SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs729496 | snp | C/G | 0.499878 | 0.00781361 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974350 | TTCTCTTGGGCTTCT[C/G]AGTCTCCAAACCCCA | 79836 |
rs907798 | snp | A/G | 0.0333324 | 0.12472 | intron-variant | LONRF3 | GRCh38.p7 | X:118983843 | AGAAAGGAATAGTTA[A/G]CAAAATCAATGAAAT | 79836 |
rs1031565 | snp | C/T | 0.132815 | 0.220834 | intron-variant | LONRF3 | GRCh38.p7 | X:118978031 | TACACACGGCTAGTG[C/T]CCGGCAGCCTGGTTT | 79836 |
rs1398869 | snp | A/G | 0.113499 | 0.209446 | intron-variant | LONRF3 | GRCh38.p7 | X:118977378 | CCACATTCCCCTGGA[A/G]GTTCTTCCTTGCATC | 79836 |
rs1455862 | snp | A/G | 0.435961 | 0.167089 | intron-variant | LONRF3 | GRCh38.p7 | X:119001960 | ATATTATTTGATGGT[A/G]CTAATGATGAAGATG | 79836 |
rs1807937 | snp | C/T | 0.482857 | 0.0909818 | intron-variant | LONRF3 | GRCh38.p7 | X:118996217 | ctttcaacttttccc[C/T]gttcagtattatgAC | 79836 |
rs1975779 | snp | A/G/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118979282 | Agcgcggtggctcac[A/G/T]cctgtaatcccagca | 79836 |
rs2100524 | snp | A/T | 0.497754 | 0.0334346 | intron-variant | LONRF3 | GRCh38.p7 | X:118993193 | acctcttcaattctt[A/T]ttcaggtaaatcaag | 79836 |
rs2100525 | snp | A/G | 0.48927 | 0.0724549 | intron-variant | LONRF3 | GRCh38.p7 | X:118992810 | tgggtctctcagtag[A/G]tagataccagtgcct | 79836 |
rs2100526 | snp | C/T | 0.497754 | 0.0334346 | intron-variant | LONRF3 | GRCh38.p7 | X:118992778 | ttctggtggaggtgg[C/T]ggtgggtgcaatgga | 79836 |
rs2100527 | snp | A/T | 0.49779 | 0.0331715 | intron-variant | LONRF3 | GRCh38.p7 | X:118992775 | tggtggaggtggtgg[A/T]gggtgcaatggactc | 79836 |
rs2124399 | snp | C/T | 0.477825 | 0.102937 | intron-variant | LONRF3 | GRCh38.p7 | X:119015403 | ACTGGTGTCTTAGAA[C/T]CTCAGAATGCAAGAG | 79836 |
rs2124400 | snp | C/T | 0.486987 | 0.0796057 | intron-variant | LONRF3 | GRCh38.p7 | X:119015306 | CTTCCCAAGGTCATA[C/T]TGCTAGTGAGGTAAG | 79836 |
rs2124401 | snp | A/G | 0.478269 | 0.101948 | intron-variant | LONRF3 | GRCh38.p7 | X:119015235 | TTTCTTTTGTGACAG[A/G]GTTGGGGATGAGCAT | 79836 |
rs2168377 | snp | G/T | 0.0369084 | 0.130736 | intron-variant | LONRF3 | GRCh38.p7 | X:119015476 | TGCCTTTGCATGGGG[G/T]GGGAAAGAAGCCACC | 79836 |
rs2168378 | snp | C/G | 0.30475 | 0.243931 | intron-variant | LONRF3 | GRCh38.p7 | X:119015168 | ATAGGAAGAGATGGT[C/G]GTGAGGAAATATGTG | 79836 |
rs2168379 | snp | C/T | 0.471939 | 0.115078 | intron-variant | LONRF3 | GRCh38.p7 | X:119009080 | CAATTAGGTAATACG[C/T]AGCAATCAGCAAAAC | 79836 |
rs2278954 | snp | C/T | 0.473172 | 0.11267 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014266 | ATGAAACCACAATGA[C/T]GCTTGCTGATAGACA | 79836 |
rs2290514 | snp | A/C | 0.486294 | 0.081639 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013270 | TGAGAAATCCTTTCA[A/C]AACTATCTTTGTGTA | 79836 |
rs2316007 | snp | G/T | 0.0414859 | 0.13792 | intron-variant | LONRF3 | GRCh38.p7 | X:119016695 | TCACAACCTCACTTT[G/T]CAAAAATTCCAATTA | 79836 |
rs2316008 | snp | A/G | 0.447004 | 0.153913 | intron-variant | LONRF3 | GRCh38.p7 | X:119010208 | GAGAGCCTCAATGAC[A/G]CCTCTGCCCCTCCCC | 79836 |
rs2316009 | snp | C/T | 0.0348667 | 0.127349 | intron-variant | LONRF3 | GRCh38.p7 | X:119010168 | CACATTACCTGTGCA[C/T]GGCAGAGAAAGCGCT | 79836 |
rs2316010 | snp | G/T | 0.0414859 | 0.13792 | intron-variant | LONRF3 | GRCh38.p7 | X:118995805 | ttattggtctgttca[G/T]ggtatctcatccttc | 79836 |
rs3049095 | in-del | -/GTCT | 0.0235569 | 0.105941 | intron-variant | LONRF3 | GRCh38.p7 | X:118977089 | TGTTTAGTCTTTTCT[-/GTCT]TTTTTCTTCTGCAGC | 79836 |
rs3747384 | snp | C/G | 0.32817 | 0.237465 | intron-variant | LONRF3 | GRCh38.p7 | X:118990277 | AGAGGTTTCCAGCAG[C/G]CCCAACAGAAAGAGA | 79836 |
rs3813933 | snp | A/G | 0.496518 | 0.0415792 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974822 | GTCGCTGCTGACCTC[A/G]GCGGGCAAGCTCAGC | 79836 |
rs3813935 | snp | A/C | 0.166434 | 0.23562 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974127 | CCGTGAAGCCCCCCC[A/C]CACACACACAACCCA | 79836 |
rs3827453 | snp | C/G | 0.455119 | 0.14292 | intron-variant | LONRF3 | GRCh38.p7 | X:118990731 | CAGGGAATGCAGTCT[C/G]TGGGAAGGGGACACA | 79836 |
rs4581223 | snp | A/C | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118997398 | tttcaacaaatggtg[A/C]tgggataattggcta | 79836 |
rs4825394 | snp | A/T | 0.498408 | 0.028167 | intron-variant | LONRF3 | GRCh38.p7 | X:118994056 | aatcctggaaacaca[A/T]caaaacagaacctct | 79836 |
rs4825623 | snp | C/T | 0.305742 | 0.243707 | intron-variant | LONRF3 | GRCh38.p7 | X:118988331 | TGAAAAGAAGAAAAA[C/T]AGCAACCTTGGCTTT | 79836 |
rs4825625 | snp | C/T | 0.389954 | 0.207154 | intron-variant | LONRF3 | GRCh38.p7 | X:119009855 | GCTTACTGCAACCTC[C/T]GCCTTCCGGGTTCAA | 79836 |
rs5903535 | in-del | -/C | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974492 | CGAAGCCCAAAGAAG[-/C]CAAGAGCAACACTGT | 79836 |
rs5909579 | snp | A/G | 0.300422 | 0.244862 | intron-variant | LONRF3 | GRCh38.p7 | X:118980632 | GTTTTTTTTCCCCAA[A/G]GAACACATTTAGTGT | 79836 |
rs5909580 | snp | C/T | 0.323794 | 0.238861 | intron-variant | LONRF3 | GRCh38.p7 | X:118984714 | GATGATGCAAGCGAG[C/T]GTATGCCCGTGATGA | 79836 |
rs5909581 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | LONRF3 | GRCh38.p7 | X:118987829 | CTGCACTATGCCTTA[C/T]ACATAAGTAAGCTTC | 79836 |
rs5909583 | snp | A/G | 0.499113 | 0.0210409 | intron-variant | LONRF3 | GRCh38.p7 | X:119002451 | ttattgcatataggt[A/G]aagtttgttcacttt | 79836 |
rs5910465 | snp | A/G | 0.465403 | 0.126891 | intron-variant | LONRF3 | GRCh38.p7 | X:118978896 | ctaataatgtaaggt[A/G]cttagaacagtgtct | 79836 |
rs5910466 | snp | C/T | 0.438029 | 0.164757 | intron-variant | LONRF3 | GRCh38.p7 | X:118978897 | TAATAATGTAAGGTA[C/T]TTAGAACAGTGTCTG | 79836 |
rs5910467 | snp | A/G | 0.377438 | 0.21508 | intron-variant | LONRF3 | GRCh38.p7 | X:118980222 | CCTTATCTGAATCTT[A/G]TAAGACCAGAGGTGT | 79836 |
rs5910468 | snp | A/T | 0.389207 | 0.207657 | intron-variant | LONRF3 | GRCh38.p7 | X:118980356 | AAAATTCACACTCAG[A/T]GGGACAAATATTTTT | 79836 |
rs5910469 | snp | C/T | 0.462705 | 0.131365 | intron-variant | LONRF3 | GRCh38.p7 | X:118983627 | TCATGGACTTTGTTG[C/T]TTATTGTTCTACAGT | 79836 |
rs5910470 | snp | C/T | 0.463996 | 0.129251 | intron-variant | LONRF3 | GRCh38.p7 | X:118984722 | AAGCGAGTGTATGCC[C/T]GTGATGAGTGTTACA | 79836 |
rs5910471 | snp | A/G | 0.240609 | 0.249824 | intron-variant | LONRF3 | GRCh38.p7 | X:118986529 | TTCTCTCCTGACTTT[A/G]CCTCTCTGTCTCTTT | 79836 |
rs5910473 | snp | G/T | 0.462849 | 0.13113 | intron-variant | LONRF3 | GRCh38.p7 | X:118989802 | CTCTGGCATTTACTA[G/T]CTGTGTGACCTCAGA | 79836 |
rs5910474 | snp | A/C | 0.495428 | 0.0475954 | intron-variant | LONRF3 | GRCh38.p7 | X:118991255 | CGCCCCCGCCACCCA[A/C]CTGCCTTATTCCAAC | 79836 |
rs5910479 | snp | C/T | 0.017851 | 0.0927731 | intron-variant | LONRF3 | GRCh38.p7 | X:119000566 | TGTGGTTACCTTAGC[C/T]ATTGGGGGCCACCTC | 79836 |
rs5910480 | snp | A/C | 0.435581 | 0.16751 | intron-variant | LONRF3 | GRCh38.p7 | X:119003500 | gtattgaaaatcttt[A/C]ccccatctgctttga | 79836 |
rs5910481 | snp | C/T | 0.497847 | 0.0327373 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012847 | atggtagCAGTTACA[C/T]GAATACATTACGAAT | 79836 |
rs5956093 | snp | A/G | 0.438029 | 0.164757 | intron-variant | LONRF3 | GRCh38.p7 | X:118981374 | CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGG | 79836 |
rs5956094 | snp | C/T | 0.325989 | 0.238171 | intron-variant | LONRF3 | GRCh38.p7 | X:118981416 | CTTGAACCTAGGAGG[C/T]GGAGGTTGTAGTGAG | 79836 |
rs5956095 | snp | C/T | 0.489115 | 0.0729673 | intron-variant | LONRF3 | GRCh38.p7 | X:118988557 | GTTTTCTCCCAGCTA[C/T]ATGCTCCCCTTTTTC | 79836 |
rs5956096 | snp | C/T | 0.0965482 | 0.197364 | intron-variant | LONRF3 | GRCh38.p7 | X:118996660 | aggtgcggtggctca[C/T]gcctgtaatcccagc | 79836 |
rs5956098 | snp | A/C | 0.30475 | 0.243931 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013655 | ATAATCCATCATCCC[A/C]TAAGGCAGAAAGATG | 79836 |
rs5957086 | snp | G/T | 0.389207 | 0.207657 | intron-variant | LONRF3 | GRCh38.p7 | X:118981365 | TGACGCATGCCTGTA[G/T]TCCCAGCTACTCAGG | 79836 |
rs5957087 | snp | A/T | 0.46256 | 0.131599 | intron-variant | LONRF3 | GRCh38.p7 | X:118987419 | AGTAGCTGGGACTAT[A/T]GGCACGTGCCACCAT | 79836 |
rs5957088 | snp | C/T | 0.482561 | 0.0917346 | intron-variant | LONRF3 | GRCh38.p7 | X:118987424 | CTGGGACTATAGGCA[C/T]GTGCCACCATGCCTG | 79836 |
rs5957090 | snp | A/G | 0.483919 | 0.0882151 | intron-variant | LONRF3 | GRCh38.p7 | X:118997865 | atggccaacaaacat[A/G]aagaaatgctcagca | 79836 |
rs5957091 | snp | A/G | 0.0733812 | 0.176934 | intron-variant | LONRF3 | GRCh38.p7 | X:118998940 | gctgggattacaggc[A/G]tgagccactatgcct | 79836 |
rs5957093 | snp | C/T | 0.426333 | 0.177219 | intron-variant | LONRF3 | GRCh38.p7 | X:119006883 | gtgagccaccacgcc[C/T]ggcctaatttttgta | 79836 |
rs5957094 | snp | A/C | 0.453518 | 0.145191 | intron-variant | LONRF3 | GRCh38.p7 | X:119016504 | AGAAGCCCGCCACCG[A/C]GCCCGGCTAATTTTT | 79836 |
rs5957095 | snp | A/G | 0.30475 | 0.243931 | intron-variant | LONRF3 | GRCh38.p7 | X:119016704 | TTTTTGCAAAGTGAG[A/G]TTGTGATTCTTTGGG | 79836 |
rs6603457 | snp | C/T | 0.482561 | 0.0917346 | intron-variant | LONRF3 | GRCh38.p7 | X:118986681 | TTCCTGGGCCACACT[C/T]CAGACCTGGGGGAGA | 79836 |
rs6603465 | snp | A/G | 0.496821 | 0.0397406 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013502 | AAGATTGCAAGGAAT[A/G]GATCTGGGGTGGGTC | 79836 |
rs6645535 | snp | G/T | 0.0806904 | 0.183941 | intron-variant | LONRF3 | GRCh38.p7 | X:119000971 | ACAAGGATGTAACTG[G/T]TGGGAAAAGATAGCT | 79836 |
rs6645536 | snp | A/G | 0.0738704 | 0.177421 | intron-variant | LONRF3 | GRCh38.p7 | X:119009863 | CAACCTCCGCCTTCC[A/G]GGTTCAAGCGATTCT | 79836 |
rs6646305 | snp | C/T | 0.0845627 | 0.187431 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976595 | CCCGCTTTTCAGTGC[C/T]GCCTGGGAGGGTTGG | 79836 |
rs6646306 | snp | C/T | 0.0903376 | 0.192374 | intron-variant | LONRF3 | GRCh38.p7 | X:118979069 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 79836 |
rs6646308 | snp | C/T | 0.0797195 | 0.183042 | intron-variant | LONRF3 | GRCh38.p7 | X:118980125 | CAAGCTATAAAGCTT[C/T]CTGGATGTAGTGCTC | 79836 |
rs6646309 | snp | A/G | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118980584 | CATTTTTTTTTCTGA[A/G]AAGGTTTTCTTGAGT | 79836 |
rs6646314 | snp | A/G | 0.0738704 | 0.177421 | intron-variant | LONRF3 | GRCh38.p7 | X:119010197 | TGAGAGGTGAAGGGG[A/G]GGGGCAGAGGCGTCA | 79836 |
rs6646315 | snp | C/T | 0.0669955 | 0.170321 | intron-variant | LONRF3 | GRCh38.p7 | X:119016095 | AGTGAGATTTGGTGA[C/T]GATCAGAGGAACCAA | 79836 |
rs7053662 | snp | G/T | 0.089378 | 0.191574 | intron-variant | LONRF3 | GRCh38.p7 | X:119005060 | AGCTGGCATGTTGCT[G/T]CTTCTACTCAGTCTG | 79836 |
rs7054507 | snp | G/T | 0.0845627 | 0.187431 | intron-variant | LONRF3 | GRCh38.p7 | X:118983928 | TGCTTTGAATTGGTT[G/T]GAGTATGTGAAAAAG | 79836 |
rs7054825 | snp | A/C | 0.00787002 | 0.062234 | intron-variant | LONRF3 | GRCh38.p7 | X:118993129 | tctaacacccccccc[A/C]aaaaaccacactagt | 79836 |
rs7063603 | snp | A/G | 0.0430067 | 0.140192 | intron-variant | LONRF3 | GRCh38.p7 | X:118979211 | gttttcaccgtgtta[A/G]ccaggatggtctcga | 79836 |
rs7064296 | snp | A/G | 0.0826288 | 0.185706 | intron-variant | LONRF3 | GRCh38.p7 | X:118988164 | CTGAAATGCAGGTGC[A/G]CCCAACTTTTCTTAA | 79836 |
rs7066489 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119016501 | tacagaagcccgcca[A/C]cgcgcccggctaatt | 79836 |
rs7067172 | snp | C/G | 0.0440191 | 0.141675 | intron-variant | LONRF3 | GRCh38.p7 | X:118984069 | ttgagaatttcttct[C/G]cattatacactgtgc | 79836 |
rs7879672 | snp | A/G | 0.018891 | 0.0953342 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017904 | GCTTCTTGACATGCT[A/G]CATAACTACATAAAC | 79836 |
rs7882263 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:118993562 | aataataatcggtgt[A/G]cctgtggaagaagaa | 79836 |
rs7883690 | snp | C/T | 0.496693 | 0.0405276 | intron-variant | LONRF3 | GRCh38.p7 | X:119016053 | AGAATGCAAATGAAG[C/T]TAGAGGCACAAAGAA | 79836 |
rs9792799 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981634 | CCTTGGTAAACACTG[A/C]TGGGAGAAGCAACAA | 79836 |
rs10127384 | snp | A/G | 0.0748481 | 0.178387 | intron-variant | LONRF3 | GRCh38.p7 | X:119006562 | catgccaccacgctc[A/G]gctaatttttgtttt | 79836 |
rs10465423 | snp | A/G | 0.462849 | 0.13113 | intron-variant | LONRF3 | GRCh38.p7 | X:118989127 | GCATTTCCCCTTTTT[A/G]CACCTGCCCAAGGAG | 79836 |
rs10587850 | in-del | -/TTGTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006601 | TTGTTTTGTTTTGTT[-/TTGTT]GAGACGGAGTCTCGC | 79836 |
rs10640705 | in-del | -/T/TC/TT/TTCC/TTTCT/TTTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016366 | TTTTTTTTTTTTTTT[-/T/TC/TT/TTCC/TTTCT/TTTT]GAGACGGAGTCTTGC | 79836 |
rs10669908 | in-del | -/AAA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981499 | AAAAAAAAAAAAAAA[-/AAA]GAGTATATGGATTGC | 79836 |
rs11377517 | in-del | -/A/AA | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019161 | AAAAAAAAAAAAAAA[-/A/AA]GGGAACCAGATAATC | 79836 |
rs11406051 | in-del | -/T | 0.498408 | 0.028167 | intron-variant | LONRF3 | GRCh38.p7 | X:118991393 | TGTCACCACCACAGA[-/T]CTATTCTTGGGAAGC | 79836 |
rs12156701 | snp | A/C | | | synonymous-codon, nc-transcript-variant, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013054 | GTTTGCAGAATATGG[A/C]TGCATCCTAGAGATC | 79836 |
rs12391696 | snp | C/T | 0.390203 | 0.206986 | intron-variant | LONRF3 | GRCh38.p7 | X:118983100 | AGATGGGAGTGTTAA[C/T]TGATTGCCCAGAAAC | 79836 |
rs12556024 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118996399 | tgctgatgatatgat[C/T]gtttaccttgaaaac | 79836 |
rs12558411 | snp | C/T | 0.436528 | 0.166455 | intron-variant | LONRF3 | GRCh38.p7 | X:119003856 | tccaatagaggtctc[C/T]tacaactgttgttag | 79836 |
rs12687273 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007983 | TTTAGTATCAGCAGA[A/G]GAGTCACCTACTTTT | 79836 |
rs12832094 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014599 | GCAGGTTTTGAGAAC[A/T]AAGTAAGATAAGAGA | 79836 |
rs12838954 | snp | A/G | 0.0348667 | 0.127349 | intron-variant | LONRF3 | GRCh38.p7 | X:119004233 | TATTAGTTTTAATTA[A/G]TTTGTTAAACAAATT | 79836 |
rs12843423 | snp | C/G/T | 0.0772873 | 0.180749 | intron-variant | LONRF3 | GRCh38.p7 | X:118990967 | agttcaagcgattca[C/G/T]gtgcctcagcctctt | 79836 |
rs12844427 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978857 | agcagctactaaaga[A/G]ggctgttgtgaggat | 79836 |
rs12844457 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978901 | aatgtaaggtactta[A/G]aacagtgtctggcat | 79836 |
rs12848578 | snp | A/G | 0.0343555 | 0.126481 | intron-variant | LONRF3 | GRCh38.p7 | X:118983090 | GACAAAAGGGAGATG[A/G]GAGTGTTAATTGATT | 79836 |
rs12851822 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014583 | GGAACTTGGATCCAA[G/T]GCAGGTTTTGAGAAC | 79836 |
rs12851824 | snp | G/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:119014584 | GAACTTGGATCCAAG[G/T]CAGGTTTTGAGAACT | 79836 |
rs12851827 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014593 | TCCAAGGCAGGTTTT[A/G]AGAACTAAGTAAGAT | 79836 |
rs12853640 | snp | A/G | 0.0763124 | 0.179813 | intron-variant | LONRF3 | GRCh38.p7 | X:118996105 | tgttaatcataaagc[A/G]atgctggattttgtt | 79836 |
rs12854678 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014520 | AGCGTCATGAGTAAG[A/C]CCAAAAAGATCCCAA | 79836 |
rs12859422 | snp | A/G | 0.0353775 | 0.128208 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012050 | GGGGTACTCCCAGGA[A/G]ACAGGGAGGCCTAGC | 79836 |
rs13441179 | snp | G/T | 0.0748481 | 0.178387 | intron-variant | LONRF3 | GRCh38.p7 | X:119011457 | ACACCTGAAAAGATT[G/T]TTTTGAGTGGAGAGC | 79836 |
rs13441224 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006908 | tttgtatttttagta[A/G]aaatggggtttcacc | 79836 |
rs16995350 | snp | A/G | 0.0417259 | 0.138282 | intron-variant | LONRF3 | GRCh38.p7 | X:118982773 | TGTTAGAGCAGTAGT[A/G]TTAATAGGCTGAATA | 79836 |
rs16995372 | snp | C/T | 0.0748481 | 0.178387 | intron-variant | LONRF3 | GRCh38.p7 | X:119014659 | ACCTTCCATGGGAGT[C/T]CAGATTCACACCATG | 79836 |
rs17261040 | snp | C/T | 0.0607552 | 0.16336 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012013 | AGGGAGGTTGTGTAA[C/T]GAGGGATTTCTGTTT | 79836 |
rs28412034 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999449 | TGTGGCTCTAAGCCC[A/C]TGATGTGCGCTGTGG | 79836 |
rs33971785 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991394 | GTCACCACCACAGAC[-/T]TATTCTTGGGAAGCC | 79836 |
rs34083222 | in-del | -/T/TT | 0.0022892 | 0.0337544 | intron-variant | LONRF3 | GRCh38.p7 | X:118994409 | ATCAGACAAAACAAA[-/T/TT]TTTTTTTTTTTTTGA | 79836 |
rs34187529 | in-del | -/A | 0.20797 | 0.246442 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018280 | GTTTACCATGTACCT[-/A]GGGGGAAATAACAAT | 79836 |
rs34378808 | in-del | -/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984316 | AGGACATGGCCACAG[-/C]CCTTAGCACTCACTG | 79836 |
rs34587594 | snp | A/G | 0.0235569 | 0.105941 | intron-variant | LONRF3 | GRCh38.p7 | X:118980230 | GAATCTTATAAGACC[A/G]GAGGTGTTCAGAATC | 79836 |
rs34597845 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975990 | TTCCTCTGACTCTCC[-/TTC]TCCCGCTGCACTCCT | 79836 |
