SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1398468 | snp | A/C | 0.0510748 | 0.151422 | intron-variant | BRWD3 | GRCh38.p7 | X:80678717 | aCCAGCCAGTGGGGT[A/C]GGTAGGAAACAAGAG | 254065 |
rs2063579 | snp | A/G | 0.499113 | 0.0210409 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80669747 | GAATTGCAACATGAC[A/G]AAAATCAACCACAAA | 254065 |
rs2089956 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80694675 | aaaatttgactgccc[C/T]gctggattttagact | 254065 |
rs2137444 | snp | C/T | 0.499628 | 0.0136373 | intron-variant | BRWD3 | GRCh38.p7 | X:80734682 | TGAAATATACAGAAC[C/T]TAAAATTTTATCATT | 254065 |
rs2203205 | snp | A/G | 0.463138 | 0.130661 | intron-variant | BRWD3 | GRCh38.p7 | X:80753384 | tactcaggaggctga[A/G]gcaggaggattgctt | 254065 |
rs2683778 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770361 | tggattcagtttgcc[A/C]gtattttgttgagga | 254065 |
rs3029738 | in-del | -/TATA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687101 | CTATCTGTATGTGTG[-/TATA]TATATATATATATAT | 254065 |
rs3106406 | snp | A/G | 0.499242 | 0.0194554 | intron-variant | BRWD3 | GRCh38.p7 | X:80729613 | GGTAGAAAGTAAAAT[A/G]GATATATTTTTTAAT | 254065 |
rs3106407 | snp | A/G | 0.499135 | 0.0207767 | intron-variant | BRWD3 | GRCh38.p7 | X:80738966 | tgctcaggaccatca[A/G]tagcttccaatctca | 254065 |
rs3122406 | snp | A/G | 0.477601 | 0.10343 | intron-variant | BRWD3 | GRCh38.p7 | X:80681585 | TGAAACCATATCTCT[A/G]TTATTTTATTCTAAC | 254065 |
rs3122407 | snp | C/T | 0.00557619 | 0.0525071 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80688070 | ACTTATTTACTCACC[C/T]TTCTTCCAGATGAAG | 254065 |
rs3123256 | snp | A/C | 0.0510748 | 0.151422 | intron-variant | BRWD3 | GRCh38.p7 | X:80759981 | TAACATGCACTGCTA[A/C]TCCTCACCTTCCAAT | 254065 |
rs3123257 | snp | C/T | 0.499179 | 0.0202482 | intron-variant | BRWD3 | GRCh38.p7 | X:80780566 | TCCATCTATTTAATA[C/T]TTAGTGAGCACTTAC | 254065 |
rs3123258 | snp | A/G/T | 0.0214859 | 0.101397 | intron-variant | BRWD3 | GRCh38.p7 | X:80781385 | actacctgattggtc[A/G/T]cgtgtgagctaagtt | 254065 |
rs3123259 | snp | A/G | 0.461978 | 0.132535 | intron-variant | BRWD3 | GRCh38.p7 | X:80782420 | ctaaaagaaaacatc[A/G]gtgaaactctccagg | 254065 |
rs3123260 | snp | A/G | 0.499709 | 0.0120495 | intron-variant | BRWD3 | GRCh38.p7 | X:80783267 | tagtgcacacctgta[A/G]tcccagctactagga | 254065 |
rs3123261 | snp | A/G | 0.0287145 | 0.11633 | intron-variant | BRWD3 | GRCh38.p7 | X:80787278 | caatgctgtcaagat[A/G]tcagttattctaaaa | 254065 |
rs3123262 | snp | A/T | 0.381599 | 0.21256 | intron-variant | BRWD3 | GRCh38.p7 | X:80794190 | CTCAAAAAAAGAAAT[A/T]AAAAAAATAAAAATA | 254065 |
rs3123263 | snp | A/G | 0.0199298 | 0.0978146 | intron-variant | BRWD3 | GRCh38.p7 | X:80794385 | GTGGCTGCACCTCTA[A/G]TCTCAGCTATTCGGG | 254065 |
rs3132151 | snp | A/C | 0.0510748 | 0.151422 | intron-variant | BRWD3 | GRCh38.p7 | X:80767495 | aaaactaacaaacaa[A/C]aaggaatagcatcaa | 254065 |
rs3132152 | snp | C/G | 0.0520783 | 0.152732 | intron-variant | BRWD3 | GRCh38.p7 | X:80770553 | acaaaattcaacaac[C/G]cttcatgctaaaaac | 254065 |
rs3132153 | snp | C/T | 0.499709 | 0.0120495 | intron-variant | BRWD3 | GRCh38.p7 | X:80785946 | GACGCAGGAGAATCA[C/T]TTGAACCCAGAAGCG | 254065 |
rs3132154 | snp | C/T | 0.499628 | 0.0136373 | intron-variant | BRWD3 | GRCh38.p7 | X:80795240 | AGAAAAACCAGAATA[C/T]TAAAAACCTTTAGAT | 254065 |
rs3132155 | snp | C/T | 0.499179 | 0.0202482 | intron-variant | BRWD3 | GRCh38.p7 | X:80796144 | TTTTGTTTTTTTTTT[C/T]TTTTGAGTCGGAGTC | 254065 |
rs3132156 | snp | A/G | 0.4992 | 0.019984 | intron-variant | BRWD3 | GRCh38.p7 | X:80796896 | AAATACTTCATGGCT[A/G]GGAACGGTGGCTCAT | 254065 |
rs3132157 | snp | A/G | 0.499628 | 0.0136373 | intron-variant | BRWD3 | GRCh38.p7 | X:80797862 | GCACTTTGGGAGGCC[A/G]AGGCGGATGGATCAC | 254065 |
rs3132158 | snp | C/T | 0.0199298 | 0.0978146 | intron-variant | BRWD3 | GRCh38.p7 | X:80797955 | AAAAAATTAGCTGGG[C/T]CTGGTTGTAAGCGCC | 254065 |
rs3132159 | snp | A/G | 0.0515767 | 0.15208 | intron-variant | BRWD3 | GRCh38.p7 | X:80800465 | GGATTGATTGAGCCC[A/G]GGAGGTGGAGGCTGC | 254065 |
rs3132160 | snp | G/T | 0.368086 | 0.220354 | intron-variant | BRWD3 | GRCh38.p7 | X:80803975 | ACTTTTAAACTTGAA[G/T]GTGTTATATGCAGAT | 254065 |
rs3132165 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687039 | ATATCTAAAAGATCT[C/T]TCCTTAACTCAGTTG | 254065 |
rs3132166 | snp | A/G | 0.499221 | 0.0197197 | intron-variant | BRWD3 | GRCh38.p7 | X:80693594 | AGGAACTTATTGGGA[A/G]CTAGAGTAAAGGTCA | 254065 |
rs3132167 | snp | C/T | 0.499242 | 0.0194554 | intron-variant | BRWD3 | GRCh38.p7 | X:80694290 | ggatgtatggaaatg[C/T]ctggatatccaggca | 254065 |
rs3132168 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712294 | cctgtgattgcaggc[A/G]cgcgccgccacacct | 254065 |
rs3132169 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725752 | ACATGCCTATATAAC[A/G]TATAACATGTTTACA | 254065 |
rs3132170 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80725876 | ATAACATGTTTACAT[A/G]TGTTACATGCCTATA | 254065 |
rs3132171 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725923 | GTTACATGCCTATAT[C/G]ACATAACTTGTTTAC | 254065 |
rs3132172 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725931 | CCTATATGACATAAC[A/T]TGTTTACATGTTACA | 254065 |
rs3132173 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725945 | CTTGTTTACATGTTA[C/T]ATGTCTATATAACAC | 254065 |
rs3132174 | snp | A/C | 0.499179 | 0.0202482 | intron-variant | BRWD3 | GRCh38.p7 | X:80732955 | CCATCCTGGTGAAAC[A/C]CCGTCTCTACTAAAA | 254065 |
rs3132175 | snp | A/G | 0.0287145 | 0.11633 | intron-variant | BRWD3 | GRCh38.p7 | X:80733057 | ATCGCTTGAACCCAG[A/G]AGATGGAGGTTGCAG | 254065 |
rs3132176 | snp | G/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80751240 | tcaaaattgctaaaa[G/T]aatagatttgtaatg | 254065 |
rs3132178 | snp | A/C | 0.499656 | 0.0131081 | intron-variant | BRWD3 | GRCh38.p7 | X:80758753 | aatagccactgcact[A/C]catcctgggcaatat | 254065 |
rs3810676 | snp | A/G | 0.256019 | 0.249928 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673778 | TATATGCTCTCACGG[A/G]CCTAAATATAACAGT | 254065 |
rs3835169 | in-del | -/TGTG | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676340 | tgtgtttcgtgtgtg[-/TGTG]tctgtgtgtgtgtat | 254065 |
rs3923574 | snp | C/T | 0.4992 | 0.019984 | intron-variant | BRWD3 | GRCh38.p7 | X:80744803 | ATCTATTTATTAAAA[C/T]ATAGCATTCATCATC | 254065 |
rs4240018 | snp | C/G | 0.500016 | 0.00303941 | intron-variant | BRWD3 | GRCh38.p7 | X:80733519 | ATGAAACAGATTTTT[C/G]GTTAAAATGGACTTA | 254065 |
rs4436262 | snp | C/T | 0.102711 | 0.202005 | intron-variant | BRWD3 | GRCh38.p7 | X:80769263 | gacatctacagaact[C/T]tccaccccaaatcaa | 254065 |
rs4567187 | snp | C/T | 0.49816 | 0.0302753 | intron-variant | BRWD3 | GRCh38.p7 | X:80802668 | ACTTGTTCCCCACAA[C/T]AAATGGGAAATTTTC | 254065 |
rs4609320 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80699620 | ATACCAAAGCTGTCA[A/G]AACCTTGAGAGTGTT | 254065 |
rs4625156 | snp | C/T | 0.448034 | 0.152586 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792641 | TTACACAACTATTTA[C/T]CTTGGAGAATTAGGA | 254065 |
rs4826025 | snp | A/G | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80705949 | ctttacaaacactac[A/G]cttaggttacactga | 254065 |
rs4826026 | snp | A/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80765911 | gattaTTTATTTATT[A/T]AAGTATTAAATACTT | 254065 |
rs4826027 | snp | C/T | 0.0709308 | 0.174454 | intron-variant | BRWD3 | GRCh38.p7 | X:80766129 | cctccccaatgaatc[C/T]ggtgggctttattca | 254065 |
rs4826028 | snp | A/G | 0.169532 | 0.236696 | intron-variant | BRWD3 | GRCh38.p7 | X:80789746 | CATATGAAAAGCTAC[A/G]AAAAGTACACCATTC | 254065 |
rs4826191 | snp | C/T | 0.0728917 | 0.176444 | intron-variant | BRWD3 | GRCh38.p7 | X:80763254 | ttagctattaagtgg[C/T]agtcaagattcaaac | 254065 |
rs4826192 | snp | A/G | 0.445616 | 0.155675 | intron-variant | BRWD3 | GRCh38.p7 | X:80787639 | ttaaaatgatcaaaa[A/G]tctaaatatacaaca | 254065 |
rs5902802 | in-del | -/ATAT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687112 | TGTGTATATATATAT[-/ATAT]ATATATATGGCAGCT | 254065 |
rs5902803 | in-del | -/A | 0.499628 | 0.0136373 | intron-variant | BRWD3 | GRCh38.p7 | X:80698708 | TTAAAAAAAAAAAAA[-/A]GAGTAAGAAATCACA | 254065 |
rs5902804 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714747 | ATTCTTCGTCAAAGG[-/G]CACATAGACGCACAC | 254065 |
rs5913312 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676341 | GTGTTTCGTGTGTGT[C/G]TGTCTGTGTGTGTGT | 254065 |
rs5913313 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676345 | TTCGTGTGTGTGTGT[C/G]TGTGTGTGTGTATGT | 254065 |
rs5913315 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739283 | gttgaaagcatggta[C/T]tgccatttgtttgga | 254065 |
rs5913317 | snp | A/G | 0.0831127 | 0.186141 | intron-variant | BRWD3 | GRCh38.p7 | X:80757308 | ACAGGGCAATCAATC[A/G]ACATAATTTTAGCCA | 254065 |
rs5913319 | snp | C/T | 0.0505727 | 0.150761 | intron-variant | BRWD3 | GRCh38.p7 | X:80771593 | caccaaaagcaatgg[C/T]aacaaaagccaaaat | 254065 |
rs5913320 | snp | A/T | 0.0535814 | 0.15466 | intron-variant | BRWD3 | GRCh38.p7 | X:80780351 | ACTTTTTTCATTATA[A/T]TTTATATAATAAAAT | 254065 |
rs5959727 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80706235 | tgtctcagcctccca[A/G]gtagctgggattaca | 254065 |
rs5959728 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80721332 | TTTCAAGTTTATCTC[C/T]CATTTAATTAATATT | 254065 |
rs6524017 | snp | A/G | 0.0835963 | 0.186574 | intron-variant | BRWD3 | GRCh38.p7 | X:80678612 | gagctcactgagtga[A/G]taagtaaagagagac | 254065 |
rs6524018 | snp | A/G | 0.0445249 | 0.142408 | intron-variant | BRWD3 | GRCh38.p7 | X:80699202 | cctgggcaacagagc[A/G]agactccgtTGCAaa | 254065 |
rs6616696 | snp | A/C | 0.00896606 | 0.0663524 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669012 | TTTTTTAAGTCATTT[A/C]TTATCACTAATATGA | 254065 |
rs6616697 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | BRWD3 | GRCh38.p7 | X:80710842 | TGTGAGTTTTTTCTA[A/G]GCAACCTCACTAAAA | 254065 |
rs6616698 | snp | C/G/T | 0.0911644 | 0.194338 | intron-variant | BRWD3 | GRCh38.p7 | X:80713500 | GAAGGCAGCATGCTC[C/G/T]TTAAGAGTCATCACC | 254065 |
rs6616699 | snp | A/C | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80733084 | gcagtgagccaagat[A/C]gcaccaccgcactcc | 254065 |
rs6616700 | snp | A/T | 0.18863 | 0.24235 | intron-variant | BRWD3 | GRCh38.p7 | X:80743847 | TTTTAGTTATTTATT[A/T]AAAAAGATAATCATA | 254065 |
rs6616701 | snp | A/G | 0.0772873 | 0.180749 | intron-variant | BRWD3 | GRCh38.p7 | X:80773882 | AAGTCCTGTACTACA[A/G]TCACATTCTGGCATC | 254065 |
rs6616703 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80782791 | tgcttatagttccag[C/T]taatcaggaagccga | 254065 |
rs6622355 | snp | A/G | 0.193212 | 0.243465 | intron-variant | BRWD3 | GRCh38.p7 | X:80695520 | AGTAAAGAAAGAAGG[A/G]TAAAAGAGCAAAAGA | 254065 |
rs6622356 | snp | A/T | 0.204314 | 0.24579 | intron-variant | BRWD3 | GRCh38.p7 | X:80697714 | ttctttatccagtcc[A/T]ccactgacgggcatc | 254065 |
rs6622357 | snp | A/G | 0.0425 | 0.139441 | intron-variant | BRWD3 | GRCh38.p7 | X:80708841 | aaaagaaTTGGGAAT[A/G]GCACAAGAATGAGAG | 254065 |
rs6622358 | snp | A/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80712136 | TCCAGGAGAGAGTTG[A/T]TTAAAATAAAAATGA | 254065 |
rs6622359 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712396 | tcgcgagtgatccgc[A/C]agcctcggcctcccg | 254065 |
rs6622360 | snp | G/T | 0.203907 | 0.245714 | intron-variant | BRWD3 | GRCh38.p7 | X:80712590 | tctgggaagtgagga[G/T]cgtctctgcctggct | 254065 |
rs6622361 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80733943 | GGTAATCTTCTTTTA[A/G]AATAATTAACCCATA | 254065 |
rs6622362 | snp | A/G | 0.204314 | 0.24579 | intron-variant | BRWD3 | GRCh38.p7 | X:80740842 | ACACATACTAACTCT[A/G]ACTGGCAAACATCTT | 254065 |
rs6622363 | snp | C/T | 0.000850656 | 0.0206059 | intron-variant | BRWD3 | GRCh38.p7 | X:80745751 | AAAATACGAAATTAA[C/T]TTAAAACTTAAAAGT | 254065 |
rs6622364 | snp | C/T | 0.210394 | 0.246843 | intron-variant | BRWD3 | GRCh38.p7 | X:80777533 | AAGTAGCTGGGACTA[C/T]AGGCACACAGCACCA | 254065 |
rs6622365 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781216 | cagagctcccataaa[A/T]tgggaggggacccaa | 254065 |
rs6622366 | snp | C/T | 0.0142023 | 0.083063 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792453 | GTAACTGGTTATAAA[C/T]AGCTGTGTTTTTTTC | 254065 |
rs6622367 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793260 | AATTTTGATTTACCT[A/G/T]TTACGAAAAGTACAA | 254065 |
rs6622368 | snp | A/G | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80797417 | CCCTAGAAATACAAC[A/G]CATTTAGCATATACA | 254065 |
rs6652413 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701435 | cgcctgtaatcccag[C/T]tactccagagactga | 254065 |
rs6652975 | snp | A/G | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80804860 | AACTAGGAAGCAGAA[A/G]ATAAAGTGCCCAGAT | 254065 |
rs7049509 | snp | A/T | 0.447863 | 0.152807 | intron-variant | BRWD3 | GRCh38.p7 | X:80695730 | GGTTTAGAGATTATA[A/T]GCCACACACAATGTG | 254065 |
rs7050680 | snp | G/T | 0.0570788 | 0.159001 | intron-variant | BRWD3 | GRCh38.p7 | X:80805826 | tgtagtcccagctac[G/T]tgggaggctgaagca | 254065 |
rs7051304 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80781079 | CAAGGGTCCTGAGCT[A/G]TATACAGTGTAAATT | 254065 |
rs7051376 | snp | C/G | 0.233695 | 0.249468 | intron-variant | BRWD3 | GRCh38.p7 | X:80808766 | ACAAGTATATGGGGG[C/G]GGGGGGGAAGGGGGG | 254065 |
rs7051605 | snp | C/G | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80750449 | tcaaaagacgacata[C/G]aaatggccaatggat | 254065 |
rs7051637 | snp | A/G | 0.0724019 | 0.175951 | intron-variant | BRWD3 | GRCh38.p7 | X:80781304 | cgtgtgctctcaggc[A/G]atagatgagtggcta | 254065 |
rs7052331 | snp | C/T | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80758153 | gtggtgagccaagat[C/T]gcgccattgcactcc | 254065 |
rs7054751 | snp | C/T | 0.344237 | 0.231559 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793499 | CTAAGAAAACAAAAA[C/T]AACATTGGCAAGATA | 254065 |
rs7056097 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676020 | GTAGTATAAATATAT[A/C]CTTCAGTTCAGTACA | 254065 |
rs7056176 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80757767 | AATAGATTTACTGTA[C/T]ATATTTTACAAATTT | 254065 |
rs7059257 | snp | A/T | 0.447692 | 0.153029 | intron-variant | BRWD3 | GRCh38.p7 | X:80738324 | GTTTTAAATGAGAAA[A/T]CATGTTATGGACTGT | 254065 |
rs7061262 | snp | A/G | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80782830 | gctcactaggagttc[A/G]tggctgcagtgagct | 254065 |
rs7061967 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801452 | tgaactcctgacctc[A/G]tgatccacccaccta | 254065 |
rs7063880 | snp | G/T | 0.204314 | 0.24579 | intron-variant | BRWD3 | GRCh38.p7 | X:80806266 | TATAAAAACAGAAAA[G/T]AATATTTAAAAGATA | 254065 |
rs7065162 | snp | A/C | 0 | 0 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670432 | CTTTTTCTTGACCTT[A/C]TCAACTTGGAAAAAA | 254065 |
rs7065208 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735448 | ACCATTATGAGAAAT[C/G]TTCTTACCAAAGTAA | 254065 |
rs7065450 | snp | C/G | 0.348057 | 0.229967 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670616 | GTAGATACGGTGTCT[C/G]ACTATGCTGCCCAGG | 254065 |
rs7065593 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80765501 | acTTTACTTTACTTT[A/G]CTATTCtgggtagta | 254065 |
rs7066585 | snp | G/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80784079 | ctaaaaatataattg[G/T]aatgtctgtataaca | 254065 |
rs7066695 | snp | C/T | 0.115825 | 0.210943 | intron-variant | BRWD3 | GRCh38.p7 | X:80802612 | AATTCATTTGCACAG[C/T]ATTTTACAATTAACA | 254065 |
rs7317407 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770216 | aaactattccaatca[A/G]taggaaaaaagggaa | 254065 |
rs7358014 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80723590 | TAAGGTTCTGGCAGT[A/G]CAGATCACAATTGAG | 254065 |
rs7392261 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80770657 | atcatactgaatggg[C/T]aaaaactggaggcac | 254065 |
rs7886875 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80712785 | gggatgtgaggagca[C/T]ctctgcccggccgcg | 254065 |
rs9713445 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770179 | GAATGGTACCAGTTC[C/T]TCCTTGTACCTCTGG | 254065 |
rs10041938 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770010 | atctagaagaaatgg[C/T]taaattccctgacac | 254065 |
rs10465446 | snp | A/G | 0.0835963 | 0.186574 | intron-variant | BRWD3 | GRCh38.p7 | X:80771151 | gaatacgaagaatca[A/G]tatcgtgaaaatggc | 254065 |
rs10573264 | in-del | -/AAC | 0.204314 | 0.24579 | intron-variant | BRWD3 | GRCh38.p7 | X:80735839 | ATCCTAAAATCTCTT[-/AAC]AACCTATTGAAGTAG | 254065 |
rs10645949 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726008 | ATAACATGTTTACAT[-/AT]GTTATATGTCTATAT | 254065 |
rs10645950 | in-del | -/AT/ATAT | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80726077 | ACATGTTTACATGTT[-/AT/ATAT]GTCTGTATAACAACA | 254065 |
rs10645951 | in-del | -/GT/TG | 0.499262 | 0.0191911 | intron-variant | BRWD3 | GRCh38.p7 | X:80726376 | TGTTTACATGTTATA[-/GT/TG]TCTGTATAACATAAC | 254065 |
