SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11464 | snp | A/C | 0.0787734 | 0.182158 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235830265 | TGTCCATGGTCGAGG[A/C]TTTCTATTACTTACC | 1130 |
rs723716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYST | GRCh38.p7 | 1:235682408 | CTTCTCTGGGGCTTC[C/T]TCTCCATGTCCGCCA | 1130 |
rs767173 | snp | C/T | 0.132751 | 0.2208 | intron-variant | LYST | GRCh38.p7 | 1:235838361 | GAGTATTTGACAGTC[C/T]ACCATTCTATACTTG | 1130 |
rs941688 | snp | C/T | 0.115788 | 0.21092 | intron-variant | LYST | GRCh38.p7 | 1:235793902 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCATTG | 1130 |
rs957113 | snp | A/G | 0.463989 | 0.129263 | intron-variant | LYST | GRCh38.p7 | 1:235717416 | GAATGGTGTCATGTG[A/G]TGTTCACAGAATGTG | 1130 |
rs1063127 | snp | A/C/G | | | utr-variant-5-prime, nc-transcript-variant | LYST | GRCh38.p7 | 1:235883270 | AAGAGACCCAGTTTC[A/C/G]TTGCAGCTACCTGGG | 1130 |
rs1063128 | snp | A/G | 0.454992 | 0.143102 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809567 | GATCTGTTGTCTTCA[A/G]AGTGCAGCTTCAAAT | 1130 |
rs1063129 | snp | A/G | 0.00488995 | 0.0492043 | missense, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808713 | AGAACTTTGTTTTTG[A/G]AGAAGACAGATTACA | 1130 |
rs1063130 | snp | G/T | | | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235804582 | ACAACTAGCAAAGCC[G/T]TTATTTGATGCCCTG | 1130 |
rs1078858 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | LYST | GRCh38.p7 | 1:235748785 | TTTCTTCAGCAGTAC[C/T]GTCATTACATCTAGA | 1130 |
rs1078859 | snp | G/T | 0.465263 | 0.127129 | intron-variant | LYST | GRCh38.p7 | 1:235748725 | AGATACCATTTTATT[G/T]TCAGATTAATCTTAC | 1130 |
rs1111039 | snp | A/C | 0.463343 | 0.130326 | intron-variant | LYST | GRCh38.p7 | 1:235748292 | AAACTTTACACATCA[A/C]CCTTAATGCATGAAG | 1130 |
rs1858639 | snp | G/T | 0.48498 | 0.0853497 | intron-variant | LYST | GRCh38.p7 | 1:235760600 | GCCTGAGAATGTGAA[G/T]TCCCAACAATCCCAC | 1130 |
rs1858640 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | LYST | GRCh38.p7 | 1:235760182 | TTTACCTTGGACCAC[C/T]TCACTATCATTTGAA | 1130 |
rs1885252 | snp | C/T | 0.0988009 | 0.199095 | upstream-variant-2KB | LYST | GRCh38.p7 | 1:235885490 | AGATTCATATCATAA[C/T]ATCAGGTGGAGCCCA | 1130 |
rs2000305 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235709687 | ATGCTTCTACAAAGC[C/T]TTAGTTTGATTCTAA | 1130 |
rs2011390 | snp | C/T | 0.29789 | 0.24537 | intron-variant | LYST | GRCh38.p7 | 1:235782202 | AACAGAGCGAGACTC[C/T]GTCTCCAAAAAAAAA | 1130 |
rs2032032 | snp | C/T | 0.484632 | 0.086302 | intron-variant | LYST | GRCh38.p7 | 1:235807151 | GAGGGCAGGCAAGCA[C/T]GTGTTTGTTCATTAG | 1130 |
rs2032033 | snp | A/T | 0.484632 | 0.086302 | intron-variant | LYST | GRCh38.p7 | 1:235807257 | TAGAGCTGAAAATCT[A/T]CGGAAGGCTCAGCAT | 1130 |
rs2064903 | snp | A/G | 0.297128 | 0.245518 | intron-variant | LYST | GRCh38.p7 | 1:235829364 | TAAAATTTCTTTGCT[A/G]TGAAAGCATTTTGCT | 1130 |
