SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs188057445 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80700132 | TGTCCAATATACATT[C/T]CTACAAACATCCTCT | 254065 |
rs188059466 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746695 | ACTGCATAAATAATA[C/T]AGTACAAAATGAAAA | 254065 |
rs188065328 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731627 | AGGCCGGGCGCAGTG[A/G]CTCACGCCTGTAATC | 254065 |
rs188066591 | snp | A/C | 4.57112e-05 | 0.00478053 | intron-variant | BRWD3 | GRCh38.p7 | X:80719679 | AGACCAGATACAAAG[A/C]CACAAAATTACTTAC | 254065 |
rs188067466 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80764066 | AAAATTTGCATAAAT[G/T]TTCTTAACTGATTTT | 254065 |
rs188068661 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80754771 | CAGCACTTTGAGAGG[C/T]TGAGGCAGGCAGATC | 254065 |
rs188074578 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80721832 | TAAATAGCTACCTCC[A/C]GCTGCGGGGTAGGGG | 254065 |
rs188083589 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80782804 | AGCTAATCAGGAAGC[C/T]GAGGCAGGAAGCTCA | 254065 |
rs188087612 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80804502 | CTCAGTCTCTCAAAG[C/T]GCTGGGATTACAGGC | 254065 |
rs188121902 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80787139 | AAAAACCATAAAATC[C/T]TTAGGGAAAATTTCC | 254065 |
rs188279670 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80760549 | ATTTGAAGTGTATGA[C/T]AGTCTAATGTGCACT | 254065 |
rs188283493 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785680 | TCTTTAAAGTGAGTC[A/G]CTAAAATCAAGATAT | 254065 |
rs188290431 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80769379 | TAAAAGAACACAAAT[C/T]ATAACAAACTGTCTC | 254065 |
rs188294529 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752489 | CCATACTATTTACCA[C/G]AGAGGCTGTACTTAT | 254065 |
rs188304765 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80704004 | AAATAACTACATACA[A/C]CAAGTCTTTAAATCA | 254065 |
rs188308914 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80788945 | AGGGGTTGAGCAAAC[A/G]ATACTGAGGCTGATA | 254065 |
rs188316178 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80680109 | TAAGCTACTTAATCT[C/T]GCATTAAAATGTATA | 254065 |
rs188340919 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738777 | ACTCCAGAGACAGGA[A/G]ACAGTTAAGAGCAAA | 254065 |
rs188389404 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726193 | GTATAACATATAACA[C/T]GTTTACATGTTATAT | 254065 |
rs188397681 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704606 | AAAGTCAATGTTACA[A/G]TTAAATATTTAAGTT | 254065 |
rs188399835 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80744793 | CTTAACAATTATCTA[C/T]TTATTAAAACATAGC | 254065 |
rs188422718 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80761698 | CATATTTAATTAGAA[C/T]AAATTTGAATTAGAT | 254065 |
rs188430201 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80777741 | ATAACTCTTGGGCAA[C/T]TTTATCTGTTACCTG | 254065 |
rs188436301 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80800218 | AATTCTGCATGGTAA[A/C]TAGTGCATAATATCT | 254065 |
rs188498975 | snp | C/T | 0.0157677 | 0.0873799 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669707 | GCCAATACAAATTAA[C/T]ATGTTGTTATACAAA | 254065 |
rs188504145 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80707791 | CCCTCTTAAATACAT[C/T]AGAAACATTGTTTTC | 254065 |
rs188533938 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80746010 | CTTTCTTGGTACGCT[A/G]TAGTCAAAGAGACTG | 254065 |
rs188540038 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80781498 | GTCCTGTCTCTCAGT[C/T]CCCCCTCTCAACAAG | 254065 |
rs188579253 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738410 | AACACGTAATTCTGC[C/G]ATTCAGTGGTAACCA | 254065 |
rs188622623 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763785 | CATGGATTGGAAAGT[C/T]TGACAGAGTAACATG | 254065 |
rs188632035 | snp | A/C | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675419 | ACTCACAGCTGTTAA[A/C]TGGTAAGTGGAGCAG | 254065 |
rs188636998 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80803318 | TGCTCAGGACAAAAT[G/T]TCATTAAGGCAAGTT | 254065 |
rs188771446 | snp | C/G | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80686017 | AAAAGTCCCTACAAA[C/G]GACATGAACTCATAA | 254065 |
rs188772883 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80697171 | TAATATATCTATTTT[A/G]GAAAAACTCCCTAGT | 254065 |
rs188803382 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729217 | TACTTATATTGGTTG[A/T]CAGAAAATATGAAAA | 254065 |
rs188811447 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763368 | AAAATCATCATATAC[A/C]CCAATAGCTAACTAT | 254065 |
rs188835928 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80679776 | CTGAAGAGTACTGAT[A/G]AATGTGAGAACAGCT | 254065 |
rs188873117 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80725631 | GCTTTATGTTATATG[C/T]CTATATAACATATAA | 254065 |
rs188902036 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80782167 | AACAGAAACATAGGC[C/T]AATGGAACAGATTAG | 254065 |
rs188905150 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800823 | GTTAAAACTTCCTAT[C/T]ACTCACCTTTGAAAA | 254065 |
rs188982459 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715362 | AATTTCTGTTTATCA[A/G]TTATGGAAAAAAATG | 254065 |
rs188991000 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80752119 | CTGGGCTCAACTGAT[A/C]CTCCCACCTCAGCCT | 254065 |
rs188995095 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736582 | TCCAGTTCCATTCAA[C/T]TGAAGTATATAATTT | 254065 |
rs189010290 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768249 | ACAAAGATACTCCTT[A/G]AGAAAATCAACCCCA | 254065 |
rs189045413 | snp | C/T | 0.000297299 | 0.0121886 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717721 | TTCGAAGCCTGATGT[C/T]TGGGGAAGAAGATAT | 254065 |
rs189047883 | snp | G/T | 0.0199298 | 0.0978146 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672415 | AAGGAAGAGAGGGAG[G/T]GAGGGAGGGGGGAGG | 254065 |
rs189102662 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756765 | TCACACACTTCCTTG[A/G]GGGGAGGAGAATGCT | 254065 |
rs189128835 | snp | A/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80794530 | AAATAAATAAAAAAA[A/T]ATATATATATCTCTA | 254065 |
rs189138658 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80703822 | AATAACTTGACACTA[C/T]AGACTACCTGAAAAC | 254065 |
rs189148909 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743255 | TGAAGTCCACTTGAT[C/T]ATGGTGGATAAGCTT | 254065 |
rs189153159 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766968 | GATTATAGCCCGCAC[A/C]TGTCTCTGCGAATCC | 254065 |
rs189195485 | snp | C/G | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674552 | CAATTTAGTCTAAAT[C/G]CCCAAGAGATAAATA | 254065 |
rs189312840 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80689276 | ATACGAGGGTCTGCT[A/G]AGTACTACTTCCATT | 254065 |
rs189320837 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80733106 | CCGCACTCCAGCCTC[A/G]GCAACAGAGCAAGAC | 254065 |
rs189328259 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670906 | AAAATACACAGTATA[C/T]ATATATCAAAGATAC | 254065 |
rs189331034 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712034 | CTTTCATCAACAGCA[G/T]TCTTAAGATTCTTAA | 254065 |
rs189333552 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80748054 | CAACATGTTAGTCAC[A/G]CTGGTCTTGAACTCC | 254065 |
rs189336158 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772103 | TACCATTTAACCCAG[C/T]AATCCCATTACTGGG | 254065 |
rs189338304 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793034 | GGGCGAGGTGGCACG[C/T]GCCTGTAGTCCCAGC | 254065 |
rs189349556 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715875 | AGTGATCTGGTAATA[C/T]AGTTAAGGTTCTACT | 254065 |
rs189353661 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766690 | TGCAGCTCCCAGCGT[A/G]ATCGATGCAGAAGAT | 254065 |
rs189356291 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743821 | TATTTATAGAACTTT[A/T]TAAATCATCTTTTTA | 254065 |
rs189371388 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777154 | TAAGACCCCCCCCCA[A/C/G]GAAAAACCTCCTGAG | 254065 |
rs189389719 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740881 | TATTAATACAAGGTA[A/T]GCCAATATTCAAGTT | 254065 |
rs189393753 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80772445 | GACACAGGGCGGGGA[A/C]CATCACACCCTGGGG | 254065 |
rs189394013 | snp | G/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80692754 | GTCAAAGAAAACAAA[G/T]AACTTTGCTTTGACT | 254065 |
rs189398085 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80736150 | GCCTAACATCAAACA[C/T]GGAGTATTTTCAAAT | 254065 |
rs189455573 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799521 | TGTAACATTTTGCCT[A/G]GGTCTGATTGGTTGA | 254065 |
rs189554142 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80693841 | GCAGAGCATTAAAGT[C/T]CAGAACTTTTGCAGC | 254065 |
rs189562315 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670489 | GGCATGATCACAGCT[C/T]ACTGCAGCCTTGACC | 254065 |
rs189636782 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80760910 | TTAGTACCAGAGTGT[A/G]GTAATTCCTACCTAT | 254065 |
rs189642480 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80694485 | CCGACAACGTGCGCC[A/G]TGTGCCTGGAAAAGC | 254065 |
rs189652308 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80736761 | CAAGGCCTTTATCAT[A/G]TGGGCTTCTCAGGCT | 254065 |
rs189687387 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714820 | ATTTCTACTATTTGC[A/G]GACAATATAGAAGAA | 254065 |
rs189694150 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80681555 | GTTTTCAGGAAAGTT[A/C]AACAGGCTACTTTTT | 254065 |
rs189698017 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751351 | TCAAAACATGACATT[G/T]TACGCCTTGAATATA | 254065 |
rs189767665 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770698 | AACTGGGACAAGACA[G/T]GGATGCCCTCTCTCA | 254065 |
rs189771975 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80790758 | CAAAATAATGTTGAC[A/G]GTATAGCTAAAAATA | 254065 |
rs189774123 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679169 | AGTCTGTGGTATCTT[C/G]TTATGGAAACCCAAG | 254065 |
rs189788386 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702147 | AATGTTGCCATTAAG[A/C]AATCAATTATATAAA | 254065 |
rs189788721 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748549 | GGAAGACTTTTTATT[A/G]CCGACTCAATCTCAT | 254065 |
rs189799459 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766857 | ATTTCCCTTTCCTAG[C/T]CAACGGAAGCCTTGA | 254065 |
rs189801434 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80724502 | CTTGTATGAGACATA[C/T]CTTAAAGAACATCCG | 254065 |
rs189809801 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80785163 | CCTCAAACAATACCA[C/T]AAATATTAATTACAT | 254065 |
rs189816427 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742263 | CTGTTCTGTTCCATT[A/G]GTCTATATTTCTGTT | 254065 |
rs189826587 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80807179 | CAACAGAAAGACTGA[C/T]TACAAATTAACCTGG | 254065 |
rs189852511 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80727139 | CATATTTGTATTTAG[C/T]AAGCACACTTTTATT | 254065 |
rs189858495 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80706461 | CTATTTTTAAGGTTT[A/G]AAATTTTTTTTTATT | 254065 |
rs189868907 | snp | C/T | 2.85026e-05 | 0.00377498 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745679 | CAGATGAAGGGAAAA[C/T]ATGACCAAAGCGACT | 254065 |
rs189927857 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762207 | AACATGTTTTGCCTT[C/T]CTCTCTTTGAACTAG | 254065 |
rs189929587 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788475 | GAAAAGATACCAACC[A/G]ACAGTATCAGAAGAT | 254065 |
rs189939457 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709634 | TCAGTAAACACACAA[A/G]GAACATATATAAAGC | 254065 |
rs189945767 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671557 | CAATTGATTCCAAAC[A/T]ACTTGGAATTTTATT | 254065 |
rs189966316 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80695691 | ATTCCTGTTTGTATA[A/C]TAATAGAGTAGGTAT | 254065 |
rs189999172 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783262 | CATAGTAGTGCACAC[A/C]TGTAGTCCCAGCTAC | 254065 |
rs190025193 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684616 | TAGTTAAGGGTCAGG[G/T]TCAAATTGGTCATGT | 254065 |
rs190139070 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745891 | ATGATTTTATGAACT[C/G]CAGTTTACTACAAGA | 254065 |
rs190143470 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80728682 | AAAGGAACCTGGAAC[C/T]TAAATTTCCTGTGTC | 254065 |
rs190150621 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80711083 | TATTCAGAATTATTA[C/T]AGGATGAAGCAAGAC | 254065 |
rs190181312 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80747765 | AGAAACAATGTAGAT[C/T]GTCAAGTTCATTTTG | 254065 |
rs190187492 | snp | A/G | 0.00158814 | 0.0281345 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811720 | CATTTAATCTTTACA[A/G]TGACCCTAGGAGATA | 254065 |
rs190187628 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745397 | TAAACATTTTTGTTC[A/G]TTCGTTTACTTATAT | 254065 |
rs190192001 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80779142 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 254065 |
rs190220038 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699506 | AATATGGAGCCACAT[A/G]GGTATTATATATGTA | 254065 |
rs190226049 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80739740 | CTACACACCTATAAG[A/C]TTAATTTATAAATTA | 254065 |
rs190253011 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805060 | GATCAGGATACGTCA[A/G]TACTTAACTGCAAGC | 254065 |
rs190285476 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80806282 | AATATTTAAAAGATA[C/T]GTTAAAATTGAGTAT | 254065 |
rs190356620 | snp | A/G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80762570 | GGGTATGTGTTGGGG[A/G/T]GGTGGGGAAAGGAGA | 254065 |
rs190361021 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80781289 | ATCATTGTCCCTCCC[C/T]GTGTGCTCTCAGGCG | 254065 |
rs190365549 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80802386 | GGCGGAGGTTGCAGT[A/G]AGCCAAGATCGCACC | 254065 |
rs190411349 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688361 | CTTTAAACAAGAATC[A/G]GAAAGGAGGGGAACA | 254065 |
rs190414539 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80732763 | TAGCTCTAAGTCATG[G/T]GGTAAAAAGCTGTGA | 254065 |
rs190426344 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80696360 | AGCAACCACCATGTT[C/T]CAAACATTCAATTAG | 254065 |
rs190427172 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766133 | CCCAATGAATCCGGT[A/G]GGCTTTATTCAATAC | 254065 |
rs190439155 | snp | A/G | 0.00528398 | 0.051128 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672337 | ATATAGGCCGGGCAC[A/G]GTGGCTCATGCCTGT | 254065 |
rs190441274 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80717370 | GTTTTGCATTTTCAA[A/T]ATTCCCCAAAGCATT | 254065 |
rs190441658 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674987 | TATATACTAAGAAGT[C/T]TGTTTTATCCCATGA | 254065 |
rs190455303 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80754079 | GTATTTTCATGGAGA[C/T]TACACTGAATCTGTA | 254065 |
rs190455666 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738259 | GTTTAATAAAAAATC[A/G]TGTTATGGATTGTTT | 254065 |
rs190460199 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721144 | TATATACACTGAAAC[G/T]TAATGATTATTTCTG | 254065 |
rs190473048 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80770036 | GACACATACACCCTC[A/C]CAAGACTAAACCAGG | 254065 |
rs190478754 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789928 | TCACACCCATAATCC[C/T]AGCACTCTGGGAGAC | 254065 |
rs190495495 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80756361 | ACAAAAATTAGCTGG[A/G]CCTGGTGGTGCATGC | 254065 |
rs190510049 | snp | C/T | 0.000281703 | 0.0118648 | intron-variant | BRWD3 | GRCh38.p7 | X:80691027 | AAGCTATAAATTTTA[C/T]AATAAGTGATTAAAA | 254065 |
rs190510125 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740976 | CAGGTTTGTTACATA[C/T]GTATACATGTGCCAT | 254065 |
rs190517366 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783940 | GGATAGTGGGAAAGA[A/G]CGGGGAAGTGGGGAT | 254065 |
rs190520621 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773512 | TTATATTAGTTACAT[A/C]TTTCTGATTTAAGAT | 254065 |
rs190522257 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80757927 | TCAAATAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 254065 |
rs190690407 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80723051 | GAAGAACTAAAGCAA[C/T]AACCCAGTAGATATA | 254065 |
rs190694859 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700369 | TATTTTAAAGTATAT[A/G]TGCCCCTCCATATCC | 254065 |
rs190696262 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80690651 | CAAAACAAAAAAATT[A/G]CTTGGCTCCTTTCCT | 254065 |
rs190751603 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80759883 | TAGTATAATCCCATA[C/T]AGATTTCTCACTCCT | 254065 |
rs190770431 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797094 | AGTTTATAATTCATA[A/C]CCTGCACATTCAGGC | 254065 |
rs190796900 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719203 | AAAGGGCTAGACTTA[C/T]CGTAGCACTTCACTT | 254065 |
rs190814270 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80780730 | GAGTACAAAGAGGAG[A/G]AAGGTGGTAAGTAGA | 254065 |
rs190828314 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754481 | ACTTCCTCTTTTCCA[A/G]TTTGGATGCCTTTTA | 254065 |
rs190963259 | snp | A/T | 0.100346 | 0.200259 | intron-variant | BRWD3 | GRCh38.p7 | X:80713416 | GTGCTCTCTGAAACA[A/T]GTGCTGTGTCCACTC | 254065 |
rs190996181 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795824 | TAGTCCCAGCTACTC[A/G]GGAGACTGCAGTGGG | 254065 |
rs191014218 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80785961 | CTTGAACCCAGAAGC[C/G]GGGGTTGCAGTGAGC | 254065 |
rs191016328 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80775060 | GCTGGCAAACTAAGG[A/C]CCATGGACCAAATGT | 254065 |
rs191048583 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737173 | CCTATATAGTCCTCC[A/G]TTGGTATCATTGAGA | 254065 |
rs191061333 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762375 | ACAGAGAAGGGGCAC[A/G]AACTTGGGTCAAATG | 254065 |
rs191063832 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80707366 | CCAATTTCCTACGAG[A/T]ACATAATTTCGTATT | 254065 |
rs191071139 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80769579 | ACCAGAATCTCTGGG[A/G]CACATTTAAAGCAGT | 254065 |
rs191076426 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80801512 | TGAGCAACCGCGCCC[A/G]GACGAGAAAACATTT | 254065 |
rs191097024 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80786954 | CAGGGTTATCTATAT[A/G]AAGAATCCCAAAGAA | 254065 |
rs191104865 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810226 | GTTTTGACTCGACTC[A/C]TTTCCCCTTTTTCCT | 254065 |
rs191105042 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80761073 | TGGTTAGCTTAGTAT[C/T]AGACCCTCAATATTA | 254065 |
rs191283783 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80685618 | AATTATGACTTAAGT[C/T]TCAAAGATCCATACA | 254065 |
rs191300594 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716833 | TGCTTTCTATGTTTT[A/G]AGTAAATAATCATTT | 254065 |
rs191300815 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753598 | TCATAAATTTTTTGC[A/C]TAGACCAATGTCCAA | 254065 |
rs191312245 | snp | A/T | 0.01368 | 0.0815649 | intron-variant | BRWD3 | GRCh38.p7 | X:80686607 | TGTATTAAATAAACG[A/T]CTGAAATAAAAGTCG | 254065 |
rs191318575 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | BRWD3 | GRCh38.p7 | X:80731095 | ATACATACTGCCAAA[C/T]TGTTTCCCTGAAAAG | 254065 |
rs191319836 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789437 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGTTCACT | 254065 |
rs191326872 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709206 | CTCTTGCTGGCATAT[C/T]TGATACCCTCACCAA | 254065 |
rs191332793 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746416 | TTGTTCGCTTTGCCT[C/T]GTTCTGCATTTTCTT | 254065 |
rs191349375 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782250 | TCCCAAGAACACATA[C/T]TGGAAAAAGGACAAT | 254065 |
rs191351480 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80763973 | TTAAGGCTTACTACA[C/T]AGCTACAGAAATCAA | 254065 |
rs191504447 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80682355 | AGTTTAGGAAACAAA[C/T]AAAAAAAGACCTCTT | 254065 |
rs191512170 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80726331 | ATAACATATAACATG[A/T]TTACATGTTATGTCT | 254065 |
rs191580426 | snp | A/G | 0.0338441 | 0.125605 | intron-variant | BRWD3 | GRCh38.p7 | X:80713639 | CTCCACTATTGTCCT[A/G]TGACCCTGCCAAATC | 254065 |
rs191618772 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80749881 | ACAGCATGATACTGA[C/T]GTAGAAACAGACACA | 254065 |
rs191628513 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785541 | TTTGATTAACTATAC[C/G]AACGACGGAAACATT | 254065 |
rs191685872 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80698311 | TTATATATTAGCATA[C/T]AGCAAAGCTAGAATT | 254065 |
rs191690327 | snp | C/T | 0.0157677 | 0.0873799 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674286 | TCTAGAAAATCTTGA[C/T]ATTTGGGAAATAAAT | 254065 |
rs191755490 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705725 | AATTTTAACACAATG[C/T]TAAGTATATATCTAC | 254065 |
rs191816278 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746954 | ACAATTAGAACACAT[A/G]AGAGACCTGAGTAGT | 254065 |
rs191828590 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764149 | TGGTGCTGAAGCAAT[C/T]TGACATACAGAAGTG | 254065 |
rs191841070 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783087 | ATCATCAGAGAAATG[C/T]AAATCAAAACTATGA | 254065 |
rs191853006 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80804613 | TTTAAAAAGTTTCCA[A/T]ATCACCATTTCAATA | 254065 |
rs191853394 | snp | C/G | 0.0570788 | 0.159001 | intron-variant | BRWD3 | GRCh38.p7 | X:80701542 | CAACAGAGCGAGACT[C/G]GTCAAAAAAAAAAAA | 254065 |
rs191863707 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742211 | GGTTTGCCAAAGATC[A/G]GATGGTTGTAGATAT | 254065 |
rs191866440 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80719923 | TAACGACATTTCAGT[C/G]AAAGATAAACCACAT | 254065 |
rs191887272 | snp | C/T | 2.28258e-05 | 0.00337822 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734124 | TTCTCTTACCGTATG[C/T]GACTCTAATTCAGCA | 254065 |
rs191921508 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766876 | CGGAAGCCTTGAGAG[A/G]CAGCACCTGGAAAAC | 254065 |
rs191960004 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755460 | TTTACACCTAATAAA[C/T]TAGCATTTCTAAAAA | 254065 |
rs191962119 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80771859 | GCAGCCAAGAGACAC[A/G]TGAAAAAATGCTCAT | 254065 |
rs191979716 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792379 | ACTTGGGTACATGTT[C/T]GTATTATGAAATACT | 254065 |
rs192047183 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80773972 | GAAAATGCTTTACAT[A/G]TATTTGGTGTTCACG | 254065 |
rs192068986 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80809082 | TGAGGAGCAGCTCGG[C/G]CCATCAACCCATTCC | 254065 |
rs192137224 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720799 | GGTAAGTGCTTTATA[A/C]AGTCATACCATTCTT | 254065 |
rs192143432 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80699023 | CTTCGAGACTAGCCT[C/G]GTCAATGTGGCAAAA | 254065 |
rs192154518 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739116 | ATAATCTAGACCACA[A/G]GTGATAGTGCCTTAA | 254065 |
rs192156847 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80677992 | AGCAAGCCAGTATAA[A/C]CAGAGTGGAATAGAA | 254065 |
rs192172884 | snp | C/T | 2.37643e-05 | 0.00344696 | intron-variant | BRWD3 | GRCh38.p7 | X:80723715 | TGACACAATCCTAAA[C/T]TATACTCTACAGCAA | 254065 |
rs192174831 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80759134 | ACGAATGAAGGTTAA[C/G]ATTGCAAAGACTACA | 254065 |
rs192180827 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724857 | TCCTCTGCACTAGGT[A/T]TACTTTAATTAACCA | 254065 |
rs192196329 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80743144 | CCTTTTCTGCATCTA[C/T]TGAGATAATCATATG | 254065 |
rs192201129 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80693332 | TAATTAGCATCATCA[G/T]TAGGCACACTTCTTA | 254065 |
rs192201825 | snp | A/T | 0.00475684 | 0.0485365 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669969 | TCAAATTAAATATCA[A/T]TTTGTTAATTAATAA | 254065 |
rs192213215 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80775697 | GTCTAATACTTAAGT[C/T]TGGATATTAGAGTCC | 254065 |
rs192217788 | snp | A/C | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80760070 | CTGCATCAAGTTTCT[A/C]TAACTCTTCATGTTA | 254065 |
rs192218135 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714831 | TTGCGGACAATATAG[A/C]AGAAGAGAAATTGAG | 254065 |
rs192233958 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798302 | GGTCTTATAAGGGTA[A/G]TTAACTGCTTACTTG | 254065 |
rs192291441 | snp | A/G/T | 2.39223e-05 | 0.00345841 | intron-variant | BRWD3 | GRCh38.p7 | X:80692171 | AAAAAATAAGAAGAT[A/G/T]CAAATCAAATTAATC | 254065 |
rs192301105 | snp | A/G | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80735673 | GCCAGGCATAGTGGC[A/G]GGTGCCTGTAGTCCC | 254065 |
rs192339199 | snp | C/T | 0.0068637 | 0.0581785 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672745 | ATGGACTTTACATGT[C/T]GAAAGTTCCATCCCT | 254065 |
rs192359129 | snp | A/T | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80668988 | GTAGCAACAGTCTAG[A/T]CTTTTTTTTTTTTTA | 254065 |
rs192375866 | snp | A/G | 0.000533426 | 0.0163226 | intron-variant | BRWD3 | GRCh38.p7 | X:80691812 | CTAAAATTTTTTCAC[A/G]TTCATCATACCCAGG | 254065 |
rs192390730 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80713808 | TTTTGGAACTGAAAT[C/G]TAAACTCTGCTCTTT | 254065 |
rs192539138 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80777250 | ATTCTGTTTATTATC[A/T]CAGGAAATATTCTGA | 254065 |
rs192610371 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80750294 | AATGATTAGCAGACA[A/G]ATGATACAACTCACA | 254065 |
rs192614945 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734501 | TTTAGAAATGCAATG[C/T]TCCAAAATTATTTAT | 254065 |
rs192628464 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80767210 | GTGGTTCTCCCAGCA[C/T]GGCGTTTGAGCACAA | 254065 |
rs192693959 | snp | A/T | 0.00370173 | 0.0428621 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669397 | GATATCATGGGCATA[A/T]TTTTTGCTCTATAGG | 254065 |
rs192694219 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714126 | GCATCTTTTTAAGTC[C/T]GATAACAAACATTTA | 254065 |
rs192722275 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697389 | ATATATTGCATAATG[G/T]TGGGGTTTGAGTTTC | 254065 |
rs192759137 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804118 | TTGCATATAAAATGA[A/G]GGTAATACAATCTAT | 254065 |
rs192763674 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80709694 | AGATGAGAATAAATT[C/G]CCCAAAATAAAGTCA | 254065 |
rs192765020 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80738914 | GGCTGAGAATACAGA[A/G]CACTGTGAGTCACTG | 254065 |
rs192767734 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80771281 | GAACCAAAAAAGAGC[C/T]CGCAATGCCAAGACA | 254065 |
rs192804679 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80802593 | ATTTTAAAATGTAGC[C/G]AACAATTCATTTGCA | 254065 |
rs192883995 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686064 | AGTATTCCATGGTGT[A/G]TATGTGCCACATTTT | 254065 |
rs192889133 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729800 | CAGATGCAAACTTCA[C/T]GTCTACAATTAACTT | 254065 |
rs192892753 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80763410 | TACAACAGATTTCAT[C/T]CCATATCTTAAATTC | 254065 |
rs192906428 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80679664 | ATATAAGCTAATCAA[G/T]AGAGTATAGAAGCTT | 254065 |
rs192934857 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751554 | TAAGCAAAATACATT[G/T]TTTTAAAACTATTTT | 254065 |
rs192943336 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787516 | GTGCCACGATAATCC[A/G]ATGGGGAAAAGGATG | 254065 |
rs192963163 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687390 | TTGAATGATTTTTTT[G/T]CCCAGAAATCCTTTG | 254065 |
rs192969259 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80754939 | CTTGAACCCAGAAGG[C/T]GGAGGTTGCAGTAAG | 254065 |
rs192977574 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732022 | AATTCCACACCTGGC[C/T]TCTTGTGATGGGTCA | 254065 |
rs192982376 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80791222 | CTATATATAAAATAA[C/T]GTAATTTTTTAGAAG | 254065 |
rs193085574 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | BRWD3 | GRCh38.p7 | X:80708554 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 254065 |
rs193085939 | snp | A/C/T | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674617 | AGTTTCAAATAGGAA[A/C/T]GTTTTGAATCTCTAC | 254065 |
rs193126378 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80703870 | TCCCTTGACTACCAC[A/G]TGAATTCAAATGCAA | 254065 |
rs193129429 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80743382 | TATGTCTCTGACAGG[C/T]TTTGATATCAGGATG | 254065 |
rs193132693 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746029 | TCAAAGAGACTGTCA[C/T]TTTAAATATATAGGT | 254065 |
rs193135448 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776834 | GTAGTTAATTCCCAC[A/T]TGTTCCAATTTGCCT | 254065 |
rs193154592 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781534 | CCAAGTGCTGTTGGG[A/G]AGGTTGGCCGATGAC | 254065 |
rs193163675 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702849 | AAATTAAAAACTGTG[C/T]AAAAACATTTAATTG | 254065 |
rs193168496 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736267 | TACCTTATAAAAAAT[C/T]TAAAATATCAAAAAA | 254065 |
rs193175546 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768172 | CAGGATATTTTCCAG[A/G]AGAACTTCCCCAACC | 254065 |
rs193179222 | snp | C/G | 0.00158814 | 0.0281345 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810536 | AGTTTAACACGTGCC[C/G]TATCTACGGCTGGGA | 254065 |
rs193225475 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80679956 | TCAGAGGAGACACTA[A/C]AGATGTAAACTGGGA | 254065 |
rs193282855 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80725785 | TGTTACATGCCTATA[A/T]AACGTATAACATGTT | 254065 |
rs193285124 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80760557 | TGTATGATAGTCTAA[G/T]GTGCACTGGAATATT | 254065 |
rs193291325 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799032 | AATTATAATGATAGC[A/G]ATCATTAACACAAAG | 254065 |
rs199500831 | in-del | -/AT | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80725993 | ATATGTCTATATAAC[-/AT]ATAACATGTTTACAT | 254065 |
rs199514397 | in-del | -/A | 0.376123 | 0.215854 | intron-variant | BRWD3 | GRCh38.p7 | X:80733145 | GCAAGACACCGTCTC[-/A]AAAAAAAAAAAAAAA | 254065 |
rs199568218 | snp | C/T | 4.57739e-05 | 0.00478381 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716168 | TTACCCTTTGAGTAG[C/T]GTAAGATGGCTTTTT | 254065 |
rs199589092 | in-del | -/A | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80679581 | GTGGAAGACAAAAAC[-/A]AGCAAAAAACAGTGG | 254065 |
rs199612307 | snp | A/C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80735841 | CCTAAAATCTCTTAA[A/C/T]AACCTATTGAAGTAG | 254065 |
rs199636817 | in-del | -/TCT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680706 | GATGACTTTGGAAAC[-/TCT]CCTTTCTTATTAATA | 254065 |
rs199647124 | in-del | -/T | 0.0121112 | 0.0768695 | intron-variant | BRWD3 | GRCh38.p7 | X:80748686 | TTTTAACAAACCAAC[-/T]TTAAGATTTGTTAAT | 254065 |
rs199649388 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727423 | ATCTGGGGAGAATCT[A/G]TTTCTGCTCTCTGTG | 254065 |
rs199676970 | snp | A/T | 6.96144e-05 | 0.00589935 | missense | BRWD3 | GRCh38.p7 | X:80676721 | GTGGACACAAAATTG[A/T]CATTATCAGAATCAT | 254065 |
rs199694181 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680022 | TATGTTTCAACATTT[C/T]TTACATAGCCACTAT | 254065 |
rs199709224 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779622 | TTTTGGTGAAGCTTC[G/T]TTGGGGGTTTCCTAA | 254065 |
rs199737675 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726344 | TGTTTACATGTTATG[C/T]CTGTATAACATATAA | 254065 |
rs199743217 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756501 | GAGCGAAACTCTGTC[A/T]CAAAAAAAAAAAAAA | 254065 |
rs199783122 | in-del | -/TTCT | 0.0714214 | 0.174956 | intron-variant | BRWD3 | GRCh38.p7 | X:80740911 | TAGAACCTGTTTATA[-/TTCT]TTTTTTAAATTATAC | 254065 |
rs199808156 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800761 | AAAAAAGAAAAAAAA[-/A]GACAGCAGGCAGGCC | 254065 |
rs199833376 | in-del | -/AT | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80726150 | ATATGTCTGTATAAC[-/AT]ATAACACGTTTACAT | 254065 |
rs199874346 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793124 | CCGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGT | 254065 |
rs199879142 | in-del | -/ATTATT | 0.481659 | 0.0939889 | intron-variant | BRWD3 | GRCh38.p7 | X:80751982 | ATTTATTCATATTTC[-/ATTATT]ATTATTATTATTATT | 254065 |
rs199899212 | snp | A/G | 0.000208686 | 0.0102127 | intron-variant | BRWD3 | GRCh38.p7 | X:80681961 | TATCAGAATTAAACC[A/G]AGATGCAGAACACCA | 254065 |
rs199899379 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742403 | ATGTGGGCTCTTTTT[C/T]GGTTCTGTAGTTTTT | 254065 |
rs199948186 | snp | A/T | 2.30171e-05 | 0.00339235 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80724978 | CCGGTCAAGGTCCCA[A/T]ATAAAAATGTTCCCA | 254065 |
rs199953219 | in-del | -/AG | 0.299416 | 0.245067 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809737 | AGAGAGAGAGAGAGA[-/AG]AGAGAGAGAGAGAGA | 254065 |
rs200009453 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742408 | GGCTCTTTTTTGGTT[A/C]TGTAGTTTTTTCCAA | 254065 |
rs200025344 | snp | A/G | 2.33762e-05 | 0.00341871 | intron-variant | BRWD3 | GRCh38.p7 | X:80691032 | ATAAATTTTATAATA[A/G]GTGATTAAAAAAAAA | 254065 |
rs200051261 | snp | A/G | 0.000215999 | 0.01039 | intron-variant | BRWD3 | GRCh38.p7 | X:80744288 | ATAGGTTTATAATGA[A/G]GCAGAAATTCACAAT | 254065 |
rs200060316 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790213 | AAAAAAAAAAAAAAA[A/T]AAAAAGATATACCTT | 254065 |
rs200066121 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801457 | TCCTGACCTCATGAT[C/T]CACCCACCTAGGCCT | 254065 |
rs200074534 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730388 | TGAAATATTATTTAG[A/C]AAAAGAAAGAAAGAA | 254065 |
rs200083602 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790929 | TAGCAATACCATGTT[-/C]AATGAGACTCAACTT | 254065 |
rs200102928 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801409 | TTTTAGTAGAGACAG[G/T]GTTTCACCATCTTGG | 254065 |
rs200104439 | snp | C/G/T | 0.189048 | 0.242456 | intron-variant | BRWD3 | GRCh38.p7 | X:80727724 | TCAAGGAGTTGACAA[C/G/T]TTGAGATTGGGTAAT | 254065 |
rs200157039 | in-del | -/A | 0.32699 | 0.23785 | intron-variant | BRWD3 | GRCh38.p7 | X:80798626 | GTGTATAATACGGGG[-/A]AAAAAAAAAAAGAGT | 254065 |
rs200166730 | snp | A/G | 9.16328e-05 | 0.00676816 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719521 | GCTCTATTAACTGGT[A/G]AATGTGGAACATCTC | 254065 |
rs200199122 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777693 | ACGAGCCACCATGGC[C/T]GGCCTCTGATTTTTT | 254065 |
rs200199261 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756363 | AAAAATTAGCTGGGC[C/G]TGGTGGTGCATGCCT | 254065 |
rs200214471 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781163 | TAAAAAACAAAATTC[-/T]TTTTTTTTTGAAGTT | 254065 |
rs200357216 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726058 | TGTTATGTCTATATA[-/AC]ACAACATGTTTACAT | 254065 |
rs200361750 | in-del | -/AATTGTACATTCGTCATTCTA | 0.0204488 | 0.0990265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685672 | ACTTTAAGGTGAAGG[-/AATTGTACATTCGTCATTCTA]AATTGTACATTCGTC | 254065 |
rs200390072 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756526 | AAAAAAAAAAAAAAA[C/T]AAACAATGTCAACAC | 254065 |
rs200402115 | in-del | -/C/CC | 0.487487 | 0.0788782 | intron-variant | BRWD3 | GRCh38.p7 | X:80809411 | CCCATTCCCTTAGCA[-/C/CC]CCCCCCCACCCCCCG | 254065 |
rs200412890 | snp | A/T | 0.48 | 0.0979796 | intron-variant | BRWD3 | GRCh38.p7 | X:80726076 | CAACATGTTTACATG[A/T]TGTCTGTATAACAAC | 254065 |
rs200424135 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80704868 | ATAAATCAAAATTAT[A/G]GATACCTAAGTATAG | 254065 |
rs200446613 | snp | A/G | 0.000578409 | 0.0169962 | intron-variant | BRWD3 | GRCh38.p7 | X:80716141 | GTATCCCAAAGTATT[A/G]TAAAACTATACTTAC | 254065 |
rs200450954 | in-del | -/A | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80734942 | AAATTATGAATAAGG[-/A]AAAAAAAAATCAACC | 254065 |
rs200456572 | snp | G/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686940 | GGCTCAATAGTTCCT[G/T]GCATTGTTTTTTCCA | 254065 |
rs200460265 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680026 | TTTCAACATTTCTTA[C/T]ATAGCCACTATAAAA | 254065 |
rs200470479 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756502 | AGCGAAACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 254065 |
rs200487205 | in-del | -/A | 0.0522189 | 0.152914 | intron-variant | BRWD3 | GRCh38.p7 | X:80727722 | AATCAAGGAGTTGAC[-/A]AGTTGAGATTGGGTA | 254065 |
rs200518888 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795353 | ATTGTGTATATATAT[-/AC]ACACACACACACATG | 254065 |
rs200563834 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721496 | AGCCTTAATTCCCTA[A/G]CAATGATATGAAATT | 254065 |
rs200610851 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767362 | CTAGAAGAAGTATCA[G/T]GCAGCAATATTTTGC | 254065 |
rs200633293 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798388 | AAGAACTCTTACCCC[A/G]AATAGTTTTTTTTTT | 254065 |
rs200684993 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80683495 | AGTAGGCAAATATAT[A/G]TTTACTGTGCAACTG | 254065 |
rs200686196 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742404 | TGTGGGCTCTTTTTT[G/T]GTTCTGTAGTTTTTT | 254065 |
rs200693743 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80768789 | ACACAGACTGGCAAA[C/T]TGTATAAAGAGTCAA | 254065 |
rs200701062 | in-del | -/ATT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680197 | CAAACTTCAAATAGC[-/ATT]TGAACATGTTAGAAC | 254065 |
rs200711043 | in-del | -/CTC | 0.0240739 | 0.107039 | intron-variant | BRWD3 | GRCh38.p7 | X:80680707 | ATGACTTTGGAAACT[-/CTC]CTTTCTTATTAATAT | 254065 |
rs200718968 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698601 | GTAATCCCAGTTACT[C/T]GAGAGGCTGAGGCAG | 254065 |
rs200751676 | snp | C/T | 0.000509194 | 0.015948 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676917 | CCCTAGTGCCACCTC[C/T]ACCTCTTCCTCGACT | 254065 |
rs200785065 | snp | A/C/T | 0.000114658 | 0.00757088 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681471 | ATCATCAAGTAGATA[A/C/T]AGTGAAAGCCCTTCA | 254065 |
rs200788890 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742401 | CAATGTGGGCTCTTT[A/T]TTGGTTCTGTAGTTT | 254065 |
rs200802103 | snp | A/G | 2.27998e-05 | 0.0033763 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722721 | GGGTTTGTTCATCCA[A/G]TACATAGTTATTGGC | 254065 |
rs200825507 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80802974 | GCCGGGCGTAGCGGG[C/T]GCCTGTAGTCCCAGC | 254065 |
rs200926213 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801414 | GTAGAGACAGGGTTT[C/T]ACCATCTTGGCCAGG | 254065 |
rs200939386 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80719071 | GTGTATTTTTTTTTT[A/T]TATTCAAGAGAAGAG | 254065 |
rs200943021 | snp | C/G | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692150 | CTCATTATTGTCCCA[C/G]CTATTAAAAAATAAG | 254065 |
rs200981902 | in-del | -/T | 0.496294 | 0.0428865 | intron-variant | BRWD3 | GRCh38.p7 | X:80753273 | GCCTGTGCTTTTCAG[-/T]TTTTTTTTTTTTTTT | 254065 |
rs201004001 | in-del | -/A | 0.017851 | 0.0927731 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670583 | CATGCCCAGCTAATT[-/A]AAAAAAAAAATTGTT | 254065 |
rs201017662 | in-del | -/A | 0.0168099 | 0.0901243 | intron-variant | BRWD3 | GRCh38.p7 | X:80772619 | CTTAAAGTATAATTT[-/A]AAAAAAAATAAATGA | 254065 |
rs201024289 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80696893 | ACCAATAAATTATTA[C/T]TTTCAATATAATTAC | 254065 |
rs201065206 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688994 | TTTTCATGAAAAAAA[A/T]AAAAAAAAACAGCAT | 254065 |
rs201065966 | in-del | -/AAAAAAAAAAAAAA | 0.490403 | 0.0686035 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793161 | GCAAGACTCTGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAATT | 254065 |
rs201088235 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803485 | AGAGCCCATCTGTGG[-/A]AAAAAAAAATGCCAA | 254065 |
rs201106928 | in-del | -/AGAAGTTAA | 0.167375 | 0.235951 | intron-variant | BRWD3 | GRCh38.p7 | X:80679733 | ATGATATAGAGATTG[-/AGAAGTTAA]AAACTAAAAAAAGAC | 254065 |
rs201155478 | in-del | -/GTCAGA | | | cds-indel, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677157 | AGAGTCAGAGTCAGA[-/GTCAGA]ACCACAGGTACTTTC | 254065 |
rs201174107 | in-del | -/CACT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727720 | TAATCAAGGAGTTGA[-/CACT]CAAGTTGAGATTGGG | 254065 |
rs201206298 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790327 | AAAACTGCCTCAAAT[C/T]ACAAACTGGAAAGAT | 254065 |
rs201215263 | in-del | -/T | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80741421 | TCCTTTGGGTATATA[-/T]CCCAGTAATGGGATG | 254065 |
rs201232963 | in-del | -/T | 0.0302564 | 0.119217 | intron-variant | BRWD3 | GRCh38.p7 | X:80713696 | ATCAATAAAAAAATA[-/T]AAAAATAAAAAAAAC | 254065 |
rs201254657 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795692 | TTGAGACCAGCCTGG[-/G]CAACATAGCGAGATC | 254065 |
rs201259293 | snp | A/G | 0.0101738 | 0.070593 | intron-variant | BRWD3 | GRCh38.p7 | X:80730389 | GAAATATTATTTAGC[A/G]AAAGAAAGAAAGAAA | 254065 |
rs201263688 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755288 | ATATAAAACTAATGA[G/T]CTATAAGAACACCAT | 254065 |
rs201299393 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80680027 | TTCAACATTTCTTAC[A/T]TAGCCACTATAAAAT | 254065 |
rs201312766 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679012 | CTCTGTAGAGGCAAG[A/G]CCACGTGAGGACAAA | 254065 |
rs201325619 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726009 | ATAACATGTTTACAT[A/G]TTATATGTCTATATA | 254065 |
rs201335896 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805094 | TTTAATAAAAAAGCA[A/C]CTTCCCTTGTGTTCA | 254065 |
rs201336724 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742409 | GCTCTTTTTTGGTTC[A/T]GTAGTTTTTTCCAAT | 254065 |
rs201368296 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80677596 | GCCATGAGGTTTAGG[C/T]AGAAGTTTTAAGGGC | 254065 |
rs201368637 | snp | A/C | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80690046 | CATTGAAAGTCCTGG[A/C]ATTATGTTCAATATA | 254065 |
rs201368659 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801666 | ACCAACATGGTGAAA[C/T]CCCACGTCTACTAAA | 254065 |
rs201391121 | in-del | -/CTTA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736706 | AAGTTAAAAAAAAAA[-/CTTA]AGTTGTCAATACAGA | 254065 |
rs201396575 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719688 | ACAAAGCCACAAAAT[C/T]ACTTACATTTTAGTA | 254065 |
rs201400950 | in-del | -/T | 0.103183 | 0.202348 | intron-variant | BRWD3 | GRCh38.p7 | X:80701769 | CAATAATACACGTCA[-/T]TTAAGATATCCTTTA | 254065 |
rs201477283 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721497 | GCCTTAATTCCCTAG[C/T]AATGATATGAAATTC | 254065 |
rs201479064 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684647 | TTGTGCCTTTCTCCT[C/T]CTTGATTTTAAATCA | 254065 |
rs201479814 | in-del | -/CCT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684644 | TGTTTGTGCCTTTCT[-/CCT]TCTTGATTTTAAATC | 254065 |
rs201496334 | snp | C/T | 0.000147901 | 0.00859816 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80676574 | TGCAGTAGAAGGCCA[C/T]TGAATTTTTTAAGTT | 254065 |
rs201501896 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795367 | TACACACACACACAC[-/AT]GTGTATATATACACA | 254065 |
rs201504255 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756385 | TGCATGCCTGTAATC[C/T]CAGCTACTCTGGAGG | 254065 |
rs201506003 | in-del | -/A | 0.0709308 | 0.174454 | intron-variant | BRWD3 | GRCh38.p7 | X:80746205 | AAGAGTAATACAAGT[-/A]AAAAAAAAACTATAC | 254065 |
rs201506984 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779216 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCGC | 254065 |
rs201512337 | snp | A/G | 5.36394e-05 | 0.0051785 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809286 | GACTGCAAGAACCTA[A/G]CGATCAGGTAATACA | 254065 |
rs201529579 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701348 | AGGTCAGGAGTTCGA[C/G]ACCAGCCTGGCCAAC | 254065 |
rs201532245 | in-del | -/C | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80723329 | GACCAATTAAGTTAG[-/C]TCCCAAAGTATTTCA | 254065 |
rs201624879 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80808897 | ACCCCGGTGACAACA[G/T]CTACGGGTACCCAGA | 254065 |
rs201683302 | snp | A/G/T | 0.000269762 | 0.0116111 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791939 | AGACCCATTCCATAG[A/G/T]GTACTCTTACAGTCT | 254065 |
rs201684596 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742407 | GGGCTCTTTTTTGGT[A/T]CTGTAGTTTTTTCCA | 254065 |
rs201687674 | in-del | -/ATT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751982 | ATTTATTCATATTTC[-/ATT]ATTATTATTATTATT | 254065 |
rs201688196 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80682455 | AAATGTTGCATCAAT[A/G]TAATGATACCTAGGT | 254065 |
rs201707054 | in-del | -/AAC | 0.0245906 | 0.108123 | intron-variant | BRWD3 | GRCh38.p7 | X:80726086 | ACATGTTGTCTGTAT[-/AAC]AACATGTTTACATGT | 254065 |
rs201724205 | in-del | -/TGTCTATATAACACAACATGTTTACATGT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726048 | CATGTTTACATGTTA[lengthTooLong]TGTCTGTATAACAAC | 254065 |
rs201752329 | in-del | -/TTTTA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700356 | ACAAAACTGGTCATA[-/TTTTA]AAGTATATGTGCCCC | 254065 |
rs201760320 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727584 | CATGTAGAGGCAGGG[A/T]ATAAACAAGAAAACA | 254065 |
rs201773230 | snp | A/G/T | 0.000190935 | 0.00976904 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80690088 | ACATTAATGCTGATA[A/G/T]TCTCCTGTGAAAGAA | 254065 |
rs201777490 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80736008 | CTTCATTGTTTTTAC[A/G]TGCCATTGCCAGAAA | 254065 |
rs201840669 | in-del | -/A | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80720203 | CTCCTTTTAATTATT[-/A]AAAAAAAATTGCACT | 254065 |
rs201857958 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744301 | GAAGCAGAAATTCAC[A/C]ATACCCCCACCCAAA | 254065 |
rs201910124 | snp | A/T | 0.000273492 | 0.0116906 | intron-variant | BRWD3 | GRCh38.p7 | X:80692005 | ATAAAAAAAAAAAAA[A/T]TAGAAAAAATTATTT | 254065 |
rs201917684 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742402 | AATGTGGGCTCTTTT[A/T]TGGTTCTGTAGTTTT | 254065 |
rs201940083 | in-del | -/T | 0.0147244 | 0.0845304 | intron-variant | BRWD3 | GRCh38.p7 | X:80777398 | GTGGTATTATTATTA[-/T]TTTTTTCTTTTTGAG | 254065 |
rs201943370 | in-del | -/T | 0.0307697 | 0.120159 | intron-variant | BRWD3 | GRCh38.p7 | X:80741689 | TTTCTCATGTGTCTC[-/T]TGGCTGCATAAATGT | 254065 |
rs201954208 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765640 | TGTGTGTATAAAACA[G/T]TTTCTTTGCTTTCCT | 254065 |
rs201976358 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801434 | TCTTGGCCAGGCTGG[A/T]CTTGAACTCCTGACC | 254065 |
rs201980709 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80691820 | TTTTCACATTCATCA[C/T]ACCCAGGGAAAGAAG | 254065 |
rs202007432 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796134 | TAATCAATGTTTTTG[-/T]TTTTTTTTTTTTTTG | 254065 |
rs202054112 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772618 | ACTTAAAGTATAATT[A/T]AAAAAAAAATAAATG | 254065 |
rs202083349 | snp | A/G | 0.000301575 | 0.0122759 | intron-variant | BRWD3 | GRCh38.p7 | X:80733437 | CATTTGTTTACACAA[A/G]TATGTATTACATAAT | 254065 |
rs202096136 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80692157 | TTGTCCCAGCTATTA[A/C]AAAATAAGAAGATGC | 254065 |
rs202159461 | in-del | -/CCAGAG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80794429 | AGGATCACTTGAGCC[-/CCAGAG]GCAGAGGTTGCAGTG | 254065 |
rs202164402 | in-del | -/GGA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721277 | CAAGAAATGTACAAG[-/GGA]AAATAAAGTCTGATA | 254065 |
rs202196546 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795354 | TTGTGTATATATATA[C/T]ACACACACACACATG | 254065 |
rs202197853 | snp | A/G/T | 6.59832e-05 | 0.00574352 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728754 | ATAAAATACTTACAG[A/G/T]TAATGTATGAAGAAG | 254065 |
rs202207027 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688995 | TTTCATGAAAAAAAT[A/T]AAAAAAAACAGCATT | 254065 |
rs207478483 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722259 | TATAAAAGCTTTTAC[A/T]ACAACTCCATACTAT | 254065 |
rs207478484 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734786 | AGTGTTTTCAATATG[A/G]AGCAACAGTACATGT | 254065 |
rs267606518 | snp | A/G | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677282 | TTTTCATCTTCTTCT[A/G]ATGCACTAAGTAGTT | 254065 |
rs367544498 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720458 | TTAAAAATAGAAAAA[C/T]CTTATAGCATAAGGA | 254065 |
rs367609034 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705646 | AGCTATTCTATATAG[G/T]TAGAACCTAATGCTC | 254065 |
rs367619082 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788872 | CTACCTGATTTAATT[C/T]AGATGACATTTTAAA | 254065 |
rs367764579 | snp | A/G | 2.4906e-05 | 0.00352879 | intron-variant | BRWD3 | GRCh38.p7 | X:80722539 | GGCAAAATGTTTTAA[A/G]TTTACTTTTAGAGAA | 254065 |
rs367851913 | snp | A/G | 4.59617e-05 | 0.00479361 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704744 | ATTTTCCTCATCAGA[A/G]CTGCTGCATATTTTA | 254065 |
rs367988595 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757644 | TCTCTTAGATATTTG[A/T]ATTTAAAATTCCATA | 254065 |
rs368052420 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734725 | AAGGAAAAAAAAAAA[-/A]GGTTAACTAATGTAG | 254065 |
rs368054825 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805829 | AGTCCCAGCTACTTG[C/G]GAGGCTGAAGCAGGA | 254065 |
rs368072599 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766703 | GTGATCGATGCAGAA[G/T]ATGGGTGATTTCTGC | 254065 |
rs368093919 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669786 | AAAATGAATAAGCTC[A/C]ATCAATTAATATTAG | 254065 |
rs368125089 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697336 | TGTTTTTGTTTTACT[A/T]CAGATTCATGGGGTA | 254065 |
rs368125780 | snp | C/T | 4.74153e-05 | 0.00486882 | intron-variant | BRWD3 | GRCh38.p7 | X:80723884 | CCTTCAATCTGAAAT[C/T]CAGAGGAGTCTCAAG | 254065 |
rs368149511 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727679 | AAGACTAGGAGGCTA[C/T]CTTGGATTGTTTGAT | 254065 |
rs368153475 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80713213 | AGCTCATTGAGAACG[C/G]GCCATGATGACAATG | 254065 |
rs368161323 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777155 | AAGACCCCCCCCCAC[A/G]AAAAACCTCCTGAGC | 254065 |
rs368173923 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800768 | AAAAAAAGAAAAAAA[-/A]GACAGCAGGCAGGCC | 254065 |
rs368237825 | snp | C/G | 0.00010191 | 0.00713753 | intron-variant | BRWD3 | GRCh38.p7 | X:80709385 | GATGATACAAACTGG[C/G]AAACAAAAAACTACA | 254065 |
rs368306499 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80683850 | AGAGTAAAGAGACAA[A/G]TAAGAGAAAGGAAAA | 254065 |
rs368427489 | snp | C/T | 4.57258e-05 | 0.0047813 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682021 | AGAAAGGAGAGCTAG[C/T]CCTGGCATGAGATAC | 254065 |
rs368487981 | snp | C/T | 0.00032393 | 0.0127224 | intron-variant | BRWD3 | GRCh38.p7 | X:80689927 | TTAATTTTTTAAAAA[C/T]CTTAAGTTAGACTCT | 254065 |
rs368533620 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80780336 | TTAAATGGAGAAAAT[A/G]CTTTTTTCATTATAT | 254065 |
rs368543370 | snp | A/G | 0.000189982 | 0.00974449 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80725062 | GAATACTTCATCATC[A/G]TGTCCCTATAATAAA | 254065 |
rs368569131 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739179 | TTGCCAGATTCTAGA[C/T]ACACTTTGATGGTAG | 254065 |
rs368599090 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80727058 | CCTTAGGAGAGTACA[C/T]AGTTACTAGATCATG | 254065 |
rs368605172 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785953 | GAGAATCACTTGAAC[A/C]CAGAAGCGGGGGTTG | 254065 |
rs368605872 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708598 | AGGTGGGCAGATCAC[C/T]TGAGGTCAAGAGTTC | 254065 |
rs368638633 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80751083 | AGAAAGGTAGTTACC[A/C]CAGGATACAAGGAAA | 254065 |
rs368728839 | in-del | -/GGG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80808761 | GCTAGACAAGTATAT[-/GGG]GGGGGGGGGGAAGGG | 254065 |
rs368767975 | snp | C/T | 0.000718907 | 0.0189456 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793572 | TCTAAAAATAAGCTA[C/T]TCTCCACTCCTTCCT | 254065 |
rs368790001 | snp | A/T | 0.0126344 | 0.0784702 | intron-variant | BRWD3 | GRCh38.p7 | X:80719332 | TTTATCCACAAATGA[A/T]GAGATTATGAGACTT | 254065 |
rs368799965 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789611 | TCGATCTCCTGACCT[C/T]GTGATCCACCCACCT | 254065 |
rs368861463 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711904 | AATCCAACCAGTAGC[C/T]TGGCCATCTTAGGCA | 254065 |
rs368871624 | snp | A/G | 0.000392157 | 0.0139973 | intron-variant | BRWD3 | GRCh38.p7 | X:80728741 | AATTACTCTAAAAAT[A/G]AAATACTTACAGATA | 254065 |
rs368924482 | snp | A/G | 0.0014754 | 0.0271206 | intron-variant | BRWD3 | GRCh38.p7 | X:80703624 | ACGAAAAGTATATGT[A/G]TAAAACACAGTTCTC | 254065 |
rs368937821 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757929 | AAATAGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 254065 |
rs368951042 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant | BRWD3 | GRCh38.p7 | X:80693068 | TATAATGTTTTAAAA[C/T]TCTTAAAAGGATGCT | 254065 |
rs368965655 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763109 | TTAATGATTTTTATA[C/T]GCCAGGCACTATTCT | 254065 |
rs368967780 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809520 | GGAGGGGCTGGCGGG[A/G]GCGGGTGGGGGCGCT | 254065 |
rs369118921 | snp | C/T | 0.000296364 | 0.0121694 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717620 | CACTCTTCTGCTCCA[C/T]GCCATGAGATCTCTT | 254065 |
rs369153163 | in-del | -/TCT | | | cds-indel, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677273 | CCTCCCATGTTTTCA[-/TCT]TCTTCTGATGCACTA | 254065 |
rs369163037 | snp | C/G | 4.64743e-05 | 0.00482027 | intron-variant | BRWD3 | GRCh38.p7 | X:80808623 | GGACGAAAAGAAAGG[C/G]GGAAGCGGAGGCAAA | 254065 |
rs369226496 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80759772 | TGATAGCTATAATTG[A/G]AGTGTGGAGGGGAAG | 254065 |
rs369228468 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722925 | TTGTTGCCCTGTATT[C/T]CCTTTAGGTAGAAGA | 254065 |
rs369239176 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810658 | GTATTATTGCCTATC[G/T]CTATGCAAGGTATCA | 254065 |
rs369269350 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732668 | GTATAAGCAAAGGAA[C/T]GGATGAGATGTGAAC | 254065 |
rs369278963 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767501 | AACAAACAACAAGGA[A/C]TAGCATCAACATCAA | 254065 |
rs369328692 | snp | C/T | 4.56251e-05 | 0.00477603 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682527 | TTTTCTGTACCGTGG[C/T]CTTCTCCTCTTCTGA | 254065 |
rs369334946 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673231 | GCATCTGCGGGAAAC[A/G]AAGTATTATAGAGAA | 254065 |
rs369343000 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781725 | CCAACAGAGCACAAT[A/G]TGAAAAGGAAATCAA | 254065 |
rs369363210 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708558 | CAGTGGCTCACGCCT[A/G]TAATCCTAGCACTTT | 254065 |
rs369366827 | snp | C/T | 2.51086e-05 | 0.00354312 | intron-variant | BRWD3 | GRCh38.p7 | X:80729892 | ATCATGAGAACCACA[C/T]AAACATCTAACATAT | 254065 |
rs369368128 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80752763 | CAACCTCCACCTCCC[A/C]GGTTCAGGCTCCTGC | 254065 |
rs369387520 | snp | C/G | 0.0704399 | 0.173949 | intron-variant | BRWD3 | GRCh38.p7 | X:80712337 | TATTTTTTTGGTGGA[C/G]ACGGGGTTTCGCTGT | 254065 |
rs369397955 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715067 | TTAAAAGTGTATGTA[A/T]ATGTTTCACATTTTC | 254065 |
rs369469570 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766993 | GAATCCCAAGCCCAC[C/T]AAGCCTTGCTTACTG | 254065 |
rs369520008 | snp | C/G | 2.4241e-05 | 0.00348136 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80684156 | TATCTATAACATCTT[C/G]ATAATCCTACAAAGA | 254065 |
rs369625932 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80728674 | TATCATAGAAAGGAA[A/C]CTGGAACTTAAATTT | 254065 |
rs369647950 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782442 | CTCTCCAGGACATTG[A/G]ACTGGGTAAGGATTT | 254065 |
rs369697526 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676330 | GTGTCTGTGTTGTGT[G/T]TCGTGTGTGTGTGTC | 254065 |
rs369732154 | snp | A/G | 0.000189982 | 0.00974448 | intron-variant | BRWD3 | GRCh38.p7 | X:80808999 | TCCCCACCCTTCCCG[A/G]AGGGGCTCCGTACCT | 254065 |
rs369789389 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant | BRWD3 | GRCh38.p7 | X:80734097 | TCAAAAATAAAGCAA[C/T]CGTTTCTGATTTTCT | 254065 |
rs369807002 | snp | A/G/T | 2.40315e-05 | 0.00346629 | intron-variant | BRWD3 | GRCh38.p7 | X:80692178 | AAGAAGATGCAAATC[A/G/T]AATTAATCATATAGT | 254065 |
rs369838172 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767260 | CTCAAGAGGTTCCCT[C/G]ACCCCTGTGTAGCCT | 254065 |
rs369928663 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762994 | GAATAGTGATCGCTA[C/G/T]TATAAAGAAAATAAA | 254065 |
rs369954231 | snp | A/C | 0.00475684 | 0.0485365 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671638 | TGAAGATAATTGCTT[A/C]TAATGACTGATAACT | 254065 |
rs370074431 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746583 | ATCTTCCCTTATACA[C/T]TAAAAGTGCTTAACA | 254065 |
rs370098516 | snp | A/G | 2.30497e-05 | 0.00339475 | intron-variant | BRWD3 | GRCh38.p7 | X:80686841 | ATCATACTGACAATT[A/G]TTTAAACAACTGTAT | 254065 |
rs370127946 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80690672 | CTCCTTTCCTGTATA[A/T]ATTTCAGTGCTGGTA | 254065 |
rs370151594 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796510 | TGTTTTCCTAGGAAA[A/C]ACAGGTCAAAGAACC | 254065 |
rs370152001 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80760574 | TGCACTGGAATATTA[C/T]TCACATATTTAAATT | 254065 |
rs370178724 | snp | A/G | 3.14886e-05 | 0.00396779 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704654 | AAAAATAACAAAAAC[A/G]AAATAACTTATAAAG | 254065 |
rs370241837 | snp | C/T | 2.30518e-05 | 0.00339491 | intron-variant | BRWD3 | GRCh38.p7 | X:80681296 | ATTTATCTGCTATCA[C/T]AAAGAAATAAATAAT | 254065 |
rs370277579 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733595 | AACATCATGAAGTAG[-/T]TTTTTTTTTTTTTTA | 254065 |
rs370332815 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712941 | TGAGAAGTGAGGAGC[C/T]CCTCCGCCCGGCACC | 254065 |
rs370347131 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776271 | AAGATGGTCACATCA[C/G]AGTTGTTAGACCACT | 254065 |
rs370398878 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746075 | ATGAAGAAATTTTAG[A/G]ATAAAACTGTACTTG | 254065 |
rs370428229 | snp | A/G | 0.00019998 | 0.0099975 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809461 | TCGATCTGGGTAGGT[A/G]CTGCCGCCATCCTTT | 254065 |
rs370443489 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80694484 | ACCGACAACGTGCGC[C/T]GTGTGCCTGGAAAAG | 254065 |
rs370550527 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708586 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACCTGA | 254065 |
rs370580962 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670128 | GTTACATAGAAAGGA[A/C]AGGAAAATGTTTCCC | 254065 |
rs370591157 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726054 | TACATGTTATGTCTA[C/T]ATAACACAACATGTT | 254065 |
rs370593341 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80713218 | ATTGAGAACGGGCCA[C/T]GATGACAATGGCGGT | 254065 |
rs370648386 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703849 | AAACCATAACTTTTA[A/C]ATACGTCCCTTGACT | 254065 |
rs370653262 | snp | A/C/G | 0.000297643 | 0.0121958 | intron-variant | BRWD3 | GRCh38.p7 | X:80688047 | AAAACATATCTCCTC[A/C/G]GCAGTTCACTTATTT | 254065 |
rs370726397 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80717827 | TTCCAGAACAGAGCT[A/C]TAAATAAAACAGTAG | 254065 |
rs370728871 | snp | A/G | 8.84395e-05 | 0.0066492 | intron-variant | BRWD3 | GRCh38.p7 | X:80689876 | ATTTCAAAAGCTTCA[A/G]TAATTTTTACAATTT | 254065 |
rs370732682 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681678 | TCAGAAAAACTTGTC[C/G]AATTGCTCATCATAA | 254065 |
rs370752153 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708607 | GATCACCTGAGGTCA[A/G]GAGTTCAAGATCAGC | 254065 |
rs370753868 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755554 | CCATACAGTGAGATG[A/T]TCCCTTAGGAAAATA | 254065 |
rs370857816 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803100 | GCGCAAGACTCCATC[G/T]CAAAAAAAAAAAAAA | 254065 |
rs370882636 | in-del | -/AAAA | 0.155165 | 0.231314 | intron-variant | BRWD3 | GRCh38.p7 | X:80720569 | AACAAACAAACAAAC[-/AAAA]AACCAAAAAACCTAA | 254065 |
rs370940321 | snp | A/T | 6.48078e-05 | 0.00569207 | intron-variant | BRWD3 | GRCh38.p7 | X:80700082 | AAAACAGAAAACATA[A/T]GGTATTAAACAGCAG | 254065 |
rs370975126 | snp | A/G | | | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704628 | ATTTAAGTTATCAAA[A/G]GCAAAAAACAAAAAA | 254065 |
rs370986701 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768850 | CAACTCAGGTGCAGA[A/G]ACACACATAGGCTCA | 254065 |
rs371032852 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811512 | CAAAGTCTTGACTGC[C/T]TTTTGACTGTGATCC | 254065 |
rs371044988 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754746 | GCATGGTGGCTCACG[C/T]CTATTATCCCAGCAC | 254065 |
rs371074790 | snp | A/G | 0.299416 | 0.245067 | intron-variant | BRWD3 | GRCh38.p7 | X:80712668 | TGGAAAGTGAGGAGC[A/G]TCTCTGCCCAGCCGC | 254065 |
rs371100123 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756270 | ACTTTGGGAGGGTGA[A/G]GTGGGCAGATCACCT | 254065 |
rs371103718 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80718942 | TTTAAGGATAGAATA[C/T]TCATTTTAAGATAAT | 254065 |
rs371107698 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788379 | ACTCTCAAAACTCAA[C/T]AATAAAAAAACGCAA | 254065 |
rs371120641 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795533 | TATACATATATGTGT[A/G]TATATATATGCCATT | 254065 |
rs371135346 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692135 | GCTCATCTTTTCTCT[C/T]TCATTATTGTCCCAG | 254065 |
rs371149829 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708592 | AGGCCAAGGTGGGCA[G/T]ATCACCTGAGGTCAA | 254065 |
rs371172563 | in-del | -/AACT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695138 | GGCACTTCCACTTCT[-/AACT]CTCTGTCTCCTGCAG | 254065 |
rs371311938 | snp | C/T | 2.31613e-05 | 0.00340296 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793577 | AAATAAGCTACTCTC[C/T]ACTCCTTCCTCTGAT | 254065 |
rs371317961 | snp | G/T | 7.0748e-05 | 0.00594719 | intron-variant | BRWD3 | GRCh38.p7 | X:80682129 | ACAACGAGCATTTTT[G/T]TTTTTCTGTTAGCAA | 254065 |
rs371334335 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756530 | AAAAAAAAAAAGAAA[A/C]AATGTCAACACTCTC | 254065 |
rs371447937 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715274 | AATAAAGTTAATTTC[A/T]TAACAATAAAAGTTA | 254065 |
rs371476187 | in-del | -/AAAG | 0.000540687 | 0.0164332 | intron-variant | BRWD3 | GRCh38.p7 | X:80730389 | AAATATTATTTAGCA[-/AAAG]AAAGAAAGAAAGAAA | 254065 |
rs371489448 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80713638 | CCTCCACTATTGTCC[C/T]ATGACCCTGCCAAAT | 254065 |
rs371508015 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant | BRWD3 | GRCh38.p7 | X:80722534 | CATTGGGCAAAATGT[C/T]TTAAATTTACTTTTA | 254065 |
rs371593146 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697337 | GTTTTTGTTTTACTT[C/T]AGATTCATGGGGTAC | 254065 |
rs371717290 | in-del | -/CCT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680709 | GACTTTGGAAACTCT[-/CCT]TTCTTATTAATATGA | 254065 |
rs371742468 | snp | A/C | 2.34425e-05 | 0.00342355 | intron-variant | BRWD3 | GRCh38.p7 | X:80683963 | ACCAATTTTCAGTAA[A/C]TGGTTAAAGAAAACT | 254065 |
rs371870737 | snp | C/T | 0.000123548 | 0.00785868 | intron-variant | BRWD3 | GRCh38.p7 | X:80691192 | CAAAATTATGAAAAT[C/T]AAATAAGGTAGCTAT | 254065 |
rs371898396 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714756 | TCAAAGGCACATAGA[C/T]GCACACAAATTCATG | 254065 |
rs371994257 | snp | A/G | 7.15231e-05 | 0.00597967 | intron-variant | BRWD3 | GRCh38.p7 | X:80723888 | CAATCTGAAATTCAG[A/G]GGAGTCTCAAGTCAT | 254065 |
rs371995435 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727775 | TTAACCCAAACTACA[C/G]TTCCTCAGGAAGTTT | 254065 |
rs372009174 | snp | A/G | 2.28551e-05 | 0.00338039 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682060 | TCTGGTCATTTTTAG[A/G]CTGCAACTTCATTTG | 254065 |
rs372068484 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671049 | CATCTCACCTCACTT[C/T]TCTCTCTCCTACACT | 254065 |
rs372073630 | snp | C/T | 8.839e-05 | 0.00664734 | intron-variant | BRWD3 | GRCh38.p7 | X:80745742 | TCACTGAAAAAAATA[C/T]GAAATTAACTTAAAA | 254065 |
rs372083982 | snp | A/G | 2.37719e-05 | 0.00344752 | intron-variant | BRWD3 | GRCh38.p7 | X:80704884 | GATACCTAAGTATAG[A/G]AAAGGAGTAGTTTTA | 254065 |
rs372146949 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707868 | AAAAATTTTAATTAT[A/C]TTTTTTATGTAAAAT | 254065 |
rs372154658 | snp | C/G | 2.3297e-05 | 0.00341291 | intron-variant | BRWD3 | GRCh38.p7 | X:80808631 | AGAAAGGGGGAAGCG[C/G]AGGCAAATGATGAAG | 254065 |
rs372203281 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758126 | ATTGCTTGAACCTGG[A/G]AGGCGGAGGTTGTGG | 254065 |
rs372250213 | snp | A/G | 0.000494904 | 0.0157228 | intron-variant | BRWD3 | GRCh38.p7 | X:80691005 | AAAAAGGAAAGCAAA[A/G]GCCATAAAGCTATAA | 254065 |
rs372250770 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685850 | TGTAGTAAGCTCATA[A/G/T]GACGGTCTGATGTAT | 254065 |
rs372374523 | snp | C/G/T | 9.48159e-05 | 0.00688481 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692090 | AAAAGCATATTTACT[C/G/T]CCTTCTGGAATTGGC | 254065 |
rs372401297 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767102 | GTAGGTAAACAAAGC[C/T]ACAGGAAGCTTGAAC | 254065 |
rs372487582 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759489 | TGCATTTTCTTTTCT[A/C]TAACTATGCTTGCTC | 254065 |
rs372559820 | snp | C/T | 9.24054e-05 | 0.00679663 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709525 | TGGTAAGTATGCTGA[C/T]GTTTGCGCTGTGTCC | 254065 |
rs372598373 | snp | A/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810271 | GGTTTTGTTTGCTGT[A/T]TATACTCTACCCCGT | 254065 |
rs372613809 | snp | C/T | 0.000189982 | 0.00974449 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728794 | GATAGAATTCCACAC[C/T]TTCAAAAGAAAATTG | 254065 |
rs372620625 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751511 | ATATTTGAGTTCCTT[A/C]ATGGCCAAAGAAACA | 254065 |
rs372639187 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739807 | AATGTTATAAAATTA[C/T]AACAATATACTATAA | 254065 |
rs372645356 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80808431 | TCTTTGGCTCTGCAC[C/G]GAGCTCTAGAACCTC | 254065 |
rs372652251 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784325 | AATTAGGAAAATTCC[C/T]AAAATTGTTACCATG | 254065 |
rs372692876 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701408 | CAAAAATTCACCGGG[C/T]GTGGTGGTGCACGCC | 254065 |
rs372694716 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715588 | GATTTGGTAAGCCAG[G/T]AATGGGTCTAGGGTA | 254065 |
rs372762145 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752675 | GAGCATTTTTTCTTT[C/T]TCTTTCTTTCTTGAG | 254065 |
rs372784514 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779263 | AAGGTTGCAGTGAGT[C/T]GAGATTGTGCCACTG | 254065 |
rs372790076 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80702050 | TAGACCTTGAAAATG[A/G]TAATTTTAAGAAGCA | 254065 |
rs372830273 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698314 | TATATTAGCATATAG[A/C]AAAGCTAGAATTGAA | 254065 |
rs372849771 | snp | C/T | 0.000407732 | 0.0142724 | intron-variant | BRWD3 | GRCh38.p7 | X:80725104 | ACAATGAAAGCAACA[C/T]GAAATGTTTGGTTCA | 254065 |
rs372899207 | snp | C/T | 0.000875625 | 0.0209056 | intron-variant | BRWD3 | GRCh38.p7 | X:80719476 | CACCCTTTACAAGTA[C/T]AAAAATACTTACCAC | 254065 |
rs372933769 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697970 | ACCTCACAAGCATCT[A/G]TTTGTTTGTTTTGAA | 254065 |
rs372990326 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708587 | TTGGGAGGCCAAGGT[A/G]GGCAGATCACCTGAG | 254065 |
rs372993559 | snp | A/G | 2.2925e-05 | 0.00338555 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686903 | TGTCGAAATGGCTCC[A/G]AGTCTTCACGTTCAT | 254065 |
rs373015518 | snp | C/T | 4.7142e-05 | 0.00485477 | intron-variant | BRWD3 | GRCh38.p7 | X:80699919 | ATTTAATTCCAAAGC[C/T]ACTTCCATTGCATAG | 254065 |
