SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12221 | snp | C/T | 0.312083 | 0.242169 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714597 | CCAGGCGCCAGTATA[C/T]AGTCCTCCTCCTGCC | 8027 |
rs723790 | snp | C/T | 0.186421 | 0.24178 | intron-variant | STAM | GRCh38.p7 | 10:17683432 | GCTCACACCTATAAT[C/T]CCAGCATTTTGGGAG | 8027 |
rs723791 | snp | A/C | 0.175254 | 0.238565 | intron-variant | STAM | GRCh38.p7 | 10:17683367 | TGGGACCAGCCTGGG[A/C]AACACTGTGAAACCC | 8027 |
rs723792 | snp | A/G | 0.176861 | 0.239062 | intron-variant | STAM | GRCh38.p7 | 10:17683307 | GCCAGAAATGGTCCC[A/G]GCTCCTATGGGCGCA | 8027 |
rs942775 | snp | C/T | 0.145978 | 0.227331 | intron-variant | STAM | GRCh38.p7 | 10:17709047 | TCTGGCTAATAAATA[C/T]CTGTGGTCAGCGTCA | 8027 |
rs1007264 | snp | A/G | 0.29432 | 0.24604 | intron-variant | STAM | GRCh38.p7 | 10:17668275 | AGTTTTAGGAAAGAG[A/G]GAGAGTGGTTTGGAA | 8027 |
rs1061162 | snp | A/G | 0.136166 | 0.22258 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715297 | CTTCAAGAAAACAAA[A/G]TTGTTAGCGTATTTA | 8027 |
rs1359506 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17699188 | TGGAAAGATTAAAAA[C/G]TTTTGTAAAAGAGAA | 8027 |
rs1359507 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17698794 | CTAACAGCTCTTGAC[A/G]CGCAAGTTTGCAACC | 8027 |
rs1801675 | snp | A/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715113 | TGTTATGTACATATA[A/T]TGATATGTAACTGCA | 8027 |
rs1937348 | snp | A/G | 0.44858 | 0.151875 | intron-variant | STAM | GRCh38.p7 | 10:17648683 | CTTGCCACTGACTAT[A/G]AGAGATAACAATGAC | 8027 |
rs1937349 | snp | A/T | 0.130008 | 0.219321 | intron-variant | STAM | GRCh38.p7 | 10:17653395 | TTTTGATAAAACAGG[A/T]TAAAAACTCTGAACA | 8027 |
rs1977342 | snp | A/G | 0.296364 | 0.245663 | intron-variant | STAM | GRCh38.p7 | 10:17707175 | tgatccacccgcctc[A/G]gcctcccaacgtgct | 8027 |
rs2001832 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17675700 | ttcttgttcactact[G/T]tattcctaaagcctt | 8027 |
rs2031514 | snp | A/G | 0.496968 | 0.0388195 | intron-variant | STAM | GRCh38.p7 | 10:17676700 | TTTCGCGAGTGAAAG[A/G]TGGTGTTAACTGGAC | 8027 |
rs2031515 | snp | C/T | 0.12932 | 0.218944 | intron-variant | STAM | GRCh38.p7 | 10:17676495 | TTCCAATGTCTTTTT[C/T]TCAAATCACAGACCA | 8027 |
rs2182158 | snp | C/T | 0.136506 | 0.222754 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689273 | ACAGACTGTAATGAG[C/T]GATGTGAAACCATGA | 8027 |
rs2243617 | snp | A/G | 0.346147 | 0.230772 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643728 | GACTTCATCCGAGCA[A/G]GTTTGTCACCTCACG | 8027 |
rs2244877 | snp | A/G | 0.127599 | 0.217986 | intron-variant | STAM | GRCh38.p7 | 10:17654793 | ATATTTTTCAAAAAA[A/G]TCTAGGTCTTGTTGT | 8027 |
rs2244878 | snp | C/G | 0.127599 | 0.217986 | intron-variant | STAM | GRCh38.p7 | 10:17654795 | ATTTTTCAAAAAAGT[C/G]TAGGTCTTGTTGTTT | 8027 |
rs2246058 | snp | C/T | 0.128632 | 0.218563 | intron-variant | STAM | GRCh38.p7 | 10:17677951 | AGTAAAAACTTTTAT[C/T]GGGCAATTTGAACTC | 8027 |
rs2251596 | snp | C/T | 0.473174 | 0.112665 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642399 | TGTACTATGATTTAA[C/T]TGACCAGTGTAAATT | 8027 |
rs2251710 | snp | A/T | 0.3748 | 0.216622 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643342 | ATTATTCTCTGTGTG[A/T]TGGAGAAGTTTTAAG | 8027 |
rs2253965 | snp | C/T | 0.258843 | 0.249844 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697804 | GCATATCAACCTATA[C/T]ATATAAGCTCTTTAA | 8027 |
rs2255065 | snp | A/G | 0.137187 | 0.223099 | intron-variant | STAM | GRCh38.p7 | 10:17647389 | ggatttcaggacacc[A/G]aactttttctcattt | 8027 |
rs2255153 | snp | A/C | 0.137527 | 0.223271 | intron-variant | STAM | GRCh38.p7 | 10:17647578 | cctgggactgaatcc[A/C]agcagtgtggcccca | 8027 |
rs2255426 | snp | G/T | 0.467337 | 0.123551 | intron-variant | STAM | GRCh38.p7 | 10:17650311 | TGTATAATGGATATT[G/T]CTATCCCTATTTACC | 8027 |
rs2255657 | snp | C/G | 0.47517 | 0.10862 | intron-variant | STAM | GRCh38.p7 | 10:17651913 | TTTCTCAAAATTTAT[C/G]ACTGTCAAAGATCTG | 8027 |
rs2255760 | snp | C/T | 0.475081 | 0.108804 | intron-variant | STAM | GRCh38.p7 | 10:17652606 | ACCTGCCACCTTATT[C/T]AAAAACATAATAGCT | 8027 |
rs2264643 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17656111 | agagacgggtttcac[C/T]gtgttagccaggatg | 8027 |
rs2272143 | snp | A/T | 0.142358 | 0.22564 | intron-variant | STAM | GRCh38.p7 | 10:17709003 | TGTTACAGCTGTTTA[A/T]GTGCCCCCAGTTATC | 8027 |
rs2272146 | snp | C/T | 0.185788 | 0.241613 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696485 | ATTGTCAGCTTCAGA[C/T]GGTTCACAGGCTCCA | 8027 |
rs2280583 | snp | C/T | 0.0693013 | 0.172766 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643818 | GGGAATACAAGGTTA[C/T]GATAACCGAGAGAGC | 8027 |
rs2357291 | snp | A/G | 0.173643 | 0.238054 | intron-variant | STAM | GRCh38.p7 | 10:17662373 | ATCCTTTCAGACCCA[A/G]TGTAGATACCACTTC | 8027 |
rs2357292 | snp | A/T | 0.472989 | 0.113031 | intron-variant | STAM | GRCh38.p7 | 10:17662634 | TACTCTAGAGGGAGA[A/T]TGCCTGGGTTCAAAT | 8027 |
rs2357293 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | STAM | GRCh38.p7 | 10:17662889 | CTGTTGAAGACTGGG[C/T]ACCAAGCTAGACCAC | 8027 |
rs2357294 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669905 | ttttttttttttttg[G/T]atttttagtagacac | 8027 |
rs2461890 | snp | C/T | 0.46754 | 0.123192 | intron-variant | STAM | GRCh38.p7 | 10:17649636 | AATGTTCTAGAAAAA[C/T]ACCAATAATTCATTA | 8027 |
rs2570276 | snp | A/C | 0.090703 | 0.192677 | | | GRCh38.p7 | 10:17702220 | ATCATTACCTTATAC[A/C]TATGAATGAATCTAA | 8027 |
rs2570277 | snp | A/G | 0.34101 | 0.232846 | | | GRCh38.p7 | 10:17709798 | TCCTCAAAGAGTTAC[A/G]TGTTAGAGATGCTTG | 8027 |
rs2570278 | snp | C/T | 0.48679 | 0.0801892 | | | GRCh38.p7 | 10:17712538 | CCAAGTACAAGAGCA[C/T]TGAATTTCCCAACAA | 8027 |
rs2570284 | snp | C/T | 0.488424 | 0.0751925 | | | GRCh38.p7 | 10:17674872 | TTAGAATTATTTTTT[C/T]CTAATGGTATTTTTC | 8027 |
rs2570285 | snp | C/G | 0.138886 | 0.22395 | | | GRCh38.p7 | 10:17678337 | aacctgggaggtgca[C/G]gttacagtgaactga | 8027 |
rs2570286 | snp | A/C | 0.130008 | 0.219321 | | | GRCh38.p7 | 10:17683712 | ttccagcatgcttat[A/C]atagcttatataaag | 8027 |
rs2570287 | snp | A/G | 0.492287 | 0.0616198 | | | GRCh38.p7 | 10:17684071 | GGCCTCATCTCTGAC[A/G]ACTGTGTGAGCGTTG | 8027 |
rs2570288 | snp | A/C | 0.130351 | 0.219509 | | | GRCh38.p7 | 10:17686518 | AGTAGCTGGGAATAC[A/C]GGCATGCGCCACCAC | 8027 |
rs2570289 | snp | A/G | 0.130694 | 0.219696 | | | GRCh38.p7 | 10:17695869 | tccatttgggctgcc[A/G]taacaaactaccgta | 8027 |
rs2688786 | snp | C/T | 0.360632 | 0.224189 | intron-variant | STAM | GRCh38.p7 | 10:17706173 | CAAGTAAAAAAATTC[C/T]GTTAAACTTTATTTT | 8027 |
rs2688787 | snp | C/T | 0.240478 | 0.249819 | intron-variant | STAM | GRCh38.p7 | 10:17703997 | CCTCTTATGTCATGC[C/T]AGAGGATTTTGCTTT | 8027 |
rs2688788 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | STAM | GRCh38.p7 | 10:17692247 | TTAAACAAGGTACTG[C/T]GATATGAGTGGTTAA | 8027 |
rs2688789 | snp | C/T | 0.485255 | 0.0845871 | intron-variant | STAM | GRCh38.p7 | 10:17691015 | AACTTCACAATTAGA[C/T]AGATTTGAACTTTTA | 8027 |
rs2688790 | snp | A/G | 0.489434 | 0.0719116 | intron-variant | STAM | GRCh38.p7 | 10:17683856 | AATATAAAATTCAAA[A/G]TACTAAGCATTCAAT | 8027 |
rs2688791 | snp | C/T | 0.425123 | 0.178415 | intron-variant | STAM | GRCh38.p7 | 10:17708636 | GTTTTTCAAAATGCC[C/T]GTTGACAGAAATAAC | 8027 |
rs2688797 | snp | G/T | 0.128976 | 0.218754 | intron-variant | STAM | GRCh38.p7 | 10:17670809 | AATTATTCCCTTAAT[G/T]TTAAGCTTATTAAGT | 8027 |
rs2764800 | snp | A/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17686514 | CCTGAGTAGCTGGGA[A/T]TACAGGCATGCGCCA | 8027 |
rs2764801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689470 | GAAGCAAAGGACATT[C/T]TTCTTCTTAAAAAAA | 8027 |
rs2764804 | snp | A/G | 0.401747 | 0.198678 | intron-variant | STAM | GRCh38.p7 | 10:17712813 | TTCTTTCTTTTTTTA[A/G]TGGGAGCAGTGCACA | 8027 |
rs2764805 | snp | A/C | 0.459574 | 0.136304 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715961 | TATTGTTTTCTTTCA[A/C]ACTGGATTTTTGGGT | 8027 |
rs3780960 | snp | A/G | 0.333722 | 0.235565 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645554 | ATATTATTTAACTGC[A/G]GAATGGAATGATGTG | 8027 |
rs3813860 | snp | C/G | 0.0912534 | 0.193131 | intron-variant | STAM | GRCh38.p7 | 10:17694586 | TAGGTTGAGTCTTTA[C/G]ACTGGTAAGAATTAC | 8027 |
rs3813861 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17694841 | AGTTTTCATGCTGTT[C/G]CAATTTTGTTAATTT | 8027 |
rs3824629 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | STAM | GRCh38.p7 | 10:17704612 | TGAGAAATGTTCCAT[G/T]TTTAATATTATCCTC | 8027 |
rs3830598 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17684423 | GTAGGAAAAAAAAAA[-/A]GGTTTGAAAATAAAA | 8027 |
rs3832661 | in-del | -/G/GG | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714959 | CAGGGGCGGGGGGGG[-/G/GG]AAGAACCTCTAAAAA | 8027 |
rs4281393 | snp | C/G | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17678850 | aatttgtctattcta[C/G]atacctcatggaagt | 8027 |
rs4400696 | snp | A/G | 0.466721 | 0.124627 | intron-variant | STAM | GRCh38.p7 | 10:17669438 | TTTCAAATTGAGTTG[A/G]CTGGGTTAAAAACAA | 8027 |
rs4551659 | snp | C/T | 0.304438 | 0.244001 | intron-variant | STAM | GRCh38.p7 | 10:17704769 | GCACTTTAAGATTTT[C/T]AGATTAATATTTTAG | 8027 |
rs4556434 | snp | A/G | 0.474272 | 0.110462 | intron-variant | STAM | GRCh38.p7 | 10:17703125 | AATTTTAAATATTGT[A/G]TAGTATTCTGTAAGC | 8027 |
rs4589180 | snp | A/G | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17648426 | aagctgggcacccta[A/G]ccagcagcAgcaacc | 8027 |
rs4747317 | snp | A/G | 0.158962 | 0.232835 | intron-variant | STAM | GRCh38.p7 | 10:17655052 | CTCTTCTTATTTTCT[A/G]AATACATCGGGAAGC | 8027 |
rs4747318 | snp | C/T | 0.123452 | 0.215605 | intron-variant | STAM | GRCh38.p7 | 10:17655342 | TTGTATTAATTCTTA[C/T]GCAAGGAATTAATCT | 8027 |
rs4747319 | snp | A/G | 0.17461 | 0.238362 | intron-variant | STAM | GRCh38.p7 | 10:17658859 | acaacatacagttgt[A/G]tgttgttttttgatt | 8027 |
rs4747320 | snp | C/G | 0.164546 | 0.234942 | intron-variant | STAM | GRCh38.p7 | 10:17666479 | ggctcactgcaagct[C/G]cgcctgccgggttca | 8027 |
rs4747321 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17674879 | ACCATTAGGAAAAAA[C/T]AATTCTAATAAACAA | 8027 |
rs4748393 | snp | A/T | 0.163236 | 0.234461 | intron-variant | STAM | GRCh38.p7 | 10:17646511 | ATACTCCTTAATGAG[A/T]GGTTGCTACATAGGA | 8027 |
rs4748394 | snp | A/G | 0.16976 | 0.236773 | intron-variant | STAM | GRCh38.p7 | 10:17653718 | ttaggcatgataagt[A/G]atctagagaaattaa | 8027 |
rs4748395 | snp | G/T | 0.137187 | 0.223099 | intron-variant | STAM | GRCh38.p7 | 10:17655348 | TAATTCTTATGCAAG[G/T]AATTAATCTGTGTGA | 8027 |
rs4748396 | snp | A/G | 0.161596 | 0.233848 | intron-variant | STAM | GRCh38.p7 | 10:17659265 | cttcccatcccttgc[A/G]tcattgctgtcattc | 8027 |
rs4748397 | snp | A/G | 0.157311 | 0.232183 | intron-variant | STAM | GRCh38.p7 | 10:17670298 | GACTTATAGAATTCT[A/G]ATGACTGTTGTGctt | 8027 |
rs4748398 | snp | C/T | 0.151668 | 0.229849 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688417 | CTACTTCTTTATAAA[C/T]GAATTGGTTTAACAT | 8027 |
rs4748399 | snp | C/T | 0.136506 | 0.222754 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689391 | GCTTTCTTCCCAAGG[C/T]ATTTCCAGTTTATCT | 8027 |
rs4748400 | snp | C/G | 0.140919 | 0.224948 | intron-variant | STAM | GRCh38.p7 | 10:17692361 | ACTGACTGATGTGTT[C/G]AAACTCAAAAGGGAA | 8027 |
rs4748401 | snp | A/G | 0.184521 | 0.241273 | intron-variant | STAM | GRCh38.p7 | 10:17694875 | TTTAAACTTTCAGTT[A/G]TGAATGAATGAATAA | 8027 |
rs4748402 | snp | C/T | 0.139225 | 0.224118 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696627 | GGCTTCTTCTTCTTT[C/T]GTAATAAAGGAAGAT | 8027 |
rs4748403 | snp | A/T | 0.114738 | 0.210248 | intron-variant | STAM | GRCh38.p7 | 10:17703589 | TTTTTTAAAAAACAT[A/T]AATACATATATACTT | 8027 |
rs4748404 | snp | A/C | 0.114738 | 0.210248 | intron-variant | STAM | GRCh38.p7 | 10:17703594 | TAAAAAACATAAATA[A/C]ATATATACTTATATA | 8027 |
rs4748405 | snp | C/G | 0.139723 | 0.224364 | intron-variant | STAM | GRCh38.p7 | 10:17705054 | GTGCATTTATGTTGT[C/G]TACCTTCTTTCCTGA | 8027 |
rs4748406 | snp | A/G | 0.115088 | 0.210473 | intron-variant | STAM | GRCh38.p7 | 10:17705276 | AAACAAGGGCTAGCT[A/G]TGTAATTCTCTTTGC | 8027 |
rs4748407 | snp | C/G | 0.183886 | 0.241099 | intron-variant | STAM | GRCh38.p7 | 10:17711159 | TCAGTTTATATATAT[C/G]TGAGAGGCTATCTCT | 8027 |
rs4748408 | snp | C/T | 0.114738 | 0.210248 | intron-variant | STAM | GRCh38.p7 | 10:17711294 | TAAAGCTACCTGTAG[C/T]GATGGTAGTATTATA | 8027 |
rs5783557 | in-del | -/T | 0.146314 | 0.227484 | intron-variant | STAM | GRCh38.p7 | 10:17675799 | TTGGTACCTATTGAA[-/T]TTTTTTTTTAACAGT | 8027 |
rs6602207 | snp | C/T | 0.462144 | 0.132269 | intron-variant | STAM | GRCh38.p7 | 10:17656879 | agaaatccaagtggg[C/T]gacttgaagagtaag | 8027 |
rs7070105 | snp | A/T | 0.32885 | 0.23724 | intron-variant | STAM | GRCh38.p7 | 10:17650917 | AAAAATACAAAAAAT[A/T]AGCCGGGCGTAGTGG | 8027 |
rs7070402 | snp | A/G | 0.16976 | 0.236773 | intron-variant | STAM | GRCh38.p7 | 10:17654105 | aagtctttgctgact[A/G]ggtagttagcatcag | 8027 |
rs7072026 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17648010 | tccttgcccttctca[C/G]tagacgacaacatga | 8027 |
rs7073509 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660214 | ATATAATTTTTTTAT[A/G]AAGAAAAATCAATGC | 8027 |
rs7073595 | snp | C/T | 0.172674 | 0.237741 | intron-variant | STAM | GRCh38.p7 | 10:17657056 | cccatcggaggcttt[C/T]ttcccttttctggtg | 8027 |
rs7075270 | snp | A/C | 0.126219 | 0.217206 | intron-variant, missense | STAM | GRCh38.p7 | 10:17713291 | ccaggggacctcatg[A/C]agcccggtgattctg | 8027 |
rs7076184 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17704697 | TGAATTCTTATAATT[A/T]TCTATCCAAACGAAG | 8027 |
rs7076634 | snp | C/T | 0.145305 | 0.227022 | intron-variant | STAM | GRCh38.p7 | 10:17673293 | ATGTTTTCCACTTAG[C/T]GAACTCAGTGGAAGA | 8027 |
rs7077009 | snp | C/T | 0.159951 | 0.233219 | intron-variant | STAM | GRCh38.p7 | 10:17664341 | TAGTAGGATTAAGTA[C/T]ACTCACATGCCCGCT | 8027 |
rs7077101 | snp | A/T | 0.466204 | 0.125522 | intron-variant | STAM | GRCh38.p7 | 10:17657196 | tggtgcctgcattca[A/T]ttaacactttaatgt | 8027 |
rs7079026 | snp | G/T | 0.473634 | 0.111748 | intron-variant | STAM | GRCh38.p7 | 10:17661501 | ATGGCATCTGTATTT[G/T]CAGCTCTTCTTACTC | 8027 |
rs7079145 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | STAM | GRCh38.p7 | 10:17652596 | TAATATGCTTAGCTA[C/T]TATGTTTTTGAATAA | 8027 |
rs7082188 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17702443 | ttgctgtggtgttta[A/C]attcctttggctata | 8027 |
rs7082861 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645072 | TTGTTTTCTGAATCA[C/G]TGGTATTAGGTACTG | 8027 |
rs7083558 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | STAM | GRCh38.p7 | 10:17692374 | TTCAAACTCAAAAGG[C/G]AAAAAGTGAACGGAG | 8027 |
rs7083803 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696066 | attcatgacttaatc[A/G]ctttccaaagtcccc | 8027 |
rs7087273 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696199 | AAGAAAATAAAGTTT[A/G]AGCTGGTTAGCTGGA | 8027 |
rs7089066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17656763 | agaaagaattcatct[A/G]aggggcgtaaggcag | 8027 |
rs7089113 | snp | A/C | 0.172674 | 0.237741 | intron-variant | STAM | GRCh38.p7 | 10:17663921 | CATATTAGGACATTC[A/C]TGGGCCCTAGGCACT | 8027 |
rs7089506 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655055 | TTCTTATTTTCTAAA[A/T]ACATCGGGAAGCCCT | 8027 |
rs7091657 | snp | C/T | 0.161924 | 0.233971 | intron-variant | STAM | GRCh38.p7 | 10:17660264 | AAAGAGGCAACTGCA[C/T]TGTGAATAGGGAAAA | 8027 |
rs7092926 | snp | G/T | 0.49998 | 0.00319482 | intron-variant | STAM | GRCh38.p7 | 10:17664114 | ACTTCCAAAATTATT[G/T]TGAGTCCTAGGCCCT | 8027 |
rs7093153 | snp | C/T | 0.204496 | 0.245824 | intron-variant | STAM | GRCh38.p7 | 10:17664461 | AACATTTGTAGTTTG[C/T]CTTTAATATTTTAAA | 8027 |
rs7095838 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | STAM | GRCh38.p7 | 10:17710909 | ATATAAAGGTACAAT[A/G]TGTAATATCTGTTTA | 8027 |
rs7096092 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | STAM | GRCh38.p7 | 10:17670191 | gaatgggatccgatg[C/T]GAGCTGATTTTTCTA | 8027 |
rs7096807 | snp | A/G | 0.153665 | 0.230694 | intron-variant | STAM | GRCh38.p7 | 10:17670744 | TAATAGTCAAATAAC[A/G]TCACTGTATATATTT | 8027 |
rs7098091 | snp | A/G | 0.172028 | 0.23753 | intron-variant | STAM | GRCh38.p7 | 10:17658432 | atgaagtagtctata[A/G]atgtcaattgtcaat | 8027 |
rs7098851 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17658965 | gtgttaatagctacc[A/G]tatttgttactgttt | 8027 |
rs7099359 | snp | A/T | 0.158962 | 0.232835 | intron-variant | STAM | GRCh38.p7 | 10:17653355 | atctcacagagttaa[A/T]tgtttgttttggtaa | 8027 |
