SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1671 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192643 | TATATCAACTTACTA[C/T]TCATGAAAAGAATGG | 54014 |
rs3945 | snp | A/G | 0.259397 | 0.249823 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39194141 | TTGGATGGCCAGTCA[A/G]TGACCAATTAATGCA | 54014 |
rs13625 | snp | G/T | 0.337386 | 0.23423 | utr-variant-3-prime, intron-variant | BRWD1 | GRCh38.p7 | 21:39297157 | CTATAGGAGATAGCA[G/T]CAGAACATAGGTTTG | 54014 |
rs718225 | snp | C/G | 0.257732 | 0.24988 | intron-variant | BRWD1 | GRCh38.p7 | 21:39280690 | TCTAAGACTTAAGTA[C/G]AATTAAGGTATTATC | 54014 |
rs719230 | snp | A/G | 0.474813 | 0.109357 | intron-variant | BRWD1 | GRCh38.p7 | 21:39304381 | tcaggcagtcctccc[A/G]ccttggcttcccaaa | 54014 |
rs914157 | snp | A/T | 0.253824 | 0.249971 | intron-variant | BRWD1 | GRCh38.p7 | 21:39243927 | TTCTTAGAACTTTCA[A/T]GTCTGAAATTACATC | 54014 |
rs914158 | snp | A/G | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39244060 | GGGTTTCTGCTCTGA[A/G]ATCATGCTGCTAACt | 54014 |
rs971229 | snp | A/G | 0.244205 | 0.249933 | intron-variant | BRWD1 | GRCh38.p7 | 21:39280456 | GCCTATTTTCAGAAT[A/G]AACAAGACTGGCCAG | 54014 |
rs973521 | snp | A/G | 0.186493 | 0.241804 | intron-variant | BRWD1 | GRCh38.p7 | 21:39278695 | AGTGGTCATTTAATA[A/G]ATGTTTAAAAAAAAA | 54014 |
rs1011413 | snp | A/G | 0.472989 | 0.113031 | intron-variant | BRWD1 | GRCh38.p7 | 21:39266315 | GTGtatatatattat[A/G]tattttttttCCTCC | 54014 |
rs1029004 | snp | A/G | 0.499368 | 0.0177603 | intron-variant | BRWD1 | GRCh38.p7 | 21:39243417 | agatctgcagatctg[A/G]taatgacattatatt | 54014 |
rs1041439 | snp | A/G | 0.184884 | 0.241371 | missense | BRWD1 | GRCh38.p7 | 21:39199320 | CTGGACACTGGTAAT[A/G]GTTGATTTTCATCTT | 54014 |
rs1041440 | snp | C/T | 0.331874 | 0.236213 | intron-variant | BRWD1 | GRCh38.p7 | 21:39255399 | cctgcgcaacgagag[C/T]gaaactccgtctcga | 54014 |
rs1046284 | snp | C/T | | | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192831 | TTGAACTTGATTGTG[C/T]CAACTGAAACCCCAG | 54014 |
rs1046285 | snp | C/T | | | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192818 | TGCCAACTGAAACCC[C/T]AGAGGTTTGTATATC | 54014 |
rs1046286 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192807 | ACCCCAGAGGTTTGT[A/G]TATCAGTAGAATGCA | 54014 |
rs1046289 | snp | A/G | 0.178144 | 0.239451 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192768 | GTTAAAGGTGCTTAC[A/G]ATCTTTTTTGTTTTC | 54014 |
rs1046293 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192599 | TATCTTGCAGTTGTC[A/C]CCAAATACTGTAGTT | 54014 |
rs1065242 | snp | C/G | 0.333491 | 0.235646 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39195790 | ACTATAATCATGGGA[C/G]GTGTAACCATGATTA | 54014 |
rs1541100 | snp | C/T | 0.253824 | 0.249971 | intron-variant | BRWD1 | GRCh38.p7 | 21:39269126 | ATAGACCTGACTAGA[C/T]AATGCTATCTTATAA | 54014 |
