SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs79115102 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | BTRC | GRCh38.p7 | 10:101453870 | CAGATAATAAACATT[G/T]GAGGCTTTGTGGGAG | 8945 |
rs79131241 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | BTRC | GRCh38.p7 | 10:101369381 | TCATTATTTTTTGTG[C/T]GCCAGGACTCCTTAT | 8945 |
rs79177816 | snp | A/C | 0.494651 | 0.0514399 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553971 | CTGTGGCAACAGTGG[A/C]TTCTCAGACATGATA | 8945 |
rs79221235 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | BTRC | GRCh38.p7 | 10:101461455 | GAGGTGACAGTGCCA[A/G]GGAATGGACTCTAAT | 8945 |
rs79286367 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433795 | AGATATGTTACTCTG[A/G]CTATAAAAAGGATAA | 8945 |
rs79286598 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481562 | TATATGATGTGGAGT[G/T]TTTTTTTTTTAATTG | 8945 |
rs79322713 | snp | C/T | 0.0022514 | 0.0334759 | intron-variant | BTRC | GRCh38.p7 | 10:101550676 | AGTTCAAGTTCCTAC[C/T]CTTTTTGTTTCTACT | 8945 |
rs79341506 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442304 | TGTGTGTATGTGTGT[A/G]TGTGTGTGTGTGTGT | 8945 |
rs79359403 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101540606 | TGATTTTTCATGTTA[A/G]TTTTAAAATCAGTTT | 8945 |
rs79386471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537567 | TCACTTAGGAAGAAC[G/T]CTTATCATTTCTTTT | 8945 |
rs79394936 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | BTRC | GRCh38.p7 | 10:101536309 | TGTTTACAGAATTAT[G/T]TAAAGCCCTGTGCTT | 8945 |
rs79452197 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436255 | AAATGAGAATGAGCA[A/T]TAGAGTTAAAGTAAT | 8945 |
rs79471180 | snp | A/C | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101549267 | AAGACCTAATCTCTA[A/C]AAAAAAAAAAAAAAA | 8945 |
rs79528180 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | BTRC | GRCh38.p7 | 10:101458422 | TTCATTTTTTAATGG[C/T]GGTGTTATACAACTG | 8945 |
rs79553570 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502777 | TATTTTTGAGCTGCT[A/G]TTATATAGATACTGA | 8945 |
rs79563587 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101439856 | GGCAGGAAGTTGGGA[A/C]GGTGGTATTGGGTAA | 8945 |
rs79566347 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101395069 | AAAATTGTATCATCT[A/T]GTGTATAGCCTAGGA | 8945 |
rs79581511 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101522923 | TTAAATTCTACAGAT[G/T]GGTTGGGCACGGTGG | 8945 |
rs79678275 | snp | A/G | 0.375 | 0.216506 | intron-variant | BTRC | GRCh38.p7 | 10:101457312 | ATGCTACCTGCTTTA[A/G]GTGATCCTGGATTAT | 8945 |
rs79697378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390864 | CCCAAGCAGCTTCCA[A/G]ACACTTTAAGGAGGT | 8945 |
rs79733519 | snp | G/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101505933 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 8945 |
rs79744089 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101539682 | TTTTATTTCTCTGAG[G/T]TAAATACCTAGGAGC | 8945 |
rs79758656 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | BTRC | GRCh38.p7 | 10:101397976 | AAATTCCACTTGCTC[A/G]TCACAGCAAGATATT | 8945 |
rs79769745 | snp | A/C | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101421622 | CCCTCCCCCCTCCCC[A/C]CTCCCCCCACCCCAC | 8945 |
rs79798670 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101391997 | TATTCTTTTTTTTTT[G/T]GAGACGGAGGCTTGC | 8945 |
rs79829544 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101430262 | CAACTGGAATATTGC[A/G]TTCAGCCAAGCCTTA | 8945 |
rs79841609 | snp | G/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538326 | TCTTGTGGCTGCTTT[G/T]GACCCCCGTGCTCCT | 8945 |
rs79843468 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101502998 | AATACCTTTATATGT[A/G]TTATTTTAATCTTAA | 8945 |
rs79855966 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101475266 | GAAAAACAGCTGGGC[A/G]TGGTGGCTCACGCCT | 8945 |
rs79881746 | snp | C/T | 0.0139895 | 0.0824562 | intron-variant | BTRC | GRCh38.p7 | 10:101536521 | TACGTGAAAATTCAC[C/T]TGACTTAATTTTCTC | 8945 |
rs79931370 | snp | A/G | 0.14933 | 0.228835 | intron-variant | BTRC | GRCh38.p7 | 10:101394564 | CCTACTCCACAAAAT[A/G]CATAGTCACAGACTG | 8945 |
rs79971606 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | BTRC | GRCh38.p7 | 10:101475600 | TGGGGAGTTATATAT[A/C]TCTACTATTTTCCCC | 8945 |
rs80048478 | snp | A/G | 0.00528578 | 0.0511366 | intron-variant | BTRC | GRCh38.p7 | 10:101534952 | CCAACTTAGAATGGG[A/G]GAATTCATATGAAAA | 8945 |
rs80078543 | snp | A/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101438427 | GAGACTGCCTCAAAA[A/T]AAAAAAAAAAAAAAA | 8945 |
rs80092411 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101390021 | TATATCTCAGTTCTA[A/G]TCACCTACTTAGAGC | 8945 |
rs80100147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446592 | AACAGTTGATGCTGT[G/T]TATATTTCATTTTGT | 8945 |
rs80121027 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | BTRC | GRCh38.p7 | 10:101469918 | TGTTGCTGTGTATAT[C/T]AGTAGTTTATTCTCT | 8945 |
rs80126009 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101415955 | ACATGCTGTCCCTGC[C/T]TGTAGCACAGGAGCA | 8945 |
rs80151341 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101380203 | GCTTAACCTCCTTGA[A/G]TCTCACTTTCCTCAT | 8945 |
rs80235540 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | BTRC | GRCh38.p7 | 10:101401131 | TTGCAATGAGATTTG[A/G]CTTGAATTTAATACA | 8945 |
rs80272118 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101429512 | TCTCCCCYCCCCCCC[C/T]CCCCTCCCTCCCTTC | 8945 |
rs80321721 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | BTRC | GRCh38.p7 | 10:101364280 | AGATTTCTTCTCTTC[A/G]TGTTATGTAGAAAAA | 8945 |
rs80328017 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101372983 | ACACTATTGAGTTTC[A/T]TAGTCCACAAAAATG | 8945 |
rs80329794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101386528 | CACTTTGGCCAGAAA[A/G]CCTGGTTTGGATTTT | 8945 |
rs80348629 | snp | A/C | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101549269 | GACCTAATCTCTACA[A/C]AAAAAAAAAAAAAAA | 8945 |
rs111278549 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101370753 | TTTTTTGCATTTTTA[A/G/T]TGGAGATGAGGTTTC | 8945 |
rs111288882 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101527757 | AGACCCTGTCTCTTT[A/C]TCTGTCTCTCTCTCT | 8945 |
rs111314792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498145 | GCCCAGAGCCTTTTA[A/G]CCTGGCTTTCTTAAG | 8945 |
rs111324240 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101510441 | CGTGAACCCAGGAGT[G/T]GGAGCTTGCAGTGAG | 8945 |
rs111355116 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101471551 | TTTTCTTTTTTAAGT[A/G]TTTGCCAGGTTTTGG | 8945 |
rs111369711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101494201 | GACATAATGCAAAAC[C/T]AAACTAAGGTGGTAA | 8945 |
rs111374164 | in-del | -/TACAGGCA | 0.376592 | 0.215579 | intron-variant | BTRC | GRCh38.p7 | 10:101378797 | CCAAAGTGCTAGAAT[-/TACAGGCA]TTGAACCACTGTGCC | 8945 |
rs111381527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101411941 | TTTTAAGCTTTATTC[C/T]GATAGTTTTAGTGTA | 8945 |
rs111435252 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101363957 | ATCTTACAGTGATAG[G/T]TATTTATTCTCTTGA | 8945 |
rs111466110 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101531108 | CCCAGGAAGCGGAGG[C/T]TGCAGTGAGCCAACA | 8945 |
rs111501967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101538427 | GGGGAAGAAATTAAA[C/T]GTTGATGTGCTGTGG | 8945 |
rs111522268 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101396879 | ATGATCTTGGCTCAC[C/G]GGAACCTCCGCCTCC | 8945 |
rs111528460 | snp | A/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101374786 | TTAAAGTATAATAAA[A/T]AAAAAAAAAAAAAAG | 8945 |
rs111552991 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101413657 | GAAGATGTCCCAGAG[A/G]AAATCTTTACATTAA | 8945 |
rs111557096 | snp | A/C/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101442296 | TCTGTCTCTGTGTGT[A/C/G]TGTGTGTGTGTGTGT | 8945 |
rs111571439 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101499922 | CACTTGATGGACTTT[C/T]GAATCTGAAAGAAAA | 8945 |
rs111579762 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | BTRC | GRCh38.p7 | 10:101534930 | TAAGGCATTTTTCAG[C/T]AAGTTTCCAACTTAG | 8945 |
rs111616045 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101393264 | TTTGTATTCTTTGCA[A/G]TATCCTTCATAATAA | 8945 |
rs111653217 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101371235 | TGTTGCCCAGACTGG[A/G]GTGCAATGAATGGCA | 8945 |
rs111689841 | in-del | -/TTTG | 0.392881 | 0.205147 | intron-variant | BTRC | GRCh38.p7 | 10:101520135 | TTGTTTGTTTGTTTG[-/TTTG]GGGGGACAGAGTCTC | 8945 |
rs111696383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101537431 | TACTTAGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 8945 |
rs111711487 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353329 | TTTATTTGCTGGAGG[C/T]CATTATATTCCACCG | 8945 |
rs111733093 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441707 | TAGCATGGTGAAACC[C/G]AGTCACTACTAAAAA | 8945 |
rs111734784 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101497134 | TTCCAGTGTGATACC[A/C]AGTTGACCTAGCACC | 8945 |
rs111734903 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101397056 | TGATCCACTCGCCTC[A/G]GCCTCCCAAAGTGCT | 8945 |
rs111745322 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101437841 | ATACCGTTCTGCTTA[C/T]CTGAAAAAACCCCTC | 8945 |
rs111798179 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101466085 | TACTTTTTGAAAATT[A/G]TGGCATTACAACGTT | 8945 |
rs111823729 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101429810 | AAACATACGCAAACT[C/G]TGCAGAGTTTGTTGC | 8945 |
rs111851768 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101521580 | TACCAGAAAATCATA[C/T]ATATTTCCCTCATTT | 8945 |
rs111914920 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101444850 | CCTTTCTCAAGAGCA[C/T]GGCTGTAAGTGCACA | 8945 |
rs111918107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469726 | ACTATAGAATATTTT[C/T]ATAACCTAGGAATGT | 8945 |
rs111921065 | snp | C/T | 0.10237 | 0.201756 | intron-variant | BTRC | GRCh38.p7 | 10:101375342 | CCCTTTGCCTTCTCC[C/T]GTGATTTTAAGTTTC | 8945 |
rs111923824 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101459802 | TGATAAAATAGAGGG[C/T]CAGTAAAAAGAAAAT | 8945 |
rs112007824 | snp | C/T | 3.35267e-05 | 0.00409417 | intron-variant | BTRC | GRCh38.p7 | 10:101430482 | TCTGTGGGTTATTTG[C/T]GGGCATTAGTGTATG | 8945 |
rs112014779 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | BTRC | GRCh38.p7 | 10:101390423 | GCTCACTGCAAGCTT[C/G]GCCTCCCGGGTTCAC | 8945 |
rs112050586 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547334 | ATGGTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 8945 |
rs112063076 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101415669 | GCCTCAACCTTCTGA[A/G]TAGCTGGGATTACAG | 8945 |
rs112106179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101506292 | GAAGCCATCAGCTCA[C/T]TGGCACTATTGTAGC | 8945 |
rs112173179 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101424310 | AGATATGATTATCCT[A/G]TCTGACAGGTGGGAG | 8945 |
rs112193452 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101552883 | GAAAGCTATGCCAAC[C/T]GTGGGCACTCTCAGC | 8945 |
rs112203255 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101386020 | GTGTCAGGAAAAATG[A/G]TACAGAGATGACTTG | 8945 |
rs112238815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494534 | ATTGAGCAAGACATA[A/G]TTATCTTCCCTAAAA | 8945 |
rs112244338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101447047 | TGCAGCTAGTGTTCG[C/T]GTGCAGGTTGGACTT | 8945 |
rs112255681 | snp | A/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101482568 | GCCCGGCTAATTTTT[A/T]GTATTTTTAGTAGAG | 8945 |
rs112264573 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101387687 | GCCCACCACCACACC[C/T]GGCTGATTTTTTTTT | 8945 |
rs112270870 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101533338 | TTTCTTATCCTTATG[A/G]TAAACTTTGCATTCC | 8945 |
rs112299503 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101354658 | GGGGAAGGGAGCGCG[C/G]GATAGAGTGAAGACA | 8945 |
rs112317421 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101386195 | TATTATTCTACTGAT[A/G]TTTCCAGGACCTTTC | 8945 |
rs112345974 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101482353 | TTTACATGTGTTTTG[G/T]GTGTCTCATGATCCC | 8945 |
rs112348674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101452577 | GTCGGACAGTGTGGC[A/G]GGGAGAAAGCCTGCT | 8945 |
rs112368663 | snp | C/G | 0.383632 | 0.211288 | intron-variant | BTRC | GRCh38.p7 | 10:101505437 | ATCCTGGTTAACACG[C/G]TGAAACCCCGTCTCT | 8945 |
rs112443786 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | BTRC | GRCh38.p7 | 10:101441650 | TGTGGGAGGCTGAGG[C/G]GGGCGGATTGCCTGA | 8945 |
rs112455252 | snp | A/G | 0.386504 | 0.209444 | intron-variant | BTRC | GRCh38.p7 | 10:101505517 | CCCAGCTGCTCAGGA[A/G]GCTGAGGCAGGAGAA | 8945 |
rs112478635 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | BTRC | GRCh38.p7 | 10:101520051 | AATTTTGCCTACCAC[A/G]ATAACATACTTTTTT | 8945 |
rs112498195 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101462212 | ACTTTCAATCAGGTG[A/G]CATGGTTTTCCCAGT | 8945 |
rs112501825 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101464019 | TACAATTTTAACTGT[C/T]TGGAGAATCAACACC | 8945 |
rs112504877 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101474359 | GAATCTAAACTCATG[A/G]TCTCTTTGAATTTTT | 8945 |
rs112506533 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101437608 | TTCTGAATTTCACCT[A/G]TATCATATTGCTCAA | 8945 |
rs112511307 | snp | C/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101459352 | TCATTACCCCTTACC[C/G]TCAAGACTGTAGACC | 8945 |
rs112519582 | snp | A/C | 0.208169 | 0.246476 | intron-variant | BTRC | GRCh38.p7 | 10:101531642 | AGGAGAATCACTTGA[A/C]CCTGGGAGGCACATG | 8945 |
rs112543709 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532752 | GTACTGAAGCTATAT[A/G]TGTGTGTGTGTGTGT | 8945 |
rs112559738 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | BTRC | GRCh38.p7 | 10:101531002 | ACATGGTGAAACCCC[A/T]TCTCTACTAAAATAC | 8945 |
rs112582604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101407944 | GGCCAGGATGGCCTC[A/G]ATCTCTTGACCTCAT | 8945 |
rs112641804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101524641 | AATGATCAGGAACAA[C/T]TTGATGGCACCCATT | 8945 |
rs112651650 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101532776 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGC | 8945 |
rs112716867 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101411543 | TCCTCGGGTTCACTG[A/G]TCTTCTACAGAGTTT | 8945 |
rs112718993 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101477790 | GAGTAGCTGGAACTA[C/T]AGGCACCCACCACCA | 8945 |
rs112744139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101423997 | CACTTTGGGAGGCCA[A/G]GGCAGGTGGATCACC | 8945 |
rs112805242 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101458058 | CTAAATGTTTCAGTG[A/C/T]GTGTTTCCAGAAAAA | 8945 |
rs112821921 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101482551 | TAGGCGCCCGCCACC[A/T]CGCCCGGCTAATTTT | 8945 |
rs112851035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101486990 | TAGGATTAGTAATCA[A/G]TCTTATTGAAACATT | 8945 |
rs112864381 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101452077 | AGAATTGCTCGAATC[C/T]CAGTAAATTATGATC | 8945 |
rs112870968 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101359479 | GTTGCCCAGACTGGA[A/G]TGCAGTGGCACAATT | 8945 |
rs112908047 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101545632 | AGAAGATGACCATCT[A/G]CAAGTCAAAGGAAGA | 8945 |
rs112908889 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101516767 | GCATGACTCCTTATG[A/G]TTATAGCAATATCTC | 8945 |
rs112951928 | snp | C/T | 0.0667028 | 0.170006 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554705 | TAAACAGCTGGACCT[C/T]AGCAAGGGTCAGGCA | 8945 |
rs112967266 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101437843 | ACCGTTCTGCTTACC[G/T]GAAAAAACCCCTCCA | 8945 |
rs112979099 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101464479 | TGTTTTTTTCATTGC[C/T]GTTTTAGCAGGTTCT | 8945 |
rs112983777 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101381123 | CCTTATTCTTGGGTG[A/G]TGATAATAATAACAA | 8945 |
rs112995510 | in-del | -/ACTTAG | 0.383632 | 0.211288 | intron-variant | BTRC | GRCh38.p7 | 10:101518846 | AAATGATCTCTAACC[-/ACTTAG]CACTTAAATAATCCT | 8945 |
rs112996240 | in-del | -/T | 0.497776 | 0.0332724 | intron-variant | BTRC | GRCh38.p7 | 10:101456544 | TTGATTTTGAGACAG[-/T]TTTAAGCTTATCACC | 8945 |
rs113009977 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101435221 | TTTATTTAGGTAAAA[C/T]TTACATACAGTGAGA | 8945 |
rs113062112 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101415157 | ATGGTTAAGTGCCCT[A/G]TATAGGTGTACCATT | 8945 |
rs113084874 | snp | A/G | 0.383824 | 0.211166 | intron-variant | BTRC | GRCh38.p7 | 10:101509550 | TGAGCCACCGCGCCC[A/G]GCCTTTTTTTTTTTT | 8945 |
rs113090359 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101394557 | CCGCTTCCCTACTCC[A/G]CAAAATACATAGTCA | 8945 |
rs113102659 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101423164 | AGCAGTCCTCCCACC[G/T]TGGCCTCCCAAAGTG | 8945 |
rs113115051 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | BTRC | GRCh38.p7 | 10:101359496 | GCAGTGGCACAATTT[C/T]GGTTCACTGCAACCT | 8945 |
rs113137058 | snp | A/C | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101536736 | TTAAACATAACCATT[A/C]CTTGTTTCTAAAAGC | 8945 |
rs113152873 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101438503 | TTTTTATGTCTCACA[C/T]ATACACATACATATA | 8945 |
rs113156121 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101512454 | GGAATGTCTTTCTCT[A/G]CTTACTATACCCTTC | 8945 |
rs113202450 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101405254 | ATGGGAGGCTAGAGG[A/G]AAAAAAAAAAGCAAT | 8945 |
rs113211577 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101385088 | ACAGAACAAAATTAG[C/T]GTGGCATGGTGGTGC | 8945 |
rs113239655 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101401211 | GTATTTAAGTACAGG[C/T]ATAGGTGATTGAGTT | 8945 |
rs113267152 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101440315 | GGAAGCACTATTGAT[A/G]TATGCTTTCATTTTC | 8945 |
rs113302583 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514497 | AAGCTCTGTCACCCA[A/C]TCTAGAGTGCAGTAG | 8945 |
rs113329862 | snp | A/C | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101516231 | GGTGGTGTGCTAAGC[A/C]TGCTTTTCATGAGGG | 8945 |
rs113337527 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101376645 | TCATCTTCATTTATT[C/T]TAAAGATGCTGTGGC | 8945 |
rs113356035 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101421755 | TGATAGTTTGCTGAG[A/G]ATGATGGTTTCCAGC | 8945 |
rs113362410 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553966 | TGACCCTGTGGCAAC[A/T]GTGGATTCTCAGACA | 8945 |
rs113369211 | in-del | -/ATAG/ATAGATAG | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101436625 | TTTCAATTAAAAAAA[-/ATAG/ATAGATAG]ATAGATAGATAGATA | 8945 |
rs113371036 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101370105 | TATTTCTGTATGGAC[A/C]TATCCCTTATCCTGT | 8945 |
rs113384285 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101439497 | TAAAGTTGCAGTATC[A/G]TTGCACATTCCTTGT | 8945 |
rs113484245 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101551176 | ATGAAAATAAAATGA[G/T]ATTTGAATCAGTTTG | 8945 |
rs113490639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360660 | ATAGGCATTAGCTAC[C/T]GCGTCTGGCCTCTAG | 8945 |
rs113520556 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101401385 | CTGTCAAGGGGAGAA[C/T]AAAGATACCACCTGG | 8945 |
rs113540178 | snp | A/G | 0.208474 | 0.246527 | intron-variant | BTRC | GRCh38.p7 | 10:101455163 | TTAAGCGATCCTCCC[A/G]CCTTAGCCTCCTGAG | 8945 |
rs113554149 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101474180 | TAGTAATTTTTGATC[A/G]TATAACCAACATTAT | 8945 |
rs113559463 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454821 | GAAATTTCAAGATCA[G/T]ATCACCTGTTGGTGA | 8945 |
rs113587011 | in-del | -/A | 0.3748 | 0.216622 | intron-variant | BTRC | GRCh38.p7 | 10:101385207 | GTCTCTAAAAAAAAG[-/A]AAAAAAAAAATTAGC | 8945 |
rs113590309 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101371041 | GTTAAGTAGTGTTAA[A/G]TATATTCACACTGTT | 8945 |
rs113593124 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101368668 | TCATTTTATACTTTC[C/T]TTAGCAGTGTATGGG | 8945 |
rs113650382 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101474071 | TTTAGAGCTATAATA[G/T]GTGCTAATTTCTACA | 8945 |
rs113687421 | snp | G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101465407 | GAGCTATTTAAATAT[G/T]GGAGGAGCAAACAAC | 8945 |
rs113707398 | in-del | -/AG | 0.084364 | 0.187256 | intron-variant | BTRC | GRCh38.p7 | 10:101527358 | TATACCAAATGCCTC[-/AG]AGATTTTTATCATTC | 8945 |
rs113720000 | snp | G/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101491250 | TTCAGGGTGGTGACT[G/T]ACTTTAGTAATTGTT | 8945 |
rs113721801 | snp | A/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101542290 | TGATTTTTTTTTTTT[A/T]TTTTTCTAGCTTCTT | 8945 |
rs113746548 | snp | C/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101390354 | TTTTTTTTTTTTTTT[C/T]CGAGACGGAGTCTCG | 8945 |
rs113763313 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101440791 | GAAAGGCAAGAGCTG[-/T]TTCTGCATCAGTCTA | 8945 |
rs113821473 | snp | A/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101401907 | CAGGGCAAAAAAAGA[A/T]GGAAAAAAGAAAAAC | 8945 |
rs113865475 | in-del | -/GCTT | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101532809 | TGTGCGCGCGCGCGC[-/GCTT]GCTTAGCTATACCTA | 8945 |
rs113873809 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101526537 | GCAATCCCAGCACTT[C/T]CGGAGGCCAAGGTGG | 8945 |
rs113879352 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101367172 | GCCTCCCAGGTTCAA[A/G]CCATTCTCCTACCTC | 8945 |
rs113918433 | in-del | -/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101523936 | GTAGGAATCCTAGGG[-/G]AAAAAATACAGACAT | 8945 |
rs113935163 | snp | C/G/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101539177 | GTTCCCCATATACCC[C/G/T]CTTTTGACATTTGGG | 8945 |
rs113936412 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101536073 | CACAAAAGTTCTTGA[G/T]AACTGACTTTGCATT | 8945 |
rs113939986 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101420062 | GGTATATGTGTACAT[A/G]TATATATATATATCA | 8945 |
rs113950695 | snp | C/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101527761 | CCTGTCTCTTTCTCT[C/G]TCTCTCTCTCTCTCT | 8945 |
rs113978184 | snp | A/G | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101369006 | CTTTGGCGACAGAGC[A/G]AGACTCCATCTTAAA | 8945 |
rs113992493 | snp | A/C | 0.383439 | 0.21141 | intron-variant | BTRC | GRCh38.p7 | 10:101509401 | CTGGGACTACAGGCG[A/C]CCGCCACTACGCCCG | 8945 |
rs114090045 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | BTRC | GRCh38.p7 | 10:101419430 | TGAGGTCTCATTTGA[A/G]GGTTTTATTTCGAGA | 8945 |
rs114138983 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101469495 | TGAAGGGAAAAGAGG[A/G]TAATTTTGAAGGAAA | 8945 |
rs114320522 | snp | A/G | 0.208474 | 0.246527 | intron-variant | BTRC | GRCh38.p7 | 10:101499280 | GAGTCTCGTTCTGTC[A/G]GGCTGGAGTGCAGTG | 8945 |
rs114453878 | snp | A/C | 0.0333238 | 0.124705 | intron-variant | BTRC | GRCh38.p7 | 10:101381295 | CACAGACAGGTTGTT[A/C]CTTTTTCCAGATCAA | 8945 |
rs114616649 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | BTRC | GRCh38.p7 | 10:101357696 | TCTCACAAATTTGCT[C/T]ATTGCTATACTAAAG | 8945 |
rs114616991 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101502962 | ACTTATGCCCTTACT[A/G]TGTGCCAGGTACTCT | 8945 |
rs114699620 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101453970 | TGGATGGGCATGGCT[A/G]TGGGCCAGTTAAACT | 8945 |
rs114703440 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | BTRC | GRCh38.p7 | 10:101499283 | TCTCGTTCTGTCGGG[C/G]TGGAGTGCAGTGGTG | 8945 |
rs114766338 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101450274 | ATAACTGTTTTAGCC[C/T]CCTCCCTTTTTTGGT | 8945 |
rs114766664 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101544851 | TTGCTTGAACTCAGG[A/G]GTTCAAGACCAGCCT | 8945 |
rs114782347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101368834 | GTCTAGCCTGGCTAA[C/T]GTGGTGAAACCTCGC | 8945 |
rs114943798 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | BTRC | GRCh38.p7 | 10:101435104 | GTATCTTCTCTGCCC[A/G]CCTACTGGAATTACA | 8945 |
rs114952530 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101428418 | TGTTTATAAAATGGA[A/T]CGTAGCTTGAGGTGA | 8945 |
rs115079283 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514774 | TTGAATTATCTTGGC[A/G]TCTTTCTTGAAAGTC | 8945 |
rs115112317 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | BTRC | GRCh38.p7 | 10:101375194 | ATGGGGGCGGATTTC[C/T]GCCTTTTGTGCTGTT | 8945 |
rs115226572 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | BTRC | GRCh38.p7 | 10:101485201 | AGAGACTTAAAAAAA[A/G]AAGTCCAGACCCCAG | 8945 |
rs115250463 | snp | C/T | 0.021333 | 0.101051 | intron-variant | BTRC | GRCh38.p7 | 10:101408769 | AATATTGAGGTTGGC[C/T]GGGCACAGTGGCCCA | 8945 |
rs115285153 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101445778 | CAGAATTCCCCAGAG[A/G]CCTTGGACTCTCTTA | 8945 |
rs115293909 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101424515 | CAGTACAGCAATCTT[G/T]TTATTGTTGATTATT | 8945 |
rs115351147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101465792 | TATACCTGCTTTTTC[A/G]TTTCATTTCCAGCAT | 8945 |
rs115628195 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | BTRC | GRCh38.p7 | 10:101485363 | AAACTTTGCCCTGAG[G/T]GGGCATCAGACTGGC | 8945 |
rs115639456 | snp | A/T | 0.031825 | 0.122064 | intron-variant | BTRC | GRCh38.p7 | 10:101459150 | CTTATATTAATCACT[A/T]ATCCTTAAATAGAAT | 8945 |
rs115852956 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101504365 | AGCTTGGTAATGCTG[A/G]GTCCCTTTTGCATTT | 8945 |
rs115920981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101442566 | ATTAAGATATATTTT[A/G]TTAGGCATAAAGTTT | 8945 |
rs115952020 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101400097 | GGGGAGGGTAGATAA[C/T]GTTCATTTTTGTTAC | 8945 |
rs115953200 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101490570 | CCTTTCAGGTAGTAT[G/T]TGGAGGCCTCTGCAC | 8945 |
rs115965795 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101458203 | GGAAAAGAAATACTA[C/G]TATTTACAACAACAT | 8945 |
rs116021911 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | BTRC | GRCh38.p7 | 10:101451551 | CTGTGTTAGCTGTAG[G/T]TGTTAAAGCAGTAGT | 8945 |
rs116023388 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | BTRC | GRCh38.p7 | 10:101373232 | ATTTGAATCTGATTC[C/T]CACTGGGAGCAATAA | 8945 |
rs116028301 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101366689 | AGTGAGTTATAGGTG[A/G]GTAGATAGATATAAT | 8945 |
rs116030893 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | BTRC | GRCh38.p7 | 10:101427671 | GTAGCTAGGACCACA[A/G]GCATGTGCCACCATG | 8945 |
rs116039155 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101449968 | TGTAGTTTTGTAATT[G/T]CATTCGTACATTAAG | 8945 |
rs116056215 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500200 | AATCTAAATGGTACA[A/G]CCTCCTATACACCTA | 8945 |
rs116152716 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101485417 | CGCATTGATTAGGCA[C/T]GTTGGCCATCAGCAT | 8945 |
rs116177665 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | BTRC | GRCh38.p7 | 10:101464374 | CACATGGGACTAATC[G/T]GATTCATTTTAAAAA | 8945 |
rs116279069 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101436682 | TAGATTTATATGGCC[C/T]TAGAATACTTTAGCT | 8945 |
rs116296053 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | BTRC | GRCh38.p7 | 10:101533822 | GTTCCTGTTTTTTGT[C/T]TTTTGACTTAAAGGC | 8945 |
rs116297442 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | BTRC | GRCh38.p7 | 10:101550256 | CTTTAGCCAAAGTAA[A/G]TTTTCTCTATTTTTT | 8945 |
rs116445780 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101532561 | TAGATTGTTTCCAGT[C/T]CCAAAGCCAAAATCA | 8945 |
rs116488041 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | BTRC | GRCh38.p7 | 10:101421158 | AATTCATTTTTCCTT[A/G]TGATCAGTTATCCAG | 8945 |
rs116496968 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101413814 | TTAATTTCAACTTTC[A/G]TGTTTTTTTATATAC | 8945 |
rs116534522 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101358680 | CTTCACTTCTCCTCT[A/G]TATGGGCCTTTCTCT | 8945 |
rs116572772 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101475214 | TTATAAGAATAAAAC[A/G]AGTTGGTAAATTTTT | 8945 |
rs116608882 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101452421 | ATTGGAATTCTCCTA[C/T]CCAAGGCTTCCATTA | 8945 |
rs116643568 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | BTRC | GRCh38.p7 | 10:101484063 | AGATTCCTGGCCCAG[A/G]TAAGAGAAGTTTTTC | 8945 |
rs116643748 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101402770 | CACAACCTGATATGT[C/T]ATGCCTTCTCAGTTG | 8945 |
rs116738217 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101485766 | GGGAGCTAATAGGCT[C/T]GAGCTTGTCTTTGTG | 8945 |
rs116755494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101447334 | TGGCATTTAGAAATG[A/G]CCATGTTTTCTTTAC | 8945 |
rs116791178 | snp | A/G | 0.031825 | 0.122064 | intron-variant | BTRC | GRCh38.p7 | 10:101380703 | GTGATTGAAACCACT[A/G]TTGGCATAGTGGAAA | 8945 |
rs116869248 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101504579 | CTTTCCCCAATCCTC[A/G]GTCACTTTTGTCATT | 8945 |
rs116915140 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101365801 | TTCTTTTATGTTTTA[C/T]GGATTTTCTACAGTG | 8945 |
rs116952915 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101506039 | CCTGCCTCAGCCTCC[C/T]ATTAGCTGGGACTAC | 8945 |
rs116954743 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101426851 | GGTGGCTTTAGTATG[A/G]TTAAAAGTGTCGCCT | 8945 |
rs116990303 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101435258 | GATCATAAGTGTACT[C/G]TTAGGTGAGTTTTGA | 8945 |
rs117021611 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101412114 | TGCTGAGCTTATAGT[A/T]CTGTTGTAGTTTTTT | 8945 |
rs117057068 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101475264 | AAGAAAAACAGCTGG[A/G]CGTGGTGGCTCACGC | 8945 |
rs117058643 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | BTRC | GRCh38.p7 | 10:101375765 | GGAATGCATGTTAAA[A/G]TGTAGTACAGATTCT | 8945 |
rs117120739 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BTRC | GRCh38.p7 | 10:101445394 | TCAGTATCTATAAAA[C/T]ATATTTCAACTGCTG | 8945 |
rs117159636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101446844 | ATGTTTCTTCCCTCT[A/G]TCCCCCAAAGATCTA | 8945 |
rs117162006 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101458229 | AACATGAGTAGATCT[C/G]AGATATTTTATGCTA | 8945 |
rs117189620 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | BTRC | GRCh38.p7 | 10:101394592 | CTGACTAGTAATGAG[C/T]AAAACAAAAGCAAAC | 8945 |
rs117217752 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101458608 | CAGTGTGTGCTATAC[C/T]TCTTTAGTTTCCTTT | 8945 |
rs117300042 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | BTRC | GRCh38.p7 | 10:101440954 | CTCAGAAAGTAATAC[A/C]AAAAGGAGGGATATT | 8945 |
rs117326913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101507442 | AGGCTCTGTGCCGCT[C/T]CGATCCGGGGAAATG | 8945 |
rs117342345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101461222 | GCAGGGTTTTAAATA[C/T]TAATGTTATTAATGT | 8945 |
rs117352093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101466070 | CATGAAAGTACTCAT[C/T]ACTTTTTGAAAATTG | 8945 |
rs117373316 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101531962 | AGCAATCAGTAGCAA[C/T]GGCCATCACATATGT | 8945 |
rs117425258 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | BTRC | GRCh38.p7 | 10:101395926 | GTTTGTAAGCGACAA[A/G]TATGTATATATATAT | 8945 |
rs117452441 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | BTRC | GRCh38.p7 | 10:101447012 | GTGGTGGGGGGGCCG[A/G]TTACAAAGCAATAGA | 8945 |
rs117458764 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353528 | GTGTGGGTGGCGATG[A/G]CTTAGGAGGACCTTG | 8945 |
rs117550974 | snp | A/G | 0.0678174 | 0.1712 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406888 | AAGCTTTTTACTTTT[A/G]ATTTATTGGTATACA | 8945 |
rs117612167 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101424625 | ATGCTGAGGCTAGCC[C/G]TTTGCCTGCAGGGCT | 8945 |
rs117615009 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | BTRC | GRCh38.p7 | 10:101424411 | TGTATTACATGATTA[C/T]GGTATACTGCATTTC | 8945 |
rs117631105 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101418914 | CATGTTGTTTTCATA[C/T]ACATATTCATTGTAA | 8945 |
rs117680889 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101401270 | GTTTTACTCTTATCA[C/T]GTGAATGAGCATTCA | 8945 |
rs117728343 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | BTRC | GRCh38.p7 | 10:101408545 | CTCATGGACGCAAGC[G/T]ATCTGCCACCTGGGC | 8945 |
rs117750527 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | BTRC | GRCh38.p7 | 10:101432826 | ATGGAGTCATGGATG[A/G]CATTACTGCCTCCCA | 8945 |
rs117800392 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383397 | ATAAGTCTTCCTTTT[A/T]AAAAAAAAAAAAAAA | 8945 |
rs117842157 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101530663 | TGATATTATAATATT[C/T]CTAAAGGCTTGGTAC | 8945 |
rs117860945 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407314 | GATCATACCACTGCA[A/C]TCCATCCTGGTTGAC | 8945 |
rs117865804 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101504288 | CTCCTCTCCCTCTTG[A/T]TGTTTATTGTGTGGG | 8945 |
rs117876115 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385385 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAAAGTG | 8945 |
rs117898309 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101500233 | CTATATGGTATACCT[A/G]TTACTCCTAGGCAAC | 8945 |
rs117901631 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101418046 | TATTACATAACAAAT[C/T]ACCTCAAATTGAGTG | 8945 |
rs117910449 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101432989 | TGGTGTTGAAACTTA[C/T]AGGTATGGTTTAGTG | 8945 |
rs117923713 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | BTRC | GRCh38.p7 | 10:101519966 | CGCTATTGCACTCCA[C/G]TGTGGGCAACAAGAC | 8945 |
rs117932321 | snp | A/G | 0.077417 | 0.180873 | intron-variant | BTRC | GRCh38.p7 | 10:101389774 | AGACCACAGGTGCAC[A/G]CCACCATGCCTGGCT | 8945 |
rs117969640 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | BTRC | GRCh38.p7 | 10:101539176 | TGTTCCCCATATACC[C/G]CCTTTTGACATTTGG | 8945 |
rs117991265 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518852 | ATCTCTAACCACTTA[A/G]ATAATCCTATTAGTT | 8945 |
rs117998275 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101424134 | AGCTACTCAGGAGGC[G/T]TAGTCAGGAAAATCA | 8945 |
rs118046259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381692 | TTATGAGAAACACAC[A/G]ATGATAACTCATATA | 8945 |
rs118051685 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101377203 | AATGCCTTTGAGCTA[A/G]ATTAATCCATGTTTT | 8945 |
rs118053433 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101467962 | ACAAAAGTGATCTTT[C/T]CAAATCTGACGAAGT | 8945 |
rs118137938 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101528122 | CTCCTGAAATTTCAG[A/T]TAAGGAGATTCATTC | 8945 |
rs137897352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355525 | TACAACTAAAGAATG[A/C]TGGAATGCATAGATT | 8945 |
rs137912587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101495959 | CACTTCTAACACCAT[A/G]CATTAGTTCTGCCTG | 8945 |
rs137931953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394797 | AGGGCAAGAATAGCA[A/G]TTTGACCAGTGAGTT | 8945 |
rs137967560 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101545330 | AGAAGGCTAAACTTA[C/T]GTTGTCTACAAGAAA | 8945 |
rs137979978 | in-del | -/TTTTTGTTTTTTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101363456 | TCGTTTTTGTTTTTG[-/TTTTTGTTTTTTC]TTTTTTTTGAGATGG | 8945 |
rs138007808 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555383 | GTTTCTAAGACTGTT[C/T]TGAGACATGTCCAGT | 8945 |
rs138008006 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101384897 | TGAATTTTTAATTGC[A/T]TAATTGAAACTATGG | 8945 |
rs138033555 | snp | A/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406929 | ATTGTGTCGGTTTTT[A/T]AATTAATCATCTGTC | 8945 |
rs138043387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488102 | AATCAGGTAACCAGA[A/G]GAATTACATTTTTTA | 8945 |
rs138048012 | snp | A/T | 0.040671 | 0.13668 | intron-variant | BTRC | GRCh38.p7 | 10:101387836 | CTGGGATTACAGGTG[A/T]GTGCCACCATGCCCA | 8945 |
rs138062361 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101427704 | CAGCTATTTTTTAAA[C/T]TTTTTGTAGAGATGG | 8945 |
rs138099881 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101518855 | TCTAACCACTTAAAT[A/T]ATCCTATTAGTTTTT | 8945 |
rs138113862 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101531675 | GCAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 8945 |
rs138114439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471992 | TCTTCATCGTTCTGA[A/G]TATTTCCATCTTATA | 8945 |
rs138181232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101420614 | ATTAGGGCTCTGTCA[C/T]CTCATGCTGGGTCCC | 8945 |
rs138188016 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101518443 | TAAGCAGAAGTTGCC[G/T]GGGCTTAGAAGTCCC | 8945 |
rs138224461 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101523681 | CCTGTTTTCTCTACG[C/T]ATGTGTATTTGCCTA | 8945 |
rs138261389 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101511169 | TCTTAGCCCCAGCCA[C/G]CTTAATTCCCACCAT | 8945 |
rs138264330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408544 | ACTCATGGACGCAAG[C/T]GATCTGCCACCTGGG | 8945 |
rs138266519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101371923 | TGAGGCTGAAAACCC[A/G]ATCGTCATGCTTACA | 8945 |
rs138269319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101367859 | TTGATGGACACTTGG[A/G]TTATTTCCAGTTTTG | 8945 |
rs138270273 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | BTRC | GRCh38.p7 | 10:101477909 | CCCACCTCGGCTTCC[C/T]AAAGTGTTAGGATTA | 8945 |
rs138285266 | in-del | -/TTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101427132 | TTTTTTTTTTTTTTT[-/TTTTT]GAGACGGAGTCTTGT | 8945 |
rs138285433 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101356503 | TTGAGTTAAAGTGGA[C/T]TTGGAGATGACCATA | 8945 |
rs138324123 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101383701 | TGCTTTCTTTAATAG[A/C]TATGAGAATAATATG | 8945 |
rs138368900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101504052 | TTTCTGATGCTAACT[A/G]AAGGGAGAAGGGTGT | 8945 |
rs138381840 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101365186 | TCAAGTGATTCTCCT[A/G]CCTTAGCTTCCTGAG | 8945 |
rs138403335 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101467947 | GGTCTCTTAAGTAAG[A/G]CAAAAGTGATCTTTC | 8945 |
rs138474192 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | BTRC | GRCh38.p7 | 10:101532781 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGCGCGTG | 8945 |
rs138488639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101449368 | CCTAAGGGTTCTATA[A/G]TTCTCAGTCCTATTT | 8945 |
rs138493548 | in-del | -/AC/ACAC | | | intron-variant | BTRC | GRCh38.p7 | 10:101527795 | CTCTCTCTCTCACAT[-/AC/ACAC]ACACACACACACACA | 8945 |
rs138509858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101547450 | GGTGCAAGCTATTCT[C/T]CTGTCACAGCCTCCT | 8945 |
rs138528205 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556736 | GCCTGGTTTCAGGTG[A/G]AACTTAATGCATTGA | 8945 |
rs138531213 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101546963 | ATATCAATTTTCTGT[-/TA]TCTCTTCTATAAGAT | 8945 |
rs138589941 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544131 | AGCCAAGATGGTCTC[A/G]ATCTCCTGACCTCGT | 8945 |
rs138603635 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | BTRC | GRCh38.p7 | 10:101436487 | CTGTCTCTACAAAAA[A/T]TTAGCTGGGTGTGGT | 8945 |
rs138626807 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101488718 | TGTAAATGAATTCAA[A/G]TATCTTCTAAAGATA | 8945 |
rs138659432 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101495409 | TAATTATTCATATCA[C/T]AGCAACAATTAAAGC | 8945 |
rs138661751 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101393891 | CTCTCCAGATTTCAT[A/G]TATTGTGGAAAAGCA | 8945 |
rs138671088 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101524038 | AAAAATATACCAGCT[C/T]ATAGCCTCCCAACTA | 8945 |
rs138731809 | in-del | -/TA | 0.0869089 | 0.189476 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406035 | GTTAGGCTCTCAAAC[-/TA]TGTAGATTTGTGTAT | 8945 |
rs138758817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101476246 | GGGATTGTTGAAAAT[A/G]AGAGGAGCCCTAAGA | 8945 |
rs138837616 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101478588 | TTGAGCTCAGGAGTT[C/G]AAGACCAGTTTAGGC | 8945 |
rs138879096 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101455133 | ATGGCATGATTACAC[C/G]CCAAACTCCTGGGCT | 8945 |
rs138902161 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101517669 | TCCTTTAAAGAAATA[C/T]TTTCTTCAGAGTAGC | 8945 |
rs138959296 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101363303 | TGAGAGCCTTACTTA[C/G/T]GTGCAGTATACTTCC | 8945 |
rs138959622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101416946 | TATTTTTATTAATTT[A/G]TATTCCATGTTTTAT | 8945 |
rs138970392 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101378681 | AGGAATGAGCCACCA[C/T]GCCCGGCTAATTTTT | 8945 |
rs138976519 | snp | C/T | 0.122411 | 0.214991 | intron-variant | BTRC | GRCh38.p7 | 10:101483533 | GGGAGGCAGAGGTTG[C/T]AGTAAGCTGAGATCG | 8945 |
rs138978402 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101417567 | GGTTTTTTTCCCACT[A/G]TAGAATTAACTTTAT | 8945 |
rs139018865 | in-del | -/TGTGTGTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101442297 | CTGTCTCTGTGTGTA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 8945 |
rs139034306 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101367161 | CTGCATCGTCTGCCT[C/T]CCAGGTTCAAGCCAT | 8945 |
rs139044855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539937 | GCCATCTGTATATCT[C/T]CTTTGGTGAAGTGTG | 8945 |
rs139057748 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101426366 | TATAGTTTTCATACC[C/T]ATACCAATTGTCTTG | 8945 |
rs139073014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424502 | ATACGTAAACTCTCA[C/G]TACAGCAATCTTTTT | 8945 |
rs139102832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101430471 | CTTTCTCTGTCTCTG[C/T]GGGTTATTTGCGGGC | 8945 |
rs139115116 | snp | A/G | 1.65597e-05 | 0.00287743 | intron-variant | BTRC | GRCh38.p7 | 10:101479474 | TAAGTAATATTGCTC[A/G]TCAATGTATATTACA | 8945 |
rs139134033 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101458952 | CAAACTTTCACTCAC[G/T]TATTGTAGTTTTAAA | 8945 |
rs139163007 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101456499 | TAGAAATGAGTGGAG[-/A]ATGGTAAAAGAGTGC | 8945 |
rs139245829 | snp | A/C | 0.000230969 | 0.0107439 | intron-variant | BTRC | GRCh38.p7 | 10:101414711 | TATTGATGATCCTTG[A/C]TCTCTGTGGGCCTAG | 8945 |
rs139248641 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101380565 | CCCAGACAGGGCAGC[A/G]GCTATTAAGAACCTC | 8945 |
rs139256148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498974 | CTCCAGCCTGGGCAA[C/T]AAGAGCGAGACTCTG | 8945 |
rs139359490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101490777 | TTACTATCTCTTTTC[A/G]GCTGGGTGTGGTGCC | 8945 |
rs139401213 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101510082 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCATTG | 8945 |
rs139406401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506521 | GGAGGACAGGCATTG[A/G]TGAGCAGCAGTTCTA | 8945 |
rs139444868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514323 | TTTTCTCCTGTGTTT[C/T]CTTTTAGAAGTTTTA | 8945 |
rs139484685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101451589 | AAGAATGTGTGCTGT[A/G]CAAATTCTGGCTTGT | 8945 |
rs139525100 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101455536 | AACTGCAGGTTAGGC[A/G/T]TAAGGGGATAAAGGC | 8945 |
rs139539798 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101363913 | TCATTTCAGTTAGCT[A/G]TTGGCGTTTAGAATC | 8945 |
rs139542697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101423937 | TTTGCAGCTTTTAGA[A/G]TCCTTATTTTAGCCG | 8945 |
rs139550918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515371 | TATTGCACTAACTCT[A/G]TAGGTTGATTTGGAA | 8945 |
rs139561760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375817 | CCCTTTTACTTGGTA[C/T]GCCTAAAAAATTGGC | 8945 |
rs139637547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525185 | CTTCTGAGACCTCAG[G/T]ACAGATTTGGGTGGT | 8945 |
rs139639795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417626 | TTGTGGGGAGGTATT[C/T]TGAGACTATTTAAGT | 8945 |
rs139678043 | snp | C/G/T | 0.00239401 | 0.0345304 | intron-variant | BTRC | GRCh38.p7 | 10:101369566 | ATTTCTCTGAGAAGC[C/G/T]CTTTTAGAAGTTTCT | 8945 |
rs139681293 | snp | A/G | 0.000148988 | 0.00862971 | intron-variant | BTRC | GRCh38.p7 | 10:101461946 | ATAAGATTGAAGATA[A/G]TGAGAACTGAATTAA | 8945 |
rs139682728 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101368285 | TCGCCCTCCACCGTG[A/C/T]GTGGAAGCCGCTTGA | 8945 |
rs139692442 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101446934 | TAGGGAGAAGGATAC[A/G]AGATTGATTTTTTTA | 8945 |
rs139721697 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496015 | TATTTTTTTTTTTTT[-/T]ACTGTCTGAATTATT | 8945 |
rs139798948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101480481 | TGGTGAGGGCTTGCT[C/G]TCTGCCTCATAGATG | 8945 |
rs139801100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101381208 | ACTATATATATTAAC[C/T]CATTTGATCCTCTCA | 8945 |
rs139818083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391644 | AAAATAAATTTGGGA[A/G]ATTTGCTCTCTAGAA | 8945 |
rs139818342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484757 | AAACTGTGGAGTATA[A/C]TGTGTTACACATTGG | 8945 |
rs140004702 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532783 | GTGTGTGTGTGTGTG[C/T]GTGTGTGCGCGTGTG | 8945 |
rs140014243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404285 | TCCGCCCTCCTCGGC[C/T]TCCCAAAGTGCTGGG | 8945 |
rs140022721 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101441606 | TTTTCTTGGCCGGGC[A/G]TGGTGGCTCATGCCT | 8945 |
rs140024589 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | BTRC | GRCh38.p7 | 10:101512891 | GCAGGGGTGGCAGAA[A/C]TTTAGTGTTACCATT | 8945 |
rs140033838 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101409888 | CATGTGTATACATGT[A/G]TTTGTTTACCTGTTT | 8945 |
rs140039858 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101385903 | TATTTTAATATAACT[A/G]AGTTGTGACCTGTTT | 8945 |
rs140056778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101466789 | CTGGGCCTTATAAAA[A/G]GAACTACATAAGTCT | 8945 |
rs140063679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101386593 | AGTTTTTATGAGATA[C/T]CGATAAAAAGTATTG | 8945 |
rs140063814 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101445822 | TGTTGTGTACCCTGA[A/G]GATGAAGTGCAGTTT | 8945 |
rs140070073 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | BTRC | GRCh38.p7 | 10:101370834 | GCCTCTGCCTCCCCA[A/G]GTGCTGGGATGCTGG | 8945 |
rs140076652 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532777 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGCG | 8945 |
rs140099180 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101390933 | CTTGTAGGGAATTCA[C/T]TTATGTATTTTGAAA | 8945 |
rs140141029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395233 | GTTGGAGAGAGATGG[A/G]GTTTTGTATATTATT | 8945 |
rs140195021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448705 | GAAAATGGAAAGCAG[A/G]ATTTACAGCAGAAGT | 8945 |
rs140203839 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101485222 | CAGACCCCAGCCCAG[A/G]ATCTTTATGAATTAT | 8945 |
rs140231696 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101429504 | CTCTTCCTCTCCCCT[-/C]CCCCCCCTCCCCTCC | 8945 |
rs140307285 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101405431 | AAGAAAAATGGGAGA[C/T]TTTTGCCATTCTCTC | 8945 |
rs140318589 | snp | C/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101501790 | TTCAAAGAAAGGATA[C/G/T]AAGTCCTAATTTTAA | 8945 |
rs140334571 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101503343 | GAGCTTCATTGTCAT[-/T]GAAAAGAGGAAGAGG | 8945 |
rs140399004 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101444112 | ACTTATGTTCATATC[A/C]GATATATCTCATCTC | 8945 |
rs140408441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487334 | AACTATATGAAGAAC[A/G]GGATTTTTCAGAATA | 8945 |
rs140438501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447777 | ATTCATTAAAATTAG[C/G]CTAATTTGAATTTCA | 8945 |
rs140473979 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101473892 | CATGAGCCACCATGC[A/G]CAGCCTGAATTTTTC | 8945 |
rs140474195 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101411377 | TGCATTTTCCAAATA[C/T]ATTTTCTGCTTCTGC | 8945 |
rs140511455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101482173 | TACAGAAGTGTGTCA[C/T]CACACCCAGCTAATT | 8945 |
rs140532186 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101419956 | TGGTTCCTTTTAGTG[G/T]AGAGTGATATTTTGA | 8945 |
rs140622262 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101523121 | GGGCAGGAGAATCGC[C/T]TGAACCCAGGAGGCA | 8945 |
rs140642584 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101528451 | CCAGGATCCAGCACT[A/C]ATTACCACTTTTTTC | 8945 |
rs140665295 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101371273 | GGCTCACTGCAGACT[A/C]CGCCAAGCAATTCTC | 8945 |
rs140673720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521114 | CTCTACAAAAAAAAA[C/T]GTTAAAAATTAGCAG | 8945 |
rs140712259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402551 | CCTTTAGTCCAAGTT[C/T]CGTGGAGAAAATAAT | 8945 |
rs140735919 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101474770 | TCAGGGGAAAAGCAC[A/G]TAAACACACATCTCA | 8945 |
rs140740002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377123 | ATTTTATGTTTTTGA[G/T]AATGTCATATAAATG | 8945 |
rs140771493 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101503536 | AACAATTACCAAAGT[A/G]TTCCAGAGAGAAATG | 8945 |
rs140780373 | snp | A/G | 0.000963757 | 0.0219306 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532297 | TCCTTCTTCTCAGAC[A/G]ATAGAATCTAATTGG | 8945 |
rs140831102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451954 | TGATAATGTCAATCT[A/G]GCAAAATATATACAC | 8945 |
rs140836879 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | BTRC | GRCh38.p7 | 10:101491638 | GGAGGCGGAGGTTGC[A/T]GTGAGCCAAGATCGC | 8945 |
rs140853032 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101491781 | GATTCATGCTTCTAG[A/G]TGGTTCGGTGATTGT | 8945 |
rs140882442 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | BTRC | GRCh38.p7 | 10:101494491 | TCATAACTCAAAAAA[A/T]ATTTTCTTAATTTTG | 8945 |
rs140903083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436070 | AAGTTGTTAGAATAA[A/G]TTCTATGGGGATATG | 8945 |
rs140919649 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555717 | TGACCTTTTTAAAAC[A/G]AAAAGAGAGACAAAG | 8945 |
rs140932704 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101440795 | GCAAGAGCTGTTCTG[C/T]ATCAGTCTAGTGAAA | 8945 |
rs140933844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101444932 | ATTAGTGGTTTTCTC[A/G]TATATAGTAGGGCAT | 8945 |
rs140971602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448487 | AAAAATTGAAGACAT[A/G]AATTGGTGTGTATAA | 8945 |
rs140993326 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521826 | GGCACATAAACTCGT[A/G]TCTTAAACCTATGTT | 8945 |
rs141008374 | snp | A/G | 0.00412634 | 0.0452343 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534803 | GATATGGCCTCCCCA[A/G]CTGACATTACCCTCC | 8945 |
rs141008546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426094 | CTTTCCACTTTGTTC[C/T]TCATTGCCCAAATTT | 8945 |
rs141017519 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101517583 | TGCCACATTTGGGTT[C/G]CCTTAAGTAAATATG | 8945 |
rs141027093 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101377392 | TGTGAACATTTTCAT[G/T]TCTCTAAATACCCAT | 8945 |
rs141030727 | snp | A/C/G/T | 0.000296584 | 0.0121745 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550823 | AAGCTGAACCCCCCC[A/C/G/T]TTCCCCTTCTCGAAC | 8945 |
rs141086458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406704 | ACAGCTAGCTAATTT[G/T]TGTGTTTTTAATATA | 8945 |
rs141112233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527327 | AACACATAATAAATA[C/T]AATGACCTATAAATA | 8945 |
rs141125856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411699 | TAATTTTTAGGTCTG[C/T]TAATTTCATTGTCAG | 8945 |
rs141127773 | in-del | -/AATT | | | intron-variant | BTRC | GRCh38.p7 | 10:101541945 | ATGTTGGCCTTATAA[-/AATT]AATTTTGAAGTGTTC | 8945 |
rs141216232 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101539028 | CACTCCAGCCTGGGC[A/C]ACAAGAGCGAAACTC | 8945 |
rs141223378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394013 | ATAATTGAGTCTGTA[C/T]CTAGGACTTCCAGGG | 8945 |
rs141227605 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101516151 | AAAGAGAGGGAAGGC[C/T]CAGCTCCAACAGTGT | 8945 |
rs141240135 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101379570 | TGCATAATATACTAC[A/G]TATTTTTTTTTCCTA | 8945 |
rs141257393 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101364818 | ATATTTCTTTTAATT[-/C]TTTTTTTTTTTTTTT | 8945 |
rs141269140 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101360436 | TGGAGTGCAATGGCA[C/G]GATCTCAACTCACTG | 8945 |
rs141292415 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101491059 | GCAAGACTCTGTCTC[-/AA]AAAAAAAAAAAAACT | 8945 |
rs141312784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101468474 | GCCCTAAAAACAACA[C/T]GGAATGATAGCAGAT | 8945 |
rs141332429 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475607 | TTATATATCTCTACT[A/G]TTTTCCCCATTTTTT | 8945 |
rs141353449 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101416572 | TTGTTATTGTTGTTG[C/T]TGTTTTTTACCAGGG | 8945 |
rs141483391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101484778 | TACACATTGGGCTTA[C/T]TGCTCTTTCAAAAAG | 8945 |
rs141492100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535766 | AGATTTGTTTCCTTA[C/G]TAGAAATTATGTAAT | 8945 |
rs141493730 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535388 | GTGAATTTGTAAGGA[C/T]CTTAAATGGACACAA | 8945 |
rs141498287 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101492151 | GAATGAACATAAATT[-/TA]TGTTTTATACCTCAA | 8945 |
rs141499751 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460840 | TGAACCTACAAATAA[A/T]CTAACCCTCCTGTTA | 8945 |
rs141510284 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101427063 | CTACCCAGCACACAC[A/G]GAAACTTAACCAATT | 8945 |
rs141549477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101434726 | TTAAGCCCAGGAGTT[C/G]AGGGCTATAGTGCCT | 8945 |
rs141572799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407413 | ACACCGTAATTTTTT[A/T]TTTTTGTTTTTATTT | 8945 |
rs141582880 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101490469 | AGCTTAGATAAGTTA[A/G]ACCTTTTCCAAATTT | 8945 |
rs141592950 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101390136 | TTTGTGTTTTACTCT[C/T]GAGTATATCCCAGTG | 8945 |
rs141628546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101489065 | ACTTCCCCCTAGTAC[C/T]ATCTCCCTACCCTCT | 8945 |
rs141646345 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101542103 | CTTTAATAAATACAG[A/C]ACTCTTCAGATTTAA | 8945 |
rs141653620 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | BTRC | GRCh38.p7 | 10:101425764 | GCAGTGAGCTGTGAT[C/T]GTGCCACTGCACTCC | 8945 |
rs141692181 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383463 | CCTGCACTTGCCATT[C/T]GAGCAGATATTTTGC | 8945 |
rs141693919 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101484444 | GAACAGTGCAACTGT[G/T]TCACTTTTTTTCCAT | 8945 |
rs141714617 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | BTRC | GRCh38.p7 | 10:101422959 | CAATGCGGGCTCTTT[A/T]TTGGTTCCATATGAA | 8945 |
rs141817613 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101417420 | CTCATGATTAGATCC[A/G]AATTAGGTATCTTCG | 8945 |
rs141822696 | in-del | -/TG/TGTGTGTGTGTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101442296 | CTGTCTCTGTGTGTA[-/TG/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 8945 |
rs141890106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516782 | ATTATAGCAATATCT[C/T]GTTTATTTAATGTAT | 8945 |
rs141890664 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101368007 | ATGTTTAGCTTTATG[C/T]TATGGTTTGAATATA | 8945 |
rs141915205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410058 | GGTTCCAGTTTCTCC[A/G]CATCCTTGTCAGCAC | 8945 |
rs141927527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453283 | GGTTGTCATTCTATA[C/T]GATGATGAGCAGATG | 8945 |
rs141965567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459799 | ATCTGATAAAATAGA[A/G]GGTCAGTAAAAAGAA | 8945 |
rs141991460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101513014 | CAACCAGTAACCATT[A/G]TATCTCTCATACACT | 8945 |
rs141993153 | in-del | -/T | 0.414576 | 0.188188 | intron-variant | BTRC | GRCh38.p7 | 10:101432135 | ATATCTTTTTTTTCC[-/T]TTTTTTTTTTTTGAG | 8945 |
rs142003106 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | BTRC | GRCh38.p7 | 10:101454731 | AGGTTACAAGGAGCT[A/G]TGATCATGTCATTAC | 8945 |
rs142013035 | in-del | -/AG/CA | | | intron-variant | BTRC | GRCh38.p7 | 10:101400419 | AATACTGCTGAGTAT[-/AG/CA]CGGGATCCTTTCATG | 8945 |
rs142019282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548336 | AGCCCCTATGTCCAC[A/C]AACAAGAGAATAGAT | 8945 |
rs142019538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440440 | GAAAGTTCCTCAATG[A/G]CTGGGCACTGTGGCT | 8945 |
rs142023043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518244 | GGCCTCCTTCTATTT[A/G]TGTCCCATATAGTTT | 8945 |
rs142036566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418853 | CCCTAATGCTCTCCC[C/T]TGACCCGCCCTCCTG | 8945 |
rs142039032 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101414340 | TGTAGCCAATGTAAC[A/G]TCATATAATGCAAGG | 8945 |
rs142077099 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101363584 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 8945 |
rs142081760 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | BTRC | GRCh38.p7 | 10:101526569 | CAGATCACTCGAGGC[C/T]AGGAGTTTGAGACCA | 8945 |
rs142108859 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405830 | CACTGCAAGTTCAGT[A/C]CTTTGAACTTCCTTC | 8945 |
rs142110490 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101370284 | TTGCCACCACGCCTG[C/G]CTAATTTTTTGTAGA | 8945 |
rs142115807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101367739 | TATCTTTTGTCCCAC[A/G]TTGTTCGTAAGATGA | 8945 |
rs142191939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519557 | AAACTCTGTGCTTGT[A/G]AAGCCTCATACGATT | 8945 |
rs142212351 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101457752 | TACATTTGATGGAAT[G/T]TTCCCCCTAAAATTT | 8945 |
rs142225715 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553575 | GGTATGGGGGATGCA[C/G]CTTCAAGCCCAGTGC | 8945 |
rs142292553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543210 | GCTCTATTATTGGGT[A/G]CCTGCGTGCTTAGGA | 8945 |
rs142299752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101430608 | CTCCTTTAATGATTA[C/G]TTTATAATGTAGACC | 8945 |
rs142319833 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101482637 | CCTGACGTCGTGATC[C/T]GCTTGCCTCAGCCTC | 8945 |
rs142327827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101383783 | TGTTGGGAAAATTTT[A/G]GCAATTGGCTAAATT | 8945 |
rs142346659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101541754 | TTTTTTAGCTTTAAA[C/T]CCTTTGCATTGCTGG | 8945 |
rs142382301 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101517929 | TGTTGAAGTAGTGTC[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs142395774 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | BTRC | GRCh38.p7 | 10:101540324 | GGTGTAGATCAAAGG[G/T]TTGGGCTTTTTTACA | 8945 |
rs142412004 | snp | C/T | 1.66693e-05 | 0.00288693 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521868 | TCATAACTGCTCTGC[C/T]AGGTATGTCTACAAG | 8945 |
rs142428571 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101486570 | TCCTAATACTAAAGA[C/G]GGGAGGTGGGGAAAA | 8945 |
rs142433652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546847 | AAATGAAAGAGATCC[C/T]AGATCTTCACAGAAT | 8945 |
rs142523207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387978 | TTCAGGTGTGAGCCA[C/T]CATGCCCGGCCTTTG | 8945 |
rs142535360 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101474600 | TTAGTCTTCCTCCTT[C/T]CCCTGTGGTTCTCTT | 8945 |
rs142559022 | in-del | -/TTCC | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101405323 | ATCAGAGAGGAAGGT[-/TTCC]TTCCTTACTTCAGAG | 8945 |
rs142699139 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101354898 | GAATGAGGACCTAGG[A/G]CTATAATGACAGTCC | 8945 |
rs142702537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101492217 | GAGTATCTAAGAGCA[A/T]AAGAAATTTAATTAT | 8945 |
rs142715313 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101456969 | ACTTATTCATAGGGG[G/T]TATGTTCCCCAGTGG | 8945 |
rs142720469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359514 | TTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAA | 8945 |
rs142837075 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442294 | TCTCTGTCTCTGTGT[C/G]TATGTGTGTGTGTGT | 8945 |
rs142845462 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101461235 | TATTAATGTTATTAA[A/T]GTTACTAATGTTGTT | 8945 |
rs142875019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485926 | GCATGTCGGATCACC[C/T]GCACAGAGAGATCAC | 8945 |
rs142881962 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417591 | ACTTTATATTTTTCC[A/T]ATTAAAACGAAGTAG | 8945 |
rs142883450 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101446109 | GTTCTCTTCCCCCCC[A/C]ACCCCCCCAACCCCC | 8945 |
rs142946291 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | BTRC | GRCh38.p7 | 10:101425785 | ACTGCACTCCAGCCT[A/G]GGCAAGAGAGTGAGA | 8945 |
rs143064603 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101507145 | CCCAAGTCTGTATCA[A/C]TGGGGCTTTTTTCCC | 8945 |
rs143084019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448622 | ATCTGAGTTATATTT[A/G]CTGTTTTCTGTTTAA | 8945 |
rs143087286 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353340 | GAGGCCATTATATTC[C/T]ACCGTTGAAGGACTT | 8945 |
rs143127569 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418622 | ATCTGCTTTTTTTTT[-/T]GCCAAACATATATAT | 8945 |
rs143150769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537917 | ACTTATCTTATTTAA[A/G]TCAAAAGATGAGGGC | 8945 |
rs143155241 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101428135 | TTGATGTAAATGGTC[A/C/G]ATATGGATTGGCAGG | 8945 |
rs143164847 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101505348 | AAGATGGCCGGGCGC[A/G]GTGGCTTACGCCTGT | 8945 |
rs143194545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443578 | TTGATCATATTAAAG[A/G]TATAGAAACAAGTAT | 8945 |
rs143251501 | in-del | -/AAAA | 0.955173 | 0.0864959 | intron-variant | BTRC | GRCh38.p7 | 10:101390765 | TTTTGTTTGTCTTAA[-/AAAA]GAAAGAAAGAAAGAA | 8945 |
rs143275330 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101468568 | CAGCTTCCTTAGATA[C/T]TGCTTTTTGGTTTGC | 8945 |
rs143308686 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101510938 | TTATCAGCCTTCTAA[A/C/T]TGATCTTTCTTCCTC | 8945 |
rs143347672 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | BTRC | GRCh38.p7 | 10:101449009 | TATAATAATAAGCCT[A/G]TATAATAATTTCTTA | 8945 |
rs143347891 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | BTRC | GRCh38.p7 | 10:101356106 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8945 |
rs143378158 | snp | A/C | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101460526 | TTACAAGGGATCATC[A/C]CAAATGTAAAATATC | 8945 |
rs143387215 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530063 | ATTGCCATTTACTGA[-/T]TTTTTTTTTTGTAGC | 8945 |
rs143463733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499862 | GTGCTTGTCCATATT[A/C]ATTTAGTTATTACAA | 8945 |
rs143469890 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101400324 | CTTAATGAGCAAGTA[A/G]TTTTCTTTTCTCTAC | 8945 |
rs143486638 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101452985 | AAAGGATTAATTAAA[A/G]TTTGTTTAAACACAC | 8945 |
rs143506618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401424 | ATAAATTTGCTTACT[A/G]AGATGGTTGATTGAT | 8945 |
rs143508413 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101404330 | CCACCGCGCCCAGCC[A/G]ATCCTAGCTATATTA | 8945 |
rs143546663 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352679 | TTTATTTTATAAATT[C/T]AGATATTTTGTACAA | 8945 |
rs143568781 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101483974 | TAGGTTTTTTTCCCT[A/G]ATTTACCCTTACCCA | 8945 |
rs143609663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101392585 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 8945 |
rs143643543 | in-del | -/CATTCTAAT | 0.0256215 | 0.110247 | intron-variant | BTRC | GRCh38.p7 | 10:101509179 | TTACTTATCTCTTTC[-/CATTCTAAT]CAAAGTGTAAACAAT | 8945 |
rs143656384 | in-del | -/ATATATATATATATAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101475923 | TCCAAGTATTTTGCC[-/ATATATATATATATAT]ATATATATATATATA | 8945 |
rs143673511 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101477290 | ACAGGTGTTAGCCAC[A/C]AGGCCCCACCGTGAT | 8945 |
rs143673816 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | BTRC | GRCh38.p7 | 10:101531814 | AAAGCTTTAAAAAAT[A/G]GTTTACTAATAAGTA | 8945 |
rs143693216 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101358855 | CCAACTACAGAGGGA[A/G]GAGAAATAATGTCTA | 8945 |
rs143693959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416989 | TCAAACTACAGAAGA[G/T]TTGTAAGTAAAATGC | 8945 |
rs143720878 | in-del | -/AATAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101381131 | TGGGTGGTGATAATA[-/AATAA]ATAACAATAATAATG | 8945 |
rs143730581 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101374839 | TAGGCTGAACTGAAG[A/G]TTGAAGATCTCTGGA | 8945 |
rs143750249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478214 | ACTCAGGTGGGAGAA[C/T]CACTTGAACCTGGGA | 8945 |
rs143763778 | in-del | -/GA | | | intron-variant | BTRC | GRCh38.p7 | 10:101538729 | TGTCCAAAATCTGAG[-/GA]GGACCTGTACACCTG | 8945 |
rs143804612 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101516873 | TATCCAGAAAACAGT[A/C]CTCCAGTAGCACCCA | 8945 |
rs143807630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413089 | TTGAAGGTGAACTTA[C/T]TAACATAAATGAGGG | 8945 |
rs143870719 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101496399 | TAGTAGTATTATGTA[A/T]GACATTTTGGATTTT | 8945 |
rs143871375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527833 | ACAAAAGAATATTAT[C/T]ACTACTTCTCAAATA | 8945 |
rs143886629 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419348 | TCAGGAGTCTGGGCA[C/T]AGCTGACCTGGGCCT | 8945 |
rs143888829 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101480424 | TTTTTTTCTTATAGG[A/G]GCTGAGAAGTCCAAG | 8945 |
rs143929420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417943 | TACAGGTGTGACCCA[C/T]CACACTTGTCCCCAG | 8945 |
rs143946272 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101356893 | TCCAGGACTTTGGGA[A/G]GCCGAGGCAGGCGGA | 8945 |
rs144036571 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101380951 | TGTACACTGAATCCT[A/G]TAAGCCATTGTAACA | 8945 |
rs144045645 | in-del | -/C | 0.0876345 | 0.190099 | intron-variant | BTRC | GRCh38.p7 | 10:101522238 | GTAGAGATGGGGTTT[-/C]CACCATGTTAGCCAG | 8945 |
rs144092688 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101395596 | CAGAATTTGAAATAA[C/T]AGTGGATTTTTTTCT | 8945 |
rs144101401 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101518695 | CAGCCACACCAGGCC[C/T]TCTTGTTCCTTGAAC | 8945 |
rs144105852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414944 | AAGTGAAAAAGTCAC[A/G]GTAAGCTAAGTTTAT | 8945 |
rs144118963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101504231 | AAACTTTATTACTCC[A/G]CCTGAAACATTAAGT | 8945 |
rs144125076 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403339 | AGGACTTGGAACCAG[G/T]CATTGGAATACCTTT | 8945 |
rs144139485 | snp | C/T | 0.000824239 | 0.020284 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479389 | AACAGCTGTGCCAGA[C/T]TCTGCTTAAACCAAG | 8945 |
rs144146653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364614 | TCATAGAGACAGATA[C/T]CCAGGAATTATAGCA | 8945 |
rs144158045 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101451639 | GCCTGCATAGACAAT[A/G]TATTTTTTCCCCCCT | 8945 |
rs144175971 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101398214 | ATAAGGTGGAAGAAG[A/G]TGGAGTTCTGTAAGA | 8945 |
rs144263629 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101512682 | CAGCTTCAGAGAAAT[G/T]CATGGTAATTTTGAA | 8945 |
rs144281261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101464992 | CCCTGAACTTGATTA[C/T]CCCATTGCTGATTTT | 8945 |
rs144292209 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101356906 | GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 8945 |
rs144321869 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101411607 | CATTTCAAACATTGT[A/G]TTTTTCATTCTGGAA | 8945 |
rs144334888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449510 | AGAGGATCTCTGGAT[A/G]AAATATTTTTGTAAA | 8945 |
rs144362541 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | BTRC | GRCh38.p7 | 10:101415486 | TTTATTTTATTTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs144393393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101445574 | TGTATGGATCACTGG[C/T]ATGTAATAATCGACT | 8945 |
rs144435640 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557319 | TTAAAGTGAATTTTC[C/T]AAGCGTCTTGTCTCC | 8945 |
rs144450465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101534239 | AACCTGAGATCCAGG[A/G]TAATCAAACTCAAAT | 8945 |
rs144463449 | in-del | -/GGTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101485380 | GCATCAGACTGGCTG[-/GGTT]TTTTTAAGCCTGAAG | 8945 |
rs144465267 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101389308 | TCAAATTCGTCTACC[C/T]CTCTCTGCCTACACT | 8945 |
rs144483033 | snp | C/T | 0.167809 | 0.236103 | intron-variant | BTRC | GRCh38.p7 | 10:101475396 | AATACAAAAATTAGC[C/T]GGCCGTGGTGGCACA | 8945 |
rs144488921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101541034 | GATTGTTCATTGCAA[A/G]TACATAGAAATATAC | 8945 |
rs144526051 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101480523 | CTGCATCCTCACATG[A/G]TAGAAGAGACTAGCT | 8945 |
rs144528159 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | BTRC | GRCh38.p7 | 10:101381284 | GGAAACTGAGGCACA[A/G]ACAGGTTGTTACTTT | 8945 |
rs144569142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384378 | CGAATAAAAAGTTTA[A/T]TTTCACGCCCTGATT | 8945 |
rs144583951 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | BTRC | GRCh38.p7 | 10:101463234 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 8945 |
rs144643304 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556145 | CTCATAACTTGTTTC[C/T]GAACTAGAAAAGTCT | 8945 |
rs144679625 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101488691 | TAAAAGCAAGTAATA[C/T]GTTATAGGCTATGTA | 8945 |
rs144680753 | snp | A/G | 0.113685 | 0.209567 | intron-variant | BTRC | GRCh38.p7 | 10:101388255 | TAACATCAACCTCCT[A/G]GGCTCAAGTGATCCT | 8945 |
rs144698143 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101491850 | GAAATCCTCTGTCTC[A/G]GAGAAAAGGCTTGGG | 8945 |
rs144737671 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101498820 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 8945 |
rs144776202 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101551309 | TCTAATGTGTGAATG[G/T]AAACATCTCTTGGTG | 8945 |
rs144776787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101441046 | TAGATTTGCATTTAA[A/G]CTATGAGAACCCACT | 8945 |
rs144822884 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101494998 | TTGAAAAAGGTCTCT[C/G]TCATCCAGGGGGTTA | 8945 |
rs144826615 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101392820 | TAAGCTTCCGCACCC[A/G]ACCAATTAAAAGTTT | 8945 |
rs144886778 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101412767 | AGTCCACACATGACT[A/G]TGTGAAAAACAGATA | 8945 |
rs144992221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506762 | AGTGCTCTAAACAAC[C/T]GAAGTTTACTTATTT | 8945 |
rs144999600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405816 | TAGTCAACAACATAC[A/G]CTGCAAGTTCAGTCC | 8945 |
rs145060990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414036 | TACAATTCAGTAGTT[G/T]TAGCACATTCACATC | 8945 |
rs145111160 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101520121 | ACATTATATTTTCTA[A/C]GTATTTGCTTGTATT | 8945 |
rs145115048 | in-del | -/GACTTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101518851 | ATCTCTAACCACTTA[-/GACTTA]AATAATCCTATTAGT | 8945 |
rs145125387 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527790 | CTCTCTCTCTCTCTC[A/T]CACATACACACACAC | 8945 |
rs145126380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522778 | AACCTATTTTTACCC[A/G]TACATAGGTCCAAAT | 8945 |
rs145150322 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101525194 | CCTCAGTACAGATTT[G/T]GGTGGTGGAGAACTT | 8945 |
rs145150425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459077 | GCAGCTGGGATTACA[C/T]GCATATGCCAAAGTA | 8945 |
rs145175060 | snp | G/T | 0.0640965 | 0.167152 | intron-variant | BTRC | GRCh38.p7 | 10:101371171 | CCACTATTCTTTTTT[G/T]TTTGTTTGTTTGGTG | 8945 |
rs145188677 | snp | C/T | 0.029116 | 0.117091 | intron-variant | BTRC | GRCh38.p7 | 10:101464548 | TCCCCCCCACCCCCC[C/T]CATGGTGCTTTGAAA | 8945 |
rs145189432 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101499522 | TATGAGCCACCATGC[G/T]TGGCCACTATGCAGT | 8945 |
rs145195999 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101369688 | GACACACCACACACA[C/G]AGGTGCACATTGCAC | 8945 |
rs145211418 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101442164 | CTAGCTCCAGTTCCT[C/G]AAGATGGTGAACATC | 8945 |
rs145272049 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101526967 | GTTGTTCTCTTAACA[A/G]TACTATTTCATTAGA | 8945 |
rs145291027 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | BTRC | GRCh38.p7 | 10:101529986 | TTTACTAGCTTCCAC[A/G]CCGTGTTTGGTGGGT | 8945 |
rs145309626 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495780 | TTCACGAAGTGAACA[C/G/T]ACCTGTGTGATTACC | 8945 |
rs145348271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101436883 | GTGAAATGTTAAAAT[A/G]GAACAATACAGGAAA | 8945 |
rs145348316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502956 | ATCACAACTTATGCC[C/T]TTACTATGTGCCAGG | 8945 |
rs145359940 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101541039 | TTCATTGCAAATACA[A/T]AGAAATATACTTTTA | 8945 |
rs145367680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101433249 | ACTTTACATACATAT[A/G]TAGATGTTTATTATA | 8945 |
rs145374123 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532787 | GTGTGTGTGTGTGTG[C/T]GTGCGCGTGTGCGCG | 8945 |
rs145388143 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101381848 | GAACAAGAGCATCCT[C/T]ATTCCTAACCTCAAT | 8945 |
rs145416337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101551784 | CAGAGGACACGGTTC[A/G]TCGTTCCTCAGCCAG | 8945 |
rs145431733 | snp | A/G | 0.000339789 | 0.0130299 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521664 | CCAATGGCACTTCCA[A/G]TATGATTGTGCCCAA | 8945 |
rs145451603 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460331 | CATGTATTGCCAGTC[A/G]CCTCATTTGTCAAGC | 8945 |
rs145471356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386861 | CCCCTAATTTAAGAT[A/C]ATGAAAATAGCCTCA | 8945 |
rs145494801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101444838 | GTGAACAAATTTCCT[C/T]TCTCAAGAGCATGGC | 8945 |
rs145501336 | in-del | -/CTTCC | 0.0225045 | 0.103662 | intron-variant | BTRC | GRCh38.p7 | 10:101359091 | TGATCTCCTGCGTGA[-/CTTCC]CTTAATGATGTCACT | 8945 |
rs145512054 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101390985 | ACAAATGGTTCTTTA[C/T]CAAATTTAGAAATTT | 8945 |
rs145560962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101452694 | ATCTAGTTGTTAGCA[C/T]TGTGCTTGGAATTGG | 8945 |
rs145624314 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101420074 | CATATATATATATAT[A/C]TCATGAATATATTAT | 8945 |
rs145672979 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101523224 | ATAAATAAATAAATA[A/G]ATAGATAAATAAATT | 8945 |
rs145694691 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | BTRC | GRCh38.p7 | 10:101460924 | TGTTGTTGTTTTGAG[A/T]CGGAACCTTGCTCTG | 8945 |
rs145701027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367746 | TGTCCCACATTGTTC[A/G]TAAGATGATTCATTC | 8945 |
rs145807351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460330 | GCATGTATTGCCAGT[C/T]GCCTCATTTGTCAAG | 8945 |
rs145817606 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101402645 | TTTTATTGCTGTAAG[A/G]TAGTTAGAAATATCT | 8945 |
rs145833672 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101386258 | AACCAAGCAAATGCC[C/T]AGCAAGGTCAGTTTA | 8945 |
rs145838738 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467431 | CTTTGTTCTGATAAT[A/C/T]GCTCGAGAAAACCCA | 8945 |
rs145840992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467288 | GATTTGATTGATGAG[A/G]GAAAAAGGTTTAATG | 8945 |
rs145842754 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | BTRC | GRCh38.p7 | 10:101371699 | TTTTGACCTTTGTGA[A/C]TAATGCTGCTATTTG | 8945 |
rs145847638 | snp | A/G | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406101 | AAATTGTTAGTAGTG[A/G]TACATATACTTTTAG | 8945 |
rs145937846 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101430948 | CTGTTTTATTTATAT[A/C]TTGATTAACATTTCT | 8945 |
rs145949635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547189 | ATTGTAATTTGAGGA[A/G]CATCTGTATTTTAAA | 8945 |
rs145949879 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101381013 | GGTACGGTAAAAATA[A/C]AGTGTTATAATTTTA | 8945 |
rs145959463 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101484646 | GCATGTCATATGGTC[C/T]GTTCTTCACACAGGC | 8945 |
rs145960104 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385094 | CAAAATTAGCGTGGC[A/G]TGGTGGTGCACACCT | 8945 |
rs146072754 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | BTRC | GRCh38.p7 | 10:101461340 | TTGACTAGCAGATTT[C/T]TAGTACTTATGAACT | 8945 |
rs146072899 | snp | A/G | 0.122064 | 0.214785 | intron-variant | BTRC | GRCh38.p7 | 10:101404282 | TGATCCGCCCTCCTC[A/G]GCCTCCCAAAGTGCT | 8945 |
rs146084057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101409810 | GTTTATCTGTTTATT[C/T]GTTGATAAGTATTTT | 8945 |
rs146089700 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365032 | CAAAAGGCCGAGAAG[C/T]GATTTTAATTCTTTT | 8945 |
rs146159129 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | BTRC | GRCh38.p7 | 10:101483330 | CCGGGCACGGTGGCT[A/C]ACACCTGTAATCCCA | 8945 |
rs146182312 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101485010 | TCTAGATGTGCGTGC[C/T]GTTTAAGAAAAATAC | 8945 |
rs146193429 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101423983 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG | 8945 |
rs146193474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489630 | AAATTTTATTCTTGC[A/G]TCATGACTTCAGCTT | 8945 |
rs146205196 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101430185 | CTTTTGGGATTCTCT[C/T]TGGGGTTAAAGCCAG | 8945 |
rs146298732 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101513163 | CTGTATTGGAGAATG[A/G]TAGAAGAAAGGGGCA | 8945 |
rs146302660 | in-del | -/GATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101436633 | AAAAAAAATAGATAG[-/GATA]ATAGATAGATAGATA | 8945 |
rs146310321 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101451476 | AGTTCTTCTAAATAC[C/T]GAATGTGTCATGCGC | 8945 |
rs146310755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518269 | TAGTTTTAAAGGACC[A/G]CATAGCAGTGGTCCT | 8945 |
rs146315079 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | BTRC | GRCh38.p7 | 10:101359061 | TTTTGAGGTTAACTT[C/T]GGAAGGCACTAACAT | 8945 |
rs146322119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455528 | TTAATTCTAACTGCA[C/G]GTTAGGCGTAAGGGG | 8945 |
rs146326567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363741 | GAAAGCTTCATATTA[A/G]ATCTTGATGAATAGA | 8945 |
rs146391270 | in-del | -/TG | 0.030278 | 0.119257 | intron-variant | BTRC | GRCh38.p7 | 10:101484158 | ATTGGTTGTTGTCAC[-/TG]TGTTTTTTTATTTGA | 8945 |
rs146421743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101377031 | TAAACCACAATCAGG[A/G]TAAGAACAATTGTAT | 8945 |
rs146435684 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531321 | TTATCCTAAAATTAT[A/G]CAAGACATTGAGGTA | 8945 |
rs146442260 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101486624 | CTTTATTTAAAAGGC[A/G]TCGGTTTCTATTATT | 8945 |
rs146442281 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | BTRC | GRCh38.p7 | 10:101421933 | GCCACAGTAAACATA[C/T]GTGTGCATGTGTCTT | 8945 |
rs146492575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101448041 | AATCGAAGATAGTTA[C/T]GGTGTGGAAAGCAAT | 8945 |
rs146503724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101451647 | AGACAATATATTTTT[C/T]CCCCCCTGAGGTCCC | 8945 |
rs146505169 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101426352 | TGACTATATTCAAGT[A/G]TAGTTTTCATACCCA | 8945 |
rs146545459 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101398364 | CTGGAGTACAGTGGC[A/G]CGATCTCAGCTCGCT | 8945 |
rs146624152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416456 | CTTTTCACAGACATA[A/T]CCCTTTGGTTCAGTT | 8945 |
rs146624668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101480730 | CAAAATATAACCATC[A/G]AAATCATACATATAA | 8945 |
rs146665704 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | BTRC | GRCh38.p7 | 10:101419170 | CACACACCACCATGC[C/T]TGGCTAATTTTTATA | 8945 |
rs146729706 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101500296 | TGTACGCAATCATAA[C/T]ATGATGGTGTTTGTG | 8945 |
rs146741363 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101506323 | ACATGGTGAATGTTA[A/C]ATACAGTTGCTCAAG | 8945 |
rs146758217 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352826 | GGTTCAAGCAATTCT[C/T]ATGCCTCAGCCTGCC | 8945 |
rs146783646 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101447534 | CTAATTCTGTACTGT[A/G]AGAACAACTACTATG | 8945 |
rs146804594 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101385615 | CTTTCTTTCTTCTTC[-/TT]TTCTTTTTTTTTTTT | 8945 |
rs146810440 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101526657 | TGGTGGCGTGCACCT[-/G]TAATCCCAGCTACTG | 8945 |
rs146852288 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101528001 | TGCTAAGAGTGCTGG[A/G]ACCAGCCTTGGGGAT | 8945 |
rs146865275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101425270 | TTTTTTTTCTGATTC[A/G]GGTAGTAGAAAACAT | 8945 |
rs146866369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533121 | TATCAGCTCTGCTCT[A/G]TTCTTTGTCATAGAT | 8945 |
rs146868221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101371207 | TTTTTCCCCCAGAGA[C/T]GGAGTCTTGCTCTGT | 8945 |
rs146894866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504296 | CCTCTTGATGTTTAT[C/T]GTGTGGGAGAGGATG | 8945 |
rs146906928 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407048 | TACTTTTAAATTTTC[A/T]TGTAGCCACATTGAA | 8945 |
rs146928555 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532779 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGCGCG | 8945 |
rs146941964 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | BTRC | GRCh38.p7 | 10:101516162 | AGGCTCAGCTCCAAC[A/C]GTGTTATAAGCTCAT | 8945 |
rs146942703 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101354947 | GTTGACTGTAAGCTA[C/G]AATTACAAATGTCAG | 8945 |
rs146952782 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | BTRC | GRCh38.p7 | 10:101361308 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 8945 |
rs147011752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101536221 | GTGACTTCAGGAAAC[C/T]GCTTTCTTAGCTTGG | 8945 |
rs147048505 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101434754 | CCTGTGAAAAACCAC[G/T]GCTTAAGAACAGCCT | 8945 |
rs147048965 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377708 | ACAAAATATTTGATA[C/G/T]GCCTAACTTTAACAT | 8945 |
rs147049360 | in-del | -/AAAACA | 0.0763149 | 0.179815 | intron-variant | BTRC | GRCh38.p7 | 10:101475539 | GTGAGACTCCGTCTC[-/AAAACA]AAAACAAAAACAAAA | 8945 |
rs147058886 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101383562 | TGGAGTGCAGTGGTT[C/T]GATCCTAGCTTATTG | 8945 |
rs147117161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101453509 | CAAACAGGTTCAGGC[C/T]CTGTTGCACCATCCA | 8945 |
rs147156551 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525210 | GGTGGTGGAGAACTT[G/T]AATTGGGAAGCCCTT | 8945 |
rs147192570 | snp | A/G | 7.01176e-05 | 0.00592063 | intron-variant | BTRC | GRCh38.p7 | 10:101532467 | AGAAAGGTAGCAGAG[A/G]GAGCAAGAGTGACCA | 8945 |
rs147199567 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101473773 | GGCCAATTTTTTCTA[C/T]TTTTTGTAGAGACAG | 8945 |
rs147203954 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101375319 | GCCATATAAGATGCA[C/T]CTGCTTCCCCTTTGC | 8945 |
rs147209394 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101478550 | AATCCCAGCACATTA[G/T]AAGGCTGAGGCAGGA | 8945 |
rs147236188 | snp | C/T | 4.94328e-05 | 0.00497131 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550822 | CAAGCTGAACCCCCC[C/T]GTTCCCCTTCTCGAA | 8945 |
rs147306435 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101497839 | ATCTTGGCCAACATG[A/G]TGAAACCCCATCTCT | 8945 |
rs147307897 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101395832 | TGAATAATCTTTTAC[A/G]TGCCTGTAGGGGACT | 8945 |
rs147318257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101403461 | CCATTATTTTGTTGA[A/G]GATTTTTGCCTATAT | 8945 |
rs147395156 | in-del | -/CGCG | | | intron-variant | BTRC | GRCh38.p7 | 10:101532801 | TGTGCGCGTGTGCGC[-/CGCG]GCGCGCGCGCTTAGC | 8945 |
rs147402698 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | BTRC | GRCh38.p7 | 10:101519793 | CTGAGGTTGGGAGTT[C/T]GAGAACAGCCTGACC | 8945 |
rs147412816 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101524710 | TAGAAAGTTTTAATA[A/T]AAATTGTACCATTAC | 8945 |
rs147423309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101369057 | TCTTTTTCGTTGTTG[C/T]CACTGTAGTGGATGA | 8945 |
rs147520006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101445699 | GAGTTGTGTATAATC[A/G]CTTTGGTTTAATCAA | 8945 |
rs147529749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449149 | CTTGGGATGGTTTTA[C/T]GTCTCGGGATATTAG | 8945 |
rs147538862 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101395196 | ACCAATACAGCAAAC[G/T]CTAAGGAAAGAAGAA | 8945 |
rs147558746 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101516651 | ATGACTTGATCATTG[A/G]AAGTATCACAAAGTC | 8945 |
rs147568884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453190 | ATTAATCCAATTACT[A/G]ATTTACCATTGAAGT | 8945 |
rs147578514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459186 | GGATATAATTTAGCC[G/T]GATGATCTAGGAAAA | 8945 |
rs147589960 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101369795 | CCACAGGGTTCGTTC[A/G]ATAATTTCATAATTG | 8945 |
rs147611816 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101464673 | TTTTATCTCCATTCT[C/G]TTTGTGAAGAGCATG | 8945 |
rs147631821 | in-del | -/GGGGAGG | | | intron-variant | BTRC | GRCh38.p7 | 10:101523530 | ATCATTACCTTGTTA[-/GGGGAGG]GGTTTTGGTTGTTGT | 8945 |
rs147673601 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553166 | ACAGGACCCATTAAA[A/G]TTGCGGTATTTAACG | 8945 |
rs147681042 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101486271 | TTTCCCAATAAACTC[C/T]GACTTGTAATAACGT | 8945 |
rs147684612 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101386922 | GTTTTTACGTTTAGA[A/G]TTTTAGTCTTTCTAG | 8945 |
rs147694760 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101390993 | TTCTTTATCAAATTT[A/G]GAAATTTTACTCTTG | 8945 |
rs147785624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515790 | TGCTTGGATTATAGG[C/T]GTGAGCCACTGCTCC | 8945 |
rs147866010 | in-del | -/C | 0.209084 | 0.246629 | intron-variant | BTRC | GRCh38.p7 | 10:101440354 | GGGGCATTGAATTTA[-/C]CAAGTAAAGTTTTAA | 8945 |
rs147872361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486817 | ACCAGGACAAATCTT[C/T]TGAAGATATTATCTC | 8945 |
rs147893057 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101434638 | AGACACTTTAAAAAA[A/C]TGAGCAGGAACCAGG | 8945 |
rs147929471 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | BTRC | GRCh38.p7 | 10:101441076 | TGTCTTGACTCAGTG[A/G]GGGAGTTTTCAAAAA | 8945 |
rs147973030 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101490006 | AGTCTAGTCCTTTGG[C/G]ACTTACCCAATACAC | 8945 |
rs147997023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402463 | TTTAGAAGGCACCCA[A/G]ATTTTAACAATTGTA | 8945 |
rs148005424 | in-del | -/TTCT | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101481314 | GGGCCTTTAAAAATA[-/TTCT]TTCTTTCTTTTTTTC | 8945 |
rs148019597 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101502995 | CTGAATACCTTTATA[G/T]GTATTATTTTAATCT | 8945 |
rs148022320 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534832 | CCGGAGGGTGCTGGT[C/T]GGACACCGAGCTGCT | 8945 |
rs148028490 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101484062 | CAGATTCCTGGCCCA[G/T]ATAAGAGAAGTTTTT | 8945 |
rs148048910 | in-del | -/TCTCTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101442262 | CTAATTGAATTAGAA[-/TCTCTC]TCTCTCTCTCTCTCT | 8945 |
rs148090504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417160 | ATTATTGGCATATTA[C/T]TTTGTCATCTAATCC | 8945 |
rs148145149 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101517020 | AAGCTTATAAGCCTG[C/T]CTGTGTGTTAGTTCT | 8945 |
rs148151903 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363011 | TTGAGTATCTGTGGA[-/T]TTTGGTATCCGATGG | 8945 |
rs148186933 | in-del | -/TT | 0.0314385 | 0.121371 | intron-variant | BTRC | GRCh38.p7 | 10:101444099 | AAGGAAATGGTATAC[-/TT]ATGTTCATATCAGAT | 8945 |
rs148208130 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101448659 | ATTTTCTCTCATTCT[A/G]GTTTTTTCATTTCTG | 8945 |
rs148209129 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353973 | GTTTTTTTCCTGGGG[A/G]AAGTTCCAGAACTAC | 8945 |
rs148243196 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101428904 | CTCCTGGGCTCAAGC[A/G]ATCCACCCATCTCAG | 8945 |
rs148252455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101379323 | AGGTTTATATGTGGT[C/T]ATGTTACAAAGGATT | 8945 |
rs148303736 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | BTRC | GRCh38.p7 | 10:101470392 | GGCTGGAGTGCAGTG[A/G]CACAATCTCGGCTCA | 8945 |
rs148354798 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101460783 | ATAATTTCATGCTTG[G/T]ATGAAAATTTTCAGA | 8945 |
rs148363852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407380 | AAGTTGAAATTTTCA[A/T]AATGTATTTTATTTA | 8945 |
rs148399397 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101390085 | TTTGTCTATTATTTC[C/T]ACTAGAAAAGAAAAT | 8945 |
rs148403256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474416 | TCCCTCTAACTTGAT[A/G]GAAGTCAAACTCTAA | 8945 |
rs148407255 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101376870 | AGGCATTCCACTCTC[A/G]TTCCATTTTACTCTT | 8945 |
rs148458342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101464095 | TTGGGAAGTAGGAAC[A/G]CTCTGCCCACTATAC | 8945 |
rs148478790 | in-del | -/GTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101519394 | CCTCAGCTCATTCTT[-/GTA]GTAGGCAGAATTCAG | 8945 |
rs148494365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101410545 | CTTGAATCTGGGAGT[C/T]GGAGATTGCAGTGAG | 8945 |
rs148550587 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101485924 | ATGCATGTCGGATCA[C/T]CCGCACAGAGAGATC | 8945 |
rs148605863 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101439332 | GTAAACAATAATACT[G/T]TGGAAAAAAAATAAA | 8945 |
rs148614328 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101418714 | ATTATTATTATTATT[A/T]TTTTATTCTGGGGTA | 8945 |
rs148636474 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101525764 | GTCTTGGGGGGTTTG[C/T]TGGTTGTTAGCTTTA | 8945 |
rs148651181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369950 | ATGCCGTCCTTGACT[G/T]ACTTAGGCTCCAAAA | 8945 |
rs148665361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518777 | TAGACCATTCTTCCT[C/T]GCTGTCTAGTCCTCA | 8945 |
rs148691756 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101533704 | ATCAAAAGTAACTTT[-/A]AAAAAAAAATAGACC | 8945 |
rs148701791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101457467 | GCTACCAGAAAGGTG[C/T]ACAATTGAAAACTAT | 8945 |
rs148754040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450485 | TATCAGAGTATCTCA[C/G]TGCTTAGTTGAGCTT | 8945 |
rs148762369 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101541283 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTTTC | 8945 |
rs148762670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101433265 | TAGATGTTTATTATA[C/T]TTCTATTTTGTGAAA | 8945 |
rs148764343 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101396582 | ATATGTGGTATAGAA[C/T]TATTTTCATTTTTGA | 8945 |
rs148796605 | in-del | -/TG | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101427034 | TTCCTTCCGAATGAC[-/TG]GTGAGATTTTTTTCT | 8945 |
rs148832907 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364979 | AGGACATATCAGATA[C/T]TAAACTGATGAGAAC | 8945 |
rs148859409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452939 | ACAGCTTCTGAACTT[A/G]AATGACCTAAGTTTT | 8945 |
rs148866054 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | BTRC | GRCh38.p7 | 10:101544277 | TACCTTTTCTATTGC[C/T]TCCCATTCCTTTGTA | 8945 |
rs148870059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101401250 | CTAATCAGAGGTAAA[C/T]TGCAGTTTTACTCTT | 8945 |
rs148882139 | in-del | -/CA | | | intron-variant | BTRC | GRCh38.p7 | 10:101437420 | GTGTGCCTGTGCGTG[-/CA]CACACACACACGCCC | 8945 |
rs148894811 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534768 | TGACCTGCTCCAAAG[A/G]TCGTTCCATTGCTGT | 8945 |
rs148920181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101492169 | GTTTTATACCTCAAA[C/T]ATCACTTCTCTAATT | 8945 |
rs148954953 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101476921 | GCACTAACGTCAACT[A/G]GGGCCTTGTTAAAAA | 8945 |
rs149015483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412930 | AATTGGCCAACAGAT[A/T]TGAAACAAAGTAACA | 8945 |
rs149025062 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101361975 | ATTTTTTTTTCTTCC[C/G]CCTTGAGACGGAGTC | 8945 |
rs149121771 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101499727 | TCTTCCATCCTTACT[A/G]TGTAGGCCTACGAGA | 8945 |
rs149131504 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101442240 | TCTTTTCTGGAGTTG[A/C/T]GACTGCACTAATTGA | 8945 |
rs149145606 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101508937 | AAAAAAAAAAAAAAA[-/CT]AAAAGTAGAATGTTA | 8945 |
rs149161195 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101422160 | TTTTTAATGATCACC[A/G]TTCTAACTGGCGTGA | 8945 |
rs149162617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530645 | CATATTCCATTTGTT[C/T]ACTGATATTATAATA | 8945 |
rs149225229 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | BTRC | GRCh38.p7 | 10:101460493 | TATAGCATGCTTTTT[C/G]TTTAATTTTAGGGAC | 8945 |
rs149229640 | in-del | -/TTTTA | 0.401037 | 0.199218 | intron-variant | BTRC | GRCh38.p7 | 10:101388331 | CCACACCCAGCTAAT[-/TTTTA]TTTTATTTTATTTTA | 8945 |
rs149233586 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556747 | GGTGGAACTTAATGC[A/G]TTGATCTTTAGAAGC | 8945 |
rs149234038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445472 | AAGACATAAATTTAC[G/T]CAAGCCAACTGTAAG | 8945 |
rs149271025 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101389246 | ACTTTTTCTTATGCC[A/G]ATATGCAATTCACAA | 8945 |
rs149274045 | in-del | -/AC | | | intron-variant | BTRC | GRCh38.p7 | 10:101385731 | CCTTCCTCTTCCCAG[-/AC]ACACACACACACATA | 8945 |
rs149320258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524649 | GGAACAATTTGATGG[C/T]ACCCATTAAAAACAC | 8945 |
rs149321432 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101483705 | GAATTCTTTCTCCTG[A/G]TTATGGCCCTGTGTT | 8945 |
rs149325991 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364832 | TCTTTTTTTTTTTTT[G/T]TTGTATCCCCGGAGC | 8945 |
rs149330036 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | BTRC | GRCh38.p7 | 10:101462367 | TTTCTAGAAGAAAAG[A/G]CCATTGTTAATAATA | 8945 |
rs149386813 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101416955 | TAATTTATATTCCAT[A/G]TTTTATTTTTAAACA | 8945 |
rs149414405 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389175 | CATACTAATAAATGG[G/T]GCCACCATTTATCCA | 8945 |
rs149417971 | snp | A/T | 0.000115478 | 0.00759775 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550843 | CCTTCTCGAACATAC[A/T]CCTACATCTCCAGAT | 8945 |
rs149444642 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101496383 | GCATTCTGGTGATAC[A/G]TAGTAGTATTATGTA | 8945 |
rs149448564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395113 | GCTAATGTAGAAGTC[A/G]TTATCACTAGGTGGC | 8945 |
rs149480420 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | BTRC | GRCh38.p7 | 10:101374346 | TCATGTGTTTATTGC[A/G]GCATTATTCACAATA | 8945 |
rs149499745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488394 | ATTGAGAACTGAATA[G/T]CAATCAAGTAAGGTG | 8945 |
rs149540579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518476 | AATGGAATGCAACTT[A/T]CTCCCCATTCTCTTA | 8945 |
rs149541943 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101414791 | AATAATATATATAAT[A/G]TATATTTTTTAAATA | 8945 |
rs149595118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512263 | TAAATTAATTCAGCA[C/T]TTAATCATTATATCC | 8945 |
rs149596979 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | BTRC | GRCh38.p7 | 10:101372105 | TTCTCAGTAGCTCCA[G/T]TGGTCTATTCTTGTG | 8945 |
rs149604570 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101449420 | AAATCTACAGAGGTC[A/G]AGTTACAAAAATAAC | 8945 |
rs149626639 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | BTRC | GRCh38.p7 | 10:101368088 | GAGGTGGGGCCTGGT[A/G]GGAGGTGTTTGGATT | 8945 |
rs149690847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101423966 | CGGGTGAGGTGGCTC[A/G]TGCCTGTAATCCCAG | 8945 |
rs149695250 | snp | A/G | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515615 | CTCCCGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 8945 |
rs149706558 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359984 | ATGTGGAGTAAAAAT[A/T]CAACTTTGAGTAGTT | 8945 |
rs149731693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452232 | TTTCTGCATACTAGC[A/G]TAAATGCACAAGGCC | 8945 |
rs149784019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447024 | CCGGTTACAAAGCAA[A/T]AGAAGCATGCAGCTA | 8945 |
rs149794138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391657 | GAAATTTGCTCTCTA[A/G]AACAGTAGCCTCCTA | 8945 |
rs149835101 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101549464 | TGACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 8945 |
rs149849731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386024 | CAGGAAAAATGGTAC[A/G]GAGATGACTTGGCTG | 8945 |
rs149854223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466968 | GGGCATAGCTCCTTT[A/T]TACAGTTGGATGAGT | 8945 |
rs149903447 | snp | A/G | 3.30907e-05 | 0.00406746 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526190 | GAGGCCTGGCAGAAC[A/G]AAGAGGATGGTGAGC | 8945 |
rs149910957 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101417650 | TTTAAGTATCCTCCT[C/G]CTTATCAAACTTACA | 8945 |
rs149918895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405813 | TGCTAGTCAACAACA[C/T]ACACTGCAAGTTCAG | 8945 |
rs149941540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506594 | AAGTGTAACAGTCAT[G/T]CTGTACCAAGCCAAG | 8945 |
rs150047738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491551 | ACTACAAAAAAATTA[C/G]CTGGGTGTGGTGGCA | 8945 |
rs150057603 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101433039 | TTGTCCAGTCGCTAA[A/G]TCTCTCAGGCAAGCA | 8945 |
rs150061719 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101521439 | CAAACTTTTGGAAAT[A/G]GATGCTTAGTCTTCT | 8945 |
rs150096739 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101503642 | CATTTACTTCATTCA[C/G]TGCAGCTAAGAGAAG | 8945 |
rs150106849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101445014 | TGGGGCAGGAGGGTA[A/G]CTAAATTGTGGTTAC | 8945 |
rs150149003 | in-del | -/TTG | 0.376592 | 0.215579 | intron-variant | BTRC | GRCh38.p7 | 10:101396754 | AGGGTTTGTTGATGT[-/TTG]TTTTTACATGATGAA | 8945 |
rs150159982 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101543912 | CATCTTTTAAGATTT[G/T]TTTGTTTGTTTGTTT | 8945 |
rs150171421 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101384248 | ACAGAAGTTGGCCAT[C/G]AGCCCTCCTTCTTTG | 8945 |
rs150209730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535549 | CACAGATCATACAAG[A/T]CTTCAATTTTGTTAT | 8945 |
rs150222199 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101475613 | ATCTCTACTATTTTC[C/T]CCATTTTTTCTTAAA | 8945 |
rs150222832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101377420 | CATGAGGGAGAATTG[C/T]GTGATAAATGTAGGT | 8945 |
rs150243767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517602 | TAAGTAAATATGCCA[A/G]AGATCCATCAAATTA | 8945 |
rs150253386 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101454973 | TCATAGAAATAAAGA[G/T]CCACTAAAAATATTT | 8945 |
rs150307904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101448864 | GGCATACCCTTCAAT[A/G]TCTATGCTGAGACAT | 8945 |
rs150308766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411840 | TTTTTGAATATTTGT[A/G]TTTTAAAAATCTTTT | 8945 |
rs150318482 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394661 | CCCTATTTCAGAGAG[A/C]GTAAGGGTTAAAATT | 8945 |
rs150357192 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554377 | CCGTGATCAAGGTAG[C/T]TTAAGAGAGATGGTC | 8945 |
rs150368873 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101487720 | GGATCCTACCCAGTC[A/G]GAACACTGAAATTAA | 8945 |
rs150420896 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101482330 | CTGGCCAAGTTTTTT[A/C]TTTTTTATTTACATG | 8945 |
rs150427100 | snp | A/G | 6.62142e-05 | 0.0057535 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535435 | TTGCAGTACAGGGAC[A/G]GGCTGGTAGTGAGTG | 8945 |
rs150431167 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101420386 | GATCCGACAGCTTGC[A/C]CTTGGCTGCCCCTTC | 8945 |
rs150465950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511126 | TGAAATCTAAACTCT[A/G]TAGGATGGCCTAGAA | 8945 |
rs150487342 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101416332 | TTTTTTAATTTGGCC[A/G]TTTGATCCCTTTGCT | 8945 |
rs150537044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423691 | AAAGTACTAATAATT[C/G]TTTGACAAGAAGGTA | 8945 |
rs150589062 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | BTRC | GRCh38.p7 | 10:101417554 | ATTAAGATATCAGGG[G/T]TTTTTTCCCACTATA | 8945 |
rs150614343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523981 | TTAAGGAATGTGAAC[A/G]TTTTAAGGCTTTTAA | 8945 |
rs150623008 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | BTRC | GRCh38.p7 | 10:101506001 | CTCACTGCAACCTCC[A/G]CCTCCAGGATTCAAG | 8945 |
rs150625153 | in-del | -/T | 0.29789 | 0.24537 | intron-variant | BTRC | GRCh38.p7 | 10:101383392 | TTCTATAAGTCTTCC[-/T]TTTTTAAAAAAAAAA | 8945 |
rs150632754 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101446404 | GGGCCAAAGGCAGAC[C/G]TTTTCCTCCCAAAGA | 8945 |
rs150679768 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101362690 | GTGAGCCACCACGCC[C/G/T]GGCCAGAAGAAATTT | 8945 |
rs150680207 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | BTRC | GRCh38.p7 | 10:101548487 | CTGGGCTCAGTGGCT[C/T]ATGTCTGTAATCCCA | 8945 |
rs150683609 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | BTRC | GRCh38.p7 | 10:101440714 | GTTGACAGAGTGAGA[C/T]TCCATCTAAAAAAGA | 8945 |
rs150732916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539259 | AGCCAAGGGCCCAGA[C/T]TGATAAATGCTGCTT | 8945 |
rs150799375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471288 | AACACTTTGGGAGGC[C/T]GAAGTGGGAGGATCG | 8945 |
rs150835705 | snp | A/G | 3.55025e-05 | 0.00421308 | intron-variant | BTRC | GRCh38.p7 | 10:101414652 | ATGTTAATTGCTCCC[A/G]AAGACCTTCCAGTGC | 8945 |
rs150893457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490688 | TTTCTCATCTTCCTC[C/T]TCTTCCTACCTCTTG | 8945 |
rs150898214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356461 | GCTTTGTACCAGTGA[C/G]TTATGTTTTGATAAT | 8945 |
rs150928693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474700 | TCAAGCCAATAGACT[A/G]TGGCTTTCAGATTGA | 8945 |
rs150937644 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant | BTRC | GRCh38.p7 | 10:101358821 | CAAGAATGTCACTGT[-/G]GGTCAAAGCCAGTCA | 8945 |
rs150938303 | snp | C/T | 0.1652 | 0.235179 | intron-variant | BTRC | GRCh38.p7 | 10:101415626 | GGCTCACTGCAACCT[C/T]TGCCTCCTGAGTTCA | 8945 |
rs150989383 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515116 | ATGCACCACCACACC[C/T]GGCAAATTTTTGTAT | 8945 |
rs151034819 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101435998 | TTCCCAGTAGCTCAA[A/G]TTGAAACCACAGCAT | 8945 |
rs151087351 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101426019 | TTTGTCAGAAACTGA[C/T]CAATCAGAATGGCCC | 8945 |
rs151116235 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510524 | AAAAAAAAACAAAAA[-/G]AAAAAGTCGTTGTTA | 8945 |
rs151138500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526737 | ATTTCTTGCCTTTAT[C/T]TTATGCCTCTGGTGT | 8945 |
rs151147415 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101507533 | AGATGAAAGAGAGGT[A/G]TTTGTCAGCTTCTCA | 8945 |
rs151148262 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101465203 | AGTAGGATTTGCATC[G/T]CATTAACTTGAGATT | 8945 |
rs151203144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101458816 | CATATTAAAAGGCAC[A/G]TAATCTTAAGGTGGC | 8945 |
rs151209219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444110 | ATACTTATGTTCATA[C/T]CAGATATATCTCATC | 8945 |
rs151213750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101405049 | TTTTGGGTTATATCC[A/G]CCCATGTGCAGCTTG | 8945 |
rs151232683 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554024 | TCTCTCTCTTTCTTC[C/G]CCACACCCAAGAGGA | 8945 |
rs151245421 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101387751 | CTGAAGTGCGGTGGC[A/G]CGATCTCTGCTTACT | 8945 |
rs151258499 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527788 | CTCTCTCTCTCTCTC[A/T]CTCACATACACACAC | 8945 |
rs151262952 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | BTRC | GRCh38.p7 | 10:101541969 | AGTGTTCCCTCATCT[A/G]TTTTCTAAGAGTTTG | 8945 |
rs151289382 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526042 | CATATTGCTGAGAAC[A/G]TTCTGTCATACCTGG | 8945 |
rs151298538 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101482061 | GTCTCACTTTGTCAC[C/T]CAGGCTGGAGTGCGG | 8945 |
rs151299947 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101382850 | TTTTGGAAAGACATT[A/T]CATGGGCTTTATCCT | 8945 |
rs180677993 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101364690 | CAGGAAGTACTACAC[C/G]AAACTGTTAATGTGG | 8945 |
rs180678188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370817 | GCTCAAGTGATTCAC[C/G]TGCCTCTGCCTCCCC | 8945 |
rs180682476 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101411532 | TTATTTTTGCTTCCT[C/T]GGGTTCACTGATCTT | 8945 |
rs180691581 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101391651 | ATTTGGGAAATTTGC[G/T]CTCTAGAACAGTAGC | 8945 |
rs180710045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354397 | AGGAGGCTGGGGGTT[A/G]CGGAGCGGACCCAGG | 8945 |
rs180775448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101547100 | AAGCTATGAAGTTCA[A/G]TAGGTTAGGCAGATC | 8945 |
rs180789302 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557427 | ATAATCTGACATGAG[A/G]AAACAAGATTGAGAG | 8945 |
rs180805830 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101526688 | TAGAGGCTGAGGCAG[A/G]AGAATCGCATGAACC | 8945 |
rs180806134 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101495335 | CTCCTTTCTAAGTAG[A/C/G]TATTTCTCTCCTGGC | 8945 |
rs180823158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439481 | CTATGAAGAAAAGAT[C/T]TAAAGTTGCAGTATC | 8945 |
rs180824024 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101506275 | CCTTTGAACTGAAGC[A/G]TGAAGCCATCAGCTC | 8945 |
rs180824887 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515049 | CAGCCTCCACCTCCC[A/G]GGTTCAAGCAATGCT | 8945 |
rs180826516 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101427912 | CTTAAGAAAATTTTA[A/G]TATCATTTACTTAAA | 8945 |
rs180831657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101483189 | ACGAAGGGTACCAAT[G/T]AGTCCTCTGTAGAAT | 8945 |
rs180833236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447652 | TGCTATTGATGATAG[C/T]TAATAACAGATATTA | 8945 |
rs180833403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472923 | CTGACTGTGATGGGC[C/G]TATATGTGTTGTTTT | 8945 |
rs180837734 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101401336 | TTTTAACAGTGTGGC[A/T]AAGAGTGTAAGTGAA | 8945 |
rs180862401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101462454 | GGAGGCTGAGGCAGG[C/T]GAATACCTGAAGTCG | 8945 |
rs180866714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537485 | GTGAGCCAAGATTGC[A/G]CCACCACACTCCAGC | 8945 |
rs180877728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101382424 | TTTTGAAGAGTTTGA[A/G]GTAGTTTTACAGAAT | 8945 |
rs180882975 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101419726 | GCGGTGGGAAACATC[G/T]GGGGGCATGTTAGAG | 8945 |
rs180979145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435023 | ATTTGTTCTATGTCA[A/G]GTTCAGCACACACAG | 8945 |
rs180982043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415907 | CAAATACTTTCCACT[A/T]TATTGCAGTTGCCTA | 8945 |
rs180985934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468478 | TAAAAACAACACGGA[A/G]TGATAGCAGATGCAG | 8945 |
rs180998525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101443697 | CTTCATTGTGAGATT[C/G]AGGTACTTAGATTTC | 8945 |
rs181008661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387572 | CACTCTGTTGCCCAG[A/G]CTGGAGTGCAATGGT | 8945 |
rs181018140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489902 | AATGGCCAAGAAACT[C/G]CCTTGTAATTTCCTA | 8945 |
rs181021714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423939 | TGCAGCTTTTAGAAT[C/G]CTTATTTTAGCCGGG | 8945 |
rs181026758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101360460 | CTCACTGCAACCTCC[A/G]CTTCCCAGGTTCAGG | 8945 |
rs181032550 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101377607 | CCTATTGTGGTTTCA[A/G]TTTGTATTTCCCTAA | 8945 |
rs181038593 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101404908 | GAGGCTGAGGCAGGA[A/G]AATGGGATGAACCCA | 8945 |
rs181136051 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | BTRC | GRCh38.p7 | 10:101520247 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8945 |
rs181143842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541986 | TTTCTAAGAGTTTGC[A/G]TATGTGATATTATGC | 8945 |
rs181152832 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101456937 | TTACAAAAATATTTT[A/G]ATATACTATAGTCCC | 8945 |
rs181167539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478054 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 8945 |
rs181172398 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101501123 | GCCTGAACCTGCGGG[G/T]CAGAGGTTGCAGTGA | 8945 |
rs181172665 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101552132 | CTCACTCCCAAGAGT[A/C]TGTTTCTGGCTTTTC | 8945 |
rs181173426 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101508827 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCAGGA | 8945 |
rs181181208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531563 | CTGTCTCTACTAAAA[A/G]TACAAAAATTAGCCA | 8945 |
rs181281791 | snp | A/T | 0.495634 | 0.0465208 | intron-variant | BTRC | GRCh38.p7 | 10:101505628 | CCGTCTCAAAAAAAT[A/T]AAAAAAAAAAAATAA | 8945 |
rs181286940 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101525847 | GGAAAAATTATTGAC[A/C]CTCATTTTACCCAAG | 8945 |
rs181289023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101496293 | GCACCAATTTTTATA[C/T]AGCAGTGAATAAAAG | 8945 |
rs181302813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546843 | TCAGAAATGAAAGAG[A/T]TCCCAGATCTTCACA | 8945 |
rs181305943 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101461301 | TTTTCTGTATTTTGC[C/T]TTGTAGATAGTGATT | 8945 |
rs181307453 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101482973 | TTTGTCCTTTAGTTC[A/G]AAGAGTGACTTTGGC | 8945 |
rs181316200 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101449038 | TAATTAGGAAAAAAA[A/G]TAATGATTAAACAAG | 8945 |
rs181332143 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101438524 | CATACATATATACTA[C/G]ATTGTGTCAAATTAG | 8945 |
rs181336755 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101419042 | TTGATACAGAGTCTC[A/G]CTCTGTCACCCAGGC | 8945 |
rs181351916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381609 | TTATCTTTTGACTTA[G/T]TTTTGAGAAATATAA | 8945 |
rs181379237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474690 | ACTTGATATCTCAAG[C/T]CAATAGACTGTGGCT | 8945 |
rs181411038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429936 | CTAATATTGTAATGT[G/T]TCTGTGAACTCCTCC | 8945 |
rs181426454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101401026 | CCCCATGATTCCCAG[A/G]CCTCAGCTGGTAGTG | 8945 |
rs181447791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395641 | TAAAATGATCATGCT[A/G]TGAAAGATCTTAGAT | 8945 |
rs181452068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359987 | TGGAGTAAAAATTCA[A/G]CTTTGAGTAGTTTTA | 8945 |
rs181452249 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101375843 | TTGGCATGTTCAGCA[A/G]GCATATCAGATGTTT | 8945 |
rs181452575 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BTRC | GRCh38.p7 | 10:101532809 | GTGTGCGCGCGCGCG[C/T]GCTTAGCTATACCTA | 8945 |
rs181453867 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101540312 | CATATGGTACAAGGT[G/T]TAGATCAAAGGGTTG | 8945 |
rs181468852 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101363519 | GCTGGAGTGCAGTAG[C/T]GCAATCTCAGCTCAC | 8945 |
rs181485059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101491856 | CTCTGTCTCGGAGAA[A/G]AGGCTTGGGACAGGG | 8945 |
rs181486652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101553151 | TTGCTCTGTTTTCAC[A/G]CAGGACCCATTAAAG | 8945 |
rs181490384 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101510597 | ATAATATAGACTTTT[A/T]AAAAATCTCTTCCTT | 8945 |
rs181508277 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366872 | TATTTATATATTAAT[A/G]TATATTTATATATAT | 8945 |
rs181581287 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101415705 | CGCCACCATGCCTGG[A/C]TAATTTTGTATTTTT | 8945 |
rs181585489 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101516066 | AGATTAAGCATTTCT[A/G]TTTATGTTATACTTT | 8945 |
rs181667655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101518528 | ATAGGACATAATCTC[C/T]GCCTTTTGATGGGAG | 8945 |
rs181691312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101477301 | CCACCAGGCCCCACC[A/G]TGATCTGTGTTTTAA | 8945 |
rs181701516 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418741 | GGTACATGTGCAGGA[C/T]GTGCAGGTTTGGTAC | 8945 |
rs181707704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400824 | ACTACTTCAACTTCT[A/G]TTTGCTCTTCTTGTT | 8945 |
rs181734687 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101380525 | CCCAGACGGTGGGGC[G/T]GCTGGGCAGAGGCAC | 8945 |
rs181735922 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101363390 | AAGGCACACTTTGGT[A/G]AATGCTAAAATAGAA | 8945 |
rs181766536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101539249 | TCATGTTGTTAGCCA[A/G]GGGCCCAGATTGATA | 8945 |
rs181772848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541705 | CATATGGTTTTTCAC[C/T]TTTATTCTGTTAATT | 8945 |
rs181785800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473849 | GCTATCCTCCTGCCT[C/T]GGCTTCCCAAAGTGC | 8945 |
rs181787665 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101456588 | AATATAATTACTTTC[C/T]TTTTTATTCGCCCAG | 8945 |
rs181788953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101495850 | GTTCACATCCACCCA[A/G]ATTTTAATAGGAAAA | 8945 |
rs181798313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515420 | GATCCAATTTCTGAA[A/T]ACAGTGTATCTCTCC | 8945 |
rs181811395 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101500181 | TATAGAGTGTACTTC[C/T]GCAAATCTAAATGGT | 8945 |
rs181825506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101429221 | CTGTAATAGCACTCA[A/G]GTTGATGGATAAAAT | 8945 |
rs181860766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101354908 | CTAGGGCTATAATGA[C/T]AGTCCCTGGGAGGGG | 8945 |
rs181866189 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101392044 | GAGTGCAGTGCCGCT[A/C]TCTCAGCTCACTGCA | 8945 |
rs181876805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490799 | TGTGGTGCCTCACAC[C/T]TGTAATCCCAGCACT | 8945 |
rs181899446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444234 | TTGTGATAGCTGTAC[A/G]TGTAGCTTAAAAAGA | 8945 |
rs181900311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424412 | GTATTACATGATTAT[A/G]GTATACTGCATTTCT | 8945 |
rs181906249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101499474 | TCAAAGTGATCTGCC[C/T]ACCTCGGCCTCCCAA | 8945 |
rs181908605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469171 | ACAGAACCTATCTTG[A/C]CTGTGGCTATTATAT | 8945 |
rs181910387 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101387879 | ATTTTTAGGAGAGAC[A/G]GGGCTTTGCCATGTT | 8945 |
rs181920552 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367018 | TATTTATATATATAT[A/T]TATATTTATATATTT | 8945 |
rs181923434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406486 | TATACTCTTTGTTCC[A/G]AGGTAAACTTTCATG | 8945 |
rs181934468 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101548955 | GTACTCAGGAGACTG[A/G]GGCAGGAGAATCGCT | 8945 |
rs182086177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101411980 | TCTAGTGTAGTTCAT[C/T]CCAGCAACTGAGATG | 8945 |
rs182091957 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101448159 | CCATTCTCTAGCATT[C/G]CAGTAACTTAAGACC | 8945 |
rs182112290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101371377 | GAGACGAAGTTCACC[A/G]TGTTGGCCAGGCTGG | 8945 |
rs182148042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532062 | CAGATTTATTATTTA[A/T]TTGAACAAATTATAG | 8945 |
rs182180102 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101516463 | AGTGGTTGAGAGTAA[A/C]CCATTTGTTAATGGA | 8945 |
rs182184328 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415536 | GTTATGTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs182193010 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101455863 | GATGATTCTAATGGC[C/T]GGGCATGGTGGCTTA | 8945 |
rs182196225 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375618 | AAACAGGTAGCAAAG[C/T]GTTGCTTCAAGCTTG | 8945 |
rs182204495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450380 | GTATTGTGATATTTT[C/T]GGTGACTTGAAAGTT | 8945 |
rs182250716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496506 | CTGTAACCTCGAGCT[C/T]CTGGCCTCAGGCAGT | 8945 |
rs182254544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101412592 | TAAACTTAATGTACT[A/G]GAAGTCCTCATATTA | 8945 |
rs182262390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101393183 | GATCCCTGGAGGGTG[A/G]TGTGCCCAGGGAGTC | 8945 |
rs182262802 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101431170 | CATCCTGCGCCTCCT[A/G]GGTTCAAGCAATTCT | 8945 |
rs182369475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544545 | CCCACATAGCTGACT[A/G]CAGGCTTGTGCCACC | 8945 |
rs182382214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367670 | GTTTTACTGTTATTG[A/G]TATGTAAGCTCATCT | 8945 |
rs182385784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101480183 | ATTGCCTTTATATCT[A/G]TTCATAGATTTGCTA | 8945 |
rs182394833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101503406 | TTATATAATAACTGC[A/G]TTTTGAAATCTGAAC | 8945 |
rs182398207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101522865 | TTAGTTCATGTTTAT[A/G]TACTTGGATTTGTAT | 8945 |
rs182401907 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352273 | AAACTTTTTATTAAC[A/T]GAAAGCCTATTATGT | 8945 |
rs182402283 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389103 | GAATGTTGCATAATT[A/G]TGATTTTTTGTGTGT | 8945 |
rs182409876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510069 | TACCTGGGAGGCGGA[A/G]GTTGCAGTGAGCCGA | 8945 |
rs182420756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460285 | AATAAATGTTGACCT[C/T]TCCCTTTCTTTGTTT | 8945 |
rs182421080 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101476767 | TTTTGTACTTGTTCT[A/G]TAAATCTAAAATTAT | 8945 |
rs182457142 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101433990 | TCTTTAATTCACCTA[A/C]AGACTATAATAAACC | 8945 |
rs182479534 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101359082 | GCACTAACATGATCT[C/T]CTGCGTGACTTCCCT | 8945 |
rs182479765 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101395025 | TTCCAACAGCAGTAG[C/T]GCCTAAATTCACGTT | 8945 |
rs182480811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486986 | ATACTAGGATTAGTA[A/T]TCAATCTTATTGAAA | 8945 |
rs182511440 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101403669 | GATCATGGCTCACTG[C/T]AGCCTCGACCTCTCA | 8945 |
rs182513570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101441791 | GAGGCTAAGGCACGC[A/G]AATCGCTTGAACCTG | 8945 |
rs182544058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463848 | ACTGTGACACATTCA[C/T]TTTTTAATTTACTAT | 8945 |
rs182544183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440964 | AATACCAAAAGGAGG[A/G]ATATTAAGAACTAGT | 8945 |
rs182567699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408939 | ATGAAAGCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 8945 |
rs182568382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373072 | TTTGTTAAATTATTC[C/T]TAGGAAGCAGATGTT | 8945 |
rs182645821 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101529202 | CATAAAAGGTTTTGA[C/T]TTAAAACATAAAGAC | 8945 |
rs182699799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101486040 | TAATTGCATTGTTAG[A/G]GCCAAGGAACAAGGC | 8945 |
rs182701452 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101506775 | ACTGAAGTTTACTTA[C/T]TTCCTAGCTATAGTG | 8945 |
rs182702232 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101412455 | TTCAGTGTCTTGAAA[C/T]ATATGTTTCACATAT | 8945 |
rs182704960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101549531 | CATCCTGGCTAACAC[A/G]ATGAAACCCCGTCTC | 8945 |
rs182732508 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101392693 | TTTTAGTAGAGACAG[C/G]GTTTCACCATAGTAG | 8945 |
rs182733945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464674 | TTTATCTCCATTCTC[C/T]TTGTGAAGAGCATGA | 8945 |
rs182735675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355364 | TTTGTGGGTGTGCTT[A/G]AACCCCTTGGAACAT | 8945 |
rs182742213 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101371743 | TACCTCTTCAAGTCC[A/G]TGAGAAGTTTTATTT | 8945 |
rs182746666 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540645 | CAACCAAAAAAGTCT[G/T]CTGGGAATGTTTTTT | 8945 |
rs182754462 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101507204 | TAACAGTACGTAGAA[A/G]GTTAACTGCCTGGAG | 8945 |
rs182764669 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101421769 | GAATGATGGTTTCCA[G/T]CTTCATCCATGTCCC | 8945 |
rs182783796 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553670 | GCTTAGGAGGAGACA[C/G]AGTTCCCTCTGTATA | 8945 |
rs182819408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470766 | ACTTAATTCTATGAT[A/C]CATCTCAAATTAATT | 8945 |
rs182827145 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101470169 | TTTGCCTTTTTATTA[C/T]TGAGTTGTAGACTCA | 8945 |
rs182840515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512336 | GCCTTTCTCAAAGCC[A/G]AATGGAATCCTTAGA | 8945 |
rs182850808 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101355728 | CAAAATTGAATTTTA[G/T]ACTTTAAACTGCCCC | 8945 |
rs182853210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379077 | TAAAAACAATTTAAA[A/C]GCTAGTCAAATTAAT | 8945 |
rs182861815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417217 | AATCTCAGTCAATGT[C/T]CTTTATATAATAGAA | 8945 |
rs182865273 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101399147 | TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC | 8945 |
rs182867898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425105 | TGGCTTCTAGCTGCA[C/T]CCATGTTCTGCAGAG | 8945 |
rs182875177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362042 | CTCAGCTCACTGCAA[C/T]CCCCGACTCCCTGGT | 8945 |
rs182910649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550325 | AGTCTCACTCTGTTG[A/C]CCAGGCTGGAGTGCA | 8945 |
rs182973500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101383784 | GTTGGGAAAATTTTG[A/G]CAATTGGCTAAATTA | 8945 |
rs182988745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101402094 | TTGGGTCATTCTAGT[C/T]TCTCTGGTAAATTCA | 8945 |
rs183002192 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101365213 | TGAGTAGCTGGGATT[A/C]CAGGCATGCACCACC | 8945 |
rs183010089 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101421295 | TCCTGTGCCCCTAAA[C/T]CATTTTGGCTTCCCA | 8945 |
rs183053015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384049 | ATATTTGTAGCATTT[A/T]TATTTGTCGAATTTT | 8945 |
rs183101105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534081 | CACACAAAATTCTCA[A/G]GCTATCCAAGGGCCC | 8945 |
rs183132564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440483 | CTCAATACTTTGGGA[A/G]GCTGAGGTGGGTGGA | 8945 |
rs183137681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493184 | ATTTTCACTTGCACG[A/G]GTAGGTTCTCAAAAT | 8945 |
rs183139075 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101420106 | TACCTAGGAATTTCT[C/T]GGTGTAATACATTGT | 8945 |
rs183143761 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101463052 | TTTGTATTTTGGGGT[G/T]TTTTTTTTTTTGAGA | 8945 |
rs183162387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445176 | CTCTCTGGTAAGATC[C/T]TTCTGATTTCTTAGA | 8945 |
rs183201588 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101541216 | ATTCAGTCTTTCACC[A/G]TTTCACATATGTGTA | 8945 |
rs183232930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497179 | GTAGTTCCCATTATA[C/G]CGGATTGTTTTCTTT | 8945 |
rs183246837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516929 | AAGACAAAGGGTGCA[C/T]TTTAAAAGGCAAATA | 8945 |
rs183252676 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101540721 | AGACTGGTCTCAAAC[C/T]CCTGGCCTCAAATAG | 8945 |
rs183309218 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101365568 | GCAACCTCTGCCTTC[C/T]GGGTTCAAGCAATTC | 8945 |
rs183310678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101403259 | AGCAAGAAGGGAGAG[C/T]ATTTTAAGGGTACAG | 8945 |
rs183344771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522275 | TGGATCTCCTGACCT[C/T]GTGGTCCACCTGCCT | 8945 |
rs183371324 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101409076 | AAAAAACAAAAAAAG[A/C]CACACAAAACATTGA | 8945 |
rs183373472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101479790 | TTTAAATACAGTTAC[A/G]TATAGAGTACATCAC | 8945 |
rs183379438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389405 | CTCCCCTTTAAATCT[A/G]GTCTGTCTCCACACA | 8945 |
rs183390419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425963 | TAAATTTTAAAGGGC[A/G]TTATTTATTAAATGT | 8945 |
rs183407696 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101444888 | GGTGTGGAGTAGTCT[A/C]ACCACCCTCCCTCAT | 8945 |
rs183423562 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407238 | CTGTAGTCCCATCTA[C/T]TTGGAAGGCTGAGGC | 8945 |
rs183532203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101512526 | GTCATTTCACCATAA[A/T]GTTCAGTCAGTCCAC | 8945 |
rs183538041 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | BTRC | GRCh38.p7 | 10:101356084 | AGTGCAGTGGTGCAG[A/C]CTCCGCCTCCTGGGT | 8945 |
rs183544943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432587 | GGGAATTGTAGTGCC[G/T]AAAAGGCTGCTCCTA | 8945 |
rs183549669 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101415183 | CCATTTTTTATCTTT[A/T]TGTCTTTTTTTTTGA | 8945 |
rs183554218 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446031 | CTGGGTCACTGCTTT[G/T]AATGTCTTATTGGAT | 8945 |
rs183554299 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101471525 | GTTTCATGTGAGGTA[C/T]TGGTTTGCAGTTTTC | 8945 |
rs183560369 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101454723 | GGAGTTGGAGGTTAC[A/G]AGGAGCTATGATCAT | 8945 |
rs183568777 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101543130 | TGATCCACACACCTC[A/G]GCCTCCCAAAGTGTT | 8945 |
rs183574037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502066 | TAAATAACCTCCAAA[G/T]TTACAGGGTAGTAGA | 8945 |
rs183611052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424775 | TATATTCTTCTTGAA[A/G]CACTGGAGGCCCTTC | 8945 |
rs183661778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541420 | ACGTGCCACCATGCC[C/T]GGCTGATTTTTTGTA | 8945 |
rs183677742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101388158 | TTTTAGCTAGGAAAG[A/G]TGGCTTTCTTTTGTT | 8945 |
rs183688181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476152 | AAATATCAGACAAAC[C/T]CAACTTGAGGCACAG | 8945 |
rs183689626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499123 | GGAAGTAGGTGGTAT[C/T]AGTTTTGTTTACAGG | 8945 |
rs183703212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506666 | AGATTCAAAATTGAC[C/T]GAAAGGAAATCTTTC | 8945 |
rs183703613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517798 | ATCAGCAAATTCAGT[A/G]GGATCTGTCTTCAGA | 8945 |
rs183704958 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101475585 | ACTTTATAATATCGA[C/T]GGGGAGTTATATATC | 8945 |
rs183720041 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101393471 | ATGAGGCCCGAGGCT[C/G]TCTTTTAAGGGGTGT | 8945 |
rs183744498 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101431609 | CAAATTAGTTTTTAT[A/G]TTAATATTTGCCTGC | 8945 |
rs183747848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101543933 | TTGTTTGTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 8945 |
rs183755200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384422 | GCAGGTAGATACTTA[C/T]GTTATGTAGCTAAAC | 8945 |
rs183757247 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101366038 | TTTTCCTTTCAGTTC[A/C]TGTTAATTTCTAAAT | 8945 |
rs183780662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373766 | ACTAAAAAATACAAA[A/G]AATTAGCCAGGCATG | 8945 |
rs183829672 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101427262 | AGCTGGGACTATAGG[C/T]GTGCACCACCATACC | 8945 |
rs183847767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101391158 | TGTGTGGTAACTACC[A/G]CTCCTGCTGTGATTC | 8945 |
rs183851214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437416 | CCATGTGTGCCTGTG[C/T]GTGCACACACACACA | 8945 |
rs183856324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101370711 | GTAGCTGGGACTACA[A/G]GCATGTACCACCAAA | 8945 |
rs183864636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410340 | AGAGTACCCTGGCTG[C/T]GCAGGGTGGCTCACA | 8945 |
rs183873925 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353780 | GCCGCTACTGGCGTC[G/T]CTCGGTAACCACGGA | 8945 |
rs183887628 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101458847 | ATCTGCTGGATTTCT[C/T]CACTATGAGGTTACT | 8945 |
rs183909241 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101484934 | TAAGAGAAGCCAGGA[A/C]CCCTCTTATAGACAA | 8945 |