rs7100672 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17654074 | gtcttatggagagct[G/T]tgtcttcaacctgtg | 8027 |
rs7342130 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | STAM | GRCh38.p7 | 10:17649502 | CTGACATTAATTGAT[G/T]GATTATCTTTTGTGT | 8027 |
rs7350432 | snp | G/T | 0.474453 | 0.110094 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696106 | TACCATTGCTTTGGG[G/T]GTTAGGATTTCAACC | 8027 |
rs7476478 | snp | A/G | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17703028 | aaaaaaaaaaaaaaa[A/G]aaaagaaaaGAAAAG | 8027 |
rs7899184 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17690822 | TTTTGATGTAAAGAT[A/G]GAAGTAGGCTAGCAG | 8027 |
rs7899398 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660693 | gagttagaggctgca[A/G]tgtgtgatgattaca | 8027 |
rs7899570 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17660922 | TGATGCTTTAATCAC[C/T]CTCCTTCATATTTTC | 8027 |
rs7902563 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | STAM | GRCh38.p7 | 10:17666662 | ttggcctcccaaagc[A/G]ctgggattacaggca | 8027 |
rs7903444 | snp | A/T | 0.118933 | 0.212888 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645128 | TTTGGTTTTTAATTT[A/T]ATTTTATTTTATTTT | 8027 |
rs7904112 | snp | A/G | 0.138886 | 0.22395 | intron-variant | STAM | GRCh38.p7 | 10:17691928 | CATCTGTAGAGGTCT[A/G]TTTACACTGTAGTTG | 8027 |
rs7906075 | snp | C/T | 0.128632 | 0.218563 | intron-variant | STAM | GRCh38.p7 | 10:17667112 | AATAGCGGAAGTGTT[C/T]CAGCAGAGTTAAATA | 8027 |
rs7906323 | snp | A/G | 0.128976 | 0.218754 | intron-variant | STAM | GRCh38.p7 | 10:17667163 | cagagtttcactttt[A/G]ttgcccaggctggag | 8027 |
rs7906513 | snp | A/G | 0.16028 | 0.233346 | intron-variant | STAM | GRCh38.p7 | 10:17667560 | AAtactgaatgccaa[A/G]tatcatgctttggct | 8027 |
rs7906638 | snp | A/G | 0.16028 | 0.233346 | intron-variant | STAM | GRCh38.p7 | 10:17667624 | ccgtcaatggtgcta[A/G]tattctaatggtgga | 8027 |
rs7906666 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17667677 | aacagatgatggtca[A/G]tagctaagaagctag | 8027 |
rs7907395 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17667928 | CTGAATGAGCGCAGA[C/G]CTGGGTTTCAgagtg | 8027 |
rs7908349 | snp | C/G | 0.175254 | 0.238565 | intron-variant | STAM | GRCh38.p7 | 10:17685515 | GTGATCAGTCTAAAG[C/G]ATTTATTAGGGGAAC | 8027 |
rs7912814 | snp | C/T | 0.326976 | 0.237854 | intron-variant | STAM | GRCh38.p7 | 10:17656614 | tgaatcttaattggt[C/T]atggcatatgtaatt | 8027 |
rs7913958 | snp | C/T | 0.16028 | 0.233346 | intron-variant | STAM | GRCh38.p7 | 10:17665226 | AAACCCATTTTCTGT[C/T]CTTTAAACTCACATA | 8027 |
rs7916468 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17664387 | ttatccatcatccca[A/C]actgaaaccctgtgc | 8027 |
rs7919461 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | STAM | GRCh38.p7 | 10:17691170 | TCAGAATTGAGAGTG[C/T]TTAAAGTTGTATTCT | 8027 |
rs7919471 | snp | C/T | 0.47517 | 0.10862 | intron-variant | STAM | GRCh38.p7 | 10:17691185 | TTTAAAGTTGTATTC[C/T]GTGAACACCAAAAAG | 8027 |
rs7919477 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17691202 | TGAACACCAAAAAGT[G/T]TTTTTCTTCTCAGCT | 8027 |
rs7920313 | snp | C/T | 0.139225 | 0.224118 | intron-variant | STAM | GRCh38.p7 | 10:17691850 | CTGGGAATGACAATA[C/T]ACATTCATAACTTTT | 8027 |
rs7921895 | snp | A/T | 0.128976 | 0.218754 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689026 | GCCGACCAGTACATA[A/T]GTCTTCCTTTCCCCA | 8027 |
rs9423967 | snp | C/T | 0.34101 | 0.232846 | intron-variant | STAM | GRCh38.p7 | 10:17682004 | GGCCTGTCATTTAAA[C/T]AGATCTGtttttact | 8027 |
rs9787477 | snp | A/G | 0.312104 | 0.242163 | intron-variant | STAM | GRCh38.p7 | 10:17666443 | TTTGTTGCTCAGGCT[A/G]GAGTGCAGTGGCACG | 8027 |
rs9919368 | snp | C/T | 0.314057 | 0.241654 | intron-variant | STAM | GRCh38.p7 | 10:17687292 | CCAGCCTGGCCAACA[C/T]GGTAAAACCCCGCGT | 8027 |
rs9971171 | snp | A/G | 0.213635 | 0.247341 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645776 | CTCAGTGACATAAGA[A/G]ATACAGTGATGAGCA | 8027 |
rs10218862 | snp | C/T | 0.474272 | 0.110462 | intron-variant | STAM | GRCh38.p7 | 10:17665669 | ATGTAGAATATCTAA[C/T]ACATATACATAATTA | 8027 |
rs10218865 | snp | C/T | 0.160609 | 0.233472 | intron-variant | STAM | GRCh38.p7 | 10:17665872 | ATATTCACATGATTT[C/T]TACTGCGCAATTTCC | 8027 |
rs10218868 | snp | A/C | 0.472429 | 0.114129 | intron-variant | STAM | GRCh38.p7 | 10:17665994 | CACAATGATAATAGC[A/C]GTTTTCTTTAACATG | 8027 |
rs10218900 | snp | C/G | 0.476227 | 0.106402 | intron-variant | STAM | GRCh38.p7 | 10:17707308 | CCAGCTACTTGGGAG[C/G]CTGAGGCAGGAGAAT | 8027 |
rs10219064 | snp | A/C | 0.309401 | 0.24284 | intron-variant | STAM | GRCh38.p7 | 10:17708545 | TTTCTTTAATGCTTC[A/C]GTATGGAGATAACAT | 8027 |
rs10508543 | snp | C/T | 0.114036 | 0.209795 | intron-variant | STAM | GRCh38.p7 | 10:17711942 | TTTGTTGGCAAGATA[C/T]AGTGCTATTAATTGG | 8027 |
rs10606057 | in-del | -/AA | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17651090 | AAAAAAAAAAAAAAA[-/AA]GTTCTGAAGAATCTA | 8027 |
rs10657001 | in-del | -/TATC | 0.154993 | 0.231244 | intron-variant | STAM | GRCh38.p7 | 10:17670758 | ATCACTGTATATATT[-/TATC]TATATTCACGTTCCA | 8027 |
rs10673746 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666412 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 8027 |
rs10795500 | snp | C/T | 0.326976 | 0.237854 | intron-variant | STAM | GRCh38.p7 | 10:17660641 | CTGTAGGCCCAGCCC[C/T]TCGGTAGGATGAGGT | 8027 |
rs10795501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668770 | TGCATTTAAGGTTCC[C/T]ACGTGCCTTTTCGTG | 8027 |
rs10795504 | snp | C/T | 0.299916 | 0.244966 | intron-variant | STAM | GRCh38.p7 | 10:17686181 | GTCCTGAATGTCCAT[C/T]GAGATTACAACTGTT | 8027 |
rs10795505 | snp | A/G | 0.288906 | 0.246954 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698148 | TCATAGTTATTGCCA[A/G]GGTGTCTGGTGTCAT | 8027 |
rs10795506 | snp | A/G | 0.288646 | 0.246995 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698500 | TTTTTCACTCTGGAC[A/G]ATCTAAAAGAGAAAC | 8027 |
rs10904977 | snp | C/T | 0.163564 | 0.234582 | intron-variant | STAM | GRCh38.p7 | 10:17649141 | GAATGCAGTGGCTCA[C/T]GCCAGTAACCCCTAC | 8027 |
rs10904978 | snp | C/T | 0.16976 | 0.236773 | intron-variant | STAM | GRCh38.p7 | 10:17652508 | ATTAATCAAGAACTG[C/T]AAGATAGCACTCAAC | 8027 |
rs10904982 | snp | C/T | 0.327211 | 0.237778 | intron-variant | STAM | GRCh38.p7 | 10:17661995 | GTGTGTTACATATCG[C/T]GTTCCCTTTTCTCCA | 8027 |
rs10904986 | snp | A/G | 0.338069 | 0.233974 | intron-variant | STAM | GRCh38.p7 | 10:17672391 | TCCTCTGACTGTAGA[A/G]TTGAGCTGTATCATA | 8027 |
rs10904991 | snp | A/C | 0.157311 | 0.232183 | intron-variant | STAM | GRCh38.p7 | 10:17677247 | AGTTTCATTTCAACA[A/C]CCCTTTCCCCACCAT | 8027 |
rs10904992 | snp | C/T | 0.208779 | 0.246578 | intron-variant | STAM | GRCh38.p7 | 10:17681218 | TTTTTTTTTTTTTAA[C/T]GTAGGTGCTTATAGG | 8027 |
rs10904993 | snp | A/G | 0.20111 | 0.245173 | intron-variant | STAM | GRCh38.p7 | 10:17682435 | TGTGAACATTCTTAT[A/G]AAGAGTACTGGGTAG | 8027 |
rs10904994 | snp | A/G | 0.288386 | 0.247035 | intron-variant | STAM | GRCh38.p7 | 10:17687421 | CCCCCTCTGGGAGGC[A/G]GAGGTTGCAGTGTGC | 8027 |
rs10904996 | snp | A/G | 0.304937 | 0.243889 | intron-variant | STAM | GRCh38.p7 | 10:17705813 | TAGCTCATGCCTGTA[A/G]TCTCAGCAATTTGGG | 8027 |
rs10904997 | snp | A/T | 0.304937 | 0.243889 | intron-variant | STAM | GRCh38.p7 | 10:17706285 | GGTTATGcagcagaa[A/T]cagccatcacacttt | 8027 |
rs11254699 | snp | A/G | 0.163564 | 0.234582 | intron-variant | STAM | GRCh38.p7 | 10:17649523 | TCTTTTGTGTGGAAT[A/G]TAAACTCCATTAAGA | 8027 |
rs11254700 | snp | A/G | 0.170084 | 0.236883 | intron-variant | STAM | GRCh38.p7 | 10:17652313 | TTTGATGATTTTGAG[A/G]CAGCCTCAATAAATG | 8027 |
rs11254701 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | STAM | GRCh38.p7 | 10:17654228 | TGTTATTATTATTAT[C/T]ATTATTATTTTTGAG | 8027 |
rs11254703 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17655358 | GCAAGGAATTAATCT[C/G]TGTGAATAACCTGCT | 8027 |
rs11254704 | snp | A/T | 0.172351 | 0.237636 | intron-variant | STAM | GRCh38.p7 | 10:17656567 | TTGGAGGGTAACGGT[A/T]CAAATGTTGAATCAG | 8027 |
rs11254705 | snp | A/C | 0.17332 | 0.23795 | intron-variant | STAM | GRCh38.p7 | 10:17656857 | AAGAAAGGAAAGTGC[A/C]CTTGGAAGAAATCCA | 8027 |
rs11254707 | snp | C/G/T | 0.00953873 | 0.0683987 | intron-variant | STAM | GRCh38.p7 | 10:17658738 | ATGATCTGCCCACTT[C/G/T]GGCCTCCCAAAGTGT | 8027 |
rs11254708 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | STAM | GRCh38.p7 | 10:17661480 | CTTCCAGCTGTCTTT[A/C]TGTAGATGGCATCTG | 8027 |
rs11254709 | snp | C/T | 0.172997 | 0.237846 | intron-variant | STAM | GRCh38.p7 | 10:17661613 | TCCTGTCTCTTTTTG[C/T]TTTAAACCTACTTTC | 8027 |
rs11254710 | snp | C/T | 0.172997 | 0.237846 | intron-variant | STAM | GRCh38.p7 | 10:17661629 | TTTAAACCTACTTTC[C/T]TTCAGTTTTTCCATT | 8027 |
rs11254711 | snp | C/T | 0.17332 | 0.23795 | intron-variant | STAM | GRCh38.p7 | 10:17661695 | AAACTTGAGTCACCT[C/T]CACATTTATTACTCA | 8027 |
rs11254712 | snp | C/T | 0.172997 | 0.237846 | intron-variant | STAM | GRCh38.p7 | 10:17661784 | TCAAGTTTTTGAGCA[C/T]AGCCAAATGGTGCAG | 8027 |
rs11254713 | snp | A/G | 0.172674 | 0.237741 | intron-variant | STAM | GRCh38.p7 | 10:17663453 | ATACTAAGTCTATGA[A/G]TTTACTTAGGAAATA | 8027 |
rs11254715 | snp | C/G | 0.321292 | 0.23962 | intron-variant | STAM | GRCh38.p7 | 10:17665100 | AGGGGGAGAAAAGAG[C/G]TATTATTGTGAAGTT | 8027 |
rs11254716 | snp | C/T | 0.148661 | 0.22854 | intron-variant | STAM | GRCh38.p7 | 10:17667229 | CCTCCCAAGTTCAAG[C/T]GATTCTCCTGTCTCA | 8027 |
rs11254717 | snp | C/T | 0.16028 | 0.233346 | intron-variant | STAM | GRCh38.p7 | 10:17668488 | ACACTTTGTTTTGTA[C/T]AGGTCAATGGGTTTT | 8027 |
rs11254720 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | STAM | GRCh38.p7 | 10:17671986 | TTCCTGTCACTGCTC[A/G]GCATATGGTTTTTAT | 8027 |
rs11254721 | snp | A/G | 0.313082 | 0.241911 | intron-variant | STAM | GRCh38.p7 | 10:17677873 | AAAAAGGATTTTTTT[A/G]TATTTATTACAGTGC | 8027 |
rs11254723 | snp | A/C | 0.271972 | 0.249033 | intron-variant | STAM | GRCh38.p7 | 10:17682123 | TAAGTATCACCCCAA[A/C]CAAGATAGCATTTAA | 8027 |
rs11254724 | snp | A/G | 0.144176 | 0.226498 | intron-variant | STAM | GRCh38.p7 | 10:17684649 | GATGTATTATTAAGT[A/G]ATTTTTACTTTTCTC | 8027 |
rs11254727 | snp | A/G | 0.0513262 | 0.151752 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689389 | GTGCTTTCTTCCCAA[A/G]GCATTTCCAGTTTAT | 8027 |
rs11254734 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698402 | CAAGGATCTCATGTA[A/G]ATCCTGGAGCCATTT | 8027 |
rs11254735 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700003 | AGAGAAAATTAAGAA[A/G]TCCAATTTCATAAAG | 8027 |
rs11254736 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17700348 | GTTTTGCTTTAAGAA[A/G]AAATTGATTACTTGA | 8027 |
rs11254737 | snp | A/C | 0.478932 | 0.10045 | intron-variant | STAM | GRCh38.p7 | 10:17700770 | TTCCCAGCATACTCA[A/C]CAAGGATATTAAGAT | 8027 |
rs11254738 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17704137 | ttgcactgttgtcca[A/G]actgaagtgcagtgg | 8027 |
rs11254739 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706730 | TACTTAAGAACCTTA[A/G]TTCTTCATCAGGTTG | 8027 |
rs11254740 | snp | A/G | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17707003 | CCCTGCTTTACATGA[A/G]AATGCATGCAATGCA | 8027 |
rs11254742 | snp | C/G | 0.0788843 | 0.182262 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717216 | AAACTACAAAAATTA[C/G]CTGGGCGTGGTGGCA | 8027 |
rs11307472 | in-del | -/T | 0.17289 | 0.237811 | intron-variant | STAM | GRCh38.p7 | 10:17663289 | TTTAAAAATATTTTT[-/T]GTCTTTTTGTTTTTA | 8027 |
rs11313482 | in-del | -/A | 0.142609 | 0.225759 | intron-variant | STAM | GRCh38.p7 | 10:17652248 | TATATCCTTCTGATT[-/A]AAAAAAAAATACTTG | 8027 |
rs11338233 | in-del | -/A | 0.492287 | 0.0616198 | intron-variant | STAM | GRCh38.p7 | 10:17687501 | CTCAAAAAACAAACC[-/A]AAAAAAAAGAAAAGA | 8027 |
rs11419676 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17705109 | CTATAACTGCCTTTT[-/A]AAAAAAAAAATATTG | 8027 |
rs11591730 | snp | A/G | 0.172028 | 0.23753 | intron-variant | STAM | GRCh38.p7 | 10:17713026 | ACCGTTCTTGTCAAG[A/G]ACCCTGGTGATGCCC | 8027 |
rs11591757 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17672345 | GAAAAGAGAATTGCA[A/G]GAATGCAAAATTGCT | 8027 |
rs11591804 | snp | A/C | 0.0402882 | 0.136092 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642578 | TTGTCCAATCACTCA[A/C]TGTGGGACATTTAAT | 8027 |
rs11591978 | snp | C/T | 0.138886 | 0.22395 | intron-variant | STAM | GRCh38.p7 | 10:17690463 | CACCTACAAGAAATA[C/T]ATATAAAGTAAAATA | 8027 |
rs11592438 | snp | G/T | 0.161924 | 0.233971 | intron-variant | STAM | GRCh38.p7 | 10:17657593 | gaacccatctgggcc[G/T]gtgctttctgtttta | 8027 |
rs11593203 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | STAM | GRCh38.p7 | 10:17685209 | ATATCTAATTAAATA[A/G]TATCAGTCTATTTTA | 8027 |
rs11593224 | snp | A/G | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17692339 | GACAGTGATATTTTA[A/G]CTGATTACTGACTGA | 8027 |
rs11593242 | snp | A/T | 0.168785 | 0.236441 | intron-variant | STAM | GRCh38.p7 | 10:17655346 | ATTAATTCTTATGCA[A/T]GGAATTAATCTGTGT | 8027 |
rs11593510 | snp | C/T | 0.137527 | 0.223271 | intron-variant | STAM | GRCh38.p7 | 10:17699488 | ACTGTTATGTTAAAT[C/T]GTTTTTAAAGATTGC | 8027 |
rs11594486 | snp | A/C | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687833 | AATGCTTTAATTTGA[A/C]GTGAGATATATATGA | 8027 |
rs11595520 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | STAM | GRCh38.p7 | 10:17699691 | GCTCTCTAAACGCCT[A/G]CGTGGCACGCCAGAT | 8027 |
rs11595540 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17672006 | ATGGTTTTTATGATA[C/T]TAAAAAGTACTTTTC | 8027 |
rs11595692 | snp | A/G | 0.0622301 | 0.165053 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717269 | tcaggaggctgaggc[A/G]agagaattgcttgaa | 8027 |
rs11595824 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | STAM | GRCh38.p7 | 10:17677129 | CTCTGTCCTTTTAAT[G/T]GTTCAGTAGCCAATT | 8027 |
rs11596639 | snp | G/T | 0.0644693 | 0.167566 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713936 | cgcagtcctgccggt[G/T]atcttagctgctctc | 8027 |
rs11597115 | snp | C/T | 0.172997 | 0.237846 | intron-variant | STAM | GRCh38.p7 | 10:17679317 | ctccctaattgctag[C/T]gatgttgagcatttg | 8027 |
rs11597146 | snp | C/G | 0.172674 | 0.237741 | intron-variant | STAM | GRCh38.p7 | 10:17679502 | atattttctcccatt[C/G]tgtgggttgactttt | 8027 |
rs11598400 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17672267 | CATTTGTAAATAATA[C/T]AGTGACATTGTTGAA | 8027 |
rs11598870 | snp | A/G | 0.172674 | 0.237741 | intron-variant | STAM | GRCh38.p7 | 10:17657223 | atgtttaacacttgt[A/G]gactgttaggagctt | 8027 |
rs11599751 | snp | A/C/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17653603 | agtggatcaaaactt[A/C/G]tagaggaaaaaatat | 8027 |
rs11812612 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686123 | TCCTGCTTTATGCAG[G/T]TAATATTTATTTTCT | 8027 |
rs11813306 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687965 | CTTTACTATTTAAAA[C/T]GTCTGTATTAAATCA | 8027 |
rs11813361 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17691458 | gggaggcggagcttg[C/G]agtgagccaagatct | 8027 |
rs11813888 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17692207 | gatttgaactcatgt[C/T]tgtctgactccacaa | 8027 |
rs11813893 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17692161 | aggctaatttgccca[G/T]tgtcatccagctaga | 8027 |
rs11814188 | snp | A/G | 0.16976 | 0.236773 | intron-variant | STAM | GRCh38.p7 | 10:17650958 | tagtcccagctactc[A/G]ggaggctgaggcagg | 8027 |
rs11814206 | snp | A/G | 0.16976 | 0.236773 | intron-variant | STAM | GRCh38.p7 | 10:17651035 | ACACCACTGCATTCC[A/G]GCCTTGGTGACAGAG | 8027 |
rs11817967 | snp | C/T | 0.170733 | 0.237101 | intron-variant | STAM | GRCh38.p7 | 10:17650759 | atgtacgcgtggccc[C/T]tccgtttaaaaTATT | 8027 |
rs12049670 | snp | A/G | 0.311859 | 0.242226 | intron-variant | STAM | GRCh38.p7 | 10:17680379 | ccaggccccctggca[A/G]ccaccattctacttt | 8027 |
rs12241101 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17650544 | TGACTTCTGTAGTTG[C/T]AATTTTCTACATTCT | 8027 |
rs12243199 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17660617 | AAGgccaggtgcagt[A/G]gcttgcacctgtagg | 8027 |
rs12247311 | snp | C/T | 0.16976 | 0.236773 | intron-variant | STAM | GRCh38.p7 | 10:17653471 | ATACACACTGATGTA[C/T]TTGGAGGGTGATGAA | 8027 |
rs12247383 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | STAM | GRCh38.p7 | 10:17685614 | tgtgtttagcaacat[A/C]cttgatcttttagtg | 8027 |
rs12248781 | snp | C/T | 0.172674 | 0.237741 | intron-variant | STAM | GRCh38.p7 | 10:17659560 | ttcagcctcaacctc[C/T]tgggctcaagtgatc | 8027 |
