SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1349518 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186844441 | CTTTTCTTAGAATAC[A/G]TAAATGTTTTCCTAC | 151112 |
rs1451556 | snp | C/T | 0.234109 | 0.249494 | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186849535 | CCTGTGATGATTCAT[C/T]ATCTTTAACAGAAAG | 151112 |
rs1451557 | snp | C/G | 0.327445 | 0.237702 | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186850343 | ATGATGGTAATGGCA[C/G]CTTTCACAGGTGAGA | 151112 |
rs1451558 | snp | C/T | 0.455858 | 0.141853 | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186850731 | CTCTCTCTTTATATA[C/T]ATGTGTGTACATATA | 151112 |
rs1901342 | snp | C/G | 0.483852 | 0.0883933 | | | GRCh38.p7 | 2:186846094 | AATTTATGATCAAGT[C/G]TTCATAAGAAAATGC | 151112 |
rs2084752 | snp | A/C | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186845997 | actcaagatggatta[A/C]agacctaaatgtgag | 151112 |
rs2084753 | snp | A/G | 0.24932 | 0.249999 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186846029 | ccttaaactacaaaa[A/G]ctcttgaagaaaaac | 151112 |
rs2084754 | snp | A/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186846081 | ggcctgggcaaagaa[A/T]ttatgatcaagtctt | 151112 |
rs2122870 | snp | A/C | 0.32768 | 0.237625 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186842614 | CAATACATACGATTC[A/C]ATTTATAAAAAGCAC | 151112 |
rs2167395 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186842403 | TTTAAATACAAGACA[C/T]AAAAAATCTTTATTT | 151112 |
rs3100021 | snp | A/C | 0.418974 | 0.184249 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186848669 | GAACACATGTAATGC[A/C]AACCAGGTATTCATA | 151112 |
rs3100024 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186840109 | CAATACAGAAATCGC[A/G]GTTCCCTGTCAGATG | 151112 |
rs3100036 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186842637 | AAAagcacctagcag[A/G]gctcctagctaatat | 151112 |
rs3100041 | snp | C/T | 0.482979 | 0.0906686 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186847078 | ttattgggtacaatg[C/T]tcactattggggtga | 151112 |
rs3114920 | snp | C/G | | | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186849804 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 151112 |
rs3114949 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186840139 | GTTATGGCAAGTGGA[C/T]TGTGGGAGGGCATCA | 151112 |
rs3114950 | snp | G/T | 0.493793 | 0.055364 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186846295 | caacaggaaaaaacc[G/T]aataacctcattaaa | 151112 |
rs3114951 | snp | C/T | 0.418974 | 0.184249 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186848685 | AACCAGGTATTCATA[C/T]GCCTCTGACATTTTC | 151112 |
rs6434197 | snp | C/T | 0.207488 | 0.246359 | missense, intron-variant, nc-transcript-variant | ZSWIM2 | GRCh38.p7 | 2:186833980 | TGGGAAAGATGGCAG[C/T]AGCTATCAAAACATT | 151112 |
rs6708289 | snp | C/T | 0.287346 | 0.247195 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186834517 | ccctattgtgaactg[C/T]gcacatgagagatct | 151112 |
rs6711860 | snp | C/T | 0.249603 | 0.25 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186834937 | catacaagttctggg[C/T]gtaaggatgtggacg | 151112 |
rs6725956 | snp | C/G | 0.183344 | 0.24095 | utr-variant-5-prime, nc-transcript-variant | ZSWIM2 | GRCh38.p7 | 2:186849139 | GAAGCATGCTGGGTG[C/G]GGGCGGAGGCGGCCC | 151112 |
rs6726153 | snp | A/G | 0.24932 | 0.249999 | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186849195 | GCCGGTCTCCAAGAC[A/G]ACGGCGTGCAGGCTG | 151112 |
rs6736846 | snp | C/T | 0.287606 | 0.247155 | downstream-variant-500B | ZSWIM2 | GRCh38.p7 | 2:186827130 | TTAAATGCAAATTCT[C/T]TTCAAAGAATTTTGC | 151112 |
rs6744956 | snp | C/G | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186829196 | AATTAGCCATTTTAA[C/G]TAAGGATGACTCTAA | 151112 |
