTGCAACCAAGAC | 1130 |
rs577984667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866443 | CCCAGCTGGGCTGAG[C/T]AGTGCAGCGGCACAG | 1130 |
rs578000636 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867144 | GGCGGGCCGACCCGC[A/G]GGGCTGCAGCCGGGG | 1130 |
rs578012371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235715631 | CTACCTAACTTTGAG[A/C]ACTCCACCTCCTAAC | 1130 |
rs578052367 | snp | C/T | 1.65348e-05 | 0.00287526 | intron-variant | LYST | GRCh38.p7 | 1:235770335 | ATAAGCACATACTTA[C/T]TGAAAAATATGCAGC | 1130 |
rs578065435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235665943 | AGCGGTTAGGAGGCA[C/T]GATAAAGTTTGATGA | 1130 |
rs578074665 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718658 | AATATTTGGAGTCCA[C/T]TTTTCTTTAAACTAA | 1130 |
rs578078343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235673888 | ATGCCTGGCTGAAAT[C/G]GATTAAATATTCCGC | 1130 |
rs578095468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235814296 | AGTAGACAGTAAATA[C/T]ATAGATCTGGAACTT | 1130 |
rs578114703 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LYST | GRCh38.p7 | 1:235693918 | GGAAGCAACACCTAG[C/T]CTGAGAAGGGATCAT | 1130 |
rs578128191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235693294 | CGCTCCAGCTTGGGC[A/G]GCAGAGTGAGACTCC | 1130 |
rs578140015 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235792869 | GGGTTTCATCATATT[A/G]GTCAGGCTGGTCTCG | 1130 |
rs578158577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235834035 | AAAGGTTTTCAACTC[A/C]GAGTTCCTAGGTACA | 1130 |
rs578168847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235771134 | TCTCTCTTTATAAGA[C/T]AGAGCCAAGATATTC | 1130 |
rs578171871 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235730203 | TCAGTTTTTCATCTA[G/T]GAAATGGGTATAATA | 1130 |
rs578180909 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235680891 | GGCGTGAGCCACCGC[A/G]CCTGGCCTACAAGTG | 1130 |
rs578235329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738797 | AAGTATAATGAAGAA[C/T]CTTAGGCGGGTGCAC | 1130 |
rs578241546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235732001 | CATTTTTAGAAATAA[A/G]TAAGAGAAAAAAATA | 1130 |
rs578262648 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235747098 | TGGAATTCAATGCTA[C/T]AAAAGCATTTCCTGA | 1130 |
rs745327572 | snp | A/G | 1.65515e-05 | 0.00287671 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781964 | CAGGTCCCATTTTCC[A/G]GCCAACTGCAAAAAC | 1130 |
rs745329747 | snp | A/G | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660572 | AGTACAAAAACCACA[A/G]TAAGAAATGAAAGTT | 1130 |
rs745339578 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235864022 | CAGGTAATGTCTGAT[A/C]GCCCTGGCCTGTCTT | 1130 |
rs745350977 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704618 | GTTTTTTTCTTATAC[A/G]TTTGTTTAAGTTCCT | 1130 |
rs745353162 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235862524 | CCCAAGGCCGGGTGC[A/G]GTGGCTCATGCCTGT | 1130 |
rs745358946 | snp | A/G | 3.30715e-05 | 0.00406628 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716715 | AACAAAAGCTACCTT[A/G]TATGTGTCCACATAA | 1130 |
rs745373967 | snp | G/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810294 | TTCATTGCTATGCCT[G/T]TTTCATCTGAATTGG | 1130 |
rs745434558 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235836167 | TACACAAACACTGAT[C/T]TAATGTATTAGCTAC | 1130 |
rs745436754 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789338 | CATAATTTATATTCC[C/T]TGGTGAGTAGTTTTT | 1130 |
rs745446281 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235876351 | CACAGTATTTCTATT[C/G]TTATTTTCTTTAAAA | 1130 |
rs745448943 | snp | A/T | 3.36366e-05 | 0.00410088 | intron-variant | LYST | GRCh38.p7 | 1:235715392 | CAGAGAATTCATGAT[A/T]GTGGGCTCCAGGCAA | 1130 |
rs745463198 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235677251 | CATTCTCTTATTTTG[-/T]TAATTCTTCTTCTCA | 1130 |
rs745470755 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727012 | TAATTGCTATATAAA[A/T]GAGAAAAGAATGCTG | 1130 |
rs745471748 | in-del | -/AA | 1.67983e-05 | 0.00289808 | intron-variant | LYST | GRCh38.p7 | 1:235664437 | CTTATGAATGAAATC[-/AA]AAAAAGAGAATCCAA | 1130 |
rs745478659 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235821160 | ATATTATTGGCATCT[C/G]AGCATGGTGGCTCAT | 1130 |
rs745483295 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | LYST | GRCh38.p7 | 1:235697122 | GAAGACAGAAATTCC[A/G]TGACAAACCACAGAT | 1130 |
rs745510888 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235784931 | TTAGGCTTCAATTAC[A/G]TATTTTTACATTTTT | 1130 |
rs745513819 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759174 | CCTTTAGGTAATCAG[A/G]TCGGCGTGGGCAGGA | 1130 |
rs745519712 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235836938 | CTAGTGAATCAATTT[C/G]GGAATCATCAGGATA | 1130 |
rs745525685 | snp | C/T | 2.53142e-05 | 0.00355759 | intron-variant | LYST | GRCh38.p7 | 1:235782119 | ACAAAGTTAAAGCAA[C/T]GACTTTAGGAAGTCT | 1130 |
rs745529275 | snp | A/T | 6.61408e-05 | 0.00575031 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773908 | AACATCTTGGATTAT[A/T]GCATTAGAGTCTACA | 1130 |
rs745533707 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875299 | CACTATTCCCTATTT[C/G]CTCCTTTCATTTTTA | 1130 |
rs745541443 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235680536 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCATGAAC | 1130 |
rs745556242 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235728621 | GCCTCCAACTTTTTC[C/G]TGTTTCATAGGCTGG | 1130 |
rs745561765 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884671 | TTTCCTCCTCCTGTT[A/G]TTACCTTTAAAATAT | 1130 |
rs745562468 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235710650 | CCTTCCAGAATCTTG[C/T]TACTCTCCATCACAA | 1130 |
rs745595213 | in-del | -/TC | | | intron-variant | LYST | GRCh38.p7 | 1:235781453 | AGTCAATAAACACTG[-/TC]TGAATGCTATTATGT | 1130 |
rs745607617 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822309 | ATAATTATATTCCCA[A/G]ACCCTAGAACAGGGG | 1130 |
rs745613795 | snp | A/G | 1.66272e-05 | 0.00288328 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775066 | TGCTTGAGTTTCTTC[A/G]CAGCTACTGAGTTCA | 1130 |
rs745631177 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669377 | TAACTTTCCAGGCCT[A/T]AAGAACAAAAGGACC | 1130 |
rs745648405 | snp | A/G | 1.66313e-05 | 0.00288364 | synonymous-codon | LYST | GRCh38.p7 | 1:235664620 | GTCACTGCCTCCGCC[A/G]GCTAAAACACCCAAA | 1130 |
rs745656626 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235855574 | AAGCATGATAGTTTT[C/T]CATACCTCCTGAGGA | 1130 |
rs745683698 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809079 | CAACAGCATATTCCA[A/G]TGTTATGAACACCCG | 1130 |
rs745683957 | snp | C/T | 2.58602e-05 | 0.00359575 | intron-variant | LYST | GRCh38.p7 | 1:235806808 | GTAAAAAGGTTTAAA[C/T]AAAGAAACATCATTT | 1130 |
rs745696280 | snp | A/C | 6.62295e-05 | 0.00575416 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741478 | GATTTGGTTCATGAA[A/C]TATTTCAAAAATTTG | 1130 |
rs745703349 | snp | C/T | 1.67826e-05 | 0.00289673 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752143 | GCTGTATATCACAAG[C/T]AAGCAATTTATATTC | 1130 |
rs745719016 | in-del | -/AT | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884770 | GAAACTTTTGTACAT[-/AT]ATATATATAAACAAT | 1130 |
rs745742968 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854133 | GATGATGATGATGAT[A/G]ATCTGGCTAACACCT | 1130 |
rs745746960 | snp | C/T | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715269 | AGCACAGTGCCGCTA[C/T]TGGAATAGTGGGAGC | 1130 |
rs745751302 | in-del | -/ATAA | 1.66186e-05 | 0.00288254 | intron-variant | LYST | GRCh38.p7 | 1:235803067 | CAGATTGATGACTCT[-/ATAA]ATCAGTGTAATTCAA | 1130 |
rs745759850 | snp | A/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731073 | AGATACTTATTTGGA[A/T]TAGTTAAATAACATC | 1130 |
rs745774694 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837035 | GGAGCTTTCTGAGAC[A/G]ATGAGCCTGTTCTAT | 1130 |
rs745776792 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804650 | TTTCAAATAATATAC[-/T]TTCCACAGACAAGTT | 1130 |
rs745789615 | snp | C/T | 3.31422e-05 | 0.00407063 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762792 | TAAGGGACCTTCCTC[C/T]ACTGCTGGAATGCCT | 1130 |
rs745802943 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235810963 | CAGCCTGGCCAACAC[A/G]GTGAAACCCTGTCTC | 1130 |
rs745806176 | snp | A/G | 1.66396e-05 | 0.00288436 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762706 | GGTCATACTTCCATT[A/G]TTGCTATTTTTACCT | 1130 |
rs745820877 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687327 | GTGGATATATGTGTA[C/T]ATATATTTAGATAAA | 1130 |
rs745822776 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730927 | AAACAGGTAAGAGAG[C/T]GGTGGTTTGACAACA | 1130 |
rs745836523 | snp | A/C | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867677 | CCCGGCTCTGGGCCC[A/C]GCACGCTGCTGGCAG | 1130 |
rs745846104 | snp | C/T | 1.66463e-05 | 0.00288494 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741588 | CAAGACCACAGAATT[C/T]TAGTCCATTGCTGCT | 1130 |
rs745858981 | snp | A/C | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738054 | AAGGAAGAACAGATC[A/C]TCCAGAATAAGATTA | 1130 |
rs745863011 | snp | A/C/G | 4.96959e-05 | 0.00498456 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792055 | TGCAGTAAAGGGAAG[A/C/G]TTAGATACTGTGAAG | 1130 |
rs745892924 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235796341 | AAACAGCATAAAGAA[C/T]GGGAGAAAATATTTG | 1130 |
rs745927782 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720847 | GCGGTGATGTTACCA[C/T]ATTCCAGAAGATTAG | 1130 |
rs745941758 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235688425 | TTTTGGTTTTCTTAT[C/T]GCATTGTCCAAAGTA | 1130 |
rs745945442 | in-del | -/AATAT | 4.03828e-05 | 0.0044933 | intron-variant | LYST | GRCh38.p7 | 1:235755692 | AATGCATTAAAATTA[-/AATAT]AATATATACAAATCA | 1130 |
rs745947151 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717141 | AAGTTAGTGTCCCAT[A/T]TTCCAGACTCTACAT | 1130 |
rs745951888 | in-del | -/A | 1.80205e-05 | 0.00300165 | splice-donor-variant | LYST | GRCh38.p7 | 1:235774911 | ATTTTATGAAGACAT[-/A]CCTTCAAAATGTAAA | 1130 |
rs745953829 | snp | G/T | 1.65002e-05 | 0.00287225 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809404 | TCACACTATTTATTA[G/T]GGCTTTCAAATGCTC | 1130 |
rs745960300 | snp | C/T | 1.70761e-05 | 0.00292194 | intron-variant | LYST | GRCh38.p7 | 1:235810566 | AGAAGGCTTAGAATA[C/T]CTCAATATGTTTTAA | 1130 |
rs745961642 | snp | G/T | 1.68216e-05 | 0.00290009 | intron-variant | LYST | GRCh38.p7 | 1:235687088 | TATCATGTTTTAAAA[G/T]AATGAAACTTAAAGT | 1130 |
rs745971703 | snp | A/T | 1.64825e-05 | 0.00287071 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806241 | GATCCAACGACACAT[A/T]GACCAAATGTCTGCT | 1130 |
rs745977937 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235832130 | TACCAGATGGTATCA[C/G]CAGAAAGTTTCAGAA | 1130 |
rs745989710 | snp | C/G | 1.65792e-05 | 0.00287912 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235758987 | CTGTGAGCACTTGCA[C/G]TTCGGTTGTAATTTG | 1130 |
rs745997173 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235713925 | ATAATAGTAACATGA[A/C]TAAAAATATTGATAA | 1130 |
rs745998392 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878680 | TCCTGCCAAACCCAT[A/G]GCACCATTTTTGGAA | 1130 |
rs746005251 | snp | A/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733685 | TGAATCCAGACGCTG[A/T]AAGAGACTAAACAAA | 1130 |
rs746017828 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235675390 | ACTCCAGCCAATGGC[A/G]AGAGGATACAGCAAC | 1130 |
rs746024404 | snp | C/T | 8.51636e-05 | 0.00652492 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752025 | GTCCTCTTGTTTTTG[C/T]TATTTTGAAGATATC | 1130 |
rs746033288 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706404 | TATTCCCCTGGTTAA[C/T]CACACTTAGCTCCTA | 1130 |
rs746034273 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235846746 | CTCTGGAAAGTCTCA[C/G]CGATAGAACTAAACA | 1130 |
rs746055858 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702807 | AAACTGCACTAGCAA[C/T]CCCACAGCAGCTGGA | 1130 |
rs746059919 | in-del | -/GGGTTCTCTTGGCTC | 3.29908e-05 | 0.00406132 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746415 | TCAGTTGCTTGGCTA[-/GGGTTCTCTTGGCTC]GGGTTCTCTTGGCTC | 1130 |
rs746069548 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818677 | TTTGGCATATCTTTC[C/T]GGTAGAGTCCTCCTA | 1130 |
rs746071022 | snp | A/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853584 | CAGAAAGGTGTACAT[A/T]TTATTTTTTCATATT | 1130 |
rs746093835 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675826 | CTTCTAGTGTCACAA[C/T]TGAACTGCATGGTGG | 1130 |
rs746098369 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235707741 | ATTTTAATAGCAAAC[A/C]AATCCTAACTAAATA | 1130 |
rs746118990 | snp | C/T | 0.00014858 | 0.00861788 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751351 | CTCTAAGCTGTAGTG[C/T]AACAGCCATATCTAA | 1130 |
rs746129138 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845235 | GAGAAGCTGAAGGTC[C/T]GTTTGCTGGAGAAGT | 1130 |
rs746135438 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235823143 | CTTCAATCAGTCTGG[-/G]TGGATAATTGGGGGA | 1130 |
rs746137470 | snp | A/G | 1.67911e-05 | 0.00289746 | intron-variant | LYST | GRCh38.p7 | 1:235801135 | TTACTTGTATTCCCT[A/G]AACACTAAATATTTC | 1130 |
rs746156651 | snp | C/T | 1.66288e-05 | 0.00288343 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788738 | GGGGATCAGCCCACA[C/T]TTGGATCATCAACGC | 1130 |
rs746165198 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235804787 | ATTTGCAGTTGATAT[G/T]AAAGCAAAATGACTA | 1130 |
rs746169681 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734533 | ATGCACTGGGAGGGA[C/T]GCACTTGTGACCACA | 1130 |
rs746169989 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235812506 | AGTGAGACTCTGCCT[-/A]AAAAAAAAAAAAAAA | 1130 |
rs746187876 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235666033 | TGTCTTTTATTAAGA[C/T]AATGAAAATATTTCA | 1130 |
rs746189811 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791931 | ACTCTCTCTATCAGC[C/T]TCTTTCTTGCTCCGT | 1130 |
rs746203566 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777256 | CTAATCACTGGTTCA[C/T]AGATGGTATACTGAG | 1130 |
rs746204440 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235873147 | AGCATGCCAAGGCAC[C/T]AAACTTTGGGGTATT | 1130 |
rs746206938 | snp | C/T | 1.64936e-05 | 0.00287168 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810094 | TAACAGACAAGGCAG[C/T]TGGCTCACTTAAAAT | 1130 |
rs746209444 | snp | C/T | 1.69591e-05 | 0.00291191 | synonymous-codon | LYST | GRCh38.p7 | 1:235712109 | CTCTGGGATAAGTTC[C/T]TTCACATCAGTCATA | 1130 |
rs746224282 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | LYST | GRCh38.p7 | 1:235677538 | TTATCAGTATACTGT[A/G]TGGTTTGCAAACAAA | 1130 |
rs746228133 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858898 | CAGGCTGCTGGAGAA[C/T]ACTGCTTAACCATCC | 1130 |
rs746237892 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868159 | CTCTGGCAGGTAGTC[-/TT]TTATTTTTATTTTTT | 1130 |
rs746248700 | snp | C/T | 1.66109e-05 | 0.00288187 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809956 | GGAATTCAGTTAGTG[C/T]GGGCACTACACTGGC | 1130 |
rs746252504 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746957 | TGTTGTTGAATTTCA[G/T]AAAGTAGTTTTAAAA | 1130 |
rs746279511 | snp | A/G | 1.65176e-05 | 0.00287376 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753248 | TTCTGAAACAATCCC[A/G]TGTTTCTCACATCTT | 1130 |
rs746290921 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697932 | GGGGGAAGAAAGGTG[A/G]GTGAAGACTCTAGAG | 1130 |
rs746297204 | snp | A/G | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235729601 | TTTGACTTACCTAGT[A/G]ACAATTCACCAGCTG | 1130 |
rs746299176 | snp | C/T | 1.70368e-05 | 0.00291858 | missense | LYST | GRCh38.p7 | 1:235709273 | GGTTGACGTGATTAA[C/T]CCGTTCACCATTCTG | 1130 |
rs746323043 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235665425 | GACCAGCCTAGTTAA[A/C]ATGGTGAAACCCCAT | 1130 |
rs746323271 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | LYST | GRCh38.p7 | 1:235686904 | AGGCTTTCTTCCCCT[C/T]ATTGACAAAGTCCCA | 1130 |
rs746327422 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235798481 | GTCTATTAATAAAAA[C/T]TGAAGGAGAATTGCT | 1130 |
rs746335054 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693177 | AAAAAGTCAGCTGGG[C/T]GTGGTGGCAGGTGCC | 1130 |
rs746340392 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235733015 | AAATATCCTATTATC[G/T]TCTACTTTATAAACT | 1130 |
rs746343361 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235791660 | ATTATAGTCTGAAAA[C/T]AATCTTTGTGTACAA | 1130 |
rs746352044 | snp | C/G | 1.6671e-05 | 0.00288708 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766246 | CTACAAACCTCTCGG[C/G]GCATGGGTGTGAGTT | 1130 |
rs746352958 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771174 | AAGCCACACGAAAAC[C/T]AGCAGACAAGGCAGC | 1130 |
rs746374310 | snp | A/G | 3.88139e-05 | 0.00440516 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780884 | AAGAGACCAATATCC[A/G]CATCTTTCTTGGTCA | 1130 |
rs746374832 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826357 | TTTATTCATAATAGC[C/T]AAATGCATACAGCTC | 1130 |
rs746375196 | in-del | -/ATCTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235756005 | TCTCTGCAAATCTAT[-/ATCTAT]ATCTATATCTATATC | 1130 |
rs746380562 | snp | A/G | 4.94385e-05 | 0.0049716 | intron-variant | LYST | GRCh38.p7 | 1:235755463 | CAATTATAGTGGAGG[A/G]AAGAACACACTTACT | 1130 |
rs746387704 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235671779 | GTCCTTATAGCCTGG[C/T]GTAGATATGTAAATG | 1130 |
rs746394192 | snp | A/T | 3.47072e-05 | 0.00416562 | intron-variant | LYST | GRCh38.p7 | 1:235744173 | CTTTGAATTGAAAAA[A/T]AGAATACAAAATTAG | 1130 |
rs746394428 | snp | A/C | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885459 | TGTGATCTTCTGGAT[A/C]AGAGTATAGCTAAAA | 1130 |
rs746417866 | snp | G/T | 3.3269e-05 | 0.00407841 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808916 | AATATTACAAGCTGC[G/T]TTTTTAATTTTTGGT | 1130 |
rs746419862 | snp | G/T | 3.30513e-05 | 0.00406504 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806156 | GTATTATCATAAATA[G/T]TAACTTATGGCATAC | 1130 |
rs746450195 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672454 | CTAGTATTCTGAAAG[C/G]CACCAGAAGAAAGTG | 1130 |
rs746462876 | snp | A/G | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827659 | TGGCTATTTATTTTC[A/G]CTCCAAAGGCACATC | 1130 |
rs746464862 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807263 | TGAAAATCTACGGAA[G/T]GCTCAGCATCACATG | 1130 |
rs746466637 | snp | C/T | 1.65255e-05 | 0.00287445 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773924 | GCATTAGAGTCTACA[C/T]CCAACTTAAACTCTC | 1130 |
rs746479086 | snp | G/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787282 | AGGTGAGTACTAAAT[G/T]TTGCCATTTGCTTGG | 1130 |
rs746482877 | snp | A/G | 1.70904e-05 | 0.00292316 | synonymous-codon | LYST | GRCh38.p7 | 1:235697266 | CTTTTATCCATGACA[A/G]AGGACTCTAAAATGA | 1130 |
rs746483043 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665194 | AACAAGGTAAAATAA[C/T]CATCTTTGTGTAATT | 1130 |
rs746483299 | in-del | -/GAG | | | cds-indel, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808824 | GGACTGGATAAACTT[-/GAG]GAGAGTTCAGCATCA | 1130 |
rs746492629 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235851797 | GTGATCAAATTCCTC[C/T]TGGAATTTAAAATGC | 1130 |
rs746505273 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837592 | AGATTGAGCCACCGC[A/G]TACCAGCCTGGGTAA | 1130 |
rs746510919 | snp | A/G | 1.67486e-05 | 0.00289379 | missense | LYST | GRCh38.p7 | 1:235663077 | CACAAGAAAATGTAA[A/G]GCTGTAAAAAAAAAA | 1130 |
rs746514617 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702313 | AGTTCCCCTTAGGTA[C/T]AAACCAAAACATCCG | 1130 |
rs746531909 | snp | A/G | 1.65067e-05 | 0.00287282 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809224 | CAGTCTCTTCAAATG[A/G]GTTTTTGGAAACCTG | 1130 |
rs746532699 | snp | A/C | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867161 | GGCTGCAGCCGGGGC[A/C]CGGTCTGGGTTTCTC | 1130 |
rs746535884 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235798425 | TCTTTATAATATCTG[C/T]TCAATTTCTCTGTAA | 1130 |
rs746536848 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | LYST | GRCh38.p7 | 1:235697163 | GGCAGAGCCTGGAGA[C/G]AGCCAAATCTTTCTC | 1130 |
rs746546261 | snp | A/G | 3.29701e-05 | 0.00406005 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751241 | CTTTTGAACTACTGC[A/G]TGATGGGGAGCAGAA | 1130 |
rs746554031 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762426 | CCAGAATGATGGTTT[C/T]AGGTAGACAGAAGAG | 1130 |
rs746565235 | snp | A/G | 8.25157e-05 | 0.0064227 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806443 | CAGAGGAATAGGTTT[A/G]TTGTGTTGATATGAA | 1130 |
rs746584758 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235689965 | CGGAAAGCATCTTTA[A/C]AGTTATTTGTTCATC | 1130 |
rs746595700 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235864600 | CCCCTACAACAAAGT[A/C]TATTCTCCATCCAGC | 1130 |
rs746601688 | snp | A/C | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728111 | AAGCATTATCTTCCA[A/C]AAAATACATTCCACA | 1130 |
rs746604940 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703578 | CAGCCATATTTTGTA[C/T]ATATCCACTTGATGG | 1130 |
rs746610625 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235850181 | ATAAAAATAGGCACA[C/T]AGACCAATGGAACAC | 1130 |
rs746625967 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235864364 | CCCACCAAACCTACT[-/C]CTCTCGTAAACCTAA | 1130 |
rs746634900 | snp | C/T | 8.24056e-05 | 0.00641841 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759393 | CTTTTTTCAGTGTGT[C/T]GGAACTCCCCAAAGA | 1130 |
rs746642163 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759324 | AGAGGACAGCTTCCA[C/T]TTCACAAACAGTTTT | 1130 |
rs746643795 | snp | A/G | 1.67225e-05 | 0.00289154 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804662 | TACTTTCCACAGACA[A/G]GTTCTAAGGTAAAAT | 1130 |
rs746673638 | snp | A/G | 8.24042e-05 | 0.00641836 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759391 | GCCTTTTTTCAGTGT[A/G]TCGGAACTCCCCAAA | 1130 |
rs746674750 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235795165 | AAGTGACAGTGCGGC[C/T]GACAATACAGGGATT | 1130 |
rs746675344 | snp | C/T | 4.98873e-05 | 0.00499411 | intron-variant | LYST | GRCh38.p7 | 1:235774014 | AAATTAGCATTAATA[C/T]AAGATGCATTAGTAA | 1130 |
rs746677901 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235834699 | AGGGCTTTGTGTGAA[C/T]TAGGAAAAAACATCC | 1130 |
rs746683443 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235876996 | GAATGGAACAGGTGA[C/T]TGTAAGCACAGCAGA | 1130 |
rs746687640 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235862614 | CAGCCTGGGCAACAC[A/G]GTGAAACCCCATGTC | 1130 |
rs746700871 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | LYST | GRCh38.p7 | 1:235663972 | AAGCATAAGAGGGGG[A/G]GAAGATCTTACCTGA | 1130 |
rs746702228 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235691821 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTT | 1130 |
rs746713698 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793470 | AGTGAAAGAATTTAT[C/T]AGTGAAAAATGTAAA | 1130 |
rs746719614 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235748210 | AACTGTGTGTATGTG[C/T]GAGTGCATGGCAATT | 1130 |
rs746728779 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235724930 | GTGATACTCTGGTTG[C/T]TCTGTTGTATGTGTC | 1130 |
rs746733357 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235783615 | TAACAAACCTGCACG[C/T]TCTGCACATGTATCC | 1130 |
rs746748206 | snp | A/G | 1.6902e-05 | 0.00290701 | intron-variant | LYST | GRCh38.p7 | 1:235715397 | AATTCATGATTGTGG[A/G]CTCCAGGCAACGCTA | 1130 |
rs746751530 | snp | C/T | 3.30022e-05 | 0.00406202 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806044 | TCCTTCATAGTTCTC[C/T]TAGGTTGAGAAATTC | 1130 |
rs746758379 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235678739 | TATTTCTTCTGTCTT[G/T]TCAGAAGTTACTACT | 1130 |
rs746794308 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235678014 | AATTTACAACTATCC[C/T]TCATTGATAGACACT | 1130 |
rs746802579 | snp | C/T | 3.6626e-05 | 0.00427921 | missense | LYST | GRCh38.p7 | 1:235709290 | CGTTCACCATTCTGA[C/T]GCACACCAAAATCAA | 1130 |
rs746803650 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805944 | ATGCTGTAACTCTAA[C/T]TTACCTAAACTGTCA | 1130 |
rs746805108 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235842830 | TGATATCTTAGCTCT[A/G]TTCCAGTTCTGTGAT | 1130 |
rs746819166 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235767158 | ATTGCTTATATCCTC[A/C]AATTCCATCTCCCCA | 1130 |
rs746821329 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235784701 | ATCTGTATAAAGTGC[C/T]TAATACAGTGCCTGG | 1130 |
rs746829669 | snp | C/T | 0.000115513 | 0.00759888 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808560 | TGAGCTGAAGTAACG[C/T]TTAGGTGTTGACAAT | 1130 |
rs746834024 | snp | A/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731087 | AATAGTTAAATAACA[A/T]CTCTGTAAACGTCTC | 1130 |
rs746840390 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235881439 | AAAAATAATAGGGGT[A/G]TGAATTACCATACCA | 1130 |
rs746850774 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235710542 | TGACATACGAGAGTC[C/T]CAGGGGAACACTGAT | 1130 |
rs746894835 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842022 | TTCTGGTGGTATGGA[A/T]TTTTTCAGCTATTTC | 1130 |
rs746894979 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235857274 | TGGTTGTGGATGTTG[A/C]AAATAAGTGAATTGA | 1130 |
rs746900657 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235879094 | CACTGTAACCTCAAA[C/T]CCCTGGGCTCAAGCA | 1130 |
rs746909270 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768496 | AAAGACTAAGTTCAT[C/T]TCTTTATAAACTTCC | 1130 |
rs746910382 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | LYST | GRCh38.p7 | 1:235787151 | ATTGACTAATGAAAC[A/G]TAACATTGTAACTGA | 1130 |
rs746911004 | snp | C/G | 9.91998e-05 | 0.00704202 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716723 | CTACCTTGTATGTGT[C/G]CACATAACGATCTTC | 1130 |
rs746924997 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676144 | AACAAAACACTCTTG[A/T]TTAGGTGATATATTT | 1130 |
rs746932886 | snp | A/C | | | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235808205 | GCTCAGTAAAAAATG[A/C]ATACATACATAAACA | 1130 |
rs746940319 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235698929 | TTGAGAAAAATGTGT[C/G]TGCTAAATTTTAGTT | 1130 |
rs746953241 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669342 | ACTCACTTCCTAGAA[C/T]TAAATTCAAAGGAAA | 1130 |
rs746954090 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822047 | CCCCACTAAGATTCA[C/T]AGGAAACTCACAACA | 1130 |
rs746956055 | snp | C/G | 1.66788e-05 | 0.00288775 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757291 | CTTACTTTAATAACA[C/G]CTTGTTGTATAGCTG | 1130 |
rs746958181 | snp | C/T | 0.00016533 | 0.00909053 | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747277 | AGTTGACCATAGGAA[C/T]CAAAATGATGTCTTG | 1130 |
rs747015454 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235750588 | TATATATATGTATGT[A/G]TGTATATCCTGTGTA | 1130 |
rs747020854 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793701 | GAGGTAAAATACTAT[C/T]GTCACTTTTTGAATG | 1130 |
rs747022808 | snp | A/C/T | 1.66297e-05 | 0.0028835 | missense, stop-gained, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808921 | TACAAGCTGCTTTTT[A/C/T]AATTTTTGGTGATAT | 1130 |
rs747025603 | snp | A/G | 3.36423e-05 | 0.00410122 | intron-variant | LYST | GRCh38.p7 | 1:235800276 | TTATCAACTTTTCAC[A/G]TAAAATAATTTCAGA | 1130 |
rs747060652 | in-del | -/TAC | | | intron-variant | LYST | GRCh38.p7 | 1:235822403 | TCCTGTCCCTCTTCT[-/TAC]TACAATTAACTTACT | 1130 |
rs747082361 | snp | C/T | 1.65173e-05 | 0.00287374 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809684 | CTGCAGTGTTTTCTT[C/T]TGTCTTGGTGCAAAA | 1130 |
rs747105463 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235737031 | AATCCCAAAAAACTA[C/T]AAAACAAACTGGAAA | 1130 |
rs747106803 | snp | C/T | 1.64931e-05 | 0.00287163 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662898 | GTCAACAAATCTAGT[C/T]TGGAGTTAAAGTGCT | 1130 |
rs747126689 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867732 | TTTCAAGGGCCACCC[C/T]CCTCACCTCCTAGTC | 1130 |
rs747132028 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235775342 | AGTAGCATTTTATAA[C/T]TAGTGATCTGAAGTG | 1130 |
rs747150428 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720902 | GGTATACATCATCAC[-/G]AACCTAAAAGGGAAG | 1130 |
rs747153180 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737956 | CCAACACCCGCCGGA[C/T]GTGCATTCTCGATTC | 1130 |
rs747158273 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235831712 | TTAATATTTTTGAAT[A/C]TTAGAAAGGAGAAAA | 1130 |
rs747159963 | snp | A/G | 1.73429e-05 | 0.00294468 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741626 | ACTGGCTTTACTTGA[A/G]CCCTAAAATCAATCA | 1130 |
rs747164600 | snp | C/T | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759123 | CTAGCCCAAGGCTTG[C/T]AATAGTGCTGTGGCT | 1130 |
rs747166047 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719342 | GTCCTTTTGACAAGA[C/T]CATATTAGTTTCCTC | 1130 |
rs747169050 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673706 | TACAGGCTTCTTTGA[A/G]ATGCGCTTTGTTTCT | 1130 |
rs747169405 | snp | C/T | 1.65707e-05 | 0.00287838 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777097 | AATATGCCAGTTCCA[C/T]CAATTTCGTGCAGAA | 1130 |
rs747178388 | in-del | -/TTT | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884790 | ATATAAACAATGGCA[-/TTT]TTTTTTTTTTTTTCA | 1130 |
rs747181119 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235881349 | TAATTACCTAAAATT[A/C]CTCCTTGGAAGTTTG | 1130 |
rs747183026 | in-del | -/AAG/AAGAG | 1.65625e-05 | 0.00287766 | intron-variant | LYST | GRCh38.p7 | 1:235755430 | AAGAAAAGAAAAGAA[-/AAG/AAGAG]AAAAGACAAAAGATT | 1130 |
rs747187701 | in-del | -/AA | 0.000968644 | 0.021986 | intron-variant | LYST | GRCh38.p7 | 1:235775089 | TGAGTTCAACAACCT[-/AA]AAAAAAAAATGGGTG | 1130 |
rs747195191 | snp | C/G | 1.66266e-05 | 0.00288323 | intron-variant | LYST | GRCh38.p7 | 1:235709065 | TATCTTATATAAATA[C/G]AGATTGTTTTAAAAG | 1130 |
rs747205018 | snp | C/T | 1.65839e-05 | 0.00287953 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762721 | ATTGCTATTTTTACC[C/T]TCATATGGTGAAGCA | 1130 |
rs747220662 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717459 | GAATGAATTCTCATC[C/T]CTCCAGGAATGAATC | 1130 |
rs747225680 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235816218 | AGGCCAAGGCAGGTA[C/G]ATCACAAGGTCAGGC | 1130 |
rs747227934 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830960 | TCTTATGACATATTT[A/T]AATCAAATAAAGGGT | 1130 |
rs747235656 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674274 | CATCCCCAAGCGGAT[A/G]TATGGTAGTATTGTA | 1130 |
rs747236869 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848528 | AATAACCAAGATCAG[A/G]GCAAAACTAAATGAA | 1130 |
rs747253254 | snp | C/T | 1.78519e-05 | 0.00298758 | intron-variant | LYST | GRCh38.p7 | 1:235791626 | AAGAACACTACCACA[C/T]TTTTACGGCTCAAGG | 1130 |
rs747260083 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705380 | TATTTCAGTCTTCAG[A/T]TACTTTTTTTTAAAA | 1130 |
rs747266976 | snp | A/C | 1.69689e-05 | 0.00291275 | intron-variant | LYST | GRCh38.p7 | 1:235775094 | TCAACAACCTAAAAA[A/C]AAAAATGGGTGGATA | 1130 |
rs747272631 | snp | A/C | 1.65669e-05 | 0.00287805 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808450 | CCACCCACACACATA[A/C]AAACCTGGATTTAAG | 1130 |
rs747275377 | snp | A/G | 1.68852e-05 | 0.00290557 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752155 | AAGCAAGCAATTTAT[A/G]TTCACTCATGGGAAT | 1130 |
rs747280077 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235721532 | AAAAAACAGACAAGA[C/T]GAGCTTTGCTAAAAA | 1130 |
rs747281781 | snp | G/T | 3.29886e-05 | 0.00406118 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809051 | AGGAATGATTACAGA[G/T]TTGGGATCCATACAA | 1130 |
rs747290064 | snp | C/G | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662621 | AATCATAGAAAAAGG[C/G]GAGACCTTAATATTT | 1130 |
rs747319298 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806249 | GACACATAGACCAAA[C/T]GTCTGCTGCTTGGTG | 1130 |
rs747321030 | in-del | -/TATT | | | intron-variant | LYST | GRCh38.p7 | 1:235794364 | TTAAATACCACAAAC[-/TATT]TAGTTTGAACATTTT | 1130 |
rs747323601 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675015 | CTCTCGATTCTCCCC[C/T]GCCCTACTCAAATAA | 1130 |
rs747333053 | in-del | -/A | 1.64974e-05 | 0.00287201 | intron-variant | LYST | GRCh38.p7 | 1:235720636 | GGATGGATGAACCCT[-/A]AAGGTGATGATTCTT | 1130 |
rs747334123 | snp | A/G | 3.45381e-05 | 0.00415546 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781023 | GTCCACAAGCATACA[A/G]ATAAAAGGCCTCTTG | 1130 |
rs747344923 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818878 | GAGCTCTGCATGACA[C/T]AAGGTCCTTCCCACT | 1130 |
rs747370188 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706147 | AGCTCAAAAATCAGA[C/T]CCGAAGCCTTGCATT | 1130 |
rs747374741 | snp | A/C | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744074 | GAATATTTTCCTCAG[A/C]AATTTCGGTCTGGAA | 1130 |
rs747376348 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235706095 | ACCATGCCTGGCCTC[A/C]TAATTGCTTTTAAAG | 1130 |
rs747378283 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740347 | ATACATCCATTTAAC[C/T]ACTACTCAAAATAAG | 1130 |
rs747404117 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763178 | AGGGAGATTGTTCAT[C/T]CTTGAGGAAAGGACT | 1130 |
rs747407965 | snp | A/G/T | 6.60006e-05 | 0.00574428 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715208 | ATTCTTACCTTGATA[A/G/T]GCTAAAAACATTTTA | 1130 |
rs747414785 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733866 | GTTTTCTGCCAAGCA[A/G]CTTTATTCACTCCTT | 1130 |
rs747418238 | in-del | -/AAACTT | 3.46771e-05 | 0.00416381 | intron-variant | LYST | GRCh38.p7 | 1:235687093 | TGTTTTAAAAGAATG[-/AAACTT]AAAGTATAATAAAAA | 1130 |
rs747426872 | snp | G/T | 1.69885e-05 | 0.00291444 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813042 | AGAAGAGTCAGGAGT[G/T]CTTCTCTACATGTCA | 1130 |
rs747433731 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837292 | AGAAACCAGGTGAAG[A/G]AAGCTTGAAACAGAA | 1130 |
rs747449153 | snp | A/G | 9.89299e-05 | 0.00703244 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746398 | CTCTGCGCAAGTTCC[A/G]TTTCAGTTGCTTGGC | 1130 |
rs747453985 | snp | A/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720856 | TTACCATATTCCAGA[A/T]GATTAGGGAGGTTAT | 1130 |
rs747454684 | in-del | -/TC | | | intron-variant | LYST | GRCh38.p7 | 1:235843647 | TGAGGAAAATGATGT[-/TC]TGTTTCATAACGCTA | 1130 |
rs747463089 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235745909 | GAAAGTGGGTGTGGC[A/T]AAGAGAAGGGCAATA | 1130 |
rs747464150 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235872248 | TTGCAGTGAGCCAAG[A/T]TCGCACCACTGCACT | 1130 |
rs747469667 | snp | C/T | 1.65288e-05 | 0.00287474 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759067 | ATCAACAAGACTTGG[C/T]CAACGGCCAACAGCT | 1130 |
rs747487098 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860186 | CTTTTTTAAAAAAAG[A/C/T]CTTTATTTTTTAGAA | 1130 |
rs747489355 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235695157 | CAATAAGCATTTATT[A/C]AGCACTTAGAATGAA | 1130 |
rs747500733 | snp | A/G | 1.68001e-05 | 0.00289823 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746491 | CGCATTTTCATCAGA[A/G]GCGATTCAGTTTGAG | 1130 |
rs747510375 | snp | A/C | 1.65217e-05 | 0.00287412 | intron-variant | LYST | GRCh38.p7 | 1:235770315 | GAAGAGATAAACACA[A/C]ACCAATAAGCACATA | 1130 |
rs747517266 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235791234 | TTGCAGTGAGCCGAG[-/A]TCGCGCCATTGCACT | 1130 |
rs747536883 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873280 | AACCTCAGGCTGAAC[A/G]TGTCATAGTGTTCTA | 1130 |
rs747549132 | in-del | -/GTGTGTGTGTGTGTGTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235730599 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTAT]ATGTAAACTAACAAG | 1130 |
rs747555968 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235780018 | TACTGGTAGAACAAA[A/G]TATTGGAATAATATA | 1130 |
rs747566049 | snp | C/T | 3.42495e-05 | 0.00413807 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774933 | AAATGTAAAACCCAA[C/T]AATGCATTTTTGTTT | 1130 |
rs747570341 | in-del | -/CA | | | intron-variant | LYST | GRCh38.p7 | 1:235837624 | AGTGAGACCCTGTTT[-/CA]AAAAAAAAAAAAAAA | 1130 |
rs747579207 | snp | A/G | 1.65176e-05 | 0.00287376 | intron-variant | LYST | GRCh38.p7 | 1:235733706 | ACTAAACAAATAATA[A/G]GATTGTCCATAGTTA | 1130 |
rs747580992 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769859 | TAAAATTCATTAACT[A/G]TTCTTGCTGTTCAAG | 1130 |
rs747581162 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682079 | ACTTTGGGAGGCTGA[A/G]GCAGGAGGATTGTTG | 1130 |
rs747584162 | snp | C/G | 1.65839e-05 | 0.00287953 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235729654 | GATGCATCTTCGATT[C/G]ACTCTGTCAAAACAT | 1130 |
rs747587024 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801063 | TGGACTGCTTGATGC[A/G]CTGAAACCTTCTGTT | 1130 |
rs747587113 | snp | A/C | 6.5975e-05 | 0.0057431 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806323 | CATGGCAGCATATGA[A/C]TTAAAGGCTCGCTGG | 1130 |
rs747608805 | snp | G/T | 1.6612e-05 | 0.00288196 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809992 | AAGGAGAATTATGAT[G/T]CAAGGTAACGTCAAA | 1130 |
rs747622798 | snp | A/G | 2.11522e-05 | 0.00325202 | intron-variant | LYST | GRCh38.p7 | 1:235830436 | CGAGCTATAAAATAA[A/G]TATTACAAAAAAAAA | 1130 |
rs747640839 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235732765 | GTGAGGAATGTGTTC[A/G]TGCCTTTTGCTCATT | 1130 |
rs747647958 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235811339 | TTATATTCTCAAAAA[C/T]AGTATTCATAGACCT | 1130 |
rs747657797 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235704721 | GTTTACTCTATTGAT[-/A]AGTTTTTTTTCCTGT | 1130 |
rs747670195 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738511 | ACTCAGCCCAATTCC[A/G]TTACCCAATGGGGGA | 1130 |
rs747677876 | snp | C/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830369 | CATTGCAAAGCCGGT[C/T]GACATCGGTCAGAAA | 1130 |
rs747703566 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon | LYST | GRCh38.p7 | 1:235663986 | GAGAAGATCTTACCT[A/G]ATGATGGGCTTATTT | 1130 |
rs747718989 | in-del | -/GTC | 1.64909e-05 | 0.00287144 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810382 | GGGTAATTTTACGCT[-/GTC]GTCTGCTTTTTCGAA | 1130 |
rs747724553 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235842744 | GGAAATGAAATGGTC[A/G]CTAAAGTCAGTCAAC | 1130 |
rs747733863 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235825911 | TTAGACAACTTACAA[C/T]ATCTAATTTCCAAAC | 1130 |
rs747745727 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852891 | CAGAGTCCTATCCAA[C/T]GTTTTTCCTAATACT | 1130 |
rs747758257 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756191 | ACCAAATTAATCCTT[C/T]CACCTCTTTCTCCCC | 1130 |
rs747777620 | snp | C/T | 1.87732e-05 | 0.0030637 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780889 | ACCAATATCCACATC[C/T]TTCTTGGTCATAAAA | 1130 |
rs747781583 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235796998 | GTTGGCAAGAATGTG[A/C]AGAAATTAGAACCCT | 1130 |
rs747791415 | snp | C/T | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730867 | AGATTCACTTGCAGC[C/T]TTGTCTTTGACAGTA | 1130 |
rs747811333 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665418 | AGTTCGAGACCAGCC[C/T]AGTTAACATGGTGAA | 1130 |
rs747813418 | snp | C/T | 1.66474e-05 | 0.00288503 | intron-variant | LYST | GRCh38.p7 | 1:235753281 | AGATCAAATCTATAA[C/T]AAATAATACAGTTAA | 1130 |
rs747833182 | snp | C/G/T | 4.95596e-05 | 0.00497773 | intron-variant | LYST | GRCh38.p7 | 1:235787164 | ACATAACATTGTAAC[C/G/T]GAGATTGAGATGCAT | 1130 |
rs747835632 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235852068 | ATACTGAACTTGCTT[A/C]TCTGAAGAGTGCATT | 1130 |
rs747851915 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758188 | AAAGTTATGGGTCTG[C/T]GATAGCAGAAGTAGA | 1130 |
rs747863739 | snp | G/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791942 | CAGCCTCTTTCTTGC[G/T]CCGTGAAACTCGTGC | 1130 |
rs747867599 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797997 | TCAAACAAGATATAC[A/G]AATGGCCAATAAGTA | 1130 |
rs747869002 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235702224 | TATTTTGAAGTAAAA[A/G]TTATACCTACTTCCT | 1130 |
rs747936430 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689744 | CAATGTATATATACA[C/T]GTATTAAAACATCAC | 1130 |
rs747940128 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235834492 | ATCTGCCCACCTCGG[C/T]CTCCCAAAGTACTGG | 1130 |
rs747957831 | snp | A/T | 3.30355e-05 | 0.00406407 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806119 | TTTCCTTGCTCCTCT[A/T]TGTGACTTCTGAACA | 1130 |
rs747963986 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235782286 | CCATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 1130 |
rs747965164 | snp | C/T | 1.65018e-05 | 0.00287239 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810405 | CTTTTTCGAAAAACA[C/T]TTACTTTTGCAGAAA | 1130 |
rs747965676 | snp | A/C/G | 0.000219152 | 0.0104658 | synonymous-codon, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810533 | GAGCGGTAGGTTAAA[A/C/G]TCTAATGGAATGAAA | 1130 |
rs747988932 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687982 | AAAATGACTTTCTCT[-/G]ATCTTTATTCTTCTT | 1130 |
rs748026529 | snp | C/T | 1.65337e-05 | 0.00287517 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716726 | CCTTGTATGTGTCCA[C/T]ATAACGATCTTCTTT | 1130 |
rs748026551 | snp | C/G | 1.65693e-05 | 0.00287826 | intron-variant | LYST | GRCh38.p7 | 1:235733488 | GACAATTTTAACTGA[C/G]CTCCCGCAGCTTACC | 1130 |
rs748050010 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235783406 | ATAGTTTTAAATTTT[G/T]TATTTTAAAAAATAG | 1130 |
rs748080453 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235679791 | CCAGCCTTTTGGAGG[A/C/T]GGGCTCTCTTGGCAC | 1130 |
rs748092187 | snp | A/C | 3.33311e-05 | 0.00408221 | intron-variant | LYST | GRCh38.p7 | 1:235774036 | CATTAGTAATTGGTT[A/C]ATCAGGAAGTTCAAC | 1130 |
rs748106874 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751252 | CTGCATGATGGGGAG[C/G]AGAAGGTGACTGGAG | 1130 |
rs748108980 | snp | C/G/T | 3.29686e-05 | 0.00405998 | missense | LYST | GRCh38.p7 | 1:235709126 | TCGCTTGAACAGAAG[C/G/T]CTTCCCCTTTTGCTT | 1130 |
rs748128435 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881689 | GGAATATTATTCAAC[C/T]TTAAAAAGAAAAGAA | 1130 |
rs748130949 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235876571 | ACAGTTGCTAGAGCT[C/T]ATTATTATACTTGGG | 1130 |
rs748143582 | in-del | -/TAT | | | intron-variant | LYST | GRCh38.p7 | 1:235851432 | GGCGAGGGATTAAAA[-/TAT]GACTACAAATATGGT | 1130 |
rs748149337 | snp | A/T | 1.66985e-05 | 0.00288946 | intron-variant | LYST | GRCh38.p7 | 1:235758946 | TAAAATAAAGGTGGG[A/T]GGAGTGTACAAAAAC | 1130 |
rs748157775 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235843123 | CAACAGGGCAAGAAA[C/T]GGTCCCTAGGTGGCT | 1130 |
rs748159666 | snp | A/G | 3.29571e-05 | 0.00405924 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806581 | GAAGTACCCACATGT[A/G]CAGAGGACAACTCCT | 1130 |
rs748172494 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235833671 | ACAAAGCTTCACCTA[-/C]AAAAAAAAAGACATA | 1130 |
rs748175961 | snp | A/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787284 | GTGAGTACTAAATGT[A/T]GCCATTTGCTTGGGA | 1130 |
rs748179574 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820852 | AAAGTTTCTACATTA[C/G]TACTACAAATAGGAT | 1130 |
rs748199060 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698052 | AGAAAAGACATGATG[C/T]CCTTTTAAAGAGTTT | 1130 |
rs748199076 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710522 | CCTGACCCAAAGCAG[A/G]CAACTGACATACGAG | 1130 |
rs748210950 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667898 | TGATCTCCTGATCTC[A/G]TGATCTACCCACCTC | 1130 |
rs748233134 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670308 | AGGGATAAAAACTTT[A/T]CTCTCCTTTGTTTGG | 1130 |
rs748245362 | snp | C/T | 4.95291e-05 | 0.00497615 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808583 | TTGACAATGATGTGC[C/T]AATTCAACTCCTCTT | 1130 |
rs748261903 | snp | A/G | 4.97706e-05 | 0.00498827 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809798 | CATCATCTCTGCAGT[A/G]CTAACATCTACTGAC | 1130 |
rs748265106 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235750428 | GCATAGCATTGAACA[C/T]AGAAGTAGCTTAACA | 1130 |
rs748282945 | in-del | -/TTTG | | | intron-variant | LYST | GRCh38.p7 | 1:235706597 | GGGTTTTTGTTTTTC[-/TTTG]TTTTTGTTATTTTGC | 1130 |
rs748309102 | snp | C/T | 1.6612e-05 | 0.00288196 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753104 | TAGAGTAGACCATTA[C/T]CCAGCAACATATCTG | 1130 |
rs748317357 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685217 | GTCTGGATGTCCTTC[C/T]TCTGTGGTCCTCTAT | 1130 |
rs748320375 | snp | G/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828038 | CTCAACATCATTAGT[G/T]GTTAGAGGAATGTGA | 1130 |
rs748328211 | in-del | -/TCATTCAA | | | intron-variant | LYST | GRCh38.p7 | 1:235693971 | GTGTATGGTAGACCT[-/TCATTCAA]TCATTCAATTCAAGG | 1130 |
rs748331156 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735416 | TAGCCAATCTTTTAT[G/T]AACAGGCCCTAAAAC | 1130 |
rs748360219 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235696594 | GAAGAGGCCTCTACT[A/G]CACAGCACTTTCCCA | 1130 |
rs748372093 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835005 | CTGCAACAACCTCTG[C/T]CGCCTGGGTTCAAGT | 1130 |
rs748398280 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777225 | AGAGAGTTGGGTTTT[C/T]ATTTGACCTTTAAGT | 1130 |
rs748409576 | snp | G/T | 1.64882e-05 | 0.00287121 | intron-variant | LYST | GRCh38.p7 | 1:235677463 | GCTATGTTTGATTTG[G/T]AGACCTTCTTCTGTA | 1130 |
rs748414042 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235673617 | CATCTCTATTACTAT[A/C]CCTACCTCTAGCAAC | 1130 |
rs748419053 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718154 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCTGCAAT | 1130 |
rs748421660 | in-del | -/ACACATAT | | | intron-variant | LYST | GRCh38.p7 | 1:235857781 | CACACACACACACAC[-/ACACATAT]ATATATAAAATTTCA | 1130 |
rs748430581 | snp | C/G | 1.64841e-05 | 0.00287085 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734478 | CTATGGTTTCATTGA[C/G]TCACCTCTTTGATCA | 1130 |
rs748467127 | in-del | -/A | 9.94876e-05 | 0.00705223 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741384 | ACTTTGTATTTCACC[-/A]AACGTTTTACTTCTC | 1130 |
rs748493026 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235829406 | CCAATTTTACATCTA[A/C]AGCTGGTAACATTCA | 1130 |
rs748496334 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235881608 | AAGAAAATGTGATAT[A/G]TTATATATATCACTG | 1130 |
rs748498084 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235709688 | TAGAATCAAACTAAG[G/T]CTTTGTAGAAGCATT | 1130 |
rs748498238 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235679986 | AATGCTTTTAAGGCT[-/CT]CTCTCTCTCTCTCTC | 1130 |
rs748508598 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235719088 | CAGTGGTGCAATCTC[A/G]GCTCATCGCAACCTC | 1130 |
rs748510622 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687170 | TATTTTTTTTAACTC[C/T]CAAAAATGTTAGGTA | 1130 |
rs748519243 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | LYST | GRCh38.p7 | 1:235724004 | ACTTAAACAATATAT[A/G]TCAATTAATAAGGGT | 1130 |
rs748522992 | snp | C/T | 0.000109296 | 0.00739161 | intron-variant | LYST | GRCh38.p7 | 1:235830184 | AGCTACAGTTAACTA[C/T]CATATATTGATGAAA | 1130 |
rs748529967 | snp | A/G | 3.37143e-05 | 0.00410561 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759589 | TGGAATAATATTAGA[A/G]GAATTCTCTCCTGGT | 1130 |
rs748538643 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809133 | CTCAAGGAAGCCTGC[C/T]GTAGTAAGCGCAAGC | 1130 |
rs748540089 | snp | A/G | 1.64874e-05 | 0.00287113 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662923 | AGTGCTTTGGAGAAC[A/G]TGAAGTTCATTCGCA | 1130 |
rs748555313 | snp | C/T | 6.61376e-05 | 0.00575017 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724172 | TGGTTCCAACTCTCC[C/T]TGAAGGCTCTAAGAC | 1130 |
rs748563775 | snp | C/T | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235661004 | TTTGAGATCTGCTCA[C/T]AATATTTAAATAGCT | 1130 |
rs748576792 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806333 | TATGACTTAAAGGCT[C/T]GCTGGCTGTGCTGTC | 1130 |
rs748582423 | snp | C/T | 0.000121029 | 0.00777816 | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747170 | GCACCATTACTGCAC[C/T]TGCTCCAGGAGGTAC | 1130 |
rs748588206 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817417 | TACCATAAAGACAAA[C/T]GTGTGCTTATGTTCA | 1130 |
rs748588451 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821641 | ATTGCAACCTTTTTA[C/T]ATAAAGAACCAGATA | 1130 |
rs748598186 | snp | A/G | 3.4188e-05 | 0.00413435 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752168 | ATATTCACTCATGGG[A/G]ATGCTAAAGATAACA | 1130 |
rs748605237 | snp | A/G | 4.95176e-05 | 0.00497558 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733886 | ATTCACTCCTTCTTC[A/G]GTTTCATATTTCTTT | 1130 |
rs748611630 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674151 | CAATGTCAATTTTAC[C/G]TTGTGTCTCTCACGA | 1130 |
rs748622586 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740432 | CTTTCTCACCGTCCC[C/T]CTTCCACAGAGACAA | 1130 |
rs748634023 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704788 | TTGCTCTTGTTGTGA[A/G]TACTTTTTATAAACA | 1130 |
rs748636874 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705994 | GACAGGGTTTTGCCA[C/T]GTTGGCCAGGCTGGT | 1130 |
rs748643427 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235849659 | GAACTGATAAAAGAA[A/T]TCAACAAAGTTTCTG | 1130 |