rs12250033 | snp | A/G | 0.170084 | 0.236883 | intron-variant | STAM | GRCh38.p7 | 10:17651536 | AACTTGTATTCTTTG[A/G]TTCTTCTGTCCCTAT | 8027 |
rs12253673 | snp | C/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716255 | TAAGACTGTTGTAAT[C/G]AGGTAGCTTGTTTAT | 8027 |
rs12254619 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17667757 | gTTACGTTTATGCTA[G/T]AATTTTAATGTTGAA | 8027 |
rs12256100 | snp | A/G | 0.168581 | 0.23637 | intron-variant | STAM | GRCh38.p7 | 10:17654226 | ATTGTTATTATTATT[A/G]TTATTATTATTTTTG | 8027 |
rs12258385 | snp | C/T | 0.161924 | 0.233971 | intron-variant | STAM | GRCh38.p7 | 10:17648239 | gattgtaaaatgcac[C/T]gatcagtgctctgta | 8027 |
rs12260780 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17670735 | TTTGTTAAATAATAG[C/T]CAAATAACATCACTG | 8027 |
rs12261407 | snp | A/G | 0.298144 | 0.245321 | intron-variant | STAM | GRCh38.p7 | 10:17674737 | TGTCACCTCTTGAAG[A/G]GAAATGGTAAGTTCA | 8027 |
rs12262407 | snp | C/T | 0.161596 | 0.233848 | intron-variant | STAM | GRCh38.p7 | 10:17656074 | CCAAGGTGGGTGAGT[C/T]ACCAGGTCAGGAGAT | 8027 |
rs12262555 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17650168 | ATGTCACATTCTCCT[A/G]AAGTGTGATATGATA | 8027 |
rs12264961 | snp | A/C | 0.170084 | 0.236883 | intron-variant | STAM | GRCh38.p7 | 10:17651873 | ATGTGATGCGAAGTC[A/C]TCCTGTCAGCATTTC | 8027 |
rs12355248 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706509 | tcagcctcctgagta[A/G]ctgggactacaggcg | 8027 |
rs12360258 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716313 | TAGCCAGTAATCTTA[A/C]GGGTGACTAATTTCA | 8027 |
rs12411333 | snp | A/G | 0.289165 | 0.246913 | intron-variant | STAM | GRCh38.p7 | 10:17699412 | TAAAAATATAGAAAG[A/G]AAGTTTGTTTAGTAG | 8027 |
rs12412944 | snp | A/G | 0.0221055 | 0.102782 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696892 | TTTTCCAGCCTGCCA[A/G]TAAATGATGTTTTCT | 8027 |
rs12413908 | snp | A/G | 0.100944 | 0.200705 | intron-variant | STAM | GRCh38.p7 | 10:17653773 | ctttatgcaaattca[A/G]tgccattttatatta | 8027 |
rs12414802 | snp | A/G | 0.105569 | 0.204058 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643486 | GCTCAGTCTAGGGAG[A/G]CTATCTTGGGCTGTG | 8027 |
rs12761922 | snp | A/G | 0.365232 | 0.22186 | intron-variant | STAM | GRCh38.p7 | 10:17650451 | AAATTTTTCTTCTCA[A/G]TTATGCTTTTTGTCT | 8027 |
rs12762500 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17650677 | tagcttccagctgtt[C/T]ttccctgcttccagt | 8027 |
rs12763500 | snp | A/G | 0.122064 | 0.214785 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689758 | GTTCTTGTTAACTCA[A/G]AACTTGGTTTGACCA | 8027 |
rs12766444 | snp | A/G | 0.357451 | 0.225731 | intron-variant | STAM | GRCh38.p7 | 10:17654834 | TATTTGGAACTCTTG[A/G]CATTCTGATGTTTCT | 8027 |
rs12766551 | snp | C/T | 0.21845 | 0.248001 | intron-variant | STAM | GRCh38.p7 | 10:17656280 | gcctgggtgacagag[C/T]gagactccgtcttaa | 8027 |
rs12769584 | snp | G/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17665556 | ATTGACTACTTATTG[G/T]ATCCTGTCAGTCTTA | 8027 |
rs12771930 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17669805 | caggttcacaccgtt[A/C]tcctgcctcagcctc | 8027 |
rs12772472 | snp | C/T | 0.118933 | 0.212888 | intron-variant | STAM | GRCh38.p7 | 10:17648462 | gggtccccttccatg[C/T]tgtggaagctttgtt | 8027 |
rs12772669 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687175 | TATACATCAACCATA[A/G]AGAGTTATGTTATTT | 8027 |
rs12774316 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17687173 | GTTATACATCAACCA[A/T]AAAGAGTTATGTTAT | 8027 |
rs12774320 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17664812 | TTATTGCTATTTGGT[A/G]TTAGCCTGAAATTTT | 8027 |
rs12781245 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667268 | agtagctgggattac[A/G]ggtgaacgccaccat | 8027 |
rs12781430 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667353 | ggccttgaacccctc[A/G]ccttgtgatctgccc | 8027 |
rs12782461 | snp | C/T | 0.232067 | 0.249356 | intron-variant | STAM | GRCh38.p7 | 10:17683410 | caagccatctgccca[C/T]ctcggcctcccaaaa | 8027 |
rs12782904 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667264 | cctaagtagctggga[G/T]tacaggtgaacgcca | 8027 |
rs12783080 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667326 | catggggtttcaacg[G/T]attggtcaggtggcc | 8027 |
rs12783089 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17667337 | aacgtattggtcagg[C/T]ggccttgaacccctc | 8027 |
rs17141457 | snp | C/T | 0.135933 | 0.222461 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644335 | CACCTCGGCACGCAG[C/T]GGAGATGCCTCTTTT | 8027 |
rs17141484 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | STAM | GRCh38.p7 | 10:17676068 | TTGCACATTTGCCCT[A/G]AGAGCTTCAAGTTCT | 8027 |
rs17141513 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698459 | AGCAATGCAGCTTCA[A/G]TATGAGTTTTCTAGT | 8027 |
rs17141515 | snp | C/T | 0.24449 | 0.249939 | intron-variant | STAM | GRCh38.p7 | 10:17699672 | CTCCACTGGCATGGA[C/T]GGCGCTCTCTAAACG | 8027 |
rs17141516 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | STAM | GRCh38.p7 | 10:17700881 | CATTAAATTACTTCT[A/T]CATAAATCATTGCAT | 8027 |
rs17141517 | snp | A/C | 0.121717 | 0.214577 | intron-variant | STAM | GRCh38.p7 | 10:17704302 | TACATGGGACACTGA[A/C]AACATAAAAGCAAAA | 8027 |
rs17141524 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | STAM | GRCh38.p7 | 10:17706127 | ATTTGGAATAGCTGT[G/T]TGAAACTTTCTAAAA | 8027 |
rs17141543 | snp | A/G | 0.114738 | 0.210248 | intron-variant | STAM | GRCh38.p7 | 10:17709590 | CTTTAATGGGACTCT[A/G]AGCTGAAATCTTTTC | 8027 |
rs17141551 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | STAM | GRCh38.p7 | 10:17711328 | TGATAATAAGTGACA[A/G]TTACTGTTAGTATTT | 8027 |
rs17141555 | snp | C/T | 0.116138 | 0.211142 | intron-variant | STAM | GRCh38.p7 | 10:17711871 | GCGTAGATGGATTCA[C/T]AGGGGCAAGATTAGA | 8027 |
rs17141568 | snp | C/T | 0.163236 | 0.234461 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715863 | CTTTAACACATTGTA[C/T]CCTTTAATTCTTCAT | 8027 |
rs17379193 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | STAM | GRCh38.p7 | 10:17681842 | CTGTGAATGTTTTGA[A/G]CACTGAATGAGTCCT | 8027 |
rs17379487 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | STAM | GRCh38.p7 | 10:17701319 | CTACTCAAACTTATT[A/G]CCATGTTTTAAAAAT | 8027 |
rs17379922 | snp | A/G | 0.17138 | 0.237316 | intron-variant | STAM | GRCh38.p7 | 10:17711045 | GTTAGAAATTTCCTT[A/G]CTAGAGGTGTCCTGC | 8027 |
rs17463996 | snp | C/T | 0.175897 | 0.238765 | intron-variant | STAM | GRCh38.p7 | 10:17683940 | AGAAGTGGTTACATT[C/T]GTCTGTGGCTTATGT | 8027 |
rs17464580 | snp | G/T | 0.0889988 | 0.191255 | intron-variant | STAM | GRCh38.p7 | 10:17708969 | AATTTTACTGTTGAT[G/T]CTTGTTTGGAGTTAG | 8027 |
rs17464684 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | STAM | GRCh38.p7 | 10:17710746 | TAGCACACAGTTTTA[C/T]ACTGGCTAGGAACTC | 8027 |
rs17852767 | snp | G/T | | | missense, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696845 | AATTTTGTGACTGCA[G/T]ATCTCACTGCTGAAC | 8027 |
rs33989873 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17705119 | CTTTTAAAAAAAAAA[-/A]TATTGTGGAGGAACC | 8027 |
rs34026243 | in-del | -/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698209 | TTTCAATGATGTTTT[-/G]CTATGTCTGTGAGAA | 8027 |
rs34047773 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17675808 | ATTGAATTTTTTTTT[-/T]AACAGTGACTCTCTA | 8027 |
rs34083165 | in-del | -/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715278 | ATTATACTATCCTTT[-/T]AAACTTCAAGAAAAC | 8027 |
rs34084574 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17674607 | TCCAGGAGACCCAAA[-/A]TGTACTCCACATGGC | 8027 |
rs34089222 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17682708 | GCACATGAAAAAAAA[-/A]TGTGTATAATGCCAT | 8027 |
rs34127580 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673810 | AAGCAGGCACTCCCT[-/T]AAGCGTTAACTATTA | 8027 |
rs34202904 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17646680 | CTCTTCTCACAATCC[-/C]TTGTATTGAAATATT | 8027 |
rs34205068 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17682995 | GTCTCTCTTTATCCC[-/C]TGTTAGTATTCCTTG | 8027 |
rs34217710 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706851 | AACTCTCTTAAATAT[-/G]CTAATGAACTTCTAG | 8027 |
rs34222350 | snp | A/C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656421 | TTGACTTTTAACTTC[A/C/T]CTGTAGGTTGGTCTG | 8027 |
rs34283260 | in-del | -/AT | | | intron-variant | STAM | GRCh38.p7 | 10:17676910 | CATATATATATATAT[-/AT]AAAAGTTCAGTATTA | 8027 |
rs34286916 | in-del | -/T | 0.441926 | 0.160201 | intron-variant | STAM | GRCh38.p7 | 10:17678261 | CTTCATGTGGTGTAA[-/T]TTTTTTTTTGGAAGA | 8027 |
rs34315252 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17672105 | ATCTTGACTCCTTTT[-/T]CCAACAATAGCTTTA | 8027 |
rs34365643 | snp | A/C | 0.127254 | 0.217792 | intron-variant | STAM | GRCh38.p7 | 10:17712150 | GGTATTTAGTATGTT[A/C]CAAGCACTGTGCTGT | 8027 |
rs34413104 | in-del | -/C | | | frameshift-variant | STAM | GRCh38.p7 | 10:17700267 | GAGCCGGAACCAGCC[-/C]TTTATTGATGAAGTA | 8027 |
rs34558527 | in-del | -/A | 0.375 | 0.216506 | intron-variant | STAM | GRCh38.p7 | 10:17656314 | AAAAAAAAAAAAAAA[-/A]GATAGTTTCAGATAG | 8027 |
rs34561235 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17700793 | ATTAAGATTGTTTGC[-/A]CATGACTGAGGAAGG | 8027 |
rs34651006 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17702947 | GGGAGGCGGAAGGTC[-/C]GTAGTGAGCCAAGAT | 8027 |
rs34754639 | snp | A/C | 0.128288 | 0.218372 | intron-variant | STAM | GRCh38.p7 | 10:17670453 | CTGTGCTGTGTGCTT[A/C]GGTGCTTGTATGAGC | 8027 |
rs34802486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17655880 | AAGACTGGTTACCCT[C/T]TGCTTCTGTACAGCT | 8027 |
rs34875696 | snp | A/G | 0.234401 | 0.249513 | intron-variant | STAM | GRCh38.p7 | 10:17684574 | TTTCCCTACTTTATC[A/G]TAGTCTCCCTTTTTA | 8027 |
rs34897638 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681215 | TTTTTTTTTTTTTTT[-/T]AATGTAGGTGCTTAT | 8027 |
rs34935247 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688642 | AATTTTTTTTTTTTT[-/T]AAATAGAGGTGGGTT | 8027 |
rs34941363 | in-del | -/C | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17661911 | GGTCCCATCCATCCC[-/C]TTTGTTGTATTTACA | 8027 |
rs34999598 | in-del | -/T/TT | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17667143 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTTTCAC | 8027 |
rs35030917 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17705906 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCTGGGG | 8027 |
rs35052129 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17705195 | ATTTGTCCTTTTTTT[-/T]AAAGTGAGGATTTGA | 8027 |
rs35059702 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17677969 | AAAGTTTTTACTTTT[-/T]ATAAATACATATATA | 8027 |
rs35234918 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17672625 | CCTGTATGCAAGCCA[G/T]CTTCTTCAGCTGTTG | 8027 |
rs35277183 | snp | G/T | 0.254664 | 0.249956 | intron-variant | STAM | GRCh38.p7 | 10:17701228 | TGCATATAAAGAAAA[G/T]ATTAAAACTGGCTAC | 8027 |
rs35309388 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17657149 | ACTCAGTGCCTGAGA[-/A]TTTTATTGGAGCCCC | 8027 |
rs35331260 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17685883 | TATGTGAGTTTCCCC[-/C]AGTAAAAATTTGTGC | 8027 |
rs35363298 | in-del | -/T | | | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17695909 | TTTATAAACAACAGG[-/T]AATTTATTTCTCACA | 8027 |
rs35482541 | snp | A/G | 0.365646 | 0.221644 | intron-variant | STAM | GRCh38.p7 | 10:17655488 | TTATTTTAGTTGTCC[A/G]GTGGTAGTGACTAAC | 8027 |
rs35796286 | in-del | -/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17703345 | GTTTTTTTTTTTTTT[-/T]AGCATACTTATGTCA | 8027 |
rs35915559 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17659357 | ATACATTGTTGCTGT[-/G]TATTATTTAGAATAA | 8027 |
rs35980979 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703199 | CATTTGACCTTTTTT[-/T]GTGTGTGGTAGGCAA | 8027 |
rs35989262 | snp | C/G | 0.137187 | 0.223099 | intron-variant | STAM | GRCh38.p7 | 10:17701861 | CATATACTGGTTTTG[C/G]TATTAAGAAAGTCAT | 8027 |
rs36026223 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666981 | TTTGCTAGACTCTGT[-/T]ACAGTGCCCTATGAA | 8027 |
rs36053695 | in-del | -/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698434 | TCTTTTTTTTTTTTT[-/T]AAGTCATATAGCAAT | 8027 |
rs36055146 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667142 | AATTTTTTTTTTTTT[-/T]TGAGACAGAGTTTCA | 8027 |
rs36086698 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712664 | TACAAATGTAGGGGG[-/G]AATTCTCAGCATCTT | 8027 |
rs36122763 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670764 | GTATATATTTATATT[-/T]CACGTTCCATTATCT | 8027 |
rs41289333 | snp | C/T | 0.0184073 | 0.0941532 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660546 | TGGTCAGTCTCGCAC[C/T]GGGTAAGTATTTAGC | 8027 |
rs41289335 | snp | A/G | | | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684700 | TGTCTTCGGTCTATT[A/G]TGAGAAGAGTGAACC | 8027 |
rs41289337 | snp | A/G | 0.00376794 | 0.0432408 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696764 | AAAGCATTGTTTTTT[A/G]TTTGTCATAGTGATC | 8027 |
rs41306810 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | STAM | GRCh38.p7 | 10:17694889 | TGTGAATGAATGAAT[A/G]AACTGACAAAATGAT | 8027 |
rs41310225 | snp | G/T | 0.100588 | 0.200439 | intron-variant | STAM | GRCh38.p7 | 10:17694884 | TCAGTTGTGAATGAA[G/T]GAATAAACTGACAAA | 8027 |
rs41311220 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17694775 | GATTTAAGAGTTTGT[A/G]TTTTTTATTACCCAG | 8027 |
rs45450797 | snp | C/T | 0.0540123 | 0.155206 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643879 | AACTCAACCTGCTTT[C/T]TTTCTCCTGGCTCTC | 8027 |
rs45470994 | snp | A/T | 0.0275645 | 0.114116 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714976 | CCCCCCCGCCCCTGC[A/T]GAGGAATGAAACTAC | 8027 |
rs45489291 | snp | A/C | 0.0244538 | 0.107838 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643693 | CTCTTGGGATTCAGG[A/C]CAATTCGTTCAGCTC | 8027 |
rs45513500 | snp | C/T | 0.195837 | 0.244062 | intron-variant | STAM | GRCh38.p7 | 10:17693508 | ATGTTTTTATGACAG[C/T]TTTTTACTATACCGT | 8027 |
rs45520538 | snp | C/T | 0.114738 | 0.210248 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716521 | TTTTTGATAAATATC[C/T]GTCGGATTATAATCT | 8027 |
rs45526439 | snp | A/G | 0.114738 | 0.210248 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716548 | ATCTTTTCCACTCCA[A/G]TTTGAGTATTATGGT | 8027 |
rs45554734 | snp | C/T | 0.185472 | 0.241529 | intron-variant | STAM | GRCh38.p7 | 10:17693516 | ATGACAGTTTTTTAC[C/T]ATACCGTGTATCCAA | 8027 |
rs45563533 | snp | A/T | 0.114387 | 0.210022 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716926 | GTCTTTCAAATGACA[A/T]GACGAGGGTAGAAAT | 8027 |
rs45569833 | snp | A/G | 0.114738 | 0.210248 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716525 | TGATAAATATCTGTC[A/G]GATTATAATCTTTTC | 8027 |
rs45573444 | snp | A/G | 0.0244538 | 0.107838 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716678 | TCATGCTGAAAATCA[A/G]TGACATAGTCTCTAC | 8027 |
rs45577835 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | STAM | GRCh38.p7 | 10:17646469 | ATTTTTGCCTTTACC[A/G]AATTATTTAGCATTC | 8027 |
rs45579031 | snp | A/G | 0.0836354 | 0.186609 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644235 | GACCCTGTAGAGTCG[A/G]TCTCTGTTGCTCTTT | 8027 |
rs45607131 | snp | C/T | 0.0562307 | 0.157967 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717319 | AGTGAGACGAGATCA[C/T]GCCACTGCATTCCAG | 8027 |
rs45626436 | in-del | -/CC | 0.1609 | 0.233583 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714968 | GGTTCTTCCCCCCCC[-/CC]GCCCCTGCAGAGGAA | 8027 |
rs55662542 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17658573 | TGGAGTGCAGTGGTG[C/T]AATCTTGGTTCACTG | 8027 |
rs55813629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645102 | GATGATGTCAATTCA[A/G]TAGGTTTGCTTTTGG | 8027 |
rs56151205 | snp | G/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672838 | ATCTTACAGCAGTGT[G/T]ATTTGTGTTATGGTC | 8027 |
rs56398358 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | STAM | GRCh38.p7 | 10:17669985 | TCCGCCCATCTCGGC[C/T]TCCCAAAGTGCTGGG | 8027 |
rs56884969 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17676699 | TGTCCAGTTAACACC[A/G]TCTTTCACTCGCGAA | 8027 |
rs56977444 | snp | A/T | 0.114036 | 0.209795 | intron-variant | STAM | GRCh38.p7 | 10:17706223 | TACTAATTATGCTAA[A/T]AGTTTTTTGTTGTTG | 8027 |
rs57017755 | snp | C/G | 0.00549877 | 0.0521454 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644392 | TTGGTAAGTGTTTTT[C/G]CCTCTCCCTGCCCAT | 8027 |
rs57347245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17670732 | ATGTTTGTTAAATAA[C/T]AGTCAAATAACATCA | 8027 |