rs6745065 | snp | C/G | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186829246 | TGTTTGTTTACTGAA[C/G]CAACTTCATTTCAGA | 151112 |
rs6745572 | snp | C/T | 0.20964 | 0.246721 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186829683 | CTTCATTTGTGAAAA[C/T]TGACCCTACAGGGAA | 151112 |
rs6745642 | snp | A/G | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186829570 | GAAAGCTGCCTTCTC[A/G]ATAGTCTCTGTGGTA | 151112 |
rs6750068 | snp | A/T | 0.327211 | 0.237778 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186847997 | AATTAACAAATTAGG[A/T]TGGTTTTAAAGTGAC | 151112 |
rs6752200 | snp | A/T | 0.290897 | 0.248368 | downstream-variant-500B | ZSWIM2 | GRCh38.p7 | 2:186827251 | TAATAAAAATCAATA[A/T]AGCATCAATAATTTT | 151112 |
rs6757716 | snp | A/G | 0.315758 | 0.241197 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186832418 | tgagccacagcgccc[A/G]gccTAAATTTTCTGT | 151112 |
rs6760362 | snp | C/T | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186829326 | GATCAAGTAGTATTA[C/T]GCTGATTCTAATGAG | 151112 |
rs7559533 | snp | A/G | 0.385063 | 0.210376 | synonymous-codon, intron-variant, nc-transcript-variant | ZSWIM2 | GRCh38.p7 | 2:186834024 | ATATTCTATGCATTC[A/G]GTACACCTAAAAATA | 151112 |
rs7579732 | snp | C/T | | | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186846812 | ACACACACACACACA[C/T]ATAtatatatatata | 151112 |
rs7581809 | snp | A/G | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186838665 | CATATATATACACAC[A/G]CATATATATGTTGCT | 151112 |
rs7600876 | snp | G/T | 0.0410537 | 0.137264 | utr-variant-3-prime | ZSWIM2 | GRCh38.p7 | 2:186827558 | GTTTTTTAAGGTTTT[G/T]TTTTATAGGTTTGTG | 151112 |
rs7609183 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186833310 | AAATTAGTTGGTTGC[A/G]TATCAATAATGTGAA | 151112 |
rs9288136 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186846186 | aaacaatcaacagag[C/T]gaacagacaacctaa | 151112 |
rs10164815 | snp | A/G | 0.240315 | 0.249812 | missense, utr-variant-3-prime | ZSWIM2 | GRCh38.p7 | 2:186833156 | GACATCTTTTCTTCA[A/G]TCTCATTTTTAGTAT | 151112 |
rs10165106 | snp | A/G | 0.289942 | 0.246789 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186833395 | CAAATTATTAGTCTC[A/G]TATTGTATTGCATAG | 151112 |
rs10166117 | snp | C/T | 0.233818 | 0.249476 | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186851163 | GGAGAATTAAATATC[C/T]TCCTTCAGGTATATT | 151112 |
rs10166171 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186842156 | ATCTCTGAATGATGT[G/T]CAAAACATTCCTCTT | 151112 |
rs10169570 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186843066 | aatattttgatgtac[C/T]ggcttaagttaaaat | 151112 |
rs10169582 | snp | C/T | 0.234982 | 0.249549 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186843115 | cctgtttctttttac[C/T]tcttataatatggct | 151112 |
rs10169671 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186843164 | tatgttatatttcca[C/T]tggacagcCTCAGTA | 151112 |
rs10172225 | snp | C/T | 0.208016 | 0.246627 | synonymous-codon | ZSWIM2 | GRCh38.p7 | 2:186828377 | TATTTTCCCAAATGA[C/T]ACAGTGGGTAAATCT | 151112 |
rs10175178 | snp | C/T | 0.288127 | 0.247076 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186828989 | ACTGATTTCCATTTT[C/T]GATATTAAAATGCAA | 151112 |
rs10178860 | snp | G/T | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830253 | cgggcatggtggcag[G/T]tgcctgtaatcacag | 151112 |
rs10179175 | snp | C/T | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830657 | GAAATTTGTTTTCAT[C/T]TGGGGTATATTCTTA | 151112 |
rs10179285 | snp | C/G | 0.490287 | 0.0690083 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830799 | CTATTTGATGCCACT[C/G]CAACTGGTAAAACAG | 151112 |