rs748645846 | snp | A/G | 1.68863e-05 | 0.00290566 | intron-variant | LYST | GRCh38.p7 | 1:235791648 | GGCTCAAGGAAAATT[A/G]TAGTCTGAAAACAAT | 1130 |
rs748647939 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802043 | TACTAAAAATATAAC[A/G]ATTAGCTGGGCATGG | 1130 |
rs748654084 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235805574 | ATATATACATAAAAC[-/AT]AATATATACACATAT | 1130 |
rs748655415 | snp | C/T | 1.6522e-05 | 0.00287414 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809690 | TGTTTTCTTTTGTCT[C/T]GGTGCAAAAGGGTCA | 1130 |
rs748659198 | snp | A/C/T | 1.64939e-05 | 0.0028717 | LYST | 1 | allele_origin=A(germline)/C(germline) | 1:235759159 | GGAAGGAGGCCAATC[A/C/T]CTTTAGGTAATCAGG | 1130 |
rs748667700 | snp | A/G | 1.65263e-05 | 0.00287452 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235803000 | AAACTACAACACTGA[A/G]AATCCTCAGCTTCTT | 1130 |
rs748677619 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235735885 | AAAAATGAACAGAAG[-/CT]CTGTGAGTAAAAGGC | 1130 |
rs748680043 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750973 | TGTGTCTGTTTTTTT[C/T]ATCATTGTATCTCCA | 1130 |
rs748682228 | snp | A/G | 1.65165e-05 | 0.00287367 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792039 | GCTTAAATTTGGAGC[A/G]TGCAGTAAAGGGAAG | 1130 |
rs748687435 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235860735 | AAAGTGCATAATTTG[A/G]TATGTTCCAACATAT | 1130 |
rs748701858 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743827 | TAGCAATATATATTA[C/T]TCTATAATTAAAAAT | 1130 |
rs748702571 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235837037 | AGCTTTCTGAGACGA[C/T]GAGCCTGTTCTATAA | 1130 |
rs748728963 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235874946 | AAGCCCAGGCTCCTC[C/G]TCCAACCAGCAGCAT | 1130 |
rs748735840 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235803561 | TCTACATAACAAGCA[C/T]CTCAGAAGTCAAGAG | 1130 |
rs748736783 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785444 | AAGTGCTCAAAACAC[G/T]GTAATTCCTCAATAA | 1130 |
rs748737739 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785251 | CGTAAGTGTCAAACT[C/T]GATATTTTCTGCCTC | 1130 |
rs748739106 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235683301 | GTAATACTACCTTGT[A/G]TAAGCTGCACACATA | 1130 |
rs748741396 | in-del | -/AT | 1.64917e-05 | 0.00287151 | frameshift-variant | LYST | GRCh38.p7 | 1:235664050 | AGTCCCATGTGCTCC[-/AT]ATAACCTAGAGGGGA | 1130 |
rs748789807 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810199 | CTTTGGTTGCTAAGC[A/G]GTCAAGTTTAGCTTT | 1130 |
rs748796344 | snp | A/G | 1.6806e-05 | 0.00289875 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762681 | AGAATATTCAGAACT[A/G]AAATGAGAAGGTCAT | 1130 |
rs748806236 | snp | A/C | 1.64874e-05 | 0.00287113 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810122 | AATGTCAGTGTTTGA[A/C]CCCTGTCTTGGAATA | 1130 |
rs748823383 | snp | A/G | 1.65866e-05 | 0.00287976 | missense | LYST | GRCh38.p7 | 1:235664598 | CGTTCACCGTCCAGA[A/G]TCTGAGGTCACTGCC | 1130 |
rs748826930 | snp | A/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712894 | TCAGACTTTCTAGCC[A/T]TAGGGAAAGGCCTAG | 1130 |
rs748827565 | snp | C/T | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805792 | CTAGTTCTGGCACCA[C/T]GAAGACAAATGGCCA | 1130 |
rs748842989 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822476 | AACCTGTCTAATTCA[C/T]AAGTTTCTCAATCAA | 1130 |
rs748856241 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755490 | TACTCTTCATCAAGG[C/T]CAATATGTCGACCAA | 1130 |
rs748861372 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818637 | ATGTACATGGTCTTT[A/T]AAAAAAAAAAAAGAT | 1130 |
rs748908539 | snp | C/T | 0.000165079 | 0.00908363 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770163 | CATGAAAAGTACCTG[C/T]AAAACCTGACAAGTC | 1130 |
rs748933093 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809193 | CACCGCTCAGGATAA[C/T]AAACATCTCCATCTG | 1130 |
rs748942618 | snp | C/T | 1.65817e-05 | 0.00287933 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781949 | GAGAAGCAAATTTCC[C/T]AGGTCCCATTTTCCA | 1130 |
rs748942851 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769703 | ACAATGTAACTGATA[C/T]AATTAGTGTCACTTT | 1130 |
rs748953445 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235670290 | AGTAACAGGAGCTGC[A/G]TTAGGGATAAAAACT | 1130 |
rs748955859 | snp | C/T | 1.8039e-05 | 0.00300319 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781043 | AAGGCCTCTTGTGAA[C/T]CAACCTTAGCTCCTG | 1130 |
rs748972864 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235737467 | AACATACCTAGTCCT[C/T]AGATTTGTAGTCTCT | 1130 |
rs748978832 | snp | A/G | 4.94417e-05 | 0.00497176 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755587 | GCAAGGAAAATCCAC[A/G]ATTCTTCAGAAATTT | 1130 |
rs748985876 | snp | C/T | 1.64928e-05 | 0.00287161 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809060 | TACAGATTTGGGATC[C/T]ATACAACAGCATATT | 1130 |
rs748993738 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235714528 | GTAGTTCAAGAATGG[C/T]TGAGTAAAAGAATGG | 1130 |
rs748993774 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703216 | ATGTTTATAAAATTA[C/G]CTTTTAATTTAAGAT | 1130 |
rs748999960 | in-del | -/ACACACAC | | | intron-variant | LYST | GRCh38.p7 | 1:235666228 | GCAGTATGTACATAC[-/ACACACAC]ACACACACACACACA | 1130 |
rs749009748 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235770500 | AAATAGCTATGTTGA[A/G]TACAATATTGTATTA | 1130 |
rs749009959 | snp | A/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854006 | AACTATGAAGGTTCA[A/T]CCAGGTAAATCATCT | 1130 |
rs749030646 | snp | A/G | 2.40099e-05 | 0.00346473 | intron-variant | LYST | GRCh38.p7 | 1:235792162 | TGAAACTTTCTAATC[A/G]CGTAATAAAGTACAT | 1130 |
rs749037787 | snp | C/T | 3.29924e-05 | 0.00406142 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809376 | ACTTTTTTGACAGTG[C/T]TCATTATTTTCATCA | 1130 |
rs749041963 | snp | A/C/G | 3.29632e-05 | 0.00405964 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720834 | TAAATTTGTCAGAGC[A/C/G]GTGATGTTACCATAT | 1130 |
rs749043173 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671129 | TTTTAGTAGAGACAA[C/G]GTTTTGTCATGTTGG | 1130 |
rs749045467 | snp | A/G | 1.68778e-05 | 0.00290493 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788702 | AGGATAATCAATACC[A/G]AAAGATAAGAGTGGC | 1130 |
rs749060806 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700801 | GTGTCTATTATATGC[C/T]CAGGACCTTCCTAGG | 1130 |
rs749078855 | in-del | -/A | 3.36729e-05 | 0.00410308 | intron-variant | LYST | GRCh38.p7 | 1:235802859 | ACCATTTTGCTATTT[-/A]ATGATCTGGCTTGCA | 1130 |
rs749087595 | snp | A/C/G/T | 0.000115951 | 0.00761346 | missense, stop-gained, synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751350 | ACTCTAAGCTGTAGT[A/C/G/T]CAACAGCCATATCTA | 1130 |
rs749095304 | in-del | -/AA | 2.11642e-05 | 0.00325295 | intron-variant | LYST | GRCh38.p7 | 1:235781073 | GAATAGCAGAAAAAT[-/AA]AGTTAGTTATTTAAA | 1130 |
rs749110313 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866061 | AGATAAGAATTAGCG[C/T]TAAGGAAACGTTTCT | 1130 |
rs749145418 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235724489 | TCTATTATTAAATCT[G/T]GCATTTGGTGTGGGA | 1130 |
rs749157673 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235688496 | CACCACTTCTGTAGT[A/C]TACTTTTGGCTTTCA | 1130 |
rs749186542 | snp | C/T | 1.66067e-05 | 0.00288151 | intron-variant | LYST | GRCh38.p7 | 1:235830455 | TACAAAAAAAAAAGA[C/T]TAGGAAAACAAATAC | 1130 |
rs749190857 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235675476 | ATCGGTCGGTCGGAC[A/G]CAGGCAGCACCTTTC | 1130 |
rs749223189 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797747 | ATGACACCAAAGGTA[C/G]AGCAAACTAAATAAA | 1130 |
rs749227321 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832718 | TCTAGCTTTTTATTA[A/T]CATAAACAAAGCTAC | 1130 |
rs749238804 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832928 | CTGGTATATAGTAGG[C/T]ACATAGGAAGTGGAT | 1130 |
rs749242539 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878509 | CGCCCTGCTTCCGCC[A/G]TTGTGGTTCCTACTG | 1130 |
rs749243447 | snp | C/T | 1.67024e-05 | 0.0028898 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759571 | ATGGGCGGCCATCTG[C/T]TGTGGAATAATATTA | 1130 |
rs749277578 | snp | C/T | 0.00010585 | 0.00727419 | intron-variant | LYST | GRCh38.p7 | 1:235804693 | AAAAGAGACTAAGAA[C/T]ATTAATAACCATTTT | 1130 |
rs749282192 | snp | A/T | 0.000199097 | 0.00997541 | intron-variant | LYST | GRCh38.p7 | 1:235751999 | TTCATAAAAATTAAA[A/T]CTTACTTTGTGTCCT | 1130 |
rs749328823 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235834341 | TCCTTATCATAGTTA[C/T]GCGGCAAACATGAAG | 1130 |
rs749330732 | snp | G/T | 1.65625e-05 | 0.00287766 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766103 | AAGAAAAGTAGAAGT[G/T]CGTGGGATTGTGACA | 1130 |
rs749333802 | snp | C/T | 1.64814e-05 | 0.00287061 | missense | LYST | GRCh38.p7 | 1:235677508 | ATATGATGCAGGTTC[C/T]GTCTCTGCTCACACT | 1130 |
rs749337438 | snp | A/G | 0.000114475 | 0.00756469 | intron-variant | LYST | GRCh38.p7 | 1:235780830 | TACCTAAATACATTT[A/G]CTATAAAATTAAAAT | 1130 |
rs749347721 | in-del | -/AAT | 1.66319e-05 | 0.00288369 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744138 | AGTTCTCAAAATGTC[-/AAT]AATGTCTGAATTAAA | 1130 |
rs749353041 | snp | C/T | 1.65154e-05 | 0.00287358 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810431 | AGAAACCTGACTAGA[C/T]AGGGCACTTCCTTCT | 1130 |
rs749357238 | snp | A/G | 1.65449e-05 | 0.00287614 | intron-variant | LYST | GRCh38.p7 | 1:235733494 | TTTAACTGACCTCCC[A/G]CAGCTTACCTATCAT | 1130 |
rs749363982 | in-del | -/AG | | | intron-variant | LYST | GRCh38.p7 | 1:235877975 | CAACAGGGTGTTACT[-/AG]ATTCTAGAAATCTAA | 1130 |
rs749375615 | snp | G/T | 1.68326e-05 | 0.00290104 | intron-variant | LYST | GRCh38.p7 | 1:235677670 | CAACAAAAAGTACTC[G/T]AGTATAGTATCTCAA | 1130 |
rs749383468 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707784 | AGACTGCTAAATAAA[C/T]TATTCTATAGCTATA | 1130 |
rs749416238 | snp | C/T | 4.99164e-05 | 0.00499557 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808773 | AACAAATCTTCAGAT[C/T]CACTGCTGGGCAGGA | 1130 |
rs749419421 | in-del | -/TTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235856942 | ACAGGATATACTGAT[-/TTTT]TTTTTTTTTTTTTTT | 1130 |
rs749424368 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235666314 | GCATGCGAAAACATG[A/G]ATGAACCCTGAAAAC | 1130 |
rs749432149 | snp | A/C | 1.67576e-05 | 0.00289457 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744149 | TGTCAATAATGTCTG[A/C]ATTAAATTCTTTGAA | 1130 |
rs749457634 | snp | C/T | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806407 | GACTCTGCTTCTTTA[C/T]TTACGCATAAAAAAG | 1130 |
rs749462394 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858797 | TTTTCTGCATTGTTA[C/T]GGGGGTGGGGAAGGG | 1130 |
rs749482579 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235747163 | CATTCCTGCACCATT[A/C]CTGCACCTGCTCCAG | 1130 |
rs749485324 | snp | G/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801025 | ATTATTTCCCCTTGA[G/T]TGAGGTTTTCGAGTA | 1130 |
rs749491660 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787339 | CCTGTGCTAGTAAAA[C/T]AGCTTTCATGTCATC | 1130 |
rs749523287 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235733377 | AAAAAACATCACAAA[C/T]GATTAAACAAAAAAT | 1130 |
rs749553632 | snp | C/T | 8.24002e-05 | 0.0064182 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804515 | ATACCTTCTCAGTCA[C/T]AGCATCATTATGTTC | 1130 |
rs749568274 | snp | G/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826592 | AGGGGAGGGACTGAC[G/T]GAAAAAAAAGGCATG | 1130 |
rs749571960 | in-del | -/TT | | | intron-variant | LYST | GRCh38.p7 | 1:235861265 | GCCTTTTGAAAATTA[-/TT]TGATTCCTTTCTTGA | 1130 |
rs749583142 | snp | A/G | 3.31538e-05 | 0.00407134 | intron-variant | LYST | GRCh38.p7 | 1:235800832 | TTGGGTGATGAGTCT[A/G]ATAAATATTGATCAC | 1130 |
rs749585509 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791814 | CACATTAAACCACAG[A/G]GAAACACTGAAACCT | 1130 |
rs749601013 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235716988 | CCCACAGAGCCAGGC[A/C]AGTATTAGGAATTCC | 1130 |
rs749602554 | snp | A/T | 5.02795e-05 | 0.0050137 | intron-variant | LYST | GRCh38.p7 | 1:235791658 | AAATTATAGTCTGAA[A/T]ACAATCTTTGTGTAC | 1130 |
rs749641058 | snp | C/T | 4.95258e-05 | 0.00497599 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830349 | CTCCACCCTCTGGAC[C/T]ACTGCATTGCAAAGC | 1130 |
rs749661417 | in-del | -/TGTG | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662495 | TCCTCTTTTGGAGCA[-/TGTG]TGTGTGGTGGGAGGA | 1130 |
rs749667023 | snp | C/G | | | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235865080 | TTTATTTCTACTCCT[C/G]TTTGCTTTTTCCACC | 1130 |
rs749673503 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235792961 | GAGCCATGGCGCCCT[A/G]CCTTAGATGTTCTCT | 1130 |
rs749676628 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235741787 | TATCCATACACATAG[A/G]AGTTTAAAAGAGATG | 1130 |
rs749677074 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | LYST | GRCh38.p7 | 1:235663053 | TTGCTGTGTACAAAT[A/G]GTGGCCATCACAAGA | 1130 |
rs749679300 | snp | A/T | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806537 | TGAGACTCTGAGGAG[A/T]ATCTGAATAAGCTTG | 1130 |
rs749681115 | snp | A/G | 1.65285e-05 | 0.00287471 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235803023 | AGCTTCTTCTGAAAA[A/G]TCACCAGGCTGGGAT | 1130 |
rs749681929 | snp | A/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830297 | GGTACTGTCCAAGGG[A/T]TGCCATGTGCGTCTC | 1130 |
rs749703715 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235716549 | CAGAAAATCAGGATA[C/G]AAAATGATATTTCAT | 1130 |
rs749705699 | snp | A/G | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827868 | TACAAAGAAAATACC[A/G]TATTTGGAATCCAAT | 1130 |
rs749709074 | snp | A/G | 1.68015e-05 | 0.00289836 | synonymous-codon | LYST | GRCh38.p7 | 1:235709262 | CCAAGGGGGAAGGTT[A/G]ACGTGATTAACCCGT | 1130 |
rs749715458 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689808 | TCAATTTTATCCCAA[A/T]AAAGCTAGAAAAAAA | 1130 |
rs749724058 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235883088 | ACCAGTCACCTTTCT[C/T]GGTGGTACTTAAAGC | 1130 |
rs749726789 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734597 | GCCTAGCTCTTCTTC[A/G]GTCAATTCACCTTGG | 1130 |
rs749732470 | snp | G/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753216 | CTATTAGTCCCAGAA[G/T]AGGAATGACAGACCA | 1130 |
rs749746328 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718010 | CTGGGACTACAGGCA[C/T]GCACCACCACGCCTG | 1130 |
rs749761952 | in-del | -/AAAG | 1.65567e-05 | 0.00287716 | intron-variant | LYST | GRCh38.p7 | 1:235755433 | AAAAGAAAAGAAAAA[-/AAAG]AGACAAAAGATTCCC | 1130 |
rs749767171 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235774826 | TTCAGGAATAACTGA[A/G]ATACAAAACTATTAT | 1130 |
rs749771143 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235758474 | CCAATGTTCAGCACT[A/G]AGACCTGCATTATAA | 1130 |
rs749772244 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713484 | TATTAAACAGTACTA[C/T]TACAAATTCCCATTA | 1130 |
rs749776565 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881745 | TGAATCTTGAAGGTA[A/T]GCTGCTGAGTGAAAA | 1130 |
rs749778166 | snp | C/T | 6.59761e-05 | 0.00574314 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777233 | GGGTTTTCATTTGAC[C/T]TTTAAGTCTAATCAC | 1130 |
rs749786080 | in-del | -/AAC | | | intron-variant | LYST | GRCh38.p7 | 1:235825031 | TCTCAAAAAAAAGAA[-/AAC]AACAACAACAACAAC | 1130 |
rs749802560 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814278 | TAATGAAGACAGCTT[G/T]TTAGTAGACAGTAAA | 1130 |
rs749804968 | snp | C/T | 1.65938e-05 | 0.00288039 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808637 | ATTATATAATTTCCA[C/T]TGAACAACTATATTG | 1130 |
rs749813479 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791839 | AAACCTTCTGATAGG[C/T]GTGGCCAGCAGTTTT | 1130 |
rs749816627 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703703 | TTTCAGAAGTTAGGT[C/T]ATCTTCAACTCCATT | 1130 |
rs749857705 | snp | C/T | 3.32094e-05 | 0.00407475 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809916 | AAGTTGTCGCTCAGA[C/T]TGCAGCAGTCCCCAA | 1130 |
rs749911220 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687845 | GTCTGCTTTCAAGGT[C/T]AGCCTTGCCTCATCC | 1130 |
rs749914971 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674047 | ACCCCACAGCCCGGG[A/G]CAATAAGGCATGCCA | 1130 |
rs749923495 | snp | A/G | 3.31022e-05 | 0.00406817 | intron-variant | LYST | GRCh38.p7 | 1:235731221 | TAAGTGACCATCCAG[A/G]ACTTGTAGCTATAAA | 1130 |
rs749925644 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235689114 | AAATATATCTTTAGA[A/C]ATGTATCTCTAGATG | 1130 |
rs749926054 | in-del | -/AC | 1.65207e-05 | 0.00287404 | intron-variant | LYST | GRCh38.p7 | 1:235733726 | TCCATAGTTAAGCAT[-/AC]ACATGGAACGTATTT | 1130 |
rs749926904 | snp | G/T | 3.33034e-05 | 0.00408051 | intron-variant | LYST | GRCh38.p7 | 1:235677213 | AAAAGACATGAATTT[G/T]TATATGATCATTAAA | 1130 |
rs749934703 | in-del | -/G | 1.65537e-05 | 0.0028769 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716758 | TCTTTATACTGAACA[-/G]CTATAGGTTTAGAGA | 1130 |
rs749936152 | snp | C/T | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810390 | TTACGCTGTCGTCTG[C/T]TTTTTCGAAAAACAT | 1130 |
rs749945320 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235679985 | TCAATGCTTTTAAGG[-/CT]CTCTCTCTCTCTCTC | 1130 |
rs749965806 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235722335 | TGATCCAACATACTT[C/T]AGCTGCTGTGTTGAG | 1130 |
rs749967768 | snp | C/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731158 | AGGTTGGATAGTAGA[C/T]GGGGTCATACCATAC | 1130 |
rs749987595 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant | LYST | GRCh38.p7 | 1:235762885 | TTGAAACAGCAAAAT[C/T]TTTAAAAAGGATAAA | 1130 |
rs749990074 | snp | A/G | 1.66217e-05 | 0.0028828 | intron-variant | LYST | GRCh38.p7 | 1:235757497 | TTACTAACATGACAA[A/G]AAAAGTACTTGATGA | 1130 |
rs749998169 | snp | G/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762571 | GCCTCATCCATTTTC[G/T]CAATGCTCTTGAGGA | 1130 |
rs750005579 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235824198 | GTTCATAAATGTACA[A/G]CCCTCTTTGGTAAAA | 1130 |
rs750009496 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705850 | AGGCTGGAGTGCAGT[G/T]GCATGATCTTGGCTC | 1130 |
rs750015716 | snp | C/T | 1.65688e-05 | 0.00287821 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744120 | TTGAGTTACATTTTC[C/T]GGAGTTCTCAAAATG | 1130 |
rs750034738 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | LYST | GRCh38.p7 | 1:235720617 | ATAAAGAAATACAAC[A/G]TATGGATGGATGAAC | 1130 |
rs750051504 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707013 | TAGATTTGCTACAGT[C/T]GACACAGAAAATTAC | 1130 |
rs750083768 | snp | G/T | 1.6661e-05 | 0.00288621 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810498 | GAGTTCTTTTCTTTG[G/T]TCAGGATTATATCTG | 1130 |
rs750096710 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | LYST | GRCh38.p7 | 1:235663978 | AAGAGGGGGAGAAGA[C/T]CTTACCTGATGATGG | 1130 |
rs750096921 | snp | A/T | 1.66358e-05 | 0.00288402 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800925 | AATAATTTTCAAAAA[A/T]CTCTCAAATACATGG | 1130 |
rs750108334 | snp | A/C/G | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787211 | CTACCTCTGTCCAGA[A/C/G]ACCCATATGGAGATT | 1130 |
rs750118993 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235857140 | TTAGTAGAGATGGGG[C/T]TTCACCATGTTGGCC | 1130 |
rs750126016 | snp | A/C/T | 3.3004e-05 | 0.00406216 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757417 | CCACTTAGGAGTTCA[A/C/T]ATAATCCACAGCATA | 1130 |
rs750132268 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809210 | AACATCTCCATCTGC[A/G]GTCTCTTCAAATGGG | 1130 |
rs750136780 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant | LYST | GRCh38.p7 | 1:235804453 | GTCATCCCACACTTC[C/T]GCCTCTGCTGGTCAT | 1130 |
rs750164157 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235804255 | CTCGAAGTAATTCTC[A/C]GTAAATTTCCAGATT | 1130 |
rs750165771 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838147 | GGTGCTTCTATTTTC[G/T]TGGTGCAATAAACAG | 1130 |
rs750182942 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841201 | CTCCATCTCATGGTT[C/T]CCAATACCAGACCGA | 1130 |
rs750183373 | snp | A/G | 9.24924e-05 | 0.00679983 | intron-variant | LYST | GRCh38.p7 | 1:235791604 | TGAAGAACATGTTAA[A/G]AGTGTTAAGAACACT | 1130 |
rs750184895 | snp | C/G | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809223 | GCAGTCTCTTCAAAT[C/G]GGTTTTTGGAAACCT | 1130 |
rs750206977 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235869820 | TGGCTCCTCAAAACT[C/T]CGTCTCTTTCTACTC | 1130 |
rs750216031 | snp | C/T | 1.67142e-05 | 0.00289081 | intron-variant | LYST | GRCh38.p7 | 1:235709053 | ATATTCAGGTTCTAT[C/T]TTATATAAATACAGA | 1130 |
rs750232456 | snp | C/T | 1.6498e-05 | 0.00287206 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724130 | GTGAACTTCTTTAAT[C/T]TCTTCATATGTCCAG | 1130 |
rs750242808 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789047 | AGGGATGAAAAATGG[C/T]AATTCAGTACTTTAA | 1130 |
rs750251694 | snp | A/T | 1.65143e-05 | 0.00287348 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809675 | CTGAACCTCCTGCAG[A/T]GTTTTCTTTTGTCTT | 1130 |
rs750253633 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823763 | CCTGCCTCTTTACAT[C/T]GCCAATTCCTACTTA | 1130 |
rs750259072 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | LYST | GRCh38.p7 | 1:235662954 | TTCACCCGGCTGCAT[A/G]GCTGCTAAGGAAGGA | 1130 |
rs750259814 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682632 | AGTTAAAACCATAGA[A/G]ATGTAGTCGGATGAA | 1130 |
rs750262198 | in-del | -/GT | | | intron-variant | LYST | GRCh38.p7 | 1:235765373 | GCCTTACTGCCCCTA[-/GT]TCCTTATTCCTGAAT | 1130 |
rs750267847 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235665046 | TGATCAGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 1130 |
rs750285227 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759220 | GTCATCTTCTGACCT[A/G]GGTTCTGCTCCCAAC | 1130 |
rs750285805 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790983 | GAGAAACCGCTGTCT[C/G]TACTAAAAATACAAA | 1130 |
rs750307340 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838622 | TTTTAGAACATTATT[C/T]CTCCACAGGCTTCTA | 1130 |
rs750309788 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235882388 | TCCTGTGTGCCATGC[A/G]GAAGCTTTGGACTTT | 1130 |
rs750317952 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235731473 | CTACTATGAACACTT[C/T]AGCAACATAATACAA | 1130 |
rs750321102 | in-del | -/C | 0.000297422 | 0.0121911 | intron-variant | LYST | GRCh38.p7 | 1:235728181 | TGTATGTGCACACTA[-/C]CATTCATGGTTTAAT | 1130 |
rs750327931 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235714273 | TGGGATAGGACCATG[C/T]ATCCAGGAGGCCCTC | 1130 |
rs750331195 | snp | G/T | 4.94564e-05 | 0.0049725 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791755 | TTTCTTTTCTTTATC[G/T]TCTTTCCTTTTTCTG | 1130 |
rs750338502 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770249 | GCTGGTGGTGATCTG[C/T]TCTGATGAGGACTTC | 1130 |
rs750345692 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777192 | GCTCTGAACTTCTTT[C/T]GAGCTGAAGGGTCTT | 1130 |
rs750349681 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684449 | AGCAGGGTTTAGAAT[C/T]GATTTGTAGGGGAAG | 1130 |
rs750352917 | snp | A/G | 1.66244e-05 | 0.00288304 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808673 | CTGGATTAAATTGCA[A/G]ATGTGATTTGCAATC | 1130 |
rs750359481 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881137 | CAGGTCATAACGAAG[C/T]GGTAACTACAAAACT | 1130 |
rs750363224 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670960 | TATGATTCCCTCTGA[C/T]AACCCTCTAAGTCTC | 1130 |
rs750363631 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | LYST | GRCh38.p7 | 1:235709182 | TGACAGATGTTCTGC[A/G]ACACGTAGTCAGACT | 1130 |
rs750364103 | snp | C/G | 1.66768e-05 | 0.00288758 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777080 | TGGCAAAGAGAAAAA[C/G]AAATATGCCAGTTCC | 1130 |
rs750380385 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797186 | ACAGCAGCATTATAC[A/G]TAGTAGCAAAAAAGG | 1130 |
rs750398465 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808544 | GCTACATACATGACT[C/T]TGAGCTGAAGTAACG | 1130 |
rs750400335 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235812379 | TGGCATGGTGGTGCA[C/T]GACTGTAATCCCATC | 1130 |
rs750404448 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672193 | GTTAAGTTGAAAATG[C/T]TGTGTAGGCAATTAG | 1130 |
rs750413394 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235755724 | TCAGTGTAACACAAC[A/T]GTATTTGTAAATTAA | 1130 |
rs750413949 | snp | C/T | 1.78074e-05 | 0.00298385 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753052 | AACTTACTTCTTTTC[C/T]AATCCATTCAGGGCT | 1130 |
rs750417950 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235715702 | ATGAGAGGTGCTTCT[C/G]TCACTAGAGATGTCT | 1130 |
rs750431413 | snp | C/T | 4.97888e-05 | 0.00498918 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809897 | AGAAACTACTCGACT[C/T]TCCAAGTTGTCGCTC | 1130 |
rs750449601 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701949 | TACAAGGAATAATAG[C/T]CAAAACAAGGTGTAG | 1130 |
rs750450275 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857544 | AAGAGAAATGAGGAG[A/G]AGGAGAGAATCCAGA | 1130 |
rs750462786 | snp | A/C | 6.59663e-05 | 0.00574272 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806309 | TCTCGAGAGATATAC[A/C]TGGCAGCATATGACT | 1130 |
rs750469214 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862159 | AAACAGGCCAGTTGA[C/T]ATGATATGATATGAC | 1130 |
rs750470223 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | LYST | GRCh38.p7 | 1:235733819 | TGCCTTTGGAACATA[C/T]AAAATCTTACCTTTG | 1130 |
rs750493937 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810234 | TGGTCTTGTTTAGGA[A/G]ACGATGTTAAAAAAT | 1130 |
rs750498413 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738829 | CAATTTCCACCATGA[C/T]TGGTGGAATAAAGGA | 1130 |
rs750509278 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235783587 | AAACCACCATGGCAC[A/G]TGTATACCTATGTAA | 1130 |
rs750522125 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | LYST | GRCh38.p7 | 1:235693456 | AGGATGGCTGACCAC[C/T]GAATGTCCGTACTGT | 1130 |
rs750538801 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235689536 | GGTCAAAGGGTACAG[C/G]TTTCAGTTGTGCAGG | 1130 |
rs750548491 | snp | A/G | 4.95405e-05 | 0.00497673 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715339 | CTCTGGCTCCTTTGC[A/G]GTACTCTTCCTCCAA | 1130 |
rs750557044 | snp | C/T | 3.3012e-05 | 0.00406262 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809028 | GGCAATTTAAAAGCA[C/T]GGAGCAAAGGAATGA | 1130 |
rs750558084 | snp | C/T | 3.31488e-05 | 0.00407103 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746471 | GCTCATCATTTGCCA[C/T]TGAACGCATTTTCAT | 1130 |
rs750559217 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704152 | TTCTTTATCCAATCT[A/G]TCATTGATAGCCATT | 1130 |
rs750588433 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740249 | ATCCTTTTTAATATA[C/T]CCTCTCTCATCTCTA | 1130 |
rs750594568 | snp | A/T | 1.65029e-05 | 0.00287248 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734436 | GTCAATCATTCTTTA[A/T]CTATGATGGAATCTC | 1130 |
rs750610685 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736171 | ATTTCAGGGACTATA[A/G]AAGGTGTCACTGGGA | 1130 |
rs750618554 | snp | C/T | 6.60382e-05 | 0.00574585 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770282 | GAGCTGCTAGCAAAG[C/T]TTCCCAAACACCTTG | 1130 |
rs750626080 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235799140 | ACTAAATAAGTAAAT[C/G]AATGAGAAGAGAAAG | 1130 |
rs750660081 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702170 | GAATTGAGTTGAAGA[-/T]TAAAATCCACTTTAG | 1130 |
rs750661596 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676165 | TGATATATTTTTGTC[A/T]TGTAATTTTTAAGGC | 1130 |
rs750662250 | snp | C/T | 1.65222e-05 | 0.00287417 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235782021 | AATCATGCAAAATGT[C/T]TTATTGCTATCAGAT | 1130 |
rs750673749 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235741719 | AAAGAAGATTATGGA[A/T]CACGTTTTATTCCAG | 1130 |
rs750674384 | in-del | -/AAC | | | intron-variant | LYST | GRCh38.p7 | 1:235776289 | ATTTGTAAGAACCCT[-/AAC]AACAACAAACGCTGA | 1130 |
rs750683110 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235803588 | AGAGTTCCAGTACTA[A/C]CTTCCTGTGTAAGAA | 1130 |
rs750690676 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235724437 | ATACAGAATTCTCAC[A/G]TATCCTCCCCTCCCT | 1130 |
rs750716679 | snp | A/G | 1.6571e-05 | 0.0028784 | missense | LYST | GRCh38.p7 | 1:235664573 | CAGTGGACATGTCCA[A/G]CGAGATCCCCGTTCA | 1130 |
rs750717184 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840967 | GGTTAACTGGATAAA[C/T]GGTACTGTCACCTGC | 1130 |
rs750720378 | snp | A/T | 1.70653e-05 | 0.00292102 | intron-variant | LYST | GRCh38.p7 | 1:235697051 | CTCACGAAAGATATA[A/T]CCAGAATGATCTTCG | 1130 |
rs750729884 | snp | C/T | 6.60884e-05 | 0.00574803 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730851 | TTCAAAGTTACCTTA[C/T]AGATTCACTTGCAGC | 1130 |
rs750730548 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235783000 | AAAAGGCAAAATAAG[A/G]CTTTCTCACAGAAAG | 1130 |
rs750732627 | snp | C/T | 6.60229e-05 | 0.00574518 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806387 | CATTGGCCGACTCCC[C/T]GTCAGACTCTGCTTC | 1130 |
rs750735582 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819515 | TGAGGTGTTCCCTCA[C/T]GACATCCAAGTGGGA | 1130 |
rs750747229 | snp | A/G | 3.34504e-05 | 0.00408951 | intron-variant | LYST | GRCh38.p7 | 1:235805722 | TATTACATAAGAGTT[A/G]GACTAAGGACAAGGT | 1130 |
rs750760497 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235839253 | TGTATGTGTGCATAT[A/G]TATATATACAGTTTT | 1130 |
rs750766090 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695870 | TCGATCTCCTGACTT[C/T]GTGATCTGCCCGCCT | 1130 |
rs750768509 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708860 | GAATCCTCAAGTCCA[C/T]CTAGTGAATCATCAA | 1130 |
rs750772924 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702853 | TTGAGCTTGGCTCCA[A/G]GTCTGCTCACATGGG | 1130 |
rs750778817 | snp | C/G | 3.30934e-05 | 0.00406763 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741538 | ACAAAATATGCACTA[C/G]TAGTCTCCCAAGCTG | 1130 |
rs750783161 | snp | A/T | 1.89755e-05 | 0.00308016 | intron-variant | LYST | GRCh38.p7 | 1:235830427 | GCTCATGACCGAGCT[A/T]TAAAATAAGTATTAC | 1130 |
rs750794054 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733687 | AATCCAGACGCTGAA[A/G]GAGACTAAACAAATA | 1130 |
rs750799031 | in-del | -/ATCTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235755998 | ATGCTCTCTCTGCAA[-/ATCTAT]ATCTATATCTATATC | 1130 |
rs750804718 | snp | A/G | 1.67789e-05 | 0.00289641 | intron-variant | LYST | GRCh38.p7 | 1:235664438 | TTATGAATGAAATCA[A/G]AAAAAGAGAATCCAA | 1130 |
rs750810868 | snp | G/T | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806330 | GCATATGACTTAAAG[G/T]CTCGCTGGCTGTGCT | 1130 |
rs750811768 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710142 | ATTAAGTTGCTGTCT[A/G]TCTACTTTTTGATCT | 1130 |
rs750822794 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235766444 | AATTGAGTTATTTCC[C/T]AATTCAAGCAATCTT | 1130 |
rs750835647 | in-del | -/A | 1.64985e-05 | 0.0028721 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805942 | ATATGCTGTAACTCT[-/A]ATTTACCTAAACTGT | 1130 |
rs750848002 | in-del | -/TTTTA | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868698 | TACCAGTGTTTTTTA[-/TTTTA]TTTTATTTTATTTTC | 1130 |
rs750855610 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753809 | TCTCAAGGCTATTGT[G/T]AGAATCAAATAAAGT | 1130 |
rs750856402 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235800446 | AAGCATGAAACAACT[A/G]CAATGTCATAATAAA | 1130 |
rs750867387 | snp | C/T | 1.66557e-05 | 0.00288575 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775006 | TAATTCATGTACTCT[C/T]TGTTGGTTGTATTTA | 1130 |
rs750867508 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235870333 | GTGTCAATCCCTGAG[-/T]TTTTGGCCAATCAAA | 1130 |
rs750886970 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755547 | AATTCTTGAGTTCCT[C/T]GATGAAGATACAACT | 1130 |
rs750889175 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700436 | GATATGAACAGCCAC[-/T]TTCTCATAGAATATT | 1130 |
rs750892804 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235723172 | TGTCATTTACTGAGA[C/T]AGAGAAAACTGGAAG | 1130 |
rs750898732 | snp | G/T | 3.5966e-05 | 0.00424049 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792119 | GAATACCCAGAAGAA[G/T]AATTTTCTAGAGAAA | 1130 |
rs750905004 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807293 | GAATTTCCCTTCTAA[C/T]TGGGCTAATTGAACA | 1130 |
rs750905230 | snp | G/T | 4.94915e-05 | 0.00497426 | intron-variant | LYST | GRCh38.p7 | 1:235731008 | CTGCTATATTTATAT[G/T]TTGAGTCAAGAAGCC | 1130 |
rs750916490 | snp | A/C/T | 3.30563e-05 | 0.00406538 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715196 | GGCAGTTATTAAATT[A/C/T]TTACCTTGATAGGCT | 1130 |
rs750935624 | snp | G/T | 3.40507e-05 | 0.00412604 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781006 | TACAGATGTATGGTT[G/T]GGTCCACAAGCATAC | 1130 |
rs750941523 | snp | A/G | 0.000329728 | 0.0128357 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792021 | TTGTGATGAAACACC[A/G]TTGCTTAAATTTGGA | 1130 |
rs750945242 | in-del | -/AG | 2.01371e-05 | 0.00317304 | intron-variant | LYST | GRCh38.p7 | 1:235793461 | AAAATTGTAAGTGAA[-/AG]AATTTATCAGTGAAA | 1130 |
rs750974811 | snp | A/C | 1.90445e-05 | 0.00308576 | intron-variant | LYST | GRCh38.p7 | 1:235759642 | CTTAAAAATCTATTA[A/C]GTGGAACCACCTCTC | 1130 |
rs750980551 | snp | A/G | 8.24069e-05 | 0.00641846 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810172 | AAGCCATAGCATCTG[A/G]AGGAGTCTGTTCTTT | 1130 |
rs750986055 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805877 | TAAATAGCTTTGCTT[C/T]CTCGGGAGCGGCTTC | 1130 |
rs751038938 | snp | A/G | 1.6519e-05 | 0.00287388 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800953 | TGGGCAAGCACATCA[A/G]GTTTGGCTTTACTAG | 1130 |
rs751039302 | snp | A/T | 1.6504e-05 | 0.00287258 | intron-variant | LYST | GRCh38.p7 | 1:235720628 | CAACATATGGATGGA[A/T]GAACCCTAAAGGTGA | 1130 |
rs751046549 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868671 | TGCCATTTGTGACTA[C/T]TATTTTTTTCGGTAC | 1130 |
rs751066526 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235685704 | TACAAAAATTAGCCG[A/G]GTGTGGTGGTGTGCG | 1130 |
rs751067321 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235736138 | ATTTTAATACCCTCT[G/T]ATCACTTACTGATGA | 1130 |
rs751069242 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235879120 | AAGCAATCCTCCCAC[C/T]TCAGCCTCCCAAAGC | 1130 |
rs751071469 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720763 | TTGAAGGATCGGCCA[C/G]CATGTTTGTTTAAGT | 1130 |
rs751093991 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235774505 | AGCACGAATATCTGT[A/G]ACTTGAAAAACTAAC | 1130 |
rs751111866 | snp | C/T | 3.33467e-05 | 0.00408316 | intron-variant | LYST | GRCh38.p7 | 1:235757507 | GACAAGAAAAGTACT[C/T]GATGATTACCTTAGG | 1130 |
rs751121624 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733629 | GAGAGAGACACTGCC[C/T]GGGTGATATCTGCAG | 1130 |
rs751122488 | snp | C/T | 1.76508e-05 | 0.00297071 | intron-variant | LYST | GRCh38.p7 | 1:235766316 | TTTAGATTTAAAGAA[C/T]TGTCAACTTAACTAA | 1130 |
rs751124526 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673433 | TATGGTGGGGAGATC[A/G]GCACTCTCTCCCCAA | 1130 |
rs751133295 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235776420 | GGGATAAAACGAAGA[C/T]GGCATTCCGAGGATG | 1130 |
rs751146658 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718824 | CAAAGTAAGGAATTG[A/G]TGCCCTATTACCTCT | 1130 |
rs751151484 | snp | C/T | 1.79133e-05 | 0.00299271 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806768 | AAAACAAATCTCTTA[C/T]TACCCTGTGAAAGAA | 1130 |
rs751161625 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674014 | AGAATATGAACTGCA[C/T]AGCAGCTCTCTTCCA | 1130 |
rs751165344 | snp | C/T | 2.44879e-05 | 0.00349905 | intron-variant | LYST | GRCh38.p7 | 1:235734696 | TTTAGTCATTTAGAA[C/T]TTTAATTCTTACATT | 1130 |
rs751173124 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845714 | GGCTCCGACTGCTGG[C/T]TTTCCCCCACTTCCC | 1130 |
rs751192896 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878083 | TTTAAACATGTCTGG[A/G]CCCACTTAATAATGT | 1130 |
rs751211933 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235851190 | GTATATGTGTGTGTA[-/TA]TATATATATATATGA | 1130 |
rs751219281 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235760841 | GCTAGAGGGCTAAAG[C/T]TGCCAAAAGATTCTC | 1130 |
rs751221097 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859319 | TCCCTTTCCCTCAAT[C/T]CACTGAAGTGTCCTT | 1130 |
rs751234673 | snp | C/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759012 | AATTTGGCTCATAAC[C/G]AAGAGAATAGGCAAA | 1130 |
rs751236237 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235720348 | GATATCATGGAATTA[C/T]TGTCAATTTTCTTAC | 1130 |
rs751239599 | snp | C/T | 4.95307e-05 | 0.00497623 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809437 | AGGCCTCGGGAGGAA[C/T]TCCATCTCTTAAAAC | 1130 |
rs751243581 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661832 | TATGGGAGAGACAGA[C/T]GGCTCCAAGATGTTT | 1130 |
rs751270631 | snp | C/T | 3.6205e-05 | 0.00425455 | intron-variant | LYST | GRCh38.p7 | 1:235788670 | ATTTAAATACATTAT[C/T]TATTCATGGGAGGCT | 1130 |
rs751277783 | in-del | -/ATTAAATTAT | 4.58285e-05 | 0.00478666 | intron-variant | LYST | GRCh38.p7 | 1:235734729 | AATTACTTAGTAGTA[-/ATTAAATTAT]ATTGCTAGATTTATT | 1130 |
rs751289194 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235829184 | CTCCAGCCTGGGCGA[A/C]AGAGCGAGACTCTGT | 1130 |
rs751291435 | snp | G/T | 1.66432e-05 | 0.00288467 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808698 | GCAATCTGTATACTA[G/T]GTAATCTGTCTTCTT | 1130 |
rs751294097 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806662 | TGCTCCCCTAGGCTG[A/G]TTATCAGAGTTTCAA | 1130 |
rs751320821 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777201 | TTCTTTTGAGCTGAA[A/G]GGTCTTTGAGAGAGT | 1130 |
rs751325983 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817099 | AGAAGACATACATGC[A/G]CCAACAAGCATATGA | 1130 |
rs751332619 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705703 | GTGATACTTTTAATG[C/T]AAATTTTATATAAGA | 1130 |
rs751365713 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235858320 | ATATGTGAAACATAA[C/G]CATGATAACCTATGG | 1130 |
rs751369611 | snp | G/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762287 | CTTGAAAGCATTCTT[G/T]ATGATGATAAAGTCC | 1130 |
rs751371601 | snp | C/T | 1.65135e-05 | 0.00287341 | missense | LYST | GRCh38.p7 | 1:235709209 | GACTCTAGAGCCTGC[C/T]GATGGATGAGGATAA | 1130 |
rs751381504 | snp | A/G | 3.32149e-05 | 0.00407509 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809909 | ACTCTCCAAGTTGTC[A/G]CTCAGACTGCAGCAG | 1130 |
rs751412811 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235836830 | GTGAGGGAAAATAAC[A/G]TTCAGTTTTAGCTAT | 1130 |
rs751429062 | snp | G/T | 3.30175e-05 | 0.00406296 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753171 | GTAAAAGAGCATTAT[G/T]CAAGAGTATGTTGTC | 1130 |
rs751435380 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235694337 | TTTTTTACAACATAG[C/T]ATGATGTTCTCTTGG | 1130 |
rs751439794 | snp | A/C | 6.62383e-05 | 0.00575454 | synonymous-codon, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766137 | GTAAGTATTAGTAGG[A/C]GGGTGAACTGCTAAA | 1130 |
rs751441733 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838072 | GAATGTCAGAGAATA[C/T]GAGTATAGATGTAGG | 1130 |
rs751457035 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235736771 | CTTTGCTATCTTTCT[C/T]TGTGTTATGAAGTAG | 1130 |
rs751460026 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235871511 | TTAAGACTAGGTTTT[G/T]CTTTAAAGATCATAT | 1130 |
rs751466428 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768736 | AATAAGAATATCACA[C/T]TGTCATATGAACTTA | 1130 |
rs751487441 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235728429 | TGTGCTCAGTGCTAA[A/G]TAAATGTTGGCTATT | 1130 |
rs751490458 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806196 | ACCAAGCCTATAAAA[C/T]TGTTTCTGGAACACT | 1130 |
rs751495524 | snp | C/T | 3.30524e-05 | 0.00406511 | intron-variant | LYST | GRCh38.p7 | 1:235746325 | AAAACAAACTAATCC[C/T]ATAGTCTTACCTTGA | 1130 |
rs751500858 | in-del | -/AAAAT | | | intron-variant | LYST | GRCh38.p7 | 1:235748465 | ATTTTGTAATCATTA[-/AAAAT]AAAAGAATATTTATG | 1130 |
rs751508354 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235733252 | CTATTCTTTTACAGA[C/T]CATATTTTAAAATTA | 1130 |
rs751509211 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235788565 | GGTATTAATAGCTGT[C/T]AGAATGTATATATTT | 1130 |
rs751511204 | snp | A/C/T | 0.000132099 | 0.0081261 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806106 | ATCTCCCTCCTTTTT[A/C/T]CCTTGCTCCTCTTTG | 1130 |
rs751525262 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681416 | TGCCTAGCAACCTAC[A/G]TTTTATCCCCGAAGC | 1130 |
rs751525949 | snp | C/T | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806500 | TTTGGATAAGCTTCT[C/T]TGAGGCCAGCATAAA | 1130 |
rs751557247 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769495 | AATATTACTGATCTC[A/G]TGGAGTATCTGTACT | 1130 |
rs751561627 | snp | A/T | 1.66062e-05 | 0.00288146 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808854 | TCACATAAGTTTCCC[A/T]GCAGTGTCTCTTCTA | 1130 |
rs751575435 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235723611 | CATTACGGGTTTAGC[A/C]ACATAGAGGTTACCG | 1130 |
rs751579972 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235729782 | TTCCAATAGCATGAG[G/T]TATCTTGTCGAAACC | 1130 |
rs751581438 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830268 | AAGTAATAGAAATCC[C/T]CGACCATGGACAAGG | 1130 |
rs751597672 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753386 | AGTCATAAAAACAAG[A/T]TGGGGGAGTAAGGAT | 1130 |
rs751609899 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809181 | GCAATGCAACAGCAC[C/T]GCTCAGGATAATAAA | 1130 |
rs751616829 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235666714 | AGATGCAGGAGACTC[A/T]GTATGCTAAAGAAAT | 1130 |
rs751627465 | in-del | -/AC | 1.65053e-05 | 0.0028727 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806470 | TGAACATCTTGGTTA[-/AC]AGTCTTCCGTCTCTT | 1130 |
rs751643983 | in-del | -/A | 1.66799e-05 | 0.00288785 | intron-variant | LYST | GRCh38.p7 | 1:235793631 | ATTAAAGAAAGAGGG[-/A]AAAAAATTAAAGCTA | 1130 |
rs751658977 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751202 | TAAAATATGATTTCA[A/G]TACTCGCCAGCAATG | 1130 |
rs751669600 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235882733 | GGGCTAGCAGTGAGG[A/C]GTGAGAAGGAGAGAA | 1130 |
rs751683609 | snp | A/G | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885420 | ATCAAGTTTATTACT[A/G]TCCTTAGAAATTGAT | 1130 |
rs751688667 | snp | A/G | 4.97558e-05 | 0.00498753 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773856 | CCTCTGCTTTACTCC[A/G]TATCTTCCAGTCAAG | 1130 |
rs751710590 | snp | C/T | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806394 | CGACTCCCTGTCAGA[C/T]TCTGCTTCTTTACTT | 1130 |
rs751710591 | snp | A/G | 1.65921e-05 | 0.00288024 | intron-variant | LYST | GRCh38.p7 | 1:235697071 | AATGATCTTCGTTAC[A/G]TTTTATTTTACCTTG | 1130 |
rs751730165 | snp | A/G | 1.65053e-05 | 0.0028727 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734441 | TCATTCTTTATCTAT[A/G]ATGGAATCTCCTAAG | 1130 |
rs751733054 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235787483 | GATTAAAAATCAGTT[C/G]TATTTTTTTTAAAGT | 1130 |
rs751733793 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235863419 | TAGTAAAAGGCGAAA[G/T]ATTTATACAATTTGA | 1130 |
rs751738472 | in-del | -/AG | | | intron-variant | LYST | GRCh38.p7 | 1:235674168 | TGTGTCTCTCACGAC[-/AG]GGGGAATATTTGGCA | 1130 |
rs751741419 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670809 | GGGGGGTTAAGTCTC[C/T]AGGGAAAGGGTGCAA | 1130 |
rs751744087 | snp | A/T | 3.2993e-05 | 0.00406145 | intron-variant | LYST | GRCh38.p7 | 1:235728056 | GATTTATGTAAATAC[A/T]GACTTAAGCCTCTAC | 1130 |
rs751756619 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235849351 | TCAGCAAAATCGGCA[A/T]ACAAGGGTCATACCT | 1130 |
rs751798406 | snp | C/T | 3.29636e-05 | 0.00405964 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804551 | CTGCTGAATAATTCC[C/T]GAGGGCAACTCGAAG | 1130 |
rs751813278 | snp | G/T | 1.65318e-05 | 0.002875 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773965 | CATATAAATAATATC[G/T]TCACCACAGCATCCT | 1130 |
rs751818373 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235694636 | TTTTGCTGAGTAAAA[-/T]AAGAAATGTTGACAA | 1130 |
rs751832714 | snp | A/C/T | 4.23812e-05 | 0.00460317 | intron-variant | LYST | GRCh38.p7 | 1:235792147 | AAAAAGAAAAACAAA[A/C/T]GAAACTTTCTAATCA | 1130 |
rs751848442 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235801386 | CATGGACACAACTTT[-/A]AAAAAAAAAAACCTA | 1130 |
rs751850677 | snp | C/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738814 | TTAGGCGGGTGCACC[C/G]AATTTCCACCATGAT | 1130 |
rs751859873 | snp | A/G | 5.01777e-05 | 0.00500863 | intron-variant | LYST | GRCh38.p7 | 1:235715372 | ACTGAAAGAAACGGT[A/G]AATCCAGAGAATTCA | 1130 |
rs751860031 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740119 | AAAAGGAAGACAGTG[C/T]CCTCAGTGTACTTGA | 1130 |
rs751864744 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831996 | ACAATATCACCTTCT[A/G]GGCCATCAAGACCAT | 1130 |
rs751870447 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689252 | CTTTATTTTCATCTA[C/T]TATGATACAAATAAT | 1130 |
rs751871167 | snp | A/C | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830328 | CTCCTCTTCTTCCTC[A/C]CTGGCCTCCACCCTC | 1130 |
rs751878407 | snp | A/C | 0.000197954 | 0.00994676 | intron-variant | LYST | GRCh38.p7 | 1:235731015 | ATTTATATGTTGAGT[A/C]AAGAAGCCACTATTA | 1130 |
rs751887786 | snp | A/G | 0.000209911 | 0.0102426 | intron-variant | LYST | GRCh38.p7 | 1:235663127 | ATATTTCTTAAAAGT[A/G]TATTAGCATATTGGT | 1130 |
rs751887788 | snp | A/C | 1.64844e-05 | 0.00287087 | intron-variant | LYST | GRCh38.p7 | 1:235804461 | ACACTTCCGCCTCTG[A/C]TGGTCATACCCAAAG | 1130 |
rs751888192 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235797465 | CCTCTCAAAAGTCCA[C/T]ACCCCTAGCATAATC | 1130 |
rs751892711 | snp | A/G | 9.90393e-05 | 0.00703632 | intron-variant | LYST | GRCh38.p7 | 1:235677042 | CCACTGGCCGAATGC[A/G]CTGTTAGAGCACCAG | 1130 |
rs751904873 | snp | G/T | 1.64806e-05 | 0.00287054 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810183 | TCTGGAGGAGTCTGT[G/T]CTTTGGTTGCTAAGC | 1130 |
rs751911743 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875973 | GCTTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 1130 |
rs751915380 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235668075 | ATAAGAAAAAAGTCT[-/G]TACATACTAAGTACA | 1130 |
rs751940651 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731145 | TCCAACTGCCATGAG[A/G]TTGGATAGTAGATGG | 1130 |
rs751942690 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235722757 | CCAAAATGCTGGGAT[C/T]ACAGGCATGAGCCAC | 1130 |
rs751947602 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724117 | GCCACCAACGCTTGT[A/G]AACTTCTTTAATTTC | 1130 |
rs751952509 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818533 | CATGTGCTTTACTTC[C/T]AAATAATAAAACTAA | 1130 |
rs752000050 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771950 | TTTTTGGCCAGGCAT[-/G]GGGGGGCTCACGCCT | 1130 |
rs752001217 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874608 | GTAATGCAGAAAACA[C/T]TTTTTTCATAAAGCT | 1130 |
rs752010313 | snp | A/G | 9.93739e-05 | 0.0070482 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762772 | TACCATAAATCCAGG[A/G]CTCATAAGGGACCTT | 1130 |
rs752039194 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874134 | GGTGCTACATAAAAA[G/T]ATTCTGAATATTTAC | 1130 |
rs752040613 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235819267 | TCCTCTGGGTGCATT[A/C]CTTTTTTATTAATAT | 1130 |
rs752048221 | snp | A/T | 2.72387e-05 | 0.00369034 | intron-variant | LYST | GRCh38.p7 | 1:235746552 | TATATAAATTAAAAC[A/T]TCAAATCCCAGTGTT | 1130 |
rs752051681 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235707344 | TATACTTGAAAATGT[A/T]GGCCAGACATGGTGG | 1130 |
rs752056490 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697919 | AACAATAGGATTTGG[A/G]GGAAGAAAGGTGAGT | 1130 |
rs752072103 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235841415 | GGCCAGCCATCTCCT[A/G]TCAGCTCTGATTGTG | 1130 |
rs752075448 | snp | C/T | 3.32823e-05 | 0.00407922 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781930 | TAGCTCACTCACCGT[C/T]GAAGAGAAGCAAATT | 1130 |
rs752098107 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746873 | ACTGTTTCACTTCTT[C/T]GTATTCCAAAATCAA | 1130 |
rs752109881 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235726419 | AATTCTTCCTTTGTT[C/T]AGTTTCAACATTCAT | 1130 |
rs752123968 | snp | C/T | 6.61037e-05 | 0.00574869 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793566 | TTCTGAACATGTTCT[C/T]GAACTCATCAAAGAT | 1130 |
rs752133510 | snp | C/T | 0.000106352 | 0.00729143 | intron-variant | LYST | GRCh38.p7 | 1:235755696 | CATTAAAATTAAATA[C/T]AATATATACAAATCA | 1130 |
rs752141246 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708642 | TCTTGCACACTGAGC[C/T]TCTAATGAGATTCCC | 1130 |
rs752144069 | in-del | -/AAGT | | | intron-variant | LYST | GRCh38.p7 | 1:235771339 | ATTTCAAATCCATAG[-/AAGT]AATATGTGTCTTATC | 1130 |
rs752160342 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702780 | GACCTGTTCTCGGGT[C/T]TCCCTGAAAGCAAAC | 1130 |
rs752162504 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807242 | GGGAAAGAATCACAC[G/T]AGAGCTGAAAATCTA | 1130 |
