SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs718533 | snp | C/T | 0.494896 | 0.0502606 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130630746 | CATTAGACTTCTCAG[C/T]AGCAATCTTAGAAGC | 23504 |
rs728931 | snp | A/G | 0.392511 | 0.205404 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130603517 | GATGCAGAATCATGT[A/G]CCCAGTATGATATTT | 23504 |
rs729362 | snp | A/G | 0.431769 | 0.17164 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130692400 | TGGTTTGAGCAACCA[A/G]GAATGAAGAATGATT | 23504 |
rs729463 | snp | A/C | 0.404035 | 0.196909 | upstream-variant-2KB | RIMBP2 | GRCh38.p7 | 12:130718006 | TACCACATGGATGGA[A/C]CTTGAGAGCACCATG | 23504 |
rs731850 | snp | C/T | 0.140581 | 0.224783 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130692805 | cccatcccatcccac[C/T]tttccattctatttg | 23504 |
rs731868 | snp | A/G | 0.24019 | 0.249807 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130613074 | CCCAGCTCCCTGGCC[A/G]GCAAGGATGACTAGG | 23504 |
rs744169 | snp | A/T | 0.431621 | 0.171796 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130692557 | GGCAGCCTCCTCCCC[A/T]CTTTCCTGACTCCTA | 23504 |
rs749093 | snp | C/T | 0.371987 | 0.218218 | intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130406711 | TGCAGTGGGCCGAGG[C/T]TGCACTGCTGCACTC | 23504 |
rs750047 | snp | C/T | 0.491104 | 0.0660973 | upstream-variant-2KB, intron-variant | RIMBP2, LOC105370079 | GRCh38.p7 | 12:130636949 | CACACCTAGTAATGC[C/T]TTGGGGATGGTGTCT | 23504 |
rs753055 | snp | A/G | 0.434543 | 0.168653 | intron-variant | RIMBP2, LOC105370079 | GRCh38.p7 | 12:130637745 | CAAATAGGAAAGAGG[A/G]CATTGTTAGCAGAAG | 23504 |
rs753056 | snp | A/G | 0.434831 | 0.168337 | intron-variant | RIMBP2, LOC105370079 | GRCh38.p7 | 12:130637709 | TTACACCAGGACATC[A/G]CAGCTCTACCTCATT | 23504 |
rs756186 | snp | A/G | 0.415534 | 0.187346 | synonymous-codon, intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130399802 | AAGGCCTTTCTGCCC[A/G]TTCAGCTCCCCCTAA | 23504 |
rs869173 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130424972 | ACGCATGCTTCCCCC[C/G]CCTCGGTGCCTCCAG | 23504 |
rs869174 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, missense | RIMBP2 | GRCh38.p7 | 12:130424836 | CTGACCATAGGACCT[C/T]GGAAGGCACTTTCTG | 23504 |
rs869888 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130557683 | ATTTGTCACCGattg[C/T]tgtgtaataaattac | 23504 |
rs870597 | snp | C/G | 0.295599 | 0.245806 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130459954 | TCAACCGTTAGTTCA[C/G]GACTTGGCACAGGGT | 23504 |
rs871059 | snp | C/T | 0.119978 | 0.213528 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130460912 | AGGAGGGCATGGAAT[C/T]TCCTGTGCAGTGAGC | 23504 |
rs871145 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130478273 | ctttcttactGGGAT[C/G]CGGCTATAAATATTG | 23504 |
rs871356 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130477725 | GCGATAGGAATCTGC[C/T]GGAGCAGCGTTTCTC | 23504 |
rs871568 | snp | C/T | 0.408188 | 0.193589 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130478721 | GTAGACCTGTGTTCA[C/T]GTTTTATAACGCGAA | 23504 |
rs873148 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130425232 | TGAGGATGTAGCCCC[C/T]GGGCAGTCTCCCCTG | 23504 |
rs874619 | snp | A/G | 0.342358 | 0.232314 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130448207 | ATGTGCGTGGGCTGT[A/G]ACTGGTGATGGCCAC | 23504 |
rs883766 | snp | A/G | 0.275732 | 0.248672 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130512206 | TTTGCAGCCCAGCTC[A/G]TGCCAGGGAGTCTTG | 23504 |
rs884255 | snp | G/T | 0.472803 | 0.113397 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130477646 | ATGCCATTTCTCTAA[G/T]CATTTAGCATGAGAT | 23504 |
rs884256 | snp | C/T | 0.329783 | 0.236927 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130477432 | TTTCCCGTGGCCGGG[C/T]GACGCCTGATGGCAC | 23504 |
