SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs709930 | snp | C/T | 0.404907 | 0.196224 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92064169 | TAGTCCTACAACCGA[C/T]GCATTGTTCCACTTT | 4287 |
rs761551 | snp | G/T | 0.449858 | 0.150189 | intron-variant | ATXN3 | GRCh38.p7 | 14:92080801 | TTGGCCTCCCAAACT[G/T]CTAGCATCACAGGCG | 4287 |
rs761552 | snp | A/G | 0.447728 | 0.152983 | intron-variant | ATXN3 | GRCh38.p7 | 14:92080832 | TAAGCCACCGTGCCC[A/G]TCCTATTTGCTGTAA | 4287 |
rs761553 | snp | C/G | 0.402908 | 0.197786 | intron-variant | ATXN3 | GRCh38.p7 | 14:92081081 | AAACAAAACACAACA[C/G]AACAAAAACCAATCA | 4287 |
rs872756 | snp | A/G | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92081580 | CTCTGAGTACTCCAT[A/G]TGGTGTGCAATCCCA | 4287 |
rs910369 | snp | A/C | 0.409891 | 0.192184 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92063938 | CATGATGTGAGCCAA[A/C]TTACCTACAAGACAG | 4287 |
rs978219 | snp | A/T | 0.206642 | 0.246211 | intron-variant | ATXN3 | GRCh38.p7 | 14:92091633 | CTTGTATTTACATTT[A/T]AAAAAAAACAGATTT | 4287 |
rs978220 | snp | G/T | 0.445328 | 0.156035 | intron-variant | ATXN3 | GRCh38.p7 | 14:92091791 | caggcttgacctctg[G/T]gctccctcctcagcc | 4287 |
rs1047795 | snp | C/T | 0.420574 | 0.182769 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92058801 | CAAAAAGCATTGTTG[C/T]TTGGCCATGATACAA | 4287 |
rs1048755 | snp | A/G | 0.395515 | 0.203286 | ATXN3 | 14 | allele_origin=G(germline)/A(germline) | 14:92082441 | ACAGACCTGGAACGA[A/G]TGTTAGAAGCAAATG | 4287 |
rs1055996 | snp | C/T | 0.365439 | 0.221752 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92061055 | CTGAATTTTTGATAC[C/T]ATTTTTAAAATCATG | 4287 |
rs1072957 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92085728 | GAAACACTTTTTGGA[C/T]TTCCAAGTGGAGATG | 4287 |
rs1072958 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92085718 | TGTTCAGTTTGAAAC[A/G]CTTTTTGGATTTCCA | 4287 |
rs1107115 | snp | A/G | 0.384785 | 0.210554 | intron-variant | ATXN3 | GRCh38.p7 | 14:92080200 | TAGCATCAGGGGAAT[A/G]GATGCAAACCATAAA | 4287 |
rs1118322 | snp | C/T | 0.445328 | 0.156035 | intron-variant | ATXN3 | GRCh38.p7 | 14:92091862 | AGCCAATTTTTTTTT[C/T]TTTCATTTTTTTTTT | 4287 |
rs1134377 | snp | A/G | 0.43088 | 0.172575 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92060820 | GCTTGAACCCTGGCG[A/G]CAGAGGATGCAGTGA | 4287 |
rs1134378 | snp | A/G | 0.431473 | 0.171952 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92060801 | AGGATGCAGTGAGCC[A/G]AGATGGTGCCACTGT | 4287 |
rs1804683 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92064166 | GTGGAACAATGCGTC[G/T]GTTGTAGGACTAAAT | 4287 |
rs1884774 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92090191 | CACTGCAGCCTCGAA[C/T]ACCTGGGCTTAAGTG | 4287 |