rs752173624 | snp | C/T | 6.62877e-05 | 0.00575669 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741415 | TTATCAAAGCTGAGA[C/T]ACTTACTTGTAGGGA | 1130 |
rs752173793 | snp | A/G | 1.66868e-05 | 0.00288845 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752091 | TATTGTGAGCCTGAG[A/G]AACTGCAAGCATGAA | 1130 |
rs752179440 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806191 | AAACCACCAAGCCTA[C/T]AAAACTGTTTCTGGA | 1130 |
rs752192687 | snp | A/G | 6.60426e-05 | 0.00574604 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809635 | GAAGGGCTCTATGAC[A/G]ATACTTTGAAAACAC | 1130 |
rs752194808 | snp | A/C | 2.04836e-05 | 0.00320022 | intron-variant | LYST | GRCh38.p7 | 1:235806787 | CCTGTGAAAGAAAAA[A/C]AGCATGTAAAAAGGT | 1130 |
rs752200393 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235747637 | TCCTAATGTCTACAT[A/C]TGACAGCTTTCATGC | 1130 |
rs752233189 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697826 | ATATTGCGAGGATTA[C/G]AGAATCTCTAGCCAG | 1130 |
rs752236001 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867222 | CCTCCTCCCAGGGCT[C/T]TGCGTAGTGGGCTGC | 1130 |
rs752244699 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868613 | GATAATGGTATACAA[C/T]TGGCCCTCAAAGTAT | 1130 |
rs752246731 | snp | C/G | 4.94197e-05 | 0.00497066 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702873 | GCTCACATGGGCCAT[C/G]TGGAACAGCTGACGG | 1130 |
rs752252040 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853704 | GAAACCTGGGGCGCT[A/G]ACCTAGGGAGGAGAG | 1130 |
rs752256025 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235691349 | GAGATTAAGTTACTA[-/G]TCAAAGGCTGCAGTT | 1130 |
rs752263463 | snp | A/C | 1.85386e-05 | 0.0030445 | intron-variant | LYST | GRCh38.p7 | 1:235751991 | TCCCCAAATTCATAA[A/C]AATTAAATCTTACTT | 1130 |
rs752266951 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235791380 | TTTATCCTTTTATAA[C/T]ATCAGGAGCCACCCT | 1130 |
rs752268331 | snp | A/G | 1.6701e-05 | 0.00288968 | intron-variant | LYST | GRCh38.p7 | 1:235720936 | AAGAAAAAAACCCAG[A/G]TATTATTTTTAGTCT | 1130 |
rs752276719 | snp | A/G | 3.68229e-05 | 0.0042907 | intron-variant | LYST | GRCh38.p7 | 1:235777014 | TTTAATTTATCAATA[A/G]TAAGTAAGTCATTTC | 1130 |
rs752278969 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827269 | AGCTACTCAGGTGGC[C/T]GAGACATGACAACCT | 1130 |
rs752279597 | snp | A/G | 1.88799e-05 | 0.00307239 | intron-variant | LYST | GRCh38.p7 | 1:235813100 | TTCATGTTCTAAGGC[A/G]ATAAGACACATCAGT | 1130 |
rs752284421 | snp | C/T | 1.65247e-05 | 0.00287438 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809474 | TTCCATTTGAAGAAC[C/T]GCTGTTTCAAATAAA | 1130 |
rs752292065 | snp | A/C | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734407 | CAATGATAGCCTGTT[A/C]TTAAAAAAGTAGTGT | 1130 |
rs752296204 | snp | A/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868842 | CTGGGATTACAGGAA[A/T]GTGCTACCATGCCCG | 1130 |
rs752301488 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685611 | CAGCACTTTGGAGGC[C/T]GAGGCGGGTGGATCA | 1130 |
rs752318064 | snp | A/C | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759084 | AACGGCCAACAGCTG[A/C]AGATCCGTTCTGTGA | 1130 |
rs752327868 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717605 | GGCACAGGCATGGGA[C/T]CACCTGGATTTCAAC | 1130 |
rs752332721 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235880865 | GCACGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 1130 |
rs752348553 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847469 | GAACAAAAATGCAAG[A/T]TAAAAAGCAAAAACA | 1130 |
rs752356012 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772292 | TAAATTTTTAGGGAC[C/T]GTTGGCAAGTTGGGA | 1130 |
rs752361473 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235778099 | AGTTAACCCAGTTAA[-/AT]ATATATATATATATA | 1130 |
rs752369055 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813929 | GATTTGCTGAACAGA[A/T]TTAGTTGGAAGGGGA | 1130 |
rs752382223 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235736021 | GGTATTCAATGACAT[G/T]CAAAAATTATCTTGA | 1130 |
rs752386617 | snp | A/G | 1.68301e-05 | 0.00290082 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762675 | TATCTAAGAATATTC[A/G]GAACTAAAATGAGAA | 1130 |
rs752391476 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673226 | AGTCTGTCTCTTTTT[C/T]TTTCTCTTCTCTTTC | 1130 |
rs752401382 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703503 | ATCCCGTAGAGTCAG[A/G]TGGAGAGCAATGCAC | 1130 |
rs752402013 | snp | A/G | 1.66158e-05 | 0.0028823 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775028 | TTGTATTTAATTAAT[A/G]AGAGTATAACTCGCA | 1130 |
rs752406005 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672408 | AAGACTGAGAAGGAC[C/T]CACCAGTGACCTAGA | 1130 |
rs752446158 | in-del | -/A | 3.42059e-05 | 0.00413543 | intron-variant | LYST | GRCh38.p7 | 1:235766287 | TATTCCTGAAAAAAT[-/A]AAAAAAAACTCTCTT | 1130 |
rs752470030 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718706 | CATATTAAACGAACA[A/G]AATATTCCCTCATCA | 1130 |
rs752471768 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828973 | ACTTTGGGAGGCCAA[C/T]GGGGGTAGACTGCTT | 1130 |
rs752483569 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235784799 | CCAGCCCCAGCTCCA[C/T]CTGATTTAACTATAG | 1130 |
rs752510934 | snp | A/C/T | 4.99142e-05 | 0.0049955 | intron-variant | LYST | GRCh38.p7 | 1:235677652 | AGTATGAGATAAAAA[A/C/T]CACAACAAAAAGTAC | 1130 |
rs752516345 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710957 | ATGTGCTCCAGCTGC[C/G]TAAGGCTTCATCTCC | 1130 |
rs752518633 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235786948 | GATATACCTAATGTA[A/G]ATGACGAGTTAATGG | 1130 |
rs752527626 | in-del | -/AA | 1.65634e-05 | 0.00287775 | intron-variant | LYST | GRCh38.p7 | 1:235709076 | AATACAGATTGTTTT[-/AA]AAGAGTCACTTACAG | 1130 |
rs752559615 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814906 | CTCCGCATACATCTA[G/T]CTGGTAAAGGTTTCC | 1130 |
rs752586942 | snp | A/G | 1.72291e-05 | 0.002935 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780944 | AAAATTTCTTTATTA[A/G]TATATTTGGAGTAGT | 1130 |
rs752589897 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820496 | CGCCCCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 1130 |
rs752592323 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235704349 | TGCCTTCCACAGTGG[C/T]TGAACTAATTTACAT | 1130 |
rs752596657 | snp | A/C | 1.66037e-05 | 0.00288125 | intron-variant | LYST | GRCh38.p7 | 1:235801101 | TTAAGTCTACCCCTG[A/C]AAAGAGAAAAGCGAA | 1130 |
rs752603073 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235801189 | ATCTAGTGGCAAAAA[C/T]AGTAATTCAGAGGAT | 1130 |
rs752605708 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743403 | TTTAGATTTAGAGAT[C/T]GACATGTCATGATTT | 1130 |
rs752606040 | snp | C/T | 8.91274e-05 | 0.00667501 | intron-variant | LYST | GRCh38.p7 | 1:235766323 | TTAAAGAATTGTCAA[C/T]TTAACTAAGATTTTT | 1130 |
rs752611982 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817901 | TACCACAAAAATGAT[C/G]TATTCATTAAGAGTT | 1130 |
rs752615981 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858613 | ATTATCCACATTTAC[C/T]AGCCTTGTCTTGGCT | 1130 |
rs752621897 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235760565 | TCTGTGGACTGGTAG[C/T]ATGGGCATCAATACC | 1130 |
rs752622346 | snp | A/G | 3.70617e-05 | 0.00430459 | intron-variant | LYST | GRCh38.p7 | 1:235812960 | TGATATGATAAAGGG[A/G]AAAAGCATACCTGTT | 1130 |
rs752644083 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720808 | AAATTAGTAATTTGC[C/T]CAGTATACCATAAAT | 1130 |
rs752644520 | snp | A/G | 6.6084e-05 | 0.00574784 | intron-variant | LYST | GRCh38.p7 | 1:235733736 | AAGCATACATGGAAC[A/G]TATTTATCAGAACAT | 1130 |
rs752675762 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235835640 | ATGTGTCCTCCTTGA[A/G]TCTGCCAGCACTCTT | 1130 |
rs752682898 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693082 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATAAC | 1130 |
rs752686730 | snp | G/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806296 | GGCAAGACAAGGCTC[G/T]CGAGAGATATACATG | 1130 |
rs752690677 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802844 | GTGGTATTATTATGA[A/G]CCATTTTGCTATTTA | 1130 |
rs752708003 | snp | C/T | 1.65356e-05 | 0.00287533 | intron-variant | LYST | GRCh38.p7 | 1:235728181 | TGTATGTGCACACTA[C/T]CATTCATGGTTTAAT | 1130 |
rs752728695 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792666 | TGTTTCATGTTTAGA[-/T]TTTTTTTTTTTTTTG | 1130 |
rs752759775 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838208 | AAGGAGGTGTTAAAC[C/T]GATGAGTGTAACAGG | 1130 |
rs752805538 | snp | A/G | 1.65985e-05 | 0.00288079 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830392 | GTCAGAAATTCACGT[A/G]CCAGTGAGTTACTGT | 1130 |
rs752808092 | snp | A/G | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660687 | CATCCTGGCTAACAC[A/G]GTGAAGCCCCGTCTC | 1130 |
rs752812168 | in-del | -/GCCGCCACCCACACACATACAAACCTG | 3.36876e-05 | 0.00410398 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808430 | ACAACCCCCGCCCCC[-/GCCGCCACCCACACACATACAAACCTG]GCCGCCACCCACACA | 1130 |
rs752813977 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235871763 | TATACTCTGCAGCTC[G/T]CCCTGAATTCTTTCC | 1130 |
rs752830521 | snp | A/T | 1.95532e-05 | 0.0031267 | intron-variant | LYST | GRCh38.p7 | 1:235734683 | AAAGTAATAATTTTT[A/T]AGTCATTTAGAATTT | 1130 |
rs752845472 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | LYST | GRCh38.p7 | 1:235663952 | CAATCACAAATTGTA[C/T]TCTGAAGCATAAGAG | 1130 |
rs752860944 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681253 | TGGGCTAAGAAGACA[A/G]CATGTGTGAGGGAAA | 1130 |
rs752872919 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235852459 | ATGTTGAGGTAATCT[C/G]AGCACTTTGCCGGAC | 1130 |
rs752896052 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753182 | TTATGCAAGAGTATG[C/T]TGTCATATAGAGAGG | 1130 |
rs752903978 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884883 | CTGCAGCCTCAAACG[C/T]CTGGGCTCAGGTGAT | 1130 |
rs752908934 | snp | C/T | 4.94597e-05 | 0.00497266 | intron-variant | LYST | GRCh38.p7 | 1:235755454 | AAAGATTCCCAATTA[C/T]AGTGGAGGGAAGAAC | 1130 |
rs752913280 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769446 | ATAATGAAAAGCCCT[C/T]AGTGCCACCGAAGCA | 1130 |
rs752938038 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759449 | ACATAAGTATCTGCA[A/G]TATTTTGTAACCTGT | 1130 |
rs752944304 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713682 | CTAAACGTCCTACAA[C/T]GCACAGGGCAGCTCC | 1130 |
rs752944449 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235699478 | TTATCTAGTCTATCA[C/T]TGATGGGCATTTGTG | 1130 |
rs752946880 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823400 | TATTATTACCTTTAC[C/T]ATATTTAAAAGTTTG | 1130 |
rs752946998 | snp | C/G | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808735 | CAAAGTTCTGATAAG[C/G]CTTTAAAGCATCCCA | 1130 |
rs752965371 | snp | C/T | 0.000119624 | 0.00773291 | intron-variant | LYST | GRCh38.p7 | 1:235780817 | ATTACAATAAATATA[C/T]CTAAATACATTTACT | 1130 |
rs752981694 | snp | C/G | | | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757386 | AAGCAAAACATCAGG[C/G]AGGATAAGAAGAACC | 1130 |
rs752985483 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791886 | GTGGACTGGGGCTAT[A/G]TGCCAAGATGAAAGC | 1130 |
rs752990332 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | LYST | GRCh38.p7 | 1:235697094 | TTACCTTGTTCCTTG[C/T]TATATGTCATCAGAA | 1130 |
rs753001333 | snp | A/C | 1.65002e-05 | 0.00287225 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809191 | AGCACCGCTCAGGAT[A/C]ATAAACATCTCCATC | 1130 |
rs753002915 | snp | C/T | 3.30213e-05 | 0.00406319 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810070 | ATGGAGAATTGTTCA[C/T]GTTACTGATAACAGA | 1130 |
rs753038724 | snp | C/T | 3.2963e-05 | 0.00405961 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810163 | AATTTTCCAAAGCCA[C/T]AGCATCTGGAGGAGT | 1130 |
rs753055039 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235824577 | CTGGGCATGGTGGTA[C/T]GGTAGAAATATTCAA | 1130 |
rs753064622 | snp | A/G | 0.000165566 | 0.009097 | intron-variant | LYST | GRCh38.p7 | 1:235716693 | CATTTAATAAAGTAC[A/G]AGTAAAAACAAAAGC | 1130 |
rs753067671 | snp | A/G | 1.65012e-05 | 0.00287234 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757388 | GCAAAACATCAGGCA[A/G]GATAAGAAGAACCCC | 1130 |
rs753083496 | snp | A/C | 1.64912e-05 | 0.00287147 | missense, downstream-variant-500B, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751218 | TACTCGCCAGCAATG[A/C]TTTTCCGCTTTTGAA | 1130 |
rs753089428 | snp | C/T | 4.94735e-05 | 0.00497336 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810380 | ATGGGTAATTTTACG[C/T]TGTCGTCTGCTTTTT | 1130 |
rs753101023 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235755429 | AAAAGAAAAGAAAAG[-/AA]AAAAGACAAAAGATT | 1130 |
rs753120847 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806634 | AATATCTGGAACTGA[A/G]GCATCTTTCTGTTGC | 1130 |
rs753135590 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235848643 | GCAAGATTAACCAAG[-/A]AAAAGAAGAGAGAAA | 1130 |
rs753144298 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862414 | GCACCCTGTTCTGAG[C/T]AGCATGATGAAATCT | 1130 |
rs753186347 | snp | C/T | 4.94368e-05 | 0.00497152 | missense | LYST | GRCh38.p7 | 1:235662998 | TGTTTCAAGCGCTGC[C/T]GGTCCTTCCGACACC | 1130 |
rs753189336 | snp | C/T | 1.65479e-05 | 0.0028764 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773972 | ATAATATCTTCACCA[C/T]AGCATCCTTCAAGAA | 1130 |
rs753189554 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235831864 | CAGTTCATATTTATC[C/T]AACTTTAATATATTT | 1130 |
rs753203268 | snp | G/T | 4.94271e-05 | 0.00497102 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734580 | ATAAGCAGTTCTGCT[G/T]TGCCTAGCTCTTCTT | 1130 |
rs753221963 | snp | A/G | 3.2963e-05 | 0.00405961 | intron-variant | LYST | GRCh38.p7 | 1:235804486 | CCAAAGAACACAACT[A/G]TATGTTGTTATTCAT | 1130 |
rs753227275 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235851959 | ATATTTATTGACTAC[G/T]CACCATACTTCGTGG | 1130 |
rs753248220 | snp | C/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787214 | CCTCTGTCCAGAGAC[C/G]CATATGGAGATTTTC | 1130 |
rs753274067 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722552 | GTGTAATGGCGTGAT[C/G]TTGGCTCGCTGCAAC | 1130 |
rs753293453 | snp | A/G | 1.79603e-05 | 0.00299663 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781042 | AAAGGCCTCTTGTGA[A/G]CCAACCTTAGCTCCT | 1130 |
rs753309649 | snp | A/G | 1.6513e-05 | 0.00287336 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806513 | CTTTGAGGCCAGCAT[A/G]AAATTTGCTGAGACT | 1130 |
rs753320077 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818370 | CTCTCAGGGCATGGA[C/T]TCCAGGGCTCAGGCC | 1130 |
rs753328331 | snp | A/C | 3.29973e-05 | 0.00406172 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805912 | GCTGAAACTTCTTCC[A/C]CATTTATGGAAGAAA | 1130 |
rs753330380 | snp | A/G | 4.9498e-05 | 0.00497459 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808510 | GAAGCACGTCCTGAG[A/G]CAAGCACTGGTTATG | 1130 |
rs753341295 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235745543 | ACACATGTAATTACC[A/G]TATGACCCAGTAACT | 1130 |
rs753345121 | in-del | -/TTG | | | intron-variant | LYST | GRCh38.p7 | 1:235877407 | CACTTATGGTCAACT[-/TTG]TTGTTGTTGTTTTTG | 1130 |
rs753348191 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675766 | TCATTCTAGCAAATT[A/T]TTGAACCTGAGGGTG | 1130 |
rs753354686 | snp | A/C | 1.67354e-05 | 0.00289265 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235743984 | ATTTACTTACAATAG[A/C]TACTTTGAATCCTTC | 1130 |
rs753370421 | snp | A/C | 5.32061e-05 | 0.00515754 | intron-variant | LYST | GRCh38.p7 | 1:235762877 | AATTTTTTTTGAAAC[A/C]GCAAAATTTTTAAAA | 1130 |
rs753370767 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235707245 | TATTTACTTTTGCAT[A/C]CCCAGCACCTAGCAA | 1130 |
rs753389200 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235856780 | TTGGAAGCATCACTA[A/G]GCAGAAATTCAGGAA | 1130 |
rs753400214 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235841667 | AAATAAGTGTGGATT[C/G]GATCAAGGGTATAGG | 1130 |
rs753409649 | snp | G/T | 1.65677e-05 | 0.00287812 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809732 | TAGGCATATTCTAAT[G/T]TTTAAAGCTGCTCTA | 1130 |
rs753410269 | snp | C/T | 1.67318e-05 | 0.00289234 | intron-variant | LYST | GRCh38.p7 | 1:235709041 | ACTAACCTTAAAATA[C/T]TCAGGTTCTATCTTA | 1130 |
rs753432463 | snp | A/C | 1.73942e-05 | 0.00294903 | intron-variant | LYST | GRCh38.p7 | 1:235777050 | AGACAAAACTATAAG[A/C]AGTGATTCTTACCCT | 1130 |
rs753434855 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235773769 | TGAAACTTAAAAATG[C/G]TTAAGATGGTAAATT | 1130 |
rs753437533 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731152 | GCCATGAGGTTGGAT[A/G]GTAGATGGGGTCATA | 1130 |
rs753439294 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235869740 | AAAAATCTGCATTGG[C/T]TCTCCGCTTCTCTCA | 1130 |
rs753441057 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740089 | AATACAGGCTAAATA[C/T]GCTTCTGTCTTGGGA | 1130 |
rs753456886 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235696476 | CAGTAAGTAGGAAGA[A/G]TTCTTTTGTTTCTAG | 1130 |
rs753458872 | snp | A/G | 1.88906e-05 | 0.00307326 | intron-variant | LYST | GRCh38.p7 | 1:235752220 | TTTATAAGAAAAAGA[A/G]CAAATAATTTAAGAC | 1130 |
rs753460525 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235732117 | AGTTATGATCATTAT[A/G]ATCATTTTTCTATAA | 1130 |
rs753481684 | snp | G/T | 3.71962e-05 | 0.00431239 | intron-variant | LYST | GRCh38.p7 | 1:235757240 | TTACATATATATTTA[G/T]TTTTCTGAATTAAAA | 1130 |
rs753504614 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235683028 | ATTGTAAAAAATATG[C/T]CAGAAGAAACATAGA | 1130 |
rs753506244 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789687 | AAATACTCCCTGTAG[C/T]GATGACAATAGTTTT | 1130 |
rs753525163 | snp | A/G | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868799 | CTCCCGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 1130 |
rs753535425 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810284 | TCTATGCTTATTCAT[C/T]GCTATGCCTTTTTCA | 1130 |
rs753541871 | snp | C/T | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806379 | TTCTGAGTCATTGGC[C/T]GACTCCCTGTCAGAC | 1130 |
rs753548259 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715982 | CTCCCATAGCTTCTG[C/T]CTGGTTCTGATAACA | 1130 |
rs753550468 | snp | C/T | 0.000117204 | 0.00765428 | intron-variant | LYST | GRCh38.p7 | 1:235733950 | ATAAAATTTATTATT[C/T]CTCACCTAACATTGT | 1130 |
rs753558003 | snp | A/T | 1.65669e-05 | 0.00287805 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762786 | GGCTCATAAGGGACC[A/T]TCCTCCACTGCTGGA | 1130 |
rs753561017 | snp | A/G | 0.000132901 | 0.00815065 | intron-variant | LYST | GRCh38.p7 | 1:235830135 | GGACTTTATCTCAAG[A/G]AGGCTTCAGAAACTA | 1130 |
rs753563646 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771626 | ATCTGAAAGTATATA[C/T]TTATTCAGAGTGAGA | 1130 |
rs753570779 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235825327 | CACTACTTCCATCTG[C/T]TTTTGTACTAGAAGC | 1130 |
rs753578907 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235684469 | TGTAGGGGAAGTCAG[A/C]AAGGGGAGCTCAGAA | 1130 |
rs753593464 | snp | A/C | 1.66707e-05 | 0.00288705 | intron-variant | LYST | GRCh38.p7 | 1:235801117 | AAAGAGAAAAGCGAA[A/C]GATTACTTGTATTCC | 1130 |
rs753599415 | snp | A/G | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660845 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 1130 |
rs753604024 | in-del | -/AAT | 1.65184e-05 | 0.00287384 | intron-variant | LYST | GRCh38.p7 | 1:235733699 | GAAAGAGACTAAACA[-/AAT]AATAAGATTGTCCAT | 1130 |
rs753613822 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881102 | GCTGGAACTGGGGTT[C/T]CTAACTCCAAATTTC | 1130 |
rs753624235 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758231 | GGGGATATCTCATCA[C/T]CAAAGCAAGGTCATC | 1130 |
rs753643977 | snp | C/T | 1.65452e-05 | 0.00287616 | intron-variant | LYST | GRCh38.p7 | 1:235723980 | GTATAGTTACAGTGG[C/T]CCATGAGCACTTAAA | 1130 |
rs753647581 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235882013 | AAAAATGGGTAAGAC[A/G]ATAAATTTTATGTTA | 1130 |
rs753664265 | snp | C/T | 1.67273e-05 | 0.00289195 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752129 | TGCTATGAAAAGTTG[C/T]TGTATATCACAAGCA | 1130 |
rs753670444 | in-del | -/TAA | | | intron-variant | LYST | GRCh38.p7 | 1:235689049 | CAACAACAACAACAA[-/TAA]TAATATCCTAGCTGA | 1130 |
rs753678420 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724070 | TGTTCTGCCATTTGT[C/T]AGAAAGATTTCTACA | 1130 |
rs753687156 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772057 | GTGAGACTTCATCTC[C/T]ACAAAAAAAAATTAA | 1130 |
rs753692015 | snp | A/T | 3.29511e-05 | 0.00405887 | synonymous-codon | LYST | GRCh38.p7 | 1:235693431 | AATATTATCAGCATA[A/T]CCCCAGCTCAGGATG | 1130 |
rs753698025 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826983 | GTGTATTTGTCACTA[C/T]TCATCTAACTGCATA | 1130 |
rs753722157 | snp | A/G | 1.65026e-05 | 0.00287246 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770256 | GTGATCTGCTCTGAT[A/G]AGGACTTCTAGAGCT | 1130 |
rs753723846 | snp | A/G | 1.65485e-05 | 0.00287645 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759037 | GGCAAAGTTTTCCCA[A/G]TCATCAGTGTTTCTA | 1130 |
rs753725793 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711589 | TGTTAGTTGGCATCA[C/T]AGAAAATTTGATTTT | 1130 |
rs753728456 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717376 | AGTATGTATGCATGC[G/T]TACAAATCTGTCAGT | 1130 |
rs753730677 | snp | C/G | 1.64977e-05 | 0.00287203 | intron-variant | LYST | GRCh38.p7 | 1:235733794 | AAATCTAATGGATTC[C/G]TAAAATACATGCCTT | 1130 |
rs753748324 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702137 | CATTCTACTATCTTA[C/T]GCTGTTTTTATAACG | 1130 |
rs753751664 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813897 | GTGGGAGAGGGGGTC[A/G]CATGATGACACAATC | 1130 |
rs753756469 | snp | C/T | 1.65078e-05 | 0.00287291 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809650 | GATACTTTGAAAACA[C/T]AAAATCTTCCTGAAC | 1130 |
rs753761665 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672915 | TGTCTTCCACCCTTT[A/G]CTCACTCCCTCAAGA | 1130 |
rs753776980 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235773567 | AAGACAAATACTATA[C/T]GATCCTACTTATATG | 1130 |
rs753787891 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702889 | TGGAACAGCTGACGG[G/T]GAGTCTGCCCGTAGG | 1130 |
rs753800553 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823707 | TGTGTTTTCTCTAGC[C/T]CCCGTGTTTTTTCAT | 1130 |
rs753801553 | snp | G/T | 1.66244e-05 | 0.00288304 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808903 | AGTCAACAGTACAAA[G/T]ATTACAAGCTGCTTT | 1130 |
rs753801757 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235840693 | GTGAGTGGCATGGTC[-/A]ATCTTGAACACATAG | 1130 |
rs753802621 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235788335 | GGCTAATTTTTGTGG[-/T]TTTTTTGTTTTTTTG | 1130 |
rs753809133 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235744895 | GAGAACCCATCTCAA[-/A]AAAAAAAAGAAAAAA | 1130 |
rs753833058 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703126 | TCACTCATGGTCTCA[C/G]TGAGATCAGAAGTAT | 1130 |
rs753845145 | snp | C/T | 1.65091e-05 | 0.00287303 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759095 | GCTGCAGATCCGTTC[C/T]GTGAAGGAAAAGCTA | 1130 |
rs753846652 | snp | C/T | 0.000116777 | 0.00764033 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715157 | TTGTTGTTGTTGTTT[C/T]TGATGACCCAACATG | 1130 |
rs753848847 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235742242 | GGTGGATCACCTGAG[C/G]TCAGGAGTTCAAGAC | 1130 |
rs753856790 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235874150 | ATTCTGAATATTTAC[A/C]GTTTACCATTCTATA | 1130 |
rs753860672 | in-del | -/G | 1.65456e-05 | 0.0028762 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716753 | CTTTTTCTTTATACT[-/G]AACAGCTATAGGTTT | 1130 |
rs753867118 | snp | C/G | 0.000186968 | 0.00966691 | intron-variant, nc-transcript-variant | LYST, MIR1537 | GRCh38.p7 | 1:235853054 | AAAACTGACTAATTA[C/G]AGCTGTACTTAGTGC | 1130 |
rs753871850 | snp | A/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235846151 | TGCACCAGAAAAGGC[A/G/T]CTGGTATCCATGGCT | 1130 |
rs753905813 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771916 | AAGGTTTTTTAGTTT[-/G]GTTTTTTTTTTTTTT | 1130 |
rs753908011 | snp | A/C | 0.00012607 | 0.00793847 | intron-variant | LYST | GRCh38.p7 | 1:235759620 | AAGAGTAGATACAAA[A/C]ATACTACTTAAAAAT | 1130 |
rs753922068 | snp | C/T | 1.66065e-05 | 0.00288149 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808832 | TAAACTTGAGGAGAG[C/T]TCAGCATCACATAAG | 1130 |
rs753955192 | snp | C/T | 5.47141e-05 | 0.00523011 | synonymous-codon | LYST | GRCh38.p7 | 1:235712076 | ACGGTTAACTAGGAA[C/T]TCTGGAAGATAGAAA | 1130 |
rs753969752 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235732048 | AAACATACCAAAATA[-/C]TGGTAGCGGTTGTTG | 1130 |
rs753970499 | snp | A/G | 1.65548e-05 | 0.002877 | intron-variant | LYST | GRCh38.p7 | 1:235730817 | GTTGTATATTCATGA[A/G]AGAGTGAAGGTCTAT | 1130 |
rs753980951 | snp | A/C | 6.59245e-05 | 0.0057409 | intron-variant | LYST | GRCh38.p7 | 1:235755460 | TCCCAATTATAGTGG[A/C]GGGAAGAACACACTT | 1130 |
rs753991722 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235725584 | AGATTTAGGTTAAAT[A/C]CATGTCTGGATGGCC | 1130 |
rs753992680 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235667759 | GCAACCTCCGCTTCC[C/T]TCAAGCGATTCTCCT | 1130 |
rs753997952 | snp | C/T | 1.65233e-05 | 0.00287426 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746452 | CGTTGCATCATCACA[C/T]GAAGCTCATCATTTG | 1130 |
rs754009518 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835510 | GCTGAGGGATTTCTC[C/T]AATGCTCTTAAACTG | 1130 |
rs754011092 | snp | C/G | 1.70133e-05 | 0.00291657 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780964 | TTTGGAGTAGTCATT[C/G]ACTGGCTTGCCATAC | 1130 |
rs754024243 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235839133 | CCTGGCCTCATTTTC[A/G]TTCTCTACATATAAA | 1130 |
rs754055657 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235784225 | AAAGATACTAGAGAA[C/T]CAAGTTTAAGTCAAC | 1130 |
rs754073198 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235700284 | GAGACTACCATCAGA[A/G]TGAACAAGCAACCTA | 1130 |
rs754074033 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820660 | ACAGGGGTGAACCAC[C/T]ACATCCAGCCTAATA | 1130 |
rs754077164 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235766739 | ATAGTGCCTTGCATA[C/T]AGGTAAGCCCCATAT | 1130 |
rs754079124 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235838544 | TTTAAAAATGATCTC[-/TA]GAGTCTTTTGTGGAA | 1130 |
rs754084620 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821719 | TCTTCTGTTTAACAA[C/T]CCTTTAAAAATGCAA | 1130 |
rs754085798 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755531 | GATGAAGCATTCTAA[C/T]AATTCTTGAGTTCCT | 1130 |
rs754092068 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235710323 | CTGCATGGTTGATTT[A/C]GGATGGACTGGCTGA | 1130 |
rs754095504 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | LYST | GRCh38.p7 | 1:235770123 | TATTAAACAACTGTG[A/G]AATATATTTCCAAAA | 1130 |
rs754138948 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806649 | GGCATCTTTCTGTTG[C/T]TCCCCTAGGCTGATT | 1130 |
rs754141501 | snp | C/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853407 | GTTCCTATATTTATT[C/G]TGTATTATGCATTTA | 1130 |
rs754157908 | snp | C/T | 1.65534e-05 | 0.00287688 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809009 | CTGAAAATTTTTCAG[C/T]GCTGGCAATTTAAAA | 1130 |
rs754178725 | snp | A/G | 3.29772e-05 | 0.00406048 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809317 | ATTCACATCGTCTGT[A/G]CCTTTTTCTTGTACA | 1130 |
rs754190641 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235669073 | TGTGGTATAATGAAA[A/C]ATAAGTATTTGGTCT | 1130 |
rs754201076 | snp | C/T | 8.29772e-05 | 0.00644063 | intron-variant | LYST | GRCh38.p7 | 1:235773995 | TTCAAGAAGGGTCTA[C/T]AGAAAATTAGCATTA | 1130 |
rs754202081 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702757 | CATACCGGATAGGTG[A/G]TTTCTTTGACCTGTT | 1130 |
rs754203277 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669854 | TTCTTTGTTCAAAAC[A/G]CCAAGAACCTGGACA | 1130 |
rs754209034 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698733 | AAAAATTTAACTGGG[C/T]GTGGTGGCGGGTGCC | 1130 |
rs754209450 | snp | C/T | 6.59261e-05 | 0.00574097 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751312 | TTGCGGTGGTCCTTA[C/T]AAATTCCATAGCAGC | 1130 |
rs754212379 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785228 | TAGGCCTTCCCTGAT[C/T]CACCCATCGTAAGTG | 1130 |
rs754217713 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857487 | ATAGGTGGTATATGA[A/G]AGCTTAGAAATAGAT | 1130 |
rs754218446 | snp | C/T | 1.65255e-05 | 0.00287445 | missense | LYST | GRCh38.p7 | 1:235697230 | CACTGGGGGAACCCA[C/T]GTATTCCCCCCATTT | 1130 |
rs754220302 | snp | A/G | 4.55602e-05 | 0.00477263 | intron-variant | LYST | GRCh38.p7 | 1:235734693 | TTTTTTAGTCATTTA[A/G]AATTTTAATTCTTAC | 1130 |
rs754236811 | in-del | -/AGA | 1.72844e-05 | 0.00293971 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792112 | ATTTTCAGAATACCC[-/AGA]AGAAGAATTTTCTAG | 1130 |
rs754243108 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235748879 | GTCTGGTGTGTGGCC[A/G]TAATGCAAGCTGCAG | 1130 |
rs754248132 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865364 | CTCTGTAGTACTTAA[C/T]ACCATCTGACACAGC | 1130 |
rs754248708 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235750020 | ATACAAAAGAAACAG[C/G]AGGGGTAGTAAAGGT | 1130 |
rs754256855 | in-del | -/TAAC | 5.36879e-05 | 0.00518084 | intron-variant | LYST | GRCh38.p7 | 1:235766325 | AAAGAATTGTCAACT[-/TAAC]TAAGATTTTTCATTT | 1130 |
rs754293166 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829278 | AATTTGTATTTGCTA[C/T]GTTCCTTAGCTTACA | 1130 |
rs754300450 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235713527 | ATATATTAAACCTGT[-/G]GTTCTCAACCAGTAG | 1130 |
rs754303812 | snp | G/T | 3.30017e-05 | 0.00406199 | intron-variant | LYST | GRCh38.p7 | 1:235787393 | AGAAAAAGAGAAAAG[G/T]CATAGGCTGAAAACA | 1130 |
rs754309233 | snp | C/T | 3.30218e-05 | 0.00406323 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759502 | AGTCAGTTTTTGTGA[C/T]TGCGTTAGTAGTGAA | 1130 |
rs754314844 | snp | G/T | 3.73741e-05 | 0.00432269 | intron-variant | LYST | GRCh38.p7 | 1:235805700 | TGTGTGTATATATAT[G/T]TATATATATTACATA | 1130 |
rs754315760 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235686589 | TACCCAGAGGTTATC[A/G]GAATGTTGGACATTA | 1130 |
rs754329253 | in-del | -/CAGAGGA | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852852 | AGATTTCCCAAAAGT[-/CAGAGGA]CTTAACAGCTAGGTC | 1130 |
rs754332329 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718897 | TTTAAAAAGTATCAC[C/T]ATGACCTTACGTTTC | 1130 |
rs754340675 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681355 | GTGGTGAGGTAGAGG[A/G]GGCAGTGAGGCAGAG | 1130 |
rs754344647 | snp | G/T | 1.65389e-05 | 0.00287562 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738627 | AATGTTACTGGTGTC[G/T]CCCTCAAGACTCTGC | 1130 |
rs754347082 | snp | C/T | 3.33656e-05 | 0.00408432 | intron-variant | LYST | GRCh38.p7 | 1:235729565 | ATAAGGCAGGGTGAA[C/T]ATGTGCAAAATTCTT | 1130 |
rs754380320 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235851189 | ATGTATATGTGTGTG[-/TA]TATATATATATATGA | 1130 |
rs754383530 | in-del | -/CAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235872295 | AGTGACATTCTGTCT[-/CAAA]AAAAAAAAAAAAAAA | 1130 |
rs754397138 | snp | C/T | 1.7903e-05 | 0.00299185 | splice-donor-variant | LYST | GRCh38.p7 | 1:235774912 | TTTTATGAAGACATA[C/T]CTTCAAAATGTAAAA | 1130 |
rs754404744 | snp | A/G | 1.65806e-05 | 0.00287924 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806720 | CATTTAAGCAATTTA[A/G]TTCGATTATTTGACT | 1130 |
rs754405330 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864315 | AACGTGAATGTCTAA[C/T]TTTATTGTCTTCTAA | 1130 |
rs754409613 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235804429 | AATGACATTCATCAG[C/T]GTCCTAGTGTCATCC | 1130 |
rs754430305 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838343 | AACTCTCCTTCATGT[C/T]CCCAAGTATAGAATG | 1130 |
rs754434491 | snp | A/T | 1.76505e-05 | 0.00297068 | intron-variant | LYST | GRCh38.p7 | 1:235788677 | TACATTATCTATTCA[A/T]GGGAGGCTGAGGATA | 1130 |
rs754435364 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, stop-lost, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751339 | CAGCCTGGAGAACTC[C/T]AAGCTGTAGTGCAAC | 1130 |
rs754448845 | snp | C/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800956 | GCAAGCACATCAAGT[C/T]TGGCTTTACTAGCAG | 1130 |
rs754456959 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235696562 | TTTTCCAGTGTCTAG[C/T]TGACATTTAGAAACA | 1130 |
rs754462976 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235820290 | AGATGGCTAGGGTTC[-/A]AGGACTTCTGGATGA | 1130 |
rs754474476 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235699581 | TGATTTATATTCCTT[-/T]GAGTATATACCCAGT | 1130 |
rs754475583 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235666766 | CATGAGTAGGCTACA[C/T]TTCAACCTTTCTTTT | 1130 |
rs754477010 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235839239 | TTTATATGTGTGGGT[C/G]TATGTGTGCATATAT | 1130 |
rs754478774 | in-del | -/ATGTGT | | | intron-variant | LYST | GRCh38.p7 | 1:235730567 | TATATACATATTTAT[-/ATGTGT]GTGTGTGTGTGTGTG | 1130 |
rs754483685 | in-del | -/CC | | | intron-variant | LYST | GRCh38.p7 | 1:235723705 | AGCATATGCAACTTT[-/CC]CCCCAACAGTTTTTC | 1130 |
rs754483850 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235703070 | AACACTTTGTTTTAT[-/A]TTCTAGGTTATGGAA | 1130 |
rs754497817 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720779 | CATGTTTGTTTAAGT[A/G]AGTCAAATATTCAAA | 1130 |
rs754500418 | snp | A/T | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852729 | AATTATTTTAAAATG[A/T]GAATCCATTCTACAA | 1130 |
rs754502734 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235746831 | GGCTCAAATAGTTCA[A/G]AACATTTTGATAAAA | 1130 |
rs754510251 | snp | C/G | 1.65127e-05 | 0.00287334 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809445 | GGAGGAACTCCATCT[C/G]TTAAAACCAGCCATT | 1130 |
rs754557041 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235719180 | TGTGCCACCACGGCC[A/G]GCAAATTTTGTATTT | 1130 |
rs754562005 | snp | A/C | 1.99998e-05 | 0.0031622 | intron-variant | LYST | GRCh38.p7 | 1:235697292 | AATGAAGAAAAATAA[A/C]AAGTATGGCTTTTTA | 1130 |
rs754564404 | snp | A/C | 1.67536e-05 | 0.00289423 | intron-variant | LYST | GRCh38.p7 | 1:235664441 | TGAATGAAATCAAAA[A/C]AAGAGAATCCAAATT | 1130 |
rs754566788 | snp | C/G | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867162 | GCTGCAGCCGGGGCC[C/G]GGTCTGGGTTTCTCA | 1130 |
rs754571229 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235729612 | TAGTAACAATTCACC[A/G]GCTGTCTCTCTAGAT | 1130 |
rs754573535 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235797629 | CGTATACAAAATTTA[A/T]CTCAAAATGAATTCA | 1130 |
rs754576759 | snp | A/G | 1.68383e-05 | 0.00290153 | intron-variant | LYST | GRCh38.p7 | 1:235804670 | ACAGACAAGTTCTAA[A/G]GTAAAATAAAAGAGA | 1130 |
rs754580179 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665405 | ACCTGAAGTCAGGAG[A/T]TCGAGACCAGCCTAG | 1130 |
rs754584187 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865647 | CTATCAGAAAAAGAG[C/T]TGTTGGCCACTTAAC | 1130 |
rs754588229 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235789720 | AAAAGAAGAGTTAAG[A/G]TCACTGATTATTTTG | 1130 |
rs754589763 | snp | C/T | 1.65548e-05 | 0.002877 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738540 | GAAAGGCTGGGAGTT[C/T]ACACATTAAGCTGTC | 1130 |
rs754596305 | snp | A/C/G/T | 0.000346217 | 0.0131528 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809336 | TTTTCTTGTACACAT[A/C/G/T]GAATGATGAAGTTGC | 1130 |
rs754608896 | snp | C/T | 1.93485e-05 | 0.00311029 | intron-variant | LYST | GRCh38.p7 | 1:235830428 | CTCATGACCGAGCTA[C/T]AAAATAAGTATTACA | 1130 |
rs754610267 | in-del | -/TGTATGGAGTAAAGCAAA | 1.65571e-05 | 0.0028772 | intron-variant, splice-acceptor-variant | LYST | GRCh38.p7 | 1:235738596 | AGATTCTAGTGTGCC[-/TGTATGGAGTAAAGCAAA]TGTTACTGGTGTCTC | 1130 |
rs754612949 | snp | A/G | 1.9742e-05 | 0.00314175 | intron-variant | LYST | GRCh38.p7 | 1:235806784 | TACCCTGTGAAAGAA[A/G]AAAAGCATGTAAAAA | 1130 |
rs754616030 | snp | A/G | 1.64732e-05 | 0.0028699 | stop-gained, intron-variant | LYST | GRCh38.p7 | 1:235702776 | CTTTGACCTGTTCTC[A/G]GGTCTCCCTGAAAGC | 1130 |
rs754616998 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235697683 | ATGTAGCACAGGAAA[C/T]CTCACTCAGCTATGA | 1130 |
rs754625439 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732292 | AGAGATGAAAACTTT[C/T]ATGTTTACTTTCTTT | 1130 |
rs754648430 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845862 | GCTGCTGAGCTCATA[C/T]ACACCTAGCCCCACC | 1130 |
rs754656138 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235878098 | GCCCACTTAATAATG[C/T]AATCTTCTGGATCTT | 1130 |
rs754673243 | snp | C/T | 1.66139e-05 | 0.00288213 | intron-variant | LYST | GRCh38.p7 | 1:235766034 | GTGGGAAGAATAAAA[C/T]AAAAGTGGAAATAGC | 1130 |
rs754673551 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235877026 | AGGGTCTGGCATCCA[G/T]ATTTGCTCCTTACCT | 1130 |
rs754676044 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235791196 | CTGAGGCAGGAGAAT[A/C]GCTTGAACCTGGGAG | 1130 |
rs754680391 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235825619 | TATTTAGAATAAATT[C/T]AACCAAACAACAGGC | 1130 |
rs754689788 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883658 | GCTTTTTCGTTTGGT[A/C]ACGGGGCTAGGAAAT | 1130 |
rs754704932 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235795309 | GAAATGGTCAGGTGT[A/G]TACAGGCTTTTAGCA | 1130 |
rs754708997 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684479 | GTCAGAAAGGGGAGC[G/T]CAGAAGATTAAAGGT | 1130 |
rs754709482 | in-del | -/TC | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750962 | GGGGCAGAATCTGTG[-/TC]TGTTTTTTTCATCAT | 1130 |
rs754729724 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235716026 | TGAATTTTCAAGAGT[C/T]ACTTCTTGATTTCCA | 1130 |
rs754729906 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235816705 | GCACAGTACTGGTAC[-/A]AAAAACAGACACAGA | 1130 |
rs754734457 | snp | G/T | 1.65605e-05 | 0.0028775 | intron-variant | LYST | GRCh38.p7 | 1:235677626 | TTCTGATGGCTGAAA[G/T]TTTAAAATTAAGTAT | 1130 |
rs754736193 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235812732 | CTGATAAGTGTTTCT[C/G]CTTCTTTATACATTT | 1130 |
rs754738149 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844849 | ACATATCAGTTGAAC[C/T]GTACAATATTTAAGC | 1130 |
rs754743119 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817181 | TGAGATACCATCTCA[C/G]ACCAGTCAGGATGGC | 1130 |
rs754759720 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772125 | AGCTACTTGGGAGGC[C/T]GAGGTAGGAGGACCA | 1130 |
rs754761237 | snp | C/T | 6.5937e-05 | 0.00574144 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777208 | GAGCTGAAGGGTCTT[C/T]GAGAGAGTTGGGTTT | 1130 |
rs754762666 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672334 | AGAAGGTAGCAAAAG[A/T]CAAGAGACCTAAGGT | 1130 |
rs754782150 | snp | C/T | 1.66291e-05 | 0.00288345 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744134 | CTGGAGTTCTCAAAA[C/T]GTCAATAATGTCTGA | 1130 |
rs754785961 | snp | C/T | 1.65051e-05 | 0.00287267 | intron-variant | LYST | GRCh38.p7 | 1:235677447 | TGGATATATTAAAAA[C/T]GCTATGTTTGATTTG | 1130 |
rs754801644 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235786904 | GGGCCTGTCGTGGGG[G/T]GGGGGGAGGGGGGAG | 1130 |
rs754824059 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813909 | GTCGCATGATGACAC[A/C/T]ATCAGATTTGCTGAA | 1130 |
rs754824089 | snp | C/T | 3.33072e-05 | 0.00408075 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808736 | AAAGTTCTGATAAGC[C/T]TTTAAAGCATCCCAT | 1130 |
rs754837559 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235702152 | TGCTGTTTTTATAAC[A/G]AAGAATTGAGTTGAA | 1130 |
rs754849200 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235740684 | TATAAAGAAATCACA[A/T]TGTGTTTGTACATTC | 1130 |
rs754860951 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806200 | AGCCTATAAAACTGT[C/T]TCTGGAACACTGAAC | 1130 |
rs754869577 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844982 | CTCCTGGGATCATGG[C/T]GAAGGGAGGCAGGAC | 1130 |
rs754879925 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235871569 | CAATAGTAACATAGG[A/C]AAATAACAATACTAA | 1130 |
rs754889529 | snp | A/C | 1.68043e-05 | 0.0028986 | intron-variant | LYST | GRCh38.p7 | 1:235758924 | GTAGAGAGTCTTTAA[A/C]GAATAGTAAAATAAA | 1130 |
rs754895438 | snp | C/T | 3.45519e-05 | 0.00415629 | intron-variant | LYST | GRCh38.p7 | 1:235800419 | TACAAAATTAAATTA[C/T]TTACCTCACAGAAGC | 1130 |
rs754898913 | snp | C/T | 6.71603e-05 | 0.00579445 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810521 | TATATCTGCTGAGAG[C/T]GGTAGGTTAAAATCT | 1130 |
rs754911934 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235799416 | CTTGGCAAACACCTC[C/T]TTAACCACATGATCA | 1130 |
rs754914593 | in-del | -/TGTGTGTGTA | | | intron-variant | LYST | GRCh38.p7 | 1:235730606 | GTGTGTGTGTGTGTG[-/TGTGTGTGTA]TATGTAAACTAACAA | 1130 |
rs754926570 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689708 | AATGTGTTAATTAGC[C/T]TGACTGTAGTAATCA | 1130 |
rs754928599 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703226 | AATTAGCTTTTAATT[G/T]AAGATCTGAGAATAT | 1130 |
rs754949253 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235857330 | GAGATTACTAGCCTA[A/C]GATGACTTTCTCTAG | 1130 |
rs754952723 | in-del | -/AAT | | | intron-variant | LYST | GRCh38.p7 | 1:235726492 | AAGTGCTCTGCATGA[-/AAT]ACATCTGTATGGGTC | 1130 |
rs754974224 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789848 | GTAGGACAAAACCAG[-/T]TGTGTACCTAGGAAT | 1130 |
rs754974393 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235724723 | ACTAATTTGTTTACT[C/G]TCTCTATAGTTTTGC | 1130 |
rs754981708 | snp | A/G | 3.32878e-05 | 0.00407956 | intron-variant | LYST | GRCh38.p7 | 1:235733473 | TAAATCTTCATGGAA[A/G]ACAATTTTAACTGAC | 1130 |
rs754991654 | snp | A/G | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810400 | GTCTGCTTTTTCGAA[A/G]AACATTTACTTTTGC | 1130 |
rs755006492 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235742257 | GTCAGGAGTTCAAGA[C/T]CAACCTGGACAACAT | 1130 |
rs755032963 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235783196 | TTAATGAGAAATTCA[A/C]CTTTGTGTATATTTA | 1130 |
rs755041248 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869955 | ATTTGTTTTCTCCAC[A/G]TGGCTGCAGTTGTTA | 1130 |
rs755056767 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235784361 | GTAAAAAAACAGAGT[C/G]ATATGTGAATCAAGT | 1130 |
rs755060438 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235725638 | AGTTCTCATGCTTCC[A/G]AGTCATTCAGCAAAG | 1130 |
rs755066007 | snp | A/T | 1.66012e-05 | 0.00288103 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809785 | TAAGATTTTCTGGCA[A/T]CATCTCTGCAGTACT | 1130 |
rs755082237 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon | LYST | GRCh38.p7 | 1:235677509 | TATGATGCAGGTTCC[A/G]TCTCTGCTCACACTT | 1130 |
rs755085510 | snp | C/T | 3.32077e-05 | 0.00407465 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809910 | CTCTCCAAGTTGTCG[C/T]TCAGACTGCAGCAGT | 1130 |
rs755085625 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235835557 | TCTGTAGTTTACAAA[A/G]CCTCACTTGAATATC | 1130 |
rs755094958 | snp | C/G | 3.30229e-05 | 0.0040633 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724156 | TCCAGGAAAATGATG[C/G]TGGTTCCAACTCTCC | 1130 |
rs755098509 | snp | C/G | 3.30306e-05 | 0.00406377 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806509 | GCTTCTTTGAGGCCA[C/G]CATAAAATTTGCTGA | 1130 |
rs755106258 | snp | C/T | 7.03779e-05 | 0.00593161 | intron-variant | LYST | GRCh38.p7 | 1:235791632 | ACTACCACATTTTTA[C/T]GGCTCAAGGAAAATT | 1130 |
rs755119451 | in-del | -/CTT | 3.2956e-05 | 0.00405918 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806595 | TACAGAGGACAACTC[-/CTT]CTGTTCAATGTCTAT | 1130 |
rs755127014 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734543 | AGGGATGCACTTGTG[A/G]CCACATAACTTCAAA | 1130 |
rs755129254 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235766773 | TGTTAGTGATAAACT[A/G]CAATCACTACTATTA | 1130 |
rs755134245 | snp | G/T | 3.30093e-05 | 0.00406246 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753177 | GAGCATTATGCAAGA[G/T]TATGTTGTCATATAG | 1130 |
rs755137786 | in-del | -/A | 0.000493143 | 0.0156948 | intron-variant | LYST | GRCh38.p7 | 1:235800396 | AGTTCCCTGAAGATT[-/A]AAAAAAATACAAAAT | 1130 |
rs755151435 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235882752 | AGAAGGAGAGAAAGA[A/G]TAAGTCCATGTTGGA | 1130 |
rs755151833 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235850892 | AGATGTTGGCATGGA[C/T]GTGGTGAACAGGGAA | 1130 |
rs755173231 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830333 | CTTCTTCCTCCCTGG[C/T]CTCCACCCTCTGGAC | 1130 |
rs755173955 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820709 | TTAAATCTGTATCTT[A/G]ACATGCTAATTAAAT | 1130 |
rs755177244 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669190 | GACTACATAGCTTCA[C/G]TCTAGAGGCTGGTCA | 1130 |
rs755199570 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235698734 | AAAATTTAACTGGGC[A/G]TGGTGGCGGGTGCCT | 1130 |
rs755212068 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759360 | ACTCACAGCTACTGA[C/T]GAATGCGTCCTCTTT | 1130 |
rs755212070 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235857896 | AAGTCAGTATTCTCC[C/T]AGTTTCCCAAGATGA | 1130 |
rs755219468 | snp | A/G/T | 3.29882e-05 | 0.00406118 | intron-variant | LYST | GRCh38.p7 | 1:235728060 | TATGTAAATACAGAC[A/G/T]TAAGCCTCTACTCAC | 1130 |
rs755223090 | in-del | -/TGTG | | | intron-variant | LYST | GRCh38.p7 | 1:235730568 | ATATACATATTTATA[-/TGTG]TGTGTGTGTGTGTGT | 1130 |
rs755227090 | snp | A/G/T | 3.31539e-05 | 0.00407137 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744036 | TTTCTGAAATGGATT[A/G/T]AAAACAGAAGACTGT | 1130 |
rs755237870 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711364 | CTACTGATGATTCAA[C/T]AATCAATCAAACAAC | 1130 |
rs755254973 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235793004 | CCCACTACAAAGTAG[A/C]TCCAAAGTTTTCTGT | 1130 |
rs755263433 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235821754 | TATTCTTAGCTTGTA[C/T]ATTGTACAAAACAAG | 1130 |
rs755285393 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685902 | GAAGAACCTGGGAGT[C/T]ACCCTATGCTAGAAA | 1130 |
rs755287779 | snp | C/T | 1.65266e-05 | 0.00287455 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793570 | GAACATGTTCTTGAA[C/T]TCATCAAAGATACCA | 1130 |
rs755294712 | snp | A/G | 1.67153e-05 | 0.00289091 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753081 | CTGCTACTGTATTAC[A/G]TAACACATAGAGTAG | 1130 |
rs755297498 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235862335 | AGGTTTCAGTTACCT[A/G]AGGTCAACTGTGGTC | 1130 |
rs755297999 | in-del | -/AA | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740411 | AACCTCTTTCCAGTC[-/AA]TTCCCTTTCTCACCG | 1130 |
rs755302318 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791792 | TCTCAGCTTCATGGA[C/T]ACACTCCACATTAAA | 1130 |
rs755321635 | snp | A/C | 1.71141e-05 | 0.00292519 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746499 | CATCAGAAGCGATTC[A/C]GTTTGAGCAAGGGGA | 1130 |
rs755329844 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675004 | TACCAAAACCTCTCT[C/T]GATTCTCCCCCGCCC | 1130 |
rs755340353 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235778581 | GTTTCACCATGTTGG[-/C]CAGGCTGGTCTCGAA | 1130 |
rs755381098 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672281 | CATTAGGGAATAACC[A/G]TGACTTTGGATAAGA | 1130 |
rs755381657 | snp | C/T | 1.64958e-05 | 0.00287187 | synonymous-codon | LYST | GRCh38.p7 | 1:235697087 | TTTTATTTTACCTTG[C/T]TCCTTGCTATATGTC | 1130 |
rs755387370 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235876100 | TGGTGGCAGCTCCTA[C/T]AGTCCCAGCTACTCA | 1130 |
rs755397797 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810265 | GATGCAGCAGATGGG[A/G]CCTTCTATGCTTATT | 1130 |
rs755415388 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235794663 | TAGAGAATAGAAGCC[A/C]TATTTAAGCAACATA | 1130 |
rs755421451 | snp | A/G/T | 5.0284e-05 | 0.00501397 | intron-variant | LYST | GRCh38.p7 | 1:235715381 | AACGGTGAATCCAGA[A/G/T]AATTCATGATTGTGG | 1130 |
rs755423191 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235849426 | TACTGAATGGGGAAA[A/G]GTTGAAAGCATTCCC | 1130 |
rs755428649 | snp | A/G | 3.29832e-05 | 0.00406085 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734459 | GGAATCTCCTAAGAA[A/G]GTACTATGGTTTCAT | 1130 |
rs755435300 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235877164 | ACTGACATGCTATCC[A/G]TATAACCGAGTGGTT | 1130 |
rs755445009 | snp | A/G | 3.8025e-05 | 0.00436017 | intron-variant | LYST | GRCh38.p7 | 1:235746573 | TCCCAGTGTTAATAA[A/G]GATCAAGGAAACTAT | 1130 |
rs755471198 | snp | C/T | 1.65847e-05 | 0.0028796 | intron-variant | LYST | GRCh38.p7 | 1:235716680 | AAACACAATTTTTCA[C/T]TTAATAAAGTACGAG | 1130 |
rs755475279 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235776904 | CCTTAATCATCTATG[G/T]CAGAAAGCTTAATAA | 1130 |
rs755475389 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874696 | AATTTAAATAATCTT[C/T]CTTTTATGATACAGA | 1130 |
rs755484543 | snp | G/T | 1.64923e-05 | 0.00287156 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662901 | AACAAATCTAGTTTG[G/T]AGTTAAAGTGCTTTG | 1130 |
rs755494134 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720673 | TACCTGTATATCAAC[A/G]GATCATTGAGGTCAA | 1130 |
rs755519771 | snp | A/C | 1.65233e-05 | 0.00287426 | intron-variant | LYST | GRCh38.p7 | 1:235770317 | AGAGATAAACACACA[A/C]CAATAAGCACATACT | 1130 |