rs34683146 | snp | C/G | 0.0768 | 0.180282 | intron-variant | LONRF3 | GRCh38.p7 | X:119000478 | TGAGAGAAGTTACCC[C/G]CTAACTTCAACCCTT | 79836 |
rs34741214 | in-del | -/T/TT | 0 | 0 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972975 | TCTCCTTCTTCTTCA[-/T/TT]TTTTTTTTTTTTTTC | 79836 |
rs34744749 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983938 | TGGTTTGAGTATGTG[-/A]AAAAGGTGTGCTTGA | 79836 |
rs34854698 | snp | A/G | 0.017851 | 0.0927731 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976602 | TTCAGTGCCGCCTGG[A/G]AGGGTTGGGTGGGCT | 79836 |
rs34889238 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987283 | TTATTCATTACATTG[-/A]AAAAAAAATTATGAA | 79836 |
rs34924772 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981322 | AACCCCATCTCTACT[-/A]AAAAATACAAAACTT | 79836 |
rs34988532 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976165 | TTGCCCCTTCCGGGG[-/C]CGCGGCTCCCTGTGG | 79836 |
rs35249118 | in-del | -/A | 0.355556 | 0.226623 | intron-variant | LONRF3 | GRCh38.p7 | X:118977170 | TGGGGAAAAAAAAAA[-/A]CATCAAAGCCTGTTG | 79836 |
rs35344521 | in-del | -/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008318 | GGCGCTCCCCCTGCT[-/G]GGGACTGTAGGGGTA | 79836 |
rs35356301 | in-del | -/CACA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986053 | TTCAGTATATGGAAA[-/CACA]CACACACACACACAC | 79836 |
rs35403613 | in-del | -/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999218 | AACAGCTCAGCAGGT[-/G]GGAATGTTGAAGCAC | 79836 |
rs35420687 | in-del | -/CA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118996035 | CAGGAAAGGACAACC[-/CA]AAAAAAAGAAAACCA | 79836 |
rs35489037 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981279 | ACTTGAGGTTAGGAG[-/T]TTTGAGACCAGCCTG | 79836 |
rs35967282 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018391 | ATGGATGCTTAAAAG[-/A]AAGTTCAGAATGATG | 79836 |
rs36016675 | in-del | -/T | 0.436905 | 0.166031 | intron-variant | LONRF3 | GRCh38.p7 | X:118979018 | TTTCTGTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 79836 |
rs36019440 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010609 | TAAGGTCTTATTAAC[-/A]AAATACTGAGATGTA | 79836 |
rs36037068 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118996216 | GTCATAATACTGAAC[-/A]GGGGAAAAGTTGAAA | 79836 |
rs36091758 | snp | A/T | 0.0078152 | 0.0620204 | intron-variant | LONRF3 | GRCh38.p7 | X:118978511 | TGTACTGTAGACAGG[A/T]ATTGGCAGGAAGGGC | 79836 |
rs36113925 | snp | C/T | 0.0343555 | 0.126481 | intron-variant | LONRF3 | GRCh38.p7 | X:118980903 | GATGAAAGTATTAAA[C/T]AGGAGTTTCATTTCC | 79836 |
rs41300317 | snp | C/T | 0.0328263 | 0.123837 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978373 | CTTGCTTTATAGCAA[C/T]CGGTCTCAGATTTAT | 79836 |
rs41304512 | snp | C/T | 0.0131573 | 0.0800346 | intron-variant | LONRF3 | GRCh38.p7 | X:118982743 | ACACAACAGTGAGTG[C/T]TGTGGGTTAGTTATT | 79836 |
rs41309532 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | LONRF3 | GRCh38.p7 | X:119009457 | GTTAAACATACCAGC[A/G]TACCACTGAAGAAGC | 79836 |
rs45519333 | snp | C/G | 0.0147244 | 0.0845304 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976531 | GCGCGGCAACTGCTT[C/G]GGGATCCCTGGGGAC | 79836 |
rs55763601 | snp | A/G | 0.254907 | 0.249952 | intron-variant | LONRF3 | GRCh38.p7 | X:118979487 | TTTAGTAGTGACGGG[A/G]TTTTGCCATGTTGGC | 79836 |
rs56862820 | in-del | -/ATGTT/TTGTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006605 | TTGTTTTGTTTTGTT[-/ATGTT/TTGTT]GAGACGGAGTCTCGC | 79836 |
rs57579693 | in-del | -/A | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972615 | AAAAAAAAAAAAAAA[-/A]TCTAGCTCAGGTCTG | 79836 |
rs57792543 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987868 | ATTTGTAACAGAGAA[A/G]AGGAAAGAGATGTTG | 79836 |
rs58137872 | in-del | -/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118991865 | TAACTATTTTTTTTT[-/T]CCTTGTAGACCAGAG | 79836 |
rs58462205 | snp | C/T | 0.273103 | 0.24893 | intron-variant | LONRF3 | GRCh38.p7 | X:118977273 | GAGGTCACTTAACTC[C/T]AGATCTCTAAGGCAG | 79836 |
rs58488155 | snp | A/T | 0.0142023 | 0.083063 | intron-variant | LONRF3 | GRCh38.p7 | X:118997785 | CAAATCAGTAAGAAA[A/T]AAACAATCCCATCAA | 79836 |
rs58491313 | in-del | -/T/TTTTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987446 | TTTTTTTTTTTTTTT[-/T/TTTTT]GTAGAGACGGGGTTT | 79836 |
rs58513403 | in-del | -/T/TT | 0.348482 | 0.240338 | intron-variant | LONRF3 | GRCh38.p7 | X:118980570 | GTGATGATGGATTCA[-/T/TT]TTTTTTTTTCTGAGA | 79836 |
rs58609623 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118996938 | AAAAAAAAAAAAAAA[-/A]GCAAAGAAAAGAAAA | 79836 |
rs59064728 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992680 | CACAGCTGTTGTTTT[A/C]TGGAAAGCACCACCT | 79836 |
rs59338453 | snp | A/G | 0.0358881 | 0.129059 | intron-variant | LONRF3 | GRCh38.p7 | X:118978121 | GAACCACTTGTGAGC[A/G]GGGGCAAAAATGACT | 79836 |
rs59344711 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118995425 | TCTAAGGTCACACCT[C/T]AAGGAACTAGAGAAA | 79836 |
rs59539866 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004140 | TTTTTTCTTGCCTTA[A/G]TGCACTGAGACCTCC | 79836 |
rs59700507 | in-del | -/GTGT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003987 | TGTGTGCACGTGTGT[-/GTGT]ATTTATCTAGTAACT | 79836 |
rs60364578 | in-del | -/CACACACACA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986093 | ACACACACACACACA[-/CACACACACA]ATCCTTGCTAGTACA | 79836 |
rs60614453 | in-del | -/A | 0.499113 | 0.0210409 | intron-variant | LONRF3 | GRCh38.p7 | X:118998185 | GTTTATGGCAACACA[-/A]TTCACAATTGCAAAA | 79836 |
rs60983434 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | LONRF3 | GRCh38.p7 | X:118995397 | AAAAGTCTGAAAGAG[C/T]ACAAACAGACAATCT | 79836 |
rs61730253 | snp | C/G | 0.0314918 | 0.121467 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975145 | AAGGCGAGGCGCTGG[C/G]GCCGGCGCCCCCGGA | 79836 |
rs61733808 | snp | A/G | 4.57807e-05 | 0.00478417 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014307 | TATCCCTAAAGAATC[A/G]GATACTCAATCACTT | 79836 |
rs62599016 | snp | A/G | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118983205 | CTTCTTTGACTCAGG[A/G]TCTGGATTGTCAGTG | 79836 |
rs62599018 | snp | C/G | 0.260806 | 0.249766 | intron-variant | LONRF3 | GRCh38.p7 | X:119001189 | CTAGTCAAGTTCTCT[C/G]TGTCTCTCTCTTTTT | 79836 |
rs67313203 | in-del | -/T | 0.386699 | 0.209316 | intron-variant | LONRF3 | GRCh38.p7 | X:118988814 | CCAGGTGATTTTGTC[-/T]TTTTTTTTTTTTTTA | 79836 |
rs72404798 | in-del | -/T | 0.0719118 | 0.175455 | intron-variant | LONRF3 | GRCh38.p7 | X:119004101 | ATAATGACAGATTTG[-/T]TTTTTTCCTCTCCAG | 79836 |
rs73602815 | snp | C/T | 0.0235569 | 0.105941 | intron-variant | LONRF3 | GRCh38.p7 | X:119002311 | TTTTAGCTTTACTAC[C/T]CGAATATGTGTATCT | 79836 |
rs73637820 | snp | C/G | 0.0728917 | 0.176444 | intron-variant | LONRF3 | GRCh38.p7 | X:119002285 | TATCTTGACTTTTAT[C/G]TTGTTTCTCTTTTTA | 79836 |
rs76155459 | snp | G/T | 0.00191645 | 0.0308959 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989550 | AAGAGGAGGAGAAGT[G/T]GGATGCTACCTCTCC | 79836 |
rs77839168 | snp | A/C | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118993123 | GGTTATTCTAACACC[A/C]CCCCCCAAAAACCAC | 79836 |
rs79556072 | snp | G/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118995051 | CATTCTATTCAACAG[G/T]GCATGAAACTTTCTC | 79836 |
rs79981574 | snp | G/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:119000556 | ATTTGCCTCGTGTGG[G/T]TACCTTAGCCATTGG | 79836 |
rs80096503 | snp | G/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118979016 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTTTC | 79836 |
rs111434717 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012104 | AATATGAGCATTTGT[A/G]AGGATCATTGTCCCT | 79836 |
rs111448262 | snp | A/G | 0.000115908 | 0.00761188 | intron-variant | LONRF3 | GRCh38.p7 | X:118978341 | TTCTTTCTTATTTTG[A/G]CAGCTCCAAATGACC | 79836 |
rs111514403 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118996844 | GGAGAATGGTGTGAA[C/T]CCAGGAGGCGGAGCT | 79836 |
rs111621670 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118991559 | AATTATTCACATGCT[C/T]CCCCACCCCAAAAGA | 79836 |
rs111782759 | snp | C/T | 0.0414859 | 0.13792 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018872 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 79836 |
rs111846295 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119010048 | GGTGCTGGGATTACA[A/G]GCGTGAGCCACCATG | 79836 |
rs111850652 | snp | C/G | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118983012 | CTTATCTAGGAAGGG[C/G]AGTGAGGGTGCTGTC | 79836 |
rs111890337 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986587 | TGCAGATATTTCTGC[A/G]GAGTGTTAGCACTAG | 79836 |
rs111923979 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975945 | GTATCTTTGTCACTG[C/T]TTCTTTCTTTTTCGG | 79836 |
rs112069033 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013666 | TCCCCTAAGGCAGAA[A/G]GATGACACATCTAGT | 79836 |
rs112106397 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118994603 | AGACTGGGTTTCACC[A/G]TGTTGGTCAGGCTGG | 79836 |
rs112242338 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:118998455 | GGACTTGGGGACTTG[C/G]GGGGAAAAGTGGGAA | 79836 |
rs112318061 | snp | C/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118992693 | TTCTGGAAAGCACCA[C/T]CTCCTGGCAGGAGAC | 79836 |
rs112411266 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | LONRF3 | GRCh38.p7 | X:119016788 | AGTGACATGGTATAC[A/G]TGGACTATTGCCTTC | 79836 |
rs112420350 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979609 | TAAATGTTTTCTATC[A/G]CCATTTTTATCATTT | 79836 |
rs112467015 | snp | A/C | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118982707 | AGGGCTGTAGATAAG[A/C]GAGTCCTTTTAAAAT | 79836 |
rs112509342 | snp | C/T | 0.00011859 | 0.00769942 | intron-variant | LONRF3 | GRCh38.p7 | X:118978301 | CTTAACACCTGCTTG[C/T]GCTGGGGGCCATTAA | 79836 |
rs112571641 | snp | C/T | 0.003943 | 0.0442262 | intron-variant | LONRF3 | GRCh38.p7 | X:119009274 | CATATTTCTGTTTTG[C/T]TTCACTCATACCAGC | 79836 |
rs112596896 | in-del | -/A | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118999157 | GACCTTCTTTCTCTT[-/A]AAAAAAATTTTAGGT | 79836 |
rs112722330 | snp | A/C | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118991883 | TTTTTTCCTTGTAGA[A/C]CAGAGGTCCAGAAGG | 79836 |
rs112734697 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977644 | CCTTCTCTGGGCTTG[A/T]TTTTCCCATCTGAAG | 79836 |
rs112745813 | snp | A/G | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118988843 | CCAAATCTAGTAAAA[A/G]GAATAGTTTGTACCT | 79836 |
rs112748076 | snp | C/G | | | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976164 | GTTGCCCCTTCCGGG[C/G]CCGCGGCTCCCTGTG | 79836 |
rs112760745 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118994505 | GCCACCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 79836 |
rs112931047 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:118998170 | GATACTTGCACATGC[A/G]TGTTTATGGCAACAC | 79836 |
rs112948719 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | LONRF3 | GRCh38.p7 | X:118991560 | ATTATTCACATGCTC[C/T]CCCACCCCAAAAGAA | 79836 |
rs113110467 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | LONRF3 | GRCh38.p7 | X:118986686 | GGGCCACACTCCAGA[C/T]CTGGGGGAGATGGGA | 79836 |
rs113129534 | snp | C/G | 0.0068637 | 0.0581785 | intron-variant | LONRF3 | GRCh38.p7 | X:118992672 | CACACTACCACAGCT[C/G]TTGTTTTCTGGAAAG | 79836 |
rs113178563 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993625 | AATAATCGAGGAAAA[C/T]TTCCCCGGCCTTGTG | 79836 |
rs113202712 | snp | A/C | 0.5 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:119001097 | TGTTTTTTGTGTGAA[A/C]ATCTGGCCCTGCTCT | 79836 |
rs113287110 | snp | C/G | 0.00791544 | 0.0624105 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975668 | CGGGAGAACAAACCC[C/G]GCAGCGAGAAGGGAT | 79836 |
rs113332628 | snp | C/T | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:119016354 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 79836 |
rs113388501 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994238 | CCCACTTAAAAGATA[-/C]AGAACCGCAGAATGG | 79836 |
rs113436385 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118991786 | TACTCCATAGGGTTG[C/T]CATGATTAATTGAGA | 79836 |
rs113464321 | snp | C/T | 0.000767902 | 0.0195796 | intron-variant | LONRF3 | GRCh38.p7 | X:118987121 | TCGTGACGCTTCGTT[C/T]GGCTGTTTTGTGGGC | 79836 |
rs113491845 | snp | A/C | | | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975643 | GGGGCTCGGTGGCTA[A/C]ATGAGGGAGCGGGAG | 79836 |
rs113526760 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:118994456 | TCACCCAGGCTGGAG[C/T]GCAATGGTGTGATCT | 79836 |
rs113582017 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118991583 | CAAAAGAAAGAGGCT[A/G]TGATTATGGTGTGTG | 79836 |
rs113640787 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997379 | AGTGGGGAAAGGACA[A/C]CCTTTTCAACAAATG | 79836 |
rs113818998 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019024 | ATGCCTGTAATCCCA[G/T]CTACTTGGGAGGCTG | 79836 |
rs113827748 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996779 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCATGC | 79836 |
rs113882321 | snp | C/T | 0.000105669 | 0.00726797 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974779 | CCCGTGTCCCTCTTC[C/T]CATGGAGTCAGTACG | 79836 |
rs113884820 | snp | A/G | 0.0194105 | 0.0965841 | intron-variant | LONRF3 | GRCh38.p7 | X:119002112 | GAAATACACACAGTG[A/G]AAAAGTGCATAAAAT | 79836 |
rs113942247 | snp | A/G | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:119008446 | GGACAGGGGTGTTTG[A/G]GAGGAGAGTAACAGT | 79836 |
rs115221783 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006385 | CCCTCAAACCATCTA[C/T]TTCTCCTGTCTTCTT | 79836 |
rs116818659 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:118980059 | CTGCCCTGATTGCCT[C/T]GCAATGATGCAATGA | 79836 |
rs137993161 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002262 | ACTATCCTCCCTACC[C/T]CAACCACTATCTTGA | 79836 |
rs138074567 | snp | A/G | 0.080205 | 0.183493 | intron-variant | LONRF3 | GRCh38.p7 | X:118997048 | AATACTGTGAAAACG[A/G]CCATACTGCCAAAAG | 79836 |
rs138266231 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983678 | TAATCGGCCTGTAAG[C/T]TGGATTCTGACAGTT | 79836 |
rs138316235 | snp | C/G/T | 5.09317e-05 | 0.00504616 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989619 | AGAAAAGGAAACATT[C/G/T]CCAGATTGAATCCCA | 79836 |
rs138448277 | snp | C/T | 0.0250562 | 0.109088 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974766 | CGCCTCGTCTCCTCC[C/T]GTGTCCCTCTTCCCA | 79836 |
rs138618352 | in-del | -/TTTC | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016343 | TATTTCTTTCTTTCT[-/TTTC]TTCTTTCTTTTTTTT | 79836 |
rs138630765 | snp | A/T | 0.0214859 | 0.101397 | intron-variant | LONRF3 | GRCh38.p7 | X:119001788 | TATTCATCTGCTCAC[A/T]AAATGTCAGTATTTA | 79836 |
rs138647528 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118996454 | CTAGAACTGACAAAA[G/T]AATTCAGTAAGGTTT | 79836 |
rs138678044 | snp | G/T | 0.0738704 | 0.177421 | intron-variant | LONRF3 | GRCh38.p7 | X:118993435 | AAGAAATTCAGAGCT[G/T]GAAGACAAGGTCTTC | 79836 |
rs138727666 | snp | G/T | 0.0131573 | 0.0800346 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018475 | ATATAAAATACTTAA[G/T]GGATTTGGCCTAGAT | 79836 |
rs138746007 | snp | A/C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988657 | TATGGGTTTAGATTA[A/C/G]AGAGGGGTTCTCCAT | 79836 |
rs138914918 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119005778 | CAGGTGAACAGGTTG[A/G]CTAAATATTTTCGGA | 79836 |
rs138968527 | snp | A/G | 0.022522 | 0.1037 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012375 | TGGGTTTGCTTGGAA[A/G]ATTGGTGAGTTAATA | 79836 |
rs139093891 | snp | C/T | 6.86821e-05 | 0.00585972 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011817 | CTCTTTCTGACAGCC[C/T]TAATAAGAATGTGCC | 79836 |
rs139107323 | snp | A/G | 6.93995e-05 | 0.00589024 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014336 | TTTGGTCCCATGCCG[A/G]AGAAAGACGCCGATC | 79836 |
rs139152489 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | LONRF3 | GRCh38.p7 | X:118986622 | GTGGCTCTTAACCTT[A/G]GCTAGGCAACAGAGG | 79836 |
rs139175924 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018443 | GTCCACTTTTTTTTT[-/T]CAGTTTGAACTAAAC | 79836 |
rs139410070 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | LONRF3 | GRCh38.p7 | X:119000141 | ATGATTGGTTCTCTT[A/G]TTACCCTCATGTGTC | 79836 |
rs139436051 | snp | A/C/G | 0.000253979 | 0.0112663 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975349 | GGCGGGCCGCCGACC[A/C/G]GCGCTGTGCGCTGTG | 79836 |
rs139684249 | snp | A/C/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119014484 | GATGGATTTAATTTG[A/C/G]TGTTGTTTGGCTGCA | 79836 |
rs139795843 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118987107 | CTCACCCAGCTCGCT[C/T]GTGACGCTTCGTTTG | 79836 |
rs139969295 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | LONRF3 | GRCh38.p7 | X:118989976 | GCCACTTCCTTCTAG[A/G]TCAGCCTCTTGCTAC | 79836 |
rs140179137 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | LONRF3 | GRCh38.p7 | X:119008965 | ATGAAACTAACATCC[A/G]GAAAATACATATATT | 79836 |