rs2064904 | snp | C/G | 0.41507 | 0.187755 | intron-variant, nc-transcript-variant | LYST | GRCh38.p7 | 1:235827717 | CCTTCTTTCCACCTA[C/G]TCACTTTTTGGAATA | 1130 |
rs2104125 | snp | A/G | 0.288646 | 0.246995 | intron-variant | LYST | GRCh38.p7 | 1:235837005 | ATGAAATAACCCAGA[A/G]CAGTGCTGTTCACCG | 1130 |
rs2145401 | snp | C/T | 0.478685 | 0.10101 | intron-variant | LYST | GRCh38.p7 | 1:235829808 | TGAAAGCAGAGACCT[C/T]TTATGTGAACTAATA | 1130 |
rs2145402 | snp | G/T | 0.282375 | 0.248572 | intron-variant, downstream-variant-500B, nc-transcript-variant | LYST | GRCh38.p7 | 1:235738133 | AGAGCAAGTTCGCCT[G/T]CCAAGTCCTTCATTA | 1130 |
rs2145785 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | LYST | GRCh38.p7 | 1:235849832 | aaaggaattgaaaga[C/T]ctctacaaggaaaac | 1130 |
rs2145786 | snp | A/G | 0.266546 | 0.249452 | intron-variant | LYST | GRCh38.p7 | 1:235871998 | atttatttaatcaga[A/G]ttttacgtaacatgg | 1130 |
rs2180758 | snp | A/G | 0.236144 | 0.249616 | intron-variant | LYST | GRCh38.p7 | 1:235829974 | ACTATGCTTTTTATC[A/G]TAATATCAGTGAGAT | 1130 |
rs2180759 | snp | A/G | 0.298651 | 0.24522 | intron-variant | LYST | GRCh38.p7 | 1:235776503 | CAACAGTCTCACTTT[A/G]GTAAAAATCATTTCT | 1130 |
rs2208383 | snp | C/T | 0.316243 | 0.241064 | intron-variant | LYST | GRCh38.p7 | 1:235730615 | TTGTTAGTTTACATA[C/T]ACACACACACACACA | 1130 |
rs2208384 | snp | C/T | 0.296873 | 0.245566 | intron-variant | LYST | GRCh38.p7 | 1:235726796 | AAGAGTCTGAGTCCA[C/T]CTGTCGAATATGTTG | 1130 |
rs2273583 | snp | C/T | 0.00080004 | 0.0199845 | intron-variant | LYST | GRCh38.p7 | 1:235788873 | TACGAACCATTTTAC[C/T]GATCATTCTAACATC | 1130 |
rs2273584 | snp | A/G | 0.453984 | 0.144535 | synonymous-codon, nc-transcript-variant | LYST | GRCh38.p7 | 1:235777150 | ACCTCATCATCTAAA[A/G]AATCTCCAACCTACT | 1130 |
rs2273585 | snp | A/G | 0.423726 | 0.179776 | intron-variant | LYST | GRCh38.p7 | 1:235752840 | TTACTGAATGTCCCT[A/G]TATGCTACTTTATTA | 1130 |
rs2275856 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | LYST | GRCh38.p7 | 1:235709365 | TAAGACCTGCTCTGT[A/G]GCTGAATGAAACTTG | 1130 |
rs2385024 | snp | C/T | 0.443195 | 0.158668 | intron-variant | LYST | GRCh38.p7 | 1:235829344 | CCTCAATATATGTAT[C/T]TATTAGCAAAATGCT | 1130 |
rs2385025 | snp | C/T | 0.45235 | 0.146814 | intron-variant | LYST | GRCh38.p7 | 1:235836927 | GGAAGCTGGAACTAG[C/T]GAATCAATTTGGGAA | 1130 |
rs2385026 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYST | GRCh38.p7 | 1:235837698 | tgactgctggattta[A/G]caacatggaagttac | 1130 |
rs2385028 | snp | C/T | 0.264084 | 0.249603 | intron-variant | LYST | GRCh38.p7 | 1:235872505 | tgttccgattcttct[C/T]ggcatctgtgtgcag | 1130 |
rs2385029 | snp | A/G | 0.203575 | 0.245652 | intron-variant | LYST | GRCh38.p7 | 1:235881414 | TTAACATGCACAATC[A/G]GCTTTGAGGAAAAAT | 1130 |