rs10683328 | in-del | -/GT | 0.479788 | 0.0984769 | intron-variant | BRWD3 | GRCh38.p7 | X:80725825 | ACATGCCTATATAAC[-/GT]ATAACATGTTTACAT | 254065 |
rs10683329 | in-del | -/AT | 0.499302 | 0.0186625 | intron-variant | BRWD3 | GRCh38.p7 | X:80726006 | ACATAACATGTTTAC[-/AT]ATGTTATATGTCTAT | 254065 |
rs10683330 | in-del | -/AT/TA/TATA | 0.450162 | 0.155017 | intron-variant | BRWD3 | GRCh38.p7 | X:80726076 | AACATGTTTACATGT[-/AT/TA/TATA]TGTCTGTATAACAAC | 254065 |
rs10711199 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790218 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 254065 |
rs11266586 | snp | C/G | 0.373824 | 0.217181 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670278 | AAAGCAACTGTAAGC[C/G]TATAGGCTTAACTAT | 254065 |
rs11312634 | in-del | -/T | 0.458015 | 0.138671 | intron-variant | BRWD3 | GRCh38.p7 | X:80719061 | CTTGTCTTCAGTGTA[-/T]TTTTTTTTTTTATTC | 254065 |
rs11332158 | in-del | -/A | 0.499262 | 0.0191911 | intron-variant | BRWD3 | GRCh38.p7 | X:80747507 | TACCAATAGAAGGGG[-/A]AAAAAAAAACAAAAC | 254065 |
rs11390755 | in-del | -/A/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80715213 | AATCTCTTAAAAAAA[-/A/AA]AAAAAACTTACCAGA | 254065 |
rs11546185 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710543 | GACTACAAAGAATGT[C/T]TCCATTGGAATTGTT | 254065 |
rs11721766 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770148 | TAGAATTTGGCTGCA[A/T]ATCCATCTGGTCCTG | 254065 |
rs11796018 | snp | C/T | 0.447863 | 0.152807 | intron-variant | BRWD3 | GRCh38.p7 | X:80737124 | AATATTATTCATTAA[C/T]AACTGATGTGCAGTA | 254065 |
rs11797410 | snp | A/G | 0.343052 | 0.232037 | intron-variant | BRWD3 | GRCh38.p7 | X:80798082 | ACTAGGCGACAGAGC[A/G]AGACTCCACCTCAAA | 254065 |
rs11797881 | snp | A/C | 0.348349 | 0.229842 | intron-variant | BRWD3 | GRCh38.p7 | X:80730172 | TGGCAGTTCTTCAAA[A/C]TGTTAAACATAGAGT | 254065 |
rs11798758 | snp | C/T | 0.447521 | 0.15325 | intron-variant | BRWD3 | GRCh38.p7 | X:80753018 | ttcttttgaaaaata[C/T]ctatttatgtcttta | 254065 |
rs12007767 | snp | C/G | 0.00791544 | 0.0624105 | intron-variant | BRWD3 | GRCh38.p7 | X:80795121 | ACCATATATAGATAA[C/G]AATGAAACTATAAAA | 254065 |
rs12009486 | snp | C/T | 0.0183711 | 0.0940641 | intron-variant | BRWD3 | GRCh38.p7 | X:80789398 | ttcttttttttgaga[C/T]ggagtctcgctctgt | 254065 |
rs12010369 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | BRWD3 | GRCh38.p7 | X:80767232 | tgagcacaaagaacc[A/G]acaaactgcctcctc | 254065 |
rs12012250 | snp | A/G | 0.204314 | 0.24579 | intron-variant | BRWD3 | GRCh38.p7 | X:80803946 | GTGAGGATCAAATGA[A/G]ATAATGTGAAAACAC | 254065 |
rs12012589 | snp | G/T | 0.194041 | 0.243657 | intron-variant | BRWD3 | GRCh38.p7 | X:80754263 | cctagattttggggg[G/T]ttttttgtagctatt | 254065 |
rs12016606 | snp | A/C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80770232 | tagaaaaagagggaa[A/C/T]cctccctaactcatt | 254065 |
rs12556865 | snp | A/G | 0.379788 | 0.213671 | intron-variant | BRWD3 | GRCh38.p7 | X:80739282 | agttgaaagcatggt[A/G]ttgccatttgtttgg | 254065 |
rs12557771 | snp | C/T | 0.40894 | 0.192972 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810509 | GCCGTGAAGCATGTT[C/T]CCCCTTCTGAAAGTT | 254065 |
rs12558264 | snp | G/T | 0.405517 | 0.195741 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811011 | TGCCACTGACCACAG[G/T]GGGCCTTGAATTTCT | 254065 |
rs12686966 | snp | C/T | 0.0974994 | 0.1981 | intron-variant | BRWD3 | GRCh38.p7 | X:80706360 | gtgatccttccacct[C/T]ggcctccaaaagtgc | 254065 |
rs12687186 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80782419 | actaaaagaaaacat[C/T]ggtgaaactctccag | 254065 |
rs12687265 | snp | A/G | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80800657 | CATAAAAAATTAACT[A/G]GGTTTTCTCTTTTTG | 254065 |
rs12687572 | snp | A/G | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80755884 | TACACTATCAACTAT[A/G]TAAATTTATGCACAA | 254065 |
rs12688645 | snp | C/G | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80802975 | ccgggcgtagcgggc[C/G]cctgtagtcccagct | 254065 |
rs12688766 | snp | C/T | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80803026 | agaatggcgtgaacc[C/T]gggaggcggagcttg | 254065 |
rs12688780 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80788153 | ACACTGGTAATAAAA[C/T]AGGgccagggacagt | 254065 |
rs12689010 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80768529 | acagacaagcaaacg[C/T]tgagagattttgtca | 254065 |
rs12689069 | snp | C/G | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80785933 | tacttgggaggttga[C/G]gcaggagaatcactt | 254065 |
rs12689101 | snp | A/C | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80800142 | ATATAAGAAAAGTTC[A/C]CAAGACAGAAAGGGA | 254065 |
rs12689192 | snp | A/C | 0.299752 | 0.244999 | intron-variant | BRWD3 | GRCh38.p7 | X:80691687 | CTGCTAATATTAAAA[A/C]TAGAATCACTGTGCT | 254065 |
rs12689362 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80782474 | tgatttgttgactaa[C/T]accccaaaagcacag | 254065 |
rs12690214 | snp | G/T | 0.447863 | 0.152807 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671128 | TTTTAAAATGTCAGG[G/T]ACATATAACTCAGCT | 254065 |
rs12690260 | snp | A/G | 0.0974994 | 0.1981 | intron-variant | BRWD3 | GRCh38.p7 | X:80768977 | ctttaaatcaacaaa[A/G]atcaaaagaaacaaa | 254065 |
rs12747867 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770198 | ATTGGAATAGTTTCA[C/G]AAGGAATGGTACCAG | 254065 |
rs12798365 | snp | C/G/T | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80770143 | AAGTCCAGGACCAGA[C/G/T]GAATTCACAGCCGAA | 254065 |
rs12835440 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80753257 | tatttttgttattgt[G/T]gcctgtgcttttcag | 254065 |
rs12840808 | snp | G/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80690573 | CGTCAGTAGGAGACT[G/T]GGATGACAGAGGGAC | 254065 |
rs12841491 | snp | A/G | 0.0560809 | 0.157783 | intron-variant | BRWD3 | GRCh38.p7 | X:80773987 | ATATTTGGTGTTCAC[A/G]TATTTGCTGAATTGA | 254065 |
rs12844416 | snp | C/T | 0.0271702 | 0.113344 | intron-variant | BRWD3 | GRCh38.p7 | X:80716743 | caattgagttgtttc[C/T]accatttggttattg | 254065 |
rs12844417 | snp | A/C | 0.0271702 | 0.113344 | intron-variant | BRWD3 | GRCh38.p7 | X:80716746 | ttgagttgtttccac[A/C]atttggttattgtga | 254065 |
rs12853961 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756525 | aaaaaaaaaaaaaaa[A/G]gaaaCAATGTCAACA | 254065 |
rs16979508 | snp | A/C | 0.447692 | 0.153029 | intron-variant | BRWD3 | GRCh38.p7 | X:80799865 | TAATGATAACTATCT[A/C]CTAAAGTTCGGTTAG | 254065 |
rs16979519 | snp | A/G | 0.379007 | 0.214143 | intron-variant | BRWD3 | GRCh38.p7 | X:80685124 | TGACCAAAATTTAAA[A/G]GACTCAGACTGCTTG | 254065 |
rs17281706 | snp | A/G | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80775403 | GCTTTACTTGACACA[A/G]TTGGGGCCCAGAGTA | 254065 |
rs17281713 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80777733 | TGAATAACATAACTC[C/T]TGGGCAATTTTATCT | 254065 |
rs17332994 | snp | A/G | 0.097024 | 0.197733 | intron-variant | BRWD3 | GRCh38.p7 | X:80684415 | GAATAGAAAATCCAT[A/G]GCCGTTGGCTTCATC | 254065 |
rs28361314 | snp | A/G | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80705612 | CTTACACAAACCTAG[A/G]CAGTATAGCCTACTA | 254065 |
rs28417201 | snp | C/T | 0.447863 | 0.152807 | intron-variant | BRWD3 | GRCh38.p7 | X:80701050 | TTCAGTCTACACATT[C/T]CATATAAACAGTATA | 254065 |
rs28624834 | snp | A/C | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80730940 | TACCAAAATTTTTTC[A/C]ATTAATCCCTTAATG | 254065 |
rs28645736 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80725854 | ATGTGTTACATGCCT[A/G]TATAACATAACATGT | 254065 |
rs28816472 | snp | C/G | 0.0312828 | 0.12109 | intron-variant | BRWD3 | GRCh38.p7 | X:80783310 | AGAAACACTTGAACC[C/G]GGGAGGCAGAGGTTG | 254065 |
rs33967268 | in-del | -/AT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726007 | CATAACATGTTTACA[-/AT]TGTTATATGTCTATA | 254065 |
rs34087289 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80729733 | AATCAGCAATGTTCC[-/C]TGTCATCCACTCTGT | 254065 |
rs34154839 | in-del | -/A | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670979 | TGTTTGCCACTGGGA[-/A]GACAAATTCTGGGTA | 254065 |
rs34291381 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801215 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 254065 |
rs34297254 | in-del | -/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80710102 | CTCATCAGAAAAAAA[-/T]TTCTCCATATTGACA | 254065 |
rs34309179 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710176 | CTGTTACGTAATTTT[-/T]ATGTGCCAGGAGTGT | 254065 |
rs34359335 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770499 | GAGATAATCATGTGG[-/T]TTTTTGTCTTTGTTT | 254065 |
rs34424596 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80777152 | TTAAGACCCCCCCCC[-/C]ACGAAAAACCTCCTG | 254065 |
rs34531484 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801053 | GCTCAGTAGAGAAAA[-/A]GTCCAACAAAAGAAC | 254065 |
rs34536922 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770436 | CGTATGTTGAACCAG[-/C]CCTTGCATCCCAGGG | 254065 |
rs34615565 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80798092 | GAGCGAGACTCCACC[-/C]TCAAAAACATAAATT | 254065 |
rs34683917 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732039 | CTTGTGATGGGTCAC[-/C]ATTAGTCAAAACTTT | 254065 |
rs34736873 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769954 | GTTTGTAGTACTCTC[-/C]TGATGGTAGTTTGTA | 254065 |
rs34748953 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770548 | CTTTGACAAAATTCA[A/G]CAGCCTTTTATGCTA | 254065 |
rs34780882 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806873 | GTCTAGTAAACTGGG[-/G]TTGTTGGGGTTTTTT | 254065 |
rs34820109 | snp | A/C | 0.05658 | 0.158394 | intron-variant | BRWD3 | GRCh38.p7 | X:80730142 | AAAATGGTACAGTCA[A/C]TTTGGAAAACAGCTT | 254065 |
rs34829054 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761892 | AGAAAGGCCCATTTT[-/T]GTAGAAATCATAAGC | 254065 |
rs34984796 | snp | C/T | 0.00216947 | 0.0328638 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80681423 | TTCTTCATCGAGCTT[C/T]GGTGGATATAGCCGA | 254065 |
rs34993037 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800874 | ATTTCTTTTTCTTTT[-/T]ATTAGTTTTAAGATT | 254065 |
rs35011251 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80806279 | AGAATATTTAAAAGA[-/C]TACGTTAAAATTGAG | 254065 |
rs35097422 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732041 | TTGTGATGGGTCACA[A/T]TAGTCAAAACTTTGT | 254065 |
rs35140864 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730078 | TAAATCACTTTTTTT[-/T]GATAATATAAGTAAC | 254065 |
rs35195011 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750930 | AAGGAAAGAAATTGG[-/G]AAATTATGCCATTCA | 254065 |
rs35202356 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800268 | TTTTTTTTTTTTTTT[-/T]AATGAAAAACCCCAG | 254065 |
rs35207982 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80732813 | AATTATATTCCATAG[-/C]ACAGAGAAGAGGAAA | 254065 |
rs35220611 | in-del | -/GTGT | 0.499597 | 0.0141815 | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676333 | TCTGTGTTGTGTTTC[-/GTGT]GTGTGTGTCTGTGTG | 254065 |
rs35233064 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80728716 | AAATAATGTGCTTTT[-/T]GACCATTTTAATTAC | 254065 |
rs35254333 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770137 | CAAAAAAAGTCCAGG[A/G]CCAGATGGATTCACA | 254065 |
rs35385151 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80704261 | AAACACCAAAAAACA[-/TA]GTGGAATGGAGGGAG | 254065 |
rs35388171 | in-del | -/GA | | | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809845 | AGAGAGAGAGAGAGA[-/GA]TAGACGGAGCGAGAA | 254065 |
rs35466607 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80723338 | AGTTAGCTCCCAAAG[-/T]ATTTCAACAGGATCA | 254065 |
rs35678169 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796944 | TTGGGAGGCCGAGGA[-/A]GGGAGGGTTGCTTGA | 254065 |
rs35738976 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80718988 | TCTACTGGTATTAAG[-/C]ATCAAACTATTATAA | 254065 |
rs35759194 | in-del | -/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80697561 | ACCCATTTGTAAGAG[-/C]AGGGCGTGTGGTATT | 254065 |
rs35833024 | in-del | -/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670877 | TAAATGCATTTTTTT[-/T]ATTCTAAATACACAA | 254065 |
rs35861459 | in-del | -/A | 0.0287145 | 0.11633 | intron-variant | BRWD3 | GRCh38.p7 | X:80732577 | GAATAAAGGAGAAAG[-/A]AAGTAGGAGAGAGAG | 254065 |
rs35899747 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80734771 | GAAAGCACTGTAAAA[-/A]GTGTTTTCAATATGG | 254065 |
rs35915410 | in-del | -/A | | | intron-variant | BRWD3 | GRCh38.p7 | X:80683550 | ATTTCAAAAGAAAAA[-/A]CTTGATTACTATTTT | 254065 |
rs36052041 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80689127 | GGGATGAATTGTTTT[-/T]CCAGTAAAGATTTGT | 254065 |
rs36087196 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773015 | ATTGATAGAACTTTT[-/T]CTTGAAATGACAGAA | 254065 |
rs36106648 | in-del | -/GCA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80721496 | AGCCTTAATTCCCTA[-/GCA]ATGATATGAAATTCT | 254065 |
rs36173381 | snp | G/T | 0.375 | 0.216506 | intron-variant | BRWD3 | GRCh38.p7 | X:80770655 | ATATCATACTGAATG[G/T]GCAAAAACTGGAAGC | 254065 |
rs36177600 | multinucleotide-polymorphism | AA/TG | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770686 | ATTCCCTTTGAAAAC[AA/TG]GCACAAGACAGGGAT | 254065 |
rs41300175 | snp | G/T | 0.0261392 | 0.111294 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675573 | ATTATTAACAACCTC[G/T]CAGCTTATAACTTAT | 254065 |
rs41300183 | snp | A/C | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674168 | CTTAATAACTGAAAT[A/C]AACATTACAGCAAAA | 254065 |
rs41300244 | snp | C/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671467 | ATCTCTAAAGCTGAA[C/T]AGGTAACTCCATATT | 254065 |
rs41300257 | snp | A/T | 0.0699487 | 0.17344 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675237 | ATAATGATTCACAAC[A/T]TGAGTGTGCAGTGCA | 254065 |
rs41306245 | snp | A/C | 0.0709308 | 0.174454 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671148 | ATAACTCAGCTGTTA[A/C]AAGTTGTAAGTCATA | 254065 |
rs41307391 | snp | A/C | 0.00475684 | 0.0485365 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671476 | GCTGAATAGGTAACT[A/C]CATATTTCTTTCTTC | 254065 |
rs41310717 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676357 | TGTCTGTGTGTGTGT[A/G]TGTGTGTGTATGTGT | 254065 |
rs41311569 | snp | A/C | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671800 | GGATACCAAGAACAA[A/C]AAAAAGGTACAGTTA | 254065 |
rs45496995 | snp | C/T | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80687638 | TAAGACAGTTTACTG[C/T]ACCTAGACAGTATAA | 254065 |
rs45610632 | snp | C/T | 0.30706 | 0.243401 | intron-variant | BRWD3 | GRCh38.p7 | X:80736255 | TAGATTAATAAATAC[C/T]TTATAAAAAATTTAA | 254065 |
rs45627037 | snp | C/G | 0.348057 | 0.229967 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672759 | TCGAAAGTTCCATCC[C/G]TTCCCCTAGAACTAT | 254065 |
rs55698138 | snp | A/G | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80695076 | AGTTTCCCACATGTT[A/G]TTCTTGTGATGGTGA | 254065 |
rs55787046 | snp | A/G | 0.204314 | 0.24579 | intron-variant | BRWD3 | GRCh38.p7 | X:80796256 | CTGCCTCAGCCTCAC[A/G]AGTAGCTGGGATTAG | 254065 |
rs55824836 | snp | C/G | 0.0391916 | 0.134387 | intron-variant | BRWD3 | GRCh38.p7 | X:80744022 | AGCTAAATTTTATCA[C/G]TTTTCTTACCTGTAT | 254065 |
rs55934435 | snp | C/T | 0.0590711 | 0.161388 | intron-variant | BRWD3 | GRCh38.p7 | X:80718074 | GAGATTTACAAATGT[C/T]TATTAGTACTAGTTC | 254065 |
rs56115230 | snp | C/T | 0.132596 | 0.220718 | intron-variant | BRWD3 | GRCh38.p7 | X:80728720 | AATGTGCTTTTTGAC[C/T]ATTTTAATTACTCTA | 254065 |
rs56311451 | in-del | -/AAGA/AAGAAAGA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80730450 | AGAAAGAAAGAAAGA[-/AAGA/AAGAAAGA]CACAGTTAACACAGA | 254065 |
rs56332927 | snp | C/T | 0.16651 | 0.235647 | intron-variant | BRWD3 | GRCh38.p7 | X:80694546 | AGCTGGGAAAGGGGA[C/T]ATACCCTGCGAAGCC | 254065 |
rs56386414 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725816 | TACATGTGTTACATG[C/T]CTATATAACATAACA | 254065 |
rs56387795 | snp | C/T | 0.16651 | 0.235647 | intron-variant | BRWD3 | GRCh38.p7 | X:80703745 | ATTTGAATGATTTTG[C/T]TTTATTATATACAAT | 254065 |
rs56396812 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800552 | CTCAAAAAAAAAAAA[-/AA]TACAAATACAAATAC | 254065 |
rs56405068 | snp | A/C | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80802269 | CAACACGGTGAAACT[A/C]CACCTCTACTGAAAA | 254065 |
rs56413325 | in-del | -/C | 0.0510748 | 0.151422 | intron-variant | BRWD3 | GRCh38.p7 | X:80799773 | GAATCTTTGCAGCAT[-/C]CCCAGTTACTACTTA | 254065 |
rs57027733 | snp | C/T | 0.348641 | 0.229717 | intron-variant | BRWD3 | GRCh38.p7 | X:80799516 | TAAAATGTAACATTT[C/T]GCCTGGGTCTGATTG | 254065 |
rs57129345 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80797221 | AGCTTATTCCTTTTT[C/T]CCCAAAACTGTCTTA | 254065 |