rs373042116 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712280 | CAGCCTGCCGAGTGC[C/G]TGTGATTGCAGGCAC | 254065 |
rs373045540 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772673 | AGAAATTAATAATAA[A/C]ACTCTAAGAAACAAA | 254065 |
rs373057322 | snp | A/G | 0.000189982 | 0.00974448 | intron-variant | BRWD3 | GRCh38.p7 | X:80809340 | GAGGTTCAGAGGGAG[A/G]TAGAGAAGAGAAATA | 254065 |
rs373107325 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753318 | CTCGTCACCCAGGCT[A/G]GAGTGCAGTGGTGTG | 254065 |
rs373110888 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715090 | ACATTTTCAACCTAA[A/G]TAAAAATATCTACAG | 254065 |
rs373111895 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754871 | AAATTAGCCAGATGT[A/G]GTGGTATGCACCTGT | 254065 |
rs373112479 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678135 | AGGCAAGACTGAAAG[C/T]GGAAGGAGAGACCAG | 254065 |
rs373201455 | snp | C/T | 0.0058139 | 0.0536018 | intron-variant | BRWD3 | GRCh38.p7 | X:80693392 | GATTCTTCTATCTTG[C/T]TTTTAGCTTTCTTTA | 254065 |
rs373220604 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781897 | CCATATTCATGAATT[A/G]TAAGAATCATTATTG | 254065 |
rs373239185 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80741751 | CGCCTACTTTTTGAC[A/G]GGGTTGTTTGTTTTT | 254065 |
rs373283036 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80712678 | GGAGCGTCTCTGCCC[A/G]GCCGCCATCCCATCT | 254065 |
rs373289070 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80743901 | TCTTGCTGCAGGGTA[C/G]GAGCAAAGTCCAGAA | 254065 |
rs373300765 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775917 | GTAGTCTTGTGAGAT[C/T]TGAAGGCAAGTTTCT | 254065 |
rs373305366 | snp | A/G | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811648 | GTTTGACCTGTATGT[A/G]ACAGTTAACACTTAA | 254065 |
rs373393872 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730318 | AAAAGTGGAAACAAC[C/G]CAAATGTCCATCAAC | 254065 |
rs373434889 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708565 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 254065 |
rs373574084 | snp | A/T | 0.0014486 | 0.0268739 | intron-variant | BRWD3 | GRCh38.p7 | X:80722538 | GGGCAAAATGTTTTA[A/T]ATTTACTTTTAGAGA | 254065 |
rs373681832 | in-del | -/A | 0.185696 | 0.241589 | intron-variant | BRWD3 | GRCh38.p7 | X:80750385 | AATAGCAAAAAAAAA[-/A]TGTAATTAAAAATGG | 254065 |
rs373686108 | snp | A/T | 3.03984e-05 | 0.00389849 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745703 | AGCGACTACAGCCGG[A/T]TAATTGCCTGGCAGA | 254065 |
rs373703816 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689047 | TTAACGGTATAAATA[A/G]TATAAACATGCAAAA | 254065 |
rs373744280 | snp | G/T | 0.000189982 | 0.00974449 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719620 | TCTTGGTCATTGGTT[G/T]GCTGCCCAATTACCT | 254065 |
rs373765583 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80704992 | AAAAATATCATCCAG[G/T]CACGGTGGCTCACAC | 254065 |
rs373775652 | in-del | -/CTCAAAAAAAAAAAAAAAAAAAAAAAAGAAA | 0.0630423 | 0.165972 | intron-variant | BRWD3 | GRCh38.p7 | X:80803099 | AGCGCAAGACTCCAT[lengthTooLong]TGTCAAGCAAGGGCA | 254065 |
rs373782230 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793539 | AGTATTTAGAAAAGC[A/C/T]TGGGAACATTTACTC | 254065 |
rs373793958 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804349 | CTCAAGCAATTCTCA[C/T]GCCTCAGCCTCCTGA | 254065 |
rs373848488 | snp | A/G | 6.88192e-05 | 0.00586557 | intron-variant | BRWD3 | GRCh38.p7 | X:80734099 | AAAAATAAAGCAACC[A/G]TTTCTGATTTTCTCT | 254065 |
rs373913543 | snp | C/G | 0.000160267 | 0.00895031 | intron-variant | BRWD3 | GRCh38.p7 | X:80688049 | AACATATCTCCTCAG[C/G]AGTTCACTTATTTAC | 254065 |
rs374095212 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769372 | GCAAATGTAAAAGAA[A/C]ACAAATTATAACAAA | 254065 |
rs374172860 | snp | G/T | 0.000379928 | 0.0137775 | intron-variant | BRWD3 | GRCh38.p7 | X:80691038 | TTTATAATAAGTGAT[G/T]AAAAAAAAACAGACC | 254065 |
rs374190987 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700433 | AGATTGAAAATATTT[-/G]ATATATATAACAATA | 254065 |
rs374235616 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776700 | ATGAAGACTCCCTCT[C/T]GAGTGATTACTGCTT | 254065 |
rs374242886 | snp | A/G | 2.94053e-05 | 0.00383429 | intron-variant | BRWD3 | GRCh38.p7 | X:80685425 | GTTTAGAAAGTAAAA[A/G]CAATCAATATGTCTT | 254065 |
rs374260917 | snp | C/G | 0.00171925 | 0.0292689 | intron-variant | BRWD3 | GRCh38.p7 | X:80809080 | TATGAGGAGCAGCTC[C/G]GGCCATCAACCCATT | 254065 |
rs374261575 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733627 | TTTCAATGAAGCCCA[A/G]AACAATGTACTAACT | 254065 |
rs374278526 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703958 | AAAAGACTATAGAAT[A/G]TGTCTATAATCAATT | 254065 |
rs374340324 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80713178 | CCCGGCCACCACCCC[A/G]TCTGGGAGGTGTACC | 254065 |
rs374423759 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | BRWD3 | GRCh38.p7 | X:80758140 | GGAGGCGGAGGTTGT[A/G]GTGAGCCAAGATCGC | 254065 |
rs374430034 | snp | A/C | 3.41116e-05 | 0.00412973 | intron-variant | BRWD3 | GRCh38.p7 | X:80689886 | CTTCAGTAATTTTTA[A/C]AATTTTTCAATTAAT | 254065 |
rs374464283 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707784 | AATATAACCCTCTTA[A/G]ATACATTAGAAACAT | 254065 |
rs374496429 | snp | C/T | 9.97855e-05 | 0.00706277 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791936 | AGCAGACCCATTCCA[C/T]AGTGTACTCTTACAG | 254065 |
rs374506452 | snp | A/G/T | 0.000442896 | 0.0148751 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703531 | GGGTATAGTATCCAA[A/G/T]ATCCACTGAGGGGCA | 254065 |
rs374506776 | snp | A/G | 6.88342e-05 | 0.0058662 | intron-variant | BRWD3 | GRCh38.p7 | X:80682101 | CCTTTTGGACTAGAA[A/G]TAAAAATATGTAACA | 254065 |
rs374518563 | snp | C/T | 2.83523e-05 | 0.00376502 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704665 | AAACAAAATAACTTA[C/T]AAAGTTACAAACCTT | 254065 |
rs374537740 | snp | G/T | 2.31887e-05 | 0.00340497 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676908 | TTCCCCTCCCCCTAG[G/T]GCCACCTCCACCTCT | 254065 |
rs374553482 | snp | C/T | 7.22335e-05 | 0.00600929 | intron-variant | BRWD3 | GRCh38.p7 | X:80692181 | AAGATGCAAATCAAA[C/T]TAATCATATAGTACT | 254065 |
rs374749055 | snp | G/T | 9.43641e-05 | 0.00686827 | intron-variant | BRWD3 | GRCh38.p7 | X:80808524 | AGGTTAAGTTGAAAT[G/T]AAAACTTTACTCACC | 254065 |
rs374753047 | snp | C/T | 4.56345e-05 | 0.00477652 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682472 | AATGATACCTAGGTG[C/T]TCCACTACTAGATAA | 254065 |
rs374818711 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678148 | AGTGGAAGGAGAGAC[C/T]AGTTGGGCATCCACT | 254065 |
rs374822657 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766306 | GGACAGGATCTTATA[C/T]CACCAGCTTTCCTGG | 254065 |
rs374823461 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80686647 | GCAAATGAATTCTGA[C/T]TTAAATTTTTGTTTT | 254065 |
rs374894088 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751779 | ACATCCAGATGTCCA[C/T]ATTTTGTAGCACCCA | 254065 |
rs374924230 | snp | A/G | 2.57241e-05 | 0.00358628 | intron-variant | BRWD3 | GRCh38.p7 | X:80729882 | TGTAAAATATATCAT[A/G]AGAACCACATAAACA | 254065 |
rs374940665 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750892 | CACACACACACACAC[A/G]CGCAAAAATCATTAA | 254065 |
rs374951705 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805008 | AACTGACCAAAATGC[C/T]TCATCATGTACAGAT | 254065 |
rs374958094 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756656 | TTAATGGTTGATAAT[C/T]GATTATACAGATACA | 254065 |
rs374965939 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803129 | AAAAAAAAAAAAGAA[A/T]TGTCAAGCAAGGGCA | 254065 |
rs374994843 | snp | A/G | 9.14516e-05 | 0.00676147 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681430 | TATCCACCGAAGCTC[A/G]ATGAAGAAAATGGCC | 254065 |
rs375004561 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720405 | GTATGTTTGTGTCTT[A/C]ACTTTTAAAAAGTTT | 254065 |
rs375027477 | snp | A/G | 7.50234e-05 | 0.00612422 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80736044 | TGTTCCATCAGCACC[A/G]GTAGAAGTGAGGTAT | 254065 |
rs375029296 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722900 | ATCTTTTGCATACTC[G/T]TCTAGTCCTTTGTTG | 254065 |
rs375030313 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687728 | GCTAGTCAGAGGGTA[C/T]CTACATAACCAGCCC | 254065 |
rs375035629 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759003 | TACTTTCTTCTGGGA[A/G]GTCTCTAGTTTATCA | 254065 |
rs375054450 | snp | A/G | 9.15594e-05 | 0.00676545 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682001 | GACATATTTACCAGG[A/G]GATGAGAAAGGAGAG | 254065 |
rs375065101 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718404 | ATATTACAAATAGAA[G/T]TCAGTGGGGTCTCTT | 254065 |
rs375073538 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755575 | TAGGAAAATAACTTG[A/G]CAATATACTTGAAGA | 254065 |
rs375087107 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719090 | TCAAGAGAAGAGCAT[A/G]GTATTCTGCTTTCCT | 254065 |
rs375089932 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792887 | CAATTACTGAGGCCC[A/G]GCGCAGTGGTTTACG | 254065 |
rs375093976 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700431 | GCAGATTGAAAATAT[A/T]TGATATATATAACAA | 254065 |
rs375161842 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768338 | AGAGAGAGAAAGGTC[A/G]AGTTACCCACAAAGA | 254065 |
rs375169797 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80714752 | TTCGTCAAAGGCACA[C/T]AGACGCACACAAATT | 254065 |
rs375201449 | snp | A/G | 2.30585e-05 | 0.00339539 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723820 | TGTGCAGGCAAAATG[A/G]TTTCCATCTGGTGAA | 254065 |
rs375217103 | snp | A/G | 0.000140164 | 0.00837033 | intron-variant | BRWD3 | GRCh38.p7 | X:80691799 | CTCTTGCATGCTCCT[A/G]AAATTTTTTCACATT | 254065 |
rs375284158 | in-del | -/A | 0.173397 | 0.237975 | intron-variant | BRWD3 | GRCh38.p7 | X:80734715 | ACAATCAAAAAAAGG[-/A]AAAAAAAAAAGGTTA | 254065 |
rs375347676 | snp | C/T | 0.000434322 | 0.01473 | intron-variant | BRWD3 | GRCh38.p7 | X:80808991 | CTCAACCCTCCCCAC[C/T]CTTCCCGAAGGGGCT | 254065 |
rs375400617 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80726929 | GGTTCCTAACCAGCA[A/G]AACATAAAGTTAGTT | 254065 |
rs375499745 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80689084 | ATGCCACTGCAACAC[A/G]ATCTAGCATATGTGA | 254065 |
rs375552459 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80798677 | GTGGCTCACGCCTGT[A/C]ATCTCAGCACTTGAG | 254065 |
rs375588857 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80789406 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 254065 |
rs375613891 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722340 | ATACATTATCTGCTT[A/G]ATGCTTATGTTTGTC | 254065 |
rs375703335 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745215 | CATTATTTAGGGAAA[A/C]CTGGCAGCAATTACA | 254065 |
rs375704347 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670170 | GGGAAAAATCGATAC[C/T]GTAAAAAGTTTACTT | 254065 |
rs375714071 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80713330 | CATGGGAGACTTTTC[A/G]TTTTGTTCTGTACTA | 254065 |
rs375731642 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708593 | GGCCAAGGTGGGCAG[A/G]TCACCTGAGGTCAAG | 254065 |
rs375830120 | snp | A/G | 2.32553e-05 | 0.00340985 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709537 | TGACGTTTGCGCTGT[A/G]TCCTGCGTAAAGAAC | 254065 |
rs376078579 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755156 | TTGCATCTCTGGTAT[A/G]TTATCTTTTAGCTGT | 254065 |
rs376137184 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712573 | GCCCGGCCGCCACCC[C/T]GTCTGGGAAGTGAGG | 254065 |
rs376185763 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724675 | GGTTAGGTGTTAACT[C/T]CAAAGCTTAATACAT | 254065 |
rs376204666 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793610 | CACAGTCCTAAATTC[C/T]GAAAATCTCACCTTT | 254065 |
rs376227492 | snp | A/T | 2.29009e-05 | 0.00338377 | intron-variant | BRWD3 | GRCh38.p7 | X:80688045 | TGAAAACATATCTCC[A/T]CAGCAGTTCACTTAT | 254065 |
rs376250330 | snp | C/T | 0.000109571 | 0.00740091 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80700044 | AACATAAGCTTCATG[C/T]CCTTGCCTAAAATAG | 254065 |
rs376282980 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80741195 | ATAGTTTGCAGAGAA[C/T]GATGGTTTCCAGCTT | 254065 |
rs376289604 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680973 | CATGTGGCTACTTTT[-/A]TTTTTTTTTTTTTTT | 254065 |
rs376330443 | in-del | -/T | 0.00134267 | 0.0258753 | intron-variant | BRWD3 | GRCh38.p7 | X:80682124 | ATGTAACAACGAGCA[-/T]TTTTTTTTTTCTGTT | 254065 |
rs376361976 | snp | A/G | 4.68516e-05 | 0.00483979 | intron-variant | BRWD3 | GRCh38.p7 | X:80683966 | AATTTTCAGTAACTG[A/G]TTAAAGAAAACTGCC | 254065 |
rs376412799 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80776011 | TCAAAAAATAGCAGA[A/G]GCTCAATCTAGGTCT | 254065 |
rs376429247 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80723314 | CTAATAAAACATAAA[A/G]ACCAATTAAGTTAGC | 254065 |
rs376461143 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708575 | AATCCTAGCACTTTG[A/G]GAGGCCAAGGTGGGC | 254065 |
rs376495287 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783552 | GGACTACCATATAAT[C/T]CAGTGATCCTACTGC | 254065 |
rs376499394 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733789 | TAATATAAGAGAATA[A/C]CTTAAAATAGTTAAT | 254065 |
rs376501012 | snp | C/T | 0.000171407 | 0.00925603 | intron-variant | BRWD3 | GRCh38.p7 | X:80723912 | AAGTCATCTTAAGAG[C/T]AATTTTCAAATAATA | 254065 |
rs376505660 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant | BRWD3 | GRCh38.p7 | X:80696708 | ATTAAAATACACACA[C/T]TCAAACAGAGACTCA | 254065 |
rs376547361 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697411 | TTGAGTTTCTAGTGT[A/G]CCCATCCTCCAAATA | 254065 |
rs376573279 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740417 | CCACTATGTGGACAA[C/T]TATTAAAAGAAGCCA | 254065 |
rs376579835 | in-del | -/CAA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80682201 | CAGGTATTAGCTGGC[-/CAA]AGAAGAAATGCCCTA | 254065 |
rs376669673 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80694929 | GTTTTGAAATGAGAA[C/T]ATGAGATTTGGGAGG | 254065 |
rs376683434 | snp | G/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811396 | ATATTTCAGCTATAG[G/T]ACCCAAGTCTAAATT | 254065 |
rs376818035 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722367 | GTCCTAACCCACTTA[-/A]TCTGTGTCCAGGTGA | 254065 |
rs376879215 | snp | C/G | 0.000876177 | 0.0209122 | intron-variant | BRWD3 | GRCh38.p7 | X:80809327 | AGAGGGGGGAAAAGA[C/G]GTTCAGAGGGAGGTA | 254065 |
rs376899514 | snp | A/G | 0.000117876 | 0.0076762 | intron-variant | BRWD3 | GRCh38.p7 | X:80716109 | AAGCCTATTATCTAC[A/G]AATATCTGCAAATAG | 254065 |
rs376909976 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80784483 | TGCTGCACTTAACCC[A/G]TCACCTAGGTATTGA | 254065 |
rs376951768 | snp | C/T | 2.57945e-05 | 0.00359118 | intron-variant | BRWD3 | GRCh38.p7 | X:80722522 | AGTAATGTATAACAT[C/T]GGGCAAAATGTTTTA | 254065 |
rs376981904 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789822 | GACCATGGAACTCCT[-/T]TTTTTTTTTTTTTCC | 254065 |
rs377019073 | snp | C/T | 0.000109514 | 0.00739899 | intron-variant | BRWD3 | GRCh38.p7 | X:80707538 | ATTAAGATATATGGA[C/T]ATTACCAGCTAATGT | 254065 |
rs377076390 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715257 | AAATAAACTAACAAA[A/G]CAATAAAGTTAATTT | 254065 |
rs377084103 | snp | C/T | 0.000119736 | 0.00773652 | intron-variant | BRWD3 | GRCh38.p7 | X:80692172 | AAAAATAAGAAGATG[C/T]AAATCAAATTAATCA | 254065 |
rs377169420 | snp | C/T | 2.32391e-05 | 0.00340866 | intron-variant | BRWD3 | GRCh38.p7 | X:80681949 | CTATATCCTTAATAT[C/T]AGAATTAAACCGAGA | 254065 |
rs377232343 | snp | C/T | 4.58421e-05 | 0.00478737 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80688124 | TCAACAATTTCTGTA[C/T]CCTTAATTAAAAAGG | 254065 |
rs377294896 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795268 | GATAAAGTGAACGTC[C/T]ACATTCTCATCTTGA | 254065 |
rs377299426 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750667 | GAAAATAGTATGGAG[G/T]TTCCTCAAGAAATTG | 254065 |
rs377303760 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779692 | TCTTGAAAGAAGCCA[C/T]GAAAGCGACAAAAAT | 254065 |
rs377305401 | snp | A/G | 3.38432e-05 | 0.00411345 | intron-variant | BRWD3 | GRCh38.p7 | X:80730065 | TTTCTCAAAAATGTA[A/G]ATCACTTTTTTTTGA | 254065 |
rs377308572 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700288 | AAACACAGTCCTTTC[A/C]CTTCAATCAGCTTCA | 254065 |
rs377342561 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731841 | CGGAGCTTGCAGTGA[A/G]CCGAGATCACACCAC | 254065 |
rs377350255 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702929 | ATGTTCCAATGTTAC[A/G]ATAATTTTCATAATA | 254065 |
rs377356916 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768014 | ATTAATGAAATAAAG[C/T]GAAAAGTTTAGAGAA | 254065 |
rs377425620 | snp | C/G/T | 0.000778641 | 0.0197175 | intron-variant | BRWD3 | GRCh38.p7 | X:80809341 | AGGTTCAGAGGGAGG[C/G/T]AGAGAAGAGAAATAG | 254065 |
rs377485315 | snp | C/T | 0.00060965 | 0.0174486 | intron-variant | BRWD3 | GRCh38.p7 | X:80736105 | TTAAAAAAAAAAAAA[C/T]CTGATTCAAATAAAA | 254065 |
rs377524435 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754868 | AAAAAATTAGCCAGA[C/T]GTGGTGGTATGCACC | 254065 |
rs377543287 | snp | C/T | 4.5719e-05 | 0.00478094 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80693039 | TCATCTATTATACTG[C/T]GGAATCTATCACCTA | 254065 |
rs377552275 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804173 | TGGTGCTTTCAGTTT[C/T]AGAGATGAAAATGCG | 254065 |
rs377575329 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753323 | CACCCAGGCTGGAGT[A/G]CAGTGGTGTGATCTC | 254065 |
rs377661265 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803099 | AGCGCAAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 254065 |
rs377719481 | snp | C/T | 2.94338e-05 | 0.00383615 | intron-variant | BRWD3 | GRCh38.p7 | X:80685574 | CTGGTTTCCAGACAA[C/T]TATAACAAAATATCA | 254065 |
rs377725358 | snp | A/G | 6.02192e-05 | 0.00548689 | intron-variant | BRWD3 | GRCh38.p7 | X:80809319 | TCTGGGGAAGAGGGG[A/G]GAAAAGAGGTTCAGA | 254065 |
rs377733385 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708591 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 254065 |
rs377755818 | snp | A/G | 7.36278e-05 | 0.006067 | intron-variant | BRWD3 | GRCh38.p7 | X:80735083 | TTTCACAACTGGATC[A/G]TTAAATATTCTAGAT | 254065 |
rs386825930 | in-del | AG/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727723 | ATCAAGGAGTTGACA[AG/C]TTGAGATTGGGTAAT | 254065 |
rs397697567 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799776 | TCTTTGCAGCATCCC[-/C]AGTTACTACTTATAT | 254065 |
rs397788876 | in-del | -/CAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744300 | GAAGCAGAAATTCAC[-/CAC]AATACCCCCACCCAA | 254065 |
rs397811512 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698721 | TTAAAAAAAAAAAAA[-/A]GAGTAAGAAATCACA | 254065 |
rs397895599 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80719072 | TGTATTTTTTTTTTT[-/T]ATTCAAGAGAAGAGC | 254065 |
rs397895620 | in-del | -/GTGT | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676341 | GTGTTTCGTGTGTGT[-/GTGT]CTGTGTGTGTGTATG | 254065 |
rs397896907 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732579 | ATAAAGGAGAAAGAA[-/A]GTAGGAGAGAGAGAG | 254065 |
rs397897006 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715225 | TTAAAAAAAAAAAAA[-/A]CTTACCAGAGAACAG | 254065 |
rs397897048 | in-del | -/ATAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687120 | TATATATATATATAT[-/ATAT]GGCAGCTGCTATTTT | 254065 |
rs397958897 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793187 | AAAAAAAAAAAAAAA[-/AA]TTACTGATAGGTTGA | 254065 |
rs397962437 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786533 | TATATATATATATAT[-/AT]GGAGTCTTGCTCTGT | 254065 |
rs397975584 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800585 | GTACAAAAAAAAAAA[-/A]CAAGACTGGAAGAAA | 254065 |
rs398087785 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764321 | CAAAGAATTTTTTTT[-/T]TAGAGACGGAGTCTC | 254065 |
rs398087786 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799775 | ATCTTTGCAGCATCC[-/C]CAGTTACTACTTATA | 254065 |
rs527272941 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761441 | ACTGAAGCAATTATA[C/T]GACAGGCAAAGAAGT | 254065 |
rs527348533 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754529 | CCACTCTCGCTAGGA[G/T]TTCCATTACTATGTT | 254065 |
rs527758711 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781953 | AATCTACAGATTCAA[C/T]GCAATCCCGATCAAA | 254065 |
rs528234282 | snp | A/C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80689514 | TAAATGTTGGAAAAT[A/C/G]AAGTGTTGATTTCTC | 254065 |
rs528312083 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751077 | CAGAGTAGAAAGGTA[A/G]TTACCACAGGATACA | 254065 |
rs528660786 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711498 | TGTAAAGCTGTCTTA[A/T]AATCAACATTCTGTA | 254065 |
rs528767453 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688977 | TTTCATAGTCAGACA[A/C]ATTTTCATGAAAAAA | 254065 |
rs529992268 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807125 | ATTAGTAGGCACTGT[C/T]GTTTTTGCCTCTTTT | 254065 |
rs529998150 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80748023 | AATGGGCATCTTTTT[A/T]TTAGAGATGGAGTTT | 254065 |
rs530159723 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716642 | ACGTTGTAGCAGGTA[C/T]CAGAACATCATTCTT | 254065 |
rs531014324 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80686606 | ATGTATTAAATAAAC[A/G]TCTGAAATAAAAGTC | 254065 |
rs531333838 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733596 | AACATCATGAAGTAG[-/T]TTTTTTTTTTTTTAA | 254065 |
rs532166184 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786454 | AATGGTGAAAGATGA[C/T]CTGTTTTCACCCTAT | 254065 |
rs532381812 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80803075 | CCACTGCCTTCCAGC[C/T]TGGGCGACAGCGCAA | 254065 |
rs532445329 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716044 | AGTAGGTTCCCTATA[A/T]GCAGATACCTATTAA | 254065 |
rs532618240 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807753 | TCACTAAAGTATATT[A/C]CATTTTTAAATATGT | 254065 |
rs532622419 | snp | A/G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80706148 | AGTTTCACTCTTGTC[A/G/T]CACAGGCTGGAGTGC | 254065 |
rs532822718 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744576 | TTCTTTCTTTAGGCT[C/T]GACAGCCTTTTTTCT | 254065 |
rs533029584 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768214 | GAGAGCATTCAAATT[C/T]AGGAAATAGAGAGAC | 254065 |
rs533066821 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763905 | GGAAAGACCCTAGAA[G/T]ATAGAAAACAATCTT | 254065 |
rs533333171 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750965 | AACTTGGATGAAATT[A/G]GAAGACATTATGCTA | 254065 |
rs533510896 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80807867 | GGTCTATGCAAATGC[G/T]ACTTAACTGATAATT | 254065 |
rs533793648 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681300 | ATCTGCTATCATAAA[G/T]AAATAAATAATAAAT | 254065 |
rs533906810 | snp | G/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792369 | GCATATTTATACTTG[G/T]GTACATGTTCGTATT | 254065 |
rs534227167 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810848 | TTTCCCGTAACATCC[C/T]GTCCCCACCCCACTC | 254065 |
rs534465265 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | BRWD3 | GRCh38.p7 | X:80725392 | AGAATATGACAAACA[G/T]AATCTTTCAATAACA | 254065 |
rs534633689 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702714 | TAAGATCTCTATAAC[A/T]GGCAATTACAGAAAA | 254065 |
rs534885162 | snp | C/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669375 | TTGGTAATTTCATGA[C/T]TATGAGGATATCATG | 254065 |
rs535386358 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80757771 | GATTTACTGTATATA[G/T]TTTACAAATTTATAA | 254065 |
rs535705288 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765402 | CCCTGTGATTAAGGT[C/G]AATACAAGGCTGGTG | 254065 |
rs535762302 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811394 | AGATATTTCAGCTAT[A/G]GGACCCAAGTCTAAA | 254065 |
rs536205669 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762569 | AGGGTATGTGTTGGG[G/T]GGGTGGGGAAAGGAG | 254065 |
rs536291056 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80788571 | CTTTCACAACAGTTC[A/G]GCAGTTTCTTATAAA | 254065 |
rs536465052 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783386 | TGAGACCCTGTCTAA[-/A]AAAAAAAAAAAAAAA | 254065 |
rs536865406 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698750 | CATGTTTTATTGAAT[A/C]CTCTGATTCTAAAAA | 254065 |
rs536959824 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681684 | AAACTTGTCCAATTG[C/T]TCATCATAAATTTTC | 254065 |
rs537249630 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681766 | GCATCATTTAATCAT[A/G]AAATTTTAAAACTAA | 254065 |
rs537845961 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80743850 | TAGTTATTTATTAAA[A/T]AAGATAATCATATGA | 254065 |
rs538054233 | snp | A/C | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793184 | AAAAAAAAAAAAAAA[A/C]AAATTACTGATAGGT | 254065 |
rs538090711 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799789 | CCCAGTTACTACTTA[C/T]ATGACCTTAGGCAAA | 254065 |
rs538240963 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725865 | GCCTATATAACATAA[C/T]ATGTTTACATGTGTT | 254065 |
rs538279665 | snp | A/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811173 | GACAAAACAAATATG[A/T]ATAATTGATACAACA | 254065 |
rs538290414 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729612 | AGGTAGAAAGTAAAA[C/T]AGATATATTTTTTAA | 254065 |
rs538468242 | snp | A/G | 0.00317376 | 0.039709 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810349 | AGTCGCTATTTGGTC[A/G]TGACTTGTTTCTGTT | 254065 |
rs538475656 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695716 | AGGTATTTGCAGAAG[G/T]TTTAGAGATTATAAG | 254065 |
rs538552163 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80793960 | GAGGCAGGTACATCA[C/G]TTGAGGTCAGAAATT | 254065 |
rs538668411 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726030 | TGTCTATATAACATA[-/TA]ACATGTTTACATGTT | 254065 |
rs538786513 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676361 | TGTGTGTGTGTATGT[A/G]TGTGTATGTGTTTGT | 254065 |
rs538854931 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685702 | CATTCTCCTTTGCTA[C/T]GAAAAACACAAGACT | 254065 |
rs538944749 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80757075 | TGTATTCACTATAAT[A/G]GCATCATTACATTCT | 254065 |
rs539015968 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80696578 | CAAATATAAATAAAA[C/T]GGAGAAATAAACTAG | 254065 |
rs539269087 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783443 | CTGGTGAGGTTTTGG[A/G]GAAAAGGGAACCCTT | 254065 |
rs540645387 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80683524 | TGATTAAAAGCTAAT[C/G]AGATACCAGTGATTT | 254065 |
rs540824551 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80737241 | TAGATGCTCAAGTCC[C/T]TGATATAAAATGGTA | 254065 |
rs540861177 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766130 | CTCCCCAATGAATCC[A/G]GTGGGCTTTATTCAA | 254065 |
rs540936730 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713886 | GCCTTACAAACCATA[C/G]AGTCCCATCAGAGCG | 254065 |
rs541060809 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758569 | CAGCTGCTCTAATTA[A/G]GGGAGACTCTACCTT | 254065 |
rs541814085 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80776995 | TTGGGAGTTTACTCG[C/T]TCACTATACATAAAT | 254065 |
rs541849228 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795492 | ATCTATACATGTATG[C/T]GTATATATGTATATG | 254065 |
rs542195139 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748053 | TCAACATGTTAGTCA[C/T]GCTGGTCTTGAACTC | 254065 |
rs542288395 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80794855 | TCATTCAGTAGTGAC[A/G]AACTGATCCAAAATC | 254065 |
rs542759445 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735509 | TTTCTATATAAATTG[C/T]CTCTTCAACATTAAT | 254065 |
rs543271635 | snp | C/T | 0.00709118 | 0.0591211 | intron-variant | BRWD3 | GRCh38.p7 | X:80707551 | GATATTACCAGCTAA[C/T]GTATTTCTAATTAAA | 254065 |
rs543533584 | snp | A/C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766671 | AATAGGAACAGCTCC[A/C/G]GTCTGCAGCTCCCAG | 254065 |
rs543571017 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759056 | TAAGAGCACAATGTT[C/T]CAGTGGTCTTATCAG | 254065 |
rs544553725 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80745259 | TAACAAACATTTAAT[A/G]AATGTTTGTTAAAAC | 254065 |
rs544636991 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710658 | AAGGCAAAGCCTGCT[C/T]AACCTGCTGATTAAC | 254065 |
rs544727071 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701359 | TCGAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 254065 |
rs544816184 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684752 | GGAAAGATTTCATTT[C/T]AACCTAAATCCAGTA | 254065 |
rs544901699 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | BRWD3 | GRCh38.p7 | X:80772345 | CAGTTGGAAACCATC[A/G]TTCTGAGCAAACTAT | 254065 |
rs544940807 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80704053 | GGGGAAAAGAAACTG[C/T]CATTGGGATGAAATA | 254065 |
rs545281823 | in-del | -/GA | 0.332636 | 0.235948 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809700 | GAGGAGAGGGAGAGG[-/GA]GAGAGAGAGAGTGAG | 254065 |
rs545626479 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728925 | ACAAAACAATTTGCA[A/G]TATTCATATCTTATA | 254065 |
rs546287574 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80801068 | AGTCCAACAAAAGAA[A/C]CCAGTACCAACTAGC | 254065 |
rs546758787 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80751756 | CACTGTCTACCATTC[C/T]ACTCTCTACATCCAG | 254065 |
rs546982891 | snp | A/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675230 | CTATAAAATAATGAT[A/T]CACAACATGAGTGTG | 254065 |
rs547293665 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80689417 | TTTAATATTTTCTAT[A/G]CAGCATATAGAAAAT | 254065 |
rs547465346 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762649 | CAGATGAATAGCTCA[A/C]TTAAGCACTGGCAGA | 254065 |
rs547502059 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755619 | GCACATCTATTACTC[C/T]ACCTCTGGGCATCTA | 254065 |
rs548189202 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790229 | AAAAAGATATACCTT[C/T]ATGATTAAATTTTGT | 254065 |
rs548245142 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721900 | CGCCCAGTCTGGAGT[A/G]CAGTGGCGCAATCTT | 254065 |
rs548281471 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749600 | ATGAGTCTCCTGTAG[A/G]CAGCATATTATTGGG | 254065 |
rs548450116 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721060 | TTTTTGAAAGAAGTC[A/G]AAATGATGATCTTTC | 254065 |
rs548472804 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80807308 | ATTTTCTGTGATTTG[C/T]AAAATATAAGAAAAC | 254065 |
rs549062323 | in-del | -/ATAACATGTTTACATGTGTTACATGCCTATATAAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725791 | ATGCCTATATAACGT[lengthTooLong]ATAACATGTTTACAT | 254065 |
rs549558015 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688478 | AAAATTATTAATTAT[A/T]CATGATTACTCCATT | 254065 |
rs550076177 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80743768 | GGCATTTACAGGTTT[C/T]CTCCCTTCTTAACAA | 254065 |
rs550491837 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804399 | TGAGCTACCACACCC[A/G]GCTAATGTTTGTATT | 254065 |
rs550844589 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697108 | TCAAATTTAATGATC[C/T]GAAATCCTACACCTA | 254065 |
rs550854287 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786819 | CCAGCCTAATCCACC[A/G]TGCCCGGCCTAATCC | 254065 |
rs550940327 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716411 | AGAAAGTTGTGCAAC[C/T]ATTACCAGCATTTCC | 254065 |
rs551123213 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80690764 | GTAGCACCTTAATAA[C/T]GATGAATCCACAAAC | 254065 |
rs552299248 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80808432 | CTTTGGCTCTGCACC[A/G]AGCTCTAGAACCTCG | 254065 |
rs552361363 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80783888 | AAACAATTAAACTCA[C/T]GGAAATAGCAGAATG | 254065 |
rs552560739 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801900 | CAATCAGAAGGGTTG[A/C]GAATCCCTGCAATAA | 254065 |
rs552650221 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80719204 | AAGGGCTAGACTTAC[C/T]GTAGCACTTCACTTC | 254065 |
rs552836746 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703068 | AACTACATTCCCCTG[C/T]TCATTTAAAGGAGTA | 254065 |
rs552898174 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80727401 | CCCTGTCCACTTTTC[C/T]AATTGTATCTGGGGA | 254065 |
rs553179559 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712722 | CGCCTCTTCCCGGCC[G/T]CCCATCGTCTGAGAT | 254065 |
rs553501091 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672107 | GTCTCACATTCTAGA[A/T]TTAATTTAGAAGAAA | 254065 |
rs553537814 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774197 | TCGCATATATATTTT[C/T]GTTCTATCCTGACCC | 254065 |
rs553751126 | snp | C/T | 9.12461e-05 | 0.00675387 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682506 | ACTGCTGCTGCTTCT[C/T]AGACGTTTTCTGTAC | 254065 |
rs554615479 | in-del | -/AAATAAATAAATAAAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788090 | CTCTGTCTCAAAAAT[-/AAATAAATAAATAAAT]AAATAAATAAATAAA | 254065 |
rs554663789 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80736684 | ATCATTGTGGGAAAA[C/T]GGAGATCAAGTTAAA | 254065 |
rs554749832 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763717 | AAATTACAAAATGGT[A/G]AAGAAAAAAAATCAA | 254065 |
rs555112419 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80701316 | ACTTTGGGAGGCCGA[C/G]ATTGGTGGATCACCT | 254065 |
rs555247648 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80682259 | AGTGAAACTTCAATC[A/G]TTAAAATTTAAAAAA | 254065 |
rs555357936 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765667 | TCCTTTATCATGTAA[A/C]ATAAGATGTACTAAC | 254065 |
rs556318039 | snp | C/G | 0.00475684 | 0.0485365 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810356 | ATTTGGTCGTGACTT[C/G]TTTCTGTTTAAAATT | 254065 |
rs556481092 | snp | G/T | 0.00010119 | 0.00711231 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793767 | AATGTGTGCATTTGC[G/T]GCCACCTAAAAAAGT | 254065 |
rs556895247 | snp | C/T | 2.32737e-05 | 0.0034112 | intron-variant | BRWD3 | GRCh38.p7 | X:80733432 | TCAAACATTTGTTTA[C/T]ACAAATATGTATTAC | 254065 |
rs556920008 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784167 | TACACATTGTATCCC[C/T]GTACAAAATATCTCA | 254065 |
rs556941307 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758187 | CAGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 254065 |
rs557155432 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773824 | CATCTCTCCTTCTTG[C/T]AATGCCCATTACACT | 254065 |
rs557188226 | snp | C/G | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717678 | TTGTTATGCATTTGT[C/G]TAACACCTTCAATTT | 254065 |
rs557413475 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680543 | TTGTGATATAGCAGG[C/T]CCCTAAGGAAGAGGA | 254065 |
rs558207512 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811486 | TATTTTCAATAACTT[C/T]GTGCACGAAACAAAG | 254065 |
rs558330877 | snp | G/T | 0.00738971 | 0.0603345 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792920 | TGTAATCCCAGCACT[G/T]TGGGAGGCTGAGGCA | 254065 |
rs558904504 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804245 | AACTTTGGTTCAGTC[-/T]TTTTTTTTTTTTTTG | 254065 |
rs558948838 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80683902 | TGCTAAATGTATCTT[C/T]ATGCATGCCTAACAA | 254065 |
rs559082194 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767687 | CTCCAAAGGATTGCA[A/G]CTCCTCGCCAGCAAC | 254065 |
rs559235193 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685773 | GTTGAACACAATCTC[A/G]TTCCTTACTTGAATG | 254065 |
rs560135830 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80796470 | GGAGAAAAAATCTCA[A/G]ATTCTCGTATCAGGA | 254065 |
rs560249390 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778011 | CAATTTTTCAATAAA[C/T]GGCATTGAAAGAGAA | 254065 |
rs560341387 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696523 | ATAACATAAATACAC[-/AC]ACACACACACACACA | 254065 |
rs561145960 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715505 | ATTTGGTGTACCTGA[A/G]AGTATTCTGCTTAGC | 254065 |
rs561487806 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711127 | GTGTATATATAATGT[A/G]TGTTTATTTAGTTCT | 254065 |
rs561583426 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80688621 | AGACCCAAGCACCAC[C/T]AGTGCTGGTGAAACA | 254065 |
rs562206774 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739636 | TCATTATTTAGTAGA[C/T]CCTCCTTATCTGCAG | 254065 |
rs562803188 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806013 | GCCACTCAAAATCAG[G/T]TCATATGTGAAATAA | 254065 |
rs562919886 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80746949 | TATAAACAATTAGAA[C/T]ACATAAGAGACCTGA | 254065 |
rs562995782 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773411 | GCATAGGCTAAAATT[G/T]CATGCTTTTTCATGA | 254065 |
rs563232565 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776350 | CAACTATTTCACACA[A/G]GCATGAAACTTCAAA | 254065 |
rs563246795 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705559 | AGAAATGCATCATTA[A/G]GTGATTTTGTCATTG | 254065 |
rs563392307 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80686019 | AAGTCCCTACAAAGG[A/G]CATGAACTCATAATT | 254065 |
rs563543942 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759084 | CAGCACAGAGTACAG[C/T]GTATTATTTTCCTTC | 254065 |
rs564033806 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80775456 | TTACCAATTCCTATC[A/G]TATTATCTCATGTCT | 254065 |
rs564342415 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740969 | CAACATGCAGGTTTG[C/T]TACATACGTATACAT | 254065 |
rs564376969 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80802119 | TATTCTTTTTTTATA[A/G]TACTGTTTTATATGC | 254065 |
rs565104042 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784792 | TGCCTATCATTGATG[A/G]GCATTTGGGTTGGTT | 254065 |
rs565478969 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739398 | ATGTGATGATGCCAA[A/G]AAGATAGTTGCATAA | 254065 |
rs565524714 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715123 | CTAAGTACCCTGTCC[A/G]TTAGTCTCAGCCAAG | 254065 |
rs565895344 | in-del | -/AA | 0.188741 | 0.242378 | intron-variant | BRWD3 | GRCh38.p7 | X:80777072 | TGATTATGCTTAAAC[-/AA]AAAAAAAAAAAATGC | 254065 |
rs566486507 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80807593 | CTACCCTCCAATGCA[C/T]TGTGGCAGCAGCTAA | 254065 |
rs566597224 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80791372 | TACTAGTATTTCTTC[A/G]TAATGGTCTGGCCAG | 254065 |
rs566624098 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749886 | ATGATACTGACGTAG[A/G]AACAGACACATCAAC | 254065 |
rs567134944 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724407 | GTATTTCCATCATCA[C/T]AGAATGGTGGATATG | 254065 |
rs567373184 | in-del | -/AATTG | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80730809 | TTTTCTACTACAAAA[-/AATTG]AATTGAACTACATAT | 254065 |
rs567669549 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790868 | GGCAAAGTGAACACT[A/G]GAAAATTCTGGTGGA | 254065 |
rs567910666 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669738 | TTCTAACTAGAATTG[A/C]AACATGACAAAAATC | 254065 |
rs567938743 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712603 | GAGCGTCTCTGCCTG[G/T]CTGCCCATCGTCTGG | 254065 |
rs567988180 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754335 | TACAGAAATGCTACT[A/G]ATTTTTGTACTTTGA | 254065 |
rs568623199 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80708166 | TTTGGAAGGCCAAGG[C/T]AGGCAGATCACCTGA | 254065 |
rs568661738 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80721419 | TGTGTAATACCATTT[C/T]CCTGCTCTACAACCT | 254065 |
rs568878413 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762070 | AAAAATGCAAGAGAC[A/C]AAAAAATACAGCTGA | 254065 |
rs569168640 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786969 | AAAGAATCCCAAAGA[A/G]TCTCAAGGGAAAAAA | 254065 |
rs569283681 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716430 | ACCAGCATTTCCAAA[A/G]CTTTTTCATCACTTC | 254065 |
rs569290177 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697628 | TGGCCTCCAGCTCCA[C/T]CTATGCTGTTGTAAA | 254065 |
rs569526114 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793912 | GCCTGGGCGCGATGG[C/T]TCACGCCTGTAATCC | 254065 |
rs569635681 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706482 | TTTTTTTATTTTAAA[-/AT]TTTGTTTAAAAACTA | 254065 |
rs570446997 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80809360 | GAAGAGAAATAGAAG[C/G]TTTTTCAAAAGAAAC | 254065 |
rs570591314 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755627 | ATTACTCCACCTCTG[A/G]GCATCTATCCTGGGG | 254065 |
rs571194692 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735803 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 254065 |
rs571478982 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753714 | TATGGTTAGAGATAC[A/G]GGTCCAGTTTTATTC | 254065 |
rs571510843 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728440 | CTCTACCCCTATAAC[A/G]GTAACAATGAAAAAA | 254065 |
rs571587667 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693744 | AAGGATTCAAGGGGT[A/G]ACTTGGCTGCTGTTA | 254065 |
rs571792034 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675387 | GTTAAATTTTAAGAT[C/T]CAAATGAAAACCAGC | 254065 |
rs572074248 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80799410 | AGTAACTCTAAAAAA[C/G]AAATATAGCAGAGAA | 254065 |
rs572814435 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710443 | TTGGAGAGACATATG[C/T]CTAAATTTATGGAAT | 254065 |
rs572962527 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763937 | ACAAAACTAAAGTGA[A/G]AGGGAGTCTTCTTCC | 254065 |
rs573476519 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702353 | GAATGGAGAAAAATA[G/T]TCCTTAGACAGGAGT | 254065 |
rs573476869 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736973 | AAGGATTAAGATATA[C/T]AGGGTTTGAATACAT | 254065 |
rs573541881 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687413 | ATCCTTTGTGGTCAT[G/T]ATAAATTCTGTTGTG | 254065 |
rs573561276 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80682366 | CAAACAAAAAAAGAC[A/C]TCTTGGGATCTCCCC | 254065 |
rs573617448 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767682 | TTCTCCTCCAAAGGA[C/T]TGCAGCTCCTCGCCA | 254065 |
rs573626749 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785745 | GGAAACTTAAAAATC[A/T]GGCCAGGCGCAGTAG | 254065 |
rs574496274 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736870 | GACACAGGAAAAAGC[A/T]GAAAATTGGACAAGA | 254065 |
rs574541618 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775737 | TGCATATGAGCTACA[C/T]AGTCTTTTCATAAAG | 254065 |
rs574664509 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810975 | CTATATTCTTGGGAA[C/T]TGGGTTTCCTCACTC | 254065 |
rs574682044 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805189 | TTCTAGAATATGTAA[C/T]TTAGTATAAACACTG | 254065 |
rs574777036 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793927 | CTCACGCCTGTAATC[C/T]CAAAACTTTGGGAGG | 254065 |
rs575103247 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734793 | TCAATATGGAGCAAC[A/G]GTACATGTTTTTTTG | 254065 |
rs575264833 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707375 | TACGAGAACATAATT[C/T]CGTATTAAAACTGTT | 254065 |
rs576054371 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783996 | AGATACAATGAGTAA[G/T]ATCTAGTATTTGATA | 254065 |
rs576199968 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | BRWD3 | GRCh38.p7 | X:80680616 | AAGCGGTTATTGACT[A/G]AAAGAAGGCTCATTT | 254065 |
rs576458274 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704795 | TCTTTTTGGGGGTTG[C/T]AAATTTATTCCAGCA | 254065 |
rs577129692 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80745400 | ACATTTTTGTTCATT[C/T]GTTTACTTATATAAA | 254065 |
rs577165543 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737376 | TTGTTATACTATATT[A/G]CTTAAGGGATAATGA | 254065 |
rs577335421 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80770234 | GAAAAAGAGGGAAAC[C/T]TCCCCAACTCATTTT | 254065 |
rs577374589 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792944 | TGAGGCAGGCGGATC[A/G]CGAGGTCAAGAGATC | 254065 |
rs577549344 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80684557 | CAAATTAGGCACATA[A/T]TTCCACGATTCCTTG | 254065 |
rs577612190 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703839 | GACTACCTGAAAACC[A/G]TAACTTTTACATACG | 254065 |
rs577695287 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80775567 | TGTATTGTAAAGATT[G/T]CAGAACACTTAAAAT | 254065 |
rs730882185 | snp | G/T | | | splice-donor-variant | BRWD3 | GRCh38.p7 | X:80692088 | CAATTCCAGAAGGAA[G/T]TAAATATGCTTTTAA | 254065 |
rs730882186 | in-del | -/A | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735165 | TTACTGAGAGATCCA[-/A]GACCTGGAGTCCAGA | 254065 |
rs745309747 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770329 | ACCAATATCCCTGAT[A/G]AACATCGAAGTGAAA | 254065 |
rs745316368 | snp | C/T | 2.38104e-05 | 0.00345031 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80684144 | AGTCCACAGGAGTAT[C/T]TATAACATCTTGATA | 254065 |
rs745327363 | in-del | -/TC | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674089 | GCAAACAGAAAATTA[-/TC]TGTTTGTTTAATAAA | 254065 |
rs745336278 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696278 | CTTTAATCTCCTTAC[A/G]TTTTAAACTCAACTT | 254065 |
rs745346681 | in-del | -/ACTA | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674138 | TAACATACCCTGATG[-/ACTA]ACTCTTTAAATCTTA | 254065 |
rs745377892 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698333 | GCTAGAATTGAAATC[C/T]AGGTCTTATTCCAAA | 254065 |
rs745381405 | snp | A/G | 6.4319e-05 | 0.00567057 | intron-variant | BRWD3 | GRCh38.p7 | X:80809045 | CCTGCACTAGCACCT[A/G]AGCAAAAGGGAAACA | 254065 |
rs745401261 | snp | A/G | 2.41473e-05 | 0.00347463 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80696809 | GCTTCAAGCAGCACA[A/G]TGTGGGTGGGCCAAC | 254065 |
rs745411124 | snp | A/G | 7.27987e-05 | 0.00603275 | intron-variant | BRWD3 | GRCh38.p7 | X:80682661 | ATATAGTCTTAACTA[A/G]TTTTATATTTTAAAA | 254065 |
rs745428884 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754201 | ATTTCCTAAGTGTTC[C/T]GTAGTTTTCTATGTA | 254065 |
rs745436394 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80710767 | GCTGGAAGACATACT[A/G]ATGATACTAATCATC | 254065 |
rs745460017 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782617 | AATAACCAGAATATA[C/G]CCAGGCACAGTGACT | 254065 |
rs745467399 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689098 | CAATCTAGCATATGT[C/G]AGTCACTCATCCCTG | 254065 |
rs745482341 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751508 | CAAATATTTGAGTTC[C/T]TTAATGGCCAAAGAA | 254065 |
rs745498846 | in-del | -/A/AAAA/AAAGAAAC/AAAGAAAGAAAGA/AAAGAAAGAAAT | 0.00370314 | 0.0428947 | intron-variant | BRWD3 | GRCh38.p7 | X:80730425 | AAGAAAGAAAGAAAG[lengthTooLong]AAAGAAAGAAAGAAA | 254065 |
rs745499292 | in-del | -/AA | 3.36264e-05 | 0.00410026 | intron-variant | BRWD3 | GRCh38.p7 | X:80736117 | AAATCTGATTCAAAT[-/AA]AAAGTTTTCATGTTC | 254065 |
rs745504545 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721413 | AGCACATGTGTAATA[C/T]CATTTCCCTGCTCTA | 254065 |
rs745519485 | in-del | -/AGT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729671 | GGCTCTGTAGGCATC[-/AGT]AGAACACAGAGATCT | 254065 |
rs745554627 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711417 | CATAACATCATACAA[C/T]AGAGAAAGAAGGAAA | 254065 |
rs745555544 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80752906 | CTGACCTCAGGTGAT[C/T]CACCAGCCTCAGCCT | 254065 |
rs745565131 | in-del | -/CGCGGGGGGTGGGGGGGCG | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809805 | AGAGAGAGAGAGAGA[-/CGCGGGGGGTGGGGGGGCG]GAGAGAGAGAGAGAG | 254065 |
rs745569682 | in-del | -/AC | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80761167 | AATCAAGAAATTATT[-/AC]AGAGTGGTTATACTA | 254065 |
rs745572809 | snp | A/G | 9.63913e-05 | 0.00694164 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80730011 | TCGACTTCCACTAAC[A/G]AATCTTAAACTAGAA | 254065 |
rs745616086 | snp | C/T | 2.33981e-05 | 0.00342031 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677258 | TTCTCTTTATCTTCT[C/T]CTCCCATGTTTTCAT | 254065 |
rs745616197 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741993 | CCTTGCCCATGCCTA[C/T]GTCCTGAATGGTATT | 254065 |
rs745624208 | in-del | -/CTGT | 2.29996e-05 | 0.00339106 | frameshift-variant, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709438 | ATAACCTCTGAAGAA[-/CTGT]CTGAGTCTTCCTGTA | 254065 |
rs745643298 | snp | C/T | 2.29822e-05 | 0.00338977 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717736 | TTGGGGAAGAAGATA[C/T]GTCCATGTTTGGACT | 254065 |
rs745651059 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772400 | GCATGTTCTCACTCA[C/T]AGGTGGGAATTGAAC | 254065 |
rs745655576 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80736026 | CCATTGCCAGAAACA[A/G]ATTGTTCCATCAGCA | 254065 |
rs745657741 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80797867 | TTGGGAGGCCGAGGC[A/G]GATGGATCACAGGGT | 254065 |
rs745660507 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711891 | TCTAAATTGTATAAA[C/T]CCAACCAGTAGCCTG | 254065 |
rs745662093 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773083 | GGGGTAGGGGAGTCA[C/T]GCAGGAGGGAAGCCG | 254065 |
rs745665225 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783712 | CAAAGAAAATGTGGT[A/G]TTTATACGCAATGGA | 254065 |
rs745695173 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80724257 | TCCTAAAATTAAAGC[A/G]CACAATCAATTTTAC | 254065 |
rs745721873 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808463 | TCGGCTGAGAGGTGG[C/G]GGGCGGGTTGGGGGT | 254065 |
rs745755470 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80798475 | TATTATAAACCACTC[C/T]TTTTGTTTAAAGCTC | 254065 |
rs745755977 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80707253 | AAAGGCCCACAGTGA[C/T]GTCAGAAAGGTATTG | 254065 |
rs745766953 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731287 | GGACATCTCCTCATG[C/T]GTTTATTGGCCACAC | 254065 |
rs745768655 | in-del | -/AT | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80726220 | ATATGTCTGTATAAC[-/AT]ATAACACGTTTACAT | 254065 |
rs745770715 | snp | A/G | 2.29247e-05 | 0.00338553 | intron-variant | BRWD3 | GRCh38.p7 | X:80681326 | TAAATGTCTTGTCCT[A/G]TATTTATTTCCTACC | 254065 |
rs745770842 | snp | C/G | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669274 | TTCAACTACTGTTTT[C/G]TTTTAGTAACTTCTT | 254065 |
rs745774288 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80788169 | AGGGCCAGGGACAGT[A/G]GCTCATGCTTGTAAT | 254065 |
rs745781642 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735321 | AACAAAAGGAACGTG[G/T]TCAATAAGTACTATT | 254065 |
rs745788502 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756020 | ATTTTTATCTTAAAC[A/G]TACATTTTCTATTAG | 254065 |
rs745794876 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726318 | ATGTTATGTCTGTAT[A/G]ACATATAACATGTTT | 254065 |
rs745838089 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766723 | GTGATTTCTGCATTT[C/T]CAACAGAGGTAGCTG | 254065 |
rs745843825 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714721 | AAATCTCTTCAAATA[A/T]TTTAAAATTTGATTC | 254065 |
rs745848612 | snp | G/T | 2.43208e-05 | 0.00348709 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695951 | ATTATAAAACTGATG[G/T]AGCACAAGGAAGTCA | 254065 |
rs745849020 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675127 | TTTGGGGAGTAAAAC[C/T]GACCTTGGAACTCAA | 254065 |
rs745865727 | snp | C/T | 2.29103e-05 | 0.00338447 | intron-variant | BRWD3 | GRCh38.p7 | X:80688038 | GGAAACCTGAAAACA[C/T]ATCTCCTCAGCAGTT | 254065 |
rs745866354 | snp | A/G | 2.28449e-05 | 0.00337963 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719549 | CTCCTTCATTAATTA[A/G]TCTCAGGTCTTGTTC | 254065 |
rs745869589 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80742866 | TTTGACTTCCTCTTT[C/T]CCTAATTGAATACCC | 254065 |
rs745871272 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734677 | GCTAAAATGATAAAA[C/T]TTTAGGTTCTGTATA | 254065 |
rs745883069 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80740041 | TGAGATCACAAGTAA[C/G]TGATAATCTCCCAAA | 254065 |
rs745892823 | snp | C/T | 2.2905e-05 | 0.00338408 | missense, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704760 | CTGCTGCATATTTTA[C/T]GTGTTGTCTGTCTGG | 254065 |
rs745901914 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80677726 | AGAAGCTTTGAATAC[A/G]GCAATGAAAGGGACA | 254065 |
rs745921042 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770871 | CTGTCTCAGCCCAAA[A/G]TCTCCTGAAGCTGAT | 254065 |
rs745939473 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780639 | TTACTTGCAGGTGTG[A/T]CAAGAATCTCTTGAT | 254065 |
rs745956867 | snp | C/T | 6.92233e-05 | 0.00588276 | intron-variant | BRWD3 | GRCh38.p7 | X:80703637 | GTATAAAACACAGTT[C/T]TCCAATACATAAAAC | 254065 |
rs745957626 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80781464 | TAGGGATTCTTAGTC[A/G]GCCTGGGAAATCCAG | 254065 |
rs745960742 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758791 | TCCCATCTTTAAAAA[A/C]TAAACTAAAAAGAAA | 254065 |
rs745962293 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749295 | CCTATTATTGTATTG[C/T]AGTTGCAGTGTCTCT | 254065 |
rs745977084 | snp | A/G | 2.36393e-05 | 0.00343789 | intron-variant | BRWD3 | GRCh38.p7 | X:80725075 | TCATGTCCCTATAAT[A/G]AAAATCAGTATTAAC | 254065 |
rs746003057 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708063 | ATTAGGATTTGTTTT[-/A]AAAGTACAACCGCAA | 254065 |
rs746013626 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687156 | TTTCTTAGTTTAAAT[C/T]AGACAGTATTTTCCC | 254065 |
rs746022286 | snp | A/G | 0.000405289 | 0.0142296 | intron-variant | BRWD3 | GRCh38.p7 | X:80703611 | AAAACATAAATACAC[A/G]AAAAGTATATGTATA | 254065 |
rs746031564 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783386 | GTGAGACCCTGTCTA[-/A]AAAAAAAAAAAAAAA | 254065 |
rs746031646 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | BRWD3 | GRCh38.p7 | X:80713434 | GCTGTGTCCACTCAG[A/G]GTTAAATGGATTAAG | 254065 |
rs746056253 | snp | C/T | 6.85902e-05 | 0.0058558 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676963 | TCCTCTTCCTCTGCC[C/T]CCTCTACTCCATCTA | 254065 |
rs746057761 | snp | C/T | 2.33694e-05 | 0.00341821 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735188 | CTCAGTAAATTTCAC[C/T]GGGCGATCTCTAAAG | 254065 |
rs746060586 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678573 | TCAGTAAAGAGATAA[C/T]ATTTAGGGTAATGAG | 254065 |
rs746102641 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80712929 | AGCCGCCCCGTCTGA[G/T]AAGTGAGGAGCTCCT | 254065 |
rs746126472 | in-del | -/AAC | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80763618 | GAAACCAAAATTAAA[-/AAC]AAAATCTATTTACGA | 254065 |
rs746128182 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722274 | TACAACTCCATACTA[C/T]AGAAAACAACAGCTT | 254065 |
rs746155650 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740820 | ACATTAACCTAAACA[A/C]AGACACACACATACT | 254065 |
rs746172159 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776647 | AATTAACAGGAAACA[C/T]TGTTTTTCCTAAGGT | 254065 |
rs746177558 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754517 | TCTCTCATCTGACCA[A/C]TCTCGCTAGGATTTC | 254065 |
rs746189305 | snp | A/C | 4.57488e-05 | 0.0047825 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682009 | TACCAGGAGATGAGA[A/C]AGGAGAGCTAGTCCT | 254065 |
rs746201730 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80725960 | CATGTCTATATAACA[C/T]ATAACATGTTTACAT | 254065 |
rs746229743 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776077 | TGTTGTCTATTTAAT[A/G]ACATTTTACAAAATG | 254065 |
rs746252018 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745574 | TTACACTCACTGTAA[A/G]AATTCTTCTCCCGCT | 254065 |
rs746262360 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678892 | ATTAGGGCATTTAGG[G/T]AGGTAATTAAGGTTA | 254065 |
rs746265253 | snp | A/G | 4.36405e-05 | 0.00467101 | intron-variant | BRWD3 | GRCh38.p7 | X:80691997 | GGTATAAGATAAAAA[A/G]AAAAAAATTAGAAAA | 254065 |
rs746292315 | in-del | -/TACAA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773734 | CTCCATTTCTCAAGT[-/TACAA]TGAACCCTTCAAAGT | 254065 |
rs746310463 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800851 | AAATGCTAATCATTA[C/T]GCATAGCATTTCTTT | 254065 |
rs746327219 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737363 | CTGTAGTAATTTGTT[A/G]TTATACTATATTACT | 254065 |
rs746327941 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80695268 | TGATTTTTTCTTTAT[A/G]AATTACCCAGTCTCA | 254065 |
rs746339479 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684314 | CCCCAAAACATCTTT[C/T]GGTGGCTCATAAAAA | 254065 |
rs746352783 | in-del | -/ACAAA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745809 | AAATATTAAGATGAG[-/ACAAA]ACAGAGTACATATAT | 254065 |
rs746356101 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726670 | TGCTATTAAAAAAAA[C/T]AGAATAGAGTATCCT | 254065 |
rs746372008 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80718332 | TTTACAAATAAAACA[C/T]AAATGGAAACTGAAA | 254065 |
rs746390245 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80717150 | AATCCTAATGAAATT[A/C]TTTCACCCAATGAAG | 254065 |
rs746403224 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774401 | AAGTTTCTGGGACTA[C/T]AGGTGTGTGCCACCA | 254065 |
rs746408850 | snp | A/C | | | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704304 | ATTTATCATACTCTT[A/C]CATGTTACAAGTTAA | 254065 |
rs746415817 | snp | A/G | 2.43894e-05 | 0.003492 | intron-variant | BRWD3 | GRCh38.p7 | X:80723909 | CTCAAGTCATCTTAA[A/G]AGTAATTTTCAAATA | 254065 |
rs746417037 | in-del | -/A | 0.00317628 | 0.0397247 | intron-variant | BRWD3 | GRCh38.p7 | X:80745122 | ACCAGTACTGAAACC[-/A]AAAAAAAAGATATAA | 254065 |
rs746426026 | in-del | -/C/CC | 0.0423074 | 0.139541 | intron-variant | BRWD3 | GRCh38.p7 | X:80777143 | AAAGCACTCTTAAGA[-/C/CC]CCCCCCCCCACGAAA | 254065 |
rs746433394 | snp | C/T | 2.41458e-05 | 0.00347453 | intron-variant | BRWD3 | GRCh38.p7 | X:80682135 | AGCATTTTTTTTTTT[C/T]TGTTAGCAACATATT | 254065 |
rs746435523 | snp | A/C | 2.61042e-05 | 0.00361268 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695909 | AATTCTATATTTACC[A/C]ATCTGCCAGTTCCTT | 254065 |
rs746448083 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786937 | TCTTTATTTGCAGAC[A/C]ACAGGGTTATCTATA | 254065 |
rs746453992 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740656 | CAGGAGGTGGAGGTG[G/T]GAAGATCACTTGAAC | 254065 |
rs746471019 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744997 | CCACACTTCTATGTT[A/C]ATACTAAAGCAATGA | 254065 |
rs746484537 | snp | A/C | 0.00707956 | 0.0590733 | intron-variant | BRWD3 | GRCh38.p7 | X:80777072 | TTGATTATGCTTAAA[A/C]AAAAAAAAAAAATGC | 254065 |
rs746496356 | snp | A/G | 0.00426324 | 0.0459722 | intron-variant | BRWD3 | GRCh38.p7 | X:80800760 | GCAGGGGAAAAAAAA[A/G]AAAAAAAAGACAGCA | 254065 |
rs746503290 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80682687 | TAAAAAAAGGTATAA[A/T]CATGCCTAGACCAAT | 254065 |
rs746514246 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80768097 | AAAAGACCAAATCTA[C/T]GTCTGATTAGTGTAC | 254065 |
rs746525226 | in-del | -/T | 2.94014e-05 | 0.00383404 | intron-variant | BRWD3 | GRCh38.p7 | X:80707552 | TATTACCAGCTAATG[-/T]TATTTCTAATTAAAA | 254065 |
rs746526931 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721150 | CACTGAAACTTAATG[A/T]TTATTTCTGAATGAA | 254065 |
rs746536339 | snp | G/T | 2.28428e-05 | 0.00337948 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717709 | GACTACTATGTCTTC[G/T]AAGCCTGATGTTTGG | 254065 |
rs746548990 | snp | C/T | 2.46424e-05 | 0.00351007 | intron-variant | BRWD3 | GRCh38.p7 | X:80692198 | AATCATATAGTACTT[C/T]CTTTCATATACTACC | 254065 |
rs746563747 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716986 | GCTTGGTTAGGAAGA[C/T]ACTTGATTAAAATGA | 254065 |
rs746570436 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768775 | GCCCTAATTGAAAGA[C/T]ACAGACTGGCAAATT | 254065 |
rs746588377 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810476 | TCTGACAAATATTGC[A/G]TGAGAAATTTGCAAT | 254065 |
rs746598090 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789177 | ACATCTGACCATGAA[C/T]ATGACAGATAGTCTA | 254065 |
rs746598237 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80693973 | CCAAGAAAATGGGGG[A/G]AAATGTCTTCCAGGG | 254065 |
rs746630011 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728596 | AGCGCGTGTCATCCC[C/T]ATTTTACAGATATGT | 254065 |
rs746647525 | in-del | -/AGCTTTATGG | 2.45963e-05 | 0.00350679 | intron-variant | BRWD3 | GRCh38.p7 | X:80691191 | CAAAATTATGAAAAT[-/AGCTTTATGG]CAAATAAGGTAGCTA | 254065 |
rs746650543 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680562 | TAAGGAAGAGGATAT[C/G]TGACTTACATAACTG | 254065 |
rs746658695 | in-del | -/CAAATATTC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732188 | CTCAGTATACATATG[-/CAAATATTC]CAAAATCTGTAAAAA | 254065 |
rs746671341 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809582 | GAGTCCCGCCGCTTC[C/G]GCCGCACTCCTCGTC | 254065 |
rs746677207 | in-del | -/AAAAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747177 | TGCTCTGAGTTCCTT[-/AAAAC]AATCAACCATTACTT | 254065 |
rs746679085 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768750 | AACCTTAAATGTAAA[A/T]GGGCTAAATGCCCTA | 254065 |
rs746686968 | snp | A/G | 0.000168336 | 0.00917277 | intron-variant | BRWD3 | GRCh38.p7 | X:80725105 | CAATGAAAGCAACAC[A/G]AAATGTTTGGTTCAT | 254065 |
rs746697088 | snp | A/G | 2.29906e-05 | 0.0033904 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682627 | AGCATCATGCTATAG[A/G]TCTGAGAAGGCAGAA | 254065 |
rs746698236 | snp | A/G | 2.5503e-05 | 0.00357084 | intron-variant | BRWD3 | GRCh38.p7 | X:80709384 | GGATGATACAAACTG[A/G]GAAACAAAAAACTAC | 254065 |
rs746704723 | in-del | -/TAT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759086 | GCACAGAGTACAGTG[-/TAT]TATTTTCCTTCATCA | 254065 |
rs746710927 | snp | C/T | 2.30744e-05 | 0.00339657 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80808545 | TTTACTCACCAGATC[C/T]TCGAAGCTTCTTCGG | 254065 |
rs746743978 | snp | C/G | 2.3054e-05 | 0.00339506 | intron-variant | BRWD3 | GRCh38.p7 | X:80688161 | GGGAAAAGACGTTAA[C/G]TTACATTCAAAGTCA | 254065 |
rs746750099 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80750460 | CATACAAATGGCCAA[C/T]GGATATACGAAAAAA | 254065 |
rs746763293 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753707 | TTTTTTATATGGTTA[C/G]AGATACGGGTCCAGT | 254065 |
rs746783547 | snp | G/T | 6.97196e-05 | 0.00590381 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735155 | TGAACAAGATATCTG[G/T]ACTCCAGGTCTGGAT | 254065 |
rs746797485 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781592 | GGCATAGTAGGGGTC[A/G]TGCAGTTGAGATTTC | 254065 |
rs746801851 | snp | A/G/T | 4.5628e-05 | 0.00477622 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734139 | TGACTCTAATTCAGC[A/G/T]ATTTTCTCAGGAACC | 254065 |
rs746810422 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731041 | CAACCTCATACATAT[A/C]TTTGCTGAGTCAGAG | 254065 |
rs746817985 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802541 | GGGGTCATAGTTCTC[C/T]AGATTTCCATGCTGG | 254065 |
rs746819019 | in-del | -/A | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80782565 | AACCCAAATAATGAG[-/A]AAAAATATTTACAAA | 254065 |
rs746827375 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80759984 | CATGCACTGCTAATC[C/T]TCACCTTCCAATTAA | 254065 |
rs746829336 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791322 | GGCGAACTTTAATAT[-/A]AATAGTTTTGTATCT | 254065 |
rs746837642 | snp | C/T | 5.18074e-05 | 0.00508931 | intron-variant | BRWD3 | GRCh38.p7 | X:80687047 | AAGATCTTTCCTTAA[C/T]TCAGTTGATTTTCTC | 254065 |
rs746840513 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700282 | CACAGTAAACACAGT[C/T]CTTTCCCTTCAATCA | 254065 |
rs746850659 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808414 | GGGGAAGGGGCAGTC[A/G]TTCTTTGGCTCTGCA | 254065 |
rs746861977 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729569 | AAAAAGTTAAACATA[G/T]GATGACATTTAATAG | 254065 |
rs746880505 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716872 | GACATTAATTATGTC[-/T]TTTTTTTTTTCTTAT | 254065 |
rs746901862 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741921 | TTAGTTTAATTAGAT[C/T]GCATTTGTCAATTCT | 254065 |
rs746924819 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751406 | AATAAATGAATGAAA[C/T]AAACAAAAAGAGAAG | 254065 |
rs746931977 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695740 | TTATAAGCCACACAC[A/C]ATGTGCATAAGAAAT | 254065 |
rs746947570 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770057 | CTAAACCAGGAAGAA[C/T]TTGAATCCCTGAATA | 254065 |
rs746947615 | in-del | -/TTAA | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80733891 | TCCCACATCATTTAT[-/TTAA]TTATTTTCCAATGGA | 254065 |
rs746954269 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80677428 | TGGTTATTTAGGTTC[-/A]AAAAACAGTCTACAG | 254065 |
rs746979758 | snp | A/G | 2.28804e-05 | 0.00338226 | intron-variant | BRWD3 | GRCh38.p7 | X:80717551 | TTTAAATTTTTTTCT[A/G]AATGTTACCTTATTG | 254065 |
rs746989179 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723520 | ATTTCCTAAGGAATG[A/T]TTATATCTTCATCAC | 254065 |
rs746994293 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772295 | ATGCAGCCATAAAAA[A/C]GTATGAGTTCATGTC | 254065 |
rs747020158 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726831 | ACCAAAATTCTTCCC[C/T]GTGACTACAGAAAAA | 254065 |
rs747035968 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741276 | AGTATTCCATGGTGT[A/T]TATGTGCCACATTTT | 254065 |
rs747062013 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686196 | CGCATGTTCTCACGC[A/G]TAGGTGGGAATTGAA | 254065 |
rs747062171 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697784 | TGACGAACATGCATG[A/T]GCATGTGTCTTCATG | 254065 |
rs747069127 | snp | C/T | 2.32756e-05 | 0.00341134 | intron-variant | BRWD3 | GRCh38.p7 | X:80722793 | GATCTGGAATCTTTA[C/T]GACAGATTTTTAGTG | 254065 |
rs747079361 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766977 | CCGCACCTGTCTCTG[C/T]GAATCCCAAGCCCAC | 254065 |
rs747084622 | snp | G/T | 3.33333e-05 | 0.00408235 | intron-variant | BRWD3 | GRCh38.p7 | X:80703463 | CACAGAAAAAGGTTA[G/T]AACAGGTAATAATTA | 254065 |
rs747084728 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80779269 | GCAGTGAGTCGAGAT[G/T]GTGCCACTGCACTCC | 254065 |
rs747105347 | snp | C/T | 2.32083e-05 | 0.00340641 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723853 | TTTACAATCAAACAC[C/T]GCACCATGGCCTTGG | 254065 |
rs747106377 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757130 | CTTCAAGGTTATGTA[A/G]TAAGTTTTAGTATAT | 254065 |
rs747119750 | snp | A/C | 4.17563e-05 | 0.00456907 | intron-variant | BRWD3 | GRCh38.p7 | X:80745737 | GATATTCACTGAAAA[A/C]AATACGAAATTAACT | 254065 |
rs747140202 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687392 | GAATGATTTTTTTTC[C/T]CAGAAATCCTTTGTG | 254065 |
rs747150043 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80697134 | ACCTATAGAATCAAA[C/T]TCTGTTTGGGGTATA | 254065 |
rs747175231 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80745419 | TACTTATATAAAATG[A/G]GAAACTTTTTTCAAT | 254065 |
rs747185491 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804631 | CACCATTTCAATATA[C/T]AAAACTTATAGATTA | 254065 |
rs747186226 | snp | A/G | 4.58937e-05 | 0.00479007 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686923 | TTCACGTTCATAAAT[A/G]AGGCTCAATAGTTCC | 254065 |
rs747188961 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710253 | TTGTATCTCTAATTG[A/G]AAGCAAGACCCAAAT | 254065 |
rs747203463 | snp | C/T | 0.000155485 | 0.00881579 | intron-variant | BRWD3 | GRCh38.p7 | X:80809414 | CATTCCCTTAGCACC[C/T]CCCCACCCCCCGACA | 254065 |
rs747210290 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80720784 | TAAGCTCCATTCCAT[A/G]GTAAGTGCTTTATAC | 254065 |
rs747275712 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772513 | AGGAGAAATACCTAA[C/T]GTAAATGACGAGTTT | 254065 |
rs747276735 | snp | C/T | 3.39374e-05 | 0.00411917 | intron-variant | BRWD3 | GRCh38.p7 | X:80703621 | TACACGAAAAGTATA[C/T]GTATAAAACACAGTT | 254065 |
rs747278533 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780480 | GGCTAGAAACACATA[C/T]AGGCTATATAAAACC | 254065 |
rs747279768 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678480 | ATTTTTTTAAAAAAA[A/G]GAAATAAAGAGCAGG | 254065 |
rs747284038 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740763 | CAAAACACATCAAAT[G/T]GAAATAAAAAATCAC | 254065 |
rs747305209 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80683791 | AATTACTACCTCTCC[-/T]TCTCCTTGTTTTTTC | 254065 |
rs747328189 | snp | C/G/T | 0.000120919 | 0.00777481 | intron-variant | BRWD3 | GRCh38.p7 | X:80691177 | GGCTGGCAAAATCTA[C/G/T]AAAATTATGAAAATC | 254065 |