rs57550622 | in-del | -/A/AA | | | intron-variant | STAM | GRCh38.p7 | 10:17660059 | TTATCAAAAAAAAAA[-/A/AA]TCCACAAAACTAGCT | 8027 |
rs57558567 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17650699 | GCTTCCAGTTTTTCC[C/G]TAGTTATTTTCCAGA | 8027 |
rs57635058 | snp | A/G | 0.0505692 | 0.150756 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17672990 | ATAAGGAAAAGAGAG[A/G]ATGTGTCTTACAAAA | 8027 |
rs57777616 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | STAM | GRCh38.p7 | 10:17692767 | ATATATCTGAGTTCC[C/T]GAAGATAACATCCTG | 8027 |
rs57796943 | in-del | -/A | 0.0166325 | 0.0896639 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644042 | AGTCAGGCAGAGGGG[-/A]CTCCCTGTTCAGCCT | 8027 |
rs57797707 | snp | G/T | 0.0142736 | 0.0832652 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715968 | TTCTTTCACACTGGA[G/T]TTTTGGGTTGCTCTT | 8027 |
rs57874866 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697220 | AGGCGTGAGCCATCG[C/T]ACCTGGCCTAACTTT | 8027 |
rs58253160 | in-del | -/T/TA | | | intron-variant | STAM | GRCh38.p7 | 10:17676911 | ATATATATATATATA[-/T/TA]AAAGTTCAGTATTAC | 8027 |
rs58458791 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | STAM | GRCh38.p7 | 10:17680817 | AGTTCATCCCTGTTA[C/T]AGCGTATTCCATGTA | 8027 |
rs58504059 | snp | C/T | 0.114738 | 0.210248 | intron-variant | STAM | GRCh38.p7 | 10:17705880 | TAAGACCAGCCTGGG[C/T]AACATAGTGAGACTC | 8027 |
rs58750577 | snp | C/T | 0.114738 | 0.210248 | intron-variant | STAM | GRCh38.p7 | 10:17705501 | AGTACTACTTTTTGC[C/T]ATTTTTGATATTTTG | 8027 |
rs58857462 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662274 | TCCAGTGCTTTTTTT[-/T]CTACCTTAGTTTGAT | 8027 |
rs58878170 | in-del | -/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17700588 | AGTGTAGTAGTGAGA[-/T]TTTTTTTTTTTTTGA | 8027 |
rs58950607 | snp | A/T | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697798 | AAATTTTTAAAGAGC[A/T]TATATGTATAGGTTG | 8027 |
rs59313645 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678795 | CTGTCCATTTCCCCT[C/T]CTAGCCACTAGTTAC | 8027 |
rs59585445 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706396 | TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTCTCAC | 8027 |
rs59936398 | in-del | -/CA | | | intron-variant | STAM | GRCh38.p7 | 10:17701898 | AATGACTAGTTAACA[-/CA]GCTGAGATGGTTCCA | 8027 |
rs60096704 | snp | A/G | 0.149999 | 0.229128 | intron-variant | STAM | GRCh38.p7 | 10:17702785 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 8027 |
rs60168036 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17703155 | CAAACAAAACGGAAA[C/T]CATCTGTGTGTTAAT | 8027 |
rs60228856 | in-del | -/ATT | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17654237 | ATTATTATTATTATT[-/ATT]TTTGAGACGGAGGCT | 8027 |
rs60388750 | in-del | -/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715503 | TTTTGGTGCAATTAT[-/T]AGCAAATGATAATGT | 8027 |
rs60753306 | snp | A/C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700987 | TTGAGGAAAAGCTTA[A/C/T]GCTAATTTTATATTA | 8027 |
rs60772107 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | STAM | GRCh38.p7 | 10:17681060 | ATACTGTTTTACACA[A/G]CACCTGTAGCGTTTT | 8027 |
rs60838171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691344 | TAACATGGTGAAAAC[C/T]TGTCTCTACTAAAAA | 8027 |
rs60866529 | snp | C/G | 0.114036 | 0.209795 | intron-variant | STAM | GRCh38.p7 | 10:17706259 | GTTTAAAGGAAATAG[C/G]TTTTATACAGGGTTA | 8027 |
rs60907254 | snp | A/C | 0.137867 | 0.223442 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689971 | CCACAAAGGGACTTA[A/C]TCTTGTAAGAAAAGG | 8027 |
rs61132226 | snp | C/G | 0.163564 | 0.234582 | intron-variant | STAM | GRCh38.p7 | 10:17649673 | GTATTTCTATTTGCT[C/G]TTCTTTTTTCCCTCC | 8027 |
rs61214651 | in-del | -/GA | 0.5 | 0 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715389 | TGTGAGCTAAAGAGA[-/GA]TATATATATATATGT | 8027 |
rs61286866 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706370 | TCAGGGTTGAGGCCC[C/T]TTTTTTTTTTTTTTT | 8027 |
rs61299303 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17651091 | AAAAAAAAAAAAAAA[-/A]GTTCTGAAGAATCTA | 8027 |
rs61442312 | snp | C/T | 0.175576 | 0.238665 | intron-variant | STAM | GRCh38.p7 | 10:17683689 | TTCTTCATCATTATG[C/T]GGATGATTTCCAGCA | 8027 |
rs61458856 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17650866 | GTCAGCAGATCGAGA[C/T]CATCCTGGCTAACAT | 8027 |
rs61749166 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696771 | TGTTTTTTGTTTGTC[A/G]TAGTGATCCTAACTG | 8027 |
rs61842262 | snp | C/G | 0.0236746 | 0.106192 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642872 | GGTTCAAACGATTCC[C/G]AGCCTCAGCCTCCCG | 8027 |
rs61842264 | snp | C/T | 0.162909 | 0.23434 | intron-variant | STAM | GRCh38.p7 | 10:17647117 | TGATTTTTTCACTGC[C/T]GTATCCCTAGCTGTA | 8027 |
rs61842266 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | STAM | GRCh38.p7 | 10:17649775 | ATTTTTGTTTGTTTT[A/T]AAATCTTTTTTTACA | 8027 |
rs61842267 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | STAM | GRCh38.p7 | 10:17650158 | TTAAATGTTAATGTC[A/G]CATTCTCCTGAAGTG | 8027 |
rs61842268 | snp | C/T | 0.170084 | 0.236883 | intron-variant | STAM | GRCh38.p7 | 10:17651563 | CTATTTTACCTCTCC[C/T]CTAAGCTGTTTTTTC | 8027 |
rs61842289 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | STAM | GRCh38.p7 | 10:17663898 | TAGGAAATGGTAAAC[A/G]TAAGGGTCATATTAG | 8027 |
rs61842290 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | STAM | GRCh38.p7 | 10:17663909 | AAACATAAGGGTCAT[A/G]TTAGGACATTCCTGG | 8027 |
rs61842291 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17667126 | TCCAGCAGAGTTAAA[C/T]AATTTTTTTTTTTTT | 8027 |
rs61842292 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | STAM | GRCh38.p7 | 10:17667446 | TTTTTTTTAAAACGT[G/T]ATCTTGATTTCCATG | 8027 |
rs61842293 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | STAM | GRCh38.p7 | 10:17667845 | GCTGAATGCTACAAG[A/G]TAGAGAAAACTTGAT | 8027 |
rs61842294 | snp | A/G | 0.16028 | 0.233346 | intron-variant | STAM | GRCh38.p7 | 10:17668089 | AAGTTGAAAAGCCAA[A/G]GTGTTGAAAGCATCA | 8027 |
rs61842295 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17668773 | ATTTAAGGTTCCCAC[A/G]TGCCTTTTCGTGGCT | 8027 |
rs61842296 | snp | A/C | 0.157642 | 0.232314 | intron-variant | STAM | GRCh38.p7 | 10:17669412 | CCCCTTCCTACTCTC[A/C]TTAAATAAACTTTCA | 8027 |
rs61842297 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17673262 | GTTCTATTAACTACA[G/T]TTTATGAAAGGATGT | 8027 |
rs61842298 | snp | A/C | 0.145305 | 0.227022 | intron-variant | STAM | GRCh38.p7 | 10:17673673 | TTAAGGAGAAAAACC[A/C]CGCAAACCAACCCAA | 8027 |
rs61842299 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | STAM | GRCh38.p7 | 10:17674618 | CCAAATGTACTCCAC[A/G]TGGCTTCTTGTAAGT | 8027 |
rs61842300 | snp | A/G/T | 0.0268175 | 0.112843 | intron-variant | STAM | GRCh38.p7 | 10:17676122 | AAATTAGAAAGGTCT[A/G/T]TTGCAAAAGAAAGCA | 8027 |
rs61842301 | snp | A/G | 0.157311 | 0.232183 | intron-variant | STAM | GRCh38.p7 | 10:17676283 | GGTTGAGAGTGGTAT[A/G]ATGGGGCAGGAGTGG | 8027 |
rs61842302 | snp | A/G | 0.145642 | 0.227177 | intron-variant | STAM | GRCh38.p7 | 10:17676304 | GCAGGAGTGGGTATA[A/G]GGAGGATGTGATAGA | 8027 |
rs61842303 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678272 | GTAATTTTTTTTTTG[G/T]AAGACAGAGTCTCGC | 8027 |
rs61842304 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | STAM | GRCh38.p7 | 10:17680835 | CGTATTCCATGTATG[C/T]ATGTACCACATTTTG | 8027 |
rs61842305 | snp | C/T | 0.19132 | 0.247781 | intron-variant | STAM | GRCh38.p7 | 10:17681134 | CTTTGTCAACACTTA[C/T]CATTTTTTCTGTTTT | 8027 |
rs61842306 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | STAM | GRCh38.p7 | 10:17682504 | TCTGTGATTTCATTT[A/G]TTGTAAGCCTTAGAT | 8027 |
rs61842308 | snp | C/T | 0.174932 | 0.238463 | intron-variant | STAM | GRCh38.p7 | 10:17686118 | CCCTTTCCTGCTTTA[C/T]GCAGTTAATATTTAT | 8027 |
rs61842309 | snp | C/G | 0.150667 | 0.229419 | intron-variant | STAM | GRCh38.p7 | 10:17686279 | TAATAGTGCAAGCAG[C/G]CATTTCCAAAAACGA | 8027 |
rs61842334 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | STAM | GRCh38.p7 | 10:17687202 | ATTTTGGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 8027 |
rs61842335 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | STAM | GRCh38.p7 | 10:17687519 | AAAAAAGAAAAGAAA[A/G]GAAAGGAAAAAAAGT | 8027 |
rs61842337 | snp | G/T | 0.187053 | 0.241946 | intron-variant | STAM | GRCh38.p7 | 10:17692277 | AAGGTGTTATCATAA[G/T]AACAAACAAGAGAAT | 8027 |
rs61842339 | snp | A/G | 0.185472 | 0.241529 | intron-variant | STAM | GRCh38.p7 | 10:17693976 | AAGAGTTTAACTTTC[A/G]TGAATCTGGTAGGTT | 8027 |
rs61842340 | snp | A/G | 0.185472 | 0.241529 | intron-variant | STAM | GRCh38.p7 | 10:17693985 | ACTTTCATGAATCTG[A/G]TAGGTTTAAAATGAT | 8027 |
rs61842341 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17694122 | TAAATAAAATAATGA[C/T]ATGTACAAGTCTTTA | 8027 |
rs61842342 | snp | C/G | 0.191147 | 0.242974 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695661 | TTGTATGGAATTACA[C/G]ATTTATTCAGGAGGT | 8027 |
rs61842343 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696933 | TTAATGGAAGTTGAG[C/T]AAACTGAACTTTTTA | 8027 |
rs61842344 | snp | G/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697135 | GGTTTCACCATGTTG[G/T]CCAGGCTGGTCTTGA | 8027 |
rs61842345 | snp | A/T | 0.136506 | 0.222754 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697407 | GGACCGTTTCTCTAG[A/T]GTGTAGTCCCAGACT | 8027 |
rs61842346 | snp | G/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698354 | AGTTCCTGGAGAGGA[G/T]AGAATTGCTTGGAGT | 8027 |
rs61842347 | snp | A/C | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698457 | ATAGCAATGCAGCTT[A/C]AATATGAGTTTTCTA | 8027 |
rs61842348 | snp | A/G | 0.137187 | 0.223099 | intron-variant | STAM | GRCh38.p7 | 10:17700672 | TTGAAGGATTTGTGT[A/G]TTTTCCATGTTAATA | 8027 |
rs61842349 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17700953 | ATGATTCCTCCTTGT[A/G]TTGAACACTTTCTAG | 8027 |
rs61842350 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17701508 | TATATTGTTTGGCTG[C/T]TTTTGTGCTGCAGTG | 8027 |
rs61842352 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | STAM | GRCh38.p7 | 10:17709055 | ATAAATATCTGTGGT[C/T]AGCGTCATGCGGCCG | 8027 |
rs61842353 | snp | C/G | 0.0244538 | 0.107838 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716247 | TTATTTTCTAAGACT[C/G]TTGTAATCAGGTAGC | 8027 |
rs63443663 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678270 | GTGTAATTTTTTTTT[G/T]GGAAGACAGAGTCTC | 8027 |
rs66927489 | snp | C/G/T | 0.24229 | 0.251583 | intron-variant | STAM | GRCh38.p7 | 10:17664147 | GCCTACATGCATAAG[C/G/T]GTTTACAGAATTGGG | 8027 |
rs71393029 | in-del | -/A | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17680884 | CTAAAAGGCAGAAGC[-/A]ACCCAAGTGTCCACA | 8027 |
rs71495282 | snp | C/T | 0.113685 | 0.209567 | intron-variant | STAM | GRCh38.p7 | 10:17664137 | TAGGCCCTGTGCCTA[C/T]ATGCATAAGCGTTTA | 8027 |
rs71495283 | snp | C/G | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17707358 | GAGGTTGCAGTGAGC[C/G]GAGATCGTGCCATTG | 8027 |
rs71495284 | snp | A/C | 0.117188 | 0.211804 | intron-variant | STAM | GRCh38.p7 | 10:17709477 | TGTTTCTCAGGAGGC[A/C]GATGGCTGAATATGT | 8027 |
rs71507229 | in-del | -/A | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17703020 | GTAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8027 |
rs71507230 | in-del | -/TT | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17706395 | TTTTTTTTTTTTTTT[-/TT]GAGGCGGAGTCTCAC | 8027 |
rs71507231 | in-del | -/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713493 | AAGATTATTACTTTG[-/G]ATCTTCCCCACACCC | 8027 |
rs71906069 | in-del | -/ATCT | | | intron-variant | STAM | GRCh38.p7 | 10:17670759 | TCACTGTATATATTT[-/ATCT]ATATTCACGTTCCAT | 8027 |
rs72446968 | in-del | -/GA | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715388 | TTGTGAGCTAAAGAG[-/GA]ATATATATATATATG | 8027 |
rs72780790 | snp | C/T | 0.161267 | 0.233723 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642238 | CATAATATTCTCATG[C/T]ATTTCCTTTCAGATT | 8027 |
rs72780791 | snp | G/T | 0.129664 | 0.219133 | intron-variant | STAM | GRCh38.p7 | 10:17647302 | CCTTGCCAAATCCAA[G/T]GGTCACTTTCTAGTC | 8027 |
rs72780792 | snp | A/G | 0.130008 | 0.219321 | intron-variant | STAM | GRCh38.p7 | 10:17647462 | AACTTCTAAAAGTTG[A/G]GTGCCCTGCGGCTCA | 8027 |
rs72780794 | snp | A/G | 0.129664 | 0.219133 | intron-variant | STAM | GRCh38.p7 | 10:17660154 | GCTAATGAAAATAGT[A/G]TTTCTTATTTTAGTC | 8027 |
rs72780796 | snp | A/G | 0.240765 | 0.249829 | intron-variant | STAM | GRCh38.p7 | 10:17664167 | ACAGAATTGGGTTAC[A/G]TATTCACAGATCAAC | 8027 |
rs72780799 | snp | C/T | 0.130351 | 0.219509 | intron-variant | STAM | GRCh38.p7 | 10:17667965 | AAAAATAGAAGATGA[C/T]GGTTGGAAGGTAGGA | 8027 |
rs72780800 | snp | A/C | 0.131038 | 0.219882 | intron-variant | STAM | GRCh38.p7 | 10:17668906 | TGGTGATTTTTAATA[A/C]AGCTGCTATAAACAT | 8027 |
rs72782503 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17675579 | GTTTATATAAAGTTT[A/G]GACAACTATGTTTAT | 8027 |
rs72782505 | snp | A/G | 0.12932 | 0.218944 | intron-variant | STAM | GRCh38.p7 | 10:17677243 | GAATAGTTTCATTTC[A/G]ACACCCCTTTCCCCA | 8027 |
rs72782510 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | STAM | GRCh38.p7 | 10:17680210 | ATTCTTTAGATTGTA[A/G]CAAAATAAACATAGC | 8027 |
rs72782512 | snp | C/T | 0.126909 | 0.217598 | intron-variant | STAM | GRCh38.p7 | 10:17683239 | TGCCATCACAGCTCA[C/T]TGCATCCTCGACCTC | 8027 |
rs72782513 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685457 | CAAACTGTTCCAGAT[A/G]GGGCCAGATGAGAGT | 8027 |
rs72782514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689967 | CAGTCCACAAAGGGA[C/T]TTACTCTTGTAAGAA | 8027 |
rs72782571 | snp | A/G | 0.0125291 | 0.0781508 | intron-variant | STAM | GRCh38.p7 | 10:17695245 | TCTTGATGACAGGTA[A/G]TGTTAATATTACATT | 8027 |
rs72782572 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696314 | GAGTGTACTCTTTGC[A/G/T]AATGTTTTGCACTGT | 8027 |
rs72782577 | snp | G/T | 0 | 0 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715390 | TGTGAGCTAAAGAGA[G/T]ATATATATATATGTG | 8027 |
rs73603843 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | STAM | GRCh38.p7 | 10:17647822 | CTTTAAATACCTAGC[A/G]TATTCTGGTGACTCC | 8027 |
rs73603845 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | STAM | GRCh38.p7 | 10:17648842 | ATCCTACTTAAAGGG[A/G]AATGCAAGTTTTTTT | 8027 |
rs73603851 | snp | A/G | 0.146985 | 0.227789 | intron-variant | STAM | GRCh38.p7 | 10:17652450 | TCATGAGTTTTCAAC[A/G]TAATATCTGCTGATA | 8027 |
rs73603855 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | STAM | GRCh38.p7 | 10:17655707 | AAGAATTTCATTATC[A/C]CTTGGTCAAGACCAA | 8027 |
rs73603860 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17659948 | TCTTAGGATAAACAA[C/T]AGGCAGTTATTTTCT | 8027 |
rs73603867 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17669216 | TGATTTGAAATATTT[C/T]TTTTATATATTATAT | 8027 |
rs73603869 | snp | G/T | 0.145642 | 0.227177 | intron-variant | STAM | GRCh38.p7 | 10:17672818 | GAATGTTGTTCTTCT[G/T]TGACATCTTACAGCA | 8027 |
rs73603872 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | STAM | GRCh38.p7 | 10:17679043 | ACATTTGGCTGTTGT[G/T]AATACTATTAATACT | 8027 |
rs73603876 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | STAM | GRCh38.p7 | 10:17680163 | TTCTTAAGGTATAAT[A/C]TTAGGTTATTGATTT | 8027 |
rs73603884 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | STAM | GRCh38.p7 | 10:17700925 | ATATATTGAATATCA[C/T]TGGAGATGATTCATG | 8027 |
rs73603889 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | STAM | GRCh38.p7 | 10:17704074 | TCGCTTAAGAGAATC[C/T]CTGTTAGCAGTTGGT | 8027 |
rs73603891 | snp | A/G | 0.148661 | 0.22854 | intron-variant | STAM | GRCh38.p7 | 10:17707079 | GGACCCCCTTTTCAC[A/G]AACTCATCACGGTGA | 8027 |
rs73603892 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | STAM | GRCh38.p7 | 10:17708261 | TAGTTGTGTCAGAGA[C/G]TACATGGTCCACAAA | 8027 |
rs73603893 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | STAM | GRCh38.p7 | 10:17710145 | ATTTTAGTATTAGCC[A/G]GAACTGCCACTTTTC | 8027 |
rs73603894 | snp | C/T | 0.031825 | 0.122064 | intron-variant | STAM | GRCh38.p7 | 10:17711271 | AGGTGTCACTGATGA[C/T]GGTTTTCTAAAGCTA | 8027 |
rs74118005 | snp | G/T | 0.186421 | 0.24178 | intron-variant | STAM | GRCh38.p7 | 10:17682925 | CTATTTTTGTGTTCA[G/T]GCACATTTAGAATTA | 8027 |
rs74118008 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | STAM | GRCh38.p7 | 10:17686929 | CATAGAGGAGTTATT[C/T]CTTCTCTGGTATCTG | 8027 |
rs74118010 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688259 | TTTTCTTCATTCCCA[A/G]GTAATTTTTACTACT | 8027 |
rs74118013 | snp | A/T | 0.185155 | 0.241444 | intron-variant | STAM | GRCh38.p7 | 10:17694248 | AAATTTTAAGTTTTG[A/T]GAAGGCCAGAGTTGT | 8027 |