rs57187877 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80793161 | AAAAAAAAAAAAAAA[-/AA]ATTACTGATAGGTTG | 254065 |
rs57489571 | snp | A/G | 0.0199298 | 0.0978146 | intron-variant | BRWD3 | GRCh38.p7 | X:80764329 | TTTTTTTTTAGAGAC[A/G]GAGTCTCGCTCTGTT | 254065 |
rs57542096 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80735406 | AGTATTATTACTATA[G/T]TTTTATTAACCATAT | 254065 |
rs57689523 | snp | A/G | 0.379268 | 0.213986 | intron-variant | BRWD3 | GRCh38.p7 | X:80705123 | ATACAAAAATTAGCC[A/G]GGTGTGATGGCACAC | 254065 |
rs57890773 | snp | C/T | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80688104 | CAGGACCGTCTGAAT[C/T]TAAATCAACAATTTC | 254065 |
rs57923356 | in-del | -/AT/TA | 0.223604 | 0.248603 | intron-variant | BRWD3 | GRCh38.p7 | X:80786517 | TATATATATATATAT[-/AT/TA]GGAGTCTTGCTCTGT | 254065 |
rs57997309 | in-del | -/GG | | | intron-variant | BRWD3 | GRCh38.p7 | X:80808773 | ATGGGGGGGGGGGGG[-/GG]AAGGGGGGTCGAGAA | 254065 |
rs58148585 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80764486 | ATTTTTTTTTTTTTT[-/T]GTATTTTTAGTATAG | 254065 |
rs58601634 | in-del | -/CAC | 0.0098997 | 0.0696552 | intron-variant | BRWD3 | GRCh38.p7 | X:80744297 | AATGAAGCAGAAATT[-/CAC]CACAATACCCCCACC | 254065 |
rs58761845 | in-del | -/TATATATATATATATATATATA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80700442 | TATTTGATATATATA[-/TATATATATATATATATATATA]ACAATACAATTAGGC | 254065 |
rs59015778 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80731474 | GTGGTTTTTTCATTC[C/T]TAATACAGACATCAC | 254065 |
rs59358158 | snp | C/T | 0.386699 | 0.209316 | intron-variant | BRWD3 | GRCh38.p7 | X:80809136 | CGCTGACCGTTTGAC[C/T]AGTCAAGGCCGGCCT | 254065 |
rs59394410 | in-del | -/ACAC/ACACACAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80750893 | CACACACACACACAC[-/ACAC/ACACACAC]GCAAAAATCATTAAG | 254065 |
rs59483641 | snp | C/T | 0.058837 | 0.161111 | intron-variant | BRWD3 | GRCh38.p7 | X:80682118 | AAAAATATGTAACAA[C/T]GAGCATTTTTTTTTT | 254065 |
rs59916134 | in-del | -/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789393 | TTTTTTTCTTTTTTT[-/T]GAGACGGAGTCTCGC | 254065 |
rs60034239 | in-del | -/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669002 | GTCTTTTTTTTTTTT[-/T]AAGTCATTTCTTATC | 254065 |
rs60181151 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80776569 | CTAGGACTGAAAAAA[A/G]AAAAAAGCAACCATG | 254065 |
rs60485182 | in-del | -/A | 0.0515767 | 0.15208 | intron-variant | BRWD3 | GRCh38.p7 | X:80688995 | TTTCATGAAAAAAAT[-/A]AAAAAAAACAGCATT | 254065 |
rs60751934 | snp | A/T | 0.379788 | 0.213671 | intron-variant | BRWD3 | GRCh38.p7 | X:80807766 | TTCCATTTTTAAATA[A/T]GTCCATTGTTGTCTC | 254065 |
rs60939653 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80771452 | AATAACACCACACAT[A/C]TACAACCATCTGATC | 254065 |
rs61147520 | snp | C/G | 0.018891 | 0.0953342 | intron-variant | BRWD3 | GRCh38.p7 | X:80781349 | GTTTTTGCCTAATTA[C/G]GATTTGAGTGAGCTA | 254065 |
rs61306754 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80803124 | AAAAAAAAAAAAAAA[-/AA]GAAATGTCAAGCAAG | 254065 |
rs61582359 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80751412 | TGAATGAAACAAACA[A/G]AAAGAGAAGGACAGC | 254065 |
rs62211732 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770450 | GACTGGTTCAATATA[A/C/T]GCAAATCAATAAATG | 254065 |
rs62605569 | snp | A/G | 0.375331 | 0.216315 | intron-variant | BRWD3 | GRCh38.p7 | X:80686213 | AGGTGGGAATTGAAC[A/G]ATGAGAACACTTGAA | 254065 |
rs62605572 | snp | C/T | 0.348057 | 0.229967 | intron-variant | BRWD3 | GRCh38.p7 | X:80711056 | CCCATTCATAATTTA[C/T]GTATGCCACATTATT | 254065 |
rs62605574 | snp | C/T | 0.308046 | 0.243168 | intron-variant | BRWD3 | GRCh38.p7 | X:80718811 | AAAAATCTCATAAGA[C/T]GACTACATTTGAAAA | 254065 |
rs62605575 | snp | C/T | 0.299416 | 0.245067 | intron-variant | BRWD3 | GRCh38.p7 | X:80723528 | AGGAATGTTTATATC[C/T]TCATCACCCTATAAC | 254065 |
rs62605576 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80727318 | ACTCTCATGTCATTC[C/T]TTTGCTTTAAACCCT | 254065 |
rs62605577 | snp | C/T | 0.348057 | 0.229967 | intron-variant | BRWD3 | GRCh38.p7 | X:80727451 | GTGATATAGCTAAAT[C/T]GGCTTTCTTTCAGCT | 254065 |
rs62605604 | snp | A/C | 0.49967 | 0.0128434 | intron-variant | BRWD3 | GRCh38.p7 | X:80741470 | TCTAGTTCCAAATGC[A/C]TGAGGAATGGCCACA | 254065 |
rs62605605 | snp | A/G | 0.300756 | 0.244793 | intron-variant | BRWD3 | GRCh38.p7 | X:80765731 | ATATGAATTGATGTT[A/G]ATTTTACCTCATTGT | 254065 |
rs62605606 | snp | A/G | 0.345123 | 0.231196 | intron-variant | BRWD3 | GRCh38.p7 | X:80767276 | ACCCCTGTGTAGCCT[A/G]ACTGGGAGACACTTC | 254065 |
rs62605608 | snp | C/T | 0.0520783 | 0.152732 | intron-variant | BRWD3 | GRCh38.p7 | X:80770546 | GCCTTTGACAAAATT[C/T]AACAACGCTTCATGC | 254065 |
rs62605609 | snp | A/G | 0.0520783 | 0.152732 | intron-variant | BRWD3 | GRCh38.p7 | X:80770551 | TGACAAAATTCAACA[A/G]CGCTTCATGCTAAAA | 254065 |
rs62605615 | snp | C/G | 0.348057 | 0.229967 | intron-variant | BRWD3 | GRCh38.p7 | X:80804331 | CAACCTCTGCTTCCA[C/G]GGCTCAAGCAATTCT | 254065 |
rs66509523 | in-del | -/ACTT/CTTA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80727722 | ATCAAGGAGTTGACA[-/ACTT/CTTA]AGTTGAGATTGGGTA | 254065 |
rs67192777 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80704261 | AAACACCAAAAAACA[C/T]AGTGGAATGGAGGGA | 254065 |
rs67376083 | in-del | -/CAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744298 | ATGAAGCAGAAATTC[-/CAC]ACAATACCCCCACCC | 254065 |
rs67429303 | snp | G/T | 0.203499 | 0.245637 | intron-variant | BRWD3 | GRCh38.p7 | X:80683353 | TTTTCTTCTTTATAC[G/T]TCTGTGTTTCCCAAA | 254065 |
rs67638903 | in-del | -/AT | 0.499361 | 0.0178694 | intron-variant | BRWD3 | GRCh38.p7 | X:80704260 | AAAACACCAAAAAAC[-/AT]AGTGGAATGGAGGGA | 254065 |
rs71172658 | in-del | -/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770494 | AATCATGTGGTTTTT[-/T]GTCTTTGTTTCTGTT | 254065 |
rs71529330 | snp | A/C | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770368 | TAAAATACTGGCAAA[A/C]CAAATCCAGCAGCAC | 254065 |
rs71671860 | in-del | -/CTT | 0.499656 | 0.0131081 | intron-variant | BRWD3 | GRCh38.p7 | X:80684645 | GTTTGTGCCTTTCTC[-/CTT]CTTGATTTTAAATCA | 254065 |
rs71779166 | in-del | -/GT | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726377 | GTTTACATGTTATAT[-/GT]CTGTATAACATAACA | 254065 |
rs71904190 | in-del | -/A | 0.216411 | 0.247733 | intron-variant | BRWD3 | GRCh38.p7 | X:80726993 | CAATGTACATTAGGG[-/A]AAAAAAAAAACTTTG | 254065 |
rs72065200 | in-del | -/TA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80687101 | CTATCTGTATGTGTG[-/TA]TATATATATATATAT | 254065 |
rs72082762 | in-del | -/AT | 0.208779 | 0.246578 | intron-variant | BRWD3 | GRCh38.p7 | X:80726027 | ATATGTCTATATAAC[-/AT]ATAACATGTTTACAT | 254065 |
rs72409761 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80808774 | ATGGGGGGGGGGGGG[-/AA]GGGGGGTCGAGAAGG | 254065 |
rs72630851 | snp | A/C | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675848 | TTGTCTAGATTGATA[A/C]CTCAAGTATTCTTTT | 254065 |
rs73225392 | snp | C/G | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80679673 | AATCAATAGAGTATA[C/G]AAGCTTACAAGTAGA | 254065 |
rs73225394 | snp | C/G | 0.166942 | 0.2358 | intron-variant | BRWD3 | GRCh38.p7 | X:80687296 | TTCTTTCCTCTACAA[C/G]ATCAAGTTATAGAGC | 254065 |
rs73225401 | snp | A/G | 0.163474 | 0.234549 | intron-variant | BRWD3 | GRCh38.p7 | X:80711057 | CCATTCATAATTTAC[A/G]TATGCCACATTATTC | 254065 |
rs73225402 | snp | C/T | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80711605 | GTCTGAAAAGAAACA[C/T]TTGCAACCTACTCTC | 254065 |
rs73227304 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80725927 | CATGCCTATATGACA[C/T]AACTTGTTTACATGT | 254065 |
rs73227308 | snp | C/T | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80738443 | ATTAGCATCATACCA[C/T]TTTAACTATATTTTG | 254065 |
rs73227310 | snp | G/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80748443 | CTCTTCAATTTTTTG[G/T]AAGAGTTTGAAAAAC | 254065 |
rs73227312 | snp | C/T | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80749139 | CTATCCTGGAGAATA[C/T]TCCACATGTACTTGA | 254065 |
rs73227313 | snp | C/T | 0.207159 | 0.246302 | intron-variant | BRWD3 | GRCh38.p7 | X:80750893 | ACACACACACACACA[C/T]GCAAAAATCATTAAG | 254065 |
rs73227314 | snp | G/T | 0.447521 | 0.15325 | intron-variant | BRWD3 | GRCh38.p7 | X:80752203 | TGTTGTTTTAGAGAT[G/T]GGGTCTCTCTATGTT | 254065 |
rs73227316 | snp | G/T | 0.167375 | 0.235951 | intron-variant | BRWD3 | GRCh38.p7 | X:80752967 | ACCACGCCTGGCCGA[G/T]CATTTTTTTGTATAC | 254065 |
rs73227318 | snp | C/T | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80758994 | TATTGTGGTTACTTT[C/T]TTCTGGGAGGTCTCT | 254065 |
rs73227321 | snp | A/G | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80764892 | AAAAAGGATATACAT[A/G]TGGTAAATAAGCATA | 254065 |
rs73227322 | snp | C/T | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80765839 | TATTTCAGTTGTATG[C/T]AAACAGATATATCAT | 254065 |
rs73227323 | snp | C/G | 0.167375 | 0.235951 | intron-variant | BRWD3 | GRCh38.p7 | X:80766861 | CCCTTTCCTAGCCAA[C/G]GGAAGCCTTGAGAGA | 254065 |
rs73227324 | snp | C/G | 0.167375 | 0.235951 | intron-variant | BRWD3 | GRCh38.p7 | X:80767159 | AGAAACTTCTGCACA[C/G]GTAAACCTCCCTGTC | 254065 |
rs73227326 | snp | C/T | 0.102711 | 0.202005 | intron-variant | BRWD3 | GRCh38.p7 | X:80772735 | TCCCCAATTACAAAC[C/T]TGGGCATTTATCCCA | 254065 |
rs73227327 | snp | G/T | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80774784 | TCCAAAATCTTGCTT[G/T]AATCAATCCAATTAC | 254065 |
rs73227329 | snp | C/T | 0.0204488 | 0.0990265 | intron-variant | BRWD3 | GRCh38.p7 | X:80775646 | GGCAGGATACTTTTG[C/T]GCAAAGAGCACTAGA | 254065 |
rs73227335 | snp | A/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80786134 | TTACTCTAGATCCAC[A/T]CTATCCAATATAGTG | 254065 |
rs73227338 | snp | A/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80789752 | AAAAGCTACGAAAAG[A/T]ACACCATTCATTTAA | 254065 |
rs73227339 | snp | C/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80791517 | GGAAAACAACACATA[C/T]AAATAATGTACTTTT | 254065 |
rs73227340 | snp | A/C | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80796107 | AATAAAAATCAAAGT[A/C]AAGTCTAACTATAAT | 254065 |
rs73227341 | snp | A/C | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80800078 | AAGTAAGGTACACCT[A/C]ATTTTGCCTAGAGGT | 254065 |
rs73227344 | snp | A/G | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80804582 | AAAAATGATTTAAAA[A/G]TCTTAAAATGTGGTT | 254065 |
rs73502699 | snp | A/T | 0.0228475 | 0.104411 | intron-variant | BRWD3 | GRCh38.p7 | X:80691039 | TTATAATAAGTGATT[A/T]AAAAAAAACAGACCT | 254065 |
rs73502700 | snp | G/T | 0.189048 | 0.242456 | intron-variant | BRWD3 | GRCh38.p7 | X:80693839 | AAGCAGAGCATTAAA[G/T]TTCAGAACTTTTGCA | 254065 |
rs73504604 | snp | A/G | 0.11536 | 0.210647 | intron-variant | BRWD3 | GRCh38.p7 | X:80700309 | ATCAGCTTCATAAGT[A/G]TGCTGAAGAAGCAGA | 254065 |
rs73504605 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725987 | ACATGTTATATGTCT[A/G]TATAACATAACATGT | 254065 |
rs73504608 | snp | A/G | 0.000508699 | 0.0159402 | intron-variant | BRWD3 | GRCh38.p7 | X:80736119 | ATCTGATTCAAATAA[A/G]AAGTTTTCATGTTCA | 254065 |
rs73504627 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80766088 | TGATTAACATTTGAA[C/T]TGGTAGACAGAGTAA | 254065 |
rs73504642 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80807852 | TATTTAGTGAAAACG[A/G]GTCTATGCAAATGCG | 254065 |
rs73630397 | snp | C/T | 0.0199298 | 0.0978146 | intron-variant | BRWD3 | GRCh38.p7 | X:80687472 | CAGTATTTCAAAATA[C/T]ATTGTCCCTTATATA | 254065 |
rs73630398 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | BRWD3 | GRCh38.p7 | X:80708062 | GATTAGGATTTGTTT[C/T]AAAAGTACAACCGCA | 254065 |
rs74351120 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770445 | ATTGATTTGCTTATG[C/T]TGAACCAGCCTTGCA | 254065 |
rs74437935 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770496 | ATAATCACATGGTTT[C/T]TGTCATTGGTTCTGT | 254065 |
rs74553758 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770369 | AAAATACTGGCAAAC[C/T]GAATCCAGCAGCACT | 254065 |
rs74571923 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80790642 | TTAAAAGAAAAAAAA[A/G]GCGAGAGAAGGGAAG | 254065 |
rs74630144 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80708829 | CAAAAAAAAAAAAAA[A/G]GAATTGGGAATGGCA | 254065 |
rs74639040 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749086 | TATTTCAATCTTCTT[A/G]AATTTGTTAAGACTT | 254065 |
rs74704167 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792140 | GGTAACCACCCAACA[A/C]CTTAACATATCATCT | 254065 |
rs74754568 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80686045 | TAATTTTTTATGGCT[A/G]CATAGTATTCCATGG | 254065 |
rs74873035 | snp | A/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80703134 | TGTTTTGTTTTTTTT[A/T]AATAAATATTGGAAC | 254065 |
rs74981748 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80726078 | ACATGTTTACATGTT[A/G]TCTGTATAACAACAT | 254065 |
rs75039016 | snp | A/C | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749080 | TAATATTATTTCAAT[A/C]TTCTTAAATTTGTTA | 254065 |
rs75512353 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80748208 | TGTTGAATTTTGTCA[A/G]ATACTATTTCTGCAT | 254065 |
rs75603757 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749103 | ATTTGTTAAGACTTG[C/T]TTTGTGTCCTAAAAT | 254065 |
rs75721815 | snp | A/G | 0.277778 | 0.248452 | intron-variant | BRWD3 | GRCh38.p7 | X:80770507 | CACAAAAACCACATG[A/G]TTATCTCAATAGACA | 254065 |
rs75761213 | snp | C/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80709035 | TGATCTCTATGAGGG[C/G]TGAAGTCAATAATAA | 254065 |
rs75859570 | snp | G/T | 0.301091 | 0.244724 | intron-variant | BRWD3 | GRCh38.p7 | X:80704143 | GCTGAGGTGGGAGTA[G/T]TGCTTGAGCCTAGCA | 254065 |
rs76038515 | snp | A/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749084 | ATTATTTCAATCTTC[A/T]TAAATTTGTTAAGAC | 254065 |
rs76154204 | snp | A/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80800268 | TTTTTTTTTTTTTTT[A/T]AATGAAAAACCCCAG | 254065 |
rs76263767 | snp | C/T | 0.5 | 0 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80668990 | AGCAACAGTCTAGTC[C/T]TTTTTTTTTTTTAAG | 254065 |
rs76294110 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80713113 | CCCGTCCGGGAGGTG[A/G]GGGGCACCTCTGCCC | 254065 |
rs76524485 | snp | G/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749110 | AAGACTTGCTTTGTG[G/T]CCTAAAATACGATCT | 254065 |
rs76777790 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80790217 | AAAAAAAAAAAAAAA[A/G]AGATATACCTTCATG | 254065 |
rs77049794 | in-del | -/ACTT/CTT | 0.447692 | 0.153029 | intron-variant | BRWD3 | GRCh38.p7 | X:80736705 | CAAGTTAAAAAAAAA[-/ACTT/CTT]AAGTTGTCAATACAG | 254065 |
rs77145988 | snp | G/T | 0.348057 | 0.229967 | intron-variant | BRWD3 | GRCh38.p7 | X:80700928 | TAATGTCCTTGTAGA[G/T]TCTGTTATTTGCAAG | 254065 |
rs77390526 | snp | C/T | 0.5 | 0 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80668989 | TAGCAACAGTCTAGT[C/T]TTTTTTTTTTTTTAA | 254065 |
rs77392979 | snp | A/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749094 | TCTTCTTAAATTTGT[A/T]AAGACTTGCTTTGTG | 254065 |
rs77395071 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80790219 | AAAAAAAAAAAAAAA[A/G]ATATACCTTCATGAT | 254065 |
rs77549203 | snp | C/G | 0 | 0 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810869 | CACCCCACTCCCTCA[C/G]CTAAACCTGATGAGA | 254065 |
rs77655104 | in-del | -/CAC | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744299 | TGAAGCAGAAATTCA[-/CAC]CCATACCCCCACCCA | 254065 |
rs77684772 | snp | G/T | 0.283335 | 0.247768 | intron-variant | BRWD3 | GRCh38.p7 | X:80680199 | AAACTTCAAATAGCT[G/T]AACATGTTAGAACTT | 254065 |
rs77721987 | snp | G/T | 0.444444 | 0.157135 | intron-variant | BRWD3 | GRCh38.p7 | X:80777385 | AAGTATACAAATTAG[G/T]GGTATTATTATTATT | 254065 |
rs77918504 | snp | A/G | 0.043513 | 0.140937 | intron-variant | BRWD3 | GRCh38.p7 | X:80749121 | TGTGTCCTAAAATAC[A/G]ATCTATCCTGGAGAA | 254065 |
rs78021323 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749120 | TTGTGTCCTAAAATA[C/T]GATCTATCCTGGAGA | 254065 |
rs78324209 | snp | A/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80703136 | TTTTGTTTTTTTTTA[A/T]TAAATATTGGAACAT | 254065 |
rs78324441 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80774975 | TATGATTTTCCTATT[A/C]AAAAACATCCAATGA | 254065 |
rs78389643 | snp | A/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749071 | AAAGATGCTTAATAT[A/T]ATTTCAATCTTCTTA | 254065 |
rs78431326 | in-del | -/T | 0.078261 | 0.181675 | intron-variant | BRWD3 | GRCh38.p7 | X:80764313 | GGGCTAGGCAAAGAA[-/T]TTTTTTTTTAGAGAC | 254065 |
rs78454193 | snp | A/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80809367 | AATAGAAGCTTTTTC[A/T]AAAGAAACTGACAGC | 254065 |
rs78648461 | snp | G/T | 0.444444 | 0.157135 | intron-variant | BRWD3 | GRCh38.p7 | X:80777388 | TATACAAATTAGTGG[G/T]ATTATTATTATTTTT | 254065 |
rs78749589 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726376 | ATGTTTACATGTTAT[A/G]TCTGTATAACATAAC | 254065 |