rs747335848 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731819 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 254065 |
rs747338679 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80794809 | AATCAAAAAAGCACA[C/T]AGGTGATGAGTAAAC | 254065 |
rs747351690 | in-del | -/CTGT | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80785037 | AGCTCAGCAGCAGAA[-/CTGT]CTGTGTGAAATTTTA | 254065 |
rs747380720 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701384 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAT | 254065 |
rs747394083 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80805482 | TCTTTCCTTTTCATA[A/C]CCCAATACACCTTAA | 254065 |
rs747401442 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770688 | TCCCTTTGAAAACTG[C/G]GACAAGACAGGGATG | 254065 |
rs747418613 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80693160 | TGTATCTAGCATTAT[A/G]AGAAGCTTCCATCTA | 254065 |
rs747420128 | snp | A/G | 2.2849e-05 | 0.00337994 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709474 | CCTGAATTTTGACAT[A/G]ATGCCTGTGAATTAT | 254065 |
rs747427623 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712747 | TGAGATGTGGGGAGC[A/G]CCTCTGCCCTGCCGC | 254065 |
rs747429018 | snp | A/C/T | 0.000427506 | 0.014614 | intron-variant | BRWD3 | GRCh38.p7 | X:80744305 | CAGAAATTCACAATA[A/C/T]CCCCACCCAAAAAAT | 254065 |
rs747431319 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702173 | ATAAAAAGTGTATGT[C/T]TGCCTTTATAATTTC | 254065 |
rs747433365 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794297 | GATGGCTTGAGCCCA[G/T]GAGTTTGATAACAGC | 254065 |
rs747439210 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747400 | CCCCACACTAAGTCG[C/T]GACAAACAAAAATAT | 254065 |
rs747466125 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785934 | ACTTGGGAGGTTGAC[A/G]CAGGAGAATCACTTG | 254065 |
rs747470856 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773994 | GTGTTCACGTATTTG[C/T]TGAATTGAATAAAAC | 254065 |
rs747473867 | in-del | -/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80732868 | ATGTTGGCCGGGCAT[-/G]GTGGCTCACGCCTGT | 254065 |
rs747484494 | snp | C/T | 2.29208e-05 | 0.00338524 | intron-variant | BRWD3 | GRCh38.p7 | X:80681992 | AAAACAAAAGACATA[C/T]TTACCAGGAGATGAG | 254065 |
rs747514098 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711793 | TGACCTGGAACCTCC[-/T]CCGTCACACCCCCAT | 254065 |
rs747525958 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754463 | GCAAACAGAGATAAT[C/T]TGACTTCCTCTTTTC | 254065 |
rs747530517 | in-del | -/ATAAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725821 | GTGTTACATGCCTAT[-/ATAAC]ATAACATGTTTACAT | 254065 |
rs747533503 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80753570 | GCCACCACACCCAGC[C/T]TTGAGGTCTTACTCA | 254065 |
rs747554283 | in-del | -/GGCTC | 0.00034229 | 0.0130778 | intron-variant | BRWD3 | GRCh38.p7 | X:80703442 | AGTTAGTGCTCTTGA[-/GGCTC]GGCTCCACAGAAAAA | 254065 |
rs747572830 | snp | A/G | 2.28537e-05 | 0.00338029 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681416 | TTCCACTTCGGCTAT[A/G]TCCACCGAAGCTCGA | 254065 |
rs747594729 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807459 | AATCATTTATATTTA[A/G]AGTCTATCATACACC | 254065 |
rs747594913 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753350 | TCTCGGCTCACTGCA[A/G]CCTCTACCTCCCAGG | 254065 |
rs747603128 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743076 | ATACATCCCATGAAT[A/T]CCTAATTTATTGAGA | 254065 |
rs747620728 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759573 | TATTATTCTCTCCAG[A/C]TCTTACGTTTTAGCT | 254065 |
rs747620873 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737156 | AGAAACCAGGACTCA[C/T]GCCTATATAGTCCTC | 254065 |
rs747627210 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715671 | TTGCAAGTCATACAA[C/T]CTCTGTTACAACTAT | 254065 |
rs747629059 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80692817 | AAATTTCTTCTTTAC[A/G]GGTACAGGTATTGTG | 254065 |
rs747652821 | in-del | -/A | 0.000142454 | 0.00843839 | intron-variant | BRWD3 | GRCh38.p7 | X:80691038 | TTATAATAAGTGATT[-/A]AAAAAAAAACAGACC | 254065 |
rs747667449 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80738891 | ATGAGATTGAAGAGC[A/G]CCAAGGAGGCTGAGA | 254065 |
rs747687887 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716776 | AATAATGCCACATTT[A/T]ACAGTGGTATACAAA | 254065 |
rs747690896 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752813 | GGGATTACAGGTGCC[C/T]GCCACCACACCCAGC | 254065 |
rs747693203 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80774183 | CTTGCTTCTTAGTTT[C/T]GCATATATATTTTTG | 254065 |
rs747696753 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784711 | TGTCCCTGCAAAGGA[C/T]GTGATCCCATTCCTT | 254065 |
rs747713839 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763381 | ACCCCAATAGCTAAC[C/T]ATGTTTCAGTGACTA | 254065 |
rs747735762 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80708357 | GCTGAGATTGAGCCA[C/G]TGTACTCCAGCCTGG | 254065 |
rs747736085 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725725 | ATAACATATAACATG[C/T]TTACATGTGTTACAT | 254065 |
rs747737030 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736338 | GTTATAAAAAAATTA[C/T]TTTTAAATTATTTAA | 254065 |
rs747754613 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703240 | GACTTCACAAGCTGA[C/T]TAATTTATCTCAATA | 254065 |
rs747762829 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809592 | GCTTCCGCCGCACTC[C/G]TCGTCCTAGTTTCGC | 254065 |
rs747767480 | snp | A/G | 2.28256e-05 | 0.0033782 | intron-variant | BRWD3 | GRCh38.p7 | X:80682453 | AAAAATGTTGCATCA[A/G]TGTAATGATACCTAG | 254065 |
rs747773335 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80682395 | CCAAATTATTCATAA[A/T]CTTTCACAAATTAGG | 254065 |
rs747775849 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810065 | GCTAACTGACGGCCG[A/T]CGCTCTGGCAGCCGC | 254065 |
rs747788813 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80704054 | GGGAAAAGAAACTGT[C/T]ATTGGGATGAAATAA | 254065 |
rs747823801 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675803 | GTGATAGGAAAAAAA[C/T]TGATGCGGGAAACTT | 254065 |
rs747838508 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805849 | CTGAAGCAGGAGAAT[A/C]GCTTGAACCTGGGAG | 254065 |
rs747841394 | snp | C/G | 2.29179e-05 | 0.00338503 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686891 | AGATCAGCTGGCTGT[C/G]GAAATGGCTCCGAGT | 254065 |
rs747841841 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678669 | ATGTTCAAACATTTA[A/C]AGATAAAGAAGAACC | 254065 |
rs747856962 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715762 | TGTGTTCCAATAAAG[A/G]TTAACAGAAATAGGT | 254065 |
rs747876714 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743898 | ATATCTTGCTGCAGG[A/G]TAGGAGCAAAGTCCA | 254065 |
rs747880792 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768245 | CACCACAAAGATACT[C/T]CTTGAGAAAATCAAC | 254065 |
rs747883826 | snp | A/C | 4.9087e-05 | 0.0049539 | intron-variant | BRWD3 | GRCh38.p7 | X:80703609 | CTAAAACATAAATAC[A/C]CGAAAAGTATATGTA | 254065 |
rs747907868 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749766 | CAAGTGAAACCAGAA[A/C]AGACCCCAAACAGCT | 254065 |
rs747917743 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699397 | GTGGTGTATGTATAC[A/C]TATGTCTGTCTGTAT | 254065 |
rs747921506 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780971 | ATGAAGAGTGACATA[C/T]AACGACACAATGGCC | 254065 |
rs747925384 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695655 | ATTTTAGGGCAACAG[A/C]CATTTGAGAATTTTC | 254065 |
rs747935115 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737191 | GGTATCATTGAGACA[C/T]TGCTTCCAGGACCTC | 254065 |
rs747948131 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751265 | GTAATGTTCTCACCA[C/T]AAGAAAATGTTGGTG | 254065 |
rs747970135 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767971 | GATCAATTGGAAGGA[A/G]GGGTGGTTATCAGTG | 254065 |
rs747970379 | snp | C/T | 3.37115e-05 | 0.00410543 | intron-variant | BRWD3 | GRCh38.p7 | X:80703450 | GCTCTTGAGGCTCCA[C/T]AGAAAAAGGTTATAA | 254065 |
rs747987301 | snp | C/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669135 | ATAATTCTCTGAGAA[C/T]TTCTGCTTGAATACT | 254065 |
rs747996848 | in-del | -/C | 0.00158814 | 0.0281345 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810229 | TGACTCGACTCCTTT[-/C]CCCCTTTTTCCTCCC | 254065 |
rs748012185 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709256 | ATCCAAGACATCTAA[A/G]TGAATTAAATATGCC | 254065 |
rs748013186 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805892 | GTGAGCCGAGATCCC[A/G]CCACTGCACTCCAGC | 254065 |
rs748013950 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789641 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 254065 |
rs748046889 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80700172 | AGAAAGAAATAATTA[C/T]AATATTGAAAGACTT | 254065 |
rs748065840 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687942 | TAAATATTATCAATG[A/G]GCATACCTAATATAC | 254065 |
rs748086008 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740861 | GGCAAACATCTTGCA[-/T]TAAATATTAATACAA | 254065 |
rs748097172 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon | BRWD3 | GRCh38.p7 | X:80676702 | AAGATTCAGAGGATC[C/T]TCAGTGGACACAAAA | 254065 |
rs748108760 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80718000 | TTTTCAAAGTAGTTT[C/T]ACATCTGACATCTAC | 254065 |
rs748114483 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767446 | TCCAGCAAACACCAA[A/C]AGACCTGCAGCTGAG | 254065 |
rs748117835 | in-del | -/A | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669222 | AGTCTTAAATTTTTG[-/A]AAAAAAACGGAAAGC | 254065 |
rs748117945 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755950 | TGAAGCCAACTGCTT[C/T]GTGTTAAAAGAATGA | 254065 |
rs748118304 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786298 | CAGTTAAAATATGCC[C/G]TGAAAAATTACTGAT | 254065 |
rs748133417 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80728583 | TTTTAGCAGGTATAG[C/T]GCGTGTCATCCCTAT | 254065 |
rs748138055 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734548 | AATTCTCTTTACTGT[C/G]GTTATAGTGGTTGAG | 254065 |
rs748163835 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80694191 | GTGTAAGCCCCAAAC[C/T]TTGATGGCTTCCATG | 254065 |
rs748163895 | snp | A/C | 2.28773e-05 | 0.00338203 | intron-variant | BRWD3 | GRCh38.p7 | X:80734106 | AAGCAACCGTTTCTG[A/C]TTTTCTCTTACCGTA | 254065 |
rs748174087 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80749427 | CTTGATGAACTAACA[A/T]CTCTATCATTACATA | 254065 |
rs748177370 | snp | C/T | 2.28438e-05 | 0.00337955 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744117 | ACTCTTACTACCTTA[C/T]CACAGCTGCCTGCAG | 254065 |
rs748179755 | snp | G/T | 2.28438e-05 | 0.00337955 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681388 | GATTTGGCTTTCCCT[G/T]GGTCATGGCTATTTC | 254065 |
rs748186131 | snp | A/T | 2.48574e-05 | 0.00352535 | intron-variant | BRWD3 | GRCh38.p7 | X:80687027 | TTTAATAGAGTTATA[A/T]CTAAAAGATCTTTCC | 254065 |
rs748198903 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788041 | GTGAGCCGAGACTGC[A/G]CCACTGCACTCCAGC | 254065 |
rs748200558 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778657 | AATAACCTTGGATTC[A/G]TATTTTCTCTTTTAC | 254065 |
rs748225469 | snp | C/T | 0.000233448 | 0.0108014 | intron-variant | BRWD3 | GRCh38.p7 | X:80722512 | AGAGAACAGCAGTAA[C/T]GTATAACATTGGGCA | 254065 |
rs748233792 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710077 | GAAAAGGGCACCATC[A/G]GAGCTTGCAGCTCAT | 254065 |
rs748238555 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80780216 | CTATAAAGTACTGAG[C/T]TAAACATATAGAACA | 254065 |
rs748264965 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685327 | AAAAAATAAATGACC[-/A]AAAAAATCAAACAAA | 254065 |
rs748267467 | snp | A/C | 2.28728e-05 | 0.0033817 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691106 | GAGGTCAGTTGGATA[A/C]GCAACTACAGTACAA | 254065 |
rs748267732 | in-del | -/C | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80765653 | CAGTTTCTTTGCTTT[-/C]CTTTATCATGTAAAA | 254065 |
rs748302462 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680313 | TAATTGATGTCCCTT[A/G]TATGGTCCAAGATAG | 254065 |
rs748325584 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778319 | AAATCCTGTAACCAA[C/T]TTCAAGACAAAGTTT | 254065 |
rs748375802 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719768 | AAAACAGCATTAAAC[A/G]TAAAATAAAGTATAT | 254065 |
rs748377545 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746059 | TAAATCTTTCTATAA[C/T]ATGAAGAAATTTTAG | 254065 |
rs748396527 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80726296 | GTATAACATATAACA[C/T]GTTTACATGTTATGT | 254065 |
rs748421788 | snp | A/G | 2.28441e-05 | 0.00337957 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722754 | CACGAATAAGAGGAC[A/G]ATAATCCGTGTGGAA | 254065 |
rs748438526 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792945 | GAGGCAGGCGGATCA[C/G]GAGGTCAAGAGATCA | 254065 |
rs748442595 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686730 | CACTAATCACACTAC[C/T]ACTTTCACAATCAAA | 254065 |
rs748445013 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790298 | AGCTATAGAGAACTA[G/T]GACCCACAAAGAGAA | 254065 |
rs748449195 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770223 | TCCAATCAATAGAAA[A/C]AGAGGGAAACCTCCC | 254065 |
rs748482665 | snp | A/G | 2.54965e-05 | 0.00357038 | intron-variant | BRWD3 | GRCh38.p7 | X:80707511 | TCATCTTCCTACAAC[A/G]AAGAGCCAGCAATTA | 254065 |
rs748486311 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80745048 | ATACTGGTGTACTAC[A/G]ATTTTGTACTCAAAA | 254065 |
rs748541232 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722971 | AATGGTAATTCTCTT[C/T]TCTCCACAAAATCCT | 254065 |
rs748550402 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769648 | GAAAGCAGGAAAGAT[A/C]TAAAACTGACACCCT | 254065 |
rs748565466 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80783964 | TGGGGATGGTTAATG[C/G]GTAAAAAAATATAGT | 254065 |
rs748569503 | snp | A/G | 4.5597e-05 | 0.00477456 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677075 | TTTCTTTTAGGTCTG[A/G]TTTGTATGAATTTGC | 254065 |
rs748571963 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720614 | AGTAAGCTAAGGTTA[A/C]TTTGTTACTGAAGAA | 254065 |
rs748572797 | snp | C/G | 0.000136996 | 0.00827521 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728873 | GTCACCTTAAGTTTA[C/G]TGATCTTGTCTTCTC | 254065 |
rs748577922 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764020 | TGAGGAGATAAACAC[A/G]CAAATCAATGGAACA | 254065 |
rs748579945 | in-del | -/A | 6.93963e-05 | 0.0058901 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704630 | TAAGTTATCAAAGGC[-/A]AAAAAACAAAAAATA | 254065 |
rs748582877 | snp | C/G | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792419 | TGTCATAACAGATAA[C/G]AGCACTGCATATCAG | 254065 |
rs748590330 | in-del | -/AT | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80803530 | AAATCGCTAAAGCCA[-/AT]ATATTTCAGAGAGCG | 254065 |
rs748594962 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711709 | AGACATTTCCTTCCA[C/T]TGATTCTAGGTCTTT | 254065 |
rs748598308 | in-del | -/TG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726106 | CATGTTTACATGTTA[-/TG]TGTCTGTATAACATA | 254065 |
rs748615653 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686067 | ATTCCATGGTGTATA[C/T]GTGCCACATTTTCTT | 254065 |
rs748632901 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712299 | GATTGCAGGCACGCG[C/G]CGCCACACCTGACTG | 254065 |
rs748635655 | snp | A/G | 2.39719e-05 | 0.00346199 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677316 | TCTTGATTCCTGTCC[A/G]GGGCTCTCTGCCATC | 254065 |
rs748644686 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731660 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 254065 |
rs748647459 | snp | A/G | 2.37107e-05 | 0.00344308 | intron-variant | BRWD3 | GRCh38.p7 | X:80709421 | TAAATAATAGTATAT[A/G]TATAACCTCTGAAGA | 254065 |
rs748659071 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739646 | GTAGACCCTCCTTAT[A/C]TGCAGAGGACACATA | 254065 |
rs748679982 | in-del | -/AT | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80725974 | ACATAACATGTTTAC[-/AT]GTTATATGTCTATAT | 254065 |
rs748725468 | snp | C/T | 2.35666e-05 | 0.0034326 | intron-variant | BRWD3 | GRCh38.p7 | X:80691007 | AAAGGAAAGCAAAAG[C/T]CATAAAGCTATAAAT | 254065 |
rs748728422 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756427 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTAGC | 254065 |
rs748734888 | snp | C/T | 0.000116102 | 0.00761824 | intron-variant | BRWD3 | GRCh38.p7 | X:80734079 | TAAGCTTTCCAAGGA[C/T]GTTCAAAAATAAAGC | 254065 |
rs748751743 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80762475 | ACCAAATAAAAGATA[C/T]TAATGGATCTAAAGC | 254065 |
rs748762713 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751791 | CCACATTTTGTAGCA[-/C]CCACTTATGAGTTCA | 254065 |
rs748763288 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80690720 | CTGACCAAATTCTCC[A/G]ACAGAGGATTTAAAC | 254065 |
rs748780123 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675253 | TGAGTGTGCAGTGCA[A/G]TAAGGTTCTTTCCTG | 254065 |
rs748808774 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733671 | TATTGGCAGTAACAG[C/G]AAACAAACCAGACAT | 254065 |
rs748836306 | snp | G/T | 1.65927e-05 | 0.00288029 | intron-variant | BRWD3 | GRCh38.p7 | X:80730046 | TTAAAATAACTTTAT[G/T]AATTTTCTCAAAAAT | 254065 |
rs748841794 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80761357 | CATTACCTTCTATTA[C/T]CTTCATGCATGAAAA | 254065 |
rs748844447 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792917 | GCCTGTAATCCCAGC[A/T]CTTTGGGAGGCTGAG | 254065 |
rs748850200 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805357 | TCAAATGAAAGTATA[C/T]ATATGAACAAAAAGG | 254065 |
rs748853109 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758034 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAG | 254065 |
rs748859969 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742950 | AATAGGAGTGGTGAG[-/A]AGAGGGTATCCCTGT | 254065 |
rs748883349 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712204 | TGATGCCGAGCCGAA[-/T]GCTGGACTGTACTGC | 254065 |
rs748889698 | in-del | -/ATATATATATATATATAT/ATATATATATATATATATATATATATATAT | 0.0475538 | 0.146682 | intron-variant | BRWD3 | GRCh38.p7 | X:80700433 | GATTGAAAATATTTG[lengthTooLong]ATATATATAACAATA | 254065 |
rs748891919 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784712 | GTCCCTGCAAAGGAC[A/G]TGATCCCATTCCTTT | 254065 |
rs748943681 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701226 | TTTCTATATTTATTA[C/T]AAAAAGTTTCTTTTC | 254065 |
rs748946317 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725627 | CAATGCTTTATGTTA[C/T]ATGTCTATATAACAT | 254065 |
rs748958380 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724439 | GTAGTCCCATCACCA[C/T]AGAAGGGTGTTCTGA | 254065 |
rs748959587 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772399 | CGCATGTTCTCACTC[A/G]TAGGTGGGAATTGAA | 254065 |
rs748966948 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698430 | AAGTAAGAACTTGGC[C/T]GGGTGAGGTAGCTCA | 254065 |
rs748972014 | snp | G/T | 4.25686e-05 | 0.00461329 | intron-variant | BRWD3 | GRCh38.p7 | X:80696895 | CAATAAATTATTACT[G/T]TCAATATAATTACTT | 254065 |
rs748982303 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670435 | TTTCTTGACCTTCTC[A/C]ACTTGGAAAAAAAAT | 254065 |
rs748990050 | snp | C/T | 2.33918e-05 | 0.00341985 | intron-variant | BRWD3 | GRCh38.p7 | X:80716129 | TCTGCAAATAGTGTA[C/T]CCCAAAGTATTGTAA | 254065 |
rs748995877 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808737 | CGGCCTGATAGCTAT[A/T]GGCTCAGAGCTAGAC | 254065 |
rs749020327 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673453 | TCCATACAAAATGTT[A/C]TCTTTTTTTGAATGT | 254065 |
rs749029113 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735349 | ATTCTCATCAATTAG[C/G]TTAAAAATGCATTTA | 254065 |
rs749046701 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766295 | CTTTTGGACTTGGAC[A/G]GGATCTTATACCACC | 254065 |
rs749057155 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80682269 | CAATCATTAAAATTT[A/T]AAAAAAGTTTCTGGG | 254065 |
rs749060284 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719656 | ACTACCTCACCATCA[C/T]CTTAATAAGACCAGA | 254065 |
rs749060984 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743837 | TAAATCATCTTTTTA[G/T]TTATTTATTAAAAAA | 254065 |
rs749062602 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789122 | ACTCTATCTTTGGAG[C/G]TCTCTAGGTATAAAT | 254065 |
rs749062660 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799546 | GGTTGATTGATTTAG[A/G]GGACAGAACAGGCAT | 254065 |
rs749063127 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715507 | TTGGTGTACCTGAGA[C/G]TATTCTGCTTAGCAG | 254065 |
rs749087968 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707272 | AGAAAGGTATTGGGA[G/T]AGCCAGGATCACATC | 254065 |
rs749089030 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773978 | GCTTTACATATATTT[A/G]GTGTTCACGTATTTG | 254065 |
rs749099024 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767093 | GAGGCTTAAGTAGGT[A/T]AACAAAGCCACAGGA | 254065 |
rs749100453 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80691651 | AAATTATCAGTTATT[A/C]CTTTGGCCAAGCATA | 254065 |
rs749139449 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715637 | CTGCAAAGGACCAAA[A/G]TGTAAACATTTTTTG | 254065 |
rs749153794 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798559 | CTGACTCGGAACAGT[C/T]AAGTGCTCTGAGGCC | 254065 |
rs749168151 | snp | G/T | 0.00211696 | 0.0324653 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810010 | ACTCTCCCGGAGCCC[G/T]ATGGTTGCTTAGCTA | 254065 |
rs749189863 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789532 | AGGCGCGTGCCACCA[C/T]GCCCAGCTAATTTTT | 254065 |
rs749190287 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697873 | CTTTAAGTCTCCTGA[A/G]AAATCTCCAGATTGC | 254065 |
rs749205816 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727734 | GACAAGTTGAGATTG[G/T]GTAATTCCTACTTAT | 254065 |
rs749210580 | snp | A/G | 2.99213e-05 | 0.00386778 | intron-variant | BRWD3 | GRCh38.p7 | X:80685576 | GGTTTCCAGACAACT[A/G]TAACAAAATATCAAG | 254065 |
rs749219296 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736592 | TTCAATTGAAGTATA[C/T]AATTTTGTCTTTTTT | 254065 |
rs749224347 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736169 | GTATTTTCAAATTGT[A/G]ATCATTTAACAAATA | 254065 |
rs749274646 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679520 | ATATGCATTTGGAGA[A/G]TCATCACATCAAGAT | 254065 |
rs749280645 | snp | A/C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80741162 | AGAACATGCGGTGTT[A/C/T]GGTTTTTTGTCCTTG | 254065 |
rs749282211 | in-del | -/TC | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671048 | TCATCTCACCTCACT[-/TC]TCTCTCTCCTACACT | 254065 |
rs749290842 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758082 | CGCATGACTGTAATC[C/T]CAGTTACTCGGGAGG | 254065 |
rs749298460 | snp | C/T | 3.29908e-05 | 0.00406132 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80684161 | ATAACATCTTGATAA[C/T]CCTACAAAGAAGAAT | 254065 |
rs749306691 | snp | C/T | 0.000434726 | 0.0147368 | intron-variant | BRWD3 | GRCh38.p7 | X:80703436 | TGATTAAAGTTAGTG[C/T]TCTTGAGGCTCCACA | 254065 |
rs749317894 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80764458 | CTACAGGCACCTGCC[A/C]CCACGCCTGGATAAT | 254065 |
rs749326496 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726795 | TCCCCTTATGATAAG[A/T]ACCATCACAACTCAA | 254065 |
rs749329702 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688903 | GAAACTATAATAATA[A/T]CTAATTGGTATATCA | 254065 |
rs749333817 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771717 | TTTTGCAACCTACCC[A/T]TCTGACAAAGGGCTA | 254065 |
rs749335704 | snp | C/T | 2.5041e-05 | 0.00353834 | intron-variant | BRWD3 | GRCh38.p7 | X:80690116 | GAAAAAATACTCTGT[C/T]AGCCTTGGCTAATAT | 254065 |
rs749346429 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796162 | TTGAGTCGGAGTCTC[A/G]CTCTGTCACCCAGAC | 254065 |
rs749346729 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751190 | ATTTACTGTACTACA[C/T]GGTGACCACAGTTAA | 254065 |
rs749361820 | snp | A/G | 3.29723e-05 | 0.00406018 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80689813 | TGCTTTAATTTTATT[A/G]TAAGTATCCAGTATA | 254065 |
rs749366665 | snp | A/T | 0.000288184 | 0.0120004 | intron-variant | BRWD3 | GRCh38.p7 | X:80736092 | TGATGGACAAAACTT[A/T]AAAAAAAAAAAATCT | 254065 |
rs749385223 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728129 | ATGGCAACCATTTGG[A/C]ATTCTCTCCTTAAAA | 254065 |
rs749411347 | snp | A/C | 5.0072e-05 | 0.00500335 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707500 | TGCCAACAGTTTCAT[A/C]TTCCTACAACAAAGA | 254065 |
rs749412550 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694471 | GAATGGCAGATCCAC[C/T]GACAACGTGCGCCGT | 254065 |
rs749415832 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713495 | TGCTTGAAGGCAGCA[C/T]GCTCCTTAAGAGTCA | 254065 |
rs749434547 | in-del | -/CA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771644 | ACTAAAGAGCTTCTG[-/CA]CACAACAAAAGAAAC | 254065 |
rs749447682 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749425 | TTCTTGATGAACTAA[A/C]ATCTCTATCATTACA | 254065 |
rs749447804 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777104 | TTTTGAATTATCCTA[C/T]AGATTCAGCAGTTTC | 254065 |
rs749449429 | snp | C/T | 4.56924e-05 | 0.00477955 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681367 | GGCAAAACTCTATTC[C/T]GAAATGATTTGGCTT | 254065 |
rs749463787 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783385 | AGTGAGACCCTGTCT[-/AA]AAAAAAAAAAAAAAA | 254065 |
rs749506906 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795608 | ACAATAGGCTGGGAA[C/T]GGTGGCTCATGCCTG | 254065 |
rs749511326 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80734457 | ATCATAAACATTAAA[A/G]AACACATCCTGAGGA | 254065 |
rs749511453 | snp | A/C/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80726080 | ATGTTTACATGTTGT[A/C/G]TGTATAACAACATGT | 254065 |
rs749513600 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695274 | TTTCTTTATAAATTA[-/C]CCAGTCTCAGGTAGT | 254065 |
rs749531922 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706368 | TCCACCTCGGCCTCC[-/A]AAAGTGCTGAGATTA | 254065 |
rs749542343 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713674 | TCTGCGAGAGACACC[C/T]AAGAATGATCAATAA | 254065 |
rs749560929 | snp | C/G | 2.2915e-05 | 0.00338482 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744078 | TGAAGGACTGCAACG[C/G]GTGCACAAGTTCGAA | 254065 |
rs749565253 | snp | A/C | 2.45827e-05 | 0.00350582 | intron-variant | BRWD3 | GRCh38.p7 | X:80717785 | AACAAGGAAAATTAT[A/C]ACTTTGTGAGCAAAG | 254065 |
rs749565398 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80765284 | CCATATTGATTGACA[C/T]TGACTACTGAGAGGA | 254065 |
rs749592113 | snp | C/T | 2.35871e-05 | 0.0034341 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677280 | TGTTTTCATCTTCTT[C/T]TGATGCACTAAGTAG | 254065 |
rs749607717 | snp | A/G | 2.28841e-05 | 0.00338253 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682599 | ATGACTTTCAAATAA[A/G]GCAGATAATCGCAGC | 254065 |
rs749612273 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778226 | TCAATCCAACTTTAG[C/T]AGGCCAGAATTTTGG | 254065 |
rs749629780 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80787841 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 254065 |
rs749630984 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762351 | CCTAAGTCCTAAAAG[C/T]GATAAGTGACAGAGA | 254065 |
rs749640761 | snp | G/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811336 | AGAAATGTTTTGGAT[G/T]TTGGACTTTTTCAGA | 254065 |
rs749645235 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80685207 | TGTGTAATTGATGTT[C/T]TCTACTCTGCTGCAG | 254065 |
rs749655558 | snp | C/T | 2.38158e-05 | 0.0034507 | intron-variant | BRWD3 | GRCh38.p7 | X:80725090 | AAAAATCAGTATTAA[C/T]AATGAAAGCAACACG | 254065 |
rs749667916 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768967 | ATAAAACAGACTTTA[A/C]ATCAACAAAGATCAA | 254065 |
rs749668593 | snp | G/T | 7.02333e-05 | 0.00592552 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80791992 | TAAGGAATAGAGCAG[G/T]TTTTTTTTTAACCAT | 254065 |
rs749677290 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755742 | TACAAGTCCAGTATC[A/G]AGGGAATGGTTACGT | 254065 |
rs749678821 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777150 | CTCTTAAGACCCCCC[C/G]CCACGAAAAACCTCC | 254065 |
rs749686782 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711568 | GGAGAGAATCAACCA[A/G]AAGTCTGGCACTTTT | 254065 |
rs749693686 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80787228 | AAAGATTTACAAAAA[C/T]AAAGAGCTATACTAC | 254065 |
rs749695198 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684366 | CCTTAGCCCTCACAC[C/T]ACAGTAATAACCGTA | 254065 |
rs749699217 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718656 | AATTTTATGAGATAT[C/T]GAAGACATCAGGAAA | 254065 |
rs749708092 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669041 | GAAGAGAACAGGCTA[A/C]AACTGCCCACTGGTA | 254065 |
rs749719502 | snp | C/T | 0 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791867 | ACCCACATTTGGAGG[C/T]TTCACATAATTTACA | 254065 |
rs749719908 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740884 | TAATACAAGGTATGC[A/C]AATATTCAAGTTAGA | 254065 |
rs749737453 | in-del | -/TTTTTAAAAACCTTAAGTTAGA | 3.05199e-05 | 0.00390628 | intron-variant | BRWD3 | GRCh38.p7 | X:80689917 | TTTTTTAAAATTAAT[-/TTTTTAAAAACCTTAAGTTAGA]CTCTCTGGAAGCTAA | 254065 |
rs749740989 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708395 | AACAAGACTCTTGTC[-/T]TTTTTTTTTTTTTTT | 254065 |
rs749790491 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80760376 | CCTCCAATTATATCA[C/T]GAACATAGCAAAGAA | 254065 |
rs749813087 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680910 | TACTCCTGGCTAAAG[C/T]GCTCCTCCCACCTCA | 254065 |
rs749849831 | snp | A/T | 2.29618e-05 | 0.00338827 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728827 | CACTGCAGTAATAAC[A/T]GTGGTATCATAGCGA | 254065 |
rs749851147 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746449 | AAAAAAAGCCATAAC[A/G]TAGCATAAGTCTACA | 254065 |
rs749871336 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791940 | GACCCATTCCATAGT[A/G]TACTCTTACAGTCTA | 254065 |
rs749871351 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80803081 | CCTTCCAGCCTGGGC[A/G]ACAGCGCAAGACTCC | 254065 |
rs749891170 | snp | A/G | 2.34819e-05 | 0.00342643 | intron-variant | BRWD3 | GRCh38.p7 | X:80723740 | CAGCAAAATTTAAAT[A/G]TGCTAACCTTTTCGT | 254065 |
rs749894413 | snp | A/G | 3.26174e-05 | 0.00403827 | intron-variant | BRWD3 | GRCh38.p7 | X:80700083 | AAACAGAAAACATAA[A/G]GTATTAAACAGCAGC | 254065 |
rs749895824 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757333 | TAGCCAGGAAAACAA[C/T]GTGTGCTTCTTCACC | 254065 |
rs749905017 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746773 | AGCTAGATTAGTATG[A/T]TTAGAACCATGCCAC | 254065 |
rs749906339 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788391 | CAATAATAAAAAAAC[A/G]CAAACAACTCAATTT | 254065 |
rs749932873 | snp | A/G | 2.27964e-05 | 0.00337605 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722635 | TGGTACCAACCGTTG[A/G]AATTTTGTGGGATGA | 254065 |
rs749935506 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697538 | GTCCAGTTGTACCAA[-/C]TGTTTAGTACCCATT | 254065 |
rs749937613 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685894 | CTGTACCTCTTCTCT[A/G]AGAAAGTTAAAATAG | 254065 |
rs749941576 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80778860 | AAAAATTAGCTGAGC[A/G]TGGTGGTGCACACCT | 254065 |
rs749953464 | in-del | -/AT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726386 | TTATATCTGTATAAC[-/AT]ATAACATGTTTACAT | 254065 |
rs749954356 | snp | A/G | 6.90695e-05 | 0.00587622 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80724972 | GGTCCCCCGGTCAAG[A/G]TCCCAAATAAAAATG | 254065 |
rs749960163 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748313 | CCACTGCACCCAGCC[G/T]TTTGCATCTATTCTC | 254065 |
rs749981528 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669584 | TTACACAATTTGTTA[C/T]GCAAATTTCATTTAA | 254065 |
rs749987503 | in-del | -/AACAA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740735 | CATGGGTGACAACAA[-/AACAA]AACAAAACAAAACAA | 254065 |
rs749988105 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80686199 | ATGTTCTCACGCATA[A/G]GTGGGAATTGAACAA | 254065 |
rs749989423 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80719416 | CGTAAAATATTTTCC[A/G]TGTAATTATTTGGTA | 254065 |
rs750002033 | in-del | -/C | 0.000575126 | 0.0169479 | intron-variant | BRWD3 | GRCh38.p7 | X:80809412 | CCCATTCCCTTAGCA[-/C]CCCCCCACCCCCCGA | 254065 |
rs750016415 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712095 | GTCCAATCTCCAACC[C/T]CCCACCTCTGAAATA | 254065 |
rs750044344 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80804345 | AGGGCTCAAGCAATT[C/T]TCATGCCTCAGCCTC | 254065 |
rs750047563 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738875 | AACAAACACGCAGTA[A/G]ATGAGATTGAAGAGC | 254065 |
rs750068241 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765350 | AGAATGTCTGAAATA[A/C]AAGAGCTCCTTTAGA | 254065 |
rs750077532 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675322 | CAGAATCTATAAGTT[A/G]ATTCATAATACTAGC | 254065 |
rs750080794 | snp | A/G | 2.31377e-05 | 0.00340122 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686975 | TCAGGATTACACTTT[A/G]AAGACTGTCTTCTGC | 254065 |
rs750102748 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80720318 | CGGAAGACCTTCCAG[A/T]GGGACAAGCAAGATG | 254065 |
rs750122635 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763051 | TTGCTGCCCAGAGTC[C/T]ATGATATATTTTTTA | 254065 |
rs750136849 | in-del | -/AG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727091 | GAACAAGATCTAGTC[-/AG]AATCAGTAATGTCTT | 254065 |
rs750143811 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80770020 | AATGGATAAATTCCT[C/T]GACACATACACCCTC | 254065 |
rs750144951 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757913 | TGATTATAAACAAGT[C/G]AAATAGGCTGGGCGC | 254065 |
rs750161557 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80703011 | TAATAAATATGGCTA[A/C]ACTCATCAATCACAG | 254065 |
rs750170357 | snp | A/C | 7.86287e-05 | 0.00626962 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685534 | CTCTTGCTCCTGATG[A/C]CCCTATTAGGGTGAA | 254065 |
rs750171061 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752520 | TTATAATCCTACCAA[C/T]AGTGTGTTAAGAGTT | 254065 |
rs750177979 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775382 | CCACTACTTATTTTT[C/G]AAGGGGCTTTACTTG | 254065 |
rs750185154 | snp | A/C | 2.30723e-05 | 0.00339641 | intron-variant | BRWD3 | GRCh38.p7 | X:80691048 | GTGATTAAAAAAAAA[A/C]AGACCTGTAAAAGCG | 254065 |
rs750186923 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703125 | GTTGAACGTGTTTTG[-/T]TTTTTTTTTAATAAA | 254065 |
rs750204602 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784539 | CTGATGCTTTCCCTT[C/T]CCTCACCCCCACAAG | 254065 |
rs750220346 | snp | C/T | 7.42005e-05 | 0.00609055 | intron-variant | BRWD3 | GRCh38.p7 | X:80744029 | TTTTATCACTTTTCT[C/T]ACCTGTATGGAAGTA | 254065 |
rs750225165 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793925 | GGCTCACGCCTGTAA[A/T]CCCAAAACTTTGGGA | 254065 |
rs750244568 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759137 | AATGAAGGTTAAGAT[C/T]GCAAAGACTACATTA | 254065 |
rs750258906 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762363 | AAGCGATAAGTGACA[C/G]AGAAGGGGCACGAAC | 254065 |
rs750279073 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731081 | TTTTAAAGCTTTTGA[C/T]ACATACTGCCAAATT | 254065 |
rs750280560 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80712599 | TGAGGAGCGTCTCTG[C/T]CTGGCTGCCCATCGT | 254065 |
rs750283567 | snp | C/T | 4.65257e-05 | 0.00482293 | synonymous-codon | BRWD3 | GRCh38.p7 | X:80676711 | AGGATCCTCAGTGGA[C/T]ACAAAATTGTCATTA | 254065 |
rs750286034 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80692582 | ACTAATATTCATAGC[C/T]ATATTCCAGCAATAA | 254065 |
rs750297827 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701688 | GAATTTCTAATAGCT[-/A]AAAATTTGAGCAGAA | 254065 |
rs750301885 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806873 | AGTCTAGTAAACTGG[A/G]TTGTTGGGGTTTTTT | 254065 |
rs750304399 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773652 | TACTCTTCCAGGGCA[C/T]AAATTCTCCACTTGA | 254065 |
rs750315499 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80725826 | ACATGCCTATATAAC[A/G]TAACATGTTTACATG | 254065 |
rs750318635 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726245 | TTTACATGTTATATG[C/T]CTGTATAACATATAA | 254065 |
rs750346415 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809891 | GTGGCGAAGAGGTGG[C/G]CGGGGGCAAAGGGGG | 254065 |
rs750347937 | snp | A/G | 0.000128816 | 0.00802443 | intron-variant | BRWD3 | GRCh38.p7 | X:80681520 | ATTTTAAAAGATTTT[A/G]ATACTAACATAATTA | 254065 |
rs750368538 | snp | C/T | 2.29761e-05 | 0.00338932 | intron-variant | BRWD3 | GRCh38.p7 | X:80681317 | AATAAATAATAAATG[C/T]CTTGTCCTGTATTTA | 254065 |
rs750369566 | snp | C/T | 2.28781e-05 | 0.00338209 | intron-variant | BRWD3 | GRCh38.p7 | X:80744257 | GTCATCTGAACCCTA[C/T]AGTAACAAAAGGACA | 254065 |
rs750392121 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753137 | ATTTGCAATTATTTT[C/G]TCCAATTCTACACAT | 254065 |
rs750400830 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785371 | TTTTTGCTCTTGCCA[A/T]AAGAAATCTAGAAAT | 254065 |
rs750405561 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732222 | AAAAATATCCACTTC[C/T]GGTATACCAAGCATT | 254065 |
rs750405619 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725455 | GCACTCTATTCTCTA[G/T]TACTGGTATTCAAAT | 254065 |
rs750431142 | snp | A/C | 2.33915e-05 | 0.00341983 | intron-variant | BRWD3 | GRCh38.p7 | X:80683973 | AGTAACTGGTTAAAG[A/C]AAACTGCCTGATAAT | 254065 |
rs750446858 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673209 | TACTCAGTTACTTTG[C/T]TACTTTGCATCTGCG | 254065 |
rs750451217 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80759763 | GGCTCAACATGATAG[C/T]TATAATTGGAGTGTG | 254065 |
rs750472832 | snp | C/T | 2.52465e-05 | 0.00355283 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728781 | GAAGCTGTCCTGTGA[C/T]AGAATTCCACACTTT | 254065 |
rs750504046 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693614 | AGTAAAGGTCACTCA[C/T]GCTATGCTATAATAA | 254065 |
rs750520733 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671750 | ATATACAATATCATA[C/T]CAACTATGAACTGAT | 254065 |
rs750536206 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80790451 | TCATGATCGAATTGC[C/T]TCTGTTCTAAAAGCT | 254065 |
rs750542482 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80801171 | TTGAGACCCAGCTAA[C/T]TATAAGACACAATGG | 254065 |
rs750558251 | in-del | -/CAA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737832 | ACAGCAAGACTGTCT[-/CAA]CAACAACATCAAAAG | 254065 |
rs750560939 | snp | C/G | 2.84224e-05 | 0.00376967 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793793 | AAAGTATAAATAAAA[C/G]ACAGGAAAAACACAT | 254065 |
rs750567754 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700733 | TAAGAGCAAAACTCC[C/T]TGTCAAAAAATAAAT | 254065 |
rs750572188 | in-del | -/AAATAAATAAATAAAT | 0.470238 | 0.118301 | intron-variant | BRWD3 | GRCh38.p7 | X:80788086 | GAGACTCTGTCTCAA[-/AAATAAATAAATAAAT]AAATAAATAAATAAA | 254065 |
rs750574689 | in-del | -/T | 5.2712e-05 | 0.00513354 | intron-variant | BRWD3 | GRCh38.p7 | X:80692069 | AAGAATTATAATTCA[-/T]TTTTTAAAAGCATAT | 254065 |
rs750580464 | in-del | -/TA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723228 | TGATATTAATGCAAT[-/TA]TATTGAGCTGACCTC | 254065 |
rs750583827 | in-del | -/AG | 2.44939e-05 | 0.00349948 | intron-variant | BRWD3 | GRCh38.p7 | X:80687018 | CCTACAGATTTTAAT[-/AG]AGTTATATCTAAAAG | 254065 |
rs750597553 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709978 | GAGCAGGATTCATCA[A/G]ACTGAATATGCAATG | 254065 |
rs750651058 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80741154 | TATGAGTGAGAACAT[A/G]CGGTGTTCGGTTTTT | 254065 |
rs750668930 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80760611 | CTTCAAAATTATTAT[A/G]TGAAATATTGTAACC | 254065 |
rs750669538 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729170 | CCAAAAACTACTAAG[A/T]AATCTATAAATACCT | 254065 |
rs750712883 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735325 | AAAGGAACGTGGTCA[A/G]TAAGTACTATTCTCA | 254065 |
rs750724252 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80717060 | TATTTCCAGTTGCTG[C/T]GGAGTATCTGAAAGT | 254065 |
rs750736620 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684292 | TGTGCCAACTACCTC[C/T]CCACAACCCCAAAAC | 254065 |
rs750737081 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80752965 | CCACCACGCCTGGCC[A/G]ATCATTTTTTTGTAT | 254065 |
rs750738870 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80750177 | CTTCAGAACATTGTT[C/T]TAGCCAATGATTTCT | 254065 |
rs750741848 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772672 | CAGAAATTAATAATA[A/G]AACTCTAAGAAACAA | 254065 |
rs750754866 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799564 | ACAGAACAGGCATAT[A/G]CAAAAGTTAGTCATG | 254065 |
rs750758596 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729595 | AATAGGGACAACTCT[A/C]AAGGTAGAAAGTAAA | 254065 |
rs750762726 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689734 | AAATAAGAGAAAAGT[A/C]ACTCATTCCTACTAA | 254065 |
rs750781917 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80705954 | CAAACACTACGCTTA[G/T]GTTACACTGAATTTA | 254065 |
rs750785429 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772061 | GGAAGACAGTGTGGC[A/G]ATTCCTAAACGATCT | 254065 |
rs750795211 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797201 | TGCATATTAACAACT[A/G]TAACAGCTTATTCCT | 254065 |
rs750818821 | snp | A/G | 2.30099e-05 | 0.00339182 | intron-variant | BRWD3 | GRCh38.p7 | X:80716276 | GTCAAAGGTCAAAGT[A/G]ACAGAAAATCAAGAA | 254065 |
rs750877876 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801505 | ACAGGCGTGAGCAAC[C/T]GCGCCCGGACGAGAA | 254065 |
rs750891756 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80734957 | GAAAAAAAAATCAAC[C/T]TTACACATTACTTAG | 254065 |
rs750902455 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80694944 | CATGAGATTTGGGAG[A/G]TGCCAGGGGCTGAAT | 254065 |
rs750923765 | snp | G/T | 2.2865e-05 | 0.00338112 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682572 | CTTATATTCAGAGAT[G/T]ATATTTTTGATATGA | 254065 |
rs750925337 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751101 | GGATACAAGGAAAGG[A/G]GAGGGGTGAGGAAAG | 254065 |
rs750933846 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80726213 | ACATGTTATATGTCT[A/G]TATAACATATAACAC | 254065 |
rs750946519 | in-del | -/AAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767769 | CAGAAGGTCAGTAAT[-/AAC]AAACTTCTCTGAGCT | 254065 |
rs750950325 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734296 | TTCCTTAGTTGTATG[C/T]TACCTTGCATTAGTA | 254065 |
rs750986809 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728009 | TGCAAAATAGAAGAA[A/C]TTTACATCCCTCTGA | 254065 |
rs750986832 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787768 | TGATAAATTAGACTT[C/T]AGCAAAAATTTCTGT | 254065 |
rs750989674 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80755326 | AAAAGATGATTTGGT[-/A]AAAAAAAAGTTAACA | 254065 |
rs750998577 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766141 | ATCCGGTGGGCTTTA[G/T]TCAATACCTTGGAGG | 254065 |
rs751020595 | in-del | -/AAA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736092 | TGATGGACAAAACTT[-/AAA]AAAAAAAAAATCTGA | 254065 |
rs751032359 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763640 | TCTATTTACGATCAC[A/G]CCAAAGAAAATGATA | 254065 |
rs751043981 | snp | A/G | 2.29053e-05 | 0.0033841 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719523 | TCTATTAACTGGTAA[A/G]TGTGGAACATCTCCT | 254065 |
rs751070072 | snp | A/G | 0.000114071 | 0.00755131 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734178 | CAAATAATATATTCT[A/G]ATCACATGGTCAGTA | 254065 |
rs751083890 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744258 | TCATCTGAACCCTAT[A/G]GTAACAAAAGGACAA | 254065 |
rs751088984 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706482 | TTTTTTTATTTTAAA[A/T]TTTTGTTTAAAAACT | 254065 |
rs751098940 | in-del | -/A | 0.196935 | 0.244303 | intron-variant | BRWD3 | GRCh38.p7 | X:80787573 | TAGACACCCATATGC[-/A]AAAAAAAAAAAAAAA | 254065 |
rs751107763 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80726053 | TTACATGTTATGTCT[A/G]TATAACACAACATGT | 254065 |
rs751115490 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80786730 | ATGTTAGCCAACCTG[G/T]TCTCAAACTCCTGAC | 254065 |
rs751121700 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797092 | CTAGTTTATAATTCA[C/T]ACCCTGCACATTCAG | 254065 |
rs751133098 | in-del | -/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80685031 | AACGTTCTAAATATA[-/T]CTTATTTTCTTAAAT | 254065 |
rs751141625 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762180 | GAGGCTCTCGGAAGT[A/T]GTTTACAAGCAAACA | 254065 |
rs751148198 | snp | A/G | 3.29576e-05 | 0.00405928 | intron-variant | BRWD3 | GRCh38.p7 | X:80744007 | TTTTACATATGTTCA[A/G]GCTAAATTTTATCAC | 254065 |
rs751169196 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802114 | TTAAATATTCTTTTT[C/T]TATAGTACTGTTTTA | 254065 |
rs751181994 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80696426 | AATCTTTAGGAAGAG[A/G]TTAGCATTTCCATTT | 254065 |
rs751184821 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80705792 | CAGTAAAAATATGAC[A/G]TAAAAGATTTTTAAA | 254065 |
rs751192224 | snp | C/T | 2.31693e-05 | 0.00340355 | synonymous-codon, intron-variant | BRWD3 | GRCh38.p7 | X:80684076 | AACATCCTTATAAAA[C/T]TCCAGAGGACTACCA | 254065 |
rs751198260 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80746406 | TTTTTTTTTCTTGTT[C/T]GCTTTGCCTTGTTCT | 254065 |
rs751227669 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779502 | GGAAGCAAAGCAGAT[C/T]GCTTGAGGTCAGAAG | 254065 |
rs751234197 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726194 | TATAACATATAACAC[A/G]TTTACATGTTATATG | 254065 |
rs751243464 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769827 | CTGGTTTTTTGACAA[G/T]ATCAACAAAACCGAT | 254065 |
rs751263772 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777605 | GGTCTCACCACGCTG[C/T]CCAGGCTAGTCTCGA | 254065 |
rs751265778 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710459 | CTAAATTTATGGAAT[A/G]CAATTTAAATGAACT | 254065 |
rs751279948 | snp | C/G | 2.33043e-05 | 0.00341345 | intron-variant | BRWD3 | GRCh38.p7 | X:80696716 | ACACACACTCAAACA[C/G]AGACTCAGAGATAAC | 254065 |
rs751284717 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712023 | AGAGTTTGACTCTTT[A/C]ATCAACAGCATTCTT | 254065 |
rs751311063 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792452 | GGTAACTGGTTATAA[A/C]TAGCTGTGTTTTTTT | 254065 |
rs751313444 | snp | C/T | 2.27996e-05 | 0.00337628 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722615 | TCTTTACAATTTTCC[C/T]GTCCTGGTACCAACC | 254065 |
rs751332926 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793906 | AATCAGGCCTGGGCG[C/T]GATGGCTCACGCCTG | 254065 |
rs751339060 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700994 | ACAACTGTACTATAC[C/T]TCAAATTATAACTGA | 254065 |
rs751356794 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738705 | CTGAGAGGGTGACAT[A/G]TGCACAAAGCACATA | 254065 |
rs751382352 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685772 | TGTTGAACACAATCT[A/C/T]GTTCCTTACTTGAAT | 254065 |
rs751383997 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773185 | GATACGCAAGTACTA[A/G]AAGTGTACAGAACTT | 254065 |
rs751385781 | snp | A/C | 2.30814e-05 | 0.00339708 | missense, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704728 | CTTCTAGGGACTTCA[A/C]ATTTTCCTCATCAGA | 254065 |
rs751388229 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769315 | CACCACAACACACCT[A/G]TTCCAAAATTGACCA | 254065 |
rs751389703 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80699890 | AACTGAGGGGAAAAA[A/T]CCATGGGTAAGCAAT | 254065 |
rs751405032 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80701632 | CATATTATGAGATTT[C/T]TAAAATACATTAACA | 254065 |
rs751415918 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755176 | CTTTTAGCTGTGCTG[C/T]TAGTTTACTTTTAAA | 254065 |
rs751422097 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778713 | TTTTATTTTTAAAAA[A/T]TTTGGCCAGGCACGG | 254065 |
rs751427582 | snp | A/G | 4.58085e-05 | 0.00478562 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677208 | ACTCTCCACTCTCTG[A/G]GGTGGATAAATGAGA | 254065 |
rs751433102 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711367 | GTTTTACTTAACCCT[A/G]TATAACGTGTTTTAA | 254065 |
rs751437369 | in-del | -/AAAG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730390 | AAATATTATTTAGCA[-/AAAG]AAAGAAAGAAAGAAA | 254065 |
rs751446058 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724105 | GCAAGGACATACCTC[A/G]TGAAATACTAAATGA | 254065 |
rs751447885 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746463 | CATAGCATAAGTCTA[A/C]ACAATTCTTCTCCAA | 254065 |
rs751479783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752456 | TGGACATTCTATTTT[C/T]AGTTCTTTGAGAAAT | 254065 |
rs751483771 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722317 | AGGTTTTCTAAAGAA[A/T]CAGGTCAATACATTA | 254065 |
rs751521189 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775397 | CAAGGGGCTTTACTT[-/G]ACACAATTGGGGCCC | 254065 |
rs751534954 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698211 | CTGGATATGATCTTA[A/C]AATAATCATACACAT | 254065 |
rs751538464 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730865 | ATTTCGTAGATCTAT[A/T]TCTATGTTTACAAGT | 254065 |
rs751546213 | snp | A/G | 6.84603e-05 | 0.00585025 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80693006 | TGCTGACTCTCCACA[A/G]TCCCAAACCACCAGG | 254065 |
rs751563601 | snp | C/T | 2.35059e-05 | 0.00342818 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80690033 | GGACTGTCTGGCTCA[C/T]TGAAAGTCCTGGCAT | 254065 |
rs751567425 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793876 | TATAGAGCAAAGTAC[A/C]GTTTTAAAATATGGA | 254065 |
rs751581469 | snp | C/T | 6.03637e-05 | 0.00549347 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791915 | GCCTCTATGCAGAGC[C/T]GCAAAAGCAGACCCA | 254065 |
rs751593169 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682978 | AATTTGTCCTAAGGA[A/G]ATATCACAGAATTAT | 254065 |
rs751596950 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744451 | AAAGCATTGTCCAAA[C/G]TGACAATGGCATTTG | 254065 |
rs751597272 | in-del | -/AT | 3.30049e-05 | 0.00406219 | intron-variant | BRWD3 | GRCh38.p7 | X:80685432 | AAGTAAAAACAATCA[-/AT]ATGTCTTTTAAGAGA | 254065 |
rs751598663 | snp | C/G | 4.69925e-05 | 0.00484706 | intron-variant | BRWD3 | GRCh38.p7 | X:80736112 | AAAAAAAATCTGATT[C/G]AAATAAAAAGTTTTC | 254065 |
rs751600360 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | BRWD3 | GRCh38.p7 | X:80735247 | CATGTTTGGCTAATG[A/G]GCCAGAATGTTAGCG | 254065 |
rs751605405 | snp | A/G | 2.36027e-05 | 0.00343523 | intron-variant | BRWD3 | GRCh38.p7 | X:80682119 | AAAATATGTAACAAC[A/G]AGCATTTTTTTTTTT | 254065 |
rs751622096 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715068 | TAAAAGTGTATGTAA[A/G]TGTTTCACATTTTCA | 254065 |
rs751623000 | snp | C/T | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670910 | TACACAGTATATATA[C/T]ATCAAAGATACAGTC | 254065 |
rs751630038 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709019 | AAAAATCAACATTCA[A/G]TGATCTCTATGAGGG | 254065 |
rs751656695 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789504 | CCTCAGCCTCCCCAG[C/T]AGCTGGGACTACAGG | 254065 |
rs751660111 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796627 | TTGGTAAGTTCCTTC[-/A]AAAAAAAAACAATTT | 254065 |
rs751681392 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80709870 | TAATAGTTTAGGCAG[A/C]AACTTCTTGATCCTC | 254065 |
rs751686089 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800453 | GCTGAGGTGGGAGGA[C/T]TGATTGAGCCCGGGA | 254065 |
rs751696887 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783681 | TAACCTAAGTATCCA[A/G]CACCAGACAACTAGA | 254065 |
rs751720757 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737960 | ACAGTCGCCTTACAC[C/T]GTCTATGGCTGCTTT | 254065 |
rs751722494 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80728368 | TTTCCTACTTCTTCC[C/T]CTTACCCCTATTCCT | 254065 |
rs751723732 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716617 | CTTCTTTTGCTTAGC[A/C]TGTTTATCCACGTTG | 254065 |
rs751729764 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80698942 | TTCTCAGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 254065 |
rs751738122 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685655 | TCATGTTTTATCGGC[G/T]GTACTTTAAGGTGAA | 254065 |
rs751750660 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674778 | TTTCTCTTAAAGCCT[A/G]AACATCATTTCCACT | 254065 |
rs751775718 | snp | G/T | 2.31871e-05 | 0.00340485 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80725036 | TGATCAAATGGATGG[G/T]CTTCTAGAACGAATA | 254065 |
rs751779741 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80790299 | GCTATAGAGAACTAT[A/G]ACCCACAAAGAGAAA | 254065 |
rs751793024 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736772 | TCATGTGGGCTTCTC[A/G]GGCTCTTACTCTCAG | 254065 |
rs751796528 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80749001 | AATTTGCATACATCT[A/G]TGAGCCTTCCAAGAT | 254065 |
rs751798037 | snp | A/G | 2.28198e-05 | 0.00337778 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677146 | GGAAGTTGATTCAGA[A/G]TCAGAGTCAGAACCA | 254065 |
rs751798241 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768432 | GCCAATATTCAACAT[G/T]CTTAAAGAAAAGAAT | 254065 |
rs751822843 | in-del | -/A/AA | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793160 | GCAAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 254065 |
rs751829058 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757805 | CATAAGATCAATAAA[C/T]AGCCATCAATGGACT | 254065 |
rs751857172 | in-del | -/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671611 | AACAAATTAGTCCAG[-/T]TTTTTTGTCTTTGAA | 254065 |
rs751862617 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80771282 | AACCAAAAAAGAGCC[C/T]GCAATGCCAAGACAA | 254065 |
rs751864583 | snp | A/C | 2.28311e-05 | 0.00337861 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734196 | CACATGGTCAGTACT[A/C]CCAGTTGTAATGAAC | 254065 |
rs751871533 | snp | C/T | 2.28739e-05 | 0.00338178 | missense, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793669 | ACACCTAATAATGTC[C/T]GTACCCCAGGAACAC | 254065 |
rs751872906 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767693 | AGGATTGCAGCTCCT[C/G]GCCAGCAACAGAACA | 254065 |
rs751900439 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758648 | TTCTACCCTTGGGAA[C/T]GACATTAAAAAAAGA | 254065 |
rs751907411 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80688426 | AGTGTTAGTATTTTT[A/T]AAAAACCTTATTCTA | 254065 |
rs751915224 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722138 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCAGTCTG | 254065 |
rs751920587 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749882 | CAGCATGATACTGAC[A/G]TAGAAACAGACACAT | 254065 |
rs751923950 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699861 | ATACACAATCAACAG[A/T]GAAATATGCATAAAA | 254065 |
rs751925765 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687610 | TTGGCATTTGAATGG[C/T]TTCCTAAATTATTAA | 254065 |
rs751949681 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80690670 | GGCTCCTTTCCTGTA[C/T]ATATTTCAGTGCTGG | 254065 |
rs751952639 | snp | C/T | 2.30319e-05 | 0.00339344 | intron-variant | BRWD3 | GRCh38.p7 | X:80733532 | TTCGTTAAAATGGAC[C/T]TATTTGTAAAATGAA | 254065 |
rs751954691 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726435 | CCTCATAAAGGAAAA[A/G]TTTACAAACATCTGC | 254065 |
rs751966120 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807759 | AAGTATATTCCATTT[G/T]TAAATATGTCCATTG | 254065 |
rs751992937 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741456 | GGTCAAATGGTATTT[C/G]TAGTTCCAAATGCAT | 254065 |
rs752032544 | in-del | -/C | 0.000125063 | 0.00790668 | intron-variant | BRWD3 | GRCh38.p7 | X:80809395 | AGCCTTCGCGCTAAG[-/C]CCCCATTCCCTTAGC | 254065 |
rs752034656 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766927 | ACTGTGCTTTCCCAA[C/T]GGTCTTAGCAAATGG | 254065 |
rs752035303 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80797063 | TATCATCTACAGAGT[G/T]ATATCCTAAAATCCT | 254065 |
rs752036755 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764739 | AAAGAATGAAAAGAC[-/A]AGACTAGGAGAAAAT | 254065 |
rs752055658 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704341 | TAAAAATGAGGACTC[A/G]AAATACCACATGACA | 254065 |
rs752073173 | snp | A/G | 2.34019e-05 | 0.00342059 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692144 | TTCTCTCTCATTATT[A/G]TCCCAGCTATTAAAA | 254065 |
rs752080843 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679064 | AGCCAGGGAAAAAGC[C/G]CTTATCAGATACCCA | 254065 |
rs752080850 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764051 | GAATAAAGGGCCAAA[A/C]AAATTTGCATAAATT | 254065 |
rs752093208 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80733378 | ATAAGGTATCTATCA[C/T]AGAAGTAGCTGCATC | 254065 |
rs752109548 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741123 | GTCCAGGTGTTCTCA[C/T]TGTTCAATTCCCACC | 254065 |
rs752118426 | snp | A/G | 2.29261e-05 | 0.00338563 | intron-variant | BRWD3 | GRCh38.p7 | X:80716260 | TGTACCCTAATAACA[A/G]GTCAAAGGTCAAAGT | 254065 |
rs752126453 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772018 | CTTTTACACTGTTGG[G/T]GGGAGTGTAAACTAG | 254065 |
rs752134496 | in-del | -/CTTG | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723124 | TGTAATTACATTTTT[-/CTTG]CTTATTTTTATTCAA | 254065 |
rs752145640 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80713400 | CCTTAACCCCAACCC[C/T]GTGCTCTCTGAAACA | 254065 |
rs752147862 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785840 | TGAGACCAGCCTAGC[A/C]AACATGGCAAAACCC | 254065 |
rs752173011 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693416 | TTCTTTAAAAATCTC[C/T]TCATACTAGTATTTA | 254065 |
rs752197919 | snp | C/T | 5.20888e-05 | 0.0051031 | intron-variant | BRWD3 | GRCh38.p7 | X:80689944 | TTAAGTTAGACTCTC[C/T]GGAAGCTAAAACTGC | 254065 |
rs752245192 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732843 | ACACTAAAGATTTCT[A/G]TAAAGAACAATGTTG | 254065 |
rs752247605 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795650 | CTTTGGGAGGCAAAG[A/G]TAGGAGAATCACTTG | 254065 |
rs752264694 | snp | A/T | 2.31492e-05 | 0.00340207 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719494 | AAATACTTACCACCA[A/T]TAACAGAGTATGCTC | 254065 |
rs752266015 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80806703 | GCTTGGTTCAAATCA[C/T]ATCGTACCTTAAATA | 254065 |
rs752266171 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80795129 | TAGATAAGAATGAAA[C/T]TATAAAACAACAAAA | 254065 |
rs752269232 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761473 | AAAAATTGTTAAATA[C/G]TGAGGAAAGGCAAAA | 254065 |
rs752272694 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776313 | TCATTATTTACATTA[C/G]AAAAAAAATATGTTT | 254065 |
rs752276969 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727615 | TAACAATAAAATATC[A/T]GATAGTGATAAACCT | 254065 |
rs752284087 | snp | G/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669860 | ATTTACTTACAAAAC[G/T]TATAAAATTGAAGAG | 254065 |
rs752289725 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810636 | AAGAGTTTTCAATAA[C/T]CTTTATGTATTATTG | 254065 |
rs752303484 | in-del | -/AAAG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768795 | ACTGGCAAATTGTAT[-/AAAG]AGTCAAGACCAATCA | 254065 |
rs752307911 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678469 | CAAGACAAGACATTT[A/T]TTTAAAAAAAAGAAA | 254065 |
rs752313217 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80713370 | CTTCTGCCTTGGGAT[C/G]CTGTTGATCTATGAC | 254065 |
rs752345055 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80705602 | ACAGAGTATACTTAC[A/G]CAAACCTAGACAGTA | 254065 |
rs752364356 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755085 | ATTATGGTTTCTTCC[-/T]TGATTCTGTTTATGT | 254065 |
rs752365475 | snp | A/G | 2.9742e-05 | 0.00385618 | intron-variant | BRWD3 | GRCh38.p7 | X:80695881 | TACATAAGCTTAATA[A/G]TTATTAAACAACAAT | 254065 |
rs752371717 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733269 | AGGACGACCTGATAG[G/T]CTATGGTTACTACTT | 254065 |
rs752374748 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777488 | GCCTCAACCTCCTTG[C/G]CTCAAGTGATCCTAC | 254065 |
rs752378402 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799273 | CTGGGCACTGAATAA[A/T]ATGTAAAAGGTAGCA | 254065 |
rs752398099 | snp | C/T | 2.28321e-05 | 0.00337869 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677162 | TCAGAGTCAGAACCA[C/T]AGGTACTTTCAGAAC | 254065 |
rs752433241 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768628 | CCACTGCAAAAACAT[A/G]CCAAATTGTAAAGAC | 254065 |
rs752434666 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729236 | AAAATATGAAAACAT[A/G]ATGGCCAATTTATTA | 254065 |
rs752437707 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706394 | GATTACAGAAGTGAG[C/G]CACCACGTTCGGCAA | 254065 |
rs752447196 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786529 | GCCTATATATATATA[A/T]ATATGGAGTCTTGCT | 254065 |
rs752451200 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764617 | CGCGCCCAGCCTTAG[C/G]CAAAGAATTCTTAAA | 254065 |
rs752455416 | snp | A/G | 2.2811e-05 | 0.00337713 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717659 | CATCTGGCTCCGAGG[A/G]GCATTGTTATGCATT | 254065 |
rs752460463 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80743987 | AATCAGAGAATTCTC[A/G]CCTTTTTTACATATG | 254065 |
rs752472510 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788798 | ACACATGAAATGACA[C/T]GCATGAATTTCAAAA | 254065 |
rs752493456 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712917 | CCTCCGCCCGGCAGC[C/T]GCCCCGTCTGAGAAG | 254065 |
rs752516871 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722137 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCAGTCT | 254065 |
rs752542967 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694611 | ACCTCTTGCATCAGC[A/G]TGACCTGGATATGAG | 254065 |
rs752544574 | snp | A/G | 2.29732e-05 | 0.00338911 | intron-variant | BRWD3 | GRCh38.p7 | X:80688142 | TTAATTAAAAAGGAA[A/G]AGTGGGAAAAGACGT | 254065 |
rs752551941 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80683519 | GCAACTGATTAAAAG[C/G]TAATCAGATACCAGT | 254065 |
rs752571831 | snp | A/T | 2.98891e-05 | 0.0038657 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791861 | TTACTCACCCACATT[A/T]GGAGGTTTCACATAA | 254065 |
rs752573256 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80729336 | AATTAAATATGACAT[C/T]ATCAATGGGCGACTA | 254065 |
rs752578912 | in-del | -/GTTTT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778697 | ACCTGGTCAACATTA[-/GTTTT]ATTTTTAAAAAATTT | 254065 |
rs752596466 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80791004 | ACTTCAGAGTATCCA[A/G]TTTCCCTGAATAAGT | 254065 |
rs752596914 | snp | A/C | 0.000242885 | 0.0110174 | intron-variant | BRWD3 | GRCh38.p7 | X:80707420 | AAATTAAAACCATTA[A/C]AACTACCTGGAAGAA | 254065 |
rs752607959 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719077 | TTTTTTTTTTTATTC[A/G]AGAGAAGAGCATGGT | 254065 |
rs752608842 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80760886 | AATTTACTATCCTGA[C/G]TTAAAAGCTTAGTAC | 254065 |
rs752611796 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80683038 | AAGATATTACCTATA[A/G]CATTATTCATGTAAA | 254065 |
rs752625902 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711199 | TAAGTGGATTTAATA[A/G]TCTATACTTTTGTTC | 254065 |
rs752668699 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790194 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 254065 |
rs752676430 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720892 | GTACCATTGTATGTA[C/T]AACTGTCTATGGTAT | 254065 |
rs752679874 | in-del | -/GGGGGGT/GGGGGTG | 0.00528622 | 0.0511715 | intron-variant | BRWD3 | GRCh38.p7 | X:80738624 | TGTGCACACAGTGGA[-/GGGGGGT/GGGGGTG]GGGGGTGGGGGGGGC | 254065 |
rs752683129 | in-del | -/AAAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720553 | AGTCGAAAAGTTAAA[-/AAAC]AAACAAACAAACAAA | 254065 |
rs752686686 | snp | C/T | 6.9752e-05 | 0.00590518 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704714 | TTTCTTCTGCCTTTC[C/T]TCTAGGGACTTCAAA | 254065 |
rs752695706 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674427 | TCAACAAAAAATTTC[A/C]AACTAAAATGATACA | 254065 |
rs752696912 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769230 | CTGAACTCAGCTCTG[A/C]AACAAGCAGACCTAA | 254065 |
rs752715216 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802025 | TTACACTAAATATCT[C/T]TTGACATACATTCAT | 254065 |
rs752737920 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753066 | TTGTTTCTGAGTTTT[G/T]TTGTTGAGTTGAGTT | 254065 |
rs752762754 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773778 | GGTCATTTATTCCTT[C/G]AAGTCTTCCCATGTT | 254065 |
rs752769311 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714411 | TACCCAAACCCTTAT[C/T]TTAATCCAGACATTC | 254065 |
rs752784355 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742796 | TAAGGAGATTTTGGG[A/C]TGAGACGATGGAGTT | 254065 |
rs752788404 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80798392 | ACTCTTACCCCGAAT[A/G]GTTTTTTTTTTACAT | 254065 |
rs752810246 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799429 | TATAGCAGAGAATAC[A/G]CTATTTGTTTTCCAA | 254065 |
rs752830036 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80691292 | ACTTTTCTAAAACCA[A/T]GAGGATTCCATTATA | 254065 |
rs752832222 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757531 | TGAGAAAAACAATTC[C/T]TTAGCAATGTTGAAT | 254065 |
rs752838836 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80709769 | TTGATCACTCTCCTA[-/T]TTTTGTAAACCTTGT | 254065 |
rs752838886 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80757917 | TATAAACAAGTCAAA[C/T]AGGCTGGGCGCGGTG | 254065 |
rs752840206 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804114 | TATTTTGCATATAAA[A/G]TGAGGGTAATACAAT | 254065 |
rs752851555 | snp | G/T | 3.44839e-05 | 0.0041522 | intron-variant | BRWD3 | GRCh38.p7 | X:80709602 | AGAAGAATAATAAAT[G/T]TTAAAAAAGGAAAAG | 254065 |
rs752852770 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772992 | GAAAGTTACATAGTG[C/T]ATAATTCCATTGATA | 254065 |
rs752870006 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80725210 | GACATGGATACTACA[A/T]GAACAATATAGGTCA | 254065 |
rs752878397 | snp | C/T | 0.000329245 | 0.0128263 | intron-variant | BRWD3 | GRCh38.p7 | X:80809224 | ATTCACCACGACTCC[C/T]AGATCTCTTTCTTCC | 254065 |
rs752898370 | snp | A/G | 3.24323e-05 | 0.00402679 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745714 | CCGGTTAATTGCCTG[A/G]CAGAGGTGATATTCA | 254065 |
rs752906746 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697894 | TCCAGATTGCTTTCC[A/G]CAGTGGCTGAACTAA | 254065 |
rs752925015 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80699204 | TGGGCAACAGAGCGA[A/G]ACTCCGTTGCAAAAT | 254065 |
rs752929319 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753415 | GCTGGGATTACAGGC[A/G]GCTGCCACCACGTCT | 254065 |
rs752940414 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771705 | ATAGGAGAAAATTTT[C/T]GCAACCTACCCATCT | 254065 |
rs752945348 | in-del | -/A | 2.33593e-05 | 0.00341747 | intron-variant | BRWD3 | GRCh38.p7 | X:80808636 | GGGGGAAGCGGAGGC[-/A]AATGATGAAGGAAAA | 254065 |
rs752951345 | snp | G/T | 2.53501e-05 | 0.00356012 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685480 | AGAAAGAGATGAATC[G/T]TGTTGTCTTTCTGGA | 254065 |
rs752978608 | snp | C/T | 0.000628262 | 0.0177129 | intron-variant | BRWD3 | GRCh38.p7 | X:80735234 | TTTTGTGTTTCATCA[C/T]GTTTGGCTAATGGGC | 254065 |
rs752994487 | snp | A/C | 2.31551e-05 | 0.0034025 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80729972 | TTCTTGTTGCTGATA[A/C]TGCCAAATTCTTGCC | 254065 |
rs753027445 | snp | G/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672542 | ACTTAATTTTATATT[G/T]CAATTTAATCAAAAC | 254065 |
rs753042594 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780321 | ATGTTCATACTAGGA[C/T]TAAATGGAGAAAATA | 254065 |
rs753050311 | snp | C/G | 5.86012e-05 | 0.00541269 | intron-variant | BRWD3 | GRCh38.p7 | X:80809313 | TACAGCTCTGGGGAA[C/G]AGGGGGGAAAAGAGG | 254065 |
rs753050467 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789969 | GGATCACTTGAGGCC[A/G]GGAGTTCAAGACCAG | 254065 |
rs753062041 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765644 | TGTATAAAACAGTTT[A/C]TTTGCTTTCCTTTAT | 254065 |
rs753062288 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80758488 | GGCAGATGGCCATTC[C/T]GACCTCTGCCTAAAC | 254065 |