rs755521777 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235803923 | CAGATGGCAACTAAA[-/G]GTAAAATAAACATAA | 1130 |
rs755528077 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235777672 | AAATATTGGGAACTC[-/TG]TGGGTCAGGTCAATT | 1130 |
rs755530218 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874139 | TACATAAAAAGATTC[G/T]GAATATTTACAGTTT | 1130 |
rs755538881 | snp | A/G | 1.64814e-05 | 0.00287061 | intron-variant | LYST | GRCh38.p7 | 1:235693506 | AGGAGAAGGAGAAAG[A/G]AAAGTATCAGATTGT | 1130 |
rs755541761 | snp | C/T | 1.66955e-05 | 0.0028892 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752119 | GAATTGTAACTGCTA[C/T]GAAAAGTTGCTGTAT | 1130 |
rs755543845 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817274 | TTATACAACGCTGGT[A/G]GGAACGTAAGTTAGT | 1130 |
rs755547580 | snp | A/T | 3.31559e-05 | 0.00407147 | missense | LYST | GRCh38.p7 | 1:235664586 | CAACGAGATCCCCGT[A/T]CACCGTCCAGAGTCT | 1130 |
rs755560244 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844871 | ATTTAAGCAAGAAAA[-/T]TATCTGTTAATCTAA | 1130 |
rs755561019 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235815815 | GGAGAAACATTCCAC[A/G]TTCATGAATAGAAAG | 1130 |
rs755565044 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674120 | AGCCCTCCAGAGCTA[C/T]TTGGCCTCCAAGTAA | 1130 |
rs755566528 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235761479 | AGATAGAAAAGTACT[A/G]TAGGCTTAAAGACTT | 1130 |
rs755577915 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704698 | TTTCTCCCATTCTGT[A/G]GGTTGTCTGTTTACT | 1130 |
rs755582880 | snp | C/T | 3.31422e-05 | 0.00407063 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741419 | CAAAGCTGAGATACT[C/T]ACTTGTAGGGATGGG | 1130 |
rs755584683 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235737218 | GCAGGATTGTTATTA[C/G]TGATCATGTTGATCA | 1130 |
rs755594594 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235705914 | CTCCTCCCTCAGTCT[A/C]CCAAGTAGCTGGGAT | 1130 |
rs755646331 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845294 | TAGAGAGCCAAGCCT[A/G]GTGAATTACAGGGGT | 1130 |
rs755653941 | snp | A/G | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662204 | CTAAGGATAGTCAAT[A/G]TCTAGCGTTACAGAT | 1130 |
rs755654169 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235839625 | ACGGAGAACCCCCCC[C/G]ACCACGCCCCATCTC | 1130 |
rs755680605 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674878 | ATAGAAAGGACTCAT[A/G]ACATCAATCTTTATC | 1130 |
rs755699669 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842939 | TTATCTTCTTGACAC[A/T]GAGAACTACTACACC | 1130 |
rs755699804 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810194 | CTGTTCTTTGGTTGC[C/T]AAGCGGTCAAGTTTA | 1130 |
rs755706138 | snp | A/G | 1.66394e-05 | 0.00288434 | synonymous-codon | LYST | GRCh38.p7 | 1:235664484 | CAATTCCATTTTCTA[A/G]TCCCCCAGCGATTAC | 1130 |
rs755714714 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235871577 | ACATAGGAAAATAAC[A/T]ATACTAATAGCATGT | 1130 |
rs755724011 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235694915 | GGATCTATTAAAATT[A/G]AATCTAAAATTGATT | 1130 |
rs755742060 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853773 | ATAAAGGAAACTCAG[A/G]CATAGGGCAGCCAGG | 1130 |
rs755742104 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809639 | GGCTCTATGACGATA[C/G]TTTGAAAACACAAAA | 1130 |
rs755743883 | in-del | -/ACACAC | | | intron-variant | LYST | GRCh38.p7 | 1:235666230 | AGTATGTACATACAC[-/ACACAC]ACACACACACACACA | 1130 |
rs755759017 | snp | A/G | 0.00793672 | 0.0624929 | intron-variant | LYST | GRCh38.p7 | 1:235731018 | TATATGTTGAGTCAA[A/G]AAGCCACTATTACCT | 1130 |
rs755767563 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235745252 | AACATGATTTATAGT[A/G]CTTTGGAGTGTATTT | 1130 |
rs755770613 | snp | A/C/G | 0.000165817 | 0.00910399 | intron-variant | LYST | GRCh38.p7 | 1:235664100 | CAAACTAAAATTACT[A/C/G]TCCCTAAAAAGCCCT | 1130 |
rs755781095 | snp | C/T | 8.25566e-05 | 0.00642429 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730868 | GATTCACTTGCAGCT[C/T]TGTCTTTGACAGTAG | 1130 |
rs755794036 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235787448 | ACATACATATAGTAA[C/T]TATAATTCTAAATAA | 1130 |
rs755805102 | snp | A/C | 3.31323e-05 | 0.00407002 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762784 | AGGGCTCATAAGGGA[A/C]CTTCCTCCACTGCTG | 1130 |
rs755805539 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755576 | CTGGTTGGCTAGCAA[A/G]GAAAATCCACGATTC | 1130 |
rs755822869 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235666921 | TCGCTGTAACCCATA[A/G]CTACCACTACTGCAT | 1130 |
rs755828025 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235804270 | AGTAAATTTCCAGAT[C/T]AGATAAGGAAAAGCT | 1130 |
rs755850962 | in-del | -/A | 3.42059e-05 | 0.00413543 | intron-variant | LYST | GRCh38.p7 | 1:235766288 | TATTCCTGAAAAAAT[-/A]AAAAAAACTCTCTTT | 1130 |
rs755869174 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235800199 | TGATCCGCCTGCCAC[C/T]TCAGCCTCCCAAAGT | 1130 |
rs755878026 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823862 | ACTGTTTTGTCATCA[C/T]TTATTTACCTATCTC | 1130 |
rs755893037 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769632 | TTGGTTGGTATTAGA[A/T]GATATCAATAAAGGC | 1130 |
rs755896195 | snp | A/G | 3.29897e-05 | 0.00406125 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800997 | TAATTCCAGCATACA[A/G]ATCTCAGGATAAATT | 1130 |
rs755897973 | snp | C/G | 3.3661e-05 | 0.00410236 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762676 | ATCTAAGAATATTCA[C/G]AACTAAAATGAGAAG | 1130 |
rs755900129 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682873 | AATTCACTGAGTACA[C/G]ATTAGTGAGTTACTT | 1130 |
rs755905436 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235770425 | AAAGATTACATGTCT[C/G]CAAAAAGCCAATGTT | 1130 |
rs755905826 | snp | C/G | 1.65798e-05 | 0.00287917 | intron-variant | LYST | GRCh38.p7 | 1:235770118 | AGTATTATTAAACAA[C/G]TGTGGAATATATTTC | 1130 |
rs755907385 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878209 | TCCCTGGAGCAGGTG[A/G]GCTCGGCCTTCAGCT | 1130 |
rs755912639 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806221 | AACACTGAACTCAAC[A/G]TGTAGATCCAACGAC | 1130 |
rs755941997 | in-del | -/TTTA | | | intron-variant | LYST | GRCh38.p7 | 1:235754603 | TCATCTGATGCAGCT[-/TTTA]TTTGTTTCTAGTTTC | 1130 |
rs755963517 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant | LYST | GRCh38.p7 | 1:235687064 | TTTGAAAAAGGACCA[A/G]TCAAAGATTATCATG | 1130 |
rs755967766 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235825107 | AAAAAAGAAAAATCA[C/T]ATGATAGTTTCAACA | 1130 |
rs755983009 | in-del | -/TT | | | intron-variant | LYST | GRCh38.p7 | 1:235689847 | AGAATTTTAAACAAC[-/TT]TATTCAAGCTTTGGA | 1130 |
rs755995584 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235755836 | CTGTGGAATGCTAAT[A/G]ATGACTCCATCTTGG | 1130 |
rs755998933 | in-del | -/A | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739609 | AAACCTTGAACAGTG[-/A]AAAAAAAAAATAGAA | 1130 |
rs756035069 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820531 | CGTGCCACCACACCT[A/G]GTTGATTTTTGTATT | 1130 |
rs756044889 | snp | C/T | 4.95749e-05 | 0.00497845 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809476 | CCATTTGAAGAACTG[C/T]TGTTTCAAATAAATT | 1130 |
rs756047217 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702783 | CTGTTCTCGGGTCTC[C/T]CTGAAAGCAAACTGC | 1130 |
rs756058123 | snp | A/T | 1.83704e-05 | 0.00303065 | intron-variant | LYST | GRCh38.p7 | 1:235751994 | CCAAATTCATAAAAA[A/T]TAAATCTTACTTTGT | 1130 |
rs756067645 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715790 | GAAGTAGAAATGCAA[C/T]AGAAATGTAAAAACT | 1130 |
rs756069342 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700657 | GAAGCAGTATGGTGT[C/T]GAAAGTTTCACCGTG | 1130 |
rs756089583 | snp | A/G | 1.66302e-05 | 0.00288355 | intron-variant | LYST | GRCh38.p7 | 1:235801107 | CTACCCCTGAAAAGA[A/G]AAAAGCGAAAGATTA | 1130 |
rs756097379 | snp | A/G | 1.79033e-05 | 0.00299188 | intron-variant | LYST | GRCh38.p7 | 1:235812967 | ATAAAGGGAAAAAGC[A/G]TACCTGTTGCCTTTT | 1130 |
rs756121330 | snp | A/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738880 | CTTGCATCTTGGGAG[A/G]GAATGGAATCTCAGA | 1130 |
rs756124531 | snp | C/T | 1.65097e-05 | 0.00287308 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810073 | GAGAATTGTTCATGT[C/T]ACTGATAACAGACAA | 1130 |
rs756128301 | snp | A/G | 3.44483e-05 | 0.00415006 | intron-variant | LYST | GRCh38.p7 | 1:235788687 | ATTCATGGGAGGCTG[A/G]GGATAATCAATACCG | 1130 |
rs756132443 | snp | A/G | 0.000132435 | 0.00813634 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759022 | ATAACCAAGAGAATA[A/G]GCAAAGTTTTCCCAA | 1130 |
rs756133675 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859434 | ACCAAAAGTATTTGA[A/G]AGAATATATTTACTG | 1130 |
rs756139684 | snp | C/T | 9.90001e-05 | 0.00703493 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753190 | GAGTATGTTGTCATA[C/T]AGAGAGGTCTCTATT | 1130 |
rs756154838 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757454 | CCAAACAGTCTTCAG[C/T]TACACTAAAACAGAG | 1130 |
rs756157835 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235784594 | TGGCATGAGTTTGGG[-/A]AAAGTCACTCTAGGT | 1130 |
rs756161842 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235835625 | CACCAGCACAGTCAC[-/AT]GTGTCCTCCTTGAGT | 1130 |
rs756179185 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874416 | TATGGCAACATTGTG[C/T]GTAGGATTCTCTGGA | 1130 |
rs756179193 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797693 | TAAAACTTACGGGGA[A/G]CATTCCATAATATTG | 1130 |
rs756198255 | snp | C/G | 1.66818e-05 | 0.00288802 | synonymous-codon | LYST | GRCh38.p7 | 1:235709253 | ATTACGCGCCCAAGG[C/G]GGAAGGTTGACGTGA | 1130 |
rs756200789 | snp | A/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806193 | ACCACCAAGCCTATA[A/T]AACTGTTTCTGGAAC | 1130 |
rs756201918 | snp | C/G | 0.000446757 | 0.0149392 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791900 | TGTGCCAAGATGAAA[C/G]CAGCCGATGGGGAAA | 1130 |
rs756209243 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740328 | TATGAGTTTTGACAA[C/T]TGCATACATCCATTT | 1130 |
rs756209843 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689559 | TGTGCAGGATGATTA[C/T]GTTCTGGAGATCTAA | 1130 |
rs756217947 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872785 | GCCGGGTGTGGTGGT[A/G]CATGCCTGTAGTCCC | 1130 |
rs756218861 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235834082 | TAGGATGAAAGGTAT[C/T]TGAGGATACATAAGA | 1130 |
rs756226516 | snp | C/G | 4.94743e-05 | 0.0049734 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804598 | GGCTTTGCTAGTTGT[C/G]TTTCAATCACCTTTG | 1130 |
rs756240791 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235723109 | AGAGAAGAACAAGAG[G/T]CTTGGATAATCTCAA | 1130 |
rs756249440 | snp | C/G | 3.32265e-05 | 0.0040758 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808879 | CTTCTAATTGGGCTA[C/G]TTGGTCAGAGTCAAC | 1130 |
rs756256879 | snp | A/G | 1.65247e-05 | 0.00287438 | intron-variant | LYST | GRCh38.p7 | 1:235728183 | TATGTGCACACTACC[A/G]TTCATGGTTTAATGC | 1130 |
rs756271070 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791832 | AACACTGAAACCTTC[C/T]GATAGGTGTGGCCAG | 1130 |
rs756281462 | snp | A/T | 1.66029e-05 | 0.00288117 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809913 | TCCAAGTTGTCGCTC[A/T]GACTGCAGCAGTCCC | 1130 |
rs756281877 | snp | A/G | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746362 | ATCCTGTTGACTGCT[A/G]AAACAGTGAGCCTCT | 1130 |
rs756295943 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676215 | TATTCTATACTATTG[C/T]TCTCTGTCTGAACCT | 1130 |
rs756298762 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235724557 | TTTCTTACCTAAAGT[A/C]CAGAGTTTATATTCA | 1130 |
rs756306622 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819540 | GTGGGAAGTTCCCAA[C/T]GTGCCATATTAGACA | 1130 |
rs756307766 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235871823 | GTCTGGGACAAGATC[C/G]CTTTTCCGGTGACAG | 1130 |
rs756313622 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235781616 | TCCAGTATAAAAAAA[C/T]GCTAAGTTAATATGA | 1130 |
rs756314656 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235677326 | GATTGTATGACTTCA[A/G]TAAAATATAATAGGT | 1130 |
rs756322993 | in-del | -/TTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235695630 | TTTACAGTACTCTAA[-/TTTT]TTTTTTTTTTTTTTT | 1130 |
rs756335976 | snp | A/G | 3.29674e-05 | 0.00405988 | intron-variant | LYST | GRCh38.p7 | 1:235755456 | AGATTCCCAATTATA[A/G]TGGAGGGAAGAACAC | 1130 |
rs756346865 | snp | C/G/T | 0.000132402 | 0.00813553 | intron-variant | LYST | GRCh38.p7 | 1:235733493 | TTTTAACTGACCTCC[C/G/T]GCAGCTTACCTATCA | 1130 |
rs756352164 | snp | A/G | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660751 | AAAAGTTAGCCGGGC[A/G]TCGTGGCACACTCCT | 1130 |
rs756357661 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708911 | CACCTCTGAAAAAGA[C/T]AGTATCTTGTTTTTA | 1130 |
rs756365183 | snp | A/G | 1.66729e-05 | 0.00288724 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744141 | TCTCAAAATGTCAAT[A/G]ATGTCTGAATTAAAT | 1130 |
rs756381548 | snp | C/T | 0.000104292 | 0.00722045 | missense | LYST | GRCh38.p7 | 1:235712062 | ATTGCTATACCTTCA[C/T]GGTTAACTAGGAACT | 1130 |
rs756383366 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235726664 | GATTTGAAAAAAAAA[-/T]TTTTCCTCTTTATTT | 1130 |
rs756389940 | in-del | -/A | 1.66574e-05 | 0.0028859 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808436 | CCCGCCCCCGCCGCC[-/A]ACCCACACACATACA | 1130 |
rs756397723 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235783038 | AAGCAGGGAGGACTT[C/T]ATCAACTAGTGAAAC | 1130 |
rs756401592 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765093 | CACCTCACTTCTATG[C/T]GGACAGCTCCTTATA | 1130 |
rs756437751 | snp | C/T | 1.6513e-05 | 0.00287336 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806521 | CCAGCATAAAATTTG[C/T]TGAGACTCTGAGGAG | 1130 |
rs756441216 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715636 | TAACTTTGAGCACTC[C/T]ACCTCCTAACTAATG | 1130 |
rs756441252 | snp | C/T | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773892 | GTTCCTCTAACAGCT[C/T]AACATCTTGGATTAT | 1130 |
rs756442535 | snp | C/T | 2.08971e-05 | 0.00323236 | intron-variant | LYST | GRCh38.p7 | 1:235780823 | ATAAATATACCTAAA[C/T]ACATTTACTATAAAA | 1130 |
rs756443598 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235703398 | AAACCAAAAGAGCAG[A/C]AATGAAAATTCAAAG | 1130 |
rs756444894 | in-del | -/AACC | | | intron-variant | LYST | GRCh38.p7 | 1:235692339 | CTTCATCTCATAACA[-/AACC]AACCAACCAACCAAC | 1130 |
rs756449814 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697949 | TGAAGACTCTAGAGA[A/G]ATACCCATTTGGCTG | 1130 |
rs756467690 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820530 | ACGTGCCACCACACC[C/T]GGTTGATTTTTGTAT | 1130 |
rs756491810 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235766492 | AACACAGATGGCAAC[C/T]TAATTCTAGCCCATG | 1130 |
rs756493484 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882987 | ATACTCTTCCCTGCG[G/T]TTTCTCTACAGTCCT | 1130 |
rs756511851 | snp | C/T | 3.2981e-05 | 0.00406071 | missense, downstream-variant-500B, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751224 | CCAGCAATGCTTTTC[C/T]GCTTTTGAACTACTG | 1130 |
rs756525512 | snp | A/T | 1.64814e-05 | 0.00287061 | intron-variant | LYST | GRCh38.p7 | 1:235804492 | AACACAACTATATGT[A/T]GTTATTCATACCTTC | 1130 |
rs756527704 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807319 | GAACAGTCAATGGTA[C/T]AAATATTATAAAAGT | 1130 |
rs756527768 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809197 | GCTCAGGATAATAAA[A/C]ATCTCCATCTGCAGT | 1130 |
rs756527927 | snp | C/T | 0.000148465 | 0.00861454 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791729 | TGCTATCTGGTAAAA[C/T]TAATGATTTGTTTCT | 1130 |
rs756537032 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235747989 | GACTGATAAAATAGC[A/G]ACTGGTACATGGTTG | 1130 |
rs756544915 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689950 | AATAAATTAGTGAAT[C/T]GGAAAGCATCTTTAA | 1130 |
rs756551414 | snp | C/T | 3.29696e-05 | 0.00406001 | missense | LYST | GRCh38.p7 | 1:235697097 | CCTTGTTCCTTGCTA[C/T]ATGTCATCAGAAGAC | 1130 |
rs756559518 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235863799 | AAACAAAGTCACTTG[C/T]GTTTACTACTAATAA | 1130 |
rs756566909 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806637 | ATCTGGAACTGAGGC[A/G]TCTTTCTGTTGCTCC | 1130 |
rs756567752 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746965 | AATTTCATAAAGTAG[-/T]TTTAAAAACTGTGTA | 1130 |
rs756582599 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862451 | GCCCTATAGTGTATA[C/T]AGGATTCAGTACTAT | 1130 |
rs756590795 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235877587 | AATTTTGTATTTTTA[C/G]TAGACATGAGGTTTC | 1130 |
rs756591389 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778515 | GAGTAGCTGGAATTA[C/T]AGGTGCATGCCACCA | 1130 |
rs756604740 | in-del | -/ATTT | | | intron-variant | LYST | GRCh38.p7 | 1:235856940 | ACACAGGATATACTG[-/ATTT]TTTTTTTTTTTTTTT | 1130 |
rs756613015 | snp | A/G | 1.65097e-05 | 0.00287308 | synonymous-codon | LYST | GRCh38.p7 | 1:235697222 | TACTGGAGCACTGGG[A/G]GAACCCACGTATTCC | 1130 |
rs756622866 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235734876 | TGTTAGATGTAATAA[A/T]GTTATGTTACATAGG | 1130 |
rs756645604 | snp | A/G | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773987 | CAGCATCCTTCAAGA[A/G]GGGTCTATAGAAAAT | 1130 |
rs756645857 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235876747 | TGCCCAGCTCACTAC[A/G]TAAGCTAATTTGAGA | 1130 |
rs756647640 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736235 | AAAAAACTGATTTAA[A/G]GAATTGAATCTGTTA | 1130 |
rs756651685 | snp | C/G/T | 4.97017e-05 | 0.00498485 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762788 | CTCATAAGGGACCTT[C/G/T]CTCCACTGCTGGAAT | 1130 |
rs756652843 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684684 | GCAGTGGTGTGGTCA[C/T]GGCTTACTGCTGTGA | 1130 |
rs756657197 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235674576 | AAATGTAGACTGGAT[-/A]AATTACGTTTATTAT | 1130 |
rs756673506 | snp | C/T | 8.18147e-05 | 0.00639536 | intron-variant | LYST | GRCh38.p7 | 1:235734686 | GTAATAATTTTTTAG[C/T]CATTTAGAATTTTAA | 1130 |
rs756678386 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon | LYST | GRCh38.p7 | 1:235663024 | ACACCAGGCAATCAC[A/G]GTCCCATCACTGTTT | 1130 |
rs756682993 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235717703 | TAACCACATGTTGAT[A/G]CATCTTTTTTTTTTT | 1130 |
rs756700383 | in-del | -/T | | | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235808184 | GTATCCTCTTCTCTA[-/T]AAACAGCTCAGTAAA | 1130 |
rs756716492 | snp | A/G | 1.64822e-05 | 0.00287068 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830288 | CATGGACAAGGTACT[A/G]TCCAAGGGTTGCCAT | 1130 |
rs756735142 | snp | A/T | 1.65007e-05 | 0.00287229 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808521 | TGAGGCAAGCACTGG[A/T]TATGATGGCTACATA | 1130 |
rs756757873 | snp | A/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759408 | CGGAACTCCCCAAAG[A/T]ATTTTGTTTCTTTGA | 1130 |
rs756782154 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235857048 | CCTCCTAGGTTCAAG[C/T]GATTCTCATGCCTCA | 1130 |
rs756782688 | snp | C/T | 1.6902e-05 | 0.00290701 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777065 | CAGTGATTCTTACCC[C/T]GGCAAAGAGAAAAAC | 1130 |
rs756788509 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235708832 | ACCTGAGCTGGAAGG[A/G]TGACTATATGCTGAA | 1130 |
rs756790912 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235849070 | CATAACCAAAAAGAG[-/A]AAACTACAGAACGAT | 1130 |
rs756800403 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235829216 | TCTCAAAAAAAACCA[C/T]AAACCTACAAATGTC | 1130 |
rs756803088 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731052 | GATTTCTGTCTATCC[C/T]TAAGGAGATACTTAT | 1130 |
rs756813987 | snp | C/G | 1.66763e-05 | 0.00288753 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762701 | GAGAAGGTCATACTT[C/G]CATTATTGCTATTTT | 1130 |
rs756826612 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673496 | CCACCAAAAATCAAG[G/T]TTAGACATCCTCAGA | 1130 |
rs756826964 | snp | A/C | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806014 | TCACTTTTTATAGCC[A/C]AAGATAATAAATCTT | 1130 |
rs756830243 | in-del | -/A | 1.6516e-05 | 0.00287362 | intron-variant | LYST | GRCh38.p7 | 1:235664064 | CATAACCTAGAGGGG[-/A]AAAAAAATCATCTAA | 1130 |
rs756833811 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235818736 | CTAATAGCATTCTAA[C/T]GGAGCTTGCAGAAAC | 1130 |
rs756854305 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235704593 | CCTTTGCACACTTTT[A/T]AATGAGGTTGTTTTT | 1130 |
rs756867102 | snp | A/G | 1.64936e-05 | 0.00287168 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810385 | TAATTTTACGCTGTC[A/G]TCTGCTTTTTCGAAA | 1130 |
rs756876416 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235873745 | CAAATTTCTGATTAA[C/T]TTTCACCTGAAACCA | 1130 |
rs756888265 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235815397 | GACAAAAAGGGTAAC[A/G]TTTTAGACAGGCTAT | 1130 |
rs756888276 | snp | C/T | 1.64993e-05 | 0.00287218 | intron-variant | LYST | GRCh38.p7 | 1:235677052 | AATGCGCTGTTAGAG[C/T]ACCAGCCAGCCCTGT | 1130 |
rs756899169 | snp | C/G | 1.65477e-05 | 0.00287638 | intron-variant | LYST | GRCh38.p7 | 1:235716702 | AAGTACGAGTAAAAA[C/G]AAAAGCTACCTTGTA | 1130 |
rs756899727 | snp | G/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757406 | TAAGAAGAACCCCAC[G/T]TAGGAGTTCATATAA | 1130 |
rs756915263 | snp | A/T | 3.01046e-05 | 0.00387961 | intron-variant | LYST | GRCh38.p7 | 1:235757248 | ATATTTATTTTTCTG[A/T]ATTAAAATAACATAT | 1130 |
rs756922197 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235761124 | TTTAAAAAGAAAAGG[A/G]AAACTAATAAAAACA | 1130 |
rs756923995 | snp | A/C/T | 3.29599e-05 | 0.00405944 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810291 | TTATTCATTGCTATG[A/C/T]CTTTTTCATCTGAAT | 1130 |
rs756944648 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235855496 | ATAAAATTTTGGATG[C/T]TTATTCATACTGTTA | 1130 |
rs756956175 | snp | C/T | 3.52224e-05 | 0.00419642 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752007 | AATTAAATCTTACTT[C/T]GTGTCCTCTTGTTTT | 1130 |
rs756956236 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235729719 | TTTCAGAGAGGATAT[C/G]CTTTATTTTACCTAG | 1130 |
rs756963076 | snp | A/G | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661939 | TGGTATAGGTTAGTA[A/G]AAACAGAATGAAATG | 1130 |
rs756980350 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235817150 | CCAATTAGAGAAATG[A/C]AAATCAAAACCACAA | 1130 |
rs757005691 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868856 | ATGTGCTACCATGCC[C/T]GGCTAATTTTGTATT | 1130 |
rs757015092 | snp | A/C | 1.65348e-05 | 0.00287526 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793587 | CATCAAAGATACCAA[A/C]AGATCCACCAATACT | 1130 |
rs757026164 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235836857 | CTATGTTAGGTGTGA[C/T]AGGTTTCTTAGAAAT | 1130 |
rs757030172 | snp | C/G | 1.65573e-05 | 0.00287721 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788824 | GGATTTATGTACTCT[C/G]CACCTTCTGGTCTGT | 1130 |
rs757042072 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant | LYST | GRCh38.p7 | 1:235723981 | TATAGTTACAGTGGC[C/T]CATGAGCACTTAAAC | 1130 |
rs757049801 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743555 | TGACACTTATCAGTA[A/T]TCTCTACATAATTTT | 1130 |
rs757052620 | snp | C/T | 1.65097e-05 | 0.00287308 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809669 | ATCTTCCTGAACCTC[C/T]TGCAGTGTTTTCTTT | 1130 |
rs757064012 | snp | A/C | 3.30874e-05 | 0.00406726 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802950 | GATTGCTTTCACTAT[A/C]TGCTTCGTAACCTTC | 1130 |
rs757066505 | snp | A/T | 1.65302e-05 | 0.00287486 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809514 | TGATGCTGAATGAAT[A/T]CTTGAACCAAATCCA | 1130 |
rs757070479 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822146 | CAAAATGAAAAAAGG[C/T]CTCTGGGCGCCCACT | 1130 |
rs757075419 | snp | C/T | 3.30169e-05 | 0.00406293 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759097 | TGCAGATCCGTTCTG[C/T]GAAGGAAAAGCTAGC | 1130 |
rs757078750 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681437 | TCCCCGAAGCAATAA[A/G]GGGTCACTGAAGTGT | 1130 |
rs757091601 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235881103 | CTGGAACTGGGGTTC[C/G]TAACTCCAAATTTCT | 1130 |
rs757110076 | snp | C/T | 4.52458e-05 | 0.00475614 | intron-variant | LYST | GRCh38.p7 | 1:235830148 | AGGAGGCTTCAGAAA[C/T]TATGTAATCCAAAAC | 1130 |
rs757113956 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235838073 | AATGTCAGAGAATAC[A/G]AGTATAGATGTAGGA | 1130 |
rs757162379 | in-del | -/TAT | 1.65479e-05 | 0.0028764 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716754 | TTTTCTTTATACTGA[-/TAT]ACAGCTATAGGTTTA | 1130 |
rs757169298 | in-del | -/AACT | | | intron-variant | LYST | GRCh38.p7 | 1:235793383 | GAAATTGCCTATACC[-/AACT]GTCACATCAAAAGAA | 1130 |
rs757176264 | snp | A/G | 8.42822e-05 | 0.00649107 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808431 | ACAACCCCCGCCCCC[A/G]CCGCCACCCACACAC | 1130 |
rs757183259 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769500 | TACTGATCTCATGGA[A/G]TATCTGTACTTATCT | 1130 |
rs757192132 | snp | C/G | 1.67301e-05 | 0.00289219 | intron-variant | LYST | GRCh38.p7 | 1:235709046 | CCTTAAAATATTCAG[C/G]TTCTATCTTATATAA | 1130 |
rs757194359 | snp | C/T | 3.32441e-05 | 0.00407688 | missense | LYST | GRCh38.p7 | 1:235664616 | TGAGGTCACTGCCTC[C/T]GCCAGCTAAAACACC | 1130 |
rs757203113 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758348 | CCTAGGCAATGTCTG[C/T]CATAACATGGAGGAC | 1130 |
rs757208948 | snp | C/T | 3.31768e-05 | 0.00407275 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741568 | GCATTCGGAAGGTCT[C/T]CTTACAAGACCACAG | 1130 |
rs757222354 | snp | A/G/T | 3.32133e-05 | 0.00407502 | synonymous-codon, stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775041 | ATGAGAGTATAACTC[A/G/T]CAGTGCTAATGCTTG | 1130 |
rs757224472 | snp | C/G | 3.35531e-05 | 0.00409578 | intron-variant | LYST | GRCh38.p7 | 1:235788890 | TAAAATGGTTCGTAA[C/G]AACTGAGTAGAAAAG | 1130 |
rs757226249 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789170 | GCTTCTTTTATCAAC[A/T]ATGACTTCACTGACC | 1130 |
rs757227472 | snp | A/T | 1.67441e-05 | 0.0028934 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752135 | GAAAAGTTGCTGTAT[A/T]TCACAAGCAAGCAAT | 1130 |
rs757231255 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235729791 | CATGAGGTATCTTGT[C/T]GAAACCCACATGAAA | 1130 |
rs757235852 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235823662 | CTTCGCTGTAACTTC[A/C]CTAAACTACTTGTAG | 1130 |
rs757239793 | snp | G/T | 4.9467e-05 | 0.00497303 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724100 | AGCATTATCTCTCAA[G/T]TGCCACCAACGCTTG | 1130 |
rs757251974 | in-del | -/TAA | | | intron-variant | LYST | GRCh38.p7 | 1:235689052 | CAACAACAACAATAA[-/TAA]TATCCTAGCTGAATT | 1130 |
rs757271317 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753797 | GTCCTCTTTTCTTCT[C/T]AAGGCTATTGTGAGA | 1130 |
rs757271507 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770222 | TCAATAACTGCTTAA[C/T]ATTAAACATCTGCTG | 1130 |
rs757275515 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746379 | AACAGTGAGCCTCTG[C/T]AGTCTCTGCGCAAGT | 1130 |
rs757284196 | snp | C/T | 4.94222e-05 | 0.00497078 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702894 | CAGCTGACGGGGAGT[C/T]TGCCCGTAGGTTTTT | 1130 |
rs757286272 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235670039 | CTTCAAAGCTCCCTT[A/G]GTCTTTCTTGCTCTG | 1130 |
rs757291578 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755542 | CTAACAATTCTTGAG[C/T]TCCTCGATGAAGATA | 1130 |
rs757303313 | snp | A/C | 1.69856e-05 | 0.00291419 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780970 | GTAGTCATTGACTGG[A/C]TTGCCATACTTACAT | 1130 |
rs757309128 | in-del | -/ATA | | | intron-variant | LYST | GRCh38.p7 | 1:235829698 | AACTCTGTTAATTTT[-/ATA]ATAAGAAAACAGCAA | 1130 |
rs757310129 | snp | A/T | 9.9557e-05 | 0.00705468 | intron-variant | LYST | GRCh38.p7 | 1:235780840 | CATTTACTATAAAAT[A/T]AAAATTTATAAAATT | 1130 |
rs757321389 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235810830 | ACATTACTTCAAAGG[A/T]TACAAACTGATTTTT | 1130 |
rs757331327 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | LYST | GRCh38.p7 | 1:235686899 | CATAAAGGCTTTCTT[C/T]CCCTCATTGACAAAG | 1130 |
rs757331695 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670857 | AGGTTGAACCCCATA[C/T]AGTCAGGAAACTCAG | 1130 |
rs757360584 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235755246 | TACAAAAAACTAGCC[A/G]GGCATGGTGGTACGT | 1130 |
rs757379494 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860514 | ATTCATCCCTCCTTC[A/T]CTCCACCACTAATCT | 1130 |
rs757381951 | snp | A/C | 1.65457e-05 | 0.00287621 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809011 | GAAAATTTTTCAGTG[A/C]TGGCAATTTAAAAGC | 1130 |
rs757388781 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791993 | CCTTACTGTTTAAAA[C/T]CCCAGGATACTTTTG | 1130 |
rs757404646 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | LYST | GRCh38.p7 | 1:235733808 | CCTAAAATACATGCC[C/T]TTGGAACATATAAAA | 1130 |
rs757411778 | snp | A/T | 1.7294e-05 | 0.00294053 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235812979 | AGCATACCTGTTGCC[A/T]TTTCTTCTTGGACAG | 1130 |
rs757425149 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235873035 | CACGGCCTATCTTGA[A/C]GGAGAAAGAGAAGCA | 1130 |
rs757456237 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801034 | CCTTGAGTGAGGTTT[C/T]CGAGTAAGTCATTTG | 1130 |
rs757459182 | snp | G/T | 1.6577e-05 | 0.00287893 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715176 | TGACCCAACATGACT[G/T]TTTAGGCAGTTATTA | 1130 |
rs757461533 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235796138 | TCAAGATAACAATTA[C/G]AATACAAAAAAAGAG | 1130 |
rs757467358 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235859557 | CAACAAAGGAAATAA[A/C]ACAGCTAATTCCACC | 1130 |
rs757469831 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235675805 | GGCAGCCTCCAAATT[C/T]GCAAACTTCTAGTGT | 1130 |
rs757471831 | snp | C/T | 4.98716e-05 | 0.00499333 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808905 | TCAACAGTACAAATA[C/T]TACAAGCTGCTTTTT | 1130 |
rs757473150 | snp | A/G | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746456 | GCATCATCACATGAA[A/G]CTCATCATTTGCCAC | 1130 |
rs757490541 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722768 | GGATTACAGGCATGA[A/G]CCACTGTGCCCGGCC | 1130 |
rs757494655 | snp | A/T | 1.72838e-05 | 0.00293966 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774927 | CCTTCAAAATGTAAA[A/T]CCCAACAATGCATTT | 1130 |
rs757502820 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715311 | GGCTGCACGGGAGGC[A/G]TGGGGTCATCTTCTC | 1130 |
rs757503541 | snp | A/G | 8.25948e-05 | 0.00642577 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733681 | ATTTTGAATCCAGAC[A/G]CTGAAAGAGACTAAA | 1130 |
rs757504813 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763228 | ATCCCCTTCAGTGTC[C/T]AATATTTGTAAAAAC | 1130 |
rs757527428 | snp | A/C | 1.65042e-05 | 0.0028726 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770257 | TGATCTGCTCTGATG[A/C]GGACTTCTAGAGCTG | 1130 |
rs757549816 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797513 | TGCCAAAACCATTCA[A/G]TGGGGGAGGGACAGT | 1130 |
rs757560834 | snp | A/G | 4.98749e-05 | 0.00499349 | synonymous-codon | LYST | GRCh38.p7 | 1:235664617 | GAGGTCACTGCCTCC[A/G]CCAGCTAAAACACCC | 1130 |
rs757590207 | snp | C/T | 1.66241e-05 | 0.00288302 | intron-variant | LYST | GRCh38.p7 | 1:235664104 | CTAAAATTACTCTCC[C/T]TAAAAAGCCCTCTAT | 1130 |
rs757591957 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872005 | TAATCAGAGTTTTAC[A/G]TAACATGGGGCCAAG | 1130 |
rs757597856 | snp | A/C | 2.31822e-05 | 0.00340449 | intron-variant | LYST | GRCh38.p7 | 1:235734694 | TTTTTAGTCATTTAG[A/C]ATTTTAATTCTTACA | 1130 |
rs757598042 | in-del | -/TTACA | | | intron-variant | LYST | GRCh38.p7 | 1:235764900 | TTCTTGCTTTCTTTC[-/TTACA]TTACATTTCCCTGGT | 1130 |
rs757612404 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235833986 | AACACTAGAATCTAG[A/G]AGGCAGCGGAATATC | 1130 |
rs757615539 | snp | C/T | 1.65641e-05 | 0.00287781 | intron-variant | LYST | GRCh38.p7 | 1:235770126 | TAAACAACTGTGGAA[C/T]ATATTTCCAAAAGTA | 1130 |
rs757637066 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806655 | TTTCTGTTGCTCCCC[C/T]AGGCTGATTATCAGA | 1130 |
rs757656987 | snp | A/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724180 | ACTCTCCCTGAAGGC[A/T]CTAAGACAAAGAAAT | 1130 |
rs757659375 | snp | G/T | 1.66117e-05 | 0.00288194 | intron-variant | LYST | GRCh38.p7 | 1:235774003 | GGGTCTATAGAAAAT[G/T]AGCATTAATATAAGA | 1130 |
rs757659380 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831122 | TAGTTTCATCTCTGG[A/G]CTAAAAGTAATTTTG | 1130 |
rs757680153 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819320 | TTTATCCTCTCTGGT[C/T]CCAAAGAAACCACAT | 1130 |
rs757681668 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764846 | TTGTACAACCAGTTT[C/T]CCAATGTAAATTTAT | 1130 |
rs757686383 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719903 | TAATGGCTGGCTGGG[C/T]GTAGTGGCTCATGCC | 1130 |
rs757702125 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235852484 | CCGGACCTTTTTCCC[A/G]GGGAAGTCTCACAAT | 1130 |
rs757708194 | snp | G/T | 1.65143e-05 | 0.00287348 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830352 | CACCCTCTGGACCAC[G/T]GCATTGCAAAGCCGG | 1130 |
rs757720614 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235665931 | TCATACTGATAAAGC[A/G]GTTAGGAGGCACGAT | 1130 |
rs757722584 | in-del | -/A | 5.25366e-05 | 0.00512499 | intron-variant | LYST | GRCh38.p7 | 1:235773819 | CACAATAAAAAATGG[-/A]AAAAAAAGTACATAT | 1130 |
rs757725392 | snp | G/T | 1.64808e-05 | 0.00287057 | intron-variant | LYST | GRCh38.p7 | 1:235755461 | CCCAATTATAGTGGA[G/T]GGAAGAACACACTTA | 1130 |
rs757732333 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667550 | TATAGTTGTCCCTAG[A/G]TATCTGAGAGGGATT | 1130 |
rs757739442 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235716892 | AAATGCTCCACCCTT[A/G]TTTCTCTGCTTAAAC | 1130 |
rs757766276 | snp | A/C/T | 8.24632e-05 | 0.00642072 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806308 | CTCTCGAGAGATATA[A/C/T]ATGGCAGCATATGAC | 1130 |
rs757771673 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746892 | TTCCAAAATCAAGTT[C/T]TAATGCACATAATTT | 1130 |
rs757772723 | snp | A/G | 1.65004e-05 | 0.00287227 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810085 | TGTTACTGATAACAG[A/G]CAAGGCAGCTGGCTC | 1130 |
rs757777514 | snp | G/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662110 | CTGAAGGCTTTCTAT[G/T]GCAAATTGGTACAGA | 1130 |
rs757786740 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235696702 | TTTTCAAGGCTATCT[C/T]GACATCCTTGTTGTG | 1130 |
rs757789045 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708677 | AGACAACATTTCACA[C/T]GTGTCATTATGACTC | 1130 |
rs757803872 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864346 | CCAACTCCCACCCTT[C/T]TCCCCACCAAACCTA | 1130 |
rs757812223 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235864168 | TCTCATGCTGTATTC[A/G]GAGTTGAGCCCAGTC | 1130 |
rs757826260 | snp | G/T | 1.65053e-05 | 0.0028727 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809214 | TCTCCATCTGCAGTC[G/T]CTTCAAATGGGTTTT | 1130 |
rs757827141 | in-del | -/CCCA | | | intron-variant | LYST | GRCh38.p7 | 1:235812250 | GCTCATGCCTGTAAT[-/CCCA]CCCAGCACTTTGGGA | 1130 |
rs757828568 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684548 | ATTCATTTTAAGCCT[C/T]TGGGAATCAAAAGGT | 1130 |
rs757831896 | snp | A/C | 0.000363991 | 0.0134857 | intron-variant | LYST | GRCh38.p7 | 1:235730825 | TTCATGAAAGAGTGA[A/C]GGTCTATTGATTCAA | 1130 |
rs757852938 | snp | C/T | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806096 | TTACACTTGTATCTC[C/T]CTCCTTTTTTCCTTG | 1130 |
rs757860048 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761736 | GCTGGATAGGGAAAG[C/T]GAGACAAGGGGAACT | 1130 |
rs757860752 | snp | C/T | 0.000249006 | 0.0111553 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809917 | AGTTGTCGCTCAGAC[C/T]GCAGCAGTCCCCAAA | 1130 |
rs757866901 | in-del | -/G | 1.64819e-05 | 0.00287066 | intron-variant | LYST | GRCh38.p7 | 1:235755460 | CCCAATTATAGTGGA[-/G]GGGAAGAACACACTT | 1130 |
rs757871162 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853967 | AGATATTGTAGCTAT[-/AG]AGAGAGAGACGGCAT | 1130 |
rs757883513 | snp | C/T | 1.6574e-05 | 0.00287867 | intron-variant | LYST | GRCh38.p7 | 1:235731224 | GTGACCATCCAGGAC[C/T]TGTAGCTATAAAAAA | 1130 |
rs757885542 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235772433 | TTTTTGCAAAAATCA[C/T]CAGTACCTACTAGAA | 1130 |
rs757886502 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235849777 | TTTACAATAGCTCCA[-/AA]AAAAAAAAAAAAAAA | 1130 |
rs757888069 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235797398 | AAATCATGTTGACAA[C/T]ATGTACCCTTGATAT | 1130 |
rs757904572 | snp | C/T | 1.66971e-05 | 0.00288934 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810505 | TTTCTTTGGTCAGGA[C/T]TATATCTGCTGAGAG | 1130 |
rs757912379 | snp | G/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810391 | TACGCTGTCGTCTGC[G/T]TTTTCGAAAAACATT | 1130 |
rs757918402 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672410 | GACTGAGAAGGACCC[A/T]CCAGTGACCTAGAAG | 1130 |
rs757927726 | snp | A/C | 1.92121e-05 | 0.0030993 | intron-variant | LYST | GRCh38.p7 | 1:235762898 | ATTTTTAAAAAGGAT[A/C]AAACGAAAATATAAC | 1130 |
rs757934089 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235877977 | ACAGGGTGTTACTAG[A/G]TTCTAGAAATCTAAC | 1130 |
rs757945250 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875559 | AGCCAGGGGGCAGCT[A/G]CATCATGCTGATGGA | 1130 |
rs757963598 | snp | C/T | 1.65348e-05 | 0.00287526 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716718 | AAAAGCTACCTTGTA[C/T]GTGTCCACATAACGA | 1130 |
rs757965999 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792852 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATCATAT | 1130 |
rs757967032 | snp | A/G | 0.000404961 | 0.0142238 | intron-variant | LYST | GRCh38.p7 | 1:235800391 | TTCACAGTTCCCTGA[A/G]GATTAAAAAAAATAC | 1130 |
rs757974517 | in-del | -/AGA | 0.000116745 | 0.00763931 | intron-variant | LYST | GRCh38.p7 | 1:235733909 | ATTTCTTTTGTTCCT[-/AGA]AGATTTAGATAATAA | 1130 |
rs757982705 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon | LYST | GRCh38.p7 | 1:235697231 | ACTGGGGGAACCCAC[A/G]TATTCCCCCCATTTC | 1130 |
rs757985092 | snp | C/T | 1.68145e-05 | 0.00289948 | intron-variant | LYST | GRCh38.p7 | 1:235793655 | AAAGCTAGTACACAA[C/T]TAGAGGAATAAATGA | 1130 |
rs757992741 | in-del | -/AAATTAAAT | 1.64866e-05 | 0.00287106 | intron-variant | LYST | GRCh38.p7 | 1:235716802 | AAAGGACAATTTTAA[-/AAATTAAAT]ATTTTGATACTGTCA | 1130 |
rs757994690 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827444 | AATCACCCCAGAGTA[C/T]TCAAGAAGTGCTCCT | 1130 |
rs758000419 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685643 | CTGAGCTCAGGAGCT[C/T]GAGACCAGTCTGACC | 1130 |
rs758004328 | snp | G/T | 1.6519e-05 | 0.00287388 | intron-variant | LYST | GRCh38.p7 | 1:235720621 | AGAAATACAACATAT[G/T]GATGGATGAACCCTA | 1130 |
rs758009178 | snp | A/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806556 | TGAATAAGCTTGCTG[A/T]TGATGAAAAGAAGTA | 1130 |
rs758009409 | in-del | -/GT | | | intron-variant | LYST | GRCh38.p7 | 1:235750533 | TACTCTGGAGATGGT[-/GT]GTGTGTGTGCATGTG | 1130 |
rs758029213 | snp | A/C/T | 8.24444e-05 | 0.00642002 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809318 | TTCACATCGTCTGTG[A/C/T]CTTTTTCTTGTACAC | 1130 |
rs758045352 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751329 | AATTCCATAGCAGCC[C/T]GGAGAACTCTAAGCT | 1130 |
rs758049109 | snp | A/C | 4.94548e-05 | 0.00497242 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751232 | GCTTTTCCGCTTTTG[A/C]ACTACTGCATGATGG | 1130 |
rs758067660 | in-del | -/AACC | | | intron-variant | LYST | GRCh38.p7 | 1:235702362 | TTGATTGTAGATGAT[-/AACC]AAGACCATGGTATGC | 1130 |
rs758070828 | snp | C/T | 3.29576e-05 | 0.00405928 | missense | LYST | GRCh38.p7 | 1:235697133 | TTCCGTGACAAACCA[C/T]AGATTGCTCTGGTGG | 1130 |
rs758084340 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814071 | AACTAAAATAACTTG[C/T]AGTTGATTATCTATG | 1130 |
rs758086501 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235842753 | ATGGTCACTAAAGTC[A/C]GTCAACAGTGGCTCT | 1130 |
rs758088188 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235815190 | TCCGTTAAACAAATA[C/T]TTCTTGATCCCCCTA | 1130 |
rs758088473 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673346 | GCAGGAACCTTCAAC[A/G]CCAAAGAGAAATAGC | 1130 |
rs758089264 | snp | A/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712477 | ATCTATCAAAGTAGA[A/T]TGAAAGTTCCACAAA | 1130 |
rs758099465 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734599 | CTAGCTCTTCTTCAG[C/T]CAATTCACCTTGGTG | 1130 |
rs758107307 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718779 | AAGGCAGAATAAATG[A/C]TGAATTCTGTTCCTT | 1130 |
rs758107516 | snp | G/T | 3.32723e-05 | 0.00407861 | intron-variant | LYST | GRCh38.p7 | 1:235757502 | AACATGACAAGAAAA[G/T]TACTTGATGATTACC | 1130 |
rs758129842 | snp | A/G | 1.66026e-05 | 0.00288115 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777090 | AAAAACAAATATGCC[A/G]GTTCCACCAATTTCG | 1130 |
rs758133195 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703518 | ATGGAGAGCAATGCA[C/T]ATTTACTTATTTCTA | 1130 |
rs758149467 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841455 | TCCCAGCATCACTGG[C/T]ACCATGTTGGTAGCT | 1130 |
rs758152228 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235857168 | GCCAGGTTGGTCTTG[A/T]ACAATAGGCATAAAC | 1130 |
rs758162960 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787261 | TCCCTTGGGGCTGCT[C/G]TAAGTAGGTGAGTAC | 1130 |
rs758173110 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852685 | GTTGATTGACAATAA[A/G]GGAAAACTGCCAGAG | 1130 |
rs758177897 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869840 | TCTTTCTACTCTCCC[A/G]TCACTACCTACATAC | 1130 |
rs758182299 | snp | C/T | 0.000131989 | 0.00812264 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808545 | CTACATACATGACTT[C/T]GAGCTGAAGTAACGC | 1130 |
rs758202528 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235835710 | TTCTAGGTGTCCAGA[A/G]CATCTGGAAGTATAG | 1130 |
rs758214258 | snp | C/T | 1.67103e-05 | 0.00289048 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741596 | CAGAATTTTAGTCCA[C/T]TGCTGCTTGGAACCA | 1130 |
rs758216210 | snp | C/T | 1.74269e-05 | 0.00295181 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753055 | TTACTTCTTTTCTAA[C/T]CCATTCAGGGCTGCT | 1130 |
rs758228881 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693087 | TTGGGAGGCCAAGGC[A/G]GGCAGATAACAAGGT | 1130 |
rs758244326 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235855694 | TTCATATATATTTTG[C/T]ATAAGGTTAAAGATT | 1130 |
rs758287853 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235742625 | GACATGGACAACGAA[C/G]CTAAAGTCCTAAGCC | 1130 |
rs758294791 | snp | G/T | 1.68352e-05 | 0.00290126 | intron-variant | LYST | GRCh38.p7 | 1:235677225 | TTTGTATATGATCAT[G/T]AAATATAATTACATT | 1130 |
rs758307405 | snp | C/T | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806036 | ATAAATCTTCCTTCA[C/T]AGTTCTCTTAGGTTG | 1130 |
rs758339215 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235710534 | CAGACAACTGACATA[C/T]GAGAGTCCCAGGGGA | 1130 |
rs758365811 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753891 | CATTGAAACTACCAT[A/T]ACAATTTAGTAAATT | 1130 |
rs758390448 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235743407 | GATTTAGAGATTGAC[A/G]TGTCATGATTTACGA | 1130 |
rs758392578 | in-del | -/CA | 3.30863e-05 | 0.00406719 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808604 | AACTCCTCTTTGGAG[-/CA]CAGGATTAAATATGT | 1130 |
rs758413196 | snp | C/G | 3.32884e-05 | 0.00407959 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744005 | TGAATCCTTCTACCA[C/G]ATATGTAAAAATTTC | 1130 |
rs758426723 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235720428 | ATACTGTAGAACAAA[A/G]AAGTGACATAACAAG | 1130 |
rs758431233 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820896 | TTTCTTTTCTAGCTG[C/T]ATAGCTGCAGCTAAA | 1130 |
rs758441925 | snp | A/C | 1.65501e-05 | 0.00287659 | intron-variant | LYST | GRCh38.p7 | 1:235770138 | GAATATATTTCCAAA[A/C]GTAAAGTTACATGAA | 1130 |
rs758452264 | in-del | -/A | 0.00572004 | 0.0531724 | intron-variant | LYST | GRCh38.p7 | 1:235775089 | TGAGTTCAACAACCT[-/A]AAAAAAAAAATGGGT | 1130 |
rs758454845 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881208 | ATTTTGCCAGAGTTT[A/T]ATTTTAGACTGCAAG | 1130 |
rs758455804 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235680003 | TCTCTCTCTCTCTCT[A/C]TAAATATCTATGTAT | 1130 |
rs758469221 | snp | C/G | 1.64931e-05 | 0.00287163 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662893 | GTGAAGTCAACAAAT[C/G]TAGTTTGGAGTTAAA | 1130 |
rs758475253 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235849100 | TATCCTTGATGAACA[A/C]AGATGCTAAAATCCT | 1130 |
rs758501976 | snp | G/T | 1.69645e-05 | 0.00291238 | intron-variant | LYST | GRCh38.p7 | 1:235801148 | CTAAACACTAAATAT[G/T]TCAAACTTCATTAAT | 1130 |
rs758502451 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769453 | AAAGCCCTTAGTGCC[A/T]CCGAAGCAAAGGCGC | 1130 |
rs758505971 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712562 | GTTTATTTATTGAAT[A/G]AATGAATAATGAAGA | 1130 |
rs758506488 | snp | C/T | 1.66846e-05 | 0.00288826 | intron-variant | LYST | GRCh38.p7 | 1:235781924 | CAATCATAGCTCACT[C/T]ACCGTTGAAGAGAAG | 1130 |
rs758522204 | snp | C/T | 1.64942e-05 | 0.00287173 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809115 | ATCTGGACACAAGTG[C/T]TGCTCAAGGAAGCCT | 1130 |
rs758523338 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235821832 | TCCCATTCTGCCCCA[A/C]CTCCCCTGCAGGCAA | 1130 |
rs758536565 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235750487 | GAATTTAAGACAGTA[A/G]GAGTGATTAAATTTC | 1130 |
rs758545714 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669297 | GCAGGAGAATAGGGT[C/G]TGGAGGCAGGGAACC | 1130 |
rs758549334 | snp | C/T | 1.65168e-05 | 0.00287369 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809679 | ACCTCCTGCAGTGTT[C/T]TCTTTTGTCTTGGTG | 1130 |
rs758551378 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830261 | GCTTGGTAAGTAATA[A/G]AAATCCTCGACCATG | 1130 |
rs758553111 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235681743 | ATCATCTCTTCACAC[C/T]GGGCCTTTCTTCCTT | 1130 |
rs758556793 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860557 | CATAGTTTTGCCTTT[C/T]CCAGAATGCCATACA | 1130 |
rs758558483 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235795079 | AGAAAGCTGCAACCT[A/G]GAATTCCTTTGAATT | 1130 |
rs758584910 | in-del | -/TTT | | | intron-variant | LYST | GRCh38.p7 | 1:235779307 | ATAATTTATGTTGAG[-/TTT]TGTAACTTATATGAC | 1130 |
rs758605873 | snp | C/T | 6.59055e-05 | 0.00574007 | synonymous-codon | LYST | GRCh38.p7 | 1:235693464 | TGACCACTGAATGTC[C/T]GTACTGTTCATGCTT | 1130 |
rs758609636 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883272 | CAGGTAGCTGCAACG[A/C]AACTGGTCTCTTCCA | 1130 |
rs758612138 | snp | A/C | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808756 | AAGCATCCCATTTCC[A/C]CAACAAATCTTCAGA | 1130 |
rs758613028 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737911 | TGCTGGAGCCGCTGC[C/T]GACGAGTCTGGATCT | 1130 |
rs758628091 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881069 | AAGTGACTTGCTGTA[C/T]GTGATATACAGGGCA | 1130 |
rs758654833 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235700374 | TACAAGGAACTGGTA[C/G]AAATTTACAAGAAAA | 1130 |
rs758658587 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235686885 | AGTGAATTATACTTC[A/T]TAAAGGCTTTCTTCC | 1130 |
rs758673996 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235704482 | ATCTCACTGTGGTTT[C/T]GATTTGCATTTTTCT | 1130 |
rs758677773 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235781758 | GAATCTTGGAAATAC[A/G]GTACTTATTAAACAC | 1130 |
rs758716853 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759117 | GAAAAGCTAGCCCAA[A/G]GCTTGCAATAGTGCT | 1130 |
rs758729250 | snp | A/T | 1.64784e-05 | 0.00287035 | intron-variant | LYST | GRCh38.p7 | 1:235755467 | TATAGTGGAGGGAAG[A/T]ACACACTTACTCTTC | 1130 |
rs758740364 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235830677 | AGGTAAGTAACAGCA[A/C]CTGGATGGAAAACAT | 1130 |
rs758743480 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235860099 | TAGTTTCTGGACTTT[A/G]CCTTCCTCTCCCCCC | 1130 |
rs758743616 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235795947 | TATATCCTTATATGA[A/G]AAAGAAATAACCAGA | 1130 |
rs758758700 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792025 | GATGAAACACCGTTG[C/T]TTAAATTTGGAGCGT | 1130 |
rs758792359 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771725 | ACATGGCAATAGTTA[A/G]TTGGCTGTTGGACAT | 1130 |
rs758794881 | snp | C/T | 1.65258e-05 | 0.00287448 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805755 | TACCTGATTAGGTAA[C/T]TCCAATTCCATCTTC | 1130 |
rs758803891 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873165 | ACTTTGGGGTATTGT[A/G]TTGAGTCCTGACATA | 1130 |
rs758826015 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235800488 | GGTATCTACTATATA[C/T]GTATATATGTATTTA | 1130 |
rs758829299 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831874 | TTATCCAACTTTAAT[A/G]TATTTCATTGAATCT | 1130 |
rs758835327 | snp | C/G | 1.6519e-05 | 0.00287388 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730857 | GTTACCTTATAGATT[C/G]ACTTGCAGCTTTGTC | 1130 |