rs2474929 | snp | A/G | 0.480853 | 0.0959518 | intron-variant | LYST | GRCh38.p7 | 1:235825266 | TAAGGAGAAGCATGA[A/G]GTATTTCACCATTAA | 1130 |
rs2489153 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | LYST | GRCh38.p7 | 1:235778232 | TGGGCCAGACACCAA[C/G]ATTCATGCCTATAAT | 1130 |
rs2489154 | snp | C/G | 0.28578 | 0.247426 | intron-variant | LYST | GRCh38.p7 | 1:235770754 | AAATTGCAGAATTTT[C/G]ACATTATCCATGACT | 1130 |
rs2489156 | snp | A/C | 0.297382 | 0.245469 | intron-variant | LYST | GRCh38.p7 | 1:235727231 | GGAGGCTGAGGCAGG[A/C]GAATCGCTTGAACCC | 1130 |
rs2753327 | snp | A/G | 0.00128518 | 0.0253167 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235731173 | TTTACTTGCAGAGCA[A/G]TATGGTATGACCCCA | 1130 |
rs2753328 | snp | A/G | 0.465263 | 0.127129 | intron-variant | LYST | GRCh38.p7 | 1:235764996 | AAAGAACTGCTGGTA[A/G]TATTACTAGTTGGAG | 1130 |
rs2753329 | snp | A/G | 0.48155 | 0.0942576 | intron-variant | LYST | GRCh38.p7 | 1:235743683 | TCATCATTGATGACT[A/G]CTATGGGAGTTTACA | 1130 |
rs2799440 | snp | G/T | | | intron-variant | LYST | GRCh38.p7 | 1:235785589 | atgttgcagaccttt[G/T]gctaggtgctttata | 1130 |
rs2799441 | snp | C/T | 0.48155 | 0.0942576 | intron-variant | LYST | GRCh38.p7 | 1:235749516 | ACAAAGGGGTGAGTA[C/T]AGGGGTGCATGTGCC | 1130 |
rs2799442 | snp | A/G | 0.275464 | 0.2487 | intron-variant | LYST | GRCh38.p7 | 1:235763837 | tcatctctcaactgg[A/G]ttactatcacagatt | 1130 |
rs2799443 | snp | A/G | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235797943 | GCTTATGTTTGAATT[A/G]GGTTGTTTCTTTTTT | 1130 |
rs2891663 | snp | C/T | 0.264084 | 0.249603 | intron-variant | LYST | GRCh38.p7 | 1:235870974 | CGATTTCAGCAATAG[C/T]AAGAAGGTCAGAATT | 1130 |
rs2891664 | snp | A/G | 0.077417 | 0.180873 | intron-variant | LYST | GRCh38.p7 | 1:235872275 | cactccagcccaggc[A/G]acggagtgacattct | 1130 |
rs2891665 | snp | C/T | 0.161924 | 0.233971 | intron-variant | LYST | GRCh38.p7 | 1:235873738 | CGGTCTACAAATTTC[C/T]GATTAACTTTCACCT | 1130 |
rs3047775 | snp | A/G | | | intron-variant | LYST | GRCh38.p7 | 1:235756063 | tctatatctatatct[A/G]tatctatatctatcC | 1130 |
rs3077214 | in-del | -/AAAA | | | intron-variant | LYST | GRCh38.p7 | 1:235872316 | AAAAAAAAAAAAAAA[-/AAAA]GTTTTATGTAACATG | 1130 |
rs3738519 | snp | C/T | 0.373946 | 0.217112 | intron-variant | LYST | GRCh38.p7 | 1:235758928 | AGAGTCTTTAAAGAA[C/T]AGTAAAATAAAGGTG | 1130 |
rs3738520 | snp | C/T | 0.45235 | 0.146814 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866598 | GCTCCCGCCCGCGGC[C/T]CGGCGGCTGTCAAAG | 1130 |
rs3738521 | snp | A/T | 0.46137 | 0.133501 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235866745 | TCAACCCAGGCTGAC[A/T]GCCACCAGCCCCAAA | 1130 |
rs3738522 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235866887 | ACTCCCCCTCTCCCG[A/G]AGAACCCCGAgccga | 1130 |
rs3754230 | snp | A/G | 0.239614 | 0.249784 | intron-variant | LYST | GRCh38.p7 | 1:235663283 | GATGCTCATAAATGC[A/G]GTGATATAGAATAAA | 1130 |