rs140198735 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119003142 | TTATAGACAGGGTCA[C/G]AATTCATTTTTTTTA | 79836 |
rs140224937 | snp | A/G | 0.00331959 | 0.0406051 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978451 | ATGTAAGCTCCGCCC[A/G]ATGGGTTTTAAGGTG | 79836 |
rs140267054 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119015662 | AGGCAAAAGATACAG[A/G]TCAGCAATGGTAACG | 79836 |
rs140414620 | snp | G/T | 0.0001478 | 0.00859523 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989589 | CTTCCAGCAAGACTG[G/T]AAAATGCCAGGAAAA | 79836 |
rs140458588 | snp | C/T | 0.10554 | 0.204037 | intron-variant | LONRF3 | GRCh38.p7 | X:118992335 | CTGTTGGGGAGGGCA[C/T]GGTGGAAGTGAGACT | 79836 |
rs140509616 | snp | C/T | 0.0204488 | 0.0990265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977676 | ATGGGTTGATTGAGC[C/T]AGATAATCTCTAATA | 79836 |
rs140562066 | snp | A/G | 0.0384368 | 0.133195 | intron-variant | LONRF3 | GRCh38.p7 | X:118988028 | AAGTTGAGGATCAGA[A/G]GCGCAGACTCCAAGG | 79836 |
rs140626160 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119000910 | CCCCTCCCTCCTCTC[C/G]TCCTCCTTTCCTCTT | 79836 |
rs140861843 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119001494 | TTACCACCTCTTAAT[A/G]TACAAAGTTAAGTAT | 79836 |
rs140887919 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:118999166 | AAAAAAATTTTAGGT[A/G]CCAGATTTTCTCATA | 79836 |
rs140894602 | snp | G/T | 0.000537722 | 0.0163882 | intron-variant | LONRF3 | GRCh38.p7 | X:118978330 | AATAAAGGTTTTTCT[G/T]TCTTATTTTGACAGC | 79836 |
rs140924738 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118995109 | AATGAGCCTCACTAA[A/G]TTTAAGAGAACTGAA | 79836 |
rs141017294 | snp | A/C | 6.85338e-05 | 0.00585339 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989456 | GAGGAAGCAGCAGCC[A/C]GGGGAGATGGCAGCA | 79836 |
rs141494261 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118984082 | CTGCATTATACACTG[C/T]GCTAGGCATTTTATG | 79836 |
rs141620497 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | LONRF3 | GRCh38.p7 | X:118994177 | AATGAATGCTACGGT[A/G]CGGTACACCACATTT | 79836 |
rs141656175 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | LONRF3 | GRCh38.p7 | X:119007511 | GAAGACCTGAGAATC[C/T]ATCTTGTTTTCCCTC | 79836 |
rs142033809 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119017407 | GGGGGAAAATAGATA[C/T]AGGGTCAATTAGCAA | 79836 |
rs142205167 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118977780 | TGTCCAAGTTCATTT[A/G]CATTTGGCCATTTGA | 79836 |
rs142382955 | snp | C/G | 0.00065197 | 0.0180433 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974917 | TGGCTGCAGAGGGCC[C/G]CGCACCTCTACCGAC | 79836 |
rs142397401 | snp | A/G | 0.0787474 | 0.182133 | intron-variant | LONRF3 | GRCh38.p7 | X:118999228 | GCAGGTGGAATGTTG[A/G]AGCACTCAAAGCAAG | 79836 |
rs142404250 | in-del | -/GTGT | 0.0728917 | 0.176444 | intron-variant | LONRF3 | GRCh38.p7 | X:119003981 | TAATTGTGTGTGCAC[-/GTGT]GTGTGTATTTATCTA | 79836 |
rs142486104 | snp | A/G | 0.00370173 | 0.0428621 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973751 | CACCGACCCCAGCAG[A/G]CCGGGTACATCCCTG | 79836 |
rs142566551 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118987719 | ACAATCCCTCCTTTC[G/T]AGCTTTTGTTTGTTC | 79836 |
rs142579791 | snp | A/C/G/T | 0.0012371 | 0.0248414 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989647 | CCAAGAAGAAACGGG[A/C/G/T]ATGCCTAATAAAGCC | 79836 |
rs142630608 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118991585 | AAAGAAAGAGGCTAT[A/G]ATTATGGTGTGTGTA | 79836 |
rs142726953 | snp | C/G | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:118998320 | ATTTGCAGTGACCTG[C/G]ATGAGATTGGAGACT | 79836 |
rs142857035 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119009420 | ACAAACCAGGGTTTC[C/T]GCTGCACCCAGAGAG | 79836 |
rs142959659 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119002704 | AGTTCTTTGCTAGTC[G/T]TATGTGTTGCAGATA | 79836 |
rs143167361 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119005699 | GTGCTTAAATGGGTA[A/G]ATGTGTAAGAGAGAG | 79836 |
rs143242087 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981988 | AGCCAAGTTGCTAGT[A/G]TCCACCTGTCTCAAG | 79836 |
rs143377151 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | LONRF3 | GRCh38.p7 | X:118978878 | TTGTGAGGATTACAT[A/G]AGCTAATAATGTAAG | 79836 |
rs143410633 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980461 | TTATCAGAACTTTTT[-/T]GGATCTGGAAACCAG | 79836 |
rs143563076 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119003390 | ACAGCCCACATGGAA[C/T]TGATTTTTGCGAATG | 79836 |
rs143888753 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118980089 | AGGGTCAAAAGTGAA[C/T]GTGGCCAAGAGGACA | 79836 |
rs143959775 | snp | A/G | 2.287e-05 | 0.00338149 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017596 | TTCCCTTGGAAAGCC[A/G]AGCTCAGCTCCCCTT | 79836 |
rs144052230 | snp | C/T | 4.55903e-05 | 0.00477421 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982843 | TCAGAAAAGCCCAAG[C/T]CTTAGCCACCCTAGG | 79836 |
rs144250170 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013799 | ACTGAGTAAATGTGT[C/T]TGACCAAGATAGTTA | 79836 |
rs144350388 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | LONRF3 | GRCh38.p7 | X:118994601 | AGAGACTGGGTTTCA[C/T]CATGTTGGTCAGGCT | 79836 |
rs144692414 | snp | C/T | 0.016289 | 0.0887646 | intron-variant | LONRF3 | GRCh38.p7 | X:118977058 | CAGACTGTGAGCTGC[C/T]ACCAGGCTGGAGTGT | 79836 |
rs144766423 | snp | A/G | 0.0015242 | 0.0275641 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014164 | GACTCTGGGAATGAT[A/G]GAGAGGGTACAGAAT | 79836 |
rs144808950 | snp | A/G | 2.27894e-05 | 0.00337553 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011878 | CGTTCCTTGTCCCCT[A/G]CACATCTTTGAGCCT | 79836 |
rs144976063 | snp | A/G | 0.0245906 | 0.108123 | intron-variant | LONRF3 | GRCh38.p7 | X:119004851 | TTTAAAGATAAAGCT[A/G]TTCAGGTGATTCTGA | 79836 |
rs145103820 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012245 | AGTCAAACTGCCTGC[G/T]TTCATTATCTAGTTG | 79836 |
rs146038035 | snp | C/T | 0.000971581 | 0.0220192 | intron-variant, synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118986981 | TCAGGAACATTCTCC[C/T]GATATCCTGAAGCTG | 79836 |
rs146131391 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008384 | ACATCAGTTGTTTGA[G/T]TCACACCGTTAAATA | 79836 |
rs146143677 | snp | A/G | 0.00025445 | 0.0112765 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014335 | CTTTGGTCCCATGCC[A/G]GAGAAAGACGCCGAT | 79836 |
rs146157216 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119003120 | TCAAAATTATCAATC[C/T]TTTCATTTATAGACA | 79836 |
rs146170211 | snp | C/T | 0.00194486 | 0.0311231 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990479 | TCGCAGATCCTCCCA[C/T]TGATCAGGGGGACAA | 79836 |
rs146290760 | snp | C/T | 0.005915 | 0.0540603 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009146 | GGCATCAAGAAAATA[C/T]AGCAAAAATGTAATA | 79836 |
rs146411319 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:118980923 | GTTTCATTTCCCCAT[A/G]GTGATGAAGTGAGAG | 79836 |
rs146443202 | snp | C/G/T | 0.000801943 | 0.0200085 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989421 | AGGACAATCTGGAGC[C/G/T]CCCACATTGTTCTAG | 79836 |
rs146700534 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | LONRF3 | GRCh38.p7 | X:118982698 | CCGCATTTTAGGGCT[A/G]TAGATAAGAGAGTCC | 79836 |
rs146810978 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119000578 | AGCCATTGGGGGCCA[C/G]CTCTGGGGCTGCTAT | 79836 |
rs147104980 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118988031 | TTGAGGATCAGAAGC[A/G]CAGACTCCAAGGCAG | 79836 |
rs147264586 | snp | A/G | 4.22012e-05 | 0.00459335 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974795 | CATGGAGTCAGTACG[A/G]ATCGAACAGATGCTG | 79836 |
rs147361840 | snp | C/T | 0.0204488 | 0.0990265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002005 | CACAGGACTAAGTTA[C/T]CAAGGAAATGAGATA | 79836 |
rs147604140 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977496 | GATGGCCATTGTGTC[C/T]GTATTATTCCAAGTA | 79836 |
rs148027512 | snp | C/G | 0.000767754 | 0.0195777 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989528 | CACCACATGAAAGAC[C/G]AGGAAGAAGAGGAGG | 79836 |
rs148393727 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118994173 | GCACAATGAATGCTA[C/T]GGTACGGTACACCAC | 79836 |
rs148508913 | snp | A/G | 0.000881348 | 0.0209737 | intron-variant | LONRF3 | GRCh38.p7 | X:119009288 | GTTTCACTCATACCA[A/G]CTCAATGAGAGCTGA | 79836 |
rs148556587 | snp | A/G | 0.00248119 | 0.0351346 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011890 | CCTGCACATCTTTGA[A/G]CCTTGTTACCGCCTG | 79836 |
rs148743474 | snp | C/T | 0.0758246 | 0.17934 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013961 | ATCTCTGGTTTTCTG[C/T]ATGTTTTGCTGTTTC | 79836 |
rs148847602 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987599 | TTGGTTAGATCCAGC[C/T]GAGAGAGATTTTACA | 79836 |
rs149016389 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | LONRF3 | GRCh38.p7 | X:118995462 | CAAACCAAACTCAAA[C/T]CCAGCAGAATAAAGG | 79836 |
rs149036762 | snp | C/T | 0.0425 | 0.139441 | intron-variant | LONRF3 | GRCh38.p7 | X:119010777 | GAGCTGGCTCTGTTT[C/T]GGTTCCCCAACGGGT | 79836 |
rs149218778 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993134 | ACCCCCCCCCAAAAA[-/A]CCACACTAGTTCACC | 79836 |
rs149366556 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | LONRF3 | GRCh38.p7 | X:118988729 | ATCCTTTTTCAAATA[G/T]CCATCTCCTGGGAAA | 79836 |
rs149376734 | snp | C/T | 2.27936e-05 | 0.00337584 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011853 | TCGTGTGTACTATGG[C/T]CTATCCCACCGTTCC | 79836 |
rs149422415 | in-del | -/A/AC | 0.497499 | 0.0352757 | intron-variant | LONRF3 | GRCh38.p7 | X:118993122 | GGTTATTCTAACACC[-/A/AC]CCCCCCCAAAAACCA | 79836 |
rs149610065 | snp | G/T | 0.0142023 | 0.083063 | intron-variant | LONRF3 | GRCh38.p7 | X:119008130 | ACAGATGCTATAGAG[G/T]TCAGGACTTGGGGTC | 79836 |
rs149620973 | snp | C/G | 0.0256233 | 0.11025 | intron-variant | LONRF3 | GRCh38.p7 | X:118978737 | AGCCAGACTGCCTGG[C/G]TTTATGTCCCAACTC | 79836 |
rs150059826 | snp | C/T | 0.000191982 | 0.00979561 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975543 | GGCAACCGACTGTAC[C/T]GCGAGCGCCAGGTGG | 79836 |
rs150063459 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119000300 | AAAAACAAGTTAGAG[A/T]ATGAATTTGTATACA | 79836 |
rs150119195 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119007950 | ACATTTTAGTATGTG[C/T]CTTTTCTGGCTTTTT | 79836 |
rs150168183 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | LONRF3 | GRCh38.p7 | X:119001539 | ATACAGCCAGAAAAA[G/T]ATATTCCATCTGTTC | 79836 |
rs150372102 | snp | A/G | 2.49302e-05 | 0.00353051 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989601 | CTGGAAAATGCCAGG[A/G]AAAGAAAAGGAAACA | 79836 |
rs150516801 | snp | G/T | 0.0787474 | 0.182133 | intron-variant | LONRF3 | GRCh38.p7 | X:118994228 | GCCTAAATGCCCCAC[G/T]TAAAAGATACAGAAC | 79836 |
rs150821531 | snp | G/T | 0.0884172 | 0.190764 | intron-variant | LONRF3 | GRCh38.p7 | X:118979361 | TGCAGTGGCGTGATC[G/T]CAGCTCACTGCAACC | 79836 |
rs150886041 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119000118 | TTCTCTTTCTTGTTG[C/T]TAGGAATATGATTGG | 79836 |
rs150906004 | snp | C/T | 5.43641e-05 | 0.00521336 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975330 | AAACTGTGCCTGGAA[C/T]GTGGGCGGGCCGCCG | 79836 |
rs151046762 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:118996100 | GAGAGTGTTAATCAT[A/G]AAGCGATGCTGGATT | 79836 |
rs151225802 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118977954 | TCAGATAGGGGTCAC[A/G]TCTGCCCACCTCTCT | 79836 |
rs151236086 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118992075 | AGGAGGCTGAGATAT[C/T]TGCACAAAAATTAAG | 79836 |
rs180785047 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119010562 | CTGTAAATTAGCATT[A/G]AGCCTCTCTGAGCCC | 79836 |
rs180786742 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018531 | AATAATTCATTTTCT[A/G]TGTGTAATACAGAAC | 79836 |
rs180790153 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118995378 | TCCCTGAGCACCTAC[A/C]TCAAAAAGTCTGAAA | 79836 |
rs180791984 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980752 | GAGTAAGAGGACTTG[A/C]AACTCTTTCCACCTC | 79836 |
rs180948015 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118985779 | CTGAGCTTTGAAGGC[C/T]GAGTGGGGTTTGGCT | 79836 |
rs180948625 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118999865 | CATACACTGCTAAGT[A/T]ATAGCTGGCCTCTCA | 79836 |
rs181092121 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118980240 | AGACCAGAGGTGTTC[A/T]GAATCCAGAATGTTT | 79836 |
rs181112442 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119009676 | TACCTCAAAGTGAGT[A/C]TACTTCACGACCCTA | 79836 |
rs181136486 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118994496 | GCAACATTCGCCACC[A/G]GGTTCAAGCGATTCT | 79836 |
rs181394783 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997623 | ATAAATAGCTGGGAC[A/G]GCTGGGACCTAACTA | 79836 |
rs181417756 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982504 | TTTGATGGTCACTCC[C/G]TACAATGGTGGGGCA | 79836 |
rs181450596 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119005340 | TTTCTGAAGGTACAG[A/G]ACAAATTTATAAAAG | 79836 |
rs181474873 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119004464 | TTTGAAGACCAATAC[A/G]GTAAGTTTGCCTATG | 79836 |
rs181564375 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014104 | GGGTGAGCCTTCCCA[C/T]AGGAAGGCAGGATGG | 79836 |
rs181595341 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118992090 | TTGCACAAAAATTAA[A/G]ACGGTTGGCAGGCTG | 79836 |
rs181603971 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118991917 | CTTTGGGTCTATGGA[C/T]CTCTGAGGATGTTCT | 79836 |
rs181606896 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | LONRF3 | GRCh38.p7 | X:118977298 | AGGCAGATTCCATAC[C/T]TTTTAGCCATCCCCC | 79836 |
rs181798570 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997968 | ATAAAAAACTCAAAA[A/G]ACAGTAGATGCTGGC | 79836 |
rs181803023 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983506 | ACCATTACAATATAA[G/T]GCAAGCAGTCGTTCC | 79836 |
rs181813575 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982250 | GTGGAGAAGAGCATT[C/T]TGGGAGTCCTGAGAC | 79836 |
rs181823487 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015140 | TCTAGGATAAGGCTG[A/G]AGATATCCTAACCAC | 79836 |
rs181926654 | snp | A/G | 0.000529661 | 0.016265 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990478 | ATCGCAGATCCTCCC[A/G]CTGATCAGGGGGACA | 79836 |
rs182011372 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994384 | AATGAGCAGGGGTAG[A/C]TATTTTTATATCAGA | 79836 |
rs182015326 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119009421 | CAAACCAGGGTTTCC[A/G]CTGCACCCAGAGAGC | 79836 |
rs182075046 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118997259 | AAACAGCATGGTACT[C/T]GTATAAAAATAGGCA | 79836 |
rs182227757 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004178 | ATAGTTTTTCTTTTT[A/T]AAATAACTTTGCTTT | 79836 |
rs182303039 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973230 | GTTCAGAAGCAAAAA[C/T]GATGGATTCTAAAGT | 79836 |
rs182328973 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | LONRF3 | GRCh38.p7 | X:119000324 | GTATACACGGATTCT[A/G]GAGAGAAAATTAGGA | 79836 |
rs182389209 | snp | C/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973492 | GGCAGACAAAGAGTG[C/T]GCAGTTGGCCACCCC | 79836 |
rs182390714 | snp | A/C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987314 | ACAGGGTCTCTTTCT[A/C/G]TCACCCAGGCTGGAG | 79836 |
rs182414609 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119001071 | TACTCCATCACTGTA[A/G]CAATGTAAAATGTTT | 79836 |
rs182517491 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987861 | AATACGTATTTGTAA[A/C]AGAGAAGAGGAAAGA | 79836 |
rs182537969 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118998642 | CAGAAATTAAGAAGA[C/T]TGACCCAAGAGAAAA | 79836 |
rs182544340 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | LONRF3 | GRCh38.p7 | X:119015552 | CCAGCTCCTGGCTCT[A/G]GGCCACGATGAGTCA | 79836 |
rs182548747 | snp | A/G | 0.0101401 | 0.0704787 | intron-variant, synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118986945 | CCTTAGTTTCTTTTC[A/G]CCATCAGTCCCGGGG | 79836 |
rs182596546 | snp | A/G | 0.0026455 | 0.0362733 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019115 | TGCACTCCAGCCTGG[A/G]CAACGAGCAAACCTG | 79836 |
rs182777118 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119001735 | CATTTTAATCACAGC[A/T]TTTGCTAAGAGATTG | 79836 |
rs182828707 | snp | A/G | 0.0240739 | 0.107039 | intron-variant | LONRF3 | GRCh38.p7 | X:118996478 | AAGGTTTCTGGATAC[A/G]AGATTAATGTACACA | 79836 |
rs182972512 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993133 | ACACCCCCCCCCAAA[A/G]ACCACACTAGTTCAC | 79836 |
rs182974088 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007256 | ACTAGGTAAGCCCTG[A/G]TGTTCCCTTATCATC | 79836 |
rs183127586 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118981433 | GAGGTTGTAGTGAGC[C/T]GAGATCCACCACTGC | 79836 |
rs183153388 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118998785 | CATCTCACTGCATCC[C/T]CTGCCTCCCAGTTCA | 79836 |
rs183160176 | snp | A/T | 0.000321776 | 0.0126801 | intron-variant | LONRF3 | GRCh38.p7 | X:119011807 | CTGTCATTTTCTCTT[A/T]CTGACAGCCTTAATA | 79836 |
