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 |