rs183912927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452401 | CCTATCCATCTGCCA[A/G]CCAGATTGGAATTCT | 8945 |
rs183922964 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101378001 | GAAATAAGTGAGAAA[C/T]GCTTATGGACACTGT | 8945 |
rs183925957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526919 | CCAAAGCATCATATA[C/G]TTAGCAGTCTAAGAG | 8945 |
rs183929289 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352778 | CTGGAGTGCAGTAGC[A/G]TGATCTCGGCTCACT | 8945 |
rs183931070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417039 | AACCACTTGAGAATA[A/G]GGTTCTGACATGATG | 8945 |
rs183988130 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101393719 | AGTGGAAAAACACGA[A/G]GTTGGAAAGAGTCTT | 8945 |
rs183992951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101374123 | TCCAGTTCTAGATCC[C/T]GGAGGAATCGCCACA | 8945 |
rs183996775 | snp | C/T | 0.0150961 | 0.0855578 | intron-variant | BTRC | GRCh38.p7 | 10:101414661 | GCTCCCAAAGACCTT[C/T]CAGTGCCATAAGCTA | 8945 |
rs184019300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357533 | TCCTTTTAATCAAAC[A/G]GGCATTTTTATTACT | 8945 |
rs184060104 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436321 | CTTTAGATATTGAAA[A/G]AGAAGAGAAATGAAA | 8945 |
rs184063597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101535204 | TTAGCCTCTGTTACC[A/G]TGAATTTAAATTGTC | 8945 |
rs184069956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101479176 | ATACTTGTTCATGGG[C/T]ACATCAGTGGCTTTT | 8945 |
rs184071756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101398366 | GGAGTACAGTGGCGC[A/G]ATCTCAGCTCGCTGC | 8945 |
rs184080602 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101501277 | TCTATTTTTAAATTT[A/T]TGTACGCAATTTTAT | 8945 |
rs184096829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101368692 | GTATGGGAGTCCCAG[C/T]TGCTGAACATTCTTG | 8945 |
rs184103393 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101360998 | TTTTGTAGAGATGGG[C/G]TCTTGCTGTGTTGCC | 8945 |
rs184149823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101432252 | CCTACCTCAAACTTC[C/T]GGGTAGCTGAGACTA | 8945 |
rs184229997 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554381 | GATCAAGGTAGCTTA[A/C]GAGAGATGGTCAGGA | 8945 |
rs184250500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101375212 | CTTTTGTGCTGTTTT[C/T]GTGATAGAGTTCTCA | 8945 |
rs184269663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551701 | GTTTCTGCATCTCTC[C/T]TTGCAGTGTTCCGCT | 8945 |
rs184288511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508635 | AGAACTAAAAGTAGG[C/G]TGGGCGTGGTGGCTC | 8945 |
rs184295153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101531158 | CCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 8945 |
rs184313257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101467709 | GGTAAAAAAAAAATT[A/G]CCTGAGATGTTTATT | 8945 |
rs184325422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489688 | TGACTCTTCTACTCT[A/G]TACCAAGTTTCTATG | 8945 |
rs184415577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101531699 | GCACTCCCTCCTGAA[C/T]GACAGAGCGAGACTC | 8945 |
rs184416105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101394132 | ATTATGGAGCTAGAG[A/G]TGGAGATCTATGACT | 8945 |
rs184433355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358951 | GACTTGCTACCGTAG[A/G]TGCTATGCTAGTTGG | 8945 |
rs184445958 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101400869 | TCTTTTTTCATTTTC[C/T]TCTGCCTTTCTTTCC | 8945 |
rs184452226 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438230 | AGGAGATTGAGACCA[C/T]CCTGGCTAATGCGGT | 8945 |
rs184457865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494248 | TGTTGCACATGCAGG[A/G]AAGATCCAGGACTGG | 8945 |
rs184457880 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418754 | GATGTGCAGGTTTGG[A/T]ACGTAGGTAAACATG | 8945 |
rs184479840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101381166 | CCAACACTTGTAGCT[C/T]AGTATATACCGTGCA | 8945 |
rs184498899 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101552178 | TATTTTATTTTATTT[C/T]ATTTTATTTTATTTT | 8945 |
rs184536639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508879 | AGATTGTGCCACTGC[A/G]CTCCAGTCTGGGCAA | 8945 |
rs184559056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515025 | CAGTGGCACGATCTC[A/G]GCTCACTGCAGCCTC | 8945 |
rs184582849 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556437 | TTGGTACTGTTGACC[C/T]TCTCAGCATCTCCCT | 8945 |
rs184596822 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101472836 | TTTATATCGTTACTC[A/C]TAGATACCTAACATC | 8945 |
rs184608173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460995 | GCAACCTCGGCCTCC[A/T]GGGTTCAGGCGATTC | 8945 |
rs184615621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514056 | TTCATATGCTTATTG[G/T]CATCTGTGGATCTTT | 8945 |
rs184624198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535996 | TGTTTGTTATATCTA[A/T]GGAAATTATTCCTAG | 8945 |
rs184637718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362500 | TCCCGGGTTCAAGCT[A/G]TTCTCCTGCCTCAGC | 8945 |
rs184639698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101399578 | ACTGGAATGTCACAA[C/T]GCAAGGATGTGAATC | 8945 |
rs184681817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101495231 | GTTTGGTAACATGTT[A/G]CTTTGTTGGTGGAAC | 8945 |
rs184691895 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101541556 | TGAACCACCGCGCCC[A/G]GCCTAGGGTTTTTCA | 8945 |
rs184703635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101537070 | GGGTTTTTTATCTCT[C/T]TGAGTAATTTTTAAG | 8945 |
rs184711999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447539 | TCTGTACTGTAAGAA[A/C]AACTACTATGATATT | 8945 |
rs184722257 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556838 | AAATATGTGCTTTCC[A/G]ACCAGCACAGCTGGC | 8945 |
rs184737106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417289 | TACCTCTTTAGTCTC[A/G]TTTACTCTGGAACAG | 8945 |
rs184754686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466870 | TGAAAAAATTCCTGC[A/G]TTCTAAACATTGCCT | 8945 |
rs184756732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487794 | GTGGAAACAGAGGGA[A/C]TGATGAAGGGAGCAC | 8945 |
rs184759038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379274 | CTCTTACCTGACACA[C/T]ATGCACCTCATCAAT | 8945 |
rs184766420 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404006 | TGTGTGTGTGTGTAT[A/G]TATATATATATATAT | 8945 |
rs184776447 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | BTRC | GRCh38.p7 | 10:101442154 | TATTTTAAACCTAGC[C/T]CCAGTTCCTGAAGAT | 8945 |
rs184780192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423089 | ATTTTCCAGTTTTTC[A/G]TAAAAATAGAGATGG | 8945 |
rs184796764 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101385738 | CTTCCCAGACACACA[A/C]ACACACATATGTTTT | 8945 |
rs184819421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545531 | AGGTTAAATGAAGTC[A/G]TTGGAGTAGGCCCTA | 8945 |
rs184819600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495572 | CATATGGGAACAATT[A/G]TCTGTATGTGGCCAT | 8945 |
rs184825420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515077 | GCTCCTGCCTCAGCC[C/T]TCAGGGTAGCTGGGA | 8945 |
rs184833475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101428028 | ATTTTCTCCATTCTC[C/T]TTCTGTTGCCTTCTC | 8945 |
rs184850875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473306 | TTTGATTTTTTTGAG[A/C]TAGGGTCTCACTCTG | 8945 |
rs184851959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448031 | TGATTCTTTAAATCG[A/G]AGATAGTTACGGTGT | 8945 |
rs184904255 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366879 | ATATTAATATATATT[A/T]ATATATATTTATATA | 8945 |
rs184928530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101497705 | AGTGAGACCCTGTCT[A/G]TCAGTCAATCAACCC | 8945 |
rs184933539 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101363248 | CTTGCTCAAAGTCAT[C/G]CTAGCAGGTATCCTG | 8945 |
rs184935895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379659 | ATTAAAATGAGAAAT[A/C]TTTGTTTAAAGTGGC | 8945 |
rs184960096 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | BTRC | GRCh38.p7 | 10:101387173 | CATATAGCTTTTTTT[G/T]GGGCAAATCTTTTCT | 8945 |
rs184964449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423436 | AAGTCTGTGACTGAG[C/T]TTTTCTAAATATTTG | 8945 |
rs184966556 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101453100 | AAAATAATAATTTCT[A/G]TTTTTGTAAATTGTA | 8945 |
rs184987659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387639 | TCAAGCGATTCTCCT[A/G]CCTCACCTTCCCGAG | 8945 |
rs185002337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101405051 | TTGGGTTATATCCAC[C/G]CATGTGCAGCTTGGG | 8945 |
rs185020506 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366902 | TTTATATATATTTAT[A/G]TATATTAATATATAT | 8945 |
rs185043772 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101443343 | AAATGTAGTCCTGCG[C/T]AACATTAAAAGCAAA | 8945 |
rs185046224 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101517456 | TAAATAAAAGAAAAT[A/G]AGGCAAGCCTGAGCC | 8945 |
rs185060726 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101404453 | CCAAGTAATTTTTGC[A/G]TTATATCCTTGGCTT | 8945 |
rs185079691 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101475869 | GATGCTAAAATTAGC[A/T]AGCTGAGATGCAAGT | 8945 |
rs185082945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446951 | GATTGATTTTTTTAT[A/G]TGTGTCCTCTTGAAA | 8945 |
rs185114200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409767 | TGACTAAAAATGTCA[C/T]TGTGCAGTGCGTGAG | 8945 |
rs185134473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369275 | CAGGCTCTCGAGTAC[A/G]CTGGTGTGATCATAG | 8945 |
rs185200298 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101471936 | TCATATTGGGCTACT[C/G]AAAGCCTCTTTCGGC | 8945 |
rs185205451 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101540663 | GGGAATGTTTTTTAA[C/T]TTTTTAATAAATAAA | 8945 |
rs185219128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390746 | CACAACCACTTTTAT[G/T]TAATTTTGTTTGTCT | 8945 |
rs185227358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101426062 | ACTTAATAAGGATAG[C/T]AACCAAAATGACAGT | 8945 |
rs185228166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524740 | CTGTATTTAACATGA[A/G]GAACTAATTATTATA | 8945 |
rs185258032 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353482 | ATTCGGCCCTGACTT[A/G]CTGTGGGGGAGAAAA | 8945 |
rs185340089 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101501181 | CAACAGAGTGAGACT[G/T]CGTCTCAAAAAAAAA | 8945 |
rs185345743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520328 | AAAATGCTGGGATTA[C/T]AGGTATAAGCTACTG | 8945 |
rs185349642 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546028 | CCACTGTTATAGTTG[A/G/T]AGACTTCAGCACCCC | 8945 |
rs185356495 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101542729 | GGCGTGCGCCACCAC[A/G]TCCAGCTAATTTTTT | 8945 |
rs185369110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507715 | AGGCTGTGTCCTGAA[A/G]TGATTAGCACAGTGA | 8945 |
rs185373778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457039 | ATGTTTTTTCCTATG[A/G]ACACATACCTATGAT | 8945 |
rs185375344 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | BTRC | GRCh38.p7 | 10:101478292 | GGCAGCAGAGCAAGA[C/T]TCCATCTCAAAAAAA | 8945 |
rs185376729 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101477017 | AGTCTTGCTCTGTCA[C/G]CCACGCTGGAGTGCC | 8945 |
rs185388853 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101518240 | AATTGGCCTCCTTCT[A/G]TTTATGTCCCATATA | 8945 |
rs185405174 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101435666 | AAACAGTTTTGTATA[A/C]GTCTTTTTTTTGGCA | 8945 |
rs185410074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434272 | CAGTTTCTTGAAGAT[C/T]AGTTGCAGTATGGTA | 8945 |
rs185425575 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101395298 | AGTCTAGCCAGGCAG[C/G]CTAGGATAGGAAATT | 8945 |
rs185497240 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101529849 | AGGGAGGAGTGGATG[A/T]CTGGCCCAGAGAAAA | 8945 |
rs185506049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101499506 | GTGCTAGGATTACAG[A/G]TATGAGCCACCATGC | 8945 |
rs185507943 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101412471 | ATATGTTTCACATAT[G/T]TTGTTCAGTTTCTTG | 8945 |
rs185516565 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101461605 | CTGTGCCAACCAAAC[A/G]TCTACTATAATCGAG | 8945 |
rs185523234 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101415567 | TTATTTTGAGACAGA[A/G]TTTCACTCTTGTTGC | 8945 |
rs185528985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101430545 | CCCATACTTTACTTA[C/T]ATTCATCTTTTCTCC | 8945 |
rs185529170 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483076 | GACATTAATACTATT[G/T]ATTTCCCTAAAAGCA | 8945 |
rs185533669 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101456040 | GCTGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 8945 |
rs185547121 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392775 | GCGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 8945 |
rs185551387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101355410 | TATCACGCTTTTCTT[C/T]TTGCTGTGCTTATCT | 8945 |
rs185553439 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101372480 | GGCTGGTCTCGAACT[C/G]CCTGACCTCGTGATC | 8945 |
rs185561982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375619 | AACAGGTAGCAAAGC[A/G]TTGCTTCAAGCTTGA | 8945 |
rs185579259 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101492022 | GGTTAGAAATGCTTG[A/T]CAGTTAAGGGTGGCA | 8945 |
rs185660224 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101546909 | AAACTAAGCCTAGGC[A/C]GATCCACTGGTGAAT | 8945 |
rs185679098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101505874 | CAGATTTGATCCTTT[C/T]TGAAGATGAATTTGG | 8945 |
rs185685197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449105 | TCTTAATCTAGCCCA[A/G]TCTAGCTTTCAGAAA | 8945 |
rs185691203 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101525908 | TAGGGACAATGATGT[A/G]CCTTCATAGCAGAAC | 8945 |
rs185700302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400356 | TCTACACAAAAGTTA[A/C]ATTAAGGAGTACCCA | 8945 |
rs185710093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460403 | GGTAGATGATCTCCA[C/T]TCCTTTTTTTCCAAA | 8945 |
rs185720514 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101504264 | TGGTTTTAAAAAATA[A/G]TTTTTTATCTCCTCT | 8945 |
rs185728843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418464 | AATAGTTATTACAAT[A/T]TTAAATTTTTCAAAA | 8945 |
rs185730288 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553422 | TCCTTTCACCTCTGC[A/T]CCTAGTTTTTTCCCA | 8945 |
rs185746754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533336 | CTTTTCTTATCCTTA[C/T]GGTAAACTTTGCATT | 8945 |
rs185813725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523534 | TTACCTTGTTAGGGG[A/T]GGGGTTTTGGTTGTT | 8945 |
rs185826223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101456793 | CATTCTGCCCTTTCA[A/G]TTCTAAGCTAGTAAG | 8945 |
rs185846938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481273 | ATCCTGCTTTTGTGC[A/G]TGGAAACAGGGATAC | 8945 |
rs185850582 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101415736 | AGTAGAGACAGGGTT[C/T]CATCATGTTGGCCAG | 8945 |
rs185858401 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101395989 | TTTGTATTTTTGTTT[A/T]TTGCCTCAGCTTTTC | 8945 |
rs185860333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434455 | AAATGGATCATAGAC[C/T]TAAATCGGAGTTAAC | 8945 |
rs185870189 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377797 | GTTTTTCAGTGAAGT[C/T]TGAGGTACTCTGAAG | 8945 |
rs185883971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437883 | ATTGTCCCTTACCCA[C/G]TCTCTGCCTTTGTCT | 8945 |
rs185890366 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101376600 | CAATAAAACTGGTAG[A/T]TTTTCCTAGTACTAT | 8945 |
rs185892438 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101360046 | AAACTTTCAAAAGAG[A/C]TCTCTTTTTTTTAAA | 8945 |
rs185893124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485027 | TTTAAGAAAAATACA[A/G]ACATGGGGCACCAAA | 8945 |
rs185897474 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101539562 | GCTGAGTAGTATTCT[A/G]TTGTATGGTTATACC | 8945 |
rs185902027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506714 | TCAGTTGACTAACCC[C/T]AGGTATGCAAGGTGG | 8945 |
rs185921277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440614 | GTGGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 8945 |
rs185921583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420149 | TACAACAACATCCTC[A/G]ATTCTAGTTCAGCAA | 8945 |
rs185935449 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515592 | TCTCAGCTCACTGCA[A/G]TCTCCACCTCCCGGG | 8945 |
rs185937861 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101463371 | TTTTAGTAGAGACAG[G/T]GTTTCACCATGTTGG | 8945 |
rs185984812 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360726 | CTTGAACTCAGGCTA[G/T]GGTTAAGTGATCTTT | 8945 |
rs186001455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424166 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8945 |
rs186009266 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490331 | GAGGAGAGAGAATAC[A/G]TTAAAATGTATTCAG | 8945 |
rs186010930 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101355253 | TAGGAGATAAAAAGG[A/G]TGGAGGTTGGTAGAG | 8945 |
rs186031694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444103 | AAATGGTATACTTAT[A/G]TTCATATCAGATATA | 8945 |
rs186048187 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101416028 | GATTTGTGTAAGTAC[A/C]CTGTGATCACACAGC | 8945 |
rs186073323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424490 | CATGGCTTAAGGATA[C/T]GTAAACTCTCAGTAC | 8945 |
rs186081324 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444380 | GCTATAACTGAGAAA[G/T]AGTCTATTGCATACA | 8945 |
rs186083118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469244 | TATTGAATGGAAAAT[A/G]TTGAATGTTTTAGCC | 8945 |
rs186087037 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BTRC | GRCh38.p7 | 10:101388044 | AACAAATATCTAAAG[A/G]CAAAAATATACTAAA | 8945 |
rs186103193 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406878 | CAGCTTCTTTAAGCT[C/T]TTTACTTTTAATTTA | 8945 |
rs186160305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438929 | TAGTCCTGGAAATGT[A/G]CCTATGGACTATTTA | 8945 |
rs186164062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101397095 | AGGCATGAGCCACTG[C/T]GCCCAGCCTGTCCAA | 8945 |
rs186172421 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101468843 | TCAATCCCTTTTAGT[A/G]TGTTATATGTTTCAC | 8945 |
rs186206598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363783 | AGATATCTCTCTGAG[G/T]TAGGCAGTCAAGCGG | 8945 |
rs186234667 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490879 | GCCTGGCCAACAGGA[A/T]GAAACTTTGTCTCTA | 8945 |
rs186246624 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101510240 | TTGGCCGGGTGCAGT[G/T]GCTCACGCCTGTAAT | 8945 |
rs186254329 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101532205 | ATCCCATAGAGTAAA[A/G]CATTGAGCCATTGAT | 8945 |
rs186307607 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101516195 | AGAGTGTTGATTGAC[A/G]GAACACTTGACTGTA | 8945 |
rs186327569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101359501 | GGCACAATTTCGGTT[C/T]ACTGCAACCTCCGCC | 8945 |
rs186335218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474712 | ACTGTGGCTTTCAGA[C/T]TGAATTCTAGTCACC | 8945 |
rs186339718 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101381615 | TTTGACTTATTTTTG[A/G]GAAATATAATTTTGA | 8945 |
rs186351140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101419259 | CAGGCGATCCACCCA[C/T]GTCGGCCTCCCAAAG | 8945 |
rs186420787 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101383165 | ACCTCCCAGGCTCAA[C/G]TGATCCTCCCACCTC | 8945 |
rs186434217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401484 | TTTTGGTATAGAAAA[C/G]ATGTAGCATCAAAGC | 8945 |
rs186442385 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101365209 | TTCCTGAGTAGCTGG[A/G]ATTACAGGCATGCAC | 8945 |
rs186449051 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101411639 | TTTTTATTTCATTCT[G/T]TTTTTATACCCTACA | 8945 |
rs186473165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101470608 | GTGCTGGGATTACAG[A/G]CGCGAGCCACCGCGC | 8945 |
rs186478981 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101541809 | TATAATTCTTTTTAT[A/G]TGTTGTTGGATTCAC | 8945 |
rs186490365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424883 | ATGCTGAGGTTTGGA[A/G]TCTGAGTGAATCTCA | 8945 |
rs186490939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540574 | GCTTTGTCTTTTTCA[A/G]AGTTTTTTGGGGCCT | 8945 |
rs186502090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101500406 | GTTATTGACTAAAAT[A/G]TCATCACATGGTGCA | 8945 |
rs186515332 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BTRC | GRCh38.p7 | 10:101388601 | TTCAAGTGATCCTCC[C/T]ACCTCAGCTTCCCAA | 8945 |
rs186538376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496330 | CATTCCTTTTTCTCA[C/G]CAACCAACACTTGGT | 8945 |
rs186649832 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101371528 | TACCTCATTTAAGTA[A/G]AATCATACAGTGTTT | 8945 |
rs186657631 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481001 | CTAGCTCAATGCAGC[C/G]TTTACCTCCAGGGCT | 8945 |
rs186666202 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101518791 | TCGCTGTCTAGTCCT[C/T]ATTTCCTTCATGTCT | 8945 |
rs186666664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101504142 | TCTGGTAATCTTAAC[A/G]TAATTTGACATCTAG | 8945 |
rs186671771 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523106 | CTACTTGGGAGACTG[A/G]GGCAGGAGAATCGCT | 8945 |
rs186675087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516581 | AACAGTTGATAAATA[C/T]GTGAAATCTCAGTTT | 8945 |
rs186695085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460286 | ATAAATGTTGACCTT[C/T]CCCTTTCTTTGTTTG | 8945 |
rs186704330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477796 | CTGGAACTACAGGCA[C/T]CCACCACCATGCCTG | 8945 |
rs186705715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407444 | CTTTGGAAACAGTCT[C/T]GCTTTGTTGCCCAGG | 8945 |
rs186716366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101445049 | TTCTGGTAGAAACTC[A/G]ATATGTTAGGGTTTA | 8945 |
rs186813825 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101544719 | CCTGGCTCTGAAAAA[A/G]TTTTCGTTTTGCCTT | 8945 |
rs186821175 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101496173 | GGTTTCTTTCAGATT[C/T]TCATAACTACAAAAA | 8945 |
rs186847956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412267 | TCACTAATTCTTTTT[A/G]GCCTTCATGTATTTT | 8945 |
rs186850212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408954 | TTTGGGAGGCTGAGG[A/C]AGGGCAATCGCTTGA | 8945 |
rs186856529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448878 | TATCTATGCTGAGAC[A/G]TGTTTTTCAGCCTTG | 8945 |
rs186860935 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101425124 | TGTTCTGCAGAGGAC[A/G]TGATTTCATTATTTT | 8945 |
rs186879691 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352473 | TTGGGGTACAAGTGG[C/T]TTTTGGTTATATAGA | 8945 |
rs186882288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392125 | GCTGGGATTACTGGC[A/G]TGCGCCACCACGCCC | 8945 |
rs186884542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389160 | TTTTGCTGATCTTCC[A/C]ATACTAATAAATGGT | 8945 |
rs186889842 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101367991 | GTCACAGGGTATGAA[A/T]ATGTTTAGCTTTATG | 8945 |
rs186938626 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101528095 | GAAAAAAAGAATCTC[A/G]TCTCCAAATAACTCC | 8945 |
rs186972820 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101432253 | CTACCTCAAACTTCC[A/G]GGTAGCTGAGACTAC | 8945 |
rs186973072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486388 | GCGGAGTGCAGTATG[G/T]TGCAGTCTTTTAGTG | 8945 |
rs186975612 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101453862 | TAAAGGGGCAGATAA[G/T]AAACATTTGAGGCTT | 8945 |
rs186978017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507100 | GTTTCCTTGCATTGC[C/T]CTTCTCCCTGTTTTT | 8945 |
rs187012493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414836 | AAGATGTAAGGAAAA[A/G]TATTTTTGTACTGCT | 8945 |
rs187014993 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393908 | ATTGTGGAAAAGCAG[C/T]TGAATGAGAAAACTA | 8945 |
rs187015336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101549141 | AACAAATTAATAACA[A/G]TAACAGCATTGGGCC | 8945 |
rs187020729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474266 | TGGCTGATCACTATG[A/T]CCTTGTGGAGGCTTG | 8945 |
rs187047395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429321 | TTACAAAGCTGTAGC[C/T]GCAATAATACTAATG | 8945 |
rs187103372 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101437019 | ACAAAACAATACCAT[A/G]AGGAAAATTATCCTG | 8945 |
rs187112159 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459993 | GCAAAAAGTAATTAG[G/T]CTCCAAGTTATATGA | 8945 |
rs187143053 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101379084 | AATTTAAAAGCTAGT[A/C/T]AAATTAATTGAGAAG | 8945 |
rs187151175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417246 | AATAAATATCTAGTT[C/T]AGGATCACATGATAC | 8945 |
rs187152872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399531 | AAAGACTGTCAGTAC[C/T]TATATTCCGTGTGCC | 8945 |
rs187155139 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101521127 | AATGTTAAAAATTAG[C/T]AGGACATGATAGTGT | 8945 |
rs187164346 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | BTRC | GRCh38.p7 | 10:101362252 | GTGAGCCACCGTGCC[C/T]GGCCTTGAGTTGGAA | 8945 |
rs187176155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101553070 | CCTTTTCCCCATTGG[C/T]AGCTAAGTGAATGTT | 8945 |
rs187181852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479257 | ATAAGTCTTAACTTA[C/T]AGATAAAATCTATTT | 8945 |
rs187189716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101354670 | GCGGGATAGAGTGAA[A/G]ACAGATACGGTGGGT | 8945 |
rs187269511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479830 | AGGACTGTGAAATAT[G/T]CTATAGACAACCCAA | 8945 |
rs187275586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101503015 | TATTTTAATCTTAAC[A/G]TTAGCCCTTCTAGCT | 8945 |
rs187320244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506392 | CTTTCTCTGTCCTCC[C/G]AAAATTTAGCTCATG | 8945 |
rs187332524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548451 | ATCTTATAATGTTGA[C/G]TAAAAGAAGCCAGGC | 8945 |
rs187341519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101501548 | GAATGGTTTGTTTCC[A/C]GAGCATCAAAGTTCA | 8945 |
rs187357889 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101462513 | GAGAAACCCAGTCTC[C/T]ACTAAAAATACAAAA | 8945 |
rs187363430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543135 | CACACACCTCGGCCT[C/T]CCAAAGTGTTGGGAT | 8945 |
rs187374707 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556438 | TGGTACTGTTGACCT[A/T]CTCAGCATCTCCCTT | 8945 |
rs187387480 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101419771 | TTATCCATTATTATC[A/G]TTATTTAGTTTGATA | 8945 |
rs187422404 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101391827 | TAAGTAAATATATAT[A/G]TGTAAATTGTGTCCA | 8945 |
rs187431076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101373867 | AGTTTGCAATGAGCC[A/G]AGATCGTGCCACTGC | 8945 |
rs187442904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383913 | AGATGGAGTCTTGCT[A/G]TGTTGCCCAGGCTGG | 8945 |
rs187443283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101356425 | CTTCAGCCTAGTAAC[A/G]TTCTCAGCTACTTAA | 8945 |
rs187460041 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101402404 | AGTTTATCAGTGTTG[C/T]ATTTGACTAATTGCC | 8945 |
rs187500979 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101465317 | TTTTTAACTAATATT[A/G]TAGTTGACATATATT | 8945 |
rs187508121 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101550331 | ACTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGAG | 8945 |
rs187514322 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101507357 | TATATTTATCTTACA[A/G]TTTGCCAGGGGGTGA | 8945 |
rs187530076 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540783 | ATTATAGGCCTGAGC[C/T]ACTCCATCTGCTGGG | 8945 |
rs187547279 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101378585 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGTGCAC | 8945 |
rs187562632 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | BTRC | GRCh38.p7 | 10:101361365 | ACCGCCTCAGCCTCC[C/T]TAAGTGCTGGGATTA | 8945 |
rs187591634 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101526694 | CTGAGGCAGGAGAAT[C/T]GCATGAACCCTAGGT | 8945 |
rs187601239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534599 | GGAAGGGCGCATGAT[A/G]GTCAAATATAGGTAA | 8945 |
rs187612969 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101439880 | TGGGTAAAGAGATGC[A/G]GTGACATAGTTTGTT | 8945 |
rs187625506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417301 | CTCGTTTACTCTGGA[A/G]CAGTTCTTCAGTCTT | 8945 |
rs187627101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483332 | GGGCACGGTGGCTCA[C/T]ACCTGTAATCCCAGT | 8945 |
rs187631186 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101493330 | ATTGAATGTTTATGA[G/T]GTACTAGGCATATAC | 8945 |
rs187637727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379280 | CCTGACACATATGCA[C/T]CTCATCAATAAACTA | 8945 |
rs187652284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445495 | ACTGTAAGGTATAGC[A/G]CAGGGACATAGTGAT | 8945 |
rs187661247 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101370872 | GGTGTGCACCACTTC[A/T]CTGGGCCAAGATGTT | 8945 |
rs187671813 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101530682 | AAGGCTTGGTACTCC[A/G]ATGTTCTACACTGGA | 8945 |
rs187733098 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101529587 | CTGGAATTCTTTCAT[A/G]ACGCATCTTGTTTCC | 8945 |
rs187798624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101403552 | AAAAATTTTATTTTC[A/G]GTTTTCTCATTCCCA | 8945 |
rs187799352 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555490 | CTCTCTCCTGCTGAT[A/G]GAAATGGGAATGAAG | 8945 |
rs187801268 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101365840 | TCATAATCGGAAAAA[A/G]TAAAATTTAGTATAT | 8945 |
rs187826073 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101512680 | TGCAGCTTCAGAGAA[A/G]TTCATGGTAATTTTG | 8945 |
rs187834040 | snp | A/G | 3.31785e-05 | 0.00407286 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535356 | TTTTCTTTTTCAGGT[A/G]TGGAACACAAGTACT | 8945 |
rs187852271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471586 | AGAGTTATGCTGGTC[C/T]TATAAAATGAATTGG | 8945 |
rs187854516 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101446308 | CACATCCTGTGTCCC[C/T]TGCCATTATTGTGAG | 8945 |
rs187868833 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493628 | CCAGGATTTGGAAAT[C/T]GCAGAAGTATGCAAA | 8945 |
rs187874991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409361 | CTTCTTTCACTTACC[A/G]TATTTTTGAGGTTTA | 8945 |
rs187883317 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101426014 | ACATATTTGTCAGAA[A/G]CTGACCAATCAGAAT | 8945 |
rs187898090 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553849 | AAAGTGTACGAAGAG[A/G]GTGTCCTCCTCTCAC | 8945 |
rs187901942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470951 | CTCAAACCTCCTGAA[G/T]AAAACGTTGCTGCTG | 8945 |
rs187910471 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101437831 | GTCTTTGCATATACC[A/G]TTCTGCTTACCTGAA | 8945 |
rs187914675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512376 | TCATTTGCATCTTTC[C/T]TGTCATAAATACTTT | 8945 |
rs187923917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517761 | ATTTTGTCTCCTTTT[C/T]TCTCATACTCATATC | 8945 |
rs187931760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362583 | TATTTTTAGTAGAGA[C/T]GGAGTTTTTCCATGT | 8945 |
rs187933627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399942 | GAATATGTAACTCTT[A/C]ATACTAATGTCCTGA | 8945 |
rs187976813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441110 | TTCTTGTAGAAATTG[A/G]TTTCTCATTGGCTGA | 8945 |
rs187981658 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101541549 | ACAGGCGTGAACCAC[C/G/T]GCGCCCGGCCTAGGG | 8945 |
rs187993156 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101451177 | TGACAGTTGTAATCA[A/G]GTAGCAGTATTAAAA | 8945 |
rs187997066 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101422152 | TTCCTGACTTTTTAA[A/T]GATCACCATTCTAAC | 8945 |
rs187999125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403692 | ACCTCTCAGGCTCAA[C/G]AGATCTTCCCACCTC | 8945 |
rs188003368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101476458 | ACAAGTATATAGGAA[A/G]TCTTTACTTTTTCTT | 8945 |
rs188005446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444182 | TCTTAAATGGTTTTC[A/T]CTTGCCTTTACATAC | 8945 |
rs188011094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496560 | TGCTGGAATTACTGA[C/T]TTTTTTTAAAATTGC | 8945 |
rs188011430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499124 | GAAGTAGGTGGTATT[A/C]GTTTTGTTTACAGGG | 8945 |
rs188011446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101424295 | GCAATAAGGCTGGGC[A/G]GATATGATTATCCTA | 8945 |
rs188031757 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101431202 | CTGCCTCAGCCTCCT[G/T]AGTAGTTGGGATTAC | 8945 |
rs188035701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384782 | TGAGAAGTAAAATAC[A/G]TTGTAGTTAAAAATT | 8945 |
rs188040713 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366909 | ATATTTATATATATT[A/T]ATATATATTTATATA | 8945 |
rs188048855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406126 | TTTTAGGATTATTCT[C/T]GATGAATTAACCTTT | 8945 |
rs188053158 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101455471 | ATAAAGAGATATAAA[G/T]AATTAAGTGCCAATT | 8945 |
rs188086548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384168 | AGCAACTGGTTTTGT[G/T]AAGTCTGTGCAATTA | 8945 |
rs188167258 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101427869 | GCATTTAATAAGTAT[G/T]TATTGAATAAATGAT | 8945 |
rs188175287 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101447623 | TGGTATTTTCCATTC[C/T]ATAACGCAACAAGTG | 8945 |
rs188178915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472894 | TTTATCTTTATCACT[C/T]GTTTTCAGCAGTTCT | 8945 |
rs188183263 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101391325 | TATTACTTTGGAATA[C/T]ATAAAGTTTGGTCAT | 8945 |
rs188190493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370791 | TGTCCAGGCTGGTCT[A/C]AAGCTCCTGGGCTCA | 8945 |
rs188194745 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101411044 | TCTGTCGCCCAGGCT[A/G]AAGTGCACTGGGGCA | 8945 |
rs188200207 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101498296 | GTAGCTGGGACCACA[A/G]ACATGTGCCACCACG | 8945 |
rs188211834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541330 | AGTGGCGCGATCTCA[C/G]CGCACTGCAAGCTCT | 8945 |
rs188227642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101544145 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 8945 |
rs188233574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514404 | GATGTGAAGTTAGGA[A/G]CAGACTTCATTTCCT | 8945 |
rs188241322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421468 | CTCCCTGGGTCTGTT[C/T]ATTTTTATTTTATTA | 8945 |
rs188258080 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464044 | AACACCTGATCTGTT[C/T]ATCTAAACCAATAGG | 8945 |
rs188266088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472003 | CTGAGTATTTCCATC[A/T]TATAGTTTCCCTGGT | 8945 |
rs188358503 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101357748 | AATAAAATCCTGTTA[A/G]TAAGACTGCTGATTC | 8945 |
rs188382010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497198 | ATTGTTTTCTTTGAC[C/G]ATATGCTTATAGGTC | 8945 |
rs188410326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452979 | ATCCTAAAAGGATTA[A/G]TTAAAATTTGTTTAA | 8945 |
rs188435594 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101506210 | GAGCCACCTGTAGTT[A/T]TCGCGCCTGGCTAGT | 8945 |
rs188443306 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101526493 | GCAGAAGTTGGTATC[C/T]TGTGGCTGGGCACAG | 8945 |
rs188446978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101413828 | CGTGTTTTTTTATAT[A/G]CAGGATTTTCATGTT | 8945 |
rs188457685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546965 | ATCAATTTTCTGTTA[C/T]CTCTTCTATAAGATA | 8945 |
rs188515890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101494649 | GCTGGTTTTATACAC[A/G]TATTGATTTTAACAA | 8945 |
rs188554929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522564 | TAGCTGGGACTACAG[A/G]CACCTACCACCATGC | 8945 |
rs188586479 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101508684 | CTTTGGGAGGCCGAG[A/G]CGGGCAGATCACGAG | 8945 |
rs188592989 | snp | A/C/G | 0.00235843 | 0.0342586 | intron-variant | BTRC | GRCh38.p7 | 10:101531354 | AATCTATGTATTTTG[A/C/G]GGTATTGCCCAAGGG | 8945 |
rs188597081 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101500529 | AGATTCATGTATAGA[C/G]AGTTTTCTGAAAGCC | 8945 |
rs188597877 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101368941 | CGAGAATCGCTTGAA[C/T]CTGGGAGGCGGAGGT | 8945 |
rs188604484 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551896 | CCTCACGGAACCCTG[C/T]GAAGGCTGTGTGGAG | 8945 |
rs188668735 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517104 | ACACAAAAAGCAGCC[C/T]TAAACTCCCCCAAGG | 8945 |
rs188668948 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353483 | TTCGGCCCTGACTTG[C/T]TGTGGGGGAGAAAAG | 8945 |
rs188690480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432049 | TGCTTTTATCATGAT[C/T]GTTATAAACATTATT | 8945 |
rs188706504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101475586 | CTTTATAATATCGAT[A/G]GGGAGTTATATATCT | 8945 |
rs188712694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393649 | AAAAACAAAAACAAC[C/T]CACATTTGGTCACAG | 8945 |
rs188748078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365232 | GCATGCACCACCACA[C/G]CCAGCTAATTTTGCA | 8945 |
rs188760899 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436383 | GGCACGGTGATGCAC[A/G]CTTATAATCTCAGCA | 8945 |
rs188791452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381198 | GATTCTAGACACTAT[A/C]TATATTAACTCATTT | 8945 |
rs188813705 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551525 | CCCAGGTGGTCCATA[C/T]ATATTGTGGTATATT | 8945 |
rs188872233 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417089 | TCTGTGTATTTCCTG[C/T]AAACCAGAACATTCT | 8945 |
rs188878392 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352982 | CTTAGCCTCCCACAG[G/T]GCTGGGATTACAAGC | 8945 |
rs188906748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101393341 | CAGCAAATTAATTGA[A/G]CCCACAGAGGGGATC | 8945 |
rs188907636 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101525058 | TAGAAAACCTCTGAT[A/G]TGTACTTTGTAAACA | 8945 |
rs188936560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101461170 | GCCTCCCAAAGTGCT[A/G]GGATTACAAGTGTGA | 8945 |
rs188940442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482496 | CGCCTCCCGGTTTCA[C/T]GCCATTTTCCTGCCT | 8945 |
rs188946294 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505447 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATT | 8945 |
rs188949141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356011 | GTTTTCCTACTTAGA[A/G]GGTTGACTCCTTTTT | 8945 |
rs188956879 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101400927 | CATCTTTCAGAAATA[A/T]CAAAAGCTGAATCTT | 8945 |
rs188964730 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | BTRC | GRCh38.p7 | 10:101438381 | AGTGAGCCGAGATCG[C/T]GCCACTACACTCCAG | 8945 |
rs188967064 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101418786 | CATGGTGTTTTGTTG[C/G]ACCTATCAACCCATC | 8945 |
rs189010666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101510026 | CAAAAATTAGCTGCG[C/T]GTGGTGTTACATGTC | 8945 |
rs189020976 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101552681 | ATAGCAAGAGCACTT[A/C]TAGTGCTCACATCCT | 8945 |
rs189037507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459449 | CCTGATATCATGACT[C/G]TTTAATGTCCCTACC | 8945 |
rs189043561 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389933 | GCCAAACTCTTGCAA[C/G]ACCACTATAAGGCCT | 8945 |
rs189046735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469035 | AGTTTTCAGCAAGGC[A/G]TCTTACTAGTTTATG | 8945 |
rs189052995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101432613 | TCCTACTTCAGAAAC[C/T]AGTTTCATGTTTAGA | 8945 |
rs189078039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442736 | TGTCTTAGCATCATA[A/G]AAAGGATAAATGATA | 8945 |
rs189081056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467045 | GTATTAACAAAACAA[C/T]CACAACAACAAAAAG | 8945 |
rs189086965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487997 | ATTAATAATCTATAG[A/G]CTGTAATTCTATCAG | 8945 |
rs189101984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101404130 | CCGCCTACCGGGTTC[A/G]CGCCATTCTCCTGCC | 8945 |
rs189110129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395488 | TTCTAAAGAAAAGAC[C/T]TTGATCCAGTAATTA | 8945 |
rs189116460 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101359847 | TCAGGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 8945 |
rs189120511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375638 | CTTCAAGCTTGAACT[C/T]AAAAGTGGAACTGGG | 8945 |
rs189122223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423232 | TCTGGGTCTTATTTA[C/T]CTTACTAGTTTATTA | 8945 |
rs189170540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442083 | AAAGCATAGAAAAGC[A/C]TATGTAAGCACTTTG | 8945 |
rs189203031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101412816 | TCAAGGTCTGTTGGC[A/G]ATTAAGTTTATATAC | 8945 |
rs189225110 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101373616 | ATTTAAGATATATTC[A/G]TATAAATAAAGATGG | 8945 |
rs189232876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101473557 | CTTACTGCAACCTCC[A/G]TCTCCCGGGTTCAAG | 8945 |
rs189234573 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101495770 | ATAGTGAATTTTCAC[A/G]AAGTGAACATACCTG | 8945 |
rs189244734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515345 | AGTTAATTTGCCTGC[C/T]GAGACTTTGATATTG | 8945 |
rs189245454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507978 | AAACTGCTGTGAATT[C/T]CTTGGTTTAGAACAA | 8945 |
rs189253988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429011 | TAAACAGTGAATACC[A/G]TATTTTGTTTCCCAA | 8945 |
rs189273514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448082 | TCAAATTAATTGTAG[C/G]ATTTGTCAGAAATGC | 8945 |
rs189289775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490704 | TCTTCCTACCTCTTG[C/T]TGCTTGTATAAATAT | 8945 |
rs189302198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531808 | AATTTTAAAGCTTTA[A/G]AAAATGGTTTACTAA | 8945 |
rs189339666 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415264 | TACTTCAGCCTCCAC[A/G]TTCCAGGCTGAAATG | 8945 |
rs189351491 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101495291 | TTCTGAATTATCTAA[C/T]ATTATAGCAGTTATA | 8945 |
rs189356396 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | BTRC | GRCh38.p7 | 10:101462443 | CCACCACTTTGGGAG[G/T]CTGAGGCAGGCGAAT | 8945 |
rs189369612 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101537288 | ATCCCAGCACTTTGG[A/G]AGACCGAGACAGGTG | 8945 |
rs189399333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539241 | ATTATTTATCATGTT[C/G]TTAGCCAAGGGCCCA | 8945 |
rs189426683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101400609 | TCAAAGGATTTTACT[C/T]TGGCTTATTTGGCTG | 8945 |
rs189462773 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101363273 | ATCCTGAGATTAAAT[C/T]CAGGCAGTCTGACTT | 8945 |
rs189464391 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101380006 | TTGCTGAATGGACTA[C/G]TTATAACTTCTTTTG | 8945 |
rs189506188 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443505 | TGTGCATACAAAACC[A/G]CTTCAGTAAAAGTGC | 8945 |
rs189514653 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101489839 | ATCCTGTTTTTGAAG[A/G]CATCTTTTTTTGTTT | 8945 |
rs189544137 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404850 | AAAAATACAAAAAAT[G/T]AGCCGGGCGTGGTGG | 8945 |
rs189563394 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366889 | ATATTTATATATATT[A/T]ATATATATTTATATA | 8945 |
rs189640732 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439217 | AGCTTTTTGTTTTCT[A/G]AGATGGAAACACAAA | 8945 |
rs189646539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515037 | CTCGGCTCACTGCAG[C/T]CTCCACCTCCCGGGT | 8945 |
rs189650640 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557399 | GGAGTGCAGAGATAG[A/C]ATACCTTTGCAGATA | 8945 |
rs189651393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101501231 | ACGCCAATATGATGG[A/G]TTTTAAGTAAGAACA | 8945 |
rs189656017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483125 | GACCCCTATAATACC[G/T]TGATTGTAACTCTTT | 8945 |
rs189659535 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471515 | TTTTGTGTCTGTTTC[A/G]TGTGAGGTACTGGTT | 8945 |
rs189660991 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101519722 | GGGGACCAGCCAGGT[A/G]CAGTGGCTCACGCCT | 8945 |
rs189663756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520620 | AGAGTCTCAGAATAT[C/T]CATTGGTTTCTTTTC | 8945 |
rs189670179 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101542836 | GTACTGGGATCACAG[G/T]CATGAGCCATGGCAC | 8945 |
rs189690439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101478792 | ATCTCAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA | 8945 |
rs189707993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101427055 | ATTTTTTTCTACCCA[A/G]CACACACAGAAACTT | 8945 |
rs189789569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468051 | AAGAAAACACGGTTT[C/G]GCAATTTGTGCCTAG | 8945 |
rs189805742 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387222 | TAAAAATTTAACATA[A/T]TAAGTGTACATATTT | 8945 |
rs189810133 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101423561 | CCTTGAAATAGAGTG[C/T]AAACTACTTGAGTCT | 8945 |
rs189813313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101528768 | TACCAAGCCTAATAC[A/G]TCAATAAAGTCTTTC | 8945 |
rs189827185 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441706 | GTAGCATGGTGAAAC[C/G]CAGTCACTACTAAAA | 8945 |
rs189833064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546283 | AGCATATGCTCTCAG[A/G]TTACAGTGGTATTCA | 8945 |
rs189851006 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101549833 | CTACATCTTCATCAG[A/G]GTGGTAACTGCCAGT | 8945 |
rs189866947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372905 | TCCACAAAACATACT[C/T]TTATGATTTTTATTG | 8945 |
rs189868695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355441 | TTGGCAAACTCGTAT[A/G]GTCTGATATTTGATG | 8945 |
rs189935061 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101541984 | ATTTTCTAAGAGTTT[G/T]CATATGTGATATTAT | 8945 |
rs189963467 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101409899 | ATGTATTTGTTTACC[C/T]GTTTTTAATTCTTTG | 8945 |
rs189983750 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369627 | ATCTGGGTGTTAAGC[A/C/G]TGCTCATTGCTATTG | 8945 |
rs189989115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101415597 | CCCATGCTGGAGTGC[A/G]ATGGCGTGATCTCGG | 8945 |
rs190004748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101449731 | TCTGAAATCCCCCTG[A/G]TGAATTTTAATTCAT | 8945 |
rs190005016 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475203 | TTTTACTTAAATTAT[A/G]AGAATAAAACAAGTT | 8945 |
rs190007124 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | BTRC | GRCh38.p7 | 10:101456063 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8945 |
rs190018963 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496430 | GTTTTAAGTTTTTAT[G/T]TTAGAGGCATGGCTT | 8945 |
rs190026729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412491 | TCAGTTTCTTGATGG[C/T]AGGAAGATAAGTTTG | 8945 |
rs190030748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393079 | CACTGAGAGGGTCCC[A/T]CCTCATACCCTCGTG | 8945 |
rs190046026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101430646 | ATCCACTCTTAAGAC[A/G]ATGTCATCATGATTG | 8945 |
rs190051315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385832 | CTGATCTAGCTTGTT[G/T]TTTTTTTGATTCTTG | 8945 |
rs190147449 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101456869 | AGTTGTGCACTGGGC[C/T]AAGAAATAAATATTT | 8945 |
rs190148172 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101541623 | CTGTTCCTAGATTGC[C/G/T]GAGAGTTTTAATGAG | 8945 |
rs190159109 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101534037 | ACCTTAAGTAAATAC[A/G]CAAAAATAGAATAAT | 8945 |
rs190163948 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101477940 | CAGGTATGAGCCACC[A/G]CACCTGGCCTGATTT | 8945 |
rs190173823 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367334 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 8945 |
rs190174004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101415902 | ATACACAAATACTTT[C/T]CACTATATTGCAGTT | 8945 |
rs190176818 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500137 | GTATGAAAATGTGTC[A/G]TTAGGCAATTTTGTT | 8945 |
rs190178517 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101396362 | AACTTTATGAATTTC[G/T]GCAAGATTCTGCCAC | 8945 |
rs190186577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101434503 | AAAATGTGGCAAAAA[C/T]AATCATTGTGACTTT | 8945 |
rs190190120 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553451 | CATTGGTTCCAGACA[A/G]AGGTGACTTATAAAT | 8945 |
rs190213265 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377289 | TGTACCAGACTGTTT[A/G/T]TTCACTCCTGAAGGA | 8945 |
rs190263321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101434343 | AAATCCATTGGTCTC[A/G]GTTTTTTTCAATAAA | 8945 |
rs190291271 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523734 | TTGTGACCATTTTTT[C/G]TTAATACATTCTCTT | 8945 |
rs190306250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485214 | AAAAAGTCCAGACCC[C/T]AGCCCAGAATCTTTA | 8945 |
rs190317513 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101506757 | GATGAAGTGCTCTAA[A/G]CAACTGAAGTTTACT | 8945 |
rs190325680 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101527021 | AAATACTTTTCTCTC[A/C]GAGTATGTCTCTAGA | 8945 |
rs190338069 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101420320 | GCTGACATATCTCTC[A/G]CTCCATTTCTCACCC | 8945 |
rs190341442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371353 | CAGCTAATTTTTGTA[G/T]TTTTAGTAGAGACGA | 8945 |
rs190346288 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101440615 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGTGGG | 8945 |
rs190349983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463778 | TTCCAAAGCGTTTCT[A/T]CTTGTGCCTTCTGAC | 8945 |
rs190359447 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101438197 | TTTGGGAGGCCAAGG[A/G]GGGCAGATCACAAAG | 8945 |
rs190368596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402576 | AATAATTCCTATCTT[A/T]AAAATTCTATATTAG | 8945 |
rs190391440 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101518467 | AAGTCCCAGAATGGA[A/G]TGCAACTTTCTCCCC | 8945 |
rs190421784 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101477207 | GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTCAA | 8945 |
rs190468319 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549292 | AAAAAAAAGCCAGGT[A/G]TGGTGGCATGAGTCT | 8945 |
rs190500186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358969 | CTATGCTAGTTGGAT[A/G]TTAAGGCTAAAAATA | 8945 |
rs190506508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394577 | ATACATAGTCACAGA[A/C]TGACTAGTAATGAGT | 8945 |
rs190508269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361685 | AATTAGAATAGTCTG[A/G]GGCTTATTCCTTTTA | 8945 |
rs190515603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101371572 | TAGCTTATTTTACTT[A/G]ATGTCCTCAGGTTTC | 8945 |
rs190529748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101355309 | ATTTGTGGTTACCCG[G/T]CAGTTTTAGGTTGAA | 8945 |
rs190549322 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101545811 | CTAGTCAGAAGAAAG[G/T]TGGGGTAGCTGTATT | 8945 |
rs190565376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460491 | AATATAGCATGCTTT[C/T]TCTTTAATTTTAGGG | 8945 |
rs190582246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504536 | TTATCCCATCTCTCA[C/T]CAACCCCACTGCCTA | 8945 |
rs190590615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101418655 | ATATATGTTTATATT[C/T]TTTCTCCCTGGCTGT | 8945 |
rs190605952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391890 | CACATATGGTTAGTT[C/T]AATATTATTTTTACC | 8945 |
rs190612023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101553113 | AGCAAGTAAGAAATA[C/T]CAAAAAAGGGGCTAA | 8945 |
rs190617358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101435776 | AGAGACAGTGAAGCA[A/G]TTCTTCAAAGTGGTT | 8945 |
rs190624508 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101354865 | GGAAGAGGCCTCACT[A/G]AAGAAGATAAGGACT | 8945 |
rs190639536 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101398309 | TCTTTTTTTCTTTTT[C/T]TCTTTTTTTGTTTTT | 8945 |
rs190657341 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101491651 | GCAGTGAGCCAAGAT[A/C]GCGCCTCTGCACTCC | 8945 |
rs190661746 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101360987 | TATTTTTATTTTTTT[A/G/T]TAGAGATGGGGTCTT | 8945 |
rs190665435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101510532 | AACAAAAAAAAAAGT[C/T]GTTGTTAGATGTTTA | 8945 |
rs190671382 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101532543 | GAAAGTAAGTGAAGA[G/T]TTTAGATTGTTTCCA | 8945 |
rs190682453 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101424527 | CTTTTTATTGTTGAT[C/T]ATTATAGCTTCTGTT | 8945 |
rs190684542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417215 | GTAATCTCAGTCAAT[A/G]TCCTTTATATAATAG | 8945 |
rs190690747 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469577 | TTATTGATGACTGGA[C/G]AAACCTCTGTAAAAA | 8945 |
rs190692816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444473 | TTGATATAAAAATTC[A/G]TAGAAACCTGTTTTT | 8945 |
rs190694503 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101399136 | TTTTTTGTATTTTTA[G/T]TAGAGATGGGGTTTC | 8945 |
rs190738447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101375302 | CTCTTCTTCCTGCTT[C/T]GGCCATATAAGATGC | 8945 |
rs190739486 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554276 | TGGCCAGAGCCAATC[A/G]CTTGGTGCATTCTGC | 8945 |
rs190760129 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101512458 | TGTCTTTCTCTACTT[A/T]CTATACCCTTCCTTT | 8945 |
rs190790852 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101382337 | GGATCCAATCATGTT[A/C]TATATAATATCTCTT | 8945 |
rs190795205 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440239 | CTTTTTTTTCAAGCT[A/G]TGAGTAGGAGTTTAT | 8945 |
rs190796618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101419460 | AAAAAGCCACTTCCA[A/G]GCTTATTGTTGTTGG | 8945 |
rs190823354 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101383201 | CCTTAGTAGCTGGGA[C/G]TACAGGCGTGCACCA | 8945 |
rs190833738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101419922 | CCTGTCCAAGCCCTC[A/G]CATTGTTCTAAGGAG | 8945 |
rs190841925 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101401745 | TCTGAGGCTGAGTCG[C/G]GAGGATCTCTTGAGG | 8945 |
rs190848947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493367 | ACTGAAATCATCACA[A/G]TAGTCTCATTGTGTT | 8945 |
rs190853825 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101365212 | CTGAGTAGCTGGGAT[C/T]ACAGGCATGCACCAC | 8945 |
rs190870563 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101458602 | CCTCAACAGTGTGTG[C/T]TATACCTCTTTAGTT | 8945 |
rs190909276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416824 | TTAGTTGTTCTCTCT[C/G]TCATGGCTTCCATTT | 8945 |
rs190916338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101540581 | CTTTTTCAAAGTTTT[C/T]TGGGGCCTTTGATTT | 8945 |
rs190924827 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101377975 | TATATGCCTGTAATT[C/T]TTTTAAAGCAGAAAT | 8945 |
rs191014575 | snp | C/T | 0.00246189 | 0.0349983 | intron-variant | BTRC | GRCh38.p7 | 10:101534625 | GGTAACAGATTGTAG[C/T]TTGAGTACCATCTAA | 8945 |
rs191031339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401311 | AATTCTTTACTTAGC[A/G]TAAGGTGATTTTTAA | 8945 |
rs191059270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101363919 | CAGTTAGCTATTGGC[A/G]TTTAGAATCACAAAA | 8945 |
rs191090154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101516906 | TCATGTCCATTTCCA[C/T]CTTTTAAAAGACAAA | 8945 |
rs191091639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408013 | AGGCGTGAGCCACTG[C/T]GCCTGGCCTAAACAT | 8945 |
rs191093606 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101445086 | GACATTTCATTTGAA[G/T]ATACGACTATATATT | 8945 |
rs191100208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101540714 | GTTGCCCAGACTGGT[C/T]TCAAACTCCTGGCCT | 8945 |
rs191123843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475450 | TAGGCTGAGGCAGGA[A/G]AATCACTCGAACCTG | 8945 |
rs191127976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496614 | AAAATTTACCATCTT[A/C]CTATTTTTAAGTATA | 8945 |
rs191156075 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101516411 | CCAGGTCTTTTTACT[C/T]CAGGGCCAAAGCTTT | 8945 |
rs191241225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545323 | TTGAAGAAGAAGGCT[A/C]AACTTATGTTGTCTA | 8945 |
rs191256509 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | BTRC | GRCh38.p7 | 10:101408990 | GGAGACGGAGGTTGC[A/C]GTGAACCAAGATTGT | 8945 |
rs191268525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492899 | GACACTAGAGGAGCT[A/G]CTGTCTCAACATTAT | 8945 |
rs191270907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445532 | CAGTTCACTTCACCC[G/T]CCTGAAACTAAGAAT | 8945 |
rs191275263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425914 | AGTCCAAACTTTAAG[C/T]AGAAAACTATGTGCT | 8945 |
rs191281187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101523232 | ATAAATAAATAGATA[A/G]ATAAATTCTACAGAT | 8945 |
rs191288952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389277 | GATTTTATCTGTTCT[A/G]CTTCCAAAATACATC | 8945 |
rs191294948 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352586 | TTATATGCTTACCAT[C/T]TGTTGGATGACTGAG | 8945 |
rs191300403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368006 | AATGTTTAGCTTTAT[G/T]CTATGGTTTGAATAT | 8945 |
rs191328113 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424950 | TTTCAAGCTTTACCC[A/C/G]CTTTGTCCTCCCACC | 8945 |
rs191368577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389029 | TAATGGGCTAATAGT[C/T]TCTAACCCATCCTTT | 8945 |
rs191385083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476026 | CCTTAGCTGTATAAT[C/G]AAGGCTAACATCACC | 8945 |
rs191392982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498450 | GTGAGCCACCACACC[C/T]GGCCTCCGAAGCTGC | 8945 |
rs191397012 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101517786 | CATATCCAGTCGATC[A/G/T]GCAAATTCAGTAGGA | 8945 |
rs191406353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432300 | TTGGCTCATTTTTCT[A/G]TTTTTTTTGTGGAGA | 8945 |
rs191407903 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101474298 | TTTTGTATTTGTTAA[G/T]GTCAGGTGTATTTTG | 8945 |
rs191420677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101453965 | GTAAATGGATGGGCA[C/T]GGCTATGGGCCAGTT | 8945 |
rs191430449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515646 | CCTCCAGAGTAGCTA[C/G]GGCTACAGGCATGTA | 8945 |
rs191435899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375064 | ACCAGGTGTGTGGAC[A/G]CAGGGGAACTTAGCA | 8945 |
rs191446331 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415008 | TAGTCTAGCCTAAGT[C/G]CACAGAGTTTATTGG | 8945 |
rs191447636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365512 | CGAAGTTTCGCTCTT[A/G]TTGCACAGGCTGGAG | 8945 |
rs191451691 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101429340 | ATAATACTAATGTCA[A/G]TTACTTAGAGCTACT | 8945 |
rs191454252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394061 | ATAGATTTTATAGAA[C/T]GCAGACATTGTTTAG | 8945 |
rs191474891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392213 | TCAAACTCTTGACCT[C/T]GTGATCTGCCCGCCT | 8945 |
rs191496486 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101470745 | CTTTATAAGTTTACT[A/C]TTTATACTTAATTCT | 8945 |
rs191516902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511847 | ATAGAGACGAAGTTT[C/G]ACTATGTTGACCAGG | 8945 |
rs191580528 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353583 | GCTGCCAGGTGCCCA[C/T]TGGCCCAGCTACTCT | 8945 |
rs191590782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101369888 | AATCAGCCCCTTTCT[A/G]TGTGACCACTCTCAT | 8945 |
rs191598269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399544 | ACCTATATTCCGTGT[G/T]CCTAGCTGTTGTTGC | 8945 |
rs191601758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388142 | ACTAAAATTTGAGAA[C/T]TTTTAGCTAGGAAAG | 8945 |
rs191635087 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101539831 | ACTCCACATTCTTGC[C/T]AGTACTGAGCACAGT | 8945 |
rs191673383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496176 | TTCTTTCAGATTTTC[A/G]TAACTACAAAAAATT | 8945 |
rs191681436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383973 | TTCCGTCTCAGCCTC[C/T]CAAATAGTTGCCGGT | 8945 |
rs191693679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412358 | CCTGGACAGTACCTT[C/T]GGGTAGAAGACTAGG | 8945 |
rs191698456 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101448952 | TAATTTTAAAGACCC[A/G]AAGAGACATTAAGGC | 8945 |
rs191723417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101502042 | AATGGTGCCCATGTA[A/G]GGGACATATAAATAA | 8945 |
rs191734716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101543216 | TTATTGGGTACCTGC[A/G]TGCTTAGGATTTTTG | 8945 |
rs191740404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479962 | GCTACCTCTTTTTCA[G/T]GTATATATGTCATCT | 8945 |
rs191744710 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503241 | AGTCTCAGTGCATAT[A/G]TAAACCTCTTTTGGT | 8945 |
rs191753478 | snp | A/G | 0.00441676 | 0.0467854 | intron-variant | BTRC | GRCh38.p7 | 10:101459468 | AATGTCCCTACCTCT[A/G]TTTTTTTGTAACAAC | 8945 |
rs191754655 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101522650 | GGTCTCAAACTCTTG[A/G]CCTCAAATGATTCAC | 8945 |
rs191762929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437290 | ATTATGGAATATGTA[A/C]ATTATTTGGTAAATA | 8945 |
rs191765171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391155 | TCCTGTGTGGTAACT[A/G]CCGCTCCTGCTGTGA | 8945 |
rs191767262 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101417253 | ATCTAGTTCAGGATC[A/G]CATGATACATTTAGT | 8945 |
rs191785012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460011 | CCAAGTTATATGATA[A/G]CATTTCAAAAAACAT | 8945 |
rs191823724 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556815 | GTCCTGGAGGCAGAT[C/G]ACATCTAAAATATGT | 8945 |
rs191880685 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367071 | ATAAATATAAATATA[A/T]ATATATATATTTTTT | 8945 |
rs191887179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407050 | CTTTTAAATTTTCTT[A/G]TAGCCACATTGAAAA | 8945 |
rs191900194 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101413420 | CAGGGTTTACACCAT[C/T]CTCCTGGCTCAGCCT | 8945 |
rs191905155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101393660 | CAACCCACATTTGGT[C/T]ACAGAGAAGTCTTCT | 8945 |
rs191915367 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101374003 | AGGTGGAAAGCTGGG[A/T]GATGATTAGATGGAG | 8945 |
rs191937393 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101357002 | GGTGTGGCAGCGTGC[C/G]CCTGTAGTCCCAGCT | 8945 |
rs192020802 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101522081 | CCTGTCGCCCAGGCT[A/G]GAATGCAGTGGTGTG | 8945 |
rs192027786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483860 | CCTTCATGATTTTTT[C/T]TAATTGGTAAAGAAA | 8945 |
rs192034325 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101452287 | TTATTTCTCTTTGCT[A/G]CTGATCCAAATGGTT | 8945 |
rs192038919 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101526702 | GGAGAATCGCATGAA[A/C]CCTAGGTTTCTTTCA | 8945 |
rs192048098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436920 | CATTATTCATTATAT[A/G]TATGGAAAACTTAAT | 8945 |
rs192056444 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101479562 | ATTACAGGATTATAT[A/G]GTTAAGAAAAAAATA | 8945 |
rs192114470 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101508611 | GATCACTGAGAGTTA[C/T]AAAGTTTAAGAACTA | 8945 |
rs192118829 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101531064 | TAATCACAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8945 |
rs192136983 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551622 | CTAGCTGCTGAGGAG[C/T]GTTGCTGTCAGGATT | 8945 |
rs192139463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101443134 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 8945 |
rs192141211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467692 | AAGTGCTTTGGGCTT[C/T]GGGTAAAAAAAAAAT | 8945 |
rs192153141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101488010 | AGACTGTAATTCTAT[C/T]AGGAGTCATTTGATT | 8945 |
rs192155725 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101437868 | CCTCCACAAACACCT[A/G]TTGTCCCTTACCCAC | 8945 |
rs192170616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400171 | TTCATATATTGTAGC[G/T]GCCAATCAGTCAGTG | 8945 |
rs192175855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362756 | TAACAGCTAACAGCT[A/G]GTCCCTCATATTTGT | 8945 |
rs192199553 | snp | G/T | 0.105924 | 0.204309 | intron-variant | BTRC | GRCh38.p7 | 10:101463050 | TTTTTGTATTTTGGG[G/T]TTTTTTTTTTTTTGA | 8945 |
rs192201502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101431452 | AAATAATGTGGAAAA[C/T]TGTAGACAAAAACGT | 8945 |
rs192264978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512956 | TGAACAGTAGTGGTT[C/G]AGTCATCAGGCTTTT | 8945 |
rs192274765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535797 | TTTTGTCTTAGCATT[A/C]CATAATTGGCCAGAG | 8945 |
rs192286360 | snp | G/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556423 | TTGGACTAGATACCT[G/T]GGTACTGTTGACCTT | 8945 |
rs192293576 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101446856 | TCTATCCCCCAAAGA[G/T]CTAAACCAGGAATTT | 8945 |
rs192295060 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101438222 | ACAAAGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 8945 |
rs192300765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493731 | CCTTTCTAGCATTCC[A/G]TATGAGATGATAAAA | 8945 |
rs192300973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101481223 | AGTTGGGATTACAAG[C/T]GTGAGCCACTGCACC | 8945 |
rs192379506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101506490 | TTTTCAGCCCTGTTA[C/T]CAGTCTTGGGGGTGG | 8945 |
rs192399463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548684 | TTGAACCTGGGAGGC[A/G]GAAGTTGCAGTGAGC | 8945 |
rs192449806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464123 | TACAGAAACAACTGT[C/T]GGAAAACAATGACAC | 8945 |
rs192455174 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385730 | TCCTTCCTCTTCCCA[C/G]ACACACACACACACA | 8945 |
rs192461346 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366814 | TATATATATATTTAT[A/G]TATATTAATATATAT | 8945 |
rs192461733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507125 | GTTTTTTCTTCTCTT[A/T]CTTCCCCAAGTCTGT | 8945 |
rs192472426 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | BTRC | GRCh38.p7 | 10:101421759 | AGTTTGCTGAGAATG[A/G]TGGTTTCCAGCTTCA | 8945 |
rs192499804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101541551 | AGGCGTGAACCACCG[C/T]GCCCGGCCTAGGGTT | 8945 |
rs192509500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358123 | TTATTTTTGTTTTCA[C/T]CTTTGAGACAGGGTC | 8945 |
rs192516553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417827 | ACAGATGCGTGTCAC[A/C]ATGGCTTCTTTTTTT | 8945 |
rs192519681 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101384385 | AAAGTTTAATTTCAC[A/G]CCCTGATTAGTGCCA | 8945 |
rs192537152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460389 | TTCCTCCATTTTTTG[G/T]TAGATGATCTCCATT | 8945 |
rs192548015 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101518223 | GGCCGAAGTAGTGTC[C/T]TAATTGGCCTCCTTC | 8945 |
rs192558431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465623 | ATTTTATGCCAGACC[C/T]TTTCACAGAATAGAG | 8945 |
rs192574073 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379357 | TAAGTACTCTTAAAT[A/G]TGTTCTACTAATGTC | 8945 |
rs192583175 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404004 | TATGTGTGTGTGTGT[A/G]TATATATATATATAT | 8945 |
rs192589754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442137 | TATCAGAGTGGCACA[G/T]GTATTTTAAACCTAG | 8945 |
rs192593225 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101422943 | CTTAGGATTGACTTG[A/G]CAATGCGGGCTCTTT | 8945 |
rs192596685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541335 | CGCGATCTCAGCGCA[C/T]TGCAAGCTCTGCCTC | 8945 |
rs192629715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379106 | ATTGAGAAGAATCCT[C/G]CTTTATCAAATTTTG | 8945 |
rs192727290 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101494834 | GCAGAGGATTACAGC[A/G]TCACATCTAAATTAT | 8945 |
rs192730897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101536796 | CATATTTCTTTAATC[C/T]GTGTATTTACCTCTC | 8945 |
rs192732825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101447048 | GCAGCTAGTGTTCGC[A/G]TGCAGGTTGGACTTT | 8945 |
rs192754346 | snp | A/C | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101410164 | GATAAAGCTTCTTCT[A/C]GTACATCTGGATTTC | 8945 |
rs192781515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486968 | ATATTGTGAATATCT[A/G]TGATACTAGGATTAG | 8945 |
rs192801989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101441640 | ATCCCAGCACTGTGG[A/G]AGGCTGAGGCGGGCG | 8945 |
rs192803865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404320 | CAGGTGTGAGCCACC[A/G]CGCCCAGCCAATCCT | 8945 |
rs192807906 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101432197 | CAGTGGCACAATCTC[A/G]ACTCACAGCAACCTC | 8945 |
rs192810165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403589 | TCTTCCCCTGACCCC[C/T]TTTTTTTACTTCCCC | 8945 |
rs192812328 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101365873 | AGTATATGCATTTAT[A/G]AAACAAAATGATCAT | 8945 |
rs192814975 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | BTRC | GRCh38.p7 | 10:101475849 | GGCATGATTAGCACC[C/T]AATGGATGCTAAAAT | 8945 |
rs192870130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101362314 | TTTGGCTTTCCTTTC[A/G]GGGTATCTGATTTTG | 8945 |
rs192897708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517203 | AGAAAACATCCACCT[C/G]AACACACCAGGATTA | 8945 |
rs192927200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544342 | GCTTAAAGAACTTAC[C/T]TTAACATTTCATGTA | 8945 |
rs192931374 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514597 | AGCTAGGATTATAGG[C/T]GTGTGCCATGATGTC | 8945 |
rs192941675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101427203 | GCTCACTGCAACCTC[C/T]GCCTTCCGGGTTCAA | 8945 |
rs192944533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101472058 | CATGAATGTATGATT[C/T]CCTTTAGTGCAGAAT | 8945 |
rs192954288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460900 | ATATATTAACTGTAA[A/G]TTTTTTGTTGTTGTT | 8945 |
rs192962514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504883 | AGAATTCTCTAGATG[A/G]CACAGATACACTCCC | 8945 |
rs192981074 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101390235 | GAAGCTGATGATAAA[C/T]TGCCCATCCTGCTTC | 8945 |
rs192983885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426047 | CCCTGAAATGTATAG[A/C]CTTAATAAGGATAGT | 8945 |
rs193000570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353118 | GCTACAATTTGTTCA[C/T]ACAACCACCTGCTGA | 8945 |
rs193015135 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | BTRC | GRCh38.p7 | 10:101453017 | CACAGTGTTTTTTTT[A/T]AATGTCACCTTTCAT | 8945 |
rs193017400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101386758 | GTCTTTGTTTTGTTT[A/G]TGGTTTAGCTTGTGT | 8945 |
rs193023248 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101423348 | GCTTGTTAGTTTGTT[A/T]TACAGAGAATGTTAT | 8945 |
rs193030855 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101413915 | TGAATATCTTAAATA[C/T]GGTTATTTTAAAGTC | 8945 |
rs193046049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545881 | CAGGGATAAAGAGAA[A/G]TGTTGTATAAGGATA | 8945 |
rs193071982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373644 | TGGGCAGGGCCGGGC[A/G]CGGTGGTTCACGCCT | 8945 |
rs193105932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529776 | TAACAGGGAGAGGGC[A/G]GGGGAGAAACACTCC | 8945 |
rs193116070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487694 | GTGAAAAGATCAGGT[C/G]GGGTAAGCAGGGATC | 8945 |
rs193118512 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497577 | CAGGCATGGTGGTGC[A/G]CACCTGTAGTCCCAG | 8945 |
rs193153692 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101541112 | TTTTTTTTTTTCTTA[A/G]TTGCACTGGCTAAGA | 8945 |
rs193181503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482235 | CATGTTGGCCAGGCT[A/G]GTCTCGAGCTTCTGA | 8945 |
rs193192857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101409477 | GGGGATACATTCTGA[A/G]AAATGTGCCATTAGG | 8945 |
rs193202574 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101369001 | TCCAGCTTTGGCGAC[A/C]GAGCGAGACTCCATC | 8945 |
rs193224182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101523830 | ATGGTTGAAGCACAT[A/G]TTATTTAACCCCTTT | 8945 |
rs193230885 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101393387 | TGAAGCCAGTCAGTC[A/G]GAAGCTCCAGAGGCC | 8945 |
rs193235392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356020 | CTTAGAGGGTTGACT[C/T]CTTTTTTTCTTCTTT | 8945 |
rs193255798 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101550484 | AGATGGGGTTTCACT[A/G]TGTTAGCCAGGATGG | 8945 |
rs193271502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507640 | TCTTGTAATTAGTGC[G/T]GTCATGGAAGATTTT | 8945 |
rs199507010 | in-del | -/ATCATCTGTCCTG | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406935 | TCGGTTTTTAAATTA[-/ATCATCTGTCCTG]ATCATCTGTCCTGAT | 8945 |
rs199507553 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | BTRC | GRCh38.p7 | 10:101472275 | TTTTCTTTTCTTTTC[C/T]TCTCTTCTCTTCTCT | 8945 |
rs199511453 | in-del | -/A | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352132 | TTTATTTATTTATTT[-/A]TTTTTGTAACTCCAT | 8945 |
rs199560320 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101547333 | ATGGTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT | 8945 |
rs199579402 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411687 | TTATAGCTGTTTTAA[C/T]TTTTAGGTCTGCTAA | 8945 |
rs199587113 | in-del | -/AT | 0.206029 | 0.246103 | intron-variant | BTRC | GRCh38.p7 | 10:101505640 | AATAAAAAAAAAAAA[-/AT]AATAATAAAAAAACA | 8945 |
rs199609545 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101413338 | TTTGTTTTTTTGACA[A/G]AGTCTCGCTCTGTTG | 8945 |
rs199622466 | in-del | -/T | 0.0614824 | 0.164198 | intron-variant | BTRC | GRCh38.p7 | 10:101388656 | ACCACGCTTGGCTAA[-/T]TTTTTTTGCATTTTT | 8945 |
rs199626265 | in-del | -/TAAAAC | 0.0126979 | 0.078662 | intron-variant | BTRC | GRCh38.p7 | 10:101483300 | GCCTAAGAAAAAATT[-/TAAAAC]TAAAAATGGCCGGGC | 8945 |
rs199647756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101535700 | GTTGAAAAGTGCTAA[C/T]AAACAGCTAACAGCC | 8945 |
rs199675862 | in-del | -/GT | | | intron-variant | BTRC | GRCh38.p7 | 10:101481559 | TCTATATGATGTGGA[-/GT]GTTTTTTTTTTTTAA | 8945 |
rs199711773 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101484172 | ACTGTTTTTTTATTT[A/C]AGACTAATAATCTGT | 8945 |
rs199725518 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463047 | TAATTTTTGTATTTT[-/G]GGGTTTTTTTTTTTT | 8945 |
rs199748349 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101544408 | GTTTACTTGGGAAAG[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs199806547 | snp | C/T | 0.00044469 | 0.0149046 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534727 | TGAAGCAGTTCTGCA[C/T]TTGCGTTTCAATAAT | 8945 |
rs199816746 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101372461 | GGTTTCACCATGTTG[C/G]TCAGGCTGGTCTCGA | 8945 |
rs199824135 | snp | A/C/T | 0.00199153 | 0.0314936 | intron-variant | BTRC | GRCh38.p7 | 10:101536692 | AAAAGAGAAAATCTA[A/C/T]GTCTTAATCCTTCCT | 8945 |
rs199850714 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428585 | ACTGAGGGATGGATG[G/T]AGGCAGGAGGAAGAA | 8945 |
rs199852989 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420581 | TTACAGTTCCTACGT[G/T]GTAGCCTTCCTTGTT | 8945 |
rs199858211 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101379577 | TATACTACATATTTT[G/T]TTTTCCTAAGAAGCT | 8945 |
rs199879498 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101399016 | GGAATGCAGTGGTGC[A/C]ATCTTGGCTCACTGC | 8945 |
rs199907049 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101354786 | AGAATGAGGAGGGAG[A/G]ATAGCCTTTGCCTTG | 8945 |
rs199968647 | in-del | -/TT | 0.0154538 | 0.0865337 | intron-variant | BTRC | GRCh38.p7 | 10:101395513 | TAATTAATTTTGCTC[-/TT]AACATTTACAGACCC | 8945 |
rs199978694 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101483679 | TGAGATACCTTTTTG[-/T]TTTTTTTTCAGAATT | 8945 |
rs199980484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406003 | TTGCTTATTCTATCA[A/G]TAGCTGAGAGAGTTA | 8945 |
rs199984817 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363466 | TTTGTTTTTGTTTTT[-/G]TCTTTTTTTTGAGAT | 8945 |
rs199987059 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101374070 | AGTATCCATGATAAG[A/G]GGTTAAGAAAAGTTT | 8945 |
rs199989008 | snp | A/G | 0.000214651 | 0.0103576 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532350 | AGAGAATTCACTGCC[A/G]AAGTGAAACAAGCAA | 8945 |
rs200006280 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541278 | CTCTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 8945 |
rs200012831 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362499 | CTCCCGGGTTCAAGC[G/T]ATTCTCCTGCCTCAG | 8945 |
rs200016759 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352965 | TCAGGTGATCCACCC[A/G]CCTTAGCCTCCCACA | 8945 |
rs200018267 | in-del | -/CATA | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101408209 | AGAGTATGTTTAGAC[-/CATA]CATTTAGTGTAGTGA | 8945 |
rs200076147 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528083 | CTGTATCCCTCAGAA[A/G]AAAAGAATCTCGTCT | 8945 |
rs200098478 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101414210 | CATATAAGTGGATTT[-/A]TACAGTACAGGCATG | 8945 |
rs200136139 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415546 | GTTATGTTATGTTAT[G/T]TTATGTTATTTTGAG | 8945 |
rs200146282 | snp | A/G | 0.000625772 | 0.0176775 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534878 | TTTGATGACAAGTAC[A/G]TTGTTTCTGCATCTG | 8945 |
rs200155776 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366788 | TATATATATATATAT[A/T]TTTTTACATTTATAT | 8945 |
rs200186751 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372418 | CACCACCACGCCCGG[C/T]TAATTTTTGTATTTT | 8945 |
rs200187591 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101521104 | AGACTCCATCTCTAC[-/A]AAAAAAAAATGTTAA | 8945 |
rs200193799 | snp | A/G | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535398 | AAGGACCTTAAATGG[A/G]CACAAACGAGGCATT | 8945 |
rs200193907 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101388335 | ACCCAGCTAATTTTT[A/T]TTTTATTTTATTTTA | 8945 |
rs200211236 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101481573 | GAGTTTTTTTTTTTT[-/A]ATTGTTTTTTTCTCC | 8945 |
rs200211669 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463949 | CATCCAGGAAGCTTT[A/T]AAAAAAAAAACAAAC | 8945 |
rs200226579 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101469389 | AATAAAGTCCTATAT[A/T]TAGCCCTACTCTGGA | 8945 |
rs200264479 | in-del | -/CTTTT | 0.0501905 | 0.150254 | intron-variant | BTRC | GRCh38.p7 | 10:101500072 | ATATCTAGTTGCAGA[-/CTTTT]CTTGTGGCCCTACTG | 8945 |
rs200334099 | in-del | -/CC | | | intron-variant | BTRC | GRCh38.p7 | 10:101479215 | TATCTTTGCCCTCCT[-/CC]TTTTCTAACTTACCT | 8945 |
rs200361559 | in-del | -/ATAGATAGATAGATAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101436626 | TTTCAATTAAAAAAA[-/ATAGATAGATAGATAG]ATAGATAGATAGATA | 8945 |
rs200363793 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101439734 | AATAAATGCAGGCTG[G/T]GGGGCAAAGGAGATA | 8945 |
rs200375390 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101509556 | CCGCGCCCAGCCTTT[-/C]TTTTTTTTTTTTTTG | 8945 |
rs200406915 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527358 | TTATACCAAATGCCT[C/G]AGATTTTTATCATTC | 8945 |
rs200450651 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430434 | TAACCCAGGGACTGG[C/T]GCACTCACAGCTTTC | 8945 |
rs200456969 | in-del | -/TTTTG | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101496411 | GTATGACATTTTGGA[-/TTTTG]TTTTAAGTTTTTATT | 8945 |
rs200464364 | in-del | -/A | 0.0221141 | 0.102801 | intron-variant | BTRC | GRCh38.p7 | 10:101549431 | CAAGACTCTGTCTCT[-/A]AAAAAAAATGATGAT | 8945 |
rs200533824 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101389112 | ATAATTGTGATTTTT[-/TG]TGTGTGTTTTTTTTT | 8945 |
rs200563572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432534 | GTTTTTTAACCTTTT[C/T]GGGGTTGCAGTTAGT | 8945 |
rs200567611 | in-del | -/T | 0.0205511 | 0.0992634 | intron-variant | BTRC | GRCh38.p7 | 10:101546404 | ATAAATTGAAATGTA[-/T]TTTTTTTTAATTTTT | 8945 |
rs200568330 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517909 | CTGTTGAAGTAGTGT[C/T]TTTTTTTTTTTTTTT | 8945 |
rs200578010 | snp | A/G/T | 0.000231859 | 0.0107647 | intron-variant | BTRC | GRCh38.p7 | 10:101533111 | AACTCTGAAATATCA[A/G/T]CTCTGCTCTGTTCTT | 8945 |
rs200579215 | in-del | -/GTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101396756 | GGTTTGTTGATGTTT[-/GTT]TTTACATGATGAAAG | 8945 |
rs200601806 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505647 | AAAAAAAAATAATAA[-/T]AAAAAAACAAATATA | 8945 |
rs200619716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463542 | AGTAAAAATAATTCT[A/G]ATTTACTTGGATTTA | 8945 |
rs200644642 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441717 | AAACCCAGTCACTAC[G/T]AAAAATCCAAAAAAT | 8945 |
rs200672536 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532795 | GTGTGTGTGTGCGCG[C/T]GTGCGCGCGCGCGCG | 8945 |
rs200677771 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101418126 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGCAGGT | 8945 |
rs200696452 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101388104 | GATAGAAACCAAAGT[A/G]TGGAGTTACTTCAAA | 8945 |
rs200759313 | snp | A/G | 0.000148267 | 0.00860879 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532983 | CATTGGAATGCAAGC[A/G]AATTCTCACAGGCCA | 8945 |
rs200784936 | snp | A/C | 0.00178447 | 0.029817 | intron-variant | BTRC | GRCh38.p7 | 10:101536682 | CAGAGTGTAAAAAAG[A/C]GAAAATCTACGTCTT | 8945 |
rs200829457 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101355278 | TAGAGGGAAGTAAGT[-/C]CAGGGATAAGTCAGG | 8945 |
rs200829976 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101426862 | TATGGTTAAAAGTGT[C/T]GCCTGCCCTCTTGTG | 8945 |
rs200864138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399925 | TTTTGGATCCTTCTT[G/T]TGAATATGTAACTCT | 8945 |
rs200873141 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407123 | AGCGTTTTAGGAGGC[C/T]GAGGTGGGAGGATCA | 8945 |
rs200882711 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553168 | AGGACCCATTAAAGT[C/T]GCGGTATTTAACGTA | 8945 |
rs200893201 | in-del | -/T | 0.0763149 | 0.179815 | intron-variant | BTRC | GRCh38.p7 | 10:101478449 | TTAGTTTTAAAATAA[-/T]TTTTTTTTTCTGGAT | 8945 |
rs200923762 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101467037 | TATAGTGTGTATTAA[A/C]AAAACAACCACAACA | 8945 |
rs200933026 | in-del | -/CTTGTTGTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101374221 | ACATCCTCTCCAGCA[-/CTTGTTGTTT]CCTGACTTTTTAATG | 8945 |
rs200935913 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101462116 | CAAAACAAAAGACAG[C/G]AGGAAACCCTTGATT | 8945 |
rs200951971 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532814 | CGCGCGCGCGCGCTT[C/T]GCTATACCTATAGAA | 8945 |
rs200952428 | in-del | -/T | 0.02016 | 0.0983543 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556911 | TGCAGTTAAGTCGTA[-/T]TTTAAAGTGTTACCT | 8945 |
rs201012455 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541361 | GCCTCCTGGGTTCAC[A/G/T]CCATTCTCCTGCCTC | 8945 |
rs201045477 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101513736 | TATGGAAGCAAAAAA[A/C]ATTAAAGTACCAGTC | 8945 |
rs201062358 | in-del | -/TCATTCAGCTT | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101424588 | ATTTAGGAGATTTTG[-/TCATTCAGCTT]TCGTATAGTAAATGC | 8945 |
rs201063044 | snp | A/G | 0.000167805 | 0.00915829 | intron-variant | BTRC | GRCh38.p7 | 10:101535335 | CAAATCAACTGCTCA[A/G]TGCCATTTTCTTTTT | 8945 |
rs201068479 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415496 | TTTATTTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs201185248 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101366789 | TATATATATATATAT[-/AT]TTTTACATTTATATA | 8945 |
rs201198184 | in-del | -/CTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101479216 | ATCTTTGCCCTCCTC[-/CTT]TTCTAACTTACCTCT | 8945 |
rs201199406 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101382235 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 8945 |
rs201224727 | snp | C/G/T | 3.61541e-05 | 0.00425159 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521649 | TACAGACAAAACTTG[C/G/T]CAATGGCACTTCCAG | 8945 |
rs201234619 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439656 | AGTTGCCTTAAATGC[A/G]TGAAAAGGGACAGTG | 8945 |
rs201243675 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460297 | CCTTTCCCTTTCTTT[C/G]TTTGATACTCTTACA | 8945 |
rs201257008 | in-del | -/AT | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352557 | CTATTTCTTGAGATG[-/AT]GTCTGCACACGGTTA | 8945 |
rs201281444 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485381 | GCATCAGACTGGCTG[G/T]TTTTAAGCCTGAAGT | 8945 |
rs201335024 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101480994 | ACTAATCCTAGCTCA[A/G]TGCAGCCTTTACCTC | 8945 |
rs201353116 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101396753 | CAGGGTTTGTTGATG[-/TTT]GTTTTTACATGATGA | 8945 |
rs201389963 | in-del | -/TTTG | 0.0599851 | 0.162463 | intron-variant | BTRC | GRCh38.p7 | 10:101482378 | GATCCCTGTTTCTTT[-/TTTG]TTTGTTTGTTTCTTT | 8945 |
rs201398446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486214 | TGTAATCCAATTATA[A/G]CAGCATAAGCAATTT | 8945 |
rs201425647 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488900 | CTTTTCTCATAGGAC[C/T]TTTTTTCACAATATT | 8945 |
rs201426508 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101499003 | GTCTCAAAAAAAAAA[-/A]CAGAAAAAAATAATA | 8945 |
rs201441517 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425644 | TTTTTTTTTTTTTTA[A/T]TTAAAAAAAATGTTT | 8945 |
rs201444608 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496009 | TGGAATCATATAGTA[A/T]TTTTTTTTTTTTACT | 8945 |
rs201456836 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101468211 | AAATTGTGTAATCAC[A/T]GACTTAGTAGGAAAA | 8945 |
rs201490529 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380106 | GTTTAGATTGGTAGG[G/T]AAATTTTACGTTGTA | 8945 |
rs201501194 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495460 | CGTATTGCATTTAAC[C/T]GTGGGCAGCACCAAA | 8945 |
rs201503431 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101372441 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 8945 |
rs201503432 | in-del | -/AT | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101546469 | ATATTTATGGGGAAC[-/AT]GTGATGTTTTGAAAA | 8945 |
rs201503713 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101505628 | CCGTCTCAAAAAAAT[-/A]AAAAAAAAAAAATAA | 8945 |
rs201527753 | in-del | -/T | 0.0700422 | 0.173537 | intron-variant | BTRC | GRCh38.p7 | 10:101543454 | TATAGTTGGGCCATG[-/T]TTTTTTTTTGTTTTT | 8945 |
rs201562154 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101447885 | TTGATTGTTTATCAC[C/T]TTTTTTCTTTAATCA | 8945 |
rs201583958 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101449311 | AAACAAGGATGACAG[-/A]AAAAAAAAAATTCAT | 8945 |
rs201585603 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511297 | ATCTAGAAGGATCTT[C/G]CCCAAGATCTTCACA | 8945 |
rs201586572 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101383397 | ATAAGTCTTCCTTTT[-/TA]AAAAAAAAAAAAAAG | 8945 |
rs201606101 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361113 | GCCCAGCTTTAGCAA[-/T]TTTTTTTTTTTGAGA | 8945 |
rs201618642 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101383398 | TAAGTCTTCCTTTTT[-/A]AAAAAAAAAAAAAAG | 8945 |
rs201647373 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505641 | ATAAAAAAAAAAAAA[A/T]AATAATAAAAAAACA | 8945 |
rs201655998 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543627 | GCTCTTTTTTTTTTC[A/G]TTTTTATCTCAGTTT | 8945 |
rs201696501 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101510519 | CATCTTAAAAAAAAA[A/C]AAAAAAAAAAGTCGT | 8945 |
rs201705390 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543626 | TGCTCTTTTTTTTTT[C/T]TTTTTTATCTCAGTT | 8945 |
rs201728166 | in-del | -/T | 0.0275645 | 0.114116 | intron-variant | BTRC | GRCh38.p7 | 10:101453251 | AAATCGGTCTCAGGA[-/T]TTTTTTCCTTCAGGT | 8945 |
rs201731874 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505634 | AAAAAAATAAAAAAA[-/T]AAAAAATAATAATAA | 8945 |
rs201738490 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420061 | GGGTATATGTGTACA[C/T]ATATATATATATATC | 8945 |
rs201756663 | snp | A/G | 1.66333e-05 | 0.00288381 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531239 | TGTTATTTTTTAGGG[A/G]ACAGTATTTATTCAA | 8945 |
rs201764246 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | BTRC | GRCh38.p7 | 10:101538389 | AAGAGCCTTGCTGTT[C/T]AGAGAGCATTGGAGA | 8945 |
rs201769582 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101491447 | CACTTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 8945 |
rs201804380 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101462895 | ATTTTTGAGACAAAG[C/T]CTCACTCTGTCGCCC | 8945 |
rs201805902 | in-del | -/CCGG | 0.376592 | 0.215579 | intron-variant | BTRC | GRCh38.p7 | 10:101390496 | TGCCCGCCACCACGC[-/CCGG]CTAATTTTTTGTATT | 8945 |
rs201810430 | snp | C/T | 0.293408 | 0.246203 | intron-variant | BTRC | GRCh38.p7 | 10:101467345 | TTTTTTTTTTTTTTT[C/T]CTCTCTATTTGTTTT | 8945 |
rs201814558 | in-del | -/ATATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101366784 | TATATATATATATAT[-/ATATA]TTTTTACATTTATAT | 8945 |
rs201878133 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101395966 | TTTTTTATATGATGG[A/G]AGAAGGTTTTGTATT | 8945 |
rs201913285 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541108 | CTCTTTTTTTTTTTT[C/T]TTAATTGCACTGGCT | 8945 |
rs201965360 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | BTRC | GRCh38.p7 | 10:101497547 | ACAAATAAAAAATAT[-/A]AAAAAAAATTTATCC | 8945 |
rs201971778 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415541 | GTTATGTTATGTTAT[G/T]TTATGTTATGTTATT | 8945 |
rs201982510 | snp | C/G | 9.95636e-05 | 0.00705492 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521862 | GAGATTTCATAACTG[C/G]TCTGCCAGGTATGTC | 8945 |
rs201987537 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101529006 | ATGCTGTCTGCTCAG[C/T]AATGGTAACTCTTAA | 8945 |
rs201991292 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101508787 | GGTGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 8945 |
rs201997979 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550699 | TTTCTACTTCTTTAG[C/G]AGCATTCCGGAAGAG | 8945 |
rs202006499 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505127 | TTTATATATATATAT[A/G]TGTATATATATGTAT | 8945 |
rs202008368 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101463892 | TTTGGATGAACACTT[-/C]TTTTTTTTATAAAAA | 8945 |
rs202032732 | snp | A/C/G | 0.000395331 | 0.0140542 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538361 | GGACACTCTGTCTAC[A/C/G]GACCCTTGTGGTAAG | 8945 |
rs202078725 | in-del | -/TG | 0.0218282 | 0.102165 | intron-variant | BTRC | GRCh38.p7 | 10:101414715 | ATGATCCTTGCTCTC[-/TG]TGTGGGCCTAGGCTA | 8945 |
rs202081619 | snp | C/T | 0.000247331 | 0.0111177 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479417 | AAGAAACAGTATGTT[C/T]AGCAAGCACTGCTAT | 8945 |
rs202110950 | snp | A/C/G/T | 0.000609907 | 0.0174525 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550835 | CCCGTTCCCCTTCTC[A/C/G/T]AACATACACCTACAT | 8945 |
rs202137717 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484154 | TTGTTATTGGTTGTT[G/T]TCACTGTTTTTTTAT | 8945 |
rs202237837 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532786 | TGTGTGTGTGTGTGT[A/G]TGTGCGCGTGTGCGC | 8945 |
rs367558805 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101452958 | ACCTAAGTTTTCCCC[-/C]ATTGTATCCTAAAAG | 8945 |
rs367561962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435247 | TGAGATACATGGATC[A/T]TAAGTGTACTCTTAG | 8945 |
rs367570614 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356659 | CCATTTGAGAAAAGG[C/T]CAACTAGAAGAGGGT | 8945 |
rs367581970 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101444278 | GTTACAATGCCTCCT[A/C]CTGGTTGATCATAGA | 8945 |
rs367589001 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502077 | CAAAGTTACAGGGTA[A/G]TAGAGTTTTTCTGCC | 8945 |
rs367662470 | snp | A/C | 1.65949e-05 | 0.00288048 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531245 | TTTTTAGGGGACAGT[A/C]TTTATTCAAAAACAA | 8945 |
rs367719594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101381545 | GAACTGTAGAATTAG[C/T]ATGCACCTTAGAGTA | 8945 |
rs367747643 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356784 | AAGTCACAACTTCCC[G/T]TTGGTGCCATTTACC | 8945 |
rs367780075 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526567 | GGCAGATCACTCGAG[A/G]CCAGGAGTTTGAGAC | 8945 |
rs367810554 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555952 | CATGCCTTGCTGCAC[A/G]TGTGTGTATTTCACT | 8945 |
rs367830798 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511282 | CTAGCTCTTCCTTCT[A/G]TCTAGAAGGATCTTC | 8945 |
rs367834250 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493183 | TATTTTCACTTGCAC[C/G]GGTAGGTTCTCAAAA | 8945 |
rs367835216 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554420 | TGTTTTTGTTTTTTT[-/T]GTTGTTTTGTTTTGT | 8945 |
rs367842171 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425878 | ATTTAAATATAATTT[A/G]CAAGGAAAAACAACA | 8945 |
rs367858395 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101529339 | ATCAGAAGCTTATGT[A/G]AGTTCTCTTTCCTTA | 8945 |
rs367912215 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550753 | TTCCAGATTGTCAGT[A/T]GTTCACATGATGACA | 8945 |
rs367948471 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363487 | TTTTTGAGATGGAGT[C/T]TTACTCTGTCACCCA | 8945 |
rs367950106 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511496 | ACTCCCAAGTAGCTG[G/T]AACCACATGTGCGCA | 8945 |
rs367963741 | in-del | -/TGTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101505126 | ATTTATATATATATA[-/TGTG]TATATATATGTATAT | 8945 |
rs367973015 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372137 | CAATACCACACTGTC[A/T]TAATTTCTATATTTT | 8945 |
rs367977286 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417649 | ATTTAAGTATCCTCC[C/T]CCTTATCAAACTTAC | 8945 |
rs367978482 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398902 | ACATTGCCTGGTTTT[A/G]CCTGGCTAACCGAAA | 8945 |
rs367983310 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447591 | TCAAACCAATTATCT[A/G]TTACCAAACTCTGTA | 8945 |
rs367984386 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101430799 | ACATAAAGCCAATTA[A/G]TATAATCAATCAATT | 8945 |
rs367992270 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476709 | TCTACCTCCCAAAGT[G/T]CTGGGATTATAGGCA | 8945 |
rs368014752 | in-del | -/GG | | | intron-variant | BTRC | GRCh38.p7 | 10:101485379 | GGCATCAGACTGGCT[-/GG]GTTTTTAAGCCTGAA | 8945 |
rs368042496 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101454805 | CAATCCTTTCAACCC[C/T]GAAATTTCAAGATCA | 8945 |
rs368052088 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497087 | GTTTGATTTTTGTAT[A/G]TGATGCGTGGTAGAG | 8945 |
rs368056603 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521007 | CACAATAGCTCACAC[C/T]TGTTAATCCCAGCAC | 8945 |
rs368060631 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101466788 | ACTGGGCCTTATAAA[A/C]GGAACTACATAAGTC | 8945 |
rs368072770 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482361 | TGTTTTGTGTGTCTC[A/G]TGATCCCTGTTTCTT | 8945 |
rs368073226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406068 | TTCCCTTTAGTTCTG[A/G]GTTTTTTGCTTATTT | 8945 |
rs368089902 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377293 | CCAGACTGTTTATTC[A/G]CTCCTGAAGGACATT | 8945 |
rs368105524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101410876 | GTTATTATTGTCATA[C/T]GTTTTGTTTTCATGT | 8945 |
rs368106208 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101414850 | AATATTTTTGTACTG[A/C]TGTACAATATGTTTG | 8945 |
rs368136075 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101467930 | TAAAGGTAATTAATG[G/T]AGGTCTCTTAAGTAA | 8945 |
rs368147043 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101382222 | TCCCGACCTCAGGTG[A/T]TCCACCTGCCTCAGC | 8945 |
rs368161919 | snp | C/T | 6.60066e-05 | 0.00574447 | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101462010 | AGAAGACTGTAATAA[C/T]GGCGAACCCCCTAGG | 8945 |
rs368182072 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | BTRC | GRCh38.p7 | 10:101534919 | TATAAAGGTAATAAG[A/G]CATTTTTCAGTAAGT | 8945 |
rs368183384 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424958 | TTTACCCCCTTTGTC[C/G]TCCCACCTTTTGTAT | 8945 |
rs368195828 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101396642 | TTCTCATAGCTCATA[A/G]TCATGTTGGTATTGC | 8945 |
rs368203765 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453766 | CATCAAAACATCTTT[A/G]CTTCTTGAATTGGAC | 8945 |
rs368205319 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101455089 | TTCTTTGAGACAGGG[A/T]CTCACTCTGTCGCCC | 8945 |
rs368237270 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428893 | CTGGATTTGAACTCC[C/T]GGGCTCAAGCGATCC | 8945 |
rs368237612 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101464278 | AATTAAACTAAATTT[A/C]TCTCTCTCATACTTC | 8945 |
rs368242513 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536304 | GAACCTGTTTACAGA[A/G]TTATGTAAAGCCCTG | 8945 |
rs368249665 | snp | A/C | 0.000529477 | 0.0162622 | intron-variant | BTRC | GRCh38.p7 | 10:101536513 | GAAAAGAATACGTGA[A/C]AATTCACCTGACTTA | 8945 |
rs368263518 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101440441 | AAAGTTCCTCAATGG[A/C]TGGGCACTGTGGCTC | 8945 |
rs368263680 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431841 | ATATCTTAAGATTTT[C/T]AGTTTTCCTTTACAA | 8945 |
rs368272013 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422359 | TGAGTTCTTTGTAGA[G/T]TCTGGATATTAGCCC | 8945 |
rs368283755 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357349 | GGGAGGCTGAGGCAG[G/T]AGAATCACTTGAACC | 8945 |
rs368299740 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371434 | CGCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 8945 |
rs368305453 | snp | A/T | 0.206029 | 0.246103 | intron-variant | BTRC | GRCh38.p7 | 10:101505635 | AAAAAAATAAAAAAA[A/T]AAAAATAATAATAAA | 8945 |
rs368314946 | snp | A/G | 1.65176e-05 | 0.00287376 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430443 | GACTGGCGCACTCAC[A/G]GCTTTCCAGGTACTT | 8945 |
rs368332122 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377074 | AAAAACTCTTATACT[C/T]TTCCTCCACCTCTAA | 8945 |
rs368353352 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368927 | AGGAGGCTGACGCAC[A/G]AGAATCGCTTGAACC | 8945 |
rs368363424 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454128 | AAAACAAAACAAAAC[C/T]TTTTTTTAAGCTAGC | 8945 |
rs368367455 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386797 | CTGATAGGTGAATTG[A/G]TGGGGGGTGTTTTTA | 8945 |
rs368375218 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489612 | TCAGGAACCATACAT[A/G]CAAAATTTTATTCTT | 8945 |
rs368375946 | in-del | -/AAATGA | | | intron-variant | BTRC | GRCh38.p7 | 10:101358008 | TAAGAAGAGAAATGA[-/AAATGA]TTGAGGGAATATAGA | 8945 |
rs368376311 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101357689 | TGGATACTCTCACAA[A/G]TTTGCTCATTGCTAT | 8945 |
rs368406927 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487369 | GTTGCTGTGGGTATT[A/G]CCACAATAAATACTT | 8945 |
rs368430225 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554311 | TGGTTTCCATCTCCG[A/G]TTTCCTCATCAGGGC | 8945 |
rs368430964 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101539516 | TACATGTTGCTGATG[-/TA]TATCAATATTTCATT | 8945 |
rs368435514 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520819 | AAAACTTAGCCAGGC[A/G]TGGTGGTGGGCACCT | 8945 |
rs368475224 | in-del | -/AG | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101375934 | CCAGTGTATCAACAC[-/AG]GGGAAGTGGGGGAAA | 8945 |
rs368495453 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392922 | ATCCCTTTTTATGGT[C/G]TTTTGTTAATAATGT | 8945 |
rs368554823 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant | BTRC | GRCh38.p7 | 10:101461936 | CTCCCAAAGGATAAG[A/G]TTGAAGATAATGAGA | 8945 |
rs368563308 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415516 | GTTATGTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs368648219 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440472 | ATACCTATAATCTCA[A/G]TACTTTGGGAAGCTG | 8945 |
rs368652064 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401855 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAACAAT | 8945 |
rs368657195 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505304 | CCACCATGCCTGGCC[A/G]TTGACTAATACATTT | 8945 |
rs368671101 | snp | C/T | 3.29592e-05 | 0.00405938 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526115 | GGTACCGAGTGACCT[C/T]TGATGGCATGCTGTG | 8945 |
rs368687642 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101399686 | GTAAATCTGTTAAAA[-/A]TGTTTTACATTAAAA | 8945 |
rs368705039 | in-del | -/TTTTGTTTTTTC | 0.0869089 | 0.189476 | intron-variant | BTRC | GRCh38.p7 | 10:101363457 | CGTTTTTGTTTTTGT[-/TTTTGTTTTTTC]TTTTTTTTGAGATGG | 8945 |
rs368748175 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101434887 | TGATCTGCCCACCTC[A/C/G]GCCTCCTAAAGTCCT | 8945 |
rs368759784 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464519 | TCCCCCTGCCCACTT[C/T]AATTTAACAACCTTC | 8945 |
rs368771357 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101417288 | ATACCTCTTTAGTCT[C/T]GTTTACTCTGGAACA | 8945 |
rs368782794 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363495 | ATGGAGTCTTACTCT[A/G]TCACCCAGGCTGGAG | 8945 |
rs368823905 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394290 | ATGGGATATTTTTAG[A/G]TCTAATTGCCGATGA | 8945 |
rs368875734 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419000 | ATCTCACAGTTTCTT[C/T]TCTTTCTTTCTTTCT | 8945 |
rs368898593 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497841 | CTTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 8945 |
rs368906763 | in-del | -/T | 0.0150935 | 0.0855507 | intron-variant | BTRC | GRCh38.p7 | 10:101459469 | ATGTCCCTACCTCTA[-/T]TTTTTTGTAACAACA | 8945 |
rs368909297 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101412359 | CTGGACAGTACCTTC[G/T]GGTAGAAGACTAGGA | 8945 |
rs368916201 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505132 | ATATATATATGTGTA[C/T]ATATATGTATATATA | 8945 |
rs368921497 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101356105 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 8945 |
rs368946921 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404008 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 8945 |
rs368968037 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378521 | GGCTCCCAATTATAA[-/T]TTTTTTTTTTTTTTT | 8945 |
rs368988151 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421924 | GTGAATAGTGCCACA[A/G]TAAACATACGTGTGC | 8945 |
rs369034048 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101479161 | GCCACTGCTGCTTAC[A/G]TACTTGTTCATGGGC | 8945 |
rs369047909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101419249 | CTCCTGACCTCAGGC[A/G]ATCCACCCACGTCGG | 8945 |
rs369052370 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101491716 | AAAAAAAAAGTCTCT[C/T]AAGGCTTCAGGTCTG | 8945 |
rs369054810 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364835 | TTTTTTTTTTTTTTT[-/G]TATCCCCGGAGCGAG | 8945 |
rs369057688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101513245 | ATAAAATTCATATTA[C/T]AGTGGATTTATCAGT | 8945 |
rs369127682 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496733 | TTTATGTTGATTGGC[C/T]ATTTGGATGTGAAGT | 8945 |
rs369140718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518979 | ACATAGTGGCTGGGT[G/T]CTCTGCTGAGAGCAT | 8945 |
rs369141587 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101508938 | AAAAAAAAAAAAAAC[A/T]AAAAGTAGAATGTTA | 8945 |
rs369142766 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528614 | ATACATCCCGTGTCA[A/G]CTTCCTCCATTATTC | 8945 |
rs369145401 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363528 | CAGTAGCGCAATCTC[A/G]GCTCACTGCCACCTC | 8945 |
rs369176528 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453355 | CACAATTTACCTGCT[G/T]TGCTAAAATGATAGA | 8945 |
rs369196107 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101549530 | CCATCCTGGCTAACA[C/G]GATGAAACCCCGTCT | 8945 |
rs369213720 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101512705 | ATTTTGAAAGTGGTA[C/T]GTGAAATATGTTTTC | 8945 |
rs369225512 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458031 | AGTTACAGACGTAAT[A/G]TTCCATCCCCCCTAA | 8945 |
rs369237443 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411245 | GAAATCTACCTGCCT[C/T]GGCCTCCCAAAGTGC | 8945 |
rs369240383 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101478529 | AGCACAATGGCTCGT[A/C]CCTGTAATCCCAGCA | 8945 |
rs369249292 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489855 | CATCTTTTTTTGTTT[A/G]TACTGTAATCCCAAA | 8945 |
rs369257810 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435032 | ATGTCAGGTTCAGCA[C/G]ACACAGGTGCTTGAT | 8945 |
rs369292115 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451903 | ACCAGCGAATAAAAT[C/G]AGCCATTCATGTGAG | 8945 |
rs369302559 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472914 | TCAGCAGTTCTGACT[A/G]TGATGGGCCTATATG | 8945 |
rs369305273 | in-del | -/ATATATAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101475923 | TCCAAGTATTTTGCC[-/ATATATAT]ATATATATATATATA | 8945 |
rs369319104 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541539 | TGCTGGGATTACAGG[C/T]GTGAACCACCGCGCC | 8945 |
rs369328041 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101529924 | CTCTCTCCACTTTGC[A/G]AGGCACGGTGCCAGT | 8945 |
rs369335517 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101390517 | TTTTTGTATTTTAGT[A/G]GAGACGGGGTTTCAC | 8945 |
rs369389329 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398542 | TCTCCTGACCTCGTG[A/T]TCTGCCTGCCTTGAC | 8945 |
rs369406818 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415531 | GTTATGTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs369412287 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465726 | AACAAGAAATAATGA[A/G]GGTGGAAATTAAGAG | 8945 |
rs369414731 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423881 | CATTCACAGAAGCCT[A/G]TTCCTGGTGATGATG | 8945 |
rs369443360 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101384785 | GAAGTAAAATACATT[C/G]TAGTTAAAAATTGAG | 8945 |
rs369451711 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440713 | GGTTGACAGAGTGAG[A/G]CTCCATCTAAAAAAG | 8945 |
rs369480461 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499180 | AACTAACTTGTTCAG[A/G]TCTATATAGCTTGTA | 8945 |
rs369482489 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453687 | AGATAACTGAAAATA[A/G]TAAATAAGCCACTTA | 8945 |
rs369494639 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101391122 | TCTTTTAAAACAACT[G/T]GTACAGGTTACTATT | 8945 |
rs369532778 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541847 | ATATCTTTTTAAGGA[G/T]TTTTGTGTGTGTGTG | 8945 |
rs369604790 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554395 | AAGAGAGATGGTCAG[A/G]AGAAAACACTGTTTT | 8945 |
rs369616437 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497221 | TATAGGTCTTTATCA[A/G]AATCTTGAACTCTGA | 8945 |
rs369641092 | snp | C/T | 3.29766e-05 | 0.00406045 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479408 | GCTTAAACCAAGAAA[C/T]AGTATGTTTAGCAAG | 8945 |
rs369643602 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101545575 | GGTGTCCTTAAAACA[A/C]GAGGAGATTGGGACA | 8945 |
rs369664084 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377470 | CTATTTTCCAGAGTG[A/G]TTGTACCAGTTGGCA | 8945 |
rs369675705 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389058 | TTTACTGTGACTTCT[A/G]CCTTTATGTATTCAA | 8945 |
rs369679821 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101420639 | GGTCCCCCTCCCAGC[A/G]GATTTTTTCCTATCA | 8945 |
rs369719199 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492657 | AGATTGAAGGCGTTT[C/T]CTTTAACCCTTTCTT | 8945 |
rs369719640 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406036 | TTAGGCTCTCAAACT[-/AT]GTAGATTTGTGTATT | 8945 |
rs369741351 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504264 | GGTTTTAAAAAATAG[-/T]TTTTTTATCTCCTCT | 8945 |
rs369767372 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101534282 | GTATGTGACAGAAGC[A/G]TCTTGGCCTATTTCA | 8945 |
rs369777460 | snp | A/G | 3.31131e-05 | 0.00406884 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521857 | GCAGAGAGATTTCAT[A/G]ACTGCTCTGCCAGGT | 8945 |
rs369794525 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363517 | AGGCTGGAGTGCAGT[A/G]GCGCAATCTCAGCTC | 8945 |
rs369804931 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101484130 | CTTTGTGGATGTTCT[A/G]TATTTTAGTTGTTAT | 8945 |
rs369821979 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436673 | ATAGATAGATAGATT[G/T]ATATGGCCCTAGAAT | 8945 |
rs369824717 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101372028 | GATTGTTCTTTTTCT[A/G]TTGCAGGGTCATTTT | 8945 |
rs369835345 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101429134 | CCTATATTGACTACT[A/G]TATTTTAAAATATGT | 8945 |
rs369863334 | in-del | -/TA | 0.499958 | 0.00459246 | intron-variant | BTRC | GRCh38.p7 | 10:101366830 | ATATTAATATATATT[-/TA]TATATATATTTATGT | 8945 |
rs369869740 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101550979 | ATGGAACTTTCTCCT[C/G]CCGTTTGGGTCACCA | 8945 |
rs369876192 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366472 | AGAATTTAAGAGAGG[C/T]GACAGGAAAAAAAAG | 8945 |
rs369882539 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101394000 | TAAAACTGAGTGTAT[A/T]ATTGAGTCTGTACCT | 8945 |
rs369883261 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424274 | TTAGTTTTACCACAA[A/C]CTTGTGCAATAAGGC | 8945 |
rs369894484 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354145 | GCACCAAAGGGGCGG[C/T]CCCGGCGGAGAGCGG | 8945 |
rs369924525 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493675 | ATGATAGAGTAATAC[A/G]TCTTAGGTTTGTTTT | 8945 |
rs369928321 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506056 | TTAGCTGGGACTACC[A/G]GTGCCGGCCACCATG | 8945 |
rs369934484 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459084 | GGATTACACGCATAT[A/G]CCAAAGTACTAGGCT | 8945 |
rs369946021 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538641 | TAGTGCAGGGAGTGA[A/G]TAAGAATTCTGTATC | 8945 |
rs369946455 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101524535 | TAAACCAAACTACTT[C/T]AAAAAGTGCCTGTAG | 8945 |
rs369951511 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403033 | AGATTATAACCTCTT[C/T]AAAAGCAGGGACTCA | 8945 |
rs369979857 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422041 | AGATCCCTGAGGAAT[C/T]GCCACACTGTCTTCC | 8945 |
rs370002334 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472643 | AATATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8945 |
rs370003852 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444775 | TGAAAACAAAAAATC[C/T]GAAGGAGATAAATTA | 8945 |
rs370049325 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101390411 | GGTGCAATCTCTGCT[A/C]ACTGCAAGCTTCGCC | 8945 |
rs370051607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360209 | ACAGGCATGTGCCAC[A/C]ACGCCCAGCTAAATT | 8945 |
rs370123208 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441651 | GTGGGAGGCTGAGGC[A/G]GGCGGATTGCCTGAG | 8945 |
rs370128933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396465 | TGCCCAGGCTGGTCT[C/T]GAGCGAGGTAAAGAT | 8945 |
rs370144751 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441085 | TCAGTGGGGGAGTTT[-/T]CAAAAATCATTCTTG | 8945 |
rs370144923 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366972 | TATTTATATAAATAT[A/T]TATTTATATATTTAT | 8945 |
rs370161763 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101375273 | CCTTCTCTGCCCCCC[G/T]CTCTTCCCCCCTTCT | 8945 |
rs370161905 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407426 | TTATTTTTGTTTTTA[G/T]TTCTTTGGAAACAGT | 8945 |
rs370191694 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410059 | GTTCCAGTTTCTCCA[C/G]ATCCTTGTCAGCACT | 8945 |
rs370200871 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511472 | GTTCAAGCAGTTCTC[A/G]TGCCTCAGACTCCCA | 8945 |
rs370201424 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101522404 | AACTCTAGAAATAAA[A/G]ACTCCTTTTTTTTTT | 8945 |
rs370204207 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525173 | ATAGGATCTTTTCTT[C/T]TGAGACCTCAGTACA | 8945 |
rs370207221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542483 | GTGATTTTTCTATTC[A/G]TCCTTACCAATTATT | 8945 |
rs370212588 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534746 | CGTTTCAATAATGGC[A/G]TGATGGTGACCTGCT | 8945 |
rs370214089 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101537798 | TTGGTCAAGACAATA[A/T]TTTCTTATTGTCCTG | 8945 |
rs370270249 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403547 | AGTTTAAAAATTTTA[G/T]TTTCAGTTTTCTCAT | 8945 |
rs370273573 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101367224 | TACATGCGCGCACCA[C/G]CACGCCAGCTAATTT | 8945 |
rs370296657 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463493 | CCCTGTATTCATTTT[C/T]AATATAAAATTGGAT | 8945 |
rs370314604 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502729 | CAATACCCACCTCCT[C/T]GTTCATTTAGATTAA | 8945 |
rs370318359 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101439501 | GTTGCAGTATCGTTG[C/T]ACATTCCTTGTATTG | 8945 |
rs370340979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451453 | GAAAGGCAGCCATCT[A/G]TCTAGGGAGTTCTTC | 8945 |
rs370353886 | in-del | -/TTTTT | 0.351418 | 0.228505 | intron-variant | BTRC | GRCh38.p7 | 10:101383058 | GGCCTTCCCTGGAGA[-/TTTTT]TTTTTTTTTTTTTTT | 8945 |
rs370389340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531700 | CACTCCCTCCTGAAC[A/G]ACAGAGCGAGACTCC | 8945 |
rs370409705 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422272 | CATAAATGTCTTCTT[C/T]TGAGAAGTGTCTGTT | 8945 |
rs370453446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101467106 | CATACTGTATTTCTG[C/T]TCTTTGGAGGACAAT | 8945 |
rs370471673 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | BTRC | GRCh38.p7 | 10:101430319 | GTCTCATACTGTCCC[A/G]TCTCATAGTTGTCCT | 8945 |
rs370472183 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367051 | ATATATAAATATATA[-/T]ATATATAAATATAAA | 8945 |
rs370478784 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489555 | GCTTACAAAGCTTGT[A/G]AAACCTGAGCCTTCC | 8945 |
rs370491574 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520615 | ACCACAGAGTCTCAG[A/G/T]ATATTCATTGGTTTC | 8945 |
rs370494099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101408002 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 8945 |
rs370509457 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101440902 | TAAGTCCTGCTCCTT[C/T]GTAGCCAGATTTTTG | 8945 |
rs370536242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378341 | TGTTTTTCACATTTG[A/G]AATGCATACTTGCTG | 8945 |
rs370541699 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421824 | TTTTATGGCTGGCTA[C/G]TATTCCATGGTGTAT | 8945 |
rs370545555 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555641 | ACTTACCATCTCTGC[A/C]TGATTTCAGTGGGAA | 8945 |
rs370558446 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464031 | TGTTTGGAGAATCAA[C/T]ACCTGATCTGTTCAT | 8945 |
rs370570566 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101375283 | CCCCCTCTCTTCCCC[C/G]CTTCTCTTCTTCCTG | 8945 |
rs370575359 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101449997 | AGCAGGATAAAAATG[A/T]AAAAAAAAAAAACTA | 8945 |
rs370611925 | snp | A/G | 1.65518e-05 | 0.00287674 | intron-variant | BTRC | GRCh38.p7 | 10:101533107 | TTTGAACTCTGAAAT[A/G]TCAGCTCTGCTCTGT | 8945 |
rs370616807 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101447884 | CTTGATTGTTTATCA[A/C]TTTTTTTCTTTAATC | 8945 |
rs370660495 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363481 | TTCTTTTTTTTGAGA[C/T]GGAGTCTTACTCTGT | 8945 |
rs370662030 | snp | A/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405544 | CCACTTGTGGGTTTC[A/T]GGCAGCAGTCCAGGC | 8945 |
rs370701476 | in-del | -/AAAG | 0.115788 | 0.21092 | intron-variant | BTRC | GRCh38.p7 | 10:101390766 | TTTGTTTGTCTTAAA[-/AAAG]AAAGAAAGAAAGAAA | 8945 |
rs370702894 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101509428 | CCCGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 8945 |
rs370774496 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101383986 | TCCCAAATAGTTGCC[-/G]GGTACCACAGGCTTG | 8945 |
rs370785248 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506816 | TTCACAAAGGGTTAA[A/G]TTATGTAGTTAGTGA | 8945 |
rs370831952 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486118 | GAAAGAGAGAGGCAA[C/G]GCAAATAAAATTACT | 8945 |
rs370862535 | snp | A/G | 7.47077e-05 | 0.00611132 | intron-variant | BTRC | GRCh38.p7 | 10:101521909 | CCATTAATTTGCTAT[A/G]ATGATAAGAGAACTA | 8945 |
rs370874740 | snp | A/G | | | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354465 | GCCAAGTGACAGCGG[A/G]AGCTTAATCGAGGAG | 8945 |
rs370875449 | snp | C/T | 3.30633e-05 | 0.00406578 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526049 | CTGAGAACATTCTGT[C/T]ATACCTGGATGCCAA | 8945 |
rs370893133 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101443073 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 8945 |
rs370899708 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101534132 | ATATTTACAATGGGG[G/T]GTCTATTTTAAACCC | 8945 |
rs370903185 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101509797 | AGACTCCTGGGTTCA[A/G]GCAGTCCTTCTGCCC | 8945 |
rs370907792 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | BTRC | GRCh38.p7 | 10:101518114 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 8945 |
rs370914044 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483585 | GCGACAGAGTGAGAC[C/T]CAGTCTCAAAAAAAA | 8945 |
rs370921512 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539773 | TTCAAAGTGGTTTAC[C/G]CTTTTACATTATAGT | 8945 |
rs371000178 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526165 | ATGGTCAGGACAGAT[C/T]CTCTGTGGAGAGGCC | 8945 |
rs371006666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378849 | CCATGGGAAAACATC[C/T]GCTTTGAAGCAGTAT | 8945 |
rs371019287 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525249 | CACTCCCCAAGATCT[A/G]TTCTCCACTGTTTTC | 8945 |
rs371027551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536280 | TTGAATTCGTTTTTA[C/T]GCCTGGAAGAACCTG | 8945 |
rs371028514 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101371234 | CTGTTGCCCAGACTG[C/G]AGTGCAATGAATGGC | 8945 |
rs371037950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548211 | AACATACACCTACCC[C/T]GTGGCCCAGCAAGTC | 8945 |
rs371045091 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101426767 | TAATTTTAAAAAGAG[C/T]CCCAAGTCTGTGAAT | 8945 |
rs371049035 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101461229 | TTTAAATATTAATGT[A/T]ATTAATGTTACTAAT | 8945 |
rs371060165 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488996 | CTGCATTTACAGAAA[C/T]TTAAGTCTCTAATAT | 8945 |
rs371065443 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396755 | GGGTTTGTTGATGTT[G/T]GTTTTTACATGATGA | 8945 |
rs371074380 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501069 | GGCATGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 8945 |
rs371082162 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101537211 | GGACCCCATGTCCAC[A/C]AATCCTAAACACAGA | 8945 |
rs371099958 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505129 | TATATATATATATGT[A/G]TATATATATGTATAT | 8945 |
rs371106970 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366790 | TATATATATATATAT[A/T]TTTACATTTATATAT | 8945 |
rs371119572 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101429775 | TTTGGTTAATGAATA[A/G]CAGACTAACAAGATA | 8945 |
rs371119833 | snp | C/T | 4.95094e-05 | 0.00497517 | intron-variant | BTRC | GRCh38.p7 | 10:101534645 | GTACCATCTAAATCT[C/T]ATCTATCACTTCCAG | 8945 |
rs371128169 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370511 | GACAAAATGAGTAGA[A/G]GTTTATTGTAGTCAA | 8945 |
rs371133214 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474205 | CATTATAAATGGTAC[A/G]TTGCAGAAACTCTGA | 8945 |
rs371193133 | in-del | -/GTTTTTTCTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101363461 | TTTGTTTTTGTTTTT[-/GTTTTTTCTTTT]TTTTGAGATGGAGTC | 8945 |
rs371239961 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101399912 | TCAGAAATACTCATT[A/T]TGGATCCTTCTTGTG | 8945 |
rs371251368 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367006 | TATTAATATATATAT[A/T]TATATATATATTTAT | 8945 |
rs371311444 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551260 | AAACAATACCTACAA[-/T]AGAGACCTTTCAAGC | 8945 |
rs371321893 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101478318 | AAAAAAAAAAAATAG[A/G]TAAGTGTTGGTTTAT | 8945 |
rs371326688 | in-del | -/GTGT | | | intron-variant | BTRC | GRCh38.p7 | 10:101532794 | TGTGTGTGTGTGCGC[-/GTGT]GCGCGCGCGCGCGCT | 8945 |
rs371331889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101395152 | GGGGAGTTGAGGCCT[C/T]ACACAGAGGGATTTT | 8945 |
rs371336032 | snp | C/G | 1.65526e-05 | 0.00287681 | intron-variant | BTRC | GRCh38.p7 | 10:101461948 | AAGATTGAAGATAAT[C/G]AGAACTGAATTAAAG | 8945 |
rs371337656 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425988 | AAATGTTGAAGGACA[A/G]AAAACATCTTACATA | 8945 |
rs371345488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101404854 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 8945 |
rs371349417 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101438298 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 8945 |
rs371350901 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363252 | CTCAAAGTCATGCTA[C/G]CAGGTATCCTGAGAT | 8945 |
rs371371262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457820 | TATTATGGATTTAAT[A/T]AATTAATTTTTTATT | 8945 |
rs371372703 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520844 | GCACCTGTAGTCCCA[A/G]TACTTGGGAGGCTGA | 8945 |
rs371397746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450288 | CCCCTCCCTTTTTTG[A/G]TCCCCATATTTATTG | 8945 |
rs371411500 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544670 | CTCACAACCTCCTGA[A/G]TAGCTGAGATTATTA | 8945 |
rs371420237 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363490 | TTGAGATGGAGTCTT[A/G]CTCTGTCACCCAGGC | 8945 |
rs371432679 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536565 | GACATAGAATGTGGT[A/G]CATGTTTACGAGTGT | 8945 |
rs371459043 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489810 | TGTTTCTTAAGATTA[A/G]CATTAAAATAGACAT | 8945 |
rs371468250 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101375195 | TGGGGGCGGATTTCC[A/G]CCTTTTGTGCTGTTT | 8945 |
rs371496371 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358718 | TGCTTGGATTTCCTT[A/T]AAGTGTGGTGGCAAG | 8945 |
rs371532181 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463065 | GTTTTTTTTTTTTTG[A/G]GACACAGTCTTGCTC | 8945 |
rs371544527 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101365569 | CAACCTCTGCCTTCC[A/G]GGTTCAAGCAATTCT | 8945 |
rs371551089 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398293 | ATGTGTGTTGAAAAT[A/T]TCTTTTTTTCTTTTT | 8945 |
rs371553568 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414800 | TATAATATATATTTT[G/T]TAAATAGGAAACAAC | 8945 |
rs371601146 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101357124 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAACAAA | 8945 |
rs371609962 | snp | C/T | 9.96727e-05 | 0.00705878 | intron-variant | BTRC | GRCh38.p7 | 10:101430466 | AGGTACTTTCTCTGT[C/T]TCTGTGGGTTATTTG | 8945 |
rs371635822 | snp | A/G | 5.12194e-05 | 0.00506035 | intron-variant | BTRC | GRCh38.p7 | 10:101479329 | TATGGCAGTATTTCA[A/G]TATTTTAAAAACCTG | 8945 |
rs371657425 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353634 | CCAGATACATGAAAT[C/T]TGGGGACGTTCAGCT | 8945 |
rs371668151 | in-del | -/ACAC | | | intron-variant | BTRC | GRCh38.p7 | 10:101505126 | TTTATATATATATAT[-/ACAC]GTGTATATATATGTA | 8945 |
rs371675689 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518846 | GAAATGATCTCTAAC[C/G]ACTTAAATAATCCTA | 8945 |
rs371692654 | snp | C/T | 0.00013242 | 0.00813586 | synonymous-codon, intron-variant | BTRC | GRCh38.p7 | 10:101531270 | AAACAAACCTCCTGA[C/T]GGGAATGCTCCTCCC | 8945 |
rs371717504 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101513596 | TCATCTTTACCATTT[A/T]GTGTGTCTGTGGTTT | 8945 |
rs371755500 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536759 | CTAAAAGCTTATAGA[C/T]TTTACACAAAATATC | 8945 |
rs371758415 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101537870 | GTACCTTGAGGAAAC[A/G]TGGCCTATTAAAAGA | 8945 |
rs371762627 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101551762 | TCCTCAGCTTCTCTT[C/T]CTCTCACAGAGGACA | 8945 |
rs371790376 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101356060 | GTCTTGCTTTGTCGC[C/T]CAGGCTGGAGTGCAG | 8945 |
rs371801079 | in-del | -/GTGT | | | intron-variant | BTRC | GRCh38.p7 | 10:101431032 | GAGACACTCTAGCTA[-/GTGT]GTGTTTCATGAATTA | 8945 |
rs371823953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377179 | TTACTGACCTCTTCC[A/G]TTCAGCATAATGCCT | 8945 |
rs371837513 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101532575 | TCCCAAAGCCAAAAT[A/C]ATTTCCTTAAAGGAC | 8945 |
rs371848400 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475426 | ATGTCTGTAATCCCA[A/G]CTACTTGGTAGGCTG | 8945 |
rs371854583 | in-del | -/GA | | | intron-variant | BTRC | GRCh38.p7 | 10:101527360 | TACCAAATGCCTCAG[-/GA]AKWTTTATCATTCTG | 8945 |
rs371856353 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101417907 | GGTCTCTAATTCTTG[A/G]CCTCAGGCAATCTGC | 8945 |
rs371867459 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516523 | AAAAAATACTCGTTT[C/T]GAGGGGTGGTGACTA | 8945 |
rs371878622 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101362412 | AATTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 8945 |
rs371909874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101405120 | TTTTCTTGAGTTCCT[A/C]CCTCTGTACAATCTC | 8945 |
rs371932644 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422900 | TTTGAAGTCAGGTAG[C/T]ATGATGCCTCCAGCT | 8945 |
rs371933661 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423483 | TATAGTAGCTGTTGT[C/G]TAATGCAATTTAGTA | 8945 |
rs371940150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537025 | GTATTTGGGGACTTA[A/G]TGTGGTAAGATCTTG | 8945 |
rs371945681 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101508201 | AAATAGGAAAAAAAG[A/G]TTGGCAAGTGTCCAG | 8945 |
rs371963882 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469117 | AACTCTCTGCCTCTG[A/G]TTCAGCAATGAAGCT | 8945 |
rs371976751 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101489111 | AGGATTCTGTTAGAA[C/T]AGAAATCTGATTTTT | 8945 |
rs371989418 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101437190 | ACCCTTCACCTTAGG[G/T]GTTTGCAGGGAATGA | 8945 |
rs371993968 | snp | C/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406219 | TCTCGCTCTGTCTCC[C/G]AGGCTGGAGTGCAGT | 8945 |
rs371999396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447567 | ATTAAAATTAATGTT[G/T]GATATCTGTCAAACC | 8945 |
rs372035766 | snp | C/G | 1.69115e-05 | 0.00290782 | intron-variant | BTRC | GRCh38.p7 | 10:101535316 | ATTTTACCAATAAAA[C/G]CACCAAATCAACTGC | 8945 |
rs372040886 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101537725 | TCTTCTGCTTTGGGA[-/C]CAGCCATCACTGTTA | 8945 |
rs372051392 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361169 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG | 8945 |
rs372090923 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101477201 | AGACGGGGTTTCACC[A/C]TGTTGGTCAGGCTGG | 8945 |
rs372097627 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362413 | AATTTTTTTTTTTTT[G/T]AGATGGAGTTTCGCT | 8945 |
rs372111877 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392835 | GACCAATTAAAAGTT[G/T]TAATATTCCCCCTGT | 8945 |
rs372131848 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421885 | ATTGTTGGACATTTG[G/T]GTTGGTTCCAAGTCT | 8945 |
rs372144138 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101443535 | CTGTTGGTTACCATT[C/T]TGAGCATTTAAAACG | 8945 |
rs372145262 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101393030 | ACTCTAATCTCCCAC[C/G]ACCTCCTTTCTGATT | 8945 |
rs372149213 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512145 | CAATAAACTGTTGTT[A/G]GTTGATTGATACCAC | 8945 |
rs372181043 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101487771 | GATCAACCTTTTAAT[C/T]AGCAAGAGTGGAAAC | 8945 |
rs372192342 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363501 | TCTTACTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 8945 |
rs372221464 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427598 | AGTGGCATGATCACC[A/G]CTCATTGCTGCCCTG | 8945 |
rs372236414 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411034 | ACAGTGTCACTCTGT[C/T]GCCCAGGCTAAAGTG | 8945 |
rs372240094 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415491 | TTTATTTTATTTTAT[-/G]TTATGTTATGTTATG | 8945 |
rs372242067 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397079 | AAAGTGCTGAGATTA[C/T]AGGCATGAGCCACTG | 8945 |
rs372264785 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368272 | ATGCAGCTCCTCTTC[A/G]CCCTCCACCGTGAGT | 8945 |
rs372275322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545388 | CCTTAAAAGTAAATG[A/G]TTAGCGAAAGATATA | 8945 |
rs372280258 | snp | G/T | 3.3094e-05 | 0.00406766 | intron-variant | BTRC | GRCh38.p7 | 10:101536516 | AAGAATACGTGAAAA[G/T]TCACCTGACTTAATT | 8945 |
rs372290558 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505637 | AAAAATAAAAAAAAA[A/T]AAATAATAATAAAAA | 8945 |
rs372290992 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505134 | ATATATATGTGTATA[C/T]ATATGTATATATATA | 8945 |
rs372309900 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515602 | CTGCAATCTCCACCT[C/T]CCGGGTTCAAGTGAT | 8945 |
rs372313990 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101503400 | TTCAGCTTATATAAT[A/T]ACTGCATTTTGAAAT | 8945 |
rs372332947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544272 | ACGTTTACCTTTTCT[A/G]TTGCCTCCCATTCCT | 8945 |
rs372344159 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556905 | GATCAGTGCAGTTAA[A/G]TCGTATTTTAAAGTG | 8945 |
rs372360054 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101361165 | AAGCTGGAGTGCAGT[C/G]GTGCGATCTCAGCTC | 8945 |
rs372376670 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101483316 | AAAACTAAAAATGGC[C/T]GGGCACGGTGGCTCA | 8945 |