rs758844269 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235818385 | CTCCAGGGCTCAGGC[A/C]CTAGTCCTCAGCAAT | 1130 |
rs758859512 | snp | A/G | 1.65482e-05 | 0.00287643 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759528 | GTGAAGAAGTAGGGA[A/G]TGCTGGTAGGCTTCT | 1130 |
rs758862332 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817439 | TTATGTTCACCACAG[C/G]ACTATTCACAATAAC | 1130 |
rs758866072 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235839339 | TCAGCTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 1130 |
rs758866117 | snp | C/G | 1.64914e-05 | 0.00287149 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810097 | CAGACAAGGCAGCTG[C/G]CTCACTTAAAATGTC | 1130 |
rs758873397 | snp | A/C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693186 | GCTGGGCGTGGTGGC[A/C/G]GGTGCCTGTAGTCCC | 1130 |
rs758885633 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235763015 | ATATGTGAATACTTA[A/C]TCTTCACAATTTTTT | 1130 |
rs758888571 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755550 | TCTTGAGTTCCTCGA[C/T]GAAGATACAACTGGT | 1130 |
rs758893362 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706000 | GTTTTGCCATGTTGG[C/T]CAGGCTGGTCTTGAA | 1130 |
rs758905040 | snp | C/T | 2.26868e-05 | 0.00336792 | intron-variant | LYST | GRCh38.p7 | 1:235693301 | GCTTGGGCGGCAGAG[C/T]GAGACTCCGTCTTAA | 1130 |
rs758953262 | snp | A/G | 1.93168e-05 | 0.00310773 | intron-variant | LYST | GRCh38.p7 | 1:235792133 | AGAATTTTCTAGAGA[A/G]AAAGAAAAACAAATG | 1130 |
rs758955552 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235803682 | AAAGAAGCTCAGAAT[A/G]CTTCATCATTGTAAC | 1130 |
rs758969824 | in-del | -/A | 1.96466e-05 | 0.00313415 | intron-variant | LYST | GRCh38.p7 | 1:235793471 | GTGAAAGAATTTATC[-/A]GTGAAAAATGTAAAA | 1130 |
rs759020968 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235782748 | GAAGTCTCCCATCTT[C/G]ACAAACAATTCCAAA | 1130 |
rs759027651 | in-del | -/TAGGTAGGTAT | 1.6473e-05 | 0.00286988 | frameshift-variant, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766224 | GCTATAATTTTCACA[-/TAGGTAGGTAT]AATGATCTACAAACC | 1130 |
rs759030993 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848832 | CTTAAATCAGGAAGA[A/G]TGAGATACCCTGAAC | 1130 |
rs759043746 | snp | C/G | 1.6501e-05 | 0.00287232 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770176 | TGCAAAACCTGACAA[C/G]TCAGTAGAAAGTGAT | 1130 |
rs759047844 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819233 | AAACACAATTCATCA[C/T]TGGGGAAGTTCTCTT | 1130 |
rs759051049 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806287 | TCAGGAGAAGGCAAG[A/G]CAAGGCTCTCGAGAG | 1130 |
rs759051535 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235880823 | TTGCTGCATTTTTTC[A/C]TTTAAAGAATTCCAT | 1130 |
rs759051619 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676983 | TGTTACCAAAGTATT[G/T]AGATCTGGCAGGGAC | 1130 |
rs759063948 | in-del | -/T | 3.35121e-05 | 0.00409328 | intron-variant | LYST | GRCh38.p7 | 1:235788886 | CAGTAAAATGGTTCG[-/T]TAACAACTGAGTAGA | 1130 |
rs759070281 | snp | A/G | 1.6557e-05 | 0.00287719 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801088 | TCTGTTTCAGACTTT[A/G]AGTCTACCCCTGAAA | 1130 |
rs759091400 | snp | A/G | 1.86545e-05 | 0.00305399 | intron-variant | LYST | GRCh38.p7 | 1:235813097 | TCCTTCATGTTCTAA[A/G]GCGATAAGACACATC | 1130 |
rs759108762 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235766026 | TGAATCAAGTGGGAA[G/T]AATAAAACAAAAGTG | 1130 |
rs759111310 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807029 | AGAAAAGATTGCCTG[C/T]CCCACATTAAATGAA | 1130 |
rs759114493 | snp | A/G | 3.30852e-05 | 0.00406712 | missense | LYST | GRCh38.p7 | 1:235693363 | ACCTGGTACTGTTGT[A/G]AACTTTGAATAAAGT | 1130 |
rs759124294 | in-del | -/GT | | | intron-variant | LYST | GRCh38.p7 | 1:235833164 | TGCTTTGTATATTAG[-/GT]GAAGTATTCACCTCT | 1130 |
rs759124516 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235725155 | TAAAGGGGAATAGGC[C/T]GGGTGCGGTGGCTCA | 1130 |
rs759132001 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235860363 | TCATTATCACCCAAA[A/G]TCCACAGTTTACATT | 1130 |
rs759134716 | in-del | -/GTATATAT | | | intron-variant | LYST | GRCh38.p7 | 1:235857717 | TATACACACACACAC[-/GTATATAT]ACACAAACATATGTA | 1130 |
rs759147683 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235666945 | ACTGCATGGCTTAAT[A/C]CTTCAAAATAAAAAA | 1130 |
rs759148295 | snp | G/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802922 | CCATCATCCTGGGTT[G/T]CGCCATCTTCAGGAT | 1130 |
rs759155601 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235747574 | TCATATCCTGTATAT[A/G]TTCAAGAGTTTTACT | 1130 |
rs759156433 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698502 | TAGGGTCAGGCATTT[C/T]GAAAACAAGCTTCTA | 1130 |
rs759166650 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734253 | AAAATCTTTCCTTCA[C/T]TGAAGGCTACTGATA | 1130 |
rs759166964 | snp | A/G | 3.30366e-05 | 0.00406413 | intron-variant | LYST | GRCh38.p7 | 1:235733734 | TTAAGCATACATGGA[A/G]CGTATTTATCAGAAC | 1130 |
rs759168232 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702856 | AGCTTGGCTCCAGGT[C/G]TGCTCACATGGGCCA | 1130 |
rs759176121 | snp | A/G | 1.66955e-05 | 0.0028892 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752077 | CAATAACCCTAAAAT[A/G]TTGTGAGCCTGAGGA | 1130 |
rs759179444 | snp | A/G | 1.94695e-05 | 0.00311999 | intron-variant | LYST | GRCh38.p7 | 1:235812951 | TAACACAAGTGATAT[A/G]ATAAAGGGAAAAAGC | 1130 |
rs759207082 | snp | G/T | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724029 | AAGGGTGAATTTACC[G/T]TGGTGTTATCAAATG | 1130 |
rs759221539 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235709589 | GAAAAGGAGAAAACC[A/T]TTGCCTACTAATTCC | 1130 |
rs759246340 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235685533 | AACAAGAGTTCAAAA[C/G]GGAATAAGCTTGGAA | 1130 |
rs759253594 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235749126 | TCTATGTCCCTTTAG[G/T]ATCATGGACAAATGG | 1130 |
rs759276899 | snp | C/T | 8.27767e-05 | 0.00643284 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788801 | CTTCTTCTATGAGTC[C/T]TTCACCAGGATTTAT | 1130 |
rs759292386 | snp | A/G | 6.6422e-05 | 0.00576252 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808857 | CATAAGTTTCCCTGC[A/G]GTGTCTCTTCTAATT | 1130 |
rs759296565 | snp | A/G | 5.32354e-05 | 0.00515896 | intron-variant | LYST | GRCh38.p7 | 1:235712214 | TATAAAAAAATACAA[A/G]TAATACGATTAAGAC | 1130 |
rs759301908 | snp | A/G | 3.5202e-05 | 0.00419521 | intron-variant | LYST | GRCh38.p7 | 1:235830461 | AAAAAAAGATTAGGA[A/G]AACAAATACAAATTT | 1130 |
rs759318058 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235742324 | GCTGGGTGTGGTGGT[-/G]GGTGCCTGTAATCCC | 1130 |
rs759336491 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | LYST | GRCh38.p7 | 1:235755443 | GAAAAAAGACAAAAG[A/G]TTCCCAATTATAGTG | 1130 |
rs759346488 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859373 | CAAACCTTCCCAATG[A/G]TCACATCTACTTCCT | 1130 |
rs759349999 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792584 | CCTCCCAAAGTGCTG[G/T]GATTACAGGCGTGAG | 1130 |
rs759350175 | snp | C/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791964 | AACTCGTGCTCTTCT[C/G]AATAAACCCATGGCC | 1130 |
rs759371628 | snp | A/C | 3.55581e-05 | 0.00421637 | intron-variant | LYST | GRCh38.p7 | 1:235766321 | ATTTAAAGAATTGTC[A/C]ACTTAACTAAGATTT | 1130 |
rs759394187 | snp | A/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755513 | TCGACCAAAGAACAT[A/T]TCGATGAAGCATTCT | 1130 |
rs759409037 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672978 | AAACTCCCAGTTCAC[C/T]GACACCAACCCGGAG | 1130 |
rs759416818 | in-del | -/GT | | | intron-variant | LYST | GRCh38.p7 | 1:235857717 | TATACACACACACAC[-/GT]ATATATACACAAACA | 1130 |
rs759419129 | snp | C/G | 3.29457e-05 | 0.00405854 | missense | LYST | GRCh38.p7 | 1:235687019 | GTAAACAGCTGGCAA[C/G]TGTCAGGCACCCAAG | 1130 |
rs759423696 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235882843 | ATTGAGTGAGTCCTT[-/A]ATAACTACGCCATGA | 1130 |
rs759431787 | snp | A/T | 3.33133e-05 | 0.00408112 | intron-variant | LYST | GRCh38.p7 | 1:235804708 | TATTAATAACCATTT[A/T]AAAAAACTAAATGAT | 1130 |
rs759434385 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828715 | AAAGAAGACAAAGCA[C/T]TGAATTTTTTTATTG | 1130 |
rs759443312 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235719499 | ATCATCAATGGATGA[A/G]ACCATTAGGTACAAA | 1130 |
rs759454701 | in-del | -/TCAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235872294 | GAGTGACATTCTGTC[-/TCAAAA]AAAAAAAAAAAAAAA | 1130 |
rs759457595 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235760423 | CTTGCTGTTATTAGT[A/G]AGAATAGTTTCTTTT | 1130 |
rs759458758 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838724 | AATCTGACCGTGAGA[C/T]GTGAATTCATTTTAG | 1130 |
rs759481531 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718676 | TTCTTTAAACTAAAC[A/C]TCAGAATATTTTTTC | 1130 |
rs759510542 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235852446 | AAGCCAGTTAGACAT[A/G]TTGAGGTAATCTCAG | 1130 |
rs759526929 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806618 | CAATGTCTATCCCAT[C/T]AATATCTGGAACTGA | 1130 |
rs759547330 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809283 | GAGAGATCTCGGTGA[C/T]GATGCATAAAATGAG | 1130 |
rs759553487 | snp | C/T | 3.03375e-05 | 0.00389459 | intron-variant | LYST | GRCh38.p7 | 1:235800849 | TAAATATTGATCACA[C/T]TTAACTAAATGAATT | 1130 |
rs759557692 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235862618 | CTGGGCAACACGGTG[A/C]AACCCCATGTCTACT | 1130 |
rs759560536 | snp | C/T | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746337 | TCCTATAGTCTTACC[C/T]TGATAAATAATCCTG | 1130 |
rs759564190 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235816725 | ACAGACACAGAGACC[A/G]ATGGAACAGAATAAA | 1130 |
rs759592266 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720702 | AAGTGTCTCACTAAC[A/G]TAGTCAGCAAGTATA | 1130 |
rs759592931 | snp | A/C | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661512 | CCTAGGTATCACTAC[A/C]TGTGTATGCAGTTTA | 1130 |
rs759610707 | snp | A/G | 1.65198e-05 | 0.00287395 | intron-variant | LYST | GRCh38.p7 | 1:235728173 | TTTTAAAATGTATGT[A/G]CACACTACCATTCAT | 1130 |
rs759611338 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235690084 | ATTTGATTGAAAGCT[-/TA]TGTTATATCTTTAAC | 1130 |
rs759632151 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235760252 | GGGTTCAGAATATCT[A/G]CTTTGCAGGGTGGCT | 1130 |
rs759646432 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813964 | GTGTTAGAGGCAGGG[-/T]AACAATAATCCAGAT | 1130 |
rs759658857 | snp | A/G | 6.59207e-05 | 0.00574073 | intron-variant | LYST | GRCh38.p7 | 1:235663936 | CTCTCTACGAAAAAT[A/G]CAATCACAAATTGTA | 1130 |
rs759664464 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235688221 | ACCTAAGTTACATTA[C/T]AAGATCTTAATAACT | 1130 |
rs759672980 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693051 | CCAGGTGTGGTGGCT[C/G]ACACCTGTAATCCCA | 1130 |
rs759720507 | snp | C/T | 4.94833e-05 | 0.00497385 | missense | LYST | GRCh38.p7 | 1:235697203 | GGCTGAAGCAGACCA[C/T]AGGTACTGGAGCACT | 1130 |
rs759733310 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751300 | CAGAGTCATGATTTG[C/T]GGTGGTCCTTATAAA | 1130 |
rs759740477 | snp | C/T | 1.65529e-05 | 0.00287683 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235738600 | TCTAGTGTGCCTGTA[C/T]GGAGTAAAGCAAATG | 1130 |
rs759744034 | in-del | -/AAA | | | intron-variant | LYST | GRCh38.p7 | 1:235744893 | GTGAGAACCCATCTC[-/AAA]AAAAAAAAGAAAAAA | 1130 |
rs759755122 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701606 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 1130 |
rs759755782 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235836586 | TGAGTGCAAGAGGAC[A/G]AGAGGTAAAAAATAA | 1130 |
rs759773181 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759426 | TTTGTTTCTTTGATT[G/T]GGTGGCAACATAAGT | 1130 |
rs759784697 | snp | C/T | 1.6498e-05 | 0.00287206 | synonymous-codon | LYST | GRCh38.p7 | 1:235664055 | CCATGTGCTCCATAA[C/T]CTAGAGGGGAAAAAA | 1130 |
rs759793787 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785692 | TAGTCTCACCATGTC[C/T]ATTCATTTTTATTTC | 1130 |
rs759850572 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235876665 | CCTATGATGTGACAT[C/T]CTGTTTGTTAGTAAA | 1130 |
rs759859570 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235681109 | AACTCCGGGGACCCA[C/T]AGATAAGTCGCTTCC | 1130 |
rs759864415 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809979 | ACACTGGCTGCTAAA[A/G]GAGAATTATGATTCA | 1130 |
rs759868763 | snp | C/T | 4.94645e-05 | 0.00497291 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810378 | CGATGGGTAATTTTA[C/T]GCTGTCGTCTGCTTT | 1130 |
rs759876510 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731166 | TAGTAGATGGGGTCA[C/T]ACCATACTGCTCTGC | 1130 |
rs759885118 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235713574 | GGGTTATTTGGCAAT[A/G]TCTAGCAACATTTTT | 1130 |
rs759886632 | snp | C/T | 1.65121e-05 | 0.00287329 | missense | LYST | GRCh38.p7 | 1:235677174 | TGTCCCGCCAGACTT[C/T]GTACATAGCATAACC | 1130 |
rs759896864 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235700289 | TACCATCAGAGTGAA[C/T]AAGCAACCTATAGAA | 1130 |
rs759939100 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823009 | CCAAAGTGGCTATTC[C/T]AGCTGAGCCATGCCA | 1130 |
rs759944436 | snp | A/C/T | 4.94387e-05 | 0.00497165 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731146 | CCAACTGCCATGAGG[A/C/T]TGGATAGTAGATGGG | 1130 |
rs759945342 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235682108 | TGAGCCCAGGAGCTC[A/G]AGAATAGCCTGAGCA | 1130 |
rs759946307 | snp | A/G | 1.65397e-05 | 0.00287569 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744082 | TCCTCAGAAATTTCG[A/G]TCTGGAAAACTGAGG | 1130 |
rs759980441 | snp | C/T | 8.30075e-05 | 0.00644181 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808648 | TCCACTGAACAACTA[C/T]ATTGCCTTTCTGGAT | 1130 |
rs759993717 | snp | A/G | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810453 | CTTCCTTCTAAATGT[A/G]ATTTTTCCTGAGTGG | 1130 |
rs759993786 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235700043 | TAGCCATATGCAGAA[A/C]ACTGAAACTGGACCC | 1130 |
rs759996719 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235752516 | GTTTCTAGTCCACAC[G/T]AAGGATGAAGATTGT | 1130 |
rs760009092 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687872 | ATCCTCAGGCTTCCT[C/T]AGAAACCTTGTTTTC | 1130 |
rs760029238 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235824590 | TATGGTAGAAATATT[C/T]AACTTTGTCATCTTT | 1130 |
rs760030965 | snp | A/T | 1.75674e-05 | 0.00296368 | intron-variant | LYST | GRCh38.p7 | 1:235716800 | GAAAAGGACAATTTT[A/T]AAAATTAAATATTTT | 1130 |
rs760051696 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235842572 | AGAACACAGCTAACA[A/G]CAGGCATTCGATTCT | 1130 |
rs760069169 | snp | G/T | 1.65015e-05 | 0.00287237 | intron-variant | LYST | GRCh38.p7 | 1:235731194 | TGCAAGTAAAAAGAT[G/T]AAAGGGTGTTTTAAG | 1130 |
rs760102615 | in-del | -/GCTC | | | intron-variant | LYST | GRCh38.p7 | 1:235728825 | CCCAGCAGGCTTGAA[-/GCTC]CATATCTTGGACCTT | 1130 |
rs760108842 | snp | A/G | 4.94792e-05 | 0.00497365 | splice-donor-variant, downstream-variant-500B, intron-variant | LYST | GRCh38.p7 | 1:235751208 | ATGATTTCAATACTC[A/G]CCAGCAATGCTTTTC | 1130 |
rs760115299 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235720173 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 1130 |
rs760116262 | snp | C/T | 1.67365e-05 | 0.00289275 | intron-variant | LYST | GRCh38.p7 | 1:235788885 | ATCAGTAAAATGGTT[C/T]GTAACAACTGAGTAG | 1130 |
rs760118012 | snp | A/G | | | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775030 | GTATTTAATTAATGA[A/G]AGTATAACTCGCAGT | 1130 |
rs760122503 | snp | C/G | 1.67072e-05 | 0.00289021 | intron-variant | LYST | GRCh38.p7 | 1:235803087 | TCAGTGTAATTCAAA[C/G]GTTGTAACATTTGCT | 1130 |
rs760130977 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865447 | GAAGGAGCAGATATT[-/TA]TGTTTTCTTAGAAAA | 1130 |
rs760158341 | snp | A/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868669 | AATGCCATTTGTGAC[A/T]ATTATTTTTTTCGGT | 1130 |
rs760160524 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235833248 | AACTGAAGAGATGAT[C/T]GCACGGTATTTTCTT | 1130 |
rs760174550 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738549 | GGAGTTCACACATTA[A/G]GCTGTCATGGGTGAG | 1130 |
rs760187462 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon | LYST | GRCh38.p7 | 1:235662943 | GTTCATTCGCATTCA[C/T]CCGGCTGCATAGCTG | 1130 |
rs760193138 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235723788 | TTGTCAAAGATGGAC[C/G]CTGCTACAGCACTGA | 1130 |
rs760214066 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802925 | TCATCCTGGGTTTCG[C/T]CATCTTCAGGATTGC | 1130 |
rs760231608 | snp | A/C | 1.65586e-05 | 0.00287733 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809721 | GGCTGCTTTTCTAGG[A/C]ATATTCTAATTTTTA | 1130 |
rs760234470 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235881891 | GAGTTAGTGTTCAAT[A/G]GGTACAAAATTTCAG | 1130 |
rs760244391 | snp | A/G | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753113 | CCATTATCCAGCAAC[A/G]TATCTGCTACCTTAG | 1130 |
rs760254735 | in-del | -/A | 1.64814e-05 | 0.00287061 | intron-variant | LYST | GRCh38.p7 | 1:235693506 | AGGAGAAGGAGAAAG[-/A]AAAGTATCAGATTGT | 1130 |
rs760263846 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235839300 | CTCGCTCTGTCGCCC[A/C]GGATGGAGTGCAGTG | 1130 |
rs760264229 | snp | A/C | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739655 | GTCAAATAGTTGACA[A/C]GGGAAAGTTCTTCCC | 1130 |
rs760273253 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848920 | ACCAGACAGATTCAC[A/G]GCAGAATTCTACCAG | 1130 |
rs760274731 | in-del | -/ATTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235832651 | TATTACATATATAGC[-/ATTAT]ATTATAGTTTACTAT | 1130 |
rs760288574 | snp | A/C | 1.69241e-05 | 0.00290891 | intron-variant | LYST | GRCh38.p7 | 1:235830218 | AGTATTTGATATAAA[A/C]ATGTTACCTGATCAA | 1130 |
rs760296070 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763964 | TCCAGTGGCTTTCTA[C/T]GCCTCCTTACCACCT | 1130 |
rs760297715 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235708400 | GTTAACATAGCAAGA[C/T]TGACTGCTATCTCTG | 1130 |
rs760301959 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235782322 | TACAGGTGCCCGCCA[C/T]CAGGCCTGGTTAATT | 1130 |
rs760309200 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724044 | TTGGTGTTATCAAAT[A/G]CCAACAGGAGTGTTC | 1130 |
rs760309897 | in-del | -/AAAGA | | | intron-variant | LYST | GRCh38.p7 | 1:235858972 | TCATCATGATTCAGC[-/AAAGA]AGTCACATGCCCCTA | 1130 |
rs760310039 | snp | A/C | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746462 | TCACATGAAGCTCAT[A/C]ATTTGCCACTGAACG | 1130 |
rs760310306 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761562 | AATTACAGGGCAGCC[-/T]TTTAAAGCTCTGCTA | 1130 |
rs760317441 | in-del | -/G | 1.65272e-05 | 0.0028746 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804626 | TTGACTGGGAAAGAT[-/G]GTCCCTCATTTCAAA | 1130 |
rs760333915 | in-del | -/G | 1.64838e-05 | 0.00287083 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791773 | TTTCCTTTTTCTGTA[-/G]TACTCTCAGCTTCAT | 1130 |
rs760344189 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon | LYST | GRCh38.p7 | 1:235709133 | AACAGAAGCCTTCCC[C/T]TTTTGCTTATACCCA | 1130 |
rs760345150 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235818637 | TGTACATGGTCTTTT[-/A]AAAAAAAAAAAAGAT | 1130 |
rs760346093 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235675744 | GTGTTTTACTGAGTT[A/C]TGTGAGTCATTCTAG | 1130 |
rs760355383 | in-del | -/CA | | | intron-variant | LYST | GRCh38.p7 | 1:235724975 | TGTATGCACATACCC[-/CA]GTTTCAGAAACAAAT | 1130 |
rs760363185 | in-del | -/T | 1.65015e-05 | 0.00287237 | intron-variant | LYST | GRCh38.p7 | 1:235730994 | ATGACCATAGTTCTC[-/T]GCTATATTTATATGT | 1130 |
rs760365263 | in-del | -/CTTA | | | intron-variant | LYST | GRCh38.p7 | 1:235757481 | AGAGACCAAAAAAGT[-/CTTA]CTAACATGACAAGAA | 1130 |
rs760383965 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765901 | CCACTTGGCATTTAG[A/T]CTCCTTGAGGACAGA | 1130 |
rs760385237 | snp | A/C | 1.64944e-05 | 0.00287175 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809092 | CAATGTTATGAACAC[A/C]CGATAGGATCTGGAC | 1130 |
rs760385685 | snp | A/T | 3.32618e-05 | 0.00407797 | intron-variant | LYST | GRCh38.p7 | 1:235791685 | GTACAAATCAGATAA[A/T]CCTGTCATCATACCT | 1130 |
rs760393508 | snp | C/T | 3.29707e-05 | 0.00406008 | intron-variant | LYST | GRCh38.p7 | 1:235804456 | ATCCCACACTTCCGC[C/T]TCTGCTGGTCATACC | 1130 |
rs760413017 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235862217 | ACCCTAATAAGAAAA[C/G]TAACTTTAAATGACC | 1130 |
rs760418480 | snp | A/G | 1.67211e-05 | 0.00289142 | intron-variant | LYST | GRCh38.p7 | 1:235755658 | AATAGCTAAACAAAA[A/G]ATTTAAGTCAATTTA | 1130 |
rs760432992 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | LYST | GRCh38.p7 | 1:235693399 | GGAGGCTCACTTTGT[C/T]TACTCTTCAACCTTA | 1130 |
rs760434110 | snp | A/T | 1.68329e-05 | 0.00290106 | intron-variant | LYST | GRCh38.p7 | 1:235703021 | ACATATGTAGTAAAA[A/T]GAAAGACTTGACAAT | 1130 |
rs760436039 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665269 | AAATACTTGGAAAGC[C/T]AAACAGTCTCCAAAA | 1130 |
rs760439692 | snp | C/T | 1.83293e-05 | 0.00302726 | intron-variant | LYST | GRCh38.p7 | 1:235777024 | CAATAATAAGTAAGT[C/T]ATTTCTCTTTAGACA | 1130 |
rs760492925 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235847931 | TGAGACAGCAACACA[A/G]TAATAGTGGGGGACT | 1130 |
rs760516059 | in-del | -/TGCCCAGGCTGGGGTGCGG | | | intron-variant | LYST | GRCh38.p7 | 1:235690954 | AGAGTCTCGTTCTGT[-/TGCCCAGGCTGGGGTGCGG]TGCCCAGGCTGGAGT | 1130 |
rs760520021 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861400 | GACCTCTCTCATTAC[C/T]GTAAACAAAGTTGGG | 1130 |
rs760522481 | snp | C/T | 2.90263e-05 | 0.0038095 | intron-variant | LYST | GRCh38.p7 | 1:235733934 | GATAATAATATACTA[C/T]ATAAAATTTATTATT | 1130 |
rs760538931 | snp | A/C/G | 4.05476e-05 | 0.0045025 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746524 | AGGGGAAATTTTCGA[A/C/G]GACCTTTAAAAGTAT | 1130 |
rs760539546 | snp | C/T | 1.66701e-05 | 0.002887 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792077 | ACTGTGAAGGGCTCA[C/T]AGTAGTATCACTTTC | 1130 |
rs760540960 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674631 | ACTAGGGATGCCATT[A/T]AAGGAATAGCTGAAC | 1130 |
rs760559863 | snp | A/T | 1.64912e-05 | 0.00287147 | intron-variant | LYST | GRCh38.p7 | 1:235693533 | TTGTCACTGCTCGAC[A/T]GTTACATGACAGCCC | 1130 |
rs760562286 | snp | C/T | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746447 | TTCTCCGTTGCATCA[C/T]CACATGAAGCTCATC | 1130 |
rs760574626 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715295 | GGAGCCATAGTGATA[A/G]GGCTGCACGGGAGGC | 1130 |
rs760580414 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235745365 | GCAAATTAAAACCAC[A/C]ATGAGATATCACTAC | 1130 |
rs760581656 | snp | A/G | 3.30049e-05 | 0.00406219 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806369 | CAGAAGTATCTTCTG[A/G]GTCATTGGCCGACTC | 1130 |
rs760583220 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235791065 | GAGGTGGGCAGATCA[C/G]CTGAGGTCAGGAGTT | 1130 |
rs760609781 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235860472 | CAGAATAGTTTCACC[A/G]CCCTAAAAATCTTCT | 1130 |
rs760611931 | in-del | -/TTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235778370 | GATTATTCTTATTAT[-/TTAT]TTATTTATTTATTTA | 1130 |
rs760613723 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875465 | AACTATAATAACACA[A/G]TATTCTGACTCTCCA | 1130 |
rs760632806 | in-del | -/A | 0.00117705 | 0.0242309 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808444 | CGCCGCCACCCACAC[-/A]ACATACAAACCTGGA | 1130 |
rs760641389 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840453 | TGAAAGGCTTTTGTA[C/T]ACTATGCTAAGAACC | 1130 |
rs760649559 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848743 | ATTCAAGGCTACTAC[A/G]AATACATTTACAGAC | 1130 |
rs760651217 | snp | C/T | 3.31554e-05 | 0.00407144 | missense | LYST | GRCh38.p7 | 1:235664543 | GAGAAAGCCACGGAA[C/T]AGATGATCTCCCTGC | 1130 |
rs760652216 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771840 | TCTATAGGAAGAATA[C/G]AAAATTCTCTTTCCT | 1130 |
rs760654779 | snp | A/G | 3.48949e-05 | 0.00417687 | intron-variant | LYST | GRCh38.p7 | 1:235773820 | CACAATAAAAAATGG[A/G]AAAAAAGTACATATT | 1130 |
rs760661502 | snp | C/T | 1.8739e-05 | 0.00306091 | intron-variant | LYST | GRCh38.p7 | 1:235805695 | ATGTGTGTGTGTATA[C/T]ATATGTATATATATT | 1130 |
rs760685971 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235838332 | TACTATAATCCAACT[C/G]TCCTTCATGTTCCCA | 1130 |
rs760686962 | snp | A/T | 1.65179e-05 | 0.00287379 | intron-variant | LYST | GRCh38.p7 | 1:235733743 | CATGGAACGTATTTA[A/T]CAGAACATGATACTT | 1130 |
rs760697809 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672246 | GTATAATTTGGAACT[G/T]GAAAAATAAATTTAG | 1130 |
rs760701987 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235873921 | CTGAGCAGATTAAAA[A/C]TTACAAGGACTCGCT | 1130 |
rs760704647 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828427 | GAATTTTAAGATATG[C/T]GAATTATATCTCAAT | 1130 |
rs760705038 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813614 | ACCCTTTCTGGAGGA[A/T]ATGGTCCAAGCCCTG | 1130 |
rs760722418 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235736819 | GTGTAAATACATGTA[-/T]TACATAGATTTGCTT | 1130 |
rs760724646 | in-del | -/AGG | | | intron-variant | LYST | GRCh38.p7 | 1:235846551 | CCTGACAAAGAATTC[-/AGG]AGGTTAGATATTAAG | 1130 |
rs760725116 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854342 | AGGGCCAGGATTCAG[A/G]CTCATGCAATCCCTT | 1130 |
rs760727044 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235839044 | TGTCCAGGCTGGTCT[A/C]GAACTTCTGGGCTCA | 1130 |
rs760735266 | snp | C/T | 2.97305e-05 | 0.00385543 | intron-variant | LYST | GRCh38.p7 | 1:235806816 | GTTTAAATAAAGAAA[C/T]ATCATTTATAAATAG | 1130 |
rs760736599 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717218 | AACAGAGGAAGATGC[C/T]GTGTTATTAGCCTAG | 1130 |
rs760751774 | snp | A/C | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806704 | GAATGACTTCGAATA[A/C]CATTTAAGCAATTTA | 1130 |
rs760752760 | snp | A/G | 4.94931e-05 | 0.00497434 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770241 | AAACATCTGCTGGTG[A/G]TGATCTGCTCTGATG | 1130 |
rs760771720 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235840166 | CTCTGCCCTCAAGAA[A/G]ATTACATTACGGTGG | 1130 |
rs760786459 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235692314 | CTCCAGCCTGGGCGA[C/T]GGAGCGAGACTTCAT | 1130 |
rs760815034 | snp | A/C | 0.000164718 | 0.00907368 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702835 | GGAAGCTCTCCTTCA[A/C]TATTGAGCTTGGCTC | 1130 |
rs760817250 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853265 | AAGTAACACCTTCAG[C/T]TCTAAAGAGCATCAG | 1130 |
rs760827955 | snp | A/G | 8.28123e-05 | 0.00643423 | intron-variant | LYST | GRCh38.p7 | 1:235730805 | CTACAATAAGCTGTT[A/G]TATATTCATGAAAGA | 1130 |
rs760854107 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235742063 | ATCTAGAACAGTCAA[A/T]CTCACAGAGACAGAA | 1130 |
rs760875267 | snp | A/T | 1.65433e-05 | 0.002876 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738618 | AGTAAAGCAAATGTT[A/T]CTGGTGTCTCCCTCA | 1130 |
rs760878646 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755523 | AACATTTCGATGAAG[C/T]ATTCTAACAATTCTT | 1130 |
rs760879892 | snp | A/G | 1.65592e-05 | 0.00287738 | intron-variant | LYST | GRCh38.p7 | 1:235664094 | ATTATGCAAACTAAA[A/G]TTACTCTCCCTAAAA | 1130 |
rs760884217 | snp | A/G | 4.95135e-05 | 0.00497537 | intron-variant | LYST | GRCh38.p7 | 1:235730949 | TTGACAACATCTGTT[A/G]AGGAGAAAAGTAAAT | 1130 |
rs760887236 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235802080 | GCTCCTGAAATCCTA[A/G]CTACTTGGGAGGCAG | 1130 |
rs760891661 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868304 | TATCACTCATTTAAG[C/T]AGTATATAATGAGCA | 1130 |
rs760895365 | snp | A/T | 3.32033e-05 | 0.00407438 | intron-variant | LYST | GRCh38.p7 | 1:235757490 | AAAAGTCTTACTAAC[A/T]TGACAAGAAAAGTAC | 1130 |
rs760898723 | snp | C/T | 3.50201e-05 | 0.00418436 | intron-variant | LYST | GRCh38.p7 | 1:235759610 | CTCTCCTGGTAAGAG[C/T]AGATACAAAAATACT | 1130 |
rs760907074 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235852470 | ATCTCAGCACTTTGC[C/T]GGACCTTTTTCCCGG | 1130 |
rs760913625 | snp | A/C | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865299 | AAATTGCAAACCTCT[A/C]CCGGTTCCCTGCCCT | 1130 |
rs760913817 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235836453 | ATGGACAAGGAAGGT[C/T]TGAAGCAGTAATATT | 1130 |
rs760919824 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693342 | ATAAAATAAAATAAA[C/G]TGTTTACCTGGTACT | 1130 |
rs760927327 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235761140 | AAACTAATAAAAACA[A/T]AGCCTTAAAATATTA | 1130 |
rs760957735 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661311 | TTAAAAAAAGATGAG[C/T]AGCAACCCTATTCTA | 1130 |
rs760970189 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835337 | TAGCTGCTCTGACTA[C/T]TACCACCCTCCAGCT | 1130 |
rs760977323 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865999 | GTCGCTGGGTGTGTA[C/T]GGTCTGCCGAGCGGA | 1130 |
rs760983163 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693008 | CCTGGGCAACAGAGC[A/G]ACACTCTAAAATTAA | 1130 |
rs760985186 | in-del | -/TT | | | intron-variant | LYST | GRCh38.p7 | 1:235749320 | ACAACTTAGAAACAA[-/TT]TTAGAAAGCAACAAC | 1130 |
rs760992008 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882387 | CTCCTGTGTGCCATG[C/T]GGAAGCTTTGGACTT | 1130 |
rs760998361 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235821674 | AAATATTTTAGACTT[A/G]GTGAGTCATATATGG | 1130 |
rs761007324 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235881658 | CATACACGTACATAC[-/AT]ATATATATATGCAAT | 1130 |
rs761024661 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845448 | AGGAATTCTCTAGCC[C/T]AACTTTCTAACAATT | 1130 |
rs761049147 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235711010 | CCTGAAGGCAACAGC[A/T]TGAGACACCCTGAGC | 1130 |
rs761060524 | in-del | -/ATC | | | intron-variant | LYST | GRCh38.p7 | 1:235774264 | TTTTAAATTGAATTA[-/ATC]TGCTATTAGGCTTTA | 1130 |
rs761062972 | snp | C/T | 1.67435e-05 | 0.00289335 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766260 | GGGCATGGGTGTGAG[C/T]TGCCCCTCTTTGTAT | 1130 |
rs761069195 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878917 | GATTTAGGGGTGCAA[A/G]TGCAATTGTATTACA | 1130 |
rs761071378 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235678813 | TCCATTATGTTACTA[C/T]AGCCATAAACAACAT | 1130 |
rs761072673 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733554 | TGTCTGCTGGCACTC[A/C]AATCTACTTTATACA | 1130 |
rs761086974 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669009 | TCCTGAACACAAGAA[C/T]AGATGAATGTTTTGT | 1130 |
rs761110668 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859070 | TGTTCTTCCTTCTCA[A/G]TCTCAGCAGATAATC | 1130 |
rs761123844 | snp | A/C | 1.65026e-05 | 0.00287246 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809407 | CACTATTTATTAGGG[A/C]TTTCAAATGCTCTGA | 1130 |
rs761149802 | snp | A/C | 1.66391e-05 | 0.00288431 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800361 | AAAATACTCAAGAAC[A/C]CTCCTAAAAGATTTT | 1130 |
rs761153892 | snp | A/C | 3.303e-05 | 0.00406373 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806178 | ATGGCATACTCGGAA[A/C]CCACCAAGCCTATAA | 1130 |
rs761154790 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235677376 | ATGTGTTTCATGGTT[A/C]AAATGATTATAACGT | 1130 |
rs761178375 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235678390 | AAATTGGTGATGTTA[-/C]CAACGGTAATGGGCC | 1130 |
rs761189650 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702749 | CCAAATGACATACCG[A/G]ATAGGTGATTTCTTT | 1130 |
rs761199215 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720708 | CTCACTAACGTAGTC[A/G]GCAAGTATAAATGGG | 1130 |
rs761244658 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791866 | TTTTGCCCCAGCAAC[A/G]GCAGGTGGACTGGGG | 1130 |
rs761246087 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon, missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751361 | TAGTGCAACAGCCAT[A/G]TCTAAAAACAGAAGA | 1130 |
rs761246263 | snp | C/T | 0.000115377 | 0.00759443 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777178 | GGTTCTAATAAGATG[C/T]TCTGAACTTCTTTTG | 1130 |
rs761248841 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822799 | ATCAACATGTTGTTA[C/T]GTGACTTCTTGCAGC | 1130 |
rs761261371 | snp | A/G/T | 8.28266e-05 | 0.00643485 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235758998 | TGCAGTTCGGTTGTA[A/G/T]TTTGGCTCATAACCA | 1130 |
rs761280851 | snp | A/G | 9.8881e-05 | 0.0070307 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751302 | GAGTCATGATTTGCG[A/G]TGGTCCTTATAAATT | 1130 |
rs761284269 | snp | A/G | 3.29755e-05 | 0.00406038 | synonymous-codon | LYST | GRCh38.p7 | 1:235709169 | CAAGTCAATCCACTG[A/G]CAGATGTTCTGCGAC | 1130 |
rs761295933 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713419 | AACAAGAGTAGCACA[C/T]TGGGTAGGTTCTGTT | 1130 |
rs761299001 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235735223 | CAGAAAAACTGAACT[A/G]GAAGGGAAAGCTTCC | 1130 |
rs761310425 | snp | A/C | 6.59707e-05 | 0.00574291 | intron-variant | LYST | GRCh38.p7 | 1:235787386 | ACACTACAGAAAAAG[A/C]GAAAAGGCATAGGCT | 1130 |
rs761311238 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235786333 | TCAGAGAAATGCAAA[-/T]CAAAACCACAATGAG | 1130 |
rs761331058 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738332 | CTTAATTTGGTCCAG[C/T]GTAATGTGAACATCT | 1130 |
rs761332513 | snp | C/T | 4.975e-05 | 0.00498724 | intron-variant | LYST | GRCh38.p7 | 1:235791696 | ATAATCCTGTCATCA[C/T]ACCTGTACCATCAAA | 1130 |
rs761334667 | snp | A/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809729 | TTCTAGGCATATTCT[A/G]ATTTTTAAAGCTGCT | 1130 |
rs761343127 | snp | A/G | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753128 | ATATCTGCTACCTTA[A/G]AACAAGAATTTAAAA | 1130 |
rs761345760 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773922 | TAGCATTAGAGTCTA[C/T]ATCCAACTTAAACTC | 1130 |
rs761351181 | snp | A/G | 1.71616e-05 | 0.00292925 | missense | LYST | GRCh38.p7 | 1:235709276 | TGACGTGATTAACCC[A/G]TTCACCATTCTGACG | 1130 |
rs761352612 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674834 | AGCAAATAAATTAGC[C/T]GAAAAGTCATAGAAA | 1130 |
rs761366133 | snp | A/G | 1.78806e-05 | 0.00298998 | intron-variant | LYST | GRCh38.p7 | 1:235744193 | TACAAAATTAGTCAT[A/G]TCACTGCTATCTTGC | 1130 |
rs761398316 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235737505 | ATCATCTCCTTAAAA[A/G]GATATAAGGTCTTCT | 1130 |
rs761401307 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235744905 | CTCAAAAAAAAAAAG[-/AA]AAAAAAAAAGAGAGA | 1130 |
rs761405024 | in-del | -/TGTGTA | | | intron-variant | LYST | GRCh38.p7 | 1:235730610 | GTGTGTGTGTGTGTG[-/TGTGTA]TATGTAAACTAACAA | 1130 |
rs761410237 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804530 | TAGCATCATTATGTT[C/G]AAAATCTGCTGAATA | 1130 |
rs761421047 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235722271 | GGACTTTGCCTTTAA[C/G]TGAATGTGACATGAA | 1130 |
rs761441298 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728125 | ACAAAATACATTCCA[C/T]ATTTACCTGCAGAAA | 1130 |
rs761450259 | snp | A/G | 1.65195e-05 | 0.00287393 | intron-variant | LYST | GRCh38.p7 | 1:235731209 | TAAAGGGTGTTTTAA[A/G]TGACCATCCAGGACT | 1130 |
rs761452050 | snp | A/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762289 | TGAAAGCATTCTTGA[A/T]GATGATAAAGTCCAA | 1130 |
rs761461799 | in-del | -/CACATA | | | intron-variant | LYST | GRCh38.p7 | 1:235857782 | ACACACACACACACA[-/CACATA]TATATATAAAATTTC | 1130 |
rs761466745 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235869747 | TGCATTGGCTCTCCG[C/T]TTCTCTCAGATAAAA | 1130 |
rs761485607 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235767189 | GTGGGTAGCAGCTGG[-/C]CTCCAGATTAAGGGT | 1130 |
rs761500756 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806456 | TTATTGTGTTGATAT[A/G]AACATCTTGGTTAAC | 1130 |
rs761509986 | snp | A/G | 3.35711e-05 | 0.00409688 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777294 | GTAAGTTGTATAAAC[A/G]ACTGAAAGACTTTCC | 1130 |
rs761537042 | snp | A/G | 1.65427e-05 | 0.00287595 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744097 | GTCTGGAAAACTGAG[A/G]TCTTGCTTTGAGTTA | 1130 |
rs761573707 | snp | C/T | 1.65102e-05 | 0.00287312 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830247 | AATTATAGAATTTAG[C/T]TTGGTAAGTAATAGA | 1130 |
rs761583959 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706945 | CTCAGATATGGAGTG[G/T]TCTACTGTAGGTTCT | 1130 |
rs761584784 | snp | C/T | 1.65061e-05 | 0.00287277 | intron-variant | LYST | GRCh38.p7 | 1:235728034 | ATACATTTTTGGAAT[C/T]TGTCTAGATTTATGT | 1130 |
rs761596211 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797182 | GTTCACAGCAGCATT[A/G]TACATAGTAGCAAAA | 1130 |
rs761617429 | snp | A/G | 1.65872e-05 | 0.00287981 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809747 | TTTTAAAGCTGCTCT[A/G]AGCAATTCAGTTAAA | 1130 |
rs761629705 | snp | A/G | 3.42765e-05 | 0.0041397 | intron-variant | LYST | GRCh38.p7 | 1:235752999 | AAGTTTTCCTGTTCT[A/G]AAGTATTTATCAGAT | 1130 |
rs761632662 | snp | C/G | 1.77354e-05 | 0.00297781 | intron-variant | LYST | GRCh38.p7 | 1:235733956 | TTTATTATTTCTCAC[C/G]TAACATTGTCACAGA | 1130 |
rs761634763 | snp | C/T | 1.6517e-05 | 0.00287372 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751162 | AGAACATAGGAAAGT[C/T]AAGCTAGCCTCAATT | 1130 |
rs761636460 | snp | C/T | 1.67871e-05 | 0.00289711 | intron-variant | LYST | GRCh38.p7 | 1:235773835 | AAAAAAAGTACATAT[C/T]ACATGCCTCTGCTTT | 1130 |
rs761656800 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817891 | AAAAATTTGTTACCA[C/G]AAAAATGATCTATTC | 1130 |
rs761663827 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235692579 | AGTAGAGATGGGTTT[C/T]CCCCGTGTTGGCCAG | 1130 |
rs761673454 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235696119 | CACTAAACATAGATA[A/C]AACGGTATGCATCCT | 1130 |
rs761692413 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235782004 | GATGATAAACAATGG[C/T]CAATCATGCAAAATG | 1130 |
rs761692780 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235763737 | GTGCTGGGATTACAG[C/G]ATGAACCACCATGCC | 1130 |
rs761694947 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854026 | GTAAATCATCTCCCC[A/G]GCTTTCTATCCCTGT | 1130 |
rs761717729 | snp | A/T | 3.30475e-05 | 0.00406481 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773945 | TTAAACTCTCCATTC[A/T]CATTCATATAAATAA | 1130 |
rs761724032 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235744795 | GTCACAGCTACTCAG[G/T]AGGCTGAGATGGGAG | 1130 |
rs761731196 | snp | A/G | 1.71519e-05 | 0.00292842 | intron-variant | LYST | GRCh38.p7 | 1:235697045 | TCAAATCTCACGAAA[A/G]ATATATCCAGAATGA | 1130 |
rs761739539 | in-del | -/AT | 1.65184e-05 | 0.00287384 | intron-variant | LYST | GRCh38.p7 | 1:235733700 | AAAGAGACTAAACAA[-/AT]AATAAGATTGTCCAT | 1130 |
rs761739972 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790805 | AATTCTTCAGTTAAA[A/G]AAGGAACTGGAATGA | 1130 |
rs761740124 | snp | C/T | 1.72344e-05 | 0.00293546 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792110 | TAATTTTCAGAATAC[C/T]CAGAAGAAGAATTTT | 1130 |
rs761744796 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235717849 | GAATAGATACAAATT[A/G]ACATCTAAAAACAGA | 1130 |
rs761744885 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819052 | GTGAGTTAGTTCTTG[C/T]AAACCATGGGCCTTG | 1130 |
rs761760512 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875694 | CTACAAAAGTAAAAA[A/G]TTAGCCAGGCATGGT | 1130 |
rs761761594 | snp | A/G | | | missense | LYST | GRCh38.p7 | 1:235697154 | GCTCTGGTGGGCAGA[A/G]CCTGGAGAGAGCCAA | 1130 |
rs761762580 | snp | C/T | 3.31181e-05 | 0.00406914 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762748 | AGCAGTAAAACCAGA[C/T]GGGCTTATTACCATA | 1130 |
rs761769217 | in-del | -/TCAA | | | intron-variant | LYST | GRCh38.p7 | 1:235701628 | CGAGACTCATCTCAA[-/TCAA]TCAATCAATCAATCA | 1130 |
rs761770704 | in-del | -/AGA | 3.29592e-05 | 0.00405938 | intron-variant | LYST | GRCh38.p7 | 1:235693494 | TCTCACACCTCAAGG[-/AGA]AGGAGAAAGAAAAGT | 1130 |
rs761771231 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235849036 | CCAGCATCACACTAA[C/T]ATCAAAACCAGGAAA | 1130 |
rs761778130 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235823892 | CTTCAAAAGCGAAGA[A/G]CTCCTGGTAAAGACA | 1130 |
rs761804787 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788793 | AATACATCCTTCTTC[C/T]ATGAGTCTTTCACCA | 1130 |
rs761837430 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235682393 | AGCTCAACAGGCTGC[C/T]GGCGGACATGGAGAG | 1130 |
rs761857325 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861843 | GGCAAATTCTATTGC[C/T]ACAAATACTATATAA | 1130 |
rs761860625 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235736100 | ATGATTTTCTTAAAC[A/G]CTTAAGTTGTTTCTA | 1130 |
rs761869605 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714830 | AACTGCAATAATGTA[C/T]ATAGGCTCCAAAGGT | 1130 |
rs761887175 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | LYST | GRCh38.p7 | 1:235693433 | TATTATCAGCATATC[C/T]CCAGCTCAGGATGGC | 1130 |
rs761899020 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235678261 | AGGTCGAGACCAGCC[A/T]GGCCAACATGGTGAA | 1130 |
rs761900167 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235731389 | CCCAGTCTCCCAGTT[C/T]CTCGCCTGAAGGCAA | 1130 |
rs761912894 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805858 | GTCTCACTTTCTTGA[C/T]TTGTAAATAGCTTTG | 1130 |
rs761915002 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771537 | AATTTGTTTACATAT[A/G]CTATCCCTGTAATTA | 1130 |
rs761922531 | in-del | -/CTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235732300 | AAACTTTTATGTTTA[-/CTTT]CTTTTTCTTTTTCTT | 1130 |
rs761956888 | snp | C/T | 0.000276927 | 0.0117638 | intron-variant | LYST | GRCh38.p7 | 1:235755679 | AGTCAATTTAGATAA[C/T]GCATTAAAATTAAAT | 1130 |
rs762005849 | snp | A/G | 3.39703e-05 | 0.00412116 | intron-variant | LYST | GRCh38.p7 | 1:235781898 | GTCGCCCAGGCTGAA[A/G]TGCAGTGGTGCAATC | 1130 |
rs762006661 | snp | A/C/G | 4.62955e-05 | 0.00481103 | intron-variant | LYST | GRCh38.p7 | 1:235746536 | CGAGGACCTTTAAAA[A/C/G]TATATAAATTAAAAC | 1130 |
rs762030521 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814523 | AAAGAGAAGTACAAC[C/T]AGAGAAACCAAGGAA | 1130 |
rs762031638 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840833 | TTTCTAAAGCAACAG[C/T]AGAATAATATAATTT | 1130 |
rs762042545 | snp | C/T | 1.65312e-05 | 0.00287495 | intron-variant, splice-acceptor-variant | LYST | GRCh38.p7 | 1:235751379 | TAAAAACAGAAGATA[C/T]TAGAATGTTTTCAAG | 1130 |
rs762042940 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810166 | TTTCCAAAGCCATAG[C/T]ATCTGGAGGAGTCTG | 1130 |
rs762061731 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870449 | TCTGTATGTCACTTT[C/G]CTTTTGCTGTCCATA | 1130 |
rs762068617 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235732084 | TTTTTTTAAAACGTG[A/C]ATCTGTTTTTAATTT | 1130 |
rs762078094 | snp | C/T | 0.00044524 | 0.0149138 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809096 | GTTATGAACACCCGA[C/T]AGGATCTGGACACAA | 1130 |
rs762081502 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703834 | AGTCACAGGGGTTTG[C/T]TGTACAGATGATTTC | 1130 |
rs762087939 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235717139 | GAAAGTTAGTGTCCC[A/C]TTTTCCAGACTCTAC | 1130 |
rs762092603 | snp | A/T | 1.65477e-05 | 0.00287638 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757318 | GCTGGTGATGGGTGG[A/T]TAACGAGGACCAAAA | 1130 |
rs762099794 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741619 | TGGAACCACTGGCTT[C/T]ACTTGAACCCTAAAA | 1130 |
rs762100882 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235672748 | GACTAAGTGTTTTCC[C/T]GTTACCCTATTAAGA | 1130 |
rs762101850 | snp | A/G | 1.65105e-05 | 0.00287315 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809429 | ATGCTCTGAGGCCTC[A/G]GGAGGAACTCCATCT | 1130 |
rs762103744 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859169 | TTCGTTTTTAAACAG[A/G]AAGATACATCATTCC | 1130 |
rs762109784 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235722839 | AATCAGAATTTAACA[C/T]AATTTTGGAGGTCAA | 1130 |
rs762114389 | snp | A/G | 1.6537e-05 | 0.00287545 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801081 | GAAACCTTCTGTTTC[A/G]GACTTTAAGTCTACC | 1130 |
rs762117854 | snp | A/G | 3.30502e-05 | 0.00406497 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759072 | CAAGACTTGGCCAAC[A/G]GCCAACAGCTGCAGA | 1130 |
rs762118926 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841088 | ATTAGGCCAGTGACT[A/T]ACTTCTTTACAGTGA | 1130 |
rs762130174 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702846 | TTCAATATTGAGCTT[C/G]GCTCCAGGTCTGCTC | 1130 |
rs762146710 | snp | C/T | 4.9516e-05 | 0.00497549 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720883 | TTATTTGTGAGTATA[C/T]TGTGGTATACATCAT | 1130 |
rs762147022 | in-del | -/AAGAAGAT | 2.04134e-05 | 0.00319473 | intron-variant | LYST | GRCh38.p7 | 1:235792139 | TCTAGAGAAAAAGAA[-/AAGAAGAT]AAACAAATGAAACTT | 1130 |
rs762148922 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235786020 | TAGGCTAGTCATTCT[-/A]ATTTCTTTTGAAAGC | 1130 |
rs762153468 | snp | C/T | 3.29848e-05 | 0.00406095 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715318 | CGGGAGGCATGGGGT[C/T]ATCTTCTCTGGCTCC | 1130 |
rs762155407 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731109 | AAACGTCTCCTCTCT[C/T]GATTTGGCCCTTCTG | 1130 |
rs762160809 | snp | C/T | 8.29772e-05 | 0.00644063 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806723 | TTAAGCAATTTAATT[C/T]GATTATTTGACTTAC | 1130 |
rs762198115 | in-del | -/AAT | | | intron-variant | LYST | GRCh38.p7 | 1:235688985 | TGAGACTCCGTCTCA[-/AAT]AATAATAATAATAAT | 1130 |
rs762210804 | snp | A/G | 1.6591e-05 | 0.00288015 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788769 | TTTGGATCCCAGTGA[A/G]ATTATATGAATACAT | 1130 |
rs762219500 | in-del | -/T | 3.75848e-05 | 0.00433486 | intron-variant | LYST | GRCh38.p7 | 1:235805698 | GTGTGTGTATATATA[-/T]TGTATATATATTACA | 1130 |
rs762229971 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235752832 | GGGCCAGTTAATAAA[C/G]TAGCATACAGGGACA | 1130 |
rs762235362 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235712899 | CTTTCTAGCCATAGG[A/G]AAAGGCCTAGAATAT | 1130 |
rs762235866 | snp | C/T | 9.90949e-05 | 0.0070383 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809601 | ATCTGAAGAACTCCT[C/T]CCAAAAGCTCAGGTA | 1130 |
rs762240675 | snp | A/T | 1.6528e-05 | 0.00287467 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738638 | TGTCTCCCTCAAGAC[A/T]CTGCACCCAGATTTA | 1130 |
rs762254340 | snp | A/G | 1.7475e-05 | 0.00295588 | intron-variant | LYST | GRCh38.p7 | 1:235813064 | TACATGTCAATGCCT[A/G]TGTCAGTAACAAAAG | 1130 |
rs762254542 | snp | C/G/T | 8.24967e-05 | 0.00642196 | synonymous-codon | LYST | GRCh38.p7 | 1:235677164 | AGGGCTTTTGTGTCC[C/G/T]GCCAGACTTTGTACA | 1130 |
rs762256651 | snp | C/G | 1.65721e-05 | 0.0028785 | missense | LYST | GRCh38.p7 | 1:235664555 | GAACAGATGATCTCC[C/G]TGCAGTGGACATGTC | 1130 |
rs762262644 | snp | A/T | 1.64972e-05 | 0.00287199 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702943 | CGTCTCTGAACTGGA[A/T]CTTCAACTGCAGAGA | 1130 |
rs762290270 | snp | A/C | 8.25471e-05 | 0.00642392 | intron-variant | LYST | GRCh38.p7 | 1:235787400 | GAGAAAAGGCATAGG[A/C]TGAAAACATGAAAAT | 1130 |
rs762307712 | snp | G/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884740 | TTATGGATTTCTGAA[G/T]TAATATTTTTATTTA | 1130 |
rs762308593 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235782913 | TTAATGCTAAGTGAT[C/T]ATGCAGCTTTTGATT | 1130 |
rs762309551 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857533 | AAGCACAAAGAAAGA[A/G]AAATGAGGAGGAGGA | 1130 |
rs762315784 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235820286 | CACCAGATGGCTAGG[A/G]TTCAAGGACTTCTGG | 1130 |
rs762325968 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882911 | ATCAGATTGGAATCT[C/T]TCCAATGAATGTCTT | 1130 |
rs762338683 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847081 | ACATTGTCATGAGGT[C/T]ATCCAAAGTTAAGAT | 1130 |
rs762352507 | in-del | -/TACC | | | intron-variant | LYST | GRCh38.p7 | 1:235768619 | AAAGAAAAAAATTTG[-/TACC]TAGATTTTTTCTAGC | 1130 |
rs762358703 | snp | C/T | 1.74205e-05 | 0.00295127 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808412 | AAAGATCTAGACATG[C/T]TCAACAACCCCCGCC | 1130 |
rs762362348 | snp | C/T | 1.82683e-05 | 0.00302222 | intron-variant | LYST | GRCh38.p7 | 1:235759628 | ATACAAAAATACTAC[C/T]TAAAAATCTATTAAG | 1130 |
rs762388509 | snp | C/T | 1.73252e-05 | 0.00294318 | intron-variant | LYST | GRCh38.p7 | 1:235775113 | AATGGGTGGATATAG[C/T]TTTCTCCCAATTTGC | 1130 |
rs762391090 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235836275 | GAGCTACTAATTTAT[A/G]CACTGAGTTTAGAGC | 1130 |
rs762394378 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768986 | TATCAGATGCCCAGG[A/T]GTGTCAAGTACTGAC | 1130 |
rs762394778 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235783910 | ATTGAGACAGGGTCT[C/T]GCTCTGTCACCCAGG | 1130 |
rs762395112 | snp | C/G | 0.000668025 | 0.0182638 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752070 | AGGTCTTCAATAACC[C/G]TAAAATATTGTGAGC | 1130 |
rs762430643 | in-del | -/AA/AAAAGAA/AAAAGAAAAGAA/AAAAGAAAAGAAAAGAA | | | intron-variant | LYST | GRCh38.p7 | 1:235755428 | AAAAGAAAAGAAAAG[lengthTooLong]AAAAAAGACAAAAGA | 1130 |
rs762432078 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727532 | GAAACAAAAAGCTTA[C/T]TTCTCCTATTACAGG | 1130 |
