SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs140764 | in-del | -/ATT/TAT | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75135460 | GGAAAATTATCTTGT[-/ATT/TAT]ATTTCTTTTAGAATT | 26578 |
rs764437 | snp | A/G | 0.385168 | 0.210309 | intron-variant | OSTF1 | GRCh38.p7 | 9:75135330 | CCCATTCTTTTATGT[A/G]TGATCTGCTTTTTCT | 26578 |
rs1009282 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | OSTF1 | GRCh38.p7 | 9:75138051 | TTTACATCTAGCACC[C/T]GCTCAGCTCAAAGCA | 26578 |
rs1009376 | snp | C/T | 0.19459 | 0.243782 | intron-variant | OSTF1 | GRCh38.p7 | 9:75091615 | AAAGACAGCATGGGA[C/T]TGGGGGCTTTGGGGT | 26578 |
rs1010198 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | OSTF1 | GRCh38.p7 | 9:75093812 | AGGTATAAAAAGTAT[C/T]AAGTTTATAAAAGAA | 26578 |
rs1033777 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | OSTF1 | GRCh38.p7 | 9:75107351 | ATTTTTTAGTACCCA[C/T]GGGGTATAAATTAAG | 26578 |
rs1052199 | snp | A/G | 0.472803 | 0.113397 | utr-variant-3-prime | OSTF1 | GRCh38.p7 | 9:75146941 | ATTCTTGGCACATTT[A/G]TGTTCACCAAAGTAG | 26578 |
rs1407376 | snp | A/G | 0.25214 | 0.249991 | downstream-variant-500B | OSTF1 | GRCh38.p7 | 9:75147533 | AAAATTTATTTCCTT[A/G]TGATAGATGCCATAC | 26578 |
rs1570284 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | OSTF1 | GRCh38.p7 | 9:75091327 | gtgatccaccctcct[C/T]cgcttcccaaagtgt | 26578 |
rs1804671 | snp | C/T | | | missense | OSTF1 | GRCh38.p7 | 9:75146733 | CTCGATGATGAAGAC[C/T]CAGATTAATTCCTTT | 26578 |
rs1977240 | snp | C/T | 0.396546 | 0.202545 | intron-variant | OSTF1 | GRCh38.p7 | 9:75095873 | CAATTAAACAAGTTA[C/T]TGGTGTGACTGCTGT | 26578 |
rs1977241 | snp | C/T | 0.405603 | 0.195673 | intron-variant | OSTF1 | GRCh38.p7 | 9:75095897 | CTGCTGTGGCCCCCC[C/T]TTTTTTTTTTTTGAG | 26578 |
rs1977242 | snp | A/T | 0.188 | 0.24219 | intron-variant | OSTF1 | GRCh38.p7 | 9:75096067 | tggctaatttttggt[A/T]tttttagtagagtca | 26578 |
rs2025159 | snp | A/G | 0.384401 | 0.210799 | intron-variant | OSTF1 | GRCh38.p7 | 9:75137759 | CCTGTGTATCATGGA[A/G]TAGTTATGATAAAAT | 26578 |
rs2025160 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | OSTF1 | GRCh38.p7 | 9:75137924 | GAATGTATGTGTACA[C/T]GTGTGTTGGGGAGAT | 26578 |
rs2146044 | snp | C/T | 0.191039 | 0.242948 | synonymous-codon | OSTF1 | GRCh38.p7 | 9:75146726 | GGACTATCTCGATGA[C/T]GAAGACTCAGATTAA | 26578 |
rs2146048 | snp | G/T | 0.321292 | 0.23962 | intron-variant | OSTF1 | GRCh38.p7 | 9:75099403 | ACTACAGGCATGTGC[G/T]GCCAAGCCCAACTAT | 26578 |
rs2146049 | snp | A/G | 0.238171 | 0.24972 | intron-variant | OSTF1 | GRCh38.p7 | 9:75115471 | AAATTTTTATCTTTA[A/G]TAGAGATGGGGTTTC | 26578 |
rs2181116 | snp | A/G | 0.35574 | 0.226537 | intron-variant | OSTF1 | GRCh38.p7 | 9:75095641 | ATTTGGTATGTGCAC[A/G]GAGAACTGTGAACCA | 26578 |
rs2208688 | snp | G/T | 0.307919 | 0.243198 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NMRK1, OSTF1 | GRCh38.p7 | 9:75086912 | CTCAAGGCTGGGTTT[G/T]TTTTTTTTTTTTAAG | 26578 |