rs753068669 | snp | C/G | 5.69363e-05 | 0.00533525 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809021 | TCCGTACCTGATGCT[C/G]CTCGAGCTCCTGCAC | 254065 |
rs753068953 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789447 | GTGGCGCGATCTCGG[C/T]TCACTGCAAGCTCCG | 254065 |
rs753128855 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747319 | ATTCTTTGCTGTGGG[A/G]ACTTTCCATTGCAGG | 254065 |
rs753132073 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80708771 | CAGTGAGCCAAGTAC[A/G]TGTCACTGCACTCCA | 254065 |
rs753135176 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749852 | AAATGTATGATAAAG[C/T]TTATTTAATAGAAAC | 254065 |
rs753172652 | in-del | -/T | 6.36862e-05 | 0.00564261 | splice-acceptor-variant | BRWD3 | GRCh38.p7 | X:80736090 | GTTGATGGACAAAAC[-/T]TAAAAAAAAAAAAAT | 254065 |
rs753182865 | snp | C/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80712680 | AGCGTCTCTGCCCAG[C/G]CGCCATCCCATCTAG | 254065 |
rs753185655 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711346 | CGACAAAGTCTCATC[A/C]GAGGGGTTTTACTTA | 254065 |
rs753187834 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80721894 | CTCTGTCGCCCAGTC[G/T]GGAGTGCAGTGGCGC | 254065 |
rs753193604 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740698 | AGGCTGCAGTGAGCC[A/G]AGATCCCACCACTGC | 254065 |
rs753212429 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805368 | TATACATATGAACAA[A/G]AAGGCAGGATTTTTG | 254065 |
rs753221837 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781962 | ATTCAACGCAATCCC[A/G]ATCAAAATACCAATG | 254065 |
rs753232007 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734837 | GAATTTTTGTGTTGA[C/T]TGCGGGGCAGTAAAC | 254065 |
rs753238633 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781303 | CCGTGTGCTCTCAGG[C/T]GATAGATGAGTGGCT | 254065 |
rs753255814 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794168 | GGGCAACACAGCGAG[A/G]CTCTGACTCAAAAAA | 254065 |
rs753256291 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | BRWD3 | GRCh38.p7 | X:80748691 | ACAAACCAACTTTAA[A/G]ATTTGTTAATCTTTT | 254065 |
rs753279742 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721220 | TGGTTTTCATCTTGT[C/T]CTCTAGTCAGATTTG | 254065 |
rs753284829 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714832 | TGCGGACAATATAGA[A/G]GAAGAGAAATTGAGT | 254065 |
rs753285097 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770649 | CAGCCAATATCATAC[C/T]GAATGGGCAAAAACT | 254065 |
rs753321851 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796651 | ACAATTTGAATCTAC[C/G]AAAATAATTGAAGCC | 254065 |
rs753342304 | snp | A/G | 2.6482e-05 | 0.00363872 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704672 | ATAACTTATAAAGTT[A/G]CAAACCTTCTTTCTA | 254065 |
rs753344831 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770592 | AACTAGGTACTGATC[A/G]AACGTATTTCAAAAC | 254065 |
rs753345797 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720900 | GTATGTATAACTGTC[C/T]ATGGTATTCAGTGCA | 254065 |
rs753356696 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80805137 | AAACACTAAACACTA[A/C]ATCAGATGACCGTTT | 254065 |
rs753373070 | snp | C/T | 2.35735e-05 | 0.0034331 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809499 | GGGGTTTGGGGGCTT[C/T]GCTCCGGAGGGGCTG | 254065 |
rs753382378 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769622 | CTTACAGCACTAAAT[-/G]GCCCCTAACAGAAAG | 254065 |
rs753387965 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80687382 | AGAACACTTGAATGA[-/T]TTTTTTTTCCCAGAA | 254065 |
rs753408082 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686624 | TGAAATAAAAGTCGG[A/C]AAGAACAGCAAATGA | 254065 |
rs753418781 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693269 | AATAAATTACATATG[A/G]CCACATCTTAAATAA | 254065 |
rs753433679 | in-del | -/AC | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669571 | TTCAAATGATCTATT[-/AC]ACAATTTGTTATGCA | 254065 |
rs753437144 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703117 | TTCTATCAGGTTGAA[C/T]GTGTTTTGTTTTTTT | 254065 |
rs753449963 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731332 | ACAATAATGTATTTT[A/C]TCCTTAATGGAAAAA | 254065 |
rs753479341 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794751 | TCATTTGCTTAGCTG[C/T]TAATCTTATGAAATA | 254065 |
rs753479366 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713162 | GTGAGGAGCCCCTCT[A/G]CCCGGCCACCACCCC | 254065 |
rs753502801 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80740584 | AATCCCTGTCTCTAC[-/A]AAAAAAATACAAAAT | 254065 |
rs753539891 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798475 | TATTATAAACCACTC[-/T]TTTTGTTTAAAGCTC | 254065 |
rs753541037 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748494 | AAATGTTTGGTAGAA[C/T]TCAACAGAAAAGCCA | 254065 |
rs753568761 | snp | A/G | 0.00015152 | 0.0087027 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745701 | AAAGCGACTACAGCC[A/G]GTTAATTGCCTGGCA | 254065 |
rs753573741 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678370 | TGGGTGAATGGTAGA[A/G]ATATTTTGCCAAGGT | 254065 |
rs753590279 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726362 | GTATAACATATAACA[C/T]GTTTACATGTTATAT | 254065 |
rs753596744 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771156 | CGAAGAATCAGTATC[A/G]TGAAAATGGCCCTAC | 254065 |
rs753617622 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80775286 | GAATAATTGGGCCCC[-/T]ACCTCCCTTTCCAGT | 254065 |
rs753626971 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810462 | AAATGCTCCTGGATT[C/T]TGACAAATATTGCAT | 254065 |
rs753632145 | in-del | -/TTTG | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80692730 | GTGTTTAGTTATTCC[-/TTTG]TTTTAGTCAAAGAAA | 254065 |
rs753636133 | in-del | -/AA | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80785619 | TTATTGTTTTTGGCC[-/AA]AGTCTGTTGTAAAAC | 254065 |
rs753657923 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706203 | AATCTCTGCCTTCTG[A/G]GTTCAAGAAATTCTC | 254065 |
rs753663512 | snp | A/G | 2.3182e-05 | 0.00340447 | intron-variant | BRWD3 | GRCh38.p7 | X:80744277 | ACAAAAGGACAATAG[A/G]TTTATAATGAAGCAG | 254065 |
rs753675426 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740549 | TCCAGGACTTTGAGA[C/T]CAGCCTAGGCAACAT | 254065 |
rs753718562 | in-del | -/GT | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80725860 | ACATGCCTATATAAC[-/GT]ATAACATGTTTACAT | 254065 |
rs753721716 | snp | C/T | 4.57268e-05 | 0.00478135 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682076 | CTGCAACTTCATTTG[C/T]TTCTGCTTCCCTTTT | 254065 |
rs753741393 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777480 | TCACTGCAGCCTCAA[C/T]CTCCTTGGCTCAAGT | 254065 |
rs753741546 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759272 | CTGTCTAAAATTTTG[C/T]CTGGGGTTAAAGCTG | 254065 |
rs753746923 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791950 | ATAGTGTACTCTTAC[A/G]GTCTATATAAAAAGA | 254065 |
rs753754305 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80683309 | AACTGTAAGTAAAAA[C/T]AGGTGATAGGTTTCA | 254065 |
rs753759941 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80736971 | CTAAGGATTAAGATA[C/T]ATAGGGTTTGAATAC | 254065 |
rs753767050 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709184 | TTTTCACTGTCTCAA[C/T]GTCAAACTCTTGCTG | 254065 |
rs753780561 | snp | C/T | 2.31833e-05 | 0.00340457 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723758 | CTAACCTTTTCGTAG[C/T]ATTTACTGCATCCAA | 254065 |
rs753781215 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80800495 | CAGTGAGCCATGATC[A/G]AGCCACTGCACTCCA | 254065 |
rs753783738 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679814 | GGTGGTCGGGACAGA[C/T]ACCGTACTATAAAGG | 254065 |
rs753789628 | snp | C/T | 2.30875e-05 | 0.00339753 | intron-variant | BRWD3 | GRCh38.p7 | X:80733447 | CACAAATATGTATTA[C/T]ATAATTACCTGTCTC | 254065 |
rs753801203 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745424 | TATAAAATGAGAAAC[-/T]TTTTTTCAATTTCCA | 254065 |
rs753808386 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725994 | ATATGTCTATATAAC[-/AT]AACATGTTTACATGT | 254065 |
rs753817118 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776803 | ACTGTCCTTGCTTCA[C/T]GATGGTACCCGATCC | 254065 |
rs753855395 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716692 | GCCATTTTGTACATA[C/T]ACCACAATTTGTTTA | 254065 |
rs753872454 | in-del | -/A | 0.0031746 | 0.0397142 | intron-variant | BRWD3 | GRCh38.p7 | X:80762070 | AAAAATGCAAGAGAC[-/A]AAAAAATACAGCTGA | 254065 |
rs753890850 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808303 | ATCCACAACACGGCA[-/C]CTCTGATAATCAACT | 254065 |
rs753907276 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751179 | CAAGTTTTGAGATTT[A/T]CTGTACTACATGGTG | 254065 |
rs753914523 | snp | C/T | 7.57748e-05 | 0.00615481 | intron-variant | BRWD3 | GRCh38.p7 | X:80709399 | GGAAACAAAAAACTA[C/T]ATCAAATAAATAATA | 254065 |
rs753936085 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80690384 | TCAAAAGAATGTTTA[G/T]TTTAGTTTTCAGGGG | 254065 |
rs753949632 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701614 | GAAAGTAACAAAAAA[A/T]ACCATATTATGAGAT | 254065 |
rs753953065 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792408 | CTTGCCAGTTGTGTC[A/G]TAACAGATAACAGCA | 254065 |
rs753971316 | snp | C/T | 4.97061e-05 | 0.00498504 | intron-variant | BRWD3 | GRCh38.p7 | X:80729896 | TGAGAACCACATAAA[C/T]ATCTAACATATATTC | 254065 |
rs754001960 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | BRWD3 | GRCh38.p7 | X:80714193 | TCATCTGCATAATAA[A/G]AATCTTGGTCTTCAC | 254065 |
rs754024739 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776322 | ACATTAGAAAAAAAA[-/T]ATGTTTGTATTACAA | 254065 |
rs754043968 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721989 | GTAGTTGGGATTACA[A/G]CCGTGCACCAACACC | 254065 |
rs754057467 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680197 | ACAAACTTCAAATAG[C/G]TGAACATGTTAGAAC | 254065 |
rs754078647 | snp | C/T | 6.86593e-05 | 0.00585875 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691077 | CGATTTTCAAGTCTC[C/T]GCCTGATGGTATTGA | 254065 |
rs754079205 | in-del | -/A | 0.000161435 | 0.00898285 | intron-variant | BRWD3 | GRCh38.p7 | X:80733450 | AAATATGTATTACAT[-/A]ATTACCTGTCTCCAT | 254065 |
rs754080374 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720048 | TTGTGGTGTTATTGG[A/C]ATAAACAAACCTACT | 254065 |
rs754080517 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803899 | GAATACAGGTATGTC[C/T]GGAATTTAAATACAG | 254065 |
rs754084875 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756906 | ATGTCTCTATCAAAT[A/G]CCACTGAGTGAACTG | 254065 |
rs754087199 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788499 | AGAAGATGGTGAGAA[C/T]GTGGGACAACTAGAA | 254065 |
rs754090837 | snp | A/T | 2.33103e-05 | 0.00341388 | intron-variant | BRWD3 | GRCh38.p7 | X:80696703 | TAGGTATTAAAATAC[A/T]CACACTCAAACAGAG | 254065 |
rs754093398 | snp | C/T | 2.31179e-05 | 0.00339977 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691861 | CCCTGAATAACCCGT[C/T]CACATTCTTCGTCTC | 254065 |
rs754096739 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741874 | TTGCCTGTTCACTCT[A/G]ATGGTGGTTTCTTTT | 254065 |
rs754127701 | snp | C/T | 6.99488e-05 | 0.0059135 | intron-variant | BRWD3 | GRCh38.p7 | X:80696688 | CTCTAAAATATACAA[C/T]AGGTATTAAAATACA | 254065 |
rs754138035 | snp | A/G | 2.58816e-05 | 0.00359724 | intron-variant | BRWD3 | GRCh38.p7 | X:80808492 | GTACAAGGTGGGGAG[A/G]GAGTGGTGAAAGAGT | 254065 |
rs754155037 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695223 | GTCCTAAGGCCTCCC[A/G]AGCCATGTGGAAATG | 254065 |
rs754156762 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772903 | CCACAGAATATCACT[C/G]AGCAATGAAAAGGAA | 254065 |
rs754163796 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779693 | CTTGAAAGAAGCCAC[A/G]AAAGCGACAAAAATG | 254065 |
rs754178843 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766401 | CTTATAATAAATACA[C/T]CTATCAATCCTACTG | 254065 |
rs754200994 | snp | A/T | 2.70256e-05 | 0.00367587 | intron-variant | BRWD3 | GRCh38.p7 | X:80707537 | AATTAAGATATATGG[A/T]TATTACCAGCTAATG | 254065 |
rs754211361 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80680954 | GTATGAGTTGTATGC[C/T]ACCACATGTGGCTAC | 254065 |
rs754214349 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798257 | TATATCGATGTAGTT[C/G]TTAAAATGTTTCTTC | 254065 |
rs754221591 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706819 | ACGACTGCTTGAGCC[C/T]AGGAGTTCAAGGCAT | 254065 |
rs754227470 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788570 | ACTTTCACAACAGTT[C/T]GGCAGTTTCTTATAA | 254065 |
rs754267603 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80715291 | AACAATAAAAGTTAA[A/G]AAAGCAAACATCAAA | 254065 |
rs754279610 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773615 | GATAGGCACTCAGGT[A/G]TTAACATCCAACCAT | 254065 |
rs754298107 | snp | C/T | 0.000257575 | 0.0113455 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735192 | GTAAATTTCACCGGG[C/T]GATCTCTAAAGATAA | 254065 |
rs754302839 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80720542 | TACTACAAAAGAGTC[A/G]AAAAGTTAAAAAACA | 254065 |
rs754312125 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763854 | CCTTTCAAAAGGCTT[C/T]TGTAGACATCAAGGA | 254065 |
rs754320625 | snp | A/C | 2.65322e-05 | 0.00364217 | intron-variant | BRWD3 | GRCh38.p7 | X:80685457 | TAAGAGACTACCAGG[A/C]CTACCTCAGAAAGAG | 254065 |
rs754332417 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727283 | GTGACCAGAATTAAA[A/G]GGTATTTTTCAAAAG | 254065 |
rs754362342 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754744 | GGGCATGGTGGCTCA[C/T]GCCTATTATCCCAGC | 254065 |
rs754378013 | in-del | -/AACATATAACAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726217 | GTTATATGTCTGTAT[-/AACATATAACAC]GTTTACATGTTATAT | 254065 |
rs754388488 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789439 | GGAGTGCAGTGGCGC[A/G]ATCTCGGTTCACTGC | 254065 |
rs754388923 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801589 | CTCACACCTGTAATC[C/T]CAACATTTTGGGAGG | 254065 |
rs754394440 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732722 | CTGGATCTAAGGATT[C/G]ATATAGAGAATAGTA | 254065 |
rs754396311 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80709713 | AAAATAAAGTCAACA[C/T]AGAACTATATTTATA | 254065 |
rs754406971 | snp | A/G | 2.31174e-05 | 0.00339973 | synonymous-codon, intron-variant | BRWD3 | GRCh38.p7 | X:80684031 | CTTTTTATTAGAGGT[A/G]TAAGCTTTGGAGTTG | 254065 |
rs754413924 | in-del | -/AGAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702359 | AGAAAAATAGTCCTT[-/AGAC]AGGAGTCTCATTAGG | 254065 |
rs754418674 | snp | C/G | 0.01368 | 0.0815649 | intron-variant | BRWD3 | GRCh38.p7 | X:80735678 | GCATAGTGGCGGGTG[C/G]CTGTAGTCCCAGCTG | 254065 |
rs754419270 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778960 | GCCAAGATGGTGCCA[C/T]TGCACTCCAGCCAGG | 254065 |
rs754422276 | snp | A/G | 2.33326e-05 | 0.00341552 | intron-variant | BRWD3 | GRCh38.p7 | X:80734256 | AAAACATAGTACCAA[A/G]GAACCTTAAAAACCC | 254065 |
rs754422423 | in-del | -/AAAGG | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726426 | GTTTATATGCCTCAT[-/AAAGG]AAAAGTTTACAAACA | 254065 |
rs754438394 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775845 | TAATTACAAATTATA[C/T]TTTCATAACATTTTA | 254065 |
rs754446297 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80731397 | GAAAGAACAGTAGCT[A/C]TACTAATGTTCAAGC | 254065 |
rs754468733 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80712677 | AGGAGCGTCTCTGCC[C/T]AGCCGCCATCCCATC | 254065 |
rs754478178 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758068 | GCCAGGCGTGATGGC[A/G]CATGACTGTAATCCC | 254065 |
rs754503920 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678626 | AGTAAGTAAAGAGAG[A/G]CAACGTGGCTGAAGA | 254065 |
rs754507100 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739560 | TACAATATGTAAAAG[A/T]AATGAGAAAATAAAC | 254065 |
rs754508472 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763281 | AAACCCAGGCAATCT[C/T]GTTTCAAAGGCTGAT | 254065 |
rs754527827 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759393 | TGGTTTCACAAAGAA[C/T]ATCTTCCAGTGAAAA | 254065 |
rs754531422 | snp | C/T | 2.3601e-05 | 0.00343511 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686996 | TGTCTTCTGCCTCGG[C/T]ATTTGACCTACAGAT | 254065 |
rs754533003 | snp | G/T | 8.69855e-05 | 0.00659433 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80676584 | GGCCATTGAATTTTT[G/T]AAGTTATTCTAAATT | 254065 |
rs754540559 | snp | A/G | 2.3067e-05 | 0.00339602 | intron-variant | BRWD3 | GRCh38.p7 | X:80716288 | AGTAACAGAAAATCA[A/G]GAAGAAAACCAATCA | 254065 |
rs754558865 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725894 | TTACATGCCTATATA[A/G]CATGTTTACATATGT | 254065 |
rs754578248 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770610 | CGTATTTCAAAACAA[C/T]ACAAGCTACTTATGA | 254065 |
rs754584054 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805196 | ATATGTAATTTAGTA[C/T]AAACACTGAATCAGA | 254065 |
rs754585471 | snp | C/T | 0.00791544 | 0.0624105 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810016 | CCGGAGCCCGATGGT[C/T]GCTTAGCTACAGCTC | 254065 |
rs754589982 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706310 | GACAGGGTTTTACCA[C/T]GTTGGCCAGGCTGGT | 254065 |
rs754594513 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762490 | TTAATGGATCTAAAG[C/T]GGTGAACTCCTCCTC | 254065 |
rs754599845 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796740 | TCCAGGGTTTAGCAT[C/T]AGGACAGAGGATTAA | 254065 |
rs754618036 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795055 | GTAGCCAAAATTCCT[C/T]GAAACAAAAACTTGT | 254065 |
rs754619119 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80794552 | ATATCTCTATATGTA[C/T]GTGTATAGATATATA | 254065 |
rs754629021 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80753294 | TTTTTTTTTTTAGAT[G/T]GAGTTTCACTCGTCA | 254065 |
rs754629119 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747244 | GTAGATGCAGGGGAG[-/A]AAGGTTACTTTAAGG | 254065 |
rs754636120 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703118 | TCTATCAGGTTGAAC[A/G]TGTTTTGTTTTTTTT | 254065 |
rs754710367 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703442 | AAGTTAGTGCTCTTG[A/G]GGCTCCACAGAAAAA | 254065 |
rs754713917 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740571 | AGGCAACATGTCGAA[C/T]CCCTGTCTCTACAAA | 254065 |
rs754719700 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725680 | ATGCCTATATAACAT[A/G]TAACATGTTTACATG | 254065 |
rs754722545 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736232 | TTCAAGGGACTATTT[A/G]ACTTTCCTAGATTAA | 254065 |
rs754741013 | snp | C/T | 2.32097e-05 | 0.00340651 | intron-variant | BRWD3 | GRCh38.p7 | X:80681959 | AATATCAGAATTAAA[C/T]CGAGATGCAGAACAC | 254065 |
rs754743041 | in-del | -/CACG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750894 | ACACACACACACACG[-/CACG]CAAAAATCATTAAGT | 254065 |
rs754746250 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80717854 | GTAGATTCAAATATA[A/G]TACTGCTGTAAGAAT | 254065 |
rs754748465 | snp | A/C | 2.30237e-05 | 0.00339283 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723787 | AAAACCAAAAAGCAG[A/C]AAATGTCCATGAGAA | 254065 |
rs754748786 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767946 | ATGCAGAAGCTTCAA[C/T]AGCCGATTCGATCAA | 254065 |
rs754750239 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810295 | ACCCCGTGGAAAGGC[G/T]GCTAGCTGGCTAAAG | 254065 |
rs754793913 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720115 | TATGCACAGTACATA[A/G]TATTTGGTAATAAAT | 254065 |
rs754799062 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744694 | AATGATAATTTCTGG[G/T]AAAAATATATTAAAC | 254065 |
rs754811780 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80693776 | GAGCATTCAGTTTTA[C/T]GTATTCACAAAGATG | 254065 |
rs754836438 | snp | G/T | 4.55981e-05 | 0.00477462 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722722 | GGTTTGTTCATCCAA[G/T]ACATAGTTATTGGCA | 254065 |
rs754870363 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799722 | TTACTAGCTGTTACT[A/C]TTTTTTGGCAGTATG | 254065 |
rs754871105 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768531 | AGACAAGCAAACGCT[A/G]AGAGATTTTGTCACC | 254065 |
rs754892510 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807240 | TCTCCATCTGAGAAA[C/T]TGTTACTATTAATAA | 254065 |
rs754904728 | snp | A/G | 6.75379e-05 | 0.00581071 | intron-variant | BRWD3 | GRCh38.p7 | X:80809337 | AAAGAGGTTCAGAGG[A/G]AGGTAGAGAAGAGAA | 254065 |
rs754909352 | snp | C/T | 3.93205e-05 | 0.00443382 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703591 | AGAAACCAGTCCTCC[C/T]TTCTAAAACATAAAT | 254065 |
rs754914746 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671082 | CACTGAATTAAAGCA[C/T]CATTTACAATGTAGG | 254065 |
rs754945562 | in-del | -/A | 0.0660089 | 0.169255 | intron-variant | BRWD3 | GRCh38.p7 | X:80800540 | GTGAGATGCTGTCTC[-/A]AAAAAAAAAAAAATA | 254065 |
rs754952880 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80710075 | TTGAAAAGGGCACCA[C/T]CGGAGCTTGCAGCTC | 254065 |
rs754962806 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808328 | TCAACTCACATTCTT[C/G]AAAGTTTTCGGGTGG | 254065 |
rs754964654 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724090 | AATCAATCATTGCTA[G/T]CAAGGACATACCTCA | 254065 |
rs754969328 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80717970 | TGTTTAAAATTTCTA[C/T]AATTATTTTAATTTT | 254065 |
rs755000778 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713692 | GAATGATCAATAAAA[A/G]AATAAAAAATAAAAA | 254065 |
rs755020492 | snp | A/C | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810504 | AATCAGCCGTGAAGC[A/C]TGTTTCCCCTTCTGA | 254065 |
rs755028150 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751223 | ATAATAAAATGTGTA[A/T]TTCAAAATTGCTAAA | 254065 |
rs755059869 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799903 | ACAGTCATCCACTCA[A/T]GCATTCATTCAGCCA | 254065 |
rs755059933 | in-del | -/AAGC | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811089 | TTTTTTTTCCTCAGA[-/AAGC]AAGCAATAACCACAG | 254065 |
rs755089711 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772946 | CTTGCAACAAATAAG[A/T]TGAATGATCAGGAAA | 254065 |
rs755098225 | snp | C/T | 2.28739e-05 | 0.00338178 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691080 | TTTTCAAGTCTCCGC[C/T]TGATGGTATTGAGGT | 254065 |
rs755116751 | snp | A/G/T | 5.03896e-05 | 0.00501924 | intron-variant | BRWD3 | GRCh38.p7 | X:80709401 | AAACAAAAAACTACA[A/G/T]CAAATAAATAATAGT | 254065 |
rs755125616 | snp | C/T | 2.60746e-05 | 0.00361063 | intron-variant | BRWD3 | GRCh38.p7 | X:80744285 | ACAATAGGTTTATAA[C/T]GAAGCAGAAATTCAC | 254065 |
rs755132116 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695227 | TAAGGCCTCCCGAGC[C/T]ATGTGGAAATGTGAA | 254065 |
rs755146624 | in-del | -/AT | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669086 | AGGAGATACCAACAC[-/AT]GTTTAGAGAAAGAAT | 254065 |
rs755157077 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751206 | GGTGACCACAGTTAA[C/T]AATAATAAAATGTGT | 254065 |
rs755179709 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783326 | GGGAGGCAGAGGTTG[-/C]AGTGAGATGAGATCG | 254065 |
rs755179715 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772181 | CACGTATGTTTATTG[C/T]GGCACTATTCACAAT | 254065 |
rs755181087 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787950 | TTAGCTGGGCGTGGT[-/G]GCGGGCGCTTGTAGT | 254065 |
rs755195348 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797691 | TACTCCTAACTATCC[C/T]TTTAAAGACTTGTAC | 254065 |
rs755197164 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714295 | TGCAATGGCGTGATA[C/T]GGGCTCACTGCAACC | 254065 |
rs755208556 | snp | A/G | 2.32145e-05 | 0.00340686 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691872 | CCGTTCACATTCTTC[A/G]TCTCTGGAATGAGCC | 254065 |
rs755221444 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80681030 | GTCCAGGTTGATCTC[C/G]ATCTCCTGGCCTCAA | 254065 |
rs755229255 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769602 | AAAGCAGTGTGTAGA[A/G]GGAAACTTACAGCAC | 254065 |
rs755233346 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80809096 | GGCCATCAACCCATT[C/T]CTCCCTCCACACTTA | 254065 |
rs755270226 | snp | A/G | 6.85377e-05 | 0.00585356 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681368 | GCAAAACTCTATTCC[A/G]AAATGATTTGGCTTT | 254065 |
rs755270948 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711214 | ATCTATACTTTTGTT[A/C]ATTCTAGATTAACAT | 254065 |
rs755273389 | snp | C/G | 0.000109072 | 0.00738405 | intron-variant | BRWD3 | GRCh38.p7 | X:80808988 | CACCTCAACCCTCCC[C/G]ACCCTTCCCGAAGGG | 254065 |
rs755280542 | in-del | -/CTCT | 0.0230396 | 0.104828 | intron-variant | BRWD3 | GRCh38.p7 | X:80742689 | TTACTCATGATTTGG[-/CTCT]CTGTTTGTCTGTTAT | 254065 |
rs755296499 | in-del | -/G | 2.29203e-05 | 0.0033852 | intron-variant | BRWD3 | GRCh38.p7 | X:80734222 | TGAACATACCACCTA[-/G]AAGATTAAAAAACAA | 254065 |
rs755310017 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766955 | TGGCACACTAGGAGA[C/T]TATAGCCCGCACCTG | 254065 |
rs755321709 | snp | A/G | 2.3107e-05 | 0.00339896 | synonymous-codon, intron-variant | BRWD3 | GRCh38.p7 | X:80684046 | ATAAGCTTTGGAGTT[A/G]TTGAATATTTGGCGA | 254065 |
rs755337449 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726450 | GTTTACAAACATCTG[C/T]TTTAAGATCACTGTT | 254065 |
rs755345704 | snp | A/G | 4.58742e-05 | 0.00478905 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728830 | TGCAGTAATAACTGT[A/G]GTATCATAGCGATCC | 254065 |
rs755346211 | in-del | -/ACCAACAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80686347 | GCAGCACACCAACAC[-/ACCAACAT]GGCATATGTATACGT | 254065 |
rs755350728 | snp | C/T | 2.29403e-05 | 0.00338668 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682619 | ATAATCGCAGCATCA[C/T]GCTATAGATCTGAGA | 254065 |
rs755372505 | snp | C/G | 0.000233146 | 0.0107944 | intron-variant | BRWD3 | GRCh38.p7 | X:80696706 | GTATTAAAATACACA[C/G]ACTCAAACAGAGACT | 254065 |
rs755373725 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80770188 | CTAAGAGGAGCTGGT[A/G]CCATTCCTTCTGAAA | 254065 |
rs755384569 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756968 | CAAGTCTAGAGATGA[A/G]CAATTTAACTTCCCC | 254065 |
rs755388353 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763871 | GTAGACATCAAGGAG[C/T]TTATTCTAAAATTCA | 254065 |
rs755395909 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801606 | AACATTTTGGGAGGC[A/G]TAGGTGGGCTGATCA | 254065 |
rs755396087 | snp | A/T | 4.63892e-05 | 0.00481585 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80729947 | CCATGTCTAGCACTA[A/T]ACTCTTCCATTCTTG | 254065 |
rs755407343 | in-del | -/CAAA | 0.00100143 | 0.0223543 | intron-variant | BRWD3 | GRCh38.p7 | X:80696710 | TAAAATACACACACT[-/CAAA]CAGAGACTCAGAGAT | 254065 |
rs755416618 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712210 | CCGAGCCGAAGCTGG[A/C]CTGTACTGCTGCCAT | 254065 |
rs755423137 | in-del | -/T | 0.000178158 | 0.00943648 | intron-variant | BRWD3 | GRCh38.p7 | X:80696914 | TATAATTACTTAACA[-/T]TTTGTATAATATTTC | 254065 |
rs755425175 | snp | A/G | 0.000165155 | 0.00908571 | intron-variant | BRWD3 | GRCh38.p7 | X:80735204 | GGGCGATCTCTAAAG[A/G]TAAAAATAAGGTGTT | 254065 |
rs755425207 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764473 | ACCACGCCTGGATAA[-/T]TTTTTTTTTTTTTGT | 254065 |
rs755429049 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726277 | ACGTTTACATGTTAT[A/G]TCTGTATAACATATA | 254065 |
rs755439154 | in-del | -/AC | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80686689 | ATTTACACACTGAAG[-/AC]ACAATTACATTTTTT | 254065 |
rs755439515 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765415 | GTCAATACAAGGCTG[A/G]TGATTAACAACAATA | 254065 |
rs755450312 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80780218 | ATAAAGTACTGAGTT[-/A]AACATATAGAACAAA | 254065 |
rs755465710 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778980 | CTCCAGCCAGGGCAA[C/T]AGAGCAAGACTCCAT | 254065 |
rs755470144 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778406 | GAGGTGCAGTGGGGG[A/G]TGAAGCAAGGAGAGG | 254065 |
rs755478069 | in-del | -/A | 7.26973e-05 | 0.00602855 | intron-variant | BRWD3 | GRCh38.p7 | X:80690101 | ATTCTCCTGTGAAAG[-/A]AAAAAATACTCTGTT | 254065 |
rs755487097 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721072 | GTCGAAATGATGATC[C/T]TTCAACTATTACTGT | 254065 |
rs755496648 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | BRWD3 | GRCh38.p7 | X:80707507 | AGTTTCATCTTCCTA[C/T]AACAAAGAGCCAGCA | 254065 |
rs755505269 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80709856 | TGTACAACGCAGAGT[A/G]ATAGTTTAGGCAGCA | 254065 |
rs755505467 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732811 | TTGAATTATATTCCA[C/T]AGACAGAGAAGAGGA | 254065 |
rs755519660 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80747884 | ATCAGAAAACAGAAA[A/G]TTTCACTCCTTCTTT | 254065 |
rs755525156 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725395 | ATATGACAAACAGAA[C/T]CTTTCAATAACACCC | 254065 |
rs755536405 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804567 | TGATACGAGACTCCT[-/A]AAAATGATTTAAAAA | 254065 |
rs755559222 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80686031 | AGGACATGAACTCAT[A/C]ATTTTTTATGGCTGC | 254065 |
rs755568969 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711421 | ACATCATACAACAGA[A/G]AAAGAAGGAAATCAA | 254065 |
rs755582551 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757687 | AAATTGTTCTCTAAC[-/AA]AAGACAAAATGAACT | 254065 |
rs755633947 | in-del | -/AAAA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746504 | GATTCTGCTCATGCT[-/AAAA]AACAAATCTTGATCT | 254065 |
rs755642382 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | BRWD3 | GRCh38.p7 | X:80725715 | ACATGCCTATATAAC[A/G]TATAACATGTTTACA | 254065 |
rs755647383 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700960 | GGTCCTAGAGCCAAT[C/T]CTGTGTGGATACCGA | 254065 |
rs755659760 | in-del | -/GGGGGCGGGT | 6.80133e-05 | 0.00583113 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809517 | TCCGGAGGGGCTGGC[-/GGGGGCGGGT]GGGGGCGCTGCCTCT | 254065 |
rs755672459 | snp | A/C | 3.60218e-05 | 0.00424377 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703582 | ACCTGCTATAGAAAC[A/C]AGTCCTCCTTTCTAA | 254065 |
rs755676312 | snp | C/T | 2.80804e-05 | 0.00374692 | intron-variant | BRWD3 | GRCh38.p7 | X:80685563 | AAGAACATATACTGG[C/T]TTCCAGACAACTATA | 254065 |
rs755691667 | snp | C/G | 6.44351e-05 | 0.00567568 | intron-variant | BRWD3 | GRCh38.p7 | X:80809047 | TGCACTAGCACCTGA[C/G]CAAAAGGGAAACACA | 254065 |
rs755697540 | snp | A/G | 2.30902e-05 | 0.00339773 | intron-variant | BRWD3 | GRCh38.p7 | X:80733540 | AATGGACTTATTTGT[A/G]AAATGAATTAAGTGC | 254065 |
rs755705744 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80793955 | AGGCTGAGGCAGGTA[C/T]ATCACTTGAGGTCAG | 254065 |
rs755712800 | snp | C/T | 9.14819e-05 | 0.00676259 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676799 | GGCAGTCTACTGAAA[C/T]GTCCTGAAAACATGG | 254065 |
rs755731765 | in-del | -/AAA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685997 | CTTTTACCTTTATTG[-/AAA]AGAAAAGTCCCTACA | 254065 |
rs755750417 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80701761 | GTTAAAAACCAATAA[C/T]ACACGTCATTAAGAT | 254065 |
rs755754227 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778897 | CCAGCTACTTGGCAG[A/G]TTGAGGCATGAGAAT | 254065 |
rs755754273 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769476 | TGGAAACTGAACAAC[C/T]TGCTGCTCAATGACT | 254065 |
rs755765132 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712132 | TAGGTCCAGGAGAGA[A/G]TTGTTTAAAATAAAA | 254065 |
rs755770036 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739441 | CTAAAAGATCCTAAA[G/T]GGAGATGGAAGTTTG | 254065 |
rs755779344 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792256 | AAGCTTTAAAGTTTA[C/T]ATCAGTTCTTCTTGA | 254065 |
rs755833043 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675384 | TTTGTTAAATTTTAA[A/G]ATTCAAATGAAAACC | 254065 |
rs755833605 | snp | C/T | 4.56106e-05 | 0.00477527 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719608 | AGAATGCTCTCATCT[C/T]GGTCATTGGTTTGCT | 254065 |
rs755847556 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759154 | CAAAGACTACATTAG[A/G]TTTCTTAAAATGCTG | 254065 |
rs755858855 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686621 | GTCTGAAATAAAAGT[C/T]GGAAAGAACAGCAAA | 254065 |
rs755862186 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752529 | TACCAACAGTGTGTT[A/T]AGAGTTCTTTTCTGC | 254065 |
rs755863613 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678074 | AAGAATCTGATTTAC[A/G]CTTTTAAAATAGTAT | 254065 |
rs755864958 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746964 | CACATAAGAGACCTG[A/G]GTAGTTATGTAATAC | 254065 |
rs755874512 | snp | C/T | 2.29334e-05 | 0.00338617 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691062 | ACAGACCTGTAAAAG[C/T]GATTTTCAAGTCTCC | 254065 |
rs755875307 | snp | A/G | 2.32016e-05 | 0.00340591 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686979 | GATTACACTTTAAAG[A/G]CTGTCTTCTGCCTCG | 254065 |
rs755910287 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725583 | CTGGAAAATACATTT[A/C]CTGCTAAAAAGAAAT | 254065 |
rs755914991 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80773960 | CTGAACACTTTGGAA[A/C]ATGCTTTACATATAT | 254065 |
rs755915143 | snp | A/G | 2.28938e-05 | 0.00338325 | intron-variant | BRWD3 | GRCh38.p7 | X:80744265 | AACCCTATAGTAACA[A/G]AAGGACAATAGGTTT | 254065 |
rs755920850 | snp | C/T | 2.34326e-05 | 0.00342283 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677261 | TCTTTATCTTCTCCT[C/T]CCATGTTTTCATCTT | 254065 |
rs755921454 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80753177 | TGTCTCTTCACTCTG[C/T]TGGTGCTTCTTTTGT | 254065 |
rs755925203 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736452 | ATATATACACTTATA[G/T]AAACAACTGTGGAAT | 254065 |
rs755940029 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80775213 | CCAGAAAGCCAAAAA[C/T]ATTTACTATCTGGCC | 254065 |
rs755969658 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784548 | TCCCTTCCCTCACCC[C/T]CACAAGAGGCCCTGG | 254065 |
rs755989855 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80763107 | ATTTAATGATTTTTA[A/T]ATGCCAGGCACTATT | 254065 |
rs755994510 | snp | A/C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773880 | TTAAGTCCTGTACTA[A/C/T]AATCACATTCTGGCA | 254065 |
rs756014507 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715449 | CTTCAAATTACCACA[C/G]TCTACAGAAATTATG | 254065 |
rs756025042 | snp | A/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675136 | TAAAACTGACCTTGG[A/T]ACTCAAGCTCACTTA | 254065 |
rs756029872 | snp | A/G | 2.27941e-05 | 0.00337587 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722685 | CCAAAAATGGAGGAG[A/G]CATGAGGTGAGGAGC | 254065 |
rs756035775 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80767029 | TCAGCAGTCTGAGAT[C/T]GACCTGCAAGGCAGT | 254065 |
rs756038920 | in-del | -/TTT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706044 | TTATACTTTTTAGTG[-/TTT]TTTAACTTTTTGACT | 254065 |
rs756058114 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703466 | AGAAAAAGGTTATAA[C/T]AGGTAATAATTACCT | 254065 |
rs756058389 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707989 | TGCCTTATACTCTAG[C/G]ATTAGTTTGATGCAC | 254065 |
rs756068083 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80785433 | TTTAAAGTGTTACAG[C/T]AGTTAGTGTGGAGAA | 254065 |
rs756095082 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716629 | AGCATGTTTATCCAC[A/G]TTGTAGCAGGTATCA | 254065 |
rs756132926 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80750191 | TCTAGCCAATGATTT[C/G]TTGGGTAGGACTCCA | 254065 |
rs756133474 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80729291 | ACCCATAGGTCTTAT[A/T]AAAAAGCAGATTTAG | 254065 |
rs756159408 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673296 | AAAAAAAGAAAAAAA[A/T]TTAAAAAGGGAAATA | 254065 |
rs756179992 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737890 | TCCACAAATTATGGC[C/T]AACACACCAAATTCA | 254065 |
rs756191311 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725831 | CCTATATAACATAAC[A/G]TGTTTACATGTGTTA | 254065 |
rs756197543 | snp | C/T | 2.43457e-05 | 0.00348888 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707476 | GATCCTCTACCGAAG[C/T]GTCACTTGTGCCAAC | 254065 |
rs756199548 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693640 | AATAAAGACACTGGC[A/G]GCATTTTGCCCATGC | 254065 |
rs756209248 | snp | A/T | 2.32285e-05 | 0.00340789 | intron-variant | BRWD3 | GRCh38.p7 | X:80684002 | ATTAACCCAACTAAT[A/T]ATCATACCCTTGACT | 254065 |
rs756213926 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767951 | GAAGCTTCAATAGCC[A/G]ATTCGATCAATTGGA | 254065 |
rs756223518 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80691751 | CTGCATATCCTTCTG[C/T]AGAACTTAAAACTTC | 254065 |
rs756245144 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784209 | AATATACACATCTAC[C/T]ATGTACCTATAAAAA | 254065 |
rs756289719 | snp | C/T | 2.85604e-05 | 0.00377881 | intron-variant | BRWD3 | GRCh38.p7 | X:80689756 | TCCTACTAATCATGC[C/T]GTGATTCTTACCTCC | 254065 |
rs756310556 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80688652 | CTGGGTAATATGTAG[C/T]AGAAAATAAAAAGTA | 254065 |
rs756314687 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80771623 | TTGACAAATGGGATC[C/T]AATTAAACTAAAGAG | 254065 |
rs756317464 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80807923 | CGTAACGATTATGCT[A/T]TTACTCAGTAGACCA | 254065 |
rs756319809 | snp | C/T | 2.33005e-05 | 0.00341317 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728810 | TTCAAAAGAAAATTG[C/T]TCACTGCAGTAATAA | 254065 |
rs756320500 | snp | A/G | 2.45743e-05 | 0.00350521 | intron-variant | BRWD3 | GRCh38.p7 | X:80690109 | TGTGAAAGAAAAAAT[A/G]CTCTGTTAGCCTTGG | 254065 |
rs756329396 | in-del | -/T | 0.0204488 | 0.0990265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679437 | AACCGAATATTTTTA[-/T]TTTTTTTATTTTTTA | 254065 |
rs756334765 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80713664 | CAAATCCCCCTCTGC[A/G]AGAGACACCCAAGAA | 254065 |
rs756366780 | snp | C/T | 2.53267e-05 | 0.00355847 | intron-variant | BRWD3 | GRCh38.p7 | X:80709396 | CTGGGAAACAAAAAA[C/T]TACATCAAATAAATA | 254065 |
rs756378031 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707140 | GTCATATGCACTCGA[C/T]CATTGACTGAAACAT | 254065 |
rs756398220 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751111 | AAAGGAGAGGGGTGA[A/G]GAAAGGGGAGATGCT | 254065 |
rs756398857 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80723282 | CTAAGATTCTATAAT[A/C]TTTCTCAAATTCACA | 254065 |
rs756401634 | in-del | -/AAG | 0.000166271 | 0.00911635 | intron-variant | BRWD3 | GRCh38.p7 | X:80692163 | CAGCTATTAAAAAAT[-/AAG]AAGATGCAAATCAAA | 254065 |
rs756404613 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766270 | ACCATCAGCTTTAAT[A/G]ATTCTCAGGCTTTTG | 254065 |
rs756430035 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80782299 | TAGGAAAATTGGATA[A/C]CCATATGCAGAAGAA | 254065 |
rs756442079 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755595 | ATACTTGAAGAGCCA[A/T]GAAAACATGCACATC | 254065 |
rs756442685 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741155 | ATGAGTGAGAACATG[A/C]GGTGTTCGGTTTTTT | 254065 |
rs756457327 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80705971 | TTACACTGAATTTAT[A/G]AAAAATATTTTTCTT | 254065 |
rs756458688 | in-del | -/C | 2.30489e-05 | 0.00339469 | intron-variant | BRWD3 | GRCh38.p7 | X:80688162 | GAAAAGACGTTAAGT[-/C]TACATTCAAAGTCAT | 254065 |
rs756460530 | snp | A/G | 2.28402e-05 | 0.00337928 | intron-variant | BRWD3 | GRCh38.p7 | X:80682422 | TAGGTAATACATACA[A/G]AATGCTTTGAGAACA | 254065 |
rs756460587 | snp | A/G | 2.29035e-05 | 0.00338396 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80693050 | ACTGCGGAATCTATC[A/G]CCTATAATGTTTTAA | 254065 |
rs756476354 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797363 | TCCTCTGGACCAACT[C/G]AAGATATTCAGTTGT | 254065 |
rs756477398 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80734364 | TTGGAGACATACTAG[C/T]GATTTAGAGAAAATG | 254065 |
rs756496951 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772710 | CACAAAACATTCAAT[C/T]ACCATATGATCCCCA | 254065 |
rs756508428 | snp | C/T | 6.84229e-05 | 0.00584865 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717654 | GTGGCCATCTGGCTC[C/T]GAGGAGCATTGTTAT | 254065 |
rs756532655 | snp | A/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674986 | GTATATACTAAGAAG[A/T]CTGTTTTATCCCATG | 254065 |
rs756542903 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778229 | ATCCAACTTTAGTAG[A/G]CCAGAATTTTGGGGG | 254065 |
rs756543658 | snp | C/T | 2.43013e-05 | 0.0034857 | intron-variant | BRWD3 | GRCh38.p7 | X:80719461 | ACAGTACATAAACTA[C/T]ACCCTTTACAAGTAT | 254065 |
rs756549795 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670227 | TGTGTTTTGTAGCAT[C/T]AAAAAGCCCTTAAGT | 254065 |
rs756563536 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80765203 | TGAAAGTTAAGACTG[C/T]TGCCCAGCCAATCAC | 254065 |
rs756566757 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756762 | ATATCACACACTTCC[C/T]TGGGGGGAGGAGAAT | 254065 |
rs756567145 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733718 | CCATATTTCAAGAGA[C/T]AAATAGTTCTGAATA | 254065 |
rs756569710 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80709037 | ATCTCTATGAGGGGT[A/G]AAGTCAATAATAACA | 254065 |
rs756586382 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80788453 | ACAGACTGGCAAATA[C/T]GCACATGAAAAGATA | 254065 |
rs756592599 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706595 | AACGGAAGGTATTCA[A/G]AGACAAAAACACATG | 254065 |
rs756596807 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799637 | AAAAATACAGCAAAG[A/C]TTTATATCAATGTAA | 254065 |
rs756597865 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762273 | CGTTAAAGATAAATT[C/G]TTAATGCAACTTCTC | 254065 |
rs756617015 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80726387 | TTATATCTGTATAAC[A/G]TAACATGTTTACATA | 254065 |
rs756620461 | snp | A/G | 0.000116043 | 0.0076163 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793797 | TATAAATAAAACACA[A/G]GAAAAACACATTTAT | 254065 |
rs756622501 | snp | A/G | 2.36723e-05 | 0.00344029 | intron-variant | BRWD3 | GRCh38.p7 | X:80725079 | GTCCCTATAATAAAA[A/G]TCAGTATTAACAATG | 254065 |
rs756646280 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728035 | TCTGATACATAAACA[C/G]CATGATATAGTATAA | 254065 |
rs756654733 | snp | C/T | 4.57169e-05 | 0.00478083 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682576 | TATTCAGAGATGATA[C/T]TTTTGATATGACTTT | 254065 |
rs756663854 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744423 | TAAATGATGTCCAAA[C/T]GATAGCAATAACAAA | 254065 |
rs756682365 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685853 | AGTAAGCTCATAGGA[C/T]GGTCTGATGTATTTC | 254065 |
rs756690610 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789197 | CAGATAGTCTATTTA[C/G]AAGACAAGCAATATA | 254065 |
rs756695531 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80726207 | ACGTTTACATGTTAT[A/G]TGTCTGTATAACATA | 254065 |
rs756701423 | in-del | -/TT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718202 | AAGTGTAAATAAATA[-/TT]TTTTTAAATCAAAAT | 254065 |
rs756702074 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80695386 | CAAAAAAGTTGATAG[-/T]TTTAAAAATCCTTAT | 254065 |
rs756712292 | snp | G/T | 4.50217e-05 | 0.00474435 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80791972 | ATAAAAAGAACAAAG[G/T]TTGCTAAGGAATAGA | 254065 |
rs756775207 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745789 | ATTTCATGAAATTAA[A/G]TCATAAATATTAAGA | 254065 |
rs756784981 | snp | A/C/T | 4.6027e-05 | 0.00479706 | intron-variant | BRWD3 | GRCh38.p7 | X:80681311 | TAAAGAAATAAATAA[A/C/T]AAATGTCTTGTCCTG | 254065 |
rs756793229 | in-del | -/AA | 0.000391773 | 0.0139905 | intron-variant | BRWD3 | GRCh38.p7 | X:80736092 | TGATGGACAAAACTT[-/AA]AAAAAAAAAAATCTG | 254065 |
rs756815250 | snp | C/T | 2.32331e-05 | 0.00340823 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80684097 | AGGACTACCATAGTT[C/T]CCTGCTTCCAAAGTT | 254065 |
rs756818268 | snp | A/G | 6.84635e-05 | 0.00585039 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734187 | TATTCTAATCACATG[A/G]TCAGTACTACCAGTT | 254065 |
rs756830519 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80695154 | ACTCTCTGTCTCCTG[C/T]AGCCATATGAAGAAG | 254065 |
rs756848191 | snp | C/T | 0.000117956 | 0.0076788 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809031 | ATGCTCCTCGAGCTC[C/T]TGCACTAGCACCTGA | 254065 |
rs756873186 | in-del | -/A | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671291 | CATATTTATTATCCT[-/A]AAAGTGACCCAAAGA | 254065 |
rs756892323 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80787597 | AAAAAAATGAATTCA[A/G]TCTAAACCACACACC | 254065 |
rs756892345 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719526 | ATTAACTGGTAAATG[C/T]GGAACATCTCCTTCA | 254065 |
rs756893071 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80803051 | AGCTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 254065 |
rs756899423 | snp | C/T | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673886 | GACCCAGATTTTACG[C/T]AGGTTTAAAGGGCCT | 254065 |
rs756916170 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684301 | TACCTCCCCACAACC[A/C]CAAAACATCTTTTGG | 254065 |
rs756929264 | snp | A/C | 3.29663e-05 | 0.00405981 | intron-variant | BRWD3 | GRCh38.p7 | X:80700068 | AAAATAGATAAGCTA[A/C]AACAGAAAACATAAG | 254065 |
rs756956915 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80685031 | AACGTTCTAAATATA[C/T]CTTATTTTCTTAAAT | 254065 |
rs756983037 | snp | A/T | 0.000231015 | 0.010745 | intron-variant | BRWD3 | GRCh38.p7 | X:80700085 | ACAGAAAACATAAGG[A/T]ATTAAACAGCAGCAT | 254065 |
rs756983142 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672892 | AATTCCAACTTGAAG[A/G]TAAGTACCAGTTGGT | 254065 |
rs756990910 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773190 | GCAAGTACTAAAAGT[G/T]TACAGAACTTAGCAT | 254065 |
rs757002409 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763679 | ATACATTTAACAGAA[C/T]ATGCACAGTATCTCT | 254065 |
rs757007089 | snp | A/G | 2.43143e-05 | 0.00348663 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707469 | ACAACAGGATCCTCT[A/G]CCGAAGCGTCACTTG | 254065 |
rs757013323 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80761098 | ATATTAACTGGTGAT[A/G]AACCAAAGAAAAAAA | 254065 |
rs757030431 | snp | C/G | 2.34996e-05 | 0.00342771 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80690062 | ATTATGTTCAATATA[C/G]CGTACCTCCCACATT | 254065 |
rs757036294 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751355 | AACATGACATTGTAC[A/G]CCTTGAATATACAAA | 254065 |
rs757043866 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757814 | AATAAACAGCCATCA[A/G]TGGACTTAGCTGCTT | 254065 |
rs757046649 | snp | C/T | 2.31728e-05 | 0.0034038 | intron-variant | BRWD3 | GRCh38.p7 | X:80688175 | AGTTACATTCAAAGT[C/T]ATATAAATTAGATGG | 254065 |
rs757066136 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762314 | TAACAAAACTAAGGA[C/T]CATGTTGATGAAGCA | 254065 |
rs757072732 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80784500 | CACCTAGGTATTGAG[C/T]CCCACATGCATTAGC | 254065 |
rs757086253 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769830 | GTTTTTTGACAAGAT[C/T]AACAAAACCGATAGA | 254065 |
rs757105952 | snp | G/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674888 | TGTACGCCTTCCTCT[G/T]CACTTAAGGGTTTTC | 254065 |
rs757106485 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755755 | TCAAGGGAATGGTTA[C/T]GTATTAAATTATGGA | 254065 |
rs757109407 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725314 | AAAGATAGTCTAAAC[A/T]GTTACAGCTCATTAA | 254065 |
rs757154085 | snp | G/T | 2.7115e-05 | 0.00368195 | intron-variant | BRWD3 | GRCh38.p7 | X:80744015 | ATGTTCAAGCTAAAT[G/T]TTATCACTTTTCTTA | 254065 |
rs757155643 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733094 | AAGATCGCACCACCG[C/T]ACTCCAGCCTCGGCA | 254065 |
rs757166724 | snp | C/T | 8.83158e-05 | 0.00664455 | intron-variant | BRWD3 | GRCh38.p7 | X:80735958 | TAAAAAATTAACATG[C/T]TTAATTTTTCACAAA | 254065 |
rs757174261 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80791590 | ATGGCTAAAAACGTC[C/T]ATACTATATTAAAAA | 254065 |
rs757200304 | snp | A/T | 2.28425e-05 | 0.00337946 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717710 | ACTACTATGTCTTCG[A/T]AGCCTGATGTTTGGG | 254065 |
rs757222567 | snp | G/T | 2.29158e-05 | 0.00338487 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677210 | TCTCCACTCTCTGAG[G/T]TGGATAAATGAGATT | 254065 |
rs757233558 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80701650 | AAATACATTAACATA[C/T]TCTACCAATCAATAC | 254065 |
rs757242188 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709027 | ACATTCAATGATCTC[C/T]ATGAGGGGTGAAGTC | 254065 |
rs757243558 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724554 | CAAACAACTTTCTGA[A/T]TACTAAATCATATGA | 254065 |
rs757257498 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80691529 | TCCTTACCAAGAAAC[C/T]CATCCAAAGTCAGGC | 254065 |
rs757259298 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736835 | AAAGGGAAAAGAACA[A/G]CTGAGCTCCTGATGT | 254065 |
rs757275914 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80690467 | TTATCTAATTACTTT[G/T]ATGATATAAATATTA | 254065 |
rs757276249 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724147 | GATTAAAAAAGAACT[A/G]AATGCAATCAAAATG | 254065 |
rs757294731 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715311 | CAAACATCAAAATGA[A/T]CTAATATTTGCAGAT | 254065 |
rs757301287 | snp | C/T | 2.35305e-05 | 0.00342997 | intron-variant | BRWD3 | GRCh38.p7 | X:80682127 | TAACAACGAGCATTT[C/T]TTTTTTTCTGTTAGC | 254065 |
rs757309033 | in-del | -/T | 2.86348e-05 | 0.00378373 | intron-variant | BRWD3 | GRCh38.p7 | X:80685439 | AACAATCAATATGTC[-/T]TTTAAGAGACTACCA | 254065 |
rs757322994 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789520 | AGCTGGGACTACAGG[C/T]GCGTGCCACCACGCC | 254065 |
rs757324245 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783683 | ACCTAAGTATCCAAC[A/T]CCAGACAACTAGACA | 254065 |
rs757327494 | snp | C/T | 4.67519e-05 | 0.00483464 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80725057 | AGAACGAATACTTCA[C/T]CATCATGTCCCTATA | 254065 |
rs757341444 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80767924 | TGGCATGAGAACTAC[A/G]TGACGCATGCAGAAG | 254065 |
rs757356262 | snp | C/T | 2.28167e-05 | 0.00337755 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682532 | TGTACCGTGGCCTTC[C/T]CCTCTTCTGACTCTG | 254065 |
rs757374270 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792467 | ATAGCTGTGTTTTTT[-/TC]TCTTTCATGTTTAAG | 254065 |
rs757384094 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804520 | TGGGATTACAGGCAT[A/G]AGCCACCACACCAGG | 254065 |
rs757428994 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670959 | TTTATCTTGAACCTA[C/G]TGGAATGTTTGCCAC | 254065 |
rs757431438 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80698977 | CAGCACTTTGGGAGG[A/C]CGAGGTGGGTGGATC | 254065 |
rs757441583 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80780546 | GTGGCAACAATCATA[A/G]CACTTCCATCTATTT | 254065 |
rs757453213 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800463 | GAGGATTGATTGAGC[C/T]CGGGAGGTGGAGGCT | 254065 |
rs757482190 | in-del | -/T | 0.00211976 | 0.0324867 | intron-variant | BRWD3 | GRCh38.p7 | X:80721315 | TTTCTTATTCATTTC[-/T]TTTTCAAGTTTATCT | 254065 |
rs757495444 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699862 | TACACAATCAACAGT[A/G]AAATATGCATAAAAC | 254065 |
rs757499531 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80805486 | TCCTTTTCATACCCC[A/T]ATACACCTTAAGTTT | 254065 |
rs757505015 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726454 | ACAAACATCTGCTTT[A/G]AGATCACTGTTGATT | 254065 |
rs757508334 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759672 | TTTAATGGTCCTTTC[A/G]GGCATTTCTATATGG | 254065 |
rs757524082 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80790324 | GAGAAAACTGCCTCA[A/G]ATCACAAACTGGAAA | 254065 |
rs757554335 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741128 | GGTGTTCTCATTGTT[C/T]AATTCCCACCTATGA | 254065 |
rs757584240 | in-del | -/ACCTTAC | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80764189 | TGAACGTTGACCTAA[-/ACCTTAC]ACCTTACAGAATTAA | 254065 |
rs757585628 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751064 | GATTTCATAAAAACA[A/G]AGTAGAAAGGTAGTT | 254065 |
rs757594585 | snp | A/G | 2.29516e-05 | 0.00338752 | intron-variant | BRWD3 | GRCh38.p7 | X:80716261 | GTACCCTAATAACAA[A/G]TCAAAGGTCAAAGTA | 254065 |
rs757615689 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80806854 | CTTTACAATATGAGG[-/A]AAAAGTCTAGTAAAC | 254065 |
rs757618205 | snp | A/G | 1.75188e-05 | 0.00295958 | intron-variant | BRWD3 | GRCh38.p7 | X:80691989 | GGCAGCTAGGTATAA[A/G]ATAAAAAAAAAAAAA | 254065 |
rs757641310 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678550 | TGGAGATATAATTGC[A/G]GAAATTTTCAGTAAA | 254065 |
rs757651221 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740778 | TGAAATAAAAAATCA[C/T]TGAAACTAAGAATAA | 254065 |
rs757651891 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713405 | ACCCCAACCCTGTGC[C/T]CTCTGAAACATGTGC | 254065 |
rs757663009 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80692162 | CCAGCTATTAAAAAA[G/T]AAGAAGATGCAAATC | 254065 |
rs757666031 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688497 | GATTACTCCATTGAC[A/T]TTTCAAGAAATAGGT | 254065 |
rs757675894 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771333 | GCTGGAGGCATCACA[A/C]TACCTGGCTTCAAAC | 254065 |
rs757676344 | snp | G/T | 0.00011419 | 0.00755528 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734202 | GTCAGTACTACCAGT[G/T]GTAATGAACATACCA | 254065 |
rs757691646 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694038 | ACAAGACCCAGGGCC[C/T]AGAAGGAAAAAATGG | 254065 |
rs757706013 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727618 | CAATAAAATATCAGA[C/T]AGTGATAAACCTAAT | 254065 |
rs757738401 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749253 | CTACATAATCTGTCC[A/G]ATGTTGAAAGTGAGG | 254065 |
rs757738555 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795842 | AGACTGCAGTGGGAG[G/T]ATTGCTTGAGCCCAC | 254065 |
rs757778693 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786757 | TGACCTGATGTGCCC[A/G]TCTCGGCCTCCCAAA | 254065 |
rs757784744 | snp | A/C | 3.32757e-05 | 0.00407881 | intron-variant | BRWD3 | GRCh38.p7 | X:80745738 | ATATTCACTGAAAAA[A/C]ATACGAAATTAACTT | 254065 |
rs757785047 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750973 | TGAAATTAGAAGACA[-/T]TATGCTAAGTGAAAT | 254065 |
rs757802741 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679224 | CTAAGGTGATAGCAG[C/T]AGAAACTATATAGAA | 254065 |
rs757824322 | snp | G/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810733 | CCAACCCTTGGTACC[G/T]CACTGACCTTCAGTA | 254065 |
rs757827985 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80705918 | GACCTAGAACATTAC[C/T]GTACACTACTGAAGA | 254065 |
rs757828493 | snp | A/G | 2.28334e-05 | 0.00337878 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717701 | TTCAATTTGACTACT[A/G]TGTCTTCGAAGCCTG | 254065 |
rs757836415 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761825 | CTCCACATCACATCA[G/T]TTCTTATTGGGACAC | 254065 |
rs757838662 | snp | A/C/T | 4.57548e-05 | 0.00478286 | synonymous-codon, missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677203 | TCCTAACTCTCCACT[A/C/T]TCTGAGGTGGATAAA | 254065 |
rs757844466 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704362 | CCACATGACAAGAAT[-/A]ATAATGTTGTCAGAT | 254065 |
rs757935305 | in-del | -/GAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802491 | TTAAGAAAATTAGGG[-/GAT]GATATCTCATCGACT | 254065 |
rs757935831 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732861 | AAGAACAATGTTGGC[C/T]GGGCATGGTGGCTCA | 254065 |
rs757937340 | snp | G/T | 4.63258e-05 | 0.00481256 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676921 | AGTGCCACCTCCACC[G/T]CTTCCTCGACTCCCT | 254065 |
rs757939997 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740625 | GTGGTGGCGCATGCC[A/G]GTAGTACCAGCTACT | 254065 |
rs757950969 | snp | A/G | 8.54774e-05 | 0.00653693 | intron-variant | BRWD3 | GRCh38.p7 | X:80695891 | TAATAGTTATTAAAC[A/G]ACAATTCTATATTTA | 254065 |
rs757957092 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718078 | TTTACAAATGTTTAT[C/T]AGTACTAGTTCAGGA | 254065 |
rs757964322 | in-del | -/CAAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685965 | AGGAAAGAAATCCTA[-/CAAT]CAAAGTTCTCATCCT | 254065 |
rs757969942 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785873 | TCTCTACTAAAAACA[C/G]AAAAAAGTTAGCCAG | 254065 |
rs757975218 | snp | A/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80754374 | CCTGAAACTTTACTG[A/T]ATTCATTTATCAAAA | 254065 |
rs757976645 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80683675 | ATTTGTTAGAATAAA[C/T]GGAACATACATGTTC | 254065 |
rs757981678 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80800667 | TAACTGGGTTTTCTC[G/T]TTTTGATGTCTACAA | 254065 |
rs757983584 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80694762 | TATTTATCCAATACC[C/T]GTACCCCCACTGTAT | 254065 |
rs758004353 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786574 | GGAATGCAGTCAGTC[A/G]TGCAATTTTGGCTCA | 254065 |
rs758016868 | snp | G/T | 2.29213e-05 | 0.00338528 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719519 | ATGCTCTATTAACTG[G/T]TAAATGTGGAACATC | 254065 |
rs758026091 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80795662 | AAGGTAGGAGAATCA[C/T]TTGAGCCCTGCAGTT | 254065 |
rs758036458 | snp | A/G | 2.44855e-05 | 0.00349888 | intron-variant | BRWD3 | GRCh38.p7 | X:80735243 | TCATCATGTTTGGCT[A/G]ATGGGCCAGAATGTT | 254065 |
rs758056160 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810371 | GTTTCTGTTTAAAAT[C/T]ATTATTATTTACCAA | 254065 |
rs758078367 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759579 | TCTCTCCAGCTCTTA[C/T]GTTTTAGCTATGAAT | 254065 |
rs758081610 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80710259 | CTCTAATTGGAAGCA[A/C]GACCCAAATATCAAC | 254065 |
rs758099909 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706825 | GCTTGAGCCCAGGAG[C/T]TCAAGGCATGCCTGG | 254065 |
rs758103425 | in-del | -/TGT | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80726043 | TATAACATGTTTACA[-/TGT]TATGTCTATATAACA | 254065 |
rs758104334 | snp | C/T | 2.48796e-05 | 0.00352693 | intron-variant | BRWD3 | GRCh38.p7 | X:80687028 | TTAATAGAGTTATAT[C/T]TAAAAGATCTTTCCT | 254065 |
rs758121711 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722140 | GGCGTGAGCCACCGC[A/G]CCTGGCCAGTCTGTG | 254065 |
rs758149499 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737210 | TTCCAGGACCTCCCA[C/T]GGATACTAAAATCAG | 254065 |
rs758162677 | snp | C/G/T | 2.31225e-05 | 0.0034001 | synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704723 | CCTTTCTTCTAGGGA[C/G/T]TTCAAATTTTCCTCA | 254065 |
rs758165346 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744854 | CCAAATACTTATGTG[A/G]CGCATTTAGAGCCAT | 254065 |
rs758181780 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697931 | TTCCCACCAGTAGTA[C/T]ATAAGCATTCTCCTT | 254065 |
rs758204123 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738024 | AGAGATTGTATGACA[A/T]GCTAAGCCTAAATAT | 254065 |
rs758206720 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792421 | TCATAACAGATAACA[G/T]CACTGCATATCAGAT | 254065 |
rs758227101 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786436 | GCATTTATCATTATA[C/T]TTAATGGTGAAAGAT | 254065 |
rs758240203 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684852 | AAAACAAGTTTCAGA[A/G]TGAAAACCATACTCA | 254065 |
rs758244523 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768659 | CATCAATGCTAGGAA[C/G]AAACTGCATCAACTA | 254065 |
rs758252599 | snp | A/T | 2.31374e-05 | 0.0034012 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80725029 | GATCCTTTGATCAAA[A/T]GGATGGGCTTCTAGA | 254065 |
rs758252724 | snp | C/T | 1.67354e-05 | 0.00289265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703610 | TAAAACATAAATACA[C/T]GAAAAGTATATGTAT | 254065 |
rs758258151 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80801549 | GGGTAACTTAAAATA[C/T]GAGAAATTAGGCCAG | 254065 |
rs758267148 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769815 | TGAATCCAGGAGCTG[G/T]TTTTTTGACAAGATC | 254065 |
rs758293714 | snp | C/T | 3.09818e-05 | 0.00393573 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745707 | ACTACAGCCGGTTAA[C/T]TGCCTGGCAGAGGTG | 254065 |
rs758301708 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723466 | GTTAGAATTACTCTC[C/T]TATTATACCTGGAAG | 254065 |
rs758315229 | snp | A/G | 6.89322e-05 | 0.00587038 | intron-variant | BRWD3 | GRCh38.p7 | X:80688143 | TAATTAAAAAGGAAG[A/G]GTGGGAAAAGACGTT | 254065 |
rs758315551 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80750443 | CATTTCTCAAAAGAC[A/G]ACATACAAATGGCCA | 254065 |
rs758322363 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753481 | TTGCCATGTTGGGCA[A/G]GCTGGTCTTGAACTC | 254065 |
rs758341049 | snp | C/T | 4.85743e-05 | 0.00492796 | intron-variant | BRWD3 | GRCh38.p7 | X:80735100 | TAAATATTCTAGATG[C/T]TCAAAACATTCCAGT | 254065 |
rs758345502 | snp | A/G | 2.43395e-05 | 0.00348843 | intron-variant | BRWD3 | GRCh38.p7 | X:80735240 | GTTTCATCATGTTTG[A/G]CTAATGGGCCAGAAT | 254065 |
rs758350654 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720959 | AGAACAACTAGCTAT[A/G]CCATATAAGAGTTTT | 254065 |
rs758360536 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711226 | GTTCATTCTAGATTA[A/T]CATTGAGGGCTAAAC | 254065 |
rs758363914 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715368 | GTTTATCAATTATGG[-/A]AAAAAAATGCAAATT | 254065 |
rs758368315 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788921 | GTCACAGAAAGATTA[C/G]TGGTTTCCAGGGGTT | 254065 |
rs758389387 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791309 | CATACTTTGTGAGGG[C/T]GAACTTTAATATAAA | 254065 |
rs758400749 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700924 | TATATAATGTCCTTG[C/T]AGATTCTGTTATTTG | 254065 |
rs758400893 | in-del | -/TTTC | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80688922 | ATTGGTATATCATGT[-/TTTC]TTTATTATGTAAGTA | 254065 |
rs758409132 | snp | C/T | 2.60437e-05 | 0.00360849 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691943 | ATTCTTCCTGGGAGA[C/T]AGGAACACCAGCACC | 254065 |
rs758417029 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700190 | TATTGAAAGACTTTA[C/T]ACAATAAAGGTTTCA | 254065 |
rs758419904 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729374 | AAAGTCATTTCTATA[C/T]TGCAACTAATGGAAA | 254065 |
rs758424678 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80707148 | CACTCGATCATTGAC[A/T]GAAACATCATTATGC | 254065 |
rs758444398 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732979 | ACTAAAAATACAAAA[A/G]CTTAGCCAGGTGTGG | 254065 |
rs758454244 | in-del | -/T | 0.0297427 | 0.118265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798394 | TCTTACCCCGAATAG[-/T]TTTTTTTTTACATTT | 254065 |
rs758465606 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743530 | CCATCTGGTCCTGGA[A/C]TTTTTTTGGTTGGTA | 254065 |
rs758470617 | snp | A/T | 0.00293685 | 0.0382073 | intron-variant | BRWD3 | GRCh38.p7 | X:80744295 | TATAATGAAGCAGAA[A/T]TTCACAATACCCCCA | 254065 |
rs758493211 | in-del | -/ACA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726060 | TTATGTCTATATAAC[-/ACA]ACATGTTTACATGTT | 254065 |
rs758498307 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80742802 | GATTTTGGGCTGAGA[C/T]GATGGAGTTTTCTAA | 254065 |
rs758515593 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672689 | TTCATAAAGCCTCAC[A/G]TTCCACAAAAATATT | 254065 |
rs758537826 | snp | A/C | 2.30218e-05 | 0.0033927 | intron-variant | BRWD3 | GRCh38.p7 | X:80681977 | AGATGCAGAACACCA[A/C]AAACAAAAGACATAT | 254065 |
rs758553585 | snp | A/C | 2.31401e-05 | 0.0034014 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723842 | TCTGGTGAAAATTTA[A/C]AATCAAACACCGCAC | 254065 |
rs758561788 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80789468 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 254065 |
rs758568588 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711352 | AGTCTCATCAGAGGG[C/G]TTTTACTTAACCCTA | 254065 |
rs758573361 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80681175 | CTGCTAATGGCCTGT[C/T]CCCAGTTATGAATAT | 254065 |
rs758576470 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731010 | CTGTGATGAACATCT[A/C]TATATAATCTTTGTA | 254065 |
rs758607184 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726723 | AAATACACCTTGCTG[A/G]AAGAAAATATAACTT | 254065 |
rs758607399 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697723 | CAGTCCACCACTGAC[A/G]GGCATCTAGATTGAT | 254065 |
rs758621972 | in-del | -/TT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790391 | TGAATTCTAAATAAC[-/TT]TTAAACTTAAGCATC | 254065 |
rs758628057 | in-del | -/TT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707799 | AATACATTAGAAACA[-/TT]GTTTTCAAAATGCCT | 254065 |
rs758635272 | in-del | -/TA | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670901 | ACACAAAATACACAG[-/TA]TATATATATATCAAA | 254065 |
rs758654723 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788916 | AGTCAGTCACAGAAA[A/G]ATTAGTGGTTTCCAG | 254065 |
rs758672244 | snp | C/T | 0.000142141 | 0.00842914 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745724 | GCCTGGCAGAGGTGA[C/T]ATTCACTGAAAAAAA | 254065 |
rs758677226 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802207 | ACACTTTAGGAGGTT[A/G]AGGTGGGCGGATCAC | 254065 |
rs758680386 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799441 | TACGCTATTTGTTTT[C/T]CAAGACCATGGCTAC | 254065 |
rs758680823 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747345 | GCAGGGTGTTTTGCA[A/G]CATCCCTCACCTGTC | 254065 |
rs758689028 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748764 | TCTTCCTTATTCCTT[C/T]CTTCTGCTAAGGTTG | 254065 |
rs758730582 | snp | C/T | 4.60193e-05 | 0.00479662 | intron-variant | BRWD3 | GRCh38.p7 | X:80682110 | CTAGAAGTAAAAATA[C/T]GTAACAACGAGCATT | 254065 |
rs758753885 | snp | C/T | 2.2945e-05 | 0.00338703 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709442 | CCTCTGAAGAACTGT[C/T]TGAGTCTTCCTGTAC | 254065 |
rs758764506 | in-del | -/A | 0.124444 | 0.216185 | intron-variant | BRWD3 | GRCh38.p7 | X:80736092 | TGATGGACAAAACTT[-/A]AAAAAAAAAAAATCT | 254065 |
rs758778029 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80721257 | TAACCAAGTGATCAG[A/T]TCTTACAAGAAATGT | 254065 |
rs758778983 | snp | C/T | 3.53732e-05 | 0.00420539 | intron-variant | BRWD3 | GRCh38.p7 | X:80709604 | AAGAATAATAAATTT[C/T]AAAAAAGGAAAAGCT | 254065 |
rs758782024 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804591 | TTAAAAATCTTAAAA[C/T]GTGGTTTTTAAAAAG | 254065 |
rs758790522 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739739 | CCTACACACCTATAA[A/G]CTTAATTTATAAATT | 254065 |
rs758800773 | snp | C/T | 5.03392e-05 | 0.00501668 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685488 | ATGAATCTTGTTGTC[C/T]TTCTGGAACAACAGA | 254065 |
rs758803997 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80698789 | CTTTTACTTGATGAC[A/G]AATAGATGGGAGCTG | 254065 |
rs758804572 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80752984 | TTTTTTTGTATACCT[-/G]GTTGGCCATTTGCAC | 254065 |
rs758805329 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714889 | TAACAAGAATTGGCA[C/G]TATGTTCATTTAGTA | 254065 |
rs758806992 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748012 | TAAGTGGCGAGAATG[G/T]GCATCTTTTTATTAG | 254065 |
rs758813360 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703267 | AATATTCAATGAGCA[A/T]CTAATAGACTGAAGC | 254065 |
rs758817454 | in-del | -/CTTT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680710 | ACTTTGGAAACTCTC[-/CTTT]CTTATTAATATGAAA | 254065 |
rs758821389 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727442 | CTGCTCTCTGTGATA[C/T]AGCTAAATTGGCTTT | 254065 |
rs758826031 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80678472 | GACAAGACATTTTTT[A/T]AAAAAAAAGAAATAA | 254065 |
rs758832256 | snp | C/G | 5.97158e-05 | 0.00546391 | intron-variant | BRWD3 | GRCh38.p7 | X:80809315 | CAGCTCTGGGGAAGA[C/G]GGGGGAAAAGAGGTT | 254065 |
rs758833485 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748590 | TTGTCTGTTCAGTTT[C/T]CACTTTCATCTCTGA | 254065 |
rs758835199 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758552 | TGGCCAATTCATATG[C/T]ACAGCTGCTCTAATT | 254065 |
rs758839631 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686765 | GGAAAAAAAGAAAGG[-/A]AAAGGAGAGGTGAGA | 254065 |
rs758850910 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782013 | AGAAATAATCCTAAA[A/G]TGTATATGGAACCAC | 254065 |
rs758858991 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80771265 | CTTTAAAGTTCATAC[A/G]GAACCAAAAAAGAGC | 254065 |