rs372408026 | snp | C/T | 8.24382e-05 | 0.00641968 | stop-gained, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550834 | CCCCGTTCCCCTTCT[C/T]GAACATACACCTACA | 8945 |
rs372413571 | snp | C/T | 1.65307e-05 | 0.0028749 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532375 | AAGCAAAGGAGTTTA[C/T]TGTTTACAGTATGAT | 8945 |
rs372468526 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357566 | TTGGCTTTGTTCTGG[C/T]CTTAACCTTTCCCTC | 8945 |
rs372492937 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428172 | GGGAGAAGGAAATTA[C/T]AAGTTTAAAGACAGG | 8945 |
rs372502893 | snp | A/G/T | 0.0130921 | 0.0798413 | intron-variant | BTRC | GRCh38.p7 | 10:101422205 | GTGGTTTTGATTTGC[A/G/T]TTTCTCTGATGGCCA | 8945 |
rs372503735 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472612 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 8945 |
rs372508214 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461112 | TCAGCATGTTGGCCA[A/G]GCTGGTCTCAAACTC | 8945 |
rs372517079 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370045 | TGCTTTTCACATCAC[A/G]TTTGGACTTCAACAC | 8945 |
rs372553291 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101366782 | TATATATATATATAT[-/A]TATATATTTTTACAT | 8945 |
rs372559788 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415521 | GTTATGTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs372587156 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408903 | AATACAAAAAAATTA[C/G]CTGGGCGTGGTGGTG | 8945 |
rs372591426 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101427488 | TTTTTTGAGACGGGT[C/T]CCTTCCTTCCTTCCT | 8945 |
rs372607322 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101496609 | AATATAAAATTTACC[A/G]TCTTACTATTTTTAA | 8945 |
rs372618388 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504548 | TCACCAACCCCACTG[C/T]CTAGTATCCACTGTC | 8945 |
rs372626284 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451569 | TTAAAGCAGTAGTGT[A/G]TTTTAAGAATGTGTG | 8945 |
rs372649029 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377623 | TTTGTATTTCCCTAA[G/T]GCATTCCTCGATTCT | 8945 |
rs372653996 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101469421 | ACTCCCTCAGGCCTG[A/G]CACAGAGTTTCTGAA | 8945 |
rs372659297 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449150 | TTGGGATGGTTTTAC[A/G]TCTCGGGATATTAGC | 8945 |
rs372671071 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354127 | TGCGTTGGCTGCGGC[C/T]TGGCACCAAAGGGGC | 8945 |
rs372691225 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433138 | CCATTCCTTTCTTTG[A/G]TGAAGAGTAATTCTT | 8945 |
rs372736036 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389982 | CCAACTCTGACTTTT[C/T]GGTTGAGTCCTTCGT | 8945 |
rs372747349 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101416053 | CACAGCCGAGAAATC[A/C]CCTAGTGATGCATTT | 8945 |
rs372782061 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101384501 | TATGAGTAGTTTATG[A/G]TAAATTATAGTTCTA | 8945 |
rs372787240 | snp | A/T | 0.000757442 | 0.019446 | intron-variant | BTRC | GRCh38.p7 | 10:101550910 | TCGAAATCGATTATG[A/T]ACATAACACTGTGGG | 8945 |
rs372796056 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530038 | TTAAATTTTTTACCC[A/G]GCAGGAAGTGATTGC | 8945 |
rs372819628 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502373 | AACATTGTAGCAATA[G/T]CTCTGAAAGATTGAA | 8945 |
rs372833367 | snp | A/G | 0.000923126 | 0.0214642 | intron-variant | BTRC | GRCh38.p7 | 10:101521913 | TAATTTGCTATGATG[A/G]TAAGAGAACTAGATC | 8945 |
rs372864623 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101371524 | TAGATACCTCATTTA[A/C]GTAGAATCATACAGT | 8945 |
rs372873543 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481560 | CTATATGATGTGGAG[-/T]TTTTTTTTTTTTAAT | 8945 |
rs372886221 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365298 | GGCTGGTCTTGAACT[C/T]CGGATCTCAGGTGAT | 8945 |
rs372912956 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101548967 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 8945 |
rs372918479 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445054 | GTAGAAACTCGATAT[A/G]TTAGGGTTTAGTTAT | 8945 |
rs372951748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101504230 | TAAACTTTATTACTC[C/T]GCCTGAAACATTAAG | 8945 |
rs372991368 | snp | A/G | 9.94662e-05 | 0.00705147 | intron-variant | BTRC | GRCh38.p7 | 10:101536693 | AAAGAGAAAATCTAC[A/G]TCTTAATCCTTCCTT | 8945 |
rs373000514 | snp | G/T | 4.95831e-05 | 0.00497886 | intron-variant | BTRC | GRCh38.p7 | 10:101533089 | GAAAATTTCAAATGC[G/T]TTTTTGAACTCTGAA | 8945 |
rs373015627 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445434 | GCTTCTGTTTAAATC[A/G]GTAGAAAATATGTTG | 8945 |
rs373017360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381686 | GAAAAATTATGAGAA[A/G]CACACGATGATAACT | 8945 |
rs373029887 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532621 | CACTATACAAACGGG[C/T]AGTCCTAGGGTTAAA | 8945 |
rs373041165 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545622 | AGATAAAGGGAGAAG[A/G]TGACCATCTACAAGT | 8945 |
rs373042921 | snp | C/T | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557721 | CTGTAAGAATGAAGG[C/T]ACCCTTGACTATCTG | 8945 |
rs373067576 | in-del | -/GTT | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353048 | GTTGTTGTTGTTGTT[-/GTT]ATACTGTTCTTTTTC | 8945 |
rs373072689 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101363522 | GGAGTGCAGTAGCGC[A/C]ATCTCAGCTCACTGC | 8945 |
rs373086985 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517261 | AAATGGCCTAATGCC[A/G]TTCTTGAAAATATGC | 8945 |
rs373096046 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518062 | GGACTACAGGCGCCC[A/G]CCACTACGCCCGGCT | 8945 |
rs373104717 | snp | A/G | 9.88386e-05 | 0.00702919 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534697 | TGAAATGCTAAACAC[A/G]TTGATTCACCATTGT | 8945 |
rs373141707 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554080 | GGGGGTGGGGAGAAG[C/T]TTCCTGGGCTCCATC | 8945 |
rs373158614 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101480736 | ATAACCATCGAAATC[-/AT]ACATATAAGAAATAT | 8945 |
rs373178651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383648 | GGGGTTACAGGCATG[A/G]GCCACTGTGCTGACC | 8945 |
rs373199154 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474133 | ATTTTTCTCTTGACA[A/G]TGGATCCCATTTATC | 8945 |
rs373224128 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360681 | TGGCCTCTAGAGATG[A/G]GATCTTGCTTGCTCT | 8945 |
rs373235991 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101444681 | CTTAAAAAGAATACA[A/G]TTACAAATAGCACCC | 8945 |
rs373241616 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469664 | TAATTGTATAAGTCT[C/G]AATTTTTGATAAATC | 8945 |
rs373242605 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101492014 | AATGGAAAGGTTAGA[A/C]ATGCTTGACAGTTAA | 8945 |
rs373252202 | snp | C/G | 0.000182196 | 0.00954279 | intron-variant | BTRC | GRCh38.p7 | 10:101533109 | TGAACTCTGAAATAT[C/G]AGCTCTGCTCTGTTC | 8945 |
rs373264156 | in-del | -/AA/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101366860 | ATATTAATATATATT[-/AA/TA]TATATATTAATATAT | 8945 |
rs373268187 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423054 | CCATGAGTTTTTTTT[A/G]ATTAAGTTAAATTTT | 8945 |
rs373340953 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369252 | AGATGGGTTCTTGCC[C/T]TCTTGTCCAGGCTCT | 8945 |
rs373346374 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101521281 | TTGTCTCAAAAAAAA[-/A]GTTGTGAGCAAGTAA | 8945 |
rs373349492 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101456348 | TCAGATGTATTAAAA[C/T]AGATGATTCAAAGAA | 8945 |
rs373359440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465493 | AAACTCTTAACACAG[C/G]GTGAAGCAAAATTTG | 8945 |
rs373372387 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366919 | ATATTAATATATATT[A/T]ATATATATTTATATA | 8945 |
rs373373487 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101418502 | GAAAAATGAATACTT[A/C]ATACTTATTTTCAAT | 8945 |
rs373392987 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547228 | TTCATGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 8945 |
rs373421892 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528996 | AATACTGAATATGCT[A/G/T]TCTGCTCAGTAATGG | 8945 |
rs373440405 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101356288 | TCAGGTGTGAGCCAC[A/C]GCGCCCAGCAGAGGG | 8945 |
rs373446384 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547328 | AAATATATGGTTTTT[C/T]TTTTTTTTTTTTTTT | 8945 |
rs373456969 | snp | C/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407055 | AAATTTTCTTGTAGC[C/G]ACATTGAAAATGTGA | 8945 |
rs373472145 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101376028 | GCTGAATTAACTGGA[A/T]TCAAAAGTGATGGCA | 8945 |
rs373530849 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101542232 | CTTATTATCCTTTTA[A/G]TGCCTGTTAGGAGCA | 8945 |
rs373538962 | in-del | -/TGTA | 0.499703 | 0.0121769 | intron-variant | BTRC | GRCh38.p7 | 10:101532784 | GTGTGTGTGTGTGTG[-/TGTA]TGTGTGCGCGTGTGC | 8945 |
rs373539674 | snp | A/C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101519952 | GTGAGCCGAGATCAC[A/C/G]CTATTGCACTCCAGT | 8945 |
rs373557817 | snp | C/G | 2.37691e-05 | 0.00344731 | intron-variant | BTRC | GRCh38.p7 | 10:101521629 | TGTTTCTTTTAACCC[C/G]CTTCTACAGACAAAA | 8945 |
rs373569974 | in-del | -/T | 0.405603 | 0.195673 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514464 | CCTTTCCCTATTTAA[-/T]TTTTTTTTTTTTTGA | 8945 |
rs373578923 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | BTRC | GRCh38.p7 | 10:101464694 | GAAGAGCATGAACTC[A/T]ATGTTCTTGGAAAGA | 8945 |
rs373584277 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502461 | GAGGGCTTCCTTTTG[C/T]TCTTTTCTGTCTTCA | 8945 |
rs373608619 | snp | C/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514534 | CTAGGCTCACTATAA[C/G]CTCCACCTCCCAGGT | 8945 |
rs373611658 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505130 | ATATATATATATGTG[C/T]ATATATATGTATATA | 8945 |
rs373655647 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505104 | GCACCACTGCACCTG[A/T]GTATATATTTATATA | 8945 |
rs373657993 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531424 | AGCAAGCCCATTAAG[C/G]TTTATTGACATGAGT | 8945 |
rs373658441 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507230 | TGGAGTCTTTTAAAT[A/G]TAAGTAACACGCAAC | 8945 |
rs373660592 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356587 | CATAGGGAGAAGCCA[A/G]TTTTTTCTTTTAATT | 8945 |
rs373682757 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101382113 | TCAGCTTCCTGAGTA[A/G]CTGTTATTACAGGCA | 8945 |
rs373706715 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470656 | TTAGAAGGGATACTT[C/T]CTTTGGTCCTACCTA | 8945 |
rs373748315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500247 | TATTACTCCTAGGCA[A/G]CAAACCTGTACACCA | 8945 |
rs373753281 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442290 | TCTCTCTCTGTCTCT[C/G]TGTGTATGTGTGTGT | 8945 |
rs373758011 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400006 | TAACCATACCATCAC[A/G]AAAGAAGGCCTCACA | 8945 |
rs373809510 | snp | C/T | 0.000259968 | 0.0113981 | intron-variant | BTRC | GRCh38.p7 | 10:101526229 | TTTCTTACTCTTATA[C/T]GGCTTCAGGACCTGG | 8945 |
rs373817496 | snp | G/T | 1.64819e-05 | 0.00287066 | intron-variant | BTRC | GRCh38.p7 | 10:101538395 | CTTGCTGTTTAGAGA[G/T]CATTGGAGAGCAGGT | 8945 |
rs373827413 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101376273 | GAGGTTTCAGTGAGC[C/G]AAGATTATGCCACTG | 8945 |
rs373836731 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101403290 | AGATAGCTCATGGAA[C/G]TAAAGGGAAAAAGAT | 8945 |
rs373837653 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101411660 | ATACCCTACATCACT[A/G]TGTTCATGTTATTAT | 8945 |
rs373848469 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359927 | TTTTCTAAATTTATG[C/T]TTATAGTAGATTTTC | 8945 |
rs373887507 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101442001 | TATACTTCTTTGATT[A/T]GAATGATGGAAAAAT | 8945 |
rs373898539 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366784 | TATATATATATATAT[A/T]TATATTTTTACATTT | 8945 |
rs373907834 | in-del | -/ATG | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352557 | CTATTTCTTGAGATG[-/ATG]TCTGCACACGGTTAT | 8945 |
rs373917109 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367053 | ATATAAATATATATA[-/T]ATATAAATATAAATA | 8945 |
rs373917586 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366992 | TATATATTTATATAT[A/T]TTAATATATATATTT | 8945 |
rs373924140 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101386484 | TCATTCAAGAAAGAC[C/T]TTTTTGTGATAATTT | 8945 |
rs374003189 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101437832 | TCTTTGCATATACCG[-/T]TCTGCTTACCTGAAA | 8945 |
rs374019251 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404381 | AATTTCACCGTCTGT[G/T]CCATCTTGGTATTGG | 8945 |
rs374025337 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101376437 | GAAAACAATTTACTT[C/G]TGTAGGCTGTTTGCA | 8945 |
rs374108354 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101542721 | GGACCACAGGCGTGC[A/G]CCACCACGTCCAGCT | 8945 |
rs374130248 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101432771 | ATAGGGCAGAATCTC[A/G]GAAGGATCCAATTGT | 8945 |
rs374142837 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421793 | ATGTCCCTACAAAGG[A/G]CATGAACTTATCCTT | 8945 |
rs374149155 | snp | A/C/G | 3.29947e-05 | 0.00406159 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526073 | ATGCCAAATCACTAT[A/C/G]TGCTGCTGAACTTGT | 8945 |
rs374182940 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101476884 | ATAGCAATGGTTCTC[A/G]AAGAGTGTTCCTGGA | 8945 |
rs374196631 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396756 | GGTTTGTTGATGTTT[G/T]TTTTTACATGATGAA | 8945 |
rs374221688 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421980 | ATAATCCTCTGGGTA[C/T]ATACCCAGTAATGGG | 8945 |
rs374226066 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367059 | ATATATATATATATA[A/T]ATATAAATATATATA | 8945 |
rs374251404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363620 | TGCACCACCACGCCC[A/G]GCTAAGTTTTGTATT | 8945 |
rs374256139 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101376061 | CCAGTTGCAGTGGCT[C/T]ACGCCTGTAATCCTA | 8945 |
rs374292366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494920 | TCATCATAATTTTCA[A/G]TGTTTTAAAGTGTCA | 8945 |
rs374328135 | snp | G/T | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354569 | CTCTGGAGAAACGCC[G/T]TGAGGCCGCTGGCGG | 8945 |
rs374336611 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422351 | AATTTGTTTGAGTTC[A/T]TTGTAGATTCTGGAT | 8945 |
rs374343313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101519335 | TCCACCCACCTCATC[C/T]TCCCAAAGTGCTGGG | 8945 |
rs374345418 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445542 | CACCCGCCTGAAACT[A/G]AGAATCAACTCTTCA | 8945 |
rs374346851 | snp | C/T | 0.000120547 | 0.00776267 | intron-variant | BTRC | GRCh38.p7 | 10:101521602 | CCCTCATTTTCAATA[C/T]TAATCATTTTATGTT | 8945 |
rs374368901 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360938 | AGCCTCCTGAGTAGC[C/T]GGGACTACAGGTTTG | 8945 |
rs374391640 | snp | A/G | 9.88712e-05 | 0.00703035 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533056 | CATAACAGGATCATC[A/G]GATTCCACGGTCAGG | 8945 |
rs374423939 | snp | A/G/T | 0.00055027 | 0.0165796 | intron-variant | BTRC | GRCh38.p7 | 10:101414682 | CCATAAGCTATGAAG[A/G/T]TAGAAGACAGTGATA | 8945 |
rs374425030 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441457 | TCTAGTCACATACGT[C/G]TCATAATGTAGAAAT | 8945 |
rs374461827 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101462468 | GCGAATACCTGAAGT[C/T]GGGAGTTCGAGACCA | 8945 |
rs374474560 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356897 | GGACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 8945 |
rs374482531 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385349 | TCCAGCCTAGGTGAC[A/G]GAACGAGACTCTGTC | 8945 |
rs374540593 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421459 | TTATTTAACCTCCCT[G/T]GGTCTGTTTATTTTT | 8945 |
rs374559397 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449682 | TGGTTTACATGATAC[A/G]TATTCTTGGCTTTTT | 8945 |
rs374570010 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | BTRC | GRCh38.p7 | 10:101430492 | ATTTGCGGGCATTAG[C/T]GTATGTGTCTAATTC | 8945 |
rs374640756 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101482218 | TAGAGACAGGGTTTC[G/T]CCATGTTGGCCAGGC | 8945 |
rs374659154 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | BTRC | GRCh38.p7 | 10:101461969 | TGAATTAAAGCTTAC[G/T]TTCTTTCACAGAATT | 8945 |
rs374668043 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101455638 | AGCCTGTTACATGTT[A/G]AGGGACTAGAATTAA | 8945 |
rs374687651 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362414 | ATTTTTTTTTTTTTG[A/G]GATGGAGTTTCGCTC | 8945 |
rs374688444 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520680 | ACCAAGTTGTTGGCC[A/G]GGCACGGTGGCTCAT | 8945 |
rs374694123 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363493 | AGATGGAGTCTTACT[C/G]TGTCACCCAGGCTGG | 8945 |
rs374734958 | in-del | -/TATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101505136 | ATATATGTGTATATA[-/TATG]TATATATATATGTAT | 8945 |
rs374738468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463084 | ACAGTCTTGCTCTAT[C/T]GCCCAGGCTGGAGTG | 8945 |
rs374741700 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101457731 | GCAGTAGAATATAAC[A/G]TTAATTACATTTGAT | 8945 |
rs374754175 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428116 | ACATAATTCTAAGGA[A/G]ATATTGATGTAAATG | 8945 |
rs374757858 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101443071 | GTATTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 8945 |
rs374770908 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101393974 | TTCGTAGACTGTAGA[G/T]CATGTCCCTCTAAAA | 8945 |
rs374771148 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471188 | ATAGTTCACATTTCT[A/G]TATAAATTTTAGAAT | 8945 |
rs374786866 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516528 | ATACTCGTTTTGAGG[G/T]GTGGTGACTAAAATG | 8945 |
rs374842990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101419120 | GGTTCTGGCAATTCT[C/T]CTGCCTCAGCCTCTG | 8945 |
rs374846527 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363482 | TCTTTTTTTTGAGAT[A/G]GAGTCTTACTCTGTC | 8945 |
rs374859216 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423147 | TTGAACTCCTGGTCT[C/T]AAGCAGTCCTCCCAC | 8945 |
rs374889092 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502041 | AAATGGTGCCCATGT[A/G]GGGGACATATAAATA | 8945 |
rs374903310 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101524337 | CCAGTCACTGAGACA[C/T]GTTACTATCTCAAGC | 8945 |
rs374918864 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101522400 | AAAAAACTCTAGAAA[A/T]AAAGACTCCTTTTTT | 8945 |
rs374930785 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101491193 | GGCTCCATATTACAT[A/T]GTTCTGTATATAAAA | 8945 |
rs374937153 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101379737 | AAGTCTGAACGTTTT[-/A]TTTCCAGGAATCCAT | 8945 |
rs374942107 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517206 | AAACATCCACCTCAA[C/T]ACACCAGGATTACAG | 8945 |
rs374953066 | in-del | -/CTC | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101400056 | AGCCAATAACCTATT[-/CTC]CTGCTAAATTCCATA | 8945 |
rs374954070 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | BTRC | GRCh38.p7 | 10:101392716 | CATAGTAGAGACAGG[G/T]TTTCACCATGTTGGC | 8945 |
rs374960061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101456394 | AAAATTAGCTAGATA[C/T]GTTCAAAGAAAAAAA | 8945 |
rs374966585 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409468 | TCACTTGATGGGGAT[A/G/T]CATTCTGAGAAATGT | 8945 |
rs374966769 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355208 | GAGTTGCAAAGACCC[A/G]TAAGAAGTGATGAGA | 8945 |
rs374981630 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101527555 | CCCAGGAGTTTGATA[A/C]CAGGCTGGGCAACAT | 8945 |
rs375025952 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505839 | GATCTTTATTTAATC[A/G]AAGTGAAAACAAAAT | 8945 |
rs375027919 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488721 | AAATGAATTCAAATA[C/T]CTTCTAAAGATACAC | 8945 |
rs375045026 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418403 | ACATTTATATTTTTT[G/T]GGGGGGGTGATTTAC | 8945 |
rs375050641 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101374994 | AGAGGCCAGGTGCTG[C/T]AGGGTGGCTAGGAGT | 8945 |
rs375056894 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101505158 | ATATATATGTATATG[-/TA]TATATATATATATAT | 8945 |
rs375152152 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438917 | GTTCAATTCCAGTAG[A/T]CCTGGAAATGTGCCT | 8945 |
rs375160298 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355629 | GACTTGTCACTCCAA[A/G]TCTTACTCCTTTGCT | 8945 |
rs375176118 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555821 | AAATTTACTTTCCAA[C/T]GTAGGGCCTAAAGGA | 8945 |
rs375187441 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481141 | TAGAGATGAGGTGTC[A/G]CTGTATTGCCTAGGC | 8945 |
rs375193086 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392073 | CAACTTCTGCCTCCC[A/G]GGTTCAAGTGTTTCT | 8945 |
rs375223811 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101374671 | TAGCATTGGGAGATA[C/T]ACCTAATGCTAGATG | 8945 |
rs375229486 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507405 | AGCAGCCATCGATCA[A/G]GTTCACAAGTTAACA | 8945 |
rs375230167 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515477 | CCTCAGCAATGTTTT[A/T]TAGTTTTCAATTTAT | 8945 |
rs375230651 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101382767 | AGTTGTAAAATCAAC[C/T]TATTTATTTTTAGGT | 8945 |
rs375248040 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101549175 | CACAGTGGCCCACAC[C/T]TATAATCTCAGAGCT | 8945 |
rs375292185 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101419475 | AGCTTATTGTTGTTG[G/T]TGGTGGTGGAATTCT | 8945 |
rs375299562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374871 | CAGCTGTACTCAAAT[G/T]GTTATGTGAGAGAAA | 8945 |
rs375303578 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101397919 | CTTTCTCTGTAATCA[A/G]AGCTTCTTAAGTGTT | 8945 |
rs375312132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101522711 | CAGGTGTGAGCCACC[A/G]TACCCAGCCAAGACT | 8945 |
rs375317445 | snp | C/T | 1.64855e-05 | 0.00287097 | stop-gained, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550720 | TCCGGAAGAGTTTTT[C/T]GACTACAGTTTGATG | 8945 |
rs375325999 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101370546 | TAGTCAAGATTTTCA[A/G]TTTTTAAATTTATGG | 8945 |
rs375330472 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101541332 | TGGCGCGATCTCAGC[G/T]CACTGCAAGCTCTGC | 8945 |
rs375341693 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101518073 | GCCCGCCACTACGCC[C/T]GGCTAATTTTTTGTA | 8945 |
rs375345905 | in-del | -/TTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101359605 | CTAATTTTGTTGTAT[-/TTTTT]TTTTTTTTTTTTGAG | 8945 |
rs375357057 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505159 | TATATATGTATATGT[A/G]TATATATATATATAT | 8945 |
rs375379422 | snp | A/G | 4.94882e-05 | 0.0049741 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430404 | GGACAGCATGCCTTC[A/G]CTGCGATGCCTGTAT | 8945 |
rs375388968 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371868 | GCCAGACAGGTAATG[G/T]GCCTATGTAACAAGG | 8945 |
rs375405784 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101444595 | TCAGGGGAACAGCCA[A/G]TGTATTTATGATGAT | 8945 |
rs375409945 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498543 | CATAAGCTAATGGTG[A/G]CCACACAGGTTAGCA | 8945 |
rs375424347 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472071 | TTCCCTTTAGTGCAG[A/T]ATGGTATTTAAAAAC | 8945 |
rs375427717 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101492613 | TTTTGTAGTATTAAT[A/G]TAGTGTCATTTTGGA | 8945 |
rs375433819 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519302 | CCAGGCTGTTGTCAA[A/T]CTCCTGACCTTAGGT | 8945 |
rs375486640 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415526 | GTTATGTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs375517469 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101376281 | GTGAGCCAAGATTAT[-/G]GCCACTGCACTCCAG | 8945 |
rs375565326 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101478665 | GGCGTGGTAGCGTGC[C/T]CCTGTAGTCCCCCAC | 8945 |
rs375593157 | snp | C/T | 1.67646e-05 | 0.00289517 | intron-variant | BTRC | GRCh38.p7 | 10:101531223 | TTCACTGGGAAATAT[C/T]TGTTATTTTTTAGGG | 8945 |
rs375602017 | snp | A/C | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352260 | AAATTCAAGAACAAA[A/C]CTTTTTATTAACTGA | 8945 |
rs375605063 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377467 | TTGCTATTTTCCAGA[A/G]TGATTGTACCAGTTG | 8945 |
rs375616462 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101376608 | CTGGTAGTTTTTCCT[A/G]GTACTATGAACAGAT | 8945 |
rs375624831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425158 | TGGCTACTTAGTATT[A/C]CATGGTATATGTGTA | 8945 |
rs375665354 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101464091 | TAAATTGGGAAGTAG[A/G]AACACTCTGCCCACT | 8945 |
rs375671227 | snp | C/G | 8.28205e-05 | 0.00643455 | intron-variant | BTRC | GRCh38.p7 | 10:101532909 | AAGTCTCCACAGCAC[C/G]CCATCATCACATTGA | 8945 |
rs375683356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101386974 | TGGAAAAAAGTGAAA[C/T]GGAATCCCTTCGTCA | 8945 |
rs375693855 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101503193 | TAAACTCCTTCAGAA[A/T]GACATTTAAGCTTGC | 8945 |
rs375700557 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527793 | TCTCTCTCTCTCTCA[C/T]ATACACACACACACA | 8945 |
rs375702622 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503511 | AAGCTTTTCCTGGAT[A/G]AATTAAGAAAACAAT | 8945 |
rs375712643 | in-del | -/TTTTTTTGA | | | intron-variant | BTRC | GRCh38.p7 | 10:101473296 | CAGTAAATTTTTTGA[-/TTTTTTTGA]GATAGGGTCTCACTC | 8945 |
rs375744078 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435740 | GTTGGGTCATAGAGT[A/G]AGTGTATTTTTAACT | 8945 |
rs375746157 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363515 | CCAGGCTGGAGTGCA[A/G]TAGCGCAATCTCAGC | 8945 |
rs375761445 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400280 | ATGTAATATGGTTGC[A/G]TTTATTTATGTAGGC | 8945 |
rs375795668 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101469069 | ATGTGCTTTATATGC[A/G]ATATAAAAACGTATT | 8945 |
rs375826901 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536620 | GTTGTATTCGATTTG[A/G]TAACAAGAGGATAGT | 8945 |
rs375856564 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101387713 | TTTTTTTCTTGAGAC[A/G]GAGTCTTGCTCTGTC | 8945 |
rs375857479 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441988 | GCCTAAGATTGCATA[C/T]ACTTCTTTGATTTGA | 8945 |
rs375868661 | snp | A/G | 6.62811e-05 | 0.0057564 | intron-variant | BTRC | GRCh38.p7 | 10:101536691 | AAAAAGAGAAAATCT[A/G]CGTCTTAATCCTTCC | 8945 |
rs375889037 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353965 | AGCCTCAGTTTTTTT[-/T]CCTGGGGGAAGTTCC | 8945 |
rs375890859 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | BTRC | GRCh38.p7 | 10:101472272 | TTCTTTTCTTTTCTT[C/T]TCCTCTCTTCTCTTC | 8945 |
rs375896650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521362 | TTTGGCTTGCTAGTA[A/G]TAACATGCTTTCAGC | 8945 |
rs375901884 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428361 | TATTGATGAGAGTGA[C/T]ATGATAACAAAGTGA | 8945 |
rs375922670 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369512 | AAAGATACTCCAGGC[C/T]CTTCTTATACTTTTT | 8945 |
rs375928098 | snp | C/T | 8.26945e-05 | 0.00642965 | intron-variant | BTRC | GRCh38.p7 | 10:101536520 | ATACGTGAAAATTCA[C/T]CTGACTTAATTTTCT | 8945 |
rs375965842 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538412 | ATTGGAGAGCAGGTG[A/G]GGGAAGAAATTAAAC | 8945 |
rs375975603 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101395430 | TGCTTTATTTTCATT[A/T]TTATTGTCTAGGAGT | 8945 |
rs375976530 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101382540 | TTTTTTTCTTAGTGC[A/T]CTACTACATCAGAAG | 8945 |
rs375980263 | in-del | -/TATATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101366767 | TGGACTTAATCTAGT[-/TATATA]TATATATATATATAT | 8945 |
rs376030145 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484248 | CTCCAGATTTTGATA[G/T]AAGACTTGTTTTATT | 8945 |
rs376056546 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453055 | TTTGAGTGATTTTGT[C/T]CATGTAGCTAAAATA | 8945 |
rs376063016 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557134 | GCTTTCAGCTGGTTC[A/G]CCTCTTTGTTCTCTA | 8945 |
rs376069351 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519951 | AGTGAGCCGAGATCA[C/T]GCTATTGCACTCCAG | 8945 |
rs376072644 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473862 | CTCGGCTTCCCAAAG[G/T]GCTGGGATTACAGGC | 8945 |
rs376074298 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460551 | AATATCAAGTTAAAC[C/T]TCATAAGATATTTCT | 8945 |
rs376096083 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | BTRC | GRCh38.p7 | 10:101538415 | GGAGAGCAGGTGGGG[A/G]AAGAAATTAAACGTT | 8945 |
rs376097667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369323 | CTCCTGGGCTCAAAC[A/G]TCCTCCCACCTGGGC | 8945 |
rs376103768 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385840 | GCTTGTTTTTTTTTT[G/T]ATTCTTGCATAGTAT | 8945 |
rs376106161 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389771 | CTGAGACCACAGGTG[C/T]ACGCCACCATGCCTG | 8945 |
rs376110145 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101367007 | ATTAATATATATATT[-/TA]TATATATATTTATAT | 8945 |
rs376116691 | in-del | -/ACA | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405810 | TTATGCTAGTCAACA[-/ACA]TACACTGCAAGTTCA | 8945 |
rs376118354 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521051 | GGCAGGAAAATTGCT[G/T]GAAGCCAGGAGTTTG | 8945 |
rs376139705 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393862 | GAATTGAGTTCTTTG[C/T]CTTTTCTCATTTTCT | 8945 |
rs376173286 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422051 | GGAATTGCCACACTG[A/T]CTTCCACAATGGTTG | 8945 |
rs376186215 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101544276 | TTACCTTTTCTATTG[C/T]CTCCCATTCCTTTGT | 8945 |
rs376189574 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101403323 | CCAGTAAGGCCCCAT[A/G]AGGACTTGGAACCAG | 8945 |
rs376191226 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101363527 | GCAGTAGCGCAATCT[A/C]AGCTCACTGCCACCT | 8945 |
rs376198594 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442292 | TCTCTCTGTCTCTGT[C/G]TGTATGTGTGTGTGT | 8945 |
rs376279399 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545226 | CATTAGTTTTCAGCA[A/G]TTTGCTTATGATGTG | 8945 |
rs376316565 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534819 | CTGACATTACCCTCC[A/G]GAGGGTGCTGGTCGG | 8945 |
rs376339990 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101552357 | CAGCTAATTGTTTGT[A/T]TTTTTTTTTTTTTTT | 8945 |
rs376346441 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353910 | TTGTGGGCAACCGCA[A/G]CGCTGCCGCAGTGAA | 8945 |
rs376368261 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515528 | CCATTTTTTTTTTTT[G/T]TGAGATGGAGTCTAG | 8945 |
rs376377684 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101356199 | TAGAGTCGGGGTTTC[A/C]CTATGTTGGCCAGGA | 8945 |
rs376399669 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523363 | TTTGGAGGATGCTGT[A/G]GTTTTTCTGAATGCT | 8945 |
rs376406283 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101531604 | CACACACCTGTAATT[C/T]CAGCTACTCAGGAGG | 8945 |
rs376428739 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424113 | GTGGTGCATGCCGGC[A/T]GTCCCAGCTACTCAG | 8945 |
rs376461584 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101486404 | TGCAGTCTTTTAGTG[C/T]AGGAATTTTAAGGAG | 8945 |
rs376475109 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101499817 | ACCTTCCATTGAAAC[G/T]TAATTCTTTCAAATG | 8945 |
rs376476120 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541432 | CCCGGCTGATTTTTT[-/T]GTATTTTTTAGTAGA | 8945 |
rs376480082 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101534229 | TTTATGATAAAACCT[A/G]AGATCCAGGGTAATC | 8945 |
rs376528782 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543098 | GGGCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 8945 |
rs376577588 | snp | C/G | 0.000589667 | 0.0171606 | intron-variant | BTRC | GRCh38.p7 | 10:101479341 | TCAATATTTTAAAAA[C/G]CTGTTTCCAACAAAT | 8945 |
rs376596031 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101467327 | GATATCAGGCAGGCA[A/G]GGTTTTTTTTTTTTT | 8945 |
rs376641778 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101462620 | AGAGGCAGAGGTTGC[A/G]GTGAGCTGAGATTGC | 8945 |
rs376686163 | in-del | -/TATAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101532132 | AAAGGAAGAATATTT[-/TATAAA]TATAGATAGTAGCCT | 8945 |
rs376719289 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505128 | TTATATATATATATG[C/T]GTATATATATGTATA | 8945 |
rs376740765 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101409554 | TAGGTAGTATAGCCT[A/G]CTATATACCTGGGCT | 8945 |
rs376742991 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404999 | CTAGAATCCATCTTA[A/T]AAAAAAAAAAAAAAA | 8945 |
rs376752452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420965 | AATCGCTACAGGTTT[A/G]TACTCATATTTTCAT | 8945 |
rs376775994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429583 | TCTCCTTTCTCTCTC[C/T]TTTCTCTCTCCTTTT | 8945 |
rs376790651 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415501 | TTTATGTTATGTTAT[G/T]TTATGTTATGTTATG | 8945 |
rs376827632 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411928 | CTCTTGTGGCTGATT[G/T]TAAGCTTTATTCTGA | 8945 |
rs376832375 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407208 | ACCAAAAAAATTAGG[C/T]GTAGTGGTATACACC | 8945 |
rs376842045 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537126 | TCATCCTAGCATTTC[A/G]TTTATGAGTTTAGTC | 8945 |
rs376870422 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495094 | TTCTATTTTCCTCTA[C/T]CAAAGAGCAGGGTTC | 8945 |
rs376880904 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101508937 | AAAAAAAAAAAAAAA[A/C]TAAAAGTAGAATGTT | 8945 |
rs376892986 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367004 | TATATTAATATATAT[A/T]TTTATATATATATTT | 8945 |
rs376895237 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421428 | GTTGCTTACTAACTA[C/T]TCATCAACGTGTAAT | 8945 |
rs376916564 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101471941 | TTGGGCTACTGAAAG[A/C]CTCTTTCGGCAGGCT | 8945 |
rs376917099 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385385 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAAAGTG | 8945 |
rs376924664 | snp | A/G/T | 0.00010075 | 0.00709696 | intron-variant | BTRC | GRCh38.p7 | 10:101550648 | CTGAATTTGTGTCCT[A/G/T]TTGATTTTGAGTAGT | 8945 |
rs376975761 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538300 | ATCTTTAGAAAAATT[A/G]AAGTGTGGGATCTTG | 8945 |
rs376991704 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101413300 | AGGTGCCCACCACCA[A/C]GCCTGGCTAATTTTT | 8945 |
rs377018854 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101501124 | CCTGAACCTGCGGGG[C/T]AGAGGTTGCAGTGAG | 8945 |
rs377020650 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366786 | TATATATATATATAT[A/T]TATTTTTACATTTAT | 8945 |
rs377052940 | snp | C/T | 3.46981e-05 | 0.00416508 | intron-variant | BTRC | GRCh38.p7 | 10:101532451 | AGGTCTATTCAGTTG[C/T]AGAAAGGTAGCAGAG | 8945 |
rs377089418 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547237 | GAACCCGGGAGGCGG[A/T]GGTTGCAGTGAGCCA | 8945 |
rs377120605 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406472 | CCCGGCCTACTGCTT[A/G]TACTCTTTGTTCCGA | 8945 |
rs377123253 | snp | A/G | 6.86507e-05 | 0.00585838 | intron-variant | BTRC | GRCh38.p7 | 10:101526005 | TTGCCTCCTCCCCCT[A/G]CTGAAAGCTCGGGGA | 8945 |
rs377191200 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556507 | CAGTCCAACCCAGAT[C/G/T]AGTGCAGCCCGGAGG | 8945 |
rs377201447 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101480620 | TTTGGAGAACACAAA[C/T]GTTCAGACCATAGCA | 8945 |
rs377208510 | in-del | -/GTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101389117 | TGTGATTTTTTGTGT[-/GTG]TTTTTTTTTTTTTTT | 8945 |
rs377211993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101388705 | CATGTTGCCTAGGCT[A/G]GTCTTGAACTCCTGG | 8945 |
rs377216380 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101548667 | TGAGGCAGGAGAATC[A/C/G]CTTGAACCTGGGAGG | 8945 |
rs377228964 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511711 | ATTTTTAATAGAGAC[A/T]GGATTTCGCTATGTA | 8945 |
rs377238091 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101522297 | CACCTGCCTCGGCCT[A/C]CCAAAGTGCTGGGAT | 8945 |
rs377240232 | snp | C/G | 2.32566e-05 | 0.00340995 | intron-variant | BTRC | GRCh38.p7 | 10:101521630 | GTTTCTTTTAACCCC[C/G]TTCTACAGACAAAAC | 8945 |
rs377244899 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421802 | CAAAGGGCATGAACT[C/T]ATCCTTTTTTATGGC | 8945 |
rs377279265 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436882 | AGTGAAATGTTAAAA[C/T]GGAACAATACAGGAA | 8945 |
rs377310634 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539202 | TTTGGGGAAAAAAGT[A/G]ATTCAAAAGGAGGAA | 8945 |
rs377313533 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393795 | TGGCATGTGCACACC[C/T]TGCTTTGGAAACCAC | 8945 |
rs377316742 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427036 | CCTTCCGAATGACTG[A/T]GAGATTTTTTTCTAC | 8945 |
rs377323918 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456371 | TCAAAGAAAAAGTTT[A/G]TAGACTGAAAATTAG | 8945 |
rs377328025 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101522367 | TAAAAAAAAAAAAAA[-/C]AAAAAAAAACAAAAA | 8945 |
rs377332137 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492246 | ATACAGTTTTGGGTT[G/T]GTTTGTTTGTTTTCA | 8945 |
rs377358967 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398333 | TGTTTTTTTGAGACG[A/G]ACTCTTGCTCTGTCG | 8945 |
rs377370155 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517597 | TGCCTTAAGTAAATA[C/T]GCCAAAGATCCATCA | 8945 |
rs377394888 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366967 | ATATATATTTATATA[A/T]ATATATATTTATATA | 8945 |
rs377410478 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440087 | AGCTCATTAGGTAAT[A/G]TGGAAGAAACATTAT | 8945 |
rs377413497 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101419099 | CACTGCAACCTCTGC[C/G]TCCCAGGTTCTGGCA | 8945 |
rs377416656 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410757 | GTCAACTGTTCTTAG[A/G]GATATGATTTACAAA | 8945 |
rs377451044 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534708 | ACACGTTGATTCACC[A/G]TTGTGAAGCAGTTCT | 8945 |
rs377495074 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101489052 | ACAAAAGTACCTCAC[A/T]TCCCCCTAGTACCAT | 8945 |
rs377542603 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101484739 | AGGCTGATGTGGTTG[A/G]AAAAACTGTGGAGTA | 8945 |
rs377549407 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101476542 | AATGGCATAATCATA[A/G]CTCCCTGCAGTCTTC | 8945 |
rs377551438 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436672 | GATAGATAGATAGAT[A/T]TATATGGCCCTAGAA | 8945 |
rs377555845 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418503 | AAAAATGAATACTTA[A/T]TACTTATTTTCAATA | 8945 |
rs377563531 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549991 | CTACCGATGGTTTTA[C/G]AAAGTAGCAAAGTTT | 8945 |
rs377580727 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101359013 | CCAAGTTTGTGGGTC[A/C]TAATGCTAGGAATGT | 8945 |
rs377580878 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101498728 | AGCCGTGGTGGTTCA[C/T]GCCTGTATTCCCAGC | 8945 |
rs377614406 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101405053 | GGGTTATATCCACCC[A/G]TGTGCAGCTTGGGGG | 8945 |
rs377616390 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438459 | AAAAAAAGTCTTCTC[A/G]TTAGCAATATAAGTA | 8945 |
rs377632358 | in-del | -/GGTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101543682 | ATATCTCACTAATTT[-/GGTG]AGGAGGGACCTAGGG | 8945 |
rs377635599 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366643 | GAAGTAACTTGGGTA[A/G]AGGCCAGGAGATCAG | 8945 |
rs377663949 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399114 | TGCGCCACCATCCCC[A/G]GCTAATTTTTTTGTA | 8945 |
rs377664597 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101358007 | CTAAGAAGAGAAATG[A/C]AAATGATTGAGGGAA | 8945 |
rs377666846 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441740 | CAAAAAATTAGCCAG[G/T]CGTGGTAGTACATGC | 8945 |
rs377683037 | in-del | -/A | 0.422944 | 0.180528 | intron-variant | BTRC | GRCh38.p7 | 10:101522378 | AAAACAAAAAAAAAC[-/A]AAAAAAAAAAAACTC | 8945 |
rs377686698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101550310 | TTTTTTTTTAGACAG[A/G]GTCTCACTCTGTTGC | 8945 |
rs377738704 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389117 | TGTGATTTTTTGTGT[-/G]TGTTTTTTTTTTTTT | 8945 |
rs377764406 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421203 | CTTTTGATGTACGTT[A/C/G]TCTTCTCCATGGCCA | 8945 |
rs386372266 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362406 | GCAAGAAATTTTTTT[-/T]TTTTTTGAGATGGAG | 8945 |
rs386372268 | in-del | -/TTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101411715 | AATTTCATTGTCAGT[-/TTTT]TTTTTTCTGGGTCTG | 8945 |
rs386372269 | in-del | -/CA | | | intron-variant | BTRC | GRCh38.p7 | 10:101486432 | AGAAAAGCGTGGCAC[-/CA]ATTTCTCAGGGAAAA | 8945 |
rs386372271 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101541276 | TCTCTTTTTTTTTTT[-/TT]TGAGACGGAGTCTCG | 8945 |
rs386747072 | multinucleotide-polymorphism | AA/GC | | | intron-variant | BTRC | GRCh38.p7 | 10:101358890 | TTGATAGGAAGGGTG[AA/GC]GTGCATAAACAAGGA | 8945 |
rs386747073 | multinucleotide-polymorphism | GT/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101363467 | TTTGTTTTTGTTTTT[GT/TC]TTTTTTTTGAGATGG | 8945 |
rs386747074 | in-del | GG/TATGA | | | intron-variant | BTRC | GRCh38.p7 | 10:101364137 | TGGTAAGATGCTTAT[GG/TATGA]CAACTATTGTGCTTT | 8945 |
rs386747075 | in-del | CTA/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101373365 | GAGACTGGGCTTGAG[CTA/T]GGGCAGTAGGTATGG | 8945 |
rs386747076 | multinucleotide-polymorphism | AA/GC | | | intron-variant | BTRC | GRCh38.p7 | 10:101409075 | CAAAAAACAAAAAAA[AA/GC]CACACAAAACATTGA | 8945 |
rs386747077 | multinucleotide-polymorphism | AA/GC | | | intron-variant | BTRC | GRCh38.p7 | 10:101421820 | CCTTTTTTATGGCTG[AA/GC]TACTATTCCATGGTG | 8945 |
rs386747078 | multinucleotide-polymorphism | CA/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101538818 | TTTGGGAGGTCAAGG[CA/TG]GATGGATCACCTGAG | 8945 |
rs397686542 | in-del | -/T | 0.375 | 0.216506 | intron-variant | BTRC | GRCh38.p7 | 10:101528301 | CTTTTACCTTTGGCA[-/T]TTTCACATCCATCTG | 8945 |
rs397689116 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101417019 | AAATTGTTTTTTTTT[-/T]CATAAACCACTTGAG | 8945 |
rs397704786 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101450009 | TGTAAAAAAAAAAAA[-/A]CTACTTGAAAGGGTA | 8945 |
rs397714575 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101490113 | CCCCCATTTTTTTTT[-/T]CAGGGTGTGTTTCCA | 8945 |
rs397726070 | in-del | -/TTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101411721 | ATTGTCAGTTTTTTT[-/TTTT]CTGGGTCTGCTTCCA | 8945 |
rs397727835 | in-del | -/C | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101546299 | TACAGTGGTATTCAC[-/C]TAATGGAAAGATAGC | 8945 |
rs397730230 | in-del | -/AATAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101381135 | TGGTGATAATAATAA[-/AATAA]CAATAATAATGGCAG | 8945 |
rs397734699 | in-del | -/CA | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101486433 | GAAAAGCGTGGCACA[-/CA]TTTCTCAGGGAAAAA | 8945 |
rs397764425 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358270 | GGCTATTTTTTTTTT[-/T]CTTTTTTGTTTTTGT | 8945 |
rs397775820 | in-del | -/AT | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101420074 | AATAATATATTCATG[-/AT]ATATATATATATATG | 8945 |
rs397782514 | in-del | -/A | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101429880 | TAAAAAAAAAAAAAA[-/A]CTCTCTTAACTGTGG | 8945 |
rs397783445 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417018 | CAAATTGTTTTTTTT[-/T]TCATAAACCACTTGA | 8945 |
rs397794235 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407741 | TCTTTTTTTTTTTTT[-/T]GTGAGACAGTCTCGT | 8945 |
rs397805526 | in-del | -/GA | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101527361 | ACCAAATGCCTCAGA[-/GA]TTTTTATCATTCTGG | 8945 |
rs397813559 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101364506 | AGTTTTAACAGCTTT[-/T]CCATCTCTTCGCTGC | 8945 |
rs397821657 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415196 | TTTGTCTTTTTTTTT[-/T]GAGACAAGGTCTTCT | 8945 |
rs397827041 | in-del | -/T | 0.375 | 0.216506 | intron-variant | BTRC | GRCh38.p7 | 10:101447891 | GTTTATCACTTTTTT[-/T]CTTTAATCAACCAAG | 8945 |
rs397828907 | in-del | -/A | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101410708 | ACAACTCAAAAAAAT[-/A]AAAAAAAGACAACTC | 8945 |
rs397844462 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389613 | TTTGCCAAACACCTT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs397844788 | in-del | -/A | 0.392353 | 0.205513 | intron-variant | BTRC | GRCh38.p7 | 10:101467196 | CCTTTTCTTCCTTTA[-/A]AAAAAAAAAAAAACA | 8945 |
rs397845322 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389612 | TTTTGCCAAACACCT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs397846904 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101522353 | CTGGTATAAAGCTTT[-/A]AAAAAAAAAAAAACA | 8945 |
rs397958280 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101501200 | TCAAAAAAAAAAAAA[-/A]GAGGTGTATGCTTAA | 8945 |
rs397969121 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101456547 | ATTTTGAGACAGTTT[-/T]AAGCTTATCACCTGA | 8945 |
rs397974709 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543625 | TGCTCTTTTTTTTTT[-/T]CTTTTTTATCTCAGT | 8945 |
rs398014626 | in-del | -/TT | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101405017 | CAGTAAGGCATAGAC[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs398040309 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101510529 | ACATCTAACAACGAC[-/T]TTTTTTTTTTGTTTT | 8945 |
rs398046207 | in-del | -/A/T | 0.00247729 | 0.0351071 | intron-variant | BTRC | GRCh38.p7 | 10:101360058 | AGATCTCTTTTTTTT[-/A/T]AAAAAAACTTAATTG | 8945 |
rs398046208 | in-del | -/T | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101411786 | TTGTGCCTCTTGTCT[-/T]GTAATTTTAGATTTA | 8945 |
rs398046209 | in-del | -/CCT | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101479215 | TATCTTTGCCCTCCT[-/CCT]TTTCTAACTTACCTC | 8945 |
rs398046211 | in-del | -/TT | 0.5 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101552373 | TTTTTTTTTTTTTTT[-/TT]GGAGAGATGGAGTTT | 8945 |
rs398046342 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352735 | AACGAGACTCTGTCT[-/A]AAAAAAAAAAAAAAA | 8945 |
rs398054657 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101429879 | TCTAAAAAAAAAAAA[-/AA]CTCTCTTAACTGTGG | 8945 |
rs398075467 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101415041 | ATCTTAACCATTATA[-/A]AGTCTATAGTAGTGT | 8945 |
rs398075468 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101456546 | GATTTTGAGACAGTT[-/T]TAAGCTTATCACCTG | 8945 |
rs398097174 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371196 | TTGGTGTTTTTTTTT[-/T]CCCCCAGAGACGGAG | 8945 |
rs398114691 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385839 | GCTTGTTTTTTTTTT[-/T]GATTCTTGCATAGTA | 8945 |
rs398114692 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418630 | ATCTGCTTTTTTTTT[-/T]GCCAAACATATATAT | 8945 |
rs398114693 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496021 | TATTTTTTTTTTTTT[-/T]ACTGTCTGAATTATT | 8945 |
rs398114694 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101510518 | CATCTTAAAAAAAAA[-/A]CAAAAAAAAAAGTCG | 8945 |
rs398114696 | in-del | -/TTTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101520159 | TTGTTTGTTTGTTTG[-/TTTG]GGGGGACAGAGTCTC | 8945 |
rs527241104 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101530795 | CTGAAATCAGGCTTA[A/C]CTTTGCTCCTCCGCA | 8945 |
rs527245647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421514 | GGTACATGTGCACAA[C/T]GTGCAGGTTTGTTAC | 8945 |
rs527248953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520976 | CAAAAACAAAAAAAA[A/G]GTTGTGATGACGGAG | 8945 |
rs527255954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470827 | TTCATTATTTTTGCC[A/G]TAATTTCATTCAGTT | 8945 |
rs527256168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461661 | TGTCATCAGCTAAGT[A/G]TGGGCTGGAACTTTC | 8945 |
rs527259189 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543464 | CCATGTTTTTTTTTG[-/T]TTTTTTTTTTTTCTT | 8945 |
rs527259702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356907 | AGGCCGAGGCAGGCG[A/G]ATCACGAGGTCAGGA | 8945 |
rs527276512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101412596 | CTTAATGTACTAGAA[A/G]TCCTCATATTACATA | 8945 |
rs527279506 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101522341 | CACCACGCCCAGCTG[A/G]TATAAAGCTTTAAAA | 8945 |
rs527292556 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486687 | TTCAGGCAGGGTTTA[A/G]CTAACATTTTTATAA | 8945 |
rs527293642 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101520246 | CCTCCTGGGTTCAAG[A/C]GATTCTCCTGCCTCA | 8945 |
rs527330134 | snp | A/C/G | 9.89114e-05 | 0.0070319 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521824 | TGGGCACATAAACTC[A/C/G]TATCTTAAACCTATG | 8945 |
rs527334858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404093 | CTGGAGTGCAGTGGC[A/G]CATCTCAGCTCACTG | 8945 |
rs527353024 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465404 | GGAGAGCTATTTAAA[C/T]ATTGGAGGAGCAAAC | 8945 |
rs527361636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514300 | TGCCTATTCCAAGAA[C/T]GTCAAGGTTTTCTCC | 8945 |
rs527384541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454641 | AGAAAAATTAGCCTG[G/T]TGTAGTGGCGTATAC | 8945 |
rs527409609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396126 | GTTCTGTTATAGCGA[A/G]TACTGGTACAACAAA | 8945 |
rs527415712 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498603 | CCTCCTGGGGAATTT[A/G]GCATTAAGTTTCTAT | 8945 |
rs527435695 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101469861 | ATGCTATATTTTTGG[G/T]GTCTGACATTCACTT | 8945 |
rs527438079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427969 | ATAAAGAAGTAATAT[A/G]AGTAGAATGTGATTC | 8945 |
rs527438218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436814 | TTCAGGAGAGATGTT[A/G]TATTTTATTCCTTAA | 8945 |
rs527455455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371259 | AATGGCACCATCTTG[A/G]CTCACTGCAGACTCC | 8945 |
rs527496494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101485961 | CTTCTCCAAAAGTCA[A/G]ACGATCAATTCGCCT | 8945 |
rs527524199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101428799 | GGGATATACATAGAT[C/T]TCCTTTGGATTTATT | 8945 |
rs527536072 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101373731 | GACCATCCTGGCTAA[C/T]ATGATGAAACTCAGT | 8945 |
rs527542771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478162 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCGCCT | 8945 |
rs527558060 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409194 | ACATTTACATCATTC[C/T]AAGTAAAAGCTTTTA | 8945 |
rs527586365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364152 | TATGACAACTATTGT[C/G]CTTTCTTCTTTCTGC | 8945 |
rs527601186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539247 | TATCATGTTGTTAGC[C/T]AAGGGCCCAGATTGA | 8945 |
rs527618911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101472684 | TCTGGGCATGGTGGC[A/G]CACACCTGTAGTCCC | 8945 |
rs527624783 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438382 | GTGAGCCGAGATCGC[A/G]CCACTACACTCCAGC | 8945 |
rs527627451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470174 | CTTTTTATTATTGAG[A/T]TGTAGACTCAACTGT | 8945 |
rs527649286 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101412430 | GATTACATTCTGGCA[C/T]TGTTTGTTGTTCAGT | 8945 |
rs527664628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549095 | ATACATACTATATGA[G/T]TATATTTATATGAAA | 8945 |
rs527746492 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | BTRC | GRCh38.p7 | 10:101472267 | CCTTTTTCTTTTCTT[C/T]TCTTTTCCTCTCTTC | 8945 |
rs527754226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101414278 | TACACGATGGTGGTC[C/T]CTTGAGATTATAATG | 8945 |
rs527767900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366254 | ATAGTGTACCTGTAA[C/T]GTAATTTGATAAAAA | 8945 |
rs527768421 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101374370 | CACAATAGCAAAGAC[C/T]TGGAACCAACCCAAA | 8945 |
rs527774083 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386040 | GAGATGACTTGGCTG[A/G]TAGTTATCAAAAATC | 8945 |
rs527788641 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101382521 | ATAATATATGCTGTG[-/T]TTTTTTTTTTCTTAG | 8945 |
rs527826745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358806 | CTAGATTTGGAAGTC[C/G]AAGAATGTCACTGTG | 8945 |
rs527835119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472706 | TGTAGTCCCAGCTAC[G/T]TGGGAGGCTGAGGCA | 8945 |
rs527843455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515060 | TCCCGGGTTCAAGCA[A/G]TGCTCCTGCCTCAGC | 8945 |
rs527844886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101505615 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAATAAA | 8945 |
rs527869320 | in-del | -/TA | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101537063 | ATTTCTTGGGTTTTT[-/TA]TCTCTTTGAGTAATT | 8945 |
rs527872610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446559 | AATTCTTGCTTTTTT[C/G]GCTACTGCTATTGTA | 8945 |
rs527877976 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101419472 | CCAAGCTTATTGTTG[G/T]TGGTGGTGGTGGAAT | 8945 |
rs527878251 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555256 | TATTGCCCAATAGCC[A/G]TAATTTTACCAGCCT | 8945 |
rs527889719 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101523206 | AGACTCCATCTCAGA[-/AAAT]AAATAAATAAATAAA | 8945 |
rs527890122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496528 | TCAGGCAGTCCTCTT[C/G]CCTCAGCCTCCCAAA | 8945 |
rs527915779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388736 | CCTCAAGCAATCTGC[C/T]CACCTCAGCCTCTCA | 8945 |
rs527917237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396690 | AGTCTGTGGAAACAT[C/T]AGTCACTACTAACGG | 8945 |
rs527940717 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555997 | TTAACTTGGTGTGCA[A/G]TTTGAAAGGATGTGA | 8945 |
rs527951760 | in-del | -/CAGT | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101393378 | ACCCCAACTTGAAGC[-/CAGT]CAGTCAGAAGCTCCA | 8945 |
rs527973659 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101380387 | CCTCTTTTTTTTTTT[A/T]AATTAAAAAGTAAAC | 8945 |
rs527974329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101497306 | GTTATTTTCATTTCC[A/G]TATAAATTTTAGAAT | 8945 |
rs527978717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389349 | TACTTTGGGTTATTA[C/T]CATTTCTTTTATGGA | 8945 |
rs527996309 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101381148 | TAACAATAATAATGG[C/T]AGCCAACACTTGTAG | 8945 |
rs528001900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548220 | CTACCCCGTGGCCCA[A/G]CAAGTCTACTCCTAG | 8945 |
rs528006559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101438305 | TGGTGGGCGCCTGTA[A/G]TCCCAGCTCCTCGGG | 8945 |
rs528018191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487993 | ATATATTAATAATCT[A/G]TAGACTGTAATTCTA | 8945 |
rs528018524 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101443626 | TAATTTCTTCTATGT[A/G]ATCTTCATTATTAAA | 8945 |
rs528022435 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505953 | GGAGTCTCGCTGTGT[C/T]GCCCAGGCTGGAGTG | 8945 |
rs528104972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544046 | TCCAGAGTAGCTGGG[A/T]CTACAGGCGCCCGCC | 8945 |
rs528107310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101508996 | AATTTCCTTTTTTCT[A/G]CATGTTCAATTTGTA | 8945 |
rs528112483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101434701 | CAGGAAGCTGAGGCG[A/G]GAGGATTGCTTAAGC | 8945 |
rs528117882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493340 | TATGATGTACTAGGC[A/C]TATACATTTTCACTG | 8945 |
rs528121877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101376649 | CTTCATTTATTTTAA[A/G]GATGCTGTGGCTGGT | 8945 |
rs528152029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427112 | CATTTCTTTTTTCTT[C/T]CTTTTTTTTTTTTTT | 8945 |
rs528166999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417709 | TTCATTTTAGAGATA[G/T]GGTCTTGTTCTTTCA | 8945 |
rs528186785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377177 | TGTTACTGACCTCTT[C/T]CGTTCAGCATAATGC | 8945 |
rs528190514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536329 | GCCCTGTGCTTTGAA[A/C]ATACATTTTACATTT | 8945 |
rs528194646 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101362193 | CTCGATCTCCTCCTT[A/G]TGATTCGCCCGCCTT | 8945 |
rs528254860 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419954 | TCTGGTTCCTTTTAG[C/T]GGAGAGTGATATTTT | 8945 |
rs528277675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449829 | GATTGCTTTTTTTTT[C/T]CCCTGAAAGAATGGT | 8945 |
rs528283242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509703 | GACTACAGGCATGCA[C/T]CACCACACACAGCTA | 8945 |
rs528288423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459123 | AATTTTAGCACCCAA[A/T]GATGATTCTTCCTTA | 8945 |
rs528305615 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101450491 | AGTATCTCAGTGCTT[A/T]GTTGAGCTTGTTTAT | 8945 |
rs528306607 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | BTRC | GRCh38.p7 | 10:101385740 | TCCCAGACACACACA[C/T]ACACATATGTTTTGT | 8945 |
rs528306761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499738 | TACTATGTAGGCCTA[C/T]GAGATTGCTCACTAT | 8945 |
rs528336529 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449411 | TACTTAAGAAAATCT[A/G]CAGAGGTCGAGTTAC | 8945 |
rs528341280 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101384011 | GCTTGTATCACCATG[A/C]CCTGTCTAGGTTATT | 8945 |
rs528351307 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101378433 | GTGAGTTTTACAGTT[-/A]ATTTAATCTTTGTTT | 8945 |
rs528369219 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101361973 | ATATTTTTTTTTCTT[A/C]CCCCTTGAGACGGAG | 8945 |
rs528379801 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359011 | GGCCAAGTTTGTGGG[C/T]CATAATGCTAGGAAT | 8945 |
rs528387487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101442432 | CGTGGTCTCCAGGGA[A/G]GAGAAAATACAGCGT | 8945 |
rs528391224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384763 | GAGAGATTATTTTTC[C/T]TATTGAGAAGTAAAA | 8945 |
rs528391756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551611 | AGAAGGCTGCCCTAG[A/C]TGCTGAGGAGCGTTG | 8945 |
rs528441160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511857 | AGTTTCACTATGTTG[A/C]CCAGGCTGGTCTCGA | 8945 |
rs528465240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452552 | GCATCTGTAGTGTTA[C/T]ATGATTAGTGTCGGA | 8945 |
rs528475866 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101545970 | GAGCATCAAAACATA[C/T]GAGGCAAAAAACCAT | 8945 |
rs528479589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101503560 | AGAAATGTCTTCAGT[C/T]CCTTGATGTTCCCAG | 8945 |
rs528506012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444837 | AGTGAACAAATTTCC[A/T]TTCTCAAGAGCATGG | 8945 |
rs528529498 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394418 | CAGCATCCTGCTTGC[A/C/G]TGGCTTGTGGATTTC | 8945 |
rs528563150 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493039 | GCCCTTGAAACTTCT[A/G]AAGTTGGAGGTTTCA | 8945 |
rs528575236 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101386963 | TGGGTTTGATGTGAC[A/G]AAGGGATTCCGTTTC | 8945 |
rs528576599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504299 | CTTGATGTTTATTGT[G/T]TGGGAGAGGATGTTT | 8945 |
rs528586916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378452 | TAATCTTTGTTTTGG[G/T]GGTGTTAGTCATGTC | 8945 |
rs528595745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387734 | TTGCTCTGTCGCCCA[A/G]GCTGAAGTGCGGTGG | 8945 |
rs528607571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101364646 | GTGGATAAATATTTT[C/T]GTAGCACAGATTCAT | 8945 |
rs528618001 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101456155 | GCCTGGGTGACAGAA[C/T]GAGACTCTGTTTCAA | 8945 |
rs528619228 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553860 | AGAGAGTGTCCTCCT[C/T]TCACATGAGCCAGAT | 8945 |
rs528636824 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101468180 | TATTTGTATTTTAAT[A/G]TAATCATTCTTTGAT | 8945 |
rs528641392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101418670 | TTTTCTCCCTGGCTG[C/T]ATTGCTGTATAATTG | 8945 |
rs528645488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362679 | GGATTACAGGTGTGA[A/G]CCACCACGCCCGGCC | 8945 |
rs528652510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527532 | CCAAGGCAAGAGGAT[C/T]GTTTGAGCCCAGGAG | 8945 |
rs528723429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460357 | CAAGCTTTGTAGTCA[C/T]TAATTCAATTATATC | 8945 |
rs528724141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391043 | GAATTTTGCCTAAAG[A/G]ACTTTTCTTGAAACT | 8945 |
rs528727193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101410810 | CACAGCCTGGAAATA[C/T]TTCACTTCACATATA | 8945 |
rs528736913 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101528465 | TAATTACCACTTTTT[C/T]CCCCTATCTCTTTAT | 8945 |
rs528759620 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397597 | TGTGAATAATGATTT[C/T]TTTGGTAGCAAATTT | 8945 |
rs528759892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355147 | TAAAATGTGGAGGCC[A/G]GGTGCTTTGTATCAT | 8945 |
rs528760343 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101460869 | TAGAACGTTATGACT[A/G]TATGTAATGTAAGGA | 8945 |
rs528818695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402870 | AGCATCCAGAGGTTA[C/T]AACAATAGTGTGAGT | 8945 |
rs528822295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355777 | TTGGAATCTAGTCAA[A/G]TTCACTAAAACTTTA | 8945 |
rs528850959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516095 | TTAATGAAAATTAAA[A/G]TAGAAAAAATATATA | 8945 |
rs528909881 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448267 | TATTGGAGAAAAAAC[A/G/T]TCTTTTAAAAATTTG | 8945 |
rs528911319 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101427504 | CTTCCTTCCTTCCTT[-/C]CTTCTCTTTCTTCTC | 8945 |
rs528914808 | snp | A/C/G | 1.64817e-05 | 0.00287064 | missense, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536546 | TTTCTCTTCCAGATT[A/C/G]TGGGACATAGAATGT | 8945 |
rs528937138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398319 | TTTTTTTCTTTTTTT[C/G]TTTTTTTGAGACGGA | 8945 |
rs528952543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498281 | GCCTCAGCCTCCCTA[A/G]TAGCTGGGACCACAG | 8945 |
rs528955450 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556857 | AGCACAGCTGGCGCT[C/G]TTAGCTCCTGATTGG | 8945 |
rs528992090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489551 | GATCGCTTACAAAGC[C/T]TGTGAAACCTGAGCC | 8945 |
rs528992149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498754 | CCAGCACTTTGGGAA[A/G]CCAAGGCAGGCAGAT | 8945 |
rs528992850 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101391101 | TATGGAATACAATCT[G/T]ATTTGTCTTTTAAAA | 8945 |
rs529027883 | in-del | -/CT | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101394183 | TATGAAAGAAGGGGA[-/CT]CTGGTAATTAATTTT | 8945 |
rs529049570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366136 | AGGAAATTTAGGACT[A/G]TATGATCCTAAATTG | 8945 |
rs529073354 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101506997 | AGGAATCCAGAATTA[C/T]TTTTTGAAGGATTTT | 8945 |
rs529076612 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555298 | GCTGCTATTACAAAG[C/T]GGAAGCTGTTGAATG | 8945 |
rs529100725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414189 | ATTTGACTACTCTAG[G/T]TAACTCATATAAGTG | 8945 |
rs529118587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101472658 | TGTCTCTACTAAAAA[C/T]ACAAAAATTATCTGG | 8945 |
rs529120064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463612 | AGCACCCACCGTGAA[A/C]ATGATGCTTATTTGA | 8945 |
rs529126283 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404319 | ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCAATCC | 8945 |
rs529139159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101415069 | TGTACAATAATGTCC[C/T]AGACCTTCACGTTTA | 8945 |
rs529146427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532496 | CACATTCATAGCGCA[A/G]TCTAAAGCATAAACT | 8945 |
rs529147855 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101390158 | ATCCCAGTGCATGAC[-/AT]GTGGTAGACAATAAA | 8945 |
rs529148599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522748 | ACCTATCTTCTTACT[C/T]ATGCCCTTCTATTCA | 8945 |
rs529156038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464323 | GAGAGAATCATGCCT[A/G]TTAAGTCCAGCACAT | 8945 |
rs529161806 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101387310 | GTATCTCAGTCATTT[-/A]TTTTTTTTTGTATTG | 8945 |
rs529164575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358768 | CAGGAGACAGGAGGT[A/G]GAGACTGCCAGTCTT | 8945 |
rs529165557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406104 | TTGTTAGTAGTGGTA[C/G]ATATACTTTTAGGAT | 8945 |
rs529177179 | in-del | -/CTCTATCGCC | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101463078 | TGAGACACAGTCTTG[-/CTCTATCGCC]CAGGCTGGAGTGCAG | 8945 |
rs529203841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524645 | ATCAGGAACAATTTG[A/G]TGGCACCCATTAAAA | 8945 |
rs529213052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359253 | TTTACATCAGTGAAA[C/T]TGATTACCAGGTAGT | 8945 |
rs529236312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425093 | CGCTTAGGATAATGG[C/T]TTCTAGCTGCATCCA | 8945 |
rs529250625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474314 | GTCAGGTGTATTTTG[A/G]TTTTGCCCTTAGTCC | 8945 |
rs529253604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360308 | GATCCGCCCACCTTG[A/G]CCTCCCAAAGTGCTG | 8945 |
rs529263316 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101542253 | GTTAGGAGCATAGTC[C/T]TGTTTCCTTTTTTGG | 8945 |
rs529274376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416286 | GAATCTGTCTACTTT[A/G]TTGTTTGCCTTTTCC | 8945 |
rs529278223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101497857 | AAACCCCATCTCTAC[A/G]AAAAACACAAAAATT | 8945 |
rs529289372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525545 | CTTAGTGCCTCTCCC[C/T]TAGTACATTTAAAGG | 8945 |
rs529297196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101407755 | TTGTGAGACAGTCTC[A/G]TTCTGTCGCCAGGCT | 8945 |
rs529347138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361291 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 8945 |
rs529369959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400162 | GTTATTTATTTCATA[C/T]ATTGTAGCTGCCAAT | 8945 |
rs529370908 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101466410 | GAGGCCAAGAAGCTA[A/T]CAAAGTAGCTGTCTC | 8945 |
rs529375870 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509444 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTTT | 8945 |
rs529406713 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483793 | ACAGTCATTATTAAC[A/C/T]GTCAACTTAGTCTTT | 8945 |
rs529407645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101458525 | GGGGAAACAATCAGG[A/G]AATTAATATTGATAC | 8945 |
rs529413517 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353774 | AGGCAAGCCGCTACT[A/G]GCGTCGCTCGGTAAC | 8945 |
rs529461517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101431432 | TGTGCGAGAAACTTA[C/T]AGAGAAATAATGTGG | 8945 |
rs529466904 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101385671 | CAAGGCTTCTTAACC[-/T]TTTTTTTGGTTATGG | 8945 |
rs529467321 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512057 | CTCTTCAGAGAAGGC[A/G]AAGACACTTTGTATG | 8945 |
rs529467478 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490500 | TCACATCTTTAAATG[A/T]TAGAGTCAAGTTTTG | 8945 |
rs529472986 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101549607 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8945 |
rs529473664 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101374729 | ATGGCACATGTATAC[A/G]TATGTATGTAACCTG | 8945 |
rs529480438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510465 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 8945 |
rs529493484 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447006 | TGGGGGGTGGTGGGG[A/G]GGCCGGTTACAAAGC | 8945 |
rs529521452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541603 | GGGGATTAGGCAGTT[C/G]CCTTCTGTTCCTAGA | 8945 |
rs529537082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375197 | GGGGCGGATTTCCGC[C/G]TTTTGTGCTGTTTTC | 8945 |
rs529546710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368128 | CGTTCCTCATGAAGG[A/G]CTTGGTGCCATCCTT | 8945 |
rs529549753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432517 | TTTTTTTGTTTTGTT[C/T]TGTTTTTTAACCTTT | 8945 |
rs529551410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482298 | AGTGCTGGGATTACA[C/G]GTGTGAGCCACTGTG | 8945 |
rs529601997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538226 | TGCCATGAATTTCTG[C/T]TATTCTTCCCTGCCT | 8945 |
rs529602054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528702 | TTTTCTTCCCTTTTT[A/T]AAAAAAAAATTTACT | 8945 |
rs529608328 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453009 | AACACACACACAGTG[-/T]TTTTTTTTAATGTCA | 8945 |
rs529611365 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101356913 | AGGCAGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 8945 |
rs529642664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411698 | TTAATTTTTAGGTCT[G/T]CTAATTTCATTGTCA | 8945 |
rs529650629 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101451718 | TTAATCAATAGGCAC[C/G/T]GTATGGCAGAGGGTC | 8945 |
rs529651672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428735 | GGATAATGTATTAAG[C/T]GTAGTCCTATGGGTG | 8945 |
rs529657653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371783 | ATTTAGCTCTGCAAT[C/G]CATCTGGAATTAATT | 8945 |
rs529705909 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101412435 | CATTCTGGCATTGTT[G/T]GTTGTTCAGTGTCTT | 8945 |
rs529711986 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101390018 | CTTTATATCTCAGTT[C/G]TAATCACCTACTTAG | 8945 |
rs529737129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520884 | ATCGCTTGATTCTCC[A/G]CCTGGGAGGTGGAAG | 8945 |
rs529738294 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101385168 | CCTCCGCTGCATTCC[A/G]GCCTGGGACACAGAG | 8945 |
rs529756499 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101461582 | TTTTAGGACCCAGAC[G/T]TGGAGATCTGTGCCA | 8945 |
rs529771864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364084 | TATAGTGACAGTAAT[C/T]TACTGCAGTGATCTA | 8945 |
rs529782899 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101470090 | TCATGTGCTTATTGG[A/T]TATTCAGACATTTTC | 8945 |
rs529803194 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365136 | TGGAATACAATGGCG[C/T]GATCTCGGCTCACCG | 8945 |
rs529811515 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101542738 | ACCACGTCCAGCTAA[-/T]TTTTTTTGTATTTTT | 8945 |
rs529825822 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396897 | AACCTCCGCCTCCCG[G/T]ATTCAAGCAATTCTC | 8945 |
rs529827271 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101483532 | TGGGAGGCAGAGGTT[A/G]CAGTAAGCTGAGATC | 8945 |
rs529830317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552850 | CCCACCCCTGCCCTG[C/G]CATTCTACAGGGCAA | 8945 |
rs529854521 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101548995 | GAGGCGGAGGTTGCA[A/G]TGAGCCAAGATCGCG | 8945 |
rs529868678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386815 | GGGGGTGTTTTTAAT[A/T]AGTACTTTTGTGATT | 8945 |
rs529880401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544932 | GGTGGCACGTGCCCA[A/G]TGCAACAACTTTTGG | 8945 |
rs529912808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444632 | ATTACACAAAATACA[A/C]TGCAAGCAGAAAACA | 8945 |
rs529941851 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101368610 | TTAGCCTCCTGAGTA[A/C]CTAGGACTACAGGCA | 8945 |
rs529947070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371191 | TTTGTTTGGTGTTTT[C/T]TTTTTCCCCCAGAGA | 8945 |
rs529949770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435621 | TTTGGATTGTTTCCA[A/G]TTTTGGCCTATTATT | 8945 |
rs529957862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537346 | CAGCCTGGCCAACAT[A/G]GCAAAACCCAGTCTC | 8945 |
rs530016511 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555772 | AGAAACAGAGCTGAA[G/T]GTGTCCCCATTGTAG | 8945 |
rs530023326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545913 | AGGGGCCAGTTCTCC[A/G]AGAAGACCTAACAAT | 8945 |
rs530034263 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544568 | GTGCCACCATATCTG[A/G]CTAATTTTCTTTATT | 8945 |
rs530044142 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101518203 | AGGCGTGAGCCACCG[C/T]GCCCGGCCGAAGTAG | 8945 |
rs530048852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485878 | AAGAAGAAAGTTCTT[C/T]ATCAAGAATTGACTG | 8945 |
rs530063648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486956 | TCATTCTGAAACATA[C/T]TGTGAATATCTATGA | 8945 |
rs530071011 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101438290 | ATTAGCCGGGCGTGG[A/T]GGTGGGCGCCTGTAG | 8945 |
rs530113298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421918 | GCTATTGTGAATAGT[A/G]CCACAGTAAACATAC | 8945 |
rs530115717 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | BTRC | GRCh38.p7 | 10:101418341 | CCACTGCACTCCAGC[C/G]TGGGTGACAGAGCAA | 8945 |
rs530134607 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101491125 | TAACTTAAATAGTCA[A/C]CTGCCTTATTAACAT | 8945 |
rs530134669 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520310 | TCCTCACCTTTGCCT[C/T]CCAAAATGCTGGGAT | 8945 |
rs530147228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539484 | CCTCTGTCACCCAGG[C/T]TATAGTGAAGTGGCA | 8945 |
rs530147313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380210 | CTCCTTGAGTCTCAC[C/T]TTCCTCATATAGAAA | 8945 |
rs530158028 | snp | G/T | 9.98037e-05 | 0.00706342 | intron-variant | BTRC | GRCh38.p7 | 10:101430469 | TACTTTCTCTGTCTC[G/T]GTGGGTTATTTGCGG | 8945 |
rs530186166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101430764 | ATAGCAGTTCAATAC[A/G]TAATATTTGCTCTGG | 8945 |
rs530205770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381028 | CAGTGTTATAATTTT[A/T]TGAGACCACTGTTGC | 8945 |
rs530206418 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432887 | TTACCAACCATGAAA[-/T]TGACCTGAGCCTTTG | 8945 |
rs530209095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403890 | GTGAGCTACTGCACC[C/T]GGCCCATTTAGTTCT | 8945 |
rs530210558 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101372665 | AGGTCAGGAGTTGGA[A/G]AACAGCCTGACCAAC | 8945 |
rs530214648 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101390335 | ATGTCCTGGTATGAT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs530232431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540166 | TTATGGCCTATGTTA[C/T]TTGCTGTTGTATCTC | 8945 |
rs530268723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395115 | TAATGTAGAAGTCAT[G/T]ATCACTAGGTGGCAT | 8945 |
rs530269365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404583 | TTTCTGTAGGATTGT[C/G]GTTTCAATGTCTGTT | 8945 |
rs530281129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387783 | CAAACTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 8945 |
rs530283972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521524 | ATTGCTAATAGAATA[A/C]CAGAGTGGGCTCAAT | 8945 |
rs530309412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101462225 | TGACATGGTTTTCCC[A/T]GTTATTTAAAAAACA | 8945 |
rs530326709 | in-del | -/CATT | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101525465 | GGGATATTTCCATGC[-/CATT]CTGTATTTCCTTCTT | 8945 |
rs530326960 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375200 | GCGGATTTCCGCCTT[C/T]TGTGCTGTTTTCGTG | 8945 |
rs530339037 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406407 | CTGACCTCGTGATCC[A/G]CCCGCCTCAGCCTCC | 8945 |
rs530339343 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101372417 | ACACCACCACGCCCG[G/T]CTAATTTTTGTATTT | 8945 |
rs530346677 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554728 | GTCAGGCAAACCCAG[C/T]CACTCGGAAGGCAGC | 8945 |
rs530347318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454604 | GGTAATATAGTGAGA[A/G]CCCCTGTATCTACAA | 8945 |
rs530356596 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101395535 | TTACAGACCCTTCCT[C/G]TCCTTAATAAAAATG | 8945 |
rs530369873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395972 | ATATGATGGGAGAAG[A/G]TTTTGTATTTTTGTT | 8945 |
rs530424130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441555 | CAAACTTCTTGAAGC[A/G]TCTTGCTTTTACTTT | 8945 |
rs530434550 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388655 | CCACCACGCTTGGCT[A/C/G]ATTTTTTTGCATTTT | 8945 |
rs530464929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551375 | TTTAAAAGGAATATA[A/G]AAAGTAGCTTTTATA | 8945 |
rs530480371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492259 | TTTGTTTGTTTGTTT[G/T]CAATGTGGGAGCAAG | 8945 |
rs530487922 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101418574 | AAATGACAGCATGAT[A/G]TACCTTGGCAATAGT | 8945 |
rs530500822 | in-del | -/A | 0.00958699 | 0.0685681 | intron-variant | BTRC | GRCh38.p7 | 10:101423470 | TTTACCTAAACTTAT[-/A]AGTAGCTGTTGTCTA | 8945 |
rs530541594 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101500315 | ATGGTGTTTGTGTAT[C/G]TAAACATTTCTAAAC | 8945 |
rs530546805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101491612 | TGAGGCAGGAGAATT[A/G]CTTGAACCCAGGAGG | 8945 |
rs530565021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433152 | GGTGAAGAGTAATTC[C/T]TCACTACACAGGGGT | 8945 |
rs530585412 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101483124 | GGACCCCTATAATAC[C/G]TTGATTGTAACTCTT | 8945 |
rs530592174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525351 | TTTTGCCCAACTGTC[A/G]TTTAGGTTTTATAGC | 8945 |
rs530601862 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423098 | TTTTTCATAAAAATA[G/T]AGATGGGGTCTAGTT | 8945 |
rs530603285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466343 | AGTGTTTAGGTTTTT[C/T]TGTATTCTTTCTCTT | 8945 |
rs530612179 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101375927 | GTGCTGGCCAGTGTA[A/T]CAACACAGGGGAAGT | 8945 |
rs530624266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376501 | ATAAGCAAGCTGTGA[C/T]ACTTAGAAGAGGTAT | 8945 |
rs530629369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517622 | CCATCAAATTACTTT[C/G]AAAAGTACCCAGTTG | 8945 |
rs530645138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543019 | GTAGCTGGCATTACA[A/G]GCACCTGCCACCACA | 8945 |
rs530649723 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101362207 | TGTGATTCGCCCGCC[G/T]TGGCCTCCCAAAGTG | 8945 |
rs530685416 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101458424 | CATTTTTTAATGGCG[G/T]TGTTATACAACTGTA | 8945 |
rs530688520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449155 | ATGGTTTTACGTCTC[A/G]GGATATTAGCTTTTA | 8945 |
rs530706037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516898 | CACCCAACTCATGTC[C/T]ATTTCCACCTTTTAA | 8945 |
rs530721520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449752 | TTTAATTCATTTTGC[C/T]TTGCGTATTTCTCTA | 8945 |
rs530726929 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362638 | GACCTTAGGTGATCC[A/G]CCCGCCTCTGCCTCC | 8945 |
rs530732329 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101507786 | AGTGCAGAGGCACCC[C/T]GGGTATGTCTGTGCC | 8945 |
rs530740207 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353658 | TTCAGCTTCCTAAAA[C/T]CACAGTTAGGCAGGT | 8945 |
rs530776636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355065 | AAACATGGGTACAGG[A/C]GATTGGGGCAAAATG | 8945 |
rs530777156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101399154 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCAAGCTG | 8945 |
rs530786538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519114 | ATGGAGTTTCGCTCT[C/T]GTTGCCCAGGCTGGA | 8945 |
rs530789224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391444 | TGTCTTAGGTTAATA[A/C]ATTGTCTCTGAGTCA | 8945 |
rs530819844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510681 | AGAACACTGTTGTAT[C/T]CCCATCCAGATTAAT | 8945 |
rs530821805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508822 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 8945 |
rs530823386 | in-del | -/CTA | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101552680 | ATAGCAAGAGCACTT[-/CTA]CTAGTGCTCACATCC | 8945 |
rs530852184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401965 | TATTGTCTTATGCTC[C/T]GGAGTTCTTACCTCA | 8945 |
rs530880460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101451840 | TGGGAAGAGCCTGCC[A/G]CTCAGGGGCTTTGTG | 8945 |
rs530929660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101385748 | ACACACACACACATA[C/T]GTTTTGTACAAAATT | 8945 |
rs530950535 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551484 | GTCTCCAACCTCTCT[C/T]TCAGGCAGGGGAAGA | 8945 |
rs530952644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | BTRC | GRCh38.p7 | 10:101516009 | TCTGGGTGTTGGTTA[C/T]GTGAGTATGTTCACC | 8945 |
rs530976014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101369501 | CTTGTTTACTGAAAG[A/G]TACTCCAGGCTCTTC | 8945 |
rs530990579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475077 | ATGTTTGTGGAATTA[C/G]ACAACGCAAAAGAAA | 8945 |
rs531000993 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101538873 | ACCAACACGGTGAAA[C/T]CCCATCTCTGCTAAA | 8945 |
rs531042121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452420 | GATTGGAATTCTCCT[A/G]TCCAAGGCTTCCATT | 8945 |
rs531052349 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101552059 | CCTTAGACTTCCGTG[A/T]TACTTTGCCATTTTT | 8945 |
rs531052354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394212 | TTTTTATGATAATGT[A/G]TTCTTTCAATTTGGA | 8945 |
rs531066619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101493597 | TATTGAATGTTAACA[A/G]TTTACTAACAACTAG | 8945 |
rs531067708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475851 | CATGATTAGCACCCA[A/G]TGGATGCTAAAATTA | 8945 |
rs531077989 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101467420 | AGCCAAGGGAGCTTT[C/G]TTCTGATAATTGCTC | 8945 |
rs531078733 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490265 | TCCCTCCCTTCCTTC[C/G]TTTCTTCTTCCTTCC | 8945 |
rs531085239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535636 | CAGGCAGAGAAGCAG[C/G]ACAGCAAAGCCTTTT | 8945 |
rs531087647 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101362153 | TTTAGTAGGGATGGG[G/T]TTTCACCATGTTGGC | 8945 |
rs531097943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527490 | GGGTGGGGTGGCTCA[C/T]GCCTGTAATCCCAAC | 8945 |
rs531111413 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486710 | TTTTATAAAATGGTC[A/G]TACTCAAGACAAGCC | 8945 |
rs531118477 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101400958 | CCCACCGAACACTGC[A/T]ATCATTTGAAATTTG | 8945 |
rs531118648 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101429693 | CCCTCGCCTTATACC[C/G]CCCACCCCCCACAGA | 8945 |
rs531168800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358513 | TATTGTTTTATTTAT[A/G]GAGCTGATAGATAAA | 8945 |
rs531178616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536260 | TTCTCAGGCAACTGC[A/G]TGCATTGAATTCGTT | 8945 |
rs531179494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526610 | CGTGGCGAAACCCCA[A/C]CTCTACTAAAAATAC | 8945 |
rs531179640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514422 | GACTTCATTTCCTCT[A/G]TGGATATCCAATTGT | 8945 |
rs531188727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404821 | GGCTAATATGGTGAA[A/T]CTCCATCTCTACTAA | 8945 |
rs531215595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515280 | ATTTTCAGGAATATT[C/T]TGGTTAAGTTTAGGT | 8945 |
rs531216064 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553171 | ACCCATTAAAGTTGC[A/G]GTATTTAACGTATCT | 8945 |
rs531279745 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101477170 | TTTTTATTTTCTTTT[C/T]TTGTATTTTTAGTAG | 8945 |
rs531284128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101516029 | GTATGTTCACCTTGT[A/G]AAAATTAGTTGAGTA | 8945 |
rs531286569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362537 | AGTAGCTGGGATTAC[A/G]GGCATGCGGCACCAC | 8945 |
rs531301789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506183 | CTCCCAAAGTGCTGG[A/G]GTTACAGGCGTGAGC | 8945 |
rs531309049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522676 | TTCACCCGCCTTGGC[C/T]TCCCAAAGTGTTGGG | 8945 |
rs531319255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463538 | CAGCAGTAAAAATAA[C/T]TCTAATTTACTTGGA | 8945 |
rs531325521 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101374963 | AGATCTGCCAGTTAA[A/G]GAGGCACAAAGCTAC | 8945 |
rs531339583 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101497521 | GGTCAACAAAGTGAG[A/G]CCCCTGTCTCTACAA | 8945 |
rs531347177 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472596 | AGGTTGGGTGGATCA[C/G]CTGAGGTCAGGAGTT | 8945 |
rs531405181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455633 | AAAGAAGCCTGTTAC[A/G]TGTTAAGGGACTAGA | 8945 |
rs531422611 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525427 | CATTCTTGAACTTAA[A/G]CATACATCTCTGTCT | 8945 |
rs531445750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447247 | ATCCAGGCCCTCGTG[A/G]GTCAAGTGACCCACA | 8945 |
rs531454012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530896 | TATATAATGTCGGCC[A/G]GGTGTGATGGCTCAC | 8945 |
rs531461003 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101479853 | CAACCCAATTATTAT[A/G]TCACTATTATTATTT | 8945 |
rs531487930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365205 | TAGCTTCCTGAGTAG[C/G]TGGGATTACAGGCAT | 8945 |
rs531490175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429411 | CCATATGTATTATAT[A/G]TATGTACATTCTTAG | 8945 |
rs531496571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539401 | TTCTTGGCTCTGGAG[A/G]AGAGAAAGAGGTTAC | 8945 |
rs531521175 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101374865 | CTGGACCAGCTGTAC[C/T]CAAATTGTTATGTGA | 8945 |
rs531544777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471966 | CAGGCTTCCATGCCC[C/G]CTTTGACGTATCTTC | 8945 |
rs531551384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101462477 | TGAAGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 8945 |
rs531555368 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101365888 | AAAACAAAATGATCA[A/T]GGACTACATTGTAGC | 8945 |
rs531559870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532662 | GAAATGCACTGAATG[G/T]GCTGTTACTCTTTTG | 8945 |
rs531565304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432307 | ATTTTTCTATTTTTT[C/T]TGTGGAGATAGGGTT | 8945 |
rs531579428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375180 | GAGGTGTTTGGATCA[C/T]GGGGGCGGATTTCCG | 8945 |
rs531581058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421706 | CAATTCCCACCAAGA[G/T]TGAGAACGTGCAGTG | 8945 |
rs531583143 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101378134 | ATTTAGATGGAGGCA[A/C]GGAAGGCTTTCCCTT | 8945 |
rs531584130 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101409178 | TCTATGTAGTTGAAA[G/T]ACATTTACATCATTC | 8945 |
rs531585046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101540063 | CAAGTATTTTCTCCA[C/T]GTTCATAAAATTTGT | 8945 |
rs531600101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415272 | CCTCCACATTCCAGG[C/G]TGAAATGATCCTCCT | 8945 |
rs531603543 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101413345 | TTTTGACAGAGTCTC[A/G]CTCTGTTGCCCAGGC | 8945 |
rs531605033 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101526595 | GACCAGCCTGGCCAA[A/C]GTGGCGAAACCCCAA | 8945 |
rs531618756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422505 | ATTTTGGCTTTTGTT[A/G]CTATGGCTTTTGGTG | 8945 |
rs531642585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533222 | GTCAGTCTAGAACTA[C/G]AAAACTTGATTTAGA | 8945 |
rs531698254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368009 | GTTTAGCTTTATGCT[A/G]TGGTTTGAATATAGC | 8945 |
rs531705503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367304 | CTATCTCTTGACCTT[G/T]TGATCTGCCTGCCTC | 8945 |
rs531759170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472837 | TTATATCGTTACTCC[C/T]AGATACCTAACATCC | 8945 |
rs531797011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473672 | GATGGGGTTTCACCA[C/T]GTTTGCTAGGCTGGT | 8945 |
rs531819959 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101524475 | AATCTAATGCTTTAT[C/G]GCCATTTAAACTTAT | 8945 |
rs531821435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390583 | GTGATCCTCCCGCCT[C/T]GGTCTCCCAAAGCGC | 8945 |
rs531827962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359453 | GTCTGAGATACCCTG[A/C]GTCTCGCTCTGTTGC | 8945 |
rs531839014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412225 | TTGGAACCTTTTTCT[A/G]CATAATTCATTCTTC | 8945 |
rs531843345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382052 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTT | 8945 |
rs531850022 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409014 | AGATTGTGCCACTGC[A/T]CTCCAGCCTGGGCGA | 8945 |
rs531877669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465170 | TGTCAAGGCCGCCTT[A/C]TACCTAGTATTGATA | 8945 |
rs531880342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381833 | GCATGTATTTTCTAA[C/G]AACAAGAGCATCCTT | 8945 |
rs531882630 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101519224 | CTGGGATTACAGGCA[-/C]CCCGCCACCACACCT | 8945 |
rs531904539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101541280 | CTTTTTTTTTTTTGA[A/G]ACGGAGTCTCGCTCT | 8945 |
rs531913807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549595 | GGCAGGCGCCTGTAG[C/T]CCCAGCTACTCGGGA | 8945 |
rs531918205 | in-del | -/GATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101422226 | CTGATGGCCAGTGAT[-/GATG]AGCATTTTTTCATGT | 8945 |
rs531928121 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352198 | TAGTTTTCATACGAA[C/T]GCGTTTGAAGTCTTC | 8945 |
rs531937824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101498209 | CCCAGGCTGGAGTGC[A/G]GTGGCGTGATCTCAG | 8945 |
rs531938878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427158 | GAGTCTTGTTCTGTC[A/G]CCAGGCTGGAGTGCA | 8945 |
rs531940018 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101480811 | AGTTAAATGTCTCAA[A/G]TCCAAATATGTTAAT | 8945 |
rs531943164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490449 | TTTACAAACGAGGAA[C/T]GAGAAGCTTAGATAA | 8945 |
rs531952530 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101446590 | AAAACAGTTGATGCT[A/G]TGTATATTTCATTTT | 8945 |
rs531986228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370505 | GGCCCTGACAAAATG[A/C]GTAGAGGTTTATTGT | 8945 |
rs532024741 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101489461 | AATATTCTCCTCTCT[C/T]GTTTGACAGTTTCAA | 8945 |
rs532036516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537293 | AGCACTTTGGGAGAC[C/G]GAGACAGGTGGATCA | 8945 |
rs532041569 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101374459 | ATGCAGCCATAAAAA[A/C]TGATGAGTTCATGTC | 8945 |
rs532058789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101419302 | AGGTGTGAACCACTT[C/T]GTCTGGCCAGTACCT | 8945 |
rs532093862 | snp | C/T | 3.31455e-05 | 0.00407083 | intron-variant | BTRC | GRCh38.p7 | 10:101536508 | GCTTAGAAAAGAATA[C/T]GTGAAAATTCACCTG | 8945 |
rs532097946 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400747 | CAACTGCTATGAACA[A/G]ACATGTAAATCCATC | 8945 |
rs532102600 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101377953 | ATAGGATGACCAAAA[A/T]TTTTTTTATATGCCT | 8945 |
rs532122954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528631 | TTCCTCCATTATTCC[C/T]TCGACTTTCTTGTTG | 8945 |
rs532122977 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101384405 | GATTAGTGCCAGTAC[G/T]TGCAGGTAGATACTT | 8945 |
rs532152279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101551664 | CCTCAGTTCTCGTGG[C/T]GGAAGTACATGTTCG | 8945 |
rs532155999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469097 | ATTAAAGTACTCCAA[C/T]GCAAAACTCTCTGCC | 8945 |
rs532159678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485141 | GTAAACAGGAATCTT[G/T]GTCTGTGTTAAAGTT | 8945 |
rs532167443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101476092 | AGAGGGGCACATCAC[C/T]TCTAAAGTATCTTTC | 8945 |
rs532181267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527588 | TGAGACCTCATCTCT[A/C]CAAAAAAATCAAAAA | 8945 |
rs532191590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468463 | AAAAAAAATCTGCCC[C/T]AAAAACAACACGGAA | 8945 |
rs532196319 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101378848 | TCCATGGGAAAACAT[C/G]CGCTTTGAAGCAGTA | 8945 |
rs532204961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477168 | TTTTTTTATTTTCTT[C/T]TTTTGTATTTTTAGT | 8945 |
rs532207106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393674 | TCACAGAGAAGTCTT[A/C]TGTGTTGATGATTAT | 8945 |
rs532217140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371061 | TTCACACTGTTTTGC[A/T]TATATAATCTTTAGA | 8945 |
rs532240726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101443340 | TGCAAATGTAGTCCT[A/G]CGCAACATTAAAAGC | 8945 |
rs532254510 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101368933 | CTGACGCACGAGAAT[C/T]GCTTGAACCTGGGAG | 8945 |
rs532292467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355301 | AAGTCAGGATTTGTG[A/G]TTACCCGTCAGTTTT | 8945 |
rs532303915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500850 | GTTTGACCTATTCTT[A/G]GGGTTATAGAATATC | 8945 |
rs532316950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377236 | CATGTATCAGGAGTT[C/T]ACGTCTTACTATTGT | 8945 |
rs532324731 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520872 | TGAGGCAGGAGAATC[A/G]CTTGATTCTCCGCCT | 8945 |
rs532325086 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101434791 | CATGGCTGAAACCCC[A/G]TCTCTACTAAAAACG | 8945 |
rs532331151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442651 | AAAAAAAATCGAGTT[C/G]GTGGGTCATCTTTTT | 8945 |
rs532344368 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101451728 | GGCACCGTATGGCAG[A/T]GGGTCAGTAATCAGT | 8945 |
rs532368891 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101390680 | TTTTTAAAAGACATT[A/G]GAGCAAATTTGAGAA | 8945 |
rs532379991 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553982 | GTGGATTCTCAGACA[C/T]GATACTCTCATCATA | 8945 |
rs532382792 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101367782 | GTTGTGGGAGGTGTG[A/G]TGTGTTTATTCTTGT | 8945 |
rs532407003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495423 | ATAGCAACAATTAAA[A/G]CAAATTAAAAATAAA | 8945 |
rs532415185 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497491 | GGATTGAGCCTAGGA[G/T]TTTGAGACCAGCCTG | 8945 |
rs532432696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436970 | AGGAATATGGATTAT[C/T]GAATTGAATATACAT | 8945 |
rs532435824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101376778 | AGGTCATAGGGTAAG[A/G]TGGTGGTGGTGGTGG | 8945 |
rs532462067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486140 | AAAATTACTGCTAAC[A/G]CTCAGAGATCGGCAG | 8945 |
rs532478116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484538 | ACTTCCTCTGGGTCT[C/G]TGCTATTTATAAGGC | 8945 |
rs532501938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478249 | GAGGTTGTAGTGAGC[C/T]GAGATTGTGCCACTG | 8945 |
rs532504708 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465106 | ATTTTGTTTTTTTGT[C/T]TTTGTTTTGTTTTGT | 8945 |
rs532508949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371930 | GAAAACCCAATCGTC[A/G]TGCTTACAAACTACA | 8945 |
rs532520665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428880 | TGTGCTGCCCAGGCT[A/G]GATTTGAACTCCTGG | 8945 |
rs532524865 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101505777 | GTCTACTGTAAATGC[-/T]ATTTTTAGAAAATGA | 8945 |
rs532564647 | in-del | -/GC | | | intron-variant | BTRC | GRCh38.p7 | 10:101408603 | GAGTCACTGGGCCTG[-/GC]CCTTTTTGCCTTTAA | 8945 |
rs532577797 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554522 | CTGCTTCTCCCACAC[C/G]CAGTATTTGCAGAAG | 8945 |
rs532584565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387752 | TGAAGTGCGGTGGCG[C/T]GATCTCTGCTTACTG | 8945 |
rs532629697 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530771 | AGGTTACTCTTTGAC[A/G]TGGGACTCCTGAAAT | 8945 |
rs532641350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403156 | CCTGAGGTGTCTTCT[C/T]TGGGGACGATACACA | 8945 |
rs532646970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388261 | CAACCTCCTGGGCTC[A/C]AGTGATCCTCCTGCC | 8945 |
rs532650471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380042 | AACTGACAATACGAG[A/T]ATTCTACCTGTTTTG | 8945 |
rs532662889 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473845 | TCAAGCTATCCTCCT[G/T]CCTCGGCTTCCCAAA | 8945 |
rs532676704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547114 | AATAGGTTAGGCAGA[C/T]CAAATGCATTTTCAG | 8945 |
rs532677533 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101453626 | TTTATTTGATTATAT[A/G]ATCAACTCTTAATTA | 8945 |
rs532697774 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378186 | CCATCTATCTCTTCT[C/T]CTTTGTAGATCATCC | 8945 |
rs532703013 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101408116 | ATGGGTATTTTAAAG[-/TT]TTGTAACATATTTCA | 8945 |
rs532704868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101520175 | GGGGGACAGAGTCTC[A/G]CCCTGTTGCCCAGGC | 8945 |
rs532707126 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101375725 | TTGTAATAGTTCTAC[A/C]CTTTACCCTGTATAG | 8945 |
rs532775010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356622 | TTACTTTCATTATTG[A/G]CCTTGCCTGCTGTTT | 8945 |
rs532780704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520800 | CTGTCTCTACTAAAA[A/G]TATAAAACTTAGCCA | 8945 |
rs532794773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512162 | TTGATTGATACCACT[A/G]AAGTTCCAGGTTTAG | 8945 |
rs532813028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394543 | AGCAGGTCCTTCTTC[C/T]GCTTCCCTACTCCAC | 8945 |
rs532816357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461475 | TGGACTCTAATCCTA[A/G]ACTACTGAGTAAATG | 8945 |
rs532820703 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101503711 | TTAACATGCATTAAC[A/C]AGCATTTGAAAAGAG | 8945 |
rs532853026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490575 | CAGGTAGTATTTGGA[A/G]GCCTCTGCACCTCTC | 8945 |
rs532875636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499394 | ATGCCCAGCTAAATT[C/T]TTTTGTATTTTTAGT | 8945 |
rs532877002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101387145 | ATTTATATCAGTGCC[A/G]TACTATCTTATTCAT | 8945 |
rs532891707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482456 | GTTGGAGTGCAGTGG[C/G]ATGATCTCGGCTCAC | 8945 |
rs532891720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491463 | ACTTTGGGAGGCTGA[A/G]GTGGGAGGAACACCT | 8945 |
rs532900615 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101441473 | TCATAATGTAGAAAT[C/G]CTTTATGAAATGTGT | 8945 |
rs532904781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507613 | ATATTTTACATAAGC[A/G]CTGGGAAAATGTCTT | 8945 |
rs532977318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101473800 | ACAGGATCTCACTAC[A/G]TTGCCCAGGCTGGTC | 8945 |
rs532994770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391185 | ATTCAAATATTTCAG[C/T]CCTTAAGCAGTTATA | 8945 |
rs532997089 | in-del | -/GTTTA | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101460068 | CACTGAATTAAACAG[-/GTTTA]GTTTATCTGATCTTT | 8945 |
rs533030493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457024 | AACTCCATGTATACT[A/G]TGTTTTTTCCTATGG | 8945 |
rs533052435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465018 | ATTTTTTTTAAGGTA[A/G]GACATAGTATATAAG | 8945 |
rs533055001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375266 | TGTGGCACCTTCTCT[A/G]CCCCCCTCTCTTCCC | 8945 |
rs533058315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101506867 | GTTTTTGAAAAGAGA[C/T]CTAGGAATTCTGCAG | 8945 |
rs533059432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101457982 | CACACGCACATACAT[C/T]CATTTATGTATTATT | 8945 |
rs533065732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432563 | GTTTAGGCGATCTGC[A/C]AAGTCTGAGGGAATT | 8945 |
rs533073413 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101368127 | GCGTTCCTCATGAAG[G/T]GCTTGGTGCCATCCT | 8945 |
rs533083427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550559 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACTGCG | 8945 |
rs533106828 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352938 | GGCCAGGCTCGTCTC[C/G]AACTCCTGACCTCAG | 8945 |
rs533112266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523596 | AGAAAATATTTAAAA[A/G]CATTTCCTAGAACCC | 8945 |
rs533113568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101362108 | TGGGATTACAGGCAC[A/G]TACCACCACACCCAG | 8945 |
rs533116693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359383 | TCTGGGTACTCTTAT[A/G]GGTGTTGGGGTATGA | 8945 |
rs533125459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526509 | TGTGGCTGGGCACAG[C/T]GCGTTCACGCCTGCA | 8945 |
rs533134326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415145 | CAACCTCCATTCATG[A/G]TTAAGTGCCCTATAT | 8945 |
rs533136259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464379 | GGGACTAATCTGATT[C/T]ATTTTAAAAATAAAT | 8945 |
rs533143007 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386649 | GAGCACATGAAGAAC[C/G]AAGGACTTGTTTGAC | 8945 |
rs533170228 | snp | A/T | 0.0136579 | 0.081501 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352129 | TTTATTTATTTATTT[A/T]TTTTTTTTGTAACTC | 8945 |
rs533188802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354296 | TCGCTGGCCTGGGCC[G/T]CCCGCCCACTGCGGG | 8945 |
rs533193105 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101518411 | TTTCTTACATGGTAG[C/T]TCAGCGCTCTAAGGA | 8945 |
rs533199696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407019 | ACATTTACCACAGAT[A/G]CCAACCAAGTATATA | 8945 |
rs533200467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524353 | GTTACTATCTCAAGC[C/T]TATACCACTAAGAAT | 8945 |
rs533210939 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447499 | TACTTTAATACCACA[A/G]TTAGCTATTATGGTA | 8945 |
rs533217206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409710 | AGTTAAAATGTTGGT[A/G]TTATCATCTGTGGGA | 8945 |
rs533233022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509945 | GGCCAAGACAGGTGG[A/G]TCACGAGATCAGGAG | 8945 |
rs533235749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383190 | CACCTCAGCCTCCTT[A/T]GTAGCTGGGACTACA | 8945 |
rs533238245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516811 | ATAAGTGGAATAATT[G/T]CATTAAGCTGCTGAT | 8945 |
rs533270278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392959 | TGTTAGGCCTCAGCC[A/G]CAGACCTCAGGAAAT | 8945 |
rs533284989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390840 | CTCTCTTCTTTCTAA[C/T]TTTCCTGTCCCAAGC | 8945 |
rs533286918 | in-del | -/CTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101537709 | AGTGTAGACTGCTCA[-/CTT]CTTCTGCTTTGGGAC | 8945 |
rs533289218 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101399117 | GCCACCATCCCCGGC[C/T]AATTTTTTTGTATTT | 8945 |
rs533300629 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101413156 | TTGAGATGGAGTCTT[A/G]CTCTGTCGCCCAGGC | 8945 |
rs533313212 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353856 | ACAATTCCCATCAGC[C/T]GATTTCCTCTGCGTA | 8945 |
rs533318486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101433034 | CACATTTGTCCAGTC[A/G]CTAAATCTCTCAGGC | 8945 |
rs533320830 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101368164 | AATAAGTGAGTTCTC[G/T]CTCCATTAGTTCCTG | 8945 |
rs533324616 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101509060 | TGTAAAAGGATGCTC[A/G]GGTGCCAATGGGCGC | 8945 |
rs533371397 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101541850 | TCTTTTTAAGGATTT[G/T]TGTGTGTGTGTGTAT | 8945 |
rs533430596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368817 | TGAGGCCAGGAGTTC[A/G]AGTCTAGCCTGGCTA | 8945 |
rs533476588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450742 | TGCCCCCCAGGACTC[A/G]TAAGTAAACAAGGTG | 8945 |
rs533490336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361350 | TGACCTTGTGATCCA[A/G]CCGCCTCAGCCTCCC | 8945 |
rs533503304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474883 | TGTAGCTTTAAAATG[A/T]TTTTCCTATCTGCAA | 8945 |
rs533550133 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453008 | AACACACACACAGTG[-/T]TTTTTTTTTAATGTC | 8945 |
rs533554687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542417 | GCCACATCCCAAAAA[A/G]TGTCAATTAAGTCAA | 8945 |
rs533593568 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358622 | CCCTCAAATCTGATG[A/G]TTTTTCTGCTTCACT | 8945 |
rs533594086 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553659 | AGCCCCAATATGCTT[A/T]GGAGGAGACAGAGTT | 8945 |
rs533594886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504143 | CTGGTAATCTTAACA[C/T]AATTTGACATCTAGG | 8945 |
rs533599455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534587 | AATATAAGGGGTGGA[A/G]GGGCGCATGATGGTC | 8945 |
rs533623427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445069 | GTTAGGGTTTAGTTA[C/T]CGACATTTCATTTGA | 8945 |
rs533636734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474414 | CATCCCTCTAACTTG[A/G]TAGAAGTCAAACTCT | 8945 |
rs533651980 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101447962 | GATAGTAAAATTTTC[C/T]ATAATTCAGTGACTT | 8945 |
rs533659089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101436382 | GGGCACGGTGATGCA[C/T]GCTTATAATCTCAGC | 8945 |
rs533666954 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463148 | CCTCCAGGGTTCAAG[C/T]GACTCTTCTGCCTCA | 8945 |
rs533703182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418825 | ATCAAGCCCAGCATG[C/T]ATCAGCTCTTTTCCC | 8945 |
rs533707968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362959 | TATGGGAGGATGTGT[C/G]TAGGTTATGTGCCGT | 8945 |
rs533725646 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101431947 | AATCAAGTCTTGAAT[A/G]TTGTCTTTGTCACTA | 8945 |
rs533727540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101527973 | GTTATATGGTATTCG[A/G]GGTCCATCATTTTGC | 8945 |
rs533729127 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101466541 | TCACCTGCAGTGAGG[G/T]TTTACATTGATTAGG | 8945 |
rs533751360 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101466116 | CAACTCTTTGCTTCT[C/T]ATTGGTGCTAATAGG | 8945 |
rs533753994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453079 | TAAAATATCTGTTAA[C/T]CTTGTAAAATAATAA | 8945 |
rs533763573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528839 | TTCCATTTCTACTAA[C/T]CAAAAATAGTAAGTA | 8945 |
rs533765272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519734 | GGTGCAGTGGCTCAC[A/G]CCTGTGATCCCAGCA | 8945 |
rs533771332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468685 | GTCACTAACGATTTT[C/G]ATTATACTATATCTT | 8945 |
rs533778406 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460872 | AACGTTATGACTATA[G/T]GTAATGTAAGGAATA | 8945 |
rs533810828 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457970 | TAAATACATATACAC[A/G]CGCACATACATCCAT | 8945 |
rs533828222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355471 | GCTTTTAATCTGATG[C/T]TTTTTGTATTTCCTA | 8945 |
rs533848566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520323 | CTCCCAAAATGCTGG[A/G]ATTACAGGTATAAGC | 8945 |
rs533888622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422112 | AAGTGTTCCTCTTCT[C/T]CACATCCTCTCCAGC | 8945 |
rs533889717 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101445709 | TAATCGCTTTGGTTT[A/G]ATCAATAGAATAATT | 8945 |
rs533912652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357083 | GCAGTGAGCCAAGAT[C/G]GCGCCACTGCACTCC | 8945 |
rs533913104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387889 | GAGACGGGGCTTTGC[C/T]ATGTTGGTCAGGCTG | 8945 |
rs533950818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368848 | ACGTGGTGAAACCTC[A/G]CTTCTACTAAAGGTA | 8945 |
rs533970134 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363918 | TCAGTTAGCTATTGG[C/T]GTTTAGAATCACAAA | 8945 |
rs533999786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101529265 | TCTGTAACACTTTGA[C/T]TTGAAGAAATTCAGA | 8945 |
rs534004759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432154 | TTTTTTTTTGAGACA[A/G]TCTTGCTCTGTTGTC | 8945 |
rs534016113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477346 | AGATGATTCTGATGC[A/G]CACTAAAGTTTGATA | 8945 |
rs534039777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460640 | GTGTCAGCCACAGAG[A/G]TGAAAGGGCCTCAGA | 8945 |
rs534074499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463802 | TTCTGACTTCAGTTT[A/G]TATATAGTGTTTAGA | 8945 |
rs534076566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455118 | CCAGGCTAGAGCACA[A/G]TGGCATGATTACACC | 8945 |
rs534103103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546528 | CACAGCTATCAAAAT[G/T]TGTGGGATGCAGTGA | 8945 |
rs534146371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379180 | ATTGCTTCCACTTAT[A/G]TCAGAGTTTGAAAGT | 8945 |
rs534153549 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101429070 | AGGAGAAAAAAGTCT[A/G]TGACAATATAAAATA | 8945 |
rs534154618 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101365365 | GGCGTGAGCCACCGC[A/G]CTTGGCCCTTTTTTT | 8945 |
rs534186900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547377 | AGTCTCACTCTTGTT[A/G]CCCAGGCTGGAGTAG | 8945 |
rs534221154 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101471357 | TCACACCACTGCACT[C/G]CAGCCTGGGCAACAG | 8945 |
rs534227378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530246 | TTAGACTTGATAGCA[C/G]TGCTCTTAGGCATTT | 8945 |
rs534239430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429683 | TTGTTTCTTCCCCTC[A/G]CCTTATACCCCCCAC | 8945 |
rs534283154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101358022 | AAAATGATTGAGGGA[A/G]TATAGACCCCAAAAC | 8945 |
rs534354294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495652 | AAATCTTTTTTATTA[C/G]AAGTCCCTGTTTCCT | 8945 |
rs534361315 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417249 | AAATATCTAGTTCAG[C/G/T]ATCACATGATACATT | 8945 |
rs534367148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467002 | AGGAAAAAGCACATC[A/G]CTGACACAGAAAATG | 8945 |
rs534380276 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101504549 | CACCAACCCCACTGC[C/G]TAGTATCCACTGTCC | 8945 |
rs534385366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374257 | AATGATTGCCATTCT[G/T]ACTGGTGTGAGATGG | 8945 |
rs534391398 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387451 | CACTGCTTTATAATA[C/T]ACCTTTTTTATGGTA | 8945 |
rs534394761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486313 | CGCATAAATCTGCCC[A/G]AATGGTGGGGGCTGG | 8945 |
rs534407406 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101400630 | TATTTGGCTGTTTTT[C/G]CCTGGGAAGTGAGGG | 8945 |
rs534449341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467436 | TTCTGATAATTGCTC[A/G]AGAAAACCCATTCCC | 8945 |
rs534495727 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539722 | GGTCATATGGTAAGT[A/G]TATGTTTAAAATTTT | 8945 |
rs534502332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440883 | AGATAATACTTGTAA[A/G]ATATAAGTCCTGCTC | 8945 |
rs534502898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372710 | TCTCTACTAAAAATA[A/C]AAAAATTAGCCGGGC | 8945 |
rs534506686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550154 | GGTTGGCCATGAGAA[A/G]CTATTAATAGCATGC | 8945 |
rs534507384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539666 | AATGTATGCTTTTTG[C/G]TTTTATTTCTCTGAG | 8945 |
rs534532743 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101508870 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 8945 |
rs534537538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432713 | ACTCACAGTTTATTA[C/T]AGGAAAAGGACACAG | 8945 |
rs534544666 | snp | A/G | 9.9425e-05 | 0.00705001 | intron-variant | BTRC | GRCh38.p7 | 10:101479482 | ATTGCTCATCAATGT[A/G]TATTACACCACACCA | 8945 |
rs534549898 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101383426 | AAGGCTAGTCAAGTT[C/G]TGAAGCAATTGGTTG | 8945 |
rs534580563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360851 | TTTATTTTATTTGGG[C/T]GCAGCTCTGCCATCA | 8945 |
rs534608216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416688 | TCAGCATCTTACTCT[C/T]TGCGTGTAAAATTTA | 8945 |
rs534617620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542610 | AGGGTATCACTATGC[C/T]GCCCAGGCTGGAATG | 8945 |
rs534632831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101368922 | TACTCAGGAGGCTGA[C/T]GCACGAGAATCGCTT | 8945 |
rs534648107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483150 | CTCTTTGCCAGAAAT[A/G]TCATAGTCTTATGAT | 8945 |
rs534664826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492977 | AACTGATTTTTTAGT[C/T]AGCAGTTTAGGTTGC | 8945 |
rs534679242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101409031 | TCCAGCCTGGGCGAC[A/G]AGAGCAAAACTCCAT | 8945 |
rs534689997 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481778 | AACATTATTCTGACA[C/T]CTATATCCTTTCGTC | 8945 |
rs534697245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493701 | GTTTTTCTTCTCTTG[C/T]ACTTATAGTATTTTC | 8945 |
rs534699045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101483979 | TTTTTTCCCTAATTT[A/G]CCCTTACCCACACCC | 8945 |
rs534727085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101518067 | ACAGGCGCCCGCCAC[C/T]ACGCCCGGCTAATTT | 8945 |
rs534729691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376980 | TTTCTTAATGTACAC[A/G]GTTTTAGGAATTCTA | 8945 |
rs534755591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415622 | TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCTGAG | 8945 |
rs534782443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484716 | ACTAAGATATAACCA[C/T]GTCATTGAGGCTGAT | 8945 |
rs534802271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370663 | CAGCCTTGACCTCCT[G/T]GGCTCAAGCGATCCT | 8945 |
rs534819893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449354 | ATTTTGTCATACGTC[C/G]TAAGGGTTCTATAGT | 8945 |
rs534868014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459657 | TTGCCCTAGTGGGAT[A/G]GAAAGGGGAAAGGAA | 8945 |
rs534882678 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101542818 | GGGCTCAACCTCGAC[A/G]AAGTACTGGGATCAC | 8945 |
rs534884871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101541853 | TTTTAAGGATTTTTG[C/T]GTGTGTGTGTATCTG | 8945 |
rs534886643 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101386043 | ATGACTTGGCTGGTA[G/T]TTATCAAAAATCCTC | 8945 |
rs534905710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482545 | GGACTATAGGCGCCC[A/G]CCACCACGCCCGGCT | 8945 |
rs534906109 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453446 | TTGGTGTGAAATGTT[C/T]GCTTGTAGCTTTGGA | 8945 |
rs534911261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375399 | ATCAGAAGCAGAATT[A/C]ACTACGCTTCTTGTA | 8945 |
rs534917415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533877 | CCTTGTAGTTACTGA[C/T]ATTTAACATTTATTG | 8945 |
rs534923379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368295 | CCGTGAGTGGAAGCC[A/G]CTTGAGACTCTTACC | 8945 |
rs534933927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376032 | AATTAACTGGAATCA[A/G]AAGTGATGGCAGGCC | 8945 |
rs534944978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510196 | TCAAAGGAAAATAAT[C/T]GGAAAAAGATCTTTT | 8945 |
rs534954284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474166 | CTTTTTCTCATTTTT[A/G]GTAATTTTTGATCAT | 8945 |
rs534982724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502364 | TTATGGGAAAACATT[A/G]TAGCAATAGCTCTGA | 8945 |
rs534983144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101501255 | AAGAACATGTGAAGA[A/C]TGAATCTCTATTTTT | 8945 |
rs534993651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543751 | TATCAGATGATATTG[C/T]ACCACTTCATGTATA | 8945 |
rs535006981 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481503 | TTTGTTTTCTCCATA[C/T]TTTGTAAGCCAGGAT | 8945 |
rs535008535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434501 | AGAAAATGTGGCAAA[A/G]ATAATCATTGTGACT | 8945 |
rs535011417 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101442790 | TACAATTTTTTTCCT[C/G]GTTGTTAGAAATAAG | 8945 |
rs535014825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552134 | CACTCCCAAGAGTCT[A/G]TTTCTGGCTTTTCTT | 8945 |
rs535031759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385234 | TAGCCGGGCGTGGTG[A/G]CGGGCACCTGTAGTC | 8945 |
rs535037635 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101438163 | AATATAAGTCTTCTC[-/A]CGTCTGTAATCCCAG | 8945 |
rs535049142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426786 | AAGTCTGTGAATGAA[A/G]GGGTTCTGGTTGGTT | 8945 |
rs535049219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434912 | AGTCCTGGGATTACT[G/T]GCATGAGCCACTGCA | 8945 |
rs535055183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506247 | AATTTTTTTACCTTT[A/C]AAAATGGGTGGCCCT | 8945 |
rs535057186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496864 | TGATGTATGTATTGC[A/G]TATATTTCTCCTAAA | 8945 |
rs535065033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552055 | TCTTCCTTAGACTTC[C/T]GTGTTACTTTGCCAT | 8945 |
rs535083937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547522 | ATCTTTGTATTTTTA[C/G]TAGAGACTGGGTTTC | 8945 |
rs535113246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377404 | CATTTCTCTAAATAC[C/G]CATGAGGGAGAATTG | 8945 |
rs535127927 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470357 | TTTTTTTTTGAGACG[G/T]AGTCTCGCTGTGTCG | 8945 |
rs535139989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101427335 | GTTGGCCAGGATGGT[C/T]TTGATCTCTTGACCT | 8945 |
rs535143732 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101389773 | GAGACCACAGGTGCA[C/T]GCCACCATGCCTGGC | 8945 |
rs535163129 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101365484 | TTATTTTTATTTTTA[-/T]TTTTTTTTGAGACGA | 8945 |
rs535165176 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101413268 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 8945 |
rs535169474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509497 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 8945 |
rs535173869 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421704 | TTCAATTCCCACCAA[C/G]AGTGAGAACGTGCAG | 8945 |
rs535182905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518534 | CATAATCTCCGCCTT[C/T]TGATGGGAGGAGTAG | 8945 |
rs535189009 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354579 | ACGCCGTGAGGCCGC[A/T]GGCGGGGCCTTCCTG | 8945 |
rs535198622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101450116 | TGGACTATTACTTCT[A/G]ATGTGGAGCATATTA | 8945 |
rs535245400 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101384110 | AGGTATCCATAGTGA[C/T]CAGTTTGTGCTTTCA | 8945 |
rs535248123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101513476 | CAGGCAACCACTGAT[C/T]TGTTTTTCTAACAAT | 8945 |
rs535251196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101462915 | CTCTGTCGCCCAGGC[C/T]GGAGTGCAGTGGCGT | 8945 |
rs535259928 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101357784 | TGACCATAATTCACA[C/T]GTGATCGAGACTTAA | 8945 |
rs535268980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101453950 | AGCCACAGACAAATC[A/G]TAAATGGATGGGCAT | 8945 |
rs535272877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101392557 | GCTAGAGTGCAGTGG[C/T]GGCATGGTCTTGGCT | 8945 |
rs535278344 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400365 | AAGTTAAATTAAGGA[A/G]TACCCAAGAGGGCTG | 8945 |
rs535295754 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532808 | CGTGTGCGCGCGCGC[G/T]CGCTTAGCTATACCT | 8945 |
rs535388280 | snp | C/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352988 | CTCCCACAGTGCTGG[C/G]ATTACAAGCGTCAGT | 8945 |
rs535440187 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556260 | GAGAAAAAAAAATGC[A/G]CTCTTCCCTTGCCGG | 8945 |
rs535443859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407231 | TATACACCTGTAGTC[C/T]CATCTACTTGGAAGG | 8945 |
rs535447902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506773 | CAACTGAAGTTTACT[C/T]ATTTCCTAGCTATAG | 8945 |
rs535459562 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101456498 | TAGAAATGAGTGGAG[-/A]ATGGTAAAAGAGTGC | 8945 |
rs535461342 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504919 | CCCATATTCTTCAAA[C/T]ATTTGACTAATAAAT | 8945 |
rs535461399 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101538496 | CCTACAACTAAGTGG[G/T]AAGGCAACCAGTACA | 8945 |
rs535470500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429875 | TCCTTCTAAAAAAAA[A/G]AAAAACTCTCTTAAC | 8945 |
rs535492571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548639 | CATCTGTAGTCCCAG[A/C]TACTTGGGAGGCTGA | 8945 |
rs535504343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101398538 | TCAATCTCCTGACCT[C/T]GTGATCTGCCTGCCT | 8945 |
rs535528055 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557306 | TACAAATATAAGATT[A/G]AAGTGAATTTTCTAA | 8945 |
rs535534235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488483 | CCATTCAAAGCTCAG[A/G]TATACTAAAATTGTA | 8945 |
rs535540281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540550 | AAGTCAAGTAATGTG[A/G]GTCCTTCAGCTTTGT | 8945 |
rs535556433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508090 | ATGTTAAATGACTAT[A/C]CTGTCCCTTTAACTA | 8945 |
rs535559370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101440304 | TTTTCTTCTAAGGAA[A/G]CACTATTGATGTATG | 8945 |
rs535559998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101430779 | GTAATATTTGCTCTG[A/G]ACCTACATAAAGCCA | 8945 |
rs535563577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101480527 | ATCCTCACATGATAG[A/G]AGAGACTAGCTAGAT | 8945 |
rs535569933 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503445 | CTTGTGTGAATCTGA[A/G]CAAGTTATTTTGATC | 8945 |
rs535578929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449285 | TTTAGCAAAAAGAAA[C/T]AAAAAACCAGGAAAC | 8945 |
rs535597980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101391570 | TCTGATGTATGTTGG[A/G]GAGACTCTTTATAAA | 8945 |
rs535602999 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101478173 | GGGCATGGTGGCAGG[C/T]GCCTGTAAGCCCAGC | 8945 |
rs535631932 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101413470 | AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT | 8945 |
rs535647111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404977 | CACTCCAGCCTGGGT[A/T]ACAGAGCTAGAATCC | 8945 |
rs535656002 | in-del | -/TT | 0.121369 | 0.214369 | intron-variant | BTRC | GRCh38.p7 | 10:101387529 | ATACCTTCATGGGAC[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs535665276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541292 | TGAGACGGAGTCTCG[C/G]TCTTTCACCCAGGCT | 8945 |
rs535682988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101523002 | CGAGGTCAAGAGTTC[A/G]AGACCAGCATGACCA | 8945 |
rs535683277 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101494807 | AATACCTGCTCAAAT[-/TC]TGTCTGGATTGCAGA | 8945 |
rs535685382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481791 | CACCTATATCCTTTC[A/G]TCATCCTCTTAAATA | 8945 |
rs535685402 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446647 | GGACTAAAAAATTAG[G/T]CCAGGAAAGATTGCA | 8945 |
rs535687713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514568 | AGTGATTCTTGTGTC[G/T]CAGCTGCCCTAGTAG | 8945 |
rs535705271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396384 | TTCTGCCACTATGCG[A/G]AAACTTGAATGGGAG | 8945 |
rs535709349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454952 | CCTAGAACTTCATAT[G/T]TGATTTCATAGAAAT | 8945 |
rs535719725 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406557 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTTT | 8945 |
rs535728969 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101355964 | GTGAAAGTTACTACA[C/T]TTAAGTTAGAAAACT | 8945 |
rs535747686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415415 | TCCTGGACTCAAGGG[A/T]TCTGCCCACCTCAGC | 8945 |
rs535764188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367548 | TAACCATTATCTAGA[A/T]CAGGAATAGAACTTT | 8945 |
rs535782033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555415 | CATCACAAAGGAGAT[C/T]GGGGCGACCCCTGCA | 8945 |
rs535786900 | in-del | -/A | 0.00360793 | 0.0423196 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352129 | TTTATTTATTTATTT[-/A]TTTTTTTTGTAACTC | 8945 |
rs535816880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457362 | TGGTGGGATGTCAGG[A/G]GCAGACAATGTCAAT | 8945 |
rs535819264 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352444 | AATTACTTTTATTTT[C/T]ATTTCAATAGTTTTT | 8945 |
rs535830627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519534 | CCTCTTCTGTAACCC[A/G]TTGAAGCAAACTCTG | 8945 |
rs535850740 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431679 | AGATAGGCTGTAAGT[G/T]TCAGAAGGCTTGTGA | 8945 |
rs535852269 | in-del | -/T | 0.495368 | 0.0478996 | intron-variant | BTRC | GRCh38.p7 | 10:101543615 | CCTGTTTTCATGCTC[-/T]TTTTTTTTTTCTTTT | 8945 |
rs535861298 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101438174 | TCTCACGTCTGTAAT[A/C]CCAGCACTTTGGGAG | 8945 |
rs535904390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390914 | AATTTTATACTTTTT[A/G]AGACTTGTAGGGAAT | 8945 |
rs535908399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502333 | CTTACTGTTCTTCCT[C/T]CCCTGAAGTTGGGTG | 8945 |
rs535915781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511358 | GGTGTCACTTCCTTT[A/G]GAGGCATTTCTTGAC | 8945 |
rs535916342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458190 | CTTGGCAATAAAAGG[A/T]AAAGAAATACTAGTA | 8945 |
rs535931021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498529 | TCTATCCTCAGTCCC[A/G]TAAGCTAATGGTGGC | 8945 |
rs535932330 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394009 | GTGTATAATTGAGTC[G/T]GTACCTAGGACTTCC | 8945 |
rs535934342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452191 | TCTGAGGTGTAGAAG[A/C]CCAGTGCACTATGAC | 8945 |
rs535965488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101382273 | CAGGCATGAGCCACC[A/G]CGTCCGGCCCCTAAG | 8945 |
rs535996562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101423222 | CCTGACCCTCTCTGG[A/G]TCTTATTTACCTTAC | 8945 |
rs536033058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535847 | TATGAAGATTTCACA[C/G]TTGGAAGTCCTTTTT | 8945 |
rs536057290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426654 | ATACTACAAAAATAA[C/T]GCAGATTTTTATGTA | 8945 |
rs536062332 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481130 | GTTTTGTTTTGTAGA[G/T]ATGAGGTGTCGCTGT | 8945 |
rs536068243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472477 | ACCCCTTTCCTAACA[C/T]AGGAAACCTGGTTTA | 8945 |
rs536075294 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101526944 | TAAGAGACTTCACTA[A/C]TTTTTTTGTTGTTCT | 8945 |
rs536077720 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539931 | TTCTTTGCCATCTGT[A/G]TATCTCCTTTGGTGA | 8945 |
rs536083946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101369791 | AATACCACAGGGTTC[A/G]TTCGATAATTTCATA | 8945 |
rs536101052 | in-del | -/TAAGTA | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101380679 | TTCCATTTCCTTGTC[-/TAAGTA]TAAGTGATTGAAACC | 8945 |
rs536108894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472858 | CCTAACATCCCCTTT[A/T]TCCTTGGCTCCGTTC | 8945 |
rs536108933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463932 | AGTAAATAGAATTGA[A/G]TCATCCAGGAAGCTT | 8945 |
rs536124756 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101408992 | AGACGGAGGTTGCAG[C/T]GAACCAAGATTGTGC | 8945 |
rs536180198 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454384 | TAGTTTTATGGTTTC[C/T]TGGAGAAGATGACAG | 8945 |
rs536219710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101355381 | ACCCCTTGGAACATA[C/T]TTCTTTAACTTTGTA | 8945 |
rs536227980 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394210 | ATTTTTTATGATAAT[A/G]TATTCTTTCAATTTG | 8945 |
rs536248745 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427911 | CCTTAAGAAAATTTT[A/G]GTATCATTTACTTAA | 8945 |
rs536299345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470379 | GCTGTGTCGCCCAGG[C/T]TGGAGTGCAGTGACA | 8945 |
rs536337824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502714 | TGTACTCACAAAAAG[C/T]AATACCCACCTCCTC | 8945 |
rs536347546 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362531 | CTCCCGAGTAGCTGG[G/T]ATTACAGGCATGCGG | 8945 |
rs536363456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101521188 | CTAAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 8945 |
rs536385246 | in-del | -/CTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101427502 | TCCCTTCCTTCCTTC[-/CTT]CTTCTCTTTCTTCTC | 8945 |
rs536385919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461849 | ATCTGTATGTATACA[A/G]ATCTTCAAGTGAATA | 8945 |
rs536385944 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101398279 | TATTTTATCTAAAAA[-/TG]TGTGTTGAAAATTTC | 8945 |
rs536388272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471079 | CTTGCACCAAATACC[A/G]TAGTGTCTTGATTAT | 8945 |
rs536437964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444978 | GGGGCTCTAGACATT[C/T]GAAAGATATTACACA | 8945 |
rs536439433 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485005 | TTTCTTCTAGATGTG[C/T]GTGCCGTTTAAGAAA | 8945 |
rs536467798 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101484624 | TTAAGATACTGTTCC[A/G]CAAGTAGCATGTCAT | 8945 |
rs536475522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436120 | TATTTTCATCATTCC[A/G]TTGATTTATCCTGGA | 8945 |
rs536483353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427221 | CTTCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8945 |
rs536504844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476293 | GCCATGTGGGATCCT[A/G]GATTAGATGCTGAAC | 8945 |
rs536536446 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101370616 | ATCCTTCCCTCCCTC[C/T]CTCCCTCCCTTTCTC | 8945 |
rs536542379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485548 | AAGCCATTCCAAGGC[A/C]GTTTTATTTTACAAA | 8945 |
rs536564536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437048 | TGTGACAGAAATGCT[G/T]CTCATTCTGTAGCTG | 8945 |
rs536570445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477665 | TTCTTTCTTTTTTAT[C/T]TGGAGACAATGTCTT | 8945 |
rs536577351 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487875 | CTGTGTTTTATGTTA[C/G]TTTTTTTCTTGCTGT | 8945 |
rs536587553 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488653 | CGTGTTAGTCTTTAC[A/G]TATTAGACTTAGTGG | 8945 |
rs536626599 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353958 | ACGGCGTAGCCTCAG[-/T]TTTTTTTCCTGGGGG | 8945 |
rs536639578 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101538607 | TTTAACAGCTGCACA[A/G]CAACTCTACACAACA | 8945 |
rs536664678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473133 | CAGTGACTAAGACCG[A/C]TCTTTTTTTTTTCTT | 8945 |
rs536668453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101482488 | GCAAGCTCCGCCTCC[C/T]GGTTTCACGCCATTT | 8945 |
rs536674069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529994 | CTTCCACACCGTGTT[C/T]GGTGGGTTCTTAACT | 8945 |