rs183161876 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977930 | ACTTGGATTTGTCTT[C/T]TTGGTGGTTCAGATA | 79836 |
rs183334180 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118984052 | ATAATAGCTAACATT[C/T]GTTGAGAATTTCTTC | 79836 |
rs183375549 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119015237 | GCTCATCCCCAACTC[A/T]GTCACAAAAGAAAAA | 79836 |
rs183384840 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119011280 | GATTATTCTTGCCTA[C/T]CTCTTGGTCCTTCCT | 79836 |
rs183550978 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118996366 | AATCAGTAAAGAGGA[A/G]CTCAGATTGTCACTG | 79836 |
rs183552256 | snp | C/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974256 | GAGGTACCAGCCTCT[C/T]CTGGGAGGAGTGGGG | 79836 |
rs183557941 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118981203 | TAGAGTATATGGGTT[G/T]GCCGGGCATGGTGGC | 79836 |
rs183596361 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:118996708 | CAGGCAGATCACGAG[A/G]TCAGGAGATCCAGAC | 79836 |
rs183596558 | snp | C/T | 0.00317376 | 0.039709 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012712 | GTGGAGGCCTAATCA[C/T]CTCTTAAATGTCCCA | 79836 |
rs183907358 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119006517 | GCAGTTCTCCTGCCT[C/T]AGCCTCCCAAGTAGC | 79836 |
rs183910514 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984911 | TTGACATTTATAAGC[C/T]GCCTTCGAACTCACA | 79836 |
rs184051552 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003281 | TTGCCTCAGCACCCC[C/T]GCCTCAAGTAGCTGG | 79836 |
rs184059332 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118989201 | CCTAACTCCACCCAA[G/T]CTGGGAATGCCTTGG | 79836 |
rs184061284 | snp | C/T | 0.000198059 | 0.00994939 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975041 | AATCCGTGAAGCCCT[C/T]GAGGTGTATAGACAG | 79836 |
rs184071521 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118988249 | ATAATTAAGATCACT[A/G]TTAAATGATTGAGAA | 79836 |
rs184199217 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999661 | CTTGTTTGTCCTTGA[A/C]CTCAACAGGGGGCTT | 79836 |
rs184218116 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118985739 | TAGAACAGGACTGGA[A/G]TAGTGAGGGAAGGTA | 79836 |
rs184238016 | snp | A/G | 0.0026455 | 0.0362733 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018365 | TCTTAGACCATTTCC[A/G]TATCTATCCAAATGG | 79836 |
rs184291595 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:118980091 | GGTCAAAAGTGAACG[C/T]GGCCAAGAGGACATT | 79836 |
rs184299320 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118989847 | TTCTGTGAGATCATG[C/T]ACAGTGCCTAGCACA | 79836 |
rs184324526 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994460 | CCAGGCTGGAGCGCA[A/G]TGGTGTGATCTCAGC | 79836 |
rs184329250 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119009484 | AAGCATAAGCGAAAC[C/T]AGTGATGAGGGTACG | 79836 |
rs184435485 | snp | A/G | 0.0768 | 0.180282 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976190 | CTGTGGGGTGGGTCC[A/G]GCATGGAATTAGGTC | 79836 |
rs184467798 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003769 | CAAAAATAAACAAAT[C/G]AAATAACCCATTGAG | 79836 |
rs184594270 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118993911 | CAGCCAAGAATTTTG[C/T]ATCCAGTGAAACTAA | 79836 |
rs184596399 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118979485 | TTTTTAGTAGTGACG[A/G]GGTTTTGCCATGTTG | 79836 |
rs184602582 | snp | A/G | 0.00147882 | 0.0271519 | intron-variant | LONRF3 | GRCh38.p7 | X:119009122 | ATTGCCTCCCCCCAT[A/G]TAGTGCTTGGCATCA | 79836 |
rs184736161 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013434 | CATGCATAGGAAATG[C/T]TATCCTAGATCAACC | 79836 |
rs184741374 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996888 | GATCACACCACTGCG[C/T]TCCAGCCTGGGCGAC | 79836 |
rs184787370 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | LONRF3 | GRCh38.p7 | X:118979101 | CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 79836 |
rs184816165 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119008598 | AAATTAAAAGAGAAA[A/G]AATAGGTATATTTGG | 79836 |
rs184895932 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993609 | AAAATGTATTTGGGG[A/G]AATAATCGAGGAAAA | 79836 |
rs185126115 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016843 | CTTAAAAGACATGCA[A/G]AGGTCAAGGGGTCAT | 79836 |
rs185132545 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118985402 | GGCATTTATGGCCCC[G/T]GGTGCTGTGAGTACC | 79836 |
rs185239172 | snp | C/G | 0.0068637 | 0.0581785 | intron-variant | LONRF3 | GRCh38.p7 | X:118999334 | CTACTTCCCTCACCC[C/G]CTCATGATAGAATGG | 79836 |
rs185289892 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118997468 | GTACAAAAATCAACT[A/C]AAGATGGATTAAGGA | 79836 |
rs185291058 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118997722 | AAAATCTTCACTATC[G/T]GTACATCTGACAAAG | 79836 |
rs185296965 | snp | A/G | 2.4099e-05 | 0.00347116 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014185 | GGTACAGAATGTTTC[A/G]CTTCCACTTTGATAC | 79836 |
rs185300995 | snp | A/G | 0 | 0 | intron-variant | LONRF3 | GRCh38.p7 | X:118983284 | GAGGACATTCTGGCT[A/G]TTGATGAGAGATCCA | 79836 |
rs185395052 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013777 | GTAGATTAATAAATA[A/T]CTGATGACTGAGTAA | 79836 |
rs185406282 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118982373 | TTAGTGTAGGTGCTC[C/T]TTCAAGCCACTACTG | 79836 |
rs185441611 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118995611 | GATTTATCAAGGGAA[A/G]AAGAGAGAAAATTCA | 79836 |
rs185441778 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010759 | AAGACAAGGATCCCA[C/G]AAGAGCTGGCTCTGT | 79836 |
rs185458375 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018796 | CTTTTTATTATTAAA[A/G]TGTAAATAAGACAAA | 79836 |
rs185458515 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118981000 | GACGAACTGATGCCT[A/G]TAATTCAAAACCACC | 79836 |
rs185528592 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987349 | GTGATATGATCATGG[C/T]TCACTGCAGCCTCAG | 79836 |
rs185530284 | snp | C/T | 0.00738971 | 0.0603345 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973544 | AGGACACCGTCGAGG[C/T]CCCCTAGCCATTGTA | 79836 |
rs185558663 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118982013 | CTCAAGACACACACA[G/T]AGGGCAGCCCTCTCC | 79836 |
rs185569553 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119001307 | ATGCAGAAATACATG[C/T]ACACATTTGTTGCCG | 79836 |
rs185618271 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119004193 | TAAATAACTTTGCTT[A/T]TTGGCCAATTTGATA | 79836 |
rs185768862 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118992122 | TGTTCGTTGTGCTGG[C/T]GGGTCCTGCGGGGAG | 79836 |
rs185859387 | snp | C/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973392 | CAAGCCTAGTCCCTG[C/T]CTCCCTGCTTGGAGC | 79836 |
rs185891497 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119005619 | CTTCAGGCATTAACA[C/T]TGCTTAGACGAAAAG | 79836 |
rs185975442 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:118977457 | TTACCCTTCTAAGAG[C/G]AAAGGAGGCTCTCTG | 79836 |
rs186005604 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118991966 | ATGTATTAATGTCTC[A/G]AAGTTGTATGTTAAA | 79836 |
rs186007652 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004576 | TCTGATGCCTGTCCT[A/G]TACACTGGGCCTACT | 79836 |
rs186060552 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119000089 | CTTTTGATTCCACCT[C/T]TCCAGTGTTTTTCTT | 79836 |
rs186063807 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | LONRF3 | GRCh38.p7 | X:118978094 | CACCACTGACACCAC[A/G]GGGCCTCTAATGAAC | 79836 |
rs186287472 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976813 | TCTGGCGAAGCATGC[C/T]GGGGAGGAGGCAGCA | 79836 |
rs186291001 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991342 | TCCCAGCACTAATCT[A/C]AGTTACATGGGCAAG | 79836 |
rs186375896 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980316 | AGCTTCCTGTAATCC[A/G]ACACACTATTCAGCA | 79836 |
rs186395608 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119009756 | AGAATAATTTAATAA[C/T]TTGAGTTCTTACCTC | 79836 |
rs186485379 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015618 | CAAGCTTAATGTTCC[C/T]CTTCACCTTCCGGGA | 79836 |
rs186496122 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998668 | GAAAATATAACAAAA[C/G]TCTTTTTATTTATTT | 79836 |
rs186507349 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015143 | AGGATAAGGCTGGAG[A/G]TATCCTAACCACATA | 79836 |
rs186559419 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019129 | GGCAACGAGCAAACC[C/T]GCGTCTCAAAAAAAA | 79836 |
rs186626731 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118994506 | CCACCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 79836 |
rs186745461 | snp | A/G | 0.0230396 | 0.104828 | intron-variant | LONRF3 | GRCh38.p7 | X:118987283 | TTTATTCATTACATT[A/G]AAAAAAAATTATGAA | 79836 |
rs186784310 | snp | C/G/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119000397 | GAATGGAACAATAAT[C/G/T]GGAGGTGTGTAAGTG | 79836 |
rs186785013 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981711 | GGAGCTGGGGGAATG[C/T]GGAAAGGTCTTCAAG | 79836 |
rs186822789 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:118996748 | TACCACAAAGAAATC[C/T]TGTCTCTACTAAAAA | 79836 |
rs186825257 | snp | C/T | 2.45592e-05 | 0.00350414 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012936 | GAAAATAGGCAGAAG[C/T]CCCTTGAGCCACAGC | 79836 |
rs186946426 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | LONRF3 | GRCh38.p7 | X:118998500 | AAAGACTACAAATAC[A/G]GTGCAGTGTATAATG | 79836 |
rs187109565 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118984385 | TCCAGGATGAACAAA[A/G]GCAGTTAGAAGAAAC | 79836 |
rs187149453 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119015365 | CATCTCTGACATGAG[A/G]AGGGTTCTAAAGCCC | 79836 |
rs187273456 | snp | G/T | 0.00633741 | 0.0559334 | intron-variant | LONRF3 | GRCh38.p7 | X:118983546 | GTCCCAGCAGAATGT[G/T]GTAGTTATAAAAGAA | 79836 |
rs187352065 | snp | A/G | 0.01368 | 0.0815649 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974273 | TGGGAGGAGTGGGGG[A/G]CCGCTGGTCAGCGGC | 79836 |
rs187387891 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119011369 | TAGGGACCTTACAGA[C/G]AATTTCCCACCACCC | 79836 |
rs187390740 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118988468 | GGTTGTAGTATTGCT[G/T]TAGTGCTGGAGAAAA | 79836 |
rs187458840 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993619 | TGGGGGAATAATCGA[A/G]GAAAACTTCCCCGGC | 79836 |
rs187462531 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998259 | AACTCTGGTATATAT[A/G]TACAATTGAATACTA | 79836 |
rs187643494 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993330 | TAGCTTAAAGAAAAA[A/G]CAATAAAAAATTCAG | 79836 |
rs187652512 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119007732 | CCCTGAGGGTATGCG[C/T]TGGGATTGGGAGGAG | 79836 |
rs187703272 | snp | G/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974129 | GGTTGTGTGTGTGTG[G/T]GGGGGCTTCACGGAT | 79836 |
rs187739106 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119008669 | GACAGGGCAGGAAAG[G/T]TTCAGTGATTGAAAA | 79836 |
rs187752625 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119001746 | CAGCTTTTGCTAAGA[A/G]ATTGCTGTGTCCTTT | 79836 |
rs187903437 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012024 | GTAATGAGGGATTTC[C/T]GTTTTACTTTGGGGT | 79836 |
rs187977368 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119006943 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 79836 |
rs187986963 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118993031 | ACAACAGCCTTTAGC[C/T]CTAGACCTTCCCTCT | 79836 |
rs188030442 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | LONRF3 | GRCh38.p7 | X:118988032 | TGAGGATCAGAAGCG[C/T]AGACTCCAAGGCAGA | 79836 |
rs188064308 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981461 | TGCACTCCAGCCTGG[A/G]TGACAGAGCAAGATT | 79836 |
rs188151534 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118999825 | CAAAACAAAACAAAA[C/T]CCTCTGTGCCTGGAG | 79836 |
rs188159543 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118985777 | AGCTGAGCTTTGAAG[A/G]CTGAGTGGGGTTTGG | 79836 |
rs188174577 | snp | C/T | 0.00844089 | 0.0644143 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018434 | GTCTTCAGAGTCCAC[C/T]TTTTTTTTTCAGTTT | 79836 |
rs188286807 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118997726 | TCTTCACTATCTGTA[C/T]ATCTGACAAAGGACT | 79836 |
rs188327106 | snp | C/T | 0.00112855 | 0.0237277 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014257 | ACATAACTGTGTCTA[C/T]CAGCAAGCATCATTG | 79836 |
rs188345255 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996572 | ACAATAGCTGCAAAA[A/C]AATAAAATATTTAGG | 79836 |
rs188490945 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119002577 | TCATGGACAACATTG[C/T]TATAAACATTGTTTA | 79836 |
rs188584493 | snp | A/G | 0.000307252 | 0.0123908 | intron-variant | LONRF3 | GRCh38.p7 | X:118989378 | ATTAGTCCTAAGAAG[A/G]TTCTGATATGTGGCC | 79836 |
rs188586219 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | LONRF3 | GRCh38.p7 | X:119003362 | TATTGTTCTGCTTTT[C/T]ACATTTATTTTTACA | 79836 |
rs188685396 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016668 | GAATATATTTCTAAT[A/G]TGAATGTTTTCTAAT | 79836 |
rs188693460 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118985063 | ATTCTCACTGAGAAT[C/T]GACCCCAACTTTTGT | 79836 |
rs188800516 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118991353 | ATCTCAGTTACATGG[G/T]CAAGAGCTCAAAGTT | 79836 |
rs188802183 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118977289 | AGATCTCTAAGGCAG[A/T]TTCCATACCTTTTAG | 79836 |
rs188839248 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119004313 | AATACATGAAAAGTC[G/T]CTCTCCTCCTCCAGA | 79836 |
rs188941027 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | LONRF3 | GRCh38.p7 | X:119009508 | GGGTACGCCCTGCCC[C/T]CAGTAACAGGGTATT | 79836 |
rs188976057 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999027 | CTCAGATATTTCCTC[A/G]CCCTTTATGAGCACA | 79836 |
rs189192099 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119003985 | TGTGTGTGCACGTGT[C/G]TGTGTATTTATCTAG | 79836 |
rs189238665 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | LONRF3 | GRCh38.p7 | X:118979638 | TTTCCAGGGACATTA[A/G]AAAGAGGAAGGTGAG | 79836 |
rs189257468 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118985509 | CTGAGGACTTTGGGC[A/C]TGAATGCTAGGCCTC | 79836 |
rs189267989 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118994205 | TTTCAATACTAACAA[C/T]GTAAATGGCCTAAAT | 79836 |
rs189363655 | snp | A/G | 0.00317376 | 0.039709 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976570 | GGCTACGAATGGGTC[A/G]CGCCTCTGTCCCGCT | 79836 |
rs189508460 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013938 | TGCCTCCACTCAGGC[C/T]GGTTTGAATCTCTGG | 79836 |
rs189518586 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118982424 | GAGACTAGTTCAAAC[A/G]AACGCATACCTGGGC | 79836 |
rs189632583 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118989927 | ATCAGGTCAAGCACA[A/G]TATCAACTAATGACA | 79836 |
rs189777188 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118997575 | AAGGATTTCATGACC[A/G]AGAACCGAAAAGCAA | 79836 |
rs189862519 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118983327 | ACCTGCTGTTACATA[A/T]CTTTTCTTTGGCTGA | 79836 |
rs189865168 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118997176 | CAAAGCAAGACTAAG[C/T]AAAAAGAACAAATCT | 79836 |
rs190069045 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984391 | ATGAACAAAGGCAGT[C/T]AGAAGAAACTTATCT | 79836 |
rs190073690 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118982057 | TTTCTTCCTTCTTCC[C/G]CAGGATGTTCCTCTG | 79836 |
rs190077515 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119005004 | TGTGGACCTCAGGTT[A/C]ATTCTAGTTAGTGGG | 79836 |
rs190096671 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:118998515 | GGTGCAGTGTATAAT[A/G]CTCGGGTGATGGTGC | 79836 |
rs190164858 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118980117 | ACATTCTGCAAGCTA[C/T]AAAGCTTCCTGGATG | 79836 |
rs190166739 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118999451 | TGGCTCTAAGCCCAT[G/T]ATGTGCGCTGTGGAG | 79836 |
rs190221011 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987543 | AAGTGATCCTCCCAC[C/T]TTGGCCTTCCAAAGT | 79836 |
rs190226937 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:119001626 | GTATTGAAAAGTGTA[A/C]TGTATTCTAAGCATC | 79836 |
rs190253034 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118994468 | GAGCGCAATGGTGTG[A/G]TCTCAGCTCACTGCA | 79836 |
rs190313848 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118986756 | TTGATTCTGATGCCC[A/G]CTGAAGCGAGGACCC | 79836 |
rs190359466 | snp | C/T | 0.00475684 | 0.0485365 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019075 | CCTGGGAGATGGAGG[C/T]TGCAGTGAGCCGAGA | 79836 |
rs190418735 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119017280 | AGGTTACACATATCA[C/T]TTCCCTTTACATCTC | 79836 |
rs190511972 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987292 | TACATTGAAAAAAAA[A/T]TATGAAACAGGGTCT | 79836 |
rs190518300 | snp | G/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973443 | TGTCTGCTCATTTGT[G/T]AGCTTGGTTCCCGTC | 79836 |