rs74118014 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697645 | GTTTACTATATTTCT[A/C]CATAATATTGTGCTT | 8027 |
rs74118015 | snp | C/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698494 | CTCATGTTTTTCACT[C/G]TGGACGATCTAAAAG | 8027 |
rs74118016 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17700725 | AAACAAGTTTTTACA[C/G]TCGTATTCATATCAT | 8027 |
rs74118021 | snp | C/T | 0.115088 | 0.210473 | intron-variant | STAM | GRCh38.p7 | 10:17712810 | TTTTTCTTTCTTTTT[C/T]TAATGGGAGCAGTGC | 8027 |
rs74118022 | snp | G/T | 0.115088 | 0.210473 | intron-variant | STAM | GRCh38.p7 | 10:17712908 | CGTGAGGGGTGCAGC[G/T]GCAGAGAGTTGATCA | 8027 |
rs74118023 | snp | C/T | 0.115088 | 0.210473 | intron-variant | STAM | GRCh38.p7 | 10:17713189 | ACTTCTTCTCAGCCT[C/T]ATTTGCCTCTTGCCT | 8027 |
rs74118024 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714059 | TTCTGTTTACCTGAA[A/G]TGTACTTTCCTAGGG | 8027 |
rs74120045 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | STAM | GRCh38.p7 | 10:17651581 | AAGCTGTTTTTTCTA[A/G]TGCCTTTAGGTTATC | 8027 |
rs74120046 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | STAM | GRCh38.p7 | 10:17652286 | ATAACTGAGAAGAAT[C/T]GTGCCACTGATTTTG | 8027 |
rs74120047 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | STAM | GRCh38.p7 | 10:17652957 | ACTAGTCTTTGTTTC[C/G]TAGGAGACAGCCTCT | 8027 |
rs74120049 | snp | A/G | 0.029116 | 0.117091 | intron-variant | STAM | GRCh38.p7 | 10:17654702 | ATTACCAAAACTTGA[A/G]CAATGATAGGTAAAT | 8027 |
rs74228782 | snp | A/G | 0.131381 | 0.220067 | intron-variant | STAM | GRCh38.p7 | 10:17669051 | TGTCCCCACAGTCTC[A/G]GTATGGTTTTGTTTT | 8027 |
rs74456124 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | STAM | GRCh38.p7 | 10:17650505 | TTACTTAGTCATACA[A/G]GTCGTGAACTTGGGA | 8027 |
rs74488146 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | STAM | GRCh38.p7 | 10:17704088 | CTCTGTTAGCAGTTG[A/G]TTGGTTGGTTTATTT | 8027 |
rs74490561 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | STAM | GRCh38.p7 | 10:17678985 | AGGCTGAATACTATT[C/G]CATTGTATATCACAT | 8027 |
rs74538188 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17709776 | CTGCCCTCTCTTGCA[C/T]TACTCATCCTCAAAG | 8027 |
rs74785158 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | STAM | GRCh38.p7 | 10:17655534 | TGATATATAGCAGGT[A/G]TTATACACCTGTAAA | 8027 |
rs74790963 | snp | G/T | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17654758 | CTTCCAAACTGCTTT[G/T]ACATATTGGTGATAG | 8027 |
rs74966187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17654725 | AGGTAAATTTGAGCT[A/G]GTTCTCCTCTTTTCC | 8027 |
rs74990719 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | STAM | GRCh38.p7 | 10:17653587 | CATGGATTCAAACAA[A/C]AGTGGATCAAAACTT | 8027 |
rs75036766 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17658659 | TCAGCTAATTTTTGT[A/G]TTTTTTTTGTAGAGG | 8027 |
rs75075930 | snp | A/C | 0.0539704 | 0.155153 | intron-variant | STAM | GRCh38.p7 | 10:17677263 | CCCTTTCCCCACCAT[A/C]CTTTCCAAAAGTCAC | 8027 |
rs75228706 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17685242 | TACTGTTTTTGTAGG[C/T]ACAAGGTATTTTCCT | 8027 |
rs75260471 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17698923 | CTGCAGCAGATGTTT[C/G]TTTTCCTTTATAGGA | 8027 |
rs75439107 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | STAM | GRCh38.p7 | 10:17653524 | TGTTTGGAACCCTCC[C/T]AGATCTAGCTCCATA | 8027 |
rs75499514 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | STAM | GRCh38.p7 | 10:17704752 | TGGTAAAATGAAAAA[C/T]GGCACTTTAAGATTT | 8027 |
rs75570135 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644874 | GGGAGCTCTGGTTAA[-/AA]GGGTAGACTCTCAAA | 8027 |
rs75578503 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17669714 | TCTTTTTTTTTTTTT[C/T]TGAGATGGAGTCTCG | 8027 |
rs75723163 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | STAM | GRCh38.p7 | 10:17670171 | GTTGTTGACTAGGCA[A/G]TAGGGAATGGGATCC | 8027 |
rs75921400 | snp | A/G | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17665154 | GGAAACATGGCTCTC[A/G]GTGGTGTTGTGAAAA | 8027 |
rs75977793 | snp | A/G | 0.0391387 | 0.134304 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715197 | GTTAAATTAATTTAC[A/G]TTGCTATTTTATTTT | 8027 |
rs76028594 | snp | C/G | 0.00953873 | 0.0683987 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716612 | TCTTTTGATAAATTC[C/G]TGTTTACCAATGTTA | 8027 |
rs76045842 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17674097 | TTTGTAAGCCTGACC[C/T]GATTTAGTCTTTATA | 8027 |
rs76048099 | snp | A/T | | | missense | STAM | GRCh38.p7 | 10:17700261 | AGAACCAGAGCCGGA[A/T]CCAGCCTTTATTGAT | 8027 |
rs76090276 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17648663 | ACCATTCTTACCTTA[C/T]TTCAGTCATTGTTAT | 8027 |
rs76101190 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | STAM | GRCh38.p7 | 10:17683504 | ATATTTGTAGTGGTG[A/G]CTCTGTGTTAAATTT | 8027 |
rs76148048 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17683236 | TGGTGCCATCACAGC[G/T]CACTGCATCCTCGAC | 8027 |
rs76216720 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | STAM | GRCh38.p7 | 10:17672288 | CATTGTTGAAAACTT[A/G]CTGTGGGCCATTCAA | 8027 |
rs76219291 | snp | A/G | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695799 | TGTTTTTTAAAAATC[A/G]GTTCAAATTGATTTA | 8027 |
rs76221699 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697724 | ATAATCTCCCCTCTA[-/TTTA]GGAAAACAGAAAAAT | 8027 |
rs76360420 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672855 | TTTGTGTTATGGTCA[A/T]TTATCAAATGATAAG | 8027 |
rs76381388 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669903 | TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAC | 8027 |
rs76404046 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | STAM | GRCh38.p7 | 10:17712483 | GTAGCATTAAATTAC[C/T]GTCTCTTATAATAAA | 8027 |
rs76422696 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | STAM | GRCh38.p7 | 10:17699186 | CTTTCTCTTTTACAA[A/G]AGTTTTTAATCTTTC | 8027 |
rs76429783 | snp | A/C | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17677764 | TTGTTTCTCCCTTCA[A/C]CATGCTCTTTAGGTG | 8027 |
rs76481764 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17686351 | TTTACAGTGAACATA[C/T]TGGTTTTGTACTTAA | 8027 |
rs76511688 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | STAM | GRCh38.p7 | 10:17681225 | TTTTTTAATGTAGGT[G/T]CTTATAGGTATAAAT | 8027 |
rs76542226 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | STAM | GRCh38.p7 | 10:17694555 | ACACGTTTGAGATCT[A/G]TTTTGGAGGATTTGT | 8027 |
rs76592203 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17649944 | TAGTGTTGTAGTTAT[C/G]TTGACTTGAAACCCA | 8027 |
rs76603297 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17647854 | GGATTTATGTTCTTA[C/T]TCTCAGCCTCTTGCC | 8027 |
rs76604181 | snp | A/G | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672850 | TGTGATTTGTGTTAT[A/G]GTCATTTATCAAATG | 8027 |
rs76616446 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680877 | ATGCGTCTGTGGACA[C/T]TTGGGTTGCTTCTGC | 8027 |
rs76634322 | snp | A/C | 0.0170474 | 0.0909192 | intron-variant | STAM | GRCh38.p7 | 10:17678049 | TTTAATATGTTCATA[A/C]GTTTGTGCAACAGTA | 8027 |
rs76693317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17685865 | TTCAATTTTCAATTA[A/G]TAATATGTGAGTTTC | 8027 |
rs76756752 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17657861 | TCTCTTTTTTTTTTT[C/T]CCTTAGTTTAGCTTG | 8027 |
rs76766346 | snp | C/T | 0.00308201 | 0.0391345 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714830 | AAATGCCACTGACAA[C/T]GTTATGAGATTCATT | 8027 |
rs76859238 | snp | C/G | 0.0829062 | 0.185956 | intron-variant | STAM | GRCh38.p7 | 10:17652551 | CAATTTATATTTGAT[C/G]AGATAAACTGTTAAC | 8027 |
rs77053766 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17705924 | AAAAAAAAAAAAAAT[A/T]AGCCAGGCTGGGGCA | 8027 |
rs77062281 | snp | C/T | 0.124837 | 0.216412 | intron-variant | STAM | GRCh38.p7 | 10:17669848 | GACTACAGGCACCCG[C/T]CCCTATGCCCTATGC | 8027 |
rs77062577 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | STAM | GRCh38.p7 | 10:17698989 | TTGAATGGAATGATT[A/G]TATTTCTTAGGTTGG | 8027 |
rs77089013 | snp | G/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17667141 | TAATTTTTTTTTTTT[G/T]TTGAGACAGAGTTTC | 8027 |
rs77095842 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17660058 | ATTATCAAAAAAAAA[-/A]ATCCACAAAACTAGC | 8027 |
rs77105264 | snp | A/C | | | missense | STAM | GRCh38.p7 | 10:17705601 | AGAAAACATTCAGAA[A/C]TCTCAGAACTTAATG | 8027 |
rs77158233 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17700414 | AGTCTGCATCGTCTA[A/G]ATTGCTTGAATTTTT | 8027 |
rs77204065 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17712705 | TTCACATAGCTAACC[C/T]AGTGTCTTACAGTGG | 8027 |
rs77210930 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672864 | TGGTCATTTATCAAA[A/T]GATAAGTAGGTATTT | 8027 |
rs77300815 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17652996 | GGAATTTTCTGAGTG[A/T]TAAGAGCATCTTTGT | 8027 |
rs77400741 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | STAM | GRCh38.p7 | 10:17684538 | TACAGTTTTTCAACC[A/G]TGTTATTAATAAAAA | 8027 |
rs77411641 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643628 | ACTCCCGGGAAGGAG[C/T]CAGCGTTACCTCAGC | 8027 |
rs77437843 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | STAM | GRCh38.p7 | 10:17664684 | AGAGGACATGAGTTT[C/T]CCAAAGACAAATTCA | 8027 |
rs77536950 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | STAM | GRCh38.p7 | 10:17661488 | TGTCTTTATGTAGAT[A/G]GCATCTGTATTTGCA | 8027 |
rs77537869 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17653185 | CCACTGTGTGGTCCT[A/G]TTTCATAAATCATAC | 8027 |
rs77549987 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17687350 | CATGGTGGTGCGCGC[C/T]TGTAATCCTACTCGG | 8027 |
rs77708060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17669145 | ACTTTATTCTTTTCT[A/G]TTTGGCTACCAAATA | 8027 |
rs77741328 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | STAM | GRCh38.p7 | 10:17699047 | AAGCACACAACACGG[A/C]GTACCCAAGTGATTG | 8027 |
rs77807508 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17684155 | TTCACCTGTGCATGC[A/G]TGGGTTTTTCAGAAG | 8027 |
rs77808232 | in-del | -/T | 0.313082 | 0.241911 | intron-variant | STAM | GRCh38.p7 | 10:17677965 | GATAAAAGTTTTTAC[-/T]TTTTATAAATACATA | 8027 |
rs77825304 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643798 | AATTTCCATTTCCTT[C/T]CAGAGGGAATACAAG | 8027 |
rs77845592 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | STAM | GRCh38.p7 | 10:17679574 | TTGATGTTTAATTTG[C/T]GTGTGTTTTTTTTTT | 8027 |
rs77935610 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | STAM | GRCh38.p7 | 10:17705122 | TTTAAAAAAAAAATA[C/T]TGTGGAGGAACCAAC | 8027 |
rs77981128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17667706 | AGTAACCAGAGTGCT[A/G]TAATGGAAAATAAAA | 8027 |
rs78161203 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17647105 | GGGATTTTTGTTTGA[C/T]TTTTTCACTGCCGTA | 8027 |
rs78192901 | snp | C/T | 0.0901694 | 0.192235 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698412 | ATGTAGATCCTGGAG[C/T]CATTTCATCTTTTTT | 8027 |
rs78360496 | snp | C/T | 0.113685 | 0.209567 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713932 | CCACCGCAGTCCTGC[C/T]GGTGATCTTAGCTGC | 8027 |
rs78405687 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | STAM | GRCh38.p7 | 10:17647612 | GCTGCTTACCGGTAG[C/T]GTGATTTTTGGCCTA | 8027 |
rs78414059 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698463 | ATGCAGCTTCAATAT[A/G]AGTTTTCTAGTTTTT | 8027 |
rs78664097 | snp | G/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697972 | ATCTTTTTATTTCCA[G/T]CAGCTCCTAATAGTG | 8027 |
rs78665201 | snp | C/G | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672845 | AGCAGTGTGATTTGT[C/G]TTATGGTCATTTATC | 8027 |
rs78698536 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17709731 | GAAACCTTTCCAGCA[C/G]TGTTAGGATTGCCCA | 8027 |
rs78704099 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17666863 | AGACCTCTTTCAAGT[C/T]TTTTTTTCTTCCTAT | 8027 |
rs78710549 | snp | A/G | 0.093417 | 0.194889 | intron-variant | STAM | GRCh38.p7 | 10:17681090 | TACATTCCCACCAAC[A/G]GTGCACAAGTGTTTC | 8027 |
rs78776567 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | STAM | GRCh38.p7 | 10:17712526 | AATGAATTTGTGCCA[A/C]GTACAAGAGCACTGA | 8027 |
rs78784497 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643221 | CAATATTAGTTTCCA[C/T]GCTACATTTGGAGAT | 8027 |
rs78789039 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688888 | GGATATCCTTAAAAG[A/T]TAGGGATGACTTGAG | 8027 |
rs78886399 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17657863 | TCTTTTTTTTTTTTC[C/T]TTAGTTTAGCTTGGC | 8027 |
rs78887360 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672846 | GCAGTGTGATTTGTG[A/T]TATGGTCATTTATCA | 8027 |
rs78988313 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17671578 | TCAGGTGTCCCATGA[C/T]AGGCGGGTTACTACT | 8027 |
rs79056392 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17691963 | GTGTATTACCTCTAC[A/C]TACGTTATAAGCCCC | 8027 |
rs79073084 | snp | G/T | 0.0126979 | 0.078662 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715491 | ACAGTAGCTAAATTT[G/T]TGGTGCAATTATAGC | 8027 |
rs79081430 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689220 | CTTAAAATATGTGCT[C/G]ATTTACTACACTGTC | 8027 |
rs79129885 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17652865 | CTCAATCAGAGCACT[C/T]CCACTTGGGTTTGCT | 8027 |
rs79209408 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678269 | GTGTAATTTTTTTTT[-/T]TGGAAGACAGAGTCT | 8027 |
rs79254368 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | STAM | GRCh38.p7 | 10:17663195 | ATTTGTTTTTCTTAA[C/T]GTTAACGTTATTCTC | 8027 |
rs79344034 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | STAM | GRCh38.p7 | 10:17695362 | CCCAGATGCTGCTCT[A/G]TATGACAGTTGGCTG | 8027 |
rs79525490 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17661912 | GGTCCCATCCATCCC[C/T]TTGTTGTATTTACAT | 8027 |
rs79551044 | snp | G/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672841 | TTACAGCAGTGTGAT[G/T]TGTGTTATGGTCATT | 8027 |
rs79678367 | snp | A/C/G | 0.000510955 | 0.0159762 | intron-variant, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714534 | TTGAGTGTTTTTCTT[A/C/G]CTCCACAGTACAATG | 8027 |
rs79686898 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672862 | TATGGTCATTTATCA[A/T]ATGATAAGTAGGTAT | 8027 |
rs79710144 | snp | A/T | 0.0652144 | 0.168387 | intron-variant | STAM | GRCh38.p7 | 10:17681146 | TTACCATTTTTTCTG[A/T]TTTTCTTTATAGTAG | 8027 |
rs79732928 | snp | A/G | 0.172351 | 0.237636 | intron-variant | STAM | GRCh38.p7 | 10:17656245 | GTTGCAGTGAGCCGA[A/G]ATCGCACCACTGCAC | 8027 |
rs79796581 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | STAM | GRCh38.p7 | 10:17650453 | ATTTTTCTTCTCAAT[G/T]ATGCTTTTTGTCTGT | 8027 |
rs79797179 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17666864 | GACCTCTTTCAAGTC[C/T]TTTTTTCTTCCTATA | 8027 |
rs79825475 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17672848 | AGTGTGATTTGTGTT[A/T]TGGTCATTTATCAAA | 8027 |
rs79888402 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17678219 | TAAATGGAGCTCTGC[A/G]ATACATGTTCTTTTG | 8027 |
rs79952113 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17680420 | TTTTGACTACTCTTT[C/T]TTTTTTTTTTTCTTT | 8027 |
rs80008307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672860 | GTTATGGTCATTTAT[C/G]AAATGATAAGTAGGT | 8027 |
rs80013236 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | STAM | GRCh38.p7 | 10:17647821 | GCTTTAAATACCTAG[A/C]GTATTCTGGTGACTC | 8027 |
rs80039428 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642697 | AAATGGAATTGCTGG[A/G]TCCTAAGGTTTTAAA | 8027 |
rs80103473 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17687119 | TTAATACGGAAGAAT[A/C]ATGCCCTGCACACCT | 8027 |
rs80183407 | snp | C/G/T | 0.0150737 | 0.0856109 | intron-variant | STAM | GRCh38.p7 | 10:17683389 | CTGGTCCCAAACTTC[C/G/T]GGACTCAAGCCATCT | 8027 |
rs80211903 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | STAM | GRCh38.p7 | 10:17693677 | AACTGTTCTATAATA[C/T]CCAGTGTACTAATGA | 8027 |
rs80316791 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17673398 | AAAGCAGTATTTTTC[A/G]TGTTTTGCTCAGTGA | 8027 |
rs80345372 | snp | G/T | 0.5 | 0 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696178 | CATTTTTTTTTTTTT[G/T]AGTGGAAGAAAATAA | 8027 |
rs111301056 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | STAM | GRCh38.p7 | 10:17646607 | CAGTGTAGCAACATT[A/G]TTTTGCTCCAGAAAA | 8027 |
rs111379948 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | STAM | GRCh38.p7 | 10:17700570 | GTTGTTTACAGTTTT[G/T]ACAGTGTAGTAGTGA | 8027 |