rs536674381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372013 | ACTATTTATTGAAAA[A/G]ATTGTTCTTTTTCTA | 8945 |
rs536684752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424587 | AATTTAGGAGATTTT[G/T]TCATTCAGCTTTCGT | 8945 |
rs536687651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420864 | TAAATTTTATTTTTG[A/G]AAAACTCACTGGTAT | 8945 |
rs536704137 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101473946 | TTCTAGAATTTCTAT[G/T]TAGTTTATTTTTGGT | 8945 |
rs536718722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412866 | TGTATTGTCTTTCCC[A/G]ATGTTAAGCCCACAT | 8945 |
rs536738471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101368242 | GGTTTCTCTCTTGGC[A/G]TGTGATTTCTGCACA | 8945 |
rs536741800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364462 | TTACATCAAGGTCAT[A/G]CATAATAACCCAACA | 8945 |
rs536750659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360617 | CTCAGGTGATCCGAC[A/C]GCCTCGGCCTCCCAA | 8945 |
rs536754029 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | BTRC | GRCh38.p7 | 10:101357001 | GGGTGTGGCAGCGTG[C/T]GCCTGTAGTCCCAGC | 8945 |
rs536780539 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540607 | GATTTTTCATGTTAA[C/T]TTTAAAATCAGTTTG | 8945 |
rs536792621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101474543 | TCATGTACGTAGTTT[A/G]GGTGTTAGCCATAGA | 8945 |
rs536816604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101503939 | TTCTTTATTTAAACC[C/T]GACTGTATTTTTCCC | 8945 |
rs536832305 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101552992 | CCCATCAGGCCAGGT[A/C]ACCTTTGACAGAAGC | 8945 |
rs536834465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439226 | TTTTCTGAGATGGAA[A/G]CACAAATTGGATGTG | 8945 |
rs536845152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101369005 | GCTTTGGCGACAGAG[C/T]GAGACTCCATCTTAA | 8945 |
rs536848871 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509873 | GACTGGCTTTTTTTT[C/T]AAAGATGCTTTTGGC | 8945 |
rs536888963 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101387320 | CATTTATTTTTTTTT[G/T]TATTGGGAACATTCA | 8945 |
rs536901959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101378731 | GGTTTCACCATGTTG[G/T]CCAGGCTGGTCTCGA | 8945 |
rs536914803 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519139 | GCTGGAGTGCAATGG[C/T]GTGATCTCTCCTCAC | 8945 |
rs536942659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495584 | ATTGTCTGTATGTGG[C/T]CATAGGTTTGCAAGT | 8945 |
rs536957435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440830 | CTGGAAAAATGGTGT[C/T]GGTAATTCCTGCTTT | 8945 |
rs536962954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379252 | TGGTAGTCTTCTGAA[C/T]ATGGTCCTCTTACCT | 8945 |
rs536963443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549970 | AGTTTTTAATGCCGT[A/G]GAAATCTACCGATGG | 8945 |
rs536964788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101371407 | GTCTTGAACTCCTGA[C/T]CTCAGGTGATCCGCC | 8945 |
rs536982280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481989 | GCAACAGTCTCCAGT[A/G]AGGTACCCATAGCAT | 8945 |
rs537022022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499960 | TGCAATACAGCAGGC[C/T]ATGGACTATAATGCT | 8945 |
rs537025761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392446 | ACGTATCAAAAAAAA[A/T]TTTAAAGATTATTTT | 8945 |
rs537038909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532880 | TGGGGGATCAGACAC[A/G]TAATAGGACCAACAA | 8945 |
rs537054481 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532123 | TACCTTGCAAAAGGA[A/G]GAATATTTTATAAAT | 8945 |
rs537078129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367773 | ATTCAGGTTGTTGTG[G/T]GAGGTGTGGTGTGTT | 8945 |
rs537102423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376182 | AATAAAAAAATTAGC[C/T]GCTCATGGTGGCCCA | 8945 |
rs537107330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101551714 | TCTTTGCAGTGTTCC[A/G]CTGAGGACAGTGATT | 8945 |
rs537147672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492877 | AACTTGAATACATCT[A/G]GCCTGGGACACTAGA | 8945 |
rs537155972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543494 | TAATCCAGCCTGACC[A/G]TCTCTGCCTTTGTCA | 8945 |
rs537168931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525011 | TACGGGAGTGAGAGT[A/G]TGAAGGAATCCTTCT | 8945 |
rs537169461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416543 | GTGTCAATTGAAAGC[C/T]TGAGTTGTTGTTGTT | 8945 |
rs537193045 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101456771 | TCAAAGTTGACAGGG[A/C]GACTTTCATTCTGCC | 8945 |
rs537194218 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101422063 | CTGTCTTCCACAATG[A/G]TTGAACTAGTTTACA | 8945 |
rs537205133 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101525848 | GAAAAATTATTGACA[A/C]TCATTTTACCCAAGC | 8945 |
rs537211752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506980 | AGTTCATACCATGTC[C/T]TAGGAATCCAGAATT | 8945 |
rs537220712 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398094 | TGTGGTAATGGCATT[A/G]GCATCTCTGTATTAG | 8945 |
rs537222706 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353344 | CCATTATATTCCACC[A/G]TTGAAGGACTTTTGT | 8945 |
rs537228510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101466854 | CCATATTCCCCTCCC[C/T]TGAAAAAATTCCTGC | 8945 |
rs537250426 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543350 | TTCTGCTTTTTTATG[A/T]TTAGTGTCTGTGTGG | 8945 |
rs537257747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101498457 | ACCACACCCGGCCTC[C/T]GAAGCTGCTGTTACG | 8945 |
rs537286253 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380145 | AAAACAAGACCTGGT[A/T]TTCAGGTTCTGCTTC | 8945 |
rs537286654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390885 | TTAAGGAGGTGCATC[A/G]GTTAAGATAGATTAA | 8945 |
rs537291773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517988 | CGGGATCTCGGCTCA[C/T]TGCAAGCTCCGCCTC | 8945 |
rs537336539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498952 | GAGCTGAGATCATGC[C/G]ATTGCACTCCAGCCT | 8945 |
rs537337182 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369168 | AGACATAGTCTTTTG[C/T]TGAAGTGTTTATTCA | 8945 |
rs537347773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101449983 | GCATTCGTACATTAA[A/G]CAGGATAAAAATGTA | 8945 |
rs537356935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383305 | CTGGGTTGGGGTCTG[A/C]GAATTTGCATTTCTA | 8945 |
rs537363512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431838 | TTAATATCTTAAGAT[G/T]TTCAGTTTTCCTTTA | 8945 |
rs537418120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504670 | CTGCTTTCCCATTTT[A/C]CCCCTTCCATTTCCC | 8945 |
rs537433334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441842 | GCCGAGATCACACCC[A/G]CTGCACTGCAGCCTG | 8945 |
rs537440715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101488824 | GTACCCACCTGGGTA[C/T]AGAATTGGTAGGAAA | 8945 |
rs537449050 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101495775 | GAATTTTCACGAAGT[A/G]AACATACCTGTGTGA | 8945 |
rs537456378 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517004 | GAAGTGGCATTTAGT[C/T]AAGCTTATAAGCCTG | 8945 |
rs537463687 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101492058 | TTTTCACACAGACTC[A/G]TAAAGTATGTAAGAA | 8945 |
rs537470193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442710 | GTAAAAAGGAATTAA[C/T]GTTTTTGAAATGTCT | 8945 |
rs537499108 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101379405 | CTTTTGAAAGCATTC[A/C/G]TGTTAAAAAGAATTA | 8945 |
rs537502827 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101388950 | TCTTTCCTGTCTACA[C/G]TTTGTTCCTAGATGA | 8945 |
rs537520961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542762 | TATTTTTTTTTAGAG[A/G]TGGGGTTTTGCCACA | 8945 |
rs537538855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486513 | CGTCACATTACCTAG[A/G]AATCTTAGTGTAGAA | 8945 |
rs537553272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101429220 | ACTGTAATAGCACTC[A/G]AGTTGATGGATAAAA | 8945 |
rs537553855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101434462 | TCATAGACCTAAATC[A/G]GAGTTAACATGTATA | 8945 |
rs537556658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547443 | CCTCCTGGGTGCAAG[C/T]TATTCTCCTGTCACA | 8945 |
rs537605829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520464 | CAGTGTTTGGCACAT[A/T]ATAGAGGTTCAGTAA | 8945 |
rs537610158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517199 | TGCTAGAAAACATCC[A/G]CCTCAACACACCAGG | 8945 |
rs537616318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361404 | TGCCACCGCACCTGG[C/T]CAGCAATATTTTAAT | 8945 |
rs537623776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101356374 | TACAGATCATAAAGA[A/G]ACATTATGAGATCAT | 8945 |
rs537623788 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101364331 | AATCTTGACTATTCC[A/G]CAGTGATGCCCTGAA | 8945 |
rs537626012 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101494513 | TTAATTTTGAGAATG[C/T]GGAATATTGAGCAAG | 8945 |
rs537651337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101399558 | TGCCTAGCTGTTGTT[G/T]CCCCACTGGAATGTC | 8945 |
rs537693835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101512508 | TGCAAACTAGAAATA[C/T]TTGTCATTTCACCAT | 8945 |
rs537717267 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101542577 | GACAGCTTTTGCTTC[A/G]TGGTTTTTGTTTGAG | 8945 |
rs537718521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394703 | GGGCAGGGTATAACA[C/T]TCTTGAGAAGAGTGA | 8945 |
rs537734854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356930 | GGTCAGGAGATCGAG[A/T]CCATCCTGGCTAACA | 8945 |
rs537753691 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101366527 | ATTAGTTTTAATGAG[A/C]GATTTTTTAGAAGCT | 8945 |
rs537829370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395246 | GGGGTTTTGTATATT[A/G]TTTCAACCCATTCCG | 8945 |
rs537840018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414500 | ATGTACTTACTGTAC[A/T]GTATTTTTTATTGTT | 8945 |
rs537840736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405579 | GGATACTGGAGGAAT[A/G]ATAAAAAGATAAATT | 8945 |
rs537851574 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364324 | TAATCAGAATCTTGA[C/G]TATTCCACAGTGATG | 8945 |
rs537901117 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555343 | GGGTTTTGCTCTCCA[A/G]TCTAGGTTCAGTTGA | 8945 |
rs537910470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464537 | TTTAACAACCTTCCC[C/T]CCCACCCCCCCCATG | 8945 |
rs537914741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446679 | TATTCAACACCATCA[A/G]AAATGAAGTCTAGGC | 8945 |
rs537920248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407059 | TTTCTTGTAGCCACA[C/T]TGAAAATGTGAAATG | 8945 |
rs537940755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516257 | GAGGGTTTTTTAATT[G/T]GTTCCTTACAAAAAC | 8945 |
rs537941690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101496759 | GAAGTTCTTGTTCAA[C/T]GCATTTGCCCTTTTT | 8945 |
rs537958288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438105 | GGTCTAACTTTTTAC[A/G]TGTGTTGGATTAGAT | 8945 |
rs537978591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487116 | AATATTTGTTGTTAT[A/G]TGGGACAAAATAAAA | 8945 |
rs537978609 | in-del | -/GTT | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101491960 | TTGTGTGTATGTGTA[-/GTT]GTTGTTGTTTTTTTT | 8945 |
rs538001678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457156 | TTACATGAATATGCT[A/C]TCTCAAAATATCTTA | 8945 |
rs538007340 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101529962 | GCAGTTAGTACACCC[A/G]TAGTGGGGTTTACTA | 8945 |
rs538042966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101412773 | CACATGACTATGTGA[A/G]AAACAGATACACACT | 8945 |
rs538064817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101470355 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTGTGT | 8945 |
rs538082620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101540375 | AGCACCATTTATTCA[A/G]AAGACTGTCCTTTCG | 8945 |
rs538087766 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101461778 | TACTTCCCATCTAAA[C/T]CCTTACATAATTTAT | 8945 |
rs538090861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101430677 | GTTACAAAAATTGAC[A/G]TAGTACAGCTTGACT | 8945 |
rs538103703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461802 | AATTTATTTATATAC[A/G]TGGGCATATGTTTTC | 8945 |
rs538146041 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101373790 | AGGCATGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 8945 |
rs538157669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366434 | ACTTTGTTAAGTGCT[A/G]AAATAGTGGCACAAA | 8945 |
rs538169363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422950 | TTGACTTGGCAATGC[A/G]GGCTCTTTTTTGGTT | 8945 |
rs538175020 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101522383 | AAAAAAAAACAAAAA[A/C]AAAAAAACTCTAGAA | 8945 |
rs538175342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413757 | GTTAGATTGTGACCT[C/T]GCTTTGTTTCTAATC | 8945 |
rs538189087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453926 | CCTCTTCCGTTGTAG[C/T]GTGAAAGCAGCCACA | 8945 |
rs538191446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431328 | GTAATCCACCCATCT[C/T]GGCTTCCCAAAGTGC | 8945 |
rs538196396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522931 | TACAGATGGGTTGGG[C/G]ACGGTGGCTCAGGCC | 8945 |
rs538198728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463205 | TGCCCACTACCACAC[C/T]GGGCTAATTTTTGTA | 8945 |
rs538210894 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373735 | ATCCTGGCTAACATG[A/G]TGAAACTCAGTCTTT | 8945 |
rs538215538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526842 | AATGAAATTAAGTAT[A/T]AATCATTGTTTCTTC | 8945 |
rs538215696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407283 | AGCTCAGGAGTTTGA[A/G]GTTCTAGGGAGCTGT | 8945 |
rs538218704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463914 | TTATAAAAATAATTG[G/T]TTAGTAAATAGAATT | 8945 |
rs538235946 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101420967 | TCGCTACAGGTTTAT[A/T]CTCATATTTTCATGC | 8945 |
rs538240033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406406 | CCTGACCTCGTGATC[C/T]GCCCGCCTCAGCCTC | 8945 |
rs538253817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514080 | GATCTTTTTTTGTGA[A/G]GTATCTGTTCAAATC | 8945 |
rs538261606 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101410111 | TTCTTGTTTTAATTG[G/T]AACGTCAAAAGCTTT | 8945 |
rs538265782 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546954 | GAAGAAGTTATATCA[A/G]TTTTCTGTTATCTCT | 8945 |
rs538276310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467490 | GACACTTCTCCCTCT[A/G]GTGGCAATAGTAAGC | 8945 |
rs538296871 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101456068 | CCCAGCTACTCGGGA[A/G/T]GCTGAGGCAGGAGAA | 8945 |
rs538305139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101397208 | AGTATCCTTAAGAAT[A/T]CAATCCTAAAATAAA | 8945 |
rs538312756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459782 | AGTGGTTATCCATCT[A/C]AATCTGATAAAATAG | 8945 |
rs538324233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506414 | TAGCTCATGTTTTTT[G/T]GTAATATTTCAATAT | 8945 |
rs538379573 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352200 | GTTTTCATACGAATG[C/T]GTTTGAAGTCTTCTC | 8945 |
rs538423799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491962 | GTGTGTATGTGTAGT[A/T]GTTGTTGTTTTTTTT | 8945 |
rs538431393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429787 | ATAGCAGACTAACAA[C/G]ATACATAAAACATAC | 8945 |
rs538445123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542712 | GAGTAGCTGGGACCA[C/T]AGGCGTGCGCCACCA | 8945 |
rs538446219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491570 | GGTGTGGTGGCAGGC[A/G]CCTATAAGCCCAGCT | 8945 |
rs538450192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101433551 | AGAGCCAGTGAGGCT[C/T]GGTGCATTTAAGGAC | 8945 |
rs538479486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425604 | CAGGAGAATGCGTAG[A/T]TGCTGCTTAGTTTAA | 8945 |
rs538492558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376083 | GTAATCCTAGCACTT[C/T]GGGAGGCTGAGGCAG | 8945 |
rs538495382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471455 | TAGGATTTTGCCCCC[A/G]TTATTCTGTTAATAC | 8945 |
rs538518998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365506 | TTGAGACGAAGTTTC[A/G]CTCTTGTTGCACAGG | 8945 |
rs538538829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101358172 | TAGAGTGCAGTCATA[A/G]CTTGCTGCAGCCTCA | 8945 |
rs538565734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426458 | ACCGGTATATCTAGT[A/G]GCTTTCCTGGGTGTA | 8945 |
rs538581696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472308 | TCTTCTCTTCTCTTC[C/T]CTTCTCTTCTCTTCT | 8945 |
rs538592524 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | BTRC | GRCh38.p7 | 10:101354078 | AGAGGTAAGAGAGGG[A/C]GGGGGGAAGGAAGAG | 8945 |
rs538619247 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101409170 | CTACTACCTCTATGT[A/C]GTTGAAAGACATTTA | 8945 |
rs538620564 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406325 | GGGACTACAGGCGCC[C/T]GCCACTACGCCCGGC | 8945 |
rs538654138 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485403 | GCCTGAAGTCCAGCC[A/C/G]CATTGATTAGGCACG | 8945 |
rs538679227 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375063 | AACCAGGTGTGTGGA[C/T]GCAGGGGAACTTAGC | 8945 |
rs538685469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518614 | TAGTTACCACCACCG[G/T]AATGACCAGGATGAT | 8945 |
rs538707479 | snp | A/C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101426417 | TCTGTGTGGTGTTTG[A/C/T]AAATTAATGCTATTT | 8945 |
rs538719902 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101510273 | CAGCACTTTAGGAGG[C/T]AGAGGTGGGTGGATC | 8945 |
rs538721875 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101519467 | GGCTGTCAGCTGGGG[G/T]CTCCTTTCAGCAGCT | 8945 |
rs538738406 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373215 | AAAGATCTGTAATTT[A/G]CATTTGAATCTGATT | 8945 |
rs538741604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477481 | AGTATTACCAATGTT[C/T]TGTTTTGTTTTTGGT | 8945 |
rs538745897 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101363183 | AGATTCAGTATTATT[A/T]TTATCCCCATTTCTC | 8945 |
rs538758545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363753 | TTAGATCTTGATGAA[C/T]AGATAGATTTTGACA | 8945 |
rs538780577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528958 | CCCCTGGGACATGAA[C/T]TCTGTAGTTTTCTCT | 8945 |
rs538791456 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369944 | ATATAGATGCCGTCC[C/T]TGACTTACTTAGGCT | 8945 |
rs538795952 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101457904 | CTTACACCCTTTCAC[A/T]TAGATTTACCTAATG | 8945 |
rs538828760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452028 | GGCATTCAGATTAAC[A/G]AGGCAGCAGCAATAA | 8945 |
rs538858221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488568 | CTGAGCCAAATCAGC[G/T]TCTGTTTCCTAGACC | 8945 |
rs538867408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502650 | TAGCATCCTTCTTGG[G/T]GAGAGAAGGGGACTC | 8945 |
rs538885046 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101434549 | TCTTAGCTAAGATAC[-/A]AAAAAATATGAACCA | 8945 |
rs538916613 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101552284 | ACCTCCACCTCCTGG[A/G]CTCAAGTGATTCTCC | 8945 |
rs538927407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483776 | ATTGTAGCTTTAAAT[A/G]GACAGTCATTATTAA | 8945 |
rs538935117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368951 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8945 |
rs538959152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493854 | CTTTGATTGTGTGTA[A/G]TAAAACTGTGGCTTA | 8945 |
rs538963712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460026 | ACATTTCAAAAAACA[C/T]AATTAATTTTGAAAT | 8945 |
rs538967922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475275 | CTGGGCGTGGTGGCT[C/T]ACGCCTGCAATCCCA | 8945 |
rs538977932 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101377528 | AGTTGATCTACATCC[G/T]TGTCAGCATTTGGGA | 8945 |
rs538991530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101494879 | TTCAAATGTGAAATA[A/G]ACATTGTTGTGTGGA | 8945 |
rs538998223 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526271 | CACTGAAAGATTTTT[A/G]GGGAGCCAATGAGAC | 8945 |
rs539005291 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101467301 | AGGGAAAAAGGTTTA[A/C]TGAAGTCCCTGATAT | 8945 |
rs539013603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488582 | CTTCTGTTTCCTAGA[C/T]CTTTTTTGGAAGGCT | 8945 |
rs539030961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498401 | CTCAGGTGATCTGCC[C/T]CCCTTGGCCTCCCAA | 8945 |
rs539033277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536978 | CCATGTAAAAGGGTA[A/G]CCTGTTAACAAAACA | 8945 |
rs539051255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101503794 | CTTTGTATTTTCCTA[A/G]TCCCAGTTTTAGATA | 8945 |
rs539054510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101480644 | CATAGCAAAAGCAGA[A/G]TTTTTGTTTATTTTT | 8945 |
rs539056758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428115 | TACATAATTCTAAGG[A/G]GATATTGATGTAAAT | 8945 |
rs539067831 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450216 | GTCACAAAGCTGACT[G/T]TGTTCAGACAGCTGT | 8945 |
rs539098383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101382120 | CCTGAGTAGCTGTTA[C/T]TACAGGCACCTGCCA | 8945 |
rs539114927 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101401154 | TTAATACAATGAAGT[C/T]TCAGAATAGCCAAGT | 8945 |
rs539120490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101371348 | CATGCCAGCTAATTT[C/T]TGTATTTTTAGTAGA | 8945 |
rs539129955 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438592 | ATTTAAAAGAAAGTA[C/T]ATAATTAGTTTTACC | 8945 |
rs539144102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481883 | TTTATTGGCCCACAT[C/G]CTGTCTTCTGGTTCA | 8945 |
rs539144324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101366805 | TTTTACATTTATATA[C/T]ATATTTATATATATT | 8945 |
rs539156295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101419713 | GCATGCATACCAAGC[A/G]GTGGGAAACATCGGG | 8945 |
rs539193783 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434996 | TACTGGTTTTACCCT[A/G]TCAATTCAATAATTT | 8945 |
rs539197605 | in-del | -/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553481 | TATATTTAGTGTTTT[-/G]CCAGAATCTCTCTTG | 8945 |
rs539202677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402167 | GTACACAGCTACTTC[A/C]TATCTGATAAATCTA | 8945 |
rs539211839 | snp | A/G/T | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101505785 | TAAATGCTATTTTTA[A/G/T]AAAATGAATTAAACA | 8945 |
rs539227335 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101467575 | GGGACTGTCTTGTAA[A/G]TACTTTCGTTTGGGG | 8945 |
rs539239322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446848 | TTCTTCCCTCTATCC[C/T]CCAAAGATCTAAACC | 8945 |
rs539241193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406262 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 8945 |
rs539258832 | in-del | -/TAATT | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101396967 | GCCACCTCGCCTGGC[-/TAATT]TTTGGTATTTTTAGT | 8945 |
rs539280332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385348 | CTCCAGCCTAGGTGA[C/G]AGAACGAGACTCTGT | 8945 |
rs539292455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386351 | CCTTAAACATTGTCA[A/G]CATGTTCACTTATTT | 8945 |
rs539334797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101553133 | AAAGGGGCTAATGAC[C/T]ATTTGCTCTGTTTTC | 8945 |
rs539350515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544645 | TCCTGGCCTCACATA[A/T]TCCTCTTGCCTCACA | 8945 |
rs539401890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508383 | CCCTTCCTGTCTTCC[A/G]TGTTCACTAATCAGA | 8945 |
rs539416521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101549308 | TGGTGGCATGAGTCT[A/G]TAGTCCTCACTACTT | 8945 |
rs539435138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101430982 | TTCTAGGTGGAAAAA[A/C]CTTTGAGACCTTTAG | 8945 |
rs539446469 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533216 | ATTTCTGTCAGTCTA[A/G]AACTAGAAAACTTGA | 8945 |
rs539473139 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101423299 | ATTCATTGCCAAACA[A/G]TGAATTGTTAGACTG | 8945 |
rs539505699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392353 | TGAGGGAAGAAACCA[C/T]TGGCAACCCCTTTGT | 8945 |
rs539528373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499841 | TCAAATGGAAATCAA[A/G]CCTCAGTGCTTGTCC | 8945 |
rs539543821 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101532807 | GCGTGTGCGCGCGCG[C/T]GCGCTTAGCTATACC | 8945 |
rs539553917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473082 | CCTTGGACTCCAGCC[A/T]CGCATATATTCTAGA | 8945 |
rs539559202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424002 | TGGGAGGCCAAGGCA[C/G]GTGGATCACCTGAGT | 8945 |
rs539567662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384181 | GTTAAGTCTGTGCAA[C/T]TAGTAAAGCAAGTGG | 8945 |
rs539581596 | in-del | -/AGT | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101386508 | TAATTTTAGATCAGC[-/AGT]AGTACACTTTGGCCA | 8945 |
rs539592535 | in-del | -/TCTCTTCTCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101472275 | TTTCTTTTCTTTTCC[-/TCTCTTCTCT]TCTCTTCTCTTCTCT | 8945 |
rs539617377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359572 | AGCTGGAATTACAGG[C/T]GTGTACCACCTTGCC | 8945 |
rs539628054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396469 | CAGGCTGGTCTCGAG[C/T]GAGGTAAAGATTTTA | 8945 |
rs539633825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533525 | TTTAATTGCAAGCTT[C/T]ACTCAGGTAGGGGCC | 8945 |
rs539665278 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101474850 | CCGTCTTTTTTAAGT[C/T]GATCTCCAGTGCCTT | 8945 |
rs539691649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516516 | CTCATCAAAAAAATA[C/G]TCGTTTTGAGGGGTG | 8945 |
rs539695772 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101366851 | ATATTTATGTATATT[-/AA]TATATATTTATATAT | 8945 |
rs539701530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389862 | CCTCTTGGGTTCAAG[C/G]GATCTGTCTACCTCA | 8945 |
rs539728331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101360478 | TCCCAGGTTCAGGCA[A/G]TTCTCCTGTCTCAGC | 8945 |
rs539728947 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101438964 | GAGATTATAAAACTG[A/C]ATCATGATTTTGGTG | 8945 |
rs539745146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381339 | GGCACAGCTGGTATT[C/G]CAGCTCAGACATTCT | 8945 |
rs539757982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548783 | GGCATGGCTGGGCAC[A/G]GTAGCTAAGGCCTGT | 8945 |
rs539821199 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502493 | TTATTAAGTTTCATG[A/G]AACATTAACCTACTG | 8945 |
rs539828308 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101539749 | TTTTTAGAAACTGCC[A/G]AACTGTTTTTCAAAG | 8945 |
rs539830375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449397 | TTTGATAAAAAAACT[A/G]CTTAAGAAAATCTAC | 8945 |
rs539831542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552608 | GTCTCCAGTCCAAGC[C/G]TCTGCCTTAATCTCC | 8945 |
rs539840830 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460667 | CAGAATGACACAGTA[C/T]GTTTTTTATCTCTCA | 8945 |
rs539912754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435289 | CAAATGCATACTTTT[A/G]TGTAACCTTCAATTT | 8945 |
rs539920880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490973 | TGAGGTGGGGAGACT[C/T]ACTTGAACCTGGGAG | 8945 |
rs539945966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375554 | GGCAGGGAGTCTGGG[A/G]CAGATATTCTGGGGA | 8945 |
rs540017521 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101415559 | ATGTTATGTTATTTT[A/G]AGACAGAGTTTCACT | 8945 |
rs540027517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101518793 | GCTGTCTAGTCCTCA[A/T]TTCCTTCATGTCTGA | 8945 |
rs540044773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416474 | CTTTGGTTCAGTTGA[A/G]GCATCTCTGTTTTTG | 8945 |
rs540045013 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101401850 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 8945 |
rs540084827 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101410562 | GAGATTGCAGTGAGC[C/T]GAGATCATGCCACTG | 8945 |
rs540096118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457473 | AGAAAGGTGCACAAT[A/T]GAAAACTATTTCTAA | 8945 |
rs540104243 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352648 | CCTATAAGTCAAAAA[A/G]TATTTTCCTAGTTCA | 8945 |
rs540115390 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101451656 | ATTTTTTCCCCCCTG[A/G]GGTCCCCACACACCT | 8945 |
rs540121730 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415995 | ACCTATAGTCTAGGC[A/G]TGTGGTAGTACCTTC | 8945 |
rs540180312 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101512239 | CAAAACCCTTGCCTA[C/T]TTTATTCTTAAATTA | 8945 |
rs540180506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446338 | GGTTGTCTTTGGTTA[C/T]TTGTCTCTTGCCTTT | 8945 |
rs540207553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443256 | AACCCTCCTAAGTGA[A/G]GTCAGTTATTTTGTT | 8945 |
rs540254391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101462140 | CTTGATTTGCCATTC[A/T]TTAAGCACTGGAGCT | 8945 |
rs540256103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453558 | ACTCAAAGATTATTG[G/T]AAGTCATTATGAGTG | 8945 |
rs540267140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386650 | AGCACATGAAGAACC[A/G]AGGACTTGTTTGACT | 8945 |
rs540272494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494217 | AAACTAAGGTGGTAA[A/G]TTGGCATCTTGGCTT | 8945 |
rs540282087 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101495701 | GCTAGGACAGTCTAT[-/C]TATAGCCAAACAGAA | 8945 |
rs540283541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377826 | AGCCTATCTACAAAG[A/T]TTTAAGTAAGCCATG | 8945 |
rs540292025 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101387609 | TTGGCTCACTGCAAC[C/G]TCTGCCTCCTGGGTT | 8945 |
rs540298450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504355 | AGAGCAGGTGAGCTT[A/G]GTAATGCTGGGTCCC | 8945 |
rs540307053 | in-del | -/TACCTCAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101524300 | AAAACAGTCTGTGTG[-/TACCTCAT]TACCTCATTACTTTG | 8945 |
rs540339770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387749 | GGCTGAAGTGCGGTG[A/G]CGCGATCTCTGCTTA | 8945 |
rs540353407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370919 | ACACACAGACACACA[G/T]ACATATGTACCTATA | 8945 |
rs540398369 | in-del | -/TCTCAT | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101388517 | TTGATTGAGACAGGG[-/TCTCAT]TCTGTTGCCCAGGCT | 8945 |
rs540416424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410303 | TTGATTTTCATTTTC[C/G]CAATGACCGCTGATG | 8945 |
rs540421443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101428433 | TCGTAGCTTGAGGTG[A/G]GGAAACGTTGAAAAC | 8945 |
rs540443426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101477022 | TGCTCTGTCACCCAC[A/G]CTGGAGTGCCGTGGC | 8945 |
rs540449831 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402639 | GTGGAATTTTATTGC[G/T]GTAAGGTAGTTAGAA | 8945 |
rs540457927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460096 | GATCTTTTTATTTAT[G/T]TATTTAAAGGAGGAA | 8945 |
rs540461552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437242 | TGTTTGTGCAGAAAT[A/G]TTTTGTTCTCCTAAT | 8945 |
rs540488377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411593 | TTTCATGAAATTATC[A/G]TTTCAAACATTGTAT | 8945 |
rs540534687 | in-del | -/TTGTT | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554422 | TTTTTGTTTTTTTTG[-/TTGTT]TTGTTTTGTTTTGGC | 8945 |
rs540538748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101511501 | CAAGTAGCTGGAACC[A/G]CATGTGCGCACCACC | 8945 |
rs540560859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461431 | TTTTAGGGCCTCTAG[C/G]TGCTGTTTGAGGTGA | 8945 |
rs540623006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512706 | TTTTGAAAGTGGTAC[A/G]TGAAATATGTTTTCG | 8945 |
rs540627031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101403675 | GGCTCACTGCAGCCT[C/T]GACCTCTCAGGCTCA | 8945 |
rs540649546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457919 | ATAGATTTACCTAAT[A/G]TTAACATGTTACCAT | 8945 |
rs540659485 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101513792 | AAGGAGGTAAGTACC[G/T]AAAGTGGAATTGCTG | 8945 |
rs540683816 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101404997 | GCTAGAATCCATCTT[-/A]AAAAAAAAAAAAAAA | 8945 |
rs540686339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458299 | TTCCATTTATATGAC[A/G]TTCTGAAAATGGCAC | 8945 |
rs540695682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517351 | AATAAGCAAGCCTCA[A/G]GAGTTCAGGGCTGCA | 8945 |
rs540695970 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499188 | TGTTCAGGTCTATAT[A/G]GCTTGTACATGGCAG | 8945 |
rs540702224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395652 | TGCTATGAAAGATCT[G/T]AGATTTATTTTTGGT | 8945 |
rs540741921 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530837 | AGAGTATATGGAATG[A/G]TAACCGTGAAAACAC | 8945 |
rs540757021 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554476 | AAATATTGATCTCAC[C/T]GTGTCAACCTTGCAC | 8945 |
rs540786751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508642 | AAAGTAGGCTGGGCG[A/T]GGTGGCTCACGCCTG | 8945 |
rs540795920 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101485642 | TGAACCGTTTTTTTT[G/T]TTTTTGTTTTTGTTT | 8945 |
rs540817900 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | BTRC | GRCh38.p7 | 10:101432135 | ATATCTTTTTTTTCC[C/T]TTTTTTTTTTTTGAG | 8945 |
rs540828354 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101528588 | ATAAACCCATGAAAT[G/T]CCAAATACTTATACA | 8945 |
rs540830998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101477759 | GGCTCAAGCGATTCT[C/T]GTCCCTCAGCCTCCT | 8945 |
rs540834498 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468709 | ATATCTTGTTATGCT[A/G]TAGGGCTGCTGAACA | 8945 |
rs540845825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541444 | TTTTGTATTTTTTAG[G/T]AGAGACGGGGTTTCA | 8945 |
rs540857692 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101529241 | GTTTTCAGTACCTAG[C/G]CACCTCTTTCTGTAA | 8945 |
rs540865245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363382 | TATCTGTTAAGGCAC[A/G]CTTTGGTAAATGCTA | 8945 |
rs540865318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371590 | GTCCTCAGGTTTCAT[C/G]CATGTTCTTCCTTTT | 8945 |
rs540897224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424183 | AGGTTGCAGTGAGCC[A/G]AGATCATGGCATTGC | 8945 |
rs540917041 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101469839 | TTCTAGAATTTTGTG[C/T]AATGGAATGCTATAT | 8945 |
rs540953615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412157 | GGAATTTCACTGTAT[A/G]TATACAGGACTTAGT | 8945 |
rs540960963 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475321 | AAGGCAGGTGGATCA[A/G]TTAAGGTCAGGAGTT | 8945 |
rs540966448 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101473283 | TTTTAAGCCTCTCCA[A/G]TAAATTTTTTGATTT | 8945 |
rs541006986 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101354020 | TGGGCTTTCGCCTGC[C/G]CACGGAGAAGCCGAT | 8945 |
rs541022199 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101373036 | GTTTGAATTTCTCTG[C/T]TTAGAGGTCTTTATA | 8945 |
rs541030657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101444257 | TAAAAAGAGATGATA[A/G]TATTTGTTACAATGC | 8945 |
rs541031970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483402 | GTTCAAGACCAGCCC[A/C]ACCAACATGGTGAAA | 8945 |
rs541034887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399044 | TGCAACGTCCGCCTC[C/T]TGGGCTCAAGCGATT | 8945 |
rs541036804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101408301 | TCTTTTTCTTCTTTT[C/T]TTTTAAATTTATTTT | 8945 |
rs541039804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428727 | TAAAATGAGGATAAT[A/G]TATTAAGCGTAGTCC | 8945 |
rs541052063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507444 | GCTCTGTGCCGCTCC[A/G]ATCCGGGGAAATGAT | 8945 |
rs541074725 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377055 | ATTGTATCACTCCCC[C/T]GCAAAAAACTCTTAT | 8945 |
rs541076784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474836 | TCCTTCCCCATTTTC[C/T]GTCTTTTTTAAGTCG | 8945 |
rs541091828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526503 | GTATCCTGTGGCTGG[A/G]CACAGTGCGTTCACG | 8945 |
rs541101176 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353490 | CTGACTTGCTGTGGG[A/G]GAGAAAAGATTCCTC | 8945 |
rs541130399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527191 | CTTGGATCATAAAGA[A/G]GAAAACAGTTAAAAG | 8945 |
rs541151928 | in-del | -/CC | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101369259 | TTCTTGCCCTCTTGT[-/CC]AGGCTCTCGAGTACA | 8945 |
rs541170838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354288 | TGGCGGCGTCGCTGG[C/T]CTGGGCCGCCCGCCC | 8945 |
rs541181836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499316 | ATCTGGGCTCACTGC[A/T]ACCTCCGCCTTCTGG | 8945 |
rs541192580 | in-del | -/ACACAT | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101438500 | ATGTTTTTATGTCTC[-/ACACAT]ACACATACATATATA | 8945 |
rs541193146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481186 | TGGCCTCGAGTAATC[C/T]TCCCCACTAGGCCTG | 8945 |
rs541198009 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101386254 | GTATAACCAAGCAAA[-/TG]CCCAGCAAGGTCAGT | 8945 |
rs541199994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409588 | TGTTATAGCTTGTTG[C/G]TCCCAGGCTACCTGG | 8945 |
rs541206447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532517 | AGCATAAACTCTAAG[C/T]ATTATTTCTAGAAAG | 8945 |
rs541218424 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505276 | CCCAAAGTGCTGGGA[G/T]TACAGGCATGAGCCA | 8945 |
rs541241066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101415087 | ACCTTCACGTTTATT[A/G]ACCACTCATTCAGTA | 8945 |
rs541249907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101441378 | CCAGGCTTGCCTCAT[A/G]AGCAAACATCAGTGT | 8945 |
rs541252310 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101541703 | ATCATATGGTTTTTC[A/G]CTTTTATTCTGTTAA | 8945 |
rs541261835 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101367150 | ATCTTGGCTCACTGC[A/T]TCGTCTGCCTCCCAG | 8945 |
rs541265520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500228 | CTAGGCTATATGGTA[C/T]ACCTATTACTCCTAG | 8945 |
rs541265594 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101550338 | TGCCCAGGCTGGAGT[A/G]CAGTGGAGTGATCTC | 8945 |
rs541267416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491341 | AGCATGCACTGGCAG[C/T]CCTTTCATACCAACA | 8945 |
rs541302819 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101492120 | GACAAACAGGAACAG[C/G]AAAATATTTCTAGAA | 8945 |
rs541312675 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101359260 | CAGTGAAATTGATTA[A/C]CAGGTAGTGGGATGA | 8945 |
rs541330195 | in-del | -/GATAGATT | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101436668 | ATAGATAGATAGATA[-/GATAGATT]GATTTATATGGCCCT | 8945 |
rs541336099 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101509032 | ATTCTTTCAGTTTAT[A/C]TTGAAATCTCCTTGT | 8945 |
rs541346358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368669 | CATTTTATACTTTCT[G/T]TAGCAGTGTATGGGA | 8945 |
rs541373821 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101537827 | TGGCTTTGATCTGTA[C/T]CCACCTGTCTTGGAA | 8945 |
rs541428667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425980 | TATTTATTAAATGTT[A/G]AAGGACAGAAAACAT | 8945 |
rs541439008 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406042 | TCTCAAACTATGTAG[A/G]TTTGTGTATTTTCCC | 8945 |
rs541457596 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101372247 | GCCTTTTGCGTTTTC[G/T]TTTTCTTTTTCTTTT | 8945 |
rs541523556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362429 | AGATGGAGTTTCGCT[C/T]TTGTTGCCCAGGTTG | 8945 |
rs541529299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531420 | TTACAGCAAGCCCAT[A/T]AAGGTTTATTGACAT | 8945 |
rs541531350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418273 | CTCAGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA | 8945 |
rs541548536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479676 | TCTGGTCACTCTTTA[C/G]ACTGATTCACATTTG | 8945 |
rs541573497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101467706 | TTGGGTAAAAAAAAA[A/G]TTGCCTGAGATGTTT | 8945 |
rs541575299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422271 | GCATAAATGTCTTCT[C/T]CTGAGAAGTGTCTGT | 8945 |
rs541577235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365602 | TGCCTCAGCTTCCTG[A/G]GTAGCTGGGACTACA | 8945 |
rs541595974 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358260 | ACCACTATGCTGGCT[A/G]TTTTTTTTTTCTTTT | 8945 |
rs541604997 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101530137 | ATAAGGAAGGAGATA[A/C]TAACAAATGTTGCTC | 8945 |
rs541626576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550515 | TCTCGATCTCCTGAC[C/G]TCGTGATCCGCATGC | 8945 |
rs541660446 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101528947 | TTGACAGTCTTCCCC[-/T]GGGACATGAACTCTG | 8945 |
rs541661968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504852 | CTTGCTCTGATCAAT[C/T]TGATATTATGAACAA | 8945 |
rs541664234 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527708 | GCAGTGAGCTGTGGT[C/T]ATGCCACTGCACTCC | 8945 |
rs541666780 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101384345 | CTAAATCACAGCCTT[A/G]AAGCAGCTATTTCTT | 8945 |
rs541686089 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101544164 | TCCGCCCGCCTCAGG[C/T]TCCCAAAGTGCTGGG | 8945 |
rs541689923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482853 | TGCAGTGTTTTCTCA[A/G]CTTGGTACAAGTGTC | 8945 |
rs541697721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495887 | TGAAAAGACCATTAC[C/T]GGAGCCCACTACTAC | 8945 |
rs541711430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546016 | AAATAGATGCATCCA[C/T]TGTTATAGTTGGAGA | 8945 |
rs541713116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101433007 | GTATGGTTTAGTGCC[C/T]CCAACATGAATCACA | 8945 |
rs541717825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388110 | AACCAAAGTATGGAG[C/T]TACTTCAAAATTAAA | 8945 |
rs541721076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551263 | CAATACCTACAATAG[A/G]GACCTTTCAAGCCAA | 8945 |
rs541726078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445976 | GAATAGGAATGATAA[C/T]GTGGCACTGGGACGG | 8945 |
rs541759628 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375151 | TCCCCAGTGTTGGAG[G/T]TGGGGCCTGGTAGGA | 8945 |
rs541762465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428741 | TGTATTAAGCGTAGT[C/G]CTATGGGTGGTAAAT | 8945 |
rs541772016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101486579 | TAAAGAGGGGAGGTG[A/G]GGAAAAGAGTGTGTG | 8945 |
rs541786255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539229 | GGAATGCACTAAATT[A/G]TTTATCATGTTGTTA | 8945 |
rs541808340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101397803 | GCAATTGGTAAGGCA[A/T]CACATGCAGCATTAT | 8945 |
rs541832861 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556647 | GGAATAAAACAGTTT[C/T]GCTTCTTTAGCTCAT | 8945 |
rs541836132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469414 | TCTGGAAACTCCCTC[A/C]GGCCTGGCACAGAGT | 8945 |
rs541838155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447889 | TTGTTTATCACTTTT[C/T]TTCTTTAATCAACCA | 8945 |
rs541839085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421421 | CATCTTTGTTGCTTA[A/C]TAACTACTCATCAAC | 8945 |
rs541846366 | in-del | -/GAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101440374 | TAAAGTTTTAACTGA[-/GAAT]GAATGGCCTTTTGCA | 8945 |
rs541858795 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472149 | TGAAACCATTAGTTC[A/G]CATTGATAACTCCAA | 8945 |
rs541904497 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101364885 | CTGCAATACCAGGTC[A/G]ATGCATGGAGTGGAC | 8945 |
rs541915044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101357495 | CATCAAATAATTAGT[A/G]CACAGTACACATGGA | 8945 |
rs541926635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101431224 | TGGGATTACAGTTAC[A/G]CGCCACCACGCCTGG | 8945 |
rs541941768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413180 | CCCAGGCTAGAGTGC[A/G]GTGGTGCAATCTCGG | 8945 |
rs541982673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101462257 | TCTAGGTATACATGT[A/T]CAGGACAGCTGGTTG | 8945 |
rs541988331 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101445283 | AATATGTCCCTTTTC[A/G]TTCCTGCATCTTACT | 8945 |
rs541993664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549486 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 8945 |
rs542029005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405751 | TTACTCCATCTTACA[C/T]GGAACTAGAACCCCT | 8945 |
rs542092168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396615 | TACTTAGGACAGGTA[C/T]TAATGGACACTTTCT | 8945 |
rs542113722 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101436668 | GATAGATAGATAGAT[A/T]GATTTATATGGCCCT | 8945 |
rs542150569 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101437656 | TGGTAATACTGATTT[G/T]GGTCACTGTTTATCT | 8945 |
rs542186290 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101492653 | TGATAGATTGAAGGC[A/G]TTTTCTTTAACCCTT | 8945 |
rs542191555 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101478300 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 8945 |
rs542193173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101389301 | ATACATCTCAAATTC[A/G]TCTACCCCTCTCTGC | 8945 |
rs542196905 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475169 | ATGCTCTATTTTTTC[A/G]TATATATTTTGAAAT | 8945 |
rs542206932 | snp | G/T | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354586 | GAGGCCGCTGGCGGG[G/T]CCTTCCTGGTGTCAG | 8945 |
rs542245298 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440185 | TGGAAAATATTTTGT[A/G]GTAATAAAATGAGTT | 8945 |
rs542253364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381057 | GCATATCTGACCATA[C/T]TTGACTGAAGTGTCA | 8945 |
rs542283675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548985 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 8945 |
rs542284700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498053 | AAGTTGAGATATATA[G/T]TGACATATACAGAGA | 8945 |
rs542319842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488955 | TCATAATAGGTATAA[C/T]TCTCTAGGCTTTCAG | 8945 |
rs542343811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493322 | AGGTATTTATTGAAT[C/G]TTTATGATGTACTAG | 8945 |
rs542363695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538818 | TTTGGGAGGTCAAGG[C/T]AGATGGATCACCTGA | 8945 |
rs542364924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417332 | TCCTTGGCTTTCATA[A/C]CATTGACATTTTTGA | 8945 |
rs542398950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543996 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 8945 |
rs542449919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526352 | CAGAGAACAAATGTT[C/G]ATATACTCAGCAGTT | 8945 |
rs542454659 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101414904 | AAAAGAGTCAAAAAG[-/TTT]TTAAAAACTAAAAAA | 8945 |
rs542462298 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101447545 | CTGTAAGAACAACTA[C/T]TATGATATTAAAATT | 8945 |
rs542495072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101363492 | GAGATGGAGTCTTAC[C/T]CTGTCACCCAGGCTG | 8945 |
rs542508989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101459080 | GCTGGGATTACACGC[A/G]TATGCCAAAGTACTA | 8945 |
rs542569604 | snp | A/G | | | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101515868 | GGTACTACAAATTGT[A/G]TAGGTGGATGGTTTT | 8945 |
rs542569994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510291 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 8945 |
rs542573509 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361629 | CAGTTTCAACTAGTG[C/T]TCCACAATATTTCTG | 8945 |
rs542588963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451608 | ATTCTGGCTTGTGAG[C/G]TAATGACAAGTGTTT | 8945 |
rs542593543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450468 | ATCTCTTCTATCCTT[C/T]TTATCAGAGTATCTC | 8945 |
rs542596297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500343 | AACATAGAAAAGGTA[C/T]AGTAAGAATACAATA | 8945 |
rs542609602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393563 | GTCCTGTCAAAGTAC[A/G]TCACAAAAATCCAGT | 8945 |
rs542627221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469579 | ATTGATGACTGGACA[A/G]ACCTCTGTAAAAAAT | 8945 |
rs542637395 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101463173 | GCCTCAGCCTCCTGC[C/G]TAACTGGGACTACAG | 8945 |
rs542641773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355710 | GATAAACATGGATAC[C/T]AACAAAATTGAATTT | 8945 |
rs542646170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492351 | TATGGAGTCTGTAGC[A/G]TGACTCTGTAATGGA | 8945 |
rs542681645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511839 | CTGTATTAATAGAGA[C/T]GAAGTTTCACTATGT | 8945 |
rs542691121 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524757 | AACTAATTATTATAT[C/G]TTTAATTGGCTTTTG | 8945 |
rs542692102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384497 | TTCTTATGAGTAGTT[C/T]ATGGTAAATTATAGT | 8945 |
rs542712754 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101479091 | CTTCCAATTTGCATT[G/T]TAAAATGCTACATAA | 8945 |
rs542740227 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101552345 | CAACACCATGACCAG[C/T]TAATTGTTTGTATTT | 8945 |
rs542746937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356456 | TCTCTGCTTTGTACC[A/G]GTGAGTTATGTTTTG | 8945 |
rs542761966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101363836 | GTCCAGATTTACATA[C/T]AGGTTTCCTGATTAT | 8945 |
rs542783331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101383542 | TTCTTTCCTTCTTTC[C/T]AGGCTGGAGTGCAGT | 8945 |
rs542788849 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517302 | GTATCTTTACTTTGT[A/G]AAGAGCCCTGTGTAT | 8945 |
rs542792820 | in-del | -/A | 0.418491 | 0.184691 | intron-variant | BTRC | GRCh38.p7 | 10:101486444 | GCACATTTCTCAGGG[-/A]AAAAAAAAAAAGTGG | 8945 |
rs542795625 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101450251 | TATCGCTCCTATTCA[C/G]AAAACAGATAACTGT | 8945 |
rs542828435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484222 | AAAAATGTGATGTTC[A/C]TTTCCACTCACTCCA | 8945 |
rs542842820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101427064 | TACCCAGCACACACA[C/G]AAACTTAACCAATTG | 8945 |
rs542843686 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482581 | TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC | 8945 |
rs542852369 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514903 | CTTGAAATTTACTAG[A/T]CTGAGTCTTCCATCT | 8945 |
rs542857852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467179 | TCTTTTTTCAAGAGA[C/G]CTCCTTTTCTTCCTT | 8945 |
rs542861241 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101371780 | TGCATTTAGCTCTGC[A/G]ATCCATCTGGAATTA | 8945 |
rs542876317 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353670 | AAACCACAGTTAGGC[A/G]GGTCCTAGGACCCGT | 8945 |
rs542879760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418595 | TGGCAATAGTTTAGA[C/T]CTCTTCTAGAATTTT | 8945 |
rs542890024 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549707 | CGAAAGAGCGAGACT[C/G]TGTCTCAAAAAAAAA | 8945 |
rs542894011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370279 | GGTGCTTGCCACCAC[A/G]CCTGGCTAATTTTTT | 8945 |
rs542939587 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354122 | GGCGCTGCGTTGGCT[A/G]CGGCCTGGCACCAAA | 8945 |
rs542939794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469042 | AGCAAGGCATCTTAC[C/T]AGTTTATGCTTATGT | 8945 |
rs542950832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459839 | TATGGGCTAGTCAAT[A/C]CTCAGGCTGTTAAGG | 8945 |
rs542957985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509658 | CCCAGGCTCAAGTAA[C/T]CCTCCCACCTCAGCC | 8945 |
rs542980488 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427871 | ATTTAATAAGTATTT[A/T]TTGAATAAATGATTA | 8945 |
rs543033686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529190 | AAGATCTTCCATCAT[A/G]AAAGGTTTTGACTTA | 8945 |
rs543061066 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547498 | GGTGCCTGCCACCAC[A/G]CTCAGCTGATCTTTG | 8945 |
rs543084279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101524166 | ACCTATTTATATCTT[A/G]GGAATAACCACTATA | 8945 |
rs543118675 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101403652 | CCAGAGTGCAGTAGC[A/G]TGATCATGGCTCACT | 8945 |
rs543122361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512649 | CAAGTGTCTATTTTT[C/G]CCTCCTGGCCCAGGC | 8945 |
rs543146861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453492 | TATAACAGATGTCTC[C/T]TCAAACAGGTTCAGG | 8945 |
rs543173951 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101516648 | CTTATGACTTGATCA[C/T]TGAAAGTATCACAAA | 8945 |
rs543205052 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366564 | AAGAAAGTTTTGTAT[C/T]GGACCTTGAAGAGTA | 8945 |
rs543210073 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445231 | TTTTAGGACATTGGA[A/G]TAGCTGATTGTATAT | 8945 |
rs543217630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484976 | TTTGTCAGATTAAGG[A/T]TGTAAGAATACATTT | 8945 |
rs543218555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494100 | GAGGCTATCAGCAGG[G/T]TAATGAATAACTGTT | 8945 |
rs543233652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427569 | GTCTTGCTTTGTTGC[C/T]CAGGCTGGTGTGCAG | 8945 |
rs543245662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548820 | AACACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 8945 |
rs543258584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370856 | GGATGCTGGGGTTAC[A/C]GGTGTGCACCACTTC | 8945 |
rs543261758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488767 | TGATACTAATAATTA[A/G]GCATTTATTTGAAGT | 8945 |
rs543293826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476948 | AAAATGCAAATGTTC[A/C]GAAGCTCTGGGGATG | 8945 |
rs543302956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101374132 | AGATCCCGGAGGAAT[C/T]GCCACACTGACTTCC | 8945 |
rs543303450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481101 | TAATTTTTGGTTTTC[C/G]GTTTTTTAGAGTTGT | 8945 |
rs543310649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527491 | GGTGGGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 8945 |
rs543325441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431151 | GCGTGATCTCAGCTC[A/G]CTGCATCCTGCGCCT | 8945 |
rs543342035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472644 | ATATGGTGAAACCCT[A/G]TCTCTACTAAAAATA | 8945 |
rs543348507 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101447063 | GTGCAGGTTGGACTT[C/T]TTGCGGGTCAAGGCA | 8945 |
rs543349415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528393 | AAAAAACAATCATTG[A/G]GAAGATGGCTTTTGA | 8945 |
rs543366185 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | BTRC | GRCh38.p7 | 10:101367078 | TAAATATATATATAT[A/T]TATTTTTTTCGAGCT | 8945 |
rs543372760 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419441 | TTGAAGGTTTTATTT[C/T]GAGAAAAAGCCACTT | 8945 |
rs543391080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375185 | GTTTGGATCATGGGG[A/G]CGGATTTCCGCCTTT | 8945 |
rs543391398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101542170 | CCAAGCAGTTTGGCC[A/G]TTTTATCTAAATTAT | 8945 |
rs543423007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464145 | CAATGACACAACAAA[A/C]GTTTTGGCAACTTTA | 8945 |
rs543425355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101491159 | ATACAGATCTTTCAA[A/G]GATCTAAGTTGACTT | 8945 |
rs543426406 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536419 | GAAAGCAGTACATAT[C/T]TGTGTGGGTGGTGAT | 8945 |
rs543443627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432878 | CACAGAGTATTACCA[A/T]CCATGAAATTGACCT | 8945 |
rs543455298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415603 | CTGGAGTGCAATGGC[C/G]TGATCTCGGCTCACT | 8945 |
rs543456902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406858 | TTATGACTGTTTTTA[C/T]GATACAGCTTCTTTA | 8945 |
rs543462499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482684 | ACAGTCGTGAGCTGC[C/T]GCATCCGGCCAACTG | 8945 |
rs543515495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535181 | ATGTGGTAACAGCCA[A/T]CTGCAAATTAGCCTC | 8945 |
rs543530936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101398304 | AAATTTCTTTTTTTC[C/T]TTTTTTCTTTTTTTG | 8945 |
rs543546618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416907 | TAATTACTACATTAT[C/G]ACCAAAAGCAAAATC | 8945 |
rs543568396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407474 | GCTGGAGTGAAGTGG[C/T]GTGATCTTGGCTCAC | 8945 |
rs543569851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101361170 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 8945 |
rs543575782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487719 | GGGATCCTACCCAGT[C/T]GGAACACTGAAATTA | 8945 |
rs543580869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448156 | CAGCCATTCTCTAGC[A/G]TTCCAGTAACTTAAG | 8945 |
rs543592167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101430256 | CAGCTGCAACTGGAA[C/T]ATTGCGTTCAGCCAA | 8945 |
rs543592551 | in-del | -/AAATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101358526 | ATAGAGCTGATAGAT[-/AAATG]AAACAGTATAAAGGG | 8945 |
rs543593448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547204 | GCATCTGTATTTTAA[A/G]CTATTTGATTCATGC | 8945 |
rs543610490 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507372 | ATTTGCCAGGGGGTG[A/G]AGTTATTAAGTTTTA | 8945 |
rs543623027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540134 | TAATTTTAAGTCTAC[C/T]GCATTGACTTTTTCT | 8945 |
rs543628296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422506 | TTTTGGCTTTTGTTG[C/T]TATGGCTTTTGGTGT | 8945 |
rs543635004 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509533 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 8945 |
rs543644787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373351 | AATAGTCTACGCAAG[A/G]GACTGGGCTTGAGCT | 8945 |
rs543645066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399020 | TGCAGTGGTGCCATC[A/T]TGGCTCACTGCAACG | 8945 |
rs543674984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101382582 | CAGTTTGTTCCATTA[C/T]TGGAGATATTGTTTG | 8945 |
rs543695302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499272 | TGAGACAGGAGTCTC[G/T]TTCTGTCGGGCTGGA | 8945 |
rs543747100 | snp | A/G | 3.45131e-05 | 0.00415396 | intron-variant | BTRC | GRCh38.p7 | 10:101532442 | ATCAAGGTGAGGTCT[A/G]TTCAGTTGTAGAAAG | 8945 |
rs543772670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482241 | GGCCAGGCTGGTCTC[A/G]AGCTTCTGACCTCAG | 8945 |
rs543785751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387589 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG | 8945 |
rs543787823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545848 | AGAGAGAGCAAACCT[C/G]AGAGCAAAGAATATT | 8945 |
rs543793940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550414 | CTCAGCCTCCCAAGT[A/G]GCTGGGACTATAGGC | 8945 |
rs543849051 | in-del | -/AGTA | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101438538 | ACATTGTGTCAAATT[-/AGTA]AGTACAAAACTTTTG | 8945 |
rs543872245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538133 | CTGTTAACTGTCTTC[A/T]GTTTGGTTAAAGCTA | 8945 |
rs543894763 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101483376 | GAGACGGGTGGATCA[C/T]GAGGTCAGGAGTTCA | 8945 |
rs543943044 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393016 | TGCCCCAGGGCAGGA[C/T]TCTAATCTCCCACCA | 8945 |
rs543958648 | in-del | -/C | 0.0142736 | 0.0832652 | intron-variant | BTRC | GRCh38.p7 | 10:101505812 | ACATTCTTTGCTTGA[-/C]CCCCCCCCATAGATC | 8945 |
rs543960249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511553 | TTTGGGTTTTTTGTT[C/T]TGTTTTGTTTTGTTT | 8945 |
rs543961104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466354 | TTTTCTGTATTCTTT[C/T]TCTTGTGTAGCTGGA | 8945 |
rs543986088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390595 | CCTCGGTCTCCCAAA[A/G]CGCTAGGATTACAGG | 8945 |
rs544003472 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557646 | CCTACATCCCATTTG[A/T]TCAGTTTATAGGCAA | 8945 |
rs544003951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469957 | GTTGAATAAATATAT[C/T]GCAGTTTGTTTTCTG | 8945 |
rs544008353 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101448938 | AGGAATGGTATTTGT[A/C]ATTTTAAAGACCCGA | 8945 |
rs544010945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101458230 | ACATGAGTAGATCTC[A/G]GATATTTTATGCTAA | 8945 |
rs544035478 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101481960 | AAACACATAGCTGAA[A/C]AATTTTCTTTCTTGC | 8945 |
rs544047112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101503324 | AGTCATAGTCATTGA[C/G]TTGGAGCTTCATTGT | 8945 |
rs544069889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386767 | TTGTTTGTGGTTTAG[C/T]TTGTGTTTCTTCTAC | 8945 |
rs544080714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490455 | AACGAGGAACGAGAA[G/T]CTTAGATAAGTTAAA | 8945 |
rs544092643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440607 | CCAGTCTGTGGTCCC[A/G]GCTACTCGGGAGGCT | 8945 |
rs544144121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544855 | TTGAACTCAGGAGTT[A/C]AAGACCAGCCTGGCA | 8945 |
rs544166790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495176 | ATACATCCATGAAGA[G/T]AAAAATAAATGAGAC | 8945 |
rs544180581 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415286 | GCTGAAATGATCCTC[C/T]TGCTGCAGTCTCCCG | 8945 |
rs544193515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101456039 | AGCTGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 8945 |
rs544198837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485179 | TTTAAACCATTTTCA[A/T]CCAAAAAGAGACTTA | 8945 |
rs544227758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435454 | AATGCCATCATATAG[G/T]GTACATTCTTTGTGT | 8945 |
rs544234798 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101378879 | TTCAGTAATATATTG[A/T]AATGAGAAATAGGCG | 8945 |
rs544235866 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554400 | AGATGGTCAGGAGAA[A/G]ACACTGTTTTTGTTT | 8945 |
rs544256588 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101437038 | AAAATTATCCTGTGA[C/G]AGAAATGCTTCTCAT | 8945 |
rs544258815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101455153 | ACTCCTGGGCTTAAG[C/T]GATCCTCCCGCCTTA | 8945 |
rs544269794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428544 | TAGCAGATACCCTTC[C/T]TTTGAAGCCCAGTGT | 8945 |
rs544281352 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101396558 | ATAATGTTGGATTAC[A/G]ACAGCAAAATATGTG | 8945 |
rs544287658 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554585 | AAGTTTGGCACACAG[C/G]GTTTATTAATGGGGC | 8945 |
rs544301400 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101438285 | CAAAAATTAGCCGGG[C/T]GTGGTGGTGGGCGCC | 8945 |
rs544303821 | in-del | -/T | 0.379354 | 0.213933 | intron-variant | BTRC | GRCh38.p7 | 10:101362399 | CAGAGGTGCAAGAAA[-/T]TTTTTTTTTTTTTGA | 8945 |
rs544315304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477875 | GGGTGGCCTCAAACT[C/G]CTGAGCTCAGGCGAT | 8945 |
rs544339669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364016 | TCTAAACTTGGCTTA[C/G]TCAAAGTCAAAAGCC | 8945 |
rs544353468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478754 | CCACTGTACTTCCAG[C/G]TGGGGTGACAGAGTA | 8945 |
rs544359597 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423206 | CACATGAGCCACCTT[A/G]CCTGACCCTCTCTGG | 8945 |
rs544383071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399035 | TTGGCTCACTGCAAC[A/G]TCCGCCTCCTGGGCT | 8945 |
rs544390944 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429718 | CACAGACCCCAATCC[A/C]TCTGGAAAGATGAAG | 8945 |
rs544413761 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517661 | TGTGATTATCCTTTA[A/G]AGAAATACTTTCTTC | 8945 |
rs544471206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551523 | TACCCAGGTGGTCCA[C/T]ACATATTGTGGTATA | 8945 |
rs544475886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520802 | GTCTCTACTAAAAAT[A/G]TAAAACTTAGCCAGG | 8945 |
rs544492309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403874 | TGCTGGGATTATAGG[C/T]GTGAGCTACTGCACC | 8945 |
rs544498399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101461500 | TAAATGTTTTTTTAA[A/G]TCCTATGCTACTTTT | 8945 |
rs544519705 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464016 | AGTTACAATTTTAAC[G/T]GTTTGGAGAATCAAC | 8945 |
rs544525412 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553753 | GGCCTCCTGCCTGCC[G/T]TCTCTTTGTTTCTGT | 8945 |
rs544533771 | in-del | -/CTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101368333 | GATGCTAGCACCATG[-/CTT]CTTGTACAGCCTGCA | 8945 |
rs544565220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445143 | TGGTGCCCTTGGAAT[G/T]AATAAAAGGAGTCAT | 8945 |
rs544579457 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101505386 | GCACTCTGGGAGGCC[A/G]AGGCGGGCGGATCAT | 8945 |
rs544624581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458972 | GTAGTTTTAAATTTT[A/G]CTTAGGTTTTTGAGA | 8945 |
rs544624915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449626 | TTTTAAAAGATTCCT[A/G]TAGATTTAAAGGTAA | 8945 |
rs544660437 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493755 | GATAAAAATTAAAAA[C/T]GCCTCAATTAGCAGC | 8945 |
rs544678820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497159 | AGCACCATTTATTGA[A/G]ATGTGTAGTTCCCAT | 8945 |
rs544679678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389225 | TGGAATCATCATTGG[C/G]TCCTCACTTTTTCTT | 8945 |
rs544685344 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523696 | TATGTGTATTTGCCT[A/G]TAAAGCTTTGATCAT | 8945 |
rs544735948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547934 | ATGGATGCAGTAAAA[A/G]CATTTGACAAAATCC | 8945 |
rs544785860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530563 | ATTACTAACAAAATT[G/T]CCAAAAGATGAGGCC | 8945 |
rs544798655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424893 | TTGGAGTCTGAGTGA[A/G]TCTCACCCAGGTAGA | 8945 |
rs544810100 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452941 | AGCTTCTGAACTTAA[A/G]TGACCTAAGTTTTCC | 8945 |
rs544820796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416699 | CTCTCTGCGTGTAAA[A/T]TTTAGGAGTCAGGAA | 8945 |
rs544823353 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101521506 | TCTGTGGTTTTCCAC[A/G]TAATTGCTAATAGAA | 8945 |
rs544838202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470610 | GCTGGGATTACAGGC[A/G]CGAGCCACCGCGCCT | 8945 |
rs544843920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101462192 | TTGGCCTGGCCATAG[C/T]CATCACTTTCAATCA | 8945 |
rs544846543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356631 | TTATTGACCTTGCCT[A/G]CTGTTTTGGCTGCCA | 8945 |
rs544893776 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420005 | TGCTATTAGGTTGCT[C/T]CTAGGCCCTCTCAGT | 8945 |
rs544910724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101357310 | GCCAGGCCTGGTGGC[A/G]CGCACCTGTAGTCCC | 8945 |
rs544925965 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414626 | TGTCATAGGAGATGA[C/T]AGGTCCATAGATGTT | 8945 |
rs544930465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454228 | TAGTGGGTAGAGGGA[A/G]CTACAAAGACTTTTC | 8945 |
rs544936784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458399 | GAATTTTGGGAGTGG[A/T]GGAATTTTTCATTTT | 8945 |
rs544956523 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398396 | CAAGCTCTGCCTTCC[A/G]GGTTCACACCATTCT | 8945 |
rs544978463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508730 | CCACCCTGGCTAACA[C/T]GGTGATACCCCGTCT | 8945 |
rs544995673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400943 | CAAAAGCTGAATCTT[A/C]CCACCGAACACTGCA | 8945 |
rs544999696 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101511087 | TATTTCAAAACCTCC[A/C]GGGGCTCTCCTTTAC | 8945 |
rs545032230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499427 | AGGTGGGGTTTCACC[A/G]TGTTGCCCAGGCTGC | 8945 |
rs545066291 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101378629 | TCCCATGTTCAAGCG[A/G]TTCTCCTGCCTCAGC | 8945 |
rs545069768 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101509549 | GTGAGCCACCGCGCC[C/T]AGCCTTTTTTTTTTT | 8945 |
rs545086748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101354960 | TAGAATTACAAATGT[C/T]AGGGAGGGGTACATA | 8945 |
rs545087987 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101383961 | CAAAAGTGATTCTTC[C/T]GTCTCAGCCTCCCAA | 8945 |
rs545089151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101410443 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8945 |
rs545111517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355551 | AGATTTTAAGCTTAA[C/G]AGGTGGCCTTAGGGA | 8945 |
rs545122073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510571 | AAACCTGACAACAGC[C/G]TCTAGAGAGTATAAT | 8945 |
rs545127065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460241 | TTTAAAAAAAAAAAG[A/T]TAAACATACAACTTG | 8945 |
rs545145928 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422807 | TATTTCTGAGGGCTC[-/T]GTTCTGTTCCATTGG | 8945 |
rs545157366 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485208 | TAAAAAAAAAAGTCC[A/G]GACCCCAGCCCAGAA | 8945 |
rs545157430 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101451088 | AATTTAAAGGGAATG[G/T]TTGTTAGACTTAAAA | 8945 |
rs545191996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482557 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 8945 |
rs545196865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465022 | TTTTTAAGGTAGGAC[A/G]TAGTATATAAGCTGT | 8945 |
rs545198658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401928 | AAAGAAAAACAGAAT[A/G]TTGATGTTAGAAAAA | 8945 |
rs545203980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483487 | AATCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGA | 8945 |
rs545205227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407633 | CGAGCTCAGGCAATC[C/T]GCCCACCTTGGCCTC | 8945 |
rs545209258 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470404 | GTGACACAATCTCGG[C/T]TCACTGCAACCTCTG | 8945 |
rs545244880 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101454806 | AATCCTTTCAACCCC[A/G]AAATTTCAAGATCAT | 8945 |
rs545259656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360159 | TCCTGGGTTCAAGCA[A/G]TTCTTGTGCCTCAGC | 8945 |
rs545259665 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101368517 | CAGGGTCTCACTCTG[C/T]TGCCCAGGCCGGAGT | 8945 |
rs545259725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434235 | AAGGGAAAGATATTT[C/T]AATACCATTTTCAGG | 8945 |
rs545282172 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101357520 | CATGGAAGAACTATC[A/C]TTTTAATCAAACGGG | 8945 |
rs545289447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101474891 | TAAAATGTTTTTCCT[A/G]TCTGCAAGAGGGTTT | 8945 |
rs545309973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362112 | ATTACAGGCACGTAC[C/T]ACCACACCCAGCTCA | 8945 |
rs545317639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376373 | ACAAATCTCATGGCC[A/C]AGGCTTGGACTCTCT | 8945 |
rs545330449 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101396645 | TCATAGCTCATAATC[A/G]TGTTGGTATTGCTGT | 8945 |
rs545353322 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101432519 | TTTTTGTTTTGTTTT[A/G]TTTTTTAACCTTTTC | 8945 |
rs545401380 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101397741 | CCCTGTTACTGTATC[A/G]TTTTAGTCTTAAGTG | 8945 |
rs545406547 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101550571 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCTCTTT | 8945 |
rs545429646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522625 | GGGGTTTCACCATAT[G/T]GGCCAGGCTGGTCTC | 8945 |
rs545464171 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547794 | AACAATGTATGAAAA[C/G]AATTATACACTGTGA | 8945 |
rs545492423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358428 | TTAAAAACAGGATAA[A/G]TATATTCTTGTCCAG | 8945 |
rs545509582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519824 | AACATGGAGAAACCC[C/T]GTCTTTACTAAAAAT | 8945 |
rs545513681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411303 | CTGGCCATTTCTGGC[A/C]CTTTTTATAGTTTTG | 8945 |
rs545515115 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101551803 | TTCCTCAGCCAGGTC[A/G]CACAGGCTGTGTGCC | 8945 |
rs545517895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460683 | GTTTTTTATCTCTCA[G/T]TATCTTTCAAAATGT | 8945 |
rs545518377 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101532225 | GAGCCATTGATTGTC[A/C]TTAAAGCCTAAAAAG | 8945 |
rs545560216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451749 | AGTAATCAGTGTCAT[C/T]GTGCCTTTAAATCGT | 8945 |
rs545572410 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356269 | CTCCCAAAGTGCTGG[A/G]ATTTCAGGTGTGAGC | 8945 |
rs545577669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472562 | CTCATGCCTATAATC[C/T]CAGCACTTTGGGAGG | 8945 |
rs545589727 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490043 | TTAAAGTTCTTATGC[A/G]TGGGACCAGTTGTAT | 8945 |
rs545591504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493247 | AAGTGAAAAATTTTT[A/T]AAAAGTACTAAAATC | 8945 |
rs545601407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542898 | TCGTTGTTTTTGAGA[C/T]GGAGTTTCTCTCTTG | 8945 |
rs545624696 | in-del | -/A | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405581 | TACTGGAGGAATAAT[-/A]AAAAAGATAAATTCA | 8945 |
rs545635625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486790 | TACAACATGAAATAT[A/G]TATTCTTTATGACCA | 8945 |
rs545636513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377056 | TTGTATCACTCCCCC[A/G]CAAAAAACTCTTATA | 8945 |
rs545653694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372308 | TTCACTCAGGCTGCA[A/G]TGCAGTGGCGCAATC | 8945 |
rs545657171 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101434526 | GTGACTTTGGGTTAG[A/G]CAGAGATTTCTTAGC | 8945 |
rs545662322 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527506 | GCCTGTAATCCCAAC[A/G]GTTTTGGAGGCCAAG | 8945 |
rs545698078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369933 | CCACACCCACTATAT[A/G]GATGCCGTCCTTGAC | 8945 |
rs545705559 | in-del | -/TTT | 0.499995 | 0.00159744 | intron-variant | BTRC | GRCh38.p7 | 10:101389611 | CTTTTGCCAAACACC[-/TTT]TTTTTTTTTTTTTTT | 8945 |
rs545723880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101536199 | AATCTGTATCTCTTT[C/T]AGTTTGGTGACTTCA | 8945 |
rs545726058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417564 | CAGGGTTTTTTTCCC[A/G]CTATAGAATTAACTT | 8945 |
rs545726170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426921 | CTTCCAGTGCCTCCT[C/T]GATTTTCTTCCACTA | 8945 |
rs545739503 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101380864 | CAGAGTGTACATAGA[A/C]AAATCTAGATAGTAT | 8945 |
rs545749327 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438217 | AGATCACAAAGTCAG[A/C/G]AGATTGAGACCATCC | 8945 |
rs545775776 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445902 | ATGTTTAATTAACCC[A/T]GCAATGGGCTGCGTT | 8945 |
rs545801945 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101414029 | TTAAGTGTACAATTC[A/G]GTAGTTTTAGCACAT | 8945 |
rs545809880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101422333 | GTTTGTTTTTTTCTT[A/G]TAAATTTGTTTGAGT | 8945 |
rs545833386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498646 | TTTAAAGTTTAGTGG[A/G]CACGTCCTAATACAG | 8945 |
rs545841473 | in-del | -/ACCA | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101443988 | ATTAAGTACTTATAT[-/ACCA]GTCACTGTGCATATA | 8945 |
rs545865117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541495 | TCGATCTCCTGACCT[C/T]GTGATCCAGCCACCT | 8945 |
rs545866277 | in-del | -/T | 0.495016 | 0.0496707 | intron-variant | BTRC | GRCh38.p7 | 10:101358260 | CCACTATGCTGGCTA[-/T]TTTTTTTTTTCTTTT | 8945 |
rs545877696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463460 | GCTGGGATTACAGAC[A/G]TGAGCCACCACACCT | 8945 |
rs545884503 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499568 | ATTATGTATCTTACC[A/G]CCTCCATAAATAAAG | 8945 |
rs545928941 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101371910 | CACACCTCACACATG[A/G]GGCTGAAAACCCAAT | 8945 |
rs545946445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455550 | CGTAAGGGGATAAAG[C/G]CTTCTCAGAGAAGGT | 8945 |
rs545949942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | BTRC | GRCh38.p7 | 10:101515890 | GATGGTTTTCAAAAA[A/G]TGTATTCTTTTTTAA | 8945 |
rs545960829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437793 | GTTCCCCAAAGGTGC[A/G]GTGTGTTCTTTTATA | 8945 |
rs546005623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547008 | ATAACTTACTAACTC[A/G]TCTATGAAGCATTAC | 8945 |
rs546009804 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555512 | GGAATGAAGTTAAGT[G/T]GTCTGAAAAACTTGA | 8945 |
rs546026602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379825 | AGCCAGGAAAAAAGG[A/G]ACAGAAAATAAAACT | 8945 |
rs546073113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406641 | TGGGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTC | 8945 |
rs546092988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547721 | TAATGTGCCAATAAA[A/G]TGTAGTAACTCTGAA | 8945 |
rs546116972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549104 | ATATGATTATATTTA[C/T]ATGAAATTCAGTAAG | 8945 |
rs546157049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381709 | TGATAACTCATATAT[A/C]CCTCACCTGAATTAT | 8945 |
rs546163633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431297 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 8945 |
rs546217991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374403 | TCCAACAACGATAGA[C/T]TGGATTAAGAAAATG | 8945 |
rs546219182 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101469469 | TAAATATGTTATTAC[A/T]TATTCATTCATGAAG | 8945 |
rs546225759 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381394 | CATTGTGCTATACTA[A/G]CCATGTTCCTTAATT | 8945 |
rs546257657 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101427119 | TTTTTCTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 8945 |
rs546262151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490351 | AATGTATTCAGCCCC[A/C]GTGTTCAGGCACTAT | 8945 |
rs546266358 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101505614 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAATAA | 8945 |
rs546360405 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101467453 | GAAAACCCATTCCCT[A/G]TCTGCCGTTGCTTTG | 8945 |
rs546361488 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502094 | AGAGTTTTTCTGCCT[A/G]TTTCTGAGAGAAAGG | 8945 |
rs546365205 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514262 | TGCCAATTTACTGAC[-/T]TTTTTTTTCCTTTTA | 8945 |
rs546386163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101392216 | AACTCTTGACCTCGT[A/G]ATCTGCCCGCCTTGG | 8945 |
rs546391497 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101354648 | ATTCACGACTGGGGA[A/C]GGGAGCGCGGGATAG | 8945 |
rs546398520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392819 | GTAAGCTTCCGCACC[C/T]GACCAATTAAAAGTT | 8945 |
rs546400110 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101408933 | GGGCGCATGAAAGCC[C/T]AGCTATTTGGGAGGC | 8945 |
rs546422514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506650 | TTAAAATTCCAAGCT[C/G]AGATTCAAAATTGAC | 8945 |
rs546438043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101456415 | AAGAAAAAAAAGGAA[C/T]GAGTAAAAACTGACT | 8945 |
rs546439844 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439886 | AAGAGATGCAGTGAC[A/G]TAGTTTGTTAAACTG | 8945 |
rs546447344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101433447 | TGTTTAAGAGCTGAA[A/G]GATGAATAGGAATTA | 8945 |
rs546463092 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101518259 | ATGTCCCATATAGTT[C/T]TAAAGGACCACATAG | 8945 |
rs546480626 | snp | A/G | 0.00415042 | 0.045365 | intron-variant | BTRC | GRCh38.p7 | 10:101479480 | ATATTGCTCATCAAT[A/G]TATATTACACCACAC | 8945 |
rs546524619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439451 | ATTACAATGAGAGAA[A/C]GAGAGACTGACATAC | 8945 |
rs546533593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434419 | AACGGTTATACTGCA[C/T]TATATACATAAATTA | 8945 |
rs546550977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376063 | AGTTGCAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 8945 |
rs546561546 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101544059 | GGACTACAGGCGCCC[A/G]CCACCACACCCAGCT | 8945 |
rs546574774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483708 | TTCTTTCTCCTGGTT[A/G]TGGCCCTGTGTTTCA | 8945 |
rs546623867 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101394241 | GAAATGGTTCGAGTA[C/T]GAACTCAATTATTTT | 8945 |
rs546634953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549051 | GAGCGAGACTCTGTC[G/T]CAAAAAAAAAAAAGC | 8945 |
rs546635364 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101494815 | CTCAAATTCTGTCTG[G/T]ATTGCAGAGGATTAC | 8945 |
rs546649348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536393 | ATAGCAGAAAGGAAA[G/T]AAATTACATTGAAAG | 8945 |
rs546669290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386210 | ATTTCCAGGACCTTT[C/T]TATTTTTATAAGTTT | 8945 |
rs546679236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362200 | TCCTCCTTGTGATTC[A/G]CCCGCCTTGGCCTCC | 8945 |
rs546680976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101370403 | ACAGGTGTGAGCCAT[C/T]GGGCCCGCCCCTTCT | 8945 |
rs546682152 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101418711 | ATTATTATTATTATT[A/T]TTTTTTTATTCTGGG | 8945 |
rs546706964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495377 | TGAACTTTGCAAAAC[A/T]GGCATAGGCAGCCTA | 8945 |
rs546711806 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101401488 | GGTATAGAAAACATG[A/T]AGCATCAAAGCAGTG | 8945 |
rs546713249 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101364694 | AAGTACTACACCAAA[A/C]TGTTAATGTGGTTAT | 8945 |
rs546727909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527541 | GAGGATCGTTTGAGC[C/T]CAGGAGTTTGATACC | 8945 |
rs546765033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101509816 | GTCCTTCTGCCCTGG[C/T]GTCCCAAAATTCTGG | 8945 |
rs546796601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460369 | TCATTAATTCAATTA[C/T]ATCCTTCCTCCATTT | 8945 |
rs546797585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450504 | TTAGTTGAGCTTGTT[C/T]ATCTTAAAAGAGCAG | 8945 |
rs546814043 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101424360 | TAAATTGGGATTCTT[-/AA]GAGGCAATCATTGGA | 8945 |
rs546821877 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101516723 | TCCTTAGGCAGTTTT[A/C]CCTAACAGTCTGATA | 8945 |
rs546824637 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101537484 | AGTGAGCCAAGATTG[C/T]GCCACCACACTCCAG | 8945 |
rs546828688 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436514 | TGGTGGTACTCACCT[C/G]TCCCAGCTATCTGGA | 8945 |
rs546830405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101442525 | AAATTGAAAAGGAAA[A/G]AATGTGATAAATTTC | 8945 |
rs546838899 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101391290 | ATATATTCAACTGGG[A/C]GAACTACTTTTTTGA | 8945 |
rs546884345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451993 | TGTCACGAGTTCATA[A/G]ATCAAAGGAGTTTGT | 8945 |
rs546910646 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101510966 | CTCTGCTTTTGCAAC[G/T]TGCTCTTATTATCCC | 8945 |
rs546914612 | in-del | -/CCACTTCTGTTACTGGCACCG | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101552771 | CTTTCCTTGATTCCC[-/CCACTTCTGTTACTGGCACCG]CCATGCTCATGGCCA | 8945 |
rs546919244 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375320 | CCATATAAGATGCAC[C/T]TGCTTCCCCTTTGCC | 8945 |
rs546921236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452576 | TGTCGGACAGTGTGG[C/T]GGGGAGAAAGCCTGC | 8945 |
rs546934176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101492618 | TAGTATTAATATAGT[A/G]TCATTTTGGACTTTA | 8945 |
rs546995727 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101461384 | ATTGTTGTTTTTTTC[C/T]CCCTCCTAAGTATAT | 8945 |
rs547000184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502367 | TGGGAAAACATTGTA[A/G]CAATAGCTCTGAAAG | 8945 |
rs547008250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394487 | TAAGGATTTTTGTCT[A/G]TTTAAAGACTCAGTT | 8945 |
rs547014594 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101443775 | ATTGTCCTTAGGGAC[A/G]TTTTACTGATTTAGA | 8945 |
rs547024597 | snp | A/C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459872 | GAGATGACTATTTTT[A/C/G]ACTTTATAATTCAGT | 8945 |
rs547031784 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101435793 | TCTTCAAAGTGGTTG[G/T]CACAGGAATACCCAT | 8945 |
rs547035903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378468 | GGTGTTAGTCATGTC[A/T]GTACTTTATTTGCTA | 8945 |
rs547058880 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467038 | ATAGTGTGTATTAAC[A/C/G]AAACAACCACAACAA | 8945 |
rs547062848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500726 | GATTTTAAATTATTA[A/G]TTTTAAAGTCAGCAT | 8945 |
rs547075057 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101545102 | TCTTTCAGCACTTTA[A/G]TGATGTCATTCCATT | 8945 |
rs547098497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448269 | TTGGAGAAAAAACAT[C/T]TTTTAAAAATTTGTT | 8945 |
rs547098577 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378850 | CATGGGAAAACATCC[G/T]CTTTGAAGCAGTATT | 8945 |
rs547101798 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493182 | TTATTTTCACTTGCA[C/T]GGGTAGGTTCTCAAA | 8945 |
rs547108157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498773 | AGGCAGGCAGATGAC[C/T]GAAGGTCAGGAGTTC | 8945 |
rs547127481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410844 | TATTTTCAGTTTTCT[A/G]CATTCCTATCCTTTG | 8945 |
rs547135491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439760 | AGATAAAGTTGGGTT[A/C]GTGTATTATTAATAG | 8945 |
rs547143869 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101468397 | TACCATTAAAAAAGG[C/T]GGGGGGTGGGGTGGG | 8945 |
rs547149812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382076 | CAACCTTCGCCTCCC[A/G]GGTTCAAGTGATTCT | 8945 |
rs547163073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428014 | GCTTTTTTTACCCTA[C/T]TTTCTCCATTCTCTT | 8945 |
rs547166237 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406474 | CGGCCTACTGCTTAT[A/G]CTCTTTGTTCCGAGG | 8945 |
rs547202099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463755 | ATTTGATACTCAGAT[C/T]TCAGTGTTTCCAAAG | 8945 |
rs547206970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101355173 | ATCATTTTCTGGGAA[A/G]GGAAAGGCCGTGGAG | 8945 |
rs547214015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519395 | CTCAGCTCATTCTTG[C/T]AGTAGGCAGAATTCA | 8945 |
rs547234299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402133 | AAGGCCTTTTTAAGG[C/T]TGTATGCTAGTCTCA | 8945 |
rs547248120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472081 | TGCAGAATGGTATTT[A/T]AAAACCAAGATTCAA | 8945 |
rs547250584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520108 | CATAGCACTACCTAC[A/G]TTATATTTTCTAAGT | 8945 |
rs547270396 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438388 | CGAGATCGCGCCACT[A/G]CACTCCAGCCTGGGC | 8945 |
rs547287017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101464345 | CCAGCACATACAGAT[A/G]GACCAGCAGGTCACA | 8945 |
rs547294033 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101511981 | TTATCTTTCTTTGTT[A/T]TCTTCACAATCCTTA | 8945 |
rs547294463 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556932 | AGTGTTACCTCCCCT[C/T]CTAACCCTTCCCCTT | 8945 |
rs547309603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358781 | GTAGAGACTGCCAGT[C/T]TTCTAAATCCTAGAT | 8945 |
rs547345859 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101393791 | CTCCTGGCATGTGCA[C/T]ACCCTGCTTTGGAAA | 8945 |
rs547347895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402907 | GGTCTAACAATAATG[A/G]TATCAGACTAGTAAT | 8945 |
rs547385013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516942 | CATTTTAAAAGGCAA[A/G]TATATAAAAAATGAT | 8945 |
rs547403701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399395 | TTTAATGGTAGCAGG[A/T]CATGTATGACTCATG | 8945 |
rs547410725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398342 | GAGACGGACTCTTGC[C/T]CTGTCGCTGGAGTAC | 8945 |
rs547416858 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556868 | CGCTCTTAGCTCCTG[A/T]TTGGTTGTGTGTTTT | 8945 |
rs547429680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101407762 | ACAGTCTCGTTCTGT[C/T]GCCAGGCTGGAGTGC | 8945 |
rs547452015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517771 | CTTTTTTCTCATACT[C/T]ATATCCAGTCGATCA | 8945 |
rs547479600 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557732 | AAGGCACCCTTGACT[A/G]TCTGGGATATGACAT | 8945 |
rs547479608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549228 | CTGCTTGGTCTTGAG[C/T]TCAAGACCAGCCTGG | 8945 |
rs547502538 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353316 | AATATTTATATGCTT[G/T]ATTTGCTGGAGGCCA | 8945 |
rs547539655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101490518 | GAGTCAAGTTTTGAA[C/T]TAAGATCTGACTTCA | 8945 |
rs547541039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549625 | AGGCTGAGGCAGGAG[A/G]ACGGCGTGAACCCGG | 8945 |
rs547571850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374744 | ATATGTATGTAACCT[A/G]CACAATGTGCACATG | 8945 |
rs547612587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449890 | ACCTACAGTGGTATA[A/T]GATGCCTGCTTTGCA | 8945 |
rs547636352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515441 | GTATCTCTCCATTTA[C/T]TTAAGTCTTTTTAAA | 8945 |
rs547645406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368129 | GTTCCTCATGAAGGG[C/T]TTGGTGCCATCCTTT | 8945 |
rs547646425 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555400 | GAGACATGTCCAGTA[C/T]ATCACAAAGGAGATC | 8945 |
rs547668425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455864 | ATGATTCTAATGGCC[A/G]GGCATGGTGGCTTAC | 8945 |
rs547677676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101523561 | TGTTGTTTTCCAATT[A/G]TAGAAGTTATAGGAA | 8945 |
rs547702514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447506 | ATACCACAATTAGCT[A/G]TTATGGTATTCACTA | 8945 |
rs547747992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406898 | CTTTTAATTTATTGG[C/T]ATACATTAATAGATA | 8945 |
rs547757576 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101473822 | AGGCTGGTCCTGAAC[G/T]CCTGAGCTCAAGCTA | 8945 |
rs547758990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529728 | CATCTACCTTCCTGA[C/T]AGGAAATTTTCTCAA | 8945 |
rs547769911 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101382726 | CACGCAGTAGTTTTA[C/T]CATCCATTGGTGATT | 8945 |
rs547783649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465369 | ATTGTTGATAGGACA[G/T]AACTACTGCATGTTA | 8945 |
rs547789480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101408909 | AAAAAATTAGCTGGG[C/T]GTGGTGGTGGGCGCA | 8945 |
rs547789610 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101412501 | GATGGTAGGAAGATA[A/T]GTTTGATACCAATTA | 8945 |
rs547804686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403410 | CTACTTAGTCATGGT[A/G]TATATTCCTTTTTCT | 8945 |
rs547822337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466490 | GGCTCAGGGCATTAC[A/G]TTTTCCTCCCCCATG | 8945 |
rs547832264 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379321 | TTAGGTTTATATGTG[C/G]TCATGTTACAAAGGA | 8945 |
rs547832683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101495446 | AAAATAAAAATCACC[A/G]TATTGCATTTAACCG | 8945 |
rs547867703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420333 | TCGCTCCATTTCTCA[C/T]CCCATACTTCATATG | 8945 |
rs547909560 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536486 | GTGTATTGTTATAAC[A/G]TTCCAGGCTTAGAAA | 8945 |
rs547910276 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101364124 | ATTTAGAGAAGAATG[A/G]TAAGATGCTTATTAT | 8945 |
rs547911307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458536 | CAGGAAATTAATATT[A/G]ATACAGTGTTATTAG | 8945 |
rs547914325 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101403950 | TCTTTCTTTCAAGAG[A/T]GTTTTTAGTTATTGG | 8945 |
rs547929310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481821 | AATCTAATTTAATGA[C/T]GATGTCTATCATTTC | 8945 |
rs547944420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101512346 | AAGCCAAATGGAATC[C/T]TTAGATATCTTTTAT | 8945 |
rs547965540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377296 | GACTGTTTATTCACT[C/T]CTGAAGGACATTTGG | 8945 |
rs547972964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356905 | GGAGGCCGAGGCAGG[C/T]GGATCACGAGGTCAG | 8945 |
rs548004453 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484661 | CGTTCTTCACACAGG[C/T]GCCTCTGTCAGGTCT | 8945 |
rs548025920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370617 | TCCTTCCCTCCCTCC[A/C]TCCCTCCCTTTCTCC | 8945 |
rs548027901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378103 | ATGATTTTAATAATT[A/C]TTATTCAGGGAAGTA | 8945 |
rs548030429 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101354762 | CTGGTGAGAGGCTTA[C/T]AGTTTTGTAGAATGA | 8945 |
rs548031322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101484629 | ATACTGTTCCACAAG[G/T]AGCATGTCATATGGT | 8945 |
rs548057048 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101466059 | CTGGGAGGATACATG[A/G]AAGTACTCATTACTT | 8945 |
rs548116017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528712 | TTTTTTAAAAAAAAA[C/T]TTACTCCATCAGTTT | 8945 |
rs548132879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476425 | ATGTAAGATATTAAC[A/T]TATGGAGAAGCTGGG | 8945 |
rs548149610 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434344 | AATCCATTGGTCTCA[G/T]TTTTTTTCAATAAAT | 8945 |
rs548153639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418766 | TGGTACGTAGGTAAA[A/C]ATGCCATGGTGTTTT | 8945 |
rs548206154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101456364 | AGATGATTCAAAGAA[A/G]AAGTTTATAGACTGA | 8945 |
rs548219542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470161 | TTGCATTGTTTGCCT[G/T]TTTATTATTGAGTTG | 8945 |
rs548224488 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101494141 | ATTTCACCCCTAGTT[C/T]GAGCTGCTCTTAGAA | 8945 |
rs548228305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538241 | CTATTCTTCCCTGCC[A/T]TCTCTTACATTTGCT | 8945 |
rs548231079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520941 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTG | 8945 |
rs548261778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101471220 | AACCTTGCACTTTCT[A/G]TTAAAAAGCAGTCTG | 8945 |
rs548272666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512996 | GCCAAATCAATTCTA[C/T]TGCAACCAGTAACCA | 8945 |
rs548300405 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101453854 | TTTGTCTGTAAAGGG[A/G]CAGATAATAAACATT | 8945 |
rs548343000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540264 | ATTTTCAGTTTGTAT[A/T]TTGGTCTATGATCCA | 8945 |
rs548378158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101480018 | TTAAATATTAGAGAT[C/T]TGATGCTTTTTATAT | 8945 |
rs548379560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544968 | TGAGGTGTGAGGATC[A/G]TATGAGTCCAGGAGA | 8945 |
rs548388973 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101426863 | ATGGTTAAAAGTGTC[A/G]CCTGCCCTCTTGTGA | 8945 |
rs548408280 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101462804 | GCAAAAACAAGAAAC[A/G]CAAGTTCTTATGATG | 8945 |
rs548414812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366165 | TGTGCTGGAGTACCA[C/G]ATTTTCTGTTAAGTA | 8945 |
rs548428504 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101469587 | TGGACAAACCTCTGT[-/A]AAAAAATTTACTCCT | 8945 |
rs548429699 | in-del | -/AC | | | intron-variant | BTRC | GRCh38.p7 | 10:101522366 | TTAAAAAAAAAAAAA[-/AC]AAAAAAAAACAAAAA | 8945 |
rs548430832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427951 | AAAGCATTCTTAATA[C/T]GTATAAAGAAGTAAT | 8945 |
rs548451126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477334 | AGCCCTCCTTCCAGA[C/T]GATTCTGATGCGCAC | 8945 |
rs548459881 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554816 | CTGGGAGCACACAGA[A/G]TACTATTAATGTGCA | 8945 |
rs548482042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514125 | TAAAACAGGATTTTT[A/T]AAAAATTATTATTGA | 8945 |
rs548508931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395974 | ATGATGGGAGAAGGT[C/T]TTGTATTTTTGTTTT | 8945 |
rs548512164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437875 | AAACACCTATTGTCC[C/T]TTACCCACTCTCTGC | 8945 |
rs548512911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454633 | AAAAAAACAGAAAAA[A/T]TAGCCTGGTGTAGTG | 8945 |
rs548524812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101505598 | GCACTCCAACCTGGG[C/T]GACAGAGCGAGACTC | 8945 |
rs548551886 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101418570 | CCCAAAATGACAGCA[A/T]GATATACCTTGGCAA | 8945 |
rs548553665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446489 | TGTAATTGTGACTAA[A/G]AATTATAATGAGACT | 8945 |
rs548563033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546384 | GGTCAAGAAGAAATT[G/T]CAAGATAAATTGAAA | 8945 |
rs548575360 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101388700 | TTTGCCATGTTGCCT[A/C]GGCTAGTCTTGAACT | 8945 |
rs548584909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380301 | TATAAATAGAGCAAA[G/T]ATTTTGGAAATTATA | 8945 |
rs548593160 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101409028 | CACTCCAGCCTGGGC[A/G]ACAAGAGCAAAACTC | 8945 |
rs548605250 | snp | A/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407340 | TTGACAATGAGACCA[A/T]GTCTCTTACAAAAAA | 8945 |
rs548634424 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101413383 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAGGCTC | 8945 |
rs548642151 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101487829 | GCTGCACAATGCCAG[C/G]CTCAGTTTCTGAAAA | 8945 |
rs548655186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474573 | ATTTGAGGGGAATTT[A/C]TATGTAATTTTTTAG | 8945 |
rs548684164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357869 | ACAAATAAATGATAT[C/T]GAAAGCAACGGTTTA | 8945 |
rs548708981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413639 | GGTTTTGATGCAAAA[G/T]ATGAAGATGTCCCAG | 8945 |
rs548717946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542518 | GAGGAATTTTTATGT[C/T]TCCCACTATAGTTTT | 8945 |
rs548725412 | snp | A/C | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352261 | AATTCAAGAACAAAA[A/C]TTTTTATTAACTGAA | 8945 |
rs548739554 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | BTRC | GRCh38.p7 | 10:101531721 | GCGAGACTCCATCAA[A/C]AAAAAAGAAAAGGAA | 8945 |
rs548742232 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101425801 | GGCAAGAGAGTGAGA[-/CT]CTGTCTCAATAAAAG | 8945 |
rs548746852 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101474557 | TGGGTGTTAGCCATA[G/T]ATTTGAGGGGAATTT | 8945 |
rs548758698 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387399 | GTCATTCTACAGTGC[C/T]GTAGAACACTAGGAC | 8945 |
rs548761175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368878 | ACAAAAGTTAGCTGG[A/G]TGTGGTGGCGGGCAC | 8945 |
rs548770502 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415564 | ATGTTATTTTGAGAC[A/G]GAGTTTCACTCTTGT | 8945 |
rs548771378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425335 | TTTTAAAGGCTAGTG[A/C]AGTCATTCAGTTGGA | 8945 |
rs548792945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504578 | CCTTTCCCCAATCCT[C/T]GGTCACTTTTGTCAT | 8945 |
rs548815316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382156 | CCCGGTTAATTTTTG[C/T]ATTTTTAGTAGAGAT | 8945 |
rs548824555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361414 | CCTGGCCAGCAATAT[C/T]TTAATATAGCACAGA | 8945 |
rs548827867 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101529004 | ATATGCTGTCTGCTC[A/C]GTAATGGTAACTCTT | 8945 |
rs548829661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495604 | GGTTTGCAAGTGAAG[A/T]TATAGTCTCAGGCTC | 8945 |
rs548874824 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101379259 | CTTCTGAATATGGTC[A/C]TCTTACCTGACACAT | 8945 |
rs548877415 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101397032 | TGGTCTCAAAGTCCT[A/G]ACCACAGGTGATCCA | 8945 |
rs548889407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547313 | TCAAAATAAATAAGT[A/G]AATATATGGTTTTTC | 8945 |
rs548902338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399223 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 8945 |
rs548909559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441586 | GTTGGTTCTACTAGA[A/G]AGTTTTTTCTTGGCC | 8945 |
rs548914861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101391522 | ATAGGCACAACCTTC[G/T]TAGTTCAGCCTTCCC | 8945 |
rs548922833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449220 | TATTGTTGAATTGTA[A/C]TAAAATGGTAATACC | 8945 |
rs548944777 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101476029 | TAGCTGTATAATCAA[C/G]GCTAACATCACCAGA | 8945 |
rs548982764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383985 | CTCCCAAATAGTTGC[C/T]GGTACCACAGGCTTG | 8945 |
rs548991246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502243 | AGGATGTTAGCTCTT[C/T]GGTAGAAATTGTTCA | 8945 |
rs549016189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101543065 | GTATTTTCAGTAGAG[A/G]CAGGATTTTGCCATG | 8945 |
rs549019819 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101481314 | GGGCCTTTAAAAATA[G/T]TCTTTCTTTCTTTTT | 8945 |
rs549037803 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505937 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTGTGT | 8945 |
rs549038604 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101483547 | GCAGTAAGCTGAGAT[C/G]GTGCCACAGCACTCC | 8945 |
rs549045704 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101375962 | GAAATGATGTGGCTA[A/G]AACCAGAGTAAAAGG | 8945 |
rs549051992 | snp | A/C/T | 4.95203e-05 | 0.00497575 | intron-variant | BTRC | GRCh38.p7 | 10:101534641 | TTGAGTACCATCTAA[A/C/T]TCTCATCTATCACTT | 8945 |
rs549066041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426130 | TTTCTCCTTCTTTTA[C/T]GAAATGCTTCTAAAT | 8945 |
rs549081036 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101509501 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 8945 |
rs549082228 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101369528 | CTTCTTATACTTTTT[C/T]TGCCCTAGCCCTGGA | 8945 |
rs549108165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393191 | GAGGGTGGTGTGCCC[A/G]GGGAGTCATGGCAGC | 8945 |
rs549120721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385218 | AAAAGAAAAAAAAAA[A/T]TAGCCGGGCGTGGTG | 8945 |
rs549141895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535648 | CAGCACAGCAAAGCC[C/T]TTTGTTGCCCTTCTT | 8945 |
rs549170354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101400116 | CATTTTTGTTACTTA[C/G]CAGGGAACATGACAC | 8945 |
rs549189033 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101507906 | TATCTACATCAGTGG[A/C/G]TTTACCAGCCTTGGA | 8945 |
rs549195828 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353965 | TAGCCTCAGTTTTTT[C/T]CCTGGGGGAAGTTCC | 8945 |
rs549196004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552069 | CCGTGTTACTTTGCC[A/G]TTTTTAATATTCTTC | 8945 |
rs549222168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354515 | GGGGCCCTGGAGGGA[A/G]AGGGGCGTGGGGACT | 8945 |
rs549245175 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362367 | ACCTGACCTGATGCT[A/G]TCAATTACAGGAGAA | 8945 |
rs549245801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101550102 | TAAAAACCAGGGAGG[C/T]AGTAAGGAATGCTCT | 8945 |
rs549254809 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468096 | CTTCAAAAAGGAGCA[A/C/G]TTTAATAACCGGCTT | 8945 |
rs549268973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383341 | TTTATAGGTGATGCT[A/G]CTGGTTCTGGGACTA | 8945 |
rs549283733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101355086 | GGGCAAAATGAGTAT[C/T]TAATAGGGTAAGCAA | 8945 |
rs549300690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432665 | GTTTGATAACTTGCT[A/G]GAAAGGACTTAGAAT | 8945 |
rs549370538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393749 | TTCCCTACACACTCC[C/T]CCACCCTGGAGGATC | 8945 |
rs549375145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101388953 | TTCCTGTCTACACTT[C/T]GTTCCTAGATGATCA | 8945 |
rs549395985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401967 | TTGTCTTATGCTCTG[C/G]AGTTCTTACCTCAAG | 8945 |
rs549412771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510167 | AGAAAAAGAAAGATG[C/T]TTTTACAAAGAAATC | 8945 |
rs549438519 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438689 | TTGTTTTGTTACTGG[G/T]AATAAACTACAAGGG | 8945 |
rs549467293 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472817 | TATGAAAAGCCTGAC[A/G]TTATTTATATCGTTA | 8945 |
rs549474862 | in-del | -/TTTTT | 0.433236 | 0.170072 | intron-variant | BTRC | GRCh38.p7 | 10:101509720 | ACCACACACAGCTAA[-/TTTTT]TTTTTTTTTTTTTTT | 8945 |
rs549493427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389475 | TATCTTCCTTTTGGA[C/T]TAAAGCTATGCATGG | 8945 |
rs549496200 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470197 | TCAACTGTATTGAAT[G/T]CTGGATACCATTCAT | 8945 |
rs549522600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396895 | GGAACCTCCGCCTCC[C/T]GGATTCAAGCAATTC | 8945 |
rs549524697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455756 | GTTAAGTTGGCTGTC[C/T]TATGGATGCTGTACT | 8945 |
rs549530320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470363 | TTTGAGACGGAGTCT[C/T]GCTGTGTCGCCCAGG | 8945 |
rs549533775 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453201 | TACTAATTTACCATT[A/G]AAGTTCACTATACTG | 8945 |
rs549539752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434892 | TGCCCACCTCGGCCT[C/G]CTAAAGTCCTGGGAT | 8945 |
rs549541365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444677 | ACCTCTTAAAAAGAA[C/T]ACAATTACAAATAGC | 8945 |
rs549551576 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501248 | TTTAAGTAAGAACAT[A/G]TGAAGAATGAATCTC | 8945 |
rs549569010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470956 | ACCTCCTGAAGAAAA[C/T]GTTGCTGCTGGACCC | 8945 |
rs549578589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526649 | GCCGAGTATGGTGGC[A/G]TGCACCTGTAATCCC | 8945 |
rs549597163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101362162 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGACAGT | 8945 |
rs549606179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356957 | AACATGGTGAAACTC[C/T]GTCTCTCTAAAAATA | 8945 |
rs549620058 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421379 | GTAACACTATTCTAG[A/G/T]TAGTCAGAATATCTA | 8945 |
rs549621296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409829 | GATAAGTATTTTTGG[A/G]CTGTTTTCAACCTTT | 8945 |
rs549655575 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556853 | AACCAGCACAGCTGG[C/T]GCTCTTAGCTCCTGA | 8945 |
rs549656751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519169 | CTGCAATCTCCACCT[C/T]CTGGGTTCAAGTGAT | 8945 |
rs549678961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460316 | GATACTCTTACATAG[C/T]ATGTATTGCCAGTCG | 8945 |
rs549691585 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514384 | TTAAGTTAATTTTTG[C/T]ATATGATGTGAAGTT | 8945 |
rs549724657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101415298 | CTCCTGCTGCAGTCT[C/T]CCGAGTAGCTGGGAC | 8945 |
rs549733327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401421 | TGTATAAATTTGCTT[A/G]CTAAGATGGTTGATT | 8945 |
rs549742949 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101533248 | TTAGAAATGCTTGAG[G/T]TAAGTTTACATTTTC | 8945 |
rs549751612 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416720 | GAGTCAGGAAATGCC[A/G]TAGGGGAAAAATTAT | 8945 |
rs549755043 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363168 | GTAATCCTGTGAGAT[A/G]GATTCAGTATTATTA | 8945 |
rs549784543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407136 | GCCGAGGTGGGAGGA[C/T]CAGTTGAGGCCAGGA | 8945 |
rs549821733 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101529380 | AGTATCATTGCATAG[A/G]AAGAAAGTCTTGGAG | 8945 |
rs549832147 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556177 | TGAGACCCCTACATC[A/G]TTCTGGTTTTTTTGC | 8945 |
rs549844004 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101383300 | TAGGCCTGGGTTGGG[A/G]TCTGAGAATTTGCAT | 8945 |
rs549871342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497562 | TAAAAAAAATTTATC[C/T]AGGCATGGTGGTGCG | 8945 |
rs549880606 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101538101 | TCCTCTTGATCCCAA[A/C]GTATGGTATAACTTT | 8945 |
rs549887282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101367449 | TACTAAAGTAAAATA[C/T]ATATACAAATAGTTA | 8945 |
rs549923474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498214 | GCTGGAGTGCGGTGG[C/T]GTGATCTCAGCTCAC | 8945 |
rs549926509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364369 | GCAATATCATGGTGC[A/T]ATTCTTCTATCTTTG | 8945 |
rs549941111 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101438641 | TTCATTGTAGTTTCT[A/C]CCCTTTATATGAGCC | 8945 |
rs549953840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101381200 | TTCTAGACACTATAT[A/G]TATTAACTCATTTGA | 8945 |
rs549975015 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101524593 | GTGTTAGGTGAAATT[A/G]CTTCCAAAGACTTAT | 8945 |
rs549980215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530981 | AGTTCAAGACCAGCC[C/T]GACCAACATGGTGAA | 8945 |
rs549992049 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101378423 | TTTTAATGACTGTGA[A/G]TTTTACAGTTATTTA | 8945 |
rs550002767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509068 | GATGCTCAGGTGCCA[A/G]TGGGCGCTAGCCCTT | 8945 |
rs550003241 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553788 | CTTCCCATCTACTCC[C/T]CTACGCCCCTTCAAC | 8945 |
rs550015287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521926 | TGATAAGAGAACTAG[A/G]TCTCCAGCTATATAT | 8945 |
rs550016710 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101541282 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTTT | 8945 |
rs550024542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101413373 | GGCTGGAGTGCAGTG[A/G]TGCAATCTCGGCTCA | 8945 |
rs550082046 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101530016 | TCTTAACTTCCGGAT[-/G]GAGGAATTAAATTTT | 8945 |
rs550102581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532694 | CCATCACATAATTAT[A/G]GACTACCCTGTTCCT | 8945 |
rs550129823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523880 | TCAAAATTTTTTCAT[A/G]TTATAAACCATATGA | 8945 |
rs550143625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537304 | AGACCGAGACAGGTG[A/G]ATCATTTGAGGTCAG | 8945 |
rs550147086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101477399 | AAAACTTAAGACTAA[A/G]AGGAAACATTTCTAT | 8945 |
rs550147906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418733 | TATTCTGGGGTACAT[A/G]TGCAGGATGTGCAGG | 8945 |
rs550157437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489462 | ATATTCTCCTCTCTC[A/G]TTTGACAGTTTCAAA | 8945 |
rs550161161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101472847 | ACTCCTAGATACCTA[A/T]CATCCCCTTTTTCCT | 8945 |
rs550171825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431329 | TAATCCACCCATCTC[A/G]GCTTCCCAAAGTGCT | 8945 |
rs550183789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481435 | CAATCCAAGGACAGG[G/T]TGATGATTTTAATGA | 8945 |
rs550199851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473772 | TGGCCAATTTTTTCT[A/G]TTTTTTGTAGAGACA | 8945 |
rs550215813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516267 | TAATTTGTTCCTTAC[A/C]AAAACCCAATGAAAT | 8945 |
rs550235589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101419341 | CTTTCAATCAGGAGT[C/T]TGGGCACAGCTGACC | 8945 |
rs550237450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410942 | AATTGCTTACTTTTT[A/T]AAAAAATTTTAAATG | 8945 |
rs550247211 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525247 | TACACTCCCCAAGAT[C/G]TGTTCTCCACTGTTT | 8945 |
rs550285704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527612 | TCAAAAAATTAGCTG[A/G]GCCTGGTGGCGCATG | 8945 |
rs550286309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398442 | CGAGTAGCTGGGACT[A/G]CAGGTGCCCGACACT | 8945 |
rs550293943 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101391157 | CTGTGTGGTAACTAC[C/T]GCTCCTGCTGTGATT | 8945 |
rs550353659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373794 | ATGGTGGTGGGCGCC[C/T]GTAGTCCCAGCTACT | 8945 |
rs550359092 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101446764 | TGGAATGTAAAAACT[C/T]ATTGAAGGCATATGA | 8945 |
rs550374843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439528 | ATTGGCTATGAAATA[C/T]TGAACTGTCAGAATG | 8945 |
rs550375656 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101519468 | GCTGTCAGCTGGGGG[A/C]TCCTTTCAGCAGCTA | 8945 |
rs550378870 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101543421 | CTTTATATTTAAAAT[G/T]AATTTCTCATATTCA | 8945 |
rs550379901 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101503480 | GTGCTGAAAAAACAG[A/C]TGCTGCATCTAAACT | 8945 |
rs550396204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460479 | CCCTTTCTTTGTAAT[A/G]TAGCATGCTTTTTCT | 8945 |
rs550416995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366543 | GATTTTTTAGAAGCT[C/T]TAAAGAAGAAAGTTT | 8945 |
rs550434504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101480446 | AAGTCCAAGATGAGA[A/G]CACTAGCAGATTCAG | 8945 |
rs550442812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402294 | TTATATACTTAGTAA[A/C]CCTGCTCTACAAAGC | 8945 |
rs550460549 | in-del | -/AAGGGAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101448789 | TTTTAAGAGGAAAGC[-/AAGGGAT]ATAATGTATGGTGTA | 8945 |
rs550506456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376803 | TGGTGGTGCTTTCAC[A/C]ACAACATTCTAACAC | 8945 |
rs550565618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426591 | GGGATAAATGAATGA[A/G]GAAGTGTGTTAGAAC | 8945 |
rs550569666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101369730 | TATTTTATCTTACAT[A/G]TTATTTAAAACCATG | 8945 |
rs550596728 | in-del | -/T | 0.151334 | 0.229706 | intron-variant | BTRC | GRCh38.p7 | 10:101418621 | TTTTCTCACATCTGC[-/T]TTTTTTTTTGCCAAA | 8945 |
rs550598767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477184 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 8945 |
rs550602113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392166 | TGTATTTTTGATAGC[A/G]ACTGGGTTTCACCAT | 8945 |
rs550621384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528665 | CTTCTGTTTTTACAT[A/G]TTGACTTTATTCCTG | 8945 |
rs550637998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362788 | GGTTCCATATCTGCT[A/T]ATTCAACCATTGATT | 8945 |
rs550638517 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101478250 | AGGTTGTAGTGAGCC[A/G]AGATTGTGCCACTGC | 8945 |
rs550641901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469112 | CGCAAAACTCTCTGC[C/T]TCTGGTTCAGCAATG | 8945 |
rs550660138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520234 | CTGCAACCTCTGCCT[C/G]CTGGGTTCAAGCGAT | 8945 |
rs550668236 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427406 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCTGTGTA | 8945 |
rs550676204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490776 | CTTACTATCTCTTTT[C/T]GGCTGGGTGTGGTGC | 8945 |
rs550680225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460987 | GGCTCACTGCAACCT[C/T]GGCCTCCTGGGTTCA | 8945 |
rs550688474 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101507053 | TTAATAAGATAACCA[C/T]GACATTTTAAAAGAT | 8945 |
rs550706799 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101455867 | ATTCTAATGGCCGGG[C/G]ATGGTGGCTTACGCC | 8945 |
rs550712653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502059 | GGACATATAAATAAC[C/T]TCCAAAGTTACAGGG | 8945 |
rs550721393 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101393905 | TATATTGTGGAAAAG[C/T]AGTTGAATGAGAAAA | 8945 |
rs550752806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547171 | TTCATCAGGATGTAA[C/T]CCATTGTAATTTGAG | 8945 |
rs550764089 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362307 | TCTGTAGTTTGGCTT[C/T]CCTTTCAGGGTATCT | 8945 |
rs550772663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443357 | GCAACATTAAAAGCA[A/C]ATAAATACACTGAGG | 8945 |
rs550797482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429452 | TTGTTTGTTTAGAAG[A/G]TTTTAATACCAACAG | 8945 |
rs550812728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444898 | AGTCTAACCACCCTC[C/T]CTCATTTTGTTAGGT | 8945 |
rs550814735 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101368533 | TGCCCAGGCCGGAGT[G/T]CAGTGGCATGATCAT | 8945 |
rs550815214 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101434805 | CGTCTCTACTAAAAA[A/C]GCAAATTTAGTAGAG | 8945 |
rs550816780 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101453641 | AATCAACTCTTAATT[A/T]TCCATTTTATCAGGA | 8945 |
rs550849582 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516123 | ATAGTGAAAAAGAAG[A/T]ATGTACTTTCAAAAA | 8945 |
rs550852585 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101427202 | AGCTCACTGCAACCT[A/C]CGCCTTCCGGGTTCA | 8945 |
rs550878525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484554 | TGCTATTTATAAGGC[A/G]TTTCAGCTGTTCAGA | 8945 |
rs550912958 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101513583 | ATGTTTTTGAGGTTC[A/G]TCTTTACCATTTTGT | 8945 |
rs550927886 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457015 | ATAGTTCTGAACTCC[A/G]TGTATACTATGTTTT | 8945 |
rs550986586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101378588 | GGAGTGCAGTGGCGC[A/G]ATCTTGGTGCACTGC | 8945 |
rs550998893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379213 | AAACTCTTTTCATGT[A/G]GGTATGGGTCACCTT | 8945 |
rs551011441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546236 | GGGCCATAAAAGGTA[A/C]CTTAAAAAATTTACA | 8945 |
rs551018374 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101395109 | TTCAGCTAATGTAGA[A/G]GTCATTATCACTAGG | 8945 |
rs551022004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371969 | AGAATTCTTTTTTTC[C/G]TTTTCTTTCTATAGC | 8945 |
rs551045475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482457 | TTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 8945 |
rs551047090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498866 | GGTGTAGTGGTGCGC[A/G]CCTGTAATCCCAGCT | 8945 |
rs551050172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538554 | CTTTCATCCAAAAAT[A/G]CTTTAGAGACTATAT | 8945 |
rs551135094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101490613 | GATACTTCCCCCATC[A/G]CATTGTGTAGCTTTT | 8945 |
rs551138197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539477 | GGGTCTTCCTCTGTC[A/T]CCCAGGCTATAGTGA | 8945 |
rs551153449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375270 | GCACCTTCTCTGCCC[C/G]CCTCTCTTCCCCCCT | 8945 |
rs551183551 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399033 | TCTTGGCTCACTGCA[A/G]CGTCCGCCTCCTGGG | 8945 |
rs551193621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512242 | AACCCTTGCCTATTT[C/T]ATTCTTAAATTAATT | 8945 |
rs551215450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448559 | TAAATCCTTAAGCCA[A/G]TACTACCTTAGGGTC | 8945 |
rs551258665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458025 | TTTGAAAGTTACAGA[C/T]GTAATGTTCCATCCC | 8945 |
rs551303099 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554008 | TCATATTTGCAACTC[C/T]TCTCTCTCTTTCTTC | 8945 |
rs551305493 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101362040 | ATCTCAGCTCACTGC[A/C]ACCCCCGACTCCCTG | 8945 |
rs551318418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504399 | TATATTCATTCTCCC[C/T]CTTCCCACCTATTTC | 8945 |
rs551350175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101382129 | CTGTTATTACAGGCA[C/T]CTGCCACCACGCCCG | 8945 |
rs551360770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509144 | CTCCCTGCTATCACC[A/G]TCTTCATCACTAGGT | 8945 |
rs551361789 | in-del | -/TTTG | 0.00240915 | 0.0346233 | intron-variant | BTRC | GRCh38.p7 | 10:101429431 | ACATTCTTAGGTATT[-/TTTG]TTTGTTTGTTTGTTT | 8945 |
rs551375021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101392397 | CAATCTTCAGTAAGT[A/G]ACATTTAACCATTTA | 8945 |
rs551397734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354314 | CGCCCACTGCGGGAC[C/T]GGGCAGCGGGACCCT | 8945 |
rs551402216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549953 | TAATTGGCCATGATA[A/G]GAGTTTTTAATGCCG | 8945 |
rs551404172 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446115 | TTCCCCCCCCACCCC[C/T]CCAACCCCCTCCGTG | 8945 |
rs551436475 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453709 | AGCCACTTACTAGGT[C/T]ATGGGGAATATTGCC | 8945 |
rs551439521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400362 | CAAAAGTTAAATTAA[C/G]GAGTACCCAAGAGGG | 8945 |
rs551453041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541737 | GTATATTACATTGAA[A/T]TTTTTTTAGCTTTAA | 8945 |
rs551469062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550573 | AGGTGTGAGCCACTG[C/T]GCCTGGCCTCTTTAT | 8945 |
rs551499182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533731 | GACCTAGGAAAAAAG[C/T]GGTTAAGTGCATTGT | 8945 |
rs551509663 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101410877 | TTATTATTGTCATAC[G/T]TTTTGTTTTCATGTA | 8945 |
rs551524947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473921 | TCATTTCAGATAATG[C/G]ACTTTTCAGTTCTAG | 8945 |
rs551530796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101483037 | TATTATTTATTGAAT[A/G]TGGTTCATGTAAGTT | 8945 |
rs551537032 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101368178 | CGCTCCATTAGTTCC[C/T]GCCAGAGTTGGTAGT | 8945 |
rs551544992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542432 | ATGTCAATTAAGTCA[A/G]GTTGGTTTATAATAT | 8945 |
rs551569922 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101456305 | GGGTCTGGACTAGAG[A/T]AGAAGCAGTGGAAAT | 8945 |
rs551595459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516187 | GCTCATTAAGAGTGT[C/T]GATTGACGGAACACT | 8945 |
rs551598804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360585 | CATGTTGGCCAGGCT[A/G]TTCTTGAACTCCTGA | 8945 |
rs551608298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500938 | GTGGCTCAAGTCTGT[A/G]ATCCCAGCACTTTGG | 8945 |
rs551636044 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556943 | CCCTCCTAACCCTTC[C/T]CCTTCTTGGACACTG | 8945 |
rs551638787 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101506917 | ATGGACTCAGGGTCT[C/G]TGAAAAAATTTGAGT | 8945 |
rs551659185 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546109 | TTGAATTTAGCAGTA[C/T]CATCAATCAAGTGGA | 8945 |
rs551664315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534590 | ATAAGGGGTGGAAGG[A/G]CGCATGATGGTCAAA | 8945 |
rs551665455 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | BTRC | GRCh38.p7 | 10:101517935 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8945 |
rs551677999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498402 | TCAGGTGATCTGCCC[C/G]CCTTGGCCTCCCAAA | 8945 |
rs551681453 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353879 | TCTGCGTAATGGCAA[C/T]TTATCTAAATCTGGC | 8945 |
rs551739700 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101484320 | TCAGATTATGCTGAA[A/G]CAAAATGGTCCTGGT | 8945 |
rs551749730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101513058 | TTTTGATTTTTTAAT[A/T]ATTGAACTTTTTCAT | 8945 |
rs551753941 | snp | A/G | 6.61737e-05 | 0.00575174 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521855 | TTGCAGAGAGATTTC[A/G]TAACTGCTCTGCCAG | 8945 |
rs551758864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101525842 | CTTATGGAAAAATTA[C/T]TGACACTCATTTTAC | 8945 |
rs551768324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401267 | GCAGTTTTACTCTTA[C/T]CACGTGAATGAGCAT | 8945 |
rs551768545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459260 | AGGAATAACTGTGTT[A/G]CTGAGCTTTCCTGGG | 8945 |
rs551772340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395216 | GGAAAGAAGAAGGTA[A/G]GGTTGGAGAGAGATG | 8945 |
rs551772855 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399549 | TATTCCGTGTGCCTA[A/G]CTGTTGTTGCCCCAC | 8945 |
rs551786571 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101525903 | CACACTAGGGACAAT[A/G]ATGTGCCTTCATAGC | 8945 |
rs551812768 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555531 | TGAAAAACTTGAATC[A/G]TTCACATTTCTCAGC | 8945 |
rs551816516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449973 | TTTTGTAATTGCATT[A/C]GTACATTAAGCAGGA | 8945 |
rs551842405 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101413194 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 8945 |
rs551853337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450859 | TGATAGTGGGTGCTG[C/T]ATGACGTTGTGTAAA | 8945 |
rs551856416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470853 | CAGTTGTTTCAGCAC[C/T]ATTGTTGAAAAGACT | 8945 |
rs551884085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396172 | AGTTCTTTAAAAAAA[C/T]ACACTGTCTTTGCTC | 8945 |
rs551896192 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555280 | CCAGCCTTTCTGTCA[C/T]ATGCTGCTATTACAA | 8945 |
rs551901627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101404764 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 8945 |
rs551907535 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101400833 | ACTTCTATTTGCTCT[C/T]CTTGTTATAACCAAG | 8945 |
rs551922088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357617 | AACTTTTATACAGAT[A/G]TCATGATTTCCATGG | 8945 |
rs551926529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375828 | GGTACGCCTAAAAAA[A/T]TGGCATGTTCAGCAA | 8945 |
rs551930888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371260 | ATGGCACCATCTTGG[C/T]TCACTGCAGACTCCG | 8945 |
rs551937623 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355097 | GTATCTAATAGGGTA[A/G]GCAAAACAAAATTTA | 8945 |
rs551968256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416520 | CTGGTTCATGTGACT[C/G]TTCCATGGTGTCAAT | 8945 |
rs551990945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425243 | CTTTACTATCGCATT[G/T]CAGCATTTCAATTTT | 8945 |
rs551994776 | in-del | -/AAAG | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101510156 | AAAAAAAGAAAAGAA[-/AAAG]AAAGATGCTTTTACA | 8945 |
rs552014705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101364169 | TTTCTTCTTTCTGCT[C/G]TCTATTGTTGACACT | 8945 |
rs552047631 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101492234 | AGAAATTTAATTATA[C/G]AGTTTTGGGTTTGTT | 8945 |
rs552054784 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101477372 | TGATAAACATAATTT[A/G]TACCATCAGTAAAAA | 8945 |
rs552065962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520989 | AAAGTTGTGATGACG[A/G]AGCACAATAGCTCAC | 8945 |
rs552082374 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101467333 | AGGCAGGCAGGGTTT[G/T]TTTTTTTTTTTTCTC | 8945 |
rs552134286 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101520967 | ACTGTCTCCAAAAAC[-/A]AAAAAAAAAGTTGTG | 8945 |
rs552139028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422923 | CTCCAGCTTTGTTCT[C/T]TTGGCTTAGGATTGA | 8945 |
rs552166096 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101366162 | AATTGTGCTGGAGTA[A/C]CACATTTTCTGTTAA | 8945 |
rs552172983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461753 | ACACAATGCTTAAAG[A/T]TACATGAAATACTTC | 8945 |
rs552199914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101530818 | CCTCCGCAGACAGCT[A/G]TGGAGAGTATATGGA | 8945 |
rs552224994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423842 | AAATAAATGGCTTCC[C/T]AGAACAGTTTGAAAT | 8945 |
rs552297058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454656 | GTGTAGTGGCGTATA[C/G]CTGTAGTCTTAGCTA | 8945 |
rs552345403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388760 | CCTCTCAAAGTGCTG[A/G]GATTACAGGCATGAG | 8945 |
rs552357603 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101389351 | CTTTGGGTTATTATC[A/C]TTTCTTTTATGGAAA | 8945 |
rs552361109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532622 | ACTATACAAACGGGT[A/G]GTCCTAGGGTTAAAT | 8945 |
rs552374014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547397 | GGCTGGAGTAGTGCA[A/G]TGGCGCAATCTCGGC | 8945 |
rs552383573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472786 | TTATTCGCTTGTCTC[A/C]TAGCCTTCATTTTTT | 8945 |
rs552384753 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101428841 | ATCTATCTATCTTTA[A/T]TTAGATAAGAGACGG | 8945 |
rs552393398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101478193 | GTAAGCCCAGCTACT[C/T]GGGAGACTCAGGTGG | 8945 |
rs552398058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523665 | ATATTTTGGCAGGTA[A/G]CCTGTTTTCTCTACG | 8945 |
rs552415190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429703 | ATACCCCCCACCCCC[C/T]ACAGACCCCAATCCA | 8945 |
rs552419312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548268 | ATTCAGCAAAAGACA[C/T]GTACATAAATGTTCC | 8945 |
rs552420465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464399 | TAAAAATAAATGCAT[A/T]CATTATTGAATCATT | 8945 |
rs552429851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470263 | TCTATGGTTTGCCTG[C/T]TTATGGTATGTTTTG | 8945 |
rs552471649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420448 | ACTGCTGGACCACTG[C/T]CTCTCCCTCTCTTAA | 8945 |
rs552473611 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461865 | ATCTTCAAGTGAATA[A/G]TTGTATAAATATATG | 8945 |
rs552485459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412710 | CATAGTATATTAACT[A/G]TGAGTAACTATGTAA | 8945 |
rs552509524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465736 | AATGAAGGTGGAAAT[G/T]AAGAGACACTGTTCC | 8945 |
rs552517070 | in-del | -/GGCT | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101409828 | TGATAAGTATTTTTG[-/GGCT]GTTTTCAACCTTTTG | 8945 |
rs552526258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531852 | GAGTTAAAGAGATTG[A/G]TCCCTTCATACATAG | 8945 |
rs552557839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438318 | TAGTCCCAGCTCCTC[A/G]GGAGGCTGAGGCAGG | 8945 |
rs552559945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101381157 | TAATGGCAGCCAACA[C/T]TTGTAGCTCAGTATA | 8945 |
rs552604242 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433817 | AAAGGATAATTTCAG[C/T]AGTTGAAGAGAGAGA | 8945 |
rs552609858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481284 | GTGCATGGAAACAGG[G/T]ATACACAGTTATTTG | 8945 |
rs552624072 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101480894 | CAACTAACAAGTGCT[A/G]ATTGACCCTATTTTA | 8945 |
rs552628406 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495542 | AGGGAGCTCTAACCT[A/T]GTTCAGAGTGGTGGC | 8945 |
rs552641842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366411 | TTTATAAATATCTCT[C/T]AAGGCGCACTTTGTT | 8945 |
rs552655947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367210 | CCAGTGGCTGGGACT[A/G]CATGCGCGCACCACC | 8945 |
rs552674459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522913 | AACAGAATATTTAAA[G/T]TCTACAGATGGGTTG | 8945 |
rs552679359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406270 | CAAGCTCCGCCTCCC[A/G]GGTTCATGCCATTCT | 8945 |
rs552680355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360895 | CCTGCAGCCTCAAAC[A/T]CCTGGGCTGAAGCAA | 8945 |
rs552691729 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498722 | CAGGCCAGCCGTGGT[A/G]GTTCACGCCTGTATT | 8945 |
rs552697769 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101378226 | GTCTGTATTATAAGA[A/G]GCAAACTTAAATGAT | 8945 |
rs552722579 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101443622 | GTTTTAATTTCTTCT[A/G/T]TGTAATCTTCATTAT | 8945 |
rs552731336 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353500 | GTGGGGGAGAAAAGA[G/T]TCCTCGGGAGAAGTG | 8945 |
rs552738936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380393 | TTTTTTTTTTAATTA[A/G]AAAGTAAACTTTAAT | 8945 |