rs1956415 | snp | C/T | 0.422158 | 0.181278 | intron-variant | ATXN3 | GRCh38.p7 | 14:92105187 | AGCACTTCGAGAGGC[C/T]GAGGTGGGAGAATCA | 4287 |
rs1956416 | snp | C/T | 0.395453 | 0.203331 | intron-variant | ATXN3 | GRCh38.p7 | 14:92105635 | TATGAAACATGATAC[C/T]ATGTGCCAAAGCTGT | 4287 |
rs1956417 | snp | C/T | 0.396727 | 0.202413 | intron-variant | ATXN3 | GRCh38.p7 | 14:92105717 | AACGAGGAGTTTCTT[C/T]ACATATCACAAACAG | 4287 |
rs1997917 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92093424 | TTAAGATTATATTTA[C/T]AGTTAAGTGTCACTG | 4287 |
rs1997918 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ATXN3 | GRCh38.p7 | 14:92093441 | GTTAAGTGTCACTGA[C/T]GTTTTTAAAAGATCA | 4287 |
rs1997919 | snp | C/T | 0.445328 | 0.156035 | intron-variant | ATXN3 | GRCh38.p7 | 14:92093518 | CAAGATGGCCTCATG[C/T]ACCACTTATGGGGTC | 4287 |
rs1997920 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92093664 | AAAAGTATTCAAAAT[A/G]TATTTCTCTTCTTTA | 4287 |
rs2003721 | snp | C/T | 0.448195 | 0.152377 | intron-variant | ATXN3 | GRCh38.p7 | 14:92079800 | TGGAGTGCAATGGCG[C/T]TATCTCAGCTCACTG | 4287 |
rs2003722 | snp | C/G | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92079854 | GCGATTCTCCTGTCT[C/G]AGCCTCCCAAGTAGC | 4287 |
rs2006047 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | ATXN3 | GRCh38.p7 | 14:92068664 | GGTGCAATCTCAGCT[C/T]ACTGCAACCTTCGCT | 4287 |
rs2145127 | snp | A/G | 0.34989 | 0.229177 | intron-variant | ATXN3 | GRCh38.p7 | 14:92100956 | AGTTTGGAGTTTACA[A/G]ACTATGGTCACCATA | 4287 |
rs2145128 | snp | C/T | 0.151001 | 0.229563 | intron-variant | ATXN3 | GRCh38.p7 | 14:92101094 | CAAAGAAAAACTGTA[C/T]TGCTACAGGAAATAT | 4287 |
rs2145129 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ATXN3 | GRCh38.p7 | 14:92101145 | TGATTTAATGGAAGG[A/G]AAGGACAAACTGTTC | 4287 |
rs2268007 | snp | C/T | 0.00103274 | 0.0227003 | intron-variant | ATXN3 | GRCh38.p7 | 14:92083544 | AGGGCCCTACTAATA[C/T]AGTACTTGACTGAGC | 4287 |
rs2295175 | snp | A/C | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92082037 | ACCCACAAAGATTAA[A/C]ACCACAATTTACTAT | 4287 |
rs2295176 | snp | A/G | 0.438806 | 0.163867 | intron-variant | ATXN3 | GRCh38.p7 | 14:92082114 | ATATAACTACTCCTA[A/G]TAAAATATAGGTTGT | 4287 |
rs2295177 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATXN3 | GRCh38.p7 | 14:92082122 | ACTCCTAATAAAATA[C/T]AGGTTGTAAAAAGTG | 4287 |
rs2402090 | snp | A/T | 0.441705 | 0.160466 | intron-variant | ATXN3 | GRCh38.p7 | 14:92080052 | cTTTTATTTTTCTTT[A/T]AAAAAAAAAAGTGGG | 4287 |
rs2402103 | snp | A/G | 0.428182 | 0.17536 | intron-variant | ATXN3 | GRCh38.p7 | 14:92086884 | GAACATCTTGAGTAG[A/G]TGAGAAGAGCTGGGA | 4287 |
rs2402104 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087068 | TGTAACGGAAAGCCA[C/T]AAGGAAGGTGTGTAA | 4287 |
rs2402105 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087118 | AGGTTTAAAGACATA[A/G]GCTGTGAAATTAGTC | 4287 |