rs190539043 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | LONRF3 | GRCh38.p7 | X:119000849 | TCTCTCACTGTCACT[C/T]TCTCTTCCTCCCTCC | 79836 |
rs190569351 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000239 | ATTTGTACTACTTGT[G/T]CAAGATTTTAGTATG | 79836 |
rs190574047 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972680 | CCATCCCCTCAACCC[C/T]GGTTCAAGCCACCAT | 79836 |
rs190668011 | snp | A/C/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973723 | TGCCACTCTCCCACG[A/C/T]CCCCAGAGTACCCAC | 79836 |
rs190677930 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994899 | AATAGTGAGGGACTT[A/C]AGTACTCCACTGACA | 79836 |
rs190805949 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005627 | ATTAACATTGCTTAG[A/G]CGAAAAGAGGAATCA | 79836 |
rs190921364 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119009862 | GCAACCTCCGCCTTC[C/T]GGGTTCAAGCGATTC | 79836 |
rs190928338 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118980461 | TTATCAGAACTTTTT[G/T]GGATCTGGAAACCAG | 79836 |
rs190990347 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996166 | CATGTGATTTTTGTT[C/T]TGATTTCTTTTCAGT | 79836 |
rs190995401 | snp | C/T | 0.0772873 | 0.180749 | intron-variant | LONRF3 | GRCh38.p7 | X:119011108 | GACAGAGTGAGACTC[C/T]GCTTAAAAAAAAAAA | 79836 |
rs191011116 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118981042 | TTTGCATATTTCCCA[A/C]CATTTCTATGTAAAA | 79836 |
rs191078283 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992606 | GTAGTGGAAGACAAA[G/T]GGCATATAATCTTGG | 79836 |
rs191139992 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993069 | CCTACCCAAATGAGA[A/G]GGAACCAGAAAACCA | 79836 |
rs191145409 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119006992 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 79836 |
rs191147995 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:118992023 | CACATCCTTTAGCAG[A/T]TTCACAAATGTGTCT | 79836 |
rs191155769 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118978604 | AGCCAGGGTAAAGAT[A/C]CCTGGGCAAAGAGTG | 79836 |
rs191176612 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119015437 | TTCCCTAAATGAAAT[A/G]TCTTGCTTTCCTCAG | 79836 |
rs191309622 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984734 | GCCCGTGATGAGTGT[C/T]ACAGAGTTCTGAAGT | 79836 |
rs191335120 | snp | C/G | 0.0068637 | 0.0581785 | intron-variant | LONRF3 | GRCh38.p7 | X:119016274 | AGCTGCTTTGGGGAA[C/G]GATTTATGTGGAATG | 79836 |
rs191337055 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | LONRF3 | GRCh38.p7 | X:118979355 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 79836 |
rs191350574 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977625 | ACCTTGAGAAAATGC[A/C]TTCCCTTCTCTGGGC | 79836 |
rs191353484 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118998744 | TCTCACTTTGTCACC[C/T]GGGCTGGAGTGCAGT | 79836 |
rs191464684 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998272 | ATATACAATTGAATA[C/T]TATGCAGCCATAAAA | 79836 |
rs191617773 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999596 | TTTTCTCTGAAAACT[A/G]AGAATCCTGAGGTGT | 79836 |
rs191633697 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118985622 | CTCTAGAAGCTGGCC[A/G]TCTGGCAGGAGAGAA | 79836 |
rs191646019 | snp | C/T | 2.40584e-05 | 0.00346823 | intron-variant | LONRF3 | GRCh38.p7 | X:119017484 | TGGAACTCTGCAGAC[C/T]GATGTTCTTGGATGG | 79836 |
rs191649557 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119011731 | TCTGCCTTCCCCCAG[G/T]GGTATCACATGCTAA | 79836 |
rs191716317 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983992 | TGCTTCAAGCTGTGG[A/G]CCCTTCTCCAAATCT | 79836 |
rs191795670 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118981552 | GATCACACAGAGGCC[C/T]TTCCAGTCTCCCAAC | 79836 |
rs191889706 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119003750 | ATCAACTTGTCAAGT[C/T]CTACAAAAATAAACA | 79836 |
rs191903777 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019343 | AGTACCACAAGTATG[A/G]GAGTGTTATAATGGC | 79836 |
rs191912579 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996430 | CCTAAGGACTCCTCT[A/G]GAAAGCTCCTAGAAC | 79836 |
rs192217713 | snp | A/T | 0.0110639 | 0.0735497 | intron-variant | LONRF3 | GRCh38.p7 | X:119002806 | TTGTTTTTTTATTTT[A/T]TTTTTATTTTGAGAT | 79836 |
rs192228623 | snp | C/T | 0.00317376 | 0.039709 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974590 | CGTGGTACCGTTTTA[C/T]ATAACACTTTGCTGA | 79836 |
rs192231069 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988863 | AGTTTGTACCTTGTT[C/T]ATTTGACCAGTGTAA | 79836 |
rs192300337 | snp | A/C/T | 7.157e-05 | 0.00598163 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013212 | AAAAGGTAAGGGTGG[A/C/T]CAGTGCCAAGAATCC | 79836 |
rs192311972 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | LONRF3 | GRCh38.p7 | X:118996767 | CTCTACTAAAAATAC[A/G]AAAAATTAGCCGGGC | 79836 |
rs192407644 | snp | A/T | 0.0115877 | 0.0752302 | intron-variant | LONRF3 | GRCh38.p7 | X:119008902 | ACCCCCTTGTTAAAA[A/T]TTTTTTTCTAATTAT | 79836 |
rs192471010 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981803 | CATAGCCTGAGGGCT[C/T]TGGGGCCTGCAAAGA | 79836 |
rs192688772 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118993423 | ACAAGTAGAAGAAAG[A/G]AATTCAGAGCTTGAA | 79836 |
rs192744993 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118993867 | GGGACTGGGGACCTA[C/T]CTTCAGCCTCCTCAA | 79836 |
rs192758461 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:118996650 | AACACAGGCCAGGTG[C/T]GGTGGCTCATGCCTG | 79836 |
rs192822535 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008337 | ACTGTAGGGGTAGTT[C/T]CCATAGCAAGCAATT | 79836 |
rs192908050 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979086 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAC | 79836 |
rs192941889 | snp | A/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013762 | TACATTTGTTACATA[A/G]TAGATTAATAAATAT | 79836 |
rs192976334 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118989737 | CACCAATATATACAA[A/G]TTACTTACCTCTGTC | 79836 |
rs192986439 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012260 | TTTCATTATCTAGTT[A/G]CAGCCTTGGAGCAAG | 79836 |
rs193094183 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988056 | AGGCAGAGTTTAGCA[C/T]TGAATGCCTGGGCAT | 79836 |
rs193136847 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118999058 | TATGCTTCTCATATC[A/G]ATCATGTGCATTTGT | 79836 |
rs193241628 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974149 | GCTTCACGGATACCC[C/T]TCCCAACCTGCTTCC | 79836 |
rs193248846 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119002093 | GAAAAACATTTTAAA[G/T]TGTGAAATACACACA | 79836 |
rs193288260 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985401 | TGGCATTTATGGCCC[C/T]GGGTGCTGTGAGTAC | 79836 |
rs199530252 | snp | C/T | 0.00095829 | 0.0218684 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017723 | AGGAGCTCCCACCTT[C/T]CCCACTGCCGTCGGG | 79836 |
rs199619385 | in-del | -/GTAGAC | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999466 | GATGTGCGCTGTGGA[-/GTAGAC]TTGACTTAGCCTGCT | 79836 |
rs199735911 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011021 | CAGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 79836 |
rs199774381 | in-del | -/TG/TGTA/TGTG | 0.0799064 | 0.183948 | intron-variant | LONRF3 | GRCh38.p7 | X:119005428 | ATTGAAGTATATGTA[-/TG/TGTA/TGTG]TGTATATATATGTAT | 79836 |
rs199972979 | snp | A/G | 0.00393967 | 0.0442076 | intron-variant | LONRF3 | GRCh38.p7 | X:118989717 | TTGGAGGAGATCCCC[A/G]GGCTCACCAATATAT | 79836 |
rs199994110 | in-del | -/C/CTTA/CTTT/CTTTC | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016353 | TTTCTTTCTTTCTTT[-/C/CTTA/CTTT/CTTTC]TTTTTTTTTTTTTGA | 79836 |
rs200074995 | in-del | -/TG | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974117 | GGGCTGGGACTGGGT[-/TG]TGTGTGTGTGGGGGG | 79836 |
rs200257474 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018280 | GTTTACCATGTACCT[A/G]GGGGGAAATAACAAT | 79836 |
rs200420551 | in-del | -/TGTA | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003988 | GTGTGCACGTGTGTG[-/TGTA]TTTATCTAGTAACTT | 79836 |
rs200450796 | in-del | -/TAGACT | 0.0728917 | 0.176444 | intron-variant | LONRF3 | GRCh38.p7 | X:118999467 | ATGTGCGCTGTGGAG[-/TAGACT]TGACTTAGCCTGCTC | 79836 |
rs200462697 | in-del | -/CA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993121 | AGGTTATTCTAACAC[-/CA]CCCCCCCCAAAAACC | 79836 |
rs200569560 | snp | C/T | 0.000259082 | 0.0113787 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974848 | GCGACAACTTGGAGT[C/T]GGCGGAGCGAGGGGC | 79836 |
rs200596879 | in-del | -/ACACACACACAC | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986052 | TTTCAGTATATGGAA[-/ACACACACACAC]ACACACACACACACA | 79836 |
rs200671696 | in-del | -/TCTCTCTCTCTCTCTCTCTCTCTCTC | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000776 | TCAGTTCACTCTCAT[-/TCTCTCTCTCTCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 79836 |
rs200857315 | in-del | -/GCTTTCT | 0.00949095 | 0.0682305 | intron-variant | LONRF3 | GRCh38.p7 | X:119010156 | TAATACTTGTCAAGC[-/GCTTTCT]CTGCCGTGCACAGGT | 79836 |
rs200870271 | snp | A/G | 6.96589e-05 | 0.00590124 | intron-variant | LONRF3 | GRCh38.p7 | X:119011776 | TTTTGTGTTCTGTCC[A/G]ATTGCTTTGAGATCC | 79836 |
rs201158787 | in-del | -/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974127 | TGGGTTGTGTGTGTG[-/T]GGGGGGGCTTCACGG | 79836 |
rs201264292 | in-del | -/A | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972615 | AAAAAAAAAAAAAAA[-/A]TCTAGCTCAGGTCTG | 79836 |
rs201381722 | in-del | -/C | 0.317768 | 0.24064 | intron-variant | LONRF3 | GRCh38.p7 | X:118979538 | CAAGCAATCCACTTG[-/C]CTCAGTCTCCCAAAA | 79836 |
rs201382389 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991392 | CTGTCACCACCACAG[-/A]ACTATTCTTGGGAAG | 79836 |
rs201498505 | snp | C/T | 0.00106185 | 0.0230174 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017735 | CTTCCCCACTGCCGT[C/T]GGGGGGAGTCTTCTT | 79836 |
rs201559349 | snp | C/T | 0.000352746 | 0.0132759 | intron-variant | LONRF3 | GRCh38.p7 | X:119009251 | AGAACTTTCTAAGTA[C/T]GTATATGCATATTTC | 79836 |
rs201682368 | snp | A/G | 2.73515e-05 | 0.00369798 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975335 | GTGCCTGGAACGTGG[A/G]CGGGCCGCCGACCGG | 79836 |
rs201793165 | in-del | -/CTT | 0.0199298 | 0.0978146 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975989 | GTTCCTCTGACTCTC[-/CTT]CTCCCGCTGCACTCC | 79836 |
rs201820738 | snp | A/T | 4.56971e-05 | 0.00477979 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989437 | CCCACATTGTTCTAG[A/T]CAGGAGGAAGCAGCA | 79836 |
rs202163891 | in-del | -/T | 0.375961 | 0.215949 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972962 | TCTCCTTCTTCTTCA[-/T]TTTTTTTTTTTTTCG | 79836 |
rs202239554 | snp | C/G | 2.28071e-05 | 0.00337684 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006205 | AGATCACAACGCAAA[C/G]TGTCCATTGTGCAAA | 79836 |
rs267606329 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118986987 | ACATTCTCCCGATAT[C/T]CTGAAGCTGTTGGCA | 79836 |
rs367612003 | snp | A/G | 2.29392e-05 | 0.0033866 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978452 | TGTAAGCTCCGCCCG[A/G]TGGGTTTTAAGGTGA | 79836 |
rs367843829 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004564 | TTAAAAAAAATTTCT[C/G]ATGCCTGTCCTGTAC | 79836 |
rs367926978 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019345 | TACCACAAGTATGGG[A/G]GTGTTATAATGGCAG | 79836 |
rs368038773 | snp | A/G | 2.28001e-05 | 0.00337632 | missense, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006171 | ATACTTTTTGCTTAA[A/G]ATGCCTAGAAAGATG | 79836 |
rs368114169 | snp | A/G/T | 7.18405e-05 | 0.00599299 | intron-variant | LONRF3 | GRCh38.p7 | X:119014373 | TATAGAAAAATGTCT[A/G/T]TTTTTAAACGGGTTG | 79836 |
rs368118941 | snp | A/G | 7.10985e-05 | 0.00596189 | intron-variant | LONRF3 | GRCh38.p7 | X:118978302 | TTAACACCTGCTTGC[A/G]CTGGGGGCCATTAAT | 79836 |
rs368482113 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994773 | GGTAAAAGGCCTTGT[C/T]CAACAGGAAAATATC | 79836 |
rs368497017 | in-del | -/G | 0.005278 | 0.0510994 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017741 | CACTGCCGTCGGGGG[-/G]AGTCTTCTTGTAAAT | 79836 |
rs368497969 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980736 | TCAGGGAGCTGCCTA[A/G]GAGTAAGAGGACTTG | 79836 |
rs368511479 | snp | A/C | 7.00722e-05 | 0.00591871 | intron-variant | LONRF3 | GRCh38.p7 | X:118978332 | TAAAGGTTTTTCTTT[A/C]TTATTTTGACAGCTC | 79836 |
rs368659407 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010853 | GCATGGTGGCTCATG[C/T]GTGTAATCCTAGTAT | 79836 |
rs368785677 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999239 | GTTGAAGCACTCAAA[A/G]CAAGCCTCCCATGCT | 79836 |
rs368889017 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010133 | CACTTAATTAATGGT[A/G]ATAATACTAATACTT | 79836 |
rs368940484 | snp | C/T | 0.000479479 | 0.0154761 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990525 | ACCACTTGCATCTTT[C/T]GACGCATCTGACCTT | 79836 |
rs369058353 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980647 | AGAACACATTTAGTG[A/T]TTAATACAAGTCACC | 79836 |
rs369180848 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987461 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTT]GTAGAGACGGGGTTT | 79836 |
rs369351196 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005728 | AGAATGTGTGTGCGT[G/T]TGTGTGTGTTTGTGT | 79836 |
rs369410971 | snp | A/G | 0.000438757 | 0.0148049 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017733 | ACCTTCCCCACTGCC[A/G]TCGGGGGGAGTCTTC | 79836 |
rs369418280 | snp | C/T | 9.36505e-05 | 0.00684226 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009245 | AATGGAAGAACTTTC[C/T]AAGTATGTATATGCA | 79836 |
rs369471661 | snp | A/G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984053 | TAATAGCTAACATTC[A/G/T]TTGAGAATTTCTTCT | 79836 |
rs369498035 | snp | A/G | 0.000976086 | 0.0220701 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975135 | AAAGTCCCGCAAGGC[A/G]AGGCGCTGGCGCCGG | 79836 |
rs369535074 | snp | A/C | 0.000189982 | 0.00974449 | intron-variant | LONRF3 | GRCh38.p7 | X:118989376 | ATATTAGTCCTAAGA[A/C]GATTCTGATATGTGG | 79836 |
rs369547672 | snp | A/T | 6.84236e-05 | 0.00584869 | intron-variant | LONRF3 | GRCh38.p7 | X:118982787 | TGTTAATAGGCTGAA[A/T]AAAATGGGATTGAAT | 79836 |
rs369566202 | snp | C/T | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012128 | TGTCCCTTTGGTGGT[C/T]AGTTTACCATGTGAG | 79836 |
rs369595215 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986425 | AAGCAAAATGGGTAG[C/T]GGAGAAAAGAAACAG | 79836 |
rs369621434 | snp | C/T | 2.28702e-05 | 0.00338151 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017620 | TCCCCTTCCTAGCAA[C/T]GAGGTCCTTAAAGGA | 79836 |
rs369750620 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979147 | TTGGGACTACAGGCG[C/T]CCGCCACCACACCTG | 79836 |
rs369759972 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013874 | GAGAAAACAGATGTA[A/G]AAATGAAAAGGGCAA | 79836 |
rs369785887 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003470 | CTAATACCATTTATT[A/G]AGAATGCTATTTATG | 79836 |
rs369997135 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | LONRF3 | GRCh38.p7 | X:118995199 | GAACCTTCAAAACCA[C/T]GCAAATAACATGGAA | 79836 |
rs370157712 | snp | C/T | 0.00015987 | 0.00893921 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989643 | AATCCCAAGAAGAAA[C/T]GGGGATGCCTAATAA | 79836 |
rs370189986 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006637 | CTGTCGCCCAGGCTG[G/T]AGGGCAGTGACGTGA | 79836 |
rs370231103 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979460 | CACCATGCCCGGCTA[A/T]TTTTTTGTATTTTTA | 79836 |
rs370270357 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000801 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 79836 |
rs370466412 | snp | C/T | 0.000497412 | 0.0157626 | intron-variant | LONRF3 | GRCh38.p7 | X:118978294 | TACAGGACTTAACAC[C/T]TGCTTGCGCTGGGGG | 79836 |
rs370732016 | snp | G/T | 0.000189982 | 0.00974449 | intron-variant | LONRF3 | GRCh38.p7 | X:118978322 | GGGCCATTAATAAAG[G/T]TTTTTCTTTCTTATT | 79836 |
rs370856932 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002782 | TGATGAACTTAAAAG[C/T]GCTTCTTCTTGTTTT | 79836 |
rs370895776 | snp | A/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973758 | CCCAGCAGGCCGGGT[A/G]CATCCCTGCCGCGCC | 79836 |
rs370923462 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006930 | GGTTTCACCATATTG[A/G]TCAGGCTGGTCTCGA | 79836 |
rs370939316 | snp | C/T | 2.28522e-05 | 0.00338017 | missense, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013154 | CTCCATCAGAGCCAG[C/T]GGGATGGCTACAACA | 79836 |
rs370944478 | snp | C/G | | | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989483 | AGCAGTCTGATGGAC[C/G]CAGCTAAAGTGAAGG | 79836 |
rs370968623 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995160 | AGACCACAGTGGAAT[A/T]AAACTGGAAATCAAC | 79836 |
rs371037725 | snp | C/T | 6.9033e-05 | 0.00587467 | intron-variant | LONRF3 | GRCh38.p7 | X:118990465 | TCTTGCTTTCTAAAT[C/T]GCAGATCCTCCCACT | 79836 |
rs371122942 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119015796 | TTGGCAGCAGCAGCA[A/C/T]CAGCAAAAAAGAAAA | 79836 |
rs371160667 | snp | C/G | 0.000331791 | 0.0128758 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975381 | GGGGTCAAGCTCTCC[C/G]CCTTGATGGTGGCCA | 79836 |