rs552759570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438057 | GGAGTATTCATTTTC[A/G]TACTTGATTCTTTAA | 8945 |
rs552798450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372778 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 8945 |
rs552800757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509543 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTTTTT | 8945 |
rs552808162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424830 | TTATTTTAAAATTGG[A/G]GTATATGTGCAGGTT | 8945 |
rs552817244 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101546805 | CAGACTATGAAAAAC[-/AAAG]AAGACATAATGTACT | 8945 |
rs552838105 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423899 | CCTGGTGATGATGCC[A/G]TTTATATTTTTTTCT | 8945 |
rs552850272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486996 | TAGTAATCAATCTTA[C/T]TGAAACATTACATTT | 8945 |
rs552858461 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101528498 | ACAGAAACCCATTCC[C/T]GCTCTTTTGAGTATC | 8945 |
rs552889773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474669 | TGGCAGTTTTGAACT[C/G]TTATCACTTGATATC | 8945 |
rs552894434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425464 | AACTAATATGTGCTG[C/T]GCAGGGCTGGATTTG | 8945 |
rs552913245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541881 | CTGTGTTTGTAAGGG[A/T]TATTGGTTTGTTGCT | 8945 |
rs552921727 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526349 | TAACAGAGAACAAAT[A/G]TTCATATACTCAGCA | 8945 |
rs552924156 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101445174 | GACTCTCTGGTAAGA[G/T]CTTTCTGATTTCTTA | 8945 |
rs552935766 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101482552 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 8945 |
rs552945202 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398332 | TTGTTTTTTTGAGAC[A/G]GACTCTTGCTCTGTC | 8945 |
rs552953319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101369897 | CTTTCTATGTGACCA[C/T]TCTCATGTTGCTGCT | 8945 |
rs552969467 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543812 | TTTTTCACCCCCATC[C/T]TTTATGCTATTGTTG | 8945 |
rs552975061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101354788 | AATGAGGAGGGAGGA[C/T]AGCCTTTGCCTTGAG | 8945 |
rs552983687 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101354037 | ACGGAGAAGCCGATT[C/G]TCCTTGGCCCCTCAG | 8945 |
rs552991186 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526182 | TCTGTGGAGAGGCCT[C/G]GCAGAACGAAGAGGA | 8945 |
rs552994455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484721 | GATATAACCACGTCA[C/T]TGAGGCTGATGTGGT | 8945 |
rs553011698 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101359781 | AATTTTGTATTTTTG[A/G]TAGAGACAGGGCTTT | 8945 |
rs553061051 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482734 | CTTGACCTTTGAATG[C/G]AATGACTTGTCATTA | 8945 |
rs553065203 | in-del | -/A | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101513996 | TCATAATGTCTTGAT[-/A]TTTTAATTTGCATTT | 8945 |
rs553099274 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424873 | ATACTGCACGATGCT[G/T]AGGTTTGGAGTCTGA | 8945 |
rs553112186 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101376299 | CACTGCACTCCAGCA[C/T]GTGTGACAGAGCAAG | 8945 |
rs553113656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536155 | GTGGCAGAGGGGGAG[C/G]TGCTTTGTGAGAACA | 8945 |
rs553114505 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454430 | AGAATGTGTAAGACT[G/T]GAATAGATGAGATAA | 8945 |
rs553115903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518587 | GAGTTGCTGGGGCCA[A/G]TCTGTGGAGATTAGT | 8945 |
rs553117394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434919 | GGATTACTGGCATGA[C/G]CCACTGCACCTGGCC | 8945 |
rs553122842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383481 | GCAGATATTTTGCTC[A/G]TGATTATTTGGACCG | 8945 |
rs553123103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459743 | TGTGTTTTCATTCTT[C/T]AGACATTTTCATAAT | 8945 |
rs553144839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400897 | TCCCTCCTTTTTTCC[A/G]TCCCCACTATCCTCC | 8945 |
rs553152466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418300 | TTGAACCTGAGAGGC[A/G]GAGGTTGCAGTGAGC | 8945 |
rs553161067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490817 | TAATCCCAGCACTTT[A/G]GGAGGCCTAGGTGGG | 8945 |
rs553173276 | in-del | -/AAA | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101382489 | TGATTAGATCAGGGT[-/AAA]AAATTTGGCAGGAGT | 8945 |
rs553187589 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488122 | TACATTTTTTAAAGT[G/T]CTGCCTTGTCAGCCT | 8945 |
rs553192137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542624 | CCGCCCAGGCTGGAA[C/T]GCAGTGGCACACCCA | 8945 |
rs553193713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374964 | GATCTGCCAGTTAAG[A/G]AGGCACAAAGCTACA | 8945 |
rs553202207 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101422754 | TTCTTGTTTTTGTCA[C/G]GTTTGTCAAAGATCA | 8945 |
rs553212030 | in-del | -/ACGTT | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101358403 | CCACCTTGCCAAGCC[-/ACGTT]TATTTTTAAAAACAG | 8945 |
rs553216633 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101417633 | GAGGTATTTTGAGAC[-/TATT]TAAGTATCCTCCTCC | 8945 |
rs553218687 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396951 | GGGATTACAGGCATC[C/T]GCCACCTCGCCTGGC | 8945 |
rs553270544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101493103 | AAATGTGTAGTAAAG[C/G]TTATTTATAAAAGAC | 8945 |
rs553277606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368335 | TGCTAGCACCATGCT[G/T]CTTGTACAGCCTGCA | 8945 |
rs553280194 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534734 | GTTCTGCACTTGCGT[C/T]TCAATAATGGCATGA | 8945 |
rs553282043 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352201 | TTTTCATACGAATGC[A/G]TTTGAAGTCTTCTCC | 8945 |
rs553303768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384363 | GCAGCTATTTCTTTC[C/T]GAATAAAAAGTTTAA | 8945 |
rs553345899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101497741 | AAATAAACGAAGTTG[A/G]CTGGGCGTGATGACT | 8945 |
rs553345942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487375 | GTGGGTATTACCACA[A/G]TAAATACTTACTTGC | 8945 |
rs553362351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373120 | AAATTTAATCCTCTT[C/T]GTTGCTGATAGTGCA | 8945 |
rs553390632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536864 | TTATTATACTTGTTT[G/T]CACATGGTTGTCATT | 8945 |
rs553394296 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541496 | CGATCTCCTGACCTC[G/T]TGATCCAGCCACCTC | 8945 |
rs553401097 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101496040 | GTCTGAATTATTTCA[C/G]TGTTTTTGAGAGTCA | 8945 |
rs553401264 | in-del | -/TGATT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101435388 | ATGCAATTACTGTTC[-/TGATT]TGTCACCAAGAATTT | 8945 |
rs553410319 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101519650 | ATGACAGCAATACCT[A/C]CATTACTGTTTGAAT | 8945 |
rs553412910 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101476615 | AGGCCTGTGCTGCCA[C/T]GCCCAGTTAATTTTT | 8945 |
rs553413470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531445 | TGACATGAGTTGGGA[A/G]TCAATCTCTTAGCTG | 8945 |
rs553424194 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101544564 | GCTTGTGCCACCATA[A/T]CTGGCTAATTTTCTT | 8945 |
rs553425813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365673 | TTAGAGACAGGGTTT[C/T]ACCATGTTGGCCAGG | 8945 |
rs553427199 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549981 | CCGTGGAAATCTACC[A/G]ATGGTTTTACAAAGT | 8945 |
rs553486036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380753 | AGAAGAACTGGTTTC[A/C]AGTCCTGTCTTAACT | 8945 |
rs553497456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101532190 | CCCTAAGTTGTGTAT[A/G]TCCCATAGAGTAAAG | 8945 |
rs553525679 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101462916 | TCTGTCGCCCAGGCT[G/T]GAGTGCAGTGGCGTG | 8945 |
rs553559141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392581 | CTTGGCTCACTGCAA[C/G]CTCCGCCTCCCAGGT | 8945 |
rs553606430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101480531 | TCACATGATAGAAGA[C/G]ACTAGCTAGATATCC | 8945 |
rs553622453 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101393327 | TCTGTGAGCCACTTC[A/C]GCAAATTAATTGAAC | 8945 |
rs553627146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443006 | CCTGCCTCAGCCTCT[C/T]GAGTAGCTGGGACTA | 8945 |
rs553656960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101496892 | AAACTGTGACTTGCC[G/T]TTTCACTTTTTAAAT | 8945 |
rs553683476 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365080 | ATTTTTTTATTTTTA[-/T]TTTTTTTTTTAAGAT | 8945 |
rs553693664 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101405163 | TGGTTCCCTGGGGCC[A/G]CCTTTTTCAGTCCTC | 8945 |
rs553704267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398572 | CCTCCCAAAGTGCTG[A/G]GATTATAGGCATGAG | 8945 |
rs553715892 | in-del | -/GTG | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101464876 | TTGTGTCTGTCTATT[-/GTG]GTGGTCACTCCCTAG | 8945 |
rs553735892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543869 | ATCATCCCCACAGCA[C/T]TTGTTATTTTTGCTT | 8945 |
rs553750661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101505719 | ATTATGGGCAATTTC[C/T]ATGTTTTTTGTGTAT | 8945 |
rs553751816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539855 | GCACAGTCTGTAATT[C/T]AGTCATTCTCATTGT | 8945 |
rs553762096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479747 | TTTGTATAAGATAAT[A/G]TACAATTGTTTTGAT | 8945 |
rs553788569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422279 | GTCTTCTTCTGAGAA[A/G]TGTCTGTTCATATCC | 8945 |
rs553815994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389036 | CTAATAGTCTCTAAC[C/T]CATCCTTTTACTGTG | 8945 |
rs553823817 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101429900 | CTTAACTGTGGTGTT[C/T]TGTTTTCTAATTTAC | 8945 |
rs553828712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101549525 | CAAGACCATCCTGGC[C/T]AACACGATGAAACCC | 8945 |
rs553850079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471662 | ATAATCCTGGTGGTG[G/T]TTCTTCCTTCAGATT | 8945 |
rs553862555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101430801 | ATAAAGCCAATTAGT[A/G]TAATCAATCAATTAA | 8945 |
rs553891121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448783 | TTACCATTTTAAGAG[G/T]AAAGCAAGGGATATA | 8945 |
rs553933059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523069 | ATTAGCTGGGTGTAG[G/T]AGCACACACCTGTTA | 8945 |
rs553933200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366674 | AAGTTGGGCAGGTGC[A/G]GTGAGTTATAGGTGG | 8945 |
rs553938911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446052 | CTTATTGGATGAAAG[A/G]CATTCAGCCTGGAGA | 8945 |
rs553972669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440425 | AAAAGAGTTTGTATT[C/G]AAAGTTCCTCAATGG | 8945 |
rs553994816 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499379 | TAGGCATGCACCACC[A/G]TGCCCAGCTAAATTT | 8945 |
rs554001302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101382293 | CGGCCCCTAAGAATG[C/T]CTTTTACAGCTCTTT | 8945 |
rs554024678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406608 | GGTGTGATCTTGGCT[C/T]ACTGCACCTCCACCT | 8945 |
rs554029824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472510 | ATTTTTTTCCTTTCA[A/G]CACTTTAAAAATATT | 8945 |
rs554030229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101396429 | TTTTTTTTTTTTGGT[A/G]GAGACATGGTCTCAC | 8945 |
rs554070182 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101547568 | CTGGTCTCAAACTCC[A/G]GACCTCATGATCCAC | 8945 |
rs554100373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402436 | ACTTAATAAATAATG[A/G]ATATAATTTATTTTA | 8945 |
rs554103261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437725 | TTTGAATTTGGCTTA[C/T]ATCTGACCACCACCT | 8945 |
rs554106999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101470511 | ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 8945 |
rs554142911 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411633 | TGGAACTTTTTATTT[C/T]ATTCTTTTTTTATAC | 8945 |
rs554169583 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518938 | TTATTAATTCTGTGT[C/G]TAGTTCTGAGGGTCA | 8945 |
rs554172115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508310 | AAGCTTTTTCTTGTT[A/G]GTTATTAGAAATCAT | 8945 |
rs554173951 | in-del | -/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352722 | TAACTCACTTTTTTT[-/T]TTTTTTTTTTTTTAG | 8945 |
rs554194943 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101501972 | CTCAAAATTCTATGT[A/C]TTTTCTCAGAAAGAC | 8945 |
rs554220903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552541 | TTCTTAGGCTGCCTT[C/T]TCTATTCCCAAGGCT | 8945 |
rs554262104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499082 | TATTTCATATACATA[A/C]TCTGTTATTTCATAT | 8945 |
rs554270318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391601 | AATGGCAATGTTGAC[A/G]TGTACCTTAATTTGC | 8945 |
rs554276346 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101541465 | CGGGGTTTCATCATG[G/T]TAGCCAGGATGGTCT | 8945 |
rs554318057 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502639 | TATAGTGATAGTAGC[A/G]TCCTTCTTGGTGAGA | 8945 |
rs554322699 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460387 | CCTTCCTCCATTTTT[A/T]GGTAGATGATCTCCA | 8945 |
rs554328083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490278 | TCCTTTCTTCTTCCT[C/T]CCTTCCTTTTCAGTT | 8945 |
rs554404061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544722 | GGCTCTGAAAAAGTT[G/T]TCGTTTTGCCTTCAT | 8945 |
rs554452943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463943 | TTGAATCATCCAGGA[A/C]GCTTTAAAAAAAAAA | 8945 |
rs554453216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361984 | TCTTCCCCCTTGAGA[C/T]GGAGTCTCACTCTGT | 8945 |
rs554456763 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101470950 | TCTCAAACCTCCTGA[A/G]GAAAACGTTGCTGCT | 8945 |
rs554462532 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352468 | AGTTTTTGGGGTACA[A/C]GTGGTTTTTGGTTAT | 8945 |
rs554488371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401790 | CTGCAGTGAGCTATG[A/G]TTATGCCACTGCACT | 8945 |
rs554526911 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101362916 | TTACATTGCATTATT[A/T]TATGTAATCTAGAGA | 8945 |
rs554529817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511440 | TTTTAAACATGATCT[C/T]ACTCTGTTGCCCAGG | 8945 |
rs554560639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452211 | TGCACTATGACAATT[A/T]ATCAGTTTCTGCATA | 8945 |
rs554565524 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101430187 | TTTGGGATTCTCTCT[C/G]GGGTTAAAGCCAGTA | 8945 |
rs554579113 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101489191 | TTAGACTTGTATGTA[C/T]CAATATTTTAGAATC | 8945 |
rs554608642 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101510376 | TTAGCCGAGCGTGGT[C/G]GTGGGTGCCTGTAGT | 8945 |
rs554626968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478321 | AAAAAAAAATAGGTA[A/G]GTGTTGGTTTATCTT | 8945 |
rs554636381 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101412582 | TAATTTTATTTAAAC[-/TT]AATGTACTAGAAGTC | 8945 |
rs554644402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444194 | TTCTCTTGCCTTTAC[A/G]TACCTTCTAAGGGAA | 8945 |
rs554647234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420874 | TTTTGAAAAACTCAC[C/T]GGTATTTTTACAACA | 8945 |
rs554708072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475427 | TGTCTGTAATCCCAG[A/C]TACTTGGTAGGCTGA | 8945 |
rs554714259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364517 | GCTTTCCATCTCTTC[C/G]CTGCACCTAAACTTA | 8945 |
rs554730318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418145 | GCCGAGGCAGGTGGG[G/T]CATTTGAGGCCAGGA | 8945 |
rs554747071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412902 | TTTATAGAAATAGAT[A/C]ATCAAAAGTGGAAAT | 8945 |
rs554762739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436225 | GCAAATGGTGATCCT[A/T]TAATCTATAATATTA | 8945 |
rs554784388 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402553 | TTTAGTCCAAGTTTC[G/T]TGGAGAAAATAATTC | 8945 |
rs554793854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362289 | TCTAAAGTCTTGCTC[C/T]TTTCTGTAGTTTGGC | 8945 |
rs554799254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428340 | AGTAGATATCTCATC[A/G]TGAATTATTGATGAG | 8945 |
rs554852003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467689 | CTAAAGTGCTTTGGG[C/T]TTTGGGTAAAAAAAA | 8945 |
rs554853772 | in-del | -/C | 0.046775 | 0.145601 | intron-variant | BTRC | GRCh38.p7 | 10:101446101 | ACATTTTGTTCTCTT[-/C]CCCCCCCCACCCCCC | 8945 |
rs554855708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484996 | AGAATACATTTTCTT[C/T]TAGATGTGCGTGCCG | 8945 |
rs554859465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101387325 | ATTTTTTTTTGTATT[A/G]GGAACATTCAATATT | 8945 |
rs554860933 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101410169 | AGCTTCTTCTAGTAC[A/G]TCTGGATTTCCTGGT | 8945 |
rs554870536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404751 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 8945 |
rs554888665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468573 | TCCTTAGATATTGCT[G/T]TTTGGTTTGCTTTTT | 8945 |
rs554889044 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101429026 | ATATTTTGTTTCCCA[A/G]TATTACTTTCTACAA | 8945 |
rs554900877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101371822 | TGGTGTGAGGTAGAC[A/G]TCAGCATTCTTTTTT | 8945 |
rs554902939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101473203 | ATGATTTCAGTTTAT[C/T]TATCTTTTTTTTTTT | 8945 |
rs554917226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412138 | GTTTTTTGCCTAGTG[C/T]TGTGGAATTTCACTG | 8945 |
rs554923865 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101411318 | ACTTTTTATAGTTTT[C/G]TATGGGTTGGTCTAT | 8945 |
rs554933624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101363870 | AATTACCGATGAAGT[A/G]CAGTAAGACTCTACT | 8945 |
rs554945058 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101431910 | ACAATATAGTAAAGC[A/C]TGCAGGTTCTAAAAT | 8945 |
rs554951420 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101401923 | GGAAAAAAGAAAAAC[-/AG]AATGTTGATGTTAGA | 8945 |
rs554979737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486301 | TCGGCAAGAGTCCGC[A/T]TAAATCTGCCCGAAT | 8945 |
rs554982623 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101481577 | TTTTTTTTTTAATTG[-/T]TTTTTTTCTCCCACC | 8945 |
rs554986388 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101408166 | CAAGTGCTCAGTAGC[C/T]GTATGTGACTAGTGG | 8945 |
rs554989137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101530077 | GATTTTTTTTTTGTA[C/G]CAAAGATCTAGCTTG | 8945 |
rs554992546 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101474011 | TTCATTGTGATCATA[A/T]CTTTTATTGCTATGT | 8945 |
rs554994382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464950 | GGGGTCAATAGAAGC[A/G]GGTCACAGGGCAGCT | 8945 |
rs555011576 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380767 | CAAGTCCTGTCTTAA[C/G]TACAGTCATGCATTG | 8945 |
rs555012348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101538769 | AAGTGCCCTGGGGGC[C/T]GGGTGCGGTGGCTCA | 8945 |
rs555048085 | in-del | -/TTTGG | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101511545 | TTTGTATTTTGGGTT[-/TTTGG]TTTTGTTTTGTTTTG | 8945 |
rs555051944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101367793 | TGTGGTGTGTTTATT[C/T]TTGTTAATGTATTCC | 8945 |
rs555054434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101513519 | TCCTAGAGTTTCATA[C/T]GAGTAGAATCATAAT | 8945 |
rs555073216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521250 | CTGCACTCCAGCCTG[A/G]GTGACAGAGTGAGAC | 8945 |
rs555081284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403662 | GTAGCATGATCATGG[C/G]TCACTGCAGCCTCGA | 8945 |
rs555089664 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101526582 | GCCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACGT | 8945 |
rs555140769 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101522106 | GGTGTGATCTCAGCT[C/G]ACTGCAACACTGCAA | 8945 |
rs555147114 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101384137 | TTCAGTATTTAAGTA[A/T]TCTCTGTTATACTTT | 8945 |
rs555174748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485571 | TTTACAAATCTAAAA[C/T]TTTCGGTAGTTCTTT | 8945 |
rs555196948 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364238 | ACCTGTTGATTGGAT[A/G]CTCCTAGAATCATAA | 8945 |
rs555207355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537907 | GAAGAGCTACACTTA[C/T]CTTATTTAAATCAAA | 8945 |
rs555212237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378769 | ACCTCAAGTGATCCG[C/T]CCACTTCGGCCTCCC | 8945 |
rs555214139 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101370861 | CTGGGGTTACAGGTG[C/T]GCACCACTTCACTGG | 8945 |
rs555264824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101477674 | TTTTATTTGGAGACA[A/G]TGTCTTGCTCTGTTG | 8945 |
rs555289131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101419811 | TCTCAAATGTAGCCT[G/T]CCTCAGTCTTTCACT | 8945 |
rs555296445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549478 | CCAGCACTTTGGGAG[A/G]CCGAGGCGGGTGGAT | 8945 |
rs555300567 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101489952 | GTCACCTTAAAGTCT[A/T]CTAATTCCAATTAAG | 8945 |
rs555308553 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530441 | CAAAAGTGATCTCCA[A/T]GCCAGAGGCATTGCT | 8945 |
rs555325754 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101478190 | CCTGTAAGCCCAGCT[A/G]CTCGGGAGACTCAGG | 8945 |
rs555329249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431861 | TTCCTTTACAAAATT[G/T]AATATTAAACTTCCT | 8945 |
rs555341809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384276 | TTGAGTCTCCTATTA[G/T]AAATACTATAAACAT | 8945 |
rs555349270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529199 | CATCATAAAAGGTTT[C/T]GACTTAAAACATAAA | 8945 |
rs555354827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101360254 | GAGACAGGGTTTCAC[C/T]GTGTTGCCCGGGCTG | 8945 |
rs555356813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101524267 | TGTTTTAGCCATAGG[C/G]AAATAGTTTTCTTTG | 8945 |
rs555381490 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101439107 | ATTTGATTGACAAGT[A/C]AGAAATGCATTAGAT | 8945 |
rs555385370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101368271 | CATGCAGCTCCTCTT[C/T]GCCCTCCACCGTGAG | 8945 |
rs555387088 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101475241 | TTTTTAAGGTTTAGC[C/G]TGTTTAAAAGAAAAA | 8945 |
rs555388535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482046 | TTTTTGTGAGATGGA[G/T]TCTCACTTTGTCACC | 8945 |
rs555388955 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101420641 | CCCCCTCCCAGCAGA[-/T]TTTTTTCCTATCACT | 8945 |
rs555411325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376875 | TTCCACTCTCATTCC[A/G]TTTTACTCTTTAAAT | 8945 |
rs555416598 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101411082 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 8945 |
rs555416747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101533806 | GTGAATAGAAAAGAC[A/G]GTTCCTGTTTTTTGT | 8945 |
rs555417196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424163 | CACTTGAACCTGGGA[G/T]GCGGAGGTTGCAGTG | 8945 |
rs555459903 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442914 | TTTTTTTTTTTGAGA[C/G]GGAGTCTCGCTCTGT | 8945 |
rs555467213 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535993 | TACTGTTTGTTATAT[C/G/T]TAAGGAAATTATTCC | 8945 |
rs555468224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492072 | CATAAAGTATGTAAG[A/G]AACACTTGCTCAACA | 8945 |
rs555484052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407475 | CTGGAGTGAAGTGGC[A/G]TGATCTTGGCTCACT | 8945 |
rs555502784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542792 | ATTGCCCAGGCTGGT[C/T]TGGAACTCCTGGGCT | 8945 |
rs555506810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101483382 | GGTGGATCACGAGGT[C/T]AGGAGTTCAAGACCA | 8945 |
rs555534000 | in-del | -/TTG | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353029 | GGCCCTAAATCACTT[-/TTG]TTGTTGTTGTTGTTG | 8945 |
rs555536292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101390893 | GTGCATCAGTTAAGA[C/T]AGATTAATTTTATAC | 8945 |
rs555608219 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101374178 | GTTTACAGTCCCACC[A/C]ACAGTGTAAAAGTGT | 8945 |
rs555608225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101382198 | ATGCTGGCCAGGCTG[A/G]TCTCGAACTCCCGAC | 8945 |
rs555623763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417373 | CCAGTATCTTGCAGA[A/C]CATTTTTCAAATTGG | 8945 |
rs555645452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500161 | TTTTGTTGTATTGCA[A/G]ACATTATAGAGTGTA | 8945 |
rs555654012 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101458277 | TCAAAGGTTACGTAC[A/G]ATATAATTCCATTTA | 8945 |
rs555689279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541421 | CGTGCCACCATGCCC[A/G]GCTGATTTTTTGTAT | 8945 |
rs555691082 | in-del | -/AAA | 0.484279 | 0.0872533 | intron-variant | BTRC | GRCh38.p7 | 10:101438422 | GAGCGAGACTGCCTC[-/AAA]AAAAAAAAAAAAAAA | 8945 |
rs555692578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449514 | GATCTCTGGATGAAA[C/T]ATTTTTGTAAATATG | 8945 |
rs555702834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391783 | TATATTAAGGCACAA[G/T]ATATACACTTAGGGT | 8945 |
rs555724329 | snp | A/G | 3.3145e-05 | 0.0040708 | intron-variant | BTRC | GRCh38.p7 | 10:101532905 | CAACAAGTCTCCACA[A/G]CACCCCATCATCACA | 8945 |
rs555738116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387985 | GTGAGCCACCATGCC[C/T]GGCCTTTGGAAATTT | 8945 |
rs555755631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551721 | AGTGTTCCGCTGAGG[A/G]CAGTGATTCACGCCC | 8945 |
rs555780801 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432650 | CACAACCACTCTTAG[G/T]TTTGATAACTTGCTA | 8945 |
rs555796794 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101543034 | GGCACCTGCCACCAC[A/C]CCTGGCTAATTTTTT | 8945 |
rs555803548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407693 | CTGTGCCCAGCCTAA[C/T]ACAGTGTAGTTTAAA | 8945 |
rs555818299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433767 | ATTACTCTGGCTATA[A/G]GAAGATGCATTTAGA | 8945 |
rs555818665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101543705 | GGGACCTAGGGTTTA[C/T]AATAGTTATCTCTAA | 8945 |
rs555823525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550933 | ACTGTGGGTAGGAGA[C/T]GGGATATTAGCTGTA | 8945 |
rs555830221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101539099 | GAATCCCCCTGGTCA[A/G]CCCCTTAGTTCTGCA | 8945 |
rs555845658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483902 | GGCTGAAAAGCATTA[C/G]TTTTTTATGTTATCT | 8945 |
rs555851186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434469 | CCTAAATCGGAGTTA[A/C]CATGTATAAAACTAA | 8945 |
rs555866884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101539783 | TTTACCCTTTTACAT[C/T]ATAGTATATAGCAGT | 8945 |
rs555872344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426665 | ATAACGCAGATTTTT[A/T]TGTAAAACGGAGGAG | 8945 |
rs555904899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518005 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 8945 |
rs555908668 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555366 | TCAGTTGAAGGAATA[C/T]TGTTTCTAAGACTGT | 8945 |
rs555918452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474784 | CATAAACACACATCT[C/T]ACCCAGTGTGGTTCT | 8945 |
rs555920028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356383 | TAAAGAGACATTATG[A/C]GATCATCCTTTTTAC | 8945 |
rs555935594 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101416886 | GCATGAAATTTAGTC[C/T]GATAATAATTACTAC | 8945 |
rs555998499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487119 | ATTTGTTGTTATATG[G/T]GACAAAATAAAATCA | 8945 |
rs556003841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101513255 | TATTACAGTGGATTT[A/G]TCAGTAGGAATACTG | 8945 |
rs556021850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450037 | GTAAGGTAGGAAGTG[G/T]TTTTTTTTGTTTGTT | 8945 |
rs556032387 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101529913 | GGCATTTCTGCCTCT[C/T]TCCACTTTGCAAGGC | 8945 |
rs556057003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101392469 | ATTATTTTTTAAACT[A/G]AAAATTAATTGAAAG | 8945 |
rs556063752 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392384 | GTTGTGGAATTCCCA[A/G]TCTTCAGTAAGTGAC | 8945 |
rs556071846 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452474 | AGGATTAAGAATTTG[A/G]AAGCATAAAAAATAG | 8945 |
rs556074741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387590 | GGAGTGCAATGGTGC[A/G]ATCTTGGCTCACTGC | 8945 |
rs556084588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461807 | ATTTATATACATGGG[C/T]ATATGTTTTCTTTTA | 8945 |
rs556084616 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377178 | GTTACTGACCTCTTC[C/T]GTTCAGCATAATGCC | 8945 |
rs556085435 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554345 | TGAATACCCAGGTGC[A/C]TGTATCTTTGCCAAG | 8945 |
rs556091891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441130 | TCATTGGCTGATTTC[C/T]ACAGGATGAATGAAA | 8945 |
rs556099198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406459 | GTGAGCCACTGCACC[C/T]GGCCTACTGCTTATA | 8945 |
rs556119041 | in-del | -/T/TTCTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101472324 | TTCTCTTCTCTTCTC[-/T/TTCTA]TCTCTTCTTTCTTTC | 8945 |
rs556126404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546839 | AATATCAGAAATGAA[A/G]GAGATCCCAGATCTT | 8945 |
rs556129127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441940 | AGACACGTCTTGTTT[G/T]GAACACAATTTAAAT | 8945 |
rs556150849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486547 | AAACAGGAGGAAGCC[A/G]TGTTTCCTCCTAATA | 8945 |
rs556172564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101453927 | CTCTTCCGTTGTAGT[A/G]TGAAAGCAGCCACAG | 8945 |
rs556195796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101372190 | TCTGATAGTATATGC[C/T]CCTCAGCTTCCCCTT | 8945 |
rs556214530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101437458 | TGGTTTCATTTTTAA[A/G]TATTTTATTACATTT | 8945 |
rs556219462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395261 | ATTTCAACCCATTCC[A/G]TTGGTTTAATTTTCG | 8945 |
rs556248156 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101463917 | TAAAAATAATTGTTT[A/C]GTAAATAGAATTGAA | 8945 |
rs556249037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438165 | TATAAGTCTTCTCAC[A/G]TCTGTAATCCCAGCA | 8945 |
rs556268806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448642 | TTTCTGTTTAAAAAC[A/G]TATTTTCTCTCATTC | 8945 |
rs556268817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439237 | GGAAACACAAATTGG[A/G]TGTGTGCCTGAGCGC | 8945 |
rs556286637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101456110 | CAGGAGGCAGAAGTT[A/G]TAATGAGCCGAGGTC | 8945 |
rs556290170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461269 | GAAAATGGAACTCAA[A/T]TAATATGTAATTTGG | 8945 |
rs556307239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101397294 | GGGAAAATGAAAACA[A/G]CCCAGATAAGCTGCA | 8945 |
rs556313402 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101502679 | TCCAAATATGTTTAC[A/G]CCACAAGACATTTTA | 8945 |
rs556318043 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101508936 | AAAAAAAAAAAAAAA[-/A]CTAAAAGTAGAATGT | 8945 |
rs556347652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394752 | CCTGCAGTTCCCTGT[A/G]GAGTAGTACATGGCT | 8945 |
rs556351616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494942 | AAAGTGTCAGTGGTA[A/G]AGGGAGTTTACAAGC | 8945 |
rs556352720 | snp | A/G | 1.66985e-05 | 0.00288946 | intron-variant | BTRC | GRCh38.p7 | 10:101531344 | TTGAGGTAAGAATCT[A/G]TGTATTTTGGGGTAT | 8945 |
rs556370587 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461808 | TTTATATACATGGGC[A/G]TATGTTTTCTTTTAC | 8945 |
rs556394138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532018 | GTAGTTCGTAGCTTT[C/T]CTTCTCTTGATGAGT | 8945 |
rs556395071 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471909 | ATCTTTTATTTTAAT[A/G]CTGTGATTGTTTCAT | 8945 |
rs556447039 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514614 | TGTGCCATGATGTCC[A/G]GCTAATTTTTGTATT | 8945 |
rs556459508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422177 | TCTAACTGGCGTGAG[A/G]TGGTATCTCATTGTG | 8945 |
rs556485118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405615 | TTGGTTCAGTGTTAT[A/G]TAAAAGTCTTCTCCA | 8945 |
rs556486892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414526 | TTGTTATTTTAGAGT[A/G]GGCTACTTCTACTTA | 8945 |
rs556508092 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527622 | AGCTGGGCCTGGTGG[C/T]GCATGCCTGTAATCC | 8945 |
rs556543460 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101385602 | CTATTTTCTTTGTTC[G/T]TTCTTTCTTCTTCTT | 8945 |
rs556572408 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101475018 | TTAAAACATAGTGAA[A/T]TTTATTTTAAAAATA | 8945 |
rs556617897 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556525 | TGCAGCCCGGAGGCT[C/T]AGGGTGCAGCCTCCC | 8945 |
rs556626870 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101522976 | TTTGGGAGGCCGAAG[G/T]GGATGGATCACGAGG | 8945 |
rs556626948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451579 | AGTGTGTTTTAAGAA[G/T]GTGTGCTGTGCAAAT | 8945 |
rs556627729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101510766 | CTAAAATAAATGTAT[A/G]TTATGACCCAGACTT | 8945 |
rs556635876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101504817 | GATCTTGACTTCTCT[A/G]ACAGCAAAGATTAAT | 8945 |
rs556646843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101401002 | TTCACATCATCAGAA[A/G]TTGTGTAACCCCATG | 8945 |
rs556646982 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101458992 | GGTTTTTGAGATGGT[A/G]TCTTGCTGTGATGCC | 8945 |
rs556669821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101452030 | CATTCAGATTAACGA[A/G]GCAGCAGCAATAACA | 8945 |
rs556680463 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101449687 | TACATGATACGTATT[C/T]TTGGCTTTTTATTAT | 8945 |
rs556682166 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397612 | TTTTGGTAGCAAATT[C/T]AGAAAGCAAAGTTAG | 8945 |
rs556688964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458592 | TTTCCAATTGCCTCA[A/G]CAGTGTGTGCTATAC | 8945 |
rs556697518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497962 | GAGGCAGAGCCTGCA[C/G]TGAGCCGTGATCGTT | 8945 |
rs556705516 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101381984 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTT]GAGATGGCGTCTTGC | 8945 |
rs556713102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425752 | GAGGTCAAGGGTGCA[A/G]TGAGCTGTGATCGTG | 8945 |
rs556756983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479585 | AAAAAATACAAACAG[C/G]CATCATTTTATCTAG | 8945 |
rs556766772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522388 | AAAACAAAAAAAAAA[A/C]AACTCTAGAAATAAA | 8945 |
rs556789117 | in-del | -/AAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101491071 | CTCAAAAAAAAAAAA[-/AAA]CTCTCTTTTCTGGGT | 8945 |
rs556837820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101417983 | TATGTCATTAATGGA[C/G]TCATAGATTTCAACT | 8945 |
rs556852839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358182 | TCATAGCTTGCTGCA[G/T]CCTCAAACTCCCAGG | 8945 |
rs556859044 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101416407 | TGAAAATGTTAGAGA[-/CT]CTGAAATCATTCTTC | 8945 |
rs556871547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101472399 | GGTCTTGAATTCCAG[A/C]GCTCAAGCAATCCTC | 8945 |
rs556871726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368528 | TCTGTTGCCCAGGCC[A/G]GAGTGCAGTGGCATG | 8945 |
rs556881018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467531 | GGCAGTAGGCAAGGT[A/G]TAATTGCAATATGAC | 8945 |
rs556886757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476746 | ACTGTGCTTGAACTT[C/T]ACTATTTTTGTACTT | 8945 |
rs556895384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518637 | AGGATGATTTGACCC[C/T]GGCTACTTCTCCAGC | 8945 |
rs556915821 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357395 | GCAGTGAGCTGAGAT[C/T]GTGCCATTACACTCC | 8945 |
rs556927001 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101484662 | GTTCTTCACACAGGC[A/G]CCTCTGTCAGGTCTA | 8945 |
rs556929371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101526274 | TGAAAGATTTTTGGG[A/G]AGCCAATGAGACCAC | 8945 |
rs556940445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401669 | ACATAAAATACAAAT[A/G]TTGAGTGAATTAAGA | 8945 |
rs556941768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363188 | CAGTATTATTATTAT[C/T]CCCATTTCTCATTTA | 8945 |
rs556974611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477499 | TTTTGTTTTTGGTAG[A/C]GACAGGGCCTCGCTG | 8945 |
rs556974618 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101468873 | CCTGACAACTAAACC[G/T]TCTATTGATTAGCCA | 8945 |
rs556974975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362247 | CAGCTGTGAGCCACC[C/G]TGCCCGGCCTTGAGT | 8945 |
rs556979259 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | BTRC | GRCh38.p7 | 10:101354084 | AAGAGAGGGCGGGGG[G/T]AAGGAAGAGGAGGCG | 8945 |
rs557001137 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101395722 | GCATACTACAAAATT[C/T]ATTAAATTATCTCAG | 8945 |
rs557011228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469554 | TTCAGAAAAATAGCA[G/T]GATACATTTATTGAT | 8945 |
rs557022225 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407144 | GGGAGGATCAGTTGA[A/G]GCCAGGAGTATGAGA | 8945 |
rs557036037 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101482294 | CAAAGTGCTGGGATT[-/A]ACAGGTGTGAGCCAC | 8945 |
rs557058980 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101510276 | CACTTTAGGAGGCAG[A/T]GGTGGGTGGATCACG | 8945 |
rs557081368 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543545 | TTTTTGTATGTTTGG[A/G]TTTAAATCTATCATG | 8945 |
rs557093712 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101540439 | ACCATATATGTGTGA[A/G]TCTTCTTTGGGAATC | 8945 |
rs557093924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101501465 | AATCTCTTTAGCATC[A/G]TGTTGCCTCACTTTT | 8945 |
rs557094426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528174 | TACCTGTTAAAATAC[A/G]TTGTGTTCCCATTTG | 8945 |
rs557097384 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547376 | GAGTCTCACTCTTGT[G/T]ACCCAGGCTGGAGTA | 8945 |
rs557112933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376133 | GAGTTTGAGACCAGT[C/T]TGGCCAATGTGGTGA | 8945 |
rs557123150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368998 | GACTCCAGCTTTGGC[A/G]ACAGAGCGAGACTCC | 8945 |
rs557128549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393512 | TCATAGCAGTTAACA[A/G]GAATGCTAGGACATA | 8945 |
rs557135548 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356191 | ATTTTTAGTAGAGTC[A/G]GGGTTTCACTATGTT | 8945 |
rs557209688 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101409504 | TAGGTGAGTTCAACA[-/T]TGTGTGAACGTCATC | 8945 |
rs557218366 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510035 | GCTGCGCGTGGTGTT[A/G]CATGTCTGTAATCCC | 8945 |
rs557226855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101393972 | ACTTCGTAGACTGTA[A/G]AGCATGTCCCTCTAA | 8945 |
rs557233259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551838 | GACAAGTAACTTCCC[A/G]GACCCTGAATCTCTT | 8945 |
rs557241672 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101482262 | CTGACCTCAGGTGAT[A/C]TCTCTGCCTCAGCCT | 8945 |
rs557259355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361763 | TTGTACAGAAGACTC[A/C]GAGATAAACAAGTGA | 8945 |
rs557261561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493252 | AAAAATTTTTAAAAA[A/G]TACTAAAATCCAAAG | 8945 |
rs557270148 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366631 | TTCCAAGAATAGGAA[A/G]TAACTTGGGTAAAGG | 8945 |
rs557271384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475345 | AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGT | 8945 |
rs557280429 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101377065 | TCCCCCGCAAAAAAC[G/T]CTTATACTCTTCCTC | 8945 |
rs557281673 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383118 | TCCCAGGTTGGAGTG[C/T]TGTGGTGCTATCACA | 8945 |
rs557289519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101489767 | GACTAGTGTTTCTGC[C/T]GGTATTTGTTCCCAT | 8945 |
rs557334687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101518154 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 8945 |
rs557371398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481925 | TTGAGCCAAATAATC[A/G]GTTGGTCAATGTCAA | 8945 |
rs557396193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367752 | ACATTGTTCGTAAGA[A/T]GATTCATTCAGGTTG | 8945 |
rs557398032 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101359062 | TTTGAGGTTAACTTC[A/G]GAAGGCACTAACATG | 8945 |
rs557407790 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101537627 | TAAATATCAGAAACT[A/G]ACAACATTATTTTAG | 8945 |
rs557459494 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353325 | ATGCTTTATTTGCTG[A/G]AGGCCATTATATTCC | 8945 |
rs557470972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101520465 | AGTGTTTGGCACATT[A/G]TAGAGGTTCAGTAAA | 8945 |
rs557541653 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363551 | GCCACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 8945 |
rs557547890 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101473086 | GGACTCCAGCCACGC[A/G]TATATTCTAGATAAT | 8945 |
rs557548813 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356672 | GGTCAACTAGAAGAG[C/G]GTCACCAGAATGACA | 8945 |
rs557563704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535784 | GAAATTATGTAATTT[A/T]TGTCTTAGCATTACA | 8945 |
rs557568509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493871 | AAAACTGTGGCTTAA[A/T]TAATGCCAGGGTTCT | 8945 |
rs557584566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435174 | ATTTTATTTACCTAG[A/T]TTTTTATTTAGGTAA | 8945 |
rs557585455 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101385353 | GCCTAGGTGACAGAA[C/T]GAGACTCTGTCTCAA | 8945 |
rs557591771 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101478560 | CATTAGAAGGCTGAG[A/G]CAGGAGGATCACTTG | 8945 |
rs557603717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101386454 | AACACTGACAATGCT[A/G]TCTATCTAATTAGCT | 8945 |
rs557666182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506377 | TAAGACCTTTCCTGC[C/T]TTTCTCTGTCCTCCC | 8945 |
rs557677432 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101544655 | ACATAATCCTCTTGC[C/T]TCACAACCTCCTGAG | 8945 |
rs557688417 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556473 | CTTAGATGGCAACAC[C/T]CTCCAGTCTGTAGCA | 8945 |
rs557716161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536980 | ATGTAAAAGGGTAAC[C/T]TGTTAACAAAACAGA | 8945 |
rs557719208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439009 | CATGTGGCTACAGCA[C/T]CCCAGCTGGCAGTAA | 8945 |
rs557735614 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | BTRC | GRCh38.p7 | 10:101374793 | ATAATAAATAAAAAA[A/G]AAAAAAAGAAAAGTT | 8945 |
rs557752058 | snp | A/T | 1.74726e-05 | 0.00295567 | intron-variant | BTRC | GRCh38.p7 | 10:101532252 | AAAGAGTTTGATTCT[A/T]GGTGTTTCCTAACAC | 8945 |
rs557758176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431806 | AGCTGGATATTTTCA[G/T]TTTTCCTTTACAAAA | 8945 |
rs557774207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472575 | TCCCAGCACTTTGGG[A/C]GGCCAAGGTTGGGTG | 8945 |
rs557777764 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446929 | CACAATAGGGAGAAG[G/T]ATACAAGATTGATTT | 8945 |
rs557805638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431002 | GAGACCTTTAGGTAC[A/G]GTATTCACCTTGAGA | 8945 |
rs557848880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424109 | CGTGGTGGTGCATGC[C/T]GGCAGTCCCAGCTAC | 8945 |
rs557859833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384238 | TTTCACTTTTACAGA[A/C]GTTGGCCATCAGCCC | 8945 |
rs557869955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424935 | ACCCATAGGTAGTTT[C/T]TTCAAGCTTTACCCC | 8945 |
rs557892646 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555534 | AAAACTTGAATCGTT[C/T]ACATTTCTCAGCTCT | 8945 |
rs557903163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491076 | AAAAAAAAAAAAACT[C/G]TCTTTTCTGGGTTAC | 8945 |
rs557908821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101359573 | GCTGGAATTACAGGC[A/G]TGTACCACCTTGCCT | 8945 |
rs557914974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516525 | AAAATACTCGTTTTG[A/C]GGGGTGGTGACTAAA | 8945 |
rs557919243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432809 | CCTGTCATCCTCTCC[C/T]CATGGAGTCATGGAT | 8945 |
rs557936594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389164 | GCTGATCTTCCCATA[C/G]TAATAAATGGTGCCA | 8945 |
rs557936631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101397096 | GGCATGAGCCACTGC[A/G]CCCAGCCTGTCCAAA | 8945 |
rs557966789 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539763 | CAAACTGTTTTTCAA[A/G]GTGGTTTACCCTTTT | 8945 |
rs557983228 | in-del | -/T | 0.00239856 | 0.0345474 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557260 | GGAGTGTGTTTTGGG[-/T]TTTTTTTAACTGTTC | 8945 |
rs557996241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389863 | CTCTTGGGTTCAAGC[A/G]ATCTGTCTACCTCAG | 8945 |
rs557998715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375564 | CTGGGGCAGATATTC[C/T]GGGGAGATCAATAGG | 8945 |
rs558001400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101507233 | AGTCTTTTAAATATA[A/G]GTAACACGCAACCAG | 8945 |
rs558036502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464826 | ATTTATTGCAGTGCC[A/G]TCTGGTTTTTTGCTC | 8945 |
rs558053355 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101506878 | GAGATCTAGGAATTC[C/T]GCAGTTAATTGAATT | 8945 |
rs558065321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394508 | AGACTCAGTTGTCTA[G/T]TTTCAAAGGTAAAGC | 8945 |
rs558066133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101548792 | GGGCACAGTAGCTAA[A/G]GCCTGTAATCCCAAC | 8945 |
rs558070712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391033 | GTTTTTATAAGAATT[C/T]TGCCTAAAGAACTTT | 8945 |
rs558085183 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394678 | TAAGGGTTAAAATTC[G/T]TAGCAGTCGGGGCAG | 8945 |
rs558127489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549347 | TAAGCAGGAAAATCA[C/T]TTGAGCCCAGGAGTT | 8945 |
rs558144735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398757 | CTGTGTTGTAAACTC[A/G]TCAGTTATAAGAAAT | 8945 |
rs558148410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387554 | TTTTTTTTGAGATAG[C/G]CTCACTCTGTTGCCC | 8945 |
rs558190836 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461953 | TGAAGATAATGAGAA[C/G]TGAATTAAAGCTTAC | 8945 |
rs558215082 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540253 | TAAGTTTTATAATTT[A/T]CAGTTTGTATTTTGG | 8945 |
rs558224112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545752 | CCCCTAGTGTATGCC[A/G]TACTTTGTTATGGCA | 8945 |
rs558261045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387895 | GGGCTTTGCCATGTT[G/T]GTCAGGCTGGTCTTG | 8945 |
rs558262917 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101546663 | TTAAATTCAAAGTAA[A/C/G]TAGAAGAAAAGAAAT | 8945 |
rs558267087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101428439 | CTTGAGGTGAGGAAA[C/G]GTTGAAAACAGTGAA | 8945 |
rs558272018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433557 | AGTGAGGCTTGGTGC[A/G]TTTAAGGACCCTACT | 8945 |
rs558301983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504654 | CCTTGCGTTCCTCCT[C/T]CTGCTTTCCCATTTT | 8945 |
rs558307311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482609 | ACCGCGTTGGCCGGG[A/G]TGGTCTTGATCTCCT | 8945 |
rs558307649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362990 | TTAAGGCACTATAAG[A/G]GACTTTTGAGTATCT | 8945 |
rs558311952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519767 | TTGGGAGGCCAAGGC[A/G]GGCAGCTCACCTGAG | 8945 |
rs558314963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524895 | CAAGTCTGCTGAAAA[A/G]TGTGACTGATATCCA | 8945 |
rs558328768 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488606 | GAAGGCTTTAATTTT[A/G]GGAAAGTATATGAAG | 8945 |
rs558334083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465520 | TTTGAATAGCCTGAT[A/G]TCTATTAAATAAATT | 8945 |
rs558341809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392813 | ATAGGTGTAAGCTTC[C/T]GCACCCGACCAATTA | 8945 |
rs558360871 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | BTRC | GRCh38.p7 | 10:101434399 | TGTGCAAAACAATGA[A/C]CCTCAACGGTTATAC | 8945 |
rs558390368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457526 | GACCTCAGTTGACTG[C/T]AGTAACTGAAATTGC | 8945 |
rs558390968 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353331 | TATTTGCTGGAGGCC[A/G]TTATATTCCACCGTT | 8945 |
rs558405414 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101407876 | TACAGGTGCGTACCA[C/T]CATGCCCAGCTAATT | 8945 |
rs558420786 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553689 | TCCCTCTGTATAGCC[G/T]CTGGGACAAGAAAAA | 8945 |
rs558438437 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433603 | GTTTCAGAGAATAAA[C/G]AGAAAGGGGAGAATA | 8945 |
rs558455412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528877 | TTTTCTAATAAAGCT[C/T]TTATCTCTAAGTTTT | 8945 |
rs558461976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394097 | AAGAGATATTTCCAT[C/T]TCAATTCTATTTAGA | 8945 |
rs558468902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399540 | CAGTACCTATATTCC[A/G]TGTGCCTAGCTGTTG | 8945 |
rs558480139 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | BTRC | GRCh38.p7 | 10:101505638 | AAAATAAAAAAAAAA[A/T]AATAATAATAAAAAA | 8945 |
rs558495319 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504032 | TGCTAATGTTAGAAC[A/T]GAATTTTCTGATGCT | 8945 |
rs558515959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362946 | ATGATTTGAAATATA[C/T]GGGAGGATGTGTGTA | 8945 |
rs558519022 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101504213 | ACCAGATTCCAGACA[A/G]TTAAACTTTATTACT | 8945 |
rs558522705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101356327 | TAATCCTAATCCTGA[C/G]ATTTGTGTCAGATTT | 8945 |
rs558549656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411882 | TGAGTTTATTTTGGT[A/G]CTCTTAAGTTTTTTG | 8945 |
rs558551275 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514201 | ATACATTTATTGCAA[A/G]TGTTAATAAAAATGA | 8945 |
rs558556988 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101495096 | CTATTTTCCTCTACC[A/C]AAGAGCAGGGTTCTC | 8945 |
rs558617674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101403473 | TGAGGATTTTTGCCT[A/G]TATGGCCATAAGGGA | 8945 |
rs558618816 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101436396 | ACGCTTATAATCTCA[G/T]CACTTTGGAAGGCCA | 8945 |
rs558635314 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101440737 | AAAAAGAAAAAAAAA[-/G]GGCAACTATTTAGCT | 8945 |
rs558644136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413677 | CTTTACATTAAAGGA[A/T]AAAAAAACTTTATAT | 8945 |
rs558648175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471384 | ACAGAAAGAGAAACT[A/G]TCTCCAAAAATAGAC | 8945 |
rs558668672 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370173 | CCCAGGCTGCAGTGC[A/G]GTGGCACAATCACAG | 8945 |
rs558684365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411181 | GTTTTTTCAGTAGAG[A/G]TGGGATTTCACCATG | 8945 |
rs558686462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468717 | TTATGCTATAGGGCT[A/G]CTGAACAGATTTCTA | 8945 |
rs558692388 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401810 | GCCACTGCACTCCAG[C/G]CTGGGTGACAGAGCG | 8945 |
rs558707746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485711 | TATCTGACTGAGGCA[C/T]TTCAAGATGCTAGAA | 8945 |
rs558750459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429164 | TATCCCTGTTTTTAT[A/G]TGTGCCATGATTAGG | 8945 |
rs558755294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355475 | TTAATCTGATGCTTT[C/T]TGTATTTCCTAGGTG | 8945 |
rs558760106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101405161 | TCTGGTTCCCTGGGG[C/T]CGCCTTTTTCAGTCC | 8945 |
rs558766353 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423592 | GTGGATTTGTGGAGA[C/T]AAACACATTTGAGTA | 8945 |
rs558771378 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425474 | TGCTGTGCAGGGCTG[A/G]ATTTGTGTAGGATGC | 8945 |
rs558793592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402526 | TTTCTTGTTTAAAGG[A/G]ATTCTCATCCCTTTA | 8945 |
rs558797730 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438399 | CACTACACTCCAGCC[A/T]GGGCGACAGAGCGAG | 8945 |
rs558836935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101458188 | TACTTGGCAATAAAA[A/G]GAAAAGAAATACTAG | 8945 |
rs558874208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404390 | GTCTGTGCCATCTTG[A/G]TATTGGCATCTGTTG | 8945 |
rs558880011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101462153 | TCTTTAAGCACTGGA[A/G]CTTATATTAAGAGTA | 8945 |
rs558883564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461191 | ACAAGTGTGAGCCAC[C/T]GCACCTAGCACAACT | 8945 |
rs558884944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372127 | ATTCTTGTGCCAATA[C/T]CACACTGTCTTAATT | 8945 |
rs558887368 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492086 | GAAACACTTGCTCAA[C/T]ATGGAGCACTAAGAC | 8945 |
rs558889344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457972 | AATACATATACACAC[A/G]CACATACATCCATTT | 8945 |
rs558937030 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463672 | TTTAGATATGATGTG[A/T]CTTCCAATTTATAGA | 8945 |
rs558969128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458325 | GGCACAAATTATTGA[A/G]CCAACAAATCAGTGA | 8945 |
rs558969873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357102 | CCACTGCACTCCAGC[C/G]TGGGCGACAGAGCAA | 8945 |
rs558969981 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101365403 | TTTTTGAGACAGTCT[C/G]ACTCACTCTGTCACC | 8945 |
rs559003172 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520170 | GTTTGGGGGGACAGA[A/G/T]TCTCGCCCTGTTGCC | 8945 |
rs559003872 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496625 | TCTTACTATTTTTAA[G/T]TATACAGTTTATTAG | 8945 |
rs559003888 | in-del | -/AGA | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101430076 | TTTAGACTGATACAT[-/AGA]AGAATAGGGACAAAA | 8945 |
rs559022607 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | BTRC | GRCh38.p7 | 10:101505790 | GCTATTTTTAGAAAA[A/T]GAATTAAACATTCTT | 8945 |
rs559032207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358068 | CACAAGCACGTTTAA[A/G]ATAGGGGTTGAAAAG | 8945 |
rs559045598 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101373335 | GCCATTTAAAGTATG[G/T]AATAGTCTACGCAAG | 8945 |
rs559055190 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427267 | GGACTATAGGCGTGC[A/G]CCACCATACCCAGCT | 8945 |
rs559067409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514796 | TTGAAAGTCAGTTGG[C/T]TGTATGTATTTCTGG | 8945 |
rs559087241 | in-del | -/GACTCTT | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557150 | CCTCTTTGTTCTCTA[-/GACTCTT]AAGTACTGACTGCTT | 8945 |
rs559089563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449085 | GACATACACCTAAAC[A/G]CAGATCTTAATCTAG | 8945 |
rs559096280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371610 | TTCTTCCTTTTTTAA[A/G]GCTGAATAACATTTA | 8945 |
rs559097368 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553792 | CCATCTACTCCCCTA[C/T]GCCCCTTCAACCTTT | 8945 |
rs559107373 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101390430 | GCAAGCTTCGCCTCC[C/T]GGGTTCACGCCATTC | 8945 |
rs559132344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396499 | AAATGGAGTTCAGCT[A/G]GTATTAAGCCCACTA | 8945 |
rs559144338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424246 | TCTCAAAGAAAAAAA[A/G]AGAATCCTTGTTTTA | 8945 |
rs559152673 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101486357 | GGGCTTGTAATTGGC[A/G]CCATCAGCACGTTTT | 8945 |
rs559159114 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101498691 | ATGGTTTCTTGGTGC[C/T]AGAAAATAATAATAG | 8945 |
rs559165055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530372 | GCACTGATTAGCAGC[A/T]GCCTGGGTGACTGAG | 8945 |
rs559182542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470518 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 8945 |
rs559201550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464996 | GAACTTGATTACCCC[A/G]TTGCTGATTTTTTTT | 8945 |
rs559201599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457000 | ATGCCTAAACCACAG[A/G]TAGTTCTGAACTCCA | 8945 |
rs559205050 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101412939 | ACAGATATGAAACAA[A/G]GTAACAAAAAATGAT | 8945 |
rs559223147 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101522839 | AGATGTGTCTTTTAT[A/C]ATAACACGTCTTAGT | 8945 |
rs559238537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101472698 | CGCACACCTGTAGTC[C/T]CAGCTACTTGGGAGG | 8945 |
rs559266844 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419748 | ATGTTAGAGTTTGCC[-/T]GCTACCGTTATCCAT | 8945 |
rs559273998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479530 | TAGGCATCTTTACTC[A/T]GTATTGCTTAAGGAT | 8945 |
rs559311024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415115 | GTAACTCACCCAGAG[C/G]AACTTGCAATCCTGC | 8945 |
rs559311976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101369254 | ATGGGTTCTTGCCCT[C/T]TTGTCCAGGCTCTCG | 8945 |
rs559312017 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101361327 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 8945 |
rs559324137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362046 | GCTCACTGCAACCCC[C/T]GACTCCCTGGTTCAA | 8945 |
rs559328545 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396380 | AAGATTCTGCCACTA[C/T]GCGAAAACTTGAATG | 8945 |
rs559338839 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101521384 | GCTTTCAGCTTTTGG[G/T]TTTTATTTGTGTATC | 8945 |
rs559342281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526506 | TCCTGTGGCTGGGCA[C/T]AGTGCGTTCACGCCT | 8945 |
rs559355063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101399101 | GGGACTACAGGCATG[C/T]GCCACCATCCCCGGC | 8945 |
rs559357303 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101447628 | TTTTCCATTCCATAA[C/T]GCAACAAGTGCTATT | 8945 |
rs559377925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406905 | TTTATTGGTATACAT[C/T]AATAGATAATTGTGT | 8945 |
rs559378576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101518373 | CATCCTCCATACCTG[C/T]CTCTTTCTCAGATTA | 8945 |
rs559378779 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101517445 | ATAAAAGTAAATAAA[A/T]AAAAGAAAATAAGGC | 8945 |
rs559406151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499347 | GCTCAAGCAATTCTC[A/G]TGAGTAGCCGGGATT | 8945 |
rs559456822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482145 | CTGCCTCAGCCTCCC[A/G]AGTGGCTGGGATTAC | 8945 |
rs559465743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518863 | CTTAAATAATCCTAT[C/T]AGTTTTTTGTTAATT | 8945 |
rs559470885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101399889 | TTTCTTGTCATATCT[C/T]ACTTGCTTCAGAAAT | 8945 |
rs559481571 | in-del | -/T/TT | 0.411914 | 0.190483 | intron-variant | BTRC | GRCh38.p7 | 10:101552357 | AGCTAATTGTTTGTA[-/T/TT]TTTTTTTTTTTTTTT | 8945 |
rs559485045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549638 | AGAACGGCGTGAACC[C/T]GGGAGGCAGAGCTTG | 8945 |
rs559516765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491425 | TCCCTTGGCCTGGTT[C/T]GGCTCACACTTGTAA | 8945 |
rs559534037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101391908 | TATTATTTTTACCTT[A/G]TAAAGTGACTAATGA | 8945 |
rs559555499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482953 | ATATTGTGATATCAA[C/T]CATTTTTGTCCTTTA | 8945 |
rs559557717 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486621 | TTTCTTTATTTAAAA[A/G]GCATCGGTTTCTATT | 8945 |
rs559587355 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515254 | AGCCACCACACCTAA[C/T]CGTTTTTTTTATTTT | 8945 |
rs559590239 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367906 | GCTATTATAAATAAT[A/C/T]TTGTACAGTTTTTCC | 8945 |
rs559593725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410311 | CATTTTCCCAATGAC[C/T]GCTGATGTCAAGAAG | 8945 |
rs559600923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407562 | CACCCAGCTAATTTC[C/T]GTATTTTTAGTAGAG | 8945 |
rs559606478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101523563 | TTGTTTTCCAATTAT[A/G]GAAGTTATAGGAAAC | 8945 |
rs559639291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509874 | ACTGGCTTTTTTTTT[A/T]AAGATGCTTTTGGCC | 8945 |
rs559640667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101483414 | CCCAACCAACATGGT[A/G]AAACCCTGTCTATAC | 8945 |
rs559644045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101516160 | GAAGGCTCAGCTCCA[A/G]CAGTGTTATAAGCTC | 8945 |
rs559644131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524348 | GACATGTTACTATCT[C/G]AAGCTTATACCACTA | 8945 |
rs559644581 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489443 | TGGCTTTTTATGGGT[A/G]TAAATATTCTCCTCT | 8945 |
rs559652923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525654 | GGGGGGGTCTGAATC[A/T]TAGAGTTTGAGATGC | 8945 |
rs559653498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474837 | CCTTCCCCATTTTCC[A/G]TCTTTTTTAAGTCGA | 8945 |
rs559703450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542401 | TCTAATCACTACTTT[A/C]GCCACATCCCAAAAA | 8945 |
rs559716121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372265 | TTCTTTTTCTTTTTC[C/T]TTTTTTTTTTAAATG | 8945 |
rs559727544 | in-del | -/AT | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101440280 | ACATCTTAAAACAAC[-/AT]ATATATTTTTTCTTC | 8945 |
rs559728553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101516783 | TTATAGCAATATCTC[A/G]TTTATTTAATGTATA | 8945 |
rs559738354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101467313 | TTAATGAAGTCCCTG[A/G]TATCAGGCAGGCAGG | 8945 |
rs559739815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530784 | ACATGGGACTCCTGA[A/T]ATCAGGCTTACCTTT | 8945 |
rs559771324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354289 | GGCGGCGTCGCTGGC[C/G]TGGGCCGCCCGCCCA | 8945 |
rs559786980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101409599 | GTTGCTCCCAGGCTA[C/T]CTGGACAGCATGTTA | 8945 |
rs559789850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534565 | TCCCAGTCTGGCCCT[C/T]TCTCTAAATATAAGG | 8945 |
rs559798260 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101550957 | AGCTGTAAGGTGTTG[C/T]TAGTTCATGGAACTT | 8945 |
rs559808245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417003 | AGTTGTAAGTAAAAT[G/T]CAAATTGTTTTTTTT | 8945 |
rs559812008 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101474389 | TAATGGAAAGCCTAA[A/G]ATGTTATTACATCCC | 8945 |
rs559819531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404685 | TCTGGATGATAGTCC[A/G]TCTTGTAGTTCAGTT | 8945 |
rs559859767 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101518057 | AGCTGGGACTACAGG[C/T]GCCCGCCACTACGCC | 8945 |
rs559863831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522592 | TGCCTGGCTAATTTT[G/T]GTATTTTTAGTAGAG | 8945 |
rs559869536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441406 | TGTATTCATAGAACC[A/G]TAGAATTTCAGCATT | 8945 |
rs559905078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365082 | TTTTTTTATTTTTAT[A/T]TTTTTTTTAAGATGG | 8945 |
rs559910758 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101495293 | CTGAATTATCTAATA[C/T]TATAGCAGTTATAAC | 8945 |
rs559928547 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517584 | GCCACATTTGGGTTG[C/T]CTTAAGTAAATATGC | 8945 |
rs559940054 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101426673 | GATTTTTATGTAAAA[C/T]GGAGGAGACAAATCA | 8945 |
rs559942532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550525 | CTGACCTCGTGATCC[A/G]CATGCCTCAGGCTCC | 8945 |
rs559990932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542861 | TGGCACCTGGCCTGC[G/T]TCATGGTTTTTTTTG | 8945 |
rs559999554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433022 | CCCAACATGAATCAC[A/G]TTTGTCCAGTCGCTA | 8945 |
rs560027218 | snp | C/T | 3.34773e-05 | 0.00409115 | intron-variant | BTRC | GRCh38.p7 | 10:101535339 | TCAACTGCTCAATGC[C/T]ATTTTCTTTTTCAGG | 8945 |
rs560038740 | in-del | -/TATTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101388359 | TATTTTATTTTATTT[-/TATTT]ATTTATTTTTGTAGA | 8945 |
rs560048384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529741 | GATAGGAAATTTTCT[C/T]AACTAATTTTCAGGG | 8945 |
rs560068930 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556700 | GCTGAAGAGAGAAAT[C/G]AAAAGAGCATGATGA | 8945 |
rs560082213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101364141 | AAGATGCTTATTATG[A/G]CAACTATTGTGCTTT | 8945 |
rs560086405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434073 | AATTAAGACTAGTGT[A/G]TTACATTTTTATGAA | 8945 |
rs560142541 | in-del | -/TTTCTTTT | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398292 | AATGTGTGTTGAAAA[-/TTTCTTTT]TTTCTTTTTTTCTTT | 8945 |
rs560198325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413969 | GCTGTTGTTTTTAAC[C/T]GTGTTAATATGTACA | 8945 |
rs560211120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101431234 | GTTACGCGCCACCAC[A/G]CCTGGCTAATTTTTG | 8945 |
rs560238705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514268 | ATTTACTGACTTTTT[C/T]TTCCTTTTATAATGT | 8945 |
rs560240225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381076 | ACTGAAGTGTCAGGG[A/G]GTGCATGACTGTATT | 8945 |
rs560249401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423671 | TGTACTCTCTTGTTA[A/C]GGCAAAAGTACTAAT | 8945 |
rs560280412 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101519140 | CTGGAGTGCAATGGC[A/G]TGATCTCTCCTCACT | 8945 |
rs560292606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523945 | CTAGGGGAAAAAATA[C/T]AGACATAGAATCACT | 8945 |
rs560304321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546019 | TAGATGCATCCACTG[C/T]TATAGTTGGAGACTT | 8945 |
rs560355712 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470619 | ACAGGCGCGAGCCAC[C/T]GCGCCTAGCCGGTTT | 8945 |
rs560363933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435773 | AAAAGAGACAGTGAA[A/G]CAATTCTTCAAAGTG | 8945 |
rs560378906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541099 | TCTCTCTCCCTCTTT[A/T]TTTTTTTTCTTAATT | 8945 |
rs560389277 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101405253 | ATGGGAGGCTAGAGG[-/A]AAAAAAAAAAAGCAA | 8945 |
rs560392732 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371734 | TGTTACAAGTACCTC[C/T]TCAAGTCCGTGAGAA | 8945 |
rs560406614 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555973 | GTATTTCACTGCTGA[A/G]AACATCCTTTAACTT | 8945 |
rs560415981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101478070 | TTTGGGAGGCCGAGG[C/T]GGGTGGGTCACCTGA | 8945 |
rs560430724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101420375 | CACCCTTTTGGGATC[C/T]GACAGCTTGCACTTG | 8945 |
rs560432373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379679 | TTTAAAGTGGCACTC[A/G]TTTTTTTATGGCCTG | 8945 |
rs560465198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428750 | CGTAGTCCTATGGGT[A/G]GTAAATAAAATGAGG | 8945 |
rs560488876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498067 | ATTGACATATACAGA[A/G]AGAGTGATTTTGTGT | 8945 |
rs560489340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487874 | TCTGTGTTTTATGTT[A/C]CTTTTTTTCTTGCTG | 8945 |
rs560493719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373640 | AAGATGGGCAGGGCC[A/G]GGCGCGGTGGTTCAC | 8945 |
rs560511795 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101447931 | TATTTCCAAAAAAAA[A/C]CAATTTCTGCTAAAT | 8945 |
rs560517380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442379 | TGACTGATGGTGTGT[A/G]CTGTGCTGCTATCTA | 8945 |
rs560545307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540270 | AGTTTGTATTTTGGT[C/T]TATGATCCATTTTGA | 8945 |
rs560547688 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101439368 | TCGTGTTTCTGGTAC[A/G]TTGATCCGATGGTGT | 8945 |
rs560564380 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101480135 | CTATTAAGTATGGGC[A/T]TTGTTTCTTTTACTT | 8945 |
rs560568743 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453892 | TTGTGGGAGATAGGA[G/T]CTTTCTTGTGGCCAC | 8945 |
rs560592960 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101506131 | GTTGGTCAGGCTGAT[C/G]TCGAACTCCCAACCT | 8945 |
rs560598778 | in-del | -/T | 0.00438857 | 0.0466372 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557260 | GAGTGTGTTTTGGGT[-/T]TTTTTTTAACTGTTC | 8945 |
rs560604485 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101501195 | GCGTCTCAAAAAAAA[-/C]AAAAAGAGGTGTATG | 8945 |
rs560607288 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101443133 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 8945 |
rs560609174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447046 | ATGCAGCTAGTGTTC[A/G]CGTGCAGGTTGGACT | 8945 |
rs560634850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422786 | ATAGTTGTAGATGTG[C/T]GTTATTATTTCTGAG | 8945 |
rs560644545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101434656 | AGCAGGAACCAGGTA[C/T]AGCAGTGCATGCCTG | 8945 |
rs560674810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551528 | AGGTGGTCCATACAT[A/T]TTGTGGTATATTCAG | 8945 |
rs560696072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101454635 | AAAAACAGAAAAATT[A/G]GCCTGGTGTAGTGGC | 8945 |
rs560698220 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | BTRC | GRCh38.p7 | 10:101383985 | TCCCAAATAGTTGCC[-/G]GGTACCACAGGCTTG | 8945 |
rs560716157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400144 | CACTTGGTCTTTGAA[A/T]TTGTTATTTATTTCA | 8945 |
rs560722946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358358 | GGTCCTCCTGCCTTG[A/G]CCTCCCATTGTTGGG | 8945 |
rs560742336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385501 | TTTGTCTTATCTAAA[A/G]TGTCACTAAATTTGC | 8945 |
rs560749592 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525067 | TCTGATATGTACTTT[A/G]TAAACAGAAATAACT | 8945 |
rs560776403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101497282 | TCAAGATTATCTTGG[C/T]TATTCTTGGTTATTT | 8945 |
rs560785759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446533 | GAGAGATGAAAATTT[C/G]AGGCATTACAAATTC | 8945 |
rs560787844 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101437472 | AGTATTTTATTACAT[C/T]TAATTAAATTATGAG | 8945 |
rs560790317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483571 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 8945 |
rs560831333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401067 | AAATAATATTTAATA[C/T]AATAAATTCTATGGC | 8945 |
rs560848420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492362 | TAGCGTGACTCTGTA[A/G]TGGAATATCATGGCA | 8945 |
rs560876795 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101458518 | TAATGGTGGGGAAAC[A/C]ATCAGGAAATTAATA | 8945 |
rs560887831 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | BTRC | GRCh38.p7 | 10:101419041 | TTTGATACAGAGTCT[C/T]GCTCTGTCACCCAGG | 8945 |
rs560891209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376634 | CAGATTGTGTATCAT[C/G]TTCATTTATTTTAAA | 8945 |
rs560893128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385704 | TTCACTGAAAATCTG[G/T]TATCACAGGATCCTT | 8945 |
rs560900135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384651 | GGACTAACAGTCCAG[A/C]CAATTAGCAGTAGGA | 8945 |
rs560904985 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460845 | CTACAAATAAACTAA[A/C]CCTCCTGTTAGAACG | 8945 |
rs560909487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508866 | TTGCAGTGAGCCAAG[A/T]TTGTGCCACTGCACT | 8945 |
rs560921978 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425905 | AACAAAAACAGTCCA[A/G]ACTTTAAGTAGAAAA | 8945 |
rs560968822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449807 | GAACAGTGTAAACGT[A/G]TGTGTGGATTGCTTT | 8945 |
rs561002978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392173 | TTGATAGCGACTGGG[G/T]TTCACCATGTTGGTC | 8945 |
rs561026262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467277 | CCCTTCTTTCTGATT[C/T]GATTGATGAGGGAAA | 8945 |
rs561036899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101544034 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGACTA | 8945 |
rs561041770 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353736 | CAAGTGAGGCATTGG[C/T]CGCCATCTTGATATC | 8945 |
rs561043249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484359 | CAACGTGCTGTTTTA[C/T]GAGCACAGAGTCCCT | 8945 |
rs561178070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101468141 | TGAGGAAGGAAGACC[A/G]TATGGGGGGTTGGTG | 8945 |
rs561180894 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101365135 | CTGGAATACAATGGC[A/G]CGATCTCGGCTCACC | 8945 |
rs561186554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459082 | TGGGATTACACGCAT[A/G]TGCCAAAGTACTAGG | 8945 |
rs561190729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509680 | ACCTCAGCCTCCCAA[C/G]TAACTGAGACTACAG | 8945 |
rs561267423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101366630 | ATTCCAAGAATAGGA[A/G]GTAACTTGGGTAAAG | 8945 |
rs561267460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394879 | ATGTCTGCTTATAGC[A/G]GACAGCCCTTGAGAT | 8945 |
rs561268433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469055 | ACTAGTTTATGCTTA[C/T]GTGCTTTATATGCGA | 8945 |
rs561299750 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490950 | GTTGTCCCAGCTACT[C/T]AGGAAGCTGAGGTGG | 8945 |
rs561305339 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385564 | CATCTAATTCAAGGC[-/T]TTTTTTTTTTAATTT | 8945 |
rs561309089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464175 | ATTTAAGCTAACAAA[C/T]GAATTTTCTCTCTGC | 8945 |
rs561327558 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377527 | TAGTTGATCTACATC[C/T]GTGTCAGCATTTGGG | 8945 |
rs561347737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537068 | TTGGGTTTTTTATCT[A/C]TTTGAGTAATTTTTA | 8945 |
rs561356051 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101476961 | TCAGAAGCTCTGGGG[A/G]TGGAAACCTAGCAAT | 8945 |
rs561360415 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101552884 | AAAGCTATGCCAACC[G/T]TGGGCACTCTCAGCC | 8945 |
rs561379377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452509 | TCTTTGCAAATATAC[A/T]CAATCCCTCTGCATT | 8945 |
rs561384417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101519228 | GGATTACAGGCACCC[A/G]CCACCACACCTGGCT | 8945 |
rs561390966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101494061 | AGTGAAAATACTGTC[C/T]TAGGAAAAACACAGC | 8945 |
rs561416292 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364070 | AACTTGCACAATACT[A/G]TAGTGACAGTAATCT | 8945 |
rs561420371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444808 | GTTGAATGCACATGC[A/G]GTGCCAGCATAGCAG | 8945 |
rs561442558 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101471418 | CAGATAGATAACTAC[-/T]TTTTTTTTCATCTGA | 8945 |
rs561458244 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525622 | CAGAATGAGAAATGG[A/T]CCTAATATAGAGATT | 8945 |
rs561488537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507421 | GTTCACAAGTTAACA[C/T]GATAAAGGCTCTGTG | 8945 |
rs561490157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498245 | TGCAACCTCTGCTTC[C/T]TGGATTCAAGCAATT | 8945 |
rs561527708 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101475949 | TATATATATATATAT[A/G]TATATTCAGTAATTC | 8945 |
rs561545317 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101516081 | ATTTATGTTATACTT[C/T]AATGAAAATTAAAAT | 8945 |
rs561556993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410780 | TTTACAAAACAATAT[G/T]CATCTTTAACTTAAC | 8945 |
rs561571133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401975 | TGCTCTGGAGTTCTT[A/G]CCTCAAGCCAGTGAC | 8945 |
rs561573097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101411461 | CACTTACAATTTCCT[A/G]TAGGTCACTGAAGCT | 8945 |
rs561600702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355128 | AAGGTAAATTGTGGG[A/T]CGGTAAAATGTGGAG | 8945 |
rs561607385 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472447 | AATGTTGGGATTATA[A/G]GCATGAGCCACCCCA | 8945 |
rs561610504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448265 | TCTATTGGAGAAAAA[A/C]CATCTTTTAAAAATT | 8945 |
rs561669927 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503147 | ATAGAATCAGTGTCA[A/G]ATTATGATTTTTTAA | 8945 |
rs561671535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472651 | GAAACCCTGTCTCTA[C/G]TAAAAATACAAAAAT | 8945 |
rs561671623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463557 | AATTTACTTGGATTT[A/G]TAGCATTGTTCTAGG | 8945 |
rs561673279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520029 | AGAATCTTGGGGACC[A/G]TCTTAGAATTTTGCC | 8945 |
rs561678154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390597 | TCGGTCTCCCAAAGC[A/G]CTAGGATTACAGGCG | 8945 |
rs561730075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479868 | ATCACTATTATTATT[C/T]ATTGAGTGGCTAATG | 8945 |
rs561742086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366078 | TAAGTAAGGGGTTGT[C/T]AATTTACACCATAAA | 8945 |
rs561752346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422553 | TTGCCCATGCCTATG[C/T]CCTGAATGGTATTGC | 8945 |
rs561756291 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556854 | ACCAGCACAGCTGGC[A/G]CTCTTAGCTCCTGAT | 8945 |
rs561770063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534523 | AGGACACACTGGCAG[C/T]ATCCCATCCCCTTCC | 8945 |
rs561807205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525416 | GAAATTAAACCCATT[C/G]TTGAACTTAAACATA | 8945 |
rs561823849 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512293 | CCCTTTCCCCCCATA[A/G]TTCTCAATGCCAGAG | 8945 |
rs561829079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540150 | GCATTGACTTTTTCT[A/G]TTATGGCCTATGTTA | 8945 |
rs561851940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408644 | CCTGCTTTCTTTTGG[A/T]TTTATTTTTTGTTAC | 8945 |
rs561859366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373394 | ATGGAAAAGGAGGAA[A/G]GACATTCAAGGATAT | 8945 |
rs561882112 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554267 | GATTTGAAATGGCCA[A/G]AGCCAATCGCTTGGT | 8945 |
rs561907566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382022 | GCGTCTTGCTCTGTT[G/T]CCTAGGCTGGAGTGC | 8945 |
rs561932509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368109 | TGTTTGGATTATGGA[A/G]GTGCGTTCCTCATGA | 8945 |
rs561935756 | in-del | -/TCACTGT | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101443993 | GTACTTATATACCAG[-/TCACTGT]GCATATAATTACTAG | 8945 |
rs561948651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360275 | GCCCGGGCTGGTCTC[A/G]AACTCCTGACTTCAA | 8945 |
rs561952994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481103 | ATTTTTGGTTTTCGG[C/T]TTTTTAGAGTTGTTT | 8945 |
rs561958229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414159 | GCTCCTGGCAACCAC[A/C]ATCCTACTTTCTGAA | 8945 |
rs561967801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382732 | GTAGTTTTACCATCC[A/G]TTGGTGATTCTTCTG | 8945 |
rs562005628 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101522729 | CCCAGCCAAGACTCC[G/T]TTTACCTATCTTCTT | 8945 |
rs562011882 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101414934 | AAAATTTATAAAGTG[-/A]AAAAGTCACAGTAAG | 8945 |
rs562081925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533263 | GTAAGTTTACATTTT[C/T]GCACATTGAAGAAAC | 8945 |
rs562089564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517748 | AAACTTGGGTGTGAT[C/T]TTGTCTCCTTTTTTC | 8945 |
rs562099365 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101474301 | TGTATTTGTTAAGGT[C/G]AGGTGTATTTTGGTT | 8945 |
rs562106735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537326 | TGAGGTCAGTAGTTC[A/G]AGACCAGCCTGGCCA | 8945 |
rs562131814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101425051 | GTGAGAAAATGTGGC[A/G]TTTGGTTTTCTGTTT | 8945 |
rs562139115 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101549968 | GGAGTTTTTAATGCC[A/G]TGGAAATCTACCGAT | 8945 |
rs562139731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378999 | ACCTAATTATAATGA[C/T]AACTTACAAGATCTC | 8945 |
rs562145718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538177 | TTGTAGGTTAATCAC[A/G]TACATTTGAACTATA | 8945 |
rs562157334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549606 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8945 |
rs562184171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361250 | TAGCTGGGATTACAG[A/G]CACGTGTCACCACAC | 8945 |
rs562185083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466372 | TTGTGTAGCTGGAAC[C/T]CTGGGGATGCAAAGC | 8945 |
rs562199189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420294 | TCTTCCTGTATAATC[C/T]ATCTCCTGTTGCTGA | 8945 |
rs562214070 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557671 | AGGCAAGCAAGCTCA[C/T]ATCTGGGAGCAATTT | 8945 |
rs562232414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101439669 | GCATGAAAAGGGACA[A/G]TGTTAAAGAGAAGTG | 8945 |
rs562243832 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101541353 | CAAGCTCTGCCTCCT[A/G]GGTTCACGCCATTCT | 8945 |
rs562247810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482275 | ATCTCTCTGCCTCAG[C/T]CTCCCAAAGTGCTGG | 8945 |
rs562260434 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101354655 | ACTGGGGAAGGGAGC[A/G]CGGGATAGAGTGAAG | 8945 |
rs562279329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448995 | TGGGAAGGACACAGT[A/G]TAATAATAAGCCTAT | 8945 |
rs562282752 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510324 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 8945 |
rs562283367 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555900 | GTACAGACACGTGAC[A/C]TTTTGGTGCACACTG | 8945 |
rs562318399 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101503338 | ACTTGGAGCTTCATT[G/T]TCATTGAAAAGAGGA | 8945 |
rs562334445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485835 | TCTTCCTCAGTGAAA[A/G]GGGAGAGGTTAGGGG | 8945 |
rs562350906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371781 | GCATTTAGCTCTGCA[A/G]TCCATCTGGAATTAA | 8945 |
rs562362282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432489 | TTGAAGAATCCATAG[C/T]CTAGTTTGTTGGTTT | 8945 |
rs562363951 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505945 | TTTGAGACGGAGTCT[C/T]GCTGTGTCGCCCAGG | 8945 |
rs562367484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386802 | AGGTGAATTGGTGGG[A/G]GGTGTTTTTAATTAG | 8945 |
rs562382908 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398437 | CCTCCCGAGTAGCTG[A/G]GACTACAGGTGCCCG | 8945 |
rs562382934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550459 | CGGCTAACTTTTTGT[A/G]TTTTTATAGAGATGG | 8945 |
rs562401828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432953 | GCTCACATGGCTGAC[G/T]TCTAGTCTCTTATTT | 8945 |
rs562409437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101491160 | TACAGATCTTTCAAG[C/G]ATCTAAGTTGACTTC | 8945 |
rs562414425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364065 | GGAGTAACTTGCACA[A/G]TACTATAGTGACAGT | 8945 |
rs562419142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544924 | CTGGGCATGGTGGCA[A/C]GTGCCCAGTGCAACA | 8945 |
rs562430615 | snp | C/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101482389 | CTTTTTTGTTTGTTT[C/G/T]TTTCTTTTTTTTTTT | 8945 |
rs562442286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542221 | TATCATATTCCCTTA[C/T]TATCCTTTTAATGCC | 8945 |
rs562443819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101527508 | CTGTAATCCCAACAG[C/T]TTTGGAGGCCAAGGC | 8945 |
rs562444264 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353226 | TCACTTTTAACCAAA[C/T]CCTAGAGTTTTCTCC | 8945 |
rs562449946 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415055 | AAAGTCTATAGTAGT[A/G]TACAATAATGTCCTA | 8945 |
rs562479335 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405679 | AAATAGTTGTTCTAT[A/G]TGTTCTGTCCATTTC | 8945 |
rs562499467 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101371183 | TTTTTTTGTTTGTTT[G/T]GTGTTTTTTTTTTCC | 8945 |
rs562504810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394204 | TAATTAATTTTTTAT[A/G]ATAATGTATTCTTTC | 8945 |
rs562514121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446356 | GTCTCTTGCCTTTTT[C/T]TGTAGTGTTTGCTAG | 8945 |
rs562628835 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101520863 | TTGGGAGGCTGAGGC[A/C]GGAGAATCGCTTGAT | 8945 |
rs562637779 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101438286 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 8945 |
rs562638432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452410 | CTGCCAACCAGATTG[C/G]AATTCTCCTATCCAA | 8945 |
rs562638678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443495 | AATGTGTATGTGTGC[A/G]TACAAAACCACTTCA | 8945 |
rs562675532 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101444494 | ACCTGTTTTTCACAG[A/T]GTGTGGTAACTCCTT | 8945 |
rs562703661 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417010 | AGTAAAATGCAAATT[G/T]TTTTTTTTTCATAAA | 8945 |
rs562713273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413129 | TTTTGTTTGTTTGTT[C/T]TGGGTTTGTTTTTGA | 8945 |
rs562741028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101552801 | GCACCGCCATGCTCA[C/T]GGCCACTCAAAAGGC | 8945 |
rs562753646 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555740 | AGACAAAGTCTCAGC[A/G]CATTCCAAGGAGTGG | 8945 |
rs562768909 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381073 | TTGACTGAAGTGTCA[-/G]GGGGTGCATGACTGT | 8945 |
rs562793202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435549 | CTTTTATTGTTAAAT[A/G]TATTTCATTATATTA | 8945 |
rs562799096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436522 | CTCACCTGTCCCAGC[C/T]ATCTGGAAGGCCAAG | 8945 |
rs562816431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548087 | TGTAAAAGATTGGTA[A/C]TATCAATTTTTGGTG | 8945 |
rs562826880 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101404492 | TTATGCAACTCAGTT[G/T]TGTTTAAATTGTATT | 8945 |
rs562851410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506006 | TGCAACCTCCGCCTC[C/T]AGGATTCAAGCAATT | 8945 |
rs562912739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101390111 | AAAATAAAGCCCATG[A/G]TAGTAAAATTTTGTG | 8945 |
rs562922618 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101408988 | GGGGAGACGGAGGTT[G/T]CAGTGAACCAAGATT | 8945 |
rs562949516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441516 | CATCTAATCTCTCCC[C/T]GATCACTACCATTAT | 8945 |
rs562954400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521520 | CGTAATTGCTAATAG[A/T]ATAACAGAGTGGGCT | 8945 |
rs562980934 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101378463 | TTGGTGGTGTTAGTC[A/C]TGTCAGTACTTTATT | 8945 |
rs562982939 | in-del | -/TAAG | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515443 | ATCTCTCCATTTATT[-/TAAG]TCTTTTTAAAATTTC | 8945 |
rs562994979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429476 | CCAACAGCTTTCTAG[A/G]TGTCGTCTTCTTCCT | 8945 |
rs563001168 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438085 | TAACAAAAAATTCCT[A/G]ATTGGGTCTAACTTT | 8945 |
rs563024564 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101454444 | TTGAATAGATGAGAT[A/C]ATCTTGTGTTTATAA | 8945 |
rs563033566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101470629 | GCCACCGCGCCTAGC[C/T]GGTTTTTTCTTTTAG | 8945 |
rs563036077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101372586 | TAGAATCAGCTAGGC[C/T]GGTTGCGGTGGCTCA | 8945 |
rs563042357 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402784 | TCATGCCTTCTCAGT[G/T]GTCATGATAATTCAG | 8945 |
rs563055529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101356859 | AAGATAGGCCGGGTG[C/T]GGTGGCTCATGCCTG | 8945 |
rs563058174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461519 | TATGCTACTTTTATC[A/G]AAGAAAATAAAATCA | 8945 |
rs563070320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403881 | ATTATAGGTGTGAGC[C/T]ACTGCACCTGGCCCA | 8945 |
rs563082804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395946 | TATATATATATTCAT[A/T]GGTATTTTTTATATG | 8945 |
rs563092901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512953 | ACTTGAACAGTAGTG[G/T]TTGAGTCATCAGGCT | 8945 |
rs563102542 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504241 | ACTCCGCCTGAAACA[G/T]TAAGTAGTGGTTTTA | 8945 |
rs563120143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357373 | TTGAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGC | 8945 |
rs563145093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101453691 | AACTGAAAATAGTAA[A/G]TAAGCCACTTACTAG | 8945 |
rs563147632 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354484 | TTAATCGAGGAGGGG[A/G]CTCCAGGCGGCGCGC | 8945 |
rs563169614 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352133 | TTTATTTATTTATTT[A/T]TTTTGTAACTCCATC | 8945 |
rs563172178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550594 | GCCTCTTTATAACAG[C/T]AAACCATAGCCTTTC | 8945 |
rs563189593 | in-del | -/AAC | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101425352 | GTCATTCAGTTGGAT[-/AAC]AACAATTATAATACA | 8945 |
rs563197091 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101417363 | GGATTACACGCCAGT[A/G]TCTTGCAGAACATTT | 8945 |
rs563202877 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551666 | TCAGTTCTCGTGGCG[A/G]AAGTACATGTTCGCT | 8945 |
rs563230378 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101433136 | GGCCATTCCTTTCTT[C/T]GGTGAAGAGTAATTC | 8945 |
rs563236134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101392081 | GCCTCCCGGGTTCAA[A/G]TGTTTCTCTTGCCTA | 8945 |
rs563265193 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554429 | TTTTTTTGTTGTTTT[G/T]TTTTGTTTTGGCCAG | 8945 |
rs563289276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465138 | TTTCCTGTAGTCAAC[C/T]TCTGTAGACAAAAAG | 8945 |
rs563292762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101383962 | AAAAGTGATTCTTCC[A/G]TCTCAGCCTCCCAAA | 8945 |
rs563294741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392640 | AAATAGTTGGGATTA[A/C]GGGTGCCCACCACCA | 8945 |
rs563312109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407677 | TGACAGGCCTGAGCC[A/G]CTGTGCCCAGCCTAA | 8945 |
rs563321654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393535 | AGGACATACAGGGAC[A/G]CATAATTCATCAGTC | 8945 |
rs563323683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354361 | CGGAGCGGCTGGAGG[A/G]ATGGGATGGGAGCTC | 8945 |
rs563324056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101362520 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 8945 |
rs563361489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101500285 | ATACTGAATACTGTA[C/T]GCAATCATAACATGA | 8945 |
rs563376715 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101458042 | TAATGTTCCATCCCC[C/G]CTAAATGTTTCAGTG | 8945 |
rs563385792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101355014 | AAATACTGTAATAAG[C/G]ACAAGGTGATGAAAA | 8945 |
rs563389985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101475674 | GTTGACCAAAATCAG[A/T]TTCTTTAAAATATCT | 8945 |
rs563394451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551323 | GGAAACATCTCTTGG[A/T]GAAAGTTCACACTGA | 8945 |
rs563424595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474282 | CCTTGTGGAGGCTTG[G/T]TTTTGTATTTGTTAA | 8945 |
rs563427233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434248 | TTTAATACCATTTTC[A/C]GGTAGTTGCAGTTTC | 8945 |
rs563479154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511578 | TTGTTTTGTTTTGCG[A/G]CAGAGTCTCACTCTG | 8945 |
rs563479429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361129 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTAT | 8945 |
rs563491777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101516887 | TACTCCAGTAGCACC[C/T]AACTCATGTCCATTT | 8945 |
rs563516370 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101525254 | CCCAAGATCTGTTCT[C/G]CACTGTTTTCCTCTG | 8945 |
rs563519776 | in-del | -/T | 0.493658 | 0.0559517 | intron-variant | BTRC | GRCh38.p7 | 10:101473135 | TGACTAAGACCGATC[-/T]TTTTTTTTTTCTTTT | 8945 |
rs563528823 | in-del | -/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101445358 | TTCCCTATTTGAGAT[-/TC]TCTCTGTTAGAGCTT | 8945 |
rs563536767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466277 | ATTGAGTAGAGCTCT[C/G]TCAACTCTCTGAAAG | 8945 |
rs563544599 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353627 | GCAGATGCCAGATAC[A/G]TGAAATTTGGGGACG | 8945 |
rs563564659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484138 | ATGTTCTGTATTTTA[C/G]TTGTTATTGGTTGTT | 8945 |
rs563575210 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362218 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 8945 |
rs563576910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474940 | TGCCATTACTGGAAG[C/T]GGAACTCTTTGAGTC | 8945 |
rs563583987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408561 | ATCTGCCACCTGGGC[C/T]TCCCAAAGTGTTAGA | 8945 |
rs563588485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519868 | GGCATGGGGTTGTGC[A/G]CCTGTAATCCCAGCT | 8945 |
rs563607626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362127 | CACCACACCCAGCTC[A/G]TTTTTGTGTTTTTAG | 8945 |
rs563608740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460753 | GGTTTAGAACACAGT[A/G]ATGATTGTATATTAA | 8945 |
rs563613816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508739 | CTAACACGGTGATAC[A/C]CCGTCTCTACTAAAA | 8945 |
rs563642079 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514673 | GGCCAGGCTGGTCTC[A/G]ATTTCCTGACCTCAG | 8945 |
rs563642349 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435159 | TCTGGTTTAGGTTTT[A/G]TTTTATTTACCTAGA | 8945 |
rs563683745 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101358532 | CTGATAGATAAATGA[A/C]ACAGTATAAAGGGTA | 8945 |
rs563703587 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101552027 | CCTACCCCCTCCTTT[A/G]CCCAAAATTTTCTCT | 8945 |
rs563704876 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101408074 | GAATTAGATATTTCA[-/CT]TTTTTGTATTAAGTT | 8945 |
rs563714217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519012 | CAAGGCTTAAATCAA[C/T]CAAGGTGTTGGGCTG | 8945 |
rs563731919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357679 | CAGAATGAAATGGAT[A/G]CTCTCACAAATTTGC | 8945 |
rs563742519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358496 | GAAATAATTTTAGAA[G/T]GTATTGTTTTATTTA | 8945 |
rs563750051 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101451781 | TTGAAAATTTGCTTA[A/C]AGCCTGGGCCAATTA | 8945 |
rs563763749 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486416 | GTGCAGGAATTTTAA[A/G]GAGAAAAGCGTGGCA | 8945 |
rs563785860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401943 | GTTGATGTTAGAAAA[A/G]TTTGGTTATTGTCTT | 8945 |
rs563836850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542972 | ACCTCTGCCTCCTGG[A/G]TTCAAGCCATTCTCC | 8945 |
rs563855061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393697 | ATGATTATTGTAGTA[C/T]GAGAGTAGTGGAAAA | 8945 |
rs563874248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535555 | TCATACAAGTCTTCA[A/G]TTTTGTTATGTTTAT | 8945 |
rs563876013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101543932 | TTTGTTTGTTTGAGA[C/T]GGAGTCTTGCTCTGT | 8945 |
rs563878854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506160 | CTCAGGTGATCCGCC[A/G]CCTCAGCCTCCCAAA | 8945 |
rs563886700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396848 | CACTCTGTCACCCAG[A/G]CTAGAGTGCAGTGGC | 8945 |
rs563899945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101397901 | TTAGCTCTATCTTTC[A/T]AACTTTCTCTGTAAT | 8945 |
rs563904109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376423 | GTAAGTTGGTTTCAG[A/G]AAACAATTTACTTCT | 8945 |
rs563938532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486795 | CATGAAATATATATT[C/T]TTTATGACCAGGACA | 8945 |
rs563941329 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101541904 | TTGTTGCTTTATTTT[A/C]TGTGTCTCTGGTTGA | 8945 |
rs563942290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522666 | CCTCAAATGATTCAC[C/G]CGCCTTGGCCTCCCA | 8945 |
rs563964463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463491 | GGCCCTGTATTCATT[G/T]TTAATATAAAATTGG | 8945 |
rs563965708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479217 | TCTTTGCCCTCCTCC[A/T]TTTCTAACTTACCTC | 8945 |
rs563967530 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473424 | GAGTAGCTGGGACTA[C/T]AGGTGTGCACCACTA | 8945 |
rs563975682 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487491 | CCACTCAGTGTCTGG[A/C/G]TTTAACTAATGGCTG | 8945 |
rs563980524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409768 | GACTAAAAATGTCAT[C/T]GTGCAGTGCGTGAGT | 8945 |
rs564000211 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444520 | TCCTTGCCATAGTGC[C/T]GTAGTGTTAAAATTC | 8945 |
rs564013589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405928 | CTGCAGTTGTTGGGT[G/T]AAGTGTTCTAGATAA | 8945 |
rs564016849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526448 | TGGAAAGCTGATCAG[A/C]CCTCCTGTTTAAAAC | 8945 |
rs564048359 | in-del | -/A | 0.420892 | 0.182472 | intron-variant | BTRC | GRCh38.p7 | 10:101462680 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8945 |
rs564098498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549587 | GGTGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 8945 |
rs564104647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541250 | ATAGATGTATGTCAG[C/T]TATAGGGTTTTTCTC | 8945 |
rs564136506 | in-del | -/T | 0.3744 | 0.216852 | intron-variant | BTRC | GRCh38.p7 | 10:101427462 | CTTTTATGTTAAGGA[-/T]TTTTTTTTTTTTTTT | 8945 |
rs564141108 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429359 | CTTAGAGCTACTAGA[A/C]ATGTGTAATTTCTAC | 8945 |
rs564142775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372317 | GCTGCAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 8945 |
rs564146191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455553 | AAGGGGATAAAGGCT[C/T]CTCAGAGAAGGTATC | 8945 |
rs564162882 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101523197 | CGACAGGGCGAGACT[C/G]CATCTCAGAAAATAA | 8945 |
rs564184803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464107 | AACACTCTGCCCACT[A/C]TACAGAAACAACTGT | 8945 |
rs564194089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101424410 | ATGTATTACATGATT[A/G]TGGTATACTGCATTT | 8945 |
rs564199164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101503617 | ACCAAGACTTCCAGA[A/G]ATTACAAGTCATTTA | 8945 |
rs564211642 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530891 | ATAAATATATAATGT[C/T]GGCCGGGTGTGATGG | 8945 |
rs564256646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406652 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 8945 |
rs564325319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421679 | CTTCTGTGTCCAAGT[A/G]TTTTCATTGTTCAAT | 8945 |
rs564366299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101540030 | ATAAGTTACAAATGC[A/G]TTATCAGATGTAATT | 8945 |
rs564398792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101389676 | CCAGGCTGGAGTGCC[A/T]TGGAATAAACACAGC | 8945 |
rs564399896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530842 | ATATGGAATGGTAAC[C/T]GTGAAAACACTTTCA | 8945 |
rs564411747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422426 | TTCTGTAGGTTGCCT[A/G]TTCACTCTGATGGTA | 8945 |
rs564415359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533146 | ATAGATAGTAATTTT[A/G]TATATATCGGCACAG | 8945 |
rs564416339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413290 | CTGGGATTATAGGTG[C/T]CCACCACCACGCCTG | 8945 |
rs564418509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101470921 | CAAACCATTTAGTTA[C/T]ATAAGAGTTATATTC | 8945 |
rs564436325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373281 | ACTTAGTGCTTTAGA[A/G]TGGATTAGACTAGGG | 8945 |
rs564443803 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544174 | TCAGGTTCCCAAAGT[C/G]CTGGGATTACAGGCA | 8945 |
rs564453482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524474 | CAATCTAATGCTTTA[G/T]GGCCATTTAAACTTA | 8945 |
rs564474957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381814 | ACATGATATTTTACC[G/T]TCTGCATGTATTTTC | 8945 |
rs564497406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552654 | CTGCCATCCACACAG[A/C]TGTCCTTGAAGATAG | 8945 |
rs564504294 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101490413 | TCTCATGTGAACCTG[G/T]TGAGATGGACTGGAT | 8945 |
rs564507373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544077 | ACCACACCCAGCTAA[A/T]TTTTTGTAGTTTTAA | 8945 |
rs564509808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482213 | TTAAGTAGAGACAGG[A/G]TTTCGCCATGTTGGC | 8945 |
rs564522167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375076 | GACGCAGGGGAACTT[A/G]GCAAGGGAAGGTGAT | 8945 |
rs564545129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544830 | TTGGGAGTCTGAGGC[A/G]GTGGATTGCTTGAAC | 8945 |
rs564551363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427122 | TTCTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 8945 |
rs564554042 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415112 | TCAGTAACTCACCCA[C/G]AGCAACTTGCAATCC | 8945 |
rs564559069 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435371 | CTGTACCCATCCCCC[A/G]TATGCAATTACTGTT | 8945 |
rs564584344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473599 | CCTCTGCCTCCCAAG[C/T]AGCTGGGATTACAGG | 8945 |
rs564589445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427676 | TAGGACCACAGGCAT[A/G]TGCCACCATGCCCAG | 8945 |
rs564594608 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101492997 | GTTTAGGTTGCTGTT[A/G]ATTGCAAATTACTAG | 8945 |
rs564617037 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511091 | TCAAAACCTCCAGGG[A/G]CTCTCCTTTACACTT | 8945 |
rs564625385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101489391 | TTCCTTAATCTGAAA[A/G]AGAGATTTTTATTCT | 8945 |
rs564632090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534087 | AAATTCTCAAGCTAT[C/T]CAAGGGCCCCACACT | 8945 |
rs564638381 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101445714 | GCTTTGGTTTAATCA[A/G]TAGAATAATTGATAA | 8945 |
rs564638544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447107 | GCTTATCTTGAGGGA[C/T]GCAAGTAATAGACCA | 8945 |
rs564663147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398203 | TTATATTACAAATAA[A/G]GTGGAAGAAGGTGGA | 8945 |
rs564670876 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358269 | CTGGCTATTTTTTTT[C/T]TCTTTTTTGTTTTTG | 8945 |
rs564677801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386686 | GTGTCACAATTGATG[A/G]CAGCCTGAATTAGAG | 8945 |
rs564703142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401896 | AGAGTGCTTAGCAGG[G/T]CAAAAAAAGAAGGAA | 8945 |
rs564746045 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101377927 | CTTGTGGCCTTTAAT[A/C]AACTGAGGAGATAGG | 8945 |
rs564773190 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101480734 | ATATAACCATCGAAA[G/T]CATACATATAAGAAA | 8945 |
rs564789968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479859 | AATTATTATATCACT[A/G]TTATTATTTATTGAG | 8945 |
rs564806337 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509039 | CAGTTTATCTTGAAA[C/T]CTCCTTGTAAAAGGA | 8945 |
rs564810523 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394277 | ATAAATTTTGGAAAT[A/G]GGATATTTTTAGATC | 8945 |
rs564812907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393673 | GTCACAGAGAAGTCT[A/T]CTGTGTTGATGATTA | 8945 |
rs564833713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551982 | TCAGGAAAAACTGGT[C/T]ATGAGTATTAATATT | 8945 |
rs564861639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537930 | AAATCAAAAGATGAG[A/G]GCTTGCTTATATAAA | 8945 |
rs564871311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484522 | CAATGCAGACGTTTG[C/T]ACTTCCTCTGGGTCT | 8945 |
rs564891688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370404 | CAGGTGTGAGCCATC[A/G]GGCCCGCCCCTTCTT | 8945 |
rs564904743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453592 | TGACTTTTCATCACT[G/T]TGTAAATTAGTTTAA | 8945 |
rs564908012 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485065 | AGCAGATTGACTGCA[C/G/T]ATTTGTTGTGTAATC | 8945 |
rs564940856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101454203 | TTATCTGTATACTTA[C/T]GTAATGTGTTAGTGG | 8945 |
rs564988066 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101451097 | GGAATGTTTGTTAGA[A/C]TTAAAATATTACTTT | 8945 |
rs565007304 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BTRC | GRCh38.p7 | 10:101477033 | CCACGCTGGAGTGCC[A/G]TGGCACGATCTAGGC | 8945 |
rs565020324 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372342 | GCTCACTGCAACATC[C/T]GCCTCCTGGGTTCAA | 8945 |
rs565028287 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101446280 | TATTCTAAATGTGAG[C/G]TCTTTTGTCCCTCAC | 8945 |
rs565030369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411178 | TTTGTTTTTTCAGTA[A/G]AGATGGGATTTCACC | 8945 |
rs565039260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101460126 | ATTTCATGACCTGAA[A/G]GAGAGTTACTTGCAA | 8945 |
rs565039475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450677 | ATTTTAGCTTTGAAA[C/T]AACTGTTAGTGCTGC | 8945 |
rs565044801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390622 | CAGGCGTGAGCCACC[A/C]TGCCTGGCCTGGTAT | 8945 |
rs565153291 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101547832 | AGATTTATGCCAGGT[A/C]TGCAAGGCTGGTTCA | 8945 |
rs565160579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101501987 | CTTTTCTCAGAAAGA[C/G]CAAAAATCTGCAATC | 8945 |
rs565161097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420015 | TTGCTCCTAGGCCCT[C/T]TCAGTTGGTAGTCAG | 8945 |
rs565163006 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101459038 | CTCCTGGACTCAGGC[A/C]GTCCCTCTGCCTCCA | 8945 |
rs565175455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443319 | TTTACTGATTTTTGT[A/G]AAACATGCAAATGTA | 8945 |
rs565187541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493432 | TTTGCCCAAGGTCAT[A/G]CTGTATGTTGCAGAA | 8945 |
rs565206882 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101505205 | CACGAGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 8945 |
rs565222648 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101490087 | TATCATAATTCTAAG[-/T]TTTCTCTCCCACCCC | 8945 |
rs565230730 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554477 | AATATTGATCTCACC[A/G]TGTCAACCTTGCACT | 8945 |
rs565241007 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517810 | AGTAGGATCTGTCTT[C/T]AGAATATACACTGAA | 8945 |
rs565244105 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101395064 | GTAACAAAATTGTAT[A/C]ATCTTGTGTATAGCC | 8945 |
rs565246249 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101550934 | CTGTGGGTAGGAGAC[A/G]GGATATTAGCTGTAA | 8945 |
rs565246690 | snp | G/T | 0 | 0 | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101515817 | CTCCCAGGCTAAACT[G/T]TATCAAATTTATTTC | 8945 |
rs565251591 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461108 | AGTTTCAGCATGTTG[A/G]CCAGGCTGGTCTCAA | 8945 |
rs565256049 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530549 | AGGTAATAGTTACCA[C/T]TACTAACAAAATTTC | 8945 |
rs565261406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437830 | TGTCTTTGCATATAC[C/T]GTTCTGCTTACCTGA | 8945 |
rs565264628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101513826 | TGTTTGGTAAGTATA[C/T]GTTTAACTTTACAAA | 8945 |
rs565323102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101488575 | AAATCAGCTTCTGTT[C/T]CCTAGACCTTTTTTG | 8945 |
rs565380268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469910 | TTCCTCTATGTTGCT[A/G]TGTATATCAGTAGTT | 8945 |
rs565404582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356617 | TTTAGTTACTTTCAT[C/T]ATTGACCTTGCCTGC | 8945 |
rs565429577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469084 | GATATAAAAACGTAT[C/T]AAAGTACTCCAACGC | 8945 |
rs565431390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101477793 | TAGCTGGAACTACAG[A/G]CACCCACCACCATGC | 8945 |
rs565451959 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101411602 | ATTATCATTTCAAAC[A/T]TTGTATTTTTCATTC | 8945 |
rs565479856 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101374746 | ATGTATGTAACCTGC[A/G]CAATGTGCACATGTA | 8945 |
rs565493807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455093 | TTGAGACAGGGTCTC[A/T]CTCTGTCGCCCAGGC | 8945 |
rs565505183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438935 | TGGAAATGTGCCTAT[C/G]GACTATTTACAGTGA | 8945 |
rs565507332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381309 | TACTTTTTCCAGATC[A/G]AACAGTTTGTGAATG | 8945 |
rs565537913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520682 | CAAGTTGTTGGCCGG[C/G]CACGGTGGCTCATGC | 8945 |
rs565559362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101403015 | AATCTCTTTTTCTCT[A/G]CTAGATTATAACCTC | 8945 |
rs565577182 | in-del | -/T | 0.496314 | 0.0427728 | intron-variant | BTRC | GRCh38.p7 | 10:101415187 | TTTTATCTTTTTGTC[-/T]TTTTTTTTTGAGACA | 8945 |
rs565582166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455879 | GGGCATGGTGGCTTA[C/T]GCCTGTAATCCCAGG | 8945 |
rs565599286 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415572 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGCCCATG | 8945 |
rs565623156 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101506797 | GCTATAGTGTACTCA[C/T]TGTTTCACAAAGGGT | 8945 |
rs565624561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512880 | GAGGGAGATGTGCAG[A/G]GGTGGCAGAAATTTA | 8945 |
rs565635866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448458 | ATTTTGTTGTTTGGT[G/T]ATGTTAACAAATGAA | 8945 |
rs565656726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498374 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGAACTCA | 8945 |
rs565672946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439774 | TAGTGTATTATTAAT[A/G]GTGGAATTTATGGAA | 8945 |
rs565684598 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497793 | TTGGGAGGCCAACGC[A/C/G]GGCATGTCACAAGGT | 8945 |
rs565711998 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101549251 | CAGCCTGGGCAACAA[A/C]AAGACCTAATCTCTA | 8945 |
rs565761033 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515466 | TTTAAAATTTCCCTC[A/G]GCAATGTTTTATAGT | 8945 |
rs565762537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399473 | AACAGTTCAAAGATT[A/G]CATTAACAAGCTAGC | 8945 |
rs565786839 | snp | A/T | 0.00021881 | 0.0104574 | intron-variant | BTRC | GRCh38.p7 | 10:101521612 | CAATACTAATCATTT[A/T]ATGTTTCTTTTAACC | 8945 |
rs565807544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432535 | TTTTTTAACCTTTTC[A/G]GGGTTGCAGTTAGTT | 8945 |
rs565820362 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101542597 | TTTTGTTTGAGACAG[G/T]GTATCACTATGCCGC | 8945 |
rs565825670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391615 | CATGTACCTTAATTT[A/G]CTATGTTCTTTTAAA | 8945 |
rs565833959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484044 | TGTTTGAATACATCT[A/G]TCCAGATTCCTGGCC | 8945 |
rs565837805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392339 | CCAAAGAGAATGAAT[A/G]AGGGAAGAAACCATT | 8945 |
rs565857718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358800 | TAAATCCTAGATTTG[A/G]AAGTCCAAGAATGTC | 8945 |
rs565888655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101466496 | GGGCATTACATTTTC[C/T]TCCCCCATGCACCTC | 8945 |
rs565908288 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406207 | TTTGAGATGGAGTCT[C/T]GCTCTGTCTCCCAGG | 8945 |
rs565917958 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539577 | ATTGTATGGTTATAC[C/G]CATTCACTGATTGTT | 8945 |
rs565924115 | in-del | -/TGTTT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101543510 | TCTCTGCCTTTGTCA[-/TGTTT]AGACCATTTATGTAA | 8945 |
rs565938417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523963 | ACATAGAATCACTAT[A/G]TATTAAGGAATGTGA | 8945 |
rs565950358 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353803 | ACCACGGAGACACCC[G/T]TGCCCCTCCCGTTTC | 8945 |
rs565950737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368151 | CCATCCTTTTGGAAA[A/T]AAGTGAGTTCTCGCT | 8945 |
rs565962709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508334 | AAATCATTCAGATTC[A/G]TAATGTGAACTTTCC | 8945 |
rs565966713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408922 | GGCGTGGTGGTGGGC[A/G]CATGAAAGCCCAGCT | 8945 |
rs565970287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101397077 | CCAAAGTGCTGAGAT[A/T]ACAGGCATGAGCCAC | 8945 |
rs566034294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458212 | ATACTAGTATTTACA[A/G]CAACATGAGTAGATC | 8945 |
rs566096139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375213 | TTTTGTGCTGTTTTC[A/G]TGATAGAGTTCTCAC | 8945 |
rs566098593 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485492 | TAGTGCTGATTCTGG[A/T]TGGCCCTTGAATATA | 8945 |
rs566108380 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101532805 | GCGCGTGTGCGCGCG[C/T]GCGCGCTTAGCTATA | 8945 |
rs566151009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520960 | AGAGCAAGACTGTCT[A/C]CAAAAACAAAAAAAA | 8945 |
rs566157837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359550 | CTCCTGCCTCAGCCT[C/T]CTAAGTAGCTGGAAT | 8945 |
rs566158920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449893 | TACAGTGGTATAAGA[C/T]GCCTGCTTTGCAAGC | 8945 |
rs566159018 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556174 | CTGTGAGACCCCTAC[A/T]TCATTCTGGTTTTTT | 8945 |
rs566159132 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101403414 | TTAGTCATGGTGTAT[A/G]TTCCTTTTTCTGTGT | 8945 |
rs566162304 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449087 | CATACACCTAAACAC[A/G]GATCTTAATCTAGCC | 8945 |
rs566211638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101499836 | TTCTTTCAAATGGAA[A/G]TCAAGCCTCAGTGCT | 8945 |
rs566218644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394644 | AGAAGAAATAAAGAA[A/G]TCCCTATTTCAGAGA | 8945 |
rs566219956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537401 | GGTGTGGTTGCGGGC[A/G]CCTGTAATCCCAGCT | 8945 |
rs566231258 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421159 | ATTCATTTTTCCTTA[C/T]GATCAGTTATCCAGT | 8945 |
rs566232047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101541685 | TCTACATCCATTGAG[A/G]TAATCATATGGTTTT | 8945 |
rs566280500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370620 | TTCCCTCCCTCCCTC[C/T]CTCCCTTTCTCCCAT | 8945 |
rs566332968 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101356313 | AGAGGGTTGACTCTT[A/C]ATCCTAATCCTGACA | 8945 |
rs566337460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527913 | ACCTACTTCATACTT[C/T]GGAAATAAACTCTTT | 8945 |
rs566345242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371239 | GCCCAGACTGGAGTG[C/T]AATGAATGGCACCAT | 8945 |
rs566375732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101407763 | CAGTCTCGTTCTGTC[A/G]CCAGGCTGGAGTGCA | 8945 |
rs566379738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101465465 | CAAATTCCTTGAAAA[A/T]TACAACTTACCAAAA | 8945 |
rs566410523 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101456434 | TAAAAACTGACTCTG[A/G]GGATTTAAGTCTAGG | 8945 |
rs566428378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461081 | CTAATTTTGTATTTT[C/T]AGTAGAGACACAGTT | 8945 |
rs566447908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101410972 | GAAACAATTTTAAAA[A/G]TATTGACATTTGTAT | 8945 |
rs566503322 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101453053 | AGTTTGAGTGATTTT[A/G]TCCATGTAGCTAAAA | 8945 |
rs566503566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429677 | TTTGGGTTGTTTCTT[C/T]CCCTCGCCTTATACC | 8945 |
rs566510759 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101397221 | ATACAATCCTAAAAT[A/G]AAGTTGTTACATATT | 8945 |
rs566512635 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362686 | AGGTGTGAGCCACCA[C/T]GCCCGGCCAGAAGAA | 8945 |
rs566518828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101544984 | TATGAGTCCAGGAGA[C/T]TGAGGCTGCAGTAAG | 8945 |
rs566544156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101485262 | TAAGAGTAATTGCTT[A/G]TGCAGTCTTCTTGCT | 8945 |
rs566549793 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406832 | AGCCACCGTGCCCGG[C/T]CTCAGCTTTCTTATG | 8945 |
rs566557910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537408 | TTGCGGGCGCCTGTA[A/G]TCCCAGCTACTTAGG | 8945 |
rs566561080 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460860 | CCCTCCTGTTAGAAC[A/G]TTATGACTATATGTA | 8945 |
rs566562636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387347 | TTCAATATTCTCCTA[A/G]CTATTTGAACTATAT | 8945 |
rs566577233 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369931 | CCCCACACCCACTAT[A/G]TAGATGCCGTCCTTG | 8945 |
rs566580027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101477345 | CAGATGATTCTGATG[C/T]GCACTAAAGTTTGAT | 8945 |
rs566629748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101536707 | CGTCTTAATCCTTCC[A/T]TATGTTTATGGTGTT | 8945 |
rs566646716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101427316 | AGAGATGGGGTTTCA[C/T]CGTGTTGGCCAGGAT | 8945 |
rs566667390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411732 | TTTTTCTGGGTCTGC[C/T]TCCATTGACTGATAG | 8945 |
rs566677714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101363616 | GGTGTGCACCACCAC[A/G]CCCGGCTAAGTTTTG | 8945 |
rs566682555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101427952 | AAGCATTCTTAATAC[A/G]TATAAAGAAGTAATA | 8945 |
rs566685121 | in-del | -/T | 0.0111709 | 0.0742127 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352128 | TTTATTTATTTATTT[-/T]ATTTTTTTTGTAACT | 8945 |
rs566693525 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554310 | ATGGTTTCCATCTCC[A/G]ATTTCCTCATCAGGG | 8945 |
rs566703681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468593 | GTTTGCTTTTTCTAT[A/G]CCATATTCTTGTGTG | 8945 |
rs566711307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411146 | CATTACAGGTGCAGG[A/C]CCCTACGCCTGGCTA | 8945 |
rs566725112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437262 | GTTCTCCTAATAAAA[G/T]GAATTATTGTTTATT | 8945 |
rs566754327 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555132 | GTTGACTATTAATGG[C/T]TTTTTGATTGGGTAA | 8945 |
rs566765162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422060 | ACACTGTCTTCCACA[A/G]TGGTTGAACTAGTTT | 8945 |
rs566770843 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459964 | TATAGTATCTTTGGT[A/G]TGACAAACTTCCAGC | 8945 |
rs566772642 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101372900 | CAGTTTCCACAAAAC[A/G]TACTTTTATGATTTT | 8945 |
rs566774944 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457806 | ATTTCTTAACATTTT[A/G]TTATGGATTTAATTA | 8945 |
rs566775291 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101491456 | TCCCAGTACTTTGGG[A/C]GGCTGAGGTGGGAGG | 8945 |
rs566791325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101469287 | AGTGGTAAAGGAACT[A/G]TGACAAATTTTAGTT | 8945 |
rs566802928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413651 | AAAGATGAAGATGTC[C/T]CAGAGGAAATCTTTA | 8945 |
rs566809559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101429047 | CTTTCTACAACTATA[A/T]TGTTTTAAGGAGAAA | 8945 |
rs566824010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101372693 | AACATGGTGAAATCC[C/T]GTCTCTACTAAAAAT | 8945 |
rs566832909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420957 | ATCTCTGTAATCGCT[A/T]CAGGTTTATACTCAT | 8945 |
rs566881161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531121 | GGTTGCAGTGAGCCA[A/G]CATCACACTGCTGCA | 8945 |
rs566887283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365300 | CTGGTCTTGAACTCC[A/G]GATCTCAGGTGATCT | 8945 |
rs566896262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433256 | ATACATATATAGATG[G/T]TTATTATATTTCTAT | 8945 |
rs566909177 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BTRC | GRCh38.p7 | 10:101399989 | TTGTCTAACCTCAGT[A/G]ATAACCATACCATCA | 8945 |
rs566946456 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355284 | GGAAGTAAGTCAGGG[A/G]TAAGTCAGGATTTGT | 8945 |
rs566966708 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101522195 | ACAGGCGCCCGCCAC[C/T]ACACTGGGCTAATTT | 8945 |
rs566969428 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101414227 | ACAGTACAGGCATGC[A/C]CTGTATAATGACATT | 8945 |
rs566973113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101472235 | TTTCTCCCTTCCTTC[C/T]TTCCTTCCCCTTCCT | 8945 |
rs566978784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101431113 | ACGGAGTCTTGCTTC[A/G]TGGCGCAAGCTGGAG | 8945 |
rs566996153 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101422171 | CACCATTCTAACTGG[C/T]GTGAGATGGTATCTC | 8945 |
rs566999343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101366253 | GATAGTGTACCTGTA[A/G]TGTAATTTGATAAAA | 8945 |
rs567003749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522812 | ATCTTTTCTGAGGTG[C/T]TACCTGGTGTAAGAT | 8945 |
rs567033246 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101496226 | GAATATATACAATGA[A/G]TGTATTTGAATGGGT | 8945 |
rs567035208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101547374 | CGGAGTCTCACTCTT[A/G]TTACCCAGGCTGGAG | 8945 |
rs567056493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495616 | AAGATATAGTCTCAG[A/G]CTCTTCTGTGGCAAA | 8945 |
rs567074570 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373493 | GCTGGCATCAGTCAT[A/G]TTAAGGGCAATTAGA | 8945 |
rs567098371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546507 | TGAAGTAAATAAAAA[C/T]GAAAACACAGCTATC | 8945 |
rs567124225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424741 | AATTGTGCCATTGAA[A/C]CTGATGGGCACTAGA | 8945 |
rs567132261 | in-del | -/ACAA | 0.00517822 | 0.0506191 | intron-variant | BTRC | GRCh38.p7 | 10:101479577 | AGTTAAGAAAAAAAT[-/ACAA]ACAGGCATCATTTTA | 8945 |
rs567133115 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526254 | ACCTGGCCATTCACA[A/G]TCACTGAAAGATTTT | 8945 |
rs567135493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538797 | TCATGCCTATTATCC[C/T]AGCACTTTGGGAGGT | 8945 |
rs567140135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496515 | CGAGCTCCTGGCCTC[A/G]GGCAGTCCTCTTGCC | 8945 |
rs567141839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486309 | AGTCCGCATAAATCT[C/G]CCCGAATGGTGGGGG | 8945 |
rs567157692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101478526 | CTGAGCACAATGGCT[C/T]GTCCCTGTAATCCCA | 8945 |
rs567173166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440874 | AAAGAGAGAAGATAA[C/T]ACTTGTAAAATATAA | 8945 |
rs567190771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380329 | ATAAAGGACTGTAAG[C/T]ATCCAGATCATGTGT | 8945 |
rs567201296 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101468423 | GTGGGAGGAAGCCTG[-/T]TGTGCTCATCTGCAT | 8945 |
rs567208073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432684 | AGGACTTAGAATTCA[C/G]TGAAAACAATTATAC | 8945 |
rs567210450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101372056 | TTTTGTCATATTAAT[A/G]TCTATATATGTATGT | 8945 |
rs567222858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375990 | AGGTGAGGCCTTGTA[C/T]TTGGGAAACACAGCA | 8945 |
rs567236067 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546449 | TGGGTACATAGTAGG[A/T]TTATATATTTATGGG | 8945 |
rs567247795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483136 | TACCTTGATTGTAAC[C/T]CTTTGCCAGAAATAT | 8945 |
rs567264221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425385 | TTGTTATACTCTTCA[A/G]CTTTCTTTGATTTTG | 8945 |
rs567281031 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101518027 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 8945 |
rs567300392 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101420620 | GCTCTGTCACCTCAT[C/G]CTGGGTCCCCCTCCC | 8945 |
rs567306039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492952 | GTAAGTACTAAGTGA[A/G]ATTTTATAAAACTGA | 8945 |
rs567361256 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101416027 | AGATTTGTGTAAGTA[C/T]ACTGTGATCACACAG | 8945 |
rs567367283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535663 | TTTTGTTGCCCTTCT[C/T]TTTAAATTTCTCCTG | 8945 |
rs567378566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101550129 | CTCTCATCCACCCTA[C/T]GCCAAAAAGGGTTGG | 8945 |
rs567380309 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398232 | GAGTTCTGTAAGACC[A/G]GACACATGCTATAAA | 8945 |
rs567381033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361440 | ACAGAAGTCCTTTCT[A/G]AATGTGTATAGTGAG | 8945 |
rs567383795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408998 | AGGTTGCAGTGAACC[A/G]AGATTGTGCCACTGC | 8945 |
rs567394188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493629 | CAGGATTTGGAAATC[A/G]CAGAAGTATGCAAAT | 8945 |
rs567397560 | in-del | -/TT | 0.0074598 | 0.0606156 | intron-variant | BTRC | GRCh38.p7 | 10:101473208 | TCAGTTTATCTATCT[-/TT]TTTTTTTTTTCGGTT | 8945 |
rs567398541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376933 | AAATTTTTGATTCCA[A/G]TTTTTTTAATGGACA | 8945 |
rs567415937 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101449270 | AGGGGATGAAAGTCA[C/T]TTAGCAAAAAGAAAC | 8945 |
rs567421925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391558 | GCTCTTTGTTCATCT[A/G]ATGTATGTTGGAGAG | 8945 |
rs567429971 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101548701 | AAGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 8945 |
rs567452943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499014 | AAAAACAGAAAAAAA[A/T]AATAATAATAGCCAC | 8945 |
rs567489913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384009 | AGGCTTGTATCACCA[G/T]GCCCTGTCTAGGTTA | 8945 |
rs567500380 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369480 | TTTGGTGTCATTGAG[C/T]ATTTTCTTGTTTACT | 8945 |
rs567511308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101451920 | GCCATTCATGTGAGC[C/T]CAGTCCACCCACTCT | 8945 |
rs567514589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467435 | GTTCTGATAATTGCT[A/C]GAGAAAACCCATTCC | 8945 |
rs567542583 | snp | A/G | 0.000164726 | 0.0090739 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550801 | TTCCTAAATGATCCA[A/G]CTGCCCAAGCTGAAC | 8945 |
rs567543846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101383418 | AAAAAAAAAAGGCTA[A/G]TCAAGTTCTGAAGCA | 8945 |
rs567558873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484813 | GAAGGAACTTCAGAT[A/G]TAATATTCTTTTTGA | 8945 |
rs567561615 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487749 | AATGAGAAGAACAGT[A/G]TTCTGTGATCAACCT | 8945 |
rs567566397 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101401076 | TTAATACAATAAATT[A/C]TATGGCAATAAAAGA | 8945 |
rs567585828 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457036 | ACTATGTTTTTTCCT[A/G]TGGACACATACCTAT | 8945 |
rs567588612 | in-del | -/TTTTCT | 0.00716266 | 0.059414 | intron-variant | BTRC | GRCh38.p7 | 10:101372242 | TCTTGGCCTTTTGCG[-/TTTTCT]TTTTCTTTTTCTTTT | 8945 |
rs567600834 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101518943 | AATTCTGTGTGTAGT[A/T]CTGAGGGTCAGAAGT | 8945 |
rs567609293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442749 | TAGAAAGGATAAATG[A/T]TACAGGGCTTGTTCA | 8945 |
rs567632814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551732 | GAGGACAGTGATTCA[C/T]GCCCAGCTGGGCTGT | 8945 |
rs567701040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496838 | TAAATTCTGGATACA[A/G]GTTATTTGTCTGATG | 8945 |
rs567710393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434478 | GAGTTAACATGTATA[A/G]AACTAATAGAAAATG | 8945 |
rs567731629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544518 | AGTCTCAAGCAGTCC[C/T]CCTGACAGCTTCCCA | 8945 |
rs567735135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506232 | CTGGCTAGTTTTCCA[A/G]ATTTTTTTACCTTTC | 8945 |
rs567746747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434895 | CCACCTCGGCCTCCT[A/C]AAGTCCTGGGATTAC | 8945 |
rs567759260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354520 | CCTGGAGGGAAAGGG[A/G]CGTGGGGACTGTTAC | 8945 |
rs567766351 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101431541 | TGACTGAGTCTTATC[-/TG]CGTACCTCAGGTATT | 8945 |
rs567768934 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459640 | ACCATTTAAATATTC[-/T]TTTGCCCTAGTGGGA | 8945 |
rs567770762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497642 | GCTTGGGAGGTTGAG[A/G]CTGCAGTGAACCGTG | 8945 |
rs567793131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380587 | AAGAACCTCTTTTAA[G/T]TAGCAAACTTCCTTC | 8945 |
rs567821642 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101495548 | CTCTAACCTTGTTCA[A/G]AGTGGTGGCATATGG | 8945 |
rs567905811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510186 | TACAAAGAAATCAAA[A/G]GAAAATAATCGGAAA | 8945 |
rs567909190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101471041 | GTAGACAAGGCGGAC[A/G]AGAAAAATGATAGGT | 8945 |
rs567909430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510846 | CTCTGTCATGAGAGT[A/T]AAAATACCTTTCTTT | 8945 |
rs567911269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356986 | TACAAAAAATTAGGC[A/G]GGTGTGGCAGCGTGC | 8945 |
rs567929187 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101389019 | TGATGATTTCTAATG[C/G]GCTAATAGTCTCTAA | 8945 |
rs567954281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101393233 | TCGCCCATACCTTGT[C/T]CTATGGGTCTCTTCA | 8945 |
rs567970674 | snp | C/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101451423 | ATACATCAGCCAGAA[C/G]AAGCATAATTGGTTG | 8945 |
rs567990149 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101384529 | CTAGTTAGTAAGTTC[-/TG]TGTGTTTTTTTAAAG | 8945 |
rs568009922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455859 | GAATGATGATTCTAA[A/T]GGCCGGGCATGGTGG | 8945 |
rs568016857 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557231 | ATATGTTCACAACCT[A/C]GGATCATGATAATGG | 8945 |
rs568022385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446790 | TATGAGCAAAACTTT[A/T]AAAAAAATTAACCAT | 8945 |
rs568059333 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | BTRC | GRCh38.p7 | 10:101505644 | AAAAAAAAAAAATAA[A/T]AATAAAAAAACAAAT | 8945 |
rs568062640 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463055 | TATTTTGGGGTTTTT[-/G]TTTTTTTTGAGACAC | 8945 |
rs568077258 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101503242 | GTCTCAGTGCATATG[C/T]AAACCTCTTTTGGTT | 8945 |
rs568089072 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556183 | CCCTACATCATTCTG[G/T]TTTTTTTGCTTGAGT | 8945 |
rs568111337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438166 | ATAAGTCTTCTCACG[C/T]CTGTAATCCCAGCAC | 8945 |
rs568130565 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | BTRC | GRCh38.p7 | 10:101546905 | AGAGAAACTAAGCCT[-/A]GGCAGATCCACTGGT | 8945 |
rs568144556 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407220 | AGGCGTAGTGGTATA[C/T]ACCTGTAGTCCCATC | 8945 |
rs568183375 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | BTRC | GRCh38.p7 | 10:101497928 | AGGAGGCTGAGGCAG[G/T]AGAATTGCTTGAACC | 8945 |
rs568185274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521944 | TCCAGCTATATATCT[C/G]TCTTTAAAAGTCTTT | 8945 |
rs568195539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101462795 | ATGTCCTTGGCAAAA[A/G]CAAGAAACGCAAGTT | 8945 |
rs568205730 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530694 | TCCGATGTTCTACAC[G/T]GGAAATAATCATGTT | 8945 |
rs568208902 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101407754 | TTTGTGAGACAGTCT[C/T]GTTCTGTCGCCAGGC | 8945 |
rs568219107 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101399235 | GCTGGGATTACAGGC[A/G]TGAGCCATCATGCCT | 8945 |