rs2402106 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087167 | TTATTTTTTATAAAC[A/T]TCTTGGAGAGTGGTA | 4287 |
rs2402107 | snp | C/T | | | intron-variant | ATXN3 | GRCh38.p7 | 14:92090047 | gaccagcctgggctg[C/T]aacatagtgagaccc | 4287 |
rs2402108 | snp | A/G | 0.348574 | 0.229746 | intron-variant | ATXN3 | GRCh38.p7 | 14:92093967 | TTTTTTTTTTGTGAC[A/G]GAGTCTTGCTCTGTC | 4287 |
rs2402109 | snp | C/T | 0.145642 | 0.227177 | intron-variant | ATXN3 | GRCh38.p7 | 14:92100459 | GGATAGCTGGGATCA[C/T]AGTAGAATGGAAATT | 4287 |
rs2402110 | snp | A/G | 0.399611 | 0.200291 | intron-variant | ATXN3 | GRCh38.p7 | 14:92100639 | gtatatacactgtac[A/G]cttccagtcacaaaa | 4287 |
rs2896195 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087179 | AACTTCTTGGAGAGT[A/G]GTACATAATTTTTTA | 4287 |
rs2896196 | snp | C/G | 0.314301 | 0.241589 | upstream-variant-2KB | ATXN3 | GRCh38.p7 | 14:92107649 | AGGTAGCAGCGGTTT[C/G]ATGAAACTTAAATGG | 4287 |
rs3031725 | in-del | -/GCT | | | intron-variant | ATXN3 | GRCh38.p7 | 14:92090043 | ttgagaccagcctgg[-/GCT]gtaacatagtgagac | 4287 |
rs3092822 | snp | A/C | 0.477764 | 0.10307 | intron-variant | ATXN3 | GRCh38.p7 | 14:92070819 | TTAATCATATTAAGA[A/C]TCTTAAGTAAATTTG | 4287 |
rs3178662 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92060870 | TGGCAGGTGCCTGTA[A/G]TCCCAGCTACCTGGG | 4287 |
rs3814834 | snp | C/T | 0.216982 | 0.24781 | utr-variant-5-prime, nc-transcript-variant | ATXN3 | GRCh38.p7 | 14:92106583 | GAGGGGGTGGTTCGG[C/T]GTGGGGGCCGTTGGC | 4287 |
rs3819779 | snp | C/G | 0.434687 | 0.168495 | intron-variant | ATXN3 | GRCh38.p7 | 14:92075435 | GCCTCCGAAAGTGCT[C/G]GGATTACAAGCGTGA | 4287 |
rs3819780 | snp | C/T | 0.422787 | 0.180679 | intron-variant | ATXN3 | GRCh38.p7 | 14:92075806 | TACTAATGAGCTCTA[C/T]AAGGTTTTGAATGCA | 4287 |
rs4410011 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087240 | GAAAACATAGTAGAA[A/G]TATCAGACAGCACTA | 4287 |
rs4420459 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92090215 | TTAAGTGATTCTCTC[A/G]CTTCATCCTCCCAAG | 4287 |
rs4900095 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92090694 | ACGTAATTCAAAATG[C/T]GAAAATGCAATTTTG | 4287 |
rs4904833 | snp | A/G | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92069317 | ctcaggtgatccatc[A/G]gccttggcctcccaa | 4287 |
rs4904834 | snp | C/G | 0.493402 | 0.0570581 | intron-variant | ATXN3 | GRCh38.p7 | 14:92093334 | CTAAAAAAGAAAACA[C/G]ACAATATTAACTTGA | 4287 |
rs4904835 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92094183 | CTGACCTTGTGATCC[A/G]CCCGCCTGGGCCTCC | 4287 |
rs4904836 | snp | C/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92094191 | gtgatccacccgcct[C/G]ggcctcccaaagtac | 4287 |