rs1541101 | snp | C/T | 0.24449 | 0.249939 | intron-variant, utr-variant-5-prime | BRWD1 | GRCh38.p7 | 21:39232004 | TACAAATTTTGCCCA[C/T]TGACAAACAAGCCAT | 54014 |
rs1541102 | snp | C/T | 0.33533 | 0.234987 | intron-variant | BRWD1 | GRCh38.p7 | 21:39256839 | GCCTAGGGAAAAATC[C/T]ACGAGTGAATGCAAC | 54014 |
rs1888486 | snp | A/G | 0.254105 | 0.249966 | | | GRCh38.p7 | 21:39311219 | ATCTCCCAGGCTGGA[A/G]TGCAGTGGCAGGAGG | 54014 |
rs1888487 | snp | A/G | 0.474453 | 0.110094 | | | GRCh38.p7 | 21:39311333 | CCACCACAGCCGCCT[A/G]ATTTTCTGTTACTTA | 54014 |
rs1888488 | snp | C/T | 0.466927 | 0.124269 | | | GRCh38.p7 | 21:39314595 | TGTCTTGCCAGGCTT[C/T]TGACCTAACTATGAG | 54014 |
rs1963742 | snp | C/T | 0.252983 | 0.249982 | intron-variant | BRWD1 | GRCh38.p7 | 21:39244299 | ttgatctcctgccct[C/T]gtgatccacccacct | 54014 |
rs1984022 | snp | A/G | 0.332568 | 0.235971 | intron-variant, downstream-variant-500B | BRWD1 | GRCh38.p7 | 21:39224159 | ccagccAGGAGTTAA[A/G]TTTAATGCAGGGTTA | 54014 |
rs1984748 | snp | A/G | 0.245346 | 0.249957 | utr-variant-3-prime, intron-variant | BRWD1 | GRCh38.p7 | 21:39297972 | AAAAAGAACCATGCA[A/G]TTTTACATTTGTGGT | 54014 |
rs2026265 | snp | A/G | 0.332568 | 0.235971 | intron-variant | BRWD1 | GRCh38.p7 | 21:39223591 | TGGAGAAAGGTAGGA[A/G]GAAATTAAAATTGTT | 54014 |
rs2026266 | snp | C/T | 0.252702 | 0.249985 | intron-variant | BRWD1 | GRCh38.p7 | 21:39227794 | AAATCTGAAATTACT[C/T]TTCAACCTTCTGATC | 54014 |
rs2056844 | snp | C/G | 0.499533 | 0.0158644 | missense, utr-variant-5-prime, nc-transcript-variant | BRWD1 | GRCh38.p7 | 21:39298534 | TAGGACCGATGCGCT[C/G]GCAGATTTGCAAAAG | 54014 |
rs2065310 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRWD1 | GRCh38.p7 | 21:39203435 | cagagcaagaccctg[G/T]ttctttttttttttt | 54014 |
rs2065311 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | BRWD1 | GRCh38.p7 | 21:39238237 | ACCAAGATTAAATTT[A/G]TATTTTCAGTATGCA | 54014 |
rs2065312 | snp | G/T | 0 | 0 | intron-variant | BRWD1 | GRCh38.p7 | 21:39238348 | GTTGGATCTAGTTTT[G/T]GTCTCCTTTTAAGTG | 54014 |
rs2142117 | snp | C/T | 0.254105 | 0.249966 | utr-variant-3-prime, intron-variant | BRWD1 | GRCh38.p7 | 21:39297379 | AACAAACAGAGAATA[C/T]GCCCCTACCCTAGGG | 54014 |
rs2150410 | snp | A/G | 0.251578 | 0.249995 | intron-variant | BRWD1 | GRCh38.p7 | 21:39197853 | ACTTCACTAAGCAAT[A/G]GAAATTTTTAACCTT | 54014 |
rs2150411 | snp | G/T | 0.499265 | 0.0191552 | intron-variant | BRWD1 | GRCh38.p7 | 21:39202626 | AATGACTAAATAGAA[G/T]TATATCATATTTCTT | 54014 |
rs2150412 | snp | C/T | 0.252702 | 0.249985 | intron-variant | BRWD1 | GRCh38.p7 | 21:39202743 | ACTCTAAATTTAACG[C/T]ACTGTTATTCAAATT | 54014 |
rs2150413 | snp | C/T | 0.497586 | 0.0346604 | intron-variant | BRWD1 | GRCh38.p7 | 21:39242952 | ggacaatagacctag[C/T]catccaagacctctg | 54014 |
rs2150414 | snp | A/G | 0.497359 | 0.0362457 | intron-variant | BRWD1 | GRCh38.p7 | 21:39243062 | taaatccaacaatca[A/G]gactgtaattttacc | 54014 |