rs568224101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514560 | CAGGTTCAAGTGATT[C/T]TTGTGTCTCAGCTGC | 8945 |
rs568240174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101461832 | CTTTTACATATGTGT[A/G]TATCTGTATGTATAC | 8945 |
rs568269173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396379 | CAAGATTCTGCCACT[A/G]TGCGAAAACTTGAAT | 8945 |
rs568276251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373857 | AGGGAGGTGGAGTTT[G/T]CAATGAGCCGAGATC | 8945 |
rs568277081 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101466097 | ATTGTGGCATTACAA[C/T]GTTCAACTCTTTGCT | 8945 |
rs568283584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101454873 | ACTGGGGCAGAAAAG[A/G]TGTGTTGTGGGAAAT | 8945 |
rs568286682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101540433 | GAATTGACCATATAT[A/G]TGTGAGTCTTCTTTG | 8945 |
rs568292266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413378 | GAGTGCAGTGGTGCA[A/G]TCTCGGCTCACTGCA | 8945 |
rs568292303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101404221 | ATTTTTGGTAGAGAC[A/G]GGGTTTCACCGTGTT | 8945 |
rs568319015 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407522 | GCTTCAAGTGATTCT[C/T]GTGGACTACAGGTAT | 8945 |
rs568335201 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400257 | ATCTGTGATGTGCGG[A/G]AAATCAGATGTAATA | 8945 |
rs568338594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374689 | CTAATGCTAGATGAC[A/G]AGTTAGTGGGTGCAG | 8945 |
rs568363674 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434437 | TATACATAAATTAAT[C/T]TGAAATGGATCATAG | 8945 |
rs568368770 | snp | A/T | 1.7753e-05 | 0.00297929 | intron-variant | BTRC | GRCh38.p7 | 10:101414643 | GGTCCATAGATGTTA[A/T]TTGCTCCCAAAGACC | 8945 |
rs568386156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516408 | AAACCAGGTCTTTTT[A/T]CTCCAGGGCCAAAGC | 8945 |
rs568396312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457345 | AGCCATGAAGATGTT[C/G]GTGGTGGGATGTCAG | 8945 |
rs568411863 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101532741 | AGTTTGCATTAGTAC[G/T]GAAGCTATATGTGTG | 8945 |
rs568452507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523924 | TACATTAATCTTGTA[A/G]GAATCCTAGGGGAAA | 8945 |
rs568455376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398476 | CCCAGATAATGTTTT[A/G]TATTTTTTAGTAGAG | 8945 |
rs568465099 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101552089 | TAATATTCTTCCTGA[-/CT]CTCTGATTATTTGTG | 8945 |
rs568467406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390911 | ATTAATTTTATACTT[C/T]TTAAGACTTGTAGGG | 8945 |
rs568497290 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493430 | AATTTGCCCAAGGTC[A/G]TACTGTATGTTGCAG | 8945 |
rs568501210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101465306 | ATTTAACATTGTTTT[C/T]AACTAATATTATAGT | 8945 |
rs568502609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101516923 | TTTTAAAAGACAAAG[G/T]GTGCATTTTAAAAGG | 8945 |
rs568513416 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101376515 | CACTTAGAAGAGGTA[-/T]TATCTAGTGGAAGGA | 8945 |
rs568526897 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549454 | ATGATGATGATGACA[C/G]CTGTAATCCCAGCAC | 8945 |
rs568530294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101531698 | TGCACTCCCTCCTGA[A/G]CGACAGAGCGAGACT | 8945 |
rs568585000 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101366583 | CCTTGAAGAGTAGAT[A/G]GATTTTGACAGACTT | 8945 |
rs568592627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549162 | GCATTGGGCCAGGCA[C/T]AGTGGCCCACACCTA | 8945 |
rs568606262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411649 | ATTCTTTTTTTATAC[C/T]CTACATCACTATGTT | 8945 |
rs568618932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489539 | GTGATGTAAAAAGAT[C/T]GCTTACAAAGCTTGT | 8945 |
rs568673340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376846 | ACAGACTCCCAAAGT[G/T]TATTGAATAGGCATT | 8945 |
rs568686090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101543441 | TCTCATATTCAGCAT[A/G]TAGTTGGGCCATGTT | 8945 |
rs568704641 | in-del | -/AAAAAAGA | 0.0219918 | 0.102529 | intron-variant | BTRC | GRCh38.p7 | 10:101390763 | AATTTTGTTTGTCTT[-/AAAAAAGA]AAGAAAGAAAGAAAG | 8945 |
rs568719563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101427825 | GAGCCACCACATCTG[A/G]CTCCAGGACAGTGTC | 8945 |
rs568722866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535799 | TTGTCTTAGCATTAC[A/G]TAATTGGCCAGAGAG | 8945 |
rs568740038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472450 | GTTGGGATTATAGGC[A/T]TGAGCCACCCCACCC | 8945 |
rs568755450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101362876 | GAATTAAAAACAATA[C/T]GTATAACAACTACTT | 8945 |
rs568773080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367532 | AGTGAACACATCTTC[A/G]TAACCATTATCTAGA | 8945 |
rs568776765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472851 | CTAGATACCTAACAT[C/T]CCCTTTTTCCTTGGC | 8945 |
rs568780085 | in-del | -/TTG | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101424519 | ACAGCAATCTTTTTA[-/TTG]TTGATTATTATAGCT | 8945 |
rs568788208 | snp | C/T | 0.000399281 | 0.0141238 | stop-gained, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536613 | TTGGTGCGTTGTATT[C/T]GATTTGATAACAAGA | 8945 |
rs568799840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527830 | CACACAAAAGAATAT[C/T]ATTACTACTTCTCAA | 8945 |
rs568804976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418038 | TTATCTATTATTACA[C/T]AACAAATTACCTCAA | 8945 |
rs568836843 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101491777 | TTTTGATTCATGCTT[C/T]TAGATGGTTCGGTGA | 8945 |
rs568838461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101519533 | TCCTCTTCTGTAACC[C/T]GTTGAAGCAAACTCT | 8945 |
rs568865829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101403317 | AGATGGCCAGTAAGG[C/T]CCCATAAGGACTTGG | 8945 |
rs568883062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437017 | TTACAAAACAATACC[A/G]TAAGGAAAATTATCC | 8945 |
rs568883265 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369014 | ACAGAGCGAGACTCC[A/G]TCTTAAATAATAATA | 8945 |
rs568929277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402325 | AGTAGAAATTCAAGT[A/T]AGAATAATTTACTGC | 8945 |
rs568936424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493596 | CTATTGAATGTTAAC[A/G]ATTTACTAACAACTA | 8945 |
rs568958070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452169 | AAATCTACTCCAGAA[A/G]TAGAAATCTGAGGTG | 8945 |
rs568962590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434806 | GTCTCTACTAAAAAC[A/G]CAAATTTAGTAGAGA | 8945 |
rs568980660 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447464 | CATTGGTTTCCACAA[A/G]AGGGTATTTTGGCAG | 8945 |
rs568981883 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101478269 | TTGTGCCACTGCACT[A/C]CAGCCTGGGCAGCAG | 8945 |
rs568997050 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495309 | TATAGCAGTTATAAC[C/T]ATTTTTAAGCCTCCT | 8945 |
rs569005008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434461 | ATCATAGACCTAAAT[C/T]GGAGTTAACATGTAT | 8945 |
rs569018789 | snp | C/T | 1.65323e-05 | 0.00287505 | intron-variant | BTRC | GRCh38.p7 | 10:101479365 | AACAAATTCTCTTTA[C/T]AGACATACAACAGCT | 8945 |
rs569018954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470372 | GAGTCTCGCTGTGTC[A/G]CCCAGGCTGGAGTGC | 8945 |
rs569022121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101484594 | GAGTTTTAAACTACA[G/T]GTTAACAGGCTTCTT | 8945 |
rs569040081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426627 | AGTAAACTCAGATAA[C/T]TTATCAAGTACATAC | 8945 |
rs569058054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369747 | TATTTAAAACCATGA[A/G]TTCACACTGATATCC | 8945 |
rs569136627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101486255 | CCGCATAATGTAACA[A/G]TTTCCCAATAAACTC | 8945 |
rs569138071 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461962 | TGAGAACTGAATTAA[A/G]GCTTACTTTCTTTCA | 8945 |
rs569164913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428968 | TCTTGCATGGCTCTC[A/G]TTGTCCATTTATCAA | 8945 |
rs569183204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371999 | CCAGCTTATTCAGCA[C/G]TATTTATTGAAAAGA | 8945 |
rs569189461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436097 | TATGTTTAGTTTGAG[G/T]ATATTTTTATTTTCA | 8945 |
rs569191384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445576 | TATGGATCACTGGTA[G/T]GTAATAATCGACTAT | 8945 |
rs569205793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101428140 | GTAAATGGTCGATAT[A/G]GATTGGCAGGATGAC | 8945 |
rs569237871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379241 | CTTTGATTATATGGT[A/G]GTCTTCTGAATATGG | 8945 |
rs569246861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420783 | CACTTAGCTTGATGC[C/T]TCCTTTGCCTGTACT | 8945 |
rs569257882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101368620 | GAGTAACTAGGACTA[C/T]AGGCATGTGCCACCA | 8945 |
rs569286600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101538566 | AATGCTTTAGAGACT[A/G]TATATGGAGAGAAAT | 8945 |
rs569287534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364378 | TGGTGCTATTCTTCT[A/G]TCTTTGGGACTGATA | 8945 |
rs569302888 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404570 | CTACAAGTTGAGATT[G/T]CTGTAGGATTGTGGT | 8945 |
rs569307191 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392361 | GAAACCATTGGCAAC[C/T]CCTTTGTGTTGTGGA | 8945 |
rs569369554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101521163 | TATATAGTCCCAGCT[A/G]CTCTGGAGGCTAAGG | 8945 |
rs569371035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101529988 | TACTAGCTTCCACAC[C/T]GTGTTTGGTGGGTTC | 8945 |
rs569372877 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101539483 | TCCTCTGTCACCCAG[C/G]CTATAGTGAAGTGGC | 8945 |
rs569376103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482458 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 8945 |
rs569391344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412850 | CAATAAAGTGTCTAG[A/T]TGTATTGTCTTTCCC | 8945 |
rs569403410 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411050 | GCCCAGGCTAAAGTG[C/T]ACTGGGGCAATCTCA | 8945 |
rs569410616 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101530984 | TCAAGACCAGCCTGA[A/C]CAACATGGTGAAACC | 8945 |
rs569413409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483111 | TGGTATTATGTTTGG[A/G]CCCCTATAATACCTT | 8945 |
rs569422314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473944 | AGTTCTAGAATTTCT[A/G]TTTAGTTTATTTTTG | 8945 |
rs569447462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101526566 | GGGCAGATCACTCGA[A/G]GCCAGGAGTTTGAGA | 8945 |
rs569489891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101503915 | AAGAAGAGCAGGGTA[A/G]TTTTTTCCTTCTTTA | 8945 |
rs569509127 | in-del | -/ATT | | | intron-variant | BTRC | GRCh38.p7 | 10:101418696 | AATTGGCAAACAAAA[-/ATT]ATTATTATTATTATT | 8945 |
rs569517795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101431822 | TTTTCCTTTACAAAA[A/T]TTAATATCTTAAGAT | 8945 |
rs569519198 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101394039 | CAGGGCTTTTAGTAA[G/T]TAAATGATAGATTTT | 8945 |
rs569519294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545449 | TAAAATTTATATGAT[G/T]TCTTAACCACCAGTA | 8945 |
rs569554814 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101387200 | TTCTATTTTAAAAAA[G/T]TCATATTAAAAATTT | 8945 |
rs569555528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101448585 | GGGTCTGGCTACTTA[A/G]AGACCCATGAGAATG | 8945 |
rs569576544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485512 | CCTTGAATATAGACA[C/G]AATATAGACAGCTTA | 8945 |
rs569594105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449154 | GATGGTTTTACGTCT[C/T]GGGATATTAGCTTTT | 8945 |
rs569600192 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101470304 | TCTAATAGTTGGATG[A/C]AATCCAGTTTACCAA | 8945 |
rs569602823 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101534514 | TATGTCTTAAGGACA[C/T]ACTGGCAGCATCCCA | 8945 |
rs569610295 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528608 | ATACTTATACATCCC[A/G/T]TGTCAACTTCCTCCA | 8945 |
rs569639261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432598 | TGCCTAAAAGGCTGC[C/T]CCTACTTCAGAAACT | 8945 |
rs569655271 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474198 | TAACCAACATTATAA[A/G]TGGTACATTGCAGAA | 8945 |
rs569679650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425244 | TTTACTATCGCATTG[C/T]AGCATTTCAATTTTT | 8945 |
rs569685197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392430 | ATCAGATTAAGGGAA[C/T]ACGTATCAAAAAAAA | 8945 |
rs569743956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101533783 | TTTACCATTCCAAGT[C/T]ATCCTCTGTGAATAG | 8945 |
rs569745837 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542447 | AGTTGGTTTATAATA[A/C/T]TCAGGTCTTCTGTAT | 8945 |
rs569759971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101424573 | CCAACAGGGACCTTA[A/G]TTTAGGAGATTTTGT | 8945 |
rs569765650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101368187 | AGTTCCTGCCAGAGT[C/T]GGTAGTTTAAGAGTC | 8945 |
rs569770410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101501033 | AACCCCGCCTCCACT[A/G]AAAATACAAAAAATT | 8945 |
rs569785680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457124 | ATAGAACAGTTATAA[C/T]TATACTGTAATAAAA | 8945 |
rs569788221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416528 | TGTGACTCTTCCATG[A/G]TGTCAATTGAAAGCC | 8945 |
rs569799336 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556944 | CCTCCTAACCCTTCC[C/T]CTTCTTGGACACTGA | 8945 |
rs569805331 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387148 | TATATCAGTGCCATA[C/T]TATCTTATTCATATA | 8945 |
rs569806347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398428 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 8945 |
rs569811964 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BTRC | GRCh38.p7 | 10:101509347 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 8945 |
rs569826846 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352159 | CCATCCTGTTACTGC[C/T]TTAGTCCTCTGAAAA | 8945 |
rs569829884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440068 | TGTGTATTTATAGTA[A/G]GAAAGCTCATTAGGT | 8945 |
rs569859067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385147 | AGGCTGCAGTGGGCT[A/G]TGATTCCTCCGCTGC | 8945 |
rs569878976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101506943 | TGAGTGAGCAAAATT[C/T]TCTTGCTTTGCTCCT | 8945 |
rs569911951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101360605 | TGAACTCCTGACCTC[A/G]GGTGATCCGACCGCC | 8945 |
rs569912449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101459339 | CATGGCTATTTCATC[A/G]TTACCCCTTACCCTC | 8945 |
rs569914273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101474536 | CTCCCCTTCATGTAC[A/G]TAGTTTGGGTGTTAG | 8945 |
rs569922503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361391 | GATTACAGGCATGTG[C/T]CACCGCACCTGGCCA | 8945 |
rs569952195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101390882 | ACTTTAAGGAGGTGC[A/G]TCAGTTAAGATAGAT | 8945 |
rs569971483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498885 | GTAATCCCAGCTACT[C/G]AGGAGGCTGAGGCAG | 8945 |
rs569982572 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353890 | GCAACTTATCTAAAT[C/G]TGGCTTGTGGGCAAC | 8945 |
rs569997448 | snp | A/C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355955 | TAGAAGTAAGTGAAA[A/C/G]TTACTACACTTAAGT | 8945 |
rs570001322 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527440 | CAAAAAAACTAGGCA[A/G]TTTTTAGGCTGTGTA | 8945 |
rs570008325 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380001 | TCTGTTTGCTGAATG[C/G]ACTAGTTATAACTTC | 8945 |
rs570008847 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382143 | ACCTGCCACCACGCC[A/C/T]GGTTAATTTTTGTAT | 8945 |
rs570011575 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101474783 | ACATAAACACACATC[C/T]CACCCAGTGTGGTTC | 8945 |
rs570014596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391354 | ATCTTTGGAAGTAGA[G/T]ATCTAATTTACCAGC | 8945 |
rs570033465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101393092 | CCACCTCATACCCTC[A/G]TGGGAGGAAGGAATG | 8945 |
rs570043146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509216 | ATCCTATTTCCTCTC[A/G]ATTCAAGCATGACAG | 8945 |
rs570110442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441829 | GAGATAGCAGTCAGC[C/T]GAGATCACACCCACT | 8945 |
rs570115149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524999 | TAAGTTTGTGCCTAC[A/G]GGAGTGAGAGTATGA | 8945 |
rs570143662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101368835 | TCTAGCCTGGCTAAC[A/G]TGGTGAAACCTCGCT | 8945 |
rs570149173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101442702 | ACATAAACGTAAAAA[A/G]GAATTAACGTTTTTG | 8945 |
rs570153467 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101480292 | TATTATTAGAGCTTA[G/T]GACTGGTGTCATGTC | 8945 |
rs570187720 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481074 | ACATGAGTGCATGCC[A/G]CCACACCCAGCTAAT | 8945 |
rs570198067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396179 | TAAAAAAACACACTG[C/T]CTTTGCTCTCATTTC | 8945 |
rs570200087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387921 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCTGCCT | 8945 |
rs570202266 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469958 | TTGAATAAATATATC[A/G]CAGTTTGTTTTCTGT | 8945 |
rs570259838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101388793 | ACTGCACCCAGCCCA[A/G]CCTGTTTTATTCTTA | 8945 |
rs570263598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101461016 | CAGGCGATTCTCCTG[C/T]CTCAGACTCTCGAGT | 8945 |
rs570264739 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446470 | TACCTGGCTTCTATT[C/T]GGTTGTAATTGTGAC | 8945 |
rs570266984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101466846 | CTTTTCTACCATATT[C/G]CCCTCCCCTGAAAAA | 8945 |
rs570267716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363750 | ATATTAGATCTTGAT[A/G]AATAGATAGATTTTG | 8945 |
rs570273576 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101448917 | AAATTTATAGAAATA[A/C]GTGAGAGGAATGGTA | 8945 |
rs570280549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417171 | ATTATTTTGTCATCT[A/C]ATCCACAGATCCCAT | 8945 |
rs570317588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101517944 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 8945 |
rs570320982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101418729 | TTTTTATTCTGGGGT[A/G]CATGTGCAGGATGTG | 8945 |
rs570331479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356366 | ATGTGATTTACAGAT[C/G]ATAAAGAGACATTAT | 8945 |
rs570335198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101400544 | TAAGTCTAATGCTAA[A/G]GATTTGCCTCCTCTC | 8945 |
rs570350376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458792 | AGTGATGTGCTGTTT[C/T]CAGTACATCATATTA | 8945 |
rs570360251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101408980 | CTTGAACCGGGGAGA[C/T]GGAGGTTGCAGTGAA | 8945 |
rs570395346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498649 | AAAGTTTAGTGGGCA[C/T]GTCCTAATACAGCCT | 8945 |
rs570401832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101404778 | CCGAGGTGGGCGGAT[C/T]ACGAGGTCAGGAGAT | 8945 |
rs570404695 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | BTRC | GRCh38.p7 | 10:101505634 | CAAAAAAATAAAAAA[A/T]AAAAAATAATAATAA | 8945 |
rs570414376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453919 | CCACTTACCTCTTCC[A/G]TTGTAGTGTGAAAGC | 8945 |
rs570440030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101504657 | TGCGTTCCTCCTTCT[A/G]CTTTCCCATTTTCCC | 8945 |
rs570443545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101356926 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 8945 |
rs570451624 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101492428 | CTTGTGGATTAATGG[A/G]CAACCTAAAGAGTGC | 8945 |
rs570457516 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501120 | ATTGCCTGAACCTGC[A/G]GGGCAGAGGTTGCAG | 8945 |
rs570463632 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555321 | GTTGAATGTTTATTG[A/G]TGCCCAGGGTTTTGC | 8945 |
rs570471464 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101470329 | TACCAATTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 8945 |
rs570503838 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101445774 | CCAGCAGAATTCCCC[A/C/T]GAGGCCTTGGACTCT | 8945 |
rs570507205 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101544409 | TTTACTTGGGAAAGT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs570542609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101446663 | CCAGGAAAGATTGCA[A/G]TATTCAACACCATCA | 8945 |
rs570545258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101414430 | AAAAAAGTGTAGTAC[A/G]TACTATTATGTACAG | 8945 |
rs570579110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470271 | TTGCCTGTTTATGGT[A/G]TGTTTTGATGAGAAG | 8945 |
rs570579179 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407634 | GAGCTCAGGCAATCC[G/T]CCCACCTTGGCCTCC | 8945 |
rs570580172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101371926 | GGCTGAAAACCCAAT[C/T]GTCATGCTTACAAAC | 8945 |
rs570583536 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101384831 | AAAAGATAGGAAGAT[-/C]AACTGAGGACAAGAC | 8945 |
rs570593638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528937 | CTAGATGGATTTGAC[A/T]GTCTTCCCCTGGGAC | 8945 |
rs570606468 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412842 | TATACAGACAATAAA[A/G]TGTCTAGTTGTATTG | 8945 |
rs570614183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101469424 | CCCTCAGGCCTGGCA[C/T]AGAGTTTCTGAATCT | 8945 |
rs570661145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411924 | GATGCTCTTGTGGCT[A/G]ATTTTAAGCTTTATT | 8945 |
rs570663663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547421 | TCTCGGCTCACTGCA[A/G]CCTCCACCTCCTGGG | 8945 |
rs570674141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101420506 | AACCCTCACTGCCAT[A/C]CCCCCACCCTCCACT | 8945 |
rs570703235 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101375787 | ACAGATTCTTAGTTC[-/T]TTTTCCCCCCTCTTC | 8945 |
rs570713993 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442350 | AACCTTAACGGGAGA[C/G]ACTATGAGAGACATG | 8945 |
rs570746492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548308 | TGTTTTATAATAGCC[A/G]TAAACTATAATCAGC | 8945 |
rs570746837 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385931 | TTTTAATAAGGGTCT[G/T]ACTGTAAAACTTGAG | 8945 |
rs570750802 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101539737 | GTATGTTTAAAATTT[G/T]TAGAAACTGCCAAAC | 8945 |
rs570787188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101540339 | GTTGGGCTTTTTTAC[A/G]CATGAATATCCAGTT | 8945 |
rs570830260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532655 | TCTTCTTGAAATGCA[C/T]TGAATGGGCTGTTAC | 8945 |
rs570852053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406332 | CAGGCGCCCGCCACT[A/G]CGCCCGGCTAACATT | 8945 |
rs570853618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101366417 | AATATCTCTTAAGGC[A/G]CACTTTGTTAAGTGC | 8945 |
rs570892150 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101467727 | GAGATGTTTATTAAT[-/A]AAAAAAAATCACAAT | 8945 |
rs570905769 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539302 | TAGTTGGAGCAACAG[A/G]GTGGACAGACACCAC | 8945 |
rs570915260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101380521 | ACTTCCCAGACGGTG[A/G]GGCGGCTGGGCAGAG | 8945 |
rs570925396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438059 | AGTATTCATTTTCGT[A/G]CTTGATTCTTTAACA | 8945 |
rs570938277 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101464534 | TAATTTAACAACCTT[C/T]CCCCCCACCCCCCCC | 8945 |
rs570978633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101372786 | GAGAATCGCTTGAAC[C/G]TGGGAGGCAGAGGTT | 8945 |
rs570988016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359438 | ATTTTCTTTTTTTTT[A/G]TCTGAGATACCCTGA | 8945 |
rs570997693 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556105 | TCTTTTTGGATCTCT[A/G]TTGACAAGTAATAAA | 8945 |
rs571020565 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101474822 | CAAGATCAGGCCACT[C/T]CTTCCCCATTTTCCG | 8945 |
rs571032956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487072 | AAATAATTTTGATTC[A/C]TAAGTAATAAAATTT | 8945 |
rs571133807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479533 | GCATCTTTACTCAGT[A/G]TTGCTTAAGGATTAT | 8945 |
rs571141279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551659 | GTGTGCCTCAGTTCT[C/T]GTGGCGGAAGTACAT | 8945 |
rs571151628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101542631 | GGCTGGAATGCAGTG[A/G]CACACCCATGACTCA | 8945 |
rs571160725 | snp | G/T | 1.65836e-05 | 0.0028795 | intron-variant | BTRC | GRCh38.p7 | 10:101536493 | GTTATAACATTCCAG[G/T]CTTAGAAAAGAATAC | 8945 |
rs571162122 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476883 | TATAGCAATGGTTCT[C/T]GAAGAGTGTTCCTGG | 8945 |
rs571172489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101480367 | CATGTGAGCTGCTAT[A/G]ACAAAAATACTGTAA | 8945 |
rs571182810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101476090 | TGAGAGGGGCACATC[A/G]CCTCTAAAGTATCTT | 8945 |
rs571191123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535776 | CCTTACTAGAAATTA[C/T]GTAATTTTTGTCTTA | 8945 |
rs571193815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101365422 | CACTCTGTCACCCAG[C/G]CTGGGTGATATTTCT | 8945 |
rs571198404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101425485 | GCTGGATTTGTGTAG[C/G]ATGCAGTCATTATCT | 8945 |
rs571214379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369633 | GTGTTAAGCGTGCTC[A/G]TTGCTATTGGGGTGT | 8945 |
rs571225833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526807 | GTGGAATAAGAACTC[C/T]AGCCATCAGAAAAAG | 8945 |
rs571232783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426445 | TTTTGGAAATCACAC[C/T]GGTATATCTAGTGGC | 8945 |
rs571245458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527573 | GGCTGGGCAACATAT[G/T]GAGACCTCATCTCTA | 8945 |
rs571248585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467489 | AGACACTTCTCCCTC[C/T]AGTGGCAATAGTAAG | 8945 |
rs571258606 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101420804 | TGCCTGTACTCACCT[A/G]TTGAACTGTTCAGGT | 8945 |
rs571265745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410858 | TACATTCCTATCCTT[C/T]GTGTTATTATTGTCA | 8945 |
rs571267734 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101418516 | TAATACTTATTTTCA[A/G]TAAATTTTTATGAGC | 8945 |
rs571269864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468437 | GTTGTGCTCATCTGC[A/G]TGAGCCCTAAAAAAA | 8945 |
rs571275939 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364768 | GGTATTCTGAAAATA[C/T]ACTAGTAAATACACA | 8945 |
rs571280443 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101362203 | TCCTTGTGATTCGCC[C/T]GCCTTGGCCTCCCAA | 8945 |
rs571290887 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101447923 | ATTATTAATATTTCC[-/A]AAAAAAACCAATTTC | 8945 |
rs571318853 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101410105 | TGGGTTTTCTTGTTT[C/T]AATTGTAACGTCAAA | 8945 |
rs571332461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401579 | TATCTTACTCTTTCA[C/G]ATTCAACAATCTTAT | 8945 |
rs571332925 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387821 | CAGCCTCCTGAGTAG[C/T]TGGGATTACAGGTGT | 8945 |
rs571342017 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424414 | ATTACATGATTATGG[C/T]ATACTGCATTTCTCT | 8945 |
rs571352985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101354657 | TGGGGAAGGGAGCGC[A/G]GGATAGAGTGAAGAC | 8945 |
rs571356891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518612 | ATTAGTTACCACCAC[C/T]GGAATGACCAGGATG | 8945 |
rs571384754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441672 | ATTGCCTGAGCTCAC[A/G]AATTTGAGACCAGCC | 8945 |
rs571392717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510266 | GTAATCCCAGCACTT[C/T]AGGAGGCAGAGGTGG | 8945 |
rs571394467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362709 | CAGAAGAAATTTTTT[A/G]TGTTTTGTTAATACA | 8945 |
rs571394541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101519456 | ATTTTCTTACTGGCT[C/G]TCAGCTGGGGGCTCC | 8945 |
rs571404613 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404167 | TCTCGAGTAGCTGGG[A/G]CTACAGGTGCCCGCC | 8945 |
rs571420923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433465 | TGAATAGGAATTAAC[C/T]CGATAACAGGGAGGA | 8945 |
rs571427833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101384783 | GAGAAGTAAAATACA[G/T]TGTAGTTAAAAATTG | 8945 |
rs571438212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434430 | TGCACTATATACATA[A/T]ATTAATTTGAAATGG | 8945 |
rs571493017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101376767 | AGGTGCTTTGTAGGT[C/T]ATAGGGTAAGGTGGT | 8945 |
rs571496818 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101376077 | ACGCCTGTAATCCTA[C/G]CACTTCGGGAGGCTG | 8945 |
rs571519700 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484618 | GCTTCTTTAAGATAC[G/T]GTTCCACAAGTAGCA | 8945 |
rs571540576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483298 | AGGCCTAAGAAAAAA[A/T]TTAAAACTAAAAATG | 8945 |
rs571545401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451996 | CACGAGTTCATAAAT[C/G]AAAGGAGTTTGTCAA | 8945 |
rs571546107 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101426185 | GAGTAAAAGTTATAG[-/C]CCACTCCATTTATTT | 8945 |
rs571555607 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101509833 | TCCCAAAATTCTGGG[A/G]TTACAGGCATGAGCC | 8945 |
rs571576039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101377421 | ATGAGGGAGAATTGC[A/G]TGATAAATGTAGGTT | 8945 |
rs571576808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483738 | ATGAGATTTGTGTTT[A/G]GAGCATGATGAGCTC | 8945 |
rs571580664 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532186 | TTTTCCCTAAGTTGT[A/G]TATATCCCATAGAGT | 8945 |
rs571606222 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101546186 | ACATTCTTCTCAAGC[A/T]CCCAAGGAAATTACA | 8945 |
rs571612529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101368949 | GCTTGAACCTGGGAG[A/G]CGGAGGTTGCAGTGA | 8945 |
rs571620934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101544604 | AGAGATAGGGTCTCA[C/T]TGTGTTGCCCAGACT | 8945 |
rs571629517 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101378548 | TTTTTTTTTTGAGAC[A/G]AAGTCTCACTCTGTC | 8945 |
rs571633398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101387119 | GACTCATTCTGTTCT[A/G]TTGTTCATTTATTTA | 8945 |
rs571673616 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101373158 | TAAATCTGTGGTCTG[C/T]GGCCCCTGTACAAGC | 8945 |
rs571714011 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487325 | GTCAAAACCAACTAT[A/G]TGAAGAACAGGATTT | 8945 |
rs571748995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546136 | TGGATATAATTGACA[A/G]CTATAGAATGCTTCA | 8945 |
rs571788488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522609 | TATTTTTAGTAGAGG[C/T]GGGGTTTCACCATAT | 8945 |
rs571796238 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101428874 | TCTTGCTGTGCTGCC[C/T]AGGCTGGATTTGAAC | 8945 |
rs571807924 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366415 | TAAATATCTCTTAAG[A/G]CGCACTTTGTTAAGT | 8945 |
rs571833488 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101551279 | GACCTTTCAAGCCAA[G/T]TAAACAGTCTGATGT | 8945 |
rs571862148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502390 | TCTGAAAGATTGAAA[A/G]TGAAAAAAAAAAATC | 8945 |
rs571862549 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397732 | TTTTTCATACCCTGT[C/T]ACTGTATCATTTTAG | 8945 |
rs571863179 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101503253 | TATGTAAACCTCTTT[C/T]GGTTATAGAAATGCA | 8945 |
rs571868910 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101417142 | ATCAGAATTAAGGAA[A/C]TTATTATTGGCATAT | 8945 |
rs571885467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511052 | TTGTAAGGCACAAAT[C/T]AGACAATGCCATATG | 8945 |
rs571890737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101443858 | CACAACTAGCCACAA[C/G]TCCGATTCGATTCAC | 8945 |
rs571923784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101479755 | AGATAATGTACAATT[A/G]TTTTGATAAGTTTAT | 8945 |
rs571933274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101496062 | TGAGAGTCATTTATA[C/T]TGTTATGTATGTATA | 8945 |
rs571947694 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101493766 | AAAACGCCTCAATTA[C/G]CAGCCACAAAAAAGT | 8945 |
rs571971943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101496946 | CTTAATTTAAGAGTC[C/G]AATTTATGGATCTTT | 8945 |
rs571972046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101486781 | CATTTTCTTTACAAC[A/G]TGAAATATATATTCT | 8945 |
rs571979627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552184 | ATTTTATTTCATTTT[A/T]TTTTATTTTATTTTA | 8945 |
rs572009144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101471734 | TGAAAGATTTTTTAA[A/G]CTTATTATTTAAATT | 8945 |
rs572012899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101372270 | TTTCTTTTTCTTTTT[C/T]TTTTTAAATGGAGTT | 8945 |
rs572057697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487400 | ACTTGCAGACTTAAA[C/T]ATTTCCTTTTGCTGA | 8945 |
rs572071840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101422326 | TGGGGTTGTTTGTTT[C/T]TTTCTTGTAAATTTG | 8945 |
rs572084090 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101512056 | CCTCTTCAGAGAAGG[A/C]AAAGACACTTTGTAT | 8945 |
rs572088800 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101358409 | TGCCAAGCCACGTTT[A/G]TTTTTAAAAACAGGA | 8945 |
rs572096972 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101446073 | AGCCTGGAGAAAAAA[C/T]TCAGCATTTAAGTAC | 8945 |
rs572109409 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101472548 | GCTGGGCGTGGTGGC[C/T]CATGCCTATAATCCC | 8945 |
rs572157869 | in-del | -/CAGCTTTGTAGAAGAAAGCTTCATAT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101363713 | TGAAGAGCTCTTTAG[-/CAGCTTTGTAGAAGAAAGCTTCATAT]TAGATCTTGATGAAT | 8945 |
rs572159560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423280 | GGGAAGAGCTTGTTC[C/T]GCAATTCATTGCCAA | 8945 |
rs572173883 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101463435 | TCTGCCCAGCTTGGC[C/T]TCCCAAAGTGCTGGG | 8945 |
rs572185289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437754 | CTCCCTCTCATGTAA[C/T]TGTTAGTCATTTCAA | 8945 |
rs572216378 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | BTRC | GRCh38.p7 | 10:101550293 | ATTTATTTTTATTTT[A/T]TTTTTTTTTTAGACA | 8945 |
rs572227569 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101505779 | CTACTGTAAATGCTA[A/T]TTTTAGAAAATGAAT | 8945 |
rs572253961 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554469 | ATCTCTCAAATATTG[A/G]TCTCACCGTGTCAAC | 8945 |
rs572271856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101523100 | TCTCAGCTACTTGGG[A/G]GACTGGGGCAGGAGA | 8945 |
rs572279644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438208 | AAGGAGGGCAGATCA[C/G]AAAGTCAGGAGATTG | 8945 |
rs572293883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101389111 | CATAATTGTGATTTT[G/T]TGTGTGTGTTTTTTT | 8945 |
rs572305858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439425 | CCACTCTGATTGCTG[C/T]TCCCTTTGGCATTAC | 8945 |
rs572306845 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101515872 | CTACAAATTGTATAG[C/G]TGGATGGTTTTCAAA | 8945 |
rs572308437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101380843 | TAAGTGGTTGTGTGA[A/G]CTTCACAGAGTGTAC | 8945 |
rs572320184 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101381706 | CGATGATAACTCATA[G/T]ATCCCTCACCTGAAT | 8945 |
rs572324839 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424170 | ACCTGGGAGGCGGAG[G/T]TTGCAGTGAGCCGAG | 8945 |
rs572348398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429325 | AAAGCTGTAGCTGCA[A/G]TAATACTAATGTCAG | 8945 |
rs572361736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101448830 | TTTTTTTTTCTCCCT[A/G]TATATTACTTTTCTT | 8945 |
rs572370004 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443118 | GGATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 8945 |
rs572387407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547707 | ATTTTAAAATGTAAT[A/G]ATGTGCCAATAAAAT | 8945 |
rs572396328 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101516506 | GTCTTTCTGCCTCAT[C/T]AAAAAAATACTCGTT | 8945 |
rs572404083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101397950 | TTTAAAAATGCCATT[A/G]TTTCCTTCCCAAATT | 8945 |
rs572418274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498644 | GTTTTAAAGTTTAGT[A/G]GGCACGTCCTAATAC | 8945 |
rs572423858 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101504245 | CGCCTGAAACATTAA[A/G]TAGTGGTTTTAAAAA | 8945 |
rs572426885 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556723 | CATGATGATGGCTGC[C/T]TGGTTTCAGGTGGAA | 8945 |
rs572446667 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101417028 | TTTTTTTCATAAACC[A/G]CTTGAGAATAAGGTT | 8945 |
rs572458871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101446840 | TCTTATGTTTCTTCC[C/T]TCTATCCCCCAAAGA | 8945 |
rs572463086 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101541474 | ATCATGTTAGCCAGG[A/T]TGGTCTCGATCTCCT | 8945 |
rs572485764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382309 | CTTTTACAGCTCTTT[A/T]AAAAAAAATCCAGGA | 8945 |
rs572487846 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | BTRC | GRCh38.p7 | 10:101473392 | TGGGCTCAAGCAACC[A/G]CCCACCCCAGCCTCC | 8945 |
rs572489985 | in-del | -/AGAC | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101471396 | ACTATCTCCAAAAAT[-/AGAC]AGACAGATAGATAAC | 8945 |
rs572503735 | in-del | -/AG | | | intron-variant | BTRC | GRCh38.p7 | 10:101415012 | CTAGCCTAAGTGCAC[-/AG]AGTTTATTGGCCATC | 8945 |
rs572523028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490343 | TACATTAAAATGTAT[G/T]CAGCCCCAGTGTTCA | 8945 |
rs572531406 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101394020 | AGTCTGTACCTAGGA[C/G]TTCCAGGGCTTTTAG | 8945 |
rs572547715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101375016 | GCTAGGAGTTGGGGA[A/G]AAGAAATTGACTAGG | 8945 |
rs572555276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358998 | TAAAAATGGTATCGG[C/G]CAAGTTTGTGGGTCA | 8945 |
rs572609420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101482170 | GATTACAGAAGTGTG[G/T]CACCACACCCAGCTA | 8945 |
rs572621397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101490834 | GAGGCCTAGGTGGGC[A/G]GATCACTTGAGGTCA | 8945 |
rs572637548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406628 | CACCTCCACCTCCTG[G/T]GTTCAAGTGATTCTC | 8945 |
rs572639548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506622 | AAGATGCCAACTCTG[C/T]CATAGTTAAATGTTA | 8945 |
rs572665252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101463959 | GCTTTAAAAAAAAAA[A/C]CAAACAAAAATCCAC | 8945 |
rs572667925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447955 | GCTAAATGATAGTAA[A/T]ATTTTCTATAATTCA | 8945 |
rs572673135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101527132 | ATAATAGGCATGTGT[C/G]TGCTTAGTGATGTCC | 8945 |
rs572676127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498085 | AGTGATTTTGTGTGA[C/T]ATATACACACAAAAA | 8945 |
rs572690481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101370937 | ATATGTACCTATATA[C/T]ATACACACACATATA | 8945 |
rs572703856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452224 | TTAATCAGTTTCTGC[A/C]TACTAGCATAAATGC | 8945 |
rs572705609 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510823 | CCTTTGGTTTCTCCT[C/T]CTTCATCCTCTGTCA | 8945 |
rs572715778 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101388781 | CAGGCATGAGCGACT[A/G]CACCCAGCCCAGCCT | 8945 |
rs572727036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507157 | TCACTGGGGCTTTTT[C/T]CCCATTTTTTCCCAT | 8945 |
rs572729212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541540 | GCTGGGATTACAGGC[A/G]TGAACCACCGCGCCC | 8945 |
rs572739951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410174 | CTTCTAGTACATCTG[A/G]ATTTCCTGGTATGCT | 8945 |
rs572749636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101443143 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACG | 8945 |
rs572752605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401827 | TGGGTGACAGAGCGA[C/G]ACCTCATCTCAAAAA | 8945 |
rs572790077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101444227 | GTGATGTTTGTGATA[A/G]CTGTACATGTAGCTT | 8945 |
rs572816359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101402449 | TGAATATAATTTATT[A/T]TAGAAGGCACCCAAA | 8945 |
rs572891546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101461368 | ACTCATTTTCAGTTG[A/G]ATTGTTGTTTTTTTC | 8945 |
rs572906819 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101410423 | AGTTGGAGACCAGCC[C/T]GGCCAACATGGTGAA | 8945 |
rs572913048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544780 | TAATTCTATATAGGC[C/T]AGGCATGGTGTCTCA | 8945 |
rs572926723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453525 | CTGTTGCACCATCCA[A/C]CCTTGAGCAAGATGC | 8945 |
rs572930830 | snp | C/G | 1.65042e-05 | 0.0028726 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101461994 | AGAATTCCTCAGAGA[C/G]AGAAGACTGTAATAA | 8945 |
rs572935253 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514044 | GTTGAACATCTTTTC[A/G]TATGCTTATTGGCAT | 8945 |
rs572950244 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450658 | AGTTGTTCAGTTTTC[C/T]ATTATTTTAGCTTTG | 8945 |
rs572952020 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485155 | TGGTCTGTGTTAAAG[G/T]TGGTAAAATTTAAAC | 8945 |
rs572953488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354239 | TTATGGTGAGGAGAC[C/G]GTGGAGGCCGGGGAA | 8945 |
rs572975291 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101354882 | AGAAGATAAGGACTG[C/G]GAATGAGGACCTAGG | 8945 |
rs572980051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377740 | CTATGAAAGACTTCA[A/T]TAATATTTTTAAAAA | 8945 |
rs573013087 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483164 | TATCATAGTCTTATG[A/G]TAGCTCTATACGAAG | 8945 |
rs573022989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495088 | AAAACTTTCTATTTT[C/T]CTCTACCAAAGAGCA | 8945 |
rs573043017 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101396484 | CGAGGTAAAGATTTT[-/A]AATGGAGTTCAGCTA | 8945 |
rs573055189 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101422780 | GATCAGATAGTTGTA[A/G]ATGTGTGTTATTATT | 8945 |
rs573064355 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101427640 | TCAAGCAGTCCTCCC[A/C]TCTCAGCCTCCCCAA | 8945 |
rs573066381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101436367 | TATAAGTAAGGGGCC[A/G]GGCACGGTGATGCAC | 8945 |
rs573081277 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425070 | GGTTTTCTGTTTCTG[C/T]ATTAGTTCGCTTAGG | 8945 |
rs573090288 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101511461 | GTTGCCCAGGCGTTC[A/G/T]AGCAGTTCTCGTGCC | 8945 |
rs573135800 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431639 | CTTTTAACCTGTTGT[C/T]CATATCTATTTAGAA | 8945 |
rs573182843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101470479 | ATGGGATTACAGGCA[C/T]GCGCCACCACATGCT | 8945 |
rs573191552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101460610 | CCTGTCAGGCTTACT[A/G]AAGGTGACACACAGG | 8945 |
rs573205487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357050 | AGGAGAATGGCGTGA[A/G]CCCGGGAGGTGGAGC | 8945 |
rs573227921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101412912 | TAGATAATCAAAAGT[A/G]GAAATTGGCCAACAG | 8945 |
rs573244896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530098 | ATCTAGCTTGGGATA[C/T]GAGTATTCCAGAGAT | 8945 |
rs573254065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101513565 | TGGCTTCTTTGATTC[A/T]GCATGTTTTTGAGGT | 8945 |
rs573292355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101504944 | ATAAATTTTAAAAAA[A/T]TTTTGTTTTCTTTTT | 8945 |
rs573292894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464955 | CAATAGAAGCGGGTC[A/G]CAGGGCAGCTGTCCA | 8945 |
rs573295104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101474118 | GTTGGTTTTTGGTTC[A/G]TTTTTCTCTTGACAA | 8945 |
rs573312671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101545561 | AATCCAATATGACTG[A/G]TGTCCTTAAAACAAG | 8945 |
rs573325572 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352857 | GAGTAGCTTGAATTA[C/T]AGGCGCGTGCCACCA | 8945 |
rs573354613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378843 | TTGTTTCCATGGGAA[A/G]ACATCCGCTTTGAAG | 8945 |
rs573369770 | in-del | -/CTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101517753 | TGGGTGTGATTTTGT[-/CTC]CTTTTTTCTCATACT | 8945 |
rs573372138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101395015 | TCTCACATGATTCCA[A/G]CAGCAGTAGCGCCTA | 8945 |
rs573422841 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101477729 | ATCTCAGCTCACTAC[A/T]ACCTCCATCTCCTGG | 8945 |
rs573445687 | in-del | -/GTGT | 0.0142736 | 0.0832652 | intron-variant | BTRC | GRCh38.p7 | 10:101431028 | GAGACACTCTAGCTA[-/GTGT]GTGTTTCATGAATTA | 8945 |
rs573461139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363341 | AGAGCAGGAAAACTG[G/T]GGGATATGGTGGCAT | 8945 |
rs573463924 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101440263 | AGTTTATAAATTACA[A/G]TACATCTTAAAACAA | 8945 |
rs573483398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412152 | GTTGTGGAATTTCAC[C/T]GTATGTATACAGGAC | 8945 |
rs573494512 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553671 | CTTAGGAGGAGACAG[A/C]GTTCCCTCTGTATAG | 8945 |
rs573532324 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101359997 | ATTCAACTTTGAGTA[C/G]TTTTAGAAATTATTT | 8945 |
rs573568003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101360749 | TGATCTTTGTGCCTC[A/G]GCCTCTCCAGTAGCT | 8945 |
rs573595737 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101416681 | TAGTTTTTCAGCATC[G/T]TACTCTCTGCGTGTA | 8945 |
rs573603660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101473205 | GATTTCAGTTTATCT[A/G]TCTTTTTTTTTTTCG | 8945 |
rs573648208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524307 | GTCTGTGTGTACCTC[A/G]TTACTTTGTTCTCCC | 8945 |
rs573663130 | snp | A/G | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101376240 | TGAGGCCAGAGAATC[A/G]CTTGAAACCAGGAGG | 8945 |
rs573667825 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101479064 | AACTGCTGTTTTAAA[C/T]AGAACTAAGCTCTTC | 8945 |
rs573674290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101517224 | ACCAGGATTACAGGT[A/G]TCAGCTCCTTCTGTG | 8945 |
rs573686935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525114 | CAGTTGTAAATGTAG[A/G]ACAGCAGGCAAAAGA | 8945 |
rs573695718 | snp | G/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352493 | GGTTATATAGATGAA[G/T]TATAGTGGTGAAGTC | 8945 |
rs573696838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458295 | ATAATTCCATTTATA[G/T]GACATTCTGAAAATG | 8945 |
rs573729669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101399043 | CTGCAACGTCCGCCT[C/T]CTGGGCTCAAGCGAT | 8945 |
rs573730043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101408167 | AAGTGCTCAGTAGCC[A/G]TATGTGACTAGTGGT | 8945 |
rs573730932 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393595 | TCATGATTCCAACAG[C/T]ATTTCAGTCTTGGGG | 8945 |
rs573734305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481134 | TGTTTTGTAGAGATG[A/T]GGTGTCGCTGTATTG | 8945 |
rs573743046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101535282 | GTTTTCTGCTTCTCT[A/G]AGACTCCATTTGCCA | 8945 |
rs573748015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101549481 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 8945 |
rs573761971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101489990 | TGGAGAAATTTTCAT[G/T]AGTCTAGTCCTTTGG | 8945 |
rs573767546 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101510124 | AGGTGACAGGCAAGA[A/C]TCTGTCTCAAAAAAA | 8945 |
rs573773358 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | BTRC | GRCh38.p7 | 10:101369219 | TATTGGAGTATTATT[A/T]TTTTTTTTTTTTTAA | 8945 |
rs573825030 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543560 | ATTTAAATCTATCAT[A/G]TTGCTATTTATTTTC | 8945 |
rs573825471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101541436 | GGCTGATTTTTTGTA[C/T]TTTTTAGTAGAGACG | 8945 |
rs573831774 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101367110 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8945 |
rs573834557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369874 | ATATTTTCTTAGTCA[A/G]TCAGCCCCTTTCTAT | 8945 |
rs573843275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101374211 | CTATTTCTCCACATC[C/T]TCTCCAGCACTTGTT | 8945 |
rs573845205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101382272 | ACAGGCATGAGCCAC[C/T]GCGTCCGGCCCCTAA | 8945 |
rs573860145 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450036 | GTAAGGTAGGAAGTG[-/T]TTTTTTTTTGTTTGT | 8945 |
rs573916016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367812 | TTAATGTATTCCACT[C/G]TGATTAATCATTCAG | 8945 |
rs573935650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542809 | GGAACTCCTGGGCTC[A/G]ACCTCGACAAAGTAC | 8945 |
rs573956984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101491260 | TGACTTACTTTAGTA[A/G]TTGTTTTAGAAGTTG | 8945 |
rs573960843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101374927 | TCATAACCGCTGTCT[A/G]TTGGGAACACAGTTT | 8945 |
rs573961940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101483397 | CAGGAGTTCAAGACC[A/G]GCCCAACCAACATGG | 8945 |
rs573967015 | snp | A/T | 0.000396059 | 0.0140667 | intron-variant | BTRC | GRCh38.p7 | 10:101532938 | GATCAAAAGGATCTT[A/T]TTTGCCATCCTAGAT | 8945 |
rs573991030 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553872 | CCTCTCACATGAGCC[A/G]GATCAGCCAGAAAAT | 8945 |
rs574039139 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101517030 | GCCTGCCTGTGTGTT[A/C]GTTCTCTAAATCTTC | 8945 |
rs574041054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492085 | AGAAACACTTGCTCA[A/G]CATGGAGCACTAAGA | 8945 |
rs574044417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101433838 | AAGAGAGAGATGATG[A/G]CAGCTTGGTTTTGGA | 8945 |
rs574046027 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101474792 | CACATCTCACCCAGT[G/T]TGGTTCTCTTCTTTC | 8945 |
rs574066624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417387 | AACATTTTTCAAATT[G/T]GGTTTTTCTGATGTA | 8945 |
rs574119096 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101362036 | CATGATCTCAGCTCA[C/G]TGCAACCCCCGACTC | 8945 |
rs574131051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449520 | TGGATGAAATATTTT[C/T]GTAAATATGGCAGCA | 8945 |
rs574134777 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549655 | GGAGGCAGAGCTTGC[A/G]GTGAGCTGAGATGGC | 8945 |
rs574168943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101426743 | TCACAAAAATAAATA[C/T]GTATATTTTAATTTT | 8945 |
rs574171306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101509496 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 8945 |
rs574172040 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547290 | GGTGACAAGAACGAA[A/G]CTCCATCTCAAAATA | 8945 |
rs574172772 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101372192 | TGATAGTATATGCCC[C/G/T]TCAGCTTCCCCTTCC | 8945 |
rs574173309 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547378 | GTCTCACTCTTGTTA[C/T]CCAGGCTGGAGTAGT | 8945 |
rs574178956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101539807 | TAGCAGTGTATGAGA[A/G]TTCCAGTTACTCCAC | 8945 |
rs574185839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101450067 | TTTTAAATTAAGGCT[A/T]TAGAGCCAAAAAAAA | 8945 |
rs574222900 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510025 | ACAAAAATTAGCTGC[A/G]CGTGGTGTTACATGT | 8945 |
rs574232520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373047 | TCTGTTTAGAGGTCT[C/T]TATATATCTTTTGTT | 8945 |
rs574244014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101392481 | ACTAAAAATTAATTG[A/G]AAGTTTTTTGTTGTT | 8945 |
rs574251896 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101384321 | TGACCTTAATATTTG[C/T]TTCCCAGGCTAAATC | 8945 |
rs574323809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101441361 | GCTTTATTATTTAAA[C/T]TCCAGGCTTGCCTCA | 8945 |
rs574329517 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452895 | CTTTAGGTCCTCCCT[A/G]AAATGAGTCCTTGAA | 8945 |
rs574342105 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458423 | TCATTTTTTAATGGC[A/G]GTGTTATACAACTGT | 8945 |
rs574349022 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101495278 | CCATGAATAAATATT[A/C]TGAATTATCTAATAT | 8945 |
rs574396906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429248 | AAATTTCATCCTGGG[A/T]TACTTTTAGAGAAAC | 8945 |
rs574408052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101442036 | AGGAACTTAGCCTGG[A/G]TTTGTTTCCTCATCT | 8945 |
rs574417262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101478844 | TGTGGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA | 8945 |
rs574421498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101547515 | TCAGCTGATCTTTGT[A/G]TTTTTAGTAGAGACT | 8945 |
rs574444041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101487185 | TAGGGTTTCTTGTTA[C/T]ATAAGGTATAGGAGG | 8945 |
rs574446837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437564 | TTAAATGTCCTCCCA[G/T]AGATTACCGTTTCAG | 8945 |
rs574451588 | in-del | -/GGT | 0.00318978 | 0.0398085 | intron-variant | BTRC | GRCh38.p7 | 10:101376776 | TAGGTCATAGGGTAA[-/GGT]GGTGGTGGTGGTGGT | 8945 |
rs574460414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429836 | GTTGCTGTCAAAGCC[A/G]TAGGGATACAATACT | 8945 |
rs574486306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101364857 | CGGAGCGAGTGCACC[A/G]TTCCTGGAGGTACTG | 8945 |
rs574520092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101479597 | CAGGCATCATTTTAT[C/T]TAGAACAGATTGCAA | 8945 |
rs574535767 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556615 | ACATAGTATCGGAAA[A/G]AGAGCCATTTCTTAG | 8945 |
rs574541400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453377 | AATGATAGAATTATC[C/T]CAGTTACAGAGTCCT | 8945 |
rs574574175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101394788 | TGTCAGATTAGGGCA[A/G]GAATAGCAATTTGAC | 8945 |
rs574589894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101470637 | GCCTAGCCGGTTTTT[C/T]CTTTTAGAAGGGATA | 8945 |
rs574608069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453949 | CAGCCACAGACAAAT[C/T]GTAAATGGATGGGCA | 8945 |
rs574670329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101413164 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTAGAGTGC | 8945 |
rs574745677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405632 | AAAAGTCTTCTCCAA[C/T]TACCTGCTAGTATTT | 8945 |
rs574791353 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101408305 | TTTCTTCTTTTTTTT[A/G/T]AAATTTATTTTCTTT | 8945 |
rs574805151 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404876 | GGTGGCGGGTGCCTG[C/T]AGTCCCAGCTACTCA | 8945 |
rs574809949 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BTRC | GRCh38.p7 | 10:101445866 | TTATTTGCTTAATGA[C/T]GGGGAGGGTGTTAAA | 8945 |
rs574810181 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101436619 | GACCCTGTTTCAATT[A/T]AAAAAAATAGATAGA | 8945 |
rs574828340 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101441620 | GTGGTGGCTCATGCC[-/TA]TATAATCCCAGCACT | 8945 |
rs574841398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548962 | GGAGACTGAGGCAGG[A/G]GAATCGCTTGAACCC | 8945 |
rs574842676 | in-del | -/TAATT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101492180 | CAAACATCACTTCTC[-/TAATT]TAATCCACATTTTCT | 8945 |
rs574843006 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101524095 | CAATTATACCTTTTT[A/C]AAATTTTTGTTTTTC | 8945 |
rs574905925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101506511 | TTGGGGGTGGGGAGG[A/G]CAGGCATTGATGAGC | 8945 |
rs574911610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101462401 | TAAAAAAACAGCAGC[C/T]GGGCAAGGTGGCTAA | 8945 |
rs574945020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101498014 | ACAGAGCGAGACTCC[A/G]TCTCTTAATTAATTA | 8945 |
rs574945652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522525 | TCCCAGATTCAAGCA[A/G]TTCTCCTGCCTCAGC | 8945 |
rs574987396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101381621 | TTATTTTTGAGAAAT[A/G]TAATTTTGAAGAGAG | 8945 |
rs575001336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101358224 | CTCCTGCCTCGGCGT[C/G]TCAAGTGGCTACAGG | 8945 |
rs575015367 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101443076 | TTTAGTAGAGACGGG[G/T]TTTCACCATGTTAGC | 8945 |
rs575031026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439302 | GAACCACAAGGTACA[C/T]GAGCAAAGCACCCTG | 8945 |
rs575032567 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497351 | AGCTGTGTGATCCAC[A/G]CCTTGTGTACTACAG | 8945 |
rs575038244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357396 | CAGTGAGCTGAGATC[A/G]TGCCATTACACTCCA | 8945 |
rs575040897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101455362 | ATTCTCTAGCTTTGT[A/G]CTGAACCTCTGAAAT | 8945 |
rs575044203 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101518866 | AAATAATCCTATTAG[-/TT]TTTTGTTAATTGCTG | 8945 |
rs575049076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396606 | TTTTTGATCTACTTA[A/G]GACAGGTATTAATGG | 8945 |
rs575070980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534965 | GGGGAATTCATATGA[A/C]AATTTGATCAAGGGC | 8945 |
rs575075366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101416890 | GAAATTTAGTCTGAT[A/G]ATAATTACTACATTA | 8945 |
rs575078124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101522979 | GGGAGGCCGAAGTGG[A/G]TGGATCACGAGGTCA | 8945 |
rs575088333 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436366 | ATATAAGTAAGGGGC[C/T]GGGCACGGTGATGCA | 8945 |
rs575103332 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485765 | AGGGAGCTAATAGGC[C/T]CGAGCTTGTCTTTGT | 8945 |
rs575108220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515702 | ACTTTTAGTAGAGAC[A/G]AGGTTTCACCTTGTT | 8945 |
rs575125936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101459837 | AGTATGGGCTAGTCA[A/G]TACTCAGGCTGTTAA | 8945 |
rs575130389 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516976 | GTTTGGGAGGTTTTC[A/T]TTATTGGGATTAGAA | 8945 |
rs575132800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101356241 | CCTGACCTCGTGATC[C/T]GCCCACCTTGGCCTC | 8945 |
rs575151590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101409346 | ACTTTTTGTGTATGA[A/C]TTCTTTCACTTACCA | 8945 |
rs575156168 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101463235 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT | 8945 |
rs575160795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401724 | ACACGTGTAATCCTG[C/G]CACTTTCTGAGGCTG | 8945 |
rs575185460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101410151 | ACAGGAGTTTACTGA[C/T]AAAGCTTCTTCTAGT | 8945 |
rs575218441 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101407924 | AGACAGGGTTTTACC[A/G]TGTTGGCCAGGATGG | 8945 |
rs575300623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551863 | TCTCTTGATGAGTAA[C/T]GTGAGGGGCAGCACT | 8945 |
rs575327368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101493292 | TCAAATTTGACAGCC[G/T]TTTTGCACCATTACA | 8945 |
rs575333715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101510281 | TAGGAGGCAGAGGTG[G/T]GTGGATCACGAGGTC | 8945 |
rs575374327 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101418242 | GTGTGGTGGCGGGTG[-/C]CTGTAGTCCCAGCTA | 8945 |
rs575405884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526280 | ATTTTTGGGGAGCCA[A/G]TGAGACCACTTCTCA | 8945 |
rs575421085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101385388 | AAAAAAAAAAAAGAA[A/G]AGAAAAAAAGTGAAA | 8945 |
rs575439807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101502707 | TTACCACTGTACTCA[C/T]AAAAAGCAATACCCA | 8945 |
rs575446464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101526940 | AGTCTAAGAGACTTC[A/G]CTAATTTTTTTGTTG | 8945 |
rs575452034 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101455376 | TGCTGAACCTCTGAA[A/G]TATAAGATGAAACAG | 8945 |
rs575454366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101398733 | ATGTTCCTGTGTTGT[C/G]GTTGAAAACTGTGTT | 8945 |
rs575467238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101467177 | TTTCTTTTTTCAAGA[A/G]AGCTCCTTTTCTTCC | 8945 |
rs575481583 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101383272 | TTTTGCCCATGCTGA[A/G]TTTGCCATTCTTTAG | 8945 |
rs575487312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101401906 | GCAGGGCAAAAAAAG[A/G]AGGAAAAAAGAAAAA | 8945 |
rs575492560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101518207 | GTGAGCCACCGCGCC[C/T]GGCCGAAGTAGTGTC | 8945 |
rs575529331 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432697 | CACTGAAAACAATTA[C/T]ACTCACAGTTTATTA | 8945 |
rs575603413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101419727 | CGGTGGGAAACATCG[A/G]GGGGCATGTTAGAGT | 8945 |
rs575615548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101472576 | CCCAGCACTTTGGGA[A/G]GCCAAGGTTGGGTGG | 8945 |
rs575616318 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428050 | TGCCTTCTCCTTCCA[A/G]TGTGAGAATCTCTGC | 8945 |
rs575627965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101370374 | TGGCCTCGGCCTCCC[A/G]AAGTGCTGGTATTAC | 8945 |
rs575637001 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354119 | CCGGGCGCTGCGTTG[A/G]CTGCGGCCTGGCACC | 8945 |
rs575643233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101509599 | TCTCTGTTGTTTAGG[C/G]TGAAGTGCAGTGGCA | 8945 |
rs575647559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101520487 | TTCAGTAAATACTTA[C/T]TGAATGAATCAATTA | 8945 |
rs575654326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101359063 | TTGAGGTTAACTTCG[A/G]AAGGCACTAACATGA | 8945 |
rs575681859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537774 | CAGAGTGTGGTGACA[C/T]GTTCCAGCTTGGTCA | 8945 |
rs575682283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101512545 | CAGTCAGTCCACTAT[A/G]TATTTCCCAACCTAT | 8945 |
rs575683902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101528340 | GTTTTGCTTGGGATT[C/G]GCACTAAATGGCAAG | 8945 |
rs575705715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101473132 | ACAGTGACTAAGACC[A/G]ATCTTTTTTTTTTCT | 8945 |
rs575714929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552335 | CGCGGGCACACAACA[C/G]CATGACCAGCTAATT | 8945 |
rs575739181 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101402205 | ATGTGAGGAGGTTAT[-/G]TTTTTTTAAAGCATA | 8945 |
rs575750303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411425 | TTTTCTTTTGAGACA[C/T]CAGATATGCATGTGT | 8945 |
rs575752607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434587 | AATAACTGATAAATT[A/G]GACTTCATCACTGTT | 8945 |
rs575762585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101412099 | TGTGTAGTTTCTAGT[C/T]GCTGAGCTTATAGTT | 8945 |
rs575765736 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101359846 | CTCAGGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 8945 |
rs575790876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101447616 | TCTGTAGTGGTATTT[C/T]CCATTCCATAACGCA | 8945 |
rs575794513 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101527595 | TCATCTCTACAAAAA[A/C]ATCAAAAAATTAGCT | 8945 |
rs575795633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101544673 | ACAACCTCCTGAGTA[A/G]CTGAGATTATTACAG | 8945 |
rs575812813 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101484168 | TGTCACTGTTTTTTT[A/T]TTTGAGACTAATAAT | 8945 |
rs575844672 | snp | A/C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101467582 | TCTTGTAAATACTTT[A/C/T]GTTTGGGGTTTGCAT | 8945 |
rs575858415 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557156 | TGTTCTCTAGACTCT[C/T]AAGTACTGACTGCTT | 8945 |
rs575878527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101386494 | AAGACTTTTTTGTGA[C/T]AATTTTAGATCAGCA | 8945 |
rs575880402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101377081 | CTTATACTCTTCCTC[C/T]ACCTCTAACCCCCTC | 8945 |
rs575952848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101367076 | TATAAATATATATAT[A/G]TATATTTTTTTCGAG | 8945 |
rs575970294 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101367758 | TTCGTAAGATGATTC[A/G]TTCAGGTTGTTGTGG | 8945 |
rs575977018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101481043 | CTTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGAAA | 8945 |
rs576002195 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504847 | TTTTGCTTGCTCTGA[G/T]CAATTTGATATTATG | 8945 |
rs576027147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101532874 | TTATTTTGGGGGATC[A/G]GACACGTAATAGGAC | 8945 |
rs576057955 | in-del | -/ATAGATAGATAGATAGATAG | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101436626 | TTTCAATTAAAAAAA[-/ATAGATAGATAGATAGATAG]ATAGATAGATAGATA | 8945 |
rs576058281 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101541364 | TCCTGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 8945 |
rs576064211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101524141 | AGTTGCTGTTTAAAA[A/C]AAAAGAAGTACCTAT | 8945 |
rs576076819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101423381 | AGATGCAGCTTGTTA[G/T]TTTGTTATACATATA | 8945 |
rs576098923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101464841 | ATCTGGTTTTTTGCT[C/G]GAACCAGATTACTGT | 8945 |
rs576114858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534190 | GGCTTAGAATTAGAG[G/T]CATGGTTATCTTGGC | 8945 |
rs576116112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101438281 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 8945 |
rs576149968 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556494 | GTCTGTAGCAGAGCA[C/G]TCCAACCCAGATTAG | 8945 |
rs576173690 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482696 | TGCCGCATCCGGCCA[A/G]CTGTTTCTATTGGCC | 8945 |
rs576202068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101430254 | GTCAGCTGCAACTGG[A/G]ATATTGCGTTCAGCC | 8945 |
rs576202585 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101497905 | CGTGCCTGTAGTCCA[A/G]GCTACTCAGGAGGCT | 8945 |
rs576220133 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352747 | TTTTAGACAGAGTCT[C/T]GTTCTGTTGCCCAGC | 8945 |
rs576231845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101507341 | TCAGAGTTTCTCCTA[C/T]TATATTTATCTTACA | 8945 |
rs576232647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101439114 | TGACAAGTCAGAAAT[C/G]CATTAGATCATTCTC | 8945 |
rs576244260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101373345 | GTATGTAATAGTCTA[C/T]GCAAGAGACTGGGCT | 8945 |
rs576262526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101376215 | CCTGTAGTCTAGCTA[C/T]TTGGGTGGCTGAGGC | 8945 |
rs576320832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508607 | CTTTGATCACTGAGA[A/G]TTATAAAGTTTAAGA | 8945 |
rs576323369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101391035 | TTTTATAAGAATTTT[G/T]CCTAAAGAACTTTTC | 8945 |
rs576330211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101548795 | CACAGTAGCTAAGGC[A/C]TGTAATCCCAACACT | 8945 |
rs576334891 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101374124 | CCAGTTCTAGATCCC[A/G]GAGGAATCGCCACAC | 8945 |
rs576382624 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BTRC | GRCh38.p7 | 10:101542576 | TGACAGCTTTTGCTT[C/T]GTGGTTTTTGTTTGA | 8945 |
rs576384573 | snp | G/T | 3.36168e-05 | 0.00409967 | intron-variant | BTRC | GRCh38.p7 | 10:101550908 | TATCGAAATCGATTA[G/T]GTACATAACACTGTG | 8945 |
rs576391296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101381550 | GTAGAATTAGCATGC[A/G]CCTTAGAGTAGGTAT | 8945 |
rs576393344 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101476479 | CTTTTTCTTTCTTTC[-/T]TTTTTTTAAAGAGAT | 8945 |
rs576401891 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101491143 | GCCTTATTAACATAG[C/T]ATACAGATCTTTCAA | 8945 |
rs576412996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101492055 | AATTTTTCACACAGA[C/T]TCATAAAGTATGTAA | 8945 |
rs576427709 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469714 | CACCCTAATTAAACT[A/G]TAGAATATTTTCATA | 8945 |
rs576428278 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383062 | TCCCTGGAGATTTTT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs576429847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101432845 | TACTGCCTCCCAGCC[A/G]CAGTGTGTGACAATA | 8945 |
rs576443621 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101433635 | AGTGAGAAAAGACTG[G/T]GGAAGCTTGATCACT | 8945 |
rs576466789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101375609 | GAATACTAGAAACAG[A/G]TAGCAAAGCGTTGCT | 8945 |
rs576488999 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101440224 | TGTTTTAAATTACAT[A/C]TTTTTTTTCAAGCTA | 8945 |
rs576544654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101537951 | CTTATATAAACTCCA[C/T]TGCTCTTACATGGAC | 8945 |
rs576544667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101546760 | AAGCTAGTTCTTTGA[A/G]AGGATCAATAAAATG | 8945 |
rs576562420 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101517145 | ACAAGGTTCTTAGTA[A/G]TCATTTTTAGTCTGT | 8945 |
rs576579138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101457542 | AGTAACTGAAATTGC[A/G]TGAGTGAAACTGTGG | 8945 |
rs576596932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101458273 | AGATTCAAAGGTTAC[A/G]TACGATATAATTCCA | 8945 |
rs576599310 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557499 | CTTACGCCTACTGTT[C/G]CATGTTGAGTTAAAT | 8945 |
rs576609782 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | BTRC | GRCh38.p7 | 10:101398877 | TTCATCAATAACCTC[C/T]TCACTGTATACATTG | 8945 |
rs576631479 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354551 | TGAAAAGCGGAGGAA[A/G]CTCTCTGGAGAAACG | 8945 |
rs576632476 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BTRC | GRCh38.p7 | 10:101520402 | TATATGTTAGTGATG[C/T]TAGAGACTGTCATTT | 8945 |
rs576650768 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BTRC | GRCh38.p7 | 10:101435438 | GAACTTACTTCATAT[A/G]AATGCCATCATATAG | 8945 |
rs576655827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474295 | TGGTTTTGTATTTGT[C/T]AAGGTCAGGTGTATT | 8945 |
rs576701422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101499245 | TGACACTATGCAGTA[C/T]TACCTTTTTTTTGAG | 8945 |
rs576705076 | in-del | -/TTCT | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101390978 | AGTAAATACAAATGG[-/TTCT]TTATCAAATTTAGAA | 8945 |
rs576720383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394118 | TCTATTTAGAAGATA[C/T]TATGGAGCTAGAGGT | 8945 |
rs576726941 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101429443 | TATTTTTGTTTGTTT[C/G]TTTAGAAGGTTTTAA | 8945 |
rs576730141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101435452 | TAAATGCCATCATAT[A/G]GTGTACATTCTTTGT | 8945 |
rs576738371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101394686 | AAAATTCTTAGCAGT[C/T]GGGGCAGGGTATAAC | 8945 |
rs576750722 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553726 | ACAAGAATGTATACA[C/T]TGGAAGATTTGGGCC | 8945 |
rs576777467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495126 | CCTAATACTGACCTA[C/G]TTTGCTCTTAGACAA | 8945 |
rs576805183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101436428 | GGCTGGCGGATCACA[C/T]GAGCCCAGGAGTTCG | 8945 |
rs576825168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101454219 | GTAATGTGTTAGTGG[A/G]TAGAGGGAGCTACAA | 8945 |
rs576825810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101495735 | TGTTCATCCTTATTG[A/C]CCTTTCTGTGAATAC | 8945 |
rs576828254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101440573 | CAAAAATACAAAAAA[G/T]TAGCCAGTCATGGTG | 8945 |
rs576828360 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101416577 | ATTGTTGTTGTTGTT[G/T]TTTACCAGGGTACCT | 8945 |
rs576832530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449428 | AGAGGTCGAGTTACA[A/G]AAATAACCAGATGTC | 8945 |
rs576845106 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101508359 | CTTTCCCTCTACTGA[A/C]AAATCTGCCCCTTCC | 8945 |
rs576846389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101378875 | AGTATTCAGTAATAT[A/T]TTGAAATGAGAAATA | 8945 |
rs576850207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101437408 | TTATCCATCCATGTG[C/T]GCCTGTGCGTGCACA | 8945 |
rs576860868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101445091 | TTCATTTGAAGATAC[A/G]ACTATATATTTTCAG | 8945 |
rs576884726 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433628 | AGAATAGAGTGAGAA[A/G]AGACTGGGGAAGCTT | 8945 |
rs576885849 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101355330 | TTAGGTTGAAGCACA[-/GT]GTGAGCAAAGATTGG | 8945 |
rs576916657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101379386 | TCTTGTGGAAAAATA[A/T]AATCTTTTGAAAGCA | 8945 |
rs576923560 | in-del | -/A/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101373939 | AAACAAACAAGACAG[-/A/AA]AAAAAAAAAAAAAAG | 8945 |
rs576959737 | snp | A/G | 0.000159771 | 0.00893645 | intron-variant | BTRC | GRCh38.p7 | 10:101414637 | ATGACAGGTCCATAG[A/G]TGTTAATTGCTCCCA | 8945 |
rs576963179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101460669 | GAATGACACAGTACG[G/T]TTTTTATCTCTCAGT | 8945 |
rs576966295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101485742 | TTTATTCATATTTCT[A/G]TCTAGCCAGGGAGCT | 8945 |
rs576974226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101538908 | AAAAAAAAATTAGCC[A/G]AGCATGGTGGCAGGT | 8945 |
rs576991516 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438404 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTGC | 8945 |
rs577027519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101421004 | TTTCTTACATACTAG[A/T]TAGAGGTTTACTATC | 8945 |
rs577032137 | in-del | -/CCCCCCCA | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101446103 | CATTTTGTTCTCTTC[-/CCCCCCCA]CCCCCCCAACCCCCT | 8945 |
rs577065681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101403526 | TGCTGTTGAGACCAT[C/T]CAGTGAGTTTAAAAA | 8945 |
rs577067747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101552675 | TTGAAGATAGCAAGA[A/G]CACTTCTAGTGCTCA | 8945 |
rs577076532 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377092 | CCTCCACCTCTAACC[C/T]CCTCTTCCTCACTTC | 8945 |
rs577080732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101413001 | AATGAAGTTATAGAA[A/G]AAATAGTTGACCATA | 8945 |
rs577088304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101444272 | ATATTTGTTACAATG[C/T]CTCCTACTGGTTGAT | 8945 |
rs577090668 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101524548 | TTCAAAAAGTGCCTG[C/T]AGTCCATTAATGTAA | 8945 |
rs577097428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101494324 | CAGAGTACAAGAGAG[A/G]AAGTCATACTGATTT | 8945 |
rs577108152 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | BTRC | GRCh38.p7 | 10:101378418 | CTTCTTTTTAATGAC[-/TG]TGAGTTTTACAGTTA | 8945 |
rs577132752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101522380 | AACAAAAAAAAACAA[A/C]AAAAAAAAAACTCTA | 8945 |
rs577143379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101452390 | GCTATAACCAACCTA[C/T]CCATCTGCCAACCAG | 8945 |
rs577152835 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101541793 | CACTTGTTCATGAGG[-/TA]TATAATTCTTTTTAT | 8945 |
rs577202534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101395920 | TGTTTTGTTTGTAAG[C/T]GACAAATATGTATAT | 8945 |
rs577208450 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101458365 | GGGAGAGGGTTGACT[A/G]TTAAGGAGAATTTCA | 8945 |
rs577224269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101453181 | GGAAAAAGTATTAAT[C/G]CAATTACTAATTTAC | 8945 |
rs577246028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101449615 | GGAAAGCAGTTTTTT[A/G]AAAGATTCCTATAGA | 8945 |
rs577262761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101396502 | TGGAGTTCAGCTAGT[A/T]TTAAGCCCACTACTC | 8945 |
rs577277500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101513867 | CTTGTTTTCCAAAGT[A/G]GTTGTACCATTAAAC | 8945 |
rs577294751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101497156 | CCTAGCACCATTTAT[G/T]GAAATGTGTAGTTCC | 8945 |
rs577304670 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101502392 | GAAAGATTGAAAATG[-/A]AAAAAAAAAAATCAA | 8945 |
rs577314722 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514819 | ATTTCTGGACTCACT[A/T]TTCCTTTCCATTGAT | 8945 |
rs577323821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101372146 | ACTGTCTTAATTTCT[A/G]TATTTTTATATAATA | 8945 |
rs577336145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101429204 | TTTTAGTTATTATTA[G/T]ACTGTAATAGCACTC | 8945 |
rs577381885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101432762 | AAGAGACACATAGGG[C/T]AGAATCTCGGAAGGA | 8945 |
rs577404593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101530509 | GGGAAAAAAAAAAAA[A/G]CCTATAGGGCATGTG | 8945 |
rs577456518 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101469086 | TATAAAAACGTATTA[A/C]AGTACTCCAACGCAA | 8945 |
rs577471088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363990 | TTGTGGGTTTGCTGG[A/G]TAGTGGATGATCTAA | 8945 |
rs577479652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101462172 | ATATTAAGAGTACTC[A/G]GACGTTGGCCTGGCC | 8945 |
rs577480994 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439685 | TGTTAAAGAGAAGTG[A/G]TGCTGATGGAGCCAA | 8945 |
rs577487475 | snp | C/T | 0 | 0 | intron-variant | BTRC | GRCh38.p7 | 10:101404452 | ACCAAGTAATTTTTG[C/T]GTTATATCCTTGGCT | 8945 |
rs577533940 | snp | C/T | 0.000290899 | 0.0120567 | intron-variant | BTRC | GRCh38.p7 | 10:101526221 | CTTTAACTTTTCTTA[C/T]TCTTATACGGCTTCA | 8945 |
rs577566310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101508685 | TTTGGGAGGCCGAGG[A/C]GGGCAGATCACGAGG | 8945 |
rs577574944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101369919 | GTTGCTGCTGTTCCC[C/T]ACACCCACTATATAG | 8945 |
rs577585897 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101354046 | CCGATTCTCCTTGGC[C/T]CCTCAGCCTGCGCCT | 8945 |
rs577634740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101362488 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCTATTC | 8945 |
rs577644318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101357107 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 8945 |
rs577655784 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | BTRC | GRCh38.p7 | 10:101509544 | CAGGCGTGAGCCACC[A/G]CGCCCAGCCTTTTTT | 8945 |
rs577664658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BTRC | GRCh38.p7 | 10:101378085 | GTAGCATAGATCAAT[A/G]GTATGATTTTAATAA | 8945 |
rs577666714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101361579 | GCAATGGAGGGGGGA[A/G]GAAATCTCTATGGGA | 8945 |
rs577719332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BTRC | GRCh38.p7 | 10:101419260 | AGGCGATCCACCCAC[A/G]TCGGCCTCCCAAAGT | 8945 |
rs577728127 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | BTRC | GRCh38.p7 | 10:101355616 | CAGAAGTTATTGTGA[C/G]TTGTCACTCCAAATC | 8945 |
rs577747303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101363003 | AGAGACTTTTGAGTA[C/T]CTGTGGATTTTGGTA | 8945 |
rs577766419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101451489 | ACTGAATGTGTCATG[C/T]GCTTTGACATAACAT | 8945 |
rs577807192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101415897 | TTTAGATACACAAAT[A/C]CTTTCCACTATATTG | 8945 |
rs577810105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101534071 | AATATATAATCACAC[A/G]AAATTCTCAAGCTAT | 8945 |
rs577828540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101416694 | TCTTACTCTCTGCGT[A/G]TAAAATTTAGGAGTC | 8945 |
rs577830829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101474260 | AATTACTGGCTGATC[A/G]CTATGACCTTGTGGA | 8945 |
rs577839399 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101536118 | AGAGCTGTCCTGGAC[A/C]GTGGTGAAAGAAGTG | 8945 |
rs577849050 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482120 | CACCTCCTGGGTTCA[A/G]GCCATTATCCTGCCT | 8945 |
rs577868768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BTRC | GRCh38.p7 | 10:101483432 | ACCCTGTCTATACTA[A/G]AAGTATAAAAATTAG | 8945 |
rs577886771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101417273 | ATACATTTAGTAGTC[A/G]TACCTCTTTAGTCTC | 8945 |
rs577900346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101482556 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 8945 |
rs577921936 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101536198 | TAATCTGTATCTCTT[A/T]CAGTTTGGTGACTTC | 8945 |
rs577931325 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BTRC | GRCh38.p7 | 10:101360126 | GTGGTGCAACCTTGG[C/T]TCACTGCAGCCCCTA | 8945 |
rs577964379 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527675 | GGGAGGATGGCTTGA[A/G]TCTGGGAAGTTGAGG | 8945 |
rs577966111 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547153 | AGTTTCATTTACAAC[A/G]GGTTCATCAGGATGT | 8945 |
rs577984243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101525227 | ATTGGGAAGCCCTTC[C/T]GGTTTACACTCCCCA | 8945 |
rs578012922 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511457 | CTCTGTTGCCCAGGC[A/G]TTCAAGCAGTTCTCG | 8945 |
rs578014476 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | BTRC | GRCh38.p7 | 10:101422322 | TGATGGGGTTGTTTG[-/T]TTTTTTTCTTGTAAA | 8945 |
rs578023047 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | BTRC | GRCh38.p7 | 10:101460803 | AAATTTTCAGATAAA[-/CT]CTCATGTTAAAAATA | 8945 |
rs578042325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101468746 | TAAGCAGCTTTTTGC[A/G]AGGTTAAAACAATGC | 8945 |
rs578049932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101411202 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTCGAAC | 8945 |
rs578121937 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101501358 | TGAGCTTCAGATAAT[A/C]CCATCCACTCACTCA | 8945 |
rs578134389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101361138 | TTGAGACGGAGTCTC[A/G]CTCTATTGCCCAAGC | 8945 |
rs578140730 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BTRC | GRCh38.p7 | 10:101443007 | CTGCCTCAGCCTCTC[C/G]AGTAGCTGGGACTAC | 8945 |
rs578154275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434207 | TCTGACCTGGCATAG[A/G]TATATAGTTTGAAAG | 8945 |
rs578172892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101434511 | GCAAAAATAATCATT[A/G]TGACTTTGGGTTAGG | 8945 |
rs578207121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101551299 | CAGTCTGATGTCTAA[C/T]GTGTGAATGGAAACA | 8945 |
rs578213433 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362993 | AGGCACTATAAGAGA[C/G]TTTTGAGTATCTGTG | 8945 |
rs578231412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BTRC | GRCh38.p7 | 10:101542884 | TTTTTTTGTTGTTGT[C/T]GTTGTTTTTGAGACG | 8945 |
rs745311049 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352535 | CCACCCAAGTAGTGA[C/T]GAATCCCTATTTCTT | 8945 |
rs745323285 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101368163 | AAATAAGTGAGTTCT[C/T]GCTCCATTAGTTCCT | 8945 |
rs745323435 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514043 | TGTTGAACATCTTTT[C/T]ATATGCTTATTGGCA | 8945 |
rs745373191 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101431776 | ATTTTTAATGATACT[A/G]TTTAGTGATCATAAA | 8945 |
rs745397680 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423843 | AATAAATGGCTTCCC[A/G]GAACAGTTTGAAATG | 8945 |
rs745403495 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459739 | CCTTTGTGTTTTCAT[A/T]CTTTAGACATTTTCA | 8945 |
rs745421463 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532493 | GACCACATTCATAGC[A/G]CAGTCTAAAGCATAA | 8945 |
rs745423152 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534754 | TAATGGCATGATGGT[A/G]ACCTGCTCCAAAGAT | 8945 |
rs745438006 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383704 | TTTCTTTAATAGATA[C/T]GAGAATAATATGGAT | 8945 |
rs745460851 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476829 | ACTGTTGGTTTTGAG[C/T]GTCTTAAGATTTTTC | 8945 |
rs745463969 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101499668 | CCTAACCCCCATTCT[C/T]ACTGCTGCTCTCCTA | 8945 |
rs745476004 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101403061 | TCATTTAGCTTTTGT[A/G]AAGTCAATCCAGTTT | 8945 |
rs745514931 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101393195 | GTGGTGTGCCCAGGG[A/G]GTCATGGCAGCTCTG | 8945 |
rs745520934 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354266 | GGAACGGTGGAGGCG[C/T]TGGCGTTGGCGGCGT | 8945 |
rs745539316 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498789 | GAAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 8945 |
rs745550951 | snp | G/T | 0.000108666 | 0.0073703 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354159 | GCCCCGGCGGAGAGC[G/T]GACCCAGTGGCCTCG | 8945 |
rs745562887 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101434124 | AGAAAAGACAGCTGG[A/C]TTCTCATGTCTGCTT | 8945 |
rs745563658 | snp | G/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353472 | ACCGAGTTCTATTCG[G/T]CCCTGACTTGCTGTG | 8945 |
rs745566179 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460639 | GGTGTCAGCCACAGA[A/G]GTGAAAGGGCCTCAG | 8945 |
rs745571697 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515247 | AGGTGTGAGCCACCA[C/T]ACCTAACCGTTTTTT | 8945 |
rs745579743 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377043 | AGGATAAGAACAATT[G/T]TATCACTCCCCCGCA | 8945 |
rs745606399 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101416470 | ATCCCTTTGGTTCAG[C/T]TGAGGCATCTCTGTT | 8945 |
rs745608601 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538559 | ATCCAAAAATGCTTT[A/G]GAGACTATATATGGA | 8945 |
rs745628596 | in-del | -/ACACACACACAC | | | intron-variant | BTRC | GRCh38.p7 | 10:101455987 | CTCTACTAAAAACAC[-/ACACACACACAC]ACACACACACACACA | 8945 |
rs745650332 | snp | C/G | 9.885e-05 | 0.0070296 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536629 | GATTTGATAACAAGA[C/G]GATAGTCAGTGGGGC | 8945 |
rs745673840 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537138 | TTCATTTATGAGTTT[A/G]GTCATCTTTATTTTC | 8945 |
rs745681559 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555061 | CTTCCCAGCTACCCA[A/G]ATGCTACAGAGAAAT | 8945 |
rs745696423 | snp | A/G | 3.46188e-05 | 0.00416032 | intron-variant | BTRC | GRCh38.p7 | 10:101526230 | TTCTTACTCTTATAC[A/G]GCTTCAGGACCTGGC | 8945 |
rs745735210 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101378522 | GCTCCCAATTATAAT[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs745736103 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556246 | GTCTAAAGCTACAGA[-/G]GAAAAAAAAATGCAC | 8945 |
rs745738721 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101471653 | CACTTGTGTATAATC[C/T]TGGTGGTGTTTCTTC | 8945 |
rs745753346 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421696 | TTTCATTGTTCAATT[C/T]CCACCAAGAGTGAGA | 8945 |
rs745754084 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454951 | GCCTAGAACTTCATA[C/T]TTGATTTCATAGAAA | 8945 |
rs745797916 | in-del | -/CT | 1.64747e-05 | 0.00287003 | frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538351 | GCTCCTGCAGGGACA[-/CT]CTGTCTACGGACCCT | 8945 |
rs745817943 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361504 | AAAGTTTAACAACTT[A/T]GTCAATAAAAATAAA | 8945 |
rs745843267 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101449350 | AAGAATTTTGTCATA[C/T]GTCCTAAGGGTTCTA | 8945 |
rs745860042 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433125 | CCAAGAGGAAAGGCC[A/G]TTCCTTTCTTTGGTG | 8945 |
rs745867365 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487304 | CTTCATTGCTATATA[A/G]TTTGTGTCAAAACCA | 8945 |
rs745871618 | in-del | -/TTTTTGTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101363456 | TCGTTTTTGTTTTTG[-/TTTTTGTTTTTT]CTTTTTTTTGAGATG | 8945 |
rs745874643 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101523994 | ACATTTTAAGGCTTT[C/T]AATACATGGTGCCAA | 8945 |
rs745877690 | snp | A/G | 1.65592e-05 | 0.00287738 | intron-variant | BTRC | GRCh38.p7 | 10:101461942 | AAGGATAAGATTGAA[A/G]ATAATGAGAACTGAA | 8945 |
rs745902079 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403785 | TTTTCTGTAGAGACA[G/T]GGTCTTACCCTGTTT | 8945 |
rs745904192 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101387012 | TTACAATGGCCCCCA[A/G]CATCATTTATTGGAA | 8945 |
rs745921966 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510881 | CATTTCCTAATCTGC[C/G]TAATCTAATCCTAGC | 8945 |
rs745922101 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493999 | TTCTAGTTCATGATG[C/T]ACAGCTCCCACCAGA | 8945 |
rs745933497 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant | BTRC | GRCh38.p7 | 10:101533105 | TTTTTGAACTCTGAA[A/G]TATCAGCTCTGCTCT | 8945 |
rs745954435 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101402720 | TTAAGTGAACTTCTC[A/G]AAGTCATACAATTGG | 8945 |
rs745962327 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101390818 | AGGGTGAATGTACTG[C/T]CCAGCACTCTCTTCT | 8945 |
rs745995271 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526601 | CCTGGCCAACGTGGC[A/G]AAACCCCAACTCTAC | 8945 |
rs746001139 | snp | A/G | 0.0235261 | 0.105875 | intron-variant | BTRC | GRCh38.p7 | 10:101462107 | TACCAACAGCAAAAC[A/G]AAAGACAGGAGGAAA | 8945 |
rs746031296 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554228 | TTCATCTTAAATCAC[-/T]TGGTAAGGCTCAGCC | 8945 |
rs746047947 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481690 | TGAGAAAGTAAGTTT[G/T]CTCATTGCTGCTCAT | 8945 |
rs746053325 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369326 | CTGGGCTCAAACATC[C/T]TCCCACCTGGGCCTC | 8945 |
rs746066817 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360641 | CTCCCAAAGTGCTGG[A/G]ATTATAGGCATTAGC | 8945 |
rs746088716 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101443369 | GCAAATAAATACACT[G/T]AGGACAACTCAACAT | 8945 |
rs746121807 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533002 | TCTCACAGGCCATAC[A/G]GGTTCAGTCCTCTGT | 8945 |
rs746124087 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464352 | ATACAGATGGACCAG[C/T]AGGTCACACATGGGA | 8945 |
rs746145943 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101479746 | ATTTGTATAAGATAA[C/T]GTACAATTGTTTTGA | 8945 |
rs746154458 | snp | C/T | 6.71558e-05 | 0.00579425 | intron-variant | BTRC | GRCh38.p7 | 10:101550902 | CCCAGGTATCGAAAT[C/T]GATTATGTACATAAC | 8945 |
rs746159739 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495445 | AAAAATAAAAATCAC[C/T]GTATTGCATTTAACC | 8945 |
rs746173723 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518613 | TTAGTTACCACCACC[A/G]GAATGACCAGGATGA | 8945 |
rs746182846 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412016 | TTTCTAAGGCTCCTA[A/G]TGAATGTCATAAGTA | 8945 |
rs746185273 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356523 | AGATGACCATATAGT[A/G]GTTGCAGCTTTTAGA | 8945 |
rs746204634 | snp | C/T | 1.65548e-05 | 0.002877 | intron-variant | BTRC | GRCh38.p7 | 10:101550696 | TTGTTTCTACTTCTT[C/T]AGGAGCATTCCGGAA | 8945 |
rs746204869 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514065 | TTATTGGCATCTGTG[G/T]ATCTTTTTTTGTGAA | 8945 |
rs746223485 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556908 | CAGTGCAGTTAAGTC[A/G]TATTTTAAAGTGTTA | 8945 |
rs746235706 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410821 | AATATTTCACTTCAC[A/G]TATACTGTATTTTCA | 8945 |
rs746259842 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543894 | TTGCTTTAAACAATC[A/G]ACCATCTTTTAAGAT | 8945 |
rs746265219 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516895 | TAGCACCCAACTCAT[A/G]TCCATTTCCACCTTT | 8945 |
rs746265335 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533392 | AATGATATGAATGCA[A/G]TGAAGCCTTCCTTTC | 8945 |
rs746266804 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445259 | TATTTGTAGGAGTAT[C/G]AGCTCTCAAATATGT | 8945 |
rs746307629 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101370689 | ATCCTCCCACCTCAA[C/T]TTCCCCGTAGCTGGG | 8945 |
rs746310803 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488893 | AGGTGATCTTTTCTC[A/T]TAGGACTTTTTTTCA | 8945 |
rs746324883 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486019 | ACAGTGCGATCTGCG[A/G]GGCTGTAATTGCATT | 8945 |
rs746325387 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397736 | TCATACCCTGTTACT[G/T]TATCATTTTAGTCTT | 8945 |
rs746359055 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101520399 | AGTATATGTTAGTGA[-/TG]TGTTAGAGACTGTCA | 8945 |
rs746365718 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434955 | AAGATTATTATTATG[A/T]CTTATGTAGCAAAAA | 8945 |
rs746365975 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502782 | TTGAGCTGCTGTTAT[A/G]TAGATACTGAAAACT | 8945 |
rs746371780 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451490 | CTGAATGTGTCATGC[A/G]CTTTGACATAACATA | 8945 |
rs746388633 | snp | A/C | 1.66913e-05 | 0.00288883 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521869 | CATAACTGCTCTGCC[A/C]GGTATGTCTACAAGT | 8945 |
rs746388725 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101357857 | TAACTTTTAAAAACA[A/G]ATAAATGATATTGAA | 8945 |
rs746423400 | in-del | -/AAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101510665 | CCTGGCCGCAGGAGC[-/AAG]AACACTGTTGTATCC | 8945 |
rs746447318 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364245 | GATTGGATACTCCTA[C/G]AATCATAATGTAATA | 8945 |
rs746460151 | snp | C/T | 1.67214e-05 | 0.00289144 | intron-variant | BTRC | GRCh38.p7 | 10:101526205 | GAAGAGGATGGTGAG[C/T]CTTTAACTTTTCTTA | 8945 |
rs746461841 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527535 | AGGCAAGAGGATCGT[C/T]TGAGCCCAGGAGTTT | 8945 |
rs746483721 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420863 | TTAAATTTTATTTTT[G/T]AAAAACTCACTGGTA | 8945 |
rs746489393 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473609 | CCAAGTAGCTGGGAT[C/T]ACAGGCACTTGCCAC | 8945 |
rs746499840 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101490251 | CCTCACTCCCTGCCT[A/C]CCTCCCTTCCTTCCT | 8945 |
rs746518865 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456598 | CTTTCTTTTTTATTC[A/G]CCCAGTTTGGTTGTG | 8945 |
rs746533476 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436083 | AAATTCTATGGGGAT[A/G]TGTTTAGTTTGAGGA | 8945 |
rs746537300 | snp | A/C | 0.000112152 | 0.00748754 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354142 | CTGGCACCAAAGGGG[A/C]GGCCCCGGCGGAGAG | 8945 |
rs746570705 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380516 | TCCTCACTTCCCAGA[C/T]GGTGGGGCGGCTGGG | 8945 |
rs746584220 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360370 | AGAGATGGGATCTGC[-/T]TTTTTTTTTTTTTTT | 8945 |
rs746600113 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101399034 | CTTGGCTCACTGCAA[C/T]GTCCGCCTCCTGGGC | 8945 |
rs746605425 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396888 | GCTCACCGGAACCTC[C/T]GCCTCCCGGATTCAA | 8945 |
rs746611624 | snp | A/C | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101513873 | TTCCAAAGTAGTTGT[A/C]CCATTAAACGTGACT | 8945 |
rs746623046 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497792 | TTTGGGAGGCCAACG[C/T]GGGCATGTCACAAGG | 8945 |
rs746649064 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405525 | TCTTTACTGACACCA[A/G]TACCCACTTGTGGGT | 8945 |
rs746684260 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366111 | CCCTTTATGTATCCA[A/G/T]GGTTTTCATAGGAAA | 8945 |
rs746691613 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101532270 | TGTTTCCTAACACTG[A/C]CTCTTTCCCATTCCT | 8945 |
rs746695405 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352753 | ACAGAGTCTCGTTCT[A/G]TTGCCCAGCCTGGAG | 8945 |
rs746696236 | snp | G/T | 3.29484e-05 | 0.00405871 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536603 | CCATGAGGAATTGGT[G/T]CGTTGTATTCGATTT | 8945 |
rs746699506 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528655 | CTTGTTGCTGCTTCT[A/G]TTTTTACATGTTGAC | 8945 |
rs746716255 | in-del | -/AAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101491059 | GCAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAACTC | 8945 |
rs746723443 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512666 | CTCCTGGCCCAGGCT[A/G]CAGCTTCAGAGAAAT | 8945 |
rs746795359 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101552538 | TCCTTCTTAGGCTGC[C/T]TTCTCTATTCCCAAG | 8945 |
rs746797675 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445433 | AGCTTCTGTTTAAAT[C/T]AGTAGAAAATATGTT | 8945 |
rs746799908 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536111 | TCTGAGAAGAGCTGT[C/T]CTGGACAGTGGTGAA | 8945 |
rs746845716 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352387 | AACTGGGTCTGTCTT[A/G]TTCATTAATGAATCC | 8945 |
rs746861338 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392019 | GAGGCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8945 |
rs746892941 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485383 | ATCAGACTGGCTGTT[G/T]TTAAGCCTGAAGTCC | 8945 |
rs746904503 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468512 | TGCATCTATTGAACA[A/G]GATTCAGTAGCATCT | 8945 |
rs746922856 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369129 | TACTGTAAACAAGCA[C/T]CTTTTTAGGTTTGTT | 8945 |
rs746947796 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101431422 | AGTTCCAGGATGTGC[A/G]AGAAACTTATAGAGA | 8945 |
rs746972098 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551447 | CTTTTGACCTCTGAC[C/T]TCCACATGTCCTCCC | 8945 |
rs746988971 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101443617 | GAAAAGTTTTAATTT[A/C]TTCTATGTAATCTTC | 8945 |
rs746995431 | snp | A/G | 4.97055e-05 | 0.00498501 | intron-variant | BTRC | GRCh38.p7 | 10:101461933 | TTACTCCCAAAGGAT[A/G]AGATTGAAGATAATG | 8945 |
rs747012670 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366521 | GGAGAAATTAGTTTT[A/G]ATGAGAGATTTTTTA | 8945 |
rs747014929 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484124 | GTAGCCCTTTGTGGA[C/T]GTTCTGTATTTTAGT | 8945 |
rs747021469 | in-del | -/AAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101523207 | AGACTCCATCTCAGA[-/AAAT]AAATAAATAAATAAA | 8945 |
rs747059819 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101390355 | TTTTTTTTTTTTTTC[-/C]GAGACGGAGTCTCGC | 8945 |
rs747082773 | snp | A/C | 1.64766e-05 | 0.0028702 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550815 | AGCTGCCCAAGCTGA[A/C]CCCCCCCGTTCCCCT | 8945 |
rs747086811 | snp | A/G | 1.74787e-05 | 0.00295619 | intron-variant | BTRC | GRCh38.p7 | 10:101532461 | AGTTGTAGAAAGGTA[A/G]CAGAGGGAGCAAGAG | 8945 |
rs747096634 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416141 | GGCTTATTTCACTCA[A/G]CATAATGTCCTCAAG | 8945 |
rs747102153 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520538 | AATACGGAATATTTT[A/T]TGTTATGGAAAAAGG | 8945 |
rs747106103 | snp | C/T | 3.30153e-05 | 0.00406283 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430384 | CTGGGCTGCTCCAGC[C/T]TGGCGGACAGCATGC | 8945 |
rs747112756 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453367 | GCTTTGCTAAAATGA[C/T]AGAATTATCCCAGTT | 8945 |
rs747120648 | snp | A/G | | | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521708 | TCAGCAAGCTATGAA[A/G]AGGAAAAGGAACTGT | 8945 |
rs747135778 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553234 | TCAAACTACTGCCCA[A/G]TTTCCCTGGACTAGC | 8945 |
rs747139815 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532981 | CACATTGGAATGCAA[A/G]CGAATTCTCACAGGC | 8945 |
rs747156462 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359463 | CCCTGAGTCTCGCTC[C/T]GTTGCCCAGACTGGA | 8945 |
rs747168061 | in-del | -/TATATACACATATATATATATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101505121 | ATATATTTATATATA[-/TATATACACATATATATATATG]TATATGTGTATATAT | 8945 |
rs747179587 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385074 | ACAAACAGAACAAAA[C/T]AGAACAAAATTAGCG | 8945 |
rs747205679 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493892 | CCAGGGTTCTGAAGC[C/T]TTTGGATGCCACAAA | 8945 |
rs747242089 | snp | C/T | 1.66363e-05 | 0.00288407 | intron-variant | BTRC | GRCh38.p7 | 10:101550684 | TTCCTACCCTTTTTG[C/T]TTCTACTTCTTTAGG | 8945 |
rs747258755 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101508013 | ACCTATCACCCTGGA[A/G]GCTATAAAGTTGCAT | 8945 |
rs747261046 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101494083 | AAACACAGCTCTTGA[C/T]TGAGGCTATCAGCAG | 8945 |
rs747274550 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547401 | GGAGTAGTGCAATGG[C/T]GCAATCTCGGCTCAC | 8945 |
rs747307086 | snp | C/T | 1.67329e-05 | 0.00289243 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521675 | TCCAGTATGATTGTG[C/T]CCAAGCAACGGAAAC | 8945 |
rs747319690 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540669 | GTTTTTTAATTTTTT[A/G/T]ATAAATAAATAGGTA | 8945 |
rs747334707 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515656 | AGCTAGGGCTACAGG[C/T]ATGTACCACCACGCC | 8945 |
rs747344769 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369187 | AGTGTTTATTCAAGT[C/T]TTGGCCTTTTTTCCC | 8945 |
rs747374101 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463818 | TATATAGTGTTTAGA[A/G]GGAAAGTACTTGAAA | 8945 |
rs747410828 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101448101 | TGTCAGAAATGCACA[A/G]AATTCTGCATAGTTA | 8945 |
rs747446377 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101464244 | TCCATTTGGAAAATG[C/G]ATAGGCTGATCTGTT | 8945 |
rs747451413 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410444 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 8945 |
rs747476319 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501265 | GAAGAATGAATCTCT[A/G]TTTTTAAATTTATGT | 8945 |
rs747476984 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386784 | TGTGTTTCTTCTACT[A/G]ATAGGTGAATTGGTG | 8945 |
rs747500700 | in-del | -/TTGTT | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554426 | GTTTTTTTTGTTGTT[-/TTGTT]TTGTTTTGTTTTGGC | 8945 |
rs747515914 | in-del | -/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101455304 | CAAGCAATCCTCCTG[-/TC]TCTCTACCTCCCGAC | 8945 |
rs747526937 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101442353 | CTTAACGGGAGAGAC[-/TA]TGAGAGACATGACTG | 8945 |
rs747531155 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516845 | TCTTCTCTGTTACTG[G/T]CATTCTGGTCTTTAT | 8945 |
rs747550931 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510496 | ACCTGAGCGACAGAT[A/T]GAGACTCCATCTTAA | 8945 |
rs747552071 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101355007 | AGAAGCTAAATACTG[C/T]AATAAGGACAAGGTG | 8945 |
rs747566480 | in-del | -/CTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101437250 | CAGAAATGTTTTGTT[-/CTC]CTAATAAAATGAATT | 8945 |
rs747569292 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101462357 | TTGTTTGCTTTTTCT[A/G]GAAGAAAAGGCCATT | 8945 |
rs747569699 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481249 | GCACCCAGCCCAAGT[C/G]TACTTTATATCCTGC | 8945 |
rs747578092 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483369 | GGAGGCCGAGACGGG[A/T]GGATCACGAGGTCAG | 8945 |
rs747634392 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397113 | CCAGCCTGTCCAAAA[G/T]ATTTTAAAGTTGGGT | 8945 |
rs747635754 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101487647 | CAGCAGGTAATCCAT[C/T]TTTGGACTCCTGTCA | 8945 |
rs747637891 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502636 | CAATATAGTGATAGT[A/G]GCATCCTTCTTGGTG | 8945 |
rs747653515 | snp | A/C/G | 5.139e-05 | 0.0050688 | intron-variant | BTRC | GRCh38.p7 | 10:101521879 | CTGCCAGGTATGTCT[A/C/G]CAAGTGTTTGTAAAC | 8945 |
rs747676932 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101395116 | AATGTAGAAGTCATT[A/G]TCACTAGGTGGCATT | 8945 |
rs747705989 | snp | A/G | 5.0474e-05 | 0.00502339 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526016 | CCCTACTGAAAGCTC[A/G]GGGATTGGATCATAT | 8945 |
rs747711288 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356329 | ATCCTAATCCTGACA[C/T]TTGTGTCAGATTTAT | 8945 |
rs747735777 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425200 | TTATCCAGTCTTCCG[C/T]TGATGGGTACCTGGG | 8945 |
rs747739441 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435985 | ATTTGTTGGATTATT[C/G]CCAGTAGCTCAAATT | 8945 |
rs747774155 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453829 | ATGCTTTGGTTAAGG[G/T]TTGCCAAACTTTGTC | 8945 |
rs747786823 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419440 | TTTGAAGGTTTTATT[A/T]CGAGAAAAAGCCACT | 8945 |
rs747806497 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543840 | TTGCTACAGATTTTA[C/T]TTCTAAATATGTTAT | 8945 |
rs747812366 | snp | A/G | 6.6012e-05 | 0.00574471 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535377 | CACAAGTACTTGTGA[A/G]TTTGTAAGGACCTTA | 8945 |
rs747820607 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363024 | GATTTTGGTATCCGA[C/T]GGGAGGATCCTGGAA | 8945 |
rs747824389 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380399 | TTTTAATTAAAAAGT[A/G]AACTTTAATGTCAAA | 8945 |
rs747841828 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509554 | CCACCGCGCCCAGCC[-/T]TTTTTTTTTTTTTTT | 8945 |
rs747877380 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434863 | TGTTCTTAAACTCCT[G/T]TCTTCAGGTGATCTG | 8945 |
rs747878829 | in-del | -/TTTTGA | | | intron-variant | BTRC | GRCh38.p7 | 10:101427133 | TTTTTTTTTTTTTTT[-/TTTTGA]GACGGAGTCTTGTTC | 8945 |
rs747885055 | snp | C/T | 1.65381e-05 | 0.00287555 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430361 | GCTCTATGCCCAGGT[C/T]TCTGTGGCTGGGCTG | 8945 |
rs747886305 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531874 | CATACATAGCAGTGT[A/G]ACTGGTAAACTTGTA | 8945 |
rs747903177 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101405150 | CCCCAGTACTATCTG[C/G]TTCCCTGGGGCCGCC | 8945 |
rs747923201 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101458548 | ATTGATACAGTGTTA[C/T]TAGTTCACCTACAGA | 8945 |
rs747940371 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394016 | ATTGAGTCTGTACCT[A/G]GGACTTCCAGGGCTT | 8945 |
rs747952717 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551476 | CCACTCAAGTCTCCA[A/G]CCTCTCTCTCAGGCA | 8945 |
rs747959181 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428214 | TATTTGAACAAAATA[C/T]CAAGGTAGGTAGTTA | 8945 |
rs747960760 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101420520 | TCCCCCCACCCTCCA[C/G]TGCCCTGTGTGGATG | 8945 |
rs747960816 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404338 | CCCAGCCAATCCTAG[C/T]TATATTACAGTCTTT | 8945 |
rs747965553 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101500865 | GGGGTTATAGAATAT[C/T]TTGCTTGCCCAAATA | 8945 |
rs747970322 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527096 | GTGACATATTAAATA[C/T]TCTCATTGACAGAAA | 8945 |
rs747972339 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511346 | AATCTCAGCTCAGGT[G/T]TCACTTCCTTTAGAG | 8945 |
rs747982210 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363956 | CATCTTACAGTGATA[A/G]GTATTTATTCTCTTG | 8945 |
rs748018550 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530020 | TAACTTCCGGATGAG[A/G]AATTAAATTTTTTAC | 8945 |
rs748065927 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483323 | AAAATGGCCGGGCAC[A/G]GTGGCTCACACCTGT | 8945 |
rs748118847 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497469 | ACTTTGGAATGCCCA[G/T]GTGGAAGGATTGAGC | 8945 |
rs748135600 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101443706 | GAGATTGAGGTACTT[A/C]GATTTCTTGTATGAA | 8945 |
rs748140088 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414193 | GACTACTCTAGGTAA[C/T]TCATATAAGTGGATT | 8945 |
rs748141251 | snp | A/T | 1.73027e-05 | 0.00294127 | intron-variant | BTRC | GRCh38.p7 | 10:101532448 | GTGAGGTCTATTCAG[A/T]TGTAGAAAGGTAGCA | 8945 |
rs748142693 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101534111 | CCACACTCTGCTGTG[A/G]AGCCCATATTTACAA | 8945 |
rs748161822 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459381 | CCTAGTAATCTCATT[C/G]ACTGGCATTCTGCTT | 8945 |
rs748166958 | snp | C/G | 0.0136203 | 0.0813918 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538322 | GGGATCTTGTGGCTG[C/G]TTTGGACCCCCGTGC | 8945 |
rs748217748 | snp | C/T | 1.74211e-05 | 0.00295132 | intron-variant | BTRC | GRCh38.p7 | 10:101532261 | GATTCTAGGTGTTTC[C/T]TAACACTGCCTCTTT | 8945 |
rs748222747 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517233 | ACAGGTGTCAGCTCC[C/T]TCTGTGTATATAAAA | 8945 |
rs748222856 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366196 | GTACTTGGCAATAAA[A/G]TATAGGAAAAAAAAA | 8945 |
rs748265778 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101535870 | TCCTTTTTGGGGTTT[G/T]CCCTTCACAAAGATG | 8945 |
rs748288591 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101529015 | GCTCAGTAATGGTAA[-/CT]CTTAAAAGTATAATA | 8945 |
rs748294153 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392729 | GGGTTTCACCATGTT[A/G]GCCAGACTGGTCTCG | 8945 |
rs748297556 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101399409 | GTCATGTATGACTCA[C/T]GACTTAGGTCATACA | 8945 |
rs748312289 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453131 | AATTTATATTTGGAA[C/G]CTAAATTAGCTCCAA | 8945 |
rs748323726 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490675 | TAGCAAATGTTATTT[G/T]CTCATCTTCCTCCTC | 8945 |
rs748327288 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372592 | CAGCTAGGCCGGTTG[C/T]GGTGGCTCACACCTG | 8945 |
rs748357923 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506191 | GTGCTGGGGTTACAG[A/G]CGTGAGCCACCTGTA | 8945 |
rs748360190 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381804 | AGAGTTGCAGACATG[A/G]TATTTTACCTTCTGC | 8945 |
rs748365014 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101524210 | CCTATATCTTTTGTT[-/A]AAACAGAATAGATTT | 8945 |
rs748378251 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415931 | TTGCCTACAGTATTC[A/G]GTACAGTAACATGCT | 8945 |
rs748390277 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353865 | ATCAGCCGATTTCCT[-/C]TGCGTAATGGCAACT | 8945 |
rs748401277 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101359227 | AGATGTTTCACTGTA[A/G]TGGAATTTTCTTTAC | 8945 |
rs748412573 | snp | C/T | 1.79219e-05 | 0.00299344 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521650 | ACAGACAAAACTTGC[C/T]AATGGCACTTCCAGT | 8945 |
rs748439018 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101468106 | GAGCAATTTAATAAC[C/T]GGCTTTCTTAAAATT | 8945 |
rs748453515 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528989 | CTTGAATAATACTGA[A/G]TATGCTGTCTGCTCA | 8945 |
rs748457779 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101384000 | CGGTACCACAGGCTT[C/G]TATCACCATGCCCTG | 8945 |
rs748461088 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459391 | TCATTCACTGGCATT[C/T]TGCTTCTACTCTTTA | 8945 |
rs748487370 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491864 | CGGAGAAAAGGCTTG[A/G]GACAGGGATGAGTGA | 8945 |
rs748543257 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101454343 | TTAAAATTTAGTTAG[A/G]GAATTTCCAGTAGAG | 8945 |
rs748568319 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101546114 | TTTAGCAGTACCATC[A/C]ATCAAGTGGATATAA | 8945 |
rs748572060 | snp | C/T | 1.65682e-05 | 0.00287817 | intron-variant | BTRC | GRCh38.p7 | 10:101479476 | AGTAATATTGCTCAT[C/T]AATGTATATTACACC | 8945 |
rs748574288 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101522780 | CCTATTTTTACCCAT[A/G]CATAGGTCCAAATAA | 8945 |
rs748580477 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101382327 | AAAAAATCCAGGATC[C/T]AATCATGTTATATAT | 8945 |
rs748592284 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424605 | ATTCAGCTTTCGTAT[A/G]GTAAATGCTGAGGCT | 8945 |
rs748593003 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101393918 | AGCAGTTGAATGAGA[A/C]AACTAATCTTTCAAA | 8945 |
rs748605222 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101454617 | AACCCCTGTATCTAC[-/A]AAAAAAACAGAAAAA | 8945 |
rs748617811 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434153 | TTCTGCACTCAATCT[A/G]TTGTGGTTTGTTATT | 8945 |
rs748628556 | in-del | -/TTCC | | | intron-variant | BTRC | GRCh38.p7 | 10:101379016 | ACTTACAAGATCTCT[-/TTCC]TTCCTTCTCTCTTGG | 8945 |
rs748631344 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515411 | ATCTTAATAGATCCA[A/G]TTTCTGAATACAGTG | 8945 |
rs748645280 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101439250 | GGATGTGTGCCTGAG[C/T]GCTTCATCCTGGGCT | 8945 |
rs748680421 | snp | C/T | 1.65921e-05 | 0.00288024 | intron-variant | BTRC | GRCh38.p7 | 10:101533117 | GAAATATCAGCTCTG[C/T]TCTGTTCTTTGTCAT | 8945 |
rs748688605 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386647 | ATGAGCACATGAAGA[A/G]CCAAGGACTTGTTTG | 8945 |
rs748688839 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368321 | TTACCAGGAGCAGAT[A/G]CTAGCACCATGCTTC | 8945 |
rs748703752 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431070 | TCCCCTCAGCCTTTC[-/T]TTTTTTTTTTTTTTT | 8945 |
rs748707446 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460934 | TTGAGACGGAACCTT[C/G]CTCTGTCACTCAGGC | 8945 |
rs748733991 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423888 | AGAAGCCTATTCCTG[C/G]TGATGATGCCATTTA | 8945 |
rs748748819 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394085 | TGTTTAGCTAAAAAG[A/G]GATATTTCCATCTCA | 8945 |
rs748748952 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410305 | GATTTTCATTTTCCC[A/G]ATGACCGCTGATGTC | 8945 |
rs748787959 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555159 | GTAAGGATTTTGCTA[C/T]AGATGAAGGTAGAGG | 8945 |
rs748788880 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101499750 | CTACGAGATTGCTCA[C/T]TATCAAAAAATGCTA | 8945 |
rs748789800 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534895 | TGTTTCTGCATCTGG[A/G]GATAGAACTATAAAG | 8945 |
rs748803908 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408688 | CATTTTATGCCTTCT[A/G]TTGGCTTACTAGGTA | 8945 |
rs748840698 | snp | G/T | 1.66112e-05 | 0.00288189 | splice-acceptor-variant | BTRC | GRCh38.p7 | 10:101535353 | CCATTTTCTTTTTCA[G/T]GTATGGAACACAAGT | 8945 |
rs748848043 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369087 | ATGGTACTATCCCAC[C/T]GTTTTAATTTGTGTT | 8945 |
rs748875054 | snp | A/G | 3.31252e-05 | 0.00406958 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521689 | GCCCAAGCAACGGAA[A/G]CTCTCAGCAAGCTAT | 8945 |
rs748875370 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506103 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 8945 |
rs748908406 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394951 | AATGCTAGGACATGC[A/G]TGCACAGATAATTCA | 8945 |
rs748909684 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101483237 | AAAACAAATTACAAC[A/C]ACCCTAAGTTGGCAA | 8945 |
rs748935882 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101509244 | CAGTGGCAATGTGGA[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8945 |
rs748961071 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101413957 | ATCACATTGGGGGCT[A/G]TTGTTTTTAACTGTG | 8945 |
rs748977982 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101370060 | ATTTGGACTTCAACA[-/CT]CTGTGCAGGGCTGCC | 8945 |
rs748982725 | snp | A/G | 1.70136e-05 | 0.00291659 | intron-variant | BTRC | GRCh38.p7 | 10:101430311 | GCCATCCTGTCTCAT[A/G]CTGTCCCATCTCATA | 8945 |
rs748988248 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538823 | GAGGTCAAGGCAGAT[A/G]GATCACCTGAGATCA | 8945 |
rs749019687 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500883 | GCTTGCCCAAATAAT[A/G]TTGTGAAAAATGTTT | 8945 |
rs749025369 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101508696 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCA | 8945 |
rs749040474 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485767 | GGAGCTAATAGGCTC[C/G]AGCTTGTCTTTGTGG | 8945 |
rs749050770 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525822 | ATACTGTTCATTTCT[C/G]TAACCTTATGGAAAA | 8945 |
rs749052444 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419198 | ATATTTTTAGTAGAG[A/T]CAGGGTTTCACCATG | 8945 |
rs749068098 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524215 | TATCTTTTGTTAAAC[A/G]GAATAGATTTTTGCC | 8945 |
rs749088104 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453344 | TTATAATCCACCACA[A/G]TTTACCTGCTTTGCT | 8945 |
rs749094508 | snp | A/G | 1.74824e-05 | 0.0029565 | intron-variant | BTRC | GRCh38.p7 | 10:101532246 | GCCTAAAAAGAGTTT[A/G]ATTCTAGGTGTTTCC | 8945 |
rs749105890 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379038 | CTTCTCTCTTGGAAT[A/G]TTGACTATAAATTTC | 8945 |
rs749112747 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434759 | GAAAAACCACTGCTT[A/G]AGAACAGCCTGACCA | 8945 |
rs749112915 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101417672 | AAACTTACAGTTTAT[A/G]TTTTGTTTCATTTTA | 8945 |
rs749142905 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | BTRC | GRCh38.p7 | 10:101536664 | GATGGGTGAGTGTGC[C/T]AACAGAGTGTAAAAA | 8945 |
rs749143989 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556609 | GTGTCAACATAGTAT[C/T]GGAAAGAGAGCCATT | 8945 |
rs749155092 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101512281 | AATCATTATATCCCC[C/T]TTCCCCCCATAGTTC | 8945 |
rs749229092 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404121 | CTGCAAGCTCCGCCT[A/G]CCGGGTTCACGCCAT | 8945 |
rs749229292 | in-del | -/G | | | intron-variant, frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354411 | TGCGGAGCGGACCCA[-/G]GGGTGGGGGCAGCGG | 8945 |
rs749255290 | snp | G/T | 1.68244e-05 | 0.00290033 | intron-variant | BTRC | GRCh38.p7 | 10:101531216 | CATGATTTTCACTGG[G/T]AAATATTTGTTATTT | 8945 |
rs749258613 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533732 | ACCTAGGAAAAAAGC[A/G]GTTAAGTGCATTGTT | 8945 |
rs749260186 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101391406 | AATATAGTATTGTTT[G/T]CAAATAAAATTCTTT | 8945 |
rs749262212 | snp | G/T | 1.64784e-05 | 0.00287035 | intron-variant | BTRC | GRCh38.p7 | 10:101538271 | TTTTAACTAACATTT[G/T]TGTCCCCTTTTTGAT | 8945 |
rs749262230 | snp | C/T | 3.30033e-05 | 0.00406209 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479445 | TATGAAGACTGAGAA[C/T]TGTGTGGCCAAAGTA | 8945 |
rs749278864 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473124 | GTCCCACACAGTGAC[-/T]TAAGACCGATCTTTT | 8945 |
rs749281282 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457041 | GTTTTTTCCTATGGA[C/G]ACATACCTATGATAA | 8945 |
rs749284575 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549822 | CTGGGAACATTCTAC[A/G]TCTTCATCAGGGTGG | 8945 |
rs749303107 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101473384 | TGACCTTCTGGGCTC[A/C]AGCAACCGCCCACCC | 8945 |
rs749341717 | in-del | -/AGT | | | intron-variant | BTRC | GRCh38.p7 | 10:101360866 | CGCAGCTCTGCCATC[-/AGT]AGGCTGAGCTCCCTG | 8945 |
rs749345356 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551202 | GTTTGAAAACTAAGT[A/G]CTGTAATGACCCAAA | 8945 |
rs749349631 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481919 | TCAGATTTGAGCCAA[A/G]TAATCAGTTGGTCAA | 8945 |
rs749433377 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101442006 | TTCTTTGATTTGAAT[G/T]ATGGAAAAATTTCTA | 8945 |
rs749441017 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389782 | GGTGCACGCCACCAT[A/G]CCTGGCTAATTTTTA | 8945 |
rs749461949 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412242 | ATAATTCATTCTTCA[C/G]TATTCTGCCTCACTA | 8945 |
rs749496300 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534701 | ATGCTAAACACGTTG[A/G]TTCACCATTGTGAAG | 8945 |
rs749568837 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518742 | CACCCAGGACCTAGG[A/G]TCTCAAAATTTCCAT | 8945 |
rs749584038 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101534521 | TAAGGACACACTGGC[-/A]GCATCCCATCCCCTT | 8945 |
rs749592275 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362548 | TTACAGGCATGCGGC[A/G]CCACACCCAGCTAAT | 8945 |
rs749603546 | in-del | -/CA | | | intron-variant | BTRC | GRCh38.p7 | 10:101418989 | ATACATGTAACATCT[-/CA]CAGTTTCTTTTCTTT | 8945 |
rs749622736 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399207 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 8945 |
rs749657472 | snp | A/T | 1.67435e-05 | 0.00289335 | intron-variant | BTRC | GRCh38.p7 | 10:101550899 | TTGCCCAGGTATCGA[A/T]ATCGATTATGTACAT | 8945 |
rs749661772 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519171 | GCAATCTCCACCTCC[A/T]GGGTTCAAGTGATTC | 8945 |
rs749678008 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398284 | TATCTAAAAATGTGT[A/G]TTGAAAATTTCTTTT | 8945 |
rs749700306 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101467788 | TAATTTTAGTCATCT[A/G]TTTTAATTACCTATT | 8945 |
rs749700381 | in-del | -/ATTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101491385 | CACTTAAACTTGGTT[-/ATTA]ATTTTGTCAATTAAA | 8945 |
rs749700758 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475045 | AATATTTATGTTTGT[A/G]TGTGTATGAATAGTA | 8945 |
rs749715654 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101399324 | AACTAGAATCACCTT[-/TTT]TTTTTTTTTTTTTTT | 8945 |
rs749763765 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385130 | CCCAGCTACTTGCTT[G/T]GAGGCTGCAGTGGGC | 8945 |
rs749788504 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101382144 | CCTGCCACCACGCCC[A/G]GTTAATTTTTGTATT | 8945 |
rs749807379 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452964 | AGTTTTCCCCATTGT[A/G]TCCTAAAAGGATTAA | 8945 |
rs749812008 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489540 | TGATGTAAAAAGATC[A/G]CTTACAAAGCTTGTG | 8945 |
rs749819262 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101457178 | AATATCTTACTGTAC[C/T]GTACTCACCCTTCTT | 8945 |
rs749830869 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490410 | GATTCTCATGTGAAC[C/T]TGGTGAGATGGACTG | 8945 |
rs749856391 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545940 | CAATCCTTAATGTGT[A/G]CACACCTAACAACAG | 8945 |
rs749863425 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101440790 | GAAAGGCAAGAGCTG[C/T]TCTGCATCAGTCTAG | 8945 |
rs749892090 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460859 | ACCCTCCTGTTAGAA[C/T]GTTATGACTATATGT | 8945 |
rs749894652 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101548166 | TGGCATGACTTTTAA[A/G]AAATTGTTTCATAGT | 8945 |
rs749923466 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496484 | GCATCAGCGCAATCA[C/T]AGCTCACTGTAACCT | 8945 |
rs749963473 | snp | A/C | 1.7814e-05 | 0.00298441 | intron-variant | BTRC | GRCh38.p7 | 10:101414730 | CTGTGGGCCTAGGCT[A/C]ATGTAATGTGTGTGT | 8945 |
rs749970990 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493435 | GCCCAAGGTCATACT[C/G]TATGTTGCAGAACTG | 8945 |
rs749994607 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515256 | CACCACACCTAACCG[-/T]TTTTTTTTATTTTCA | 8945 |
rs750015432 | snp | A/G | 1.65534e-05 | 0.00287688 | intron-variant | BTRC | GRCh38.p7 | 10:101532912 | TCTCCACAGCACCCC[A/G]TCATCACATTGATCA | 8945 |
rs750034706 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435835 | TTGACAAATATGTTA[A/G]TGAAATGTCTCATTT | 8945 |
rs750045304 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101378521 | GGCTCCCAATTATAA[-/TTT]TTTTTTTTTTTTTTT | 8945 |
rs750059167 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425340 | AAGGCTAGTGAAGTC[A/G]TTCAGTTGGATAACA | 8945 |
rs750072858 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383393 | TTCTATAAGTCTTCC[-/T]TTTTAAAAAAAAAAA | 8945 |
rs750093509 | in-del | -/C/CTTCG | | | intron-variant | BTRC | GRCh38.p7 | 10:101472323 | CTTCTCTTCTCTTCT[-/C/CTTCG]CTCTCTTCTTTCTTT | 8945 |
rs750095182 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540112 | GTGTCTTTCAAAAAG[C/T]GGTTCTTAATTTTAA | 8945 |
rs750131216 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101494842 | TTACAGCATCACATC[C/T]AAATTATACTTTCTG | 8945 |
rs750131887 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387908 | TTGGTCAGGCTGGTC[C/T]TGAACTCCTGACCTC | 8945 |
rs750140991 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517164 | TTTTTAGTCTGTATC[A/G]TAGGCAACAGTGGCA | 8945 |
rs750147596 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556383 | ATACTGGAAATAATC[A/C]GGGCAATTTTTTTCT | 8945 |
rs750151232 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512865 | ATAAACAAAAAAGAA[A/G]AGGGAGATGTGCAGG | 8945 |
rs750163906 | snp | A/C | 2.61558e-05 | 0.00361624 | intron-variant | BTRC | GRCh38.p7 | 10:101521626 | TTATGTTTCTTTTAA[A/C]CCCCTTCTACAGACA | 8945 |
rs750177053 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101394751 | GCCTGCAGTTCCCTG[A/T]AGAGTAGTACATGGC | 8945 |
rs750232166 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356085 | GTGCAGTGGTGCAGC[C/T]TCCGCCTCCTGGGTT | 8945 |
rs750283452 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369790 | TAATACCACAGGGTT[C/T]GTTCGATAATTTCAT | 8945 |
rs750286519 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409999 | TGCCAAATTGTTTCC[C/T]GTGGTTACTGAACTA | 8945 |
rs750288508 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101426861 | GTATGGTTAAAAGTG[C/T]CGCCTGCCCTCTTGT | 8945 |
rs750291053 | snp | A/C | 9.8912e-05 | 0.0070318 | intron-variant | BTRC | GRCh38.p7 | 10:101538249 | CCCTGCCTTCTCTTA[A/C]ATTTGCTTTTAACTA | 8945 |
rs750296813 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488336 | TTCTATTACCTGTGC[A/T]ATTGACTTCTCAGTG | 8945 |
rs750350256 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484883 | TTACAGAGATATACA[C/T]AGTTAAATGACTTTT | 8945 |
rs750350323 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101452706 | GCACTGTGCTTGGAA[C/T]TGGTATATTACTAGA | 8945 |
rs750351066 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514949 | TGTGGTTTTTTAGGG[-/T]TTTGTTTGTTTTGTT | 8945 |
rs750359652 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101396883 | TCTTGGCTCACCGGA[A/G]CCTCCGCCTCCCGGA | 8945 |
rs750363572 | snp | A/G | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534809 | GCCTCCCCAACTGAC[A/G]TTACCCTCCGGAGGG | 8945 |
rs750374853 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450911 | TAAGGCAGATTTCTG[C/T]TTGTTATTAATATAT | 8945 |
rs750374889 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434721 | ATTGCTTAAGCCCAG[C/G]AGTTCAGGGCTATAG | 8945 |
rs750382155 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101541030 | TTCTGATTGTTCATT[A/G]CAAATACATAGAAAT | 8945 |
rs750390029 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101501934 | TCTAGGTTAAACAAA[C/T]AAACAAACCATTTTT | 8945 |
rs750415340 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557258 | ATGGAGTGTGTTTTG[G/T]GTTTTTTTTAACTGT | 8945 |
rs750430574 | snp | A/C | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514835 | TTCCTTTCCATTGAT[A/C]TACACTTGTGTCCTT | 8945 |
rs750438172 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101482627 | GTCTTGATCTCCTGA[C/T]GTCGTGATCCGCTTG | 8945 |
rs750493005 | snp | A/G | 0.000101631 | 0.00712778 | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354252 | ACGGTGGAGGCCGGG[A/G]AACGGTGGAGGCGCT | 8945 |
rs750496767 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101529223 | ACATAAAGACAGAAG[A/C]CAGTTTTCAGTACCT | 8945 |
rs750503328 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101381088 | GGGGGTGCATGACTG[C/T]ATTTTTACTTATTCT | 8945 |
rs750508444 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380034 | TTGTTTATAACTGAC[A/G]ATACGAGAATTCTAC | 8945 |
rs750527046 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472988 | CTGAAATCAGAAAGC[C/T]GCTAGTTTTCACAAA | 8945 |
rs750536305 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101435443 | TACTTCATATAAATG[C/T]CATCATATAGTGTAC | 8945 |
rs750568452 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534669 | CTTCCAGAGTGTGGG[A/C]TGTAAATACAGGTGA | 8945 |
rs750589885 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101395896 | CCTTAAATAGTAGTA[A/G]TATTTCCATGTTTTG | 8945 |
rs750616285 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497139 | GTGTGATACCCAGTT[A/G]ACCTAGCACCATTTA | 8945 |
rs750626654 | snp | A/T | 3.31559e-05 | 0.00407147 | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550869 | CAGATAAATAACCAT[A/T]CACTGACCTCATACT | 8945 |
rs750657361 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101531102 | CTTGAACCCAGGAAG[C/T]GGAGGTTGCAGTGAG | 8945 |
rs750719046 | snp | A/C/T | 6.61117e-05 | 0.0057491 | intron-variant | BTRC | GRCh38.p7 | 10:101536522 | ACGTGAAAATTCACC[A/C/T]GACTTAATTTTCTCT | 8945 |
rs750720950 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392548 | GTTGCCCAGGCTAGA[A/G]TGCAGTGGCGGCATG | 8945 |
rs750727121 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101372033 | TTCTTTTTCTATTGC[A/G]GGGTCATTTTTGTCA | 8945 |
rs750728501 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555009 | CCCAGTATAATGATA[-/C]ATCGTAGCCTAAGAA | 8945 |
rs750731729 | in-del | -/T | 1.64868e-05 | 0.00287109 | frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521829 | ACATAAACTCGTATC[-/T]TAAACCTATGTTGCA | 8945 |
rs750735634 | snp | C/G | 7.02753e-05 | 0.00592729 | intron-variant | BTRC | GRCh38.p7 | 10:101525999 | TTTTCTTTGCCTCCT[C/G]CCCCTACTGAAAGCT | 8945 |
rs750737701 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101552970 | CCCTGCCTTTAGTAT[A/C]ACTTCCCCCATCAGG | 8945 |
rs750777812 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428871 | GGATCTTGCTGTGCT[C/G]CCCAGGCTGGATTTG | 8945 |
rs750789238 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483082 | AATACTATTTATTTC[C/T]CTAAAAGCAGCAATG | 8945 |
rs750791520 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101357834 | GAAAAAAGTTTAAGC[-/A]GAATGTTTAACTTTT | 8945 |
rs750803110 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101397531 | TCAATTTTATTGCCT[C/G]AGATCATAATTGTGC | 8945 |
rs750817083 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362454 | AGGTTGGGGTGCAAT[A/G]GCACAATCTCGGCTC | 8945 |
rs750890787 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101552080 | TGCCATTTTTAATAT[C/T]CTTCCTGACTCTCTG | 8945 |
rs750895737 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101549331 | CACTACTTGGGAGGC[G/T]TAAGCAGGAAAATCA | 8945 |
rs750905238 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354479 | GGAGCTTAATCGAGG[A/G]GGGGGCTCCAGGCGG | 8945 |
rs750906635 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101521126 | AAATGTTAAAAATTA[A/G]CAGGACATGATAGTG | 8945 |
rs750954027 | snp | A/G | 1.72311e-05 | 0.00293518 | intron-variant | BTRC | GRCh38.p7 | 10:101535486 | AGGTGAGCAGCAAGT[A/G]CCTTGTATCATAAGG | 8945 |
rs750979202 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400528 | AGAGGAAGATGATCC[A/G]TAAGTCTAATGCTAA | 8945 |
rs750986052 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365047 | TGATTTTAATTCTTT[C/T]TCTTTTTTTCTTTTT | 8945 |
rs750990897 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483742 | GATTTGTGTTTGGAG[C/T]ATGATGAGCTCTGTG | 8945 |
rs751026062 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360456 | TCAACTCACTGCAAC[C/T]TCCGCTTCCCAGGTT | 8945 |
rs751049973 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545780 | GCACCCCTAGCCCTG[A/G]TGGACCATTCTAACA | 8945 |
rs751064089 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517262 | AATGGCCTAATGCCA[-/T]TCTTGAAAATATGCT | 8945 |
rs751070470 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425135 | GACATGATTTCATTA[-/T]TTTTTTATGGCTACT | 8945 |
rs751084990 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452548 | GGATGCATCTGTAGT[A/G]TTATATGATTAGTGT | 8945 |
rs751086036 | snp | C/T | 1.65729e-05 | 0.00287857 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531304 | TCTTTTTATAGAGCA[C/T]TTTATCCTAAAATTA | 8945 |
rs751125628 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101455060 | TTCAATCCAAGAAAC[-/T]TTTTTTTTTTTTTTT | 8945 |
rs751161172 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493150 | TAAATGGTCTTATTA[C/T]AGAGTTTGTATAGGA | 8945 |