rs762442807 | snp | A/C | 6.64352e-05 | 0.00576309 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808961 | TCCTAACTGATCCAA[A/C]ATAAGTTTGTTAAGG | 1130 |
rs762449313 | snp | C/T | 1.65195e-05 | 0.00287393 | intron-variant | LYST | GRCh38.p7 | 1:235733719 | TAAGATTGTCCATAG[C/T]TAAGCATACATGGAA | 1130 |
rs762458648 | snp | C/T | 1.74934e-05 | 0.00295743 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780915 | TAAAAAGTTCTCTGA[C/T]TTGTTCACATCGCAA | 1130 |
rs762460421 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235767438 | GTGGCAAAGACTAAG[A/T]CAGGAACATAGATCT | 1130 |
rs762478467 | snp | C/T | 1.6676e-05 | 0.00288751 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775000 | ATTTTCTAATTCATG[C/T]ACTCTTTGTTGGTTG | 1130 |
rs762478549 | snp | A/C | 1.66632e-05 | 0.0028864 | intron-variant | LYST | GRCh38.p7 | 1:235788866 | AGAAAAAGATGTTAG[A/C]ATGATCAGTAAAATG | 1130 |
rs762486146 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235751488 | TGATCAGCATGGGGA[C/T]GATGGTAGTAGACAT | 1130 |
rs762486410 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718908 | TCACTATGACCTTAC[A/G]TTTCTTTTTATTTCC | 1130 |
rs762497229 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235856908 | AGCTGATGGATATAA[-/G]GCAGCTCTTACAAGT | 1130 |
rs762508428 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235794319 | AAATTAGATGACAAG[C/T]AGTGGAAATATTAAA | 1130 |
rs762530871 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872452 | AAAGAGTTTGATCTC[A/G]TGGTAATAGACCGAG | 1130 |
rs762537976 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235710824 | TTGGAACACTTGTCT[G/T]TGGAACCCTGAGTTG | 1130 |
rs762545575 | in-del | -/TATA | | | intron-variant | LYST | GRCh38.p7 | 1:235730614 | GTGTGTGTGTGTGTG[-/TATA]TGTAAACTAACAAGG | 1130 |
rs762561555 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806267 | CTGCTGCTTGGTGCA[C/T]ATGTTCAGGAGAAGG | 1130 |
rs762563479 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759006 | GGTTGTAATTTGGCT[C/T]ATAACCAAGAGAATA | 1130 |
rs762590401 | snp | A/C | 1.65545e-05 | 0.00287697 | intron-variant | LYST | GRCh38.p7 | 1:235746314 | AAATCTGAGGAAAAA[A/C]AAACTAATCCTATAG | 1130 |
rs762593540 | snp | C/G | 9.86631e-05 | 0.00702295 | missense | LYST | GRCh38.p7 | 1:235712180 | GAAAAGTTCTGTCTG[C/G]AATGTCAAAACTTTG | 1130 |
rs762595932 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235774820 | ATTTTCTTCAGGAAT[-/A]ACTGAAATACAAAAC | 1130 |
rs762616676 | snp | C/T | 1.98434e-05 | 0.00314981 | intron-variant | LYST | GRCh38.p7 | 1:235774863 | ACTTTGATGACGAGA[C/T]GAGTATCACTGCATA | 1130 |
rs762627262 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235882210 | AGGAGGAGTTTGGCA[A/G]GCAGGACAAGAGAAA | 1130 |
rs762628708 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673965 | GCAGAGACCCAAATC[A/G]TCCCCTTTCCACTTG | 1130 |
rs762652224 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235737469 | CATACCTAGTCCTTA[C/G]ATTTGTAGTCTCTAA | 1130 |
rs762687293 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733577 | TTTATACATTCCTCT[A/G]ATATGCTGGATCACC | 1130 |
rs762694160 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235666426 | ATTCAGAGAGATAGA[A/C]AGTAAAATAGAGGTT | 1130 |
rs762709179 | snp | A/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235829026 | CTGGTCAACACGGTG[A/T]AACCCCATCTCTACT | 1130 |
rs762709482 | snp | A/C | 1.65982e-05 | 0.00288077 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809902 | CTACTCGACTCTCCA[A/C]GTTGTCGCTCAGACT | 1130 |
rs762719058 | snp | A/T | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746410 | TCCGTTTCAGTTGCT[A/T]GGCTAGGGTTCTCTT | 1130 |
rs762742317 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235720264 | ATGGACCTGATTCAA[C/G]ACAACCAACTATAAA | 1130 |
rs762744969 | snp | A/G | 2.95303e-05 | 0.00384243 | intron-variant | LYST | GRCh38.p7 | 1:235709320 | AAACCTAAAAGAGAA[A/G]ATTAATATTAATATT | 1130 |
rs762750997 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235795504 | GCAAAGACACTATAC[A/G]CCAGCCAAGCCCTAT | 1130 |
rs762771186 | snp | C/G | 3.29603e-05 | 0.00405944 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759356 | GCAGACTCACAGCTA[C/G]TGATGAATGCGTCCT | 1130 |
rs762787116 | snp | C/T | 1.65233e-05 | 0.00287426 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734648 | CAAATACAAAACTAA[C/T]TTGGCTCCATGCTTT | 1130 |
rs762788964 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant | LYST | GRCh38.p7 | 1:235728049 | CTGTCTAGATTTATG[C/T]AAATACAGACTTAAG | 1130 |
rs762791802 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235668393 | TTTAAAAAATTATGT[C/T]CCCTATATACCAAGT | 1130 |
rs762797377 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830325 | CTCCTCCTCTTCTTC[C/T]TCCCTGGCCTCCACC | 1130 |
rs762798400 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817775 | TACCATGCTTATTAC[C/G]TGGGTGATGAAATAG | 1130 |
rs762813007 | snp | G/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759407 | TCGGAACTCCCCAAA[G/T]AATTTTGTTTCTTTG | 1130 |
rs762823279 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235850679 | ACTCAAACAAATCAG[C/T]AGGAAAAAAACAATC | 1130 |
rs762829850 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235721948 | TATAGAGAAAAACAG[A/G]CCAAAGTAAAGGAGG | 1130 |
rs762838397 | in-del | -/GATA | 1.66034e-05 | 0.00288122 | intron-variant | LYST | GRCh38.p7 | 1:235766052 | AGTGGAAATAGCCAT[-/GATA]GATCTAACAAAAATG | 1130 |
rs762839909 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791876 | GCAACGGCAGGTGGA[C/T]TGGGGCTATGTGCCA | 1130 |
rs762844740 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806611 | TTCTGTTCAATGTCT[A/G]TCCCATCAATATCTG | 1130 |
rs762846681 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | LYST | GRCh38.p7 | 1:235804455 | CATCCCACACTTCCG[C/T]CTCTGCTGGTCATAC | 1130 |
rs762857578 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883662 | TTTCGTTTGGTAACG[A/G]GGCTAGGAAATCTCT | 1130 |
rs762866034 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235674709 | AACATAATATTGGCC[A/C]AAAAGGGCGGGGTCT | 1130 |
rs762892929 | snp | A/C | 1.65233e-05 | 0.00287426 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757332 | GTTAACGAGGACCAA[A/C]AGTGTATCTGCTTGA | 1130 |
rs762895241 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831302 | GCCAAGAGGCACAGT[C/G]AAGCTCTGGGCCCCA | 1130 |
rs762902895 | in-del | -/TAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235806804 | GCATGTAAAAAGGTT[-/TAAA]TAAAGAAACATCATT | 1130 |
rs762906561 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705496 | GTTCAAGTGATCCTA[C/T]TGCCTCAGCCTTTTG | 1130 |
rs762907395 | snp | A/C/T | 3.29915e-05 | 0.00406138 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809170 | GGGCACACACTGCAA[A/C/T]GCAACAGCACCGCTC | 1130 |
rs762911368 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235863169 | GGGCCGAGGAGGGCA[G/T]ATGATGAGGTCAGGA | 1130 |
rs762914205 | snp | C/G | 1.65059e-05 | 0.00287275 | intron-variant | LYST | GRCh38.p7 | 1:235728156 | GTAATTGGATATAAG[C/G]GTTTTAAAATGTATG | 1130 |
rs762933661 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235685286 | TTCTGGCTCCTTAAC[A/C]TGCCCTTCTTTGCTT | 1130 |
rs762958384 | snp | C/T | 1.70717e-05 | 0.00292157 | intron-variant | LYST | GRCh38.p7 | 1:235729706 | ATGTTCTGACCAATT[C/T]CAGAGAGGATATGCT | 1130 |
rs762963399 | snp | C/T | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235782025 | ATGCAAAATGTTTTA[C/T]TGCTATCAGATGACA | 1130 |
rs762965409 | snp | A/T | 8.30875e-05 | 0.00644491 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800321 | CAGTTTCAACTTACC[A/T]TGAAAATCAGAATCA | 1130 |
rs762970514 | snp | C/T | 1.6582e-05 | 0.00287936 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744125 | TTACATTTTCTGGAG[C/T]TCTCAAAATGTCAAT | 1130 |
rs762972098 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235864794 | GCCAAGCATGGTGGG[G/T]GATGTGTGCCTGAAG | 1130 |
rs762983595 | snp | C/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885047 | TCCTCCCGCCTTGGC[C/T]TCCCAACTAGCACTT | 1130 |
rs762986997 | snp | A/C | 4.95421e-05 | 0.00497681 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753163 | GAGAAGAAGTAAAAG[A/C]GCATTATGCAAGAGT | 1130 |
rs762991459 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235707150 | CTCATTTGGACTCTA[C/G]TACTACATCCAGGCA | 1130 |
rs763001543 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | LYST | GRCh38.p7 | 1:235731184 | CATACTGCTCTGCAA[A/G]TAAAAAGATTAAAGG | 1130 |
rs763003273 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235692735 | ATACCACAAAAACGT[G/T]TACATGGGCCAGACA | 1130 |
rs763005510 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235721551 | CTTTGCTAAAAACAG[A/G]TATGAAATACCCATT | 1130 |
rs763034311 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235713813 | ATCACTTGAAACTAA[C/T]GAGATGAAAGTGAAT | 1130 |
rs763051527 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235788250 | CTACAACCTCTGCCT[C/T]CCAGATTCAAGTGAT | 1130 |
rs763053467 | snp | A/G | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793559 | TTAGCTCTTCTGAAC[A/G]TGTTCTTGAACTCAT | 1130 |
rs763080785 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235786829 | CCGCATGTTCTCACT[C/T]ATAGGTGGGAATTGA | 1130 |
rs763082080 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235876612 | TTAAATTCTGATTTT[G/T]TGTTCCTGGCAGATC | 1130 |
rs763090410 | in-del | -/AAA | | | intron-variant | LYST | GRCh38.p7 | 1:235849776 | TTTTACAATAGCTCC[-/AAA]AAAAAAAAAAAAAAA | 1130 |
rs763095264 | snp | A/C | 1.66477e-05 | 0.00288506 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716775 | TATAGGTTTAGAGAG[A/C]TTTCTGCAAGAAAAG | 1130 |
rs763139480 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235770120 | TATTATTAAACAACT[A/G]TGGAATATATTTCCA | 1130 |
rs763156837 | snp | A/G | 3.33723e-05 | 0.00408473 | splice-donor-variant | LYST | GRCh38.p7 | 1:235773840 | AAGTACATATTACAT[A/G]CCTCTGCTTTACTCC | 1130 |
rs763157136 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235728272 | GCACTCAATAAATAT[G/T]TTTGAATAGTATCCA | 1130 |
rs763183033 | in-del | -/GAG | 1.65021e-05 | 0.00287241 | intron-variant | LYST | GRCh38.p7 | 1:235730949 | TTGACAACATCTGTT[-/GAG]GAGAAAAGTAAATAT | 1130 |
rs763183850 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235805680 | TTTTTTATATATATA[-/TG]TGTGTGTGTGTATAT | 1130 |
rs763187048 | snp | A/G/T | 3.31896e-05 | 0.00407356 | intron-variant | LYST | GRCh38.p7 | 1:235716672 | GTAAAACAAAACACA[A/G/T]TTTTTCATTTAATAA | 1130 |
rs763192611 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738423 | CAAATCCAGTGGATA[C/T]CTTTGACCTATAGTG | 1130 |
rs763199459 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235876010 | GGTTCACTAGAACCA[-/CT]CAGTAGTTTGAGACC | 1130 |
rs763204819 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235875491 | CTCCAGAGTGGCTGG[G/T]GGAGAGTCTGTTTTA | 1130 |
rs763205903 | snp | A/C | 3.40582e-05 | 0.00412649 | intron-variant | LYST | GRCh38.p7 | 1:235664673 | GTGGCTGTCTCAGAG[A/C]CCACATTTGGCCCCA | 1130 |
rs763207587 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235682263 | CTGGGAGGTTGAGGC[A/T]GCAGTAAGCCGTGAT | 1130 |
rs763209926 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235730616 | GTGTGTGTGTGTGTA[-/TA]TGTAAACTAACAAGG | 1130 |
rs763212916 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773960 | TCATTCATATAAATA[A/G]TATCTTCACCACAGC | 1130 |
rs763216711 | snp | C/T | 8.24137e-05 | 0.00641873 | missense | LYST | GRCh38.p7 | 1:235697181 | CCAAATCTTTCTCCG[C/T]GGGGCTGGCTGAAGC | 1130 |
rs763228956 | in-del | -/GTCTAATCAG | 0.000148752 | 0.00862286 | intron-variant | LYST | GRCh38.p7 | 1:235702701 | CCTGGCATCACAAGA[-/GTCTAATCAG]GTTTTGCTGCACTCG | 1130 |
rs763230913 | snp | C/G | 4.94915e-05 | 0.00497426 | intron-variant | LYST | GRCh38.p7 | 1:235787191 | GCATTTTCTCAAAAT[C/G]CTTCCTACCTCTGTC | 1130 |
rs763232848 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235697665 | AATAGAAATCAAGAC[A/C]ACATGTAGCACAGGA | 1130 |
rs763233556 | snp | C/T | 3.29603e-05 | 0.00405944 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751283 | TGAATCTGTGAGGTT[C/T]TCAGAGTCATGATTT | 1130 |
rs763240124 | snp | A/T | 0.000172512 | 0.00928581 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808419 | TAGACATGCTCAACA[A/T]CCCCCGCCCCCGCCG | 1130 |
rs763244087 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235824711 | ACAAAATGGAGTTTA[C/T]TCCAGGAATGCAAAC | 1130 |
rs763250569 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235756864 | TTTTGAAAAGGTGTC[A/C]TCTAAGCTGAGAGCT | 1130 |
rs763251823 | in-del | -/GATT | | | intron-variant | LYST | GRCh38.p7 | 1:235816234 | ATCACAAGGTCAGGC[-/GATT]GAGACCATCCTGGCA | 1130 |
rs763252439 | snp | A/G | 1.66835e-05 | 0.00288816 | intron-variant | LYST | GRCh38.p7 | 1:235788874 | ATGTTAGAATGATCA[A/G]TAAAATGGTTCGTAA | 1130 |
rs763265353 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837799 | AAACAGCTCTTTTGA[A/G]AAGTTCTGCCACAAA | 1130 |
rs763266566 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842384 | ACAACATCCACAGTG[C/T]GGCCCTGCAAGCAGA | 1130 |
rs763268922 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235797294 | GCCAAAAAAGAAAAG[A/C]AGCAGGGAAGGGGAA | 1130 |
rs763269074 | snp | C/G | 4.96397e-05 | 0.0049817 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741541 | AAATATGCACTAGTA[C/G]TCTCCCAAGCTGCAT | 1130 |
rs763274434 | snp | A/G | | | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715247 | AGGCATCCTGACCAG[A/G]AAGTGAAGCACAGTG | 1130 |
rs763287471 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235759796 | TCTTGCTCTCTTACC[C/T]ACTGAAGTGCAGTGA | 1130 |
rs763289886 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701708 | AGTGACTAAAGTGAT[G/T]TGTGAAGCTTCAAAA | 1130 |
rs763294699 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670798 | TCCAGTGGGGAGGGG[G/T]GTTAAGTCTCCAGGG | 1130 |
rs763295516 | snp | A/C | 1.65993e-05 | 0.00288086 | intron-variant | LYST | GRCh38.p7 | 1:235702981 | TCCAAAATATGTCTG[A/C]AGAGTGAAAGAGTAA | 1130 |
rs763295705 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835006 | TGCAACAACCTCTGC[C/T]GCCTGGGTTCAAGTG | 1130 |
rs763300718 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235755027 | TGCAATGAGCTGAGG[C/T]ATGACTGTGTCTCTC | 1130 |
rs763301720 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684157 | CTTGCAGTATTTAAA[C/T]TGTAATAGCTATGCT | 1130 |
rs763302801 | in-del | -/T | 1.64898e-05 | 0.00287135 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806002 | ATGGTATGGGGTCAC[-/T]TTTTTATAGCCAAAG | 1130 |
rs763346136 | snp | A/T | 1.7856e-05 | 0.00298792 | intron-variant | LYST | GRCh38.p7 | 1:235775133 | TCCCAATTTGCTGAG[A/T]GTAAAAATTTAACAT | 1130 |
rs763360658 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235811912 | AGTTAGTGAATCAAT[A/C]AATAAGCAGAAAAAC | 1130 |
rs763371480 | snp | C/T | 1.65127e-05 | 0.00287334 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808475 | TTTAAGCAGGATAGG[C/T]AGAGTTTTTACATAA | 1130 |
rs763383556 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235702491 | CTGGGAATAACAATT[C/G]TCTCTGCTCCCTGAG | 1130 |
rs763386797 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235856359 | GACTAAAAGTCAAGA[G/T]ATTCTCAGTTTTCTG | 1130 |
rs763391158 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235671954 | TGGACTAGTGTGATA[G/T]ATGTTAGGGTAGGAG | 1130 |
rs763394854 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | LYST | GRCh38.p7 | 1:235731009 | TGCTATATTTATATG[C/T]TGAGTCAAGAAGCCA | 1130 |
rs763428944 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235725390 | GGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 1130 |
rs763432461 | in-del | -/CAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235872295 | AGTGACATTCTGTCT[-/CAAAA]AAAAAAAAAAAAAAA | 1130 |
rs763433116 | in-del | -/AGA | 1.6839e-05 | 0.00290159 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813024 | AGTGGAAGGAGAGAC[-/AGA]AGAAGAGTCAGGAGT | 1130 |
rs763449821 | snp | G/T | 1.64972e-05 | 0.00287199 | intron-variant | LYST | GRCh38.p7 | 1:235752218 | CATTTATAAGAAAAA[G/T]AACAAATAATTTAAG | 1130 |
rs763454873 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235813297 | TTTAGCACACTCCTG[C/T]TGATATTTCCAAAAA | 1130 |
rs763455386 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731137 | CTGTTGGATCCAACT[C/G]CCATGAGGTTGGATA | 1130 |
rs763464758 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235833785 | CACCAATGAAATTTT[G/T]AGATCTTAGGAGCAC | 1130 |
rs763475971 | snp | A/C | 1.64866e-05 | 0.00287106 | missense | LYST | GRCh38.p7 | 1:235677148 | CAGAGACAGCTGTGA[A/C]AGGGCTTTTGTGTCC | 1130 |
rs763478295 | snp | C/T | 3.63135e-05 | 0.00426092 | intron-variant | LYST | GRCh38.p7 | 1:235777032 | AGTAAGTCATTTCTC[C/T]TTAGACAAAACTATA | 1130 |
rs763480268 | snp | C/T | 4.94401e-05 | 0.00497168 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810236 | GTCTTGTTTAGGAAA[C/T]GATGTTAAAAAATGA | 1130 |
rs763486317 | snp | G/T | 2.02263e-05 | 0.00318006 | intron-variant | LYST | GRCh38.p7 | 1:235755690 | ATAATGCATTAAAAT[G/T]AAATATAATATATAC | 1130 |
rs763490025 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756606 | ATCTTTACAAGATTA[C/T]TTTAATATTGGGTTG | 1130 |
rs763494950 | in-del | -/AATGAGAGTAATC | | | intron-variant | LYST | GRCh38.p7 | 1:235783104 | ACTCCATTTTAAGAT[-/AATGAGAGTAATC]TATGAAGGCAAAGTC | 1130 |
rs763515369 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671794 | CGTAGATATGTAAAT[A/G]GGAAGCAATTAGATT | 1130 |
rs763524528 | snp | C/T | 1.66258e-05 | 0.00288316 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762826 | GTACATGATTGACCG[C/T]ACTTTCTCCTGAAAG | 1130 |
rs763532156 | snp | A/G | 1.65652e-05 | 0.0028779 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741559 | TCCCAAGCTGCATTC[A/G]GAAGGTCTCCTTACA | 1130 |
rs763540956 | in-del | -/ATC | | | intron-variant | LYST | GRCh38.p7 | 1:235722860 | TGGAGGTCAAAAATA[-/ATC]ATCATATAACCAAGG | 1130 |
rs763560118 | snp | A/G | 1.65652e-05 | 0.0028779 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809730 | TCTAGGCATATTCTA[A/G]TTTTTAAAGCTGCTC | 1130 |
rs763560832 | snp | A/G | 3.32038e-05 | 0.00407441 | intron-variant | LYST | GRCh38.p7 | 1:235791692 | TCAGATAATCCTGTC[A/G]TCATACCTGTACCAT | 1130 |
rs763563678 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805971 | GTCAGCACTCTTTTT[C/T]AGACTACCTAGTTCT | 1130 |
rs763582673 | in-del | -/AC | | | intron-variant | LYST | GRCh38.p7 | 1:235857747 | CATATGTAAATACAC[-/AC]ACACACACACACACA | 1130 |
rs763604337 | snp | C/T | 3.31334e-05 | 0.00407009 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762785 | GGGCTCATAAGGGAC[C/T]TTCCTCCACTGCTGG | 1130 |
rs763615860 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777123 | CAGAATGCCTTGAAT[A/G]GTTTTATATTCAGTA | 1130 |
rs763726125 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235685675 | ACATGGCGAAACCCT[A/G]TCTCTACTAAAAATA | 1130 |
rs763726975 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | LYST | GRCh38.p7 | 1:235733791 | GTGAAATCTAATGGA[C/T]TCCTAAAATACATGC | 1130 |
rs763730472 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235699265 | CCGCGTGGCCCCAGG[A/G]TGTGTTTTTCCCCTC | 1130 |
rs763733957 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718811 | AATTGCCAAATTTCA[A/T]AGTAAGGAATTGGTG | 1130 |
rs763736405 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727124 | TACTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 1130 |
rs763749796 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777160 | AGATTCTTTAGATGA[C/T]GAGGTTCTAATAAGA | 1130 |
rs763765601 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793288 | AAAATATAATCTCAG[C/T]GATATGTCTGGTTAA | 1130 |
rs763767750 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778397 | TTTATTTTTCCGAGA[C/T]GGAGTCTTGCTCTGT | 1130 |
rs763776382 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868678 | TGTGACTATTATTTT[C/T]TTCGGTACCAGTGTT | 1130 |
rs763779075 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235695791 | GAGCCCGCCACCACG[A/C]CCGGCTAATTTTTTT | 1130 |
rs763779196 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235725310 | GTGATGGCAGGCACC[A/T]GTAGTTCCAGCTACT | 1130 |
rs763781311 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771621 | TTTAGATCTGAAAGT[A/T]TATATTTATTCAGAG | 1130 |
rs763783736 | snp | C/T | 1.66109e-05 | 0.00288187 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808655 | AACAACTATATTGCC[C/T]TTCTGGATTAAATTG | 1130 |
rs763800737 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235737475 | TAGTCCTTAGATTTG[C/T]AGTCTCTAAATACTA | 1130 |
rs763811135 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235714455 | CCCTTTTATAGACCA[A/G]TAAGAGTGAATACAA | 1130 |
rs763811307 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674717 | ATTGGCCAAAAAGGG[C/T]GGGGTCTGTGTCATG | 1130 |
rs763818962 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235686509 | ATGGCTGAAAAATAA[A/T]AAAATTTCTTCCAGT | 1130 |
rs763819881 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235720293 | AAAAGCTATCTTTGA[C/G]AGAAGCAGGGGACAT | 1130 |
rs763826917 | snp | C/G | 4.95962e-05 | 0.00497952 | missense | LYST | GRCh38.p7 | 1:235677188 | TTGTACATAGCATAA[C/G]CTGAAAGAAAAAAGA | 1130 |
rs763833526 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235847950 | TAGTGGGGGACTTCA[A/G]TACTCCAATGACCAG | 1130 |
rs763837950 | snp | A/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806299 | AAGACAAGGCTCTCG[A/T]GAGATATACATGGCA | 1130 |
rs763841237 | snp | C/T | 1.64827e-05 | 0.00287073 | missense | LYST | GRCh38.p7 | 1:235709140 | GCCTTCCCCTTTTGC[C/T]TATACCCAAACACCA | 1130 |
rs763849561 | in-del | -/TGGACT | 0.00400575 | 0.0445739 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791872 | CCCAGCAACGGCAGG[-/TGGACT]GGGGCTATGTGCCAA | 1130 |
rs763867804 | snp | A/G | 6.59924e-05 | 0.00574385 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808508 | CTGAAGCACGTCCTG[A/G]GGCAAGCACTGGTTA | 1130 |
rs763872685 | snp | A/G | 1.65318e-05 | 0.002875 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802990 | TAAAAGTTTAAAACT[A/G]CAACACTGAGAATCC | 1130 |
rs763891209 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235688939 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 1130 |
rs763895163 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235663421 | AAAAATATAACAGTA[C/G]TATATTTTCTCCTTA | 1130 |
rs763897830 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235849013 | CCTACCTAATTCATT[A/G]TATGAAGCCAGCATC | 1130 |
rs763897944 | in-del | -/A | 1.66988e-05 | 0.00288949 | intron-variant | LYST | GRCh38.p7 | 1:235733458 | TAACATCAATATCTT[-/A]AAATCTTCATGGAAG | 1130 |
rs763899390 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705661 | AGAGCATTTGGGTTA[C/T]AGGCATTAGCCACTG | 1130 |
rs763905241 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235694324 | CCAGCCCTCTCTCTT[G/T]TTTACAACATAGTAT | 1130 |
rs763926458 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235755081 | GTGAGACATTGTCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAGC | 1130 |
rs763933686 | snp | A/G | 1.68781e-05 | 0.00290495 | intron-variant | LYST | GRCh38.p7 | 1:235830219 | GTATTTGATATAAAA[A/G]TGTTACCTGATCAAT | 1130 |
rs763959412 | snp | A/C | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661787 | GCCAATAAAGCAGCA[A/C]CCCAAGTAAAAATAT | 1130 |
rs763967050 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235823618 | CATTAGCCAATCCCC[A/G]TTTTACCAAAAGCAA | 1130 |
rs763972274 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770247 | CTGCTGGTGGTGATC[C/T]GCTCTGATGAGGACT | 1130 |
rs763992765 | snp | C/T | 0.00010478 | 0.00723732 | intron-variant | LYST | GRCh38.p7 | 1:235781885 | AAAATCTCACTCTGT[C/T]GCCCAGGCTGAAGTG | 1130 |
rs763994529 | snp | A/G | 1.65789e-05 | 0.0028791 | intron-variant | LYST | GRCh38.p7 | 1:235770122 | TTATTAAACAACTGT[A/G]GAATATATTTCCAAA | 1130 |
rs764016310 | snp | C/G/T | 4.94387e-05 | 0.00497165 | missense | LYST | GRCh38.p7 | 1:235662945 | TCATTCGCATTCACC[C/G/T]GGCTGCATAGCTGCT | 1130 |
rs764017283 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861410 | ATTACTGTAAACAAA[G/T]TTGGGGGATTAAGAG | 1130 |
rs764042499 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785957 | CTCTCCCTGAATCTA[A/T]CACTTGGTATATTTC | 1130 |
rs764046484 | snp | A/G | 1.6659e-05 | 0.00288604 | intron-variant | LYST | GRCh38.p7 | 1:235801114 | TGAAAAGAGAAAAGC[A/G]AAAGATTACTTGTAT | 1130 |
rs764054420 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840200 | AGGCAAATCAATATA[C/T]AGGGTACTATGTACT | 1130 |
rs764059443 | snp | C/G | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724052 | ATCAAATGCCAACAG[C/G]AGTGTTCTGCCATTT | 1130 |
rs764062945 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235673229 | TGTCTCTTTTTTTTT[-/C]CTCTTCTCTTTCCCT | 1130 |
rs764088101 | snp | C/T | 3.30158e-05 | 0.00406286 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809642 | TCTATGACGATACTT[C/T]GAAAACACAAAATCT | 1130 |
rs764104541 | snp | C/T | 1.94158e-05 | 0.00311569 | intron-variant | LYST | GRCh38.p7 | 1:235813112 | GGCGATAAGACACAT[C/T]AGTTCCTAATGTCTT | 1130 |
rs764106931 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860489 | CCTAAAAATCTTCTG[C/T]GCTCTGCGTATTCAT | 1130 |
rs764121832 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235804079 | TCATTTTTATGTTGA[A/C]TGATTTAAAATTAAT | 1130 |
rs764127185 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769466 | CCACCGAAGCAAAGG[C/T]GCTCAAAATATAAAA | 1130 |
rs764135647 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235744757 | AATACAAAAATTAGC[C/T]GGGCATGGGGTGCAC | 1130 |
rs764136984 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235788481 | GCATGAGCCACCACA[A/C]CCAGCCGAGAATTAA | 1130 |
rs764146629 | snp | A/T | 3.4313e-05 | 0.0041419 | intron-variant | LYST | GRCh38.p7 | 1:235733943 | ATACTATATAAAATT[A/T]ATTATTTCTCACCTA | 1130 |
rs764152449 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235695995 | TACTTTGGTATTATT[A/T]GTAAATTACTTGTAA | 1130 |
rs764157793 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant | LYST | GRCh38.p7 | 1:235755457 | GATTCCCAATTATAG[C/T]GGAGGGAAGAACACA | 1130 |
rs764163552 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235701700 | GTAATTACAGTGACT[-/A]AAGTGATTTGTGAAG | 1130 |
rs764167278 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235824748 | AAACTACCGCTGAGC[A/G]CAGTGGCTCACGCCT | 1130 |
rs764179773 | snp | A/G | 1.66988e-05 | 0.00288949 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792081 | TGAAGGGCTCATAGT[A/G]GTATCACTTTCAATA | 1130 |
rs764184574 | snp | G/T | 3.30857e-05 | 0.00406716 | intron-variant | LYST | GRCh38.p7 | 1:235723978 | GAGTATAGTTACAGT[G/T]GCCCATGAGCACTTA | 1130 |
rs764203008 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235874019 | ATAGAATAGAATAAC[A/T]CTTGACCACTTCAAA | 1130 |
rs764206410 | snp | A/T | 1.65767e-05 | 0.00287891 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808992 | ATATTCAATATATGC[A/T]GCTGAAAATTTTTCA | 1130 |
rs764207947 | snp | G/T | 8.23757e-05 | 0.00641725 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791976 | TCTCAATAAACCCAT[G/T]GCCTTACTGTTTAAA | 1130 |
rs764211462 | snp | C/T | 3.31142e-05 | 0.00406891 | intron-variant | LYST | GRCh38.p7 | 1:235730814 | GCTGTTGTATATTCA[C/T]GAAAGAGTGAAGGTC | 1130 |
rs764216403 | snp | C/T | 3.33539e-05 | 0.00408361 | intron-variant | LYST | GRCh38.p7 | 1:235715368 | AAGTACTGAAAGAAA[C/T]GGTGAATCCAGAGAA | 1130 |
rs764217919 | snp | C/T | 1.77398e-05 | 0.00297818 | intron-variant | LYST | GRCh38.p7 | 1:235759614 | CCTGGTAAGAGTAGA[C/T]ACAAAAATACTACTT | 1130 |
rs764221345 | snp | A/G | 0.00018152 | 0.00952507 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810081 | TTCATGTTACTGATA[A/G]CAGACAAGGCAGCTG | 1130 |
rs764243780 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235775621 | GACAATAGGTATTCT[-/G]GAGAGCACAGAGACC | 1130 |
rs764270411 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235669930 | GGGGTGGGGATTGAC[C/T]TATGTAACAAAACCT | 1130 |
rs764277268 | snp | C/G | 1.65759e-05 | 0.00287883 | missense | LYST | GRCh38.p7 | 1:235664545 | GAAAGCCACGGAACA[C/G]ATGATCTCCCTGCAG | 1130 |
rs764287138 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872879 | CGAGATCCCACCATC[A/G]CACTCCAGCCTGGGT | 1130 |
rs764294963 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235731986 | AAAACATATTAAGTA[A/C]ATTTTTAGAAATAAA | 1130 |
rs764297168 | snp | A/G | 3.30868e-05 | 0.00406723 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738622 | AAGCAAATGTTACTG[A/G]TGTCTCCCTCAAGAC | 1130 |
rs764299046 | snp | A/G | 1.67433e-05 | 0.00289333 | intron-variant | LYST | GRCh38.p7 | 1:235729548 | AATAATCTAAGAATC[A/G]AATAAGGCAGGGTGA | 1130 |
rs764303767 | snp | A/G | 3.76485e-05 | 0.00433853 | intron-variant | LYST | GRCh38.p7 | 1:235805696 | TGTGTGTGTGTATAT[A/G]TATGTATATATATTA | 1130 |
rs764306146 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866488 | ATAAAGGTAGCAACA[C/T]ACCGCCGTCAGCCTG | 1130 |
rs764307854 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764981 | CATTCTTGTCCTACC[C/T]TCCAACTAGTAATAC | 1130 |
rs764330548 | in-del | -/ATCAA | | | intron-variant | LYST | GRCh38.p7 | 1:235860772 | ACCCATGAAACCATC[-/ATCAA]ATCAAGATAGTAAAC | 1130 |
rs764334824 | snp | A/T | 1.64985e-05 | 0.0028721 | intron-variant | LYST | GRCh38.p7 | 1:235787391 | ACAGAAAAAGAGAAA[A/T]GGCATAGGCTGAAAA | 1130 |
rs764356778 | snp | A/C/T | 8.27227e-05 | 0.00643084 | intron-variant | LYST | GRCh38.p7 | 1:235687066 | TGAAAAAGGACCAAT[A/C/T]AAAGATTATCATGTT | 1130 |
rs764366661 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670808 | AGGGGGGTTAAGTCT[C/T]CAGGGAAAGGGTGCA | 1130 |
rs764368579 | snp | C/T | 1.70281e-05 | 0.00291783 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780962 | TATTTGGAGTAGTCA[C/T]TGACTGGCTTGCCAT | 1130 |
rs764380427 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235852481 | TTGCCGGACCTTTTT[C/G]CCGGGGAAGTCTCAC | 1130 |
rs764390767 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720716 | CGTAGTCAGCAAGTA[C/T]AAATGGGAACACAGG | 1130 |
rs764396597 | snp | A/C | 1.65141e-05 | 0.00287346 | synonymous-codon | LYST | GRCh38.p7 | 1:235697225 | TGGAGCACTGGGGGA[A/C]CCCACGTATTCCCCC | 1130 |
rs764415532 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810162 | GAATTTTCCAAAGCC[A/G]TAGCATCTGGAGGAG | 1130 |
rs764434504 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235796024 | AAATTAAATAAAAGG[C/T]TGGGATTGAAAAAAT | 1130 |
rs764453675 | snp | C/T | 3.29957e-05 | 0.00406162 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804611 | GTGTTTCAATCACCT[C/T]TGACTGGGAAAGATG | 1130 |
rs764455726 | snp | A/T | 1.83572e-05 | 0.00302957 | intron-variant | LYST | GRCh38.p7 | 1:235774905 | GAATAAATTTTATGA[A/T]GACATACCTTCAAAA | 1130 |
rs764470376 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235689161 | TTCTCATCCAGTTTA[C/G]TCATTTGACTCAAAG | 1130 |
rs764471809 | snp | C/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854740 | ATTAGATATTATCAT[C/G]ATCACCTTGAATCTG | 1130 |
rs764492828 | snp | C/T | 3.29755e-05 | 0.00406038 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809310 | TGAGAATATTCACAT[C/T]GTCTGTGCCTTTTTC | 1130 |
rs764493178 | in-del | -/AAGTGGTCGTCCCACCTGGGAAGGCCTCCCA | | | intron-variant | LYST | GRCh38.p7 | 1:235680496 | CAAACTCTTGGCTTC[lengthTooLong]AAGTGCTGGGATTAC | 1130 |
rs764511909 | in-del | -/AACTT | 5.33433e-05 | 0.00516418 | intron-variant | LYST | GRCh38.p7 | 1:235766321 | ATTTAAAGAATTGTC[-/AACTT]AACTAAGATTTTTCA | 1130 |
rs764522964 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235782808 | TATGTCATCTATGAG[C/G]CCTTTGAAAACTAAT | 1130 |
rs764524095 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235695119 | AACACTGACCTCTCC[-/C]AGACCCTAGGGTATT | 1130 |
rs764528497 | snp | A/T | 1.66067e-05 | 0.00288151 | intron-variant | LYST | GRCh38.p7 | 1:235757493 | AGTCTTACTAACATG[A/T]CAAGAAAAGTACTTG | 1130 |
rs764531464 | snp | A/G | 1.65364e-05 | 0.0028754 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806711 | TTCGAATACCATTTA[A/G]GCAATTTAATTCGAT | 1130 |
rs764555650 | snp | C/T | 1.65113e-05 | 0.00287322 | splice-acceptor-variant, missense, intron-variant | LYST | GRCh38.p7 | 1:235751363 | GTGCAACAGCCATAT[C/T]TAAAAACAGAAGATA | 1130 |
rs764563948 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235880435 | TGTTGATTTATTACT[C/T]GGTAAAAGTGTCATC | 1130 |
rs764573401 | snp | G/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235740001 | AACACCGCAGTTGAA[G/T]TTTGATGGATAGCAA | 1130 |
rs764574136 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235812074 | AAGGGTCAAGAGGAA[A/C]ACTATTAATCTCTCC | 1130 |
rs764575899 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235876766 | GCTAATTTGAGAGGC[A/C]CAGTCCTGTCATATA | 1130 |
rs764577431 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787257 | CTTTTCCCTTGGGGC[G/T]GCTGTAAGTAGGTGA | 1130 |
rs764592920 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702751 | AAATGACATACCGGA[C/T]AGGTGATTTCTTTGA | 1130 |
rs764594333 | in-del | -/CACT | | | intron-variant | LYST | GRCh38.p7 | 1:235882047 | ATATTTAAACACACA[-/CACT]CACACATACACACAC | 1130 |
rs764617457 | snp | G/T | 1.65059e-05 | 0.00287275 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809424 | TTCAAATGCTCTGAG[G/T]CCTCGGGAGGAACTC | 1130 |
rs764622032 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235798888 | AGGGTTTCTTTTGGG[A/G]GTGATGAAAATGTTC | 1130 |
rs764626850 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235882389 | CCTGTGTGCCATGCG[A/G]AAGCTTTGGACTTTA | 1130 |
rs764661435 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845469 | TCTAACAATTTGAAC[A/G]CGGTGAGAAGCCTGC | 1130 |
rs764672786 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764792 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCCCATT | 1130 |
rs764681844 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235837624 | AGTGAGACCCTGTTT[-/C]AAAAAAAAAAAAAAA | 1130 |
rs764685877 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235791277 | CAAGAGTGAAACTGT[-/C]CTCAAAAAAAAAGAG | 1130 |
rs764689371 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235703774 | TTTTAAAAAAACCTT[C/T]AGGTTCAGCAGTACA | 1130 |
rs764697537 | snp | C/T | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724110 | CTCAATTGCCACCAA[C/T]GCTTGTGAACTTCTT | 1130 |
rs764739538 | snp | G/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777182 | CTAATAAGATGCTCT[G/T]AACTTCTTTTGAGCT | 1130 |
rs764742292 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235744906 | TCAAAAAAAAAAAGA[-/A]AAAAAAAAAGAGAGA | 1130 |
rs764744548 | snp | A/C | 2.23901e-05 | 0.00334583 | intron-variant | LYST | GRCh38.p7 | 1:235734692 | ATTTTTTAGTCATTT[A/C]GAATTTTAATTCTTA | 1130 |
rs764774318 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235747592 | CAAGAGTTTTACTGT[C/T]AAACAATATACTTAG | 1130 |
rs764783720 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235725237 | TCAGGAGTTCAAGAC[C/T]AGCTTGGCCAACATG | 1130 |
rs764821485 | snp | C/T | 6.66489e-05 | 0.00577235 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744002 | CTTTGAATCCTTCTA[C/T]CAGATATGTAAAAAT | 1130 |
rs764843145 | snp | A/G | 8.25035e-05 | 0.00642222 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757409 | GAAGAACCCCACTTA[A/G]GAGTTCATATAATCC | 1130 |
rs764844287 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235674847 | GCCGAAAAGTCATAG[A/C]AAAATGGTTTAGAAA | 1130 |
rs764852763 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857137 | TTTTTAGTAGAGATG[C/G]GGTTTCACCATGTTG | 1130 |
rs764855734 | snp | C/T | 6.61015e-05 | 0.0057486 | intron-variant | LYST | GRCh38.p7 | 1:235731213 | GGGTGTTTTAAGTGA[C/T]CATCCAGGACTTGTA | 1130 |
rs764859050 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235746229 | ATGGATGTTAAGAAC[C/T]GAAAAATAATGCTGC | 1130 |
rs764859264 | snp | G/T | 1.65575e-05 | 0.00287724 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753134 | GCTACCTTAGAACAA[G/T]AATTTAAAATTTGGA | 1130 |
rs764878449 | snp | C/G | 1.65083e-05 | 0.00287296 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806182 | CATACTCGGAAACCA[C/G]CAAGCCTATAAAACT | 1130 |
rs764879928 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724120 | ACCAACGCTTGTGAA[C/T]TTCTTTAATTTCTTC | 1130 |
rs764890533 | in-del | -/TTCT | | | intron-variant | LYST | GRCh38.p7 | 1:235666081 | ACATATAAACAATGC[-/TTCT]TTATTTAAAAATATG | 1130 |
rs764909103 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733568 | CAAATCTACTTTATA[C/T]ATTCCTCTAATATGC | 1130 |
rs764910724 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235794147 | CAGCATGAGCTCACT[C/T]TTCTTGAAGATTAAT | 1130 |
rs764911546 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235698517 | TGAAAACAAGCTTCT[A/C]AAATTTTGTCTAACA | 1130 |
rs764912339 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235743159 | CATAGAGTATTCCCT[A/G]ACAATTAACCAATTG | 1130 |
rs764914278 | snp | A/G | 4.99604e-05 | 0.00499777 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800368 | TCAAGAACCCTCCTA[A/G]AAGATTTTTCACAGT | 1130 |
rs764936561 | in-del | -/TGTGTGTGTGTGTGTGTATA | | | intron-variant | LYST | GRCh38.p7 | 1:235730598 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTATA]TGTAAACTAACAAGG | 1130 |
rs764937291 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235828793 | AAATAAATCACTATA[C/T]ATGGTCTAACATGAT | 1130 |
rs764938143 | snp | C/G | 1.66316e-05 | 0.00288367 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810488 | TTGTGAACTTGAGTT[C/G]TTTTCTTTGGTCAGG | 1130 |
rs764943418 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235686293 | AATTGATTGAGCCCG[G/T]GAGGCAGAGGTTGCA | 1130 |
rs764952823 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734519 | GTCTGCTTTTGTTGA[C/T]GCACTGGGAGGGATG | 1130 |
rs764957880 | snp | C/G/T | 3.34853e-05 | 0.00409167 | intron-variant | LYST | GRCh38.p7 | 1:235773837 | AAAAAGTACATATTA[C/G/T]ATGCCTCTGCTTTAC | 1130 |
rs764963154 | snp | A/G | 1.64991e-05 | 0.00287215 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830253 | AGAATTTAGCTTGGT[A/G]AGTAATAGAAATCCT | 1130 |
rs764965108 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735972 | GTGTCTTAAAGGTAA[C/T]GATCTTGATATAACT | 1130 |
rs764966465 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235792601 | ATTACAGGCGTGAGT[C/T]ACCATGCCCAGCCTT | 1130 |
rs764978673 | snp | A/T | 9.8868e-05 | 0.00703024 | missense | LYST | GRCh38.p7 | 1:235662953 | ATTCACCCGGCTGCA[A/T]AGCTGCTAAGGAAGG | 1130 |
rs764984925 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235718701 | TTTTTCATATTAAAC[A/G]AACAAAATATTCCCT | 1130 |
rs764986307 | in-del | -/TATGTGTGTGTGTGTGTG | | | intron-variant | LYST | GRCh38.p7 | 1:235730566 | ATATATACATATTTA[-/TATGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 1130 |
rs764991912 | snp | G/T | 3.29832e-05 | 0.00406085 | missense | LYST | GRCh38.p7 | 1:235677573 | CTGGTTATCTCTTCT[G/T]TGTGACCATAGAGAT | 1130 |
rs764992684 | snp | C/T | 1.84927e-05 | 0.00304072 | intron-variant | LYST | GRCh38.p7 | 1:235791600 | AAGGTGAAGAACATG[C/T]TAAGAGTGTTAAGAA | 1130 |
rs765001761 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235774630 | ATCAATCTACAGAAT[C/G]AAGGGACAGCATGGG | 1130 |
rs765006632 | snp | A/C/G | 3.30231e-05 | 0.00406333 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806095 | TTTACACTTGTATCT[A/C/G]CCTCCTTTTTTCCTT | 1130 |
rs765011284 | snp | A/G | 1.65444e-05 | 0.00287609 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802957 | TTCACTATCTGCTTC[A/G]TAACCTTCTTCTTCA | 1130 |
rs765019078 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673000 | AACCCGGAGATCACA[C/T]CCTTATCAGAAGTTG | 1130 |
rs765027901 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235814887 | CCTCTGCCACACATG[A/C]GCCCTCCGCATACAT | 1130 |
rs765036798 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235717418 | CATTCTGTGAACACC[A/G]CATGACACCATTCCT | 1130 |
rs765043627 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235765313 | AGTTCCACTGTTACT[A/C]TGCCCAGATTCTGTT | 1130 |
rs765047701 | snp | A/G | 1.77281e-05 | 0.00297721 | intron-variant | LYST | GRCh38.p7 | 1:235733958 | TATTATTTCTCACCT[A/G]ACATTGTCACAGAGC | 1130 |
rs765049166 | in-del | -/AAAAAAAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235816133 | AGACTCCATCTCAAA[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 1130 |
rs765059203 | snp | A/G | 1.67953e-05 | 0.00289782 | intron-variant | LYST | GRCh38.p7 | 1:235803100 | AAGGTTGTAACATTT[A/G]CTTGTTTTTAGTAAT | 1130 |
rs765076933 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235704309 | ATAGTAGTTCTGTTT[C/T]TAGCTCTCTGAGGAA | 1130 |
rs765087143 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235742319 | AATTGGCTGGGTGTG[A/G]TGGTGGGTGCCTGTA | 1130 |
rs765092002 | snp | A/G | 1.81237e-05 | 0.00301023 | intron-variant | LYST | GRCh38.p7 | 1:235773803 | TGTTATATGCATTTT[A/G]CCACAATAAAAAATG | 1130 |
rs765098921 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235797185 | CACAGCAGCATTATA[C/T]ATAGTAGCAAAAAAG | 1130 |
rs765106887 | snp | A/C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673931 | TAAAAGCGATTGTTG[A/C/T]GCTTTTGCAACAGGC | 1130 |
rs765118069 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866503 | CACCGCCGTCAGCCT[A/G]CTCGACCTCGCCCCC | 1130 |
rs765123057 | snp | G/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759209 | TCCCCAGGACTGTCA[G/T]CTTCTGACCTGGGTT | 1130 |
rs765160019 | in-del | -/AGA | 0.000380344 | 0.013785 | cds-indel, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753149 | GAATTTAAAATTTGG[-/AGA]AGAAGTAAAAGAGCA | 1130 |
rs765167682 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235850458 | AAACCTTTCTAGACA[C/T]TGGCTTAGGCAAGGA | 1130 |
rs765168603 | in-del | -/C | 1.65192e-05 | 0.00287391 | intron-variant | LYST | GRCh38.p7 | 1:235733712 | AAATAATAAGATTGT[-/C]CCATAGTTAAGCATA | 1130 |
rs765181955 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235775963 | ATACTTTAAAAGTCT[C/T]ATTGGCAAGATACTA | 1130 |
rs765192422 | snp | A/C | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806457 | TATTGTGTTGATATG[A/C]ACATCTTGGTTAACA | 1130 |
rs765210466 | snp | A/G | 1.64982e-05 | 0.00287208 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808528 | AGCACTGGTTATGAT[A/G]GCTACATACATGACT | 1130 |
rs765240247 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755543 | TAACAATTCTTGAGT[C/T]CCTCGATGAAGATAC | 1130 |
rs765251187 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235816808 | AATACCATCCTGGAC[A/G]TAGGCCCTGGCAAAG | 1130 |
rs765255604 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235849046 | ACTAATATCAAAACC[A/G]GGAAAGGACATAACC | 1130 |
rs765268083 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235760526 | TAGTGCATGGGATAC[A/G]AGTGCATGCCATTCA | 1130 |
rs765278943 | snp | A/G | 0.00023183 | 0.0107639 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793538 | GAAATATTCTCAAAA[A/G]AAGGGTTAGCTCTTC | 1130 |
rs765282594 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235784521 | GCATAGGGTTTTAAA[A/G]CATGGGCCCTCCCTA | 1130 |
rs765283781 | snp | C/T | 3.30044e-05 | 0.00406216 | intron-variant | LYST | GRCh38.p7 | 1:235728039 | TTTTTGGAATCTGTC[C/T]AGATTTATGTAAATA | 1130 |
rs765285216 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235744669 | CTGTGGGAGGTGAAA[A/G]CACACAGATCACCTG | 1130 |
rs765293275 | snp | A/G | 1.65441e-05 | 0.00287607 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746463 | CACATGAAGCTCATC[A/G]TTTGCCACTGAACGC | 1130 |
rs765300265 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235705449 | GGAATGCAGTGGCAC[A/G]ATCATGGCTCACTGC | 1130 |
rs765300935 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235714934 | AATTTTATGGTTTGT[A/G]AATTATATCTTAATT | 1130 |
rs765302634 | snp | G/T | 1.88468e-05 | 0.0030697 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753047 | TTTTAAACTTACTTC[G/T]TTTCTAATCCATTCA | 1130 |
rs765308485 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235743392 | CCAAAATCTAGTTTA[A/G]ATTTAGAGATTGACA | 1130 |
rs765317185 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759335 | TCCATTTCACAAACA[C/G]TTTTTGCAGACTCAC | 1130 |
rs765326576 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235781271 | TGTATATAAAGTTAA[A/T]TGTGAAGCTTTTAAT | 1130 |
rs765327013 | snp | G/T | 5.09031e-05 | 0.0050447 | intron-variant | LYST | GRCh38.p7 | 1:235781899 | TCGCCCAGGCTGAAG[G/T]GCAGTGGTGCAATCA | 1130 |
rs765327140 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693595 | TAGCAGAACATATCA[-/T]TTGGTGCAAGACCAT | 1130 |
rs765338918 | snp | G/T | 1.65751e-05 | 0.00287876 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733905 | TCATATTTCTTTTGT[G/T]CCTAGAAGATTTAGA | 1130 |
rs765349035 | snp | C/T | 1.74418e-05 | 0.00295307 | intron-variant | LYST | GRCh38.p7 | 1:235755681 | TCAATTTAGATAATG[C/T]ATTAAAATTAAATAT | 1130 |
rs765355844 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715330 | GGTCATCTTCTCTGG[C/T]TCCTTTGCGGTACTC | 1130 |
rs765358506 | snp | A/G | 1.737e-05 | 0.00294698 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792113 | TTTTCAGAATACCCA[A/G]AAGAAGAATTTTCTA | 1130 |
rs765360919 | snp | C/T | 1.70854e-05 | 0.00292274 | intron-variant | LYST | GRCh38.p7 | 1:235697049 | ATCTCACGAAAGATA[C/T]ATCCAGAATGATCTT | 1130 |
rs765363830 | snp | C/T | 4.9675e-05 | 0.00498348 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762756 | AACCAGATGGGCTTA[C/T]TACCATAAATCCAGG | 1130 |
rs765369584 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235704088 | AAAGGACATGATCTT[C/G]TTCTTTTTTATGGCT | 1130 |
rs765370714 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785753 | CTTAATCCTCTACCA[C/T]GCTACATTACAGTTT | 1130 |
rs765375287 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840841 | GCAACAGTAGAATAA[C/T]ATAATTTTATTAAAT | 1130 |
rs765375461 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702151 | ATGCTGTTTTTATAA[C/T]GAAGAATTGAGTTGA | 1130 |
rs765382135 | in-del | -/TTAT | | | intron-variant | LYST | GRCh38.p7 | 1:235778367 | CTTAGATTATTCTTA[-/TTAT]TTATTTATTTATTTA | 1130 |
rs765382234 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235875776 | TTGAGCCCAGGAGTT[C/T]GAGGCTTGCAGTGAG | 1130 |
rs765387806 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769438 | GCCCAACTATAATGA[A/G]AAGCCCTTAGTGCCA | 1130 |
rs765410057 | snp | C/G | 0.000164785 | 0.00907555 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810232 | GGTGGTCTTGTTTAG[C/G]AAACGATGTTAAAAA | 1130 |
rs765410792 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235836665 | CTAAAGTAAGCATGG[A/G]AAGAGGAAATAGAAG | 1130 |
rs765415131 | snp | A/G | | | stop-gained, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808519 | CCTGAGGCAAGCACT[A/G]GTTATGATGGCTACA | 1130 |
rs765429563 | in-del | -/TTT | | | intron-variant | LYST | GRCh38.p7 | 1:235695631 | TTACAGTACTCTAAT[-/TTT]TTTTTTTTTTTTTTT | 1130 |
rs765429680 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235732393 | CTGTAGCCTTGAACT[C/G]CTGGGCTCAAGTGAT | 1130 |
rs765435015 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235694120 | GTTCAGGTGATTCTC[A/G]TGCCTCAGCCTCCCC | 1130 |
rs765439131 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235679652 | CCAGATGACACCCAC[C/T]ACCACACCAGCCTGG | 1130 |
rs765448746 | snp | C/T | 1.65105e-05 | 0.00287315 | synonymous-codon, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770277 | TTCTAGAGCTGCTAG[C/T]AAAGTTTCCCAAACA | 1130 |
rs765453860 | snp | A/G | 1.67005e-05 | 0.00288963 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752072 | GTCTTCAATAACCCT[A/G]AAATATTGTGAGCCT | 1130 |
rs765464019 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854664 | ATATCAACATTAAAC[A/G]AGATAATTCATGTAA | 1130 |
rs765472385 | in-del | -/G | 6.73593e-05 | 0.00580303 | intron-variant | LYST | GRCh38.p7 | 1:235805719 | ATATATTACATAAGA[-/G]TTGGACTAAGGACAA | 1130 |
rs765504780 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | LYST | GRCh38.p7 | 1:235693449 | CCAGCTCAGGATGGC[C/T]GACCACTGAATGTCC | 1130 |
rs765507530 | in-del | -/TAAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235812613 | ATAGAAAGCAGTCTT[-/TAAAA]TAAGCAAAGAAACTT | 1130 |
rs765507621 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837829 | AGCATGCAAGGGAAC[A/G]GGTGATGGCTTGAGG | 1130 |
rs765530829 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235699470 | TATTTTCTTTATCTA[C/G]TCTATCATTGATGGG | 1130 |
rs765542937 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702851 | TATTGAGCTTGGCTC[C/T]AGGTCTGCTCACATG | 1130 |
rs765542988 | snp | A/T | 1.68244e-05 | 0.00290033 | intron-variant | LYST | GRCh38.p7 | 1:235664426 | ACTCCTGTGTCCTTA[A/T]GAATGAAATCAAAAA | 1130 |
rs765560595 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235841132 | ATCCACCATGCCTTT[-/C]ATTCCAATTTCAGCA | 1130 |
rs765565075 | snp | C/T | 3.48535e-05 | 0.00417439 | intron-variant | LYST | GRCh38.p7 | 1:235715408 | GTGGGCTCCAGGCAA[C/T]GCTAGAAAAGTGCTG | 1130 |
rs765570115 | snp | A/C | 1.6582e-05 | 0.00287936 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741382 | AGACTTTGTATTTCA[A/C]CAAACGTTTTACTTC | 1130 |
rs765582276 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235839242 | ATATGTGTGGGTGTA[C/T]GTGTGCATATATATA | 1130 |
rs765594619 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235769995 | CTGTAAGATGCAGCA[C/G]TTGAAAAACTCCTGT | 1130 |
rs765597696 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823101 | GAACATGGTCTGTTA[C/T]ACCACAATCAACTGA | 1130 |
rs765612983 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235733452 | TTCCGTTTAACATCA[A/G]TATCTTAAATCTTCA | 1130 |
rs765617842 | snp | C/T | 3.76364e-05 | 0.00433783 | intron-variant | LYST | GRCh38.p7 | 1:235759639 | CTACTTAAAAATCTA[C/T]TAAGTGGAACCACCT | 1130 |
rs765623825 | snp | A/C | 1.64887e-05 | 0.00287125 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810113 | CTCACTTAAAATGTC[A/C]GTGTTTGACCCCTGT | 1130 |
rs765652279 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756168 | ATCTTAAATGCAACA[C/T]GTGTAATACCAAATT | 1130 |
rs765667505 | snp | C/T | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805866 | TTCTTGACTTGTAAA[C/T]AGCTTTGCTTCCTCG | 1130 |
rs765668775 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853624 | CAATAAACAACATTG[C/T]CTATTTCGCTACCCC | 1130 |