rs2273769 | snp | C/T | 0.279336 | 0.248273 | synonymous-codon | OSTF1 | GRCh38.p7 | 9:75137594 | GGGTTATGCAGATAT[C/T]GTCCAGTTGCTTCTG | 26578 |
rs2273770 | snp | C/T | 0.44546 | 0.155869 | intron-variant | OSTF1 | GRCh38.p7 | 9:75140553 | ATTGAAGTCAAGCCC[C/T]ACAGGGACCATAAAC | 26578 |
rs2281661 | snp | A/T | 0.390677 | 0.212666 | intron-variant | OSTF1 | GRCh38.p7 | 9:75131495 | GCATTTAACTCAGGT[A/T]TGCGGGTTTGTTTGT | 26578 |
rs2281662 | snp | C/T | 0.412917 | 0.189626 | intron-variant | OSTF1 | GRCh38.p7 | 9:75131888 | GATTTCAATTAGCTT[C/T]GACAAGTGCATACAC | 26578 |
rs2295861 | snp | C/T | 0.393803 | 0.204501 | intron-variant | OSTF1 | GRCh38.p7 | 9:75130508 | GTACTCCCTAGGAGC[C/T]AGATAATTTGAAAAG | 26578 |
rs2295862 | snp | A/G | 0.000642859 | 0.0179169 | missense | OSTF1 | GRCh38.p7 | 9:75130588 | ACCAGAGCGATACCA[A/G]TTGGTGGAAAGGCAC | 26578 |
rs2376398 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | OSTF1 | GRCh38.p7 | 9:75092028 | TAGCCATGTTTCTTA[C/T]AGCTTCTTTCAGAGC | 26578 |
rs2376399 | snp | C/T | 0.39979 | 0.200158 | intron-variant | OSTF1 | GRCh38.p7 | 9:75136767 | ggttgggcttctcca[C/T]agggtgatgtggtga | 26578 |
rs3060046 | in-del | -/TTTC | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75093061 | ctCtctctttctttc[-/TTTC]tttttttttttttgg | 26578 |
rs3758189 | snp | G/T | 0.380724 | 0.213099 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NMRK1, OSTF1 | GRCh38.p7 | 9:75086992 | CTTACTGCAACCTCC[G/T]CCTTCTGGGTTCAAG | 26578 |
rs3758190 | snp | A/T | 0.193653 | 0.243567 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NMRK1, OSTF1 | GRCh38.p7 | 9:75087267 | CTTAGGTAAACAGTT[A/T]TTTCTTTCCCCAAAT | 26578 |
rs3780177 | snp | C/T | 0.480144 | 0.097642 | intron-variant | OSTF1 | GRCh38.p7 | 9:75093064 | TCTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGG | 26578 |
rs3780178 | snp | C/T | 0.376394 | 0.215696 | intron-variant | OSTF1 | GRCh38.p7 | 9:75093236 | AATGAGTACAACCTC[C/T]TAGTTTTACACATAT | 26578 |
rs3780179 | snp | C/T | 0.348354 | 0.22984 | intron-variant | OSTF1 | GRCh38.p7 | 9:75100586 | AATACAAAAATTAGC[C/T]GGGCCGTGGTGGCGC | 26578 |
rs3780180 | snp | C/T | 0.366885 | 0.220993 | intron-variant | OSTF1 | GRCh38.p7 | 9:75112968 | AAATACTGTATTTCT[C/T]CTGGCAGCTCCTCCT | 26578 |
rs3812513 | snp | C/G | 0.221439 | 0.248363 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NMRK1, OSTF1 | GRCh38.p7 | 9:75087850 | TGATAGGTGGCCTGC[C/G]GAGGAGGACGTGTAC | 26578 |
rs3824348 | snp | A/T | 0.464523 | 0.128375 | intron-variant | OSTF1 | GRCh38.p7 | 9:75123635 | ATCTGTTGTTAAAAT[A/T]ATGAAATTACCGTGT | 26578 |
rs3837221 | in-del | -/GTGTGTGTGTGTGT | | | upstream-variant-2KB, intron-variant | NMRK1, OSTF1 | GRCh38.p7 | 9:75090295 | GAGGGACATTGACAG[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 26578 |
rs4013823 | in-del | -/GGGGAAGAT | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75132323 | AACAGGGATGAACCT[-/GGGGAAGAT]CCTTGACCAAACAAC | 26578 |
