SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1565748 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASB7 | GRCh38.p7 | 15:100638289 | TACATTATTGCTTGC[C/T]GTTTACTATCATATT | 140460 |
rs1565750 | snp | G/T | 0.0718919 | 0.175435 | intron-variant | ASB7 | GRCh38.p7 | 15:100636482 | TGACACAGGCACAGT[G/T]GGGGGATCTTTGGGA | 140460 |
rs1873956 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ASB7 | GRCh38.p7 | 15:100607843 | CAAACTATTTCTCCC[A/C]ACAAGAAAGATTCAC | 140460 |
rs1873958 | snp | C/T | 0.487305 | 0.0786545 | intron-variant | ASB7 | GRCh38.p7 | 15:100607521 | AAAAACATACACACA[C/T]GTCATGCACACATGA | 140460 |
rs1873959 | snp | A/G | 0.0517044 | 0.152246 | upstream-variant-2KB, intron-variant | LINS1, ASB7 | GRCh38.p7 | 15:100603175 | GGTGTAGTGTCTCAG[A/G]GGTGGGGAGGGGGGA | 140460 |
rs1979710 | snp | C/G | 0.37138 | 0.218556 | intron-variant | ASB7 | GRCh38.p7 | 15:100619907 | AGAGCCACACTGTTA[C/G]CCTTTTGGAATACAG | 140460 |
rs1979711 | snp | C/T | 0.369754 | 0.219451 | intron-variant | ASB7 | GRCh38.p7 | 15:100619876 | GTAGTATCATTTACT[C/T]GACTCAGACTCGCTC | 140460 |
rs2029699 | snp | C/T | 0.453453 | 0.145282 | intron-variant | ASB7 | GRCh38.p7 | 15:100610309 | gacggggtttcaccg[C/T]gttagccaggatggt | 140460 |
rs2029700 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ASB7 | GRCh38.p7 | 15:100610223 | acaggcgtgagccac[C/T]gcgcccggccACAAG | 140460 |
rs2047091 | snp | C/T | 0.0444908 | 0.142359 | upstream-variant-2KB, intron-variant | LINS1, ASB7 | GRCh38.p7 | 15:100604040 | ATTTTTAAAAGTTCT[C/T]CTAGAAAATCTGAGG | 140460 |
rs2172576 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | ASB7 | GRCh38.p7 | 15:100647235 | AAAGGAGTTTTGAAA[A/C]CAAAAAGTTTGAGAA | 140460 |
rs2172577 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASB7 | GRCh38.p7 | 15:100636214 | caaacctccaccaca[C/G]aatttggagaggaaa | 140460 |
rs2279594 | snp | C/T | 0.456095 | 0.141508 | utr-variant-3-prime | ASB7 | GRCh38.p7 | 15:100649691 | TTTGCCGTGTAAACA[C/T]GGATATGATAAAGTG | 140460 |
rs2411839 | snp | A/G | 0.414905 | 0.187899 | intron-variant | ASB7 | GRCh38.p7 | 15:100632053 | GTGGGCGGCTGCCGT[A/G]TGTCCCTGAGCCCTC | 140460 |
rs2411841 | snp | C/T | 0.438666 | 0.164028 | downstream-variant-500B | ASB7 | GRCh38.p7 | 15:100652046 | GTTTAGACCACAGCG[C/T]TTCTAAACGTAGGAC | 140460 |
rs3084805 | in-del | -/TG | | | intron-variant | ASB7 | GRCh38.p7 | 15:100644837 | ACATGAGTGTGTGTG[-/TG]TCACATCCCTGTACA | 140460 |
rs3764202 | snp | C/T | 0.154661 | 0.231107 | upstream-variant-2KB, intron-variant | LINS1, ASB7 | GRCh38.p7 | 15:100603166 | TTCCTGAGCTCCCCC[C/T]TCCCCACCTCTGAGA | 140460 |
rs3794503 | snp | A/C | 0.257176 | 0.249897 | intron-variant, upstream-variant-2KB | LINS1, ASB7 | GRCh38.p7 | 15:100601691 | TGTTCACTGTTGTCT[A/C]CCCAGGGACTAGAAC | 140460 |
rs3794504 | snp | C/T | 0.446118 | 0.155041 | intron-variant, upstream-variant-2KB | LINS1, ASB7 | GRCh38.p7 | 15:100601933 | CGGGGTCTCAAGGAC[C/T]GACAGCCGCGCCAAG | 140460 |