rs765674829 | snp | C/T | 1.69513e-05 | 0.00291125 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806749 | CTTACTCCATTACAA[C/T]TCAAAAACAAATCTC | 1130 |
rs765682793 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235754795 | GACAAAAGACCTTGC[C/T]GGGTGTGGTGGCCCA | 1130 |
rs765683522 | snp | C/G | 0.000195293 | 0.00987971 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853108 | CACCACAAACTTCTT[C/G]CCCCCCCACAAACTT | 1130 |
rs765698199 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235701640 | TCAATCAATCAATCA[A/C]TCAATCAATCAAGTG | 1130 |
rs765718043 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235783469 | GGAACATCACACACC[A/G]GGGCCTGTCGGCGGG | 1130 |
rs765720380 | snp | C/T | 3.30868e-05 | 0.00406723 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741529 | GGGCTGGCGACAAAA[C/T]ATGCACTAGTAGTCT | 1130 |
rs765742303 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235687935 | GCTTCCCCCCTTGCA[C/T]TACAAGTGTGTTCAC | 1130 |
rs765743164 | snp | A/G | 1.65696e-05 | 0.00287828 | synonymous-codon | LYST | GRCh38.p7 | 1:235664566 | CTCCCTGCAGTGGAC[A/G]TGTCCAACGAGATCC | 1130 |
rs765746561 | in-del | -/CAT | 0.000143693 | 0.008475 | intron-variant | LYST | GRCh38.p7 | 1:235792175 | TCACGTAATAAAGTA[-/CAT]AATAATCTTGAAATT | 1130 |
rs765750967 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733589 | TCTAATATGCTGGAT[C/T]ACCTTTTTTCTCTCA | 1130 |
rs765751610 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235779176 | CTGGCCGAGGGTACC[A/C]CTTCTCCCTAACCAT | 1130 |
rs765757500 | snp | A/T | 1.71944e-05 | 0.00293205 | intron-variant | LYST | GRCh38.p7 | 1:235805713 | ATGTATATATATTAC[A/T]TAAGAGTTGGACTAA | 1130 |
rs765757966 | snp | C/G/T | 3.45246e-05 | 0.00415467 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235774928 | CTTCAAAATGTAAAA[C/G/T]CCAACAATGCATTTT | 1130 |
rs765776422 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235811546 | ATAGGGCCTGGCGTA[C/T]GGTCAACACTCAGTA | 1130 |
rs765805285 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | LYST | GRCh38.p7 | 1:235731005 | TCTCTGCTATATTTA[C/T]ATGTTGAGTCAAGAA | 1130 |
rs765810040 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235675762 | TGAGTCATTCTAGCA[A/C]ATTATTGAACCTGAG | 1130 |
rs765817484 | snp | C/G | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866713 | CCCTCGCGCCCTCAG[C/G]CCGGCGGTCCCGGCC | 1130 |
rs765818350 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718998 | CAGCGAGAGGCACTT[A/C]AAGTTGGCTTCTGAG | 1130 |
rs765831508 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738579 | GTCCTTGGGGAACAT[A/G]GAGATTCTAGTGTGC | 1130 |
rs765837584 | snp | A/T | 1.64817e-05 | 0.00287064 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810168 | TCCAAAGCCATAGCA[A/T]CTGGAGGAGTCTGTT | 1130 |
rs765872455 | snp | A/T | 1.66452e-05 | 0.00288484 | intron-variant | LYST | GRCh38.p7 | 1:235757503 | ACATGACAAGAAAAG[A/T]ACTTGATGATTACCT | 1130 |
rs765883168 | in-del | -/AAGA | | | intron-variant | LYST | GRCh38.p7 | 1:235830704 | ACATTTTCTCTTTTT[-/AAGA]GAGAAGACTTTCTTT | 1130 |
rs765898748 | snp | A/T | 1.65378e-05 | 0.00287552 | intron-variant | LYST | GRCh38.p7 | 1:235730832 | AAGAGTGAAGGTCTA[A/T]TGATTCAAAGTTACC | 1130 |
rs765908017 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235833367 | TATATATCCTTTTGT[A/G]ACTTTGCTTTTTCCT | 1130 |
rs765914894 | snp | A/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865505 | TAAATATTTACTAAA[A/T]ACATATATATAATTA | 1130 |
rs765927695 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235764477 | TATTCATTTACTACA[A/T]TTCTTTTTTTTTCTT | 1130 |
rs765939688 | snp | A/C | 1.67335e-05 | 0.00289248 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810511 | TGGTCAGGATTATAT[A/C]TGCTGAGAGCGGTAG | 1130 |
rs765942825 | snp | C/T | 3.31466e-05 | 0.0040709 | intron-variant | LYST | GRCh38.p7 | 1:235731225 | TGACCATCCAGGACT[C/T]GTAGCTATAAAAAAA | 1130 |
rs765988194 | snp | A/G | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801083 | AACCTTCTGTTTCAG[A/G]CTTTAAGTCTACCCC | 1130 |
rs765989181 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702773 | TTTCTTTGACCTGTT[C/T]TCGGGTCTCCCTGAA | 1130 |
rs765997991 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819227 | AATTTCAAACACAAT[C/T]CATCATTGGGGAAGT | 1130 |
rs766003402 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235859258 | CGTTACATTTGATCA[A/G]TTATCTTCTACCTCT | 1130 |
rs766005164 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235844619 | TACTACCTCTAAATG[G/T]TATCCAGAACCTTTA | 1130 |
rs766014104 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235723897 | ATAACAAAGGCTTCA[C/T]TTTAATCAGGACTAA | 1130 |
rs766019990 | snp | C/T | 1.65392e-05 | 0.00287564 | intron-variant | LYST | GRCh38.p7 | 1:235746319 | TGAGGAAAAACAAAC[C/T]AATCCTATAGTCTTA | 1130 |
rs766035434 | snp | C/T | 1.65091e-05 | 0.00287303 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720886 | TTTGTGAGTATATTG[C/T]GGTATACATCATCAC | 1130 |
rs766043149 | snp | A/C | 1.65012e-05 | 0.00287234 | missense | LYST | GRCh38.p7 | 1:235709195 | GCGACACGTAGTCAG[A/C]CTCTAGAGCCTGCCG | 1130 |
rs766063224 | snp | A/T | 1.81922e-05 | 0.00301592 | intron-variant | LYST | GRCh38.p7 | 1:235788665 | AAATTATTTAAATAC[A/T]TTATCTATTCATGGG | 1130 |
rs766069187 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235804292 | GGAAAAGCTTATCAT[A/G]TCACTCTCCTGTTAT | 1130 |
rs766070741 | snp | A/T | 3.31268e-05 | 0.00406968 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759008 | TTGTAATTTGGCTCA[A/T]AACCAAGAGAATAGG | 1130 |
rs766081270 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235686730 | AAACAGATCTAACTC[-/A]AAATACCGTCTCTGA | 1130 |
rs766083348 | in-del | -/TT | | | intron-variant | LYST | GRCh38.p7 | 1:235856980 | GATGAAATCTCACTC[-/TT]GTCGCCCAGGCTGGA | 1130 |
rs766092229 | snp | C/G/T | 3.29599e-05 | 0.00405944 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759357 | CAGACTCACAGCTAC[C/G/T]GATGAATGCGTCCTC | 1130 |
rs766097167 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235858202 | AGTGCTTCAATGCTA[G/T]AAGGACTCAGAAAGA | 1130 |
rs766110570 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235871149 | TATTGAAGAGGTCAA[C/T]TCATAATTAATGTCT | 1130 |
rs766112457 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771083 | ATAATGAACCAAGAT[A/G]TTGATAGACTTAATC | 1130 |
rs766113671 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235747423 | TATAACAGGTTTTAA[A/C]GACTTATCCTGTAAG | 1130 |
rs766115503 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235697540 | TTGAAATTTGAGCAG[A/G]GAAAAAAATTTAGTA | 1130 |
rs766117677 | snp | A/T | 1.6507e-05 | 0.00287284 | intron-variant | LYST | GRCh38.p7 | 1:235728158 | AATTGGATATAAGGG[A/T]TTTAAAATGTATGTG | 1130 |
rs766124555 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235715513 | AGGAGACTTCAGCCT[C/T]CTTGAGTGTCTGGGA | 1130 |
rs766124885 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235733944 | TACTATATAAAATTT[A/C]TTATTTCTCACCTAA | 1130 |
rs766136904 | snp | C/T | 2.05916e-05 | 0.00320864 | intron-variant | LYST | GRCh38.p7 | 1:235812932 | CTTTTCTATGAAATT[C/T]TGATAACACAAGTGA | 1130 |
rs766147858 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235732107 | TTTAATTTGTAGTTA[G/T]GATCATTATGATCAT | 1130 |
rs766155381 | snp | G/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791789 | TACTCTCAGCTTCAT[G/T]GATACACTCCACATT | 1130 |
rs766175219 | snp | A/C/G/T | 6.61941e-05 | 0.00575271 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791877 | CAACGGCAGGTGGAC[A/C/G/T]GGGGCTATGTGCCAA | 1130 |
rs766191808 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684456 | TTTAGAATCGATTTG[A/T]AGGGGAAGTCAGAAA | 1130 |
rs766233496 | in-del | -/C | 4.97574e-05 | 0.00498761 | intron-variant | LYST | GRCh38.p7 | 1:235766074 | ACAAAAATGATTATA[-/C]CTACCTATGTGCAAA | 1130 |
rs766237620 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235757526 | GATTACCTTAGGAAC[C/T]GTGACAAGTAGTAGC | 1130 |
rs766253474 | snp | A/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826969 | ACTACTGATGTGAGG[A/T]GTATTTGTCACTATT | 1130 |
rs766265874 | in-del | -/TA | | | intron-variant | LYST | GRCh38.p7 | 1:235742572 | GTAAATTTTATGTTA[-/TA]TATATATATATATAT | 1130 |
rs766272501 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753164 | AGAAGAAGTAAAAGA[A/G]CATTATGCAAGAGTA | 1130 |
rs766279837 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685373 | CCCTTGGAAGTGTTT[C/T]TCCTTGCAGGCTCTA | 1130 |
rs766281686 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672280 | TCATTAGGGAATAAC[C/G]ATGACTTTGGATAAG | 1130 |
rs766288052 | snp | A/T | 1.66054e-05 | 0.00288139 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808849 | CAGCATCACATAAGT[A/T]TCCCTGCAGTGTCTC | 1130 |
rs766299858 | snp | A/G | 1.85872e-05 | 0.00304848 | intron-variant | LYST | GRCh38.p7 | 1:235777341 | TCATTCAGTAATGAC[A/G]ACAAGTTTAAAATGC | 1130 |
rs766304531 | snp | C/G | 1.65891e-05 | 0.00287998 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810022 | ACTTACAAACTTTTT[C/G]TAATAAAGATAACAA | 1130 |
rs766310541 | snp | A/C | 3.42384e-05 | 0.00413739 | intron-variant | LYST | GRCh38.p7 | 1:235709350 | TTAACTCCCCCACAG[A/C]AAGTTTCATTCAGCT | 1130 |
rs766324119 | snp | C/G | 1.64991e-05 | 0.00287215 | missense | LYST | GRCh38.p7 | 1:235677597 | TAGAGATGTATTTGA[C/G]TCTCCATTTCTATTT | 1130 |
rs766390727 | snp | A/G | 2.46856e-05 | 0.00351314 | intron-variant | LYST | GRCh38.p7 | 1:235746543 | CTTTAAAAGTATATA[A/G]ATTAAAACATCAAAT | 1130 |
rs766397951 | snp | C/G | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868619 | GGTATACAATTGGCC[C/G]TCAAAGTATTATTTG | 1130 |
rs766399799 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882624 | AAGGTGTTAAGAGTG[G/T]GTAGGAACCTACAAG | 1130 |
rs766407725 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235694816 | AGGTTTCTCATTCCA[A/G]TACCACAAGAGGCAT | 1130 |
rs766412027 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235718614 | ACTCTTTGGCACTTA[A/C]AGCTGAAATACTCTA | 1130 |
rs766416099 | snp | C/T | 1.65007e-05 | 0.00287229 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751197 | GTTATTAAAATATGA[C/T]TTCAATACTCGCCAG | 1130 |
rs766432974 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235859840 | GATGTTGTCAGGGTT[A/C]AATAAAATAATAAAT | 1130 |
rs766441936 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800878 | TTTTTTACCTGTTGC[A/G]TGAGCAGAAAAACAT | 1130 |
rs766464279 | snp | A/T | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773963 | TTCATATAAATAATA[A/T]CTTCACCACAGCATC | 1130 |
rs766466824 | snp | A/T | 1.66117e-05 | 0.00288194 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744131 | TTTCTGGAGTTCTCA[A/T]AATGTCAATAATGTC | 1130 |
rs766468813 | snp | A/C | 9.91834e-05 | 0.00704144 | intron-variant | LYST | GRCh38.p7 | 1:235755437 | AGAAAAGAAAAAAGA[A/C]AAAAGATTCCCAATT | 1130 |
rs766481487 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685297 | TAACCTGCCCTTCTT[C/T]GCTTCCTGCCTGGAT | 1130 |
rs766486214 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235749554 | CCCAGTTCTAGGATG[C/T]AGTGGGTCTTAAGAT | 1130 |
rs766489249 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862186 | TGACTGACATAAGGA[A/T]GTCCCATCTGCTTTA | 1130 |
rs766507211 | snp | A/G | 8.51346e-05 | 0.00652381 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235782057 | ACTTGTTTTTCTTGG[A/G]AGCATAAAATCCAAA | 1130 |
rs766509659 | snp | C/T | 4.94727e-05 | 0.00497332 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830327 | CCTCCTCTTCTTCCT[C/T]CCTGGCCTCCACCCT | 1130 |
rs766554765 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235820578 | GTTTTGCCATGTTGC[C/T]TAGGCTGGCCTTGAA | 1130 |
rs766558534 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | LYST | GRCh38.p7 | 1:235728055 | AGATTTATGTAAATA[C/T]AGACTTAAGCCTCTA | 1130 |
rs766575718 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759222 | CATCTTCTGACCTGG[A/G]TTCTGCTCCCAACTG | 1130 |
rs766582872 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743297 | GCTCCTCTCTAATTA[C/T]ATCTAGTCCTAAGGG | 1130 |
rs766596704 | snp | C/T | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757343 | CCAAAAGTGTATCTG[C/T]TTGAATAAGCTTGTC | 1130 |
rs766612193 | in-del | -/CTCTTGGAA | | | intron-variant | LYST | GRCh38.p7 | 1:235710806 | CCTCTGTTCGTCTCC[-/CTCTTGGAA]CACTTGTCTTTGGAA | 1130 |
rs766627609 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738510 | GACTCAGCCCAATTC[C/T]GTTACCCAATGGGGG | 1130 |
rs766650024 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806615 | GTTCAATGTCTATCC[C/G]ATCAATATCTGGAAC | 1130 |
rs766666036 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235835426 | CAGCGTGGCCGTAAG[A/C]AGTGAAAGCTGGCAG | 1130 |
rs766670822 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727936 | ATATTTAAAAAAATG[G/T]TTGGAACTCAGACCA | 1130 |
rs766672894 | snp | C/T | 3.39605e-05 | 0.00412057 | intron-variant | LYST | GRCh38.p7 | 1:235743952 | CTTTGTGTGAATGAA[C/T]ATTTCCCATGTAATT | 1130 |
rs766689159 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672041 | ATAGCTTGGATATAA[A/G]GAGAAAGAAGGAGAA | 1130 |
rs766689192 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235699738 | CAGCCTCACCAGCAT[C/T]CATTGTTCCTTGACT | 1130 |
rs766712442 | snp | A/T | 6.59826e-05 | 0.00574343 | intron-variant | LYST | GRCh38.p7 | 1:235731014 | TATTTATATGTTGAG[A/T]CAAGAAGCCACTATT | 1130 |
rs766713231 | in-del | -/AA | 1.66333e-05 | 0.00288381 | intron-variant | LYST | GRCh38.p7 | 1:235702988 | TATGTCTGCAGAGTG[-/AA]AGAGTAAAGGAACAA | 1130 |
rs766715045 | in-del | -/CTAC | | | intron-variant | LYST | GRCh38.p7 | 1:235844605 | CCCTAACACTAAATA[-/CTAC]CTACCTCTAAATGGT | 1130 |
rs766721219 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon | LYST | GRCh38.p7 | 1:235662973 | GCTAAGGAAGGAATA[A/G]AACATTGGCTGTTTC | 1130 |
rs766739250 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785613 | GCAACATAGTAAGTA[C/T]GCAGTATTATATTCC | 1130 |
rs766760874 | snp | G/T | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741556 | GTCTCCCAAGCTGCA[G/T]TCGGAAGGTCTCCTT | 1130 |
rs766769810 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235681023 | GAACCAGGAGCTGGG[A/G]ATACAGAGTTCCCCT | 1130 |
rs766782240 | snp | A/G | 1.79252e-05 | 0.0029937 | intron-variant | LYST | GRCh38.p7 | 1:235775134 | CCCAATTTGCTGAGA[A/G]TAAAAATTTAACATG | 1130 |
rs766785648 | snp | A/G | 3.29919e-05 | 0.00406138 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809127 | GTGCTGCTCAAGGAA[A/G]CCTGCTGTAGTAAGC | 1130 |
rs766786476 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873820 | CAATAGACAGGCTAA[A/G]AAGTACAAGGAAATT | 1130 |
rs766789616 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235726214 | ACTCAATTGCCAAGA[A/G]CTATTTTATCCTAGG | 1130 |
rs766799151 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235842481 | AACAGATCATTGTAA[A/G]TTCTTAAAATGAAAG | 1130 |
rs766804617 | snp | A/G | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805881 | TAGCTTTGCTTCCTC[A/G]GGAGCGGCTTCAGTA | 1130 |
rs766815117 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805974 | AGCACTCTTTTTTAG[A/G]CTACCTAGTTCTGAT | 1130 |
rs766823455 | snp | A/G | 3.31713e-05 | 0.00407242 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809850 | AAGAGCATCCTTTGA[A/G]TCAAAGCCACCGGTT | 1130 |
rs766847907 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235756700 | ACACAAGATGCCCAC[C/G]CTCATGGAGCTTATA | 1130 |
rs766858122 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235700084 | CCTTATACAAAAATT[A/C]ACTCAAGATGAATTA | 1130 |
rs766859899 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669784 | TTCAATAAATTCCTG[C/G]TTTTGTTCTTTTGTT | 1130 |
rs766862486 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731142 | GGATCCAACTGCCAT[A/G]AGGTTGGATAGTAGA | 1130 |
rs766869010 | in-del | -/A | 0.0451752 | 0.143342 | intron-variant | LYST | GRCh38.p7 | 1:235830442 | TAAAATAAGTATTAC[-/A]AAAAAAAAAAGATTA | 1130 |
rs766882273 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235699394 | CTTCCAGCTTCATCC[A/G]TGTCCCTGCAAATGA | 1130 |
rs766885431 | in-del | -/CGG | 4.95176e-05 | 0.00497558 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806389 | TGGCCGACTCCCTGT[-/CGG]CAGACTCTGCTTCTT | 1130 |
rs766888040 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235856402 | CTCTTTAGGATCTCA[A/G]GCAAGGTGCTTAACC | 1130 |
rs766890134 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841213 | GTTTCCAATACCAGA[C/T]CGAATAAGGAAATAG | 1130 |
rs766895470 | snp | C/G | 2.06315e-05 | 0.00321175 | intron-variant | LYST | GRCh38.p7 | 1:235792143 | AGAGAAAAAGAAAAA[C/G]AAATGAAACTTTCTA | 1130 |
rs766910518 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235749919 | AGGACTATTGTGTTA[G/T]CCCAGGCACAAGGTG | 1130 |
rs766917496 | snp | A/C | 1.65515e-05 | 0.00287671 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788805 | TTCTATGAGTCTTTC[A/C]CCAGGATTTATGTAC | 1130 |
rs766939862 | snp | A/C | 6.59914e-05 | 0.00574381 | missense, intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235770220 | TTTCAATAACTGCTT[A/C]ATATTAAACATCTGC | 1130 |
rs766950203 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235695323 | CCCAAGGCCACATAG[C/G]TAGTAAGCAGCAGGG | 1130 |
rs766974997 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235720410 | TATTTTTTAAAGAGA[C/T]GCATACTGTAGAACA | 1130 |
rs766989559 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235795671 | AGCTCTTCCACATAC[C/T]ACCCACTCAGGAAAG | 1130 |
rs767011816 | snp | C/T | 1.94471e-05 | 0.0031182 | intron-variant | LYST | GRCh38.p7 | 1:235751966 | CAGGTTTGTCTGTTA[C/T]ACAACTCCCTCCCCA | 1130 |
rs767041109 | snp | C/T | 1.6638e-05 | 0.00288422 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762829 | CATGATTGACCGCAC[C/T]TTCTCCTGAAAGATC | 1130 |
rs767043095 | snp | A/C | 2.07183e-05 | 0.0032185 | intron-variant | LYST | GRCh38.p7 | 1:235755692 | AATGCATTAAAATTA[A/C]ATATAATATATACAA | 1130 |
rs767058015 | snp | A/C | 1.65564e-05 | 0.00287714 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759018 | GCTCATAACCAAGAG[A/C]ATAGGCAAAGTTTTC | 1130 |
rs767062870 | snp | A/G | 3.31494e-05 | 0.00407107 | synonymous-codon | LYST | GRCh38.p7 | 1:235664575 | GTGGACATGTCCAAC[A/G]AGATCCCCGTTCACC | 1130 |
rs767077644 | snp | C/T | 1.65811e-05 | 0.00287929 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801097 | GACTTTAAGTCTACC[C/T]CTGAAAAGAGAAAAG | 1130 |
rs767079188 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702872 | TGCTCACATGGGCCA[C/T]GTGGAACAGCTGACG | 1130 |
rs767084043 | snp | C/T | 1.65206e-05 | 0.00287403 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809464 | AAACCAGCCATTCCA[C/T]TTGAAGAACTGCTGT | 1130 |
rs767088366 | snp | A/G | 1.65833e-05 | 0.00287948 | intron-variant | LYST | GRCh38.p7 | 1:235720911 | CATCACGAACCTAAA[A/G]GGGAAGGAGAAGAAA | 1130 |
rs767091110 | in-del | -/AAA | 1.65802e-05 | 0.0028792 | intron-variant | LYST | GRCh38.p7 | 1:235755429 | AAAAGAAAAGAAAAG[-/AAA]AAAGACAAAAGATTC | 1130 |
rs767094821 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738480 | AACCATGTTATTGGA[A/C]GTGGTTGCAATCTGG | 1130 |
rs767141432 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674044 | AAGACCCCACAGCCC[A/G]GGGCAATAAGGCATG | 1130 |
rs767152361 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746338 | CCTATAGTCTTACCT[C/T]GATAAATAATCCTGT | 1130 |
rs767152978 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705783 | TTAATGTTAAGATTC[C/T]TAATTGCTCTTTTTA | 1130 |
rs767158670 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235845895 | CACCTGATGGTCCTT[C/T]CCTATCCACCCTGGT | 1130 |
rs767166436 | in-del | -/A | 6.78979e-05 | 0.00582618 | intron-variant | LYST | GRCh38.p7 | 1:235766280 | CTCTTTGTATTCCTG[-/A]AAAAAATAAAAAAAA | 1130 |
rs767170253 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235879395 | GCAGGGAGCATATGG[A/C]GGGAATGGTCGCCTG | 1130 |
rs767186673 | snp | C/G | 1.66208e-05 | 0.00288273 | intron-variant | LYST | GRCh38.p7 | 1:235702983 | CAAAATATGTCTGCA[C/G]AGTGAAAGAGTAAAG | 1130 |
rs767215319 | snp | C/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762548 | AATGCCAGAACAAGA[C/T]AGCATGAGCCTCATC | 1130 |
rs767218260 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235728321 | GCTTTACCTCTTTGT[A/G]TCTTAATTTCTTTAT | 1130 |
rs767227173 | in-del | -/TAC | | | intron-variant | LYST | GRCh38.p7 | 1:235833167 | TTTGTATATTAGGAA[-/TAC]GTATTCACCTCTTCC | 1130 |
rs767229494 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235674835 | GCAAATAAATTAGCC[A/G]AAAAGTCATAGAAAA | 1130 |
rs767238172 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235663823 | AGGAGTGTGGTCTCT[C/G]TTGCTGCTGGGTCAC | 1130 |
rs767240387 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant | LYST | GRCh38.p7 | 1:235755452 | CAAAAGATTCCCAAT[C/T]ATAGTGGAGGGAAGA | 1130 |
rs767241699 | snp | C/T | 0.000116437 | 0.00762921 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775014 | GTACTCTTTGTTGGT[C/T]GTATTTAATTAATGA | 1130 |
rs767243198 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706962 | CTACTGTAGGTTCTG[G/T]GTGTGCACTTTACCT | 1130 |
rs767244777 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235859381 | CCCAATGATCACATC[C/T]ACTTCCTCAAGCTTC | 1130 |
rs767284526 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235724038 | TTTACCTTGGTGTTA[C/T]CAAATGCCAACAGGA | 1130 |
rs767284805 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235860453 | GCTACCACTGTAGTA[A/T]CTTCAGAATAGTTTC | 1130 |
rs767288291 | in-del | -/ATTTT | | | intron-variant | LYST | GRCh38.p7 | 1:235856940 | ACACAGGATATACTG[-/ATTTT]TTTTTTTTTTTTTTT | 1130 |
rs767289429 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235788994 | TGTTCTAAACAACCA[G/T]ATTTTCAGAGTATAG | 1130 |
rs767305219 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235744953 | GCTAAAAAAATAATA[A/G]TAACTTGAGTTTATC | 1130 |
rs767308343 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838120 | CAATAGGAGGACCAA[G/T]AATTTTTTTCAGGTG | 1130 |
rs767345210 | snp | C/T | 3.32132e-05 | 0.00407499 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808866 | CCCTGCAGTGTCTCT[C/T]CTAATTGGGCTAGTT | 1130 |
rs767372373 | in-del | -/A/AA | 0.0672227 | 0.170582 | intron-variant | LYST | GRCh38.p7 | 1:235663082 | AAAATGTAAGGCTGT[-/A/AA]AAAAAAAAAAAAATT | 1130 |
rs767380219 | snp | C/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806292 | AGAAGGCAAGACAAG[C/G]CTCTCGAGAGATATA | 1130 |
rs767386693 | snp | G/T | 1.72967e-05 | 0.00294076 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780935 | TCACATCGCAAAATT[G/T]CTTTATTAATATATT | 1130 |
rs767396352 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235848555 | GAAATTGAAACAAAC[-/A]AAAAAAAATACAAAA | 1130 |
rs767422000 | snp | C/G | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738842 | GATTGGTGGAATAAA[C/G]GATGATGTCTTCCTT | 1130 |
rs767422639 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235670959 | ATATGATTCCCTCTG[A/T]TAACCCTCTAAGTCT | 1130 |
rs767424814 | snp | C/G | | | synonymous-codon | LYST | GRCh38.p7 | 1:235697183 | AAATCTTTCTCCGTG[C/G]GGCTGGCTGAAGCAG | 1130 |
rs767438292 | snp | A/G | 1.77827e-05 | 0.00298178 | intron-variant | LYST | GRCh38.p7 | 1:235766322 | TTTAAAGAATTGTCA[A/G]CTTAACTAAGATTTT | 1130 |
rs767440335 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817573 | TTTGTAGCAATATGG[A/T]TGGACGCTGAGGTCA | 1130 |
rs767447517 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | LYST | GRCh38.p7 | 1:235687020 | TAAACAGCTGGCAAC[G/T]GTCAGGCACCCAAGC | 1130 |
rs767448803 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235663490 | CTAAAAGAGAAAAGG[-/A]AAAAAAATGTAACAT | 1130 |
rs767473828 | snp | C/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806204 | TATAAAACTGTTTCT[C/G]GAACACTGAACTCAA | 1130 |
rs767475445 | snp | C/T | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235865483 | CTGACACGCAGTAGG[C/T]GCTCAATAAATATTT | 1130 |
rs767480763 | snp | C/T | 1.95006e-05 | 0.00312249 | intron-variant | LYST | GRCh38.p7 | 1:235777356 | AACAAGTTTAAAATG[C/T]AAGCTATGAACTAGC | 1130 |
rs767482498 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791967 | TCGTGCTCTTCTCAA[C/T]AAACCCATGGCCTTA | 1130 |
rs767491007 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805913 | CTGAAACTTCTTCCA[C/T]ATTTATGGAAGAAAT | 1130 |
rs767509696 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235790949 | GAGAAAGAAGTTTGC[A/G]ACCAGCCTGACCAAC | 1130 |
rs767527570 | snp | A/T | 1.90228e-05 | 0.003084 | intron-variant | LYST | GRCh38.p7 | 1:235812955 | ACAAGTGATATGATA[A/T]AGGGAAAAAGCATAC | 1130 |
rs767552471 | snp | C/T | 3.30224e-05 | 0.00406326 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746439 | TTGGCTCATTCTCCG[C/T]TGCATCATCACATGA | 1130 |
rs767558843 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235684282 | GTGCACAATTAAAAA[C/T]GGAGAAGTAGGGAAA | 1130 |
rs767565425 | snp | C/T | 2.27637e-05 | 0.00337363 | intron-variant | LYST | GRCh38.p7 | 1:235804716 | ACCATTTTAAAAAAC[C/T]AAATGATGAAAAAAT | 1130 |
rs767571020 | snp | C/T | 4.95299e-05 | 0.00497619 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830344 | CTGGCCTCCACCCTC[C/T]GGACCACTGCATTGC | 1130 |
rs767573807 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813411 | CCCTATTAATTAGCA[A/G]AGCAATGCTACAAAG | 1130 |
rs767579224 | snp | C/T | 1.76789e-05 | 0.00297307 | intron-variant | LYST | GRCh38.p7 | 1:235734675 | CTTTAAAAAAAGTAA[C/T]AATTTTTTAGTCATT | 1130 |
rs767580093 | snp | C/G | 1.95586e-05 | 0.00312712 | intron-variant | LYST | GRCh38.p7 | 1:235774884 | TCACTGCATATGAAA[C/G]TATAAGAATAAATTT | 1130 |
rs767596629 | snp | C/T | 1.65386e-05 | 0.00287559 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773969 | TAAATAATATCTTCA[C/T]CACAGCATCCTTCAA | 1130 |
rs767614294 | snp | G/T | 6.62548e-05 | 0.00575526 | intron-variant | LYST | GRCh38.p7 | 1:235730796 | ACATAAACACTACAA[G/T]AAGCTGTTGTATATT | 1130 |
rs767628297 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235812350 | CTGTATGTACTAAAA[C/T]GCAAAAATTAGTCTG | 1130 |
rs767634885 | in-del | -/AAAC | | | intron-variant | LYST | GRCh38.p7 | 1:235850582 | AACAGTCAGCAGAGT[-/AAAC]AAACAACCCACAGAA | 1130 |
rs767638134 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235715594 | ATCTCCACCTTCACT[A/C]TTTCATTCCCTCATA | 1130 |
rs767650679 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672114 | ATTCTGAAATTCAGA[A/G]ATGAGGCATACCAGA | 1130 |
rs767666760 | snp | A/T | 1.64803e-05 | 0.00287052 | intron-variant | LYST | GRCh38.p7 | 1:235663946 | AAAATACAATCACAA[A/T]TTGTATTCTGAAGCA | 1130 |
rs767687843 | snp | G/T | 0.000148303 | 0.00860985 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787357 | CTTTCATGTCATCAT[G/T]TGAATCCATGCACAC | 1130 |
rs767702515 | in-del | -/ACAGT | | | intron-variant | LYST | GRCh38.p7 | 1:235713475 | CCTACATTTTATTAA[-/ACAGT]ACTACTACAAATTCC | 1130 |
rs767705019 | snp | A/C | 5.36553e-05 | 0.00517926 | intron-variant | LYST | GRCh38.p7 | 1:235712043 | TATAAATTAAAAATA[A/C]TTTATTGCTATACCT | 1130 |
rs767713124 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235850898 | TGGCATGGACGTGGT[C/G]AACAGGGAACACTTC | 1130 |
rs767720854 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235878930 | AAGTGCAATTGTATT[-/A]CATGGATATATTGAG | 1130 |
rs767723673 | snp | A/C | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884743 | TGGATTTCTGAATTA[A/C]TATTTTTATTTAGAA | 1130 |
rs767727894 | in-del | -/ATCT | | | intron-variant | LYST | GRCh38.p7 | 1:235726497 | CTCTGCATGAAATAC[-/ATCT]GTATGGGTCAAAAAG | 1130 |
rs767733533 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235758558 | TGGAGCCGTCACTTG[C/T]CTCTGATCAAGTAAG | 1130 |
rs767740055 | snp | A/G/T | 8.24023e-05 | 0.00641838 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751301 | AGAGTCATGATTTGC[A/G/T]GTGGTCCTTATAAAT | 1130 |
rs767740744 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862921 | AACACTTGTTCTATT[G/T]TATAAAATGAGGTGT | 1130 |
rs767768095 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710946 | AAGAGAGGGTGATGT[C/G]CTCCAGCTGCCTAAG | 1130 |
rs767774418 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759440 | TGGGTGGCAACATAA[A/G]TATCTGCAATATTTT | 1130 |
rs767785336 | snp | A/C | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791884 | AGGTGGACTGGGGCT[A/C]TGTGCCAAGATGAAA | 1130 |
rs767791732 | snp | C/G/T | 6.64246e-05 | 0.00576268 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809912 | CTCCAAGTTGTCGCT[C/G/T]AGACTGCAGCAGTCC | 1130 |
rs767798238 | snp | C/T | 4.94474e-05 | 0.00497205 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804562 | TTCCCGAGGGCAACT[C/T]GAAGCAGGGCATCAA | 1130 |
rs767801254 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235863584 | TGAAATTCCAGACTA[C/T]ATGGCTCTCTCTACA | 1130 |
rs767809475 | snp | A/C | 1.65031e-05 | 0.00287251 | intron-variant | LYST | GRCh38.p7 | 1:235731197 | AAGTAAAAAGATTAA[A/C]GGGTGTTTTAAGTGA | 1130 |
rs767819421 | snp | A/G | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810379 | GATGGGTAATTTTAC[A/G]CTGTCGTCTGCTTTT | 1130 |
rs767823423 | snp | A/G | | | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741624 | CCACTGGCTTTACTT[A/G]AACCCTAAAATCAAT | 1130 |
rs767865573 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant | LYST | GRCh38.p7 | 1:235664061 | GCTCCATAACCTAGA[A/G]GGGAAAAAAATCATC | 1130 |
rs767868632 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787213 | ACCTCTGTCCAGAGA[C/T]CCATATGGAGATTTT | 1130 |
rs767877661 | snp | A/G | 8.29772e-05 | 0.00644063 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830390 | CGGTCAGAAATTCAC[A/G]TGCCAGTGAGTTACT | 1130 |
rs767888264 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235672990 | CACCGACACCAACCC[A/G]GAGATCACATCCTTA | 1130 |
rs767889083 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon | LYST | GRCh38.p7 | 1:235697210 | GCAGACCACAGGTAC[C/T]GGAGCACTGGGGGAA | 1130 |
rs767893165 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806512 | TCTTTGAGGCCAGCA[C/T]AAAATTTGCTGAGAC | 1130 |
rs767895198 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235700121 | AATGTAAAACCCAAA[A/C]CCATAAAAACCTTAG | 1130 |
rs767901794 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235778492 | CAATTCTCCTGCTTC[A/G]GCCTCCTGAGTAGCT | 1130 |
rs767934874 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235880043 | TGCCCAGACTGAGAA[G/T]GGATCTAAGTTTCTC | 1130 |
rs767954844 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808341 | AGCCCTGGAGATATC[A/G]GTGTTAGAAGTTTAA | 1130 |
rs767960827 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235667578 | ATTGGTTCCAGGACC[C/T]CTGAGGATATCAAAA | 1130 |
rs767964898 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235678597 | AGAAAAGTAGAAAGA[A/G]TAAGTATAATAAAGA | 1130 |
rs767977915 | snp | G/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235757385 | CAAGCAAAACATCAG[G/T]CAGGATAAGAAGAAC | 1130 |
rs767981771 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852980 | TCAGAGCATTTTAGC[A/G]ATTAGGTCTGGCACA | 1130 |
rs767996620 | snp | A/C/G | 3.30635e-05 | 0.00406581 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793579 | CTTGAACTCATCAAA[A/C/G]ATACCAAAAGATCCA | 1130 |
rs767997947 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809288 | ATCTCGGTGATGATG[C/T]ATAAAATGAGAATAT | 1130 |
rs768014376 | snp | C/T | 1.65811e-05 | 0.00287929 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810470 | TTTTTCCTGAGTGGA[C/T]CTTTGTGAACTTGAG | 1130 |
rs768016222 | snp | C/T | 1.64974e-05 | 0.00287201 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809190 | CAGCACCGCTCAGGA[C/T]AATAAACATCTCCAT | 1130 |
rs768031735 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235773815 | TTTACCACAATAAAA[A/T]ATGGAAAAAAAGTAC | 1130 |
rs768039260 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235843961 | GTATTAGAGAAGTTG[A/C]CATTGGAAAGACTTT | 1130 |
rs768044934 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807258 | AGAGCTGAAAATCTA[C/T]GGAAGGCTCAGCATC | 1130 |
rs768049018 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235821486 | TTCTAATCTTTGTAT[A/G]TGAAAGAAATCCTCT | 1130 |
rs768059517 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235784026 | CTGGGACTACAGCTA[C/T]GCATTACCATGCCCA | 1130 |
rs768065591 | snp | A/G | 3.30327e-05 | 0.0040639 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806089 | TTTTCATTTACACTT[A/G]TATCTCCCTCCTTTT | 1130 |
rs768082763 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235747756 | TAATACTAGAAAACG[C/T]GGGAGGGTATTTCAG | 1130 |
rs768105154 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235876405 | CACTTTGAGTTTACT[-/A]AGTTGTGGGAACTGC | 1130 |
rs768123871 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235823910 | CCTGGTAAAGACAGT[C/T]GCTGTCCTTTCATCT | 1130 |
rs768135003 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235731344 | TACAAGTAGAAGTAA[C/T]AAAATCTAAGTGTCT | 1130 |
rs768142892 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669649 | CTTCATTCACATGAC[A/G]TGAGCATAAAGTGGC | 1130 |
rs768143916 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235728806 | TGTGACGGTGGGGCT[C/G]AGTCCCAGCAGGCTT | 1130 |
rs768154100 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870860 | ATAAATATCCAAACA[A/G]TAAGTTGACCATAAT | 1130 |
rs768159314 | in-del | -/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884792 | ATAAACAATGGCATT[-/T]TTTTTTTTTTTTTCA | 1130 |
rs768164137 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734613 | GTCAATTCACCTTGG[C/T]GATTATGTATCAACT | 1130 |
rs768173306 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235714535 | AAGAATGGTTGAGTA[A/G]AAGAATGGATAATGA | 1130 |
rs768176110 | snp | G/T | 1.65795e-05 | 0.00287914 | intron-variant | LYST | GRCh38.p7 | 1:235757480 | CAGAGACCAAAAAAG[G/T]CTTACTAACATGACA | 1130 |
rs768178180 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235729021 | TGCTGATGCTACTAA[C/T]TCAGGGTTCTCACAC | 1130 |
rs768183856 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883374 | TTATTCCCCTGGCAT[C/T]GAGGAACACACACGG | 1130 |
rs768190475 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, downstream-variant-500B, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751216 | AATACTCGCCAGCAA[C/T]GCTTTTCCGCTTTTG | 1130 |
rs768191566 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235754545 | TGTCTTTTCAGTTAA[A/T]CTTCTCATGTTAATA | 1130 |
rs768195022 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822615 | TTCAAGAGGCGTAGA[A/G]GGGAGTGAGTGTAGG | 1130 |
rs768197548 | snp | C/T | 6.6084e-05 | 0.00574784 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830365 | ACTGCATTGCAAAGC[C/T]GGTTGACATCGGTCA | 1130 |
rs768206502 | snp | A/T | 1.67705e-05 | 0.00289568 | intron-variant | LYST | GRCh38.p7 | 1:235663090 | AAGGCTGTAAAAAAA[A/T]AAAAATTCCCATTTG | 1130 |
rs768216263 | snp | C/G | 1.67105e-05 | 0.0028905 | intron-variant | LYST | GRCh38.p7 | 1:235803088 | CAGTGTAATTCAAAG[C/G]TTGTAACATTTGCTT | 1130 |
rs768230702 | snp | G/T | | | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809455 | CATCTCTTAAAACCA[G/T]CCATTCCATTTGAAG | 1130 |
rs768237345 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235787677 | TTTATATAGCCATTG[A/C]CCATTTAGAAATTAC | 1130 |
rs768246124 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713055 | CTGCCACAAACACAT[C/T]GCAGCATCAGGTTTC | 1130 |
rs768247031 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791862 | GCAGTTTTGCCCCAG[C/G]AACGGCAGGTGGACT | 1130 |
rs768254200 | in-del | -/TTTTA | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235868694 | TTCGGTACCAGTGTT[-/TTTTA]TTTTATTTTATTTTC | 1130 |
rs768259074 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235835957 | CAACAATTGTTATAA[C/T]GTCATAACAAAGAAA | 1130 |
rs768264683 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235751570 | AAAAAACCTTCAATG[C/G]AAAAATATTAGCTCA | 1130 |
rs768270867 | snp | A/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806571 | ATGATGAAAAGAAGT[A/T]CCCACATGTACAGAG | 1130 |
rs768272074 | snp | A/C | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759329 | ACAGCTTCCATTTCA[A/C]AAACAGTTTTTGCAG | 1130 |
rs768279992 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235727828 | ATGAACATAAATTGA[C/T]ATAATAGGAGCATTT | 1130 |
rs768310949 | snp | A/C | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773929 | AGAGTCTACATCCAA[A/C]TTAAACTCTCCATTC | 1130 |
rs768314799 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235811296 | AAATCTCTTCCCATA[A/G]TACCACTAATTAAAA | 1130 |
rs768326732 | snp | A/G | 3.29582e-05 | 0.00405931 | intron-variant | LYST | GRCh38.p7 | 1:235663973 | AGCATAAGAGGGGGA[A/G]AAGATCTTACCTGAT | 1130 |
rs768333423 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235851919 | TTCACAAACTGAAAT[C/T]TTCCATAAGACAAAT | 1130 |
rs768333640 | in-del | -/GAGGAGAGTTCA | 1.66109e-05 | 0.00288187 | cds-indel, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808824 | GGACTGGATAAACTT[-/GAGGAGAGTTCA]GCATCACATAAGTTT | 1130 |
rs768356369 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728116 | TTATCTTCCACAAAA[C/T]ACATTCCACATTTAC | 1130 |
rs768387318 | snp | A/G | 1.65935e-05 | 0.00288036 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809871 | GCCACCGGTTCTTCG[A/G]TCCAACCTGCAGAAA | 1130 |
rs768399491 | snp | A/G | 4.97492e-05 | 0.0049872 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753115 | ATTATCCAGCAACAT[A/G]TCTGCTACCTTAGAA | 1130 |
rs768404620 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826929 | CTCAAGTAATCCATC[C/T]ACCTCGGCCTCCCAA | 1130 |
rs768406406 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235796614 | GGATCTTTGGGAGGT[G/T]ACTGGGTCATGAGGA | 1130 |
rs768407081 | snp | A/C/T | 0.000102681 | 0.00716456 | missense | LYST | GRCh38.p7 | 1:235709275 | TTGACGTGATTAACC[A/C/T]GTTCACCATTCTGAC | 1130 |
rs768415254 | in-del | -/GG | 1.65274e-05 | 0.00287462 | intron-variant | LYST | GRCh38.p7 | 1:235804692 | AAAAGAGACTAAGAA[-/GG]TATTAATAACCATTT | 1130 |
rs768438184 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756068 | ATCTATATCTGTATC[C/T]ATATCTATCCTAGAC | 1130 |
rs768446710 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676145 | ACAAAACACTCTTGA[C/T]TAGGTGATATATTTT | 1130 |
rs768450068 | snp | A/G | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662316 | TTCTGGTTCTCCTTT[A/G]AGCTAAGAAAGCAAC | 1130 |
rs768454456 | snp | A/C/G/T | 6.88156e-05 | 0.00586551 | intron-variant | LYST | GRCh38.p7 | 1:235715405 | ATTGTGGGCTCCAGG[A/C/G/T]AACGCTAGAAAAGTG | 1130 |
rs768465067 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235856009 | CCATGTGTGAAGATG[G/T]ATAGTTAGGGGAGCA | 1130 |
rs768474206 | snp | A/T | 6.68807e-05 | 0.00578238 | intron-variant | LYST | GRCh38.p7 | 1:235755659 | ATAGCTAAACAAAAA[A/T]TTTAAGTCAATTTAG | 1130 |
rs768487753 | snp | C/T | 1.65332e-05 | 0.00287512 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716724 | TACCTTGTATGTGTC[C/T]ACATAACGATCTTCT | 1130 |
rs768493053 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235700854 | AAGACAGACAAAGTC[C/G]TTGTGTTTATGGAGT | 1130 |
rs768493075 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687610 | GCACCACTCAGGTTT[C/G]AGTCAATTTTCTATG | 1130 |
rs768505749 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235818940 | TCAGACCCAGCAACA[A/C]CTCTTCTGTGGAGCT | 1130 |
rs768509594 | snp | G/T | 1.67733e-05 | 0.00289592 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235793505 | ATAGCATATTTACTG[G/T]ACAAGGAGATTTCTC | 1130 |
rs768522588 | snp | A/G | 4.94711e-05 | 0.00497324 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810101 | CAAGGCAGCTGGCTC[A/G]CTTAAAATGTCAGTG | 1130 |
rs768522827 | snp | C/T | 3.30475e-05 | 0.00406481 | intron-variant | LYST | GRCh38.p7 | 1:235787157 | TAATGAAACATAACA[C/T]TGTAACTGAGATTGA | 1130 |
rs768529242 | snp | C/T | 1.64846e-05 | 0.0028709 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731168 | GTAGATGGGGTCATA[C/T]CATACTGCTCTGCAA | 1130 |
rs768532041 | snp | A/G | 1.6601e-05 | 0.00288101 | missense, utr-variant-3-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762815 | GAATGCCTCAGGTAC[A/G]TGATTGACCGCACTT | 1130 |
rs768545168 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235879103 | CTCAAACCCCTGGGC[G/T]CAAGCAATCCTCCCA | 1130 |
rs768548271 | snp | G/T | 1.64814e-05 | 0.00287061 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751249 | CTACTGCATGATGGG[G/T]AGCAGAAGGTGACTG | 1130 |
rs768548348 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706557 | TTGCATTAAATAAAT[G/T]TATATGCTTTTCTCT | 1130 |
rs768556726 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235780083 | GCAATACTTTGAAAG[C/T]AAAATTCCTAATTTT | 1130 |
rs768559373 | snp | G/T | 1.68937e-05 | 0.0029063 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752156 | AGCAAGCAATTTATA[G/T]TCACTCATGGGAATG | 1130 |
rs768561960 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235831370 | CGTATAGTGTGGGTT[A/G]CAAAGAGGAACTGGA | 1130 |
rs768571818 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235765286 | CCACTTCTCAATTTA[C/T]CCCTCCTTTCCAGTT | 1130 |
rs768573618 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235855921 | TGTGTTTACTGTTAT[A/G]AAACATTTCACACCA | 1130 |
rs768575056 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817790 | CTGGGTGATGAAATA[C/G]TCTGTACACCAAACC | 1130 |
rs768575443 | snp | C/T | 1.65048e-05 | 0.00287265 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809236 | ATGGGTTTTTGGAAA[C/T]CTGGTTTTTAAAAGC | 1130 |
rs768580511 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235748226 | GAGTGCATGGCAATT[G/T]AAATATATGTCTAGC | 1130 |
rs768584634 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235688512 | TACTTTTGGCTTTCA[C/T]TGAACACGGTGGAGA | 1130 |
rs768594290 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235805025 | AGCATCAGGATTTTT[C/T]AGAGATAAGGCAACA | 1130 |
rs768598173 | snp | C/G | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805843 | ATACTTTGAAGTGAG[C/G]TCTCACTTTCTTGAC | 1130 |
rs768612665 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235666394 | TTCCACTTACATAAA[A/T]TATCTACAATGGGCA | 1130 |
rs768616413 | snp | A/T | 5.16898e-05 | 0.00508353 | intron-variant | LYST | GRCh38.p7 | 1:235775100 | ACCTAAAAAAAAAAA[A/T]GGGTGGATATAGTTT | 1130 |
rs768617972 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235881637 | TGTGTGTGTGTATAT[A/G]TATTTACATACACGT | 1130 |
rs768646807 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235763561 | GTTCAAGCAATTCTC[A/G]TGCCTCAGCCTCCCG | 1130 |
rs768653751 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832947 | TAGGAAGTGGATTTC[C/T]TTTGATATAATAATC | 1130 |
rs768655106 | snp | C/T | 3.54729e-05 | 0.00421132 | intron-variant | LYST | GRCh38.p7 | 1:235697038 | GAAATACTCAAATCT[C/T]ACGAAAGATATATCC | 1130 |
rs768662649 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235667742 | TACAATCTCAGCTCA[C/T]TGCAACCTCCGCTTC | 1130 |
rs768676943 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840677 | GAATTATTTTGAACA[G/T]GTGAGTGGCATGGTC | 1130 |
rs768689963 | snp | C/T | 4.9552e-05 | 0.0049773 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809685 | TGCAGTGTTTTCTTT[C/T]GTCTTGGTGCAAAAG | 1130 |
rs768699011 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235875565 | GGGGCAGCTACATCA[C/T]GCTGATGGAAGGAGT | 1130 |
rs768714665 | snp | A/C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235684176 | AATAGCTATGCTCTT[A/C/G]ATCTGCTTCCTCAAA | 1130 |
rs768726004 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235722092 | AGGATTTCTAAGGAG[-/AA]AAACATTCCAGGCAA | 1130 |
rs768728098 | snp | A/C | 9.91113e-05 | 0.00703888 | intron-variant | LYST | GRCh38.p7 | 1:235709085 | TGTTTTAAAAGAGTC[A/C]CTTACAGCAGGATGA | 1130 |
rs768759954 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235778104 | ACCCAGTTAAATATA[C/T]ATATATATATATATA | 1130 |
rs768768636 | snp | C/T | 4.94491e-05 | 0.00497213 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702928 | ATGGTTTCTAGCGCT[C/T]GTCTCTGAACTGGAT | 1130 |
rs768789539 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665767 | GCAATACCTTATTAA[-/T]TTTTTTCTTTTCAAA | 1130 |
rs768791116 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235790547 | AAATTCTAGTGAAGG[C/T]ATAGTGTCCTAAAAC | 1130 |
rs768791346 | snp | C/T | 1.77109e-05 | 0.00297576 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808404 | CCAATGAAAAAGATC[C/T]AGACATGCTCAACAA | 1130 |
rs768795676 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235798800 | AAAGGAAGTAGATGA[-/G]TGATTGCCAGGGGCA | 1130 |
rs768810140 | snp | C/T | 1.67407e-05 | 0.00289311 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752058 | AGCATTACAATAAGG[C/T]CTTCAATAACCCTAA | 1130 |
rs768812719 | snp | G/T | 1.65638e-05 | 0.00287778 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235762734 | CCTTCATATGGTGAA[G/T]CAGTAAAACCAGATG | 1130 |
rs768828241 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805946 | GCTGTAACTCTAATT[C/T]ACCTAAACTGTCAGC | 1130 |
rs768849788 | in-del | -/A | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884726 | TTTAATATGTCTGTT[-/A]ATGGATTTCTGAATT | 1130 |
rs768850281 | in-del | -/TTT | | | intron-variant | LYST | GRCh38.p7 | 1:235856943 | CAGGATATACTGATT[-/TTT]TTTTTTTTTTTTTTT | 1130 |
rs768851571 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | LYST | GRCh38.p7 | 1:235733711 | ACAAATAATAAGATT[A/G]TCCATAGTTAAGCAT | 1130 |
rs768853432 | snp | C/T | 3.29625e-05 | 0.00405958 | missense | LYST | GRCh38.p7 | 1:235677106 | CTGAATCACACACAG[C/T]AGCAATATCACCTGA | 1130 |
rs768870733 | snp | A/G | 1.66228e-05 | 0.0028829 | intron-variant | LYST | GRCh38.p7 | 1:235788855 | CGCTCTCTATAAGAA[A/G]AAGATGTTAGAATGA | 1130 |
rs768881284 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235771398 | TTCTTTTAAAATCAA[A/G]CAACCCCAAATTTGC | 1130 |
rs768899025 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747178 | ACTGCACCTGCTCCA[A/G]GAGGTACAACACAGG | 1130 |
rs768899960 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235692338 | ACTTCATCTCATAAC[A/C]AACCAACCAACCAAC | 1130 |
rs768925075 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718115 | GTGATCCATCCACCT[C/T]GGCCTCCCAAAGTGC | 1130 |
rs768933363 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235819437 | TCAAACCAAGATCTT[-/A]ATCTCCCAAGTTTTA | 1130 |
rs768951933 | snp | C/G/T | 6.91962e-05 | 0.00588167 | intron-variant | LYST | GRCh38.p7 | 1:235810584 | CAATATGTTTTAAAA[C/G/T]TCAATTTTAAGGTGA | 1130 |
rs768951994 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235846997 | GGCCTTGCTAGAGAC[A/G]TAGACATCCAAATAC | 1130 |
rs768961881 | snp | C/T | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806260 | CAAATGTCTGCTGCT[C/T]GGTGCATATGTTCAG | 1130 |
rs768965824 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235685147 | TCTTTCCTTTACTTA[C/T]AGTAGATTGATCCCT | 1130 |
rs768971124 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235772713 | ACTCCTGGCCAGCAT[A/G]GCTCCCCTAGTTAGA | 1130 |
rs768971947 | snp | C/T | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777101 | TGCCAGTTCCACCAA[C/T]TTCGTGCAGAATGCC | 1130 |
rs768974637 | snp | G/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731098 | AACATCTCTGTAAAC[G/T]TCTCCTCTCTCGATT | 1130 |
rs768986985 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810224 | AGCTTTGGGGTGGTC[C/T]TGTTTAGGAAACGAT | 1130 |
rs768987064 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235733404 | AAATTGTTTAATGAA[A/G]TGATTTTATGAGTCT | 1130 |
rs769006526 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235717095 | ATAACTGATGTTGCT[C/T]GTGGGAGCAGATTCC | 1130 |
rs769014135 | snp | A/G | 1.75311e-05 | 0.00296061 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781031 | GCATACAGATAAAAG[A/G]CCTCTTGTGAACCAA | 1130 |
rs769016433 | snp | C/T | 1.67458e-05 | 0.00289355 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766263 | CATGGGTGTGAGTTG[C/T]CCCTCTTTGTATTCC | 1130 |
rs769023118 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703716 | GTCATCTTCAACTCC[A/G]TTCTCCTCACCACAA | 1130 |
rs769026916 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235848698 | GAAATGGGAGATACT[A/G]CAACTGACACCACTG | 1130 |
rs769033679 | in-del | -/AAGTAT | 2.23003e-05 | 0.00333911 | intron-variant | LYST | GRCh38.p7 | 1:235687100 | AAAGAATGAAACTTA[-/AAGTAT]AATAAAAATAAAATA | 1130 |
rs769040523 | in-del | -/CTC | | | intron-variant | LYST | GRCh38.p7 | 1:235783326 | TTCAATGACATACTT[-/CTC]CTTGACCAAATAAAT | 1130 |
rs769041317 | snp | G/T | 3.29935e-05 | 0.00406149 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806329 | AGCATATGACTTAAA[G/T]GCTCGCTGGCTGTGC | 1130 |
rs769048424 | in-del | -/AT | | | intron-variant | LYST | GRCh38.p7 | 1:235778100 | TTAACCCAGTTAAAT[-/AT]ATATATATATATATA | 1130 |
rs769074788 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235735310 | ACCTATCTTTAGTTT[C/G]TAAGCATTCACTACT | 1130 |
rs769075185 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235880230 | CAATTTCAGAGAAGA[A/C]GGAAGACTATATCTC | 1130 |
rs769086641 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735790 | CAAAAGATGAACATA[C/T]GCAATGGTGAAAATA | 1130 |
rs769094053 | snp | A/G | 1.65154e-05 | 0.00287358 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809580 | CTTTGAAGACAACAG[A/G]TCAGAATCTGAAGAA | 1130 |
rs769094461 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235702525 | GGTTACCGTCTGAAA[C/T]GATGAATTCTTTTTT | 1130 |
rs769106789 | in-del | -/AT | 8.26351e-05 | 0.00642734 | intron-variant | LYST | GRCh38.p7 | 1:235723997 | ATGAGCACTTAAACA[-/AT]ATATATATCAATTAA | 1130 |
rs769141074 | snp | C/T | 4.95659e-05 | 0.004978 | intron-variant | LYST | GRCh38.p7 | 1:235724001 | AGCACTTAAACAATA[C/T]ATATCAATTAATAAG | 1130 |
rs769142815 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702836 | GAAGCTCTCCTTCAA[C/T]ATTGAGCTTGGCTCC | 1130 |
rs769145475 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235815368 | GAAATTATCTAGGAA[A/G]GAGATTACAGAGTGA | 1130 |
rs769152918 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720874 | TTAGGGAGGTTATTT[A/G]TGAGTATATTGTGGT | 1130 |
rs769173142 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235878963 | GTGGTGAGGTCTGGG[A/C]TGTTAGAGTACCCAT | 1130 |