rs371174403 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981412 | ATCGCTTGAACCTAG[A/G]AGGTGGAGGTTGTAG | 79836 |
rs371288525 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003961 | ATTGCTGGTATATAG[A/G]ACTATAATTGTGTGT | 79836 |
rs371342500 | snp | C/G | 2.31892e-05 | 0.00340501 | intron-variant | LONRF3 | GRCh38.p7 | X:118990585 | GTGTACTATCATTTA[C/G]TTCCTGATGTTTCTT | 79836 |
rs371443437 | snp | A/C | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012383 | CTTGGAAGATTGGTG[A/C]GTTAATAATGTACAT | 79836 |
rs371529751 | in-del | -/GA | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012613 | ACAGAGAGAGAGAGA[-/GA]AAGAAGGGGGTCAAA | 79836 |
rs371622507 | in-del | -/GT | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005431 | GAAGTATATGTATGT[-/GT]ATATATATGTATGTA | 79836 |
rs371626763 | snp | C/T | 6.9185e-05 | 0.00588113 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974768 | CCTCGTCTCCTCCCG[C/T]GTCCCTCTTCCCATG | 79836 |
rs371628294 | snp | C/T | 2.42607e-05 | 0.00348278 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013226 | GCCAGTGCCAAGAAT[C/T]CCAAAGCCAGGCTAT | 79836 |
rs371699379 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011525 | CACAATATTAAGATA[A/C]TAGAGAACTTCTTCA | 79836 |
rs371807323 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016658 | CCCTGGGGCAGAATA[C/T]ATTTCTAATGTGAAT | 79836 |
rs371812668 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984632 | CTCTGGAGACCCAAA[A/G]AGGCATAAGTCACAG | 79836 |
rs371840341 | in-del | -/TA | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005430 | TGAAGTATATGTATG[-/TA]TATATATATGTATGT | 79836 |
rs371914349 | snp | C/T | 0.000356935 | 0.0133544 | intron-variant | LONRF3 | GRCh38.p7 | X:119017529 | CATTGTGTTTCTCTG[C/T]TGCAGATGAACCCGA | 79836 |
rs371959567 | snp | A/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012640 | CAAACTTGCCCTTTT[A/G]TATTAATAACAACCC | 79836 |
rs371970117 | snp | A/G | 7.14039e-05 | 0.00597468 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017704 | AGTGAGTGGATTGCC[A/G]AAGAGGAGCTCCCAC | 79836 |
rs372090669 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118977309 | ATACCTTTTAGCCAT[A/C]CCCCAGGGGCCAGGA | 79836 |
rs372228057 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999595 | GTTTTCTCTGAAAAC[C/T]AAGAATCCTGAGGTG | 79836 |
rs372320440 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119019039 | GCTACTTGGGAGGCT[C/G]AGGCAGGAGAATCAC | 79836 |
rs372522802 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000462 | ACTGGGGGAGCTCTG[A/T]TGAGAGAAGTTACCC | 79836 |
rs372583896 | snp | G/T | 2.2792e-05 | 0.00337572 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011911 | TTACCGCCTGATGAT[G/T]CGTAGATGCATTGAG | 79836 |
rs372598058 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003641 | ACTGCAGCTTTATAT[A/G]TTCTGTAATCTGGTA | 79836 |
rs372626612 | snp | A/G | 0.000320465 | 0.0126542 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017630 | AGCAATGAGGTCCTT[A/G]AAGGACAGACTGAAT | 79836 |
rs372673857 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000794 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs372734245 | snp | C/T | 0.000192114 | 0.00979898 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974929 | GCCCCGCACCTCTAC[C/T]GACGCGGGAGCCAGA | 79836 |
rs372823698 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | LONRF3 | GRCh38.p7 | X:119004568 | AAAAAATTTCTGATG[A/C]CTGTCCTGTACACTG | 79836 |
rs372886535 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118979659 | GGAAGGTGAGAGTGG[G/T]GTTGCTGCCCTGGTG | 79836 |
rs373023511 | in-del | -/CAA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995526 | TTGAAACAACAACAA[-/CAA]TACAAAAGATAAATG | 79836 |
rs373138792 | snp | A/G | 2.30622e-05 | 0.00339567 | intron-variant | LONRF3 | GRCh38.p7 | X:118982962 | AGTTGAAATGACATC[A/G]GGTCCAGCTGCCTAC | 79836 |
rs373203584 | snp | A/T | 6.86554e-05 | 0.00585858 | synonymous-codon, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006226 | ATTGTGCAAAGACGG[A/T]CTTTCACAGGTAAAT | 79836 |
rs373337693 | snp | C/T | 0.000354216 | 0.0133035 | intron-variant | LONRF3 | GRCh38.p7 | X:118989380 | TAGTCCTAAGAAGAT[C/T]CTGATATGTGGCCCT | 79836 |
rs373397719 | snp | C/T | 2.38926e-05 | 0.00345626 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017715 | TGCCGAAGAGGAGCT[C/T]CCACCTTCCCCACTG | 79836 |
rs373462476 | snp | A/G | 0.000191982 | 0.00979561 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975566 | CCAGGTGGAGGCGGC[A/G]CTGCTCAAGTACAAC | 79836 |
rs373580221 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990716 | TCACATGGGTCAGCT[C/T]GTGTCCCCTTCCCAG | 79836 |
rs373586990 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | LONRF3 | GRCh38.p7 | X:119006688 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 79836 |
rs373592030 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998969 | CTGGCCCTAAAAAAG[C/T]ATTTTCATACACTAC | 79836 |
rs373593893 | snp | A/G | 0.000171878 | 0.00926874 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012015 | GGAGGTTGTGTAATG[A/G]GGGATTTCTGTTTTA | 79836 |
rs373599029 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975061 | TGTATAGACAGCTCT[C/T]CGAGCGGCAGCAGCT | 79836 |
rs373614040 | in-del | -/TTTTTTTTTTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979008 | TCTTTCTTTTTTTTT[-/TTTTTTTTTTT]GAGACAGAGTTTCCC | 79836 |
rs373815186 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982684 | ATTAGAACAGTTGCC[C/T]GCATTTTAGGGCTGT | 79836 |
rs373946250 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998503 | GACTACAAATACGGT[A/G]CAGTGTATAATGCTC | 79836 |
rs373951965 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985876 | AACTGGAGTTTGGTG[C/T]TCTGTCAAATTTTGT | 79836 |
rs373956047 | snp | C/T | 0.000189982 | 0.00974449 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014344 | CATGCCGGAGAAAGA[C/T]GCCGATCCTCAGGTA | 79836 |
rs374301918 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010788 | GTTTTGGTTCCCCAA[C/T]GGGTTGTGTGTGTGA | 79836 |
rs374307396 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994244 | TAAAAGATACAGAAC[C/T]GCAGAATGGATAAGA | 79836 |
rs374415671 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990408 | GGATTATTTTGCCTC[A/G]GAAGTACTATCTATG | 79836 |
rs374497464 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981243 | TAATCCCAGCACTTT[G/T]GGAGGCTGAGGCAGG | 79836 |
rs374531528 | snp | A/G | 0.000420639 | 0.0144963 | intron-variant | LONRF3 | GRCh38.p7 | X:118990602 | TCCTGATGTTTCTTC[A/G]TCTCTGGTGTCTGGA | 79836 |
rs374537362 | snp | A/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973291 | GTGGCTGCAGCAGGG[A/G]GCAACAATAGGTCTT | 79836 |
rs374576989 | snp | A/C | | | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976923 | GTCTCCACGTGTTTA[A/C]TCTCCACTCAAGCTT | 79836 |
rs374596992 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119007086 | CAGGAAAATGAGGCA[A/G]CATGCAGCTTTTTAT | 79836 |
rs374597343 | snp | A/T | 5.10621e-05 | 0.00505257 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013249 | CAGGCTATCCTTGTA[A/T]CTTGATACACAAAGA | 79836 |
rs374614072 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006606 | TTGTTTTGTTTTGTT[G/T]AGACGGAGTCTCGCT | 79836 |
rs374755826 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979185 | TTTGTATTTTTTTTT[-/T]GTAGAGACAGGTTTT | 79836 |
rs374783947 | in-del | -/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974134 | GTGTGTGTGGGGGGG[-/G]CTTCACGGATACCCC | 79836 |
rs374846702 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118996900 | GCGCTCCAGCCTGGG[C/T]GACAGAGCTAGACTC | 79836 |
rs375032873 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015479 | GGCTTCTTTCCCCCC[C/G]CATGCAAAGGCATCA | 79836 |
rs375080896 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003031 | CCAGATGATCCACCC[A/G]CCTCAGCCTCAGAGT | 79836 |
rs375173882 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980408 | GTCAGGTTTTGCCAT[A/C]TAATGAATTTTGATG | 79836 |
rs375230815 | in-del | -/AGAAATAAAACACACT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983453 | TTCAGCTCCTTTGCT[-/AGAAATAAAACACACT]GCCTCACAAATGCTA | 79836 |
rs375247400 | snp | C/T | 3.09148e-05 | 0.00393147 | intron-variant | LONRF3 | GRCh38.p7 | X:118989687 | GGTACTGGCTCTACC[C/T]AGAGAGAAGGTAGCT | 79836 |
rs375251662 | snp | A/C | 0.000189982 | 0.00974449 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017607 | AGCCGAGCTCAGCTC[A/C]CCTTCCTAGCAATGA | 79836 |
rs375302904 | snp | A/G/T | 4.63868e-05 | 0.00481577 | intron-variant | LONRF3 | GRCh38.p7 | X:118990429 | ACTATCTATGAAACC[A/G/T]GGGTGGCTCCAGCGC | 79836 |
rs375345945 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016134 | CAAATAATTTCAGGT[A/G]TAGGCACTTTGACCA | 79836 |
rs375356638 | snp | G/T | 2.3245e-05 | 0.0034091 | intron-variant | LONRF3 | GRCh38.p7 | X:119011766 | TGACCAATATTTTTG[G/T]GTTCTGTCCGATTGC | 79836 |
rs375359807 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005306 | GTGAGCCTTTTTTTA[A/G]GCAAAGCAAATCCAT | 79836 |
rs375449498 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986011 | GGTTTTAGAAGCAAA[A/G]TCACCTGCTCTCCTT | 79836 |
rs375523789 | snp | C/T | 0.000139984 | 0.00836495 | intron-variant | LONRF3 | GRCh38.p7 | X:118982988 | CCTACTGGACCCTCC[C/T]CTCTCTGTCTTATCT | 79836 |
rs375533124 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985298 | CCAAGGATACTGCCT[C/T]CTCAGAACTGGCTTG | 79836 |
rs375572359 | snp | C/T | 0.000333047 | 0.0129001 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975594 | AACGAGGCAGTTAAG[C/T]TGGGTGAGTCCAACG | 79836 |
rs375596737 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988562 | CTCCCAGCTATATGC[C/T]CCCCTTTTTCACCTG | 79836 |
rs375629486 | snp | C/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014165 | ACTCTGGGAATGATG[C/G]AGAGGGTACAGAATG | 79836 |
rs375770860 | snp | A/G | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012499 | CAAAATTTATTTCTC[A/G]TGGTTCTGGAGGCTG | 79836 |
rs375779830 | snp | A/T | 0.000189982 | 0.00974449 | synonymous-codon, nc-transcript-variant, downstream-variant-500B, utr-variant-3-prime, intron-variant | LONRF3 | GRCh38.p7 | X:119013171 | GGATGGCTACAACAC[A/T]GCCGACATTGAATAC | 79836 |
rs375809050 | snp | A/C | 0.0002014 | 0.0100329 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974756 | GGTCCCTAGACGCCT[A/C]GTCTCCTCCCGTGTC | 79836 |
rs375923190 | in-del | -/TG | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974128 | GGTTGTGTGTGTGTG[-/TG]GGGGGGCTTCACGGA | 79836 |
rs375923891 | snp | C/T | 9.5109e-05 | 0.00689532 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017703 | TAGTGAGTGGATTGC[C/T]GAAGAGGAGCTCCCA | 79836 |
rs375958514 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979129 | CCTCAGCCTCCTGAG[C/T]AGTTGGGACTACAGG | 79836 |
rs375972950 | snp | A/G | 6.89861e-05 | 0.00587267 | intron-variant | LONRF3 | GRCh38.p7 | X:118990466 | CTTGCTTTCTAAATC[A/G]CAGATCCTCCCACTG | 79836 |
rs376086121 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993872 | TGGGGACCTATCTTC[A/T]GCCTCCTCAAGCAAA | 79836 |
rs376087073 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118982102 | TCTTTCCCAGAGCAG[C/T]TGGGCTTGGGCCCTG | 79836 |
rs376149642 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | LONRF3 | GRCh38.p7 | X:119000800 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 79836 |
rs376203578 | snp | A/G | 0.000108903 | 0.00737832 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974942 | ACCGACGCGGGAGCC[A/G]GAGCAAGAGCAGTCT | 79836 |
rs376253894 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011326 | TCCTTTGCAGACTCT[C/T]TGGGGTCCTTGCAAA | 79836 |
rs376265343 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980678 | AGTGTCTTAACCCAA[A/G]GGAGCTTTAGTGGGG | 79836 |
rs376427123 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006914 | TTTTTAGTAGAAATG[A/G]GGTTTCACCATATTG | 79836 |
rs376460136 | snp | C/G | 2.30094e-05 | 0.00339178 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989501 | GCTAAAGTGAAGGGG[C/G]ATGGTCAGCAGCACC | 79836 |
rs376495628 | snp | C/T | 7.10416e-05 | 0.00595951 | intron-variant | LONRF3 | GRCh38.p7 | X:118989716 | CTTGGAGGAGATCCC[C/T]GGGCTCACCAATATA | 79836 |
rs376688770 | snp | C/T | 0.000110634 | 0.00743671 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974819 | GATGCTGAGCTTGCC[C/T]GCTGAGGTCAGCAGC | 79836 |
rs376699119 | in-del | -/CT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978984 | TCTCTCTCTCTCTCT[-/CT]TTCTGTTTTCTTTCT | 79836 |
rs376884206 | snp | G/T | 0.000834695 | 0.020412 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011999 | AGCCATGCGAGCAAA[G/T]GGAGGTTGTGTAATG | 79836 |
rs376956529 | snp | G/T | 7.11221e-05 | 0.00596288 | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013207 | AGACCAAAAGGTAAG[G/T]GTGGCCAGTGCCAAG | 79836 |
rs377049062 | in-del | -/AGACTT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999468 | TGTGCGCTGTGGAGT[-/AGACTT]GACTTAGCCTGCTCA | 79836 |
rs377232773 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119017222 | AAAGGGAGAGAAAGA[C/G]GAAGGCAGAGGGCAT | 79836 |
rs377240742 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119005167 | CTGAACACTCTTGTG[A/G]GGTGAAAATAGGCTG | 79836 |
rs377244391 | snp | A/G | 2.28551e-05 | 0.00338039 | missense, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978368 | GACCACTTGCTTTAT[A/G]GCAATCGGTCTCAGA | 79836 |
rs377457379 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119006607 | TGTTTTGTTTTGTTG[A/T]GACGGAGTCTCGCTC | 79836 |
rs377579748 | snp | A/G | 4.68604e-05 | 0.00484025 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013006 | CAGAACTCATCAAGG[A/G]TCTAGTCTCTCGACT | 79836 |
rs377610734 | snp | C/T | 4.60299e-05 | 0.00479717 | intron-variant | LONRF3 | GRCh38.p7 | X:118990464 | TTCTTGCTTTCTAAA[C/T]CGCAGATCCTCCCAC | 79836 |
rs377631096 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988981 | TTTGGGGATCGCAGA[C/T]GGCCGTGAATGGCAG | 79836 |
rs377745304 | snp | A/C | 0.00738971 | 0.0603345 | intron-variant | LONRF3 | GRCh38.p7 | X:118986059 | ATATGGAAACACACA[A/C]ACACACACACACACA | 79836 |
rs377761993 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995154 | TCTCTGAGACCACAG[A/T]GGAATAAAACTGGAA | 79836 |
rs386417464 | in-del | -/AA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981484 | CAAGATTCTATCTCA[-/AA]AAAAAAAAAAAAAAA | 79836 |
rs386417465 | in-del | -/AA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981498 | AAAAAAAAAAAAAAA[-/AA]AGAGTATATGGATTG | 79836 |
rs397780964 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991873 | TAACTATTTTTTTTT[-/T]CCTTGTAGACCAGAG | 79836 |
rs397789437 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998186 | GTTTATGGCAACACA[-/A]TTCACAATTGCAAAA | 79836 |
rs397803186 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118980579 | GATTCATTTTTTTTT[-/T]CTGAGAAGGTTTTCT | 79836 |
rs397967019 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118977180 | TGGGGAAAAAAAAAA[-/A]CATCAAAGCCTGTTG | 79836 |
rs527429009 | snp | G/T | 0.000388802 | 0.0139374 | intron-variant | LONRF3 | GRCh38.p7 | X:118986899 | GTAGAAACTTAAGTA[G/T]TGAAGTCTTCTGTTT | 79836 |
rs527626565 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009873 | CTTCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 79836 |
rs529267848 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987108 | TCACCCAGCTCGCTC[A/G]TGACGCTTCGTTTGG | 79836 |
rs529549087 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118983737 | CACCCACTATTCACC[A/G]CGGAGCCTTACGGTT | 79836 |
rs529971322 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981048 | TATTTCCCAACATTT[C/G]TATGTAAAATGCCCC | 79836 |
rs530594420 | snp | A/G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988350 | AACCTTGGCTTTCCA[A/G/T]TGTCAACCAGCTGGG | 79836 |
rs530990011 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992336 | TGTTGGGGAGGGCAC[A/G]GTGGAAGTGAGACTG | 79836 |
rs531222233 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118999761 | ACTCGAAATTTAAAA[G/T]CCATCATTTCCCTTA | 79836 |
rs533130419 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119014996 | TTAGGTTCTACTGAT[C/G]AGTGTTCTTCCTGGG | 79836 |
rs535708536 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004936 | TGGAAGTTGGATAGA[C/T]TTTCATCTGTCAACA | 79836 |
rs536522926 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118985285 | TTTTGGGAGAATTCC[A/G]AGGATACTGCCTCCT | 79836 |
rs537626070 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994227 | GGCCTAAATGCCCCA[C/T]TTAAAAGATACAGAA | 79836 |
rs538131349 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007088 | GGAAAATGAGGCAAC[A/C]TGCAGCTTTTTATGC | 79836 |
rs538899409 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994045 | ATCTTGAAACAAATC[C/T]TGGAAACACAACAAA | 79836 |
rs539960151 | snp | A/G | 0.00028884 | 0.012014 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012859 | ACACGAATACATTAC[A/G]AATTTTTTTTCTTCA | 79836 |
rs541693076 | in-del | -/CCTT | 0.01368 | 0.0815649 | intron-variant | LONRF3 | GRCh38.p7 | X:118978946 | ACGTTCTCTTTCTTC[-/CCTT]CCTTCCTTCCTTCCT | 79836 |
rs542056587 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981417 | TTGAACCTAGGAGGT[A/G]GAGGTTGTAGTGAGC | 79836 |