rs5810570 | in-del | -/C | 0.45445 | 0.218788 | intron-variant | ATXN3 | GRCh38.p7 | 14:92086824 | ATATTACAAAAAAAG[-/C]GGGGGGGGAACTGAT | 4287 |
rs5810571 | in-del | -/TGT | 0.445064 | 0.156365 | intron-variant | ATXN3 | GRCh38.p7 | 14:92090045 | GAGACCAGCCTGGGC[-/TGT]AACATAGTGAGACCC | 4287 |
rs5810572 | in-del | -/T | 0.445328 | 0.156035 | intron-variant | ATXN3 | GRCh38.p7 | 14:92091707 | TGTATAATTTGAAAC[-/T]TTTTTTTTGAGACAG | 4287 |
rs5810573 | in-del | -/T | 0.423726 | 0.179776 | intron-variant | ATXN3 | GRCh38.p7 | 14:92091852 | ACCACGCCTAGCCAA[-/T]TTTTTTTTTCTTTCA | 4287 |
rs5810574 | snp | A/T | | | intron-variant | ATXN3 | GRCh38.p7 | 14:92096641 | aaaaaaaaaaaaaaa[A/T]gaaaTGTGACTTAGT | 4287 |
rs5810575 | in-del | -/T | 0.34989 | 0.229177 | intron-variant | ATXN3 | GRCh38.p7 | 14:92101035 | TCTCTCTATAAAAAA[-/T]AGCTTTAAATTATGA | 4287 |
rs6575227 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | ATXN3 | GRCh38.p7 | 14:92075038 | ACACAGCTGATGTAG[C/T]AGAGTTTTGCTTGGG | 4287 |
rs6575228 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | ATXN3 | GRCh38.p7 | 14:92095051 | ATAAAAGAATCTTGC[A/G]AGTACATATATATAT | 4287 |
rs7142326 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | ATXN3 | GRCh38.p7 | 14:92068397 | ttttatcttgctagg[C/T]tgcctcttttggcta | 4287 |
rs7142850 | snp | A/G | 0.421526 | 0.181876 | intron-variant | ATXN3 | GRCh38.p7 | 14:92101747 | cctgtagtcccaggt[A/G]ctcaggaggctaagg | 4287 |
rs7143616 | snp | A/C | 0.431473 | 0.171952 | intron-variant | ATXN3 | GRCh38.p7 | 14:92065114 | tattcccacccacct[A/C]tcttttacccacttt | 4287 |
rs7143765 | snp | A/C | 0.431473 | 0.171952 | intron-variant | ATXN3 | GRCh38.p7 | 14:92065143 | ttctctaactagtgg[A/C]aaccactaatatgtt | 4287 |
rs7143907 | snp | C/G | 0.431473 | 0.171952 | intron-variant | ATXN3 | GRCh38.p7 | 14:92065130 | tcttttacccacttt[C/G]tctaactagtggaaa | 4287 |
rs7144492 | snp | A/G | 0.491104 | 0.0660973 | intron-variant | ATXN3 | GRCh38.p7 | 14:92072609 | agggatactcaatct[A/G]tatttcaTATATGTA | 4287 |
rs7146985 | snp | A/G | 0.438806 | 0.163867 | intron-variant | ATXN3 | GRCh38.p7 | 14:92069172 | caatctccgcctccc[A/G]ggttcaagtgattct | 4287 |
rs7148184 | snp | A/G | 0.439085 | 0.163545 | intron-variant | ATXN3 | GRCh38.p7 | 14:92078227 | gacctcaggtgatcc[A/G]cccacctcagccttc | 4287 |
rs7148258 | snp | C/T | 0.448195 | 0.152377 | intron-variant | ATXN3 | GRCh38.p7 | 14:92078434 | atggcacgatctcgg[C/T]tcaccgcaacctcgc | 4287 |
rs7149105 | snp | C/T | 0.438806 | 0.163867 | intron-variant | ATXN3 | GRCh38.p7 | 14:92072948 | AGCCAGAATACTGAC[C/T]TGTGTGTAGGTGTAA | 4287 |
rs7149601 | snp | G/T | 0.448195 | 0.152377 | intron-variant | ATXN3 | GRCh38.p7 | 14:92073104 | CACTCCATGCCCTCT[G/T]CCCCTCCACTCAAGA | 4287 |
rs7149662 | snp | C/G | 0.399432 | 0.200425 | intron-variant | ATXN3 | GRCh38.p7 | 14:92103364 | AATATTTACAGAAAA[C/G]TTGTTTACTTTAGAT | 4287 |