rs901692 | snp | C/T | 0.379158 | 0.214052 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130603765 | agcagtgtcaccaca[C/T]acatgagtcatgcac | 23504 |
rs901693 | snp | A/G | 0.37955 | 0.213815 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130603378 | ACCTGCCTTCCGAGC[A/G]CATGTGTTGAGTCCG | 23504 |
rs901694 | snp | A/C | 0.499104 | 0.0211472 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130662236 | GGTCAGTCTGGGGCA[A/C]TTCTCGCCAATGTGA | 23504 |
rs901698 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130643423 | CAGGACCATGGAAGC[A/G]CAGAGATGAAAGCCG | 23504 |
rs901699 | snp | A/G | 0.309154 | 0.242901 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130643491 | CATGGGACTGGGGAC[A/G]GGAGAGCTGTTGCCT | 23504 |
rs901701 | snp | A/G | 0.261056 | 0.249755 | upstream-variant-2KB, intron-variant | RIMBP2, LOC105370079 | GRCh38.p7 | 12:130637292 | GGACTCTACTCCCAG[A/G]GGCCTCCCATTCCAC | 23504 |
rs931371 | snp | A/G | 0.488424 | 0.0751925 | upstream-variant-2KB, intron-variant, nc-transcript-variant | RIMBP2, LOC105370079 | GRCh38.p7 | 12:130636299 | ATCTGTGTGGTGCTC[A/G]AGAGTGCCAGTAGGG | 23504 |
rs931372 | snp | A/G | 0.428484 | 0.175052 | upstream-variant-2KB, intron-variant, nc-transcript-variant | RIMBP2, LOC105370079 | GRCh38.p7 | 12:130636280 | GTGCCAGTAGGGAGG[A/G]AAGATGACATGAGAA | 23504 |
rs1011347 | snp | G/T | 0.461703 | 0.132974 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130680352 | GTGTGCCAGTCCATA[G/T]TACACGGTGCCATGG | 23504 |
rs1011348 | snp | A/C | 0.489083 | 0.0730708 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130680518 | ACACATACACACGCA[A/C]GCTTGGACATGCAAA | 23504 |
rs1032562 | snp | A/G | 0.212122 | 0.247114 | intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130404924 | ATAAAAAATGAATAC[A/G]TTTTAAAATTAAAGT | 23504 |
rs1074691 | snp | G/T | 0.109461 | 0.206758 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130653067 | ATGAGAAGGACATGA[G/T]ATTTGGGGGACCAGG | 23504 |
rs1105198 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, missense | RIMBP2 | GRCh38.p7 | 12:130424521 | TCCAGGCCGCTGTCC[A/G]GGCTCCGGGTGGCCG | 23504 |
rs1195589 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130709134 | AAGCTGTTTACACAA[C/G]TTCCCATCTTTAATT | 23504 |
rs1195590 | snp | A/G | 0 | 0 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130709174 | CAGAAGCCACGATGC[A/G]GGAGGCAGTCACCAG | 23504 |
rs1195591 | snp | C/G | 0.439641 | 0.162899 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130709677 | TGGGGTGTGTTCCTG[C/G]TCTTGGAAACCACGT | 23504 |
rs1195592 | snp | C/G | 0.498794 | 0.0245311 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130709732 | TGAGGAAACCCCCCC[C/G]CTTCCCACCCAACCC | 23504 |
rs1209607 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130708062 | ttcagccataaaaag[A/G]gatgacgctctgaca | 23504 |
rs1270170 | snp | C/T | | | downstream-variant-500B, intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130396035 | ATAACCTTACCGTTT[C/T]TGGGAGTATTTTTTT | 23504 |
rs1271637 | snp | A/C | 0 | 0 | downstream-variant-500B, intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130396053 | ATGTTTACAAAAAGC[A/C]CCATAACCTTACCGT | 23504 |
rs1271638 | snp | A/C/T | 0 | 0 | intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130402008 | AGTTCCACCCACATT[A/C/T]TACTCAGCCAGAGCA | 23504 |
rs1317474 | snp | A/G | 0.356811 | 0.226034 | intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130405851 | AGTTAAGTAATCTAG[A/G]AACTTAAATTGTTTT | 23504 |
rs1356079 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130558955 | ACTAATAAGCTTTTA[A/G]AAAAGAGGGAGAATG | 23504 |
rs1356080 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130538953 | GTGGGCCTGAGGGTG[C/G]TAAGGGTGGTAAAAC | 23504 |