rs542637607 | snp | C/T | 0.000353982 | 0.0132991 | intron-variant | LONRF3 | GRCh38.p7 | X:118987112 | CCAGCTCGCTCGTGA[C/T]GCTTCGTTTGGCTGT | 79836 |
rs543807292 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118979454 | GTGTGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 79836 |
rs543843451 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | LONRF3 | GRCh38.p7 | X:119015676 | GATCAGCAATGGTAA[C/T]GGGAAAACACAGATG | 79836 |
rs545415169 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995803 | AGGAAGGATGAGATA[A/C]CATGAACAGACCAAT | 79836 |
rs545968373 | snp | C/G | | | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976117 | AGGAGATGTCCGGTC[C/G]GCGCCTGCGTCCGCC | 79836 |
rs548093633 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119002800 | TTCTTCTTGTTTTTT[A/T]ATTTTTTTTTTATTT | 79836 |
rs549336807 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118999993 | TTTCCAACAGGGTTT[C/G]TCTATAAGTTAGACA | 79836 |
rs551190689 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:118992766 | AGCCTCATGGAGTCC[A/C]TTGCACCCACCACCA | 79836 |
rs551592817 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984221 | TCATGCAGCTGGTGA[C/T]TGGTGGGAAAGTATT | 79836 |
rs551964540 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992092 | GCACAAAAATTAAGA[C/T]GGTTGGCAGGCTGCT | 79836 |
rs553029193 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999034 | ATTTCCTCGCCCTTT[A/T]TGAGCACATATGCTT | 79836 |
rs553982458 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005129 | ACGAGGGAGCCGTGC[A/G]GCTGGCAGCCTCTGA | 79836 |
rs554365013 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013312 | GGCCTTGGGATTTCA[C/T]ACCAAATTGCTGCAG | 79836 |
rs555758897 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015769 | TTTTCTTAGTTCTGT[C/T]ATTATGTTGCTTTGG | 79836 |
rs557988625 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014475 | AGAGAGGAAGATGGA[C/T]TTAATTTGGTGTTGT | 79836 |
rs558176122 | snp | C/T | | | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976656 | GCAGTCCCCCATCTC[C/T]AGCTAGACTAGGGCA | 79836 |
rs558676248 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990793 | AGAGTGGGAAGGGAA[C/T]AGTCTATTCACAGGT | 79836 |
rs558959753 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000316 | ATGAATTTGTATACA[C/T]GGATTCTAGAGAGAA | 79836 |
rs559602660 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118987295 | ATTGAAAAAAAATTA[C/T]GAAACAGGGTCTCTT | 79836 |
rs560079664 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118985115 | CCTAGAGAGAGATCT[C/G]AAGTAGTAAAATGAA | 79836 |
rs562310267 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119009568 | ACAGGGGAACTTAAC[A/G]AAATGTCCAAAAGAT | 79836 |
rs562794854 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118980625 | TAGTATGGTTTTTTT[C/T]CCCCAAAGAACACAT | 79836 |
rs563663194 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986852 | GCTGGCTCCCTCCCC[A/C/G]CTTCACCCTCCTCCC | 79836 |
rs566137173 | snp | C/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009369 | TTGAAATTGGCTATG[C/G]TGAGAGTATTTACAC | 79836 |
rs567166722 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984975 | CAGATTCTTTTTCCC[C/T]CTTCTTGACCTATTT | 79836 |
rs568415811 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119000196 | AAGAAAGTGTCTGAA[A/G]CAATCTGTGGAGGTC | 79836 |
rs568472305 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015859 | GCTGCATCCCCAGTG[G/T]TCCCACAAATAAGCA | 79836 |
rs568593529 | in-del | -/TTTTG | 0.493543 | 0.0564531 | intron-variant | LONRF3 | GRCh38.p7 | X:119006569 | CCACGCTCGGCTAAT[-/TTTTG]TTTTGTTTTGTTTTG | 79836 |
rs569158321 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994147 | AAACCAAAGTACACA[C/T]GCAACAAAGAGCACA | 79836 |
rs570462277 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997971 | AAAAACTCAAAAAAC[A/C]GTAGATGCTGGCATG | 79836 |
rs571093548 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016205 | TGTGGGCAGAAAGCT[A/C]GTTTTAGGCTTAGAA | 79836 |
rs573096760 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981566 | CTTTCCAGTCTCCCA[A/G]CACTTCTCCCCTCTA | 79836 |
rs573212164 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986275 | ACATCCTCTGGGAGG[C/T]AAAGGCCAGCATAGG | 79836 |
rs574553159 | in-del | -/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972962 | CTCCTTCTTCTTCAT[-/T]TTTTTTTTTTTTTCG | 79836 |
rs575685646 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016595 | CTCGTGATCCACCCG[A/C]TGGCCTCCCAAAGTG | 79836 |
rs575934268 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118995847 | ATTGAAATGATAACT[G/T]AAAAATTGCTAACAA | 79836 |
rs575971158 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009743 | TATCTGTAGCTTGAG[A/C]ATAATTTAATAACTT | 79836 |
rs576346016 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | LONRF3 | GRCh38.p7 | X:118979249 | ACCTCATGATCCGCC[C/T]GCCTTGGCCTCCCAA | 79836 |
rs576456380 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015612 | CACGATCAAGCTTAA[C/T]GTTCCCCTTCACCTT | 79836 |
rs745330048 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999038 | CCTCGCCCTTTATGA[C/G]CACATATGCTTCTCA | 79836 |
rs745426597 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119011708 | TGTCAAAAAACAAAC[G/T]TGGTGTCTCTGCCTT | 79836 |
rs745430595 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118997116 | TAGAATTAGAAAAAA[A/T]ACAATTCTAAAATTC | 79836 |
rs745443495 | snp | C/T | 2.29019e-05 | 0.00338385 | stop-gained, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982938 | GCAAGATGTGAAGCC[C/T]AAAGAGTGAGTTGAA | 79836 |
rs745455165 | in-del | -/T | 0.000397679 | 0.0140954 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012861 | CGAATACATTACGAA[-/T]TTTTTTTTCTTCACA | 79836 |
rs745492628 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:118998499 | AAAAGACTACAAATA[C/T]GGTGCAGTGTATAAT | 79836 |
rs745526071 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981966 | GACTCAAGTGAAATG[C/T]TCTTCAAGCCAAGTT | 79836 |
rs745627958 | snp | A/G | 6.00006e-05 | 0.00547692 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975471 | AACGTGGTGCTCAGC[A/G]GCCTCCTCGGCAAGT | 79836 |
rs745651897 | snp | A/G | 0.000118796 | 0.00770609 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011994 | TGAGGAGCCATGCGA[A/G]CAAAGGGAGGTTGTG | 79836 |
rs745718767 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119006391 | AACCATCTATTTCTC[C/T]TGTCTTCTTTTTTTT | 79836 |
rs745743648 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119016545 | GTAGAGATGGGGTTT[C/T]GTCGTGTTAGCCAGG | 79836 |
rs745789382 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118974069 | GGCTCCTGGGAGAAG[A/G]CAAGGAACCCAGGCG | 79836 |
rs745796254 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990861 | TATGTCTTTTTTTTT[A/T]ATGTCTTTTTTTTGG | 79836 |
rs745867764 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000613 | CAGAACTTTTGGGGT[G/T]ACAAAGACATTTTGA | 79836 |
rs745927676 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974632 | TATTAGGCGGCGCGG[A/G]GCGGCCGGCATGGAG | 79836 |
rs745953210 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973365 | GGCTCTGAAGGCCAA[C/G]TGAGCCAGCGGCAAG | 79836 |
rs746003132 | snp | A/T | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973213 | GATCAGCTCTAACAT[A/T]TGTTCAGAAGCAAAA | 79836 |
rs746017053 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992593 | CCTACCAACCCTGGT[A/G]GTGGAAGACAAAGGG | 79836 |
rs746017318 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | LONRF3 | GRCh38.p7 | X:119000832 | CTCTCTCTCTCTCTC[C/T]CTCTCTCACTGTCAC | 79836 |
rs746047336 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988766 | TTGAAAAGGCTAGAG[A/T]CATTGTTGATTTTTT | 79836 |
rs746075758 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018277 | GTGGTTTACCATGTA[C/T]CTAGGGGGAAATAAC | 79836 |
rs746163412 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004781 | AGAACTTATCAAATT[A/G]TACACTTTACGTCTG | 79836 |
rs746194778 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118985685 | CATAACGTGGTGTTG[A/T]TCAAGATGCTATATT | 79836 |
rs746194872 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002720 | TATGTGTTGCAGATA[C/T]CTTCTCCTACTCTGG | 79836 |
rs746332931 | snp | A/C/G | 0.000455503 | 0.0150859 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975158 | GGCGCCGGCGCCCCC[A/C/G]GACGAGGGTAGCACT | 79836 |
rs746413662 | in-del | -/TG | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018529 | AAATAATTCATTTTC[-/TG]TGTGTGTAATACAGA | 79836 |
rs746436830 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant, utr-variant-5-prime | LONRF3 | GRCh38.p7 | X:118976812 | GTCTGGCGAAGCATG[C/T]CGGGGAGGAGGCAGC | 79836 |
rs746452188 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994886 | ACAGCAACACAATAA[G/T]AGTGAGGGACTTCAG | 79836 |
rs746471567 | snp | C/T | 0.000109109 | 0.00738529 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012858 | TACACGAATACATTA[C/T]GAATTTTTTTTCTTC | 79836 |
rs746475946 | snp | C/T | | | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012820 | GCACAGCACATAGTA[C/T]GTGCTCAATAAATGG | 79836 |
rs746478996 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118992273 | GCAAATAGCCTCGGT[C/G]GAGTTCTCAAGTCCC | 79836 |
rs746492158 | snp | A/G | 2.28175e-05 | 0.00337761 | missense, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982917 | CTTGATGGAAAGAAC[A/G]AGAGAGCAAGATGTG | 79836 |
rs746565841 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119011410 | CTGAGTCCACTTCTA[C/T]CATCAGCAACCTTCC | 79836 |
rs746568563 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013838 | GACTGACATACTCCT[A/G]TGTCTTTTCCAGCAA | 79836 |
rs746576525 | snp | A/G | 7.00877e-05 | 0.00591937 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013018 | AGGATCTAGTCTCTC[A/G]ACTCCATTCTCAATA | 79836 |
rs746723880 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119007317 | CTCCAAAGGCCCCAG[A/C]AGAACCTCACAGAAC | 79836 |
rs746733981 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118986972 | GGGGGATTCTCAGGA[A/G]CATTCTCCCGATATC | 79836 |
rs746737234 | snp | A/G | 2.42181e-05 | 0.00347972 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014159 | AAAGTGACTCTGGGA[A/G]TGATGGAGAGGGTAC | 79836 |
rs746748507 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118981668 | AGGCCATCAACATCC[A/G]TGTATCAGCCAAGAC | 79836 |
rs746846537 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999083 | ATTTGTATTCTGAAT[A/G]ATCGTTGTTGGATGA | 79836 |
rs746886434 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008452 | GGGTGTTTGGGAGGA[C/G]AGTAACAGTGACAAT | 79836 |
rs746901214 | snp | A/G | 0.000321595 | 0.0126765 | intron-variant | LONRF3 | GRCh38.p7 | X:118987104 | CAACTCACCCAGCTC[A/G]CTCGTGACGCTTCGT | 79836 |
rs746913708 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005474 | TATGTATATATGTGT[A/G]TATATGCATCAATAT | 79836 |
rs746933531 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986172 | AAGCTACATTAGAAC[A/G]CACGTCTACCCTCCC | 79836 |
rs746978194 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016608 | CGCTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 79836 |
rs747047671 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118990411 | TTATTTTGCCTCAGA[A/G]GTACTATCTATGAAA | 79836 |
rs747144199 | snp | G/T | 0.00105904 | 0.0229869 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974657 | ATGGAGCTCCCGGAG[G/T]CGCGGCAGGGTCAGG | 79836 |
rs747158850 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007400 | AGAGCTTTTGCAGAC[C/T]GCAGCCCTCTAGGAC | 79836 |
rs747175040 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994782 | CCTTGTCCAACAGGA[A/G]AATATCACAATCCTA | 79836 |
rs747194329 | snp | C/G | 0.000106264 | 0.00728841 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975631 | CGGGCCGGGGCTGGG[C/G]CTCGGTGGCTACATG | 79836 |
rs747217142 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015395 | CCCTCTTCCTCTTGC[A/G]TTCTGAGGTTCTAAG | 79836 |
rs747229759 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118980804 | GCTAAGGAACTTGAT[-/A]AGTGTGGTGAGAAGC | 79836 |
rs747245867 | snp | A/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118972869 | ATGTGACAAATCCAA[A/G]GCTTCAAGCCAAGTT | 79836 |
rs747257911 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119000845 | TCTCTCTCTCACTGT[A/C]ACTCTCTCTTCCTCC | 79836 |
rs747303193 | snp | A/G | 2.3788e-05 | 0.00344869 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017705 | GTGAGTGGATTGCCG[A/G]AGAGGAGCTCCCACC | 79836 |
rs747337997 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988913 | AGGTAACTTGGCAGG[C/T]CTGTGAACAGACCTG | 79836 |
rs747363223 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998230 | CCAAATGCCCATCAA[C/T]GAGTGGATAAAGAAA | 79836 |
rs747387313 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118980132 | TAAAGCTTCCTGGAT[A/G]TAGTGCTCTGTCTCT | 79836 |
rs747423161 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016449 | GCCTCCCAGGTTCAC[A/G]CCACTCTCCTGCCTC | 79836 |
rs747453241 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997581 | TTCATGACCGAGAAC[C/T]GAAAAGCAAATGCAA | 79836 |
rs747512043 | snp | G/T | 4.64199e-05 | 0.00481745 | intron-variant | LONRF3 | GRCh38.p7 | X:118990423 | AGAAGTACTATCTAT[G/T]AAACCGGGGTGGCTC | 79836 |
rs747519298 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001769 | TGTCCTTTTGTGTGT[A/G]TTTTATTCATCTGCT | 79836 |
rs747526914 | snp | A/G | 2.2876e-05 | 0.00338193 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118990547 | TCTGACCTTGAATGC[A/G]CTCTATGTATGAGGT | 79836 |
rs747552795 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118984115 | GAGTATATTATTTAA[A/G]TCCCACTACATTCCT | 79836 |
rs747557646 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009843 | GGTACGATCTTGGCT[C/T]ACTGCAACCTCCGCC | 79836 |
rs747565142 | snp | A/T | 1.75915e-05 | 0.00296571 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974964 | GAGCAGTCTCCGGGG[A/T]CCTCAACGCCGGAGA | 79836 |
rs747601028 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:119014608 | GAGAACTAAGTAAGA[C/T]AAGAGAATGGGAACA | 79836 |
rs747636905 | snp | A/G | 2.34395e-05 | 0.00342333 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119013004 | AACAGAACTCATCAA[A/G]GATCTAGTCTCTCGA | 79836 |
rs747664793 | in-del | -/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118976950 | CTTGCAACAGGTAAT[-/G]GGGGGGAGGAGGAGG | 79836 |
rs747676830 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119004890 | AATGGTTGAGAATTA[C/T]TGTTGTAATAGAAAA | 79836 |
rs747828209 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010778 | AGCTGGCTCTGTTTT[G/T]GTTCCCCAACGGGTT | 79836 |
rs747867558 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119009356 | TCATGCTAGCTGCTT[A/G]AAATTGGCTATGGTG | 79836 |
rs747873779 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999788 | CTTATCCTGCCCCTC[C/T]GTTCTAAGTGAGACT | 79836 |
rs747954306 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118992568 | CCCTGCCCCCACCCA[A/G]TGGTCCTTCCCTACC | 79836 |
rs748028772 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994652 | ATGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 79836 |
rs748101156 | snp | A/G | 2.27977e-05 | 0.00337614 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982898 | GTTTCTCTACTGTGT[A/G]TCCCTTGATGGAAAG | 79836 |
rs748103136 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119008661 | GGGAGTGGGACAGGG[A/C]AGGAAAGGTTCAGTG | 79836 |
rs748112511 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118978980 | TCCTTTCTCTCTCTC[C/T]CTCTTTCTGTTTTCT | 79836 |
rs748180743 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119005135 | GAGCCGTGCAGCTGG[A/C]AGCCTCTGACTCTCC | 79836 |
rs748213045 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118987652 | CTGCCCCTGGGCCAT[A/G]CCATTTGGGTGGGTT | 79836 |
rs748249161 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant, missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118987040 | ACGTAGAGTCAATGA[A/C]TACTGAAGTTACCAG | 79836 |
rs748270416 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119003343 | TTTCATCTTATGAAC[A/G]TTTTATTGTTCTGCT | 79836 |
rs748299954 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002575 | TATCATGGACAACAT[G/T]GCTATAAACATTGTT | 79836 |
rs748326242 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988476 | TATTGCTGTAGTGCT[G/T]GAGAAAACCCCAACT | 79836 |
rs748334311 | snp | A/T | 6.08902e-05 | 0.00551737 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975468 | GTCAACGTGGTGCTC[A/T]GCGGCCTCCTCGGCA | 79836 |
rs748361627 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118994901 | TAGTGAGGGACTTCA[A/G]TACTCCACTGACAGC | 79836 |
rs748364346 | snp | C/T | 2.75467e-05 | 0.00371114 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975340 | TGGAACGTGGGCGGG[C/T]CGCCGACCGGCGCTG | 79836 |
rs748407541 | snp | G/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975773 | GGTCTCTGAGTTTGT[G/T]CTGTTTTCACTGCTT | 79836 |
rs748434454 | snp | C/G | 3.31521e-05 | 0.00407123 | intron-variant | LONRF3 | GRCh38.p7 | X:118989710 | AGGTAGCTTGGAGGA[C/G]ATCCCCGGGCTCACC | 79836 |
rs748482789 | in-del | -/ACACACACAA | | | intron-variant | LONRF3 | GRCh38.p7 | X:118986094 | CACACACACACACAC[-/ACACACACAA]TCCTTGCTAGTACAG | 79836 |
rs748482898 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119011509 | AATTATAGCTATCAT[C/T]CACAATATTAAGATA | 79836 |