rs3794505 | snp | A/G | 0.227664 | 0.249 | intron-variant, upstream-variant-2KB | LINS1, ASB7 | GRCh38.p7 | 15:100601941 | CAAGGACCGACAGCC[A/G]CGCCAAGACCGGGCA | 140460 |
rs3803440 | snp | C/T | 0.420733 | 0.18262 | intron-variant | ASB7 | GRCh38.p7 | 15:100632520 | CTTTTCATGAGAAAG[C/T]TCAGTCCAGAGCATC | 140460 |
rs3933897 | snp | G/T | 0.476833 | 0.105105 | intron-variant | ASB7 | GRCh38.p7 | 15:100610423 | actgcaacctccacc[G/T]cccgggttcacacct | 140460 |
rs3935404 | snp | A/G | 0.398354 | 0.201224 | intron-variant | ASB7 | GRCh38.p7 | 15:100643735 | GAGGCTGAGGCAGGC[A/G]GATCACGAGGTCAGG | 140460 |
rs4073788 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ASB7 | GRCh38.p7 | 15:100643701 | ttgagaccatcctgg[C/T]caacatggtgaaacc | 140460 |
rs4131339 | snp | A/C/G | 0.054884 | 0.157042 | intron-variant | ASB7 | GRCh38.p7 | 15:100647019 | ATGTGAAAGAATGAC[A/C/G]TTCTTGTTAAATTTT | 140460 |
rs4398095 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ASB7 | GRCh38.p7 | 15:100631849 | TAATTGTTTTTCAAG[A/G]TGAAGTGTGTAACTA | 140460 |
rs4465593 | snp | C/T | 0.124144 | 0.21601 | intron-variant | ASB7 | GRCh38.p7 | 15:100636784 | tttatGTTAGAATGA[C/T]GTTTTTCagtgtgga | 140460 |
rs4553607 | snp | A/G | 0.241627 | 0.24986 | intron-variant | ASB7 | GRCh38.p7 | 15:100643084 | ctggctcaggtggcc[A/G]gcaagttggtgctgg | 140460 |
rs4965323 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ASB7 | GRCh38.p7 | 15:100611679 | GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 140460 |
rs4965324 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | ASB7 | GRCh38.p7 | 15:100611899 | atcatggctcactgc[A/C]gctttgatctcctgg | 140460 |
rs4965325 | snp | A/G | 0.365439 | 0.221752 | intron-variant | ASB7 | GRCh38.p7 | 15:100629194 | CCGTGTTTTTTGTGT[A/G]TATCTTTTTAAACAC | 140460 |
rs4965326 | snp | A/G | 0.416708 | 0.186302 | downstream-variant-500B, intron-variant | ASB7 | GRCh38.p7 | 15:100630413 | TGAGGAGTTAGAGGG[A/G]GAATTTTGGATCTTA | 140460 |
rs4965682 | snp | C/T | 0.465788 | 0.126237 | intron-variant | ASB7 | GRCh38.p7 | 15:100612022 | gggactataggcttg[C/T]accaccacacccagc | 140460 |
rs4965683 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | ASB7 | GRCh38.p7 | 15:100612540 | GTTAATACTCAACAT[A/C]TTATTCTCTCTCCTT | 140460 |
rs4965684 | snp | A/G | 0.35445 | 0.227135 | intron-variant | ASB7 | GRCh38.p7 | 15:100614207 | TGAACCCAGTGGGTG[A/G]AGGTTGCAGTGAGCT | 140460 |
rs4965685 | snp | A/G | 0.494484 | 0.0522255 | intron-variant | ASB7 | GRCh38.p7 | 15:100618711 | GCCAGCTGATCCTTT[A/G]TAAACTATGTATTCA | 140460 |
rs4965686 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | ASB7 | GRCh38.p7 | 15:100619073 | AAGAGTGAATTTAAG[G/T]GCCATGTGTAATAAG | 140460 |
rs4965687 | snp | C/T | 0.497211 | 0.037236 | intron-variant | ASB7 | GRCh38.p7 | 15:100620046 | AATGGTTGCATGTGA[C/T]GAGTGGCTGCCATAT | 140460 |
rs4965688 | snp | A/G | 0.382473 | 0.212016 | intron-variant | ASB7 | GRCh38.p7 | 15:100623851 | actactgagtatcca[A/G]aagaaaagaaatcag | 140460 |