rs78935190 | snp | C/G/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80733276 | CCTGATAGGCTATGG[C/G/T]TACTACTTGGATGAG | 254065 |
rs78998305 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749082 | ATATTATTTCAATCT[C/T]CTTAAATTTGTTAAG | 254065 |
rs79136434 | in-del | -/AGC | 0.299081 | 0.245135 | intron-variant | BRWD3 | GRCh38.p7 | X:80721495 | AAGCCTTAATTCCCT[-/AGC]AATGATATGAAATTC | 254065 |
rs79241332 | snp | C/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749102 | AATTTGTTAAGACTT[C/G]CTTTGTGTCCTAAAA | 254065 |
rs79273290 | snp | A/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80800270 | TTTTTTTTTTTTTTA[A/T]TGAAAAACCCCAGGG | 254065 |
rs79448016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | BRWD3 | GRCh38.p7 | X:80770505 | TCTATTGAGATAATC[A/G]TGTGGTTTTTGTCCT | 254065 |
rs79515307 | snp | C/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80770426 | ACCAGCCTTGCATCC[C/G]AGGGATGAAGCCCAC | 254065 |
rs79527295 | snp | A/G | 0.0358881 | 0.129059 | intron-variant | BRWD3 | GRCh38.p7 | X:80713668 | TCCCCCTCTGCGAGA[A/G]ACACCCAAGAATGAT | 254065 |
rs79555791 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742439 | TTCTGTGAAGAAAGT[C/T]ATTGGTAGCTTGATG | 254065 |
rs79752371 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80770405 | AAATGTATCCAACAC[A/G]ATTAAGTTGGCTTTA | 254065 |
rs79794839 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80726329 | GTATAACATATAACA[C/T]GTTTACATGTTATGT | 254065 |
rs79890453 | snp | A/C | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80749116 | TGCTTTGTGTCCTAA[A/C]ATACGATCTATCCTG | 254065 |
rs79958326 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80713055 | GCCAGCTGCCCCGTC[C/T]GGGAGGGAGTTGGGG | 254065 |
rs80056240 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80770465 | CACAAATCAATAATC[A/G]TAATCCATCACACAA | 254065 |
rs111301170 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80708634 | CAGCCTGGCCAACAG[A/G]GTGAAACCCTGGCTC | 254065 |
rs111303810 | snp | A/T | 0.0384368 | 0.133195 | intron-variant | BRWD3 | GRCh38.p7 | X:80760315 | TTCTCAACATCAATT[A/T]TAAGTGCTAATGAAC | 254065 |
rs111320610 | snp | A/G | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80723691 | AGGGCTTTAAACAAA[A/G]TTTGTGAATGACACA | 254065 |
rs111519017 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742586 | ATTGAGCAGTGGTTT[A/G]CAGTTCTCCTTGAAG | 254065 |
rs111532866 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789429 | CGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 254065 |
rs111563543 | snp | A/G | 0.0204488 | 0.0990265 | intron-variant | BRWD3 | GRCh38.p7 | X:80722393 | GGTGAGATAAACGAT[A/G]AAAAAGTACTATGCT | 254065 |
rs111621947 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80722656 | TGTGGGATGAGGATT[C/T]CCATCAACATCCACC | 254065 |
rs111633507 | in-del | -/ACTT | 0.00649535 | 0.056617 | intron-variant | BRWD3 | GRCh38.p7 | X:80727721 | AATCAAGGAGTTGAC[-/ACTT]CAAGTTGAGATTGGG | 254065 |
rs111676150 | snp | A/G | 0.0787474 | 0.182133 | intron-variant | BRWD3 | GRCh38.p7 | X:80692665 | GCAATTCTTGTCTAA[A/G]GTAGAAATAGTTAAT | 254065 |
rs111681008 | snp | A/C | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80790484 | TCCCCAAATAACATG[A/C]CAGATTTAAAATGAA | 254065 |
rs111721154 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80808870 | GCCCCTTTTGAGGGA[A/G]GAAGCCAATTCACCC | 254065 |
rs111755042 | snp | C/T | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80783623 | AGATATCTGCACTCC[C/T]ATGTCTATTGCAGTA | 254065 |
rs111844923 | snp | C/T | 0.0173306 | 0.0914601 | intron-variant | BRWD3 | GRCh38.p7 | X:80786184 | TGCTGAATGTCAAAT[C/T]ACTTAAAATTAAATA | 254065 |
rs111907783 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80805803 | AGCTGGGCGTGGTGG[C/T]GCGTGCCTGTAGTCC | 254065 |
rs111931781 | snp | G/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80722228 | CCAATACGATAAGCA[G/T]TGGAATTCCATCAGT | 254065 |
rs111965219 | in-del | -/CAA | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80735841 | CCTAAAATCTCTTAA[-/CAA]CCTATTGAAGTAGGT | 254065 |
rs112079566 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80737561 | TTAATCTGGCTGGGC[A/G]CAGTGGCTCACACCT | 254065 |
rs112099990 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705266 | GTGAGACTCCATCTC[A/G]AAAAAAAAAAAAAAT | 254065 |
rs112186701 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | BRWD3 | GRCh38.p7 | X:80684878 | ACTCAGTATTAGATC[C/T]CTTATTGTATTTAGA | 254065 |
rs112239932 | snp | A/C | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80728995 | CAAAATTTCTCCAGG[A/C]GTATACAACTGTTTA | 254065 |
rs112328850 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80769090 | CACCCAGATTCATAA[A/G]GCAAGTCCTTAGAGA | 254065 |
rs112341267 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80729723 | AATATCAAATGAATC[A/G]GCAATGTTCCTGTCA | 254065 |
rs112450203 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80744666 | TTTCTCAGTAAACAT[A/G]AGGCTACCCGTTAAT | 254065 |
rs112464363 | snp | C/G | 0.444386 | 0.157208 | intron-variant | BRWD3 | GRCh38.p7 | X:80767936 | TACGTGACGCATGCA[C/G]AAGCTTCAATAGCCG | 254065 |
rs112501161 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682544 | TTCTCCTCTTCTGAC[C/T]CTGGATTGCTGACTT | 254065 |
rs112614608 | snp | A/G | 0.0425 | 0.139441 | intron-variant | BRWD3 | GRCh38.p7 | X:80720294 | AGAGATAACAGCTCC[A/G]TATTGCCCCGGAAGA | 254065 |
rs112616001 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80743013 | TTTTTGTCCATTCAG[G/T]GTGATATTGGCTGTG | 254065 |
rs112622715 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80728660 | GGACTAGTATAGTAT[A/G]TCATAGAAAGGAACC | 254065 |
rs112715708 | snp | A/T | 0.0256233 | 0.11025 | intron-variant | BRWD3 | GRCh38.p7 | X:80740799 | CTAAGAATAAAAATG[A/T]CCCTCACATTAACCT | 254065 |
rs112804647 | snp | C/T | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80791787 | TGGTACCTATTTTTG[C/T]CTTCCTAATGAGTTC | 254065 |
rs112829587 | snp | C/T | 0.00105418 | 0.0229342 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744076 | CCTGAAGGACTGCAA[C/T]GGGTGCACAAGTTCG | 254065 |
rs112910521 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80779183 | AGCTGGGCGTGGTGG[C/T]GCATGCCTGCAATCC | 254065 |
rs112947262 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80789480 | TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 254065 |
rs113083494 | snp | A/G | | | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80723837 | TTCCATCTGGTGAAA[A/G]TTTACAATCAAACAC | 254065 |
rs113163510 | snp | A/T | | | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669061 | GCCCACTGGTAAACA[A/T]CTTTTTTGAAGGAGA | 254065 |
rs113209709 | snp | A/G | 0.0787474 | 0.182133 | intron-variant | BRWD3 | GRCh38.p7 | X:80679427 | CGAAGATAAGCAACC[A/G]AATATTTTTATTTTT | 254065 |
rs113232890 | snp | A/G | 0.5 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80719335 | ATCCACAAATGATGA[A/G]ATTATGAGACTTCAA | 254065 |
rs113241590 | snp | C/T | 0.0430067 | 0.140192 | intron-variant | BRWD3 | GRCh38.p7 | X:80692334 | GAAAACATGGTCCAT[C/T]GCTATGAAACTTAGA | 254065 |
rs113295382 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80734736 | AAAAAGGTTAACTAA[C/T]GTAGGATTCTTAGCA | 254065 |
rs113372641 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | BRWD3 | GRCh38.p7 | X:80768822 | CCAATCAGTGTGATG[C/T]ATTCAGGAGACCCAA | 254065 |
rs113391031 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80729393 | AACTAATGGAAAGAT[A/G]GTTGATTTCAGGACC | 254065 |
rs113401874 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80710235 | CACTTCCTGTGTCTT[C/G]TCTTGTATCTCTAAT | 254065 |
rs113630843 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80804492 | ATCCGCCTGCCTCAG[C/T]CTCTCAAAGTGCTGG | 254065 |
rs113696005 | snp | A/G | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80710074 | ATTGAAAAGGGCACC[A/G]TCGGAGCTTGCAGCT | 254065 |
rs113818779 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80787898 | GACCATCCTGACTAA[C/T]ACGGTGAAACCCTGT | 254065 |
rs113832830 | snp | G/T | 0.0389457 | 0.134 | intron-variant | BRWD3 | GRCh38.p7 | X:80682208 | TAGCTGGCCAAAGAA[G/T]AAATGCCCTAAAATT | 254065 |
rs113870104 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80744691 | GTTAATGATAATTTC[C/T]GGTAAAAATATATTA | 254065 |
rs116559809 | snp | C/T | 0.0580755 | 0.160203 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673126 | AATAACAGAAACGTA[C/T]TTAAAAGTATTAGAA | 254065 |
rs137853272 | snp | A/G | | | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677232 | GAGAAAAAAGAAACA[A/G]AAGAGAAATCTCATT | 254065 |
rs137903690 | snp | A/T | 0.0763124 | 0.179813 | intron-variant | BRWD3 | GRCh38.p7 | X:80790837 | TTCAATATATTAATT[A/T]TGACTAAAGCTTTAA | 254065 |
rs138140243 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80774820 | TTTCTATCACTACCA[A/T]CTCCACATTCATTTT | 254065 |
rs138216976 | snp | G/T | 0.0147244 | 0.0845304 | intron-variant | BRWD3 | GRCh38.p7 | X:80736734 | AGAGGACTACTACTA[G/T]GTCAGAAGGATCAAG | 254065 |
rs138240307 | snp | C/T | 0.000433384 | 0.0147141 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80682485 | TGCTCCACTACTAGA[C/T]AATGAACTGCTGCTG | 254065 |
rs138245412 | snp | A/G | 6.8433e-05 | 0.00584909 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717655 | TGGCCATCTGGCTCC[A/G]AGGAGCATTGTTATG | 254065 |
rs138280630 | snp | A/G | 0.0235569 | 0.105941 | intron-variant | BRWD3 | GRCh38.p7 | X:80724611 | TACAGTCACTGTTAC[A/G]ATTCATAAATCAGAA | 254065 |
rs138301385 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80714158 | AACCTATTTTCTCTG[A/T]AGTTTGCTACCTGGA | 254065 |
rs138343252 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80728029 | CATCCCTCTGATACA[C/T]AAACACCATGATATA | 254065 |
rs138411812 | snp | A/G | 0.01368 | 0.0815649 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811479 | TATATAATATTTTCA[A/G]TAACTTTGTGCACGA | 254065 |
rs138419403 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80706865 | CAAGACACCATCTCT[A/G]AAAGAATAGAAAATG | 254065 |
rs138550875 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80697817 | AGAACAATTTATATT[A/C]CTTTGGGTATATACC | 254065 |
rs138551066 | snp | A/G | 0.0520783 | 0.152732 | intron-variant | BRWD3 | GRCh38.p7 | X:80770547 | CCTTTGACAAAATTC[A/G]ACAACGCTTCATGCT | 254065 |
rs138572345 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766022 | TGTCAACTAGACTGG[G/T]TCACAGAATGCCCAA | 254065 |
rs138582490 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80728373 | TACTTCTTCCTCTTA[C/T]CCCTATTCCTTGAAA | 254065 |
rs138604361 | snp | C/T | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80758017 | CCAGCCTGACCAACA[C/T]GGTGAAACCCCGTCT | 254065 |
rs138848533 | snp | A/G | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80777219 | TTACTCCCAAGAAAG[A/G]TGAGTAACTCACTGA | 254065 |
rs138887408 | snp | C/G | 0.169101 | 0.236549 | intron-variant | BRWD3 | GRCh38.p7 | X:80741922 | TAGTTTAATTAGATC[C/G]CATTTGTCAATTCTG | 254065 |
rs138955137 | snp | C/G | 0.0292288 | 0.117303 | intron-variant | BRWD3 | GRCh38.p7 | X:80678024 | AACAGTGAGTAGTAG[C/G]AGATGAGTGCCAGTG | 254065 |
rs138999024 | snp | A/T | 6.84034e-05 | 0.00584782 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717590 | ACTAACCCCATTATT[A/T]AGTTCATTGACCACC | 254065 |
rs139037875 | snp | C/T | 0.000206645 | 0.0101627 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686932 | ATAAATGAGGCTCAA[C/T]AGTTCCTTGCATTGT | 254065 |
rs139071237 | snp | C/T | 0.00998887 | 0.0699618 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809303 | GATCAGGTAATACAG[C/T]TCTGGGGAAGAGGGG | 254065 |
rs139358289 | snp | A/C | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670868 | CTTTTTTCCTAAATG[A/C]ATTTTTTTTATTCTA | 254065 |
rs139359784 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80785250 | CAATTTTCTTCTTCT[G/T]ATTTAATTTTGGTAC | 254065 |
rs139370690 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80707910 | TAGAGAATAGATAAC[C/T]CGTGTACACAATCTC | 254065 |
rs139381903 | snp | A/G | 0.05658 | 0.158394 | intron-variant | BRWD3 | GRCh38.p7 | X:80772126 | TTACTGGGTATATAC[A/G]CAAAGGATTATAAAT | 254065 |
rs139393572 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80759299 | GCTGAGTTCACCATC[C/T]ATAGTTTCTAGAATC | 254065 |
rs139425833 | snp | A/C/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80694481 | TCCACCGACAACGTG[A/C/T]GCCGTGTGCCTGGAA | 254065 |
rs139447088 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80710360 | TTTTCCAAACCTGGT[C/T]ATCTGCTGACTATTT | 254065 |
rs139448124 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80725911 | ATGTTTACATATGTT[A/G]CATGCCTATATGACA | 254065 |
rs139550242 | snp | A/G | 0.0245906 | 0.108123 | intron-variant | BRWD3 | GRCh38.p7 | X:80772523 | CCTAATGTAAATGAC[A/G]AGTTTATGGGTGCAG | 254065 |
rs139592206 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80784222 | AATCAATTTCTGGTT[A/G]TTATAGGTACATAGT | 254065 |
rs139689017 | snp | C/G | 0.0115877 | 0.0752302 | intron-variant | BRWD3 | GRCh38.p7 | X:80744532 | AACTCACTTTTTAGT[C/G]ATTTGGCATTAAGTA | 254065 |
rs139723766 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80728676 | TCATAGAAAGGAACC[A/T]GGAACTTAAATTTCC | 254065 |
rs139745040 | snp | G/T | 0.0173306 | 0.0914601 | intron-variant | BRWD3 | GRCh38.p7 | X:80798552 | ATAATGGCTGACTCG[G/T]AACAGTTAAGTGCTC | 254065 |
rs139778993 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739517 | AGAGAAAGAGTATGA[C/T]AGAGAGGTCTACAGA | 254065 |
rs139800991 | snp | A/T | 4.56762e-05 | 0.0047787 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744233 | TGTAGCCCAAATTTT[A/T]ACTAAACAGTCATCT | 254065 |
rs139947756 | snp | C/T | 0.0699487 | 0.17344 | intron-variant | BRWD3 | GRCh38.p7 | X:80807424 | ATTTGCTTGCAATAA[C/T]ACTATATTTAAATTG | 254065 |
rs139989234 | snp | G/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80767993 | TTATCAGTGACTGAA[G/T]ATCAAATTAATGAAA | 254065 |
rs140006404 | snp | A/C | 0.0282 | 0.115346 | intron-variant | BRWD3 | GRCh38.p7 | X:80703013 | ATAAATATGGCTACA[A/C]TCATCAATCACAGAC | 254065 |
rs140124797 | snp | A/T | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80687498 | ATATAAAATAACTAC[A/T]TGTCTAATTATTATA | 254065 |
rs140140883 | in-del | -/AA | | | intron-variant | BRWD3 | GRCh38.p7 | X:80701571 | AGAGCGAGACTCGTC[-/AA]AAAAAAAAAAAAAAA | 254065 |
rs140194482 | snp | C/T | 0.0173306 | 0.0914601 | intron-variant | BRWD3 | GRCh38.p7 | X:80681114 | CACGCCTGGCCCCAT[C/T]TTACGTTTTAAGACT | 254065 |
rs140203774 | snp | C/T | 0.000188025 | 0.00969419 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80692096 | ATATTTACTTCCTTC[C/T]GGAATTGGCTCCATA | 254065 |
rs140235656 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80698229 | TAATCATACACATTT[A/C]CTGATTATTAATCAC | 254065 |
rs140294343 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80737347 | TAATACAATGTAAAT[A/G]CTGTAGTAATTTGTT | 254065 |
rs140310268 | snp | A/C | 0.0625469 | 0.165413 | intron-variant | BRWD3 | GRCh38.p7 | X:80764819 | AAACTCTTAAAGTTC[A/C]ACAATGAAATTAAAA | 254065 |
rs140333389 | snp | A/G | 2.3127e-05 | 0.00340044 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677234 | TGAGATTTCTCTTTT[A/G]TTTCTTTTTTCTCTT | 254065 |
rs140416572 | snp | A/G | 0.0358881 | 0.129059 | intron-variant | BRWD3 | GRCh38.p7 | X:80756366 | AATTAGCTGGGCCTG[A/G]TGGTGCATGCCTGTA | 254065 |
rs140429017 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729807 | AAACTTCATGTCTAC[A/T]ATTAACTTCAAACTA | 254065 |
rs140443912 | snp | C/T | 0.0358881 | 0.129059 | intron-variant | BRWD3 | GRCh38.p7 | X:80681634 | TCTAAGAAAATGATA[C/T]GAATATTTTGAGAAC | 254065 |
rs140464820 | snp | G/T | 4.56022e-05 | 0.00477483 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717626 | TCTGCTCCACGCCAT[G/T]AGATCTCTTTCAGTG | 254065 |
rs140516738 | snp | A/C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80747990 | ACTTCCTGTGCTACA[A/C/T]TGAATATAAGTGGCG | 254065 |
rs140522731 | snp | G/T | 0.0835963 | 0.186574 | intron-variant | BRWD3 | GRCh38.p7 | X:80727417 | AATTGTATCTGGGGA[G/T]AATCTGTTTCTGCTC | 254065 |
rs140636753 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80788293 | TGGGGGCAGGGAGGG[G/T]AGGAGACAACTGCAC | 254065 |
rs140713268 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80767123 | AAGCTTGAACTGGGC[A/G]GAGCCCACCTCAGCT | 254065 |
rs140766246 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | BRWD3 | GRCh38.p7 | X:80769248 | CAAGCAGACCTAATA[A/G]ACATCTACAGAACTC | 254065 |
rs140787435 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80754553 | CTATGTTGAATAGGA[A/G]TGAAAGCAGGCACTC | 254065 |
rs140806909 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80757369 | TTGTTAAGAATTTGC[A/C]ACTTATAAAAAACAA | 254065 |
rs140852252 | snp | A/G | 0.0162517 | 0.0886665 | BRWD3 | X | allele_origin=G(germline)/A(germline) | X:80676918 | CCTAGTGCCACCTCC[A/G]CCTCTTCCTCGACTC | 254065 |
rs140855074 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80760510 | ACACTGAATGGACTT[C/T]GAAAAAAGGCACAGG | 254065 |