rs4013824 | in-del | -/TTGA | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75132334 | ACCTGGGGAAGATCC[-/TTGA]CCAAACAACGATCAG | 26578 |
rs4376557 | snp | A/G | 0.350982 | 0.228698 | intron-variant | OSTF1 | GRCh38.p7 | 9:75145627 | aatgtagcaagggca[A/G]gataaatgcttgatt | 26578 |
rs4376558 | snp | C/G | 0.370365 | 0.219117 | intron-variant | OSTF1 | GRCh38.p7 | 9:75145834 | CTCAGACCCTTTCAC[C/G]TGATGCTGTCTTTGT | 26578 |
rs4445291 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | OSTF1 | GRCh38.p7 | 9:75136689 | gagccaccatgcctg[A/G]ccCTTATCCATTCAT | 26578 |
rs4532667 | snp | C/T | 0.428635 | 0.174898 | intron-variant | OSTF1 | GRCh38.p7 | 9:75142034 | ATTACAGGCGAGAGC[C/T]GCTGTGCCCAGCCTC | 26578 |
rs4744736 | snp | C/G | 0.39214 | 0.205661 | intron-variant | OSTF1 | GRCh38.p7 | 9:75105984 | GTTAATAAACAGAAC[C/G]CTCTTGTCAGAAAAC | 26578 |
rs4745378 | snp | A/G | 0.323197 | 0.239044 | intron-variant | OSTF1 | GRCh38.p7 | 9:75095504 | CCAATGCTGAGTAAG[A/G]GTTTGCTGGGCAGCA | 26578 |
rs4745379 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | OSTF1 | GRCh38.p7 | 9:75111136 | TAAGCCCCAGGCCCG[C/T]CTAAGTGCTGTTTCA | 26578 |
rs4745380 | snp | C/T | 0.393803 | 0.204501 | intron-variant | OSTF1 | GRCh38.p7 | 9:75131083 | GAGAGACACGGCTCC[C/T]GCCATGAAGCTGCTT | 26578 |
rs4745381 | snp | A/G | 0.431029 | 0.17242 | intron-variant | OSTF1 | GRCh38.p7 | 9:75134733 | GCTGCCCCAGCTCTC[A/G]TCTTTCAGCACCCCA | 26578 |
rs5898395 | in-del | -/TAT | 0.386123 | 0.209692 | intron-variant | OSTF1 | GRCh38.p7 | 9:75135459 | TGGAAAATTATCTTG[-/TAT]TATTTCTTTTAGAAT | 26578 |
rs5898396 | in-del | -/T | 0.381697 | 0.212499 | utr-variant-3-prime | OSTF1 | GRCh38.p7 | 9:75147004 | AAAGGAATTTTAAGA[-/T]TTTTTTTTTTCTTTA | 26578 |
rs6560421 | snp | A/G | 0.456214 | 0.141336 | intron-variant | OSTF1 | GRCh38.p7 | 9:75129500 | TACTAACATTACAAA[A/G]AGAAGCCGACTAGAT | 26578 |
rs6560423 | snp | A/G | 0.472989 | 0.113031 | intron-variant | OSTF1 | GRCh38.p7 | 9:75143203 | GCCTTGGCCTCCCAA[A/G]GTAGTTGTTGTCTAC | 26578 |
rs6560424 | snp | A/G | 0.472803 | 0.113397 | intron-variant | OSTF1 | GRCh38.p7 | 9:75143249 | GTGGATTTTTTAATA[A/G]GTACAAAAATTCACA | 26578 |
rs7020233 | snp | A/G | | | upstream-variant-2KB, intron-variant | NMRK1, OSTF1 | GRCh38.p7 | 9:75089880 | GTTCCTGCAGTTGGA[A/G]TATGAAGTCCCTTTA | 26578 |
rs7022928 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | OSTF1 | GRCh38.p7 | 9:75136486 | caacctctgcctccc[A/G]ggttcaagctattct | 26578 |
rs7023958 | snp | G/T | 0.397271 | 0.202018 | intron-variant | OSTF1 | GRCh38.p7 | 9:75096374 | GCATCCCTTATAATT[G/T]GATAAGCTATTTTGG | 26578 |
rs7024550 | snp | A/T | 0 | 0 | intron-variant | OSTF1 | GRCh38.p7 | 9:75145106 | ttCATtctatcaatc[A/T]atcaatcatgaatca | 26578 |
rs7026023 | snp | A/C | 0.494609 | 0.0516363 | intron-variant | OSTF1 | GRCh38.p7 | 9:75133011 | CACACACACACACAC[A/C]CCCCTATATATTTTT | 26578 |