rs758868273 | snp | C/T | 4.66614e-05 | 0.00482996 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80729987 | CTGCCAAATTCTTGC[C/T]GTTCCATCTCGACTT | 254065 |
rs758880996 | in-del | -/AACAA | 0.00370467 | 0.042879 | intron-variant | BRWD3 | GRCh38.p7 | X:80740730 | TCCAGCATGGGTGAC[-/AACAA]AACAAAACAAAACAA | 254065 |
rs758935719 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771212 | TGCCATCCCCATCAA[C/G]CTACCAATAACTTTC | 254065 |
rs758952494 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80713376 | CCTTGGGATCCTGTT[A/G]ATCTATGACCTTAAC | 254065 |
rs758956506 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795169 | CATTTTTAATCTAAG[C/T]TAATGTACAAATCCC | 254065 |
rs758975232 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80805374 | TATGAACAAAAAGGC[A/T]GGATTTTTGTCTCAT | 254065 |
rs758981863 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749850 | TAAAATGTATGATAA[A/G]GCTTATTTAATAGAA | 254065 |
rs758984753 | snp | A/C | 2.37076e-05 | 0.00344286 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704696 | CTTTCTAGTCTGCTT[A/C]GGTTTCTTCTGCCTT | 254065 |
rs758992307 | snp | A/T | 0.000529661 | 0.016265 | stop-gained, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677304 | TAAGTAGTTTTCTCT[A/T]GATTCCTGTCCGGGG | 254065 |
rs758996970 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80759259 | CTGTTGAATAAACCT[A/G]TCTAAAATTTTGTCT | 254065 |
rs759017590 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699728 | CTCCTGCTTTGCTCT[-/A]AATTATGGACTAGTA | 254065 |
rs759038633 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721975 | CCTCATCCACCCAAG[C/T]AGTTGGGATTACAGC | 254065 |
rs759042186 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725926 | ACATGCCTATATGAC[-/AT]AACTTGTTTACATGT | 254065 |
rs759042642 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80712737 | GCCCATCGTCTGAGA[C/T]GTGGGGAGCGCCTCT | 254065 |
rs759046796 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727491 | CTCAGGACCTTTGCA[C/T]ATGCCGTTCCCTCTT | 254065 |
rs759065310 | snp | C/T | 0.000124297 | 0.00788245 | intron-variant | BRWD3 | GRCh38.p7 | X:80728715 | AAAATAATGTGCTTT[C/T]TGACCATTTTAATTA | 254065 |
rs759069971 | snp | A/G | 2.87981e-05 | 0.0037945 | intron-variant | BRWD3 | GRCh38.p7 | X:80707407 | AATAATTTTGACCAA[A/G]TTAAAACCATTAAAA | 254065 |
rs759071547 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748622 | TCTGAGTCTTTTCTT[C/T]TGTTTTTTTTCCTAA | 254065 |
rs759080454 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799188 | ACTTCAGAATCATTA[C/T]GACAACTGAGAAAAT | 254065 |
rs759115822 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80713165 | AGGAGCCCCTCTGCC[C/T]GGCCACCACCCCGTC | 254065 |
rs759159737 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80741377 | ATAAACATCTGTGTG[C/T]GTGTGTCTTTAGAGC | 254065 |
rs759166424 | in-del | -/ATATAT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795523 | TATGTATACATATAC[-/ATATAT]GTGTGTATATATATG | 254065 |
rs759175217 | in-del | -/TATATG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795496 | ATACATGTATGTGTA[-/TATATG]TATATGTATGTATAC | 254065 |
rs759176317 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771925 | ACAGTGAGATACCAT[A/C]TCACACCAGTTAGAA | 254065 |
rs759195409 | in-del | -/AGAAAT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733214 | GACGTGGGTGCTAAC[-/AGAAAT]AGAGCAAAATAAACA | 254065 |
rs759199855 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80682776 | ACTAAAGTAAGATAC[C/T]ATTTTCACCTAAAAT | 254065 |
rs759213645 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713517 | TAAGAGTCATCACCA[A/C]TCCCTAATCTCAAGT | 254065 |
rs759215140 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80764030 | AACACACAAATCAAT[A/G]GAACAGAATAAAGGG | 254065 |
rs759232888 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669645 | GGGAGGAGGGAACAC[A/G]TTAGCAGTTTCCTTG | 254065 |
rs759234406 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787418 | CCAAAACAATTTTTT[A/G]AAAATGAGAGCAAAG | 254065 |
rs759248917 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80678863 | CCTAATCCCCGAAGT[G/T]ACTGCAGTTGGAGAT | 254065 |
rs759266258 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722843 | TTTATAAGTAAATAC[C/T]TGTTTTCATTCCTTG | 254065 |
rs759270846 | snp | A/C | 3.39018e-05 | 0.004117 | intron-variant | BRWD3 | GRCh38.p7 | X:80689887 | TTCAGTAATTTTTAC[A/C]ATTTTTCAATTAATT | 254065 |
rs759279895 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734007 | CAAGAGTAAAGTGTA[A/C]GCCAAAATTTGTGAT | 254065 |
rs759288990 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80806358 | CACTAGTAATGAAAA[A/G]AAAAGAGCTACTTAA | 254065 |
rs759292254 | snp | C/T | 3.55467e-05 | 0.0042157 | intron-variant | BRWD3 | GRCh38.p7 | X:80791827 | AGAATCAACAATCTG[C/T]TTATAACACACAGGT | 254065 |
rs759312206 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796729 | AGATTTGCATCTCCA[G/T]GGTTTAGCATCAGGA | 254065 |
rs759354432 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710299 | TGGCTGGAGACCATA[C/T]GGTGTTAGGCTACTT | 254065 |
rs759369095 | snp | C/T | 4.57368e-05 | 0.00478187 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682083 | TTCATTTGTTTCTGC[C/T]TCCCTTTTGGACTAG | 254065 |
rs759390344 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80741389 | GTGCGTGTGTCTTTA[C/G]AGCAGCATGATTTAT | 254065 |
rs759391038 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754995 | CCTGGGCAACAGAGC[A/G]AAACTCCGTCTCAAA | 254065 |
rs759396242 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726128 | GTATAACATATAACA[C/T]GTTTACATATGTCTG | 254065 |
rs759396382 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764602 | ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCTTAGG | 254065 |
rs759396994 | snp | A/G | 4.56673e-05 | 0.00477824 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692941 | ATAAACATACTTACT[A/G]AACACTGTAACACTG | 254065 |
rs759406631 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80696159 | CTGACCTGTTTGGGA[A/G]TGCCCTGCCTACTGC | 254065 |
rs759414601 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706404 | GTGAGCCACCACGTT[C/T]GGCAAATTTTTTCTT | 254065 |
rs759415396 | snp | C/T | 4.56038e-05 | 0.00477492 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717585 | CACCTACTAACCCCA[C/T]TATTTAGTTCATTGA | 254065 |
rs759416249 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80705492 | AAACTGAAATAAATA[C/T]ATATACAGTCATATA | 254065 |
rs759431495 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80777387 | GTATACAAATTAGTG[A/G]TATTATTATTATTTT | 254065 |
rs759433212 | snp | G/T | 2.28812e-05 | 0.00338232 | missense, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793624 | CTGAAAATCTCACCT[G/T]TGGCATCCCGTAGCA | 254065 |
rs759433345 | snp | C/T | 2.30354e-05 | 0.00339369 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80724964 | CGAATTTTGGTCCCC[C/T]GGTCAAGGTCCCAAA | 254065 |
rs759439260 | snp | C/T | 2.28136e-05 | 0.00337732 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682492 | CTACTAGATAATGAA[C/T]TGCTGCTGCTTCTTA | 254065 |
rs759462028 | in-del | -/CTC | 2.28154e-05 | 0.00337745 | cds-indel, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682531 | CTGTACCGTGGCCTT[-/CTC]CTCTTCTGACTCTGG | 254065 |
rs759490285 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80723733 | TACTCTACAGCAAAA[A/T]TTAAATATGCTAACC | 254065 |
rs759496902 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761186 | AGTGGTTATACTAAC[C/G]ATACTTTATTAGTGC | 254065 |
rs759506609 | snp | C/T | 2.28087e-05 | 0.00337695 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734153 | CAATTTTCTCAGGAA[C/T]CTCAGAACCCAAATA | 254065 |
rs759514806 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794379 | GGTATGGTGGCTGCA[A/C]CTCTAATCTCAGCTA | 254065 |
rs759547466 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698904 | ACATCTAAATCAAAT[A/C]TTTATCTTAATAAAT | 254065 |
rs759571830 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754843 | GAAACCCCATCTCTA[C/T]TAAAATAACAAAAAA | 254065 |
rs759585063 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80756232 | ATTAAGAAATAACGT[C/T]GGCTCATGCCTGTAA | 254065 |
rs759596840 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762900 | CTTTCCTCTCTGGGG[C/T]CTCAGTAGTCTCACA | 254065 |
rs759602052 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730816 | CTACAAAAAATTGAA[C/T]TGAACTACATATGTT | 254065 |
rs759615410 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762191 | AAGTAGTTTACAAGC[A/C]AACATGTTTTGCCTT | 254065 |
rs759617516 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676324 | TCTGTAGTGTCTGTG[C/T]TGTGTTTCGTGTGTG | 254065 |
rs759659309 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752353 | TGTGAATAGTGCCAT[G/T]ATAAACATACTAGTG | 254065 |
rs759662872 | snp | A/G | 2.43448e-05 | 0.00348881 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709564 | GAACGCCCACAGCTA[A/G]GCTCATAATCATTCT | 254065 |
rs759663830 | snp | A/T | 0.00158814 | 0.0281345 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809710 | GAGAGGGAGAGAGAG[A/T]GTGAGTGAGTGAGAG | 254065 |
rs759668223 | in-del | -/T | 0.0132004 | 0.0801621 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80791992 | TAAGGAATAGAGCAG[-/T]TTTTTTTTTAACCAT | 254065 |
rs759671390 | snp | A/G | 2.30718e-05 | 0.00339637 | intron-variant | BRWD3 | GRCh38.p7 | X:80733448 | ACAAATATGTATTAC[A/G]TAATTACCTGTCTCC | 254065 |
rs759673084 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771547 | AAAACTGGCTAGCCA[C/T]ATGTAGAAAGCTGAA | 254065 |
rs759673268 | snp | A/C | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792866 | TGAGTAGAAAAGCTT[A/C]TTTAACAATTACTGA | 254065 |
rs759706159 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712513 | ACAACCTCCACCTCC[C/G]AGCCGCCTGCCTTGG | 254065 |
rs759717914 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739193 | ATACACTTTGATGGT[A/G]GAACCAACATGATTT | 254065 |
rs759729721 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80745922 | AAGCACCAAGAATAC[G/T]CTTCCATTAAATCCC | 254065 |
rs759732041 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715302 | TTAAGAAAGCAAACA[C/T]CAAAATGATCTAATA | 254065 |
rs759733268 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772730 | TATGATCCCCAATTA[A/C]AAACTTGGGCATTTA | 254065 |
rs759733582 | snp | A/C/T | 0.00105918 | 0.022993 | intron-variant | BRWD3 | GRCh38.p7 | X:80701617 | AGTAACAAAAAATAC[A/C/T]ATATTATGAGATTTC | 254065 |
rs759743126 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731861 | GATCACACCACTGCA[C/T]TCCAGCCTGGGTGAC | 254065 |
rs759768043 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80692285 | TGAAAGTACAACTCC[A/G]GTTACATACAGATAA | 254065 |
rs759779306 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722085 | ATGCCTAACCTCAAG[C/T]AATCCACCCGCCTTG | 254065 |
rs759779733 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670819 | AACAACTTATCTCCA[C/T]TTCAATCTCTGAATA | 254065 |
rs759788450 | snp | A/G | 4.57033e-05 | 0.00478012 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716199 | CTTCTTTTCAACTGT[A/G]TAAAGACTGATTTCT | 254065 |
rs759790466 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80773653 | ACTCTTCCAGGGCAT[A/G]AATTCTCCACTTGAA | 254065 |
rs759802290 | snp | C/T | 2.71846e-05 | 0.00368668 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80700011 | AACACTGTATATTTT[C/T]GATTTCCTTACAGCC | 254065 |
rs759807600 | snp | A/C | 2.28781e-05 | 0.00338209 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676792 | AATTCGAGGCAGTCT[A/C]CTGAAACGTCCTGAA | 254065 |
rs759812824 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806155 | TTACAAAGAAGTCCA[C/T]AGGTAGAGAACAGAC | 254065 |
rs759820759 | snp | C/T | 2.28339e-05 | 0.00337882 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722587 | ATATCCCAGCTGTGG[C/T]ATAAGCTGTTCATCT | 254065 |
rs759841142 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790887 | AATTCTGGTGGATAA[A/T]CAAACAACTCTTGGA | 254065 |
rs759861411 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702373 | TAGACAGGAGTCTCA[C/T]TAGGTCTTAGAGTGT | 254065 |
rs759866301 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783256 | GCCAGGCATAGTAGT[A/G]CACACCTGTAGTCCC | 254065 |
rs759872304 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737461 | TTTGTTCCTCAGCTG[C/G]TTGAAGCCACAGATG | 254065 |
rs759904244 | in-del | -/AAGT | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80682765 | CTTCTCAAATAACTA[-/AAGT]AAGATACCATTTTCA | 254065 |
rs759911971 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753791 | GGTGTCCTTTTCCCA[A/G]TGCATGTTCTTGTCA | 254065 |
rs759948722 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714801 | TTATATCCCATTGAG[G/T]ATTATTTCTACTATT | 254065 |
rs759963924 | snp | A/C | 2.49897e-05 | 0.00353472 | intron-variant | BRWD3 | GRCh38.p7 | X:80722838 | GGGAATTTATAAGTA[A/C]ATACTTGTTTTCATT | 254065 |
rs759964928 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789905 | ATATACCAGGCAGGC[A/G]TGGTGGCTCACACCC | 254065 |
rs759980524 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697463 | TAAGTTTTTAACCCC[-/T]ATCCCCCTCCTAATC | 254065 |
rs759983744 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810189 | TCCCCCTGGGTTGAT[C/T]TTGAGGAACTTAAGA | 254065 |
rs760037253 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80693324 | TTTTCAATTAATTAG[C/T]ATCATCATTAGGCAC | 254065 |
rs760045218 | snp | A/G | 0.000112126 | 0.0074867 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809302 | CGATCAGGTAATACA[A/G]CTCTGGGGAAGAGGG | 254065 |
rs760050657 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80708707 | TGTAATCCCAGCTCC[A/T]GGGGAGGCCAAGGCA | 254065 |
rs760054841 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789440 | GAGTGCAGTGGCGCG[A/G]TCTCGGTTCACTGCA | 254065 |
rs760058219 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80727249 | CACTCTTAGCCCATT[C/T]CAATCTATTCCCTCT | 254065 |
rs760065405 | snp | A/C | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671345 | AACAAAAAACAAAAC[A/C]TTTTCTTTGATAGGA | 254065 |
rs760075274 | snp | C/T | 2.61056e-05 | 0.00361277 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685463 | ACTACCAGGCCTACC[C/T]CAGAAAGAGATGAAT | 254065 |
rs760079855 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701883 | CCATTTCCTCTAGGA[C/T]ATGGAAACTCATGTA | 254065 |
rs760082978 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80779698 | AAGAAGCCACGAAAG[C/T]GACAAAAATGAATAT | 254065 |
rs760088107 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80698479 | TTTTGGAGGCCAAGT[C/T]GGGTGGATCACCTGA | 254065 |
rs760098886 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728062 | ATAAAGACAACTGAG[A/T]TGAGTCAGAAGAATT | 254065 |
rs760109548 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80767251 | AACTGCCTCCTCAAG[A/G]GGTTCCCTGACCCCT | 254065 |
rs760115094 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674080 | AATTTGCATGCAAAC[A/G]GAAAATTATCTGTTT | 254065 |
rs760128544 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80692907 | TACTACTACAATGTC[A/G]TATTAGGCATAAAAG | 254065 |
rs760128780 | snp | G/T | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703516 | AAATGGGGAACGTCG[G/T]GGTATAGTATCCAAG | 254065 |
rs760136831 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758239 | AAAAAGTCAAACGAG[G/T]TCTCTGTCCTCGTGG | 254065 |
rs760159337 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736667 | ATCGTTATTCGTATC[A/G]TATCATTGTGGGAAA | 254065 |
rs760165297 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758181 | TCCAGTCAGGGCAAC[A/G]AGAGCGAAACTCCAT | 254065 |
rs760166045 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80768159 | GGAAAACACTCTTCA[G/T]GATATTTTCCAGGAG | 254065 |
rs760166411 | snp | C/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80676488 | ATACTGGCATAAATG[C/G]AAAAGCACCAATGTG | 254065 |
rs760186891 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727386 | AAATCCTAGTCTGGC[C/T]CCTGTCCACTTTTCC | 254065 |
rs760189822 | snp | A/G | 7.25742e-05 | 0.00602344 | intron-variant | BRWD3 | GRCh38.p7 | X:80745774 | TTAAAAGTGAAACTG[A/G]TTTCATGAAATTAAG | 254065 |
rs760220985 | snp | C/T | 9.2202e-05 | 0.00678915 | intron-variant | BRWD3 | GRCh38.p7 | X:80724930 | CAGGTAGGTGTCTCT[C/T]ACCATGTTAAAGTAA | 254065 |
rs760246484 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80720881 | TATACAAATATGTAC[C/T]ATTGTATGTATAACT | 254065 |
rs760285856 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715779 | TAACAGAAATAGGTA[C/G]CAGAACTGATTTGGC | 254065 |
rs760304045 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80712601 | AGGAGCGTCTCTGCC[C/T]GGCTGCCCATCGTCT | 254065 |
rs760307423 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697595 | CTTTCTGTTTTTCAG[A/C]TGTTTTACTTACGAT | 254065 |
rs760310598 | snp | C/G | 0.000946163 | 0.0217298 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809479 | GCCGCCATCCTTTTC[C/G]CGAGGGGGTTTGGGG | 254065 |
rs760323780 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750055 | GCAAAAGAATGAAAT[C/T]GAACCCTATTCTCCT | 254065 |
rs760332063 | in-del | -/AGTTTTAG | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80740934 | TTAAATTATACTTTA[-/AGTTTTAG]AGTACATGTGCACAA | 254065 |
rs760341833 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687326 | CCTTAATATTTGCCG[G/T]TAGTTAAGTATACTT | 254065 |
rs760380538 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728022 | AACTTTACATCCCTC[C/T]GATACATAAACACCA | 254065 |
rs760415077 | in-del | -/T | 0.32179 | 0.239607 | intron-variant | BRWD3 | GRCh38.p7 | X:80682123 | ATGTAACAACGAGCA[-/T]TTTTTTTTTTTCTGT | 254065 |
rs760431961 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80698287 | ATAGGTATAGGGTCC[C/T]GCTTAAAGTTATATA | 254065 |
rs760464054 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732223 | AAAATATCCACTTCC[A/G]GTATACCAAGCATTT | 254065 |
rs760477889 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679511 | AAGCTCTGCATATGC[A/G]TTTGGAGAGTCATCA | 254065 |
rs760487609 | snp | C/T | 5.88504e-05 | 0.00542418 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745690 | AAAATATGACCAAAG[C/T]GACTACAGCCGGTTA | 254065 |
rs760494462 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80749630 | GTCATGGTTTTTCAT[C/T]CATTCAGCAGCTCAA | 254065 |
rs760502480 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713051 | CCCGGCCAGCTGCCC[C/T]GTCTGGGAGGGAGTT | 254065 |
rs760503212 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728546 | AGACTTAGAAAAGAT[A/C]TTGAAAAGATTTCAT | 254065 |
rs760514110 | snp | C/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669303 | TTTTTCTTATGAAAA[C/T]GACTAACCACATTTA | 254065 |
rs760517422 | snp | A/G | 2.31581e-05 | 0.00340272 | intron-variant | BRWD3 | GRCh38.p7 | X:80691816 | AATTTTTTCACATTC[A/G]TCATACCCAGGGAAA | 254065 |
rs760529349 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678265 | ACCTTTAATTTCAAA[C/G]GTTGAACTGATGGGA | 254065 |
rs760529540 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708095 | GCTGTTATCACATTA[C/T]ATTTAAAAGGGAGCA | 254065 |
rs760537371 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80705195 | CACTTGAATCCAAGA[C/G]GCAGAGGTTGCAGTG | 254065 |
rs760541163 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80786231 | TCTCAGTTGCAATCA[C/T]CTCCATTGTCACAGA | 254065 |
rs760542403 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763913 | CCTAGAATATAGAAA[A/G]CAATCTTTACAAAAC | 254065 |
rs760546317 | snp | C/T | 2.28964e-05 | 0.00338344 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716165 | TACTTACCCTTTGAG[C/T]AGTGTAAGATGGCTT | 254065 |
rs760551865 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740434 | ATTAAAAGAAGCCAA[A/C]GTATTCCACATTAAA | 254065 |
rs760555903 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761056 | TATCTCTTAAAACCT[A/G]TTGGTTAGCTTAGTA | 254065 |
rs760562830 | snp | C/T | 4.73294e-05 | 0.00486441 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709552 | GTCCTGCGTAAAGAA[C/T]GCCCACAGCTAGGCT | 254065 |
rs760564584 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80771089 | TACAAACCTGCTCAG[C/T]GAAATAAAGTAGGAC | 254065 |
rs760581657 | snp | C/T | 0.000173158 | 0.00930316 | intron-variant | BRWD3 | GRCh38.p7 | X:80692040 | ATATCATGTGATTAC[C/T]ATTTTACTTTTAAAA | 254065 |
rs760607919 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688206 | ACATTTACAAATAAA[C/T]GGGAAATAAAATCAC | 254065 |
rs760610549 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798900 | TAACCCCACACCTTA[C/T]AGAAGAGAAAACAGA | 254065 |
rs760624959 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80704002 | TAAAATAACTACATA[C/T]ACCAAGTCTTTAAAT | 254065 |
rs760627318 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80795455 | CGTATATGTATGTGT[A/G]TATGTATAGATACCT | 254065 |
rs760636883 | snp | A/C | 5.21404e-05 | 0.00510563 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809270 | TTTGTTGCAGGGTCC[A/C]GACTGCAAGAACCTA | 254065 |
rs760675783 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802443 | CAAGACTCTCATCTT[-/A]AAAAAAAAAAAAAAA | 254065 |
rs760679028 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784869 | CCTGTATTTTTAAAA[C/T]AGAATGATTTGTATT | 254065 |
rs760681038 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810245 | CCCCTTTTTCCTCCC[A/G]GTACCAAAGCGGTTT | 254065 |
rs760715573 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769486 | ACAACCTGCTGCTCA[A/G]TGACTACTGGGTAAA | 254065 |
rs760716231 | snp | C/T | 5.22432e-05 | 0.00511066 | intron-variant | BRWD3 | GRCh38.p7 | X:80681524 | TAAAAGATTTTAATA[C/T]TAACATAATTATCAT | 254065 |
rs760721996 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725978 | AACATGTTTACATGT[-/TA]TATGTCTATATAACA | 254065 |
rs760737549 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80769729 | GTTAGCAGAAGGCAA[G/T]AAATAACTAAGATCA | 254065 |
rs760738184 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731894 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 254065 |
rs760751197 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738582 | CTACAGACAAAAAAA[A/T]GAAACAGAAGGGAAG | 254065 |
rs760753982 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778420 | GATGAAGCAAGGAGA[A/G]GAGTGCCTTCAGCAA | 254065 |
rs760765464 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674700 | AAAAAAAGACTACAA[C/G]AAAAAAATAGCTTGG | 254065 |
rs760769986 | snp | C/T | 3.99218e-05 | 0.00446758 | intron-variant | BRWD3 | GRCh38.p7 | X:80699944 | GCATAGCTTATGAAT[C/T]TGGCAAACTTACCCT | 254065 |
rs760804903 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685657 | ATGTTTTATCGGCTG[C/T]ACTTTAAGGTGAAGG | 254065 |
rs760825838 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762891 | TCCCCTTTCCTTTCC[A/T]CTCTGGGGTCTCAGT | 254065 |
rs760825976 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80803953 | TCAAATGAGATAATG[C/T]GAAAACACTTTTAAA | 254065 |
rs760853199 | in-del | -/T | 8.54482e-05 | 0.00653581 | intron-variant | BRWD3 | GRCh38.p7 | X:80730070 | AAAAATGTAAATCAC[-/T]TTTTTTTTGATAATA | 254065 |
rs760854594 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762060 | CTCAAGATAAAAAAA[C/T]GCAAGAGACAAAAAA | 254065 |
rs760864482 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730731 | CACCCATACTTCTGT[C/T]ACTGTTAACACTTCA | 254065 |
rs760865847 | snp | A/G | 2.33438e-05 | 0.00341633 | intron-variant | BRWD3 | GRCh38.p7 | X:80808634 | AAGGGGGAAGCGGAG[A/G]CAAATGATGAAGGAA | 254065 |
rs760875709 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711117 | TCAGTCATATGTGTA[C/T]ATATAATGTGTGTTT | 254065 |
rs760897949 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721923 | GCAATCTTGGCTCAC[C/T]GCAACCTCTGCCTCC | 254065 |
rs760910269 | snp | G/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793080 | GGCAGGAGAATTGCT[G/T]GAACCTGGGAGGCGG | 254065 |
rs760938099 | snp | C/T | 2.39906e-05 | 0.00346334 | intron-variant | BRWD3 | GRCh38.p7 | X:80719468 | ATAAACTACACCCTT[C/T]ACAAGTATAAAAATA | 254065 |
rs760945426 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80682400 | TTATTCATAAACTTT[C/T]ACAAATTAGGTAATA | 254065 |
rs760954388 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730309 | AATAAGTCAAAAAGT[-/G]GAAACAACCCAAATG | 254065 |
rs760958599 | snp | C/T | 3.40913e-05 | 0.0041285 | intron-variant | BRWD3 | GRCh38.p7 | X:80736129 | AATAAAAAGTTTTCA[C/T]GTTCAGCCTAACATC | 254065 |
rs760969213 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80752107 | AGCCAAGACCTCCTG[A/G]GCTCAACTGATCCTC | 254065 |
rs760970378 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754653 | GGTTTATCATACATG[C/T]CCTTTATTATTTTGA | 254065 |
rs760977079 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701498 | AGGTTGCAGTGAGCC[A/G]AGATAGCCCCACTGC | 254065 |
rs760981422 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740255 | TCTCCTCCAAAAGTG[A/G]TCTCTTTCTCCAAAG | 254065 |
rs760989058 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724871 | TATACTTTAATTAAC[C/T]AAGTTATTATATGAG | 254065 |
rs760992486 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711860 | GTCTTACATGTACTG[A/G]TTGATGTCTTGTCTC | 254065 |
rs760998636 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792248 | AGATTAATAAGCTTT[A/G]AAGTTTACATCAGTT | 254065 |
rs761041102 | in-del | -/TTTTTTA | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80774263 | TTTTTATTTTTTTAT[-/TTTTTTA]TTTTTTATTTTTTTT | 254065 |
rs761052536 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671943 | ACTGCCTAATGTGTA[C/T]CTGGTGACATATGCA | 254065 |
rs761053797 | snp | A/G | 2.46752e-05 | 0.00351241 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677355 | TAAGGGGTCCATCAA[A/G]GGAGTGATCTAAATT | 254065 |
rs761055934 | snp | C/T | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80742356 | GTGTGATGCCTCTGG[C/T]TTTGTTCTTTTGGCT | 254065 |
rs761070178 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698602 | TAATCCCAGTTACTC[A/G]AGAGGCTGAGGCAGG | 254065 |
rs761073348 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773580 | CAGCACTAAGCTAAC[G/T]AAGCTAGCTCAGTCC | 254065 |
rs761074900 | snp | C/G | 0.000163474 | 0.00903938 | intron-variant | BRWD3 | GRCh38.p7 | X:80808987 | TCACCTCAACCCTCC[C/G]CACCCTTCCCGAAGG | 254065 |
rs761079042 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698058 | ATTTCCCTAATGATT[-/A]GTGATGTTTTAGCAT | 254065 |
rs761091176 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756963 | TGATGCAAGTCTAGA[C/G]ATGAGCAATTTAACT | 254065 |
rs761093527 | snp | C/T | 2.28146e-05 | 0.0033774 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744186 | ATTTCAGCAGAGTGT[C/T]CACGAAGTGTAGCAA | 254065 |
rs761095443 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732501 | GGTAGGGCATGAACC[A/G]TAAAAGGAAGATAAG | 254065 |
rs761099761 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801507 | AGGCGTGAGCAACCG[A/C]GCCCGGACGAGAAAA | 254065 |
rs761111725 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798981 | GTTTCTCTGCCCACT[C/G]CTCTTTCTACTACTG | 254065 |
rs761154617 | snp | A/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669621 | TGTAAGCTTTTTTTT[A/T]AAAGCCAAGGGAGGA | 254065 |
rs761167707 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734892 | TAGGGGGTCTGTTTT[G/T]TACCAAGCAAAATCA | 254065 |
rs761182153 | snp | A/G | 0.00105904 | 0.0229869 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669478 | ATAAATTAAACGTAC[A/G]GAAATAATTCAGAAC | 254065 |
rs761182499 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80784095 | AATGTCTGTATAACA[C/T]AAAGAAAGGCTAAAT | 254065 |
rs761197554 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809663 | ATTCTAGCCCAAGAG[C/T]TGAGGAGGCGGAGGA | 254065 |
rs761201472 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798144 | AAATATGATTGTAAC[A/G]CTAGAGAAACAGATT | 254065 |
rs761207503 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80680859 | TGTCACACGGGCTGG[A/G]GTGCAGTGGCACAAT | 254065 |
rs761213700 | snp | G/T | 2.33285e-05 | 0.00341522 | intron-variant | BRWD3 | GRCh38.p7 | X:80696691 | TAAAATATACAATAG[G/T]TATTAAAATACACAC | 254065 |
rs761229026 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756451 | AGGTAGCAGTGAGCC[A/G]AGATCGCACCATTGT | 254065 |
rs761233815 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697505 | GGAGTCCCCAATGTC[A/T]ATCATTTCCATCTAC | 254065 |
rs761235446 | in-del | -/CTGCCTCCTCTTCCT | 2.30086e-05 | 0.00339172 | cds-indel, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676943 | CGACTCCCTCGTCCC[-/CTGCCTCCTCTTCCT]CTGCCTCCTCTACTC | 254065 |
rs761240574 | in-del | -/AAAG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730393 | ATTATTTAGCAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 254065 |
rs761256979 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715129 | ACCCTGTCCATTAGT[C/T]TCAGCCAAGTCTGAT | 254065 |
rs761277840 | snp | C/T | 0.000529661 | 0.016265 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692139 | ATCTTTTCTCTCTCA[C/T]TATTGTCCCAGCTAT | 254065 |
rs761290153 | snp | A/C | 2.2853e-05 | 0.00338023 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744244 | TTTTTACTAAACAGT[A/C]ATCTGAACCCTATAG | 254065 |
rs761296571 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798081 | GACTAGGCGACAGAG[C/T]GAGACTCCACCTCAA | 254065 |
rs761320862 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803390 | ACTTTCACAGTATCT[A/C]ATTTGTACTGAGATA | 254065 |
rs761325598 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734976 | CACATTACTTAGAGT[C/T]CAAAAGAGTTTATCT | 254065 |
rs761326415 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80773347 | ATTCCTTTAGCCTTA[C/T]GCCCACCTCTGTCAT | 254065 |
rs761336261 | snp | C/T | 2.33768e-05 | 0.00341875 | intron-variant | BRWD3 | GRCh38.p7 | X:80691798 | TCTCTTGCATGCTCC[C/T]AAAATTTTTTCACAT | 254065 |
rs761350964 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714388 | AGACATGCACCACCA[C/T]ACCTGGCTACCCAAA | 254065 |
rs761355398 | snp | C/T | 0.000335754 | 0.0129524 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745668 | GTGCTGGTAAGCAGA[C/T]GAAGGGAAAATATGA | 254065 |
rs761365522 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80798626 | GTGTATAATACGGGG[A/G]AAAAAAAAAAAGAGT | 254065 |
rs761383038 | snp | G/T | 2.2798e-05 | 0.00337616 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722616 | CTTTACAATTTTCCC[G/T]TCCTGGTACCAACCG | 254065 |
rs761384796 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788371 | TATAAAGAACTCTCA[A/T]AACTCAATAATAAAA | 254065 |
rs761393144 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782893 | CAGAATAAGGCAAGA[C/T]CCTATTTAAAAATAA | 254065 |
rs761393210 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765166 | GCTTCCACCAGGAGA[C/T]ACAACAATAATTCTA | 254065 |
rs761400261 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688582 | GTATCTCTCTAAGGG[A/T]TAATTTTTTAATATG | 254065 |
rs761426961 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746564 | TTGCCCTGTGAAATC[C/T]TTCATCTTCCCTTAT | 254065 |
rs761435879 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734454 | ATGATCATAAACATT[A/T]AAGAACACATCCTGA | 254065 |
rs761436212 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720233 | TGTAAAACAGCCTCA[A/G]GAAGGTCCTCCTGGA | 254065 |
rs761446602 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706505 | TAAAAACTAAGACAC[A/C]AACATTAGCCTAAGC | 254065 |
rs761446825 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766549 | CAACACCAAATGCAG[A/G]CAAGGATGCAGAGAA | 254065 |
rs761484464 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770530 | AATAGATGCAGAAAA[C/G]GCCTTTGACAAAATT | 254065 |
rs761487755 | in-del | -/TAA | 4.65197e-05 | 0.00482262 | intron-variant | BRWD3 | GRCh38.p7 | X:80683998 | GATAATTAACCCAAC[-/TAA]TAATCATACCCTTGA | 254065 |
rs761487816 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774709 | GGGACTAACAGATTA[-/T]TTTTTTATTCTTCCT | 254065 |
rs761489312 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697435 | CCAAATAGTAACCAC[G/T]GTAACAAATAGCTAA | 254065 |
rs761498460 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670514 | TTGACCTCCCAGGCT[C/T]GAGTGATCCTCCCAC | 254065 |
rs761515753 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80778727 | AATTTGGCCAGGCAC[G/T]GTGGCTCACACCTGT | 254065 |
rs761517679 | snp | A/C/T | 4.74358e-05 | 0.00486992 | intron-variant | BRWD3 | GRCh38.p7 | X:80723723 | TCCTAAATTATACTC[A/C/T]ACAGCAAAATTTAAA | 254065 |
rs761551244 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720870 | ATATGCTTAGATATA[C/T]AAATATGTACCATTG | 254065 |
rs761560620 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781502 | TGTCTCTCAGTCCCC[C/G]CTCTCAACAAGAAAA | 254065 |
rs761577290 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80696428 | TCTTTAGGAAGAGAT[A/T]AGCATTTCCATTTTA | 254065 |
rs761590563 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80735501 | ACCAAGATTTTCTAT[A/G]TAAATTGTCTCTTCA | 254065 |
rs761629441 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676358 | GTCTGTGTGTGTGTA[C/T]GTGTGTGTATGTGTT | 254065 |
rs761635985 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80677997 | GCCAGTATAACCAGA[A/G]TGGAATAGAAAAACA | 254065 |
rs761640848 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80804120 | GCATATAAAATGAGG[C/G]TAATACAATCTATGT | 254065 |
rs761641367 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799441 | TACGCTATTTGTTTT[-/C]CAAGACCATGGCTAC | 254065 |
rs761650127 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702528 | TTTACAAGTTCTCTG[-/T]TTTTAAGTATAGCAT | 254065 |
rs761652426 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80692546 | TGCCTAGAATTCATA[C/T]GACTAAACAAAAGAC | 254065 |
rs761657556 | snp | C/T | 7.65628e-05 | 0.00618672 | intron-variant | BRWD3 | GRCh38.p7 | X:80709381 | AATGGATGATACAAA[C/T]TGGGAAACAAAAAAC | 254065 |
rs761680650 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748254 | CACAGGTTTGGTGAT[C/T]TGCCCACCTCGGCCT | 254065 |
rs761682164 | snp | A/G | 3.29603e-05 | 0.00405944 | intron-variant | BRWD3 | GRCh38.p7 | X:80729868 | ACTATTAAACTCAAT[A/G]TAAAATATATCATGA | 254065 |
rs761688276 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80747485 | GTATAAAAGCAAAAA[A/G]CATCATTACCAATAG | 254065 |
rs761698864 | snp | C/G | 2.72554e-05 | 0.00369147 | intron-variant | BRWD3 | GRCh38.p7 | X:80684207 | GTATAGCAATATTAA[C/G]GAATACAATGGGACT | 254065 |
rs761710743 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775244 | CTTTACACAAAAAAT[C/T]TGCAGACTCCTGGCA | 254065 |
rs761732795 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80712959 | TCCGCCCGGCACCCA[A/C]CCCGTCTGGGAAGTG | 254065 |
rs761749266 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712565 | CAGCCTCTGCCCGGC[C/T]GCCACCCTGTCTGGG | 254065 |
rs761759049 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779541 | CAGCCTGGGCAACCC[C/T]GTCTCTACAAAAAAA | 254065 |
rs761761758 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804943 | AATTCTGGAAAATTT[A/C]GAGTGTTATATTTTA | 254065 |
rs761762097 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80771038 | TACCTAGGAATCCAA[C/G]TTATAAGGGATGTGA | 254065 |
rs761763777 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793905 | GAATCAGGCCTGGGC[A/G]CGATGGCTCACGCCT | 254065 |
rs761780188 | snp | A/C | 2.31217e-05 | 0.00340004 | intron-variant | BRWD3 | GRCh38.p7 | X:80691044 | ATAAGTGATTAAAAA[A/C]AAACAGACCTGTAAA | 254065 |
rs761795427 | snp | C/T | 5.54362e-05 | 0.00526451 | intron-variant | BRWD3 | GRCh38.p7 | X:80696014 | AAAATAAAGCACATA[C/T]GAATCAATATAGAGA | 254065 |
rs761806195 | in-del | -/AAA | 0.00529377 | 0.0511748 | intron-variant | BRWD3 | GRCh38.p7 | X:80731895 | GCGAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 254065 |
rs761815673 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80683062 | ATGTAAAATGGATAA[C/T]TGGAAACAACCTAAA | 254065 |
rs761819686 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744480 | TGTGAAGAACTTTTC[A/G]AAATTACCACCAATA | 254065 |
rs761833041 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679223 | ACTAAGGTGATAGCA[A/G]TAGAAACTATATAGA | 254065 |
rs761838716 | in-del | -/AAAT | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80700740 | AAACTCCCTGTCAAA[-/AAAT]AAATAAATAAATAAA | 254065 |
rs761874849 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791080 | AATATTTCTAGCTTC[A/C]ATTTACTTAACCTCT | 254065 |
rs761879695 | in-del | -/TTAAAAG | 0.000111352 | 0.00746082 | intron-variant | BRWD3 | GRCh38.p7 | X:80745759 | AAATTAACTTAAAAC[-/TTAAAAG]TGAAACTGATTTCAT | 254065 |
rs761896299 | snp | A/G | 7.33407e-05 | 0.00605516 | intron-variant | BRWD3 | GRCh38.p7 | X:80719456 | TAATTACAGTACATA[A/G]ACTACACCCTTTACA | 254065 |
rs761897219 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80769067 | TATATATGCACCCAA[C/T]ACAGGAGCACCCAGA | 254065 |
rs761898201 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740159 | GCTCCCCATAAAAAG[A/G]TGATATATTATTTAA | 254065 |
rs761899883 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730901 | ACTACTATCACTTTT[A/G]ATAAGTGTTCAACTA | 254065 |
rs761925563 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768476 | TTTCATATCCAGCCA[A/C]ACTAAGCTTCATAAG | 254065 |
rs761933323 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785679 | ATCTTTAAAGTGAGT[C/T]GCTAAAATCAAGATA | 254065 |
rs761941078 | snp | A/G | 2.27998e-05 | 0.0033763 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717621 | ACTCTTCTGCTCCAC[A/G]CCATGAGATCTCTTT | 254065 |
rs761941331 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787268 | TTAGAAGGCTCAATG[A/C]TGTCAAGATATCAGT | 254065 |
rs761947125 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726114 | CATGTTATGTGTCTG[C/T]ATAACATATAACACG | 254065 |
rs761963615 | snp | A/G | 2.3777e-05 | 0.00344789 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793743 | AATTTTAAGGAGGTA[A/G]TCTGGAGGAATGTGT | 254065 |
rs761968300 | snp | A/G | 2.28326e-05 | 0.00337873 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80693023 | CCCAAACCACCAGGC[A/G]TCATCTATTATACTG | 254065 |
rs761971168 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777207 | CACGACAGAATTTTA[A/C]TCCCAAGAAAGATGA | 254065 |
rs761988611 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729083 | TCTGCATAGGGCAAT[A/G]CCCATTAGCTTATTT | 254065 |
rs761994360 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80738477 | AAAAAAATACAAAAC[A/G]TGGGAGAATAATATA | 254065 |
rs761994597 | snp | C/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677271 | CTCCTCCCATGTTTT[C/T]ATCTTCTTCTGATGC | 254065 |
rs761996438 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705923 | AGAACATTACCGTAC[A/G]CTACTGAAGACTTTA | 254065 |
rs762007522 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694487 | GACAACGTGCGCCGT[A/G]TGCCTGGAAAAGCTG | 254065 |
rs762011378 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776503 | GAAACATTTATAAGA[C/T]TACATGTTAAAGAGT | 254065 |
rs762018167 | snp | A/G | 2.29022e-05 | 0.00338387 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676839 | CATCATCTGCAATAC[A/G]TGCTCGTTTGGCTCT | 254065 |
rs762026893 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811209 | ATATAAAAAGATACA[C/T]GAGACCTAGACAACT | 254065 |
rs762051473 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739823 | AACAATATACTATAA[C/T]AAAAGTTATATGAAT | 254065 |
rs762101905 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697170 | GTAATATATCTATTT[C/T]GGAAAAACTCCCTAG | 254065 |
rs762108287 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673147 | AGTATTAGAAGGCTG[A/T]GTTAAATATCTGAGC | 254065 |
rs762109582 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769174 | CACTGTCAACATTAG[A/T]CAGATCAATGAGACA | 254065 |
rs762109918 | snp | A/T | 2.42615e-05 | 0.00348284 | intron-variant | BRWD3 | GRCh38.p7 | X:80704892 | AGTATAGAAAAGGAG[A/T]AGTTTTACTTAATAA | 254065 |
rs762134118 | snp | C/T | 2.40489e-05 | 0.00346754 | intron-variant | BRWD3 | GRCh38.p7 | X:80735226 | TAAGGTGTTTTTGTG[C/T]TTCATCATGTTTGGC | 254065 |
rs762137129 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718846 | ACTGATAGCTCTTGA[C/T]ACAAGCTAAAACTTA | 254065 |
rs762142496 | in-del | -/AC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782174 | ACATAGGCCAATGGA[-/AC]AGATTAGAGAACTGA | 254065 |
rs762151125 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80752814 | GGATTACAGGTGCCC[A/G]CCACCACACCCAGCT | 254065 |
rs762169552 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808848 | AGTTAAGACCCCAGC[A/G]TTGTCTGCCCCTTTT | 254065 |
rs762204772 | snp | C/T | 8.43668e-05 | 0.00649433 | intron-variant | BRWD3 | GRCh38.p7 | X:80689865 | AGAAACAAGTCATTT[C/T]AAAAGCTTCAGTAAT | 254065 |
rs762211653 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724870 | GTATACTTTAATTAA[A/C]CAAGTTATTATATGA | 254065 |
rs762215495 | in-del | -/A | 0.0605624 | 0.163136 | intron-variant | BRWD3 | GRCh38.p7 | X:80782956 | CAAACAACTCAATAG[-/A]AAAAAAAAAATCTAA | 254065 |
rs762227363 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80761860 | ATCAATAGCAGAATC[C/T]AAATTTAAAGTGCAT | 254065 |
rs762229223 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721876 | ATTGAGACAAGAGTC[A/T]CACTCTGTCGCCCAG | 254065 |
rs762246697 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80690875 | CAGCCTTTCTTCTCT[A/G]TCCCCAAGAGTGAGA | 254065 |
rs762254238 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670160 | AGAACTTTGGGGGAA[A/G]AATCGATACCGTAAA | 254065 |
rs762261928 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751082 | TAGAAAGGTAGTTAC[A/C]ACAGGATACAAGGAA | 254065 |
rs762268932 | snp | A/C | 2.28027e-05 | 0.00337651 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717638 | CATGAGATCTCTTTC[A/C]GTGGCCATCTGGCTC | 254065 |
rs762268989 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80772563 | ATGGCCCATGTATAC[A/G]TATGTAACAAACCTG | 254065 |
rs762283003 | in-del | -/ACAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750857 | ATCAATGTGTTTTAT[-/ACAC]ACACACACACACACA | 254065 |
rs762290547 | snp | A/T | 2.28838e-05 | 0.00338251 | intron-variant | BRWD3 | GRCh38.p7 | X:80688057 | TCCTCAGCAGTTCAC[A/T]TATTTACTCACCTTT | 254065 |
rs762297452 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679985 | GAAAAACAAAGGCAC[A/T]AATTATTTTCAAGTA | 254065 |
rs762338681 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767827 | AAGGAAGCTAAAAAC[A/T]TTGAAAAAAGATTAA | 254065 |
rs762361526 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80764668 | CCATAAAAGGGAAAA[C/T]TGGTAAACAGGGTGT | 254065 |
rs762364498 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714052 | AAAGTTGTCTCTTGT[C/G]GGGGAAAACCTACAT | 254065 |
rs762388792 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80719767 | AAAAACAGCATTAAA[C/T]GTAAAATAAAGTATA | 254065 |
rs762409611 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80701405 | ATACAAAAATTCACC[A/G]GGCGTGGTGGTGCAC | 254065 |
rs762412732 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807743 | CTTTGGTCCTTCACT[A/G]AAGTATATTCCATTT | 254065 |
rs762428711 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689364 | ATTTCATGAAACTAC[C/T]AAAAATTTAGACTTT | 254065 |
rs762444851 | snp | A/T | 2.3337e-05 | 0.00341584 | intron-variant | BRWD3 | GRCh38.p7 | X:80691034 | AAATTTTATAATAAG[A/T]GATTAAAAAAAAACA | 254065 |
rs762458769 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731609 | ATCCTATAAAGTCCT[C/T]ATAGGCCGGGCGCAG | 254065 |
rs762459122 | snp | A/G | 2.58348e-05 | 0.00359398 | intron-variant | BRWD3 | GRCh38.p7 | X:80689946 | AAGTTAGACTCTCTG[A/G]AAGCTAAAACTGCTT | 254065 |
rs762463133 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771998 | GATGTGGAAAAATAG[A/G]AACGCTTTTACACTG | 254065 |
rs762470311 | snp | A/C | 2.28063e-05 | 0.00337678 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677111 | TCATGGTCTCCATCT[A/C]CGTAATCTTGATCTG | 254065 |
rs762475206 | in-del | -/AG | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809739 | AGAGAGAGAGAGAAG[-/AG]AGAGAGAGAGAGAGG | 254065 |
rs762490248 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729433 | AGAAGCTGTAGTGTC[C/T]CAAAGAGGTAATTAT | 254065 |
rs762511118 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708895 | TTAAACCTTCATTAT[A/G]CATTTAACAATGAAA | 254065 |
rs762511697 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779459 | GTGGCCAGGTGGAGC[A/G]GTTCATGCCTGTAAT | 254065 |
rs762515347 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80713564 | ACTGCGGAAGGCCGC[A/G]GGGTCCTCTGCCTAG | 254065 |
rs762524485 | in-del | -/TTTACATGTTATATGTCTGTATA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726230 | ATAACATATAACACG[-/TTTACATGTTATATGTCTGTATA]ACATATAACACGTTT | 254065 |
rs762528498 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698844 | GTAAAGCTCACTTGA[-/T]TAAGCTACTTTAGCA | 254065 |
rs762533670 | snp | C/T | 6.02991e-05 | 0.00549053 | intron-variant | BRWD3 | GRCh38.p7 | X:80743992 | GAGAATTCTCACCTT[C/T]TTTACATATGTTCAA | 254065 |
rs762538084 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80679164 | CACCCAGTCTGTGGT[A/G]TCTTGTTATGGAAAC | 254065 |
rs762543761 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803009 | CAGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 254065 |
rs762558692 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80741025 | TTAACTCATCATTTA[A/G]CATTAGGTATATCTC | 254065 |
rs762561387 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726152 | ATGTCTGTATAACAT[A/G]TAACACGTTTACATG | 254065 |
rs762565086 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763553 | TCACAAGAAACAAGA[C/G]CAATACACAAAACTC | 254065 |
rs762583192 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775233 | ACTATCTGGCCCTTT[-/AC]ACAAAAAATTTGCAG | 254065 |
rs762595734 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787520 | CACGATAATCCAATG[C/G]GGAAAAGGATGGCCT | 254065 |
rs762617252 | in-del | -/CA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715445 | GACTCTTCAAATTAC[-/CA]CACTCTACAGAAATT | 254065 |
rs762620645 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778598 | CATCTTCAAATACAA[A/G]GAGTTTTTCAGAAAA | 254065 |
rs762646944 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757224 | TATCCCAGGCTCTAT[C/T]TACTAAAAAATTTAA | 254065 |
rs762653125 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80791261 | AGTAATGGAGCAGAG[A/G]AGCAATTACTCACCC | 254065 |
rs762657695 | snp | A/C | 2.28227e-05 | 0.00337799 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744210 | GTAGCAAGAAGGCGT[A/C]CATCATCTGTAGCCC | 254065 |
rs762665194 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80706463 | ATTTTTAAGGTTTAA[A/C]ATTTTTTTTTATTTT | 254065 |
rs762668574 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746290 | CTAGGTTTGTCTATG[G/T]GTTCTTTCCTTTTGG | 254065 |
rs762686713 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80726343 | ATGTTTACATGTTAT[A/G]TCTGTATAACATATA | 254065 |
rs762706480 | in-del | -/AGAAG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740312 | TTGCTCTCAACAGAA[-/AGAAG]AGGACAAAAGCTCAT | 254065 |
rs762711880 | snp | C/T | 5.65867e-05 | 0.00531885 | intron-variant | BRWD3 | GRCh38.p7 | X:80677414 | TTGACATTGACAAAA[C/T]GGTTATTTAGGTTCA | 254065 |
rs762720229 | in-del | -/A | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80742159 | CCAGCACCATTTATT[-/A]AATAGGGAATCCTTT | 254065 |
rs762721298 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796939 | AGTACTTTGGGAGGC[C/T]GAGGAGGGAGGGTTG | 254065 |
rs762749550 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80769793 | ACCTTCAAAAAAAAA[A/G]AATCAATGAATCCAG | 254065 |
rs762751511 | snp | G/T | 4.66418e-05 | 0.00482895 | intron-variant | BRWD3 | GRCh38.p7 | X:80728955 | AAATTTTTGACAAAG[G/T]TGCATGTTAAATAGC | 254065 |
rs762774352 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746374 | TCTCCTATGAAGTCA[C/T]TTTAAGTCCTATCTC | 254065 |
rs762781290 | snp | A/C | 9.08306e-05 | 0.00673848 | intron-variant | BRWD3 | GRCh38.p7 | X:80728739 | TTAATTACTCTAAAA[A/C]TAAAATACTTACAGA | 254065 |
rs762786237 | in-del | -/TAAT | 2.47268e-05 | 0.00351607 | intron-variant | BRWD3 | GRCh38.p7 | X:80719441 | TTGGTAAAAGTAAAA[-/TAAT]TACAGTACATAAACT | 254065 |
rs762787889 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711999 | AATAAATCTCTTCAA[A/G]TATTTTATAGAGTTT | 254065 |
rs762823238 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764875 | GGCATAGACACTTCA[C/T]CAAAAAGGATATACA | 254065 |
rs762827136 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695976 | AAGTCAATGACATCC[A/G]GCATGTCATGATACC | 254065 |
rs762827701 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80697249 | TATGTAAGCATCCAG[A/G]TATATATGTACGTGT | 254065 |
rs762835008 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756339 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAATT | 254065 |
rs762855809 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793033 | TGGGCGAGGTGGCAC[A/G]CGCCTGTAGTCCCAG | 254065 |
rs762857510 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80696337 | CTATTATTATTAACA[A/G]AAATAAAAGCAACCA | 254065 |
rs762860736 | snp | C/T | 2.28115e-05 | 0.00337716 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682517 | TTCTTAGACGTTTTC[C/T]GTACCGTGGCCTTCT | 254065 |
rs762867809 | snp | C/G | 6.85432e-05 | 0.00585379 | missense, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793644 | ATCCCGTAGCAGAGA[C/G]TGCCGACCAACACCT | 254065 |
rs762886663 | snp | C/T | 2.27905e-05 | 0.00337561 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677027 | CCTCTGGTCTTCCAA[C/T]TTCTTTTTCCATTGC | 254065 |
rs762890746 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702292 | TCTTGAAGCATATAA[A/G]GATGTAGTAAGTTTA | 254065 |
rs762892571 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804044 | ATATTTTTTAAGGAC[-/A]ATAACAAACAATCTT | 254065 |
rs762898304 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779360 | GCAATCCTCTGATTG[A/G]TTAAAGTGTAGTAAG | 254065 |
rs762910264 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685719 | AAAAACACAAGACTA[A/T]TTTATTTTACCCAAA | 254065 |
rs762937453 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80720856 | CCTTTTCTGTCTAGA[C/T]ATGCTTAGATATACA | 254065 |
rs762954944 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685736 | TTATTTTACCCAAAT[C/T]CCCTACAAGCAAACA | 254065 |
rs763007623 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735196 | ATTTCACCGGGCGAT[A/C]TCTAAAGATAAAAAT | 254065 |
rs763010501 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80753920 | TGCTGTTTTGGTTAC[C/T]AGAACCTTGCAATGT | 254065 |
rs763022425 | snp | A/G | 5.80931e-05 | 0.00538917 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791873 | ATTTGGAGGTTTCAC[A/G]TAATTTACAGGTAGT | 254065 |
rs763030683 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753100 | TGTATATTTTGGTTA[C/T]TAGTCCCCTATCAGA | 254065 |
rs763032254 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80800353 | AAGACCAGCCTGGGC[-/A]AAAAAAAGTGAGATC | 254065 |
rs763036239 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80776368 | ATGAAACTTCAAACC[A/G]ATGTCAGAAAAATGT | 254065 |
rs763037447 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725824 | TTACATGCCTATATA[A/G]CATAACATGTTTACA | 254065 |
rs763057760 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80774908 | TCTCTCCTCTCCAGT[C/T]TATCATATACTCTAC | 254065 |
rs763068817 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774841 | CATTCATTTTCTGTC[A/T]ATATCTATAGTAACA | 254065 |
rs763070938 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757576 | TAAATTAGTCAAATA[C/T]AGATTTGAATACAAT | 254065 |
rs763085722 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725975 | CATAACATGTTTACA[C/T]GTTATATGTCTATAT | 254065 |
rs763096478 | snp | G/T | 2.28577e-05 | 0.00338058 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716224 | ATTTCTATGTCACCT[G/T]TTGCAGTTCGACATT | 254065 |
rs763101313 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687103 | ATCTGTATGTGTGTA[-/TA]TATATATATATATAT | 254065 |
rs763107045 | in-del | -/AGAG | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809737 | AGAGAGAGAGAGAGA[-/AGAG]AGAGAGAGAGAGAGG | 254065 |
rs763109654 | in-del | -/CAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693324 | TTTTCAATTAATTAG[-/CAT]CATCATTAGGCACAC | 254065 |
rs763124144 | snp | A/C/T | 6.84476e-05 | 0.00584978 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692997 | TGAAAAGGCTGCTGA[A/C/T]TCTCCACAGTCCCAA | 254065 |
rs763128944 | snp | C/T | 2.28626e-05 | 0.00338095 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676812 | AACGTCCTGAAAACA[C/T]GGTATCAAATTCATC | 254065 |
rs763129532 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725973 | CACATAACATGTTTA[C/T]ATGTTATATGTCTAT | 254065 |
rs763169324 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728294 | CTTTTTACATAACAA[A/C]TACTACAGCCTCTTA | 254065 |
rs763172862 | in-del | -/AACA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680420 | CTCCTTATATGAAAT[-/AACA]AACAGAACTGTCTGG | 254065 |
rs763173179 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80692524 | CCAAACATGATGCAA[C/T]CACCTCTGCCTAGAA | 254065 |
rs763200476 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80699285 | GTCAAGAATCATCAC[A/C]CAACTCTTCATTTAC | 254065 |
rs763209948 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810935 | ATTGAAATATTACAA[A/T]TTGAAGGTTCATCTA | 254065 |
rs763220078 | snp | A/G | 2.30465e-05 | 0.00339451 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686959 | TTGTTTTTTCCAAGC[A/G]TCAGGATTACACTTT | 254065 |
rs763255761 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682832 | ATGTTCTAAAAGGTA[C/G]GGAAAAAAAGACTCT | 254065 |
rs763264620 | in-del | -/T | 0.00106213 | 0.0230204 | intron-variant | BRWD3 | GRCh38.p7 | X:80693392 | ATTCTTCTATCTTGC[-/T]TTTTAGCTTTCTTTA | 254065 |
rs763271232 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767646 | AAACCAGAGAGAAAA[C/T]TATAAAAACCAGAGA | 254065 |
rs763281992 | snp | C/T | 1.97198e-05 | 0.00313998 | intron-variant | BRWD3 | GRCh38.p7 | X:80809430 | CCCCACCCCCCGACA[C/T]AGCTACCCACCGGCT | 254065 |
rs763291927 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785581 | ACTCCAACATAGTGC[A/T]AAGTCCAGATAAGGT | 254065 |
rs763297487 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80790114 | CGCTTGAACGAGGGA[C/G]TGGGGAGGTTGCAGT | 254065 |
rs763301809 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772929 | AGGAATGAATACTGA[C/T]ACTTGCAACAAATAA | 254065 |
rs763316217 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693375 | TGTACATAAATGCAG[C/T]TGATTCTTCTATCTT | 254065 |
rs763318710 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737487 | AGATGCAGAATCTAC[A/G]GATACAAAGGGTAAA | 254065 |
rs763336751 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716619 | TCTTTTGCTTAGCAT[A/G]TTTATCCACGTTGTA | 254065 |
rs763361602 | snp | G/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677318 | TTGATTCCTGTCCGG[G/T]GCTCTCTGCCATCAC | 254065 |
rs763383271 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80700410 | CATCAACAAATCCAA[A/T]CAACTGCAGATTGAA | 254065 |
rs763393081 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759439 | AGGCTTTAATTAATT[C/T]GGGCCTCTTAAAGCA | 254065 |
rs763396242 | in-del | -/TCTT | 5.42241e-05 | 0.00520664 | intron-variant | BRWD3 | GRCh38.p7 | X:80809230 | CACGACTCCCAGATC[-/TCTT]TCTTCCCCTTACCTG | 254065 |
rs763401592 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806353 | AGCCTCACTAGTAAT[A/G]AAAAAAAAAGAGCTA | 254065 |
rs763407847 | snp | A/C | 3.4283e-05 | 0.00414009 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704632 | AAGTTATCAAAGGCA[A/C]AAAACAAAAAATAAC | 254065 |
rs763415958 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671487 | AACTCCATATTTCTT[C/T]CTTCTGGTTAATTTT | 254065 |
rs763422245 | snp | A/G | 6.22394e-05 | 0.00557816 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703542 | CCAAGATCCACTGAG[A/G]GGCAAACCATTCTTC | 254065 |
rs763443134 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80801030 | GGACCCACCCACATT[C/T]TAGTAGGTGCTCAGT | 254065 |
rs763451342 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80688379 | AAGGAGGGGAACAGT[G/T]TAGTGGTTGGTATTT | 254065 |
rs763456346 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807865 | CGGGTCTATGCAAAT[A/G]CGACTTAACTGATAA | 254065 |
rs763456771 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783441 | TGCTGGTGAGGTTTT[A/G]GAGAAAAGGGAACCC | 254065 |
rs763474970 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699770 | ATAGAAAATAGCATA[C/T]AAATTTTGAGAAACG | 254065 |
rs763478529 | snp | C/T | 2.30577e-05 | 0.00339534 | intron-variant | BRWD3 | GRCh38.p7 | X:80681294 | TGATTTATCTGCTAT[C/T]ATAAAGAAATAAATA | 254065 |
rs763490986 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763633 | AACAAAATCTATTTA[C/T]GATCACGCCAAAGAA | 254065 |
rs763494121 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737790 | CAGTTAGCTGAGACC[A/G]TACCACCGCACTCCA | 254065 |
rs763509206 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710424 | TCAGTCAGCTCGTAC[A/T]TACTTGGAGAGACAT | 254065 |
rs763516668 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679142 | GATGAATGTCTGCTG[C/T]TTAAGCCACCCAGTC | 254065 |
rs763528817 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722949 | TAGAAGAGAATTGAA[C/T]TACCTAAATGGTAAT | 254065 |
rs763538702 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80806705 | TTGGTTCAAATCATA[C/T]CGTACCTTAAATACA | 254065 |
rs763568028 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749875 | ATAGAAACAGCATGA[C/T]ACTGACGTAGAAACA | 254065 |
rs763580276 | snp | C/T | 4.56835e-05 | 0.00477909 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728884 | TTTAGTGATCTTGTC[C/T]TCTCCAGATGGCAAA | 254065 |
rs763607873 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80760479 | AATGCTAATGAATTA[C/G]CTTTAGAAATTAAGA | 254065 |
rs763631063 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679911 | AGGAAGGGTAAAATG[-/A]AAAAAAGGCAATGGC | 254065 |
rs763634402 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80705640 | CTACACAGCTATTCT[A/G]TATAGGTAGAACCTA | 254065 |
rs763634884 | in-del | -/GGTGATCCTTCCACCTC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706344 | GAACTCCTGACCTCA[-/GGTGATCCTTCCACCTC]GGCCTCCAAAAGTGC | 254065 |
rs763645184 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777603 | AGGGTCTCACCACGC[C/T]GCCCAGGCTAGTCTC | 254065 |
rs763652797 | snp | C/T | 2.95928e-05 | 0.0038465 | intron-variant | BRWD3 | GRCh38.p7 | X:80744001 | CACCTTTTTTACATA[C/T]GTTCAAGCTAAATTT | 254065 |
rs763660186 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733294 | CTACTTGGATGAGAT[C/T]GTGGAAGTGATGGCT | 254065 |
rs763667559 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731975 | TTCTAAAATCTGAAA[C/G]TGTTTTGAGTGTCAA | 254065 |
rs763673567 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766030 | AGACTGGGTCACAGA[A/G]TGCCCAAACATTTGG | 254065 |
rs763677164 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781420 | GCCCCTTGTTTAAAG[C/G]TGGATGTGGTCACCT | 254065 |
rs763695000 | in-del | -/ATGTT | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80726165 | ATATAACACGTTTAC[-/ATGTT]ATATGTCTGTATAAC | 254065 |
rs763696529 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764727 | AAAGCCCATGTGAAA[A/C]GAATGAAAAGACAGA | 254065 |
rs763722199 | snp | C/T | 0.0555816 | 0.157167 | intron-variant | BRWD3 | GRCh38.p7 | X:80713568 | CGGAAGGCCGCAGGG[C/T]CCTCTGCCTAGGAAA | 254065 |
rs763723219 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741439 | CAGTAATGGGATGGC[G/T]GGGTCAAATGGTATT | 254065 |
rs763726740 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790337 | CAAATCACAAACTGG[-/A]AAGATTTCATATCCA | 254065 |
rs763743666 | snp | G/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809814 | GAGAGACGCGGGGGG[G/T]GGGGGGGCGGAGAGA | 254065 |
rs763747441 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80685725 | ACAAGACTAATTTAT[G/T]TTACCCAAATTCCCT | 254065 |
rs763763939 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729585 | GATGACATTTAATAG[A/G]GACAACTCTCAAGGT | 254065 |
rs763792478 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711230 | ATTCTAGATTAACAT[C/T]GAGGGCTAAACTCTG | 254065 |
rs763822630 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708987 | TTATTCATTACCATG[A/G]AAAAGGTAGGTCTGA | 254065 |
rs763826401 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80755322 | CACCCAAAAGATGAT[C/T]TGGTAAAAAAAAGTT | 254065 |
rs763831205 | snp | C/T | 2.28251e-05 | 0.00337817 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722589 | ATCCCAGCTGTGGTA[C/T]AAGCTGTTCATCTTT | 254065 |
rs763832909 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788302 | GGAGGGGAGGAGACA[A/G]CTGCACATTGAGAGA | 254065 |
rs763847217 | snp | C/T | 6.84736e-05 | 0.00585082 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744214 | CAAGAAGGCGTCCAT[C/T]ATCTGTAGCCCAAAT | 254065 |
rs763849446 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80787538 | AAAAGGATGGCCTTT[A/T]CAACAAATGATACTG | 254065 |
rs763867350 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694902 | GTTAAGACTTTGGGG[A/G]ACTGTTGATTGGTTT | 254065 |
rs763870852 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724328 | TAAAGCATATAAAAG[A/T]AAACTCAAAGAGCAA | 254065 |
rs763900465 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80706465 | TTTTAAGGTTTAAAA[-/T]TTTTTTTTATTTTAA | 254065 |
rs763906757 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779499 | TTGGGAAGCAAAGCA[A/G]ATCGCTTGAGGTCAG | 254065 |
rs763923879 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80699595 | TCTTGTGATTTATCA[A/T]ATTTAAAATATACCA | 254065 |
rs763933804 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801214 | GCATGAGAAAACATC[-/T]TTTTTTTTTTTTTTT | 254065 |
rs763945697 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80747398 | CCCCCCACACTAAGT[C/T]GTGACAAACAAAAAT | 254065 |
rs763948933 | in-del | -/CTC | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80720189 | TCATTTTGAAATGTA[-/CTC]CTTTTAATTATTAAA | 254065 |
rs763952586 | snp | A/G | 2.47592e-05 | 0.00351838 | intron-variant | BRWD3 | GRCh38.p7 | X:80689958 | CTGGAAGCTAAAACT[A/G]CTTCTTACCCAATAA | 254065 |
rs763952723 | snp | A/T | 3.29881e-05 | 0.00406115 | intron-variant | BRWD3 | GRCh38.p7 | X:80707540 | TAAGATATATGGATA[A/T]TACCAGCTAATGTAT | 254065 |
rs763958921 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762196 | GTTTACAAGCAAACA[A/T]GTTTTGCCTTTCTCT | 254065 |
rs763961902 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738631 | CACAGTGGAGGGGGT[G/T]GGGGGGGCAGTGGTT | 254065 |
rs763962702 | snp | C/T | 0.00434781 | 0.046422 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676332 | GTCTGTGTTGTGTTT[C/T]GTGTGTGTGTGTCTG | 254065 |
rs763998112 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778654 | TAAAATAACCTTGGA[G/T]TCGTATTTTCTCTTT | 254065 |
rs764007031 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771788 | GAAAAACAAACAACC[C/T]TATCAAAAAGCGGGC | 254065 |
rs764040431 | snp | C/T | 2.51645e-05 | 0.00354706 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707439 | TACCTGGAAGAACTT[C/T]CACTTTGCCATTCAA | 254065 |
rs764051723 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746380 | ATGAAGTCATTTTAA[A/G]TCCTATCTCATTTTT | 254065 |
rs764079513 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804075 | ATAAAAGTTTTTCAT[-/A]AAAAAACATAAAATT | 254065 |
rs764083753 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675089 | GTAAGTATCTAACAA[A/G]TGAACAAATCTGTAA | 254065 |
rs764096423 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80686382 | CGTATGTAACAAACC[C/T]GCACGTTGTGCACAT | 254065 |
rs764099200 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766630 | CTTAAAACACAAAAC[-/AT]GTGGATTCTGTTCCA | 254065 |
rs764106340 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746347 | AGTTAACAATGAACT[A/T]TAAAGGCTTCATCTC | 254065 |
rs764119663 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769799 | AAAAAAAAAAAATCA[A/G]TGAATCCAGGAGCTG | 254065 |
rs764124945 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744415 | AGCAAGTATAAATGA[C/T]GTCCAAATGATAGCA | 254065 |
rs764126621 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80775019 | AATAGGATAAAATCT[-/A]AACTCATTATTCATG | 254065 |
rs764132288 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80791416 | ATAATTTGAATGAGA[C/T]GTGAATTTCATTAAA | 254065 |
rs764144550 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80712001 | TAAATCTCTTCAAAT[A/G]TTTTATAGAGTTTGA | 254065 |
rs764149058 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753961 | AGGTAACATGATGTC[C/T]CCAGCTTTGTTCTTT | 254065 |
rs764162809 | in-del | -/ACACA | 2.38447e-05 | 0.00345279 | intron-variant | BRWD3 | GRCh38.p7 | X:80723702 | CAAAATTTGTGAATG[-/ACACA]ATCCTAAATTATACT | 254065 |
rs764190366 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806399 | AGCTATTGCCATCTA[C/T]TAAATATTAAAGAAA | 254065 |
rs764214716 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80743566 | TTAATTATTGCCTCA[A/C]TTTCCGAGCCTGTTA | 254065 |
rs764218578 | snp | A/T | 2.28537e-05 | 0.00338029 | missense, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793654 | AGAGACTGCCGACCA[A/T]CACCTAATAATGTCT | 254065 |
rs764224302 | snp | A/G | 4.56121e-05 | 0.00477535 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677113 | ATGGTCTCCATCTAC[A/G]TAATCTTGATCTGTT | 254065 |
rs764237646 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735261 | GGGCCAGAATGTTAG[C/T]GCACTACTGGATACT | 254065 |
rs764239936 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758766 | CTCCATCCTGGGCAA[C/T]ATAGCGAGATCCCAT | 254065 |
rs764248043 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682154 | TAGCAACATATTATG[A/G]TAGACAGTATGATAC | 254065 |
rs764292996 | snp | A/G | 0.00581083 | 0.0535878 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809857 | GAGATAGACGGAGCG[A/G]GAAGAGGGAGGAGCC | 254065 |
rs764307057 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702800 | GTTCCTTCTGCTGTT[A/G]CAATGACAATATTAC | 254065 |
rs764318515 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791005 | CTTCAGAGTATCCAA[C/T]TTCCCTGAATAAGTC | 254065 |
rs764348723 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80790226 | AAAAAAAAGATATAC[C/T]TTCATGATTAAATTT | 254065 |
rs764349135 | snp | A/T | 2.29716e-05 | 0.00338899 | intron-variant | BRWD3 | GRCh38.p7 | X:80728917 | ATTGCTAAACAAAAC[A/T]ATTTGCAGTATTCAT | 254065 |
rs764350329 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758607 | ACTTTATCTCTCTCT[C/G]TGTAATTTCCAGAGA | 254065 |
rs764350439 | snp | A/G | 2.28157e-05 | 0.00337747 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682523 | GACGTTTTCTGTACC[A/G]TGGCCTTCTCCTCTT | 254065 |
rs764361084 | snp | A/G | 2.31803e-05 | 0.00340436 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80725035 | TTGATCAAATGGATG[A/G]GCTTCTAGAACGAAT | 254065 |
rs764382676 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699842 | GATCATCATCTTATC[C/T]TGGATACACAATCAA | 254065 |
rs764383400 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776404 | GGCTAAAATAAAGGA[-/T]TTTCAACTCAACAGA | 254065 |
rs764393508 | snp | A/T | 0.000115652 | 0.00760346 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791875 | TTGGAGGTTTCACAT[A/T]ATTTACAGGTAGTTC | 254065 |
rs764394479 | snp | A/C | 0.000179598 | 0.00947452 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809457 | GGCTTCGATCTGGGT[A/C]GGTGCTGCCGCCATC | 254065 |
rs764401280 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768384 | AACAGCGGATCTCTC[A/C]GCAAAAACTCTACAA | 254065 |
rs764422170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80717419 | GATCATTATTTGTTA[C/T]GAAGTGAACTCACTG | 254065 |
rs764438594 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800408 | TTAGCCAGACATGAC[A/G/T]GTGCATGCCTGTAGT | 254065 |
rs764447426 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741059 | CTGCTATCCATCCCC[C/G]CTCCCCCACCCCACA | 254065 |
rs764461771 | snp | C/T | 2.28788e-05 | 0.00338214 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676836 | ATTCATCATCTGCAA[C/T]ACGTGCTCGTTTGGC | 254065 |
rs764470800 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757768 | ATAGATTTACTGTAT[A/G]TATTTTACAAATTTA | 254065 |
rs764479181 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80682834 | TTCTAAAAGGTAGGG[-/A]AAAAAAAGACTCTGA | 254065 |
rs764502517 | snp | A/G | 2.28605e-05 | 0.00338079 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716227 | TCTATGTCACCTTTT[A/G]CAGTTCGACATTCTT | 254065 |
rs764504049 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80722000 | TACAGCCGTGCACCA[A/C]CACCCCCAGCTAATT | 254065 |
rs764522606 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80728321 | CTTACAATGACAAAT[A/G]CACTTTCTGAAAGAG | 254065 |
rs764529385 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783484 | GGTGGAAATGTACAT[C/G]AGTATAGCCACTATG | 254065 |
rs764542130 | in-del | -/G | 5.9453e-05 | 0.00545188 | intron-variant | BRWD3 | GRCh38.p7 | X:80809314 | CAGCTCTGGGGAAGA[-/G]GGGGGGAAAAGAGGT | 254065 |
rs764551317 | in-del | -/AT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795393 | TACACACATATATAC[-/AT]ATATGTGTGTATATT | 254065 |
rs764560427 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689421 | ATATTTTCTATACAG[-/C]ATATAGAAAATAAAA | 254065 |
rs764570489 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80772001 | GTGGAAAAATAGGAA[C/T]GCTTTTACACTGTTG | 254065 |