rs140900106 | snp | C/T | 0.05658 | 0.158394 | intron-variant | BRWD3 | GRCh38.p7 | X:80697649 | CTGTTGTAAAGGCCA[C/T]GACCTCAATTTTTAT | 254065 |
rs140983203 | snp | A/C | 0.0131573 | 0.0800346 | intron-variant | BRWD3 | GRCh38.p7 | X:80701285 | AGGCACAGTGGCTCA[A/C]ACCTGTAATCCTAGT | 254065 |
rs141083110 | snp | A/G | 0.05658 | 0.158394 | intron-variant | BRWD3 | GRCh38.p7 | X:80763455 | CTTTTGTTGCTTTGG[A/G]AGATTTATGTTCTAG | 254065 |
rs141159570 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80742244 | GGCATTATGTCTGAG[G/T]GCTCTGTTCTGTTCC | 254065 |
rs141263475 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | BRWD3 | GRCh38.p7 | X:80734740 | AGGTTAACTAATGTA[A/G]GATTCTTAGCAGTAG | 254065 |
rs141496774 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80758922 | CACAGCTGTAATTTA[C/T]AGATACTTCTCTTTC | 254065 |
rs141609938 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant | BRWD3 | GRCh38.p7 | X:80687299 | TTTCCTCTACAACAT[C/T]AAGTTATAGAGCCTT | 254065 |
rs141611133 | snp | A/G | 0.0271702 | 0.113344 | intron-variant | BRWD3 | GRCh38.p7 | X:80696606 | TAGGAATTAAACTCT[A/G]GTCTTTATAATTCTA | 254065 |
rs141611900 | snp | A/C | 0.05658 | 0.158394 | intron-variant | BRWD3 | GRCh38.p7 | X:80758146 | GGAGGTTGTGGTGAG[A/C]CAAGATCGCGCCATT | 254065 |
rs141633116 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685183 | GCTGCAATACAGACA[C/T]AATTATATTGTGTAA | 254065 |
rs141681165 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80693608 | AACTAGAGTAAAGGT[C/T]ACTCATGCTATGCTA | 254065 |
rs141753929 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80721785 | CTTACCCTACACCCA[A/G]TAACTCTTTGCATTT | 254065 |
rs141897695 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80713962 | CTTTGGCATAGCATC[A/T]CATGACAGATAAAGA | 254065 |
rs141916492 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80708309 | GATGAGACAGGAGAA[C/T]TGCTTGAACTTGGGA | 254065 |
rs141921207 | snp | A/G | 0.01368 | 0.0815649 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811561 | TGGAATTTTCCATTT[A/G]TGGCATCATGTTGAC | 254065 |
rs141962222 | snp | C/T | 5.37447e-05 | 0.00518357 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80689830 | AAGTATCCAGTATAT[C/T]AGTACAGCTCTGATC | 254065 |
rs142026032 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80726125 | TCTGTATAACATATA[A/G]CACGTTTACATATGT | 254065 |
rs142085721 | snp | G/T | 0.0103709 | 0.0712593 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80744248 | TACTAAACAGTCATC[G/T]GAACCCTATAGTAAC | 254065 |
rs142110135 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80730131 | GAGGGGAATGTAAAA[C/T]GGTACAGTCACTTTG | 254065 |
rs142141091 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80704230 | TGGGCAACATAAGAC[A/C]CCATCTCTTTAAAAA | 254065 |
rs142180104 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | BRWD3 | GRCh38.p7 | X:80749078 | CTTAATATTATTTCA[A/G]TCTTCTTAAATTTGT | 254065 |
rs142210787 | snp | C/T | 0.000164505 | 0.00906781 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80735197 | TTTCACCGGGCGATC[C/T]CTAAAGATAAAAATA | 254065 |
rs142211225 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80725819 | ATGTGTTACATGCCT[A/G]TATAACATAACATGT | 254065 |
rs142223428 | snp | A/G | 4.74389e-05 | 0.00487003 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709553 | TCCTGCGTAAAGAAC[A/G]CCCACAGCTAGGCTC | 254065 |
rs142283513 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80747296 | CAAAGAATCATTCAA[A/G]GGAGAATATCAATAG | 254065 |
rs142314936 | snp | G/T | 0.0240739 | 0.107039 | intron-variant | BRWD3 | GRCh38.p7 | X:80741719 | TCTTCTTTTGAGAAG[G/T]GTCTCTTCATATCCT | 254065 |
rs142417044 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80739167 | GGTCATGAGAATTTG[A/C]CAGATTCTAGATACA | 254065 |
rs142470539 | snp | A/T | 0.0490645 | 0.148745 | intron-variant | BRWD3 | GRCh38.p7 | X:80690403 | AGTTTTCAGGGGAAG[A/T]GCCAAGAAGAGCAAG | 254065 |
rs142549993 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80773055 | TGTAACACAGATTAG[C/T]GATTGACAAGATGGG | 254065 |
rs142555243 | snp | A/G | 0.05658 | 0.158394 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670452 | CTTGGAAAAAAAATG[A/G]ATCCCCAGGCTGGAG | 254065 |
rs142580083 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725779 | TACATGTGTTACATG[C/T]CTATATAACGTATAA | 254065 |
rs142593537 | snp | A/C | 0.0520783 | 0.152732 | intron-variant | BRWD3 | GRCh38.p7 | X:80763179 | GAGTACTATTATTAT[A/C]TCCTTTTTAAATATG | 254065 |
rs142626919 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80697145 | CAAATTCTGTTTGGG[A/G]TATAGCTCGGTAATA | 254065 |
rs142819701 | snp | G/T | 0.0110639 | 0.0735497 | intron-variant | BRWD3 | GRCh38.p7 | X:80688294 | CAAACTTTCCCAATA[G/T]GCAGTGTACAAGCTG | 254065 |
rs142821340 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80799428 | ATATAGCAGAGAATA[C/T]GCTATTTGTTTTCCA | 254065 |
rs142836883 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80728237 | TGATAAACTGAAAAA[C/T]ATCAACACTACCCAT | 254065 |
rs142873460 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678278 | AAGGTTGAACTGATG[A/G]GACTTGCTGACAGAC | 254065 |
rs142937774 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80684669 | TTTAAATCAATGTGA[C/T]ACCTTTGCTTCATCG | 254065 |
rs142938137 | snp | C/T | 0.0276852 | 0.114351 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792749 | TAGGCATCTTTAATG[C/T]CTAATTTTACATTTT | 254065 |
rs143014892 | snp | A/G | 0.0353775 | 0.128208 | intron-variant | BRWD3 | GRCh38.p7 | X:80701364 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 254065 |
rs143041103 | snp | C/G | 0.0709308 | 0.174454 | intron-variant | BRWD3 | GRCh38.p7 | X:80693381 | TAAATGCAGTTGATT[C/G]TTCTATCTTGCTTTT | 254065 |
rs143090181 | snp | A/C | 4.60199e-05 | 0.00479665 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676940 | CCTCGACTCCCTCGT[A/C]CCCTGCCTCCTCTTC | 254065 |
rs143148561 | snp | C/T | 0.0495675 | 0.149422 | intron-variant | BRWD3 | GRCh38.p7 | X:80795905 | CACTGCACTCCAGCC[C/T]GTGGGTGACCCTGTC | 254065 |
rs143287451 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80734626 | GATGGTGTGACAGAT[A/G]CAGACCAATGTGAAT | 254065 |
rs143292097 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80707996 | TACTCTAGCATTAGT[C/T]TGATGCACAATATGA | 254065 |
rs143326764 | snp | G/T | 0.0131573 | 0.0800346 | intron-variant | BRWD3 | GRCh38.p7 | X:80771917 | TCAAAACCACAGTGA[G/T]ATACCATCTCACACC | 254065 |
rs143392049 | snp | C/G | 0.0709308 | 0.174454 | intron-variant | BRWD3 | GRCh38.p7 | X:80726716 | TGGACAAAAATACAC[C/G]TTGCTGAAAGAAAAT | 254065 |
rs143465445 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749534 | GATTCCATTTGTATG[G/T]AACATATTTTCCATC | 254065 |
rs143473906 | snp | A/G | 0.16651 | 0.235647 | intron-variant | BRWD3 | GRCh38.p7 | X:80768098 | AAAGACCAAATCTAC[A/G]TCTGATTAGTGTACC | 254065 |
rs143565380 | snp | A/G | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80741425 | TTTGGGTATATACCC[A/G]GTAATGGGATGGCTG | 254065 |
rs143571459 | snp | A/G | 2.29155e-05 | 0.00338486 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709446 | TGAAGAACTGTCTGA[A/G]TCTTCCTGTACACCT | 254065 |
rs143707694 | snp | C/T | 0.0640323 | 0.167081 | intron-variant | BRWD3 | GRCh38.p7 | X:80736910 | ATGTCAGTGAGTTTT[C/T]AAAATCCCAAATGAA | 254065 |
rs143816515 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80781885 | AGGAAAGATATTCCA[C/T]ATTCATGAATTATAA | 254065 |
rs143824970 | snp | C/T | 0.000290272 | 0.0120437 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80684155 | GTATCTATAACATCT[C/T]GATAATCCTACAAAG | 254065 |
rs143882866 | snp | A/T | 0.0126344 | 0.0784702 | intron-variant | BRWD3 | GRCh38.p7 | X:80681580 | CTTTTTGAAACCATA[A/T]CTCTGTTATTTTATT | 254065 |
rs143902101 | snp | A/G | 7.19209e-05 | 0.00599627 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80696804 | TGCAAGCTTCAAGCA[A/G]CACAGTGTGGGTGGG | 254065 |
rs143952486 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80679202 | GACTAATACTTCAGG[C/T]TGGAGACTAAGGTGA | 254065 |
rs144011467 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80725803 | CGTATAACATGTTTA[C/T]ATGTGTTACATGCCT | 254065 |
rs144013686 | snp | A/C | 0.0199298 | 0.0978146 | intron-variant | BRWD3 | GRCh38.p7 | X:80767648 | ACCAGAGAGAAAATT[A/C]TAAAAACCAGAGAGC | 254065 |
rs144015236 | snp | C/T | 2.28804e-05 | 0.00338226 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676838 | TCATCATCTGCAATA[C/T]GTGCTCGTTTGGCTC | 254065 |
rs144073655 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80718164 | TAAAACATCAATAAA[A/G]CTTTCAAAAATGTTA | 254065 |
rs144145082 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | BRWD3 | GRCh38.p7 | X:80710391 | TGACTACAGAGCTAC[A/G]TCCACTGGGGCCCAT | 254065 |
rs144213059 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80715366 | TCTGTTTATCAATTA[C/T]GGAAAAAAATGCAAA | 254065 |
rs144494984 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80740481 | AGTGCAGTGGCTCAC[A/G]TGCCTGTAATCCCAG | 254065 |
rs144500810 | snp | A/T | 0.0152462 | 0.0859689 | intron-variant | BRWD3 | GRCh38.p7 | X:80738529 | GCCAATACACAAATA[A/T]TAAAGAACATGTAAA | 254065 |
rs144575896 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80757722 | TCAATGATAGACCGT[A/G]CTTCTTAAATATTCA | 254065 |
rs144610382 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80728497 | ACTTATATGTCCTCA[C/T]TGTATACAATAACAT | 254065 |
rs144713971 | snp | A/T | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80690702 | AACTAAATCTAATTA[A/T]CTCTGACCAAATTCT | 254065 |
rs144714021 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80760955 | GGGAGGCTGAGGTGG[C/G]AGGATCCCTTGAGCC | 254065 |
rs144840583 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687696 | TTTCCTTCTGGGAAT[C/G]TGGAATCTTAGTACG | 254065 |
rs144885469 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80772363 | CTGAGCAAACTATCA[C/T]AAGGACAGAAAACCG | 254065 |
rs145117753 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80720338 | CAAGCAAGATGTGGA[A/G]GTAGAAGACAGGGAT | 254065 |
rs145119587 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80784299 | TTTATAAAAACTGTT[C/T]AGATTATGATAATTA | 254065 |
rs145208954 | snp | G/T | 0.01368 | 0.0815649 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810417 | ACAATATAAGCCCCG[G/T]ACTTTGGACTGGTAA | 254065 |
rs145334967 | snp | C/G | 0.0256233 | 0.11025 | intron-variant | BRWD3 | GRCh38.p7 | X:80726320 | GTTATGTCTGTATAA[C/G]ATATAACATGTTTAC | 254065 |
rs145447791 | snp | C/T | 0.0655152 | 0.168717 | intron-variant | BRWD3 | GRCh38.p7 | X:80719781 | ACGTAAAATAAAGTA[C/T]ATATCAAATGAAACA | 254065 |
rs145455281 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80696565 | ACACACACACACACA[A/C]ATATAAATAAAACGG | 254065 |
rs145526845 | snp | C/T | 0.000174071 | 0.00932765 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707444 | GGAAGAACTTTCACT[C/T]TGCCATTCAACAACA | 254065 |
rs145577851 | snp | A/G | 0.165644 | 0.235338 | intron-variant | BRWD3 | GRCh38.p7 | X:80726252 | GTTATATGTCTGTAT[A/G]ACATATAACACGTTT | 254065 |
rs145591463 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80761268 | CCAGTCAATCATATT[A/G]TCATCAAGGTCAGTA | 254065 |
rs145595667 | snp | G/T | 0.00211696 | 0.0324653 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810173 | TCCGGTGGAGGACCC[G/T]TCCCCCTGGGTTGAT | 254065 |
rs145697172 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80788804 | GAAATGACACGCATG[A/G]ATTTCAAAAGCACTG | 254065 |
rs145769170 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80740932 | TTTTAAATTATACTT[C/T]AAGTTTTAGAGTACA | 254065 |
rs145840708 | snp | C/T | 0.0110639 | 0.0735497 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80811129 | GTGAAGTGATAGGCT[C/T]ATCTTTGGTTGTTAT | 254065 |
rs145969897 | snp | C/T | 0.0302564 | 0.119217 | intron-variant | BRWD3 | GRCh38.p7 | X:80751126 | GGAAAGGGGAGATGC[C/T]GATCAAAGGGCACAA | 254065 |
rs145979609 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80742788 | TATCAGCTTAAGGAG[A/G]TTTTGGGCTGAGACG | 254065 |
rs146034263 | snp | G/T | 0.0495675 | 0.149422 | intron-variant | BRWD3 | GRCh38.p7 | X:80718252 | GAGCAACGAAAGAAA[G/T]AAAACAAAGTAACAG | 254065 |
rs146155363 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80746581 | TCATCTTCCCTTATA[C/T]ACTAAAAGTGCTTAA | 254065 |
rs146169033 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | BRWD3 | GRCh38.p7 | X:80741898 | TTCTTTTGCTGTGCA[A/G]AAGCTCTTTAGTTTA | 254065 |
rs146207659 | snp | C/T | 4.57033e-05 | 0.00478012 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80716218 | AGACTGATTTCTATG[C/T]CACCTTTTGCAGTTC | 254065 |
rs146212014 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | BRWD3 | GRCh38.p7 | X:80693688 | CTTGAACTTGAGAGA[A/G]ATGATTTAGGGTATC | 254065 |
rs146277699 | snp | G/T | 0.166077 | 0.235493 | intron-variant | BRWD3 | GRCh38.p7 | X:80772034 | GGGAGTGTAAACTAG[G/T]TCAACCATTCTGGAA | 254065 |
rs146297684 | snp | A/T | 2.5547e-05 | 0.00357391 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80685474 | TACCTCAGAAAGAGA[A/T]GAATCTTGTTGTCTT | 254065 |
rs146334108 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | BRWD3 | GRCh38.p7 | X:80724036 | CTGATACAGTAAATC[C/T]CTGAAAGAAATTAGG | 254065 |
rs146398839 | snp | A/G | 0.0204488 | 0.0990265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798121 | TTAAATAAATAAATA[A/G]ATAAATAAAATATGA | 254065 |
rs146413988 | snp | C/T | 0.000137382 | 0.00828685 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703575 | TAGGCTCACCTGCTA[C/T]AGAAACCAGTCCTCC | 254065 |
rs146425236 | snp | A/C | 0.00181659 | 0.0300832 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80676888 | ACCTCTTCCTCCTCT[A/C]CCTCTTCCCCTCCCC | 254065 |
rs146543142 | snp | C/T | 0.0115877 | 0.0752302 | intron-variant | BRWD3 | GRCh38.p7 | X:80733198 | AATGGAACACTTGAC[C/T]GACGTGGGTGCTAAC | 254065 |
rs146560442 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80740624 | TGTGGTGGCGCATGC[C/T]GGTAGTACCAGCTAC | 254065 |
rs146598410 | snp | A/C | 0.0271702 | 0.113344 | intron-variant | BRWD3 | GRCh38.p7 | X:80680455 | TAAATGCAGAAGGTT[A/C]TTCTGAGAATGCCTG | 254065 |
rs146660256 | snp | C/G | 0.0714214 | 0.174956 | intron-variant | BRWD3 | GRCh38.p7 | X:80764595 | TGGGATTACAGGTGT[C/G]AGCCACCGCGCCCAG | 254065 |
rs146694238 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | BRWD3 | GRCh38.p7 | X:80773242 | ATGAGTACAAGTAAA[A/G]CTGAGGACATCTGAT | 254065 |
rs146703990 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80707266 | GACGTCAGAAAGGTA[C/T]TGGGAGAGCCAGGAT | 254065 |
rs146779779 | snp | A/G | 0.0560809 | 0.157783 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672822 | TTTAAAAGGCTGGAC[A/G]GCAAAGTATACTGAA | 254065 |
rs146822367 | snp | A/C | 0.0147244 | 0.0845304 | intron-variant | BRWD3 | GRCh38.p7 | X:80711820 | CCATGAGTTGTCCTG[A/C]CTTTCTGTACTAAAC | 254065 |
rs146864652 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80794228 | TATGGAATCAGAGCC[A/G]GGTGCAGTAGCTCAG | 254065 |
rs146883672 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80733004 | GTGTGGTGGCATGCA[C/T]CTGTAATCCCAGCTA | 254065 |
rs147010580 | snp | C/T | 0.101293 | 0.200963 | intron-variant | BRWD3 | GRCh38.p7 | X:80796255 | CCTGCCTCAGCCTCA[C/T]GAGTAGCTGGGATTA | 254065 |
rs147077762 | snp | C/T | 0.0374181 | 0.131563 | intron-variant | BRWD3 | GRCh38.p7 | X:80722407 | TGAAAAAGTACTATG[C/T]TAAGGTAAAAACAAC | 254065 |
rs147113308 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714108 | GAATCAACTAAGAGT[C/G]TGGCATCTTTTTAAG | 254065 |
rs147256791 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80766912 | CATTCGCACCCAAAT[A/T]CTGTGCTTTCCCAAC | 254065 |
rs147362505 | snp | G/T | 0.0168099 | 0.0901243 | intron-variant | BRWD3 | GRCh38.p7 | X:80790660 | GAGAGAAGGGAAGAA[G/T]GGATAAAGAAAGCCT | 254065 |
rs147449377 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80702335 | AAGAGGAATTCCACC[A/G]AAGAATGGAGAAAAA | 254065 |
rs147617562 | snp | A/G | 2.29658e-05 | 0.00338857 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709505 | GCTCTATGTTGGACC[A/G]TGTTTGGTAAGTATG | 254065 |
rs147647069 | snp | C/T | 0.0714214 | 0.174956 | intron-variant | BRWD3 | GRCh38.p7 | X:80801122 | TATCTATATATATCA[C/T]GCTTCTAAAAAAAGT | 254065 |
rs147681411 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748870 | ATAAACTTACCTCTC[C/T]GGGCTGTTTTTGCTG | 254065 |
rs147698046 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80754355 | TTGTACTTTGATTTT[A/G]TAACCTGAAACTTTA | 254065 |
rs147906328 | snp | C/T | 0.00491173 | 0.0493127 | intron-variant | BRWD3 | GRCh38.p7 | X:80696032 | ATCAATATAGAGATA[C/T]AACAATATATGTTAC | 254065 |
rs147907793 | snp | A/G | 0.0714214 | 0.174956 | intron-variant | BRWD3 | GRCh38.p7 | X:80806751 | ACCATTAAAATAATG[A/G]TGACTATTCAAATAC | 254065 |
rs147925519 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80781598 | GTAGGGGTCGTGCAG[C/T]TGAGATTTCCTCGGG | 254065 |
rs147941911 | snp | A/C | 0.0026483 | 0.0362924 | intron-variant | BRWD3 | GRCh38.p7 | X:80721315 | CTTTCTTATTCATTT[A/C]TTTTCAAGTTTATCT | 254065 |