rs751194181 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101529773 | ATATAACAGGGAGAG[A/G]GCAGGGGAGAAACAC | 8945 |
rs751194948 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476362 | GTAAGTTCTGTACTT[C/T]ATATAGTACCAAGTT | 8945 |
rs751227548 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101388412 | TGCCCAGCTGTTCTC[A/G]AACTCTTGGCCTGAA | 8945 |
rs751229147 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491530 | TGAAACCCAGTTTCT[A/G]CTAAAACTACAAAAA | 8945 |
rs751230343 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101390335 | GATGTCCTGGTATGA[-/TTT]TTTTTTTTTTTTTTT | 8945 |
rs751251822 | snp | A/G | 1.65671e-05 | 0.00287807 | intron-variant | BTRC | GRCh38.p7 | 10:101462080 | AATTCAGCCTTACTT[A/G]AAATAAAAAGCTACC | 8945 |
rs751264282 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425123 | ATGTTCTGCAGAGGA[C/T]ATGATTTCATTATTT | 8945 |
rs751267686 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101545051 | ATGAGACCCTGTCTC[-/A]AAAAAAAAAAAAGAA | 8945 |
rs751269139 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492453 | GAGTGCTTTTATTTA[C/T]ATCTATGTGTGACGT | 8945 |
rs751295596 | snp | C/T | 4.94947e-05 | 0.00497443 | intron-variant | BTRC | GRCh38.p7 | 10:101534647 | ACCATCTAAATCTCA[C/T]CTATCACTTCCAGAG | 8945 |
rs751322959 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408169 | GTGCTCAGTAGCCGT[A/G]TGTGACTAGTGGTTA | 8945 |
rs751325348 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433895 | TTATTGAGGACCCCA[A/G]AGTGCTTTTGTTTAT | 8945 |
rs751357252 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496009 | GGAATCATATAGTAT[-/T]TTTTTTTTTTTTACT | 8945 |
rs751373171 | snp | C/T | 3.31192e-05 | 0.00406921 | intron-variant | BTRC | GRCh38.p7 | 10:101461937 | TCCCAAAGGATAAGA[C/T]TGAAGATAATGAGAA | 8945 |
rs751392046 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368117 | TTATGGAGGTGCGTT[C/G]CTCATGAAGGGCTTG | 8945 |
rs751408849 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385545 | ATTTAAGAGTCTAGA[A/G]GGACCATCTAATTCA | 8945 |
rs751423600 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101409865 | ATTTTGAATAATGCT[A/G]CTATGAACATGTGTA | 8945 |
rs751423817 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101478418 | ATTGAGATTCTTTTA[C/T]AAAAATATTTCATGA | 8945 |
rs751437558 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447222 | ATGACCTCTGTTATT[C/G]TTGAAACCTATCCAG | 8945 |
rs751440920 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500427 | ACATGGTGCATGACT[A/G]TACTTTGATTTGGCC | 8945 |
rs751445100 | in-del | -/TCTCTCTCTCTCTCTCTCTCTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101442264 | AATTGAATTAGAATC[-/TCTCTCTCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 8945 |
rs751446921 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101355735 | GAATTTTAGACTTTA[A/T]ACTGCCCCATTTATA | 8945 |
rs751492500 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405680 | AATAGTTGTTCTATA[C/T]GTTCTGTCCATTTCT | 8945 |
rs751498219 | snp | C/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354134 | GCTGCGGCCTGGCAC[C/G]AAAGGGGCGGCCCCG | 8945 |
rs751505095 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554857 | CTCCCCAGGCAAGAA[A/G]GTATCCTCTTCCCAA | 8945 |
rs751554930 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101507999 | TTTAGAACAAAAGAA[C/T]CTATCACCCTGGAAG | 8945 |
rs751565597 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101499391 | ACCATGCCCAGCTAA[A/T]TTTTTTTGTATTTTT | 8945 |
rs751579333 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482489 | CAAGCTCCGCCTCCC[A/G]GTTTCACGCCATTTT | 8945 |
rs751603535 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526096 | GAACTTGTGTGCAAG[A/G]AATGGTACCGAGTGA | 8945 |
rs751622416 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538287 | TGTCCCCTTTTTGAT[C/G]TTTAGAAAAATTAAA | 8945 |
rs751627103 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378107 | TTTTAATAATTCTTA[C/T]TCAGGGAAGTAATTT | 8945 |
rs751629385 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555623 | CCAGAGAAGGTAAAC[C/G]CCACTTACCATCTCT | 8945 |
rs751713820 | in-del | -/TCC | | | intron-variant | BTRC | GRCh38.p7 | 10:101429526 | CTCCCCTCCCTCCCT[-/TCC]TCCTCCTCCTCCTCC | 8945 |
rs751734944 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526464 | CCTCCTGTTTAAAAC[A/G]TTCTGTTATCTGGGC | 8945 |
rs751755426 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101423741 | ACTTAAGGGATCTAG[-/A]TACAATGCCTGGCAG | 8945 |
rs751756890 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528845 | TTCTACTAACCAAAA[A/G]TAGTAAGTAAATACA | 8945 |
rs751769503 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452089 | ATCTCAGTAAATTAT[A/G]ATCCTGTTTTTCATT | 8945 |
rs751782246 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510617 | ATCTCTTCCTTTCCC[C/T]CTCAAAATCCTTGTA | 8945 |
rs751794785 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371406 | GGTCTTGAACTCCTG[A/T]TCTCAGGTGATCCGC | 8945 |
rs751796602 | snp | A/G | 3.86967e-05 | 0.00439851 | intron-variant | BTRC | GRCh38.p7 | 10:101525977 | CATTCGCCACCTTCT[A/G]TGTTCTTTTTCTTTG | 8945 |
rs751802825 | snp | A/G | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557324 | GTGAATTTTCTAAGC[A/G]TCTTGTCTCCTTGCC | 8945 |
rs751805541 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456445 | TCTGAGGATTTAAGT[C/G]TAGGATAAAAAGAAA | 8945 |
rs751826491 | in-del | -/TATATATATACACATATATATATATGTATATGTGTATATATATATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101505117 | GAGTATATATTTATA[lengthTooLong]TATATATATGTGTAT | 8945 |
rs751829547 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488294 | TCCTTTCCTGATTCT[G/T]TTTATTAGAAATTTG | 8945 |
rs751837147 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101495117 | CAGGGTTCTCCTAAT[A/G]CTGACCTACTTTGCT | 8945 |
rs751868338 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404643 | AGATATATTCCATGC[A/G]TGTGCCACTTGATGG | 8945 |
rs751914934 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363626 | ACCACGCCCGGCTAA[A/G]TTTTGTATTTTTTAG | 8945 |
rs751922079 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499624 | AGAATATACCCTCCA[A/G]AATGTCTTGATTCTG | 8945 |
rs751925099 | snp | A/G | 1.68485e-05 | 0.00290241 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535468 | TCATCTGACAACACT[A/G]TCAGGTGAGCAGCAA | 8945 |
rs751980367 | snp | A/G | | | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534905 | TCTGGGGATAGAACT[A/G]TAAAGGTAATAAGGC | 8945 |
rs752026690 | in-del | -/CGCGGC/CGCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101532802 | GTGCGCGTGTGCGCG[-/CGCGGC/CGCT]CGCGCGCGCTTAGCT | 8945 |
rs752064227 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502555 | TACTTTGGTTCTTAA[A/G]TTTTTGCATACCAAT | 8945 |
rs752073968 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470152 | TTTTAAAAATTGCAT[G/T]GTTTGCCTTTTTATT | 8945 |
rs752077302 | snp | A/G | 0.000181562 | 0.00952617 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430435 | AACCCAGGGACTGGC[A/G]CACTCACAGCTTTCC | 8945 |
rs752088530 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444776 | GAAAACAAAAAATCT[G/T]AAGGAGATAAATTAT | 8945 |
rs752090301 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427334 | TGTTGGCCAGGATGG[C/T]CTTGATCTCTTGACC | 8945 |
rs752101183 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519919 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 8945 |
rs752122516 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551679 | CGGAAGTACATGTTC[A/G]CTACACGTTTCTGCA | 8945 |
rs752131599 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373529 | ATCAAAGCAGTAGGT[A/G]GGTAAGGGAAAATGA | 8945 |
rs752159963 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101466759 | AATGACTGTGTTGTC[A/G]TCTTCTGTTAATGAC | 8945 |
rs752167002 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532589 | TCATTTCCTTAAAGG[A/G]CAGACATCAGCTTCC | 8945 |
rs752167030 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496986 | AATTAGTGTTTTTAC[A/T]TTCTACTTAAGAAAT | 8945 |
rs752172450 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101483603 | GTCTCAAAAAAAAAA[A/C]TGAAAATGTAGGAGG | 8945 |
rs752199397 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536567 | CATAGAATGTGGTGC[A/G]TGTTTACGAGTGTTA | 8945 |
rs752219063 | in-del | -/GCACCAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101450564 | GTTCCAGTATAACAG[-/GCACCAAT]GCTGTTTGACTTGAA | 8945 |
rs752270379 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441602 | AGTTTTTTCTTGGCC[A/G]GGCGTGGTGGCTCAT | 8945 |
rs752274670 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416918 | TTATGACCAAAAGCA[A/G]AATCCCAGTATGTAT | 8945 |
rs752289487 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101371986 | TTTCTTTCTATAGCC[A/G]GCTTATTCAGCACTA | 8945 |
rs752306694 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487989 | GTTGATATATTAATA[A/G]TCTATAGACTGTAAT | 8945 |
rs752314384 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411919 | AACTTGATGCTCTTG[C/T]GGCTGATTTTAAGCT | 8945 |
rs752319865 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398697 | TCATCCTTTGCCCTT[C/T]AGTGGAGGATTTTAT | 8945 |
rs752321458 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428553 | CCCTTCTTTTGAAGC[C/T]CAGTGTCCACTTTAT | 8945 |
rs752322400 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364820 | ATTTCTTTTAATTCT[-/T]TTTTTTTTTTTTTTG | 8945 |
rs752335371 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452072 | CATAGAGAATTGCTC[A/G]AATCTCAGTAAATTA | 8945 |
rs752337728 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490118 | CATTTTTTTTTCAGG[C/G]TGTGTTTCCATATAA | 8945 |
rs752361392 | snp | A/C | 1.65124e-05 | 0.00287331 | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101462037 | TAGGAAGATAATACC[A/C]GAGAAGAATTCACTT | 8945 |
rs752361697 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485867 | AAGAGGGATGAAAGA[A/G]GAAAGTTCTTCATCA | 8945 |
rs752361838 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101518212 | CCACCGCGCCCGGCC[A/G]AAGTAGTGTCTTAAT | 8945 |
rs752366731 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532968 | TCTGGGATAAAAACA[C/T]ATTGGAATGCAAGCG | 8945 |
rs752375706 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380308 | AGAGCAAATATTTTG[C/G]AAATTATAAAGGACT | 8945 |
rs752378644 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101526804 | AAGTGGAATAAGAAC[-/T]TCTAGCCATCAGAAA | 8945 |
rs752381156 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546513 | AAATAAAAATGAAAA[C/T]ACAGCTATCAAAATT | 8945 |
rs752390473 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101451221 | AATTCGTATAATCAG[G/T]TTGATGTTTTCTTCC | 8945 |
rs752392115 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101467478 | GCTTTGTGTTAAGAC[A/G]CTTCTCCCTCTAGTG | 8945 |
rs752401237 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358836 | GGGTCAAAGCCAGTC[A/G]AGGCCAACTACAGAG | 8945 |
rs752422596 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101414769 | TGGTTTTCAACAAAG[A/G]TGTTTAAATAATATA | 8945 |
rs752429171 | snp | G/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353622 | AACCTGCAGATGCCA[G/T]ATACATGAAATTTGG | 8945 |
rs752465201 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101413399 | GCTCACTGCAGGCTC[C/T]GCCTCCAGGGTTTAC | 8945 |
rs752480166 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383262 | AGAGATAGGGTTTTG[C/T]CCATGCTGAGTTTGC | 8945 |
rs752496634 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101513736 | ATGGAAGCAAAAAAC[-/AT]ATTAAAGTACCAGTC | 8945 |
rs752516841 | in-del | -/TTAA | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352423 | CCTTTTTCTTTTTGT[-/TTAA]TTAATTACTTTTATT | 8945 |
rs752533270 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381474 | GAAGATCCAGTAAGA[A/G]AGTACACATAAAAGC | 8945 |
rs752538854 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101437553 | AAGGAAGGATTTTAA[A/T]TGTCCTCCCAGAGAT | 8945 |
rs752546433 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424268 | CTTGTTTTAGTTTTA[C/T]CACAACCTTGTGCAA | 8945 |
rs752565531 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101474620 | GTGGTTCTCTTTCAT[A/T]TCTGGGATTTCTGTT | 8945 |
rs752569458 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545525 | TAAATAAGGTTAAAT[A/G]AAGTCATTGGAGTAG | 8945 |
rs752570505 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491323 | GTCACAATTTGTAGT[A/G]TAAGCATGCACTGGC | 8945 |
rs752577117 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460366 | TAGTCATTAATTCAA[C/T]TATATCCTTCCTCCA | 8945 |
rs752582095 | in-del | -/TCTCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101472276 | TTTCTTTTCTTTTCC[-/TCTCT]TCTCTTCTCTTCTCT | 8945 |
rs752582146 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400200 | TGATTTGCAAATAGC[A/G]AAGTAAATACACTGC | 8945 |
rs752611009 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514789 | ATCTTTCTTGAAAGT[C/T]AGTTGGCTGTATGTA | 8945 |
rs752634003 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539097 | ATGAATCCCCCTGGT[C/G]AACCCCTTAGTTCTG | 8945 |
rs752659986 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367684 | GGTATGTAAGCTCAT[C/T]TAAATGGAATCATTC | 8945 |
rs752677967 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101376277 | TTTCAGTGAGCCAAG[-/A]TTATGCCACTGCACT | 8945 |
rs752689459 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536082 | TCTTGAGAACTGACT[G/T]TGCATTTCTATTCTC | 8945 |
rs752701001 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101513791 | TAAGGAGGTAAGTAC[C/T]TAAAGTGGAATTGCT | 8945 |
rs752721059 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460474 | TCTGTCCCTTTCTTT[A/G]TAATATAGCATGCTT | 8945 |
rs752745774 | in-del | -/AAAAAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101508918 | ACTCCATCTTAAAAA[-/AAAAAAA]AAAAAAAAAAAAAAA | 8945 |
rs752760677 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554695 | GTGAACAGCATAAAC[A/G]GCTGGACCTCAGCAA | 8945 |
rs752760800 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101536812 | GTGTATTTACCTCTC[A/C]TTGGTTTAGTGTCCT | 8945 |
rs752765131 | snp | A/T | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521830 | CATAAACTCGTATCT[A/T]AAACCTATGTTGCAG | 8945 |
rs752767332 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353230 | TTTTAACCAAACCCT[A/G]GAGTTTTCTCCTCCT | 8945 |
rs752768275 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475480 | GGGAGGTGCAGGTTA[C/G]AGTGAGCCGAGATTG | 8945 |
rs752778296 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446938 | GAGAAGGATACAAGA[C/T]TGATTTTTTTATGTG | 8945 |
rs752784555 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101446251 | AAACGGAAAAATCCT[A/G]CTAGCCTCTAAGGTA | 8945 |
rs752794038 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101486691 | GGCAGGGTTTAGCTA[A/C]CATTTTTATAAAATG | 8945 |
rs752816853 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101354052 | CTCCTTGGCCCCTCA[G/T]CCTGCGCCTGAGAGG | 8945 |
rs752821381 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368880 | AAAAGTTAGCTGGAT[A/G]TGGTGGCGGGCACCT | 8945 |
rs752833065 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523295 | AAAGAAGGATATCTC[A/G]TAAGCCTTGTTGTGG | 8945 |
rs752846882 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101553114 | GCAAGTAAGAAATAT[C/G]AAAAAAGGGGCTAAT | 8945 |
rs752867150 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101368176 | CTCGCTCCATTAGTT[-/C]CTGCCAGAGTTGGTA | 8945 |
rs752879163 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408051 | AAATATAATTAATAT[A/G]GAATTATGAATTAGA | 8945 |
rs752895842 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101469596 | CCTCTGTAAAAAATT[C/T]ACTCCTAAGATACTT | 8945 |
rs752920561 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500295 | CTGTACGCAATCATA[A/G]CATGATGGTGTTTGT | 8945 |
rs752945181 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101402183 | TATCTGATAAATCTA[A/C]ATTCATATGTGAGGA | 8945 |
rs752978148 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507438 | ATAAAGGCTCTGTGC[C/G]GCTCCGATCCGGGGA | 8945 |
rs752983595 | in-del | -/CTC | 1.70577e-05 | 0.00292037 | intron-variant | BTRC | GRCh38.p7 | 10:101532290 | TTCCCATTCCTTCTT[-/CTC]AGACAATAGAATCTA | 8945 |
rs752997033 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101376144 | CAGTCTGGCCAATGT[A/G]GTGAAACCCCGTCTC | 8945 |
rs752999683 | snp | A/G | 5.06812e-05 | 0.00503369 | intron-variant | BTRC | GRCh38.p7 | 10:101535318 | TTTACCAATAAAAGC[A/G]CCAAATCAACTGCTC | 8945 |
rs753007628 | snp | A/G | 1.77603e-05 | 0.0029799 | intron-variant | BTRC | GRCh38.p7 | 10:101414703 | GACAGTGATATTGAT[A/G]ATCCTTGCTCTCTGT | 8945 |
rs753021164 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485011 | CTAGATGTGCGTGCC[A/G]TTTAAGAAAAATACA | 8945 |
rs753021682 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481399 | TCTGGCTAAATAAGG[-/T]TAAAATTTTAGCATG | 8945 |
rs753030375 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537895 | AAAAGATTTTTGGAA[A/G]AGCTACACTTATCTT | 8945 |
rs753060195 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101524814 | TAATGCATGTCTCCA[C/T]CTGCTTATGCTTACA | 8945 |
rs753072757 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101451801 | TGGGCCAATTAACAT[C/T]GAGATGATGAATGGA | 8945 |
rs753112190 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525853 | ATTATTGACACTCAT[C/T]TTACCCAAGCCTCTG | 8945 |
rs753130936 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101471215 | GAATCAACCTTGCAC[C/T]TTCTATTAAAAAGCA | 8945 |
rs753156078 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555211 | ACAGGTCAGACATTT[A/G]AAAGGCATGGGTTTC | 8945 |
rs753158279 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360928 | CCTCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC | 8945 |
rs753159511 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534862 | TGTCAATGTTGTAGA[C/T]TTTGATGACAAGTAC | 8945 |
rs753165019 | snp | A/C | 1.77539e-05 | 0.00297937 | intron-variant | BTRC | GRCh38.p7 | 10:101414633 | GGAGATGACAGGTCC[A/C]TAGATGTTAATTGCT | 8945 |
rs753213291 | snp | C/T | 1.65655e-05 | 0.00287793 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532330 | ATGTGGAAGACATAG[C/T]TTACAGAGAATTCAC | 8945 |
rs753233283 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532212 | AGAGTAAAGCATTGA[A/G]CCATTGATTGTCATT | 8945 |
rs753276889 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101393120 | ATGCTTCCATAAAAA[-/CT]CAAGAGGACTGGGTT | 8945 |
rs753276999 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403400 | AAGATAAATCCTACT[C/T]AGTCATGGTGTATAT | 8945 |
rs753278230 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101390195 | GTGAAGTCACTCACT[C/T]TCTTTTTTTTCATTT | 8945 |
rs753300825 | in-del | -/TGTATATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101505137 | ATATGTGTATATATA[-/TGTATATG]TGTATATATATATGT | 8945 |
rs753311669 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510488 | GCACTCCAACCTGAG[C/T]GACAGATTGAGACTC | 8945 |
rs753321273 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101550611 | AACCATAGCCTTTCC[A/G]TAGACTCCTTTTGAC | 8945 |
rs753323614 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101359702 | GCTTCTGAGGTTCAA[A/G]TGATTCTCCTTCCTC | 8945 |
rs753357117 | in-del | -/ACTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101377166 | ATGAAATCTTCTGTT[-/ACTG]ACCTCTTCCGTTCAG | 8945 |
rs753373839 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481084 | ATGCCACCACACCCA[G/T]CTAATTTTTGGTTTT | 8945 |
rs753374798 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101466368 | TCTCTTGTGTAGCTG[A/G]AACCCTGGGGATGCA | 8945 |
rs753386539 | snp | C/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515110 | ACAGGCATGCACCAC[C/G]ACACCCGGCAAATTT | 8945 |
rs753389603 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369820 | TAATTGTAACTCCAT[A/T]TTCTGACAGTGAGTA | 8945 |
rs753395594 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425458 | TGAAGAAACTAATAT[A/G]TGCTGTGCAGGGCTG | 8945 |
rs753437125 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410306 | ATTTTCATTTTCCCA[A/G]TGACCGCTGATGTCA | 8945 |
rs753437917 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356262 | CCTTGGCCTCCCAAA[C/G]TGCTGGGATTTCAGG | 8945 |
rs753455728 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411656 | TTTTATACCCTACAT[C/T]ACTATGTTCATGTTA | 8945 |
rs753478966 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101464060 | ATCTAAACCAATAGG[A/G]CAATACTGAATAAGA | 8945 |
rs753488135 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502169 | CCTGGCTCTTGTCTT[G/T]GCTGATTCTAAAACA | 8945 |
rs753494190 | in-del | -/TTTTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101388336 | CCCAGCTAATTTTTA[-/TTTTA]TTTTATTTTATTTTA | 8945 |
rs753520814 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519821 | ACCAACATGGAGAAA[C/T]CCCGTCTTTACTAAA | 8945 |
rs753522186 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465364 | TTGCCATTGTTGATA[A/G]GACATAACTACTGCA | 8945 |
rs753531962 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101451971 | CAAAATATATACACA[C/T]TGGAGTTGTCACGAG | 8945 |
rs753536533 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101513269 | TATCAGTAGGAATAC[C/T]GTACTCTTAGAAGTT | 8945 |
rs753537434 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482586 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGCGTT | 8945 |
rs753568040 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439380 | TACGTTGATCCGATG[A/G]TGTCCTGACCTCTAT | 8945 |
rs753570822 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543377 | GTGGTGTATCTTACT[A/G]TATTCTTTTACTTTT | 8945 |
rs753577635 | snp | A/G | 1.65176e-05 | 0.00287376 | intron-variant | BTRC | GRCh38.p7 | 10:101532932 | CACATTGATCAAAAG[A/G]ATCTTATTTGCCATC | 8945 |
rs753591334 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101416128 | CTTTTTGTGACTGGC[-/T]TTATTTCACTCAGCA | 8945 |
rs753591564 | in-del | -/GTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101389116 | TGTGATTTTTTGTGT[-/GTG]GTGTTTTTTTTTTTT | 8945 |
rs753635445 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488725 | GAATTCAAATATCTT[C/G]TAAAGATACACAAAA | 8945 |
rs753639521 | in-del | -/TATATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101404003 | GTATGTGTGTGTGTG[-/TATATA]TATATATATATATAT | 8945 |
rs753651815 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474435 | GTCAAACTCTAAACT[C/G]TTTCTCCCCCCATGA | 8945 |
rs753652305 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504122 | CAGCATCACAGAAAT[G/T]TTATTCTGGTAATCT | 8945 |
rs753720284 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550776 | TGATGACACAATCCT[C/T]ATCTGGGACTTCCTA | 8945 |
rs753738446 | snp | A/G | 1.65542e-05 | 0.00287695 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532383 | GAGTTTACTGTTTAC[A/G]GTATGATGATCAGAA | 8945 |
rs753755830 | in-del | -/AG | | | intron-variant | BTRC | GRCh38.p7 | 10:101489390 | ATTCCTTAATCTGAA[-/AG]AGAGATTTTTATTCT | 8945 |
rs753757386 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101531472 | GCTGGCCATGGTGGC[G/T]CACACCTGTAATCCC | 8945 |
rs753778467 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101385366 | ACGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8945 |
rs753784349 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458026 | TTGAAAGTTACAGAC[A/G]TAATGTTCCATCCCC | 8945 |
rs753806268 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420270 | GATCTGCCACCTTTA[C/T]TTGATCAATCTTCCT | 8945 |
rs753874564 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487595 | GAACAATCAGTTTAC[A/G]CAGATAGCTCCTGAT | 8945 |
rs753880469 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503523 | GATAAATTAAGAAAA[C/G]AATTACCAAAGTATT | 8945 |
rs753935532 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459183 | ATTGGATATAATTTA[A/G]CCTGATGATCTAGGA | 8945 |
rs753947085 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499165 | AAGCTTAAAGAAGGC[A/G]ACTAACTTGTTCAGG | 8945 |
rs753951074 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101367575 | CTTTGCCAGCACTCC[A/G]CAAGTTGCCTTCATG | 8945 |
rs754015236 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514743 | CAGGCATGAGCCACC[A/G]TGCCTGGCCTCCCCA | 8945 |
rs754031939 | snp | C/T | 1.69232e-05 | 0.00290883 | intron-variant | BTRC | GRCh38.p7 | 10:101535305 | ATTTGCCATAGATTT[C/T]ACCAATAAAAGCACC | 8945 |
rs754035112 | in-del | -/TTTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101520139 | TTTGCTTGTATTTTG[-/TTTG]TTTGTTTGTTTGTTT | 8945 |
rs754036175 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423148 | TGAACTCCTGGTCTC[A/G]AGCAGTCCTCCCACC | 8945 |
rs754064035 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401171 | CAGAATAGCCAAGTA[A/G]TTTTGTTGTGGCATG | 8945 |
rs754097843 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460257 | TAAACATACAACTTG[A/G]TGTTATGGGGTAAAT | 8945 |
rs754113516 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101549267 | AGACCTAATCTCTAC[-/A]AAAAAAAAAAAAAAA | 8945 |
rs754151112 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101521183 | GGAGGCTAAGGTGGG[A/C]GGATCGCTTGAGCCC | 8945 |
rs754171011 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101553081 | TTGGCAGCTAAGTGA[A/G]TGTTCTTTTGTCTTC | 8945 |
rs754180144 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101537711 | TGTAGACTGCTCACT[A/T]CTTCTGCTTTGGGAC | 8945 |
rs754185814 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101478384 | TCTTTTCTTTTTAAA[-/G]CCAAAAGTCAAAGCT | 8945 |
rs754190275 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101375818 | CCTTTTACTTGGTAC[A/G]CCTAAAAAATTGGCA | 8945 |
rs754206593 | snp | A/G | 7.10189e-05 | 0.00595856 | intron-variant | BTRC | GRCh38.p7 | 10:101414621 | ATTGATGTCATAGGA[A/G]ATGACAGGTCCATAG | 8945 |
rs754209642 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511851 | AGACGAAGTTTCACT[A/G]TGTTGACCAGGCTGG | 8945 |
rs754250101 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101419723 | CAAGCGGTGGGAAAC[A/C]TCGGGGGGCATGTTA | 8945 |
rs754250623 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101552630 | TTAATCTCCAGGCCA[C/T]ATTTCCAGCTGCCAT | 8945 |
rs754257863 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101368527 | CTCTGTTGCCCAGGC[C/T]GGAGTGCAGTGGCAT | 8945 |
rs754280354 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553578 | ATGGGGGATGCAGCT[C/T]CAAGCCCAGTGCCCA | 8945 |
rs754294353 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362047 | CTCACTGCAACCCCC[A/G]ACTCCCTGGTTCAAA | 8945 |
rs754326451 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101368510 | TAGAGACAGGGTCTC[-/A]ACTCTGTTGCCCAGG | 8945 |
rs754364195 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101453997 | AACTTTATTTGCAAA[A/C]ATATGTGTCAGGCCA | 8945 |
rs754367468 | in-del | -/TT | 1.65567e-05 | 0.00287716 | frameshift-variant, intron-variant | BTRC | GRCh38.p7 | 10:101531291 | TGCTCCTCCCAACTC[-/TT]TTTATAGAGCACTTT | 8945 |
rs754370481 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523063 | ACAAAAATTAGCTGG[A/G]TGTAGTAGCACACAC | 8945 |
rs754408050 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521959 | CTCTTTAAAAGTCTT[C/T]ATTGGCTTGATTTTT | 8945 |
rs754432449 | in-del | -/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101527762 | CTGTCTCTTTCTCTG[-/TC]TCTCTCTCTCTCTCT | 8945 |
rs754445185 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469423 | TCCCTCAGGCCTGGC[A/G]CAGAGTTTCTGAATC | 8945 |
rs754468265 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101464192 | AATTTTCTCTCTGCA[A/G]AGTTATAAATTAATT | 8945 |
rs754478528 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556580 | ACCAACAGACCAGAC[C/G]TCCTTTAACCACAGT | 8945 |
rs754484999 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407262 | CTGAGGCAGGAGGAT[C/T]TCTTGAGCTCAGGAG | 8945 |
rs754500291 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371907 | AGGCACACCTCACAC[A/T]TGAGGCTGAAAACCC | 8945 |
rs754536718 | snp | C/T | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557557 | CATTGGTCACCTTAG[C/T]CAACCACAGCCCAAC | 8945 |
rs754542543 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101451185 | GTAATCAGGTAGCAG[C/T]ATTAAAAGAACAGAA | 8945 |
rs754543749 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427263 | GCTGGGACTATAGGC[A/G]TGCACCACCATACCC | 8945 |
rs754545076 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516825 | TTCATTAAGCTGCTG[A/G]TTGTTCTTCTCTGTT | 8945 |
rs754564368 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377353 | ATAAAGCTGCTATAA[A/G]TAAACACTTGTGTAT | 8945 |
rs754574888 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101541659 | CATGTTGGATTTTGT[A/G]AAATGCTTTATCTAC | 8945 |
rs754582608 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436846 | AATGCTTACAAGTCT[A/G]CTGAATTTTACCATG | 8945 |
rs754600422 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101466523 | CCTCTATAGATGGAG[A/G]CTTCACCTGCAGTGA | 8945 |
rs754607414 | snp | C/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515147 | TTTTAGTAGAGACAG[C/G]GTTTTACCCTGTCAG | 8945 |
rs754627738 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465559 | CATCAGAAGGGACAT[A/G]TGGTTTTACTGGTGA | 8945 |
rs754630807 | snp | C/T | 1.70246e-05 | 0.00291754 | intron-variant | BTRC | GRCh38.p7 | 10:101430312 | CCATCCTGTCTCATA[C/T]TGTCCCATCTCATAG | 8945 |
rs754632984 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434790 | ACATGGCTGAAACCC[C/T]GTCTCTACTAAAAAC | 8945 |
rs754657510 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357372 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 8945 |
rs754681555 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363899 | CTGTTGTCACAGTAT[C/T]ATTTCAGTTAGCTAT | 8945 |
rs754682336 | snp | C/G | 4.98235e-05 | 0.00499092 | intron-variant | BTRC | GRCh38.p7 | 10:101430464 | CCAGGTACTTTCTCT[C/G]TCTCTGTGGGTTATT | 8945 |
rs754701947 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550785 | AATCCTCATCTGGGA[C/G]TTCCTAAATGATCCA | 8945 |
rs754706537 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502325 | ATAATTTCCTTACTG[C/T]TCTTCCTTCCCTGAA | 8945 |
rs754709053 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101411725 | GTCAGTTTTTTTCTG[A/G]GTCTGCTTCCATTGA | 8945 |
rs754750779 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526897 | TTCTGACTTAATTCC[A/G]AATTCCCCAAAGCAT | 8945 |
rs754770977 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543585 | ATTTTCCATTTTTTG[C/T]TTTTGTTTGTTACCT | 8945 |
rs754773821 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488797 | TACTAATATGCAAAA[A/G]CTGGTTACCAGGTAC | 8945 |
rs754779091 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101398678 | GTTGCGTACACTAAT[A/G]CCATCATCCTTTGCC | 8945 |
rs754797222 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490017 | TTGGCACTTACCCAA[C/T]ACACCCTTAATTAAA | 8945 |
rs754867077 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459213 | AAAATTATGCACATA[C/G]CTTATTGGGAATCCT | 8945 |
rs754872515 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485684 | CGGTTCAGCTGTTGG[G/T]AACCACTGATATATC | 8945 |
rs754873116 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101528125 | CTGAAATTTCAGTTA[A/C]GGAGATTCATTCCTT | 8945 |
rs754874015 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458059 | TAAATGTTTCAGTGC[A/G]TGTTTCCAGAAAAAC | 8945 |
rs754962014 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352243 | GTGTAGAATTTTTTT[A/G]AAAATTCAAGAACAA | 8945 |
rs755004682 | snp | A/G | 3.30213e-05 | 0.00406319 | intron-variant | BTRC | GRCh38.p7 | 10:101538421 | CAGGTGGGGGAAGAA[A/G]TTAAACGTTGATGTG | 8945 |
rs755025320 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460328 | TAGCATGTATTGCCA[A/G]TCGCCTCATTTGTCA | 8945 |
rs755026367 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420304 | TAATCCATCTCCTGT[C/T]GCTGACATATCTCTC | 8945 |
rs755030171 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101513615 | TGTCTGTGGTTTATT[A/C]TTTTTGTTGCTGAGT | 8945 |
rs755113227 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503551 | ATTCCAGAGAGAAAT[A/G]TCTTCAGTCCCTTGA | 8945 |
rs755116936 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101391476 | TTGTTACAACAAATA[C/T]CAAATGGAAAAATTG | 8945 |
rs755128932 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406985 | CCTTCTTTGTTTATA[C/T]TTGCACTGTCCAATA | 8945 |
rs755172427 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431191 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 8945 |
rs755177621 | in-del | -/C | 1.67705e-05 | 0.00289568 | intron-variant | BTRC | GRCh38.p7 | 10:101531361 | TATTTTGGGGTATTG[-/C]CCCAAGGGCACAGAA | 8945 |
rs755194161 | snp | A/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534721 | CCATTGTGAAGCAGT[A/T]CTGCACTTGCGTTTC | 8945 |
rs755226162 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101429339 | AATAATACTAATGTC[A/C]GTTACTTAGAGCTAC | 8945 |
rs755239433 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442012 | GATTTGAATGATGGA[A/G]AAATTTCTAGGAACT | 8945 |
rs755247793 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499193 | AGGTCTATATAGCTT[C/G]TACATGGCAGACACT | 8945 |
rs755264540 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101445962 | TCATGGAGAATACTG[A/C]ATAGGAATGATAATG | 8945 |
rs755279010 | snp | A/G | 1.77539e-05 | 0.00297937 | intron-variant | BTRC | GRCh38.p7 | 10:101414622 | TTGATGTCATAGGAG[A/G]TGACAGGTCCATAGA | 8945 |
rs755287816 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101523076 | GGGTGTAGTAGCACA[C/T]ACCTGTTATCTCAGC | 8945 |
rs755297141 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360661 | TAGGCATTAGCTACC[A/G]CGTCTGGCCTCTAGA | 8945 |
rs755320792 | snp | A/C | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534839 | GTGCTGGTCGGACAC[A/C]GAGCTGCTGTCAATG | 8945 |
rs755352614 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359097 | CCTGCGTGACTTCCC[A/T]TAATGATGTCACTGT | 8945 |
rs755387661 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101547065 | ATATAGGAAAAGAAA[A/C]ATACAGACTAATAAT | 8945 |
rs755392038 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439040 | GCTCTCCCTAGGTTT[A/G]TGAATGTAGTTAGAT | 8945 |
rs755428307 | snp | C/T | 3.3e-05 | 0.00406189 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526180 | TCTCTGTGGAGAGGC[C/T]TGGCAGAACGAAGAG | 8945 |
rs755449854 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101552739 | GCTGGTACCCTGCAG[C/G]CACACAGCCAGGCCA | 8945 |
rs755460550 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101455880 | GGCATGGTGGCTTAC[A/G]CCTGTAATCCCAGGA | 8945 |
rs755477503 | snp | A/G | 1.65556e-05 | 0.00287707 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531286 | GGGAATGCTCCTCCC[A/G]ACTCTTTTTATAGAG | 8945 |
rs755481178 | in-del | -/AAAAAAAAAAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101549713 | GCGAGACTCTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 8945 |
rs755505539 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507301 | AAACATAAACACAGC[A/G]CTCATTTCTGGCAGG | 8945 |
rs755526997 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493421 | AGATTAAGTAATTTG[C/T]CCAAGGTCATACTGT | 8945 |
rs755528407 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101383927 | TATGTTGCCCAGGCT[A/G]GACTCAAACTCCTGG | 8945 |
rs755535382 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101540154 | TGACTTTTTCTATTA[C/T]GGCCTATGTTACTTG | 8945 |
rs755536624 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402053 | TTTTATAGGAAGTTA[C/T]GAAAAAAAGTCTATA | 8945 |
rs755571356 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385283 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGT | 8945 |
rs755592100 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101400668 | CTCTGATCTTTCCTA[C/T]GACGGCCAGCCTGGC | 8945 |
rs755601448 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434142 | CTCATGTCTGCTTCT[G/T]CACTCAATCTATTGT | 8945 |
rs755617852 | in-del | -/TGTGTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101403990 | TCCTATCTATGTGTA[-/TGTGTG]TGTGTGTGTGTGTAT | 8945 |
rs755630732 | snp | A/G | 1.78204e-05 | 0.00298494 | intron-variant | BTRC | GRCh38.p7 | 10:101414731 | TGTGGGCCTAGGCTA[A/G]TGTAATGTGTGTGTT | 8945 |
rs755670258 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515257 | CACCACACCTAACCG[G/T]TTTTTTTATTTTCAG | 8945 |
rs755684478 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358219 | TGATCCTCCTGCCTC[A/G]GCGTCTCAAGTGGCT | 8945 |
rs755689728 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101442889 | AGATCTCACTTGCTC[-/T]TTTTTTTTTTTTTTT | 8945 |
rs755690664 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386269 | TGCCCAGCAAGGTCA[A/G]TTTACTCTAGTAAGT | 8945 |
rs755696736 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509763 | GATGGAGTCTCACTA[C/T]GCTGCCAAAGCTGGT | 8945 |
rs755703526 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555095 | TTCTACTTGGCCACT[A/G]TCAGGGTTCGTCATC | 8945 |
rs755735107 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101480450 | CCAAGATGAGAGCAC[C/T]AGCAGATTCAGTGTC | 8945 |
rs755764938 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436203 | TGGAATCATTTGCTC[A/G]TTCCCAGCAAATGGT | 8945 |
rs755765622 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101542467 | GTCTTCTGTATCCTT[A/G]GTGATTTTTCTATTC | 8945 |
rs755770833 | snp | C/T | 6.5925e-05 | 0.00574092 | intron-variant | BTRC | GRCh38.p7 | 10:101538398 | GCTGTTTAGAGAGCA[C/T]TGGAGAGCAGGTGGG | 8945 |
rs755774420 | snp | C/T | 3.35632e-05 | 0.0040964 | intron-variant | BTRC | GRCh38.p7 | 10:101531362 | TATTTTGGGGTATTG[C/T]CCAAGGGCACAGAAT | 8945 |
rs755860156 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101411450 | TGTGTTAGACCACTT[-/A]ACAATTTCCTATAGG | 8945 |
rs755899784 | snp | A/G | 0.000148604 | 0.00861859 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532353 | GAATTCACTGCCGAA[A/G]TGAAACAAGCAAAGG | 8945 |
rs755902428 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101488412 | ATCAAGTAAGGTGTT[-/TA]TAGGAGGAAGAAGGA | 8945 |
rs755928353 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482685 | CAGTCGTGAGCTGCC[A/G]CATCCGGCCAACTGT | 8945 |
rs755937596 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502006 | AAATCTGCAATCTCT[G/T]GTCTATGAAACCCCA | 8945 |
rs755991862 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517208 | ACATCCACCTCAACA[C/T]ACCAGGATTACAGGT | 8945 |
rs755998630 | snp | A/G | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479419 | GAAACAGTATGTTTA[A/G]CAAGCACTGCTATGA | 8945 |
rs756006292 | snp | C/T | 4.94425e-05 | 0.0049718 | intron-variant | BTRC | GRCh38.p7 | 10:101538262 | TACATTTGCTTTTAA[C/T]TAACATTTTTGTCCC | 8945 |
rs756006786 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101473084 | TTGGACTCCAGCCAC[A/G]CATATATTCTAGATA | 8945 |
rs756016294 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101479815 | CATCACATCATTGCA[A/G]GGACTGTGAAATATG | 8945 |
rs756025537 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419159 | GGAATTATAGGCACA[C/T]ACCACCATGCCTGGC | 8945 |
rs756037931 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525572 | AAGGACATTTCTTTT[A/G]CCGAACAGCTTTGGA | 8945 |
rs756051564 | snp | A/C | 2.53213e-05 | 0.00355809 | intron-variant | BTRC | GRCh38.p7 | 10:101521627 | TATGTTTCTTTTAAC[A/C]CCCTTCTACAGACAA | 8945 |
rs756060040 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101471704 | ACAAACCACTTGGGC[C/T]TGTAGTTTTCTTTGT | 8945 |
rs756061370 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435587 | ACAATTTGTTTATCC[A/G]TTCATTTATTGATAG | 8945 |
rs756074420 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380109 | TAGATTGGTAGGTAA[A/G]TTTTACGTTGTACCA | 8945 |
rs756117836 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101396889 | CTCACCGGAACCTCC[A/G]CCTCCCGGATTCAAG | 8945 |
rs756120738 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534689 | AATACAGGTGAAATG[C/T]TAAACACGTTGATTC | 8945 |
rs756127785 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452798 | CTTGATGTGGTTGTG[A/G]TTTAATAGAGTATGT | 8945 |
rs756157541 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101526623 | CAACTCTACTAAAAA[C/T]ACAAAATTTAGCCGA | 8945 |
rs756165839 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101458285 | TACGTACGATATAAT[G/T]CCATTTATATGACAT | 8945 |
rs756172152 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101474300 | TTGTATTTGTTAAGG[C/T]CAGGTGTATTTTGGT | 8945 |
rs756174497 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465816 | CCAGCATCTGAAGAT[-/G]GAAGAGTTTGGGGTA | 8945 |
rs756177557 | in-del | -/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101531341 | ACATTGAGGTAAGAA[-/TC]TATGTATTTTGGGGT | 8945 |
rs756179798 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101420108 | CCTAGGAATTTCTCG[C/G]TGTAATACATTGTAA | 8945 |
rs756183390 | in-del | -/GGTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101511548 | GTATTTTGGGTTTTT[-/GGTTT]TGTTTTGTTTTGTTT | 8945 |
rs756208347 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101424422 | ATTATGGTATACTGC[A/C]TTTCTCTGAATTTCT | 8945 |
rs756230948 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101397604 | AATGATTTTTTTGGT[A/G]GCAAATTTAGAAAGC | 8945 |
rs756243697 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101529478 | GAATGTGGGTGGGCT[C/T]AGGAGTCAGACTTAA | 8945 |
rs756270017 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101462681 | CAAAACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 8945 |
rs756274757 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363785 | ATATCTCTCTGAGGT[A/G]GGCAGTCAAGCGGTG | 8945 |
rs756294012 | snp | C/T | 3.34638e-05 | 0.00409033 | intron-variant | BTRC | GRCh38.p7 | 10:101550896 | TACTTGCCCAGGTAT[C/T]GAAATCGATTATGTA | 8945 |
rs756296172 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101443490 | TATAGAATGTGTATG[A/T]GTGCATACAAAACCA | 8945 |
rs756312070 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445048 | TTTCTGGTAGAAACT[C/T]GATATGTTAGGGTTT | 8945 |
rs756321952 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510945 | CCTTCTAATTGATCT[G/T]TCTTCCTCTGCTTTT | 8945 |
rs756333674 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459152 | TATATTAATCACTTA[C/T]CCTTAAATAGAATTT | 8945 |
rs756348256 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101503179 | GATATTCTATTACAT[-/A]AACTCCTTCAGAAAG | 8945 |
rs756373694 | in-del | -/CAGTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101376725 | GAAAAGGATGTAATT[-/CAGTA]CAATTAAATAAGGTA | 8945 |
rs756421008 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536434 | CTGTGTGGGTGGTGA[C/T]TGATTTTATTTTATG | 8945 |
rs756450284 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526144 | TGGAAGAAGCTTATC[A/G]AGAGAATGGTCAGGA | 8945 |
rs756474535 | snp | C/T | 1.77928e-05 | 0.00298263 | intron-variant | BTRC | GRCh38.p7 | 10:101535513 | AAGGGATCAATATTA[C/T]GCTCCCATTCATTAT | 8945 |
rs756485058 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392550 | TGCCCAGGCTAGAGT[A/G]CAGTGGCGGCATGGT | 8945 |
rs756488092 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465798 | TGCTTTTTCGTTTCA[C/T]TTCCAGCATCTGAAG | 8945 |
rs756503813 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101549393 | CTATGATCACACTAC[C/T]GCATTCTAGCCTAGG | 8945 |
rs756505095 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471566 | GTTTGCCAGGTTTTG[A/G]TATCAGAGTTATGCT | 8945 |
rs756527898 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101526224 | TAACTTTTCTTACTC[C/T]TATACGGCTTCAGGA | 8945 |
rs756536608 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483755 | AGCATGATGAGCTCT[A/G]TGTTTATTGTAGCTT | 8945 |
rs756558900 | in-del | -/AATCAATACTTAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101546860 | CCCAGATCTTCACAG[-/AATCAATACTTAAT]AATTATCTTTCCAAA | 8945 |
rs756560399 | snp | A/T | 0.000244477 | 0.0110535 | intron-variant | BTRC | GRCh38.p7 | 10:101535498 | AGTGCCTTGTATCAT[A/T]AGGGATCAATATTAT | 8945 |
rs756573674 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101527788 | TCTCTCTCTCTCTCT[-/A]CTCACATACACACAC | 8945 |
rs756590611 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101544824 | AGCACTTTGGGAGTC[-/TG]AGGCGGTGGATTGCT | 8945 |
rs756591639 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498305 | ACCACAGACATGTGC[C/G]ACCACGCACAGCTAA | 8945 |
rs756637963 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101430781 | AATATTTGCTCTGGA[C/G]CTACATAAAGCCAAT | 8945 |
rs756647532 | snp | C/G | 3.46614e-05 | 0.00416287 | intron-variant | BTRC | GRCh38.p7 | 10:101526002 | TCTTTGCCTCCTCCC[C/G]CTACTGAAAGCTCGG | 8945 |
rs756678710 | in-del | -/AAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101445317 | CACATGCATACAGGT[-/AAG]AAGATTAGAAAAAAA | 8945 |
rs756684400 | in-del | -/TATT | | | intron-variant | BTRC | GRCh38.p7 | 10:101383876 | ATAGGGTATTTTATC[-/TATT]TATTTATTTATTTTT | 8945 |
rs756720660 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101414028 | TTTAAGTGTACAATT[C/G]AGTAGTTTTAGCACA | 8945 |
rs756766939 | snp | A/G | 1.66098e-05 | 0.00288177 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531323 | ATCCTAAAATTATAC[A/G]AGACATTGAGGTAAG | 8945 |
rs756802578 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536623 | GTATTCGATTTGATA[A/G]CAAGAGGATAGTCAG | 8945 |
rs756804108 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546865 | ATCTTCACAGAATCA[A/G]TACTTAATAATTATC | 8945 |
rs756853264 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101400555 | CTAAGGATTTGCCTC[C/T]TCTCCCTATCAATGA | 8945 |
rs756867414 | in-del | -/GTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101357826 | TTACTTGTGAAAAAA[-/GTT]TAAGCAGAATGTTTA | 8945 |
rs756878195 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493297 | TTTGACAGCCTTTTT[A/G]CACCATTACAGGTAT | 8945 |
rs756896759 | in-del | -/ATGGTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101463246 | AACGGGGTTTCACCA[-/ATGGTG]TGTTGGCCAGGCTGG | 8945 |
rs756908949 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355158 | GGCCAGGTGCTTTGT[A/G]TCATTTTCTGGGAAA | 8945 |
rs756911446 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460617 | GGCTTACTAAAGGTG[A/G]CACACAGGTGTCAGC | 8945 |
rs756928707 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368126 | TGCGTTCCTCATGAA[C/G]GGCTTGGTGCCATCC | 8945 |
rs756958877 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423713 | AAGAAGGTAATGCTT[A/G]AATGAAATAATGTAC | 8945 |
rs756984165 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476491 | TTTCTTTTTTTAAAG[A/T]GATGATGTCTTGATT | 8945 |
rs757001818 | snp | G/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354179 | CAGTGGCCTCGGCGA[G/T]TATGGACCCGGCCGA | 8945 |
rs757015335 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515054 | TCCACCTCCCGGGTT[C/T]AAGCAATGCTCCTGC | 8945 |
rs757015450 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368934 | TGACGCACGAGAATC[A/G]CTTGAACCTGGGAGG | 8945 |
rs757028314 | snp | A/C | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479409 | CTTAAACCAAGAAAC[A/C]GTATGTTTAGCAAGC | 8945 |
rs757033314 | snp | A/T | 1.66527e-05 | 0.00288549 | intron-variant | BTRC | GRCh38.p7 | 10:101536699 | AAAATCTACGTCTTA[A/T]TCCTTCCTTATGTTT | 8945 |
rs757040408 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424478 | ATTCTTCTATTCCAT[-/G]GCTTAAGGATACGTA | 8945 |
rs757045528 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101508088 | AAATGTTAAATGACT[A/G]TCCTGTCCCTTTAAC | 8945 |
rs757046868 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402637 | TTGTGGAATTTTATT[G/T]CTGTAAGGTAGTTAG | 8945 |
rs757049326 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555021 | ATACATCGTAGCCTA[A/G]GAAATATTTTCTCAA | 8945 |
rs757076643 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372443 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 8945 |
rs757079848 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101374791 | GTATAATAAATAAAA[-/A]AAAAAAAAAGAAAAG | 8945 |
rs757105825 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433915 | CTTTTGTTTATATGG[C/T]TTATATCTATTGATA | 8945 |
rs757131501 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101539830 | TACTCCACATTCTTG[-/C]CAGTACTGAGCACAG | 8945 |
rs757134607 | snp | A/T | 1.65296e-05 | 0.00287481 | intron-variant | BTRC | GRCh38.p7 | 10:101533091 | AAATTTCAAATGCTT[A/T]TTTGAACTCTGAAAT | 8945 |
rs757158110 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433091 | AAGTTCCAGGGGCCC[A/G]GAGACCGCTTTCCAG | 8945 |
rs757177690 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505946 | TTGAGACGGAGTCTC[G/T]CTGTGTCGCCCAGGC | 8945 |
rs757187514 | snp | A/C/T | 5.21529e-05 | 0.00510629 | intron-variant | BTRC | GRCh38.p7 | 10:101462095 | AAAATAAAAAGCTAC[A/C/T]AACAGCAAAACAAAA | 8945 |
rs757187755 | snp | A/G | 6.59772e-05 | 0.00574319 | intron-variant | BTRC | GRCh38.p7 | 10:101534650 | ATCTAAATCTCATCT[A/G]TCACTTCCAGAGTGT | 8945 |
rs757202582 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449310 | GGAAACAAGGATGAC[A/G]GAAAAAAAAAATTCA | 8945 |
rs757209949 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485402 | AGCCTGAAGTCCAGC[C/T]GCATTGATTAGGCAC | 8945 |
rs757217253 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394584 | GTCACAGACTGACTA[A/G]TAATGAGTAAAACAA | 8945 |
rs757243583 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101369159 | TGACTGTTTAGACAT[A/C]GTCTTTTGTTGAAGT | 8945 |
rs757252274 | snp | A/C | 1.65083e-05 | 0.00287296 | stop-gained, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550848 | TCGAACATACACCTA[A/C]ATCTCCAGATAAATA | 8945 |
rs757272430 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101409872 | ATAATGCTACTATGA[A/G]CATGTGTATACATGT | 8945 |
rs757308327 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421292 | CATTCCTGTGCCCCT[A/G]AACCATTTTGGCTTC | 8945 |
rs757337994 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101452118 | TTTGATTATTTGCTA[A/C]TGTCTCAAGAGGGAG | 8945 |
rs757346376 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555774 | AAACAGAGCTGAAGG[C/T]GTCCCCATTGTAGAT | 8945 |
rs757356574 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417511 | GTGAATTTCTTCCAA[A/T]ATTAGTGATATTAAT | 8945 |
rs757368920 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487068 | ATAGAAATAATTTTG[A/G]TTCCTAAGTAATAAA | 8945 |
rs757396822 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101529046 | AAAAGACCACTTGGG[-/A]AAAGTCAATTTTCTT | 8945 |
rs757411123 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101507847 | ATGTCCTTTTTTTTT[C/T]CCTCACCACTAGGAC | 8945 |
rs757414522 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101378128 | GAAGTAATTTAGATG[C/G]AGGCAAGGAAGGCTT | 8945 |
rs757418300 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101523488 | GAGAAAAAAATCATA[C/T]CAGCATGAATGAATC | 8945 |
rs757427306 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101456479 | TGGGAGGAAAAGAGC[C/T]GACCTAGAAATGAGT | 8945 |
rs757456144 | snp | G/T | 1.87383e-05 | 0.00306085 | intron-variant | BTRC | GRCh38.p7 | 10:101525986 | CCTTCTGTGTTCTTT[G/T]TCTTTGCCTCCTCCC | 8945 |
rs757502415 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441100 | TCAAAAATCATTCTT[A/G]TAGAAATTGATTTCT | 8945 |
rs757507342 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472870 | TTTTTCCTTGGCTCC[A/G]TTCAAGGTTTTATCT | 8945 |
rs757516910 | in-del | -/AAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101545574 | TGGTGTCCTTAAAAC[-/AAG]AGGAGATTGGGACAC | 8945 |
rs757521350 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363715 | AAGAGCTCTTTAGCA[A/G]CTTTGTAGAAGAAAG | 8945 |
rs757534704 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424276 | AGTTTTACCACAACC[G/T]TGTGCAATAAGGCTG | 8945 |
rs757557012 | snp | C/T | 0.000164766 | 0.00907502 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550816 | GCTGCCCAAGCTGAA[C/T]CCCCCCGTTCCCCTT | 8945 |
rs757584634 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510657 | TTGTTTCTCCTGGCC[A/G]CAGGAGCAAGAACAC | 8945 |
rs757612458 | snp | A/G | 1.70113e-05 | 0.00291639 | intron-variant | BTRC | GRCh38.p7 | 10:101535476 | CAACACTATCAGGTG[A/G]GCAGCAAGTGCCTTG | 8945 |
rs757628733 | in-del | -/TTTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101520136 | AGTATTTGCTTGTAT[-/TTTG]TTTGTTTGTTTGTTT | 8945 |
rs757634189 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411972 | GCTTTTATTCTAGTG[C/T]AGTTCATCCCAGCAA | 8945 |
rs757645385 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404721 | AGTCTATGCCTGGCC[A/G]AGTGCAGTGGCTCAC | 8945 |
rs757655476 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543976 | TGCACTGGCGTGATC[-/T]TTGGCTCACTGCAAC | 8945 |
rs757662448 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443242 | TTGGGCAAGTTTTAA[A/G]CCCTCCTAAGTGAAG | 8945 |
rs757667034 | snp | C/T | 1.65067e-05 | 0.00287282 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430436 | ACCCAGGGACTGGCG[C/T]ACTCACAGCTTTCCA | 8945 |
rs757690146 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101495385 | GCAAAACTGGCATAG[A/G]CAGCCTATTAATTAT | 8945 |
rs757695743 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101371995 | ATAGCCAGCTTATTC[A/C]GCACTATTTATTGAA | 8945 |
rs757719903 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482705 | CGGCCAACTGTTTCT[A/G]TTGGCCTCTATTGCT | 8945 |
rs757722992 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101534996 | AATTTCATATTTAAA[C/T]GTTGCTACAGAAAAA | 8945 |
rs757725330 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465693 | AGTAATTCCAAAACC[C/T]GACAAAGATATTACC | 8945 |
rs757745628 | in-del | -/AG | | | intron-variant | BTRC | GRCh38.p7 | 10:101526338 | AGCTTAAAATGTAAC[-/AG]AGAACAAATGTTCAT | 8945 |
rs757755252 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546666 | AATTCAAAGTAAGTA[A/G]AAGAAAAGAAATAAC | 8945 |
rs757763743 | in-del | -/TAGTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101489990 | TGGAGAAATTTTCAT[-/TAGTC]TAGTCCTTTGGCACT | 8945 |
rs757770475 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428684 | GGATAAATACTTAAT[G/T]TTTCCTGGGCATCAG | 8945 |
rs757806928 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101391094 | TTCTTGATATGGAAT[A/G]CAATCTGATTTGTCT | 8945 |
rs757808949 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362343 | TGCCTTCCTGCTCCT[A/G]GGCTTGTGACCTGAC | 8945 |
rs757828778 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370506 | GCCCTGACAAAATGA[A/G]TAGAGGTTTATTGTA | 8945 |
rs757859051 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101357615 | ACAACTTTTATACAG[A/G]TGTCATGATTTCCAT | 8945 |
rs757892246 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536575 | GTGGTGCATGTTTAC[A/G]AGTGTTAGAAGGCCA | 8945 |
rs757894488 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543843 | CTACAGATTTTACTT[C/T]TAAATATGTTATCAT | 8945 |
rs757908721 | in-del | -/TTAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101498019 | GCGAGACTCCGTCTC[-/TTAA]TTAATTAATTAATTA | 8945 |
rs757942971 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101545577 | TGTCCTTAAAACAAG[A/T]GGAGATTGGGACACA | 8945 |
rs757945127 | snp | C/T | 3.30841e-05 | 0.00406706 | intron-variant | BTRC | GRCh38.p7 | 10:101462072 | AGGTATGAAATTCAG[C/T]CTTACTTAAAATAAA | 8945 |
rs757945591 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101413429 | CACCATTCTCCTGGC[C/T]CAGCCTCCCGAGTAG | 8945 |
rs758000116 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456201 | GATGATTGCCACTCT[A/G]GTGTATAGAATATAT | 8945 |
rs758045218 | snp | C/T | 1.80302e-05 | 0.00300246 | intron-variant | BTRC | GRCh38.p7 | 10:101535518 | ATCAATATTATGCTC[C/T]CATTCATTATTAATG | 8945 |
rs758090024 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352228 | CTCCATTTTGCACTT[A/G]TGTAGAATTTTTTTA | 8945 |
rs758104561 | snp | A/G | 1.65157e-05 | 0.0028736 | intron-variant | BTRC | GRCh38.p7 | 10:101533085 | GGTAGAAAATTTCAA[A/G]TGCTTTTTTGAACTC | 8945 |
rs758112303 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459385 | GTAATCTCATTCACT[A/G]GCATTCTGCTTCTAC | 8945 |
rs758133114 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101528579 | AATCCCATGATAAAC[C/T]CATGAAATTCCAAAT | 8945 |
rs758144838 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490156 | AAAAGTCCATTTTCT[C/T]TTCATGTATCTTCAA | 8945 |
rs758147138 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101437844 | CGTTCTGCTTACCTG[-/A]AAAAAACCCCTCCAC | 8945 |
rs758188536 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431145 | GCAGTGGCGTGATCT[C/T]AGCTCACTGCATCCT | 8945 |
rs758188804 | snp | A/G | 1.6717e-05 | 0.00289106 | intron-variant | BTRC | GRCh38.p7 | 10:101430481 | CTCTGTGGGTTATTT[A/G]CGGGCATTAGTGTAT | 8945 |
rs758199044 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101529628 | ATGCTGGTGTATCAT[A/G]TTTCATTAATCCCCC | 8945 |
rs758228235 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536140 | AAAGAAGTGTCTGCC[A/G]TGGCAGAGGGGGAGG | 8945 |
rs758247448 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505747 | TATCTGAATTTTTCA[A/T]ATTTACTAAAATGTG | 8945 |
rs758252192 | in-del | -/ATAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101436641 | TAGATAGATAGATAG[-/ATAG]ATAGATAGATAGATA | 8945 |
rs758255459 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101390336 | ATGTCCTGGTATGAT[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs758257256 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476297 | TGTGGGATCCTAGAT[G/T]AGATGCTGAACAGAA | 8945 |
rs758271018 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550799 | ACTTCCTAAATGATC[C/T]AGCTGCCCAAGCTGA | 8945 |
rs758310135 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101491342 | GCATGCACTGGCAGT[C/T]CTTTCATACCAACAC | 8945 |
rs758361080 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101498655 | TAGTGGGCACGTCCT[A/C]ATACAGCCTGAATTG | 8945 |
rs758365779 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101376279 | TCAGTGAGCCAAGAT[G/T]ATGCCACTGCACTCC | 8945 |
rs758373190 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514850 | CTACACTTGTGTCCT[C/T]ACACCAAAGCCACAC | 8945 |
rs758376131 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447011 | GGTGGTGGGGGGGCC[A/G]GTTACAAAGCAATAG | 8945 |
rs758390858 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101521512 | GTTTTCCACGTAATT[A/G]CTAATAGAATAACAG | 8945 |
rs758397422 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101427021 | TCAGATTCAATCTTT[-/C]CTTCCGAATGACTGT | 8945 |
rs758402869 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392768 | ACCTCAGGCGATCCA[C/T]CTGCCTCGGCCTCCC | 8945 |
rs758424459 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445659 | TATTTTCTTGCTCTA[C/G]TGACATCAATCCCAT | 8945 |
rs758426146 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532970 | TGGGATAAAAACACA[C/T]TGGAATGCAAGCGAA | 8945 |
rs758446299 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475535 | ACAGAGTGAGACTCC[A/G]TCTCAAAACAAAAAC | 8945 |
rs758517825 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555226 | AAAAGGCATGGGTTT[C/T]GAGCTGTCTCAAAAT | 8945 |
rs758520005 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360961 | CAGGTTTGTGCCACC[A/G]CACCTGGCTATATTT | 8945 |
rs758533701 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101538103 | CTCTTGATCCCAAAG[C/T]ATGGTATAACTTTAC | 8945 |
rs758547618 | in-del | -/TTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101399322 | ATAACTAGAATCACC[-/TTTTT]TTTTTTTTTTTTTTT | 8945 |
rs758549296 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417272 | GATACATTTAGTAGT[C/T]ATACCTCTTTAGTCT | 8945 |
rs758583969 | in-del | -/T | 1.6676e-05 | 0.00288751 | intron-variant | BTRC | GRCh38.p7 | 10:101535346 | CTCAATGCCATTTTC[-/T]TTTTCAGGTATGGAA | 8945 |
rs758606887 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409513 | TCAACATTGTGTGAA[C/T]GTCATCTAGTGTACT | 8945 |
rs758608920 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101471410 | TAGACAGACAGATAG[A/T]TAACTACTTTTTTTT | 8945 |
rs758619003 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378002 | AAATAAGTGAGAAAC[G/T]CTTATGGACACTGTG | 8945 |
rs758619122 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101522919 | ATATTTAAATTCTAC[A/T]GATGGGTTGGGCACG | 8945 |
rs758640824 | snp | A/T | 1.68761e-05 | 0.00290478 | intron-variant | BTRC | GRCh38.p7 | 10:101535322 | CCAATAAAAGCACCA[A/T]ATCAACTGCTCAATG | 8945 |
rs758642861 | snp | A/G | 1.77027e-05 | 0.00297507 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521652 | AGACAAAACTTGCCA[A/G]TGGCACTTCCAGTAT | 8945 |
rs758656060 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389895 | CTTCCAAAGTGTTGA[G/T]ATTATAGGTATGAGC | 8945 |
rs758657114 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101523398 | GGCAGACAAGAACAC[A/T]GCCAAGGTGTCAGTA | 8945 |
rs758657880 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101486775 | AGTTAGCATTTTCTT[A/T]ACAACATGAAATATA | 8945 |
rs758660504 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101548711 | GAGCCGAGATTGCAC[C/T]ACTGCACTCCAGCCT | 8945 |
rs758691647 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493709 | TCTCTTGCACTTATA[A/G]TATTTTCCTTTCTAG | 8945 |
rs758695929 | snp | C/T | 1.65441e-05 | 0.00287607 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521854 | GTTGCAGAGAGATTT[C/T]ATAACTGCTCTGCCA | 8945 |
rs758772476 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425588 | AAGGTAAATATTTAA[A/G]CAGGAGAATGCGTAG | 8945 |
rs758774219 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101455218 | ACTATGCCCAGCTAA[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs758785153 | snp | A/G | 1.65512e-05 | 0.00287669 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531271 | AACAAACCTCCTGAC[A/G]GGAATGCTCCTCCCA | 8945 |
rs758804281 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534865 | CAATGTTGTAGACTT[C/T]GATGACAAGTACATT | 8945 |
rs758811244 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402282 | TCTCTTATGTAATTA[C/T]ATACTTAGTAACCCT | 8945 |
rs758838237 | snp | A/T | 1.77618e-05 | 0.00298003 | intron-variant | BTRC | GRCh38.p7 | 10:101414705 | CAGTGATATTGATGA[A/T]CCTTGCTCTCTGTGG | 8945 |
rs758856328 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358646 | CTTCACTTGGTATTG[A/G]CTGAGGTGTGGGAAA | 8945 |
rs758870076 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359746 | GCTGGGATTACAGGC[A/T]TGCACCACCACACCC | 8945 |
rs758891276 | snp | A/G | | | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550804 | CTAAATGATCCAGCT[A/G]CCCAAGCTGAACCCC | 8945 |
rs758913326 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101442196 | GCTTAGAGGTACTGT[A/G]GAGCTCCACAATGCA | 8945 |
rs758916919 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392124 | AGCTGGGATTACTGG[C/T]GTGCGCCACCACGCC | 8945 |
rs758954080 | snp | A/G | 1.65176e-05 | 0.00287376 | intron-variant | BTRC | GRCh38.p7 | 10:101534635 | TGTAGCTTGAGTACC[A/G]TCTAAATCTCATCTA | 8945 |
rs758960137 | snp | A/C | | | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534799 | ATGGGATATGGCCTC[A/C]CCAACTGACATTACC | 8945 |
rs758970171 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392814 | TAGGTGTAAGCTTCC[A/G]CACCCGACCAATTAA | 8945 |
rs758970801 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369088 | TGGTACTATCCCACC[A/G]TTTTAATTTGTGTTT | 8945 |
rs758984921 | snp | A/C | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405717 | TTGCCTTCAGTGGGA[A/C]ATACAGGATGGAGTG | 8945 |
rs758985463 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463607 | TGTTGAGCACCCACC[A/G]TGAACATGATGCTTA | 8945 |
rs758994591 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386683 | CCAGTGTCACAATTG[A/G]TGACAGCCTGAATTA | 8945 |
rs758999188 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101512803 | TTTCATTTTGTGTGC[C/T]TGTCACCTGACAGCT | 8945 |
rs759032610 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482628 | TCTTGATCTCCTGAC[A/G]TCGTGATCCGCTTGC | 8945 |
rs759036584 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101440992 | AGTTATTGTTGTTTT[A/T]AAGTATTGCTCTGAA | 8945 |
rs759036999 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101552620 | AGCCTCTGCCTTAAT[A/C]TCCAGGCCACATTTC | 8945 |
rs759054228 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444091 | GCAGTCCTAAGGAAA[C/T]GGTATACTTATGTTC | 8945 |
rs759076347 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397155 | GAAATAAAATTCTTA[C/T]ATAAATTCTCTTATT | 8945 |
rs759103744 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101462013 | AGACTGTAATAATGG[C/T]GAACCCCCTAGGAAG | 8945 |
rs759105456 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101413303 | TGCCCACCACCACGC[C/G]TGGCTAATTTTTGTT | 8945 |
rs759141183 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101484448 | AGTGCAACTGTTTCA[C/G]TTTTTTTCCATGCTA | 8945 |
rs759146562 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101444463 | GGACCAGCTCTTGAT[A/G]TAAAAATTCATAGAA | 8945 |
rs759156895 | snp | G/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479383 | ACATACAACAGCTGT[G/T]CCAGACTCTGCTTAA | 8945 |
rs759171596 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549040 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 8945 |
rs759194582 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101483575 | TCCAGCCTGGGCGAC[A/C]GAGTGAGACTCAGTC | 8945 |
rs759229634 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373487 | AATATAGCTGGCATC[A/G]GTCATGTTAAGGGCA | 8945 |
rs759230003 | snp | C/T | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533062 | AGGATCATCGGATTC[C/T]ACGGTCAGGTAGAAA | 8945 |
rs759274821 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536293 | TATGCCTGGAAGAAC[C/G]TGTTTACAGAATTAT | 8945 |
rs759284273 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101400137 | AACATGACACTTGGT[A/C]TTTGAAATTGTTATT | 8945 |
rs759300420 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468613 | ATTCTTGTGTGGGAC[A/G]TGATTTGATGTTACC | 8945 |
rs759306654 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101545459 | ATGATGTCTTAACCA[C/T]CAGTACCTCAGAATG | 8945 |
rs759309445 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445587 | GGTATGTAATAATCG[A/G]CTATTATCGGTCTGT | 8945 |
rs759318098 | in-del | -/AAAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101374787 | TAAAGTATAATAAAT[-/AAAAA]AAAAAAAAAGAAAAG | 8945 |
rs759322466 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101438403 | ACACTCCAGCCTGGG[A/C]GACAGAGCGAGACTG | 8945 |
rs759348557 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452037 | ATTAACGAGGCAGCA[A/G]CAATAACAAGTCAAA | 8945 |
rs759367212 | snp | C/T | 1.65108e-05 | 0.00287317 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526061 | TGTCATACCTGGATG[C/T]CAAATCACTATGTGC | 8945 |
rs759385406 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101414444 | CATACTATTATGTAC[A/G]GTACATAATACTTGA | 8945 |
rs759425310 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353534 | GTGGCGATGGCTTAG[A/G]AGGACCTTGAAATTC | 8945 |
rs759429440 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546363 | CACACCTCTAAATAA[C/T]ACGTAGGTCAAGAAG | 8945 |
rs759435939 | in-del | -/TATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101459319 | AGGTGACTACTTAGG[-/TATA]TATACATGGCTATTT | 8945 |
rs759460473 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358733 | AAAGTGTGGTGGCAA[A/G/T]GTTCTAAGAAGGGAC | 8945 |
rs759462123 | in-del | -/TA | | | intron-variant | BTRC | GRCh38.p7 | 10:101505641 | ATAAAAAAAAAAAAA[-/TA]ATAATAAAAAAACAA | 8945 |
rs759505436 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492705 | AGGTAGTTTCTGAAA[C/T]GTATTGAATTCATAA | 8945 |
rs759505534 | snp | C/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535416 | CAAACGAGGCATTGC[C/G]TGTTTGCAGTACAGG | 8945 |
rs759523330 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101382895 | GAACTTAGACCAATT[-/A]AAAGTGTACTTTTTA | 8945 |
rs759550888 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491652 | CAGTGAGCCAAGATC[A/G]CGCCTCTGCACTCCA | 8945 |
rs759558826 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491191 | TTGGCTCCATATTAC[A/G]TTGTTCTGTATATAA | 8945 |
rs759558863 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506725 | ACCCTAGGTATGCAA[A/G]GTGGATGGCAAGGCT | 8945 |
rs759571192 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101418930 | ACATATTCATTGTAA[A/C]ATGCTTGTCTCAATC | 8945 |
rs759586968 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521922 | ATGATGATAAGAGAA[C/T]TAGATCTCCAGCTAT | 8945 |
rs759594036 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101491970 | GTGTAGTTGTTGTTG[-/TTT]TTTTTTTAACTCCCT | 8945 |
rs759596429 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101367638 | GGAAACCACTCTCTT[A/C]TAATATCTGTAGATT | 8945 |
rs759597402 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101531752 | AAGAAAATCAATCTC[-/TT]TACAGGCGAGTAGGG | 8945 |
rs759597797 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368726 | TGCTCACTTAATATC[A/G]TCTTTTTTGAGGCCG | 8945 |
rs759609043 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530425 | ACAAATAAAGACCTA[A/G]CAAAAGTGATCTCCA | 8945 |
rs759621715 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357004 | TGTGGCAGCGTGCGC[C/T]TGTAGTCCCAGCTAC | 8945 |
rs759623155 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463254 | TTTCACCATGTTGGC[C/T]AGGCTGGTCGCAAAC | 8945 |
rs759629800 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101529512 | CTTCACATTCAAAAT[C/G]TATTATTTGCCTGCA | 8945 |
rs759659508 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514771 | CCATTGAATTATCTT[G/T]GCATCTTTCTTGAAA | 8945 |
rs759664957 | snp | A/G | 8.45788e-05 | 0.00650248 | intron-variant | BTRC | GRCh38.p7 | 10:101535312 | ATAGATTTTACCAAT[A/G]AAAGCACCAAATCAA | 8945 |
rs759674660 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385115 | GTGCACACCTGTAGT[C/T]CCAGCTACTTGCTTT | 8945 |
rs759679547 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547527 | TGTATTTTTAGTAGA[A/G]ACTGGGTTTCTGCTT | 8945 |
rs759701102 | snp | A/C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101446935 | AGGGAGAAGGATACA[A/C/G]GATTGATTTTTTTAT | 8945 |
rs759702682 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101506721 | ACTAACCCTAGGTAT[G/T]CAAGGTGGATGGCAA | 8945 |
rs759718816 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101460062 | ATCTTACACTGAATT[-/A]AACAGGTTTAGTTTA | 8945 |
rs759722138 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101535685 | TTTCTCCTGTCTACC[A/G/T]TTGAAAAGTGCTAAT | 8945 |
rs759728534 | snp | A/G | | | intron-variant, missense | BTRC | GRCh38.p7 | 10:101515911 | TCTTTTTTAATAGGT[A/G]TAGGAGTCACTCTCA | 8945 |
rs759772981 | snp | A/G | 1.65002e-05 | 0.00287225 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430396 | AGCCTGGCGGACAGC[A/G]TGCCTTCGCTGCGAT | 8945 |
rs759782100 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377765 | TAAAAAGGAGTTTGT[A/G]CTATTGAATATTCAT | 8945 |
rs759815281 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409308 | TCTGGACATTTCATA[C/T]AAATGGAAGCATACA | 8945 |
rs759826592 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101540926 | GTTGTAGCTTTTAGT[A/G]TAAAGGTTTTGCACA | 8945 |
rs759829844 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537731 | TGCTTTGGGACAGCC[A/G]TCACTGTTACAACCT | 8945 |
rs759848351 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546264 | ACAAGAGTAGAAATC[A/G]TACAGCATATGCTCT | 8945 |
rs759857692 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434479 | AGTTAACATGTATAA[A/T]ACTAATAGAAAATGT | 8945 |
rs759857877 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101500291 | AATACTGTACGCAAT[C/T]ATAACATGATGGTGT | 8945 |
rs759877896 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101407869 | CTGGGACTACAGGTG[C/T]GTACCACCATGCCCA | 8945 |
rs759877944 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424683 | TCCAGACAGCCAAGT[A/G]TAGGGGGAAGAGTTG | 8945 |
rs759880829 | snp | C/T | 1.67393e-05 | 0.00289299 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532309 | GACAATAGAATCTAA[C/T]TGGAGATGTGGAAGA | 8945 |
rs759882813 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355338 | AAGCACAGTGTGAGC[A/G]AAGATTGGATTTTGT | 8945 |
rs759891950 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101395450 | TGTCTAGGAGTTCCT[C/T]ATTTTCCTGAGTGTG | 8945 |
rs759907473 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101541850 | CTTTTTAAGGATTTT[-/TG]TGTGTGTGTGTGTAT | 8945 |
rs759930076 | snp | A/G | 1.65723e-05 | 0.00287852 | intron-variant | BTRC | GRCh38.p7 | 10:101532902 | GACCAACAAGTCTCC[A/G]CAGCACCCCATCATC | 8945 |
rs759930799 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101501413 | GCAGATACTTCCCCC[A/C]GGTTGTATGGCTAAT | 8945 |
rs759932126 | snp | C/T | 1.77565e-05 | 0.00297958 | intron-variant | BTRC | GRCh38.p7 | 10:101414693 | GAAGGTAGAAGACAG[C/T]GATATTGATGATCCT | 8945 |
rs759934787 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539885 | TGGTTTAATTCGTGT[A/G]TCTCTAATGATTAAT | 8945 |
rs759936642 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371535 | TTTAAGTAGAATCAT[A/T]CAGTGTTTGCCTTTT | 8945 |
rs759939844 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557115 | CATGTAAGCTTCCCC[C/G]AGAGCTTTCAGCTGG | 8945 |
rs759965902 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101486241 | ATTTGTTAGACACTC[C/T]GCATAATGTAACAAT | 8945 |
rs759986126 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555576 | ACCAGTTTGTTGTAG[A/G]AGAAATAATCAGGTA | 8945 |
rs760062383 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404505 | TTTTGTTTAAATTGT[A/G]TTGAAAATGTTGATA | 8945 |
rs760068322 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472366 | AGAGATGGGGTCTCT[C/T]CCTATGTTGTCCAGG | 8945 |
rs760068710 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101457541 | TAGTAACTGAAATTG[C/T]GTGAGTGAAACTGTG | 8945 |
rs760069732 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101379453 | TTAGACCTGTTCTTT[C/T]TCAATGTGTCTTTAA | 8945 |
rs760082049 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101418133 | GCACTTTGAGAGGCC[A/G]AGGCAGGTGGGTCAT | 8945 |
rs760083254 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434201 | GTAATATCTGACCTG[A/G]CATAGGTATATAGTT | 8945 |
rs760088185 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538345 | CCCCGTGCTCCTGCA[C/G]GGACACTCTGTCTAC | 8945 |
rs760088874 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101550461 | GCTAACTTTTTGTAT[A/T]TTTATAGAGATGGGG | 8945 |
rs760097135 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392155 | CAGCTAATTTTTGTA[C/T]TTTTGATAGCGACTG | 8945 |
rs760100938 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101525804 | TCTAAAGGAAGATGG[A/C]AAATACTGTTCATTT | 8945 |
rs760121290 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470788 | AAATTAATTCTTATA[C/T]GTGCCATGAAGTAGA | 8945 |
rs760129765 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526080 | ATCACTATGTGCTGC[C/T]GAACTTGTGTGCAAG | 8945 |
rs760133138 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524615 | AAGACTTATTTATAG[A/G]TACATGGTGAAATGA | 8945 |
rs760143564 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101404999 | CTAGAATCCATCTTA[-/AA]AAAAAAAAAAAAAAA | 8945 |
rs760182492 | in-del | -/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101420075 | ATATATATATATATA[-/TC]ATGAATATATTATTT | 8945 |
rs760182566 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101364819 | TATTTCTTTTAATTC[-/TT]TTTTTTTTTTTTTTG | 8945 |
rs760243876 | snp | A/G | 1.65466e-05 | 0.00287628 | intron-variant | BTRC | GRCh38.p7 | 10:101532920 | GCACCCCATCATCAC[A/G]TTGATCAAAAGGATC | 8945 |
rs760305096 | in-del | -/TTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101387531 | CCTTCATGGGACTTT[-/TTTT]TTTTTTTTTTTTTTT | 8945 |
rs760315977 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393378 | ACCCCAACTTGAAGC[C/T]AGTCAGTCAGAAGCT | 8945 |
rs760331123 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101482317 | TGAGCCACTGTGCCT[A/G]GCCAAGTTTTTTCTT | 8945 |
rs760364871 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483400 | GAGTTCAAGACCAGC[C/T]CAACCAACATGGTGA | 8945 |
rs760374736 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389969 | TTGGCTGTTTTCTCC[A/G]ACTCTGACTTTTTGG | 8945 |
rs760375120 | snp | A/T | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521818 | CCAACATGGGCACAT[A/T]AACTCGTATCTTAAA | 8945 |
rs760377787 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101357121 | CGACAGAGCAAGACT[-/C]CCGTCTCAAAAAAAC | 8945 |
rs760378081 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101466068 | TACATGAAAGTACTC[A/C]TTACTTTTTGAAAAT | 8945 |
rs760439149 | snp | G/T | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557463 | AGGGCTGGATGCTGT[G/T]GATGAGTGTGGGGTC | 8945 |
rs760451897 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356912 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATCG | 8945 |
rs760470937 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550763 | TCAGTAGTTCACATG[A/G]TGACACAATCCTCAT | 8945 |
rs760516305 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398491 | GTATTTTTTAGTAGA[G/T]ACTGGGTTTCATCGT | 8945 |
rs760535277 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415304 | CTGCAGTCTCCCGAG[A/T]AGCTGGGACTACAGG | 8945 |
rs760539510 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428265 | TAGAAGATTAGAGAA[A/G]GTGAGTTGATGTTGG | 8945 |
rs760546217 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101519555 | GCAAACTCTGTGCTT[A/G]TAAAGCCTCATACGA | 8945 |
rs760553068 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358479 | AGTAGCTTGAAATAG[A/G]TGAAATAATTTTAGA | 8945 |
rs760559947 | snp | C/T | 1.82744e-05 | 0.00302272 | intron-variant | BTRC | GRCh38.p7 | 10:101521906 | AAACCATTAATTTGC[C/T]ATGATGATAAGAGAA | 8945 |
rs760605692 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101371382 | GAAGTTCACCATGTT[A/G]GCCAGGCTGGTCTTG | 8945 |
rs760613122 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534810 | CCTCCCCAACTGACA[A/T]TACCCTCCGGAGGGT | 8945 |
rs760624980 | in-del | -/TTTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101412571 | ACTTTAGAGTTTAAT[-/TTTA]TTTAAACTTAATGTA | 8945 |
rs760686960 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517466 | AAAATAAGGCAAGCC[C/T]GAGCCTTGAAATGAA | 8945 |
rs760707197 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101489708 | AAGTTTCTATGAAAA[C/T]AAAATTGTATTTTTT | 8945 |
rs760746688 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520420 | GAGACTGTCATTTTT[A/G]TTCACTGTTATATTC | 8945 |
rs760756088 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101545104 | TTTCAGCACTTTAAT[G/T]ATGTCATTCCATTTT | 8945 |
rs760763226 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101450929 | GTTATTAATATATGT[A/G]CTCAGTAACTATTAA | 8945 |
rs760790382 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491111 | TCAGTAATTCCATGT[A/G]ACTTAAATAGTCACC | 8945 |
rs760811873 | in-del | -/TTAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101457815 | CATTTTATTATGGAT[-/TTAA]TTAATTAATTTTTTA | 8945 |
rs760833560 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101477289 | TACAGGTGTTAGCCA[C/T]CAGGCCCCACCGTGA | 8945 |
rs760843942 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538334 | CTGCTTTGGACCCCC[A/G]TGCTCCTGCAGGGAC | 8945 |
rs760847771 | snp | C/T | 1.65556e-05 | 0.00287707 | synonymous-codon, intron-variant | BTRC | GRCh38.p7 | 10:101531267 | CAAAAACAAACCTCC[C/T]GACGGGAATGCTCCT | 8945 |
rs760860376 | in-del | -/GA | | | intron-variant | BTRC | GRCh38.p7 | 10:101496048 | TATTTCACTGTTTTT[-/GA]GAGTCATTTATATTG | 8945 |
rs760864543 | snp | A/G | 0.000102056 | 0.00714267 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354263 | CGGGGAACGGTGGAG[A/G]CGCTGGCGTTGGCGG | 8945 |
rs760881547 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487281 | TACTTTCTTATGCCA[A/G]CCCATTTCTTCATTG | 8945 |
rs760918133 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445733 | AATAATTGATAAACC[A/G]GATAAGATTTAAACT | 8945 |
rs760929131 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367469 | ACAAATAGTTACATA[C/T]TTTTAATATGTACAA | 8945 |
rs760940097 | in-del | -/TGAAGT | | | intron-variant | BTRC | GRCh38.p7 | 10:101493038 | TGCCCTTGAAACTTC[-/TGAAGT]TGGAGGTTTCAATTG | 8945 |
rs760949504 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406846 | GCCTCAGCTTTCTTA[C/T]GACTGTTTTTATGAT | 8945 |
rs760962629 | snp | A/C | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407688 | AGCCACTGTGCCCAG[A/C]CTAACACAGTGTAGT | 8945 |
rs760988664 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393654 | CAAAAACAACCCACA[C/T]TTGGTCACAGAGAAG | 8945 |
rs761006699 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459697 | AGCTCTGTGTTCTAT[G/T]TTAGGTTAGTAACAC | 8945 |
rs761016296 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368581 | AACTCCTGGGTTCAA[A/G]CTGTCTTCCCATTTT | 8945 |
rs761062749 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101504857 | TCTGATCAATTTGAT[A/G]TTATGAACAAAGAAT | 8945 |
rs761063915 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353839 | CTTAGAGGCTGTAAA[C/T]TACAATTCCCATCAG | 8945 |
rs761087342 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554369 | TGCCAAGACCGTGAT[C/G]AAGGTAGCTTAAGAG | 8945 |
rs761108680 | in-del | -/AG | 1.65021e-05 | 0.00287241 | frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521843 | TTAAACCTATGTTGC[-/AG]AGAGAGATTTCATAA | 8945 |
rs761127904 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101371093 | CTTTTTTGTCTTGCA[A/G]AACTGAAACTCTATA | 8945 |
rs761148097 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101394165 | GGGCATGTTGAATTT[A/T]TTTATGAAAGAAGGG | 8945 |
rs761181460 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432355 | CTGGTATCGAACTCC[C/T]CAGCTCAAGTGATCT | 8945 |
rs761203862 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101469168 | GGGACAGAACCTATC[A/T]TGCCTGTGGCTATTA | 8945 |
rs761204606 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470609 | TGCTGGGATTACAGG[C/T]GCGAGCCACCGCGCC | 8945 |
rs761237744 | in-del | -/GTACCGCGGGCACACAACACCAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101552316 | GCCTCAGCCTCCTGA[-/GTACCGCGGGCACACAACACCAT]GACCAGCTAATTGTT | 8945 |
rs761242363 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524331 | TTCTCCCCAGTCACT[A/G]AGACATGTTACTATC | 8945 |
rs761253734 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433870 | CCAGGATCTTTAAAT[A/T]CTTAAAAAATTATTG | 8945 |
rs761272728 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101500230 | AGGCTATATGGTATA[A/C]CTATTACTCCTAGGC | 8945 |
rs761279905 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101537514 | GCCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA | 8945 |
rs761284278 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447031 | CAAAGCAATAGAAGC[A/G]TGCAGCTAGTGTTCG | 8945 |
rs761304355 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446913 | TTTGTATTCCAGAGA[G/T]CACAATAGGGAGAAG | 8945 |
rs761311684 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507036 | ATATGCTGACTGAAC[A/G]TTTAATAAGATAACC | 8945 |
rs761324748 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525387 | TACTCTCAAATATAG[-/T]TTTTTTTAAATCTGA | 8945 |
rs761332325 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101522963 | GTAATTCCAGCACTT[C/T]GGGAGGCCGAAGTGG | 8945 |
rs761371090 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377490 | ACCAGTTGGCATTCC[C/T]ACAAGCAATGGGTGA | 8945 |
rs761383071 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | BTRC | GRCh38.p7 | 10:101538379 | CCCTTGTGGTAAGAG[C/T]CTTGCTGTTTAGAGA | 8945 |
rs761400651 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527556 | CCAGGAGTTTGATAC[C/G]AGGCTGGGCAACATA | 8945 |
rs761404337 | in-del | -/TTCTCTTCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101472315 | TTCTCTTCTCTTCTC[-/TTCTCTTCT]CTCTCTTCTTTCTTT | 8945 |
rs761433031 | in-del | -/ATATAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101475938 | TATATATATATATAT[-/ATATAT]ATATATATATATATA | 8945 |
rs761437730 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101455506 | GTGAAGTTTTTCTTC[A/G]GAGTAATTAATTCTA | 8945 |
rs761447032 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360559 | TTGTATTTTTGTAGA[C/T]GGGGTTTCACCATGT | 8945 |
rs761469616 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457244 | AGATGAAGTGAGGTA[A/G]ATGACCTAGGCATTG | 8945 |
rs761471014 | snp | A/G | 0.000164791 | 0.00907569 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521812 | TCATTACCAACATGG[A/G]CACATAAACTCGTAT | 8945 |
rs761472691 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510052 | ATGTCTGTAATCCCA[A/G]CTACCTGGGAGGCGG | 8945 |
rs761480891 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554088 | GGAGAAGTTTCCTGG[A/G]CTCCATCAATGGCTG | 8945 |
rs761488999 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101391720 | AATATTTTTACTTCT[A/T]AATTTGCAAATTGCA | 8945 |
rs761489972 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101494694 | CATGTTTCTTTCAGG[A/T]TGAGAAAGATTTGAA | 8945 |
rs761501071 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359332 | GTGTATACTTTACCT[A/T]TTCCCAGTTTAAATT | 8945 |
rs761513708 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547928 | ATATCAATGGATGCA[A/G]TAAAAGCATTTGACA | 8945 |
rs761544432 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403111 | TAAAATTTCTAAGCA[C/T]TGATGGCATTGTTGG | 8945 |
rs761569179 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465648 | ATAGAGAAGGAAAGA[A/G]CACTCCTTGACTTAA | 8945 |
rs761577474 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534801 | GGGATATGGCCTCCC[C/T]AACTGACATTACCCT | 8945 |
rs761579157 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101388647 | GGTGCCCACCACCAC[A/G]CTTGGCTAATTTTTT | 8945 |
rs761599586 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101417921 | GGCCTCAGGCAATCT[A/G]CTGGGTTACAGGTGT | 8945 |
rs761599728 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101401694 | TTAAGAAAAAGAGGC[C/T]GCTTGCAGTGGCTCA | 8945 |
rs761627312 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369638 | AAGCGTGCTCATTGC[A/T]ATTGGGGTGTCACTG | 8945 |
rs761628536 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425164 | CTTAGTATTCCATGG[G/T]ATATGTGTACTGCAT | 8945 |
rs761635802 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371088 | TAGAACTTTTTTGTC[G/T]TGCAAAACTGAAACT | 8945 |
rs761652283 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411364 | ATATTTGGAAATATG[C/T]ATTTTCCAAATATAT | 8945 |
rs761654945 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554248 | AAGGCTCAGCCTACA[-/G]AAAGATTTGAAATGG | 8945 |
rs761657202 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101462450 | TTTGGGAGGCTGAGG[C/G]AGGCGAATACCTGAA | 8945 |
rs761703126 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517051 | CTAAATCTTCACATT[G/T]CATGAGTTTTCATTT | 8945 |
rs761710060 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101550300 | TTTATTTTATTTTTT[C/T]TTTAGACAGAGTCTC | 8945 |
rs761791926 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465076 | GCATATGACAATAAT[C/G]AAGTGCCATTTGCTA | 8945 |
rs761793086 | in-del | -/TGTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101412314 | GGTCCCATTGTACTC[-/TGTT]TGAGTTCCCCTTTCT | 8945 |
rs761865382 | snp | C/T | 1.77505e-05 | 0.00297908 | intron-variant | BTRC | GRCh38.p7 | 10:101414662 | CTCCCAAAGACCTTC[C/T]AGTGCCATAAGCTAT | 8945 |
rs761872007 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488306 | TCTGTTTATTAGAAA[C/T]TTGCTGTTTTGTTTT | 8945 |
rs761876783 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436589 | CACTGCATTCTAGCC[C/T]GGGTGACAGAGTGAG | 8945 |
rs761883378 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427141 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGTTCTGT | 8945 |
rs761908633 | in-del | -/TTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101444304 | ATAGATTTTCAATCC[-/TTG]TTGTCTTCAGAACTG | 8945 |
rs761916228 | in-del | -/TAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101426203 | ACTCCATTTATTTTG[-/TAA]TAATATTTTTTCTCA | 8945 |
rs761939940 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101376707 | TGGCATCTTTACATA[A/G]AGGAAAAGGATGTAA | 8945 |
rs761942081 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503393 | AAAACTGTTCAGCTT[A/G]TATAATAACTGCATT | 8945 |
rs761948466 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526106 | GCAAGGAATGGTACC[A/G]AGTGACCTCTGATGG | 8945 |
rs761949817 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356881 | TCATGCCTGTAATCC[A/G]GGACTTTGGGAGGCC | 8945 |
rs761953330 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101450642 | ATAGGTAGTACAGCC[A/G]AGTTGTTCAGTTTTC | 8945 |
rs761966499 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412456 | TCAGTGTCTTGAAAT[A/G]TATGTTTCACATATT | 8945 |
rs761977020 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101455083 | TTTTTTTTCTTTGAG[A/G]CAGGGTCTCACTCTG | 8945 |
rs761980921 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101519492 | GCAGCTAGAGACTGA[A/C]CACATTCCTTGCCAG | 8945 |
rs761989538 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101379443 | TTTATCTCATTTAGA[A/C]CTGTTCTTTTTCAAT | 8945 |
rs762012584 | snp | A/C | 0.000412116 | 0.0143488 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354202 | CCGGCCGAGGCGGTG[A/C]TGCAAGAGAAGGCAC | 8945 |
rs762020772 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514777 | AATTATCTTGGCATC[C/T]TTCTTGAAAGTCAGT | 8945 |
rs762041956 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457470 | ACCAGAAAGGTGCAC[A/G]ATTGAAAACTATTTC | 8945 |
rs762051700 | in-del | -/TTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101383061 | CTTCCCTGGAGATTT[-/TTTTT]TTTTTTTTTTTTTTC | 8945 |
rs762104685 | snp | A/G | 1.65274e-05 | 0.00287462 | intron-variant | BTRC | GRCh38.p7 | 10:101536675 | GTGCTAACAGAGTGT[A/G]AAAAAGAGAAAATCT | 8945 |
rs762107555 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533372 | CAAAAACCACCTCAC[A/G]GGGGAATGATATGAA | 8945 |
rs762127039 | in-del | -/CTTTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101486772 | TGGAGTTAGCATTTT[-/CTTTA]CAACATGAAATATAT | 8945 |
rs762189757 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498864 | TGGGTGTAGTGGTGC[A/G]CGCCTGTAATCCCAG | 8945 |
rs762230256 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531034 | AAAATTAGCCAGCAT[A/G]GTGGCAGATGACTGT | 8945 |
rs762240183 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101400761 | AAACATGTAAATCCA[C/T]CTAGGGGAAGAAAAG | 8945 |
rs762264873 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101552875 | GGGCAAGTGAAAGCT[A/G]TGCCAACCGTGGGCA | 8945 |
rs762265700 | snp | C/G | 1.6563e-05 | 0.00287771 | intron-variant | BTRC | GRCh38.p7 | 10:101479360 | TTTCCAACAAATTCT[C/G]TTTACAGACATACAA | 8945 |
rs762301484 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392277 | GCCACTGCACCCAGT[A/G]AAAACATTCTTAAAT | 8945 |
rs762314545 | in-del | -/GGG | | | intron-variant | BTRC | GRCh38.p7 | 10:101394178 | TTTTTTATGAAAGAA[-/GGG]GACTCTGGTAATTAA | 8945 |
rs762325011 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364566 | GCTGATATATTTAGA[A/T]GTCTGGAAAACTTTC | 8945 |
rs762350938 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405851 | AACTTCCTTCATGGC[C/T]CATCTTAAGGTCTGT | 8945 |
rs762351265 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484615 | CAGGCTTCTTTAAGA[C/T]ACTGTTCCACAAGTA | 8945 |
rs762358776 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101397313 | AGATAAGCTGCATCC[G/T]GTTGTCATGGCAACC | 8945 |
rs762361540 | snp | A/G | 3.95202e-05 | 0.00444506 | intron-variant | BTRC | GRCh38.p7 | 10:101521604 | CTCATTTTCAATACT[A/G]ATCATTTTATGTTTC | 8945 |
rs762365415 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520871 | CTGAGGCAGGAGAAT[C/T]GCTTGATTCTCCGCC | 8945 |
rs762370310 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533053 | GATCATAACAGGATC[A/G]TCGGATTCCACGGTC | 8945 |
rs762401473 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352786 | CAGTAGCGTGATCTC[A/G]GCTCACTGCAACTTC | 8945 |
rs762441989 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459824 | AAAGAAAATTGTGAG[A/T]ATGGGCTAGTCAATA | 8945 |
rs762456936 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393464 | TCTCAAGATGAGGCC[C/T]GAGGCTCTCTTTTAA | 8945 |
rs762461197 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536342 | AAAATACATTTTACA[G/T]TTGAACTTAAACCTA | 8945 |
rs762466133 | snp | C/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514587 | CTGCCCTAGTAGCTA[C/G]GATTATAGGCGTGTG | 8945 |
rs762497337 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101477253 | TGATCCTCCTGCCTT[C/G]GCCCCCCAAAGTGCT | 8945 |
rs762512554 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400221 | AATACACTGCTGAAA[A/G]TGAGTTTCTTCTTTG | 8945 |
rs762534249 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373684 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 8945 |
rs762535279 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505760 | CATATTTACTAAAAT[A/G]TGTCTACTGTAAATG | 8945 |
rs762605128 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534780 | AAGATCGTTCCATTG[C/T]TGTATGGGATATGGC | 8945 |
rs762652665 | in-del | -/C | 1.65531e-05 | 0.00287686 | intron-variant | BTRC | GRCh38.p7 | 10:101462077 | TGAAATTCAGCCTTA[-/C]TTAAAATAAAAAGCT | 8945 |
rs762677464 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479402 | GACTCTGCTTAAACC[A/G]AGAAACAGTATGTTT | 8945 |
rs762694519 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416632 | AGTCTTTGGCTCCAC[A/G]GCATCATGAGACTGC | 8945 |
rs762696153 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101524832 | GCTTATGCTTACATA[C/T]GAACATGTGATGCCA | 8945 |
rs762717271 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417077 | ACCTCTGAATTCTCT[G/T]TGTATTTCCTGCAAA | 8945 |
rs762721846 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101495417 | CATATCATAGCAACA[A/G]TTAAAGCAAATTAAA | 8945 |
rs762740455 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101447093 | AGACCAGACGAGTAG[-/CT]TATCTTGAGGGACGC | 8945 |
rs762745660 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432063 | TCGTTATAAACATTA[C/T]TGCTATTATTGGAGA | 8945 |
rs762745871 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414993 | ATGTTTTAATAAATT[C/T]AGTCTAGCCTAAGTG | 8945 |
rs762765734 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387678 | ATTACAGGTGCCCAC[C/T]ACCACACCCGGCTGA | 8945 |
rs762766101 | snp | C/G | 0.000107256 | 0.00732232 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354174 | GGACCCAGTGGCCTC[C/G]GCGATTATGGACCCG | 8945 |
rs762776691 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101492115 | ACCATGACAAACAGG[A/C]ACAGCAAAATATTTC | 8945 |
rs762792474 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424984 | TGTATTCCTCAGTGT[C/T]TGTTCCCTTCTTTAT | 8945 |
rs762822898 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101401292 | GAGCATTCAAAAATA[C/T]AGAAATTCTTTACTT | 8945 |
rs762828910 | in-del | -/TCAC | | | intron-variant | BTRC | GRCh38.p7 | 10:101526382 | TTTTCTTCTTACCTG[-/TCAC]TCACAAAATGACATG | 8945 |
rs762839804 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530808 | TACCTTTGCTCCTCC[G/T]CAGACAGCTATGGAG | 8945 |
rs762847568 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101506820 | CAAAGGGTTAAATTA[C/T]GTAGTTAGTGAATGC | 8945 |
rs762871853 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101361589 | GGGGAAGAAATCTCT[A/G]TGGGAAGGGTCCACT | 8945 |
rs762883482 | in-del | -/TTTT/TTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101359604 | GCTAATTTTGTTGTA[-/TTTT/TTTTT]TTTTTTTTTTTTTGA | 8945 |
rs762884724 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101511110 | TCCTTTACACTTCAG[A/G]TGAAATCTAAACTCT | 8945 |
rs762953086 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516982 | GAGGTTTTCATTATT[A/G]GGATTAGAAGTGGCA | 8945 |
rs762962983 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101539192 | CCTTTTGACATTTGG[G/T]GAAAAAAGTGATTCA | 8945 |
rs762966257 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101422550 | TCCTTGCCCATGCCT[A/G]TGTCCTGAATGGTAT | 8945 |
rs762980501 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461468 | CAAGGAATGGACTCT[A/G]ATCCTAAACTACTGA | 8945 |
rs762988489 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101391005 | TTTAGAAATTTTACT[C/G]TTGATAATTAAAGTT | 8945 |
rs762989137 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101494500 | AAAAAATATTTTCTT[A/G]ATTTTGAGAATGCGG | 8945 |
rs763016312 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500297 | GTACGCAATCATAAC[A/G]TGATGGTGTTTGTGT | 8945 |
rs763043127 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516013 | GGTGTTGGTTATGTG[A/G]GTATGTTCACCTTGT | 8945 |
rs763046827 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101488259 | TCCAGGCAGCCAGCT[A/C]TGTCATATTTAAATT | 8945 |
rs763048606 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557067 | TCTGAGGGATGGCCA[A/G]TGCACTCCAATGATG | 8945 |
rs763077789 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | BTRC | GRCh38.p7 | 10:101354077 | GAGAGGTAAGAGAGG[A/G]CGGGGGGAAGGAAGA | 8945 |
rs763077864 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369391 | TTGTGTGCCAGGACT[C/T]CTTATTTATTTTGAT | 8945 |
rs763087404 | snp | C/T | 3.33106e-05 | 0.00408095 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535452 | GCTGGTAGTGAGTGG[C/T]TCATCTGACAACACT | 8945 |
rs763102118 | snp | A/G | | | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538309 | AAAATTAAAGTGTGG[A/G]ATCTTGTGGCTGCTT | 8945 |
rs763109497 | snp | C/T | 1.99455e-05 | 0.00315791 | intron-variant | BTRC | GRCh38.p7 | 10:101525966 | TTGTAAAAAATCATT[C/T]GCCACCTTCTGTGTT | 8945 |
rs763114494 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531536 | ACCAGCCTGGCTAAC[A/G]TGGTGAGACCCCTGT | 8945 |
rs763118583 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101426399 | ATAATCGGGAATGCA[A/T]CCTCTGTGTGGTGTT | 8945 |
rs763123931 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101405121 | TTTCTTGAGTTCCTC[C/T]CTCTGTACAATCTCC | 8945 |
rs763135920 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101409693 | AGACATAGAAAAGAT[A/G]TAGTTAAAATGTTGG | 8945 |
rs763144829 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101457996 | TCCATTTATGTATTA[-/T]TTTTTCTGAACAATT | 8945 |
rs763180703 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356698 | TGACACCTTAATAAA[A/G]GAAACAGAGAATGGA | 8945 |
rs763208088 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472747 | TTGAACCCGGGAGAC[A/G]GAGGTTGCGGTGAAA | 8945 |
rs763215998 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533041 | TGATGAGAGAGTGAT[C/T]ATAACAGGATCATCG | 8945 |
rs763270900 | snp | C/T | 1.65304e-05 | 0.00287488 | intron-variant | BTRC | GRCh38.p7 | 10:101461964 | AGAACTGAATTAAAG[C/T]TTACTTTCTTTCACA | 8945 |
rs763291199 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101448950 | TGTAATTTTAAAGAC[A/C]CGAAGAGACATTAAG | 8945 |
rs763304635 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394522 | AGTTTCAAAGGTAAA[A/G]CTTAAAGCAGGTCCT | 8945 |
rs763310493 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528570 | TATCCTCTTAATCCC[A/G]TGATAAACCCATGAA | 8945 |
rs763311446 | in-del | -/AATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101418501 | GAAAAATGAATACTT[-/AATA]AATACTTATTTTCAA | 8945 |
rs763326208 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101418551 | GTATTTCAGAGTGCC[A/G]CCTCCCAAAATGACA | 8945 |
rs763327006 | snp | C/T | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532332 | GTGGAAGACATAGTT[C/T]ACAGAGAATTCACTG | 8945 |
rs763328210 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101435127 | GAATTACAGCAGTCT[C/T]AGTGCATTTGCATCC | 8945 |
rs763353554 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101489021 | TAATATTATGCCTCT[A/G]CTTAAAACTCATTGT | 8945 |
rs763367456 | snp | C/T | 0.000148445 | 0.00861397 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430413 | GCCTTCGCTGCGATG[C/T]CTGTATAACCCAGGG | 8945 |
rs763383654 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101428525 | GTTATCTGGTGATGC[-/CT]CTTTAGCAGATACCC | 8945 |
rs763392884 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530825 | AGACAGCTATGGAGA[A/G]TATATGGAATGGTAA | 8945 |
rs763395539 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520988 | AAAAGTTGTGATGAC[A/G]GAGCACAATAGCTCA | 8945 |
rs763426155 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101525187 | TCTGAGACCTCAGTA[A/C]AGATTTGGGTGGTGG | 8945 |
rs763435867 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421251 | ATAACCTCTTGGGTG[C/T]GATTTCTTTATTTAG | 8945 |
rs763436955 | in-del | -/G | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557463 | AGGGCTGGATGCTGT[-/G]GATGAGTGTGGGGTC | 8945 |
rs763487416 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419663 | TGCAGTCTTAACCTA[A/T]TTAGGAAAATGGCAT | 8945 |
rs763490253 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364341 | ATTCCACAGTGATGC[C/T]CTGAAAAGTTCAGCA | 8945 |
rs763507905 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550743 | GTTTGATGAATTCCA[A/G]ATTGTCAGTAGTTCA | 8945 |
rs763524784 | snp | A/C | 1.65822e-05 | 0.00287938 | intron-variant | BTRC | GRCh38.p7 | 10:101532906 | AACAAGTCTCCACAG[A/C]ACCCCATCATCACAT | 8945 |
rs763565745 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511806 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCT | 8945 |
rs763577783 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499300 | GGAGTGCAGTGGTGC[A/G]ATCTGGGCTCACTGC | 8945 |
rs763583896 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479405 | TCTGCTTAAACCAAG[A/G]AACAGTATGTTTAGC | 8945 |
rs763594671 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469080 | ATGCGATATAAAAAC[A/G]TATTAAAGTACTCCA | 8945 |
rs763605614 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527673 | GTGGGAGGATGGCTT[C/G]AGTCTGGGAAGTTGA | 8945 |
rs763652142 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520924 | GCCAAGATCATGCCA[A/G]TGCACTCCAGCCTGG | 8945 |
rs763700509 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521210 | GCCCAGGAGCTGGAG[G/T]CTGCAGTGAGCTATG | 8945 |
rs763766997 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101462680 | GCAAAACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 8945 |
rs763782064 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424319 | TATCCTATCTGACAG[A/G]TGGGAGTTTTGTTTT | 8945 |
rs763786340 | in-del | -/CTAGATGGTGCCACTGCACT | | | intron-variant | BTRC | GRCh38.p7 | 10:101404946 | GAGCTTGCAGTGAGC[-/CTAGATGGTGCCACTGCACT]CCAGCCTGGGTAACA | 8945 |
rs763811574 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101461717 | AAGTGCAAGCTAGAG[A/T]TCTAATGAATATGAT | 8945 |
rs763818635 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491432 | GCCTGGTTCGGCTCA[C/G]ACTTGTAATCCCAGT | 8945 |
rs763842946 | in-del | -/TTTCTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101527283 | AAGTAGTTGGCTCTC[-/TTTCTT]TTTTTCTATCTTTGA | 8945 |
rs763846020 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101529631 | CTGGTGTATCATGTT[G/T]CATTAATCCCCCTTT | 8945 |
rs763848435 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493809 | GAACCTTGTAATCTC[-/T]TTACTGTCTGTTAGG | 8945 |
rs763853582 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419397 | TCACAAGGCCATAAT[C/T]AAGGTGGTGTCTAGG | 8945 |
rs763861221 | snp | C/T | 3.8795e-05 | 0.00440409 | intron-variant | BTRC | GRCh38.p7 | 10:101521607 | ATTTTCAATACTAAT[C/T]ATTTTATGTTTCTTT | 8945 |
rs763862345 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493030 | TTATTTAGTGCCCTT[A/G]AAACTTCTGAAGTTG | 8945 |
rs763883729 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433262 | ATATAGATGTTTATT[A/T]TATTTCTATTTTGTG | 8945 |
rs763901498 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460591 | AAACACATTAGGGTA[C/T]TGGCCTGTCAGGCTT | 8945 |
rs763911624 | in-del | -/CTTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101410932 | TTTTTGCTTAAATTG[-/CTTA]CTTTTTAAAAAAATT | 8945 |
rs763915994 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438865 | CTTGAAAATAACACA[A/T]TATTTGACCAAAATC | 8945 |
rs763917774 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101455269 | GCTATGTTACCCAGG[A/C]TGGTCTTGAACTCCT | 8945 |
rs763929023 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101477925 | AAAGTGTTAGGATTA[C/T]AGGTATGAGCCACCG | 8945 |
rs763943861 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101359157 | TAAGTAAACTTGCTT[A/G]CTTACTTCAGGAAAC | 8945 |
rs763961017 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | BTRC | GRCh38.p7 | 10:101354108 | GGAGGCGGGATCCGG[A/G]CGCTGCGTTGGCTGC | 8945 |
rs763961115 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369474 | CTGTTTTTTGGTGTC[A/G]TTGAGCATTTTCTTG | 8945 |
rs763993265 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101467405 | TTAGAAGGTACACAC[A/C]GCCAAGGGAGCTTTG | 8945 |
rs764054969 | snp | C/T | 8.25975e-05 | 0.00642588 | intron-variant | BTRC | GRCh38.p7 | 10:101533086 | GTAGAAAATTTCAAA[C/T]GCTTTTTTGAACTCT | 8945 |
rs764055447 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101409818 | GTTTATTCGTTGATA[A/C]GTATTTTTGGGCTGT | 8945 |
rs764072289 | in-del | -/GTGA | | | intron-variant | BTRC | GRCh38.p7 | 10:101382821 | CTCAATTTTGAAATG[-/GTGA]GTGTTTCCTATTTTG | 8945 |
rs764080042 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554845 | CACCCAGCTGGTCTC[C/T]CCAGGCAAGAAGGTA | 8945 |
rs764081492 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101368901 | GCGGGCACCTGTAAT[C/G]CCAGCTACTCAGGAG | 8945 |
rs764121893 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101530816 | CTCCTCCGCAGACAG[A/C]TATGGAGAGTATATG | 8945 |
rs764122418 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555777 | CAGAGCTGAAGGTGT[C/T]CCCATTGTAGATTAG | 8945 |
rs764144927 | in-del | -/CATT | | | intron-variant | BTRC | GRCh38.p7 | 10:101433665 | TGAGGTCTTATGGGC[-/CATT]CAAAGTGTGTAGTTT | 8945 |
rs764158377 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101479895 | AATGTTGGAAATACT[A/G]CTTTTGTTGATCTTG | 8945 |
rs764163950 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500342 | AAACATAGAAAAGGT[A/G]TAGTAAGAATACAAT | 8945 |
rs764168551 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539289 | TCCATTAGAAAATTA[C/G]TTGGAGCAACAGGGT | 8945 |
rs764236622 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434427 | TACTGCACTATATAC[A/G]TAAATTAATTTGAAA | 8945 |
rs764257625 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101418564 | CCACCTCCCAAAATG[A/G]CAGCATGATATACCT | 8945 |
rs764265523 | snp | A/G | 1.65471e-05 | 0.00287633 | intron-variant | BTRC | GRCh38.p7 | 10:101536515 | AAAGAATACGTGAAA[A/G]TTCACCTGACTTAAT | 8945 |
rs764295137 | snp | G/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526085 | TATGTGCTGCTGAAC[G/T]TGTGTGCAAGGAATG | 8945 |
rs764299997 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101473882 | GGATTACAGGCATGA[A/G]CCACCATGCGCAGCC | 8945 |
rs764319809 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101463346 | ACTGTTCCCGACCTA[A/C]TTTTTGTATTTTTAG | 8945 |
rs764342156 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101379668 | AGAAATCTTTGTTTA[A/T]AGTGGCACTCGTTTT | 8945 |
rs764348002 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525201 | ACAGATTTGGGTGGT[A/G]GAGAACTTTAATTGG | 8945 |
rs764369310 | snp | A/T | 1.67942e-05 | 0.00289772 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535465 | GGCTCATCTGACAAC[A/T]CTATCAGGTGAGCAG | 8945 |
rs764375145 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452020 | TTGTCAAAGGCATTC[A/G]GATTAACGAGGCAGC | 8945 |
rs764415335 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403470 | TGTTGAGGATTTTTG[C/T]CTATATGGCCATAAG | 8945 |
rs764416478 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101454747 | TGATCATGTCATTAC[A/G]CTCCAGCCTGATGTG | 8945 |
rs764417257 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419885 | CACCTCAAGAAGATA[C/T]TCCAAGCTCCTCTTA | 8945 |
rs764421460 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101396679 | TTGTTTGTGAAAGTC[-/TG]TGGAAACATCAGTCA | 8945 |
rs764455328 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101482008 | ACCCATAGCATGAGA[-/AT]ATACTGAAAAAGGTT | 8945 |
rs764456335 | snp | G/T | 1.98304e-05 | 0.00314878 | intron-variant | BTRC | GRCh38.p7 | 10:101525967 | TGTAAAAAATCATTC[G/T]CCACCTTCTGTGTTC | 8945 |
rs764464842 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378083 | TAGTAGCATAGATCA[A/T]TGGTATGATTTTAAT | 8945 |
rs764480986 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396527 | CTACTCACTTGTTCT[G/T]TGGTACTCTTAACAA | 8945 |
rs764486032 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101496886 | TCTCCTAAACTGTGA[C/T]TTGCCTTTTCACTTT | 8945 |
rs764509406 | in-del | -/CC | | | intron-variant | BTRC | GRCh38.p7 | 10:101390354 | TTTTTTTTTTTTTTT[-/CC]GAGACGGAGTCTCGC | 8945 |
rs764538656 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363552 | CCACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 8945 |
rs764547762 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364516 | AGCTTTCCATCTCTT[C/T]GCTGCACCTAAACTT | 8945 |
rs764561828 | snp | A/G | 3.29946e-05 | 0.00406155 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430425 | ATGCCTGTATAACCC[A/G]GGGACTGGCGCACTC | 8945 |
rs764581783 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472791 | CGCTTGTCTCCTAGC[C/T]TTCATTTTTTTATGA | 8945 |
rs764612086 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101526563 | GGTGGGCAGATCACT[C/T]GAGGCCAGGAGTTTG | 8945 |
rs764648305 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404624 | AGCCTTTGCAGTTCT[A/G]TTGAGATATATTCCA | 8945 |
rs764659213 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101502179 | GTCTTTGCTGATTCT[A/G]AAACAATGCCACAAA | 8945 |
rs764664989 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101466588 | AAGCTTCCATCCTCT[C/T]CAAGGATACTTTGCA | 8945 |
rs764670792 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483589 | CAGAGTGAGACTCAG[C/T]CTCAAAAAAAAAACT | 8945 |
rs764713374 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530906 | CGGCCGGGTGTGATG[A/G]CTCACGCCTGTAATC | 8945 |
rs764716778 | in-del | -/TTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101383058 | GGCCTTCCCTGGAGA[-/TTTTTTTT]TTTTTTTTTTTTTTC | 8945 |
rs764739204 | in-del | AACA/CCTGT | | | intron-variant | BTRC | GRCh38.p7 | 10:101460849 | AAATAAACTAACCCT[AACA/CCTGT]TAGAACGTTATGACT | 8945 |
rs764748530 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543234 | CTTAGGATTTTTGTC[-/T]TAGTGATTAACTGAC | 8945 |
rs764778855 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392172 | TTTGATAGCGACTGG[C/G]TTTCACCATGTTGGT | 8945 |
rs764790468 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533064 | GATCATCGGATTCCA[C/T]GGTCAGGTAGAAAAT | 8945 |
rs764790681 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428469 | ACAAAGTTCAGAGAT[C/T]GTTGGAGTAATTCAA | 8945 |
rs764793129 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101482674 | CAATGGGATTACAGT[C/T]GTGAGCTGCCGCATC | 8945 |
rs764817844 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101398679 | TTGCGTACACTAATA[A/C]CATCATCCTTTGCCC | 8945 |
rs764830944 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536303 | AGAACCTGTTTACAG[A/T]ATTATGTAAAGCCCT | 8945 |
rs764856719 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517812 | TAGGATCTGTCTTCA[C/G]AATATACACTGAATC | 8945 |
rs764868647 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497856 | GAAACCCCATCTCTA[C/T]GAAAAACACAAAAAT | 8945 |
rs764869582 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479385 | ATACAACAGCTGTGC[C/T]AGACTCTGCTTAAAC | 8945 |
rs764903643 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101467458 | CCCATTCCCTATCTG[A/C]CGTTGCTTTGTGTTA | 8945 |
rs764906518 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400163 | TTATTTATTTCATAT[A/G]TTGTAGCTGCCAATC | 8945 |
rs764913826 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101549081 | CCAGACACAAAAGAA[C/T]ACATACTATATGATT | 8945 |
rs764931406 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532785 | GTGTGTGTGTGTGTG[C/T]GTGTGCGCGTGTGCG | 8945 |
rs764944005 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101413343 | TTTTTTGACAGAGTC[C/T]CGCTCTGTTGCCCAG | 8945 |
rs764969445 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504172 | GGTGAACAACCTCCA[C/T]CTGAGGAAGTTACAC | 8945 |
rs764973787 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101519892 | CCCAGCTACTCAGGA[A/G]GCTGAAGCAGGAGAA | 8945 |
rs764984022 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101430522 | CATTAGTATGTGCCT[C/T]CTCCTTTCCCATACT | 8945 |
rs764989488 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant | BTRC | GRCh38.p7 | 10:101534639 | GCTTGAGTACCATCT[A/G]AATCTCATCTATCAC | 8945 |
rs764993284 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452040 | AACGAGGCAGCAGCA[A/G]TAACAAGTCAAATTT | 8945 |
rs764995896 | in-del | -/TTTTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101427133 | TTTTTTTTTTTTTTT[-/TTTTG]AGACGGAGTCTTGTT | 8945 |
rs765023125 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520959 | CAGAGCAAGACTGTC[C/T]CCAAAAACAAAAAAA | 8945 |
rs765029997 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536011 | AGGAAATTATTCCTA[A/G]AAATCACTTGAATTG | 8945 |
rs765030761 | snp | A/G | 3.30126e-05 | 0.00406266 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101462014 | GACTGTAATAATGGC[A/G]AACCCCCTAGGAAGA | 8945 |
rs765044690 | snp | C/G/T | 4.94184e-05 | 0.00497063 | missense, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550789 | CTCATCTGGGACTTC[C/G/T]TAAATGATCCAGCTG | 8945 |
rs765073830 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491280 | TTTAGAAGTTGTTTT[A/G]GAATACAGATTTTAT | 8945 |
rs765074250 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424987 | ATTCCTCAGTGTCTG[-/T]TCCCTTCTTTATGTC | 8945 |
rs765087402 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487800 | ACAGAGGGAATGATG[A/G]AGGGAGCACCACAGC | 8945 |
rs765088656 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101385163 | TGATTCCTCCGCTGC[A/T]TTCCAGCCTGGGACA | 8945 |
rs765167040 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461038 | CTCTCGAGTAGCTGG[A/G]ATTACAGGCACCCAC | 8945 |
rs765198461 | snp | A/G | 7.63417e-05 | 0.00617778 | intron-variant | BTRC | GRCh38.p7 | 10:101521915 | ATTTGCTATGATGAT[A/G]AGAGAACTAGATCTC | 8945 |
rs765221268 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101424165 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 8945 |
rs765266861 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505605 | AACCTGGGCGACAGA[A/G]CGAGACTCCGTCTCA | 8945 |
rs765270704 | snp | A/C | | | intron-variant, synonymous-codon | BTRC | GRCh38.p7 | 10:101515926 | GTAGGAGTCACTCTC[A/C]GGGTGACTAGTGACC | 8945 |
rs765293641 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101477600 | ATCACAGGCATGAGC[C/T]ACTGTGCCCAGCTAT | 8945 |
rs765319781 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101368816 | TTGAGGCCAGGAGTT[A/C]GAGTCTAGCCTGGCT | 8945 |
rs765413451 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101478634 | CATCTCTACAAAAAA[C/T]ACAAAAAATTAGCTG | 8945 |
rs765415316 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101354044 | AGCCGATTCTCCTTG[G/T]CCCCTCAGCCTGCGC | 8945 |
rs765438758 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394407 | TATTCTTTTTGCAGC[A/G]TCCTGCTTGCCTGGC | 8945 |
rs765441907 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393735 | GTTGGAAAGAGTCTT[C/T]CCCTACACACTCCCC | 8945 |
rs765449781 | in-del | -/ACA | | | intron-variant | BTRC | GRCh38.p7 | 10:101420135 | GTAAGATTTCAGCTT[-/ACA]ACAACATCCTCAATT | 8945 |
rs765473927 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101500292 | ATACTGTACGCAATC[A/G]TAACATGATGGTGTT | 8945 |
rs765506483 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101368611 | TAGCCTCCTGAGTAA[A/C]TAGGACTACAGGCAT | 8945 |
rs765546390 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435744 | GGTCATAGAGTAAGT[A/G]TATTTTTAACTTTAA | 8945 |
rs765552550 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555617 | TCATTTCCAGAGAAG[A/G]TAAACCCCACTTACC | 8945 |
rs765554778 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537851 | CTTGGAATTTGTCTG[C/G]TATGTACCTTGAGGA | 8945 |
rs765571190 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554666 | CCCAGCCAATAAAGC[A/G]TCTGTGGCGATTGGT | 8945 |
rs765572954 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404855 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGT | 8945 |
rs765610646 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447429 | CCTTCATTGTATATA[A/G]GAGCAAAAGATGCAT | 8945 |
rs765611725 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101403371 | GGACACAAGGCAGCC[A/G]CCCTTGCATTCCTAA | 8945 |
rs765612187 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481907 | TGGTTCATTGCTTCA[C/G]ATTTGAGCCAAATAA | 8945 |
rs765617294 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409395 | ATGTTATAGCATTTA[C/T]TAGTAGTTTATTTTT | 8945 |
rs765618574 | snp | C/T | 1.77599e-05 | 0.00297987 | intron-variant | BTRC | GRCh38.p7 | 10:101414698 | TAGAAGACAGTGATA[C/T]TGATGATCCTTGCTC | 8945 |
rs765628562 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432751 | TTAGCCAAAAGAAGA[G/T]ACACATAGGGCAGAA | 8945 |
rs765635504 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101471153 | CTCTAGATTTGTTGT[G/T]TTATTTTTTGTTATT | 8945 |
rs765646565 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510371 | AAAATTTAGCCGAGC[A/G]TGGTGGTGGGTGCCT | 8945 |
rs765658556 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377817 | GTACTCTGAAGCCTA[C/T]CTACAAAGTTTTAAG | 8945 |
rs765699264 | in-del | -/TTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101408291 | TCCCATCTGTTCTTT[-/TTC]TTCTTTTTTTTTAAA | 8945 |
rs765708211 | snp | G/T | 0.000116538 | 0.00763251 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532317 | AATCTAATTGGAGAT[G/T]TGGAAGACATAGTTT | 8945 |
rs765722760 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101363429 | TGCTATAGAATTTAA[G/T]GGAGGGGAAGTTCGT | 8945 |
rs765746736 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101466192 | TTGTCTAATCCCTCT[C/T]CCATCCCCCATTTCC | 8945 |
rs765768695 | snp | A/G | 3.3134e-05 | 0.00407012 | synonymous-codon, intron-variant | BTRC | GRCh38.p7 | 10:101531300 | CAACTCTTTTTATAG[A/G]GCACTTTATCCTAAA | 8945 |
rs765776099 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362183 | CCAGGACAGTCTCGA[G/T]CTCCTCCTTGTGATT | 8945 |
rs765813943 | in-del | -/AGTC | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557203 | GTTATGGTGATGTGT[-/AGTC]AGTGTACCAATATGT | 8945 |
rs765860536 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440826 | TGCACTGGAAAAATG[A/G]TGTTGGTAATTCCTG | 8945 |
rs765874603 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101494963 | GTTTACAAGCATAGG[A/C]AGAGAACACAGGCTT | 8945 |
rs765879073 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404547 | CATTCAACCCAGTTG[A/G]CTTCAGTCTACAAGT | 8945 |
rs765882826 | in-del | -/TTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101395434 | TTATTTTCATTATTA[-/TTG]TCTAGGAGTTCCTCA | 8945 |
rs765904378 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428307 | ATGTCAGATTGACAG[A/G]GTGCTTGGATTTCAT | 8945 |
rs765913696 | in-del | -/ACAAAAAAAAAC | | | intron-variant | BTRC | GRCh38.p7 | 10:101522365 | TTAAAAAAAAAAAAA[-/ACAAAAAAAAAC]ACAAAAAAAAACAAA | 8945 |
rs765922924 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101475922 | TCCAAGTATTTTGCC[-/AT]ATATATATATATATA | 8945 |
rs765938566 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550771 | TCACATGATGACACA[A/G]TCCTCATCTGGGACT | 8945 |
rs765938669 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101439376 | CTGGTACGTTGATCC[A/G]ATGGTGTCCTGACCT | 8945 |
rs765961431 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101550507 | CAGGATGGTCTCGAT[A/C]TCCTGACCTCGTGAT | 8945 |
rs765974783 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101478942 | AGACTCCATCTGGGG[-/A]AAAAAAAAAAAAAAA | 8945 |
rs765994642 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101498986 | CAACAAGAGCGAGAC[C/T]CTGTCTCAAAAAAAA | 8945 |
rs766011206 | snp | C/T | 0.000165068 | 0.00908333 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430438 | CCAGGGACTGGCGCA[C/T]TCACAGCTTTCCAGG | 8945 |
rs766056705 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101542716 | AGCTGGGACCACAGG[C/T]GTGCGCCACCACGTC | 8945 |
rs766096485 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101502038 | TAAAAATGGTGCCCA[G/T]GTAGGGGACATATAA | 8945 |
rs766099677 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101491061 | AAGACTCTGTCTCAA[-/A]AAAAAAAAAAAACTC | 8945 |
rs766138313 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101413243 | CTGCCTCCTGTGTTC[A/G]GGCAATTCTCCTGCC | 8945 |
rs766143176 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465345 | ATTATTCAAAAATAG[C/T]GTTTTGCCATTGTTG | 8945 |
rs766176423 | snp | A/T | 1.65323e-05 | 0.00287505 | intron-variant | BTRC | GRCh38.p7 | 10:101532927 | ATCATCACATTGATC[A/T]AAAGGATCTTATTTG | 8945 |
rs766200123 | snp | C/T | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557478 | GGATGAGTGTGGGGT[C/T]CCTGGCTTACGCCTA | 8945 |
rs766210332 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101410093 | TATTTTCTGTTGTGG[G/T]TTTTCTTGTTTTAAT | 8945 |
rs766212284 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101401837 | GCGAGACCTCATCTC[-/A]AAAAAAAAAAAAAAA | 8945 |
rs766230417 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515019 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC | 8945 |
rs766236763 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101545329 | AAGAAGGCTAAACTT[A/T]TGTTGTCTACAAGAA | 8945 |
rs766245100 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399922 | TCATTTTGGATCCTT[C/G]TTGTGAATATGTAAC | 8945 |
rs766279183 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101439030 | CTGGCAGTAAGCTCT[-/C]CCTAGGTTTATGAAT | 8945 |
rs766280380 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517686 | TTCTTCAGAGTAGCA[A/G]AAGTTTCTATTGATT | 8945 |
rs766311141 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101475462 | GGAGAATCACTCGAA[C/T]CTGGGAGGTGCAGGT | 8945 |
rs766314086 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101489758 | GTTTCATCTGACTAG[C/T]GTTTCTGCCGGTATT | 8945 |
rs766324960 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543158 | GTTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 8945 |
rs766335302 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101513568 | CTTCTTTGATTCAGC[A/C]TGTTTTTGAGGTTCA | 8945 |
rs766336624 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | BTRC | GRCh38.p7 | 10:101534955 | ACTTAGAATGGGGGA[A/G]TTCATATGAAAATTT | 8945 |
rs766338224 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101519634 | TTGGATCCCTCTTTT[A/C]ATGACAGCAATACCT | 8945 |
rs766369845 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398594 | AGGCATGAGCAACTG[C/T]GCCCAGCTGAAATTT | 8945 |
rs766386128 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459176 | AGAATTTATTGGATA[C/T]AATTTAGCCTGATGA | 8945 |
rs766389668 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521821 | ACATGGGCACATAAA[C/T]TCGTATCTTAAACCT | 8945 |
rs766389775 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358564 | ATATTTGCTGTTTAA[C/T]AGACAACCTCAAAAC | 8945 |
rs766393714 | in-del | -/TCTGGATG | | | intron-variant | BTRC | GRCh38.p7 | 10:101485486 | GGTTTTAGTGCTGAT[-/TCTGGATG]TCTGGATGGCCCTTG | 8945 |
rs766423637 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101528117 | AATAACTCCTGAAAT[G/T]TCAGTTAAGGAGATT | 8945 |
rs766465119 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353445 | GAGCTCTAAACACTG[A/G]GAATTTCTTGAACCG | 8945 |
rs766484168 | in-del | -/TTTTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101511546 | TTTGTATTTTGGGTT[-/TTTTG]TTTTGTTTTGTTTTG | 8945 |
rs766496412 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101430707 | TGTTGGCTTTCAGAT[C/G]AAGTAGAAGTATGAT | 8945 |
rs766504014 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365123 | TTGGTGCCCAGGCTG[G/T]AATACAATGGCGCGA | 8945 |
rs766509248 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101382278 | ATGAGCCACCGCGTC[C/T]GGCCCCTAAGAATGT | 8945 |
rs766511424 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474308 | GTTAAGGTCAGGTGT[A/G]TTTTGGTTTTGCCCT | 8945 |
rs766519472 | snp | A/G | 5.07241e-05 | 0.00503582 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532298 | CCTTCTTCTCAGACA[A/G]TAGAATCTAATTGGA | 8945 |
rs766531402 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101410291 | TTATCGTGGTTTTGA[-/T]TTTTCATTTTCCCAA | 8945 |
rs766550631 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101367546 | CGTAACCATTATCTA[C/G]ATCAGGAATAGAACT | 8945 |
rs766555961 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423031 | GTATTGATATTGATT[C/T]TTCCTATCCATGAGT | 8945 |
rs766591606 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445380 | GTTAGAGCTTAGGGT[C/T]AGTATCTATAAAATA | 8945 |
rs766601633 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101368424 | TTATAGCAACGTAAA[C/T]GGACTAAGACACTTT | 8945 |
rs766610785 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101437269 | TAATAAAATGAATTA[C/T]TGTTTATTATGGAAT | 8945 |
rs766620388 | snp | A/G | 1.77562e-05 | 0.00297956 | intron-variant | BTRC | GRCh38.p7 | 10:101414606 | ATTCCAGAAAAAGGC[A/G]TTGATGTCATAGGAG | 8945 |
rs766669865 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101534320 | CTCCTGAGGGCTATC[A/G]TTGGAATGGGCACTA | 8945 |
rs766690594 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101498448 | GTGTGAGCCACCACA[C/T]CCGGCCTCCGAAGCT | 8945 |
rs766702083 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554393 | TTAAGAGAGATGGTC[A/G]GGAGAAAACACTGTT | 8945 |
rs766738267 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101506335 | TTAAATACAGTTGCT[A/C]AAGTTAGGCTTCAAC | 8945 |
rs766744730 | in-del | -/AC | | | intron-variant | BTRC | GRCh38.p7 | 10:101358044 | CCCCAAAACACACAA[-/AC]ACACACACACAAGCA | 8945 |
rs766757194 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417205 | AGTTTCTCTAGTAAT[C/T]TCAGTCAATGTCCTT | 8945 |
rs766763218 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101469394 | AGTCCTATATATAGC[C/T]CTACTCTGGAAACTC | 8945 |
rs766765786 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101430892 | TGCCCTCTTCAGAGT[A/G]TCTCCTGGTAATTAT | 8945 |
rs766823414 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537515 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 8945 |
rs766855280 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353852 | AACTACAATTCCCAT[C/T]AGCCGATTTCCTCTG | 8945 |
rs766897055 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423024 | GTCATTGGTATTGAT[A/G]TTGATTCTTCCTATC | 8945 |
rs766899777 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521132 | TAAAAATTAGCAGGA[C/T]ATGATAGTGTGTACC | 8945 |
rs766902645 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447068 | GGTTGGACTTTTTGC[A/G]GGTCAAGGCAGACCA | 8945 |
rs766910772 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371122 | ACCCATTAGACAAAC[-/T]TATCGATGTCTCCCT | 8945 |
rs766913971 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536688 | GTAAAAAAGAGAAAA[A/T]CTACGTCTTAATCCT | 8945 |
rs766925246 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495455 | ATCACCGTATTGCAT[C/T]TAACCGTGGGCAGCA | 8945 |
rs766941175 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101414857 | TTGTACTGCTGTACA[-/AT]ATGTTTGTGTTTTGA | 8945 |
rs766957632 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101486151 | TAACGCTCAGAGATC[A/G]GCAGGAGTCCTACTT | 8945 |
rs766969289 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510098 | GAGATTGCACCATTG[C/T]ACTCCAGCCTAGGTG | 8945 |
rs766972132 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101387530 | TACCTTCATGGGACT[-/TT]TTTTTTTTTTTTTTT | 8945 |
rs766977871 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554130 | GACTCAGCAGTCTCC[-/T]TGATTCCATGTAGAG | 8945 |
rs766993113 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453987 | GGGCCAGTTAAACTT[C/T]ATTTGCAAAAATATG | 8945 |
rs767006596 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101415405 | GGTCTTGAACTCCTG[G/T]ACTCAAGGGATCTGC | 8945 |
rs767022310 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101507050 | CATTTAATAAGATAA[C/T]CACGACATTTTAAAA | 8945 |
rs767043037 | in-del | -/T | 1.73757e-05 | 0.00294747 | intron-variant | BTRC | GRCh38.p7 | 10:101521886 | GTATGTCTACAAGTG[-/T]TTGTAAACCATTAAT | 8945 |
rs767074169 | snp | A/G | 1.65386e-05 | 0.00287559 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532335 | GAAGACATAGTTTAC[A/G]GAGAATTCACTGCCG | 8945 |
rs767077521 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101524398 | TTAGACCTGTGTATC[C/T]TTTACCTAATATTGA | 8945 |
rs767091762 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521814 | ATTACCAACATGGGC[A/G]CATAAACTCGTATCT | 8945 |
rs767096156 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101388726 | GAACTCCTGGCCTCA[A/G]GCAATCTGCCCACCT | 8945 |
rs767113139 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470695 | TTGTCTACCCCATGA[C/T]TGTGAAGATATTCTT | 8945 |
rs767114703 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401736 | CTGGCACTTTCTGAG[A/G]CTGAGTCGGGAGGAT | 8945 |
rs767151353 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550752 | ATTCCAGATTGTCAG[C/T]AGTTCACATGATGAC | 8945 |
rs767168545 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101478633 | CCATCTCTACAAAAA[A/C]TACAAAAAATTAGCT | 8945 |
rs767179873 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101440742 | AGAAAAAAAAAGGCA[A/G]CTATTTAGCTTAGCC | 8945 |
rs767196374 | in-del | -/AAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101526771 | GTCACCTTTGTAATC[-/AAA]AATTATTTTTAAGCC | 8945 |
rs767210965 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101530921 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 8945 |
rs767212790 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101387793 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8945 |
rs767240337 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369699 | CACACAGGTGCACAT[C/T]GCACATTTACGTTGT | 8945 |
rs767271378 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516322 | GTTTTATAGATGAGA[A/G]AATTAGACTCAGAAG | 8945 |
rs767292660 | in-del | -/AAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101357856 | TTAACTTTTAAAAAC[-/AAAT]AAATGATATTGAAAG | 8945 |
rs767296556 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101548081 | AATAAATGTAAAAGA[C/T]TGGTAATATCAATTT | 8945 |
rs767309687 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101517053 | AAATCTTCACATTTC[A/C]TGAGTTTTCATTTCT | 8945 |
rs767340983 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425198 | CTTTATCCAGTCTTC[C/T]GTTGATGGGTACCTG | 8945 |
rs767343307 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441832 | ATAGCAGTCAGCCGA[C/G]ATCACACCCACTGCA | 8945 |
rs767345918 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101403149 | GTAGCTTCCTGAGGT[A/G]TCTTCTCTGGGGACG | 8945 |
rs767362109 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463656 | ATAACCCTGTAAAGT[G/T]TTTAGATATGATGTG | 8945 |
rs767433007 | snp | G/T | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534664 | TATCACTTCCAGAGT[G/T]TGGGATGTAAATACA | 8945 |
rs767435335 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557196 | TGATTATGTTATGGT[A/G]ATGTGTAGTCAGTGT | 8945 |
rs767451764 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556133 | AAAAGTCTGGCCCTC[A/G]TAACTTGTTTCCGAA | 8945 |
rs767465239 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398427 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8945 |
rs767494610 | in-del | -/AAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101508915 | CAAGACTCCATCTTA[-/AAAA]AAAAAAAAAAAAAAA | 8945 |
rs767527341 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472927 | CTGTGATGGGCCTAT[A/G]TGTGTTGTTTTCTTT | 8945 |
rs767532378 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371281 | GCAGACTCCGCCAAG[C/T]AATTCTCCTGCCTCA | 8945 |
rs767532729 | snp | A/C | | | intron-variant, synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354238 | TTTATGGTGAGGAGA[A/C]GGTGGAGGCCGGGGA | 8945 |
rs767532898 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101376987 | ATGTACACAGTTTTA[A/G]GAATTCTAATATGTG | 8945 |
rs767539055 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101542885 | TTTTTTGTTGTTGTC[A/G]TTGTTTTTGAGACGG | 8945 |