rs764572560 | snp | C/T | 2.36122e-05 | 0.00343592 | intron-variant | BRWD3 | GRCh38.p7 | X:80735205 | GGCGATCTCTAAAGA[C/T]AAAAATAAGGTGTTT | 254065 |
rs764579901 | snp | A/C | 6.93121e-05 | 0.00588653 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686969 | CAAGCATCAGGATTA[A/C]ACTTTAAAGACTGTC | 254065 |
rs764586925 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782134 | TTGTATCCAAAAACA[G/T]TATGGTACTGGCATA | 254065 |
rs764587615 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673077 | ATTGTCTGATGACAA[A/T]CTATGGGATTAAAAC | 254065 |
rs764590952 | snp | A/G | 2.28266e-05 | 0.00337828 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734193 | AATCACATGGTCAGT[A/G]CTACCAGTTGTAATG | 254065 |
rs764627978 | in-del | -/AAAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788098 | CAAAAATAAATAAAT[-/AAAT]AAATAAATAAATAAA | 254065 |
rs764643263 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807755 | ACTAAAGTATATTCC[A/G]TTTTTAAATATGTCC | 254065 |
rs764646634 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737927 | TGCCTGCTTCTGTAA[A/G]TATAGTGTTATTGGA | 254065 |
rs764652369 | snp | C/G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785591 | AGTGCAAAGTCCAGA[C/G/T]AAGGTCAGAATTTTA | 254065 |
rs764677917 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777534 | AGTAGCTGGGACTAT[A/G]GGCACACAGCACCAC | 254065 |
rs764679530 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795702 | CCTGGGCAACATAGC[A/G]AGATCTCATCCCTAC | 254065 |
rs764708963 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740960 | ACATGTGCACAACAT[G/T]CAGGTTTGTTACATA | 254065 |
rs764738948 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80764604 | AGGTGTGAGCCACCG[C/T]GCCCAGCCTTAGGCA | 254065 |
rs764739037 | snp | C/G | 2.28277e-05 | 0.00337836 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677156 | TCAGAGTCAGAGTCA[C/G]AACCACAGGTACTTT | 254065 |
rs764756596 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688298 | CTTTCCCAATATGCA[A/G]TGTACAAGCTGGAAA | 254065 |
rs764769456 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80806515 | CAATATATGACAAGA[C/G]CTATAAAACTCATGA | 254065 |
rs764769730 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786525 | ATTTGCCTATATATA[A/T]ATATATATGGAGTCT | 254065 |
rs764797632 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80740639 | CGGTAGTACCAGCTA[C/T]TCAGGAGGTGGAGGT | 254065 |
rs764800223 | snp | A/G | 2.42075e-05 | 0.00347896 | intron-variant | BRWD3 | GRCh38.p7 | X:80735235 | TTTGTGTTTCATCAT[A/G]TTTGGCTAATGGGCC | 254065 |
rs764801015 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713326 | TAGACATGGGAGACT[G/T]TTCGTTTTGTTCTGT | 254065 |
rs764816310 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80678465 | ATCCAAGACAAGACA[-/T]TTTTTTTAAAAAAAA | 254065 |
rs764825001 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80771945 | ACCAGTTAGAATGGC[A/G]ATCATTAATAAGTCA | 254065 |
rs764834462 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729086 | GCATAGGGCAATACC[A/C]ATTAGCTTATTTCAG | 254065 |
rs764839300 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799245 | TCATCATAATTAGTT[A/C]AAAGAAATCCAGCTG | 254065 |
rs764848154 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771228 | CTACCAATAACTTTC[G/T]TCACAGAATTGGAAA | 254065 |
rs764849328 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80713553 | GGGACACAAACACTG[C/T]GGAAGGCCGCAGGGT | 254065 |
rs764849926 | snp | A/C | 2.29468e-05 | 0.00338717 | intron-variant | BRWD3 | GRCh38.p7 | X:80688134 | CTGTATCCTTAATTA[A/C]AAAGGAAGAGTGGGA | 254065 |
rs764853232 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721840 | TACCTCCAGCTGCGG[C/G]GTAGGGGTTGTTTTC | 254065 |
rs764853596 | in-del | -/AAC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795592 | ACCAGGTCAATCAAG[-/AAC]AATAGGCTGGGAACG | 254065 |
rs764857424 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805286 | AATGTTGAAGAAATT[A/C]AATTTATCATTACCT | 254065 |
rs764872325 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749851 | AAAATGTATGATAAA[C/G]CTTATTTAATAGAAA | 254065 |
rs764888008 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708747 | CTTGAACCCAGGAGG[C/T]AGAGGTTGCAGTGAG | 254065 |
rs764924574 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754331 | GGTGTACAGAAATGC[C/T]ACTAATTTTTGTACT | 254065 |
rs764925622 | snp | C/G | 0.000118504 | 0.00769664 | intron-variant | BRWD3 | GRCh38.p7 | X:80736130 | ATAAAAAGTTTTCAT[C/G]TTCAGCCTAACATCA | 254065 |
rs764935534 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80717994 | TAATTTTTTTCAAAG[C/T]AGTTTCACATCTGAC | 254065 |
rs764949045 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796868 | GTCAATGCAGCTGAT[A/G]ATTCAATCTAAAAAA | 254065 |
rs764955772 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80726027 | ATATGTCTATATAAC[A/G]TATAACATGTTTACA | 254065 |
rs764958661 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80694610 | CACCTCTTGCATCAG[C/T]GTGACCTGGATATGA | 254065 |
rs764965118 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776943 | TTACAAAAAGTACTT[C/G]CCTCATCCCTCTTAT | 254065 |
rs764973145 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80705499 | AATAAATACATATAC[A/G]GTCATATACAGTCAT | 254065 |
rs764986923 | snp | C/G | 3.0479e-05 | 0.00390366 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80791855 | GGTATATTACTCACC[C/G]ACATTTGGAGGTTTC | 254065 |
rs764992062 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727614 | ATAACAATAAAATAT[C/T]AGATAGTGATAAACC | 254065 |
rs765031513 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734037 | TTTGTATATGTTACT[A/G]TGGTACAGATCAGAA | 254065 |
rs765036770 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787456 | ACTCAGACAGCAGAG[G/T]CCAGAAAGACTCATA | 254065 |
rs765047376 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679057 | ATATAGAAGCCAGGG[-/A]AAAAGCCCTTATCAG | 254065 |
rs765060478 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802911 | GAGATCGAGACCATC[C/T]TGGCTAACACGGAGA | 254065 |
rs765063661 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685385 | CAGTCCTTACAAACT[A/G]TAAGATTCATGTACA | 254065 |
rs765077352 | in-del | -/AT | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80726135 | ATATAACACGTTTAC[-/AT]ATGTCTGTATAACAT | 254065 |
rs765096588 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761433 | TGAAACACACTGAAG[C/T]AATTATATGACAGGC | 254065 |
rs765143959 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769229 | ACTGAACTCAGCTCT[A/G]CAACAAGCAGACCTA | 254065 |
rs765153776 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788583 | TTCGGCAGTTTCTTA[G/T]AAAGTTAAAGTTGTA | 254065 |
rs765159126 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779277 | TCGAGATTGTGCCAC[G/T]GCACTCCAGCCTGGG | 254065 |
rs765169545 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673316 | AAAGGGAAATAAAAA[G/T]AATAGAGGGACACAG | 254065 |
rs765173436 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80737911 | ACCAAATTCAGCTTA[C/T]TGCCTGCTTCTGTAA | 254065 |
rs765175433 | in-del | -/A | 0.226864 | 0.249109 | intron-variant | BRWD3 | GRCh38.p7 | X:80691991 | AGCTAGGTATAAGAT[-/A]AAAAAAAAAAAAATT | 254065 |
rs765177261 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784324 | TAATTAGGAAAATTC[C/T]TAAAATTGTTACCAT | 254065 |
rs765182070 | snp | A/G | 2.29095e-05 | 0.00338441 | intron-variant | BRWD3 | GRCh38.p7 | X:80682097 | CTTCCCTTTTGGACT[A/G]GAAGTAAAAATATGT | 254065 |
rs765190131 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80755013 | ACTCCGTCTCAAATT[A/T]AAAAAAAAAGGAATA | 254065 |
rs765199697 | in-del | -/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670869 | TTTTTCCTAAATGCA[-/T]TTTTTTTTATTCTAA | 254065 |
rs765203810 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742715 | TCTGTTATTGGTGTA[C/T]AGGAATGCTTGATTT | 254065 |
rs765212516 | snp | C/T | 2.34066e-05 | 0.00342093 | missense, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704706 | TGCTTAGGTTTCTTC[C/T]GCCTTTCTTCTAGGG | 254065 |
rs765213192 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740617 | AGCCGGATGTGGTGG[C/T]GCATGCCGGTAGTAC | 254065 |
rs765217855 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725144 | AAGGTCTTCAGTGTG[C/T]TATCAGTTAGGTTCA | 254065 |
rs765220948 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746278 | GTTACAAACAACCTA[A/G]GTTTGTCTATGGGTT | 254065 |
rs765227841 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80684722 | CATAATTCATTTGAT[A/T]TTGATTAGGGAAGAG | 254065 |
rs765234462 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730848 | TCCCTAGCTTAACTG[-/T]TATTTCGTAGATCTA | 254065 |
rs765267710 | in-del | -/TTT | 0.00149365 | 0.0272873 | intron-variant | BRWD3 | GRCh38.p7 | X:80719061 | CTTGTCTTCAGTGTA[-/TTT]TTTTTTTTTATTCAA | 254065 |
rs765268982 | snp | G/T | 3.30158e-05 | 0.00406286 | intron-variant | BRWD3 | GRCh38.p7 | X:80709591 | TTCTGTAAAAGAGAA[G/T]AATAATAAATTTTAA | 254065 |
rs765272801 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753051 | CACTTGTTAATGGGA[C/T]TGTTTCTGAGTTTTG | 254065 |
rs765284089 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80801369 | GGGATTACAGGCGCC[C/T]GCCACCGCGCCTAAT | 254065 |
rs765324083 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722124 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGC | 254065 |
rs765333130 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754903 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCCAGAG | 254065 |
rs765341342 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80699201 | GCCTGGGCAACAGAG[C/T]GAGACTCCGTTGCAA | 254065 |
rs765351984 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80691246 | AACAAACATTTATTC[A/G]TATATAAACAAGAAG | 254065 |
rs765364376 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762947 | GTTAGGAATACCACG[C/T]AAAAGTTTGGTATTA | 254065 |
rs765381371 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80681101 | AGGTGTGAGCCACCA[C/T]GCCTGGCCCCATTTT | 254065 |
rs765381427 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697852 | AATGGAATTTGGGTA[C/G]TTCTACTTTAAGTCT | 254065 |
rs765392888 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672470 | AGGAAGGAGAAAAGA[A/G]AAAAGAAAGAAACCT | 254065 |
rs765445237 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674404 | GGTCAGCTCTTCATA[A/G]AAGAATGTCAACAAA | 254065 |
rs765449174 | snp | A/G | 0.000207967 | 0.0101951 | intron-variant | BRWD3 | GRCh38.p7 | X:80681969 | TTAAACCGAGATGCA[A/G]AACACCAAAAACAAA | 254065 |
rs765453067 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80743326 | AGGATTTTTGCATCG[A/G]TGTTCATCAAGGATA | 254065 |
rs765482498 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80800238 | GCATAATATCTCCTT[A/T]TTAAGAAGGGCTTCT | 254065 |
rs765485209 | snp | C/T | 5.23608e-05 | 0.00511641 | intron-variant | BRWD3 | GRCh38.p7 | X:80692069 | AAGAATTATAATTCA[C/T]TTTTTAAAAGCATAT | 254065 |
rs765495512 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790966 | GTAACATCCAAGCTA[C/T]GGAAAAGTATTTTTA | 254065 |
rs765500490 | snp | C/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723755 | ATGCTAACCTTTTCG[C/T]AGTATTTACTGCATC | 254065 |
rs765502879 | in-del | -/T | 9.35191e-05 | 0.00683746 | intron-variant | BRWD3 | GRCh38.p7 | X:80735942 | AATCAAGGCAATAGA[-/T]TAAAAAATTAACATG | 254065 |
rs765516725 | snp | A/G | 2.28517e-05 | 0.00338013 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716201 | TCTTTTCAACTGTAT[A/G]AAGACTGATTTCTAT | 254065 |
rs765520223 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80708770 | GCAGTGAGCCAAGTA[C/T]GTGTCACTGCACTCC | 254065 |
rs765539883 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765493 | TTTGGGTCACTTTAC[C/T]TTACTTTACTATTCT | 254065 |
rs765542455 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766961 | ACTAGGAGATTATAG[C/G]CCGCACCTGTCTCTG | 254065 |
rs765553550 | in-del | -/A | 0.0840797 | 0.187004 | intron-variant | BRWD3 | GRCh38.p7 | X:80711005 | TTGTTTCACCTCCTG[-/A]AAAAAAAAAAGAAAT | 254065 |
rs765560059 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809723 | AGAGTGAGTGAGTGA[C/G]AGAGAGAGAGAGAAG | 254065 |
rs765575249 | snp | G/T | 2.47445e-05 | 0.00351733 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691914 | TTCCTGGGGTTTGTA[G/T]AGCAAAGCAGTCAAT | 254065 |
rs765601278 | snp | C/T | 0.00018361 | 0.00957975 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686929 | TTCATAAATGAGGCT[C/T]AATAGTTCCTTGCAT | 254065 |
rs765604641 | snp | G/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670836 | TCAATCTCTGAATAT[G/T]GTAAAAAATCAGTCT | 254065 |
rs765612620 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80707630 | ATGTTCTTCTTAAAA[C/T]GCACATAATTATTGT | 254065 |
rs765640160 | in-del | -/A | 0.325363 | 0.23837 | intron-variant | BRWD3 | GRCh38.p7 | X:80735804 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 254065 |
rs765662830 | snp | C/G | 4.58695e-05 | 0.0047888 | intron-variant | BRWD3 | GRCh38.p7 | X:80733510 | TCCTAAGACATGAAA[C/G]AGATTTTTCGTTAAA | 254065 |
rs765671319 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734816 | TTTTTTTGTCAACTC[C/T]GGGCAGAATTTTTGT | 254065 |
rs765678963 | snp | A/C | 2.6833e-05 | 0.00366276 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80700025 | TCGATTTCCTTACAG[A/C]CCGAACATAAGCTTC | 254065 |
rs765679510 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780268 | TGGTGTATACTGAAA[G/T]AAAAATCTAAAGGAA | 254065 |
rs765699726 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781758 | AAGTAATCCCATTTA[C/G]TATAGCTATAAATAA | 254065 |
rs765724170 | in-del | -/TC | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671376 | AGAAGCATCCTAGTT[-/TC]TCAGATTAAAAAGTA | 254065 |
rs765724935 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781298 | CCTCCCCGTGTGCTC[G/T]CAGGCGATAGATGAG | 254065 |
rs765726246 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80698537 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAG | 254065 |
rs765737442 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80767603 | CCAAGATTTGGAAAA[A/T]CCAGAGCAGAAAAGC | 254065 |
rs765738299 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732878 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 254065 |
rs765798710 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80728159 | ATGCTTATGAATTGA[C/T]AGTTGAAACAGACAA | 254065 |
rs765845432 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748550 | GAAGACTTTTTATTA[A/C]CGACTCAATCTCATT | 254065 |
rs765850466 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80804485 | TCAAGTGATCCGCCT[C/G]CCTCAGTCTCTCAAA | 254065 |
rs765859171 | snp | G/T | 2.30274e-05 | 0.00339311 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80724943 | CTTACCATGTTAAAG[G/T]AATTCCGAATTTTGG | 254065 |
rs765867030 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780099 | AAACTTTTTAACTTA[A/G]TTTGGTTAATATACA | 254065 |
rs765879408 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739454 | AATGGAGATGGAAGT[C/T]TGAGAATCATCAGTT | 254065 |
rs765884439 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721126 | TAATGAGTACAAAAT[G/T]TTTATATACACTGAA | 254065 |
rs765886122 | in-del | -/TCT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766929 | GTGCTTTCCCAACGG[-/TCT]TCTTAGCAAATGGCA | 254065 |
rs765907564 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80720882 | ATACAAATATGTACC[A/T]TTGTATGTATAACTG | 254065 |
rs765935240 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80686622 | TCTGAAATAAAAGTC[A/G]GAAAGAACAGCAAAT | 254065 |
rs765939864 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80758195 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAATAA | 254065 |
rs765942717 | snp | C/T | 4.57446e-05 | 0.00478228 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734213 | CAGTTGTAATGAACA[C/T]ACCACCTAGAAGATT | 254065 |
rs765947246 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80708668 | TAAAAATACAAAAAT[G/T]AGCCATGCATGGTGG | 254065 |
rs765954777 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80781207 | GAGTGAAAACAGAGC[A/T]CCCATAAAATGGGAG | 254065 |
rs765959096 | snp | C/G | 4.13924e-05 | 0.00454912 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809487 | CCTTTTCCCGAGGGG[C/G]TTTGGGGGCTTCGCT | 254065 |
rs765959733 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726306 | TAACACGTTTACATG[A/T]TATGTCTGTATAACA | 254065 |
rs765963543 | snp | G/T | 3.30404e-05 | 0.00406437 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703584 | CTGCTATAGAAACCA[G/T]TCCTCCTTTCTAAAA | 254065 |
rs765995644 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721808 | TTGCATTTCAAACAC[A/G]AGGATAGGTAAATAG | 254065 |
rs766002701 | snp | A/C | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80727260 | CATTCCAATCTATTC[A/C]CTCTTCTGTGACCAG | 254065 |
rs766050349 | snp | A/G | 2.28605e-05 | 0.00338079 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80693040 | CATCTATTATACTGC[A/G]GAATCTATCACCTAT | 254065 |
rs766068647 | snp | C/T | 0.0282 | 0.115346 | intron-variant | BRWD3 | GRCh38.p7 | X:80712605 | GCGTCTCTGCCTGGC[C/T]GCCCATCGTCTGGGA | 254065 |
rs766094364 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732462 | CAAGACAACTAAAAG[C/T]TGGAACATTCAGGAA | 254065 |
rs766113741 | snp | A/G | 2.29003e-05 | 0.00338373 | intron-variant | BRWD3 | GRCh38.p7 | X:80744267 | CCCTATAGTAACAAA[A/G]GGACAATAGGTTTAT | 254065 |
rs766118800 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80713146 | CCGCCCCTACTGGGA[A/C]GTGAGGAGCCCCTCT | 254065 |
rs766140302 | in-del | -/TT | 0.000338827 | 0.0130115 | intron-variant | BRWD3 | GRCh38.p7 | X:80682124 | ATGTAACAACGAGCA[-/TT]TTTTTTTTTCTGTTA | 254065 |
rs766147679 | snp | C/T | 2.3067e-05 | 0.00339602 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691856 | TGATGCCCTGAATAA[C/T]CCGTTCACATTCTTC | 254065 |
rs766163630 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754964 | AGTAAGCCGAGATGG[C/T]GCCACTGGACTCCAG | 254065 |
rs766165315 | snp | C/T | 2.3232e-05 | 0.00340815 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686981 | TTACACTTTAAAGAC[C/T]GTCTTCTGCCTCGGC | 254065 |
rs766169298 | snp | C/G | 2.86952e-05 | 0.00378772 | intron-variant | BRWD3 | GRCh38.p7 | X:80692047 | GTGATTACCATTTTA[C/G]TTTTAAAAGAATTAT | 254065 |
rs766189645 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703095 | AGTAAATACCTTCTT[A/G]TATACTTTCTATCAG | 254065 |
rs766196761 | in-del | -/A | 0.004083 | 0.0449981 | intron-variant | BRWD3 | GRCh38.p7 | X:80691992 | AGCTAGGTATAAGAT[-/A]AAAAAAAAAAAATTA | 254065 |
rs766196859 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748460 | AGAGTTTGAAAAACA[A/T]TAGTGTAAGTTCTGC | 254065 |
rs766201503 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740939 | TTATACTTTAAGTTT[G/T]AGAGTACATGTGCAC | 254065 |
rs766205093 | snp | A/G | 2.287e-05 | 0.00338149 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676800 | GCAGTCTACTGAAAC[A/G]TCCTGAAAACATGGT | 254065 |
rs766205109 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80687339 | CGGTAGTTAAGTATA[C/T]TTGACAATGGCATCA | 254065 |
rs766243885 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678849 | TCATATGTGGAAGCC[C/T]TAATCCCCGAAGTGA | 254065 |
rs766276932 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810394 | TTTACCAAATGAAAA[C/T]GTTGTACTTACCAGT | 254065 |
rs766277934 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694514 | GCTGCGGACACTCAA[C/T]GCCAGCCTGTGAAAG | 254065 |
rs766281429 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744490 | TTTTCAAAATTACCA[-/C]CAATACTGACAATGC | 254065 |
rs766293361 | snp | A/G | 2.28566e-05 | 0.0033805 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682066 | CATTTTTAGGCTGCA[A/G]CTTCATTTGTTTCTG | 254065 |
rs766295452 | in-del | -/GTAACT | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80683292 | TCCTGGAAGTAAACA[-/GTAACT]GTAAGTAAAAATAGG | 254065 |
rs766306533 | snp | C/T | 2.97265e-05 | 0.00385518 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745696 | TGACCAAAGCGACTA[C/T]AGCCGGTTAATTGCC | 254065 |
rs766336734 | snp | A/G | 2.32415e-05 | 0.00340884 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723754 | TATGCTAACCTTTTC[A/G]TAGTATTTACTGCAT | 254065 |
rs766337399 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674845 | TAACCCTACTGCCGA[C/T]CCTACCAAAAAAGCA | 254065 |
rs766363097 | in-del | -/CA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754150 | TTTACAGTCCATGAG[-/CA]CAGGCTATTTTTCTA | 254065 |
rs766365860 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80693634 | TGCTATAATAAAGAC[A/C]CTGGCAGCATTTTGC | 254065 |
rs766366660 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727440 | TTCTGCTCTCTGTGA[C/T]ATAGCTAAATTGGCT | 254065 |
rs766367732 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759248 | TGCACAAACACCTGT[A/T]GAATAAACCTGTCTA | 254065 |
rs766378366 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80738589 | CAAAAAAATGAAACA[A/G]AAGGGAAGATACAGA | 254065 |
rs766386241 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795366 | TACACACACACACAC[-/AT]ATGTGTATATATACA | 254065 |
rs766408963 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80760826 | TCTGCTAAAATATTA[G/T]TATTAGAAAAAAAGT | 254065 |
rs766410033 | snp | A/G | 0.0026455 | 0.0362733 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810269 | GCGGTTTTGTTTGCT[A/G]TTTATACTCTACCCC | 254065 |
rs766454817 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80716670 | CTTTTCTGTAGCTGA[A/C]TGATATGCCATTTTG | 254065 |
rs766462804 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80725995 | TATGTCTATATAACA[C/T]AACATGTTTACATGT | 254065 |
rs766471460 | in-del | -/A | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810927 | TATTTACATTGAAAT[-/A]ATTACAATTTGAAGG | 254065 |
rs766473559 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740374 | ATTTTAAGTTATCCA[C/T]GACTTTCACTACCAA | 254065 |
rs766479437 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721950 | CTCCTGGGTTCAAGC[A/G]GTTCTTGTGCCTCAT | 254065 |
rs766484637 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80769732 | AGCAGAAGGCAAGAA[A/C]TAACTAAGATCAGAG | 254065 |
rs766487938 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729334 | GTAATTAAATATGAC[A/G]TTATCAATGGGCGAC | 254065 |
rs766493538 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786015 | GCCTGTGCAACAGTG[C/T]AAGACTCTGTCTCAA | 254065 |
rs766501282 | snp | C/G | 5.8944e-05 | 0.00542849 | intron-variant | BRWD3 | GRCh38.p7 | X:80685426 | TTTAGAAAGTAAAAA[C/G]AATCAATATGTCTTT | 254065 |
rs766502194 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769515 | AATAATGAAATGAAG[A/G]CAGAAAAAAAGATGA | 254065 |
rs766502418 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711928 | TTAGGCATATGTTCT[A/C]GGGACTACTTCTTGA | 254065 |
rs766502616 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700826 | TATAGCATTTACATT[A/G]TATTAGGTATCATAA | 254065 |
rs766564032 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695104 | TGAGTTTTCACAAGA[A/T]CTGATGGTTTAAAGG | 254065 |
rs766571220 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80690171 | ACAATATGGAACAAA[C/T]ATGTACTTAAACACA | 254065 |
rs766590431 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711184 | AAGTGCTAAGATATA[C/T]AAGTGGATTTAATAA | 254065 |
rs766609628 | in-del | -/A | 0.000530504 | 0.0162779 | intron-variant | BRWD3 | GRCh38.p7 | X:80762069 | AAAAATGCAAGAGAC[-/A]AAAAAAATACAGCTG | 254065 |
rs766612941 | snp | A/G | 0.000100183 | 0.00707682 | intron-variant | BRWD3 | GRCh38.p7 | X:80729893 | TCATGAGAACCACAT[A/G]AACATCTAACATATA | 254065 |
rs766632178 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743187 | GGTTCTGTTTATATG[C/T]GGGATTATGTTTATT | 254065 |
rs766658667 | snp | A/G | 0.00468538 | 0.048174 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809700 | AGAGGAGAGGGAGAG[A/G]GAGAGAGAGAGTGAG | 254065 |
rs766662066 | in-del | -/T | 8.54482e-05 | 0.00653581 | intron-variant | BRWD3 | GRCh38.p7 | X:80730071 | AAAAATGTAAATCAC[-/T]TTTTTTTGATAATAT | 254065 |
rs766698239 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768186 | GGAGAACTTCCCCAA[-/C]CTAGCAAGGCAGGAG | 254065 |
rs766701550 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732505 | GGGCATGAACCGTAA[A/G]AGGAAGATAAGACCT | 254065 |
rs766706068 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773587 | AAGCTAACTAAGCTA[A/G]CTCAGTCCCTTGGAT | 254065 |
rs766708938 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784132 | GGTGATGGGCACCTC[A/G]TTTACCTTCAGGTGA | 254065 |
rs766714947 | in-del | -/AT | 3.14154e-05 | 0.00396317 | intron-variant | BRWD3 | GRCh38.p7 | X:80696037 | TATAGAGATATAACA[-/AT]ATATGTTACTAAATG | 254065 |
rs766723499 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783269 | GTGCACACCTGTAGT[A/C]CCAGCTACTAGGAGG | 254065 |
rs766726202 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771153 | ATACGAAGAATCAGT[A/T]TCGTGAAAATGGCCC | 254065 |
rs766741131 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80680863 | ACACGGGCTGGAGTG[C/T]AGTGGCACAATCACA | 254065 |
rs766750511 | snp | A/T | 0.0152462 | 0.0859689 | intron-variant | BRWD3 | GRCh38.p7 | X:80714190 | GCTTCATCTGCATAA[A/T]AAGAATCTTGGTCTT | 254065 |
rs766752662 | snp | A/C/G | 2.31353e-05 | 0.00340105 | intron-variant | BRWD3 | GRCh38.p7 | X:80724886 | CAAGTTATTATATGA[A/C/G]AGAAGTTGGTTTTAA | 254065 |
rs766759027 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726420 | TTATATGTTTATATG[C/T]CTCATAAAGGAAAAG | 254065 |
rs766761302 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80697607 | CAGCTGTTTTACTTA[C/T]GATAATGGCCTCCAG | 254065 |
rs766787821 | snp | C/T | 5.4936e-05 | 0.0052407 | intron-variant | BRWD3 | GRCh38.p7 | X:80808964 | CTTGCCCTCCCCTTC[C/T]TCCAGTCTCACCTCA | 254065 |
rs766801649 | snp | A/G | 3.06288e-05 | 0.00391324 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80699977 | GATCCATTTTGTTCC[A/G]TGGCTGTTTTTGTAA | 254065 |
rs766803495 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80752970 | ACGCCTGGCCGATCA[C/T]TTTTTTGTATACCTG | 254065 |
rs766813864 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757628 | TATTCAGAATCCATT[C/G]TCTCTTAGATATTTG | 254065 |
rs766815835 | snp | A/G | 2.31262e-05 | 0.00340038 | synonymous-codon, intron-variant | BRWD3 | GRCh38.p7 | X:80684028 | TGACTTTTTATTAGA[A/G]GTATAAGCTTTGGAG | 254065 |
rs766816780 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80766373 | CAGCCTCCATAATCA[C/T]ATAAACGACTTCCTT | 254065 |
rs766832492 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735041 | CAATTAACACTCAAA[C/T]GTGTATCTTTTTTCT | 254065 |
rs766841711 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801508 | GGCGTGAGCAACCGC[A/G]CCCGGACGAGAAAAC | 254065 |
rs766850333 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754742 | CCGGGCATGGTGGCT[C/T]ACGCCTATTATCCCA | 254065 |
rs766851945 | snp | A/G/T | 5.25766e-05 | 0.00512699 | intron-variant | BRWD3 | GRCh38.p7 | X:80707525 | CAAAGAGCCAGCAAT[A/G/T]AAGATATATGGATAT | 254065 |
rs766854351 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788490 | GACAGTATCAGAAGA[G/T]GGTGAGAATGTGGGA | 254065 |
rs766860279 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80681600 | GTTATTTTATTCTAA[C/T]ACCAAAATTATAAGT | 254065 |
rs766876133 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789438 | TGGAGTGCAGTGGCG[C/T]GATCTCGGTTCACTG | 254065 |
rs766879646 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779665 | AACTAAACAGATTAA[C/T]ATAGACTAAAATCTT | 254065 |
rs766905886 | snp | G/T | 4.66271e-05 | 0.00482819 | intron-variant | BRWD3 | GRCh38.p7 | X:80696694 | AATATACAATAGGTA[G/T]TAAAATACACACACT | 254065 |
rs766925636 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688801 | AATTTCAAACTAAAA[C/T]ATATTTATGTGAAAG | 254065 |
rs766928323 | in-del | -/ATA | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80799021 | GGCAGCTGAAAAATT[-/ATA]ATGATAGCAATCATT | 254065 |
rs766930503 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729667 | GAATGGCTCTGTAGG[C/T]ATCAGTAGAACACAG | 254065 |
rs766934390 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669685 | ACTTAACAGACTATA[C/T]AAAATTGCCAATACA | 254065 |
rs766957322 | snp | G/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80735676 | AGGCATAGTGGCGGG[G/T]GCCTGTAGTCCCAGC | 254065 |
rs766984838 | snp | C/G | 2.82167e-05 | 0.003756 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745672 | TGGTAAGCAGATGAA[C/G]GGAAAATATGACCAA | 254065 |
rs767003113 | in-del | -/A | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80788382 | TCAAAACTCAATAAT[-/A]AAAAAAACGCAAACA | 254065 |
rs767024917 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672136 | AATGGGCATACATGT[A/G]AATAAACAAACACAA | 254065 |
rs767037435 | snp | G/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80726379 | TTTACATGTTATATC[G/T]GTATAACATAACATG | 254065 |
rs767052508 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80686507 | CTAAGTGGCCATATT[A/G]ATAACACATTCAGTA | 254065 |
rs767057120 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756489 | CCTGGGCAACAAGAG[C/T]GAAACTCTGTCTCAA | 254065 |
rs767077958 | in-del | -/AC | 0.42221 | 0.181229 | intron-variant | BRWD3 | GRCh38.p7 | X:80696519 | ATCCATAACATAAAT[-/AC]ACACACACACACACA | 254065 |
rs767078012 | snp | C/T | 9.73568e-05 | 0.00697631 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707471 | AACAGGATCCTCTAC[C/T]GAAGCGTCACTTGTG | 254065 |
rs767088849 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669484 | TAAACGTACGGAAAT[A/C]ATTCAGAACTACCAG | 254065 |
rs767112713 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766696 | TCCCAGCGTGATCGA[C/T]GCAGAAGATGGGTGA | 254065 |
rs767128799 | snp | A/G | 3.37348e-05 | 0.00410685 | intron-variant | BRWD3 | GRCh38.p7 | X:80809316 | AGCTCTGGGGAAGAG[A/G]GGGGAAAAGAGGTTC | 254065 |
rs767165195 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714639 | CCCGACCATCTCAGG[C/T]ACAGAGTCTCAGGAT | 254065 |
rs767175895 | snp | C/T | 2.27959e-05 | 0.00337601 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722630 | CGTCCTGGTACCAAC[C/T]GTTGGAATTTTGTGG | 254065 |
rs767189184 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80676510 | ACCAATGTGAAAGGA[A/G]GCAGAAGTCCCCACA | 254065 |
rs767213050 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703544 | AAGATCCACTGAGGG[A/G]CAAACCATTCTTCAT | 254065 |
rs767219277 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781583 | CTGAACTGGGGCATA[A/G]TAGGGGTCGTGCAGT | 254065 |
rs767227817 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746422 | GCTTTGCCTTGTTCT[G/T]CATTTTCTTAAAAAA | 254065 |
rs767236370 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775253 | AAAAATTTGCAGACT[C/T]CTGGCATAGAGGATG | 254065 |
rs767261433 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804947 | CTGGAAAATTTAGAG[C/T]GTTATATTTTAAATG | 254065 |
rs767266353 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685854 | GTAAGCTCATAGGAC[A/G]GTCTGATGTATTTCT | 254065 |
rs767274392 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779598 | TACATGCCTGTAGTC[C/T]CAGCTAGTTTTTGGT | 254065 |
rs767281588 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80739354 | TTCAATAATGAATAT[A/G]ATGAGTTTGAAATAC | 254065 |
rs767282246 | in-del | -/TAAAA | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80778836 | ACACCCTGTCTCTAC[-/TAAAA]ACACAAAAATTAGCT | 254065 |
rs767296038 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80703062 | TTGCAAAACTACATT[C/T]CCCTGCTCATTTAAA | 254065 |
rs767318050 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724706 | TTGAGTATCTGTAGT[A/T]TGGGACTGGGGAACA | 254065 |
rs767318697 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80720879 | GATATACAAATATGT[A/T]CCATTGTATGTATAA | 254065 |
rs767319846 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740254 | ATCTCCTCCAAAAGT[A/G]GTCTCTTTCTCCAAA | 254065 |
rs767325042 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80712060 | CTTAAGAGGTAAAAA[A/G]TATCTTTAGAATAAA | 254065 |
rs767351180 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678002 | TATAACCAGAGTGGA[A/T]TAGAAAAACAGTGAG | 254065 |
rs767386364 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80793977 | TGAGGTCAGAAATTC[A/G]AGACCAGCGTGGCCA | 254065 |
rs767387656 | snp | A/C | 2.30798e-05 | 0.00339696 | intron-variant | BRWD3 | GRCh38.p7 | X:80691047 | AGTGATTAAAAAAAA[A/C]CAGACCTGTAAAAGC | 254065 |
rs767394801 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730982 | TTTCCAATCTTCACC[A/G]TTATAAATAATGCTG | 254065 |
rs767418009 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753128 | AGATGGATAATTTGC[A/G]ATTATTTTCTCCAAT | 254065 |
rs767426445 | in-del | -/ACC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709922 | CAGACCTGTGCTGGA[-/ACC]ACATTTAGAAACCAG | 254065 |
rs767443934 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706439 | CCTTACTCTATAAGG[-/T]TTTTTTCTATTTTTA | 254065 |
rs767455809 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80794530 | AAATAAATAAAAAAA[-/T]ATATATATATCTCTA | 254065 |
rs767458650 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80692547 | GCCTAGAATTCATAC[A/G]ACTAAACAAAAGACT | 254065 |
rs767477409 | in-del | -/G | 1.74287e-05 | 0.00295196 | intron-variant | BRWD3 | GRCh38.p7 | X:80692000 | TAAGATAAAAAAAAA[-/G]AAAATTAGAAAAAAT | 254065 |
rs767480047 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796168 | CGGAGTCTCGCTCTG[C/T]CACCCAGACTATAAT | 254065 |
rs767501567 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80784501 | ACCTAGGTATTGAGT[C/T]CCACATGCATTAGCT | 254065 |
rs767505482 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726129 | TATAACATATAACAC[A/G]TTTACATATGTCTGT | 254065 |
rs767514271 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811309 | TATTCTTTATCCAAA[C/G]TGCTTGGGACCAGAA | 254065 |
rs767524006 | snp | A/G | 2.33517e-05 | 0.00341691 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709542 | TTTGCGCTGTGTCCT[A/G]CGTAAAGAACGCCCA | 254065 |
rs767526100 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762998 | AGTGATCGCTACTAT[A/G]AAGAAAATAAAATAA | 254065 |
rs767546818 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702984 | AATTTTGATTAATTT[C/T]TGACTGGCCAATAAT | 254065 |
rs767547135 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768485 | CAGCCAAACTAAGCT[G/T]CATAAGTGAAGGAGA | 254065 |
rs767555361 | snp | C/T | 2.28391e-05 | 0.00337921 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682553 | TCTGACTCTGGATTG[C/T]TGACTTATATTCAGA | 254065 |
rs767558942 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773286 | ATTTCCTGAGTCTTA[A/G]GCCAAACATCTCCCG | 254065 |
rs767564114 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737695 | AAAAAATTAGCTGGG[C/T]ATGGTGGCACATGCC | 254065 |
rs767603827 | snp | A/G | 4.68137e-05 | 0.00483784 | intron-variant | BRWD3 | GRCh38.p7 | X:80683972 | CAGTAACTGGTTAAA[A/G]AAAACTGCCTGATAA | 254065 |
rs767611442 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789110 | CCATGGCTAATACTC[-/T]TATCTTTGGAGCTCT | 254065 |
rs767622953 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806851 | ATGTCTTTACAATAT[A/G]AGGAAAAGTCTAGTA | 254065 |
rs767636083 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719056 | TGCTTCTTGTCTTCA[A/G]TGTATTTTTTTTTTT | 254065 |
rs767636217 | in-del | -/AA | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80801129 | ATATATCATGCTTCT[-/AA]AAAAAGTTAAGAAAA | 254065 |
rs767661061 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785904 | GCATGGTGGCAGGAG[C/G]CTGTAATCCCAGTTA | 254065 |
rs767667525 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759740 | ATACAAAAGCAGTGA[C/T]TTCATATGGCTCAAC | 254065 |
rs767674960 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739997 | GACAGTATGTCCCAA[C/T]TCCAGAAATAATCAG | 254065 |
rs767676662 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80717041 | CCTTTCTCTTTTCTA[A/C]ATCTATTTCCAGTTG | 254065 |
rs767676792 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671691 | AATCAAGCCAGTTTA[C/T]ATTACCTTTTTTACT | 254065 |
rs767696195 | snp | C/T | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673162 | AGTTAAATATCTGAG[C/T]GCACAGTTGTGCAGA | 254065 |
rs767722492 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80760576 | CACTGGAATATTATT[C/T]ACATATTTAAATTGC | 254065 |
rs767744853 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80700649 | GGCTGACGCAGGAGA[A/G]TCACTTGAACCCGGG | 254065 |
rs767758107 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679414 | CAAGTTTGAGATGCG[A/T]AGATAAGCAACCGAA | 254065 |
rs767762373 | in-del | -/CACG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750891 | ACACACACACACACA[-/CACG]CAAAAATCATTAAGT | 254065 |
rs767763612 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670166 | TTGGGGGAAAAATCG[A/G]TACCGTAAAAAGTTT | 254065 |
rs767771943 | snp | C/T | 2.34291e-05 | 0.00342257 | intron-variant | BRWD3 | GRCh38.p7 | X:80723743 | CAAAATTTAAATATG[C/T]TAACCTTTTCGTAGT | 254065 |
rs767812307 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769095 | AGATTCATAAAGCAA[A/G]TCCTTAGAGACCTAC | 254065 |
rs767815983 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792011 | TTTTTTAACCATGTC[C/T]CAGAAGCAAATGTCT | 254065 |
rs767817651 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689655 | GCTGGTATTCAGCCA[A/G]ATTTCAAAAATCTGT | 254065 |
rs767835399 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80760997 | AGTTGCAGTGAACTA[A/T]GATCTTGTCAGTGAA | 254065 |
rs767838757 | snp | C/T | 5.16556e-05 | 0.00508184 | intron-variant | BRWD3 | GRCh38.p7 | X:80729876 | ACTCAATGTAAAATA[C/T]ATCATGAGAACCACA | 254065 |
rs767846029 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789529 | TACAGGCGCGTGCCA[-/C]CACGCCCAGCTAATT | 254065 |
rs767855271 | snp | A/C/G | 4.66393e-05 | 0.00482886 | intron-variant | BRWD3 | GRCh38.p7 | X:80808633 | AAAGGGGGAAGCGGA[A/C/G]GCAAATGATGAAGGA | 254065 |
rs767857242 | snp | G/T | 2.5493e-05 | 0.00357013 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728779 | AAGAAGCTGTCCTGT[G/T]ATAGAATTCCACACT | 254065 |
rs767861701 | in-del | -/AAAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80720556 | GAAAAGTTAAAAAAC[-/AAAC]AAACAAACAAACAAA | 254065 |
rs767908479 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791109 | CTGAGGCTAAACTAC[-/A]TAAGCTTAATGTATA | 254065 |
rs767910371 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80738150 | AAACCTTTATCTCCA[A/T]TGCATTTAAATTGCT | 254065 |
rs767915254 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80713662 | GCCAAATCCCCCTCT[C/G]CGAGAGACACCCAAG | 254065 |
rs767941770 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80723213 | CAAAGGCACTCAAAC[C/T]TGATATTAATGCAAT | 254065 |
rs767946824 | snp | C/T | 4.87199e-05 | 0.00493534 | intron-variant | BRWD3 | GRCh38.p7 | X:80719459 | TTACAGTACATAAAC[C/T]ACACCCTTTACAAGT | 254065 |
rs767958916 | in-del | -/AATATGAAA | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80680720 | CTCTCCTTTCTTATT[-/AATATGAAA]AATATGAAAAATCCT | 254065 |
rs767961642 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80752038 | TATTATTTTAAACAC[A/G]ATCTTGCTTTGTCGC | 254065 |
rs767961687 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80741540 | AACAGTGTAAAAGTG[G/T]TCCTATTTCTCCATA | 254065 |
rs767966163 | snp | C/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671581 | TTTTATTGTAAACAT[C/G]CCATAAAGAATGGCA | 254065 |
rs767968836 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80797177 | TCTGGAAAAAAAGTC[C/T]TAAGGTGCTGCATAT | 254065 |
rs767972255 | snp | C/T | 2.41086e-05 | 0.00347185 | intron-variant | BRWD3 | GRCh38.p7 | X:80735231 | TGTTTTTGTGTTTCA[C/T]CATGTTTGGCTAATG | 254065 |
rs768036437 | snp | G/T | 2.28035e-05 | 0.00337657 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717639 | ATGAGATCTCTTTCA[G/T]TGGCCATCTGGCTCC | 254065 |
rs768063593 | snp | G/T | 9.15227e-05 | 0.00676409 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676840 | ATCATCTGCAATACG[G/T]GCTCGTTTGGCTCTG | 254065 |
rs768071366 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751075 | AACAGAGTAGAAAGG[C/T]AGTTACCACAGGATA | 254065 |
rs768076815 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730467 | ACAGTTAACACAGAT[C/G]AATCTTGAATAGGCA | 254065 |
rs768114085 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80690771 | CTTAATAACGATGAA[A/T]CCACAAACCACTTAA | 254065 |
rs768122271 | snp | C/T | 5.23931e-05 | 0.00511799 | intron-variant | BRWD3 | GRCh38.p7 | X:80691223 | AAAGGACATTAACAT[C/T]TCATGGTAACAAACA | 254065 |
rs768130257 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669423 | ATAGGGTCAGACTAG[A/G]CAAAAACACTTGTTT | 254065 |
rs768131702 | in-del | -/GTATGAACTTTAAA | 0.493957 | 0.0546337 | intron-variant | BRWD3 | GRCh38.p7 | X:80742409 | CTCTTTTTTGGTTCT[-/GTATGAACTTTAAA]GTAGTTTTTTCCAAT | 254065 |
rs768146163 | snp | C/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675336 | TGATTCATAATACTA[C/G]CTAGCCAAAACATTC | 254065 |
rs768204420 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80783930 | AGGCTGGGAAGGATA[A/G]TGGGAAAGAGCGGGG | 254065 |
rs768209298 | snp | A/G | 2.28316e-05 | 0.00337865 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734119 | TGATTTTCTCTTACC[A/G]TATGTGACTCTAATT | 254065 |
rs768212341 | snp | A/G | 2.31217e-05 | 0.00340004 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709526 | GGTAAGTATGCTGAC[A/G]TTTGCGCTGTGTCCT | 254065 |
rs768215926 | snp | G/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673670 | ACACACACTAAGATC[G/T]TAAAGCTGGGAATTT | 254065 |
rs768251025 | snp | A/T | 4.57844e-05 | 0.00478436 | intron-variant | BRWD3 | GRCh38.p7 | X:80692004 | GATAAAAAAAAAAAA[A/T]TTAGAAAAAATTATT | 254065 |
rs768254571 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680662 | TATTTTTACTGCAGT[A/G]GGCCACAAAAATATG | 254065 |
rs768300763 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805516 | TGTAATGCTGCTATA[C/T]AATGTAATATTCCAG | 254065 |
rs768301113 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766817 | TGGGGCACTGCCTCA[C/T]GCCGGAAGTGCAAGG | 254065 |
rs768305736 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748016 | TGGCGAGAATGGGCA[A/T]CTTTTTATTAGAGAT | 254065 |
rs768308564 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756597 | GTACTGATTCTTGCT[C/T]TACTTACTACAGTAG | 254065 |
rs768309390 | snp | C/G | 4.57629e-05 | 0.00478324 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681449 | AAGAAAATGGCCCAT[C/G]TGGCTCATCATCAAG | 254065 |
rs768313792 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743003 | ATGCTTCCAGTTTTT[G/T]TCCATTCAGTGTGAT | 254065 |
rs768330950 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773251 | AGTAAAACTGAGGAC[A/G]TCTGATATGACCACA | 254065 |
rs768345817 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80751878 | CCTCCAGTTCCATCC[A/G]TATTGCTGCAAATAA | 254065 |
rs768372693 | snp | A/C | 0.00498063 | 0.0496602 | intron-variant | BRWD3 | GRCh38.p7 | X:80809420 | CTTAGCACCCCCCCA[A/C]CCCCCGACACAGCTA | 254065 |
rs768388916 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715680 | ATACAATCTCTGTTA[C/T]AACTATTCAATTCTG | 254065 |
rs768419329 | in-del | -/AA | 0.000666889 | 0.0182483 | intron-variant | BRWD3 | GRCh38.p7 | X:80798625 | GTGTATAATACGGGG[-/AA]AAAAAAAAAAAAGAG | 254065 |
rs768420398 | snp | G/T | 3.21043e-05 | 0.00400638 | intron-variant | BRWD3 | GRCh38.p7 | X:80730050 | AATAACTTTATTAAT[G/T]TTCTCAAAAATGTAA | 254065 |
rs768422628 | in-del | -/TA | 1.66128e-05 | 0.00288204 | intron-variant | BRWD3 | GRCh38.p7 | X:80745534 | CAATTGTTGTAATTC[-/TA]TATATGTTACCATAT | 254065 |
rs768423759 | in-del | -/ATAAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725856 | GTGTTACATGCCTAT[-/ATAAC]ATAACATGTTTACAT | 254065 |
rs768437753 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797967 | GGGTCTGGTTGTAAG[C/T]GCCTGTAGTCCCAGC | 254065 |
rs768447919 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701320 | TGGGAGGCCGAGATT[C/G]GTGGATCACCTGAGG | 254065 |
rs768463328 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687176 | AGTATTTTCCCTGGC[A/G]AAAATAATTAGTGAG | 254065 |
rs768464825 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767348 | CTGGGACAAAGCTTC[C/T]AGAAGAAGTATCAGG | 254065 |
rs768476847 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714898 | TTGGCAGTATGTTCA[C/T]TTAGTAAACAGGTCA | 254065 |
rs768479161 | snp | G/T | 2.49529e-05 | 0.00353211 | intron-variant | BRWD3 | GRCh38.p7 | X:80684173 | TAATCCTACAAAGAA[G/T]AATGTGTTATTAAAT | 254065 |
rs768506871 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735437 | TACTTACTACTACCA[G/T]TATGAGAAATCTTCT | 254065 |
rs768507350 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779375 | GTTAAAGTGTAGTAA[C/G]CATATTAGTTTCTAT | 254065 |
rs768510317 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715515 | CCTGAGAGTATTCTG[C/T]TTAGCAGTTTCTTTC | 254065 |
rs768518285 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806890 | TGTTGGGGTTTTTTT[-/G]GTGAGGAGACTATTT | 254065 |
rs768532851 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766398 | TTCCTTATAATAAAT[A/G]CATCTATCAATCCTA | 254065 |
rs768544775 | snp | A/C/G/T | 0.000232907 | 0.0107894 | intron-variant | BRWD3 | GRCh38.p7 | X:80808632 | GAAAGGGGGAAGCGG[A/C/G/T]GGCAAATGATGAAGG | 254065 |
rs768554021 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804739 | AATTAGCCAACAACT[A/C]AATAGGGTCACCACA | 254065 |
rs768563039 | snp | C/T | 4.79743e-05 | 0.00489743 | intron-variant | BRWD3 | GRCh38.p7 | X:80699910 | GGGTAAGCAATTTAA[C/T]TCCAAAGCTACTTCC | 254065 |
rs768566865 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80757230 | AGGCTCTATTTACTA[A/C]AAAATTTAACTCCAC | 254065 |
rs768593344 | in-del | -/AGC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721494 | AAGCCTTAATTCCCT[-/AGC]AGCAATGATATGAAA | 254065 |
rs768598242 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80765421 | ACAAGGCTGGTGATT[A/T]ACAACAATACAATCC | 254065 |
rs768606181 | snp | C/T | 4.71971e-05 | 0.0048576 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677284 | TTCATCTTCTTCTGA[C/T]GCACTAAGTAGTTTT | 254065 |
rs768623056 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80789350 | GATCTTAATAGATAT[A/T]CTGGAAAGAGTTTCC | 254065 |
rs768625821 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727741 | TGAGATTGGGTAATT[C/T]CTACTTATCTTTCAA | 254065 |
rs768633763 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720860 | TTCTGTCTAGATATG[A/C]TTAGATATACAAATA | 254065 |
rs768645773 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782636 | GGCACAGTGACTCAC[G/T]CCTGTAATTCCAATA | 254065 |
rs768661437 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80679181 | CTTGTTATGGAAACC[C/T]AAGCTGACTAATACT | 254065 |
rs768663927 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748261 | TTGGTGATCTGCCCA[C/T]CTCGGCCTCCCAAAG | 254065 |
rs768671244 | snp | A/T | 1.64757e-05 | 0.00287012 | intron-variant | BRWD3 | GRCh38.p7 | X:80728956 | AATTTTTGACAAAGG[A/T]GCATGTTAAATAGCA | 254065 |
rs768709733 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705720 | TCAACAATTTTAACA[C/G]AATGCTAAGTATATA | 254065 |
rs768709810 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728252 | CATCAACACTACCCA[C/T]GTGATTTCTGCTATT | 254065 |
rs768745819 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80789549 | CCCAGCTAATTTTTC[A/G]TATTTTTTAGTAGAG | 254065 |
rs768749515 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777152 | CTTAAGACCCCCCCC[A/C]ACGAAAAACCTCCTG | 254065 |
rs768749794 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688260 | GCAAGTAGAACAAAA[G/T]ATAGAGGGAGACTCA | 254065 |
rs768761156 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754823 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 254065 |
rs768768471 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784570 | AGGCCCTGGTGTGTG[C/T]TGTTCCCCCGCCCTG | 254065 |
rs768768723 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707296 | TCACATCAGGTCTCT[C/T]GGCTTCCAGCCAATA | 254065 |
rs768792272 | snp | A/T | 2.47161e-05 | 0.00351531 | intron-variant | BRWD3 | GRCh38.p7 | X:80719444 | GTAAAAGTAAAATAA[A/T]TACAGTACATAAACT | 254065 |
rs768796177 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741178 | GGTTTTTTGTCCTTG[A/C]GATAGTTTGCAGAGA | 254065 |
rs768808393 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679527 | TTTGGAGAGTCATCA[C/T]ATCAAGATGACGGAT | 254065 |
rs768821221 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798020 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC | 254065 |
rs768828903 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80786172 | GCCACATGTGGTTGC[A/T]GAATGTCAAATTACT | 254065 |
rs768841635 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711048 | AGAATTTGCCCATTC[A/G]TAATTTACGTATGCC | 254065 |
rs768848893 | in-del | -/T | 0.221969 | 0.248424 | intron-variant | BRWD3 | GRCh38.p7 | X:80764472 | ACCACGCCTGGATAA[-/T]TTTTTTTTTTTTTTG | 254065 |
rs768856092 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80733864 | TTGAAAATAAATCAA[C/T]CATTTCCTGTTTCCC | 254065 |
rs768856243 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80725980 | CATGTTTACATGTTA[C/T]ATGTCTATATAACAT | 254065 |
rs768861188 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795968 | AGAATAATTTTCTAA[C/T]GCATCTCTGGTGATC | 254065 |
rs768864680 | snp | C/T | 2.56693e-05 | 0.00358246 | intron-variant | BRWD3 | GRCh38.p7 | X:80690125 | CTCTGTTAGCCTTGG[C/T]TAATATATTTAAAGT | 254065 |
rs768868341 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733088 | TGAGCCAAGATCGCA[C/T]CACCGCACTCCAGCC | 254065 |
rs768872989 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726854 | CAGAAAAAGTTATTT[A/C]TTTGTTATAACAAAA | 254065 |
rs768873501 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749446 | TATCATTACATATGA[C/T]GTTTTTTGTCACTAT | 254065 |
rs768929443 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718749 | AAAATGCAATGTTAC[A/T]CAGATAAATGACTCT | 254065 |
rs768944259 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684491 | ACCCCAGCACACTGT[C/T]TAATGATAAAAGATG | 254065 |
rs768953675 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721538 | TCAGTAACTTACTAG[A/C]TCATACCTGAAGACA | 254065 |
rs768956020 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726217 | GTTATATGTCTGTAT[A/G]ACATATAACACGTTT | 254065 |
rs768966291 | snp | A/C | 2.39057e-05 | 0.00345721 | intron-variant | BRWD3 | GRCh38.p7 | X:80725099 | TATTAACAATGAAAG[A/C]AACACGAAATGTTTG | 254065 |
rs768993723 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738453 | ACCACTTTAACTATA[-/T]TTTTGTTAAAAAAAA | 254065 |
rs769018623 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802536 | CATCTGGGGTCATAG[C/T]TCTCCAGATTTCCAT | 254065 |
rs769039470 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792918 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCTGAGG | 254065 |
rs769106408 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778252 | TTTGGGGGCTAGGAC[A/T]AAAACATTATTACCA | 254065 |
rs769112005 | snp | A/G | 4.79214e-05 | 0.00489473 | intron-variant | BRWD3 | GRCh38.p7 | X:80704887 | ACCTAAGTATAGAAA[A/G]GGAGTAGTTTTACTT | 254065 |
rs769128712 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80701317 | CTTTGGGAGGCCGAG[A/C]TTGGTGGATCACCTG | 254065 |
rs769138541 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740898 | CCAATATTCAAGTTA[C/G]AACCTGTTTATATTC | 254065 |
rs769179265 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685252 | CATAAAAAAGTAAAC[A/G]TTTACAAGGAGGATA | 254065 |
rs769196998 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80738399 | AGAAAAAAAGTAACA[C/T]GTAATTCTGCCATTC | 254065 |
rs769203629 | snp | A/C/T | 9.92928e-05 | 0.00704544 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704647 | AAAAACAAAAAATAA[A/C/T]AAAAACAAAATAACT | 254065 |
rs769215888 | in-del | -/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675422 | ACAGCTGTTAAATGG[-/T]TAAGTGGAGCAGAAA | 254065 |
rs769222181 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80761390 | AGATTATTAGACCAA[A/C]ATAAAAAGACCCACA | 254065 |
rs769229323 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681058 | CAAGTGATCCTCCCA[C/T]CTCAGCTTCCTAAAG | 254065 |
rs769233135 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769608 | GTGTGTAGAGGGAAA[C/T]TTACAGCACTAAATG | 254065 |
rs769240720 | snp | A/C | 5.36157e-05 | 0.00517735 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80689821 | TTTTATTATAAGTAT[A/C]CAGTATATCAGTACA | 254065 |
rs769243593 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729839 | TTATTAATGTAAAAA[-/G]ATATTTTATATTCAC | 254065 |
rs769269948 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711582 | AAAAGTCTGGCACTT[G/T]TATTTAAGTCTGAAA | 254065 |
rs769276200 | snp | A/G | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811695 | CCTCAGCACTTTTAC[A/G]TGCTTACCTCATTTA | 254065 |
rs769294614 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698412 | CAACAAGGTTAGGAT[A/C]AAAAGTAAGAACTTG | 254065 |
rs769297909 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80803355 | ATCCAAAGTATTAGT[C/T]CCTAACACCAGCTCT | 254065 |
rs769299630 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762424 | AGCTGCTGCTGAGTG[C/T]TTCATGTTTAAATAT | 254065 |
rs769327320 | in-del | -/TTTTG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748620 | ATTCTGAGTCTTTTC[-/TTTTG]TTTTTTTTCCTAAGT | 254065 |
rs769336351 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689136 | TTGTTTTCCAGTAAA[A/G]ATTTGTGAATTATCA | 254065 |
rs769337078 | snp | C/T | 6.93505e-05 | 0.00588816 | intron-variant | BRWD3 | GRCh38.p7 | X:80728939 | AGTATTCATATCTTA[C/T]AAATTTTTGACAAAG | 254065 |
rs769341061 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781854 | CACTGATGAAAGAAA[C/T]TGAAGATACAAAAAA | 254065 |
rs769343648 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754203 | TTCCTAAGTGTTCTG[G/T]AGTTTTCTATGTAGA | 254065 |
rs769363805 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673232 | CATCTGCGGGAAACA[A/C]AGTATTATAGAGAAG | 254065 |
rs769366505 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80696828 | GGGTGGGCCAACCTC[A/G]TATTTGATTCCTACA | 254065 |
rs769370426 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801052 | GTGCTCAGTAGAGAA[A/G]AGTCCAACAAAAGAA | 254065 |
rs769394988 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731357 | GAAAAAGACAGGGAG[C/T]TAAAAATTTAGGTTC | 254065 |
rs769398203 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769150 | TAAGAATGGCAGACT[C/T]TAACACCCCACTGTC | 254065 |
rs769422590 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722858 | TTGTTTTCATTCCTT[A/G]AGCACACTCATTTTT | 254065 |
rs769422669 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729768 | CAACAGTAACGAAGA[C/T]TTGCTTAGAGGCTGT | 254065 |
rs769425645 | snp | A/C | 2.33987e-05 | 0.00342035 | intron-variant | BRWD3 | GRCh38.p7 | X:80691031 | TATAAATTTTATAAT[A/C]AGTGATTAAAAAAAA | 254065 |
rs769429634 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772430 | CAATGAGAACACCTG[C/G]ACACAGGGCGGGGAA | 254065 |
rs769435592 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751527 | ATGGCCAAAGAAACA[A/C]AGCTAAGTACATAAG | 254065 |
rs769439207 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701254 | TTCCTCAAGTTTAAA[A/G]GCAGTGATAGAGGCT | 254065 |
rs769446425 | in-del | -/CAAAGTAACAGAAAATCAAGAAGAAAAC | 2.29806e-05 | 0.00338966 | intron-variant | BRWD3 | GRCh38.p7 | X:80716270 | TAACAAGTCAAAGGT[-/CAAAGTAACAGAAAATCAAGAAGAAAAC]CAATCATTTAAGAAT | 254065 |
rs769459974 | snp | C/T | 2.46469e-05 | 0.00351039 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80730017 | TCCACTAACAAATCT[C/T]AAACTAGAAAGAGTT | 254065 |
rs769465652 | snp | C/T | 3.29658e-05 | 0.00405978 | intron-variant | BRWD3 | GRCh38.p7 | X:80707532 | CCAGCAATTAAGATA[C/T]ATGGATATTACCAGC | 254065 |
rs769512589 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80679748 | GAAACTAAAAAAAGA[C/T]GCTAGTTGGCCACTG | 254065 |
rs769542738 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773095 | TCACGCAGGAGGGAA[A/G]CCGATGTGGTTATAA | 254065 |
rs769543054 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808511 | TGGTGAAAGAGTTAG[G/T]TTAAGTTGAAATGAA | 254065 |
rs769544155 | in-del | -/C | 3.04627e-05 | 0.00390262 | intron-variant | BRWD3 | GRCh38.p7 | X:80743988 | ATCAGAGAATTCTCA[-/C]CTTTTTTACATATGT | 254065 |
rs769548803 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764678 | GAAAATTGGTAAACA[A/G]GGTGTCATCAAATTT | 254065 |
rs769562865 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734678 | CTAAAATGATAAAAT[G/T]TTAGGTTCTGTATAT | 254065 |
rs769579138 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80742035 | CTTCTAGGGTTTTTA[C/T]GGTTTCAGGTCTAAC | 254065 |
rs769602438 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778547 | ACTGTTCATAGATCA[A/G]GCTTCTTGTACCATA | 254065 |
rs769608706 | snp | A/G | 2.32593e-05 | 0.00341015 | intron-variant | BRWD3 | GRCh38.p7 | X:80808628 | AAAAGAAAGGGGGAA[A/G]CGGAGGCAAATGATG | 254065 |
rs769617234 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723540 | ATCTTCATCACCCTA[C/T]AACTTATCTCTATTG | 254065 |
rs769618856 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788198 | ATCCCAGGGGGAGGC[A/C]GAGGCAGGTGATTGC | 254065 |
rs769624612 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733514 | AAGACATGAAACAGA[C/T]TTTTCGTTAAAATGG | 254065 |
rs769625370 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80807623 | ACACAAGGGAACCTC[C/T]CCCGCAAAATAAAAA | 254065 |
rs769637442 | in-del | -/A | 0.0158009 | 0.0874689 | intron-variant | BRWD3 | GRCh38.p7 | X:80800760 | CAGGGGAAAAAAAAG[-/A]AAAAAAAAGACAGCA | 254065 |
rs769662496 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80680540 | ACTTTGTGATATAGC[A/G]GGCCCCTAAGGAAGA | 254065 |
rs769664748 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713827 | ACTCTGCTCTTTTGT[G/T]ATTCTCTTGCTCAAA | 254065 |
rs769668028 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797877 | GAGGCGGATGGATCA[C/G]AGGGTCAGAAGATGG | 254065 |
rs769680542 | snp | A/G | 7.30256e-05 | 0.00604214 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695953 | TATAAAACTGATGTA[A/G]CACAAGGAAGTCAAT | 254065 |
rs769687149 | snp | A/G | 2.4173e-05 | 0.00347648 | intron-variant | BRWD3 | GRCh38.p7 | X:80717776 | TAAAACAAAAACAAG[A/G]AAAATTATCACTTTG | 254065 |
rs769690356 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707254 | AAGGCCCACAGTGAC[A/G]TCAGAAAGGTATTGG | 254065 |
rs769738954 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724316 | TTTGGGTCTATATAA[A/T]GCATATAAAAGTAAA | 254065 |
rs769742076 | snp | C/T | 2.70918e-05 | 0.00368038 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80689787 | TCTGCATCAGTACTG[C/T]TTCGTTCTTCTGCTT | 254065 |
rs769749780 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725942 | TAACTTGTTTACATG[C/T]TACATGTCTATATAA | 254065 |
rs769759853 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789035 | ACTTATTGAACTGCA[C/T]ACTTAAAAAGACAGC | 254065 |
rs769762741 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735329 | GAACGTGGTCAATAA[G/T]TACTATTCTCATCAA | 254065 |
rs769769411 | snp | C/T | 2.28329e-05 | 0.00337874 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692944 | AACATACTTACTGAA[C/T]ACTGTAACACTGGAA | 254065 |
rs769778027 | snp | A/G | 2.28715e-05 | 0.0033816 | missense, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793627 | AAAATCTCACCTTTG[A/G]CATCCCGTAGCAGAG | 254065 |
rs769797224 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712542 | GGCCTCCCAAAGTGC[C/G]GAGATTGCAGCCTCT | 254065 |
rs769802300 | snp | A/T | 2.55601e-05 | 0.00357483 | intron-variant | BRWD3 | GRCh38.p7 | X:80682672 | ACTAGTTTTATATTT[A/T]AAAAAAAGGTATAAA | 254065 |
rs769804245 | snp | C/T | 2.51225e-05 | 0.00354409 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80696831 | TGGGCCAACCTCATA[C/T]TTGATTCCTACAATC | 254065 |
rs769810425 | in-del | -/TAAT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757147 | AAGTTTTAGTATATA[-/TAAT]TAGTTACTTTGATTA | 254065 |
rs769833647 | snp | G/T | 4.56965e-05 | 0.00477977 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704786 | TCTGGTTTGTCTTTT[G/T]GGGGGTTGTAAATTT | 254065 |
rs769838622 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763693 | ATATGCACAGTATCT[C/T]TATCCTGGAAATTAC | 254065 |
rs769849363 | in-del | -/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670340 | CACAGGCTCAATATA[-/T]TGGTTTTATTTTGCA | 254065 |
rs769857791 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712947 | GTGAGGAGCTCCTCC[A/G]CCCGGCACCCACCCC | 254065 |
rs769863318 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798522 | GTCATTTAACTACAT[C/T]TATCTCTCTGGAATA | 254065 |
rs769882706 | in-del | -/A | 0.000239292 | 0.0109357 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704637 | TCAAAGGCAAAAAAC[-/A]AAAAAATAACAAAAA | 254065 |
rs769887098 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810207 | GAGGAACTTAAGAGA[C/T]GGTGTTTTGACTCGA | 254065 |
rs769892904 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786054 | AAAAGAAAATCAAAT[G/T]TGTAAAATAAGTAAA | 254065 |
rs769893810 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80677886 | GGAATGTATTTTAGA[C/T]AGGGAAGACTTCTCT | 254065 |
rs769897609 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721445 | AACCTTTATGAGCAA[G/T]AACATAAAAGGACGT | 254065 |
rs769902897 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80731882 | CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 254065 |
rs769913665 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80795368 | ACACACACACACACA[C/T]GTGTATATATACACA | 254065 |
rs769916308 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777437 | TCACTCTGTCACCCT[C/G]ACTGTAGTGCAATGG | 254065 |
rs769919350 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749229 | AATGTTTCCTTATTG[A/C]TTTTCTGTCTACATA | 254065 |
rs769939943 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764328 | TTTTTTTTTTAGAGA[C/T]GGAGTCTCGCTCTGT | 254065 |
rs769952374 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746173 | ATCCACCATATGTAT[A/G]ACTGCCCCTAAAAAT | 254065 |
rs769954008 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687817 | ATATGTGACCCCTCA[C/T]AGGGGAAAGATAATA | 254065 |
rs769966904 | snp | C/T | 2.28616e-05 | 0.00338087 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676966 | TCTTCCTCTGCCTCC[C/T]CTACTCCATCTACCC | 254065 |
rs769980542 | snp | C/T | 2.29082e-05 | 0.00338431 | intron-variant | BRWD3 | GRCh38.p7 | X:80688040 | AAACCTGAAAACATA[C/T]CTCCTCAGCAGTTCA | 254065 |
rs769980652 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770913 | GCAAAGTCTCAGGAT[A/G]CAAAATCAATGTGCA | 254065 |
rs769994317 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740058 | ATAATCTCCCAAATC[-/A]AAAATGCATGAAATA | 254065 |
rs770015241 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801340 | ATTCTCCTGCCTCAG[A/C]CTCTGGAGTAGCTGG | 254065 |
rs770061632 | snp | A/G | 4.57383e-05 | 0.00478195 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682014 | GGAGATGAGAAAGGA[A/G]AGCTAGTCCTGGCAT | 254065 |
rs770073954 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725962 | TGTCTATATAACACA[C/T]AACATGTTTACATGT | 254065 |
rs770102705 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739164 | AGAGGTCATGAGAAT[A/T]TGCCAGATTCTAGAT | 254065 |
rs770125740 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678904 | AGGGAGGTAATTAAG[A/G]TTAAATGAGGTTATA | 254065 |
rs770126875 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680803 | TTTTTCTCCCAATTC[A/C]TTTTATTTTATTTAT | 254065 |
rs770156443 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810668 | CTATCTCTATGCAAG[C/G]TATCAATAGTTTTCT | 254065 |
rs770166982 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80691542 | ACCCATCCAAAGTCA[A/G]GCTCAGGAATAGCTA | 254065 |
rs770168569 | in-del | -/AA | 0.00159067 | 0.0281568 | intron-variant | BRWD3 | GRCh38.p7 | X:80745123 | ACCAGTACTGAAACC[-/AA]AAAAAAGATATAAAA | 254065 |
rs770176980 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733047 | AGGCAGGAGAATCGC[C/T]TGAACCCAGGAGATG | 254065 |
rs770186970 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80737587 | CACCTGTAATCTCAG[C/T]ACTTTGGGAGGCCGA | 254065 |
rs770252775 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682801 | TAAAATAAATGTTTT[C/T]CAAATATAGTATTCA | 254065 |
rs770276714 | snp | G/T | 3.48639e-05 | 0.00417501 | intron-variant | BRWD3 | GRCh38.p7 | X:80703638 | TATAAAACACAGTTC[G/T]CCAATACATAAAACA | 254065 |
rs770284068 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80790835 | AATTCAATATATTAA[G/T]TATGACTAAAGCTTT | 254065 |
rs770290513 | snp | C/T | 0.000101179 | 0.0071119 | intron-variant | BRWD3 | GRCh38.p7 | X:80709397 | TGGGAAACAAAAAAC[C/T]ACATCAAATAAATAA | 254065 |
rs770291379 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80737380 | TATACTATATTACTT[A/G]AGGGATAATGACAAG | 254065 |
rs770322444 | snp | A/G | 4.48189e-05 | 0.00473365 | intron-variant | BRWD3 | GRCh38.p7 | X:80745743 | CACTGAAAAAAATAC[A/G]AAATTAACTTAAAAC | 254065 |
rs770323344 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80759115 | ATCAGGAAACTACAC[-/T]TCTACGAATGAAGGT | 254065 |
rs770347362 | snp | A/T | 0.000123579 | 0.00785965 | intron-variant | BRWD3 | GRCh38.p7 | X:80709616 | TTTTAAAAAAGGAAA[A/T]GCTCAGTAAACACAC | 254065 |
rs770355049 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80768916 | GGAAAGCAAAAAAAA[A/G]AAAAAAAAAAGCAGG | 254065 |
rs770367953 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721294 | AATAAAGTCTGATAA[A/G]TTAGACTTTCTTATT | 254065 |
rs770378470 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684244 | GGTATCACCTACTAC[A/G]ATCCACCATGAAATA | 254065 |
rs770387879 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774740 | CTTTTATGTCCTGTA[C/T]CCAACCAAACTGTAT | 254065 |
rs770393501 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718344 | ACACAAATGGAAACT[A/G]AAACATCCAACTGTT | 254065 |
rs770438693 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776859 | TTGCCTCAGTTAACA[C/G]CCACCAATCTAGAAC | 254065 |
rs770446450 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768787 | AGACACAGACTGGCA[A/G]ATTGTATAAAGAGTC | 254065 |
rs770450843 | snp | C/G/T | 0.000137995 | 0.00830552 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682628 | GCATCATGCTATAGA[C/G/T]CTGAGAAGGCAGAAA | 254065 |
rs770461632 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80717094 | TATTACAGCAAATGT[C/T]AGGGTTTACAAATAT | 254065 |
rs770466015 | snp | A/G | 2.30407e-05 | 0.00339408 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793591 | CCACTCCTTCCTCTG[A/G]TATCACAGTCCTAAA | 254065 |
rs770481938 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684334 | GCTCATAAAAACAGC[A/G]TAAGTCTGTGGGAAA | 254065 |
rs770492420 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696225 | GTTTATAAACCTTAA[G/T]ATGAGGTATTTTATA | 254065 |
rs770498149 | snp | A/G | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809759 | GAGAGAGAGAGGAAA[A/G]AGAGAGAGAGAGAGA | 254065 |
rs770504757 | snp | A/G | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811149 | TTGGTTGTTATTGCC[A/G]TGGAACTTGACAAAA | 254065 |
rs770550374 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767620 | CAGAGCAGAAAAGCT[G/T]AAAATTCTAAAAACC | 254065 |
rs770560510 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699691 | AAAAGTTGCTGATTA[C/T]GGAAAATATCCACAA | 254065 |
rs770563163 | snp | A/G | 3.07305e-05 | 0.00391973 | intron-variant | BRWD3 | GRCh38.p7 | X:80707377 | CGAGAACATAATTTC[A/G]TATTAAAACTGTTCA | 254065 |
rs770563580 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737277 | TTTGCAGATAACATA[C/T]GTACATCCTCCTGTA | 254065 |
rs770564624 | snp | A/G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80723523 | TCCTAAGGAATGTTT[A/G/T]TATCTTCATCACCCT | 254065 |
rs770575500 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759988 | CACTGCTAATCCTCA[C/T]CTTCCAATTAAATCT | 254065 |
rs770581995 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736603 | TATATAATTTTGTCT[C/T]TTTTAGATGTAAGCC | 254065 |
rs770587169 | in-del | -/TTTCTT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807481 | TCATACACCGCCAAC[-/TTTCTT]TAACTTTGTCCGATT | 254065 |
rs770588783 | snp | C/G | 2.30208e-05 | 0.00339262 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80808587 | CTCCCAATCTAAGCG[C/G]CGCGGAATCAGCTGG | 254065 |
rs770615602 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708177 | AAGGCAGGCAGATCA[C/T]CTGAGGTCAGGAGTT | 254065 |
rs770618018 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80790728 | CACATGTGACCCATG[A/T]AGCATAACACACTAC | 254065 |
rs770622556 | snp | A/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716194 | TTTTTCTTCTTTTCA[A/T]CTGTATAAAGACTGA | 254065 |
rs770627138 | snp | A/G | 2.44963e-05 | 0.00349965 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695936 | CCTTTCTTTGGCTTC[A/G]TTATAAAACTGATGT | 254065 |
rs770633450 | in-del | -/ATAAGGTAGCT | 2.47103e-05 | 0.0035149 | intron-variant | BRWD3 | GRCh38.p7 | X:80691195 | AATTATGAAAATCAA[-/ATAAGGTAGCT]ATAAAGGACATTAAC | 254065 |
rs770636361 | snp | A/G | 2.40999e-05 | 0.00347122 | intron-variant | BRWD3 | GRCh38.p7 | X:80725110 | AAAGCAACACGAAAT[A/G]TTTGGTTCATTTGGT | 254065 |
rs770668648 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782587 | ATTTACAAAGTATCC[A/T]TCTGACAAAGGATCA | 254065 |
rs770683858 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80710390 | TTGACTACAGAGCTA[C/G]GTCCACTGGGGCCCA | 254065 |