rs147979636 | snp | A/G | 0.0240739 | 0.107039 | intron-variant | BRWD3 | GRCh38.p7 | X:80749656 | CTCAATGTCAAAAAT[A/G]TCCATTCTACCCAAC | 254065 |
rs148000516 | in-del | -/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761535 | TTATACTAAACTTAA[-/G]GTTTAATATTTTACA | 254065 |
rs148045997 | snp | C/T | 0.0068637 | 0.0581785 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673865 | GTACTTGCTTTGCTA[C/T]GGCTGGACCCAGATT | 254065 |
rs148103495 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80788919 | CAGTCACAGAAAGAT[C/T]AGTGGTTTCCAGGGG | 254065 |
rs148137719 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80700882 | ATAGGAGGATGTACA[C/T]AGGTTATATGCAAAT | 254065 |
rs148170741 | snp | A/T | 0.0185201 | 0.0944301 | intron-variant | BRWD3 | GRCh38.p7 | X:80722833 | ACACAGGGAATTTAT[A/T]AGTAAATACTTGTTT | 254065 |
rs148332560 | snp | C/T | 2.31795e-05 | 0.0034043 | intron-variant | BRWD3 | GRCh38.p7 | X:80716139 | GTGTATCCCAAAGTA[C/T]TGTAAAACTATACTT | 254065 |
rs148455647 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | BRWD3 | GRCh38.p7 | X:80761924 | TTTGACTCAACCACA[C/T]GAAGACACATTTGCC | 254065 |
rs148491212 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80778404 | TGGAGGTGCAGTGGG[G/T]GATGAAGCAAGGAGA | 254065 |
rs148556531 | snp | A/G | 0.000251572 | 0.0112126 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80688096 | TGAAGTACCAGGACC[A/G]TCTGAATCTAAATCA | 254065 |
rs148682378 | snp | A/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80783829 | GCCAAGCACAGAAAG[A/T]CAAACTTTACATCTT | 254065 |
rs148787836 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80746637 | AAACATAGGCTCCCT[A/G]TAACTTCAAAGGTCA | 254065 |
rs148827537 | snp | C/T | 0.00633741 | 0.0559334 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810240 | CCTTTCCCCTTTTTC[C/T]TCCCGGTACCAAAGC | 254065 |
rs148875743 | snp | A/G | 0.000146149 | 0.00854711 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707477 | ATCCTCTACCGAAGC[A/G]TCACTTGTGCCAACA | 254065 |
rs148897706 | snp | A/G | 0.0183711 | 0.0940641 | intron-variant | BRWD3 | GRCh38.p7 | X:80749305 | TATTGCAGTTGCAGT[A/G]TCTCTCTCTCTCTTC | 254065 |
rs148947693 | snp | A/G | 0.0615552 | 0.164282 | intron-variant | BRWD3 | GRCh38.p7 | X:80741378 | TAAACATCTGTGTGC[A/G]TGTGTCTTTAGAGCA | 254065 |
rs149017241 | snp | C/G | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80781685 | ATATAAGCATGCATA[C/G]AAAAATCAGTAGCAT | 254065 |
rs149070728 | snp | A/G | 0.0152462 | 0.0859689 | intron-variant | BRWD3 | GRCh38.p7 | X:80772485 | GGGTGGAGGCCAGGG[A/G]AGGGATAGCATTAGG | 254065 |
rs149103817 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80692734 | TTAGTTATTCCTTTG[C/T]TTTAGTCAAAGAAAA | 254065 |
rs149158313 | snp | C/T | 0.0307697 | 0.120159 | intron-variant | BRWD3 | GRCh38.p7 | X:80795360 | ATATATATACACACA[C/T]ACACACATGTGTATA | 254065 |
rs149212729 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | BRWD3 | GRCh38.p7 | X:80786943 | TTTGCAGACAACAGG[A/G]TTATCTATATAAAGA | 254065 |
rs149269089 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80797713 | GACTTGTACAATAAA[C/G]AAGTTTGACTTTCAC | 254065 |
rs149335661 | snp | C/T | 0.0704399 | 0.173949 | intron-variant | BRWD3 | GRCh38.p7 | X:80728445 | CCCCTATAACGGTAA[C/T]AATGAAAAAATGCCA | 254065 |
rs149370074 | snp | C/T | 0.00018818 | 0.00969817 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80686993 | GACTGTCTTCTGCCT[C/T]GGCATTTGACCTACA | 254065 |
rs149478535 | snp | A/T | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80700119 | ATATAACTCTGTATG[A/T]CCAATATACATTCCT | 254065 |
rs149496574 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80678763 | TTGAAAAGAAGACTA[A/G]GGCTGTAGATAATTA | 254065 |
rs149564749 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80714622 | ATAAAACCAAGTTGT[A/G]GCCCGACCATCTCAG | 254065 |
rs149612876 | snp | A/G | 0.000189982 | 0.00974449 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717690 | TGTCTAACACCTTCA[A/G]TTTGACTACTATGTC | 254065 |
rs149617660 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80706894 | TGAAATGAAGAAACC[A/G]TAATAATATAAAAGT | 254065 |
rs149638650 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | BRWD3 | GRCh38.p7 | X:80804640 | AATATATAAAACTTA[C/T]AGATTAACAAGAACT | 254065 |
rs149688283 | snp | C/T | 0.00012636 | 0.00794758 | missense, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80707437 | ACTACCTGGAAGAAC[C/T]TTCACTTTGCCATTC | 254065 |
rs149723008 | snp | G/T | 0.0570788 | 0.159001 | intron-variant | BRWD3 | GRCh38.p7 | X:80709899 | TCAGTTTTGCCAGAG[G/T]CTGCAACCAGACCTG | 254065 |
rs149797221 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80799874 | CTATCTACTAAAGTT[C/T]GGTTAGGACAAAGAC | 254065 |
rs149814437 | snp | A/C | 0.00791962 | 0.0624267 | intron-variant | BRWD3 | GRCh38.p7 | X:80730447 | AGAAAGAAAGAAAGA[A/C]AGACACAGTTAACAC | 254065 |
rs149847496 | snp | A/G | 0.0560809 | 0.157783 | intron-variant | BRWD3 | GRCh38.p7 | X:80753339 | CAGTGGTGTGATCTC[A/G]GCTCACTGCAACCTC | 254065 |
rs149886217 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80772168 | AAAGACACACGCACA[C/T]GTATGTTTATTGCGG | 254065 |
rs149975189 | snp | A/T | 0.343052 | 0.232037 | intron-variant | BRWD3 | GRCh38.p7 | X:80794528 | AAAAATAAATAAAAA[A/T]ATATATATATATCTC | 254065 |
rs150004766 | snp | C/G | 0.00415658 | 0.0453984 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80703586 | GCTATAGAAACCAGT[C/G]CTCCTTTCTAAAACA | 254065 |
rs150114170 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80706785 | CTGTACACCCTGCTA[C/T]GCAGGAGGCTGAGGT | 254065 |
rs150167508 | snp | C/G | 0.0105399 | 0.0718252 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810130 | CTCCGGAGTGACTTT[C/G]CCTTCCTGTGAAGGC | 254065 |
rs150338848 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80692494 | TAAAGTAGATGTTGA[A/C]AACAAATAGTACTTC | 254065 |
rs150376139 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80757297 | AACTCATTAAAACAG[A/G]GCAATCAATCAACAT | 254065 |
rs150411352 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80774524 | CATACTAATTACTGC[C/T]AATCTTTATCTGTAA | 254065 |
rs150423801 | snp | C/T | 2.28087e-05 | 0.00337695 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80717653 | AGTGGCCATCTGGCT[C/T]CGAGGAGCATTGTTA | 254065 |
rs150502079 | snp | C/T | 0.0550819 | 0.156547 | intron-variant | BRWD3 | GRCh38.p7 | X:80796991 | CTCGCCTGGTAAACA[C/T]AGCACCACCCTCATC | 254065 |
rs150522762 | snp | C/G | 0.0214859 | 0.101397 | intron-variant | BRWD3 | GRCh38.p7 | X:80780208 | TTCTATCTCTATAAA[C/G]TACTGAGTTAAACAT | 254065 |
rs150641668 | snp | A/G | 0.16521 | 0.235182 | intron-variant | BRWD3 | GRCh38.p7 | X:80708677 | AAAAATTAGCCATGC[A/G]TGGTGGCGCATGCCT | 254065 |
rs150663223 | snp | C/T | 0.0719118 | 0.175455 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792884 | TAACAATTACTGAGG[C/T]CCGGCGCAGTGGTTT | 254065 |
rs150692884 | snp | A/G | 0.000189982 | 0.00974448 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691055 | AAAAAAAACAGACCT[A/G]TAAAAGCGATTTTCA | 254065 |
rs150712224 | snp | A/G | 0.103655 | 0.20269 | intron-variant | BRWD3 | GRCh38.p7 | X:80743108 | TTTTTAGCATGAAGC[A/G]TTGTTGAATTTTGTC | 254065 |
rs150728684 | snp | A/G | 0.0266548 | 0.112325 | intron-variant | BRWD3 | GRCh38.p7 | X:80725906 | ATAACATGTTTACAT[A/G]TGTTACATGCCTATA | 254065 |
rs150742567 | snp | C/T | 5.24631e-05 | 0.00512141 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80809273 | GTTGCAGGGTCCAGA[C/T]TGCAAGAACCTAGCG | 254065 |
rs150870745 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80694433 | AGAGTTGTGAGAAGA[G/T]AGTCACCGTCCTCCA | 254065 |
rs150963716 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80769211 | TAACAAGGATATCCA[A/G]GAACTGAACTCAGCT | 254065 |
rs150977474 | snp | C/T | 0.0374181 | 0.131563 | intron-variant | BRWD3 | GRCh38.p7 | X:80697293 | GAAGACTTATATATT[C/T]TAATGTCTACAACAT | 254065 |
rs151030815 | snp | C/T | 0.0245906 | 0.108123 | intron-variant | BRWD3 | GRCh38.p7 | X:80689639 | TGGCTGAATACCAGC[C/T]TCTTTTAAAGTGTAC | 254065 |
rs151103792 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | BRWD3 | GRCh38.p7 | X:80782294 | GGTGCTAGGAAAATT[A/G]GATACCCATATGCAG | 254065 |
rs151174125 | snp | A/G | 0.0282 | 0.115346 | intron-variant | BRWD3 | GRCh38.p7 | X:80711097 | ATAGGATGAAGCAAG[A/G]CATTTCAGTCATATG | 254065 |
rs151186096 | snp | C/T | 6.84127e-05 | 0.00584822 | missense, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677112 | CATGGTCTCCATCTA[C/T]GTAATCTTGATCTGT | 254065 |
rs151191983 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80755913 | AAATGTATGGATAAG[C/G]ACCATAAAGAAACAA | 254065 |
rs151242341 | snp | A/G | 0.0251071 | 0.109193 | intron-variant | BRWD3 | GRCh38.p7 | X:80747806 | CATTACTCAATTTGT[A/G]TATCAGTTATAAGAG | 254065 |
rs151312076 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | BRWD3 | GRCh38.p7 | X:80785117 | TAATCTTTAAAATGA[C/T]GAAGAAATAGTAATA | 254065 |
rs151314177 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80727225 | AGACTCCTATAATCT[A/G]TCTGCAGTCACTCTT | 254065 |
rs180673717 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80715920 | ATGGTTATTTTAATA[C/T]AAATATCTTACACCT | 254065 |
rs180680148 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80694589 | CTGCCCAAGAGCATG[A/G]GAACTCACCTCTTGC | 254065 |
rs180685784 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736976 | GATTAAGATATATAG[G/T]GTTTGAATACATTTT | 254065 |
rs180710424 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752670 | ATGTTGAGCATTTTT[G/T]CTTTTTCTTTCTTTC | 254065 |
rs180710457 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | BRWD3 | GRCh38.p7 | X:80789399 | TCTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 254065 |
rs180723802 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80769458 | CAAAACCACAAAACT[A/G]CATGGAAACTGAACA | 254065 |
rs180819372 | snp | C/G | 0.0131573 | 0.0800346 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704277 | AGTGGAATGGAGGGA[C/G]AGTCCTATACAATTT | 254065 |
rs180829559 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680624 | ATTGACTGAAAGAAG[G/T]CTCATTTCTCAGCCC | 254065 |
rs180829946 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725991 | GTTATATGTCTATAT[A/G]ACATAACATGTTTAC | 254065 |
rs180875963 | snp | A/C | 0.0026455 | 0.0362733 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671276 | TTAAAGTGTAAACAT[A/C]ATATTTATTATCCTA | 254065 |
rs180892443 | snp | C/G | 0.0157677 | 0.0873799 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675017 | AGCCTGATCTAAGTG[C/G]AACAAATTTGCTGTT | 254065 |
rs180932617 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80689531 | AGTGTTGATTTCTCG[A/T]CACTTACATCCACTG | 254065 |
rs180949706 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80748171 | TCTATACCTCTTATG[C/T]TGAGATTTTATCATG | 254065 |
rs180952900 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80756468 | GATCGCACCATTGTA[C/T]GCCAGCCTGGGCAAC | 254065 |
rs180957893 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733202 | GAACACTTGACTGAC[A/G]TGGGTGCTAACAGAA | 254065 |
rs180962570 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80794184 | CTCTGACTCAAAAAA[A/G]GAAATAAAAAAAATA | 254065 |
rs180963828 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80699736 | TTTGCTCTAATTATG[A/G]ACTAGTATAGACTAG | 254065 |
rs180974863 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739873 | ATGTCATTGCACTGC[A/T]TTCACCTATTTTCAA | 254065 |
rs180992230 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80772125 | ATTACTGGGTATATA[C/T]GCAAAGGATTATAAA | 254065 |
rs181103770 | snp | A/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80778148 | AAACTCAAGAGTTGA[A/T]AAGTGCCTTGTTACC | 254065 |
rs181106492 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800348 | AAATCAAGACCAGCC[A/T]GGGCAAAAAAAAGTG | 254065 |
rs181192117 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80753713 | ATATGGTTAGAGATA[C/T]GGGTCCAGTTTTATT | 254065 |
rs181214540 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80789444 | GCAGTGGCGCGATCT[C/T]GGTTCACTGCAAGCT | 254065 |
rs181218968 | snp | A/C | 0.00844089 | 0.0644143 | intron-variant | BRWD3 | GRCh38.p7 | X:80769789 | AAAAACCTTCAAAAA[A/C]AAAAAATCAATGAAT | 254065 |
rs181284305 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807294 | ATCACAATTATACCA[C/T]TTTCTGTGATTTGCA | 254065 |
rs181300251 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80700227 | GTTAATTCAGTATTC[A/G]TGCCTACGTAGCCCT | 254065 |
rs181314295 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80722220 | CCAAAATACCAATAC[A/G]ATAAGCAGTGGAATT | 254065 |
rs181320670 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80757064 | TCCTAGCCTGATGTA[G/T]TCACTATAATGGCAT | 254065 |
rs181322192 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80740957 | AGTACATGTGCACAA[C/T]ATGCAGGTTTGTTAC | 254065 |
rs181374826 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80723185 | TGGTAAAACAGGTAA[A/G]TATCAATCACATCAA | 254065 |
rs181383213 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80741360 | TTGTGAATAGTACTG[A/C]AATAAACATCTGTGT | 254065 |
rs181401191 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80773701 | CTATCCTATGCAGGT[A/G]TCTTCTCACCTGGAA | 254065 |
rs181404213 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758154 | TGGTGAGCCAAGATC[A/G]CGCCATTGCACTCCA | 254065 |
rs181418434 | snp | C/T | 0.00320598 | 0.0399088 | intron-variant | BRWD3 | GRCh38.p7 | X:80795352 | AATTGTGTATATATA[C/T]ACACACACACACACA | 254065 |
rs181436167 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80785295 | TTGATTAGTCAAGCA[C/T]ACAGCTAATGAAATG | 254065 |
rs181441639 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80773112 | CGATGTGGTTATAAA[A/G]GAGTAACATGATGAA | 254065 |
rs181472149 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80732862 | AGAACAATGTTGGCC[A/G]GGCATGGTGGCTCAC | 254065 |
rs181488598 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80700496 | AATCCCAGCACTTTG[A/G]GAGGTTGAGGCAGGT | 254065 |
rs181496199 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80766676 | GAACAGCTCCGGTCT[A/G]CAGCTCCCAGCGTGA | 254065 |
rs181503173 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80805805 | CTGGGCGTGGTGGCG[C/T]GTGCCTGTAGTCCCA | 254065 |
rs181585318 | snp | A/T | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80794634 | TAAATATTTAATAAT[A/T]GACCAAATTTAAGAA | 254065 |
rs181597387 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80688386 | GGAACAGTGTAGTGG[C/T]TGGTATTTGCTAAAA | 254065 |
rs181602511 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80744921 | GGTGTAATAACTTCC[C/T]GAATAACTTCCACTT | 254065 |
rs181610263 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80737640 | GGGAGTTCGAAACGA[A/G]ACTGGCCGATATGGC | 254065 |
rs181617054 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80761960 | GTACAATTAGAAACA[A/T]TATTTCTACTCATTT | 254065 |
rs181617490 | snp | C/T | 2.27931e-05 | 0.0033758 | synonymous-codon, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80677059 | ATGTTGCTTTCTGAG[C/T]TTTCTTTTAGGTCTG | 254065 |
rs181622186 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80747829 | TATAAGAGGGTTCTT[C/T]TGGTGGATTTTTAGG | 254065 |
rs181632151 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783548 | AATAGGACTACCATA[C/T]AATTCAGTGATCCTA | 254065 |
rs181794447 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80681599 | TGTTATTTTATTCTA[A/G]CACCAAAATTATAAG | 254065 |
rs181806584 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726270 | ATATAACACGTTTAC[A/G]TGTTATGTCTGTATA | 254065 |
rs181855039 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80766742 | CAGAGGTAGCTGGTT[A/C]ATTTCTTTGGCACTG | 254065 |
rs181862870 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785046 | GCAGAACTGTCTGTG[C/T]GAAATTTTAACTTCA | 254065 |
rs181866914 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80806706 | TGGTTCAAATCATAT[C/T]GTACCTTAAATACAA | 254065 |
rs181871971 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711374 | TTAACCCTATATAAC[A/G]TGTTTTAACTTTCCA | 254065 |
rs182009257 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80693918 | AATTCAAGCCAGCTG[C/T]AGAAATTTGCATAAG | 254065 |
rs182020220 | snp | C/T | 0.022522 | 0.1037 | intron-variant | BRWD3 | GRCh38.p7 | X:80683739 | CTGTCAATCACCTTT[C/T]TATTTATTAAGTCAC | 254065 |
rs182023137 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715414 | AGATTTGTTTAACAA[C/T]ATCAAAATCATCCTA | 254065 |
rs182035315 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752445 | GCTGGATTGAATGGA[C/T]ATTCTATTTTTAGTT | 254065 |
rs182036610 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80736623 | AGATGTAAGCCATTT[C/G]TTTCCATAAATAATG | 254065 |
rs182042927 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80768746 | TATTAACCTTAAATG[C/T]AAATGGGCTAAATGC | 254065 |
rs182051117 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80705122 | AATACAAAAATTAGC[C/T]GGGTGTGATGGCACA | 254065 |
rs182055997 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788705 | TAGCTTTATCCATAA[C/T]AGGCAAAATTATTGA | 254065 |