rs10179296 | snp | C/T | 0.490231 | 0.0692021 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830843 | TAAGAGAAAAAAAAG[C/T]TTGGTTAAAAGGTCA | 151112 |
rs10181270 | snp | A/G | 0.261884 | 0.249717 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186836293 | CCTGGAATCCTCTTT[A/G]ACCAACATTCCTGAA | 151112 |
rs10183672 | snp | A/T | 0.24932 | 0.249999 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186843876 | ACACTAATGGTAATT[A/T]ATTATCTGGTATAAT | 151112 |
rs10187599 | snp | A/G | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186837883 | GCTTAACACAAAGGA[A/G]AATAATAATTATTAT | 151112 |
rs10188450 | snp | C/T | 0.287346 | 0.247195 | intron-variant, downstream-variant-500B | ZSWIM2 | GRCh38.p7 | 2:186832915 | CCACAAGCCACATAG[C/T]CAATGTGTAGTTGAA | 151112 |
rs10188850 | snp | C/T | 0.231555 | 0.249319 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186833269 | GTTACTTTGCAAAGT[C/T]GTGGATATTTTCATT | 151112 |
rs10188869 | snp | C/T | 0.287346 | 0.247195 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186833326 | TATCAATAATGTGAA[C/T]AATACACAATATTTT | 151112 |
rs10189037 | snp | G/T | 0.287346 | 0.247195 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186833292 | TTTTCATTTTGTGGA[G/T]AAAAATTAGTTGGTT | 151112 |
rs10191094 | snp | C/T | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830106 | GTTTTTggctgagca[C/T]gatggctcacgcctg | 151112 |
rs10191209 | snp | C/T | 0.287867 | 0.247116 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830225 | tctctaataaaaata[C/T]agaaaaattagccgg | 151112 |
rs10195632 | snp | A/T | 0.207586 | 0.246376 | missense | ZSWIM2 | GRCh38.p7 | 2:186828276 | CTTAGACTAGTGTGA[A/T]ATTTTCCACTGATGC | 151112 |
rs10195758 | snp | A/T | 0.206914 | 0.246259 | missense | ZSWIM2 | GRCh38.p7 | 2:186828428 | TTGGCTAATTTTATA[A/T]TCATAGGTTAATTTT | 151112 |
rs10196724 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186837003 | GCTTGGAAACCTATG[C/T]AGGCTAAAGCCACCT | 151112 |
rs10200056 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186838088 | AAAAGTTTTGTTAAA[C/T]TATCAGAAGAAAAAA | 151112 |
rs10200250 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186838268 | AGTAGACAGCTGATC[C/T]GAGGTCTAACAAAAC | 151112 |
rs10201183 | snp | C/T | 0.249603 | 0.25 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186842370 | GGATTTTCTCAATGC[C/T]TACTAATTAAAATTT | 151112 |
rs10201512 | snp | A/C | 0.234401 | 0.249513 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186842713 | TGTTGAATATGGTAG[A/C]CATTAGCCACAGGTA | 151112 |
rs10202588 | snp | A/G | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186830655 | AGGAAATTTGTTTTC[A/G]TCTGGGGTATATTCT | 151112 |
rs10203986 | snp | C/T | 0 | 0 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186848789 | TAATAAATACTATTT[C/T]CTTCTGTAATTTCAC | 151112 |
rs10204903 | snp | A/G | 0.262159 | 0.249704 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186836564 | AATTAGATTGGGCTC[A/G]TCATAATGTAATTCA | 151112 |
rs10207244 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186840582 | CCAATAACTGTTAAC[C/T]GAGATAACTGGGTGG | 151112 |
rs10207487 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186843992 | AGAAAAAATTTAAAA[C/T]TAATTATCACTTTAA | 151112 |
rs10210233 | snp | C/T | 0.248755 | 0.249997 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186841280 | TTCTTTCCAAAATTA[C/T]AGAAATATTACTAAC | 151112 |
rs10210806 | snp | A/G | 0.25045 | 0.25 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186837872 | AATGAATATAGGCTT[A/G]ACACAAAGGAGAATA | 151112 |
rs10211050 | snp | A/C | 0.23512 | 0.250668 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186838156 | TGTCCAAATTTTTCA[A/C]GTCCAACTTTATAGT | 151112 |