rs2150415 | snp | C/T | 0.332106 | 0.236133 | intron-variant | BRWD1 | GRCh38.p7 | 21:39243441 | ttatattgttgttta[C/T]tgcctcattttttgt | 54014 |
rs2178838 | snp | G/T | 0.185272 | 0.24356 | intron-variant | BRWD1 | GRCh38.p7 | 21:39274969 | CGCTTGAACCCAGGA[G/T]GGGGAGGTTGCAGTG | 54014 |
rs2183573 | snp | A/G | 0.471412 | 0.116088 | missense | BRWD1 | GRCh38.p7 | 21:39202379 | TCCTCCTTTCTGATG[A/G]TTCTGCTGAATCTGA | 54014 |
rs2183574 | snp | C/T | 0.252983 | 0.249982 | intron-variant | BRWD1 | GRCh38.p7 | 21:39222021 | aaaggcaaatcgaaa[C/T]cacaataatacttcc | 54014 |
rs2183575 | snp | A/G | 0.252983 | 0.249982 | intron-variant | BRWD1 | GRCh38.p7 | 21:39222434 | tccacagctgaggta[A/G]ggaaagtacaaggtg | 54014 |
rs2183576 | snp | C/T | 0.253824 | 0.249971 | intron-variant | BRWD1 | GRCh38.p7 | 21:39227299 | GAACTGATAAAAGAA[C/T]GAACCATCCTACTTC | 54014 |
rs2225425 | snp | C/T | 0.252983 | 0.249982 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39190204 | CTAGTTTCTACATTT[C/T]AAGGATTAATCATAT | 54014 |
rs2234543 | snp | C/T | 0.333952 | 0.235483 | intron-variant | BRWD1 | GRCh38.p7 | 21:39200146 | AATTGAATAGATTCT[C/T]GATTTAATGCATCTA | 54014 |
rs2234545 | snp | A/G | 0.178465 | 0.239547 | intron-variant | BRWD1 | GRCh38.p7 | 21:39199919 | ACTAAAAATACAAAA[A/G]ATTAGCCAGGCATGG | 54014 |
rs2234546 | snp | C/T | 0.0022078 | 0.0331516 | synonymous-codon | BRWD1 | GRCh38.p7 | 21:39199637 | ATTAGCAAATGGATG[C/T]GGCAGAAAAGCCACT | 54014 |
rs2234547 | snp | C/G | 0.000972065 | 0.0220247 | missense | BRWD1 | GRCh38.p7 | 21:39198904 | GAAGATGGGAAATGT[C/G]ATAAAATGGAAATGA | 54014 |
rs2234548 | snp | A/G | 0.0032118 | 0.0399448 | missense | BRWD1 | GRCh38.p7 | 21:39196602 | CTGATACTAGTTCCA[A/G]ATCATCAGATTTGGG | 54014 |
rs2236437 | snp | C/T | 0.257732 | 0.24988 | upstream-variant-2KB, utr-variant-3-prime | PSMG1, BRWD1 | GRCh38.p7 | 21:39184669 | TACATAAAATTAGTA[C/T]TTAGCAGATGTACAC | 54014 |
rs2272576 | snp | C/G | 0.264084 | 0.249603 | intron-variant, upstream-variant-2KB | BRWD1, BRWD1-IT2 | GRCh38.p7 | 21:39312463 | GCGGGGCAAGAGCAG[C/G]GAGGCCAATCAGAGC | 54014 |
rs2272577 | snp | C/T | 0.263809 | 0.249618 | intron-variant, upstream-variant-2KB | BRWD1, BRWD1-IT2 | GRCh38.p7 | 21:39312501 | ACAAGCGCGGTGGAG[C/T]GGGGAAGCGAATGAA | 54014 |
rs2272578 | snp | C/G | 0.288646 | 0.246995 | intron-variant, upstream-variant-2KB | BRWD1, BRWD1-IT2 | GRCh38.p7 | 21:39312715 | CGGGAACGCAGCTAT[C/G]CCCGGGCCGCCCCCC | 54014 |
rs2297255 | snp | C/G | 0.178785 | 0.239642 | utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39186052 | ATTAAAGTTTGTTGG[C/G]ATGAGATTGTAGTAA | 54014 |
rs2297256 | snp | A/G | 0.499354 | 0.0179596 | utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39186495 | TTGGGGATGTGAATT[A/G]TAGGGAATGGATCTG | 54014 |
rs2297257 | snp | A/T | 0.251859 | 0.249993 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39190239 | ATTAGACTTTTTTTT[A/T]ATTTTTAAGCTACCT | 54014 |