rs111429855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706630 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 8027 |
rs111456620 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17660226 | TATAAAGAAAAATCA[A/G]TGCCTTTTATTTTAT | 8027 |
rs111458096 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17690878 | ATAAGACAAGTGTTA[C/T]TGTTACATTTAGAAC | 8027 |
rs111510976 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715341 | TATGTTGTCGTGTGT[G/T]TCAGTTTCACATTAA | 8027 |
rs111515189 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17712183 | GCTTTACACAAAGTA[A/G]CTTATTCCTCATAAT | 8027 |
rs111632550 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17658536 | ATTTCTTCTTTTTTT[A/G]GTCTTGCTCTGTCGC | 8027 |
rs111634197 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696701 | AATAGTGTAAGTTGA[A/G]TACTACAAAAGATAA | 8027 |
rs111635990 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | STAM | GRCh38.p7 | 10:17692363 | TGACTGATGTGTTCA[A/G]ACTCAAAAGGGAAAA | 8027 |
rs111641650 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17693479 | AATTACTGTCACATG[G/T]ATCCTTTCAGTCTAT | 8027 |
rs111716968 | snp | A/C | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17693030 | CTCCTCTAAGTGTCT[A/C]GTTGCTCTCTGTGTT | 8027 |
rs111786483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695881 | GCCGTAACAAACTAC[C/T]GTAGACTAACTGGTT | 8027 |
rs111794508 | snp | A/G | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17666210 | AGATATAGTTGACTA[A/G]AGGTGGAAAACATCA | 8027 |
rs111808166 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | STAM | GRCh38.p7 | 10:17660032 | TTTTCTTTCCTTCAG[G/T]CCCCTCTCCATATTA | 8027 |
rs111809697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670246 | TTACTTTTTTATTTT[A/G]CTAAGTCTTAAAAAC | 8027 |
rs111847376 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17682234 | TCATAAAATGAAATA[C/G]TATTGTCAGTACTCC | 8027 |
rs111883150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707139 | TACTGGCCGGGTGCG[A/G]TGGCTCATACCTGTA | 8027 |
rs111949596 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716157 | GCACTATTTAAACAA[C/T]GGAAAAGTTGAGTCG | 8027 |
rs112006084 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17695962 | GGCCCACTTTCTGGT[A/T]TGTAGAAGGCTGTCA | 8027 |
rs112031205 | snp | A/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17646381 | GAAGGACAAAATACC[A/T]CCCAGTTGAGAACCG | 8027 |
rs112178818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17683390 | TGGTCCCAAACTTCC[A/G]GACTCAAGCCATCTG | 8027 |
rs112364914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659350 | GGTAATGAATACATT[A/G]TTGCTGTTATTATTT | 8027 |
rs112415800 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | STAM | GRCh38.p7 | 10:17706722 | TAATTATTTACTTAA[G/T]AACCTTAGTTCTTCA | 8027 |
rs112457951 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647102 | ACAGGGATTTTTGTT[C/T]GATTTTTTCACTGCC | 8027 |
rs112495785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17660203 | GGTAGACCTATATAT[A/G]ATTTTTTTATAAAGA | 8027 |
rs112528084 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696986 | GTGCAGTGGTGCGAG[C/G]TCGGATCATTGCAAC | 8027 |
rs112578531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17693625 | GCTTTTCTCATGCAA[C/T]ATTATGTTTGAGATC | 8027 |
rs112629253 | in-del | -/ATTAATAT | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17649789 | TAAATCTTTTTTTAC[-/ATTAATAT]ATTAATATAGATGGG | 8027 |
rs112656564 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17700047 | TTACTGCCAAAATCT[G/T]CAACTCAGTTATTTC | 8027 |
rs112786527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685829 | AACTGTAGAATTCTA[A/G]TCACACAGTTCAAGA | 8027 |
rs112858458 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | STAM | GRCh38.p7 | 10:17702748 | GGCGCAGTGGCTCTC[A/G]CCTGTAATCCCAGCA | 8027 |
rs112898248 | snp | C/G | 0.5 | 0 | missense | STAM | GRCh38.p7 | 10:17705616 | CTCTCAGAACTTAAT[C/G]TGAAAGTGATGGAGG | 8027 |
rs112940364 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17664840 | TTTGTAAAGTGCGGC[A/G/T]ATCTTTTTAAGAGGA | 8027 |
rs112946907 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17670817 | AGCTTAACATTAAGG[G/T]AATAATTTGATATTT | 8027 |
rs113007436 | snp | C/T | 0.130351 | 0.219509 | intron-variant | STAM | GRCh38.p7 | 10:17678496 | TGATCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 8027 |
rs113147728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697412 | GTTTCTCTAGTGTGT[A/G]GTCCCAGACTTGAAA | 8027 |
rs113300139 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17681071 | CACAGCACCTGTAGC[A/G]TTTTACATTCCCACC | 8027 |
rs113442204 | snp | A/G | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17668548 | ATTGTGTAATGCCAC[A/G]TATCTGTCATTACAG | 8027 |
rs113489494 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17691539 | AAATAAATAAATGCC[C/T]GTGCATTTGTTTGAC | 8027 |
rs113549693 | snp | A/G | 0.00115578 | 0.0240116 | intron-variant | STAM | GRCh38.p7 | 10:17684780 | TTTAATCTGTACCAC[A/G]AAATTACCTGCCACA | 8027 |
rs113632266 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | STAM | GRCh38.p7 | 10:17705449 | GCTAAAATGCAGGAT[A/G]TTTTTGTTATAAGTG | 8027 |
rs113681947 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | STAM | GRCh38.p7 | 10:17695295 | TGTATGGCTTCTGTG[C/T]TTCATATTATTCCTG | 8027 |
rs113734476 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17666683 | ATTACAGGCATGAGC[C/T]ACCCTGCCTGGCCTT | 8027 |
rs113774157 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666406 | TTTTTTTTTTTTTTT[C/T]TTTTTTGAGACAGAG | 8027 |
rs113825437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646481 | ACCGAATTATTTAGC[A/G]TTCAAGATAGTTTTA | 8027 |
rs113930230 | snp | C/T | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17687362 | CGCCTGTAATCCTAC[C/T]CGGGAGGTTGACACA | 8027 |
rs113939469 | snp | C/G | 0.5 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17659623 | ACAGGTGCATGCCAC[C/G]AGGCCCAGCTAATTA | 8027 |
rs113966408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691115 | CAGAAGTGTCTGATA[A/G]TTAAAACATTATCTA | 8027 |
rs114024290 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17692547 | GCTAAATTCTGATTT[A/G]CCTTGAATGCTATGC | 8027 |
rs114024713 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17654513 | AGGCGTGGGTCACCG[C/T]GCCCGGCTAAACCAG | 8027 |
rs114063930 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17647167 | GAAGAACTTTCAGTA[A/G]ACATTTATGGAATAA | 8027 |
rs114132617 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | STAM | GRCh38.p7 | 10:17711785 | AGACACTGCCAAGGT[C/G]GAAGAATGCTTGTTC | 8027 |
rs114139528 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17706064 | CAGCGACACCCTGTC[G/T]CTAAAATAAATAAAT | 8027 |
rs114164157 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689643 | ATACATTCCTTGACA[A/G]CAGAAACAATGTTTA | 8027 |
rs114171087 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | STAM | GRCh38.p7 | 10:17681737 | AGCATGTTTAAGTGA[C/G]AGGTATGAATCTTGT | 8027 |
rs114302876 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17655516 | AACTAGCAGGTGATG[A/C]TGTGATATATAGCAG | 8027 |
rs114323034 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17661742 | TTCATAATCTCTCAA[A/G]ATGTTGACGTTTTAA | 8027 |
rs114325814 | snp | C/G | 0.0185938 | 0.0946107 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643737 | CGAGCAAGTTTGTCA[C/G]CTCACGCAGCTAATT | 8027 |
rs114343618 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17649090 | TCTGAGACGCTTTAC[C/G]TAATAATCTTCTGTA | 8027 |
rs114390815 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | STAM | GRCh38.p7 | 10:17708264 | TTGTGTCAGAGACTA[C/T]ATGGTCCACAAAACT | 8027 |
rs114488014 | snp | A/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687731 | AAAAGCAGACACTTT[A/T]CCTTGTCTTACTGAT | 8027 |
rs114491512 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17691828 | TTTCATTTTTAAATT[A/G]TTTGCCCTGGGAATG | 8027 |
rs114524370 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17676144 | AAGAAAGCACAGTAG[C/T]ACAGTTTGGATATTT | 8027 |
rs114529501 | snp | C/T | 0.000922281 | 0.0214544 | missense | STAM | GRCh38.p7 | 10:17708858 | AGAGCTACAGTCTTC[C/T]CCCGGAGCAGCTGTC | 8027 |
rs114532466 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17677849 | TCCTAATTTTTCTAT[A/G]TAATTATTAAAAAGG | 8027 |
rs114536187 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17710318 | AGTGAAGTTCTGTAG[C/T]GCTGTGGTACCCTGC | 8027 |
rs114650581 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | STAM | GRCh38.p7 | 10:17654517 | GTGGGTCACCGCGCC[C/T]GGCTAAACCAGGTAT | 8027 |
rs114719238 | snp | G/T | 0.0115144 | 0.0749975 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716489 | TCAAATTTCACATTT[G/T]AAATACTATAAGTTA | 8027 |
rs114719577 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17668061 | GTCCATCGGAGTTAA[G/T]AAGATGTGATAGAAG | 8027 |
rs114722365 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | STAM | GRCh38.p7 | 10:17677135 | CCTTTTAATGGTTCA[G/T]TAGCCAATTTTATTT | 8027 |
rs114925947 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | STAM | GRCh38.p7 | 10:17652098 | TAAAATGAGATCATT[A/G]TGAAGCTTTGAATTC | 8027 |
rs114991925 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | STAM | GRCh38.p7 | 10:17680768 | CATTTGTCCTGTTGT[C/G]ACCAGCTTATTTCAC | 8027 |
rs115069594 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17646376 | CCCTGGAAGGACAAA[A/C]TACCTCCCAGTTGAG | 8027 |
rs115111106 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17673649 | CCCTCATGATGGGGA[A/G]ATAAGTAGTTAAGGA | 8027 |
rs115122209 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17711857 | TTTAAATGGCAGTAG[C/T]GTAGATGGATTCATA | 8027 |
rs115176677 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17692403 | AGCAAAGGAGCCATA[A/G]GGGGAGAACGTTGTA | 8027 |
rs115217338 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17669340 | TTTGACATTTGGTAG[G/T]ATATGGTCTTGAGGT | 8027 |
rs115223885 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17674405 | GTAGTCACATAGTGC[C/T]TGGGACTAGGGTCAT | 8027 |
rs115323131 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17686374 | GTACTTAATAACATC[C/T]CGCCTTTTTTTTTTT | 8027 |
rs115331474 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17704754 | GTAAAATGAAAAATG[A/G]CACTTTAAGATTTTC | 8027 |
rs115404437 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | STAM | GRCh38.p7 | 10:17662256 | TCAGCTCAACTATCT[A/G]AGTTCCAGTGCTTTT | 8027 |
rs115496861 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17671102 | TTAGTTCATTCAGCA[A/G]AGATTTGAGTTCCCA | 8027 |
rs115500417 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645219 | AATTTGAACGCACGT[A/G]GGAACTACCTTGGCA | 8027 |
rs115513800 | snp | A/C | 0.0115144 | 0.0749975 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716740 | AGTGAATAGAAAAAA[A/C]TACCCTTATTACAAC | 8027 |
rs115701372 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17647423 | ACTTAGCTCCTTTTA[A/C]ATTTTTTTGCTTCCC | 8027 |
rs115702226 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17678581 | ATTCTTCTGAGGTTC[A/G]TTTATGTTGTAGCTT | 8027 |
rs115773985 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689387 | ATGTGCTTTCTTCCC[A/G]AGGCATTTCCAGTTT | 8027 |
rs115809107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17679231 | TCCAATATTTGGTAT[C/T]TTTCCTTTCTTAAAA | 8027 |
rs115992627 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17691513 | ACAGAGCGAGACTCA[A/C]ATAAATAAATAAATA | 8027 |
rs116033307 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17658926 | TGCAGACCATTGACA[A/T]GTAAAGTGACTGTTA | 8027 |
rs116043440 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17683787 | AGTTGACTGAATTTT[C/T]TGCTAGTTGTGTATG | 8027 |
rs116044470 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17655802 | AAAATGGAGACTGCT[A/G]TTGAAGATCTTGGTG | 8027 |
rs116098171 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696379 | AGAAAAAAAAAACCT[G/T]GCTGCTGTGTACCAG | 8027 |
rs116101557 | snp | C/T | 0.00303846 | 0.0388587 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688164 | TACGTTCCCAGCTAT[C/T]GGCTCTCAGGTATTT | 8027 |
rs116169662 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17674294 | ACTCTTAGTAGTAAC[G/T]GTCCTAACACTTAGC | 8027 |
rs116205402 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17678750 | TTTTTCATCATCCCA[C/T]GTAGAAACTCTACAC | 8027 |
rs116222997 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17691010 | CACCATAAAAGTTCA[A/C]ATCTGTCTAATTGTG | 8027 |
rs116262004 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645149 | ATTTTATTTTTTTCT[C/G]ACTTGAAGATAATAA | 8027 |
rs116289462 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | STAM | GRCh38.p7 | 10:17680541 | CTCTCGAATAGCTGG[G/T]ACTACAAGTGTGTGC | 8027 |
rs116343068 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | STAM | GRCh38.p7 | 10:17673463 | ATTCTAGGCCCCATT[C/T]GCAATGACAGTGTTT | 8027 |
rs116451608 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17690476 | TACATATAAAGTAAA[A/G]TATGATGAGGTAGAA | 8027 |
rs116626483 | snp | A/C | 0.0655868 | 0.168795 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689566 | TGGTTTTTACTACTC[A/C]GTATAGTTTCTAGAA | 8027 |
rs116638061 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | STAM | GRCh38.p7 | 10:17669783 | GCTCACCGCAAATGC[C/T]GCCTCCCAGGTTCAC | 8027 |
rs116654943 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | STAM | GRCh38.p7 | 10:17702454 | TTTAAATTCCTTTGG[C/T]TATATTTAAAGGAAT | 8027 |
rs116709625 | snp | A/G | 0.00115571 | 0.0240108 | synonymous-codon | STAM | GRCh38.p7 | 10:17695209 | TGAACTTACTTTTAA[A/G]GCTGGAGAAATTATT | 8027 |
rs116724392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17651625 | GTTCCTCTCTGAAAT[A/G]CTTCCATGCTGTTCT | 8027 |
rs116743081 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17680053 | ATTGGCTTTTCTTGA[C/T]TGTGTTTCTGTTGTC | 8027 |
rs116763727 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17684048 | ATTTTCAATAGATGC[C/T]TCACTGTGGCCTCAT | 8027 |
rs116772712 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | STAM | GRCh38.p7 | 10:17656563 | TTTCTTGGAGGGTAA[C/T]GGTACAAATGTTGAA | 8027 |
rs116827403 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17709682 | CATTCTAGCTGGCAA[C/T]AGAAGTTTCTAGGTA | 8027 |
rs116844444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649270 | TTAGCTGGCATGGTG[A/G]TATGCCTGTAGTCCC | 8027 |
rs116979560 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | STAM | GRCh38.p7 | 10:17664799 | AGAAAAAAAATTATT[A/G]TTGCTATTTGGTGTT | 8027 |
rs117486044 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17679379 | CTTGGAGAAATGTCT[A/T]TTCAAGTCCTTTGCC | 8027 |
rs117531399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17667103 | ATAACTTAAAATAGC[A/G]GAAGTGTTCCAGCAG | 8027 |
rs117532963 | snp | G/T | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697660 | ACATAATATTGTGCT[G/T]TAATGAATCTTCATA | 8027 |
rs117540857 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688485 | TGTTTGTTTTTGAGA[C/T]GGAGTCTTTGTTTGT | 8027 |
rs117586884 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | STAM | GRCh38.p7 | 10:17709323 | ATAAAATCTAAATTC[C/T]GTTATTTTAAAATAT | 8027 |
rs117619579 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | STAM | GRCh38.p7 | 10:17687327 | TAAAAGTACAAAAAT[C/T]AGCTGGGCATGGTGG | 8027 |
rs117638768 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17676798 | AGGATAATAGCCAGA[A/G]GTATACTCACGTTAA | 8027 |
rs117775167 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | STAM | GRCh38.p7 | 10:17713004 | TCCCTTCCACTAGTC[C/G]TTTGGGACCGTTCTT | 8027 |
rs117979448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665554 | TTATTGACTACTTAT[A/T]GTATCCTGTCAGTCT | 8027 |
rs117980016 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17665512 | TATATATTCTTCTGC[A/G]TTTATTACTTAATTA | 8027 |
rs118041145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17646153 | GAATCCAACTTGTTA[C/T]ACCTGAGTCATTTCC | 8027 |
rs118064475 | snp | A/T | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17668115 | CATCACTTACACTGT[A/T]ATTAAAAGCTCCAAG | 8027 |
rs137970831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662170 | CTACCTTCCATACTG[A/T]GTTCAGTTTAAGCTC | 8027 |
rs138000495 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon | STAM | GRCh38.p7 | 10:17708826 | GGTTGCAGGGAACGC[A/G]CAGATGAGCCACCTC | 8027 |
rs138064293 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | STAM | GRCh38.p7 | 10:17658539 | TCTTCTTTTTTTGGT[C/G]TTGCTCTGTCGCCCA | 8027 |
rs138069062 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17658248 | TCCATGTACTTTGGG[-/A]TTTTCCAGCTATCTT | 8027 |
rs138108178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710528 | TTCCTGCATATTCTT[C/T]AGTTGTTAGCTTAGC | 8027 |
rs138118943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17682452 | AGAGTACTGGGTAGT[A/G]TGCTTTCATTTTCAT | 8027 |