rs1356081 | snp | A/G | 0.465158 | 0.127307 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130456793 | TGTACGTGTGCACAT[A/G]TGCACTGTGTGCACG | 23504 |
rs1356082 | snp | C/T | 0.464523 | 0.128375 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130456928 | GGCCGCCTCCCACTT[C/T]CACGGGAGAGCAGTG | 23504 |
rs1356083 | snp | A/C | 0.493658 | 0.0559517 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130525440 | AGAGACAAGGTCATG[A/C]TTAGAGCCTCCTAGG | 23504 |
rs1399722 | snp | C/T | 0.353587 | 0.22753 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130529088 | aagccaaatgtggtc[C/T]gtccataaagtggaa | 23504 |
rs1464108 | snp | A/C | 0.4021 | 0.198407 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130537465 | TTGGAGGCCTCCCAG[A/C]ACCCCCACATGTTTG | 23504 |
rs1464109 | snp | C/T | 0.0399052 | 0.1355 | utr-variant-5-prime, synonymous-codon | RIMBP2 | GRCh38.p7 | 12:130506741 | TGTGCATCTCAACCA[C/T]CCGCTCACCCTCGTG | 23504 |
rs1487601 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130656294 | GAGGGAAGAGGAGGA[C/G]GAAGTAGGATCTCCA | 23504 |
rs1487602 | snp | C/T | 0.498459 | 0.0277128 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130618798 | ATGGGAGACTGTGCA[C/T]GAACGGGATGGAGAA | 23504 |
rs1487603 | snp | A/G | 0.303688 | 0.244167 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130674594 | TCCTTTACCCCTCAC[A/G]TGGGTTAttttaaaa | 23504 |
rs1487604 | snp | C/T | | | intron-variant | RIMBP2 | GRCh38.p7 | 12:130674631 | TGAAATGCACACAGC[C/T]TGAAATTGACCATTT | 23504 |
rs1487605 | snp | C/T | | | intron-variant | RIMBP2 | GRCh38.p7 | 12:130674704 | GACCATCACCATTGC[C/T]TAGTTCCAAAACCTT | 23504 |
rs1487606 | snp | A/G | 0.491834 | 0.0633738 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130714927 | GTGGGGGAGGTGGTG[A/G]TTTTTTAGAGCCTTC | 23504 |
rs1487607 | snp | A/G | | | intron-variant | RIMBP2 | GRCh38.p7 | 12:130670995 | aaactcctgacttca[A/G]gtgatctgcctgcct | 23504 |
rs1487608 | snp | C/T | 0.474813 | 0.109357 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130671240 | CACAGCTTCCCACTT[C/T]CAGACTTCTGATCAA | 23504 |
rs1515384 | snp | A/G | 0.138546 | 0.223781 | utr-variant-3-prime, intron-variant | RIMBP2, PIWIL1 | GRCh38.p7 | 12:130398650 | ACGTTCTGGCCACTC[A/G]AGCCAGTGTTTGGAG | 23504 |
rs1532025 | snp | C/G | 0.444799 | 0.156695 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130621319 | CCTAACTGTAGATAT[C/G]ATAATACAATGTGGG | 23504 |
rs1532026 | snp | C/T | 0.322007 | 0.239405 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130619342 | TTTACAAAACCAACC[C/T]CTGGAGCTCAGTCAG | 23504 |
rs1533395 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130484304 | TCTTTAGAAACAGCG[C/T]GAAAGCCAGGGTGTT | 23504 |
rs1565109 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130680780 | gcgctgccacggggc[C/T]gggctgctcttgtca | 23504 |
rs1567992 | snp | C/T | | | intron-variant | RIMBP2 | GRCh38.p7 | 12:130530518 | CAATATATAGAAAAC[C/T]TTATACCAGGAAATC | 23504 |
rs1567993 | snp | G/T | 0.35207 | 0.228214 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130531162 | CCTTTCCAGATGGAT[G/T]TTTTCAGATATTTTT | 23504 |
rs1567994 | snp | C/T | 0.233235 | 0.249437 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130531262 | TTTACAAAGTACACA[C/T]ACCTGTATAACCATG | 23504 |
rs1567995 | snp | C/G | 0.493568 | 0.0563433 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130531328 | CAAAACCTCTCCCCT[C/G]CCTCCTCCCAGCTGA | 23504 |
rs1567996 | snp | C/G | 0.462582 | 0.131564 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130481376 | AAAGCGCTGTGGTTG[C/G]TGGGATATTTTGTTT | 23504 |
rs1567997 | snp | C/T | 0.084728 | 0.187577 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130564322 | TTTCCCCAGTCTTTT[C/T]AGCACTGTGTTTTTT | 23504 |
rs1806564 | snp | A/G | 0.367297 | 0.220775 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130512574 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 23504 |