rs4965689 | snp | A/C | 0.383053 | 0.211653 | intron-variant | ASB7 | GRCh38.p7 | 15:100629009 | TGTAATTTAGAGCAG[A/C]AGATGTTGCTACACA | 140460 |
rs4965691 | snp | A/T | 0.499424 | 0.0169631 | intron-variant | ASB7 | GRCh38.p7 | 15:100641021 | GTAATTCTTTAAATT[A/T]TGCTCTTTTGTGAGA | 140460 |
rs4965692 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | ASB7 | GRCh38.p7 | 15:100648135 | ATATCCACCATCCCA[C/G]GGTTGTGAAAAGGAT | 140460 |
rs5814978 | in-del | -/AA/AAA | 0.5 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100610494 | CTCAAAAAAAAAAAA[-/AA/AAA]GAGGCAATCTTGTTT | 140460 |
rs5814979 | in-del | -/GT | 0.495855 | 0.045338 | intron-variant | ASB7 | GRCh38.p7 | 15:100644828 | CCAAGAGGCACATGA[-/GT]GTGTGTGTGTCACAT | 140460 |
rs5814980 | in-del | -/CTT | 0 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100647024 | AAGAATGACGTTCTT[-/CTT]GTTAAATTTTTTTTT | 140460 |
rs6598366 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | ASB7 | GRCh38.p7 | 15:100608186 | GTGTGAGGCTCATCA[C/T]TGGGGACACTGATTT | 140460 |
rs6598367 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | ASB7 | GRCh38.p7 | 15:100608349 | CTTGAGGAGAGACTA[C/T]CTATACAAATTATTT | 140460 |
rs6598368 | snp | C/T | 0.497416 | 0.0358495 | intron-variant | ASB7 | GRCh38.p7 | 15:100615521 | TTTATTTTTTGAGAA[C/T]GGCTGGAATTTTCAC | 140460 |
rs6598369 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ASB7 | GRCh38.p7 | 15:100615807 | CATAACAGTTAATTT[A/C]GTGATAGTTCCTTAT | 140460 |
rs6598370 | snp | G/T | 0.254944 | 0.249951 | intron-variant | ASB7 | GRCh38.p7 | 15:100646629 | TTTCTTGTGATCAGT[G/T]TAGAAGCTTGTTTGC | 140460 |
rs7162990 | snp | C/G | 0.142609 | 0.225759 | intron-variant | ASB7 | GRCh38.p7 | 15:100611012 | ATTTCACTTTGGACT[C/G]TTACTGTTTCCATGA | 140460 |
rs7164170 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ASB7 | GRCh38.p7 | 15:100605625 | TATATGGGCATATCT[A/G]TTACCTGACTTTCAG | 140460 |
rs7165248 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASB7 | GRCh38.p7 | 15:100605157 | AGTTTTTCTAAGATT[A/G]GGGAATATGTGTAAA | 140460 |
rs7165626 | snp | C/T | 0.432357 | 0.171014 | intron-variant | ASB7 | GRCh38.p7 | 15:100633347 | TTTGGGAGGCTGAGG[C/T]GGGTGGGTCACCTGA | 140460 |
rs7166822 | snp | G/T | 0.451856 | 0.147493 | upstream-variant-2KB, utr-variant-5-prime | LINS1, ASB7 | GRCh38.p7 | 15:100602244 | GCATGCGCAGAGACC[G/T]CCTTCGGCGAATAGT | 140460 |
rs7167073 | snp | A/T | 0.3744 | 0.216852 | intron-variant | ASB7 | GRCh38.p7 | 15:100620286 | TACTGTATTGTTTTT[A/T]AAAAATGTATTGTTG | 140460 |
rs7167468 | snp | C/T | 0.24932 | 0.249999 | intron-variant, upstream-variant-2KB | LINS1, ASB7 | GRCh38.p7 | 15:100601260 | aagaaaagtaattta[C/T]tgtctagttttggag | 140460 |
rs7168464 | snp | A/G | 0.420415 | 0.182917 | intron-variant | ASB7 | GRCh38.p7 | 15:100630716 | TCTGGCCCACTTTGT[A/G]TAGTAACGCGTGCGT | 140460 |
rs7168512 | snp | G/T | 0.495745 | 0.0459295 | intron-variant | ASB7 | GRCh38.p7 | 15:100646428 | CACAACTTCTTTTAA[G/T]GAGGTGTTCTCCCGT | 140460 |