rs138152016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17685487 | TCCAAAAAAAGAGGC[A/G]CTAAATGCCAGGGTG | 8027 |
rs138183832 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17655023 | TTAGAAACAGATTAA[A/T]TCATTATTCTGTCCT | 8027 |
rs138241768 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | STAM | GRCh38.p7 | 10:17706199 | ACTTGGCAGTTACAG[C/G]ATATAATATACTAAT | 8027 |
rs138283454 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670767 | ATATATTTATATTCA[A/C/T]GTTCCATTATCTCAT | 8027 |
rs138358829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679060 | ATACTATTAATACTA[C/T]TCTGAACATGGGTGT | 8027 |
rs138365444 | in-del | -/A/AA | 0.13739 | 0.223202 | intron-variant | STAM | GRCh38.p7 | 10:17660049 | CCTCTCCATATTATC[-/A/AA]AAAAAAAAAATCCAC | 8027 |
rs138439338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17681395 | GTATTTTAATTTTCT[A/G]TATTTCTTTGTTCTT | 8027 |
rs138467770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648188 | GGACTTCCTGGGTCA[A/G]GTGGGGACTTGGAGA | 8027 |
rs138474658 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17698974 | TTTGCTTTTGGTGAC[C/T]TGAATGGAATGATTA | 8027 |
rs138501183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701144 | ATTATTGGGATTTAA[A/G]TTTGAGATTTCTTGA | 8027 |
rs138521140 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643853 | GGAAAAAAGGCGCAC[A/T]GCTCGACCCGAACTC | 8027 |
rs138624263 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688246 | TTTATTTGAATTTTT[G/T]TCTTCATTCCCAGGT | 8027 |
rs138633924 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715040 | AATTGATACAAGGCT[A/G]TTTGTCTCGTAAACC | 8027 |
rs138716488 | snp | C/G/T | 0.0135027 | 0.0812018 | intron-variant | STAM | GRCh38.p7 | 10:17693588 | TTTGTAGATAGTACA[C/G/T]GGGAAATGCCATTTG | 8027 |
rs138749161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17658833 | TTATGTCTAAAATGA[A/G]TTTCTTATAGACAAC | 8027 |
rs138751592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698071 | GATACTTCACTTCTC[C/T]TTCAAGAGAAGGCTT | 8027 |
rs138762241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17685091 | TTGTTGAAGAGACTG[C/T]GGATTCATGTAACTT | 8027 |
rs138806191 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | STAM | GRCh38.p7 | 10:17657890 | TGGCTAGCAGCATAT[C/T]GGTTTTATTGATCTT | 8027 |
rs138843963 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17661968 | TAATTTAATTGAAAA[A/T]TTTTAACTACTGTGT | 8027 |
rs138975801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701821 | GTACATTGCCTCAGA[A/G]TATAAGAATTACCAG | 8027 |
rs139009042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17667449 | TTTTTAAAACGTGAT[C/T]TTGATTTCCATGTTT | 8027 |
rs139029759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670032 | ACTGCGCCCAGCTGG[C/G]AATTTCCCTTCTTAA | 8027 |
rs139089296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685993 | AATGCCTCATGTTTT[G/T]GGGAAAAATGAATAG | 8027 |
rs139109649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653286 | AAACCGAATATTCCG[C/T]GATAAAAACTGGAAA | 8027 |
rs139154898 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17703501 | TATAGTAGCATAACC[A/T]TGTAAAAACCATGCA | 8027 |
rs139189758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714294 | CTCCATGGTGGTATA[A/G]ACTTATTTCCGCAAA | 8027 |
rs139199006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17712154 | TTTAGTATGTTCCAA[A/G]CACTGTGCTGTATGC | 8027 |
rs139214499 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17648581 | TGGCTTCATTCTTGA[C/T]GTCAGCGAGACCACA | 8027 |
rs139260110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678422 | TGTGCCTGGCTAAGT[G/T]TTTGTATTTGTAGTA | 8027 |
rs139263168 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716171 | ACGGAAAAGTTGAGT[C/T]GAACATCATATTTAA | 8027 |
rs139303969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17665572 | ATCCTGTCAGTCTTA[A/G]AAATGTATTTCTTTT | 8027 |
rs139307329 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17679868 | TTATCCAATTTGTTG[A/G]CATAAAGTTGTTCAT | 8027 |
rs139331510 | snp | C/T | 0.00057662 | 0.0169699 | missense | STAM | GRCh38.p7 | 10:17708900 | AGGCAGTGGTCCCAC[C/T]ATCCGCAAACCCAGC | 8027 |
rs139405849 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17659768 | CTGCCTAGCCTCTAA[G/T]GCTGTTTTTTTCTTT | 8027 |
rs139477610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17659209 | CCACTTCATGTGTAA[C/T]GCAAGTACCTTATAA | 8027 |
rs139648467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17679528 | CTTTTCTTTATTGAT[A/G]GTATCCCTTAATGCA | 8027 |
rs139693425 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17668640 | CTTCCTCTCTTTGCA[C/T]TTTAAACAGCCACTG | 8027 |
rs139699070 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695718 | ACTATAGCTTTGTGA[C/T]GTTTTACTTGAAAAT | 8027 |
rs139803709 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17671968 | CCTTTAGAGTATACA[A/G]TCTTCCTGTCACTGC | 8027 |
rs139863559 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680483 | GCTGGAGTTCAGTGG[C/G/T]GCAATCGTGGCTCAC | 8027 |
rs139883832 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17683219 | CTCAGGATGGAGTAC[A/G]GTGGTGCCATCACAG | 8027 |
rs139897219 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17676230 | CAGGCATGAGCTGAC[G/T]TATTTTTAATAGTTA | 8027 |
rs139931071 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17648947 | CAGGCTTCTTAAATC[G/T]GAACGCTCCAAGCTC | 8027 |
rs139950425 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17652757 | CATGCTTTCCTTTTC[C/T]AAGATGAAGTAAGTG | 8027 |
rs139969080 | in-del | -/A | 0.492823 | 0.0594727 | intron-variant | STAM | GRCh38.p7 | 10:17649394 | TGAGACCCTGTCTTT[-/A]AAAAAAAAAAAAAAA | 8027 |
rs139982489 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690174 | GAACTAGAACACAGG[A/C]ATGCTGATTCTCAGT | 8027 |
rs139990029 | in-del | -/AG | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715384 | CTAATTGTGAGCTAA[-/AG]AGAGATATATATATA | 8027 |
rs140058206 | snp | A/C | 3.31274e-05 | 0.00406972 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660544 | GTTGGTCAGTCTCGC[A/C]CTGGGTAAGTATTTA | 8027 |
rs140076681 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696616 | ACCTTTTCTGAGGCT[G/T]CTTCTTCTTTTGTAA | 8027 |
rs140097194 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17699559 | TGTTGATCCCTCAAT[A/G]ACCACTTTTTAATGT | 8027 |
rs140097300 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17660123 | TAAAGATTTACTAGC[A/G]AGTAAATAATCTTTT | 8027 |
rs140097705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646849 | TCACCATATCTACCA[A/G]TGAATATGTCATAAC | 8027 |
rs140104947 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17669811 | CACACCGTTCTCCTG[C/T]CTCAGCCTCCCCAGT | 8027 |
rs140142261 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17665122 | TGTGAAGTTTCATTT[A/C]GTCAGAACTGTGACC | 8027 |
rs140207588 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17705136 | ATTGTGGAGGAACCA[A/C]CTCTCATTCACATAT | 8027 |
rs140258854 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | STAM | GRCh38.p7 | 10:17686295 | CATTTCCAAAAACGA[C/T]TTCCTATAGGCAAGA | 8027 |
rs140275302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17673373 | CTAAATATTAGTTGT[A/G]CAATAGTGAAAAGCA | 8027 |
rs140297088 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642641 | TGCCATGTATACCTT[G/T]GTTCATGTTTTAAAA | 8027 |
rs140298167 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688850 | GCTATAATTTTCTAC[A/G/T]AAGAATGATAGCTCA | 8027 |
rs140382117 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17692085 | TAGGCTGTGAGGTGC[C/T]CATGAGGTGTAGGTG | 8027 |
rs140389518 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656293 | AGCGAGACTCCGTCT[C/T]AAAAAAAAAAAAAAA | 8027 |
rs140415936 | in-del | -/C | 0.157311 | 0.232183 | intron-variant | STAM | GRCh38.p7 | 10:17674014 | GCGGGAGAGTCCTTG[-/C]GAGGGACTGGAGGTC | 8027 |
rs140477116 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17658231 | TTAAAAGTGTGTTAG[G/T]CTCCATGTACTTTGG | 8027 |
rs140486720 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17687115 | TTCTTTAATACGGAA[G/T]AATAATGCCCTGCAC | 8027 |
rs140532472 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | STAM | GRCh38.p7 | 10:17654587 | CATATTGCAGATACA[A/T]GAGTAGTCTTATCAT | 8027 |
rs140639291 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17650396 | ACCAGAGTTGAATAG[C/G]CTTCAAATATCTCAA | 8027 |
rs140657702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17713175 | TCTGCCTCACCGCCA[C/T]TTCTTCTCAGCCTCA | 8027 |
rs140733192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645264 | GAAAGCAAGCCAAAT[A/G]CCATTTCCAAATCCC | 8027 |
rs140735367 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17706701 | ATATTTTTAAAGCTT[C/T]GTATGTAATTATTTA | 8027 |
rs140770039 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | STAM | GRCh38.p7 | 10:17674735 | GATGTCACCTCTTGA[A/G]GGGAAATGGTAAGTT | 8027 |
rs140808898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677577 | ACTGTGAAAAAGGCA[A/G]AATCTAAATAATAGT | 8027 |
rs140833218 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17673023 | TTTTAAAATACCAAA[A/G]TGGGGTTTTAAGAAG | 8027 |
rs140900486 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643669 | GACACGCGCGCCCTG[A/G]ACACTCCCCTCTTGG | 8027 |
rs140991080 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714635 | CTGCTGCTGCAACTG[C/T]CGATGTCACTCTGTA | 8027 |
rs141027884 | snp | A/G | 0.000310211 | 0.0124503 | intron-variant | STAM | GRCh38.p7 | 10:17684935 | TAAATAAGGTAAGGA[A/G]CATTATTTCCAGAAA | 8027 |
rs141055987 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17656738 | CAATCTCAGTTCTTG[C/T]CTCCTCAGAAGAAAG | 8027 |
rs141191429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687673 | TTGGAATAAAGGAAC[C/T]GTATCATTTATTCTC | 8027 |
rs141213232 | snp | C/G/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698093 | AGAAGGCTTGAACAG[C/G/T]AAACCAGAAATTACA | 8027 |
rs141228141 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17655201 | TTTCCTTTCTTAGAT[C/T]GTAAGCTACTTCTGG | 8027 |
rs141228467 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | STAM | GRCh38.p7 | 10:17691086 | TATTTCTGACCAGGC[A/G]TACCTGTAGTTTTCA | 8027 |
rs141233759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685752 | GGGACAAGGCACTCT[A/G]TTTTTCTATTGGGAC | 8027 |
rs141297110 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | STAM | GRCh38.p7 | 10:17657608 | TGTGCTTTCTGTTTT[A/G]GAAGATTATTAATTA | 8027 |
rs141344302 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17666507 | TCACCCCATTCTCCC[A/G]CCTCAGCCTCCTGAG | 8027 |
rs141388773 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | STAM | GRCh38.p7 | 10:17682178 | TTATGCAAGTACTAA[G/T]ATGCATTGTCACTAT | 8027 |
rs141435638 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17669008 | ATCATATGGTAAGAC[C/T]GTTTATCTTTGTTAG | 8027 |
rs141437027 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17648524 | CTCACTCTTTGGGTC[C/T]GTGCTACCTTTAAGA | 8027 |
rs141534466 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666760 | CCTTCAGTAGGAAGT[-/T]GAAAGAATATTTCCT | 8027 |
rs141637385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714336 | AACTTTTTTTACACA[A/G]TGGTTAAATAACACA | 8027 |
rs141671460 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17667018 | GTTTGATTATCACAG[A/C]AGTTCTAGGTACTGT | 8027 |
rs141685005 | in-del | -/TTA | | | intron-variant | STAM | GRCh38.p7 | 10:17654214 | AACCAGGTATTATTG[-/TTA]TTATTATTATTATTA | 8027 |
rs141695110 | snp | A/T | 1.6513e-05 | 0.00287336 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660516 | GGGCCTCATTTTGGA[A/T]ATCTGTGATAAAGTT | 8027 |
rs141738169 | snp | A/G | 0.000823303 | 0.0202725 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714679 | CCTAATATGCCCCAG[A/G]TGCCAAACTATAACT | 8027 |
rs141762419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681271 | TTACTACACCCTTAA[A/G]TTTTCTTGGGTTATG | 8027 |
rs141778604 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | STAM | GRCh38.p7 | 10:17695159 | GAAGGCCGAAAAGTT[C/T]GTGCTATATATGACT | 8027 |
rs141797154 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715635 | AATGATGTTGGTTTA[A/C]CTTTTCCTAGTTGAA | 8027 |
rs141823797 | snp | A/G | 0.00253431 | 0.0355068 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714786 | TCTGCTATAGGACCC[A/G]GTGTTCCTCTTGGTG | 8027 |
rs141831181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655526 | TGATGCTGTGATATA[C/T]AGCAGGTATTATACA | 8027 |
rs141857536 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17684058 | GATGCTTCACTGTGG[C/T]CTCATCTCTGACGAC | 8027 |
rs141868352 | snp | C/T | 0.000164804 | 0.00907607 | synonymous-codon | STAM | GRCh38.p7 | 10:17705645 | GGCCCTTTCCTTATA[C/T]ACCAAGTTAATGAAC | 8027 |
rs141931235 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17709368 | TCTCTTTAAGACAAA[C/T]ATTTTCTTATTTTTG | 8027 |
rs141967323 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17675619 | TTAACTTATACAGGG[A/T]TTCACTTAAGTTTTA | 8027 |
rs141996629 | in-del | -/A | 0.0372196 | 0.131242 | intron-variant | STAM | GRCh38.p7 | 10:17667916 | AAGTCAGTTGCCCTG[-/A]ATGAGCGCAGAGCTG | 8027 |
rs142002104 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | STAM | GRCh38.p7 | 10:17664992 | AAATGAAATAATTCA[C/T]ATTATTTTAACCTTT | 8027 |
rs142076577 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17680865 | GCTTATCCATTTATG[C/T]GTCTGTGGACACTTG | 8027 |
rs142179894 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17677078 | GTTTGCACAAACAAG[A/G]TGTTCATCAGCGCTT | 8027 |
rs142190246 | in-del | -/AAGAG | 0.157972 | 0.232445 | intron-variant | STAM | GRCh38.p7 | 10:17672867 | CATTTATCAAATGAT[-/AAGAG]AAGTAGGTATTTTTA | 8027 |
rs142207853 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697298 | CATTAAGAAGTCTTA[C/T]AGAATTTATACATTA | 8027 |
rs142228307 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17670232 | CCTAGACAATGATTT[C/T]ACTTTTTTATTTTAC | 8027 |
rs142273095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17700466 | AGTCCTTTGTTTGCC[A/G]TGCCAGAGCCTCATT | 8027 |
rs142351284 | in-del | -/GTT | | | intron-variant | STAM | GRCh38.p7 | 10:17706241 | TTTTTTGTTGTTGTT[-/GTT]GTTTAAAGGAAATAG | 8027 |
rs142360622 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17699697 | TAAACGCCTACGTGG[C/T]ACGCCAGATAATACA | 8027 |
rs142398393 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17686968 | TCTTTATATCTATTA[C/G]ATCAAATAGTAAGAC | 8027 |
rs142445923 | in-del | -/T | 0.184838 | 0.241358 | intron-variant | STAM | GRCh38.p7 | 10:17693890 | TTTGTTAAATGGTTG[-/T]TATGATTTCCTTTTC | 8027 |
rs142468853 | in-del | -/C | 0.172351 | 0.237636 | intron-variant | STAM | GRCh38.p7 | 10:17658528 | ACCTGTCCATTTCTT[-/C]TTTTTTTGGTCTTGC | 8027 |
rs142490294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683913 | TTAAGGAGTATTGGA[C/G]TTTATTTTTTCAGAA | 8027 |
rs142507886 | in-del | -/C | 0.466824 | 0.124448 | intron-variant | STAM | GRCh38.p7 | 10:17661908 | TGTGGTCCCATCCAT[-/C]CCCTTTGTTGTATTT | 8027 |
rs142573207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713890 | TTGTGGCCATCAGGT[A/G]CTGTGTGTTCTCCAG | 8027 |
rs142610825 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17682529 | TTAGATATTTGTTAT[G/T]TGATTTCCAAATATT | 8027 |
rs142632711 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | STAM | GRCh38.p7 | 10:17654246 | TATTATTTTTGAGAC[A/G]GAGGCTTGCTCTGTC | 8027 |
rs142640288 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17707236 | AACATGGTGAAACCC[C/T]GTCTCTGCTCAAAAT | 8027 |
rs142641038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646395 | CTCCCAGTTGAGAAC[C/T]GCTGCACTAGTCCAC | 8027 |
rs142649161 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17685494 | AAAGAGGCACTAAAT[C/G]CCAGGGTGATCAGTC | 8027 |
rs142674086 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688940 | TTATGAATTCCTCTA[G/T]TAACAATGAGAGGAC | 8027 |
rs142692625 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697108 | GTGTGTATGTATTTT[A/T]AGTAGAGACAGGGTT | 8027 |
rs142702613 | in-del | -/TATT | 0.136506 | 0.222754 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697722 | TCATAATCTCCCCTC[-/TATT]TAGGAAAACAGAAAA | 8027 |
rs142743724 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17658925 | ATGCAGACCATTGAC[A/C]TGTAAAGTGACTGTT | 8027 |
rs142789591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661994 | TGTGTGTTACATATC[A/G]CGTTCCCTTTTCTCC | 8027 |
rs142836471 | snp | C/G/T | 6.61441e-05 | 0.00575045 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688058 | GTGAAAAATTAAAGG[C/G/T]TCTTATGGTTGAATG | 8027 |
rs142903210 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | STAM | GRCh38.p7 | 10:17657049 | ATGCATGCCCATCGG[A/G]GGCTTTTTTCCCTTT | 8027 |
rs142947051 | snp | C/G | 0.000905596 | 0.0212598 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714709 | TTAACATCATCAACT[C/G]TGCCTCAGCCCGGAG | 8027 |