rs11885224 | snp | G/T | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186847921 | AGGTTGAATAGATTC[G/T]ACTGGAGAATCTTAA | 151112 |
rs11892669 | snp | A/G | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186844826 | AAAAGACATTTAAAA[A/G]TATTTAGAATAGAAA | 151112 |
rs11896398 | snp | A/G | 0 | 0 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186834668 | tgccaaaatgtttga[A/G]gactgctgttctaga | 151112 |
rs11898665 | snp | C/T | 0.287346 | 0.247195 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186832147 | TGAGATGGAGTCTCA[C/T]TCTGTTGCCTCGGTT | 151112 |
rs11898741 | snp | C/T | 0.287346 | 0.247195 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186832347 | GGCTGGTCTCGAACT[C/T]CTGACCTCAGGTGAT | 151112 |
rs11903271 | snp | A/G | 0.234982 | 0.249549 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186837637 | atatatattatatat[A/G]tatttatataaataA | 151112 |
rs12612668 | snp | A/C | 0.315516 | 0.241263 | utr-variant-3-prime | ZSWIM2 | GRCh38.p7 | 2:186827717 | TTAAGTAAAACATTT[A/C]TAAAATCAGAGTAAA | 151112 |
rs12616053 | snp | C/T | 0.316485 | 0.240998 | utr-variant-3-prime | ZSWIM2 | GRCh38.p7 | 2:186827578 | ATAGGTTTGTGGTAA[C/T]TACTAGTGCAAGAAA | 151112 |
rs12693456 | snp | C/G | 0.261884 | 0.249717 | upstream-variant-2KB | ZSWIM2 | GRCh38.p7 | 2:186849802 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 151112 |
rs12999133 | snp | C/T | 0 | 0 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186836760 | GGGGGTTACTCACAG[C/T]GAAAATTGTTTGCTC | 151112 |
rs13390084 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | ZSWIM2 | GRCh38.p7 | 2:186848977 | TTACTCGGAAATCCA[C/T]GTATTCCGGCTCCTC | 151112 |
rs13399866 | snp | A/G | 0.287085 | 0.247234 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186835931 | GTAGGGTCACTAGTG[A/G]GCAGGGGGCAGGATA | 151112 |
rs13400804 | snp | A/G | 0.262159 | 0.249704 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186836795 | AATTACTATGTTTTT[A/G]TAGTTGTTGAAGTAT | 151112 |
rs13401173 | snp | C/T | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186831319 | TATATCAACTGAAGT[C/T]TGGATACAAACTtac | 151112 |
rs13401579 | snp | A/G | 0.288127 | 0.247076 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186831517 | tgacccagccatccc[A/G]ttactgggtatatac | 151112 |
rs13404398 | snp | A/C | 0.287867 | 0.247116 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186832009 | tgcacatgtacccta[A/C]aacttaaagtataat | 151112 |
rs13404635 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186832238 | tcctgcctcagcctc[A/C]cgagtagctgggatt | 151112 |
rs13406781 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186845186 | AAAAAAATTTTTTTT[A/T]AATTTTACCAATAAA | 151112 |
rs13407429 | snp | A/G | 0.249038 | 0.249998 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186845771 | GTCAATTACCCTACA[A/G]ATAGATTCTCACACT | 151112 |
rs13407627 | snp | A/T | 0.132066 | 0.220435 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186829465 | GATAACTAAAGTAGA[A/T]AAAGGAATCTAACTT | 151112 |
rs13414169 | snp | G/T | 0.262159 | 0.249704 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186836822 | GTATAAGATATGAAA[G/T]AAAACAAAACCTGTA | 151112 |
rs13414172 | snp | A/T | 0.132066 | 0.220435 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186836834 | AAATAAAACAAAACC[A/T]GTACTCATTGCCATT | 151112 |
rs13417791 | snp | A/T | 0.490175 | 0.0693959 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186831910 | ggatagcattaggag[A/T]tatacctaatgctaa | 151112 |
rs13426438 | snp | A/G | 0.287606 | 0.247155 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186831234 | TTGCAAAGCCTTTGT[A/G]TAGGCTCATTTTACG | 151112 |
rs13426924 | snp | A/G | 0.493793 | 0.055364 | intron-variant | ZSWIM2 | GRCh38.p7 | 2:186831663 | GGATTAAGAAAATGT[A/G]GCACATATACACCAT | 151112 |