rs182096690 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80685079 | ATATTCTAACACAGT[A/G]TGGCTTATGTTAGAA | 254065 |
rs182113162 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80727175 | CACCACCACACAAAT[A/C]TAAATTATCATCCTG | 254065 |
rs182120425 | snp | G/T | 0.00265181 | 0.0363163 | intron-variant | BRWD3 | GRCh38.p7 | X:80706584 | TTTTCCTGTTCAACG[G/T]AAGGTATTCAGAGAC | 254065 |
rs182139505 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80781084 | GTCCTGAGCTGTATA[C/T]AGTGTAAATTACAAG | 254065 |
rs182142162 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762491 | TAATGGATCTAAAGC[A/G]GTGAACTCCTCCTCA | 254065 |
rs182219891 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670575 | ACACACAACCATGCC[C/T]AGCTAATTAAAAAAA | 254065 |
rs182258070 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80705991 | ATATTTTTCTTTCTT[C/T]AACAAGAAATTAATC | 254065 |
rs182310913 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80745464 | TTCTGCACCCATATA[A/T]CCAAAAAAAGTGAAC | 254065 |
rs182326052 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80779223 | AGGAGGCTAAGGCAG[A/G]AGAATCGCTTGAACC | 254065 |
rs182400877 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80697454 | ACAAATAGCTAAGTT[C/T]TTAACCCCTATCCCC | 254065 |
rs182414928 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738476 | AAAAAAAATACAAAA[C/T]GTGGGAGAATAATAT | 254065 |
rs182445168 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80801872 | ATAATATATAGAAAA[C/T]AAATTCAGGATACAA | 254065 |
rs182449402 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80771083 | GAGAACTACAAACCT[A/G]CTCAGCGAAATAAAG | 254065 |
rs182557190 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80726364 | ATAACATATAACATG[A/T]TTACATGTTATATCT | 254065 |
rs182566812 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80762282 | TAAATTCTTAATGCA[A/G]CTTCTCATTTTACAT | 254065 |
rs182596196 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80800858 | AATCATTATGCATAG[C/T]ATTTCTTTTTCTTTT | 254065 |
rs182607627 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80762816 | TCTAAGAATTAAATG[A/C]GGTGAATTTTGTAGA | 254065 |
rs182621393 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80781306 | TGTGCTCTCAGGCGA[C/T]AGATGAGTGGCTATT | 254065 |
rs182634498 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80802528 | AAATATAACATCTGG[G/T]GTCATAGTTCTCCAG | 254065 |
rs182653150 | snp | A/G | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673496 | GTGTCAAGTTGGGGA[A/G]AAAACTTTACACACA | 254065 |
rs182666983 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80678450 | TTAGATGTTGACAGA[G/T]ATCCAAGACAAGACA | 254065 |
rs182667330 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80719281 | GACAGTGTATTAAAA[C/T]GCATCACCTGTATTT | 254065 |
rs182685916 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759948 | CCACATTTTGGTCTA[C/T]AGATTCCTAAATGCA | 254065 |
rs182686970 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80775278 | AGGATGTAGAATAAT[C/T]GGGCCCCTACCTCCC | 254065 |
rs182687326 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754694 | TTCTATGCCCAATTT[G/T]TTGAGGATTTTTACC | 254065 |
rs182698315 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80790882 | TGGAAAATTCTGGTG[C/G]ATAAACAAACAACTC | 254065 |
rs182750390 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80713663 | CCAAATCCCCCTCTG[C/T]GAGAGACACCCAAGA | 254065 |
rs182818504 | snp | C/T | 0 | 0 | intron-variant | BRWD3 | GRCh38.p7 | X:80702166 | CAATTATATAAAAAG[C/T]GTATGTTTGCCTTTA | 254065 |
rs182833269 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80724517 | TCTTAAAGAACATCC[A/G]TATCTCCAAGTCCAT | 254065 |
rs182851363 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80742509 | GCCATTTTCACGATA[C/T]TGATTCTTCCTACCC | 254065 |
rs182908963 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80729163 | TTGAGAACCAAAAAC[G/T]ACTAAGAAATCTATA | 254065 |
rs182938865 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776063 | TTCCCACTTTTCAAT[A/G]TTGTCTATTTAATGA | 254065 |
rs182940963 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798324 | GCTTACTTGAATCTG[C/T]TTGCTTTTCATTAAA | 254065 |
rs182943546 | snp | C/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80701829 | ACTGATCATTGAACA[C/T]CTATGTGTAGGCACT | 254065 |
rs182952484 | snp | C/T | 0.000496481 | 0.0157478 | synonymous-codon, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80695975 | GAAGTCAATGACATC[C/T]GGCATGTCATGATAC | 254065 |
rs182966934 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80717284 | TTTAATTATGTAAGA[C/T]CTCATGAGTTCTTAA | 254065 |
rs183157250 | snp | C/T | 2.57036e-05 | 0.00358485 | missense, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80691936 | GCAGTCAATTCTTCC[C/T]GGGAGACAGGAACAC | 254065 |
rs183166562 | snp | A/G | 0.100346 | 0.200259 | intron-variant | BRWD3 | GRCh38.p7 | X:80713451 | TTAAATGGATTAAGG[A/G]CGGTGCAAGATGTGC | 254065 |
rs183169667 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714040 | AAATAGCCCTGCAAA[C/G]TTGTCTCTTGTGGGG | 254065 |
rs183175854 | snp | A/G | 2.84341e-05 | 0.00377045 | intron-variant | BRWD3 | GRCh38.p7 | X:80707410 | AATTTTGACCAAATT[A/G]AAACCATTAAAACTA | 254065 |
rs183176178 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80750468 | TGGCCAATGGATATA[C/T]GAAAAAATGCTCAAC | 254065 |
rs183178686 | snp | A/T | 0.000166144 | 0.00911288 | intron-variant | BRWD3 | GRCh38.p7 | X:80735213 | CTAAAGATAAAAATA[A/T]GGTGTTTTTGTGTTT | 254065 |
rs183183900 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80767694 | GGATTGCAGCTCCTC[A/G]CCAGCAACAGAACAA | 254065 |
rs183186207 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80745950 | CCCAAGGGACTGATA[C/T]TCTGCTTGGCTTACT | 254065 |
rs183200635 | snp | C/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80809911 | GGCAAAGGGGGTGGA[C/G]AGAGGGGAGGGTAAA | 254065 |
rs183212077 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748552 | AGACTTTTTATTACC[A/G]ACTCAATCTCATTAC | 254065 |
rs183236700 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80790546 | TTCCTAAGCAATTAC[C/T]AAAAGAATAACAAAC | 254065 |
rs183261230 | snp | A/T | 2.28136e-05 | 0.00337732 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80734168 | CCTCAGAACCCAAAT[A/T]ATATATTCTAATCAC | 254065 |
rs183288655 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | BRWD3 | GRCh38.p7 | X:80797738 | TTTCACTCTATACAA[C/T]AGAAAATTGCTCGAT | 254065 |
rs183307141 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80766928 | CTGTGCTTTCCCAAC[A/G]GTCTTAGCAAATGGC | 254065 |
rs183317709 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80808747 | GCTATTGGCTCAGAG[A/C]TAGACAAGTATATGG | 254065 |
rs183428806 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80690887 | TCTATCCCCAAGAGT[A/G]AGAATCTACTAAATA | 254065 |
rs183430665 | snp | G/T | 4.58542e-05 | 0.00478801 | intron-variant | BRWD3 | GRCh38.p7 | X:80717537 | CCTAAGAATAAAGCT[G/T]TAAATTTTTTTCTAA | 254065 |
rs183435458 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | BRWD3 | GRCh38.p7 | X:80708801 | AGCCTGGGGACAGAG[G/T]GAGACTCCATCTCAA | 254065 |
rs183436539 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733623 | TTAATTTCAATGAAG[C/G]CCAAAACAATGTACT | 254065 |
rs183443047 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80738267 | AAAAATCGTGTTATG[G/T]ATTGTTTAATAAAAT | 254065 |
rs183449786 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80754138 | ACAATATTGTTTTTT[A/G]CAGTCCATGAGCACA | 254065 |
rs183502608 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80687242 | AAGAATTCTAGTACT[A/C]AAATCTGAACTTCAA | 254065 |
rs183510327 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80731621 | CCTTATAGGCCGGGC[A/G]CAGTGGCTCACGCCT | 254065 |
rs183513696 | snp | A/G | 2.39011e-05 | 0.00345688 | synonymous-codon, intron-variant, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80709557 | GCGTAAAGAACGCCC[A/G]CAGCTAGGCTCATAA | 254065 |
rs183517513 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80746512 | TCATGCTAAAAAACA[A/C]ATCTTGATCTCTATG | 254065 |
rs183529048 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685882 | TCTAAAATAGTGCTG[C/T]ACCTCTTCTCTGAGA | 254065 |
rs183533948 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80764046 | GAACAGAATAAAGGG[C/T]CAAAAAAATTTGCAT | 254065 |
rs183536944 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80749946 | TCACCCAAGCATTTA[A/C]AATAAAACAATATTC | 254065 |
rs183542530 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785577 | AAATACTCCAACATA[G/T]TGCAAAGTCCAGATA | 254065 |
rs183718873 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80782701 | GCCAGGAGTTTGAAA[C/T]CAGACTGGTTAACAC | 254065 |
rs183718999 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80804480 | TGACCTCAAGTGATC[C/T]GCCTGCCTCAGTCTC | 254065 |
rs183780336 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724064 | AGGGAGAGGCAAATT[A/G]CAATGGATGAAATCA | 254065 |
rs183786485 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759438 | CAGGCTTTAATTAAT[C/T]TGGGCCTCTTAAAGC | 254065 |
rs183809387 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796156 | TTTTTTTTGAGTCGG[A/G]GTCTCGCTCTGTCAC | 254065 |
rs183890474 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80746042 | CATTTTAAATATATA[A/G]GTAAATCTTTCTATA | 254065 |
rs183908673 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80781746 | AGGAAATCAAGAAAG[C/T]AATCCCATTTAGTAT | 254065 |
rs183955739 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742236 | AGATATGTGGCATTA[C/T]GTCTGAGTGCTCTGT | 254065 |
rs183969460 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80783196 | TCTAAGACCAGCCTG[A/G]CCAACGTGGTGAAAC | 254065 |
rs183981741 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80804736 | ATAAATTAGCCAACA[A/G]CTCAATAGGGTCACC | 254065 |
rs183984062 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80774214 | TTCTATCCTGACCCA[C/T]CTTTATTGAAATGCT | 254065 |
rs183995951 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726036 | TATAACATATAACAT[G/T]TTTACATGTTATGTC | 254065 |
rs183998653 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80681237 | TCTCATTAACTATAA[A/G]GATATACTAGTTTTT | 254065 |
rs184006082 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant, downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80704281 | GAATGGAGGGAGAGT[C/T]CTATACAATTTATCA | 254065 |
rs184023279 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810233 | CTCGACTCCTTTCCC[C/G]TTTTTCCTCCCGGTA | 254065 |
rs184027872 | snp | C/T | 0.0271702 | 0.113344 | intron-variant | BRWD3 | GRCh38.p7 | X:80777679 | TTGGGATTACAGGCA[C/T]GAGCCACCATGGCCG | 254065 |
rs184028883 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80761185 | GAGTGGTTATACTAA[C/T]GATACTTTATTAGTG | 254065 |
rs184042892 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80800085 | GTACACCTAATTTTG[C/T]CTAGAGGTTTAAGGG | 254065 |
rs184067645 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80763776 | TACTATGTTCATGGA[C/T]TGGAAAGTTTGACAG | 254065 |
rs184067970 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674455 | ACATGTGATCCATAT[C/T]TGGGTATATCCAGGA | 254065 |
rs184070793 | snp | A/G | 0.0699487 | 0.17344 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672386 | GGCCGAGGTGAGGAA[A/G]GAAGGAAGGAGGGAA | 254065 |
rs184074825 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | BRWD3 | GRCh38.p7 | X:80802966 | AAAAATTAGCCGGGC[A/G]TAGCGGGCGCCTGTA | 254065 |
rs184083428 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80698431 | AGTAAGAACTTGGCC[A/G]GGTGAGGTAGCTCAT | 254065 |
rs184102176 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80720143 | AATGACTATATTACT[A/G]TTTTATGTATGCACT | 254065 |
rs184108688 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80755089 | TGGTTTCTTCCTTGA[C/T]TCTGTTTATGTGATG | 254065 |
rs184111699 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80738939 | TCACTGTGAAGACTT[C/T]AGCTTTAACTCTGAG | 254065 |
rs184183704 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80699744 | AATTATGGACTAGTA[C/T]AGACTAGACAATAGA | 254065 |
rs184197175 | snp | A/G | 0.000512414 | 0.0159983 | intron-variant | BRWD3 | GRCh38.p7 | X:80696727 | AACAGAGACTCAGAG[A/G]TAACTACTCACTTAA | 254065 |
rs184204534 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80739974 | AATGATTTTTTTCAA[A/T]GGCATATGACAGTAT | 254065 |
rs184241137 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80730652 | GAATATACTAAAAAC[C/T]AATGAATTTTATGTC | 254065 |
rs184355373 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80721461 | AACATAAAAGGACGT[A/G]CAGCATTTCACTCCA | 254065 |
rs184406680 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80693724 | GAAGACATTTCTAAG[C/T]AGCAAAGGATTCAAG | 254065 |
rs184410811 | snp | A/T | | | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670063 | TATAATCTGTAGATA[A/T]GAACTTCATTAAGGC | 254065 |
rs184418471 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80736530 | TTGGGAAGTTAATAT[C/T]CAAGTATTTGGTTTT | 254065 |
rs184422973 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80714951 | GATTAAAATTTGAAG[C/T]GAAAACTATTTTATT | 254065 |
rs184426204 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80760248 | CTGGGTATTTTACCA[C/T]TGACCATAATAAACA | 254065 |
rs184428407 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80752064 | GTCGCCCAGGCTGGA[A/G]TGCAGTGGCACTATC | 254065 |
rs184466365 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | BRWD3 | GRCh38.p7 | X:80772195 | GCGGCACTATTCACA[A/G]TAGCAAAGACTTGGA | 254065 |
rs184580387 | snp | A/C | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80756531 | AAAAAAAAAAGAAAC[A/C]ATGTCAACACTCTCT | 254065 |
rs184610944 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80794497 | GAGAATGAGAGAGAC[C/T]TCGACTCAAAAAAAT | 254065 |
rs184646927 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80680090 | ATGGTTAAATAACAA[C/G/T]GGATAAGCTACTTAA | 254065 |
rs184673698 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80687557 | ATAGCAGGCCAGGAT[C/T]TGCTTGCAAGGTTGG | 254065 |
rs184705265 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80732541 | AGAAGAGGGGGAAAA[A/G]AAGAAAGGACAGGGA | 254065 |
rs184713461 | snp | A/G | 0.0714214 | 0.174956 | intron-variant | BRWD3 | GRCh38.p7 | X:80764504 | ATTTTTAGTATAGAC[A/G]GTGTTTCACCATGTT | 254065 |
rs184717788 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80791223 | TATATATAAAATAAC[G/T]TAATTTTTTAGAAGA | 254065 |
rs184792905 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80751092 | GTTACCACAGGATAC[A/G]AGGAAAGGAGAGGGG | 254065 |
rs184804572 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80787129 | AAAACTATATAAAAA[A/C]CATAAAATCCTTAGG | 254065 |
rs184828288 | snp | C/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80709702 | ATAAATTCCCCAAAA[C/T]AAAGTCAACATAGAA | 254065 |
rs184848864 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80771456 | ACACCACACATCTAC[A/C]ACCATCTGATCTTTG | 254065 |
rs184856177 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80747006 | GAGTAAATAATGGGA[G/T]GAACTGCATAAGCAT | 254065 |
rs184865914 | snp | C/G | 0.00738971 | 0.0603345 | intron-variant | BRWD3 | GRCh38.p7 | X:80686278 | TGGGGGTTGGGGGAG[C/G]GGGGAGGGATAGCAT | 254065 |
rs184887405 | snp | A/C | 0.16651 | 0.235647 | intron-variant | BRWD3 | GRCh38.p7 | X:80735753 | AGCTTGCAGTGAGCC[A/C]AGATCACACCACTGC | 254065 |
rs184895270 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768882 | AATAAAGGGAAGGAG[G/T]AAGATCTACCAAGCA | 254065 |
rs184898877 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752487 | CTCCATACTATTTAC[C/T]ACAGAGGCTGTACTT | 254065 |
rs184902639 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80767955 | CTTCAATAGCCGATT[C/T]GATCAATTGGAAGGA | 254065 |
rs184903942 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80788922 | TCACAGAAAGATTAG[C/T]GGTTTCCAGGGGTTG | 254065 |
rs184929502 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80739335 | TCTAAGGAAGAAAAA[A/T]TAGTTCAATAATGAA | 254065 |
rs184940428 | snp | A/T | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80675279 | TCCTGAAAGACTAGA[A/T]CAGAAGAACCCTTTG | 254065 |
rs184945422 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | BRWD3 | GRCh38.p7 | X:80772033 | TGGGAGTGTAAACTA[C/G]TTCAACCATTCTGGA | 254065 |
rs184947200 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80756233 | TTAAGAAATAACGTC[A/G]GCTCATGCCTGTAAT | 254065 |
rs184962244 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80714740 | AAAATTTGATTCTTC[A/G]TCAAAGGCACATAGA | 254065 |
rs184963043 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80792426 | ACAGATAACAGCACT[A/G]CATATCAGATGGTAA | 254065 |
rs184966531 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669474 | ATTTATAAATTAAAC[A/G]TACGGAAATAATTCA | 254065 |
rs185034080 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703780 | CTGCCAATAAAAAAT[C/T]ACTTTACTAAATTTT | 254065 |
rs185038191 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80743231 | TGAACCAGCCGTGCA[C/T]CCCAGGGATGAAGTC | 254065 |
rs185081878 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80692232 | ATTTTACATGACTTC[A/T]TGGGGGTGAAATTTG | 254065 |