rs1809607 | snp | A/C | 0.499121 | 0.020948 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130662403 | tggctcacgcctgta[A/C]tcctagcacttttgg | 23504 |
rs1809608 | snp | C/T | 0.499104 | 0.0211472 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130662439 | gaggcgtgtggatga[C/T]gaggtcaagagatcg | 23504 |
rs1809609 | snp | A/G | 0.499104 | 0.0211472 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130662477 | cctggccaacatggt[A/G]aaaccccatctctac | 23504 |
rs1828945 | snp | A/G | 0 | 0 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130552861 | CCGGCGACCTGTCCT[A/G]TTTTCTCTGAGATAA | 23504 |
rs1877973 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130476029 | ATCTATGTGAGGTCA[C/T]GAGACAGTGAGTATA | 23504 |
rs1877974 | snp | G/T | 0.122758 | 0.215196 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130460017 | AAGCTGCGGGTAAAC[G/T]AATCTACGCACAGGA | 23504 |
rs1877975 | snp | A/G | 0.211516 | 0.24702 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130460209 | GGTTCCCTCTCCCAC[A/G]GGGAACCCTCAGCTC | 23504 |
rs1877976 | snp | C/T | 0.406296 | 0.19512 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130462234 | CCTGGGCCTGGGGGG[C/T]TCTGGAACTTAGAAT | 23504 |
rs1877977 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130462362 | GGTGGCCAGTGCAGA[C/T]ACCAGGAAGGCCGCG | 23504 |
rs1877978 | snp | A/G | 0.485664 | 0.0834419 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130500637 | ACTGAAAATTAGCCC[A/G]CTGGTCACATTCATA | 23504 |
rs1877979 | snp | C/T | 0.48666 | 0.0805725 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130500271 | GGGGTTTCCCCGTGT[C/T]GGTCAGGCTGGTCTC | 23504 |
rs1877980 | snp | C/T | 0.486855 | 0.0799975 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130541390 | TTCTCTCCAGTCTGA[C/T]GCTGAGGCATTTTGG | 23504 |
rs1877981 | snp | A/C | 0.488424 | 0.0751925 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130541399 | GTCTGATGCTGAGGC[A/C]TTTTGGAATGTTTCT | 23504 |
rs1877982 | snp | C/T | 0.173965 | 0.238157 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130573843 | GGGATGGGATTTCTG[C/T]GTGGACAGCCATGCT | 23504 |
rs1877983 | snp | C/T | 0.246769 | 0.249979 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130573223 | TAAAAATATAATATA[C/T]ATGAAGTATGCAATA | 23504 |
rs1877986 | snp | A/G | 0.461037 | 0.134028 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130497627 | TCTACTGCCTGATAC[A/G]CAAGACATTCTGGGT | 23504 |
rs1877987 | snp | C/T | 0.155987 | 0.23165 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130504398 | AGCAAATCAGGTTGA[C/T]TGAAACTCTGTTGAG | 23504 |
rs1877988 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130438099 | TCAAGAATGTTCTGA[C/T]ACTAGGGGTCCCCTC | 23504 |
rs1877989 | snp | A/G | 0.352287 | 0.228117 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130531462 | CTGGATATTTATCTC[A/G]ACATTTTATCTAGGA | 23504 |
rs1877990 | snp | C/G | 0.483563 | 0.0891524 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130430332 | TGGATGCGGGGCTCA[C/G]CACCTCCCCTATCCC | 23504 |
rs1877991 | snp | C/G | | | intron-variant, missense | RIMBP2 | GRCh38.p7 | 12:130424530 | TCAGCCGCTCGGCCA[C/G]CCGGAGCCCGGACAG | 23504 |
rs1881061 | snp | C/T | 0.433818 | 0.169443 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130712656 | tagaaacaatacact[C/T]taaaatcatgataaa | 23504 |
rs1881062 | snp | C/T | 0.457969 | 0.138741 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130701687 | CCATGGGACACAAAT[C/T]GCTCCTGCTTGACAG | 23504 |
rs1881066 | snp | C/G | 0.224709 | 0.248717 | upstream-variant-2KB | RIMBP2 | GRCh38.p7 | 12:130717945 | CATATCCATACAATG[C/G]AATATTATTCAGCCA | 23504 |
rs1918561 | snp | C/T | 0.159292 | 0.232964 | intron-variant | RIMBP2 | GRCh38.p7 | 12:130714804 | GGGAGCTTGGGATCA[C/T]GTCTCACAGGACAAG | 23504 |