rs748492670 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990920 | TGGAGTGCAGTGGTG[C/T]GATTTCAGCTCACTG | 79836 |
rs748569482 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118989904 | TTAATATAATGGAAA[A/G]CCAAGGCATCAGGTC | 79836 |
rs748596193 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119016132 | GCCAAATAATTTCAG[G/T]TGTAGGCACTTTGAC | 79836 |
rs748623665 | snp | G/T | 2.37223e-05 | 0.00344392 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017701 | ACTAGTGAGTGGATT[G/T]CCGAAGAGGAGCTCC | 79836 |
rs748654372 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118998939 | TGCTGGGATTACAGG[C/T]GTGAGCCACTATGCC | 79836 |
rs748685269 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998818 | CAATTCAGCCTCCTG[C/T]CTGGCAAATTTTTGT | 79836 |
rs748743954 | snp | C/T | 2.27977e-05 | 0.00337614 | synonymous-codon, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006188 | TGCCTAGAAAGATGC[C/T]TAGATCACAACGCAA | 79836 |
rs748747507 | snp | A/C | 8.03181e-05 | 0.00633661 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974916 | GTGGCTGCAGAGGGC[A/C]CCGCACCTCTACCGA | 79836 |
rs748762524 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997685 | AGTCAGCAGAGTAAA[C/T]AGACAGCCCACAGAG | 79836 |
rs748775920 | in-del | -/GCTTGC | 0.00314168 | 0.0395091 | intron-variant | LONRF3 | GRCh38.p7 | X:118978296 | CAGGACTTAACACCT[-/GCTTGC]GCTGGGGGCCATTAA | 79836 |
rs748800596 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999875 | TAAGTTATAGCTGGC[C/T]TCTCACTGCTTGATG | 79836 |
rs748846802 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:118982439 | GAACGCATACCTGGG[A/C]AGGCCCTGAAAGCTG | 79836 |
rs748907230 | snp | A/G | 2.36323e-05 | 0.00343738 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989548 | AGAAGAGGAGGAGAA[A/G]TGGGATGCTACCTCT | 79836 |
rs748935932 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119008400 | TCACACCGTTAAATA[A/C]CCACTACCTAAACAT | 79836 |
rs748961098 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984711 | CCAGATGATGCAAGC[A/G]AGTGTATGCCCGTGA | 79836 |
rs748979369 | snp | G/T | 4.09475e-05 | 0.00452461 | stop-gained, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974799 | GAGTCAGTACGGATC[G/T]AACAGATGCTGAGCT | 79836 |
rs749016105 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118977679 | GGTTGATTGAGCCAG[A/C]TAATCTCTAATAGCC | 79836 |
rs749038959 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118993321 | GGAAATAGGTAGCTT[A/G]AAGAAAAAACAATAA | 79836 |
rs749040229 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119010520 | TACATTGGAACTACT[C/T]GGGGGATCTTTATCT | 79836 |
rs749041060 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119000827 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCACT | 79836 |
rs749049812 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118983773 | CCCAGTGTGGTTTGG[C/T]AGAGCAGTGGATAAA | 79836 |
rs749076984 | snp | A/G/T | 4.58167e-05 | 0.00478609 | missense, utr-variant-5-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118978447 | TAGCATGTAAGCTCC[A/G/T]CCCGATGGGTTTTAA | 79836 |
rs749137141 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119009530 | CAGGGTATTGTTGGC[A/G]AGAGTAAATTGGAGT | 79836 |
rs749146469 | in-del | -/A | 2.36768e-05 | 0.00344061 | intron-variant | LONRF3 | GRCh38.p7 | X:119014362 | GATCCTCAGGTATAG[-/A]AAAAATGTCTATTTT | 79836 |
rs749238163 | snp | G/T | 0.000127494 | 0.00798316 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118975645 | GGCTCGGTGGCTACA[G/T]GAGGGAGCGGGAGAA | 79836 |
rs749245203 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994457 | CACCCAGGCTGGAGC[A/G]CAATGGTGTGATCTC | 79836 |
rs749277044 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987952 | TTTGAAAACCAGGAA[A/G]CAGAACACAAGAGAG | 79836 |
rs749304828 | snp | C/T | 4.89824e-05 | 0.00494862 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012940 | ATAGGCAGAAGTCCC[C/T]TGAGCCACAGCATGG | 79836 |
rs749335532 | snp | A/C | 0.00158814 | 0.0281345 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018727 | TAGCCTCCATAACCC[A/C]CCTCTCCCCGGGGTT | 79836 |
rs749339717 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002026 | AAATGAGATATTTTG[A/G]TTTGGCTGCTCTGAT | 79836 |
rs749378682 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979438 | AGCTGGGATCACAGG[C/T]GTGTGCCACCATGCC | 79836 |
rs749411488 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018698 | CAGTTTAGCACATCA[C/T]AGTCATGCCCAACTA | 79836 |
rs749437498 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996673 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 79836 |
rs749454903 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119009438 | TGCACCCAGAGAGCC[-/A]GTTGTTAAACATACC | 79836 |
rs749457253 | snp | C/T | 2.28938e-05 | 0.00338325 | synonymous-codon, nc-transcript-variant, intron-variant | LONRF3 | GRCh38.p7 | X:119006139 | ATTCTATGAGCCAGT[C/T]ACAACACCTTGCGGG | 79836 |
rs749467889 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119002902 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG | 79836 |
rs749486593 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:118987190 | CCTGAGAAAGAAGAA[A/G]TTGAGTCACTAGTGG | 79836 |
rs749506555 | snp | A/C/G | 0.00105918 | 0.022993 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018057 | TGTGAAAACAAAGAT[A/C/G]CTAATAATGTTGCTG | 79836 |
rs749514095 | snp | C/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973945 | CCGCGAGTTCCTCAC[C/T]GTCCAGCGAGCGCTG | 79836 |
rs749527423 | snp | A/C | 2.36653e-05 | 0.00343978 | intron-variant | LONRF3 | GRCh38.p7 | X:119009115 | TTGTCTAATTGCCTC[A/C]CCCCATGTAGTGCTT | 79836 |
rs749587700 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013681 | AGATGACACATCTAG[A/T]TAATCCTTGGTTTTC | 79836 |
rs749602320 | in-del | -/CTC | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119002724 | TGTTGCAGATACCTT[-/CTC]CTACTCTGGCTTGCC | 79836 |
rs749605453 | in-del | -/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119007510 | GAAGACCTGAGAATC[-/T]TATCTTGTTTTCCCT | 79836 |
rs749647243 | snp | C/T | 2.33239e-05 | 0.00341488 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017665 | TTCGACGAGTCCTGG[C/T]CTTCATATCCCGAAA | 79836 |
rs749671006 | snp | A/C | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118976030 | TCTTACACCTGCTCG[A/C]ACCTTCCCAGCGAGG | 79836 |
rs749712198 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | LONRF3 | GRCh38.p7 | X:119003547 | TAAATCAAGAATCCA[C/T]GTCTGGATCTGTTTC | 79836 |
rs749715973 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996029 | ACAAAACCAGGAAAG[G/T]ACAACCAAAAAAAGA | 79836 |
rs749751992 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118981710 | AGGAGCTGGGGGAAT[A/G]CGGAAAGGTCTTCAA | 79836 |
rs749758658 | snp | A/G | 6.54986e-05 | 0.00572233 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975446 | GCAGCCGCCGCCGCC[A/G]CTGCGAGTCAACGTG | 79836 |
rs749799309 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119013456 | AGATCAACCCTGGGG[C/T]TCATTCAGCTTGGGA | 79836 |
rs749805170 | snp | A/T | 9.85003e-05 | 0.00701716 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974883 | GCGGCCCAAGTAGAC[A/T]TGGGCCCCCACCCAA | 79836 |
rs749869473 | snp | A/C/T | 4.61939e-05 | 0.00480575 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989513 | GGGGATGGTCAGCAG[A/C/T]ACCACATGAAAGACC | 79836 |
rs749876181 | snp | C/T | 2.42512e-05 | 0.0034821 | intron-variant | LONRF3 | GRCh38.p7 | X:119014387 | TATTTTTAAACGGGT[C/T]GTCCCACTAGAAGAG | 79836 |
rs749899150 | snp | A/C | | | intron-variant | LONRF3 | GRCh38.p7 | X:119015923 | CACAAGTGTTAATAC[A/C]AGCTTAAATATCTTT | 79836 |
rs749931634 | snp | A/G | | | upstream-variant-2KB | LONRF3 | GRCh38.p7 | X:118973854 | AGCGCTAGTTCTGGC[A/G]TTGGGGGTAGAGAGG | 79836 |
rs749966250 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999544 | CTCCAACATCCAGGG[A/G]ACAAGAAATCAAACA | 79836 |
rs749967346 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118979245 | CCTGACCTCATGATC[C/T]GCCCGCCTTGGCCTC | 79836 |
rs749974892 | in-del | -/A | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988761 | ATTCTTGAAAAGGCT[-/A]AGAGACATTGTTGAT | 79836 |
rs750017997 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118991465 | TGAATATTAGTGGTG[A/G]GCCTGAGATACTTAG | 79836 |
rs750024657 | snp | C/T | 0.000529661 | 0.016265 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017674 | TCCTGGCCTTCATAT[C/T]CCGAAACCAAAACTA | 79836 |
rs750041153 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118996367 | ATCAGTAAAGAGGAA[C/T]TCAGATTGTCACTGT | 79836 |
rs750047151 | snp | C/T | 0.000188715 | 0.00971194 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017542 | TGTTGCAGATGAACC[C/T]GAATGGCCCAGCCTG | 79836 |
rs750075923 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118986833 | CTGGAGTTCTGCCCT[G/T]CAAGCTGGCTCCCTC | 79836 |
rs750082223 | snp | A/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999793 | CCTGCCCCTCCGTTC[A/T]AAGTGAGACTTCAAA | 79836 |
rs750129236 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118987379 | GACTCCTGGTCTCAA[C/G]AGATCCTCCCACCTC | 79836 |
rs750154246 | snp | A/G | 2.31217e-05 | 0.00340004 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017653 | GACTGAATGGTATTC[A/G]ACGAGTCCTGGCCTT | 79836 |
rs750167588 | snp | C/T | 3.67438e-05 | 0.00428609 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975040 | GAATCCGTGAAGCCC[C/T]CGAGGTGTATAGACA | 79836 |
rs750196262 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119003006 | CCAGGCTGGTCTTGA[G/T]CTCCTCACCCCAGAT | 79836 |
rs750266360 | snp | C/G | 0.000117696 | 0.00767033 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975399 | TTGATGGTGGCCACT[C/G]GGCGGGCGCGTGGAG | 79836 |
rs750278299 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119001100 | TTTTTGTGTGAAAAT[C/T]TGGCCCTGCTCTGAT | 79836 |
rs750322199 | snp | C/T | 2.70636e-05 | 0.00367846 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989649 | AAGAAGAAACGGGGA[C/T]GCCTAATAAAGCCTC | 79836 |
rs750364488 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012126 | ATTGTCCCTTTGGTG[A/G]TTAGTTTACCATGTG | 79836 |
rs750375530 | snp | A/C | 5.83669e-05 | 0.00540186 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974895 | GACATGGGCCCCCAC[A/C]CAAAGGTGGCTGCAG | 79836 |
rs750416494 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118982123 | TTGGGCCCTGAGGAG[C/G]CATAAACTTCTTTAT | 79836 |
rs750456384 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118998742 | AGTCTCACTTTGTCA[C/T]CCGGGCTGGAGTGCA | 79836 |
rs750559416 | snp | A/G | 2.27936e-05 | 0.00337584 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982871 | AGGCAAGGTGGAGGA[A/G]GCACTAAGGGAGTTT | 79836 |
rs750597580 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | LONRF3 | GRCh38.p7 | X:119011129 | AAAAAAAAAAAAAAA[A/G]GAAAAAGAAAGACCC | 79836 |
rs750610939 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:119006743 | ACAGGCGCCCGCCAC[C/T]ACGCCTGGCTAATTT | 79836 |
rs750614862 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | LONRF3 | GRCh38.p7 | X:118998097 | AGTAGAACTGCCATT[C/T]GATCCAGCAATCCCA | 79836 |
rs750638171 | in-del | -/AA/AAA | 0.497894 | 0.0323819 | intron-variant | LONRF3 | GRCh38.p7 | X:118981483 | GCAAGATTCTATCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 79836 |
rs750778172 | snp | C/G | 0.000172656 | 0.00928967 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975408 | GCCACTGGGCGGGCG[C/G]GTGGAGCCCGGCGGG | 79836 |
rs750780063 | snp | C/T | 2.27892e-05 | 0.00337551 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119011876 | ACCGTTCCTTGTCCC[C/T]TGCACATCTTTGAGC | 79836 |
rs750851169 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118985376 | CTGTGGAGGAGGGAC[C/G]TCTGAAAGCTGGCAT | 79836 |
rs750866664 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118979423 | CTTAGCCTCCCGAGT[A/G]GCTGGGATCACAGGC | 79836 |
rs750907766 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:119004447 | TCCACACGTAACTGA[C/T]ATTTGAAGACCAATA | 79836 |
rs750938200 | snp | C/T | 2.39143e-05 | 0.00345783 | intron-variant | LONRF3 | GRCh38.p7 | X:119009267 | GTATATGCATATTTC[C/T]GTTTTGTTTCACTCA | 79836 |
rs750938601 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | LONRF3 | GRCh38.p7 | X:118993853 | CCTAAAAGCTAGAAG[G/T]GACTGGGGACCTATC | 79836 |
rs750960648 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119014473 | GCAGAGAGGAAGATG[A/G]ATTTAATTTGGTGTT | 79836 |
rs750995944 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119000259 | ATTTTAGTATGAAAT[C/T]CAGTTTCATGGTGCT | 79836 |
rs751005848 | snp | A/G | 2.32159e-05 | 0.00340696 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119014341 | TCCCATGCCGGAGAA[A/G]GACGCCGATCCTCAG | 79836 |
rs751017862 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118984389 | GGATGAACAAAGGCA[C/G]TTAGAAGAAACTTAT | 79836 |
rs751084700 | snp | A/G | 2.28475e-05 | 0.00337983 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989436 | TCCCACATTGTTCTA[A/G]TCAGGAGGAAGCAGC | 79836 |
rs751097770 | snp | C/G | 0.0240739 | 0.107039 | intron-variant | LONRF3 | GRCh38.p7 | X:119000813 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 79836 |
rs751155829 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118988290 | GAACCCAAATGCCTG[A/G]AGTGACTTCTAATTG | 79836 |
rs751174364 | snp | A/G | 7.41331e-05 | 0.00608778 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975393 | TCCGCCTTGATGGTG[A/G]CCACTGGGCGGGCGC | 79836 |
rs751174554 | snp | G/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118988242 | GATTTCAATAATTAA[G/T]ATCACTATTAAATGA | 79836 |
rs751175464 | snp | C/T | 2.80422e-05 | 0.00374437 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118975284 | GTTTCTATCAGACCC[C/T]GTGTCCTTGTCGTGT | 79836 |
rs751219885 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:119014859 | CCACAAAAACTTTTC[A/G]TGCCTCGGTCTATCT | 79836 |
rs751295997 | in-del | -/G | 0.00143823 | 0.0267778 | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017736 | TTCCCCACTGCCGTC[-/G]GGGGGAGTCTTCTTG | 79836 |
rs751307658 | in-del | -/TT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118978999 | TTTCTGTTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 79836 |
rs751337359 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118999603 | TGAAAACTAAGAATC[C/T]TGAGGTGTAAGTTCT | 79836 |
rs751366503 | snp | C/T | | | intron-variant | LONRF3 | GRCh38.p7 | X:118998226 | CAACCCAAATGCCCA[C/T]CAACGAGTGGATAAA | 79836 |
rs751401311 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118997017 | GCACATCCCATGCTC[A/T]TGGATGGGTAGAATC | 79836 |
rs751403931 | snp | A/G | 4.78801e-05 | 0.00489262 | missense, upstream-variant-2KB, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118974881 | CAGCGGCCCAAGTAG[A/G]CATGGGCCCCCACCC | 79836 |
rs751418453 | snp | C/G | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119018453 | TTTTTTCAGTTTGAA[C/G]TAAACAATATAAAAT | 79836 |
rs751510378 | snp | A/G | 2.2935e-05 | 0.00338629 | missense, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118989489 | CTGATGGACCCAGCT[A/G]AAGTGAAGGGGGATG | 79836 |
rs751535492 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118983550 | CAGCAGAATGTGGTA[A/G]TTATAAAAGAAAAAT | 79836 |
rs751552072 | snp | A/C | 2.29671e-05 | 0.00338866 | synonymous-codon, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119009161 | CAGCAAAAATGTAAT[A/C]ATGGAGGAGCTCATA | 79836 |
rs751582669 | in-del | -/TT | | | intron-variant | LONRF3 | GRCh38.p7 | X:118993362 | AAACTTTGGACACTC[-/TT]TTAAAAATGCAAAAT | 79836 |
rs751586950 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119012257 | TGCTTTCATTATCTA[A/G]TTGCAGCCTTGGAGC | 79836 |
rs751681961 | snp | A/G | 4.55882e-05 | 0.0047741 | synonymous-codon, intron-variant, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:118982856 | AGCCTTAGCCACCCT[A/G]GGCAAGGTGGAGGAG | 79836 |
rs751691662 | snp | A/G | 4.98511e-05 | 0.0049923 | intron-variant, nc-transcript-variant, utr-variant-3-prime | LONRF3 | GRCh38.p7 | X:119012923 | AACCCAGGGACAGGA[A/G]AATAGGCAGAAGTCC | 79836 |
rs751772758 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118990773 | CCTGACTTGGAAAAA[C/T]CTGGAGAGTGGGAAG | 79836 |
rs751792880 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118992170 | TGGACTAAAGAACAA[A/G]CCAGCAATCCCGAGA | 79836 |
rs751797741 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118999305 | GGAGGGGCTAAATGA[A/G]CAGGTTCCTTTCACT | 79836 |
rs751825761 | in-del | -/T | 0.0254112 | 0.109818 | intron-variant | LONRF3 | GRCh38.p7 | X:118991865 | AGTAAATGTTAACTA[-/T]TTTTTTTTCCTTGTA | 79836 |
rs751826650 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | LONRF3 | GRCh38.p7 | X:119006831 | CTGACCTCATGATCC[A/G]CCCGCCTCGGCCTCC | 79836 |
rs751926977 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | LONRF3 | GRCh38.p7 | X:119017926 | TACATAAACAGCAGA[A/G]GTGTTTAAGAGCCCA | 79836 |
rs751985211 | snp | A/G | | | intron-variant | LONRF3 | GRCh38.p7 | X:118994055 | AAATCCTGGAAACAC[A/G]ACAAAACAGAACCTC | 79836 |
rs751992128 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:118978677 | TTCAACTCATGACCT[C/T]CAGAGCAGCCTGGGC | 79836 |
rs752088144 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | LONRF3 | GRCh38.p7 | X:119016472 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGACTA | 79836 |