rs2297258 | snp | C/G | 0.191064 | 0.24296 | intron-variant, upstream-variant-2KB | BRWD1, BRWD1-IT2 | GRCh38.p7 | 21:39312935 | ACACGAGTGACCACC[C/G]CTCCGGCGCGGGGGG | 54014 |
rs2410104 | snp | C/T | 0.251014 | 0.249998 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192538 | TGACTTGTTGCACTC[C/T]ATCACATTAAAATAA | 54014 |
rs2410105 | snp | A/C | 0 | 0 | intron-variant | BRWD1 | GRCh38.p7 | 21:39204121 | gcacaacaacacact[A/C]cagcctggacaacaa | 54014 |
rs2410106 | snp | C/T | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39217024 | AAatatatatatata[C/T]atatatatataaata | 54014 |
rs2410121 | snp | C/T | 0.253824 | 0.249971 | intron-variant | BRWD1 | GRCh38.p7 | 21:39268331 | tgtaaatcccagcta[C/T]tcgggaggctgaggc | 54014 |
rs2410122 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | BRWD1 | GRCh38.p7 | 21:39282845 | gcgcctgtaatccca[A/G]ctactcgggaggctg | 54014 |
rs2471953 | snp | A/G | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39271799 | tcccagcacttttga[A/G]aggccaaggtgggcg | 54014 |
rs2471955 | snp | C/G | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39212967 | AGCTATAAAAAGACG[C/G]TTCATGCATTTCCTA | 54014 |
rs2471956 | snp | C/T | 0 | 0 | intron-variant | BRWD1 | GRCh38.p7 | 21:39217969 | AATATGGTAGTCAAT[C/T]TTCTGCCTGGCCCTA | 54014 |
rs2471957 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | BRWD1 | GRCh38.p7 | 21:39228324 | CCCTACCAAGAAAGT[C/T]TGCATAATCAGTAAG | 54014 |
rs2471958 | snp | C/T | | | intron-variant, downstream-variant-500B | BRWD1 | GRCh38.p7 | 21:39228383 | AGGTCACTTATATCT[C/T]TTCTGGAATTTACAT | 54014 |
rs2471959 | snp | A/T | 0 | 0 | intron-variant | BRWD1 | GRCh38.p7 | 21:39253317 | aaaaaaaaaaGGACT[A/T]GAAGCCAAGCTCCAC | 54014 |
rs2481861 | snp | A/T | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39271723 | AAAAAAAAAAAAGAT[A/T]TTACAAGCATCTAAC | 54014 |
rs2481862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRWD1 | GRCh38.p7 | 21:39286078 | agagtgcagtggtgc[A/G]atctcggctcactgc | 54014 |
rs2481863 | snp | A/G | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39286358 | attcagtggcattta[A/G]tacatgcacaatgct | 54014 |
rs2481864 | snp | C/T | 0 | 0 | intron-variant | BRWD1 | GRCh38.p7 | 21:39301881 | AAGGCAGTAGAACAT[C/T]TTTACTGTGCCGAAA | 54014 |
rs2481865 | snp | C/T | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39304097 | agtgagccgagattt[C/T]gccattgcactccag | 54014 |
rs2481866 | snp | C/G | | | utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39186694 | TTCAAGTTCTTCCTA[C/G]CCTGTACACTTCCCA | 54014 |
rs2481867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BRWD1 | GRCh38.p7 | 21:39203209 | taatcccagcacttt[A/G]ggaggccaaggcagg | 54014 |
rs2481869 | snp | A/C | | | intron-variant | BRWD1 | GRCh38.p7 | 21:39248267 | tcattagagaaatgc[A/C]aatcaaaaccacaat | 54014 |
rs2836933 | snp | C/G | 0.335559 | 0.234904 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192276 | ACTTTTCAATCCTTA[C/G]TATTCACAGTTTGAG | 54014 |