rs3754231 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235678599 | AAAAGTAGAAAGAAT[A/T]AGTATAATAAAGAGC | 1130 |
rs3754232 | snp | A/G | 0.372592 | 0.217879 | intron-variant | LYST | GRCh38.p7 | 1:235693601 | AACATATCATTTGGT[A/G]CAAGACCATCTTTAA | 1130 |
rs3754233 | snp | A/T | 0.48491 | 0.0855403 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235739200 | CTGTAGGTAGCTATA[A/T]CTTGTAGTACCATTC | 1130 |
rs3754234 | snp | C/T | 0.411234 | 0.191059 | intron-variant, missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235747242 | CTTGATTTAATGGAC[C/T]GAAGGAGAAGGGCAT | 1130 |
rs3754235 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235765419 | TTACTTATAGCCTTT[G/T]CTCAAAACAAACAAA | 1130 |
rs3768050 | snp | A/C | 0 | 0 | utr-variant-3-prime | LYST | GRCh38.p7 | 1:235661184 | GTTTCATGCTGAATA[A/C]ATAATCCCCCCaaat | 1130 |
rs3768051 | snp | G/T | 0.117886 | 0.21224 | intron-variant | LYST | GRCh38.p7 | 1:235696414 | GCATTTAACCTGATA[G/T]AAACAGATGAGTGCC | 1130 |
rs3768052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | LYST | GRCh38.p7 | 1:235713114 | CAACATCTTCTGTCA[C/T]TTGTATTACTTTCTC | 1130 |
rs3768054 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | LYST | GRCh38.p7 | 1:235728702 | TCTGAGGTTCCGCCC[C/T]CTGCATGCTCATCAC | 1130 |
rs3768056 | snp | A/G | 0.303438 | 0.244222 | intron-variant | LYST | GRCh38.p7 | 1:235744525 | GTGCTATACATTTAC[A/G]TGCTGTATATGTGAT | 1130 |
rs3768058 | snp | C/T | 0.48498 | 0.0853497 | intron-variant | LYST | GRCh38.p7 | 1:235761500 | TTAAAGACTTGAATA[C/T]ACTTACTATGGAAAT | 1130 |
rs3768059 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYST | GRCh38.p7 | 1:235771264 | GTAAACAAACAAATA[C/T]CAACAAAAAAAGAAA | 1130 |
rs3768060 | snp | A/C | 0.48378 | 0.0885831 | intron-variant | LYST | GRCh38.p7 | 1:235784595 | TGGCATGAGTTTGGG[A/C]AAGTCACTCTAGGTC | 1130 |
rs3768061 | snp | C/T | 0.133777 | 0.221342 | intron-variant | LYST | GRCh38.p7 | 1:235785980 | TATATTTCTAGCACT[C/T]TATCTGAATCTATCA | 1130 |
rs3768063 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LYST | GRCh38.p7 | 1:235807410 | TAATATAAGCCAGCT[A/G]GGTGATTCTCAGCCC | 1130 |
rs3768064 | snp | C/T | 0.165527 | 0.235296 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808339 | AAAGCCCTGGAGATA[C/T]CAGTGTTAGAAGTTT | 1130 |
rs3768065 | snp | A/G | 0.000753901 | 0.0194006 | intron-variant, upstream-variant-2KB | LYST | GRCh38.p7 | 1:235808434 | ACCCCCGCCCCCGCC[A/G]CCACCCACACACATA | 1130 |
rs3768066 | snp | A/G | 0.185576 | 0.241556 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235808463 | TACAAACCTGGATTT[A/G]AGCAGGATAGGCAGA | 1130 |
rs3768067 | snp | C/T | 0.00142099 | 0.0266172 | missense, nc-transcript-variant | LYST | GRCh38.p7 | 1:235810450 | GCACTTCCTTCTAAA[C/T]GTAATTTTTCCTGAG | 1130 |
rs3768068 | snp | C/G | 0.219049 | 0.248077 | intron-variant | LYST | GRCh38.p7 | 1:235831007 | ATTAAGGGAAATAAG[C/G]TACAGCAAACAGAAT | 1130 |