rs767556140 | snp | A/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514784 | TTGGCATCTTTCTTG[A/T]AAGTCAGTTGGCTGT | 8945 |
rs767563456 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101503434 | AACTTTACTAACTTG[C/T]GTGAATCTGAGCAAG | 8945 |
rs767571204 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101455467 | AGATATAAAGAGATA[C/T]AAAGAATTAAGTGCC | 8945 |
rs767583472 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379457 | ACCTGTTCTTTTTCA[A/G]TGTGTCTTTAAAATG | 8945 |
rs767593309 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465286 | AGTTCAGTTATCTTC[C/T]AGCAATTTAACATTG | 8945 |
rs767595745 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101529288 | AATTCAGATACTTTA[C/G]CAAGACATGGTAAAT | 8945 |
rs767601634 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463172 | TGCCTCAGCCTCCTG[C/T]GTAACTGGGACTACA | 8945 |
rs767624638 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101457513 | TTCAATATTTTAGGA[C/T]CTCAGTTGACTGTAG | 8945 |
rs767651102 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419995 | ATGTGTTTGTTGCTA[A/T]TAGGTTGCTCCTAGG | 8945 |
rs767654045 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488325 | CTGTTTTGTTTTTCT[A/G]TTACCTGTGCTATTG | 8945 |
rs767663708 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526599 | AGCCTGGCCAACGTG[C/G]CGAAACCCCAACTCT | 8945 |
rs767676166 | in-del | -/TTTTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101381963 | TATCCTAAGAATGTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 8945 |
rs767683874 | snp | A/G | 3.31741e-05 | 0.00407259 | synonymous-codon, intron-variant | BTRC | GRCh38.p7 | 10:101531249 | TAGGGGACAGTATTT[A/G]TTCAAAAACAAACCT | 8945 |
rs767688769 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404741 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 8945 |
rs767720265 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527962 | ATAAAAATGGAGTTA[C/T]ATGGTATTCGGGGTC | 8945 |
rs767729747 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396805 | TCTATCTCCAAAAGA[-/T]TTTTTTTTTTTTTTT | 8945 |
rs767737099 | snp | C/T | 1.7063e-05 | 0.00292082 | intron-variant | BTRC | GRCh38.p7 | 10:101535478 | ACACTATCAGGTGAG[C/T]AGCAAGTGCCTTGTA | 8945 |
rs767756394 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450684 | CTTTGAAATAACTGT[C/T]AGTGCTGCCCCAAAA | 8945 |
rs767760113 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474072 | TTAGAGCTATAATAT[C/G]TGCTAATTTCTACAA | 8945 |
rs767784372 | in-del | -/TAAAA | 3.31066e-05 | 0.00406844 | intron-variant | BTRC | GRCh38.p7 | 10:101462079 | AAATTCAGCCTTACT[-/TAAAA]TAAAAAGCTACCAAC | 8945 |
rs767789262 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511893 | TAACCTCAAGTGATC[G/T]GTCCGCCTCAGCCTC | 8945 |
rs767795758 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436728 | TAATTTTAGGAAAAT[C/G]TTGAGCTAAGTGAAA | 8945 |
rs767808064 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544925 | TGGGCATGGTGGCAC[A/G]TGCCCAGTGCAACAA | 8945 |
rs767821648 | in-del | -/CTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101397496 | AGACAGATCTCTGTC[-/CTTT]CTAATTGTGTTTCAA | 8945 |
rs767844098 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373713 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 8945 |
rs767855187 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505636 | AAAAAATAAAAAAAA[A/T]AAAATAATAATAAAA | 8945 |
rs767870235 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101504786 | ATAACCTATAATTCT[C/G]TGTCCTCCAGGATCA | 8945 |
rs767884621 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483728 | CCTGTGTTTCATGAG[A/G]TTTGTGTTTGGAGCA | 8945 |
rs767899552 | in-del | -/TTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101544388 | GACAAATACTTTCAC[-/TTG]TTGTTTACTTGGGAA | 8945 |
rs767912034 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551759 | CTGTCCTCAGCTTCT[C/G]TTTCTCTCACAGAGG | 8945 |
rs767916664 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381003 | ACATAGAAAGGGTAC[A/G]GTAAAAATACAGTGT | 8945 |
rs767944462 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536400 | AAAGGAAATAAATTA[C/T]ATTGAAAGCAGTACA | 8945 |
rs767947341 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498215 | CTGGAGTGCGGTGGC[A/G]TGATCTCAGCTCACT | 8945 |
rs767982710 | in-del | -/CTCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101551478 | ACTCAAGTCTCCAAC[-/CTCT]CTCTCAGGCAGGGGA | 8945 |
rs768007201 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549295 | AAAAAGCCAGGTGTG[A/G]TGGCATGAGTCTATA | 8945 |
rs768026178 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364843 | TTTTTTTGTATCCCC[A/G]GAGCGAGTGCACCGT | 8945 |
rs768036562 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101535156 | GAGTAAATCAATCTG[A/T]GGAATTCTCATGTGG | 8945 |
rs768059400 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101513129 | TTGCTGAATTTACTT[C/T]AGATAATTGTAGAAA | 8945 |
rs768069116 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392286 | CCCAGTGAAAACATT[C/G]TTAAATTCTGAGCAC | 8945 |
rs768071719 | snp | A/G | 1.65021e-05 | 0.00287241 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101462003 | CAGAGAGAGAAGACT[A/G]TAATAATGGCGAACC | 8945 |
rs768085300 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521699 | CGGAAACTCTCAGCA[A/G]GCTATGAAAAGGAAA | 8945 |
rs768089065 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101461803 | ATTTATTTATATACA[C/T]GGGCATATGTTTTCT | 8945 |
rs768107765 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555215 | GTCAGACATTTAAAA[A/G]GCATGGGTTTCGAGC | 8945 |
rs768108827 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101498865 | GGGTGTAGTGGTGCG[C/T]GCCTGTAATCCCAGC | 8945 |
rs768117955 | in-del | -/ATATATA | | | intron-variant | BTRC | GRCh38.p7 | 10:101366780 | GTTATATATATATAT[-/ATATATA]TATTTTTACATTTAT | 8945 |
rs768118598 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101539116 | CCCTTAGTTCTGCAG[C/T]CTATTCATGAGGTAG | 8945 |
rs768130606 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101370111 | TGTATGGACATATCC[C/T]TTATCCTGTTTTTTT | 8945 |
rs768149725 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428744 | ATTAAGCGTAGTCCT[A/G]TGGGTGGTAAATAAA | 8945 |
rs768179036 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101361628 | ACAGTTTCAACTAGT[A/G]TTCCACAATATTTCT | 8945 |
rs768185999 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394101 | GATATTTCCATCTCA[A/G]TTCTATTTAGAAGAT | 8945 |
rs768189890 | snp | G/T | 3.31923e-05 | 0.0040737 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535355 | ATTTTCTTTTTCAGG[G/T]ATGGAACACAAGTAC | 8945 |
rs768212390 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537423 | ATCCCAGCTACTTAG[A/G]AGGCTGAGGCAGGAG | 8945 |
rs768220872 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501206 | AAAAAAAAAAGAGGT[A/G]TATGCTTAAACGCCA | 8945 |
rs768228515 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534784 | TCGTTCCATTGCTGT[A/G]TGGGATATGGCCTCC | 8945 |
rs768266768 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510227 | AAAGTCATTATTTTT[A/G]GCCGGGTGCAGTGGC | 8945 |
rs768284128 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379056 | GACTATAAATTTCAC[A/G]TAATTTAAAAACAAT | 8945 |
rs768349249 | snp | A/C | 1.64779e-05 | 0.00287031 | intron-variant | BTRC | GRCh38.p7 | 10:101534917 | ACTATAAAGGTAATA[A/C]GGCATTTTTCAGTAA | 8945 |
rs768350127 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525042 | GAACTATTTAAGTCT[C/G]TAGAAAACCTCTGAT | 8945 |
rs768383020 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487538 | CAGTGAGCTGTGTGC[A/G]TTATTTTCTCCTGAT | 8945 |
rs768412071 | snp | A/C | 1.6477e-05 | 0.00287024 | intron-variant | BTRC | GRCh38.p7 | 10:101538277 | CTAACATTTTTGTCC[A/C]CTTTTTGATCTTTAG | 8945 |
rs768418514 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389790 | CCACCATGCCTGGCT[A/G]ATTTTTAAATTTTTT | 8945 |
rs768435114 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457128 | AACAGTTATAACTAT[A/G]CTGTAATAAAAGTTA | 8945 |
rs768440574 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101426556 | AAATTCTTTGTTGTT[A/G]GTAGTTTTGATGGAG | 8945 |
rs768468776 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403039 | TAACCTCTTTAAAAG[C/T]AGGGACTCATTTAGC | 8945 |
rs768503807 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362968 | ATGTGTGTAGGTTAT[A/G]TGCCGTTTAAGGCAC | 8945 |
rs768521078 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424608 | CAGCTTTCGTATAGT[A/G]AATGCTGAGGCTAGC | 8945 |
rs768529193 | snp | A/G | 0.0001065 | 0.00729648 | intron-variant | BTRC | GRCh38.p7 | 10:101414655 | TTAATTGCTCCCAAA[A/G]ACCTTCCAGTGCCAT | 8945 |
rs768542650 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471985 | TGACGTATCTTCATC[A/G]TTCTGAGTATTTCCA | 8945 |
rs768553963 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101390769 | GTTTGTCTTAAAAAA[-/G]AAAGAAAGAAAGAAA | 8945 |
rs768556077 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101500706 | TAAAACCTTAAAGCT[C/T]TTAAGATTTTAAATT | 8945 |
rs768570490 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465321 | TAACTAATATTATAG[G/T]TGACATATATTATTC | 8945 |
rs768574443 | in-del | -/TTTTATTTTA | | | intron-variant | BTRC | GRCh38.p7 | 10:101388331 | CCACACCCAGCTAAT[-/TTTTATTTTA]TTTTATTTTATTTTA | 8945 |
rs768633816 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383057 | GGCCTTCCCTGGAGA[-/T]TTTTTTTTTTTTTTT | 8945 |
rs768642809 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101393893 | CTCCAGATTTCATAT[A/G]TTGTGGAAAAGCAGT | 8945 |
rs768653797 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551288 | AGCCAAGTAAACAGT[C/T]TGATGTCTAATGTGT | 8945 |
rs768703917 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387679 | TTACAGGTGCCCACC[A/T]CCACACCCGGCTGAT | 8945 |
rs768704689 | snp | C/T | 1.68235e-05 | 0.00290026 | intron-variant | BTRC | GRCh38.p7 | 10:101479342 | CAATATTTTAAAAAC[C/T]TGTTTCCAACAAATT | 8945 |
rs768725324 | snp | C/T | 0.000105949 | 0.00727759 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354187 | TCGGCGATTATGGAC[C/T]CGGCCGAGGCGGTGC | 8945 |
rs768742029 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549832 | TCTACATCTTCATCA[C/G]GGTGGTAACTGCCAG | 8945 |
rs768752654 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370867 | TTACAGGTGTGCACC[A/G]CTTCACTGGGCCAAG | 8945 |
rs768759222 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427710 | TTTTTTAAATTTTTT[A/G]TAGAGATGGGGTCTC | 8945 |
rs768786854 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483317 | AAACTAAAAATGGCC[A/G]GGCACGGTGGCTCAC | 8945 |
rs768803098 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547195 | ATTTGAGGAGCATCT[C/G]TATTTTAAACTATTT | 8945 |
rs768806258 | snp | A/C | 1.65165e-05 | 0.00287367 | intron-variant | BTRC | GRCh38.p7 | 10:101536670 | TGAGTGTGCTAACAG[A/C]GTGTAAAAAAGAGAA | 8945 |
rs768824644 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438240 | GACCATCCTGGCTAA[G/T]GCGGTGAAACCCCGT | 8945 |
rs768833163 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490082 | AAGATTATCATAATT[C/G]TAAGTTTTCTCTCCC | 8945 |
rs768836514 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101503014 | TTATTTTAATCTTAA[A/C]ATTAGCCCTTCTAGC | 8945 |
rs768842527 | in-del | -/TTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101383060 | CCTTCCCTGGAGATT[-/TTTTTT]TTTTTTTTTTTTTTC | 8945 |
rs768847150 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533982 | ATGATATTCTATAAA[A/G]GGGGGCTAAACTGGA | 8945 |
rs768852343 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464871 | TTGGCTTGTGTCTGT[C/T]TATTGTGGTGGTCAC | 8945 |
rs768890358 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436504 | TAGCTGGGTGTGGTG[A/G]TACTCACCTGTCCCA | 8945 |
rs768907407 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481944 | GGTCAATGTCAAATA[A/G]AAACACATAGCTGAA | 8945 |
rs768912107 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356764 | ACAGTCTTATGAATC[G/T]GAGTAAGTCACAACT | 8945 |
rs768916186 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372401 | CTGGGATTACAGGCA[C/T]ACACCACCACGCCCG | 8945 |
rs768927279 | in-del | -/T/TTTTTTTTTTTTTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101482393 | TTGTTTGTTTGTTTC[-/T/TTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8945 |
rs768936755 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450554 | TAAGCTACATGTTCC[A/T]GTATAACAGGCACCA | 8945 |
rs768990158 | snp | C/T | 1.65594e-05 | 0.0028774 | intron-variant | BTRC | GRCh38.p7 | 10:101479473 | GTAAGTAATATTGCT[C/T]ATCAATGTATATTAC | 8945 |
rs768994008 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412348 | TGTGCAGCAGCCTGG[A/G]CAGTACCTTCGGGTA | 8945 |
rs769037760 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533116 | TGAAATATCAGCTCT[C/G]CTCTGTTCTTTGTCA | 8945 |
rs769067353 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101489028 | ATGCCTCTACTTAAA[A/C]CTCATTGTACAAAAG | 8945 |
rs769098517 | snp | A/T | 6.61059e-05 | 0.00574879 | intron-variant | BTRC | GRCh38.p7 | 10:101461967 | ACTGAATTAAAGCTT[A/T]CTTTCTTTCACAGAA | 8945 |
rs769103978 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101423877 | GTGGCATTCACAGAA[C/G]CCTATTCCTGGTGAT | 8945 |
rs769104137 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101530497 | GACACAGTAAAAGGG[-/A]AAAAAAAAAAAACCT | 8945 |
rs769109761 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527767 | TCTTTCTCTGTCTCT[C/G]TCTCTCTCTCTCTCT | 8945 |
rs769119728 | in-del | -/TAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101381238 | ATCTTATTAGGTGTG[-/TAT]TATTATTATCATCCT | 8945 |
rs769129159 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414341 | GTAGCCAATGTAACG[C/T]CATATAATGCAAGGC | 8945 |
rs769129771 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101498798 | GAGTTCGAGACCAGC[C/T]TGACCAACATGGTGA | 8945 |
rs769162721 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380875 | TAGACAAATCTAGAT[A/G]GTATACCTTACTATA | 8945 |
rs769169383 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428807 | CATAGATCTCCTTTG[A/G]ATTTATTTGCAGCCC | 8945 |
rs769176964 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399247 | GGCGTGAGCCATCAT[C/G]CCTATCCAGAAACCT | 8945 |
rs769192452 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366695 | TTATAGGTGGGTAGA[C/T]AGATATAATTTGAGT | 8945 |
rs769197843 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544763 | TATTTTTGCTGGCTA[A/G]ATAATTCTATATAGG | 8945 |
rs769201079 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504614 | TTCCTCTTCTACCCT[C/T]TTCTCTAGCCCTAGC | 8945 |
rs769212841 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438000 | ATCTGTACCCAGAGC[A/G]TGCATGGAATTCTGT | 8945 |
rs769215394 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534771 | CCTGCTCCAAAGATC[A/G]TTCCATTGCTGTATG | 8945 |
rs769229807 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476827 | TTACTGTTGGTTTTG[A/T]GTGTCTTAAGATTTT | 8945 |
rs769236452 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101528850 | CTAACCAAAAATAGT[A/G]AGTAAATACAGTTTT | 8945 |
rs769259814 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533042 | GATGAGAGAGTGATC[A/G]TAACAGGATCATCGG | 8945 |
rs769261244 | in-del | -/T | 1.69602e-05 | 0.00291201 | intron-variant | BTRC | GRCh38.p7 | 10:101430501 | ATTAGTGTATGTGTC[-/T]TAATTCATTAGTATG | 8945 |
rs769270536 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101375429 | ACAGCCTGCAGAACC[A/G]TGAGCCAATGAAACC | 8945 |
rs769273764 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400532 | GAAGATGATCCATAA[A/G]TCTAATGCTAAGGAT | 8945 |
rs769306774 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506062 | GGGACTACCGGTGCC[A/G]GCCACCATGCACTGC | 8945 |
rs769347756 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352576 | CTGCACACGGTTATA[C/T]GCTTACCATTTGTTG | 8945 |
rs769349586 | in-del | -/AACCCCCCCGTTC | 1.64761e-05 | 0.00287015 | frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550814 | CAGCTGCCCAAGCTG[-/AACCCCCCCGTTC]CCCTTCTCGAACATA | 8945 |
rs769359871 | snp | A/C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537019 | AGGGCAGTATTTGGG[A/C/G]ACTTAGTGTGGTAAG | 8945 |
rs769363226 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474304 | ATTTGTTAAGGTCAG[C/G]TGTATTTTGGTTTTG | 8945 |
rs769363814 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432065 | GTTATAAACATTATT[G/T]CTATTATTGGAGAGT | 8945 |
rs769377790 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101548088 | TAAAAGATTGGTAAT[-/A]ATCAATTTTTGGTGA | 8945 |
rs769388588 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459742 | TTGTGTTTTCATTCT[G/T]TAGACATTTTCATAA | 8945 |
rs769393328 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393199 | TGTGCCCAGGGAGTC[A/T]TGGCAGCTCTGAGCC | 8945 |
rs769401489 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101455044 | TTAACCTGGCAATAA[C/T]ATTCAATCCAAGAAA | 8945 |
rs769414399 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445610 | CGGTCTGTCTATTGG[G/T]CTCTTTTTAAATCAG | 8945 |
rs769452848 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524032 | CCTAATAAAAATATA[C/G]CAGCTCATAGCCTCC | 8945 |
rs769468072 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484525 | TGCAGACGTTTGCAC[C/T]TCCTCTGGGTCTGTG | 8945 |
rs769470291 | snp | A/C | 0.000108056 | 0.00734956 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354165 | GCGGAGAGCGGACCC[A/C]GTGGCCTCGGCGATT | 8945 |
rs769519801 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101499703 | ATGTCTATTCTGATA[C/T]CAGCCCACTCTTCCA | 8945 |
rs769520598 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101431900 | ACTATGAGATACAAT[A/G]TAGTAAAGCATGCAG | 8945 |
rs769534537 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369616 | TAGAAGTCCAGATCT[C/G]GGTGTTAAGCGTGCT | 8945 |
rs769536004 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101480396 | AGCTGGGTGGCTTAT[-/A]AAACAAAACTAATTT | 8945 |
rs769542579 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538568 | TGCTTTAGAGACTAT[A/G]TATGGAGAGAAATGT | 8945 |
rs769555233 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547576 | AAACTCCGGACCTCA[G/T]GATCCACCTGCCTCA | 8945 |
rs769574225 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101446725 | GACTTGCTGCCCACA[A/G]AATATCCCTGACTAG | 8945 |
rs769575698 | in-del | -/AC | | | intron-variant | BTRC | GRCh38.p7 | 10:101393713 | GAGAGTAGTGGAAAA[-/AC]ACGAGGTTGGAAAGA | 8945 |
rs769597393 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416534 | TCTTCCATGGTGTCA[A/G]TTGAAAGCCTGAGTT | 8945 |
rs769630257 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468909 | TTGTTAGATAATCCT[A/G]TGTCATTGAATCCAT | 8945 |
rs769646472 | in-del | -/AAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101404998 | GCTAGAATCCATCTT[-/AAA]AAAAAAAAAAAAAAA | 8945 |
rs769654621 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101357440 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 8945 |
rs769666424 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449456 | GTCCTTATTAGTGGA[A/G]GCAAATGTTTGCCTC | 8945 |
rs769676619 | snp | A/C | 6.82967e-05 | 0.00584326 | intron-variant | BTRC | GRCh38.p7 | 10:101531189 | ATATATATGTATTTA[A/C]ATATATAATGTCATG | 8945 |
rs769679598 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456945 | ATATTTTAATATACT[A/G]TAGTCCCCACTTATT | 8945 |
rs769683253 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485576 | AAATCTAAAACTTTC[A/G]GTAGTTCTTTTGAAC | 8945 |
rs769690162 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101417592 | CTTTATATTTTTCCA[A/G]TTAAAACGAAGTAGT | 8945 |
rs769690972 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101433184 | ATGGATCTCTTTGGG[A/C]ATCTGATGAGAACTA | 8945 |
rs769697579 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101521928 | ATAAGAGAACTAGAT[C/G]TCCAGCTATATATCT | 8945 |
rs769702933 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507803 | GGTATGTCTGTGCCT[A/G]TTTCAATCATTTCTT | 8945 |
rs769738800 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101359836 | AACTCCCAACCTCAG[A/G]TGATCTGCCCGCCTT | 8945 |
rs769783805 | snp | A/G/T | 9.93648e-05 | 0.00704795 | intron-variant | BTRC | GRCh38.p7 | 10:101536509 | CTTAGAAAAGAATAC[A/G/T]TGAAAATTCACCTGA | 8945 |
rs769838165 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | BTRC | GRCh38.p7 | 10:101479318 | TGAAAACAGGATATG[A/G]CAGTATTTCAATATT | 8945 |
rs769841252 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401137 | TGAGATTTGACTTGA[A/G]TTTAATACAATGAAG | 8945 |
rs769847885 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533011 | CCATACAGGTTCAGT[C/T]CTCTGTCTCCAGTAT | 8945 |
rs769849502 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101479758 | TAATGTACAATTGTT[C/T]TGATAAGTTTATGGT | 8945 |
rs769894775 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441584 | TTGTTGGTTCTACTA[C/G]AAAGTTTTTTCTTGG | 8945 |
rs769905442 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510749 | GGTAGTAAAGTATTA[C/T]ACTAAAATAAATGTA | 8945 |
rs769906607 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536634 | GATAACAAGAGGATA[A/G]TCAGTGGGGCCTATG | 8945 |
rs769908228 | snp | G/T | 4.94931e-05 | 0.00497434 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526072 | GATGCCAAATCACTA[G/T]GTGCTGCTGAACTTG | 8945 |
rs769920096 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530536 | TGTGCTAGTTCAAAG[A/G]TAATAGTTACCATTA | 8945 |
rs769952513 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533651 | GAACCTCTGTTAGGA[A/G]TTTTGCCGTAAGCTA | 8945 |
rs769966309 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461445 | GCTGCTGTTTGAGGT[A/G]ACAGTGCCAAGGAAT | 8945 |
rs769976350 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101390908 | AGATTAATTTTATAC[-/T]TTTTTAAGACTTGTA | 8945 |
rs769987091 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370714 | GCTGGGACTACAGGC[A/G]TGTACCACCAAACAT | 8945 |
rs769993697 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488001 | ATAATCTATAGACTG[C/T]AATTCTATCAGGAGT | 8945 |
rs770025776 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360648 | AGTGCTGGGATTATA[A/G]GCATTAGCTACCGCG | 8945 |
rs770028509 | in-del | -/AG | | | intron-variant | BTRC | GRCh38.p7 | 10:101412560 | GCTTGTTTTTACTTT[-/AG]AGAGTTTAATTTTAT | 8945 |
rs770040014 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369339 | TCCTCCCACCTGGGC[C/T]TCCCAAAGTGCTGAG | 8945 |
rs770040377 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101389458 | GATCTAAAATGTTCT[A/C]ATATCTTCCTTTTGG | 8945 |
rs770043784 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101355423 | TTTTTGCTGTGCTTA[G/T]CTTTGGCAAACTCGT | 8945 |
rs770052150 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544152 | CTGACCTCGTGATCC[A/G]CCCGCCTCAGGTTCC | 8945 |
rs770056166 | in-del | -/AAAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101390769 | TTTGTCTTAAAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 8945 |
rs770058760 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101494150 | CTAGTTTGAGCTGCT[C/G]TTAGAATGAATGTGG | 8945 |
rs770080395 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463326 | TGGGATTACAGGCAT[A/G]AGCCACTGTTCCCGA | 8945 |
rs770081164 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410859 | ACATTCCTATCCTTT[A/G]TGTTATTATTGTCAT | 8945 |
rs770082087 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101395634 | ATGAACTTAAAATGA[A/T]CATGCTATGAAAGAT | 8945 |
rs770098651 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464576 | AAATGATTTTTCTAA[C/T]ATCTGTCATTCAGTG | 8945 |
rs770122853 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501481 | TGTTGCCTCACTTTT[A/G]CTTTCAGGCTACATT | 8945 |
rs770128576 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450304 | TCCCCATATTTATTG[C/T]TACAAATTTGTCTTT | 8945 |
rs770181303 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101549550 | AACCCCGTCTCTACT[-/A]AAAAATACAAAAAAT | 8945 |
rs770209271 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514159 | CTAAGAGTTCTTTAT[A/G]GATGCTGGATACAAG | 8945 |
rs770223632 | snp | C/T | 1.65861e-05 | 0.00287972 | intron-variant | BTRC | GRCh38.p7 | 10:101532903 | ACCAACAAGTCTCCA[C/T]AGCACCCCATCATCA | 8945 |
rs770274739 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380638 | AAGTACATACATGTA[C/T]ATCCTTTTTGAAATG | 8945 |
rs770280873 | snp | A/T | 8.40852e-05 | 0.00648348 | intron-variant | BTRC | GRCh38.p7 | 10:101521876 | GCTCTGCCAGGTATG[A/T]CTACAAGTGTTTGTA | 8945 |
rs770282911 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101419603 | CTTGTTTCATCAAAG[C/T]GTGCAAACCAAGAAG | 8945 |
rs770289891 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101435036 | CAGGTTCAGCACACA[C/T]AGGTGCTTGATAATA | 8945 |
rs770297853 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101424812 | ATCTTGTTTTTTCAA[-/C]TTTTATTTTAAAATT | 8945 |
rs770313073 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421124 | TCTTCTAGTCATTCA[A/G]GTTTGAAATGTTGAA | 8945 |
rs770366569 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488932 | ATAACTAATGTAGAT[G/T]ATATGTATCATAATA | 8945 |
rs770376449 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101382061 | GATCTCAGCTCACTG[C/G]AACCTTCGCCTCCCA | 8945 |
rs770380997 | snp | C/T | 9.90246e-05 | 0.0070358 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550707 | TCTTTAGGAGCATTC[C/T]GGAAGAGTTTTTCGA | 8945 |
rs770381892 | snp | A/G | 0.000110223 | 0.0074229 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354149 | CAAAGGGGCGGCCCC[A/G]GCGGAGAGCGGACCC | 8945 |
rs770414808 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405691 | TATATGTTCTGTCCA[-/T]TTCTTAGTGGTTGCC | 8945 |
rs770457195 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378190 | CTATCTCTTCTCCTT[C/T]GTAGATCATCCCAAG | 8945 |
rs770459351 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101542102 | TCTTTAATAAATACA[A/G]CACTCTTCAGATTTA | 8945 |
rs770469762 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456602 | CTTTTTTATTCGCCC[A/G]GTTTGGTTGTGGAAA | 8945 |
rs770470808 | snp | G/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352774 | CAGCCTGGAGTGCAG[G/T]AGCGTGATCTCGGCT | 8945 |
rs770485751 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398086 | CAGGTTTTTGTGGTA[A/T]TGGCATTGGCATCTC | 8945 |
rs770499113 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101444306 | AGATTTTCAATCCTT[A/G]TTGTCTTCAGAACTG | 8945 |
rs770503499 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364266 | TAATGTAATACAGCA[C/G]ATTTCTTCTCTTCAT | 8945 |
rs770518438 | snp | C/T | | | stop-gained, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532415 | ATAGTAAGCGGCCTT[C/T]GAGACAACACAATCA | 8945 |
rs770543881 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405648 | TACCTGCTAGTATTT[A/G]ATTTTTTGAGTCTTC | 8945 |
rs770546842 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407393 | CATAATGTATTTTAT[G/T]TAACACACCGTAATT | 8945 |
rs770557078 | snp | A/G | 3.30606e-05 | 0.00406561 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526050 | TGAGAACATTCTGTC[A/G]TACCTGGATGCCAAA | 8945 |
rs770565465 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458660 | CTATTTCATGGCCTT[A/G]ACATTTCTTAGGTAC | 8945 |
rs770569749 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101530691 | TACTCCGATGTTCTA[A/C]ACTGGAAATAATCAT | 8945 |
rs770577460 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101513893 | TAAACGTGACTGCCA[A/G]CAATGTGTGAGAGAC | 8945 |
rs770594353 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101446789 | TATGAGCAAAACTTT[-/A]AAAAAAAATTAACCA | 8945 |
rs770601454 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537057 | ATTTTGATTTCTTGG[A/G]TTTTTTATCTCTTTG | 8945 |
rs770603527 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367101 | TTCGAGCTAGAGTCT[C/T]GCTCTGTCGCCCAGG | 8945 |
rs770605563 | in-del | -/C | 3.31299e-05 | 0.00406987 | intron-variant | BTRC | GRCh38.p7 | 10:101536689 | TAAAAAAGAGAAAAT[-/C]TACGTCTTAATCCTT | 8945 |
rs770607689 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446616 | ATTTTGTTGAGAGGC[A/T]CTTTGCTTTCTATAT | 8945 |
rs770618473 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473708 | ACTCCTGACCTCAGG[C/T]GATCTGCCCGCCTCG | 8945 |
rs770626229 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396919 | GCAATTCTCCTGCCT[C/T]AGCCTCCAAAGTAAC | 8945 |
rs770643834 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484145 | GTATTTTAGTTGTTA[C/T]TGGTTGTTGTCACTG | 8945 |
rs770662492 | snp | A/G | 7.33326e-05 | 0.00605483 | intron-variant | BTRC | GRCh38.p7 | 10:101521907 | AACCATTAATTTGCT[A/G]TGATGATAAGAGAAC | 8945 |
rs770720347 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101476296 | ATGTGGGATCCTAGA[A/T]TAGATGCTGAACAGA | 8945 |
rs770723042 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459577 | TAAAAGAACATACCA[A/T]TGTTTATGGGTTTCC | 8945 |
rs770734609 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101430261 | GCAACTGGAATATTG[C/T]GTTCAGCCAAGCCTT | 8945 |
rs770738766 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101458044 | ATGTTCCATCCCCCC[-/T]AAATGTTTCAGTGCG | 8945 |
rs770745722 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101548569 | CCAGCCTGGGCAACA[C/G]GGTGGAATCCTGTCT | 8945 |
rs770770324 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101498708 | GAAAATAATAATAGC[A/C]GGCCAGCCGTGGTGG | 8945 |
rs770789945 | snp | C/G | 1.65712e-05 | 0.00287843 | intron-variant | BTRC | GRCh38.p7 | 10:101536503 | TCCAGGCTTAGAAAA[C/G]AATACGTGAAAATTC | 8945 |
rs770820290 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535389 | TGAATTTGTAAGGAC[C/T]TTAAATGGACACAAA | 8945 |
rs770820798 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101536243 | TTAGCTTGGTCATTT[C/T]CTTCTCAGGCAACTG | 8945 |
rs770821253 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520431 | TTTTGTTCACTGTTA[A/T]ATTCCTAGTACCAAG | 8945 |
rs770865551 | in-del | -/TAATG | 1.78182e-05 | 0.00298476 | intron-variant | BTRC | GRCh38.p7 | 10:101414729 | TCTGTGGGCCTAGGC[-/TAATG]TAATGTGTGTGTTCA | 8945 |
rs770884176 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101373374 | CTTGAGCTAGGGCAG[C/T]AGGTATGGAAAAGGA | 8945 |
rs770930256 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524042 | ATATACCAGCTCATA[A/G]CCTCCCAACTATTAA | 8945 |
rs770934250 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101380420 | TAATGTCAAAAATGC[-/A]AACTTGGGGAGGGCA | 8945 |
rs770975751 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545063 | TCAAAAAAAAAAAAA[-/G]GAAAAAAAGCTAGAT | 8945 |
rs771010534 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430387 | GGCTGCTCCAGCCTG[A/G]CGGACAGCATGCCTT | 8945 |
rs771020158 | in-del | -/CACAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101467210 | TAAAAAAAAAAAAAA[-/CACAG]AATTTGCTTCCTTTA | 8945 |
rs771033278 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454778 | ATAGAGCAAGACCCT[G/T]TCTTTAAAAAACAAT | 8945 |
rs771048836 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538532 | ATAAAATATGTTTAT[A/G]TAATTCCTTTCATCC | 8945 |
rs771048949 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101386867 | ATTTAAGATCATGAA[A/G]ATAGCCTCATATTTT | 8945 |
rs771050309 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546207 | GGAAATTACACCAAG[A/G]CAGACCACAGTCAGG | 8945 |
rs771070906 | snp | C/T | 3.32497e-05 | 0.00407722 | intron-variant | BTRC | GRCh38.p7 | 10:101550686 | CCTACCCTTTTTGTT[C/T]CTACTTCTTTAGGAG | 8945 |
rs771075313 | in-del | -/AAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101438423 | GAGCGAGACTGCCTC[-/AAAA]AAAAAAAAAAAAAAA | 8945 |
rs771076399 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101508116 | AACTATGTCAGAAAT[C/T]AGAAAATAATGAAAA | 8945 |
rs771086173 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101469880 | TGACATTCACTTTGC[A/C]TAATGTTTGTGAGAT | 8945 |
rs771087411 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530226 | GTGAAAGTCAGTTTC[A/T]TGCCTTAGACTTGAT | 8945 |
rs771087933 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493950 | CAGCATCAAATAGCT[C/T]TTCTGTCATGTTAAT | 8945 |
rs771135925 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101361434 | TATAGCACAGAAGTC[A/C]TTTCTAAATGTGTAT | 8945 |
rs771169420 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101409116 | CACATAATATAAAAT[C/T]AACCATTTTAAAGTG | 8945 |
rs771177027 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101390366 | TTCCGAGACGGAGTC[-/T]TCGCTTTGTTCCCCA | 8945 |
rs771199777 | snp | A/G | 5.25592e-05 | 0.00512609 | intron-variant | BTRC | GRCh38.p7 | 10:101532464 | TGTAGAAAGGTAGCA[A/G]AGGGAGCAAGAGTGA | 8945 |
rs771201056 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506624 | GATGCCAACTCTGCC[A/G]TAGTTAAATGTTAAA | 8945 |
rs771204419 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506407 | CAAAATTTAGCTCAT[-/G]TTTTTTTGTAATATT | 8945 |
rs771225694 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424641 | TTTGCCTGCAGGGCT[A/G]TCAGTGAAGAGGATC | 8945 |
rs771277322 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101462402 | AAAAAAACAGCAGCC[A/G]GGCAAGGTGGCTAAC | 8945 |
rs771282046 | snp | A/G | 4.06843e-05 | 0.00451004 | intron-variant | BTRC | GRCh38.p7 | 10:101521599 | TTTCCCTCATTTTCA[A/G]TACTAATCATTTTAT | 8945 |
rs771304026 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538337 | CTTTGGACCCCCGTG[C/T]TCCTGCAGGGACACT | 8945 |
rs771355300 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531393 | TATCAGCATTCTTCA[A/G]TCACAGTATGGTTAC | 8945 |
rs771370963 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101437597 | ATACTAGTAATTTCT[A/G]AATTTCACCTATATC | 8945 |
rs771375090 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355020 | TGTAATAAGGACAAG[A/G]TGATGAAAAGTAAGA | 8945 |
rs771407321 | snp | G/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534884 | GACAAGTACATTGTT[G/T]CTGCATCTGGGGATA | 8945 |
rs771431744 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434107 | CTTTAATGTCTGGAT[C/T]AAGAAAAGACAGCTG | 8945 |
rs771435906 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101501283 | TTTAAATTTATGTAC[G/T]CAATTTTATTTTAAC | 8945 |
rs771445032 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101464470 | ATTTAATGTTGTTTT[A/T]TTCATTGCCGTTTTA | 8945 |
rs771457900 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434886 | GTGATCTGCCCACCT[C/T]GGCCTCCTAAAGTCC | 8945 |
rs771488219 | snp | G/T | | | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354271 | GGTGGAGGCGCTGGC[G/T]TTGGCGGCGTCGCTG | 8945 |
rs771499076 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555466 | GTTGAGGATATTCTC[C/T]AAGTTGTCCTCTCTC | 8945 |
rs771527384 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101450492 | GTATCTCAGTGCTTA[A/G]TTGAGCTTGTTTATC | 8945 |
rs771532056 | snp | C/G | 1.66941e-05 | 0.00288908 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521677 | CAGTATGATTGTGCC[C/G]AAGCAACGGAAACTC | 8945 |
rs771540911 | snp | G/T | 1.67142e-05 | 0.00289081 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526022 | TGAAAGCTCGGGGAT[G/T]GGATCATATTGCTGA | 8945 |
rs771542912 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525900 | GACCACACTAGGGAC[A/G]ATGATGTGCCTTCAT | 8945 |
rs771570608 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453879 | AACATTTGAGGCTTT[G/T]TGGGAGATAGGATCT | 8945 |
rs771604511 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379279 | ACCTGACACATATGC[A/G]CCTCATCAATAAACT | 8945 |
rs771616848 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483479 | ATGCCTATAATCCCA[A/G]CTACTCAGGAGGCTG | 8945 |
rs771638508 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472179 | ATTCTAATTCAACCC[C/T]ACAGGGTTTGTTCTA | 8945 |
rs771667743 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101511349 | CTCAGCTCAGGTGTC[A/C]CTTCCTTTAGAGGCA | 8945 |
rs771689356 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535380 | AAGTACTTGTGAATT[C/T]GTAAGGACCTTAAAT | 8945 |
rs771690404 | in-del | -/TTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101396753 | AGGGTTTGTTGATGT[-/TTG]TTGTTTTTACATGAT | 8945 |
rs771697341 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420553 | GACATCCTCATCATT[C/T]TGCTCACTGCTGTTA | 8945 |
rs771703165 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497586 | TGGTGCGCACCTGTA[G/T]TCCCAGCTATTCAGG | 8945 |
rs771712602 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364061 | GCAGGGAGTAACTTG[C/G]ACAATACTATAGTGA | 8945 |
rs771763785 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380424 | GTCAAAAATGCAAAC[C/T]TGGGGAGGGCAGAAA | 8945 |
rs771765679 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363081 | GACTATAATTATTTA[A/G]CATGTACTATTTGCT | 8945 |
rs771789077 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | BTRC | GRCh38.p7 | 10:101534942 | CAGTAAGTTTCCAAC[C/T]TAGAATGGGGGAATT | 8945 |
rs771792005 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404436 | TTCCCCTTTTTAGTA[C/T]ACCAAGTAATTTTTG | 8945 |
rs771825772 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428321 | GAGTGCTTGGATTTC[A/T]TACAGTAGATATCTC | 8945 |
rs771849240 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530110 | ATACGAGTATTCCAG[A/G]GATGTGCTGTCATAA | 8945 |
rs771852072 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101519539 | TCTGTAACCCGTTGA[A/C]GCAAACTCTGTGCTT | 8945 |
rs771863146 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504222 | CAGACAATTAAACTT[C/T]ATTACTCCGCCTGAA | 8945 |
rs771869674 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473573 | TCTCCCGGGTTCAAG[C/T]GATTCTCCTCCCTCT | 8945 |
rs771891615 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443862 | ACTAGCCACAACTCC[A/G]ATTCGATTCACAGAG | 8945 |
rs771911675 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445325 | TACAGGTAAGAAGAT[C/T]AGAAAAAAAATTTTG | 8945 |
rs771938539 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458583 | ACTAAAAAGTTTCCA[A/G]TTGCCTCAACAGTGT | 8945 |
rs771945662 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101430169 | TTGGCCACTACTGCC[C/G]CTTTTGGGATTCTCT | 8945 |
rs771959408 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101534294 | AGCATCTTGGCCTAT[G/T]TCATTTCTGGCTCCT | 8945 |
rs771959765 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101552076 | ACTTTGCCATTTTTA[A/G]TATTCTTCCTGACTC | 8945 |
rs771965924 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101396862 | GGCTAGAGTGCAGTG[A/G]CATGATCTTGGCTCA | 8945 |
rs771970568 | snp | G/T | 1.65198e-05 | 0.00287395 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430372 | AGGTCTCTGTGGCTG[G/T]GCTGCTCCAGCCTGG | 8945 |
rs771973816 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361485 | GAAATAGAAAATATT[C/T]ACCAAAGTTTAACAA | 8945 |
rs771987926 | snp | A/G | 1.77517e-05 | 0.00297919 | intron-variant | BTRC | GRCh38.p7 | 10:101414669 | AGACCTTCCAGTGCC[A/G]TAAGCTATGAAGGTA | 8945 |
rs772000520 | in-del | -/AAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101467728 | GAGATGTTTATTAAT[-/AAAA]AAAATCACAATGCAT | 8945 |
rs772004975 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427878 | AAGTATTTATTGAAT[A/G]AATGATTAAAATATT | 8945 |
rs772010668 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556118 | CTATTGACAAGTAAT[-/A]AAAGTCTGGCCCTCA | 8945 |
rs772022762 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101405312 | ACAACTCCTCTGATC[A/G]GAGAGGAAGGTTTCC | 8945 |
rs772030602 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472139 | TTATATACTTTGAAA[C/T]CATTAGTTCACATTG | 8945 |
rs772040771 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101548021 | AACTTCATAAAGAAA[A/T]ATGCAAATTAAAATT | 8945 |
rs772050784 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101550928 | ATAACACTGTGGGTA[A/G]GAGACGGGATATTAG | 8945 |
rs772052784 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358437 | GGATAAATATATTCT[A/T]GTCCAGCCAATCCCA | 8945 |
rs772090723 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101414914 | AAAAGTTTTTAAAAA[-/C]TAAAAAAATTTATAA | 8945 |
rs772126299 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546118 | GCAGTACCATCAATC[A/G]AGTGGATATAATTGA | 8945 |
rs772137132 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504649 | CCTCTCCTTGCGTTC[C/T]TCCTTCTGCTTTCCC | 8945 |
rs772171108 | in-del | -/AACAGTGGA | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553962 | AAGTGACCCTGTGGC[-/AACAGTGGA]AACAGTGGATTCTCA | 8945 |
rs772171895 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363681 | CCACTGTGCCTGGCC[A/G]GGAAGTTCGTTTTAA | 8945 |
rs772176538 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443074 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTA | 8945 |
rs772178212 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101391896 | TGGTTAGTTCAATAT[C/T]ATTTTTACCTTGTAA | 8945 |
rs772184088 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468138 | CTTTGAGGAAGGAAG[A/G]CCGTATGGGGGGTTG | 8945 |
rs772185496 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381841 | TTTCTAAGAACAAGA[A/G]CATCCTTATTCCTAA | 8945 |
rs772226828 | snp | G/T | 5.20332e-05 | 0.00510038 | intron-variant | BTRC | GRCh38.p7 | 10:101532268 | GGTGTTTCCTAACAC[G/T]GCCTCTTTCCCATTC | 8945 |
rs772233689 | in-del | -/TC | | | intron-variant | BTRC | GRCh38.p7 | 10:101487087 | CTAAGTAATAAAATT[-/TC]TGTTTTGGAAAAAAT | 8945 |
rs772265470 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101520382 | TGTGCCTTTCACACT[A/G]AGAGTATATGTTAGT | 8945 |
rs772272252 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451729 | GCACCGTATGGCAGA[A/G]GGTCAGTAATCAGTG | 8945 |
rs772277127 | snp | A/C | 1.65285e-05 | 0.00287471 | intron-variant | BTRC | GRCh38.p7 | 10:101536677 | GCTAACAGAGTGTAA[A/C]AAAGAGAAAATCTAC | 8945 |
rs772279871 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101382339 | ATCCAATCATGTTAT[A/G]TATAATATCTCTTTA | 8945 |
rs772288731 | in-del | -/AAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101517446 | TAAAAGTAAATAAAT[-/AAAA]GAAAATAAGGCAAGC | 8945 |
rs772305924 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423938 | TTGCAGCTTTTAGAA[A/T]CCTTATTTTAGCCGG | 8945 |
rs772327269 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101466797 | TATAAAAGGAACTAC[A/G]TAAGTCTTTTAGAAG | 8945 |
rs772356382 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101477089 | TCAAGCGATTCTTCT[C/G]CCTCAGCCTCCCGAG | 8945 |
rs772379852 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352998 | GCTGGGATTACAAGC[A/G]TCAGTCACCGCGCCT | 8945 |
rs772394641 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101399539 | TCAGTACCTATATTC[C/T]GTGTGCCTAGCTGTT | 8945 |
rs772434552 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453265 | GATTTTTTCCTTCAG[A/G]TGGGTTGTCATTCTA | 8945 |
rs772457659 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530035 | GAATTAAATTTTTTA[C/T]CCAGCAGGAAGTGAT | 8945 |
rs772466975 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434232 | TGAAAGGGAAAGATA[-/T]TTTAATACCATTTTC | 8945 |
rs772522254 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460988 | GCTCACTGCAACCTC[A/G]GCCTCCTGGGTTCAG | 8945 |
rs772532571 | snp | A/G | 0.000165651 | 0.00909934 | intron-variant | BTRC | GRCh38.p7 | 10:101479478 | TAATATTGCTCATCA[A/G]TGTATATTACACCAC | 8945 |
rs772533654 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101540420 | CTTTGTCAAAAATGA[A/G]TTGACCATATATGTG | 8945 |
rs772540376 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514598 | GCTAGGATTATAGGC[A/G]TGTGCCATGATGTCC | 8945 |
rs772553406 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547164 | CAACAGGTTCATCAG[A/G]ATGTAACCCATTGTA | 8945 |
rs772574033 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408691 | TTTATGCCTTCTATT[A/G]GCTTACTAGGTACCT | 8945 |
rs772597929 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367347 | TGCTGGGATTACAGG[C/T]GTGAGCCACTCACTG | 8945 |
rs772601469 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453903 | AGGATCTTTCTTGTG[A/G]CCACTTACCTCTTCC | 8945 |
rs772642615 | snp | A/T | 1.65427e-05 | 0.00287595 | intron-variant | BTRC | GRCh38.p7 | 10:101534619 | AATATAGGTAACAGA[A/T]TGTAGCTTGAGTACC | 8945 |
rs772654417 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101418101 | GCTGGGCACAGTGGC[C/T]CACACCAGTAATCCC | 8945 |
rs772663113 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515416 | AATAGATCCAATTTC[C/T]GAATACAGTGTATCT | 8945 |
rs772683419 | in-del | -/GT | | | intron-variant | BTRC | GRCh38.p7 | 10:101527761 | CCTGTCTCTTTCTCT[-/GT]CTCTCTCTCTCTCTC | 8945 |
rs772704821 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424606 | TTCAGCTTTCGTATA[A/G]TAAATGCTGAGGCTA | 8945 |
rs772713712 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101458599 | TTGCCTCAACAGTGT[A/G]TGCTATACCTCTTTA | 8945 |
rs772755217 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101368394 | ATTATGAATTACCCA[A/C]CCTCAGGTATTCCAT | 8945 |
rs772761421 | snp | A/C | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534741 | ACTTGCGTTTCAATA[A/C]TGGCATGATGGTGAC | 8945 |
rs772765182 | snp | C/T | 3.31104e-05 | 0.00406867 | intron-variant | BTRC | GRCh38.p7 | 10:101479361 | TTCCAACAAATTCTC[C/T]TTACAGACATACAAC | 8945 |
rs772773723 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472316 | TCTCTTCTCTTCTCT[-/T]CTCTTCTCTCTCTTC | 8945 |
rs772778421 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423295 | CGCAATTCATTGCCA[A/T]ACAATGAATTGTTAG | 8945 |
rs772782701 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101496273 | GAATTGGAATTTCCA[A/G]ACTAGCACCAATTTT | 8945 |
rs772793762 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425731 | AGAAGGATTGCTTAA[C/G]TCCAGGAGGTCAAGG | 8945 |
rs772806067 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473606 | CTCCCAAGTAGCTGG[G/T]ATTACAGGCACTTGC | 8945 |
rs772829655 | snp | G/T | 1.75081e-05 | 0.00295867 | intron-variant | BTRC | GRCh38.p7 | 10:101521888 | ATGTCTACAAGTGTT[G/T]GTAAACCATTAATTT | 8945 |
rs772833143 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434920 | GATTACTGGCATGAG[C/G]CACTGCACCTGGCCT | 8945 |
rs772842671 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525553 | CTCTCCCCTAGTACA[-/T]TTAAAGGACATTTCT | 8945 |
rs772856203 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101549843 | ATCAGGGTGGTAACT[-/G]CCAGTGGTGTGCTAG | 8945 |
rs772857563 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472212 | TTTCTTTCTTTCCAT[A/G]TTTCATTTTTCTCCC | 8945 |
rs772857662 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101501622 | TGATACATAGAAAAA[A/T]TCCATGGGAAAGAGT | 8945 |
rs772868444 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511414 | CTTTACTTCTTTTCT[C/T]TTTCTTTTCTTTTTA | 8945 |
rs772879221 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101371352 | CCAGCTAATTTTTGT[A/C]TTTTTAGTAGAGACG | 8945 |
rs772880274 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101491060 | CAAGACTCTGTCTCA[-/AA]AAAAAAAAAAAACTC | 8945 |
rs772909161 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364197 | ACTCTCCTGATAGCA[C/G]TTTTTCATTTTGGTT | 8945 |
rs772948540 | snp | C/G | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535381 | AGTACTTGTGAATTT[C/G]TAAGGACCTTAAATG | 8945 |
rs772950534 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101444063 | TTTATTGAGCTAGAG[A/G]TCTGGCTTAGTAGCA | 8945 |
rs772983756 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101550365 | TCTCGGCTCACTGCA[A/G]CCTCCACCTCCCAGG | 8945 |
rs772987017 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101517459 | ATAAAAGAAAATAAG[C/G]CAAGCCTGAGCCTTG | 8945 |
rs773002126 | snp | G/T | 1.65004e-05 | 0.00287227 | intron-variant | BTRC | GRCh38.p7 | 10:101534945 | TAAGTTTCCAACTTA[G/T]AATGGGGGAATTCAT | 8945 |
rs773026787 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101546018 | ATAGATGCATCCACT[A/G]TTATAGTTGGAGACT | 8945 |
rs773059882 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521815 | TTACCAACATGGGCA[C/T]ATAAACTCGTATCTT | 8945 |
rs773060345 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101530647 | TATTCCATTTGTTTA[C/T]TGATATTATAATATT | 8945 |
rs773099123 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101534305 | CTATTTCATTTCTGG[C/T]TCCTGAGGGCTATCA | 8945 |
rs773116135 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101544938 | ACGTGCCCAGTGCAA[C/G]AACTTTTGGGTGGCT | 8945 |
rs773118049 | snp | C/G | 1.72276e-05 | 0.00293487 | intron-variant | BTRC | GRCh38.p7 | 10:101532278 | AACACTGCCTCTTTC[C/G]CATTCCTTCTTCTCA | 8945 |
rs773161509 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101358441 | AAATATATTCTTGTC[C/T]AGCCAATCCCAGAAT | 8945 |
rs773167186 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468345 | TCAAAGTCCATATGG[A/G]CCCAATTCATTTTGT | 8945 |
rs773170916 | snp | A/T | 1.77533e-05 | 0.00297932 | intron-variant | BTRC | GRCh38.p7 | 10:101414680 | TGCCATAAGCTATGA[A/T]GGTAGAAGACAGTGA | 8945 |
rs773180736 | snp | A/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405468 | TTACGATACTCCTTC[A/T]GCACTCCTTAAGCTA | 8945 |
rs773184051 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101467003 | GGAAAAAGCACATCA[C/T]TGACACAGAAAATGA | 8945 |
rs773186226 | snp | C/T | 1.65119e-05 | 0.00287327 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430379 | TGTGGCTGGGCTGCT[C/T]CAGCCTGGCGGACAG | 8945 |
rs773191257 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101389908 | GAGATTATAGGTATG[A/C]GCTAAATTTGCCAAA | 8945 |
rs773218641 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101372722 | ATACAAAAATTAGCC[A/G]GGCATGGTGGGGCAT | 8945 |
rs773241210 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483359 | CAGTACTTTGGGAGG[C/T]CGAGACGGGTGGATC | 8945 |
rs773273369 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520391 | CACACTAAGAGTATA[C/T]GTTAGTGATGTTAGA | 8945 |
rs773289839 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536014 | AAATTATTCCTAGAA[A/G]TCACTTGAATTGCTC | 8945 |
rs773291913 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101519540 | CTGTAACCCGTTGAA[A/G]CAAACTCTGTGCTTG | 8945 |
rs773298238 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101385549 | AAGAGTCTAGAAGGA[A/C]CATCTAATTCAAGGC | 8945 |
rs773306705 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527991 | TCCATCATTTTGCTA[A/G]GAGTGCTGGGACCAG | 8945 |
rs773321535 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101520340 | TTACAGGTATAAGCT[A/C]CTGCACCTGGCTGCT | 8945 |
rs773328045 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414267 | GATGGACTGTGTACA[C/T]GATGGTGGTCCCTTG | 8945 |
rs773353366 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490865 | GGAGTTCAAGGCCAG[C/T]CTGGCCAACAGGATG | 8945 |
rs773379261 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533985 | ATATTCTATAAAAGG[A/G]GGCTAAACTGGAAAA | 8945 |
rs773380085 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424612 | TTTCGTATAGTAAAT[A/G]CTGAGGCTAGCCCTT | 8945 |
rs773390872 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398457 | ACAGGTGCCCGACAC[G/T]GTGCCCAGATAATGT | 8945 |
rs773395268 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538332 | GGCTGCTTTGGACCC[C/T]CGTGCTCCTGCAGGG | 8945 |
rs773408160 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101487145 | AATCACCCTTATTAA[C/T]TGATTAGCATTTGTA | 8945 |
rs773412623 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530039 | TAAATTTTTTACCCA[A/G]CAGGAAGTGATTGCC | 8945 |
rs773426874 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101451745 | GGTCAGTAATCAGTG[C/T]CATCGTGCCTTTAAA | 8945 |
rs773432466 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101445786 | CCCAGAGGCCTTGGA[-/CT]CTCTTAATTTTGACA | 8945 |
rs773449774 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101432693 | AATTCACTGAAAACA[A/G/T]TTATACTCACAGTTT | 8945 |
rs773452364 | snp | C/T | 1.65828e-05 | 0.00287943 | missense, intron-variant | BTRC | GRCh38.p7 | 10:101531251 | GGGGACAGTATTTAT[C/T]CAAAAACAAACCTCC | 8945 |
rs773468427 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101529015 | GCTCAGTAATGGTAA[C/T]TCTTAAAAGTATAAT | 8945 |
rs773486824 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546155 | TAGAATGCTTCATCC[A/T]ACAGCAGCAGAATAC | 8945 |
rs773524221 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460976 | GGTGTGATCTCGGCT[C/T]ACTGCAACCTCGGCC | 8945 |
rs773570133 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534748 | TTTCAATAATGGCAT[C/G]ATGGTGACCTGCTCC | 8945 |
rs773579486 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459888 | ACTTTATAATTCAGT[A/T]TAGAGGAGTTTGCCA | 8945 |
rs773579568 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101477259 | TCCTGCCTTCGCCCC[A/C]CAAAGTGCTGGGATT | 8945 |
rs773604585 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101457766 | TTTTCCCCCTAAAAT[G/T]TATTTTTCACTTAAC | 8945 |
rs773626222 | snp | A/G | 1.65348e-05 | 0.00287526 | intron-variant | BTRC | GRCh38.p7 | 10:101536680 | AACAGAGTGTAAAAA[A/G]GAGAAAATCTACGTC | 8945 |
rs773636091 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383393 | TCTATAAGTCTTCCT[-/T]TTTTAAAAAAAAAAA | 8945 |
rs773646749 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101510430 | CAGGAGAATGGCGTG[A/C]ACCCAGGAGTTGGAG | 8945 |
rs773656050 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554357 | TGCCTGTATCTTTGC[C/G]AAGACCGTGATCAAG | 8945 |
rs773677334 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101368015 | CTTTATGCTATGGTT[G/T]GAATATAGCTTGTTT | 8945 |
rs773685974 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101537481 | TGCAGTGAGCCAAGA[C/T]TGCGCCACCACACTC | 8945 |
rs773687234 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423951 | AATCCTTATTTTAGC[C/T]GGGTGAGGTGGCTCG | 8945 |
rs773730872 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101393550 | ACATAATTCATCAGT[C/T]CTGTCAAAGTACATC | 8945 |
rs773746530 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555350 | GCTCTCCAATCTAGG[C/T]TCAGTTGAAGGAATA | 8945 |
rs773749384 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514649 | GTAGAGATGGGGTTT[C/T]ACCATGTTGGCCAGG | 8945 |
rs773784415 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499942 | CTGAAAGAAAAAGCT[C/G]TCTGCAATACAGCAG | 8945 |
rs773806205 | snp | A/G | 3.29663e-05 | 0.00405981 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521726 | GAAAAGGAACTGTGT[A/G]TCAAATACTTTGAGC | 8945 |
rs773806546 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101539119 | TTAGTTCTGCAGCCT[A/G]TTCATGAGGTAGTGC | 8945 |
rs773836101 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101362973 | TGTAGGTTATGTGCC[A/G]TTTAAGGCACTATAA | 8945 |
rs773847300 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377416 | TACCCATGAGGGAGA[A/G]TTGCGTGATAAATGT | 8945 |
rs773848311 | snp | A/C/T | 7.54895e-05 | 0.0061433 | intron-variant | BTRC | GRCh38.p7 | 10:101521609 | TTTCAATACTAATCA[A/C/T]TTTATGTTTCTTTTA | 8945 |
rs773857124 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433802 | TTACTCTGGCTATAA[A/T]AAGGATAATTTCAGT | 8945 |
rs773860740 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101472006 | AGTATTTCCATCTTA[C/T]AGTTTCCCTGGTCAG | 8945 |
rs773900128 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375541 | GCAGGAGAATAATGG[C/T]AGGGAGTCTGGGGCA | 8945 |
rs773900474 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101405759 | CTTACATGGAACTAG[-/AA]AACCCCTTCTAGTTA | 8945 |
rs773917419 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | BTRC | GRCh38.p7 | 10:101353821 | CCCCTCCCGTTTCTC[A/G]TCCTTAGAGGCTGTA | 8945 |
rs773940070 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101450107 | AAGTTTAAATGGACT[A/G]TTACTTCTGATGTGG | 8945 |
rs773941637 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416757 | AATATCAGGTTAACC[A/G]TAATGCATTTCCCTT | 8945 |
rs773963944 | snp | G/T | 1.64784e-05 | 0.00287035 | intron-variant | BTRC | GRCh38.p7 | 10:101534918 | CTATAAAGGTAATAA[G/T]GCATTTTTCAGTAAG | 8945 |
rs773968074 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554073 | AGGCAGAGGGGGTGG[A/G]GAGAAGTTTCCTGGG | 8945 |
rs773981501 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101448079 | TAATCAAATTAATTG[C/T]AGGATTTGTCAGAAA | 8945 |
rs773983864 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527548 | GTTTGAGCCCAGGAG[G/T]TTGATACCAGGCTGG | 8945 |
rs773999513 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101469377 | GAATGTCTAGAAAAT[-/A]AAGTCCTATATATAG | 8945 |
rs774019927 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101457243 | GAGATGAAGTGAGGT[A/G]AATGACCTAGGCATT | 8945 |
rs774068459 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361672 | AGAATTTCTGGATAA[C/T]TAGAATAGTCTGAGG | 8945 |
rs774123183 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101422803 | TTATTATTTCTGAGG[G/T]CTCTGTTCTGTTCCA | 8945 |
rs774139790 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359268 | TTGATTACCAGGTAG[G/T]GGGATGAACATCTGA | 8945 |
rs774158818 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369489 | ATTGAGCATTTTCTT[C/G]TTTACTGAAAGATAC | 8945 |
rs774182656 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101487583 | GAGAGCAAATTAGAA[A/C]AATCAGTTTACACAG | 8945 |
rs774192286 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534789 | CCATTGCTGTATGGG[A/T]TATGGCCTCCCCAAC | 8945 |
rs774234270 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101550234 | GTATTTGACTTTTCC[A/T]TGCTGCCTTTAGCCA | 8945 |
rs774234466 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557093 | TGATGGGACAGGCCT[A/G]ACAACACATGTAAGC | 8945 |
rs774240875 | snp | C/T | 3.30349e-05 | 0.00406403 | intron-variant | BTRC | GRCh38.p7 | 10:101536672 | AGTGTGCTAACAGAG[C/T]GTAAAAAAGAGAAAA | 8945 |
rs774243430 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443671 | GCCATTATTTTGTAG[A/G]CTAATTTGTTCTTCA | 8945 |
rs774247651 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511306 | GATCTTCCCCAAGAT[C/T]TTCACAAGACTGACA | 8945 |
rs774255134 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450592 | TTGACTTGAAAAACA[C/T]TTGATCTCTTACATT | 8945 |
rs774294815 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370974 | ATTTAAACATTTTTT[A/G]TTGTGGTAAAATACA | 8945 |
rs774323634 | snp | C/G | 1.74324e-05 | 0.00295227 | intron-variant | BTRC | GRCh38.p7 | 10:101532260 | TGATTCTAGGTGTTT[C/G]CTAACACTGCCTCTT | 8945 |
rs774328368 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101408069 | ATTATGAATTAGATA[C/T]TTCACTTTTTTGTAT | 8945 |
rs774330830 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519311 | TGTCAAACTCCTGAC[C/T]TTAGGTGATCCACCC | 8945 |
rs774349776 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531667 | CACATGTTGCAGTGA[A/G]CCAAGATCGCACCAC | 8945 |
rs774349991 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389807 | TTTTTAAATTTTTTG[C/T]ACAGACAGGGTCTCA | 8945 |
rs774378653 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101354785 | TAGAATGAGGAGGGA[-/G]GATAGCCTTTGCCTT | 8945 |
rs774379184 | snp | C/T | 0.000421807 | 0.0145164 | synonymous-codon, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354192 | GATTATGGACCCGGC[C/T]GAGGCGGTGCTGCAA | 8945 |
rs774380346 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101356839 | AGAGTCAGTTTTAAG[A/G]AAGGAAGATAGGCCG | 8945 |
rs774416229 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435253 | ACATGGATCATAAGT[A/G]TACTCTTAGGTGAGT | 8945 |
rs774419860 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101481945 | GTCAATGTCAAATAA[A/G]AACACATAGCTGAAA | 8945 |
rs774434326 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101551377 | TAAAAGGAATATAAA[A/C]AGTAGCTTTTATATC | 8945 |
rs774436140 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101526662 | GCGTGCACCTGTAAT[-/C]CCAGCTACTGTAGAG | 8945 |
rs774471229 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101480080 | AATTACTGAGGAATT[C/T]TGACTAAAATTCAAG | 8945 |
rs774475844 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427780 | GGATCCACCTGCCTC[A/G]CCCTCCCAAAGTGCT | 8945 |
rs774530525 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101466175 | TGAGTAAATTGTGAC[C/T]GTTGTCTAATCCCTC | 8945 |
rs774532059 | snp | A/G | 1.65045e-05 | 0.00287263 | intron-variant, missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101461993 | CAGAATTCCTCAGAG[A/G]GAGAAGACTGTAATA | 8945 |
rs774540273 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101475212 | AATTATAAGAATAAA[A/G]CAAGTTGGTAAATTT | 8945 |
rs774548901 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514773 | ATTGAATTATCTTGG[C/T]ATCTTTCTTGAAAGT | 8945 |
rs774550640 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547425 | GGCTCACTGCAACCT[C/G]CACCTCCTGGGTGCA | 8945 |
rs774551818 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101411221 | CTGGTCTCGAACTCC[G/T]GACCTCAAGAAATCT | 8945 |
rs774555528 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101504610 | CCTCTTCCTCTTCTA[C/T]CCTCTTCTCTAGCCC | 8945 |
rs774566312 | in-del | -/AC | | | intron-variant | BTRC | GRCh38.p7 | 10:101380964 | CTGTAAGCCATTGTA[-/AC]ACAATGGTATTTGTA | 8945 |
rs774577646 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101465020 | TTTTTTTAAGGTAGG[A/C]CATAGTATATAAGCT | 8945 |
rs774599424 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381269 | CTGATTTACAAATGT[C/G]GAAACTGAGGCACAG | 8945 |
rs774606784 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503044 | CTAAGTATTGTAACT[A/G]TCACCATTTTATAGA | 8945 |
rs774656586 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497943 | GAGAATTGCTTGAAC[C/T]TGGGAGGCAGAGCCT | 8945 |
rs774690874 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101412162 | TTCACTGTATGTATA[C/T]AGGACTTAGTATTCA | 8945 |
rs774713093 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490607 | TACCAGGATACTTCC[C/G]CCATCGCATTGTGTA | 8945 |
rs774772585 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101364559 | ATCAGGTGCTGATAT[A/G]TTTAGATGTCTGGAA | 8945 |
rs774784817 | snp | A/G | 4.99313e-05 | 0.00499632 | intron-variant | BTRC | GRCh38.p7 | 10:101479351 | AAAAACCTGTTTCCA[A/G]CAAATTCTCTTTACA | 8945 |
rs774795799 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101367639 | GAAACCACTCTCTTA[C/T]AATATCTGTAGATTA | 8945 |
rs774808922 | in-del | -/GAAAAC | | | intron-variant | BTRC | GRCh38.p7 | 10:101397287 | TCAAATGGGGAAAAT[-/GAAAAC]AGCCCAGATAAGCTG | 8945 |
rs774811168 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101552855 | CCCTGCCCTGCCATT[C/G]TACAGGGCAAGTGAA | 8945 |
rs774814497 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101527789 | TCTCTCTCTCTCTCT[C/T]TCACATACACACACA | 8945 |
rs774824429 | in-del | -/ATCAGTAGCA | | | intron-variant | BTRC | GRCh38.p7 | 10:101531941 | CCTCCTTAGAAGTTC[-/ATCAGTAGCA]ATCAGTAGCAATGGC | 8945 |
rs774846146 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101436571 | AGTGAGCCATGATTG[C/T]GACACTGCATTCTAG | 8945 |
rs774851389 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101382252 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 8945 |
rs774869773 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101467210 | TAAAAAAAAAAAAAA[-/C]ACAGAATTTGCTTCC | 8945 |
rs774899846 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392177 | TAGCGACTGGGTTTC[A/T]CCATGTTGGTCAGGG | 8945 |
rs774900731 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428830 | TGCAGCCCATTATCT[A/T]TCTATCTTTATTTAG | 8945 |
rs774921343 | in-del | -/C | 1.64766e-05 | 0.0028702 | frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550815 | GCTGCCCAAGCTGAA[-/C]CCCCCCCGTTCCCCT | 8945 |
rs774961881 | in-del | -/TTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101399323 | TAACTAGAATCACCT[-/TTTT]TTTTTTTTTTTTTTT | 8945 |
rs774971820 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533047 | GAGAGTGATCATAAC[A/G]GGATCATCGGATTCC | 8945 |
rs774979296 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101533167 | ATCGGCACAGTTCTG[A/C]AACTAAAGAAGAATA | 8945 |
rs774985059 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101459265 | TAACTGTGTTGCTGA[A/G]CTTTCCTGGGTGATG | 8945 |
rs774991791 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101521941 | ATCTCCAGCTATATA[G/T]CTCTCTTTAAAAGTC | 8945 |
rs774996680 | in-del | -/ATAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101420060 | TGGGTATATGTGTAC[-/ATAT]ATATATATATATCAT | 8945 |
rs775005115 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400607 | TGTCAAAGGATTTTA[C/G]TCTGGCTTATTTGGC | 8945 |
rs775010815 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101528971 | AACTCTGTAGTTTTC[C/T]CTCTTGAATAATACT | 8945 |
rs775011803 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534779 | AAAGATCGTTCCATT[A/G]CTGTATGGGATATGG | 8945 |
rs775069170 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101460687 | TTTATCTCTCAGTAT[C/T]TTTCAAAATGTAATA | 8945 |
rs775085669 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401269 | AGTTTTACTCTTATC[A/G]CGTGAATGAGCATTC | 8945 |
rs775111439 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101469033 | GTAGTTTTCAGCAAG[A/G]CATCTTACTAGTTTA | 8945 |
rs775117789 | in-del | -/CTTAATCTCTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101356436 | TAACATTCTCAGCTA[-/CTTAATCTCTG]CTTTGTACCAGTGAG | 8945 |
rs775155707 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474483 | TGCACAGGCCTTTCA[A/G]CCCTCCAGCTGTTGC | 8945 |
rs775187144 | in-del | -/AGAC | 1.65201e-05 | 0.00287398 | intron-variant, frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101462053 | GAGAAGAATTCACTT[-/AGAC]AGGTATGAAATTCAG | 8945 |
rs775206964 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445698 | GGAGTTGTGTATAAT[C/T]GCTTTGGTTTAATCA | 8945 |
rs775208631 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416608 | TGTCCTATATGCACC[C/G]TATACTCCAGTCTTT | 8945 |
rs775210690 | snp | C/T | 0.000234859 | 0.0108339 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354173 | CGGACCCAGTGGCCT[C/T]GGCGATTATGGACCC | 8945 |
rs775211946 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101375444 | GTGAGCCAATGAAAC[C/T]TCTTTTCTTATAAAT | 8945 |
rs775240433 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524637 | GTGAAATGATCAGGA[A/G]CAATTTGATGGCACC | 8945 |
rs775253913 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101432026 | TAAGGGCATGCAGTG[A/G]TGGTAGCTGCTTTTA | 8945 |
rs775269208 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101470010 | GCCATTTCCATCATT[A/G]TAAGTGAAGTTACTA | 8945 |
rs775346915 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101498451 | TGAGCCACCACACCC[A/G]GCCTCCGAAGCTGCT | 8945 |
rs775350356 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444998 | GATATTACACAATGA[A/T]TGGGGCAGGAGGGTA | 8945 |
rs775352494 | snp | A/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101477229 | TGGTCTCAAACTTCT[A/G/T]ATCTCAAGTGATCCT | 8945 |
rs775364174 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101426390 | TGTCTTGTAATAATC[A/G]GGAATGCATCCTCTG | 8945 |
rs775381362 | snp | A/G | 1.70203e-05 | 0.00291716 | intron-variant | BTRC | GRCh38.p7 | 10:101531196 | TGTATTTAAATATAT[A/G]ATGTCATGATTTTCA | 8945 |
rs775394803 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101531516 | GCTGAGGTCAGGAGT[C/T]TGAGACCAGCCTGGC | 8945 |
rs775395165 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463334 | CAGGCATGAGCCACT[A/G]TTCCCGACCTAATTT | 8945 |
rs775474790 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101511400 | AAGTAGGCTGCACTC[-/TT]TACTTCTTTTCTTTT | 8945 |
rs775475473 | in-del | -/TG | | | intron-variant | BTRC | GRCh38.p7 | 10:101382680 | AGCAAACTTGGAGAC[-/TG]TGTAAATATCTTATT | 8945 |
rs775489273 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441615 | CCGGGCGTGGTGGCT[C/T]ATGCCTATAATCCCA | 8945 |
rs775507506 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514641 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 8945 |
rs775550354 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101448935 | GAGAGGAATGGTATT[G/T]GTAATTTTAAAGACC | 8945 |
rs775565035 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101494160 | CTGCTCTTAGAATGA[A/G]TGTGGCCAGGTTAAT | 8945 |
rs775567120 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101468710 | ATCTTGTTATGCTAT[-/A]AGGGCTGCTGAACAG | 8945 |
rs775568005 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547634 | GTGAGCCACTGCACC[C/T]GGCCATGTATGGTCT | 8945 |
rs775589029 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101355491 | TGTATTTCCTAGGTG[G/T]AAAACCAGACTTTGT | 8945 |
rs775592424 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101387651 | CCTGCCTCACCTTCC[C/T]GAGTTGTTGGGATTA | 8945 |
rs775620131 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492757 | TTTTCTTACGAAAGA[A/T]GGAGTATAGATACCA | 8945 |
rs775623130 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501535 | AAAACTTTTTGATGA[A/G]TGGTTTGTTTCCAGA | 8945 |
rs775649037 | snp | A/G | 3.3123e-05 | 0.00406945 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101535436 | TGCAGTACAGGGACA[A/G]GCTGGTAGTGAGTGG | 8945 |
rs775681800 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101541451 | TTTTTTAGTAGAGAC[A/G]GGGTTTCATCATGTT | 8945 |
rs775702547 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101370730 | TGTACCACCAAACAT[C/T]GGCTAATTTTTTTGC | 8945 |
rs775717834 | in-del | -/AG | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557391 | AGACTGAGGGAGTGC[-/AG]AGATAGAATACCTTT | 8945 |
rs775732081 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483937 | ATTGGCTTTATTAAA[C/T]TATTACTGCAAATTT | 8945 |
rs775737750 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101356641 | TGCCTGCTGTTTTGG[C/T]TGCCATTTGAGAAAA | 8945 |
rs775774044 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435077 | AATAGGCAGAAACTG[A/G]ATTTGAATCTAGTAT | 8945 |
rs775833317 | snp | C/T | 1.64953e-05 | 0.00287182 | stop-gained, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430408 | AGCATGCCTTCGCTG[C/T]GATGCCTGTATAACC | 8945 |
rs775848897 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101511576 | TTTTGTTTTGTTTTG[C/T]GACAGAGTCTCACTC | 8945 |
rs775861217 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380661 | TTGAAATGACACTTA[C/T]TTTTCCATTTCCTTG | 8945 |
rs775875776 | in-del | -/TTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101387529 | ATACCTTCATGGGAC[-/TTT]TTTTTTTTTTTTTTT | 8945 |
rs775888373 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410873 | TGTGTTATTATTGTC[A/G]TACGTTTTGTTTTCA | 8945 |
rs775903833 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488935 | ACTAATGTAGATTAT[A/G]TGTATCATAATAGGT | 8945 |
rs775907313 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379503 | AGAATTCATACTAAA[A/G]GATCAACTGAGACTT | 8945 |
rs775912852 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555640 | CACTTACCATCTCTG[C/T]ATGATTTCAGTGGGA | 8945 |
rs775941333 | snp | A/C/T | 4.94314e-05 | 0.00497128 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550820 | CCCAAGCTGAACCCC[A/C/T]CCGTTCCCCTTCTCG | 8945 |
rs775948193 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488007 | TATAGACTGTAATTC[C/T]ATCAGGAGTCATTTG | 8945 |
rs775983898 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101532492 | TGACCACATTCATAG[C/T]GCAGTCTAAAGCATA | 8945 |
rs775987518 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101450367 | ACATTAAAATGTTGT[A/G]TTGTGATATTTTCGG | 8945 |
rs775993278 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533032 | TCTCCAGTATGATGA[A/G]AGAGTGATCATAACA | 8945 |
rs776006902 | in-del | -/CT | | | intron-variant | BTRC | GRCh38.p7 | 10:101368303 | GGAAGCCGCTTGAGA[-/CT]CTTACCAGGAGCAGA | 8945 |
rs776026125 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101530765 | CCCAGAAGGTTACTC[-/TT]TGACATGGGACTCCT | 8945 |
rs776051272 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404563 | CTTCAGTCTACAAGT[C/T]GAGATTTCTGTAGGA | 8945 |
rs776054492 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101527623 | GCTGGGCCTGGTGGC[A/G]CATGCCTGTAATCCC | 8945 |
rs776067009 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101363500 | GTCTTACTCTGTCAC[C/G]CAGGCTGGAGTGCAG | 8945 |
rs776126545 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536279 | ATTGAATTCGTTTTT[A/G]TGCCTGGAAGAACCT | 8945 |
rs776137879 | in-del | -/CGC/CGCTGTTTTACAGT | 3.56403e-05 | 0.00422127 | intron-variant | BTRC | GRCh38.p7 | 10:101414731 | GTGGGCCTAGGCTAA[-/CGC/CGCTGTTTTACAGT]TGTAATGTGTGTGTT | 8945 |
rs776147879 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101544654 | CACATAATCCTCTTG[A/C]CTCACAACCTCCTGA | 8945 |
rs776150394 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101428509 | GCTGTTTTGCTTGGT[A/G]TGTTATCTGGTGATG | 8945 |
rs776163285 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101547664 | TATTATTGCCCTTAT[-/A]GTTTAGCAATTTCAT | 8945 |
rs776164610 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421126 | TTCTAGTCATTCAAG[C/T]TTGAAATGTTGAAGT | 8945 |
rs776181591 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550826 | CTGAACCCCCCCGTT[C/T]CCCTTCTCGAACATA | 8945 |
rs776214939 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101552575 | GATCTCATCTCATTG[C/T]AGAAGACTCAAATTT | 8945 |
rs776219067 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101414421 | GCTAGTCATAAAAAA[A/G]TGTAGTACATACTAT | 8945 |
rs776224074 | snp | A/C | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533061 | CAGGATCATCGGATT[A/C]CACGGTCAGGTAGAA | 8945 |
rs776229910 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101444392 | AAAGAGTCTATTGCA[C/T]ACAAGGTATAAAGTG | 8945 |
rs776287210 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101420062 | GGTATATGTGTACAT[-/AT]ATATATATATATCAT | 8945 |
rs776287470 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101458736 | TGATGTTTTCTTATA[A/C]GTAGATTTAAGTTTT | 8945 |
rs776292989 | snp | A/G | 1.65138e-05 | 0.00287343 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526057 | ATTCTGTCATACCTG[A/G]ATGCCAAATCACTAT | 8945 |
rs776300907 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101467246 | TAGCTCTGTAATGTT[A/C]ATATATGATGGCATT | 8945 |
rs776312355 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101428399 | TATTTTTCTATTTAG[C/T]TGCTGTTTATAAAAT | 8945 |
rs776314656 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101497836 | AACATCTTGGCCAAC[A/C]TGGTGAAACCCCATC | 8945 |
rs776354693 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101392070 | CTGCAACTTCTGCCT[C/G]CCGGGTTCAAGTGTT | 8945 |
rs776376391 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373475 | GAAAAAGAGTAAAAT[A/G]TAGCTGGCATCAGTC | 8945 |
rs776382905 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551660 | TGTGCCTCAGTTCTC[A/G]TGGCGGAAGTACATG | 8945 |
rs776426151 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101484424 | GAAGAATTATTGCCA[A/G]CCATGAACAGTGCAA | 8945 |
rs776450026 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101468608 | ACCATATTCTTGTGT[A/G]GGACATGATTTGATG | 8945 |
rs776491052 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520599 | TTATGTCCAAAAAGG[C/T]ACCACAGAGTCTCAG | 8945 |
rs776492963 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445967 | GAGAATACTGAATAG[A/G]AATGATAATGTGGCA | 8945 |
rs776517432 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant | BTRC | GRCh38.p7 | 10:101536507 | GGCTTAGAAAAGAAT[A/G]CGTGAAAATTCACCT | 8945 |
rs776519820 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101546254 | TAAAAAATTTACAAG[A/C]GTAGAAATCATACAG | 8945 |
rs776529269 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520527 | ACTTCATGGGAAATA[C/T]GGAATATTTTATGTT | 8945 |
rs776563405 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101467330 | ATCAGGCAGGCAGGG[-/T]TTTTTTTTTTTTTTT | 8945 |
rs776563787 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101491139 | ACCTGCCTTATTAAC[A/G]TAGTATACAGATCTT | 8945 |
rs776593953 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492698 | GGAGACAAGGTAGTT[C/T]CTGAAATGTATTGAA | 8945 |
rs776612759 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101453447 | TGGTGTGAAATGTTC[A/G]CTTGTAGCTTTGGAG | 8945 |
rs776642112 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506700 | AGACTATTTCAATCT[C/G]AGTTGACTAACCCTA | 8945 |
rs776643514 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101478481 | TTTAAAATTTTTTCA[-/T]TTTATTGTTCTGAAT | 8945 |
rs776644344 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101547514 | CTCAGCTGATCTTTG[C/T]ATTTTTAGTAGAGAC | 8945 |
rs776644962 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101454941 | TGAAAACCAGGCCTA[C/G]AACTTCATATTTGAT | 8945 |
rs776648761 | snp | C/T | 8.25294e-05 | 0.00642323 | missense, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101430388 | GCTGCTCCAGCCTGG[C/T]GGACAGCATGCCTTC | 8945 |
rs776649452 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101416426 | GAAATCATTCTTCAC[A/G]GGGTGTTGAATATTC | 8945 |
rs776652297 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101359792 | TTTGGTAGAGACAGG[G/T]CTTTTCCATGTTGGT | 8945 |
rs776681750 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101540846 | GTTTGGAGAATATTG[A/G]CTTCTGAACAATATT | 8945 |
rs776702450 | in-del | -/TCTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101388386 | TTTGTAGAGACAGGG[-/TCTC]TCTCTGTTGCCCAGC | 8945 |
rs776728150 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101401078 | AATACAATAAATTCT[A/G]TGGCAATAAAAGAAT | 8945 |
rs776732107 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101444131 | ATATCTCATCTCAGC[-/A]AAAAAGTGATAATGT | 8945 |
rs776742730 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383152 | CATTGCAGCCTTGAC[C/T]TCCCAGGCTCAAGTG | 8945 |
rs776755244 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101477451 | ATAAGTTTGCTTTTC[A/T]TAAAGTATAACTATA | 8945 |
rs776795880 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101506696 | CAGCAGACTATTTCA[A/T]TCTCAGTTGACTAAC | 8945 |
rs776797530 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101434025 | GCATATAATGCAAAT[-/A]ACATTTTTATGAAAA | 8945 |
rs776810048 | snp | C/T | 1.77552e-05 | 0.00297948 | intron-variant | BTRC | GRCh38.p7 | 10:101414690 | TATGAAGGTAGAAGA[C/T]AGTGATATTGATGAT | 8945 |
rs776813453 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101505639 | AATAAAAAAAAAAAA[-/AT]ATAATAATAAAAAAA | 8945 |
rs776816147 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101461028 | CTGCCTCAGACTCTC[A/G]AGTAGCTGGGATTAC | 8945 |
rs776816261 | in-del | -/TTG | | | intron-variant | BTRC | GRCh38.p7 | 10:101523302 | GATATCTCATAAGCC[-/TTG]TTGTGGTGTTAAATA | 8945 |
rs776829334 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101381963 | TATCCTAAGAATGTC[-/TTTTTTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTGAGAT | 8945 |
rs776847117 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101530358 | TTCAAAGCATAGTTG[C/G]ACTGATTAGCAGCAG | 8945 |
rs776875488 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369282 | TCGAGTACACTGGTG[C/T]GATCATAGCTCACTG | 8945 |
rs776888544 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101404521 | TTGAAAATGTTGATA[-/T]TTTTGTCAGGCATTC | 8945 |
rs776896072 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101479624 | GCAAGTTAGATTCTC[C/T]ACCTCTTAATTGCAA | 8945 |
rs776902865 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516892 | CAGTAGCACCCAACT[C/T]ATGTCCATTTCCACC | 8945 |
rs776927122 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101448535 | ATAGAAGACTTCTCA[C/T]TCAAATTTTAAATCC | 8945 |
rs776928629 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101538584 | TATGGAGAGAAATGT[-/G]GCAGCTGTTTAACAG | 8945 |
rs776970286 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101434123 | AAGAAAAGACAGCTG[C/G]ATTCTCATGTCTGCT | 8945 |
rs776984934 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101524580 | GGGTTTGTTTGGAGT[A/G]TTAGGTGAAATTACT | 8945 |
rs776986651 | snp | C/T | 1.6609e-05 | 0.0028817 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101521684 | ATTGTGCCCAAGCAA[C/T]GGAAACTCTCAGCAA | 8945 |
rs777015185 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101395206 | CAAACTCTAAGGAAA[A/G]AAGAAGGTAGGGTTG | 8945 |
rs777020158 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101424656 | ATCAGTGAAGAGGAT[A/C]TGTGACATTACTCCA | 8945 |
rs777020701 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101355336 | TGAAGCACAGTGTGA[A/G]CAAAGATTGGATTTT | 8945 |
rs777047410 | snp | A/T | 1.67668e-05 | 0.00289537 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532307 | CAGACAATAGAATCT[A/T]ATTGGAGATGTGGAA | 8945 |
rs777059061 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101432761 | GAAGAGACACATAGG[A/G]CAGAATCTCGGAAGG | 8945 |
rs777072254 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483669 | TTTGGAGGCATTGAG[A/G]TACCTTTTTGTTTTT | 8945 |
rs777074566 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101539819 | AGAGTTCCAGTTACT[C/T]CACATTCTTGCCAGT | 8945 |
rs777105523 | snp | A/C | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536588 | ACGAGTGTTAGAAGG[A/C]CATGAGGAATTGGTG | 8945 |
rs777120612 | snp | A/G | 1.66015e-05 | 0.00288105 | intron-variant | BTRC | GRCh38.p7 | 10:101550689 | ACCCTTTTTGTTTCT[A/G]CTTCTTTAGGAGCAT | 8945 |
rs777125606 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101442636 | TTCCTTTAACTGGTG[-/A]AAAAAAATCGAGTTG | 8945 |
rs777128181 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410546 | TTGAATCTGGGAGTC[A/G]GAGATTGCAGTGAGC | 8945 |
rs777138158 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398938 | CCTTTCATGTAGGTA[C/T]AGAGAAGAAACCTTT | 8945 |
rs777147023 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451500 | CATGCGCTTTGACAT[A/G]ACATATCTGTAATCT | 8945 |
rs777174022 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101541898 | ATTGGTTTGTTGCTT[C/T]ATTTTCTGTGTCTCT | 8945 |
rs777199100 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101452209 | AGTGCACTATGACAA[C/T]TAATCAGTTTCTGCA | 8945 |
rs777201178 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377645 | CTCGATTCTTGATGC[G/T]TTTATTGATGGAGGA | 8945 |
rs777223538 | snp | A/G | 4.97006e-05 | 0.00498476 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526038 | GGATCATATTGCTGA[A/G]AACATTCTGTCATAC | 8945 |
rs777273244 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487821 | GCACCACAGCTGCAC[A/G]ATGCCAGGCTCAGTT | 8945 |
rs777296923 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485939 | CCCGCACAGAGAGAT[C/G]ACATGGCTTCTCCAA | 8945 |
rs777310716 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101380507 | CAGAGGTACTCCTCA[A/C]TTCCCAGACGGTGGG | 8945 |
rs777322637 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101486184 | CTAATCTTACCGGTG[G/T]GAGCAAGCGGCTGTT | 8945 |
rs777374508 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101458529 | AAACAATCAGGAAAT[G/T]AATATTGATACAGTG | 8945 |
rs777380076 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101490233 | TCACTCCCTCCTTCC[C/G]TCCCTCACTCCCTGC | 8945 |
rs777401476 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512657 | TATTTTTCCCTCCTG[A/G]CCCAGGCTGCAGCTT | 8945 |
rs777424111 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101437682 | TATCTCATAGATAGC[A/T]GCTCACATGTTTTTG | 8945 |
rs777433377 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101488884 | TTAGGTATGAGGTGA[A/T]CTTTTCTCATAGGAC | 8945 |
rs777459910 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101456402 | TAGATATGTTCAAAG[-/A]AAAAAAAAGGAATGA | 8945 |
rs777461229 | snp | A/G | 1.82623e-05 | 0.00302173 | intron-variant | BTRC | GRCh38.p7 | 10:101535524 | ATTATGCTCCCATTC[A/G]TTATTAATGCACAGA | 8945 |
rs777464455 | in-del | -/AA | 1.64749e-05 | 0.00287005 | frameshift-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536625 | ATTCGATTTGATAAC[-/AA]GAGGATAGTCAGTGG | 8945 |
rs777493638 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352752 | GACAGAGTCTCGTTC[C/T]GTTGCCCAGCCTGGA | 8945 |
rs777495078 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101354866 | GAAGAGGCCTCACTA[A/G]AGAAGATAAGGACTG | 8945 |
rs777498005 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101545768 | TACTTTGTTATGGCA[C/T]CCCTAGCCCTGATGG | 8945 |
rs777521126 | snp | A/G | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352296 | TATTATGTATTAAGT[A/G]TCATGCTGAGTTTTG | 8945 |
rs777534121 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101375021 | GAGTTGGGGAAAAGA[A/G]ATTGACTAGGTGTCT | 8945 |
rs777547520 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474721 | TTCAGATTGAATTCT[A/G]GTCACCCTGCACCAA | 8945 |
rs777556782 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101484102 | GTTTGGGAAATAAAC[A/C]CCTTCAGTAGCCCTT | 8945 |
rs777569313 | in-del | -/GGT | 0.00010141 | 0.00712001 | intron-variant, cds-indel, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354239 | TTATGGTGAGGAGAC[-/GGT]GGAGGCCGGGGAACG | 8945 |
rs777573068 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408132 | TTGTAACATATTTCA[A/G]TTTGGACTAGCCACC | 8945 |
rs777594979 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101513832 | GTAAGTATATGTTTA[A/G]CTTTACAAAAAACTG | 8945 |
rs777600441 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441226 | ATATGCTTTATGGAG[-/T]TTTCTAAATCTGGTA | 8945 |
rs777636294 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101472357 | GTTTTTGGTAGAGAT[A/G]GGGTCTCTCCCTATG | 8945 |
rs777643075 | snp | G/T | 4.96874e-05 | 0.0049841 | intron-variant | BTRC | GRCh38.p7 | 10:101462079 | AAATTCAGCCTTACT[G/T]AAAATAAAAAGCTAC | 8945 |
rs777663254 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423510 | AGTACATTGTTAAAT[A/T]TTTTCTTGTAGTTAC | 8945 |
rs777672744 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101499368 | AGCCGGGATTATAGG[C/T]ATGCACCACCATGCC | 8945 |
rs777674405 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101532972 | GGATAAAAACACATT[A/G]GAATGCAAGCGAATT | 8945 |
rs777685827 | in-del | -/TCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101411544 | CCTCGGGTTCACTGA[-/TCT]TCTACAGAGTTTAAA | 8945 |
rs777726932 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101551428 | CTCCAAAAAGAGGAC[C/T]TGTCTTTTGACCTCT | 8945 |
rs777754255 | snp | A/C | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353310 | AAAGAAAATATTTAT[A/C]TGCTTTATTTGCTGG | 8945 |
rs777768870 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101418692 | GTATAATTGGCAAAC[-/AA]AAATTATTATTATTA | 8945 |
rs777778843 | snp | C/T | 1.66871e-05 | 0.00288847 | intron-variant | BTRC | GRCh38.p7 | 10:101550677 | GTTCAAGTTCCTACC[C/T]TTTTTGTTTCTACTT | 8945 |
rs777780592 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101476342 | GAAAAACTGGTGAAA[A/C]CTGAGTAAGTTCTGT | 8945 |
rs777811818 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101370736 | CCAAACATCGGCTAA[-/T]TTTTTTTGCATTTTT | 8945 |
rs777814350 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101402459 | TTATTTTAGAAGGCA[C/T]CCAAATTTTAACAAT | 8945 |
rs777825666 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415968 | GCTTGTAGCACAGGA[A/G]CAATATGCTCTACCT | 8945 |
rs777830197 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471416 | GACAGATAGATAACT[A/G]CTTTTTTTTTCATCT | 8945 |
rs777843709 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101366362 | AAAGTTGAATAAAAC[-/T]TCTCTAGAGCTTCAC | 8945 |
rs777851060 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507449 | GTGCCGCTCCGATCC[A/G]GGGAAATGATGATCC | 8945 |
rs777854047 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392783 | CCTGCCTCGGCCTCC[C/T]AAAGTGCTGGAATTA | 8945 |
rs777860504 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445703 | TGTGTATAATCGCTT[C/T]GGTTTAATCAATAGA | 8945 |
rs777911710 | snp | A/C | 1.73963e-05 | 0.00294921 | intron-variant | BTRC | GRCh38.p7 | 10:101532456 | TATTCAGTTGTAGAA[A/C]GGTAGCAGAGGGAGC | 8945 |
rs777960587 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101545225 | TCATTAGTTTTCAGC[-/A]ATTTGCTTATGATGT | 8945 |
rs777971800 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101386729 | AAGTCCAAGTCTAGT[A/T]GGTGCTTTTCCGAGT | 8945 |
rs777981462 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417434 | CAAATTAGGTATCTT[C/T]GACAGGAATATCACA | 8945 |
rs777995345 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101526294 | AATGAGACCACTTCT[C/T]ATTTAATATGGTGAT | 8945 |
rs778010209 | snp | C/T | 1.68318e-05 | 0.00290096 | intron-variant | BTRC | GRCh38.p7 | 10:101535331 | GCACCAAATCAACTG[C/T]TCAATGCCATTTTCT | 8945 |
rs778011974 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101493739 | GCATTCCATATGAGA[A/T]GATAAAAATTAAAAA | 8945 |
rs778039161 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101538234 | ATTTCTGCTATTCTT[C/T]CCTGCCTTCTCTTAC | 8945 |
rs778085949 | in-del | -/GAG | | | intron-variant | BTRC | GRCh38.p7 | 10:101493909 | TTGGATGCCACAAAA[-/GAG]AGTGAAGTGGAGAAA | 8945 |
rs778102018 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506215 | ACCTGTAGTTTTCGC[A/G]CCTGGCTAGTTTTCC | 8945 |
rs778106273 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101454705 | GAGGATTACTTGAGC[C/T]CAGGAGTTGGAGGTT | 8945 |
rs778155106 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358790 | GCCAGTCTTCTAAAT[C/G]CTAGATTTGGAAGTC | 8945 |
rs778157120 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101495108 | ACCAAAGAGCAGGGT[C/T]CTCCTAATACTGACC | 8945 |
rs778159101 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534872 | GTAGACTTTGATGAC[A/G]AGTACATTGTTTCTG | 8945 |
rs778165516 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101523422 | GTCAGTATTTGGGGG[A/G]AATGCTATTTCAGGA | 8945 |
rs778188855 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543596 | TTTGCTTTTGTTTGT[C/T]ACCTCCTGTTTTCAT | 8945 |
rs778198946 | in-del | -/GCT | | | intron-variant | BTRC | GRCh38.p7 | 10:101385158 | GGCTATGATTCCTCC[-/GCT]GCATTCCAGCCTGGG | 8945 |
rs778227544 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101481233 | ACAAGCGTGAGCCAC[C/T]GCACCCAGCCCAAGT | 8945 |
rs778232182 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101449702 | CTTGGCTTTTTATTA[C/T]GTATGTCTTTCTATC | 8945 |
rs778286699 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101380339 | TAAGCATCCAGATCA[-/T]TGTGTCTCTTAAAGA | 8945 |
rs778322158 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101427301 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 8945 |
rs778338558 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101518232 | AGTGTCTTAATTGGC[A/C]TCCTTCTATTTATGT | 8945 |
rs778342968 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101516832 | AGCTGCTGATTGTTC[C/T]TCTCTGTTACTGGCA | 8945 |
rs778359611 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101354965 | TTACAAATGTCAGGG[A/G]GGGGTACATAACGCT | 8945 |
rs778359952 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370158 | GGTCTCACTCTTTTG[C/G]CCAGGCTGCAGTGCA | 8945 |
rs778380619 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101395093 | CCTAGGATCTACTGG[C/T]TTCAGCTAATGTAGA | 8945 |
rs778399338 | snp | C/T | 8.83072e-05 | 0.00664423 | intron-variant | BTRC | GRCh38.p7 | 10:101535505 | TGTATCATAAGGGAT[C/T]AATATTATGCTCCCA | 8945 |
rs778406203 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101388431 | TCTTGGCCTGAAACA[A/G]TCTTCCTGCTGTGGC | 8945 |
rs778418342 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101485709 | TATATCTGACTGAGG[C/T]ACTTCAAGATGCTAG | 8945 |
rs778419530 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101513485 | ACTGATCTGTTTTTC[C/T]AACAATTAGAATTAC | 8945 |
rs778458259 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101464224 | TAATAGGCTGATCCA[A/G]ATGGTCCATTTGGAA | 8945 |
rs778464863 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434862 | CTGTTCTTAAACTCC[G/T]GTCTTCAGGTGATCT | 8945 |
rs778484772 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369115 | GTTTCCTTAATGACT[A/G]CTGTAAACAAGCACC | 8945 |
rs778499244 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101380361 | TCTTAAAGATGAATT[A/C]GATTTAACAACCTCT | 8945 |
rs778519752 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101377457 | TTTTTAGAAATTGCT[A/G]TTTTCCAGAGTGATT | 8945 |
rs778520224 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474602 | AGTCTTCCTCCTTCC[C/G]CTGTGGTTCTCTTTC | 8945 |
rs778523057 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101410356 | GCAGGGTGGCTCACA[C/T]CTGTAATTCCAGCAC | 8945 |
rs778529975 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525851 | AAATTATTGACACTC[A/G]TTTTACCCAAGCCTC | 8945 |
rs778534600 | snp | A/C | 1.73024e-05 | 0.00294124 | intron-variant | BTRC | GRCh38.p7 | 10:101532446 | AGGTGAGGTCTATTC[A/C]GTTGTAGAAAGGTAG | 8945 |
rs778540101 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101397097 | GCATGAGCCACTGCG[C/G]CCAGCCTGTCCAAAA | 8945 |
rs778548453 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101541662 | GTTGGATTTTGTGAA[A/C]TGCTTTATCTACATC | 8945 |
rs778573734 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101359355 | TTTAAATTGGCTTTC[-/A]AACAGTTTGTTTTCT | 8945 |
rs778580908 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515181 | GGCTGGTCTCAAACT[C/T]CTGACTTCAAGTGAT | 8945 |
rs778584706 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101501229 | AAACGCCAATATGAT[A/G]GGTTTTAAGTAAGAA | 8945 |
rs778603877 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101456120 | AAGTTGTAATGAGCC[A/G]AGGTCGCCACTGTCC | 8945 |
rs778616846 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101543761 | TATTGTACCACTTCA[C/T]GTATAATGTAGGAAA | 8945 |
rs778633255 | snp | A/G | | | downstream-variant-500B | BTRC | GRCh38.p7 | 10:101557661 | ATCAGTTTATAGGCA[A/G]GCAAGCTCACATCTG | 8945 |
rs778653912 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451213 | GAAAACAAAATTCGT[A/G]TAATCAGGTTGATGT | 8945 |
rs778658969 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101381363 | ACATTCTAGCTCCAG[A/G]GTGAGTGTGGTTAAT | 8945 |
rs778659041 | snp | A/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101352051 | AATCACCAAAAATGC[A/T]GTTACCTTTGCCTGG | 8945 |
rs778681871 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101459302 | AGGCTTTGAGAACTG[C/T]TGAGGTGACTACTTA | 8945 |
rs778691136 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101488804 | ATGCAAAAGCTGGTT[A/G]CCAGGTACCCACCTG | 8945 |
rs778718834 | snp | G/T | | | | | GRCh38.p7 | 10:101458538 | GGAAATTAATATTGA[G/T]ACAGTGTTATTAGTT | 8945 |
rs778746064 | snp | C/T | | | | | GRCh38.p7 | 10:101502567 | TAAATTTTTGCATAC[C/T]AATCTTAGAAAATGG | 8945 |
rs778751430 | snp | G/T | | | | | GRCh38.p7 | 10:101500728 | TTTTAAATTATTAAT[G/T]TTAAAGTCAGCATGT | 8945 |
rs778752998 | in-del | -/GTT | | | | | GRCh38.p7 | 10:101416547 | CAATTGAAAGCCTGA[-/GTT]GTTGTTGTTGTTATT | 8945 |
rs778758925 | snp | C/G | | | | | GRCh38.p7 | 10:101513662 | GCAGCATCACAGTTT[C/G]TTTACCAGTTAATCT | 8945 |
rs778772433 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101473552 | CTCAGCTTACTGCAA[A/C]CTCCGTCTCCCGGGT | 8945 |
rs778784269 | snp | A/G | 1.64909e-05 | 0.00287144 | intron-variant | BTRC | GRCh38.p7 | 10:101532945 | AGGATCTTATTTGCC[A/G]TCCTAGATCTGGGAT | 8945 |
rs778786174 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101365679 | ACAGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 8945 |
rs778814755 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366021 | TTAGGGTCTCTCTCT[A/G]TTTTTCCTTTCAGTT | 8945 |
rs778814967 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101435937 | AAAATTCTTATGGCA[A/G]TAAAGAAGGAGAAGC | 8945 |
rs778856169 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101503676 | GTGCTGCTGCCTCAT[-/A]GAATTATTTCTTGCT | 8945 |
rs778864948 | snp | A/T | 1.68156e-05 | 0.00289957 | intron-variant | BTRC | GRCh38.p7 | 10:101430326 | ACTGTCCCATCTCAT[A/T]GTTGTCCTCTCTCTG | 8945 |
rs778895314 | in-del | -/AC | 4.9525e-05 | 0.00497595 | intron-variant | BTRC | GRCh38.p7 | 10:101536666 | TGGGTGAGTGTGCTA[-/AC]AGAGTGTAAAAAAGA | 8945 |
rs778902038 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446026 | ATTTGCTGGGTCACT[G/T]CTTTGAATGTCTTAT | 8945 |
rs778932961 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101521483 | ATTTACCAACTTTCT[A/G]TGGTATTTCTGTGGT | 8945 |
rs778954524 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407011 | CAATAGAAACATTTA[C/T]CACAGATGCCAACCA | 8945 |
rs778965331 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101471974 | CATGCCCCCTTTGAC[G/T]TATCTTCATCGTTCT | 8945 |
rs778981071 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101552022 | ATATACCTACCCCCT[C/T]CTTTGCCCAAAATTT | 8945 |
rs778989218 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101430920 | TATACTACTAAGTAT[A/G]TATTTTTTATAACTG | 8945 |
rs779007184 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101484033 | TAAAATTGAATTGTT[C/T]GAATACATCTATCCA | 8945 |
rs779007541 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101405126 | TGAGTTCCTCCCTCT[C/G]TACAATCTCCCCAGT | 8945 |
rs779024841 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101445225 | ATGGTGTTTTAGGAC[A/T]TTGGAATAGCTGATT | 8945 |
rs779027538 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101392719 | AGTAGAGACAGGGTT[G/T]CACCATGTTGGCCAG | 8945 |
rs779070066 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101550139 | CCCTACGCCAAAAAG[G/T]GTTGGCCATGAGAAA | 8945 |
rs779071900 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445550 | TGAAACTAAGAATCA[A/G]CTCTTCAGTGTATGG | 8945 |
rs779086863 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101535793 | TAATTTTTGTCTTAG[C/T]ATTACATAATTGGCC | 8945 |
rs779090620 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101438043 | TGACATGAAGAAAAG[A/G]AGTATTCATTTTCGT | 8945 |
rs779101299 | in-del | -/TAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101363176 | GTGAGATAGATTCAG[-/TAT]TATTATTATCCCCAT | 8945 |
rs779102878 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546032 | TGTTATAGTTGGAGA[C/T]TTCAGCACCCCCTAT | 8945 |
rs779109549 | in-del | -/TACCCACACCCACAGA | | | intron-variant | BTRC | GRCh38.p7 | 10:101483984 | TCCCTAATTTACCCT[-/TACCCACACCCACAGA]TACACAAATACATGC | 8945 |
rs779119865 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101538315 | AAAGTGTGGGATCTT[A/G]TGGCTGCTTTGGACC | 8945 |
rs779126209 | in-del | -/A | 8.4122e-05 | 0.0064849 | intron-variant | BTRC | GRCh38.p7 | 10:101531371 | GTATTGCCCAAGGGC[-/A]CAGAATTATCAGCAT | 8945 |
rs779131917 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101431226 | GGATTACAGTTACGC[A/G]CCACCACGCCTGGCT | 8945 |
rs779144769 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101483320 | CTAAAAATGGCCGGG[A/C]ACGGTGGCTCACACC | 8945 |
rs779181400 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398723 | TTTATATTTGATGTT[C/T]CTGTGTTGTGGTTGA | 8945 |
rs779187266 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101415637 | ACCTCTGCCTCCTGA[A/G]TTCAAGCGATTCTCC | 8945 |
rs779220657 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101414167 | CAACCACCATCCTAC[C/T]TTCTGAATTTGACTA | 8945 |
rs779262762 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101460926 | TTGTTGTTTTGAGAC[A/G]GAACCTTGCTCTGTC | 8945 |
rs779263072 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534852 | ACCGAGCTGCTGTCA[A/G]TGTTGTAGACTTTGA | 8945 |
rs779269756 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385292 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 8945 |
rs779276470 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360888 | TGAGCTCCCTGCAGC[C/G]TCAAACTCCTGGGCT | 8945 |
rs779327428 | snp | A/G | 0.000110736 | 0.00744014 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354138 | CGGCCTGGCACCAAA[A/G]GGGCGGCCCCGGCGG | 8945 |
rs779359565 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101454256 | TTCCCAGTAATCTTT[C/G]AATCTTACTGGTTAG | 8945 |
rs779381575 | snp | C/G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101461700 | AGTGTCAACCTGTGT[C/G/T]AAAGTGCAAGCTAGA | 8945 |
rs779417396 | in-del | -/AAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101523210 | TCCATCTCAGAAAAT[-/AAAT]AAATAAATAAATAAA | 8945 |
rs779421108 | snp | C/T | 1.77543e-05 | 0.0029794 | intron-variant | BTRC | GRCh38.p7 | 10:101414631 | TAGGAGATGACAGGT[C/T]CATAGATGTTAATTG | 8945 |
rs779428889 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101425446 | TGGGAACTGAGCTGA[A/G]GAAACTAATATGTGC | 8945 |
rs779431034 | snp | G/T | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101534892 | CATTGTTTCTGCATC[G/T]GGGGATAGAACTATA | 8945 |
rs779459440 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101434144 | CATGTCTGCTTCTGC[A/T]CTCAATCTATTGTGG | 8945 |
rs779460851 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101476975 | GATGGAAACCTAGCA[A/G]TCTGTGTTTGTTTTG | 8945 |
rs779471252 | in-del | -/AAAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101508914 | GCAAGACTCCATCTT[-/AAAAA]AAAAAAAAAAAAAAA | 8945 |
rs779480356 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101403426 | TATATTCCTTTTTCT[A/G]TGTTGCTGGATTTTA | 8945 |
rs779487658 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101547111 | TTCAATAGGTTAGGC[A/G]GATCAAATGCATTTT | 8945 |
rs779535637 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101408634 | AAAAAATTTTCCTGC[C/T]TTCTTTTGGATTTAT | 8945 |
rs779554704 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101529989 | ACTAGCTTCCACACC[A/G]TGTTTGGTGGGTTCT | 8945 |
rs779555109 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101436292 | TAGCTGAGTAATTAA[C/G]ATTCTTTATTTTGCT | 8945 |
rs779555626 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512909 | TAGTGTTACCATTAA[C/G]CTGAGGCTGTTTGTC | 8945 |
rs779607794 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101493452 | ATGTTGCAGAACTGG[A/C]ATTTGAACCCAGACC | 8945 |
rs779634724 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101540272 | TTTGTATTTTGGTCT[A/G]TGATCCATTTTGAGT | 8945 |
rs779642792 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101354664 | GGGAGCGCGGGATAG[A/G]GTGAAGACAGATACG | 8945 |
rs779643253 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101394945 | ACCAAGAATGCTAGG[A/G]CATGCATGCACAGAT | 8945 |
rs779644017 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101463466 | ATTACAGACATGAGC[C/T]ACCACACCTGGCCCT | 8945 |
rs779663815 | in-del | -/AC | | | intron-variant | BTRC | GRCh38.p7 | 10:101418257 | CCTGTAGTCCCAGCT[-/AC]TCAGGAGGCTGAGGC | 8945 |
rs779664856 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556493 | AGTCTGTAGCAGAGC[A/G]GTCCAACCCAGATTA | 8945 |
rs779666538 | snp | A/G | 9.88728e-05 | 0.00703041 | intron-variant | BTRC | GRCh38.p7 | 10:101538264 | CATTTGCTTTTAACT[A/G]ACATTTTTGTCCCCT | 8945 |
rs779667946 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424601 | TGTCATTCAGCTTTC[A/G]TATAGTAAATGCTGA | 8945 |
rs779681361 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555154 | ATTGGGTAAGGATTT[C/T]GCTATAGATGAAGGT | 8945 |
rs779688740 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101556602 | AACCACAGTGTCAAC[A/G]TAGTATCGGAAAGAG | 8945 |
rs779690203 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369075 | CTGTAGTGGATGATG[A/G]TACTATCCCACCGTT | 8945 |
rs779696463 | snp | C/T | 1.77521e-05 | 0.00297921 | intron-variant | BTRC | GRCh38.p7 | 10:101414648 | ATAGATGTTAATTGC[C/T]CCCAAAGACCTTCCA | 8945 |
rs779697471 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101410223 | GATGGCTGCTTTTTA[A/G]CTTTCTTTAGTTCTT | 8945 |
rs779702860 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101356214 | ACTATGTTGGCCAGG[A/C]TGGTCTCATCTCCTG | 8945 |
rs779712776 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101517909 | TGTTGAAGTAGTGTC[-/T]TTTTTTTTTTTTTTT | 8945 |
rs779748429 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101483001 | GGCTTGGCTAGAGAT[A/G]CTAATTATAGGCCAA | 8945 |
rs779753566 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358299 | GTAGAGACAAGGGTC[A/G]CCCTTTGTTGACAGG | 8945 |
rs779757259 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515344 | GAGTTAATTTGCCTG[C/T]TGAGACTTTGATATT | 8945 |
rs779757401 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101531171 | GCGAGACTCTGTCTC[A/G]AAATATATATGTATT | 8945 |
rs779794566 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509809 | TCAAGCAGTCCTTCT[G/T]CCCTGGCGTCCCAAA | 8945 |
rs779806157 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407728 | ATTTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTGT | 8945 |
rs779822932 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101447569 | TAAAATTAATGTTTG[A/G]TATCTGTCAAACCAA | 8945 |
rs779833243 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101479922 | CTTGATCCACATGGA[C/T]AAGTATGTTTAGTCA | 8945 |
rs779854367 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101510971 | CTTTTGCAACTTGCT[C/G]TTATTATCCCCTCCC | 8945 |
rs779874929 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525767 | TTGGGGGGTTTGCTG[A/G]TTGTTAGCTTTAACT | 8945 |
rs779896199 | snp | A/G | 3.42384e-05 | 0.00413739 | intron-variant | BTRC | GRCh38.p7 | 10:101430299 | CCTGTAATCTGTGCC[A/G]TCCTGTCTCATACTG | 8945 |
rs779904962 | snp | G/T | 1.6489e-05 | 0.00287128 | intron-variant | BTRC | GRCh38.p7 | 10:101538409 | AGCATTGGAGAGCAG[G/T]TGGGGGAAGAAATTA | 8945 |
rs779905340 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101487461 | CATCAATAAACTGCA[C/G]TGCCTCTAATAAAGC | 8945 |
rs779915641 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101380165 | GGTTCTGCTTCCTAG[A/G]TGTCATAGATATTGG | 8945 |
rs779930397 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101396194 | TCTTTGCTCTCATTT[C/T]CCAACATGATGGACC | 8945 |
rs779943076 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101473287 | AAGCCTCTCCAGTAA[A/G]TTTTTTGATTTTTTT | 8945 |
rs779993410 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101378523 | CTCCCAATTATAATT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs779996180 | in-del | -/TCGTATAAATAAAGATGGGCAGGGC | | | intron-variant | BTRC | GRCh38.p7 | 10:101373614 | GAATTTAAGATATAT[-/TCGTATAAATAAAGATGGGCAGGGC]CGGGCGCGGTGGTTC | 8945 |
rs780004511 | snp | A/G | 0.000134472 | 0.00819865 | intron-variant | BTRC | GRCh38.p7 | 10:101531369 | GGGTATTGCCCAAGG[A/G]CACAGAATTATCAGC | 8945 |
rs780031098 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449489 | AATTTACACAAAACT[A/G]TATGCAGAGGATCTC | 8945 |
rs780032919 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101526864 | TGTTTCTTCTTAAGA[C/G]TTCTGTTTTTCAAGA | 8945 |
rs780042842 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360656 | GATTATAGGCATTAG[C/G]TACCGCGTCTGGCCT | 8945 |
rs780053594 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433244 | TGAATACTTTACATA[C/T]ATATATAGATGTTTA | 8945 |
rs780096059 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101362733 | TAATACAGTCAGCCA[C/T]GAATAGCTAACAGCT | 8945 |
rs780115513 | snp | G/T | 1.64882e-05 | 0.00287121 | splice-donor-variant | BTRC | GRCh38.p7 | 10:101536655 | GGGGCCTATGATGGG[G/T]GAGTGTGCTAACAGA | 8945 |
rs780121202 | snp | C/T | 3.31082e-05 | 0.00406854 | intron-variant | BTRC | GRCh38.p7 | 10:101533108 | TTGAACTCTGAAATA[C/T]CAGCTCTGCTCTGTT | 8945 |
rs780124668 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101443554 | GCATTTAAAACGATC[A/G]CTTTCCATTTGATCA | 8945 |
rs780133712 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101535562 | AGTCTTCAATTTTGT[G/T]ATGTTTATAATCAAC | 8945 |
rs780139307 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101551141 | AGTCATTCCTGCCCT[A/G]GTTATCTAGTAGTAC | 8945 |
rs780171727 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101404774 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 8945 |
rs780172291 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101445071 | TAGGGTTTAGTTATC[A/G]ACATTTCATTTGAAG | 8945 |
rs780175224 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101458389 | AATTTCAAGAGAATT[G/T]TGGGAGTGGTGGAAT | 8945 |
rs780198232 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479437 | AGCACTGCTATGAAG[A/G]CTGAGAATTGTGTGG | 8945 |
rs780226458 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101451630 | CAAGTGTTTGCCTGC[A/G]TAGACAATATATTTT | 8945 |
rs780235219 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101512279 | TTAATCATTATATCC[C/T]CTTTCCCCCCATAGT | 8945 |
rs780244272 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101497274 | GTTACTCTTCAAGAT[C/T]ATCTTGGTTATTCTT | 8945 |
rs780253067 | snp | C/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101406039 | GGCTCTCAAACTATG[C/T]AGATTTGTGTATTTT | 8945 |
rs780254951 | in-del | -/AA | | | intron-variant | BTRC | GRCh38.p7 | 10:101480809 | TCAGTTAAATGTCTC[-/AA]ATCCAAATATGTTAA | 8945 |
rs780257010 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101358080 | TAAGATAGGGGTTGA[A/G]AAGACATACTGAGGA | 8945 |
rs780296306 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471568 | TTGCCAGGTTTTGGT[A/G]TCAGAGTTATGCTGG | 8945 |
rs780322092 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101420243 | ACCTAGCTCTTATTA[C/T]CCTTTGTATTTGATC | 8945 |
rs780332578 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101429216 | TTAGACTGTAATAGC[A/C]CTCAAGTTGATGGAT | 8945 |
rs780334598 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101399515 | AAAGGAGTTCAAAAT[-/G]AAAGACTGTCAGTAC | 8945 |
rs780335411 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101533714 | ACTTTAAAAAAAAAA[C/T]AGACCTAGGAAAAAA | 8945 |
rs780335458 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101391200 | CCCTTAAGCAGTTAT[A/G]TTAGGCTTGGGGAAT | 8945 |
rs780351352 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101466011 | CCACTGTTTTCCTAC[C/T]TTTTATTCCTATCTG | 8945 |
rs780354537 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101546920 | AGGCAGATCCACTGG[-/T]GAATTCTACCAAACA | 8945 |
rs780355910 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427566 | AGGGTCTTGCTTTGT[C/T]GCCCAGGCTGGTGTG | 8945 |
rs780369115 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101437519 | TTTAATATTCATTGT[A/C]GAAAATAGAAGTAGA | 8945 |
rs780409098 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101467786 | CTTAATTTTAGTCAT[C/G]TGTTTTAATTACCTA | 8945 |
rs780444305 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101520157 | TGTTTGTTTGTTTGT[C/T]TGGGGGGACAGAGTC | 8945 |
rs780465597 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101519162 | CTCCTCACTGCAATC[C/T]CCACCTCCTGGGTTC | 8945 |
rs780492581 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101441958 | ACACAATTTAAATAA[G/T]GTAATTTAATTACTG | 8945 |
rs780528049 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506097 | TTTTCTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 8945 |
rs780530209 | in-del | -/TGT | | | intron-variant | BTRC | GRCh38.p7 | 10:101527760 | CCCTGTCTCTTTCTC[-/TGT]CTCTCTCTCTCTCTC | 8945 |
rs780535096 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383689 | TTTCTACTTGTTTGC[C/T]TTCTTTAATAGATAT | 8945 |
rs780565496 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101413830 | TGTTTTTTTATATAC[A/C]GGATTTTCATGTTAT | 8945 |
rs780578816 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452959 | ACCTAAGTTTTCCCC[A/G]TTGTATCCTAAAAGG | 8945 |
rs780579198 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101526157 | TCGAGAGAATGGTCA[C/G]GACAGATTCTCTGTG | 8945 |
rs780598947 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101490363 | CCCAGTGTTCAGGCA[C/T]TATATAGTGCTAGCT | 8945 |
rs780613908 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101438894 | TCTCTTTTGTATTCC[C/T]TACTCTGGTTCAATT | 8945 |
rs780615960 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101423785 | GGTAAACTTTACTTA[G/T]CCTCTTTTTGTACTC | 8945 |
rs780616578 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412165 | ACTGTATGTATACAG[A/G]ACTTAGTATTCAGGA | 8945 |
rs780619185 | snp | A/C/T | 5.32603e-05 | 0.00516021 | intron-variant | BTRC | GRCh38.p7 | 10:101414642 | AGGTCCATAGATGTT[A/C/T]ATTGCTCCCAAAGAC | 8945 |
rs780632847 | snp | A/G | 1.67413e-05 | 0.00289316 | intron-variant | BTRC | GRCh38.p7 | 10:101550897 | ACTTGCCCAGGTATC[A/G]AAATCGATTATGTAC | 8945 |
rs780634752 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101483788 | AATGGACAGTCATTA[C/T]TAACTGTCAACTTAG | 8945 |
rs780650069 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101486287 | GACTTGTAATAACGT[C/T]GGCAAGAGTCCGCAT | 8945 |
rs780667745 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101400586 | GAAGGGTTTGCCTCC[A/T]CTCCCTGTCAAAGGA | 8945 |
rs780693998 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101381176 | TAGCTCAGTATATAC[C/T]GTGCAGGATTCTAGA | 8945 |
rs780700276 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101417362 | AGGATTACACGCCAG[C/T]ATCTTGCAGAACATT | 8945 |
rs780717772 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101366180 | CATTTTCTGTTAAGT[A/G]GTACTTGGCAATAAA | 8945 |
rs780733461 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101407445 | TTTGGAAACAGTCTC[A/G]CTTTGTTGCCCAGGC | 8945 |
rs780738789 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101437935 | TCAAGCTGAGCTAGA[A/G]TTAAAGTCTTCCCTG | 8945 |
rs780750537 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101465165 | AAAGATGTCAAGGCC[A/G]CCTTATACCTAGTAT | 8945 |
rs780752875 | snp | C/T | | | upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101353335 | TGCTGGAGGCCATTA[C/T]ATTCCACCGTTGAAG | 8945 |
rs780762523 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474941 | GCCATTACTGGAAGC[A/G]GAACTCTTTGAGTCA | 8945 |
rs780811166 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101369216 | CCCTATTGGAGTATT[A/G]TTATTTTTTTTTTTT | 8945 |
rs780811245 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101500484 | ACTTTTTGCCTTCTT[A/C]TGAAGCAAAGGGATT | 8945 |
rs780813080 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555044 | TTTCTCAATGTAATT[C/G]CCTTCCCAGCTACCC | 8945 |
rs780822103 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101433917 | TTTGTTTATATGGCT[C/T]ATATCTATTGATATT | 8945 |
rs780846829 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101424491 | ATGGCTTAAGGATAC[A/G]TAAACTCTCAGTACA | 8945 |
rs780888285 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101528719 | AAAAAAAATTTACTC[C/T]ATCAGTTTCTCATTT | 8945 |
rs780893548 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101400079 | AAATTCCATAAACTG[A/G]ATGGGGAGGGTAGAT | 8945 |
rs780932091 | snp | A/G | 0.000327243 | 0.0127873 | utr-variant-5-prime, intron-variant, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101354154 | GGGCGGCCCCGGCGG[A/G]GAGCGGACCCAGTGG | 8945 |
rs780933295 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101506019 | TCCAGGATTCAAGCA[A/G]TTCTCCTGCCTCAGC | 8945 |
rs780962901 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101536797 | ATATTTCTTTAATCC[A/G]TGTATTTACCTCTCC | 8945 |
rs780973144 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101431544 | CTGAGTCTTATCTGC[A/G]TACCTCAGGTATTTG | 8945 |
rs780975986 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | BTRC | GRCh38.p7 | 10:101538245 | TCTTCCCTGCCTTCT[C/T]TTACATTTGCTTTTA | 8945 |
rs781001725 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101537103 | TACAGTTCTCTTGTC[A/G]TCACTTGTCATCCTA | 8945 |
rs781012778 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101529823 | TTAATTATATTGTAA[C/T]GGAGCTATAGAGGGA | 8945 |
rs781013262 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101433098 | AGGGGCCCAGAGACC[A/G]CTTTCCAGTAGCCAA | 8945 |
rs781015086 | in-del | -/ATAAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101505640 | AATAAAAAAAAAAAA[-/ATAAT]AATAAAAAAACAAAT | 8945 |
rs781043254 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555865 | GACAGGCTGAAACCC[C/T]TTCAAAGGCAGATGA | 8945 |
rs781081580 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101368470 | AACTGTTTTTCTTTT[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTTAGAGACAG | 8945 |
rs781085433 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101408528 | CCCAGGCTGGTCTCC[A/G]ACTCATGGACGCAAG | 8945 |
rs781135427 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101536627 | TCGATTTGATAACAA[A/G]AGGATAGTCAGTGGG | 8945 |
rs781145301 | in-del | -/AGG | 3.31978e-05 | 0.00407404 | intron-variant | BTRC | GRCh38.p7 | 10:101536695 | GAGAAAATCTACGTC[-/AGG]TTAATCCTTCCTTAT | 8945 |
rs781151619 | snp | G/T | 4.94678e-05 | 0.00497307 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101479416 | CAAGAAACAGTATGT[G/T]TAGCAAGCACTGCTA | 8945 |
rs781153169 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449029 | ATAATTTCTTAATTA[A/G]GAAAAAAAATAATGA | 8945 |
rs781156723 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101452575 | GTGTCGGACAGTGTG[A/G]CGGGGAGAAAGCCTG | 8945 |
rs781178684 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101455219 | CTATGCCCAGCTAAT[-/T]TTTTTTTTTTTTTTT | 8945 |
rs781189316 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101446635 | TGCTTTCTATATGGA[C/T]TAAAAAATTAGGCCA | 8945 |
rs781204911 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101533000 | ATTCTCACAGGCCAT[A/G]CAGGTTCAGTCCTCT | 8945 |
rs781231737 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101402667 | GAAATATCTTATTCT[A/G]TCCATTTTACCAGCA | 8945 |
rs781232162 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101361483 | ATGAAATAGAAAATA[C/T]TTACCAAAGTTTAAC | 8945 |
rs781249186 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101464352 | ATACAGATGGACCAG[-/C]AGGTCACACATGGGA | 8945 |
rs781289551 | snp | C/T | 1.65222e-05 | 0.00287417 | synonymous-codon, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550854 | ATACACCTACATCTC[C/T]AGATAAATAACCATA | 8945 |
rs781308933 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101497789 | CACTTTGGGAGGCCA[A/G]CGCGGGCATGTCACA | 8945 |
rs781316633 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471602 | TATAAAATGAATTGG[A/G]AAATCTTCCTCCCAT | 8945 |
rs781338954 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101389249 | TTTTCTTATGCCGAT[A/G]TGCAATTCACAAGAT | 8945 |
rs781339830 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101533154 | TAATTTTGTATATAT[C/T]GGCACAGTTCTGAAA | 8945 |
rs781381332 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101525447 | CATCTCTGTCTTTCT[C/T]TTGGGATATTTCCAT | 8945 |
rs781381945 | snp | A/C/G | 9.90416e-05 | 0.00703648 | missense, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101550847 | CTCGAACATACACCT[A/C/G]CATCTCCAGATAAAT | 8945 |
rs781410510 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101403672 | CATGGCTCACTGCAG[C/T]CTCGACCTCTCAGGC | 8945 |
rs781427499 | snp | C/T | 1.86142e-05 | 0.0030507 | intron-variant | BTRC | GRCh38.p7 | 10:101525988 | TTCTGTGTTCTTTTT[C/T]TTTGCCTCCTCCCCC | 8945 |
rs781444142 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101508184 | CTTTTCCTATAGTTA[G/T]TAAATAGGAAAAAAA | 8945 |
rs781462944 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101499953 | AGCTCTCTGCAATAC[A/G]GCAGGCTATGGACTA | 8945 |
rs781486277 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101362398 | TGCAGAGGTGCAAGA[A/C]ATTTTTTTTTTTTTG | 8945 |
rs781492156 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101464503 | AGGTTCTCTTCCCCA[C/G]TCCCCCTGCCCACTT | 8945 |
rs781495081 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516484 | TGTTAATGGATCTCA[A/G]GTATGTGTCTTTCTG | 8945 |
rs781506323 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441341 | ACCTTCACAATTAAT[A/G]ATTAGCTTTATTATT | 8945 |
rs781516126 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101493980 | TTTAGCCCTGTCGGT[C/G]TTGTTCTAGTTCATG | 8945 |
rs781571595 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101482867 | AACTTGGTACAAGTG[C/T]CTGTTGTTGATTCAG | 8945 |
rs781574267 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101360453 | ATCTCAACTCACTGC[A/T]ACCTCCGCTTCCCAG | 8945 |
rs781578184 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101533299 | ATTCTATTTTAATTT[C/G]GAGGATCATCTATTA | 8945 |
rs781585857 | in-del | -/CTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101383964 | AAGTGATTCTTCCGT[-/CTC]AGCCTCCCAAATAGT | 8945 |
rs781593398 | in-del | -/AT | | | intron-variant | BTRC | GRCh38.p7 | 10:101402764 | CTGTTCCACAACCTG[-/AT]ATGTCATGCCTTCTC | 8945 |
rs781599857 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543776 | TGTATAATGTAGGAA[A/G]CTTAAAACACTATAT | 8945 |
rs781605780 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101510757 | AGTATTATACTAAAA[G/T]AAATGTATATTATGA | 8945 |
rs781611008 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101465273 | ATTGATTATAAAAAG[-/T]TCAGTTATCTTCTAG | 8945 |
rs781639007 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101450127 | TTCTGATGTGGAGCA[C/T]ATTAGCATAATTACA | 8945 |
rs781644333 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101467174 | ACATTTCTTTTTTCA[A/G]GAGAGCTCCTTTTCT | 8945 |
rs781675223 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357754 | ATCCTGTTAATAAGA[C/T]TGCTGATTCAGAGAT | 8945 |
rs781680222 | in-del | -/GTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101456107 | ACCCAGGAGGCAGAA[-/GTT]GTAATGAGCCGAGGT | 8945 |
rs781710514 | snp | C/T | 1.66693e-05 | 0.00288693 | intron-variant | BTRC | GRCh38.p7 | 10:101535346 | CTCAATGCCATTTTC[C/T]TTTTCAGGTATGGAA | 8945 |
rs781723429 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101426030 | CTGACCAATCAGAAT[A/G]GCCCTGAAATGTATA | 8945 |
rs781748938 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101413560 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 8945 |
rs781750093 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101372030 | TTGTTCTTTTTCTAT[A/T]GCAGGGTCATTTTTG | 8945 |
rs781763663 | in-del | -/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101441789 | GGGAGGCTAAGGCAC[-/G]CGAATCGCTTGAACC | 8945 |
rs781764455 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101411431 | TTTGAGACACCAGAT[A/G]TGCATGTGTTAGACC | 8945 |
rs796082531 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421201 | TTCTTTTGATGTACG[A/T]TATCTTCTCCATGGC | 8945 |
rs796108094 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101366829 | ATATATTAATATATA[-/TT]TATATATATTTATGT | 8945 |
rs796110097 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101545331 | GAAGGCTAAACTTAT[A/G]TTGTCTACAAGAAAG | 8945 |
rs796135809 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101399835 | TTATTTTCCTGGAAG[-/A]AAAAAAAATTAGGTA | 8945 |
rs796145158 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101464542 | CAACCTTCCCCCCCA[-/C]CCCCCCCATGGTGCT | 8945 |
rs796151007 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421762 | TTGCTGAGAATGATG[A/G]TTTCCAGCTTCATCC | 8945 |
rs796155309 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101440235 | ACATCTTTTTTTTCA[A/T]GCTATGAGTAGGAGT | 8945 |
rs796159114 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101470329 | TACCAATTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 8945 |
rs796175972 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101531727 | CTCCATCAAAAAAAA[-/A]GAAAAGGAAAAGAAA | 8945 |
rs796180753 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505136 | ATATATGTGTATATA[C/T]ATGTATATATATATG | 8945 |
rs796205653 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357786 | ACCATAATTCACACG[C/T]GATCGAGACTTAAAG | 8945 |
rs796215935 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101473207 | TTCAGTTTATCTATC[-/T]TTTTTTTTTTTCGGT | 8945 |
rs796219904 | snp | G/T | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101515715 | ACGAGGTTTCACCTT[G/T]TTAGCCAGGATGGTC | 8945 |
rs796222925 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101507302 | AACATAAACACAGCG[C/T]TCATTTCTGGCAGGT | 8945 |
rs796226938 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | BTRC | GRCh38.p7 | 10:101438423 | GAGCGAGACTGCCTC[-/AAAAAAAAAAAAAAAAA]AAAAAAAAAAAGTCT | 8945 |
rs796232976 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101371174 | CTATTCTTTTTTTTT[-/T]GTTTGTTTGGTGTTT | 8945 |
rs796251122 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101364185 | TCTATTGTTGACACT[C/T]TCCTGATAGCACTTT | 8945 |
rs796251598 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101544425 | TTTTTTTTTTTTTTT[-/T]AAGGGATGGGGTCTC | 8945 |
rs796262093 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101398166 | CTTCTAGTAAAGATG[C/T]ATTAAGTGGTTTAAG | 8945 |
rs796279338 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101437933 | GCTCAAGCTGAGCTA[G/T]AATTAAAGTCTTCCC | 8945 |
rs796299532 | snp | A/G | | | intron-variant, upstream-variant-2KB | BTRC | GRCh38.p7 | 10:101514301 | GCCTATTCCAAGAAC[A/G]TCAAGGTTTTCTCCT | 8945 |
rs796320070 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463033 | CCACCATGCCTGGCT[A/G]ATTTTTGTATTTTGG | 8945 |
rs796350224 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101516083 | TTATGTTATACTTTA[A/G]TGAAAATTAAAATAG | 8945 |
rs796358602 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101507572 | TAGAAGCAGTTTTCT[C/G]CAATTCCCTAAGCTG | 8945 |
rs796363668 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101470774 | CTATGATCCATCTCA[A/G]ATTAATTCTTATACG | 8945 |
rs796366126 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427297 | TTATTTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 8945 |
rs796368251 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101449768 | TTGCGTATTTCTCTA[C/T]TTTGTACATTGTTGT | 8945 |
rs796384989 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101543971 | CTGGAGTGCACTGGC[A/G]TGATCTTGGCTCACT | 8945 |
rs796404078 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101509181 | ACTTATCTCTTTCCA[G/T]TCTAATCAAAGTGTA | 8945 |
rs796405043 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101505138 | ATATGTGTATATATA[C/T]GTATATATATATGTA | 8945 |
rs796422034 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101405268 | GAAAAAAAAAAAGCA[A/G]TGAGGTTTTGTCTCA | 8945 |
rs796449424 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101449351 | AGAATTTTGTCATAC[A/G]TCCTAAGGGTTCTAT | 8945 |
rs796496944 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101379902 | TATAAAAATACAATA[A/G]AGCCCTTTTTATAAG | 8945 |
rs796535126 | snp | A/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101426400 | TAATCGGGAATGCAT[A/C]CTCTGTGTGGTGTTT | 8945 |
rs796536532 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101369802 | GTTCGTTCGATAATT[G/T]CATAATTGTAACTCC | 8945 |
rs796552141 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101542863 | GCACCTGGCCTGCTT[C/T]ATGGTTTTTTTTGTT | 8945 |
rs796552602 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101471519 | GTGTCTGTTTCATGT[A/G]AGGTACTGGTTTGCA | 8945 |
rs796579545 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101357073 | GGTGGAGCTTGCAGT[A/G]AGCCAAGATCGCGCC | 8945 |
rs796595910 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101525704 | AGTGCTGAAATCCAT[A/G]TAGATAGATGTGAAT | 8945 |
rs796596144 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101427117 | CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 8945 |
rs796601911 | in-del | -/TT | | | intron-variant | BTRC | GRCh38.p7 | 10:101389107 | GTTGCATAATTGTGA[-/TT]TTTTGTGTGTGTTTT | 8945 |
rs796631104 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101456181 | TTCAAAAAAAAAAAA[-/A]GAATGATGATTGCCA | 8945 |
rs796643643 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101379572 | CATAATATACTACAT[A/T]TTTTTTTTTCCTAAG | 8945 |
rs796651018 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101479181 | TGTTCATGGGCACAT[C/G]AGTGGCTTTTGTAGC | 8945 |
rs796663938 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101412334 | GAGTTCCCCTTTCTT[A/G]TGCAGCAGCCTGGAC | 8945 |
rs796683562 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101377874 | AGTGACTTCAGAGCA[-/T]TTTTTTTTTTTTCTG | 8945 |
rs796685257 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101463959 | GCTTTAAAAAAAAAA[-/A]CAAACAAAAATCCAC | 8945 |
rs796686393 | in-del | -/TG | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101554405 | GTCAGGAGAAAACAC[-/TG]TTTTTGTTTTTTTTG | 8945 |
rs796696778 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101431817 | TTCATTTTTCCTTTA[C/T]AAAATTTAATATCTT | 8945 |
rs796703028 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101421770 | AATGATGGTTTCCAG[C/T]TTCATCCATGTCCCT | 8945 |
rs796706306 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101557259 | GGAGTGTGTTTTGGG[-/T]TTTTTTTTAACTGTT | 8945 |
rs796727785 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101555912 | GACCTTTTGGTGCAC[A/C]CTGGAGCTACTTGGA | 8945 |
rs796730110 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101425642 | TTTTTTTTTTTTTTT[-/T]AATTAAAAAAAATGT | 8945 |
rs796736037 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101385732 | CTTCCTCTTCCCAGA[C/G]ACACACACACACATA | 8945 |
rs796749944 | snp | G/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101389120 | GATTTTTTGTGTGTG[G/T]TTTTTTTTTTTTTTT | 8945 |
rs796757591 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101410692 | TTGCCCATTTTTTAA[A/T]TGAGTTGTCTTTTTT | 8945 |
rs796774221 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463711 | ATGGAGGGTTAGAGA[A/G]GTTAGATGACTTGTC | 8945 |
rs796779216 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BTRC | GRCh38.p7 | 10:101553497 | CCAGAATCTCTCTTG[A/C]TTTGCCATTAAGCAG | 8945 |
rs796789782 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101535856 | TTCACAGTTGGAAGT[C/T]CTTTTTGGGGTTTTC | 8945 |
rs796800055 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101385384 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAGT | 8945 |
rs796805096 | in-del | -/C | | | intron-variant | BTRC | GRCh38.p7 | 10:101429505 | CTCTTCCTCTCCCCT[-/C]CCCCCCTCCCCTCCC | 8945 |
rs796812533 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101532219 | AGCATTGAGCCATTG[A/G]TTGTCATTAAAGCCT | 8945 |
rs796812575 | snp | C/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101360790 | GTGCGTGCCACCACT[C/G]GCAGCCTAAAATACT | 8945 |
rs796819309 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101374800 | ATAAAAAAAAAAAAA[-/A]GAAAAGTTTATCCGC | 8945 |
rs796837740 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101422175 | ATTCTAACTGGCGTG[A/G]GATGGTATCTCATTG | 8945 |
rs796844724 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101503565 | TGTCTTCAGTCCCTT[A/G]ATGTTCCCAGGGTTA | 8945 |
rs796855250 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101421749 | TCCTTGTGATAGTTT[A/G]CTGAGAATGATGGTT | 8945 |
rs796866129 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101512695 | ATTCATGGTAATTTT[A/G]AAAGTGGTACGTGAA | 8945 |
rs796866926 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101370177 | GGCTGCAGTGCAGTG[A/G]CACAATCACAGCTCA | 8945 |
rs796869681 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101548012 | CTTTTCCTCAACTTC[A/G]TAAAGAAAAATGCAA | 8945 |
rs796903054 | in-del | -/ATTTC | | | intron-variant | BTRC | GRCh38.p7 | 10:101539524 | CTGATGTATATCAAT[-/ATTTC]ATTTCATTTCTTTTG | 8945 |
rs796903490 | in-del | -/ACTT | | | intron-variant | BTRC | GRCh38.p7 | 10:101491251 | TCAGGGTGGTGACTT[-/ACTT]TAGTAATTGTTTTAG | 8945 |
rs796904267 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101453104 | TAATAATTTCTGTTT[C/T]TGTAAATTGTAAATT | 8945 |
rs796933920 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101463208 | CCACTACCACACCGG[A/G]CTAATTTTTGTATTT | 8945 |
rs796938283 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101474334 | GCCCTTAGTCCTAAG[A/G]CATACTCTTGAATCT | 8945 |
rs796958776 | snp | C/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101357311 | CCAGGCCTGGTGGCG[C/T]GCACCTGTAGTCCCA | 8945 |
rs796960117 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101485006 | TTCTTCTAGATGTGC[A/G]TGCCGTTTAAGAAAA | 8945 |
rs796971731 | in-del | -/A | | | intron-variant | BTRC | GRCh38.p7 | 10:101415042 | TCTTAACCATTATAA[-/A]GTCTATAGTAGTGTA | 8945 |
rs796972528 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101383346 | AGGTGATGCTGCTGG[A/T]TCTGGGACTACACTT | 8945 |
rs796980406 | snp | A/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101492195 | TAATTTAATCCACAT[A/T]TTCTAGGAGTATCTA | 8945 |
rs796990417 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101373870 | TTGCAATGAGCCGAG[A/G]TCGTGCCACTGCACT | 8945 |
rs796990670 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101505171 | TGTATATATATATAT[A/G]TATATATTTTTTAGT | 8945 |
rs797012080 | in-del | -/T | | | intron-variant | BTRC | GRCh38.p7 | 10:101449609 | TAAAGAGGAAAGCAG[-/T]TTTTTAAAAGATTCC | 8945 |
rs797017565 | snp | A/G | | | intron-variant | BTRC | GRCh38.p7 | 10:101509276 | TTTTTTTTTTTTGAG[A/G]CAGAGTCTCGCTCTG | 8945 |
rs797021388 | in-del | -/TTTTTTGAT | | | intron-variant | BTRC | GRCh38.p7 | 10:101473288 | AGCCTCTCCAGTAAA[-/TTTTTTGAT]TTTTTTGAGATAGGG | 8945 |