rs2836934 | snp | A/C | 0.499035 | 0.0219437 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39192959 | TAGAAGACAGAGGGA[A/C]TGTAGTGTGCACCCC | 54014 |
rs2836935 | snp | G/T | 0.237593 | 0.249692 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39194446 | TTAGTCAAGGACAAT[G/T]ATCATGAATCAATCT | 54014 |
rs2836936 | snp | A/G | 0.177503 | 0.239258 | intron-variant, utr-variant-3-prime | BRWD1 | GRCh38.p7 | 21:39195426 | TAAGATTATGGAAGA[A/G]CAAGATTTTGGTTAA | 54014 |
rs2836937 | snp | C/T | 0.17461 | 0.238362 | intron-variant | BRWD1 | GRCh38.p7 | 21:39201973 | ACCAGATGGCAACAA[C/T]ATGAACAGTTTAGAA | 54014 |
rs2836938 | snp | C/T | 0.331411 | 0.236373 | intron-variant | BRWD1 | GRCh38.p7 | 21:39202265 | CTAAATCTCTAGTAA[C/T]GGCCAGTGTTACACA | 54014 |
rs2836939 | snp | A/G | 0.161596 | 0.233848 | intron-variant | BRWD1 | GRCh38.p7 | 21:39206620 | GATGGGAAGTTGAAT[A/G]GTTTTAAGGCTGCTA | 54014 |
rs2836940 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | BRWD1 | GRCh38.p7 | 21:39216770 | CACCTGTTCAGACCA[C/T]TGCTTACAGAAATAT | 54014 |
rs2836941 | snp | C/T | 0.176219 | 0.238865 | intron-variant | BRWD1 | GRCh38.p7 | 21:39218973 | ACAAATTGAACCTGA[C/T]AATATTCAAAATTTT | 54014 |
rs2836942 | snp | A/G | 0.49928 | 0.018956 | intron-variant | BRWD1 | GRCh38.p7 | 21:39219455 | ATCTGAGGAAGCTCA[A/G]AATATTTTAGCTTAT | 54014 |
rs2836943 | snp | C/T | 0.499 | 0.0223418 | intron-variant | BRWD1 | GRCh38.p7 | 21:39220685 | gcaaagacatgaatg[C/T]agttattatattacg | 54014 |
rs2836944 | snp | A/G | 0.335559 | 0.234904 | intron-variant | BRWD1 | GRCh38.p7 | 21:39221613 | ATATCCCAAACTAAT[A/G]GATAACAGTTaaaaa | 54014 |
rs2836945 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | BRWD1 | GRCh38.p7 | 21:39224831 | GAACTAGGACACTGA[C/T]AATACGAGGTAAAGG | 54014 |
rs2836946 | snp | A/G | 0.234109 | 0.249494 | intron-variant | BRWD1 | GRCh38.p7 | 21:39224837 | GGACACTGACAATAC[A/G]AGGTAAAGGAAATAT | 54014 |
rs2836947 | snp | G/T | 0.17654 | 0.238964 | intron-variant | BRWD1 | GRCh38.p7 | 21:39226450 | AACCACTAAATTACA[G/T]GAGGCATCTGGGACT | 54014 |
rs2836948 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | BRWD1 | GRCh38.p7 | 21:39227751 | TCAAGGGTAAAATAA[C/T]TGGGTATACCAGAAC | 54014 |
rs2836949 | snp | A/C | 0.495745 | 0.0459295 | intron-variant, utr-variant-5-prime | BRWD1 | GRCh38.p7 | 21:39230530 | GTAAACCAGTGCATA[A/C]GTAACTTGGTTTTAT | 54014 |
rs2836950 | snp | C/G | 0.46523 | 0.127207 | intron-variant, upstream-variant-2KB | BRWD1 | GRCh38.p7 | 21:39232503 | CTCCGCAAATTCTAC[C/G]AAGGGGAAGAGAACA | 54014 |
rs2836951 | snp | A/G | 0.42 | 0.183303 | intron-variant | BRWD1 | GRCh38.p7 | 21:39238860 | GTTAATAAAAAGTCA[A/G]TGTAAATGTTTTCCA | 54014 |
rs2836952 | snp | C/G | 0.498832 | 0.0241331 | intron-variant | BRWD1 | GRCh38.p7 | 21:39244725 | ATGTCTACTGTGTTG[C/G]GCAAATTCAAGGTAC | 54014 |
rs2836953 | snp | A/G | 0.352287 | 0.228117 | intron-variant | BRWD1 | GRCh38.p7 | 21:39245557 | TCAAAACATTACTCA[A/G]TCAGGAAATTTTAAC | 54014 |