rs142963014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17706751 | CATCAGGTTGTGTAC[A/G]CTCAATATGTATAGC | 8027 |
rs143008089 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17699021 | AATTAAGCTATTTCT[A/G/T]TGTTATACAGAAGCA | 8027 |
rs143028570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17710184 | GTCCTCTGTTTGACT[A/G]TGTCACATGCTGCTC | 8027 |
rs143028815 | snp | A/G | 4.94319e-05 | 0.00497127 | missense | STAM | GRCh38.p7 | 10:17704465 | TACAGATGCTGCAAA[A/G]TACAGACCCCAGTGA | 8027 |
rs143048946 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17701317 | TTCTACTCAAACTTA[A/T]TACCATGTTTTAAAA | 8027 |
rs143091558 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17669622 | AATGTTTCGTCTGAG[A/G]TATTTTGTCCTTTTT | 8027 |
rs143094182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17676088 | CTTCAAGTTCTGCAG[A/G]GTTTGTGTTTTGTTT | 8027 |
rs143270243 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17681867 | AGTCCTTTGCTTATT[A/G]TATAATTTTTGAGAG | 8027 |
rs143270495 | snp | G/T | 0.021333 | 0.101051 | intron-variant | STAM | GRCh38.p7 | 10:17708162 | CCCAAAGTGCTGGGA[G/T]TACAGGCATGAGCCA | 8027 |
rs143287199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17646835 | AACAATTTTTTCTTT[C/T]ACCATATCTACCAAT | 8027 |
rs143327000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17649029 | CAGGTATTTGAAGGT[C/T]TGGATATTCATCACA | 8027 |
rs143360720 | snp | C/T | 0.115788 | 0.21092 | intron-variant | STAM | GRCh38.p7 | 10:17678366 | TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCTGG | 8027 |
rs143405217 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644045 | CAGGCAGAGGGGACT[C/T]CCTGTTCAGCCTTTA | 8027 |
rs143551071 | snp | A/C | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688573 | GTTCAGGTGATTCTC[A/C]TGCCGCAGCCTCCTG | 8027 |
rs143650239 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17660688 | CCCAGGAGTTAGAGG[C/T]TGCAGTGTGTGATGA | 8027 |
rs143674279 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17651804 | ATTGGCCATTTTTAA[C/T]GAACTGTTACATCTT | 8027 |
rs143687586 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714405 | AATAACAATGTTTGG[C/T]ACATTATAGCTGTTT | 8027 |
rs143704745 | in-del | -/AT | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17681604 | TGTTATTAGAGGAAA[-/AT]ATATGTCATTTTAAT | 8027 |
rs143754165 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17665465 | CAAATGTGAATACAT[A/T]TTCCCCCCATTTACA | 8027 |
rs143788069 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17676334 | AGAGGAGCTCCATCT[C/T]AAATCTCCTTTCTTT | 8027 |
rs143796756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709145 | TGGTCCTCTGCTCCC[A/G]ACTCGCTCAACTCAT | 8027 |
rs143871558 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17663653 | TTAAGTTAATCTTCA[A/G]GCATTTATTGTGTGC | 8027 |
rs143879916 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17679179 | ATTTTACATTCCCAC[C/T]GGCAATGTACAAGGG | 8027 |
rs143902989 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645031 | AGTTGTTGAATCTGG[A/C]AAGAGTTTGAAATGC | 8027 |
rs143935560 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716497 | CACATTTTAAATACT[A/G]TAAGTTAGTTTTTGA | 8027 |
rs143962408 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | STAM | GRCh38.p7 | 10:17648405 | CGGGGACAAATAAGA[G/T]AATAAAAGCTGGGCA | 8027 |
rs144011429 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712763 | AAGACAGGAAGTAGA[C/G]GCAGTGGATAAAGAC | 8027 |
rs144052853 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17677391 | CTAAAATATTGAGCT[A/G]AATCATCTTTAGATT | 8027 |
rs144074759 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17679952 | TTTGTTTTTTGATTC[C/T]AATAAATTGAGTCAC | 8027 |
rs144091446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17711122 | TGTTGTTGTTTTTGG[C/T]AGGCAGGTTTTTTAG | 8027 |
rs144156282 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17676557 | TCTTTTACCCTCTTA[A/C]GAACTATATGACCCA | 8027 |
rs144157298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654025 | AAGTGCCTGGGGACC[C/T]CAGAGCTTGTGTCTG | 8027 |
rs144248717 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17656427 | TTTAACTTCACTGTA[A/G]GTTGGTCTGGTGGGC | 8027 |
rs144291199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671214 | TCCAATATAGACGTA[C/T]ATATGTCCTTGAATG | 8027 |
rs144318725 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690841 | GTAGGCTAGCAGCAC[C/G/T]GCTACCGTAGTTGGC | 8027 |
rs144359634 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696112 | TGCTTTGGGGGTTAG[A/G]ATTTCAACCTGTGAA | 8027 |
rs144430312 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17693720 | TTTCTGTCTTCCTAC[C/T]GATGGACCTGTGGAT | 8027 |
rs144521118 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17703198 | TCATTTGACCTTTTT[C/T]TGTGTGTGGTAGGCA | 8027 |
rs144585358 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17679685 | TGGGAAGTTTTCTTA[A/T]TCAGTAATTTAGTCT | 8027 |
rs144616585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645757 | ACACTACAGGACACA[A/G]CAGCTCAGTGACATA | 8027 |
rs144619071 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643740 | GCAAGTTTGTCACCT[A/C]ACGCAGCTAATTAAA | 8027 |
rs144625709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704329 | AAAATTGGAGTCTCC[A/G]TAACTATGAATTTCA | 8027 |
rs144666693 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17671585 | TCCCATGACAGGCGG[A/G]TTACTACTGATGTTA | 8027 |
rs144752574 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17702585 | TATGTGAAGGGGTTT[A/G]TGGGCTTTTAGCAAT | 8027 |
rs144823642 | in-del | -/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715502 | TTTTTGGTGCAATTA[-/T]TAGCAAATGATAATG | 8027 |
rs144845489 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | STAM | GRCh38.p7 | 10:17698865 | ATGCAGTGCTATCCC[A/G]GCTTTCTACTTGTAA | 8027 |
rs144852125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17654291 | GCAGTGGCATGATCT[C/T]AGCTCACTGCAAGCT | 8027 |
rs144863714 | snp | C/G | 0.0119091 | 0.0762411 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717292 | TGCTTGAACCTGGGA[C/G]ACGGAGGTTGCAGTG | 8027 |
rs144887203 | snp | A/G | 0.000105489 | 0.00726177 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688224 | TTGTTTCTCTTAAAT[A/G]GCTATATTTATTTGA | 8027 |
rs144950713 | snp | A/G/T | 0.00100435 | 0.022387 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714663 | GTACCAGAATGCAGG[A/G/T]CCTAATATGCCCCAG | 8027 |
rs144961515 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17703595 | AAAAAACATAAATAC[A/G]TATATACTTATATAT | 8027 |
rs144977679 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17655324 | CATGAATTGTTTGGA[C/T]CTTTGTATTAATTCT | 8027 |
rs144979548 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | STAM | GRCh38.p7 | 10:17691337 | TCCTGGCTAACATGG[C/T]GAAAACCTGTCTCTA | 8027 |
rs144993174 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17669178 | CCAACACCATTTACT[G/T]AATCGTCCATCTTTT | 8027 |
rs144997868 | in-del | -/CACT | 0.0134861 | 0.0810011 | intron-variant | STAM | GRCh38.p7 | 10:17674925 | TTTTGATACTTGAGA[-/CACT]CAATCCTTAAGAATG | 8027 |
rs145017756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17657704 | GATTATGTCTTTCAA[A/G]GCATTGGTCCATTTC | 8027 |
rs145072892 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17704848 | AGACTAAGGTTAAAG[-/A]ATGTATATTTTTATT | 8027 |
rs145172271 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17705390 | ATAAGACGGAGTTCC[C/T]TTAGCACAGCACGTA | 8027 |
rs145177978 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17665786 | AGTTTCTTTTTAAAT[C/G]TTGAAATACTTGATT | 8027 |
rs145179086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703622 | ATATCGTATAGATGT[G/T]TGTATGTAATAATGG | 8027 |
rs145220060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17708291 | AACTTAAAATATTTA[C/T]GTCAGGCCCTTTACA | 8027 |
rs145280352 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673675 | AAGGAGAAAAACCCC[G/T]CAAACCAACCCAACA | 8027 |
rs145389186 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713739 | GGTCGGCTCTCTCCT[G/T]GTGGATCGTAATAAC | 8027 |
rs145432814 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | STAM | GRCh38.p7 | 10:17677797 | AGCAGCCTCACAGGC[A/G]GTTGAGCATCCTTAA | 8027 |
rs145588348 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17684306 | AAAAAGTTAACCTCA[A/G]TGTGGAAAATCTGTT | 8027 |
rs145636613 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17685451 | CTGCCCCAAACTGTT[A/C]CAGATAGGGCCAGAT | 8027 |
rs145656744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17687339 | AATTAGCTGGGCATG[A/G]TGGTGCGCGCCTGTA | 8027 |
rs145702558 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696982 | TGGAGTGCAGTGGTG[C/T]GAGCTCGGATCATTG | 8027 |
rs145721992 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700601 | ATTTTTTTTTTTTTT[-/T]GAACATCTATCTTTG | 8027 |
rs145749574 | in-del | -/T | 0.176861 | 0.239062 | intron-variant | STAM | GRCh38.p7 | 10:17658198 | AAAATTTCTTTTAAG[-/T]TTTTTTTTTACTCTT | 8027 |
rs145776213 | snp | A/G/T | 0.000708495 | 0.0188084 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684730 | CACAAAGATCCTCAC[A/G/T]TTGCTATGCAGGCTT | 8027 |
rs145804938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17690256 | GAATATGTGTCTGTC[C/T]AGACCAGGCTTCCAG | 8027 |
rs145850510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656907 | AAGTGCGGTTTTTAA[C/G]TTTGATCCCAGGACT | 8027 |
rs145879188 | snp | C/T | 0.00558195 | 0.052534 | intron-variant | STAM | GRCh38.p7 | 10:17693328 | GTGCGTTTTTAAGTC[C/T]CTGATGGTGGGAATA | 8027 |
rs145888338 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17647652 | ATAATCTGTGTCTCA[A/G]TTTCCTTATCTTTAA | 8027 |
rs145891108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17708637 | TTTTTCAAAATGCCC[A/G]TTGACAGAAATAACT | 8027 |
rs145896860 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17675109 | CTGATTAGGTAGTCA[G/T]GAAGATTTTCTTTCA | 8027 |
rs145943446 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697513 | GTTTGATTTACAAAC[C/G]CTGCTGAGTAGGATA | 8027 |
rs145992840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17682906 | CTTTATATATTTTGA[A/G]GTTCTATTTTTGTGT | 8027 |
rs146020314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648871 | TTATTGTGGCTCACA[A/G]TATGGCTTCTTCCTG | 8027 |
rs146104659 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696303 | TTTACACCTAGGAGT[A/G]TACTCTTTGCGAATG | 8027 |
rs146115732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699245 | ATCTCATAAGATTGG[G/T]AGATTCATTGGAGGA | 8027 |
rs146140346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701414 | TTGAAGTGTCACATT[G/T]TATAGATCAGGAGTT | 8027 |
rs146143614 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17665102 | GGGGAGAAAAGAGCT[A/G]TTATTGTGAAGTTTC | 8027 |
rs146222635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711740 | CCAAGGGTTGAAAGC[A/G]TGTAGGGGAGCAGCG | 8027 |
rs146234865 | snp | A/G | 4.94319e-05 | 0.00497127 | synonymous-codon | STAM | GRCh38.p7 | 10:17705669 | AATGAACGAAGATCC[A/G]ATGTATTCCATGTAT | 8027 |
rs146242697 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17652918 | GATAAAATTCTCTTA[C/T]AGTGTTGAATGATAA | 8027 |
rs146245558 | snp | C/G/T | 9.92567e-05 | 0.00704416 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660539 | ATAAAGTTGGTCAGT[C/G/T]TCGCACTGGGTAAGT | 8027 |
rs146275641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682241 | ATGAAATAGTATTGT[C/T]AGTACTCCTGTGTCT | 8027 |
rs146439775 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17677495 | GTTTTGTGTTTTTAT[A/G]TCGGCATGGTATTCA | 8027 |
rs146465898 | snp | G/T | 0.0236746 | 0.106192 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642965 | ACGGGGTTTCACCAT[G/T]GCCAGGCTGGTCTTG | 8027 |
rs146465985 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17680038 | AAAAAACTTGTGTTC[A/G]TTGGCTTTTCTTGAT | 8027 |
rs146563746 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17691063 | AAATTTATGTAAACC[A/G]TAAAACTTATTTCTG | 8027 |
rs146581804 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17709519 | CCCATTTACTTTGCC[A/G]TTTACTTACAGTGCT | 8027 |
rs146601820 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17660095 | ATTAACTTAATTACC[C/T]GAAACATTTTTATAA | 8027 |
rs146667587 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | STAM | GRCh38.p7 | 10:17704719 | CAAACGAAGTGTTCT[A/G]TTCAACATTTTAGAA | 8027 |
rs146686028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17708243 | TTTACTGACAGAGCC[A/G]AGTAGTTGTGTCAGA | 8027 |
rs146687163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17646839 | ATTTTTTCTTTCACC[A/G]TATCTACCAATGAAT | 8027 |
rs146689436 | snp | A/T | 0.000153988 | 0.00877328 | missense | STAM | GRCh38.p7 | 10:17693289 | CTGTGGCTAACAAAA[A/T]AGAAGAAGAAGATTT | 8027 |
rs146697978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17649082 | CGTCATTTTCTGAGA[C/T]GCTTTACCTAATAAT | 8027 |
rs146718467 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713918 | CAGCCCCCTCCCCAC[C/T]ACCGCAGTCCTGCCG | 8027 |
rs146762231 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17685382 | TATTCTTACTGGCTG[-/A]ACCCACAGCTGGAGT | 8027 |
rs146828778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665534 | ACTTAATTACTTATC[A/G]TTACTTATTGACTAC | 8027 |
rs146952486 | snp | A/G | 1.64863e-05 | 0.00287104 | missense | STAM | GRCh38.p7 | 10:17695190 | TTGAAGCTGCTGAAG[A/G]CAATGAACTTACTTT | 8027 |
rs146957897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17662161 | GTTACTCCCCTACCT[C/T]CCATACTGAGTTCAG | 8027 |
rs146981291 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17666519 | CCCGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8027 |
rs147063208 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17705110 | CTATAACTGCCTTTT[-/A]AAAAAAAAATATTGT | 8027 |
rs147063533 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | STAM | GRCh38.p7 | 10:17678534 | GCTGGGATTATAGGC[A/G]TGAGTCACCACGCCC | 8027 |
rs147086613 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681379 | GGATGTTGATTTTCA[C/T]GTATTTTAATTTTCT | 8027 |
rs147096114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647911 | CCTTACTGAGCATCT[C/T]CATTTGGATTCTGCT | 8027 |
rs147119276 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17650527 | AACTTGGGAGTAATT[C/G]TTGACTTCTGTAGTT | 8027 |
rs147135123 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17686099 | GGTTAAATGATAATT[C/T]TTTCCCTTTCCTGCT | 8027 |
rs147158378 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688609 | CTGGGACTACATGCA[C/T]GTGCAGCCAGACCTG | 8027 |
rs147191676 | snp | A/G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669916 | TTTGTATTTTTAGTA[A/G/T]ACACGTGGTTTCACC | 8027 |
rs147259689 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17706631 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 8027 |
rs147262421 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645133 | TTTTTAATTTTATTT[A/T]ATTTTATTTTTTTCT | 8027 |
rs147346542 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | STAM | GRCh38.p7 | 10:17656515 | GTCTTTCCTCTTGGG[C/G]TGACATAGAGCCCCC | 8027 |
rs147369166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17659178 | TAATCCAAGTCTGCT[C/T]TCAGATAACACTGTA | 8027 |
rs147410383 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652248 | TATATCCTTCTGATT[A/T]AAAAAAAAATACTTG | 8027 |
rs147426407 | in-del | -/GTA | | | intron-variant | STAM | GRCh38.p7 | 10:17666385 | TTTTTCCTTGGCTTT[-/GTA]TTTTTTTTTTTTTTT | 8027 |
rs147436159 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | STAM | GRCh38.p7 | 10:17676682 | TGCTGTTCCTCTGTT[-/A]ATGTCCAGTTAACAC | 8027 |
rs147439988 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17707029 | ATGCAGTGTAGAGCC[C/G]TTTGCTTTCTTTTCA | 8027 |
rs147451957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671683 | CGTTTTTAGTCTGAC[A/G]TAGGTTATTAGAGGT | 8027 |
rs147456118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17710247 | TCATTCTTCAAGGTC[A/G]GGGCCTTGGGAAATT | 8027 |
rs147474748 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17676218 | TTCATTTACTTCCAG[A/G]CATGAGCTGACTTAT | 8027 |
rs147477282 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17680432 | TTTTTTTTTTTTTTT[-/C]TTTTTTTGGAGATAT | 8027 |
rs147615362 | in-del | -/T | 0.364609 | 0.222182 | intron-variant | STAM | GRCh38.p7 | 10:17659115 | TACTTTTTTAAAATC[-/T]TTTTTTTTTTAGTAA | 8027 |
rs147722912 | snp | C/T | 0.00123604 | 0.0248293 | intron-variant, synonymous-codon, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684855 | AGCATGTGTATCAAA[C/T]TGTGGCAAAATTTTT | 8027 |
rs147732763 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17650607 | AGATACCCTGGTACC[A/G]AATATGCCCTCAAGG | 8027 |
rs147755098 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17654055 | GAGGTTTGAAGTGAA[C/G]GGAGTCTTATGGAGA | 8027 |
rs147826707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17700681 | TTGTGTATTTTCCAT[G/T]TTAATAGATAATGTC | 8027 |