rs7149775 | snp | G/T | 0.439502 | 0.163061 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087578 | ggacaaggccaagat[G/T]tggtttaaccagggt | 4287 |
rs7150333 | snp | C/T | 0.49823 | 0.0296997 | intron-variant | ATXN3 | GRCh38.p7 | 14:92065669 | ggcggatcacgaggt[C/T]aggagatggagacca | 4287 |
rs7150414 | snp | C/T | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92072923 | TGCAATTTCTCCCTG[C/T]TGGTCTCTGAGCCAG | 4287 |
rs7150654 | snp | C/T | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92073083 | AATTCCTGGCACATC[C/T]GCTATCACTCCATGC | 4287 |
rs7151555 | snp | C/T | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92075424 | CGCCTGCCTTGGCCT[C/T]CGAAAGTGCTGGGAT | 4287 |
rs7152876 | snp | C/T | 0.439085 | 0.163545 | intron-variant | ATXN3 | GRCh38.p7 | 14:92075508 | ACTATGATTACTTTA[C/T]GCATTTATGCAATTA | 4287 |
rs7153193 | snp | A/C | 0.448323 | 0.15221 | intron-variant | ATXN3 | GRCh38.p7 | 14:92070350 | tttgggaggccgagg[A/C]gggcggatcatgagg | 4287 |
rs7153366 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ATXN3 | GRCh38.p7 | 14:92100412 | atagcattactattt[C/G]taatggaccccaaac | 4287 |
rs7153374 | snp | C/T | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92070423 | tctctactaaaaata[C/T]aaaaaattagccagg | 4287 |
rs7153603 | snp | C/T | 0.448195 | 0.152377 | intron-variant | ATXN3 | GRCh38.p7 | 14:92070572 | tgacagagcaagact[C/T]catctcaaaaaaaga | 4287 |
rs7153615 | snp | C/T | 0.448195 | 0.152377 | intron-variant | ATXN3 | GRCh38.p7 | 14:92070595 | aaaaaagaaaaaTAT[C/T]CATGATGTCTAAGGA | 4287 |
rs7153696 | snp | A/G | 0.448066 | 0.152544 | intron-variant | ATXN3 | GRCh38.p7 | 14:92070452 | ggcgatgtggcgggc[A/G]cctgtagtcccagct | 4287 |
rs7154147 | snp | C/T | 0.317933 | 0.240593 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087733 | aggaaatgCTTGGGC[C/T]CCAcagtagggttta | 4287 |
rs7154396 | snp | A/G | 0.428182 | 0.17536 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087954 | GATAAAAGTAGTTGA[A/G]GTAGAGAAAAAGACA | 4287 |
rs7154758 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92088091 | tttttttttttgaga[C/T]ggagtctcgctctgt | 4287 |
rs7154952 | snp | C/G | 0.44546 | 0.155869 | intron-variant | ATXN3 | GRCh38.p7 | 14:92088202 | gcctcccgagtagct[C/G]ggactacaggcgtcc | 4287 |
rs7155310 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92088424 | gaaGAACAGTGGCCT[A/G]GAAGAGGCAAAGAAG | 4287 |
rs7155635 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92088377 | gcccagccGTTAGGG[A/G]CATGTATTTCAAAGA | 4287 |
rs7155871 | snp | C/T | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92087950 | GAATGATAAAAGTAG[C/T]TGAAGTAGAGAAAAA | 4287 |
rs7157769 | snp | A/C | 0.445196 | 0.1562 | intron-variant | ATXN3 | GRCh38.p7 | 14:92092135 | catagccttctcgtc[A/C]ccaggcaaccgctgg | 4287 |