rs7027731 | snp | C/T | 0 | 0 | intron-variant | OSTF1 | GRCh38.p7 | 9:75145015 | actgcattcccatgg[C/T]gttatttgtcatgtt | 26578 |
rs7029215 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | OSTF1 | GRCh38.p7 | 9:75140124 | GAAATCACAGACCAA[A/T]ACGTGTAGTACGATT | 26578 |
rs7034779 | snp | A/G | 0.395087 | 0.203592 | intron-variant | OSTF1 | GRCh38.p7 | 9:75107281 | ATTCAAATATGCCTC[A/G]TAGAAATAATTAATA | 26578 |
rs7038295 | snp | A/C | 0.197393 | 0.244402 | intron-variant | OSTF1 | GRCh38.p7 | 9:75092414 | AGACACTGGGGTTCC[A/C]AGGAACAATAATCTA | 26578 |
rs7039612 | snp | C/T | 0.451483 | 0.148002 | intron-variant | OSTF1 | GRCh38.p7 | 9:75145162 | ctatctatctatcta[C/T]ctatctatctatcta | 26578 |
rs7039751 | snp | A/G | 0.384209 | 0.210922 | intron-variant | OSTF1 | GRCh38.p7 | 9:75136540 | tgggactacaggccc[A/G]tgccactggcctggc | 26578 |
rs7040169 | snp | A/G | 0.456214 | 0.141336 | intron-variant | OSTF1 | GRCh38.p7 | 9:75133061 | TAAGTATACCCATTT[A/G]GGCAACTATTCCCAT | 26578 |
rs7040349 | snp | A/G | 0.327445 | 0.237702 | intron-variant | OSTF1 | GRCh38.p7 | 9:75133235 | GACATTGATTTAAAA[A/G]CAAAATAAAAAGTGA | 26578 |
rs7040987 | snp | C/T | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75132994 | acacacacacacaca[C/T]acacacacacacaca | 26578 |
rs7042557 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | OSTF1 | GRCh38.p7 | 9:75093302 | TTGCAGTTCAATTAG[C/T]GTGAATCTGTCTGGC | 26578 |
rs7043098 | snp | C/T | 0.399432 | 0.200425 | intron-variant | OSTF1 | GRCh38.p7 | 9:75136547 | acaggcccatgccac[C/T]ggcctggcttatttt | 26578 |
rs7469648 | snp | A/C | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75124516 | tcacaaataagtgag[A/C]acatgcgatgtttgt | 26578 |
rs7847469 | snp | A/G | 0.190833 | 0.242898 | intron-variant | OSTF1 | GRCh38.p7 | 9:75129969 | gtctttcagagatac[A/G]tactgaaatatttac | 26578 |
rs7847507 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | OSTF1 | GRCh38.p7 | 9:75130042 | caggaggggagggac[A/G]tcatgggggcatata | 26578 |
rs7847600 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | OSTF1 | GRCh38.p7 | 9:75130071 | tatgaaacaatattg[A/G]tcattaataaatgat | 26578 |
rs7847851 | snp | C/T | 0.140919 | 0.224948 | intron-variant | OSTF1 | GRCh38.p7 | 9:75109827 | ggctgtactaattta[C/T]gctcccactagcagt | 26578 |
rs7848243 | snp | C/T | 0.141258 | 0.225111 | intron-variant | OSTF1 | GRCh38.p7 | 9:75110114 | agaatccatagttta[C/T]gttagggtttgctct | 26578 |
rs7849309 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | OSTF1 | GRCh38.p7 | 9:75138827 | AAAGTATAATATAGT[A/G]TATGATTAGTCACAG | 26578 |
rs7852759 | snp | C/T | 0.433527 | 0.169758 | intron-variant | OSTF1 | GRCh38.p7 | 9:75139058 | tttctttctttcttt[C/T]ttttttGAAACTGGG | 26578 |
rs7853141 | snp | A/G | 0.121022 | 0.21416 | intron-variant | OSTF1 | GRCh38.p7 | 9:75139574 | gctgggattacaggc[A/G]tgcgccaccacactt | 26578 |
rs7855951 | snp | G/T | 0.309154 | 0.242901 | intron-variant | OSTF1 | GRCh38.p7 | 9:75124853 | GGAGATTTGACTTTT[G/T]TGATTTTAGAAGGAG | 26578 |