rs185115462 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679749 | AAACTAAAAAAAGAC[A/G]CTAGTTGGCCACTGA | 254065 |
rs185154833 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80725485 | TTGTATTTTAGTAGG[A/T]CCCATGATACATTCA | 254065 |
rs185279570 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80768223 | CAAATTCAGGAAATA[A/G]AGAGACCACCACAAA | 254065 |
rs185287792 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810773 | TGAAATCTTCAATGA[C/T]GAAAGGGGTTGGTAT | 254065 |
rs185401900 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80787806 | AAGACACTGGTAGGC[C/T]GGGCGTGGTGGCTCA | 254065 |
rs185422508 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80700298 | CTTTCCCTTCAATCA[A/G]CTTCATAAGTGTGCT | 254065 |
rs185429233 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80748276 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 254065 |
rs185435732 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733258 | AGCACTCAGAAAGGA[C/T]GACCTGATAGGCTAT | 254065 |
rs185436170 | snp | G/T | 0.00844089 | 0.0644143 | intron-variant | BRWD3 | GRCh38.p7 | X:80766804 | AGTGGAAGCAGGGTG[G/T]GGCACTGCCTCACGC | 254065 |
rs185450304 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80785134 | AAGAAATAGTAATAG[A/G]TGATAGTGTAAGACC | 254065 |
rs185458217 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807169 | GACTTAAGTCCAACA[G/T]AAAGACTGACTACAA | 254065 |
rs185459191 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80740958 | GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACA | 254065 |
rs185465699 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80757096 | ATTACATTCTCACTG[C/T]TAAACTTCAAAATCT | 254065 |
rs185468888 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80773510 | TCTTATATTAGTTAC[A/G]TATTTCTGATTTAAG | 254065 |
rs185503880 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80725794 | CCTATATAACGTATA[A/G]CATGTTTACATGTGT | 254065 |
rs185509395 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80760744 | GTGATTCTTTTCTTA[C/T]TTTCTTTCTTCATTG | 254065 |
rs185533031 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80807452 | AATTTTAAATCATTT[A/T]TATTTAGAGTCTATC | 254065 |
rs185536380 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80799450 | TGTTTTCCAAGACCA[C/T]GGCTACAGAAGTTAA | 254065 |
rs185556297 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80720846 | TTTTTCTGTACCTTT[C/T]CTGTCTAGATATGCT | 254065 |
rs185616962 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80703963 | ACTATAGAATGTGTC[C/T]ATAATCAATTTTGAA | 254065 |
rs185646721 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80743812 | ATCTCACTCTATTTA[C/T]AGAACTTTTTAAATC | 254065 |
rs185661324 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776957 | TCCCTCATCCCTCTT[A/T]TCCAGAGGCCTTTCA | 254065 |
rs185696207 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80699168 | TGCAGTGAGCCGAGA[C/T]AGGGCCACTGCACTC | 254065 |
rs185734760 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80674666 | CTGAGTTACAACCAG[A/T]AGTAGTTTTGGTTTA | 254065 |
rs185752761 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80727922 | TCTAGCATGACAGGA[C/G]TCTGTCTAATTTACC | 254065 |
rs185759835 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80806151 | TCTCTTACAAAGAAG[C/T]CCATAGGTAGAGAAC | 254065 |
rs185762929 | snp | C/T | 0.000144483 | 0.00849826 | intron-variant | BRWD3 | GRCh38.p7 | X:80745777 | AAAGTGAAACTGATT[C/T]CATGAAATTAAGTCA | 254065 |
rs185783882 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80762494 | TGGATCTAAAGCGGT[A/G]AACTCCTCCTCATTT | 254065 |
rs185790212 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80781115 | CTTACTATGTAAATT[A/G]CAGGATATTGCTATA | 254065 |
rs185792323 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80802240 | GAGGTCAGGAGTTCA[A/G]GACTAGCCTTGGCCA | 254065 |
rs185967249 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80696160 | TGACCTGTTTGGGAG[C/T]GCCCTGCCTACTGCC | 254065 |
rs185974935 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80690425 | AAGAGCAAGAAAAAA[A/T]AACAGATTATAAAAA | 254065 |
rs185975704 | snp | C/T | 0.00949095 | 0.0682305 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80672284 | TAAAAGTAAGCAGGA[C/T]TGAAAAGATGAAAAA | 254065 |
rs185985551 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80717344 | GGCTATAAACTCAGA[A/G]CAGAGATAATGTTTT | 254065 |
rs185991650 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | BRWD3 | GRCh38.p7 | X:80778313 | TTAAGAAAATCCTGT[A/T]ACCAACTTCAAGACA | 254065 |
rs185991854 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80753805 | AATGCATGTTCTTGT[C/T]AGCTTTGTCAAAGAT | 254065 |
rs185997059 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | BRWD3 | GRCh38.p7 | X:80738019 | GTGACAGAGATTGTA[C/T]GACATGCTAAGCCTA | 254065 |
rs185997084 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80800568 | ATACAAATACAAATA[C/T]TTGTACAAAAAAAAA | 254065 |
rs186011864 | snp | A/T | 0.0276852 | 0.114351 | intron-variant | BRWD3 | GRCh38.p7 | X:80769884 | GAAAAGAGAGAAGAA[A/T]CAAATAGATGCAATA | 254065 |
rs186154614 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80794678 | CAGCACATTTAAATG[A/G]TATGACAACATTTAC | 254065 |
rs186158505 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80766862 | CCTTTCCTAGCCAAC[A/G]GAAGCCTTGAGAGAC | 254065 |
rs186252963 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80796659 | AATCTACCAAAATAA[G/T]TGAAGCCTGTGCAAC | 254065 |
rs186304049 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80749447 | ATCATTACATATGAC[A/G]TTTTTTGTCACTATT | 254065 |
rs186324500 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80785481 | CTCTCAAATTCCTTC[C/T]TTATGCTCCCTTACC | 254065 |
rs186335290 | snp | A/C | 4.70455e-05 | 0.0048498 | intron-variant | BRWD3 | GRCh38.p7 | X:80691020 | AGCCATAAAGCTATA[A/C]ATTTTATAATAAGTG | 254065 |
rs186338886 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80733832 | GCATTAAATTTTACA[C/T]ATAATTTTATTAATG | 254065 |
rs186343350 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80758389 | ACAAGCTCTGCAGTG[A/G]TGGTGATACTCTGCC | 254065 |
rs186349450 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80773931 | GAGTAAATTCCTTCA[C/T]AGCAACAACTGCCCT | 254065 |
rs186351386 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80795441 | TATGTATATATACAC[A/G]TATATGTATGTGTAT | 254065 |
rs186356745 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80671311 | TGACCCAAAGAATAT[C/T]TGCAATGTCTAAGAT | 254065 |
rs186391561 | snp | C/T | 0.0124979 | 0.0780562 | intron-variant | BRWD3 | GRCh38.p7 | X:80716152 | TATTGTAAAACTATA[C/T]TTACCCTTTGAGTAG | 254065 |
rs186400264 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80684410 | GTAAAGAATAGAAAA[A/T]CCATAGCCGTTGGCT | 254065 |
rs186405096 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80752954 | ATAGGCGTGAACCAC[C/T]ACGCCTGGCCGATCA | 254065 |
rs186411027 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80706447 | CTATAAGGTTTTTTC[C/T]ATTTTTAAGGTTTAA | 254065 |
rs186419868 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80736654 | TAAAATAGTTCAAAT[C/T]GTTATTCGTATCATA | 254065 |
rs186423253 | snp | C/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80726988 | TACTTCAATGTACAT[C/T]AGGGAAAAAAAAAAA | 254065 |
rs186436059 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80789412 | ACGGAGTCTCGCTCT[G/T]TCGCCCAGGCTGGAG | 254065 |
rs186453407 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80689016 | AAACAGCATTGGAGA[A/T]TTACCATTCTGGAGA | 254065 |
rs186463689 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80711459 | TAACCGCAAATATGT[C/T]TCTGTCATATCTTGA | 254065 |
rs186514559 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80713624 | ATCTGCTGACCTTCC[C/T]TCCACTATTGTCCTA | 254065 |
rs186593120 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80695106 | AGTTTTCACAAGATC[G/T]GATGGTTTAAAGGTG | 254065 |
rs186596263 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80737172 | GCCTATATAGTCCTC[C/T]GTTGGTATCATTGAG | 254065 |
rs186623465 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80769561 | AGAACAAAGATACAA[C/T]GTACCAGAATCTCTG | 254065 |
rs186643476 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80705652 | TCTATATAGGTAGAA[C/G]CTAATGCTCCAAGGC | 254065 |
rs186798572 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80735333 | GTGGTCAATAAGTAC[C/T]ATTCTCATCAATTAG | 254065 |
rs186800445 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80767823 | TTGCAAGGAAGCTAA[A/G]AACTTTGAAAAAAGA | 254065 |
rs186804875 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80750657 | AAACATTTTGGAAAA[C/T]AGTATGGAGGTTCCT | 254065 |
rs186808181 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80786938 | CTTTATTTGCAGACA[A/G]CAGGGTTATCTATAT | 254065 |
rs186822814 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810042 | AGCTCTGGGAAGGAG[A/G]GGGAGGTGCTAACTG | 254065 |
rs186863762 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80682227 | TGCCCTAAAATTCAT[G/T]AAATAGATAATTTGA | 254065 |
rs186873340 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80745059 | CTACAATTTTGTACT[A/C]AAAAGCATACAGTAT | 254065 |
rs186905189 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80702136 | AAGTAAAAAGTAATG[C/T]TGCCATTAAGAAATC | 254065 |
rs186914032 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80678843 | CAAAATTCATATGTG[A/G]AAGCCCTAATCCCCG | 254065 |
rs186981792 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80724557 | ACAACTTTCTGATTA[C/T]TAAATCATATGAGGT | 254065 |
rs186992811 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80702400 | GTGTACAGATCCTTA[C/T]ATTGTTCTATAAAGT | 254065 |
rs186993287 | snp | A/T | 0.102239 | 0.20166 | intron-variant | BRWD3 | GRCh38.p7 | X:80801213 | GGGCATGAGAAAACA[A/T]CTTTTTTTTTTTTTT | 254065 |
rs187000573 | snp | A/C | 0.0110639 | 0.0735497 | intron-variant | BRWD3 | GRCh38.p7 | X:80742928 | CCAGAACTTCCAGCA[A/C]TATGTTGAATAGGAG | 254065 |
rs187008788 | snp | C/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80775327 | ATCACAAACTCTAAG[C/G]CTTTGTTATGTCAAA | 254065 |
rs187008964 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80759965 | GATTCCTAAATGCAC[G/T]TAACATGCACTGCTA | 254065 |
rs187027616 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80798247 | GCTTCCAAACTATAT[C/T]GATGTAGTTCTTAAA | 254065 |
rs187081314 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80726297 | TATAACATATAACAC[A/G]TTTACATGTTATGTC | 254065 |
rs187088328 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80761973 | CAATATTTCTACTCA[C/T]TTACTATATCCTAAT | 254065 |
rs187127487 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80789816 | TTTACTTGACCATGG[A/T]ACTCCTTTTTTTTTT | 254065 |
rs187132496 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80694042 | GACCCAGGGCCTAGA[A/G]GGAAAAAATGGTTTC | 254065 |
rs187136909 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80679485 | TATTCTAATAGAATA[A/C]AGAGATATTTAAGCT | 254065 |
rs187176323 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | BRWD3 | GRCh38.p7 | X:80762341 | AGCAAGTTTTCCTAA[C/G]TCCTAAAAGCGATAA | 254065 |
rs187200722 | snp | A/C | | | intron-variant | BRWD3 | GRCh38.p7 | X:80780332 | AGGATTAAATGGAGA[A/C]AATACTTTTTTCATT | 254065 |
rs187216483 | snp | A/T | 2.37962e-05 | 0.00344928 | intron-variant | BRWD3 | GRCh38.p7 | X:80723708 | TTGTGAATGACACAA[A/T]CCTAAATTATACTCT | 254065 |
rs187228391 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80677509 | TAAATTTCTTCAAAA[C/T]AGAAGATATTAAAGT | 254065 |
rs187229672 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80747853 | TTTTAGGGTTTTCTA[C/G]ATATAAGATCATGTC | 254065 |
rs187230387 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80707362 | TTTACCAATTTCCTA[C/T]GAGAACATAATTTCG | 254065 |
rs187238349 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80697675 | TTTATAGGTACACAG[C/T]ATTCCATGATGTCTA | 254065 |
rs187241080 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80673732 | AGCTCACTGACTATT[C/T]ATATCTAGCATAGGA | 254065 |
rs187251310 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80783719 | AATGTGGTATTTATA[C/T]GCAATGGAATACTAT | 254065 |
rs187291927 | snp | C/T | 0.00211696 | 0.0324653 | utr-variant-3-prime | BRWD3 | GRCh38.p7 | X:80670594 | TAATTAAAAAAAAAA[C/T]TGTTTTGTAGATACG | 254065 |
rs187342820 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80715558 | CAATATACAGATCAT[A/G]TTTTGCTCCTAAATG | 254065 |
rs187384754 | snp | A/G | 0.000566961 | 0.0168273 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | BRWD3 | GRCh38.p7 | X:80745587 | AAAAATTCTTCTCCC[A/G]CTTCGGTCAAATGCT | 254065 |
rs187434599 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80701134 | ACAAGAGTTCATGTC[A/G]GAACTGGCATATTAT | 254065 |
rs187438256 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80742103 | TAAGGTATAAGGAAG[A/G]GATCCAGCTTCAGCT | 254065 |
rs187448597 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80776137 | AATTTAACAGCAAAA[A/C]TTATACATAATATCC | 254065 |
rs187451975 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80798387 | TAAGAACTCTTACCC[C/T]GAATAGTTTTTTTTT | 254065 |
rs187460746 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80766689 | CTGCAGCTCCCAGCG[C/T]GATCGATGCAGAAGA | 254065 |
rs187526376 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80790925 | AAGTTAGCAATACCA[C/T]GTTCAATGAGACTCA | 254065 |
rs187545607 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80686477 | AAGAAAAGTCATACT[A/G]GTATACTGGTTACTC | 254065 |
rs187552171 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | BRWD3 | GRCh38.p7 | X:80730752 | TAACACTTCAGTTTC[C/T]ATTTTCAGAATTTAT | 254065 |
rs187553584 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80770255 | AACTCATTTTATGAG[A/G]CCAACATCAGCTTGA | 254065 |
rs187554859 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80754262 | TCCTAGATTTTGGGG[G/T]TTTTTTTGTAGCTAT | 254065 |
rs187556584 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80709063 | TAACAAAACATGTGT[A/G]CATTATGTTGATTAG | 254065 |
rs187564437 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80746246 | TAAGGAAATCTATGA[C/T]GTTACAAATATTTTA | 254065 |
rs187567106 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80790611 | AACCAGCAGAAGTTT[A/G]AAAGTATATGCTTAG | 254065 |
rs187629288 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80698931 | AAATATACATATTCT[C/T]AGCTGGGCACGGTGG | 254065 |
rs187644775 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | BRWD3 | GRCh38.p7 | X:80720459 | TAAAAATAGAAAAAC[C/G]TTATAGCATAAGGAT | 254065 |
rs187659468 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80755353 | AACAGATAAGGTGCA[A/G]TATAGGAAATATAAA | 254065 |
rs187664741 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | BRWD3 | GRCh38.p7 | X:80739086 | TGCAGGCAGATCGGT[C/T]AGAAGTCTATTTCAA | 254065 |
rs187669364 | snp | A/G | | | intron-variant | BRWD3 | GRCh38.p7 | X:80802577 | CGGTCTCTCTATCCT[A/G]ATTTTAAAATGTAGC | 254065 |
rs187672057 | snp | A/G | 0.0199298 | 0.0978146 | intron-variant | BRWD3 | GRCh38.p7 | X:80771678 | CATCAGAGTGAACAG[A/G]CAACCTACAGAATAG | 254065 |
rs187674851 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80791552 | GGGAAACTCAGCACA[C/T]AGACATGTAAATAGA | 254065 |
rs187715803 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | BRWD3 | GRCh38.p7 | X:80669311 | ATGAAAACGACTAAC[C/T]ACATTTAGAATAAAA | 254065 |
rs187716237 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | BRWD3 | GRCh38.p7 | X:80714115 | CTAAGAGTCTGGCAT[C/T]TTTTTAAGTCCGATA | 254065 |
rs187720935 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80742253 | TCTGAGTGCTCTGTT[A/C]TGTTCCATTGGTCTA | 254065 |
rs187772000 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | BRWD3 | GRCh38.p7 | X:80771237 | ACTTTCTTCACAGAA[A/T]TGGAAAAAACTACTT | 254065 |
rs187812394 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80691600 | AAGACACTTACACAG[C/T]TACCTTCACTATTAT | 254065 |
rs187822074 | snp | G/T | 0.000183501 | 0.00957689 | intron-variant | BRWD3 | GRCh38.p7 | X:80734225 | ACATACCACCTAGAA[G/T]ATTAAAAAACAAAAC | 254065 |
rs187830330 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | BRWD3 | GRCh38.p7 | X:80750085 | TAACATGTACAAAAA[C/T]CAACTCAAAATGAAT | 254065 |
rs187841061 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | BRWD3 | GRCh38.p7 | X:80768015 | TTAATGAAATAAAGC[A/G]AAAAGTTTAGAGAAA | 254065 |
rs187848059 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | BRWD3 | GRCh38.p7 | X:80810272 | GTTTTGTTTGCTGTT[C/T]ATACTCTACCCCGTG | 254065 |
rs187993255 | snp | C/T | 2.79435e-05 | 0.00373778 | intron-variant | BRWD3 | GRCh38.p7 | X:80692059 | TTACTTTTAAAAGAA[C/T]TATAATTCATTTTTT | 254065 |
rs187999644 | snp | G/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80724218 | CATCTTAAGTTGTAA[G/T]GCAATGAAGTCTTAA | 254065 |
rs188007838 | snp | C/T | 0.0157677 | 0.0873799 | intron-variant | BRWD3 | GRCh38.p7 | X:80759625 | CCATAAAATAAAATC[C/T]ATGGGTTCTTTCCCC | 254065 |
rs188012382 | snp | A/T | | | intron-variant | BRWD3 | GRCh38.p7 | X:80685186 | GCAATACAGACACAA[A/T]TATATTGTGTAATTG | 254065 |