rs770688181 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688207 | CATTTACAAATAAAC[A/G]GGAAATAAAATCACA | 254065 |
rs770688493 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778958 | CAGCCAAGATGGTGC[C/T]ATTGCACTCCAGCCA | 254065 |
rs770696972 | snp | C/T | 2.29632e-05 | 0.00338837 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676946 | CTCCCTCGTCCCCTG[C/T]CTCCTCTTCCTCTGC | 254065 |
rs770701748 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713503 | GGCAGCATGCTCCTT[A/G]AGAGTCATCACCACT | 254065 |
rs770703111 | snp | C/G | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80741284 | ATGGTGTATATGTGC[C/G]ACATTTTCTTAATCC | 254065 |
rs770713485 | snp | A/G | 2.31431e-05 | 0.00340162 | synonymous-codon | BRWD3 | GRCh38.p7 | X:80676732 | ATTGTCATTATCAGA[A/G]TCATCATTATATAAA | 254065 |
rs770713512 | snp | A/G | 4.57928e-05 | 0.0047848 | intron-variant | BRWD3 | GRCh38.p7 | X:80692918 | TGTCATATTAGGCAT[A/G]AAAGATCATAAACAT | 254065 |
rs770728143 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770254 | CAACTCATTTTATGA[A/G]GCCAACATCAGCTTG | 254065 |
rs770738763 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802619 | TTGCACAGCATTTTA[A/C]AATTAACAAAATGCA | 254065 |
rs770783411 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796572 | CATGAGTGAATCACC[G/T]GTGATTATTTTTGTT | 254065 |
rs770795946 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710286 | CAACACAACAATATG[C/G]CTGGAGACCATATGG | 254065 |
rs770814045 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733897 | ATCATTTATTTAATT[A/C]TTTTCCAATGGAATC | 254065 |
rs770825677 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706400 | AGAAGTGAGCCACCA[C/T]GTTCGGCAAATTTTT | 254065 |
rs770832206 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80713781 | TCTACATACAAAAAG[A/T]AACAATTTAATTTTT | 254065 |
rs770833264 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731052 | ATATCTTTGCTGAGT[C/G]AGAGTAGGTGTATTT | 254065 |
rs770892634 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771879 | AAAATGCTCATCATC[A/G]CTGGCCATCAGAGAA | 254065 |
rs770894322 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80797760 | TTGCTCGATTTCTAA[C/G]CAGTTACATTGAAAA | 254065 |
rs770894577 | snp | A/G | 2.32315e-05 | 0.00340811 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735169 | GGACTCCAGGTCTGG[A/G]TCTCTCAGTAAATTT | 254065 |
rs770919799 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80705366 | CAAGGATTATAATTA[C/T]AATGCTTAGTTTCCT | 254065 |
rs770923318 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80765662 | TGCTTTCCTTTATCA[C/T]GTAAAATAAGATGTA | 254065 |
rs770923430 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80680316 | TTGATGTCCCTTGTA[C/T]GGTCCAAGATAGACG | 254065 |
rs770938787 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80719939 | AAAGATAAACCACAT[A/G]TACGACGGTAGTCTC | 254065 |
rs770945979 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751464 | GAAAATAAATAACTA[C/T]CAGAAAGAAAATCCA | 254065 |
rs770958698 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80686207 | ACGCATAGGTGGGAA[A/T]TGAACAATGAGAACA | 254065 |
rs770966518 | snp | A/G | 4.58784e-05 | 0.00478927 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686913 | GCTCCGAGTCTTCAC[A/G]TTCATAAATGAGGCT | 254065 |
rs770991642 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80677530 | ATATTAAAGTGTTTA[-/T]TTTTGTCTGCTTTTT | 254065 |
rs770992058 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768796 | CTGGCAAATTGTATA[-/AA]GAGTCAAGACCAATC | 254065 |
rs770994726 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728582 | CTTTTAGCAGGTATA[A/G]CGCGTGTCATCCCTA | 254065 |
rs771017032 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80764531 | TGTTAGCCAGGATGG[G/T]CTCGATCTCCTGACC | 254065 |
rs771019337 | snp | C/T | 6.85464e-05 | 0.00585393 | intron-variant | BRWD3 | GRCh38.p7 | X:80717556 | ATTTTTTTCTAAATG[C/T]TACCTTATTGACTCA | 254065 |
rs771057332 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794325 | AGCCTGGGCCACACA[A/G]CAAAACCCCATCTCT | 254065 |
rs771073013 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762739 | TACAGTATTGAAAAA[A/G]GAACAAGTGGCCAAA | 254065 |
rs771078317 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779272 | GTGAGTCGAGATTGT[A/G]CCACTGCACTCCAGC | 254065 |
rs771085989 | snp | C/T | 2.1324e-05 | 0.0032652 | intron-variant | BRWD3 | GRCh38.p7 | X:80809416 | TTCCCTTAGCACCCC[C/T]CCACCCCCCGACACA | 254065 |
rs771088472 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747507 | TACCAATAGAAGGGG[A/G]AAAAAAAAACAAAAC | 254065 |
rs771093240 | snp | C/T | 2.62719e-05 | 0.00362426 | intron-variant | BRWD3 | GRCh38.p7 | X:80687052 | CTTTCCTTAACTCAG[C/T]TGATTTTCTCATAAG | 254065 |
rs771096487 | snp | A/G | 5.67601e-05 | 0.00532699 | intron-variant | BRWD3 | GRCh38.p7 | X:80703475 | TTATAACAGGTAATA[A/G]TTACCTCATCTCCCA | 254065 |
rs771097745 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763056 | GCCCAGAGTCTATGA[C/T]ATATTTTTTAAATCC | 254065 |
rs771101941 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739950 | AGATAAGGGGGACTA[C/T]GATAATCAAATGATT | 254065 |
rs771105438 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80780724 | TTATGAGAGTACAAA[C/G]AGGAGGAAGGTGGTA | 254065 |
rs771109276 | in-del | -/A | 6.30597e-05 | 0.00561479 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80791989 | GCTAAGGAATAGAGC[-/A]AGTTTTTTTTTTAAC | 254065 |
rs771125505 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748088 | CCTCAGATGATTCGC[C/G]CACCTCAGCCTCCCA | 254065 |
rs771143868 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80747205 | ATTACTTCTGCTTGG[A/C]TTTTGTCTCTTCATA | 254065 |
rs771144043 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758026 | CCAACACGGTGAAAC[C/T]CCGTCTCTACTAAAA | 254065 |
rs771156395 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790472 | TCTAAAAGCTCCTCC[A/C]CAAATAACATGCCAG | 254065 |
rs771158990 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764572 | CCTGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 254065 |
rs771164748 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770235 | AAAAAGAGGGAAACC[C/T]CCCCAACTCATTTTA | 254065 |
rs771165731 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774305 | AGGGTCTTGCTCTGT[C/T]ACCCAGGCTGCAGTG | 254065 |
rs771173711 | snp | C/T | 0.000114294 | 0.00755868 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681422 | TTCGGCTATATCCAC[C/T]GAAGCTCGATGAAGA | 254065 |
rs771212389 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731820 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 254065 |
rs771243415 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676016 | AACTGTAGTATAAAT[A/C]TATACTTCAGTTCAG | 254065 |
rs771250492 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80712797 | GCATCTCTGCCCGGC[C/T]GCGACCCCGTCTGGG | 254065 |
rs771269516 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80752980 | GATCATTTTTTTGTA[C/T]ACCTGTTGGCCATTT | 254065 |
rs771321216 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732882 | TGGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT | 254065 |
rs771338084 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712415 | CTCGGCCTCCCGAGG[C/T]GCCGGGATTGCAGAC | 254065 |
rs771338843 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763496 | TAGGCCCTAAGAAGA[C/T]GTTTAAAAACTACTA | 254065 |
rs771362958 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701683 | GGTCAGAATTTCTAA[C/T]AGCTAAAAATTTGAG | 254065 |
rs771373177 | snp | C/T | 0.000126444 | 0.00795021 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703492 | TACCTCATCTCCCAT[C/T]TGTGGGACAAATGGG | 254065 |
rs771399121 | snp | G/T | 2.45794e-05 | 0.00350558 | intron-variant | BRWD3 | GRCh38.p7 | X:80722830 | CATACACAGGGAATT[G/T]ATAAGTAAATACTTG | 254065 |
rs771409359 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80682733 | TACAGACAAAATATC[C/T]GTTCACTTGAAAAAT | 254065 |
rs771423184 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715859 | GTTTTACATTCTAAT[G/T]AGTGATCTGGTAATA | 254065 |
rs771431692 | snp | A/G | 9.16853e-05 | 0.0067701 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744077 | CTGAAGGACTGCAAC[A/G]GGTGCACAAGTTCGA | 254065 |
rs771447529 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80692830 | ACAGGTACAGGTATT[A/G]TGAGACTAGATAAGT | 254065 |
rs771451483 | in-del | -/A | 0.000142454 | 0.00843839 | intron-variant | BRWD3 | GRCh38.p7 | X:80691039 | TTATAATAAGTGATT[-/A]AAAAAAAACAGACCT | 254065 |
rs771467115 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785098 | AAGTTTCTAAAATGA[A/G]TATTAATCTTTAAAA | 254065 |
rs771472214 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735506 | GATTTTCTATATAAA[C/T]TGTCTCTTCAACATT | 254065 |
rs771474812 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80693190 | AGGTTTTCGGGATAA[A/G]TGATTATTTTACATT | 254065 |
rs771475202 | snp | A/C | 2.28141e-05 | 0.00337736 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744188 | TTCAGCAGAGTGTCC[A/C]CGAAGTGTAGCAAGA | 254065 |
rs771475845 | in-del | -/AA | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80725956 | GTTACATGTCTATAT[-/AA]CACATAACATGTTTA | 254065 |
rs771477661 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80715953 | AATGACCACATGTCC[C/T]AGATTTGGGGGGACA | 254065 |
rs771487426 | snp | A/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675825 | GGGAAACTTTTGCAT[A/T]TGGCACCTTGTCTAG | 254065 |
rs771497157 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80774276 | TTTTTTTATTTTTTA[-/T]TTTTTTTTGAGACAG | 254065 |
rs771526910 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810097 | TTGGAACTCTGTGGT[A/G]GCATTCGCGTCTGCG | 254065 |
rs771527105 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80774209 | TTTTGTTCTATCCTG[A/G]CCCACCTTTATTGAA | 254065 |
rs771549282 | snp | C/T | 2.28564e-05 | 0.00338048 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682034 | AGTCCTGGCATGAGA[C/T]ACTGAGGTATTCTGG | 254065 |
rs771553480 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80738945 | TGAAGACTTCAGCTT[C/T]AACTCTGAGATTGGA | 254065 |
rs771553689 | snp | A/T | 4.27771e-05 | 0.00462458 | intron-variant | BRWD3 | GRCh38.p7 | X:80692015 | AAAAATTAGAAAAAA[A/T]TATTTTCCAATATCA | 254065 |
rs771555170 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715709 | TGTCTTACAGCCTGA[A/G]AGCAACCACATACAA | 254065 |
rs771564048 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806116 | CTTCTGTTCAAATTA[C/T]CACTCAACCCTGCCC | 254065 |
rs771572074 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758186 | TCAGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 254065 |
rs771588941 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784730 | ATCCCATTCCTTTTA[C/T]ATGGCTGCATAGTAT | 254065 |
rs771591325 | snp | C/T | 2.4173e-05 | 0.00347648 | intron-variant | BRWD3 | GRCh38.p7 | X:80692185 | TGCAAATCAAATTAA[C/T]CATATAGTACTTCCT | 254065 |
rs771595677 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698653 | GGCGGAGGTTGCAGT[A/G]AGCCGAGATCGCTCT | 254065 |
rs771601726 | snp | C/T | 4.67388e-05 | 0.00483396 | intron-variant | BRWD3 | GRCh38.p7 | X:80745548 | CTATATATGTTACCA[C/T]ATTATAAATTTTACA | 254065 |
rs771622375 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795025 | TAAATACTATGCTTT[A/C]AATAACTCAGCTATG | 254065 |
rs771640314 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714983 | TAACCTTTACAAATA[C/T]AAAACATTACTATTG | 254065 |
rs771659765 | in-del | -/AT/ATAT | 0.0271702 | 0.113344 | intron-variant | BRWD3 | GRCh38.p7 | X:80686424 | TTAAAGTATAATAAA[-/AT/ATAT]ATATATATATATATA | 254065 |
rs771674129 | snp | C/T | 0.00011411 | 0.0075526 | intron-variant | BRWD3 | GRCh38.p7 | X:80682459 | GTTGCATCAATGTAA[C/T]GATACCTAGGTGCTC | 254065 |
rs771682930 | snp | A/T | 6.87655e-05 | 0.00586328 | intron-variant | BRWD3 | GRCh38.p7 | X:80717541 | AGAATAAAGCTTTAA[A/T]TTTTTTTCTAAATGT | 254065 |
rs771689301 | snp | A/G | 4.62492e-05 | 0.00480858 | intron-variant | BRWD3 | GRCh38.p7 | X:80724889 | GTTATTATATGAGAG[A/G]AGTTGGTTTTAATGT | 254065 |
rs771696672 | snp | C/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669200 | AAAAACTTGTCGTTG[C/T]GTTCAGCAGTCTTAA | 254065 |
rs771697784 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80743950 | TTATTCTTTGGGCTA[C/T]TATCTATACAATGTA | 254065 |
rs771698893 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80728584 | TTTAGCAGGTATAGC[A/G]CGTGTCATCCCTATT | 254065 |
rs771705420 | in-del | -/G | 3.30868e-05 | 0.00406723 | intron-variant | BRWD3 | GRCh38.p7 | X:80681546 | ATTATCATGTTTTCA[-/G]GGAAAGTTAAACAGG | 254065 |
rs771714280 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743077 | TACATCCCATGAATA[C/T]CTAATTTATTGAGAG | 254065 |
rs771720430 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804863 | TAGGAAGCAGAAAAT[-/AA]AGTGCCCAGATGAAA | 254065 |
rs771731978 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80709314 | ATGAACAAATCTCTT[A/T]TAAGAATATAATTAA | 254065 |
rs771750517 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789668 | GGCGTGAGCCACCCC[A/G]CCTGGCCTCCATGCT | 254065 |
rs771767693 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670559 | CCTGGGACTTACAGG[C/G]ACACACAACCATGCC | 254065 |
rs771767698 | snp | C/T | 9.12554e-05 | 0.00675421 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682478 | ACCTAGGTGCTCCAC[C/T]ACTAGATAATGAACT | 254065 |
rs771784434 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721680 | GCTTATTCCAATGTT[G/T]TATTCTACTATCTTC | 254065 |
rs771787486 | snp | A/G | 1.70848e-05 | 0.00292269 | intron-variant | BRWD3 | GRCh38.p7 | X:80745762 | TTAACTTAAAACTTA[A/G]AAGTGAAACTGATTT | 254065 |
rs771801439 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736384 | TTTTTAATCACTTTC[A/G]GTGGAGAATAAACTC | 254065 |
rs771822280 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807520 | CTCCACTTGGATCTT[A/T]CTTGAAGGAAAGATA | 254065 |
rs771824475 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80698240 | ATTTACTGATTATTA[A/G]TCACATTTAACAGAT | 254065 |
rs771835323 | in-del | -/GA | 0.285075 | 0.247527 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809823 | GGGGGTGGGGGGGCG[-/GA]GAGAGAGAGAGAGAG | 254065 |
rs771841979 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678732 | CGGTAGGAAACAAGA[A/G]AGCAGACTGGAAGAA | 254065 |
rs771850069 | snp | A/C/T | 0.00013764 | 0.00829475 | synonymous-codon, missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716157 | TAAAACTATACTTAC[A/C/T]CTTTGAGTAGTGTAA | 254065 |
rs771857019 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687298 | CTTTCCTCTACAACA[A/T]CAAGTTATAGAGCCT | 254065 |
rs771883586 | in-del | -/GTAA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765576 | ATAGAACTGAGTACT[-/GTAA]GTGTTATGAAATATT | 254065 |
rs771907756 | snp | C/T | 9.16758e-05 | 0.00676975 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686896 | AGCTGGCTGTCGAAA[C/T]GGCTCCGAGTCTTCA | 254065 |
rs771913142 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759019 | GTCTCTAGTTTATCA[A/G]TGTCTGAGCCTTTTA | 254065 |
rs771916697 | snp | C/T | 0.124138 | 0.216007 | intron-variant | BRWD3 | GRCh38.p7 | X:80708394 | GAACAAGACTCTTGT[C/T]TTTTTTTTTTTTTTT | 254065 |
rs771916762 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782937 | ACCAGAATGTAAAAG[A/G]AGCTCAAACAACTCA | 254065 |
rs771919466 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805895 | AGCCGAGATCCCGCC[A/T]CTGCACTCCAGCCTG | 254065 |
rs771923919 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80694225 | TGTTGGGCCTACAGA[C/T]GCATAGAAGTCAAGA | 254065 |
rs771926309 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727927 | CATGACAGGACTCTG[A/T]CTAATTTACCATTTA | 254065 |
rs771949498 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699422 | CTGTATGTGCATGTG[C/T]GCATATATATATACA | 254065 |
rs771964354 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80713499 | TGAAGGCAGCATGCT[C/T]CTTAAGAGTCATCAC | 254065 |
rs771967343 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748341 | CTCAAAAGGGATATT[A/G]GCCTTTAGTTTCCCT | 254065 |
rs771985128 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710225 | TCTGATAGACCACTT[C/T]CTGTGTCTTCTCTTG | 254065 |
rs771992989 | in-del | -/AT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795425 | CAGTGGTATATACAC[-/AT]ATGTATATATACACG | 254065 |
rs772011607 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762503 | AGCGGTGAACTCCTC[C/T]TCATTTTTCTGGGTG | 254065 |
rs772014147 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807347 | CGGTAGACTTGATAA[C/T]AATAATGTGGCCTCA | 254065 |
rs772029094 | snp | A/T | 4.9016e-05 | 0.00495031 | intron-variant | BRWD3 | GRCh38.p7 | X:80809402 | GCGCTAAGCCCCCAT[A/T]CCCTTAGCACCCCCC | 254065 |
rs772031266 | snp | C/T | 2.33932e-05 | 0.00341995 | intron-variant | BRWD3 | GRCh38.p7 | X:80733418 | GGTAGTAAAATATAT[C/T]AAACATTTGTTTACA | 254065 |
rs772043428 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781034 | AGCTTAGAGCAACAC[A/G]TAAATATTAATTTGG | 254065 |
rs772051921 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80713041 | CAGCCCCCCGCCCGG[C/T]CAGCTGCCCCGTCTG | 254065 |
rs772068794 | in-del | -/AT | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80726120 | ATGTGTCTGTATAAC[-/AT]ATAACACGTTTACAT | 254065 |
rs772082084 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771771 | CAAACAAATTTACAA[C/G]AGAAAAACAAACAAC | 254065 |
rs772090599 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767469 | CAGCTGAGGACCTAA[A/C]TGTTAGAAGGAAAAC | 254065 |
rs772093058 | snp | A/G | 5.53963e-05 | 0.00526261 | intron-variant | BRWD3 | GRCh38.p7 | X:80696011 | CAGAAAATAAAGCAC[A/G]TATGAATCAATATAG | 254065 |
rs772111533 | snp | A/G | 2.28788e-05 | 0.00338214 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722764 | AGGACGATAATCCGT[A/G]TGGAAGAACATCTGA | 254065 |
rs772113153 | snp | C/T | 1.65433e-05 | 0.002876 | intron-variant | BRWD3 | GRCh38.p7 | X:80699924 | ATTCCAAAGCTACTT[C/T]CATTGCATAGCTTAT | 254065 |
rs772128420 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769680 | ACACCACAATTAAAA[A/G]AACTAGAGAAGCCAA | 254065 |
rs772136596 | snp | C/T | 2.76786e-05 | 0.00372002 | intron-variant | BRWD3 | GRCh38.p7 | X:80684213 | CAATATTAAGGAATA[C/T]AATGGGACTAAAATT | 254065 |
rs772145800 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749842 | CCTGATTTTAAAATG[C/T]ATGATAAAGCTTATT | 254065 |
rs772147378 | snp | A/C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768300 | CCCCAAGGTTGAAAG[A/C/G]AAGGAAAAAATGTTA | 254065 |
rs772168029 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80771042 | TAGGAATCCAACTTA[C/T]AAGGGATGTGAAGGA | 254065 |
rs772169738 | in-del | -/TTGG | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80746088 | AGAATAAAACTGTAC[-/TTGG]TTAAGTATATTCCTC | 254065 |
rs772170179 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80781543 | GTTGGGGAGGTTGGC[C/T]GATGACTGCTCTAAC | 254065 |
rs772173291 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80686138 | GATGAAGCTGGAAAC[C/T]ATCATTCTCAGCAAA | 254065 |
rs772192859 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788071 | CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 254065 |
rs772201223 | snp | A/G | 2.59077e-05 | 0.00359906 | intron-variant | BRWD3 | GRCh38.p7 | X:80722515 | GAACAGCAGTAATGT[A/G]TAACATTGGGCAAAA | 254065 |
rs772205298 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684568 | CATATTTCCACGATT[C/T]CTTGCTATGAGAACA | 254065 |
rs772211667 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800302 | ACAGTGGCTTAGGTC[C/T]GTAATCCTAGGAGGA | 254065 |
rs772214465 | in-del | -/ATGT | 0.00105904 | 0.0229869 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669242 | AAACGGAAAGCAAAA[-/ATGT]ATGTACCACAACCTT | 254065 |
rs772227764 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779193 | GGTGGCGCATGCCTG[A/C]AATCCCAGCTACTCA | 254065 |
rs772236074 | snp | A/G | 8.02182e-05 | 0.00633267 | intron-variant | BRWD3 | GRCh38.p7 | X:80703452 | TCTTGAGGCTCCACA[A/G]AAAAAGGTTATAACA | 254065 |
rs772240639 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778826 | CAACATGGTGACACC[C/T]TGTCTCTACTAAAAA | 254065 |
rs772243975 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738493 | TGGGAGAATAATATA[C/T]CACTGATGTTAATAA | 254065 |
rs772251258 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80756125 | CTTCTCCCAGTTCAG[C/T]GGTTTATTTATTTAT | 254065 |
rs772269698 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777208 | ACGACAGAATTTTAC[C/T]CCCAAGAAAGATGAG | 254065 |
rs772273224 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701458 | GAGACTGAGGCAGGA[A/G]GATCGCTTTGAACCC | 254065 |
rs772275659 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674637 | TGAATCTCTACTATG[G/T]TTTAAAGTGGCAGCT | 254065 |
rs772280598 | snp | C/T | 2.28438e-05 | 0.00337955 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681394 | GCTTTCCCTGGGTCA[C/T]GGCTATTTCCACTTC | 254065 |
rs772290970 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697023 | TGGCTCTTAACTCCT[A/G]ATAGCAGGTTGTAGT | 254065 |
rs772298068 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792476 | TTTTTTTCTCTTTCA[C/T]GTTTAAGTCAAAAAA | 254065 |
rs772313894 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80778400 | AATATGGAGGTGCAG[C/T]GGGGGATGAAGCAAG | 254065 |
rs772347303 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685399 | TATAAGATTCATGTA[C/T]AGTATGGAGAGTTTA | 254065 |
rs772351163 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675698 | AAGAGGTAGCTGAGC[C/T]ACTGTTCAAAGAAGT | 254065 |
rs772370255 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715392 | GCAAATTCAGGGTCC[A/G]TTACCTAGATTTGTT | 254065 |
rs772373825 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707600 | TAGCATTTTTTTGAA[A/T]TCTGCCCTCAAAAAA | 254065 |
rs772376384 | snp | C/T | 2.58558e-05 | 0.00359545 | intron-variant | BRWD3 | GRCh38.p7 | X:80707517 | TCCTACAACAAAGAG[C/T]CAGCAATTAAGATAT | 254065 |
rs772389940 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80711802 | ACCTCCTCCGTCACA[A/C]CCCCATGAGTTGTCC | 254065 |
rs772391793 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80803828 | ATCATTCTGCTATTC[G/T]AATTGACAATTTAAG | 254065 |
rs772391993 | in-del | -/AAGA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720625 | GTTAATTTGTTACTG[-/AAGA]AAGAAAAATATTGTT | 254065 |
rs772401163 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770884 | AAATCTCCTGAAGCT[C/G]ATAAGCAACTTCAGC | 254065 |
rs772410263 | snp | C/T | 5.39418e-05 | 0.00519307 | intron-variant | BRWD3 | GRCh38.p7 | X:80809232 | CGACTCCCAGATCTC[C/T]TTCTTCCCCTTACCT | 254065 |
rs772425479 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730655 | TATACTAAAAACCAA[A/T]GAATTTTATGTCATG | 254065 |
rs772439854 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739145 | AAAACAGGACAGCAA[-/T]AACAGAGGTCATGAG | 254065 |
rs772448434 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784946 | TTCTGGTTCTAGAAC[A/C]TTGAGGAATCATCAC | 254065 |
rs772459773 | in-del | -/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80762566 | AAAAGGGTATGTGTT[-/G]GGGGGGTGGGGAAAG | 254065 |
rs772486706 | snp | A/G | 5.42138e-05 | 0.00520614 | intron-variant | BRWD3 | GRCh38.p7 | X:80736122 | TGATTCAAATAAAAA[A/G]TTTTCATGTTCAGCC | 254065 |
rs772508096 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | BRWD3 | GRCh38.p7 | X:80712301 | TTGCAGGCACGCGCC[A/G]CCACACCTGACTGGT | 254065 |
rs772514067 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793000 | AACCCTGTCTGTACT[A/G]AAAATACAAAAATTA | 254065 |
rs772527943 | snp | C/T | 1.73522e-05 | 0.00294547 | intron-variant | BRWD3 | GRCh38.p7 | X:80745772 | ACTTAAAAGTGAAAC[C/T]GATTTCATGAAATTA | 254065 |
rs772532209 | snp | A/C | 7.06356e-05 | 0.00594246 | intron-variant | BRWD3 | GRCh38.p7 | X:80691012 | AAAGCAAAAGCCATA[A/C]AGCTATAAATTTTAT | 254065 |
rs772543556 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809595 | TCCGCCGCACTCCTC[A/G]TCCTAGTTTCGCTCT | 254065 |
rs772547992 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784791 | CTGCCTATCATTGAT[A/G]GGCATTTGGGTTGGT | 254065 |
rs772553110 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770229 | CAATAGAAAAAGAGG[A/G]AAACCTCCCCAACTC | 254065 |
rs772556700 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80723142 | GCTTATTTTTATTCA[A/G]ATGAAGATAGATGAA | 254065 |
rs772569927 | snp | G/T | 2.28344e-05 | 0.00337886 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744128 | CTTATCACAGCTGCC[G/T]GCAGCAATAAGAGTG | 254065 |
rs772572745 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80692828 | TTACAGGTACAGGTA[C/T]TGTGAGACTAGATAA | 254065 |
rs772579851 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764044 | TGGAACAGAATAAAG[A/G]GCCAAAAAAATTTGC | 254065 |
rs772583017 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800042 | GTGCCCAGAGGTCAG[C/T]AGAGAACTAAGGAAG | 254065 |
rs772601305 | snp | A/C | 4.86429e-05 | 0.00493144 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707474 | AGGATCCTCTACCGA[A/C]GCGTCACTTGTGCCA | 254065 |
rs772612792 | snp | A/G | 4.34764e-05 | 0.00466222 | intron-variant | BRWD3 | GRCh38.p7 | X:80692014 | AAAAAATTAGAAAAA[A/G]TTATTTTCCAATATC | 254065 |
rs772617067 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731723 | CACGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 254065 |
rs772639231 | in-del | -/AATAT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784069 | TTTTAAATAACTAAA[-/AATAT]AATTGGAATGTCTGT | 254065 |
rs772640232 | snp | C/T | 2.43905e-05 | 0.00349209 | intron-variant | BRWD3 | GRCh38.p7 | X:80692193 | AAATTAATCATATAG[C/T]ACTTCCTTTCATATA | 254065 |
rs772655042 | snp | A/G | 7.12242e-05 | 0.00596716 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691166 | AACAGCAAAAGGGCT[A/G]GCAAAATCTACAAAA | 254065 |
rs772657050 | snp | C/G | 2.40162e-05 | 0.00346519 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677322 | TTCCTGTCCGGGGCT[C/G]TCTGCCATCACCATT | 254065 |
rs772658907 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752826 | CCCGCCACCACACCC[A/C]GCTAATTTTTGTATT | 254065 |
rs772661095 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80741017 | TGCACCCATTAACTC[A/T]TCATTTAACATTAGG | 254065 |
rs772685224 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80728001 | ACAGCATTTGCAAAA[C/T]AGAAGAACTTTACAT | 254065 |
rs772686412 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724568 | ATTACTAAATCATAT[A/G]AGGTTTACCAGAGGC | 254065 |
rs772702889 | snp | A/T | 5.24583e-05 | 0.00512117 | intron-variant | BRWD3 | GRCh38.p7 | X:80682679 | TTATATTTTAAAAAA[A/T]GGTATAAACATGCCT | 254065 |
rs772707529 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807579 | CCTTTCTCCTTTCAC[C/T]ACCCTCCAATGCACT | 254065 |
rs772708059 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794271 | AGCACTTTTAGAGGC[C/T]GAGGCAGGTGGATGG | 254065 |
rs772714229 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80745135 | ACCAAAAAAAAGATA[C/T]AAAAAATAGCTATAA | 254065 |
rs772714389 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721907 | TCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 254065 |
rs772717881 | in-del | -/AGTT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775166 | TTTTCACAGCAACAG[-/AGTT]AGTTGAGTAATTGCA | 254065 |
rs772749962 | snp | C/T | 2.28532e-05 | 0.00338025 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682042 | CATGAGATACTGAGG[C/T]ATTCTGGTCATTTTT | 254065 |
rs772763988 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80708533 | TAAGAACTGTGAATG[C/G]GGCCAGGTGCAGTGG | 254065 |
rs772780488 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798759 | CAACATAGTGAGACC[G/T]CCATCTCTACCAAAA | 254065 |
rs772796194 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766761 | TCTTTGGCACTGGTT[A/G]GACAGTGGGTGCAGC | 254065 |
rs772808028 | snp | A/G | 2.31107e-05 | 0.00339924 | intron-variant | BRWD3 | GRCh38.p7 | X:80724900 | AGAGAAGTTGGTTTT[A/G]ATGTGAACTAGATAC | 254065 |
rs772827290 | in-del | -/AAAAAAAACAGACCTGT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80691039 | TATAATAAGTGATTA[-/AAAAAAAACAGACCTGT]AAAAAAAACAGACCT | 254065 |
rs772836252 | snp | A/G | 2.34618e-05 | 0.00342496 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709546 | CGCTGTGTCCTGCGT[A/G]AAGAACGCCCACAGC | 254065 |
rs772846177 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759024 | TAGTTTATCAATGTC[A/T]GAGCCTTTTAAAATA | 254065 |
rs772860021 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80720880 | ATATACAAATATGTA[C/T]CATTGTATGTATAAC | 254065 |
rs772860615 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671274 | ATTTAAAGTGTAAAC[A/T]TCATATTTATTATCC | 254065 |
rs772864666 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80758156 | GTGAGCCAAGATCGC[A/G]CCATTGCACTCCAGT | 254065 |
rs772874852 | snp | A/G | 2.28198e-05 | 0.00337778 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682468 | ATGTAATGATACCTA[A/G]GTGCTCCACTACTAG | 254065 |
rs772881588 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678162 | CCAGTTGGGCATCCA[C/T]TGCAGTATTCTAGGT | 254065 |
rs772881729 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80676538 | ACACAACTTGCTTTG[C/T]AGATTTCCTGGTAAA | 254065 |
rs772886292 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782954 | GCTCAAACAACTCAA[C/T]AGAAAAAAAAAATCT | 254065 |
rs772889567 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804952 | AAATTTAGAGTGTTA[G/T]ATTTTAAATGCCATA | 254065 |
rs772900532 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735592 | TGGGAAGGACAAGGT[C/T]AGGAGATCGAGACCA | 254065 |
rs772906692 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728453 | ACGGTAACAATGAAA[A/T]AATGCCAACCCCTGC | 254065 |
rs772912530 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715742 | CATAAATAAGTGAAC[A/G]TGGCTGTGTTCCAAT | 254065 |
rs772917937 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740418 | CACTATGTGGACAAT[C/T]ATTAAAAGAAGCCAA | 254065 |
rs772944369 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80721703 | CTATCTTCCTATCAT[A/G]TATCACATTCATCTC | 254065 |
rs772947470 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798156 | AACACTAGAGAAACA[A/G]ATTTGATCAAAATAA | 254065 |
rs772951086 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80727241 | TCTGCAGTCACTCTT[A/G]GCCCATTCCAATCTA | 254065 |
rs772965771 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713044 | CCCCCCGCCCGGCCA[A/G]CTGCCCCGTCTGGGA | 254065 |
rs772991514 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764503 | TATTTTTAGTATAGA[C/T]GGTGTTTCACCATGT | 254065 |
rs773037538 | in-del | -/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80698281 | ATCTTCATAGGTATA[-/G]GGTCCTGCTTAAAGT | 254065 |
rs773038939 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80722493 | CAGGAGGCATACATC[A/C]TAGAGAGAACAGCAG | 254065 |
rs773041756 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779623 | TTTGGTGAAGCTTCG[C/T]TGGGGGTTTCCTAAA | 254065 |
rs773053188 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80805905 | CCGCCACTGCACTCC[A/C]GCCTGGCAATAGAGC | 254065 |
rs773076871 | in-del | -/CTAA | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80781554 | TGGCCGATGACTGCT[-/CTAA]CTGCTTCCTGCTGAA | 254065 |
rs773085572 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706070 | TTTGACTTTTTTGTA[A/C]TAACACTTAGCTTAA | 254065 |
rs773099854 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769123 | TACAAAGAGACTTAC[A/G]CTCCCATGCAATAAG | 254065 |
rs773108873 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796235 | TCCTGGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 254065 |
rs773141773 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688198 | TTAGATGGACATTTA[C/G]AAATAAACGGGAAAT | 254065 |
rs773158130 | in-del | -/AT | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80699424 | TATGTGCATGTGTGC[-/AT]ATATATATATACACA | 254065 |
rs773192006 | snp | C/T | 3.33923e-05 | 0.00408596 | intron-variant | BRWD3 | GRCh38.p7 | X:80692029 | ATTATTTTCCAATAT[C/T]ATGTGATTACCATTT | 254065 |
rs773214431 | snp | C/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669230 | AATTTTTGAAAAAAA[C/T]GGAAAGCAAAAATGT | 254065 |
rs773220635 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80678751 | AGACTGGAAGAATTG[A/C]AAAGAAGACTAGGGC | 254065 |
rs773232550 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80726310 | ACGTTTACATGTTAT[A/G]TCTGTATAACATATA | 254065 |
rs773237783 | snp | A/C | 4.33304e-05 | 0.00465439 | intron-variant | BRWD3 | GRCh38.p7 | X:80699935 | ACTTCCATTGCATAG[A/C]TTATGAATTTGGCAA | 254065 |
rs773238659 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707739 | ACATCTTTTTGTGAT[A/T]TCAAAGACTCAATAG | 254065 |
rs773243563 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684717 | AGGTCCATAATTCAT[C/T]TGATTTTGATTAGGG | 254065 |
rs773259793 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80763891 | TCTAAAATTCACAGG[A/G]AAAGACCCTAGAATA | 254065 |
rs773265280 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750013 | AGTTTCTTCAATAAG[C/T]GGTGCTGGGAAACTG | 254065 |
rs773300485 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761000 | TGCAGTGAACTATGA[C/T]CTTGTCAGTGAACTC | 254065 |
rs773306966 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80777346 | GTTTATCATCAAATT[A/G]GCACCAAGTTCAGAT | 254065 |
rs773344862 | in-del | -/AAAG | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771829 | AACAGACACTTCTCA[-/AAAG]AAGACATTTATGCAG | 254065 |
rs773357513 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740014 | CCAGAAATAATCAGT[C/T]AGATATGATAGTGAG | 254065 |
rs773363074 | in-del | -/CCGCACCAT | 2.31798e-05 | 0.00340432 | cds-indel, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723852 | ATTTACAATCAAACA[-/CCGCACCAT]GGCCTTGGCCTTCAA | 254065 |
rs773376384 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80741064 | ATCCATCCCCCCTCC[C/G]CCACCCCACAACAGG | 254065 |
rs773396901 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80787702 | TCTCTGTGAGCATGA[A/G]TTAGGCAAAGATTTA | 254065 |
rs773400385 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80762567 | AAAGGGTATGTGTTG[C/G]GGGGGTGGGGAAAGG | 254065 |
rs773404090 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719828 | ATGTACTAGCTTATG[C/T]GTCTGACTTAACCAA | 254065 |
rs773407704 | snp | C/T | 2.29274e-05 | 0.00338573 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686902 | CTGTCGAAATGGCTC[C/T]GAGTCTTCACGTTCA | 254065 |
rs773414044 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80778849 | ACTAAAAACACAAAA[A/C]TTAGCTGAGCGTGGT | 254065 |
rs773420746 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802623 | ACAGCATTTTACAAT[A/T]AACAAAATGCATTCT | 254065 |
rs773424146 | snp | G/T | 7.51202e-05 | 0.00612817 | intron-variant | BRWD3 | GRCh38.p7 | X:80703458 | GGCTCCACAGAAAAA[G/T]GTTATAACAGGTAAT | 254065 |
rs773479410 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681748 | TGCTCTGAGATATTA[C/T]AGGCATCATTTAATC | 254065 |
rs773483394 | in-del | -/AA | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80769727 | AAGTTAGCAGAAGGC[-/AA]GAAATAACTAAGATC | 254065 |
rs773490269 | in-del | -/T | 0.0132835 | 0.0804072 | intron-variant | BRWD3 | GRCh38.p7 | X:80719060 | CTTGTCTTCAGTGTA[-/T]TTTTTTTTTTTTATT | 254065 |
rs773499002 | snp | C/T | 2.96244e-05 | 0.00384855 | intron-variant | BRWD3 | GRCh38.p7 | X:80685420 | GGAGAGTTTAGAAAG[C/T]AAAAACAATCAATAT | 254065 |
rs773509271 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80747000 | GATGCTGAGTAAATA[A/T]TGGGAGGAACTGCAT | 254065 |
rs773534059 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80686173 | CTCAAGGACAAAAAA[A/C]CAAACACCGCATGTT | 254065 |
rs773544979 | snp | C/T | 4.66619e-05 | 0.00482999 | intron-variant | BRWD3 | GRCh38.p7 | X:80733426 | AATATATCAAACATT[C/T]GTTTACACAAATATG | 254065 |
rs773556295 | snp | A/T | 3.3915e-05 | 0.00411781 | intron-variant | BRWD3 | GRCh38.p7 | X:80736124 | ATTCAAATAAAAAGT[A/T]TTCATGTTCAGCCTA | 254065 |
rs773557937 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790426 | GTACCAGTTACTACA[C/T]GAAAATACATCATGA | 254065 |
rs773569356 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754345 | CTACTAATTTTTGTA[C/T]TTTGATTTTGTAACC | 254065 |
rs773616661 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792083 | ACCAAAATGAAAATA[A/G]TAGGCATATATTTGA | 254065 |
rs773626233 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80730656 | ATACTAAAAACCAAT[A/G]AATTTTATGTCATGT | 254065 |
rs773635146 | snp | C/T | 5.32467e-05 | 0.00515951 | intron-variant | BRWD3 | GRCh38.p7 | X:80809238 | CCAGATCTCTTTCTT[C/T]CCCTTACCTGAGCGG | 254065 |
rs773636366 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701463 | TGAGGCAGGAGGATC[A/G]CTTTGAACCCAGGAG | 254065 |
rs773645892 | snp | A/G | 2.28154e-05 | 0.00337745 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744179 | GTCAGAAATTTCAGC[A/G]GAGTGTCCACGAAGT | 254065 |
rs773657193 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809625 | TCTCTCGAATTCATC[G/T]CATCACGTTTCGACC | 254065 |
rs773664860 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675747 | ATTTTTCAAATGTTT[A/G]AGTTATTTAAGCTAC | 254065 |
rs773691063 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805663 | ACCCCAGGCCGGGCG[C/T]GGTGGCTCATGCCTG | 254065 |
rs773692825 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788862 | AGGCTACTTACTACC[-/T]GATTTAATTTAGATG | 254065 |
rs773723606 | snp | C/G | 0.00376309 | 0.0432132 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809458 | GCTTCGATCTGGGTA[C/G]GTGCTGCCGCCATCC | 254065 |
rs773734981 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680793 | TCATTTAGTTTTTTT[C/T]TCCCAATTCCTTTTA | 254065 |
rs773739794 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764987 | ATACAATATATGGTG[C/T]TATTTTTCCCACAGC | 254065 |
rs773760388 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714159 | ACCTATTTTCTCTGA[A/G]GTTTGCTACCTGGAG | 254065 |
rs773785838 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773334 | CTTTGTTTCTGCTAT[G/T]CCTTTAGCCTTATGC | 254065 |
rs773787701 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766118 | AAGCAGATTGCCCTC[C/T]CCAATGAATCCGGTG | 254065 |
rs773802570 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721908 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACC | 254065 |
rs773805416 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80735464 | TTCTTACCAAAGTAA[A/G]AAATGAAACAAATAA | 254065 |
rs773812415 | snp | G/T | 0.00011783 | 0.00767471 | intron-variant | BRWD3 | GRCh38.p7 | X:80691776 | AACTTCTGCTGATTT[G/T]CCTAGCTCTCTTGCA | 254065 |
rs773846435 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757283 | AATACACTTCTAAAA[A/G]CTCATTAAAACAGGG | 254065 |
rs773849488 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680679 | GCCACAAAAATATGA[A/G]ACCTATTTAAAGATG | 254065 |
rs773852448 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80718751 | AATGCAATGTTACAC[-/A]GATAAATGACTCTAG | 254065 |
rs773867970 | snp | C/G | 2.4166e-05 | 0.00347598 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677333 | GGCTCTCTGCCATCA[C/G]CATTTGTAAGGGGTC | 254065 |
rs773869847 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80690866 | TATTCCTCTCAGCCT[C/T]TCTTCTCTATCCCCA | 254065 |
rs773895387 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743072 | TGAGATACATCCCAT[C/G]AATACCTAATTTATT | 254065 |
rs773900038 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798053 | TGAGCCGAGATCACG[C/T]CACTGCACTCCAGAC | 254065 |
rs773923350 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697379 | TGTTACAGAGATATA[C/T]TGCATAATGGTGGGG | 254065 |
rs773927277 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80784949 | TGGTTCTAGAACCTT[C/G]AGGAATCATCACAGT | 254065 |
rs773944264 | snp | A/C | 2.681e-05 | 0.00366119 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745627 | ACAGATGACAAGTGC[A/C]CCAGAATTCTCTTAT | 254065 |
rs773950619 | snp | A/G | 2.33689e-05 | 0.00341817 | intron-variant | BRWD3 | GRCh38.p7 | X:80728957 | ATTTTTGACAAAGGT[A/G]CATGTTAAATAGCAA | 254065 |
rs773951921 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781501 | CTGTCTCTCAGTCCC[C/T]CCTCTCAACAAGAAA | 254065 |
rs773965798 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767136 | GCGGAGCCCACCTCA[G/T]CTCAGCAAGAAACTT | 254065 |
rs773972429 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714936 | GATTTAATTTTTAAT[A/G]ATTAAAATTTGAAGT | 254065 |
rs773974950 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80747484 | AGTATAAAAGCAAAA[A/C]ACATCATTACCAATA | 254065 |
rs773976229 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756725 | TTACTGGGAAGAACT[A/G]GATCTCATTCTTCTA | 254065 |
rs773982015 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732141 | AACATAAATGAACTG[A/T]GTTTAGACTTGGGTT | 254065 |
rs773992493 | snp | A/G | 2.28684e-05 | 0.00338137 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682015 | GAGATGAGAAAGGAG[A/G]GCTAGTCCTGGCATG | 254065 |
rs774008222 | snp | C/G | 2.2887e-05 | 0.00338274 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681452 | AAAATGGCCCATCTG[C/G]CTCATCATCAAGTAG | 254065 |
rs774008422 | snp | A/G | 2.65752e-05 | 0.00364512 | intron-variant | BRWD3 | GRCh38.p7 | X:80681529 | GATTTTAATACTAAC[A/G]TAATTATCATGTTTT | 254065 |
rs774010603 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782827 | GAAGCTCACTAGGAG[C/T]TCGTGGCTGCAGTGA | 254065 |
rs774015440 | snp | G/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673695 | GAATTTAAACATTAT[G/T]AGCATTTATGAGAAA | 254065 |
rs774030088 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80697350 | TTCAGATTCATGGGG[C/T]ACACGTGCAGGTTTG | 254065 |
rs774031730 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795494 | CTATACATGTATGTG[-/TA]TATATGTATATGTAT | 254065 |
rs774032240 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796004 | GAGAGAAGATATTTT[C/G]TGTGTTTTTTTTTCA | 254065 |
rs774033701 | snp | A/G | 4.689e-05 | 0.00484178 | intron-variant | BRWD3 | GRCh38.p7 | X:80745745 | CTGAAAAAAATACGA[A/G]ATTAACTTAAAACTT | 254065 |
rs774034895 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734435 | CACTGAATACAGGCC[A/G]CCTATGATCATAAAC | 254065 |
rs774051062 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766821 | GCACTGCCTCACGCC[A/G]GAAGTGCAAGGGGTC | 254065 |
rs774058638 | snp | C/T | 3.30316e-05 | 0.00406383 | intron-variant | BRWD3 | GRCh38.p7 | X:80684198 | TTAAATACTGTATAG[C/T]AATATTAAGGAATAC | 254065 |
rs774068057 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714043 | TAGCCCTGCAAAGTT[G/T]TCTCTTGTGGGGGAA | 254065 |
rs774072328 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734859 | GCAGTAAACTTTTTT[-/G]TTAGTGGGTATTTAG | 254065 |
rs774091259 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688279 | GAGGGAGACTCACAC[A/C]AAACTTTCCCAATAT | 254065 |
rs774106073 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720864 | GTCTAGATATGCTTA[C/G]ATATACAAATATGTA | 254065 |
rs774117692 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725918 | CATATGTTACATGCC[-/TA]TATGACATAACTTGT | 254065 |
rs774134615 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770981 | ACAGAGAGCCAAATC[A/C]TGAGTGAACTCCCAT | 254065 |
rs774185965 | in-del | -/CCA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727156 | AGCACACTTTTATTT[-/CCA]CCACCACCACACAAA | 254065 |
rs774186344 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788310 | GGAGACAACTGCACA[G/T]TGAGAGAAAATATTT | 254065 |
rs774191113 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80698122 | TCTTTTAAGAAGTGT[C/G]TGTTCATGTCCTTTG | 254065 |
rs774221300 | snp | A/G | 5.65355e-05 | 0.00531644 | intron-variant | BRWD3 | GRCh38.p7 | X:80809203 | CTCGATTTCCCCACT[A/G]GGACCATTCACCACG | 254065 |
rs774222568 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779505 | AGCAAAGCAGATCGC[C/T]TGAGGTCAGAAGTTC | 254065 |
rs774237023 | in-del | -/CTGTTGCC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764340 | AGACGGAGTCTCGCT[-/CTGTTGCC]CAGGCTAGAGTGCAG | 254065 |
rs774238873 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776442 | CATTCAGGAAAGTCC[G/T]TAAGTAAAATTAATA | 254065 |
rs774248620 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80754930 | AGAGAATCTCTTGAA[C/T]CCAGAAGGCGGAGGT | 254065 |
rs774280684 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715564 | ACAGATCATATTTTG[C/T]TCCTAAATGATTTGG | 254065 |
rs774298874 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712562 | TTGCAGCCTCTGCCC[A/G]GCCGCCACCCTGTCT | 254065 |
rs774310965 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762991 | AAGGAATAGTGATCG[C/G]TACTATAAAGAAAAT | 254065 |
rs774311493 | in-del | -/T | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80789385 | TAAATTTTTTTTTTC[-/T]TTTTTTTTGAGACGG | 254065 |
rs774323609 | snp | C/T | 2.32385e-05 | 0.00340862 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709536 | CTGACGTTTGCGCTG[C/T]GTCCTGCGTAAAGAA | 254065 |
rs774356139 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748267 | ATCTGCCCACCTCGG[A/C]CTCCCAAAGTGCTGG | 254065 |
rs774356930 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733870 | ATAAATCAATCATTT[C/G]CTGTTTCCCACATCA | 254065 |
rs774357935 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80787183 | AAGACCTGAACACTG[-/A]AAAACTACAAAACGC | 254065 |
rs774365997 | snp | C/G | 2.46975e-05 | 0.00351399 | intron-variant | BRWD3 | GRCh38.p7 | X:80719449 | AGTAAAATAATTACA[C/G]TACATAAACTACACC | 254065 |
rs774379848 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726873 | GTTATAACAAAATCC[C/T]TTGCTAAAAGAATCA | 254065 |
rs774396996 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748091 | CAGATGATTCGCCCA[C/T]CTCAGCCTCCCAAAG | 254065 |
rs774401384 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770506 | AGACAAAAACCACAT[A/G]ATTATCTCAATAGAT | 254065 |
rs774404451 | in-del | -/ATATA/TA | 0.396587 | 0.202944 | intron-variant | BRWD3 | GRCh38.p7 | X:80786516 | CCCTTTTAATTTGCC[-/ATATA/TA]TATATATATATATAT | 254065 |
rs774405109 | snp | A/T | 3.36513e-05 | 0.00410177 | intron-variant | BRWD3 | GRCh38.p7 | X:80730060 | TTAATTTTCTCAAAA[A/T]TGTAAATCACTTTTT | 254065 |
rs774407098 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80692414 | AGAGAATAAACATTT[C/T]GTCTATCATTCTTGA | 254065 |
rs774424471 | snp | A/C | 4.75998e-05 | 0.00487828 | intron-variant | BRWD3 | GRCh38.p7 | X:80699916 | GCAATTTAATTCCAA[A/C]GCTACTTCCATTGCA | 254065 |
rs774426044 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740071 | ATCAAAATGCATGAA[A/G]TAATTTCAAATAATC | 254065 |
rs774427130 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80705190 | AGAATCACTTGAATC[C/T]AAGAGGCAGAGGTTG | 254065 |
rs774432879 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775201 | AGACCAAATGTTCCA[C/G]AAAGCCAAAAACATT | 254065 |
rs774454877 | in-del | -/A | 0.000157573 | 0.00887479 | intron-variant | BRWD3 | GRCh38.p7 | X:80745732 | AGGTGATATTCACTG[-/A]AAAAAAATACGAAAT | 254065 |
rs774462148 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684529 | TCACATATGATTAAA[C/T]TGTTCCACTCTACAA | 254065 |
rs774479181 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767350 | GGGACAAAGCTTCTA[A/G]AAGAAGTATCAGGCA | 254065 |
rs774497770 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780897 | TTAGACTACTTTCTT[C/T]CCATTTACATTTACA | 254065 |
rs774502311 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702813 | TTGCAATGACAATAT[C/T]ACATTTCTACTAACA | 254065 |
rs774540015 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80769624 | TTACAGCACTAAATG[C/T]CCCTAACAGAAAGCA | 254065 |
rs774541526 | snp | C/T | 7.18546e-05 | 0.00599351 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677315 | CTCTTGATTCCTGTC[C/T]GGGGCTCTCTGCCAT | 254065 |
rs774544522 | in-del | -/TG | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726112 | TACATGTTATGTGTC[-/TG]TATAACATATAACAC | 254065 |
rs774551178 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80737601 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 254065 |
rs774563437 | snp | A/G | 2.28621e-05 | 0.00338091 | intron-variant | BRWD3 | GRCh38.p7 | X:80719683 | CAGATACAAAGCCAC[A/G]AAATTACTTACATTT | 254065 |
rs774567676 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745260 | AACAAACATTTAATA[A/C]ATGTTTGTTAAAACT | 254065 |
rs774577216 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80760743 | TGTGATTCTTTTCTT[A/T]CTTTCTTTCTTCATT | 254065 |
rs774590527 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696525 | AACATAAATACACAC[-/AC]ACACACACACACACA | 254065 |
rs774613445 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768990 | AAGATCAAAAGAAAC[A/G]AAGAAGGACATTACA | 254065 |
rs774622951 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705875 | GTTGCCGTGGGTGAG[C/T]CAGTGAGTGATGGTG | 254065 |
rs774623401 | snp | C/T | 2.34357e-05 | 0.00342305 | intron-variant | BRWD3 | GRCh38.p7 | X:80683964 | CCAATTTTCAGTAAC[C/T]GGTTAAAGAAAACTG | 254065 |
rs774634790 | in-del | -/ATAAC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725989 | ATGTTATATGTCTAT[-/ATAAC]ATAACATGTTTACAT | 254065 |
rs774639694 | snp | A/T | 2.76947e-05 | 0.0037211 | intron-variant | BRWD3 | GRCh38.p7 | X:80696013 | GAAAATAAAGCACAT[A/T]TGAATCAATATAGAG | 254065 |
rs774653389 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80787425 | AATTTTTTGAAAATG[A/C]GAGCAAAGTTGGAAG | 254065 |
rs774680562 | in-del | -/CTTT | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80695826 | CTAAATGATAAGCTA[-/CTTT]CTTTCTGTTAAATCA | 254065 |
rs774684358 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700475 | GGCATGGTGGCTCAC[A/G]CCTTTAATCCCAGCA | 254065 |
rs774702727 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769161 | GACTTTAACACCCCA[C/T]TGTCAACATTAGACA | 254065 |
rs774704797 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790148 | CAGAGATTGTGCCGA[C/T]GCACTCTAGCCTGAG | 254065 |
rs774748578 | snp | C/G | 0 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80729997 | CTTGCCGTTCCATCT[C/G]GACTTCCACTAACAA | 254065 |
rs774760992 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782950 | AGGAGCTCAAACAAC[A/T]CAATAGAAAAAAAAA | 254065 |
rs774763415 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758914 | ACATTACTCACAGCT[A/G]TAATTTATAGATACT | 254065 |
rs774765394 | in-del | -/AT | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80801099 | GATAAAATAAACCAA[-/AT]ATATATATATCTATA | 254065 |
rs774783559 | in-del | -/CTTTT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680803 | TTTTTCTCCCAATTC[-/CTTTT]ATTTTATTTATTTAT | 254065 |
rs774800609 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80681285 | GCTTTTAAATGATTT[A/G]TCTGCTATCATAAAG | 254065 |
rs774801294 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721789 | CCCTACACCCAATAA[C/T]TCTTTGCATTTCAAA | 254065 |
rs774805395 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685297 | GAGAACACATGTTGA[C/T]TCAGAAAGAGGAACA | 254065 |
rs774811293 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791055 | GATTTTGTCTAAATA[G/T]ATCTTAAGAAATATT | 254065 |
rs774818867 | snp | C/G | 4.81464e-05 | 0.00490621 | intron-variant | BRWD3 | GRCh38.p7 | X:80704889 | CTAAGTATAGAAAAG[C/G]AGTAGTTTTACTTAA | 254065 |
rs774825723 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729035 | ATCCTAAACTATACC[A/G]TTAAGTATTCATGAA | 254065 |
rs774847109 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674570 | CAAGAGATAAATAAC[C/T]GAAACAGCACATTTT | 254065 |
rs774866489 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80730626 | CTGTGGTGATGGTTG[C/T]ACAACCCTATGAATA | 254065 |
rs774879639 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779442 | GCCAAAAACACTGGA[A/G]AGTGGCCAGGTGGAG | 254065 |
rs774883715 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731371 | GTTAAAAATTTAGGT[C/T]CTTCCATCATGAAAG | 254065 |
rs774888335 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802572 | CTATTCGGTCTCTCT[A/C]TCCTAATTTTAAAAT | 254065 |
rs774913067 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782734 | TGAGACCCTATCTCT[A/T]CAAAAATATATATAT | 254065 |
rs774971177 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80765914 | TATTTATTTATTTAA[G/T]TATTAAATACTTATT | 254065 |
rs774984085 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751929 | GGCTGAATAGTACTT[-/G]ATTATGTATATATAG | 254065 |
rs774987058 | in-del | -/ATC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771735 | TGACAAAGGGCTAAT[-/ATC]CAGAATCAACAAAGA | 254065 |
rs774987984 | snp | G/T | 5.48291e-05 | 0.0052356 | intron-variant | BRWD3 | GRCh38.p7 | X:80677405 | AGTTAAGCTTTGACA[G/T]TGACAAAATGGTTAT | 254065 |
rs774993546 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80771948 | AGTTAGAATGGCGAT[A/C]ATTAATAAGTCAGGA | 254065 |
rs775000945 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80781877 | ACAAAAAAAGGAAAG[A/C]TATTCCATATTCATG | 254065 |
rs775005246 | in-del | -/TGAAA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791629 | CTGCTAAGAAAGAAG[-/TGAAA]TGAAATGAAATAAAG | 254065 |
rs775021785 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80750920 | TAAGTCTTATAAAGG[A/G]AAGAAATTGGAAATT | 254065 |
rs775045207 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754211 | TGTTCTGTAGTTTTC[C/T]ATGTAGAGATCTTTC | 254065 |
rs775053370 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80690705 | AAATCTAATTAACTC[-/T]TGACCAAATTCTCCA | 254065 |
rs775061527 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80772439 | CACCTGGACACAGGG[C/T]GGGGAACATCACACC | 254065 |
rs775088571 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725957 | TTACATGTCTATATA[-/AC]ACATAACATGTTTAC | 254065 |
rs775090282 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805444 | TTGATATCCTAGTTA[-/AC]ACACTTCATTGTACA | 254065 |
rs775094050 | snp | C/T | 2.28527e-05 | 0.00338021 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80793635 | ACCTTTGGCATCCCG[C/T]AGCAGAGACTGCCGA | 254065 |
rs775100640 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801093 | ACTAGCAGATAAAAT[A/G]AACCAAATATATATA | 254065 |
rs775106759 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723565 | CTATTGTGATCTGCA[C/T]AGCCAAACCTAAGGT | 254065 |
rs775110803 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713562 | ACACTGCGGAAGGCC[G/T]CAGGGTCCTCTGCCT | 254065 |
rs775117514 | snp | C/T | 0.00041347 | 0.0143723 | intron-variant | BRWD3 | GRCh38.p7 | X:80734098 | CAAAAATAAAGCAAC[C/T]GTTTCTGATTTTCTC | 254065 |
rs775125852 | snp | C/T | 2.3079e-05 | 0.0033969 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709522 | GTTTGGTAAGTATGC[C/T]GACGTTTGCGCTGTG | 254065 |
rs775134822 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80696170 | GGGAGTGCCCTGCCT[A/G]CTGCCATATTACTTT | 254065 |
rs775137615 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807660 | CCTGTTTTTGTGTGT[C/G]AATGCTGAACACAAG | 254065 |
rs775144786 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697058 | TGCAAGGCTCTAAAC[C/G]AAGGATGAGCAGCCA | 254065 |
rs775179894 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766203 | GATTCCCTCTCTCTG[C/T]CTATTTTCAAGCTGA | 254065 |
rs775193820 | snp | A/G | 4.90034e-05 | 0.00494968 | intron-variant | BRWD3 | GRCh38.p7 | X:80691189 | CTACAAAATTATGAA[A/G]ATCAAATAAGGTAGC | 254065 |
rs775195900 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80752620 | GGTAAGATATTTCAT[C/T]GTGGTTTTAATTTAA | 254065 |
rs775196558 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722895 | AGAGAATCTTTTGCA[A/T]ACTCTTCTAGTCCTT | 254065 |
rs775264238 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80779358 | ATGCAATCCTCTGAT[C/T]GGTTAAAGTGTAGTA | 254065 |
rs775293773 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746217 | AAGTAAAAAAAAACT[A/G]TACAGTGAAAAGATA | 254065 |
rs775294346 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80788254 | CTGGGCAACAAAGCT[A/G]GACCCCATCTCAATT | 254065 |
rs775304535 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766770 | CTGGTTGGACAGTGG[A/G]TGCAGCCCTCGGAGG | 254065 |
rs775323578 | in-del | -/AA | 0.000613152 | 0.0174986 | intron-variant | BRWD3 | GRCh38.p7 | X:80691992 | AGCTAGGTATAAGAT[-/AA]AAAAAAAAAAATTAG | 254065 |
rs775334440 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808652 | AATGATGAAGGAAAA[A/G]CCTCCGCTCCCCATC | 254065 |
rs775358440 | in-del | -/T | 0.00844089 | 0.0644143 | intron-variant | BRWD3 | GRCh38.p7 | X:80789052 | CTTAAAAAGACAGCC[-/T]TTTATGTCAATAATA | 254065 |
rs775372562 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785181 | ATATTAATTACATAT[G/T]CCTCAGAATTTCCTT | 254065 |
rs775373177 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80756296 | CACCTGAGGTCAGGA[C/G]TTCAAGACCAGCCTG | 254065 |
rs775381186 | snp | A/G | 2.28149e-05 | 0.00337741 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682511 | TGCTGCTTCTTAGAC[A/G]TTTTCTGTACCGTGG | 254065 |
rs775385929 | snp | A/C | 2.32258e-05 | 0.00340769 | intron-variant | BRWD3 | GRCh38.p7 | X:80728950 | CTTATAAATTTTTGA[A/C]AAAGGTGCATGTTAA | 254065 |
rs775394376 | in-del | -/A | 0.00476314 | 0.0485683 | intron-variant | BRWD3 | GRCh38.p7 | X:80706585 | TTTCCTGTTCAACGG[-/A]AGGTATTCAGAGACA | 254065 |
rs775395128 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763729 | GGTGAAGAAAAAAAA[C/T]CAAAGACCACAATAA | 254065 |
rs775404811 | in-del | -/A | 4.74896e-05 | 0.00487263 | intron-variant | BRWD3 | GRCh38.p7 | X:80717767 | TCTCAGAGCTAAAAC[-/A]AAAACAAGGAAAATT | 254065 |
rs775405777 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80688156 | AGAGTGGGAAAAGAC[A/G]TTAAGTTACATTCAA | 254065 |
rs775412048 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669322 | TAACCACATTTAGAA[C/T]AAAAATGAACACAAA | 254065 |
rs775433900 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712955 | CTCCTCCGCCCGGCA[-/C]CCACCCCGTCTGGGA | 254065 |
rs775441651 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80719946 | AACCACATATACGAC[A/G]GTAGTCTCATAAGAT | 254065 |
rs775447334 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685700 | GTCATTCTCCTTTGC[C/T]ATGAAAAACACAAGA | 254065 |
rs775459008 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80797923 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 254065 |
rs775492150 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795377 | CACACATGTGTATAT[A/G]TACACACATATATAC | 254065 |
rs775499789 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710374 | TCATCTGCTGACTAT[A/T]TTGACTACAGAGCTA | 254065 |
rs775537057 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678631 | GTAAAGAGAGACAAC[A/G]TGGCTGAAGACTGAG | 254065 |
rs775546123 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793005 | TGTCTGTACTAAAAA[C/T]ACAAAAATTAGCTGG | 254065 |
rs775552302 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | BRWD3 | GRCh38.p7 | X:80717783 | AAAACAAGGAAAATT[A/G]TCACTTTGTGAGCAA | 254065 |
rs775560181 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778550 | GTTCATAGATCAGGC[C/T]TCTTGTACCATACCT | 254065 |
rs775567338 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80747225 | GTCTCTTCATACTTT[A/G]CAGGTAGATGCAGGG | 254065 |
rs775568178 | snp | C/G | 3.29468e-05 | 0.00405861 | intron-variant | BRWD3 | GRCh38.p7 | X:80808630 | AAGAAAGGGGGAAGC[C/G]GAGGCAAATGATGAA | 254065 |
rs775569122 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80757203 | ACCCTAAAAGTTAAG[C/T]AACATTATCCCAGGC | 254065 |
rs775569301 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796063 | GTTGGGCATAAAGCA[-/G]GACTAAATAAATATT | 254065 |
rs775578171 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80805868 | TGAACCTGGGAGGCG[A/G]AGGTTGCAGTGAGCC | 254065 |
rs775579561 | snp | A/T | 1.65258e-05 | 0.00287448 | intron-variant | BRWD3 | GRCh38.p7 | X:80682673 | CTAGTTTTATATTTT[A/T]AAAAAAGGTATAAAC | 254065 |
rs775585391 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746319 | GGTTTCTGAATTTAG[A/G]GGCTCTCCCTGTAGT | 254065 |
rs775603563 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80725822 | TGTTACATGCCTATA[A/T]AACATAACATGTTTA | 254065 |
rs775615171 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80702218 | CTACATATTCATTGT[C/T]TGGTTTACATACATC | 254065 |
rs775631135 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747986 | TCAGACTTCCTGTGC[C/T]ACATTGAATATAAGT | 254065 |
rs775631250 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80723963 | TGTTAATACCATGGA[A/C]TCTGTGATACACAAA | 254065 |
rs775636816 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714107 | AGAATCAACTAAGAG[A/T]CTGGCATCTTTTTAA | 254065 |
rs775638823 | snp | C/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685491 | AATCTTGTTGTCTTT[C/T]TGGAACAACAGACTC | 254065 |
rs775645895 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702460 | CTGCCTCCAGAAAAT[-/A]AAAAACAGGCAACAA | 254065 |
rs775667195 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772842 | TGGAATCATCCCAGA[G/T]GTCCTTCAATTGGTG | 254065 |
rs775676860 | in-del | -/C | 0.0118403 | 0.0760259 | intron-variant | BRWD3 | GRCh38.p7 | X:80777144 | AAAGCACTCTTAAGA[-/C]CCCCCCCCACGAAAA | 254065 |
rs775682673 | snp | C/T | 5.41199e-05 | 0.00520164 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80689790 | GCATCAGTACTGTTT[C/T]GTTCTTCTGCTTTAA | 254065 |
rs775691065 | in-del | AGGCCAGGGGAGGGATAGCATTA/CG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772476 | CCTGTCGTCGGGTGG[AGGCCAGGGGAGGGATAGCATTA/CG]GGAGAAATACCTAAT | 254065 |
rs775706677 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80753807 | TGCATGTTCTTGTCA[C/G]CTTTGTCAAAGATCA | 254065 |
rs775707880 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80800993 | ATAACCTGAGGGCAG[A/G]TGAAATTAAGACAAG | 254065 |
rs775740224 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80716502 | TCTCCTTCTTCCTAG[C/G]CCCTGAAAACCTCTA | 254065 |
rs775753906 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725966 | TATATAACACATAAC[A/T]TGTTTACATGTTATA | 254065 |
rs775757386 | in-del | -/AA | 0.00371155 | 0.0429185 | intron-variant | BRWD3 | GRCh38.p7 | X:80731895 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 254065 |
rs775758099 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776313 | TCATTATTTACATTA[-/G]AAAAAAAATATGTTT | 254065 |
rs775761379 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80740845 | CATACTAACTCTGAC[G/T]GGCAAACATCTTGCA | 254065 |
rs775786494 | in-del | -/CAG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774481 | TTCTCCATCCTCACA[-/CAG]CAGTTCCTGAGTGAT | 254065 |
rs775792627 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807810 | AATCGTGTTTCACCA[A/G]TTCTCAAAAAGTGAT | 254065 |
rs775793534 | snp | A/C | 0.000164456 | 0.00906646 | intron-variant | BRWD3 | GRCh38.p7 | X:80728726 | CTTTTTGACCATTTT[A/C]ATTACTCTAAAAATA | 254065 |
rs775797440 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705336 | AAATGCTTCTTGGAT[A/G]AAGTATACTTTATCC | 254065 |
rs775807558 | snp | A/G | 2.27912e-05 | 0.00337566 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677026 | GCCTCTGGTCTTCCA[A/G]TTTCTTTTTCCATTG | 254065 |
rs775831154 | snp | C/T | 2.28235e-05 | 0.00337805 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692954 | CTGAACACTGTAACA[C/T]TGGAAAGAACTATCA | 254065 |
rs775834359 | in-del | -/TGTT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697969 | AACCTCACAAGCATC[-/TGTT]TGTTTGTTTTGAATT | 254065 |
rs775846264 | snp | C/T | 2.27996e-05 | 0.00337628 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717611 | ATTGACCACCACTCT[C/T]CTGCTCCACGCCATG | 254065 |
rs775846430 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786093 | CAAATTATGCACCTA[A/T]CCAGAGTAGCTTACC | 254065 |
rs775847805 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785547 | TAACTATACGAACGA[C/T]GGAAACATTTGAATA | 254065 |
rs775870259 | in-del | -/TCA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745154 | AAATAGCTATAATCT[-/TCA]TCACAGTGTAGTTCA | 254065 |
rs775875353 | snp | A/T | 0.00317376 | 0.039709 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672761 | GAAAGTTCCATCCCT[A/T]CCCCTAGAACTATTC | 254065 |
rs775879537 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737486 | CAGATGCAGAATCTA[C/T]GGATACAAAGGGTAA | 254065 |
rs775922512 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678958 | GACTGATGTTCTTAA[A/C]GGAAAAGGAAGAGAT | 254065 |
rs775939526 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80710848 | TTTTTTCTAAGCAAC[C/T]TCACTAAAACCATAT | 254065 |
rs775947564 | snp | C/T | 2.56331e-05 | 0.00357993 | intron-variant | BRWD3 | GRCh38.p7 | X:80723926 | GTAATTTTCAAATAA[C/T]AGATAGGCGGTAACT | 254065 |
rs775948142 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786652 | CCCAAGTAGCTAGGA[-/T]TACAGGCATGCACCA | 254065 |
rs775953909 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806338 | ATTCCTTAAAGGTTA[A/G]GCCTCACTAGTAATG | 254065 |
rs775985222 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786518 | CTTTTAATTTGCCTA[-/TA]TATATATATATATAT | 254065 |
rs775993469 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80717302 | CATGAGTTCTTAATA[C/T]TACTTGTATTCTTTT | 254065 |
rs776005911 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722490 | TAGCAGGAGGCATAC[A/G]TCATAGAGAGAACAG | 254065 |
rs776017083 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694441 | GAGAAGAGAGTCACC[A/G]TCCTCCAGACCCCAG | 254065 |
rs776021280 | snp | A/G | 0.000174551 | 0.00934049 | intron-variant | BRWD3 | GRCh38.p7 | X:80809426 | ACCCCCCCACCCCCC[A/G]ACACAGCTACCCACC | 254065 |
rs776042923 | snp | A/C | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671332 | TGTCTAAGATGAAAA[A/C]AAAAAACAAAACCTT | 254065 |
rs776047431 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682817 | CAAATATAGTATTCA[A/G]TGTTCTAAAAGGTAG | 254065 |
rs776061251 | in-del | -/TGTCTGTATAACATATAACATGTTTACATGT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726342 | CATGTTTACATGTTA[lengthTooLong]TATATCTGTATAACA | 254065 |
rs776061289 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80799136 | TGATAGTTAGACTGG[C/T]TGACCTGAAGAGCAA | 254065 |
rs776066324 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80790741 | TGAAGCATAACACAC[C/T]ACAAAATAATGTTGA | 254065 |
rs776074744 | snp | C/G | 0.000414321 | 0.0143871 | intron-variant | BRWD3 | GRCh38.p7 | X:80725114 | CAACACGAAATGTTT[C/G]GTTCATTTGGTAAAA | 254065 |
rs776084735 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669574 | AAATGATCTATTACA[A/C]AATTTGTTATGCAAA | 254065 |
rs776085124 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696259 | AGGAGTATGAATTAA[C/T]GTTCTTTAATCTCCT | 254065 |
rs776113034 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80760409 | AATTAAAACTGAATA[C/T]AATTCAAATAAAGGT | 254065 |
rs776131128 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758664 | GACATTAAAAAAAGA[A/G]TATAATATGGTGGTG | 254065 |
rs776143766 | snp | C/T | 3.49608e-05 | 0.00418081 | intron-variant | BRWD3 | GRCh38.p7 | X:80703640 | TAAAACACAGTTCTC[C/T]AATACATAAAACACA | 254065 |
rs776146197 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80789837 | TTTTTTTTTTTTTTC[C/T]GAAAAACTGTCAATT | 254065 |
rs776151755 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80768943 | CAGGGGTTGCAGTCC[C/T]AGTCTCTGATAAAAC | 254065 |
rs776152939 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781220 | GCTCCCATAAAATGG[A/G]AGGGGACCCAAAGGG | 254065 |
rs776155578 | snp | A/T | 3.00246e-05 | 0.00387446 | intron-variant | BRWD3 | GRCh38.p7 | X:80707394 | ATTAAAACTGTTCAA[A/T]AATTTTGACCAAATT | 254065 |
rs776175317 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721816 | CAAACACGAGGATAG[C/G]TAAATAGCTACCTCC | 254065 |
rs776182083 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80760210 | TTTTCTATTACACCT[A/G]CTATCCATCATATTT | 254065 |
rs776193540 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672714 | AATATTGGGGATGGG[A/G]TTAGCATTTAAAACA | 254065 |
rs776195672 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699700 | TGATTACGGAAAATA[C/T]CCACAAAGGGGAACT | 254065 |
rs776209963 | in-del | -/TA | 0.000121406 | 0.00779028 | intron-variant | BRWD3 | GRCh38.p7 | X:80709415 | TCAAATAAATAATAG[-/TA]TATATATATAACCTC | 254065 |
rs776261815 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80787218 | ATGAGAAATTAAAGA[G/T]TTACAAAAATAAAGA | 254065 |
rs776263951 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80750469 | GGCCAATGGATATAC[A/G]AAAAAATGCTCAACA | 254065 |
rs776279672 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80718861 | TACAAGCTAAAACTT[A/G]TATAAAACTCAGATG | 254065 |
rs776280300 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80749668 | ATGTCCATTCTACCC[-/A]AACAACATTTACAGA | 254065 |
rs776286108 | in-del | -/AA | 4.69677e-05 | 0.00484578 | intron-variant | BRWD3 | GRCh38.p7 | X:80709424 | TAATAGTATATATAT[-/AA]AACCTCTGAAGAACT | 254065 |
rs776292995 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795507 | TGTATATATGTATAT[A/G]TATGTATACATATAC | 254065 |
rs776315283 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80689095 | ACACAATCTAGCATA[C/T]GTGAGTCACTCATCC | 254065 |
rs776337491 | in-del | -/CCC | 2.35372e-05 | 0.00343046 | cds-indel, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691885 | CGTCTCTGGAATGAG[-/CCC]CCCCCCACTCTCCTT | 254065 |
rs776338576 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80728059 | AGTATAAAGACAACT[C/G]AGTTGAGTCAGAAGA | 254065 |
rs776344566 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767629 | AAAGCTGAAAATTCT[A/C]AAAACCAGAGAGAAA | 254065 |