rs7857206 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | OSTF1 | GRCh38.p7 | 9:75125208 | CAACCTTAATGTGGG[C/T]GGGAGGTTGGGGCAG | 26578 |
rs7857698 | snp | A/G | 0.130694 | 0.219696 | intron-variant | OSTF1 | GRCh38.p7 | 9:75133673 | TGGAAAACAGCAGTA[A/G]TATAAAAACAAAACC | 26578 |
rs7859225 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | OSTF1 | GRCh38.p7 | 9:75128949 | accaacccaataata[A/G]tatgttattttccat | 26578 |
rs7859460 | snp | A/G | 0.190519 | 0.242821 | intron-variant | OSTF1 | GRCh38.p7 | 9:75129131 | agactcccactggcc[A/G]aagataggacaattt | 26578 |
rs7861081 | snp | C/T | 0.487746 | 0.0773096 | intron-variant | OSTF1 | GRCh38.p7 | 9:75133854 | ATACTTTTTCTGTTG[C/T]AATCAATAATAATGA | 26578 |
rs7862075 | snp | C/T | 0.472989 | 0.113031 | intron-variant | OSTF1 | GRCh38.p7 | 9:75143720 | GCCAGGGTGATGGGA[C/T]TGAGGTAAAATGAAC | 26578 |
rs7862639 | snp | C/G | 0.226779 | 0.248919 | intron-variant | OSTF1 | GRCh38.p7 | 9:75138867 | CCCTCAGGAGTTTTT[C/G]ATCTGTAGCACACTG | 26578 |
rs7863446 | snp | A/G | 0.464309 | 0.12873 | intron-variant | OSTF1 | GRCh38.p7 | 9:75130045 | GAGGGGAGGGACGTC[A/G]TGGGGGCATATATGA | 26578 |
rs7865466 | snp | A/C | | | intron-variant | OSTF1 | GRCh38.p7 | 9:75141310 | tctcaaaaaaagaaa[A/C]ccaaaaaaaaaaaaa | 26578 |
rs7868101 | snp | C/T | 0.394171 | 0.204242 | intron-variant | OSTF1 | GRCh38.p7 | 9:75120536 | GACTGGAGGTGACTC[C/T]TGACTCTATCTCCTC | 26578 |
rs7868417 | snp | A/G | 0.393619 | 0.204631 | intron-variant | OSTF1 | GRCh38.p7 | 9:75124476 | gctctctgtccatga[A/G]ttcaattgttttgat | 26578 |
rs7869308 | snp | C/T | 0.483708 | 0.088773 | intron-variant | OSTF1 | GRCh38.p7 | 9:75135884 | TAGAGGCCACCCCTC[C/T]CTGTAGACAGCTCAC | 26578 |
rs7871013 | snp | C/G | 0.469642 | 0.119404 | intron-variant | OSTF1 | GRCh38.p7 | 9:75146220 | CTTTTGCTTTATTGT[C/G]GGTGTTTTCTACATT | 26578 |
rs7872448 | snp | C/T | 0.425432 | 0.178112 | intron-variant | OSTF1 | GRCh38.p7 | 9:75134052 | AAGCCTATCTTATTT[C/T]AGCTAATAAACATGT | 26578 |
rs7873449 | snp | A/C | 0.190519 | 0.242821 | intron-variant | OSTF1 | GRCh38.p7 | 9:75128855 | CCTTCATCTGAATTG[A/C]AAGGATCACATTGTA | 26578 |
rs9695215 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | OSTF1 | GRCh38.p7 | 9:75127302 | CTCTATTTTGATATA[C/T]AAATGTCTTGCTTTG | 26578 |
rs9695333 | snp | A/G | 0.141596 | 0.225274 | intron-variant | OSTF1 | GRCh38.p7 | 9:75120686 | CCATCTGTCGTCTGA[A/G]CTAGATTGGCATTCC | 26578 |
rs9695750 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | OSTF1 | GRCh38.p7 | 9:75120171 | cccccaTAAGCCCAT[C/T]GTAAAGTTGACAAAT | 26578 |
rs9776041 | snp | A/G | 0.191147 | 0.242974 | intron-variant | OSTF1 | GRCh38.p7 | 9:75127928 | GAGAAAATGTAGATA[A/G]TATATCCTCAGTTTT | 26578 |
rs9776186 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | OSTF1 | GRCh38.p7 | 9:75128271 | ATTGTACCCTGGTAA[C/T]TGGCCTAACCACACA | 26578 |