rs769189380 | snp | C/T | 2.21707e-05 | 0.0033294 | intron-variant | LYST | GRCh38.p7 | 1:235693311 | CAGAGTGAGACTCCG[C/T]CTTAAAAATAAATAA | 1130 |
rs769196764 | snp | C/T | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235737905 | CGAAGGTGCTGGAGC[C/T]GCTGCCGACGAGTCT | 1130 |
rs769212842 | snp | G/T | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733870 | TCTGCCAAGCAGCTT[G/T]ATTCACTCCTTCTTC | 1130 |
rs769216073 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235814298 | TAGACAGTAAATATA[C/T]AGATCTGGAACTTAA | 1130 |
rs769220521 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235692755 | TGGGCCAGACACAGT[A/G]GCTCACTGTAATCCC | 1130 |
rs769221909 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235673561 | ACCGAAGGAGTCACC[A/G]CCCCCCACAACTGTC | 1130 |
rs769236915 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235873320 | ATAGAAAAGACTGTA[C/G]TTGTGGGCAACAGTG | 1130 |
rs769239361 | snp | C/T | 1.72466e-05 | 0.00293649 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813056 | TTCTTCTCTACATGT[C/T]AATGCCTATGTCAGT | 1130 |
rs769242570 | in-del | -/TTAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235733183 | TTTGTAATACATATT[-/TTAAA]TTAGTTAGAAAAATA | 1130 |
rs769243375 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769860 | AAAATTCATTAACTA[C/T]TCTTGCTGTTCAAGG | 1130 |
rs769244199 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235785022 | GGCAGACACCATGGA[C/G]TGTAAAGCAATCCAC | 1130 |
rs769249559 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759070 | AACAAGACTTGGCCA[A/G]CGGCCAACAGCTGCA | 1130 |
rs769266670 | snp | C/G | 1.66189e-05 | 0.00288256 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808947 | GATATCTCTGCTCCT[C/G]CTAACTGATCCAAAA | 1130 |
rs769270140 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235843944 | ATTTTCTCAATTCAA[C/T]AGTATTAGAGAAGTT | 1130 |
rs769283933 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235836199 | TCTCATTTTATGTCA[G/T]CAGAAGTTTCATCAA | 1130 |
rs769284838 | snp | G/T | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235792031 | ACACCGTTGCTTAAA[G/T]TTGGAGCGTGCAGTA | 1130 |
rs769290765 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743087 | GGTTTCAGGCATTCA[C/T]CAGGGGTCCTGGAAT | 1130 |
rs769297473 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746405 | CAAGTTCCGTTTCAG[C/T]TGCTTGGCTAGGGTT | 1130 |
rs769307814 | snp | C/G | 3.35723e-05 | 0.00409695 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800385 | AGATTTTTCACAGTT[C/G]CCTGAAGATTAAAAA | 1130 |
rs769308411 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235693134 | TCCTTGCTAACACGA[C/T]GAAATCCCGTCTCTA | 1130 |
rs769309653 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235728660 | AACCCATGTCCCTAC[A/G]TCGTGTTTTAAAATG | 1130 |
rs769310696 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235678486 | CTGAGGGCCACACTG[A/G]CTCACGGATACCAGA | 1130 |
rs769310836 | snp | C/T | 3.32668e-05 | 0.00407827 | intron-variant | LYST | GRCh38.p7 | 1:235729661 | CTTCGATTCACTCTG[C/T]CAAAACATATTTAAA | 1130 |
rs769315348 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235783803 | TAATAACAACTAATA[C/G]AAAGTATTAACTCAT | 1130 |
rs769317170 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791944 | GCCTCTTTCTTGCTC[C/T]GTGAAACTCGTGCTC | 1130 |
rs769324992 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872364 | TGAAGACCGGAAGAC[C/G]CAGGGAAAACTGCCC | 1130 |
rs769337035 | snp | A/C | 0.000149476 | 0.00864381 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809994 | GGAGAATTATGATTC[A/C]AGGTAACGTCAAACT | 1130 |
rs769338051 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235768785 | ATTTCAAAATGGACA[C/T]GCGAAGGAAAAAATT | 1130 |
rs769361065 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant | LYST | GRCh38.p7 | 1:235753284 | TCAAATCTATAATAA[A/G]TAATACAGTTAAGAG | 1130 |
rs769384986 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235669535 | CGATTGGTTGCAAAA[A/G]GCAATCAGATGTTTC | 1130 |
rs769390109 | snp | A/G | 1.82111e-05 | 0.00301749 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780896 | TCCACATCTTTCTTG[A/G]TCATAAAAAGTTCTC | 1130 |
rs769403247 | snp | A/C | 1.73613e-05 | 0.00294624 | intron-variant | LYST | GRCh38.p7 | 1:235804686 | GTAAAATAAAAGAGA[A/C]TAAGAATATTAATAA | 1130 |
rs769407775 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235876503 | GGAAGCTGATGACAC[A/G]GAAGAATATAAATAG | 1130 |
rs769463713 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810104 | GGCAGCTGGCTCACT[C/T]AAAATGTCAGTGTTT | 1130 |
rs769464456 | snp | C/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235734340 | TCACATAGACAAAAG[C/G]AATATAGTATATAGG | 1130 |
rs769475194 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787331 | TGATTCAACCTGTGC[C/T]AGTAAAACAGCTTTC | 1130 |
rs769495026 | in-del | -/A | 5.10452e-05 | 0.00505173 | intron-variant | LYST | GRCh38.p7 | 1:235810559 | GAAAAAAGAAGGCTT[-/A]AGAATACCTCAATAT | 1130 |
rs769503389 | snp | C/T | 5.33661e-05 | 0.00516529 | missense | LYST | GRCh38.p7 | 1:235712150 | ATGAGAGTCGCCAAG[C/T]TGTATTTGTAGAATG | 1130 |
rs769513205 | snp | A/G | 1.6604e-05 | 0.00288127 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808835 | ACTTGAGGAGAGTTC[A/G]GCATCACATAAGTTT | 1130 |
rs769531098 | snp | C/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235750959 | GCAGGGGCAGAATCT[C/G]TGTCTGTTTTTTTCA | 1130 |
rs769551143 | snp | A/C | 3.29549e-05 | 0.00405911 | missense | LYST | GRCh38.p7 | 1:235663987 | AGAAGATCTTACCTG[A/C]TGATGGGCTTATTTG | 1130 |
rs769561565 | snp | A/G | 0.000215002 | 0.010366 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830376 | AAGCCGGTTGACATC[A/G]GTCAGAAATTCACGT | 1130 |
rs769561931 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | LYST | GRCh38.p7 | 1:235686978 | ATCTGTTTGTGTAGG[C/T]TGTGATGACACCGCA | 1130 |
rs769576347 | snp | C/T | 0.000184077 | 0.00959191 | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852971 | TTCTACCTTTCAGAG[C/T]ATTTTAGCGATTAGG | 1130 |
rs769578862 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235694140 | TCAGCCTCCCCAGCA[C/G]CTGGGACTACAGGCG | 1130 |
rs769579628 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804543 | TTCAAAATCTGCTGA[A/G]TAATTCCCGAGGGCA | 1130 |
rs769600064 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235728129 | AATACATTCCACATT[C/T]ACCTGCAGAAAGTAA | 1130 |
rs769607979 | snp | C/G | 1.65168e-05 | 0.00287369 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751165 | ACATAGGAAAGTCAA[C/G]CTAGCCTCAATTTAT | 1130 |
rs769620455 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235753947 | CAATAAGGAGACACA[C/T]GTTTCTCTCTATTCT | 1130 |
rs769627378 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755482 | AACACACTTACTCTT[C/T]ATCAAGGCCAATATG | 1130 |
rs769628356 | in-del | -/T | 0.0156448 | 0.0870496 | intron-variant | LYST | GRCh38.p7 | 1:235762863 | CATCTAGAATCCAAA[-/T]TTTTTTTTGAAACAG | 1130 |
rs769641901 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817199 | CAGTCAGGATGGCTA[C/T]TAAAAATGAAAAAAA | 1130 |
rs769664450 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832511 | CCTAAAATATATACA[G/T]GTTTATATGAATAGG | 1130 |
rs769669619 | snp | A/C | 1.66654e-05 | 0.00288659 | intron-variant | LYST | GRCh38.p7 | 1:235774037 | ATTAGTAATTGGTTA[A/C]TCAGGAAGTTCAACA | 1130 |
rs769688044 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235856257 | TATGGGTTTCTATGA[C/T]GCACAGACATCTTTT | 1130 |
rs769690916 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806583 | AGTACCCACATGTAC[A/G]GAGGACAACTCCTTC | 1130 |
rs769694006 | snp | A/G | 4.95798e-05 | 0.0049787 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830370 | ATTGCAAAGCCGGTT[A/G]ACATCGGTCAGAAAT | 1130 |
rs769698053 | snp | A/G | 1.65586e-05 | 0.00287733 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738560 | ATTAAGCTGTCATGG[A/G]TGAGTCCTTGGGGAA | 1130 |
rs769714211 | snp | G/T | 1.6557e-05 | 0.00287719 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235744056 | CAGAAGACTGTTCAT[G/T]ATGAATATTTTCCTC | 1130 |
rs769715344 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235830101 | CCACTTTTTTTTTAG[C/T]GGAATAATGTGAAAG | 1130 |
rs769720681 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687443 | TATTTTCCTCGTTTT[A/G]TGTCTTTGGTGGGGA | 1130 |
rs769733448 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235781634 | TAAGTTAATATGAGC[-/T]TCTCTTTTTTGAGGA | 1130 |
rs769744103 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235817675 | ACCTTGGGTACACAT[A/G]GACACAAAGAAGGGA | 1130 |
rs769753019 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720674 | ACCTGTATATCAACA[C/G]ATCATTGAGGTCAAG | 1130 |
rs769758903 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235674681 | GATGGCTTAGGAAAA[C/T]AGAATAGCCCTTAAC | 1130 |
rs769761620 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235877277 | CACTCACTCTACCAG[C/G]TGTTTGCTGGAGCCT | 1130 |
rs769787551 | snp | C/T | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734627 | GTGATTATGTATCAA[C/T]TCTGACAAATACAAA | 1130 |
rs769794793 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235706501 | AGGTTTAACTACTTG[A/G]GGTCTTATTTCCACG | 1130 |
rs769831533 | snp | C/G | 1.65567e-05 | 0.00287716 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808608 | CCTCTTTGGAGCACA[C/G]GATTAAATATGTAAT | 1130 |
rs769840460 | snp | G/T | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806058 | CTTAGGTTGAGAAAT[G/T]CTGTTTAAATCCTGG | 1130 |
rs769871824 | snp | C/G | 2.13136e-05 | 0.0032644 | intron-variant | LYST | GRCh38.p7 | 1:235697300 | AAAATAAAAAGTATG[C/G]CTTTTTAAAAGGTGG | 1130 |
rs769874603 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235696685 | CGTGTCTTTAAAACC[C/T]ATTTTCAAGGCTATC | 1130 |
rs769908105 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon | LYST | GRCh38.p7 | 1:235677140 | TTCACTGGCAGAGAC[A/G]GCTGTGACAGGGCTT | 1130 |
rs769914861 | in-del | -/TGT | | | intron-variant | LYST | GRCh38.p7 | 1:235730608 | GTGTGTGTGTGTGTG[-/TGT]GTGTATATGTAAACT | 1130 |
rs769915731 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731176 | GGTCATACCATACTG[C/T]TCTGCAAGTAAAAAG | 1130 |
rs769928217 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235805964 | CTAAACTGTCAGCAC[C/T]CTTTTTTAGACTACC | 1130 |
rs769928421 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235803919 | AGGACAGATGGCAAC[C/T]AAAGGTAAAATAAAC | 1130 |
rs769932143 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235664735 | TTTATTGATGAAGTT[G/T]GTAGACAACCCATGA | 1130 |
rs769942827 | snp | C/G | 3.2969e-05 | 0.00405998 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810355 | TTCTTGCATCTCTTA[C/G]AGAATAGCGATGGGT | 1130 |
rs769955560 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235762049 | TAATGGGTGCAGCAC[A/C]CCAACATGGCATATG | 1130 |
rs769964867 | snp | C/T | 1.66468e-05 | 0.00288498 | intron-variant | LYST | GRCh38.p7 | 1:235800311 | TTGTTTAAAACAGTT[C/T]CAACTTACCTTGAAA | 1130 |
rs769966311 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235842309 | CCAGACTGAAGAGTA[C/T]ACAATGTGGGAATGA | 1130 |
rs769999880 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235747023 | AAAGTGAAGAGATCA[C/G]GAAGGTGAATATAAT | 1130 |
rs770002477 | snp | A/G | 1.65351e-05 | 0.00287528 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777111 | ACCAATTTCGTGCAG[A/G]ATGCCTTGAATAGTT | 1130 |
rs770004763 | snp | A/G | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810417 | ACATTTACTTTTGCA[A/G]AAACCTGACTAGACA | 1130 |
rs770017837 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235788062 | TTAAGACCATTACAA[A/T]CTGATAGAATATTTC | 1130 |
rs770018136 | snp | C/T | 0.000115623 | 0.00760251 | intron-variant | LYST | GRCh38.p7 | 1:235724005 | CTTAAACAATATATA[C/T]CAATTAATAAGGGTG | 1130 |
rs770034004 | snp | C/T | 3.29717e-05 | 0.00406015 | intron-variant | LYST | GRCh38.p7 | 1:235677474 | TTTGGAGACCTTCTT[C/T]TGTACCTGTTTAAAT | 1130 |
rs770050385 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235763395 | ATGTGGTAACCTGGA[G/T]CTACCCTTGACCACT | 1130 |
rs770084241 | snp | C/T | 5.46115e-05 | 0.0052252 | intron-variant | LYST | GRCh38.p7 | 1:235773793 | GTAAATTTTGTGTTA[C/T]ATGCATTTTACCACA | 1130 |
rs770085753 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759167 | GCCAATCCCTTTAGG[C/T]AATCAGGTCGGCGTG | 1130 |
rs770087096 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809164 | ACTGATGGGCACACA[C/G]TGCAATGCAACAGCA | 1130 |
rs770096789 | snp | A/G | 3.31285e-05 | 0.00406978 | missense, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766097 | TGTGCAAAGAAAAGT[A/G]GAAGTTCGTGGGATT | 1130 |
rs770104371 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235790203 | AAGAGACTGTTTACA[C/T]TGAGATTGCCTCCAT | 1130 |
rs770104760 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235771226 | AAATCTGAAAAGTAG[C/T]ACCAAGATAAAATAG | 1130 |
rs770106698 | snp | A/G | 1.64849e-05 | 0.00287092 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662927 | CTTTGGAGAACGTGA[A/G]GTTCATTCGCATTCA | 1130 |
rs770117943 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235695487 | GAACATAGCTATTAA[A/G]GGCACACTAAGGGTT | 1130 |
rs770120308 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235862237 | TTTAAATGACCAATT[C/T]GCTTTTTCTTTTCTG | 1130 |
rs770130104 | snp | C/T | 1.65345e-05 | 0.00287524 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235716731 | TATGTGTCCACATAA[C/T]GATCTTCTTTTTCTT | 1130 |
rs770138410 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235870169 | TGGGGGGTGTGGGGA[A/G]GTGGGTGGCATTGGT | 1130 |
rs770155992 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235671800 | TATGTAAATGGGAAG[C/T]AATTAGATTAAGAAG | 1130 |
rs770160558 | snp | A/G | 1.65263e-05 | 0.00287452 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235803001 | AACTACAACACTGAG[A/G]ATCCTCAGCTTCTTC | 1130 |
rs770175695 | snp | C/T | 3.30376e-05 | 0.0040642 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759075 | GACTTGGCCAACGGC[C/T]AACAGCTGCAGATCC | 1130 |
rs770179141 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235731556 | ATTTCCCATTTTGCA[-/T]TTTTTTTTTTTTTTT | 1130 |
rs770196370 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756630 | TGGGTTGTTTTCTAA[C/T]GGAAACTATTCATAT | 1130 |
rs770207658 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235696775 | TTTGTTGGTCAAATA[C/T]GTCTGTCTATTCTGG | 1130 |
rs770219010 | snp | G/T | 1.65015e-05 | 0.00287237 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702946 | CTCTGAACTGGATCT[G/T]CAACTGCAGAGACAT | 1130 |
rs770230096 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869380 | GAGAGGCTGAGGCAG[A/G]AGAATAGCGTGAACC | 1130 |
rs770246867 | snp | C/G/T | 3.2961e-05 | 0.00405951 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734488 | ATTGACTCACCTCTT[C/G/T]GATCATTTTAATAAG | 1130 |
rs770253046 | snp | A/G | 1.66663e-05 | 0.00288667 | intron-variant | LYST | GRCh38.p7 | 1:235788869 | AAAAGATGTTAGAAT[A/G]ATCAGTAAAATGGTT | 1130 |
rs770253107 | snp | A/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235716908 | TTTCTCTGCTTAAAC[A/G/T]TATTGTTTTGTAACT | 1130 |
rs770255593 | snp | C/G | 1.66087e-05 | 0.00288168 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753105 | AGAGTAGACCATTAT[C/G]CAGCAACATATCTGC | 1130 |
rs770266500 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235786355 | CACAATGAGATACCA[C/T]CTCACACCAGTTAGA | 1130 |
rs770276682 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808464 | ACAAACCTGGATTTA[A/G]GCAGGATAGGCAGAG | 1130 |
rs770326654 | snp | A/G | 2.50768e-05 | 0.00354087 | intron-variant | LYST | GRCh38.p7 | 1:235830188 | ACAGTTAACTATCAT[A/G]TATTGATGAAAGTAA | 1130 |
rs770331918 | snp | C/T | 4.94629e-05 | 0.00497283 | missense | LYST | GRCh38.p7 | 1:235709111 | GATGAAAAACATTGA[C/T]CGCTTGAACAGAAGC | 1130 |
rs770348264 | snp | C/T | 1.6659e-05 | 0.00288604 | intron-variant | LYST | GRCh38.p7 | 1:235724195 | TCTAAGACAAAGAAA[C/T]AGGCAAAAATATTTG | 1130 |
rs770359262 | snp | C/G | | | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235826456 | AAATTAAAAAGTAGT[C/G]AACTACTGAATTATG | 1130 |
rs770360969 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822133 | GATAGAGACAGCTCA[A/G]AATGAAAAAAGGCCT | 1130 |
rs770362521 | snp | G/T | 3.3048e-05 | 0.00406484 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809692 | TTTTCTTTTGTCTTG[G/T]TGCAAAAGGGTCAGG | 1130 |
rs770367384 | in-del | -/C | 1.65776e-05 | 0.00287898 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741387 | TTGTATTTCACCAAA[-/C]GTTTTACTTCTCTTA | 1130 |
rs770379680 | snp | C/T | 1.74558e-05 | 0.00295425 | intron-variant | LYST | GRCh38.p7 | 1:235775119 | TGGATATAGTTTTCT[C/T]CCAATTTGCTGAGAG | 1130 |
rs770380080 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847096 | TATCCAAAGTTAAGA[C/T]GAAGGAAAGAATTTT | 1130 |
rs770391160 | snp | A/G | 1.71434e-05 | 0.0029277 | synonymous-codon, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752171 | TTCACTCATGGGAAT[A/G]CTAAAGATAACAACA | 1130 |
rs770405718 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755600 | ACGATTCTTCAGAAA[C/T]TTATCTTTTTGTTCC | 1130 |
rs770423357 | snp | A/G | 3.30017e-05 | 0.00406199 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806334 | ATGACTTAAAGGCTC[A/G]CTGGCTGTGCTGTCA | 1130 |
rs770437860 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235691857 | TGCCCACCACCATGC[A/G]TGGCTAATTTTTGCA | 1130 |
rs770444642 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235798663 | AATTTAAAAAATGAT[C/T]AGAAAGAGAACTAAA | 1130 |
rs770455300 | in-del | -/G | 1.65091e-05 | 0.00287303 | intron-variant | LYST | GRCh38.p7 | 1:235728029 | AATTGATACATTTTT[-/G]GAATCTGTCTAGATT | 1130 |
rs770465715 | snp | A/G | 1.66048e-05 | 0.00288134 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808964 | TAACTGATCCAAAAT[A/G]AGTTTGTTAAGGATA | 1130 |
rs770465776 | snp | A/C | 1.64795e-05 | 0.00287045 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810204 | GTTGCTAAGCGGTCA[A/C]GTTTAGCTTTGGGGT | 1130 |
rs770469836 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715255 | TGACCAGGAAGTGAA[A/G]CACAGTGCCGCTATT | 1130 |
rs770486687 | snp | C/T | 8.24246e-05 | 0.00641915 | intron-variant | LYST | GRCh38.p7 | 1:235693518 | AAGAAAAGTATCAGA[C/T]TGTCACTGCTCGACT | 1130 |
rs770489247 | snp | A/G | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235751062 | AAAAGCACTAAAAGT[A/G]AGGAGCAGAATAGTT | 1130 |
rs770495236 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235783638 | ATGTATCCCAGAACT[A/G]AAGTAAAATAAAAAT | 1130 |
rs770501203 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235839677 | CCATGTGCGGTGGCA[C/T]CGCCTATAGTCCCAG | 1130 |
rs770504406 | snp | C/T | | | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739663 | GTTGACAAGGGAAAG[C/T]TCTTCCCTATAGTAA | 1130 |
rs770510261 | snp | C/T | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746437 | TCTTGGCTCATTCTC[C/T]GTTGCATCATCACAT | 1130 |
rs770511908 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235875101 | TCCCTCCATTCCTAG[A/G]ATAGAGGGAACAGCG | 1130 |
rs770523581 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819819 | CCCAGCTAATCTTTT[C/T]GTAATTTTAGTAGAG | 1130 |
rs770537189 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235814228 | ATGGATTCACTTTTC[A/G]GACATATGGAGTCTG | 1130 |
rs770540766 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235683793 | CAGAAACCAGTGAAC[A/G]TGAGGTGTCTCCTGC | 1130 |
rs770554506 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235882251 | GCTGAGGGAATAGCA[C/T]AGGAAGTAAGGAGGC | 1130 |
rs770565119 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676724 | AAATTTTGTTCTTTC[A/T]CAGGAGGAAGGTAAC | 1130 |
rs770580160 | in-del | -/T | | | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235884606 | CAAACTCCTAGTGTC[-/T]TTTTTTTTTTTTTTT | 1130 |
rs770588600 | snp | A/T | 3.29859e-05 | 0.00406102 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809061 | ACAGATTTGGGATCC[A/T]TACAACAGCATATTC | 1130 |
rs770591122 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235854009 | TATGAAGGTTCATCC[A/G]GGTAAATCATCTCCC | 1130 |
rs770608330 | snp | G/T | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235741256 | CAGAGGTTAAATTGA[G/T]CCTGTGTGAAAGCAC | 1130 |
rs770621339 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235813673 | ATACATACACATAAA[C/G]AGTTAAAGAACAGCA | 1130 |
rs770632046 | in-del | -/AC | | | intron-variant | LYST | GRCh38.p7 | 1:235857706 | GGTGTATATATATAC[-/AC]ACACACACACGTATA | 1130 |
rs770636769 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806276 | GGTGCATATGTTCAG[A/G]AGAAGGCAAGACAAG | 1130 |
rs770638775 | snp | C/T | 4.98227e-05 | 0.00499088 | missense | LYST | GRCh38.p7 | 1:235693351 | AATAAAGTGTTTACC[C/T]GGTACTGTTGTGAAC | 1130 |
rs770660425 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235698496 | AGACGTTAGGGTCAG[C/G]CATTTTGAAAACAAG | 1130 |
rs770662078 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235767164 | TATATCCTCCAATTC[C/T]ATCTCCCCAGTGGGT | 1130 |
rs770679237 | in-del | -/CTT | 0.000181943 | 0.00953616 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235802962 | TATCTGCTTCGTAAC[-/CTT]CTTCTTCAACTAAAA | 1130 |
rs770686007 | snp | A/T | 1.6513e-05 | 0.00287336 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235733892 | TCCTTCTTCAGTTTC[A/T]TATTTCTTTTGTTCC | 1130 |
rs770714403 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738578 | AGTCCTTGGGGAACA[C/T]GGAGATTCTAGTGTG | 1130 |
rs770718384 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838608 | TACATTTTTTTAAAT[G/T]TTAGAACATTATTCC | 1130 |
rs770719390 | snp | A/C | 3.96267e-05 | 0.00445104 | intron-variant | LYST | GRCh38.p7 | 1:235774872 | ACGAGATGAGTATCA[A/C]TGCATATGAAACTAT | 1130 |
rs770736222 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791950 | TTCTTGCTCCGTGAA[A/G]CTCGTGCTCTTCTCA | 1130 |
rs770747189 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759413 | CTCCCCAAAGAATTT[C/T]GTTTCTTTGATTGGG | 1130 |
rs770773468 | in-del | -/AA | | | intron-variant | LYST | GRCh38.p7 | 1:235720174 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 1130 |
rs770775963 | snp | A/G | 1.82503e-05 | 0.00302073 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746513 | CAGTTTGAGCAAGGG[A/G]AAATTTTCGAGGACC | 1130 |
rs770777983 | snp | C/T | 1.65207e-05 | 0.00287404 | intron-variant | LYST | GRCh38.p7 | 1:235733726 | GTCCATAGTTAAGCA[C/T]ACATGGAACGTATTT | 1130 |
rs770783736 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235804480 | TCATACCCAAAGAAC[A/G]CAACTATATGTTGTT | 1130 |
rs770786132 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235726704 | ACACATTTATAGCAT[C/G]CAAGTTGACTTAAAA | 1130 |
rs770806309 | snp | C/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853115 | AACTTCTTGCCCCCC[C/G]ACAAACTTCTCAAGA | 1130 |
rs770811951 | snp | C/T | 0.000217448 | 0.0104248 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759574 | GGCGGCCATCTGTTG[C/T]GGAATAATATTAGAG | 1130 |
rs770824967 | snp | G/T | 1.65553e-05 | 0.00287705 | intron-variant | LYST | GRCh38.p7 | 1:235804696 | AGAGACTAAGAATAT[G/T]AATAACCATTTTAAA | 1130 |
rs770837885 | snp | C/G | 8.24341e-05 | 0.00641952 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810123 | ATGTCAGTGTTTGAC[C/G]CCTGTCTTGGAATAA | 1130 |
rs770839969 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235750726 | TTTAATATCTGAATG[A/C]ACTGTTTCTTCTTTA | 1130 |
rs770843989 | snp | C/T | 9.89903e-05 | 0.00703458 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235730911 | AATGAGTTTTGTCTT[C/T]AAACAGGTAAGAGAG | 1130 |
rs770844088 | snp | A/G | 0.000147721 | 0.00859295 | synonymous-codon | LYST | GRCh38.p7 | 1:235712181 | AAAAGTTCTGTCTGG[A/G]ATGTCAAAACTTTGA | 1130 |
rs770846589 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235737087 | GGTTGAAGTTGGCAG[C/T]CTGACCAAATAAAGA | 1130 |
rs770848057 | snp | C/G | | | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866111 | GGACCATTAAACAAC[C/G]CCTTCGTTGGGCTTT | 1130 |
rs770855731 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235696802 | CTGGGGCTCAACAGC[C/G]TCAAAGTGTACATTT | 1130 |
rs770871242 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235880627 | TTTTTACCAAGAGTA[-/T]TTTTTTCTATTCTTG | 1130 |
rs770873283 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235775504 | ATAAAAACCACATGT[C/T]CTGCCTTGTATGTCA | 1130 |
rs770875567 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698930 | TGAGAAAAATGTGTG[C/T]GCTAAATTTTAGTTA | 1130 |
rs770877524 | snp | A/G | 1.65332e-05 | 0.00287512 | intron-variant | LYST | GRCh38.p7 | 1:235733497 | AACTGACCTCCCGCA[A/G]CTTACCTATCATGTG | 1130 |
rs770885913 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235735732 | ACATTTTGGGTGATA[C/T]TTAAATTAACATGCT | 1130 |
rs770889813 | in-del | -/T | 1.64825e-05 | 0.00287071 | frameshift-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235787224 | AGACCCATATGGAGA[-/T]TTTTCCCATGAATCC | 1130 |
rs770890620 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | LYST | GRCh38.p7 | 1:235702801 | GAAAGCAAACTGCAC[G/T]AGCAACCCCACAGCA | 1130 |
rs770896926 | snp | A/T | 1.64836e-05 | 0.0028708 | missense | LYST | GRCh38.p7 | 1:235664038 | CTCACAGGCTTTAAG[A/T]CCCATGTGCTCCATA | 1130 |
rs770952649 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235719407 | TTGTCTATTTTCTTC[C/T]AATAAATTTAGAAGA | 1130 |
rs770961259 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235760408 | TTTTTGCAGTCACTT[C/T]TTGCTGTTATTAGTG | 1130 |
rs770962889 | snp | G/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810435 | ACCTGACTAGACAGG[G/T]CACTTCCTTCTAAAT | 1130 |
rs770969479 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806143 | CTGAACAGTTTCTGT[A/G]TTATCATAAATATTA | 1130 |
rs771001554 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235710297 | AGCTCAGCAGTCATC[A/G]TACAGAGCAGCTGCA | 1130 |
rs771002043 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235850463 | TTTCTAGACATTGGC[G/T]TAGGCAAGGATTTCA | 1130 |
rs771004545 | snp | C/T | 1.67823e-05 | 0.0028967 | intron-variant | LYST | GRCh38.p7 | 1:235716782 | TTAGAGAGATTTCTG[C/T]AAGAAAAGGACAATT | 1130 |
rs771007594 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235687115 | AAGTATAATAAAAAT[A/G]AAATAAAAGAATGAA | 1130 |
rs771009066 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793736 | ATAAAAAATCTAGTA[G/T]AGGAATCACAAAATT | 1130 |
rs771017119 | snp | A/G | 3.32486e-05 | 0.00407715 | synonymous-codon | LYST | GRCh38.p7 | 1:235664494 | TTCTAATCCCCCAGC[A/G]ATTACATTGATAGAT | 1130 |
rs771020498 | snp | G/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661352 | AATTTAAAGTTCTCA[G/T]TAAAAAAATGAAAGC | 1130 |
rs771034041 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235877363 | AATATAGGAATCATG[C/G]GAACACAGAATTCAT | 1130 |
rs771053964 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235832816 | TCATAAGGTAGGTTT[C/T]ACATATTTCTTGTTA | 1130 |
rs771060529 | snp | A/T | 1.66161e-05 | 0.00288232 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235800322 | AGTTTCAACTTACCT[A/T]GAAAATCAGAATCAT | 1130 |
rs771073257 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720686 | ACAGATCATTGAGGT[C/T]AAGTGTCTCACTAAC | 1130 |
rs771074733 | snp | A/C | 4.96307e-05 | 0.00498125 | intron-variant | LYST | GRCh38.p7 | 1:235757465 | TCAGTTACACTAAAA[A/C]AGAGACCAAAAAAGT | 1130 |
rs771076437 | snp | C/T | 1.66635e-05 | 0.00288643 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235766240 | AATGATCTACAAACC[C/T]CTCGGGGCATGGGTG | 1130 |
rs771076972 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235816581 | TAAAATTCATATGGA[A/G]TAAGAAAAGACTCTG | 1130 |
rs771096844 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235795231 | CTGTTTCTCAGTACA[C/G]AGCACAGATAGTTCA | 1130 |
rs771118540 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235751284 | GAATCTGTGAGGTTT[C/T]CAGAGTCATGATTTG | 1130 |
rs771144610 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235874992 | GCTTGAGAGAAATGC[A/G]GAATCTCAGGCCATG | 1130 |
rs771145198 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235665421 | TCGAGACCAGCCTAG[C/T]TAACATGGTGAAACC | 1130 |
rs771161678 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235837485 | ATACAAAAATTAGCC[A/G]GCATGGTGGTGCACA | 1130 |
rs771166512 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235822441 | CTCATTATTGTATAT[A/G]GGGCATATGCGGAGC | 1130 |
rs771166808 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235817545 | AGCCACAAAAAAGAA[G/T]GAGATCATGTCCTTT | 1130 |
rs771180171 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235761849 | GCCTTTTTTCAGCAT[A/G]TCAGAACTCCCCCAA | 1130 |
rs771182641 | in-del | -/A | 6.87959e-05 | 0.00586457 | intron-variant | LYST | GRCh38.p7 | 1:235744168 | AAATTCTTTGAATTG[-/A]AAAAAAGAATACAAA | 1130 |
rs771210216 | snp | C/T | 1.67242e-05 | 0.00289168 | intron-variant | LYST | GRCh38.p7 | 1:235791663 | ATAGTCTGAAAACAA[C/T]CTTTGTGTACAAATC | 1130 |
rs771230485 | snp | A/C | 3.31928e-05 | 0.00407373 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753110 | AGACCATTATCCAGC[A/C]ACATATCTGCTACCT | 1130 |
rs771237392 | snp | A/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662691 | CATTTTAATGTACCA[A/T]GCGAGGCTTAAAACT | 1130 |
rs771253823 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235847589 | GGCCTAAATGCTCCA[C/T]TTAAAAGATACAGAA | 1130 |
rs771255150 | snp | C/T | | | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235867434 | GCCTTCCTCTGGGAC[C/T]TGGAAAAAGCCATAT | 1130 |
rs771256800 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235838013 | CGAAGAAGACCAACA[A/T]ACAAGTGGAAGGAAC | 1130 |
rs771271251 | in-del | -/GAG | | | intron-variant | LYST | GRCh38.p7 | 1:235837841 | AACGGGTGATGGCTT[-/GAG]GAGGACATGAGATAA | 1130 |
rs771274608 | in-del | -/TATC | 1.65037e-05 | 0.00287256 | intron-variant | LYST | GRCh38.p7 | 1:235730973 | AGTAAATATTATCTT[-/TATC]TAATGACCATAGTTC | 1130 |
rs771274641 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | LYST | GRCh38.p7 | 1:235702717 | TCTAATCAGGTTTTG[C/T]TGCACTCGATTGAAA | 1130 |
rs771279036 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235858854 | TTTCTGCATTGTTAT[C/G]GGGGGCAGGGAAGGG | 1130 |
rs771281143 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235843692 | ACTGAAAAAAAAAAT[A/T]GGAAGTCCCTGTATT | 1130 |
rs771284160 | snp | A/G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235822968 | ACTGCAAACTCAGAT[A/G/T]TAAGACCAGCTGATA | 1130 |
rs771319070 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791843 | CTTCTGATAGGTGTG[A/G]CCAGCAGTTTTGCCC | 1130 |
rs771326858 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235883149 | GCTGCCCATGCTCTC[A/G]GCTGGCACTGAAAAG | 1130 |
rs771332220 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235706172 | TGCATTTATTTTATA[C/T]TTGATGGAGTTTAGG | 1130 |
rs771334221 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235693581 | GGGTGAAGTTTACAT[A/G]GCAGAACATATCATT | 1130 |
rs771344080 | snp | A/G | 1.66192e-05 | 0.00288259 | intron-variant | LYST | GRCh38.p7 | 1:235758968 | TACAAAAACACATAA[A/G]TACCTGTGAGCACTT | 1130 |
rs771372992 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235857719 | TACACACACACACGT[A/G]TATATACACAAACAT | 1130 |
rs771379538 | snp | A/G | | | intron-variant, utr-variant-5-prime | LYST | GRCh38.p7 | 1:235865244 | GTCTTGGCTCAAATG[A/G]TATCTTTTCTAGGAA | 1130 |
rs771400826 | snp | C/T | 0.000462168 | 0.0151944 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806077 | TTTAAATCCTGGTTT[C/T]CATTTACACTTGTAT | 1130 |
rs771416000 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235837349 | CTGAGAGAAAGCTGG[C/T]GGGTGCAGTGGCTCA | 1130 |
rs771431448 | in-del | -/TT | 1.85534e-05 | 0.00304571 | intron-variant | LYST | GRCh38.p7 | 1:235791599 | AAGGTGAAGAACATG[-/TT]TTAAGAGTGTTAAGA | 1130 |
rs771432389 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235760070 | GGTTCTACTGTGCTG[-/A]ATTTAAGTGAATTAA | 1130 |
rs771447925 | snp | A/G | 3.29919e-05 | 0.00406138 | intron-variant | LYST | GRCh38.p7 | 1:235731186 | TACTGCTCTGCAAGT[A/G]AAAAGATTAAAGGGT | 1130 |
rs771449949 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235689991 | TCATCTTTGTCCTCT[C/T]TTCACACCACATCAA | 1130 |
rs771452304 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235869561 | GTCTTCAGCTAATTT[A/G]ACTCCAGAATTATAA | 1130 |
rs771462669 | snp | A/G | 1.65853e-05 | 0.00287964 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809855 | CATCCTTTGAATCAA[A/G]GCCACCGGTTCTTCG | 1130 |
rs771480883 | snp | C/T | 1.68579e-05 | 0.00290321 | missense | LYST | GRCh38.p7 | 1:235709264 | AAGGGGGAAGGTTGA[C/T]GTGATTAACCCGTTC | 1130 |
rs771513596 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777238 | TTCATTTGACCTTTA[A/G]GTCTAATCACTGGTT | 1130 |
rs771540109 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235881748 | ATCTTGAAGGTATGC[C/T]GCTGAGTGAAAAAAG | 1130 |
rs771549954 | snp | C/G | 3.48438e-05 | 0.00417381 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235812976 | AAAAGCATACCTGTT[C/G]CCTTTTCTTCTTGGA | 1130 |
rs771566362 | snp | C/T | 0.000164271 | 0.00906138 | intron-variant, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747258 | GAAGGAGAAGGGCAT[C/T]GGAAGTTGACCATAG | 1130 |
rs771566931 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235769870 | AACTATTCTTGCTGT[A/T]CAAGGCAGTACAAAA | 1130 |
rs771583567 | snp | C/G | 1.65985e-05 | 0.00288079 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808639 | TATATAATTTCCACT[C/G]AACAACTATATTGCC | 1130 |
rs771595479 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235671395 | TCTTTTGAGATTATC[A/C]TATGGCTTTTGCTCT | 1130 |
rs771612633 | snp | C/T | 0.000263835 | 0.0114825 | intron-variant | LYST | GRCh38.p7 | 1:235693529 | CAGATTGTCACTGCT[C/T]GACTGTTACATGACA | 1130 |
rs771619130 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235861075 | TCTGTTATATAAACA[C/T]TGCTTTTTAAAGATG | 1130 |
rs771619563 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235701400 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCATGAGG | 1130 |
rs771633189 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235797011 | TGAAGAAATTAGAAC[C/G]CTTATACACTGATGG | 1130 |
rs771634926 | snp | A/G | 3.30017e-05 | 0.00406199 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806358 | GCTGTCATAGCCAGA[A/G]GTATCTTCTGAGTCA | 1130 |
rs771649407 | snp | A/G | 1.64958e-05 | 0.00287187 | missense | LYST | GRCh38.p7 | 1:235663056 | CTGTGTACAAATGGT[A/G]GCCATCACAAGAAAA | 1130 |
rs771656843 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235770826 | CATGATTACAAACTA[C/T]GCACTTCAAAGAGTA | 1130 |
rs771658183 | snp | A/C | 1.65315e-05 | 0.00287498 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235773916 | GGATTATAGCATTAG[A/C]GTCTACATCCAACTT | 1130 |
rs771658403 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235862594 | TGAGGTCAGCAGTTC[A/G]AGACCAGCCTGGGCA | 1130 |
rs771660253 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235833197 | CTAACAGAAATATTG[A/T]ATTTAATTGAATGAC | 1130 |
rs771662965 | snp | C/T | 1.74436e-05 | 0.00295322 | intron-variant | LYST | GRCh38.p7 | 1:235733917 | TGTTCCTAGAAGATT[C/T]AGATAATAATATACT | 1130 |
rs771676168 | snp | C/T | 6.63438e-05 | 0.00575912 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235803056 | CAATTCTTCTGCAGA[C/T]TGATGACTCTATAAA | 1130 |
rs771677157 | snp | A/G | 6.59696e-05 | 0.00574286 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809143 | CCTGCTGTAGTAAGC[A/G]CAAGCACTGATGGGC | 1130 |
rs771692840 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235858753 | ATCACATCTTCCCTT[A/C]CAATCTCAATCCAGG | 1130 |
rs771702126 | in-del | -/GCCCAGC | | | intron-variant | LYST | GRCh38.p7 | 1:235863112 | AAAATCTTGAACTTG[-/GCCCAGC]ACGGTGGCTCACGCC | 1130 |
rs771704807 | in-del | -/GCC | | | intron-variant | LYST | GRCh38.p7 | 1:235755778 | AAAGCTTAAAAAAAT[-/GCC]GCCACCACCACAGCA | 1130 |
rs771707827 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235688611 | CACAACATGAAGGCA[A/C]ACAGCCGTCAGGACT | 1130 |
rs771710044 | snp | A/C/G | 0.000148787 | 0.00862399 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235781978 | CAGCCAACTGCAAAA[A/C/G]CTCTTCTTGGGATGA | 1130 |
rs771729441 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235841923 | TAATTATTGGAAGAA[C/T]AGTCAAATGGGGGAA | 1130 |
rs771739483 | in-del | -/T | 3.36604e-05 | 0.00410232 | intron-variant | LYST | GRCh38.p7 | 1:235677224 | ATTTGTATATGATCA[-/T]TAAATATAATTACAT | 1130 |
rs771746684 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235789551 | AAAGCTATGTTATGA[C/T]ATATCAAAATCCAAA | 1130 |
rs771747212 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235756264 | CACACATCTATTTAT[A/T]CCCCTACTAAAAAAG | 1130 |
rs771779306 | snp | A/G/T | 6.59245e-05 | 0.00574097 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662936 | ACGTGAAGTTCATTC[A/G/T]CATTCACCCGGCTGC | 1130 |
rs771794522 | snp | C/T | 1.66352e-05 | 0.00288398 | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235762707 | GTCATACTTCCATTA[C/T]TGCTATTTTTACCTT | 1130 |
rs771795466 | snp | C/T | 1.64909e-05 | 0.00287144 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759175 | CTTTAGGTAATCAGG[C/T]CGGCGTGGGCAGGAC | 1130 |
rs771818821 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235782292 | TCCTGCCTCAGCCTC[C/G]CAAGTAGCTGGGATT | 1130 |
rs771827282 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235850893 | GATGTTGGCATGGAC[A/G]TGGTGAACAGGGAAC | 1130 |
rs771833094 | snp | C/G | 1.65384e-05 | 0.00287557 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809707 | GTGCAAAAGGGTCAG[C/G]CTGCTTTTCTAGGCA | 1130 |
rs771837929 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235772791 | AGTCTCCCCTTTCAG[A/G]GTTTATGGTAAATGC | 1130 |
rs771845290 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235876418 | CTAAGTTGTGGGAAC[G/T]GCATTTTGACTTTTT | 1130 |
rs771845910 | snp | A/C/G | 3.29828e-05 | 0.00406085 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809081 | ACAGCATATTCCAAT[A/C/G]TTATGAACACCCGAT | 1130 |
rs771853138 | snp | A/G | 0.000183372 | 0.00957353 | intron-variant | LYST | GRCh38.p7 | 1:235830197 | TATCATATATTGATG[A/G]AAGTAAGTATTTGAT | 1130 |
rs771876940 | snp | C/T | 3.90396e-05 | 0.00441795 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235746521 | GCAAGGGGAAATTTT[C/T]GAGGACCTTTAAAAG | 1130 |
rs771882274 | snp | C/T | 0.000169658 | 0.00920871 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235759595 | AATATTAGAGGAATT[C/T]TCTCCTGGTAAGAGT | 1130 |
rs771884483 | snp | A/C | 1.67607e-05 | 0.00289483 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235775084 | GCTACTGAGTTCAAC[A/C]ACCTAAAAAAAAAAA | 1130 |
rs771888559 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235708288 | TAGTCTGTATTTTAT[A/G]CATTTTTCTAACAAA | 1130 |
rs771897075 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235767110 | TTGGCAAAATGCCAA[C/G]TAATTACTAAAAATA | 1130 |
rs771907395 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731074 | GATACTTATTTGGAA[C/T]AGTTAAATAACATCT | 1130 |
rs771914715 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235734492 | ACTCACCTCTTTGAT[C/T]ATTTTAATAAGGTCT | 1130 |
rs771920312 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235724763 | AATGTCATATAGTTC[C/G]AATTATACAGTATAT | 1130 |
rs771922734 | snp | A/C | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235740850 | CATGGTGACAAGTTA[A/C]ATATATGTTTAATTT | 1130 |
rs771931051 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235875327 | TTAACTAAGGCATGT[C/T]CCATGTTGCTTAAAA | 1130 |
rs771955142 | snp | C/T | 1.67579e-05 | 0.00289459 | intron-variant | LYST | GRCh38.p7 | 1:235664641 | AACACCCAAATCATC[C/T]GGCGGGTTACCAGAA | 1130 |
rs771956861 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235840034 | AGGAACTCTGTACTC[C/T]AATTCTCTATATTCC | 1130 |
rs771966734 | snp | C/T | 1.65905e-05 | 0.0028801 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235755640 | CTAGCAAAATATGCA[C/T]CTAATAGCTAAACAA | 1130 |
rs771978184 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819098 | GGCAAGTGCAGATGT[C/T]TGGGTTTTGGCCCCT | 1130 |
rs771978663 | snp | C/T | | | missense | LYST | GRCh38.p7 | 1:235709242 | AGACGAGGATCATTA[C/T]GCGCCCAAGGGGGAA | 1130 |
rs771987578 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810300 | GCTATGCCTTTTTCA[C/T]CTGAATTGGCTTCTG | 1130 |
rs772000938 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235715275 | GTGCCGCTATTGGAA[C/T]AGTGGGAGCCATAGT | 1130 |
rs772006444 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235676643 | CTTTCTGTTTCATAG[A/T]TGGAATGCTGCCTGA | 1130 |
rs772029414 | in-del | -/AAAAAAAAAAAAAAAAATAT | | | downstream-variant-500B | LYST | GRCh38.p7 | 1:235660716 | CTACTAAAAATACAA[-/AAAAAAAAAAAAAAAAATAT]AAAAAAAAAAAAAAA | 1130 |
rs772040832 | snp | A/G | | | intron-variant, synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747243 | TTGATTTAATGGACC[A/G]AAGGAGAAGGGCATC | 1130 |
rs772050829 | in-del | -/ATT | 6.59228e-05 | 0.00574083 | cds-indel, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804522 | CTCAGTCATAGCATC[-/ATT]ATGTTCAAAATCTGC | 1130 |
rs772060702 | snp | C/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235801055 | AAGTCATTTGGACTG[C/T]TTGATGCACTGAAAC | 1130 |
rs772065981 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235819732 | CTCACTGCAAGCTCT[G/T]CCTCCCAGGTTCACA | 1130 |
rs772066540 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698192 | TATTTTACTTTCAAC[G/T]CTTCAGAGGAAATGC | 1130 |
rs772081349 | in-del | -/T | | | intron-variant | LYST | GRCh38.p7 | 1:235856127 | TACCACACTGGGTAG[-/T]TTCTATCATACTCGG | 1130 |
rs772082423 | snp | A/G | 4.07864e-05 | 0.0045157 | intron-variant | LYST | GRCh38.p7 | 1:235793452 | ATTCTATTAAAAATT[A/G]TAAGTGAAAGAATTT | 1130 |
rs772083458 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235880080 | GTGAACTCTTGTCTC[G/T]TTTTTTCTTAGAGTT | 1130 |
rs772097841 | in-del | -/TGC | | | intron-variant | LYST | GRCh38.p7 | 1:235875564 | GGGGCAGCTACATCA[-/TGC]TGCTGATGGAAGGAG | 1130 |
rs772098917 | snp | A/T | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720848 | CGGTGATGTTACCAT[A/T]TTCCAGAAGATTAGG | 1130 |
rs772105553 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235772857 | CTGCCTGACTGCAGT[A/G]TTCTTAGCCAGCCCA | 1130 |
rs772144056 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235690450 | AACTTGTTTGTGTTT[C/G]GATATATATATTTCT | 1130 |
rs772148110 | in-del | -/G | | | intron-variant | LYST | GRCh38.p7 | 1:235717201 | TTTCGACAGAACTTA[-/G]GAACAGAGGAAGATG | 1130 |
rs772156213 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235698838 | AGATCACGCCACTGC[A/T]CTTCAGTCTGGGCAA | 1130 |
rs772173344 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235748043 | TGAGGGCTGAATAAA[C/T]GGATAAAGAAAGAGT | 1130 |
rs772178659 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809405 | CACACTATTTATTAG[A/G]GCTTTCAAATGCTCT | 1130 |
rs772179042 | snp | C/T | 1.6834e-05 | 0.00290116 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235813005 | GACAGGTATCTTCCA[C/T]ACCAGTGGAAGGAGA | 1130 |
rs772183331 | snp | A/G | 1.65806e-05 | 0.00287924 | synonymous-codon | LYST | GRCh38.p7 | 1:235664539 | GTTGGAGAAAGCCAC[A/G]GAACAGATGATCTCC | 1130 |
rs772185534 | in-del | -/A | 0.000330415 | 0.0128491 | intron-variant | LYST | GRCh38.p7 | 1:235747348 | TTGTTTTAAATTATG[-/A]AAAACATATATCAAT | 1130 |
rs772190526 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235837238 | CTGAGAAGGAACAGC[A/C]AGTGAGGCAGGAGAA | 1130 |
rs772199678 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, intron-variant | LYST | GRCh38.p7 | 1:235702812 | GCACTAGCAACCCCA[C/T]AGCAGCTGGAAGCTC | 1130 |
rs772221166 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235733441 | CGGAATACAAATTCC[A/G]TTTAACATCAATATC | 1130 |
rs772231809 | snp | A/C | | | intron-variant | LYST | GRCh38.p7 | 1:235686100 | GGCCGGGCGTGATGG[A/C]TCACACCTATAATCC | 1130 |
rs772245516 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235807689 | ACCAGTCTACCCATT[C/T]GTTTATAAAATTATT | 1130 |
rs772252784 | snp | A/T | 1.6549e-05 | 0.0028765 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235738603 | AGTGTGCCTGTATGG[A/T]GTAAAGCAAATGTTA | 1130 |
rs772255527 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235793450 | ACATTCTATTAAAAA[C/T]TGTAAGTGAAAGAAT | 1130 |
rs772263129 | snp | A/C | 0.000157913 | 0.00888434 | intron-variant | LYST | GRCh38.p7 | 1:235744180 | TTGAAAAAAAGAATA[A/C]AAAATTAGTCATATC | 1130 |
rs772285599 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235703304 | CAATATATAGGAAAA[A/G]GCAAAAATGAAGTTA | 1130 |
rs772285918 | in-del | -/AAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235872298 | GACATTCTGTCTCAA[-/AAAA]AAAAAAAAAAAAAAA | 1130 |
rs772286067 | in-del | -/GTAA | | | intron-variant, downstream-variant-500B | LYST, MIR1537 | GRCh38.p7 | 1:235852659 | TCAACTAATACTGAG[-/GTAA]GTGACAAGTTGATTG | 1130 |
rs772296728 | snp | C/T | 9.94431e-05 | 0.00705065 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235758990 | TGAGCACTTGCAGTT[C/T]GGTTGTAATTTGGCT | 1130 |
rs772304482 | snp | A/C | 1.65567e-05 | 0.00287716 | stop-gained, nc-transcript-variant | LYST | GRCh38.p7 | 1:235741484 | GTTCATGAACTATTT[A/C]AAAAATTTGCTTTCT | 1130 |
rs772305412 | snp | A/T | 3.30409e-05 | 0.0040644 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809564 | GGGATTTGAAGCTGC[A/T]CTTTGAAGACAACAG | 1130 |
rs772321055 | in-del | -/AAGAAAA | 3.32237e-05 | 0.00407563 | intron-variant | LYST | GRCh38.p7 | 1:235757495 | TCTTACTAACATGAC[-/AAGAAAA]GTACTTGATGATTAC | 1130 |
rs772323073 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235878738 | AATAGGAGAGCAAGG[A/G]TTTCCTGATGGGATA | 1130 |
rs772330561 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235705195 | GAGTGAGGATCTGAA[C/T]TCAATCCTTAATTCA | 1130 |
rs772344206 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853656 | CTCCCCAAGCCCATG[A/G]AATCTTGGTTAACAT | 1130 |
rs772351029 | snp | C/T | 1.65192e-05 | 0.00287391 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235753249 | TCTGAAACAATCCCA[C/T]GTTTCTCACATCTTC | 1130 |
rs772370931 | snp | A/G | 1.91265e-05 | 0.00309239 | intron-variant | LYST | GRCh38.p7 | 1:235759643 | TTAAAAATCTATTAA[A/G]TGGAACCACCTCTCT | 1130 |
rs772377288 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235673659 | CTTAGGTGCTTCTAT[G/T]GTCTAGGAGAAAATG | 1130 |
rs772379369 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235667295 | TTGGCAACAGAGGAC[C/G]AGGCTATGGATGTCT | 1130 |
rs772380539 | in-del | -/A | | | intron-variant | LYST | GRCh38.p7 | 1:235744940 | AAAGTAAAAAAAGCT[-/A]AAAAAAATAATAATA | 1130 |
rs772383764 | snp | C/T | 1.65853e-05 | 0.00287964 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235788839 | GCACCTTCTGGTCTG[C/T]CGCTCTCTATAAGAA | 1130 |
rs772393440 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235662407 | ATAAAATATTTGGTA[C/T]AGAGGCACCTACTGA | 1130 |
rs772399847 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235718218 | TTTGGACACAAGCTA[C/T]GTTAATAGTTGTAGC | 1130 |
rs772404333 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235780556 | TATGTCAAACTAACA[A/G]GTGTTATTTTCACTG | 1130 |
rs772429690 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235791932 | CTCTCTCTATCAGCC[C/T]CTTTCTTGCTCCGTG | 1130 |
rs772435657 | in-del | -/TGTGTGTGTGTGTGTGT | | | intron-variant | LYST | GRCh38.p7 | 1:235730596 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGT]GTATATGTAAACTAA | 1130 |
rs772450832 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235872167 | CAGGCATAGTGGCAC[A/G]TGCATGTAGTCTCAG | 1130 |
rs772463293 | in-del | -/C | | | intron-variant | LYST | GRCh38.p7 | 1:235684886 | TTCTTGTCTTGGCCT[-/C]CCAAAGTGCTGGGGC | 1130 |
rs772464242 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235761737 | CTGGATAGGGAAAGC[A/G]AGACAAGGGGAACTT | 1130 |
rs772464320 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743146 | TCTATGGGTTTACCA[C/T]AGAGTATTCCCTAAC | 1130 |
rs772468145 | snp | C/T | 1.92662e-05 | 0.00310366 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235780885 | AGAGACCAATATCCA[C/T]ATCTTTCTTGGTCAT | 1130 |
rs772476965 | snp | G/T | 1.69286e-05 | 0.0029093 | missense, nc-transcript-variant, intron-variant | LYST | GRCh38.p7 | 1:235752031 | TTGTTTTTGCTATTT[G/T]GAAGATATCCAAGCA | 1130 |
rs772520374 | snp | C/G | | | intron-variant | LYST | GRCh38.p7 | 1:235845240 | GCTGAAGGTCTGTTT[C/G]CTGGAGAAGTTTCTG | 1130 |
rs772536161 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235671714 | GTGAGGTTATAGCAT[A/G]GTGATTAAGAGAGAA | 1130 |
rs772543665 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235720704 | GTGTCTCACTAACGT[A/G]GTCAGCAAGTATAAA | 1130 |
rs772544391 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235701401 | TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGC | 1130 |
rs772545723 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant | LYST | GRCh38.p7 | 1:235733703 | GAGACTAAACAAATA[A/G]TAAGATTGTCCATAG | 1130 |
rs772546837 | snp | C/T | 4.95757e-05 | 0.00497849 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235806160 | TATCATAAATATTAA[C/T]TTATGGCATACTCGG | 1130 |
rs772552700 | snp | C/T | | | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661118 | GATAATTTACAGAAA[C/T]GTTTGCTACAACATG | 1130 |
rs772553841 | snp | A/T | | | intron-variant | LYST | GRCh38.p7 | 1:235743872 | TTTTAAAAAGCTCTC[A/T]GAAAGAGCACAAAGA | 1130 |
rs772554004 | snp | C/T | 6.84615e-05 | 0.0058503 | intron-variant | LYST | GRCh38.p7 | 1:235810569 | AGGCTTAGAATACCT[C/T]AATATGTTTTAAAAC | 1130 |
rs772560535 | snp | A/C/G | 9.96023e-05 | 0.00705636 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808843 | AGAGTTCAGCATCAC[A/C/G]TAAGTTTCCCTGCAG | 1130 |
rs772572715 | snp | C/T | 3.33228e-05 | 0.0040817 | intron-variant | LYST | GRCh38.p7 | 1:235746291 | TAGATTACTTCTCTT[C/T]CATTTTAAAATCTGA | 1130 |
rs772588112 | snp | G/T | 5.11849e-05 | 0.00505864 | intron-variant | LYST | GRCh38.p7 | 1:235800864 | TTTAACTAAATGAAT[G/T]TTTTACCTGTTGCAT | 1130 |
rs772592335 | in-del | -/CT | | | intron-variant | LYST | GRCh38.p7 | 1:235832170 | GAAAACATTTAAAAA[-/CT]CAACAGGTATAGTAC | 1130 |