rs7169399 | snp | C/G | 0.402454 | 0.198136 | intron-variant | ASB7 | GRCh38.p7 | 15:100648091 | TACATCTGATACTCA[C/G]TTTTCTTATTGGTAA | 140460 |
rs7178447 | snp | A/C | 0.102014 | 0.201495 | intron-variant | ASB7 | GRCh38.p7 | 15:100619718 | CCACCGATCAGTGAT[A/C]ACACAGAGCTAGCCA | 140460 |
rs7180007 | snp | C/G | 0 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100617049 | accttttccttacct[C/G]taatatgactgattg | 140460 |
rs7180565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASB7 | GRCh38.p7 | 15:100631214 | tgatgttggaaatgg[C/T]ctctccttgctgtcc | 140460 |
rs8028602 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ASB7 | GRCh38.p7 | 15:100621870 | gaatggtgaaaaaaa[A/G]aaaacaggagaaaag | 140460 |
rs8032720 | snp | A/C | 0.482609 | 0.0916147 | intron-variant | ASB7 | GRCh38.p7 | 15:100606419 | TGCAAAAAGTCATTA[A/C]TGTCTAATCATTTAT | 140460 |
rs8033048 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | ASB7 | GRCh38.p7 | 15:100606611 | CTTCACTTGGCATCT[A/G]TATGGAAATTAGATG | 140460 |
rs8036451 | snp | C/T | 0.370772 | 0.218893 | intron-variant | ASB7 | GRCh38.p7 | 15:100631845 | TTTGTAATTGTTTTT[C/T]AAGGTGAAGTGTGTA | 140460 |
rs8036653 | snp | A/G | 0.441841 | 0.160303 | intron-variant | ASB7 | GRCh38.p7 | 15:100635128 | GTACAGCACTGTTGG[A/G]GGGTCACCTTGTCAC | 140460 |
rs8036769 | snp | C/T | 0.371785 | 0.218331 | intron-variant | ASB7 | GRCh38.p7 | 15:100632043 | GGACAAGCACGTGGG[C/T]GGCTGCCGTGTGTCC | 140460 |
rs8042302 | snp | C/T | 0.465473 | 0.126772 | intron-variant | ASB7 | GRCh38.p7 | 15:100613752 | CTTCTGCCAGCCTTA[C/T]TTTAAAAAAAGTTAC | 140460 |
rs8042399 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ASB7 | GRCh38.p7 | 15:100627726 | GGTGGCTGAAGGGTG[A/G]GAGAAGTGAAAAGAA | 140460 |
rs9672619 | snp | A/G | 0.0279526 | 0.114869 | downstream-variant-500B, intron-variant | ASB7 | GRCh38.p7 | 15:100630560 | GTATTTAGGGATACC[A/G]CTCGTGGAAGTTAAG | 140460 |
rs9788654 | snp | A/G | 0.376791 | 0.215463 | intron-variant | ASB7 | GRCh38.p7 | 15:100620534 | TGCATATAATAGCAC[A/G]TCTGTACAAACCCTG | 140460 |
rs10083594 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ASB7 | GRCh38.p7 | 15:100624807 | ctgatacagaccaaa[C/T]aaagaccttggaaga | 140460 |
rs10162740 | snp | A/G | 0.411578 | 0.190768 | intron-variant | ASB7 | GRCh38.p7 | 15:100637021 | ctctcaggaaaagac[A/G]ttccaattccactta | 140460 |
rs10162923 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ASB7 | GRCh38.p7 | 15:100618241 | cctgtcttagccttc[C/T]gagtagctgggacta | 140460 |
rs10220832 | snp | C/T | 0.487432 | 0.0782705 | intron-variant | ASB7 | GRCh38.p7 | 15:100607008 | AAATACATGAATTAG[C/T]CGGGTGTGGTGGCAC | 140460 |
rs10220881 | snp | A/C | 0.487432 | 0.0782705 | intron-variant | ASB7 | GRCh38.p7 | 15:100607282 | ATTCTCATCTCTGGA[A/C]TTCCTCTGTTGTTTT | 140460 |
rs10220889 | snp | C/T | 0.486 | 0.0824865 | intron-variant | ASB7 | GRCh38.p7 | 15:100609157 | ATGTTTTATCTAGTT[C/T]GGTGTATGCATAAAG | 140460 |