rs3768069 | snp | A/C | 0.45235 | 0.146814 | intron-variant | LYST | GRCh38.p7 | 1:235831555 | AGAGAAGTAGATAAA[A/C]ATGAAAGGGAAGTAC | 1130 |
rs3768070 | snp | C/G | 0.486266 | 0.0817214 | intron-variant | LYST | GRCh38.p7 | 1:235835221 | CGTGCCCAGCCCATA[C/G]AGATATTTTTAACTT | 1130 |
rs3768071 | snp | A/G | 0.450734 | 0.149016 | intron-variant | LYST | GRCh38.p7 | 1:235852417 | GTAGGATAGTACCAC[A/G]TAAGGCAAACAGTAA | 1130 |
rs3768072 | snp | C/T | 0.483126 | 0.0902898 | intron-variant, upstream-variant-2KB | LYST, MIR1537 | GRCh38.p7 | 1:235853415 | ATTTATTCTGTATTA[C/T]GCATTTAAGCTAAGT | 1130 |
rs3819013 | snp | A/G | 0.37138 | 0.218556 | intron-variant | LYST | GRCh38.p7 | 1:235664143 | TACATTTCCTTCCAC[A/G]TGATTTTTAACAAAT | 1130 |
rs3820553 | snp | C/T | 0.45495 | 0.143163 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LYST | GRCh38.p7 | 1:235809135 | CAAGGAAGCCTGCTG[C/T]AGTAAGCGCAAGCAC | 1130 |
rs3820554 | snp | C/T | | | intron-variant | LYST | GRCh38.p7 | 1:235831171 | AAAAGATATTTAACA[C/T]AGAGATGTTAAGTTA | 1130 |
rs3820555 | snp | A/G | 0.452227 | 0.146984 | intron-variant | LYST | GRCh38.p7 | 1:235831567 | AAAAATGAAAGGGAA[A/G]TACCAGAGAAATTCC | 1130 |
rs3820556 | snp | C/G | 0.105924 | 0.204309 | upstream-variant-2KB, intron-variant | LYST | GRCh38.p7 | 1:235866977 | CCGAGAACACCACCC[C/G]CTCCCTCCCCTCGTC | 1130 |
rs3831362 | in-del | -/GTT | | | intron-variant, downstream-variant-500B | LYST | GRCh38.p7 | 1:235715131 | GTTGTTGTTGTTGTT[-/GTT]TCTGATGACCCAACA | 1130 |
rs3835669 | in-del | -/C | 0.316243 | 0.241064 | intron-variant | LYST | GRCh38.p7 | 1:235749008 | AATCTATTTAGGAAT[-/C]CCCCCTACCACACCT | 1130 |
rs3841835 | in-del | -/TG | | | intron-variant | LYST | GRCh38.p7 | 1:235710363 | AACTCCATGTGTGTG[-/TG]GCTTCAGGAGCGGCA | 1130 |
rs3940062 | snp | A/C | 0 | 0 | intron-variant | LYST | GRCh38.p7 | 1:235748640 | CCAGTGAACAAAGCT[A/C]TGACTCCTTAACCTC | 1130 |
rs4006790 | in-del | -/TGTGTG | | | intron-variant | LYST | GRCh38.p7 | 1:235730606 | gtgtgtgtgtgtgtg[-/TGTGTG]tgtatatgtaAACTA | 1130 |
rs4233482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LYST | GRCh38.p7 | 1:235682038 | TTACGAAGATTTAAC[A/G]TGTGGCTCACGTCTG | 1130 |
rs4275443 | snp | A/C | 0.394904 | 0.203722 | intron-variant | LYST | GRCh38.p7 | 1:235685859 | TTAAAACAAAACAAA[A/C]AAAAAAAAACAAACA | 1130 |
rs4306114 | snp | A/T | 0.422787 | 0.180679 | intron-variant | LYST | GRCh38.p7 | 1:235754385 | TTACATGAATGTGCC[A/T]CCACGCCCAGCAAAT | 1130 |
rs4319315 | snp | C/T | 0.396182 | 0.202807 | intron-variant | LYST | GRCh38.p7 | 1:235689047 | caacaacaacaacaa[C/T]aataatatcctagct | 1130 |
rs4366309 | snp | A/G | 0.482979 | 0.0906686 | intron-variant | LYST | GRCh38.p7 | 1:235848386 | tggagcaagggtggt[A/G]ctaagaggaaagttc | 1130 |
rs4373748 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | LYST | GRCh38.p7 | 1:235688766 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 1130 |