rs776357311 | snp | A/C/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80713507 | GCATGCTCCTTAAGA[A/C/G]TCATCACCACTCCCT | 254065 |
rs776364298 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80779250 | AACCCAGGAGGTGAA[A/G]GTTGCAGTGAGTCGA | 254065 |
rs776390758 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80705468 | AAATGCTGAAGTGGG[A/C]TTGTTTTAAAACTGA | 254065 |
rs776418198 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781016 | CAATCAATGCTAAAT[A/T]AAAGCTTAGAGCAAC | 254065 |
rs776464457 | snp | A/C | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682539 | TGGCCTTCTCCTCTT[A/C]TGACTCTGGATTGCT | 254065 |
rs776465990 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688259 | AGCAAGTAGAACAAA[A/C]GATAGAGGGAGACTC | 254065 |
rs776466627 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713796 | TAACAATTTAATTTT[C/T]GGAACTGAAATCTAA | 254065 |
rs776470756 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796689 | CTGTCATGATGCTCC[A/G]GAAGAATGGTAATCA | 254065 |
rs776512456 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706401 | GAAGTGAGCCACCAC[A/G]TTCGGCAAATTTTTT | 254065 |
rs776515257 | snp | C/T | 2.28238e-05 | 0.00337807 | intron-variant | BRWD3 | GRCh38.p7 | X:80717564 | CTAAATGTTACCTTA[C/T]TGACTCACCTACTAA | 254065 |
rs776516940 | snp | G/T | 2.83242e-05 | 0.00376315 | intron-variant | BRWD3 | GRCh38.p7 | X:80692056 | ATTTTACTTTTAAAA[G/T]AATTATAATTCATTT | 254065 |
rs776521839 | snp | A/C | 2.30266e-05 | 0.00339305 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80724948 | CATGTTAAAGTAATT[A/C]CGAATTTTGGTCCCC | 254065 |
rs776524077 | snp | C/T | 0.000160838 | 0.00896623 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793603 | CTGATATCACAGTCC[C/T]AAATTCTGAAAATCT | 254065 |
rs776525446 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764543 | TGGTCTCGATCTCCT[G/T]ACCTCGTGATCTGCC | 254065 |
rs776545564 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710295 | AATATGGCTGGAGAC[C/T]ATATGGTGTTAGGCT | 254065 |
rs776554966 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80712510 | GCTACAACCTCCACC[G/T]CCCAGCCGCCTGCCT | 254065 |
rs776562148 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80679710 | AGAGAAGGTAGTCAA[C/T]AACATGCAATGATAT | 254065 |
rs776568323 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80807536 | CTTGAAGGAAAGATA[A/G]CTGAATTTAGATTTT | 254065 |
rs776575503 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80803992 | TGTTATATGCAGATG[A/C]AACTTCTTATAACAA | 254065 |
rs776598552 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800797 | CCTTTCCCTAGTTGC[C/T]CTTACAAAATGTTAA | 254065 |
rs776613500 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678858 | GAAGCCCTAATCCCC[A/G]AAGTGACTGCAGTTG | 254065 |
rs776613923 | snp | C/G | 3.66683e-05 | 0.00428168 | intron-variant | BRWD3 | GRCh38.p7 | X:80791813 | AGTTCAGGAAGGAAA[C/G]AATCAACAATCTGTT | 254065 |
rs776626375 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80739169 | TCATGAGAATTTGCC[A/C]GATTCTAGATACACT | 254065 |
rs776652349 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686922 | CTTCACGTTCATAAA[C/T]GAGGCTCAATAGTTC | 254065 |
rs776663610 | in-del | -/AGAATAA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733942 | AGGTAATCTTCTTTT[-/AGAATAA]TTAACCCATACTTTT | 254065 |
rs776673571 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80684910 | TCATCAAGAAGTAAA[A/T]TCTCCACATTTCCCT | 254065 |
rs776673955 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80787339 | AAAAACTCAGTACCT[C/T]CTTTTTGGGGAAATT | 254065 |
rs776687351 | snp | A/C | 0.00158814 | 0.0281345 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676034 | TACTTCAGTTCAGTA[A/C]AAGTCATGAAAGTTT | 254065 |
rs776699937 | snp | A/C | 2.33429e-05 | 0.00341627 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735187 | TCTCAGTAAATTTCA[A/C]CGGGCGATCTCTAAA | 254065 |
rs776704484 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756126 | TTCTCCCAGTTCAGC[A/G]GTTTATTTATTTATT | 254065 |
rs776710859 | snp | C/T | 2.28658e-05 | 0.00338118 | intron-variant | BRWD3 | GRCh38.p7 | X:80692927 | AGGCATAAAAGATCA[C/T]AAACATACTTACTGA | 254065 |
rs776717605 | snp | A/C | 0.00135303 | 0.0259747 | intron-variant | BRWD3 | GRCh38.p7 | X:80809419 | CCTTAGCACCCCCCC[A/C]CCCCCCGACACAGCT | 254065 |
rs776723018 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754980 | GCCACTGGACTCCAG[C/T]CTGGGCAACAGAGCG | 254065 |
rs776760643 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804656 | AGATTAACAAGAACT[C/G]TTCATTTAAACACAC | 254065 |
rs776772237 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708480 | ATTTCATATGGGTGG[C/G]GGTGGGGCATGAATG | 254065 |
rs776774368 | snp | A/T | | | intron-variant, utr-variant-5-prime | BRWD3 | GRCh38.p7 | X:80731112 | GTTTCCCTGAAAAGT[A/T]TTTTTAATAATTTAT | 254065 |
rs776780477 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726274 | AACACGTTTACATGT[-/TA]TGTCTGTATAACATA | 254065 |
rs776782654 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771511 | GGGGAAAGGATTCCC[A/T]GTTTAATAAATGGTG | 254065 |
rs776806990 | in-del | -/GA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766871 | GCCAACGGAAGCCTT[-/GA]GAGACAGCACCTGGA | 254065 |
rs776824474 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763571 | ATACACAAAACTCAA[C/T]TGCATTTCTATATAC | 254065 |
rs776826501 | snp | C/T | 0.000137273 | 0.00828358 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676789 | TTTAATTCGAGGCAG[C/T]CTACTGAAACGTCCT | 254065 |
rs776844527 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | BRWD3 | GRCh38.p7 | X:80731826 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 254065 |
rs776847466 | snp | A/G | 6.87679e-05 | 0.00586338 | intron-variant | BRWD3 | GRCh38.p7 | X:80688027 | TCACTGACACAGGAA[A/G]CCTGAAAACATATCT | 254065 |
rs776853330 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80677561 | TGGGAGAGGGAGGAG[A/C]ATATGGGGGTGGAAT | 254065 |
rs776853945 | snp | C/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810186 | CCTTCCCCCTGGGTT[C/G]ATCTTGAGGAACTTA | 254065 |
rs776862744 | snp | A/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792827 | TAAAACTTGGGAAAA[A/T]TCTGTAAAACACTGA | 254065 |
rs776901863 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753001 | TTGGCCATTTGCACG[A/T]CTTCTTTTGAAAAAT | 254065 |
rs776905439 | in-del | -/T/TT | 0.0454994 | 0.144908 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80791991 | TAAGGAATAGAGCAG[-/T/TT]TTTTTTTTTTAACCA | 254065 |
rs776917799 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80711929 | TAGGCATATGTTCTC[A/G]GGACTACTTCTTGAG | 254065 |
rs776948908 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745682 | ATGAAGGGAAAATAT[A/G]ACCAAAGCGACTACA | 254065 |
rs776949609 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716050 | TTCCCTATATGCAGA[C/T]ACCTATTAAAATAGT | 254065 |
rs776952720 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80702358 | GAGAAAAATAGTCCT[G/T]AGACAGGAGTCTCAT | 254065 |
rs776956989 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80794347 | CCCATCTCTACAAAA[A/C]ATACAAAAATTAGCT | 254065 |
rs776958729 | snp | G/T | 2.28658e-05 | 0.00338118 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716182 | GTGTAAGATGGCTTT[G/T]TCTTCTTTTCAACTG | 254065 |
rs776972445 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758231 | AAAAAATAAAAAAGT[C/T]AAACGAGGTCTCTGT | 254065 |
rs776983480 | snp | C/T | 2.28123e-05 | 0.00337722 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734145 | TAATTCAGCAATTTT[C/T]TCAGGAACCTCAGAA | 254065 |
rs776992097 | snp | G/T | 2.47225e-05 | 0.00351577 | intron-variant | BRWD3 | GRCh38.p7 | X:80722541 | CAAAATGTTTTAAAT[G/T]TACTTTTAGAGAAAA | 254065 |
rs776996889 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772633 | TAAAAAAAAATAAAT[C/G]ATCCTGAAGAAAGTA | 254065 |
rs777014920 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734720 | CAAAAAAAGGAAAAA[A/G]AAAAAGGTTAACTAA | 254065 |
rs777025601 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682734 | ACAGACAAAATATCT[G/T]TTCACTTGAAAAATT | 254065 |
rs777031555 | snp | A/G/T | 2.28749e-05 | 0.00338185 | synonymous-codon, stop-gained, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744091 | CGGGTGCACAAGTTC[A/G/T]AAGACACCATACTCT | 254065 |
rs777049901 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757169 | TTACTTTGATTAGTA[A/G]CTTAATTATTTCAAA | 254065 |
rs777060561 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767443 | ACCTCCAGCAAACAC[C/G]AACAGACCTGCAGCT | 254065 |
rs777066943 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80774318 | GTCACCCAGGCTGCA[A/G]TGTACTGGCACATCG | 254065 |
rs777071215 | snp | C/T | 4.49468e-05 | 0.0047404 | intron-variant | BRWD3 | GRCh38.p7 | X:80745553 | TATGTTACCATATTA[C/T]AAATTTTACACTCAC | 254065 |
rs777074415 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80717148 | TTAATCCTAATGAAA[C/T]TCTTTCACCCAATGA | 254065 |
rs777082698 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80693955 | GGAGCCAAATGTTAG[C/T]CACCAAGAAAATGGG | 254065 |
rs777089883 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758489 | GCAGATGGCCATTCC[A/G]ACCTCTGCCTAAACA | 254065 |
rs777101774 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676244 | AAAGCAAAAGAGGGC[A/T]ATTCTATTGAGATAA | 254065 |
rs777130580 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80693311 | CATAATTTAACTTTT[C/T]TCAATTAATTAGCAT | 254065 |
rs777133938 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80716857 | ATCATTTACTCCAAA[G/T]ACATTAATTATGTCT | 254065 |
rs777139887 | in-del | -/A | 2.66049e-05 | 0.00364716 | intron-variant | BRWD3 | GRCh38.p7 | X:80707529 | GAGCCAGCAATTAAG[-/A]TATATGGATATTACC | 254065 |
rs777162950 | snp | A/G | 2.28206e-05 | 0.00337784 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744208 | GTGTAGCAAGAAGGC[A/G]TCCATCATCTGTAGC | 254065 |
rs777163840 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768127 | CCTGAAAGTGACAGG[G/T]AGAATGGAATCAAGT | 254065 |
rs777168442 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800171 | GAAAGAAGGGCATTC[C/T]AAGCAAAGAGAAAGG | 254065 |
rs777185226 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754399 | TCAAAAATCTAGGAG[C/T]CCTTTGGAGGAGTCT | 254065 |
rs777210255 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698657 | GAGGTTGCAGTGAGC[C/T]GAGATCGCTCTACTG | 254065 |
rs777236044 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759868 | ATACTGTCTAGTCTG[C/T]AGTATAATCCCATAT | 254065 |
rs777237910 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80718148 | TTACAGTGTTTCTAG[A/C]TAAAACATCAATAAA | 254065 |
rs777240387 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706872 | CCATCTCTAAAAGAA[C/T]AGAAAATGAAATGAA | 254065 |
rs777241998 | in-del | -/TA | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80726045 | AACATGTTTACATGT[-/TA]TATGTCTATATAACA | 254065 |
rs777252676 | in-del | -/AAG | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80709345 | AATAATTTTCTATTA[-/AAG]AAGTGACCCTTAAAC | 254065 |
rs777256391 | snp | A/C | 2.30958e-05 | 0.00339814 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80808542 | AACTTTACTCACCAG[A/C]TCCTCGAAGCTTCTT | 254065 |
rs777259550 | snp | A/T | 2.74948e-05 | 0.00370765 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80700005 | TAAATTAACACTGTA[A/T]ATTTTCGATTTCCTT | 254065 |
rs777266100 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810127 | GAGCTCCGGAGTGAC[A/T]TTCCCTTCCTGTGAA | 254065 |
rs777270318 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80725916 | TACATATGTTACATG[C/T]CTATATGACATAACT | 254065 |
rs777278010 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757987 | GTGGATCACCTGAGG[-/T]TAGGGAGTTCGAGAC | 254065 |
rs777283062 | snp | C/G | 4.6644e-05 | 0.00482906 | intron-variant | BRWD3 | GRCh38.p7 | X:80696714 | ATACACACACTCAAA[C/G]AGAGACTCAGAGATA | 254065 |
rs777288164 | snp | C/G | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810888 | AACCTGATGAGACCA[C/G]AAATGCATTTTAAGT | 254065 |
rs777332869 | snp | G/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673936 | AAGTAATCAATGTGA[G/T]ACTAATTACAACACA | 254065 |
rs777334930 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701747 | AAATAATTGTAAGGG[C/T]TAAAAACCAATAATA | 254065 |
rs777339495 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786533 | ATATATATATATATA[C/T]GGAGTCTTGCTCTGT | 254065 |
rs777351957 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801954 | AATTCCCATTTGTTT[-/AA]AAAAAAAAGTGAATA | 254065 |
rs777361003 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791310 | ATACTTTGTGAGGGC[A/G]AACTTTAATATAAAT | 254065 |
rs777367671 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80693134 | CTACTTTTTGTTGAC[A/G]ACAGAAGTACTGTAT | 254065 |
rs777374143 | snp | C/T | 2.28415e-05 | 0.00337938 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717708 | TGACTACTATGTCTT[C/T]GAAGCCTGATGTTTG | 254065 |
rs777374299 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786723 | TTTCACCATGTTAGC[C/G]AACCTGGTCTCAAAC | 254065 |
rs777410358 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729378 | TCATTTCTATATTGC[A/G]ACTAATGGAAAGATA | 254065 |
rs777422768 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670849 | ATTGTAAAAAATCAG[C/T]CTACTTTTTTCCTAA | 254065 |
rs777442701 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80718147 | ATTACAGTGTTTCTA[C/G]ATAAAACATCAATAA | 254065 |
rs777475377 | snp | G/T | 2.29463e-05 | 0.00338713 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682620 | TAATCGCAGCATCAT[G/T]CTATAGATCTGAGAA | 254065 |
rs777491736 | snp | A/G | 5.46866e-05 | 0.0052288 | intron-variant | BRWD3 | GRCh38.p7 | X:80695900 | TTAAACAACAATTCT[A/G]TATTTACCAATCTGC | 254065 |
rs777493502 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777062 | TGGTCCTTAGTTGAT[C/T]ATGCTTAAACAAAAA | 254065 |
rs777503508 | snp | C/T | 2.31195e-05 | 0.00339989 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676926 | CACCTCCACCTCTTC[C/T]TCGACTCCCTCGTCC | 254065 |
rs777505435 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741205 | GAGAATGATGGTTTC[C/T]AGCTTCATCCATGTC | 254065 |
rs777514475 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737240 | GTAGATGCTCAAGTC[C/T]CTGATATAAAATGGT | 254065 |
rs777514484 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777951 | CCATCACACACAGCC[G/T]AAGTTTTAAATTTTA | 254065 |
rs777516622 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678721 | GCCAGTGGGGTCGGT[A/G]GGAAACAAGAGAGCA | 254065 |
rs777518163 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80800702 | CTAAATCAAATGCTG[C/T]GTTTTAATGGTTGCT | 254065 |
rs777532195 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80723487 | TACCTGGAAGGCAGG[C/T]ATAATATACGCAAAA | 254065 |
rs777535813 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698113 | TATACATTTTCTTTT[A/C]AGAAGTGTCTGTTCA | 254065 |
rs777536604 | snp | A/T | 2.31412e-05 | 0.00340148 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793575 | AAAAATAAGCTACTC[A/T]CCACTCCTTCCTCTG | 254065 |
rs777551187 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761942 | AGACACATTTGCCCA[C/G]AGGTACAATTAGAAA | 254065 |
rs777562740 | snp | A/T | 2.29187e-05 | 0.00338509 | intron-variant | BRWD3 | GRCh38.p7 | X:80717542 | GAATAAAGCTTTAAA[A/T]TTTTTTCTAAATGTT | 254065 |
rs777564239 | in-del | -/AC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802033 | AATATCTTTTGACAT[-/AC]ATTCATGTTTGTGTT | 254065 |
rs777602626 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80744928 | TAACTTCCCGAATAA[C/T]TTCCACTTCATTCGT | 254065 |
rs777623394 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751236 | TATTTCAAAATTGCT[A/G]AAAGAATAGATTTGT | 254065 |
rs777638901 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80710326 | ACTTACTGCTGGTTA[G/T]AATGATATGGGCCTC | 254065 |
rs777642979 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80790618 | AGAAGTTTGAAAGTA[C/T]ATGCTTAGTTAAAAG | 254065 |
rs777646209 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721003 | ACAAGTTTAACCACA[A/G]ATACCTAAAATGCTT | 254065 |
rs777652488 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799442 | ACGCTATTTGTTTTC[C/T]AAGACCATGGCTACA | 254065 |
rs777667683 | snp | A/G | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672713 | AAATATTGGGGATGG[A/G]GTTAGCATTTAAAAC | 254065 |
rs777679180 | snp | A/G | 3.6203e-05 | 0.00425443 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745725 | CCTGGCAGAGGTGAT[A/G]TTCACTGAAAAAAAT | 254065 |
rs777679309 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711362 | GAGGGGTTTTACTTA[A/G]CCCTATATAACGTGT | 254065 |
rs777683150 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735907 | TGTAAATATATATAT[G/T]TAAATACATGGACTA | 254065 |
rs777691761 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728585 | TTAGCAGGTATAGCG[C/T]GTGTCATCCCTATTT | 254065 |
rs777701042 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722294 | AACAACAGCTTCATA[C/T]ATATATAAGGTTTTC | 254065 |
rs777709501 | snp | A/G | 2.29941e-05 | 0.00339065 | intron-variant | BRWD3 | GRCh38.p7 | X:80688146 | TTAAAAAGGAAGAGT[A/G]GGAAAAGACGTTAAG | 254065 |
rs777709786 | in-del | -/A | 0.21999 | 0.248192 | intron-variant | BRWD3 | GRCh38.p7 | X:80715212 | CATTCAAAATCTCTT[-/A]AAAAAAAAAAAAACT | 254065 |
rs777717570 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735344 | GTACTATTCTCATCA[A/T]TTAGGTTAAAAATGC | 254065 |
rs777737340 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753651 | TATTATTTTTATAGT[A/T]GTGGGTATTACATTT | 254065 |
rs777742526 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764178 | TGAAAGAATAATGAA[C/T]GTTGACCTAAACCTT | 254065 |
rs777780460 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738101 | AGACAATTAAATATG[A/C]AATAGTATAATTTTA | 254065 |
rs777786181 | snp | C/T | 4.64269e-05 | 0.00481781 | missense | BRWD3 | GRCh38.p7 | X:80676718 | TCAGTGGACACAAAA[C/T]TGTCATTATCAGAAT | 254065 |
rs777821072 | in-del | -/ATT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751985 | TATTCATATTTCATT[-/ATT]ATTATTATTATTATT | 254065 |
rs777825462 | snp | C/T | 4.89572e-05 | 0.00494734 | intron-variant | BRWD3 | GRCh38.p7 | X:80735245 | ATCATGTTTGGCTAA[C/T]GGGCCAGAATGTTAG | 254065 |
rs777844232 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707220 | AAAAAGAATCTTATT[C/T]TATAGATGAAGAAAC | 254065 |
rs777858805 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782087 | AAACTGGAGAAATCA[C/G]TTACCTGATTTCAAA | 254065 |
rs777858945 | snp | A/G | 2.31583e-05 | 0.00340274 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723847 | TGAAAATTTACAATC[A/G]AACACCGCACCATGG | 254065 |
rs777862361 | snp | C/T | 4.85013e-05 | 0.00492426 | intron-variant | BRWD3 | GRCh38.p7 | X:80735101 | AAATATTCTAGATGC[C/T]CAAAACATTCCAGTT | 254065 |
rs777873861 | snp | C/T | 4.59263e-05 | 0.00479177 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722775 | CCGTGTGGAAGAACA[C/T]CTGATCTGGAATCTT | 254065 |
rs777877919 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726755 | AGACTGGCTCAAAAT[G/T]TAGTGTTAAGATTAG | 254065 |
rs777900746 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769940 | CTGATCCCACAGAAA[C/T]ACAAACTACTATCAG | 254065 |
rs777907667 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707817 | TTTTCAAAATGCCTA[A/T]ATGTCTCTGTCGAGT | 254065 |
rs777912555 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732995 | CTTAGCCAGGTGTGG[G/T]GGCATGCACCTGTAA | 254065 |
rs777918801 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789496 | TTCTCCTGCCTCAGC[C/T]TCCCCAGTAGCTGGG | 254065 |
rs777924171 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80715385 | AAAAAATGCAAATTC[A/T]GGGTCCATTACCTAG | 254065 |
rs777934156 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798472 | TAATATTATAAACCA[C/T]TCTTTTTGTTTAAAG | 254065 |
rs777938655 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80780438 | CCTAATATTACTACA[A/G]TACTGATTTCAGAAA | 254065 |
rs777964960 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80735293 | ATCAATTTAGCATCA[A/T]TATTATAGAAAAAAC | 254065 |
rs777974113 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80748728 | TTTTTCAAGTCTCTA[C/T]CTTGTCTATTTCTGC | 254065 |
rs777980967 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731013 | TGATGAACATCTCTA[A/T]ATAATCTTTGTACAA | 254065 |
rs777984364 | snp | A/T | 5.01115e-05 | 0.00500532 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677362 | TCCATCAAGGGAGTG[A/T]TCTAAATTAAAATGA | 254065 |
rs778019024 | in-del | -/ATCTAG | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697727 | CCACCACTGACGGGC[-/ATCTAG]ATTGATTCCATGTCT | 254065 |
rs778045099 | snp | A/G | 2.29566e-05 | 0.00338788 | intron-variant | BRWD3 | GRCh38.p7 | X:80681986 | ACACCAAAAACAAAA[A/G]ACATATTTACCAGGA | 254065 |
rs778053828 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687595 | CTGGCATTTGGGAAC[C/T]TGGCATTTGAATGGC | 254065 |
rs778059746 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80770685 | CACTCCCTTTGAAAA[C/G]TGGGACAAGACAGGG | 254065 |
rs778065879 | snp | A/G | 2.30017e-05 | 0.00339121 | intron-variant | BRWD3 | GRCh38.p7 | X:80733523 | AACAGATTTTTCGTT[A/G]AAATGGACTTATTTG | 254065 |
rs778077770 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80755002 | AACAGAGCGAAACTC[C/T]GTCTCAAATTAAAAA | 254065 |
rs778082237 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731755 | AAAAAATTAGCCAGG[C/T]GTGGTGGCGGAGGCC | 254065 |
rs778087210 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80745198 | AAAAAAAGTGATGAA[A/G]TCATTATTTAGGGAA | 254065 |
rs778092261 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720733 | TCACATTCAACCACT[C/T]ACTCACTGAATCACC | 254065 |
rs778111956 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710240 | CCTGTGTCTTCTCTT[A/G]TATCTCTAATTGGAA | 254065 |
rs778114638 | snp | C/T | 5.12978e-05 | 0.00506422 | intron-variant | BRWD3 | GRCh38.p7 | X:80809403 | CGCTAAGCCCCCATT[C/T]CCTTAGCACCCCCCC | 254065 |
rs778125822 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764074 | CATAAATTTTCTTAA[A/C]TGATTTTTAACAAAG | 254065 |
rs778138833 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805402 | CATATATGCAGTATA[C/G]GTGGCCATGCAACCC | 254065 |
rs778143645 | snp | C/T | 2.31198e-05 | 0.00339991 | intron-variant | BRWD3 | GRCh38.p7 | X:80686815 | TTTAGCATGGACATT[C/T]ATGGGAAATTATCAT | 254065 |
rs778146768 | snp | G/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792578 | CCAAATAAACTCAAT[G/T]AAGAATTTCCTTAAA | 254065 |
rs778152376 | snp | A/G | 4.76315e-05 | 0.00487991 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691167 | ACAGCAAAAGGGCTG[A/G]CAAAATCTACAAAAT | 254065 |
rs778169655 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757996 | CCTGAGGTAGGGAGT[C/T]CGAGACCAGCCTGAC | 254065 |
rs778171406 | in-del | -/AACAA | 0.00159109 | 0.0281605 | intron-variant | BRWD3 | GRCh38.p7 | X:80740731 | TCCAGCATGGGTGAC[-/AACAA]AACAAAACAAAACAA | 254065 |
rs778217661 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703221 | TAAAGCCAATTATTT[C/T]TATGACTTCACAAGC | 254065 |
rs778222646 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794290 | GCAGGTGGATGGCTT[A/G]AGCCCAGGAGTTTGA | 254065 |
rs778254001 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80690572 | TCGTCAGTAGGAGAC[C/T]TGGATGACAGAGGGA | 254065 |
rs778257710 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725642 | TATGTCTATATAACA[C/T]ATAACATGTTTACAT | 254065 |
rs778269866 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712738 | CCCATCGTCTGAGAT[A/G]TGGGGAGCGCCTCTG | 254065 |
rs778287952 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80765837 | TGTATTTCAGTTGTA[C/T]GCAAACAGATATATC | 254065 |
rs778288312 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721303 | TGATAAATTAGACTT[C/T]CTTATTCATTTCTTT | 254065 |
rs778288469 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | BRWD3 | GRCh38.p7 | X:80712329 | GGTTTTCGTATTTTT[C/T]TGGTGGAGACGGGGT | 254065 |
rs778308279 | snp | A/T | 2.42081e-05 | 0.003479 | intron-variant | BRWD3 | GRCh38.p7 | X:80744304 | GCAGAAATTCACAAT[A/T]CCCCCACCCAAAAAA | 254065 |
rs778323529 | snp | C/T | 2.65844e-05 | 0.00364575 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691957 | ACAGGAACACCAGCA[C/T]CAACTTCATCTGGAA | 254065 |
rs778328654 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80753394 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 254065 |
rs778338855 | snp | A/T | 2.61161e-05 | 0.0036135 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691947 | TTCCTGGGAGACAGG[A/T]ACACCAGCACCAACT | 254065 |
rs778347082 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678473 | ACAAGACATTTTTTT[A/T]AAAAAAAGAAATAAA | 254065 |
rs778347235 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763439 | TCTAGCTCAAACCTA[C/T]CTAGAACATAAATCT | 254065 |
rs778355366 | snp | A/G | 3.92157e-05 | 0.0044279 | intron-variant | BRWD3 | GRCh38.p7 | X:80709613 | AAATTTTAAAAAAGG[A/G]AAAGCTCAGTAAACA | 254065 |
rs778355478 | in-del | -/A | 0.124444 | 0.216185 | intron-variant | BRWD3 | GRCh38.p7 | X:80736091 | TGATGGACAAAACTT[-/A]AAAAAAAAAAAAATC | 254065 |
rs778387206 | in-del | -/TG | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715694 | ACAACTATTCAATTC[-/TG]TCTTACAGCCTGAAA | 254065 |
rs778388061 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80703303 | TGCCAGGACCTACAA[A/G]GGATACAAAGATTAA | 254065 |
rs778406484 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747399 | CCCCCACACTAAGTC[A/G]TGACAAACAAAAATA | 254065 |
rs778413523 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80759563 | TAAAGCAAAATATTA[C/T]TCTCTCCAGCTCTTA | 254065 |
rs778419234 | snp | C/T | 4.56981e-05 | 0.00477985 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681409 | TGGCTATTTCCACTT[C/T]GGCTATATCCACCGA | 254065 |
rs778435191 | snp | A/C | 2.35869e-05 | 0.00343407 | intron-variant | BRWD3 | GRCh38.p7 | X:80734268 | CAAGGAACCTTAAAA[A/C]CCCTCTCATTACTTC | 254065 |
rs778468070 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80713390 | TGATCTATGACCTTA[A/C]CCCCAACCCTGTGCT | 254065 |
rs778479850 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678663 | CTTGAGATGTTCAAA[A/C]ATTTAAAGATAAAGA | 254065 |
rs778486691 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80795194 | AATCCCTGAGGTGTT[G/T]CATAAATACTTAATT | 254065 |
rs778504509 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80702105 | GGCAAGACAATGAAG[G/T]CTTAATATTAAGATG | 254065 |
rs778509568 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80775404 | CTTTACTTGACACAA[C/T]TGGGGCCCAGAGTAT | 254065 |
rs778512223 | in-del | -/A | 0.0465453 | 0.14528 | intron-variant | BRWD3 | GRCh38.p7 | X:80800574 | TACAAATACTTGTAC[-/A]AAAAAAAAAAACAAG | 254065 |
rs778561896 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743892 | AAAAAAATATCTTGC[G/T]GCAGGGTAGGAGCAA | 254065 |
rs778573132 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758131 | TTGAACCTGGGAGGC[A/G]GAGGTTGTGGTGAGC | 254065 |
rs778581565 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80707570 | TTTCTAATTAAAAAA[A/C]CACTACCTGTTTTAT | 254065 |
rs778590266 | in-del | -/AT | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80725904 | ATATAACATGTTTAC[-/AT]ATGTTACATGCCTAT | 254065 |
rs778595512 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80774109 | GAAATGTTAATCAAC[C/T]CTGTAATTCTCTTAT | 254065 |
rs778605308 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752788 | TCCTGCCTTAGCCTC[C/T]TGAGTAGCTGGGATT | 254065 |
rs778617181 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763343 | TTCTTAAAATGAGAG[A/G]AAAATGAAAAAAATC | 254065 |
rs778623743 | snp | C/G | 2.43677e-05 | 0.00349045 | missense | BRWD3 | GRCh38.p7 | X:80676623 | GTTAATAATTCCATC[C/G]CATGAGATGGCTAAC | 254065 |
rs778643284 | snp | A/G | 2.30835e-05 | 0.00339724 | intron-variant | BRWD3 | GRCh38.p7 | X:80716289 | GTAACAGAAAATCAA[A/G]AAGAAAACCAATCAT | 254065 |
rs778650969 | snp | A/G | 2.40402e-05 | 0.00346692 | intron-variant | BRWD3 | GRCh38.p7 | X:80687006 | CTCGGCATTTGACCT[A/G]CAGATTTTAATAGAG | 254065 |
rs778664390 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726392 | TCTGTATAACATAAC[A/G]TGTTTACATATGTTA | 254065 |
rs778665816 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776124 | TGCAATAAGAAATAA[C/T]TTAACAGCAAAAATT | 254065 |
rs778666616 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701346 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 254065 |
rs778688178 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785721 | AAGTAGTTTCTAAGG[A/T]TAAAAATAGGAAACT | 254065 |
rs778715995 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:80682359 | TAGGAAACAAACAAA[A/G]AAAGACCTCTTGGGA | 254065 |
rs778718534 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:80671933 | CATTTGTAGTACTGC[C/T]TAATGTGTATCTGGT | 254065 |
rs778719840 | snp | C/G | | | | | GRCh38.p7 | X:80703853 | CATAACTTTTACATA[C/G]GTCCCTTGACTACCA | 254065 |
rs778722699 | snp | C/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:80758950 | TTCCTAATATCCCCT[C/G]AAGAAAAACACTCCT | 254065 |
rs778724047 | snp | A/G | 2.30298e-05 | 0.00339328 | | | GRCh38.p7 | X:80723811 | ATGAGAATCTGTGCA[A/G]GCAAAATGGTTTCCA | 254065 |
rs778741032 | snp | A/G | 4.72891e-05 | 0.00486234 | | | GRCh38.p7 | X:80703605 | CTTTCTAAAACATAA[A/G]TACACGAAAAGTATA | 254065 |
rs778752032 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:80671108 | GTAGGTAATCTTACT[A/G]TACATTTTAAAATGT | 254065 |
rs778759157 | snp | G/T | | | | | GRCh38.p7 | X:80738612 | GATACAGAGTTGCTG[G/T]GCACACAGTGGAGGG | 254065 |
rs778775418 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728538 | TAACTACCAGACTTA[A/G]AAAAGATCTTGAAAA | 254065 |
rs778777637 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80717959 | TTATTGAGAAATGTT[C/T]AAAATTTCTATAATT | 254065 |
rs778793053 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789567 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 254065 |
rs778798369 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783775 | GTCATTTATAACAAC[-/A]ATGGCTAGTACTGGA | 254065 |
rs778813011 | snp | C/T | 5.08669e-05 | 0.0050429 | intron-variant | BRWD3 | GRCh38.p7 | X:80703445 | TTAGTGCTCTTGAGG[C/T]TCCACAGAAAAAGGT | 254065 |
rs778828235 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80768604 | ATGGAAAGAAACAAC[C/T]GGTACCAGCCACTGC | 254065 |
rs778841115 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730324 | GGAAACAACCCAAAT[A/G]TCCATCAACGGGATA | 254065 |
rs778846208 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80709234 | CAAGACAGCATCTGA[A/G]GTACAAATCCAAGAC | 254065 |
rs778877473 | in-del | -/TAATTAATAGCC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770103 | CTAAAATTGAGGCAA[-/TAATTAATAGCC]TACCAACCAAAAAAA | 254065 |
rs778878914 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80768221 | TTCAAATTCAGGAAA[C/T]AGAGAGACCACCACA | 254065 |
rs778886417 | in-del | -/TT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80706411 | ACCACGTTCGGCAAA[-/TT]TTTTCTTTATATCCT | 254065 |
rs778912328 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800019 | AATAGAAACAAATTA[A/C]GCTGCAAGTGCCCAG | 254065 |
rs778922582 | snp | C/T | 2.28532e-05 | 0.00338025 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744109 | GACACCATACTCTTA[C/T]TACCTTATCACAGCT | 254065 |
rs778951150 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714348 | TTCTCCTGCCTGCCT[C/T]AGCCTCCCGAGTAGC | 254065 |
rs778957409 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706258 | GGATTACAGGCCTCT[A/G]CCACCACATCCGGGT | 254065 |
rs778965308 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801929 | AAGACATATGAAAGA[C/G]TCACAATAAAATTCC | 254065 |
rs778974861 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781529 | AAAACCCAAGTGCTG[C/T]TGGGGAGGTTGGCCG | 254065 |
rs778977592 | snp | A/T | 0.0297427 | 0.118265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713695 | TGATCAATAAAAAAA[A/T]AAAAAATAAAAAAAA | 254065 |
rs778985457 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80784578 | GTGTGTGTTGTTCCC[C/G]CGCCCTGTGTCCATA | 254065 |
rs778990210 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757057 | CCCATACTCCTAGCC[-/T]GATGTATTCACTATA | 254065 |
rs779003229 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80765594 | AGTGTTATGAAATAT[C/T]ATTCCTCCTTATTTT | 254065 |
rs779023705 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734507 | AATGCAATGTTCCAA[A/C]ATTATTTATAAGACA | 254065 |
rs779033979 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680212 | CTGAACATGTTAGAA[C/T]TTTCTCTAAATACAT | 254065 |
rs779035596 | snp | C/T | 4.56845e-05 | 0.00477914 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681384 | AAATGATTTGGCTTT[C/T]CCTGGGTCATGGCTA | 254065 |
rs779038443 | in-del | -/AC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80699357 | GAAAACCAAAATGAA[-/AC]ACACATAAACCTAGG | 254065 |
rs779040607 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80710101 | AGCTCATCAGAAAAA[A/G]ATTCTCCATATTGAC | 254065 |
rs779054413 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724097 | CATTGCTAGCAAGGA[A/C]ATACCTCATGAAATA | 254065 |
rs779059081 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80790509 | AATGAATTTAAAAAC[A/G]TCAGTGCCAGGGCCA | 254065 |
rs779080932 | snp | A/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80808364 | AGCAGGGCCAAGGGG[A/T]GGGCAAGGTACCCTT | 254065 |
rs779083677 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80772965 | ATGATCAGGAAATTA[C/T]GCTGAGCAAGAGAAA | 254065 |
rs779084762 | in-del | -/TA | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792786 | TATCAAATACCACTT[-/TA]TGTTTGACATATTGA | 254065 |
rs779094763 | snp | A/G | 6.86507e-05 | 0.00585838 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728838 | TAACTGTGGTATCAT[A/G]GCGATCCCAGGCCAC | 254065 |
rs779096311 | snp | A/G | 2.28355e-05 | 0.00337894 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722752 | ATCACGAATAAGAGG[A/G]CGATAATCCGTGTGG | 254065 |
rs779109231 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80741918 | TCTTTAGTTTAATTA[C/G]ATCGCATTTGTCAAT | 254065 |
rs779118562 | snp | A/G | 2.82781e-05 | 0.00376009 | intron-variant | BRWD3 | GRCh38.p7 | X:80744287 | AATAGGTTTATAATG[A/G]AGCAGAAATTCACAA | 254065 |
rs779147940 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80706893 | ATGAAATGAAGAAAC[C/T]GTAATAATATAAAAG | 254065 |
rs779169026 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80690418 | GCCAAGAAGAGCAAG[-/A]AAAAAAAAACAGATT | 254065 |
rs779176211 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80787987 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 254065 |
rs779185612 | snp | A/T | 2.2865e-05 | 0.00338112 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691100 | GGTATTGAGGTCAGT[A/T]GGATAAGCAACTACA | 254065 |
rs779193440 | snp | C/G | 4.62524e-05 | 0.00480875 | synonymous-codon, intron-variant | BRWD3 | GRCh38.p7 | X:80684058 | GTTGTTGAATATTTG[C/G]CGAACATCCTTATAA | 254065 |
rs779195218 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80746790 | TAGAACCATGCCACA[A/G]TCAAAAATATGAAAT | 254065 |
rs779196439 | in-del | -/AAA | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669214 | GTGTTCAGCAGTCTT[-/AAA]TTTTTGAAAAAAACG | 254065 |
rs779216398 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769763 | CAGAACTGAAGGAGA[C/T]AGAGAGAGAAAAAAA | 254065 |
rs779230424 | in-del | -/AT | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80726288 | TTATGTCTGTATAAC[-/AT]ATAACACGTTTACAT | 254065 |
rs779265596 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728258 | CACTACCCATGTGAT[C/T]TCTGCTATTAATCCT | 254065 |
rs779274138 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697693 | TCCATGATGTCTATG[C/T]ACATTTTCTTTATCC | 254065 |
rs779281794 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670738 | ACCAAAAATTTTTAA[C/T]GTAAGATTTTTATAT | 254065 |
rs779285503 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80770630 | GCTACTTATGACAAA[C/T]CCACAGCCAATATCA | 254065 |
rs779307863 | in-del | -/T | 3.29511e-05 | 0.00405887 | intron-variant | BRWD3 | GRCh38.p7 | X:80691037 | TTTTATAATAAGTGA[-/T]TAAAAAAAAACAGAC | 254065 |
rs779335893 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739617 | ACAGTATCATAAATA[C/T]TTTTCATTATTTAGT | 254065 |
rs779356105 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710061 | CAGTATTGGTTGCAT[G/T]GAAAAGGGCACCATC | 254065 |
rs779365055 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792889 | ATTACTGAGGCCCGG[C/T]GCAGTGGTTTACGCC | 254065 |
rs779374055 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80757855 | ATAACATTGGTTTAC[C/T]TCTTACTAGAAGCTA | 254065 |
rs779397700 | in-del | -/AGAC | 0.00106326 | 0.0230326 | intron-variant | BRWD3 | GRCh38.p7 | X:80730447 | GAAAGAAAGAAAGAA[-/AGAC]AGACACAGTTAACAC | 254065 |
rs779403451 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711240 | AACATTGAGGGCTAA[A/C]CTCTGATCTTTTATT | 254065 |
rs779406146 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80803438 | AATGATAAATCTCCA[A/G]AAGGATTTTAAATCA | 254065 |
rs779406364 | snp | A/C | 0.0173306 | 0.0914601 | intron-variant | BRWD3 | GRCh38.p7 | X:80720572 | AAACAAACAAACAAA[A/C]AACCAAAAAACCTAA | 254065 |
rs779423570 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719745 | ATAAATTTCTACACA[A/G]ATGATTAAAAACAGC | 254065 |
rs779427655 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80726691 | AGAGTATCCTACCAT[A/C]TTACGATTATGGACA | 254065 |
rs779429262 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80739096 | TCGGTTAGAAGTCTA[C/T]TTCAATAATCTAGAC | 254065 |
rs779455186 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80803214 | CCTACCAAAAGGAAA[A/G]TGTTTATTAATCAAT | 254065 |
rs779475345 | snp | C/T | 2.31372e-05 | 0.00340118 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80729966 | CTTCCATTCTTGTTG[C/T]TGATACTGCCAAATT | 254065 |
rs779489497 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770217 | AACTAGTCCAATCAA[C/T]AGAAAAAGAGGGAAA | 254065 |
rs779500808 | snp | A/C | 3.03481e-05 | 0.00389527 | intron-variant | BRWD3 | GRCh38.p7 | X:80730044 | AGTTAAAATAACTTT[A/C]TTAATTTTCTCAAAA | 254065 |
rs779508030 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80747924 | GATGCATTTTGTTTC[C/T]TTCATTTTCATTTGT | 254065 |
rs779512264 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712274 | CTGCCTCAGCCTGCC[A/G]AGTGCCTGTGATTGC | 254065 |
rs779514007 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763969 | AATGTTAAGGCTTAC[C/T]ACATAGCTACAGAAA | 254065 |
rs779531448 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80712178 | CTCTCCCCTCTCCCC[A/T]CGGTATCCCTCTGAT | 254065 |
rs779534796 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80686699 | GAAGACACAATTACA[-/T]TTTTTTTAAAAATCA | 254065 |
rs779548263 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80762452 | TATATCAGCAATGTT[C/T]ATCTCCCACCAAATA | 254065 |
rs779572835 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675506 | AGGTGGTAGAGCATA[A/C]TATATTTATGAAACT | 254065 |
rs779579393 | snp | A/G | 6.06575e-05 | 0.00550682 | intron-variant | BRWD3 | GRCh38.p7 | X:80809320 | CTGGGGAAGAGGGGG[A/G]AAAAGAGGTTCAGAG | 254065 |
rs779581094 | snp | A/C | 1.64751e-05 | 0.00287007 | intron-variant | BRWD3 | GRCh38.p7 | X:80707510 | TTCATCTTCCTACAA[A/C]AAAGAGCCAGCAATT | 254065 |
rs779603401 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804573 | GAGACTCCTAAAAAT[A/G]ATTTAAAAATCTTAA | 254065 |
rs779606491 | in-del | -/ACAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750859 | CAATGTGTTTTATAC[-/ACAC]ACACACACACACACA | 254065 |
rs779631172 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698416 | AAGGTTAGGATAAAA[A/G]GTAAGAACTTGGCCG | 254065 |
rs779652374 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80692711 | CAAAAGAGGTAGCAA[A/T]AAAGTGTTTAGTTAT | 254065 |
rs779658903 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80784620 | TTCAGCTCCCACTTA[C/T]GAGTGAGAACATGCA | 254065 |
rs779665583 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80770042 | TACACCCTCCCAAGA[C/G]TAAACCAGGAAGAAC | 254065 |
rs779666955 | snp | A/G | 2.35682e-05 | 0.00343272 | intron-variant | BRWD3 | GRCh38.p7 | X:80716110 | AGCCTATTATCTACA[A/G]ATATCTGCAAATAGT | 254065 |
rs779674972 | snp | A/C | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792352 | TGCCAGGGAAAATTC[A/C]GGCATATTTATACTT | 254065 |
rs779704950 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80731328 | GACCACAATAATGTA[A/T]TTTCTCCTTAATGGA | 254065 |
rs779713508 | in-del | -/TCA | 0.0117643 | 0.0757875 | intron-variant | BRWD3 | GRCh38.p7 | X:80744296 | TAATGAAGCAGAAAT[-/TCA]TCACAATACCCCCAC | 254065 |
rs779725033 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773152 | ACTTAAAACTTCTTT[A/G]TCTTGACTGTGTTAG | 254065 |
rs779730178 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772378 | TAAGGACAGAAAACC[A/G]AACACCGCATGTTCT | 254065 |
rs779760562 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80753233 | GGACTTCAGTAAGTC[C/T]CATTTGTCTATTTTT | 254065 |
rs779770203 | snp | C/G | 2.33552e-05 | 0.00341717 | intron-variant | BRWD3 | GRCh38.p7 | X:80734067 | AAAGAAATGAAATAA[C/G]CTTTCCAAGGATGTT | 254065 |
rs779787840 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722944 | TTAGGTAGAAGAGAA[C/T]TGAATTACCTAAATG | 254065 |
rs779789915 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747122 | GGTACCCTAATTTGG[A/G]ACTTCAGAAATCTTC | 254065 |
rs779797139 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758018 | CAGCCTGACCAACAC[A/G]GTGAAACCCCGTCTC | 254065 |
rs779800467 | in-del | -/AAG | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80724380 | ATGAGAATTATTCTT[-/AAG]AGGATATTAGTATTT | 254065 |
rs779815152 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80794148 | GTGCCACTGTACTCC[C/T]GTCTGGGCAACACAG | 254065 |
rs779834040 | snp | C/T | 8.54299e-05 | 0.00653511 | intron-variant | BRWD3 | GRCh38.p7 | X:80809079 | ATATGAGGAGCAGCT[C/T]GGGCCATCAACCCAT | 254065 |
rs779852728 | snp | A/G | 8.72981e-05 | 0.00660617 | intron-variant | BRWD3 | GRCh38.p7 | X:80703429 | TTCAGACTGATTAAA[A/G]TTAGTGCTCTTGAGG | 254065 |
rs779856353 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758059 | ACAAAGTTAGCCAGG[C/T]GTGATGGCGCATGAC | 254065 |
rs779859757 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762434 | GAGTGCTTCATGTTT[A/G]AATATATCAGCAATG | 254065 |
rs779859912 | snp | A/G | 2.28061e-05 | 0.00337676 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719613 | GCTCTCATCTTGGTC[A/G]TTGGTTTGCTGCCCA | 254065 |
rs779860829 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678247 | ATATTTCCTTCTAGA[A/G]AAACCTTTAATTTCA | 254065 |
rs779870709 | snp | A/G | 6.83846e-05 | 0.00584702 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722708 | TGAGGAGCTTGTTGG[A/G]TTTGTTCATCCAATA | 254065 |
rs779872726 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767076 | AGGCATCCACCATTG[C/T]TGAGGCTTAAGTAGG | 254065 |
rs779887119 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80743829 | GAACTTTTTAAATCA[C/T]CTTTTTAGTTATTTA | 254065 |
rs779929528 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80691738 | GTACAGTGAGAAACT[A/G]CATATCCTTCTGTAG | 254065 |
rs779932321 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724282 | TTTTACCAATAAAAG[-/AC]AGAGGATCTGTCTTT | 254065 |
rs779941310 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810002 | GAGCCTAGACTCTCC[C/T]GGAGCCCGATGGTTG | 254065 |
rs779944119 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742932 | AACTTCCAGCACTAT[G/T]TTGAATAGGAGTGGT | 254065 |
rs779958182 | snp | C/T | 2.28624e-05 | 0.00338093 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681350 | TCCTACCTTGTTTAA[C/T]TGGCAAAACTCTATT | 254065 |
rs779961217 | in-del | -/ACACAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696520 | ATCCATAACATAAAT[-/ACACAC]ACACACACACACACA | 254065 |
rs779978233 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715568 | ATCATATTTTGCTCC[C/T]AAATGATTTGGTAAG | 254065 |
rs780002960 | in-del | -/TTATG | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80725619 | TTGAAAACCAATGCT[-/TTATG]TTATATGTCTATATA | 254065 |
rs780004570 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714757 | CAAAGGCACATAGAC[A/G]CACACAAATTCATGC | 254065 |
rs780007603 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80797947 | AAAAATACAAAAAAT[C/T]AGCTGGGTCTGGTTG | 254065 |
rs780018638 | in-del | -/GTGTGTGTGTGT | | | utr-variant-3-prime, cds-indel, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676333 | TCTGTGTTGTGTTTC[-/GTGTGTGTGTGT]CTGTGTGTGTGTATG | 254065 |
rs780019778 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80789522 | CTGGGACTACAGGCG[C/T]GTGCCACCACGCCCA | 254065 |
rs780026093 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687939 | TAATAAATATTATCA[A/G]TGAGCATACCTAATA | 254065 |
rs780039910 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767928 | ATGAGAACTACGTGA[C/T]GCATGCAGAAGCTTC | 254065 |
rs780043025 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800698 | TAACCTAAATCAAAT[-/G]CTGTGTTTTAATGGT | 254065 |
rs780056223 | snp | G/T | 2.69818e-05 | 0.0036729 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80696856 | ACAATCTTAACAAAC[G/T]CTTGCTCCTATTCAT | 254065 |
rs780076797 | snp | C/T | 4.69043e-05 | 0.00484252 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80677265 | TATCTTCTCCTCCCA[C/T]GTTTTCATCTTCTTC | 254065 |
rs780094827 | in-del | -/TA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680136 | ATATAAAATAAAATC[-/TA]TATATTCTAATAAAA | 254065 |
rs780095150 | snp | A/G | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671023 | GAATGTTCCTGTTAG[A/G]GCATTCAGATCATCT | 254065 |
rs780097506 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80723310 | ACAGCTAATAAAACA[C/T]AAAGACCAATTAAGT | 254065 |
rs780116011 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722348 | TCTGCTTGATGCTTA[C/T]GTTTGTCCTAACCCA | 254065 |
rs780118914 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80688679 | AGTAGCTCATGAGAT[A/G]TTGGTACTCCTTTCT | 254065 |
rs780135681 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80765278 | CAGTTACCATATTGA[C/T]TGACACTGACTACTG | 254065 |
rs780140196 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805292 | GAAGAAATTCAATTT[A/G]TCATTACCTTAATAT | 254065 |
rs780146071 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670390 | TAAATTGTCAAGAAC[A/G]TATAATTGAGAGAGG | 254065 |
rs780162255 | snp | C/G | 0.00017252 | 0.00928602 | intron-variant | BRWD3 | GRCh38.p7 | X:80690110 | GTGAAAGAAAAAATA[C/G]TCTGTTAGCCTTGGC | 254065 |
rs780165962 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713487 | TAAACAGATGCTTGA[A/G]GGCAGCATGCTCCTT | 254065 |
rs780178361 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80767980 | GAAGGAAGGGTGGTT[A/G]TCAGTGACTGAAGAT | 254065 |
rs780192841 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80807168 | AGACTTAAGTCCAAC[A/G]GAAAGACTGACTACA | 254065 |
rs780239024 | snp | A/G | 3.38518e-05 | 0.00411397 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80791978 | AGAACAAAGGTTGCT[A/G]AGGAATAGAGCAGTT | 254065 |
rs780242549 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80782346 | ATCTCTCGCCATATA[C/T]AAGAATCAAATCAAA | 254065 |
rs780259812 | snp | A/T | 4.58327e-05 | 0.00478688 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691064 | AGACCTGTAAAAGCG[A/T]TTTTCAAGTCTCCGC | 254065 |
rs780292999 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808164 | CTAATCCGGAACTCC[A/G]GGCTGTTACCAACGC | 254065 |
rs780294999 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749414 | AACTGCCAAACTTCT[C/T]GATGAACTAACATCT | 254065 |
rs780309638 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700158 | CCTCTTCTGTTTGCA[A/G]AAAGAAATAATTATA | 254065 |
rs780313239 | snp | A/G | 5.07022e-05 | 0.00503473 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80736066 | GTGAGGTATCTGTTT[A/G]TGCCTTTAGTTGATG | 254065 |
rs780321704 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80796154 | TTTTTTTTTTGAGTC[A/G]GAGTCTCGCTCTGTC | 254065 |
rs780359957 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80704995 | AATATCATCCAGGCA[C/T]GGTGGCTCACACCTG | 254065 |
rs780363050 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733757 | TTTATTATGTCCTCC[A/T]TAATAAGACAGCACA | 254065 |
rs780366978 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80741736 | TCTCTTCATATCCTT[C/T]GCCTACTTTTTGACG | 254065 |
rs780387304 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80691547 | TCCAAAGTCAGGCTC[A/G]GGAATAGCTAGAGAA | 254065 |
rs780387370 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80717555 | AATTTTTTTCTAAAT[A/G]TTACCTTATTGACTC | 254065 |
rs780394228 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80778933 | GAACCTGGGAGGTGG[A/T]GTTTGCAGTCAGCCA | 254065 |
rs780398965 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | BRWD3 | GRCh38.p7 | X:80787807 | AGACACTGGTAGGCC[A/G]GGCGTGGTGGCTCAC | 254065 |
rs780411718 | snp | C/T | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811171 | TTGACAAAACAAATA[C/T]GAATAATTGATACAA | 254065 |
rs780417849 | in-del | -/ACTTC | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80797388 | AGTTGTTACATAAAA[-/ACTTC]ACTTAACTACCCTAG | 254065 |
rs780436741 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693651 | TGGCAGCATTTTGCC[C/T]ATGCCCTAAGATCTG | 254065 |
rs780439683 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80680865 | ACGGGCTGGAGTGCA[A/G]TGGCACAATCACAGC | 254065 |
rs780446374 | snp | C/G | 6.84806e-05 | 0.00585112 | intron-variant | BRWD3 | GRCh38.p7 | X:80682447 | AGAACAAAAAATGTT[C/G]CATCAATGTAATGAT | 254065 |
rs780448211 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755624 | TCTATTACTCCACCT[C/T]TGGGCATCTATCCTG | 254065 |
rs780450269 | snp | C/T | 2.3176e-05 | 0.00340404 | intron-variant | BRWD3 | GRCh38.p7 | X:80693092 | GGATGCTCTTGAGAA[C/T]ATTAGCTCTGTTCCC | 254065 |
rs780453002 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741156 | TGAGTGAGAACATGC[A/G]GTGTTCGGTTTTTTG | 254065 |
rs780510412 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685041 | ATATATCTTATTTTC[C/T]TAAATCATAAAAAAA | 254065 |
rs780553087 | in-del | -/TTTGACGAAAGTCAAAAG | 2.30521e-05 | 0.00339493 | intron-variant | BRWD3 | GRCh38.p7 | X:80688163 | AAAAGACGTTAAGTT[-/TTTGACGAAAGTCAAAAG]ACATTCAAAGTCATA | 254065 |
rs780569830 | in-del | -/TG | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80726212 | TACATGTTATATGTC[-/TG]TATAACATATAACAC | 254065 |
rs780570868 | snp | C/T | 2.2871e-05 | 0.00338156 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682588 | ATATTTTTGATATGA[C/T]TTTCAAATAAGGCAG | 254065 |
rs780572678 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674371 | TCACACAAATGTCAA[C/T]TCTTCTACATTTCAA | 254065 |
rs780595648 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80794198 | AAGAAATAAAAAAAA[-/T]AAAAATAAATAAAAT | 254065 |
rs780612693 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745797 | AAATTAAGTCATAAA[C/T]ATTAAGATGAGACAA | 254065 |
rs780616155 | snp | A/G | 2.31444e-05 | 0.00340171 | intron-variant | BRWD3 | GRCh38.p7 | X:80808608 | AATCAGCTGGGGGCC[A/G]GACGAAAAGAAAGGG | 254065 |
rs780623719 | snp | C/G | 2.59457e-05 | 0.00360169 | intron-variant | BRWD3 | GRCh38.p7 | X:80808488 | GGGGGTACAAGGTGG[C/G]GAGGGAGTGGTGAAA | 254065 |
rs780625403 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789821 | TGACCATGGAACTCC[-/T]TTTTTTTTTTTTTTC | 254065 |
rs780634783 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734397 | AAACTGTATCATTCA[A/T]CCAACAAAATCTACA | 254065 |
rs780639618 | snp | A/T | 2.56085e-05 | 0.00357821 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685520 | TCTGAGGATTCTCCC[A/T]CTTGCTCCTGATGAC | 254065 |
rs780652151 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80802439 | AGAGCAAGACTCTCA[A/T]CTTAAAAAAAAAAAA | 254065 |
rs780664489 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80696624 | CTTTATAATTCTAAA[A/C]CCTGTAGTAAAGAAT | 254065 |
rs780670624 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80778165 | AGTGCCTTGTTACCA[A/T]GTCTTTGGAAAATAG | 254065 |
rs780671069 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719391 | TAATAAAAAAGTTTT[G/T]ATTTATAAACGTAAA | 254065 |
rs780694245 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776950 | AAGTACTTCCCTCAT[C/T]CCTCTTATCCAGAGG | 254065 |
rs780696008 | snp | C/T | 0.000117664 | 0.00766929 | intron-variant | BRWD3 | GRCh38.p7 | X:80704873 | TCAAAATTATGGATA[C/T]CTAAGTATAGAAAAG | 254065 |
rs780700400 | snp | C/T | 2.30075e-05 | 0.00339164 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80728823 | TGTTCACTGCAGTAA[C/T]AACTGTGGTATCATA | 254065 |
rs780713038 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673990 | AAAGCAAAGTGTAAA[C/T]TGGGGGAAAAAAAAG | 254065 |
rs780715989 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80791646 | AAATGAAATGAAATA[A/C]AGAAAACAAAGATCA | 254065 |
rs780718832 | snp | C/T | 2.3731e-05 | 0.00344455 | intron-variant | BRWD3 | GRCh38.p7 | X:80725084 | TATAATAAAAATCAG[C/T]ATTAACAATGAAAGC | 254065 |
rs780722207 | in-del | -/TC | 4.26103e-05 | 0.00461555 | intron-variant | BRWD3 | GRCh38.p7 | X:80736105 | TTAAAAAAAAAAAAA[-/TC]TGATTCAAATAAAAA | 254065 |
rs780732114 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80722487 | GTTTAGCAGGAGGCA[C/T]ACATCATAGAGAGAA | 254065 |
rs780764232 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721385 | TAAATATGACATCAT[C/T]ACAGTAACTACAAGC | 254065 |
rs780782336 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701676 | AATACTAGGTCAGAA[C/T]TTCTAATAGCTAAAA | 254065 |
rs780786872 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770278 | CATCCTGATACCAAA[G/T]CCTGGCAGAGACACA | 254065 |
rs780795104 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80684279 | CATTGCTTTTCAATG[G/T]GCCAACTACCTCCCC | 254065 |
rs780795632 | snp | A/G | 2.3394e-05 | 0.00342001 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80729993 | AATTCTTGCCGTTCC[A/G]TCTCGACTTCCACTA | 254065 |
rs780802910 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802637 | TTAACAAAATGCATT[A/C]TTTCACATTTAACTC | 254065 |
rs780806949 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783674 | TTTGAAGTAACCTAA[A/G]TATCCAACACCAGAC | 254065 |
rs780835935 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738856 | AAGCAGAGTGAAAAA[A/G]GCAAACAAACACGCA | 254065 |
rs780850373 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675295 | CAGAAGAACCCTTTG[A/G]AATGATATGAGCAGA | 254065 |
rs780865406 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711412 | TCTGGCATAACATCA[C/T]ACAACAGAGAAAGAA | 254065 |
rs780871031 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80782613 | GATCAATAACCAGAA[A/T]ATAGCCAGGCACAGT | 254065 |
rs780875583 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789221 | CAATATAACTTAGGC[C/G]AATCAAATAACTTCT | 254065 |
rs780878249 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80695200 | TGCCTTCTGCCATGA[C/T]TGTAAATGTCCTAAG | 254065 |
rs780880886 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80761107 | GGTGATAAACCAAAG[A/G]AAAAAAAGACTCAAT | 254065 |
rs780883928 | snp | A/C | 4.58773e-05 | 0.00478921 | intron-variant | BRWD3 | GRCh38.p7 | X:80728913 | AATTATTGCTAAACA[A/C]AACAATTTGCAGTAT | 254065 |
rs780885519 | snp | A/C | 3.36078e-05 | 0.00409912 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809040 | GAGCTCCTGCACTAG[A/C]ACCTGAGCAAAAGGG | 254065 |
rs780893762 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791484 | ACATATAAAAATGTA[-/T]AACATCATTATAATT | 254065 |
rs780899338 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80769416 | CACAGTGCAATCAAA[C/T]TACAACTCAGGATTA | 254065 |
rs780915986 | snp | C/T | 4.67077e-05 | 0.00483236 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80684118 | TTCCAAAGTTTCTTT[C/T]ACAGTGCTGAAGTCC | 254065 |
rs780931430 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729636 | TTTTTAATGACCTAT[-/A]AAAAACTAAGGCAGA | 254065 |
rs780933254 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80763799 | TTTGACAGAGTAACA[C/T]GTCAATTCTCCCCAA | 254065 |
rs780935738 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734665 | CACTTAAGAATGGCT[A/G]AAATGATAAAATTTT | 254065 |
rs780952330 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714674 | TGAGGGCTGTGCCAC[A/G]GACCATTGGTCACTC | 254065 |
rs780973279 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80690540 | GCAAAGGCAGATTAA[C/G]CAGTCATGGAATACT | 254065 |
rs780973323 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80677590 | TGATGGCCATGAGGT[-/AA]TTAGGCAGAAGTTTT | 254065 |
rs781001197 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773056 | GTAACACAGATTAGT[A/G]ATTGACAAGATGGGG | 254065 |
rs781003767 | snp | A/G | 2.66937e-05 | 0.00365324 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80736006 | AACTTCATTGTTTTT[A/G]CATGCCATTGCCAGA | 254065 |
rs781010314 | snp | A/G | 2.29197e-05 | 0.00338517 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676960 | GCCTCCTCTTCCTCT[A/G]CCTCCTCTACTCCAT | 254065 |
rs781019232 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80738290 | AATAAAATCAGGTTA[C/T]GGATTGTTTAATAGA | 254065 |
rs781038769 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742803 | ATTTTGGGCTGAGAC[A/G]ATGGAGTTTTCTAAA | 254065 |
rs781046549 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804538 | CCACCACACCAGGCC[C/G]TGGTTCAGTCTTATG | 254065 |
rs781048328 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80691530 | CCTTACCAAGAAACC[A/C]ATCCAAAGTCAGGCT | 254065 |
rs781064952 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701088 | GGTTACTAAATGGAG[G/T]AATTTCAAGACAAAT | 254065 |
rs781071518 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80698292 | TATAGGGTCCTGCTT[A/C]AAGTTATATATTAGC | 254065 |
rs781091157 | snp | A/T | 2.35927e-05 | 0.0034345 | intron-variant | BRWD3 | GRCh38.p7 | X:80725071 | ATCATCATGTCCCTA[A/T]AATAAAAATCAGTAT | 254065 |
rs781107813 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80723527 | AAGGAATGTTTATAT[C/T]TTCATCACCCTATAA | 254065 |
rs781110823 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80724254 | CCATCCTAAAATTAA[A/C]GCACACAATCAATTT | 254065 |
rs781119019 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80808452 | CTAGAACCTCGTCGG[C/G]TGAGAGGTGGGGGGC | 254065 |
rs781124974 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673122 | GATAAATAACAGAAA[C/T]GTACTTAAAAGTATT | 254065 |
rs781128354 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80754184 | TGTTTGTGTCATCTA[C/T]AATTTCCTAAGTGTT | 254065 |
rs781141288 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80741965 | ATTGCTTTTGGTGTT[C/T]TAGACATGAAGTCCT | 254065 |
rs781152524 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697850 | GTAATGGAATTTGGG[G/T]AGTTCTACTTTAAGT | 254065 |
rs781182419 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728358 | AGACCTTTCTTTTCC[-/T]ACTTCTTCCTCTTAC | 254065 |
rs781182458 | snp | C/T | 7.58255e-05 | 0.00615687 | intron-variant | BRWD3 | GRCh38.p7 | X:80687037 | TTATATCTAAAAGAT[C/T]TTTCCTTAACTCAGT | 254065 |
rs781184125 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80773896 | AATCACATTCTGGCA[C/T]CTGCCTAACCTTCTC | 254065 |
rs781199393 | in-del | -/GAAAGAAAGAAAGAAAG | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80730412 | AAAGAAAGAAAGAAA[-/GAAAGAAAGAAAGAAAG]GAAAGAAAGAAAGAA | 254065 |
rs781223651 | in-del | -/TT | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80728441 | CTACCCCTATAACGG[-/TT]TAACAATGAAAAAAT | 254065 |
rs781226770 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722264 | AAGCTTTTACTACAA[C/T]TCCATACTATAGAAA | 254065 |
rs781234285 | in-del | -/TTTG | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669271 | ACCTTCAACTACTGT[-/TTTG]TTTTAGTAACTTCTT | 254065 |
rs781258661 | snp | C/T | 2.44185e-05 | 0.00349409 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695940 | TCTTTGGCTTCATTA[C/T]AAAACTGATGTAGCA | 254065 |
rs781260793 | snp | G/T | 2.2872e-05 | 0.00338164 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80719535 | TAAATGTGGAACATC[G/T]CCTTCATTAATTAGT | 254065 |
rs781268702 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80747625 | ATTTCTTTCATCAAT[A/G]TTTTATAGTTTTCAC | 254065 |
rs781270884 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766693 | AGCTCCCAGCGTGAT[C/T]GATGCAGAAGATGGG | 254065 |
rs781281887 | snp | C/T | 2.29347e-05 | 0.00338627 | missense, downstream-variant-500B, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80704751 | TCATCAGAGCTGCTG[C/T]ATATTTTACGTGTTG | 254065 |
rs781283753 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781387 | TACCTGATTGGTCAC[A/G]TGTGAGCTAAGTTGC | 254065 |
rs781290993 | in-del | -/ACATAATGAATTAGG | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80680333 | GTCCAAGATAGACGC[-/ACATAATGAATTAGG]TCAGTGTTTCTTTTT | 254065 |
rs781291452 | snp | C/T | 0.000121606 | 0.00779669 | intron-variant | BRWD3 | GRCh38.p7 | X:80703625 | CGAAAAGTATATGTA[C/T]AAAACACAGTTCTCC | 254065 |
rs781313060 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80805660 | CCTACCCCAGGCCGG[G/T]CGCGGTGGCTCATGC | 254065 |
rs781321468 | snp | A/G | 0.000479573 | 0.0154776 | intron-variant | BRWD3 | GRCh38.p7 | X:80809317 | GCTCTGGGGAAGAGG[A/G]GGGAAAAGAGGTTCA | 254065 |
rs781353489 | in-del | -/AA | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678563 | GCGGAAATTTTCAGT[-/AA]AGAGATAATATTTAG | 254065 |
rs781355799 | in-del | -/AACTC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80795029 | TACTATGCTTTAAAT[-/AACTC]AGCTATGTAGCCAAA | 254065 |
rs781359385 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688588 | CTCTAAGGGATAATT[C/T]TTTAATATGAAGAGT | 254065 |
rs781378262 | snp | C/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80725958 | TACATGTCTATATAA[C/G]ACATAACATGTTTAC | 254065 |
rs781381085 | in-del | -/TT | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80790392 | TGAATTCTAAATAAC[-/TT]AAACTTAAGCATCTT | 254065 |
rs781385256 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758772 | CCTGGGCAATATAGC[A/G]AGATCCCATCTTTAA | 254065 |
rs781385801 | snp | A/C | 2.90213e-05 | 0.00380917 | intron-variant | BRWD3 | GRCh38.p7 | X:80689751 | CTCATTCCTACTAAT[A/C]ATGCTGTGATTCTTA | 254065 |
rs781404615 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80770765 | AGGGCAATCAGGCAA[C/G]AGAAAGAAATAAAGG | 254065 |
rs781435295 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80766117 | AAAGCAGATTGCCCT[C/T]CCCAATGAATCCGGT | 254065 |
rs781435400 | in-del | -/AC | 0.0199612 | 0.0978884 | intron-variant | BRWD3 | GRCh38.p7 | X:80795352 | ATTGTGTATATATAT[-/AC]ACACACACACACACA | 254065 |
rs781438726 | in-del | -/ACA | 2.87778e-05 | 0.00379316 | intron-variant | BRWD3 | GRCh38.p7 | X:80685569 | TATACTGGTTTCCAG[-/ACA]ACAACTATAACAAAA | 254065 |
rs781440559 | snp | A/C | 0.0419931 | 0.138684 | intron-variant | BRWD3 | GRCh38.p7 | X:80712906 | AGTGAGGAGCCCCTC[A/C]GCCCGGCAGCCGCCC | 254065 |
rs781445666 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776474 | CAAAATGTTATATAT[C/T]GACCACTGCTTTTGA | 254065 |
rs781447899 | snp | A/T | 2.1166e-05 | 0.00325309 | intron-variant | BRWD3 | GRCh38.p7 | X:80691992 | AGCTAGGTATAAGAT[A/T]AAAAAAAAAAAATTA | 254065 |
rs781449424 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80687689 | TACCTGATTTCCTTC[C/T]GGGAATCTGGAATCT | 254065 |
rs781458534 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748131 | TACAGGCATGAGCCA[C/T]CATGCCCAGCCGAGA | 254065 |
rs781467205 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782408 | CCTATGAAACCACTA[A/G]AAGAAAACATCGGTG | 254065 |
rs781487765 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687987 | CCTTCTAGCAATTCT[C/T]CAAATATGGGGTTGG | 254065 |
rs781516941 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679340 | CTGTGAGATTTTAAG[C/T]TGGGTGGCAAGAAAG | 254065 |
rs781522162 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80711738 | TTAGACAATAACTCT[G/T]TCAACTAATTGCTAA | 254065 |
rs781570218 | snp | A/G | 2.2887e-05 | 0.00338274 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682002 | ACATATTTACCAGGA[A/G]ATGAGAAAGGAGAGC | 254065 |
rs781578060 | snp | C/T | 2.29518e-05 | 0.00338753 | intron-variant | BRWD3 | GRCh38.p7 | X:80716263 | ACCCTAATAACAAGT[C/T]AAAGGTCAAAGTAAC | 254065 |
rs781582382 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764310 | ATGGGGCTAGGCAAA[G/T]AATTTTTTTTTTAGA | 254065 |
rs781614846 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80749271 | GTTGAAAGTGAGGTA[C/T]TGATGTCTCCTATTA | 254065 |
rs781640071 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807127 | TAGTAGGCACTGTTG[C/T]TTTTGCCTCTTTTAG | 254065 |
rs781669433 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80764840 | GAAATTAAAAATAAT[A/C]TAATTAAAAATGGGC | 254065 |
rs781678181 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745072 | CTCAAAAGCATACAG[C/T]ATTATCTGCTTAATA | 254065 |
rs781681858 | snp | A/G | 2.38163e-05 | 0.00345074 | intron-variant | BRWD3 | GRCh38.p7 | X:80692163 | CAGCTATTAAAAAAT[A/G]AGAAGATGCAAATCA | 254065 |
rs781688495 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704599 | TTAGAGAAAAGTCAA[C/T]GTTACAATTAAATAT | 254065 |
rs781690599 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693597 | AACTTATTGGGAACT[A/C]GAGTAAAGGTCACTC | 254065 |
rs781699839 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802827 | AATGTCAAGCAGGCC[-/A]AGGTGCGGTGGCTCA | 254065 |
rs781727571 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741138 | TTGTTCAATTCCCAC[C/T]TATGAGTGAGAACAT | 254065 |
rs781736002 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80754484 | TCCTCTTTTCCAATT[C/T]GGATGCCTTTTATTT | 254065 |
rs781748393 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774370 | TTGAGCTCCAGAGAT[C/G]TTACCTCAGCTTCCC | 254065 |
rs781751446 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726547 | AAGCATAGAGAACAT[C/G]CTGAAGCTGCACTTA | 254065 |
rs781754475 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80777096 | AAAATGCATTTTGAA[C/T]TATCCTACAGATTCA | 254065 |
rs781778590 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80786936 | GTCTTTATTTGCAGA[C/T]AACAGGGTTATCTAT | 254065 |
rs781779498 | snp | C/T | 4.30182e-05 | 0.00463759 | intron-variant | BRWD3 | GRCh38.p7 | X:80745740 | ATTCACTGAAAAAAA[C/T]ACGAAATTAACTTAA | 254065 |
rs796193857 | snp | A/C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712915 | CCCCTCCGCCCGGCA[A/C/G]CCGCCCCGTCTGAGA | 254065 |
rs796200708 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80758300 | CACTTATCCAATTTC[A/T]GGAATGAGTAAAATA | 254065 |
rs796336227 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80689003 | AAAAAATAAAAAAAA[-/A]CAGCATTGGAGATTT | 254065 |
rs796347586 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695415 | ATGTTCTGTATTGTA[G/T]TGTTATACAATAGAG | 254065 |
rs796373707 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80751821 | ATGAGAAAATGTGAT[A/G]TTTGACTTTCTGTAC | 254065 |
rs796453486 | in-del | -/AC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750892 | CACACACACACACAC[-/AC]GCAAAAATCATTAAG | 254065 |
rs796493053 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740440 | AGAAGCCAACGTATT[C/T]CACATTAAAAATCAA | 254065 |
rs796537547 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782932 | AAATAACCAGAATGT[A/T]AAAGGAGCTCAAACA | 254065 |
rs796538451 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80786517 | CCCTTTTAATTTGCC[-/TA]TATATATATATATAT | 254065 |
rs796567773 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712901 | TGAGAAGTGAGGAGC[C/T]CCTCCGCCCGGCAGC | 254065 |
rs796658772 | in-del | -/CG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750893 | ACACACACACACACA[-/CG]CAAAAATCATTAAGT | 254065 |
rs796718643 | in-del | -/GT | | | utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809711 | AGAGGGAGAGAGAGA[-/GT]GAGTGAGTGAGAGAG | 254065 |
rs796748495 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80740583 | AATCCCTGTCTCTAC[-/A]AAAAAAAATACAAAA | 254065 |
rs796959019 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685949 | GAATAGATACACTCC[C/T]AGGAAAGAAATCCTA | 254065 |
rs796967741 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783402 | AAAAAAAAAAAAAAA[-/A]TCCAAAAGACATGCA | 254065 |
rs796975494 | in-del | -/ACAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750890 | CACACACACACACAC[-/ACAC]GCAAAAATCATTAAG | 254065 |
rs796990134 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750936 | AAGAAATTGGAAATT[A/C]TGCCATTCACAACAA | 254065 |
rs797015165 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715224 | TCTTAAAAAAAAAAA[-/AA]CTTACCAGAGAACAG | 254065 |
rs797045416 | snp | G/T | | | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722683 | TCCTCACCTCATGCC[G/T]CCTCCATTTTTGGTG | 254065 |
rs797045417 | snp | A/G | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717699 | GGCTTCGAAGACATA[A/G]TAGTCAAATTGAAGG | 254065 |
rs797045418 | snp | A/G | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691114 | CCCTTGTATTGTACT[A/G]TAGTTGCTTATCCAA | 254065 |
rs797045419 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80690005 | TCCTATAGTTAAAGC[A/G]GCTAAAATTGTAACT | 254065 |
rs863224851 | snp | G/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682607 | AGCATGATGCTGCGA[G/T]TATCTGCCTTATTTG | 254065 |