rs10431863 | snp | A/G | 0.465368 | 0.126951 | intron-variant | ASB7 | GRCh38.p7 | 15:100616418 | TGTCTTGTTTAGGAA[A/G]TATACTGCAGGGTCA | 140460 |
rs10438487 | snp | C/T | 0.495708 | 0.0461266 | intron-variant | ASB7 | GRCh38.p7 | 15:100614649 | AGGCTGTAGcagggg[C/T]atccagtcttttggc | 140460 |
rs10552955 | in-del | -/AATT | 0.0399052 | 0.1355 | intron-variant | ASB7 | GRCh38.p7 | 15:100641099 | TTCTAACAGGGGAGG[-/AATT]AATTTTCTAAGATGC | 140460 |
rs10637714 | in-del | -/TTC | | | intron-variant | ASB7 | GRCh38.p7 | 15:100647019 | TGTGAAAGAATGACG[-/TTC]TTCTTGTTAAATTTT | 140460 |
rs11247228 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | ASB7 | GRCh38.p7 | 15:100611555 | cgcaatctcagctca[A/C]tgaaacctccacctc | 140460 |
rs11350952 | in-del | -/T | 0.446249 | 0.154875 | intron-variant | ASB7 | GRCh38.p7 | 15:100611820 | AAAATATATTGCTAC[-/T]TTTTTTTTTTTTTTT | 140460 |
rs11631248 | snp | A/C | 0.498754 | 0.0249289 | intron-variant | ASB7 | GRCh38.p7 | 15:100642240 | TGTGAGGATGGTAGC[A/C]TTTCTGTCAGTGCTT | 140460 |
rs11631722 | snp | C/T | 0.475877 | 0.107142 | intron-variant | ASB7 | GRCh38.p7 | 15:100611077 | TGAGACAGGGTCTTG[C/T]TCTGTATCCCAGGCT | 140460 |
rs11633584 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | LINS1, ASB7 | GRCh38.p7 | 15:100600697 | AGAAATGGAAATTTA[A/G]AAAGTTGAAATTATG | 140460 |
rs11634093 | snp | A/G | | | intron-variant | ASB7 | GRCh38.p7 | 15:100644128 | tggcacacgcctata[A/G]tcccagctactcggg | 140460 |
rs11634123 | snp | G/T | 0 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100643990 | tggcggctcatgccc[G/T]taatcccagcacttt | 140460 |
rs11634772 | snp | G/T | 0 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100636068 | tggctgccactctca[G/T]accagtcaattcaca | 140460 |
rs11637567 | snp | G/T | 0.5 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100644010 | cccagcactttggga[G/T]gctgaggcagctgga | 140460 |
rs11637849 | snp | C/T | 0 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100643989 | atggcggctcatgcc[C/T]ttaatcccagcactt | 140460 |
rs11637851 | snp | C/T | 0 | 0 | intron-variant | ASB7 | GRCh38.p7 | 15:100644000 | tgcccttaatcccag[C/T]actttgggaggctga | 140460 |
rs11852445 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | ASB7 | GRCh38.p7 | 15:100607294 | GGACTTCCTCTGTTG[C/T]TTTTTAATAGACATA | 140460 |
rs11852820 | snp | C/G | 0.476052 | 0.106772 | intron-variant | ASB7 | GRCh38.p7 | 15:100610230 | CCGGGCGCAGTGGCT[C/G]ACGCCTGTAATCCTA | 140460 |
rs11853030 | snp | C/G | 0.468047 | 0.122292 | intron-variant | ASB7 | GRCh38.p7 | 15:100605606 | TCTAAAGCCAGATAT[C/G]ATTTATATGGGCATA | 140460 |
rs11853580 | snp | A/G | 0.495782 | 0.0457324 | intron-variant | ASB7 | GRCh38.p7 | 15:100646105 | GTGGAATCTACACTT[A/G]GGCAGCAGCATAGGG | 140460 |
rs11856446 | snp | G/T | 0.474 | 0.111014 | intron-variant | ASB7 | GRCh38.p7 | 15:100604708 | AATGACTGTTCCCTG[G/T]TGAAAACTTAGGGCA | 140460 |
rs11856651 | snp | A/T | 0.47517 | 0.10862 | intron-variant | ASB7 | GRCh38.p7 | 15:100605649 | CTTTCAGCCTTCCAC[A/T]TCATAATCCCCTGAA | 140460 |